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Sample records for adsorbed oxygen ions

  1. Oxygen ion conducting materials

    DOEpatents

    Vaughey, John; Krumpelt, Michael; Wang, Xiaoping; Carter, J. David

    2005-07-12

    An oxygen ion conducting ceramic oxide that has applications in industry including fuel cells, oxygen pumps, oxygen sensors, and separation membranes. The material is based on the idea that substituting a dopant into the host perovskite lattice of (La,Sr)MnO.sub.3 that prefers a coordination number lower than 6 will induce oxygen ion vacancies to form in the lattice. Because the oxygen ion conductivity of (La,Sr)MnO.sub.3 is low over a very large temperature range, the material exhibits a high overpotential when used. The inclusion of oxygen vacancies into the lattice by doping the material has been found to maintain the desirable properties of (La,Sr)MnO.sub.3, while significantly decreasing the experimentally observed overpotential.

  2. Oxygen ion conducting materials

    DOEpatents

    Carter, J. David; Wang, Xiaoping; Vaughey, John; Krumpelt, Michael

    2004-11-23

    An oxygen ion conducting ceramic oxide that has applications in industry including fuel cells, oxygen pumps, oxygen sensors, and separation membranes. The material is based on the idea that substituting a dopant into the host perovskite lattice of (La,Sr)MnO.sub.3 that prefers a coordination number lower than 6 will induce oxygen ion vacancies to form in the lattice. Because the oxygen ion conductivity of (La,Sr)MnO.sub.3 is low over a very large temperature range, the material exhibits a high overpotential when used. The inclusion of oxygen vacancies into the lattice by doping the material has been found to maintain the desirable properties of (La,Sr)MnO.sub.3, while significantly decreasing the experimentally observed overpotential.

  3. Oxygen ion conducting materials

    DOEpatents

    Vaughey, John; Krumpelt, Michael; Wang, Xiaoping; Carter, J. David

    2003-01-01

    An oxygen ion conducting ceramic oxide that has applications in industry including fuel cells, oxygen pumps, oxygen sensors, and separation membranes. The material is based on the idea that substituting a dopant into the host perovskite lattice of (La,Sr)MnO.sub.3 that prefers a coordination number lower than 6 will induce oxygen ion vacancies to form in the lattice. Because the oxygen ion conductivity of (La,Sr)MnO.sub.3 is low over a very large temperature range, the material exhibits a high overpotential when used. The inclusion of oxygen vacancies into the lattice by doping the material has been found to maintain the desirable properties of (La,Sr)MnO.sub.3, while significantly decreasing the experimentally observed overpotential.

  4. Mimetite Formation from Goethite-Adsorbed Ions.

    PubMed

    Kleszczewska-Zębala, Anna; Manecki, Maciej; Bajda, Tomasz; Rakovan, John; Borkiewicz, Olaf J

    2016-06-01

    Bioavailability of arsenic in contaminated soils and wastes can be reduced to insignificant levels by precipitation of mimetite Pb5(AsO4)3Cl. The objective of this study is to elucidate mechanisms of the reaction between solution containing lead ions and arsenates adsorbed on synthetic goethite (AsO4-goethite), or arsenate ions in the solution and goethite saturated with adsorbed Pb (Pb-goethite). These reactions, in the presence of Cl, result in rapid crystallization of mimetite. Formation of mimetite is faster than desorption of AsO4 but slower than desorption of Pb from the goethite surface. Slow desorption of arsenates from AsO4-goethite results in heterogeneous precipitation and formation of mimetite incrustation on goethite crystals. Desorption of lead from Pb-goethite is at least as fast as diffusion and advection of AsO4 and Cl in suspension allowing for homogeneous crystallization of mimetite in intergranular solution. Therefore, the mechanism of nucleation is primarily driven by the kinetics of constituent supply to the saturation front, rather than by the thermodynamics of nucleation. The products of the reactions are well documented using microscopy methods such as scanning electron microscopy, electron backscattered diffraction, X-ray diffraction, and Fourier transform infrared spectroscopy.

  5. Adsorption of lead ions on composite biopolymer adsorbent

    SciTech Connect

    Seki, Hideshi; Suzuki, Akira

    1996-04-01

    A fundamental study about the application of biopolymers to the recovery of lead from dilute solution was carried out. A membranous composite biopolymer adsorbent containing two kind of biopolymers, alginic acid (AA) and humic acid (HA), was prepared. HA, which has high solubility in water, was almost completely immobilized in the adsorbent by a combination of calcium alginate gel and activated carbon powder. A general model for complexation between divalent metal ions and acidic sites on biopolymers was applied to explain the adsorption mechanism of lead on the adsorbent (HA-M). The results showed that the complexation constants and the complexation capacities of lead-AA and lead-HA systems were scarcely influenced by immobilization.

  6. Selective removal of copper and lead ions by diethylenetriamine-functionalized adsorbent: behaviors and mechanisms.

    PubMed

    Liu, Changkun; Bai, Renbi; San Ly, Quan

    2008-03-01

    The selective removal of copper and lead ions from aqueous solutions by diethylenetriamine (DETA)-functionalized polymeric adsorbent was investigated. The adsorbent was prepared by amination of the micro-beads synthesized from glycidyl methacrylate and trimethylolpropane trimethacrylate co-polymerization (denoted as P-DETA). In the single metal species system (only copper or lead ions present), P-DETA was found to adsorb copper ions or lead ions significantly (with a slightly higher adsorption uptake capacity for lead ions than copper ions). However, P-DETA displayed an excellent selectivity in the adsorption of copper ions over lead ions in the binary metal species system (with both copper and lead ions present). It was also found that initially (or previously) adsorbed lead ions on P-DETA were displaced, even completely, by subsequently adsorbed copper ions from the solution but the case was not vice versa. The greater electronegativity of copper ions than lead ions was identified as the major factor that caused P-DETA to selectively adsorb copper ions over lead ions during competitive adsorption in the binary metal species system. It was speculated that the displacement of already adsorbed lead ions on P-DETA by subsequently adsorbed copper ions was through an adjacent attachment and repulsion mechanism. P-DETA has been shown to have the potential to be used as an effective adsorbent for the removal as well as selective recovery of heavy metal ions in water or wastewater treatment.

  7. Titanate-based adsorbents for radioactive ions entrapment from water.

    PubMed

    Yang, Dongjiang; Liu, Hongwei; Zheng, Zhanfeng; Sarina, Sarina; Zhu, Huaiyong

    2013-03-21

    This feature article reviews some titanate-based adsorbents for the removal of radioactive wastes (cations and anions) from water. At the beginning, we discuss the development of the conventional ion-exchangeable titanate powders for the entrapment of radioactive cations, such as crystalline silicotitanate (CST), monosodium titanate (MST), peroxotitanate (PT). Then, we specially emphasize the recent progress in the uptake of radioactive ions by one-dimensional (1D) sodium titanate nanofibers and nanotubes, which includes the synthesis and phase transformation of the 1D nanomaterials, adsorption ability (capacity, selectivity, kinetics, etc.) of radioactive cations and anions, and the structural evolution during the adsorption process.

  8. Composite oxygen ion transport element

    DOEpatents

    Chen, Jack C.; Besecker, Charles J.; Chen, Hancun; Robinson, Earil T.

    2007-06-12

    A composite oxygen ion transport element that has a layered structure formed by a dense layer to transport oxygen ions and electrons and a porous support layer to provide mechanical support. The dense layer can be formed of a mixture of a mixed conductor, an ionic conductor, and a metal. The porous support layer can be fabricated from an oxide dispersion strengthened metal, a metal-reinforced intermetallic alloy, a boron-doped Mo.sub.5Si.sub.3-based intermetallic alloy or combinations thereof. The support layer can be provided with a network of non-interconnected pores and each of said pores communicates between opposite surfaces of said support layer. Such a support layer can be advantageously employed to reduce diffusion resistance in any type of element, including those using a different material makeup than that outlined above.

  9. Fast removal of copper ions from aqueous solution using an eco-friendly fibrous adsorbent.

    PubMed

    Niu, Yaolan; Ying, Diwen; Li, Kan; Wang, Yalin; Jia, Jinping

    2016-10-01

    Functional PET fiber (PET-AA-CS) was prepared by oxygen-plasma pretreatment and grafting of acrylic acid (AA) and low-molecular-weight chitosan (LMCS) on the polyethylene glycol terephthalate (PET) substrate. This adsorbent was targeted for quick removal of metal ion in river pollutions with an easy recycling of the fiber after emergency processing. The fabricated PET-AA-CS was characterized by the scanning electron microscope (SEM), contact angle, fourier transform infrared (FTIR) spectra and X-ray photoelectron spectroscopy (XPS) to look into its morphology, surface functional groups, and adsorption mechanism of copper ions from the aqueous solution. The overall adsorption process of copper ions on the PET-AA-CS was pH-dependent with an optimal pH value of 5.0, at which a maximum capacity of 68.97 mg g(-1) was obtained. The result of fitting also shows that adsorption process follows the Langmuir isotherm and pseudo-second-order model. Moreover, the material shows good stability during 5 cycles of adsorption and desorption, and also shows no significant effect of co-existing ions including Ca(2+), Mg(2+), K(+), Cl(-), and et al. In general, PET-AA-CS developed in this study shows significant benefit of eco-friend and cost-efficiency for fast removal of copper ions in potential river metal pollutions comparing with traditional adsorbents.

  10. Fast removal of copper ions from aqueous solution using an eco-friendly fibrous adsorbent.

    PubMed

    Niu, Yaolan; Ying, Diwen; Li, Kan; Wang, Yalin; Jia, Jinping

    2016-10-01

    Functional PET fiber (PET-AA-CS) was prepared by oxygen-plasma pretreatment and grafting of acrylic acid (AA) and low-molecular-weight chitosan (LMCS) on the polyethylene glycol terephthalate (PET) substrate. This adsorbent was targeted for quick removal of metal ion in river pollutions with an easy recycling of the fiber after emergency processing. The fabricated PET-AA-CS was characterized by the scanning electron microscope (SEM), contact angle, fourier transform infrared (FTIR) spectra and X-ray photoelectron spectroscopy (XPS) to look into its morphology, surface functional groups, and adsorption mechanism of copper ions from the aqueous solution. The overall adsorption process of copper ions on the PET-AA-CS was pH-dependent with an optimal pH value of 5.0, at which a maximum capacity of 68.97 mg g(-1) was obtained. The result of fitting also shows that adsorption process follows the Langmuir isotherm and pseudo-second-order model. Moreover, the material shows good stability during 5 cycles of adsorption and desorption, and also shows no significant effect of co-existing ions including Ca(2+), Mg(2+), K(+), Cl(-), and et al. In general, PET-AA-CS developed in this study shows significant benefit of eco-friend and cost-efficiency for fast removal of copper ions in potential river metal pollutions comparing with traditional adsorbents. PMID:27470942

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

    PubMed

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

    2014-02-01

    A polyaniline-based composite cation-exchange material was synthesized by way of sol-gel method and studied to explore its analytical and environmental applications. It was characterized by using instrumental analyses [Fourier transform infrared (spectrometer), X-ray, thermogravimetric analysis/differential thermal analysis, standard electron microscopy, and transmission electron microscopy]. Physicochemical studies, such as ion-exchange capacity, pH titrations, and chemical stability, along with effect of eluent concentration and elution, were also performed to exploit the ion-exchange capabilities. pH titration studies showed that the material presents monofunctional strong cation-exchange behavior. This nanocomposite material is semicrystalline in nature and exhibits improved thermal and chemical stability. The partition coefficient studies of different metal ions in the material were performed in demineralised water and different surfactant media, and it was found to be selective for Pb(II) and Hg(II) ions. To exploit the usefulness of the material as an adsorbent, some important quantitative binary separations of metal ions were performed on polyaniline Zr(IV) molybdophosphate columns. This composite cation exchanger can be applied for the treatment of polluted water to remove heavy metals. PMID:24292693

  12. Oxygen ion-beam microlithography

    DOEpatents

    Tsuo, Y.S.

    1991-08-20

    A method of providing and developing a resist on a substrate for constructing integrated circuit (IC) chips includes the following steps: of depositing a thin film of amorphous silicon or hydrogenated amorphous silicon on the substrate and exposing portions of the amorphous silicon to low-energy oxygen ion beams to oxidize the amorphous silicon at those selected portions. The nonoxidized portions are then removed by etching with RF-excited hydrogen plasma. Components of the IC chip can then be constructed through the removed portions of the resist. The entire process can be performed in an in-line vacuum production system having several vacuum chambers. Nitrogen or carbon ion beams can also be used. 5 figures.

  13. Oxygen ion-beam microlithography

    DOEpatents

    Tsuo, Y. Simon

    1991-01-01

    A method of providing and developing a resist on a substrate for constructing integrated circuit (IC) chips includes the following steps: of depositing a thin film of amorphous silicon or hydrogenated amorphous silicon on the substrate and exposing portions of the amorphous silicon to low-energy oxygen ion beams to oxidize the amorphous silicon at those selected portions. The nonoxidized portions are then removed by etching with RF-excited hydrogen plasma. Components of the IC chip can then be constructed through the removed portions of the resist. The entire process can be performed in an in-line vacuum production system having several vacuum chambers. Nitrogen or carbon ion beams can also be used.

  14. Oxygen release from nanobubbles adsorbed on hydrophobic particles

    NASA Astrophysics Data System (ADS)

    Zhao, Wanchen; Hu, Xiutao; Duan, Juan; Liu, Ting; Liu, Minghuan; Dong, Yaming

    2014-07-01

    On the hydrophobic particles, the carrying capacity of nano/microbubbles and the quantity of oxygen released in the hypoxic environment are still unknown while the bubbles blow out. This is very important to the biological and medical systems. Here, an experiment was designed and the change of the dissolved oxygen in a solution was monitored. The results indicated that the concentrations of dissolved oxygen in hypoxic environment changed dramatically, especially when the ultrasound vibration was applied. Furthermore, the amount of oxygen release also implied the quantity dependence of nano/microbubbles on the sizes and the hydrophobicity of the particles.

  15. Active site densities, oxygen activation and adsorbed reactive oxygen in alcohol activation on npAu catalysts.

    PubMed

    Wang, Lu-Cun; Friend, C M; Fushimi, Rebecca; Madix, Robert J

    2016-07-01

    The activation of molecular O2 as well as the reactivity of adsorbed oxygen species is of central importance in aerobic selective oxidation chemistry on Au-based catalysts. Herein, we address the issue of O2 activation on unsupported nanoporous gold (npAu) catalysts by applying a transient pressure technique, a temporal analysis of products (TAP) reactor, to measure the saturation coverage of atomic oxygen, its collisional dissociation probability, the activation barrier for O2 dissociation, and the facility with which adsorbed O species activate methanol, the initial step in the catalytic cycle of esterification. The results from these experiments indicate that molecular O2 dissociation is associated with surface silver, that the density of reactive sites is quite low, that adsorbed oxygen atoms do not spill over from the sites of activation onto the surrounding surface, and that methanol reacts quite facilely with the adsorbed oxygen atoms. In addition, the O species from O2 dissociation exhibits reactivity for the selective oxidation of methanol but not for CO. The TAP experiments also revealed that the surface of the npAu catalyst is saturated with adsorbed O under steady state reaction conditions, at least for the pulse reaction. PMID:27376884

  16. Effect of adsorbed chlorine and oxygen on shear strength of iron and copper junctions

    NASA Technical Reports Server (NTRS)

    Wheeler, D. R.

    1975-01-01

    Static friction experiments were performed in ultrahigh vacuum at room temperature on copper, iron, and steel contacts selectively contaminated with oxygen and chlorine in submonolayer amounts. The concentration of the adsorbates was determined with Auger electron spectroscopy and was measured relative to the saturation concentration of oxygen on iron (concentration 1.0). The coefficient of static friction decreased with increasing adsorbate concentration. It was independent of the metal and the adsorbate. The results compared satisfactorily with an extension of the junction growth theory to heterogeneous interfaces. The reduction in interfacial shear strength was measured by the ratio sub a/sub m where sub a is the shear strength of the interface with an adsorbate concentration of 1.0, and sub m is the strength of the clean metal interface. This ratio was 0.835 + or - 0.012 for all the systems tested.

  17. Effect of adsorbed chlorine and oxygen on the shear strength of iron and copper junctions

    NASA Technical Reports Server (NTRS)

    Wheeler, D. R.

    1976-01-01

    Static-friction experiments were performed in ultrahigh vacuum at room temperature on copper, iron, and steel contacts selectively contaminated with oxygen and chlorine in submonolayer amounts. The concentration of the adsorbates was determined with Auger electron spectroscopy and was measured relative to the saturation concentration of oxygen on iron (concentration, 1.0). The coefficient of static friction decreased with increasing adsorbate concentration; however, it was independent of the type of metal and the adsorbate species. The results compared satisfactorily with an extension of the junction growth theory to heterogeneous interfaces. The reduction in interfacial shear strength was measured by the ratio of the shear strength of the interface with an adsorbate concentration of 1.0 and the strength of the clean metal interface. This ratio was about 0.835 for all the systems tested.

  18. Mixed oxygen ion/electron-conducting ceramics for oxygen separation

    SciTech Connect

    Stevenson, J.W.; Armstrong, T.R.; Armstrong, B.L.

    1996-08-01

    Mixed oxygen ion and electron-conducting ceramics are unique materials that can passively separate high purity oxygen from air. Oxygen ions move through a fully dense ceramic in response to an oxygen concentration gradient, charge-compensated by an electron flux in the opposite direction. Compositions in the system La{sub 1{minus}x}M{sub x}Co{sub 1{minus}y{minus}z}Fe{sub y}N{sub z}O{sub 3{minus}{delta}}, perovskites where M=Sr, Ca, and Ba, and N=Mn, Ni, Cu, Ti, and Al, have been prepared and their electrical, oxygen permeation, oxygen vacancy equilibria, and catalytic properties evaluated. Tubular forms, disks, and asymmetric membrane structures, a thin dense layer on a porous support of the same composition, have been fabricated for testing purposes. In an oxygen partial gradient, the passive oxygen flux through fully dense structures was highly dependent on composition. An increase in oxygen permeation with increased temperature is attributed to both enhanced oxygen vacancy mobility and higher vacancy populations. Highly acceptor-doped compositions resulted in oxygen ion mobilities more than an order of magnitude higher than yttria-stabilized zirconia. The mixed conducting ceramics have been utilized in a membrane reactor configuration to upgrade methane to ethane and ethylene. Conditions were established to balance selectivity and throughput in a catalytic membrane reactor constructed from mixed conducting ceramics.

  19. Oxygen Photochemistry on TiO2(110): Recyclable, Photoactive Oxygen Produced by Annealing Adsorbed O2

    SciTech Connect

    Petrik, Nikolay G.; Kimmel, Gregory A.

    2011-11-03

    Photon-stimulated reactions between chemisorbed and physisorbed oxygen on TiO2(110) are investigated. Experiments using O2 isotopologues show that UV irradiation results in the exchange of atoms between chemisorbed and physisorbed oxygen. Annealing chemisorbed oxygen to {approx}350 K maximizes these exchange reactions, while dissociatively adsorbing oxygen on TiO2(110) at 300 - 350 K does not lead to reactions with physisorbed O2. After annealing to 350 K, the exchange products photodesorb in the plane perpendicular to the bridge-bonded oxygen rows at an angle of 45{sup o}. In contrast, the chemisorbed O2 photodesorbs normal to the surface. Remarkably, the chemisorbed species is stable under multiple cycles of UV irradiation with physisorbed O2. The active atoms in the chemisorbed species can be changed from 18O to 16O and then back to 18O via the exchange reactions. The results show that annealing oxygen adsorbed on TiO2(110) to {approx}350 K produces a stable chemical species with interesting photochemical properties. Possible forms for the photoactive species include O2 adsorbed in a bridging oxygen vacancy or tetraoxygen.

  20. EFFECT OF DISSOLVED OXYGEN ON PHENOLS BREAKTHROUGH FROM GAC ADSORBERS

    EPA Science Inventory

    This study demonstrates that molecular oxygen plays an important role in the adsorption of organic compounds from water by activated carbon. It was determined that the adsorptive capacity of granular activated carbon (GAC) for o-cresol can increase by almost 200% as a result of...

  1. Impact of co-adsorbed oxygen on crotonaldehyde adsorption over gold nanoclusters: a computational study.

    PubMed

    Zeinalipour-Yazdi, Constantinos D; Willock, David J; Machado, Andreia; Wilson, Karen; Lee, Adam F

    2014-06-21

    Crotonaldehyde (2-butenal) adsorption over gold sub-nanometer particles, and the influence of co-adsorbed oxygen, has been systematically investigated by computational methods. Using density functional theory, the adsorption energetics of crotonaldehyde on bare and oxidised gold clusters (Au13, d = 0.8 nm) were determined as a function of oxygen coverage and coordination geometry. At low oxygen coverage, sites are available for which crotonaldehyde adsorption is enhanced relative to bare Au clusters by 10 kJ mol(-1). At higher oxygen coverage, crotonaldehyde is forced to adsorb in close proximity to oxygen weakening adsorption by up to 60 kJ mol(-1) relative to bare Au. Bonding geometries, density of states plots and Bader analysis, are used to elucidate crotonaldehyde bonding to gold nanoparticles in terms of partial electron transfer from Au to crotonaldehyde, and note that donation to gold from crotonaldehyde also becomes significant following metal oxidation. At high oxygen coverage we find that all molecular adsorption sites have a neighbouring, destabilising, oxygen adatom so that despite enhanced donation, crotonaldehyde adsorption is always weakened by steric interactions. For a larger cluster (Au38, d = 1.1 nm) crotonaldehyde adsorption is destabilized in this way even at a low oxygen coverage. These findings provide a quantitative framework to underpin the experimentally observed influence of oxygen on the selective oxidation of crotyl alcohol to crotonaldehyde over gold and gold-palladium alloys.

  2. Fabricating electrospun cellulose nanofibre adsorbents for ion-exchange chromatography

    PubMed Central

    Dods, Stewart R.; Hardick, Oliver; Stevens, Bob; Bracewell, Daniel G.

    2015-01-01

    Protein separation is an integral step in biopharmaceutical manufacture with diffusion-limited packed bed chromatography remaining the default choice for industry. Rapid bind-elute separation using convective mass transfer media offers advantages in productivity by operating at high flowrates. Electrospun nanofibre adsorbents are a non-woven fibre matrix of high surface area and porosity previously investigated as a bioseparation medium. The effects of compression and bed layers, and subsequent heat treatment after electrospinning cellulose acetate nanofibres were investigated using diethylaminoethyl (DEAE) or carboxylate (COO) functionalisations. Transbed pressures were measured and compared by compression load, COO adsorbents were 30%, 70% and 90% higher than DEAE for compressions 1, 5 and 10 MPa, respectively, which was attributed to the swelling effect of hydrophilic COO groups. Dynamic binding capacities (DBCs) at 10% breakthrough were measured between 2000 and 12,000 CV/h (2 s and 0.3 s residence times) under normal binding conditions, and DBCs increased with reactant concentration from 4 to 12 mg BSA/mL for DEAE and from 10 to 21 mg lysozyme/mL for COO adsorbents. Comparing capacities of compression loads applied after electrospinning showed that the lowest load tested, 1 MPa, yielded the highest DBCs for DEAE and COO adsorbents at 20 mg BSA/mL and 27 mg lysozyme/mL, respectively. At 1 MPa, DBCs were the highest for the lowest flowrate tested but stabilised for flowrates above 2000 CV/h. For compression loads of 5 MPa and 10 MPa, adsorbents recorded lower DBCs than 1 MPa as a result of nanofibre packing and reduced surface area. Increasing the number of bed layers from 4 to 12 showed decreasing DBCs for both adsorbents. Tensile strengths were recorded to indicate the mechanical robustness of the adsorbent and be related to packing the nanofibre adsorbents in large scale configurations such as pleated cartridges. Compared with an

  3. Degradation Mechanisms in Oxygen Ion Conducting Materials

    NASA Astrophysics Data System (ADS)

    Lussier, Alexandre; Finsterbusch, Martin; Idzerda, Yves U.

    2010-03-01

    We have developed a testing apparatus to characterize degradation mechanisms in oxygen ion conducting materials, with an emphasis on Solid Oxide Fuel Cell (SOFC) materials. While chemical potentials drive currents in SOFCs, we utilize a simple electrical potential to drive oxygen ionic currents through materials and interfaces. We can additionally adjust the temperature and gaseous environment of our experiment, enabling us to identify and characterize degradation mechanisms and their causes. Early performance results confirm multiple SOFC cathode degradation mechanisms driven by both high temperatures and ion currents. In particular, cation inter-diffusion is prevalent at interfaces such as those between La(0.6)Sr(0.4)Co(0.2)Fe(0.8)O(3) and Ga-doped CeO(2) resulting in an interfacial structure which is increasingly resistant to subsequent oxygen ion flow. By isolating and understanding various degradation mechanisms we can more effectively address those mechanisms to improve long term ion conducting material performance.

  4. Oxygen ions observed near Saturn's A ring.

    PubMed

    Waite, J H; Cravens, T E; Ip, W-H; Kasprzak, W T; Luhmann, J G; McNutt, R L; Niemann, H B; Yelle, R V; Mueller-Wodarg, I; Ledvina, S A; Scherer, S

    2005-02-25

    Ions were detected in the vicinity of Saturn's A ring by the Ion and Neutral Mass Spectrometer (INMS) instrument onboard the Cassini Orbiter during the spacecraft's passage over the rings. The INMS saw signatures of molecular and atomic oxygen ions and of protons, thus demonstrating the existence of an ionosphere associated with the A ring. A likely explanation for these ions is photoionization by solar ultraviolet radiation of neutral O2 molecules associated with a tenuous ring atmosphere. INMS neutral measurements made during the ring encounter are dominated by a background signal.

  5. Oxygen Isotope Fractionation Effects in Soil Water via Cations Adsorbed to High-CEC Clays

    NASA Astrophysics Data System (ADS)

    Oerter, E.; Finstad, K.; Schaefer, J.; Goldsmith, G. R.; Dawson, T. E.; Amundson, R.

    2012-12-01

    adsorbed). Water isotope data generated from direct equilibration of magnesium-saturated montmorillonite was depleted by 2‰ and 4‰ (δ18O) for the 25% and 5% water content samples, respectively. This revealed preferential adsorption of 18O isotopologues within hydrations shells around the clay/ion complex. In contrast, potassium-saturated montmorillonite showed an isotope effect in opposite direction and with a smaller magnitude (~1‰ enrichment of free water in δ18O for both the high and low water content experiments). Experiments to evaluate conditions more similar to those found in nature are also underway using dilute solutions of Mg, K and Ca. Linking isotope hydrology with the growing understanding of mineral-water reaction has several immediate impacts. First, direct CO2/soil water equilibration (either in lab or field) is a growing method for determining the oxygen isotope composition of soil water. Results thus far indicate these measurements reveal the isotope ratios of a special portion of the total soil water. Second, one of the key controls on the oxygen isotope composition of atmospheric CO2 is exchange with the soil water, which is largely assumed to follow precipitation inputs. A few per mil shift in the value of this equilibration has potentially large impacts on rates of the biotic fluxes which are of primary interest in these calculations.

  6. Chitosan membrane adsorber for low concentration copper ion removal.

    PubMed

    Wang, Xiaomin; Li, Yanxiang; Li, Haigang; Yang, Chuanfang

    2016-08-01

    Thin chitosan membranes with symmetric and interconnected pore structure were prepared using silica as porogen, and their physical properties including pore structure, pore size distribution, porosity and water affinity were analyzed. The membrane showed a maximum Cu(II) adsorption capacity of 87.5mg/g in static adsorption, and the adsorption fitted pseudo-second order kinetics and Toth adsorption isotherm. The membranes were then stacked in layers as an adsorber to remove small concentration Cu(II) from water dynamically. At feed concentration of 5mg/L, the adsorber could retain Cu(II) effectively when its thickness reached over 200μm, and the performance was further improved by using more membranes layers. Within a certain limit, the adsorber showed a 'flow-independent' loading behavior, an indication of fast mass transfer inside the membrane. The adsorption process was correlated well with bed depth service time (BDST) model, Thomas model and Yoon and Nelson model, and the adsorber was also found to be regenerable and re-usable. PMID:27112875

  7. Atomic and molecular oxygen adsorbed on (111) transition metal surfaces: Cu and Ni

    SciTech Connect

    López-Moreno, S.; Romero, A. H.

    2015-04-21

    Density functional theory is used to investigate the reaction of oxygen with clean copper and nickel [111]-surfaces. We study several alternative adsorption sites for atomic and molecular oxygen on both surfaces. The minimal energy geometries and adsorption energies are in good agreement with previous theoretical studies and experimental data. From all considered adsorption sites, we found a new O{sub 2} molecular precursor with two possible dissociation paths on the Cu(111) surface. Cross barrier energies for the molecular oxygen dissociation have been calculated by using the climbing image nudge elastic band method, and direct comparison with experimental results is performed. Finally, the structural changes and adsorption energies of oxygen adsorbed on surface when there is a vacancy nearby the adsorption site are also considered.

  8. Magnetized Mars: Spatial distribution of oxygen ions

    NASA Astrophysics Data System (ADS)

    Kallio, Esa; Barabash, Stas

    2012-02-01

    We have studied the spatial distribution of oxygen ions near Mars assuming that the planet had a weak intrinsic magnetic field sometimes in the past. The study has been performed by using a global self-consistent numerical hybrid model HYB-Mars by simulating four magnetization cases when the strength of the dipole magnetic field on surface at the magnetic equator was 0 nT, 10 nT, 30 nT and 60 nT. In all cases the upstream solar wind conditions were assumed to be present day nominal values. Two different regions were found: (1) a closed magnetic field line region where the density of oxygen ions was high and the ion velocity small and (2) an open magnetic region near the magnetic poles where both the density and the velocity of planetary oxygen ions were high. The former region has similarities with Earth's plasmasphere and the latter with Earth's magnetic cusps. The size of the closed magnetic field region increases with increasing dipolar field. The oxygen ions originating from the ionosphere were found to escape easily along the magnetic field from the magnetic cusps but become trapped within the closed magnetic field line region. The model used does not include a self-consistent ionosphere but it is interesting to note that the total loss rate had a local maximum at a small non-zero value of the magnetic dipole field (10 nT).

  9. Removal of heavy metal ions from wastewater by chemically modified plant wastes as adsorbents: a review.

    PubMed

    Wan Ngah, W S; Hanafiah, M A K M

    2008-07-01

    The application of low-cost adsorbents obtained from plant wastes as a replacement for costly conventional methods of removing heavy metal ions from wastewater has been reviewed. It is well known that cellulosic waste materials can be obtained and employed as cheap adsorbents and their performance to remove heavy metal ions can be affected upon chemical treatment. In general, chemically modified plant wastes exhibit higher adsorption capacities than unmodified forms. Numerous chemicals have been used for modifications which include mineral and organic acids, bases, oxidizing agent, organic compounds, etc. In this review, an extensive list of plant wastes as adsorbents including rice husks, spent grain, sawdust, sugarcane bagasse, fruit wastes, weeds and others has been compiled. Some of the treated adsorbents show good adsorption capacities for Cd, Cu, Pb, Zn and Ni.

  10. Aptamer selection for fishing of palladium ion using graphene oxide-adsorbed nanoparticles.

    PubMed

    Cho, Yea Seul; Lee, Eun Jeong; Lee, Gwan-Ho; Hah, Sang Soo

    2015-12-01

    A new aptamer selection method using graphene oxide (GO)-adsorbed nanoparticles (GO-adsorbed NPs) was employed for specific fishing of palladium ion. High affinity ssDNA aptamers were isolated through 13 rounds of selection and the capacity of the selected DNA aptamers for palladium ion uptake was measured, clarifying that DNA01 exhibits the highest affinity to palladium ion with a dissociation constant (Kd) of 4.60±1.17 μM. In addition, binding ability of DNA01 to palladium ion was verified against other metal ions, such as Li(+), Cs(+), Mg(2+), and Pt(2+). Results of the present study suggest that future modification of DNA01 may improve palladium ion-binding ability, leading to economic recovery of palladium from water solution.

  11. Phosphorylated cellulose triacetate-silica composite adsorbent for recovery of heavy metal ion.

    PubMed

    Srivastava, Niharika; Thakur, Amit K; Shahi, Vinod K

    2016-01-20

    Phosphorylated cellulose triacetate (CTA)/silica composite adsorbent was prepared by acid catalyzed sol-gel method using an inorganic precursor (3-aminopropyl triethoxysilane (APTEOS)). Reported composite adsorbent showed comparatively high adsorption capacity for Ni(II) in compare with different heavy metal ions (Cu(2+), Ni(2+), Cd(2+) and Pb(2+)). For Ni(II) adsorption, effect of time, temperature, pH, adsorbent dose and adsorbate concentration were investigated; different kinetic models were also evaluated. Thermodynamic parameters such as ΔG°, ΔH° and ΔS° were also estimated and equilibrium adsorption obeyed Langmuir and Freundlich isotherms. Developed adsorbent exhibited about 78.8% Ni(II) adsorption at pH: 6 and a suitable candidate for the removal of Ni(II) ions from wastewater. Further, about 65.5% recovery of adsorbed Ni(II) using EDTA solution was demonstrated, which suggested effective recycling of the functionalized beads would enable it to be used in the treatment of contaminated water in industry. PMID:26572476

  12. Adsorbent for metal ions and method of making and using

    DOEpatents

    White, Lloyd R.; Lundquist, Susan H.

    2000-01-01

    A method comprises the step of spray-drying a solution or slurry comprising (alkali metal or ammonium) (metal) hexacyanoferrate particles in a liquid, to provide monodisperse, substantially spherical particles in a yield of at least 70 percent of theoretical yield and having a particle size in the range of 1 to 500 micrometers, said particles being active towards Cs ions. The particles, which can be of a single salt or a combination of salts, can be used free flowing, in columns or beds, or entrapped in a nonwoven, fibrous web or matrix or a cast porous membrane, to selectively remove Cs ions from aqueous solutions.

  13. Adsorbent for metal ions and method of making and using

    DOEpatents

    White, L.R.; Lundquist, S.H.

    1999-08-10

    A method comprises the step of spray-drying a solution or slurry comprising (alkali metal or ammonium) (metal) hexacyanoferrate particles in a liquid, to provide monodisperse, substantially spherical particles in a yield of at least 70 percent of theoretical yield and having a particle size in the range of 1 to 500 micrometers, said particles being active towards Cs ions. The particles, which can be of a single salt or a combination of salts, can be used free flowing, in columns or beds, or entrapped in a nonwoven, fibrous web or matrix or a cast porous membrane, to selectively remove Cs ions from aqueous solutions. 2 figs.

  14. Adsorbent for metal ions and method of making and using

    DOEpatents

    White, Lloyd R.; Lundquist, Susan H.

    1999-01-01

    A method comprises the step of spray-drying a solution or slurry comprising (alkali metal or ammonium) (metal) hexacyanoferrate particles in a liquid, to provide monodisperse, substantially spherical particles in a yield of at least 70 percent of theoretical yield and having a particle size in the range of 1 to 500 micrometers, said particles being active towards Cs ions. The particles, which can be of a single salt or a combination of salts, can be used free flowing, in columns or beds, or entrapped in a nonwoven, fibrous web or matrix or a cast porous membrane, to selectively remove Cs ions from aqueous solutions.

  15. Negative thermal ion mass spectrometry of oxygen in phosphates

    NASA Astrophysics Data System (ADS)

    Holmden, C.; Papanastassiou, D. A.; Wasserburg, G. J.

    1997-06-01

    A novel technique for the precise measurement of oxygen isotopes by negative thermal ion mass spectrometry (NTIMS) is presented. The technique is ideally suited to the analysis of oxygen isotopes in phosphates which form intense P03 ion beams. Since P is monoisotopic, the mass spectrum for P0 3- at 79, 80, and 81 corresponds to 1660, 170, and 180. Natural and synthetic phosphates are converted and loaded on the mass spectrometer filament as Ag 3PO 4 precipitated directly from ammoniacal solution. To lower the work function of the filament, BaCl, is added in a 1:1 molar ratio of PO 4:Ba. Using these procedures, Br - mass interference (at 79 and 81 amu) is eliminated for typical analyses. Experiments with 180-enriched water show less than 1 % O-exchange between sample PO 4 and adsorbed water, and there is no O-exchange with trace OZ present in the mass spectrometer source chamber. The ionization efficiency of PO 4, as P0 3- is >10% compared to 0.01% for both conventional dual inlet Gas Isotope Ratio Mass Spectrometry (GIRMS) and secondary ion mass spectrometry (SIMS). Therefore, NTIMS offers exceptional sensitivity enabling routine and precise oxygen isotope analysis of sub-microgram samples of PO 4, (<21 nmoles equivalent CO 2 gas) without need for lengthy chemical pre-treatment reproducibility of the sample. Overall external precision is ±1%c (2σ) for 18O/16 O and 170/15O with of instrumental isotope fractionation (calculated from 18O/16O of ±0.5%c amu -1. Small phosphate samples including single mineral grains from meteorites, or apatite microfossils, can be analyzed by this technique.

  16. Aluminum ion implantation under backfilling oxygen

    NASA Astrophysics Data System (ADS)

    Hausner, R. M.; Baumann, H.; Bethge, K.

    1996-06-01

    High dose ion implantation ( F ≥ 2 × 10 18 ions/cm 2) of 40 keV Al ions into stainless steel (AISI 321) under increased partial pressure of oxygen and oxygen compounds ( P ≥ 1 × 10 -8 hPa O 2, CO 2, N 2O) leads to the formation of a homogenous Al film on the sample surface due to a reduced self-sputtering yield of Al. The depth distribution of the implanted aluminum and the thickness of the Al film grown up on the sample were measured using the resonant nuclear reaction 27Al(p, γ) 28Si at 992 keV and by the (α, α) elastic backscattering at 3.05 MeV. The concentrations of the low- Z impurity oxygen and carbon were determined with the extremely strong resonances of the (α, α) elastic scattering under backward angles at 7.6 MeV for 16O and at 5.75 MeV for 12C. Furthermore the properties of the formed Al film were investigated by SEM, surface profile and microhardness measurements. The self-sputtering yield of Al was measured under normal vacuum conditions and under increased O 2 partial pressure, and the results were compared with the data obtained from calculations using the computer code T-DYN.

  17. Copper ions removal from water using functionalized carbon nanotubes–mullite composite as adsorbent

    SciTech Connect

    Tofighy, Maryam Ahmadzadeh; Mohammadi, Toraj

    2015-08-15

    Highlights: • CNTs–mullite composite was prepared via chemical vapor deposition (CVD) method. • The prepared composite was modified with concentrated nitric acid and chitosan. • The modified CNTs–mullite composites were used as novel adsorbents. • Copper ion removal from water by the prepared adsorbents was performed. • Langmuir and Freundlich isotherms and two kinetic models were applied to fit the experimental data. - Abstract: Carbon nanotubes–mullite composite was synthesized by direct growth of carbon nanotubes on mullite particles via chemical vapor deposition method using cyclohexanol and ferrocene as carbon precursor and catalyst, respectively. The carbon nanotubes–mullite composite was oxidized with concentrated nitric acid and functionalized with chitosan and then used as a novel adsorbent for copper ions removal from water. The results demonstrated that modification with concentrated nitric acid and chitosan improves copper ions adsorption capacity of the prepared composite, significantly. Langmuir and Freundlich isotherms and two kinetic models were applied to fit the experimental data. The carbon nanotubes growth on mullite particles to form the carbon nanotubes–mullite composite with further modification is an inherently safe approach for many promising environmental applications to avoid some concerns regarding environment, health and safety. It was found that the modified carbon nanotubes–mullite composite can be considered as an excellent adsorbent for copper ions removal from water.

  18. Sputtering and secondary ion emission properties of alkali metal films and adsorbed monolayers

    SciTech Connect

    Krauss, A R; Gruen, D M

    1980-01-01

    The secondary ion emission of alkali metal adsorbed monlayer and multilayer films has been studied. Profiling with sub-monolayer resolution has been performed by Auger, x-ray photoemission and secondary ion mass spectroscopy. Characteristic differences in the sputtering yields, and ion fraction have been observed which are associated with both the surface bonding properties and the mechanism leading to the formation of secondary ions. By sputtering with a negative bias applied to the sample, positive secondary ions are returned to the surface, resulting in a reduced sputter-induced erosion rate. Comparison with the results obtained with K and Li overlayers sputtered without sample bias provides an experimental value of both the total and secondary ion sputtering yields. The first and second monolayers can be readily identified and the first monolayer exhibits a lower sputtering yield and higher secondary ion fraction. This result is related to adsorption theory and measured values are compared with those obtained by thermal desorption measurements.

  19. Electronic Structures of Hydrogen and Oxygen Adsorbed Tungsten (3, 2, 0) and Tungsten (8, 7, 0) Surfaces

    NASA Astrophysics Data System (ADS)

    Bao, Zhuo; Bostwick, Aaron; Rotenberg, Eli; Kevan, Stephen

    2011-03-01

    The Valence band electronic structues of Hydrogen adsorbed and Oxygen adsorbed Tungsten stepped surfaces, Tungsten (3, 2, 0) and (8, 7, 0) surface are investigated using angular-resolved photoemission techniques and ab-initio electronic structure calculation methods. The band features of surface states at different Hydrogen and Oxygen coverages are experimentally distinguished by using photon-energy scanning method. Quasi-one- dimensional band features are found in the surface states with saturated Oxygen coverages of both stepped surfaces. The effects of adsorbate coverages on dimensionalities of surface electronic states are studied using high-resolution band mapping methods and ab-initio calculation methods. Thanks to Department of Energy for the financial supporting of this project.

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

    SciTech Connect

    Sun, G.; Shi, W.

    1998-04-01

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

  1. Adsorption of cadmium ions on oxygen surface sites in activated carbon

    SciTech Connect

    Jia, Y.F.; Thomas, K.M.

    2000-02-08

    Various types of oxygen functional groups were introduced onto the surface of coconut shell derived activated carbon by oxidation using nitric acid. Fourier-transform infrared spectroscopy (FTIR), temperature-programmed desorption (TPD), and selective neutralization were used to characterize the surface oxygen functional groups. The oxidized carbons were also heat treated to provide a suite of carbons where the oxygen functional groups of various thermal stabilities were varied progressively. The adsorption of cadmium ions was enhanced dramatically by oxidation of the carbon. The ratio of released protons to adsorbed cadmium ions on oxidized carbon was approximately 2, indicating cation exchange was involved in the process of adsorption. Na{sup +} exchange studies with the oxidized carbon gave a similar ratio. After heat treatment of the oxidized carbons to remove oxygen functional groups, the ratio of H{sup +} released to Cd{sup 2+} adsorbed and the adsorption capacity decreased significantly. Both reversible and irreversible processes were involved in cadmium ion adsorption with reversible adsorption having higher enthalpy. The irreversible adsorption resulted from cation exchange with carboxylic acid groups, whereas the reversible adsorption probably involved physisorption of the partially hydrated cadmium ion.

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

    PubMed

    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. PMID:27474562

  3. Fast vacancy-mediated oxygen ion incorporation across the ceria-gas electrochemical interface.

    PubMed

    Feng, Zhuoluo A; El Gabaly, Farid; Ye, Xiaofei; Shen, Zhi-Xun; Chueh, William C

    2014-07-09

    Electrochemical incorporation reactions are ubiquitous in energy storage and conversion devices based on mixed ionic and electronic conductors, such as lithium-ion batteries, solid-oxide fuel cells and water-splitting membranes. The two-way traffic of ions and electrons across the electrochemical interface, coupled with the bulk transport of mass and charge, has been challenging to understand. Here we report an investigation of the oxygen-ion incorporation pathway in CeO2-δ (ceria), one of the most recognized oxygen-deficient compounds, during hydrogen oxidation and water splitting. We probe the response of surface oxygen vacancies, electrons and adsorbates to the electrochemical polarization at the ceria-gas interface. We show that surface oxygen-ion transfer, mediated by oxygen vacancies, is fast. Furthermore, we infer that the electron transfer between cerium cations and hydroxyl ions is the rate-determining step. Our in operando observations reveal the precise roles of surface oxygen vacancy and electron defects in determining the rate of surface incorporation reactions.

  4. Reactions of atomic oxygen with the chlorate ion and the perchlorate ion

    NASA Astrophysics Data System (ADS)

    Anan'ev, Vladimir; Miklin, Mikhail; Kriger, Ludmila

    2014-06-01

    The reactions of the chlorate ion with atomic oxygen formed under photolysis of the nitrate ion introduced to potassium chlorate crystal by co-crystallization were studied by optical and infrared absorption spectroscopy. The perchlorate ion was found to form in solids as product of addition reaction of singlet atomic oxygen, formed under dissociation of the peroxynitrite ion - the product of isomerization of the excited nitrate ion. Triplet atomic oxygen does not react with the chlorate ion. The atomic oxygen formed under photolysis of the nitrate ion introduced to potassium perchlorate crystal by co-crystallization does not react with the perchlorate ion.

  5. The effect of oxygen during irradiation of silicon with low energy Cs{sup +} ions

    SciTech Connect

    Berghmans, B.; Vandervorst, W.

    2009-08-01

    The effect of oxygen flooding during ultralow energy SIMS depth profiling of silicon with Cs{sup +} primary ions is presented. New experimental data show the effective sputtering yield of silicon in the presence of oxygen, as well as the energy distribution of the secondary Si{sup -} ions. It is found that the component sputtering yield of Si is very sensitive to minute amounts of oxygen in the proximity of the sputtered surface. At these very low flooding pressures (in the 10{sup -9}-10{sup -8} mbar range), one cannot account for a full oxidation in the time frame of a typical measurement; it is concluded that in this particular case, which is technologically very relevant, small traces of oxygen will change the desorption characteristics of cesium as well as silicon. It shows that oxygen that is adsorbed to the silicon surface provides an attachment site for impinging cesium ions and thereby increases the retention capacity of cesium tremendously. Also, oxygen changes the secondary ion yield and can even promote the desorption of Si from the analysis surface.

  6. Facile preparation of hierarchical polyaniline-lignin composite with a reactive silver-ion adsorbability.

    PubMed

    He, Zhi-Wei; Lü, Qiu-Feng; Zhang, Jia-Yin

    2012-01-01

    A hierarchical polyaniline-lignin (PANI-EHL) composite was facilely prepared from aniline and enzymatic hydrolysis lignin in an aqueous solution of ammonia. The morphology, FTIR, UV-vis spectra, thermogravimetric analysis, and wide-angle X-ray diffraction analyses of the composite were systematically investigated. Furthermore, the sorption property of the PANI-EHL composite for silver ions in aqueous solution was studied via a static sorption technique. The result demonstrated that the PANI-EHL composite possessed a strongly reactive sorption characteristic for silver ions. Serrated silver threads with length up to 10 mm were obtained by using the PANI-EHL composite as a low-cost adsorbent. Moreover, the role of EHL and polyaniline in the PANI-EHL composite for silver ions sorption was investigated. The investigation indicated that the EHL unit could play a vital role in the chelation of silver ions, whereas the polyaniline unit played a leading role in redox sorption.

  7. The preparation of polyelectrolyte complexes carboxymethyl chitosan(CMC)-pectin by reflux method as a Pb (II) metal ion adsorbent

    NASA Astrophysics Data System (ADS)

    Hastuti, Budi; Mudasir, Siswanta, Dwi; Triyono

    2016-02-01

    Aim of this research is to synthesized a chemically stable polyelectrolyte complexs carboxymetyl chitosan CMC-pectin as Pb(II) ion adsorbent by reflux method. During synthesis process, the optimum mass ratio of CMC and pectin was pre-determined and the active groups of the CMC-pectin complex was characterized by using IR spectrofotometer. Finally, adsorption capacity of the adsorbent material for Pb (II) ions was studied under optimum condition, i.e. adsorbent mass, contact time, and pH. Result shows that CMC could be succesfully combined with pectin to produce CMC-pectin complex. The optimum mass ratio CMC: pectin to form the polyelectrolyte complexs CMC-pectin was 70% : 30%. The active groups identified in the CMC-pectin complex was a hydroxyl (OH) and carboxylate (-COOH) groups. The optimum conditions for Pb (II) ion absoprtion was 10 mg of the adsorbent mass, 75 min of contact time, and pH 5. This material can be effectively used as adsorbents for Pb (II) ions, where up to 91% Pb (II) metal ions was adsorbed from aqueous solution and the adsorption capacity of the adsorbent was 41.63 mg/g.

  8. Functionalized-MnO2/chitosan nanocomposites: A promising adsorbent for the removal of lead ions.

    PubMed

    Mallakpour, Shadpour; Madani, Maryam

    2016-08-20

    In the current study, the surface of alpha manganese dioxide nanorod (α-MnO2) functionalized with γ-aminopropyltriethoxysilane (APTS). The α-MnO2-APTS was used as filler for preparation of chitosan (CS) nanocomposites (NCs). The α-MnO2-APTS/CS NCs were crosslinked with different amount of glutaraldehyde (GA). The effects of the GA content on the morphology, thermal properties and adsorption of NC films were studied. The Fourier transform infrared (FT-IR) results verified the grafting of APTS onto α-MnO2. The amount of APTS grafted onto α-MnO2 was found to be 20wt% by thermo gravimetric analysis. Presented results also show that with increasing crosslinker agent concentration, the thermal stability of CS films were increased. The α-MnO2-APTS/CS NCs were tested and evaluated as a potential adsorbent for the removal of lead ions. The results showed that the adsorbent exhibited a favorable performance for the removal of lead ions. Therefore, α-MnO2-APTS/CS NCs could serve as promising adsorbents. PMID:27178908

  9. Nucleation and mobility model of Agn clusters adsorbed on perfect and oxygen vacancy MgO surfaces.

    PubMed

    Liu, Yongfei; Wang, Yan; Chen, Guangju

    2011-05-01

    The structures and energy properties for Ag(n) (n = 1-8) metal clusters adsorbed on the perfect and oxygen vacancy MgO surfaces have been studied by using the DFT/UB3LYP method with an embedded cluster model. The nucleation and mobility model for the Ag(n) (n = 1-8) clusters on the perfect and oxygen vacancy MgO(100) surfaces was investigated. The results show that the Ag atoms locate initially at the surface oxygen vacancy sites; then, with the growth of Ag cluster sizes, the large Ag clusters move possibly out of the vacancy sites by a rolling model, and diffuse on the MgO surface under a certain temperature condition. The relative energies needed for moving out of the oxygen vacancy region for the adsorbed Ag(n) clusters with the rolling model have been predicted. The even-odd oscillation behaviors for the cohesive energies, nucleation energies, first ionization potentials and HOMO-LUMO gaps of the adsorbed Ag(n) clusters with the variation of cluster sizes have also been discussed.

  10. Surface Modification of Polymer Substrates by Oxygen Ion Irradiation

    SciTech Connect

    Takaoka, G. H.; Ryuto, H.; Araki, R.; Yakushiji, T.

    2008-11-03

    Oxygen cluster ions and/or monomer ions were used for the sputtering and the surface modification of polymers such as polycarbonate (PC) and polyethylene terephthalate (PET). For the case of oxygen cluster ion irradiation, the sputtered depth increased with increase of the acceleration voltage, and the sputtering yield was much larger than that by the monomer ion irradiation. The sputtered particles represented the polymer structure, which indicated that the bond scission by the cluster ion irradiation resulted in an ejection of monomer molecule through the intermolecular collision. On the other hand, for the oxygen monomer ion irradiation, the implanted depth increased with increase of the acceleration voltage, and the bond scission occurred at the deep region through the binary collision with the high energetic ions. Therefore, the sputtering yield for the polymer surfaces decreased, and the sputtering effect became very small. Furthermore, the simultaneous use of oxygen cluster and monomer ions was more effective for oxidation of the PET surfaces rather than the monomer ion irradiation or the cluster ion irradiation. As a result, the contact angle measurement showed that the wettability of the PET surfaces irradiated by the simultaneous use of oxygen cluster and monomer ions was much enhanced.

  11. Probing the photochemistry of chemisorbed oxygen on TiO2(110) with Kr and other co-adsorbates.

    PubMed

    Petrik, Nikolay G; Kimmel, Greg A

    2014-02-14

    Weakly-bound atoms and molecules (Ar, Kr, Xe, CO, CH4, CO2, CH3OH, N2O, and N2) are used to probe the photochemical interactions of chemisorbed oxygen on rutile TiO2(110). Ultraviolet irradiation of chemisorbed oxygen co-adsorbed with the probe species leads to photon-stimulated desorption (PSD) of some of the probe species (e.g. Kr and CH4), but not others (e.g. CO2 and N2O). Without chemisorbed oxygen, the PSD yields of all the probe species are very low or not observed. Surprisingly, both chemisorbed O2 and oxygen adatoms, Oa, are photo-active for desorption of Kr and other weakly-bound species. To our knowledge, this is the first evidence for photo-activity of Oa on TiO2(110). The Kr PSD yield increases with increasing coverage of Kr and of chemisorbed oxygen. For Kr, the angular distribution of the photodesorbed atoms is approximately cosine. The Kr distribution is quite different from the angular distribution for the O2 PSD, which is sharply peaked along the surface normal. We propose that various forms of chemisorbed oxygen are excited by reactions with electrons and/or holes created in the TiO2 substrate by UV photon irradiation. The photo-excited oxygen collides with, and transfers energy to, neighboring co-adsorbed atoms or molecules. For co-adsorbates with a small enough binding energy to the substrate, desorption may result. The observed phenomenon provides a new tool for studying photochemical processes.

  12. Oxygen on Cu(100) a case of an adsorbate induced reconstruction

    NASA Astrophysics Data System (ADS)

    Wuttig, M.; Franchy, R.; Ibach, H.

    1989-04-01

    We show that at and above room temperature only a single long range ordered superstructure exists on Cu(100). This is the ( 2 × 2 2)R45° structure, which corresponds to a saturation coverage of θo = 0.48 ± 0.05. A well-ordered c(2 × 2) superstructure is not observed in the investigated range of adsorption temperatures ( Tads = 300-600 K). Above a critical oxygen coverage θc = 0.34 ±0.02 long range order starts to develop. The disordered adsorption region below θc = 0.34 is characterized by two different adsorption sites. One of these sites already is saturated at relatively low coverages (θ o ≅ 0.15). This site appears to corresponds to a local reconstruction with the neighbouring atoms of the adsorbate atom engaging in an intralayer contraction. Diffraction studies show a first order phase transition at θ c from the disordered phase to a phase with long range order. The long range ordered domains are larger than the coherence length of the EELS diffraction experiment already slightly above θ c. For the "Perfect" ( 2 ×2 2)R45° structure only a single fourfold coordinated adsorption site is occupied. The large number of total symmetric vibrations as well as the observed LEED pattern show that the substrate surface is reconstructed. An assignment of the observed vibrations allows us to determine the reconstruction pattern which is characterized by a local symmetry reduction. This lowering of symmetry might be the driving force of the reconstruction pointing towards a Peierls instability or a cooperative Jahn-Teller effect.

  13. A novel agricultural waste adsorbent for the removal of lead (II) ions from aqueous solutions.

    PubMed

    Ibrahim, M N Mohamad; Ngah, W S Wan; Norliyana, M S; Daud, W R Wan; Rafatullah, M; Sulaiman, O; Hashim, R

    2010-10-15

    The present study explores the ability of modified soda lignin (MSL) extracted from oil palm empty fruit bunches (EFB) in removing lead (II) ions from aqueous solutions. The effect of contact time, point zero charge (pH(pzc)) and pH of the solution, initial metal ion concentration and adsorbent dosage on the removal process were investigated. Furthermore, the MSL is characterized by SEM, XRF, FT-IR and surface area analysis. Equilibrium adsorption isotherms and kinetics were investigated. The experimental data were analyzed by the Langmuir, Freundlich and Temkin models of adsorption. The kinetic data obtained at different initial concentrations were analyzed using pseudo-first-order and pseudo-second-order models. The results provide strong evidence to support the hypothesis of adsorption mechanism.

  14. Free energy of electrical double layers: Entropy of adsorbed ions and the binding polynomial

    SciTech Connect

    Stigter, D.; Dill, K.A. )

    1989-09-07

    The authors adapt the method of binding polynomials to general problems of binding equilibria of ions to polybases, polyacids, and mixed polyelectrolytes, such as proteins and other colloids. For spherical particles with a smeared charge the interaction effects are taken into account using the Poisson-Boltzmann equation, which is shown to differ little from the Debye-Hueckel approximation under conditions met in most protein solutions. Examples are given of the salt dependence of pH titration equilibria. Binding polynomials produce an extra term in the free energy of the electrical double layer, which arises from the entropy of the adsorbed ions. The maximum term method applied to the binding polynominal yields an expression which is similar to that derived by the charging process of Chan and Mitchell. Applications to monolayers and to polyelectrolyte gels are also discussed.

  15. Column preconcentration and faas determination of heavy metal ions using Artemisia Siberi as an adsorbent.

    PubMed

    Mousavi, Hassan Zavvar; Derakhshankhah, Jalal

    2014-01-01

    A new column procedure for the determination of trace amounts of cadmium (II), lead (II), nickel (II), zinc (II), and copper (II), which combines flame atomic absorption spectrometry is described. These metals were sorbed on Artemisia siberi herb as an adsorbent at pH 4.0 and eluted with 3 mL of 1.5 M HNO3. The influences of analytical parameters including pH, flow rate, sample volume, type of eluent, and effect of diverse salts and cations on the recoveries of analyte ions were studied. The developed procedure provides preconcentration factors of about 117. LODs were 0.2 (Cd), 0.4 (Cu), 0.2 (Ni), 0.6 (Zn), and 1.4 (Pb) μg/L. The present method was successfully applied to the determination of the above-mentioned ions in water samples from Semnan, Iran. Recoveries greater than 95% and RSDs below 10% were obtained. PMID:25632447

  16. A novel starch-based adsorbent for removing toxic Hg(II) and Pb(II) ions from aqueous solution.

    PubMed

    Huang, Li; Xiao, Congming; Chen, Bingxia

    2011-08-30

    A novel effective starch-based adsorbent was prepared through two common reactions, which included the esterification of starch with excess maleic anhydride in the presence of pyridine and the cross-linking reaction of the obtained macromonomer with acrylic acid by using potassium persulphate as initiator. The percentage of carboxylic groups of the macromonomer ranged from 14% to 33.4%. The cross-linking degree of the adsorbent was tailored with the amount of acrylic acid which varied from 10wt% to 80wt%. Both Fourier transform infrared spectra and thermogravimetric analysis results verified the structure of the adsorbent. The maximum gel fraction and swelling ratio of the adsorbent were about 72% and 6.25, respectively, and they were able to be adjusted with the amount of monomers. The weight loss percentage of the adsorbent could reach 96.9% after immersing in the buffer solution that contained α-amylase for 14h. It was found that the adsorption capacities of the adsorbent for lead and mercury ions could be 123.2 and 131.2mg/g, respectively. In addition, the adsorbent was able to remove ca. 51-90% Pb(II) and Hg(II) ions that existed in the decoctions of four medicinal herbals. PMID:21724326

  17. Volumetric Interpretation of Protein Adsorption: Ion-Exchange Adsorbent Capacity, Protein pI, and Interaction Energetics

    PubMed Central

    Noh, Hyeran; Yohe, Stefan; Vogler, Erwin A.

