WorldWideScience

Sample records for highly selective ion

  1. A Novel Ion - selective Polymeric Membrane Sensor for Determining Thallium(I) With High Selectivity

    Science.gov (United States)

    Kassim, Anuar; Rezayi, Majid; Ahmadzadeh, Saeid; Rounaghi, Gholamhossein; Mohajeri, Masoomeh; Azah Yusof, Noor; Tee, Tan Wee; Yook Heng, Lee; Halim Abdullah, Abd

    2011-02-01

    Thallium is a toxic metal that introduced into the environment mainly as a waste from the production of zinc, cadmium, and lead and by combustion of coal. Thallium causes gastrointestinal irritation and nerve damage when people are exposed to it for relatively short period of time. For long term, thallium has the potential to cause the following effects: change in blood chemistry, damage to liver, kidney, intestinal and testicular tissue, and hair loss. In this work a membrane was prepared by use of 4'-nitrobenzo -18-crown-6 (4'NB18C6) as an ion carrier, polyvinylchloride (PVC) as a matrix, and diocthylphetalate (DOP) as a plasticizer for making an ion selective electrode for measurement of Tl+ cation in solutions. The amount of 4'-nitrobenzo-18C6 and polyvinylchloride were optimized in the preparation of the membrane. The response of the electrode was Nernstian within the concentration range 1.0 × 10-8 to 1.0 × 10-1M. This sensor displays a drift in Nernstian response for this cation with increasing the amount of ionophore and decreasing the amount of polyvinylchloride.The results of potentiometric measurements showed that, this electrode also responses to Cu2+ Ni2+ and Pb2+ cations, but the electrode has a wider dynamic range and a lower detection limit to Tl+ cation. The effects of various parameters such as pH, different cations interferences, effect of the amount of ionophore and polyvinylchloride and time on response of the coated ion selective electrode were investigated. Finally the constructed electrode was used in complexometric and precipitation titrations of Tl+ cation with EDTA and KBr, respectively. The response of the fabricated electrode at concentration range from 1.0 × 10-8 to 1.0 × 10-1M is linear with a Nernstian slope of 57.27 mV.

  2. Ultrathin and Ion-Selective Janus Membranes for High-Performance Osmotic Energy Conversion.

    Science.gov (United States)

    Zhang, Zhen; Sui, Xin; Li, Pei; Xie, Ganhua; Kong, Xiang-Yu; Xiao, Kai; Gao, Longcheng; Wen, Liping; Jiang, Lei

    2017-07-05

    The osmotic energy existing in fluids is recognized as a promising "blue" energy source that can help solve the global issues of energy shortage and environmental pollution. Recently, nanofluidic channels have shown great potential for capturing this worldwide energy because of their novel transport properties contributed by nanoconfinement. However, with respect to membrane-scale porous systems, high resistance and undesirable ion selectivity remain bottlenecks, impeding their applications. The development of thinner, low-resistance membranes, meanwhile promoting their ion selectivity, is a necessity. Here, we engineered ultrathin and ion-selective Janus membranes prepared via the phase separation of two block copolymers, which enable osmotic energy conversion with power densities of approximately 2.04 W/m 2 by mixing natural seawater and river water. Both experiments and continuum simulation help us to understand the mechanism for how membrane thickness and channel structure dominate the ion transport process and overall device performance, which can serve as a general guiding principle for the future design of nanochannel membranes for high-energy concentration cells.

  3. Synthesis and application of a highly selective copper ions fluorescent probe based on the coumarin group

    Science.gov (United States)

    He, Guangjie; Liu, Xiangli; Xu, Jinhe; Ji, Liguo; Yang, Linlin; Fan, Aiying; Wang, Songjun; Wang, Qingzhi

    2018-02-01

    A highly selective copper ions fluorescent probe based on the coumarin-type Schiff base derivative 1 (probe) was produced by condensation reaction between coumarin carbohydrazide and 1H-indazole-3-carbaldehyde. The UV-vis spectroscopy showed that the maximum absorption peak of compound 1 appeared at 439 nm. In the presence of Cu2 + ions, the maximum peak decreased remarkably compared with other physiological important metal ions and a new absorption peak at 500 nm appeared. The job's plot experiments showed that complexes of 1:2 binding mode were formed in CH3CN:HEPES (3:2, v/v) solution. Compound 1 exhibited a strong blue fluorescence. Upon addition of copper ions, the fluorescence gradually decreased and reached a plateau with the fluorescence quenching rate up to 98.73%. The detection limit for Cu2 + ions was estimated to 0.384 ppm. Fluorescent microscopy experiments demonstrated that probe 1 had potential to be used to investigate biological processes involving Cu2 + ions within living cells.

  4. Ultrasensitive and highly selective detection of Cu2 + ions based on a new carbazole-Schiff

    Science.gov (United States)

    Yin, Jun; Bing, Qijing; Wang, Lin; Wang, Guang

    2018-01-01

    A new chemosensor for Cu2 + based on Schiff base with high sensitivity and selectivity was designed and synthesized. The fluorescence intensity of the chemosensor in CH3CN solution was enhanced 160-fold after the addition of 10 equiv. Cu2 + over other metal ions. In addition, it also facilitates colorimetric detection for Cu2 + in CH3CN solution. The chemosensor displayed low detection limit and fast response time to Cu2 +.

  5. First state selective electron capture measurements with trapped highly charged ions

    NARCIS (Netherlands)

    Bliek, F.W.; Woestenenk, G.R.; Hoekstra, R.A.; Morgenstern, R.W.H.

    1997-01-01

    The first state selective electron capture cross section measurements at eV energies are reported for collisions between C4+ ions and H-2 molecules. The cross sections are measured in a crossed beam experiment by means of Photon Emission Spectroscopy. The ion beams are decelerated in an octopole ion

  6. Highly Sensitive and Selective Detection of Nanomolar Ferric Ions Using Dopamine Functionalized Graphene Quantum Dots.

    Science.gov (United States)

    Dutta Chowdhury, Ankan; Doong, Ruey-An

    2016-08-17

    The good stability, low cytotoxicity, and excellent photoluminescence property of graphene quantum dots (GQDs) make them an emerging class of promising materials in various application fields ranging from sensor to drug delivery. In the present work, the dopamine-functionalized GQDs (DA-GQDs) with stably bright blue fluorescence were successfully synthesized for low level Fe(3+) ions detection. The as-synthesized GQDs are uniform in size with narrow-distributed particle size of 4.5 ± 0.6 nm and high quantum yield of 10.2%. The amide linkage of GQDs with dopamine, confirmed by using XPS and FTIR spectra, results in the specific interaction between Fe(3+) and catechol moiety of dopamine at the interfaces for highly sensitive and selective detection of Fe(3+). A linear range of 20 nM to 2 μM with a detection limit of 7.6 nM is obtained for Fe(3+) detection by DA-GQDs. The selectivity of DA-GQDs sensing probe is significantly excellent in the presence of other interfering metal ions. In addition, the reaction mechanism for Fe(3+) detection based on the complexation and oxidation of dopamine has been proposed and validated. Results obtained in this study clearly demonstrate the superiority of surface functionalized GQDs to Fe(3+) detection, which can pave an avenue for the development of high performance and robust sensing probes for detection of metal ions and other organic metabolites in environmental and biomedical applications.

  7. Miniaturizable Ion-Selective Arrays Based on Highly Stable Polymer Membranes for Biomedical Applications

    Directory of Open Access Journals (Sweden)

    Mònica Mir

    2014-07-01

    Full Text Available Poly(vinylchloride (PVC is the most common polymer matrix used in the fabrication of ion-selective electrodes (ISEs. However, the surfaces of PVC-based sensors have been reported to show membrane instability. In an attempt to overcome this limitation, here we developed two alternative methods for the preparation of highly stable and robust ion-selective sensors. These platforms are based on the selective electropolymerization of poly(3,4-ethylenedioxythiophene (PEDOT, where the sulfur atoms contained in the polymer covalently interact with the gold electrode, also permitting controlled selective attachment on a miniaturized electrode in an array format. This platform sensor was improved with the crosslinking of the membrane compounds with poly(ethyleneglycol diglycidyl ether (PEG, thus also increasing the biocompatibility of the sensor. The resulting ISE membranes showed faster signal stabilization of the sensor response compared with that of the PVC matrix and also better reproducibility and stability, thus making these platforms highly suitable candidates for the manufacture of robust implantable sensors.

  8. Pure zinc sulfide quantum dot as highly selective luminescent probe for determination of hazardous cyanide ion

    Energy Technology Data Exchange (ETDEWEB)

    Shamsipur, Mojtaba, E-mail: mshamsipur@yahoo.com [Department of Chemistry, Razi University, Kermanshah (Iran, Islamic Republic of); Rajabi, Hamid Reza, E-mail: h.rajabi@mail.yu.ac.ir [Chemistry Department, Yasouj University, Yasouj 75918-74831 (Iran, Islamic Republic of)

    2014-03-01

    A rapid and simple fluorescence method is presented for selective and sensitive determination of hazardous cyanide ion in aqueous solution based on functionalized zinc sulfide (ZnS) quantum dot (QD) as luminescent prob. The ultra-small ZnS QDs were synthesized using a chemical co-precipitation method in the presence of 2-mercaptoethanol (ME) as an efficient capping agent. The prepared pure ZnS QDs was applied as an optical sensor for determination of cyanide ions in aqueous solutions. ZnS nanoparticles have exhibited a strong fluorescent emission at about 424 nm. The fluorescence intensity of QDs is linearly proportional to the cyanide ion concentration in the range 2.44 × 10{sup −6} to 2.59 × 10{sup −5} M with a detection limit of 1.70 × 10{sup −7} M at pH 11. The designed fluorescent sensor possesses remarkable selectivity for cyanide ion over other anions such as Cl{sup −}, Br{sup −}, F{sup −}, I{sup −}, IO{sub 3}{sup −}, ClO{sub 4}{sup −}, BrO{sub 3}{sup −}, CO{sub 3}{sup 2−}, NO{sub 2}{sup −}, NO{sub 3}{sup −}, SO{sub 4}{sup 2−}, S{sub 2}O{sub 4}{sup 2−}, C{sub 2}O{sub 4}{sup 2−}, SCN{sup −}, N{sub 3}{sup −}, citrate and tartarate with negligible influences on the cyanide detection by fluorescence spectroscopy. - Highlights: • Preparation of functionalized ZnS quantum dots in aqueous media • Highly selective quantum dot based luminescent probe for determination of cyanide • Fast and sensitive determination of hazardous CN{sup −} by fluorescence quenching.

  9. A highly selective, colorimetric, and environment-sensitive optical potassium ion sensor.

    Science.gov (United States)

    Song, Guangjie; Sun, Ruofan; Du, Jiqing; Chen, Meiwan; Tian, Yanqing

    2017-05-18

    Potassium ions (K+) play vital roles in many biological processes and thus highly selective sensors for K+ are critical for disease diagnosis and health monitoring. Herein, we report a colorimetric K+ sensor (KS7) in which a hemicyanine dye was used as a fluorophore and phenylaza-[18]crown-6 lariat ether (ACLE) was utilized as a K+ ligand. The maximum absorption peak of KS7 shifted hypsochromically by 77 nm (from 515 to 438 nm) with an isosbestic point at 452 nm upon the addition of K+ to its aqueous solution accompanied by a color change from red to yellow. This sensor exhibited a linear response range to K+ from 1 to 200 mM, indicating its wide detection range for cellular, urinary, and environmental potassium ions. Further, this sensor is solvent-sensitive, implying its environmental sensitivity. For the demonstration of its applications, we prepared filter paper-based K+ test strips, which were used to detect K+ in urine conveniently.

  10. Ion-selective electrodes

    CERN Document Server

    Mikhelson, Konstantin N

    2013-01-01

    Ion-selective electrodes (ISEs) have a wide range of applications in clinical, environmental, food and pharmaceutical analysis as well as further uses in chemistry and life sciences. Based on his profound experience as a researcher in ISEs and a course instructor, the author summarizes current knowledge for advanced teaching and training purposes with a particular focus on ionophore-based ISEs. Coverage includes the basics of measuring with ISEs, essential membrane potential theory and a comprehensive overview of the various classes of ion-selective electrodes. The principles of constructing I

  11. Ion-selective electrode reviews

    CERN Document Server

    Thomas, J D R

    1983-01-01

    Ion-Selective Electrode Reviews, Volume 5 is a collection of articles that covers ion-speciation. The book aims to present the advancements of the range and capabilities of selective ion-sensors. The topics covered in the selection are neutral carrier based ion-selective electrodes; reference electrodes and liquid junction effects in ion-selective electrode potentiometry; ion transfer across water/organic phase boundaries and analytical; and carbon substrate ion-selective electrodes. The text will be of great use to chemists and chemical engineers.

  12. High resolution profiling of ammonium and carbonate with solid contact ion selective electrodes

    Science.gov (United States)

    Athavale, R.; Wehrli, B.; Dinkel, C.; Crespo, G.; Bakker, E.; Brand, A.

    2016-02-01

    Biogeochemical processes involved in the carbon and nitrogen cycle are often confined to very narrow zones in aquatic systems. To study such processes, highly resolved measurements are required, which are not possible by conventional sampling and subsequent laboratory analysis. Potentiometric solid contact ion selective electrodes (SC-ISEs) are promising tools for high resolution in-situ profiling owing to their robustness to pressure changes, their improved detection limits ( 10-6 M) and selectivity and the fast response (t95 ≤ 10s). Conventional SC-ISEs work well under controlled laboratory conditions but can fail to meet the challenges of natural water matrices. In-situ application requires SC-ISEs which are insensitive to changes in redox conditions, pH, and light and to reactive solutes such as high sulfide concentrations. To meet these criteria, we adapted a double layer design by using different combinations of transducing materials and membrane matrices for fabrication of SC-ISEs. We applied these sensors in an custom built profiling set up and demonstrated the potential of this system for high resolution in-situ measurements.

  13. Ion-selective electrode reviews

    CERN Document Server

    Thomas, J D R

    1985-01-01

    Ion-Selective Electrode Reviews, Volume 7 is a collection of papers that covers the applications of electrochemical sensors, along with the versatility of ion-selective electrodes. The coverage of the text includes solid contact in membrane ion-selective electrodes; immobilized enzyme probes for determining inhibitors; potentiometric titrations based on ion-pair formation; and application of ion-selective electrodes in soil science, kinetics, and kinetic analysis. The text will be of great use to chemists and chemical engineers.

  14. Highly selective fluorescent probe for the detection of tin (IV) Ion

    Energy Technology Data Exchange (ETDEWEB)

    Zhu, Leiming; Yang, Jing; Wang, Qiusheng, E-mail: wangqsh@tjut.edu.cn; Zeng, Lintao, E-mail: zlt1981@126.com

    2014-04-15

    A novel fluorescent compound, 7-diethylamino-3-(2'-(1H-imidazo[4,5-b]phenazine)yl)coumarin (DIPC), was synthesized and employed as a fluorescent probe for detecting tin (IV) ion. Upon addition of tin (IV) ion to the solution of DIPC in DMSO–water (9:1, v/v), DIPC exhibited a considerable red-shift in its absorption spectrum and a decrease in fluorescence intensity. These changes result from tin (IV) ion binding to carbonyl oxygen of coumarin and nitrogen of imidazole, reflecting an enhanced ICT process from N,N-diethylamino unit to imidazole unit. The tin (IV) ion selective response was clearly observed by the naked eye through color change. We also studied the bioimaging application of DIPC for detecting tin (IV) ion in Hela cells. And a significant decrease of the fluorescence from the intracellular area was observed. -- Highlights: • We synthesized a novel coumarin derivative (DIPC). • DIPC was used to detect tin (IV) ion selectively. • The detection process was studied upon UV–vis and fluorescence spectrum. • We studied the bioimaging application of DIPC for detecting Sn{sup 4+} ion in cells.

  15. Highly selective and sensitive determination of copper ion by two novel optical sensors

    Directory of Open Access Journals (Sweden)

    Mehrorang Ghaedi

    2017-05-01

    Full Text Available New optical sensors for the determination of copper ion by incorporation of 1,1′-(4-nitro-1,2-phenylenebis(azan-1-yl-1-ylidenebis(methan-1-yl-1-lidenedinaphthalen-2-ol(L1, 1,1′-2,2′-(1,2-phenylenebis(ethene-2,1-diyldinaphthalen-2-ol 1(L2, dibutylphthalate (DBP and sodium tetraphenylborate (Na-TPB to the plasticized polyvinyl chloride matrices were prepared. The tendency of both ionophores (L2 and L1 as chromoionophore was significantly enhanced by the addition of DBP to the membrane. The proposed sensors benefit from advantages such as high stability, reproducibility and relatively long lifetime, good selectivity for Cu2+ ion determination over a large number of alkali, alkaline earth, transition and heavy metal ions. At optimum values of membrane compositions and experimental conditions, both sensors’ response was linear over a concentration range of 7.98 × 10−6 to 1.31 × 10−4mol L−1 and 1.99 × 10−6 to 5.12 × 10−5 mol L−1 for L2 and L1, respectively. Sensor detection limit based on the definition that the concentration of the sample leads to a signal equal to the blank signal plus three times of its standard deviation was found to be 3.99 × 10−7 and 5.88 × 10−7 mol L−1 for L2 and L1, respectively. The response time of the optodes (defined as the time required reaching the 90% of the peak signal was found to be 5–8 min for L2 and 20–25 min for L1 based sensor. The proposed optical sensors were applied successfully for the determination of Cu2+ ion content in water samples.

  16. Ion-selective electrode reviews

    CERN Document Server

    Thomas, J D R

    1982-01-01

    Ion-Selective Electrode Reviews, Volume 3, provides a review of articles on ion-selective electrodes (ISEs). The volume begins with an article on methods based on titration procedures for surfactant analysis, which have been developed for discrete batch operation and for continuous AutoAnalyser use. Separate chapters deal with detection limits of ion-selective electrodes; the possibility of using inorganic ion-exchange materials as ion-sensors; and the effect of solvent on potentials of cells with ion-selective electrodes. Also included is a chapter on advances in calibration procedures, the d

  17. Pure zinc sulfide quantum dot as highly selective luminescent probe for determination of hazardous cyanide ion.

    Science.gov (United States)

    Shamsipur, Mojtaba; Rajabi, Hamid Reza

    2014-03-01

    A rapid and simple fluorescence method is presented for selective and sensitive determination of hazardous cyanide ion in aqueous solution based on functionalized zinc sulfide (ZnS) quantum dot (QD) as luminescent prob. The ultra-small ZnS QDs were synthesized using a chemical co-precipitation method in the presence of 2-mercaptoethanol (ME) as an efficient capping agent. The prepared pure ZnS QDs was applied as an optical sensor for determination of cyanide ions in aqueous solutions. ZnS nanoparticles have exhibited a strong fluorescent emission at about 424 nm. The fluorescence intensity of QDs is linearly proportional to the cyanide ion concentration in the range 2.44×10(-6) to 2.59×10(-5)M with a detection limit of 1.70×10(-7)M at pH11. The designed fluorescent sensor possesses remarkable selectivity for cyanide ion over other anions such as Cl(-), Br(-), F(-), I(-), IO3(-), ClO4(-), BrO3(-), CO3(2-), NO2(-), NO3(-), SO4(2-), S2O4(2-), C2O4(2-), SCN(-), N3(-), citrate and tartarate with negligible influences on the cyanide detection by fluorescence spectroscopy. Copyright © 2013 Elsevier B.V. All rights reserved.

  18. Selected List of Low Energy Beam Transport Facilities for Light-Ion, High-Intensity Accelerators

    Energy Technology Data Exchange (ETDEWEB)

    Prost, L. R. [Fermi National Accelerator Laboratory (FNAL), Batavia, IL (United States)

    2016-02-17

    This paper presents a list of Low Energy Beam Transport (LEBT) facilities for light-ion, high-intensity accelerators. It was put together to facilitate comparisons with the PXIE LEBT design choices. A short discussion regarding the importance of the beam perveance in the choice of the transport scheme follows.

  19. Highly selective potentiometric and colorimetric determinations of cobalt (II) ion using thiazole based ligands.

    Science.gov (United States)

    Singhal, Divya; Singh, Ashok Kumar; Upadhyay, Anjali

    2014-12-01

    New PVC-membrane electrodes were prepared by using 2-((thiazol-2-ylimino)methyl)phenol (L1) and 2-((thiazol-2-ylamino)methyl)phenol (L2) and explored as Co(II) selective electrodes. The effect of various plasticizers and anion excluder was studied in detail and improved performance was observed. It was found that the electrode based on L1 shows better response characteristics in comparison to L2. Optimum performance was observed for the membrane electrode having a composition of L1:NaTPB:DBP:PVC≡2:8:78:62 (w/w, mg). The performance of PME based on L1 was compared with that of CGE. The electrodes exhibit Nernstian slope for Co(II) ions with a limit of detection of 6.91×10(-7) mol L(-1) for PME and 7.94×10(-8) mol L(-1) for CGE. The response time for PME and CGE was found to be 15s and 12 s respectively. The potentiometric responses are independent in the pH range 3.0-9.0 for CGE. The CGE could be used for a period of 90 days. The CGE was used as an indicator electrode in potentiometric titration of EDTA with Co(2+) ion. Further the selectivity of the L1 and L2 was also confirmed by the UV-vis and colorimetric studies and found that L1 is more selective for Co(II) ion. Copyright © 2014 Elsevier B.V. All rights reserved.

  20. A Terbium Metal-Organic Framework for Highly Selective and Sensitive Luminescence Sensing of Hg2+Ions in Aqueous Solution.

    Science.gov (United States)

    Xia, Tifeng; Song, Tao; Zhang, Gege; Cui, Yuanjing; Yang, Yu; Wang, Zhiyu; Qian, Guodong

    2016-12-19

    A series of isomorphic lanthanide metal-organic frameworks (MOFs) Ln(TATAB)⋅(DMF) 4 (H 2 O)(MeOH) 0.5 (LnTATAB, Ln=Eu, Tb, Sm, Dy, Gd; H 3 TATAB=4,4',4''-s-triazine-1,3,5-triyltri-p-aminobenzoic acid) have been solvothermally synthesized and structurally characterized. Among these MOFs, TbTATAB exhibits good water stability and a high fluorescence quantum yield. Because mercury ions (Hg 2+ ) have a high affinity to nitrogen atoms, and the space between multiple nitrogen atoms from triazine and imino groups is suitable for interacting with Hg 2+ ions, TbTATAB shows highly selective and sensitive detection of Hg 2+ in aqueous solution with a detection limit of 4.4 nm. Furthermore, it was successfully applied to detect Hg 2+ ions in natural water samples. © 2016 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  1. Highly selective and quantitative colorimetric detection of mercury(II) ions by carrageenan-functionalized Ag/AgCl nanoparticles.

    Science.gov (United States)

    Narayanan, Kannan Badri; Han, Sung Soo

    2017-03-15

    The natural algal polysaccharide carrageenan was used for the greener synthesis of silver/silver chloride nanoparticles (Carr-Ag/AgCl NPs) without any toxic chemicals. We report the robust, highly selective, and sensitive colorimetric sensing of Hg2+ ions using Carr-Ag/AgCl NPs without any further surface modification. The dark-brown color of a solution of Carr-Ag/AgCl NPs turned to white in a concentration-dependent manner with the addition of Hg2+ ions, confirming the interaction of Carr-Ag/AgCl NPs with Hg2+ ions. The plot of the extinction ratio of absorbance at 350nm to 450nm (A350/A450) for Carr-Ag/AgCl NPs against the concentration of [Hg2+] ions was linear, and the calibration curve was A350/A450=1.05254+0.00318×CHg with a lower detection limit of 1μM. This portable and cost-effective method for mercury(II) ion sensing is widely applicable in on-field qualitative and quantitative measurements of [Hg2+] ions in environmental or biological samples. Copyright © 2016. Published by Elsevier Ltd.

  2. Structural basis for ion selectivity revealed by high-resolution crystal structure of Mg2+ channel MgtE.

    Science.gov (United States)

    Takeda, Hironori; Hattori, Motoyuki; Nishizawa, Tomohiro; Yamashita, Keitaro; Shah, Syed T A; Caffrey, Martin; Maturana, Andrés D; Ishitani, Ryuichiro; Nureki, Osamu

    2014-11-04

    Magnesium is the most abundant divalent cation in living cells and is crucial to several biological processes. MgtE is a Mg(2+) channel distributed in all domains of life that contributes to the maintenance of cellular Mg(2+) homeostasis. Here we report the high-resolution crystal structures of the transmembrane domain of MgtE, bound to Mg(2+), Mn(2+) and Ca(2+). The high-resolution Mg(2+)-bound crystal structure clearly visualized the hydrated Mg(2+) ion within its selectivity filter. Based on those structures and biochemical analyses, we propose a cation selectivity mechanism for MgtE in which the geometry of the hydration shell of the fully hydrated Mg(2+) ion is recognized by the side-chain carboxylate groups in the selectivity filter. This is in contrast to the K(+)-selective filter of KcsA, which recognizes a dehydrated K(+) ion. Our results further revealed a cation-binding site on the periplasmic side, which regulate channel opening and prevents conduction of near-cognate cations.

  3. High-temperature potentiometry: modulated response of ion-selective electrodes during heat pulses.

    Science.gov (United States)

    Chumbimuni-Torres, Karin Y; Thammakhet, Chongdee; Galik, Michal; Calvo-Marzal, Percy; Wu, Jie; Bakker, Eric; Flechsig, Gerd-Uwe; Wang, Joseph

    2009-12-15

    The concept of locally heated polymeric membrane potentiometric sensors is introduced here for the first time. This is accomplished in an all solid state sensor configuration, utilizing poly(3-octylthiophene) as the intermediate layer between the ion-selective membrane and underlying substrate that integrates the heating circuitry. Temperature pulse potentiometry (TPP) gives convenient peak-shaped analytical signals and affords an additional dimension with these sensors. Numerous advances are envisioned that will benefit the field. The heating step is shown to give an increase in the slope of the copper-selective electrode from 31 to 43 mV per 10-fold activity change, with a reproducibility of the heated potential pulses of 1% at 10 microM copper levels and a potential drift of 0.2 mV/h. Importantly, the magnitude of the potential pulse upon heating the electrode changes as a function of the copper activity, suggesting an attractive way for differential measurement of these devices. The heat pulse is also shown to decrease the detection limit by half an order of magnitude.

  4. High Temperature Potentiometry: Modulated Response of Ion-Selective Electrodes During Heat Pulses

    Science.gov (United States)

    Chumbimuni-Torres, Karin Y.; Thammakhet, Chongdee; Galik, Michal; Calvo-Marzal, Percy; Wu, Jie; Bakker, Eric; Flechsig, Gerd-Uwe; Wang, Joseph

    2009-01-01

    The concept of locally heated polymeric membrane potentiometric sensors is introduced here for the first time. This is accomplished in an all solid state sensor configuration, utilizing poly(3-octylthiophene) as intermediate layer between the ion-selective membrane and underlying substrate that integrates the heating circuitry. Temperature pulse potentiometry (TPP) gives convenient peak-shaped analytical signals and affords an additional dimension with these sensors. Numerous advances are envisioned that will benefit the field. The heating step is shown to give an increase in the slope of the copper-selective electrode from 31 mV to 43 mV per 10-fold activity change, with a reproducibility of the heated potential pulses of 1% at 10 µM copper levels and a potential drift of 0.2 mV/h. Importantly, the magnitude of the potential pulse upon heating the electrode changes as a function of the copper activity, suggesting an attractive way for differential measurement of these devices. The heat pulse is also shown to decrease the detection limit by half an order of magnitude. PMID:19928777

  5. Ion-selective organic electrochemical transistors.

    Science.gov (United States)

    Sessolo, Michele; Rivnay, Jonathan; Bandiello, Enrico; Malliaras, George G; Bolink, Henk J

    2014-07-23

    Ion-selective organic electrochemical transistors with sensitivity to potassium approaching 50 μA dec(-1) are demonstrated. The remarkable sensitivity arises from the use of high transconductance devices, where the conducting polymer is in direct contact with a reference gel electrolyte and integrated with an ion-selective membrane. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  6. Monolithic scaffolds for highly selective ion sensing/removal of Co(II), Cu(II), and Cd(II) ions in water.

    Science.gov (United States)

    Shenashen, Mohamed A; El-Safty, Sherif A; Elshehy, Emad A

    2014-12-21

    High exposure to metals, such as cobalt (Co), copper (Cu) and cadmium (Cd), potentially has adverse effects, and can cause severe health problems, leading to a number of specific diseases. This study primarily aims to monitor, detect, separate, and remove the trace concentrations of Co(II), Cu(II), and Cd(II) ions in water, without a preconcentration process, using aluminosilica optical sensor (ASOS) monoliths. These monolithic scaffolds with advantageous physical features (i.e., large surface area-to-volume ratios of the scaffolds, active acid sites and uniform mesocage cubic pores) can strongly induce H-bonding and dispersive interactions with organic chelating agent, resulting in the formation of stable ASOS. In this engineering process, ASOS offers a simple and one-step sensing/capture procedure for the quantification and visual detection of the target elements from water, without requiring sophisticated instrumentation. The key result in this study is the ion selectivity exhibited by the designed ASOS toward the targets, Co(II), Cu(II), and Cd(II) ions, in environmental and waste disposal samples, as well as its reproducibility over a number of analysis/regeneration cycles. These findings can be useful in the fabrication of ASOS can be tailored to suit various applications.

  7. Highly selective detection of phosphate ion based on a single-layered graphene quantum dots-Al3+ strategy.

    Science.gov (United States)

    Chen, Bin Bin; Sheng Li, Rong; Li Liu, Meng; Yan Zou, Hong; Liu, Hui; Huang, Cheng Zhi

    2018-02-01

    Determination of phosphate ion (PO43-) is important in biomedical and environmental arrays because its controlling concentrations are associated with different pathologies or the quality of water. Herein, we report a new type of photoluminescence (PL) probe for highly selective detection of PO43- based on a single-layered graphene quantum dots chelating with aluminium ions (s-GQDs-Al3+) system. The PL of s-GQDs can be enhanced by Al3+ through the aggregation-induced emission enhancement (AIEE) effect. With the addition of PO43-, the PL of the s-GQDs-Al3+ system is faded away because PO43- has stronger coordination with Al3+ which results in the elimination of AIEE effect and the decrease in the PL intensity of the s-GQDs-Al3+ system. Therefore, the s-GQDs-Al3+ system can behave as an on-off type PL probe for PO43- detection. It is found that the PL intensity ratio (I/I0) of s-GQDs in the presence of Al3+ at 463nm is proportional to the concentration of PO43- in the range of 0.25-7.5μM with the limit of detection as low as 0.1μM. This selective assay has a great application prospect in the complex matrixes owing to its simplicity and specificity for PO43- detection. Copyright © 2017 Elsevier B.V. All rights reserved.

  8. Highly selective and sensitive determination of copper ion by two novel optical sensors

    OpenAIRE

    Ghaedi, Mehrorang; Tashkhourian, Javad; Montazerozohori, Morteza; Nejati Biyareh, Mahdi; Sadeghian, Batool

    2013-01-01

    New optical sensors for the determination of copper ion by incorporation of 1,1′-(4-nitro-1,2-phenylene)bis(azan-1-yl-1-ylidene)bis(methan-1-yl-1-lidene)dinaphthalen-2-ol(L1), 1,1′-2,2′-(1,2-phenylene)bis(ethene-2,1-diyl)dinaphthalen-2-ol 1(L2), dibutylphthalate (DBP) and sodium tetraphenylborate (Na-TPB) to the plasticized polyvinyl chloride matrices were prepared. The tendency of both ionophores (L2 and L1) as chromoionophore was significantly enhanced by the addition of DBP to the membrane...

  9. TOPICAL REVIEW: Highly charged ions

    Science.gov (United States)

    Gillaspy, J. D.

    2001-10-01

    This paper reviews some of the fundamental properties of highly charged ions, the methods of producing them (with particular emphasis on table-top devices), and their use as a tool for both basic science and applied technology. Topics discussed include: charge dependence and scaling laws along isoelectronic or isonuclear sequences (for wavefunction size or Bohr radius, ionization energy, dipole transition energy, relativistic fine structure, hyperfine structure, Zeeman effect, Stark effect, line intensities, linewidths, strength of parity violation, etc), changes in angular momentum coupling schemes, selection rules, interactions with surfaces, electron-impact ionization, the electron beam ion trap (EBIT), ion accelerators, atomic reference data, cosmic chronometers, laboratory x-ray astrophysics, vacuum polarization, solar flares, ion implantation, ion lithography, ion microprobes (SIMS and x-ray microscope), nuclear fusion diagnostics, nanotechnology, quantum computing, cancer therapy and biotechnology.

  10. 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

  11. Functionality Selection Principle for High Voltage Lithium-ion Battery Electrolyte Additives

    Energy Technology Data Exchange (ETDEWEB)

    Su, Chi-Cheung; He, Meinan [Department; Peebles, Cameron; Zeng, Li; Tornheim, Adam; Liao, Chen; Zhang, Lu; Wang, Jie; Wang, Yan [Department; Zhang, Zhengcheng

    2017-08-30

    A new class of electrolyte additives based on cyclic fluorinated phosphate esters was rationally designed and identified as being able to stabilize the surface of a LiNi0.5Mn0.3Co0.2O2 (NMC532) cathode when cycled at potentials higher than 4.6 V vs Li+/Li. Cyclic fluorinated phosphates were designed to incorporate functionalities of various existing additives to maximize their utilization. The synthesis and characterization of these new additives are described and their electrochemical performance in a NMC532/graphite cell cycled between 4.6 and 3.0 V are investigated. With 1.0 wt % 2-(2,2,2-trifluoroethoxy)-1,3,2-dioxaphospholane 2-oxide (TFEOP) in the conventional electrolyte the NMC532/graphite cell exhibited much improved capacity retention compared to that without any additive. The additive is believed to form a passivation layer on the surface of the cathode via a sacrificial polymerization reaction as evidenced by X-ray photoelectron spectroscopy (XPS) and nuclear magnetic resonsance (NMR) analysis results. The rational pathway of a cathode-electrolyte-interface formation was proposed for this type of additive. Both experimental results and the mechanism hypothesis suggest the effectiveness of the additive stems from both the polymerizable cyclic ring and the electron-withdrawing fluorinated alkyl group in the phosphate molecular structure. The successful development of cyclic fluorinated phosphate additives demonstrated that this new functionality selection principle, by incorporating useful functionalities of various additives into one molecule, is an effective approach for the development of new additives.

  12. A robust microporous metal-organic framework as a highly selective and sensitive, instantaneous and colorimetric sensor for Eu³⁺ ions.

    Science.gov (United States)

    Gao, Yanfei; Zhang, Xueqiong; Sun, Wei; Liu, Zhiliang

    2015-01-28

    An extremely thermostable magnesium metal-organic framework (Mg-MOF) is reported for use as a highly selective and sensitive, instantaneous and colorimetric sensor for Eu(3+) ions. There has been extensive interest in the recognition and sensing of ions because of their important roles in biological and environmental systems. However, only a few of these systems have been explored for specific rare earth ion detection. A robust microporous Mg-MOF for the recognition and sensing of Eu(3+) ions with high selectivity at low concentrations in aqueous solutions has been synthesized. This stable metal-organic framework (MOF) contains nanoscale holes and non-coordinating nitrogen atoms inside the walls of the holes, which makes it a potential host for foreign metal ions. Based on the energy level matching and efficient energy transfer between the host and the guest, the Mg-MOF sensor is both highly selective and sensitive as well as instantaneous; thus, it is a promising approach for the development of luminescent probing materials with unprecedented applications and its use as an Eu(3+) ion sensor.

  13. Criteria for selection of target materials and design of high-efficiency-release targets for radioactive ion beam generation

    CERN Document Server

    Alton, G D; Liu, Y

    1999-01-01

    In this report, we define criteria for choosing target materials and for designing, mechanically stable, short-diffusion-length, highly permeable targets for generation of high-intensity radioactive ion beams (RIBs) for use at nuclear physics and astrophysics research facilities based on the ISOL principle. In addition, lists of refractory target materials are provided and examples are given of a number of successful targets, based on these criteria, that have been fabricated and tested for use at the Holifield Radioactive Ion Beam Facility (HRIBF).

  14. Highly selective colorimetric detection and preconcentration of Bi(III) ions by dithizone complexes anchored onto mesoporous TiO2

    Science.gov (United States)

    Faisal, Mohd; Ismail, Adel A.; Harraz, Farid A.; Bouzid, Houcine; Al-Sayari, Saleh A.; Al-Hajry, Ali

    2014-02-01

    We successfully developed a single-step detection and removal unit for Bi(III) ions based on dithizone (DZ) anchored on mesoporous TiO2 with rapid colorometric response and high selectivity for the first time. [(DZ)3-Bi] complex is easily separated and collected by mesoporous TiO2 as adsorbent and preconcentrator without any color change of the produced complex onto the surface of mesoporous TiO2 (TiO2-[(DZ)3-Bi]) at different Bi(III) concentrations. This is because highly potent mesoporous TiO2 architecture provides proficient channeling or movement of Bi(III) ions for efficient binding of metal ion, and the simultaneous excellent adsorbing nature of mesoporous TiO2 provides an extra plane for the removal of metal ions.

  15. Highly Selective Detection of Silver in the Low ppt Range with Ion-Selective Electrodes Based on Ionophore-Doped Fluorous Membranes

    Science.gov (United States)

    Lai, Chun-Ze; Fierke, Melissa A.; Costa, Rosenildo Corrêa da; Gladysz, John A.; Stein, Andreas; Bühlmann, Philippe

    2010-01-01

    Ionophore-doped sensing membranes exhibit greater selectivities and wider measuring ranges if their membrane matrixes are noncoordinating and solvate interfering ions poorly. This is particularly true for fluorous phases, which are the least polar and polarizable condensed phases known. In this work, fluorous membrane matrixes were used to prepare silver ion-selective electrodes (ISEs). Sensing membranes composed of perfluoroperhydrophenanthrene, sodium tetrakis[3,5-bis(perfluorohexyl)phenyl]borate, and one of four fluorophilic Ag+-selective ionophores with one or two thioether groups were investigated. All electrodes exhibited Nernstian responses to Ag+ in a wide range of concentrations. Their selectivities for Ag+ over interfering ions were found to depend on host preorganization and the length of the –(CH2)n– spacers separating the coordinating thioether group from the strongly electron withdrawing perfluoroalkyl groups. ISEs based on the most selective of the four ionophores, i.e., 1,3-bis(perfluorodecylethylthiomethyl)benzene, provided much higher selectivities for Ag+ over many alkaline and heavy metal ions than most Ag+ ISEs reported in the literature (e.g., logKAg,Jpot for K+, −11.6; Pb2+, −10.2; Cu2+, −13.0; Cd2+, −13.2). Moreover, the use of this ionophore with a linear perfluorooligoether as membrane matrix and solid contacts consisting of three-dimensionally ordered macroporous (3DOM) carbon resulted in a detection limit for Ag+ of 4.1 ppt (3.8×10−11 M). PMID:20799720

  16. Construction of three lanthanide metal-organic frameworks: Synthesis, structure, magnetic properties and highly selective sensing of metal ions

    Science.gov (United States)

    Zhang, Xiu-Mei; Li, Peng; Gao, Wei; Liu, Feng; Liu, Jie-Ping

    2016-12-01

    Three lanthanide metal-organic frameworks (Ln-MOFs), [Ln(TZI)(H2O)4]·3H2O (Ln=Gd (1) and Tb (2) and Dy (3), H3TZI=5-(1H-tetrazol-5-yl)isophthalic acid), have been synthesized under hydrothermal conditions. Single crystal X-ray diffraction reveals that 1-3 are isostructural and display a 1D double chain based on dinuclear motifs with (μ-COO)2 double bridges. Magnetic studies indicate antiferromagnetic interactions in 1, ferromagnetic interactions in 2 and 3. Furthermore, compound 3 displays a slow relaxation behavior. Compound 2 exhibits intense characteristic green emission of Tb(III) ions in the solid state, which can be observed by the naked eye under UV light. Interestingly, 2 can selectively sense Pb2+ and Fe3+ ions through luminescence enhancement and quenching, respectively. The luminescence quenching mechanisms have been investigated in detail. The study on luminescence Ln-MOFs as a probe for sensing Pb2+ and Fe3+ ions is exceedingly rare example.

  17. Highly Selective and Sensitive Detection of Cu(2+) Ions Using Ce(III)/Tb(III)-Doped SrF2 Nanocrystals as Fluorescent Probe.

    Science.gov (United States)

    Sarkar, Shyam; Chatti, Manjunath; Adusumalli, Venkata N K B; Mahalingam, Venkataramanan

    2015-11-25

    We report a green synthetic approach to the synthesis of water dispersible Ce(3+)/Tb(3+)-doped SrF2 nanocrystals, carried out using environment friendly microwave irradiation with water as solvent. The nanocrystals display strong green emission due to energy transfer from Ce(3+) to Tb(3+) ions. This strong green emission from Tb(3+) ions is selectively quenched upon addition of Cu(2+) ions, thus making the nanocrystals a potential Cu(2+) ions sensing material. There is barely any interference by other metal ions on the detection of Cu(2+) ions and the detection limit is as low as 2 nM. This sensing ability is highly reversible by the addition of ethylenediaminetetraacetic acid (EDTA) with the recovery of almost 90% of the original luminescence. The luminescence quenching and recovery cycle was repeated multiple times without much effect on the sensitivity. The study was extended to real world water samples and obtained similar results. In addition to the sensing, we strongly predict the small size and high luminescence of the Ce(3+)/Tb(3+)-doped SrF2 nanocrystals can be used for bioimaging applications.

  18. High-resolution radial distribution function of pure ion-implanted amorphous silicon measured using tilted-illumination selected-area electron diffraction.

    Science.gov (United States)

    Gorecki, Alexander; Liu, Amelia C Y; Petersen, Timothy C

    2014-02-01

    High-resolution radial distribution functions of as-implanted and thermally relaxed amorphous silicon created by ion implantation were measured using tilted-illumination selected area electron diffraction at room temperature. The diffracted intensities were measured out to a maximum scattering vector 2 sin(θ)/λ of 3.3-3.7 Å-1. The volume-averaged pair-correlation statistics of as-implanted and relaxed ion-implanted amorphous silicon are virtually indistinguishable with coordination numbers of 3.7 ± 0.3 and 3.9 ± 0.3 (for neighbors closer than 3 Å) and average bond angles of 109 ± 0.5° and 110 ± 0.6°, respectively. The atomic rearrangements in ion-implanted amorphous silicon due to a low temperature anneal are subtle.

  19. Microspheres aided introduction of ionophore and ion-exchanger to the ion-selective membrane.

    Science.gov (United States)

    Wojciechowski, Marcin; Kisiel, Anna; Bulska, Ewa; Michalska, Agata

    2012-01-15

    In this work a novel method for introduction of ionophore and ion-exchanger to the ion-selective polyacrylate based membrane is proposed. These compounds (and optionally primary ions) are introduced to polyacrylate microspheres, used to prepare ion-selective membrane. The approach proposed here can be used to prepare membranes containing primary ions equally distributed through the receptor phase, i.e. membranes that do not require conditioning in primary ions solution and are free from problems related to slow diffusion of primary ions. Thus obtained sensors were characterized with linear responses (also at relatively high activities) and high selectivities, despite considerable reduction of ionophore and ion-exchanger amount introduced to the membrane. To be able to prepare ion-selective membranes using this approach, a method for quantification of ionophore and ion-exchanger introduced into microspheres is required. In this work a novel method utilizing high performance liquid chromatography (HPLC) with DAD or FLD detection is proposed. Incorporation of ionophore and ion-exchanger into the microspheres was achieved either by absorption into ready spheres or in course of photopolymerization of polymeric beads. The obtained results have proven that both procedures led to incorporation of ionophore/ion-exchanger into polymeric spheres, however, the content of the compounds in the spheres post process is different from their ratio in solution from which they had been introduced. These effects need to be considered/compensated while preparing microspheres containing ion-selective membranes. As a model system poly(n-butyl acrylate) spheres, silver selective ionophore and sodium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate were chosen, resulting ultimately in silver-selective electrodes. Copyright © 2011 Elsevier B.V. All rights reserved.

  20. Eu(III)-functionalized MIL-124 as fluorescent probe for highly selectively sensing ions and organic small molecules especially for Fe(III) and Fe(II).

    Science.gov (United States)

    Xu, Xiao-Yu; Yan, Bing

    2015-01-14

    A layerlike MOF (MIL-124, orGa2(OH)4(C9O6H4)) has been prepared and chosen as a parent compound to encapsulate Eu(3+) cations by one uncoordinated carbonyl group in its pores. The Eu(3+)-incorporated sample (Eu(3+)@MIL-124) is fully characterized, which shows excellent luminescence and good fluorescence stability in water or other organic solvents. Subsequently, we choose Eu(3+)@MIL-124 as sensitive probe for sensing metal ions, anions, and organic small molecules because of its robust framework. Studying of the luminescence properties reveals that the complex Eu(3+)@MIL-124 was developed as a highly selective and sensitive probe for detection of Fe(3+) (detection limit, 0.28 μM) and Fe(2+) ions through fluorescence quenching of Eu(3+) and MOF over other metal ions. In connection to this, a probable sensing mechanism was also discussed in this paper. In addition, when Eu(3+)@MIL-124 was immersed in the different anions solutions and organic solvents, it also shows highly selective for Cr2O7(2-)(detection limit, 0.15 μM)and acetone. Remarkably, it is the first Eu-doped MOF to exhibit an excellent ability for the detection of Fe(3+) and Fe(2+) in an aqueous environment without any structural disintegration of the framework.

  1. Atomic Oxygen (ATOX) simulation of Teflon FEP and Kapton H surfaces using a high intensity, low energy, mass selected, ion beam facility

    Science.gov (United States)

    Vered, R.; Grossman, E.; Lempert, G. D.; Lifshitz, Y.

    1994-01-01

    A high intensity (greater than 10(exp 15) ions/sq cm) low energy (down to 5 eV) mass selected ion beam (MSIB) facility was used to study the effects of ATOX on two polymers commonly used for space applications (Kapton H and Teflon FEP). The polymers were exposed to O(+) and Ne(+) fluences on 10(exp 15) - 10(exp 19) ions/sq cm, using 30eV ions. A variety of analytical methods were used to analyze the eroded surfaces including: (1) atomic force microscopy (AFM) for morphology measurements; (2) total mass loss measurements using a microbalance; (3) surface chemical composition using x-ray photoelectron spectroscopy (XPS), and (4) residual gas analysis (RGA) of the released gases during bombardment. The relative significance of the collisional and chemical degradation processes was evaluated by comparing the effects of Ne(+) and O(+) bombardment. For 30 eV ions it was found that the Kapton is eroded via chemical mechanisms while Teflon FEP is eroded via collisional mechanisms. AFM analysis was found very powerful in revealing the evolution of the damage from its initial atomic scale (roughness of approx. 1 nm) to its final microscopic scale (roughness greater than 1 micron). Both the surface morphology and the average roughness of the bombarded surfaces (averaged over 1 micron x 1 micron images by the system's computer) were determined for each sample. For 30 eV a non linear increase of the Kapton roughness with the O(+) fluence was discovered (a slow increase rate for fluences phi less than 5 x 10(exp 17) O(+)/sq cm, and a rapid increase rate for phi greater than 5 x 10(exp 17) O(+)/sq cm). Comparative studies on the same materials exposed to RF and DC oxygen plasmas indicate that the specific details of the erosion depend on the simulation facility emphasizing the advantages of the ion beam facility.

  2. Mechanisms of valence selectivity in biological ion channels.

    Science.gov (United States)

    Corry, B; Chung, S-H

    2006-02-01

    Transmembrane ion channels play a crucial role in the existence of all living organisms. They partition the exterior from the interior of the cell, maintain the proper ionic gradient across the cell membrane and facilitate signaling between cells. To perform these functions, ion channels must be highly selective, allowing some types of ions to pass while blocking the passage of others. Here we review a number of studies that have helped to elucidate the mechanisms by which ion channels discriminate between ions of differing charge, focusing on four channel families as examples: gramicidin, ClC chloride, voltage-gated calcium and potassium channels. The recent availability of high-resolution structural data has meant that the specific inter-atomic interactions responsible for valence selectivity can be pinpointed. Not surprisingly, electrostatic considerations have been shown to play an important role in ion specificity, although many details of the origins of this discrimination remain to be determined.

  3. Fluorescent Aromatic Tag-Functionalized MOFs for Highly Selective Sensing of Metal Ions and Small Organic Molecules.

    Science.gov (United States)

    Zhao, Si-Si; Yang, Jin; Liu, Ying-Ying; Ma, Jian-Fang

    2016-03-07

    By varying the fluorescent tags of resorcin[4]arene-based tetracarboxylic acids from phenyl to naphthyl, two highly luminescent metal-organic frameworks (MOFs), namely, [Zn2(TPC4A)(DMF)(H2O)4]·3H2O (1) and [(CH3)2NH2]2[Zn(TNC4A)]·4H2O (2), were successfully achieved (TPC4A = 2,8,14,20-tetra-phenyl-6,12,18,24-tetra-methoxy-4,10,16,22-tetra-carboxy-methoxy-resorcin[4]arene and TNC4A = 2,8,14,20-tetra-1-naphthal-6,12,18,24-tetra- methoxy-4,10,16,22-tetra-carboxy-methoxy-resorcin[4]arene). Compound 1 features a unique 2D network, while 2 exhibits a fascinating 3D framework. The highly selective detection of small organic molecules as well as Fe(2+) and Fe(3+) was performed for 1 and 2 as fluorescent sensors. Remarkably, luminescent 1 and 2 were used as sensory materials for the sensing of various amine vapors with high selectivity and rapid response. Most strikingly, clear fluorescence "on-off" switch-functions toward small organic molecules as well as amine vapors were also explored for luminescent 1 and 2.

  4. Impact of Selected LiPF6 Hydrolysis Products on the High Voltage Stability of Lithium-Ion Battery Cells.

    Science.gov (United States)

    Wagner, Ralf; Korth, Martin; Streipert, Benjamin; Kasnatscheew, Johannes; Gallus, Dennis R; Brox, Sebastian; Amereller, Marius; Cekic-Laskovic, Isidora; Winter, Martin

    2016-11-16

    Diverse LiPF6 hydrolysis products evolve during lithium-ion battery cell operation at elevated operation temperatures and high operation voltages. However, their impact on the formation and stability of the electrode/electrolyte interfaces is not yet investigated and understood. In this work, literature-known hydrolysis products of LiPF6 dimethyl fluorophosphate (DMFP) and diethyl fluorophosphate (DEFP) were synthesized and characterized. The use of DMFP and DEFP as electrolyte additive in 1 M LiPF6 in EC:EMC (1:1, by wt) was investigated in LiNi1/3Mn1/3Co1/3O2/Li half cells. When charged to a cutoff potential of 4.6 V vs Li/Li+, the additive containing cells showed improved cycling stability, increased Coulombic efficiencies, and prolonged shelf life. Furthermore, low amounts (1 wt % in this study) of the aforementioned additives did not show any negative effect on the cycling stability of graphite/Li half cells. DMFP and DEFP are susceptible to oxidation and contribute to the formation of an effective cathode/electrolyte interphase as confirmed by means of electrochemical stability window determination, and X-ray photoelectron spectroscopy characterization of pristine and cycled electrodes, and they are supported by computational calculations.

  5. Magic sized ZnS quantum dots as a highly sensitive and selective fluorescence sensor probe for Ag+ ions.

    Science.gov (United States)

    Mandal, Abhijit; Dandapat, Anirban; De, Goutam

    2012-02-07

    A green and simple chemical synthesis of magic sized water soluble blue-emitting ZnS quantum dots (QDs) has been accomplished by reacting anhydrous Zn acetate, sodium sulfide and thiolactic acid (TLA) at room temperature in aqueous solution. Refluxing of this mixture in open air yielded ZnS clusters of about 3.5 nm in diameter showing very strong and narrow photoluminescence properties with long stability. Refluxing did not cause any noticeable size increment of the clusters. As a result, the QDs obtained after different refluxing conditions showed similar absorption and photoluminescence (PL) features. Use of TLA as a capping agent effectively yielded such stable and magic sized QDs. The as-synthesized and 0.5 h refluxed ZnS QDs were used as a fluorescence sensor for Ag(+) ions. It has been observed that after addition of Ag(+) ions of concentration 0.5-1 μM the strong fluorescence of ZnS QDs was almost quenched. The quenched fluorescence can be recovered by adding ethylenediamine to form a complex with Ag(+) ions. The other metal ions (K(+), Ca(2+), Au(3+), Cu(2+), Fe(3+), Mn(2+), Mg(2+), Co(2+)) showed little or no effect on the fluorescence of ZnS QDs when tested individually or as a mixture. In the presence of all these ions, Ag(+) responded well and therefore ZnS QDs reported in this work can be used as a Ag(+) ion fluorescence sensor.

  6. A polyamide receptor based benzothiazole derivative: highly selective and sensitive fluorescent sensor for Hg{sup 2+} ion in aqueous medium

    Energy Technology Data Exchange (ETDEWEB)

    Maity, Shubhra Bikash; Bharadwaj, Parimal K., E-mail: pkb@iitk.ac.in

    2015-05-15

    A water soluble benzothiazole derivative having polyamide arms has been designed and synthesized. The sensor selectively detects Hg{sup 2+} ion in aqueous medium in presence of alkali, alkaline earth, first row transition metal and heavy metal ions. The reversible behaviour of the sensor can be achieved in presence of iodide ion. - Highlights: • A benzothiazole derivative having polyamide arms has been designed and synthesized. • It selectively detects Hg{sup 2+} ion in presence of host of monovalent, divalent and trivalent ions in aqueous medium. • It works through a reversible way. • The detection limit for Hg{sup 2+} ion was found to be 7.15×10{sup −7} M.

  7. Highly selective and sensitive optical sensor for determination of Pb2+and Hg2+ ions based on the covalent immobilization of dithizone on agarose membrane

    Science.gov (United States)

    Zargoosh, Kiomars; Babadi, Fatemeh Farhadian

    2015-02-01

    A highly sensitive and selective optical membrane for determination of Hg2+ and Pb2+ was prepared by covalent immobilization of dithizone on agarose membrane. In addition to its high stability, reproducibility and relatively long lifetime, the proposed optical sensor revealed good selectivity for target ions over a large number of alkali, alkaline earth, transition, and heavy metal ions. The proposed optical membrane displays linear responses from 1.1 × 10-8 to 2.0 × 10-6 mol L-1 and 1.2 × 10-8 to 2.4 × 10-6 mol L-1 for Hg2+ and Pb2+, respectively. The limits of detection (LOD) were 2.0 × 10-9 mol L-1 and 4.0 × 10-9 mol L-1 for Hg2+ and Pb2, respectively. The prepared optical membrane was successfully applied to the determination of Hg2+ and Pb2+ in industrial wastes, spiked tap water and natural waters without any preconcentration step.

  8. Ion selective electrodes based on chalcogenide glasses

    OpenAIRE

    Conde Garrido, Juan Manuel; Ureña, Maria Andrea; Arcondo, Bibiana Graciela

    2017-01-01

    The properties of chalcogenide glasses as sensitive membranes in ion selective electrodes (ISEs) have been investigated. It is shown that ISEs based on the AgGeSe system show sensitivity to the presence of Ag+ and Cu2+ ions in aqueous solutions and in both cases they exhibit super-nernstian responses. The analytical properties such as reproducibility, linear range, sensitivity and detection limit were studied. The response of the electrodes is apparently conditioned by the amount of Ag in the...

  9. Colloidal GdVO4:Eu3+@SiO2 nanocrystals for highly selective and sensitive detection of Cu2+ ions

    Science.gov (United States)

    Liang, Yanjie; Noh, Hyeon Mi; Park, Sung Heum; Choi, Byung Chun; Jeong, Jung Hyun

    2018-03-01

    Nowadays, in view of health and safety demands, the controlled design of selective and sensitive sensors for Cu2+ detection is of considerable importance. Therefore, we construct herein core-shell colloidal GdVO4:Eu3+@SiO2 nanocrystals (NCs) as optical sensor for the detection of Cu2+, which were synthesized by a facile hydrothermal reaction and encapsulated with a uniform layer of ultrathin silica through a sol-gel strategy. The NCs present strong red emission due to energy transfer from VO43- groups to Eu3+ when exciting with ultraviolet (UV) light. This intense red emission from Eu3+ could be selectively quenched in the presence of Cu2+ in comparison to other metal ions and the limit of detection is as low as 80 nM in aqueous solution. It is revealed that the spectral overlap between the emission band of NCs and the absorption of Cu2+ accounts for this intriguing luminescence behavior. The detection ability is highly reversible by the addition of ethylenediaminetetraacetic acid (EDTA) with the recovery of almost 100% of the original luminescence. The luminescence quenching and recovery processes can be performed repeatedly with good sensing ability. These remarkable performances allow the colloidal GdVO4:Eu3+@SiO2 NCs a promising fluorescence chemosensor for detecting Cu2+ ions in aqueous solution.

  10. Spectroscopy of mobility-selected biomolecular ions.

    Science.gov (United States)

    Papadopoulos, Georgios; Svendsen, Annette; Boyarkin, Oleg V; Rizzo, Thomas R

    2011-01-01

    We describe here experiments that combine differential ion mobility, which separates conformational isomers of biomolecular ions, with electronic spectroscopy in a cold, radio-frequency ion trap. Although the low temperature attainable in a cold ion trap greatly simplifies the electronic spectra of large molecules, conformational heterogeneity can still be a significant source of congestion, complicating spectroscopic analysis. We demonstrate here that using differential ion mobility to separate gas-phase peptide conformers before injecting them into a cold ion trap allows one to decompose a dense spectrum into contributions from different conformational families. In the inverse sense, cold ion spectroscopy can be used as a conformation-specific detector for ion mobility, allowing one to separate an unresolved peak into contributions from different conformational families. The doubly protonated peptide bradykinin serves as a good test case for the marriage of these two techniques as it exhibits a considerable degree of conformational heterogeneity that results in a highly congested electronic spectrum. Our results demonstrate the feasibility and advantages of directly coupling ion mobility with spectroscopy and provide a diagnostic of conformational isomerization of this peptide after being produced in the gas phase by electrospray.

  11. Selective Ion-permeation through Strained and Charged Graphene Membranes.

    Science.gov (United States)

    Li, Kun; Tao, Yi; Li, Zhongwu; Sha, Jingjie; Chen, Yunfei

    2017-11-16

    By means of molecular dynamics (MD) simulations and density functional theory (DFT) calculations, we demonstrate that stretched and charged graphene can act as ion sieve membranes. It is observed that loading 30% strain on graphene can induce pores in the dense electron cloud to allow ions to pass through the aromatic rings. Meanwhile, charged surface is helpful to peel the hydration layers from the ions and decrease the energy barrier for ion translocation through nanopores. Our results suggest that with membrane charge density of 6.80 e/nm2, Li+ can be highly purified from the mixed solution including Li+, K+, Na+ and Cl- ions. Further increasing the charge density to 15.78 e/nm2 can obtain excellent Na+/K+ selectivity. The potential of mean force (PMF) profiles of ion permeation reveal that the potential for each ion is quite different. Fine tuning membrane charge density, pristine monolayer graphene can act as ion sieves with both high permeability and high selectivity. © 2017 IOP Publishing Ltd.

  12. Selective ion-permeation through strained and charged graphene membranes

    Science.gov (United States)

    Li, Kun; Tao, Yi; Li, Zhongwu; Sha, Jingjie; Chen, Yunfei

    2018-01-01

    By means of molecular dynamics simulations and density functional theory calculations, we demonstrate that stretched and charged graphene can act as ion sieve membranes. It is observed that loading 30% strain on graphene can induce pores in the dense electron cloud to allow ions to pass through the aromatic rings. Meanwhile, a charged surface is helpful to peel the hydration layers from the ions and decrease the energy barrier for ion translocation through nanopores. Our results suggest that with a membrane charge density of 6.80 e nm‑2, Li+ can be highly purified from the mixed solution including Li+, K+, Na+ and Cl‑ ions. Further increasing the charge density to 15.78 e nm‑2 can obtain excellent Na+/K+ selectivity. The potential of mean force profiles of ion permeation reveal that the potential for each ion is quite different. By fine tuning membrane charge density, pristine monolayer graphene can act as ion sieves with both high permeability and high selectivity.

  13. Microfluidic Systems with Ion-Selective Membranes

    Science.gov (United States)

    Slouka, Zdenek; Senapati, Satyajyoti; Chang, Hsueh-Chia

    2014-06-01

    When integrated into microfluidic chips, ion-selective nanoporous polymer and solid-state membranes can be used for on-chip pumping, pH actuation, analyte concentration, molecular separation, reactive mixing, and molecular sensing. They offer numerous functionalities and are hence superior to paper-based devices for point-of-care biochips, with only slightly more investment in fabrication and material costs required. In this review, we first discuss the fundamentals of several nonequilibrium ion current phenomena associated with ion-selective membranes, many of them revealed by studies with fabricated single nanochannels/nanopores. We then focus on how the plethora of phenomena has been applied for transport, separation, concentration, and detection of biomolecules on biochips.

  14. Highly selective "turn-on" fluorescent sensing of fluoride ion based on a conjugated polymer thin film-Fe3+ complex.

    Science.gov (United States)

    Ding, Wanchuan; Xu, Jingkun; Wen, Yangping; Zhang, Jie; Liu, Hongtao; Zhang, Zhouxiang

    2017-05-15

    We designed a new fluorescent conjugated polymer thin film sensor via direct electropolymerization of the corresponding electroactive monomer M onto the surface of ITO electrode, and the thin film-Fe3+ complex was used for the highly-selective detection of fluoride ion (F-) in water environmental samples. The as-obtained thin film could effectively detect Fe3+ as a selective turn-off fluorescent sensor, and exhibited outstanding reversibility. This film in the presence of Fe3+ showed a highly selective turn-on response toward F- over other anions with a 5-fold enhancement in the fluorescence intensity. F- with a relatively wide concentration range from 10 μM to 3 mM could be determined in a rather simple and sensitive manner with a detection limit of 6.78 μM (0.128 ppm). Analytical applicability of the film-Fe3+ complex for determining the levels of F- in environmental water samples has been successfully demonstrated by fluorescent analysis with satisfactory results. This strategy will provide a new approach for the facile design of new molecular sensing devices and practical application in environments. Copyright © 2017 Elsevier B.V. All rights reserved.

  15. Multilayered ion-imprinted membranes with high selectivity towards Li+ based on the synergistic effect of 12-crown-4 and polyether sulfone

    Science.gov (United States)

    Lu, Jian; Qin, Yingying; Zhang, Qi; Wu, Yilin; Cui, Jiuyun; Li, Chunxiang; Wang, Liang; Yan, Yongsheng

    2018-01-01

    High-selective multilayered Li+-imprinted membranes (Li-IIMs) with enhanced hydrophilicity and stability were developed based on polyether sulfone substrate membranes. The multilayered structure was prepared with polydopamine (pDA) as the interfacial adhesion layer, SiO2 nanoparticles as the hydrophilic layer and Li+-imprinted polymers as the imprinted layer. The selective ;Li+-recognition sites; were formed using 12-crown-4 (12C4) as the adsorbing units. The optimal relative selectivity coefficients (α) of Li+/Na+ and Li+/K+ reached up to 1.85 and 2.07 with the imprinting factor (β) of 2.51, and the high permselectivity factors (γ) of Na+/Li+ (7.39) and K+/Li+ (9.86) were achieved on Li-IIMs. The Langmuir isotherm model and the pseudo-second-order kinetics model best fitted the rebinding data of Li-IIMs, as well as the rebinding capacities reached up to 90.3% of initial binding after 5 cycles of adsorption/desorption and just declined to 88.1% after another 5 cycles a month later. Therefore, the as-prepared Li-IIMs would have potential applications for the separation of lithium ions from salt lake brines.

  16. Highly fluorescent carbon dots as selective and visual probes for sensing copper ions in living cells via an electron transfer process.

    Science.gov (United States)

    Wang, Jian; Sheng Li, Rong; Zhi Zhang, Hong; Wang, Ni; Zhang, Zheng; Huang, Cheng Zhi

    2017-11-15

    As an integral part of many important enzymes, Cu2+ is involved in a number of vital biological processes, which is linked to the oxidative damage and environmental contamination when Cu2+ is excessive. In this work, Cu2+ can be captured by the amino groups of carbon dots (CDs) to form complexes, resulting in a strong fluorescence quenching of CDs via a nonradiative electron transfer process, which offered a rapid, visual, and selective methodology for Cu2+ detection. The probe exhibited a wide response concentration range (0.01-2μM) to Cu2+ with a detection limit of 6.7nM. Significantly, the CDs presented excellent biocompatibility and high photostability, which were applicable for the visualization of Cu2+ dynamic invasion into living cells and Tilapia mossambica. Furthermore, the toxicity of Cu2+ ions to living cells could be inhibited with CDs by the formation of complexes. Copyright © 2017. Published by Elsevier B.V.

  17. 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.

  18. Hydrophilic Nb{sup 5+}-immobilized magnetic core–shell microsphere – A novel immobilized metal ion affinity chromatography material for highly selective enrichment of phosphopeptides

    Energy Technology Data Exchange (ETDEWEB)

    Sun, Xueni; Liu, Xiaodan; Feng, Jianan [Pharmaceutical Analysis Department, School of Pharmacy, Fudan University, Shanghai 201203 (China); Li, Yan, E-mail: yanli@fudan.edu.cn [Pharmaceutical Analysis Department, School of Pharmacy, Fudan University, Shanghai 201203 (China); Deng, Chunhui [Department of Chemistry and Institutes of Biomedical Sciences, Fudan University, Shanghai 200433 (China); Duan, Gengli [Pharmaceutical Analysis Department, School of Pharmacy, Fudan University, Shanghai 201203 (China)

    2015-06-23

    Highlights: • A new IMAC material (Fe{sub 3}O{sub 4}@PD-Nb{sup 5+}) was synthesized. • The strong magnetic behaviors of the microspheres ensure fast and easy separation. • The enrichment ability was tested by human serum and nonfat milk. • The results were compared with other IMAC materials including the commercial kits. • All results proved the good enrichment ability, especially for multiphosphopeptides. - Abstract: Rapid and selective enrichment of phosphopeptides from complex biological samples is essential and challenging in phosphorylated proteomics. In this work, for the first time, niobium ions were directly immobilized on the surface of polydopamine-coated magnetic microspheres through a facile and effective synthetic route. The Fe{sub 3}O{sub 4}@polydopamine-Nb{sup 5+} (denoted as Fe{sub 3}O{sub 4}@PD-Nb{sup 5+}) microspheres possess merits of high hydrophilicity and good biological compatibility, and demonstrated low limit of detection (2 fmol). The selectivity was also basically satisfactory (β-casein:BSA = 1:500) to capture phosphopeptides. They were also successfully applied for enrichment of phosphopeptides from real biological samples such as human serum and nonfat milk. Compared with Fe{sub 3}O{sub 4}@PD-Ti{sup 4+} microspheres, the Fe{sub 3}O{sub 4}@PD-Nb{sup 5+} microspheres exhibit superior selectivity to multi-phosphorylated peptides, and thus may be complementary to the conventional IMAC materials.

  19. Ion mass and energy selective hyperthermal ion-beam assisted deposition setup

    Science.gov (United States)

    Gerlach, J. W.; Schumacher, P.; Mensing, M.; Rauschenbach, S.; Cermak, I.; Rauschenbach, B.

    2017-06-01

    For the synthesis of high-quality thin films, ion-beam assisted deposition (IBAD) is a frequently used technique providing precise control over several substantial film properties. IBAD typically relies on the use of a broad-beam ion source. Such ion sources suffer from the limitation that they deliver a blend of ions with different ion masses, each of them possessing a certain distribution of kinetic energy. In this paper, a compact experimental setup is presented that enables the separate control of ion mass and ion kinetic energy in the region of hyperthermal energies (few 1 eV - few 100 eV). This ion energy region is of increasing interest not only for ion-assisted film growth but also for the wide field of preparative mass spectrometry. The setup consists of a constricted glow-discharge plasma beam source and a tailor-made, compact quadrupole system equipped with entry and exit ion optics. It is demonstrated that the separation of monoatomic and polyatomic nitrogen ions (N+ and N2+) is accomplished. For both ion species, the kinetic energy is shown to be selectable in the region of hyperthermal energies. At the sample position, ion current densities are found to be in the order of 1 μA/cm2 and the full width at half maximum of the ion beam profile is in the order of 10 mm. Thus, the requirements for homogeneous deposition processes in sufficiently short periods of time are fulfilled. Finally, employing the described setup, for the first time in practice epitaxial GaN films were deposited. This opens up the opportunity to fundamentally study the influence of the simultaneous irradiation with hyperthermal ions on the thin film growth in IBAD processes and to increase the flexibility of the technique.

  20. [Metal-tag labeling coupled with high performance liquid chromatography-selected ion monitoring mass spectrometry for absolute quantitation of proteins].

    Science.gov (United States)

    Li, Jiabin; Zhou, Lianqi; Yan, Hui; Li, Nannan; Hao, Feiran; Tian, Fang; Zhang, Yangjun

    2014-04-01

    A novel method has been established based on metal element chelated tags coupled with high performance liquid chromatography-selected ion monitoring mass spectrometry (HPLC-SIM/MS). The labeling efficiency and stability of metal element chelated tags, the chromatographic retention behavior and MS behavior of the labeled peptides, the linear range and accuracy of this method were examined. The results showed that the metal element chelated tag method has high labeling efficiency and high labeling stability, and the labeled peptides with different kinds of metal tags have consistent chromatographic retention behavior. The method of metal tags coupled with HPLC-SIM/MS has high sensitivity with the limit of quantification (LOQ) up to 1 fmol. The linear range for the method was between 1 fmol to 500 fmol with R2 > 0.99, which means the method has a good linearity. Moreover, this method had an average recovery of 117.01%. The method was used in the absolute quantitation of a protein enolase in Thermoanaerobacter tengcongensis (TTE) with a relative standard deviation of 5.74%, which means high precision. All the results showed that this method is accurate and reliable for the absolute quantitation of proteins. This gives us an alternative for the quantitative determination of proteins in relatively simple biological samples.

  1. Selective ion transport in functionalized carbon nanotubes

    Science.gov (United States)

    Samoylova, Olga N.; Calixte, Emvia I.; Shuford, Kevin L.

    2017-11-01

    Ion transport through functionalized carbon nanotubes in an external electric field is studied using all atom molecular dynamics simulations. The surface of carbon nanotubes has been functionalized with hydrogens and hydroxyl groups, and ionic current passing through the nanochannels has been examined with respect to the extent of surface modification. We are able to dramatically increase the ionic current passing through the nanotube via the appropriate surface modification. An analysis of the electrostatic potential within the tube shows higher ionic currents result from an increase in accessible pathways coupled with a global shift toward more direct ion passage. Moreover, through judicious choice of structure, the current can be modulated to a large degree with ion selectivity.

  2. A Schiff base complex of Zn(II) as a neutral carrier for highly selective PVC membrane sensors for the sulfate ion.

    Science.gov (United States)

    Shamsipur, M; Yousefi, M; Hosseini, M; Ganjali, M R; Sharghi, H; Naeimi, H

    2001-07-01

    Novel polymeric membrane (PME) and coated graphite (CGE) sulfate-selective electrodes based on a recently synthesized Schiff base complex of Zn(II) were prepared. The electrodes reveal a Nernstian behavior over wide SO4(2-) ion concentration ranges (5.0 x 10(-5)-1.0 x 10(-1) M for PME and 1.0 x 10(-7)-1.0 x 10(-1) M for CGE) and very low detection limits (2.8 x 10(-5) M for PME and 8.5 x 10(-8) M for CGE). The potentiometric response is independent of the pH of the solution in the pH range 3.0-7.0. The electrodes manifest advantages of low resistance, very fast response, and, most importantly, good selectivities relative to a wide variety of other anions. In fact, the selectivity behavior of the proposed SO4(2) ion-selective electrodes shows a great improvement compared to the previously reported electrodes for sulfate ion. The electrodes can be used for at least 3 months without any appreciable divergence in potentials. The electrodes were used as an indicator electrode in the potentiometric titration of sulfate and barium ions and in the determination of iron in ferrous sulfate tablets.