    2008-01-01

    Adsorption of lysozyme (Lys), human serum albumin (HSA), and immunoglobulin G (IgG) to anion- and cation-exchange resins is dominated by electrostatic interactions between protein and adsorbent. The solution-depletion method of measuring adsorption shows, however, that these proteins do not irreversibly adsorb to ion-exchange surfaces, even when the charge disparity between adsorbent and protein inferred from protein pI is large. Net-positively-charged Lys (pI = 11) and net-negatively-charged HSA (pI = 5.5) adsorb so strongly to sulfopropyl sepharose (SP; a negatively-charged, strong cation exchange resin, −0.22 mmol/mL exchange capacity) that both resist displacement by net-neutral IgG (pI = 7.0) in simultaneous adsorption-competition experiments. By contrast, IgG readily displaces both Lys and HSA adsorbed either to quarternary-ammonium sepharose (Q; a positively-charged, strong anion exchanger, + 0.22 mmol/mL exchange capacity) or octadecyl sepharose (ODS, a neutral hydrophobic resin, 0 mmol/mL exchange capacity). Thus it is concluded that adsorption results do not sensibly correlate with protein pI and that pI is actually a rather poor predictor of affinity for ion-exchange surfaces. Adsorption of Lys, HSA, and IgG to ion-exchange resins from stagnant solution leads to adsorbed multi-layers, into-or-onto which IgG adsorbs in adsorption-competition experiments. Comparison of adsorption to ion-exchange resins and neutral ODS leads to the conclusion that the apparent standard free-energy-of-adsorption ΔGadso of Lys, HSA, and IgG is not large in comparison to thermal energy due to energy-compensating interactions between water, protein, and ion-exchange surfaces that leaves a small net ΔGadso. Thus water is found to control protein adsorption to a full range of substratum types spanning hydrophobic (poorly water wettable) surfaces, hydrophilic surfaces bearing relatively-weak Lewis acid/base functionalities that wet with (hydrogen bond to) water but do not

  18. Transmission of low energy (< 10 eV) oxygen ions through ultrathin xenon films

    NASA Astrophysics Data System (ADS)

    Sack, N. J.; Akbulut, M.; Madey, T. E.

    1994-05-01

    In studies of desorption induced by electronic transitions (DIET) such as electron or photon stimulated desorption, it is important to know whether the desorbing species originate solely from the outermost surface layer, or also from layers beneath the surface. In order to gain better understanding of the charge transfer, elastic scattering, and other inelastic processes involved in this issue, we are currently performing a series of experimental studies of the transmission of low energy ions (˜ 7 eV) through ultrathin films (submonolayer to multilayer) of condensed gases. Here we report on the first quantitative measurements of the yield, angle, and energy of oxygen ions after transmission through ultrathin films of xenon. In our novel approach, a focused 300 eV electron beam bombards a target at 25 K consisting of an oxidized tungsten (100) crystal with adsorbed overlayers of xenon. In the absence of the xenon, O + ions desorb in a sharp beam normal to the surface, as measured in a velocity and angle resolving ESDIAD apparatus (electron stimulated desorption ion angular distribution). When Xe layers are present, some oxygen ions penetrate several monolayers of xenon without significant change in energy and angle while others seem to be scattered by large-angle elastic scattering or to be attenuated from the O + beam. The work presented is the first experimental study of the depth of origin of desorbing ions in DIET processes.

  19. Oxygen ion-conducting dense ceramic

    DOEpatents

    Balachandran, Uthamalingam; Kleefisch, Mark S.; Kobylinski, Thaddeus P.; Morissette, Sherry L.; Pei, Shiyou

    1996-01-01

    Preparation, structure, and properties of mixed metal oxide compositions containing at least strontium, cobalt, iron and oxygen are described. The crystalline mixed metal oxide compositions of this invention have, for example, structure represented by Sr.sub..alpha. (Fe.sub.1-x Co.sub.x).sub..alpha.+.beta. O.sub..delta. where x is a number in a range from 0.01 to about 1, .alpha. is a number in a range from about 1 to about 4, .beta. is a number in a range upward from 0 to about 20, and .delta. is a number which renders the compound charge neutral, and wherein the composition has a non-perovskite structure. Use of the mixed metal oxides in dense ceramic membranes which exhibit oxygen ionic conductivity and selective oxygen separation, are described as well as their use in separation of oxygen from an oxygen-containing gaseous mixture.

  20. Oxygen ion-conducting dense ceramic

    DOEpatents

    Balachandran, Uthamalingam; Kleefisch, Mark S.; Kobylinski, Thaddeus P.; Morissette, Sherry L.; Pei, Shiyou

    1997-01-01

    Preparation, structure, and properties of mixed metal oxide compositions containing at least strontium, cobalt, iron and oxygen are described. The crystalline mixed metal oxide compositions of this invention have, for example, structure represented by Sr.sub..alpha. (Fe.sub.1-x Co.sub.x).sub..alpha.+.beta. O.sub..delta. where x is a number in a range from 0.01 to about 1, .alpha. is a number in a range from about 1 to about 4, .beta. is a number in a range upward from 0 to about 20, and .delta. is a number which renders the compound charge neutral, and wherein the composition has a non-perovskite structure. Use of the mixed metal oxides in dense ceramic membranes which exhibit oxygen ionic conductivity and selective oxygen separation, are described as well as their use in separation of oxygen from an oxygen-containing gaseous mixture.

  1. Determinants of protein elution rates from preparative ion-exchange adsorbents.

    PubMed

    Angelo, James M; Lenhoff, Abraham M

    2016-04-01

    The rate processes involved in elution in preparative chromatography can affect both peak resolution and hence selectivity as well as practical factors such as facility fit. These processes depend on the physical structure of the adsorbent particles, the amount of bound solute, the solution conditions for operation or some combination of these factors. Ion-exchange adsorbents modified with covalently attached or grafted polymer layers have become widely used in preparative chromatography. Their often easily accessible microstructures offer substantial binding capacities for biomolecules, but elution has sometimes been observed to be undesirably slow. In order to determine which physicochemical phenomena control elution behavior, commercially available cellulosic, dextran-grafted and unmodified agarose materials were characterized here by their elution profiles at various conditions, including different degrees of loading. Elution data were analyzed under the assumption of purely diffusion-limited control, including the role of pore structure properties such as porosity and tortuosity. In general, effective elution rates decreased with the reduction of accessible pore volume, but differences among different proteins indicated the roles of additional factors. Additional measurements and analysis, including the use of confocal laser scanning microscopy to observe elution within single chromatographic particles, indicated the importance of protein association within the particle during elution. The use of protein stabilizing agents was explored in systems presenting atypical elution behavior, and l-arginine and disaccharide excipients were shown to alleviate the effects for one protein, lysozyme, in the presence of sodium chloride. Incorporation of these excipients into eluent buffer gave rise to faster elution and significantly lower pool volumes in elution from polymer-modified adsorbents.

  2. Modeling the construction of polymeric adsorbent media: effects of counter-ions on ligand immobilization and pore structure.

    PubMed

    Riccardi, Enrico; Wang, Jee-Ching; Liapis, Athanasios I

    2014-02-28

    Molecular dynamics modeling and simulations are employed to study the effects of counter-ions on the dynamic spatial density distribution and total loading of immobilized ligands as well as on the pore structure of the resultant ion exchange chromatography adsorbent media. The results show that the porous adsorbent media formed by polymeric chain molecules involve transport mechanisms and steric resistances which cause the charged ligands and counter-ions not to follow stoichiometric distributions so that (i) a gradient in the local nonelectroneutrality occurs, (ii) non-uniform spatial density distributions of immobilized ligands and counter-ions are formed, and (iii) clouds of counter-ions outside the porous structure could be formed. The magnitude of these counter-ion effects depends on several characteristics associated with the size, structure, and valence of the counter-ions. Small spherical counter-ions with large valence encounter the least resistance to enter a porous structure and their effects result in the formation of small gradients in the local nonelectroneutrality, higher ligand loadings, and more uniform spatial density distributions of immobilized ligands, while the formation of exterior counter-ion clouds by these types of counter-ions is minimized. Counter-ions with lower valence charges, significantly larger sizes, and elongated shapes, encounter substantially greater steric resistances in entering a porous structure and lead to the formation of larger gradients in the local nonelectroneutrality, lower ligand loadings, and less uniform spatial density distributions of immobilized ligands, as well as substantial in size exterior counter-ion clouds. The effects of lower counter-ion valence on pore structure, local nonelectroneutrality, spatial ligand density distribution, and exterior counter-ion cloud formation are further enhanced by the increased size and structure of the counter-ion. Thus, the design, construction, and functionality of

  3. Removal of copper ions from aqueous solution by adlai shell (Coix lacryma-jobi L.) adsorbents.

    PubMed

    de Luna, Mark Daniel G; Flores, Edgar D; Cenia, Marie Chela B; Lu, Ming-Chun

    2015-09-01

    Adlai shell (Coix lacryma-jobi L.) adsorbents (ASA) were used to remove copper ions from aqueous solutions under batch conditions. The effect of physical and chemical modification of ASA on Cu(II) removal was evaluated. Results showed that the high coefficients of determination for the pseudo-second order (R(2) > 0.9999) and for the intraparticle diffusion (R(2) > 0.9843) equations indicate that the rate-determining step is a combination of pore diffusion and chemisorption at low Cu(II) concentration and boundary layer, pore diffusion and chemisorption at high Cu(II) concentration. At 298K and 100 mg L(-1) Cu(II), the computed qe and k2 values were 17.2 mg g(-1) and 0.012 g mg(-1) min(-1), respectively. The Freundlich model (R(2) > 0.9636) adequately describes the experimental data indicating heterogeneous adsorption. Overall, the results of the study demonstrate the potential of adlai shell adsorbents for the removal of heavy metals from aqueous solutions. PMID:26081160

  4. Alkaline deoxygenated graphene oxide as adsorbent for cadmium ions removal from aqueous solutions.

    PubMed

    Liu, Jun; Du, Hongyan; Yuan, Shaowei; He, Wanxia; Yan, Pengju; Liu, Zhanhong

    2015-01-01

    Alkaline deoxygenated graphene oxide (aGO) was prepared through alkaline hydrothermal treatment and used as adsorbent to remove Cd(II) ions from aqueous solutions for the first time. The characterization results of transmission electron microscopy, X-ray diffraction, Raman spectroscopy, and Fourier transform infrared (FT-IR) spectra indicate that aGO was successfully synthesized. The batch adsorption experiments showed that the adsorption kinetics could be described by the pseudo-second-order kinetic model, and the isotherms equilibrium data were well fitted with the Langmuir model. The maximum adsorption capacity of Cd(II) on aGO was 156 mg/g at pH 5 and T=293 K. The adsorption thermodynamic parameters indicated that the adsorption process was a spontaneous and endothermic reaction. The mainly adsorption mechanism speculated from FT-IR results may be attributed to the electrostatic attraction between Cd2+ and negatively charged groups (-CO-) of aGO and cation-π interaction between Cd2+ and the graphene planes. The findings of this study demonstrate the potential utility of the nanomaterial aGO as an effective adsorbent for Cd(II) removal from aqueous solutions. PMID:26038925

  5. Custom-tailored adsorbers: A molecular dynamics study on optimal design of ion exchange chromatography material.

    PubMed

    Lang, Katharina M H; Kittelmann, Jörg; Pilgram, Florian; Osberghaus, Anna; Hubbuch, Jürgen

    2015-09-25

    The performance of functionalized materials, e.g., ion exchange resins, depends on multiple resin characteristics, such as type of ligand, ligand density, the pore accessibility for a molecule, and backbone characteristics. Therefore, the screening and identification process for optimal resin characteristics for separation is very time and material consuming. Previous studies on the influence of resin characteristics have focused on an experimental approach and to a lesser extent on the mechanistic understanding of the adsorption mechanism. In this in silico study, a previously developed molecular dynamics (MD) tool is used, which simulates any given biomolecule on resins with varying ligand densities. We describe a set of simulations and experiments with four proteins and six resins varying in ligand density, and show that simulations and experiments correlate well in a wide range of ligand density. With this new approach simulations can be used as pre-experimental screening for optimal adsorber characteristics, reducing the actual number of screening experiments, which results in a faster and more knowledge-based development of custom-tailored adsorbers.

  6. Removal of copper ions from aqueous solution by adlai shell (Coix lacryma-jobi L.) adsorbents.

    PubMed

    de Luna, Mark Daniel G; Flores, Edgar D; Cenia, Marie Chela B; Lu, Ming-Chun

    2015-09-01

    Adlai shell (Coix lacryma-jobi L.) adsorbents (ASA) were used to remove copper ions from aqueous solutions under batch conditions. The effect of physical and chemical modification of ASA on Cu(II) removal was evaluated. Results showed that the high coefficients of determination for the pseudo-second order (R(2) > 0.9999) and for the intraparticle diffusion (R(2) > 0.9843) equations indicate that the rate-determining step is a combination of pore diffusion and chemisorption at low Cu(II) concentration and boundary layer, pore diffusion and chemisorption at high Cu(II) concentration. At 298K and 100 mg L(-1) Cu(II), the computed qe and k2 values were 17.2 mg g(-1) and 0.012 g mg(-1) min(-1), respectively. The Freundlich model (R(2) > 0.9636) adequately describes the experimental data indicating heterogeneous adsorption. Overall, the results of the study demonstrate the potential of adlai shell adsorbents for the removal of heavy metals from aqueous solutions.

  7. Fragmentation of molecular adsorbates by electron and ion bombardment: methoxy chemistry on Al(111)

    SciTech Connect

    Basu, P.; Chen, J.G.; Ng, L.; Colaianni, M.L.; Yates, J.T.

    1988-08-15

    High-resolution electron-energy-loss spectroscopy (HR)EELS has been used successfully to provide direct spectroscopic evidence regarding details of the molecular fragmentation of methoxy (CH3O) on Al(lll) caused by energetic electron and ion beams. Chemisorbed methoxy on Al(lll) is produced by heating of absorbed CH3OH. Irradiation of CH3O(a) by either energetic (approx 300 eV) electrons or Ar+ ions results in C-O and C-H bond scission with simultaneous formation of Al-O and Al-C bonds. During electron stimulated desorption the CH3O(a) species undergo sequential fragmentation first to CHx groups that are captured by the surface and in the final decay process to adsorbed carbon. C-O bonds in CH3O9a) are depleted preferentially compared to C-H bonds in CHx(a) species. The electron-induced sequential fragmentation of the patent CH3 group (from methoxy) to resultant CHx(a) occurs with an efficiency approx. 3 orders of magnitude greater than the subsequent process of CHx(a)=C(a). Cross sections for various bond scission processes in electron and ion bombardment have been estimated.

  8. TEMPO-oxidized cellulose hydrogel as a high-capacity and reusable heavy metal ion adsorbent.

    PubMed

    Isobe, Noriyuki; Chen, Xiaoxia; Kim, Ung-Jin; Kimura, Satoshi; Wada, Masahisa; Saito, Tsuguyuki; Isogai, Akira

    2013-09-15

    Nitroxy radical catalyzed oxidation with hypochlorite/bromide (TEMPO-mediated oxidation) was performed on a cellulose hydrogel prepared using LiOH/urea solvent. TEMPO oxidation successfully introduced carboxyl groups onto the surface of the cellulose hydrogel with retention of the gel structure and its nanoporous property. The equilibrium measurement of Cu(2+) adsorption showed favorable interaction with Cu(2+) and high maximum adsorption capacity. In addition, over 98% of the adsorbed Cu(2+) was recovered using acid treatment, and the subsequent washing allowed the TEMPO-oxidized gels to be used repeatedly. Furthermore, the TEMPO-oxidized cellulose hydrogel showed high adsorption capacity for other toxic metal ions such as Zn(2+), Fe(3+), Cd(2+), and Cs(+).

  9. Oxygen ion-conducting dense ceramic

    DOEpatents

    Balachandran, Uthamalingam; Kleefisch, Mark S.; Kobylinski, Thaddeus P.; Morissette, Sherry L.; Pei, Shiyou

    1998-01-01

    Preparation, structure, and properties of mixed metal oxide compositions and their uses are described. Mixed metal oxide compositions of the invention have stratified crystalline structure identifiable by means of powder X-ray diffraction patterns. In the form of dense ceramic membranes, the present compositions demonstrate an ability to separate oxygen selectively from a gaseous mixture containing oxygen and one or more other volatile components by means of ionic conductivities.

  10. Water and ion transport in ultra-adsorbing porous magnesium carbonate studied by dielectric spectroscopy

    NASA Astrophysics Data System (ADS)

    Pochard, Isabelle; Frykstrand, Sara; Ahlström, Olle; Forsgren, Johan; Strømme, Maria

    2014-01-01

    Porous materials are used in application areas ranging from drug and vaccine delivery, medical implants, molecular sieves and cosmetics to catalysis and humidity control. In the present work, we employed an alternative approach to gain in-depth understanding about water interaction properties in such materials by the use of dielectric spectroscopy and thereby show that it is possible to obtain information that is not accessible from the more commonly employed water interaction analysis techniques. Specifically, the complex dielectric response of Upsalite, a novel, super-hydroscopic, high-surface area, porous magnesium carbonate material was measured in isothermal frequency scans between 10-3 and 106 Hz at controlled relative humidity (RH). We found the dielectric constant of the dry material to be 1.82. The ratio of bound to free water present in Upsalite after adsorption at room temperature was found to be high irrespective of the surrounding humidity with values ranging from ˜67% to ˜90%. We further found that OH- ions are the charge carriers responsible for the electrode polarization observed in the dielectric response and that the amount of these ions that are free to move in the material corresponds to a concentration of the order of 1-10 μmol l-1 independent of RH. Finally, the OH- diffusion coefficient displayed a drastic decrease with decreasing RH, typical of transport in unsaturated conditions. The presented results provide detailed insight about water interactions in the novel water adsorbing material under study and it is foreseen that the employed analysis methods can be used to evaluate other types of moisture adsorbing materials as well as the movement of functional species in the pores of inorganic drug delivery materials and materials tailored for adsorption of harmful charged species.

  11. Facile preparation of highly hydrophilic, recyclable high-performance polyimide adsorbents for the removal of heavy metal ions.

    PubMed

    Huang, Jieyang; Zheng, Yaxin; Luo, Longbo; Feng, Yan; Zhang, Chaoliang; Wang, Xu; Liu, Xiangyang

    2016-04-01

    To obtain high-performance adsorbents that combine excellent adsorption ability, thermal stability, service life and recycling ability, polyimide (PI)/silica powders were prepared via a facile one-pot coprecipitation process. A benzimidazole unit was introduced into the PI backbone as the adsorption site. The benzimidazole unit induced more hydroxyls onto the silica, which provided hydrophilic sites for access by heavy metal ions. By comprehensively analyzing the effect of hydrophilcity, agglomeration, silica polycondensation, specific surface area and PI crystallinity, 10% was demonstrated to be the most proper feed silica content. The equilibrium adsorption amount (Qe) for Cu(2+) of PI/silica adsorbents was 77 times higher than that of pure PI. Hydrogen chloride (HCl) was used as a desorbent for heavy metal ions and could be decomplexed with benzimidazole unit at around 300°C, which was lower than the glass transition temperature of PI. The complexation and decomplexation process of HCl made PI/silica adsorbents recyclable, and the adsorption ability remained steady for more than 50 recycling processes. As PI/silica adsorbents possess excellent thermal stability, chemical resistance and radiation resistance and hydrophilicity, they have potential as superior recyclable adsorbents for collecting heavy metal ions from waste water in extreme environments. PMID:26736172

  12. Novel fungus-titanate bio-nanocomposites as high performance adsorbents for the efficient removal of radioactive ions from wastewater.

    PubMed

    Xu, Mingze; Wei, Guodong; Liu, Na; Zhou, Liang; Fu, Chengwei; Chubik, M; Gromov, A; Han, Wei

    2014-01-21

    Reclaimable adsorbents have a critical application in the adsorption of radioactive materials. In this study, the novel bio-nanocomposites comprising fungi and titanate nanotubes are successfully synthesized by a simple and low-cost method. Morphological characterizations and composite mechanism analysis confirm that the composites are sufficiently stable to avoid dust pollution resulting from the titanate nanomaterials. Adsorption experiments demonstrate that the bio-nanocomposites are efficient adsorbents with a saturated sorption capacity as high as 120 mg g(-1) (1.75 meq. g(-1)) for Ba(2+) ions. The results suggest that the bio-nanocomposites can be used as promising radioactive adsorbents for removing radioactive ions from water caused by nuclear leakage.

  13. Inhomogeneous depletion of oxygen ions in metal oxide nanoparticles

    NASA Astrophysics Data System (ADS)

    Vykhodets, Vladimir B.; Jarvis, Emily A. A.; Kurennykh, Tatiana E.; Beketov, Igor V.; Obukhov, Sviatoslav I.; Samatov, Oleg M.; Medvedev, Anatoly I.; Davletshin, Andrey E.; Whyte, Travis H.

    2016-02-01

    Zirconia and yttria stabilized zirconia (YSZ) have multiple uses, including catalysis, fuel cells, dental applications, and thermal coatings. We employ nuclear reaction analysis to determine elemental composition of YSZ nanoparticles synthesized by laser evaporation including 18O studies to distinguish between oxide and adsorbed oxygen content as a function of surface area. We see dramatic deviation from stoichiometry that can be traced to loss of oxygen from the oxide near the surface of these nanopowders. Density functional calculations are coupled with these experimental studies to explore the electronic structure of nonstoichiometric surfaces achieved through depletion of oxygen. Our results show oxygen-depleted surfaces present under oxygen potentials where stoichiometric, oxygen-terminated surfaces would be favored thermodynamically for crystalline systems. Oxygen depletion at nanopowder surfaces can create effective two-dimensional surface metallic states while maintaining stoichiometry in the underlying nanoparticle core. This insight into nanopowder surfaces applies to dissimilar oxides of aluminum and zirconium indicating synthesis conditions may be more influential than the inherent oxide properties and displaying need for distinct models for nanopowders of these important engineering materials where surface chemistry dominates performance.

  14. Novel fungus-titanate bio-nanocomposites as high performance adsorbents for the efficient removal of radioactive ions from wastewater

    NASA Astrophysics Data System (ADS)

    Xu, Mingze; Wei, Guodong; Liu, Na; Zhou, Liang; Fu, Chengwei; Chubik, M.; Gromov, A.; Han, Wei

    2013-12-01

    Reclaimable adsorbents have a critical application in the adsorption of radioactive materials. In this study, the novel bio-nanocomposites comprising fungi and titanate nanotubes are successfully synthesized by a simple and low-cost method. Morphological characterizations and composite mechanism analysis confirm that the composites are sufficiently stable to avoid dust pollution resulting from the titanate nanomaterials. Adsorption experiments demonstrate that the bio-nanocomposites are efficient adsorbents with a saturated sorption capacity as high as 120 mg g-1 (1.75 meq. g-1) for Ba2+ ions. The results suggest that the bio-nanocomposites can be used as promising radioactive adsorbents for removing radioactive ions from water caused by nuclear leakage.Reclaimable adsorbents have a critical application in the adsorption of radioactive materials. In this study, the novel bio-nanocomposites comprising fungi and titanate nanotubes are successfully synthesized by a simple and low-cost method. Morphological characterizations and composite mechanism analysis confirm that the composites are sufficiently stable to avoid dust pollution resulting from the titanate nanomaterials. Adsorption experiments demonstrate that the bio-nanocomposites are efficient adsorbents with a saturated sorption capacity as high as 120 mg g-1 (1.75 meq. g-1) for Ba2+ ions. The results suggest that the bio-nanocomposites can be used as promising radioactive adsorbents for removing radioactive ions from water caused by nuclear leakage. Electronic supplementary information (ESI) available: The experimental section and supplementary figures are shown in supplementary information. See DOI: 10.1039/c3nr03467d

  15. Characterization of cross-linked cellulosic ion-exchange adsorbents: 2. Protein sorption and transport.

    PubMed

    Angelo, James M; Cvetkovic, Aleksandar; Gantier, Rene; Lenhoff, Abraham M

    2016-03-18

    Adsorption behavior in the HyperCel family of cellulosic ion-exchange materials (Pall Corporation) was characterized using methods to assess, quantitatively and qualitatively, the dynamics of protein uptake as well as static adsorption as a function of ionic strength and protein concentration using several model proteins. The three exchangers studied all presented relatively high adsorptive capacities under low ionic strength conditions, comparable to commercially available resins containing polymer functionalization aimed at increasing that particular characteristic. The strong cation- and anion-exchange moieties showed higher sensitivity to increasing salt concentrations, but protein affinity on the salt-tolerant STAR AX HyperCel exchanger remained strong at ionic strengths normally used in downstream processing to elute material fully during ion-exchange chromatography. Very high uptake rates were observed in both batch kinetics experiments and time-series confocal laser scanning microscopy, suggesting low intraparticle transport resistances relative to external film resistance, even at higher bulk protein concentrations where the opposite is typically observed. Electron microscopy imaging of protein adsorbed phases provided additional insight into particle structure that could not be resolved in previous work on the bare resins.

  16. A new ion-exchange adsorbent with paramagnetic properties for the separation of genomic DNA.

    PubMed

    Feng, Guodong; Jiang, Luan; Wen, Puhong; Cui, Yali; Li, Hong; Hu, Daodao

    2011-11-21

    A new ion-exchange adsorbent (IEA) derived from Fe(3)O(4)/SiO(2)-GPTMS-DEAE with paramagnetic properties was prepared. Fe(3)O(4) nanoparticles were firstly prepared in water-in-oil microemulsion. The magnetic Fe(3)O(4) particles were modified in situ by hydrolysis and condensation reactions with tetraethoxysilane (TEOS) to form the core-shell Fe(3)O(4)/SiO(2). The modified particles were further treated by 3-glycidoxypropyltrimethoxysilane (GPTMS) to form Fe(3)O(4)/SiO(2)-GPTMS nanoparticles. Fe(3)O(4)/SiO(2)-GPTMS-DEAE nanoparticles (IEA) were finally obtained through the condensation reaction between the Cl of diethylaminoethyl chloride-HCl (DEAE) and the epoxy groups of GPTMS in the Fe(3)O(4)/SiO(2)-GPTMS. The obtained IEA has features of paramagnetic and ion exchange properties because of the Fe(3)O(4) nanoparticles and protonated organic amine in the sample. The intermediates and final product obtained in the synthesis process were characterized. The separation result of genomic DNA from blood indicated that Fe(3)O(4)/SiO(2)-GPTMS-DEAE nanoparticles have outstanding advantages in operation, selectivity, and capacity. PMID:21966668

  17. Effects of surface adsorbed oxygen, applied voltage, and temperature on UV photoresponse of ZnO nanorods

    NASA Astrophysics Data System (ADS)

    Zong, Xian-Li; Zhu, Rong

    2015-10-01

    The ultraviolet (UV) photoresponses of ZnO nanorods directly grown on and between two micro Au-electrodes by using electric-field-assisted wet chemical method are measured comprehensively under different conditions, including ambient environment, applied bias voltage, gate voltage and temperature. Experimental results indicate that the photoresponses of the ZnO nanorods can be modulated by surface oxygen adsorptions, applied voltages, as well as temperatures. A model taking into account both surface adsorbed oxygen and electron-hole activities inside ZnO nanorods is proposed. The enhancement effect of the bias voltage on photoresponse is also analyzed. Experimental results shows that the UV response time (to 63%) of ZnO nanorods in air and at 59 °C could be shortened from 34.8 s to 0.24 s with a bias of 4 V applied between anode and cathode. Project supported by the National Natural Science Foundation of China (Grant No. 91123017).

  18. A theoretical study of the interaction of hydrogen and oxygen with palladium or gold adsorbed on pyridine-like nitrogen-doped graphene.

    PubMed

    Rangel, Eduardo; Magana, Luis Fernando; Sansores, Luis Enrique

    2014-12-15

    The interaction of H2 and O2 molecules in the presence of nitrogen-doped graphene decorated with either a palladium or gold atom was investigated by using density functional theory. It was found that two hydrogen molecules were adsorbed on the palladium atom. The interaction of these adsorbed hydrogen molecules with two oxygen molecules generates two hydrogen peroxide molecules first through a Eley-Rideal mechanism and then through a Langmuir-Hinshelwood mechanism. The barrier energies for this reaction were small; therefore, we expect that this process may occur spontaneously at room temperature. In the case of gold, a single hydrogen molecule is adsorbed and dissociated on the metal atom. The interaction of the dissociated hydrogen molecule on the surface with one oxygen molecule generates a water molecule. The competitive adsorption between oxygen and hydrogen molecules slightly favors oxygen adsorption.

  19. Simultaneous observations of electrostatic oxygen cyclotron waves and ion conics

    NASA Technical Reports Server (NTRS)

    Kintner, P. M.; Scales, W.; Vago, J.; Arnoldy, R.; Garbe, G.; Moore, T.

    1989-01-01

    A sounding rocket launched to 927 km apogee during an auroral substorm encountered regions of large quasi-static electric fields (not greater than 400 mV/m), ion conics (up to 700 eV maximum observed energy), and fluctuating electric fields near the oxygen cyclotron frequency. Since the fluctuating electric fields frequently exhibited spectral peaks just above the local oxygen cyclotron frequency, and since the fluctuating electric fields were linearly polarized, they are positively identified as electrostatic oxygen cyclotron waves (EOCW). The maximum amplitude of the EOCW was about 5 mV/m rms. The EOCW closely correlated with the presence of ion conics. Because of the relatively low amplitude of the EOCW and their relatively low coherence, it cannot be concluded that they are solely responsible for the production of the ion conics.

  20. Interphase Evolution of a Lithium-Ion/Oxygen Battery.

    PubMed

    Elia, Giuseppe Antonio; Bresser, Dominic; Reiter, Jakub; Oberhumer, Philipp; Sun, Yang-Kook; Scrosati, Bruno; Passerini, Stefano; Hassoun, Jusef

    2015-10-14

    A novel lithium-ion/oxygen battery employing Pyr14TFSI-LiTFSI as the electrolyte and nanostructured LixSn-C as the anode is reported. The remarkable energy content of the oxygen cathode, the replacement of the lithium metal anode by a nanostructured stable lithium-alloying composite, and the concomitant use of nonflammable ionic liquid-based electrolyte result in a new and intrinsically safer energy storage system. The lithium-ion/oxygen battery delivers a stable capacity of 500 mAh g(-1) at a working voltage of 2.4 V with a low charge-discharge polarization. However, further characterization of this new system by electrochemical impedance spectroscopy, scanning electron microscopy, and energy-dispersive X-ray spectroscopy reveals the progressive decrease of the battery working voltage, because of the crossover of oxygen through the electrolyte and its direct reaction with the LixSn-C anode.

  1. Interphase Evolution of a Lithium-Ion/Oxygen Battery.

    PubMed

    Elia, Giuseppe Antonio; Bresser, Dominic; Reiter, Jakub; Oberhumer, Philipp; Sun, Yang-Kook; Scrosati, Bruno; Passerini, Stefano; Hassoun, Jusef

    2015-10-14

    A novel lithium-ion/oxygen battery employing Pyr14TFSI-LiTFSI as the electrolyte and nanostructured LixSn-C as the anode is reported. The remarkable energy content of the oxygen cathode, the replacement of the lithium metal anode by a nanostructured stable lithium-alloying composite, and the concomitant use of nonflammable ionic liquid-based electrolyte result in a new and intrinsically safer energy storage system. The lithium-ion/oxygen battery delivers a stable capacity of 500 mAh g(-1) at a working voltage of 2.4 V with a low charge-discharge polarization. However, further characterization of this new system by electrochemical impedance spectroscopy, scanning electron microscopy, and energy-dispersive X-ray spectroscopy reveals the progressive decrease of the battery working voltage, because of the crossover of oxygen through the electrolyte and its direct reaction with the LixSn-C anode. PMID:26389522

  2. Activation of oxygen-mediating pathway using copper ions: fine-tuning of growth kinetics in gold nanorod overgrowth.

    PubMed

    Liu, Wenqi; Zhang, Hui; Wen, Tao; Yan, Jiao; Hou, Shuai; Shi, Xiaowei; Hu, Zhijian; Ji, Yinglu; Wu, Xiaochun

    2014-10-21

    Growth kinetics plays an important role in the shape control of nanocrystals (NCs). Herein, we presented a unique way to fine-tune the growth kinetics via oxidative etching activated by copper ions. For the overgrowth of gold nanorods (Au NRs), competitive adsorption of dissolved oxygen on rod surface was found to slow down the overgrowth rate. Copper ions were able to remove the adsorbed oxygen species from the Au surface via oxidative etching, thus exposing more reaction sites for Au deposition. In this way, copper ions facilitated the overgrowth process. Furthermore, Cu(2+) rather than Cu(+) acted as the catalyst for the oxidative etching. Comparative study with Ag(+) indicated that Cu(2+) cannot regulate NC shapes via an underpotential deposition mechanism. In contrast, Ag(+) led to the formation of Au tetrahexahedra (THH) and a slight decrease of the growth rate at similar growth conditions. Combining the distinct roles of the two ions enabled elongated THH to be produced. Copper ions activating the O2 pathway suggested that dissolved oxygen has a strong affinity for the Au surface. Moreover, the results of NC-sensitized singlet oxygen ((1)O2) indicated that the absorbed oxygen species on the surface of Au NCs bounded with low-index facets mainly existed in the form of molecular O2. PMID:25244407

  3. K-shell Photoabsorption of Oxygen Ions

    NASA Technical Reports Server (NTRS)

    Garcia, J.; Mendoza, C.; Bautista, M. A.; Gorczyca, T. W.; Kallman, T. R.; Palmeri, P.

    2005-01-01

    The high spectral resolutions of the Chandra and XMM-Newton X-ray observatories have unveiled the useful diagnostic possibilities of oxygen K absorption. To mention a few, strong O VII and O VIII edges are almost ubiquitous in the spectra of Seyfert 1 galaxies which have been used by Lee et al. (2001) to predict of a warm dust absorber along the line of sight; although this conclusion has been criticized in the light of a data reanalysis (SA0 et al. 2003), Steenbrugge et al. (2003) have detected inner-shell transitions of O III-O VI in the spectrum of NGC 5548 that point to a warm absorber that spans three orders of magnitude in ionization parameter. Moreover, Behar et al. (2003) have stressed that, in the case of both Seyfert 1 and Seyfert 2 galaxies, a broad range of oxygen charge states are usually observed along the line of sight that must be fitted simultaneously, and may imply strong density gradients of 2-4 orders of magnitude over short distances.

  4. A [sup 13]C NMR study of ethylene adsorbed on reduced and oxygen-covered Ag surfaces

    SciTech Connect

    Plischke, J.K.; Benesi, A.J.; Vannice, M.A. )

    1992-11-01

    [sup 13]C-enriched ethylene was adsorbed on both clean and oxygen-covered Ag particles dispersed on [eta]-Al[sub 2]O[sub 3]. Irreversibly adsorbed C[sub 2]H[sub 4] on O-covered Ag exhibited an upfield shift of [minus]20 ppm relative to gas-phase C[sub 2]H[sub 4], whereas a narrower line and smaller shift of [minus]5 ppm occurred for C[sub 2]H[sub 4] reversibly adsorbed on reduced Ag. In addition to the resonance at 103 ppm for irreversibly adsorbed C[sub 2]H[sub 4], CP/MAS NMR spectra also gave resonances at 179, 170, 164, 159, and 19 ppm for the O-covered Ag sample. The CP/MAS spectrum for Ag acetate powder clearly identified the 179- and 19-ppm peaks as those associated with the carboxyl and methyl carbons of the acetate anion, and the peaks at 159, 164, and 170 ppm were assigned to oxalate, formate, and carbonate (or possibly acetic anhydride) species, respectively, based on previous studies. When heated to 473 K the adsorbed C[sub 2]H[sub 4] disappeared and only acetate and oxalate groups were observed, and continued heating to 573 K removed almost all resonances. No C[sub 2]H[sub 4]O was unambiguously detected, thus with this unpromoted Ag catalyst utilizing a high-surface-area alumina the observable surface species appeared to be those associated with complete combustion, with acetate and oxalate predominating during reaction. These results directly confirm the presence of an Ag acetate species which has been proposed previously to be an intermediate in complete combustion, and the presence of the other three species support earlier tentative assignments based on IR and TPR spectroscopy. Chemical shifts at 61, 28, and 13 ppm were indicative of alkoxy species formed on Bronsted-acid sites on the Al[sub 2]O[sub 3] surface. 58 refs., 8 figs., 4 tabs.

  5. Activated boron nitride as an effective adsorbent for metal ions and organic pollutants.

    PubMed

    Li, Jie; Xiao, Xing; Xu, Xuewen; Lin, Jing; Huang, Yang; Xue, Yanming; Jin, Peng; Zou, Jin; Tang, Chengchun

    2013-01-01

    Novel activated boron nitride (BN) as an effective adsorbent for pollutants in water and air has been reported in the present work. The activated BN was synthesized by a simple structure-directed method that enabled us to control the surface area, pore volume, crystal defects and surface groups. The obtained BN exhibits an super high surface area of 2078 m(2)/g, a large pore volume of 1.66 cm(3)/g and a special multimodal microporous/mesoporous structure located at ~ 1.3, ~ 2.7, and ~ 3.9 nm, respectively. More importantly, the novel activated BN exhibits an excellent adsorption performance for various metal ions (Cr(3+), Co(2+), Ni(2+), Ce(3+), Pb(2+)) and organic pollutants (tetracycline, methyl orange and congo red) in water, as well as volatile organic compounds (benzene) in air. The excellent reusability of the activated BN has also been confirmed. All the features render the activated BN a promising material suitable for environmental remediation. PMID:24220570

  6. Activated boron nitride as an effective adsorbent for metal ions and organic pollutants

    PubMed Central

    Li, Jie; Xiao, Xing; Xu, Xuewen; Lin, Jing; Huang, Yang; Xue, Yanming; Jin, Peng; Zou, Jin; Tang, Chengchun

    2013-01-01

    Novel activated boron nitride (BN) as an effective adsorbent for pollutants in water and air has been reported in the present work. The activated BN was synthesized by a simple structure-directed method that enabled us to control the surface area, pore volume, crystal defects and surface groups. The obtained BN exhibits an super high surface area of 2078 m2/g, a large pore volume of 1.66 cm3/g and a special multimodal microporous/mesoporous structure located at ~ 1.3, ~ 2.7, and ~ 3.9 nm, respectively. More importantly, the novel activated BN exhibits an excellent adsorption performance for various metal ions (Cr3+, Co2+, Ni2+, Ce3+, Pb2+) and organic pollutants (tetracycline, methyl orange and congo red) in water, as well as volatile organic compounds (benzene) in air. The excellent reusability of the activated BN has also been confirmed. All the features render the activated BN a promising material suitable for environmental remediation. PMID:24220570

  7. Detection of molecular oxygen adsorbate during room-temperature oxidation of Si(100)2 × 1 surface: In situ synchrotron radiation photoemission study

    NASA Astrophysics Data System (ADS)

    Yoshigoe, Akitaka; Yamada, Yoichi; Taga, Ryo; Ogawa, Shuichi; Takakuwa, Yuji

    2016-10-01

    Synchrotron radiation photoelectron spectroscopy during the oxidation of a Si(100)2 × 1 surface at room temperature revealed the existence of molecularly adsorbed oxygen, which was considered to be absent. The O 1s spectrum of such oxidation was found to be similar to that of Si(111)7 × 7 surface oxidation. Also, molecular oxygen appeared after the initial surface oxides were formed, indicating that it was not a precursor for dissociation oxygen adsorption on a clean surface. Considering this finding, we have proposed presumable structural models for atomic configurations, where molecular oxygen resided on the oxidized silicon with two oxygen atoms at the backbonds.

  8. Electron structure of AgCl nanocrystal with silver ion adsorbed on atomic-rough surface and quantum transitions

    NASA Astrophysics Data System (ADS)

    Timoshenko, Yury K.; Shunina, Valentina A.

    2009-08-01

    Adsorption was considered as on the atomically-rough surface (near the step and step fracture) as on the smooth surface. The electron structure of AgCl nanocrystals with the adsorbed silver ion were calculated by semiempirical tight-binding method relying on a self-consistent approach for the effective charges and dipole moments of the ions and in frame of DFT method B3LYP/HW. The quantum transitions were investigated in semiempirical approach. Visualization of the wave functions was performed for the localized states. Basing on the obtained data a conclusion is specically made that one can expect an enhancement of photoelectron localization with a decrease of the anions number in the substrate nearest to the adsorbed ion. It means that the most ecient trapping of photoelectron should occur under adsorption on a smooth surface rather than near the steps and their fractures as it was assumed previously. Also probabilities of quantum transitions for AgCl : J nanocrystal with the adsorbed silver ion were been discussed. This work is a continuation of paper [1].

  9. Removal of chemical oxygen demand from landfill leachate using cow-dung ash as a low-cost adsorbent.

    PubMed

    Kaur, Kamalpreet; Mor, Suman; Ravindra, Khaiwal

    2016-05-01

    The application of cow dung ash was assessed for the removal of organic contamination from the wastewater using landfill leachate of known Chemical Oxygen Demand (COD) concentration in batch mode. The effect of various parameters like adsorbents dose, time, pH and temperature was investigated. Results indicate that upto 79% removal of COD could be achieved using activated cow dung ash (ACA) at optimum temperature of 30 °C at pH 6.0 using 20 g/L dose in 120 min, whereas cow dung ash (CA) shows 66% removal at pH 8.0 using 20 g/L dose, also in 120 min. Data also shows that ACA exhibited 11-13% better removal efficiency than CA. COD removal efficiency of various adsorbents was also compared and it was found that ACA offers significantly higher efficiency. Freundlich and Langmuir adsorption isotherms were also applied, which depicts good correlations (0.921 and 0.976) with the experimental data. Scanning electron microscope (SEM) images shows that after the activation, carbon particles disintegrate and surface of particles become more rough and porous, indicating the reason for high adsorption efficiency of ACA. Hence, ACA offers a cost-effective solution for the removal of organic contaminants from the wastewater and for the direct treatment of landfill leachate.

  10. Aging effect in magnetotransport property of oxygen adsorbed BaFe{sub 2}As{sub 2}

    SciTech Connect

    Ghosh, Nilotpal E-mail: nilotpal@vit.ac.in; Raj, Santhosh

    2015-06-24

    Presence of oxygen (O{sub 2}) has been found by Energy Dispersive X-ray Analysis (EDAX) on the surfaces of flux grown BaFe{sub 2}As{sub 2} single crystals which were kept in air ambience for several months. Transport studies show that the O{sub 2} adsorbed crystals are more resistive and do not display any sharp slope change near 140 K which is the well known Spin Density Wave (SDW) transition temperature (T{sub SDW}) accompanying structural transition for as grown BaFe{sub 2}As{sub 2}. An anomalous slope change in resistivity is observed around 18 K at 0 and 5T. Magnetoresistance (MR) is noticed to increase as a function of applied field (H) quite differently than that for as grown crystals below T{sub SDW} which may be attributed to aging effect.

  11. The Role of Oxygen in the Formation of TNT Product Ions in Ion Mobility Spectrometry

    SciTech Connect

    Daum, Keith Alvin; Atkinson, David Alan; Ewing, Robert Gordon

    2002-03-01

    The atmospheric pressure ionization of 2,4,6-trinitrotoluene (TNT) in air yields the (TNT-H)- product ion. It is generally accepted that this product ion is formed by the direct proton abstraction of neutral TNT by O2- reactant ions. Data presented here demonstrate the reaction involves the formation of an intermediate (TNT·O2)-, from the association of either TNT+O2- or TNT-+O2. This intermediate has two subsequent reaction branches. One of these branches involves simple dissociation of the intermediate to TNT-; the other branch is a terminal reaction that forms the typically observed (TNT-H)- ion via proton abstraction. The dissociation reaction involving electron transfer to TNT- appeared to be kinetically favored and prevailed at low concentrations of oxygen (less than 2%). The presence of significant amounts of oxygen, however, resulted in the predominant formation of the (TNT-H)- ion by the terminal reaction branch. With TNT- in the system, either from direct electron attachment or by simple dissociation of the intermediate, increasing levels of oxygen in the system will continue to reform the intermediate, allowing the cycle to continue until proton abstraction occurs. Key to understanding this complex reaction pathway is that O2- was observed to transfer an electron directly to neutral TNT to form the TNT-. At oxygen levels of less than 2%, the TNT- ion intensity increased with increasing levels of oxygen (and O2-) and was larger than the (TNT-H)- ion intensity. As the oxygen level increased from 2 to 10%, the (TNT-H)- product ion became predominant. The potential reaction mechanisms were investigated with an ion mobility spectrometer, which was configured to independently evaluate the ionization pathways.

  12. Modified Cr valence in symmetric oxygen ion conducting half cells with ion flow

    NASA Astrophysics Data System (ADS)

    Finsterbusch, Martin; Lussier, Alexandre; Negusse, Ezana; Idzerda, Yves

    2010-03-01

    The degradation mechanisms in ion conducting materials, including solid oxide fuel cells (SOFC), are still of high interest in current energy research, especially with regards to material and interface stability, fuel impurities and impurities originating from sealing or interconnect materials. A common practice is the use of symmetric half-cells (e.g. cathode/electrolyte/cathode) to determine interface stability via cross section Energy Dispersive x-ray Spectroscopy line scans and overpotential magnitude and degradation via AC-impedance spectroscopy. Using these electrically driven half-cells, we have developed a new method to directly measure degradation due to oxygen ion flow through ion conducting materials and their associated interface structures. By using X-ray absorption spectroscopy of cells before and after oxygen ion flow (800 C for 100 hours), we determined that the valence state of Cr that migrated from a metallic interconnect into the porous cathode changes in valence from +3 (Cr2O3) to +6 (CrO3), depending on the direction of the oxygen ion flow. This observation is strong evidence of the influence of the oxygen ion flux on the degradation mechanisms of ion conducting materials.

  13. Effect of Oxygen Adsorbates on Terahertz Emission Properties of Various Semiconductor Surfaces Covered with Graphene

    NASA Astrophysics Data System (ADS)

    Bagsican, Filchito Renee; Zhang, Xiang; Ma, Lulu; Wang, Minjie; Murakami, Hironaru; Vajtai, Robert; Ajayan, Pulickel M.; Kono, Junichiro; Tonouchi, Masayoshi; Kawayama, Iwao

    2016-11-01

    We have studied coherent terahertz (THz) emission from graphene-coated surfaces of three different semiconductors—InP, GaAs, and InAs—to provide insight into the influence of O2 adsorption on charge states and dynamics at the graphene/semiconductor interface. The amplitude of emitted THz radiation from graphene-coated InP was found to change significantly upon desorption of O2 molecules by thermal annealing, while THz emission from bare InP was nearly uninfluenced by O2 desorption. In contrast, the amount of change in the amplitude of emitted THz radiation due to O2 desorption was essentially the same for graphene-coated GaAs and bare GaAs. However, in InAs, neither graphene coating nor O2 adsorption/desorption affected the properties of its THz emission. These results can be explained in terms of the effects of adsorbed O2 molecules on the different THz generation mechanisms in these semiconductors. Furthermore, these observations suggest that THz emission from graphene-coated semiconductors can be used for probing surface chemical reactions (e.g., oxidation) as well as for developing O2 gas sensor devices.

  14. Effect of Oxygen Adsorbates on Terahertz Emission Properties of Various Semiconductor Surfaces Covered with Graphene

    NASA Astrophysics Data System (ADS)

    Bagsican, Filchito Renee; Zhang, Xiang; Ma, Lulu; Wang, Minjie; Murakami, Hironaru; Vajtai, Robert; Ajayan, Pulickel M.; Kono, Junichiro; Tonouchi, Masayoshi; Kawayama, Iwao

    2016-07-01

    We have studied coherent terahertz (THz) emission from graphene-coated surfaces of three different semiconductors—InP, GaAs, and InAs—to provide insight into the influence of O2 adsorption on charge states and dynamics at the graphene/semiconductor interface. The amplitude of emitted THz radiation from graphene-coated InP was found to change significantly upon desorption of O2 molecules by thermal annealing, while THz emission from bare InP was nearly uninfluenced by O2 desorption. In contrast, the amount of change in the amplitude of emitted THz radiation due to O2 desorption was essentially the same for graphene-coated GaAs and bare GaAs. However, in InAs, neither graphene coating nor O2 adsorption/desorption affected the properties of its THz emission. These results can be explained in terms of the effects of adsorbed O2 molecules on the different THz generation mechanisms in these semiconductors. Furthermore, these observations suggest that THz emission from graphene-coated semiconductors can be used for probing surface chemical reactions (e.g., oxidation) as well as for developing O2 gas sensor devices.

  15. Self-assembled poly(N-methylaniline)-lignosulfonate spheres: from silver-ion adsorbent to antimicrobial material.

    PubMed

    Lü, Qiu-Feng; Zhang, Jia-Yin; Yang, Jun; He, Zhi-Wei; Fang, Chang-Qing; Lin, Qilang

    2013-08-12

    Self-assembled poly(N-methylaniline)-lignosulfonate (PNMA-LS) composite spheres with reactive silver-ion adsorbability were prepared from N-methylaniline by using lignosulfonate (LS) as a dispersant. The results show that the PNMA-LS composite consisted of spheres with good size distribution and an average diameter of 1.03-1.27 μm, and the spheres were assembled by their final nanofibers with an average diameter of 19-34 nm. The PNMA-LS composite spheres exhibit excellent silver-ion adsorption; the maximum adsorption capacity of silver ions is up to 2.16 g g(-1) at an adsorption temperature of 308 K. TEM and wide-angle X-ray results of the PNMA-LS composite spheres after absorption of silver ions show that silver ions are reduced to silver nanoparticles with a mean diameter of about 11.2 nm through a redox reaction between the PNMA-LS composite and the silver ions. The main adsorption mechanism between the PNMA-LS composite and the silver ions is chelation and redox adsorption. In particular, a ternary PNMA-LS-Ag composite achieved by using the reducing reaction between PNMA-LS composite spheres and silver ions can be used as an antibacterial material with high bactericidal rate of 99.95 and 99.99% for Escherichia coli and Staphylococcus aureus cells, respectively.

  16. Orientation-Controlled Electrocatalytic Efficiency of an Adsorbed Oxygen-Tolerant Hydrogenase.

    PubMed

    Heidary, Nina; Utesch, Tillmann; Zerball, Maximilian; Horch, Marius; Millo, Diego; Fritsch, Johannes; Lenz, Oliver; von Klitzing, Regine; Hildebrandt, Peter; Fischer, Anna; Mroginski, Maria Andrea; Zebger, Ingo

    2015-01-01

    Protein immobilization on electrodes is a key concept in exploiting enzymatic processes for bioelectronic devices. For optimum performance, an in-depth understanding of the enzyme-surface interactions is required. Here, we introduce an integral approach of experimental and theoretical methods that provides detailed insights into the adsorption of an oxygen-tolerant [NiFe] hydrogenase on a biocompatible gold electrode. Using atomic force microscopy, ellipsometry, surface-enhanced IR spectroscopy, and protein film voltammetry, we explore enzyme coverage, integrity, and activity, thereby probing both structure and catalytic H2 conversion of the enzyme. Electrocatalytic efficiencies can be correlated with the mode of protein adsorption on the electrode as estimated theoretically by molecular dynamics simulations. Our results reveal that pre-activation at low potentials results in increased current densities, which can be rationalized in terms of a potential-induced re-orientation of the immobilized enzyme. PMID:26580976

  17. Orientation-Controlled Electrocatalytic Efficiency of an Adsorbed Oxygen-Tolerant Hydrogenase

    PubMed Central

    Zerball, Maximilian; Horch, Marius; Millo, Diego; Fritsch, Johannes; Lenz, Oliver; von Klitzing, Regine; Hildebrandt, Peter; Fischer, Anna; Mroginski, Maria Andrea; Zebger, Ingo

    2015-01-01

    Protein immobilization on electrodes is a key concept in exploiting enzymatic processes for bioelectronic devices. For optimum performance, an in-depth understanding of the enzyme-surface interactions is required. Here, we introduce an integral approach of experimental and theoretical methods that provides detailed insights into the adsorption of an oxygen-tolerant [NiFe] hydrogenase on a biocompatible gold electrode. Using atomic force microscopy, ellipsometry, surface-enhanced IR spectroscopy, and protein film voltammetry, we explore enzyme coverage, integrity, and activity, thereby probing both structure and catalytic H2 conversion of the enzyme. Electrocatalytic efficiencies can be correlated with the mode of protein adsorption on the electrode as estimated theoretically by molecular dynamics simulations. Our results reveal that pre-activation at low potentials results in increased current densities, which can be rationalized in terms of a potential-induced re-orientation of the immobilized enzyme. PMID:26580976

  18. Effects of Surface Oxygen on the Performance of Carbon as an Anode in Lithium-Ion Batteries

    NASA Technical Reports Server (NTRS)

    Hung, Ching-Cheh; Clark, Gregory W.

    2001-01-01

    Carbon materials with similar bulk structure but different surface oxygen were compared for their performance as anodes in lithium-ion battery. The bulk structure was such that the graphene planes were perpendicular to the surface. Three types of surfaces were examined: surface containing C=O type oxygen. surface containing -O-C type oxygen, and surface containing high concentration of active sites. The test involved cycles of lithium insertion into and release from the carbon materials, which was in the half cells of carbon/saturated LiI-50/50 (vol %) EC and DMC/lithium. During the first cycle of lithium insertion, the presence of adsorbed oxygen, -O-C type oxygen, active carbon sites, and C=O type oxygen resulted in the formation of solid-electrolyte interface (SEI) when the carbon's voltage relative to lithium metal was >1.35, 1 to 1.35, 0.5 to 1, and 0.67 to 0.7 V, respectively. An optimum -O-C type oxygen and a minimum C=O type oxygen was found to increase the reversible and decrease the irreversible capacity of carbon. Active sites on the carbon surface result in a large irreversible capacity and a second lithium insertion-release mechanism. However, this new mechanism has a short cycle life.

  19. Mesocarbon Microbead Carbon-Supported Magnesium Hydroxide Nanoparticles: Turning Spent Li-ion Battery Anode into a Highly Efficient Phosphate Adsorbent for Wastewater Treatment.

    PubMed

    Zhang, Yan; Guo, Xingming; Wu, Feng; Yao, Ying; Yuan, Yifei; Bi, Xuanxuan; Luo, Xiangyi; Shahbazian-Yassar, Reza; Zhang, Cunzhong; Amine, Khalil

    2016-08-24

    Phosphorus in water eutrophication has become a serious problem threatening the environment. However, the development of efficient adsorbents for phosphate removal from water is lagging. In this work, we recovered the waste material, graphitized carbon, from spent lithium ion batteries and modified it with nanostructured Mg(OH)2 on the surface to treat excess phosphate. This phosphate adsorbent shows one of the highest phosphate adsorption capacities to date, 588.4 mg/g (1 order of magnitude higher than previously reported carbon-based adsorbents), and exhibits decent stability. A heterogeneous multilayer adsorption mechanism was proposed on the basis of multiple adsorption results. This highly efficient adsorbent from spent Li-ion batteries displays great potential to be utilized in industry, and the mechanism study paved a way for further design of the adsorbent for phosphate adsorption. PMID:27463402

  20. Modified Mesoporous Silica (SBA–15) with Trithiane as a new effective adsorbent for mercury ions removal from aqueous environment

    PubMed Central

    2014-01-01

    Background Removal of mercury from aqueous environment has been highly regarded in recent years and different methods have been tested for this purpose. One of the most effective ways for mercury ions (Hg+2) removal is the use of modified nano porous compounds. Hence, in this work a new physical modification of mesoporous silica (SBA-15) with 1, 3, 5 (Trithiane) as modifier ligand and its application for the removal of Hg+2 from aqueous environment has been investigated. SBA-15 and Trithiane were synthesized and the presence of ligand in the silica framework was demonstrated by FTIR spectrum. The amounts of Hg+2 in the samples were determined by cold vapor generation high resolution continuum source atomic absorption spectroscopy. Also, the effects of pH, stirring time and weight of modified SBA-15 as three major parameters for effective adsorption of Hg+2 were studied. Results The important parameter for the modification of the adsorbent was Modification ratio between ligand and adsorbent in solution which was 1.5. The results showed that the best Hg+2 removal condition was achieved at pH = 5.0, stirring time 15 min and 15.0 mg of modified adsorbent. Moreover, the maximum percentage removal of Hg+2 and the capacity of adsorbent were 85% and 10.6 mg of Hg+2/g modified SBA-15, respectively. Conclusions To sum up, the present investigation introduced a new modified nano porous compound as an efficient adsorbent for removal of Hg+2 from aqueous environment. PMID:25097760

  1. Recycling of spent adsorbents for oxyanions and heavy metal ions in the production of ceramics.

    PubMed

    Verbinnen, Bram; Block, Chantal; Van Caneghem, Jo; Vandecasteele, Carlo

    2015-11-01

    Spent adsorbents for oxyanion forming elements and heavy metals are classified as hazardous materials and they are typically treated by stabilization/solidification before landfilling. The use of lime or cement for stabilization/solidification entails a high environmental impact and landfilling costs are high. This paper shows that mixing spent adsorbents in the raw material for the production of ceramic materials is a valuable alternative to stabilize oxyanion forming elements and heavy metals. The produced ceramics can be used as construction material, avoiding the high economic and environmental impact of stabilization/solidification followed by landfilling. To study the stabilization of oxyanion forming elements and heavy metals during the production process, two series of experiments were performed. In the first series of experiments, the main pollutant, Mo was adsorbed onto iron-based adsorbents, which were then mixed with industrial sludge (3 w/w%) and heated at 1100°C for 30 min. Mo was chosen, as this element is easily adsorbed onto iron-based adsorbents and it is the element that is the most difficult to stabilize (i.e. the highest temperatures need to be reached before the concentrations in the leachate are reduced). Leaching concentration from the 97/3 sludge/adsorbent mixture before heating ranged between 85 and 154 mg/kg; after the heating process they were reduced to 0.42-1.48 mg/kg. Mo was actually stabilized, as the total Mo concentration after addition was not affected by the heat treatment. In the second series of experiments, the sludge was spiked with other heavy metals and oxyanion forming elements (Cr, Ni, Cu, Zn, As, Cd and Pb) in concentrations 5 times higher than the initial concentrations; after heat treatment the leachate concentrations were below the regulatory limit values. The incorporation of spent adsorbents in ceramic materials is a valuable and sustainable alternative to the existing treatment methods, saving raw materials in the

  2. Oxygen ion response to proton bursty bulk flows

    NASA Astrophysics Data System (ADS)

    Nilsson, Hans; Hamrin, Maria; Pitkänen, Timo; Karlsson, Tomas; Slapak, Rikard; Andersson, Laila; Gunell, Herbert; Schillings, Audrey; Vaivads, Andris

    2016-08-01

    We have used Cluster spacecraft data from the years 2001 to 2005 to study how oxygen ions respond to bursty bulk flows (BBFs) as identified from proton data. We here define bursty bulk flows as periods of proton perpendicular velocities more than 100 km/s and a peak perpendicular velocity in the structure of more than 200 km/s, observed in a region with plasma beta above 1 in the near-Earth central tail region. We find that during proton BBFs only a minor increase in the O+ velocity is seen. The different behavior of the two ion species is further shown by statistics of H+ and O+ flow also outside BBFs: For perpendicular earthward velocities of H+ above about 100 km/s, the O+ perpendicular velocity is consistently lower, most commonly being a few tens of kilometers per second earthward. In summary, O+ ions in the plasma sheet experience less acceleration than H+ ions and are not fully frozen in to the magnetic field. Therefore, H+ and O+ motion is decoupled, and O+ ions have a slower earthward motion. This is particularly clear during BBFs. This may add further to the increased relative abundance of O+ ions in the plasma sheet during magnetic storms. The data indicate that O+ is typically less accelerated in association with plasma sheet X lines as compared to H+.

  3. Modeling of Transmittance Degradation Caused by Optical Surface Contamination by Atomic Oxygen Reaction with Adsorbed Silicones

    NASA Technical Reports Server (NTRS)

    Snyder, Aaron; Banks, Bruce; Miller, Sharon; Stueber, Thomas; Sechkar, Edward

    2001-01-01

    A numerical procedure is presented to calculate transmittance degradation caused by contaminant films on spacecraft surfaces produced through the interaction of orbital atomic oxygen (AO) with volatile silicones and hydrocarbons from spacecraft components. In the model, contaminant accretion is dependent on the adsorption of species, depletion reactions due to gas-surface collisions, desorption, and surface reactions between AO and silicone producing SiO(x), (where x is near 2). A detailed description of the procedure used to calculate the constituents of the contaminant layer is presented, including the equations that govern the evolution of fractional coverage by specie type. As an illustrative example of film growth, calculation results using a prototype code that calculates the evolution of surface coverage by specie type is presented and discussed. An example of the transmittance degradation caused by surface interaction of AO with deposited contaminant is presented for the case of exponentially decaying contaminant flux. These examples are performed using hypothetical values for the process parameters.

  4. Reactions of unsaturated oxygenates on rhodium(111) as probes of multiple coordination of adsorbates

    SciTech Connect

    Brown, N.F.; Barteau, M.A.

    1992-05-20

    The interactions of acrolein, CH{sub 2}=CHCHO, and allyl alcohol, CH{sub 2}=CHCH{sub 2}OH, with the Rh(111) surface are dominated at low temperatures by the oxygen function of each molecule. Acrolein is bound initially in an {eta}{sup 2}(C,O) configuration; allyl alcohol dissociates to form an allyl alkoxide. For both species, vibrational spectra show significant rehybridization of the olefinic groups upon heating to 200 K and suggest that the surface intermediates are {eta}{sup 4}(C,C,CO)-acrolein and {eta}{sup 3} (C,CO)-allyl alkoxide. Both intermediates eliminate CO between 200 and 300 K. However, like that of their aliphatic analogues, decarbonylation of acrolein and allyl alcohol does not proceed via a common pathway. Acrolein decomposes to C{sub 2}H{sub 6}, C{sub 2}H{sub 4}, CO, H{sub 2}, and surface ethylidyne intermediates, but neither allyl alcohol nor any primary alcohol examined on Rh(111) to date produces volatile hydrocarbon products. Thus, although inclusion of the C=C group in the molecules alters the stability of the corresponding surface intermediates, the divergence of reaction pathways for alcohols and aldehydes is unaffected. These results suggest that surface reaction pathways for CO insertion and elimination are considerably more complex than previously recognized. 32 refs., 9 figs., 2 tabs.

  5. Theoretical Analysis of Electrochemical Formation and Phase Transition of Oxygenated Adsorbates on Pt(111).

    PubMed

    Chen, Junxiang; Luo, Siwei; Liu, Yuwen; Chen, Shengli

    2016-08-10

    The electrochemical oxygenation processes of Pt(111) surface are investigated by combining density functional theory (DFT) calculations and Monto Carlo (MC) simulations. DFT calculations are performed to construct force-field parameters for computing the energy of (√3 × √3)R30°-structured OH*-H2O* hydrogen-bonding networks (differently dissociated water bilayer) on the Pt(111) surface, with which MC simulations are conducted to probe the reversible H2O* ↔ OH* conversion in OH*-H2O* networks. The simulated isotherm (relation between electrode potential and OH* coverage) agrees well with that predicted by the experimental cyclic voltammetry (CV) in the potential region of 0.55-0.85 V (vs RHE). It is suggested that the butterfly shape of CV in this region is due to different variation trends of Pt-H2O* distance in low and high OH* coverages. DFT calculation results indicate that the oxidative voltammetry in the potential region from 0.85 V to ca. 1.07 V is associated with the dissociation of OH* to O*, which yields surface structures consisting of OH*-H2O* networks and (√3 × √3)-structured O* clusters. The high stability of the half-dissociated water bilayer (OH*-H2O* hydrogen-bonding network with equal OH* and H2O* coverages) formed in the butterfly region makes OH* dissociation initially very difficult in energetics, but become facile once starts due to the destabilization of OH* by the formed O* nearby. This explains the experimentally observed nucleation and growth behavior of O* phase formation and the high asymmetry of oxidation-reduction voltammetry in this potential region. PMID:27377100

  6. Magnetic hydroxyapatite nanoparticles: an efficient adsorbent for the separation and removal of nitrate and nitrite ions from environmental samples.

    PubMed

    Ghasemi, Ensieh; Sillanpää, Mika

    2015-01-01

    A novel type of magnetic nanosorbent, hydroxyapatite-coated Fe2O3 nanoparticles was synthesized and used for the adsorption and removal of nitrite and nitrate ions from environmental samples. The properties of synthesized magnetic nanoparticles were characterized by scanning electron microscopy, Fourier transform infrared spectroscopy, and X-ray powder diffraction. After the adsorption process, the separation of γ-Fe2O3@hydroxyapatite nanoparticles from the aqueous solution was simply achieved by applying an external magnetic field. The effects of different variables on the adsorption efficiency were studied simultaneously using an experimental design. The variables of interest were amount of magnetic hydroxyapatite nanoparticles, sample volume, pH, stirring rate, adsorption time, and temperature. The experimental parameters were optimized using a Box-Behnken design and response surface methodology after a Plackett-Burman screening design. Under the optimum conditions, the adsorption efficiencies of magnetic hydroxyapatite nanoparticles adsorbents toward NO3(-) and NO2(-) ions (100 mg/L) were in the range of 93-101%. The results revealed that the magnetic hydroxyapatite nanoparticles adsorbent could be used as a simple, efficient, and cost-effective material for the removal of nitrate and nitrite ions from environmental water and soil samples.

  7. Removal of heavy metal ions from aqueous solution using red loess as an adsorbent.

    PubMed

    Xing, Shengtao; Zhao, Meiqing; Ma, Zichuan

    2011-01-01

    The adsorption behaviors of heavy metals onto novel low-cost adsorbent, red loess, were investigated. Red loess was characterized by X-ray diffraction, scanning electron microscopy and Fourier transform infrared spectra. The results indicated that red loess mainly consisted of silicate, ferric and aluminum oxides. Solution pH, adsorbent dosage, initial metal concentration, contact time and temperature significantly influenced the efficiency of heavy metals removal. The adsorption reached equilibrium at 4 hr, and the experimental equilibrium data were fitted to Langmuir monolayer adsorption model. The adsorption of Cu(II) and Zn(II) onto red loess was endothermic, while the adsorption of Pb(II) was exothermic. The maximum adsorption capacities of red loess for Pb(II), Cu(II) and Zn(II) were estimated to be 113.6, 34.2 and 17.5 mg/g, respectively at 25 degrees C and pH 6. The maximum removal efficiencies were 100% for Pb(II) at pH 7, 100% for Cu(II) at pH 8, and 80% for Zn(II) at pH 8. The used adsorbents were readily regenerated using dilute HCl solution, indicating that red loess has a high reusability. All the above results demonstrated that red loess could be used as a possible alternative low-cost adsorbent for the removal of heavy metals from aqueous solution.

  8. Binding of ether and carbonyl oxygens to lithium ion

    SciTech Connect

    Blint, R.J.

    1994-12-31

    The electrolyte for a lithium battery is a lithium salt (e.g. lithium Perchlorate) dissolved in an organic solvent or a mixture of organic solvents. The conductivity in these electrolytes is ionic and needs to be as high as possible to efficiently remove energy from the battery. The diffusion coefficient of the solvated ion in liquid electrolytes is inversely dependent on the radius of the salvation sphere. Consequently conductivity will increase with a decrease in the size of the salvation shell. The size of the salvation shell is determined by the size and coordination number of the solvent molecules. The types of organic solvents in electrolytes used in lithium battery applications are usually differentiated based on their perceived solvation properties. These solvents are often small, oxygen containing organic molecules which move with the Li{sup +} ions. This paper calculates the binding energies of some of these solvents to Li{sup +} using molecular quantum mechanics (MQM) techniques. The binding energies of the various solvents to Li{sup +} may determine which solvents will be preferentially bound to the ion. In liquid organic electrolytes, then, it will be the identity of the solvent and the coordination number which most affect the conductivity; the binding energies determine both of these properties. Carbonyl oxygens which occur in formaldehyde, acetaldehyde, acetone, ethylene carbonate and propylene carbonate have different Li{sup +} bonding properties than do the ether oxygens which occur in water, dimethyl ether and diethyl ether. Polymer solvents for the lithium salts such as the polyethers have chains which are too long to move with the binding energies then serve as the basis for a different Li{sup +} transport. Dimethyl ether and diethyl ether serve both as solvents and models for the polyethers.

  9. Method for providing oxygen ion vacancies in lanthanide oxides

    DOEpatents

    Kay, D. Alan R.; Wilson, William G.

    1989-12-05

    A method for desulfurization of fuel gases resulting from the incomplete combustion of sulfur containing hydrocarbons whereby the gases are treated with lanthanide oxides containing large numbers of oxygen-ion vacancies providing ionic porosity which enhances the ability of the lanthanide oxides to react more rapidly and completely with the sulfur in the fuel gases whereby the sulfur in such gases is reduced to low levels suitable for fuels for firing into boilers of power plants generating electricity with steam turbine driven generators, gas turbines, fuel cells and precursors for liquid fuels such as methanol and the like.

  10. Evaluation of a low-cost adsorbent for removal of toxic metal ions from wastewater of an electroplating factory.

    PubMed

    Sousa, Francisco W; Sousa, Marcelo James; Oliveira, Isadora R N; Oliveira, André G; Cavalcante, Rivelino M; Fechine, Pierre B A; Neto, Vicente O S; de Keukeleire, Denis; Nascimento, Ronaldo F

    2009-08-01

    In this study, sugar cane residue or bagasse was used for removal of toxic metal ions from wastewater of an electroplating factory located in northeast Brazil. Prior acid treatment increased the adsorption efficacies in batch wise experiments. The microstructure of the material before and after the treatment was investigated by X-ray diffraction, infrared spectroscopy and scanning electron microscopy. Column operations showed that removals of Cu(2+), Ni(2+) and Zn(2+) from wastewater (in the absence of cyanide) were 95.5%, 96.3.0%, and 97.1%, respectively. Regeneration of the adsorbent obtained in acid indicated that the efficiencies decreased only after the fourth cycle of re-use. Acid-treated sugar cane bagasse can be considered a viable alternative to common methods to remove toxic metal ions from aqueous effluents of electroplating industries.

  11. Coupled, Nitrogen, Oxygen, Carbon and Ion Chemistry on Titan

    NASA Astrophysics Data System (ADS)

    Yelle, Roger; Vuitton, Veronique; Lavvas, Panayotis; Klippenstein, Stephen; Horst, Sarah

    2016-06-01

    We present simulations of the coupled nitrogen, oxygen, and ion chemistry on Titan using a state-of-the-art photochemical model. The model is one dimensional and extends from the surface to the exobase. The chemistry linking 160 neutral species and 172 ion species is described through networks including 1139 neutral reactions and 4361 ion reactions. UV photolysis of 59 species is included as well as dissociation and ionization of 16 species due to suprathermal electrons. Reaction rate coefficients are obtained from a thorough review of the literature supplemented by calculations of rates of important reactions when laboratory values are not available. Comparison of the model with available observational constraints helps to determine the fundamental chemical pathways in the atmosphere. We will discuss in particular the importance of recent measurements of HNC, HC15N, CO2, and H2O and the role of ion chemistry in the synthesis of neutral species. Key reactions that require further laboratory of theoretical study will be identified.

  12. Viral clearance by flow-through mode ion exchange columns and membrane adsorbers.

    PubMed

    Miesegaes, G R; Lute, S C; Read, E K; Brorson, K A

    2014-01-01

    Anion exchange (AEX) is a common downstream purification operation for biotechnology products manufactured in cell culture such as therapeutic monoclonal antibodies (mAbs) and Fc-fusion proteins. We present a head-to-head comparison of the viral clearance efficiency of AEX adsorbers and column chromatography using the same process fluids and comparable run conditions. We also present overall trends from the CDER viral clearance database. In our comparison of multiple brands of resins and adsorbers, clearance of three model viruses (PPV, X-MuLV, and PR772) was largely comparable, with some exceptions which may reflect run conditions that had not been optimized on a resin/membrane specific basis.

  13. Biosorption of metal ions using a low cost modified adsorbent (Mauritia flexuosa): experimental design and mathematical modeling.

    PubMed

    Melo, Diego de Quadros; Vidal, Carla Bastos; Medeiros, Thiago Coutinho; Raulino, Giselle Santiago Cabral; Dervanoski, Adriana; Pinheiro, Márcio do Carmo; Nascimento, Ronaldo Ferreira do

    2016-09-01

    Buriti fibers were subjected to an alkaline pre-treatment and tested as an adsorbent to investigate the adsorption of copper, cadmium, lead and nickel in mono- and multi-element aqueous solutions, the results showed an increase in the adsorption capacity compared to the unmodified Buriti fiber. The effects of pH, adsorbent mass, agitation rate and initial metal ions concentration on the efficiency of the adsorption process were studied using a fractional 2(4-1) factorial design, and the results showed that all four parameters influenced metal adsorption differently. Fourier transform infrared spectrometry and X-ray fluorescence analysis were used to identify the groups that participated in the adsorption process and suggest its mechanisms and they indicated the probable mechanisms involved in the adsorption process are mainly ion exchange. Kinetic and thermodynamic equilibrium parameters were determined. The adsorption kinetics were adjusted to the homogeneous diffusion model. The adsorption equilibrium was reached in 30 min for Cu(2+) and Pb(2+), 20 min for Ni(2+) and instantaneously for Cd(2+). The results showed a significant difference was found in the competitiveness for the adsorption sites. A mathematical model was used to simulate the breakthrough curves in multi-element column adsorption considering the influences of external mass transfer and intraparticle diffusion resistance.

  14. Polypyrrole/cobalt ferrite/multiwalled carbon nanotubes as an adsorbent for removing uranium ions from aqueous solutions.

    PubMed

    Liu, Qi; Zhu, Jiahui; Tan, Lichao; Jing, Xiaoyan; Liu, Jingyuan; Song, Dalei; Zhang, Hongsen; Li, Rumin; Emelchenko, G A; Wang, Jun

    2016-05-31

    A novel rod-like, dual-shell structural adsorbent of polypyrrole/cobalt ferrite/multiwalled carbon nanotubes (PPy/CoFe2O4/MWCNTs) was successfully synthesized by a hydrothermal method, which could easily separate uranium(vi) ions with an external magnetic field. The structure and morphology of PPy/CoFe2O4/MWCNTs were characterized by VSM, XRD, XPS TEM and FT-IR. The results proved that the dual-shell structure was obtained in which a shell of cobalt ferrite and polypyrrole formed around the MWCNTs core. In batch adsorption experiments, including pH, equilibrium time and temperature on uranium adsorption, were investigated. The main results show that the PPy/CoFe2O4/MWCNTs composite has a higher affinity towards the uptake of uranium(vi) from aqueous solutions. The highest adsorption capacity reached was 148.8 mg U per g at pH 7. A kinetic analysis showed that the adsorption process was best described by a pseudo-second-order kinetic model. The uranium sorption equilibrium data correlated well with the Langmuir sorption isotherm model in the thermodynamic analysis. 0.5 mol per L NaHCO3 was used as the desorbent and good adsorption properties were shown after the desorption procedures were repeated three times. Thus, PPy/CoFe2O4/MWCNTs was an excellent adsorbent for removing uranium(vi) ions. PMID:27169495

  15. Polypyrrole/cobalt ferrite/multiwalled carbon nanotubes as an adsorbent for removing uranium ions from aqueous solutions.

    PubMed

    Liu, Qi; Zhu, Jiahui; Tan, Lichao; Jing, Xiaoyan; Liu, Jingyuan; Song, Dalei; Zhang, Hongsen; Li, Rumin; Emelchenko, G A; Wang, Jun

    2016-05-31

    A novel rod-like, dual-shell structural adsorbent of polypyrrole/cobalt ferrite/multiwalled carbon nanotubes (PPy/CoFe2O4/MWCNTs) was successfully synthesized by a hydrothermal method, which could easily separate uranium(vi) ions with an external magnetic field. The structure and morphology of PPy/CoFe2O4/MWCNTs were characterized by VSM, XRD, XPS TEM and FT-IR. The results proved that the dual-shell structure was obtained in which a shell of cobalt ferrite and polypyrrole formed around the MWCNTs core. In batch adsorption experiments, including pH, equilibrium time and temperature on uranium adsorption, were investigated. The main results show that the PPy/CoFe2O4/MWCNTs composite has a higher affinity towards the uptake of uranium(vi) from aqueous solutions. The highest adsorption capacity reached was 148.8 mg U per g at pH 7. A kinetic analysis showed that the adsorption process was best described by a pseudo-second-order kinetic model. The uranium sorption equilibrium data correlated well with the Langmuir sorption isotherm model in the thermodynamic analysis. 0.5 mol per L NaHCO3 was used as the desorbent and good adsorption properties were shown after the desorption procedures were repeated three times. Thus, PPy/CoFe2O4/MWCNTs was an excellent adsorbent for removing uranium(vi) ions.

  16. Influence of carboxylic ion-pairing reagents on retention of peptides in thin-layer chromatography systems with C18 silica-based adsorbents.

    PubMed

    Gwarda, Radosław Ł; Aletańska-Kozak, Monika; Klimek-Turek, Anna; Ziajko-Jankowska, Agnieszka; Matosiuk, Dariusz; Dzido, Tadeusz H

    2016-04-01

    One of the main problems related to chromatography of peptides concerns adverse interactions of their strong basic groups with free silanol groups of the silica based stationary phase. Influence of type and concentration of ion-pairing regents on peptide retention in reversed-phase high-performance liquid chromatography (RP-HPLC) systems has been discussed before. Here we present influence of these mobile phase additives on retention of some peptide standards in high-performance thin-layer chromatography (HPTLC) systems with C18 silica-based adsorbents. We prove, that due to different characteristic of adsorbents used in both techniques (RP HPLC and HPTLC), influence of ion-pairing reagents on retention of basic and/or amphoteric compounds also may be quite different. C18 silica-based HPTLC adsorbents provide more complex mechanism of retention and should be rather considered as mixed-mode adsorbents.

  17. Effect of activated carbon surface oxygen- and/or nitrogen-containing groups on adsorption of copper(II) ions from aqueous solution

    SciTech Connect

    Biniak, S.; Pakula, M.; Szymanski, G.S.; Swiatkowski, A.

    1999-08-31

    The adsorption properties of a modified activated carbon with various oxygen-and/or nitrogen-containing surface groups toward copper ions was studied. Previously de-ashed and chemically modified commercial activated carbon D-43/1 (carbo-Tech, Essen, Germany) was used. The chemical properties of the modified carbon surface were estimated by standard neutralization titration with HCl, NaOH, and HaOC{sub 2}{sub 5}. The adsorption of Cu{sup 2+} ions on three modified activated carbons from aqueous CuSO{sub 4} solution of various pH was measured. The carbon samples with adsorbed Cu{sup 2+} ions were analyzed by spectroscopic methods (X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy). In addition, an electrochemical measurement (cyclic voltammetry) was performed using powdered activated carbon electrodes. While the modification procedures employed alter the surface only slightly, they strongly influence the surface chemical structure. Basic groups are predominant in the heat-treated samples; acidic functional groups are predominant in the oxidized sample. Both the copper cation adsorption studies and the spectral and electrochemical measurements show that adsorbed ions interact with the carbon surface in different ways. The number of adsorbed ions depends on the nature and quantity of surface acid-base functionalities and on the pH equilibrium in the aqueous solution. The possible mechanisms of interactions between metal ions and carbon surface functionalities are summarized and discussed.

  18. Reduction of electron accumulation at InN(0001) surfaces via saturation of surface states by potassium and oxygen as donor- or acceptor-type adsorbates

    SciTech Connect

    Eisenhardt, A.; Reiß, S.; Krischok, S. Himmerlich, M.

    2014-01-28

    The influence of selected donor- and acceptor-type adsorbates on the electronic properties of InN(0001) surfaces is investigated implementing in-situ photoelectron spectroscopy. The changes in work function, surface band alignment, and chemical bond configurations are characterized during deposition of potassium and exposure to oxygen. Although an expected opponent charge transfer characteristic is observed with potassium donating its free electron to InN, while dissociated oxygen species extract partial charge from the substrate, a reduction of the surface electron accumulation occurs in both cases. This observation can be explained by adsorbate-induced saturation of free dangling bonds at the InN resulting in the disappearance of surface states, which initially pin the Fermi level and induce downward band bending.

  19. Acid-base interactions and complex formation while recovering copper(II) ions from aqueous solutions using cellulose adsorbent in the presence of polyvinylpyrrolidone

    NASA Astrophysics Data System (ADS)

    Nikiforova, T. E.; Kozlov, V. A.; Islyaikin, M. K.

    2012-12-01

    The sorption properties of nontreated cotton cellulose and cellulose modified with polyvinylpyrrolidone with respect to copper(II) ions are investigated. It is established that modified cellulose adsorbents have high sorption capability associated with the formation of new sorption centers during treatment with nitrogen-containing polymer. A mechanism is proposed for acid-base interactions in aqueous solutions of acids, bases, and salts during copper(II) cation recovery using cellulose adsorbent with the participation of polyvinylpyrrolidone.

  20. Theory for charge states of energetic oxygen ions in the earth's radiation belts

    NASA Technical Reports Server (NTRS)

    Spjeldvik, W. N.; Fritz, T. A.

    1978-01-01

    Fluxes of geomagnetically trapped energetic oxygen ions have been studied in detail. Ion distributions in radial locations below the geostationary orbit, energy spectra between 1 keV and 100 MeV, and the distribution over charge states have been computed for equatorially mirroring ions. Both ionospheric and solar wind oxygen ion sources have been considered, and it is found that the charge state distributions in the interior of the radiation belts are largely independent of the charge state characteristics of the sources. In the MeV range, oxygen ions prove to be a more sensitive probe for radiation belt dynamics than helium ions and protons.

  1. "False" cytotoxicity of ions-adsorbing hydroxyapatite - Corrected method of cytotoxicity evaluation for ceramics of high specific surface area.

    PubMed

    Klimek, Katarzyna; Belcarz, Anna; Pazik, Robert; Sobierajska, Paulina; Han, Tomasz; Wiglusz, Rafal J; Ginalska, Grazyna

    2016-08-01

    An assessment of biomaterial cytotoxicity is a prerequisite for evaluation of its clinical potential. A material is considered toxic while the cell viability decreases under 70% of the control. However, extracts of certain materials are likely to reduce the cell viability due to the intense ions adsorption from culture medium (e.g. highly bioactive ceramics of high surface area). Thus, the standard ISO 10993-5 procedure is inappropriate for cytotoxicity evaluation of ceramics of high specific surface area because biomaterial extract obtained in this method (ions-depleted medium) is not optimal for cell cultures per se. Therefore, a simple test was designed as an alternative to ISO 10993-5 standard for cytotoxicity evaluation of the biomaterials of high surface area and high ions absorption capacity. The method, presented in this paper, included the evaluation of ceramics extract prepared according to corrected procedure. The corrected extract was found not cytotoxic (cell viability above 70%), suggesting that modified method for cytotoxicity evaluation of ions-adsorbing ceramics is more appropriate than ISO 10993-5 standard. For such biomaterials, the term "false" cytotoxicity is more suitable. Moreover, it was noted that NRU assay and microscopic observations should be recommended for cytotoxicity evaluation of ceramics of high surface area. PMID:27157729

  2. "False" cytotoxicity of ions-adsorbing hydroxyapatite - Corrected method of cytotoxicity evaluation for ceramics of high specific surface area.

    PubMed

    Klimek, Katarzyna; Belcarz, Anna; Pazik, Robert; Sobierajska, Paulina; Han, Tomasz; Wiglusz, Rafal J; Ginalska, Grazyna

    2016-08-01

    An assessment of biomaterial cytotoxicity is a prerequisite for evaluation of its clinical potential. A material is considered toxic while the cell viability decreases under 70% of the control. However, extracts of certain materials are likely to reduce the cell viability due to the intense ions adsorption from culture medium (e.g. highly bioactive ceramics of high surface area). Thus, the standard ISO 10993-5 procedure is inappropriate for cytotoxicity evaluation of ceramics of high specific surface area because biomaterial extract obtained in this method (ions-depleted medium) is not optimal for cell cultures per se. Therefore, a simple test was designed as an alternative to ISO 10993-5 standard for cytotoxicity evaluation of the biomaterials of high surface area and high ions absorption capacity. The method, presented in this paper, included the evaluation of ceramics extract prepared according to corrected procedure. The corrected extract was found not cytotoxic (cell viability above 70%), suggesting that modified method for cytotoxicity evaluation of ions-adsorbing ceramics is more appropriate than ISO 10993-5 standard. For such biomaterials, the term "false" cytotoxicity is more suitable. Moreover, it was noted that NRU assay and microscopic observations should be recommended for cytotoxicity evaluation of ceramics of high surface area.

  3. Role of Cu-Ion Doping in Cu-α-MnO2 Nanowire Electrocatalysts for the Oxygen Reduction Reaction

    DOE PAGES

    Davis, Danae J.; Lambert, Timothy N.; Vigil, Julian A.; Rodriguez, Mark A.; Brumbach, Michael T.; Coker, Eric N.; Limmer, Steven J.

    2014-07-09

    The role of Cu-ion doping in α-MnO2 electrocatalysts for the oxygen reduction reaction in alkaline electrolyte was investigated. Copper doped α-MnO2 nanowires (Cu-α-MnO2) were prepared with varying amounts of Cu2+ using a solvothermal method. The electrocatalytic dataindicates that Cu-α-MnO2 nanowires have higher terminal current densities, enhanced kinetic rate constants, and improved charge transfer resistances that trend with Cu-content, exceeding values attained by α-MnO2 alone. The observed improvement in catalytic behavior correlates with an increase in Mn3+ content for the Cu-α-MnO2 nanowires. The Mn3+/Mn4+ couple is themediator for the rate-limiting redox driven O2-/OH- exchange. It is proposed that O2 adsorbs viaanmore » axial site (the eg orbital on the Mn3+ d4 ion) at the surface, or at edge defects, of the nanowireand that the increase in covalent nature of the nanowire with Cu-ion doping leads to stabilization of O2 adsorbates and faster rates of reduction. This work is applicable to other manganese oxide electrocatalysts and shows for the first time there is a correlation for manganese oxides between electrocatalytic activity for the ORR in alkaline electrolyte and an increase in Mn3+ character of the oxide.« less

  4. Quantitative secondary ion mass spectrometric analysis of secondary ion polarity in GaN films implanted with oxygen

    NASA Astrophysics Data System (ADS)

    Hashiguchi, Minako; Sakaguchi, Isao; Adachi, Yutaka; Ohashi, Naoki

    2016-10-01

    Quantitative analyses of N and O ions in GaN thin films implanted with oxygen ions (16O+) were conducted by secondary ion mass spectrometry (SIMS). Positive (CsM+) and negative secondary ions extracted by Cs+ primary ion bombardment were analyzed for oxygen quantitative analysis. The oxygen depth profiles were obtained using two types of primary ion beams: a Gaussian-type beam and a broad spot beam. The oxygen peak concentrations in GaN samples were from 3.2 × 1019 to 7.0 × 1021 atoms/cm3. The depth profiles show equivalent depth resolutions in the two analyses. The intensity of negative oxygen ions was approximately two orders of magnitude higher than that of positive ions. In contrast, the O/N intensity ratio measured using CsM+ molecular ions was close to the calculated atomic density ratio, indicating that the SIMS depth profiling using CsM+ ions is much more effective for the measurements of O and N ions in heavy O-implanted GaN than that using negative ions.

  5. High-productivity membrane adsorbers: Polymer surface-modification studies for ion-exchange and affinity bioseparations

    NASA Astrophysics Data System (ADS)

    Chenette, Heather C. S.

    membrane adsorbers were found to have a static binding capacity for con A (6.0 mg/mL) that is nearly the same as the typical dextran-based separation media used in practice. Binding under dynamic conditions was tested using flow rates of 0.1-1.0 mL/min. No bound lectin was observed for the higher flow rate. The first Damkohler number was used to assess whether adsorption kinetics or mass transport contributed the limitation to conA binding. Analyses indicate that this system is not limited by the accessibility of the binding sites, but by the inherently low rate of adsorption of conA onto the glycopolymer. The research described in Chapter 4 focuses on reaction chemistry experiments to incorporate a phosphonate-based polymer in the membrane platform to develop a new class of affinity adsorbers that function based on their affinity for Arginine (Arg) amino acid residues. The hypothesis was that benzyl phosphonate-containing functional polymers would form strong complexes with Arg-rich proteins as a result of multivalent binding. Introducing a new class of affinity membranes for purification of Arg-rich and Arg-tagged proteins may have an impact similar to the introduction of immobilized metal ion affinity chromatography (IMAC), which would be a significant achievement. Using Arg-tags would overcome some of the associated drawbacks of using metal ions in IMAC. Additionally, some cell penetrating peptides are said to be Arg-rich, and this would be a convenient feature to exploit for their isolation and purification. Lysozyme was used as a model Arg-rich protein. The affinity membranes show a static binding capacity of 3 mg/mL. (Abstract shortened by UMI.)

  6. Neutral atomic oxygen beam produced by ion charge exchange for Low Earth Orbital (LEO) simulation

    NASA Technical Reports Server (NTRS)

    Banks, Bruce; Rutledge, Sharon; Brdar, Marko; Olen, Carl; Stidham, Curt

    1987-01-01

    A low energy neutral atomic oxygen beam system was designed and is currently being assembled at the Lewis Research Center. The system utilizes a 15 cm diameter Kaufman ion source to produce positive oxygen ions which are charge exchange neutralized to produce low energy (variable from 5 to 150 eV) oxygen atoms at a flux simulating real time low Earth orbital conditions. An electromagnet is used to direct only the singly charged oxygen ions from the ion source into the charge exchange cell. A retarding potential grid is used to slow down the oxygen ions to desired energies prior to their charge exchange. Cryogenically cooled diatomic oxygen gas in the charge exchange cell is then used to transfer charge to the oxygen ions to produce a neutral atomic oxygen beam. Remaining non-charge exchanged oxygen ions are then swept from the beam by electromagnetic or electrostatic deflection depending upon the desired experiment configuration. The resulting neutral oxygen beam of 5 to 10 cm in diameter impinges upon target materials within a sample holder fixture that can also provide for simultaneous heating and UV exposure during the atomic oxygen bombardment.

  7. Electronic States of Oxygen Ions of Molten Slags Used for Iron and Steel Making

    NASA Astrophysics Data System (ADS)

    Morishita, Masao; Koyama, Koichiro; Hatamoto, Akinori; Morinaga, Masahiko; Adachi, Hirohiko

    Regarding molten slags used for iron and steel making, discrete anion models, SiO44- and Si2O6-, coordinating metal ions such as Na+, K+, Ca2+ and Mg2+ were examined by the DV-X[alpha] method. The bond order which is a measure of the covalent bond and the ionicity which is a measure of the charge transfer were calculated. The bond orders between the Si ions and non-bridging oxygen ions were found to be very high. On the other hand, the bond orders between the Si ions and the oxygen ions coordinating the metal ions were very low, that is, the covalent bonds between them are weak. The metal ions such as Na+, K+, Ca2+ and Mg2+ are necessary for the formation of the free oxygen ions as well as the decomposition of polymerized structures. As a result, the bond orders between the Si ions and the oxygen ions coordinating the metal ions were found to be correlated with reactivity such as sulphide capacity of molten slags. The values of ionicity of the non-bridging oxygen ions were -1.0~-1.4. These values of non-bridging oxygen ions are approximately equal to the valences obtained from the statistical thermodynamics studies.

  8. New heterocycle modified chitosan adsorbent for metal ions (II) removal from aqueous systems.

    PubMed

    Kandile, Nadia G; Mohamed, Hemat M; Mohamed, Mansoura I

    2015-01-01

    A new hydrogel based on a modified chitosan CS-B was synthesized and evaluated for its metal ion removal from aqueous systems. The CS-B hydrogel was prepared through modification of chitosan with 4-((1, 3-dioxoisoindolin-2-ylimino) methyl) benzaldehyde as a heterocyclic component. The new hydrogel was analyzed by diverse techniques such as FTIR, XRD, TGA, SEM, and swelling tests. The adsorption capacity of CS-B for metal ions Co(2+), Hg(2+), Cu(2+), Zn(2+), and Pb(2+) from aqueous systems at different pH values showed various levels of efficiency. The metal ion uptake data over a range of pH values for Co(2+) and Hg(2+) showed the highest adsorption capacity while Cu(2+), Zn(2+), and Pb(2+) showed moderate adsorption capacity. Selective metal ion efficiency was highest for Co(2+) and lowest for Hg(2+) in their binary mixture.

  9. Molecular orientation of molybdate ions adsorbed on goethite nanoparticles revealed by polarized in situ ATR-IR spectroscopy

    NASA Astrophysics Data System (ADS)

    Davantès, Athénaïs; Lefèvre, Grégory

    2016-11-01

    The speciation of species adsorbed on nanoparticles is a major concern for several fields, as environmental pollution and remediation, surface functionalization, or catalysis. Attenuated total reflectance infrared spectroscopy (ATR-IR) was amongst the rare methods able to give in situ information about the geometry of surface complexes on nanoparticles. A new possibility using this technique is illustrated here with the MoO42 -/goethite system. Using deuterated goethite to avoid spectral interferences, adsorption of molybdate ions on a spontaneous oriented film of nanoparticles has been followed using a polarized infrared beam. From the decomposition of spectra in the x, y and z directions, a monodentate surface complex on the {101} faces has been found as the most probable geometry. This result demonstrates that polarized ATR-IR allows to characterize in more details adsorption mode at the atomic scale, in comparison with usual ATR-IR spectroscopy.

  10. An effective and recyclable adsorbent for the removal of heavy metal ions from aqueous system: Magnetic chitosan/cellulose microspheres.

    PubMed

    Luo, Xiaogang; Zeng, Jian; Liu, Shilin; Zhang, Lina

    2015-10-01

    Development of highly cost-effective, highly operation-convenient and highly efficient natural polymer-based adsorbents for their biodegradability and biocompatibility, and supply of safe drinking water are the most threatening problems in water treatment field. To tackle the challenges, a new kind of efficient recyclable magnetic chitosan/cellulose hybrid microspheres was prepared by sol-gel method. By embedding magnetic γ-Fe2O3 nanoparticles in chitosan/cellulose matrix drops in NaOH/urea aqueous solution, it combined renewability and biocompatibility of chitosan and cellulose as well as magnetic properties of γ-Fe2O3 to create a hybrid system in heavy metal ions removal.

  11. Enhancement of Sodium Ion Battery Performance Enabled by Oxygen Vacancies.

    PubMed

    Xu, Yang; Zhou, Min; Wang, Xin; Wang, Chengliang; Liang, Liying; Grote, Fabian; Wu, Minghong; Mi, Yan; Lei, Yong

    2015-07-20

    The utilization of oxygen vacancies (OVs) in sodium ion batteries (SIBs) is expected to enhance performance, but as yet it has rarely been reported. Taking the MoO(3-x) nanosheet anode as an example, for the first time we demonstrate the benefits of OVs on SIB performance. Moreover, the benefits at deep-discharge conditions can be further promoted by an ultrathin Al2O3 coating. A series of measurements show that the OVs increase the electric conductivity and Na-ion diffusion coefficient, and the promotion from ultrathin coating lies in the effective reduction of cycling-induced solid-electrolyte interphase. The coated nanosheets exhibited high reversible capacity and great rate capability with the capacities of 283.9 (50 mA g(-1)) and 179.3 mAh g(-1) (1 A g(-1)) after 100 cycles. This work may not only arouse future attention on OVs for sodium energy storage, but also open up new possibilities for designing strategies to utilize defects in other energy storage systems.

  12. Do Ca2+-adsorbing ceramics reduce the release of calcium ions from gypsum-based biomaterials?

    PubMed

    Belcarz, Anna; Zalewska, Justyna; Pałka, Krzysztof; Hajnos, Mieczysław; Ginalska, Grazyna

    2015-02-01

    Bone implantable materials based on calcium sulfate dihydrate dissolve quickly in tissue liquids and release calcium ions at very high levels. This phenomenon induces temporary toxicity for osteoblasts, may cause local inflammation and delay the healing process. Reduction in the calcium ion release rate by gypsum could be therefore beneficial for the healing of gypsum-filled bone defects. The aim of this study concerned the potential use of calcium phosphate ceramics of various porosities for the reduction of high Ca(2+) ion release from gypsum-based materials. Highly porous ceramics failed to reduce the level of Ca(2+) ions released to the medium in a continuous flow system. However, it succeeded to shorten the period of high calcium level. It was not the phase composition but the high porosity of ceramics that was found crucial for both the shortening of the Ca(2+) release-related toxicity period and intensification of apatite deposition on the composite. Nonporous ceramics was completely ineffective for this purpose and did not show any ability to absorb calcium ions at a significant level. Moreover, according to our observations, complex studies imitating in vivo systems, rather than standard tests, are essential for the proper evaluation of implantable biomaterials. PMID:25492196

  13. Do Ca2+-adsorbing ceramics reduce the release of calcium ions from gypsum-based biomaterials?

    PubMed

    Belcarz, Anna; Zalewska, Justyna; Pałka, Krzysztof; Hajnos, Mieczysław; Ginalska, Grazyna

    2015-02-01

    Bone implantable materials based on calcium sulfate dihydrate dissolve quickly in tissue liquids and release calcium ions at very high levels. This phenomenon induces temporary toxicity for osteoblasts, may cause local inflammation and delay the healing process. Reduction in the calcium ion release rate by gypsum could be therefore beneficial for the healing of gypsum-filled bone defects. The aim of this study concerned the potential use of calcium phosphate ceramics of various porosities for the reduction of high Ca(2+) ion release from gypsum-based materials. Highly porous ceramics failed to reduce the level of Ca(2+) ions released to the medium in a continuous flow system. However, it succeeded to shorten the period of high calcium level. It was not the phase composition but the high porosity of ceramics that was found crucial for both the shortening of the Ca(2+) release-related toxicity period and intensification of apatite deposition on the composite. Nonporous ceramics was completely ineffective for this purpose and did not show any ability to absorb calcium ions at a significant level. Moreover, according to our observations, complex studies imitating in vivo systems, rather than standard tests, are essential for the proper evaluation of implantable biomaterials.

  14. Lignocellulosic Wheat Straw-Derived Ion-Exchange Adsorbent for Heavy Metals Removal.

    PubMed

    Krishnani, K K

    2016-02-01

    The aim of this work is to develop partially delignified Ca(2+)-and-Mg(2+)-ion-exchanged product from lignocellulosic wheat straw for the removal of eight different heavy metals Pb(2+), Cd(2+), Hg(2+), Co(2+), Ni(2+), Mn(2+), Zn(2+), and Cu(2+) and for detoxification of Cr(VI). Maximum fixation capacity, pH, and initial metal concentration dependence were determined to confirm strong affinity of Pb(2+), Cd(2+), Cu(2+), Zn(2+), and Hg(2+) ions onto the product, whereas Co(2+), Ni(2+), and Mn(2+) were the least fixed. Morphology of the product characterized by scanning electron microscope showed its physical integrity. Different experimental approaches were applied to determine the role of cations such as Ca(2+), Mg(2+), and Na(+) and several functional groups present in the product in an ion exchange for the fixation of metal ions. Potentiometric titration and Scatchard and Dahlquist interpretation were employed for determination of binding site heterogeneity. Results showed strong and weak binding sites in the product. This product has advantages over other conventional processes by virtue of abundance, easy operational process, and cost reduction in waste disposal of its raw material.

  15. Cleaning Water Contaminated with Heavy Metal Ions Using Pyrolyzed Biochar Adsorbents

    EPA Science Inventory

    The extraction of pollutants from water using activated biochar materials is a low cost, sustainable approach for providing safe water in developing countries. The adsorption of copper ions, Cu (II), onto banana peels that were dried, pyrolyzed and activated was studied and compa...

  16. Removal of heavy metal ions from water by using calcined phosphate as a new adsorbent.

    PubMed

    Aklil, A; Mouflih, M; Sebti, S

    2004-08-30

    Calcined phosphate (CP) has been employed in our laboratories as a heterogeneous catalyst in a variety of reactions. In this study, CP was evaluated as a new product for removal of heavy metals from aqueous solution. Removal of Pb2+, Cu2+, and Zn2+ on the CP was investigated in batch experiments. The kinetic of lead on CP adsorption efficiency and adsorption process were evaluated and analysed using the theories of Langmuir and Freundlich. The influence of pH was studied. The adsorption capacity obtained at pH 5 were 85.6, 29.8, and 20.6 mg g(-1) for Pb2+, Cu2+ and Zn2+, respectively. We hypothesize at pH 2 and 3, the dissolution of CP and precipitation of a fluoropyromorphite for lead and the formation of solid-solution type fluorapatite for copper. The results obtained show that CP is a good adsorbent for these toxic heavy metals. The abundance of natural phosphate, its low price and non-aggressive nature towards the environment are advantage for its utilisation in point of view of wastewater and wastes clean up.

  17. The reaction of atomic oxygen with Si(100) and Si(111). II. Adsorption, passive oxidation and the effect of coincident ion bombardment

    NASA Astrophysics Data System (ADS)

    Engstrom, J. R.; Bonser, D. J.; Engel, Thomas

    The reactions of atomic oxygen with the (100) and (111) surfaces of silicon have been investigated by employing supersonic molecular beam techniques, X-ray photoelectron spectroscopy (XPS), and low-energy ion scattering spectroscopy (ISS). Atomic oxygen adsorbs with unit probability on the clean silicon surface, independent of substrate temperature (110-800 K) and incident mean translational energy (3-16 kcal mol -1). Oxidation of clean silicon with an oxygen atom beam is characterized by wo stages: a "fast" stage that corresponds to oxygen chemisorption in the topmost 2-3 silicon layers; and a "slow" stage that corresponds to oxygen incorporation and oxide film growth. The chemisorption stage is described by first-order Langmuirian kinetics with an apparent saturation coverage of approximately 4 ML O(a), the oxide growth stage by lddirect" logarithmic kinetics, where d x/d t = α exp(- x/ L), where x is the oxide thickness. Observation of significant oxidation at substrate temperatures of 110 K suggests that oxie growth in the slow stage may occur bya field-assisted mechanism, where an internal electric field aids transport of oxygen to the underlying silicon substrate layers. XPS and ISS results support a two-dimensional layer-by-layer growth mechanism for oxidation at substrate temperatures below 900 K. At higher temperatures, T ≥ 1050 K, oxide growth is three-dimensional involving nucleation and growth of bulk-like oxide islands even for mean coverages as low as 3 ML O(a). ISS results lend support to the formation of "on-top" adsorbed oxygen atoms that cap silicon dangling bonds at the oxide/gas interface. Coincident bombardment of the silicon substrate with an Ar - ion beam leads to an enhanced rate of oxidation. The enhancement can be understood in terms of a model involving secondary implantation of adsorbed oxygen atoms, coupled with the simultaneous formation of reactive sites (e.g., dangling bonds, vacancies) for oxygen chemisorption. The effect of

  18. Assessing ligand selectivity for uranium over vanadium ions to aid in the discovery of superior adsorbents for extraction of UO2(2+) from seawater.

    PubMed

    Ivanov, Alexander S; Bryantsev, Vyacheslav S

    2016-06-28

    Uranium is used as the basic fuel for nuclear power plants, which generate significant amounts of electricity and have life cycle carbon emissions that are as low as renewable energy sources. However, the extraction of this valuable energy commodity from the ground remains controversial, mainly because of environmental and health impacts. Alternatively, seawater offers an enormous uranium resource that may be tapped at minimal environmental cost. Nowadays, amidoxime polymers are the most widely utilized sorbent materials for large-scale extraction of uranium from seawater, but they are not perfectly selective for uranyl, UO2(2+). In particular, the competition between UO2(2+) and VO(2+)/VO2(+) cations poses a significant challenge to the efficient mining of UO2(2+). Thus, screening and rational design of more selective ligands must be accomplished. One of the key components in achieving this goal is the establishment of computational techniques capable of assessing ligand selectivity trends. Here, we report an approach based on quantum chemical calculations that achieves high accuracy in reproducing experimental aqueous stability constants for VO(2+)/VO2(+) complexes with ten different oxygen donor ligands. The predictive power of the developed computational protocol is demonstrated for amidoxime-type ligands, providing greater insights into new design strategies for the development of the next generation of adsorbents with high selectivity toward UO2(2+) over VO(2+)/VO2(+) ions. Importantly, the results of calculations suggest that alkylation of amidoxime moieties present in poly(acrylamidoxime) sorbents can be a potential route to better discrimination between the uranyl and competing vanadium ions in seawater. PMID:27285397

  19. Cathodic reduction of oxygen and hydrogen peroxide at cobalt and iron crowned phthalocyanines adsorbed on highly oriented pyrolytic graphite electrodes

    SciTech Connect

    Kobayashi, N.; Janda, P.; Lever, A.B.P. )

    1992-12-09

    The surface electrochemistry of iron and cobalt crowned phthalocyanine (Fe[sup II]CRPc(-2) and Co[sup II]CRPc(-2)) adsorbed on a highly oriented pyrolytic graphite (HOPG) electrode has been explored under an argon atmosphere. The redox processes of surface bound Co[sup II]CRPc(-2)/[Co[sup I]CRPc(-2)][sup [minus

  20. Characterization of Cross-Linked Cellulosic Ion-Exchange Adsorbents: 1. Structural Properties

    PubMed Central

    Angelo, James M.; Cvetkovic, Aleksandar; Gantier, Rene; Lenhoff, Abraham M.

    2014-01-01

    The structural characteristics of the HyperCel family of cellulosic ion-exchange materials (Pall Corporation) were assessed using methods to gauge the pore dimensions and the effect of ionic strength on intraparticle architecture. Inverse size exclusion chromatography (ISEC) was applied to the S and STAR AX HyperCel derivatives. The theoretical analysis yielded an average pore radius for each material of about 5 nm, with a particularly narrow pore-size distribution. Electron microscopy techniques were used to visualize the particle structure and relate it to macroscopic experimental data. Microscopy of Q and STAR AX HyperCel anion exchangers presented some qualitative differences in pore structure that can be attributed to the derivatization using conventional quaternary ammonium and salt-tolerant ligands, respectively. Finally, the effect of ionic strength was studied through the use of salt breakthrough experiments to determine to what extent Donnan exclusion plays a role in restricting the accessible pore volume for small ions. It was determined that Donnan effects were prevalent at total ionic strengths (TIS) less than 150 mM, suggesting the presence of a ligand-containing partitioning volume within the pore space. PMID:24188996

  1. Probing the photochemistry of chemisorbed oxygen on TiO2(110) with Kr and other co-adsorbates

    SciTech Connect

    Petrik, Nikolay G.; Kimmel, Gregory A.

    2014-02-14

    Weakly bound (physisorbed) atoms and molecules such as Ar, Kr, Xe, CO, CH4, CH3OH, CO2 and N2 are used to probe the photochemical interactions of O2 on rutile TiO2(110). UV irradiation of chemisorbed O2 along with the physisorbed probe species leads to photon-stimulated desorption (PSD) of Ar, Kr, CO, CH4 and N2. Without co-adsorbed O2, the PSD yields of the probe species are very low or not observed. No PSD was observed for CO2, N2O, CH3OH and the PSD yield for Xe is very low compared to the other probe atoms or molecules. The angular distribution of the photo-desorbing Kr, which is broad and cosine, is quite different from the O2 PSD angular distribution, which is sharply peaked along the surface normal. The Kr PSD yields increase with increasing coverage of Kr and of chemisorbed O2. We propose a mechanism for the observed phenomena where the chemisorbed O2 serves as photoactive center, excited via electronic excitations (electrons and/or holes) created in the TiO2 substrate by UV photon irradiation. The photo-excited O2 may transfer its energy to neighboring co-adsorbed atom or molecule resulting in desorption of the latter. Simple momentum transfer considerations suggest that heavier adsorbates (like Xe) and adsorbates with higher binding energy (like CO2) should desorb less efficiently according to the proposed mechanism. Various forms of chemisorbed O2 appeared photoactive in such stimulated desorption of Kr atoms: molecular anions (O22-, O2-), adatoms (Oa), and others. The observed phenomenon provides a new tool for study of photocatalysis.

  2. Carbonate Ion Effects on Coccolith Carbon and Oxygen Isotopes

    NASA Astrophysics Data System (ADS)

    Ziveri, P.; Probert, I.; Stoll, H. M.

    2006-12-01

    The stable oxygen and carbon isotopic composition of biogenic calcite constitutes one of the primary tools used in paleoceanographic reconstructions. The δ18O of shells of ocean floor microfossils and corals reflects the composition of the paleo-seawater as they use the oxygen to build up their calcite and aragonite shells. The δ13C is used to reconstruct variations in the carbon isotopic composition of dissolved inorganic carbon in the ocean, which is controlled by biological productivity through the removal of isotopically light carbon in organic matter. To be effective and sensitive tools for understanding photic zone processes it is first necessary to understand the various biological fractionations associated with carbonate precipitation. To date, isotopic fractionation models are mainly based on foraminifera and corals but not on coccoliths, tiny plates produced by coccolithophore algae, which are often the most dominant carbonate contributors to pelagic sediments. As photosynthetic organisms, their chemistry can provide a sensitive tool for understanding photic zone processes. Coccoliths may be the most important carbonate phase for geochemical analysis in sediments where foraminifera are less common and/or core material is limited, such as in subpolar regions and for Early Cenozoic and Mesozoic sediments. Here we report experimental results on a common living coccolithophore species showing that the 13C/12C and 18O/16O ratios decrease with the increase of HCO^{3-} (CO32-). The selected species are among the heaviest calcifying extant coccolithophores and are major contributors to present coccolith carbonate export production. Because coccolithophores are photosynthetic organisms that calcify intracellularly in specialized vesicles, the challenge lies in ascertaining how kinetic and thermodynamic processes of isotopic fractionation are linked to cellular carbon "transport" and carbonate precipitation. This is a daunting challenge since studies have not

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

    SciTech Connect

    Horner, D.A.

    1984-08-01

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

  4. Simple preparation of aminothiourea-modified chitosan as corrosion inhibitor and heavy metal ion adsorbent.

    PubMed

    Li, Manlin; Xu, Juan; Li, Ronghua; Wang, Dongen; Li, Tianbao; Yuan, Maosen; Wang, Jinyi

    2014-03-01

    By a simple and convenient method of using formaldehyde as linkages, two new chitosan (CS) derivatives modified respectively with thiosemicarbazide (TSFCS) and thiocarbohydrazide (TCFCS) were synthesized. The new compounds were characterized and studied by Fourier transform infrared spectroscopy, elemental analysis, thermal gravity analysis and differential scanning calorimetry, and their surface morphologies were determined via scanning electron microscopy. These CS derivatives could form pH dependent gels. The behavior of 304 steel in 2% acetic acid containing different inhibitors or different concentrations of inhibitor had been studied by potentiodynamic polarization test. The preliminary results show that the new compound TCFCS can act as a mixed-type metal anticorrosion inhibitor in some extent; its inhibition efficiency is 92% when the concentration was 60 mg/L. The adsorption studies on a metal ion mixture aqueous solution show that two samples TSFCS and TCFCS can absorb As (V), Ni (II), Cu (II), Cd (II) and Pb (II) efficiently at pH 9 and 4.

  5. Oxygen Pickup Ions Measured by MAVEN Outside the Martian Bow Shock

    NASA Astrophysics Data System (ADS)

    Rahmati, A.; Cravens, T.; Larson, D. E.; Lillis, R. J.; Dunn, P.; Halekas, J. S.; Connerney, J. E. P.; Eparvier, F. G.; Thiemann, E.; Mitchell, D. L.; Jakosky, B. M.

    2015-12-01

    The MAVEN (Mars Atmosphere and Volatile EvolutioN) spacecraft entered orbit around Mars on September 21, 2014 and has since been detecting energetic oxygen pickup ions by its SEP (Solar Energetic Particles) and SWIA (Solar Wind Ion Analyzer) instruments. The oxygen pickup ions detected outside the Martian bowshock and in the upstream solar wind are associated with the extended hot oxygen exosphere of Mars, which is created mainly by the dissociative recombination of molecular oxygen ions with electrons in the ionosphere. We use analytic solutions to the equations of motion of pickup ions moving in the undisturbed upstream solar wind magnetic and motional electric fields and calculate the flux of oxygen pickup ions at the location of MAVEN. Our model calculates the ionization rate of oxygen atoms in the exosphere based on the hot oxygen densities predicted by Rahmati et al. (2014), and the sources of ionization include photo-ionization, charge exchange, and electron impact ionization. The photo-ionization frequency is calculated using the FISM (Flare Irradiance Spectral Model) solar flux model, based on MAVEN EUVM (Extreme Ultra-Violet Monitor) measurements. The frequency of charge exchange between a solar wind proton and an oxygen atom is calculated using MAVEN SWIA solar wind proton flux measurements, and the electron impact ionization frequency is calculated based on MAVEN SWEA (Solar Wind Electron Analyzer) solar wind electron flux measurements. The solar wind magnetic field used in the model is from the measurements taken by MAVEN MAG (magnetometer) in the upstream solar wind. The good agreement between our predicted pickup oxygen fluxes and the MAVEN SEP and SWIA measured ones confirms detection of oxygen pickup ions and these model-data comparisons can be used to constrain models of hot oxygen densities and photochemical escape flux.

  6. Preparation of Polypropylene Spin Tips Filled with Immobilized Titanium(IV) Ion Monolithic Adsorbent for Robust Phosphoproteome Analysis.

    PubMed

    Liu, Fangjie; Wan, Hao; Liu, Zhongshan; Wang, Hongwei; Mao, Jiawei; Ye, Mingliang; Zou, Hanfa

    2016-05-17

    In this study, we developed a Ti(IV) monolithic spin tip for phosphoproteome analysis of a minute amount of biological sample for the first time. The surface of polypropylene pipet tip was activated by the photoinitiator benzophenone under UV light radiation followed by polymerization of ethylene glycol methacrylate phosphate and bis-acrylamide in the tip to form a porous monolith with reactive phosphate groups. The as-prepared tips grafted with monolithic adsorbent were then chelated with titanium(IV) ion for phosphopeptide enrichment. It was found that the tips enabled fast and efficient capture of phosphopeptides from microscale complex samples. The monolithic tip was demonstrated to have a detection limit as low as 5 fmol β-casein tryptic digest, along with an exceptionally high specificity to capture phosphopeptides from complex tryptic digest mixed with an unphosphorylated protein and a phosphorylated protein at a molar ratio up to 1000:1. When the tip was applied to enrich phosphopeptides from 5 μg of tryptic digest of complex HeLa cell proteins, 1185 high confidence of phosphorylated sites were successfully identified with the specificity as high as 92.5%. So far, this is the most sensitive phosphoproteomics analysis using a standard liquid chromatography-tandem mass spectrometry (LC-MS/MS) system for proteome-wide phosphorylation analysis in mammalian cells. PMID:27101427

  7. Oxygen foreshock of Mars and its implication on ion acceleration in the bow shock

    NASA Astrophysics Data System (ADS)

    Yamauchi, Masatoshi; Lundin, Rickard; Frahm, Rudy; Sauvaud, Jean-Andre; Holmstrom, Mats; Barabash, Stas

    2016-04-01

    Ion acceleration inside the bow shock is one of the poorly understood phenomena that has been observed for more than 30 years as the foreshock phenomena. While the Fermi-acceleration mechanism explains the diffuse component of foreshock ions, we still do not know the detailed mechanism that produces the discrete intense ions flowing along the local magnetic field direction (with and without gyration). One of the reasons for such difficulty is that majority of the bow shock study was performed for the Earth's case where Oxygen ions cannot be used to understand the acceleration mechanisms. The planetary oxygen ions that reach the Earth's bow shock have already been significantly accelerated, and are not adequate for such a study. In this sense the Martian bow shock is an ideal place to study the acceleration mechanisms leading to foreshock ions, although the nature of the bow shock is slightly different between the Earth and Mars (Yamauchi et al., 2011). On 21 September 2008, the Mars Express (MEX) Ion Mass Analyser (IMA) detected foreshock-like discrete distributions of oxygen ions at around 1 keV in the solar wind attached to the bow shock. This was the first time that a substantial amount of planetary oxygen was observed upstream of the bow shock. The oxygen energy increased from low energy (< 300 keV) inside the magnetosheath (or it should be called an extended bow shock) to nearly 2 keV at more than 2000 km from the bow shock. Foreshock-like protons are also observed but at a shifted location from the oxygen by about 1000 km, at a slightly higher energy, and flowing in a slightly different direction than the oxygen ions. Both protons and oxygen ions are flowing anti-sunward at different angles with respect to the solar wind direction. The observation is consistent with an electric potential barrier at the bow shock that simultaneously accelerates the planetary oxygen ions outward (to form the foreshock oxygen ions) and reflects a portion of the solar wind (to

  8. The influence of oxygen-17 enriched oxygen-donor ligands on the electronic spin relaxation behaviour of paramagnetic metal ions

    NASA Astrophysics Data System (ADS)

    Wells, Gregg B.; Yim, Moon B.; Makinen, Marvin W.

    Continuous wave microwave power saturation of high-spin paramagnetic metalloprotein complexes of Co2+ and Fe3+ showed that the value of the saturation parameter P1/2 is influenced by the coordination of oxygen-17 enriched water to the metal ion. No change was observed for H218O or 2H2O. Pulse saturation and recovery of paramagnetic high-spin Fe3+ heme proteins identified a fast relaxation component sensitive to isotopic oxygen-17 composition that was assigned to the process of spectral diffusion. It is shown that the change in relaxation time for spectral diffusion can alter the (apparent) spin-lattice relaxation to account for the observed changes in continuous wave microwave power saturation experiments. These changes are shown to correlate with alterations in the extent of covalency between the metal ion and oxygen-donor ligand. The experimental results provide a basis for use of continuous wave microwave saturation to identify the presence of oxygen-donor ligands within the inner coordination shell of high-spin Co2+ or Fe3+ in metalloprotein and small molecule complexes and to qualitatively assess the extent of covalency between the metal ion and the oxygen-donor ligand.

  9. Oxygen Pickup Ions Measured by MAVEN: A Link to the Extended Exosphere of Mars

    NASA Astrophysics Data System (ADS)

    Rahmati, A.; Cravens, T.; Larson, D. E.; Fox, J. L.; Bougher, S. W.; Lillis, R. J.; Ledvina, S. A.; Dunn, P.

    2014-12-01

    The exosphere of Mars is very extensive and the hot oxygen corona, produced photochemically in the ionosphere, extends tens of Martian radii from the planet. This exosphere is a source of oxygen ions, picked up by the solar wind electric and magnetic fields, and accelerated toward Mars. The pickup ion energies depend on solar wind conditions and during high speed solar winds (> 500 km/s) with large angles between the solar wind bulk flow velocity and the interplanetary magnetic field (> 50 degrees), oxygen pickup ions can reach energies high enough (> 60 keV) to be detected by SEP. The SEP (Solar Energetic Particle) instrument is an energetic particle detector on board the MAVEN (Mars Atmosphere and Volatile EvolutioN) spacecraft, scheduled to reach Mars in September 2014. In this study, the instrumental geometry and response function of SEP are included in a modeling analysis of the effect that different solar wind conditions and SEP look directions will have on O+ pickup ion energy spectra. We describe a method that provides constraints on neutral oxygen escape models by linking the SEP energy spectra to the photochemical source of hot oxygen. Additionally, we present model results for pick-up ion distributions, and their possible detection by the SEP, STATIC (SupraThermal And Thermal Ion Composition) and SWIA (Solar Wind Ion Analyzer) instruments on board MAVEN, during the close passage of Comet Siding Spring to Mars on October 19, 2014. Large ion flux enhancements near Mars originating from the comet's neutral coma are predicted.

  10. Ion implantation method for preparing polymers having oxygen erosion resistant surfaces

    DOEpatents

    Lee, E.H.; Mansur, L.K.; Heatherly, L. Jr.

    1995-04-18

    Hard surfaced polymers and the method for making them are generally described. Polymers are subjected to simultaneous multiple ion beam bombardment, that results in a hardening of the surface, improved wear resistance, and improved oxygen erosion resistance. 8 figs.

  11. Ion implantation method for preparing polymers having oxygen erosion resistant surfaces

    DOEpatents

    Lee, Eal H.; Mansur, Louis K.; Heatherly, Jr., Lee

    1995-01-01

    Hard surfaced polymers and the method for making them are generally described. Polymers are subjected to simultaneous multiple ion beam bombardment, that results in a hardening of the surface, improved wear resistance, and improved oxygen erosion resistance.

  12. Transverse acceleration of oxygen ions by electromagnetic ion cyclotron resonance with broad band left-hand polarized waves

    NASA Technical Reports Server (NTRS)

    Chang, T.; Crew, G. B.; Hershkowitz, N.; Jasperse, J. R.; Retterer, J. M.