  3. Ion-Exchange-Induced Selective Etching for the Synthesis of Amino-Functionalized Hollow Mesoporous Silica for Elevated-High-Temperature Fuel Cells

    DEFF Research Database (Denmark)

    Zhang, Jin; Liu, Jian; Lu, Shanfu

    2017-01-01

    As differentiated from conventional synthetic processes, amino-functionalized hollow mesoporous silica (NH2–HMS) has been synthesized using a new and facile strategy of ion-exchange-induced selective etching of amino-functionalized mesoporous silica (NH2-meso-silica) by an alkaline solution. Nucl...

  4. Facile synthesis of gallium ions immobilized and adenosine functionalized magnetic nanoparticles with high selectivity for multi-phosphopeptides.

    Science.gov (United States)

    Zhang, Liyuan; Liang, Zhen; Zhang, Lihua; Zhang, Yukui; Shao, Shujuan

    2015-11-05

    Despite recent advances in phosphoproteome research, detection and characterization of multi-phosphopeptides have remained a challenge. Here we present a novel IMAC strategy for effective extracting multi-phosphopeptides from complex samples, through Ga(3+) chelation to the adenosine tri-phosphate (ATP)-functionalized magnetic nanoparticles (Ga(3+)-ATP-MNPs). The high specificity of Ga(3+)-ATP-MNPs was demonstrated by efficient enriching multi-phosphopeptides from the digest mixture of β-casein and BSA with molar ratio as low as 1:5000. Ga(3+)-ATP-MNPs were also successfully applied for the phosphoproteome analysis of rat liver mitochondria, resulting in the identification of 193 phosphopeptides with 331 phosphorylation sites from 158 phosphoproteins. In other words, 54.4% of the phosphopeptides trapped by Ga(3+)-ATP-MNPs were observed with more than one phosphorylated sites, resulting in significant improvement on the identification of peptides with multi-phosphorylated sites. The high specificity of Ga(3+)-ATP-MNPs towards multi-phosphopeptides may be due to the synergistic effect of the strong hydrophilic surface functionalized by ATP and the proper chelating strength provided by Ga(3+). Moreover, the unique magnetic core of Ga(3+)-ATP-MNPs also facilitates the isolation process and on-plate enrichment for direct MALDI MS analysis with limit of detection as low as 30 amol. This new affinity-based protocol is expected to provide a powerful approach for characterizing multiple phosphorylation sites on proteins in complex and dilute analytes, which may be explored as complementary technique for improving the coverage of phosphoproteome. Copyright © 2015 Elsevier B.V. All rights reserved.

  5. Efficient ensemble system based on the copper binding motif for highly sensitive and selective detection of cyanide ions in 100% aqueous solutions by fluorescent and colorimetric changes.

    Science.gov (United States)

    Jung, Kwan Ho; Lee, Keun-Hyeung

    2015-09-15

    A peptide-based ensemble for the detection of cyanide ions in 100% aqueous solutions was designed on the basis of the copper binding motif. 7-Nitro-2,1,3-benzoxadiazole-labeled tripeptide (NBD-SSH, NBD-SerSerHis) formed the ensemble with Cu(2+), leading to a change in the color of the solution from yellow to orange and a complete decrease of fluorescence emission. The ensemble (NBD-SSH-Cu(2+)) sensitively and selectively detected a low concentration of cyanide ions in 100% aqueous solutions by a colorimetric change as well as a fluorescent change. The addition of cyanide ions instantly removed Cu(2+) from the ensemble (NBD-SSH-Cu(2+)) in 100% aqueous solutions, resulting in a color change of the solution from orange to yellow and a "turn-on" fluorescent response. The detection limits for cyanide ions were lower than the maximum allowable level of cyanide ions in drinking water set by the World Health Organization. The peptide-based ensemble system is expected to be a potential and practical way for the detection of submicromolar concentrations of cyanide ions in 100% aqueous solutions.

  6. Tuning the ion selectivity of two-pore channels

    Energy Technology Data Exchange (ETDEWEB)

    Guo, Jiangtao; Zeng, Weizhong; Jiang, Youxing (UTSMC)

    2017-01-17

    Organellar two-pore channels (TPCs) contain two copies of a Shaker-like six-transmembrane (6-TM) domain in each subunit and are ubiquitously expressed in plants and animals. Interestingly, plant and animal TPCs share high sequence similarity in the filter region, yet exhibit drastically different ion selectivity. Plant TPC1 functions as a nonselective cation channel on the vacuole membrane, whereas mammalian TPC channels have been shown to be endo/lysosomal Na+-selective or Ca2+-release channels. In this study, we performed systematic characterization of the ion selectivity of TPC1 from Arabidopsis thaliana (AtTPC1) and compared its selectivity with the selectivity of human TPC2 (HsTPC2). We demonstrate that AtTPC1 is selective for Ca2+ over Na+, but nonselective among monovalent cations (Li+, Na+, and K+). Our results also confirm that HsTPC2 is a Na+-selective channel activated by phosphatidylinositol 3,5-bisphosphate. Guided by our recent structure of AtTPC1, we converted AtTPC1 to a Na+-selective channel by mimicking the selectivity filter of HsTPC2 and identified key residues in the TPC filters that differentiate the selectivity between AtTPC1 and HsTPC2. Furthermore, the structure of the Na+-selective AtTPC1 mutant elucidates the structural basis for Na+ selectivity in mammalian TPCs.

  7. Highly selective and sensitive colorimetric determination of Cr3 + ion by 4-amino-5-methyl-4H-1,2,4-triazole-3-thiol functionalized Au nanoparticles

    Science.gov (United States)

    Shahrivari, Shima; Faridbod, Farnoush; Ganjali, Mohammad Reza

    2018-02-01

    In this work, a rapid, selective naked eyes colorimetric chemical probe for the detection of Cr3 + was developed based on functionalization of gold nanoparticles. For this purpose, surface of Au NPs was functionalized using 4-amino-5-methyl-4H-1,2,4-triazole-3-thiol (AMTT). Through colorimetric studies, it was found that in the presence of Cr3 + ions, AMTT-Au NPs instantly aggregated and resulted in a color change of the solution from red to blue. The color change of AMTT-Au NPs due to the aggregation induced by Cr3 + can be seen with even naked eyes and also by UV-Vis spectroscopy with a detection limit of 1.8 μM and 0.1 μM, respectively. AMTT-Au NPs showed excellent selectivity toward Cr3 + compared to other cations tested, including K+, Na+, Cs+, Fe3 +, Ni2 +, Cu2 +, Co2 +, Zn2 +, Ba2 +, Ca2 +, Mg2 +, Cd2 +, Pb2 +, Hg2 + ions and especially all trivalent lanthanide ions. The absorbance ratio (A650/A525) was linear toward Cr3 + concentrations in the range of 0.6-6.1 μM (R2 = 0.996). The best response was achieved over a pH range of 3-5. Furthermore, the proposed colorimetric method based on AMTT-Au NPs was successfully used for Cr3 + ion detection in plasma sample and some water samples.

  8. A new and highly selective turn-on fluorescent sensor with fast response time for the monitoring of cadmium ions in cosmetic, and health product samples

    Science.gov (United States)

    Khani, Rouhollah; Ghiamati, Ebrahim; Boroujerdi, Ramin; Rezaeifard, Abdolreza; Zaryabi, Mohadeseh Hosseinpour

    2016-06-01

    Cadmium (Cd) which is an extremely toxic could be found in many products like plastics, fossil fuel combustion, cosmetics, water resources, and wastewaters. It is capable of causing serious environmental and health problems such as lung, prostate, renal cancers and the other disorders. So, the development of a sensor to continually monitor cadmium is considerably demanding. Tetrakis(4-nitrophenyl)porphyrin, T(4-NO2-P)P, was synthesized and used as a new and highly selective fluorescent probe for monitoring cadmium ions in the "turn-on" mode. There was a linear relationship between fluorescence intensity and the concentration of Cd(II) in the range of 1.0 × 10- 6 to 1.0 × 10- 5 mol L- 1 with a detection limit of 0.276 μM. To examine the most important parameters involved and their interactions in the sensor optimization procedure, a four-factor central composite design (CCD) combined with response surface modeling (RSM) was implemented. The practical applicability of the developed sensor was investigated using real cosmetic, and personal care samples.

  9. A new and highly selective turn-on fluorescent sensor with fast response time for the monitoring of cadmium ions in cosmetic, and health product samples.

    Science.gov (United States)

    Khani, Rouhollah; Ghiamati, Ebrahim; Boroujerdi, Ramin; Rezaeifard, Abdolreza; Zaryabi, Mohadeseh Hosseinpour

    2016-06-15

    Cadmium (Cd) which is an extremely toxic could be found in many products like plastics, fossil fuel combustion, cosmetics, water resources, and wastewaters. It is capable of causing serious environmental and health problems such as lung, prostate, renal cancers and the other disorders. So, the development of a sensor to continually monitor cadmium is considerably demanding. Tetrakis(4-nitrophenyl)porphyrin, T(4-NO2-P)P, was synthesized and used as a new and highly selective fluorescent probe for monitoring cadmium ions in the "turn-on" mode. There was a linear relationship between fluorescence intensity and the concentration of Cd(II) in the range of 1.0×10(-6) to 1.0×10(-5)molL(-1) with a detection limit of 0.276μM. To examine the most important parameters involved and their interactions in the sensor optimization procedure, a four-factor central composite design (CCD) combined with response surface modeling (RSM) was implemented. The practical applicability of the developed sensor was investigated using real cosmetic, and personal care samples. Copyright © 2016 Elsevier B.V. All rights reserved.

  10. Highly Selective Bifunctional Luminescent Sensor toward Nitrobenzene and Cu2+ Ion Based on Microporous Metal-Organic Frameworks: Synthesis, Structures, and Properties.

    Science.gov (United States)

    Yang, Lirong; Lian, Chen; Li, Xuefei; Han, Yuyang; Yang, Lele; Cai, Ting; Shao, Caiyun

    2017-05-24

    Two metal-organic frameworks (MOFs), namely, [Ni(DTP)(H2O)]n (I) and [Cd2(DTP)2(bibp)1.5]n (II) (H2DPT = 4'-(4-(3,5-dicarboxylphenoxy) phenyl)-4,2':6',4″-terpyridine; bibp = 1,3-di(1H-imidazol-1-yl)propane), that present structural diversity were solvothermally prepared. Single-crystal X-ray diffraction analysis indicates that they consist of {NiN2O4} building units (for I) and {CdO4N2} and {CdO3N3} building units (for II), which are further linked by multicarboxylate H2DPT to construct microporous three-dimensional frameworks. The remarkable character of these frameworks is that coordination polymer II demonstrates highly selective and sensitive bifunctional luminescent sensor toward nitrobenzene and Cu2+ ion. The fluorescence quenching mechanism of II caused by nitrobenzene is ascribed to electron transfer from electron-rich (II) to electron-deficient nitrobenzene. The result was also evidenced by the density functional theory. Furthermore, anti-ferromagnetic as well as electrochemical characters of Ni-MOF (I) were also investigated in this paper.

  11. Ion selective electrodes in environmental analysis

    Directory of Open Access Journals (Sweden)

    Radu Aleksandar

    2013-01-01

    Full Text Available An overview is given dealing with application of ion-selective electrodes (ISEs in environmental analysis. ISEs are placed into the context of the trend of development of sensors for extensive and frequent monitoring. Discussed are the issues such as sensing platforms and their mass-production, improvement of precision, diagnostic of sensor’s functionality, and development of reference electrodes and several examples of real-life application of ISEs in environmental analysis are given. The main emphasis of this article is directed towards summarizing recent of authors’ results during the past several years.

  12. Ion-Exchange-Induced Selective Etching for the Synthesis of Amino-Functionalized Hollow Mesoporous Silica for Elevated-High-Temperature Fuel Cells.

    Science.gov (United States)

    Zhang, Jin; Liu, Jian; Lu, Shanfu; Zhu, Haijin; Aili, David; De Marco, Roland; Xiang, Yan; Forsyth, Maria; Li, Qingfeng; Jiang, San Ping

    2017-09-20

    As differentiated from conventional synthetic processes, amino-functionalized hollow mesoporous silica (NH2-HMS) has been synthesized using a new and facile strategy of ion-exchange-induced selective etching of amino-functionalized mesoporous silica (NH2-meso-silica) by an alkaline solution. Nuclear magnetic resonance (NMR) spectroscopy and in situ time-resolved small-angle X-ray scattering (SAXS) reveal that ion-exchange-induced selective etching arises from the gradient distribution of OH- in the NH2-meso-silica nanospheres. Moreover, the ion-exchange-induced selective etching mechanism is verified through a successful synthesis of hollow mesoporous silica. After infiltration with phosphotungstic acid (PWA), PWA-NH2-HMS nanoparticles are dispersed in the poly(ether sulfone)-polyvinylpyrrolidone (PES-PVP) matrix, forming a hybrid PWA-NH2-HMS/PES-PVP nanocomposite membrane. The resultant nanocomposite membrane with an optimum loading of 10 wt % of PWA-NH2-HMS showed an enhanced proton conductivity of 0.175 S cm-1 and peak power density of 420 mW cm-2 at 180 °C under anhydrous conditions. Excellent durability of the hybrid composite membrane fuel cell has been demonstrated at 200 °C. The results of this study demonstrated the potential of the facile synthetic strategy in the fabrication of NH2-HMS with controlled mesoporous structure for application in nanocomposite membranes as a technology platform for elevated-temperature proton exchange membrane fuel cells.

  13. Real time measurement of cytoplasmic ions with ion-selective microelectrodes.

    Science.gov (United States)

    Miller, Anthony J

    2013-01-01

    Ion-selective microelectrodes can be used to report intracellular ion concentrations. The ion-selective barrels of microelectrodes are filled with a sensor cocktail containing several different components including an ion-selective molecule, sensor or exchanger, a solvent or plasticizer, lipophilic cation/anion additives, and a matrix to solidify the membrane. For many ions, the readymade membrane cocktail can be purchased, but the individual chemical components can be bought from suppliers and mixing the cocktail saves money. For commercially available liquid membrane cocktails the membrane matrix is often not included. For plants a matrix is essential for intracellular impalements because without it cell turgor will displace the liquid membrane from the electrode tip, giving decreased or even lost sensitivity. The matrix frequently used is a high molecular weight poly(vinyl chloride). This addition increases the electrical resistance of the electrode, slowing the response time of the electrode. The use of multi-barreled electrodes enables the identification of the cellular compartment. For example, the inclusion of a pH-selective electrode enables the cytoplasm and vacuole to be distinguished.

  14. The Generation of Dehydroalanine Residues in Protonated Polypeptides: Ion/Ion Reactions for Introducing Selective Cleavages

    Science.gov (United States)

    Peng, Zhou; Bu, Jiexun; McLuckey, Scott A.

    2017-09-01

    We examine a gas-phase approach for converting a subset of amino acid residues in polypeptide cations to dehydroalanine (Dha). Subsequent activation of the modified polypeptide ions gives rise to specific cleavage N-terminal to the Dha residue. This process allows for the incorporation of selective cleavages in the structural characterization of polypeptide ions. An ion/ion reaction within the mass spectrometer between a multiply protonated polypeptide and the sulfate radical anion introduces a radical site into the multiply protonated polypeptide reactant. Subsequent collisional activation of the polypeptide radical cation gives rise to radical side chain loss from one of several particular amino acid side chains (e.g., leucine, asparagine, lysine, glutamine, and glutamic acid) to yield a Dha residue. The Dha residues facilitate preferential backbone cleavages to produce signature c- and z-ions, demonstrated with cations derived from melittin, mechano growth factor (MGF), and ubiquitin. The efficiencies for radical side chain loss and for subsequent generation of specific c- and z-ions have been examined as functions of precursor ion charge state and activation conditions using cations of ubiquitin as a model for a small protein. It is noted that these efficiencies are not strongly dependent on ion trap collisional activation conditions but are sensitive to precursor ion charge state. Moderate to low charge states show the greatest overall yields for the specific Dha cleavages, whereas small molecule losses (e.g., water/ammonia) dominate at the lowest charge states and proton catalyzed amide bond cleavages that give rise to b- and y-ions tend to dominate at high charge states. [Figure not available: see fulltext.

  15. Clotrimazole-triiodide ion association as an ion exchanger for a triiodide ion-selective electrode.

    Science.gov (United States)

    Farhadi, Khalil; Maleki, Ramin

    2002-02-01

    A novel triiodide ion-selective electrode based on a clotrimazole-triiodide ion pair as a membrane carrier was prepared. It has a linear response to triiodide from 8 x 10(-6) to 5 x 10(-3) M with a slope of -68.9 mV per decade and a detection limit of 5 x 10(-6) M. The electrode response is independent of the pH of the solution in the pH range 2-9. It has a very short response time and can be used for at least 3 months without any considerable divergence in the potentials. The proposed sensor revealed very good selectivities for I3- over a variety of other anions. It was used as an indicator electrode in the potentiometric titration of triiodide ions and in an indirect potentiometric determination of clotrimazole in pharmaceutical preparations.

  16. A highly selective chromogenic sensor for Mn2 +, turn-off fluorometric for Hg2 + ion, and turn-on fluorogenic sensor for F- ion with the practical application

    Science.gov (United States)

    Gupta, Neha; Singhal, Divya; Singh, Ashok Kumar; Singh, Neetu; Singh, U. P.

    2017-04-01

    A colorimetric and fluorometric probe (E)-2-((8-hydroxy-1,2,3,5,6,7-hexahydropyrido[3,2,1-ij]quinolin-9-yl)methylene)hydrazinecarbothioamide based on thiosemicarbazide and julolidine moieties has been synthesised in pure crystalline form and characterized by 1H NMR, UV-vis, elemental analysis and single crystal XRD. The probe functioned as multitarget ion sensor, detect biologically important metal ions Hg2 + and Mn2 + in dual channel mode. Meanwhile, in mixed solvent media DMF/H2O [8:2], probe displayed selectivity for Hg2 + over other cations by the emission spectrum. Interestingly probe has been explored to recognize F- anion in DMF through ESIPT mechanism. The 1:1 binding stoichiometry of probe with Hg2 + and Mn2 + is confirmed by Job's plot through emission titration and UV-vis titration respectively. Probe is selective and sensitive to Hg2 + and Mn2 + with detection limit as low as 15 μM and 0.2 μM respectively. The sensing mechanism for selective ions was also scrutinized using 1H NMR experiments and computational studies.

  17. A novel PVC-membrane optical sensor for highly sensitive and selective determination of UO 22+ ion based on a recently synthesized benzo-substituted macrocyclic diamide and dibenzoylmethane

    Science.gov (United States)

    Shamsipur, Mojtaba; Zargoosh, Kiomars; Mizani, Farhang; Eshghi, Hossein; Rostami, Faramarz

    2010-09-01

    A highly sensitive ion-selective bulk optode membrane for sensing UO 22+ ion based on plasticized poly(vinyl chloride) containing 6,7,9,10,12,13,15,16,23,24,25,26-dodecahydrodibenzo[n,v][1,4,7,10,13,17,20]pentaoxa-diazacyclotricosine-22,27-dione as ionophore, dibenzodylmethane as chromoionophore and sodium tetraphenylborate as an ionic additive was prepared. In addition to its high stability, reproducibility and relatively long lifetime, the proposed optical sensor revealed good selectivity for uranyl ion over a large number of alkali, alkaline earth, transition, and heavy metal ions. The proposed sensor displays a calibration response for UO 22+ over a concentration range of 4.3 × 10 -6 to 2.5 × 10 -8 M with a limit of detection of 8.0 × 10 -9 M and a response time of less than 12 min. The proposed optical sensor was applied successfully to the determination of UO 22+ ion in tap water and Khoshumi mine concentrated solution samples.

  18. Quantum Interference and Selectivity through Biological Ion Channels.

    Science.gov (United States)

    Salari, Vahid; Naeij, Hamidreza; Shafiee, Afshin

    2017-01-30

    The mechanism of selectivity in ion channels is still an open question in biology for more than half a century. Here, we suggest that quantum interference can be a solution to explain the selectivity mechanism in ion channels since interference happens between similar ions through the same size of ion channels. In this paper, we simulate two neighboring ion channels on a cell membrane with the famous double-slit experiment in physics to investigate whether there is any possibility of matter-wave interference of ions via movement through ion channels. Our obtained decoherence timescales indicate that the quantum states of ions can only survive for short times, i.e. ≈100 picoseconds in each channel and ≈17-53 picoseconds outside the channels, giving the result that the quantum interference of ions seems unlikely due to environmental decoherence. However, we discuss our results and raise few points, which increase the possibility of interference.

  19. Quantum Interference and Selectivity through Biological Ion Channels

    Science.gov (United States)

    Salari, Vahid; Naeij, Hamidreza; Shafiee, Afshin

    2017-01-01

    The mechanism of selectivity in ion channels is still an open question in biology for more than half a century. Here, we suggest that quantum interference can be a solution to explain the selectivity mechanism in ion channels since interference happens between similar ions through the same size of ion channels. In this paper, we simulate two neighboring ion channels on a cell membrane with the famous double-slit experiment in physics to investigate whether there is any possibility of matter-wave interference of ions via movement through ion channels. Our obtained decoherence timescales indicate that the quantum states of ions can only survive for short times, i.e. ≈100 picoseconds in each channel and ≈17–53 picoseconds outside the channels, giving the result that the quantum interference of ions seems unlikely due to environmental decoherence. However, we discuss our results and raise few points, which increase the possibility of interference. PMID:28134331

  20. Application of an Hg2+ selective imprinted polymer as a new modifying agent for the preparation of a novel highly selective and sensitive electrochemical sensor for the determination of ultratrace mercury ions.

    Science.gov (United States)

    Alizadeh, Taher; Ganjali, Mohamad Reza; Zare, Mashaalah

    2011-03-09

    A simple and very selective electrode, based on a mercury ion imprinted polymer (IIP), and its application for the determination of Hg(2+) ions in the real samples is introduced. Mercury ion selective cavities were created in the vinyl pyridine based cross-linked polymer. In order to fabricate the sensor carbon particles and polymer powder were mixed with melted n-eicosane. An explicit difference was observed between the responses of the electrodes modified with IIP and non imprinted polymer (NIP), indicating proper performance of the recognition sites of the IIP. Various factors, known to affect the response behavior of selective electrode, were investigated and optimized. The interference of different ionic species with the response of the electrode was also studied. The results revealed that, compared to previously developed mercury selective sensors, the proposed sensor was more selective, regarding the common potential interferer. This sensor showed a linear response range of 2.5 × 10(-9)-5.0 × 10(-7) M and lower detection limit of 5.2 × 10(-10) M (S/N). The sensor was successfully applied to the determination of mercury in real samples. Copyright © 2011. Published by Elsevier B.V.

  1. Determination of Nd3+ Ions in Solution Samples by a Coated Wire Ion-Selective Sensor

    Directory of Open Access Journals (Sweden)

    Hassan Ali Zamani

    2012-01-01

    Full Text Available A new coated wire electrode (CWE using 5-(methylsulfanyl-3-phenyl-1H-1,2,4-triazole (MPT as an ionophore has been developed as a neodymium ion-selective sensor. The sensor exhibits Nernstian response for the Nd3+ ions in the concentration range of 1.0×10−6-1.0×10−2 M with detection limit of 3.7×10−7 M. It displays a Nernstian slope of 20.2±0.2 mV/decade in the pH range of 2.7–8.1. The proposed sensor also exhibits a fast response time of ∼5 s. The sensor revealed high selectivity with respect to all common alkali, alkaline earth, transition and heavy metal ions, including members of the lanthanide family other than Nd3+. The electrode was used as an indicator electrode in the potentiometric titration of Nd(III ions with EDTA. The electrode was also employed for the determination of the Nd3+ ions concentration in water solution samples.

  2. The emerging role of ion/ion reactions in biological mass spectrometry: considerations for reagent ion selection.

    Science.gov (United States)

    McLuckey, Scott A

    2010-01-01

    The advent of ionization methods that can produce multiply charged gaseous ions has enabled the development of gas-phase ion/ion reactions in analytical mass spectrometry. Ion/ion chemistry has proved to be a particularly effective means for converting ions from one type to another and allows for a decoupling of the ionization method from the nature of the ion subjected to tandem mass spectrometry. A growing array of applications has been developed based on a variety of reaction types, including electron transfer, proton transfer, charge inversion, metal transfer, etc. Most ion/ion reactions take place following the formation of a stable bound orbit between the reactants. As reactants approach closely enough for chemistry to occur, they can react by small charged particle transfer (i.e. electron transfer and proton transfer) at crossing points in the interaction potential. Alternatively, the reactants can collide to form a relatively long-lived complex. A wide range of chemical reactions can result from the long-lived complex, which include multiple charged particle transfers and covalent bond formation. For a given analyte ion, the major reaction pathway is determined by the characteristics of the reagent ion. An appreciation of the factors that underlie the partitioning of ion/ion reaction products is important in the design and selection of reagent ions to effect transformations of interest. Important considerations for reagent ion selection are discussed here within the context of a generalized scheme for ion/ion reaction dynamics.

  3. Highly Stripped Ion Sources for MeV Ion Implantation

    Energy Technology Data Exchange (ETDEWEB)

    Hershcovitch, Ady

    2009-06-30

    Original technical objectives of CRADA number PVI C-03-09 between BNL and Poole Ventura, Inc. (PVI) were to develop an intense, high charge state, ion source for MeV ion implanters. Present day high-energy ion implanters utilize low charge state (usually single charge) ion sources in combination with rf accelerators. Usually, a MV LINAC is used for acceleration of a few rnA. It is desirable to have instead an intense, high charge state ion source on a relatively low energy platform (de acceleration) to generate high-energy ion beams for implantation. This de acceleration of ions will be far more efficient (in energy utilization). The resultant implanter will be smaller in size. It will generate higher quality ion beams (with lower emittance) for fabrication of superior semiconductor products. In addition to energy and cost savings, the implanter will operate at a lower level of health risks associated with ion implantation. An additional aim of the project was to producing a product that can lead to long­ term job creation in Russia and/or in the US. R&D was conducted in two Russian Centers (one in Tomsk and Seversk, the other in Moscow) under the guidance ofPVI personnel and the BNL PI. Multiple approaches were pursued, developed, and tested at various locations with the best candidate for commercialization delivered and tested at on an implanter at the PVI client Axcelis. Technical developments were exciting: record output currents of high charge state phosphorus and antimony were achieved; a Calutron-Bemas ion source with a 70% output of boron ion current (compared to 25% in present state-of-the-art). Record steady state output currents of higher charge state phosphorous and antimony and P ions: P{sup 2+} (8.6 pmA), P{sup 3+} (1.9 pmA), and P{sup 4+} (0.12 pmA) and 16.2, 7.6, 3.3, and 2.2 pmA of Sb{sup 3+} Sb {sup 4 +}, Sb{sup 5+}, and Sb{sup 6+} respectively. Ultimate commercialization goals did not succeed (even though a number of the products like high

  4. Ion-Selective Detection with Glass Nanopipette for Living Cells

    Science.gov (United States)

    Takami, T.; Son, J. W.; Kang, E. J.; Deng, X. L.; Kawai, T.; Lee, S.-W.; Park, B. H.

    2013-05-01

    We developed a method to probe local ion concentration with glass nanopipette in which poly(vinyl chloride) membrane containing ionophore for separate ion detection is prepared. Here we demonstrate how ion-selective detections are available for living cells such as HeLa cell, rat vascular myocyte, and neuron cell.

  5. Carbon Nanotube-Based Ion Selective Sensors for Wearable Applications.

    Science.gov (United States)

    Roy, Soumyendu; David-Pur, Moshe; Hanein, Yael

    2017-10-11

    Wearable electronics offer new opportunities in a wide range of applications, especially sweat analysis using skin sensors. A fundamental challenge in these applications is the formation of sensitive and stable electrodes. In this article we report the development of a wearable sensor based on carbon nanotube (CNT) electrode arrays for sweat sensing. Solid-state ion selective electrodes (ISEs), sensitive to Na(+) ions, were prepared by drop coating plasticized poly(vinyl chloride) (PVC) doped with ionophore and ion exchanger on CNT electrodes. The ion selective membrane (ISM) filled the intertubular spaces of the highly porous CNT film and formed an attachment that was stronger than that achieved with flat Au, Pt, or carbon electrodes. Concentration of the ISM solution used influenced the attachment to the CNT film, the ISM surface morphology, and the overall performance of the sensor. Sensitivity of 56 ± 3 mV/decade to Na(+) ions was achieved. Optimized solid-state reference electrodes (REs), suitable for wearable applications, were prepared by coating CNT electrodes with colloidal dispersion of Ag/AgCl, agarose hydrogel with 0.5 M NaCl, and a passivation layer of PVC doped with NaCl. The CNT-based REs had low sensitivity (-1.7 ± 1.2 mV/decade) toward the NaCl solution and high repeatability and were superior to bare Ag/AgCl, metals, carbon, and CNT films, reported previously as REs. CNT-based ISEs were calibrated against CNT-based REs, and the short-term stability of the system was tested. We demonstrate that CNT-based devices implemented on a flexible support are a very attractive platform for future wearable technology devices.

  6. Resonance ionization for the detection and for the production of radioactive ion beams. From the highly selective ultra-trace detection to the selective on-line laser ion source; Resonanzionisation zum Nachweis und zur Erzeugung radioaktiver Ionenstrahlen. Vom hochselektiven Ultraspurennachweis zur selektiven on-line Laserionenquelle

    Energy Technology Data Exchange (ETDEWEB)

    Geppert, C.

    2005-09-23

    Resonant laser ionization has been established as a universal technique for applications, which require a selective ionization and high efficiency. In this thesis two laser systems were developed and applied to attain different objectives. The first part describes the development of high resolution resonance ionization mass spectrometry (RIMS) for the ultra-trace analysis of {sup 41}Ca. Therefore three continuous diode lasers were combined with a quadrupole mass spectrometer. At an efficiency of 1 x 10{sup -5} a detection level of 2 x 10{sup -13} {sup 41}Ca/{sup tot}Ca was achieved. The method allowed the participation in an interdisciplinary osteoporosis research network. Intercomparison measurements demonstrated an excellent agreement between RIMS and all other present {sup 41}Ca ultra-trace analysis methods. The second part of the thesis refers to the adaptation of a tunable, high repetition rate titanium:sapphire laser system for the selective production of radioactive ion beams at a laser ion source, making an efficient resonant excitation of the majority of the elements of the periodic system possible. Hence a combined frequency doubling and tripling unit was constructed. The applicability of the solid-state laser system was demonstrated in off-line measurements at Mainz and on the ISOL facilities at TRIUMF and ORNL and resulted in the first on-line run at TRIUMF. (Orig.)

  7. High Current Ion Sources and Injectors for Heavy Ion Fusion

    Energy Technology Data Exchange (ETDEWEB)

    Kwan, Joe W.

    2005-02-15

    Heavy ion beam driven inertial fusion requires short ion beam pulses with high current and high brightness. Depending on the beam current and the number of beams in the driver system, the injector can use a large diameter surface ionization source or merge an array of small beamlets from a plasma source. In this paper, we review the scaling laws that govern the injector design and the various ion source options including the contact ionizer, the aluminosilicate source, the multicusp plasma source, and the MEVVA source.

  8. 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.

  9. High Resolution Scanning Ion Microscopy

    NARCIS (Netherlands)

    Castaldo, V.

    2011-01-01

    The structure of the thesis is the following. The first chapter is an introduction to scanning microscopy, where the path that led to the Focused Ion Beam (FIB) is described and the main differences between electrons and ion beams are highlighted. Chapter 2 is what is normally referred to (which I

  10. Tuning the Solid Electrolyte Interphase for Selective Li- and Na-Ion Storage in Hard Carbon

    Energy Technology Data Exchange (ETDEWEB)

    Soto, Fernando A. [Department of Chemical Engineering, Texas A& M University, College Station TX 77843-3122 USA; Yan, Pengfei [Pacific Northwest National Laboratory, 902 Battelle Boulevard Richland WA 99354 USA; Engelhard, Mark H. [Pacific Northwest National Laboratory, 902 Battelle Boulevard Richland WA 99354 USA; Marzouk, Asma [Qatar Environment and Energy Research Institute, Hamad Bin Khalifa University, P.O. Box 5825 Doha Qatar; Wang, Chongmin [Pacific Northwest National Laboratory, 902 Battelle Boulevard Richland WA 99354 USA; Xu, Guiliang [Chemical Sciences and Engineering Division, Argonne National Laboratory, 9700 South Cass Avenue Argonne IL 60439 USA; Chen, Zonghai [Chemical Sciences and Engineering Division, Argonne National Laboratory, 9700 South Cass Avenue Argonne IL 60439 USA; Amine, Khalil [Chemical Sciences and Engineering Division, Argonne National Laboratory, 9700 South Cass Avenue Argonne IL 60439 USA; Liu, Jun [Pacific Northwest National Laboratory, 902 Battelle Boulevard Richland WA 99354 USA; Sprenkle, Vincent L. [Pacific Northwest National Laboratory, 902 Battelle Boulevard Richland WA 99354 USA; El-Mellouhi, Fedwa [Qatar Environment and Energy Research Institute, Hamad Bin Khalifa University, P.O. Box 5825 Doha Qatar; Balbuena, Perla B. [Department of Chemical Engineering, Texas A& M University, College Station TX 77843-3122 USA; Li, Xiaolin [Pacific Northwest National Laboratory, 902 Battelle Boulevard Richland WA 99354 USA

    2017-03-07

    Solid-electrolyte interphase (SEI) with controllable properties are highly desirable to improve battery performance. In this paper, we use a combined experimental and simulation approach to study the SEI formation on hard carbon in Li and Na-ion batteries. We show that with proper additives, stable SEI can be formed on hard carbon by pre-cycling the electrode materials in Li or Na-ion electrolyte. Detailed mechanistic studies suggest that the ion transport in the SEI layer is kinetically controlled and can be tuned by the applied voltage. Selective Na and Li-ion SEI membranes are produced using the Na or Li-ion based electrolytes respectively. The large Na ion SEI allows easy transport of Li ions, while the small Li ion SEI shuts off the Na-ion transport. Na-ion storage can be manipulated by tuning the SEI with film-forming electrolyte additives or preforming a SEI on the electrodes’ surface. The Na specific capacity can be controlled to <25 mAh/g, ~1/10 of the normal capacity (250 mAh/g). Unusual selective/preferential transport of Li-ion is demonstrated by preforming a SEI on the electrode’s surface and corroborated with a mixed electrolyte. This work may provide new guidance for preparing good ion selective conductors using electrochemical approaches in the future.

  11. T-type channels become highly permeable to sodium ions using an alternative extracellular turret region (S5-P) outside the selectivity filter.

    Science.gov (United States)

    Senatore, Adriano; Guan, Wendy; Boone, Adrienne N; Spafford, J David

    2014-04-25

    T-type (Cav3) channels are categorized as calcium channels, but invertebrate ones can be highly sodium-selective channels. We illustrate that the snail LCav3 T-type channel becomes highly sodium-permeable through exon splicing of an extracellular turret and descending helix in domain II of the four-domain Cav3 channel. Highly sodium-permeable T-type channels are generated without altering the invariant ring of charged residues in the selectivity filter that governs calcium selectivity in calcium channels. The highly sodium-permeant T-type channel expresses in the brain and is the only splice isoform expressed in the snail heart. This unique splicing of turret residues offers T-type channels a capacity to serve as a pacemaking sodium current in the primitive heart and brain in lieu of Nav1-type sodium channels and to substitute for voltage-gated sodium channels lacking in many invertebrates. T-type channels would also contribute substantially to sodium leak conductances at rest in invertebrates because of their large window currents.

  12. Selective Thallium (I Ion Sensor Based on Functionalised ZnO Nanorods

    Directory of Open Access Journals (Sweden)

    Z. H. Ibupoto

    2012-01-01

    Full Text Available Well controlled in length and highly aligned ZnO nanorods were grown on the gold-coated glass substrate by hydrothermal growth method. ZnO nanorods were functionalised with selective thallium (I ion ionophore dibenzyldiaza-18-crown-6 (DBzDA18C6. The thallium ion sensor showed wide linear potentiometric response to thallium (I ion concentrations ( M to  M with high sensitivity of 36.87 ± 1.49 mV/decade. Moreover, thallium (I ion demonstrated fast response time of less than 5 s, high selectivity, reproducibility, storage stability, and negligible response to common interferents. The proposed thallium (I ion-sensor electrode was also used as an indicator electrode in the potentiometric titration, and it has shown good stoichiometric response for the determination of thallium (I ion.

  13. Monitoring Ion Activities In and Around Cells Using Ion-Selective Liquid-Membrane Microelectrodes

    Directory of Open Access Journals (Sweden)

    Mark D. Parker

    2013-01-01

    Full Text Available Determining the effective concentration (i.e., activity of ions in and around living cells is important to our understanding of the contribution of those ions to cellular function. Moreover, monitoring changes in ion activities in and around cells is informative about the actions of the transporters and/or channels operating in the cell membrane. The activity of an ion can be measured using a glass microelectrode that includes in its tip a liquid-membrane doped with an ion-selective ionophore. Because these electrodes can be fabricated with tip diameters that are less than 1 μm, they can be used to impale single cells in order to monitor the activities of intracellular ions. This review summarizes the history, theory, and practice of ion-selective microelectrode use and brings together a number of classic and recent examples of their usefulness in the realm of physiological study.

  14. Electron capture by highly charged ions from surfaces and gases

    Energy Technology Data Exchange (ETDEWEB)

    Allen, F.

    2008-01-11

    In this study highly charged ions produced in Electron Beam Ion Traps are used to investigate electron capture from surfaces and gases. The experiments with gas targets focus on spectroscopic measurements of the K-shell x-rays emitted at the end of radiative cascades following electron capture into Rydberg states of Ar{sup 17+} and Ar{sup 18+} ions as a function of collision energy. The ions are extracted from an Electron Beam Ion Trap at an energy of 2 keVu{sup -1}, charge-selected and then decelerated down to 5 eVu{sup -1} for interaction with an argon gas target. For decreasing collision energies a shift to electron capture into low orbital angular momentum capture states is observed. Comparative measurements of the K-shell x-ray emission following electron capture by Ar{sup 17+} and Ar{sup 18+} ions from background gas in the trap are made and a discrepancy in the results compared with those from the extraction experiments is found. Possible explanations are discussed. For the investigation of electron capture from surfaces, highly charged ions are extracted from an Electron Beam Ion Trap at energies of 2 to 3 keVu{sup -1}, charge-selected and directed onto targets comprising arrays of nanoscale apertures in silicon nitride membranes. The highly charged ions implemented are Ar{sup 16+} and Xe{sup 44+} and the aperture targets are formed by focused ion beam drilling in combination with ion beam assisted thin film deposition, achieving hole diameters of 50 to 300 nm and aspect ratios of 1:5 to 3:2. After transport through the nanoscale apertures the ions pass through an electrostatic charge state analyzer and are detected. The percentage of electron capture from the aperture walls is found to be much lower than model predictions and the results are discussed in terms of a capillary guiding mechanism. (orig.)

  15. Is ion channel selectivity mediated by confined water?

    CERN Document Server

    Prada-Gracia, Diego

    2012-01-01

    Ion channels form pores across the lipid bilayer, selectively allowing inorganic ions to cross the membrane down their electrochemical gradient. While the study of ion desolvation free-energies have attracted much attention, the role of water inside the pore is less clear. Here, molecular dynamics simulations of a reduced model of the KcsA selectivity filter indicate that the equilibrium position of Na+, but not of K+, is strongly influenced by confined water. The latter forms a stable complex with Na+, moving the equilibrium position of the ion to the plane of the backbone carbonyls. Almost at the centre of the binding site, the water molecule is trapped by favorable electrostatic interactions and backbone hydrogen-bonds. In the absence of confined water the equilibrium position of both Na+ and K+ is identical. Our observations strongly suggest a previously unnoticed active role of confined water in the selectivity mechanism of ion channels.

  16. Potentiometric determination of K + ions using a K + -selective ...

    African Journals Online (AJOL)

    This paper describes analytical applications of K+-selective liquid membrane electrode. The membrane is the solution of the active complex formed by the K+ ions with dibenzo-18-crown-6 ionophore (DB-[18]-C-6) extracted in propylenecarbonate (PC). Successful application of the developed electrode for K+ ions ...

  17. Bio-inspired ion selective crown-ether polymer membranes

    NARCIS (Netherlands)

    Tas, Sinem

    2016-01-01

    Development of unctional membranes that are capable of selectively recognizing and transporting ions have key importance for the recovery and separation of specific icons (e.d. K+, Li+, Na+) from multicomponent mixtures. In this thesis, new membrane materials based on crown ether-metal ion

  18. Development of a linear-type double reflectron for focused imaging of photofragment ions from mass-selected complex ions

    Science.gov (United States)

    Okutsu, Kenichi; Nakashima, Yuji; Yamazaki, Kenichiro; Fujimoto, Keita; Nakano, Motoyoshi; Ohshimo, Keijiro; Misaizu, Fuminori

    2017-05-01

    An ion imaging apparatus with a double linear reflectron mass spectrometer has been developed, in order to measure velocity and angular distributions of mass-analyzed fragment ions produced by photodissociation of mass-selected gas phase complex ions. The 1st and the 2nd linear reflectrons were placed facing each other and controlled by high-voltage pulses in order to perform the mass-separation of precursor ions in the 1st reflectron and to observe the focused image of the photofragment ions in the 2nd reflectron. For this purpose, metal meshes were attached on all electrodes in the 1st reflectron, whereas the mesh was attached only on the last electrode in the 2nd reflectron. The performance of this apparatus was evaluated using imaging measurement of Ca+ photofragment ions from photodissociation reaction of Ca+Ar complex ions at 355 nm photoexcitation. The focused ion images were obtained experimentally with the double linear reflectron at the voltages of the reflection electrodes close to the predictions by ion trajectory simulations. The velocity and angular distributions of the produced Ca+ ([Ar] 4p1, 2P3/2) ion were analyzed from the observed images. The binding energy D0 of Ca+Ar in the ground state deduced in the present measurement was consistent with those determined theoretically and by spectroscopic measurements. The anisotropy parameter β of the transition was evaluated for the first time by this instrument.

  19. Spectroscopy with trapped highly charged ions

    Energy Technology Data Exchange (ETDEWEB)

    Beiersdorfer, P

    2008-01-23

    We give an overview of atomic spectroscopy performed on electron beam ion traps at various locations throughout the world. Spectroscopy at these facilities contributes to various areas of science and engineering, including but not limited to basic atomic physics, astrophysics, extreme ultraviolet lithography, and the development of density and temperature diagnostics of fusion plasmas. These contributions are accomplished by generating, for example, spectral surveys, making precise radiative lifetime measurements, accounting for radiative power emitted in a given wavelength band, illucidating isotopic effects, and testing collisional-radiative models. While spectroscopy with electron beam ion traps had originally focused on the x-ray emission from highly charged ions interacting with the electron beam, the operating modes of such devices have expanded to study radiation in almost all wavelength bands from the visible to the hard x-ray region; and at several facilities the ions can be studied even in the absence of an electron beam. Photon emission after charge exchange or laser excitation has been observed, and the work is no longer restricted to highly charged ions. Much of the experimental capabilities are unique to electron beam ion traps, and the work performed with these devices cannot be undertaken elsewhere. However, in other areas the work on electron beam ion traps rivals the spectroscopy performed with conventional ion traps or heavy-ion storage rings. The examples we present highlight many of the capabilities of the existing electron beam ion traps and their contributions to physics.

  20. The ion adsorption effect on selectivity of liquid state, O,O'-didecylodithiophosphate chelate based ion-selective electrodes.

    Science.gov (United States)

    Ren, K

    2000-09-05

    Ion-selective electrodes with liquid membranes including O,O'-didecylo-dithiophosphate complexes of Tl(I), Pb(II), Cd(II) and Ni(II) are characterised and results of the study on their selectivity are reported. A short review of problems related to determination and interpretation of selectivity coefficients of ion-selective electrodes is presented with particular emphasis on the drawbacks of the hitherto used methods. A new method is proposed, which in the experimental part is close to that of mixed solutions recommended by IUPAC but can be applied also when the latter is of no use. The method proposed for determination of selectivity coefficients simultaneously allows concluding about the mechanism of potential generation. A few examples of relations between selectivity coefficients of the electrodes and concentrations of disturbing ions in solutions, are given. An interpretation of the above relations as results of the processes of ion adsorption at the interface of the electrode membrane and water solution is proposed. The results obtained have confirmed the hypothesis given by Pungor, according to which the main role in the mechanism of generation of ion-selective electrodes potential is played by the processes of ion chemisorption at the interface of the membrane and water solution.

  1. The effect of counter-ions on the ion selectivity of potassium and sodium ions in nanopores.

    Science.gov (United States)

    Tang, Dai; Kim, Daejoong

    2014-01-01

    The ion selective transport plays an important role in the function of cell membranes, and promotes the application of artificial permeable membranes. This phenomenon has been studied in case for different diameters and functional groups of nanopores. In this work, we focus on the effect of anions on cation selectivity, in particular the influence of various halide ions on K+ and Na+ selectivity. We adopted molecular dynamics simulations with non-charged nanopores under constant temperature and uniform concentration. The results show K+-selectivity in the solution with Cl- and Na+-selectivity in the solution with Br- and I-. This selectivity, on the contrary, disappears in the solution with F-. We also investigate the change of the hydration shell of ions and cation-anion interactions between in the bulk region and in the nanopores, which could explain this selective phenomenon.

  2. High Intensity High Charge State ECR Ion Sources

    CERN Document Server

    Leitner, Daniela

    2005-01-01

    The next-generation heavy ion beam accelerators such as the proposed Rare Isotope Accelerator (RIA), the Radioactive Ion Beam Factory at RIKEN, the GSI upgrade project, the LHC-upgrade, and IMP in Lanzhou require a great variety of high charge state ion beams with a magnitude higher beam intensity than currently achievable. High performance Electron Cyclotron Resonance (ECR) ion sources can provide the flexibility since they can routinely produce beams from hydrogen to uranium. Over the last three decades, ECR ion sources have continued improving the available ion beam intensities by increasing the magnetic fields and ECR heating frequencies to enhance the confinement and the plasma density. With advances in superconducting magnet technology, a new generation of high field superconducting sources is now emerging, designed to meet the requirements of these next generation accelerator projects. The talk will briefly review the field of high performance ECR ion sources and the latest developments for high intens...

  3. Cobalt bis(dicarbollide) ions with covalently bonded CMPO groups as selective extraction agents for lanthanide and actinide cations from highly acidic nuclear waste solutions

    Energy Technology Data Exchange (ETDEWEB)

    Gruner, B.; Plesek, J.; Baca, J. [Academy of Sciences of the Czech Republic, Institute of Inorganic Chemistry, Prague (Czech Republic); Cisarova, I. [Charles University, Dept. of Chemistry, Faculty of Natural Sciences, Prague (Czech Republic); Dozol, J.F.; Rouquette, H. [CEA Cadarache, Dept. d' Etudes des Dechets, DED/LCD, 13 - Saint Paul lez Durance (France); Vinas, C. [Institute of Material Sciences, CSIC, Bellaterra (Spain); Selucky, P.; Rais, J. [Nuclear Research Institute plc., Rez near Prague (Czech Republic)

    2002-10-01

    A new series of boron substituted cobalt bis(dicarbollide)(1-) ion (1) derivatives of the general formula [(8-CMPO-(CH{sub 2}-CH{sub 2}O){sub 2}-1,2-C{sub 2}B{sub 9}H{sub 10})(1',2'-C{sub 2}B{sub 9}H{sub 11})-3,3'-Co]{sup -} (CMPO = Ph{sub 2}P(O)-CH{sub 2}C(O)NR, R = C{sub 4}H{sub 9} (3b), -C{sub 12}H{sub 25} (4b), -CH{sub 2}-C{sub 6}H{sub 5} (5b)) was prepared by ring cleavage of the 8-dioxane-cobalt bis(dicarbollide) (2) bi-polar compound by the respective primary amines and by subsequent reaction of the resulting amino derivatives (3a-5a) with the nitrophenyl ester of diphenyl-phosphoryl-acetic acid. The compounds were synthesized with the aim to develop a new class of more efficient extraction agents for liquid/liquid extraction of polyvalent cations, i.e. lanthanides and actinides, from high-level activity nuclear waste. All compounds were characterized by a combination of {sup 11}B NMR, {sup 1}H high field NMR, Mass Spectrometry with Electro-spray and MALDI TOF ionisation, HPLC and other techniques. The molecular structure of the supramolecular Ln{sup 3+} complex of the anion 5b was determined by single crystal X-ray diffraction analysis. Crystallographic results proved that the Ln(m) atom is bonded to three functionalized cobalt bis(dicarbollide) anions in a charge compensated complex. The cation is tightly coordinated by six oxygen atoms of the CMPO terminal groups (two of each ligand) and by three water molecules completing the metal coordination number to 9. Atoms occupying the primary coordination sphere form a tri-capped trigonal prismatic arrangement. Very high liquid-liquid extraction efficiency of all anionic species was observed. Moreover, less polar toluene can be applied as an auxiliary solvent replacing the less environmentally friendly nitro- and chlorinated solvents used in the current dicarbollide liquid-liquid extraction process. The extraction coefficients are sufficiently high for possible technological applications. (authors)

  4. High Rate Performing Li-ion Battery

    Science.gov (United States)

    2015-02-09

    permeable to lithium ions and efficient in transferring the electrons into/from the LVP surface to the corresponding current collector. a) b) c) d) e...PO4)3/C for High Rate Lithium-ion Battery Applications”, Lee Hwang Sheng, Nail Suleimanov, Vishwanathan Ramar, Mangayarkarasi Murugan, Kuppan

  5. High Selectivity Oxygen Delignification

    Energy Technology Data Exchange (ETDEWEB)

    Lucian A. Lucia

    2005-11-15

    Project Objective: The objectives of this project are as follows: (1) Examine the physical and chemical characteristics of a partner mill pre- and post-oxygen delignified pulp and compare them to lab generated oxygen delignified pulps; (2) Apply the chemical selectivity enhancement system to the partner pre-oxygen delignified pulps under mill conditions (with and without any predetermined amounts of carryover) to determine how efficiently viscosity is preserved, how well selectivity is enhanced, if strength is improved, measure any yield differences and/or bleachability differences; and (3) Initiate a mill scale oxygen delignification run using the selectivity enhancement agent, collect the mill data, analyze it, and propose any future plans for implementation.

  6. Selective minority-ion heating in the afterglow of an electron cyclotron resonance ion source

    NARCIS (Netherlands)

    Nadzeyka, A; Meyer, D; Barzangy, F; Drentje, AG; Wiesemann, K

    We report first experimental results on selective minority-ion heating in the afterglow mode of electron cyclotron resonance ion sources in Bochum and at the KVI (Groningen) in mixtures of Ar/O/He and in pure nitrogen. In addition we measured time resolved vacuum ultraviolet-line intensities of

  7. Production of High-Intensity, Highly Charged Ions

    CERN Document Server

    Gammino, S.

    2013-12-16

    In the past three decades, the development of nuclear physics facilities for fundamental and applied science purposes has required an increasing current of multicharged ion beams. Multiple ionization implies the formation of dense and energetic plasmas, which, in turn, requires specific plasma trapping configurations. Two types of ion source have been able to produce very high charge states in a reliable and reproducible way: electron beam ion sources (EBIS) and electron cyclotron resonance ion sources (ECRIS). Multiple ionization is also obtained in laser-generated plasmas (laser ion sources (LIS)), where the high-energy electrons and the extremely high electron density allow step-by-step ionization, but the reproducibility is poor. This chapter discusses the atomic physics background at the basis of the production of highly charged ions and describes the scientific and technological features of the most advanced ion sources. Particular attention is paid to ECRIS and the latest developments, since they now r...

  8. 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.

  9. Photon-trap spectroscopy of mass-selected ions in an ion trap: optical absorption and magneto-optical effects.

    Science.gov (United States)

    Terasaki, Akira; Majima, Takuya; Kondow, Tamotsu

    2007-12-21

    A novel experimental technique has been developed to observe a trace of optical absorption of free mass-selected ions. The technique combines a linear radio-frequency ion trap with a high-finesse optical cavity to perform cavity ring-down spectroscopy (photon-trap spectroscopy for generality), where the storage lifetime of photons in the cavity provides a sensitivity high enough to probe the trapped ions. Absorption spectra of the manganese ion Mn(+) are presented, showing hyperfine structures for the (7)P(2,3,4)<--(7)S(3) transitions in the ultraviolet range. Implementation of a solenoidal magnet allows us to observe the Zeeman splitting and the Faraday rotation as well.

  10. High current pelletron for ion implantation

    Science.gov (United States)

    Schroeder, James B.

    1989-04-01

    Since 1984, when the first production MeV ion implanter (an NEC model MV-T30) went on-line, interest in versatile electrostatic accelerator systems for MeV ion implantation has grown. The systems use a negative ion source to inject a tandem megavolt accelerator. In early systems the 0.4 mA of charging current from the two Pelletron charging chains in the accelerator was sufficient for the low intensity of beams from the ion source. This 2-chain system, however, is no longer adequate for the much higher beam intensities from today's improved ion sources. A 4-chain charging system, which delivers 1.3 mA to the high voltage terminal, was developed and is in operation in new models of NEC S Series Pelletron accelerators. This paper describes the latest beam performance of 1 MV and 1.7 MV Pelletron accelerators with this new 4-chain charging system.

  11. High sensitivity field asymmetric ion mobility spectrometer.

    Science.gov (United States)

    Chavarria, Mario A; Matheoud, Alessandro V; Marmillod, Philippe; Liu, Youjiang; Kong, Deyi; Brugger, Jürgen; Boero, Giovanni

    2017-03-01

    A high sensitivity field asymmetric ion mobility spectrometer (FAIMS) was designed, fabricated, and tested. The main components of the system are a 10.6 eV UV photoionization source, an ion filter driven by a high voltage/high frequency n-MOS inverter circuit, and a low noise ion detector. The ion filter electronics are capable to generate square waveforms with peak-to-peak voltages up to 1000 V at frequencies up to 1 MHz with adjustable duty cycles. The ion detector current amplifier has a gain up to 10 12 V/A with an effective equivalent input noise level down to about 1 fA/Hz 1/2 during operation with the ion filter at the maximum voltage and frequency. The FAIMS system was characterized by detecting different standard chemical compounds. Additionally, we investigated the use of a synchronous modulation/demodulation technique to improve the signal-to-noise ratio in FAIMS measurements. In particular, we implemented the modulation of the compensation voltage with the synchronous demodulation of the ion current. The analysis of the measurements at low concentration levels led to an extrapolated limit of detection for acetone of 10 ppt with an averaging time of 1 s.

  12. High sensitivity field asymmetric ion mobility spectrometer

    Science.gov (United States)

    Chavarria, Mario A.; Matheoud, Alessandro V.; Marmillod, Philippe; Liu, Youjiang; Kong, Deyi; Brugger, Jürgen; Boero, Giovanni

    2017-03-01

    A high sensitivity field asymmetric ion mobility spectrometer (FAIMS) was designed, fabricated, and tested. The main components of the system are a 10.6 eV UV photoionization source, an ion filter driven by a high voltage/high frequency n-MOS inverter circuit, and a low noise ion detector. The ion filter electronics are capable to generate square waveforms with peak-to-peak voltages up to 1000 V at frequencies up to 1 MHz with adjustable duty cycles. The ion detector current amplifier has a gain up to 1012 V/A with an effective equivalent input noise level down to about 1 fA/Hz1/2 during operation with the ion filter at the maximum voltage and frequency. The FAIMS system was characterized by detecting different standard chemical compounds. Additionally, we investigated the use of a synchronous modulation/demodulation technique to improve the signal-to-noise ratio in FAIMS measurements. In particular, we implemented the modulation of the compensation voltage with the synchronous demodulation of the ion current. The analysis of the measurements at low concentration levels led to an extrapolated limit of detection for acetone of 10 ppt with an averaging time of 1 s.

  13. A high performance microfabricated surface ion trap

    Science.gov (United States)

    Lobser, Daniel; Blain, Matthew; Haltli, Raymond; Hollowell, Andrew; Revelle, Melissa; Stick, Daniel; Yale, Christopher; Maunz, Peter

    2017-04-01

    Microfabricated surface ion traps present a natural solution to the problem of scalability in trapped ion quantum computing architectures. We address some of the chief concerns about surface ion traps by demonstrating low heating rates, long trapping times as well as other high-performance features of Sandia's high optical access (HOA-2) trap. For example, due to the HOA's specific electrode layout, we are able to rotate principal axes of the trapping potential from 0 to 2 π without any change in the secular trap frequencies. We have also achieved the first single-qubit gates with a diamond norm below a rigorous fault tolerance threshold, and a two-qubit Mølmer-Sørensen gate with a process fidelity of 99.58(6). Here we present specific details of trap capabilities, such as shuttling and ion reordering, as well as details of our high fidelity single- and two-qubit gates.

  14. Convergent Evolution of Sodium Ion Selectivity in Metazoan Neuronal Signaling

    Directory of Open Access Journals (Sweden)

    Maya Gur Barzilai

    2012-08-01

    Full Text Available Ion selectivity of metazoan voltage-gated Na+ channels is critical for neuronal signaling and has long been attributed to a ring of four conserved amino acids that constitute the ion selectivity filter (SF at the channel pore. Yet, in addition to channels with a preference for Ca2+ ions, the expression and characterization of Na+ channel homologs from the sea anemone Nematostella vectensis, a member of the early-branching metazoan phylum Cnidaria, revealed a sodium-selective channel bearing a noncanonical SF. Mutagenesis and physiological assays suggest that pore elements additional to the SF determine the preference for Na+ in this channel. Phylogenetic analysis assigns the Nematostella Na+-selective channel to a channel group unique to Cnidaria, which diverged >540 million years ago from Ca2+-conducting Na+ channel homologs. The identification of Cnidarian Na+-selective ion channels distinct from the channels of bilaterian animals indicates that selectivity for Na+ in neuronal signaling emerged independently in these two animal lineages.

  15. High Selectivity Oxygen Delignification

    Energy Technology Data Exchange (ETDEWEB)

    Arthur J. Ragauskas

    2005-09-30

    The overall objective of this program was to develop improved extended oxygen delignification (EOD) technologies for current U.S. pulp mill operations. This was accomplished by: (1) Identifying pulping conditions that optimize O and OO performance; (2) Identifying structural features of lignin that enhance reactivity towards EOD of high kappa pulps; (3) Identifying factors minimizing carbohydrate degradation and improve pulp strength of EOD high kappa pulps; (4) Developing a simple, reproducible method of quantifying yield gains from EOD; and (5) Developing process conditions that significantly reduce the capital requirements of EOD while optimizing the yield benefits. Key research outcomes included, demonstrating the use of a mini-O sequence such as (E+O)Dkf:0.05(E+O) or Dkf:0.05(E+O)(E+O) without interstage washing could capture approximately 60% of the delignification efficiency of a conventional O-stage without the major capital requirements associated with an O-stage for conventional SW kraft pulps. The rate of formation and loss of fiber charge during an O-stage stage can be employed to maximize net fiber charge. Optimal fiber charge development and delignification are two independent parameters and do not parallel each other. It is possible to utilize an O-stage to enhance overall cellulosic fiber charge of low and high kappa SW kraft pulps which is beneficial for physical strength properties. The application of NIR and multi-variant analysis was developed into a rapid and simple method of determining the yield of pulp from an oxygen delignification stage that has real-world mill applications. A focus point of this program was the demonstration that Kraft pulping conditions and oxygen delignification of high and low-kappa SW and HW pulps are intimately related. Improved physical pulp properties and yield can be delivered by controlling the H-factor and active alkali charge. Low AA softwood kraft pulp with a kappa number 30 has an average improvement of 2% in

  16. Conducting ion tracks generated by charge-selected swift heavy ions

    Energy Technology Data Exchange (ETDEWEB)

    Gupta, Srashti, E-mail: srashti.3@gmail.com [II. Physikalisches Institut, Universität Göttingen, 37077 Göttingen (Germany); Department of Physics & Astrophysics, Delhi University, New Delhi, Delhi 110007 (India); Gehrke, H.G., E-mail: h.gehrke@fz-juelich.de [II. Physikalisches Institut, Universität Göttingen, 37077 Göttingen (Germany); Forschungszentrum Jülich, 52425 Jülich (Germany); Krauser, J., E-mail: jkrauser@hs-harz.de [Harz University of Applied Sciences, 38855 Wernigerode (Germany); Trautmann, C., E-mail: C.Trautmann@gsi.de [Helmholtzzentrum für Schwerionenforschung, 64291 Darmstadt (Germany); Technische Universität Darmstadt, Alarich-Weiss-Straße2, 64287 Darmstadt (Germany); Severin, D., E-mail: D.Severin@gsi.de [Helmholtzzentrum für Schwerionenforschung, 64291 Darmstadt (Germany); Bender, M., E-mail: M.Bender@gsi.de [Helmholtzzentrum für Schwerionenforschung, 64291 Darmstadt (Germany); Rothard, H., E-mail: rothard@ganil.fr [Centre de Recherche sur les Ions, les Materiaux et la Photonique, CIMAP-CIRIL-Ganil, F-14070 Caen (France); Hofsäss, H., E-mail: hans.hofsaess@phys.uni-goettingen.de [II. Physikalisches Institut, Universität Göttingen, 37077 Göttingen (Germany)

    2016-08-15

    Conducting ion tracks in tetrahedral amorphous carbon (ta-C) thin films were generated by irradiation with swift heavy ions of well-defined charge state. The conductivity of tracks and the surface topography of the films, showing characteristic hillocks at each track position, were investigated using conductive atomic force microscopy measurements. The dependence of track conductivity and hillock size on the charge state of the ions was studied using 4.6 MeV/u Pb ions of charge state 53+, 56+ and 60+ provided by GANIL, as well as 4.8 MeV/u Bi and Au ions of charge state from 50+ to 61+ and 4.2 MeV/u {sup 238}U ions in equilibrium charge state provided by UNILAC of GSI. For the charge state selection at GSI, an additional stripper-foil system was installed at the M-branch that now allows routine irradiations with ions of selected charge states. The conductivity of tracks in ta-C increases significantly when the charge state increases from 51+ to 60+. However, the conductivity of individual tracks on the same sample still shows large variations, indicating that tracks formed in ta-C are either inhomogeneous or the conductivity is limited by the interface between ion track and Si substrate.

  17. Click synthesis of podand triazole-linked gold nanoparticles as highly selective and sensitive colorimetric probes for lead(II) ions.

    Science.gov (United States)

    Li, Haibing; Zheng, Qiuling; Han, Cuiping

    2010-06-01

    Podand triazole-linked gold nanoparticles were designed via an in situ'click' reaction. The resulting gold nanoparticles were characterized by UV-vis spectroscopy, FT-IR spectroscopy, transmission electron microscopy (TEM). Podand triazole-linked gold nanoparticles were utilized as colorimetric probes for Pb(2+)via Pb(2+)-induced gold nanoparticle aggregation which incorporates two podand molecules from different nanoparticles forming an intermolecule type of association. Moreover, the application of the resulting gold nanoparticles to evaluate the exceeding standard of lead ions in drinking water and leaded paint was investigated.

  18. Self-terminated etching of GaN with a high selectivity over AlGaN under inductively coupled Cl2/N2/O2 plasma with a low-energy ion bombardment

    Science.gov (United States)

    Zhong, Yaozong; Zhou, Yu; Gao, Hongwei; Dai, Shujun; He, Junlei; Feng, Meixin; Sun, Qian; Zhang, Jijun; Zhao, Yanfei; DingSun, An; Yang, Hui

    2017-10-01

    Etching of GaN/AlGaN heterostructure by O-containing inductively coupled Cl2/N2 plasma with a low-energy ion bombardment can be self-terminated at the surface of the AlGaN layer. The estimated etching rates of GaN and AlGaN were 42 and 0.6 nm/min, respectively, giving a selective etching ratio of 70:1. To study the mechanism of the etching self-termination, detailed characterization and analyses were carried out, including X-ray photoelectron spectroscopy (XPS) and time-of-flight secondary ion mass spectroscopy (TOF-SIMS). It was found that in the presence of oxygen, the top surface of the AlGaN layer was converted into a thin film of (Al,Ga)Ox with a high bonding energy, which effectively prevented the underlying atoms from a further etching, resulting in a nearly self-terminated etching. This technique enables a uniform and reproducible fabrication process for enhancement-mode high electron mobility transistors with a p-GaN gate.

  19. Pyrrole-coupled salicylimine-based fluorescence "turn on" probe for highly selective recognition of Zn²⁺ ions in mixed aqueous media: Application in living cell imaging.

    Science.gov (United States)

    Bhosale, Jitendra; Fegade, Umesh; Bondhopadhyay, Banashree; Kaur, Simanpreet; Singh, Narinder; Basu, Anupam; Dabur, Rajesh; Bendre, Ratnamala; Kuwar, Anil

    2015-06-01

    Cation sensing behaviour of a pyrrole-based derivative (2-hydroxyl 3 methyl 6 isopropyl benzaldehyde}-3,4-dimethyl-1H-pyrrole-2-carbohydrazide (receptor 3) has been explored and is found to be selective towards Zn(2+) over a variety of tested cations. The receptor 3 has shown high selectivity and sensitivity towards Zn(2+) over the other alkali, alkaline earth and transition metal ions. In the presence of Zn(2+), absorption band of receptor 3 has shown the red shift. The sensing behaviour has been suggested to continue via enhancement process which has further been supported by UV-vis absorption and theoretical density functional theory (DFT) calculations indicating the formation of a 1:1 complex between the pyrrole based receptor 3 and Zn(2+). The present work is presenting a highly selective dual channel colorimetric sensor for zinc with great sensitivity. The developed sensor was successfully applied to image intracellular Zn(2+) in living cells. Copyright © 2015 John Wiley & Sons, Ltd.

  20. Thermal responsive ion selectivity of uranyl peroxide nanocages. An inorganic mimic of K{sup +} ion channels

    Energy Technology Data Exchange (ETDEWEB)

    Gao, Yunyi; Sun, Xinyu; Liu, Tianbo [Akron Univ., OH (United States). Dept. of Polymer Science; Szymanowski, Jennifer E.S.; Burns, Peter C. [Notre Dame Univ., IN (United States). Dept. of Civil Engineering and Geological Sciences

    2016-06-06

    An actinyl peroxide cage cluster, Li{sub 48+m}K{sub 12}(OH){sub m}[UO{sub 2}(O{sub 2})(OH)]{sub 60} (H{sub 2}O){sub n} (m∼20 and n∼310; U{sub 60}), discriminates precisely between Na{sup +} and K{sup +} ions when heated to certain temperatures, a most essential feature for K{sup +} selective filters. The U{sub 60} clusters demonstrate several other features in common with K{sup +} ion channels, including passive transport of K{sup +} ions, a high flux rate, and the dehydration of U{sub 60} and K{sup +} ions. These qualities make U{sub 60} (a pure inorganic cluster) a promising ion channel mimic in an aqueous environment. Laser light scattering (LLS) and isothermal titration calorimetry (ITC) studies revealed that the tailorable ion selectivity of U{sub 60} clusters is a result of the thermal responsiveness of the U{sub 60} hydration shells.

  1. Thermal responsive ion selectivity of uranyl peroxide nanocages: an inorganic mimic of K{sup +} ion channels

    Energy Technology Data Exchange (ETDEWEB)

    Gao, Yunyi; Sun, Xinyu; Liu, Tianbo [Department of Polymer Science, University of Akron, Akron, OH (United States); Szymanowski, Jennifer E.S.; Burns, Peter C. [Department of Civil Engineering and Geological Sciences, University of Notre Dame, Notre Dame, IN (United States)

    2016-06-06

    An actinyl peroxide cage cluster, Li{sub 48+m}K{sub 12}(OH){sub m}[UO{sub 2}(O{sub 2})(OH)]{sub 60} (H{sub 2}O){sub n} (m∼20 and n∼310; U{sub 60}), discriminates precisely between Na{sup +} and K{sup +} ions when heated to certain temperatures, a most essential feature for K{sup +} selective filters. The U{sub 60} clusters demonstrate several other features in common with K{sup +} ion channels, including passive transport of K{sup +} ions, a high flux rate, and the dehydration of U{sub 60} and K{sup +} ions. These qualities make U{sub 60} (a pure inorganic cluster) a promising ion channel mimic in an aqueous environment. Laser light scattering (LLS) and isothermal titration calorimetry (ITC) studies revealed that the tailorable ion selectivity of U{sub 60} clusters is a result of the thermal responsiveness of the U{sub 60} hydration shells. (copyright 2016 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  2. Three luminescent d{sup 10} metal coordination polymers assembled from a semirigid V-shaped ligand with high selective detecting of Cu{sup 2+} ion and nitrobenzene

    Energy Technology Data Exchange (ETDEWEB)

    Wu, Wei-Ping [Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of the Ministry of Education, Shaanxi Key Laboratory of Physico-Inorg. Chem., College of Chemistry & Materials Science, Northwest University, Xi’an 710069 (China); Institute of Functional Materials, College of Chemistry and Pharmaceutical Engineering, Sichuan University of Science & Engineering, Zigong 643000 (China); Liu, Ping; Liang, Yu-Tong; Cui, Lin; Xi, Zheng-Ping [Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of the Ministry of Education, Shaanxi Key Laboratory of Physico-Inorg. Chem., College of Chemistry & Materials Science, Northwest University, Xi’an 710069 (China); Wang, Yao-Yu, E-mail: wyaoyu@nwu.edu.cn [Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of the Ministry of Education, Shaanxi Key Laboratory of Physico-Inorg. Chem., College of Chemistry & Materials Science, Northwest University, Xi’an 710069 (China)

    2015-08-15

    Three 2D luminescent coordination polymers with helical frameworks, [ZnL{sub 2}]{sub n} (1) and ([ML{sub 2}]·(H{sub 2}O)){sub n} (M=Zn (2), Cd (3)) (HL=4-((2-methyl-1 H-imidazol-1-yl)methyl)benzoic acid), have been assembled under hydro(solvo)thermal conditions. Complex 1 is in chiral space group and displays a rare 2D→2D 2-fold parallel interpenetrated layer network with two types of chiral double helixes. Interestingly, the single crystal structure analyses indicate the coexistence of enantiomers la and 1b in one pot, while the bulk crystallization of 1 are racemic mixtures based on the CD measurement. 2 and 3 are isostructural, in the structure, there are two kinds of 2D chiral helical-layers which stack in an -ABAB- sequence leading to the overall structure are mesomer and achiral. All compounds display intense luminescence in solid state at room temperature with high chemical and thermal stability. More importantly, 1 has been successfully applied in the detection of Cu{sup 2+} ions in aqueous media and nitrobenzene and the probable detecting mechanism was also discussed. - Graphical abstract: Three luminescent d{sup 10} metal coordination polymers with helical-layer based on 4-((2-methyl-1H-imidazol-1-yl)methyl)benzoic acid have been obtained. Compound 1 shows high selective detecting for Cu{sup 2+} ion in aqueous and nitrobenzene. - Highlights: • Three coordination polymers with chiral helical-layer have been obtained. • 1 Can luminescent detect Cu{sup 2+} ion in aqueous media and nitrobenzene. • Racemic mixture or mesomer compounds can be obtained by controlling the reaction conditions.