    1986-01-01

    Central plasma sheet (CPS) ion conics are oxygen-dominated, with peak energies ranging from tens to hundreds of eV centered around pitch-angles between 115 and 130 degrees. Because of the lack of correlation between the CPS conics and the observed currents and/or electron beam-like structures, it is not likely that all of these conics are generated by interactions with electrostatic ion cyclotron waves or lower hybrid waves. Instead, it is suggested that the observed intense broad band electric field fluctuations in the frequency range between 0 and 100 Hz can be responsible for the transverse energization of the ions through cyclotron resonance heating with the left-hand polarized electromagnetic waves. This process is much more efficient for heating the oxygen ions than hydrogen ions, thus providing a plausible explanation of the oxygen dominance in CPS conics. Simple algebraic expressions are given from which estimates of conic energy and pitch angle can be easily calculated. This suggested mechanism can also provide some preheating of the oxygen ions in the boundary plasma sheet (BPS) where discrete aurorae form.

  13. Purification of equine chorionic gonadotropin (eCG) using magnetic ion exchange adsorbents in combination with high-gradient magnetic separation.

    PubMed

    Müller, Christine; Heidenreich, Elena; Franzreb, Matthias; Frankenfeld, Katrin

    2015-01-01

    Current purification of the glycoprotein equine chorionic gonadotropin (eCG) from horse serum includes consecutive precipitation steps beginning with metaphosphoric acid pH fractionation, two ethanol precipitation steps, and dialysis followed by a numerous of fixed-bed chromatography steps up to the specific activity required. A promising procedure for a more economic purification procedure represents a simplified precipitation process requiring only onethird of the solvent, followed by the usage of magnetic ion exchange adsorbents employed together with a newly designed 'rotor-stator' type High Gradient Magnetic Fishing (HGMF) system for large-scale application, currently up to 100 g of magnetic adsorbents. Initially, the separation process design was optimized for binding and elution conditions for the target protein in mL scale. Subsequently, the magnetic filter for particle separation was characterized. Based on these results, a purification process for eCG was designed consisting of (i) pretreatment of the horse serum; (ii) binding of the target protein to magnetic ion exchange adsorbents in a batch reactor; (iii) recovery of loaded functionalized adsorbents from the pretreated solution using HGMF; (iv) washing of loaded adsorbents to remove unbound proteins; (v) elution of the target protein. Finally, the complete HGMF process was automated and conducted with either multiple single-cycles or multicycle operation of four sequential cycles, using batches of pretreated serum of up to 20 L. eCG purification with yields of approximately 53% from single HGMF cycles and up to 80% from multicycle experiments were reached, with purification and concentration factors of around 2,500 and 6.7, respectively.

  14. Growth of nickel nanoparticles on NiO/Ni(0 0 1): Evidence of adsorbed oxygen on metal particles by metastable induced electron spectroscopy (MIES)

    NASA Astrophysics Data System (ADS)

    Berlich, Andrea; Liu, Yan-Chun; Morgner, Harald

    2008-12-01

    We present results - obtained with X-ray as well as ultraviolet photoelectron spectroscopy (XPS and UPS) and metastable induced electron spectroscopy (MIES) - for the deposition of nickel on a NiO film of about 10 monolayers. It was found that up to a coverage of 0.5 monolayers single atoms or non-metallic clusters with up to 7 nickel atoms are formed. A MIES reference spectrum for this situation has been reconstructed from the experimental spectral series and the surface density of states has been obtained by deconvolution of this spectrum. Above 0.5 monolayer nominal nickel coverage a metallic nickel overlayer is formed as indicated by UPS. However, only MIES with its perfect surface sensitivity provides direct experimental evidence that on top of the metallic nickel a small amount of oxygen is adsorbed which originates from the underlying oxide.

  15. High-LET ion radiolysis of water: oxygen production in tracks.

    PubMed

    Meesungnoen, Jintana; Jay-Gerin, Jean-Paul

    2009-03-01

    It is known that molecular oxygen is a product of the radiolysis of water with high-linear energy transfer (LET) radiation, a result that is of particular significance in radiobiology and of practical relevance in radiotherapy. In fact, it has been suggested that the radiolytic formation of an oxygenated microenvironment around the tracks of high-LET heavy ions is an important factor in their enhanced biological efficiency in the sense that this may be due to an "oxygen effect" by O(2) produced by these ions in situ. Using Monte Carlo track simulations of pure, deaerated water radiolysis by 4.8 MeV (4)He(2+) (LET approximately 94 keV/microm) and 24 MeV (12)C(6+) (LET approximately 490 keV/microm) ions, including the mechanism of multiple ionization of water, we have calculated the yields and concentrations of O(2) in the tracks of these irradiating ions as a function of time between approximately 10(-12) and 10(-5) s at 25 and 37 degrees C. The track oxygen concentrations obtained compare very well with O(2) concentrations estimated from the "effective" amounts of oxygen that are needed to produce the observed reduction in oxygen enhancement ratio (OER) with LET (assuming this decrease is attributable to the sole radiolytic formation of O(2) in the tracks). For example, for 24 MeV (12)C(6+) ions, the initial track concentration of O(2) is estimated to be more than three orders of magnitude higher than the oxygen levels present in normally oxygenated and hypoxic tumor regions as well as in normal human cells. Such results, which largely plead in favor of the "oxygen in the heavy-ion track" hypothesis, could explain at least in part the greater efficiency of high-LET radiation for cell inactivation (at equal radiation dose). PMID:19267566

  16. Counterstreaming hydrogen and oxygen ions observed in the magnetosphere on ISEE-1

    NASA Technical Reports Server (NTRS)

    Horita, R. E.; Ungstrup, E.; Sharp, R. D.; Anderson, R. R.; Fitzenreiter, R. J.

    1985-01-01

    Counterstreaming ions or ions travelling simultaneously both parallel and antiparallel to the magnetic field direction have been briefly noted in the literature but have not been studied previously in depth. Over 60 counterstreaming ion (CSI) events observed on the ISEE-1 satellite have been studied. They were found to occur at altitudes of about 2 to 8 earth radii on L shells of about 5 to 12 in the evening-to-morning sector from about 1700-0900 LT. Often both oxygen and hydrogen ions at a number of energy levels are counterstreaming but some events show only either oxygen or hydrogen ions involved. One particularly interesting event shows only counterstreaming oxygen ions with 417 eV energy; oxygen ions of lower energy (215 eV) and above (630-17,000 eV) and all the hydrogen ions between 215-17,000 eV energy have lower fluxes and/or nearly isotropic pitch angle distributions. This event correlates well with wave activity in the 17-100 Hz band and is also accompanied by 200 eV downgoing and 400 eV upgoing electrons. Details of this event and the other counterstreaming events are presented.

  17. Simulation of the low earth orbital atomic oxygen interaction with materials by means of an oxygen ion beam

    NASA Technical Reports Server (NTRS)

    Banks, Bruce A.; Rutledge, Sharon K.; Paulsen, Phillip E.; Steuber, Thomas J.

    1989-01-01

    Atomic oxygen is the predominant species in low-Earth orbit between the altitudes of 180 and 650 km. These highly reactive atoms are a result of photodissociation of diatomic oxygen molecules from solar photons having a wavelength less than or equal to 2430A. Spacecraft in low-Earth orbit collide with atomic oxygen in the 3P ground state at impact energies of approximately 4.2 to 4.5 eV. As a consequence, organic materials previously used for high altitude geosynchronous spacecraft are severely oxidized in the low-Earth orbital environment. The evaluation of materials durability to atomic oxygen requires ground simulation of this environment to cost effectively screen materials for durability. Directed broad beam oxygen sources are necessary to evaluate potential spacecraft materials performance before and after exposure to the simulated low-Earth orbital environment. This paper presents a description of a low energy, broad oxygen ion beam source used to simulate the low-Earth orbital atomic oxygen environment. The results of materials interaction with this beam and comparison with actual in-space tests of the same meterials will be discussed. Resulting surface morphologies appear to closely replicate those observed in space tests.

  18. Energization of Oxygen Ions at Mars: Comparison of a Global Hybrid Model to In Situ Observations

    NASA Astrophysics Data System (ADS)

    Jarvinen, R.; Brain, D. A.; Fedorov, A.; Holmstrom, M.; Modolo, R.

    2015-12-01

    We study the energization of planetary oxygen ions escaping from the atmosphere of Mars in a global hybrid model for the Mars-solar wind interaction. In the hybrid approach ions are modelled as particles moving under the Lorentz force and electrons are a charge-neutralizing fluid. Thus, electric and magnetic field are self-consistently coupled with ion dynamics. We identify ion energization regions in the induced magnetosphere of Mars in the model. Further, we study electric and magnetic fields associated with the ion acceleration processes. Finally, we compare our simulation results to in situ particle and magnetic field observations on the MAVEN and Mars Express missions.

  19. Carbon, nitrogen, and oxygen ion implantation of stainless steel

    SciTech Connect

    Rej, D.J.; Gavrilov, N.V.; Emlin, D.

    1995-12-31

    Ion implantation experiments of C, N, and O into stainless steel have been performed, with beam-line and plasma source ion implantation methods. Acceleration voltages were varied between 27 and 50 kV, with pulsed ion current densities between 1 and 10 mA/cm{sup 2}. Implanted doses ranged from 0.5 to 3 {times} 10{sup 18}cm{sup -2}, while workpiece temperatures were maintained between 25 and 800 C. Implant concentration profiles, microstructure, and surface mechanical properties of the implanted materials are reported.

  20. Argon–oxygen dc magnetron discharge plasma probed with ion acoustic waves

    SciTech Connect

    Saikia, Partha Saikia, Bipul Kumar; Goswami, Kalyan Sindhu; Phukan, Arindam

    2014-05-15

    The precise determination of the relative concentration of negative ions is very important for the optimization of magnetron sputtering processes, especially for those undertaken in a multicomponent background produced by adding electronegative gases, such as oxygen, to the discharge. The temporal behavior of an ion acoustic wave excited from a stainless steel grid inside the plasma chamber is used to determine the relative negative ion concentration in the magnetron discharge plasma. The phase velocity of the ion acoustic wave in the presence of negative ions is found to be faster than in a pure argon plasma, and the phase velocity increases with the oxygen partial pressure. Optical emission spectroscopy further confirms the increase in the oxygen negative ion density, along with a decrease in the argon positive ion density under the same discharge conditions. The relative negative ion concentration values measured by ion acoustic waves are compared with those measured by a single Langmuir probe, and a similarity in the results obtained by both techniques is observed.

  1. Fast, selective adsorption of Cu{sup 2+} from aqueous mixed metal ions solution using 1,4,7-triazacyclononane modified SBA-15 silica adsorbent (SBA-TACN)

    SciTech Connect

    Tapaswi, Pradip Kumar; Moorthy, Madhappan Santha; Park, Sung Soo; Ha, Chang-Sik

    2014-03-15

    A new SBA-15 supported 1,4,7-triazacyclononane modified mesoporous silica adsorbent (SBA-TACN) has been synthesized using post grafting route and has thoroughly been characterized by small angle X-ray scattering (SAXS), N{sub 2} adsorption–desorption measurements, Fourier-transform infrared (FT-IR), solid-state {sup 29}Si MAS and {sup 13}C CP MAS NMR spectroscopy, transmission electron (TEM) and scanning electron microscopy (SEM), elemental analysis (EA) and thermogravimetric analysis (TGA). The synthesized material shows excellent copper (II) ion adsorption selectivity at pH 5 in mixed metal ion solution containing Cu{sup 2+}, Cr{sup 3+}, Ni{sup 2+}, Co{sup 2+} and Li{sup +}. The copper ion adsorption capacity of the SBA-TACN can reach a maximum value of 0.67 mmol/g. Possible adsorption mechanism of metal ions on SBA-TACN has been discussed. The adsorbent can be readily regenerated by HNO{sub 3}–NH{sub 3} treatment. -- Graphical abstract: A new SBA-15 supported 1,4,7-triazacyclononane (TACN) modified mesoporous silica (SBA-TACN) adsorbent has been developed which shows excellent selectivity in Cu{sup 2+} adsorption from aqueous mixed metal ion solutions at pH 5. The copper ion adsorption capacity of the SBA-TACN can reach a maximum value of 0.67 mmol/g. The adsobent is stable enough to be used atleast for three cycles. Highlights: • Synthesis of a new TACN modified mesoporous silica SBA-15 type adsorbent. • The density of 1,4,7-triazacyclononane on SBA-15 is 1.22 mmol/g. • First report on the selective Cu{sup 2+} adsorption by TACN modified mesoporous silica. • Cu{sup 2+} adsorption capacity of the SBA-TACN can reach a maximum value of 0.67 mmol/g. • Potential candidate for selective removal of Cu{sup 2+} from contaminated water samples.

  2. Effect of nature of oxygen interactions on friction of titanium, aluminum, and molybdenum

    NASA Technical Reports Server (NTRS)

    Buckley, D. H.

    1976-01-01

    Friction studies were conducted with a gold pin contacting titanium, aluminum, and molybdenum surfaces after exposure to oxygen with various methods. Oxygen was adsorbed on the surface, it reacted with the surface, and the surface was ion bombarded with oxygen. The presence of oxygen was monitored with Auger spectroscopy. Titanium friction varied with the mode of the metal-oxygen interaction. It was highest with the adsorbed oxygen and least with ion bombardment using oxygen. Aluminum exhibited lower friction values for the reacted and the ion bombarded surfaces than for the surface having the adsorbed layer. With molybdenum the friction coefficients were generally the same despite the nature of the surface treatment with oxygen.

  3. The behaviour of negative oxygen ions in the afterglow of a reactive HiPIMS discharge

    NASA Astrophysics Data System (ADS)

    Bowes, M.; Bradley, J. W.

    2014-07-01

    Using a single Langmuir probe, the temporal evolution of the oxygen negative ion, n-, and electron, ne, densities in the afterglow of a reactive HiPIMS discharge operating in argon-oxygen gas mixtures have been determined. The magnetron was equipped with a titanium target and operated in ‘poisoned’ mode at a frequency of 100 Hz with a pulse width of 100 µs for a range of oxygen partial pressures, {p_{O_{2}}}/{p_{total}} = 0.0{{-}}0.5 . In the initial afterglow, the density of the principle negative ion in the discharge (O-) was of the order of 1016 m-3 for all conditions. The O- concentration was found to decay slowly with characteristic decay times between 585 µs and 1.2 ms over the oxygen partial pressure range. Electron densities were observed to fall more rapidly, resulting in long-lived highly electronegative afterglow plasmas where the ratio, α = n-/ne, was found to reach values up to 672 (±100) for the highest O2 partial pressure. By comparing results to a simple plasma-chemical model, we speculate that with increased {p_{O_{2}}}/{p_{total}} ratio, more O- ions are formed in the afterglow via dissociative electron attachment to highly excited metastable oxygen molecules, with the latter being formed during the active phase of the discharge. After approximately 2.5 ms into the off-time, the afterglow degenerates into an ion-ion plasma and negative ions are free to impinge upon the chamber walls and grounded substrates with flux densities of the order of 1018 m-2 s-1, which is around 10% of the positive ion flux measured during the on-time. This illustrates the potential importance of the long afterglow in reactive HiPIMS, which can act as a steady source of low energy O- ions to a growing thin film at the substrate during periods of reduced positive ion bombardment.

  4. Effect of adsorbed metals ions on the transport of Zn- and Ni-EDTA complexes in a sand and gravel aquifer

    USGS Publications Warehouse

    Kent, D.B.; Davis, J.A.; Anderson, L.C.D.; Rea, B.A.; Coston, J.A.

    2002-01-01

    Adsorption, complexation, and dissolution reactions strongly influenced the transport of metal ions complexed with ethylenediaminetetraacetic acid (EDTA) in a predominantly quartz-sand aquifer during two tracer tests conducted under mildly reducing conditions at pH 5.8 to 6.1. In tracer test M89, EDTA complexes of zinc (Zn) and nickel (Ni), along with excess free EDTA, were injected such that the lower portion of the tracer cloud traveled through a region with adsorbed manganese (Mn) and the upper portion of the tracer cloud traveled through a region with adsorbed Zn. In tracer test S89, Ni- and Zn-EDTA complexes, along with excess EDTA complexed with calcium (Ca), were injected into a region with adsorbed Mn. The only discernable chemical reaction between Ni-EDTA and the sediments was a small degree of reversible adsorption leading to minor retardation. In the absence of adsorbed Zn, the injected Zn was displaced from EDTA complexes by iron(III) [Fe(III)] dissolved from the sediments. Displacement of Zn by Fe(III) on EDTA became increasingly thermodynamically favorable with decreasing total EDTA concentration. The reaction was slow compared to the time-scale of transport. Free EDTA rapidly dissolved aluminum (Al) from the sediments, which was subsequently displaced slowly by Fe. In the portion of tracer cloud M89 that traveled through the region contaminated with adsorbed Zn, little displacement of Zn complexed with EDTA was observed, and Al was rapidly displaced from EDTA by Zn desorbed from the sediments, in agreement with equilibrium calculations. In tracer test S89, desorption of Mn dominated over the more thermodynamically favorable dissolution of Al oxyhydroxides. Comparison with results from M89 suggests that dissolution of Al oxyhydroxides in coatings on these sediment grains by Ca-EDTA was rate-limited whereas that by free EDTA reached equilibrium on the time-scale of transport. Rates of desorption are much faster than rates of dissolution of Fe

  5. Charge exchange of metastable 2D oxygen ions with molecular oxygen - A new source of thermospheric O2/+/ ions

    NASA Technical Reports Server (NTRS)

    Torr, D. G.; Torr, M. R.; Rusch, D. W.; Nier, A. O.; Kayser, D.; Hanson, W. B.; Hoffman, J. H.; Donahue, K.

    1979-01-01

    Reactions involving metastable ions are difficult to study in the laboratory. Much new information on these reactions has been derived from satellite measurements of aeronomic parameters. In this paper, Atmosphere Explorer D data are used to study charge exchange of metastable O(+)(2D) ions with O2. Using direct measurements of the O2 at 200 km to compute O2 densities at 300 km and supporting ionic concentrations and temperature observations, we find the rate coefficient for this reaction to be 1 + or - 0.6 times 10 to the minus 9th cu cm/sec. The process constitutes a significant source of O2(+) ions in the F2 layer at times when the N2 and O2 densities are enhanced. This finding leads to the conclusion that charge exchange with O2 must be a major sink for O(+)(2D) and an important source of O2(+) ions in the E region, because of the increase in the O2 concentration/N2 concentration ratio with decreasing altitude. The results imply that 80% of all O(+) ions formed in the E region are converted to O2(+) and that only about 20% of the metastable O(+) ions are converted into N2(+) through charge exchange with N2.

  6. Oxygen Ion Heat Rate within Alfvenic Turbulence in the Cusp

    NASA Technical Reports Server (NTRS)

    Coffey, Victoria N.; Singh, Nagendra; Chandler, Michael O.

    2009-01-01

    The role that the cleft/cusp has in ionosphere-magnetosphere coupling makes it a dynamic and important region. It is directly exposed to the solar wind, making it possible for the entry of electromagnetic energy and precipitating electrons and ions from dayside reconnection and other dayside events. It is also a significant source of ionospheric plasma, contributing largely to the mass loading of the magnetosphere with large fluxes of outflowing ions. Crossing the cusp/cleft near 5100 km, the Polar instruments observe the common correlation of downward Poynting flux, ion energization, soft electron precipitation, broadband extremely low-frequency (BB-ELF) emissions, and density depletions. The dominant power in the BB-ELF emissions is now identified to be from spatially broad, low frequency Alfv nic structures. For a cusp crossing, we determine using the Electric Field Investigation (EFI), that the electric and magnetic field fluctuations are Alfv nic and the electric field gradients satisfy the inequality for stochastic acceleration. With all the Polar 1996 horizontal crossings of the cusp, we determine the O+ heating rate using the Thermal Ion Dynamics Experiment (TIDE) and Plasma Wave Investigation (PWI). We then compare this heating rate to other heating rates assuming the electric field gradient criteria exceeds the limit for stochastic acceleration for the remaining crossings. The comparison suggests that a stochastic acceleration mechanism is operational and the heating is controlled by the transverse spatial scale of the Alfvenic waves.

  7. Heavy Ion Formation in Titan's Ionosphere: Magnetospheric Introduction of Free Oxygen and Source of Titan's Aerosols?

    NASA Technical Reports Server (NTRS)

    Sittler, E. C., Jr.; Hartle, R. E.; Cooper, J. F.; Johnson, R. E.; Coates, A.; dePater, imke; Strom, Daphne; Simoes, F.; Steele, A.; Robb, F.

    2007-01-01

    With the recent discovery of heavy ions, positive and negative, by the Cassini Plasma Spectrometer (CAPS) instrument in Titan's ionosphere, it reveals new possibilities for aerosol formation at Titan and the introduction of free oxygen to the aerosol chemistry from Saturn's magnetosphere with Enceladus as the primary oxygen source. One can estimate whether the heavy ions in the ionosphere are of sufficient number to account for all the aerosols, under what conditions are favorable for heavy ion formation and how they are introduced as seed particles deeper in Titan's atmosphere where the aerosols form and eventually find themselves on Titan's surface where unknown chemical processes can take place. Finally, what are the possibilities with regard to their chemistry on the surface with some free oxygen present in their seed particles?

  8. Distribution of hydrogen and oxygen ion species in the plasmasheet

    NASA Astrophysics Data System (ADS)

    Wang, Jing; Cao, Jinbin; Liu, Wenlong

    2016-07-01

    In this paper, using data obtained by Cluster 4 satellite from 2001 to 2012, we statistically investigate the spatial distributions of H+ and O+ in the magnetotail plasmasheet and their relation with geomagnetic indices. Our work outlines the existence of two regions with enhanced O+ concentration in the tail plasmasheet, one is located in the mid-tail plasmasheet at R > 17 RE, and the other is located near the inner boundary of plasmasheet at R < 10 RE. The existence of the depletion region of O+ between 10 RE < R < 17 RE indicates that the O+ ions in the mid-tail plasmasheet, which come from polar cap, are not likely to be able to make important contribution to the formation of ring current. Both the distributions of density and temperature of O+ ions have a dawn-dusk asymmetry. The number density of O+ during geomagnetic active time (Dst < -20 nT/AE > 200 nT/Kp ⩾ 3) is much larger than that during non-storm time (Dst > -20 nT/AE < 200 nT/Kp < 3). This dawn-dusk asymmetry and the number density of O+ varying with geomagnetic activity apply for both regions (R < 10 RE and R > 17 RE) of O+. Therefore both substorm and enhanced convection provide a large number of O+ ions to the plasmasheet, which makes favorable condition for the growth of the ring current.

  9. Secondary ion mass spectroscopy determination of oxygen diffusion coefficient in heavily Sb doped Si

    NASA Astrophysics Data System (ADS)

    Pagani, M.

    1990-10-01

    The diffusion coefficient of oxygen in heavily antimony doped Czochralski Si was measured in the temperature range 950-1100 °C by using secondary ion mass spectroscopy (SIMS). The diffusion coefficient, obtained from SIMS oxygen concentration profiles in samples submitted to out diffusion, shows no dependence on antimony concentration. The combined data give an activation energy of 2.68 eV, which is in good agreement with published results.

  10. Hydrogen removal from e-beam deposited alumina thin films by oxygen ion beam

    SciTech Connect

    Das, Arijeet Mukharjee, C. Rajiv, K. Bose, Aniruddha Singh, S. D. Rai, S. K.; Ganguli, Tapas; Joshi, S. C.; Deb, S. K.; Phase, D. M.

    2014-04-24

    Hydrogen interstitials and oxygen vacancies defects create energy levels in the band gap of alumina. This limits the application of alumina as a high-k dielectric. A low thermal budget method for removal of hydrogen from alumina is discussed. It is shown that bombardment of alumina films with low energy oxygen ion beam during electron beam evaporation deposition decreases the hydrogen concentration in the film significantly.

  11. Fabrication of a novel hydrophobic/ion-exchange mixed-mode adsorbent for the dispersive solid-phase extraction of chlorophenols from environmental water samples.

    PubMed

    Gao, Li; Wei, Yinmao

    2016-08-01

    A novel mixed-mode adsorbent was prepared by functionalizing silica with tris(2-aminoethyl)amine and 3-phenoxybenzaldehyde as the main mixed-mode scaffold due to the presence of the plentiful amino groups and benzene rings in their molecules. The adsorption mechanism was probed with acidic, natural and basic compounds, and the mixed hydrophobic and ion-exchange interactions were found to be responsible for the adsorption of analytes. The suitability of dispersive solid-phase extraction was demonstrated in the determination of chlorophenols in environmental water. Several parameters, including sample pH, desorption solvent, ionic strength, adsorbent dose, and extraction time were optimized. Under the optimal extraction conditions, the proposed dispersive solid-phase extraction coupled with high-performance liquid chromatography showed good linearity range and acceptable limits of detection (0.22∽0.54 ng/mL) for five chlorophenols. Notably, the higher extraction recoveries (88.7∽109.7%) for five chlorophenols were obtained with smaller adsorbent dose (10 mg) and shorter extraction time (15 min) compared with the reported methods. The proposed method might be potentially applied in the determination of trace chlorophenols in real water samples.

  12. Experiment and modeling of laser photodetachment of negative ions in helium oxygen barrier discharges

    NASA Astrophysics Data System (ADS)

    Tschiersch, Robert; Nemschokmichal, Sebastian; Meichsner, Jürgen

    2015-09-01

    Helium oxygen discharges operating at atmospheric pressure are of great interest for applications, such as surface treatment of biological samples. Helium as the buffer gas keeps the driving power low, and oxygen serves as the source of radicals. The large electronegativity of oxygen results in the formation of negative ions which in turn have a remarkable influence on the discharge development. To point out this role of negative ions, the change of the discharge behavior after the laser photodetachment of negative ions is measured in a helium oxygen barrier discharge. These measurements reveal a lower breakdown voltage when firing the laser during the pre-phase of the discharge. The reason is the additional pre-ionization by the detached electrons which was proved by an 1D numeric fluid modeling. The next step is the determination of absolute number densities of negative ions by a comparison of the experimental parameter variations with those from the modeling. Furthermore, the actual role of negative ions on the discharge behavior will be emphasized by the modeling.

  13. ATOMIC AND MOLECULAR PHYSICS: Guided transmission of oxygen ions through Al2O3 nanocapillaries

    NASA Astrophysics Data System (ADS)

    Chen, Yi-Feng; Chen, Xi-Meng; Lou, Feng-Jun; Xu, Jin-Zhang; Shao, Jian-Xiong; Sun, Guang-Zhi; Wang, Jun; Xi, Fa-Yuan; Yin, Young-Zhi; Wang, Xing-An; Xu, Jun-Kui; Cui, Ying; Ding, Bao-Wei

    2009-07-01

    The transmissions of oxygen ions through Al2O3 nanocapillaries each 50 nm in diameter and 10 μm in length at a series of different tilt angles are measured, where the ions with energies ranging from 10 to 60 keV and charge states from 1 up to 6 are involved. The angular distribution and the transmission yields of transported ions are investigated. Our results indicate both the existence of a guiding effect when ions pass through the capillary and a significant dependence of the ion transmission on the energy and the charge state of the ions. The guiding effects are observed to be enhanced at lower projectile energies and higher charge states. Meanwhile, the results also exhibit that the transmission yields increase as the tilt angle decreases at a given energy and charge state.

  14. Correlation between the sorption of dissolved oxygen onto chitosan and its antimicrobial activity against Esherichia coli.

    PubMed

    Gylienė, Ona; Servienė, Elena; Vepštaitė, Iglė; Binkienė, Rima; Baranauskas, Mykolas; Lukša, Juliana

    2015-10-20

    The ability of chitosan to adsorb dissolved oxygen from solution depends on its physical shape and is related to the surface area. Depending on conditions chitosan is capable of adsorbing or releasing oxygen. Chitosan, modificated by the substances possessing antimicrobial activity, such as succinic acid, Pd(II) ions, metallic Pd or Ag, distinctly increases the ability to adsorb the dissolved oxygen. The additional treatment of chitosan with air oxygen or electrochemically produced oxygen also increases the uptake of dissolved oxygen by chitosan. A strong correlation between the amount of oxygen adsorbed onto chitosan and its antimicrobial activity against Esherichia coli has been observed. This finding suggests that one of the sources of antimicrobial activity of chitosan is the ability to sorb dissolved oxygen, along with other well-known factors such as physical state and chemical composition.

  15. Correlation between oxygen vacancies and sites of Mn ions in YMnO{sub 3}

    SciTech Connect

    Cheng, Shaobo; Deng, S. Q.; Zhu, Jing; Zhao, Y. G.; Sun, X. F.

    2015-02-09

    In multiferroic hexagonal manganites (RMnO{sub 3}, R = Y, Sc, Ho-Lu), positions of Mn ions can affect both their in-plane and inter-plane exchange interactions, thus they are of utmost importance for the magneto-elastic coupling of rare-earth compounds. However, the reported in-plane positions of Mn ions by different groups are controversial and there is a lack of convenient method to identify the shift of Mn ions from the center of MnO{sub 5} bipyramids. Here, we demonstrate that the transmission electron microscopy is an efficient technique to characterize the positions of Mn ions and the shift of Mn ions can be directly recognized from the selected area electron diffraction (SAED) patterns. Through systematic studies on the SAED patterns acquired from regions with stoichiometric and non-stoichiometric ratio, we conclude that the intensities of (11{sup ¯}0) and (22{sup ¯}0) diffraction spots are very sensitive to the in-plane positions of Mn ions. We ascribe the off-centered shift of Mn ions to the in-plane oxygen vacancies and this is verified by combined electron microscopy and electron diffraction pattern calculations. Our results indicate that SAED can be used to judge both local positions of Mn ions and local oxygen deficiency in RMnO{sub 3} systems.

  16. Oxygen ion implantation induced microstructural changes and electrical conductivity in Bakelite RPC detector material

    NASA Astrophysics Data System (ADS)

    Kumar, K. V. Aneesh; Ranganathaiah, C.; Kumarswamy, G. N.; Ravikumar, H. B.

    2016-05-01

    In order to explore the structural modification induced electrical conductivity, samples of Bakelite Resistive Plate Chamber (RPC) detector materials were exposed to 100 keV Oxygen ion in the fluences of 1012, 1013, 1014 and 1015 ions/cm2. Ion implantation induced microstructural changes have been studied using Positron Annihilation Lifetime Spectroscopy (PALS) and X-Ray Diffraction (XRD) techniques. Positron lifetime parameters viz., o-Ps lifetime and its intensity shows the deposition of high energy interior track and chain scission leads to the formation of radicals, secondary ions and electrons at lower ion implantation fluences (1012 to1014 ions/cm2) followed by cross-linking at 1015 ions/cm2 fluence due to the radical reactions. The reduction in electrical conductivity of Bakelite detector material is correlated to the conducting pathways and cross-links in the polymer matrix. The appropriate implantation energy and fluence of Oxygen ion on polymer based Bakelite RPC detector material may reduce the leakage current, improves the efficiency, time resolution and thereby rectify the aging crisis of the RPC detectors.

  17. Theoretical analysis of the role of interfaces in transport through oxygen ion and electron conducting membranes

    NASA Astrophysics Data System (ADS)

    Virkar, Anil V.

    This manuscript examines transport through oxygen ion and electronic conducting membranes including electrode/membrane interfaces by explicitly incorporating both ionic and electronic transport through the membranes and across interfaces. Spatial variation of electrochemical potential of oxygen ions, μ, electrochemical potential of electrons, μ (or reduced negative electrochemical potential of electrons, φ=-μ/e, where e is the electronic charge), and chemical potential of molecular oxygen, μ, through membrane and across interfaces are examined as functions of transport properties of membranes and interfacial regions. The analysis shows that description of transport across electrode/membrane interfaces requires two transport parameters—one for ions, and the other for electrons. The transport equations are applied to fuel cells, pressure-driven oxygen separation through mixed ionic-electronic conducting (MIEC) membranes, and voltage-driven oxygen separation through predominantly oxygen ion conducting membranes. In fuel cells and MIEC oxygen separation membranes, the μ varies monotonically between the two end values corresponding to those at the two electrodes. Thus, in fuel cells and MIEC oxygen separation membranes, the stability of the membrane is assured as long as the oxygen partial pressure, p, on the fuel side or the permeate side is above the decomposition oxygen partial pressure of the membrane. By contrast, in voltage-driven oxygen separation membranes, μ in the membrane can lie outside of the end values. Thus, in the case of oxygen separation under an applied voltage, the transport properties of the material and the interfaces determine membrane stability. Implications of the analysis concerning the applicability of the so-called the three-electrode system under an applied voltage to investigate electrode polarization are presented. It is shown that the use of the three-electrode system for the estimation of electrode kinetics can lead to

  18. Ratiometric optical fiber sensor for dual sensing of copper ion and dissolved oxygen.

    PubMed

    Chu, Cheng-Shane; Chuang, Chih-Yung

    2015-12-20

    This paper develops a new ratiometric optical dual sensor for Cu2+ ions and dissolved oxygen (DO) incorporating a sol-gel matrix doped with palladium tetrakis pentafluorophenyl porphine as the oxygen-sensitive material, CdSe quantum dots as the Cu2+ ion-sensing material, and 7-amino-4-trifluoromethyl coumarin as the Cu2+ /DO practically independent fluorescent dye. The feasibility of coating an optical fiber with the sensing film to fabricate a ratiometric optical fiber dual sensor is investigated. Using an LED with a central wavelength of 405 nm as an excitation source, it is shown that the emission wavelengths of the Cu2+ ion-sensitive, DO-sensitive dye and the reference dye have no spectral overlap and therefore permit Cu2+ ion and DO concentration to be measured using a ratiometric-based method. The ratiometric optical fiber dual sensor has been tested with regard to monitoring different Cu2+ ion (0-10 μM) and DO concentrations (0-38 mg/L). The results show that the luminescence properties of the Cu2+ ion sensor are independent of the presence of the oxygen sensor and have a uniquely good linear response in the 0-10 μM range. The proposed ratiometric sensing approach presented in this study has the advantage of suppressing spurious fluctuations in the intensity of the excitation source. PMID:26837033

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

    PubMed

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

    2012-03-01

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

  20. ON THE FORMATION OF OZONE IN SOLAR SYSTEM OXYGEN ICES EXPOSED TO HEAVY IONS

    SciTech Connect

    Ennis, Courtney; Kaiser, Ralf I.

    2012-02-01

    Mimicking the bombardment of icy surfaces with heavy ions from solar system radiation fields, solid-phase molecular oxygen ({sup 32}O{sub 2}) and its isotope labeled analogue ({sup 36}O{sub 2}) were irradiated with monoenergetic carbon (C{sup +}), nitrogen (N{sup +}), and oxygen (O{sup +}) ions in laboratory experiments simulating the interaction of ions from the solar wind and those abundant in planetary magnetospheres. Online Fourier-transform infrared spectroscopy of the irradiated oxygen ices (12 K) showed that the yields of molecular ozone monomer (O{sub 3} {approx} 2 Multiplication-Sign 10{sup -3} molecules eV{sup -1} in {sup 32}O{sub 2}) were independent of the mass of the implanted C{sup +}, N{sup +}, and O{sup +} ions ({Phi}{sub max} = 4.0 Multiplication-Sign 10{sup 14} ions cm{sup -2}). The production of oxygen atoms in the solid was observed in the mid-IR stabilized via the [O{sub 3}...O] van der Waals complex. We expand on this inference by comparing the ozone yields induced by light particles (e{sup -}, H{sup +}, and He{sup +}) to the heavy ions (C{sup +}, N{sup +}, and O{sup +}) to provide compelling evidence that the abundance of radiolytic products in an oxygen-bearing solid is primarily dependent on electronic stopping regimes, which supersedes the contribution of nuclear stopping processes irrespective of the mass of the particle irradiation in the kinetic energy regime of solar wind and magnetospheric particles.

  1. Intraneuronal ion distribution during experimental oxygen/glucose deprivation. Routes of ion flux as targets of neuroprotective strategies.

    PubMed

    Lopachin, R M

    1999-01-01

    Ischemic neuronal injury appears to be mediated by disruption of subcellular ion distribution and, therefore, prevention of ion relocation might be neuroprotective. X-ray microanalysis was used to measure concentrations of Na, K, Ca and other elements in subcellular compartments (e.g., mitochondria) of CA1 neurons from oxygen/glucose-deprived (OGD) hippocampal slices. Results showed that OGD produced progressive loss of ion regulation in CA1 cells. Post-OGD reperfusion with normal media exacerbated the initial ion deregulation. To study neuroprotective mechanisms, we determined the ability of hypothermia (31 degrees C) or ion channel blockade to retard intraneuronal ion disruption induced by OGD/reperfusion. Whereas Ca2+ channel blockade (omega-conotoxin MVIIC, 3 microM) was ineffective, hypothermia and Na+ channel blockers (tetrodotoxin, TTX, 1 microM; lidocaine, 200 microM) reduced ion deregulation in subneuronal compartments. Blockade of glutamate receptors (AMPA, 10 microM; the non-NMDA receptor antagonist CNQX, 10 microM/100 microM glycine; the NMDA receptor antagonist CCP, 100 microM) during OGD/reperfusion provided nearly complete protection. These findings provide a foundation for identifying potential pharmacotherapeutic approaches and for discerning corresponding mechanisms of neuroprotection. PMID:10668426

  2. Surface modification of poly(propylene carbonate) by oxygen ion implantation

    NASA Astrophysics Data System (ADS)

    Zhang, Jizhong; Kang, Jiachen; Hu, Ping; Meng, Qingli

    2007-04-01

    Poly(propylene carbonate) (PPC) was implanted by oxygen ion with energy of 40 keV. The influence of experimental parameters was investigated by varying ion fluence from 1 × 10 12 to 1 × 10 15 ions/cm 2. XPS, SEM, surface roughness, wettability, hardness, and modulus were employed to investigate structure and properties of the as-implanted PPC samples. Eight chemical groups, i.e., carbon, C sbnd H, C sbnd O sbnd C, C sbnd O, O sbnd C sbnd O, C dbnd O, ?, and ? groups were observed on surfaces of the as-implanted samples. The species and relative intensities of the chemical groups changed with increasing ion fluence. SEM images displayed that irradiation damage was related strongly with ion fluence. Both surface-recovering and shrunken behavior were observed on surface of the PPC sample implanted with fluence of 1 × 10 15 ions/cm 2. As increasing ion fluence, the surface roughness of the as-implanted PPC samples increased firstly, reached the maximum value of 159 nm, and finally decreased down the minimum value. The water droplet contact angle of the as-implanted PPC samples changed gradually with fluence, and reached the minimum value of 70° with fluence of 1 × 10 15 ions/cm 2. The hardness and modulus of the as-implanted PPC samples increased with increasing ion fluence, and reached their corresponding maximum values with fluence of 1 × 10 15 ions/cm 2. The experimental results revealed that oxygen ion fluence closely affected surface chemical group, morphology, surface roughness, wettability, and mechanical properties of the as-implanted PPC samples.

  3. Spray-dried chitosan microspheres containing 8-hydroxyquinoline -5 sulphonic acid as a new adsorbent for Cd(II) and Zn(II) ions.

    PubMed

    Vitali, Luciano; Laranjeira, Mauro C M; Gonçalves, Norberto S; Fávere, Valfredo T

    2008-03-01

    In the present study, a new chelating adsorbent was prepared from chitosan microspheres cross-linked with glutaraldehyde by spray drying using 8-hydroxyquinoline -5 sulphonic acid as chelant agent (CTS-SX-CL). Microspheres of the new adsorbent were characterized by Raman spectroscopy, scanning electron microscopy (SEM) and energy-dispersive X-ray microanalysis (EDX). The effect of pH, contact time and concentration of metallic ions in solution were evaluated on the adsorption behavior of Cd(II) and Zn(II) by CTS-SX-CL. Adsorption was maximum for both Cd(II) and Zn(II) at pH 8.0. Adsorption kinetic curves were obtained and could be fit by the pseudo second-order adsorption model. An analysis of equilibrium adsorption data using the Langmuir isotherm model indicated that the maximum adsorption capacity of CTS-SX-CL was higher than that of CTS-CL for both ions investigated. The adsorption capacity increased 74% for Cd(II).

  4. Adsorbent phosphates

    NASA Technical Reports Server (NTRS)

    Watanabe, S.

    1983-01-01

    An adsorbent which uses as its primary ingredient phosphoric acid salts of zirconium or titanium is presented. Production methods are discussed and several examples are detailed. Measurements of separating characteristics of some gases using the salts are given.

  5. Charge states of energetic oxygen and sulfur ions in Jupiter's magnetosphere

    NASA Astrophysics Data System (ADS)

    Clark, G.; Mauk, B. H.; Paranicas, C.; Kollmann, P.; Smith, H. T.

    2016-03-01

    Pitch angle distributions of proton and energetic heavy ion fluxes near Europa's orbit have been measured by the Galileo Energetic Particles Detector (EPD). At similar energies, these distributions have important differences. If their source and transport processes are similar, as we hypothesize here, then it is difficult to reconcile their different pitch angle distributions. By looking at the same question, other researchers have proposed that the heavies are multiply charged, leading to differences in how the particles are lost. This could not be confirmed directly with EPD because that detector does not separate heavy ion measurements by charge state. However, indirect analyses of the data have extracted the charge state of a few sulfur events. We present here a complete list of ion injections observed with EPD over the whole mission. Energetic sulfur and oxygen charge states can be inferred through a dispersion analysis of dynamic injections that makes use of the charge-dependent nature of the gradient-curvature azimuthal drift. We find that sulfur is predominantly multiply charged, whereas oxygen is more evenly distributed between singly and doubly charged states. In addition to current theories on energetic heavy ion transport near the Europa region, we propose that charge gain for the oxygen ions (electron stripping) may play an important role in the character of energetic particles in that region.

  6. Uplift of Ionospheric Oxygen Ions During Extreme Magnetic Storms

    NASA Technical Reports Server (NTRS)

    Tsurutani, Bruce T.; Mannucci, Anthony J.; Verkhoglyadova, Olga P.; Huba, Joseph; Lakhina, Gurbax S.

    2013-01-01

    Research reported earlier in literature was conducted relating to estimation of the ionospheric electrical field, which may have occurred during the September 1859 Carrington geomagnetic storm event, with regard to modern-day consequences. In this research, the NRL SAMI2 ionospheric code has been modified and applied the estimated electric field to the dayside ionosphere. The modeling was done at 15-minute time increments to track the general ionospheric changes. Although it has been known that magnetospheric electric fields get down into the ionosphere, it has been only in the last ten years that scientists have discovered that intense magnetic storm electric fields do also. On the dayside, these dawn-to-dusk directed electric fields lift the plasma (electrons and ions) up to higher altitudes and latitudes. As plasma is removed from lower altitudes, solar UV creates new plasma, so the total plasma in the ionosphere is increased several-fold. Thus, this complex process creates super-dense plasmas at high altitudes (from 700 to 1,000 km and higher).

  7. Influence of argon and oxygen on charge-state-resolved ion energydistributions of filtered aluminum arcs

    SciTech Connect

    Rosen, Johanna; Anders, Andre; Mraz, Stanislav; Atiser, Adil; Schneider, Jochen M.

    2006-03-23

    The charge-state-resolved ion energy distributions (IEDs) in filtered aluminum vacuum arc plasmas were measured and analyzed at different oxygen and argon pressures in the range 0.5 8.0 mTorr. A significant reduction of the ion energy was detected as the pressure was increased, most pronounced in an argon environment and for the higher charge states. The corresponding average charge state decreased from 1.87 to 1.0 with increasing pressure. The IEDs of all metal ions in oxygen were fitted with shifted Maxwellian distributions. The results show that it is possible to obtain a plasma composition with a narrow charge-state distribution as well as a narrow IED. These data may enable tailoring thin-film properties through selecting growth conditions that are characterized by predefined charge state and energy distributions.

  8. Temperature dependences of the photoluminescence intensities of centers in silicon implanted with erbium and oxygen ions

    SciTech Connect

    Sobolev, N. A. Shtel’makh, K. F.; Kalyadin, A. E.; Shek, E. I.

    2015-12-15

    Low-temperature photoluminescence in n-Cz-Si after the implantation of erbium ions at an elevated temperature and subsequent implantation of oxygen ions at room temperature is studied. So-called X and W centers formed from self-interstitial silicon atoms, H and P centers containing oxygen atoms, and Er centers containing Er{sup 3+} ions are observed in the photoluminescence spectra. The energies of enhancing and quenching of photoluminescence for these centers are determined. These energies are determined for the first time for X and H centers. In the case of P and Er centers, the values of the energies practically coincide with previously published data. For W centers, the energies of the enhancing and quenching of photoluminescence depend on the conditions of the formation of these centers.

  9. Contribution of specifically adsorbed ions, water, and impurities to the surface enhanced Raman spectroscopy (SERS) of Ag electrodes

    NASA Astrophysics Data System (ADS)

    Pettinger, Bruno; Philpott, Michael R.; Gordon, Joseph G., II

    1981-01-01

    Surface enhanced Raman scattering (SERS) has been observed from silver electrodes for water (H2O and D2O) in the frequency region of the librational, bending, and stretching modes. Simultaneously, SERS has been observed for halide ions and some organic impurities. The appearance of SERS from water and halide ions under the circumstances of the experiment is attributed to the formation of surface complexes involving silver adatoms, halide ions, and water molecules.

  10. The effect of oxygen on void stability in ion-irradiated steel

    NASA Astrophysics Data System (ADS)

    Seitzman, Larry E.; Dodd, R. Arthur; Kulcinski, Gerald L.

    1990-07-01

    The effect of oxygen on void stability in an Fe-17Ni-13Cr austenitic ternary alloy has been investigated using 15 MeV nickel-ion irradiation at elevated temperatures and preimplantation of 6 MeV oxygen at room temperature. The nickel irradiation was performed over a temperature range of 550 °C to 650 °C. Utilizing transverse specimen preparation techniques, the irradiated steel was examined by transmission electron microscopy (TEM). As little as 10 appm preimplanted oxygen caused a significant increase in the void number density when the steel was irradiated at 550 °C. A near-surface void-denuded zone occurs in the irradiated steel, while a region depleted of visible voids also occurs in the steel injected with 300 appm oxygen or greater and irradiated at 550 °C.

  11. A New Radio Frequency Plasma Oxygen Primary Ion Source on Nano Secondary Ion Mass Spectrometry for Improved Lateral Resolution and Detection of Electropositive Elements at Single Cell Level.

    PubMed

    Malherbe, Julien; Penen, Florent; Isaure, Marie-Pierre; Frank, Julia; Hause, Gerd; Dobritzsch, Dirk; Gontier, Etienne; Horréard, François; Hillion, François; Schaumlöffel, Dirk

    2016-07-19

    An important application field of secondary ion mass spectrometry at the nanometer scale (NanoSIMS) is the detection of chemical elements and, in particular, metals at the subcellular level in biological samples. The detection of many trace metals requires an oxygen primary ion source to allow the generation of positive secondary ions with high yield in the NanoSIMS. The duoplasmatron oxygen source is commonly used in this ion microprobe but cannot achieve the same quality of images as the cesium primary ion source used to produce negative secondary ions (C(-), CN(-), S(-), P(-)) due to a larger primary ion beam size. In this paper, a new type of an oxygen ion source using a rf plasma is fitted and characterized on a NanoSIMS50L. The performances of this primary ion source in terms of current density and achievable lateral resolution have been characterized and compared to the conventional duoplasmatron and cesium sources. The new rf plasma oxygen source offered a net improvement in terms of primary beam current density compared to the commonly used duoplasmatron source, which resulted in higher ultimate lateral resolutions down to 37 nm and which provided a 5-45 times higher apparent sensitivity for electropositive elements. Other advantages include a better long-term stability and reduced maintenance. This new rf plasma oxygen primary ion source has been applied to the localization of essential macroelements and trace metals at basal levels in two biological models, cells of Chlamydomonas reinhardtii and Arabidopsis thaliana. PMID:27291826

  12. Preferential heating of oxygen 5+ ions by finite-amplitude oblique Alfvén waves

    NASA Astrophysics Data System (ADS)

    Maneva, Yana G.; Viñas, Adolfo; Araneda, Jaime; Poedts, Stefaan

    2016-03-01

    Minor ions in the fast solar wind are known to have higher temperatures and to flow faster than protons in the interplanetary space. In this study we combine previous research on parametric instability theory and 2.5D hybrid simulations to study the onset of preferential heating of Oxygen 5+ ions by large-scale finite-amplitude Alfvén waves in the collisionless fast solar wind. We consider initially non-drifting isotropic multi-species plasma, consisting of isothermal massless fluid electrons, kinetic protons and kinetic Oxygen 5+ ions. The external energy source for the plasma heating and energization are oblique monochromatic Alfvén-cyclotron waves. The waves have been created by rotating the direction of initial parallel pump, which is a solution of the multi-fluid plasma dispersion relation. We consider propagation angles θ ≤ 30°. The obliquely propagating Alfvén pump waves lead to strong diffusion in the ion phase space, resulting in highly anisotropic heavy ion velocity distribution functions and proton beams. We discuss the application of the model to the problems of preferential heating of minor ions in the solar corona and the fast solar wind.

  13. Effect of low energy oxygen ion beam irradiation on ionic conductivity of solid polymer electrolyte

    SciTech Connect

    Manjunatha, H. Kumaraswamy, G. N.; Damle, R.

    2014-04-24

    Over the past three decades, solid polymer electrolytes (SPEs) have drawn significant attention of researchers due to their prospective commercial applications in high energy-density batteries, electrochemical sensors and super-capacitors. The optimum conductivity required for such applications is about 10{sup −2} – 10{sup −4} S/cm, which is hard to achieve in these systems. It is known that the increase in the concentration of salt in the host polymer results in a continuous increase in the ionic conductivity. However, there is a critical concentration of the salt beyond which the conductivity decreases due to formation of ion pairs with no net charge. In the present study, an attempt is made to identify the concentration at which ion pair formation occurs in PEO: RbBr. We have attempted to modify microstructure of the host polymer matrix by low energy ion (Oxygen ion, O{sup +1} with energy 100 keV) irradiation. Ionic conductivity measurements in these systems were carried out using Impedance Spectroscopy before and after irradiation to different fluencies of the oxygen ion. It is observed that the conductivity increases by one order in magnitude. The increase in ionic conductivity may be attributed to the enhanced segmental motion of the polymer chains. The study reveals the importance of ion irradiation as an effective tool to enhance conductivity in SPEs.

  14. Effect of low energy oxygen ion beam irradiation on ionic conductivity of solid polymer electrolyte

    NASA Astrophysics Data System (ADS)

    Manjunatha, H.; Kumaraswamy, G. N.; Damle, R.

    2014-04-01

    Over the past three decades, solid polymer electrolytes (SPEs) have drawn significant attention of researchers due to their prospective commercial applications in high energy-density batteries, electrochemical sensors and super-capacitors. The optimum conductivity required for such applications is about 10-2 - 10-4 S/cm, which is hard to achieve in these systems. It is known that the increase in the concentration of salt in the host polymer results in a continuous increase in the ionic conductivity. However, there is a critical concentration of the salt beyond which the conductivity decreases due to formation of ion pairs with no net charge. In the present study, an attempt is made to identify the concentration at which ion pair formation occurs in PEO: RbBr. We have attempted to modify microstructure of the host polymer matrix by low energy ion (Oxygen ion, O+1 with energy 100 keV) irradiation. Ionic conductivity measurements in these systems were carried out using Impedance Spectroscopy before and after irradiation to different fluencies of the oxygen ion. It is observed that the conductivity increases by one order in magnitude. The increase in ionic conductivity may be attributed to the enhanced segmental motion of the polymer chains. The study reveals the importance of ion irradiation as an effective tool to enhance conductivity in SPEs.

  15. Comparison of oxygen ion outflow on Earth and Mars during space weather events

    NASA Astrophysics Data System (ADS)

    Wei, Y.; Fraenz, M.; Dubinin, E.; Barabash, S.; Dandouras, I. S.; Lundin, R. N.

    2012-12-01

    Solar wind controls non-thermal escape of planetary atmospheric volatiles, regardless of the strength of planetary magnetic fields. For both Earth with a strong dipole and Mars with weak remnant fields, the oxygen ion (O+) outflow has been separately found to be enhanced during corotating interaction region (CIR) passage. To discern the role of terrestrial dipole in protecting planetary volatiles, here for the first time, we compared the enhancements of O+ outflow on Earth and Mars to a CIR which passed by in January, 2008 when Sun, Earth and Mars were approximately aligned. The CIR propagation was recorded by STEREO, ACE, Cluster and Mars Express (MEX). During the CIR passage, Cluster observed enhanced flux of upwelling oxygen ions above the Earth's polar region, while MEX detected increased escape flux of oxygen ions in the Martian magnetosphere. We found that, under a solar wind dynamic pressure increase by 2-3 nPa, the rate of increase in Martian O+ outflow flux was one order higher than those on Earth, thus the dipole effectively prevents coupling of solar wind kinetic energy to planetary ions. Surprisingly, as response to the same part of the CIR body, the rate of increase in Martian O+ outflow flux was on the same order as for Earth. We suggest that, besides existence of a dipole field, the distance to the Sun is also crucially important for planetary volatile loss in our inner solar system.

  16. Reactive Oxygen-Doped 3D Interdigital Carbonaceous Materials for Li and Na Ion Batteries.

    PubMed

    Fan, Ling; Lu, Bingan

    2016-05-01

    Carbonaceous materials as anodes usually exhibit low capacity for lithium ion batteries (LIBs) and sodium ion batteries (SIBs). Oxygen-doped carbonaceous materials have the potential of high capacity and super rate performance. However, up to now, the reported oxygen-doped carbonaceous materials usually exhibit inferior electrochemical performance. To overcome this problem, a high reactive oxygen-doped 3D interdigital porous carbonaceous material is designed and synthesized through epitaxial growth method and used as anodes for LIBs and SIBs. It delivers high reversible capacity, super rate performance, and long cycling stability (473 mA h g(-1) after 500 cycles for LIBs and 223 mA h g(-1) after 1200 cycles for SIBs, respectively, at the current density of 1000 mA g(-1) ), with a capacity decay of 0.0214% per cycle for LIBs and 0.0155% per cycle for SIBs. The results demonstrate that constructing 3D interdigital porous structure with reactive oxygen functional groups can significantly enhance the electrochemical performance of oxygen-doped carbonaceous material.

  17. Method for modifying trigger level for adsorber regeneration

    DOEpatents

    Ruth, Michael J.; Cunningham, Michael J.

    2010-05-25

    A method for modifying a NO.sub.x adsorber regeneration triggering variable. Engine operating conditions are monitored until the regeneration triggering variable is met. The adsorber is regenerated and the adsorbtion efficiency of the adsorber is subsequently determined. The regeneration triggering variable is modified to correspond with the decline in adsorber efficiency. The adsorber efficiency may be determined using an empirically predetermined set of values or by using a pair of oxygen sensors to determine the oxygen response delay across the sensors.

  18. Raising the cycling stability of aqueous lithium-ion batteries by eliminating oxygen in the electrolyte.

    PubMed

    Luo, Jia-Yan; Cui, Wang-Jun; He, Ping; Xia, Yong-Yao

    2010-09-01

    Aqueous lithium-ion batteries may solve the safety problem associated with lithium-ion batteries that use highly toxic and flammable organic solvents, and the poor cycling life associated with commercialized aqueous rechargeable batteries such as lead-acid and nickel-metal hydride systems. But all reported aqueous lithium-ion battery systems have shown poor stability: the capacity retention is typically less than 50% after 100 cycles. Here, the stability of electrode materials in an aqueous electrolyte was extensively analysed. The negative electrodes of aqueous lithium-ion batteries in a discharged state can react with water and oxygen, resulting in capacity fading upon cycling. By eliminating oxygen, adjusting the pH values of the electrolyte and using carbon-coated electrode materials, LiTi(2)(PO(4))(3)/Li(2)SO(4)/LiFePO(4) aqueous lithium-ion batteries exhibited excellent stability with capacity retention over 90% after 1,000 cycles when being fully charged/discharged in 10 minutes and 85% after 50 cycles even at a very low current rate of 8 hours for a full charge/discharge offering an energy storage system with high safety, low cost, long cycling life and appropriate energy density.

  19. Removal of zinc(II) ion by graphene oxide (GO) and functionalized graphene oxide-glycine (GO-G) as adsorbents from aqueous solution: kinetics studies

    NASA Astrophysics Data System (ADS)

    Najafi, F.

    2015-05-01

    The main purpose of this study is to explain the absorption of zinc from aqueous solution by grapheme oxide and functionalized grapheme oxide with glycine as the adsorbent surface. For confirmed functionalized graphene oxide, the glycine amino group was added to the surface of graphene oxide. The effects of the initial concentration of Zn(II) ions and contact time were studied. Results showed that with increasing initial concentration of Zn(II) ions, the adsorption capacity increased. The adsorption capacity did not show a large change after 50 min; therefore, for the study of kinetic parameters, the optimal time of 50 min was selected. The chemical structure of graphene oxide was confirmed by using FT-IR analysis. The adsorption process of Zn(II) ions graphene oxide and functionalized graphene oxide-glycine surfaces was fixed at 298 K and pH 6. The pseudo-first-order and the pseudo-second-order (types I, II, III and IV) kinetic models were tested for the adsorption process and the results showed that the kinetic parameters best fit type (I) of the pseudo-second-order model. A high R 2 was used to be the best match.

  20. Optical planar waveguide in magnesium aluminate spinel crystal using oxygen ion implantation

    NASA Astrophysics Data System (ADS)

    Song, Hong-Lian; Yu, Xiao-Fei; Zhang, Lian; Wang, Tie-Jun; Qiao, Mei; Liu, Peng; Zhao, Jin-Hua; Wang, Xue-Lin

    2015-07-01

    A planar optical waveguide in MgAl2O4 crystal sample was fabricated using 6.0 MeV oxygen ion implantation at a fluence of 1.5 × 1015 ions/cm2 at room temperature. The optical modes were measured at a wavelength of 633 nm using a model 2010 prism coupler. The near-field intensity files in the visible band were measured and simulated with end-face coupling and FD-BPM methods, respectively. The absorption spectra show that the implantation process has almost no effect on the visible and near-infrared band absorption.

  1. Magnetic adsorbent of Fe3O4@SiO2 core-shell nanoparticles modified with thiol group for chloroauric ion adsorption

    NASA Astrophysics Data System (ADS)

    Roto, Roto; Yusran, Yusran; Kuncaka, Agus

    2016-07-01

    The magnetic adsorbent of Fe3O4@SiO2 core-shell nanoparticles modified with thiol group was synthesized for chloroauric ([AuCl4]-) adsorption. The Fe3O4 nanoparticles were prepared by co-precipitation method under mechanical stirring and coated with SiO2 by acid hydrolysis of Na2SiO3 under N2 purging. The coating of Fe3O4 nanoparticles with SiO2 prevents particles' agglomeration by forming Fe3O4 Fe3O4 Fe3O4@SiO2 core-shell and avoids dissolution of the Fe3O4 core in the acidic medium. The coated Fe3O4 particle was modified with a thiol group using 3-mercaptopropyltrimethoxysilane via silanization reaction. The results suggest that SiO2-coated Fe3O4 particles have a size of 10-20 nm. The FTIR and EDX data indicate that the thiol groups are successfully attached to the surface of the nanoparticles. The [AuCl4]- ion adsorption by the Fe3O4@SiO2 core-shell nanoparticles followed Langmuir isotherm model with a maximum adsorption capacity of 115 mg/g and free energy (ΔG°) of 24.8 kJ/mol. The thiourea solution can be used to desorb most of the adsorbed [AuCl4]- ion. The adsorption using magnetic compounds provides easy access to the separation for both preparation and recovery.

  2. Laboratory degradation of Kapton in a low energy oxygen ion beam

    NASA Technical Reports Server (NTRS)

    Ferguson, D. C.