  3. Ion-selective electrodes: historical, mechanism of response, selectivity and concept review

    Directory of Open Access Journals (Sweden)

    Fernandes Julio Cesar Bastos

    2001-01-01

    Full Text Available This paper presents a review of the concepts involved in the working mechanism of the ion-selective electrodes, searching a historical overview, moreover to describe the new advances in the area.

  4. Coulomb crystallization of highly charged ions.

    Science.gov (United States)

    Schmöger, L; Versolato, O O; Schwarz, M; Kohnen, M; Windberger, A; Piest, B; Feuchtenbeiner, S; Pedregosa-Gutierrez, J; Leopold, T; Micke, P; Hansen, A K; Baumann, T M; Drewsen, M; Ullrich, J; Schmidt, P O; López-Urrutia, J R Crespo

    2015-03-13

    Control over the motional degrees of freedom of atoms, ions, and molecules in a field-free environment enables unrivalled measurement accuracies but has yet to be applied to highly charged ions (HCIs), which are of particular interest to future atomic clock designs and searches for physics beyond the Standard Model. Here, we report on the Coulomb crystallization of HCIs (specifically (40)Ar(13+)) produced in an electron beam ion trap and retrapped in a cryogenic linear radiofrequency trap by means of sympathetic motional cooling through Coulomb interaction with a directly laser-cooled ensemble of Be(+) ions. We also demonstrate cooling of a single Ar(13+) ion by a single Be(+) ion-the prerequisite for quantum logic spectroscopy with a potential 10(-19) accuracy level. Achieving a seven-orders-of-magnitude decrease in HCI temperature starting at megakelvin down to the millikelvin range removes the major obstacle for HCI investigation with high-precision laser spectroscopy. Copyright © 2015, American Association for the Advancement of Science.

  5. Ion imprinted polymeric nanoparticles for selective separation and sensitive determination of zinc ions in different matrices.

    Science.gov (United States)

    Shamsipur, Mojtaba; Rajabi, Hamid Reza; Pourmortazavi, Seied Mahdi; Roushani, Mahmoud

    2014-01-03

    Preparation of Zn(2+) ion-imprinted polymer (Zn-IIP) nanoparticles is presented in this report. The Zn-IIP nanoparticles are prepared by dissolving stoichiometric amounts of zinc nitrate and selected chelating ligand, 3,5,7,20,40-pentahydroxyflavone, in 15 mL ethanol-acetonitrile (2:1; v/v) mixture as a porogen solvent in the presence of ethylene glycol-dimethacrylate (EGDMA) as cross-linking, methacrylic acid (MAA) as functional monomer, and 2,2-azobisisobutyronitrile (AIBN) as initiator. After polymerization, Cavities in the polymer particles corresponding to the Zn(2+) ions were created by leaching the polymer in HCl aqueous solution. The synthesized IIPs were characterized by scanning electron microscopy, X-ray diffraction, Fourier transform infrared spectroscopy, fluorescence spectroscopy and thermal analysis techniques. Also, the pH range for rebinding of Zn(2+) ion on the IIP and equilibrium binding time were optimized, using flame atomic absorption spectrometry. In selectivity study, it was found that imprinting results increased affinity of the material toward Zn(2+) ion over other competitor metal ions with the same charge and close ionic radius. The prepared IIPs were repeatedly used and regenerated for six times without any significant decrease in polymer binding affinities. Finally, the prepared sorbent was successfully applied to the selective recognition and determination of zinc ion in different real samples. Copyright © 2013 Elsevier B.V. All rights reserved.

  6. Wavelength-selective fluorescence in ion channels formed by ...

    Indian Academy of Sciences (India)

    TECS

    Wavelength-selective fluorescence in ion channels formed by gramicidin A in membranes. AMITABHA CHATTOPADHYAY* and SATINDER S RAWAT. #. Centre for Cellular and Molecular Biology, Uppal Road, Hyderabad 500 007. #. Present address: 364 Plantation Street, Room 570R, Lazare Research Building,.

  7. Ionophores in polymeric membranes for selective ion recognition; impedance studies

    Energy Technology Data Exchange (ETDEWEB)

    Lisowska-Oleksiak, A. [Department of Chemical Technology, Gdansk University of Technology, ul. Narutowicza 11/12, 80-952 Gdansk (Poland)]. E-mail: alo@chem.pg.gda.pl; Lesinska, U. [Department of Chemical Technology, Gdansk University of Technology, ul. Narutowicza 11/12, 80-952 Gdansk (Poland); Nowak, A.P. [Department of Chemical Technology, Gdansk University of Technology, ul. Narutowicza 11/12, 80-952 Gdansk (Poland); Bochenska, M. [Department of Chemical Technology, Gdansk University of Technology, ul. Narutowicza 11/12, 80-952 Gdansk (Poland)]. E-mail: marboch@chem.pg.gda.pl

    2006-02-15

    Synthetic calix[4]arene-crown ionophores for selective Na{sup +} (ionophore L1) and Cs{sup +}-ions (ionophore L2) recognition find application in ion-selective membrane electrodes (ISE) for analytical purpose. Selectivity coefficients for the electrodes with compounds L1 and L2 are logK{sub Na,Cs}{sup pot}=-2.6 and logK{sub Cs,Na}{sup pot}=-2.4, respectively. Electrodes of two different construction: all-solid-state (ASS) (with conducting polymer layer on glassy carbon or platinum as ion-to-electron transducer) and conventional ion-selective electrode (ISE) (with liquid electrolyte and Ag/AgCl) are presented and their properties and lifetime are being compared. Resistance of PVC membrane with ionophores L1 and L2 were within the range 0.15-1.4M{omega} depending on the type of the outer electrolyte and its concentration. Conductivity of the membranes was in the range 0.7x10{sup -8} to 6x10{sup -8}{omega}{sup -1}cm{sup -1}. Warburg coefficients {sigma} were within 0.16x10{sup 4} to 12.7x10{sup 4}{omega}s{sup -1/2}, dielectric constant values {epsilon} were in a range 28-60 depending mainly on the type of plasticizer.

  8. Highly fluorescent nitrogen-doped carbon dots derived from Phyllanthus acidus utilized as a fluorescent probe for label-free selective detection of Fe3+ions, live cell imaging and fluorescent ink.

    Science.gov (United States)

    Atchudan, Raji; Edison, Thomas Nesakumar Jebakumar Immanuel; Aseer, Kanikkai Raja; Perumal, Suguna; Karthik, Namachivayam; Lee, Yong Rok

    2018-01-15

    A facile, economical and one-step hydrothermal method is used to synthesize highly durable fluorescent nitrogen-doped carbon dots (FNCDs) by utilizing Phyllanthus acidus (P. acidus) and aqueous ammonia as the carbon and nitrogen sources, respectively. The synthesized FNCDs have an average size of 4.5±1nm and showed bright blue fluorescence under the irradiation of UV-light at an excitation wavelength of 365nm. It exhibits a quantum yield (QY) of 14% at an excitation wavelength of 350nm with maximum emission at 420nm. X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared (FTIR) spectroscopy characterizations clearly showed the formation of FNCDs that predominantly consists of nitrogen and hydroxyl groups which can provide more adsorption sites. In addition, the above study reveals the successful bonding of nitrogen with carbon (C-N) in the FNCDs. The synthesized FNCDs with high QY can be used as efficient fluorescent probes for the detection of Fe 3+ . Based on the linear relationship between normalized fluorescence intensity and concentration of Fe 3+ ions, the prepared FNCDs can be used for label-free sensitive and selective detection of Fe 3+ ions in a wide concentration range of 2-25μM with a detection limit of 0.9μM. The present study proves that synthesized FNCDs has durable fluorescence, soluble in water very well and thus act as a promising candidate for the diverse applications such as label-free sensitive and selective detection of Fe 3+ , fluorescent ink and cellular imaging with good biocompatibility and low cytotoxicity. Copyright © 2017 Elsevier B.V. All rights reserved.

  9. Nanomolar determination of Pb (II ions by selective templated electrode

    Directory of Open Access Journals (Sweden)

    Mazloum-Ardakani Mohammad

    2012-01-01

    Full Text Available Polypyrrole modified electrode, prepared by electropolymerization of pyrrole in the presence of methyl red as a dopant, was templated with respect to Pb2+ ion and applied for potentiometric and voltammetric detection of this ion. The templating process improved the analytical response characteristics of the electrode, specially their selectivity, with respect to Pb2+ ion. The improvement depends on both the incorporated ligand (dopant and the templating process, with the latter being more vital. The potentiometric response of the electrode was linear within the Pb2+ concentration range of 2.0×10-6 to 5.0×10-2 M with a near-Nernstian slope of 28.6 mV decade-1 and a detection limit of 7.0 ×10-7 M. The electrode was also used for preconcentration differential pulse anodic stripping voltammetry (DPASV and results showed that peak currents for the incorporated lead species were dependent on the metal ion concentration in the range of 1.0×10-8 to 1.0×10-3 M. The detection limit of DPASV method was 3.5 ×10-9 M. The selectivity of the electrode with respect to some transition metal ions was investigated. The modified-templated electrode was used for the successful assay of lead in two standard reference material samples.

  10. Physical mechanisms leading to high currents of highly charged ions in laser-driven ion sources

    Energy Technology Data Exchange (ETDEWEB)

    Haseroth, Helmut [European Organization for Nuclear Research, Geneva (Switzerland); Hora, Heinrich [New South Wales Univ., Kensington, NSW (Australia)]|[Regensburg Inst. of Tech. (Germany). Anwenderzentrum

    1996-12-31

    Heavy ion sources for the big accelerators, for example, the LHC, require considerably more ions per pulse during a short time than the best developed classical ion source, the electron cyclotron resonance (ECR) provides; thus an alternative ion source is needed. This can be expected from laser-produced plasmas, where dramatically new types of ion generation have been observed. Experiments with rather modest lasers have confirmed operation with one million pulses of 1 Hz, and 10{sup 11} C{sup 4+} ions per pulse reached 2 GeV/u in the Dubna synchrotron. We review here the complexities of laser-plasma interactions to underline the unique and extraordinary possibilities that the laser ion source offers. The complexities are elaborated with respect to keV and MeV ion generation, nonlinear (ponderomotive) forces, self-focusing, resonances and ``hot`` electrons, parametric instabilities, double-layer effects, and the few ps stochastic pulsation (stuttering). Recent experiments with the laser ion source have been analyzed to distinguish between the ps and ns interaction, and it was discovered that one mechanism of highly charged ion generation is the electron impact ionization (EII) mechanism, similar to the ECR, but with so much higher plasma densities that the required very large number of ions per pulse are produced. (author).

  11. Nitrate Ion Selective Electrode Based on Ion Imprinted Poly(N-methylpyrrole

    Directory of Open Access Journals (Sweden)

    Ellen M. Bomar

    2017-01-01

    Full Text Available A poly(N-methylpyrrole based ion selective electrode (ISE has been prepared by electro-polymerization of N-methylpyrrole using potassium nitrate as the supporting electrolyte. Electrochemical and chemical variables were used to optimize the potentiometric response of the electrodes and to maximize the selectivity for nitrate over potential interferences. The selectivity, longevity and stability of the ion-imprinted polymer give this electrode advantages over traditional nitrate ISEs. The best prototype electrode exhibits a linear potential response to nitrate ion within the concentration range of 5.0 × 10−6 to 0.1 M nitrate with a near Nernstian slope of −56.3 mV per decade (R2 = 0.9998 and a strong preference for the nitrate ion over other anions. The selectivity coefficients of the electrode were evaluated by the fixed interference method. The use of N-methylpyrrole has advantages over pyrrole in terms of selectivity and pH insensitivity.

  12. Radioactive decays of highly-charged ions

    Directory of Open Access Journals (Sweden)

    Gao B. S.

    2015-01-01

    Full Text Available Access to stored and cooled highly-charged radionuclides offers unprecedented opportunities to perform high-precision investigations of their decays. Since the few-electron ions, e.g. hydrogen- or helium-like ions, are quantum mechanical systems with clear electronic ground state configurations, the decay studies of such ions are performed under well-defined conditions and allow for addressing fundamental aspects of the decay process. Presented here is a compact review of the relevant experiments conducted at the Experimental Storage Ring ESR of GSI. A particular emphasis is given to the investigations of the two-body beta decay, namely the bound-state β-decay and its time-mirrored counterpart, orbital electron-capture.

  13. Beam dynamics of mixed high intensity highly charged ion Beams in the Q/A selector

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, X.H., E-mail: zhangxiaohu@impcas.ac.cn [Institute of Modern Physics, Chinese Academy of Sciences, Lanzhou 730000 (China); Yuan, Y.J.; Yin, X.J.; Qian, C.; Sun, L.T. [Institute of Modern Physics, Chinese Academy of Sciences, Lanzhou 730000 (China); Du, H.; Li, Z.S.; Qiao, J.; Wang, K.D. [Institute of Modern Physics, Chinese Academy of Sciences, Lanzhou 730000 (China); University of Chinese Academy of Sciences, Beijing 100049 (China); Zhao, H.W.; Xia, J.W. [Institute of Modern Physics, Chinese Academy of Sciences, Lanzhou 730000 (China)

    2017-06-11

    Electron cyclotron resonance (ECR) ion sources are widely used in heavy ion accelerators for their advantages in producing high quality intense beams of highly charged ions. However, it exists challenges in the design of the Q/A selection systems for mixed high intensity ion beams to reach sufficient Q/A resolution while controlling the beam emittance growth. Moreover, as the emittance of beam from ECR ion sources is coupled, the matching of phase space to post accelerator, for a wide range of ion beam species with different intensities, should be carefully studied. In this paper, the simulation and experimental results of the Q/A selection system at the LECR4 platform are shown. The formation of hollow cross section heavy ion beam at the end of the Q/A selector is revealed. A reasonable interpretation has been proposed, a modified design of the Q/A selection system has been committed for HIRFL-SSC linac injector. The features of the new design including beam simulations and experiment results are also presented.

  14. Beam dynamics of mixed high intensity highly charged ion Beams in the Q/A selector

    Science.gov (United States)

    Zhang, X. H.; Yuan, Y. J.; Yin, X. J.; Qian, C.; Sun, L. T.; Du, H.; Li, Z. S.; Qiao, J.; Wang, K. D.; Zhao, H. W.; Xia, J. W.

    2017-06-01

    Electron cyclotron resonance (ECR) ion sources are widely used in heavy ion accelerators for their advantages in producing high quality intense beams of highly charged ions. However, it exists challenges in the design of the Q/A selection systems for mixed high intensity ion beams to reach sufficient Q/A resolution while controlling the beam emittance growth. Moreover, as the emittance of beam from ECR ion sources is coupled, the matching of phase space to post accelerator, for a wide range of ion beam species with different intensities, should be carefully studied. In this paper, the simulation and experimental results of the Q/A selection system at the LECR4 platform are shown. The formation of hollow cross section heavy ion beam at the end of the Q/A selector is revealed. A reasonable interpretation has been proposed, a modified design of the Q/A selection system has been committed for HIRFL-SSC linac injector. The features of the new design including beam simulations and experiment results are also presented.

  15. 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

  16. A Selective Iodide Ion Sensor Electrode Based on Functionalized ZnO Nanotubes

    Directory of Open Access Journals (Sweden)

    Magnus Willander

    2013-02-01

    Full Text Available In this research work, ZnO nanotubes were fabricated on a gold coated glass substrate through chemical etching by the aqueous chemical growth method. For the first time a nanostructure-based iodide ion selective electrode was developed. The ZnO nanotubes were functionalized with miconazole ion exchanger and the electromotive force (EMF was measured by the potentiometric method. The iodide ion sensor exhibited a linear response over a wide range of concentrations (1 × 10−6 to 1 × 10−1 M and excellent sensitivity of –62 ± 1 mV/decade. The detection limit of the proposed sensor was found to be 5 × 10−7 M. The effects of pH, temperature, additive, plasticizer and stabilizer on the potential response of iodide ion selective electrode were also studied. The proposed iodide ion sensor demonstrated a fast response time of less than 5 s and high selectivity against common organic and the inorganic anions. All the obtained results revealed that the iodide ion sensor based on functionalized ZnO nanotubes may be used for the detection of iodide ion in environmental water samples, pharmaceutical products and other real samples.

  17. A selective iodide ion sensor electrode based on functionalized ZnO nanotubes.

    Science.gov (United States)

    Ibupoto, Zafar Hussain; Khun, Kimleang; Willander, Magnus

    2013-02-04

    In this research work, ZnO nanotubes were fabricated on a gold coated glass substrate through chemical etching by the aqueous chemical growth method. For the first time a nanostructure-based iodide ion selective electrode was developed. The ZnO nanotubes were functionalized with miconazole ion exchanger and the electromotive force (EMF) was measured by the potentiometric method. The iodide ion sensor exhibited a linear response over a wide range of concentrations (1 × 10-6 to 1 × 10-1 M) and excellent sensitivity of -62 ± 1 mV/decade. The detection limit of the proposed sensor was found to be 5 × 10-7 M. The effects of pH, temperature, additive, plasticizer and stabilizer on the potential response of iodide ion selective electrode were also studied. The proposed iodide ion sensor demonstrated a fast response time of less than 5 s and high selectivity against common organic and the inorganic anions. All the obtained results revealed that the iodide ion sensor based on functionalized ZnO nanotubes may be used for the detection of iodide ion in environmental water samples, pharmaceutical products and other real samples.

  18. Metastable states of highly excited heavy ions

    Science.gov (United States)

    Pegg, D. J.; Griffin, P. M.; Sellin, I. A.; Smith, W. W.; Donnally, B.

    1973-01-01

    Description of the method used and results obtained in an experimental study of the metastable states of highly stripped heavy ions, aimed at determining the lifetimes of such states by the rates of autoionization and radiation. The significance and limitations of the results presented are discussed.

  19. BILAYER LIPID MEMBRANE (BLM) BASED ION SELECTIVE ELECTRODES AT THE MESO, MICRO, AND NANO SCALES

    Science.gov (United States)

    Liu, Bingwen; Rieck, Daniel; Van Wie, Bernard J.; Cheng, Gary J.; Moffett, David F.; Kidwell, David A.

    2009-01-01

    This paper presents a novel method for making micron-sized apertures with tapered sidewalls and nano-sized apertures. Their use in bilayer lipid membrane-based ion selective electrode design is demonstrated and compared to mesoscale bilayers and traditional PVC ion selective electrodes. Micron-sized apertures are fabricated in SU-8 photoresist films and vary in diameter from 10 to 40 microns. The tapered edges in SU-8 films are desired to enhance bilayer lipid membrane (BLM) formation and are fabricated by UV-light overexposure. Nanoapertures are made in boron diffused silicon film. The membranes are used as septa to separate two potassium chloride solutions of different concentrations. Lecithin BLMs are assembled on the apertures by ejecting lipid solution. Potassium ionophore, dibenzo-18-crown-6, is incorporated into BLMs by dissolving it in the lipid solution before membrane assembly. Voltage changes with increasing potassium ion concentrations are recorded with an A/D converter. Various ionophore concentrations in BLMs are investigated. At least a 1% concentration is needed for consistent slopes. Electrode response curves are linear over the 10−6 to 0.1 M range with a sub-Nernstian slope of 20 mV per Log concentration change. This system shows high selectivity to potassium ions over potential interfering sodium ions. BLMs on the three different aperture sizes at the meso, micro, and nano-scales all show similar linear ranges and limits of detection (LODs) as PVC ion selective membranes. PMID:19008091

  20. Application of electrochemically reduced graphene oxide on screen-printed ion-selective electrode.

    Science.gov (United States)

    Ping, Jianfeng; Wang, Yixian; Ying, Yibin; Wu, Jian

    2012-04-03

    In this study, a novel disposable all-solid-state ion-selective electrode using graphene as the ion-to-electron transducer was developed. The graphene film was prepared on screen-printed electrode directly from the graphene oxide dispersion by a one-step electrodeposition technique. Cyclic voltammetry and electrochemical impedance spectroscopy were employed to demonstrate the large double layer capacitance and fast charge transfer of the graphene film modified electrode. On the basis of these excellent properties, an all-solid-state calcium ion-selective electrode as the model was constructed using the calcium ion-selective membrane and graphene film modified electrode. The mechanism about the graphene promoting the ion-to-electron transformation was investigated in detail. The disposable electrode exhibited a Nernstian slope (29.1 mV/decade), low detection limit (10(-5.8) M), and fast response time (less than 10 s). With the high hydrophobic character of graphene materials, no water film was formed between the ion-selective membrane and the underlying graphene layer. Further studies revealed that the developed electrode was insensitive to light, oxygen, and redox species. The use of the disposable electrode for real sample analysis obtained satisfactory results, which made it a promising alternative in routine sensing applications.

  1. Solid-phase synthesis of highly fluorescent nitrogen-doped carbon dots for sensitive and selective probing ferric ions in living cells.

    Science.gov (United States)

    Zhang, Haijuan; Chen, Yonglei; Liang, Meijuan; Xu, Laifang; Qi, Shengda; Chen, Hongli; Chen, Xingguo

    2014-10-07

    Carbon quantum dots (C-Dots) have drawn extensive attention in recent years due to their stable physicochemical and photochemical properties. However, the development of nitrogen-doped carbon quantum dots (N-doped C-Dots) is still on its early stage. In this paper, a facile and high-output solid-phase synthesis approach was proposed for the fabrication of N-doped, highly fluorescent carbon quantum dots. The obtained N-doped C-Dots exhibited a strong blue emission with an absolute quantum yield (QY) of up to 31%, owing to fluorescence enhancement effect of introduced N atoms into carbon dots. The strong coordination of oxygen-rich groups on N-doped C-Dots to Fe(3+) caused fluorescence quenching via nonradiative electron-transfer, leading to the quantitative detection of Fe(3+). The probe exhibited a wide linear response concentration range (0.01-500 μM) to Fe(3+) with a detection limit of 2.5 nM. Significantly, the N-doped C-Dots possess negligible cytotoxicity, excellent biocompatibility, and high photostability. All these features are favorable for label-free monitoring of Fe(3+) in complex biological samples. It was then successfully applied for the fluorescence imaging of intracellular Fe(3+). As an efficient chemosensor, the N-doped C-Dots hold great promise to broaden applications in biological systems.

  2. Direct ion speciation analysis with ion-selective membranes operated in a sequential potentiometric/time resolved chronopotentiometric sensing mode.

    Science.gov (United States)

    Ghahraman Afshar, Majid; Crespo, Gastón A; Bakker, Eric

    2012-10-16

    Ion-selective membranes based on porous polypropylene membranes doped with an ionophore and a lipophilic cation-exchanger are used here in a new tandem measurement mode that combines dynamic electrochemistry and zero current potentiometry into a single protocol. Open circuit potential measurements yield near-nernstian response slopes in complete analogy to established ion-selective electrode methodology. Such measurements are well established to give direct information on the so-called free ion concentration (strictly, activity) in the sample. The same membrane is here also operated in a constant current mode, in which the localized ion depletion at a transition time is visualized by chronopotentiometry. This dynamic electrochemistry methodology gives information on the labile ion concentration in the sample. The sequential protocol is established on potassium and calcium ion-selective membranes. An increase of the ionophore concentration in the membrane to 180 mM makes it possible to determine calcium concentrations as high as 3 mM by chronopotentiometry, thereby making it possible to directly detect total calcium in undiluted blood samples. Recovery times after current perturbation depend on the current amplitude but can be kept to below 1 min for the polypropylene based ion-selective membranes studied here. Plasticized PVC as membrane material is less suited for this protocol, especially when the measurement at elevated concentrations is desired. An analysis of current amplitudes, transition times, and concentrations shows that the data are described by the Sand equation and that migration effects are insignificant. A numerical model describes the experimental findings with good agreement and gives guidance on the required selectivity in order to observe a well-resolved transition time and on the expected errors due to insufficient selectivity. The simulations suggest that the methodology compares well to that of open circuit potentiometry, despite giving

  3. Highly Charged Ions in Rare Earth Permanent Magnet Penning Traps

    CERN Document Server

    Guise, Nicholas D; Tan, Joseph N

    2013-01-01

    A newly constructed apparatus at the National Institute of Standards and Technology (NIST) is designed for the isolation, manipulation, and study of highly charged ions. Highly charged ions are produced in the NIST electron-beam ion trap (EBIT), extracted through a beamline that selects a single mass/charge species, then captured in a compact Penning trap. The magnetic field of the trap is generated by cylindrical NdFeB permanent magnets integrated into its electrodes. In a room-temperature prototype trap with a single NdFeB magnet, species including Ne10+ and N7+ were confined with storage times of order 1 second, showing the potential of this setup for manipulation and spectroscopy of highly charged ions in a controlled environment. Ion capture has since been demonstrated with similar storage times in a more-elaborate Penning trap that integrates two coaxial NdFeB magnets for improved B-field homogeneity. Ongoing experiments utilize a second-generation apparatus that incorporates this two-magnet Penning tra...

  4. Ultrasmall fluorescent ion-exchanging nanospheres containing selective ionophores.

    Science.gov (United States)

    Xie, Xiaojiang; Mistlberger, Günter; Bakker, Eric

    2013-10-15

    We present a convenient precipitation procedure to fabricate ultrasmall fluorescent ion-selective nanosensors that operate on the basis of bulk ion-exchange sensing principles. The nanosphere matrix is composed of bis(2-ethylhexyl) sebacate (DOS) and a triblock copolymer Pluronic(®) F-127, which also functions as a surfactant to stabilize the nanoparticle. The particles can be prepared easily in large quantity without resorting to further complicated purification. Dynamic light scattering shows that these particles have a monodisperse size distribution with an average diameter of ∼40 nm, suggesting that the nanoparticles are among the smallest ionophore-based ion-selective nanosensors reported to date. A newly reported oxazinoindoline (Ox) as well as a Nile blue derivative (chromoionophore I) was used as a chromoionophore. Na(+)- and H(+)-selective nanospheres were characterized by absorbance and fluorescence spectroscopy. Owing to the very small size of the nanospheres, the suspension containing the particles is transparent. In the additional presence of the pH indicator HPTS, spectroscopic interrogation of pH and Na(+) in the same sample was demonstrated. As an example, the nanospheres were used to measure the Na(+) level in commercial mineral waters, and the results showed good agreement with atomic absorption spectroscopy (AAS).

  5. HIGH DENSITY QCD WITH HEAVY-IONS

    CERN Multimedia

    The Addendum 1 to Volume 2 of the CMS Physics TDR has been published The Heavy-Ion analysis group completed the writing of a TDR summarizing the CMS plans in using heavy ion collisions to study high density QCD. The document was submitted to the LHCC in March and presented in the Open Session of the LHCC on May 9th. The study of heavy-ion physics at the LHC is promising to be very exciting. LHC will open a new energy frontier in ultra-relativistic heavy-ion physics. The collision energy of heavy nuclei at sNN = 5.5 TeV will be thirty times larger than what is presently available at RHIC. We will certainly probe quark and gluon matter at unprecedented values of energy density. The prime goal of this research programme is to study the fundamental theory of the strong interaction - Quantum Chromodynamics (QCD) - in extreme conditions of temperature, density and parton momentum fraction (low-x). Such studies, with impressive experimental and theoretical advances in recent years thanks to the wealth of high-qua...

  6. Ion and inhibitor binding of the double-ring ion selectivity filter of the mitochondrial calcium uniporter.

    Science.gov (United States)

    Cao, Chan; Wang, Shuqing; Cui, Tanxing; Su, Xun-Cheng; Chou, James J

    2017-04-04

    The calcium (Ca2+) uniporter of mitochondria is a holocomplex consisting of the Ca2+-conducting channel, known as mitochondrial calcium uniporter (MCU), and several accessory and regulatory components. A previous electrophysiology study found that the uniporter has high Ca2+ selectivity and conductance and this depends critically on the conserved amino acid sequence motif, DXXE (Asp-X-X-Glu) of MCU. A recent NMR structure of the MCU channel from Caenorhabditis elegans revealed that the DXXE forms two parallel carboxylate rings at the channel entrance that seem to serve as the ion selectivity filter, although direct ion interaction of this structural motif has not been addressed. Here, we use a paramagnetic probe, manganese (Mn2+), to investigate ion and inhibitor binding of this putative selectivity filter. Our paramagnetic NMR data show that mutants with a single carboxylate ring, NXXE (Asn-X-X-Glu) and DXXQ (Asp-X-X-Gln), each can bind Mn2+ specifically, whereas in the WT the two rings bind Mn2+ cooperatively, resulting in ∼1,000-fold higher apparent affinity. Ca2+ can specifically displace the bound Mn2+ at the DXXE site in the channel. Furthermore, titrating the sample with the known channel inhibitor ruthenium 360 (Ru360) can displace Mn2+ binding from the solvent-accessible Asp site but not the inner Glu site. The NMR titration data, together with structural analysis of the DXXE motif and molecular dynamics simulation, indicate that the double carboxylate rings at the apex of the MCU pore constitute the ion selectivity filter and that Ru360 directly blocks ion entry into the filter by binding to the outer carboxylate ring.

  7. Tuning the Solid Electrolyte Interphase for Selective Li- and Na-Ion Storage in Hard Carbon

    Energy Technology Data Exchange (ETDEWEB)

    Soto, Fernando A. [Department of Chemical Engineering, Texas A& M University, College Station TX 77843-3122 USA; Yan, Pengfei [Pacific Northwest National Laboratory, 902 Battelle Boulevard Richland WA 99354 USA; Engelhard, Mark H. [Pacific Northwest National Laboratory, 902 Battelle Boulevard Richland WA 99354 USA; Marzouk, Asma [Qatar Environment and Energy Research Institute, Hamad Bin Khalifa University, P.O. Box 5825 Doha Qatar; Wang, Chongmin [Pacific Northwest National Laboratory, 902 Battelle Boulevard Richland WA 99354 USA; Xu, Guiliang [Chemical Sciences and Engineering Division, Argonne National Laboratory, 9700 South Cass Avenue Argonne IL 60439 USA; Chen, Zonghai [Chemical Sciences and Engineering Division, Argonne National Laboratory, 9700 South Cass Avenue Argonne IL 60439 USA; Amine, Khalil [Chemical Sciences and Engineering Division, Argonne National Laboratory, 9700 South Cass Avenue Argonne IL 60439 USA; Liu, Jun [Pacific Northwest National Laboratory, 902 Battelle Boulevard Richland WA 99354 USA; Sprenkle, Vincent L. [Pacific Northwest National Laboratory, 902 Battelle Boulevard Richland WA 99354 USA; El-Mellouhi, Fedwa [Qatar Environment and Energy Research Institute, Hamad Bin Khalifa University, P.O. Box 5825 Doha Qatar; Balbuena, Perla B. [Department of Chemical Engineering, Texas A& M University, College Station TX 77843-3122 USA; Li, Xiaolin [Pacific Northwest National Laboratory, 902 Battelle Boulevard Richland WA 99354 USA

    2017-03-07

    Solid-electrolyte interphase (SEI) films with controllable properties are highly desirable for improving battery performance. In this paper, a combined experimental and theoretical approach is used to study SEI films formed on hard carbon in Li- and Na-ion batteries. It is shown that a stable SEI layer can be designed by precycling an electrode in a desired Li- or Na-based electrolyte, and that ionic transport can be kinetically controlled. Selective Li- and Na-based SEI membranes are produced using Li- or Na-based electrolytes, respectively. The Na-based SEI allows easy transport of Li ions, while the Li-based SEI shuts off Na-ion transport. Na-ion storage can be manipulated by tuning the SEI layer with film-forming electrolyte additives, or by preforming an SEI layer on the electrode surface. The Na specific capacity can be controlled to < 25 mAh g(-1); approximate to 1/10 of the normal capacity (250 mAh g(-1)). Unusual selective/ preferential transport of Li ions is demonstrated by preforming an SEI layer on the electrode surface and corroborated with a mixed electrolyte. This work may provide new guidance for preparing good ion-selective conductors using electrochemical approaches.

  8. Synthesis of ion-exchange resin for selective thorium and uranyl ions sorption

    Science.gov (United States)

    Konovalov, Konstantin; Sachkov, Victor

    2017-11-01

    In this work, the method of ion-exchange resin synthesis selective to radionuclides (uranium and thorium) is presented. The method includes synthesis of polymeric styrene-divinylbenzene macroporous matrix with size of 0.1-0.2 mm, and its subsequent transformation by nitration and then reduction by tin (II) chloride. For passivation of active primary amines partially oxidation by oxygen from air is used. Obtained ion-exchange resin has ratio of sorption sum U+Th to sorption sum of other total rare-earth elements as 1:1.88 at ratio of solid to liquid phase 1:200. The proposed method of ion-exchange resin synthesis is scaled-up for laboratory reactors with volume of 5 and 50 liters.

  9. A borane-bithiophene-BODIPY triad: intriguing tricolor emission and selective fluorescence response towards fluoride ions.

    Science.gov (United States)

    Sarkar, Samir Kumar; Thilagar, Pakkirisamy

    2013-10-04

    The structure and photophysical properties of a new triad (borane–bithiophene–BODIPY) 1 have been investigated. Triad 1 exhibits unprecedented tricolour emission when excited at the borane centred high energy absorption band and also acts as a selective fluorescent and colorimetric sensor for fluoride ions with ratiometric response. The experimental results are supported by computational studies.

  10. DETERMINATION OF STRONTIUM IONS IN WATERS WITH A HIGH CONTENT OF SODIUM IONS

    OpenAIRE

    Tatiana Mitina; Nadejda Bondarenco; Diana Grigoras; Elena Botizat; Tudor Lupascu

    2015-01-01

    This paper reports on the influence of sodium ions on experimental determination of strontium ions concentration in waters with a high content of sodium ions by using emission flame photometry and atomic absorption spectroscopy. For the method of emission flame photometry it was shown that at a wavelength of 460.7 nm (spectral emission line of strontium) the emission is linearly dependent on the concentration of sodium ions. The greatest impact of high concentrations of sodium ions on the res...

  11. An Electrochemical Sensor Based on Novel Ion Imprinted Polymeric Nanoparticles for Selective Detection of Lead Ions

    Directory of Open Access Journals (Sweden)

    Masoud Ghanei-Motlagh

    1999-11-01

    Full Text Available In this study, the novel surface ion-imprinted polymer (IIP particles were prepared and applied as a electrode modifier in stripping voltammetric detection of lead(II ion. A carbon paste electrode (CPE modified with IIP nanoparticles and multi-walled carbon nanotubes (MWCNTs was used for accumulation of toxic lead ions. Various factors that govern on electrochemical signals including carbon paste composition, pH of the preconcentration solution, supporting electrolyte, stirring time, reduction potential and time were studied in detail. The best electrochemical response for Pb(II ions was obtained with a paste composition of 7% (w/w of lead IIP, 10% MWCNTs, 53% (w/w of graphite powder and 30% (w/w of paraffin oil using a solution of 0.1 mol L-1 acetat buffer solution (pH=4.5 with a extraction time of 15 min. A sensitive response for Pb(II ions in the concentration range of 3 to 55 µg L-1 was achived. The proposed electrochemical sensor showed low detection limit (0.5 µg L-1, remarkable selectivity and good reproducibility (RSD = 3.1%. Determination of lead(II content in different environmental water samples was also realized adopting graphite furnace atomic absorptions spectrometry (GF-AAS and the obtained results were satisfactory.

  12. Selectivity of calix[4]arene-bis(benzocrown-6) in the complexation and transport of francium ion.

    Science.gov (United States)

    Haverlock, Tamara J; Mirzadeh, Saed; Moyer, Bruce A

    2003-02-05

    It is shown for the first time that a representative member of the "cesium-selective" calix[4]arene-crown-6 family exhibits a high affinity for Fr+ ion. In the investigation, the transport of 221Fr+ and Cs+ ions by calix[4]arene-bis(benzocrown-6) from an aqueous sodium nitrate solution into the water-immiscible diluent 1,2-dichloroethane was measured and compared to address the question of selectivity of the calix-crown-6 cavity toward alkali metal ions of increasing size. Selective separation of 221Fr+ from its parent 225Ac and from the matrix Na+ ions was demonstrated. Higher distribution ratios were obtained than those for the Cs+ ion. The extraction equilibria were determined for the case of the Cs+ ion, and the same equilibria were shown to be applicable to the case of Fr+ with inclusion of additional competitive effects.

  13. Integrated ion imprinted polymers-paper composites for selective and sensitive detection of Cd(II) ions

    Energy Technology Data Exchange (ETDEWEB)

    Huang, Kai [State Key Laboratory of Environment Health - Incubation, Key Laboratory of Environment and Health, Ministry of Education, Key Laboratory of Environment and Health Wuhan, Ministry of Environmental Protection, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, #13 Hangkong Road, Hubei, 430030, Wuhan (China); Chen, Ying [Hubei Center for Disease Control and Prevention, No. 6 ZhuoDao Quan North Road, 430079, Wuhan (China); Zhou, Feng [State Key Laboratory of Environment Health - Incubation, Key Laboratory of Environment and Health, Ministry of Education, Key Laboratory of Environment and Health Wuhan, Ministry of Environmental Protection, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, #13 Hangkong Road, Hubei, 430030, Wuhan (China); Zhao, Xiaoya [Hubei Entry-Exit Inspection and Quarantine Bureau of PRC, No.588 Qingtaidadao Road, Hubei, 430022, Wuhan (China); Liu, Jiafa [Hubei Center for Disease Control and Prevention, No. 6 ZhuoDao Quan North Road, 430079, Wuhan (China); Mei, Surong; Zhou, Yikai [State Key Laboratory of Environment Health - Incubation, Key Laboratory of Environment and Health, Ministry of Education, Key Laboratory of Environment and Health Wuhan, Ministry of Environmental Protection, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, #13 Hangkong Road, Hubei, 430030, Wuhan (China); Jing, Tao, E-mail: jingtao@hust.edu.cn [State Key Laboratory of Environment Health - Incubation, Key Laboratory of Environment and Health, Ministry of Education, Key Laboratory of Environment and Health Wuhan, Ministry of Environmental Protection, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, #13 Hangkong Road, Hubei, 430030, Wuhan (China)

    2017-07-05

    Highlights: • IIPs are first grafted on the low-cost A4 print paper to develop an integrated paper-based device. • As an imprinted composite, the adsorption capacity is 155.2 mg g{sup –1} and the imprinted factor is more than 3.0. • As an analytical method, the limit of detection is 0.4 ng mL{sup –1}. • Based on the water quality standards, it could be used to determine Cd(II) ions in drinking water. - Abstract: Paper-based sensor is a new alternative technology to develop a portable, low-cost, and rapid analysis system in environmental chemistry. In this study, ion imprinted polymers (IIPs) using cadmium ions as the template were directly grafted on the surface of low-cost print paper based on the reversible addition-fragmentation chain transfer polymerization. It can be applied as a recognition element to selectively capture the target ions in the complex samples. The maximum adsorption capacity of IIPs composites was 155.2 mg g{sup –1} and the imprinted factor was more than 3.0. Then, IIPs-paper platform could be also applied as a detection element for highly selective and sensitive detection of Cd(II) ions without complex sample pretreatment and expensive instrument, due to the selective recognition, formation of dithizone-cadmium complexes and light transmission ability. Under the optimized condition, the linear range was changed from 1 to 100 ng mL{sup –1} and the limit of detection was 0.4 ng mL{sup –1}. The results were in good agreement with the classic ICP-MS method. Furthermore, the proposed method can also be developed for detection of other heavy metals by designing of new IIPs.

  14. Superheated water ion-exchange chromatography: an experimental approach for interpretation of separation selectivity in ion-exchange processes.

    Science.gov (United States)

    Shibukawa, Masami; Shimasaki, Tomomi; Saito, Shingo; Yarita, Takashi

    2009-10-01

    Cation-exchange selectivity for alkali and alkaline-earth metal ions and tetraalkylammonium ions on a strongly acidic sulfonic acid cation-exchange resin has been investigated in the temperature range of 40-175 degrees C using superheated water chromatography. Dependence of the distribution coefficient (ln KD) on the reciprocal of temperature (1/T) is not linear for most of the ions studied, and the selectivity coefficient for a pair of alkali metal ions or that of alkaline-earth metal ions approaches unity as temperature increases. On the other hand, the retention order of tetraalkylammonium ions is reversed at 160 degrees C or above when eluted with Na2SO4 aqueous solution and the larger ions are eluted faster than the smaller ones contrary to the retention order obtained at ambient temperature. The change in ion-exchange selectivity with temperature observed with superheated water chromatography has been discussed on the basis of the effect of temperature on hydration of the ions and specific adsorption or distribution of ionic species between the external solution and ion-exchange resin. In superheated water, the electrostatic interaction or association of the ions with the fixed ion becomes a predominant mechanism resulting in different separation selectivity from that obtained at ambient temperature.

  15. One-pot green synthesis of high quantum yield oxygen-doped, nitrogen-rich, photoluminescent polymer carbon nanoribbons as an effective fluorescent sensing platform for sensitive and selective detection of silver(I) and mercury(II) ions.

    Science.gov (United States)

    Wang, Zhong-Xia; Ding, Shou-Nian

    2014-08-05

    This work reports on a facile, economical, and green preparative strategy toward water-soluble, fluorescent oxygen-doped, nitrogen-rich, photoluminescent polymer carbon nanoribbons (ONPCRs) with a quantum yield of approximately 25.61% by the hydrothermal process using uric acid as a carbon-nitrogen source for the first time. The as-prepared fluorescent ONPCRs showed paddy leaf-like structure with 80-160 nm length and highly efficient fluorescent quenching ability in the presence of mercury(II) (Hg(2+)) or silver (Ag(+)) ions due to the formed nonfluorescent metal complexes via robust Hg(2+)-O or Ag(+)-N interaction with the O and N of fluorescent ONPCRs, which allowed the analysis of Hg(2+) and Ag(+) ions in a very simple method. By employing this sensor, excellent linear relationships existed between the quenching degree of the ONPCRs and the concentrations of Hg(2+) and Ag(+) ions in the range of 2.0 nM to 60 μM and 5.0 nM to 80 μM, respectively. By using ethylenediaminetetraacetate and ammonia as the masking agent of Hg(2+) and Ag(+) ions, respectively, Hg(2+) or Ag(+) ions were exclusively detected in coexistence with Ag(+) or Hg(2+) ions with high sensitivity, and the detection limits as low as 0.68 and 1.73 nM (3σ) were achieved, respectively, which also provided a reusable detection method for Hg(2+) and Ag(+) ions. Therefore, the easily synthesized fluorescent ONPCRs may have great potential applications in the detection of Hg(2+) and Ag(+) ions for biological assay and environmental protection.

  16. Discrimination of Swiss cheese from 5 different factories by high impact volatile organic compound profiles determined by odor activity value using selected ion flow tube mass spectrometry and odor threshold.

    Science.gov (United States)

    Taylor, Kaitlyn; Wick, Cheryl; Castada, Hardy; Kent, Kyle; Harper, W James

    2013-10-01

    Swiss cheese contains more than 200 volatile organic compounds (VOCs). Gas chromatography-mass spectrometry has been utilized for the analysis of volatile compounds in food products; however, it is not sensitive enough to measure VOCs directly in the headspace of a food at low concentrations. Selected ion flow tube mass spectrometry (SIFT-MS) provides a basis for determining the concentrations of VOCs in the head space of the sample in real time at low concentration levels of parts per billion/trillion by volume. Of the Swiss cheese VOCs, relatively few have a major impact on flavor quality. VOCs with odor activity values (OAVs) (concentration/odor threshold) greater than one are considered high-impact flavor compounds. The objective of this study was to utilize SIFT-MS concentrations in conjunction with odor threshold values to determine OAVs thereby identifying high-impact VOCs to use for differentiating Swiss cheese from five factories and identify the factory variability. Seventeen high-impact VOCs were identified for Swiss cheese based on an OAV greater than one in at least 1 of the 5 Swiss cheese factories. Of these, 2,3-butanedione was the only compound with significantly different OAVs in all factories; however, cheese from any pair of factories had multiple statistically different compounds based on OAV. Principal component analysis using soft independent modeling of class analogy statistical differentiation plots, with all of the OAVs, showed differentiation between the 5 factories. Overall, Swiss cheese from different factories was determined to have different OAV profiles utilizing SIFT-MS to determine OAVs of high impact compounds. © 2013 Institute of Food Technologists®

  17. High Affinity Binding of Indium and Ruthenium Ions by Gastrins.

    Directory of Open Access Journals (Sweden)

    Graham S Baldwin

    Full Text Available The peptide hormone gastrin binds two ferric ions with high affinity, and iron binding is essential for the biological activity of non-amidated forms of the hormone. Since gastrins act as growth factors in gastrointestinal cancers, and as peptides labelled with Ga and In isotopes are increasingly used for cancer diagnosis, the ability of gastrins to bind other metal ions was investigated systematically by absorption spectroscopy. The coordination structures of the complexes were characterized by extended X-ray absorption fine structure (EXAFS spectroscopy. Changes in the absorption of gastrin in the presence of increasing concentrations of Ga3+ were fitted by a 2 site model with dissociation constants (Kd of 3.3 x 10-7 and 1.1 x 10-6 M. Although the absorption of gastrin did not change upon the addition of In3+ ions, the changes in absorbance on Fe3+ ion binding in the presence of indium ions were fitted by a 2 site model with Kd values for In3+ of 6.5 x 10-15 and 1.7 x 10-7 M. Similar results were obtained with Ru3+ ions, although the Kd values for Ru3+ of 2.6 x 10-13 and 1.2 x 10-5 M were slightly larger than observed for In3+. The structures determined by EXAFS all had metal:gastrin stoichiometries of 2:1 but, while the metal ions in the Fe, Ga and In complexes were bridged by a carboxylate and an oxygen with a metal-metal separation of 3.0-3.3 Å, the Ru complex clearly demonstrated a short range Ru-Ru separation, which was significantly shorter, at 2.4 Å, indicative of a metal-metal bond. We conclude that gastrin selectively binds two In3+ or Ru3+ ions, and that the affinity of the first site for In3+ or Ru3+ ions is higher than for ferric ions. Some of the metal ion-gastrin complexes may be useful for cancer diagnosis and therapy.

  18. High Affinity Binding of Indium and Ruthenium Ions by Gastrins.

    Science.gov (United States)

    Baldwin, Graham S; George, Graham N; Pushie, M Jake

    2015-01-01

    The peptide hormone gastrin binds two ferric ions with high affinity, and iron binding is essential for the biological activity of non-amidated forms of the hormone. Since gastrins act as growth factors in gastrointestinal cancers, and as peptides labelled with Ga and In isotopes are increasingly used for cancer diagnosis, the ability of gastrins to bind other metal ions was investigated systematically by absorption spectroscopy. The coordination structures of the complexes were characterized by extended X-ray absorption fine structure (EXAFS) spectroscopy. Changes in the absorption of gastrin in the presence of increasing concentrations of Ga3+ were fitted by a 2 site model with dissociation constants (Kd) of 3.3 x 10-7 and 1.1 x 10-6 M. Although the absorption of gastrin did not change upon the addition of In3+ ions, the changes in absorbance on Fe3+ ion binding in the presence of indium ions were fitted by a 2 site model with Kd values for In3+ of 6.5 x 10-15 and 1.7 x 10-7 M. Similar results were obtained with Ru3+ ions, although the Kd values for Ru3+ of 2.6 x 10-13 and 1.2 x 10-5 M were slightly larger than observed for In3+. The structures determined by EXAFS all had metal:gastrin stoichiometries of 2:1 but, while the metal ions in the Fe, Ga and In complexes were bridged by a carboxylate and an oxygen with a metal-metal separation of 3.0-3.3 Å, the Ru complex clearly demonstrated a short range Ru-Ru separation, which was significantly shorter, at 2.4 Å, indicative of a metal-metal bond. We conclude that gastrin selectively binds two In3+ or Ru3+ ions, and that the affinity of the first site for In3+ or Ru3+ ions is higher than for ferric ions. Some of the metal ion-gastrin complexes may be useful for cancer diagnosis and therapy.

  19. High current injector for heavy ion fusion

    Science.gov (United States)

    Yu, S.; Eylon, S.; Chupp, W. W.

    1993-05-01

    A 2 MV, 800 mA, K(+) injector for heavy ion fusion studies is under construction. This new injector is a one-beam version of the proposed 4-beam ILSE injector. A new 36-module MARX is being built to achieve a 5 micro-s flat top. The high voltage generator is stiff (less than 5k Omega) to minimize effects of beam-induced transients. A large (approximately 7 in. diameter) curved hot alumina-silicate source emits a 1 micro-s long beam pulse through a gridless extraction electrode, and the ions are accelerated to 1 MV in a diode configuration. Acceleration to 2 MV takes place in a set of electrostatic quadrupole (ESQ) units, arranged to simultaneously focus and accelerate the ion beam. Heavy shields and other protection devices have been built in to minimize risks of high voltage breakdown. Beam aberration effects through the ESQ have been studied extensively with theory, simulations, and scaled experiments. The design, simulations, experiments, and engineering of the ESQ injector will be presented.

  20. Selective Liquid-Liquid Extraction of Lead Ions Using Newly Synthesized Extractant 2-(Dibutylcarbamoylbenzoic Acid

    Directory of Open Access Journals (Sweden)

    Hossein Soltani

    2015-12-01

    Full Text Available A new carboxylic acid extractant, named 2-(dibutylcarbamoylbenzoic acid, is prepared and its potential for selective solvent extraction and recovery of lead ions from industrial samples was investigated. The slope analysis indicated that the lead ions are extracted by formation of 1:2 metal to ligand complexes. The effect of the parameters influencing the extraction efficiency including kind of the organic diluent, extractant concentration, type of the salt used for ionic strength adjustment, contact time and temperature was evaluated and discussed. Under optimized conditions (aqueous phase: 5 ml, initial lead concentration 1 × 10-4 M, pH 4, sodium chloride 0.1 M; organic phase: 5 ml dichloromethane, ligand concentration 0.05 M, a quantitative (75.2 ± 0.8% and highly selective extraction of lead ions in the presence of zinc, nickel, cobalt and cadmium ions (each 1 × 10-4 M was achieved, after 20 min. magnetically stirring of the phases, at      25 °C. The extracted lead ions were stripped from the organic phase by diluted nitric acid (0.1 M solution. The proposed method was successfully applied for separation of lead from industrial samples. The study of the effect of temperature allowed evaluating the thermodynamic parameters of the extraction process of lead ions by the studied extractant into dichloromethane.

  1. Transverse microanalysis of high energy Ion implants

    Energy Technology Data Exchange (ETDEWEB)

    Dooley, S.P.; Jamieson, D.N.; Nugent, K.W.; Prawer, S. [Melbourne Univ., Parkville, VIC (Australia). School of Physics

    1996-12-31

    High energy ion implants in semiconductor materials have been analyzed by Channeling Contrast Microscopy (CCM) perpendicular to the implant direction, allowing imaging of the entire ion track. The damage produced by Channeled and Random 1.4 MeV H{sup +} implants into the edge of a <100> type IIa diamond wafer were analyzed by channeling into the face of the crystal. The results showed negligible damage in the surface region of the implants, and swelling induced misalignment at the end of range of the implants. Channeled 1.4 MeV H{sup +} implants in diamond had a range only 9% deeper than Random implants, which could be accounted for by dechanneling of the beam. The channeling of H{sup +}{sub 2} ions has been previously found to be identical to that of protons of half energy, however the current experiment has shown a 1% increase in {chi}{sub min} for H{sup +}{sub 2} in diamond compared to H{sup +} at 1,2 MeV per proton. This is due to repulsion between protons within the same channel. 5 refs., 2 figs.

  2. Precision mass measurements of highly charged ions

    Science.gov (United States)

    Kwiatkowski, A. A.; Bale, J. C.; Brunner, T.; Chaudhuri, A.; Chowdhury, U.; Ettenauer, S.; Frekers, D.; Gallant, A. T.; Grossheim, A.; Lennarz, A.; Mane, E.; MacDonald, T. D.; Schultz, B. E.; Simon, M. C.; Simon, V. V.; Dilling, J.

    2012-10-01

    The reputation of Penning trap mass spectrometry for accuracy and precision was established with singly charged ions (SCI); however, the achievable precision and resolving power can be extended by using highly charged ions (HCI). The TITAN facility has demonstrated these enhancements for long-lived (T1/2>=50 ms) isobars and low-lying isomers, including ^71Ge^21+, ^74Rb^8+, ^78Rb^8+, and ^98Rb^15+. The Q-value of ^71Ge enters into the neutrino cross section, and the use of HCI reduced the resolving power required to distinguish the isobars from 3 x 10^5 to 20. The precision achieved in the measurement of ^74Rb^8+, a superallowed β-emitter and candidate to test the CVC hypothesis, rivaled earlier measurements with SCI in a fraction of the time. The 111.19(22) keV isomeric state in ^78Rb was resolved from the ground state. Mass measurements of neutron-rich Rb and Sr isotopes near A = 100 aid in determining the r-process pathway. Advanced ion manipulation techniques and recent results will be presented.

  3. Rapid determination of trace level copper in tea infusion samples by solid contact ion selective electrode

    Directory of Open Access Journals (Sweden)

    Aysenur Birinci

    2016-07-01

    Full Text Available A new solid contact copper selective electrode with a poly (vinyl chloride (PVC membrane consisting of o-xylylenebis(N,N-diisobutyldithiocarbamate as ionophore has been prepared. The main novelties of constructed ion selective electrode concept are the enhanced robustness, cheapness, and fastness due to the use of solid contacts. The electrode exhibits a rapid (< 10 seconds and near-Nernstian response to Cu2+ activity from 10−1 to 10−6 mol/L at the pH range of 4.0–6.0. No serious interference from common ions was found. The electrode characterizes by high potential stability, reproducibility, and full repeatability. The electrode was used as an indicator electrode in potentiometric titration of Cu(II ions with EDTA and for the direct assay of tea infusion samples by means of the calibration graph technique. The results compared favorably with those obtained by the atomic absorption spectroscopy (AAS.

  4. 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.

  5. Selective observation of charge storing ions in supercapacitor electrode materials.

    Science.gov (United States)

    Forse, Alexander C; Griffin, John M; Grey, Clare P

    2017-11-04

    Nuclear magnetic resonance (NMR) spectroscopy has emerged as a useful technique for probing the structure and dynamics of the electrode-electrolyte interface in supercapacitors, as ions inside the pores of the carbon electrodes can be studied separately from bulk electrolyte. However, in some cases spectral resolution can limit the information that can be obtained. In this study we address this issue by showing how cross polarisation (CP) NMR experiments can be used to selectively observe the in-pore ions in supercapacitor electrode materials. We do this by transferring magnetisation from 13C nuclei in porous carbons to nearby nuclei in the cations (1H) or anions (19F) of an ionic liquid. Two-dimensional NMR experiments and CP kinetics measurements confirm that in-pore ions are located within Ångströms of sp2-hybridised carbon surfaces. Multinuclear NMR experiments hold promise for future NMR studies of supercapacitor systems where spectral resolution is limited. Copyright © 2017 University of Cambridge. Published by Elsevier Inc. All rights reserved.

  6. [Thermodynamic approach to the selection of polyuronide sequestrants for the protection of the human body from toxic metal ions. Interactions of polyuronides with strontium and calcium ions].

    Science.gov (United States)

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

    2001-01-01

    Selectivity of polyuronide sequestrants (pectate, alginates of various uronide composition) in respect to Sr2+ and Ca2+ ions has been evaluated in terms of thermodynamic affinity. It is suggested that there is no point in the use of pectate as a Sr(2+)-binding agent because at initial stages of reaction it reveals higher affinity to Ca2+ ions in comparison to Sr2+ ions. Contrary to pectate, alginates under similar conditions have higher affinity to Sr2+ ions. It is shown that these ions are bound only by blocks of L-guluronic acid residues in alginate macromolecules. The results obtained lend support to the advisability of the use of alginate preparations with the high content of L-guluronic acid residues for the excretion of Sr2+ ions from human body.

  7. Ion Exchange Selectivity of Nafion Films on Electrode Surfaces.

    Science.gov (United States)

    1984-05-01

    linked, while -10- -. * "* ... .. . *. *.Ref ion is not. The Gibbs-Donnan equation (the fundamental thermodynamic equation for exchange reactions (29...as evidenced by the nearly complete disappearance of the Fe3+/2+ voltamoetric wave. (To minimize hydrolysis and couplexation effects, 0.25 M HClO4 was...at this point clear why Nation has such high affinities for these complexes. While from a thermodynamic point of view, Nafion appears to be an ideal

  8. Surprisingly high activity for oxygen reduction reaction of selected oxides lacking long oxygen-ion diffusion paths at intermediate temperatures: a case study of cobalt-free BaFeO(3-δ).

    Science.gov (United States)

    Dong, Feifei; Chen, Yubo; Chen, Dengjie; Shao, Zongping

    2014-07-23

    The widespread application of solid oxide fuel cell technology requires the development of innovative electrodes with high activity for oxygen reduction reaction (ORR) at intermediate temperatures. Here, we demonstrate that a cobalt-free parent oxide BaFeO(3-δ) (BF), which lacks long-range oxygen-ion diffusion paths, has surprisingly high electrocatalytic activity for ORR. Both in situ high-temperature X-ray diffraction analysis on room-temperature powder and transmission electron microscopy on quenched powder are applied to investigate the crystal structure of BF. Despite the lack of long oxygen-ion diffusion paths, the easy redox of iron cations as demonstrated by thermal gravimetric analysis (TGA) and oxygen temperature-programmed desorption and the high oxygen vacancy concentration as supported by iodometric titration and TGA benefit the reduction of oxygen to oxygen ions. Moreover, the electrical conductivity relaxation technique in conjunction with a transient thermogravimetric study reveals very high surface exchange kinetics of BF oxide. At 700 °C, the area specific resistance of BF cathode, as expressed by a symmetrical cell configuration, is only ∼0.021 Ω cm(2), and the derived single fuel cell achieves high power output with a peak power density of 870 mW cm(-2). It suggests that an undoped BF parent oxide can be used as a high-efficiency catalyst for ORR.

  9. Green, Water-Dispersible Photoluminescent On-Off-On Probe for Selective Detection of Fluoride Ions.

    Science.gov (United States)

    Singhal, Pallavi; Vats, Bal Govind; Jha, Sanjay K; Neogy, Suman

    2017-06-21

    Considering the high toxicity and widespread availability of fluoride ions in different environmental matrices, it is imperative to design a probe for its detection. In view of this, a selective fluorescent on-off-on probe based on carbon quantum dots (CQDs) and Eu3+ has been designed. We have synthesized water-soluble carboxylic acid-functionalized CQDs and monitored their interaction with Eu3+. Luminescence quenching in the CQD emission was observed (switch-off) on adding Eu3+ ions. We investigate the reason for this luminescence quenching using time-resolved emission and high-resolution transmission electron microscopy (HRTEM) studies and observed that both electron transfer from CQDs to Eu3+ and aggregation of CQDs are responsible for the luminescence quenching. ζ-Potential and X-ray photoelectron spectroscopy studies confirm Eu3+ binding with the COOH groups on CQD surface. Interestingly, luminescence regains after the addition of fluoride ions to the CQDs/Eu3+ system (switch-on). This has been assigned to the removal of Eu3+ from the CQD surface due to the formation of EuF3 and is confirmed by X-ray diffraction and HRTEM measurements. The sensitivity of the probe was tested by carrying out experiments with other competing ions and was found to be selective for fluoride ions. Experiments with variable concentrations of fluoride ions suggest that the working range of the probe is 1-25 ppm. The probe has been successfully tested for the detection of fluoride ions in a toothpaste sample and the results were compared to those of ion chromatography. To the best of our knowledge, this is the first report based on CQDs and Eu3+ for the detection of fluoride ions, wherein a clear mechanism of the detection has been demonstrated, which, in turn, will help to develop better detection methods. The suggested probe is green, economical, rapid, efficient, and, most importantly, selective and can be used for the detection of fluoride ions in real environmental samples.

  10. Electrochemical evidences and consequences of significant differences in ions diffusion rate in polyacrylate-based ion-selective membranes.

    Science.gov (United States)

    Woźnica, Emilia; Mieczkowski, Józef; Michalska, Agata

    2011-11-21

    The origin and effect of surface accumulation of primary ions within the ion-selective poly(n-butyl acrylate)-based membrane, obtained by thermal polymerization, is discussed. Using a new method, based on the relation between the shape of a potentiometric plot and preconditioning time, the diffusion of copper ions in the membrane was found to be slow (the diffusion coefficient estimated to be close to 10(-11) cm(2) s(-1)), especially when compared to ion-exchanger counter ions--sodium cations diffusion (a diffusion coefficient above 10(-9) cm(2) s(-1)). The higher mobility of sodium ions than those of the copper-ionophore complex results in exposed ion-exchanger role leading to undesirably exposed sensitivity to sodium or potassium ions.

  11. Charged solvatochromic dyes as signal transducers in pH independent fluorescent and colorimetric ion selective nanosensors.

    Science.gov (United States)

    Xie, Xiaojiang; Gutiérrez, Agustín; Trofimov, Valentin; Szilagyi, Istvan; Soldati, Thierry; Bakker, Eric

    2015-10-06

    Ionophore-based ion selective optical nanosensors that operate independently of the sample pH are developed here by the use of electrically charged solvatochromic dyes as signal transducers. A series of dye molecules with a D-π-A structure was synthesized and characterized in various solvents and incorporated into ion selective nanospheres for K(+), Na(+), and H(+). Since dye leakage was greatly suppressed when the solvatochromic dyes were encapsulated in the nanosphere core, ion sensing nanospheres were explored for cellular ion imaging in Dictyostelium discoideum live cells but spontaneous dye loss resulted in undesired staining of cells. The in vitro analysis of potassium in human plasma was successfully demonstrated with this approach. A theoretical model was developed for the response of the ion selective nanosensors containing charged solvatochromic dyes. The nanosensors exhibited a tunable response range, high sensitivity, and good stability.

  12. 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.

  13. Highly Supersonic Ion Pulses in a Collisionless Magnetized Plasma

    DEFF Research Database (Denmark)

    Juul Rasmussen, Jens; Schrittwieser, R.

    1982-01-01

    The initial transient response of a collisionless plasma to a high positive voltage step is investigated. Four different pulses are observed. An electron plasma wave pulse is followed by an ion burst. The latter is overtaken and absorbed by a highly supersonic ion pulse. Thereafter, an ion...

  14. Highly Compressed Ion Beams for High Energy Density Science

    CERN Document Server

    Friedman, Alex; Briggs, Richard J; Callahan, Debra; Caporaso, George; Celata, C M; Davidson, Ronald C; Faltens, Andy; Grant-Logan, B; Grisham, Larry; Grote, D P; Henestroza, Enrique; Kaganovich, Igor D; Lee, Edward; Lee, Richard; Leitner, Matthaeus; Nelson, Scott D; Olson, Craig; Penn, Gregory; Reginato, Lou; Renk, Tim; Rose, David; Sessler, Andrew M; Staples, John W; Tabak, Max; Thoma, Carsten H; Waldron, William; Welch, Dale; Wurtele, Jonathan; Yu, Simon

    2005-01-01

    The Heavy Ion Fusion Virtual National Laboratory (HIF-VNL) is developing the intense ion beams needed to drive matter to the High Energy Density (HED) regimes required for Inertial Fusion Energy (IFE) and other applications. An interim goal is a facility for Warm Dense Matter (WDM) studies, wherein a target is heated volumetrically without being shocked, so that well-defined states of matter at 1 to 10 eV are generated within a diagnosable region. In the approach we are pursuing, low to medium mass ions with energies just above the Bragg peak are directed onto thin target "foils," which may in fact be foams or "steel wool" with mean densities 1% to 100% of solid. This approach complements that being pursued at GSI, wherein high-energy ion beams deposit a small fraction of their energy in a cylindrical target. We present the requirements for warm dense matter experiments, and describe suitable accelerator concepts, including novel broadband traveling wave pulse-line, drift-tube linac, RF, and single-gap approa...

  15. Highly charged ion based time of flight emission microscope

    Science.gov (United States)

    Barnes, Alan V.; Schenkel, Thomas; Hamza, Alex V.; Schneider, Dieter H.; Doyle, Barney

    2001-01-01

    A highly charged ion based time-of-flight emission microscope has been designed, which improves the surface sensitivity of static SIMS measurements because of the higher ionization probability of highly charged ions. Slow, highly charged ions are produced in an electron beam ion trap and are directed to the sample surface. The sputtered secondary ions and electrons pass through a specially designed objective lens to a microchannel plate detector. This new instrument permits high surface sensitivity (10.sup.10 atoms/cm.sup.2), high spatial resolution (100 nm), and chemical structural information due to the high molecular ion yields. The high secondary ion yield permits coincidence counting, which can be used to enhance determination of chemical and topological structure and to correlate specific molecular species.

  16. Production of High Energy Ions Near an Ion Thruster Discharge Hollow Cathode

    Science.gov (United States)

    Katz, Ira; Mikellides, I. G.; Goebel, D. M.; Jameson, K. K.; Wirz, R.; Polk, James E.

    2006-01-01

    Several researchers have measured ions leaving ion thruster discharge chambers with energies far greater than measured discharge chamber potentials. Presented in this paper is a new mechanism for the generation of high energy ions and a comparison with measured ion spectra. The source of high energy ions has been a puzzle because they not only have energies in excess of measured steady state potentials, but as reported by Goebel et. al. [1], their flux is independent of the amplitude of time dependent plasma fluctuations. The mechanism relies on the charge exchange neutralization of xenon ions accelerated radially into the potential trough in front of the discharge cathode. Previous researchers [2] have identified the importance of charge exchange in this region as a mechanism for protecting discharge cathode surfaces from ion bombardment. This paper is the first to identify how charge exchange in this region can lead to ion energy enhancement.

  17. Physics with Highly-Charged Ions in an EBIT

    Science.gov (United States)

    Crespo López-Urrutia, J. R.; Bapat, B.; Draganić, I.; Feuerstein, B.; Fischer, D.; Lörch, H.; Moshammer, R.; Ullrich, J.; DuBois, R. D.; Zou, Y.

    After the commissioning of the Freiburg electron beam ion trap, experiments on dielectronic recombination of the low-lying resonances in He-like Ar16+ have been carried out at high resolution. Forbidden transitions (``coronal lines'') of highly charged argon ions in the optical range have been measured with an accuracy around 1 ppm. Ions extracted from FreEBIT have been used to perform collision experiments using the Cold Target Recoil-Ion Momentum Spectroscopy (COLTRIMS) technique.

  18. A novel ion selective sensor for promethium determination

    Energy Technology Data Exchange (ETDEWEB)

    Gupta, Vinod K., E-mail: vinodfcy@iitr.ernet.in [Department of Chemistry, Indian Institute of Technology Roorkee, Roorkee 247 667 (India); Chemistry Department, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia); Jain, Rajeev [School of Studies in Chemistry, Jiwaji University, Gwalior 474011 (India); Hamdan, A.J. [Chemistry Department, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia); Agarwal, Shilpi [School of Studies in Chemistry, Jiwaji University, Gwalior 474011 (India); Bharti, Arvind K. [Department of Chemistry, Indian Institute of Technology Roorkee, Roorkee 247 667 (India)

    2010-11-29

    This is a first promethium{sup 145} ion-selective sensor based on the comparative study of two Schiff base ligands (X{sub 1} and X{sub 2}) as neutral ionophores. Effect of various plasticizers: 2-nitrophenyloctylether (o-NPOE), dibutyl phosphonate (DBP), dioctylphthalate (DOP), tri-(2-ethylhexyl) phosphate (TEHP), dibutyl butylphosphonate (DBBP), chloronaphthalene (CN) and anion excluders: potassium tetrakis (p-chloropheny1) borate (KTpClPB), sodiumtetraphenylborate (NaTPB) and oleic acid (OA) have been studied. The membrane with a composition of ionophore (X{sub 1}/X{sub 2}):KTpClPB:PVC:o-NPOE (w/w, %) in the ratio of 5:5:30:60 exhibited best performance. The best responsive membrane sensors (8 and 21) exhibited working concentration range of 4.5 x 10{sup -7}-1.0 x 10{sup -2} M and 3.5 x 10{sup -6}-1.0 x 10{sup -2} M with a detection limits of 3.2 x 10{sup -7} M and 2.3 x 10{sup -6} M and Nernstian slopes of 20.0 {+-} 0.5, 19.5 {+-} 0.5 mV decade{sup -1} of activity, respectively. The sensor no. 8 works satisfactorily in partially non-aqueous media up to 10% (v/v) content of methanol, ethanol and acetonitrile. Analytical application of the proposed sensor has been demonstrated in determination of promethium (III) ions in spiked water samples.

  19. Ion-selective formation of a guanine quadruplex on DNA origami structures.

    Science.gov (United States)

    Olejko, Lydia; Cywinski, Piotr J; Bald, Ilko

    2015-01-07

    DNA origami nanostructures are a versatile tool that can be used to arrange functionalities with high local control to study molecular processes at a single-molecule level. Here, we demonstrate that DNA origami substrates can be used to suppress the formation of specific guanine (G) quadruplex structures from telomeric DNA. The folding of telomeres into G-quadruplex structures in the presence of monovalent cations (e.g. Na(+) and K(+)) is currently used for the detection of K(+) ions, however, with insufficient selectivity towards Na(+). By means of FRET between two suitable dyes attached to the 3'- and 5'-ends of telomeric DNA we demonstrate that the formation of G-quadruplexes on DNA origami templates in the presence of sodium ions is suppressed due to steric hindrance. Hence, telomeric DNA attached to DNA origami structures represents a highly sensitive and selective detection tool for potassium ions even in the presence of high concentrations of sodium ions. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  20. Bis(sulfonamide) transmembrane carriers allow pH-gated inversion of ion selectivity.

    Science.gov (United States)

    Roy, Arundhati; Biswas, Oindrila; Talukdar, Pinaki

    2017-03-09

    Bis(sulfonamide) based synthetic carriers are reported for inversion of ion selectivity upon deviation of pH within a narrow window. A liposomal membrane potential is also generated when potassium ions are passively transported by these carriers.

  1. Histamine selectively potentiates acid-sensing ion channel 1a.

    Science.gov (United States)

    Nagaeva, Elina I; Tikhonova, Tatiana B; Magazanik, Lev G; Tikhonov, Denis B

    2016-10-06

    Although acid-sensitive ion channels (ASICs) play an important role in brain functions, the exact mechanism of their physiological activation remain unclear. A possible answer to the intriguing question is that some presently unknown endogenous ligand(s) positively modulate ASICs and enhance their responses to physiologically significant level. In the present work we found that histamine selectively potentiates ASIC1a homomers in CHO cells. Action of histamine was particularly pronounced at modest acidifications, which cause minor response. At these conditions micromolar concentrations of histamine have provided significant potentiation of ASIC1a response. We proposed that histamine and possibly some other endogenous amines can positively modulate ASICs functions. Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.

  2. Magnetic mesoporous thiourea-formaldehyde resin as selective adsorbent: A simple and highly-sensitive electroanalysis strategy for lead ions in drinking water and milk by solid state-based anodic stripping.

    Science.gov (United States)

    Zhao, Yanfang; Xu, Lubin; Liu, Min; Duan, Zhiqiang; Wang, Hua

    2018-01-15

    A simple and sensitive electroanalysis method has been developed for the direct determination of lead ions of nanomolar levels in real samples of drinking water and milk by employing magnetic mesoporous thiourea-formaldehyde resin (TUF@Fe 3 O 4 ) nanocomposites as the capturing absorbents. Here, the prepared TUF@Fe 3 O 4 with the large-surface-area mesoporous structure and strong Pb 2+ -binding ligands could facilitate the selective and large-scale adsorption of Pb 2+ ions from the complex sample matrices to be further magnetically separated onto the magnetic electrodes. Moreover, the Pb 2+ ions magnetically accumulated were electrochemically measured alternatively by the solid state-based anodic stripping of PbCl 2 . The detection limit was found to be 0.0070nmolL -1 . The as-developed Pb 2+ electroanalysis method with the magnetic electrodes and TUF@Fe 3 O 4 nanocomposites could avoid the complicated sample preparation and electrode modification, thus holding the great potential of applications for the Pb 2+ detection in different real samples. Copyright © 2017 Elsevier Ltd. All rights reserved.

  3. Thin layer coulometry with ionophore based ion-selective membranes.

    Science.gov (United States)

    Grygolowicz-Pawlak, Ewa; Bakker, Eric

    2010-06-01

    We are demonstrating here for the first time a thin layer coulometric detection mode for ionophore based liquid ion-selective membranes. Coulometry promises to achieve the design of robust, calibration free sensors that are especially attractive for applications where recalibration in situ is difficult or undesirable. This readout principle is here achieved with porous polypropylene tubing doped with the membrane material and which contains a chlorinated silver wire in the inner compartment, together with the fluidically delivered sample solution. The membrane material consists of the lipophilic plasticizer dodecyl 2-nitrophenyl ether, the lipophilic electrolyte ETH 500, and the calcium ionophore ETH 5234. Importantly and in contrast to earlier work on voltammetric liquid membrane electrodes, the membrane also contains a cation-exchanger salt, KTFPB. This renders the membrane permselective and allows one to observe open circuit potentiometric responses for the device, which is confirmed to follow the expected Nernstian equation. Moreover, as the same cationic species is now potential determining at both interfaces of the membrane, it is possible to use rapidly diffusing and/or thin membrane systems where transport processes at the inner and outer interface of the membrane do not perturb each other or the overall composition of the membrane. The tubing is immersed in an electrolyte solution where the counter and working electrode are placed, and the potentials are applied relative to the measured open circuit potentials. Exhaustive current decays are observed in the range of 10 to 100 muM calcium chloride. The observed charge, calculated as integrated currents, is linearly dependent on concentration and forms the basis for the coulometric readout of ion-selective membrane electrodes.

  4. Selective detection of heavy metal ions by self assembled chemical field effect transistors

    Energy Technology Data Exchange (ETDEWEB)

    Ruan, Hang, E-mail: hruan@nanosonic.com; Kang, Yuhong; Gladwin, Elizabeth; Claus, Richard O. [NanoSonic, Inc., 158 Wheatland Drive, Pembroke, Virginia 24136 (United States)

    2015-04-20

    Multiple layer-by-layer sensor material modifications were designed and implemented to achieve selectivity of semiconductor based chemical field effect transistors (ChemFETs) to particular heavy metal ions. The ChemFET sensors were fabricated and modified in three ways, with the intent to initially target first mercury and lead ions and then chromium ions, respectively. Sensor characterization was performed with the gate regions of the sensor elements exposed to different concentrations of target heavy metal ion solutions. A minimum detection level in the range of 0.1 ppm and a 10%–90% response time of less than 10 s were demonstrated. By combining layer-by-layer gold nanoparticles and lead ionophores, a sensor is produced that is sensitive and selective not only to chromium but also to Cr{sup 3+} and Cr{sup 6+}. This result supports the claim that high selectivity can be achieved by designing self-assembled bonding for lead, arsenic, chromium, cesium, mercury, and cadmium.

  5. 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.

  6. A high energy, heavy ion microprobe for ion beam research on the tandem accelerator at ANSTO

    Energy Technology Data Exchange (ETDEWEB)

    Cohen, D.D.; Siegele, R.; Dytlewski, N.

    1996-04-01

    A comprehensive review is given on the production and use of heavy ion beams with spot sizes of a few {mu}m. The development of a high energy, heavy ion microprobe at ANSTO and its possible applications are discussed. The microprobe is designed to focus a wide range of ion beam types, from light ions such as protons up to ions as heavy as iodine. Details of the ion beam optics, optical calculations and a description of the proposed microbeam design are given. The unique combination of high energy, heavy ions and improved detection systems will provide high sensitivity elemental composition and depth profiling information, allowing surface topography and 3D surface reconstruction to be performed on a broad range of materials. 86 refs., 5 tabs., 15 figs.

  7. High efficiency direct detection of ions from resonance ionization of sputtered atoms

    Science.gov (United States)

    Gruen, Dieter M.; Pellin, Michael J.; Young, Charles E.

    1986-01-01

    A method and apparatus are provided for trace and other quantitative analysis with high efficiency of a component in a sample, with the analysis involving the removal by ion or other bombardment of a small quantity of ion and neutral atom groups from the sample, the conversion of selected neutral atom groups to photoions by laser initiated resonance ionization spectroscopy, the selective deflection of the photoions for separation from original ion group emanating from the sample, and the detection of the photoions as a measure of the quantity of the component. In some embodiments, the original ion group is accelerated prior to the RIS step for separation purposes. Noise and other interference are reduced by shielding the detector from primary and secondary ions and deflecting the photoions sufficiently to avoid the primary and secondary ions.

  8. Strain-tolerant High Capacity Silicon Anodes via Directed Lithium Ion Transport for High Energy Density Lithium-ion Batteries

    Science.gov (United States)

    Goldman, Jason

    2012-02-01

    Energy storage is an essential component of modern technology, with applications including public infrastructure, transportation systems, and consumer electronics. Lithium-ion batteries are the preeminent form of energy storage when high energy / moderate power densities are required. Improvements to lithium-ion battery energy / power density through the adoption of silicon anodes—with approximately an order of magnitude greater gravimetric capacity than traditional carbon-based anodes--have been limited by ˜300% strains during electrochemical lithium insertion which result in short operational lifetimes. In two different systems we demonstrated improvements to silicon-based anode performance via directed lithium ion transport. The first system demonstrated a crystallographic-dependent anisotropic electrochemical lithium insertion in single-crystalline silicon anode microstructures. Exploiting this anisotropy, we highlight model silicon anode architectures that limit the maximum strain during electrochemical lithium insertion. This self-strain-limiting is a result of selecting a specific microstructure design such that during lithiation the anisotropic evolution of strain, above a given threshold, blocks further lithium intercalation. Exemplary design rules have achieved self-strain-limited charging capacities ranging from 677 mAhg-1 to 2833 mAhg-1. A second system with variably encapsulated silicon-based anodes demonstrated greater than 98% of their initial capacity after 130+ cycles. This anode also can operate stably at high energy/power densities. A lithium-ion battery with this anode was able to continuously (dis)charge in 10 minutes, corresponding to a power / energy density of ˜1460 W/kg and ˜243 Wh/kg--up to 780% greater power density and 220% higher energy density than conventional lithium-ion batteries. Anodes were also demonstrated with areal capacities of 12.7 mAh/cm^2, two orders of magnitude greater than traditional thin-film silicon anodes.[4pt

  9. Characterization of structure and function of ZS-9, a K+ selective ion trap.

    Science.gov (United States)

    Stavros, Fiona; Yang, Alex; Leon, Alejandro; Nuttall, Mark; Rasmussen, Henrik S

    2014-01-01

    Hyperkalemia, a condition in which serum potassium ions (K+) exceed 5.0 mmol/L, is a common electrolyte disorder associated with substantial morbidity. Current methods of managing hyperkalemia, including organic polymer resins such as sodium polystyrene sulfonate (SPS), are poorly tolerated and/or not effective. Sodium zirconium cyclosilicate (ZS-9) is under clinical development as an orally administered, non-absorbed, novel, inorganic microporous zirconium silicate compound that selectively removes excess K+ in vivo. The development, structure and ion exchange properties of ZS-9 and its hypothesized mechanism of action are described. Based on calculation of the interatomic distances between the atoms forming the ZS-9 micropores, the size of the pore opening was determined to be ∼ 3 Å (∼ diameter of unhydrated K+). Unlike nonspecific organic polymer resins like SPS, the ZS-9 K+ exchange capacity (KEC) was unaffected by the presence of calcium (Ca2+) or magnesium ions (Mg2+) and showed>25-fold selectivity for K+ over either Ca2+ or Mg2+. Conversely, the selectivity of SPS for K+ was only 0.2-0.3 times its selectivity for Ca2+ or Mg2+in mixed ionic media. It is hypothesized that the high K+ specificity of ZS-9 is attributable to the chemical composition and diameter of the micropores, which possibly act in an analogous manner to the selectivity filter utilized by physiologic K+ channels. This hypothesized mechanism of action is supported by the multi-ion exchange studies. The effect of pH on the KEC of ZS-9 was tested in different media buffered to mimic different portions of the human gastrointestinal tract. Rapid K+ uptake was observed within 5 minutes - mainly in the simulated small intestinal and large intestinal fluids, an effect that was sustained for up to 1 hour. If approved, ZS-9 will represent a novel, first-in-class therapy for hyperkalemia with improved capacity, selectivity, and speed for entrapping K+ when compared to currently available options.

  10. High-Resolution Ion Cyclotron Mobility Spectrometry

    Science.gov (United States)

    Merenbloom, Samuel I.; Glaskin, Rebecca S.; Henson, Zachary B.; Clemmer, David E.

    2009-01-01

    A novel ion mobility spectrometry instrument incorporating a cyclotron geometry drift tube is presented. The drift tube consists of eight regions, four curved drift tubes and four ion funnels. Packets of ions are propagated around the drift tube by changing the drift field at a frequency that is resonant with the ion’s drift time through each region. The approach trims each packet of ions as it leaves and enters each new region. An electrostatic gate allows ions to be kept in the drift tube for numerous cycles, increasing the ability to resolve specified ions. We demonstrate the approach by isolating the [M+2H]2+ or [M+3H]3+ charge state of substance P as well as individual trisaccharide isomers from a mixture of melezitose and raffinose. Resolving powers in excess of 300 are obtainable with this approach. PMID:19143495

  11. Laboratory Evaluation of Ion-Selective Electrodes for Simultaneous Analysis of Macronutrients in Hydroponic Solution

    Science.gov (United States)

    Automated sensing of macronutrients in hydroponic solution would allow more efficient management of nutrients for crop growth in closed hydroponic systems. Ion-selective microelectrode technology requires an ion-selective membrane or a solid metal material that responds selectively to one analyte in...

  12. Dynamic electrochemistry with ionophore based ion-selective membranes

    OpenAIRE

    Crespo Paravano, Gaston Adrian; Bakker, Eric

    2013-01-01

    This review outlines key principles and recent advances in the use of dynamic electrochemistry with polymeric liquid membranes. Ideally polarizable membranes are most attractive in fundamental studies of ion transfer and when the accumulation of the ion in the receiving phase is of key interest, for example in stripping ion transfer voltammetry. All solid-state membranes doped with conducting polymers have exhibited attractive low detection limit for hydrophilic ions. On the other hand, initi...

  13. Dynamic electrochemistry with ionophore based ion-selective membranes

    OpenAIRE

    Crespo Gastón Adrián; Bakker Eric

    2013-01-01

    This review outlines key principles and recent advances in the use of dynamic electrochemistry with polymeric liquid membranes. Ideally polarizable membranes are most attractive in fundamental studies of ion transfer and when the accumulation of the ion in the receiving phase is of key interest for example in stripping ion transfer voltammetry. All solid state membranes doped with conducting polymers have exhibited attractive low detection limit for hydrophilic ions. On the other hand initial...

  14. Voltammetric ion-selective electrodes for the selective determination of cations and anions.

    Science.gov (United States)

    Zhang, Jie; Harris, Alexander R; Cattrall, Robert W; Bond, Alan M

    2010-03-01

    A general theory has been developed for voltammetric ion sensing of cations and anions based on the use of an electrode coated with a membrane containing an electroactive species, an ionophore, and a supporting electrolyte dissolved in a plasticizer. In experimental studies, a membrane coated electrode is fabricated by the drop coating method. In one configuration, a glassy carbon electrode is coated with a poly(vinyl chloride) based membrane, which contains the electroactive species, ionophore, plasticizer and supporting electrolyte. In the case of a cation sensor, ionophore facilitated transfer of the target cation from the aqueous solution to the membrane phase occurs during the course of the reduction of the electroactive species present in the membrane in order to maintain charge neutrality. The formal potential is calculated from the cyclic voltammogram as the average of the reduction and oxidation peak potentials and depends on the identity and concentration of the ion present in the aqueous solution phase. A plot of the formal potential versus the logarithm of the concentration exhibits a close to Nernstian slope of RT/F millivolts per decade change in concentration when the concentration of K(+) and Na(+) is varied over the concentration range of 0.1 mM to 1 M when K(+) or Na(+) ionophores are used in the membrane. The slope is close to RT/2F millivolts for a Ca(2+) voltammetric ion-selective electrode fabricated using a Ca(2+) ionophore. The sensor measurement time is only a few seconds. Voltammetric sensors for K(+), Na(+), and Ca(2+) constructed in this manner exhibit the sensitivity and selectivity required for determination of these ions in environmentally and biologically important matrixes. Analogous principles apply to the fabrication of anion voltammetric sensors.

  15. Ion trapping in the high-energy storage ring HESR

    Energy Technology Data Exchange (ETDEWEB)

    Hinterberger, Frank [Bonn Univ. (Germany). Helmholtz-Institut fuer Strahlen- und Kernphysik

    2011-10-15

    The problem of ion trapping in the high-energy storage ring HESR is studied in the present report. Positive ions are trapped in the negative potential well of the antiproton beam. The ions are produced by the interaction between the antiproton beam and the residual gas. The adverse effects of ion trapping like tune shifts, tune spreads and coherent instabilities are reviewed. The ion production rate by ionization of the residual gas molecules is estimated. The negative potential well and the corresponding electric fields of the antiproton beam are evaluated in order to study the transverse and longitudinal motion of the ions and the accumulation in trapping pockets. The removal of ions can be achieved using clearing electrodes and under certain conditions resonant transverse beam shaking. Diagnostic tools and measurements of trapped ion effects are sketched. (orig.)

  16. Structural and thermodynamic properties of selective ion binding in a K+ channel.

    Directory of Open Access Journals (Sweden)

    Steve W Lockless

    2007-05-01

    Full Text Available Thermodynamic measurements of ion binding to the Streptomyces lividans K(+ channel were carried out using isothermal titration calorimetry, whereas atomic structures of ion-bound and ion-free conformations of the channel were characterized by x-ray crystallography. Here we use these assays to show that the ion radius dependence of selectivity stems from the channel's recognition of ion size (i.e., volume rather than charge density. Ion size recognition is a function of the channel's ability to adopt a very specific conductive structure with larger ions (K(+, Rb(+, Cs(+, and Ba(2+ bound and not with smaller ions (Na(+, Mg(2+, and Ca(2+. The formation of the conductive structure involves selectivity filter atoms that are in direct contact with bound ions as well as protein atoms surrounding the selectivity filter up to a distance of 15 A from the ions. We conclude that ion selectivity in a K(+ channel is a property of size-matched ion binding sites created by the protein structure.

  17. Production of intense negative hydrogen beams with polarized nuclei by selective neutralization of cold negative ions

    Science.gov (United States)

    Hershcovitch, A.

    1984-02-13

    A process for selectively neutralizing H/sup -/ ions in a magnetic field to produce an intense negative hydrogen ion beam with spin polarized protons. Characteristic features of the process include providing a multi-ampere beam of H/sup -/ ions that are

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

    DEFF Research Database (Denmark)

    Larsen, Erik Huusfeldt; Hansen, Sven Hedegaard

    1992-01-01

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

  19. Multi-energy ion implantation from high-intensity laser

    Directory of Open Access Journals (Sweden)

    Cutroneo Mariapompea

    2016-06-01

    Full Text Available The laser-matter interaction using nominal laser intensity above 1015 W/cm2 generates in vacuum non-equilibrium plasmas accelerating ions at energies from tens keV up to hundreds MeV. From thin targets, using the TNSA regime, plasma is generated in the forward direction accelerating ions above 1 MeV per charge state and inducing high-ionization states. Generally, the ion energies follow a Boltzmann-like distribution characterized by a cutoff at high energy and by a Coulomb-shift towards high energy increasing the ion charge state. The accelerated ions are emitted with the high directivity, depending on the ion charge state and ion mass, along the normal to the target surface. The ion fluencies depend on the ablated mass by laser, indeed it is low for thin targets. Ions accelerated from plasma can be implanted on different substrates such as Si crystals, glassy-carbon and polymers at different fluences. The ion dose increment of implanted substrates is obtainable with repetitive laser shots and with repetitive plasma emissions. Ion beam analytical methods (IBA, such as Rutherford backscattering spectroscopy (RBS, elastic recoil detection analysis (ERDA and proton-induced X-ray emission (PIXE can be employed to analyse the implanted species in the substrates. Such analyses represent ‘off-line’ methods to extrapolate and to character the plasma ion stream emission as well as to investigate the chemical and physical modifications of the implanted surface. The multi-energy and species ion implantation from plasma, at high fluency, changes the physical and chemical properties of the implanted substrates, in fact, many parameters, such as morphology, hardness, optical and mechanical properties, wetting ability and nanostructure generation may be modified through the thermal-assisted implantation by multi-energy ions from laser-generated plasma.

  20. Selective zinc ion detection by functionalised ZnO nanorods with ionophore

    Science.gov (United States)

    Ibupoto, Z. H.; Usman Ali, Syed M.; Chey, C. O.; Khun, K.; Nur, O.; Willander, Magnus

    2011-11-01

    In this paper, highly dense and well aligned single-crystal zinc oxide nanorods were grown along the c-axis on a gold coated glass substrate using a low temperature aqueous chemical growth approach. The prepared ZnO nanorods were functionalized with plastic membrane coatings containing specific ionophore (12-crown-4) which is highly selective to zinc ions (Zn+2). The electrochemical response of the sensor was found to be linear over a relatively wide logarithmic concentration range from 1 μM to 100 mM. The proposed sensor showed a good linearity with a high sensitivity of ˜35 mV/decade for sensing Zn+2 ions. A fast response time of less than 5 s with a good selectivity, repeatability, reproducibility, and negligible response to common interferents ions such as calcium (Ca2+), magnesium (Mg2+), or potassium (K+), and iron (Fe+3) and copper (Cu+2) was also demonstrated. Moreover, the proposed sensor showed good stoichiometric results for potentiometric titration.

  1. Site Selective Spectroscopy on Erbium Ions in Stoichiometric Lithium Tantalate

    Energy Technology Data Exchange (ETDEWEB)

    Miyahara, K; Toulouse, A; Woodward, N; Capek, P; Dierolf, V, E-mail: vod2@lehigh.ed [Physics Department Lehigh University, Bethlehem, PA 18015 (United States)

    2010-11-01

    Ferroelectric materials such as lithium niobate (LiNbO{sub 3}) and the isostructural lithium tantalate (LiTaO{sub 3}) play an important role in integrated optics since they allow the possibility to combine their favourable electro-optical, acousto-optical, and nonlinear properties with the ability to add additional functional groups by doping. Examples are rare earth ions that act as active centres for laser and optical amplifier applications. We present our sites-selective spectroscopic studies on Er{sup 3+} doped nearly stoichiometric LiTaO{sub 3} that include results about the assignment of excitation and emission peaks to different sites, symmetry properties of these sites, energy transfer among major sites, and up-conversion efficiencies. We compare the results in LiTiO{sub 3} with the corresponding ones in the much better studied LiNbO{sub 3} host and find that the type of centres and their spectral feature are very similar.

  2. Nitrogen doped carbon nanodots as fluorescent probes for selective detection and quantification of Ferric(III) ions

    Science.gov (United States)

    Chin, Suk-Fun; Tan, Shao-Chien; Pang, Suh-Cem; Ng, Sing-Muk

    2017-11-01

    Nitrogen (N) doped carbon dots (N-CDs) that showed blue fluorescence with quantum yield (QY) of 12.25% were synthesized by one step microwave irradiation of lysine in ortho-phosphoric acid at 1000 W for 5 min. The as-synthesized N-CDs were successfully explored as fluorescent probes for selective detection of ferric (Fe3+) ions in aqueous condition with a linear range from 0.2 to 5.0 mM and a detection limit of 0.074 mM ± 0.081 (S/N = 3). The N-CDs exhibited high selectivity towards the detection of Fe3+ ions even in the presence of interfering ions. The N-CDs also demonstrated the potential of practical application for determining of Fe3+ ions concentration in real samples with high recovery rate and low relative standard deviation error.

  3. Novel Lithium Ion High Energy Battery Project

    Data.gov (United States)

    National Aeronautics and Space Administration — Under this SBIR project a new chemistry for Li-ion cells will be developed that will enable a major advance in secondary battery gravimetric and volumetric energy...

  4. Fragmentation of very high energy heavy ions

    CERN Document Server

    Giorgini, M

    2001-01-01

    A stack of CR39 (C12H18O7)n nuclear track detectors with a Cu target was exposed to a 158 A GeV lead ion beam at the CERN-SPS, in order to study the fragmentation properties of lead nuclei. Measurements of the total, break-up and pick-up charge-changing cross sections of ultrarelativistic Pb ions on Cu and CR39 targets are presented and discussed.

  5. Highly charged ion injector in the terminal of tandem accelerator

    Energy Technology Data Exchange (ETDEWEB)

    Matsuda, M; Asozu, T; Nakanoya, T; Kutsukake, K; Hanashima, S; Takeuchi, S, E-mail: matsuda.makoto@jaea.go.j [Japan Atomic Energy Agency, Tokai Research and Development Center, Nuclear Science Research Institute, Tandem Accelerator Section 2-4 Shirakata-Shirane, Tokai, Naka, Ibaraki, 319-1195 (Japan)

    2009-04-01

    A highly charged heavy ion injector using an all permanent magnet type electron cyclotron resonance ion source (ECRIS) has been constructed in the high voltage terminal of the vertical and folded type 20UR Pelletron tandem accelerator at Japan Atomic Energy Agency at Tokai. The new in-terminal injector made it possible to accelerate highly charged heavy ions which have not been obtained from the tandem accelerator. Beam energy and beam intensity have been remarkably increased and the noble gas ion beams have become available.

  6. Polymer-Supported Reagents: The Role of Bifunctionality in the Design of Ion-Selective Complexants

    Energy Technology Data Exchange (ETDEWEB)

    Alexandratos, S. D.

    2001-06-01

    The importance of multi-functionality in the preparation of ion-selective polymers is evident from the structure of enzymes where specific metal ions are bound through cooperative interactions among different amino acids. In synthetic polymers, ionic selectivity is enhanced when a chemical reaction is superimposed on an ion-exchange process. The concept of reactive ion exchange has been extended through the synthesis of crosslinked polymers whose metal ion selectivity is a function of reduction, coordination or precipitation reactions as determined by various covalently bound ligands. Development of three classes of dual mechanism bifunctional polymers, a new series of bifunctional diphosphonate polymers, and novel bifunctional ion-selective polymers with enhanced ionic accessibility has been accomplished.

  7. Ion current detector for high pressure ion sources for monitoring separations

    Energy Technology Data Exchange (ETDEWEB)

    Smith, R.D.; Wahl, J.H.; Hofstadler, S.A.

    1996-08-13

    The present invention relates generally to any application involving the monitoring of signal arising from ions produced by electrospray or other high pressure (>100 torr) ion sources. The present invention relates specifically to an apparatus and method for the detection of ions emitted from a capillary electrophoresis (CE) system, liquid chromatography, or other small-scale separation methods. And further, the invention provides a very simple diagnostic as to the quality of the separation and the operation of an electrospray source. 7 figs.

  8. Ion current detector for high pressure ion sources for monitoring separations

    Energy Technology Data Exchange (ETDEWEB)

    Smith, Richard D. (Richland, WA); Wahl, Jon H. (Richland, WA); Hofstadler, Steven A. (Richland, WA)

    1996-01-01

    The present invention relates generally to any application involving the monitoring of signal arising from ions produced by electrospray or other high pressure (>100 torr) ion sources. The present invention relates specifically to an apparatus and method for the detection of ions emitted from a capillary electrophoresis (CE) system, liquid chromatography, or other small-scale separation methods. And further, the invention provides a very simple diagnostic as to the quality of the separation and the operation of an electrospray source.

  9. Ion imprinted activated carbon solid-phase extraction coupled to flame atomic absorption spectrometry for selective determination of lead ions in environmental samples

    Energy Technology Data Exchange (ETDEWEB)

    Naraghi, Kiyana; Panahi, Homayon Ahmad; Hassani, Amir Hesam [Islamic Azad University, Tehran (Korea, Republic of); Moniri, Elham [Islamic Azad University, Varamin (Iran, Islamic Republic of)

    2014-10-15

    A simple lead ion imprinted sorbent was synthesized by coupling activated carbon with a known metal chelating compound, iminodiacetic acid. The ion imprinted sorbent has been characterized using Fourier transform infrared spectroscopy, elemental analysis and thermogravimetric analysis and subjected for the extraction and determination of trace Pb(II) in environmental water samples. The optimum pH value for sorption of the lead ion was 6.5. The sorption capacity of lead imprinted sorbent was 42.2 mg g{sup −1}. The chelating imprinted sorbent can be reused for five cycles of sorption-desorption without any significant change in sorption capacity. Compared with non-imprinted polymer particles, the lead ion imprinted sorbent showed high adsorption capacity, significant selectivity, good site accessibility for Pb(II). The equilibrium adsorption data of Pb(II) by modified resin were analyzed by Langmuir, Freundlich, Temkin and Redlich-Peterson models.

  10. Cryogenic linear Paul trap for cold highly charged ion experiments

    DEFF Research Database (Denmark)

    Schwarz, Maria; Versolato, Oscar; Windberger, Alexander

    2012-01-01

    Storage and cooling of highly charged ions require ultra-high vacuum levels obtainable by means of cryogenic methods. We have developed a linear Paul trap operating at 4 K capable of very long ion storage times of about 30 h. A conservative upper bound of the H2 partial pressure of about 10−15 mbar...

  11. Physics with Highly-Charged Ions in an EBIT

    Energy Technology Data Exchange (ETDEWEB)

    Crespo Lopez-Urrutia, J. R.; Bapat, B.; Draganic, I.; Feuerstein, B.; Fischer, D.; Loerch, H.; Moshammer, R.; Ullrich, J. [Max-Planck-Insitut fuer Kernphysik (Germany); DuBois, R. D. [University of Missoury (United States); Zou, Y. [Fudan University (China)

    2003-03-15

    After the commissioning of the Freiburg electron beam ion trap, experiments on dielectronic recombination of the low-lying resonances in He-like Ar{sup 16+} have been carried out at high resolution. Forbidden transitions ('coronal lines') of highly charged argon ions in the optical range have been measured with an accuracy around 1 ppm. Ions extracted from FreEBIT have been used to perform collision experiments using the Cold Target Recoil-Ion Momentum Spectroscopy (COLTRIMS) technique.

  12. Lead ion-selective electrodes based on polyphenylenediamine as unique solid ionophores.

    Science.gov (United States)

    Huang, Mei-Rong; Rao, Xue-Wu; Li, Xin-Gui; Ding, Yong-Bo

    2011-09-15

    A novel membrane electrode for Pb(II) ion detection based on semi-conducting poly(m-phenylenediamine) microparticles as a unique solid ionophore was fabricated. The electrode exhibited significantly enhanced response towards Pb(II) over the concentration range from 3.16×10(-6) to 0.0316 M at pH 3.0-5.0 with a low detection limit of 6.31×10(-7) M, a high sensitivity displaying a near-Nernstian slope of 29.8 mV decade(-1) for Pb(II). The electrode showed a long lifetime of 5 months and a short response time of 14s. A systematical investigation on the effect of anion excluder and various foreign ions on the selectivity of the electrode by a fixed interference method suggests that all other metal ions hardly ever interfere with the determination of Pb(II) except high concentration Hg(II). The electrode was successfully used as an indicator electrode in the potentiometric titration of Pb(II) with EDTA. Furthermore, the electrode has been used to satisfactorily analyze four types of real-world samples like spiked human urine, spiked tap water, and river water containing interfering ions like Na(I), Ca(II), Mg(II), Zn(II), Pd(II), Fe(III), K(I), Cu(II) and Hg(II) up to 8.04×10(-4) M, demonstrating fast response, high selectivity, good recovery (96.6-121.4%), good repeatability (RSD 0.31-6.45%), and small relative error (5.0%). Copyright © 2011 Elsevier B.V. All rights reserved.

  13. ECR ion source for high current linac

    CERN Document Server

    Cui Bao Qun; Jiang Wei; LiLiQiang; WangRongWen

    2002-01-01

    An intense ECR ion source for ADS (accelerator driven sub-critical system) is described. Two configurations of the source has been developed and tested. 100 mA hydrogen beam has been extracted from the ion source at 30 keV, the proton ratio is greater than 85%, estimated emittance is 0.11 pi mm centre dot mrad, the maximum extracted beam density is 340 mA/cm sup 2 . A 100 hours reliability test of the source is also described

  14. Estimation of ion-site association constants in ion-selective electrode membranes by modified segmented sandwich membrane method

    Energy Technology Data Exchange (ETDEWEB)

    Peshkova, Maria A.; Korobeynikov, Anton I.; Mikhelson, Konstantin N. [St. Petersburg State University, St. Petersburg (Russian Federation)

    2008-08-01

    A method aimed at potentiometric estimation of the association of ions with ion-exchanger sites and charged ionophores in ion-selective electrode membranes is proposed. The method relies on the measurements of segmented sandwich membrane potentials. It is shown theoretically that the quantification of ion association requires use of weakly associated ionic additive whose concentration in the working segment of the sandwich must be varied. This is in contrast with well-established technique of ion to neutral ionophore complexation measurements. The advantages and limitations of the novel method are critically evaluated. Association of ions in plasticized poly(vinylchloride) membranes is studied experimentally. Experimental results are provided related to the association of K{sup +}, Na{sup +}, Cs{sup +}, and NH{sub 4}{sup +}, and also Ca{sup 2+} with commonly used sites: tetra(p-Cl-phenyl)borate anion and calcium-selective lipophilic ion-exchanger bis[4-(1,1,3,3-tetramethylbutyl)phenyl]phosphate. (author)

  15. A napthelene-pyrazol conjugate: Al(III) ion-selective blue shifting chemosensor applicable as biomarker in aqueous solution.

    Science.gov (United States)

    Mukherjee, Manjira; Pal, Siddhartha; Lohar, Somenath; Sen, Buddhadeb; Sen, Supriti; Banerjee, Samya; Banerjee, Snehasis; Chattopadhyay, Pabitra

    2014-10-07

    A newly synthesized and crystalographically characterized napthelene–pyrazol conjugate, 1-[(5-phenyl-1H-pyrazole-3-ylimino)-methyl]-naphthalen-2-ol (HL) behaves as an Al(III) ion-selective chemosensor through internal charge transfer (ICT)-chelation-enhanced fluorescence (CHEF) processes in 100 mM HEPES buffer (water–DMSO 5:1, v/v) at biological pH with almost no interference of other competitive ions. This mechanism is readily studied from electronic, fluorimetric and (1)H NMR titration. The probe (HL) behaved as a highly selective fluorescent sensor for Al(III) ions as low as 31.78 nM within a very short response time (15–20 s). The sensor (HL), which has no cytotoxicity, is also efficient in detecting the distribution of Al(III) ions in HeLa cells via image development under fluorescence microscope.

  16. Graphene quantum dots-terbium ions as novel sensitive and selective time-resolved luminescent probes.

    Science.gov (United States)

    Llorent-Martínez, Eulogio J; Durán, Gema M; Ríos, Ángel; Ruiz-Medina, Antonio

    2018-01-01

    We propose an alternative approach for the development of analytical methods based on terbium-sensitized luminescence (TSL). TSL is based on the complexation between Tb(III) ions and fluorescent organic compounds that have appropriate functional groups to complex with Tb(III). We report the use of graphene quantum dot (GQDs) nanoparticles to improve the sensitivity and selectivity of TSL detection. GQDs can react with terbium ions through the carboxylic groups present in their structure. These Tb(III)-GQD complexes, formed in situ in aqueous solution, can be used as time-resolved luminescent probes. Ascorbic acid was selected as a target analyte to demonstrate the suitability of the proposed method. The selectivity of the TSL method was highly improved for most of the interferences tested. Under the optimum conditions [Tb(III) concentration 5 × 10-4 mol L-1, GQD concentration 4 mg L-1], a minimum 100% increase in selectivity was observed for several vitamins and common cations that may be present in the samples to be analyzed. In addition, the analytical signal showed a 30% enhancement with the use of GQDs compared with the use of merely Tb(III) ions, with a detection limit of 0.12 μg mL-1. The repeatability and intermediate precision were lower than 3% and 5%, respectively. From the results obtained, the implementation of GQDs in TSL can lead to the development of novel time-resolved luminescent probes with high analytical potential. Graphical abstract Quenching of Tb(III)-graphene quantum dot (GQD) luminescence by ascorbic acid (AA). TBL terbium-sensitized luminescence.

  17. Comparative studies of ONNO-based ligands as ionophores for palladium ion-selective membrane sensors.

    Science.gov (United States)

    Gupta, Vinod K; Goyal, Rajendra N; Sharma, Ram A

    2009-04-30

    Palladium sensors based on two neutral ionophores, N,N'-bis(acetylacetone) cyclohexanediamine (L(1)) and N,N'-bis(o-hydroxyacetophenone)-1,2-cyclohexanediamine (L(2)) for quantification of palladium ions are described. Effect of various plasticizers (o-NPOE, DBP, DEP, DOP, TBP, and CN) and anion excluder, sodium tetra phenyl borate (NaTPB) has been studied. The best performance is obtained with a membrane composition of PVC:o-NPOE:ionophore (L(1)):NaTPB of 150:300:5:5 (%, w/w). The sensor exhibits significantly enhanced selectivity towards palladium ion over the concentration range 1.0 x 10(-8) to 1.0 x 10(-1)M with a lower detection limit of 4.0 x 10(-9)M and a Nernstian compliance (29.1+/-0.3 mV decade(-1) of activity) within pH range 2.0-6.0 and fast response time of 10s. Influence of the membrane composition and possible interfering ions has also been investigated on the response properties of the electrode. Fast and stable response, good reproducibility and long-term stability of the sensor are demonstrated. The sensor has been found to work satisfactorily in partially non-aqueous media up to 20% (v/v) content of methanol, ethanol and acetonitrile and could be used for a period of 4 months. Selectivity coefficients determined with fixed interference method (FIM) indicate high selectivity for palladium. The proposed electrode shows fairly good discrimination of palladium from other cations. The application of prepared sensor has been demonstrated in determination of palladium ions in spiked water sample.

  18. Selective Binding, Self-Assembly and Nanopatterning of the Creutz-Taube Ion on Surfaces

    Directory of Open Access Journals (Sweden)

    Qingling Hang

    2009-02-01

    Full Text Available The surface attachment properties of the Creutz-Taube ion, i.e., [(NH35Ru(pyrazineRu(NH35]5+, on both hydrophilic and hydrophobic types of surfaces were investigated using X-ray photoelectron spectroscopy (XPS. The results indicated that the Creutz-Taube ions only bound to hydrophilic surfaces, such as SiO2 and –OH terminated organic SAMs on gold substrates. No attachment of the ions on hydrophobic surfaces such as –CH3 terminated organic SAMs and poly(methylmethacrylate (PMMA thin films covered gold or SiO2 substrates was observed. Further ellipsometric, atomic force microscopy (AFM and time-dependent XPS studies suggested that the attached cations could form an inorganic analog of the self-assembled monolayer on SiO2 substrate with a “lying-down” orientation. The strong electrostatic interaction between the highly charged cations and the anionic SiO2 surface was believed to account for these observations. Based on its selective binding property, patterning of wide (~200 nm and narrow (~35 nm lines of the Creutz-Taube ions on SiO2 surface were demonstrated through PMMA electron resist masks written by electron beam lithography (EBL.

  19. 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.

  20. High Performance Pillared Vanadium Oxide Cathode for Lithium Ion Batteries

    Science.gov (United States)

    2015-04-24

    Performance Pillared Vanadium Oxide Cathode for Lithium Ion Batteries Siu on Tung, Krista L. Hawthorne, Yi Ding, James Mainero, and Levi T. Thompson...Automotive Research Development and Engineering Center, Warren, MI 48387, USA Keywords: nanostructured materials, lithium ion batteries , cathode...2014 to 00-00-2015 4. TITLE AND SUBTITLE High Performance Pillared Vanadium Oxide Cathode for Lithium Ion Batteries 5a. CONTRACT NUMBER 5b. GRANT

  1. Solid contact ion selective electrodes based on carbon nanotubes

    OpenAIRE

    Crespo Paravano, Gastón Adrián

    2010-01-01

    El principal objetivo de esta tesis es el desarrollo de electrodos selectivos de iones de contacto sólido, ESIs-CS, utilizando como capa transductora una red compuesta de nanotubos de carbono.Los electrodos potenciométricos selectivos de iones han sido utilizados en aplicaciones analíticas desde comienzos de 1900. La determinación de pH mediante electrodos de vidrio selectivo de iones fue el primer ESI desarrollado. Hoy en día, el electrodo de vidrio para la determinación de pH es todavía uno...

  2. 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.

  3. Aluminium and hydrogen ions inhibit a mechanosensory calcium-selective cation channel

    Science.gov (United States)

    Ding, J. P.; Pickard, B. G.

    1993-01-01

    The tension-dependent activity of mechanosensory calcium-selective cation channels in excised plasmalemmal patches from onion bulb scale epidermis is modulated by pH in the physiologically meaningful range between 4.5 and 7.2. It is rapidly lowered by lowering pH and rapidly raised by raising pH. Channel activity is effectively inhibited by low levels of aluminium ions and activity can be partially restored by washing for a few minutes. We suggest that under normal conditions the sensitivity of the mechanosensory channels to pH of the wall free space plays important roles in regulation of plant activities such as growth. We further suggest that, when levels of acid and aluminium ions in the soil solution are high, they might inhibit similar sensory channels in cells of the root tip, thus contributing critically to the acid soil syndrome.

  4. Novel optical selective chromone Schiff base chemosensor for Al{sup 3+} ion

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Chun-jiao; Yang, Zheng-yin, E-mail: yangzy@lzu.edu.cn; Fan, Long; Jin, Xiu-long; An, Jun-mei; Cheng, Xiao-ying; Wang, Bao-dui

    2015-02-15

    A novel Schiff-base fluorescent sensor 7-methoxychromone-3-carbaldehyde-((2′-Benzothiazolylthio)-acetyl) hydrazone (MCAH) was synthesized. The new chemosensor possesses dual PET processes simultaneously introducing by both nitrogen and sulfur donors. Upon binding Al{sup 3+}, a significant fluorescence enhancement with a turn-on ratio over 500-fold was triggered. The detection limit of MCAH for Al{sup 3+} was 3.19×10{sup −8} M. - Highlights: • A novel chemosensor based on multiple PET processes was synthesized by a facile one-step reaction. • The sensor exhibits higher sensitivity for Al{sup 3+} than other metal ions with the detection limit reaching at 10{sup −8} M level in ethanol. • The probe exhibited high selectivity for Al{sup 3+} over other metal ions with 500-fold fluorescence enhancement.

  5. Single ion induced surface nanostructures: a comparison between slow highly charged and swift heavy ions.

    Science.gov (United States)

    Aumayr, Friedrich; Facsko, Stefan; El-Said, Ayman S; Trautmann, Christina; Schleberger, Marika

    2011-10-05

    This topical review focuses on recent advances in the understanding of the formation of surface nanostructures, an intriguing phenomenon in ion-surface interaction due to the impact of individual ions. In many solid targets, swift heavy ions produce narrow cylindrical tracks accompanied by the formation of a surface nanostructure. More recently, a similar nanometric surface effect has been revealed for the impact of individual, very slow but highly charged ions. While swift ions transfer their large kinetic energy to the target via ionization and electronic excitation processes (electronic stopping), slow highly charged ions produce surface structures due to potential energy deposited at the top surface layers. Despite the differences in primary excitation, the similarity between the nanostructures is striking and strongly points to a common mechanism related to the energy transfer from the electronic to the lattice system of the target. A comparison of surface structures induced by swift heavy ions and slow highly charged ions provides a valuable insight to better understand the formation mechanisms. © 2011 IOP Publishing Ltd

  6. In Vitro Selection of a DNAzyme Cooperatively Binding Two Lanthanide Ions for RNA Cleavage.

    Science.gov (United States)

    Huang, Po-Jung Jimmy; Vazin, Mahsa; Liu, Juewen

    2016-05-03

    Trivalent lanthanide ions (Ln(3+)) were recently employed to select RNA-cleaving DNAzymes, and three new DNAzymes have been reported so far. In this work, dysprosium (Dy(3+)) was used with a library containing 50 random nucleotides. After six rounds of in vitro selection, a new DNAzyme named Dy10a was obtained and characterized. Dy10a has a bulged hairpin structure cleaving a RNA/DNA chimeric substrate. Dy10a is highly active in the presence of the five Ln(3+) ions in the middle of the lanthanide series (Sm(3+), Eu(3+), Gd(3+), Tb(3+), and Dy(3+)), while its activity descends on the two sides. The cleavage rate reaches 0.6 min(-1) at pH 6 with just 200 nM Sm(3+), which is the fastest among all known Ln(3+)-dependent enzymes. Dy10a binds two Ln(3+) ions cooperatively. When a phosphorothioate (PS) modification is introduced at the cleavage junction, the activity decreases by >2500-fold for both the Rp and Sp diastereomers, and thiophilic Cd(2+) cannot rescue the activity. The pH-rate profile has a slope of 0.37 between pH 4.2 and 5.2, and the slope was even lower at higher pH. On the basis of these data, a model of metal binding is proposed. Finally, a catalytic beacon sensor that can detect Ho(3+) down to 1.7 nM is constructed.

  7. Subcellular carrier-based optical ion-selective nanosensors

    Directory of Open Access Journals (Sweden)

    Susana eCarregal Romero

    2012-04-01

    Full Text Available In this review we discuss two systems based on nanotechnology for real-time sensing of biologically relevant analytes (ions or other biological molecules inside cells in a non-invasive way.

  8. 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.

  9. 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+}.

  10. Influence of Ionic Liquids on the Selectivity of Ion Exchange-Based Polymer Membrane Sensing Layers.

    Science.gov (United States)

    Mendecki, Lukasz; Callan, Nicole; Ahern, Meghan; Schazmann, Benjamin; Radu, Aleksandar

    2016-07-16

    The applicability of ion exchange membranes is mainly defined by their permselectivity towards specific ions. For instance, the needed selectivity can be sought by modifying some of the components required for the preparation of such membranes. In this study, a new class of materials -trihexyl(tetradecyl)phosphonium based ionic liquids (ILs) were used to modify the properties of ion exchange membranes. We determined selectivity coefficients for iodide as model ion utilizing six phosphonium-based ILs and compared the selectivity with two classical plasticizers. The dielectric properties of membranes plasticized with ionic liquids and their response characteristics towards ten different anions were investigated using potentiometric and impedance measurements. In this large set of data, deviations of obtained selectivity coefficients from the well-established Hofmeister series were observed on many occasions thus indicating a multitude of applications for these ion-exchanging systems.

  11. Ion implantation in compound semiconductors for high-performance electronic devices

    Energy Technology Data Exchange (ETDEWEB)

    Zolper, J.C.; Baca, A.G.; Sherwin, M.E.; Klem, J.F.

    1996-05-01

    Advanced electronic devices based on compound semiconductors often make use of selective area ion implantation doping or isolation. The implantation processing becomes more complex as the device dimensions are reduced and more complex material systems are employed. The authors review several applications of ion implantation to high performance junction field effect transistors (JFETs) and heterostructure field effect transistors (HFETs) that are based on compound semiconductors, including: GaAs, AlGaAs, InGaP, and AlGaSb.

  12. Ion aggregation in high salt solutions. VI. Spectral graph analysis of chaotropic ion aggregates

    Science.gov (United States)

    Choi, Jun-Ho; Cho, Minhaeng

    2016-11-01

    Carrying out molecular dynamics simulations and graph theoretical analyses of high salt solutions, and comparing numerically calculated vibrational spectroscopic properties of water with femtosecond IR pump-probe experimental data, we have recently found that ions in high salt solutions can form two morphologically different ion aggregate structures. In the cases of NaCl solutions, Na+ and Cl- tend to form compact cluster-like ion aggregate in high NaCl solutions. In contrast, K+ and SCN- form spatially extended network-like ion aggregates that also exhibit a percolating network behavior. Interestingly, a variety of graph theoretical properties of ion network in high KSCN solutions were found to be very similar to those of water H-bonding network. It was shown that spatially extended ion networks in high KSCN solutions are completely intertwined with water H-bonding networks, which might be the key to understand the high solubility of thiocyanate salts in water. Here, we further consider two salts that have been extensively studied experimentally by using femtosecond IR pump-probe technique, which are NaClO4 and NaBF4. Note that ClO4 - and BF4 - are well-known chaotropic ions that have been believed to behave as water structure breaker. To understand how such chaotropic ions affect water H-bonding structure, we carried out spectral graph analyses of molecular dynamics simulation data of these aqueous solutions. Graph spectra and degree distribution of ion aggregates formed in high NaBF4 and NaClO4 solutions show that these chaotropic anions also have a strong propensity to form ion networks. The fact that salts containing chaotropic ions like SCN-, BF4 - , and ClO4 - have very high solubility limits in water could then be related to our observation that these chaotropic anions with counter cations in high salt solutions are capable of forming intricate ion networks intertwined with water H-bonding networks. We anticipate that the present graph theoretical analysis

  13. SAFT Li-ion Technology for High Rate Applications

    National Research Council Canada - National Science Library

    Nechev, Kamen; Deveney, Bridget; Guseynov, Teymur; Erbacher, John; Vukson, Stephen

    2006-01-01

    SAFT will present an update of its state-of-the art Very High Power (VHP) Lithium-ion (Li-ion) technology. The VHP cells are currently being qualified for use in military aircraft applications as well as in future military hybrid vehicles...

  14. High-discharge-rate lithium ion battery

    Science.gov (United States)

    Liu, Gao; Battaglia, Vincent S; Zheng, Honghe

    2014-04-22

    The present invention provides for a lithium ion battery and process for creating such, comprising higher binder to carbon conductor ratios than presently used in the industry. The battery is characterized by much lower interfacial resistances at the anode and cathode as a result of initially mixing a carbon conductor with a binder, then with the active material. Further improvements in cycleability can also be realized by first mixing the carbon conductor with the active material first and then adding the binder.

  15. Characterization of structure and function of ZS-9, a K+ selective ion trap.

    Directory of Open Access Journals (Sweden)

    Fiona Stavros

    Full Text Available Hyperkalemia, a condition in which serum potassium ions (K+ exceed 5.0 mmol/L, is a common electrolyte disorder associated with substantial morbidity. Current methods of managing hyperkalemia, including organic polymer resins such as sodium polystyrene sulfonate (SPS, are poorly tolerated and/or not effective. Sodium zirconium cyclosilicate (ZS-9 is under clinical development as an orally administered, non-absorbed, novel, inorganic microporous zirconium silicate compound that selectively removes excess K+ in vivo. The development, structure and ion exchange properties of ZS-9 and its hypothesized mechanism of action are described. Based on calculation of the interatomic distances between the atoms forming the ZS-9 micropores, the size of the pore opening was determined to be ∼ 3 Å (∼ diameter of unhydrated K+. Unlike nonspecific organic polymer resins like SPS, the ZS-9 K+ exchange capacity (KEC was unaffected by the presence of calcium (Ca2+ or magnesium ions (Mg2+ and showed>25-fold selectivity for K+ over either Ca2+ or Mg2+. Conversely, the selectivity of SPS for K+ was only 0.2-0.3 times its selectivity for Ca2+ or Mg2+in mixed ionic media. It is hypothesized that the high K+ specificity of ZS-9 is attributable to the chemical composition and diameter of the micropores, which possibly act in an analogous manner to the selectivity filter utilized by physiologic K+ channels. This hypothesized mechanism of action is supported by the multi-ion exchange studies. The effect of pH on the KEC of ZS-9 was tested in different media buffered to mimic different portions of the human gastrointestinal tract. Rapid K+ uptake was observed within 5 minutes - mainly in the simulated small intestinal and large intestinal fluids, an effect that was sustained for up to 1 hour. If approved, ZS-9 will represent a novel, first-in-class therapy for hyperkalemia with improved capacity, selectivity, and speed for entrapping K+ when compared to currently

  16. Selective Permeability of Uranyl Peroxide Nanocages to Different Alkali Ions: Influences from Surface Pores and Hydration Shells

    Energy Technology Data Exchange (ETDEWEB)

    Gao, Yunyi; Haso, Fadi; Szymanowski, Jennifer E. S.; Zhou, Jing; Hu, Lang; Burns, Peter C.; Liu, Tianbo

    2015-11-16

    The precise guidance to different ions across the biological channels is essential for many biological processes. An artificial nanopore system will facilitate the study of the ion-transport mechanism through nanosized channels and offer new views for designing nanodevices. Herein we reveal that a 2.5 nm-sized, fullerene-shaped molecular cluster Li48+mK12(OH)m[UO2(O2)(OH)]60-(H2O)n (m≈20 and n≈310) (U60) shows selective permeability to different alkali ions. The subnanometer pores on the water–ligand-rich surface of U60 are able to block Rb+ and Cs+ ions from passing through, while allowing Na+ and K+ ions, which possess larger hydrated sizes, to enter the interior space of U60. An interestingly high entropy gain during the binding process between U60 and alkali ions suggests that the hydration shells of Na+/K+ and U60 are damaged during the interaction. The ion selectivity of U60 is greatly influenced by both the morphologies of the surface nanopores and the dynamics of the hydration shells.

  17. Selective permeability of uranyl peroxide nanocages to different alkali ions: influences from surface pores and hydration shells

    Energy Technology Data Exchange (ETDEWEB)

    Gao, Yunyi; Haso, Fadi; Zhou, Jing; Hu, Lang; Liu, Tianbo [Department of Polymer Science, University of Akron, OH (United States); Szymanowski, Jennifer E.S.; Burns, Peter C. [Department of Civil Engineering and Geological Sciences, University of Notre Dame, IN (United States)

    2015-12-14

    The precise guidance to different ions across the biological channels is essential for many biological processes. An artificial nanopore system will facilitate the study of the ion-transport mechanism through nanosized channels and offer new views for designing nanodevices. Herein we reveal that a 2.5 nm-sized, fullerene-shaped molecular cluster Li{sub 48+m}K{sub 12}(OH){sub m}[UO{sub 2}(O{sub 2})(OH)]{sub 60-}(H{sub 2}O){sub n} (m∼20 and n∼310) (U{sub 60}) shows selective permeability to different alkali ions. The subnanometer pores on the water-ligand-rich surface of U{sub 60} are able to block Rb{sup +} and Cs{sup +} ions from passing through, while allowing Na{sup +} and K{sup +} ions, which possess larger hydrated sizes, to enter the interior space of U{sub 60}. An interestingly high entropy gain during the binding process between U{sub 60} and alkali ions suggests that the hydration shells of Na{sup +}/K{sup +} and U{sub 60} are damaged during the interaction. The ion selectivity of U{sub 60} is greatly influenced by both the morphologies of the surface nanopores and the dynamics of the hydration shells. (copyright 2015 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  18. Development of in situ ion selective sensors for dissolution

    Energy Technology Data Exchange (ETDEWEB)

    Bohets, Hugo [Antwerp University, Chemistry Department, Groenenborgerlaan 171, B-2020 Antwerpen (Belgium); Vanhoutte, Koen [Johnson and Johnson Pharmaceutical Research and Development, Turnhoutseweg 30, B-2340 Beerse (Belgium); De Maesschalck, Roy [Johnson and Johnson Pharmaceutical Research and Development, Turnhoutseweg 30, B-2340 Beerse (Belgium); Cockaerts, Paul [Johnson and Johnson Pharmaceutical Research and Development, Turnhoutseweg 30, B-2340 Beerse (Belgium); Vissers, Bert [Antwerp University, Chemistry Department, Groenenborgerlaan 171, B-2020 Antwerpen (Belgium); Nagels, Luc J. [Antwerp University, Chemistry Department, Groenenborgerlaan 171, B-2020 Antwerpen (Belgium)]. E-mail: luc.nagels@ua.ac.be

    2007-01-02

    The dissolution of formulations of the drugs dapoxetine, paliperidone, cinnarizine, tetrazepam, mebeverine, loperamide, galantamine and ibuprofen was studied by an in-line potentiometric measurement system. The transpose of a Nikolskii-Eisenman type function performed the conversion of potential to percentage of dissolution. A novel gradient membrane electrode was developed especially for dissolution, varying continuously in composition from an ionically conducting rubber phase to an electronically conducting solid state PVC/graphite composite. The gradient part had a thickness of 200 {mu}m. The electrodes life span exceeded 6 months. An ion exchange procedure was used to prepare them for one specific drug. This enabled us to use one universal electrode built to measure a wide array of drugs. The system parameters such as accuracy, reproducibility and linearity were presented with the data obtained for the drug dapoxetine. In dissolution, accurate measurements were possible from 10{sup -9} to 10{sup -3} M concentrations, for high log P drugs. The effect of t {sub 90} response times on the measurement error was estimated. The t {sub 90} response times of the electrodes were concentration dependent, and varied between 50 and 10 s for, respectively, 10{sup -6} and 10{sup -3} M concentrations. Potential drift was studied in detail. The measurements performed with these electrodes showed an accuracy of 1%, and inter- and intra electrode variabilities of 0.6 and 1.7%, respectively. The electrodes were successfully applied in colloidal media containing suspended matter, typically formed during dissolution of tablets. The advantages and pitfalls of potentiometry over the presently used techniques for dissolution testing are discussed.

  19. Intense highly charged ion beam production and operation with a superconducting electron cyclotron resonance ion source

    Directory of Open Access Journals (Sweden)

    H. W. Zhao

    2017-09-01

    Full Text Available The superconducting electron cyclotron resonance ion source with advanced design in Lanzhou (SECRAL is a superconducting-magnet-based electron cyclotron resonance ion source (ECRIS for the production of intense highly charged heavy ion beams. It is one of the best performing ECRISs worldwide and the first superconducting ECRIS built with an innovative magnet to generate a high strength minimum-B field for operation with heating microwaves up to 24–28 GHz. Since its commissioning in 2005, SECRAL has so far produced a good number of continuous wave intensity records of highly charged ion beams, in which recently the beam intensities of ^{40}Ar^{12+} and ^{129}Xe^{26+} have, for the first time, exceeded 1 emA produced by an ion source. Routine operations commenced in 2007 with the Heavy Ion accelerator Research Facility in Lanzhou (HIRFL, China. Up to June 2017, SECRAL has been providing more than 28,000 hours of highly charged heavy ion beams to the accelerator demonstrating its great capability and reliability. The great achievement of SECRAL is accumulation of numerous technical advancements, such as an innovative magnetic system and an efficient double-frequency (24+18  GHz heating with improved plasma stability. This article reviews the development of SECRAL and production of intense highly charged ion beams by SECRAL focusing on its unique magnet design, source commissioning, performance studies and enhancements, beam quality and long-term operation. SECRAL development and its performance studies representatively reflect the achievements and status of the present ECR ion source, as well as the ECRIS impacts on HIRFL.

  20. Intense highly charged ion beam production and operation with a superconducting electron cyclotron resonance ion source

    Science.gov (United States)

    Zhao, H. W.; Sun, L. T.; Guo, J. W.; Lu, W.; Xie, D. Z.; Hitz, D.; Zhang, X. Z.; Yang, Y.

    2017-09-01

    The superconducting electron cyclotron resonance ion source with advanced design in Lanzhou (SECRAL) is a superconducting-magnet-based electron cyclotron resonance ion source (ECRIS) for the production of intense highly charged heavy ion beams. It is one of the best performing ECRISs worldwide and the first superconducting ECRIS built with an innovative magnet to generate a high strength minimum-B field for operation with heating microwaves up to 24-28 GHz. Since its commissioning in 2005, SECRAL has so far produced a good number of continuous wave intensity records of highly charged ion beams, in which recently the beam intensities of 40Ar+ and 129Xe26+ have, for the first time, exceeded 1 emA produced by an ion source. Routine operations commenced in 2007 with the Heavy Ion accelerator Research Facility in Lanzhou (HIRFL), China. Up to June 2017, SECRAL has been providing more than 28,000 hours of highly charged heavy ion beams to the accelerator demonstrating its great capability and reliability. The great achievement of SECRAL is accumulation of numerous technical advancements, such as an innovative magnetic system and an efficient double-frequency (24 +18 GHz ) heating with improved plasma stability. This article reviews the development of SECRAL and production of intense highly charged ion beams by SECRAL focusing on its unique magnet design, source commissioning, performance studies and enhancements, beam quality and long-term operation. SECRAL development and its performance studies representatively reflect the achievements and status of the present ECR ion source, as well as the ECRIS impacts on HIRFL.

  1. High Energy Ion Acceleration by Extreme Laser Radiation Pressure

    Science.gov (United States)

    2017-03-14

    AFRL-AFOSR-UK-TR-2017-0015 High energy ion acceleration by extreme laser radiation pressure Paul McKenna UNIVERSITY OF STRATHCLYDE VIZ ROYAL COLLEGE...MM-YYYY)   14-03-2017 2. REPORT TYPE  Final 3. DATES COVERED (From - To)  01 May 2013 to 31 Dec 2016 4. TITLE AND SUBTITLE High energy ion acceleration...Prescribed by ANSI Std. Z39.18 Page 1 of 1FORM SF 298 3/15/2017https://livelink.ebs.afrl.af.mil/livelink/llisapi.dll 1 HIGH ENERGY ION ACCELERATION BY

  2. Proton and Ion Sources for High Intensity Accelerators

    CERN Multimedia

    Scrivens, R

    2004-01-01

    Future high intensity ion accelerators, including the Spallation Neutron Source (SNS), the European Spallation Source (ESS), the Superconducting Proton Linac (SPL) etc, will require high current and high duty factor sources for protons and negative hydrogen ions. In order to achieve these goals, a comparison of the Electron Cyclotron Resonance, radio-frequency and Penning ion sources, among others, will be made. For each of these source types, the present operational sources will be compared to the state-of-the-art research devices with special attention given to reliability and availability. Finally, the future research and development aims will be discussed.

  3. Multi-energy ion implantation from high-intensity laser

    OpenAIRE

    Cutroneo Mariapompea; Torrisi Lorenzo; Ullschmied Jiri; Dudzak Roman

    2016-01-01

    The laser-matter interaction using nominal laser intensity above 1015 W/cm2 generates in vacuum non-equilibrium plasmas accelerating ions at energies from tens keV up to hundreds MeV. From thin targets, using the TNSA regime, plasma is generated in the forward direction accelerating ions above 1 MeV per charge state and inducing high-ionization states. Generally, the ion energies follow a Boltzmann-like distribution characterized by a cutoff at high energy and by a Coulomb-shift towards high ...

  4. Miniaturized, Planar Ion-selective Electrodes Fabricated by Means of Thick-film Technology

    Directory of Open Access Journals (Sweden)

    Robert Koncki

    2006-04-01

    Full Text Available Various planar technologies are employed for developing solid-state sensorshaving low cost, small size and high reproducibility; thin- and thick-film technologies aremost suitable for such productions. Screen-printing is especially suitable due to itssimplicity, low-cost, high reproducibility and efficiency in large-scale production. Thistechnology enables the deposition of a thick layer and allows precise pattern control.Moreover, this is a highly economic technology, saving large amounts of the used inks. Inthe course of repetitions of the film-deposition procedure there is no waste of material dueto additivity of this thick-film technology. Finally, the thick films can be easily and quicklydeposited on inexpensive substrates. In this contribution, thick-film ion-selective electrodesbased on ionophores as well as crystalline ion-selective materials dedicated forpotentiometric measurements are demonstrated. Analytical parameters of these sensors arecomparable with those reported for conventional potentiometric electrodes. All mentionedthick-film strip electrodes have been totally fabricated in only one, fully automated thick-film technology, without any additional manual, chemical or electrochemical steps. In allcases simple, inexpensive, commercially available materials, i.e. flexible, plastic substratesand easily cured polymer-based pastes were used.

  5. Atomic physics with highly charged ions. Progress report

    Energy Technology Data Exchange (ETDEWEB)

    Richard, P.

    1994-08-01

    The study of inelastic collision phenomena with highly charged projectile ions and the interpretation of spectral features resulting from these collisions remain as the major focal points in the atomic physics research at the J.R. Macdonald Laboratory, Kansas State University, Manhattan, Kansas. The title of the research project, ``Atomic Physics with Highly Charged Ions,`` speaks to these points. The experimental work in the past few years has divided into collisions at high velocity using the primary beams from the tandem and LINAC accelerators and collisions at low velocity using the CRYEBIS facility. Theoretical calculations have been performed to accurately describe inelastic scattering processes of the one-electron and many-electron type, and to accurately predict atomic transition energies and intensities for x rays and Auger electrons. Brief research summaries are given for the following: (1) electron production in ion-atom collisions; (2) role of electron-electron interactions in two-electron processes; (3) multi-electron processes; (4) collisions with excited, aligned, Rydberg targets; (5) ion-ion collisions; (6) ion-molecule collisions; (7) ion-atom collision theory; and (8) ion-surface interactions.

  6. Harvesting polysulfides by sealing the sulfur electrode in a composite ion-selective net

    Science.gov (United States)

    Chen, Yazhou; Li, Zhong; Li, Xuekui; Zeng, Danli; Xu, Guodong; Zhang, Yunfeng; Sun, Yubao; Ke, Hanzhong; Cheng, Hansong

    2017-11-01

    A cathode was prepared by sealing a carbon supported sulfur electrode inside a composite ion-selective net made of carbon, binder and lithiated ionomer to restrict shuttling of polysulfide anionic species. As a result, the soluble polysulfide anions become unable to escape from the composite ion-selective films due to the electrostatic repulsion between the immobilized single ion conducting ionomers and the polysulfides with no dead angles. Experimentally, lithiated 4,4‧-difluoro bis(benzene sulfonyl)imide and PEG200 were copolymerized to form a polyether based single ion conducting polymer. The ionic conductivity of the blend film made of ionomer and poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) at a mass ratio of 1:1 is 0.57 mS cm-1 at room temperature. The battery capacity with the sealed sulfur electrode is 1412 mAh g-1 at 0.5 C, 1041 mAh g-1 at 1.0 C, 873 mAh g-1 at 2.0 C and 614 mAh g-1 at 5.0 C, significantly better than the results with lithiated Nafion especially at high C rates. In addition, a long cycling test at 2 C for 500 cycles gives rise to a stable capacity of 800 mAh g-1. The intrinsic electrostatic repulsion between polysulfide anions and the negatively charged electrolyte film, together with the overall sealed electrode configuration, is responsible for blocking the shuttling of polysulfides effectively.

  7. Expression and purification of native and functional influenza A virus matrix 2 proton selective ion channel.

    Science.gov (United States)

    Desuzinges Mandon, Elodie; Traversier, Aurélien; Champagne, Anne; Benier, Lorraine; Audebert, Stéphane; Balme, Sébastien; Dejean, Emmanuel; Rosa Calatrava, Manuel; Jawhari, Anass

    2017-03-01

    Influenza A virus displays one of the highest infection rates of all human viruses and therefore represents a severe human health threat associated with an important economical challenge. Influenza matrix protein 2 (M2) is a membrane protein of the viral envelope that forms a proton selective ion channel. Here we report the expression and native isolation of full length active M2 without mutations or fusions. The ability of the influenza virus to efficiently infect MDCK cells was used to express native M2 protein. Using a Calixarene detergents/surfactants based approach; we were able to solubilize most of M2 from the plasma membrane and purify it. The tetrameric form of native M2 was maintained during the protein preparation. Mass spectrometry shows that M2 was phosphorylated in its cytoplasmic tail (serine 64) and newly identifies an acetylation of the highly conserved Lysine 60. ELISA shows that solubilized and purified M2 was specifically recognized by M2 antibody MAB65 and was able to displace the antibody from M2 MDCK membranes. Using a bilayer voltage clamp measurement assay, we demonstrate a pH dependent proton selective ion channel activity. The addition of the M2 ion channel blocker amantadine allows a total inhibition of the channel activity, illustrating therefore the specificity of purified M2 activity. Taken together, this work shows the production and isolation of a tetrameric and functional native M2 ion channel that will pave the way to structural and functional characterization of native M2, conformational antibody development, small molecules compounds screening towards vaccine treatment. Copyright © 2016 Elsevier Inc. All rights reserved.

  8. High-resolution excitation of ions in a low-pressure linear ion trap.

    Science.gov (United States)

    Collings, B A

    2011-01-15

    An exploration of the parameters necessary to obtain high-resolution excitation, using dipolar excitation, of an ion in a linear ion trap has been undertaken in this study. These parameters included ion trap pressure, excitation amplitude, excitation period, drive frequency of the ion trap, Mathieu q value and the mass of the ion of interest. An understanding of how these parameters play a role in high-resolution excitation is necessary to the development of a method for the targeted tandem mass spectrometric (MS/MS) analysis of ions with the same nominal mass. Resonance excitation profiles with full width half maxima as narrow as 0.015 m/z units could be obtained, under the right conditions, for an ion from a homogenously substituted triazatriphosphorine at m/z 322.049, which translates into a mass resolution of >21 500. In this particular case the requirement for high resolution was a low trap pressure (3.8 × 10(-5) Torr), low excitation amplitude (3 mV), long excitation period (100 ms) and a high Mathieu q value(0.8) when using a drive frequency of 1.228 MHz. Similar conditions were used to demonstrate the isolation of individual [M + H](+) component ions from mixtures of bromazepam (m/z 316.008)/chlorprothixene (m/z 316.0921)/fendiline (m/z 316.206) and chlorprothixene (m/z 316.0921)/oxycodone (m/z 316.1543)/fendiline (m/z 316.206) prior to obtaining product ion spectra with excitation at q = 0.236. In the former mixture the individual components were isolated with near 100% efficiency while in the latter mixture the isolation efficiency dropped to near 50% for the oxycodone component and to 80% for the other components. Copyright © 2010 John Wiley & Sons, Ltd.

  9. Ion-Specific Nutrient Management in Closed Systems: The Necessity for Ion-Selective Sensors in Terrestrial and Space-Based Agriculture and Water Management Systems

    Science.gov (United States)

    Bamsey, Matthew; Graham, Thomas; Thompson, Cody; Berinstain, Alain; Scott, Alan; Dixon, Michael

    2012-01-01

    The ability to monitor and control plant nutrient ions in fertigation solutions, on an ion-specific basis, is critical to the future of controlled environment agriculture crop production, be it in traditional terrestrial settings (e.g., greenhouse crop production) or as a component of bioregenerative life support systems for long duration space exploration. Several technologies are currently available that can provide the required measurement of ion-specific activities in solution. The greenhouse sector has invested in research examining the potential of a number of these technologies to meet the industry's demanding requirements, and although no ideal solution yet exists for on-line measurement, growers do utilize technologies such as high-performance liquid chromatography to provide off-line measurements. An analogous situation exists on the International Space Station where, technological solutions are sought, but currently on-orbit water quality monitoring is considerably restricted. This paper examines the specific advantages that on-line ion-selective sensors could provide to plant production systems both terrestrially and when utilized in space-based biological life support systems and how similar technologies could be applied to nominal on-orbit water quality monitoring. A historical development and technical review of the various ion-selective monitoring technologies is provided. PMID:23201999

  10. Ion-Specific Nutrient Management in Closed Systems: The Necessity for Ion-Selective Sensors in Terrestrial and Space-Based Agriculture and Water Management Systems

    Directory of Open Access Journals (Sweden)

    Alain Berinstain

    2012-10-01

    Full Text Available The ability to monitor and control plant nutrient ions in fertigation solutions, on an ion-specific basis, is critical to the future of controlled environment agriculture crop production, be it in traditional terrestrial settings (e.g., greenhouse crop production or as a component of bioregenerative life support systems for long duration space exploration. Several technologies are currently available that can provide the required measurement of ion-specific activities in solution. The greenhouse sector has invested in research examining the potential of a number of these technologies to meet the industry’s demanding requirements, and although no ideal solution yet exists for on-line measurement, growers do utilize technologies such as high-performance liquid chromatography to provide off-line measurements. An analogous situation exists on the International Space Station where, technological solutions are sought, but currently on-orbit water quality monitoring is considerably restricted. This paper examines the specific advantages that on-line ion-selective sensors could provide to plant production systems both terrestrially and when utilized in space-based biological life support systems and how similar technologies could be applied to nominal on-orbit water quality monitoring. A historical development and technical review of the various ion-selective monitoring technologies is provided.

  11. High voltage and high specific capacity dual intercalating electrode Li-ion batteries

    Science.gov (United States)

    West, William C. (Inventor); Blanco, Mario (Inventor)

    2010-01-01

    The present invention provides high capacity and high voltage Li-ion batteries that have a carbonaceous cathode and a nonaqueous electrolyte solution comprising LiF salt and an anion receptor that binds the fluoride ion. The batteries can comprise dual intercalating electrode Li ion batteries. Methods of the present invention use a cathode and electrode pair, wherein each of the electrodes reversibly intercalate ions provided by a LiF salt to make a high voltage and high specific capacity dual intercalating electrode Li-ion battery. The present methods and systems provide high-capacity batteries particularly useful in powering devices where minimizing battery mass is important.

  12. 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.

  13. Mechanism study of selective heavy metal ion removal with polypyrrole-functionalized polyacrylonitrile nanofiber mats

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Jianqiang; Luo, Chao [Key Laboratory of Carbon Fiber and Functional Polymers, Ministry of Education, Beijing University of Chemical Technology, Beijing 100029 (China); Qi, Genggeng [Department of Materials Science and Engineering, Cornell University, Ithaca, NY (United States); Pan, Kai, E-mail: pankai@mail.buct.edu.cn [Key Laboratory of Carbon Fiber and Functional Polymers, Ministry of Education, Beijing University of Chemical Technology, Beijing 100029 (China); Department of Materials Science and Engineering, Cornell University, Ithaca, NY (United States); Cao, Bing, E-mail: bcao@mail.buct.edu.cn [Key Laboratory of Carbon Fiber and Functional Polymers, Ministry of Education, Beijing University of Chemical Technology, Beijing 100029 (China)

    2014-10-15

    Graphical abstract: - Highlights: • PAN/PPy core/shell nanofiber used for Cr(VI) removal. • Adsorption mechanisms were investigated. • Selective adsorption performances were investigated. - Abstract: Polyacrylonitrile/polypyrrole (PAN/PPy) core/shell nanofiber mat was prepared through electrospinning followed by a simple chemical oxidation method. The polypyrrole-functionalized nanofiber mats showed selective adsorption performance for anions. The interaction between heavy metal anions and polypyrrole (especially the interaction between Cr{sub 2}O{sub 7}{sup 2−} and polypyrrole) during the adsorption process was studied. The results showed that the adsorption process included two steps: one was the anion exchange process between the Cl{sup −} and Cr(VI), and the other was the redox process for the Cr(VI) ions. The adsorption amount was related to the protonation time of the PAN/PPy nanofiber mat and increased as protonation time increased. Meanwhile, the Cr(VI) ions were reduced to Cr(III) through the reaction with amino groups of polypyrrole (from secondary amines to tertiary amines). PAN/PPy nanofiber mat showed high selectivity for Cr(VI), and the adsorption performance was nearly unaffected by other co-existing anions (Cl{sup −}, NO{sub 3}{sup −}, and SO{sub 4}{sup 2−}) except for PO{sub 4}{sup 3−} for the pH change.