    1984-01-01

    An atomic oxygen ion beam, accelerated from a tunable microwave resonant cavity, was used at Lewis Research Center to bombard samples of the widely used polyimide Kapton. The Kapton experienced degradation and mass loss at high rates, which may be comparable to those found in Space Shuttle operations if the activation energy supplied by the beam enabled surface reactions with the ambient oxygen. The simulation reproduced the directionality (ram-wake dependence) of the degradation, the change in optical properties of the degraded materials, and the structure seen in scanning electron micrographs of samples returned on the Shuttle Trails with a substituted argon ion beam produced no rapid degradation. Energy Dispersive X-ray Analysis (EDAX) showed significant surface composition changes in all bombarded samples. Mass loss rates and surface composition changes are discussed in terms of the possible oxidation chemistry of the interaction. Finally, the question of how the harmful degradation of materials in low Earth orbit can be minimized is addressed.

  3. Laboratory degradation of Kapton in a low energy oxygen ion beam

    NASA Technical Reports Server (NTRS)

    Ferguson, D. C.

    1983-01-01

    An atomic oxygen ion beam, accelerated from a tunable microwave resonant cavity, was used at Lewis Research Center to bombard samples of the widely used polyimide Kapton. The Kapton experienced degradation and mass loss at high rates, which may be comparable to those found in Space Shuttle operations if the activation energy supplied by the beam enabled surface reactions with the ambient oxygen. The simulation reproduced the directionality (ram-wake dependence) of the degradiation, the change in optical properties of the degraded materials, and the structure seen in scanning electron micrographs of samples returned on the Shuttle Trails with a substituted argon ion beam produced no rapid degradation. Energy Dispersive X-ray Analysis (EDAX) showed significant surface composition changes in all bombarded samples. Mass loss rates and surface composition changes are discussed in terms of the possible oxidation chemistry of the interaction. Finally, the question of how the harmful degradation of materials in low earth orbit can be minimized is addressed.

  4. Deeper and earlier penetrations of oxygen ions than protons into the inner magnetosphere Observed by Van Allen probes.

    NASA Astrophysics Data System (ADS)

    Mitani, K.; Seki, K.; Keika, K.; Lanzerotti, L. J.; Gkioulidou, M.; Mitchell, D. G.; Kletzing, C.

    2015-12-01

    It is observationally known that proton and oxygen ions are main components of the ring current during magnetic storms and that the proton and oxygen ions are considered to have different source and supply mechanisms. However, detailed properties of the ion supply and their dependence on ion species is far from well understood. To characterize the ion supply to the ring current during magnetic storms, we report studies of the properties of energetic proton and oxygen ion phase space densities (PSDs) during the April 23-25, 2013, geomagnetic storm observed by the Van Allen Probes mission. We used energetic ion (~50 - ~600keV protons, ~140 - ~1100keV oxygen) and magnetic field data obtained by the RBSPICE and EMFISIS, respectively, on the Van Allen Probes. We calculated ion PSDs for the specific first adiabatic invariant, mu (0.3 < mu < 12 keV/nT), and ion pitch angles near 90 degrees as a function of L for each spacecraft orbit. The results show that both proton and oxygen ions penetrated directly to L<5 during the main phase of the magnetic storm. Protons with smaller mu values (mu = 0.3 and 0.5 keV/nT) penetrated earlier than those with larger mu values (mu = 1.0 keV/nT). This result appears consistent with the energy dependence of the Alfven layer. The timing of oxygen ion penetration is approximately the same for all mu values (mu = 0.8, 1.0 and 1.2 keV/nT). The observations also show that oxygen ions penetrated more deeply in L and earlier in time than protons for the same mu value (mu = 1.0keV/nT). These results suggest that the source of the transported oxygen ions is located closer to the Earth than the inner edge of protons. The results imply the importance of the contribution from subauroral oxygen ions to the storm-time ring current. We will also discuss the possibility of non-adiabatic acceleration of oxygen ions in the inner magnetosphere.

  5. Adsorbents/ion exchangers-PVA blend membranes: Preparation, characterization and performance for the removal of Zn2+ by electrodialysis

    NASA Astrophysics Data System (ADS)

    Caprarescu, Simona; Radu, Anita-Laura; Purcar, Violeta; Ianchis, Raluca; Sarbu, Andrei; Ghiurea, Marius; Nicolae, Cristian; Modrogan, Cristina; Vaireanu, Danut-Ionel; Périchaud, Alain; Ebrasu, Daniela-Ion

    2015-02-01

    The present paper was aimed at studying the possibility of zinc (Zn) removal from the wastewater discharged from zinc electroplating processes. In order to save industrial and environmental resources, the concentrated solution could be reused after electrodialysis process. A mini-electrodialysis system with three cylindrical compartments and different membranes containing various resins (Purolite A500 and Hypersol-Macronet MN500) was employed, which can be further applied for the treatment of synthetic effluent which contained zinc ions. The electrodialysis system was operated at constant voltage using different concentrations of synthetic solutions of zinc ions, without and with electrolyte recirculation for 1.5 h. The pH and conductivity of solutions were measured before and after the electrodialysis process occurs. Also the removal ratio (Rr) and mass flow (J) of zinc ions, energy consumption (EC) and current efficiency (CE) were determined. It was found that electrodialysis treatment generated a very low conductivity solution, enabling its reuse as rinse water. According to the obtained results when using a membrane pair with higher ion exchange capacity (IEC) the removal ratio is improved (over 80%). The physico-chemical, structural and mechanical properties of prepared membranes were registered, before and after electrodialysis process takes place, by means of complementary analytical techniques, namely, ion-exchange capacity, water content and thickness measurements. Furthermore analysis were also carried out by Fourier transform infrared spectroscopy (FT-IR), environmental scanning electron microscopy (ESEM), thermal gravimetric analysis (TGA) and electrochemical impedance spectroscopy (EIS).

  6. An investigation of electron and oxygen ion damage in Si npn RF power transistors

    NASA Astrophysics Data System (ADS)

    Pushpa, N.; Gnana Prakash, A. P.; Praveen, K. C.; Cressler, John D.; Revannasiddaiah, D.

    The effects of 8 MeV electrons and 60 and 95 MeV oxygen ions on the electrical properties of Si npn RF power transistors have been investigated as a function of fluence. The dc current gain (hFE), displacement damage factor, excess base current (Δ IB=IBpost-IBpre), excess collector current (Δ IC=ICpost-ICpre), collector saturation current (ICS) and deep level transient spectroscopy trap signatures of the irradiated transistors were systematically evaluated.

  7. Characterization of Adsorbed Alkali Metal Ions in 2:1 Type Clay Minerals from First-Principles Metadynamics.

    PubMed

    Ikeda, Takashi; Suzuki, Shinichi; Yaita, Tsuyoshi

    2015-07-30

    Adsorption states of alkali metal ions in three kinds of 2:1 type clay minerals are systematically investigated via first-principles-based metadynamics. Our reconstructed free energy surfaces in a two-dimensional space of coordination numbers specifically employed as collective variables for describing the interlayer cations show that an inner-sphere (IS) complex is preferentially formed for Cs(+) in the 2:1 type trioctahedral clay minerals with saponite-like compositions, where lighter alkali metal ions show a tendency to form an outer-sphere one instead. The strong preference for an IS complex observed for Cs(+) is found to result partially from the capability of recognizing selectively Cs(+) ions at the basal O atoms with the Lewis basicity significantly enhanced by the isomorphic substitution in tetrahedral sheets.

  8. Oxygen plasma immersion ion implantation treatment to enhance data retention of tungsten nanocrystal nonvolatile memory

    SciTech Connect

    Wang, Jer-Chyi Chang, Wei-Cheng; Lai, Chao-Sung; Chang, Li-Chun; Ai, Chi-Fong; Tsai, Wen-Fa

    2014-03-15

    Data retention characteristics of tungsten nanocrystal (W-NC) memory devices using an oxygen plasma immersion ion implantation (PIII) treatment are investigated. With an increase of oxygen PIII bias voltage and treatment time, the capacitance–voltage hysteresis memory window is increased but the data retention characteristics become degraded. High-resolution transmission electron microscopy images show that this poor data retention is a result of plasma damage on the tunneling oxide layer, which can be prevented by lowering the bias voltage to 7 kV. In addition, by using the elevated temperature retention measurement technique, the effective charge trapping level of the WO{sub 3} film surrounding the W-NCs can be extracted. This measurement reveals that a higher oxygen PIII bias voltage and treatment time induces more shallow traps within the WO{sub 3} film, degrading the retention behavior of the W-NC memory.

  9. Role of Cu-Ion Doping in Cu-α-MnO2 Nanowire Electrocatalysts for the Oxygen Reduction Reaction

    SciTech Connect

    Davis, Danae J.; Lambert, Timothy N.; Vigil, Julian A.; Rodriguez, Mark A.; Brumbach, Michael T.; Coker, Eric N.; Limmer, Steven J.

    2014-07-09

    The role of Cu-ion doping in α-MnO2 electrocatalysts for the oxygen reduction reaction in alkaline electrolyte was investigated. Copper doped α-MnO2 nanowires (Cu-α-MnO2) were prepared with varying amounts of Cu2+ using a solvothermal method. The electrocatalytic dataindicates that Cu-α-MnO2 nanowires have higher terminal current densities, enhanced kinetic rate constants, and improved charge transfer resistances that trend with Cu-content, exceeding values attained by α-MnO2 alone. The observed improvement in catalytic behavior correlates with an increase in Mn3+ content for the Cu-α-MnO2 nanowires. The Mn3+/Mn4+ couple is themediator for the rate-limiting redox driven O2-/OH- exchange. It is proposed that O2 adsorbs viaan axial site (the eg orbital on the Mn3+ d4 ion) at the surface, or at edge defects, of the nanowireand that the increase in covalent nature of the nanowire with Cu-ion doping leads to stabilization of O2 adsorbates and faster rates of reduction. This work is applicable to other manganese oxide electrocatalysts and shows for the first time there is a correlation for manganese oxides between electrocatalytic activity for the ORR in alkaline electrolyte and an increase in Mn3+ character of the oxide.

  10. Characterization of defects in amorphous SiO 2 implanted with oxygen ions

    NASA Astrophysics Data System (ADS)

    Derryberry, S. L.; Weeks, R. A.; Weller, Robert A.; Mendenhall, Marcus

    1991-07-01

    Electron paramagnetic resonance (EPR) spectra of oxygen-implanted high-purity silica at temperatures ranging from 120 to 300 K have been measured at 9.7 GHz. Silica disks 2.0 cm in diameter and 0.1 cm thick were implanted with O + ions at 140 keV with beam currents < 3 mA/cm 2 and doses that ranged from 8 × 10 15to 8 × 10 16ions/cm 2. Paramagnetic defects have been observed, two of which are similar to defects formed by γ-ray irradiation of silica (E' center and the peroxy-radical (POR)). The POR shows several temperature-dependent features while the E' center has a dose-dependent annihilation cross section, as previously reported by Golanski, Devine, and Oberlin [J. Appl. Phys. 56 (1984) 1572]. Implantation of oxygen hinders defect formation of oxygen deficient defects such as the E' center while favoring production of oxygen-excessive defects such as the POR.

  11. Generation of a fast atomic-oxygen beam from O - ions by resonant cavity radiation

    NASA Astrophysics Data System (ADS)

    Stephen, T. M.; Van Zyl, B.; Amme, R. C.

    1996-04-01

    An apparatus has been developed for producing a beam of ground-electronic-state oxygen atoms with energies variable from 4 to 1000 eV with a 1.5 eV FWHM energy distribution. The technique involves extraction of negative ions from a low-voltage gas-discharge source, mass selection of the extracted O- with a Wien-type velocity filter, O- acceleration or deceleration and focusing by electrostatic ion optics, and electron detachment from O- by intracavity laser radiation. A 25 W argon-ion-laser cavity has been extended to include the ion-beam vacuum chamber so that the intracavity radiation intersects the O- ion trajectories normally. Depending on the laser configuration in use, ion-neutralization efficiencies between 5% and 25% have been achieved at 5 eV O- energy. Thus, 5 eV O-atom fluxes of ˜1011 atoms/s (˜1012 atoms/cm2 s) have been achieved for O- currents of ˜10-7 A. The advantages and limitations of the technique are discussed, and preliminary measurements of the secondary-negative-charge production from low-energy O-atom impact on copper and stainless-steel surfaces are presented.

  12. Fabrication of waveguides in Yb:YCOB crystal by MeV oxygen ion implantation

    NASA Astrophysics Data System (ADS)

    Jiao, Yang; Chen, Feng; Wang, Xue-Lin; Wang, Ke-Ming; Wang, Lei; Wang, Liang-Ling; Zhang, Huai-Jin; Lu, Qing-Ming; Ma, Hong-Ji; Nie, Rui

    2007-07-01

    Oxygen ions with energies of 6.0 or 3.0 MeV were implanted into y-cut Yb:YCOB crystals at fluences ranging from 5.0 × 10 13 to 2.0 × 10 15 ions/cm 2 at room temperature, forming optical planar waveguide structures. Dark-mode line spectroscopy was applied at two wavelengths, 633 and 1539 nm, in various excitation configurations, showing strong enhancement of one of the indices ( nx) in the implanted near surface. The nx refractive index profile is reconstructed by a reflectivity calculation method and compared to the ion energy losses profiles deduced from SRIM-code simulation. Moreover, the near-field patterns were imaged by an end-fire coupling arrangement.

  13. Dayside pickup oxygen ion precipitation at Venus and Mars - Spatial distributions, energy deposition and consequences

    NASA Astrophysics Data System (ADS)

    Luhmann, J. G.; Kozyra, J. U.

    1991-04-01

    The fluxes and energy spectra of picked-up planetary O(+) ions incident on the dayside atmospheres of Venus and Mars are calculated. Maps of precipitating ion number flux and energy flux are presented which show the asymmetrical distribution of dayside energy deposition expected from this source. Although the associated heating of the atmosphere and ionosphere is found to be negligible compared to that from the usual sources, backscattered or sputtered neutral oxygen atoms are produced at energies which exceed that needed for escape from the gravitational fields of both planets. These neutral 'winds', driven by pickup ion precipitation, represent a possibly significant loss of atmospheric constituents over the age of the solar system.

  14. Influence of dopant ion on localized relaxation of an oxygen vacancy in stabilized zirconia

    NASA Astrophysics Data System (ADS)

    Ohta, M.; Wigmore, J. K.; Nobugai, K.; Miyasato, T.

    2002-05-01

    It is well known that stabilized zirconia exhibits long-range transport of oxygen ions which gives rise to diffusion relaxation of oxygen vacancies. The internal friction and the change in sound velocity in single-crystal calcia-stabilized zirconia (CSZ) doped with 12 mol % CaO were measured for longitudinal sound waves in the frequency range from 20 Hz to 700 Hz using a vibrating reed technique. In the temperature range from 300 K to 700 K, the relaxation strength exhibits strong anisotropy with respect to the directions of the k vectors. As the frequency increases the internal friction peak and the change in sound velocity shift toward high temperature, and the relaxation strength remains constant. The results show that a smaller number of oxygen vacancies contribute to diffusion relaxation than to localized relaxation, which is attributed to hopping of bound oxygen vacancies within the local structure. Comparison of the results with those reported previously for yttria-stabilized zirconia (YSZ) doped with 9.5 mol % Y2O3, suggests that oxygen vacancies are more strongly bound by the local structure in CSZ than in YSZ.

  15. Modeling of thorium (IV) ions adsorption onto a novel adsorbent material silicon dioxide nano-balls using response surface methodology.

    PubMed

    Kaynar, Ümit H; Şabikoğlu, Israfil; Kaynar, Sermin Çam; Eral, Meral

    2016-09-01

    The silicon dioxide nano-balls (nano-SiO2) were prepared for the adsorption of thorium (IV) ions from aqueous solution. The synthesized silicon dioxide nano-balls were characterized by Scanning Electron Microscopy/Energy Dispersive X-ray, X-ray Diffraction, Fourier Transform Infrared and BET surface area measurement spectroscopy. The effects of pH, concentration, temperature and the solid-liquid ratio on the adsorption of thorium by nano-balls were optimized using central composite design of response surface methodology. The interaction between four variables was studied and modelled. Furthermore, the statistical analysis of the results was done. Analysis of variance revealed that all of the single effects found statistically significant on the sorption of Th(IV). Probability F-values (F=4.64-14) and correlation coefficients (R(2)=0.99 for Th(IV)) indicate that model fit the experimental data well. The ability of this material to remove Th(IV) from aqueous solution was characterized by Langmuir, Freunlinch and Temkin adsorption isotherms. The adsorption capacity of thorium (IV) achieved 188.2mgg(-1). Thermodynamic parameters were determined and discussed. The batch adsorption condition with respect to interfering ions was tested. The results indicated that silicon dioxide nano-balls were suitable as sorbent material for adsorption and recovery of Th(IV) ions from aqueous solutions. PMID:27451112

  16. Modeling of thorium (IV) ions adsorption onto a novel adsorbent material silicon dioxide nano-balls using response surface methodology.

    PubMed

    Kaynar, Ümit H; Şabikoğlu, Israfil; Kaynar, Sermin Çam; Eral, Meral

    2016-09-01

    The silicon dioxide nano-balls (nano-SiO2) were prepared for the adsorption of thorium (IV) ions from aqueous solution. The synthesized silicon dioxide nano-balls were characterized by Scanning Electron Microscopy/Energy Dispersive X-ray, X-ray Diffraction, Fourier Transform Infrared and BET surface area measurement spectroscopy. The effects of pH, concentration, temperature and the solid-liquid ratio on the adsorption of thorium by nano-balls were optimized using central composite design of response surface methodology. The interaction between four variables was studied and modelled. Furthermore, the statistical analysis of the results was done. Analysis of variance revealed that all of the single effects found statistically significant on the sorption of Th(IV). Probability F-values (F=4.64-14) and correlation coefficients (R(2)=0.99 for Th(IV)) indicate that model fit the experimental data well. The ability of this material to remove Th(IV) from aqueous solution was characterized by Langmuir, Freunlinch and Temkin adsorption isotherms. The adsorption capacity of thorium (IV) achieved 188.2mgg(-1). Thermodynamic parameters were determined and discussed. The batch adsorption condition with respect to interfering ions was tested. The results indicated that silicon dioxide nano-balls were suitable as sorbent material for adsorption and recovery of Th(IV) ions from aqueous solutions.

  17. The Effect of Ion Adsorption on Microbial Dissimilatory Iron-Reduction and the Mobility of Adsorbed As(V)

    NASA Astrophysics Data System (ADS)

    Meyer, B. A.; Stillings, L. L.

    2003-12-01

    The effect of varying environmental conditions on the microbial reduction of Fe(III) and the mobility of adsorbed As(V) was investigated by studying the kinetics of reductive dissolution of synthetic, hydrous ferric oxide (HFO) in three batch-reactor experiments. Growth medium, containing HFO as an electron acceptor (EA) and acetate as an electron donor (ED), was dispensed into 500-ml septum sealed serum bottles. Each bottle was inoculated with an enrichment culture (MEC) containing an anaerobic Fe-reducing bacterium obtained from sediments at Milltown Reservoir near Missoula, MT. Each enrichment culture grew for at least 600 hrs and exhibited both exponential and stationary growth. Microbial reduction was monitored by measuring the production of dissolved Fe(II). Total Fe(II) was calculated by applying a Langmuir adsorption model, developed for each growth condition, to the measured dissolved Fe(II). Total Fe(II) production was modeled by: x = Xs(1-e-ket)-[kL(e-ket)]+(kL/ke) where x is the total Fe(II) concentration (mM) at t, ke is the exponential production rate constant (hr-1), Xs is the total Fe(II) concentration (mM) at the time of transition between exponential and stationary growth, t is the time since inoculation minus lag time, and kL is the stationary (linear) production rate constant (mM hr-1). From our experiments we learned that: 1) increasing the concentration of EA from 10-30 mM had no effect on the value of ke, which remained constant at 0.015 hr-1. However, the maximum production rate, Rmax = (ke Xs)+kL, did increase with increasing EA, varying from 0.014-0.031 mM hr-1; 2) increasing the concentration of ED from 10-30 mM had no effect on either ke or Rmax. These values remained constant as ED increased; 3) sorption of As(V) to the EA (in mM ratios of 1:10 and 1:30, As(V):HFO) affected Rmax but not ke. Rmax increased with increasing EA, as observed earlier, but its value was lower than in cultures without arsenic. In the presence of As(V), Rmax was

  18. Dayside pickup oxygen ion precipitation at Venus and Mars: Spatial distributions, energy deposition and consequences

    SciTech Connect

    Luhmann, J.G. ); Kozyra, J.U. )

    1991-04-01

    The fluxes and energy spectra of picked-up planetary O{sup +} ions incident on the dayside atmospheres of Venus and Mars are calculated using the neutral exposure models of Nagy and Cravens (1988) and the Spreiter and Stahara (1980) gasdynamic model of the magnetosheath electric and magnetic field. Cold ({approximately}10 eV) O{sup +} ions are launched from hemispherical grids of starting points covering the daysides of the planets and their trajectories are followed until they either impact the dayside obstacle or cross the terminator plane. The impacting, or precipitating, ion fluxes are weighted according to the altitude of the hemispherical starting point grid in a manner consistent with the exosphere density models and the local photoion production rate. Maps of precipitating ion number flux and energy flux show the asymmetrical distribution of dayside energy deposition expected from this source which is unique to the weakly magnetized planets. Although the associated heating of the atmosphere and ionsphere is found to be negligible compared to that from the usual sources, backscattered or sputtered neutral oxygen atoms are produced at energies exceeding that needed for escape from the gravitational fields of both planets. These neutral winds, driven by pickup ion precipitation, represent a possibly significant loss of atmospheric constituents over the age of the solar system.

  19. Prussian blue caged in alginate/calcium beads as adsorbents for removal of cesium ions from contaminated water.

    PubMed

    Vipin, Adavan Kiliyankil; Hu, Baiyang; Fugetsu, Bunshi

    2013-08-15

    Prussian blue encapsulated in alginate beads reinforced with highly dispersed carbon nanotubes were prepared for the safe removal of cesium ions from aqueous solutions. Equilibrium and kinetic studies were conducted using different models and the goodness of mathematical fitting of the experimental data on the adsorption isotherms was in the order Langmuir>Freundlich, and that of the kinetic models were in the order of pseudo second order>pseudo first order. Fixed bed adsorption column analysis indicated that the beads can be used for large scale treatment of cesium contaminated water.

  20. Mass spectrometry of refractory black carbon particles from six sources: carbon-cluster and oxygenated ions

    NASA Astrophysics Data System (ADS)

    Corbin, J. C.; Sierau, B.; Gysel, M.; Laborde, M.; Keller, A.; Kim, J.; Petzold, A.; Onasch, T. B.; Lohmann, U.; Mensah, A. A.

    2013-10-01

    We discuss the major mass spectral features of different types of refractory carbonaceous particles, ionized after laser vapourization with an Aerodyne High-Resolution Soot-Particle Aerosol Mass Spectrometer (SP-AMS). The SP-AMS was operated with a switchable 1064 nm laser and a 600 °C thermal vapourizer, yielding respective measurements of the refractory and non-refractory particle components. Six samples were investigated, all of which were composed primarily of refractory material: fuel-rich and fuel-lean propane/air diffusion-flame combustion particles; graphite-spark-generated particles; a commercial Fullerene-enriched Soot; Regal Black, a commercial carbon black; and nascent aircraft-turbine combustion particles. All samples exhibited a spectrum of carbon-cluster ions Cxn+ in their refractory mass spectrum. Smaller clusters (x<6) were found to dominate the Cxn+ distribution. For Fullerene Soot, fuel-rich-flame particles and spark-generated particles, significant Cxn+ clusters at x≫6 were present, with significant contributions from multiply-charged ions (n>1). In all six cases, the ions C1+ and C3+ contributed over 60% to the total C1ions C1+/C3+ could be used to predict whether significant Cxn+ signals with x>5 were present. When such signals were present, C1+/C3+ was close to 1. When absent, C1+/C3+ was <0.8. This ratio may therefore serve as a proxy to distinguish between the two types of spectra in atmospheric SP-AMS measurements. Significant refractory oxygenated ions such as CO+ and CO2+ were also observed for all samples. We discuss these signals in detail for Regal Black, and describe their formation via decomposition of oxygenated moieties incorporated into the refractory carbon structure. These species may be of importance in atmospheric processes such as water uptake, aging and heterogeneous chemistry.

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

    PubMed

    Qian, Guofei; Song, Hang; Yao, Shun

    2016-01-15

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

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

    PubMed

    Qian, Guofei; Song, Hang; Yao, Shun

    2016-01-15

    Tropine-type chiral ionic liquid with proline anion was immobilized on silica gel by chemical modification method for the first time, which was proved by elemental, infrared spectrum and thermogravimetric analysis. Secondly, the performance of this kind of ionic liquid-modified silica gel was investigated in the adsorption of some metal ions, which included Cu(2+), Fe(3+), Mn(2+) and Ni(2+). Then the effects of time, initial concentration and temperature on adsorption for Cu(2+) ions were studied in detail, which was followed by the further research of adsorption kinetics and thermodynamics. The adsorption could be better described by pseudo-second-order kinetics model and that the process was spontaneous, exothermic and entropy decreasing. In the mode of 'reuse after adsorption', the ionic liquid-modified silica gel with saturated adsorption of Cu(2+) was finally used in resolution of racemic amino acids for the first time. The static experiment showed that adsorption rate of two enantiomers was obviously different. Inspired by this, the complex was packed in chromatographic column for the separation of racemic amino acids and d-enantiomers were firstly eluted by water or ethanol. Steric hindrance was found as one of key influencing factors for its effect on the stability of the complex. PMID:26711153

  3. Highly selective removal of Zn(II) ion from hot-dip galvanizing pickling waste with amino-functionalized Fe3O4@SiO2 magnetic nano-adsorbent.

    PubMed

    Bao, Shuangyou; Tang, Lihong; Li, Kai; Ning, Ping; Peng, Jinhui; Guo, Huibin; Zhu, Tingting; Liu, Ye

    2016-01-15

    Amino-functionalized Fe3O4@SiO2 magnetic nano-adsorbent was used as a novel sorbent to highly selective removal of Zn(II) ion from hot-dip galvanizing pickling waste in the presence of Fe(II). These hot-dip galvanizing pickling waste mainly contain ZnCl2 and FeCl2 in aqueous HCl media. The properties of this magnetic adsorbent were examined by transmission electron microscopy (TEM), powder X-ray diffraction (XRD), infrared spectrometer (FT-IR) and BET surface area measurements. Various factors influencing the adsorption of Zn(II) ion such as initial concentration of metal ions, the amount of adsorbent, pH value of the solutions, the concentration of coexisting iron ion were investigated by batch experiments. The results indicated that the adsorption equilibrium data obeyed the Freundlich model with maximum adsorption capacities for Zn(II) to 169.5mg/g. The maximum adsorption occurred at pH 5±0.1 and Fe(II) interferences had no obvious influence. This work provides a potential and unique technique for zinc ion removal from hot-dip galvanizing pickling waste. PMID:26458121

  4. Post oxygen treatment characteristics of coke as an anode material for Li-ion batteries.

    PubMed

    Kim, Jae-Hun; Park, Min-Sik; Jo, Yong Nam; Yu, Ji-Sang; Jeong, Goojin; Kim, Young-Jun

    2013-05-01

    The effect of a oxygen treatment on the electrochemical characteristics of a soft carbon anode material for Li-ion batteries was investigated. After a coke carbonization process at 1000 degrees C in an argon atmosphere, the samples were treated under a flow of oxygen gas to obtain a mild oxidation effect. After this oxygen treatment, the coke samples exhibited an improved initial coulombic efficiency and cycle performance as compared to the carbonized sample. High-resolution transmission electron microscopy revealed that the carbonized cokes consisted of disordered and nanosized graphene layers and the surface of the modified carbon was significantly changed after the treatment. The chemical state of the cokes was analyzed using X-ray photoelectron spectroscopy and Fourier transform infrared spectroscopy. The enhanced electrochemical properties of the surface modified cokes could be attributed to the mild oxidation effect induced by the oxygen treatment. The mild oxidation process could have led to the elimination of surface imperfections and the reinforcement of a solid electrolyte interphase film, which resulted in the improved electrochemical characteristics.

  5. Effects of extracellular zinc ion on the rate of oxygen consumption of rat brain mitochondria.

    PubMed

    Kukoyi, B I

    2006-01-01

    The inhibitory effect of extracellular zinc ion on the rate of oxygen consumption of rat brain mitochondria pre-incubated in 1.0 mMol Ca(2+)EDTA were determined. There was a significant increase [P < 0.01] in the rate of oxygen consumption in the rat brain mitochondria pre-incubated in 1.0 mMol Ca(2+)EDTA in a succinate initiated reaction. The reverse was the case when the concentration of Ca(2+)EDTA was increased to 10 mMol. A 20 microMol zinc-aspartate was found to have no inhibitory effect on the rate of oxygen consumption of the brain mitochondria pre-incubated with 1.0 mMol Ca(2+)EDTA when compared with the control that lacked 1.0 mMol Ca(2+)EDTA, however there was a significant decrease [P < 0.01] in the rate of oxygen consumption of the rat brain mitochondria in the control experiment.

  6. Adair-based hemoglobin equilibrium with oxygen, carbon dioxide and hydrogen ion activity.

    PubMed

    Mateják, Marek; Kulhánek, Tomáš; Matoušek, Stanislav

    2015-04-01

    As has been known for over a century, oxygen binding onto hemoglobin is influenced by the activity of hydrogen ions (H⁺), as well as the concentration of carbon dioxide (CO₂). As is also known, the binding of both CO₂and H⁺ on terminal valine-1 residues is competitive. One-parametric situations of these hemoglobin equilibria at specific levels of H⁺, O₂or CO₂are also well described. However, we think interpolating or extrapolating this knowledge into an 'empirical' function of three independent variables has not yet been completely satisfactory. We present a model that integrates three orthogonal views of hemoglobin oxygenation, titration, and carbamination at different temperatures. The model is based only on chemical principles, Adair's oxygenation steps and Van't Hoff equation of temperature dependences. Our model fits the measurements of the Haldane coefficient and CO₂hemoglobin saturation. It also fits the oxygen dissociation curve influenced by simultaneous changes in H⁺, CO₂and O₂, which makes it a strong candidate for integration into more complex models of blood acid-base with gas transport, where any combination of mentioned substances can appear. PMID:25594800

  7. Adair-based hemoglobin equilibrium with oxygen, carbon dioxide and hydrogen ion activity.

    PubMed

    Mateják, Marek; Kulhánek, Tomáš; Matoušek, Stanislav

    2015-04-01

    As has been known for over a century, oxygen binding onto hemoglobin is influenced by the activity of hydrogen ions (H⁺), as well as the concentration of carbon dioxide (CO₂). As is also known, the binding of both CO₂and H⁺ on terminal valine-1 residues is competitive. One-parametric situations of these hemoglobin equilibria at specific levels of H⁺, O₂or CO₂are also well described. However, we think interpolating or extrapolating this knowledge into an 'empirical' function of three independent variables has not yet been completely satisfactory. We present a model that integrates three orthogonal views of hemoglobin oxygenation, titration, and carbamination at different temperatures. The model is based only on chemical principles, Adair's oxygenation steps and Van't Hoff equation of temperature dependences. Our model fits the measurements of the Haldane coefficient and CO₂hemoglobin saturation. It also fits the oxygen dissociation curve influenced by simultaneous changes in H⁺, CO₂and O₂, which makes it a strong candidate for integration into more complex models of blood acid-base with gas transport, where any combination of mentioned substances can appear.

  8. Dynamics of oxygen sorption from water by copper-containing fibrous porous redox ion-exchangers

    SciTech Connect

    Ul'eva, L.S.; Burinskii, S.V.; Grebennikov, S.F.

    1985-08-10

    A most important field of practical application of oxidation-reduction (redox) polymers is the sorption of dissolved oxygen from water in order to prevent corrosion of power equipment. Copper-containing redox polymers, which have fairly high capacity and good swelling characteristics were used. Values of the dynamic exchange capacity (DEC) for copper ions, the redox capacity (ROC) for the reducing metal, and the dynamic reduction capacity for oxygen are given. It can be seen from these data that fibrous porous reactive materials (FPRM) in which the mass fiber content is 60% have somewhat better characteristics. The authors conclude that despite the fibrous porous material's considerably lower coefficient of internal diffusion, it is superior to granular EI-21 in the length of the masstransfer zone and in the coefficient of utilization of capacity, in consequence of the low linear density of the fibers. Their mass transfer zone is shorter by a factor of about 5.

  9. First experimental-based characterization of oxygen ion beam depth dose distributions at the Heidelberg Ion-Beam Therapy Center

    NASA Astrophysics Data System (ADS)

    Kurz, C.; Mairani, A.; Parodi, K.

    2012-08-01

    Over the last decades, the application of proton and heavy-ion beams to external beam radiotherapy has rapidly increased. Due to the favourable lateral and depth dose profile, the superposition of narrow ion pencil beams may enable a highly conformal dose delivery to the tumour, with better sparing of the surrounding healthy tissue in comparison to conventional radiation therapy with photons. To fully exploit the promised clinical advantages of ion beams, an accurate planning of the patient treatments is required. The clinical treatment planning system (TPS) at the Heidelberg Ion-Beam Therapy Center (HIT) is based on a fast performing analytical algorithm for dose calculation, relying, among others, on laterally integrated depth dose distributions (DDDs) simulated with the FLUKA Monte Carlo (MC) code. Important input parameters of these simulations need to be derived from a comparison of the simulated DDDs with measurements. In this work, the first measurements of 16O ion DDDs at HIT are presented with a focus on the determined Bragg peak positions and the understanding of factors influencing the shape of the distributions. The measurements are compared to different simulation approaches aiming to reproduce the acquired data at best. A simplified geometrical model is first used to optimize important input parameters, not known a priori, in the simulations. This method is then compared to a more realistic, but also more time-consuming simulation approach better accounting for the experimental set-up and the measuring process. The results of this work contributed to a pre-clinical oxygen ion beam database, which is currently used by a research TPS for corresponding radio-biological cell experiments. A future extension to a clinical database used by the clinical TPS at HIT is foreseen. As a side effect, the performed investigations showed that the typical water equivalent calibration approach of experimental data acquired with water column systems leads to slight

  10. Including oxygen enhancement ratio in ion beam treatment planning: model implementation and experimental verification.

    PubMed

    Scifoni, E; Tinganelli, W; Weyrather, W K; Durante, M; Maier, A; Krämer, M

    2013-06-01

    We present a method for adapting a biologically optimized treatment planning for particle beams to a spatially inhomogeneous tumor sensitivity due to hypoxia, and detected e.g., by PET functional imaging. The TRiP98 code, established treatment planning system for particles, has been extended for including explicitly the oxygen enhancement ratio (OER) in the biological effect calculation, providing the first set up of a dedicated ion beam treatment planning approach directed to hypoxic tumors, TRiP-OER, here reported together with experimental tests. A simple semi-empirical model for calculating the OER as a function of oxygen concentration and dose averaged linear energy transfer, generating input tables for the program is introduced. The code is then extended in order to import such tables coming from the present or alternative models, accordingly and to perform forward and inverse planning, i.e., predicting the survival response of differently oxygenated areas as well as optimizing the required dose for restoring a uniform survival effect in the whole irradiated target. The multiple field optimization results show how the program selects the best beam components for treating the hypoxic regions. The calculations performed for different ions, provide indications for the possible clinical advantages of a multi-ion treatment. Finally the predictivity of the code is tested through dedicated cell culture experiments on extended targets irradiation using specially designed hypoxic chambers, providing a qualitative agreement, despite some limits in full survival calculations arising from the RBE assessment. The comparison of the predictions resulting by using different model tables are also reported. PMID:23681217

  11. The effect of exogenous zinc ions on the pattern of oxygen consumption of the hepatic mitochondria of albino rats.

    PubMed

    Kukoyi, B I; Costello, L C; Franklin, R B

    2004-12-01

    The effect of incubation of coupled liver mitochondria on varying concentration of zinc ion was determined. A low concentration of 6 microM zinc ion was found to inhibit the rate of oxygen consumption of the liver mitochondria significantly [P < 0.01]. There was uncoupling of the liver mitochondria when subjected to varying incubation periods. There was no change observed in the control experiment. Zinc-citrate inhibited the rate of oxygen consumption significantly [P < 0.01] when compare with the control. The changes observed in the Zn-aspartate were insignificant. Zn-EDTA had no inhibitory or stimulatory effect on the rate of liver mitochondrial oxygen consumption.

  12. Structured back gates for high-mobility two-dimensional electron systems using oxygen ion implantation

    NASA Astrophysics Data System (ADS)

    Berl, M.; Tiemann, L.; Dietsche, W.; Karl, H.; Wegscheider, W.

    2016-03-01

    We present a reliable method to obtain patterned back gates compatible with high mobility molecular beam epitaxy via local oxygen ion implantation that suppresses the conductivity of an 80 nm thick silicon doped GaAs epilayer. Our technique was optimized to circumvent several constraints of other gating and implantation methods. The ion-implanted surface remains atomically flat which allows unperturbed epitaxial overgrowth. We demonstrate the practical application of this gating technique by using magneto-transport spectroscopy on a two-dimensional electron system (2DES) with a mobility exceeding 20 × 106 cm2/V s. The back gate was spatially separated from the Ohmic contacts of the 2DES, thus minimizing the probability for electrical shorts or leakage and permitting simple contacting schemes.

  13. Negative ion clusters in oxygen: collision cross sections and transport coefficients

    NASA Astrophysics Data System (ADS)

    de Urquijo, J.; Bekstein, A.; Ducasse, O.; Ruíz-Vargas, G.; Yousfi, M.; Benhenni, M.

    2009-12-01

    Using a pulsed Townsend experiment, we have observed the formation of two negative ion species in oxygen over the pressure range 100-600 torr, and the density-normalised electric field strength, E/N, from 2 to 14 Td. The peculiar shape of these transients has led us to propose a scheme of three-body ion-molecule reactions leading to the formation of O4 - and O6 -, which is substantiated by a curve fitting procedure. The resulting mobility data of these two ionic species have been used to calculate their respective momentum transfer collision cross sections, together with the dissociation cross sections that are needed to extend the range of calculation of mobility and diffusion (transverse and longitudinal) to 1000 Td. These calculations were based on an optimised Monte Carlo algorithm, using collision cross sections obtained from a JWKB approximation (Jeffreys-Wentzel-Kramers-Brillouin) or taken from literature.

  14. High impact of uranyl ions on carrying-releasing oxygen capability of hemoglobin-based blood substitutes.

    PubMed

    Duan, Li; Du, Lili; Jia, Yi; Liu, Wenyuan; Liu, Zhichao; Li, Junbai

    2015-01-01

    The effect of radioactive UO2 (2+) on the oxygen-transporting capability of hemoglobin-based oxygen carriers has been investigated in vitro. The hemoglobin (Hb) microspheres fabricated by the porous template covalent layer-by-layer (LbL) assembly were utilized as artificial oxygen carriers and blood substitutes. Magnetic nanoparticles of iron oxide (Fe3 O4 ) were loaded in porous CaCO3 particles for magnetically assisted chemical separation (MACS). Through the adsorption spectrum of magnetic Hb microspheres after adsorbing UO2 (2+) , it was found that UO2 (2+) was highly loaded in the magnetic Hb microspheres, and it shows that the presence of UO2 (2+) in vivo destroys the structure and oxygen-transporting capability of Hb microspheres. In view of the high adsorption capacity of UO2 (2+) , the as-assembled magnetic Hb microspheres can be considered as a novel, highly effective adsorbent for removing metal toxins from radiation-contaminated bodies, or from nuclear-power reactor effluent before discharge into the environment.

  15. Influence of Kilo-Electron Oxygen Ion Irradiation on Structural, Electrical and Optical Properties of CdTe Thin Films

    NASA Astrophysics Data System (ADS)

    Honey, Shehla; Thema, F. T.; Bhatti, M. T.; Ishaq, A.; Naseem, Shahzad; Maaza, M.

    2016-09-01

    In this paper, effect of oxygen (O+) ion irradiation on the properties of polycrystalline cubic structure CdTe thin films has been investigated. CdTe thin films were irradiated with O+ ions of energy 80keV at different fluence ranging from 1×1015 to 5×1016 ion/cm2 at room temperature. At 1×1015 ion/cm2 O+ ions fluence, the CdTe structure was maintained while XRD peaks of cubic phase were shifted toward lower angles. At 5×1016 ion/cm2 O+ ions fluence, cubic structure of CdTe thin films was transformed into hexagonal structure. In addition, electrical resistivity and optical bandgap were decreased with increasing O+ ion beam irradiation.

  16. Copper-Exchanged Zeolite L Traps Oxygen

    NASA Technical Reports Server (NTRS)

    Sharma, Pramod K.; Seshan, Panchalam K.

    1991-01-01

    Brief series of simple chemical treatments found to enhance ability of zeolite to remove oxygen from mixture of gases. Thermally stable up to 700 degrees C and has high specific surface area which provides high capacity for adsorption of gases. To increase ability to adsorb oxygen selectively, copper added by ion exchange, and copper-exchanged zeolite reduced with hydrogen. As result, copper dispersed atomically on inner surfaces of zeolite, making it highly reactive to oxygen, even at room temperature. Reactivity to oxygen even greater at higher temperatures.

  17. Using Ion Injections to Infer the Energetic Oxygen and Sulfur Charge States in Jupiter's Inner and Middle Magnetosphere

    NASA Astrophysics Data System (ADS)

    Clark, G. B.; Mauk, B.; Paranicas, C.; Kollmann, P.; Mitchell, D. G.

    2015-12-01

    Neutral gases can, through the charge exchange processes, shape the distributions of energetic ions trapped within a planetary magnetosphere, and also redistribute the energetic ion charge states. One region where the prevalence of such processes has been proposed is the orbital region of Jupiter's moon Europa, where the existence of a neutral gas torus has been inferred. Data from the Galileo Energetic Particle Detector (EPD) showed a depletion of protons with near equatorial pitch angles near Europa, while oxygen and sulfur maintained their trapped profile as they were transported inward. The contrast in these distributions was attributed by Lagg et al. (2003) to the multiple charge states of the oxygen and sulfur, dramatically increasing the charge exchange lifetimes of these species. It was proposed that as the ions diffuse inwards across Europa's orbit and into the Io torus regions, the distributed neutral gas interactions redistribute the charge states of the heavy ions until, close to Io, these ions may be heavily depleted. And so, the charge state of the heavy ions is a critical parameter in determining whether or not these processes are taking place. Limited evidence for the multiple charged states of heavy ions was provided by Mauk et al. [1999], who analyzed three ion injection events and found evidence of multiply charged energetic oxygen and sulfur ions in two of the events, but not in the third event. Injections introduce a transient disturbance to the ion distributions, and the drift rate of disturbed ions away from the injection region depends on the charge state of the ions. In this work we revisit the Galileo EPD data set and find additional ion dispersion events from which composition can be measured and charge state can be inferred. We aspire to develop a much clearer picture as to the ordering of charge state as a function of radial distance. Results and conclusions will be presented as well as the importance from new measurements from the

  18. Influence of Oxygen Ion Implantation on the Damage and Annealing Kinetics of Iron-Implanted Sapphire

    SciTech Connect

    Hunn, J.D.; McHargue, C.J.

    1999-11-14

    The effects of implanted oxygen on the damage accumulation in sapphire which was previously implanted with iron was studied for (0001) sapphire implanted with iron and then with oxygen. The energies were chosen to give similar projected ranges. One series was implanted with a 1:l ratio (4x10{sup 16} ions/cm{sup 2} each) and another with a ratio of 2:3 (4x10{sup 16} fe{sup +}/cm{sup 2}; 6x10{sup 16} O{sup +}/cm{sup 2}). Retained damage, X, in the Al-sublattice, was compared to that produced by implantation of iron alone. The observed disorder was less for the dual implantations suggesting that implantation of oxygen enhanced dynamic recovery during implantation. Samples were annealed for one hour at 800 and 1200 C in an oxidizing and in a reducing atmosphere. No difference was found in the kinetics of recovery in the Al-sublattice between the two dual implant conditions. However, the rate of recovery was different for each from samples implanted with iron alone.

  19. Mass spectrometry of refractory black carbon particles from six sources: carbon-cluster and oxygenated ions

    NASA Astrophysics Data System (ADS)

    Corbin, J. C.; Sierau, B.; Gysel, M.; Laborde, M.; Keller, A.; Kim, J.; Petzold, A.; Onasch, T. B.; Lohmann, U.; Mensah, A. A.

    2014-03-01

    We discuss the major mass spectral features of different types of refractory carbonaceous particles, ionized after laser vaporization with an Aerodyne high-resolution soot-particle aerosol mass spectrometer (SP-AMS). The SP-AMS was operated with a switchable 1064 nm laser and a 600 °C thermal vaporizer, yielding respective measurements of the refractory and non-refractory particle components. Six samples were investigated, all of which were composed primarily of refractory material: fuel-rich and fuel-lean propane/air diffusion-flame combustion particles; graphite-spark-generated particles; a commercial fullerene-enriched soot; Regal Black, a commercial carbon black; and nascent aircraft-turbine combustion particles. All samples exhibited a spectrum of carbon-cluster ions Cxn+ in their refractory mass spectrum. Smaller clusters (x < 6) were found to dominate the Cxn+ distribution. For fullerene soot, fuel-rich-flame particles and spark-generated particles, significant Cxn+ clusters at x ≫ 6 were present, with significant contributions from multiply charged ions (n > 1). In all six cases, the ions C1+ and C3+ contributed over 60% to the total C1ions C1+ / C3+ could be used to predict whether significant Cxn+ signals with x > 5 were present. When such signals were present, C1+ / C3+ was close to 1. When absent, C1+ / C3+ was < 0.8. This ratio may therefore serve as a proxy to distinguish between the two types of spectra in atmospheric SP-AMS measurements. Significant refractory oxygenated ions such as CO+ and CO2+ were also observed for all samples. We discuss these signals in detail for Regal Black, and describe their formation via decomposition of oxygenated moieties incorporated into the refractory carbon structure. These species may be of importance in atmospheric processes such as water uptake and heterogeneous chemistry. If atmospherically stable, these oxidized species may be useful for distinguishing

  20. The influence of negative ions in helium-oxygen barrier discharges: I. Laser photodetachment experiment

    NASA Astrophysics Data System (ADS)

    Tschiersch, R.; Nemschokmichal, S.; Meichsner, J.

    2016-04-01

    This work is the experimental part of a comprehensive study that aims to understand the influence of negative ions on the development of atmospheric pressure barrier discharges in electronegative systems. The investigations will be complemented by a 1D numerical fluid simulation. Laser photodetachment experiments were performed in a glow-like barrier discharge operated in helium with admixtures of oxygen up to 1 vol.% at a gas pressure of 500 mbar. The discharge gap between the glass-coated electrodes was 3 mm. The discharge properties were characterized by electrical measurements and optical emission spectroscopy. Laser photodetachment of {{\\text{O}}-} , {\\text{O}}2- , and {\\text{O}}3- was studied using the fundamental and second harmonic wavelength of a Nd-YAG laser. The laser photodetachment of negative ions influences the breakdown characteristics when the laser is fired during the prephase of the discharge only. The breakdown voltage is reduced, which indicates an enhanced pre-ionization initiated by the detached electrons. Systematic variations in the laser pulse in time, the axial laser beam position, the laser pulse energy, and the laser wavelength provided detailed knowledge on this process. The investigation underlines the importance of the discharge prephase in general and aims to differentiate between the negative ion species {{\\text{O}}-} , {\\text{O}}2- , and {\\text{O}}3- .

  1. Experimental study of electric dipoles on an oxygen-adsorbed Si(100)-2 × 1 surface by non-contact scanning nonlinear dielectric microscopy

    SciTech Connect

    Suzuki, Masataka; Yamasue, Kohei Cho, Yasuo

    2015-07-20

    Oxygen-adsorption on a Si(100)-2 × 1 surface is investigated by using non-contact scanning nonlinear dielectric microscopy (NC-SNDM). On the Si(100)-2 × 1 surface exposed to oxygen (O{sub 2}) gas at room temperature, several variations in atomic configuration and electric dipole moment of dimers are observed. Models are proposed for oxygen adsorption which are consistent with the topographies and electric dipole moment distributions obtained by NC-SNDM.

  2. Hydraulic Permeability of Resorcinol-Formaldehyde Ion-Exchange Resin - Effects of Oxygen Uptake and Radiation

    SciTech Connect

    Taylor, Paul Allen

    2009-01-01

    An ion-exchange process, using spherical resorcinol-formaldehyde (RF) resin is the baseline process for removing cesium from the dissolved salt solution in the high-level waste tanks at the U.S. Department of Energy's (DOE) Hanford site in Washington State. The RF resin is also being evaluated for use in the proposed Small Column Ion Exchange (SCIX) system, which is an alternative treatment option at DOE's Savannah River Site (SRS)in South Carolina. Testing at ORNL will determine the impact of radiation exposure and oxygen uptake by the RF resin on the hydraulic permeability of the resin. Samples of the resin will be removed periodically to measure physical properties (bead size and compressibility) and cesium capacity. The proposed full-scale treatment system at Hanford, the Waste Treatment Plant (WTP), will use an ion-exchange column containing nominally 680 gal of resin, which will treat 30 gpm of waste solution. The ion-exchange column is designed for a typical pressure drop of 6 psig, with a maximum of 9.7 psig. The lab-scale column is 3-in. clear PVC pipe and is prototypic of the proposed Hanford column. The fluid velocity in the lab-scale test will be much higher than for the full-scale column, in order to generate the maximum pressure drop expected in that column (9.7 psig). The frictional drag from this high velocity will produce similar forces on the resin in the lab-scale column as would be expected at the bottom of the full-scale column. The chemical changes in the resin caused by radiation exposure and oxygen uptake are expected to cause physical changes in the resin that could reduce the bed porosity and reduce the hydraulic permeability of the resin bed. These changes will be monitored by measuring the pressure drop through the lab-scale column and by measuring the physical properties of samples of the resin. The test loop with the lab-scale column is currently being fabricated, and operation will start by late May. Testing will be completed by the

  3. Correlation between structure and oxygen ion dynamics in Y substituted La2Mo2O9 ionic conductors

    NASA Astrophysics Data System (ADS)

    Paul, T.; Ghosh, A.

    2016-09-01

    We have measured the ac conductivity and dielectric spectra for La2-xYxMo2O9 (0.05 ≤ x ≤ 0.20) in wide temperature and frequency ranges. We have obtained the mean square displacement and the spatial extent of nonrandom sub-diffusive regions for oxygen ions by analyzing the ac conductivity and dielectric spectra respectively. The structure of the samples has been studied using X-ray photoelectron spectra, X-ray and electron diffraction. It is observed that the composition dependence of these characteristic lengths is correlated with the distance between oxygen ions obtained from structural studies.

  4. Search for free quarks produced by 14. 5-GeV/nucleon oxygen ions

    SciTech Connect

    Shaw, G.L.; Matis, H.S.; Pugh, H.G.; Slansky, R.; Alba, G.P.; Bland, R.W.; Dickson, S.C.; Hodges, C.L.; Johnson, R.T.; Lindgren, M.A.

    1987-12-01

    A high-sensitivity experiment was carried out to detect free quarks produced in collisions of 14.5-GeV/nucleon oxygen nuclei with a heavy target at BNL. Secondaries from the collisions were stopped in liquid-argon tanks, and charged atoms were collected electrostatically on gold-coated electrodes. The gold coatings were dissolved in a small drop of mercury, which was then tested for quarks in the San Francisco State University automated Millikan apparatus. No evidence for free fractional charge was found. The resulting upper limit is less than 1.0 x 10/sup -9/ quarks produced per incident /sup 16/O ion at 90% C.L.

  5. Light-ion production in the interaction of 96 MeV neutrons with oxygen

    SciTech Connect

    Tippawan, U.; Pomp, S.; Atac, A.; Blomgren, J.; Dangtip, S.; Hildebrand, A.; Johansson, C.; Klug, J.; Mermod, P.; Oesterlund, M.; Bergenwall, B.; Nilsson, L.; Olsson, N.; Prokofiev, A.V.; Nadel-Turonski, P.; Corcalciuc, V.; Koning, A.J.

    2006-03-15

    Double-differential cross sections are reported for light-ion (p, d, t, {sup 3}He, and {alpha}) production in oxygen induced by 96 MeV neutrons. Energy spectra are measured at eight laboratory angles from 20 degree sign to 160 degree sign in steps of 20 degree sign . Procedures for data taking and data reduction are presented. Deduced energy-differential and production cross sections are reported. Experimental cross sections are compared to theoretical reaction model calculations and experimental data at lower neutron energies in the literature. The measured proton data agree reasonably well with the results of the model calculations, whereas the agreement for the other particles is less convincing. The measured production cross sections for protons, deuterons, tritons, and {alpha} particles support the trends suggested by data at lower energies.

  6. In situ stress observation in oxide films and how tensile stress influences oxygen ion conduction

    PubMed Central

    Fluri, Aline; Pergolesi, Daniele; Roddatis, Vladimir; Wokaun, Alexander; Lippert, Thomas

    2016-01-01

    Many properties of materials can be changed by varying the interatomic distances in the crystal lattice by applying stress. Ideal model systems for investigations are heteroepitaxial thin films where lattice distortions can be induced by the crystallographic mismatch with the substrate. Here we describe an in situ simultaneous diagnostic of growth mode and stress during pulsed laser deposition of oxide thin films. The stress state and evolution up to the relaxation onset are monitored during the growth of oxygen ion conducting Ce0.85Sm0.15O2-δ thin films via optical wafer curvature measurements. Increasing tensile stress lowers the activation energy for charge transport and a thorough characterization of stress and morphology allows quantifying this effect using samples with the conductive properties of single crystals. The combined in situ application of optical deflectometry and electron diffraction provides an invaluable tool for strain engineering in Materials Science to fabricate novel devices with intriguing functionalities. PMID:26912416

  7. In situ stress observation in oxide films and how tensile stress influences oxygen ion conduction

    NASA Astrophysics Data System (ADS)

    Fluri, Aline; Pergolesi, Daniele; Roddatis, Vladimir; Wokaun, Alexander; Lippert, Thomas

    2016-02-01

    Many properties of materials can be changed by varying the interatomic distances in the crystal lattice by applying stress. Ideal model systems for investigations are heteroepitaxial thin films where lattice distortions can be induced by the crystallographic mismatch with the substrate. Here we describe an in situ simultaneous diagnostic of growth mode and stress during pulsed laser deposition of oxide thin films. The stress state and evolution up to the relaxation onset are monitored during the growth of oxygen ion conducting Ce0.85Sm0.15O2-δ thin films via optical wafer curvature measurements. Increasing tensile stress lowers the activation energy for charge transport and a thorough characterization of stress and morphology allows quantifying this effect using samples with the conductive properties of single crystals. The combined in situ application of optical deflectometry and electron diffraction provides an invaluable tool for strain engineering in Materials Science to fabricate novel devices with intriguing functionalities.

  8. Heavy Ion Formation in Titan's Ionosphere: Magnetospheric Introduction of Free Oxygen and a Source of Titan's Aerosols?

    NASA Technical Reports Server (NTRS)

    Sittler, E. C., Jr.; Ali, A.; Cooper, J. F.; Hartle, R. E.; Johnson, R. E.; Coates, A. J.; Young, D. T.

    2009-01-01

    Discovery by Cassini's plasma instrument of heavy positive and negative ions within Titan's upper atmosphere and ionosphere has advanced our understanding of ion neutral chemistry within Titan's upper atmosphere, primarily composed of molecular nitrogen, with approx.2.5% methane. The external energy flux transforms Titan's upper atmosphere and ionosphere into a medium rich in complex hydrocarbons, nitriles and haze particles extending from the surface to 1200 km altitudes. The energy sources are solar UV, solar X-rays, Saturn's magnetospheric ions and electrons, solar wind and shocked magnetosheath ions and electrons, galactic cosmic rays (CCR) and the ablation of incident meteoritic dust from Enceladus' E-ring and interplanetary medium. Here it is proposed that the heavy atmospheric ions detected in situ by Cassini for heights >950 km, are the likely seed particles for aerosols detected by the Huygens probe for altitudes <100km. These seed particles may be in the form of polycyclic aromatic hydrocarbons (PAH) containing both carbon and hydrogen atoms CnHx. There could also be hollow shells of carbon atoms, such as C60, called fullerenes which contain no hydrogen. The fullerenes may compose a significant fraction of the seed particles with PAHs contributing the rest. As shown by Cassini, the upper atmosphere is bombarded by magnetospheric plasma composed of protons, H(2+) and water group ions. The latter provide keV oxygen, hydroxyl and water ions to Titan's upper atmosphere and can become trapped within the fullerene molecules and ions. Pickup keV N(2+), N(+) and CH(4+) can also be implanted inside of fullerenes. Attachment of oxygen ions to PAH molecules is uncertain, but following thermalization O(+) can interact with abundant CH4 contributing to the CO and CO2 observed in Titan's atmosphere. If an exogenic keV O(+) ion is implanted into the haze particles, it could become free oxygen within those aerosols that eventually fall onto Titan's surface. The process

  9. Cancer Therapy by Catechins Involves Redox Cycling of Copper Ions and Generation of Reactive Oxygen Species

    PubMed Central

    Farhan, Mohd; Khan, Husain Yar; Oves, Mohammad; Al-Harrasi, Ahmed; Rehmani, Nida; Arif, Hussain; Hadi, Sheikh Mumtaz; Ahmad, Aamir

    2016-01-01

    Catechins, the dietary phytochemicals present in green tea and other beverages, are considered to be potent inducers of apoptosis and cytotoxicity to cancer cells. While it is believed that the antioxidant properties of catechins and related dietary agents may contribute to lowering the risk of cancer induction by impeding oxidative injury to DNA, these properties cannot account for apoptosis induction and chemotherapeutic observations. Catechin (C), epicatechin (EC), epigallocatechin (EGC) and epigallocatechin-3-gallate (EGCG) are the four major constituents of green tea. In this article, using human peripheral lymphocytes and comet assay, we show that C, EC, EGC and EGCG cause cellular DNA breakage and can alternatively switch to a prooxidant action in the presence of transition metals such as copper. The cellular DNA breakage was found to be significantly enhanced in the presence of copper ions. Catechins were found to be effective in providing protection against oxidative stress induced by tertbutylhydroperoxide, as measured by oxidative DNA breakage in lymphocytes. The prooxidant action of catechins involved production of hydroxyl radicals through redox recycling of copper ions. We also determined that catechins, particularly EGCG, inhibit proliferation of breast cancer cell line MDA-MB-231 leading to a prooxidant cell death. Since it is well established that tissue, cellular and serum copper levels are considerably elevated in various malignancies, cancer cells would be more subject to redox cycling between copper ions and catechins to generate reactive oxygen species (ROS) responsible for DNA breakage. Such a copper dependent prooxidant cytotoxic mechanism better explains the anticancer activity and preferential cytotoxicity of dietary phytochemicals against cancer cells. PMID:26861392

  10. Cancer Therapy by Catechins Involves Redox Cycling of Copper Ions and Generation of Reactive Oxygen species.

    PubMed

    Farhan, Mohd; Khan, Husain Yar; Oves, Mohammad; Al-Harrasi, Ahmed; Rehmani, Nida; Arif, Hussain; Hadi, Sheikh Mumtaz; Ahmad, Aamir

    2016-02-04

    Catechins, the dietary phytochemicals present in green tea and other beverages, are considered to be potent inducers of apoptosis and cytotoxicity to cancer cells. While it is believed that the antioxidant properties of catechins and related dietary agents may contribute to lowering the risk of cancer induction by impeding oxidative injury to DNA, these properties cannot account for apoptosis induction and chemotherapeutic observations. Catechin (C), epicatechin (EC), epigallocatechin (EGC) and epigallocatechin-3-gallate (EGCG) are the four major constituents of green tea. In this article, using human peripheral lymphocytes and comet assay, we show that C, EC, EGC and EGCG cause cellular DNA breakage and can alternatively switch to a prooxidant action in the presence of transition metals such as copper. The cellular DNA breakage was found to be significantly enhanced in the presence of copper ions. Catechins were found to be effective in providing protection against oxidative stress induced by tertbutylhydroperoxide, as measured by oxidative DNA breakage in lymphocytes. The prooxidant action of catechins involved production of hydroxyl radicals through redox recycling of copper ions. We also determined that catechins, particularly EGCG, inhibit proliferation of breast cancer cell line MDA-MB-231 leading to a prooxidant cell death. Since it is well established that tissue, cellular and serum copper levels are considerably elevated in various malignancies, cancer cells would be more subject to redox cycling between copper ions and catechins to generate reactive oxygen species (ROS) responsible for DNA breakage. Such a copper dependent prooxidant cytotoxic mechanism better explains the anticancer activity and preferential cytotoxicity of dietary phytochemicals against cancer cells.

  11. Gas-solid interfacial modification of oxygen activity in layered oxide cathodes for lithium-ion batteries.

    PubMed

    Qiu, Bao; Zhang, Minghao; Wu, Lijun; Wang, Jun; Xia, Yonggao; Qian, Danna; Liu, Haodong; Hy, Sunny; Chen, Yan; An, Ke; Zhu, Yimei; Liu, Zhaoping; Meng, Ying Shirley

    2016-01-01

    Lattice oxygen can play an intriguing role in electrochemical processes, not only maintaining structural stability, but also influencing electron and ion transport properties in high-capacity oxide cathode materials for Li-ion batteries. Here, we report the design of a gas-solid interface reaction to achieve delicate control of oxygen activity through uniformly creating oxygen vacancies without affecting structural integrity of Li-rich layered oxides. Theoretical calculations and experimental characterizations demonstrate that oxygen vacancies provide a favourable ionic diffusion environment in the bulk and significantly suppress gas release from the surface. The target material is achievable in delivering a discharge capacity as high as 301 mAh g(-1) with initial Coulombic efficiency of 93.2%. After 100 cycles, a reversible capacity of 300 mAh g(-1) still remains without any obvious decay in voltage. This study sheds light on the comprehensive design and control of oxygen activity in transition-metal-oxide systems for next-generation Li-ion batteries. PMID:27363944

  12. Gas-solid interfacial modification of oxygen activity in layered oxide cathodes for lithium-ion batteries

    DOE PAGES

    Qiu, Bao; Zhang, Minghao; Wu, Lijun; Wang, Jun; Xia, Yonggao; Qian, Danna; Liu, Haodong; Chen, Yan; An, Ke; Zhu, Yimei; et al

    2016-07-01

    Lattice oxygen can play an intriguing role in electrochemical processes, not only maintaining structural stability, but also influencing electron and ion transport properties in high-capacity oxide cathode materials for Li-ion batteries. Here, we report the design of a gas–solid interface reaction to achieve delicate control of oxygen activity through uniformly creating oxygen vacancies without affecting structural integrity of Li-rich layered oxides. Theoretical calculations and experimental characterizations demonstrate that oxygen vacancies provide a favourable ionic diffusion environment in the bulk and significantly suppress gas release from the surface. The target material is achievable in delivering a discharge capacity as high asmore » 301 mAh g–1 with initial Coulombic efficiency of 93.2%. After 100 cycles, a reversible capacity of 300 mAh g–1 still remains without any obvious decay in voltage. Lastly, this study sheds light on the comprehensive design and control of oxygen activity in transition-metal-oxide systems for next-generation Li-ion batteries.« less

  13. Gas-solid interfacial modification of oxygen activity in layered oxide cathodes for lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Qiu, Bao; Zhang, Minghao; Wu, Lijun; Wang, Jun; Xia, Yonggao; Qian, Danna; Liu, Haodong; Hy, Sunny; Chen, Yan; An, Ke; Zhu, Yimei; Liu, Zhaoping; Meng, Ying Shirley

    2016-07-01

    Lattice oxygen can play an intriguing role in electrochemical processes, not only maintaining structural stability, but also influencing electron and ion transport properties in high-capacity oxide cathode materials for Li-ion batteries. Here, we report the design of a gas-solid interface reaction to achieve delicate control of oxygen activity through uniformly creating oxygen vacancies without affecting structural integrity of Li-rich layered oxides. Theoretical calculations and experimental characterizations demonstrate that oxygen vacancies provide a favourable ionic diffusion environment in the bulk and significantly suppress gas release from the surface. The target material is achievable in delivering a discharge capacity as high as 301 mAh g-1 with initial Coulombic efficiency of 93.2%. After 100 cycles, a reversible capacity of 300 mAh g-1 still remains without any obvious decay in voltage. This study sheds light on the comprehensive design and control of oxygen activity in transition-metal-oxide systems for next-generation Li-ion batteries.

  14. Gas-solid interfacial modification of oxygen activity in layered oxide cathodes for lithium-ion batteries.

    PubMed

    Qiu, Bao; Zhang, Minghao; Wu, Lijun; Wang, Jun; Xia, Yonggao; Qian, Danna; Liu, Haodong; Hy, Sunny; Chen, Yan; An, Ke; Zhu, Yimei; Liu, Zhaoping; Meng, Ying Shirley

    2016-01-01

    Lattice oxygen can play an intriguing role in electrochemical processes, not only maintaining structural stability, but also influencing electron and ion transport properties in high-capacity oxide cathode materials for Li-ion batteries. Here, we report the design of a gas-solid interface reaction to achieve delicate control of oxygen activity through uniformly creating oxygen vacancies without affecting structural integrity of Li-rich layered oxides. Theoretical calculations and experimental characterizations demonstrate that oxygen vacancies provide a favourable ionic diffusion environment in the bulk and significantly suppress gas release from the surface. The target material is achievable in delivering a discharge capacity as high as 301 mAh g(-1) with initial Coulombic efficiency of 93.2%. After 100 cycles, a reversible capacity of 300 mAh g(-1) still remains without any obvious decay in voltage. This study sheds light on the comprehensive design and control of oxygen activity in transition-metal-oxide systems for next-generation Li-ion batteries.

  15. Gas–solid interfacial modification of oxygen activity in layered oxide cathodes for lithium-ion batteries

    PubMed Central

    Qiu, Bao; Zhang, Minghao; Wu, Lijun; Wang, Jun; Xia, Yonggao; Qian, Danna; Liu, Haodong; Hy, Sunny; Chen, Yan; An, Ke; Zhu, Yimei; Liu, Zhaoping; Meng, Ying Shirley

    2016-01-01

    Lattice oxygen can play an intriguing role in electrochemical processes, not only maintaining structural stability, but also influencing electron and ion transport properties in high-capacity oxide cathode materials for Li-ion batteries. Here, we report the design of a gas–solid interface reaction to achieve delicate control of oxygen activity through uniformly creating oxygen vacancies without affecting structural integrity of Li-rich layered oxides. Theoretical calculations and experimental characterizations demonstrate that oxygen vacancies provide a favourable ionic diffusion environment in the bulk and significantly suppress gas release from the surface. The target material is achievable in delivering a discharge capacity as high as 301 mAh g−1 with initial Coulombic efficiency of 93.2%. After 100 cycles, a reversible capacity of 300 mAh g−1 still remains without any obvious decay in voltage. This study sheds light on the comprehensive design and control of oxygen activity in transition-metal-oxide systems for next-generation Li-ion batteries. PMID:27363944

  16. Bond-length distributions for ions bonded to oxygen: alkali and alkaline-earth metals

    PubMed Central

    Gagné, Olivier Charles; Hawthorne, Frank Christopher

    2016-01-01

    Bond-length distributions have been examined for 55 configurations of alkali-metal ions and 29 configurations of alkaline-earth-metal ions bonded to oxygen, for 4859 coordination polyhedra and 38 594 bond distances (alkali metals), and for 3038 coordination polyhedra and 24 487 bond distances (alkaline-earth metals). Bond lengths generally show a positively skewed Gaussian distribution that originates from the variation in Born repulsion and Coulomb attraction as a function of interatomic distance. The skewness and kurtosis of these distributions generally decrease with increasing coordination number of the central cation, a result of decreasing Born repulsion with increasing coordination number. We confirm the following minimum coordination numbers: [3]Li+, [3]Na+, [4]K+, [4]Rb+, [6]Cs+, [3]Be2+, [4]Mg2+, [6]Ca2+, [6]Sr2+ and [6]Ba2+, but note that some reported examples are the result of extensive dynamic and/or positional short-range disorder and are not ordered arrangements. Some distributions of bond lengths are distinctly multi-modal. This is commonly due to the occurrence of large numbers of structure refinements of a particular structure type in which a particular cation is always present, leading to an over-representation of a specific range of bond lengths. Outliers in the distributions of mean bond lengths are often associated with anomalous values of atomic displacement of the constituent cations and/or anions. For a sample of [6]Na+, the ratio U eq(Na)/U eq(bonded anions) is partially correlated with 〈[6]Na+—O2−〉 (R 2 = 0.57), suggesting that the mean bond length is correlated with vibrational/displacement characteristics of the constituent ions for a fixed coordination number. Mean bond lengths also show a weak correlation with bond-length distortion from the mean value in general, although some coordination numbers show the widest variation in mean bond length for zero distortion, e.g. Li+ in [4]- and [6]-coordination, Na+ in [4]- and [6

  17. Bond-length distributions for ions bonded to oxygen: alkali and alkaline-earth metals.

    PubMed

    Gagné, Olivier Charles; Hawthorne, Frank Christopher

    2016-08-01

    Bond-length distributions have been examined for 55 configurations of alkali-metal ions and 29 configurations of alkaline-earth-metal ions bonded to oxygen, for 4859 coordination polyhedra and 38 594 bond distances (alkali metals), and for 3038 coordination polyhedra and 24 487 bond distances (alkaline-earth metals). Bond lengths generally show a positively skewed Gaussian distribution that originates from the variation in Born repulsion and Coulomb attraction as a function of interatomic distance. The skewness and kurtosis of these distributions generally decrease with increasing coordination number of the central cation, a result of decreasing Born repulsion with increasing coordination number. We confirm the following minimum coordination numbers: ([3])Li(+), ([3])Na(+), ([4])K(+), ([4])Rb(+), ([6])Cs(+), ([3])Be(2+), ([4])Mg(2+), ([6])Ca(2+), ([6])Sr(2+) and ([6])Ba(2+), but note that some reported examples are the result of extensive dynamic and/or positional short-range disorder and are not ordered arrangements. Some distributions of bond lengths are distinctly multi-modal. This is commonly due to the occurrence of large numbers of structure refinements of a particular structure type in which a particular cation is always present, leading to an over-representation of a specific range of bond lengths. Outliers in the distributions of mean bond lengths are often associated with anomalous values of atomic displacement of the constituent cations and/or anions. For a sample of ([6])Na(+), the ratio Ueq(Na)/Ueq(bonded anions) is partially correlated with 〈([6])Na(+)-O(2-)〉 (R(2) = 0.57), suggesting that the mean bond length is correlated with vibrational/displacement characteristics of the constituent ions for a fixed coordination number. Mean bond lengths also show a weak correlation with bond-length distortion from the mean value in general, although some coordination numbers show the widest variation in mean bond length for zero distortion, e.g. Li(+) in

  18. Bond-length distributions for ions bonded to oxygen: alkali and alkaline-earth metals.

    PubMed

    Gagné, Olivier Charles; Hawthorne, Frank Christopher

    2016-08-01

    Bond-length distributions have been examined for 55 configurations of alkali-metal ions and 29 configurations of alkaline-earth-metal ions bonded to oxygen, for 4859 coordination polyhedra and 38 594 bond distances (alkali metals), and for 3038 coordination polyhedra and 24 487 bond distances (alkaline-earth metals). Bond lengths generally show a positively skewed Gaussian distribution that originates from the variation in Born repulsion and Coulomb attraction as a function of interatomic distance. The skewness and kurtosis of these distributions generally decrease with increasing coordination number of the central cation, a result of decreasing Born repulsion with increasing coordination number. We confirm the following minimum coordination numbers: ([3])Li(+), ([3])Na(+), ([4])K(+), ([4])Rb(+), ([6])Cs(+), ([3])Be(2+), ([4])Mg(2+), ([6])Ca(2+), ([6])Sr(2+) and ([6])Ba(2+), but note that some reported examples are the result of extensive dynamic and/or positional short-range disorder and are not ordered arrangements. Some distributions of bond lengths are distinctly multi-modal. This is commonly due to the occurrence of large numbers of structure refinements of a particular structure type in which a particular cation is always present, leading to an over-representation of a specific range of bond lengths. Outliers in the distributions of mean bond lengths are often associated with anomalous values of atomic displacement of the constituent cations and/or anions. For a sample of ([6])Na(+), the ratio Ueq(Na)/Ueq(bonded anions) is partially correlated with 〈([6])Na(+)-O(2-)〉 (R(2) = 0.57), suggesting that the mean bond length is correlated with vibrational/displacement characteristics of the constituent ions for a fixed coordination number. Mean bond lengths also show a weak correlation with bond-length distortion from the mean value in general, although some coordination numbers show the widest variation in mean bond length for zero distortion, e.g. Li(+) in

  19. Comprehensive derivation of bond-valence parameters for ion pairs involving oxygen

    PubMed Central

    Gagné, Olivier Charles; Hawthorne, Frank Christopher

    2015-01-01

    Published two-body bond-valence parameters for cation–oxygen bonds have been evaluated via the root mean-square deviation (RMSD) from the valence-sum rule for 128 cations, using 180 194 filtered bond lengths from 31 489 coordination polyhedra. Values of the RMSD range from 0.033–2.451 v.u. (1.1–40.9% per unit of charge) with a weighted mean of 0.174 v.u. (7.34% per unit of charge). The set of best published parameters has been determined for 128 ions and used as a benchmark for the determination of new bond-valence parameters in this paper. Two common methods for the derivation of bond-valence parameters have been evaluated: (1) fixing B and solving for R o; (2) the graphical method. On a subset of 90 ions observed in more than one coordination, fixing B at 0.37 Å leads to a mean weighted-RMSD of 0.139 v.u. (6.7% per unit of charge), while graphical derivation gives 0.161 v.u. (8.0% per unit of charge). The advantages and disadvantages of these (and other) methods of derivation have been considered, leading to the conclusion that current methods of derivation of bond-valence parameters are not satisfactory. A new method of derivation is introduced, the GRG (generalized reduced gradient) method, which leads to a mean weighted-RMSD of 0.128 v.u. (6.1% per unit of charge) over the same sample of 90 multiple-coordination ions. The evaluation of 19 two-parameter equations and 7 three-parameter equations to model the bond-valence–bond-length relation indicates that: (1) many equations can adequately describe the relation; (2) a plateau has been reached in the fit for two-parameter equations; (3) the equation of Brown & Altermatt (1985 ▸) is sufficiently good that use of any of the other equations tested is not warranted. Improved bond-valence parameters have been derived for 135 ions for the equation of Brown & Altermatt (1985 ▸) in terms of both the cation and anion bond-valence sums using the GRG method and our complete data set. PMID

  20. Determination of adsorbable organic fluorine from aqueous environmental samples by adsorption to polystyrene-divinylbenzene based activated carbon and combustion ion chromatography.

    PubMed

    Wagner, Andrea; Raue, Brigitte; Brauch, Heinz-Jürgen; Worch, Eckhard; Lange, Frank T

    2013-06-21

    A new method for the determination of trace levels of adsorbable organic fluorine (AOF) in water is presented. Even if the individual contributing target compounds are widely unknown, this surrogate parameter is suited to identify typical organofluorine contaminations, such as with polyfluorinated chemicals (PFCs), and represents a lower boundary of the organofluorine concentration in water bodies. It consists of the adsorption of organofluorine chemicals on a commercially available synthetic polystyrene-divinylbenzene based activated carbon (AC) followed by analysis of the loaded AC by hydropyrolysis combustion ion chromatography (CIC). Inorganic fluorine is displaced by excess nitrate during the extraction step and by washing the loaded activated carbon with an acidic sodium nitrate solution. Due to its high purity the synthetic AC had a very low and reproducible fluorine blank (0.3 μg/g) compared to natural ACs (up to approximately 9 μg/g). Using this AC, fluoride and the internal standard phosphate could be detected free of chromatographic interferences. With a sample volume of 100 mL and 2× 100 mg of AC packed into two extraction columns combined in series, a limit of quantification (LOQ), derived according to the German standard method DIN 32645, of 0.3 μg/L was achieved. The recoveries of six model PFCs were determined from tap water and a municipal wastewater treatment plant (WWTP) effluent. Except for the extremely polar perfluoroacetic acid (recovery of approximately 10%) the model substances showed fairly good (50% for perfluorobutanoic acid (PFBA)) to very good fluorine recoveries (100±20% for perfluorooctanoic acid (PFOA), perfluorobutanesulfonate (PFBS), 6:2 fluorotelomersulfonate (6:2 FTS)), both from tap water and wastewater matrix. This new analytical protocol was exemplarily applied to several surface water and groundwater samples. The obtained AOF values were compared to the fluorine content of 19 target PFCs analyzed by high performance

  1. The kinetics of the oxidation of pyrite by ferric ions and dissolved oxygen: An electrochemical study

    SciTech Connect

    Holmes, P.R.; Crundwell, F.K.

    2000-01-01

    The dissolution of pyrite is important in the geochemical cycling of iron and sulphur, in the formation of acid mine drainage, and in the extraction of metals by bacterial leaching. Many researchers have studied the kinetics of dissolution, and the rate of dissolution has often been found to be half-order in ferric ions or oxygen. Previous work has not adequately explained the kinetics of dissolution of pyrite. The dissolution of pyrite is an oxidation-reduction reaction. The kinetics of the oxidation and reduction half-reactions was studied independently using electrochemical techniques of voltammetry. The kinetics of the overall reaction was studied by the electrochemical technique of potentiometry, which consisted of measuring the mixed potential of a sample of corroding pyrite in solutions of different compositions. The kinetics of the half reactions are related to the kinetics of the overall dissolution reaction by the condition that there is no accumulation of charge. This principle is used to derive expressions for the mixed potential and the rate of dissolution, which successfully describe the mixed potential measurements and the kinetics of dissolution reported in the literature. It is shown that the observations of half-order kinetics and that the oxygen in the sulphate product arises from water are both a direct consequence of the electrochemical mechanism. Thus it is concluded that the electrochemical reaction steps occurring at the mineral-solution interface control the rate of dissolution. Raman spectroscopy was used to analyze reaction products formed on the pyrite surface. The results indicated that small amounts of polysulphides form on the surface of the pyrite. However, it was also found that the mixed (corrosion) potential does not change over a 14-day leaching period. This indicates that even though polysulphide material is present on the surface, it does not influence the rate of the reactions occurring at the surface. Measurement of the

  2. Copper ions stimulate the proliferation of hepatic stellate cells via oxygen stress in vitro.

    PubMed

    Xu, San-qing; Zhu, Hui-yun; Lin, Jian-guo; Su, Tang-feng; Liu, Yan; Luo, Xiao-ping

    2013-02-01

    This study examined the effect of copper ions on the proliferation of hepatic stellate cells (HSCs) and the role of oxidative stress in this process in order to gain insight into the mechanism of hepatic fibrosis in Wilson's disease. LX-2 cells, a cell line of human HSCs, were cultured in vitro and treated with different agents including copper sulfate, N-acetyl cysteine (NAC) and buthionine sulfoximine (BSO) for different time. The proliferation of LX-2 cells was measured by non-radioactive cell proliferation assay. Real-time PCR and Western blotting were used to detect the mRNA and protein expression of platelet-derived growth factor receptor β subunit (PDGFβR), ELISA to determine the level of glutathione (GSH) and oxidized glutathione (GSSG), dichlorofluorescein assay to measure the level of reactive oxygen species (ROS), and lipid hydroperoxide assay to quantify the level of lipid peroxide (LPO). The results showed that copper sulfate over a certain concentration range could promote the proliferation of LX-2 cells in a time- and dose-dependent manner. The effect was most manifest when LX-2 cells were treated with copper sulfate at a concentration of 100 μmol/L for 24 h. Additionally, copper sulfate could dose-dependently increase the levels of ROS and LPO, and decrease the ratio of GSH/GSSG in LX-2 cells. The copper-induced increase in mRNA and protein expression of PDGFβR was significantly inhibited in LX-2 cells pre-treated with NAC, a precursor of GSH, and this phenomenon could be reversed by the intervention of BSO, an inhibitor of NAC. It was concluded that copper ions may directly stimulate the proliferation of HSCs via oxidative stress. Anti-oxidative stress therapies may help suppress the copper-induced activation and proliferation of HSCs.

  3. Oxygen isotope analysis of fossil organic matter by secondary ion mass spectrometry

    NASA Astrophysics Data System (ADS)

    Tartèse, Romain; Chaussidon, Marc; Gurenko, Andrey; Delarue, Frédéric; Robert, François

    2016-06-01

    We have developed an analytical procedure for the measurement of oxygen isotope composition of fossil organic matter by secondary ion mass spectrometry (SIMS) at the sub-per mill level, with a spatial resolution of 20-30 μm. The oxygen isotope composition of coal and kerogen samples determined by SIMS are on average consistent with the bulk oxygen isotope compositions determined by temperature conversion elemental analysis - isotope ratio mass spectrometry (TC/EA-IRMS), but display large spreads of δ18O of ∼5-10‰, attributed to mixing of remnants of organic compounds with distinct δ18O signatures. Most of the δ18O values obtained on two kerogen residues extracted from the Eocene Clarno and Early Devonian Rhynie continental chert samples and on two immature coal samples range between ∼10‰ and ∼25‰. Based on the average δ18O values of these samples, and on the O isotope composition of water processed by plants that now constitute the Eocene Clarno kerogen, we estimated δ18Owater values ranging between around -11‰ and -1‰, which overall correspond well within the range of O isotope compositions for present-day continental waters. SIMS analyses of cyanobacteria-derived organic matter from the Silurian Zdanow chert sample yielded δ18O values in the range 12-20‰. Based on the O isotope composition measured on recent cyanobacteria from the hypersaline Lake Natron (Tanzania), and on the O isotope composition of the lake waters in which they lived, we propose that δ18O values of cyanobacteria remnants are enriched by about ∼18 ± 2‰ to 22 ± 2‰ relative to coeval waters. This relationship suggests that deep ocean waters in which the Zdanow cyanobacteria lived during Early Silurian times were characterised by δ18O values of around -5 ± 4‰. This study, establishing the feasibility of micro-analysis of Phanerozoic fossil organic matter samples by SIMS, opens the way for future investigations of kerogens preserved in Archean cherts and of the

  4. NIRS-Derived Tissue Oxygen Saturation and Hydrogen Ion Concentration Following Bed Rest

    NASA Technical Reports Server (NTRS)

    Lee, S. M. C.; Everett, M. E.; Crowell, J. B.; Westby, C. M.; Soller, B. R.

    2010-01-01

    Long-term bed rest (BR), a model of spaceflight, results in a decrease in aerobic capacity and altered submaximal exercise responses. The strongest BR-induced effects on exercise appear to be centrally-mediated, but longer BR durations may result in peripheral adaptations (e.g., decreased mitochondrial and capillary density) which are likely to influence exercise responses. PURPOSE: To measure tissue oxygen saturation (SO2) and hydrogen ion concentration ([H+]) in the vastus lateralis (VL) using near infrared spectroscopy (NIRS) during cycle ergometry before and after . 30 d of BR. METHODS: Eight subjects performed a graded exercise test on a cycle ergometer to volitional fatigue 7 d before (pre-BR) and at the end or 1 day after BR (post-BR). NIRS spectra were collected from a sensor adhered to the skin overlying the VL. Oxygen consumption (VO2) was measured by open circuit spirometry. Blood volume (BV) was measured before and after BR using the carbon monoxide rebreathing technique. Changes in pre- and post-BR SO2 and [H+] data were compared using mixed model analyses. BV and peak exercise data were compared using paired t-tests. RESULTS: BV (pre-BR: 4.3+/-0.3, post-BR: 3.7+/-0.2 L, mean+/-SE, p=.01) and peak VO2 (pre-BR: 1.98+/-0.24, post-BR: 1.48 +/-0.21 L/min, p<.01) were reduced after BR. As expected, SO2 decreased with exercise before and after BR. However, SO2 was lower post compared with pre-BR throughout exercise, including at peak exercise (pre-BR: 50+/-3, post-BR: 43+/-4%, p=.01). After BR, [H+] was higher at the start of exercise and did not increase at the same rate as pre-BR. Peak [H+] was not different from pre to post-BR (pre-BR: 36+/-2; post-BR: 38+/-2 nmol/L). CONCLUSIONS: Lower SO2 during exercise suggests that oxygen extraction in the VL is higher after BR, perhaps due to lower circulating blood volume. The higher [H+] after BR suggests a greater reliance upon glycolysis during submaximal exercise, although [H+] at peak exercise was unchanged

  5. Oxygen chemisorption on V/sub 2/O/sub 5/: isotherms and isobars of adsorption

    SciTech Connect

    Rey, L.; Gambaro, L.A.; Thomas, H.J.

    1984-06-01

    Experimental results of oxygen adsorption on V/sub 2/O/sub 5/ (isotherms and isobars) are reported. In its normal state V/sub 2/O/sub 5/ is a nonstoichiometric oxide that shows oxygen vacancies with the subsequent formation of V/sup 4 +/ ions. A model is developed for the interaction between oxygen (gaseous, adsorbed, and bulk) and the solid phase (V/sub 2/O/sub 5/). 12 references, 4 figures, 1 table.

  6. From trihydrogen interstellar ion to hydrogen-oxygen reaction networks in terrestrial middle atmosphere

    NASA Astrophysics Data System (ADS)

    Varandas, A. J. C.

    After a brief overview on the generalized Born-Oppenheimer approximation and global modelling of electronic manifolds, we focus on two case histories. In the first, we report an accurate double-sheet potential energy surface1 and ro-vibrational calculations1,2 for the H3+(3A') ion which is of relevance in interstellar and plasma chemistries. In the second, we examine odd-hydrogen systems with up to five oxygen atoms which play a crucial role in the chemistry of the middle atmosphere. The premise will then be that all processes occur adiabatically on the relevant ground state potential energy surface, with the emphasis being on our recent observation that highly vibrationally excited spaecies such as O2(v) and OH (v) can hardly thermalize at such altitudes3, thus offering4 within this situation of local thermodynamic disequilibrium a possible clue for know mesospheric mysteries such as the ``ozone deficit problem'' and ``HOx dilemma''. We conclude with some remarks on continuing challenges and planned work.

  7. Planar and channel waveguides on Na:CBN formed by oxygen ion implantation

    NASA Astrophysics Data System (ADS)

    Guo, Sha-Sha; Zhao, Jin-Hua; Huang, Qing; Liu, Peng; Liu, Tao; Zhang, Lian; Wang, Xue-Lin

    2012-09-01

    We reported the fabrication of the planar and channel waveguides in Na-doped calcium barium niobate (CBN) with multiple-energy oxygen-ion implantation. Multiple-energy implants can broaden the barrier width to reduce light leakage from the waveguide to the substrate through the barrier wall. The guiding modes and the near-field intensity distribution of the light were measured by the prism-coupling method and the end-facing coupling arrangement separately. The refractive index profiles of planar and channel waveguides were both typical "well + barrier" distribution, and we used the finite-difference beam propagation method (FD-BPM) to simulate the light propagation. After annealing at 200 °C for 30 min, the waveguide propagation loss of the planar and channel waveguides could be reduced down to ˜3.7 dB/cm and ˜3.5 dB/cm. The calculated results were in excellent agreement with the measured waveguide modes, indicating the feasibility of designing these devices.

  8. Theoretical and experimental investigation of carnosine and its oxygenated adducts. The reaction with the nickel ion

    NASA Astrophysics Data System (ADS)

    Pavlos, Dimitrios; Petropouleas, Panayiotis; Hatzipanayioti, Despina

    2015-11-01

    DFT theoretical calculations at B3LYP/TZVP or LANL2DZ level of theory, for neutral, zwitterions, protonated and anionic carnosine, were performed. Energies, the structural and spectroscopic parameters were calculated in the gas phase and aqueous medium. Additional H-bonds stabilize the ionized forms of carnosine, creating "nests" into which metal ions or bio-molecules may be sheltered. Based on Fukui functions, the reactivity of the abovementioned forms of carnosine, with 1O2, may lead to oxygenated species. The theoretical spectroscopic parameters have been correlated to our experimental results. The effect of H2O2 and the electrochemistry of aqueous carnosine solutions were examined. Theoretical models containing Ni(II), carnosine and water were constructed. In the isolated mauve solid, formulated [Ni(carn)2(H2O)5], the COOsbnd , Nπ and/or NH2 were bonded. When H2O2 was added, the imidazole NMR signals disappeared. A redox couple clearly indicates one electron process, the electron coming from either the oxidation of imidazole ring or the nickel(II)/Ni(III) couple.

  9. Electrochemistry of mixed oxygen ion and electron conducting electrodes in solid electrolyte cells.

    PubMed

    Chueh, William C; Haile, Sossina M

    2012-01-01

    Mixed ion and electron conductors (MIECs) have garnered increased attention as active components in the electrodes of solid oxide electrolyzers (for electricity to fuel conversion) and especially of solid oxide fuel cells (for fuel to electricity conversion). Although much of the work in the literature is directed toward the understanding of oxygen electroreduction on the surfaces of MIECs, more recent studies also explore the role of these materials in fuel electrooxidation. In both cases, the rich chemical and electronic behaviors of MIECs imply a broad range of possible reaction pathways. We highlight the significant progress that has been made in elucidating these pathways through well-designed experimental and computational studies. At the macroscopic level, patterned electrode studies enable identification of active sites, whereas at the microscopic level, surface-sensitive techniques in combination with atomistic-level simulations are beginning to reveal the nature of the rate-determining step(s) and enable rational design of materials with enhanced activity. PMID:22483265

  10. The spatial distribution of negative oxygen ion densities in a dc reactive magnetron discharge

    NASA Astrophysics Data System (ADS)

    Scribbins, Steven; Bowes, Michael; Bradley, James W.

    2013-01-01

    Using Langmuir probe-assisted eclipse laser photodetachment, the spatial distribution of O- densities in the bulk plasma of magnetron sputter tool has been determined for a range of pressures, 0.79 to 2.40 Pa. The discharge was operated in dc (200 W) with a Ti target and a fixed oxygen-argon pressure ratio of 0.2, in poisoned mode. Measurements show significant O- densities occupying an annulus downstream from the magnetic trap in regions of most positive plasma potential. With increasing pressure the region of high O- density expands and the peak densities increase reaching ˜1.5 × 1016 m-3 at 2.40 Pa, corresponding to an O- to electron density ratio (electronegativity α) of ˜2. Outside the area of dense negative ions, and in regions of the magnetic trap accessible to our probe we measure α < 0.2. The results show that these reactive magnetron plasmas, utilized for oxide film production, to be highly electronegative in regions close to the substrate.

  11. Can oxygen deficient SmFeAsO1 - x be synthesized?: Unintentional incorporation of hydride ion at oxygen vacancy site

    NASA Astrophysics Data System (ADS)

    Muraba, Yoshinori; Iimura, Soshi; Matsuishi, Satoru; Hosono, Hideo

    Hydrogen substitution and introduction of oxygen vacancy are effective electron doping methods for the LnFeAsO. However, their Tc vs e-/Fe diagrams do not entirely overlap each other, while Tc vs lattice dimension relationships are very similar. These contradictions can be understood by assuming that unintentional hydrogen is incorporated into the oxygen vacancy. To examine the preferred electron-dopant species in LnFeAsO and the influence of the atmosphere during synthesis on the formation of LnFeAsO1- x , we try to synthesize the SmFeAsO1- x under three well-controlled atmosphere (H2O, H2 and H2O- and H2-free). Under H2O and H2 atmosphere, hydrogen were incorporated at oxygen sites as the hydride ion and SmFeAsO1- x Hx was formed. On the other hand, when H2O and H2 were removed from synthetic process, nearly stoichiometric SmFeAsO was formed. Furthermore, DFT calculations showed that H-substituted samples are more stable than oxygen deficient samples. These results strongly imply that the reported LnFeAsO1- x was contaminated with unintentional hydrogen and LnFeAsO1- x Hx was misidentified as LnFeAsO1- x .

  12. Is the surface oxygen exchange rate linked to bulk ion diffusivity in mixed conducting Ruddlesden–Popper phases?

    DOE PAGES

    Tomkiewicz, Alex C.; Tamimi, Mazin A.; Huq, Ashfia; McIntosh, Steven

    2015-03-02

    There is a possible link between oxygen surface exchange rate and bulk oxygen anion diffusivity in mixed ionic and electronic conducting oxides; it is a topic of great interest and debate. While a large body of experimental evidence and theoretical analyses support a link, observed differences between bulk and surface composition of these materials are hard to reconcile with this observation. This is further compounded by potential problems with simultaneous measurement of both parameters. Here we utilize separate techniques, in situ neutron diffraction and pulsed isotopic surface exchange, to examine bulk ion mobility and surface oxygen exchange rates of threemore » Ruddlesden-Popper phases, general form An-1A2'BnO3n+1, An-1A2'BnX3n+1; LaSrCo0.5Fe0.5O4-δ (n = 1), La0.3Sr2.7CoFeO7-δ (n = 2) and LaSr3Co1.5Fe1.5O10-δ (n = 3). These measurements are complemented by surface composition determination via high sensitivity-low energy ion scattering. We observe a correlation between bulk ion mobility and surface exchange rate between materials. The surface exchange rates vary by more than one order of magnitude with high anion mobility in the bulk of an oxygen vacancy-rich n = 2 Ruddlesden-Popper material correlating with rapid oxygen exchange. Furthermore this is in contrast with the similar surface exchange rates which we may expect due to similar surface compositions across all three samples. This paper conclude that experimental limitations lead to inherent convolution of surface and bulk rates, and that surface exchange steps are not likely to be rate limiting in oxygen incorporation.« less

  13. Is the surface oxygen exchange rate linked to bulk ion diffusivity in mixed conducting Ruddlesden-Popper phases?

    PubMed

    Tomkiewicz, Alex C; Tamimi, Mazin A; Huq, Ashfia; McIntosh, Steven

    2015-01-01

    The possible link between oxygen surface exchange rate and bulk oxygen anion diffusivity in mixed ionic and electronic conducting oxides is a topic of great interest and debate. While a large body of experimental evidence and theoretical analyses support a link, observed differences between bulk and surface composition of these materials are hard to reconcile with this observation. This is further compounded by potential problems with simultaneous measurement of both parameters. Here we utilize separate techniques, in situ neutron diffraction and pulsed isotopic surface exchange, to examine bulk ion mobility and surface oxygen exchange rates of three Ruddlesden-Popper phases, general form A(n-1)A(2)'B(n)O(3n+1), A(n-1)A(2)'B(n)X(3n+1); LaSrCo(0.5)Fe(0.5)O(4-δ) (n = 1), La(0.3)Sr(2.7)CoFeO(7-δ) (n = 2) and LaSr3Co(1.5)Fe(1.5)O(10-δ) (n = 3). These measurements are complemented by surface composition determination via high sensitivity-low energy ion scattering. We observe a correlation between bulk ion mobility and surface exchange rate between materials. The surface exchange rates vary by more than one order of magnitude with high anion mobility in the bulk of an oxygen vacancy-rich n = 2 Ruddlesden-Popper material correlating with rapid oxygen exchange. This is in contrast with the similar surface exchange rates which we may expect due to similar surface compositions across all three samples. We conclude that experimental limitations lead to inherent convolution of surface and bulk rates, and that surface exchange steps are not likely to be rate limiting in oxygen incorporation.

  14. The dynamics of reductive sorption of oxygen by a granular bed of electron-ion exchangers with different copper dispersities

    NASA Astrophysics Data System (ADS)

    Konev, D. V.; Kravchenko, T. A.; Kalinichev, A. I.; Kipriyanova, E. S.

    2009-05-01

    The behavior of an immobile granular sorbent bed in one-component sorption in a column reactor is described in terms of the kinetic model of redox sorption taking into consideration the dispersity of metal particles, their radial distribution, peculiarities of chemical oxidation, and the relation of the overall rate of the process to the properties of the ion exchange matrix. The mathematical problem is formulated and solved numerically; the solution is analyzed theoretically in relation to the basic parameters of the sorption system. A satisfactory agreement is obtained between the experimental and calculated data on the reductive sorption of molecular oxygen from water on a copper-containing electron-ion exchanger.

  15. Mass spectrometry of positive ions in capacitively coupled low pressure RF discharges in oxygen with water impurities

    NASA Astrophysics Data System (ADS)

    Stefanović, Ilija; Stojanović, Vladimir; Boulmer-Leborgne, Chantal; Lecas, Thomas; Kovacevic, Eva; Berndt, Johannes

    2016-07-01

    A capacitively coupled RF oxygen discharge is studied by means of mass spectroscopy. Mass spectra of neutral and positive species are measured in the mid plane between the electrodes at different distances between plasma and mass-spectrometer orifice. In the case of positive ions, as expected, the largest flux originates from \\text{O}2+ . However, a significant number of impurities are detected, especially for low input powers and larger distances. The most abundant positive ions (besides \\text{O}2+ ) are \\text{N}{{\\text{O}}+}, \\text{NO}2+ , {{\\text{H}}+}≤ft({{\\text{H}}2}\\text{O}\\right) , and {{\\text{H}}+}{{≤ft({{\\text{H}}2}\\text{O}\\right)}2} . In particular, for the case of hydrated hydronium ions {{\\text{H}}+}{{≤ft({{\\text{H}}2}\\text{O}\\right)}n} (n  =  1, 2) a surprisingly large flux (for low pressure plasma conditions) is detected. Another interesting fact concerns the {{\\text{H}}2}{{\\text{O}}+} ions. Despite the relatively high ammount of water impurities {{\\text{H}}2}{{\\text{O}}+} ions are present only in traces. The reaction mechanisms leading to the production of the observed ions, especially the hydrated hydronium ions are discussed.

  16. Frictional behavior and adhesion of Ag and Au films applied to aluminum oxide by oxygen-ion assisted Screen Cage Ion Plating (SCIP)

    NASA Technical Reports Server (NTRS)

    Spalvins, Talivaldis; Sliney, Harold E.

    1994-01-01

    A modified dc-diode ion plating system, by utilizing a metallic screen cage as a cathode, is introduced for coating nonconductors such as ceramics. Screen cage ion plating (SCIP) is used to apply Ag and Au lubricating films on aluminum oxide surfaces. This process has excellent ability to coat around corners to produce three-dimensional coverage of the substrate. A dramatic increase in adhesion is achieved when plating is performed in a reactive 50 percent O2 - 50 percent Ar glow discharge compared to the adhesion when plating is performed in 100 percent Ar. The presence of oxygen ion assistance contributes to the excellent adhesion as measured in a pull-type adhesion tester. The Ag and Au film adhesion is significantly increased (less than 70MPa) and generally exceeds the cohesion of the substrate such that portions of the alumina are pulled out.

  17. Low Doses of Oxygen Ion Irradiation Cause Acute Damage to Hematopoietic Cells in Mice.

    PubMed

    Chang, Jianhui; Luo, Yi; Wang, Yingying; Pathak, Rupak; Sridharan, Vijayalakshmi; Jones, Tamako; Mao, Xiao Wen; Nelson, Gregory; Boerma, Marjan; Hauer-Jensen, Martin; Zhou, Daohong; Shao, Lijian

    2016-01-01

    One of the major health risks to astronauts is radiation on long-duration space missions. Space radiation from sun and galactic cosmic rays consists primarily of 85% protons, 14% helium nuclei and 1% high-energy high-charge (HZE) particles, such as oxygen (16O), carbon, silicon, and iron ions. HZE particles exhibit dense linear tracks of ionization associated with clustered DNA damage and often high relative biological effectiveness (RBE). Therefore, new knowledge of risks from HZE particle exposures must be obtained. In the present study, we investigated the acute effects of low doses of 16O irradiation on the hematopoietic system. Specifically, we exposed C57BL/6J mice to 0.1, 0.25 and 1.0 Gy whole body 16O (600 MeV/n) irradiation and examined the effects on peripheral blood (PB) cells, and bone marrow (BM) hematopoietic stem cells (HSCs) and hematopoietic progenitor cells (HPCs) at two weeks after the exposure. The results showed that the numbers of white blood cells, lymphocytes, monocytes, neutrophils and platelets were significantly decreased in PB after exposure to 1.0 Gy, but not to 0.1 or 0.25 Gy. However, both the frequency and number of HPCs and HSCs were reduced in a radiation dose-dependent manner in comparison to un-irradiated controls. Furthermore, HPCs and HSCs from irradiated mice exhibited a significant reduction in clonogenic function determined by the colony-forming and cobblestone area-forming cell assays. These acute adverse effects of 16O irradiation on HSCs coincided with an increased production of reactive oxygen species (ROS), enhanced cell cycle entry of quiescent HSCs, and increased DNA damage. However, none of the 16O exposures induced apoptosis in HSCs. These data suggest that exposure to low doses of 16O irradiation induces acute BM injury in a dose-dependent manner primarily via increasing ROS production, cell cycling, and DNA damage in HSCs. This finding may aid in developing novel strategies in the protection of the hematopoietic

  18. Low Doses of Oxygen Ion Irradiation Cause Acute Damage to Hematopoietic Cells in Mice

    PubMed Central

    Wang, Yingying; Pathak, Rupak; Sridharan, Vijayalakshmi; Jones, Tamako; Mao, Xiao Wen; Nelson, Gregory; Boerma, Marjan; Hauer-Jensen, Martin; Zhou, Daohong; Shao, Lijian

    2016-01-01

    One of the major health risks to astronauts is radiation on long-duration space missions. Space radiation from sun and galactic cosmic rays consists primarily of 85% protons, 14% helium nuclei and 1% high-energy high-charge (HZE) particles, such as oxygen (16O), carbon, silicon, and iron ions. HZE particles exhibit dense linear tracks of ionization associated with clustered DNA damage and often high relative biological effectiveness (RBE). Therefore, new knowledge of risks from HZE particle exposures must be obtained. In the present study, we investigated the acute effects of low doses of 16O irradiation on the hematopoietic system. Specifically, we exposed C57BL/6J mice to 0.1, 0.25 and 1.0 Gy whole body 16O (600 MeV/n) irradiation and examined the effects on peripheral blood (PB) cells, and bone marrow (BM) hematopoietic stem cells (HSCs) and hematopoietic progenitor cells (HPCs) at two weeks after the exposure. The results showed that the numbers of white blood cells, lymphocytes, monocytes, neutrophils and platelets were significantly decreased in PB after exposure to 1.0 Gy, but not to 0.1 or 0.25 Gy. However, both the frequency and number of HPCs and HSCs were reduced in a radiation dose-dependent manner in comparison to un-irradiated controls. Furthermore, HPCs and HSCs from irradiated mice exhibited a significant reduction in clonogenic function determined by the colony-forming and cobblestone area-forming cell assays. These acute adverse effects of 16O irradiation on HSCs coincided with an increased production of reactive oxygen species (ROS), enhanced cell cycle entry of quiescent HSCs, and increased DNA damage. However, none of the 16O exposures induced apoptosis in HSCs. These data suggest that exposure to low doses of 16O irradiation induces acute BM injury in a dose-dependent manner primarily via increasing ROS production, cell cycling, and DNA damage in HSCs. This finding may aid in developing novel strategies in the protection of the hematopoietic

  19. Low Doses of Oxygen Ion Irradiation Cause Acute Damage to Hematopoietic Cells in Mice.

    PubMed

    Chang, Jianhui; Luo, Yi; Wang, Yingying; Pathak, Rupak; Sridharan, Vijayalakshmi; Jones, Tamako; Mao, Xiao Wen; Nelson, Gregory; Boerma, Marjan; Hauer-Jensen, Martin; Zhou, Daohong; Shao, Lijian

    2016-01-01

    One of the major health risks to astronauts is radiation on long-duration space missions. Space radiation from sun and galactic cosmic rays consists primarily of 85% protons, 14% helium nuclei and 1% high-energy high-charge (HZE) particles, such as oxygen (16O), carbon, silicon, and iron ions. HZE particles exhibit dense linear tracks of ionization associated with clustered DNA damage and often high relative biological effectiveness (RBE). Therefore, new knowledge of risks from HZE particle exposures must be obtained. In the present study, we investigated the acute effects of low doses of 16O irradiation on the hematopoietic system. Specifically, we exposed C57BL/6J mice to 0.1, 0.25 and 1.0 Gy whole body 16O (600 MeV/n) irradiation and examined the effects on peripheral blood (PB) cells, and bone marrow (BM) hematopoietic stem cells (HSCs) and hematopoietic progenitor cells (HPCs) at two weeks after the exposure. The results showed that the numbers of white blood cells, lymphocytes, monocytes, neutrophils and platelets were significantly decreased in PB after exposure to 1.0 Gy, but not to 0.1 or 0.25 Gy. However, both the frequency and number of HPCs and HSCs were reduced in a radiation dose-dependent manner in comparison to un-irradiated controls. Furthermore, HPCs and HSCs from irradiated mice exhibited a significant reduction in clonogenic function determined by the colony-forming and cobblestone area-forming cell assays. These acute adverse effects of 16O irradiation on HSCs coincided with an increased production of reactive oxygen species (ROS), enhanced cell cycle entry of quiescent HSCs, and increased DNA damage. However, none of the 16O exposures induced apoptosis in HSCs. These data suggest that exposure to low doses of 16O irradiation induces acute BM injury in a dose-dependent manner primarily via increasing ROS production, cell cycling, and DNA damage in HSCs. This finding may aid in developing novel strategies in the protection of the hematopoietic

  20. Oxygen surface exchange and diffusion in the new perovskite oxide ion conductor LaGaO{sub 3}

    SciTech Connect

    Ishihara, Tatsumi; Honda, Miho; Takita, Yusaku; Kilner, J.A.

    1997-03-19

    One of the aims of these experiments was to verify that the oxygen ion is the majority carrier in LaGaO{sub 3}-based materials, as they are thought to exhibit p-type conductivity in the high oxygen partial pressure range. Specifically, we have investigated oxygen surface exchange and diffusion in La{sub 0.9}Sr{sub 0.1}Ga{sub 0.8}Mg{sub 0.2}O{sub 3-x} by {sup 18}O isotopic exchange and SIMS at high partial pressures of oxygen (0.1 MPa). In conclusion, these results show that bulk oxygen diffusion in LSGM is very rapid. By a comparison of the oxygen self-diffusivity obtained from tracer and ionic conductivity, the electrical conductivity observed is ionic in the temperature range we have measured. The surface exchange coefficients are anomalous when compared to other perovskite oxides. The activation enthalpy for surface exchange is higher than that for self diffusion coefficient, a finding observed for two other solid oxide electrolytes with the fluorite structure. This behavior is thought to originate in the low electron concentrations found in these electrolyte materials, particularly at the lowest temperatures. 13 refs., 2 figs.

  1. Element- and charge-state-resolved ion energies in the cathodic arc plasma from composite AlCr cathodes in argon, nitrogen and oxygen atmospheres

    PubMed Central

    Franz, Robert; Polcik, Peter; Anders, André

    2015-01-01

    The energy distribution functions of ions in the cathodic arc plasma using composite AlCr cathodes were measured as a function of the background gas pressure in the range 0.5 to 3.5 Pa for different cathode compositions and gas atmospheres. The most abundant aluminium ions were Al+ regardless of the background gas species, whereas Cr2+ ions were dominating in Ar and N2 and Cr+ in O2 atmospheres. The energy distributions of the aluminium and chromium ions typically consisted of a high-energy fraction due to acceleration in the expanding plasma plume from the cathode spot and thermalised ions that were subjected to collisions in the plasma cloud. The fraction of the latter increased with increasing background gas pressure. Atomic nitrogen and oxygen ions showed similar energy distributions as the aluminium and chromium ions, whereas the argon and molecular nitrogen and oxygen ions were formed at greater distance from the cathode spot and thus less subject to accelerating gradients. In addition to the positively charged metal and gas ions, negatively charged oxygen and oxygen-containing ions were observed in O2 atmosphere. The obtained results are intended to provide a comprehensive overview of the ion energies and charge states in the arc plasma of AlCr composite cathodes in different gas atmospheres as such plasmas are frequently used to deposit thin films and coatings. PMID:26120236

  2. Multiple ionization and coupling effects in L-subshell ionization of heavy atoms by oxygen ions

    SciTech Connect

    Pajek, M.; Banas, D.; Semaniak, J.; Braziewicz, J.; Majewska, U.; Chojnacki, S.; Czyzewski, T.; Fijal, I.; Jaskola, M.; Glombik, A.; Kretschmer, W.; Trautmann, D.; Lapicki, G.; Mukoyama, T.

    2003-08-01

    The multiple-ionization and coupling effects in L-shell ionization of atoms by heavy-ion impact have been studied by measuring the L x-ray production cross sections in solid targets of Au, Bi, Th, and U bombarded by oxygen ions in the energy range 6.4-70 MeV. The measured L x-ray spectra were analyzed using the recently proposed method accounting for the multiple-ionization effects, such as x-ray line shifting and broadening, which enables one to obtain the ionization probabilities for outer shells. The L-subshell ionization cross sections have been obtained from measured x-ray production cross sections for resolved L{alpha}{sub 1,2}, L{gamma}{sub 1}, and L{gamma}{sub 2,3} transitions using the L-shell fluorescence and Coster-Kronig yields being substantially modified by the multiple ionization in the M and N shells. In particular, the effect of closing of strong L{sub 1}-L{sub 3}M{sub 4,5} Coster-Kronig transitions in multiple-ionized atoms was evidenced and discussed. The experimental ionization cross sections for the L{sub 1}, L{sub 2}, and L{sub 3} subshells have been compared with the predictions of the semiclassical approximation (SCA) and the ECPSSR theory that includes the corrections for the binding-polarization effect within the perturbed stationary states approximation, the projecticle energy loss, and Coulomb deflection effects as well as the relativistic description of inner-shell electrons. These approaches were further modified to include the L-subshell couplings within the ''coupled-subshell model'' (CSM). Both approaches, when modified for the coupling effects, are in better agreement with the data. Particularly, the predictions of the SCA-CSM calculations reproduce the experimental L-subshell ionization cross section reasonably well. Remaining discrepancies are discussed qualitatively, in terms of further modifications of the L-shell decay rates caused by a change of electronic wave functions in multiple-ionized atoms.

  3. Interactions of Sn2+ dopant ions located on surface sites of anatase-type TiO2 with adsorbed H2S molecules studied using 119Sn Mössbauer spectroscopic probe

    NASA Astrophysics Data System (ADS)

    Fabritchnyi, P. B.; Afanasov, M. I.; Astashkin, R. A.; Wattiaux, A.; Labrugère, C.

    2014-11-01

    Information provided by 119Sn2+ Mössbauer probe ions, located on surface sites of anatase-type TiO2 microcrystals exposed, at room temperature, to a H2S/H2 mixture, has permitted to conclude that the interaction of H2S molecules with the substrate surface leads to the dissociation of a fraction of the absorbate molecules. This gives rise to the formation of elemental sulfur which oxidizes the neighboring Sn2+ ions, the produced Sn4+ ions being found coordinated only by S2- anions. Subsequent exposure to ambient air is shown to result in the oxidation of S2- ions, yielding both S0 and SO42--like species, with concomitant stabilization of Sn4+ ions in coordination polyhedra where they are surrounded by only oxygen anions.

  4. Collisions of carbon and oxygen ions with electrons, H, H/sub 2/ and He: Volume 5

    SciTech Connect

    Phaneuf, R.A.; Janev, R.K.; Pindzola, M.S.

    1987-02-01

    This report provides a handbook for fusion research of recommended cross-section and rate-coefficient data for collisions of carbon and oxygen ions with electrons, hydrogen atoms and molecules, and helium atoms. Published experimental and theoretical data have been collected and evaluated, and recommended data are presented in tabular, graphical, and parametrized form. Processes considered include exciation, ionization, and charge exchange at collision energies appropriate to applications in fusion-energy research.

  5. Antihydrophobic cosolvent effects for alkylation reactions in water solution, particularly oxygen versus carbon alkylations of phenoxide ions.

    PubMed

    Breslow, Ronald; Groves, Kevin; Mayer, M Uljana

    2002-04-10

    Antihydrophobic cosolvents such as ethanol increase the solubility of hydrophobic molecules in water, and they also affect the rates of reactions involving hydrophobic surfaces. In simple reactions of hydrocarbons, such as the Diels-Alder dimerization of 1,3-cyclopentadiene, the rate and solubility data directly reflect the geometry of the transition state, in which some hydrophobic surface becomes hidden. In reactions involving polar groups, such as alkylations of phenoxide ions or S(N)1 ionizations of alkyl halides, cosolvents in water can have other effects as well. However, solvation of hydrophobic surfaces is still important. By the use of structure-reactivity relationships, and comparing the effects of ethanol and DMSO as solvents, it has been possible to sort out these effects. The conclusions are reinforced by an ab initio computer model for hydrophobic solvation. The result is a sensible transition state for phenoxide ion as a nucleophile, using its oxygen n electrons to avoid loss of conjugation. The geometry of alkylation of aniline is very different, involving packing (stacking) of the aniline ring onto the phenyl ring of a benzyl group in the benzylation reaction. The alkylation of phenoxide ions by benzylic chlorides can occur both at the phenoxide oxygen and on ortho and para positions of the ring. Carbon alkylation occurs in water, but not in nonpolar organic solvents, and it is observed only when the phenoxide has at least one methyl substituent ortho, meta, or para. The effects of phenol substituents and of antihydrophobic cosolvents on the rates of the competing alkylation processes indicate that in water the carbon alkylation involves a transition state with hydrophobic packing of the benzyl group onto the phenol ring. The results also support our conclusion that oxygen alkylation uses the n electrons of the phenoxide oxygen as the nucleophile and does not have hydrophobic overlap in the transition state. The mechanisms and explanations for

  6. Mercuric ions inhibit mitogen-activated protein kinase dephosphorylation by inducing reactive oxygen species

    SciTech Connect

    Haase, Hajo; Engelhardt, Gabriela; Hebel, Silke; Rink, Lothar

    2011-01-01

    Mercury intoxication profoundly affects the immune system, in particular, signal transduction of immune cells. However, the mechanism of the interaction of mercury with cellular signaling pathways, such as mitogen activated protein kinases (MAPK), remains elusive. Therefore, the objective of this study is to investigate three potential ways in which Hg{sup 2+} ions could inhibit MAPK dephosphorylation in the human T-cell line Jurkat: (1) by direct binding to phosphatases; (2) by releasing cellular zinc (Zn{sup 2+}); and (3) by inducing reactive oxygen species (ROS). Hg{sup 2+} causes production of ROS, measured by dihydrorhodamine 123, and triggers ROS-mediated Zn{sup 2+} release, detected with FluoZin-3. Yet, phosphatase-inhibition is not mediated by binding of Zn{sup 2+} or Hg{sup 2+}. Rather, phosphatases are inactivated by at least two forms of thiol oxidation; initial inhibition is reversible with reducing agents such as Tris(2-carboxyethyl)phosphine. Prolonged inhibition leads to non-reversible phosphatase oxidation, presumably oxidizing the cysteine thiol to sulfinic- or sulfonic acid. Notably, phosphatases are a particularly sensitive target for Hg{sup 2+}-induced oxidation, because phosphatase activity is inhibited at concentrations of Hg{sup 2+} that have only minor impact on over all thiol oxidation. This phosphatase inhibition results in augmented, ROS-dependent MAPK phosphorylation. MAPK are important regulators of T-cell function, and MAPK-activation by inhibition of phosphatases seems to be one of the molecular mechanisms by which mercury affects the immune system.

  7. Reactions of State-Selected Atomic Oxygen Ions O(+)((4)S, (2)D, (2)P) with Methane.

    PubMed

    Cunha de Miranda, Barbara; Romanzin, Claire; Chefdeville, Simon; Vuitton, Véronique; Žabka, Jan; Polášek, Miroslav; Alcaraz, Christian

    2015-06-11

    An experimental study has been carried out on the reactions of state selected O(+)((4)S, (2)D, (2)P) ions with methane with the aims of characterizing the effects of both the parent ion internal energy and collision energy on the reaction dynamics and determining the fate of oxygen species in complex media, in particular the Titan ionosphere. Absolute cross sections and product velocity distributions have been determined for the reactions of (16)O(+) or (18)O(+) ions with CH4 or CD4 from thermal to 5 eV collision energies by using the guided ion beam (GIB) technique. Dissociative photoionization of O2 with vacuum ultraviolet (VUV) synchrotron radiation delivered by the DESIRS beamline at the SOLEIL storage ring and the threshold photoion photoelectron coincidence (TPEPICO) technique are used for the preparation of purely state-selected O(+)((4)S, (2)D, (2)P) ions. A complete inversion of the product branching ratio between CH4(+) and CH3(+) ions in favor of the latter is observed for excitation of O(+) ions from the (4)S ground state to either the (2)D or the (2)P metastable state. CH4(+) and CH3(+) ions, which are by far the major products for the reaction of ground state and excited states, are strongly backward scattered in the center of mass frame relative to O(+) parent ions. For the reaction of O(+)((4)S), CH3(+) production also rises with increasing collision energy but with much less efficiency than with O(+) excitation. We found that a mechanism of dissociative charge transfer, mediated by an initial charge transfer step, can account very well for all the observations, indicating that CH3(+) production is associated with the formation of H and O atoms (CH3(+) + H + O) rather than with OH formation by an hydride transfer process (CH3(+) + OH). Therefore, as the CH4(+) production by charge transfer is also associated with O atoms, the fate of oxygen species in these reactions is essentially the O production, except for the reaction of O(+)((4)S), which also

  8. Reactions of State-Selected Atomic Oxygen Ions O(+)((4)S, (2)D, (2)P) with Methane.

    PubMed

    Cunha de Miranda, Barbara; Romanzin, Claire; Chefdeville, Simon; Vuitton, Véronique; Žabka, Jan; Polášek, Miroslav; Alcaraz, Christian

    2015-06-11

    An experimental study has been carried out on the reactions of state selected O(+)((4)S, (2)D, (2)P) ions with methane with the aims of characterizing the effects of both the parent ion internal energy and collision energy on the reaction dynamics and determining the fate of oxygen species in complex media, in particular the Titan ionosphere. Absolute cross sections and product velocity distributions have been determined for the reactions of (16)O(+) or (18)O(+) ions with CH4 or CD4 from thermal to 5 eV collision energies by using the guided ion beam (GIB) technique. Dissociative photoionization of O2 with vacuum ultraviolet (VUV) synchrotron radiation delivered by the DESIRS beamline at the SOLEIL storage ring and the threshold photoion photoelectron coincidence (TPEPICO) technique are used for the preparation of purely state-selected O(+)((4)S, (2)D, (2)P) ions. A complete inversion of the product branching ratio between CH4(+) and CH3(+) ions in favor of the latter is observed for excitation of O(+) ions from the (4)S ground state to either the (2)D or the (2)P metastable state. CH4(+) and CH3(+) ions, which are by far the major products for the reaction of ground state and excited states, are strongly backward scattered in the center of mass frame relative to O(+) parent ions. For the reaction of O(+)((4)S), CH3(+) production also rises with increasing collision energy but with much less efficiency than with O(+) excitation. We found that a mechanism of dissociative charge transfer, mediated by an initial charge transfer step, can account very well for all the observations, indicating that CH3(+) production is associated with the formation of H and O atoms (CH3(+) + H + O) rather than with OH formation by an hydride transfer process (CH3(+) + OH). Therefore, as the CH4(+) production by charge transfer is also associated with O atoms, the fate of oxygen species in these reactions is essentially the O production, except for the reaction of O(+)((4)S), which also

  9. Adsorption of o-cresol and benzoic acid in an adsorber packed with an ion-exchange resin: A comparative study of diffusional models

    SciTech Connect

    Run-Tun Huang; Teh-Liang Chen; Hung-Shan Weng

    1994-10-01

    Both solid- and pore-diffusion models were employed to simulate the adsorption of o-cresol and benzoic acid in a fixed-bed adsorber packed with an anion-exchange resin. The equilibrium adsorption data were modeled by a Langmuir isotherm. When the shape of the adsorption isotherm was approximately linear (as in the case of o-cresol), both models agreed well with the experimental break-through data, and they could be effectively applied to predict the breakthrough curve of longer columns. For a favorable adsorption isotherm (say, benzoic acid), however, better results were obtained by using the solid-diffusion model. In addition to the shape of the adsorption isotherm, several factors, such as the type of adsorbent, modeling of equilibrium data, computation efficiency, and concentration dependence of the intraparticle diffusivity, should also be taken into account for selecting a suitable diffusion model.