  14. A new rhodamine based 'turn-on'Cu²⁺ ion selective chemosensor in ...

    Indian Academy of Sciences (India)

    ... to Cu²⁺ ion-assisted hydrolysis followed by spirolactam ring opening of the probe (L) in 20mM HEPES buffer [pH 7.4; water/acetonitrile (9:1 v/v)]. The competitive ions do not affect the selectivity and specificity of the probe (L) in the detection of Cu²⁺ ions. The cell imaging study using fluorescence microscope showed that ...

  15. High-Voltage, High-Impedance Ion Beam Production

    Science.gov (United States)

    2009-06-01

    collaboration with Tim Renk and Victor Harper- Slaboszewicz of Sandia National Laboratories. Joint experiments on Mercury are planned for the future...Young, "Pinched-Beam Ion Diode Scaling on the Aurora Pulser," J. Appl. Phys. 53, 8543 (1982). [8] T. J. Renk , et al., "Generation of Ion Beams in

  16. Ion aggregation in high salt solutions. II. Spectral graph analysis of water hydrogen-bonding network and ion aggregate structures

    Science.gov (United States)

    Choi, Jun-Ho; Cho, Minhaeng

    2014-10-01

    Graph theory in mathematics and computer science is the study of graphs that are structures with pairwise connections between any objects. Here, the spectral graph theory and molecular dynamics simulation method are used to describe both morphological variation of ion aggregates in high salt solutions and ion effects on water hydrogen-bonding network structure. From the characteristic value analysis of the adjacency matrices that are graph theoretical representations of ion clusters, ion networks, and water H-bond structures, we obtained the ensemble average eigenvalue spectra revealing intricate connectivity and topology of ion aggregate structure that can be classified as either ion cluster or ion network. We further show that there is an isospectral relationship between the eigenvalue spectra of ion networks in high KSCN solutions and those of water H-bonding networks. This reveals the isomorphic relationship between water H-bond structure and ion-ion network structure in KSCN solution. On the other hand, the ion clusters formed in high NaCl solutions are shown to be graph-theoretically and morphologically different from the ion network structures in KSCN solutions. These observations support the bifurcation hypothesis on large ion aggregate growth mechanism via either ion cluster or ion network formation. We thus anticipate that the present spectral graph analyses of ion aggregate structures and their effects on water H-bonding network structures in high salt solutions can provide important information on the specific ion effects on water structures and possibly protein stability resulting from protein-water interactions.

  17. Ion aggregation in high salt solutions. II. Spectral graph analysis of water hydrogen-bonding network and ion aggregate structures.

    Science.gov (United States)

    Choi, Jun-Ho; Cho, Minhaeng

    2014-10-21

    Graph theory in mathematics and computer science is the study of graphs that are structures with pairwise connections between any objects. Here, the spectral graph theory and molecular dynamics simulation method are used to describe both morphological variation of ion aggregates in high salt solutions and ion effects on water hydrogen-bonding network structure. From the characteristic value analysis of the adjacency matrices that are graph theoretical representations of ion clusters, ion networks, and water H-bond structures, we obtained the ensemble average eigenvalue spectra revealing intricate connectivity and topology of ion aggregate structure that can be classified as either ion cluster or ion network. We further show that there is an isospectral relationship between the eigenvalue spectra of ion networks in high KSCN solutions and those of water H-bonding networks. This reveals the isomorphic relationship between water H-bond structure and ion-ion network structure in KSCN solution. On the other hand, the ion clusters formed in high NaCl solutions are shown to be graph-theoretically and morphologically different from the ion network structures in KSCN solutions. These observations support the bifurcation hypothesis on large ion aggregate growth mechanism via either ion cluster or ion network formation. We thus anticipate that the present spectral graph analyses of ion aggregate structures and their effects on water H-bonding network structures in high salt solutions can provide important information on the specific ion effects on water structures and possibly protein stability resulting from protein-water interactions.

  18. Development of a laser ion source for production of high-intensity heavy-ion beams

    Science.gov (United States)

    Kashiwagi, H.; Yamada, K.; Kurashima, S.

    2017-09-01

    A laser ion source has been developed as a high-intensity source for the ion implanter and the single pulsed beam of the azimuthally varying field cyclotron at TIARA. Highly charged beams of C5+ and C6+ ions and low-charged beams of heavy ions such as C, Al, Ti, Cu, Au, and Pt are required for the single-pulse acceleration in the cyclotron and for the ion implanter, respectively. In the vacuum chamber of the ion source, a target holder on a three-dimensional linear-motion stage provides a fresh surface for each laser shot. A large-sized target with a maximum size of 300 mm × 135 mm is mounted on the holder for long-term operation. The ion current (ion charge flux) in the laser-produced plasma is measured by a Faraday cup and time-of-flight spectra of each charge state are measured using a 90° cylindrical electrostatic analyzer just behind the Faraday cup. Carbon-plasma-generation experiments indicate that the source produces intense high- and low-charged pulsed ion beams. At a laser energy of 483 mJ (2.3 × 1013 W/cm2), average C6+ current of 13 mA and average C5+ current of 23 mA were obtained over the required time duration for single-pulse acceleration in the cyclotron (49 ns for C6+ and 80 ns for C5+). Furthermore, at 45 mJ (2.1 × 1012 W/cm2), an average C2+ current of 1.6 mA over 0.88 μs is obtained.

  19. Wavelength-selective fluorescence in ion channels formed by ...

    Indian Academy of Sciences (India)

    We have previously shown that the tryptophan residues in ion channels formed by the naturally occurring peptide, gramicidin A', display wavelength-dependent fluorescence characteristics due to the motionally restricted environment in which they are localized. In order to check the influence of ground-state heterogeneity in ...

  20. Energy Harvesting from Reverse Electrodialysis in Ion-Selective Membrane Formed with Self-Assembled Nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Choi, Eunpyo; Kwon, Kilsung; Kim, Dajoong; Park, Jungyul [Sogang University, Seoul (Korea, Republic of)

    2014-05-15

    This paper presents a novel microplatform for high power generation based on reverse electrodialysis. The ideal cation-selective membrane for power generation was realized using geometrically controlled in situ self-assembled nanoparticles. Our proposed membranes can be constructed through a simple and cost-effective process that uses microdroplet control with nanoparticles in a microchannel. Another advantage of our system is that the maximum power and energy conversion efficiency can be improved by changing the geometry of the microchannel and proper selection of the nanoparticle size and material. This proposed platform can be used to supply power sources to other microdevices and contribute to a fundamental understanding of ion transport behavior and the power generation mechanism.

  1. Ion-selective electrodes in organic elemental and functional group analysis: a review

    Energy Technology Data Exchange (ETDEWEB)

    Selig, W.

    1977-11-08

    The literature on the use of ion-selective electrodes in organic elemental and functional group analysis is surveyed in some detail. The survey is complete through Chemical Abstracts, Vol. 83 (1975). 40 figures, 52 tables, 236 references.

  2. Preparation of a novel potassium ion imprinted polymeric nanoparticles based on dicyclohexyl 18C6 for selective determination of K{sup +} ion in different water samples

    Energy Technology Data Exchange (ETDEWEB)

    Rajabi, Hamid Reza, E-mail: h.rajabi@mail.yu.ac.ir [Chemistry Department, Yasouj University, Yasouj, 75918-74831 (Iran, Islamic Republic of); Shamsipur, Mojtaba [Department of Chemistry, Razi University, Kermanshah (Iran, Islamic Republic of); Pourmortazavi, Seied Mahdi [Faculty of Material and Manufacturing Technologies, Malek-Ashtar University of Technology, Tehran (Iran, Islamic Republic of)

    2013-08-01

    This work reports the first application of the ion imprinting technology for determination of potassium ion by precipitation polymerization method. Ion imprinted polymeric (IIP) nanoparticles were prepared by using dicyclohexyl 18C6 (DC18C6) as a K{sup +} ion selective crown ether, in the acetonitrile–dimethylsulfoxide (3:1; v/v) mixture as porogen. The imprint potassium ion was removed from the polymeric matrix using 0.5 M HNO{sub 3}. The scanning electron microscopy (SEM) micrographs showed colloidal nanoparticles of 60–90 nm in diameter and slightly irregular in shape. The obtained ion-imprinted particles for K{sup +} showed selective recognition with rapid adsorption and desorption processes. It was found that imprinting results in increased affinity of the material toward K{sup +} ion over other competitor metal ions with the same charge and/or close ionic radius. The synthesized IIP nanobeads were shown to be promising for solid-phase extraction coupled with flame photometry for determination of trace K{sup +} ion in different water samples. Highlights: • Synthesis of nano-sized ion imprinted polymers for separation of potassium ions • Rapid kinetics of adsorption and desorption of K{sup +} ion on the resulting IIPs • First study on application of ion imprinting for detection of K{sup +} based on DC18C6 • An excellent selectivity toward K{sup +} ion over a range of strong competing metal ions.

  3. Ion beams in SEM : An experiment towards a high brightness low energy spread electron impact gas ion source

    NARCIS (Netherlands)

    Jun, D.S.; Kutchoukov, V.G.; Kruit, P.

    2011-01-01

    A next generation ion source suitable for both high resolution focused ion beam milling and imaging applications is currently being developed. The new ion source relies on a method of which positively charged ions are extracted from a miniaturized gas chamber where neutral gas atoms become ionized

  4. Ion source and injection line for high intensity medical cyclotron.

    Science.gov (United States)

    Jia, XianLu; Guan, Fengping; Yao, Hongjuan; Zhang, TianJue; Yang, Jianjun; Song, Guofang; Ge, Tao; Qin, Jiuchang

    2014-02-01

    A 14 MeV high intensity compact cyclotron, CYCIAE-14, was built at China Institute of Atomic Energy (CIAE). An injection system based on the external H- ion source was used on CYCIAE-14 so as to provide high intensity beam, while most positron emission tomography cyclotrons adopt internal ion source. A beam intensity of 100 μA/14 MeV was extracted from the cyclotron with a small multi-cusp H- ion source (CIAE-CH-I type) and a short injection line, which the H- ion source of 3 mA/25 keV H- beam with emittance of 0.3π mm mrad and the injection line of with only 1.2 m from the extraction of ion source to the medial plane of the cyclotron. To increase the extracted beam intensity of the cyclotron, a new ion source (CIAE-CH-II type) of 9.1 mA was used, with maximum of 500 μA was achieved from the cyclotron. The design and test results of the ion source and injection line optimized for high intensity acceleration will be given in this paper.

  5. High Resolution Observations of Escaping Ions in the Martian Magnetotail

    Science.gov (United States)

    Halekas, J. S.; Raman, C.; Brain, D.; DiBraccio, G. A.; Harada, Y.; McFadden, J. P.; Mitchell, D. L.; Connerney, J. E. P.; Jakosky, B. M.

    2016-12-01

    Ions escape from the Martian upper atmosphere via a number of channels, including the central plasmasheet of the magnetotail. Mars Express observations show that the heavy ions O+ and O2+ escaping through the central tail often have approximately the same energy, suggesting acceleration in a quasi-static electric field, which has been interpreted as a Hall electric field. The Solar Wind Ion Analyzer (SWIA) on MAVEN was designed to measure the upstream solar wind. However, during orbit segments with appropriate spacecraft attitude, SWIA can also make high resolution measurements of escaping ions in the tail. During the prime mission, these observations were only returned sporadically, during periods of intense escaping fluxes that fortuitously triggered a mode switch. Now, in the extended mission, we return high resolution observations from SWIA routinely. Some of these high resolution measurements reveal slight differences in both the direction and energy of escaping O+ and O2+ ions, which may help determine the acceleration process(es). We investigate the location and solar wind conditions for which the escaping ions separate in energy and angle and the systematics of their energies and flow vectors, and discuss the implications for ion acceleration and the overall picture of Martian atmospheric escape.

  6. A selective chemosensor for fluoride ion and its interaction with Calf Thymus DNA

    Science.gov (United States)

    Ghosh, Soumen; Al Masum, Abdulla; Ganguly, Aniruddha; Islam, Md. Maidul; Alam, Md. Akhtarul; Guchhait, Nikhil

    2017-05-01

    The amido-Schiff base 1 (N1, N3-bis (2-nitrobenzylidene)benzene-1,3-dicabohydrazide) containing a sbnd CONHsbnd group and sbnd CHdbnd Nsbnd linkage has been synthesized by the condensation between isophthalic acid dihydrazide and o-nitrobenzaldehyde. This molecule can act as a fluoride ion sensor with high selectivity and sensitivity. Presence of nitro group in the phenyl ring may be responsible for the detection of fluoride ion visually with a dramatic color change from colorless to deep red in aqueous dimethyl sulphoxide solution. This Schiff base can be used as test kit for sensing of fluoride ion in the solid state. Compound 1 can detect fluoride also in commercially available toothpaste. As the compound has adequate solubility in DMSO-water mixture (7:93, v/v) and having some hydrogen bond donor and acceptor centers, we have investigated its nature of binding with Calf Thymus-DNA (CT-DNA) using theoretical molecular modelling and other experimental methods like UV-vis spectroscopy, circular dichroic and thermal melting studies. Thermodynamic parameters have been obtained using the well known Van't Hoff's equation. From both theoretical and experimental findings it has been observed that it can interact effectively with CT-DNA with binding energy - 7.55 kcal/mol to - 7.50 kcal/mol.

  7. Quantification of methanol in the presence of ethanol by selected ion flow tube mass spectrometry.

    Science.gov (United States)

    Chambers-Bédard, Catherine; Ross, Brian M

    The quantification of trace compounds in alcoholic beverages is a useful means to both investigate the chemical basis of beverage flavor and to facilitate quality control during the production process. One compound of interest is methanol which, due to it being toxic, must not exceed regulatory limits. The analysis of headspace gases is a desirable means to do this since it does not require direct sampling of the liquid material. One established means to conduct headspace analysis is selected ion flow tube mass spectrometry (SIFT-MS). The high concentration of ethanol present in the headspace of alcoholic drinks complicates the analysis, however, via reacting with the precursor ions central to this technique. We therefore investigated whether methanol could be quantified in the presence of a large excess of ethanol using SIFT-MS. We found that methanol reacted with ionized ethanol to generate product ions that could be used to quantify methanol concentrations and used this technique to quantify methanol in beverages containing different quantities of ethanol. We conclude that SIFT-MS can be used to quantify trace compounds in alcoholic beverages by determining the relevant reaction chemistry.

  8. BILAYER LIPID MEMBRANE (BLM) BASED ION SELECTIVE ELECTRODES AT THE MESO, MICRO, AND NANO SCALES

    OpenAIRE

    Liu, Bingwen; Rieck, Daniel; Van Wie, Bernard J.; Cheng, Gary J.; Moffett, David F.; Kidwell, David A.

    2008-01-01

    This paper presents a novel method for making micron-sized apertures with tapered sidewalls and nano-sized apertures. Their use in bilayer lipid membrane-based ion selective electrode design is demonstrated and compared to mesoscale bilayers and traditional PVC ion selective electrodes. Micron-sized apertures are fabricated in SU-8 photoresist films and vary in diameter from 10 to 40 microns. The tapered edges in SU-8 films are desired to enhance bilayer lipid membrane (BLM) formation and are...

  9. Transport-limited water splitting at ion-selective interfaces during concentration polarization

    DEFF Research Database (Denmark)

    Nielsen, Christoffer Peder; Bruus, Henrik

    2014-01-01

    We present an analytical model of salt- and water-ion transport across an ion-selective interface based on an assumption of local equilibrium of the water-dissociation reaction. The model yields current-voltage characteristics and curves of water-ion current versus salt-ion current, which....... These solutions provide closed-form expressions for the current-voltage characteristics, which include the overlimiting current due to the development of an extended space-charge region. Finally, we discuss how the addition of an acid or a base affects the transport properties of the system and thus provide...

  10. In Situ SIMS and IR Spectroscopy of Well-Defined Surfaces Prepared by Soft Landing of Mass-Selected Ions

    Energy Technology Data Exchange (ETDEWEB)

    Johnson, Grant E.; Gunaratne, Kalupathirannehelage Don D.; Laskin, Julia

    2014-06-16

    Soft landing of mass-selected ions onto surfaces is a powerful approach for the highly-controlled preparation of materials that are inaccessible using conventional synthesis techniques. Coupling soft landing with in situ characterization using secondary ion mass spectrometry (SIMS) and infrared reflection absorption spectroscopy (IRRAS) enables analysis of well-defined surfaces under clean vacuum conditions. The capabilities of three soft-landing instruments constructed in our laboratory are illustrated for the representative system of surface-bound organometallics prepared by soft landing of mass-selected ruthenium tris(bipyridine) dications, [Ru(bpy)3]2+, onto carboxylic acid terminated self-assembled monolayer surfaces on gold (COOH-SAMs). In situ time-of-flight (TOF)-SIMS provides insight into the reactivity of the soft-landed ions. In addition, the kinetics of charge reduction, neutralization and desorption occurring on the COOH-SAM both during and after ion soft landing are studied using in situ Fourier transform ion cyclotron resonance (FT-ICR)-SIMS measurements. In situ IRRAS experiments provide insight into how the structure of organic ligands surrounding metal centers is perturbed through immobilization of organometallic ions on COOH-SAM surfaces by soft landing. Collectively, the three instruments provide complementary information about the chemical composition, reactivity and structure of well-defined species supported on surfaces.

  11. Synthesis of tripodal trifluoroacetophenone derivatives and their evaluation as ion-selective electrode membranes

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Young Kook; Ahn, Kyo Han [POSTECH, Pohang (Korea, Republic of); Ha, Jeong Han; Cha, Geun Sig [Kwangwoon Univ., Seoul (Korea, Republic of)

    2002-10-01

    New, C{sub 3} symmetric, tripodal trifluoroacetophenone derivatives 1-3 have been synthesized as anion ionophores. Evaluation of their ion selectivity has been carried out through ion-selective electrode membranes. The selectivity coefficients for the carbonates electrode toward various anions are dependent on the composition of the membranes and the lipophilicity of the ionophores. The tripodal ionophore 1a showed an improved selectivity toward salicylate when 90 mol% of a lipophilic additive was used, compared to that of p-dodecyltrifluoroacetophenone.

  12. The facet selectivity of inorganic ions on silver nanocrystals in etching reactions

    Energy Technology Data Exchange (ETDEWEB)

    Xu Shuping; Tang Bin; Zheng Xianliang; Zhou Ji; An Jing; Ning Xiaohua; Xu Weiqing, E-mail: xuwq@jlu.edu.cn [State Key Laboratory of Supramolecular Structure and Materials, Jilin University, Changchun 130012 (China)

    2009-10-14

    The facet selectivity of the halide ions and chlorauric acid for several shaped silver nanocrystals is presented in this paper. Two inorganic ions show different representations when they are used for etching silver nanocrystals in the self-sacrificial template reaction. The morphological changes of the silver nanocrystals indicate that the halide ions prefer to etch the (110) facets of silver nanocrystals, while in the chlorauric acid etching reaction, gold first modifies the (110) facets and then lets chlorauric acid etch the (111) facets instead. The selective facet etching on individual nanoparticles in the solution phase has crucial significance in the control-synthesis of nanocrystals and the facet asymmetric reaction.

  13. High mass-resolution electron-ion-ion coincidence measurements on core-excited organic molecules

    CERN Document Server

    Tokushima, T; Senba, Y; Yoshida, H; Hiraya, A

    2001-01-01

    Total electron-ion-ion coincidence measurements on core excited organic molecules have been carried out with high mass resolution by using multimode (reflectron/linear) time-of-flight mass analyzer. From the ion correlation spectra of core excited CH sub 3 OH and CD sub 3 OH, the reaction pathway to form H sub 3 sup + (D sub 3 sup +) is identified as the elimination of three H (D) atoms from the methyl group, not as the inter-group (-CH sub 3 and -OH) interactions. In a PEPIPICO spectrum of acetylacetone (CH sub 3 COCH sub 2 COCH sub 3) measured by using a reflectron TOF, correlations between ions up to mass number 70 with one-mass resolution was recorded.

  14. Dopant Selective Reactive Ion Etching of Silicon Carbide

    Science.gov (United States)

    Okojie, Robert (Inventor)

    2016-01-01

    A method for selectively etching a substrate is provided. In one embodiment, an epilayer is grown on top of the substrate. A resistive element may be defined and etched into the epilayer. On the other side of the substrate, the substrate is selectively etched up to the resistive element, leaving a suspended resistive element.

  15. Formation of high intensity ion beams with ballistic focusing

    Science.gov (United States)

    Koval, T. V.; Ryabchikov, A. I.; Shevelev, A. E.; Kim, An Tran My; Tarakanov, V. P.

    2017-11-01

    This investigation presents the results of experimental investigation and theoretical simulations of the influence of plasma and negative bias parameters on formation, transportation and focusing of high intensity ion beams of titanium and nitrogen (with an ion current density up to 1 A/cm2 and pulsed power density up to 2.6 kW/cm2). It was shown that the conditions of space charge neutralization of the focusing beam have a significant influence on the distribution and magnitude of the ion current at the collector.

  16. Advanced approaches to high intensity laser-driven ion acceleration

    Energy Technology Data Exchange (ETDEWEB)

    Henig, Andreas

    2010-04-26

    Since the pioneering work that was carried out 10 years ago, the generation of highly energetic ion beams from laser-plasma interactions has been investigated in much detail in the regime of target normal sheath acceleration (TNSA). Creation of ion beams with small longitudinal and transverse emittance and energies extending up to tens of MeV fueled visions of compact, laser-driven ion sources for applications such as ion beam therapy of tumors or fast ignition inertial con finement fusion. However, new pathways are of crucial importance to push the current limits of laser-generated ion beams further towards parameters necessary for those applications. The presented PhD work was intended to develop and explore advanced approaches to high intensity laser-driven ion acceleration that reach beyond TNSA. In this spirit, ion acceleration from two novel target systems was investigated, namely mass-limited microspheres and nm-thin, free-standing diamond-like carbon (DLC) foils. Using such ultrathin foils, a new regime of ion acceleration was found where the laser transfers energy to all electrons located within the focal volume. While for TNSA the accelerating electric field is stationary and ion acceleration is spatially separated from laser absorption into electrons, now a localized longitudinal field enhancement is present that co-propagates with the ions as the accompanying laser pulse pushes the electrons forward. Unprecedented maximum ion energies were obtained, reaching beyond 0.5 GeV for carbon C{sup 6+} and thus exceeding previous TNSA results by about one order of magnitude. When changing the laser polarization to circular, electron heating and expansion were shown to be efficiently suppressed, resulting for the first time in a phase-stable acceleration that is dominated by the laser radiation pressure which led to the observation of a peaked C{sup 6+} spectrum. Compared to quasi-monoenergetic ion beam generation within the TNSA regime, a more than 40 times

  17. Improved ion-selective detection method using nanopipette with poly(vinyl chloride)-based membrane.

    Science.gov (United States)

    Kang, Eun Ji; Takami, Tomohide; Deng, Xiao Long; Son, Jong Wan; Kawai, Tomoji; Park, Bae Ho

    2014-05-15

    Ion-selective electrodes (ISEs) are widely used to detect targeted ions in solution selectively. Application of an ISE to a small area detection system with a nanopipette requires a special measurement method in order to avoid the enhanced background signal problem caused by a cation-rich layer near the charged inner surface of the nanopipette and the selectivity change problem due to relatively fast saturation of the ISE inside the nanopipette. We developed a novel ion-selective detection system using a nanopipette that measures an alternating current (AC) signal mediated by saturated ionophores in a poly(vinyl chloride) (PVC) membrane located at the conical shank of the nanopipette to solve the above problems. Small but reliable K(+) and Na(+) ionic current passing through a PVC membrane containing saturated bis(benzo-15-crown-5) and bis(12-crown-4) ionophore, respectively, could be selectively detected using the AC signal measurement system equipped with a lock-in amplifier.

  18. Strong-field relativistic processes in highly charged ions

    Energy Technology Data Exchange (ETDEWEB)

    Postavaru, Octavian

    2010-12-08

    In this thesis we investigate strong-field relativistic processes in highly charged ions. In the first part, we study resonance fluorescence of laser-driven highly charged ions in the relativistic regime by solving the time-dependent master equation in a multi-level model. Our ab initio approach based on the Dirac equation allows for investigating highly relativistic ions, and, consequently, provides a sensitive means to test correlated relativistic dynamics, bound-state quantum electrodynamic phenomena and nuclear effects by applying coherent light with x-ray frequencies. Atomic dipole or multipole moments may be determined to unprecedented accuracy by measuring the interference-narrowed fluorescence spectrum. Furthermore, we investigate the level structure of heavy hydrogenlike ions in laser beams. Interaction with the light field leads to dynamic shifts of the electronic energy levels, which is relevant for spectroscopic experiments. We apply a fully relativistic description of the electronic states by means of the Dirac equation. Our formalism goes beyond the dipole approximation and takes into account non-dipole effects of retardation and interaction with the magnetic field components of the laser beam. We predicted cross sections for the inter-shell trielectronic recombination (TR) and quadruelectronic recombination processes which have been experimentally confirmed in electron beam ion trap measurements, mainly for C-like ions, of Ar, Fe and Kr. For Kr{sup 30}+, inter-shell TR contributions of nearly 6% to the total resonant photorecombination rate were found. (orig.)

  19. Ion Based High-Temperature Pressure Sensor

    National Research Council Canada - National Science Library

    Zdenek, Jeffrey S; Anthenien, Ralph A

    2004-01-01

    .... The environment encountered in such engines necessitates high temperature and durable (vibration resistant) devices. Traditional pressure sensors can be used, however thermal insulating materials must be used to protect the diaphragm...

  20. LITERATURE REVIEWS TO SUPPORT ION EXCHANGE TECHNOLOGY SELECTION FOR MODULAR SALT PROCESSING

    Energy Technology Data Exchange (ETDEWEB)

    King, W

    2007-11-30

    This report summarizes the results of literature reviews conducted to support the selection of a cesium removal technology for application in a small column ion exchange (SCIX) unit supported within a high level waste tank. SCIX is being considered as a technology for the treatment of radioactive salt solutions in order to accelerate closure of waste tanks at the Savannah River Site (SRS) as part of the Modular Salt Processing (MSP) technology development program. Two ion exchange materials, spherical Resorcinol-Formaldehyde (RF) and engineered Crystalline Silicotitanate (CST), are being considered for use within the SCIX unit. Both ion exchange materials have been studied extensively and are known to have high affinities for cesium ions in caustic tank waste supernates. RF is an elutable organic resin and CST is a non-elutable inorganic material. Waste treatment processes developed for the two technologies will differ with regard to solutions processed, secondary waste streams generated, optimum column size, and waste throughput. Pertinent references, anticipated processing sequences for utilization in waste treatment, gaps in the available data, and technical comparisons will be provided for the two ion exchange materials to assist in technology selection for SCIX. The engineered, granular form of CST (UOP IE-911) was the baseline ion exchange material used for the initial development and design of the SRS SCIX process (McCabe, 2005). To date, in-tank SCIX has not been implemented for treatment of radioactive waste solutions at SRS. Since initial development and consideration of SCIX for SRS waste treatment an alternative technology has been developed as part of the River Protection Project Waste Treatment Plant (RPP-WTP) Research and Technology program (Thorson, 2006). Spherical RF resin is the baseline media for cesium removal in the RPP-WTP, which was designed for the treatment of radioactive waste supernates and is currently under construction in Hanford, WA

  1. 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.

  2. Fluorescent iminodiacetamide derivatives as potential ionophores for optical zinc ion-selective sensors.

    Science.gov (United States)

    Urbanová, Nikoleta; Kádár, Mihály; Tóth, Klára; Bogáti, Botond; Andruch, Vasil; Bitter, István

    2008-06-01

    Fluorescent sensor molecules were synthesized by conjugation of iminodiacetamide derivatives with fluorescent moieties of different structures and their UV-visible and fluorescent properties were characterized in acetonitrile solvent. The fluorescent measurements revealed that the N-(2-naphthyl) and N-phenyl derivatives exhibit a distinct zinc ion-selectivity over alkali and alkaline earth metal ions, while N-(anthrylmethyl) and N-(3-methoxyphenyl) derivatives do not possess any ion-selectivities. In contrast to the fluorescent measurements, all ligands show Zn(2+) selectivity over Ca(2+) and Mg(2+) ions in plasticized PVC membranes using potentiometric signal transduction. This observation found for N-(anthrylmethyl) and N-(3-methoxyphenyl) derivatives can be ascribed to the more hindered interaction between the signalling group of the ionophore and the central metal ion in PVC membranes than in acetonitrile solution upon complexation. From the fluorescent measurements it can also be concluded that the ligands with metal ions form complexes mainly with 2:1 stoichiometry (L(2)M). On complex formation a considerable decrease in the fluorescent intensity was observed for all ligands except the N-(anthrylmethyl) derivative, where a 25 - 30 fold fluorescence enhancement was found, which is explained by the photoinduced electron transfer (PET) mechanism. All ionophores exhibited serious hydrogen ion interference, therefore complexation-induced spectral changes were measured in aprotic acetonitrile solution.

  3. Photorecombination studies of highly charged tungsten ions at Shanghai EBIT

    Science.gov (United States)

    Tu, B.; Xiao, J.; Yao, K.; Wang, X.; Shen, Y.; Yang, Y.; Lu, D.; Huang, L.; Zhen, C.; Fu, Y.; Wei, B.; Hutton, R.; Zou, Y.

    2017-11-01

    In this paper, we report studies on photorecombination (PR) processes for highly charged W ions. The experiment was performed at Shanghai electron beam ion trap by employing a fast electron beam-energy scanning technique. The KLL dielectronic recombination (DR) resonance strengths for He- up to O-like W ions were determined. The strong interference effect between DR and radiative recombination (RR) was observed and the Fano factor, which measures the interference degree, was determined for the main resonances of ground state He-, Be-, B-, C-, N-, and O-like W ions. In addition, we show experimentally that an autoionizing state can have both Fano and Lorentzian behavior naturally, depending on the processes involved. A fully relativistic configuration interaction method implemented in the flexible atomic code was employed to calculate DR, RR processes and also the inference effect.

  4. High intensity ion beams in rf undulator linac

    Directory of Open Access Journals (Sweden)

    E. S. Masunov

    2008-07-01

    Full Text Available The possibility of using a radio frequency undulator field to accelerate a high intensity ion beam in a linac is discussed. Such an accelerator can be realized using the periodical interdigital H-type resonator structure. The accelerating force is produced by an electric field which is a combination of two or more spatial harmonics, none of them being synchronous with the ion beam. The value of this force is proportional to the squared charge. The equations of motion in Hamiltonian form are derived by means of smooth approximation. The analysis of the 3D effective potential function allows finding the conditions of the beam focusing and acceleration. Two ways to increase ion beam intensity are considered: (i to enlarge beam cross section; (ii to neutralize the beam space charge by accelerating ions with opposite charge signs within the same bunch. The basic results are confirmed by a numerical simulation.

  5. Review of progresses on clinical applications of ion selective electrodes for electrolytic ion tests: from conventional ISEs to graphene-based ISEs

    Directory of Open Access Journals (Sweden)

    Rongguo Yan

    2016-10-01

    Full Text Available There exist several positively and negatively charged electrolytes or ions in human blood, urine, and other body fluids. Tests that measure the concentration of these ions in clinics are performed using a more affordable, portable, and disposable potentiometric sensing method with few sample volumes, which requires the use of ion-selective electrodes (ISEs and reference electrodes. This review summarily descriptively presents progressive developments and applications of ion selective electrodes in medical laboratory electrolytic ion tests, from conventional ISEs, solid-contact ISEs, carbon nanotube based ISEs, to graphene-based ISEs.

  6. Development of a disposable mercury ion-selective optode based on tritylpicolinamide as ionophore

    NARCIS (Netherlands)

    Kuswandi, Bambang; Nuriman, [Unknown; Dam, H.H.; Reinhoudt, David; Verboom, Willem

    2007-01-01

    A disposable ion-selective optode for mercury based on trityl-picolinamide (T-Pico) as neutral ionophore was developed. The sensing layer consist of plasticised PVC incorporating T-Pico as a selective ionophore for Hg2+, ETH 5418 as a chromoionophore, and potassium

  7. Studies of copper(II) sulphide ion-selective electrodes.

    Science.gov (United States)

    Johansson, G; Edström, K

    1972-12-01

    Changes in liquid junction potentials in copper(II) solutions were measured when different reference electrodes were used. The slope and intercept of a calibration curve for a copper-selective electrode will depend on the selection of reference electrode. The condition of the electrode surface of an Orion copper-selective electrode was studied microscopically and the influence of redox potential on stability of the electrode against corrosion is discussed. Oxidizing solutions will produce pits at dislocations in the material and there will be a mixed electrode potential. The slope, stability, and speed of response are much lower when the surface contains pits. Diamond-polishing was shown to improve the electrode significantly.

  8. How simple is too simple? Computational perspective on importance of second-shell environment for metal-ion selectivity.

    Science.gov (United States)

    Gutten, Ondrej; Rulíšek, Lubomír

    2015-06-14

    The metal-ion selectivity in biomolecules represents one of the most important phenomena in bioinorganic chemistry. The open question to what extent is the selectivity in the complex bioinorganic structures such as metallopeptides determined by the first-shell ligands of the metal ion is answered herein using six model peptides complexed with the set of divalent metal ions (Mn(2+), Fe(2+), Co(2+), Ni(2+), Cu(2+), Zn(2+), Cd(2+), and Hg(2+)) and their various first-shell representations. By calculating the differences among the free energies of complexation of metal ions in these peptides and their model (truncated) systems it is quantitatively shown that the definition of the first shell is paramount to this discussion and revolves around the chemical nature of the binding site. Despite the vast conceivable diversity of peptidic structures, that suggest certain fluidity of this definition, major contributing factors are identified and assessed based on their importance for capturing metal-ion selectivity. These factors include soft/hard character of ligands and various non-covalent interactions in the vicinity of the binding site. The relative importance of these factors is considered and specific suggestions for effective construction of the models are made. The relationship of first-shell models and their corresponding parent peptides is discussed thoroughly, both with respect to their chemical similarity and potential disparity introduced by generally "non-alignable" conformational flexibility of the two systems. It is concluded that, in special cases, this disparity can be negligible and that heeding the chemical factors contributing to selectivity during construction of the model can successfully result in models that retain the affinity profile for various metal ions with high fidelity.

  9. Selective injection and isolation of ions in quadrupole ion trap mass spectrometry using notched waveforms created using the inverse Fourier transform

    Energy Technology Data Exchange (ETDEWEB)

    Soni, M.H.; Cooks, R.G. (Purdue Univ., West Lafayette, IN (United States))

    1994-08-01

    Broad-band excitation of ions is accomplished in the quadrupole ion trap mass spectrometer using notched waveforms created by the SWIFT (stored waveform inverse Fourier transform) technique. A series of notched SWIFT pulses are applied during the period of ion injection from an external Cs[sup +] source to resonantly eject all ions whose resonance frequencies fall within the frequency range of the pulse while injecting only those analyte ions whose resonance frequencies fall within the limits of the notch. This allows selective injection and accumulation of the ions of interest and continuous ejection of the unwanted ions. This is shown to result in significant improvement in S/N ratio, resolution, and sensitivity for the analyte ions of interest. Selective ion injection is demonstrated by injecting the protonated molecules of peptides VSV and gramicidin S and the intact cation of l-carnitine hydrochloride, using singly notched SWIFT pulses. Multiply notched SWIFT pulses are used to simultaneously inject ions of different m/z values of l-carnitine hydrochloride into the ion trap. A new coarse/fine ion isolation procedure, which employs a doubly notched SWIFT pulse, is demonstrated for isolating ions of a single m/z value of 4-bromobiphenyl from a population of trapped ions. 36 refs., 10 figs., 2 tabs.

  10. Evaluation of selected ion exchangers for the removal of cesium from MVST W-25 supernate

    Energy Technology Data Exchange (ETDEWEB)

    Collins, J.L.; Egan, B.Z.; Anderson, K.K.; Chase, C.W.; Mrochek, J.E.; Bell, J.T.; Jernigan, G.E.

    1995-04-01

    The goal of this batch-test equilibration study was to evaluate the effectiveness of certain ion exchangers for removing cesium from supernate taken from tank W-25 of the Melton Valley Storage Tank (MVST) Facility located at the Oak Ridge National Laboratory (ORNL). These exchangers were selective for removing cesium from alkaline supernatant solutions with high salt concentrations. Since the supernates of evaporator concentrates stored in tanks at the MVST facility have compositions similar to some of those stored in tanks at Hanford, the data generated in this study should prove useful in the overall evaluation of the ion exchangers for applications to Hanford and other US Department of Energy (USDOE) sites. A goal of the waste processing effort at Hanford is to remove enough cesium to ensure that the resulting LLW will meet the Nuclear Regulatory Commission (NRC) 10 CFR 61 class A limit for {sup 137}Cs (1 Ci/m{sup 3} or 1 {mu}Ci/mL). The separated cesium may be concentrated and vitrified for disposal in the high-level waste repository. The decontaminated effluent would be solidified for near-surface disposal.

  11. [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.

  12. Cold highly charged ions in a cryogenic Paul trap

    DEFF Research Database (Denmark)

    Versolato, O.O.; Schwarz, M.; Windberger, A.

    2013-01-01

    Narrow optical transitions in highly charged ions (HCIs) are of particular interest for metrology and fundamental physics, exploiting the high sensitivity of HCIs to new physics. The highest sensitivity for a changing fine structure constant ever predicted for a stable atomic system is found in Ir...

  13. 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.

  14. Relativistic, QED and nuclear effects in highly charged ions revealed by resonant electron-ion recombination in storage rings

    OpenAIRE

    Schippers, Stefan

    2008-01-01

    Dielectronic recombination (DR) of few-electron ions has evolved into a sensitive spectroscopic tool for highly charged ions. This is due to technological advances in electron-beam preparation and ion-beam cooling techniques at heavy-ion storage rings. Recent experiments prove unambiguously that DR collision spectroscopy has become sensitive to 2nd order QED and to nuclear effects. This review discusses the most recent developments in high-resolution spectroscopy of low-energy DR resonances, ...

  15. Fabrication, calibration and evaluation of a phosphate ion-selective microelectrode

    Energy Technology Data Exchange (ETDEWEB)

    Wang, John J., E-mail: johnwang1974@gmail.co [University of Cincinnati, 12716 Ginger Wood Lane, Clarksburg, MD 20871 (United States); Bishop, Paul L. [Department of Civil and Environmental Engineering, PO Box 210071, University of Cincinnati, Cincinnati, OH 45221-0071 (United States)

    2010-12-15

    To conduct the micro-environment study of flocs in an enhanced biological phosphorus removal (EBPR) process, a phosphate ion-selective microelectrode was developed. The cobalt-based microelectrodes have tip diameters of 5-20 {mu}m and respond to all the three forms of phosphate ions, namely, H{sub 2}PO{sub 4}{sup -}, HPO{sub 4}{sup 2-}, and PO{sub 4}{sup 3-}. The calibration curve at pH 7.5 had a slope of 31.5 mV per decade change of concentration and a R{sup 2} value of 0.99. Other characteristics of this microelectrode, such as response time, interferences from pH, ion strength, DO and other anions were also evaluated. - This paper presents the first phosphate ion-selective microelectrode in the world used for micro-level phorphorus removal studies.

  16. Ion aggregation in high salt solutions. V. Graph entropy analyses of ion aggregate structure and water hydrogen bonding network

    Science.gov (United States)

    Choi, Jun-Ho; Cho, Minhaeng

    2016-05-01

    Dissolved ions in water tend to form polydisperse ion aggregates such as ion pairs, relatively compact ion clusters, and even spatially extended ion networks with increasing salt concentration. Combining molecular dynamics simulation and graph theoretical analysis methods, we recently studied morphological structures of ion aggregates with distinctively different characteristics. They can be distinguished from each other by calculating various spectral graph theoretical properties such as eigenvalues and eigenvectors of adjacency matrices of ion aggregates and water hydrogen-bonding networks, minimum path lengths, clustering coefficients, and degree distributions. Here, we focus on percolation and graph entropic properties of ion aggregates and water hydrogen-bonding networks in high salt solutions. Ion network-forming K+ and SCN- ions at high concentrations show a percolating behavior in their aqueous solutions, but ion cluster-forming ions in NaCl solutions do not show such a transition from isolated ion aggregates to percolating ion-water mixture morphology. Despite that the ion aggregate structures are strikingly different for either cluster- or network-forming ions in high salt solutions, it is interesting that the water structures remain insensitive to the electrostatic properties, such as charge densities and polydentate properties, of dissolved ions, and morphological structures of water H-bonding networks appear to be highly robust regardless of the nature and concentration of salt. We anticipate that the present graph entropy analysis results would be of use in understanding a variety of anomalous behaviors of interfacial water around biomolecules as well as electric conductivities of high electrolyte solutions.

  17. Ion aggregation in high salt solutions. V. Graph entropy analyses of ion aggregate structure and water hydrogen bonding network.

    Science.gov (United States)

    Choi, Jun-Ho; Cho, Minhaeng

    2016-05-28

    Dissolved ions in water tend to form polydisperse ion aggregates such as ion pairs, relatively compact ion clusters, and even spatially extended ion networks with increasing salt concentration. Combining molecular dynamics simulation and graph theoretical analysis methods, we recently studied morphological structures of ion aggregates with distinctively different characteristics. They can be distinguished from each other by calculating various spectral graph theoretical properties such as eigenvalues and eigenvectors of adjacency matrices of ion aggregates and water hydrogen-bonding networks, minimum path lengths, clustering coefficients, and degree distributions. Here, we focus on percolation and graph entropic properties of ion aggregates and water hydrogen-bonding networks in high salt solutions. Ion network-forming K(+) and SCN(-) ions at high concentrations show a percolating behavior in their aqueous solutions, but ion cluster-forming ions in NaCl solutions do not show such a transition from isolated ion aggregates to percolating ion-water mixture morphology. Despite that the ion aggregate structures are strikingly different for either cluster- or network-forming ions in high salt solutions, it is interesting that the water structures remain insensitive to the electrostatic properties, such as charge densities and polydentate properties, of dissolved ions, and morphological structures of water H-bonding networks appear to be highly robust regardless of the nature and concentration of salt. We anticipate that the present graph entropy analysis results would be of use in understanding a variety of anomalous behaviors of interfacial water around biomolecules as well as electric conductivities of high electrolyte solutions.

  18. Development of a fully integrated analysis system for ions based on ion-selective optodes and centrifugal microfluidics

    Science.gov (United States)

    Johnson, R. D.; Badr, I. H.; Barrett, G.; Lai, S.; Lu, Y.; Madou, M. J.; Bachas, L. G.; Daunert, S. (Principal Investigator)

    2001-01-01

    A fully integrated, miniaturized analysis system for ions based on a centrifugal microfluidics platform and ion-selective optode membranes is described. The microfluidic architecture is composed of channels, five solution reservoirs, a measuring chamber, and a waste reservoir manufactured onto a disk-shaped substrate of poly(methyl methacrylate). Ion-selective optode membranes, composed of plasticized poly(vinyl chloride) impregnated with an ionophore, a proton chromoionophore, and a lipophilic anionic additive, were cast, with a spin-on device, onto a support layer and then immobilized on the disk. Fluid propulsion is achieved by the centrifugal force that results from spinning the disk, while a system of valves is built onto the disk to control flow. These valves operate based on fluid properties and fluid/substrate interactions and are controlled by the angular frequency of rotation. With this system, we have been able to deliver calibrant solutions, washing buffers, or "test" solutions to the measuring chamber where the optode membrane is located. An analysis system based on a potassium-selective optode has been characterized. Results indicate that optodes immobilized on the platform demonstrate theoretical responses in an absorbance mode of measurement. Samples of unknown concentration can be quantified to within 3% error by fitting the response function for a given optode membrane using an acid (for measuring the signal for a fully protonated chromoionophore), a base (for fully deprotonated chromoionophore), and two standard solutions. Further, the ability to measure ion concentrations by employing one standard solution in conjunction with acid and base and with two standards alone were studied to delineate whether the current architecture could be simplified. Finally, the efficacy of incorporating washing steps into the calibration protocol was investigated.

  19. Improved design for high resolution electrospray ionization ion mobility spectrometry.

    Science.gov (United States)

    Jafari, M T

    2009-03-15

    An improved design for high resolution electrospray ionization ion mobility spectrometry (ESI-IMS) was developed by making some salient modifications to the IMS cell and its performance was investigated. To enhance desolvation of electrospray droplets at high sample flow rates in this new design, volume of the desolvation region was decreased by reducing its diameter and the entrance position of the desolvation gas was shifted to the end of the desolvation region (near the ion gate). In addition, the ESI source (both needle and counter electrode) was positioned outside of the heating oven of the IMS. This modification made it possible to use the instrument at higher temperatures, and preventing needle clogging in the electrospray process. The ion mobility spectra of different chemical compounds were obtained. The resolving power and resolution of the instrument were increased by about 15-30% relative to previous design. In this work, the baseline separation of the two adjacent ion peaks of morphine and those of codeine was achieved for the first time with resolutions of 1.5 and 1.3, respectively. These four ion peaks were well separated from each other using carbon dioxide (CO(2)) rather than nitrogen as the drift gas. Finally, the analytical parameters obtained for ethion, metalaxyl, and tributylamine indicated the high performance of the instrument for quantitative analysis.

  20. Effects of High Pressure on Membrane Ion Binding and Transport.

    Science.gov (United States)

    1980-12-31

    AD-AI16 015 CALIFORNIA UNIV BERKELEY DEPT OF PHYSIOLOGY- ANATOMY FIG 6/16 EFFECTS OF HIGH PRESSURE ON MEMBRANE ION BINDING AND TRANSPORT.(U) DEC 80 R...ION BIND.NG AID TPANSPOFT (N)014-7 1-C-0482) 1Fobert I. 1.. cey, Ph.D. a v] Da iel M. F zan, Ph.D. Department of Ph ,sioloy- Anatomy unriveorsity o...given to Tra"uble’s theory . C. Develonrment of a High Pressure Zton-Flow Realization of the goals outlined in this project lenends on the availa- bility

  1. Production technology for high efficiency ion implanted solar cells

    Science.gov (United States)

    Kirkpatrick, A. R.; Minnucci, J. A.; Greenwald, A. C.; Josephs, R. H.

    1978-01-01

    Ion implantation is being developed for high volume automated production of silicon solar cells. An implanter designed for solar cell processing and able to properly implant up to 300 4-inch wafers per hour is now operational. A machine to implant 180 sq m/hr of solar cell material has been designed. Implanted silicon solar cells with efficiencies exceeding 16% AM1 are now being produced and higher efficiencies are expected. Ion implantation and transient processing by pulsed electron beams are being integrated with electrostatic bonding to accomplish a simple method for large scale, low cost production of high efficiency solar cell arrays.

  2. Studies on Calcium Ion Selectivity of ZnO Nanowire Sensors Using Ionophore Membrane Coatings

    Directory of Open Access Journals (Sweden)

    M. H. Asif

    2008-01-01

    Full Text Available Zinc oxide nanorods with 100 nm diameter and 900 nm length were grown on the surface of a silver wire (0.25 mm in diameter with the aim to produce electrochemical nanosensors. It is shown that the ZnO nanorods exhibit a Ca2+-dependent electrochemical potentiometric behavior in an aqueous solution. The potential difference was found to be linear over a large logarithmic concentration range (1 M to 0.1 M using Ag/AgCl as a reference electrode and the response time was less than one minute. In order to adapt the sensors for calcium ion measurements in biological fluids with sufficient selectivity and stability, plastic membrane coatings containing ionophores were applied. These functionalized ZnO nanorods sensors showed a high sensitivity (26.55 mV/decade and good stability.

  3. State selective electron capture studies with slow state prepared ion beams

    CERN Document Server

    McCullough, R W

    1999-01-01

    Double translational energy spectroscopy has been successfully used to study state selective electron capture processes in atomic and molecular targets involving slow ( nu <1 au) C/sup 2+/, N/sup 2+/ and O/sup 2+/ primary ions in prepared ground or metastable states. The results show that previous TES and total one electron capture measurements involving primary ions beams containing unknown fractions of metastable states require cautious interpretation. (22 refs).

  4. Potentiometric determination of K+ ions using a K+-selective electrode with macrocyclic liquid membrane

    Directory of Open Access Journals (Sweden)

    Cezar Spinu

    2008-08-01

    Full Text Available This paper describes analytical applications of K+-selective liquid membrane electrode. Themembrane is the solution of the active complex formed by the K+ ions with dibenzo-18-crown-6 ionophore (DB-[18]-C-6 extracted in propylenecarbonate (PC. Successful application of the developed electrode for K+ ions determination in aqueous solution and samples of commercial mineral water by direct potentiometry is presented.

  5. Functional polythiophene nanoparticles: Size-controlled electropolymerization and ion selective response

    DEFF Research Database (Denmark)

    Si, P.C.; Chi, Qijin; Li, Z.S.

    2007-01-01

    We have synthesized a thiophene derivative, (4-benzeno-15-crown-5 ether)-thiophene-3-methylene-amine (BTA), which was used as a monomer for electrochemical polymerization on metallic surfaces to prepare functional polymer films. Self-assembly of BTA monomers on Au(111) surfaces promotes ordered...... solution and organic phase on gold electrodes, displayed selective sensitivity to potassium ions with a linear dependence of ion concentration over 4 orders of magnitude....

  6. Measurement of charge exchange cross sections for highly charged xenon and thorium ions with molecular hydrogen in a Penning Ion Trap

    Energy Technology Data Exchange (ETDEWEB)

    Weinberg, G.M.

    1995-12-01

    Highly charged xenon (35+ to 46+) and thorium (72+ to 79+) ions were produced in an Electron Beam Ion Trap (EBIT). The ions were extracted from EBIT in a short pulse. Ions of one charge state were selected using an electromagnet. The ions were recaptured at low energy in a cryogenic Penning trap (RETRAP). As the ions captured electrons from molecular hydrogen, populations of the various charge states were obtained by measuring the image currents induced by the ions on the electrodes of the trap. Data on the number of ions in each charge state vs. time were compared to theoretical rate equations in order to determine the average charge exchange rates. These rates were compared to charge exchange rates of an ion with a known charge exchange cross section (Ar{sup 11+}) measured in a similar manner in order to determine the average charge exchange cross sections for the highly charged ions. The energy of interaction between the highly charged ions and hydrogen was estimated to be 4 eV in the center of mass frame. The mean charge exchange cross sections were 9 {times} 10{sup {minus}14} cm{sup 2} for Xe{sup 43+} to Xe{sup 46+} and 2 {times} 10{sup {minus}13} cm{sup 2} for Th{sup 73+} to Th{sup 79+}. Double capture was approximately 20--25% of the total for both xenon and thorium. A fit indicated that the cross sections were approximately proportional to q. This is consistent with a linear dependence of cross section on q within the measurement uncertainties.

  7. DIAGNOSTICS FOR ION BEAM DRIVEN HIGH ENERGY DENSITY PHYSICS EXPERIMENTS

    Energy Technology Data Exchange (ETDEWEB)

    Bieniosek, F.M.; Henestroza, E.; Lidia, S.; Ni, P.A.

    2010-01-04

    Intense beams of heavy ions are capable of heating volumetric samples of matter to high energy density. Experiments are performed on the resulting warm dense matter (WDM) at the NDCX-I ion beam accelerator. The 0.3 MeV, 30-mA K{sup +} beam from NDCX-I heats foil targets by combined longitudinal and transverse neutralized drift compression of the ion beam. Both the compressed and uncompressed parts of the NDCX-I beam heat targets. The exotic state of matter (WDM) in these experiments requires specialized diagnostic techniques. We have developed a target chamber and fielded target diagnostics including a fast multi-channel optical pyrometer, optical streak camera, laser Doppler-shift interferometer (VISAR), beam transmission diagnostics, and high-speed gated cameras. We also present plans and opportunities for diagnostic development and a new target chamber for NDCX-II.

  8. A Change in the Ion Selectivity of Ligand-Gated Ion Channels Provides a Mechanism to Switch Behavior.

    Directory of Open Access Journals (Sweden)

    Jennifer K Pirri

    Full Text Available Behavioral output of neural networks depends on a delicate balance between excitatory and inhibitory synaptic connections. However, it is not known whether network formation and stability is constrained by the sign of synaptic connections between neurons within the network. Here we show that switching the sign of a synapse within a neural circuit can reverse the behavioral output. The inhibitory tyramine-gated chloride channel, LGC-55, induces head relaxation and inhibits forward locomotion during the Caenorhabditis elegans escape response. We switched the ion selectivity of an inhibitory LGC-55 anion channel to an excitatory LGC-55 cation channel. The engineered cation channel is properly trafficked in the native neural circuit and results in behavioral responses that are opposite to those produced by activation of the LGC-55 anion channel. Our findings indicate that switches in ion selectivity of ligand-gated ion channels (LGICs do not affect network connectivity or stability and may provide an evolutionary and a synthetic mechanism to change behavior.

  9. Isotope and ion selectivity in reverse osmosis desalination: geochemical tracers for man-made freshwater.

    Science.gov (United States)

    Kloppmann, Wolfram; Vengosh, Avner; Guerrot, Catherine; Millot, Romain; Pankratov, Irena

    2008-07-01

    A systematic measurement of ions and 2H/1H, 7Li/6Li, 11B/10B, 18O/ 16O, and 87Sr/86Sr isotopes in feed-waters, permeates, and brines from commercial reverse osmosis (RO) desalination plants in Israel (Ashkelon, Eilat, and Nitzana) and Cyprus (Larnaca) reveals distinctive geochemical and isotopic fingerprints of fresh water generated from desalination of seawater (SWRO) and brackish water (BWRO). The degree of isotope fractionation during the passage of water and solutes through the RO membranes depends on the medium (solvent-water vs. solutes), chemical speciation of the solutes, their charge, and their mass difference. O, H, and Sr isotopes are not fractionated during the RO process. 7Li is preferentially rejected in low pH RO, and B isotope fractionation depends on the pH conditions. Under low pH conditions, B isotopes are not significantly fractionated, whereas at high pH, RO permeates are enriched by 20 per thousand in 11B due to selective rejection of borate ion and preferential permeation of 11B-enriched boric acid through the membrane. The specific geochemical and isotopic fingerprints of SWRO provide a unique tool for tracing "man-made" fresh water as an emerging recharge component of natural water resources.

  10. Measurements of Ion Selective Containment on the RF Charge Breeder Device BRIC

    CERN Document Server

    Variale, Vincenzo; Batazova, Marina; Boggia, Antonio; Clauser, Tarcisio; Kuznetsov, Gennady I; Rainò, Antonio; Shiyankov, Sergey; Skarbo, Boris A; Valentino, Vincenzo; Verrone, Grazia

    2005-01-01

    The "charge state breeder" BRIC (BReeding Ion Charge) is based on an EBIS source and it is designed to accept Radioactive Ion Beam (RIB) with charge +1, in a slow injection mode, to increase their charge state up to +n. BRIC has been developed at the INFN section of Bari (Italy) during these last 3 years with very limited funds. Now, it has been assembled at the LNL (Italy) where are in progress the first tests as stand alone source. The new feature of BRIC, with respect to the classical EBIS, is given by the insertion, in the ion drift chamber, of a Radio Frequency (RF) Quadrupole aiming to filtering the unwanted elements and then making a more efficient containment of the wanted ions. In this contribution, the measurements of the selective effect on the ion charge state containement of the RF quadrupole field, applied on the ion chamber, will be reported and discussed. The ion charge state analisys of the ions trapped in BRIC seem confirm, as foreseen by simulation results carried out previously, that the s...

  11. 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.

  12. Selective detection of ferric ions by blue-green photoluminescent nitrogen-doped phenol formaldehyde resin polymer.

    Science.gov (United States)

    Zhang, Jia; Yuan, Yue; Yu, Zhi-Long; Yu, Aimin; Yu, Shu-Hong

    2014-09-24

    The smaller, the more fluorescent: The hydrothermal reaction of phenol with hexamethylenetetramine (HMT) leads to two morphologies of phenol formaldehyde resin (PFR), namely, bigger nanoparticles with feeble green fluorescence and smaller amorphous polymers with strong blue-green fluorescence. It reveals that both of them are doped with nitrogen, and the blue-green photoluminescent polymer is confirmed to sense ferric ion (Fe(3+) ) with high selectivity. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  13. Generation of High Quality Laser Accelerated Ion Beams

    OpenAIRE

    Esirkepov, T. Zh.; Bulanov, S. V.; Nishihara, K.; Tajima, T.; Pegoraro, F.; Khoroshkov, V. S.; Mima, K.; Daido, H.; Kato, Y.; Kitagawa, Y.; Nagai, K.; Sakabe, S.

    2002-01-01

    In order to achieve a high quality, i. e. monoergetic, intense ion beam, we propose the use of a double layer target. The first layer, at the target front, consists of high-Z atoms, while the second (rear) layer is a thin coating of low-Z atoms. The high quality proton beams from the double layer target, irradiated by an ultra-intense laser pulse, are demonstrated with three dimensional Particle-in-Cell simulations.

  14. Selective incarceration of caesium ions by Venus flytrap action of a flexible framework sulfide.

    Energy Technology Data Exchange (ETDEWEB)

    Ding, N.; Kanatzidis, M. G. (Materials Science Division); (Northwestern Univ.)

    2009-12-01

    The selective capture of Cs{sup +} from solution is relevant to the remediation of nuclear waste and remains a significant challenge. Here we describe a new framework composed of [(CH{sub 3}){sub 2}NH{sub 2}]{sup +} and [Ga{sub 2}Sb{sub 2}S{sub 7}]{sup 2-} layers, which are perforated with holes. Shape selectivity couples with framework flexibility, allowing the compound to respond to the ion-exchange process. The size, shape and flexibility of the holes allow Cs{sup +} ions in an aqueous solution to selectively pass through and enter the material via an ion-exchange process. Following capture, the structure dynamically closes its holes in a manner reminiscent of a Venus flytrap, which prevents the Cs{sup +} ions from leaching out. This process has useful implications in the separation science of Cs as it relates to the clean-up of nuclear waste. The dynamic response we describe here provides important insights for designing new materials for the selective removal of difficult-to-capture ions.

  15. Electrochemical activation and inhibition of neuromuscular systems through modulation of ion concentrations with ion-selective membranes

    Science.gov (United States)

    Song, Yong-Ak; Melik, Rohat; Rabie, Amr N.; Ibrahim, Ahmed M. S.; Moses, David; Tan, Ara; Han, Jongyoon; Lin, Samuel J.

    2011-12-01

    Conventional functional electrical stimulation aims to restore functional motor activity of patients with disabilities resulting from spinal cord injury or neurological disorders. However, intervention with functional electrical stimulation in neurological diseases lacks an effective implantable method that suppresses unwanted nerve signals. We have developed an electrochemical method to activate and inhibit a nerve by electrically modulating ion concentrations in situ along the nerve. Using ion-selective membranes to achieve different excitability states of the nerve, we observe either a reduction of the electrical threshold for stimulation by up to approximately 40%, or voluntary, reversible inhibition of nerve signal propagation. This low-threshold electrochemical stimulation method is applicable in current implantable neuroprosthetic devices, whereas the on-demand nerve-blocking mechanism could offer effective clinical intervention in disease states caused by uncontrolled nerve activation, such as epilepsy and chronic pain syndromes.

  16. Role of the electric field in selective ion filtration in nanostructures.

    Science.gov (United States)

    Park, Yong; Kim, Sueon; Jang, In Hyuk; Nam, Young Suk; Hong, Hiki; Choi, Dukhyun; Lee, Won Gu

    2016-02-21

    Nafion has received great attention as a proton conductor that can block negative ions. Here, we report the effect of a Nafion coating on an anodic aluminium oxide (AAO) nanoporous membrane on its function of ion rejection and filtering depending on the electric field. In our experiments, Nafion, once coated, was used to repel the negative ions (anions) from the coated surface, and then selectively allowed positive ions (cations) to pass through the nanopores in the presence of an electric field. To demonstrate the proof-of-concept validation, we coated Nafion solution onto the surface of AAO membranes with 20 nm nanopores average diameter at different solution concentration levels. Vacuum filtration methods for Nafion coating were vertically applied to the plane of an AAO membrane. An electric field was then applied to the upper surface of the Nafion-coated AAO membrane to investigate if ion rejection and filtering was affected by the presence of the electric field. Both anions and cations could pass through the AAO nanopores without an electric field applied. However, only cations could well pass through the AAO nanopores under an electric field, thus effectively blocking anions from passing through the nanopores. This result shows that ion filtration of electrons has been selectively performed while the system also works as a vital catalyst in reactivating Nafion via electrolysis. A saturated viscosity ratio of Nafion solution for the coating was also determined. We believe that this approach is potentially beneficial for better understanding the fundamentals of selective ion filtration in nanostructures and for promoting the use of nanostructures in potential applications such as ion-based water purification and desalination system at the nanoscale in a massively electrically integrated format.

  17. New development of laser ion source for highly charged ion beam production at Institute of Modern Physics (invited)

    Science.gov (United States)

    Zhao, H. Y.; Zhang, J. J.; Jin, Q. Y.; Liu, W.; Wang, G. C.; Sun, L. T.; Zhang, X. Z.; Zhao, H. W.

    2016-02-01

    A laser ion source based on Nd:YAG laser has been being studied at the Institute of Modern Physics for the production of high intensity high charge state heavy ion beams in the past ten years, for possible applications both in a future accelerator complex and in heavy ion cancer therapy facilities. Based on the previous results for the production of multiple-charged ions from a wide range of heavy elements with a 3 J/8 ns Nd:YAG laser [Zhao et al., Rev. Sci. Instrum. 85, 02B910 (2014)], higher laser energy and intensity in the focal spot are necessary for the production of highly charged ions from the elements heavier than aluminum. Therefore, the laser ion source was upgraded with a new Nd:YAG laser, the maximum energy of which is 8 J and the pulse duration can be adjusted from 8 to 18 ns. Since then, the charge state distributions of ions from various elements generated by the 8 J Nd:YAG laser were investigated for different experimental conditions, such as laser energy, pulse duration, power density in the focal spot, and incidence angle. It was shown that the incidence angle is one of the most important parameters for the production of highly charged ions. The capability of producing highly charged ions from the elements lighter than silver was demonstrated with the incidence angle of 10° and laser power density of 8 × 1013 W cm-2 in the focal spot, which makes a laser ion source complementary to the superconducting electron cyclotron resonance ion source for the future accelerator complex especially in terms of the ion beam production from some refractory elements. Nevertheless, great efforts with regard to the extraction of intense ion beams, modification of the ion beam pulse duration, and reliability of the ion source still need to be made for practical applications.

  18. New development of laser ion source for highly charged ion beam production at Institute of Modern Physics (invited).

    Science.gov (United States)

    Zhao, H Y; Zhang, J J; Jin, Q Y; Liu, W; Wang, G C; Sun, L T; Zhang, X Z; Zhao, H W

    2016-02-01

    A laser ion source based on Nd:YAG laser has been being studied at the Institute of Modern Physics for the production of high intensity high charge state heavy ion beams in the past ten years, for possible applications both in a future accelerator complex and in heavy ion cancer therapy facilities. Based on the previous results for the production of multiple-charged ions from a wide range of heavy elements with a 3 J/8 ns Nd:YAG laser [Zhao et al., Rev. Sci. Instrum. 85, 02B910 (2014)], higher laser energy and intensity in the focal spot are necessary for the production of highly charged ions from the elements heavier than aluminum. Therefore, the laser ion source was upgraded with a new Nd:YAG laser, the maximum energy of which is 8 J and the pulse duration can be adjusted from 8 to 18 ns. Since then, the charge state distributions of ions from various elements generated by the 8 J Nd:YAG laser were investigated for different experimental conditions, such as laser energy, pulse duration, power density in the focal spot, and incidence angle. It was shown that the incidence angle is one of the most important parameters for the production of highly charged ions. The capability of producing highly charged ions from the elements lighter than silver was demonstrated with the incidence angle of 10° and laser power density of 8 × 10(13) W cm(-2) in the focal spot, which makes a laser ion source complementary to the superconducting electron cyclotron resonance ion source for the future accelerator complex especially in terms of the ion beam production from some refractory elements. Nevertheless, great efforts with regard to the extraction of intense ion beams, modification of the ion beam pulse duration, and reliability of the ion source still need to be made for practical applications.

  19. Numerical Simulation of High Specific Impulse Ion Thruster Grid System

    Science.gov (United States)

    Nakayama, Yoshinori

    A high specific impulse ion thruster (HiIsp-IT) operated at a voltage of over 10 kV has been studied and the problems of direct ion impingement on the accelerating grid and of production and impingement of charge-exchange ions have been considered. In order to investigate these problems and to facilitate the grid systems design, a three-dimensional particle simulation code that employs an energy compensation method, a simplified pre-sheath definition method, a region sharing method was developed. This code also simulates the production and subsequent motion of charge-exchange ions. Using this code, results obtained quickly using a personal computer are shown to be in good agreement with experimental data associated with: the crossover impingement under low-beam-current condition and the star-shaped pattern of ion beam cross section as it passes through the accelerating grid. It argued that this code is a useful tool for rapid preliminary analysis and design of HiIsp-IT grid systems.

  20. Two-photon processes in highly charged ions

    Energy Technology Data Exchange (ETDEWEB)

    Jahrsetz, Thorsten

    2015-03-05

    Two-photon processes are atomic processes in which an atom interacts simultaneously with two photons. Such processes describe a wide range of phenomena, such as two-photon decay and elastic or inelastic scattering of photons. In recent years two-photon processes involving highly charged heavy ions have become an active area of research. Such studies do not only consider the total transition or scattering rates but also their angular and polarization dependence. To support such examinations in this thesis I present a theoretical framework to describe these properties in all two-photon processes with bound initial and final states and involving heavy H-like or He-like ions. I demonstrate how this framework can be used in some detailed studies of different two-photon processes. Specifically a detailed analysis of two-photon decay of H-like and He-like ions in strong external electromagnetic fields shows the importance of considering the effect of such fields for the physics of such systems. Furthermore I studied the elastic Rayleigh as well as inelastic Raman scattering by heavy H-like ions. I found a number of previously unobserved phenomena in the angular and polarization dependence of the scattering cross-sections that do not only allow to study interesting details of the electronic structure of the ion but might also be useful for the measurement of weak physical effects in such systems.

  1. Selective transport of ions and molecules across layer-by-layer assembled membranes of polyelectrolytes, p-sulfonato-calix[n]arenes and Prussian Blue-type complex salts.

    Science.gov (United States)

    Tieke, Bernd; Toutianoush, Ali; Jin, Wanqin

    2005-11-30

    Our recent studies in the field of ultrathin membranes prepared upon layer-by-layer assembly of various polyionic compounds such as polyelectrolytes, calixarenes and polyelectrolytes, and metal hexacyanoferrate salts such as Prussian Blue are reviewed. It is demonstrated that polyelectrolyte multilayers can be used (a) as nanofiltration and reverse osmosis membranes suitable for water softening and seawater desalination and (b) as molecular sieves and ion sieves for size-selective separation of neutral and charged aromatic compounds. Furthermore, hybrid membranes of p-sulfonato-calixarenes and cationic polyelectrolytes showing specific host-guest interactions with permeating ions are described. The membranes exhibit high selectivities for distinct metal ions. Finally, it is demonstrated that purely inorganic membranes of Prussian Blue (PB) and analogues can be prepared upon multiple sequential adsorption of transition metal cations and hexacyanoferrate anions. Due to the porous lattice of PB, the membranes are useful as ion filters able to separate cesium from sodium ions, for example.

  2. Development of intense high-energy noble gas ion beams from in-terminal ion injector of tandem accelerator using an ECR ion source

    Energy Technology Data Exchange (ETDEWEB)

    Matsuda, M., E-mail: matsuda.makoto@jaea.go.jp [Japan Atomic Energy Agency (JAEA), Tokai Research and Development Center, 2-4 Shirakata-shirane, Tokai, Naka, Ibaraki 319-1195 (Japan); Nakanoya, T.; Hanashima, S.; Takeuchi, S. [Japan Atomic Energy Agency (JAEA), Tokai Research and Development Center, 2-4 Shirakata-shirane, Tokai, Naka, Ibaraki 319-1195 (Japan)

    2011-10-21

    An ECRIS-based heavy ion injector was constructed in the high-voltage terminal of JAEA-Tokai Tandem Accelerator to develop new beam species of highly charged noble gas ions. This work was associated with a lot of development to operate the ion source on the 20UR Pelletron high voltage terminal in high pressure SF{sub 6} gas environment. Highly charged ions of N, O, Ne, Ar, Kr and Xe have been accelerated satisfactorily. Operating data integrated during many years long beam delivery service are summarized.

  3. Tunable catalytic activities and selectivities of metal ion doped TiO2 nanoparticles--oxidation of organic compounds.

    Science.gov (United States)

    Wang, Anqi; Jing, Huanwang

    2014-01-21

    A series of metal ion doped TiO2 nanoparticles (M-TiO2, M = Cr(3+), Mn(2+), Fe(3+), V(5+), Zn(2+), Ni(2+), Ag(+), Cu(2+) and Co(2+)) were prepared by a facile co-precipitation approach and characterized by means of ICP-AES, N2 adsorption-desorption isotherms, XRD, TEM and HRTEM. Their catalytic performance was investigated via the oxidation of organic compounds. The variation of metal ion species and doping contents allowed tuning the catalytic properties of the M-TiO2. Among them, the catalyst Cu-10 displayed excellent activity (97.5%) in the oxidation of styrene and the selectivity of benzaldehyde was as high as 99.4%. Surprisingly, the product distribution of styrene oxidation experienced a reverse trend over the Co-TiO2 catalysts with different doping amounts of cobalt ions: Co-10 was in favor of forming benzaldehyde (80.2% selectivity), in contrast with Co-15, which produced styrene oxide as the dominant product (84.7% selectivity). The M-TiO2 catalysts also showed catalytic activities for the oxidation of benzyl alcohol and toluene to generate chlorine-free benzaldehyde in excellent selectivities (>99%).

  4. Selectively accelerated lithium ion transport to silicon anodes via an organogel binder

    Science.gov (United States)

    Hwang, Chihyun; Cho, Yoon-Gyo; Kang, Na-Ri; Ko, Younghoon; Lee, Ungju; Ahn, Dongjoon; Kim, Ju-Young; Kim, Young-Jin; Song, Hyun-Kon

    2015-12-01

    Silicon, a promising high-capacity anode material of lithium ion batteries, suffers from its volume expansion leading to pulverization and low conductivities, showing capacity decay during cycling and low capacities at fast charging and discharging. In addition to popular active-material-modifying strategies, building lithium-ion-rich environments around silicon surface is helpful in enhancing unsatisfactory performances of silicon anodes. In this work, we accelerated lithium ion transport to silicon surface by using an organogel binder to utilize the electroactivity of silicon in a more efficient way. The cyanoethyl polymer (PVA-CN), characterized by high lithium ion transference number as well as appropriate elastic modulus with strong adhesion, enhanced cycle stability of silicon anodes with high coulombic efficiency even at high temperature (60 °C) as well as at fast charging/discharging rates.

  5. Selective removal of heavy metal ions by disulfide linked polymer networks

    Energy Technology Data Exchange (ETDEWEB)

    Ko, Dongah [Department of Environmental Engineering, Technical University of Denmark, Miljøvej 113, 2800 Kgs. Lyngby (Denmark); Lee, Joo Sung [Graduate School of EEWS, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141 (Korea, Republic of); Patel, Hasmukh A. [Department of Chemistry, Northwestern University, Evanston, IL 60208 (United States); Jakobsen, Mogens H. [Department of Micro and Nano technology, Technical University of Denmark, Ørsteds Plads, 345B, 2800 Kgs. Lyngby (Denmark); Hwang, Yuhoon [Department of Environmental Engineering, Seoul National University of Science and Technology, 232 Gongreung-ro, Nowon-gu, Seoul 01811 (Korea, Republic of); Yavuz, Cafer T. [Graduate School of EEWS, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141 (Korea, Republic of); Hansen, Hans Chr. Bruun [Department of Plant and Environmental Sciences, University of Copenhagen, Frederiksberg, Thorvaldsensvej 40, 1871 Frederiksberg C (Denmark); Andersen, Henrik R., E-mail: henrik@ndersen.net [Department of Environmental Engineering, Technical University of Denmark, Miljøvej 113, 2800 Kgs. Lyngby (Denmark)

    2017-06-15

    Highlights: • Disulfide/thiol polymer networks are promising as sorbent for heavy metals. • Rapid sorption and high Langmuir affinity constant (a{sub L}) for stormwater treatment. • Selective sorption for copper, cadmium, and zinc in the presence of calcium. • Reusability likely due to structure stability of disulfide linked polymer networks. - Abstract: Heavy metal contaminated surface water is one of the oldest pollution problems, which is critical to ecosystems and human health. We devised disulfide linked polymer networks and employed as a sorbent for removing heavy metal ions from contaminated water. Although the polymer network material has a moderate surface area, it demonstrated cadmium removal efficiency equivalent to highly porous activated carbon while it showed 16 times faster sorption kinetics compared to activated carbon, owing to the high affinity of cadmium towards disulfide and thiol functionality in the polymer network. The metal sorption mechanism on polymer network was studied by sorption kinetics, effect of pH, and metal complexation. We observed that the metal ions–copper, cadmium, and zinc showed high binding affinity in polymer network, even in the presence of competing cations like calcium in water.

  6. Highly antibacterial UHMWPE surfaces by implantation of titanium ions

    Science.gov (United States)

    Delle Side, D.; Nassisi, V.; Giuffreda, E.; Velardi, L.; Alifano, P.; Talà, A.; Tredici, S. M.

    2014-07-01

    The spreading of pathogens represents a serious threat for human beings. Consequently, efficient antimicrobial surfaces are needed in order to reduce risks of contracting severe diseases. In this work we present the first evidences of a new technique to obtain a highly antibacterial Ultra High Molecular Weight Polyethylene (UHMWPE) based on a non-stoichiometric titanium oxide coating, visible-light responsive, obtained through ion implantation.

  7. Structure of High Energy, Heavy Ions in Venus' Upper Ionosphere

    Science.gov (United States)

    Persson, Moa; Futaana, Yoshifumi; Nilsson, Hans; Stenberg Wieser, Gabriella; Hamrin, Maria; Fedorov, Andrei; Barabash, Stas

    2017-04-01

    The solar wind interacts with the atmosphere of Venus, and can reach directly down to the ionosphere. The interaction has previously been studied using the Pioneer Venus mission (PVO) and is now known to cause variations in the density in the ionosphere [Taylor et al., 1980], a transport of ions towards the night side [Knudsen et al., 1980], and an outflow of ions from the atmosphere [Barabash et al., 2007]. Measurements made by PVO showed that the main constituents of Venus ionosphere in the altitude range 150-400 km is the O+ and O2+ ions, where the former dominates from 180 km and higher, and the latter dominates from 180 km down to 150 km [Taylor et al., 1980]. New measurements, made by the Ion Mass Analyzer (IMA) onboard the Venus Express spacecraft, reveal the high-energy (10 eV to 15 keV) plasma characteristics in the ionosphere of Venus. Using the data collected during the low altitude (down to 130 km) pericentre passages during the aerobraking time period, we are able to extract the height profile of the total heavy ion content (O+ and O2+ ions) of Venus ionosphere. The results show two scale heights separated at 200 km; 10 km for 200 km. We interpret the results as two heavy ion components, namely, the O+ ions are dominant for >200 km, while the O2+ is dominant for methods of mass separation, to extract the two ion components of the scale height profiles, (O+ and O2+). First method is to use the moderate mass separation capabilities of the IMA instrument. The individual mass spectra are fitted by two Gaussian curves, representing O+ and O2+, derived from ground calibration information. The second method uses the energy spectrum, which sometimes has two discrete peaks. By assuming the same velocity for different components in the spacecraft reference frame (resulting in different energy for different masses), we can separate the composition. We will discuss the results of the obtained mass separated height profiles.

  8. Assessment of commercially available ion exchange materials for cesium removal from highly alkaline wastes

    Energy Technology Data Exchange (ETDEWEB)

    Brooks, K.P.; Kim, A.Y.; Kurath, D.E.

    1996-04-01

    Approximately 61 million gallons of nuclear waste generated in plutonium production, radionuclide removal campaigns, and research and development activities is stored on the Department of Energy`s Hanford Site, near Richland, Washington. Although the pretreatment process and disposal requirements are still being defined, most pretreatment scenarios include removal of cesium from the aqueous streams. In many cases, after cesium is removed, the dissolved salt cakes and supernates can be disposed of as LLW. Ion exchange has been a leading candidate for this separation. Ion exchange systems have the advantage of simplicity of equipment and operation and provide many theoretical stages in a small space. The organic ion exchange material Duolite{trademark} CS-100 has been selected as the baseline exchanger for conceptual design of the Initial Pretreatment Module (IPM). Use of CS-100 was chosen because it is considered a conservative, technologically feasible approach. During FY 96, final resin down-selection will occur for IPM Title 1 design. Alternate ion exchange materials for cesium exchange will be considered at that time. The purpose of this report is to conduct a search for commercially available ion exchange materials which could potentially replace CS-100. This report will provide where possible a comparison of these resin in their ability to remove low concentrations of cesium from highly alkaline solutions. Materials which show promise can be studied further, while less encouraging resins can be eliminated from consideration.

  9. 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)

  10. High resolution EUV spectroscopy of xenon ions with a compact electron beam ion trap

    Science.gov (United States)

    Ali, Safdar; Nakamura, Nobuyuki

    2017-09-01

    We performed high resolution extreme ultraviolet (EUV) spectroscopy measurements of highly charged xenon ions with a compact electron beam ion trap. The spectra were recorded with a flat-field grazing incidence spectrometer while varying the electron beam energy between 200 and 890 eV. We measured the wavelengths for several lines of Rh-like Xe9+ - Cd-like Xe6+ and Cu-like Xe25+- Se-like Xe20+ in the range of 150-200 Å with an uncertainty of 0.05 Å. Previously, most of these lines have been reported from EBITs with a wavelength uncertainty of 0.2 Å. Additionally, based on the electron beam energy dependence of the observed spectra we tentatively identified three new lines, which were reported as unidentified lines in the previous studies.

  11. [High-resolution patch-clamp technique based on feedback control of scanning ion conductance microscopy].

    Science.gov (United States)

    Yang, Xi; Liu, Xiao; Zhang, Xiao-Fan; Lu, Hu-Jie; Zhang, Yan-Jun

    2010-06-25

    The ion channels located on the cell fine structures play an important role in the physiological functions of cell membrane. However, it is impossible to achieve precise positioning on the nanometer scale cellular microstructures by conventional patch-clamp technique, due to the 200 nm resolution limit of optical microscope. To solve this problem, we have established a high-resolution patch-clamp technique, which combined commercial scanning ion conductance microscopy (SICM) and patch-clamp recording through a nanopipette probe, based on SICM feedback control. MDCK cells were used as observation object to test the capability of the technique. Firstly, a feedback controlled SICM nanopipette (approximately 150 MOmega) non-contactly scanned over a selected area of living MDCK cells monolayer to obtain high-resolution topographic images of microvilli and tight-junction microstructures on the MDCK cells monolayer. Secondly, the same nanopipette was non-contactly moved and precisely positioned over the microvilli or tight-junction microstructure under SICM feedback control. Finally, the SICM feedback control was switched off, the nanopipette slowly contacted with the cell membrane to get a patch-clamp giga-ohm sealing in the cell-attached patch-clamp configuration, and then performed ion channel recording as a normal patch-clamp electrode. The ion channel recordings showed that ion channels of microvilli microstructure opened at pipette holding potential of -100, -60, -40, 0, +40, +60, +100 mV (n=11). However, the opening of ion channels of tight-junction microstructure was not detected at pipette holding potential of -100, -40, 0, +40, +100 mV (n=9). These results suggest that our high-resolution patch-clamp technique can achieve accurate nanopipette positioning and nanometer scale high-resolution patch-clamp recording, which may provide a powerful tool to study the spatial distribution and functions of ion channel in the nanometer scale microstructures of living

  12. Magnetic fluctuations embedded in dipolarization inside geosynchronous orbit and their associated selective acceleration of O+ ions

    Science.gov (United States)

    Nosé, M.; Takahashi, K.; Keika, K.; Kistler, L. M.; Koga, K.; Koshiishi, H.; Matsumoto, H.; Shoji, M.; Miyashita, Y.; Nomura, R.

    2014-06-01

    We study magnetic fluctuations embedded in dipolarizations in the inner magnetosphere (a geocentric distance of ≤6.6 RE) and their associated ion flux changes, using the Engineering Test Satellite VIII and Active Magnetospheric Particle Tracer Explorers/CCE satellites. We select seven events of dipolarization that occur during the main phase of magnetic storms having a minimum value of the Dst index less than -40 nT. It is found that (1) all of the dipolarization events are accompanied by strong magnetic fluctuations with the major frequency close to the local O+ gyrofrequency; (2) the magnetic fluctuations appear with significant amplitude in the component nearly parallel to the local magnetic field; (3) the strong flux enhancement is seen in the energy range of 1-10 keV only for O+ ions. In terms of frequency and dominant components of the magnetic fluctuations, they are considered to be excited by the drift-driven electromagnetic ion cyclotron (EMIC) instability that is recently identified with the linear theory. We perform particle tracing for H+ and O+ ions in the electromagnetic fields modeled by the linear dispersion relation of the drift-driven EMIC instability. Results show that the O+ ions are accelerated to the energy range of 0.5-5 keV and undergo a significant modification of the spectral shape, while the H+ ions have no clear change of spectral shape, being consistent with the observations. We therefore suggest that the electromagnetic fluctuations associated with the dipolarizations can accelerate O+ ions locally and nonadiabatically in the inner magnetosphere. This selective acceleration of O+ ions may play a role in enhancing the O+ energy density in the storm time ring current.

  13. Liquid membrane ion-selective electrodes for potentiometric dosage of coper and nickel

    Directory of Open Access Journals (Sweden)

    MARIA PLENICEANY

    2005-02-01

    Full Text Available This paper presents experimental and theoretical data regarding the preparation and characterization of three liquid-membrane electrodes, which have not been mentioned in the specialized literature so far. The active substances, the solutions of which in nitrobenzene formed the membranes on a graphite rod, are simple complex combinations of Cu(II and Ni(II ions with an organic ligand belonging to the Schiff base class: N-[2-thienylmethilidene]-2-aminoethanol (TNAHE. The Cu2+ -selective and Ni2+ -selective electrodes were used to determine the copper and nickel ions in aqueous solutions, both by direct potentiometry and by potentiometric titration with EDTA. They were also used for the determination of Cu2+ and Ni2+ ions in industrial waters by direct potentiometry.

  14. Nanoneedle transistor-based sensors for the selective detection of intracellular calcium ions.

    Science.gov (United States)

    Son, Donghee; Park, Sung Young; Kim, Byeongju; Koh, Jun Tae; Kim, Tae Hyun; An, Sangmin; Jang, Doyoung; Kim, Gyu Tae; Jhe, Wonho; Hong, Seunghun

    2011-05-24

    We developed a nanoneedle transistor-based sensor (NTS) for the selective detection of calcium ions inside a living cell. In this work, a single-walled carbon nanotube-based field effect transistor (swCNT-FET) was first fabricated at the end of a glass nanopipette and functionalized with Fluo-4-AM probe dye. The selective binding of calcium ions onto the dye molecules altered the charge state of the dye molecules, resulting in the change of the source-drain current of the swCNT-FET as well as the fluorescence intensity from the dye. We demonstrated the electrical and fluorescence detection of the concentration change of intracellular calcium ions inside a HeLa cell using the NTS.

  15. Ion aggregation in high salt solutions. IV. Graph-theoretical analyses of ion aggregate structure and water hydrogen bonding network

    Science.gov (United States)

    Choi, Jun-Ho; Cho, Minhaeng

    2015-09-01

    Ions in high salt solutions form a variety of ion aggregates, from ion pairs to clusters and networks. Their influences on water hydrogen bonding (H-bonding) network structures have long been of great interest. Recently, we have shown that the morphological structures of ion aggregates can be analyzed by using a spectral graph analysis theory, where each ion cluster or ion network is represented by a properly defined graph with edges and vertices. Here, to further examine the network properties of ion aggregates and water H-bonding networks in high salt solutions, we consider a few representative graph-theoretical descriptors: clustering coefficient, minimum path length, global efficiency, and degree distribution of ion aggregates. From the molecular dynamics trajectories, these graph theoretical properties of ion aggregates and water structures in NaCl and kosmotropic solutions are calculated and shown to be strongly dependent on the two types of ion aggregate structures, i.e., ion cluster and ion network. Ion clusters in high NaCl solutions exhibit typical behaviors of scale free network. The corresponding graph theoretical properties of ion networks in high KSCN solutions are notably different from those of NaCl ion clusters and furthermore they are very similar to those of water hydrogen-bonding network. The present graph-theoretical analysis results indicate that the high solubility limits of KSCN and other ion-network-forming salts might originate from their ability to form a large scale morphological network that can be intertwined with co-existing water H-bonding network. Furthermore, it is shown that the graph-theoretical properties of water H-bonding network structures do not strongly depend on the nature of dissolved ions nor on the morphological structures of ion aggregates, indicating that water's H-bonding interaction and network-forming capability are highly robust. We anticipate that the present graph-theoretical analysis results of high salt

  16. Ion aggregation in high salt solutions. IV. Graph-theoretical analyses of ion aggregate structure and water hydrogen bonding network.

    Science.gov (United States)

    Choi, Jun-Ho; Cho, Minhaeng

    2015-09-14

    Ions in high salt solutions form a variety of ion aggregates, from ion pairs to clusters and networks. Their influences on water hydrogen bonding (H-bonding) network structures have long been of great interest. Recently, we have shown that the morphological structures of ion aggregates can be analyzed by using a spectral graph analysis theory, where each ion cluster or ion network is represented by a properly defined graph with edges and vertices. Here, to further examine the network properties of ion aggregates and water H-bonding networks in high salt solutions, we consider a few representative graph-theoretical descriptors: clustering coefficient, minimum path length, global efficiency, and degree distribution of ion aggregates. From the molecular dynamics trajectories, these graph theoretical properties of ion aggregates and water structures in NaCl and kosmotropic solutions are calculated and shown to be strongly dependent on the two types of ion aggregate structures, i.e., ion cluster and ion network. Ion clusters in high NaCl solutions exhibit typical behaviors of scale free network. The corresponding graph theoretical properties of ion networks in high KSCN solutions are notably different from those of NaCl ion clusters and furthermore they are very similar to those of water hydrogen-bonding network. The present graph-theoretical analysis results indicate that the high solubility limits of KSCN and other ion-network-forming salts might originate from their ability to form a large scale morphological network that can be intertwined with co-existing water H-bonding network. Furthermore, it is shown that the graph-theoretical properties of water H-bonding network structures do not strongly depend on the nature of dissolved ions nor on the morphological structures of ion aggregates, indicating that water's H-bonding interaction and network-forming capability are highly robust. We anticipate that the present graph-theoretical analysis results of high salt

  17. Nickel ions selectively inhibit lipopolysaccharide-induced interleukin-6 production by decreasing its mRNA stability.

    Directory of Open Access Journals (Sweden)

    Sanki Asakawa

    Full Text Available Nickel (Ni ions easily elute from many alloys and elicit inflammation and allergies. Previous studies have shown that infections due to the implantation of medical devices cause inflammation and enhance the elution of Ni ions (Ni²⁺. However, cross-talk between infection- and Ni²⁺-induced signaling pathways has not yet been elucidated in detail. In the present study, we investigated the effects of Ni2+ on the lipopolysaccharide (LPS-induced production of cytokines in a LPS-induced air pouch-type inflammation model in BALB/c mice and the murine macrophage cell line RAW264. We demonstrated that Ni²⁺ inhibited the LPS-induced production of interleukin (IL-6, but not that of tumor necrosis factor (TNF-α both in vivo and in vitro. This inhibitory effect was also observed with cobalt ion (Co²⁺, but not with chloride ion (Cl⁻, zinc ion (Zn²⁺, or palladium ion (Pd²⁺, and was highly selective to the production of IL-6. Ni²⁺ did not inhibit the activation of ERK1/2, p38 MAPK, or JNK. Although Ni²⁺ decreased IL-6 mRNA levels, it failed to inhibit the LPS-induced activation of the IL-6 promoter. An experiment using actinomycin D, a transcription inhibitor, revealed that Ni²⁺ decreased the stability of IL-6 mRNA. Moreover, Ni²⁺ inhibited the LPS-induced expression of Arid5a, but not regnase-1. These results demonstrated that Ni²⁺ may have selectively inhibited the LPS-induced production of IL-6 by decreasing the Arid5a-dependent stabilization of IL-6 mRNA.

  18. Electron impact ionization of highly charged lithiumlike ions

    Energy Technology Data Exchange (ETDEWEB)

    Wong, K L

    1992-10-01

    Electron impact ionization cross sections can provide valuable information about the charge-state and power balance of highly charged ions in laboratory and astrophysical plasmas. In the present work, a novel technique based on x-ray measurements has been used to infer the ionization cross section of highly charged lithiumlike ions on the Livermore electron beam ion trap. In particular, a correspondence is established between an observed x ray and an ionization event. The measurements are made at one energy corresponding to approximately 2.3 times the threshold energy for ionization of lithiumlike ions. The technique is applied to the transition metals between Z=22 (titanium, Ti[sup 19+]) and Z=26 (iron, Fe[sup 23+]) and to Z=56 (barium, Ba[sup 53+]). The results for the transition metals, which have an estimated 17-33% uncertainty, are in good overall agreement with a relativistic distorted-wave calculation. However, less good agreement is found for barium, which has a larger uncertainty. Methods for properly accounting for the polarization in the x-ray intensities and for inferring the charge-state abundances from x-ray observations, which were developed for the ionization measurements, as well as an x-ray model that assists in the proper interpretation of the data are also presented.

  19. f-Element Ion Chelation in Highly Basic Media - Final Report

    Energy Technology Data Exchange (ETDEWEB)

    Paine, R.T.

    2000-12-12

    A large body of data has been collected over the last fifty years on the chemical behavior of f-element ions. The ions undergo rapid hydrolysis reactions in neutral or basic aqueous solutions that produce poorly understood oxide-hydroxide species; therefore, most of the fundamental f-element solution chemistry has allowed synthetic and separations chemists to rationally design advanced organic chelating ligands useful for highly selective partitioning and separation of f-element ions from complex acidic solution matrices. These ligands and new examples under development allow for the safe use and treatment of solutions containing highly radioactive species. This DOE/EMSP project was undertaken to address the following fundamental objectives: (1) study the chemical speciation of Sr and lanthanide (Ln) ions in basic aqueous media containing classical counter anions found in waste matrices; (2) prepare pyridine N-oxide phosphonates and phosphonic acids that might act as selective chelator s for Ln ions in model basic pH waste streams; (3) study the binding of the new chelators toward Ln ions and (4) examine the utility of the chelators as decontamination and dissolution agents under basic solution conditions. The project has been successful in attacking selected aspects of the very difficult problems associated with basic pH solution f-element waste chemistry. In particular, the project has (1) shed additional light on the initial stages of Ln ion sol-gel-precipitate formulation under basic solution conditions; (2) generated new families of pyridine phosphonic acid chelators; (3) characterized the function of the chelators and (4) examined their utility as oxide-hydroxide dissolution agents. These findings have contributed significantly to an improved understanding of the behavior of Ln ions in basic media containing anions found in typical waste sludges as well as to the development of sludge dissolution agents. The new chelating reagents are easily made and could be

  20. A metal ion charged mixed matrix membrane for selective adsorption of hemoglobin

    NARCIS (Netherlands)

    Tetala, K.K.R.; Skrzypek, Katarzyna; Levisson, M.; Stamatialis, Dimitrios

    2013-01-01

    In this work, we developed a mixed matrix membrane by incorporating 20–40 μm size iminodiacetic acid modified immobeads within porous Ethylene vinyl alcohol (EVAL) polymer matrix. The MMM were charged with copper ions for selective adsorption of bovine hemoglobin in presence of bovine serum albumin.

  1. A metal ion charged mixed matrix membrane for selective adsorption of hemoglobin

    NARCIS (Netherlands)

    Tetala, K.K.R.; Skrzypek, K.; Levisson, M.; Stamatialis, D.F.

    2013-01-01

    In this work, we developed a mixed matrix membrane by incorporating 20–40 µm size iminodiacetic acid modified immobeads within porous Ethylene vinyl alcohol (EVAL) polymer matrix. The MMM were charged with copper ions for selective adsorption of bovine hemoglobin in presence of bovine serum albumin.

  2. Ion Selective Ceramics for Waste Separations. Input for Annual Accomplishments Report

    Energy Technology Data Exchange (ETDEWEB)

    Spoerke, Erik David [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States)

    2015-10-01

    This report discusses“Ion-Selective Ceramics for Waste Separations” which aims to develop an electrochemical approach to remove fission product waste (e.g., Cs+ ) from the LiCl-KCl molten salts used in the pyroprocessing of spent nuclear fuel.

  3. Biomimetic supercontainers for size-selective electrochemical sensing of molecular ions

    Science.gov (United States)

    Netzer, Nathan L.; Must, Indrek; Qiao, Yupu; Zhang, Shi-Li; Wang, Zhenqiang; Zhang, Zhen

    2017-04-01

    New ionophores are essential for advancing the art of selective ion sensing. Metal-organic supercontainers (MOSCs), a new family of biomimetic coordination capsules designed using sulfonylcalix[4]arenes as container precursors, are known for their tunable molecular recognition capabilities towards an array of guests. Herein, we demonstrate the use of MOSCs as a new class of size-selective ionophores dedicated to electrochemical sensing of molecular ions. Specifically, a MOSC molecule with its cavities matching the size of methylene blue (MB+), a versatile organic molecule used for bio-recognition, was incorporated into a polymeric mixed-matrix membrane and used as an ion-selective electrode. This MOSC-incorporated electrode showed a near-Nernstian potentiometric response to MB+ in the nano- to micro-molar range. The exceptional size-selectivity was also evident through contrast studies. To demonstrate the practical utility of our approach, a simulated wastewater experiment was conducted using water from the Fyris River (Sweden). It not only showed a near-Nernstian response to MB+ but also revealed a possible method for potentiometric titration of the redox indicator. Our study thus represents a new paradigm for the rational design of ionophores that can rapidly and precisely monitor molecular ions relevant to environmental, biomedical, and other related areas.

  4. Effect of π electrons on the detection of silver ions by ion-selective electrodes containing tripodal broom molecules as an ionophore.

    Science.gov (United States)

    Yamamoto, Chihiro; Seto, Hirokazu; Ohto, Keisuke; Kawakita, Hidetaka; Harada, Hiroyuki

    2011-01-01

    Tripodal "broom" molecule derivatives containing π electrons were used as ionophores of silver ion-selective electrodes. The ability of the electrodes to detect silver ions was evaluated using the Nernst equation. When allyl- and propargyl-type tripodal broom molecules, and a propargyl-type monopodal analog were used in the electrode, Nernstian responses for silver ions were observed, indicating that π electrons play an important role in the detection of silver ions. In the presence of interfering metal ions, the selectivity for silver ions was affected by the number and density of π electrons in the ionophore. The electrode containing the allyl-type tripodal broom molecule was used to accurately determine the concentration of glucosamine hydrochloride in a real sample.

  5. Synthesis and application of ion imprinting polymer coated magnetic multi-walled carbon nanotubes for selective adsorption of nickel ion

    Science.gov (United States)

    He, Junnan; Shang, Hongzhou; Zhang, Xing; Sun, Xiaoran

    2018-01-01

    A novel nickel ion imprinted polymers (IIPs) based on multi-walled carbon nanotubes (MWCNTs) were synthesized inverse emulsion system, using chitosan(CS) and acrylic acid as the functional monomers, Ni (II) as the template, and N' N-methylene bis-acrylamide as the cross-linker. The chemical structure and morphological feature of the IIPs were characterized by scanning electron microscopy (SEM), Thermogravimetry (TG), X-ray diffraction (XRD), and Fourier transform infrared spectrometer (FTIR). The studies indicated that the gel layer was well grafted on the surface of MWCNTs. Studies on the adsorption ability of the IIPs, by atomic absorption spectrophotometry, demonstrated that IIPs possessed excellent adsorption and selective ability towards Ni (II), fitting to pseudo second-order kinetic isotherms and with a maximum capacity of 19.86 mg/g, and selectivity factor of 13.09 and 4.42. The electrochemical performance of ion imprinting carbon paste electrode (CPE/IIPs) was characterized by Cyclic voltammetry (CV). Studies have shown that CPE/IIPs showed excellent electrochemical performance.

  6. Letter: High-mass capabilities of positive-ion and negative-ion direct analysis in real time mass spectrometry.

    Science.gov (United States)

    Gross, Jürgen H

    2016-01-01

    Of the ionic liquid 1-butyl-3-methylimidazolium (C(+)) tricyanomethide (A(-)) high-mass cluster ions of both positive ([C(n)A(n-1)](+)) and negative ([C(n-1)A(n)](-)) charge were generated and detected by direct analysis in real time (DART) Fourier transform ion cyclotron resonance (FT-ICR) mass spectrometry (MS). After optimization of the settings of the DART ionization source and of the mass analyzer ions of m/z values unprecedented in DART-MS were detected. Thus, the upper m/z limits of positive-ion and negative-ion DART- MS were substantially expanded. Negative-ion DART-MS delivered cluster ions up to [C(15)A(16)](-), m/z 3527 (nominal mass of monoisotopic ion), while positive-ion DART-MS even yielded ions up to [C(30)A(29)](+), m/z 6784. The identification of the cluster ions is supported by their accurate mass and exact mass differences corresponding to CA between adjacent cluster ion peaks.

  7. New progress of high current gasdynamic ion source (invited)

    Energy Technology Data Exchange (ETDEWEB)

    Skalyga, V., E-mail: skalyga@ipfran.ru; Sidorov, A.; Vodopyanov, A. [Institute of Applied Physics, Russian Academy of Sciences (IAP RAS), 46 Ul‘yanova St., 603950 Nizhny Novgorod (Russian Federation); Lobachevsky State University of Nizhny Novgorod (UNN), 23 Gagarina St., 603950 Nizhny Novgorod (Russian Federation); Izotov, I.; Golubev, S.; Razin, S. [Institute of Applied Physics, Russian Academy of Sciences (IAP RAS), 46 Ul‘yanova St., 603950 Nizhny Novgorod (Russian Federation); Tarvainen, O.; Koivisto, H.; Kalvas, T. [Department of Physics, University of Jyvaskyla, P.O. Box 35 (YFL), 40500 Jyvaskyla (Finland)

    2016-02-15

    The experimental and theoretical research carried out at the Institute of Applied Physics resulted in development of a new type of electron cyclotron resonance ion sources (ECRISs)—the gasdynamic ECRIS. The gasdynamic ECRIS features a confinement mechanism in a magnetic trap that is different from Geller’s ECRIS confinement, i.e., the quasi-gasdynamic one similar to that in fusion mirror traps. Experimental studies of gasdynamic ECRIS were performed at Simple Mirror Ion Source (SMIS) 37 facility. The plasma was created by 37.5 and 75 GHz gyrotron radiation with power up to 100 kW. High frequency microwaves allowed to create and sustain plasma with significant density (up to 8 × 10{sup 13} cm{sup −3}) and to maintain the main advantages of conventional ECRIS such as high ionization degree and low ion energy. Reaching such high plasma density relies on the fact that the critical density grows with the microwave frequency squared. High microwave power provided the average electron energy on a level of 50-300 eV enough for efficient ionization even at neutral gas pressure range of 10{sup −4}–10{sup −3} mbar. Gasdynamic ECRIS has demonstrated a good performance producing high current (100-300 mA) multi-charged ion beams with moderate average charge (Z = 4-5 for argon). Gasdynamic ECRIS has appeared to be especially effective in low emittance hydrogen and deuterium beams formation. Proton beams with current up to 500 emA and RMS emittance below 0.07 π ⋅ mm ⋅ mrad have been demonstrated in recent experiments.

  8. Modifications of gallium phosphide single crystals using slow highly charged ions and swift heavy ions

    Energy Technology Data Exchange (ETDEWEB)

    El-Said, A.S., E-mail: elsaid@kfupm.edu.sa [Physics Department, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia); Wilhelm, R.A.; Heller, R.; Akhmadaliev, Sh.; Schumann, E. [Institute of Ion Beam Physics and Materials Research, Helmholtz-Zentrum Dresden-Rossendorf, 01328 Dresden (Germany); Sorokin, M. [National Research Centre ’Kurchatov Institute’, Kurchatov Square 1, 123182 Moscow (Russian Federation); Facsko, S. [Institute of Ion Beam Physics and Materials Research, Helmholtz-Zentrum Dresden-Rossendorf, 01328 Dresden (Germany); Trautmann, C. [GSI Helmholtz Centre for Heavy Ion Research, 64291 Darmstadt (Germany); Technische Universität Darmstadt, 64289 Darmstadt (Germany)

    2016-09-01

    GaP single crystals were irradiated with slow highly charged ions (HCI) using 114 keV {sup 129}Xe{sup (33–40)+} and with various swift heavy ions (SHI) of 30 MeV I{sup 9+} and 374 MeV–2.2 GeV {sup 197}Au{sup 25+}. The irradiated surfaces were investigated by scanning force microscopy (SFM). The irradiations with SHI lead to nanohillocks protruding from the GaP surfaces, whereas no changes of the surface topography were observed after the irradiation with HCI. This result indicates that a potential energy above 38.5 keV is required for surface nanostructuring of GaP. In addition, strong coloration of the GaP crystals was observed after irradiation with SHI. The effect was stronger for higher energies. This was confirmed by measuring an increased extinction coefficient in the visible light region.

  9. Selective electrodiffusion of zinc ions in a Zrt-, Irt-like protein, ZIPB

    Energy Technology Data Exchange (ETDEWEB)

    Lin, W.; Fu, D.; Chai, J.; Love, J.

    2010-12-10

    All living cells need zinc ions to support cell growth. Zrt-, Irt-like proteins (ZIPs) represent a major route for entry of zinc ions into cells, but how ZIPs promote zinc uptake has been unclear. Here we report the molecular characterization of ZIPB from Bordetella bronchiseptica, the first ZIP homolog to be purified and functionally reconstituted into proteoliposomes. Zinc flux through ZIPB was found to be nonsaturable and electrogenic, yielding membrane potentials as predicted by the Nernst equation. Conversely, membrane potentials drove zinc fluxes with a linear voltage-flux relationship. Direct measurements of metal uptake by inductively coupled plasma mass spectroscopy demonstrated that ZIPB is selective for two group 12 transition metal ions, Zn{sup 2+} and Cd{sup 2+}, whereas rejecting transition metal ions in groups 7 through 11. Our results provide the molecular basis for cellular zinc acquisition by a zinc-selective channel that exploits in vivo zinc concentration gradients to move zinc ions into the cytoplasm.

  10. The study towards high intensity high charge state laser ion sources.

    Science.gov (United States)

    Zhao, H Y; Jin, Q Y; Sha, S; Zhang, J J; Li, Z M; Liu, W; Sun, L T; Zhang, X Z; Zhao, H W

    2014-02-01

    As one of the candidate ion sources for a planned project, the High Intensity heavy-ion Accelerator Facility, a laser ion source has been being intensively studied at the Institute of Modern Physics in the past two years. The charge state distributions of ions produced by irradiating a pulsed 3 J/8 ns Nd:YAG laser on solid targets of a wide range of elements (C, Al, Ti, Ni, Ag, Ta, and Pb) were measured with an electrostatic ion analyzer spectrometer, which indicates that highly charged ions could be generated from low-to-medium mass elements with the present laser system, while the charge state distributions for high mass elements were relatively low. The shot-to-shot stability of ion pulses was monitored with a Faraday cup for carbon target. The fluctuations within ±2.5% for the peak current and total charge and ±6% for pulse duration were demonstrated with the present setup of the laser ion source, the suppression of which is still possible.

  11. Advanced Electrodes for High Power Li-ion Batteries

    Directory of Open Access Journals (Sweden)

    Christian M. Julien

    2013-03-01

    Full Text Available While little success has been obtained over the past few years in attempts to increase the capacity of Li-ion batteries, significant improvement in the power density has been achieved, opening the route to new applications, from hybrid electric vehicles to high-power electronics and regulation of the intermittency problem of electric energy supply on smart grids. This success has been achieved not only by decreasing the size of the active particles of the electrodes to few tens of nanometers, but also by surface modification and the synthesis of new multi-composite particles. It is the aim of this work to review the different approaches that have been successful to obtain Li-ion batteries with improved high-rate performance and to discuss how these results prefigure further improvement in the near future.

  12. 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.

  13. Selective and Efficient Solvent Extraction of Copper(II Ions from Chloride Solutions by Oxime Extractants

    Directory of Open Access Journals (Sweden)

    Zahra Kaboli Tanha

    2016-06-01

    Full Text Available Oxime extractants 3-tert-butyl-2-hydroxy-5-methyl benzaldehyde oxime (HL1 and 3-tert-butyl-2-hydroxy-5-methoxy benzaldehyde oxime (HL2 were synthesized and characterized by conventional spectroscopic methods. Suitable lipophilic nature of the prepared extractants allowed examining the ability of these molecules for extraction-separation of copper from its mixture with normally associated metal ions by performing competitive extraction experiments of Cu(II, Co(II, Ni(II, Zn(II, Cd(II and Pb(II ions from chloride solutions. Both ligands transfer selectively the copper ions into dichloromethane by a cation exchange mechanism. Conventional log-log analysis and isotherm curves showed that Cu(II ions are extracted as the complexes with 1:2 metal to ligand ratio by both extractants. Verification of the effect of the organic diluent used in the extraction of copper ions by HL1 and HL2 demonstrated that the extraction efficiency varies as: dichloromethane ~ dichloroethane > toluene > xylene > ethylacetate. Time dependency investigation of the extraction processes revealed that the kinetics of the extraction of copper by HL2 is more rapid than that of HL1. The application of the ligands for extraction-separation of copper ions from leach solutions of cobalt and nickel-cadmium filter-cakes of a zinc production plants was evaluated.

  14. Gas-phase fluorescence excitation and emission spectroscopy of mass-selected trapped molecular ions.

    Science.gov (United States)

    Bian, Qunzhou; Forbes, Matthew W; Talbot, Francis O; Jockusch, Rebecca A

    2010-03-20

    A flexible interface to perform optical spectroscopic measurements on gaseous ions stored in a modified commercial quadrupole ion trap (QIT) mass spectrometer is described. The modifications made to the mass spectrometer did not adversely affect its operating characteristics. Gas-phase ions are produced using electrospray ionization, mass isolated and stored in the trapping mass spectrometer. The ions are subsequently irradiated with visible light from a tunable laser and dispersed fluorescence spectra are recorded simultaneously. Mass spectra are recorded after the irradiation period. This set-up allows us to track a range of possible outcomes upon photoexcitation of selected ions including fluorescence, photofragmentation and photodetachment of electrons. The experimental set-up is characterized using rhodamine 590, which is a methyl ester variant of rhodamine 6G. Fluorescence excitation and emission spectra of gaseous rhodamine 590 are measured and compared with solution-phase spectra. Excitation and emission maxima for the gaseous ions are found to lie at higher energy than for the solvated rhodamine 590. In addition, the gas-phase Stokes shift is significantly smaller than the solution-phase Stokes shift. The effects of several experimental parameters on the observed fluorescence signal are investigated, including laser power, relative number of ions, q(z) trapping parameter and buffer gas pressure. In addition to its use for the photophysical characterization of the intrinsic properties of ionic chromophores, this set-up may be used to investigate the properties of mass-selected, dye-labeled biomolecules, both alone and in well-defined complexes and clusters.

  15. Fluorous polymeric membranes for ionophore-based ion-selective potentiometry: how inert is Teflon AF?

    Science.gov (United States)

    Lai, Chun-Ze; Koseoglu, Secil S; Lugert, Elizabeth C; Boswell, Paul G; Rábai, József; Lodge, Timothy P; Bühlmann, Philippe

    2009-02-04

    Fluorous media are the least polar and polarizable condensed phases known. Their use as membrane materials considerably increases the selectivity and robustness of ion-selective electrodes (ISEs). In this research, a fluorous amorphous perfluoropolymer was used for the first time as a matrix for an ISE membrane. Electrodes for pH measurements with membranes composed of poly[4,5-difluoro-2,2-bis(trifluoromethyl)-1,3-dioxole]-co-poly(tetrafluoroethylene) (87% dioxole monomer content; known as Teflon AF2400) as polymer matrix, a linear perfluorooligoether as plasticizer, sodium tetrakis[3,5-bis(perfluorohexyl)phenyl]borate providing for ionic sites, and bis[(perfluorooctyl)propyl]-2,2,2-trifluoroethylamine as H+ ionophore were investigated. All electrodes had excellent potentiometric selectivities, showed Nernstian responses to H+ over a wide pH range, exhibited enhanced mechanical stability, and maintained their selectivity over at least 4 weeks. For membranes of low ionophore concentration, the polymer affected the sensor selectivity noticeably at polymer concentrations exceeding 15%. Also, the membrane resistance increased quite strongly at high polymer concentrations, which cannot be explained by the Mackie-Meares obstruction model. The selectivities and resistances depend on the polymer concentration because of a functional group associated with Teflon AF2400, with a concentration of one functional group per 854 monomer units of the polymer. In the fluorous environment of these membranes, this functional group binds to Na+, K+, Ca2+, and the unprotonated ionophore with binding constants of 10(3.5), 10(1.8), 10(6.8), and 10(4.4) M(-1), respectively. Potentiometric and spectroscopic evidence indicates that these functional groups are COOH groups formed by the hydrolysis of carboxylic acid fluoride (COF) groups originally present in Teflon AF2400. The use of higher ionophore concentrations removes the undesirable effect of these COOH groups almost completely

  16. Fluorous Polymeric Membranes for Ionophore-Based Ion-Selective Potentiometry: How Inert is Teflon AF?

    Science.gov (United States)

    Lai, Chun-Ze; Koseoglu, Secil S.; Lugert, Elizabeth C.; Boswell, Paul G.; Rábai, József; Lodge, Timothy P.; Bühlmann, Philippe

    2011-01-01

    Fluorous media are the least polar and polarizable condensed phases known. Their use as membrane materials considerably increases the selectivity and robustness of ion-selective electrodes (ISEs). In this research, a fluorous amorphous perfluoropolymer was used for the first time as a matrix for an ISE membrane. Electrodes for pH measurements with membranes composed of poly[4,5-difluoro-2,2-bis(trifluoromethyl)-1,3-dioxole]-co-poly(tetrafluoroethylene) (87% dioxole monomer content; known as Teflon AF2400) as polymer matrix, a linear perfluorooligoether as plasticizer, sodium tetrakis[3,5-bis(perfluorohexyl)phenyl]borate providing for ionic sites, and bis[(perfluorooctyl)propyl]-2,2,2-trifluoroethylamine as H+-ionophore were investigated. All electrodes had excellent potentiometric selectivities, showed Nernstian responses to H+ over a wide pH range, exhibited enhanced mechanical stability and maintained their selectivity over at least four weeks. For membranes of low ionophore concentration, the polymer affected the sensor selectivity noticeably at polymer concentrations exceeding 15%. Also, the membrane resistance increased quite strongly at high polymer concentrations, which cannot be explained by the Mackie–Meares obstruction model. The selectivities and resistances depend on the polymer concentration because of a functional group associated with Teflon AF2400, with a concentration of one functional group per 854 monomer units of the polymer. In the fluorous environment of these membranes, this functional group binds to Na+, K+, Ca2+, and the unprotonated ionophore with binding constants of 103.5, 101.8, 106.8 and 104.4 M−1, respectively. Potentiometric and spectroscopic evidence indicates that these functional groups are COOH groups formed by the hydrolysis of carboxylic acid fluoride (COF) groups originally present in Teflon AF2400. The use of higher ionophore concentrations removes the undesirable effect of these COOH groups almost completely

  17. Deep Reactive Ion Etching for High Aspect Ratio Microelectromechanical Components

    DEFF Research Database (Denmark)

    Jensen, Søren; Yalcinkaya, Arda Deniz; Jacobsen, S.

    2004-01-01

    A deep reactive ion etch (DRIE) process for fabrication of high aspect ratio trenches has been developed. Trenches with aspect ratios exceeding 20 and vertical sidewalls with low roughness have been demonstrated. The process has successfully been used in the fabrication of silicon-on-insulator (SOI......) released comb drive based resonators and tunable capacitors for MEMS applications. Brief characterizations of the devices are presented....

  18. Progress in quantum electrodynamics theory of highly charged ions

    OpenAIRE

    Volotka, A. V.; Glazov, D. A.; Plunien, G.; Shabaev, V. M.

    2013-01-01

    Recent progress in quantum electrodynamics (QED) calculations of highly charged ions is reviewed. The theoretical predictions for the binding energies, the hyperfine splittings, and the g factors are presented and compared with available experimental data. Special attention is paid to tests of bound-state QED at strong field regime. Future prospects for tests of QED at the strongest electric and magnetic fields as well as for determination of the fine structure constant and the nuclear magnet...

  19. Ionophore-based ion-selective optical nanosensors operating in exhaustive sensing mode.

    Science.gov (United States)

    Xie, Xiaojiang; Zhai, Jingying; Crespo, Gastón A; Bakker, Eric

    2014-09-02

    Ion selective optical sensors are typically interrogated under conditions where the sample concentration is not altered during measurement. We describe here an alternative exhaustive detection mode for ion selective optical sensors. This exhaustive sensor concept is demonstrated with ionophore-based nanooptodes either selective for calcium or the polycationic heparin antidote protamine. In agreement with a theoretical treatment presented here, linear calibration curves were obtained in the exhaustive detection mode instead of the sigmoidal curves for equilibrium-based sensors. The response range can be tuned by adjusting the nanosensor loading. The nanosensors showed average diameters of below 100 nm and the sensor response was found to be dramatically faster than that for film-based optodes. Due to the strong binding affinity of the exhaustive nanosensors, total calcium concentration in human blood plasma was successfully determined. Optical determination of protamine in human blood plasma using the exhaustive nanosensors was attempted, but was found to be less successful.

  20. Selective adsorption of Pb (II) over the zinc-based MOFs in aqueous solution-kinetics, isotherms, and the ion exchange mechanism.

    Science.gov (United States)

    Wang, Lei; Zhao, Xinhua; Zhang, Jinmiao; Xiong, Zhenhu

    2017-06-01

    Two series of metal-organic frameworks (MOFs) with similar formula units but different central metal ions (M) or organic linkers (L), M-BDC (BDC = terephthalate, M = Zn, Zr, Cr, or Fe), or Zn-L (L = imidazolate-2-methyl, BDC, BDC-NH 2 ), were prepared and employed as the receptors for adsorption lead ions. It was found that the Zn-BDC exhibited a much higher adsorption capacity than the other M-BDC series with various metal ions which have very closely low capacities at same conditions. Furthermore, the Zn-L (L = imidazolate-2-methyl, BDC, BDC-NH 2 ) still have highly efficient adsorption capacity of lead ions, although the adsorption capacity varies with different ligand, as well as the adsorption rate and the equilibrium pH of the solution. This significant high adsorption over Zn-L, different from other M-BDC series with various metal ions (Zr, Cr, or Fe), can be explained by ion exchange between the central metal ions of Zn-L and lead ion in solution. Based on the analysis of FT-IR, X-ray diffraction pattern, the nitrogen adsorption isotherms, the zeta potentials, and the results, a plausible adsorption mechanism is proposed. When equivalent Zn-L were added to equal volume of aqueous solution with different concentration of lead ion, the content of zinc ion in the solution increases with the increase of the initial concentration of lead ions. The new findings could provide a potential way to fabricate new metal organic frameworks with high and selective capacities of the heavy metal ions.

  1. Ion transport through lipid bilayers by synthetic ionophores: modulation of activity and selectivity.

    Science.gov (United States)

    De Riccardis, Francesco; Izzo, Irene; Montesarchio, Daniela; Tecilla, Paolo

    2013-12-17

    The ion-coupled processes that occur in the plasma membrane regulate the cell machineries in all the living organisms. The details of the chemical events that allow ion transport in biological systems remain elusive. However, investigations of the structure and function of natural and artificial transporters has led to increasing insights about the conductance mechanisms. Since the publication of the first successful artificial system by Tabushi and co-workers in 1982, synthetic chemists have designed and constructed a variety of chemically diverse and effective low molecular weight ionophores. Despite their relative structural simplicity, ionophores must satisfy several requirements. They must partition in the membrane, interact specifically with ions, shield them from the hydrocarbon core of the phospholipid bilayer, and transport ions from one side of the membrane to the other. All these attributes require amphipathic molecules in which the polar donor set used for ion recognition (usually oxygens for cations and hydrogen bond donors for anions) is arranged on a lipophilic organic scaffold. Playing with these two structural motifs, donor atoms and scaffolds, researchers have constructed a variety of different ionophores, and we describe a subset of interesting examples in this Account. Despite the ample structural diversity, structure/activity relationships studies reveal common features. Even when they include different hydrophilic moieties (oxyethylene chains, free hydroxyl, etc.) and scaffolds (steroid derivatives, neutral or polar macrocycles, etc.), amphipathic molecules, that cannot span the entire phospholipid bilayer, generate defects in the contact zone between the ionophore and the lipids and increase the permeability in the bulk membrane. Therefore, topologically complex structures that span the entire membrane are needed to elicit channel-like and ion selective behaviors. In particular the alternate-calix[4]arene macrocycle proved to be a versatile

  2. Fabrication of an "ion-imprinting" dual-emission quantum dot nanohybrid for selective fluorescence turn-on and ratiometric detection of cadmium ions.

    Science.gov (United States)

    Wang, Jing; Jiang, Chenxing; Wang, Xiaoqi; Wang, Ligeng; Chen, Aimin; Hu, Jun; Luo, Zhihui

    2016-10-21

    In this work, we have fabricated a new dual-emission quantum dot (QD) nanohybrid for fluorescence ratiometric determination of cadmium ions (Cd 2+ ) in water samples, where the "turn-on" model and "ion-imprinting" technique were incorporated simultaneously. The nanohybrid probe was composed of green-emitting CdSe QDs covalently linked onto the surface of silica nanoparticles embedded with red-emitting CdTe QDs. The chemical etching of ethylene diamine tetraacetic acid (EDTA) at the surface produced specific Cd 2+ recognition sites and quenched the green fluorescence of outer CdSe QDs. Upon exposure to different amounts of Cd 2+ , the green fluorescence was gradually restored, whereas the inner red fluorescence remained constant. As a consequence, an obviously distinguishable fluorescence color variation (from red to green) of the probe solution was observed. Under the optimized conditions, the developed ratiometric sensor displayed a linear response range from 0.1 to 9 μM with a detection limit of 25 nM (S/N = 3) for Cd 2+ , which could offer an alternative sensing approach for the highly sensitive and selective detection of heavy metal ions.

  3. Free calcium ions in neurones of Helix aspersa measured with ion-selective micro-electrodes.

    Science.gov (United States)

    Alvarez-Leefmans, F J; Rink, T J; Tsien, R Y

    1981-01-01

    1. Intracellular free calcium concentration, [Ca2+]i, was measured in giant neurones of the sub-oesophageal ganglia of Helix aspersa, using Ca-selective micro-electrodes containing a PVC-gelled, neutral-ligand sensor. 2. In calibration solutions the electrodes had a virtually ideal, Nernstian, response down to 1 microM-Ca2+ in the presence of 0.125 M-K+, 18-24 mV from 1 to 0.1 microM-Ca2+ and 8-14 mV from 0.1 to 0.01 microM-Ca2+. Interference from H+ and Mg2+ was negligible. The small response to Na+ at sub-micromolar Ca2+ was taken into account, when necessary, in measurement of [Ca2+]i. 3. Measurements of basal [Ca2+]i were made in ganglia from animals kept only a few weeks in captivity, in a bathing solution equilibrated with air and containing 2 mM-Ca2+. In thirteen measurements from impalements which met stringent criteria for electrode performance and cell viability, the mean basal pCa (--log10[Ca2+]) was 6.77 +/- 0.07 (S.E.), corresponding to a mean free Ca2+ concentration of 0.17 microM. 4. The basal [Ca2+]i in neurones from a group of snails kept hibernating for several months was higher, mean pCa 6.15, for ganglia handled in 2 mM-Ca2+ solution. 5. Intracellular injections of Ca2+ or EGTA raised and lowered, respectively, the indicated basal [Ca2+]i, showing that the electrodes responded appropriately inside the cells and that unknown or untested components of cytoplasm were not significantly interfering with the Ca-sensor. 6. Altering the external Ca2+ concentration between 0.1 and 10 mM usually produced only small, +/- 0.1 pCa units, changes in basal [Ca2+]i of satisfactorily impaled, quiescent cells. 7. In cell 1F, which has repetitive spikes with a substantial Ca current, changes in Ca gradient or blockade of voltage-dependent Ca channels sometimes markedly altered [Ca2+]i, showing that Ca entry with the spikes was elevating [Ca2+]i. 8. Replacing external Na+ with Li+ or bis(2-hydroxyethyl)dimethylammonium had little effect on [Ca2+]i. 9. Elevating CO2

  4. Selective removal of arsenic and monovalent ions from brackish water reverse osmosis concentrate.

    Science.gov (United States)

    Xu, Pei; Capito, Marissa; Cath, Tzahi Y

    2013-09-15

    Concentrate disposal and management is a considerable challenge for the implementation of desalination technologies, especially for inland applications where concentrate disposal options are limited. This study has focused on selective removal of arsenic and monovalent ions from brackish groundwater reverse osmosis (RO) concentrate for beneficial use and safe environmental disposal using in situ and pre-formed hydrous ferric oxides/hydroxides adsorption, and electrodialysis (ED) with monovalent permselective membranes. Coagulation with ferric salts is highly efficient at removing arsenic from RO concentrate to meet a drinking water standard of 10 μg/L. The chemical demand for ferric chloride however is much lower than ferric sulfate as coagulant. An alternative method using ferric sludge from surface water treatment plant is demonstrated as an efficient adsorbent to remove arsenic from RO concentrate, providing a promising low cost, "waste treat waste" approach. The monovalent permselective anion exchange membranes exhibit high selectivity in removing monovalent anions over di- and multi-valent anions. The transport of sulfate and phosphate through the anion exchange membranes was negligible over a broad range of electrical current density. However, the transport of divalent cations such as calcium and magnesium increases through monovalent permselective cation exchange membranes with increasing current density. Higher overall salt concentration reduction is achieved around limiting current density while higher normalized salt removal rate in terms of mass of salt per membrane area and applied energy is attained at lower current density because the energy unitization efficiency decreases at higher current density. Copyright © 2013 Elsevier B.V. All rights reserved.

  5. Coulomb crystals in a cryogenic Paul trap for sympathetic cooling of molecular ions and highly charged ions

    Science.gov (United States)

    Windberger, A.; Schwarz, M.; Versolato, O. O.; Baumann, T.; Bekker, H.; Schmöger, L.; Hansen, A. K.; Gingell, A. D.; Klosowski, L.; Kristensen, S.; Schmidt, P. O.; Ullrich, J.; Drewsen, M.; Crespo López-Urrutia, J. R.

    2013-03-01

    Electron beam ion traps used for spectroscopy of highly charged ions (HCI) produce a deep trapping potential leading to high temperatures of the stored ions, and thus limiting the achievable spectral resolution. A novel device at the Max-Planck-Institut für Kernphysik, the Cryogenic linear Paul Trap Experiment (CryPTEx), attached to an electron beam ion trap, provides a new experimental platform to overcome these limitations. The trap assembly operates at a temperature of 4 K and offers optical access for quantum manipulation and imaging of the trapped ions. Since forbidden optical transitions in HCI do not support direct laser cooling, sympathetic cooling with Coulomb crystals of singly charged ions such as Be+ or Mg+ will be applied in order to reach the natural linewidth of optical forbidden transitions in HCI of interest. With the added advantage of long ion trapping times resulting from residual gas pressures of H2 at 4 K below 10-15 mbar, CryPTEx has been commissioned in collaboration with the Ion Trap Group in Århus using rovibrationally cooled MgH+ ions. Strong suppression of the black body radiation at the trap center, ion storage times of about 28 hours, and largely enhanced population of the rovibrational ground state were achieved.

  6. A study of thermaů decomposition and combustion products of disposable polyethylene terephtalate plastic using high resolution fourier transform infrared spectroscopy, selected ion flow tube mass spectrometry and gas chromatography mass spectrometry

    Czech Academy of Sciences Publication Activity Database

    Sovová, Kristýna; Ferus, Martin; Matulková, Irena; Španěl, Patrik; Dryahina, Kseniya; Dvořák, O.; Civiš, Svatopluk

    2008-01-01

    Roč. 106, 9-10 (2008), s. 1205-1214 ISSN 0026-8976 R&D Projects: GA AV ČR IAA400400705; GA ČR GA202/06/0776 Institutional research plan: CEZ:AV0Z40400503 Keywords : polyethylene terephtalate (PET) * combustion * high resolution FTIR spectroscopy * GC-MS * SIFT-MS Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 1.478, year: 2008

  7. Correlation of precursor and product ions in single-stage high resolution mass spectrometry. A tool for detecting diagnostic ions and improving the precursor elemental composition elucidation.

    Science.gov (United States)

    Borràs, S; Kaufmann, A; Companyó, R

    2013-04-15

    Monitoring of common diagnostic fragments is essential for recognizing molecules which are members of a particular compound class. Up to now, unit resolving tandem quadrupole mass spectrometers, operating in the precursor ion scan mode, have been typically used to perform such analysis. By means of high-resolution mass spectrometry (HRMS) a much more sensitive and selective detection can be achieved. However, using a single-stage HRMS instrument, there is no unequivocal link to the corresponding precursor ion, since such instrumentation does not permit a previous precursor selection. Thus, to address this limitation, an in silico approach to locate precursor ions, based on diagnostic fragments, was developed. Implemented as an Excel macro, the algorithm rapidly assembles and surveys exact mass data to provide a list of feasible precursor candidates according to the correlation of the chromatographic peak shape profile and other additional filtering criteria (e.g. neutral losses and isotopes). The macro was tested with two families of veterinary drugs, sulfonamides and penicillins, which are known to yield diagnostic product ions when fragmented. Data sets obtained from different food matrices (fish and liver), both at high and low concentration of the target compounds, were investigated in order to evaluate the capabilities and limitations of the reported approach. Finally, other possible applications of this technique, such as the elucidation of elemental compositions based on product ions and corresponding neutral losses, were also presented and discussed. Copyright © 2013 Elsevier B.V. All rights reserved.

  8. A high resolution ion microscope for cold atoms

    Science.gov (United States)

    Stecker, Markus; Schefzyk, Hannah; Fortágh, József; Günther, Andreas

    2017-04-01

    We report on an ion-optical system that serves as a microscope for ultracold ground state and Rydberg atoms. The system is designed to achieve a magnification of up to 1000 and a spatial resolution in the 100 nm range, thereby surpassing many standard imaging techniques for cold atoms. The microscope consists of four electrostatic lenses and a microchannel plate in conjunction with a delay line detector in order to achieve single particle sensitivity with high temporal and spatial resolution. We describe the design process of the microscope including ion-optical simulations of the imaging system and characterize aberrations and the resolution limit. Furthermore, we present the experimental realization of the microscope in a cold atom setup and investigate its performance by patterned ionization with a structure size down to 2.7 μm. The microscope meets the requirements for studying various many-body effects, ranging from correlations in cold quantum gases up to Rydberg molecule formation.

  9. Cern academic training programme 2011: Selected Topics in the Physics of Heavy Ion Collisions

    CERN Multimedia

    PH Department

    2011-01-01

    LECTURE SERIES 14, 15 & 16 March 2011 Selected Topics in the Physics of Heavy Ion Collisions 11:00-12:00 - Bldg. 222-R-001 - Filtration Plant In these lectures, I discuss some classes of measurements accessible in heavy ion collisions at the LHC. How can these observables be measured, to what extent can they be calculated, and what do they tell us about the dense mesoscopic system created during the collision? In the first lecture, I shall focus in particular on measurements that constrain the spatio-temporal picture of the collisions and that measure centrality, orientations and extensions. In the subsequent lectures, I then discuss on how classes of measurements allow one to characterize collective phenomena, and to what extent these measurements can constrain the properties of matter produced in heavy ion collisions. Organiser: Maureen Prola-Tessaur/PH-EDU  

  10. Three-Dimensional Ionic Covalent Organic Frameworks for Rapid, Reversible, and Selective Ion Exchange.

    Science.gov (United States)

    Li, Zonglong; Li, Hui; Guan, Xinyu; Tang, Junjie; Yusran, Yusran; Li, Zhan; Xue, Ming; Fang, Qianrong; Yan, Yushan; Valtchev, Valentin; Qiu, Shilun

    2017-12-13

    Covalent organic frameworks (COFs) have emerged as functional materials for various potential applications. However, the availability of three-dimensional (3D) COFs is still limited, and nearly all of them exhibit neutral porous skeletons. Here we report a general strategy to design porous positively charged 3D ionic COFs by incorporation of cationic monomers in the framework. The obtained 3D COFs are built of 3-fold interpenetrated diamond net and show impressive surface area and CO2 uptakes. The ion-exchange ability of 3D ionic COFs has been highlighted by reversible removal of nuclear waste model ions and excellent size-selective capture for anionic pollutants. This research thereby provides a new perspective to explore 3D COFs as a versatile type of ion-exchange materials.

  11. Real-time measurement of peroxyacetyl nitrate using selected ion flow tube mass spectrometry.

    Science.gov (United States)

    Hastie, Donald R; Gray, John; Langford, Vaughan S; Maclagan, Robert G A R; Milligan, Daniel B; McEwan, Murray J

    2010-02-01

    The on-line detection of gaseous peroxyacetyl nitrate (PAN) using selected ion flow tube mass spectrometry (SIFT-MS) has been investigated using a synthetic sample of PAN in air at a humidity of approximately 30%. Using the H(3)O(+) reagent ion, signals due to PAN at m/z 122, 77 and 95 have been identified. These correspond to protonated PAN, protonated peractetic acid and its water cluster, respectively. These products and their energetics have been probed through quantum mechanical calculations. The rate coefficient of H(3)O(+) has been estimated to be 4.5 x 10(-9) cm(3) s(-1), leading to a PAN sensitivity of 138 cps/ppbv. This gives a limit of detection of 20 pptv in 10 s using the [M+H](+) ion of PAN at m/z 122. Copyright 2010 John Wiley & Sons, Ltd.

  12. Structural plasticity and dynamic selectivity of acid-sensing ion channel-spider toxin complexes

    Energy Technology Data Exchange (ETDEWEB)

    Baconguis, Isabelle; Gouaux, Eric [Oregon HSU

    2012-07-29

    Acid-sensing ion channels (ASICs) are voltage-independent, amiloride-sensitive channels involved in diverse physiological processes ranging from nociception to taste. Despite the importance of ASICs in physiology, we know little about the mechanism of channel activation. Here we show that psalmotoxin activates non-selective and Na+-selective currents in chicken ASIC1a at pH7.25 and 5.5, respectively. Crystal structures of ASIC1a–psalmotoxin complexes map the toxin binding site to the extracellular domain and show how toxin binding triggers an expansion of the extracellular vestibule and stabilization of the open channel pore. At pH7.25 the pore is approximately 10Å in diameter, whereas at pH5.5 the pore is largely hydrophobic and elliptical in cross-section with dimensions of approximately 5 by 7Å, consistent with a barrier mechanism for ion selectivity. These studies define mechanisms for activation of ASICs, illuminate the basis for dynamic ion selectivity and provide the blueprints for new therapeutic agents.

  13. Direct numerical simulation of current-induced convection near an ion-selective surface

    Science.gov (United States)

    Druzgalski, Clara; Andersen, Mathias B.; Mani, Ali

    2012-11-01

    Understanding fundamentals of electrokinetic transport and fluid flow phenomena near ion-selective surfaces provides insight to improve systems such as electrodialysis for water deionization. The work of Rubinstein and Zaltzman [e.g. Phys Rev E 62, 2238 (2000)] have clarified qualitative aspects of how development of current-induced space-charge layers near ion-selective surfaces can lead to the onset of electro-osmotic instabilities. We expand on this work through multidimensional numerical simulation of the full nonlinear Poisson-Nernst-Planck and Navier-Stokes equations with ideally selective membrane boundary conditions. Our numerical scheme is optimized by exploiting the periodicity in the system parallel to the ion-selective surface, using a spectral method in these coordinates. In the wall normal direction a finite difference approach accurately captures the strongly nonlinear nested boundary layer structure. Our numerical scheme fully resolves the concentration profiles throughout the system including the numerically stiff electric double layer and extended space charge layer. Our simulations enable prediction of the full continuous current versus voltage curves showing overlimiting current without resorting to any adjustable parameter.

  14. Ion beam enhancement in magnetically insulated ion diodes for high-intensity pulsed ion beam generation in non-relativistic mode

    Energy Technology Data Exchange (ETDEWEB)

    Zhu, X. P. [Key Laboratory of Materials Modification by Laser, Ion, and Electron Beams, Ministry of Education, Dalian University of Technology, Dalian 116024 (China); Surface Engineering Laboratory, School of Materials Science and Engineering, Dalian University of Technology, Dalian 116024 (China); Zhang, Z. C.; Lei, M. K., E-mail: surfeng@dlut.edu.cn [Surface Engineering Laboratory, School of Materials Science and Engineering, Dalian University of Technology, Dalian 116024 (China); Pushkarev, A. I. [Surface Engineering Laboratory, School of Materials Science and Engineering, Dalian University of Technology, Dalian 116024 (China); Laboratory of Beam and Plasma Technology, High Technologies Physics Institute, Tomsk Polytechnic University, 30, Lenin Ave, 634050 Tomsk (Russian Federation)

    2016-01-15

    High-intensity pulsed ion beam (HIPIB) with ion current density above Child-Langmuir limit is achieved by extracting ion beam from anode plasma of ion diodes with suppressing electron flow under magnetic field insulation. It was theoretically estimated that with increasing the magnetic field, a maximal value of ion current density may reach nearly 3 times that of Child-Langmuir limit in a non-relativistic mode and close to 6 times in a highly relativistic mode. In this study, the behavior of ion beam enhancement by magnetic insulation is systematically investigated in three types of magnetically insulated ion diodes (MIDs) with passive anode, taking into account the anode plasma generation process on the anode surface. A maximal enhancement factor higher than 6 over the Child-Langmuir limit can be obtained in the non-relativistic mode with accelerating voltage of 200–300 kV. The MIDs differ in two anode plasma formation mechanisms, i.e., surface flashover of a dielectric coating on the anode and explosive emission of electrons from the anode, as well as in two insulation modes of external-magnetic field and self-magnetic field with either non-closed or closed drift of electrons in the anode-cathode (A-K) gap, respectively. Combined with ion current density measurement, energy density characterization is employed to resolve the spatial distribution of energy density before focusing for exploring the ion beam generation process. Consistent results are obtained on three types of MIDs concerning control of neutralizing electron flows for the space charge of ions where the high ion beam enhancement is determined by effective electron neutralization in the A-K gap, while the HIPIB composition of different ion species downstream from the diode may be considerably affected by the ion beam neutralization during propagation.

  15. High capacity anode materials for lithium ion batteries

    Science.gov (United States)

    Lopez, Herman A.; Anguchamy, Yogesh Kumar; Deng, Haixia; Han, Yongbon; Masarapu, Charan; Venkatachalam, Subramanian; Kumar, Suject

    2015-11-19

    High capacity silicon based anode active materials are described for lithium ion batteries. These materials are shown to be effective in combination with high capacity lithium rich cathode active materials. Supplemental lithium is shown to improve the cycling performance and reduce irreversible capacity loss for at least certain silicon based active materials. In particular silicon based active materials can be formed in composites with electrically conductive coatings, such as pyrolytic carbon coatings or metal coatings, and composites can also be formed with other electrically conductive carbon components, such as carbon nanofibers and carbon nanoparticles. Additional alloys with silicon are explored.

  16. High throughput materials research and development for lithium ion batteries

    Directory of Open Access Journals (Sweden)

    Parker Liu

    2017-09-01

    Full Text Available Development of next generation batteries requires a breakthrough in materials. Traditional one-by-one method, which is suitable for synthesizing large number of sing-composition material, is time-consuming and costly. High throughput and combinatorial experimentation, is an effective method to synthesize and characterize huge amount of materials over a broader compositional region in a short time, which enables to greatly speed up the discovery and optimization of materials with lower cost. In this work, high throughput and combinatorial materials synthesis technologies for lithium ion battery research are discussed, and our efforts on developing such instrumentations are introduced.

  17. Highly sensitive vacuum ion pump current measurement system

    Science.gov (United States)

    Hansknecht, John Christopher [Williamsburg, VA

    2006-02-21

    A vacuum system comprising: 1) an ion pump; 2) power supply; 3) a high voltage DC--DC converter drawing power from the power supply and powering the vacuum pump; 4) a feedback network comprising an ammeter circuit including an operational amplifier and a series of relay controlled scaling resistors of different resistance for detecting circuit feedback; 5) an optional power block section intermediate the power supply and the high voltage DC--DC converter; and 6) a microprocessor receiving feedback information from the feedback network, controlling which of the scaling resistors should be in the circuit and manipulating data from the feedback network to provide accurate vacuum measurement to an operator.

  18. Intense beam production of highly charged heavy ions by the superconducting electron cyclotron resonance ion source SECRAL.

    Science.gov (United States)

    Zhao, H W; Sun, L T; Zhang, X Z; Guo, X H; Cao, Y; Lu, W; Zhang, Z M; Yuan, P; Song, M T; Zhao, H Y; Jin, T; Shang, Y; Zhan, W L; Wei, B W; Xie, D Z

    2008-02-01

    There has been increasing demand to provide higher beam intensity and high enough beam energy for heavy ion accelerator and some other applications, which has driven electron cyclotron resonance (ECR) ion source to produce higher charge state ions with higher beam intensity. One of development trends for highly charged ECR ion source is to build new generation ECR sources by utilization of superconducting magnet technology. SECRAL (superconducting ECR ion source with advanced design in Lanzhou) was successfully built to produce intense beams of highly charged ion for Heavy Ion Research Facility in Lanzhou (HIRFL). The ion source has been optimized to be operated at 28 GHz for its maximum performance. The superconducting magnet confinement configuration of the ion source consists of three axial solenoid coils and six sextupole coils with a cold iron structure as field booster and clamping. An innovative design of SECRAL is that the three axial solenoid coils are located inside of the sextupole bore in order to reduce the interaction forces between the sextupole coils and the solenoid coils. For 28 GHz operation, the magnet assembly can produce peak mirror fields on axis of 3.6 T at injection, 2.2 T at extraction, and a radial sextupole field of 2.0 T at plasma chamber wall. During the commissioning phase at 18 GHz with a stainless steel chamber, tests with various gases and some metals have been conducted with microwave power less than 3.5 kW by two 18 GHz rf generators. It demonstrates the performance is very promising. Some record ion beam intensities have been produced, for instance, 810 e microA of O(7+), 505 e microA of Xe(20+), 306 e microA of Xe(27+), and so on. The effect of the magnetic field configuration on the ion source performance has been studied experimentally. SECRAL has been put into operation to provide highly charged ion beams for HIRFL facility since May 2007.

  19. High Resolution Fluorescence Imaging of Cancers Using Lanthanide Ion-Doped Upconverting Nanocrystals

    Energy Technology Data Exchange (ETDEWEB)

    Naccache, Rafik; Rodríguez, Emma Martín; Bogdan, Nicoleta [Department of Chemistry and Biochemistry, Concordia University, Montreal H4B 1R6 (Canada); Sanz-Rodríguez, Francisco [Departamento de Biología, Facultad de Ciencias, Universidad Autónoma de Madrid, Madrid 28049 (Spain); Cruz, Maria del Carmen Iglesias de la [Departamento de Fisiología. Facultad de Medicina, Universidad Autónoma de Madrid, Madrid 28029 (Spain); Fuente, Ángeles Juarranz de la [Departamento de Biología, Facultad de Ciencias, Universidad Autónoma de Madrid, Madrid 28049 (Spain); Vetrone, Fiorenzo [Institut National de la Recherche Scientifique-Énergie, Matériaux et Télécommunications, Université du Québec, Varennes J3X 1S2 (Canada); Jaque, Daniel; Solé, José García, E-mail: jose.garcia_sole@uam.es [Departamento de Física de Materiales, Universidad Autónoma de Madrid, Madrid 28049 (Spain); Capobianco, John A., E-mail: jose.garcia_sole@uam.es [Department of Chemistry and Biochemistry, Concordia University, Montreal H4B 1R6 (Canada)

    2012-10-22

    During the last decade inorganic luminescent nanoparticles that emit visible light under near infrared (NIR) excitation (in the biological window) have played a relevant role for high resolution imaging of cancer. Indeed, semiconductor quantum dots (QDs) and metal nanoparticles, mostly gold nanorods (GNRs), are already commercially available for this purpose. In this work we review the role which is being played by a relatively new class of nanoparticles, based on lanthanide ion doped nanocrystals, to target and image cancer cells using upconversion fluorescence microscopy. These nanoparticles are insulating nanocrystals that are usually doped with small percentages of two different rare earth (lanthanide) ions: The excited donor ions (usually Yb{sup 3+} ion) that absorb the NIR excitation and the acceptor ions (usually Er{sup 3+}, Ho{sup 3+} or Tm{sup 3+}), that are responsible for the emitted visible (or also near infrared) radiation. The higher conversion efficiency of these nanoparticles in respect to those based on QDs and GNRs, as well as the almost independent excitation/emission properties from the particle size, make them particularly promising for fluorescence imaging. The different approaches of these novel nanoparticles devoted to “in vitro” and “in vivo” cancer imaging, selective targeting and treatment are examined in this review.

  20. High Resolution Fluorescence Imaging of Cancers Using Lanthanide Ion-Doped Upconverting Nanocrystals

    Directory of Open Access Journals (Sweden)

    John A. Capobianco

    2012-10-01

    Full Text Available During the last decade inorganic luminescent nanoparticles that emit visible light under near infrared (NIR excitation (in the biological window have played a relevant role for high resolution imaging of cancer. Indeed, semiconductor quantum dots (QDs and metal nanoparticles, mostly gold nanorods (GNRs, are already commercially available for this purpose. In this work we review the role which is being played by a relatively new class of nanoparticles, based on lanthanide ion doped nanocrystals, to target and image cancer cells using upconversion fluorescence microscopy. These nanoparticles are insulating nanocrystals that are usually doped with small percentages of two different rare earth (lanthanide ions: The excited donor ions (usually Yb3+ ion that absorb the NIR excitation and the acceptor ions (usually Er3+, Ho3+ or Tm3+, that are responsible for the emitted visible (or also near infrared radiation. The higher conversion efficiency of these nanoparticles in respect to those based on QDs and GNRs, as well as the almost independent excitation/emission properties from the particle size, make them particularly promising for fluorescence imaging. The different approaches of these novel nanoparticles devoted to "in vitro" and "in vivo" cancer imaging, selective targeting and treatment are examined in this review.