  10. Nano sponge Mn₂O ₃ as a new adsorbent for the preconcentration of Pd(II) and Rh(III) ions in sea water, wastewater, rock, street sediment and catalytic converter samples prior to FAAS determinations.

    PubMed

    Yavuz, Emre; Tokalıoğlu, Serife; Sahan, Halil; Patat, Saban

    2014-10-01

    In this study, a nano sponge Mn2O3 adsorbent was synthesized and was used for the first time. Various parameters affecting the recovery values of Pd(II) and Rh(III) were examined. The tolerance limits (≥ 90 %) for both Pd(II) and Rh(III) ions were found to be 75,000 mg L(-1) Na(I), 75,000 mg L(-1) K(I), 50,000 mg L(-1) Mg(II) and 50,000 mg L(-1) Ca(II). A 30s contact time was enough for both adsorption and elution. A preconcentration factor of 100 was obtained by using 100mg of the nano sponge Mn2O3. The reusability of the adsorbent was 120 times. Adsorption capacities for Pd(II) and Rh(III) were found to be 42 and 6.2 mg g(-1), respectively. The detection limits were 1.0 µg L(-1) for Pd(II) and 0.37 µg L(-1) for Rh(III) and the relative standard deviations (RSD, %) were found to be ≤ 2.5%. The method was validated by analyzing the standard reference material, SRM 2556 (Used Auto Catalyst Pellets) and spiked real samples. The optimized method was applied for the preconcentration of Pd(II) and Rh(III) ions in water (sea water and wastewater), rock, street sediment and catalytic converter samples.

  11. [The genotoxic action of uranyl ions on DNA in vitro caused by the generation of reactive oxygen species].

    PubMed

    Smirnova, V S; Gudkov, S V; Shtarkman, I N; Chernikov, A V; Bruskov, V I

    2005-01-01

    8-Oxoguanine (8-OG) is an important biomarker of oxidative DNA damage induced by reactive oxygen species (ROS). By using ELISA with monoclonal antibodies against 8-OG, the formation of 8-OG in DNA by the action of uranyl ions, gamma-irradiation, and heating at 37 degrees C and their combined action was investigated in view of environmental pollution by uranium oxides as a result of the use of armor piercing shells with depleted uranium. The content of 8-OG in DNA induced by the action of gamma-irradiation, 5 microM uranyl ions and heating changes with time in a complicated manner. These results suggest that, by the action of uranyl ions, an additional generation of ROS occurs, which leads both to the formation of 8-OG in DNA and its further oxidation. Uranyl ions at a conceptration of 5 microM increase the thermal deamination of cytosine in DNA several times but do not influence DNA thermal depurination. It is shown that uranyl ions essentially increase the production of hydrogen peroxide and hydroxyl radicals by the action of heat on water. The results indicate a high chemical genotoxicity of uranyl ions and their enhancing effect on DNA base damage by the action of heat and gamma-irradiation.

  12. Structural features and enhanced high-temperature oxygen ion transport in SrFe{sub 1-x}Ta{sub x}O{sub 3-{delta}}

    SciTech Connect

    Markov, Alexey A.; Shalaeva, Elizaveta V.; Tyutyunnik, Alexander P.; Kuchin, Vasily V.; Patrakeev, Mikhail V.; Leonidov, Ilya A.; Kozhevnikov, Victor L.

    2013-01-15

    Structural features, oxygen non-stoichiometry and transport properties are studied in the oxide series SrFe{sub 1-x}Ta{sub x}O{sub 3-{delta}}, where x=0.2, 0.3 and 0.4. X-ray diffraction and electron microscopy data evidence formation of the inhomogeneous materials at x=0.3 and 0.4, which include phase constituents with a cubic perovskite and a double perovskite structure types. The composition, the amount and the typical grain size of the phase inhomogeneities are shown to depend both on doping and oxygen content. The increased oxygen-ion conductivity is observed in oxygen depleted materials, which is explained by the increase in the amount of cubic perovskite-like phase and development of interfacial pathways favorable for enhanced oxygen ion transport. - Graphical abstract: The structural studies, oxygen content and conductivity measurements suggest that oxygen depletion from the double perovskite phase constituent of SrFe{sub 1-x}Ta{sub x}O{sub 3-{delta}} for x>0.2 is accompanied by formation of pathways for fast ion transport. Black-Small-Square Highlights: Black-Right-Pointing-Pointer The double perovskite type regions are shown to exist in SrFe{sub 1-x}Ta{sub x}O{sub 3-{delta}}. Black-Right-Pointing-Pointer The oxygen depletion is accompanied with phase separation. Black-Right-Pointing-Pointer The phase separation favors formation of pathways for enhanced oxygen ion transport.

  13. Negative Oxygen Ions Production by Superamphiphobic and Antibacterial TiO2/Cu2O Composite Film Anchored on Wooden Substrates.

    PubMed

    Gao, Likun; Qiu, Zhe; Gan, Wentao; Zhan, Xianxu; Li, Jian; Qiang, Tiangang

    2016-05-27

    According to statistics, early in the 20th century, the proportion of positive and negative air ions on the earth is 1 : 1.2. However, after more than one century, the equilibrium state of the proportion had an obvious change, which the proportion of positive and negative air ions became 1.2 : 1, leading to a surrounding of positive air ions in human living environment. Therefore, it is urgent to adopt effective methods to improve the proportion of negative oxygen ions, which are known as "air vitamin". In this study, negative oxygen ions production by the TiO2/Cu2O-treated wood under UV irradiation was first reported. Anatase TiO2 particles with Cu2O particles were doped on wooden substrates through a two-step method and further modification is employed to create remarkable superamphiphobic surface. The effect of Cu2O particles dopant on the negative oxygen ions production of the TiO2-treated wood was investigated. The results showed that the production of negative oxygen ions was drastically improved by doping with Cu2O particles under UV irradiation. The wood modified with TiO2/Cu2O composite film after hydrophobization is imparted with superamphiphobicity, antibacterial actions against Escherichia coli, and negative oxygen ions production under UV irradiation.

  14. Negative Oxygen Ions Production by Superamphiphobic and Antibacterial TiO2/Cu2O Composite Film Anchored on Wooden Substrates

    PubMed Central

    Gao, Likun; Qiu, Zhe; Gan, Wentao; Zhan, Xianxu; Li, Jian; Qiang, Tiangang

    2016-01-01

    According to statistics, early in the 20th century, the proportion of positive and negative air ions on the earth is 1 : 1.2. However, after more than one century, the equilibrium state of the proportion had an obvious change, which the proportion of positive and negative air ions became 1.2 : 1, leading to a surrounding of positive air ions in human living environment. Therefore, it is urgent to adopt effective methods to improve the proportion of negative oxygen ions, which are known as “air vitamin”. In this study, negative oxygen ions production by the TiO2/Cu2O-treated wood under UV irradiation was first reported. Anatase TiO2 particles with Cu2O particles were doped on wooden substrates through a two-step method and further modification is employed to create remarkable superamphiphobic surface. The effect of Cu2O particles dopant on the negative oxygen ions production of the TiO2-treated wood was investigated. The results showed that the production of negative oxygen ions was drastically improved by doping with Cu2O particles under UV irradiation. The wood modified with TiO2/Cu2O composite film after hydrophobization is imparted with superamphiphobicity, antibacterial actions against Escherichia coli, and negative oxygen ions production under UV irradiation. PMID:27229763

  15. Negative Oxygen Ions Production by Superamphiphobic and Antibacterial TiO2/Cu2O Composite Film Anchored on Wooden Substrates.

    PubMed

    Gao, Likun; Qiu, Zhe; Gan, Wentao; Zhan, Xianxu; Li, Jian; Qiang, Tiangang

    2016-01-01

    According to statistics, early in the 20th century, the proportion of positive and negative air ions on the earth is 1 : 1.2. However, after more than one century, the equilibrium state of the proportion had an obvious change, which the proportion of positive and negative air ions became 1.2 : 1, leading to a surrounding of positive air ions in human living environment. Therefore, it is urgent to adopt effective methods to improve the proportion of negative oxygen ions, which are known as "air vitamin". In this study, negative oxygen ions production by the TiO2/Cu2O-treated wood under UV irradiation was first reported. Anatase TiO2 particles with Cu2O particles were doped on wooden substrates through a two-step method and further modification is employed to create remarkable superamphiphobic surface. The effect of Cu2O particles dopant on the negative oxygen ions production of the TiO2-treated wood was investigated. The results showed that the production of negative oxygen ions was drastically improved by doping with Cu2O particles under UV irradiation. The wood modified with TiO2/Cu2O composite film after hydrophobization is imparted with superamphiphobicity, antibacterial actions against Escherichia coli, and negative oxygen ions production under UV irradiation. PMID:27229763

  16. Negative Oxygen Ions Production by Superamphiphobic and Antibacterial TiO2/Cu2O Composite Film Anchored on Wooden Substrates

    NASA Astrophysics Data System (ADS)

    Gao, Likun; Qiu, Zhe; Gan, Wentao; Zhan, Xianxu; Li, Jian; Qiang, Tiangang

    2016-05-01

    According to statistics, early in the 20th century, the proportion of positive and negative air ions on the earth is 1 : 1.2. However, after more than one century, the equilibrium state of the proportion had an obvious change, which the proportion of positive and negative air ions became 1.2 : 1, leading to a surrounding of positive air ions in human living environment. Therefore, it is urgent to adopt effective methods to improve the proportion of negative oxygen ions, which are known as “air vitamin”. In this study, negative oxygen ions production by the TiO2/Cu2O-treated wood under UV irradiation was first reported. Anatase TiO2 particles with Cu2O particles were doped on wooden substrates through a two-step method and further modification is employed to create remarkable superamphiphobic surface. The effect of Cu2O particles dopant on the negative oxygen ions production of the TiO2-treated wood was investigated. The results showed that the production of negative oxygen ions was drastically improved by doping with Cu2O particles under UV irradiation. The wood modified with TiO2/Cu2O composite film after hydrophobization is imparted with superamphiphobicity, antibacterial actions against Escherichia coli, and negative oxygen ions production under UV irradiation.

  17. The uranium from seawater program at PNNL: Overview of marine testing, adsorbent characterization, adsorbent durability, adsorbent toxicity, and deployment studies

    DOE PAGES

    Gill, Gary A.; Kuo, Li -Jung; Janke, Christopher James; Park, Jiyeon; Jeters, Robert T.; Bonheyo, George T.; Pan, Horng -Bin; Wai, Chien; Khangaonkar, Tarang P.; Bianucci, Laura; et al

    2016-02-07

    at Woods Hole Oceanographic Institution with the ORNL AF1 adsorbent produced 15% and 55% higher adsorption capacities than observed at PNNL for column and flume testing, respectively. Variations in competing ions may be the explanation for the regional differences. In addition to marine testing, a number of other efforts are underway to characterize adsorbents and impacts of deployment on the marine environment. Highlights include: Hydrodynamic modelling predicts that a farm of adsorbent materials will likely have minimal effect on ocean currents and removal of uranium and other elements from seawater when densities are < 1800 braids/km2. A decrease in U adsorption capacity of up to 30% was observed after 42 days of exposure due to biofouling when the ORNL braided adsorbent AI8 was exposed to raw seawater in a flume in the presence of light. An identical raw seawater exposure with no light exposure showed little or no impact to adsorption capacity from biofouling. No toxicity was observed with column effluents of any absorbent materials tested to date. Toxicity could be induced with some non amidoxime-based absorbents only when the ratio of solid absorbent to test media was increased to highly unrealistic levels. Thermodynamic modeling of the seawater-amidoxime adsorbent was performed using the geochemical modeling program PHREEQC. Modeling of the binding of Ca, Mg, Fe, Ni, Cu, U, and V from batch interactions with seawater across a variety of concentrations of the amidoxime binding group reveal that when binding sites are limited (1 x 10-8 binding sites/kg seawater), vanadium heavily out-competes other ions for the amidoxime sites. In contrast, when binding sites are abundant magnesium and calcium dominate the total percentage of metals bound to the sorbent.« less

  18. Observations of Oxygen Ion Behavior in the Lithium-Based Electrolytic Reduction of Uranium Oxide

    SciTech Connect

    Steven D. Herrmann; Shelly X. Li; Brenda E. Serrano-Rodriguez

    2009-09-01

    Parametric studies were performed on a lithium-based electrolytic reduction process at bench-scale to investigate the behavior of oxygen ions in the reduction of uranium oxide for various electrochemical cell configurations. Specifically, a series of eight electrolytic reduction runs was performed in a common salt bath of LiCl – 1 wt% Li2O. The variable parameters included fuel basket containment material (i.e., stainless steel wire mesh and sintered stainless steel) and applied electrical charge (i.e., 75 – 150% of the theoretical charge for complete reduction of uranium oxide in a basket to uranium metal). Samples of the molten salt electrolyte were taken at regular intervals throughout each run and analyzed to produce a time plot of Li2O concentrations in the bulk salt over the course of the runs. Following each run, the fuel basket was sectioned and the fuel was removed. Samples of the fuel were analyzed for the extent of uranium oxide reduction to metal and for the concentration of salt constituents, i.e., LiCl and Li2O. Extents of uranium oxide reduction ranged from 43 – 70% in stainless steel wire mesh baskets and 8 – 33 % in sintered stainless steel baskets. The concentrations of Li2O in the salt phase of the fuel product from the stainless steel wire mesh baskets ranged from 6.2 – 9.2 wt%, while those for the sintered stainless steel baskets ranged from 26 – 46 wt%. Another series of tests was performed to investigate the dissolution of Li2O in LiCl at 650 °C across various cathode containment materials (i.e., stainless steel wire mesh, sintered stainless steel and porous magnesia) and configurations (i.e., stationary and rotating cylindrical baskets). Dissolution of identical loadings of Li2O particulate reached equilibrium within one hour for stationary stainless steel wire mesh baskets, while the same took several hours for sintered stainless steel and porous magnesia baskets. Rotation of an annular cylindrical basket of stainless steel

  19. Macrophages Under Low Oxygen Culture ConditionsRespond to Ion Parametric Resonance Magnetic Fields

    EPA Science Inventory

    Macrophages, when entering inflamed tissue, encounter low oxygen tension due to the impairment of blood supply and/or the massive infiltration of cells that consume oxygen. Previously, we showed that such macrophages release more bacteriotoxic hydrogen peroxide (H202) when expose...

  20. Macrophages Under Low Oxygen Culture Conditions Respond to Ion Parametric Resonance Magnetic Fields

    EPA Science Inventory

    Macrophages, when entering inflamed tissue, encounter low oxygen tension due to the impairment of blood supply and/or the massive infiltration of cells that consume oxygen. Previously, we showed that such macrophages release more bacteriotoxic hydrogen peroxide (H202) when expose...

  1. Arsenic(III, V) adsorption on a goethite-based adsorbent in the presence of major co-existing ions: Modeling competitive adsorption consistent with spectroscopic and molecular evidence

    NASA Astrophysics Data System (ADS)

    Kanematsu, Masakazu; Young, Thomas M.; Fukushi, Keisuke; Green, Peter G.; Darby, Jeannie L.

    2013-04-01

    Adsorption of the two oxyanions, arsenate (As(V)) and arsenite (As(III)), on a common goethite-based granular porous adsorbent is studied in the presence of major co-existing ions in groundwater (i.e., phosphate, silicic acid, sulfate, carbonate, magnesium, and calcium) and predicted using the extended triple layer model (ETLM), a dipole modified single-site triple layer surface complexation model consistent with spectroscopic and molecular evidence. Surface species of all ions were selected according to the previous ETLM studies and published experimental spectroscopic/theoretical molecular information. The adsorption equilibrium constants for all ions were determined using adsorption data obtained in single-solute systems. The adsorption equilibrium constants referenced to the site-occupancy standard state (indicated by Kθ) were compared with those for goethite in the literature if available. The values of these constants for the goethite-based adsorbent are found to be close to the values for goethite previously studied. These "constrained" adsorption equilibrium constants determined in single-solute systems were used in the ETLM to predict the competitive interactions of As(III, V) with the co-existing ions in binary-solute systems. The ETLM is capable of predicting As(III, V) adsorption in the presence of oxyanions (phosphate, silicic acid, sulfate, and carbonate). This study presents the first successful and systematic prediction of the competitive interactions of As(III, V) with these oxyanions using the ETLM. The ETLM prediction of surface (and aqueous) speciation also provides insights into the distinct adsorption behavior of As(III, V) in the presence of the oxyanions. Magnesium and calcium significantly enhanced As(V) adsorption at higher pH values, while they had little effect on As(III) adsorption. The enhanced adsorption of As(V), however, could not be predicted by the ETLM using the surface species proposed in previous ETLM studies. Further studies

  2. Modeling adsorption: Investigating adsorbate and adsorbent properties

    NASA Astrophysics Data System (ADS)

    Webster, Charles Edwin

    1999-12-01

    Surface catalyzed reactions play a major role in current chemical production technology. Currently, 90% of all chemicals are produced by heterogeneously catalyzed reactions. Most of these catalyzed reactions involve adsorption, concentrating the substrate(s) (the adsorbate) on the surface of the solid (the adsorbent). Pore volumes, accessible surface areas, and the thermodynamics of adsorption are essential in the understanding of solid surface characteristics fundamental to catalyst and adsorbent screening and selection. Molecular properties such as molecular volumes and projected molecular areas are needed in order to convert moles adsorbed to surface volumes and areas. Generally, these molecular properties have been estimated from bulk properties, but many assumptions are required. As a result, different literature values are employed for these essential molecular properties. Calculated molar volumes and excluded molecular areas are determined and tabulated for a variety of molecules. Molecular dimensions of molecules are important in the understanding of molecular exclusion as well as size and shape selectivity, diffusion, and adsorbent selection. Molecular dimensions can also be used in the determination of the effective catalytic pore size of a catalyst. Adsorption isotherms, on zeolites, (crystalline mineral oxides) and amorphous solids, can be analyzed with the Multiple Equilibrium Analysis (MEA) description of adsorption. The MEA produces equilibrium constants (Ki), capacities (ni), and thermodynamic parameters (enthalpies, ΔHi, and entropies, ΔSi) of adsorption for each process. Pore volumes and accessible surface areas are calculated from the process capacities. Adsorption isotherms can also be predicted for existing and new adsorbate-adsorbent systems with the MEA. The results show that MEA has the potential of becoming a standard characterization method for microporous solids that will lead to an increased understanding of their behavior in gas

  3. Strongly enhanced oxygen ion transport through samarium-doped CeO2 nanopillars in nanocomposite films

    DOE PAGES

    Yang, Sangmo; Lee, Shinbuhm; Jian, Jie; Zhang, Wenrui; Lu, Ping; Jia, Quanxi; Wang, Haiyan; Noh, Tae Won; Kalinin, Sergei V.; MacManus-Driscoll, Judith L.

    2015-10-08

    Enhancement of oxygen ion conductivity in oxides is important for low-temperature (<500 °C) operation of solid oxide fuel cells, sensors and other ionotronic devices. While huge ion conductivity has been demonstrated in planar heterostructure films, there has been considerable debate over the origin of the conductivity enhancement, in part because of the difficulties of probing buried ion transport channels. Here we create a practical geometry for device miniaturization, consisting of highly crystalline micrometre-thick vertical nanocolumns of Sm-doped CeO2 embedded in supporting matrices of SrTiO3. The ionic conductivity is higher by one order of magnitude than plain Sm-doped CeO2 films. Bymore » using scanning probe microscopy, we show that the fast ion-conducting channels are not exclusively restricted to the interface but also are localized at the Sm-doped CeO2 nanopillars. This work offers a pathway to realize spatially localized fast ion transport in oxides of micrometre thickness.« less

  4. Strongly enhanced oxygen ion transport through samarium-doped CeO2 nanopillars in nanocomposite films.

    PubMed

    Yang, Sang Mo; Lee, Shinbuhm; Jian, Jie; Zhang, Wenrui; Lu, Ping; Jia, Quanxi; Wang, Haiyan; Noh, Tae Won; Kalinin, Sergei V; MacManus-Driscoll, Judith L

    2015-10-08

    Enhancement of oxygen ion conductivity in oxides is important for low-temperature (<500 °C) operation of solid oxide fuel cells, sensors and other ionotronic devices. While huge ion conductivity has been demonstrated in planar heterostructure films, there has been considerable debate over the origin of the conductivity enhancement, in part because of the difficulties of probing buried ion transport channels. Here we create a practical geometry for device miniaturization, consisting of highly crystalline micrometre-thick vertical nanocolumns of Sm-doped CeO2 embedded in supporting matrices of SrTiO3. The ionic conductivity is higher by one order of magnitude than plain Sm-doped CeO2 films. By using scanning probe microscopy, we show that the fast ion-conducting channels are not exclusively restricted to the interface but also are localized at the Sm-doped CeO2 nanopillars. This work offers a pathway to realize spatially localized fast ion transport in oxides of micrometre thickness.

  5. Strongly enhanced oxygen ion transport through samarium-doped CeO2 nanopillars in nanocomposite films.

    PubMed

    Yang, Sang Mo; Lee, Shinbuhm; Jian, Jie; Zhang, Wenrui; Lu, Ping; Jia, Quanxi; Wang, Haiyan; Noh, Tae Won; Kalinin, Sergei V; MacManus-Driscoll, Judith L

    2015-01-01

    Enhancement of oxygen ion conductivity in oxides is important for low-temperature (<500 °C) operation of solid oxide fuel cells, sensors and other ionotronic devices. While huge ion conductivity has been demonstrated in planar heterostructure films, there has been considerable debate over the origin of the conductivity enhancement, in part because of the difficulties of probing buried ion transport channels. Here we create a practical geometry for device miniaturization, consisting of highly crystalline micrometre-thick vertical nanocolumns of Sm-doped CeO2 embedded in supporting matrices of SrTiO3. The ionic conductivity is higher by one order of magnitude than plain Sm-doped CeO2 films. By using scanning probe microscopy, we show that the fast ion-conducting channels are not exclusively restricted to the interface but also are localized at the Sm-doped CeO2 nanopillars. This work offers a pathway to realize spatially localized fast ion transport in oxides of micrometre thickness. PMID:26446866

  6. Strongly enhanced oxygen ion transport through samarium-doped CeO2 nanopillars in nanocomposite films

    PubMed Central

    Yang, Sang Mo; Lee, Shinbuhm; Jian, Jie; Zhang, Wenrui; Lu, Ping; Jia, Quanxi; Wang, Haiyan; Won Noh, Tae; Kalinin, Sergei V.; MacManus-Driscoll, Judith L.

    2015-01-01

    Enhancement of oxygen ion conductivity in oxides is important for low-temperature (<500 °C) operation of solid oxide fuel cells, sensors and other ionotronic devices. While huge ion conductivity has been demonstrated in planar heterostructure films, there has been considerable debate over the origin of the conductivity enhancement, in part because of the difficulties of probing buried ion transport channels. Here we create a practical geometry for device miniaturization, consisting of highly crystalline micrometre-thick vertical nanocolumns of Sm-doped CeO2 embedded in supporting matrices of SrTiO3. The ionic conductivity is higher by one order of magnitude than plain Sm-doped CeO2 films. By using scanning probe microscopy, we show that the fast ion-conducting channels are not exclusively restricted to the interface but also are localized at the Sm-doped CeO2 nanopillars. This work offers a pathway to realize spatially localized fast ion transport in oxides of micrometre thickness. PMID:26446866

  7. Strongly enhanced oxygen ion transport through samarium-doped CeO2 nanopillars in nanocomposite films

    SciTech Connect

    Yang, Sangmo; Lee, Shinbuhm; Jian, Jie; Zhang, Wenrui; Lu, Ping; Jia, Quanxi; Wang, Haiyan; Noh, Tae Won; Kalinin, Sergei V.; MacManus-Driscoll, Judith L.

    2015-10-08

    Enhancement of oxygen ion conductivity in oxides is important for low-temperature (<500 °C) operation of solid oxide fuel cells, sensors and other ionotronic devices. While huge ion conductivity has been demonstrated in planar heterostructure films, there has been considerable debate over the origin of the conductivity enhancement, in part because of the difficulties of probing buried ion transport channels. Here we create a practical geometry for device miniaturization, consisting of highly crystalline micrometre-thick vertical nanocolumns of Sm-doped CeO2 embedded in supporting matrices of SrTiO3. The ionic conductivity is higher by one order of magnitude than plain Sm-doped CeO2 films. By using scanning probe microscopy, we show that the fast ion-conducting channels are not exclusively restricted to the interface but also are localized at the Sm-doped CeO2 nanopillars. This work offers a pathway to realize spatially localized fast ion transport in oxides of micrometre thickness.

  8. Is the surface oxygen exchange rate linked to bulk ion diffusivity in mixed conducting Ruddlesden–Popper phases?

    SciTech Connect

    Tomkiewicz, Alex C.; Tamimi, Mazin A.; Huq, Ashfia; McIntosh, Steven

    2015-03-02

    There is a possible link between oxygen surface exchange rate and bulk oxygen anion diffusivity in mixed ionic and electronic conducting oxides; it is a topic of great interest and debate. While a large body of experimental evidence and theoretical analyses support a link, observed differences between bulk and surface composition of these materials are hard to reconcile with this observation. This is further compounded by potential problems with simultaneous measurement of both parameters. Here we utilize separate techniques, in situ neutron diffraction and pulsed isotopic surface exchange, to examine bulk ion mobility and surface oxygen exchange rates of three Ruddlesden-Popper phases, general form An-1A2'BnO3n+1, An-1A2'BnX3n+1; LaSrCo0.5Fe0.5O4-δ (n = 1), La0.3Sr2.7CoFeO7-δ (n = 2) and LaSr3Co1.5Fe1.5O10-δ (n = 3). These measurements are complemented by surface composition determination via high sensitivity-low energy ion scattering. We observe a correlation between bulk ion mobility and surface exchange rate between materials. The surface exchange rates vary by more than one order of magnitude with high anion mobility in the bulk of an oxygen vacancy-rich n = 2 Ruddlesden-Popper material correlating with rapid oxygen exchange. Furthermore this is in contrast with the similar surface exchange rates which we may expect due to similar surface compositions across all three samples. This paper conclude that experimental limitations lead to inherent convolution of surface and bulk rates, and that surface exchange steps are not likely to be rate limiting in oxygen incorporation.

  9. Oxygen-18 study of the mechanism of promoter action of thiocyanate ions in the electrosynthesis of persulfuric acid and ammonium persulfate at platinum anodes

    SciTech Connect

    Kasatkin, E.V.; Larchenko, L.I.; Potapova, G.F.

    1987-02-01

    The authors use labelled oxygen to study the involvement of water and sulfate ions in molecular oxygen evolution during the anodic synthesis of persulfuric acid and ammonium persulfate at a platinum anode in an electrolytic cell with and without thiocyanate as a promoter for the electrocatalytic reaction.

  10. Effect of 100MeV oxygen ion irradiation on silicon NPN power transistor

    NASA Astrophysics Data System (ADS)

    Kumar, M. Vinay; Krishnakumar, K. S.; Dinesh, C. M.; Krishnaveni, S.; Ramani

    2012-06-01

    The radiation response of npn Bipolar junction transistor (BJT) has been examined for 100 MeV O7+ ion. Key electrical properties like Gummel characteristics, dc current gain and capacitance-voltage of 100MeV O7+ ion irradiated transistor were studied before and after irradiation. The device was decapped and the electrical characterizations were performed at room temperature. Base current is observed to be more sensitive than collector current and gain appears to be degraded with ion fluence, also considerable degradation in C-V characteristics is observed and doping concentration is found to be increased along with the increase in ion fluence.

  11. Lattice damage and waveguide properties of a proton-exchanged LiNbO3 crystal after oxygen-ion implantation

    NASA Astrophysics Data System (ADS)

    Huang, Qing; Liu, Peng; Liu, Tao; Guo, Sha-Sha; Zhang, Lian; Wang, Xue-Lin

    2012-09-01

    A z-cut LiNbO3 crystal was immersed in a molten benzoic acid for 10 min and then was implanted with 6-MeV oxygen ions at a fluence of 6 × 1014 ions/cm2. Lattice damage in this crystal was measured by a Rutherford backscattering and channeling technique and was compared with lattice damage in a proton-exchanged LiNbO3 crystal and an oxygen-ion-implanted LiNbO3 crystal. A totally amorphous layer was formed at the crystal's surface after both proton exchange and oxygen-ion implantation processes were performed, even though either process alone never led to a relative disorder of the lattice up to 0.2. It indicates that the crystal lattice in the proton-exchanged layer is unstable and can be easily damaged by ion implantation subsequently. The waveguide structure formed by proton exchange was destroyed by oxygen-ion implantation. Oxygen-ion implantation induced an increase in extraordinary refractive index and formed another waveguide structure underneath the amorphous surface layer.

  12. Oxygen loss induced by swift heavy ions of low and high dE/dx in PMMA thin films

    NASA Astrophysics Data System (ADS)

    Thomaz, R.; Gutierres, L. I.; Morais, J.; Louette, P.; Severin, D.; Trautmann, C.; Pireaux, J. J.; Papaléo, R. M.

    2015-12-01

    Investigations on the chemical modifications induced by swift heavy ions in PMMA thin films were carried out using beams of high dE/dx (2.2 GeV Bi, 14,090 eV/nm) and low dE/dx (2 MeV H, 19 eV/nm). The induced chemical modifications were monitored by XPS for films with initial thickness of 50 and 100 nm. For both beams, the irradiation decreased the amount of carbon atoms bound to oxygen (Cdbnd O and Csbnd Osbnd C), with a larger decrease of the carboxyl moiety, as expected. However, the chemical changes induced by light and heavy ions were qualitatively different. For the same mean deposited energy density, proton irradiation induced a decrease of the relative intensity of the carbon-oxygen bonds up to ∼20% larger than the irradiation with Bi ions. This suggests a greater importance of particle ejection by unzipping of PMMA chains at high dE/dx, which tends to keep the O/C ratio closer to the pristine value.

  13. Electron-Stimulated Oxidation of Thin Water Films Adsorbed on TiO2(110)

    SciTech Connect

    Lane, Christopher D.; Petrik, Nikolay G.; Orlando, Thomas M.; Kimmel, Greg A.

    2007-11-08

    Electron-stimulated reactions in thin (< 3 monolayer, ML) water films adsorbed on TiO2(110) are investigated. For electron fluences less than ~1×1016 e-/cm2, irradiation with 100 eV electrons results in electron-stimulated desorption (ESD) of atomic and molecular hydrogen, but no measurable O2. The ESD leaves adsorbed hydroxyls which oxidize the TiO2(110) surface and change the post-irradiation TPD spectra of the remaining water in characteristic ways. The species remaining on the TiO2(110) after irradiation of adsorbed water films are apparently similar to those produced without irradiation by co-dosing water and O2. Annealing above ~600 K reduces the oxidized surfaces, and water TPD spectra characteristic of ion sputtered and annealed TiO2(110) are recovered. The rate of electron-stimulated “oxidation” of the water films is proportional to the coverage of water in the first layer for coverages less than 1 ML. However, higher coverages suppress this reaction. When thin water films are irradiated, the rate of electron-stimulated oxidation is independent of the initial oxygen vacancy concentration, as is the final oxidized state achieved at high electron fluences. To explain the results, we propose that electron excitation of water molecules adsorbed on Ti4+ sites leads to desorption of hydrogen atoms and leaves an OH adsorbed at the site. If hydroxyls are present in the bridging oxygen rows, these react with the OH’s on the Ti4+ sites to reform water and heal the oxygen vacancy associated with the bridging OH. Once the bridge bonded hydroxyls have been eliminated, further irradiation increases the concentration of OH’s in the Ti4+ rows leading to the creation of species which block sites in the Ti4+ rows, perhaps H2O2 and/or HO2.

  14. Extraction of methocarbamol from human plasma with a polypyrrole/multiwalled carbon nanotubes composite decorated with magnetic nanoparticles as an adsorbent followed by electrospray ionization ion mobility spectrometry detection.

    PubMed

    Saraji, Mohammad; Khayamian, Taghi; Hashemian, Zahra

    2014-12-01

    In this work, a polypyrrole/multiwalled carbon nanotubes composite decorated with Fe3 O4 nanoparticles was chemically synthesized and applied as a novel adsorbent for the extraction of methocarbamol from human plasma. Electrospray ionization ion mobility spectrometry was used for the determination of the analyte. The properties of the magnetic-modified adsorbent were characterized by scanning electron microscopy, transmission electron microscopy, Fourier transform IR spectroscopy, and X-ray diffraction. The effects of experimental parameters on the extraction efficiency of the sorbent were investigated. Under the optimized conditions, the linear dynamic range was found to be 2-150 ng/mL with the detection limit of 0.9 ng/mL. The relative standard deviation was 5.3% for three replicate measurements of methocarbamol in plasma sample. The extraction efficiency of the sorbent for the determination of different drugs with various polarities was also compared to that of Fe3 O4 -polypyrrole and Fe3 O4 -multiwalled carbon nanotubes sorbents. Finally, the method was used for the determination of methocarbamol in blood samples. PMID:25243817

  15. Extraction of methocarbamol from human plasma with a polypyrrole/multiwalled carbon nanotubes composite decorated with magnetic nanoparticles as an adsorbent followed by electrospray ionization ion mobility spectrometry detection.

    PubMed

    Saraji, Mohammad; Khayamian, Taghi; Hashemian, Zahra

    2014-12-01

    In this work, a polypyrrole/multiwalled carbon nanotubes composite decorated with Fe3 O4 nanoparticles was chemically synthesized and applied as a novel adsorbent for the extraction of methocarbamol from human plasma. Electrospray ionization ion mobility spectrometry was used for the determination of the analyte. The properties of the magnetic-modified adsorbent were characterized by scanning electron microscopy, transmission electron microscopy, Fourier transform IR spectroscopy, and X-ray diffraction. The effects of experimental parameters on the extraction efficiency of the sorbent were investigated. Under the optimized conditions, the linear dynamic range was found to be 2-150 ng/mL with the detection limit of 0.9 ng/mL. The relative standard deviation was 5.3% for three replicate measurements of methocarbamol in plasma sample. The extraction efficiency of the sorbent for the determination of different drugs with various polarities was also compared to that of Fe3 O4 -polypyrrole and Fe3 O4 -multiwalled carbon nanotubes sorbents. Finally, the method was used for the determination of methocarbamol in blood samples.

  16. Nuclear tracks in CR-39 produced by carbon, oxygen, aluminium and titanium ions.

    PubMed

    Rickards, J; Romo, V; Golzarri, J I; Espinosa, G

    2002-01-01

    This work describes the response of CR-39 (allyl diglycol polycarbonate) to different ions (C, O, Al and Ti) produced by the Instituto de Fisica 3 MV 9SDH-2 Pelletron accelerator and backscattered from a thin Au film on a C support. The ion energies were chosen in series such that the ranges of the different ions in the detector were 2, 3, 4, 5, 6, 7 and 8 microm respectively for each series. Once exposed, the detectors were etched with a solution of 6.25 M KOH at 60 degrees C, and the reading was carried out using a digital image analysis system. An analysis of the measured track diameters of all the types of ions indicates that, for a given range, track kinetics are independent of type of ion, energy and stopping power.

  17. Influence of temperature on oxygen permeation through ion transport membrane to feed a biomass gasifier

    NASA Astrophysics Data System (ADS)

    Antonini, T.; Foscolo, P. U.; Gallucci, K.; Stendardo, S.

    2015-11-01

    Oxygen-permeable perovskite membranes with mixed ionic-electronic conducting properties can play an important role in the high temperature separation of oxygen from air. A detailed design of a membrane test module is presented, useful to test mechanical resistance and structural stability of Ba0.5Sr0.5Co0.8Fe0.2O3-δ (BSCF) capillary membrane in the reactor environment. Preliminary experimental results of membrane permeation tests highlight the positive effect of temperature on perovskite materials. This behaviour is also confirmed by a computational model of char combustion with oxygen permeated through the membrane module, when it is placed inside a gasifier reactor to provide the necessary input of heat to the gasification endothermic process. The results show that the temperature affects the oxygen permeation of the BSCF membrane remarkably.

  18. Treatment effect of the method of Tai Chi exercise in combination with inhalation of air negative oxygen ions on hyperlipidemia

    PubMed Central

    Ma, Ming; Song, Qing-Hua; Xu, Rong-Mei; Zhang, Quan-Hai; Shen, Guo-Qing; Guo, Yan-Hua; Wang, Yi

    2014-01-01

    Objective: To observe the improvement effect of the treatment method of Tai Chi exercise in combination with inhalation of the air negative oxygen ions on the blood lipid indicator of the patient suffering from the hyperlipidemia. Methods: 56 patients, who are diagnosed with hyperlipidemia, are the study objects and divided into an observation group and a control group by the random number method. Each group consists of 28 patients. The patients in the control group do Tai Chi exercise for about 60 min once a day; the patients in the observation group, in addition to Tai Chi exercise, are treated by inhalation of the air negative oxygen ions. Before the treatment and after 6 months’ treatment, respectively test and compare body fat content, blood lipid, blood rheology and psychological adaptation as well as other indicators for these two groups of patients. Results: In comparison with the ordinary materials of the patients in two groups before the treatment, it shows no significant difference, P>0.05; after they are respectively treated for 6 months, it is found that the testing indicators of the patients in two groups are improved to some extent, but those of the observation group are better. Compared with the improvement effect of the control group, the difference has statistical significance, P<0.05. Conclusion: Tai Chi Exercise can improve the blood lipid indicator of the patient suffering from hyperlipidemia to some extent, however, the treatment method, in combination with inhalation of air negative oxygen ion, can obtain better effect than that of single Tai Chi exercise. Tip: the environment of the exercise plays an important intervention role in the treatment effect. PMID:25232426

  19. General facile approach to transition-metal oxides with highly uniform mesoporosity and their application as adsorbents for heavy-metal-ion sequestration.

    PubMed

    Seisenbaeva, Gulaim A; Daniel, Geoffrey; Kessler, Vadim G; Nedelec, Jean-Marie

    2014-08-18

    Mesoporous powders of transition-metal oxides, TiO2, ZrO2, HfO2, Nb2O5, and Ta2O5, pure from organic impurities were produced by a rapid single-step thermohydrolytic approach. The obtained materials display an impressively large active surface area and sharp pore-size distribution, being composed of partially coalesced uniform nanoparticles with crystalline cores and amorphous shells. They reveal extremely high adsorption capacity in removal of Cr(VI) anions from solutions (25.8 for TiO2, 73.0 for ZrO2, and 74.7 mg g(-1) for Nb2O5 in relation to the Cr2O7(2-) anion), making them very attractive as adsorbents in water remediation applications. The difference in adsorption capacities for the studied oxides may be explained by variation in surface hydration and surface-charge distribution.

  20. Simultaneous determination of copper, cobalt, and mercury ions in water samples by solid-phase extraction using carbon nanotube sponges as adsorbent after chelating with sodium diethyldithiocarbamate prior to high performance liquid chromatography.

    PubMed

    Wang, Lei; Zhou, Jia-Bin; Wang, Xia; Wang, Zhen-Hua; Zhao, Ru-Song

    2016-06-01

    Recently, a sponge-like material called carbon nanotube sponges (CNT sponges) has drawn considerable attention because it can remove large-area oil, nanoparticles, and organic dyes from water. In this paper, the feasibility of CNT sponges as a novel solid-phase extraction (SPE) adsorbent for the enrichment and determination of heavy metal ions (Co(2+), Cu(2+), and Hg(2+)) was investigated for the first time. Sodium diethyldithiocarbamate (DDTC) was used as the chelating agent and high performance liquid chromatography (HPLC) for the final analysis. Important factors which may influence extraction efficiency of SPE were optimized, such as the kind and volume of eluent, volume of DDTC, sample pH, flow rate, etc. Under the optimized conditions, wide range of linearity (0.5-400 μg L(-1)), low limits of detection (0.089~0.690 μg L(-1); 0.018~0.138 μg), and good repeatability (1.27~3.60 %, n = 5) were obtained. The developed method was applied for the analysis of the three metal ions in real water samples, and satisfactory results were achieved. All of these findings demonstrated that CNT sponges will be a good choice for the enrichment and determination of target ions at trace levels in the future. PMID:27108287

  1. Redox-inactive metal ions promoted the catalytic reactivity of non-heme manganese complexes towards oxygen atom transfer.

    PubMed

    Choe, Cholho; Yang, Ling; Lv, Zhanao; Mo, Wanling; Chen, Zhuqi; Li, Guangxin; Yin, Guochuan

    2015-05-21

    Redox-inactive metal ions can modulate the reactivity of redox-active metal ions in a variety of biological and chemical oxidations. Many synthetic models have been developed to help address the elusive roles of these redox-inactive metal ions. Using a non-heme manganese(II) complex as the model, the influence of redox-inactive metal ions as a Lewis acid on its catalytic efficiency in oxygen atom transfer was investigated. In the absence of redox-inactive metal ions, the manganese(II) catalyst is very sluggish, for example, in cyclooctene epoxidation, providing only 9.9% conversion with 4.1% yield of epoxide. However, addition of 2 equiv. of Al(3+) to the manganese(II) catalyst sharply improves the epoxidation, providing up to 97.8% conversion with 91.4% yield of epoxide. EPR studies of the manganese(II) catalyst in the presence of an oxidant reveal a 16-line hyperfine structure centered at g = 2.0, clearly indicating the formation of a mixed valent di-μ-oxo-bridged diamond core, Mn(III)-(μ-O)2-Mn(IV). The presence of a Lewis acid like Al(3+) causes the dissociation of this diamond Mn(III)-(μ-O)2-Mn(IV) core to form monomeric manganese(iv) species which is responsible for improved epoxidation efficiency. This promotional effect has also been observed in other manganese complexes bearing various non-heme ligands. The findings presented here have provided a promising strategy to explore the catalytic reactivity of some di-μ-oxo-bridged complexes by adding non-redox metal ions to in situ dissociate those dimeric cores and may also provide clues to understand the mechanism of methane monooxygenase which has a similar diiron diamond core as the intermediate.

  2. Oxygen defects in phosphorene.

    PubMed

    Ziletti, A; Carvalho, A; Campbell, D K; Coker, D F; Castro Neto, A H

    2015-01-30

    Surface reactions with oxygen are a fundamental cause of the degradation of phosphorene. Using first-principles calculations, we show that for each oxygen atom adsorbed onto phosphorene there is an energy release of about 2 eV. Although the most stable oxygen adsorbed forms are electrically inactive and lead only to minor distortions of the lattice, there are low energy metastable forms which introduce deep donor and/or acceptor levels in the gap. We also propose a mechanism for phosphorene oxidation involving reactive dangling oxygen atoms and we suggest that dangling oxygen atoms increase the hydrophilicity of phosphorene.

  3. A comparative study of 30MeV boron{sup 4+} and 60MeV oxygen{sup 8+} ion irradiated Si NPN BJTs

    SciTech Connect

    Kumar, M. Vinay Krishnaveni, S.; Yashoda, T.; Dinesh, C. M.; Krishnakumar, K. S.; Jayashree, B.; Ramani

    2015-06-24

    The impact of 30MeV boron{sup 4+} and 60MeV oxygen{sup 8+} ion irradiation on electrical characteristics of 2N3773 Si NPN Bipolar junction transistors (BJTs) is reported in the present study. The transistors were decapped and irradiated at room temperature. Gummel characteristics, DC current gain and Capacitance-voltage (C-V) characteristics were studied before and after irradiation at different fluences. DC current gain has decreased significantly in both boron and oxygen ion irradiation. Also the value of capacitance decreased 3-4 times with increase in fluence. Both 30MeV boron ion and 60MeV oxygen ion induced similar extent of degradation in electrical characteristics of the transistor.

  4. A comparative study of 30MeV boron4+ and 60MeV oxygen8+ ion irradiated Si NPN BJTs

    NASA Astrophysics Data System (ADS)

    Kumar, M. Vinay; Yashoda, T.; Dinesh, C. M.; Krishnakumar, K. S.; Jayashree, B.; Ramani, Krishnaveni, S.

    2015-06-01

    The impact of 30MeV boron4+ and 60MeV oxygen8+ ion irradiation on electrical characteristics of 2N3773 Si NPN Bipolar junction transistors (BJTs) is reported in the present study. The transistors were decapped and irradiated at room temperature. Gummel characteristics, DC current gain and Capacitance-voltage (C-V) characteristics were studied before and after irradiation at different fluences. DC current gain has decreased significantly in both boron and oxygen ion irradiation. Also the value of capacitance decreased 3-4 times with increase in fluence. Both 30MeV boron ion and 60MeV oxygen ion induced similar extent of degradation in electrical characteristics of the transistor.

  5. The precipitation of keV energetic oxygen ions at Mars and their effects during the comet Siding Spring approach

    NASA Astrophysics Data System (ADS)

    Gronoff, G.; Rahmati, A.; Simon Wedlund, C.; Mertens, C. J.; Cravens, T.; Kallio, E. J.; Pawlowski, D. J.; Bell, J. M.

    2014-12-01

    On October 19, 2014, the Siding Spring C/2013 A1 comet passed in the vicinity of Mars with a closest approach of ˜sim130,000 km with a heliocentric distance of 1.38 AU.The coma of the comet interacted with Mars, leading to the precipitation of molecules, ions, and dust particles. The most important atmospheric effect was the precipitation of atoms/molecules/ions, and especially atomic oxygen atoms and O+^+ ions. Although the main gas forming the corona of comets is H2_2O, the cometary coronal gas is partially ionized and dissociated by the EUV-XUV solar flux. To understand the atomic and molecular precipitation effects during such an encounter, it is therefore necessary to evaluate the flux of the neutral gas ejected from the comet, and to compute its composition after the dissociation/ionization. We computed the photodissociation of the cometary gas for different solar conditions, and for the conditions of the comet encounter. In addition, using a pickup ion code, we computed the fluxes of the O+^+ ions accelerated by the solar wind at energies greated than a keV. Using the Planetocosmic model, we computed the ionization in the atmosphere of Mars due to these species, and, using the M-GITM model, we computed the associated increase of the ion/electron density.For the first time, an estimate of the flux of energetic O+^+ ions picked up by the solar wind from the cometary coma is shown, with an increase of the O+^+ flux above 50 keV by two orders of magnitude. While the ionization of Mars' upper atmosphere by precipitating O+^+ ions is expected to be negligible compared to solar EUV-XUV ionization, it is of the same order of magnitude at 110 km altitude during the cometary passage.The present work will show both the theoretical results of the ion interaction with the upper atmosphere of Mars and the results of the observations.

  6. UV-vis spectroscopy of iodine adsorbed on alkali-metal-modified zeolite catalysts for addition of carbon dioxide to ethylene oxide

    SciTech Connect

    Doskocil, E.J.; Bordawekar, S.V.; Kaye, B.G.; Davis, R.J.

    1999-07-29

    The basicity of alkali-metal-exchange (Na, K, Cs) zeolites X and Y was probed by UV-vis diffuse reflectance spectroscopy of adsorbed iodine. The observed blue shift in the visible absorption spectrum of adsorbed iodine, compared to gaseous iodine, correlated well with the negative charge on the framework oxygen atoms calculated from the Sanderson electronegativity equalization principle. The blue shifts associated with iodine adsorbed on classical catalytic supports like silica, alumina, and magnesia suggest that the iodine adsorption technique for probing basicity is applicable to a wide variety of solids. Iodine was also adsorbed on X and Y zeolites containing occluded cesium oxide formed by decomposition of impregnated cesium acetate. However, the iodine appeared to irreversibly react on these strongly basic samples, possibly forming an adsorbed triiodide ions. As a complement to the adsorption studies, the activity of alkali-metal-containing zeolites for the base-catalyzed formation of ethylene carbonate from ethylene oxide and carbon dioxide was investigated. Among the ion-exchanged zeolites, the cesium form of zeolite X exhibited the highest activity for ethylene carbonate formation. The catalytic activity of a zeolite containing occluded cesium was even higher than that of a cesium-exchanged zeolite. The presence of water adsorbed in zeolite pores promoted the rate of ethylene carbonate formation for both cesium-exchanged and cesium-impregnated zeolite X.

  7. Oxygen deficiency and salinity affect cell-specific ion concentrations in adventitious roots of barley (Hordeum vulgare).

    PubMed

    Kotula, Lukasz; Clode, Peta L; Striker, Gustavo G; Pedersen, Ole; Läuchli, André; Shabala, Sergey; Colmer, Timothy D

    2015-12-01

    Oxygen deficiency associated with soil waterlogging adversely impacts root respiration and nutrient acquisition. We investigated the effects of O2 deficiency and salinity (100 mM NaCl) on radial O2 concentrations and cell-specific ion distributions in adventitious roots of barley (Hordeum vulgare). Microelectrode profiling measured O2 concentrations across roots in aerated, aerated saline, stagnant or stagnant saline media. X-ray microanalysis at two positions behind the apex determined the cell-specific elemental concentrations of potassium (K), sodium (Na) and chloride (Cl) across roots. Severe O2 deficiency occurred in the stele and apical regions of roots in stagnant solutions. O2 deficiency in the stele reduced the concentrations of K, Na and Cl in the pericycle and xylem parenchyma cells at the subapical region. Near the root apex, Na declined across the cortex in roots from the aerated saline solution but was relatively high in all cell types in roots from the stagnant saline solution. Oxygen deficiency has a substantial impact on cellular ion concentrations in roots. Both pericycle and xylem parenchyma cells are involved in energy-dependent K loading into the xylem and in controlling radial Na and Cl transport. At root tips, accumulation of Na in the outer cell layers likely contributed to reduction of Na in inner cells of the tips.

  8. Structure and tribological performance by nitrogen and oxygen plasma based ion implantation on Ti6Al4V alloy

    NASA Astrophysics Data System (ADS)

    Feng, Xingguo; Sun, Mingren; Ma, Xinxin; Tang, Guangze

    2011-09-01

    Ti6Al4V alloy was implanted with nitrogen-oxygen mixture by using plasma based ion implantation (PBII) at pulsed voltage -10, -30 and -50 kV. The implantation was up to 6 × 1017 ions/cm2 fluence. The changes in chemical composition, structure and hardness of the modified surfaces were studied by XPS and nanoindentation measurements. According to XPS, it was found that the modified layer was predominantly TiO2, but contained small amounts of TiO, Ti2O3, TiN and Al2O3 between the outmost layer and metallic substrate. Surface hardness and wear resistance of the samples increased significantly after PBII treatment, the wear rate of the sample implanted N2-O2 mixture at -50 kV decreased eight times than the untreated one. The sample implanted N2-O2 mixture showed better wear resistance than that of the sample only implanted oxygen at - 50 kV. The wear mechanism of untreated sample was abrasive-dominated and adhesive, and the wear scar of the sample implanted at -50 kV was characterized by abrasive wear-type ploughing.

  9. Structural and Electrochemical Impacts of Oxygen Doped and Surfactant Coated Activated Carbon Electrodes in Li-ion Batteries

    NASA Astrophysics Data System (ADS)

    Collins, John; Gourdin, Gerald; Qu, Deyang; Foster, Michelle

    2013-03-01

    Passive charge and discharge dynamics are necessary for advancing Li-ion batteries. Surfactant adsorption on activated carbon has been shown to promote advancements in the discharge capacity, time and cycle-ability of electrochemical systems--specifically by enhancing diffusion pathways for ion insertion/de-insertion and suppressing pore blockage from precipitates known to form during charge/discharge states. Enhancement of surfactant chemisorption on activated carbon is achieved through oxygen doping of the carbon surface. In addition, doping alters the degree of Faradaic processes occurring in solution, resulting in prolonged reduction at the carbon surface. The work presented describes how surface oxygen groups on a granulated activated carbon have been manipulated using nitric acid in a controlled, stepwise fashion. A nonionic surfactant was applied to oxidized and non-oxidized samples at various concentrations. The composition and structure of the activated carbon surface was characterized using DRIFTS, Raman Spectroscopy, SEM and Porosimetry. The charge/discharge Li insertion capacities along with correlating surface microstructure changes were analyzed for all treated electrodes at progressive oxidation stages.

  10. Effective particle energies for stopping power calculation in radiotherapy treatment planning with protons and helium, carbon, and oxygen ions

    NASA Astrophysics Data System (ADS)

    Inaniwa, T.; Kanematsu, N.

    2016-10-01

    The stopping power ratio (SPR) of body tissues relative to water depends on the particle energy. For simplicity, however, most analytical dose planning systems do not account for SPR variation with particle energy along the beam’s path, but rather assume a constant energy for SPR estimation. The range error due to this simplification could be indispensable depending on the particle species and the assumed energy. This error can be minimized by assuming a suitable energy referred to as an ‘effective energy’ in SPR estimation. To date, however, the effective energy has never been investigated for realistic patient geometries. We investigated the effective energies for proton, helium-, carbon-, and oxygen-ion radiotherapy using volumetric models of the reference male and female phantoms provided by the International Commission on Radiological Protection (ICRP). The range errors were estimated by comparing the particle ranges calculated when particle energy variations were and were not considered. The effective energies per nucleon for protons and helium, carbon, and oxygen ions were 70 MeV, 70 MeV, 131 MeV, and 156 MeV, respectively. Using the determined effective energies, the range errors were reduced to  ⩽0.3 mm for respective particle species. For SPR estimation of multiple particle species, an effective energy of 100 MeV is recommended, with which the range error is  ⩽0.5 mm for all particle species.

  11. Nanopore reactive adsorbents for the high-efficiency removal of waste species

    DOEpatents

    Yang, Arthur Jing-Min; Zhang, Yuehua

    2005-01-04

    A nanoporous reactive adsorbent incorporates a relatively small number of relatively larger reactant, e.g., metal, enzyme, etc., particles (10) forming a discontinuous or continuous phase interspersed among and surrounded by a continuous phase of smaller adsorbent particles (12) and connected interstitial pores (14) therebetween. The reactive adsorbent can effectively remove inorganic or organic impurities in a liquid by causing the liquid to flow through the adsorbent. For example, silver ions may be adsorbed by the adsorbent particles (12) and reduced to metallic silver by reducing metal, such as ions, as the reactant particles (10). The column can be regenerated by backwashing with the liquid effluent containing, for example, acetic acid.

  12. Chemisorption of a molecular oxygen on the UN(0 0 1) surface: Ab initio calculations

    NASA Astrophysics Data System (ADS)

    Zhukovskii, Yu. F.; Bocharov, D.; Kotomin, E. A.

    2009-09-01

    The results of DFT GGA calculations on oxygen molecules adsorbed upon the (0 0 1) surface of uranium mononitride (UN) are presented and discussed. We demonstrate that O 2 molecules oriented parallel to the substrate can dissociate either (i) spontaneously when the molecular center lies above the surface hollow site or atop N ion, (ii) with the activation barrier when a molecule sits atop the surface U ion. This explains fast UN oxidation in air.

  13. Simultaneous determination of nickel, cobalt and mercury ions in water samples by solid phase extraction using multiwalled carbon nanotubes as adsorbent after chelating with sodium diethyldithiocarbamate prior to high performance liquid chromatography.

    PubMed

    Zhou, Qingxiang; Xing, An; Zhao, Kuifu

    2014-09-19

    Multiwalled carbon nanotubes (MWNTs) have been widely used for the enrichment of trace important pollutants in environment because of its large specific surface area, high extraction efficiency, and easy operation. In this study, a solid phase extraction method was established to determine nickel (Ni(2+)), cobalt (Co(2+)) and mercury (Hg(2+)) ions using MWNTs as the adsorbent and sodium diethyldithiocarbamate (DDTC) as the chelating agent. The final analysis was performed on a high performance liquid chromatography (HPLC). The factors that may influence the extraction efficiency were optimized in detail including the type and volume of elution solvent, sample pH, volume of chelating agent solution, and volume of sample solution, etc. The experimental results indicated that good linear relationship between peak area and the concentration of the ions was achieved in the range of 0.1-100μgL(-1), 0.1-50μgL(-1), and 2.7-300μgL(-1) for Ni(2+), Co(2+), and Hg(2+), respectively. The precision was determined by calculating the relative standard deviation (R.S.D.) values that were in the range of 6.2-11.7% under the optimal conditions. The detection limits of Ni(2+), Co(2+), and Hg(2+) were in the range of 0.04-0.9μgL(-1) (S/N=3). The presented method was applied for the determination of the metal ions mentioned above in real water samples, and satisfied results were achieved. All these indicated that proposed method will be a good alternative tool for monitoring the target ions in environmental samples in the future.

  14. In Situ Binding Sb Nanospheres on Graphene via Oxygen Bonds as Superior Anode for Ultrafast Sodium-Ion Batteries.

    PubMed

    Wan, Fang; Guo, Jin-Zhi; Zhang, Xiao-Hua; Zhang, Jing-Ping; Sun, Hai-Zhu; Yan, Qingyu; Han, Dong-Xue; Niu, Li; Wu, Xing-Long

    2016-03-01

    Graphene incorporation should be one effective strategy to develop advanced electrode materials for a sodium-ion battery (SIB). Herein, the micro/nanostructural Sb/graphene composite (Sb-O-G) is successfully prepared with the uniform Sb nanospheres (∼100 nm) bound on the graphene via oxygen bonds. It is revealed that the in-situ-constructed oxygen bonds play a significant role on enhancing Na-storage properties, especially the ultrafast charge/discharge capability. The oxygen-bond-enhanced Sb-O-G composite can deliver a high capacity of 220 mAh/g at an ultrahigh current density of 12 A/g, which is obviously superior to the similar Sb/G composite (130 mAh/g at 10 A/g) just without Sb-O-C bonds. It also exhibits the highest Na-storage capacity compared to Sb/G and pure Sb nanoparticles as well as the best cycling performance. More importantly, this Sb-O-G anode achieves ultrafast (120 C) energy storage in SIB full cells, which have already been shown to power a 26-bulb array and calculator. All of these superior performances originate from the structural stability of Sb-O-C bonds during Na uptake/release, which has been verified by ex situ X-ray photoelectron spectroscopies and infrared spectroscopies.

  15. EISCAT/CRRES observations: nightside ionospheric ion outflow and oxygen-rich substorm injections

    NASA Astrophysics Data System (ADS)

    Gazey, N. G. J.; Lockwood, M.; Grande, M.; Perry, C. H.; Smith, P. N.; Coles, S.; Aylward, A. D.; Bunting, R. J.; Opgenoorth, H.; Wilken, B.

    1996-10-01

    We present combined observations made near midnight by the EISCAT radar, all-sky cameras and the combined released and radiation efects satellite (CRRES) shortly before and during a substorm. In particular, we study a discrete, equatorward-drifting auroral arc, seen several degrees poleward of the onset region. The arc passes through the field-aligned beam of the EISCAT radar and is seen to be associated with a considerable upflow of ionospheric plasma. During the substorm, the CRRES satellite observed two major injections, 17 min apart, the second of which was dominated by O+ ions. We show that the observed arc was in a suitable location in both latitude and MLT to have fed O+ ions into the second injection and that the upward flux of ions associated with it was sufficient to explain the observed injection. We interpret these data as showing that arcs in the nightside plasma-sheet boundary layer could be the source of O+ ions energised by a dipolarisation of the mid- and near-Earth tail, as opposed to ions ejected from the dayside ionosphere in the cleft ion fountain. Acknowledgements. We gratefully appreciate the on-line DMSP database facility at APL (Newell et al., 1991) from which this study has benefited greatly. We wish to thank E. Friis-Christensen for his encouragement and useful discussions. A. Y. would like to thank the Danish Meteorological Institute, where this work was done, for its hospitality during his stay there and the Nordic Baltic Scholarship Scheme for its financial support of this stay. Topical Editor K.-H. Glassmeier thanks M. J. Engebretson and H. Lühr for their help in evaluating this paper.--> Correspondence to: A. Yahnin-->

  16. Evaluating the Importance of Pickup Oxygen Ion Precipitation to the Martian Thermosphere

    NASA Astrophysics Data System (ADS)

    Fang, Xiaohua; Bougher, S.; Johnson, R.; Luhmann, J.