  1. Apparatus, Method and Program Storage Device for Determining High-Energy Neutron/Ion Transport to a Target of Interest

    Science.gov (United States)

    Wilson, John W. (Inventor); Tripathi, Ram K. (Inventor); Badavi, Francis F. (Inventor); Cucinotta, Francis A. (Inventor)

    2012-01-01

    An apparatus, method and program storage device for determining high-energy neutron/ion transport to a target of interest. Boundaries are defined for calculation of a high-energy neutron/ion transport to a target of interest; the high-energy neutron/ion transport to the target of interest is calculated using numerical procedures selected to reduce local truncation error by including higher order terms and to allow absolute control of propagated error by ensuring truncation error is third order in step size, and using scaling procedures for flux coupling terms modified to improve computed results by adding a scaling factor to terms describing production of j-particles from collisions of k-particles; and the calculated high-energy neutron/ion transport is provided to modeling modules to control an effective radiation dose at the target of interest.

  2. Fluorescent ion-imprinted polymers for selective Cu(II) optosensing.

    Science.gov (United States)

    Pinheiro, Silvia C Lopes; Descalzo, Ana B; Raimundo, Ivo M; Orellana, Guillermo; Moreno-Bondi, María C

    2012-04-01

    This paper describes the synthesis and characterization of a fluorescent ion-imprinted polymer (IIP) for selective determination of copper ions in aqueous samples. The IIP has been prepared using a novel functional monomer, 4-[(E)-2-(4'-methyl-2,2'-bipyridin-4-yl)vinyl]phenyl methacrylate (abbreviated as BSOMe) that has been spectroscopically characterized in methanolic solution, in the absence and in the presence of several metal ions, including Cd(II), Cu(II), Hg(II), Ni(II), Pb(II), and Zn(II). The stability constant (2.04 × 10(8) mol(-2) l(2)) and stoichiometry (L(2)M) of the BSOMe complex with Cu(II) were extracted thereof. Cu(II)-IIPs were prepared by radical polymerization using stoichiometric amounts of the fluorescent monomer and the template metal ion. The resulting cross-linked network did not show any leaching of the immobilized ligand allowing determination of Cu(II) in aqueous samples by fluorescence quenching measurements. Several parameters affecting optosensor performance have been optimized, including sample pH, ionic strength, or polymer regeneration for online analysis of water samples. The synthesized Cu(II)-IIP exhibits a detection limit of 0.04 μmol l(-1) for the determination of Cu(II) in water samples with a reproducibility of 3%, exhibiting an excellent selectivity towards the template ion over other metal ions with the same charge and close ionic radius. The IIP-based optosensor has been repeatedly used and regenerated for more than 50 cycles without a significant decrease in the luminescent properties and binding affinity of the sensing phase.

  3. Rotating disk potentiometry for inner solution optimization of low-detection-limit ion-selective electrodes.

    Science.gov (United States)

    Radu, Aleksandar; Telting-Diaz, Martin; Bakker, Eric

    2003-12-15

    The extent of optimization of the lower detection limit of ion-selective electrodes (ISEs) can be assessed with an elegant new method. At the detection limit (i.e., in the absence of primary ions in the sample), one can observe a reproducible change in the membrane potential upon alteration of the aqueous diffusion layer thickness. This stir effect is predicted to depend on the composition of the inner solution, which is known to influence the lower detection limit of the potentiometric sensor dramatically. For an optimized electrode, the stir effect is calculated to be exactly one-half the value of the case when substantial coextraction occurs at the inner membrane side. In contrast, there is no stir effect when substantial ion exchange occurs at the inner membrane side. Consequently, this experimental method can be used to determine how well the inner filling solution has been optimized. A rotating disk electrode was used in this study because it provides adequate control of the aqueous diffusion layer thickness. Various ion-selective membranes with a variety of inner solutions that gave different calculated concentrations of the complex at the inner membrane side were studied to evaluate this principle. They contained the well-examined silver ionophore O,O' '-bis[2-(methylthio)ethyl]-tert-butylcalix[4]arene, the potassium ionophore valinomycin, or the iodide carrier [9]mercuracarborand-3. Stir effects were determined in different background solutions and compared to theoretical expectations. Correlations were good, and the results encourage the use of such stir-effect measurements to optimize ISE compositions for real-world applications. The technique was also found to be useful in estimating the level of primary ion impurities in the sample. For an iodide-selective electrode measured in phosphoric acid, for example, apparent iodide impurity levels were calculated as 5 x 10(-10) M.

  4. Excitation pathways and efficiency of Eu ions in GaN by site-selective spectroscopy

    Science.gov (United States)

    Fleischman, Z.; Munasinghe, C.; Steckl, A. J.; Wakahara, A.; Zavada, J.; Dierolf, V.

    2009-11-01

    Using combined excitation emission spectroscopy, we performed a comparative study of europium ions in GaN in samples that have been in situ doped during interrupted growth epitaxy (IGE) or conventional molecular beam epitaxy (MBE) as well as samples that were grown using organometallic vapor phase epitaxy (OMVPE) and subsequently ion implanted with Eu ions. Through site-selective resonant excitation, we are able to unambiguously assign all major observed transitions to a combination of different incorporation sites and electron-phonon coupled transitions. We identified at least nine different incorporation sites of Eu ions in GaN and studied how these sites behave under different excitation conditions and how their relative number is modified by different growth and doping conditions. The coupling to phonons has also been studied for a series of Al x Ga1- x N samples with x=0…1. We find that a main site most resembling an unperturbed Eu ion on Ga site is always dominant, while the minority sites are changing substantially in relative numbers and can occur in some samples fairly close in emission intensity to the main site. In terms of the excitation pathway after the creation of electron-hole pairs, we found three types of centers: (1) sites that are dominantly excited through shallow defect traps; (2) sites that are excited through a deep defect trap; (3) sites that cannot be excited at all including the majority of the main sites. We interpret this finding to indicate that the ion in this environment is not very efficient in trapping excitation and that the indirect excitation involving other traps depends on the ion/trap distance. Many of the main sites are far away from these traps and cannot be excited through this channel at all. The efficiency of excitation is highest for the deep traps, indicating that it would be desirable to enrich the respective site, as has been done with some success in the IGE grown samples.

  5. Laboratory and Field Experiments on Expulsion of Selected Ions along Divergent Polar Geomagnetic Fields

    Science.gov (United States)

    Wong, A. Y.; Deng, B.; Quon, B.; Wang, R.; Hartzell, J.; Rosenthal, G.; Hazelton, L. R.

    2007-12-01

    Laboratory and Field Experiments on Expulsion of Selected Ions along Divergent Polar Geomagnetic Fields. Laboratory experiments have shown significant gyro-resonance acceleration of minority ion species in a magnetized plasma. Field aligned elctron drifts can provide free energy needed to make this process efficient. The linear magnetized device has a uniform magnetic field linked to two adjustable mirrors at the ends. Outdoor experiments at HIPAS Facility Ak(1) ( 84 MW ERP ) are used to test this process in the earth's "chimneys" at the two poles. The divergent polar geomagnetic field converts the perpendicular ion velocity into an upward motion. Satellites and ground-based ELF receivers,supplemented by UHF radars, LIDARs and infrared diagnostics , will monitor low-frequency EM waves and upflows of ions. The upward transport of ions in the lower atmosphere by field-induced diffusion and convection and the coupling to the free energy in the auroral region will be discussed. Computer modeling and theoeries complement our experiments. 1. Wong, A.Y. et al. AIP CIP 96-27719, Chap 3, pp 41-75, 1997

  6. Carbazole based nanoprobe for selective recognition of Fe3 + ion in aqueous medium: Spectroscopic insight

    Science.gov (United States)

    Suryawanshi, Sonali B.; Mahajan, Prasad G.; Bodake, Anita J.; Kolekar, Govind B.; Patil, Shivajirao R.

    2017-08-01

    A simple carbazole based nanoprobe prepared by reprecipitation method shows selective sensing behavior for Fe3 + ion in aqueous medium. The prepared SDS capped 9-phenyl carbazole nanoparticles (9-PCzNPs) has narrower particle size distribution with an average diameter 35 nm and zeta potential of - 34.3 mV predicted a good stability with negative surface charge over the nanoparticles. The Field Emission Scanning Electron Microscopy (FE-SEM) image showed cubic shape morphology of nanoparticles. The aqueous suspension of SDS capped 9-phenyl carbazole nanoparticles exhibited aggregation induced enhanced red shifted intense emission in comparison with the emission arising from dilute solution of 9-phenyl carbazole in DCM. The cation recognition test based on fluorescence change shows Fe3 + ion induce significant fluorescence quenching, however remaining cations responds negligibly. The obtained quenching data fit into Stern-Volmer relation in the concentration range of 0.0-1.0 μg·mL- 1 of Fe3 + ion solution and the detection limit is 0.0811 μg·mL- 1. The probable mechanism of fluorescence quenching of SDS capped 9-PCzNPs is because of adsorption of Fe3 + ion over the negatively charged surface of NPs through electrostatic interaction. Thus the proposed method was successfully applied for the detection of Fe3 + ion in environmental water sample.

  7. Characterization of All Solid State Hydrogen Ion Selective Electrode Based on PVC-SR Hybrid Membranes

    Directory of Open Access Journals (Sweden)

    Yoon-Bo Shim

    2003-06-01

    Full Text Available Hydrogen ion selective membranes formulated with 3140 RTV silicone rubber (SR in PVC were studied to extend the life time of solid state ion sensors through improved membrane adhesion. All solid state hydrogen ion selective electrodes were prepared by incorporation of tridodecyl amine (TDDA as an ionophore, potassium tetrakis[3.5-bis(p-chlorophenylborate (KTpClPB as a lipophilic additive, bis(2-ethylhexyladipate (DOA as a plasticizer. Their linear dynamic range was pH 2.0-11.0 and showed the near Nernstian slope of 55.1±0.2 mV/pH (r=0.999. The ifluences from alkali and alkaline earth metal ions were studied for the response of the final ISE membrane composition. Impedance spectroscopic data showed that the resistance was increased by increasing SR content in PVC. Brewster Angle Microscopy (BAM image showed clear differences according to the SR compositions in PVC. Life time of the all solid state membrane electrode was extended to about 2 months by preparing the membrane with PVC and SR. The standard reference material from NIST (2181 HEPES Free acid and 2182 NaHEPESate was tested for the ISE and it gave good result.

  8. Selective Transport of Silver(I Ion Through Polymer Membranes Containing Thioether Donor Macrocycles as Carriers

    Directory of Open Access Journals (Sweden)

    A. Nezhadali

    2008-01-01

    Full Text Available The Preparation of polymer membrane and it's selectivity to silver(I ion from an aqueous solution containing seven metal cations, Co(II, Ni(II, Cu(II, Zn(II, Ag(I, Cd(II and Pb(II, was studied. The source phase contained equimolar concentrations of the above mentioned cations with the source and receiving phases being buffered at pH 5.0 and 3.0 respectively. The effect of variation in the number of the macrocyclic sulfur atom donor set anssd the size of ring 9 and 16 member macrocycles on transport efficiency is presented. Silver(I ion transport occurred (at 25°C from the aqueous source phase across the polymer membrane (derived from cellulos triacetate containing ligands 9-membered, S3-donor and16-membered S4-donor macrocycles as the ionophors in separate experiments into the aqueous receiving phase. Clear transport selectivity for silver(I ion was observed using both thioether donor macrocycles. The efficiency of transport rate for silver(I ion with using 9-membered S3-donor macrocycle as carrier was better than 16-membered S4-donor .

  9. EUV spectral lines of highly-charged Hf, Ta and Au ions observed with an electron beam ion trap

    Energy Technology Data Exchange (ETDEWEB)

    Draganic, Ilija N; Ralchenko, Yuri; Reader, Joseph; Gillaspy, J D; Tan, Joseph N; Pomeroy, Joshua M; Brewer, Samuel M; Osin, Dmitry, E-mail: yuri.ralchenko@nist.gov [National Institute of Standards and Technology, Gaithersburg, MD 20899-8422 (United States)

    2011-01-28

    Extreme ultraviolet spectra of highly-charged hafnium, tantalum and gold were produced with an electron beam ion trap (EBIT) at the National Institute of Standards and Technology (NIST) and recorded with a flat-field grazing-incidence spectrometer in the wavelength range 4-20 nm. The beam energy was varied between 1.84 and 5.15 keV to selectively enhance spectra from specific ionization stages. Identifications of strong n = 4-n = 4 transitions from Rb-like hafnium (35+) to Co-like gold (52+) were determined with the aid of collisional-radiative modelling of the EBIT plasma. Good quantitative agreement between simulated and measured spectra was achieved. Over 150 spectral lines were identified, 115 of which are new.

  10. The high current transport experiment for heavy ion inertial fusion

    Energy Technology Data Exchange (ETDEWEB)

    Prost, L.R.; Baca, D.; Bieniosek, F.M.; Celata, C.M.; Faltens, A.; Henestroza, E.; Kwan, J.W.; Leitner, M.; Seidl, P.A.; Waldron, W.L.; Cohen, R.; Friedman, A.; Grote, D.; Lund, S.M.; Molvik, A.W.; Morse, E.

    2004-05-01

    The High Current Experiment (HCX) at Lawrence Berkeley National Laboratory is part of the US program to explore heavy-ion beam transport at a scale representative of the low-energy end of an induction linac driver for fusion energy production. The primary mission of this experiment is to investigate aperture fill factors acceptable for the transport of space-charge-dominated heavy-ion beams at high intensity (line charge density {approx} 0.2 {micro}C/m) over long pulse durations (4 {micro}s) in alternating gradient focusing lattices of electrostatic or magnetic quadrupoles. This experiment is testing transport issues resulting from nonlinear space-charge effects and collective modes, beam centroid alignment and steering, envelope matching, image charges and focusing field nonlinearities, halo and, electron and gas cloud effects. We present the results for a coasting 1 MeV K{sup +} ion beam transported through ten electrostatic quadrupoles. The measurements cover two different fill factor studies (60% and 80% of the clear aperture radius) for which the transverse phase-space of the beam was characterized in detail, along with beam energy measurements and the first halo measurements. Electrostatic quadrupole transport at high beam fill factor ({approx}80%) is achieved with acceptable emittance growth and beam loss, even though the initial beam distribution is not ideal (but the emittance is low) nor in thermal equilibrium. We achieved good envelope control, and rematching may only be needed every ten lattice periods (at 80% fill factor) in a longer lattice of similar design. We also show that understanding and controlling the time dependence of the envelope parameters is critical to achieving high fill factors, notably because of the injector and matching section dynamics.

  11. High current transport experiment for heavy ion inertial fusion

    Directory of Open Access Journals (Sweden)

    L. R. Prost

    2005-02-01

    Full Text Available The High Current Experiment at Lawrence Berkeley National Laboratory is part of the U.S. program to explore heavy-ion beam transport at a scale representative of the low-energy end of an induction linac driver for fusion energy production. The primary mission of this experiment is to investigate aperture fill factors acceptable for the transport of space-charge-dominated heavy-ion beams at high intensity (line charge density ∼0.2  μC/m over long pulse durations (4  μs in alternating gradient focusing lattices of electrostatic or magnetic quadrupoles. This experiment is testing transport issues resulting from nonlinear space-charge effects and collective modes, beam centroid alignment and steering, envelope matching, image charges and focusing field nonlinearities, halo, and electron and gas cloud effects. We present the results for a coasting 1 MeV K^{+} ion beam transported through ten electrostatic quadrupoles. The measurements cover two different fill factor studies (60% and 80% of the clear aperture radius for which the transverse phase space of the beam was characterized in detail, along with beam energy measurements and the first halo measurements. Electrostatic quadrupole transport at high beam fill factor (≈80% is achieved with acceptable emittance growth and beam loss, even though the initial beam distribution is not ideal (but the emittance is low nor in thermal equilibrium. We achieved good envelope control, and rematching may only be needed every ten lattice periods (at 80% fill factor in a longer lattice of similar design. We also show that understanding and controlling the time dependence of the envelope parameters is critical to achieving high fill factors, notably because of the injector and matching section dynamics.

  12. Ion-selective electrodes with solid contact for heavy metals determination

    Directory of Open Access Journals (Sweden)

    Wardak C.

    2013-04-01

    Full Text Available Potentiometric properties of ion-selective electrodes with solid contact for lead, cadmium and zinc determination were investigated. The ionic liquids (ILs alkyl methyl imidazolium chlorides are used as lipophilic ionic additive to the membrane phase and as transducer media. The basic analytical parameters of the studied electrodes, such as the slope characteristic, the detection limit, response time, lifetime, selectivity coefficients against various inorganic cations as well as the dependence of the electrodes potential on pH were determined. The obtained electrode are characterized by good analytical parameters: theoretical characteristic slope, low detection limit, short response time and very long lifetime. The electrodes was successfully applied to the direct determination of lead, cadmium and zinc ions in waste water samples. The results obtained indicate that the electrodes provide a good alternative for the determination of these heavy metals in real samples.

  13. The measurement of acetanilide in plasma by spectrophotometric and selected ion monitoring methods.

    Science.gov (United States)

    Baty, J D; Playfer, J; Evans, D A; Lamb, J

    1977-08-01

    Plasma samples from volunteers who had received an oral dose of acetanilide have been analysed by gas chromatography mass spectrometry and ultraviolet absorption techniques. The gas chromatography mass spectrometry method involved extraction of the plasma and analysis of the acetanilide using selected ion monitoring with a deuterated internal standard. In the ultraviolet method the plasma was hydrolysed with acid to convert the acetanilide to aniline, and this compound was diazotized and coupled with N-1-naphthylethylene-diamine. The absorbance of the resulting complex was read at 550 nm. Acetanilide levels in plasma determined by the selected ion monitoring method were significantly lower than those measured by spectrophotometry. Pharmacokinetic data calculated from the results obtained using these two assays are very different and illustrate the need for an accurate and specific method of analysis. The major metabolites of acetanilide are shown not to interfere with these assays and the results suggest the possible presence of a new metabolite of acetanilide.

  14. A selectivity filter at the intracellular end of the acid-sensing ion channel pore

    DEFF Research Database (Denmark)

    Lynagh, Timothy; Flood, Emelie; Boiteux, Céline

    2017-01-01

    Increased extracellular proton concentrations during neurotransmission are converted to excitatory sodium influx by acid-sensing ion channels (ASICs). 10-fold sodium/potassium selectivity in ASICs has long been attributed to a central constriction in the channel pore, but experimental verification...... is lacking due to the sensitivity of this structure to conventional manipulations. Here, we explored the basis for ion selectivity by incorporating unnatural amino acids into the channel, engineering channel stoichiometry and performing free energy simulations. We observed no preference for sodium...... at the "GAS belt" in the central constriction. Instead, we identified a band of glutamate and aspartate side chains at the lower end of the pore that enables preferential sodium conduction....

  15. Elasticity and electrical resistivity of chalk and greensand during water flooding with selective ions

    DEFF Research Database (Denmark)

    Katika, Konstantina; Alam, Mohammad Monzurul; Alexeev, Artem

    2018-01-01

    Water flooding with selective ions has in some cases lead to increased oil recovery. We investigate the physical processes on a pore scale that are responsible for changes in petrophysical and mechanical properties of four oil-bearing chalk and four oil-bearing greensand samples caused by flooding...... with brines containing varying amounts of dissolved NaCl, Na2SO4, MgCl2 and MgSO4. Ultrasonic P-wave velocity and AC resistivity measurements were performed prior to, during and after flow through experiments in order to identify and quantify the processes related to water flooding with selective ions. Low...... field Nuclear Magnetic Resonance (NMR) spectrometry measurements were performed at full water saturation, at irreducible water saturation, after aging and after flooding. CT-scanning, X-ray diffraction (XRD), backscatter electron microscopy images (BSEM), mercury injection capillary pressure (MICP...

  16. Recent U.S. advances in ion-beam-driven high energy densityphysics and heavy ion fusion

    Energy Technology Data Exchange (ETDEWEB)

    Logan, B.G.; Bieniosek, F.M.; Celata, C.M.; Coleman, J.; Greenway, W.; Henestroza, E.; Kwan, J.W.; Lee, E.P.; Leitner, M.; Roy,P.K.; Seidl, P.A.; Vay, J-L.; Waldron, W.L.; Yu, S.S.; Barnard, J.J.; Cohen, R.H.; Friedman, A.; Grote, D.P.; Kireeff Covo, M.; Molvik, A.W.; Lund, S.M.; Meier, W.R.; Sharp, W.; Davidson, R.C.; Efthimion, P.C.; Gilson, E.P.; Grisham, L.; Kaganovich, Qin H.; Sefkow, A.B.; Startsev,E.A.; Welch, D.; Olson, C.

    2006-07-05

    During the past two years, significant experimental and theoretical progress has been made in the US heavy ion fusion science program in longitudinal beam compression, ion-beam-driven warm dense matter, beam acceleration, high brightness beam transport; and advanced theory and numerical simulations. Innovations in longitudinal compression of intense ion beams by > 50 X propagating through background plasma enable initial beam target experiments in warm dense matter to begin within the next two years. They are assessing how these new techniques might apply to heavy ion fusion drivers for inertial fusion energy.

  17. Analytical possibilities of highly focused ion beams in biomedical field

    Science.gov (United States)

    Ren, M. Q.; Ji, X.; Vajandar, S. K.; Mi, Z. H.; Hoi, A.; Walczyk, T.; van Kan, J. A.; Bettiol, A. A.; Watt, F.; Osipowicz, T.

    2017-09-01

    At the Centre for Ion Beam Applications (CIBA), a 3.5 MV HVEE Singletron™ accelerator serves to provide MeV ion beams (mostly protons or He+) to six state-of-the-art beam lines, four of which are equipped with Oxford triplet magnetic quadrupole lens systems. This facility is used for a wide range of research projects, many of which are in the field of biomedicine. Here we presented a discussion of currently ongoing biomedical work carried out using two beamlines: The Nuclear Microscopy (NM) beamline is mainly used for trace elemental quantitative mapping using a combination of Particle Induced X-ray Emission (PIXE), to measure the trace elemental concentration of inorganic elements, Rutherford Backscattering Spectrometry (RBS), to characterise the organic matrix, and Scanning Transmission Ion Microscopy (STIM) to provide information on the lateral areal density variations of the specimen. Typically, a 2.1 MeV proton beam, focused to 1-2 μm spot size with a current of 100 pA is used. The high resolution single cell imaging beamline is equipped with direct STIM to image the interior structure of single cells with proton and alpha particles of sub-50 nm beam spot sizes. Simultaneously, forward scattering transmission ion microscopy (FSTIM) is utilized to generate images with improved contrast of nanoparticles with higher atomic numbers, such as gold nanoparticles, and fluorescent nanoparticles can be imaged using Proton Induced Fluorescence (PIF). Lastly, in this facility, RBS has been included as an option if required to determine the depth distribution of nanoparticles in cells, albeit with reduced spatial resolution.

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

    Science.gov (United States)

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

    2016-11-21

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

  19. Highly porous carbon with large electrochemical ion absorption capability for high-performance supercapacitors and ion capacitors

    Science.gov (United States)

    Wang, Shijie; Wang, Rutao; Zhang, Yabin; Zhang, Li

    2017-11-01

    Carbon-based supercapacitors have attracted extensive attention as the complement to batteries, owing to their durable lifespan and superiority in high-power-demand fields. However, their widespread use is limited by the low energy storage density; thus, a high-surface-area porous carbon is urgently needed. Herein, a highly porous carbon with a Brunauer-Emmett-Teller specific surface area up to 3643 m2 g-1 has been synthesized by chemical activation of papayas for the first time. This sp2-bonded porous carbon has a continuous three-dimensional network of highly curved, atom-thick walls that form narrow mesopores of 2 ˜ 5 nm in width, which can be systematically tailored with varied activation levels. Two-electrode symmetric supercapacitors constructed by this porous carbon achieve energy density of 8.1 Wh kg-1 in aqueous electrolyte and 65.5 Wh kg-1 in ionic-liquid electrolyte. Furthermore, half-cells (versus Li or Na metal) using this porous carbon as ion sorption cathodes yield high specific capacity, e.g., 51.0 and 39.3 mAh g-1 in Li+ and Na+ based organic electrolyte. These results underline the possibility of obtaining the porous carbon for high-performance carbon-based supercapacitors and ion capacitors in a readily scalable and economical way.

  20. Ion-selective detection by plasticized poly(vinyl chloride) membrane in glass nanopipette with alternating voltage modulation.

    Science.gov (United States)

    Deng, Xiao Long; Takami, Tomohide; Son, Jong Wan; Kang, Eun Ji; Kawai, Tomoji; Park, Bae Ho

    2013-08-01

    An alternating current (AC) voltage modulation was applied to ion-selective observations with plasticized poly(vinyl chloride) membranes in glass nanopipettes. The liquid confronting the membranes in the nanopipettes, the conditioning process, and AC voltage modulation play important roles in the ion-selective detection. In the AC detection system developed by us, where distilled water was used as the liquid within the nanopipettes, potassium ions were selectively detected in the sample solution of sodium and potassium ions because sodium ions were captured at the membrane containing bis(12-crown-4) ionophores, before the saturation of the ionophores. The membrane lost the selectivity after the saturation. On using sodium chloride as the liquid within the nanopipette, the membrane selectively detected potassium and sodium ions before and after the saturation of ionophores, respectively. The ion-selective detection of our system can be explained by the ion extraction-diffusion-dissolution mechanism through the bis(12-crown-4) ionophores with AC voltage modulation.

  1. High $p_{T}$ physics in the heavy ion era

    CERN Document Server

    Rak, Jan

    2013-01-01

    Aimed at graduate students and researchers in the field of high-energy nuclear physics, this book provides an overview of the basic concepts of large transverse momentum particle physics, with a focus on pQCD phenomena. It examines high $p_{T}$ probes of relativistic heavy-ion collisions and will serve as a handbook for those working on RHIC and LHC data analyses. Starting with an introduction and review of the field, the authors look at basic observables and experimental techniques, concentrating on relativistic particle kinematics, before moving onto a discussion about the origins of high $p_{T}$ physics. The main features of high $p_{T}$ physics are placed within a historical context and the authors adopt an experimental outlook, highlighting the most important discoveries leading up to the foundation of modern QCD theory. Advanced methods are described in detail, making this book especially useful for newcomers to the field.

  2. Preparation of 3D nanoporous copper-supported cuprous oxide for high-performance lithium ion battery anodes.

    Science.gov (United States)

    Liu, Dequan; Yang, Zhibo; Wang, Peng; Li, Fei; Wang, Desheng; He, Deyan

    2013-03-07

    Three-dimensional (3D) nanoporous architectures can provide efficient and rapid pathways for Li-ion and electron transport as well as short solid-state diffusion lengths in lithium ion batteries (LIBs). In this work, 3D nanoporous copper-supported cuprous oxide was successfully fabricated by low-cost selective etching of an electron-beam melted Cu(50)Al(50) alloy and subsequent in situ thermal oxidation. The architecture was used as an anode in lithium ion batteries. In the first cycle, the sample delivered an extremely high lithium storage capacity of about 2.35 mA h cm(-2). A high reversible capacity of 1.45 mA h cm(-2) was achieved after 120 cycles. This work develops a promising approach to building reliable 3D nanostructured electrodes for high-performance lithium ion batteries.

  3. Selective filling of photonic crystal fibers using focused ion beam milled microchannels

    DEFF Research Database (Denmark)

    Wang, Fei; Yuan, Scott Wu; Hansen, Ole

    2011-01-01

    We introduce a versatile, robust, and integrated technique to selectively fill fluid into a desired pattern of air holes in a photonic crystal fiber (PCF). Focused ion beam (FIB) is used to efficiently mill a microchannel on the end facet of a PCF before it is spliced to a single-mode fiber (SMF......). Selected air holes are therefore exposed to the atmosphere through the microchannel for fluid filling. A low-loss in-line tunable optical hybrid fiber device is demonstrated by using such a technique. (C) 2011 Optical Society of America...

  4. Highly sensitive urea sensing with ion-irradiated polymer foils

    Energy Technology Data Exchange (ETDEWEB)

    Fink, Dietmar, E-mail: fink@daad-alumni.de [Departamento de Fisica, Universidad Autonoma Metropolitana-Iztapalapa, P.O. Box 55-534, 09340 Mexico, D.F. (Mexico); Nuclear Physics Institute, Academy of Sciences of the Czech Republic, 250 68 Rez (Czech Republic); Munoz Hernandez, Gerardo [Departamento de Fisica, Universidad Autonoma Metropolitana-Iztapalapa, P.O. Box 55-534, 09340 Mexico, D.F. (Mexico); Division de Ciencias Naturales e Ingenieria, Universidad Autonoma Metropolitana-Cuajimalpa, Pedro Antonio de los Santos 84, Col. Sn. Miguel Chapultepec, C.P. 11850, Mexico, D.F. (Mexico); Alfonta, Lital, E-mail: alfontal@bgu.ac.il [Avram and Stella Goldstein-Goren Department of Biotechnology Engineering, Ben-Gurion University of the Negev, P.O. Box 653, Beer-Sheva 84105 (Israel)

    2012-02-15

    Recently we prepared urea-sensors by attaching urease to the inner walls of etched ion tracks within thin polymer foil. Here, alternative track-based sensor configurations are examined where the enzyme remained in solution. The conductivities of systems consisting of two parallel irradiated polymer foils and confining different urea/urease mixtures in between were examined. The correlations between conductivity and urea concentration differed strongly for foils with unetched and etched tracks, which points at different sensing mechanisms - tentatively attributed to the adsorption of enzymatic reaction products on the latent track entrances and to the enhanced conductivity of reaction product-filled etched tracks, respectively. All examined systems enable in principle, urea sensing. They point at the possibility of sensor cascade construction for more sensitive or selective sensor systems.

  5. O+ and H+ ion heat fluxes at high altitudes and high latitudes

    Directory of Open Access Journals (Sweden)

    I. A. Barghouthi

    2014-08-01

    Full Text Available Higher order moments, e.g., perpendicular and parallel heat fluxes, are related to non-Maxwellian plasma distributions. Such distributions are common when the plasma environment is not collision dominated. In the polar wind and auroral regions, the ion outflow is collisionless at altitudes above about 1.2 RE geocentric. In these regions wave–particle interaction is the primary acceleration mechanism of outflowing ionospheric origin ions. We present the altitude profiles of actual and "thermalized" heat fluxes for major ion species in the collisionless region by using the Barghouthi model. By comparing the actual and "thermalized" heat fluxes, we can see whether the heat flux corresponds to a small perturbation of an approximately bi-Maxwellian distribution (actual heat flux is small compared to "thermalized" heat flux, or whether it represents a significant deviation (actual heat flux equal or larger than "thermalized" heat flux. The model takes into account ion heating due to wave–particle interactions as well as the effects of gravity, ambipolar electric field, and divergence of geomagnetic field lines. In the discussion of the ion heat fluxes, we find that (1 the role of the ions located in the energetic tail of the ion velocity distribution function is very significant and has to be taken into consideration when modeling the ion heat flux at high altitudes and high latitudes; (2 at times the parallel and perpendicular heat fluxes have different signs at the same altitude. This indicates that the parallel and perpendicular parts of the ion energy are being transported in opposite directions. This behavior is the result of many competing processes; (3 we identify altitude regions where the actual heat flux is small as compared to the "thermalized" heat flux. In such regions we expect transport equation solutions based on perturbations of bi-Maxwellian distributions to be applicable. This is true for large altitude intervals for protons

  6. Ion energy characteristics downstream of a high power helicon

    Energy Technology Data Exchange (ETDEWEB)

    Prager, James; Winglee, Robert; Ziemba, Tim; Roberson, B Race; Quetin, Gregory [University of Washington, Johnson Hall 070, Box 351310, 4000 15th Avenue NE, Seattle, WA 98195-1310 (United States)], E-mail: jprager@u.washington.edu

    2008-05-01

    The High Power Helicon eXperiment operates at higher powers (37 kW) and lower background neutral pressure than other helicon experiments. The ion velocity distribution function (IVDF) has been measured at multiple locations downstream of the helicon source and a mach 3-6 flowing plasma was observed. The helicon antenna has a direct effect in accelerating the plasma downstream of the source. Also, the IVDF is affected by the cloud of neutrals from the initial gas puff, which keeps the plasma speed low at early times near the source.

  7. Precision, high dose radiotherapy: helium ion treatment of uveal melanoma

    Energy Technology Data Exchange (ETDEWEB)

    Saunders, W.M.; Char, D.H.; Quivey, J.M.; Castro, J.R.; Chen, G.T.Y.; Collier, J.M.; Cartigny, A.; Blakely, E.A.; Lyman, J.T.; Zink, S.R.

    1985-02-01

    The authors report on 75 patients with uveal melanoma who were treated by placing the Bragg peak of a helium ion beam over the tumor volume. The technique localizes the high dose region very tightly around the tumor volume. This allows critical structures, such as the optic disc and the macula, to be excluded from the high dose region as long as they are 3 to 4 mm away from the edge of the tumor. Careful attention to tumor localization, treatment planning, patient immobilization and treatment verification is required. With a mean follow-up of 22 months (3 to 60 months) the authors have had only five patients with a local recurrence, all of whom were salvaged with another treatment. Pretreatment visual acuity has generally been preserved as long as the tumor edge is at least 4 mm away from the macula and optic disc. The only serious complication to date has been an 18% incidence of neovascular glaucoma in the patients treated at our highest dose level. Clinical results and details of the technique are presented to illustrate potential clinical precision in administering high dose radiotherapy with charged particles such as helium ions or protons.

  8. Dissociation of internal energy-selected methyl bromide ion revealed from threshold photoelectron-photoion coincidence velocity imaging

    Energy Technology Data Exchange (ETDEWEB)

    Tang, Xiaofeng [Hefei National Laboratory for Physical Sciences at the Microscale and Department of Chemical Physics, University of Science and Technology of China, Hefei 230026 (China); National Synchrotron Radiation Laboratory, University of Science and Technology of China, Hefei 230029 (China); Zhou, Xiaoguo, E-mail: xzhou@ustc.edu.cn, E-mail: yanbing@jlu.edu.cn; Liu, Shilin [Hefei National Laboratory for Physical Sciences at the Microscale and Department of Chemical Physics, University of Science and Technology of China, Hefei 230026 (China); Synergetic Innovation Center of Quantum Information and Quantum Physics, University of Science and Technology of China, Hefei, Anhui 230026 (China); Sun, Zhongfa [Hefei National Laboratory for Physical Sciences at the Microscale and Department of Chemical Physics, University of Science and Technology of China, Hefei 230026 (China); Liu, Fuyi; Sheng, Liusi [National Synchrotron Radiation Laboratory, University of Science and Technology of China, Hefei 230029 (China); Yan, Bing, E-mail: xzhou@ustc.edu.cn, E-mail: yanbing@jlu.edu.cn [Institute of Atomic and Molecular Physics, Jilin University, Changchun 130012 (China)

    2014-01-28

    Dissociative photoionization of methyl bromide (CH{sub 3}Br) in an excitation energy range of 10.45–16.90 eV has been investigated by using threshold photoelectron-photoion coincidence (TPEPICO) velocity imaging. The coincident time-of-flight mass spectra indicate that the ground state X{sup 2}E of CH{sub 3}Br{sup +} is stable, and both A{sup 2}A{sub 1} and B{sup 2}E ionic excited states are fully dissociative to produce the unique fragment ion of CH{sub 3}{sup +}. From TPEPICO 3D time-sliced velocity images of CH{sub 3}{sup +} dissociated from specific state-selected CH{sub 3}Br{sup +} ion, kinetic energy release distribution (KERD) and angular distribution of CH{sub 3}{sup +} fragment ion are directly obtained. Both spin-orbit states of Br({sup 2}P) atom can be clearly observed in fast dissociation of CH{sub 3}Br{sup +}(A{sup 2}A{sub 1}) ion along C–Br rupture, while a KERD of Maxwell-Boltzmann profile is obtained in dissociation of CH{sub 3}Br{sup +}(B{sup 2}E) ion. With the aid of the re-calculated potential energy curves of CH{sub 3}Br{sup +} including spin-orbit coupling, dissociation mechanisms of CH{sub 3}Br{sup +} ion in A{sup 2}A{sub 1} and B{sup 2}E states along C–Br rupture are revealed. For CH{sub 3}Br{sup +}(A{sup 2}A{sub 1}) ion, the CH{sub 3}{sup +} + Br({sup 2}P{sub 1/2}) channel is occurred via an adiabatic dissociation by vibration, while the Br({sup 2}P{sub 3/2}) formation is through vibronic coupling to the high vibrational level of X{sup 2}E state followed by rapid dissociation. C–Br bond breaking of CH{sub 3}Br{sup +}(B{sup 2}E) ion can occur via slow internal conversion to the excited vibrational level of the lower electronic states and then dissociation.

  9. C-H functionalization: thoroughly tuning ligands at a metal ion, a chemist can greatly enhance catalyst's activity and selectivity.

    Science.gov (United States)

    Shul'pin, Georgiy B

    2013-09-28

    This brief essay consists of a few "exciting stories" devoted to relations within a metal-complex catalyst between a metal ion and a coordinated ligand. When, as in the case of a human couple, the rapport of the partners is cordial and a love cements these relations, a chemist finds an ideal married couple, in other words he obtains a catalyst of choice which allows him to functionalize C-H bonds very efficiently and selectively. Examples of such lucky marriages in the catalytic world of ions and ligands are discussed here. Activity of the catalyst is characterized by turnover number (TON) or turnover frequency (TOF) as well as by yield of a target product. Introducing a chelating N,N- or N,O-ligand to the catalyst molecule (this can be an iron or manganese derivative) sharply enhances its activity. However, the activity of vanadium derivatives (with additionally added to the solution pyrazinecarboxylic acid, PCA) as well as of various osmium complexes does not dramatically depend on the nature of ligands surrounding metal ions. Complexes of these metals are very efficient catalysts in oxidations with H2O2. Osmium derivatives are record-holders exhibiting extremely high TONs whereas vanadium complexes are on the second position. Finally, elegant examples of alkane functionalization on the ions of non-transition metals (aluminium, gallium etc.) are described when one ligand within the metal complex (namely, hydroperoxyl ligand HOO(-)) helps other ligand of this complex (H2O2 molecule coordinated to the metal) to disintegrate into two species, generating very reactive hydroxyl radical. Hydrogen peroxide molecule, even ligated to the metal ion, is perfectly stable without the assistance of the neighboring HOO(-) ligand. This ligand can be easily oxidized donating an electron to its partner ligand (H2O2). In an analogous case, when the central ion in the catalyst is a transition metal, this ion changing its oxidation state can donate an electron to the coordinated H2O2

  10. H- Ion Sources for High Intensity Proton Drivers

    Energy Technology Data Exchange (ETDEWEB)

    Johnson, Rolland Paul [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Dudnikov, Vadim [Muons, Inc., Batavia, IL (United States)

    2015-02-20

    Existing RF Surface Plasma Sources (SPS) for accelerators have specific efficiencies for H+ and H- ion generation around 3 to 5 mA/cm2 per kW, where about 50 kW of RF power is typically needed for 50 mA beam current production. The Saddle Antenna (SA) SPS described here was developed to improve H- ion production efficiency, reliability and availability for pulsed operation as used in the ORNL Spallation Neutron Source . At low RF power, the efficiency of positive ion generation in the plasma has been improved to 200 mA/cm2 per kW of RF power at 13.56 MHz. Initial cesiation of the SPS was performed by heating cesium chromate cartridges by discharge as was done in the very first versions of the SPS. A small oven to decompose cesium compounds and alloys was developed and tested. After cesiation, the current of negative ions to the collector was increased from 1 mA to 10 mA with RF power 1.5 kW in the plasma (6 mm diameter emission aperture) and up to 30 mA with 4 kW RF power in the plasma and 250 Gauss longitudinal magnetic field. The ratio of electron current to negative ion current was improved from 30 to 2. Stable generation of H- beam without intensity degradation was demonstrated in the aluminum nitride (AlN) discharge chamber for 32 days at high discharge power in an RF SPS with an external antenna. Some modifications were made to improve the cooling and cesiation stability. The extracted collector current can be increased significantly by optimizing the longitudinal magnetic field in the discharge chamber. While this project demonstrated the advantages of the pulsed version of the SA RF SPS as an upgrade to the ORNL Spallation Neutron Source, it led to a possibility for upgrades to CW machines like the many cyclotrons used for commercial applications. Four appendices contain important details of the work carried out under this grant.

  11. Correlation of precursor and product ions in single-stage high resolution mass spectrometry. A tool for detecting diagnostic ions and improving the precursor elemental composition elucidation

    Energy Technology Data Exchange (ETDEWEB)

    Borràs, S. [Departament de Química Analítica, Universitat de Barcelona, Martí i Franquès 1-11, 08028 Barcelona (Spain); Kaufmann, A., E-mail: anton.kaufmann@klzh.ch [Official Food Control Authority, Fehrenstrasse 15, 8032 Zürich (Switzerland); Companyó, R. [Departament de Química Analítica, Universitat de Barcelona, Martí i Franquès 1-11, 08028 Barcelona (Spain)

    2013-04-15

    Highlights: ► We are describing a technique to spot ions which are derived from each other. ► Single stage high resolution data is used. ► This “in silicon” technique is compared to conventional precursor scan. ► Some applications for this technique are presented. -- Abstract: Monitoring of common diagnostic fragments is essential for recognizing molecules which are members of a particular compound class. Up to now, unit resolving tandem quadrupole mass spectrometers, operating in the precursor ion scan mode, have been typically used to perform such analysis. By means of high-resolution mass spectrometry (HRMS) a much more sensitive and selective detection can be achieved. However, using a single-stage HRMS instrument, there is no unequivocal link to the corresponding precursor ion, since such instrumentation does not permit a previous precursor selection. Thus, to address this limitation, an in silico approach to locate precursor ions, based on diagnostic fragments, was developed. Implemented as an Excel macro, the algorithm rapidly assembles and surveys exact mass data to provide a list of feasible precursor candidates according to the correlation of the chromatographic peak shape profile and other additional filtering criteria (e.g. neutral losses and isotopes). The macro was tested with two families of veterinary drugs, sulfonamides and penicillins, which are known to yield diagnostic product ions when fragmented. Data sets obtained from different food matrices (fish and liver), both at high and low concentration of the target compounds, were investigated in order to evaluate the capabilities and limitations of the reported approach. Finally, other possible applications of this technique, such as the elucidation of elemental compositions based on product ions and corresponding neutral losses, were also presented and discussed.

  12. Development of a High-Throughput Ion-Exchange Resin Characterization Workflow.

    Science.gov (United States)

    Liu, Chun; Dermody, Daniel; Harris, Keith; Boomgaard, Thomas; Sweeney, Jeff; Gisch, Daryl; Goltz, Bob

    2017-06-12

    A novel high-throughout (HTR) ion-exchange (IEX) resin workflow has been developed for characterizing ion exchange equilibrium of commercial and experimental IEX resins against a range of different applications where water environment differs from site to site. Because of its much higher throughput, design of experiment (DOE) methodology can be easily applied for studying the effects of multiple factors on resin performance. Two case studies will be presented to illustrate the efficacy of the combined HTR workflow and DOE method. In case study one, a series of anion exchange resins have been screened for selective removal of NO3- and NO2- in water environments consisting of multiple other anions, varied pH, and ionic strength. The response surface model (RSM) is developed to statistically correlate the resin performance with the water composition and predict the best resin candidate. In case study two, the same HTR workflow and DOE method have been applied for screening different cation exchange resins in terms of the selective removal of Mg2+, Ca2+, and Ba2+ from high total dissolved salt (TDS) water. A master DOE model including all of the cation exchange resins is created to predict divalent cation removal by different IEX resins under specific conditions, from which the best resin candidates can be identified. The successful adoption of HTR workflow and DOE method for studying the ion exchange of IEX resins can significantly reduce the resources and time to address industry and application needs.

  13. High Resolution Helium Ion Scanning Microscopy of the Rat Kidney

    Science.gov (United States)

    Rice, William L.; Van Hoek, Alfred N.; Păunescu, Teodor G.; Huynh, Chuong; Goetze, Bernhard; Singh, Bipin; Scipioni, Larry; Stern, Lewis A.; Brown, Dennis

    2013-01-01

    Helium ion scanning microscopy is a novel imaging technology with the potential to provide sub-nanometer resolution images of uncoated biological tissues. So far, however, it has been used mainly in materials science applications. Here, we took advantage of helium ion microscopy to explore the epithelium of the rat kidney with unsurpassed image quality and detail. In addition, we evaluated different tissue preparation methods for their ability to preserve tissue architecture. We found that high contrast, high resolution imaging of the renal tubule surface is possible with a relatively simple processing procedure that consists of transcardial perfusion with aldehyde fixatives, vibratome tissue sectioning, tissue dehydration with graded methanol solutions and careful critical point drying. Coupled with the helium ion system, fine details such as membrane texture and membranous nanoprojections on the glomerular podocytes were visualized, and pores within the filtration slit diaphragm could be seen in much greater detail than in previous scanning EM studies. In the collecting duct, the extensive and striking apical microplicae of the intercalated cells were imaged without the shrunken or distorted appearance that is typical with conventional sample processing and scanning electron microscopy. Membrane depressions visible on principal cells suggest possible endo- or exocytotic events, and central cilia on these cells were imaged with remarkable preservation and clarity. We also demonstrate the use of colloidal gold probes for highlighting specific cell-surface proteins and find that 15 nm gold labels are practical and easily distinguishable, indicating that external labels of various sizes can be used to detect multiple targets in the same tissue. We conclude that this technology represents a technical breakthrough in imaging the topographical ultrastructure of animal tissues. Its use in future studies should allow the study of fine cellular details and provide

  14. High resolution helium ion scanning microscopy of the rat kidney.

    Science.gov (United States)

    Rice, William L; Van Hoek, Alfred N; Păunescu, Teodor G; Huynh, Chuong; Goetze, Bernhard; Singh, Bipin; Scipioni, Larry; Stern, Lewis A; Brown, Dennis

    2013-01-01

    Helium ion scanning microscopy is a novel imaging technology with the potential to provide sub-nanometer resolution images of uncoated biological tissues. So far, however, it has been used mainly in materials science applications. Here, we took advantage of helium ion microscopy to explore the epithelium of the rat kidney with unsurpassed image quality and detail. In addition, we evaluated different tissue preparation methods for their ability to preserve tissue architecture. We found that high contrast, high resolution imaging of the renal tubule surface is possible with a relatively simple processing procedure that consists of transcardial perfusion with aldehyde fixatives, vibratome tissue sectioning, tissue dehydration with graded methanol solutions and careful critical point drying. Coupled with the helium ion system, fine details such as membrane texture and membranous nanoprojections on the glomerular podocytes were visualized, and pores within the filtration slit diaphragm could be seen in much greater detail than in previous scanning EM studies. In the collecting duct, the extensive and striking apical microplicae of the intercalated cells were imaged without the shrunken or distorted appearance that is typical with conventional sample processing and scanning electron microscopy. Membrane depressions visible on principal cells suggest possible endo- or exocytotic events, and central cilia on these cells were imaged with remarkable preservation and clarity. We also demonstrate the use of colloidal gold probes for highlighting specific cell-surface proteins and find that 15 nm gold labels are practical and easily distinguishable, indicating that external labels of various sizes can be used to detect multiple targets in the same tissue. We conclude that this technology represents a technical breakthrough in imaging the topographical ultrastructure of animal tissues. Its use in future studies should allow the study of fine cellular details and provide

  15. High resolution helium ion scanning microscopy of the rat kidney.

    Directory of Open Access Journals (Sweden)

    William L Rice

    Full Text Available Helium ion scanning microscopy is a novel imaging technology with the potential to provide sub-nanometer resolution images of uncoated biological tissues. So far, however, it has been used mainly in materials science applications. Here, we took advantage of helium ion microscopy to explore the epithelium of the rat kidney with unsurpassed image quality and detail. In addition, we evaluated different tissue preparation methods for their ability to preserve tissue architecture. We found that high contrast, high resolution imaging of the renal tubule surface is possible with a relatively simple processing procedure that consists of transcardial perfusion with aldehyde fixatives, vibratome tissue sectioning, tissue dehydration with graded methanol solutions and careful critical point drying. Coupled with the helium ion system, fine details such as membrane texture and membranous nanoprojections on the glomerular podocytes were visualized, and pores within the filtration slit diaphragm could be seen in much greater detail than in previous scanning EM studies. In the collecting duct, the extensive and striking apical microplicae of the intercalated cells were imaged without the shrunken or distorted appearance that is typical with conventional sample processing and scanning electron microscopy. Membrane depressions visible on principal cells suggest possible endo- or exocytotic events, and central cilia on these cells were imaged with remarkable preservation and clarity. We also demonstrate the use of colloidal gold probes for highlighting specific cell-surface proteins and find that 15 nm gold labels are practical and easily distinguishable, indicating that external labels of various sizes can be used to detect multiple targets in the same tissue. We conclude that this technology represents a technical breakthrough in imaging the topographical ultrastructure of animal tissues. Its use in future studies should allow the study of fine cellular details

  16. Achieving High Resolution Ion Mobility Separations Using Traveling Waves in Compact Multiturn Structures for Lossless Ion Manipulations

    Energy Technology Data Exchange (ETDEWEB)

    Hamid, Ahmed M.; Garimella, Sandilya V. B.; Ibrahim, Yehia M.; Deng, Liulin; Zheng, Xueyun; Webb, Ian K.; Anderson, Gordon A.; Prost, Spencer A.; Norheim, Randolph V.; Tolmachev, Aleksey V.; Baker, Erin S.; Smith, Richard D.

    2016-09-20

    We report on ion mobility separations (IMS) achievable using traveling waves in a Structures for Lossless Ion Manipulations (TW-SLIM) module having a 44-cm path length and sixteen 90º turns. The performance of the TW-SLIM module was evaluated for ion transmission, and ion mobility separations with different RF, TW parameters and SLIM surface gaps in conjunction with mass spectrometry. In this work TWs were created by the transient and dynamic application of DC potentials. The TW-SLIM module demonstrated highly robust performance and the ion mobility resolution achieved even with sixteen close spaced turns was comparable to a similar straight path TW-SLIM module. We found an ion mobility peak capacity of ~ 31 and peak generation rate of 780 s-1 for TW speeds of <210 m/s using the current multi-turn TW-SLIM module. The separations achieved for isomers of peptides and tetrasaccharides were found to be comparable to those from a ~ 0.9-m drift tube-based IMS-MS platform operated at the same pressure (4 torr). The combined attributes of flexible design, low voltage requirements and lossless ion transmission through multiple turns for the present TW-SLIM module provides a basis for SLIM devices capable of achieving much greater ion mobility resolutions via greatly extended ion path lengths and compact serpentine designs that do not significantly impact the instrumentation profile, a direction described in a companion manuscript.

  17. Functionalized graphene for high performance lithium ion capacitors.

    Science.gov (United States)

    Lee, Ji Hoon; Shin, Weon Ho; Ryou, Myung-Hyun; Jin, Jae Kyu; Kim, Junhyung; Choi, Jang Wook

    2012-12-01

    Lithium ion capacitors (LICs) have recently drawn considerable attention because they utilize the advantages of supercapacitors (high power) and lithium ion batteries (high energy). However, the energy densities of conventional LICs, which consist of a pair of graphite and activated carbon electrodes, are limited by the small capacities of the activated carbon cathodes. To overcome this limitation, we have engaged urea-reduced graphene oxide. The amide functional groups generated during the urea reduction facilitate the enolization processes for reversible Li binding, which improves the specific capacity by 37 % compared to those of conventional systems such as activated carbon and hydrazine-reduced graphene oxide. Utilizing the increased Li binding capability, when evaluated based on the mass of the active materials on both sides, the LICs based on urea-reduced graphene oxide deliver a specific energy density of approximately 106 Wh kg(total) (-1) and a specific power density of approximately 4200 W kg(total) (-1) with perfect capacity retention up to 1000 cycles. These values are far superior to those of previously reported LICs and supercapacitors, which suggests that appropriately treated graphene can be a promising electrode material for LICs. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  18. Highly selective second order derivative spectrophotometry for ...

    African Journals Online (AJOL)

    The zero crossing point at 369.8 nm for nickel and the amplitude measurement at 410 nm for cobalt were employed in the simultaneous determinations. A large number of foreign ions do not interfere in the present method. The present simultaneous method is used for the determination of micro amounts of nickel and cobalt ...

  19. Selective calcium ion detection with functionalized ZnO nanorods-extended gate MOSFET.

    Science.gov (United States)

    Asif, M H; Nur, O; Willander, M; Danielsson, B

    2009-07-15

    Zinc oxide nanorod-extended gate field effect transistor (MOSFET) is demonstrated for the detection of calcium (Ca(2+)) ions. ZnO nanorods were grown on the surface of a silver wire to produce an electrochemical nanosensor for selectively detecting Ca(2+). The electrochemical response from the interaction between the ZnO nanorods and Ca(2+) in an aqueous solution is coupled directly to the gate of a field effect transistor (MOSFET). The induced voltage change on the gate results in a measureable current response. In order to adapt the sensors for Ca(2+) ions measurements in biological fluids with sufficient selectivity and stability, a plastic membrane coating containing ionophores was applied on the nanorods. The sensor exhibited a linear response within the range of interest from 1 microM to 1 mM. This work demonstrates a simple technique for sensitive detection of Ca(2+) ions by efficient transfer of the chemical response directly to a standard electronic component producing a low impedance signal.

  20. Selection and impedance based model of a lithium ion battery technology for integration with virtual power plant

    DEFF Research Database (Denmark)

    Swierczynski, Maciej Jozef; Stroe, Daniel Ioan; Stan, Ana-Irina

    2013-01-01

    is to integrate lithium-ion batteries into virtual power plants; thus, the power system stability and the energy quality can be increased. The selection of the best lithium-ion battery candidate for integration with wind power plants is a key aspect for the economic feasibility of the virtual power plant...... investment. This paper presents a methodology for selection, between three candidates, of a Li-ion battery which offers long cycle lifetime at partial charge/discharge (required by many grid support applications) while providing a low cost per cycle also. For the selected Li-ion battery an impedance......-based diagnostic tool for lifetime estimation was developed and verified. This diagnostic tool can be extended into an impedance-based lifetime model that will be able to predict the remaining useful lifetime of Li-ion batteries for specific grid support applications....

  1. Seeding of silicon by copper ion implantation for selective electroless copper plating

    Energy Technology Data Exchange (ETDEWEB)

    Bhansali, S.; Sood, D.K.; Zmood, R.B. [Microelectronic and Materials Technology Centre, Royal Melbourne Institute of Technolgy, Melbourne, VIC (Australia)

    1993-12-31

    We report on the successful use of copper(self) ion implantation into silicon to seed the electroless plating of copper on silicon (100) surfaces. Copper ions have been implanted to doses of 5E14-6.4E16 ions/cm{sup 2} using a MEEVA ion implanter at extraction voltage of 40kV. Dose was varied in fine steps to determine the threshold dose of 2E15 Cu ions/cm{sup 2} for `seed` formation of copper films on silicon using a commercial electroless plating solution. Plated films were studied with Rutherford backscattering spectrometry, scanning electron microscopy, EDX and profilometry . The adhesion of films was measured by `scotch tape test`. The adhesion was found to improve with increasing dose. However thicker films exhibited rather poor adhesion and high internal stress. SEM results show that the films grow first as isolated islands which become larger and eventually impinge into a continuous film as the plating time is increased. (authors). 5 refs., 1 tab., 3 figs.

  2. Designing Artificial Solid-Electrolyte Interphases for Single-Ion and High-Efficiency Transport in Batteries

    KAUST Repository

    Tu, Zhengyuan

    2017-09-21

    Substrates able to rectify transport of ions based on charge and/or size are ubiquitous in biological systems. Electrolytes and interphases that selectively transport electrochemically active ions are likewise of broad interest in all electrical energy storage technologies. In lithium-ion batteries, electrolytes with single- or near-single-ion conductivity reduce losses caused by ion polarization. In emergent lithium or sodium metal batteries, they maintain high conductivity at the anode and stabilize metal deposition by fundamental mechanisms. We report that 20- to 300-nm-thick, single-ion-conducting membranes deposited at the anode enable electrolytes with the highest combination of cation transference number, ionic conductivity, and electrochemical stability reported. By means of direct visualization we find that single-ion membranes also reduce dendritic deposition of Li in liquids. Galvanostatic measurements further show that the electrolytes facilitate long (3 mAh) recharge of full Li/LiNi0.8Co0.15Al0.05O2 (NCA) cells with high cathode loadings (3 mAh cm−2/19.9 mg cm−2) and at high current densities (3 mA cm−2).

  3. Investigations on transport and storage of high ion beam intensities

    Energy Technology Data Exchange (ETDEWEB)

    Joshi, Ninad Shrikrishna

    2009-08-25

    In the framework of this thesis the intense low energy ion beam transport was investigated. Especially, the beam transport in toroidal magnetic field configurations was discussed, as it may allow the accumulation of high intensive beams in the future. One of the specific tasks is to design an injection system that can be used for the proposed low energy accumulator ring. A simulation code (TBT) was written to describe the particle motion in curved segments. Particle in Cell techniques were utilized to simulate a multi particle dynamics. A possibility of reading an external data file was made available so that a measured distribution can be used to compare simulation results with measured ones. A second order cloud in cell method was used to calculate charge density and in turn to solve Poisson's equation. Further simulations were performed to study the self field effects on beam transport. Experiments were performed to compare the simulation results and gain practical experience. The preparatory experiments consisted of building and characterization of the ion source in a first step. Along with the momentum spectrometer and emittance scanner the beam properties were studied. Low mass ion beams He{sup +} and mixed p, H{sup 2+}, H{sup 3+} beams were analyzed. In the second stage, beams were transported through a solenoid and the phase space distribution was measured as a function of the magnetic field for different beam energies. The phase-space as distributions measured in a first stage were simulated backward and then again forward transported through the solenoid. The simulated results were then compared with the measured distribution. The LINTRA transport program was used. The phase-space distribution was further simulated for transport experiments in a toroidal magnetic field. The transport program that was used to simulate the beam in the toroid was also used to design the injection system. The injection system with its special field configurations was

  4. Verification of high efficient broad beam cold cathode ion source

    Energy Technology Data Exchange (ETDEWEB)

    Abdel Reheem, A. M., E-mail: amreheem2009@yahoo.com [Accelerators and Ion Sources Department, Nuclear Research Center, Atomic Energy Authority, P.N.13759, Cairo (Egypt); Radiation Physics Department, National Center for Radiation Research and Technology (NCRRT), Atomic Energy Authority (AEA), Cairo (Egypt); Ahmed, M. M. [Physics Department, Faculty of Science, Helwan University, Cairo (Egypt); Abdelhamid, M. M.; Ashour, A. H. [Radiation Physics Department, National Center for Radiation Research and Technology (NCRRT), Atomic Energy Authority (AEA), Cairo (Egypt)

    2016-08-15

    An improved form of cold cathode ion source has been designed and constructed. It consists of stainless steel hollow cylinder anode and stainless steel cathode disc, which are separated by a Teflon flange. The electrical discharge and output characteristics have been measured at different pressures using argon, nitrogen, and oxygen gases. The ion exit aperture shape and optimum distance between ion collector plate and cathode disc are studied. The stable discharge current and maximum output ion beam current have been obtained using grid exit aperture. It was found that the optimum distance between ion collector plate and ion exit aperture is equal to 6.25 cm. The cold cathode ion source is used to deposit aluminum coating layer on AZ31 magnesium alloy using argon ion beam current which equals 600 μA. Scanning electron microscope and X-ray diffraction techniques used for characterizing samples before and after aluminum deposition.

  5. Highly charged ions in exotic atoms research at PSI

    Energy Technology Data Exchange (ETDEWEB)

    Anagnostopoulos, D.F.; Biri, S.; Boisbourdain, V.; Demeter, M.; Borchert, G.; Egger, J.P.; Fuhrmann, H.; Gotta, D.; Gruber, A.; Hennebach, M.; Indelicato, P.; Liu, Y.W.; Manil, B.; Markushin, V.E.; Marton, H.; Nelms, N.; Rusi El Hassani, A.J.; Simons, L.M. E-mail: leopold.simons@psi.ch; Stingelin, L.; Wasser, A.; Wells, A.; Zmeskal, J

    2003-05-01

    During their de-excitation, exotic atoms formed in low pressure gases reach a state of high or even complete ionization. X-rays emitted from higher n-states of electron-free atoms have well defined energies with the error originating only from the error in the mass values of the constituent particles. They served as a basis for a new determination of the pion mass as well as for a high precision measurement of the pionic hydrogen ground state shift. The response function of the Bragg spectrometer has been determined with X-rays from completely ionized pionic carbon and with a dedicated electron cyclotron resonance ion trap (ECRIT). A further extension of the ECRIT method implemented in the experiment allows a direct calibration of exotic atom transitions as well as a precise determination of the energy of fluorescence lines.

  6. Study of a High Voltage Ion Engine Power Supply

    Science.gov (United States)

    Stuart, Thomas A.; King, Roger J.; Mayer, Eric

    1996-01-01

    A complete laboratory breadboard version of a ion engine power converter was built and tested. This prototype operated on a line voltage of 80-120 Vdc, and provided output ratings of 1100 V at 1.8 kW, and 250 V at 20 mA. The high-voltage (HV) output voltage rating was revised from the original value of 1350 V at the beginning of the project. The LV output was designed to hold up during a 1-A surge current lasting up to 1 second. The prototype power converter included a internal housekeeping power supply which also operated from the line input. The power consumed in housekeeping was included in the overall energy budget presented for the ion engine converter. HV and LV output voltage setpoints were commanded through potentiometers. The HV converter itself reached its highest power efficiency of slightly over 93% at low line and maximum output. This would dip below 90% at high line. The no-load (rated output voltages, zero load current) power consumption of the entire system was less than 13 W. A careful loss breakdown shows that converter losses are predominately Metal-Oxide-Semiconductor Field Effect Transistor (MOSFET) conduction losses and HV rectifier snubbing losses, with the rectifier snubbing losses becoming predominant at high line. This suggests that further improvements in power efficiency could best be obtained by either developing a rectifier that was adequately protected against voltage overshoot with less snubbing, or by developing a pre-regulator to reduced the range of line voltage on the converter. The transient testing showed the converter to be fully protected against load faults, including a direct short-circuit from the HV output to the LV output terminals. Two currents sensors were used: one to directly detect any core ratcheting on the output transformer and re-initiate a soft start, and the other to directly detect a load fault and quickly shut down the converter for load protection. The finished converter has been extensively fault tested

  7. Detection of decontamination solution chelating agents using ion selective coated-wire electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Banks, Mark Lavior [Arizona Univ., Tucson, AZ (United States)

    1992-01-01

    This thesis explores feasibility of using coated-wire electrodes to measure chelating agent concentration. Chelating agents are often found in radioactive decontamination solutions because they aid in the removal of radionuclides from contaminated surfaces by increasing their solubility. However, this characteristic will also enhance the mobility of the radionuclide and thus its transport out of a waste disposal site. Coated-wire ion selective electrodes, based on a polyvinylchloride membrane using dioctylphthalate as a plasticizer and dinonylnaphthalenesulfonic acid as a counterion, were constructed for five commonly utilized chelating agents (ethylenediaminetetracetic acid (EDTA), nitrilotriacetic acid (NTA), citric acid, oxalic acid and tartaric add). The EDTA and NTA electrodes` calibration characteristics exhibited acceptable behavior in pure standard solutions. From data obtained while using the EDTA and NTA electrodes in a cement environment, further research needs to be done in the area of ion interference.

  8. Preparation, Characterization, and Analytical Application of Ramipril Membrane-Based Ion-Selective Electrode

    Directory of Open Access Journals (Sweden)

    Hassan Arida

    2009-01-01

    Full Text Available The fabrication and electrochemical evaluation of two PVC membrane-based Ion-Selective electrodes responsive for ramipril drug have been proposed. The sensitive membranes were prepared using ramipril-phosphomolibdate and ramipril-tetraphenylborate ion-pair complexes as electroactive sensing materials in plasticized PVC support. The electrodes based on these materials provide near-Nernestian response (sensitivity of 53±0.5–54±0.5 mV/concentration decade covering the concentration range of 1.0×10-2–1.0×10-5 mol L−1 with a detection limit of 3.0×10-6–4.0×10-6 mol L−1. The suggested electrodes have been successfully used in the determination of ramipril drug in some pharmaceutical formulations using direct potentiometry with average recovery of >96% and mean standard deviation of <3% (n=5.

  9. Nano-Composite Cathodes for High Performance Lithium Ion Microbatteries Project

    Data.gov (United States)

    National Aeronautics and Space Administration — TPL Inc. proposes to develop a novel, high performance, nanostructured cathode material for lithium ion (Li-ion) batteries. The proposed approach will modify lithium...

  10. An Integrated Glucose Sensor with an All-Solid-State Sodium Ion-Selective Electrode for a Minimally Invasive Glucose Monitoring System

    Directory of Open Access Journals (Sweden)

    Junko Kojima

    2015-06-01

    Full Text Available We developed a minimally invasive glucose monitoring system that uses a microneedle to permeate the skin surface and a small hydrogel to accumulate interstitial fluid glucose. The measurement of glucose and sodium ion levels in the hydrogel is required for estimating glucose levels in blood; therefore, we developed a small, enzyme-fixed glucose sensor with a high-selectivity, all-solid-state, sodium ion-selective electrode (ISE integrated into its design. The glucose sensor immobilized glucose oxidase showed a good correlation between the glucose levels in the hydrogels and the reference glucose levels (r > 0.99, and exhibited a good precision (coefficient of variation = 2.9%, 0.6 mg/dL. In the design of the sodium ISEs, we used the insertion material Na0.33MnO2 as the inner contact layer and DD16C5 exhibiting high Na+/K+ selectivity as the ionophore. The developed sodium ISE exhibited high selectivity (\\( \\log \\,k^{pot}_{Na,K} = -2.8\\ and good potential stability. The sodium ISE could measure 0.4 mM (10−3.4 M sodium ion levels in the hydrogels containing 268 mM (10−0.57 M KCl. The small integrated sensor (ϕ < 10 mm detected glucose and sodium ions in hydrogels simultaneously within 1 min, and it exhibited sufficient performance for use as a minimally invasive glucose monitoring system.

  11. High temperature electron beam ion source for the production of single charge ions of most elements of the Periodic Table

    CERN Document Server

    Panteleev, V N; Barzakh, A E; Fedorov, D V; Ivanov, V S; Moroz, F V; Orlov, S Y; Seliverstov, D M; Stroe, L; Tecchio, L B; Volkov, Y M

    2003-01-01

    A new type of a high temperature electron beam ion source (HTEBIS) with a working temperature up to 2500 deg. C was developed for production of single charge ions of practically all elements. Off-line tests and on-line experiments making use of the developed ion source coupled with uranium carbide targets of different density, have been carried out. The ionization efficiency measured for stable atoms of many elements varied in the interval of 1-6%. Using the HTEBIS, the yields and on-line production efficiency of neutron rich isotopes of Mn, Fe, Co, Cu, Rh, Pd, Ag, Cd, In, Sn and isotopes of heavy elements Pb, Bi, Po and some others have been determined. The revealed confinement effect of the ions produced in the narrow electron beam inside a hot ion source cavity has been discussed.

  12. Evaluation of the thermal effect on separation selectivity in anion-exchange processes using superheated water ion-exchange chromatography.

    Science.gov (United States)

    Shibukawa, Masami; Taguchi, Akihiko; Suzuki, Yusuke; Saitoh, Kazunori; Hiaki, Toshihiko; Yarita, Takashi

    2012-07-07

    The thermal effect on retention and separation selectivity of inorganic anions and aromatic sulfonate ions in anion-exchange chromatography is studied on a quaternized styrene-divinylbenzene copolymer anion-exchange column in the temperature range of 40-120 °C using superheated water chromatography. The selectivity coefficient for a pair of identically charged anions approaches unity as temperature increases provided the ions have the same effective size, such that the retention of an analyte ion decreases with an increase in temperature when the analyte ion has stronger affinity for the ion-exchanger than that of the eluent counterion, whereas it increases when it has weaker affinity. The change in anion-exchange selectivity with temperature observed with superheated water chromatography has been discussed on the basis of the effect of temperature on hydration of the ions. At elevated temperatures, especially in superheated water, the electrostatic interaction or association of the ions with the fixed ion in the resin phase becomes a predominant factor resulting in a different separation selectivity from that obtained at ambient temperature.

  13. Selective detection of Mg2+ ions via enhanced fluorescence emission using Au–DNA nanocomposites

    Directory of Open Access Journals (Sweden)

    Tanushree Basu

    2017-04-01

    Full Text Available The biophysical properties of DNA-modified Au nanoparticles (AuNPs have attracted a great deal of research interest for various applications in biosensing. AuNPs have strong binding capability to the phosphate and sugar groups in DNA, rendering unique physicochemical properties for detection of metal ions. The formation of Au–DNA nanocomposites is evident from the observed changes in the optical absorption, plasmon band, zeta potential, DLS particle size distribution, as well as TEM and AFM surface morphology analysis. Circular dichroism studies also revealed that DNA-functionalized AuNP binding caused a conformational change in the DNA structure. Due to the size and shape dependent plasmonic interactions of AuNPs (33–78 nm with DNA, the resultant Au–DNA nanocomposites (NCs exhibit superior fluorescence emission due to chemical binding with Ca2+, Fe2+ and Mg2+ ions. A significant increase in fluorescence emission (λex = 260 nm of Au–DNA NCs was observed after selectively binding with Mg2+ ions (20–800 ppm in an aqueous solution where a minimum of 100 ppm Mg2+ ions was detected based on the linearity of concentration versus fluorescence intensity curve (λem = 400 nm. The effectiveness of Au–DNA nanocomposites was further verified by comparing the known concentration (50–120 ppm of Mg2+ ions in synthetic tap water and a real life sample of Gelusil (300–360 ppm Mg2+, a widely used antacid medicine. Therefore, this method could be a sensitive tool for the estimation of water hardness after careful preparation of a suitably designed Au–DNA nanostructure.

  14. Selective detection of Mg2+ions via enhanced fluorescence emission using Au-DNA nanocomposites.

    Science.gov (United States)

    Basu, Tanushree; Rana, Khyati; Das, Niranjan; Pal, Bonamali

    2017-01-01

    The biophysical properties of DNA-modified Au nanoparticles (AuNPs) have attracted a great deal of research interest for various applications in biosensing. AuNPs have strong binding capability to the phosphate and sugar groups in DNA, rendering unique physicochemical properties for detection of metal ions. The formation of Au-DNA nanocomposites is evident from the observed changes in the optical absorption, plasmon band, zeta potential, DLS particle size distribution, as well as TEM and AFM surface morphology analysis. Circular dichroism studies also revealed that DNA-functionalized AuNP binding caused a conformational change in the DNA structure. Due to the size and shape dependent plasmonic interactions of AuNPs (33-78 nm) with DNA, the resultant Au-DNA nanocomposites (NCs) exhibit superior fluorescence emission due to chemical binding with Ca 2+ , Fe 2+ and Mg 2+ ions. A significant increase in fluorescence emission (λ ex = 260 nm) of Au-DNA NCs was observed after selectively binding with Mg 2+ ions (20-800 ppm) in an aqueous solution where a minimum of 100 ppm Mg 2+ ions was detected based on the linearity of concentration versus fluorescence intensity curve (λ em = 400 nm). The effectiveness of Au-DNA nanocomposites was further verified by comparing the known concentration (50-120 ppm) of Mg 2+ ions in synthetic tap water and a real life sample of Gelusil (300-360 ppm Mg 2+ ), a widely used antacid medicine. Therefore, this method could be a sensitive tool for the estimation of water hardness after careful preparation of a suitably designed Au-DNA nanostructure.

  15. Ion-selective optical sensor for continuous on-line monitoring of dialysate sodium during dialysis

    Science.gov (United States)

    Sharma, Manoj K.; Frijns, Arjan J. H.; Mandamparambil, Rajesh; Kooman, Jeroen P.; Smeulders, David M. J.

    2017-02-01

    Patients with end stage renal disease are dependent on dialysis. In most outpatient centers, the dialysate is prepared with a fixed electrolyte concentration without taking into account the inter-individual differences of essential electrolytes (sodium, potassium and calcium). This one-size fits all approach can lead to acute and chronic cardiovascular complications in dialysis patients. On-line monitoring of these essential electrolytes is an important physiological step towards patient specific dialysate leading to individualized treatment. Currently, changes in electrolyte concentrations are indirectly measured by conductivity measurements, which are not ion- specific. In this paper, we present a novel optical sensor for on-line monitoring of sodium concentrations in dialysate. This sensor is ion-specific and can detect up to a single ion. The working principle is based on the selective fluorescence quenching of photo-induced electron transfer (PET) molecules. The PET molecules when complexed with sodium ions start fluorescing upon laser excitation. The emission intensity is directly correlated to the sodium concentration. To prove the working principle, a micro-optofluidic device has been fabricated in polydimethylsiloxane (PDMS) with integrated optical fibers for fluorescence light collection. The PET molecules are covalently grafted in the PDMS microchannel for continuous monitoring of the sodium dialysate concentrations. The experimental setup consists of a laser module (λ=450nm) operating at 4.5mW, a syringe pump to precisely control the sample flow and a spectrometer for fluorescence collection. The performance of the sensor has been evaluated for sodium ions ranging from 0-50mM. A clear signal and good response time was observed.

  16. High ion conducting polymer nanocomposite electrolytes using hybrid nanofillers.

    Science.gov (United States)

    Tang, Changyu; Hackenberg, Ken; Fu, Qiang; Ajayan, Pulickel M; Ardebili, Haleh

    2012-03-14

    There is a growing shift from liquid electrolytes toward solid polymer electrolytes, in energy storage devices, due to the many advantages of the latter such as enhanced safety, flexibility, and manufacturability. The main issue with polymer electrolytes is their lower ionic conductivity compared to that of liquid electrolytes. Nanoscale fillers such as silica and alumina nanoparticles are known to enhance the ionic conductivity of polymer electrolytes. Although carbon nanotubes have been used as fillers for polymers in various applications, they have not yet been used in polymer electrolytes as they are conductive and can pose the risk of electrical shorting. In this study, we show that nanotubes can be packaged within insulating clay layers to form effective 3D nanofillers. We show that such hybrid nanofillers increase the lithium ion conductivity of PEO electrolyte by almost 2 orders of magnitude. Furthermore, significant improvement in mechanical properties were observed where only 5 wt % addition of the filler led to 160% increase in the tensile strength of the polymer. This new approach of embedding conducting-insulating hybrid nanofillers could lead to the development of a new generation of polymer nanocomposite electrolytes with high ion conductivity and improved mechanical properties. © 2012 American Chemical Society

  17. A calixarene-based ion-selective electrode for thallium(I) detection

    Energy Technology Data Exchange (ETDEWEB)

    Chester, Ryan [Nanochemistry Research Institute, Department of Chemistry, Curtin University, GPO Box U1987, Perth, Western Australia 6845 (Australia); Sohail, Manzar [Faculty of Science, Health, Education and Engineering, University of the Sunshine Coast, Locked Bag 4, Maroochydore DC, Queensland 4556 (Australia); Ogden, Mark I.; Mocerino, Mauro [Nanochemistry Research Institute, Department of Chemistry, Curtin University, GPO Box U1987, Perth, Western Australia 6845 (Australia); Pretsch, Ernö [ETH Zürich, Institute of Biogeochemistry and Pollutant Dynamics (IBP), Universitätstrasse 16, CH-8092, Zürich (Switzerland); De Marco, Roland, E-mail: rdemarc1@usc.edu.au [Nanochemistry Research Institute, Department of Chemistry, Curtin University, GPO Box U1987, Perth, Western Australia 6845 (Australia); Faculty of Science, Health, Education and Engineering, University of the Sunshine Coast, Locked Bag 4, Maroochydore DC, Queensland 4556 (Australia)

    2014-12-03

    Highlights: • Tuning of metal binding cavities in thallium(I) calixarene ionophores. • Novel calixarene-based ionophores with improved selectivity for thallium(I). • Sandwich membrane characterization of thallium(I) binding in novel calixarenes. • Improved selectivity and sensitivity with novel thallium(I) calixarene ionophores. • Solid contact ion-selective electrodes for novel thallium(I) calixarene ionophores. - Abstract: Three new calixarene Tl{sup +} ionophores have been utilized in Tl{sup +} ion-selective electrodes (ISEs) yielding Nernstian response in the concentration range of 10{sup −2}–10{sup −6} M TlNO{sub 3} with a non-optimized filling solution in a conventional liquid contact ISE configuration. The complex formation constants (log β{sub IL}) for two of the calixarene derivatives with thallium(I) (i.e. 6.44 and 5.85) were measured using the sandwich membrane technique, with the other ionophore immeasurable due to eventual precipitation of the ionophore during these long-term experiments. Furthermore, the unbiased selectivity coefficients for these ionophores displayed excellent selectivity against Zn{sup 2+}, Ca{sup 2+}, Ba{sup 2+}, Cu{sup 2+}, Cd{sup 2+} and Al{sup 3+} with moderate selectivity against Pb{sup 2+}, Li{sup +}, Na{sup +}, H{sup +}, K{sup +}, NH{sub 4}{sup +} and Cs{sup +}, noting that silver was the only significant interferent with these calixarene-based ionophores. When optimizing the filling solution in a liquid contact ISE, it was possible to achieve a lower limit of detection of approximately 8 nM according to the IUPAC definition. Last, the new ionophores were also evaluated in four solid-contact (SC) designs leading to Nernstian response, with the best response noted with a SC electrode utilizing a gold substrate, a poly(3-octylthiophene) (POT) ion-to-electron transducer and a poly(methyl methacrylate)–poly(decyl methacrylate) (PMMA–PDMA) co-polymer membrane. This electrode exhibited a slope of 58.4 mV decade

  18. Copper (II) ion selective liquid membrane electrode based on new Schiff base carrier.

    Science.gov (United States)

    Sadeghi, Susan; Vardini, Mohammad Taghi; Naeimi, Hossein

    2006-01-01

    Cu2+ selective PVC membrane electrode based on new Schiff base 2, 2'-[1,9 nonanediyl bis (nitriloethylidyne)]-bis-(1-naphthol) as a selective carrier was constructed. The electrode exhibited a linear potential response within the activity range of 1.0 x 10(-6) - 5.0 x 10(-3) moll(-1) with a Nernstian slope of 29 +/- 1 mV decade(-1) of Cu2+ activity and a limit of detection 8.0 x 10(-7) mol l(-1). The response time of the electrode was fast, 10 s, and stable potentials were obtained within the pH range of 3.5- 6.5. The potentiometric selectivity coefficients were evaluated using two solution method and revealed no important interferences except for Ag+ ion. The proposed electrode was applied as an indicator electrode to potentiometric titration of Cu2+ ions and determination of Cu2+ content in real samples such as black tea leaves and multivitamin capsule.

  19. Determination of Cd2+ in aqueous solution using polyindole-Ce(IV) vanadophosphate conductive nanocomposite ion-selective membrane electrode

    Science.gov (United States)

    Khan, Asif Ali; Quasim Khan, Mohd; Hussain, Rizwan

    2017-09-01

    In the present study an organic-inorganic nanocomposite ion exchanger Polyindole-Ce(IV) vanadophosphate (PIn-CVP) was synthesized via sol-gel process showing excellent ion exchange capacity (IEC‒1.90 meqg-1). The material was characterized by SEM, TEM, XRD, FTIR, and TGA. A heterogeneous ion exchange membrane of PIn-CVP (IEC‒0.90 meqg-1) was also prepared by solution casting method. PIn-CVP shows high electrical conductivity (5.5  ×  10-2 S cm-1) and it is stable up to 120 °C under ambient conditions. Cd2+ selective membrane electrode was fabricated and its linear working range (3.98  ×  10-7 M to 1.0  ×  10-1 M), response time (25 s), Nerstian slope 25.00 mV dec-1 and working pH range (4-7) were calculated. It was employed as an indicator electrode in the potentiometric titration of Cd2+.

  20. Improving the Selectivity of the ISOLDE Resonance Ionization Laser Ion Source and In-Source Laser Spectroscopy of Polonium

    CERN Document Server

    Fink, Daniel Andreas; Jochim, Selim

    Exotic atomic nuclei far away from stability are fascinating objects to be studied in many scientic elds such as atomic-, nuclear-, and astrophysics. Since these are often short-lived isotopes, it is necessary to couple their production with immediate extraction and delivery to an experiment. This is the purpose of the on-line isotope separator facility, ISOLDE, at CERN. An essential aspect of this laboratory is the Resonance Ionization Laser Ion Source (RILIS) because it provides a fast and highly selective means of ionizing the reaction products. This technique is also a sensitive laser-spectroscopy tool for the development and improvement of electron excitation schemes for the resonant laser photoionization and the study of the nuclear structure or fundamental atomic physics. Each of these aspects of the RILIS applications are subjects of this thesis work: a new device for the suppression of unwanted surface ionized contaminants in RILIS ion beams, known as the Laser Ion Source and Trap (LIST), was impleme...

  1. High intensity production of high and medium charge state uraniumand other heavy ion beams with VENUS

    Energy Technology Data Exchange (ETDEWEB)

    Leitner, Daniela; Galloway, Michelle L.; Loew, Timothy J.; Lyneis, Claude M.; Rodriguez, Ingrid Castro; Todd, Damon S.

    2007-11-15

    The next generation, superconducting ECR ion source VENUS(Versatile ECR ion source for NUclear Science) started operation with 28GHzmicrowave heating in 2004. Since then it has produced world recordion beam intensities. For example, 2850 e mu A of O6+, 200 e mu A of U33+or U34+, and in respect to high charge state ions, 1 e mu A of Ar18+, 270e mu A of Ar16+, 28 e mu A of Xe35+ and 4.9 e mu A of U47+ have beenproduced. A brief overview of the latest developments leading to theserecord intensities is given and the production of high intensity uraniumbeams is discussed in more detail.

  2. Selective electrochemical sensor for copper (II) ion based on chelating ionophores

    Energy Technology Data Exchange (ETDEWEB)

    Singh, Ashok Kumar [Department of Chemistry, Indian Institute of Technology at Roorkee, Roorkee 247667 (India)]. E-mail: akscyfcy@iitr.ernet.in; Mehtab, Sameena [Department of Chemistry, Indian Institute of Technology at Roorkee, Roorkee 247667 (India); Jain, Ajay Kumar [Department of Chemistry, Indian Institute of Technology at Roorkee, Roorkee 247667 (India)

    2006-08-04

    Plasticized membranes using 3-(2-pyridinyl)-2H-pyrido[1,2,-a]-1,3,5-triazine-2,4(3H)-dithione (L {sub 1}) and acetoacetanilide (L {sub 2}) have been prepared and explored as Cu{sup 2+}-selective sensors. Effect of various plasticizers, viz. chloronaphthalene (China), benzyl acetate (BA), o-nitrophenyloctyl ether (o-NPOE), and anion excluders, sodium tetraphenylborate (NaTPB) and oleic acid (OA) was studied in detail and improved performance was observed at several instances. Optimum performance was observed with dithione derivative (L {sub 1}) having a membrane composition of L {sub 1} (5):PVC (120):o-NPOE (240):OA (10). The sensor works satisfactorily in the concentration range 5.0 x 10{sup -8} to 1.0 x 10{sup -2} M (detection limit 4.0 x 10{sup -8} M) with a Nernstian slope of 29.5 mV decade{sup -1} of activity. Wide pH range (3.0-9.5), fast response time (12 s), non-aqueous tolerance (up to 20%) and adequate shelf life (4 months) indicate the vital utility of the proposed sensor. The potentiometric selectivity coefficient values as determined by match potential method (MPM) indicate good response for Cu{sup 2+} in presence of interfering ions. The proposed electrode comparatively shows good selectivity with respect to alkali, alkaline earth, transition and some rare earth metals ions. The electrode was used for the determination of copper in different milk powder, water samples and as indicator electrode in potentiometric titration of copper ion with EDTA.

  3. Uncharted Frontiers in the Spectroscopy of Highly Charged Ions

    CERN Document Server

    Beiersdorfer, P; Crespo, J; Kim, S H; Neill, P; Utter, S; Widmann, K

    2000-01-01

    The development of novel techniques is critical for maintaining a state-of-the-art core competency in atomic physics and readiness for evolving programmatic needs. We have carried out a three-year effort to develop novel spectroscopic instrumentation that added new dimensions to our capabilities for measuring energy levels, radiative transition probabilities, and electron-ion excitation processes. The new capabilities created were in areas that heretofore had been inaccessible to scientific scrutiny and included high-resolution spectroscopy of hard x rays, femtosecond lifetime measurements, measurements of transition probabilities of long-lived metastable levels, polarization spectroscopy, ultra-precise determinations of energy levels, and the establishment of absolute wavelength standards in x-ray spectroscopy. Instrumentation developed during the period included a transmission-type crystal spectrometer, a flat-field EUV spectrometer, and the development and deployment of absolutely calibrated monolithic cry...

  4. High-Energy Ion Linacs Based on Spoke Cavities

    CERN Document Server

    Shephard, K W; Ostromov, P N

    2003-01-01

    The applicability of superconducting TEM-class spoke cavities to high-energy ion linacs is discussed, and detailed designs for two TEM-class, triple-spoke-loaded superconducting niobium resonant cavities are presented. The 345 MHz cavities have a velocity range of 0.4

  5. Selective discrimination of small hydrophobic biomolecules based on ion-current rectification in conically shaped nanochannel.

    Science.gov (United States)

    Guo, Zhijun; Wang, Jiahai; Wang, Erkang

    2012-01-30

    In this study, based on ion-current rectification in the conically shaped nanochannel embedded in polyethylene terephthalate (PET) membrane, we have selectively discriminated three small biomolecules. Because three positive biomolecules (Hoechst 33342, Propidium and Bupivacaine) have different hydrophobicities, their interactions with inside wall of the conical nanochannel are different and their binding affinities can be derived from Langmuir absorption model. Therefore, we can successfully discriminate these small biomolecules. The highest binding constant was obtained for the small molecule with highest hydrophobicity. Another interesting result is that the detection limit for the small molecule with the highest binding constant shifts to submicromole. Copyright © 2011 Elsevier B.V. All rights reserved.

  6. Histidine–dialkoxyanthracene dyad for selective and sensitive detection of mercury ions

    KAUST Repository

    Patil, Sachin

    2017-12-18

    Histidine-dialkoxyanthracene (HDA) was synthesised as a turn off type fluorescent sensor for fast and sensitive detection of mercury ions (Hg2+) in aqueous media. The two histidine moieties act as ‘claws’ to selectively complex Hg2+. The binding ratio of HDA to Hg2+ was 1:1 (metal-to-ligand ratio). The association constant for Hg2+ towards the receptor HDA obtained from Benesi–Hildebrand plot was found to be 3.22 × 104 M−1 with detection limit as low as 4.7 nM (0.94 μg/L).

  7. Borophene as an extremely high capacity electrode material for Li-ion and Na-ion batteries.

    Science.gov (United States)

    Zhang, Xiaoming; Hu, Junping; Cheng, Yingchun; Yang, Hui Ying; Yao, Yugui; Yang, Shengyuan A

    2016-08-18

    "Two-dimensional (2D) materials as electrodes" is believed to be the trend for future Li-ion and Na-ion battery technologies. Here, by using first-principles methods, we predict that the recently reported borophene (2D boron sheets) can serve as an ideal electrode material with high electrochemical performance for both Li-ion and Na-ion batteries. The calculations are performed on two experimentally stable borophene structures, namely β12 and χ3 structures. The optimized Li and Na adsorption sites are identified, and the host materials are found to maintain good electric conductivity before and after adsorption. Besides advantages including small diffusion barriers and low average open-circuit voltages, most remarkably, the storage capacity can be as high as 1984 mA h g(-1) in β12 borophene and 1240 mA h g(-1) in χ3 borophene for both Li and Na, which are several times higher than the commercial graphite electrode and are the highest among all the 2D materials discovered to date. Our results highly support that borophenes can be appealing anode materials for both Li-ion and Na-ion batteries with extremely high power density.

  8. Selected methods of electron-and ion-diagnostics in tokamak scrape-off-layer

    Directory of Open Access Journals (Sweden)

    Sadowski Marek J.

    2015-06-01

    Full Text Available This invited paper considers reasons why exact measurements of fast electron and ion losses in tokamaks, and particularly i n a scrape-off-layer and near a divertor region, are necessary in order to master nuclear fusion energy production. Attention is also paid to direct measurements of escaping fusion products from D-D and D-T reactions, and in particular of fast alphas which might be used for plasma heating. The second part describes the generation of so-called runaway and ripple-born electrons which might induce high energy losses and cause severe damages of internal walls in fusion facilities. Advantages and disadvantages of different diagnostic methods applied for studies of such fast electrons are discussed. Particular attention is paid to development of a direct measuring technique based on the Cherenkov effect which might be induced by fast electrons in appropriate radiators. There are presented various versions of Cherenkov-type probes which have been developed by the NCBJ team and applied in different tokamak experiments. The third part is devoted to direct measurements of fast ions (including those produced by the nuclear fusion reactions which can escape from a high-temperature plasma region. Investigation of fast fusion-produced protons from tokamak discharges is reported. New ion probes, which were developed by the NCBJ team, are also presented. For the first time there is given a detailed description of an ion pinhole camera, which enables irradiation of several nuclear track detectors during a single tokamak discharge, and a miniature Thomson-type mass-spectrometer, which can be used for ion measurements at plasma borders.

  9. Stuides on a Pb2+-selective electrode with a macrocyclic liquid membrane. Potentiometric determination of Pb2+ ions

    Directory of Open Access Journals (Sweden)

    MARIAN ISVORANU

    2006-12-01

    Full Text Available This paper presents experimental and theoretical data regarding the design, characterization and analytical applications of a non-expensive, liquid-membrane ion-selective electrode for Pb2+ ions. The membrane is a solution of the active complex formed by Pb2+ ions with dibenzo-18-crown-6-ionophore (DB-[18]-C-6 extracted in propylene carbonate (PC. The sucessful application of the developed electrode for the determination of Pb2+ ions in aqueos solution samples by direct potentiometry and potentiometric titration is presented. For the presented analytical results, there are insignificant systematic errors between the direct potentiometric method with the developed ion-selective electrode and atomic absorption spectrometry.

  10. Pyrene-Phosphonate Conjugate: Aggregation-Induced Enhanced Emission, and Selective Fe3+Ions Sensing Properties.

    Science.gov (United States)

    Padghan, Sachin D; Bhosale, Rajesh S; Bhosale, Sidhanath V; Antolasic, Frank; Al Kobaisi, Mohammad; Bhosale, Sheshanath V

    2017-08-29

    A new pyrene-phosphonate colorimetric receptor 1 has been designed and synthesized in a one-step process via amide bond formation between pyrene butyric acid chloride and phosphonate-appended aniline. The pyrene-phosphonate receptor 1 showed aggregation-induced enhanced emission (AIEE) properties in water/acetonitrile (ACN) solutions. Dynamic light scattering (DLS) characterization revealed that the aggregates of receptor 1 at 80% water fraction have an average size of ≈142 nm. Field emission scanning electron microscopy (FE-SEM) analysis confirmed the formation of spherical aggregates upon solvent evaporation. The sensing properties of receptor 1 were investigated by UV-vis, fluorescence emission spectroscopy, and other optical methods. Among the tested metal ions, receptor 1 is capable of recognizing the Fe 3+ ion selectively. The changes in spectral measurements were explained on the basis of complex formation. The composition of receptor 1 and Fe 3+ ions was determined by using Job's plot and found to be 1:1. The receptor 1 -Fe 3 + complex showed a reversible UV-vis response in the presence of EDTA.

  11. Adsorption affinity and selectivity of 3-ureidopropyltriethoxysilane grafted oil palm empty fruit bunches towards mercury ions.

    Science.gov (United States)

    Kunjirama, Magendran; Saman, Norasikin; Johari, Khairiraihanna; Song, Shiow-Tien; Kong, Helen; Cheu, Siew-Chin; Lye, Jimmy Wei Ping; Mat, Hanapi

    2017-06-01

    This study was conducted to investigate the potential application of oil palm empty fruit branches (OPEFB) as adsorbents to remove organic methylmercurry, MeHg(II), and inorganic Hg(II) from aqueous solution. The OPEFB was functionalized with amine containing ligand namely 3-ureidopropyltriethoxysilane (UPTES) aiming for better adsorption performance towards both mercury ions. The adsorption was found to be dependent on initial pH, initial concentraton, temperatures, and contact time. The maximum adsorption capacities (Q m.exp ) of Hg(II) adsorption onto OPEFB and UPTES-OPEFB were 0.226 and 0.773 mmol/g, respectively. The Q m.exp of MeHg(II) onto OPEFB, however, was higher than UPTES-OPEFB. The adsorption kinetic data obeyed the Elovich model and the adsorption was controlled by the film-diffusion step. The calculated thermodynamic parameters indicate an endothermic adsorption process. Adsorption data analysis indicates that the adsorption mechanism may include ion-exchange, complexation, and physisorption interactions. The potential applications of adsorbents were demonstrated using oilfield produced water and natural gas condensate. The UPTES-OPEFB offered higher selectivity towards both mercury ions than OPEFB. The regenerability studies indicated that the adsorbent could be reused for multiple cycles.

  12. Preparation and characterization of electrically conducting polypyrrole Sn(IV phosphate cation-exchanger and its application as Mn(II ion selective membrane electrode

    Directory of Open Access Journals (Sweden)

    A.A. Khan

    2011-10-01

    Full Text Available Polypyrrole Sn(IV phosphate, an organic–inorganic composite cation-exchanger was synthesized via sol-gel mixing of an organic polymer, polypyrrole, into the matrices of the inorganic precipitate of Sn(IV phosphate. The physico-chemical properties of the material were determined using Atomic Absorption Spectrometry (AAS, CHN elemental analysis (inductively coupled plasma mass spectrometry, ICP-MS, UV–VIS spectrophotometry, FTIR (Fourier Transform Infra-Red, SEM (Scanning Electron Microscopy, TGA–DTA (Thermogravimetric Analysis–Differential Thermal Analysis, and XRD (X-ray diffraction. Ion-exchange behavior was observed to characterize the material. On the basis of distribution studies, the material was found to be highly selective for toxic heavy metal ion Mn2+. Due to its selective nature, the material was used as an electroactive component for the construction of an ion-selective membrane electrode. The proposed electrode shows fairly good discrimination of mercury ion over several other inorganic ions. The analytical utility of this electrode was established by employing it as an indicator electrode in electrometric titrations for Mn(II in water.

  13. Using the Doubly Charged Selected Ion Coupled with MS/MS Fragments Monitoring (DCSI-MS/MS Mode for the Identification of Gelatin Species

    Directory of Open Access Journals (Sweden)

    Xian-Long Cheng

    2014-01-01

    Full Text Available In electrospray ionization (ESI mode, peptides and proteins can be multiply charged ions; in this situation a doubly charged selected ion (DCSI coupled with mass spectrometry (MS/MS fragments monitoring (DCSI-MS/MS method is the most suitable scanning mode to detect known peptides in complex samples when an ion-trap mass spectrometer is the instrument used for the analysis. In this mode, the MS detector is programmed to only select a doubly charged ion as a precursor and to perform continuous MS/MS on one or more of the selected precursors, either during a specific time interval or along the whole chromatographic run. Gelatin is a mixture of high molecular weight polypeptides from the hydrolysis of collagen. In this study, the DCSI-MS/MS monitoring mode was applied to the detection of previously characterized species-specific peptides from different gelatins. The proposed methodology makes use of tryptic digestion for sample preparation and peptide separation and identification by rapid resolution liquid chromatography coupled to an ion trap working in the DCSI-MS/MS mode for the analysis. This methodology was applied to the differential classification of five commercial, homological species of gelatins and proved to be an excellent tool for gelatin product authentication.

  14. 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.

  15. Swift heavy ion induced single event upsets in high density UV-EPROM's

    Energy Technology Data Exchange (ETDEWEB)

    Dahiwale, S.S. [Department of Physics, University of Pune, Pune 7 (India); Shinde, N.S. [Department of Chemical Engineering, Mie University (Japan); Kanjilal, D. [Inter University Accelerator Center, New Delhi (India); Bhoraskar, V.N. [Department of Physics, University of Pune, Pune 7 (India); Dhole, S.D. [Department of Physics, University of Pune, Pune 7 (India)], E-mail: sanjay@physics.unipune.ernet.in

    2008-04-15

    A few high density UV-EPROM's (32Kb x 8) were irradiated with 5.41 MeV energy {alpha}-particles with fluences from 10{sup 4} to 10{sup 8} alphas/cm{sup 2} and 100 MeV nickel, iodine and silver ions for low fluences between 5 x 10{sup 7} and 10{sup 8} ions/cm{sup 2}. The energy and ion species was selected on the basis of predicted threshold values of linear energy transfer (LET) in silicon. The program which was stored in the memory found to be changed from 0 to 1 and 1 to 0 state, respectively. On the basis of changed states, the cross-sections ({sigma}) were calculated to investigate the single event effects/upsets. No upset was observed in case of {alpha}-particle since it has very low LET, but the SEU cross-section found to be more in case of Iodine i.e. 2.29 x 10{sup -3} cm{sup 2} than that of nickel, 2.12 x 10{sup -3} cm{sup 2} and silver, 2.26 x 10{sup -3}. This mainly attributes that LET for iodine is more as compared to silver and nickel ions, which deposits large amount of energy near the sensitive node of memory cell in the form of electron-hole pairs required to change the state. These measured SEU cross-section were also compared with theoretically predicted values along with the Weibull distribution fit to the ion induced experimental SEU data. The theoretical predicted SEU cross-section 3.27 x 10{sup -3} cm{sup 2} found to be in good agreement with the measured SEU cross-section.

  16. Highly Selective Hydroformylation of the Cinchona Alkaloids

    NARCIS (Netherlands)

    Lambers, Marielle; Beijer, Felix H.; Padron, José M.; Toth, Imre; Vries, Johannes G. de

    2002-01-01

    The four naturally occurring cinchona alkaloids were subjected to hydroformylation to create an extra functional group that allows immobilization. Cinchonidine, quinine, and quinidine, could be hydroformylated with virtually complete terminal selectivity, using a rhodium/tetraphosphite catalyst. The

  17. Efficient and Highly Aldehyde Selective Wacker Oxidation

    KAUST Repository

    Teo, Peili

    2012-07-06

    A method for efficient and aldehyde-selective Wacker oxidation of aryl-substituted olefins using PdCl 2(MeCN) 2, 1,4-benzoquinone, and t-BuOH in air is described. Up to a 96% yield of aldehyde can be obtained, and up to 99% selectivity can be achieved with styrene-related substrates. © 2012 American Chemical Society.

  18. High energy ion hit technique to local area using microbeam

    Energy Technology Data Exchange (ETDEWEB)

    Tanaka, Ryuichi; Kamiya, Tomihiro; Suda, Tamotsu; Sakai, Takuro; Hirao, Toshio; Kobayashi, Yasuhiko; Watanabe, Hiroshi [Japan Atomic Energy Research Inst., Takasaki, Gunma (Japan). Takasaki Radiation Chemistry Research Establishment

    1997-03-01

    Single energetic ion hit technique has been developed as an application of ion microbeam technique, in order to study the effect of local damage or injury to materials and living organisms. The overall performance is basically defined by those of separate techniques: microbeam formation, microbeam positioning, single ion detection, detection signal processing, hit timing control, and hit verification. Recent progress on the developments of these techniques at JAERI-TIARA facility are reviewed. (author)

  19. Hydrogenated carbon clusters produced by highly charged ion impact on solid C-84

    NARCIS (Netherlands)

    Schlatholter, T; Newman, MW; Niedermayr, TR; Machicoane, GA; McDonald, JW; Schenkel, T; Hoekstra, R; Hamza, AV

    2000-01-01

    The emission of small (hydrogenated) carbon cluster ions: CnHm+ (n = 2-22) upon highly charged Xeq+ (q = 20- 14) impact on C-84 surfaces is studied by means of time-of-flight secundary ion mass spectrometry. The respective stage of hydrogenation/protonation of a certain carbon cluster ion C-n(+) is

  20. Techniques and mechanisms applied in electron cyclotron resonance sources for highly charged ions

    NARCIS (Netherlands)

    Drentje, AG

    Electron cyclotron resonance ion sources are delivering beams of highly charged ions for a wide range of applications in many laboratories. For more than two decades, the development of these ion sources has been to a large extent an intuitive and experimental enterprise. Much effort has been spent

  1. Ion-selective piezoelectric sensor for niacinamide assay in serum and urine.

    Science.gov (United States)

    Long, Y; Li, W; Nie, L; Yao, S

    2001-01-01

    An ion-selective piezoelectric (ISP) sensor was successfully applied for the determination of niacinamide in serum and urine. By coating a polyvinylchloride membrane containing niacinamide-silicotungstate on one electrode of a thickness-shear mode piezoelectric quartz crystal, the ISP device can adsorb niacinamide selectively. The amount of coating applied to the crystal was calculated from the Sauerbrey equation by monitoring the frequency change. The logarithm of the frequency shift was linear with the logarithm of niacinamide concentration over the range from 1.0 x 10(-9) to 1.0 x 10(-3) M with a detection limit of 1.0 x 10(-9) M at pH 7.0. Influencing factors were investigated and optimized. The results for real samples obtained by the proposed method were in good agreement with those obtained by the conventional methods.

  2. High throughput electrophysiology: new perspectives for ion channel drug discovery

    DEFF Research Database (Denmark)

    Willumsen, Niels J; Bech, Morten; Olesen, Søren-Peter

    2003-01-01

    Proper function of ion channels is crucial for all living cells. Ion channel dysfunction may lead to a number of diseases, so-called channelopathies, and a number of common diseases, including epilepsy, arrhythmia, and type II diabetes, are primarily treated by drugs that modulate ion channels...... channel targets accessible for drug screening. Specifically, genuine HTS parallel processing techniques based on arrays of planar silicon chips are being developed, but also lower throughput sequential techniques may be of value in compound screening, lead optimization, and safety screening....... The introduction of new powerful HTS electrophysiological techniques is predicted to cause a revolution in ion channel drug discovery....

  3. High voltage spinel oxides for Li-ion batteries: From the material research to the application

    Science.gov (United States)

    Patoux, Sébastien; Daniel, Lise; Bourbon, Carole; Lignier, Hélène; Pagano, Carole; Le Cras, Frédéric; Jouanneau, Séverine; Martinet, Sébastien

    Li-ion batteries are already used in many nomad applications, but improvement of this technology is still necessary to be durably introduced on new markets such as electric vehicles (EVs), hybrid electric vehicles (HEVs) or eventually photovoltaic solar cells. Modification of the nature of the active materials of electrodes is the most challenging and innovative aspect. High voltage spinel oxides for Li-ion batteries, with general composition LiMn 2- xM xO 4 (M a transition metal element), may be used to face increasing power source demand. It should be possible to obtain up to 240 Wh kg -1 at cell level when combining a nickel manganese spinel oxide with graphite (even more with silicon/carbon nanocomposites at the anode). Specific composition and material processing have to be selected with care, as discussed in this paper. It is demonstrated that 'LiNi 0.5Mn 1.5O 4' and LiNi 0.4Mn 1.6O 4 have remarkable properties such as high potential, high energy density, good cycle life and high rate capability. Choice of the electrolyte is also of primary importance in order to prevent its degradation at high voltage in contact with active surfaces. We showed that a few percents of additive in the electrolyte were suitable for protecting the positive electrode/electrolyte interface, and reducing the self-discharge. High voltage materials are also possibly interesting to be used in safe and high power Li-ion cells. In this case, the negative electrode may be made of Li 4Ti 5O 12 or TiO 2 to give a '3 V' system.

  4. Highly sensitive label-free fluorescent detection of Hg2+ ions by DNA molecular machine-based Ag nanoclusters.

    Science.gov (United States)

    Yin, Jinjin; He, Xiaoxiao; Jia, Xuekun; Wang, Kemin; Xu, Fengzhou

    2013-04-21

    We present here a highly selective and sensitive label-free method to detect Hg(2+) ions in aqueous solution by using DNA molecular machine-based fluorescent Ag nanoclusters (AgNCs). This mechanism is based on the Hg(2+) ions triggering machine-like operations of DNA and the "product" of the machine being used to stabilize fluorescent AgNCs. In this method, a tailored DNA, containing a sequence for Hg(2+) ions recognition, a sequence-specific nicking site for Nb BbvC I and a sequence complementary to the DNA as a template for the synthesis of fluorescent AgNCs, was firstly designed. In the presence of Hg(2+) ions, the machine's function operations were triggered. A series of machine-like operations, including replication, scission, and displacement then occurred with the addition of polymerase/dNTPs/Nb BbvC I, which manufactured lots of "product" DNA. The "product" DNA could act as a template for the preparation of fluorescent AgNCs. Thus the fluorescence of the AgNCs could be used as a signal transduction of this DNA machine, which was related to the concentration of the Hg(2+) ions. The repeated synthesis of the "product" and its template effect for AgNCs synthesis led to signal amplification in the assay of Hg(2+) ions. A linear response to the concentration of Hg(2+) ions was observed in the range from 0.08 nM to 20 nM and a detection limit of 0.08 nM was obtained. By contrast, the operation of the machine could not be executed in an Hg(2+) ion-free system. Moreover, the detection was not only label-free but also specific for Hg(2+) ions without being affected by other metal ions.

  5. The FRS Ion Catcher - A facility for high-precision experiments with stopped projectile and fission fragments

    Science.gov (United States)

    Plaß, W. R.; Dickel, T.; Purushothaman, S.; Dendooven, P.; Geissel, H.; Ebert, J.; Haettner, E.; Jesch, C.; Ranjan, M.; Reiter, M. P.; Weick, H.; Amjad, F.; Ayet, S.; Diwisch, M.; Estrade, A.; Farinon, F.; Greiner, F.; Kalantar-Nayestanaki, N.; Knöbel, R.; Kurcewicz, J.; Lang, J.; Moore, I.; Mukha, I.; Nociforo, C.; Petrick, M.; Pfützner, M.; Pietri, S.; Prochazka, A.; Rink, A.-K.; Rinta-Antila, S.; Schäfer, D.; Scheidenberger, C.; Takechi, M.; Tanaka, Y. K.; Winfield, J. S.; Yavor, M. I.

    2013-12-01

    At the FRS Ion Catcher at GSI, projectile and fission fragments are produced at relativistic energies, separated in-flight, range-focused, slowed down and thermalized in a cryogenic stopping cell. A multiple-reflection time-of-flight mass spectrometer (MR-TOF-MS) is used to perform direct mass measurements and to provide an isobarically clean beam for further experiments, such as mass-selected decay spectroscopy. A versatile RF quadrupole transport and diagnostics unit guides the ions from the stopping cell to the MR-TOF-MS, provides differential pumping, ion identification and includes reference ion sources. The FRS Ion Catcher serves as a test facility for the Low-Energy Branch of the Super-FRS at the Facility for Antiproton and Ion Research (FAIR), where the cryogenic stopping cell and the MR-TOF-MS will be key devices for the research with stopped projectile and fission fragments that will be performed with the experiments MATS and LaSpec. Off-line tests of the stopping cell yield a combined ion survival and extraction efficiency for 219Rn ions of about 30% and an extraction time of about 25 ms. The stopping cell and the MR-TOF-MS were commissioned on-line as part of the FRS Ion Catcher. For the first time, a stopping cell for exotic nuclei was operated on-line at cryogenic temperatures. Using a gas density almost two times higher than ever reached before for a stopping cell with RF ion repelling structures, various 238U projectile fragments were thermalized and extracted with very high efficiency. Direct mass measurements of projectile fragments were performed with the MR-TOF-MS, among them the nuclide 213Rn with a half-life of 19.5 ms only.

  6. Paper-based ion concentration polarization device for selective preconcentration of muc1 and lamp-2 genes

    Science.gov (United States)

    Son, Seok Young; Lee, Hyomin; Kim, Sung Jae

    2017-12-01

    Recently, novel biomolecules separation and detection methods based on ion concentration polarization (ICP) phenomena have been extensively researched due to its high amplification ratio and high-speed accumulation. Despite of these bright advances, the fabrication of conventional ICP devices still have complicated and times-consuming tasks. As an alternative platform, a paper have been recently used for the identical ICP operations. In this work, we demonstrated the selective preconcentration of a muc1 gene fragment as human breast cancer marker and a lamp-2 gene fragment as the cause of Danon disease in paper-based ICP devices. As a result, these two DNA fragments were successfully concentrated up to 60 fold at different location in a single paper-channel. The device would be a promising platform for point-of-care device due to an economic fabrication, the easy extraction of concentrated sample and an easy disposability.

  7. Flow injection analysis with tubular membrane ion-selective electrode and coated wires for buspirone hydrochloride.

    Science.gov (United States)

    Abdel-Ghani, Nour; Issa, Yousry; Shoukry, Adel; Ahmed, Howayda

    2007-01-01

    New Plastic membrane ion-selective electrode for buspirone hydrochloride based on buspironium tetraphenylborate was prepared. The electrode exhibited mean slope of calibration graph of 58.4 mV per decade of BusCl concentration at 25 degrees C. The electrode can be used within the concentration range 6.3 x 10(-5) - 10(-2) M BusCl at a pH range of 2.5-7.0. The standard electrode potentials were determined at different temperatures and used to calculate the isothermal temperature coefficient of the electrode, amounting to 0.00056 V degrees C(-1). The electrode showed a very good selectivity for BusCl with respect to a number of inorganic cations, sugars and amino acids. The electrode was applied to the potentiometric determination of the buspirone ion and its pharmaceutical preparation under batch and flow injection conditions. Also, buspirone was determined by conductimetric titrations. Graphite rod, copper and silver coated wire electrodes were prepared and characterized as sensors for the drug under investigation.

  8. Probing the selective separation of potassium ion from sodium ion with cyclopentadienyl anion as receptor: a computational study.

    Science.gov (United States)

    Desai, Mittal L; Si, Mrinal Kanti; Lo, Rabindranath; Ganguly, Bishwajit

    2015-08-01

    A systematic computational study has been carried out using post-Hartree-Fock and density functional theory methods on half sandwich (M-Cp), sandwich (Cp-M-Cp), inversed sandwich (M-Cp-M), and multi-decker chain complexes of alkali metal ions (Na(+), and K(+)). The binding affinity of cyclopentadienyl anion (Cp) with K(+) and Na(+) ions has been studied in half sandwich, sandwich, inversed sandwich, and multi-decker chain complexes. These complexes have been examined in the aqueous phase. The calculated results show that Cp anion can preferentially bind with Na(+) ion over K(+) ion in aqueous phase. The results obtained from DFT calculations have been compared with the crystal structures of Cp-Na and Cp-K complexes. The Bader's atoms in molecule (AIM) analysis were performed to characterize the non-covalent cation-π interactions in the Cp-M complexes. The calculated electron density at cage critical point indicates the strength of the Cp-M complexes. Energy decomposition analysis (EDA) has also been performed to investigate the origins of these interactions. The electrostatic interaction contributes significantly to the total interaction energy in Cp-M complexes. The relative stability difference of cyclopentadienyl anion (Cp) with K(+) and Na(+) ions in aqueous phase can be exploited for the separations from mixture such as sea bittern. The lower stability of K-Cp complex can induce to precipitate the K(+) ions more easily than the corresponding Na(+) ions. Graphical Abstract Potassium ion from sodium ion with cyclopentadienyl anion as receptor.

  9. Analysis of high-altitude planetary ion velocity space distributions detected by the Ion Mass Analyzer aboard Mars Express

    Science.gov (United States)

    Johnson, B. C.; Liemohn, M. W.; Fraenz, M.; Curry, S.; Mitchell, D. L.

    2012-12-01

    We present observations of planetary ion velocity space distributions from the Ion Mass Analyzer (IMA) onboard Mars Express (MEX). The magnetometer data from Mars Global Surveyor is used to obtain a rough estimate of the interplanetary magnetic field (IMF) orientation. Characteristic features of the velocity space distributions will be examined and discussed for orbits aligned with the convective electric field and those in the Mars terminator plane. This study will focus on the high (keV) energy ions, as well as the relative importance of a high-altitude magnetosheath source of escaping planetary ions. Furthermore, this paper will examine various methods for converting the IMA detector counts to species-specific fluxes. After mimicking the methods previously used by researchers, we apply each of these methods of species extraction to data collected during the same time intervals. We discuss the implications for planetary ion motion around Mars, using the details of the velocity space observations to better understand the solar wind interaction with Mars. Comparisons to virtual detections using a test particle simulation will also provide insight into ion origins and trajectories.

  10. Ion-ion coincidence imaging at high event rate using an in-vacuum pixel detector

    Science.gov (United States)

    Long, Jingming; Furch, Federico J.; Durá, Judith; Tremsin, Anton S.; Vallerga, John; Schulz, Claus Peter; Rouzée, Arnaud; Vrakking, Marc J. J.

    2017-07-01

    A new ion-ion coincidence imaging spectrometer based on a pixelated complementary metal-oxide-semiconductor detector has been developed for the investigation of molecular ionization and fragmentation processes in strong laser fields. Used as a part of a velocity map imaging spectrometer, the detection system is comprised of a set of microchannel plates and a Timepix detector. A fast time-to-digital converter (TDC) is used to enhance the ion time-of-flight resolution by correlating timestamps registered separately by the Timepix detector and the TDC. In addition, sub-pixel spatial resolution (principle experiment on strong field dissociative double ionization of carbon dioxide molecules (CO2), using a 400 kHz repetition rate laser system. The experimental results demonstrate that the spectrometer can detect multiple ions in coincidence, making it a valuable tool for studying the fragmentation dynamics of molecules in strong laser fields.

  11. Ion implantation of highly corrosive electrolyte battery components

    Science.gov (United States)

    Muller, Rolf H.; Zhang, Shengtao

    1997-01-01

    A method of producing corrosion resistant electrodes and other surfaces in corrosive batteries using ion implantation is described. Solid electrically conductive material is used as the ion implantation source. Battery electrode grids, especially anode grids, can be produced with greatly increased corrosion resistance for use in lead acid, molten salt, end sodium sulfur.

  12. Yolk-shell structured Sb@C anodes for high energy Na-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Song, Junhua; Yan, Pengfei; Luo, Langli; Qi, Xingguo; Rong, Xiaohui; Zheng, Jianming; Xiao, Biwei; Feng, Shuo; Wang, Chongmin; Hu, Yong-Sheng; Lin, Yuehe; Sprenkle, Vincent L.; Li, Xiaolin

    2017-10-01

    Despite great advances in sodium-ion battery developments, the search for high energy and stable anode materials remains a challenge. Alloy or conversion-typed anode materials are attractive candidates of high specific capacity and low voltage potential, yet their applications are hampered by the large volume expansion and hence poor electrochemical reversibility and fast capacity fade. Here, we use antimony (Sb) as an example to demonstrate the use of yolk-shell structured anodes for high energy Na-ion batteries. The Sb@C yolk-shell structure prepared by controlled reduction and selective removal of Sb2O3 from carbon coated Sb2O3 nanoparticles can accommodate the Sb swelling upon sodiation and improve the structural/electrical integrity against pulverization. It delivers a high specific capacity of ~554 mAh•g-1, good rate capability (315 mhA•g-1 at 10C rate) and long cyclability (92% capacity retention over 200 cycles). Full-cells of O3-Na0.9[Cu0.22Fe0.30Mn0.48]O2 cathodes and Sb@C-hard carbon composite anodes demonstrate a high specific energy of ~130 Wh•kg-1 (based on the total mass of cathode and anode) in the voltage range of 2.0-4.0 V, ~1.5 times energy of full-cells with similar design using hard carbon anodes.

  13. Enhanced selective removal of Cu(II) from aqueous solution by novel polyethylenimine-functionalized ion imprinted hydrogel: Behaviors and mechanisms

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Jingjing [State Key Laboratory of Pollutant Control and Resource Reuse, Nanjing 210023 (China); School of the Environment, Nanjing University, Nanjing 210023 (China); Li, Zhengkui, E-mail: zhkuili@nju.edu.cn [State Key Laboratory of Pollutant Control and Resource Reuse, Nanjing 210023 (China); School of the Environment, Nanjing University, Nanjing 210023 (China)

    2015-12-30

    Highlights: • A novel ion-imprinted poly(polyethylenimine/hydroxyethyl acrylate) hydrogel was synthesized. • The prepared hydrogel enhanced the selectivity of Cu(II) removal. • The material had high adsorption capacity and excellent regeneration property for copper. • The adsorption mechanism was the chelate interaction between functional groups and Cu(II) ions. - Abstract: A novel polyethylenimine-functionalized ion-imprinted hydrogel (Cu(II)-p(PEI/HEA)) was newly synthesized by {sup 60}Co-γ-induced polymerization for the selective removal of Cu(II) from aqueous solution. The adsorption performances including the adsorption capacity and selectivity of the novel hydrogel were much better than those of similar adsorbents reported. The hydrogel was characterized via scanning electron microscope, transmission electron microscopy, Fourier transform infrared spectra, thermal gravimetric analysis and X-ray photoelectron spectroscopy to determine the structure and mechanisms. The adsorption process was pH and temperature sensitive, better fitted to pseudo-second-order equation, and was Langmuir monolayer adsorption. The maximum adsorption capacity for Cu(II) was 40.00 mg/g. The selectivity coefficients of ion-imprinted hydrogel for Cu(II)/Pb(II), Cu(II)/Cd(II) and Cu(II)/Ni(II) were 55.09, 107.47 and 63.12, respectively, which were 3.93, 4.25 and 3.53 times greater than those of non-imprinted hydrogel, respectively. Moreover, the adsorption capacity of Cu(II)-p(PEI/HEA) could still keep more than 85% after four adsorption–desorption cycles. Because of such enhanced selective removal performance and excellent regeneration property, Cu(II)-p(PEI/HEA) is a promising adsorbent for the selective removal of copper ions from wastewater.

  14. Photoconductivity studies of the ferrocyanide ion under high pressure

    Energy Technology Data Exchange (ETDEWEB)

    Finston, M. I.

    1979-01-01

    The photoaquation of the ferrocyanide ion was studied using a high-pressure photoconductivity apparatus and a steady-state high-pressure mercury lamp. The first-order photocurrent rise-time could be related to the relative quantum efficiency of the photoaquation process, while the dark decay of the photocurrent yielded a relative value of the bimolecular rate-constant for the reverse reaction. Kinetic measurements were carried out on dilute solutions of potassium ferrocyanide in pure water, and in 20% ethanol. The photocurrent yield in aqueous solution was dependent upon secondary chemical equilibria which were sensitive to pressure in a predictable way. In ethanolic solution, the dependence of photocurrent yield on pressure followed the variation of the reciprocal solvent vicosity. In both aqueous and alcoholic solution, the photoaquation quantum efficiency decreased exponentially with pressure, as did the biomolecular rate-constant for the dark reaction in aqueous solution. The pressure dependence of the bimolecular rate-constant in the alcoholic solution indicated a diffusion-limited process. The pressure dependence of the photoaquation quantum yield, and of the bimolecular rate-constant in aqueous solution, was interpreted in terms of an activation volume model. The photoaquation data for both the aqueous and the alcoholic solutions agreed with a hypothetical mechanism whereby ligand-to-metal bond-breaking, and solvent-to-metal bond-formation, are effectively simultaneous. The results for the aqueous dark reaction strongly indicated breaking of the solvent-to-metal bond as the rate-limiting step.

  15. Fifth high-energy heavy-ion study

    Energy Technology Data Exchange (ETDEWEB)

    1981-10-01

    This was the fifth of a continuing series of summer studies held at LBL to discuss high energy heavy ion collisions. Recently, a similar meeting has been held on alternate years at GSI (Darmstadt); and, in 1979, we held a meeting at LBL exclusively devoted to ultra-relativistic nuclear collisions. Two new features distinguish this study from earlier meetings in the series. First, the energy range for discussion was broadened by including collisions from about 20 MeV/nucleon to the highest available in the cosmic radiation. The lower range, particularly below 100 MeV/nucleon, will be under intense study in the near future with machines such as the upgraded Bevalac, Michigan State University Superconducting Cyclotron, GANIL in France, and the SC at CERN. Recently, the high energy collision regime has been expanded by the successful operation of the CERN ISR with alpha particles. Second, in addition to an extensive program of invited talks, we decided for the first time to actively solicit contributions. Forty-seven individual items from the conference were prepared separately for the data base. (GHT)

  16. Zinc Metal-Organic Framework for Selective Detection and Differentiation of Fe(III) and Cr(VI) Ions in Aqueous Solution.

    Science.gov (United States)

    Lv, Rui; Li, Hui; Su, Jian; Fu, Xin; Yang, Boyi; Gu, Wen; Liu, Xin

    2017-10-16

    A new luminescent Zn(II)-based metal-organic framework (MOF), [Zn 2 (TPOM)(NDC) 2 ]·3.5H 2 O (Zn-MOF; TPOM = tetrakis(4-pyridyloxymethylene)methane and H 2 ndc = 2,6-naphthalenedicarboxylic acid), was successfully synthesized by a hydrothermal reaction. The MOF exhibits excellent luminescence emission, and it can detect Fe(III) and Cr(VI) ions with high selectivity, well antiinterference performance, and short response time. In addition, Zn-MOF was selected as a parent coordination compound to encapsulate Eu 3+ cations to obtain a Eu 3+ -incorporated sample (Eu 3+ @Zn-MOF). Subsequently, we explored the potential application of Eu 3+ @Zn-MOF as a probe for the selective sensing of Fe(III) and Cr(VI) ions, and it revealed that we could differentiate Fe(III) and Cr(VI) ions by the combination Zn-MOF and Eu 3+ @Zn-MOF. More importantly, it represents the first example of MOF-based luminescent sensors which can detect and differentiate Fe(III) and Cr(VI) ions selectively. And the possible sensing mechanism was discussed in detail.

  17. High density plasma reactive ion etching of Ru thin films using non-corrosive gas mixture

    Energy Technology Data Exchange (ETDEWEB)

    Hwang, Su Min; Garay, Adrian Adalberto; Lee, Wan In; Chung, Chee Won, E-mail: cwchung@inha.ac.kr

    2015-07-31

    Inductively coupled plasma reactive ion etching (ICPRIE) of Ru thin films patterned with TiN hard masks was investigated using a CH{sub 3}OH/Ar gas mixture. As the CH{sub 3}OH concentration in CH{sub 3}OH/Ar increased, the etch rates of Ru thin films and TiN hard masks decreased. However, the etch selectivity of Ru films on TiN hard masks increased and the etch slope of Ru film improved at 25% CH{sub 3}OH/Ar. With increasing ICP radiofrequency power and direct current bias voltage and decreasing process pressure, the etch rates of Ru films increased, and the etch profiles were enhanced without redeposition on the sidewall. Optical emission spectroscopy and X-ray photoelectron spectroscopy were employed to analyze the plasma and surface chemistry. Based on these results, Ru thin films were oxidized to RuO{sub 2} and RuO{sub 3} compounds that were removed by sputtering of ions and the etching of Ru thin films followed a physical sputtering with the assistance of chemical reaction. - Highlights: • Etching of Ru films in CH{sub 3}OH/Ar was investigated. • High selectivity and etch profile with high degree of anisotropy were obtained. • XPS analysis was examined to identify the etch chemistry. • During etching Ru was oxidized to RuO{sub 2} and RuO{sub 3} can be easily sputtered off.

  18. Characterization of a new ionophore-based ion-selective electrode for the potentiometric determination of creatinine in urine.

    Science.gov (United States)

    Guinovart, Tomàs; Hernández-Alonso, Daniel; Adriaenssens, Louis; Blondeau, Pascal; Rius, F Xavier; Ballester, Pablo; Andrade, Francisco J

    2017-01-15

    The optimization, analytical characterization and validation of a novel ion-selective electrode for the highly sensitive and selective determination of creatinine in urine is presented. A newly synthesized calix[4]pyrrole-based molecule is used as an ionophore for the enhanced recognition of creatininium cations. The calculation of the complex formation constants in the polymeric membrane with creatininium, potassium and sodium confirms the strong selective interactions between the ionophore and the target. The optimization of the potentiometric sensor presented here yields an outstanding analytical performance, with a linear range that spans from 1µM to 10mM and limit of detection of 10-6.2M. The calculation of the selectivity coefficients against most commonly found interferences also show significant improvements when compared to other sensors already reported. The performance of this novel sensor is tested by measuring creatinine in real urine samples (N=50) and comparing the values against the standard colorimetric approach (Jaffé's reaction). The results show that this sensor allows the fast and accurate determination of creatinine in real samples with minimal sample manipulation. Copyright © 2016 Elsevier B.V. All rights reserved.

  19. PACEM: a new concept for high avalanche-ion blocking

    Science.gov (United States)

    Veloso, J. F. C. A.; Amaro, F. D.; Azevedo, C. D. R.; dos Santos, J. M. F.; Breskin, A.; Lyashenko, A.; Chechik, R.

    2007-10-01

    We present the Photon-Assisted Cascaded Electron Multiplier (PACEM) as a potential alternative for ion back-flow suppression in gaseous cascade electron multipliers. Using a Micro Hole and Strip Plate-Gas Electron Multiplier (MHSP-GEM) configuration, the number of ions flowing back to the scintillation region is about 1.5 ions per primary electron at an optical gain of 6.5 and a drift field of 0.1 kV/cm, and about 10 ions per primary electron at an optical gain of 10 and a drift field of 0.5 kV/cm. These allow reaching ion back-flow values close to 10 -4 and 10 -5 at typical operation conditions of TPCs and GPMs, respectively.

  20. PACEM: a new concept for high avalanche-ion blocking

    Energy Technology Data Exchange (ETDEWEB)

    Veloso, J.F.C.A. [Departmento de Fisica, Universidade de Aveiro, P-3810-193 Aveiro (Portugal)], E-mail: joao.veloso@ua.pt; Amaro, F.D. [Departmento de Fisica, Universidade de Coimbra, P-3004-516 Coimbra (Portugal); Azevedo, C.D.R. [Departmento de Fisica, Universidade de Aveiro, P-3810-193 Aveiro (Portugal); Santos, J.M.F. dos [Departmento de Fisica, Universidade de Coimbra, P-3004-516 Coimbra (Portugal); Breskin, A.; Lyashenko, A.; Chechik, R. [Department of Particle Physics, The Weizmann Institute of Science, 76100 Rehovot (Israel)

    2007-10-21

    We present the Photon-Assisted Cascaded Electron Multiplier (PACEM) as a potential alternative for ion back-flow suppression in gaseous cascade electron multipliers. Using a Micro Hole and Strip Plate-Gas Electron Multiplier (MHSP-GEM) configuration, the number of ions flowing back to the scintillation region is about 1.5 ions per primary electron at an optical gain of 6.5 and a drift field of 0.1 kV/cm, and about 10 ions per primary electron at an optical gain of 10 and a drift field of 0.5 kV/cm. These allow reaching ion back-flow values close to 10{sup -4} and 10{sup -5} at typical operation conditions of TPCs and GPMs, respectively.

  1. Fabrication of coated graphite electrode for the selective determination of europium (III) ions.

    Science.gov (United States)

    Upadhyay, Anjali; Singh, Ashok Kumar; Bandi, Koteswara Rao; Jain, A K

    2013-10-15

    Preliminary complexation study showed that two ligands (ionophores) (2-((2-phenyl-2-(pyridin-2-yl)hydazono)methyl)pyridine) [L1], (2-((2-phenyl-2-(pyridin-2-yl)hydazono) methyl)phenol) [L2] can act as europium selective electrode. Europium selective coated graphite electrodes (CGE) were prepared by using ligands [L1] and [L2] and their potentiometric characteristics were determined. Membranes having different compositions of poly(vinylchloride) (PVC), the different plasticizers, anionic additives and ionophores were coated onto the graphite surface. The potential response measurements showed that the best performance was exhibited by the proposed CGE. This electrode had the widest working concentration range, Nernstian slope and fast response times of 10s. The selectivity studies showed that this electrode have higher selectivity towards Eu(3+) over a large number of cations. Furthermore, the electrode generated constant potentials in the pH range 2.7-9.0. This electrode can be used to quantify europium in soil, binary mixtures and also used as an indicator electrode in the potentiometric titration of Eu(3+) with EDTA. The proposed electrode was also successfully applied to the determination of fluoride ions in real samples. © 2013 Elsevier B.V. All rights reserved.

  2. Preparation of cold Mg{sup +}ion clouds for sympathetic cooling of highly charged ions at SPECTRAP

    Energy Technology Data Exchange (ETDEWEB)

    Cazan, Radu Mircea

    2012-02-15

    The bound electrons in hydrogen-like or lithium-like heavy ions experience extremely strong electric and magnetic fields in the surrounding of the nucleus. Laser spectroscopy of the ground-state hyperfine splitting in the lead region provides a sensitive tool to test strong-field quantum electro dynamics (QED), especially in the magnetic sector. Previous measurements on hydrogen-like systems performed in an electron-beam ion trap (EBIT) or at the experimental storage ring (ESR) were experimentally limited in accuracy due to statistics, the large Doppler broadening and the ion energy. The full potential of the QED test can only be exploited if measurements for hydrogen- and lithium-like ions are performed with accuracy improved by 2-3 orders of magnitude. Therefore, the new Penning trap setup SPECTRAP - dedicated for laser spectroscopy on trapped and cooled highly charged ions - is currently commissioned at GSI Darmstadt. Heavy highly charged ions will be delivered to this trap by the HITRAP facility in the future. SPECTRAP is a cylindrical Penning trap with axial access for external ion injection and radial optical access mounted inside a cold-bore superconducting Helmholtz-type split-coil magnet. To reach the targeted accuracy in laser spectroscopy, an efficient and fast cooling process for the highly charged ions must be employed. This can be realized by sympathetic cooling with a cloud of laser-cooled light ions. Within this thesis work, a laser system and an ion source for the production of such a {sup 24}Mg{sup +} ion cloud was developed and commissioned at SPECTRAP. An all-solid-state laser system for the generation of 279.6 nm light was designed and built. It consists of a fiber laser at 1118.5 nm followed by frequency quadrupling using two successive second-harmonic generation stages with actively stabilized ring resonators and nonlinear crystals. The laser system can deliver more than 15 mW of UV laser power under optimal conditions and requires little

  3. Experimental characterization of the Hitrap Cooler trap with highly charged ions.

    OpenAIRE

    Fedotova, Svetlana

    2013-01-01

    The HITRAP (Highly charged Ions TRAP)facility is being set up and commissioned at GSI, Darmstadt. It will provide heavy, highly charged ions at low velocities to high-precision atomic physics experiments. Within this work the Cooler trap- the key element of the HITRAP facility was tested. The Cooler trap was assembled, aligned, and commissioned in trapping experiments with ions from off-line sources.The work performed within the scope of this thesis provided the baseline for further operation...

  4. SOURCES OF COPPER IONS AND SELECTED METHODS OF THEIR REMOVAL FROM WASTEWATER FROM THE PRINTED CIRCUITS BOARD PRODUCTION

    Directory of Open Access Journals (Sweden)

    Maciej Thomas

    2014-10-01

    Full Text Available This paper presents the issues related to the presence and removal of copper compounds from industrial effluents with including wastewater from plants involved in the production of printed circuit boards. Characterized the toxicological properties of selected copper compounds, described the applicable technological processes, sources of copper ions in the effluents and selected methods for their removal.

  5. Highly nitrogen-doped carbon capsules: scalable preparation and high-performance applications in fuel cells and lithium ion batteries.

    Science.gov (United States)

    Hu, Chuangang; Xiao, Ying; Zhao, Yang; Chen, Nan; Zhang, Zhipan; Cao, Minhua; Qu, Liangti

    2013-04-07

    Highly nitrogen-doped carbon capsules (hN-CCs) have been successfully prepared by using inexpensive melamine and glyoxal as precursors via solvothermal reaction and carbonization. With a great promise for large scale production, the hN-CCs, having large surface area and high-level nitrogen content (N/C atomic ration of ca. 13%), possess superior crossover resistance, selective activity and catalytic stability towards oxygen reduction reaction for fuel cells in alkaline medium. As a new anode material in lithium-ion battery, hN-CCs also exhibit excellent cycle performance and high rate capacity with a reversible capacity of as high as 1046 mA h g(-1) at a current density of 50 mA g(-1) after 50 cycles. These features make the hN-CCs developed in this study promising as suitable substitutes for the expensive noble metal catalysts in the next generation alkaline fuel cells, and as advanced electrode materials in lithium-ion batteries.

  6. Simultaneous Counter-Ion Co-Deposition a Technique Enabling Matrix Isolation Spectroscopy Studies Using Low-Energy Beams of Mass-Selected Ions

    Science.gov (United States)

    Ludwig, Ryan M.; Moore, David T.

    2014-06-01

    Matrix isolation spectroscopy was first developed in Pimentel's group during the 1950's to facilitate spectroscopic studies of transient species. Cryogenic matrices of condensed rare gases provide an inert chemical environment with facile energy dissipation and are transparent at all wavelengths longer than vacuum UV, making them ideal for studying labile and reactive species such as radicals, weakly bound complexes, and ions. Since frozen rare gases are poor electrolytes, studies of ions require near-equal populations of anions and cations in order to stabilize the number densities required for spectroscopic experiments. Many techniques for generation of ions for using in matrix isolation studies satisfy this criterion intrinsically, however when ion beams generated in external sources are deposited, the counter-ions typically arise via secondary processes that are at best loosely controlled. It has long been recognized that it would be desirable to stabilize deposition of mass-selected ions generated in an external source using simultaneous co-deposition of a beam of counter-ions, however previous attempts to achieve this have been reported as unsuccessful. The Moore group at Lehigh has demonstrated successful experiments of this type, using mass-selected anions generated from a metal cluster source, co-deposited with a balanced current of cations generated in a separate electron ionization source. This talk will focus on the details of the technique, and present some results from proof-of-concept studies on anionic copper carbonyl complexes formed in argon matrices following co-deposition of Cu- with Ar+ or Kr+. Funding support from NSF CAREER Award CHE-0955637 is gratefully acknowledged. Whittle et al., J. Chem. Phys. 22, p.1943 (1954); Becker et al., J. Chem. Phys. 25, p.224 (1956). Godbout et al., J. Chem. Phys. 96, p.2892 (1996). Sabo et al., Appl. Spectrosc. 45, p. 535 (1991).

  7. Achieving High Resolution Ion Mobility Separations Using Traveling Waves in Compact Multiturn Structures for Lossless Ion Manipulations.

    Science.gov (United States)

    Hamid, Ahmed M; Garimella, Sandilya V B; Ibrahim, Yehia M; Deng, Liulin; Zheng, Xueyun; Webb, Ian K; Anderson, Gordon A; Prost, Spencer A; Norheim, Randolph V; Tolmachev, Aleksey V; Baker, Erin S; Smith, Richard D

    2016-09-20

    We report on ion mobility (IM) separations achievable using traveling waves (TW) in a Structures for Lossless Ion Manipulations (SLIM) module having a 44 cm path length and 16 90° turns. The performance of the TW-SLIM module was evaluated for ion transmission and IM separations with different RF, TW parameters, and SLIM surface gaps in conjunction with mass spectrometry. In this work, TWs were created by the transient and dynamic application of DC potentials. The module demonstrated highly robust performance and, even with 16 closely spaced turns, achieving IM resolution performance and ion transmission comparable to a similar straight path module. We found an IM peak capacity of ∼31 and peak generation rate of 780 s(-1) for TW speeds of ∼80 m/s using the current multi-turn TW-SLIM module. The separations achieved for isomers of peptides and tetrasaccharides were found to be comparable to those from a ∼0.9-m drift tube-based IM-MS platform operated at the same pressure (4 Torr). The combined attributes of flexible design, low voltage requirements and lossless ion transmission through multiple turns for the present TW-SLIM module provides a basis for SLIM devices capable of achieving much greater IM resolution via greatly extended ion path lengths and using compact serpentine designs.

  8. Ion optics and beam dynamics optimization at the HESR storage ring for the SPARC experiments with highly charged heavy ions

    Energy Technology Data Exchange (ETDEWEB)

    Kovalenko, Oleksandr

    2015-06-24

    The High-Energy Storage Ring (HESR) is a part of an upcoming International Facility for Antiproton and Ion Research (FAIR) at GSI in Darmstadt. A key part of a scientific program, along with antiproton physics, will be physics with highly-charged heavy ions. Phase-space cooled beams together with fixed internal target will provide an excellent environment for storage ring experiments at the HESR for the SPARC collaboration. Until recently, however, the existing ion optical lattice for the HESR was designed only for the experiments with antiproton beams. The thesis presents a new ion optical mode developed specifically for the operation of the HESR with highly charged heavy ions. The presence of the errors, such as beam momentum spread, magnetic field impurities or magnets misalignments, leads to disruption of beam dynamics: exciting of resonant motion and loss of beam stability. Within the paper, these effects are investigated with the help of numerical codes for particle accelerator design and simulation MAD-X and MIRKO. A number of correction techniques are applied to minimize the nonlinear impact on the beam dynamics and improve the experimental conditions. The application of the analytical and numerical tools is demonstrated in the experiment with uranium U{sup 90+} beam at the existing storage ring ESR, GSI.

  9. Treasure Na-ion anode from trash coke by adept electrolyte selection

    Science.gov (United States)

    Cabello, Marta; Chyrka, Taras; Klee, Rafael; Aragón, María J.; Bai, Xue; Lavela, Pedro; Vasylchenko, Gennadiy M.; Alcántara, Ricardo; Tirado, José L.; Ortiz, Gregorio F.

    2017-04-01

    Converting 'trash' waste residua to active functional materials 'treasure' with high added value is being regarded as a promising way to achieve the sustainable energy demands. Carbonaceous materials cannot insert sodium except when graphite co-intercalates solvents such as diglyme. Here, we show that petroleum coke and shale coke annealed at different temperatures can also insert sodium by reversible intercalation phenomena in a diglyme-based electrolyte. The structural and morphological studies will reveal significant differences justifying their distinct electrochemical behavior. Galvanostatic tests exhibit a flat plateau at about 0.7 V ascribable to the reversible reaction. At the end of the discharge, a Stage-I ternary intercalation compound is detected. Two diglyme molecules are co-intercalated per alkali ion, as evidenced by 1-D Patterson diagrams, FTIR and TGA analyses. The full sodium-ion cell made with P-2500/NaPF6(diglyme)/Na3V2(PO4)3 delivered an initial reversible capacity of 75 mA h g-1 at C rate and an average potential of 2.7 V. Thus, the full cell provides an energy density of 202 W h kg-1. This sodium-ion system can be considered a promising power source that encourages the potential use of low-cost energy storage systems.

  10. Ion-Selective Electrode for the Determination of Iron(III in Vitamin Formulations

    Directory of Open Access Journals (Sweden)

    Teixeira Marcos Fernando de S.

    1998-01-01

    Full Text Available A coated graphite-epoxy ion-selective electrode for iron(III, based on the ion-pair formed between [Fe(citrate2]3- and the tricaprylylmethylammonium cation (Aliquat 336 in a poly(vinylchloride (PVC matrix has been constructed. A thin membrane film of this ion-pair, dibutylphthalate (DBPh in PVC was deposited directly onto a Perspex® tube, which contained a graphite-epoxy conductor substrate. The coating solution was prepared by dissolving 30% (w/w of PVC in 10 mL of tetrahydrofuran following addition of 65% (w/w DBPh and 5% (w/w of the ionic pair. The effect of pH, citrate concentration and some cations on the electrode response has been investigated. The E(mV vs. log [Fe(citrate2]3- electrode response was linear for iron(III concentration from 1.0 x 10-3 mol/L to 1.0 x 10-1 mol/L in 1.0 mol/L citrate medium, with a slope of 19.3 ± 0.5 mV/decade and a useful lifetime of at least six months (more than 800 determinations for each polymeric membrane used. The detection limit was 7.5 x 10-4 mol/L and the relative standard deviation was less than 3% for a solution containing 5.0 x 10-3 mol/L of iron(III (n = 10. The application of this electrode for iron(III determination in samples of vitamin formulations is described. The results obtained with this procedure are in close agreement with those obtained using AA spectrophotometry (r = 0.9999.

  11. Synthesis, spectral characterization, thermal investigation and electrochemical evaluation of benzilbis(carbohydrazone as Cd(II ion selective electrode

    Directory of Open Access Journals (Sweden)

    Sulekh Chandra

    2017-02-01

    Full Text Available Benzil bis(carbohydrazone (BBC has been synthesized and structurally characterized on the basis of IR, 1H NMR, mass, UV spectra and thermogravimetric analyses. BBC has been analysed electrochemically and explored as new N, N Schiff base. It plays the role of an excellent ion carrier in the construction of cadmium(II ion selective membrane sensor. This sensor shows very good selectivity and sensitivity towards cadmium ion over a wide variety of cations, including alkali, alkaline earth, transition and heavy metal ions. The response mechanism was discussed in the view of UV-spectroscopy and Electrochemical impedance spectroscopy (EIS. The proposed sensor was successfully used for the determination of cadmium in different chocolate samples.

  12. Selective Improvement of NO2 Gas Sensing Behavior in SnO2 Nanowires by Ion-Beam Irradiation.

    Science.gov (United States)

    Kwon, Yong Jung; Kang, Sung Yong; Wu, Ping; Peng, Yuan; Kim, Sang Sub; Kim, Hyoun Woo

    2016-06-01

    We irradiated SnO2 nanowires with He ions (45 MeV) with different ion fluences. Structure and morphology of the SnO2 nanowires did not undergo noticeable changes upon ion-beam irradiation. Chemical equilibrium in SnO2/gas systems was calculated from thermodynamic principles, which were used to study the sensing selectivity of the tested gases, demonstrating the selective sensitivity of the SnO2 surface to NO2 gas. Being different from other gases, including H2, ethanol, acetone, SO2, and NH3, the sensor response to NO2 gas significantly increases as the ion fluence increases, showing a maximum under an ion fluence of 1 × 10(16) ions/cm(2). Photoluminescence analysis shows that the relative intensity of the peak at 2.1 eV to the peak at 2.5 eV increases upon ion-beam irradiation, suggesting that structural defects and/or tin interstitials have been generated. X-ray photoelectron spectroscopy indicated that the ionic ratio of Sn(2+/)Sn(4+) increases by the ion-beam irradiation, supporting the formation of surface Sn interstitials. Using thermodynamic calculations, we explained the observed selective sensing behavior. A molecular level model was also established for the adsorption of NO2 on ion-irradiated SnO2 (110) surfaces. We propose that the adsorption of NO2-related species is considerably enhanced by the generation of surface defects that are comprised of Sn interstitials.

  13. A System For High Flexibility Entangling Gates With Trapped Ions

    Science.gov (United States)

    Milne, Alistair; Edmunds, Claire; Mavadia, Sandeep; Green, Todd; Biercuk, Michael

    Trapped ion qubits may be entangled via coupling to shared modes of motion using spin-dependent forces generated by optical fields. Residual qubit-motional coupling at the conclusion of the entangling operation is the dominant source of infidelity in this type of gate. For synchronously entangling increasing numbers of ions, longer gate times are required to minimise this residual coupling. We present a scheme that enables the state of each qubit to be simultaneously dec