    2012-10-01

    Ionization of Martian neutral species and the subsequent pickup by the solar wind provides not only a non-thermal atmospheric loss process, but also a significant source to the thermospheric energy budget, depending on whether the ions ultimately leave or return to the planet. This study represents the first attempt to quantify the importance of returning energetic pickup ions to the Martian thermosphere on a global scale. To accomplish this, two global models are coupled: the Monte Carlo Pickup Ion Transport model (MCPIT) for evaluating particle precipitation at the exobase, and the Mars Thermosphere General Circulation Model (MTGCM) for the response in the upper atmosphere. Three cases are selected to explore the ion precipitation importance under nominal quiet, active, and extreme solar wind conditions at solar maximum, respectively. It is found that under quiet conditions, the particle input results in small but noticeable thermospheric temperature enhancement (by up to 8 K) at some place in the hemisphere that is opposite to the upstream convection electric field direction. In an active case in which the solar wind speed is as high as 1200 km/s with all the other parameters kept the same, the temperature is significantly enhanced by up to 14 K, which is large enough to be experimentally detected. We also examine the responses of the thermosphere to an extreme case, in which the impinging solar wind has greatly elevated dynamic pressure and magnetic field. In the extreme scenario, the thermosphere reacts dramatically: heating from pickup ion bombardment can totally overwhelm the solar EUV heating on the dayside, and the horizontal winds become much faster as well. It is suggested that precipitating pickup ions represent an important energy source to the Martian thermosphere and should be taken into account in global atmospheric modeling, particularly during disturbed solar wind conditions.

  17. Positron annihilation lifetime characterization of oxygen ion irradiated rutile TiO2

    NASA Astrophysics Data System (ADS)

    Luitel, Homnath; Sarkar, A.; Chakrabarti, Mahuya; Chattopadhyay, S.; Asokan, K.; Sanyal, D.

    2016-07-01

    Ferromagnetic ordering at room temperature has been induced in rutile phase of TiO2 polycrystalline sample by O ion irradiation. 96 MeV O ion induced defects in rutile TiO2 sample has been characterized by positron annihilation spectroscopic techniques. Positron annihilation results indicate the formation of cation vacancy (VTi, Ti vacancy) in these irradiated TiO2 samples. Ab initio density functional theoretical calculations indicate that in TiO2 magnetic moment can be induced either by creating Ti or O vacancies.

  18. Variation of the average 'freezing-in' temperature of oxygen ions with solar wind speed

    NASA Technical Reports Server (NTRS)

    Ogilvie, K. W.; Vogt, C.

    1980-01-01

    Observations of the average oxygen ionization equilibrium as a function of speed of the solar wind are presented. At low solar wind speeds they indicate a coronal temperature at the freezing-in point of (1.6 + or - 0.2) x 10 to the 6th K. At speeds above 450 km/sec the apparent temperature starts to rise rapidly. This rise is tentatively interpreted in terms of a lack of thermodynamic equilibrium in the source region.

  19. Influence of the residual oxygen in the plasma immersion ion implantation (PI3) processing of materials

    NASA Astrophysics Data System (ADS)

    Ueda, M.; Silva, A. R.; Mello, Carina B.; Silva, G.; Reuther, H.; Oliveira, V. S.

    2011-12-01

    In this work, we investigated the effects of the contaminants present in the vacuum chamber of the PI3 system, in particular, the residual oxygen, which results in the formation of the oxide compounds on the surface and hence is responsible for the high implantation energies required to achieve reasonably thick treated layers. We used a mass spectrometer (RGA) with a quadruple filter to verify the composition of the residual vacuum and pressure of the elements present in the chamber. Initially we found a high proportion of residual oxygen in a vacuum with a pressure of 1 × 10 -3 Pa. Minimizing the residual oxygen percentage in about 80%, by efficient cleaning of the chamber walls and by improving the gas feeding process, we mitigated the formation of oxides during the PI3 process. Therefore we achieved a highly efficient PI3 processing obtaining implanted layers reaching about 50 nm, even in cases such as an aluminum alloy, where is very difficult to nitrogen implant at low energies. We performed nitrogen PI3 treatment of SS304 and Al7075 using pulses of only 3 kV and 15 × 10 -6 s at 1 kHz with an operating pressure of 1 Pa.

  20. Molecular Adsorber Coating

    NASA Technical Reports Server (NTRS)

    Straka, Sharon; Peters, Wanda; Hasegawa, Mark; Hedgeland, Randy; Petro, John; Novo-Gradac, Kevin; Wong, Alfred; Triolo, Jack; Miller, Cory

    2011-01-01

    A document discusses a zeolite-based sprayable molecular adsorber coating that has been developed to alleviate the size and weight issues of current ceramic puck-based technology, while providing a configuration that more projects can use to protect against degradation from outgassed materials within a spacecraft, particularly contamination-sensitive instruments. This coating system demonstrates five times the adsorption capacity of previously developed adsorber coating slurries. The molecular adsorber formulation was developed and refined, and a procedure for spray application was developed. Samples were spray-coated and tested for capacity, thermal optical/radiative properties, coating adhesion, and thermal cycling. Work performed during this study indicates that the molecular adsorber formulation can be applied to aluminum, stainless steel, or other metal substrates that can accept silicate-based coatings. The coating can also function as a thermal- control coating. This adsorber will dramatically reduce the mass and volume restrictions, and is less expensive than the currently used molecular adsorber puck design.

  1. Electrical control of Co/Ni magnetism adjacent to gate oxides with low oxygen ion mobility

    SciTech Connect

    Yan, Y. N.; Zhou, X. J.; Li, F.; Cui, B.; Wang, Y. Y.; Wang, G. Y.; Pan, F.; Song, C.

    2015-09-21

    We investigate the electrical manipulation of Co/Ni magnetization through a combination of ionic liquid and oxide gating, where HfO{sub 2} with a low O{sup 2−} ion mobility is employed. A limited oxidation-reduction process at the metal/HfO{sub 2} interface can be induced by large electric field, which can greatly affect the saturated magnetization and Curie temperature of Co/Ni bilayer. Besides the oxidation/reduction process, first-principles calculations show that the variation of d electrons is also responsible for the magnetization variation. Our work discloses the role of gate oxides with a relatively low O{sup 2−} ion mobility in electrical control of magnetism, and might pave the way for the magneto-ionic memory with low power consumption and high endurance performance.

  2. Oxygen Ion--Conducting Ceramics: A New Application in High-Temperature--High-Pressure pH Sensors.

    PubMed

    Niedrach, L W

    1980-03-14

    Membrane electrodes fabricated from yttria-stabilized zirconia, a representative oxygen ion-conducting ceramic, show a linear voltage response to pH over the range 3 to 8 at 285 degrees C and a pressure of 1200 pounds per square inch (82 atmospheres). Test units have been operated continuously at 285 degrees C without failure for periods as long as 9 days. Unlike sensors which are based on electron transfer couples, such membrane electrodes are insensitive to changes in the oxidation-reduction environment and, in turn, exert no influence upon the environment. Such ceramic membranes can therefore be used for the direct measurement of the pH of geothermal brines, of water in nuclear reactors, and in high-temperature thermodynamic studies on aqueous systems.

  3. Collision integrals for the interaction of the ions of nitrogen and oxygen in a plasma at high temperatures and pressures

    NASA Technical Reports Server (NTRS)

    Stallcop, James R.; Partridge, Harry; Levin, E.

    1992-01-01

    The corrections to the transport cross-sections and collision integrals for Coulomb interactions arising from the application of realistic interaction energies of the ions of nitrogen and oxygen are investigated. Accurate potential-energy curves from an ab initio electronic-structure calculation and a semiclassical description of the scattering are used to determine the difference between the cross-sections for the real interaction forces and a Coulomb force for large values of the Debye shielding parameter. Graphs of the correction to the diffusion and viscosity-collision integrals are presented for temperatures from about 10,000 K to 150,000 K. This correction can be combined with tabulations of the collision integrals for shielded Coulomb potentials to determine the contribution of N(+)-N(+), N(+)-O(+), and O(+)-O(+) interactions to the transport properties of high-temperature air. Analytical forms are fitted to the calculated results to assist this application.

  4. Remarkable effect of the preparation technique on the state of cobalt ions in BEA zeolites evidenced by FTIR spectroscopy of adsorbed CO and NO, TPR and XRD.

    PubMed

    Mihaylova, Angelina; Hadjiivanov, Konstantin; Dzwigaj, Stanislaw; Che, Michel

    2006-10-01

    The state of cobalt in two BEA zeolites was studied by XRD, TPR, and FTIR spectroscopy using CO and NO as probe molecules. One of the samples, CoAlBEA (0.4 wt % of Co), was prepared by conventional ion exchange and the other, CoSiBEA (0.7 wt % Co), by a two-step postsynthesis method involving dealuminated SiBEA zeolite. The introduction of Co into SiBEA leads to an increase of unit cell parameters of the BEA structure and to the consumption of silanol groups in vacant T-sites of the dealuminated zeolite. In contrast, no structural changes are observed after incorporation of cobalt into AlBEA by ion-exchange. The reduction temperature of cobalt in CoSiBEA zeolite (1130 K), is much higher than for CoAlBEA and indicates a strong interaction of cobalt ions with SiBEA. Low-temperature CO adsorption on CoAlBEA results in (i) H-bonded CO, (ii) Co(3+)-CO adducts (2,208 cm(-1)) and (iii) a small amount of Co(2+)-CO complexes (2,188 cm(-1)). In agreement with these results, NO adsorption leads to the appearance of (i) NO(+) (2,133 cm(-1), formed with the participation of the zeolite acidic hydroxyls), (ii) Co(3+)-NO (1932 cm(-1)), and (iii) a small amount of Co(2+)(NO)(2) dinitrosyls (nu(s) = 1,898 and nu(as) = 1,814 cm(-1)). Low-temperature CO adsorption on CoSiBEA leads to formation of two kinds of Co(2+)-CO adducts (2,185 and 2,178 cm(-1)). No Co(3+) cations are detected. In line with these results, adsorption of NO reveals the existence of two kinds of Co(2+)(NO)(2) dinitrosyls (nu(s) = 1,888 and nu(as) = 1,808 cm(-1) and nu(s) = 1,878 and nu(as) = 1,799 cm(-1), respectively).

  5. Charge transfer during alkali-surface adsorbate collisions

    NASA Astrophysics Data System (ADS)

    Yang, Ye

    The study of charge transfer process between atomic particles and surface adsorbates is important, from both fundamental and practical points of view. Resonant charge transfer (RCT) process during the scattering of low-energy alkali ions from surfaces is proven to depend on the surface local electrostatic potential (LEP). This dissertation investigates the surface electronic environment around halogen and hydrogen adatoms on transition metal and silicon surfaces by using alkali ion scattering. Charge transfer in 7Li+ scattering from clean Si surfaces was shown to involve RCT between the Li 2s level and the Si dangling bonds. Hydrogen adsorption decreases the neutralization because it ties up the dangling bonds. The neutral fractions in 7Li + scattering from Cs/Si are also determined primarily by the dangling bond states, so that the surface LEP cannot be directly probed. Hydrogen adsorption on Cs/Si ties up the dangling bonds, thereby revealing the local potentials. The neutralization probabilities of Li+ backscattered from the hydrogen- and iodine-covered Ni(100) surface were measured. The neutral fraction does not change significantly on H-adsorbed surface. For iodine adsorption, however, unexpected high neutralization probabilities were found for Li scattered directly from iodine sites. Similar behavior were observed for Li+ scattering from I- and Br-covered Fe(100) and Fe(110). The neutralization of Li+ was measured as a function of the incident energy, adatom charge and coverage, and exit angle. It was found that the larger neutral fractions of Li scattered from the halogen sites are caused by a lower potential directly above the adatoms due to internal polarization. As the exit beam moves off-normal, the neutral fraction of Li scattered from iodine decreases. This is in contrast to Cs and Ag adsorbates where the neutral fractions increase for glancing exit trajectories. These angular-dependences are verified by a semi-quantitative theoretical analysis. To

  6. Dual-functional Memory and Threshold Resistive Switching Based on the Push-Pull Mechanism of Oxygen Ions

    PubMed Central

    Huang, Yi-Jen; Chao, Shih-Chun; Lien, Der-Hsien; Wen, Cheng-Yen; He, Jr-Hau; Lee, Si-Chen

    2016-01-01

    The combination of nonvolatile memory switching and volatile threshold switching functions of transition metal oxides in crossbar memory arrays is of great potential for replacing charge-based flash memory in very-large-scale integration. Here, we show that the resistive switching material structure, (amorphous TiOx)/(Ag nanoparticles)/(polycrystalline TiOx), fabricated on the textured-FTO substrate with ITO as the top electrode exhibits both the memory switching and threshold switching functions. When the device is used for resistive switching, it is forming-free for resistive memory applications with low operation voltage (<±1 V) and self-compliance to current up to 50 μA. When it is used for threshold switching, the low threshold current is beneficial for improving the device selectivity. The variation of oxygen distribution measured by energy dispersive X-ray spectroscopy and scanning transmission electron microscopy indicates the formation or rupture of conducting filaments in the device at different resistance states. It is therefore suggested that the push and pull actions of oxygen ions in the amorphous TiOx and polycrystalline TiOx films during the voltage sweep account for the memory switching and threshold switching properties in the device. PMID:27052322

  7. Dual-functional Memory and Threshold Resistive Switching Based on the Push-Pull Mechanism of Oxygen Ions.

    PubMed

    Huang, Yi-Jen; Chao, Shih-Chun; Lien, Der-Hsien; Wen, Cheng-Yen; He, Jr-Hau; Lee, Si-Chen

    2016-01-01

    The combination of nonvolatile memory switching and volatile threshold switching functions of transition metal oxides in crossbar memory arrays is of great potential for replacing charge-based flash memory in very-large-scale integration. Here, we show that the resistive switching material structure, (amorphous TiOx)/(Ag nanoparticles)/(polycrystalline TiOx), fabricated on the textured-FTO substrate with ITO as the top electrode exhibits both the memory switching and threshold switching functions. When the device is used for resistive switching, it is forming-free for resistive memory applications with low operation voltage (<± 1 V) and self-compliance to current up to 50 μA. When it is used for threshold switching, the low threshold current is beneficial for improving the device selectivity. The variation of oxygen distribution measured by energy dispersive X-ray spectroscopy and scanning transmission electron microscopy indicates the formation or rupture of conducting filaments in the device at different resistance states. It is therefore suggested that the push and pull actions of oxygen ions in the amorphous TiOx and polycrystalline TiOx films during the voltage sweep account for the memory switching and threshold switching properties in the device. PMID:27052322

  8. Dual-functional Memory and Threshold Resistive Switching Based on the Push-Pull Mechanism of Oxygen Ions

    NASA Astrophysics Data System (ADS)

    Huang, Yi-Jen; Chao, Shih-Chun; Lien, Der-Hsien; Wen, Cheng-Yen; He-Hau, Jr.; Lee, Si-Chen

    2016-04-01

    The combination of nonvolatile memory switching and volatile threshold switching functions of transition metal oxides in crossbar memory arrays is of great potential for replacing charge-based flash memory in very-large-scale integration. Here, we show that the resistive switching material structure, (amorphous TiOx)/(Ag nanoparticles)/(polycrystalline TiOx), fabricated on the textured-FTO substrate with ITO as the top electrode exhibits both the memory switching and threshold switching functions. When the device is used for resistive switching, it is forming-free for resistive memory applications with low operation voltage (<±1 V) and self-compliance to current up to 50 μA. When it is used for threshold switching, the low threshold current is beneficial for improving the device selectivity. The variation of oxygen distribution measured by energy dispersive X-ray spectroscopy and scanning transmission electron microscopy indicates the formation or rupture of conducting filaments in the device at different resistance states. It is therefore suggested that the push and pull actions of oxygen ions in the amorphous TiOx and polycrystalline TiOx films during the voltage sweep account for the memory switching and threshold switching properties in the device.

  9. Using specialized adsorbents for remediation

    SciTech Connect

    Hochmuth, D.P.; Grant, A.

    1995-11-01

    This paper describes two remediation case studies in which specialized adsorbents were used. In one case, the adsorbents were used to treat effluent from a soil vapor extraction system. In the other case, the adsorbents were used to treat air from a groundwater air stripper. The specialized adsorbents effectively removed volatile organic compounds from each air stream.

  10. Double differential distribution of electron emission in the ionization of water molecules by fast bare oxygen ions

    NASA Astrophysics Data System (ADS)

    Bhattacharjee, Shamik; Biswas, Shubhadeep; Bagdia, Chandan; Roychowdhury, Madhusree; Nandi, Saikat; Misra, Deepankar; Monti, J. M.; Tachino, C. A.; Rivarola, R. D.; Champion, C.; Tribedi, Lokesh C.

    2016-03-01

    The doubly differential distributions of low-energy electron emission in the ionization of water molecules under the impact of fast bare oxygen ions with energy of 48 MeV are measured. The measured data are compared with two quantum-mechanical models, i.e. the post and prior versions of the continuum distorted wave-eikonal initial state (CDW-EIS) approximation, and the first-order Born approximation with initial and final wavefunctions verifying correct boundary conditions (CB1). An overall excellent qualitative agreement is found between the data and the CDW-EIS models whereas the CB1 model showed substantial deviation. However, the detailed angular distributions display some discrepancies with both CDW-EIS models. The single differential and total cross-sections exhibit good agreement with the CDW-EIS models. The present detailed data set could also be used as an input for modeling highly charged ion induced radiation damage in living tissues, whose most abundant component is water. Similar measurements are also carried out for a projectile energy of 60 MeV. However, since the double differential cross-section data show similar results the details are not provided here, except for the total ionization cross-sections results.

  11. A mixed proton, oxygen ion, and electron conducting cathode for SOFCs based on oxide proton conductors

    NASA Astrophysics Data System (ADS)

    Yang, Lei; Liu, Ze; Wang, Shizhong; Choi, YongMan; Zuo, Chendong; Liu, Meilin

    A composite cathode, consisting of Ba(Zr 0.1Ce 0.7Y 0.2)O 3- δ (BZCY) and La 0.6Sr 0.4Co 0.2Fe 0.8O 3- δ (LSCF), has shown high catalytic activity toward oxygen reduction, demonstrating a peak power density of 855 mW cm -2 at 750 °C. The chemical compatibility between BZCY and LSCF is excellent since there was no evidence of chemical reaction between the two after being fired at 1100 °C for 10 h. The stability of the composite cathode is further shown in single cells operated at 750 and 600 °C for 100 h without observable degradation in performance.

  12. Measurement of Atomic Oxygen in Diffuse Aurora and Ion Density in the E-Region

    NASA Technical Reports Server (NTRS)

    Sharp, William E.

    1997-01-01

    An ion mass spectrometer (IMS) was refurbished, calibrated and supplied to the University of Colorado payload (Dr. Charles Barth, P.I.) which was launched from White Sands in September of 1993 as NASA 33.062. The nose cone failed to deploy and their were problems with the ACS so the mission was declared a failure. However, the door covering the IMS deployed and the instrument obtained data. The launch occurred shortly after a payload carrying solar x-ray detectors was launched. Thus a small portion of the Colorado payload science was salvaged; namely, the NO(+)/O2(+) ratio to compare with the measured x-ray flux. Figure I shows the NO(+) to O2(+) ratio vs. altitude. The behavior is typical of the E-region.

  13. Gas storage using fullerene based adsorbents

    NASA Technical Reports Server (NTRS)

    Loutfy, Raouf O. (Inventor); Lu, Xiao-Chun (Inventor); Li, Weijiong (Inventor); Mikhael, Michael G. (Inventor)

    2000-01-01

    This invention is directed to the synthesis of high bulk density high gas absorption capacity adsorbents for gas storage applications. Specifically, this invention is concerned with novel gas absorbents with high gravimetric and volumetric gas adsorption capacities which are made from fullerene-based materials. By pressing fullerene powder into pellet form using a conventional press, then polymerizing it by subjecting the fullerene to high temperature and high inert gas pressure, the resulting fullerene-based materials have high bulk densities and high gas adsorption capacities. By pre-chemical modification or post-polymerization activation processes, the gas adsorption capacities of the fullerene-based adsorbents can be further enhanced. These materials are suitable for low pressure gas storage applications, such as oxygen storage for home oxygen therapy uses or on-board vehicle natural gas storage. They are also suitable for storing gases and vapors such as hydrogen, nitrogen, carbon dioxide, and water vapor.

  14. Regenerative adsorbent heat pump

    NASA Technical Reports Server (NTRS)

    Jones, Jack A. (Inventor)

    1991-01-01

    A regenerative adsorbent heat pump process and system is provided which can regenerate a high percentage of the sensible heat of the system and at least a portion of the heat of adsorption. A series of at least four compressors containing an adsorbent is provided. A large amount of heat is transferred from compressor to compressor so that heat is regenerated. The process and system are useful for air conditioning rooms, providing room heat in the winter or for hot water heating throughout the year, and, in general, for pumping heat from a lower temperature to a higher temperature.

  15. New force field parameters for metalloproteins I: Divalent copper ion centers including three histidine residues and an oxygen-ligated amino acid residue.

    PubMed

    Wise, Olivia; Coskuner, Orkid

    2014-06-30

    Transition metal ion complexation with proteins is ubiquitous across such diverse fields as neurodegenerative and cardiovascular diseases and cancer. In this study, the structures of divalent copper ion centers including three histidine and one oxygen-ligated amino acid residues and the relative binding affinities of the oxygen-ligated amino acid residues with these metal ion centers, which are debated in the literature, are presented. Furthermore, new force field parameters, which are currently lacking for the full-length metal-ligand moieties, are developed for metalloproteins that have these centers. These new force field parameters enable investigations of metalloproteins possessing these binding sites using molecular simulations. In addition, the impact of using the atom equivalence and inequivalence atomic partial charge calculation procedures on the simulated structures of these metallopeptides, including hydration properties, is described.

  16. Contrasting hydrological processes of meteoric water incursion during magmatic-hydrothermal ore deposition: An oxygen isotope study by ion microprobe

    NASA Astrophysics Data System (ADS)

    Fekete, Szandra; Weis, Philipp; Driesner, Thomas; Bouvier, Anne-Sophie; Baumgartner, Lukas; Heinrich, Christoph A.

    2016-10-01

    Meteoric water convection has long been recognized as an efficient means to cool magmatic intrusions in the Earth's upper crust. This interplay between magmatic and hydrothermal activity thus exerts a primary control on the structure and evolution of volcanic, geothermal and ore-forming systems. Incursion of meteoric water into magmatic-hydrothermal systems has been linked to tin ore deposition in granitic plutons. In contrast, evidence from porphyry copper ore deposits suggests that crystallizing subvolcanic magma bodies are only affected by meteoric water incursion in peripheral zones and during late post-ore stages. We apply high-resolution secondary ion mass spectrometry (SIMS) to analyze oxygen isotope ratios of individual growth zones in vein quartz crystals, imaged by cathodo-luminescence microscopy (SEM-CL). Existing microthermometric information from fluid inclusions enables calculation of the oxygen isotope composition of the fluid from which the quartz precipitated, constraining the relative timing of meteoric water input into these two different settings. Our results confirm that incursion of meteoric water directly contributes to cooling of shallow granitic plutons and plays a key role in concurrent tin mineralization. By contrast, data from two porphyry copper deposits suggest that downward circulating meteoric water is counteracted by up-flowing hot magmatic fluids. Our data show that porphyry copper ore deposition occurs close to a magmatic-meteoric water interface, rather than in a purely magmatic fluid plume, confirming recent hydrological modeling. On a larger scale, the expulsion of magmatic fluids against the meteoric water interface can shield plutons from rapid convective cooling, which may aid the build-up of large magma chambers required for porphyry copper ore formation.

  17. Adsorbent and adsorbent bed for materials capture and separation processes

    SciTech Connect

    Liu, Wei

    2011-01-25

    A method device and material for performing adsorption wherein a fluid mixture is passed through a channel in a structured adsorbent bed having a solid adsorbent comprised of adsorbent particles having a general diameter less than 100 um, loaded in a porous support matrix defining at least one straight flow channel. The adsorbent bed is configured to allow passage of a fluid through said channel and diffusion of a target material into said adsorbent under a pressure gradient driving force. The targeted molecular species in the fluid mixture diffuses across the porous support retaining layer, contacts the adsorbent, and adsorbs on the adsorbent, while the remaining species in the fluid mixture flows out of the channel.

  18. High-resolution X-ray study of the multiple ionization of Pd atoms by fast oxygen ions

    NASA Astrophysics Data System (ADS)

    Czarnota, M.; Banaś, D.; Berset, M.; Chmielewska, D.; Dousse, J.-Cl.; Hoszowska, J.; Maillard, Y.-P.; Mauron, O.; Pajek, M.; Polasik, M.; Raboud, P. A.; Rzadkiewicz, J.; Słabkowska, K.; Sujkowski, Z.

    2010-04-01

    The multiple ionization of the L- and M-shells of Pd by fast oxygen ions has been studied by measuring with high-resolution the satellite structures of the Lα1,2 X-ray transitions. Relativistic multi-configuration Dirac-Fock (MCDF) calculations were used to interpret the complex X-ray spectrum, allowing to derive the number of L- and M-shell spectator vacancies at the moment of the X-ray emission. After correcting these numbers for the atomic vacancy rearrangement processes that take place prior to the X-ray emission, the ionization probabilities corresponding to the collision time were obtained. The latter were compared to predictions of the semiclassical approximation (SCA) and the geometrical model. The SCA calculations were performed using relativistic hydrogenic and self-consistent Dirac-Hartree-Fock (DHF) electronic wave functions. It was found that the use of the more realistic DHF wave functions in the SCA calculations leads to a much better description of the measured ionization probabilities for both the L- and M-shells.

  19. Designing nitrogen-enriched echinus-like carbon capsules for highly efficient oxygen reduction reaction and lithium ion storage.

    PubMed

    Hu, Chuangang; Wang, Lixia; Zhao, Yang; Ye, Minhui; Chen, Qing; Feng, Zhihai; Qu, Liangti

    2014-07-21

    Both structural and compositional modulations are important for high-performance electrode materials in energy conversion/storage devices. Here hierarchical-structure nitrogen-rich hybrid porous carbon capsules with bamboo-like carbon nanotube whiskers (N-CC@CNTs) grown in situ have been specifically designed, which combine the advantageous features of high surface area, abundant active sites, easy access to medium and favorable mass transport. As a result, the newly prepared N-CC@CNTs show highly efficient catalytic activity in oxygen reduction reaction in alkaline media for fuel cells, which not only outperforms commercial Pt-based catalysts in terms of kinetic limiting current, stability and tolerance to methanol crossover effect, but is also better than most of the nanostructured carbon-based catalysts reported previously. On the other hand, as an anode material for lithium ion batteries, the N-CC@CNTs obtained also exhibit an excellent reversible capacity of ca. 1337 mA h g(-1) at 0.5 A g(-1), outstanding rate capability and long cycling stability, even at a current density of 20 A g(-1). The capacity is the highest among all the heteroatom-doped carbon materials reported so far, and is even higher than that of many of the composites of metal, metal oxides or metal sulfides with carbon materials. PMID:24906180

  20. Designing nitrogen-enriched echinus-like carbon capsules for highly efficient oxygen reduction reaction and lithium ion storage.

    PubMed

    Hu, Chuangang; Wang, Lixia; Zhao, Yang; Ye, Minhui; Chen, Qing; Feng, Zhihai; Qu, Liangti

    2014-07-21

    Both structural and compositional modulations are important for high-performance electrode materials in energy conversion/storage devices. Here hierarchical-structure nitrogen-rich hybrid porous carbon capsules with bamboo-like carbon nanotube whiskers (N-CC@CNTs) grown in situ have been specifically designed, which combine the advantageous features of high surface area, abundant active sites, easy access to medium and favorable mass transport. As a result, the newly prepared N-CC@CNTs show highly efficient catalytic activity in oxygen reduction reaction in alkaline media for fuel cells, which not only outperforms commercial Pt-based catalysts in terms of kinetic limiting current, stability and tolerance to methanol crossover effect, but is also better than most of the nanostructured carbon-based catalysts reported previously. On the other hand, as an anode material for lithium ion batteries, the N-CC@CNTs obtained also exhibit an excellent reversible capacity of ca. 1337 mA h g(-1) at 0.5 A g(-1), outstanding rate capability and long cycling stability, even at a current density of 20 A g(-1). The capacity is the highest among all the heteroatom-doped carbon materials reported so far, and is even higher than that of many of the composites of metal, metal oxides or metal sulfides with carbon materials.

  1. Effects of Carbon Structure and Surface Oxygen on the Carbon's Performance as the Anode in Lithium-Ion Battery Determined

    NASA Technical Reports Server (NTRS)

    Hung, Ching-Cheh

    2000-01-01

    Four carbon materials (C1, C2, C3, and C4) were tested electrochemically at the NASA Glenn Research Center at Lewis Field to determine their performance in lithium-ion batteries. They were formed as shown in the figure. This process caused very little carbon loss. Products C1 and C3 contained very little oxygen because of the final overnight heating at 540 C. Products C2 and C4, on the other hand, contained small amounts of basic oxide. The electrochemical test involved cycles of lithium intercalation and deintercalation using C/saturated LiI-50/50 (vol %) ethylene carbonate (EC) and dimethyl carbonate (DMC)/Li half cell. The cycling test, which is summarized in the table, resulted in three major conclusions. The capacity of the carbon with a basic oxide surface converges to a constant 1. value quickly (within 4 cycles), possibly because the oxide prevents solvent from entering the carbon structure and, therefore, prolongs the carbon s cycle life. Under certain conditions, the disordered carbon can store more lithium than its 2. precursor. These samples and their precursor can intercalate at 200 mA/g and deintercalate at 3. a rate of 2000 mA/g without significant capacity loss.

  2. Facile preparation of porous Co3O4 nanosheets for high-performance lithium ion batteries and oxygen evolution reaction

    NASA Astrophysics Data System (ADS)

    Li, Zhangpeng; Yu, Xin-Yao; Paik, Ungyu

    2016-04-01

    Two dimensional (2D) porous nanostructures are of great interest due to their high surface area and rich edge sites, which are favorable for a wide variety of applications. In this communication, well-defined porous Co3O4 nanosheets (PCNSs) are successfully fabricated using graphene oxide as sacrificial template. The 2D structure and porous nature effectively provide more exposed active sites for electrochemical reaction and facilitate easier ion transportation across the sheets. As a result, the as-prepared PCNSs exhibit remarkable lithium storage performance, showing high reversible capacity of 1380 mAh g-1 even after 240 discharge/charge cycles at a current density of 500 mA g-1 and good rate capability (606 mAh g-1 at 10 A g-1). Moreover, it also shows a good electrocatalytic activity for the electrochemical oxygen evolution reaction with an overpotential of 368 mV for driving the current density of 10 mA cm-2 in 1 M KOH and a small Tafel slope of 59 mV dec-1.

  3. Ultrafiltration by a compacted clay membrane. I - Oxygen and hydrogen isotopic fractionation. II - Sodium ion exclusion at various ionic strengths.

    NASA Technical Reports Server (NTRS)

    Coplen, T. B.; Hanshaw, B. B.

    1973-01-01

    Laboratory experiments were carried out to determine the magnitude of the isotopic fractionation of distilled water and of 0.01N NaCl forced to flow at ambient temperature under a hydraulic pressure drop of 100 bars across a montmorillonite disk compacted to a porosity of 35% by a pressure of 330 bars. The ultrafiltrates in both experiments were depleted in D by 2.5% and in O-18 by 0.8% relative to the residual solution. No additional isotopic fractionation due to a salt-filtering mechanism was observed at NaCl concentrations up to 0.01N. Adsorption is most likely the principal mechanism which produces isotopic fractionation, but molecular diffusion may play a minor role. The results suggest that oxygen and hydrogen isotopic fractionation of ground water during passage through compacted clayey sediments should be a common occurrence, in accord with published interpretations of isotopic data from the Illinois and Alberta basins. It is shown how it is possible to proceed from the ion exchange capacity of clay minerals and, by means of the Donnan membrane equilibrium concept and the Teorell-Meyer-Siever theory, develop a theory to explain why and to what extent ultrafiltration occurs when solutions of known concentration are forced to flow through a clay membrane.

  4. Redox-inactive metal ions modulate the reactivity and oxygen release of mononuclear non-haem iron(III)-peroxo complexes.

    PubMed

    Bang, Suhee; Lee, Yong-Min; Hong, Seungwoo; Cho, Kyung-Bin; Nishida, Yusuke; Seo, Mi Sook; Sarangi, Ritimukta; Fukuzumi, Shunichi; Nam, Wonwoo

    2014-10-01

    Redox-inactive metal ions that function as Lewis acids play pivotal roles in modulating the reactivity of oxygen-containing metal complexes and metalloenzymes, such as the oxygen-evolving complex in photosystem II and its small-molecule mimics. Here we report the synthesis and characterization of non-haem iron(III)-peroxo complexes that bind redox-inactive metal ions, (TMC)Fe(III)-(μ,η(2):η(2)-O2)-M(n+) (M(n+) = Sr(2+), Ca(2+), Zn(2+), Lu(3+), Y(3+) and Sc(3+); TMC, 1,4,8,11-tetramethyl-1,4,8,11-tetraazacyclotetradecane). We demonstrate that the Ca(2+) and Sr(2+) complexes showed similar electrochemical properties and reactivities in one-electron oxidation or reduction reactions. However, the properties and reactivities of complexes formed with stronger Lewis acidities were found to be markedly different. Complexes that contain Ca(2+) or Sr(2+) ions were oxidized by an electron acceptor to release O2, whereas the release of O2 did not occur for complexes that bind stronger Lewis acids. We discuss these results in the light of the functional role of the Ca(2+) ion in the oxidation of water to dioxygen by the oxygen-evolving complex.

  5. Redox-inactive metal ions modulate the reactivity and oxygen release of mononuclear non-haem iron(III)-peroxo complexes

    NASA Astrophysics Data System (ADS)

    Bang, Suhee; Lee, Yong-Min; Hong, Seungwoo; Cho, Kyung-Bin; Nishida, Yusuke; Seo, Mi Sook; Sarangi, Ritimukta; Fukuzumi, Shunichi; Nam, Wonwoo

    2014-10-01

    Redox-inactive metal ions that function as Lewis acids play pivotal roles in modulating the reactivity of oxygen-containing metal complexes and metalloenzymes, such as the oxygen-evolving complex in photosystem II and its small-molecule mimics. Here we report the synthesis and characterization of non-haem iron(III)-peroxo complexes that bind redox-inactive metal ions, (TMC)FeIII-(μ,η2:η2-O2)-Mn+ (Mn+ = Sr2+, Ca2+, Zn2+, Lu3+, Y3+ and Sc3+; TMC, 1,4,8,11-tetramethyl-1,4,8,11-tetraazacyclotetradecane). We demonstrate that the Ca2+ and Sr2+ complexes showed similar electrochemical properties and reactivities in one-electron oxidation or reduction reactions. However, the properties and reactivities of complexes formed with stronger Lewis acidities were found to be markedly different. Complexes that contain Ca2+ or Sr2+ ions were oxidized by an electron acceptor to release O2, whereas the release of O2 did not occur for complexes that bind stronger Lewis acids. We discuss these results in the light of the functional role of the Ca2+ ion in the oxidation of water to dioxygen by the oxygen-evolving complex.

  6. Redox-inactive metal ions modulate the reactivity and oxygen release of mononuclear non-haem iron(III)–peroxo complexes

    DOE PAGES

    Bang, Suhee; Lee, Yong -Min; Hong, Seungwoo; Cho, Kyung -Bin; Nishida, Yusuke; Seo, Mi Sook; Sarangi, Ritimukta; Fukuzumi, Shunichi; Nam, Wonwoo

    2014-09-14

    Redox-inactive metal ions that function as Lewis acids play pivotal roles in modulating the reactivity of oxygen-containing metal complexes and metalloenzymes, such as the oxygen-evolving complex in photosystem II and its small-molecule mimics. Here we report the synthesis and characterization of non-haem iron(III)–peroxo complexes that bind redox-inactive metal ions, (TMC)FeIII–(μ,η2:η2-O2)–Mn+ (Mn+ = Sr2+, Ca2+, Zn2+, Lu3+, Y3+ and Sc3+; TMC, 1,4,8,11-tetramethyl-1,4,8,11-tetraazacyclotetradecane). We demonstrate that the Ca2+ and Sr2+ complexes showed similar electrochemical properties and reactivities in one-electron oxidation or reduction reactions. However, the properties and reactivities of complexes formed with stronger Lewis acidities were found to be markedly different. Inmore » conclusion, complexes that contain Ca2+ or Sr2+ ions were oxidized by an electron acceptor to release O2, whereas the release of O2 did not occur for complexes that bind stronger Lewis acids. Furthermore, we discuss these results in the light of the functional role of the Ca2+ ion in the oxidation of water to dioxygen by the oxygen-evolving complex.« less

  7. Effects of vacuum annealing and oxygen ion beam bombarding on the electrical and optical properties of ITO films deposited by E-beam evaporation

    NASA Astrophysics Data System (ADS)

    Pan, Yongqiang; Hang, Lingxia

    2012-10-01

    Tin doped indium oxide (ITO) transparent conductive thin films with composition of 10 wt% SnO2 and 89.8 wt% In2O3 have been deposited by electron beam evaporation technique on K9 glass substrates at room temperature. The post annealing processes are done in vacuum with different annealing temperature at 100, 200, 300 and 350 ° for 1 hour, respectively. The oxygen ion energy is 800 eV; oxygen ion beam bombarding time is 10,20,30,40 and 50min, respectively. The results show that conductivity of ITO thin films are improved by increasing annealing temperature. The resistivity of the ITO thin films decrease from 5.2×10-3Ω •cm at room temperature to 1.3×10-3Ω •cm(350 °C). The transmittance values of all samples in the visible range have been increased. As the oxygen ion beam bombarding time increases the resistivity reduce from 5.2×10-3Ω •cm to 9×10-4Ω •cm, the transmittance value improve from 66% to 82% at 550nm. Finally, the vacuum annealing and oxygen ion beam bombarding are done simultaneously, at temperature of 350 °C for 1 hours, ion bombardment time for 40 min. The resistivity of obtained ITO thin film is 7×10-4Ω •cm. The maximum transmittance value is above 89% in the visible wavelength region.

  8. Determination and speciation of trace and ultratrace selenium ions by energy-dispersive X-ray fluorescence spectrometry using graphene as solid adsorbent in dispersive micro-solid phase extraction.

    PubMed

    Kocot, Karina; Leardi, Riccardo; Walczak, Beata; Sitko, Rafal

    2015-03-01

    A dispersive micro-solid phase extraction (DMSPE) with graphene as a solid adsorbent and ammonium pyrrolidinedithiocarbamate (APDC) as a chelating agent was proposed for speciation and detemination of inorganic selenium by the energy-dispersive X-ray fluorescence spectrometry (EDXRF). In developed DMSPE, graphene particles are dispersed throughout the analyzed solution, therefore reaction between Se(IV)-APDC complexes and graphene nanoparticles occurs immediately. The concentration of Se(VI) is calculated as the difference between the concentration of selenite after and before prereduction of selenate. A central composite face-centered design with 3 center points was performed in order to optimize conditions and to study the effect of four variables (pH of the sample, concentration of APDC, concentration of Triton-X-100, and sample volume). The best results were obtained when suspension consisting of 200 µg of graphene nanosheets, 1.2 mg of APDC and 0.06 mg of Triton-X-100 was rapidly injected to the 50 mL of the analyzed solution. Under optimized conditions Se ions can be determined with a very good recovery (97.7±5.0% and 99.2±6.6% for Se(IV) and Se(VI), respectively) and precision (RSD=5.1-6.6%). Proposed DMSPE/EDXRF procedure allowed to obtain low detection limits (0.032 ng mL(-1)) and high enrichment factor (1013±15). The proposed methodology was successfully applied for the determination of Se in mineral, tap, lake and sea water samples as well as in biological materials (Lobster Hepatopancreas and Pig Kidney).

  9. Determination and speciation of trace and ultratrace selenium ions by energy-dispersive X-ray fluorescence spectrometry using graphene as solid adsorbent in dispersive micro-solid phase extraction.

    PubMed

    Kocot, Karina; Leardi, Riccardo; Walczak, Beata; Sitko, Rafal

    2015-03-01

    A dispersive micro-solid phase extraction (DMSPE) with graphene as a solid adsorbent and ammonium pyrrolidinedithiocarbamate (APDC) as a chelating agent was proposed for speciation and detemination of inorganic selenium by the energy-dispersive X-ray fluorescence spectrometry (EDXRF). In developed DMSPE, graphene particles are dispersed throughout the analyzed solution, therefore reaction between Se(IV)-APDC complexes and graphene nanoparticles occurs immediately. The concentration of Se(VI) is calculated as the difference between the concentration of selenite after and before prereduction of selenate. A central composite face-centered design with 3 center points was performed in order to optimize conditions and to study the effect of four variables (pH of the sample, concentration of APDC, concentration of Triton-X-100, and sample volume). The best results were obtained when suspension consisting of 200 µg of graphene nanosheets, 1.2 mg of APDC and 0.06 mg of Triton-X-100 was rapidly injected to the 50 mL of the analyzed solution. Under optimized conditions Se ions can be determined with a very good recovery (97.7±5.0% and 99.2±6.6% for Se(IV) and Se(VI), respectively) and precision (RSD=5.1-6.6%). Proposed DMSPE/EDXRF procedure allowed to obtain low detection limits (0.032 ng mL(-1)) and high enrichment factor (1013±15). The proposed methodology was successfully applied for the determination of Se in mineral, tap, lake and sea water samples as well as in biological materials (Lobster Hepatopancreas and Pig Kidney). PMID:25618680

  10. Inorganic chemically active adsorbents (ICAAs)

    SciTech Connect

    Ally, M.R.; Tavlarides, L.

    1997-10-01

    Oak Ridge National Laboratory (ORNL) researchers are developing a technology that combines metal chelation extraction technology and synthesis chemistry. They begin with a ceramic substrate such as alumina, titanium oxide or silica gel because they provide high surface area, high mechanical strength, and radiolytic stability. One preparation method involves silylation to hydrophobize the surface, followed by chemisorption of a suitable chelation agent using vapor deposition. Another route attaches newly designed chelating agents through covalent bonding by the use of coupling agents. These approaches provide stable and selective, inorganic chemically active adsorbents (ICAAs) tailored for removal of metals. The technology has the following advantages over ion exchange: (1) higher mechanical strength, (2) higher resistance to radiation fields, (3) higher selectivity for the desired metal ion, (4) no cation exchange, (5) reduced or no interference from accompanying anions, (6) faster kinetics, and (7) easy and selective regeneration. Target waste streams include metal-containing groundwater/process wastewater at ORNL`s Y-12 Plant (multiple metals), Savannah River Site (SRS), Rocky Flats (multiple metals), and Hanford; aqueous mixed wastes at Idaho National Engineering Laboratory (INEL); and scrubber water generated at SRS and INEL. Focus Areas that will benefit from this research include Mixed Waste, and Subsurface Contaminants.

  11. Characteristics of ring current protons and oxygen ions during the 7 January 2015 and 17 March 2015 storms: Van Allen Probes/RBSPICE observations

    NASA Astrophysics Data System (ADS)

    Keika, K.; Seki, K.; Nose, M.; Machida, S.; Miyoshi, Y.; Lanzerotti, L. J.; Mitchell, D. G.; Gkioulidou, M.; Gerrard, A. J.; Manweiler, J. W.

    2015-12-01

    We investigate enhancements and losses of energetic (~50-~500 keV) protons and oxygen ions during two intense storms on January 7 and March 17 in 2015. We use proton and oxygen ion data from RBSPICE onboard Van Allen Probes. During the January 7 storm (Dstmin = -99 nT), Van Allen Probes explored the inner magnetosphere on the night side, with both spacecraft located around midnight at apogee. Their orbits were in opposite phase. RBSPICE data are available from both spacecraft during the rapid recovery of the storm. We analyze energy spectra of both species to identify whether the ring current is symmetric or not, and determine the dominant loss process. During the March 17 storm (Dstmin = -223 nT), Van Allen Probes traveled in the pre-midnight sector during the outbound paths and around midnight during the inbound path. The orbits of the two spacecraft were in opposite phase. The Dst index during the storm showed a two-step decrease with the first minimum at 9 UT and the second at 22 UT. Enhancements of ring current ions began at RBSPICE-B at ~7 UT, and RBSPICE-A entered the ring current region at ~9 UT. The RBSPICE data show penetration of energetic protons (μ~0.1 keV/nT) down to L~4 during the first storm development. Protons penetrated more deeply (as low as L~3) during the second enhancement. The protons, which we confirmed made a dominant contribution to energy density at L = 3-4, are more enhanced in flux around the storm maximum. The flux of 200-400 keV oxygen ions was enhanced and localized around midnight near the end of the first storm development. Oxygen ion enhancements during the second development were seen in a wide range of MLT (pre-midnight to midnight). We examine the evolution of ion energy spectra to identify whether each phase of the multi-step storm development was due to deep penetration of transport/injections, density enhancements, or/and non-adiabatic acceleration of protons and oxygen ions.

  12. Chemical State of Surface Oxygen on Carbon and Its Effects on the Capacity of the Carbon Anode in a Lithium-Ion Battery Investigated

    NASA Technical Reports Server (NTRS)

    Hung, Ching-Cheh

    2001-01-01

    In a lithium-ion battery, the lithium-storage capacity of the carbon anode is greatly affected by a surface layer formed during the first half cycle of lithium insertion and release into and out of the carbon anode. The formation of this solid-electrolyte interface, in turn, is affected by the chemistry of the carbon surface. A study at the NASA Glenn Research Center examined the cause-and-effect relations. Information obtained from this research could contribute in designing a high-capacity lithium-ion battery and, therefore, small, powerful spacecraft. In one test, three types of surfaces were examined: (1) a surface with low oxygen content (1.5 at.%) and a high concentration of active sites, (2) a surface with 4.5 at.% -OH or -OC type oxygen, and (3) a surface with 6.5 at.% O=C type oxygen. The samples were made from the same precursor and had similar bulk properties. They were tested under a constant current of 10 mA/g in half cells that used lithium metal as the counter electrode and 0.5 M lithium iodide in 50/50 (vol%) ethylene carbonate and dimethyl carbonate as the electrolyte. For the first cycle of the electrochemical test, the graph describes the voltage of the carbon anode versus the lithium metal as a function of the capacity (amount of lithium insertion or release). From these data, it can be observed that the surface with low oxygen and a high concentration of active sites could result in a high irreversible capacity. Such a high irreversible capacity could be prevented if the active sites were allowed to react with oxygen in air, producing -OH or -OC type oxygen. The O=C type oxygen, on the other hand, could greatly reduce the capacity of lithium intercalation and, therefore, needs to be avoided during battery fabrication.

  13. A Reliable Hybrid Adsorbent for Efficient Radioactive Cesium Accumulation from Contaminated Wastewater

    NASA Astrophysics Data System (ADS)

    Awual, Md. Rabiul; Yaita, Tsuyoshi; Miyazaki, Yuji; Matsumura, Daiju; Shiwaku, Hideaki; Taguchi, Tomitsugu

    2016-01-01

    Cesium (Cs) removal from nuclear liquid wastewater has become an emerging issue for safeguarding public health after the accident at the Fukushima Daiichi Nuclear Power Plant. A novel macrocyclic ligand of o-benzo-p-xylyl-22-crown-6-ether (OBPX22C6) was developed and successfully immobilized onto mesoporous silica for the preparation of hybrid adsorbent. The benzene ring π electron is the part of crown ether of OBPX22C6 for easy orientation of the macrocyclic compound for making the π electron donation with Cs complexation. The potential and feasibility of the hybrid adsorbent as being Cs selective was evaluated in terms of sensitivity, selectivity and reusability. The results clarified that the Cs removal process was rapid and reached saturation within a short time. Considering the effect of competitive ions, sodium (Na) did not markedly affect the Cs adsorption whereas potassium (K) was slightly affected due to the similar ionic radii. However, the oxygen in long ethylene glycol chain in OBPX22C6 was expected to show strong coordination, including Cs-π interaction with Cs even in the presence of the high amount of K and Na. Due to its high selectivity and reusability, significant volume reduction is expected as this promising hybrid adsorbent is used for Cs removal in Fukushima wastewater.

  14. A Reliable Hybrid Adsorbent for Efficient Radioactive Cesium Accumulation from Contaminated Wastewater.

    PubMed

    Awual, Md Rabiul; Yaita, Tsuyoshi; Miyazaki, Yuji; Matsumura, Daiju; Shiwaku, Hideaki; Taguchi, Tomitsugu

    2016-01-28

    Cesium (Cs) removal from nuclear liquid wastewater has become an emerging issue for safeguarding public health after the accident at the Fukushima Daiichi Nuclear Power Plant. A novel macrocyclic ligand of o-benzo-p-xylyl-22-crown-6-ether (OBPX22C6) was developed and successfully immobilized onto mesoporous silica for the preparation of hybrid adsorbent. The benzene ring π electron is the part of crown ether of OBPX22C6 for easy orientation of the macrocyclic compound for making the π electron donation with Cs complexation. The potential and feasibility of the hybrid adsorbent as being Cs selective was evaluated in terms of sensitivity, selectivity and reusability. The results clarified that the Cs removal process was rapid and reached saturation within a short time. Considering the effect of competitive ions, sodium (Na) did not markedly affect the Cs adsorption whereas potassium (K) was slightly affected due to the similar ionic radii. However, the oxygen in long ethylene glycol chain in OBPX22C6 was expected to show strong coordination, including Cs-π interaction with Cs even in the presence of the high amount of K and Na. Due to its high selectivity and reusability, significant volume reduction is expected as this promising hybrid adsorbent is used for Cs removal in Fukushima wastewater.

  15. A Reliable Hybrid Adsorbent for Efficient Radioactive Cesium Accumulation from Contaminated Wastewater

    PubMed Central

    Awual, Md. Rabiul; Yaita, Tsuyoshi; Miyazaki, Yuji; Matsumura, Daiju; Shiwaku, Hideaki; Taguchi, Tomitsugu

    2016-01-01

    Cesium (Cs) removal from nuclear liquid wastewater has become an emerging issue for safeguarding public health after the accident at the Fukushima Daiichi Nuclear Power Plant. A novel macrocyclic ligand of o-benzo-p-xylyl-22-crown-6-ether (OBPX22C6) was developed and successfully immobilized onto mesoporous silica for the preparation of hybrid adsorbent. The benzene ring π electron is the part of crown ether of OBPX22C6 for easy orientation of the macrocyclic compound for making the π electron donation with Cs complexation. The potential and feasibility of the hybrid adsorbent as being Cs selective was evaluated in terms of sensitivity, selectivity and reusability. The results clarified that the Cs removal process was rapid and reached saturation within a short time. Considering the effect of competitive ions, sodium (Na) did not markedly affect the Cs adsorption whereas potassium (K) was slightly affected due to the similar ionic radii. However, the oxygen in long ethylene glycol chain in OBPX22C6 was expected to show strong coordination, including Cs-π interaction with Cs even in the presence of the high amount of K and Na. Due to its high selectivity and reusability, significant volume reduction is expected as this promising hybrid adsorbent is used for Cs removal in Fukushima wastewater. PMID:26818070

  16. A Reliable Hybrid Adsorbent for Efficient Radioactive Cesium Accumulation from Contaminated Wastewater.

    PubMed

    Awual, Md Rabiul; Yaita, Tsuyoshi; Miyazaki, Yuji; Matsumura, Daiju; Shiwaku, Hideaki; Taguchi, Tomitsugu

    2016-01-01

    Cesium (Cs) removal from nuclear liquid wastewater has become an emerging issue for safeguarding public health after the accident at the Fukushima Daiichi Nuclear Power Plant. A novel macrocyclic ligand of o-benzo-p-xylyl-22-crown-6-ether (OBPX22C6) was developed and successfully immobilized onto mesoporous silica for the preparation of hybrid adsorbent. The benzene ring π electron is the part of crown ether of OBPX22C6 for easy orientation of the macrocyclic compound for making the π electron donation with Cs complexation. The potential and feasibility of the hybrid adsorbent as being Cs selective was evaluated in terms of sensitivity, selectivity and reusability. The results clarified that the Cs removal process was rapid and reached saturation within a short time. Considering the effect of competitive ions, sodium (Na) did not markedly affect the Cs adsorption whereas potassium (K) was slightly affected due to the similar ionic radii. However, the oxygen in long ethylene glycol chain in OBPX22C6 was expected to show strong coordination, including Cs-π interaction with Cs even in the presence of the high amount of K and Na. Due to its high selectivity and reusability, significant volume reduction is expected as this promising hybrid adsorbent is used for Cs removal in Fukushima wastewater. PMID:26818070

  17. Slags in a Large Variation Range of Oxygen Potential Based on the Ion and Molecule Coexistence Theory

    NASA Astrophysics Data System (ADS)

    Yang, Xue-Min; Li, Jin-Yan; Zhang, Meng; Chai, Guo-Min; Zhang, Jian

    2014-12-01

    A thermodynamic model for predicting sulfide capacity of CaO-FeO-Fe2O3-Al2O3-P2O5 slags in a large variation range of oxygen potential corresponding to mass percentage of FetO from 1.88 to 55.50 pct, i.e., IMCT- model, has been developed by coupling with the deduced desulfurization mechanism of the slags based on the ion and molecule coexistence theory (IMCT). The developed IMCT- model has been verified through comparing the determined sulfide capacity after Ban-ya et al.[20] with the calculated by the developed IMCT- model and the calculated by the reported sulfide capacity models such as the KTH model. Mass percentage of FetO as 6.75 pct corresponding to the mass action concentration of FetO as 0.0637 or oxygen partial as 2.27 × 10-6 Pa is the criterion for distinguishing reducing and oxidizing zones for the slags. Sulfide capacity of the slags in reducing zone is controlled by reaction ability of CaO regardless of slag oxidization ability. However, sulfide capacity of the slags in oxidizing zone shows an obvious increase tendency with the increasing of slag oxidization ability. Sulfide capacity of the slags in reducing zone keeps almost constant with variation of the simplified complex basicity (pct CaO)/((pct Al2O3) + (pct P2O5)), or optical basicity, or the mass action concentration ratios of N FeO/ N CaO, , , and . Sulfide capacity of the slags in oxidizing zone shows an obvious increase with the increasing of the simplified complex basicity (pct CaO)/((pct Al2O3) + (pct P2O5)) or optical basicity, or the aforementioned mass action concentration ratios. Thus, the aforementioned mass action concentration ratios and the corresponding mass percentage ratios of various iron oxides to basic oxide CaO are recommended to represent the comprehensive effect of various iron oxides and basic oxide CaO on sulfide capacity of the slags.

  18. Copper ions strongly activate the phosphoinositide-3-kinase/Akt pathway independent of the generation of reactive oxygen species.

    PubMed

    Ostrakhovitch, Elena A; Lordnejad, Mohammad Reza; Schliess, Freimut; Sies, Helmut; Klotz, Lars-Oliver

    2002-01-15

    Copper is implicated in metabolic disorders, such as Wilson's disease or Alzheimer's disease. Analysis of signaling pathways regulating cellular survival and function in response to a copper stress is crucial for understanding the pathogenesis of such diseases. Exposure of human skin fibroblasts or HeLa cells to Cu(2+) resulted in a dose- and time-dependent activation of the antiapoptotic kinase Akt/protein kinase B, starting at concentrations as low as 3 microM. Only Cu(II), but not Cu(I), had this effect. Activation of Akt was accompanied by phosphorylation of a downstream target of Akt, glycogen synthase kinase-3. Inhibitors of phosphoinositide-3-kinase (PI3K) completely blocked activation of Akt by Cu(2+), indicating a requirement of PI3K for Cu(2+)-induced activation of Akt. Indeed, cellular PI3K activity was strongly enhanced after exposure to Cu(2+). Copper ions may lead to the formation of reactive oxygen species, such as hydrogen peroxide. Activation of Akt by hydrogen peroxide or growth factors is known to proceed via the activation growth factor receptors. In line with this, pretreatment with inhibitors of growth factor receptor tyrosine kinases blocked activation of Akt by hydrogen peroxide and growth factors, as did a src-family tyrosine kinase inhibitor or the broad-spectrum tyrosine kinase inhibitor genistein. Activation of Akt by Cu(2+), however, remained unimpaired, implying (i) that tyrosine kinase activation is not involved in Cu(2+) activation of Akt and (ii) that activation of the PI3K/Akt pathway by Cu(2+) is initiated independently of that induced by reactive oxygen species. Comparison of the time course of the oxidation of 2',7'-dichlorodihydrofluorescein in copper-treated cells with that of Akt activation led to the conclusion that production of hydroperoxides cannot be an upstream event in copper-induced Akt activation. Rather, both activation of Akt and generation of ROS are proposed to occur in parallel, regulating cell survival after a

  19. Optical waveguide properties of Ca0.4Ba0.6Nb2O6 crystal formed by oxygen ion irradiation

    NASA Astrophysics Data System (ADS)

    Wang, Tie-Jun; Zhou, Yu-Fan; Yu, Xiao-Fei; Liu, Tao; Zhang, Lian; Song, Hong-Lian; Qiao, Mei; Wang, Xue-Lin

    2015-07-01

    We report the fabrication of a planar optical waveguide in a Ca0.4Ba0.6Nb2O6 crystal by irradiation with 6.0 MeV oxygen ions. We measured the guiding mode by the prism-coupling method at 633 nm and 1539 nm. The near-field intensity distributions were measured by the end-face coupling setup at a wavelength of 633 nm. The reflectivity calculation method (RCM) was used for reconstructing refractive index profiles. SRIM was used to simulate the electronic and nuclear stopping power caused by oxygen ion irradiation, and the finite-difference beam propagation method (FD-BPM) was used to simulate the near-field intensity distributions. Micro-Raman spectra were measured at room temperature in air to study the differences between the substrate and waveguide region.

  20. Oil palm biomass as an adsorbent for heavy metals.

    PubMed

    Vakili, Mohammadtaghi; Rafatullah, Mohd; Ibrahim, Mahamad Hakimi; Abdullah, Ahmad Zuhairi; Salamatinia, Babak; Gholami, Zahra

    2014-01-01

    Many industries discharge untreated wastewater into the environment. Heavy metals from many industrial processes end up as hazardous pollutants of wastewaters.Heavy metal pollution has increased in recent decades and there is a growing concern for the public health risk they may pose. To remove heavy metal ions from polluted waste streams, adsorption processes are among the most common and effective treatment methods. The adsorbents that are used to remove heavy metal ions from aqueous media have both advantages and disadvantages. Cost and effectiveness are two of the most prominent criteria for choosing adsorbents. Because cost is so important, great effort has been extended to study and find effective lower cost adsorbents.One class of adsorbents that is gaining considerable attention is agricultural wastes. Among many alternatives, palm oil biomasses have shown promise as effective adsorbents for removing heavy metals from wastewater. The palm oil industry has rapidly expanded in recent years, and a large amount of palm oil biomass is available. This biomass is a low-cost agricultural waste that exhibits, either in its raw form or after being processed, the potential for eliminating heavy metal ions from wastewater. In this article, we provide background information on oil palm biomass and describe studies that indicate its potential as an alternative adsorbent for removing heavy metal ions from wastewater. From having reviewed the cogent literature on this topic we are encouraged that low-cost oil-palm-related adsorbents have already demonstrated outstanding removal capabilities for various pollutants.Because cost is so important to those who choose to clean waste streams by using adsorbents, the use of cheap sources of unconventional adsorbents is increasingly being investigated. An adsorbent is considered to be inexpensive when it is readily available, is environmentally friendly, is cost-effective and be effectively used in economical processes. The

  1. Oil palm biomass as an adsorbent for heavy metals.

    PubMed

    Vakili, Mohammadtaghi; Rafatullah, Mohd; Ibrahim, Mahamad Hakimi; Abdullah, Ahmad Zuhairi; Salamatinia, Babak; Gholami, Zahra

    2014-01-01

    Many industries discharge untreated wastewater into the environment. Heavy metals from many industrial processes end up as hazardous pollutants of wastewaters.Heavy metal pollution has increased in recent decades and there is a growing concern for the public health risk they may pose. To remove heavy metal ions from polluted waste streams, adsorption processes are among the most common and effective treatment methods. The adsorbents that are used to remove heavy metal ions from aqueous media have both advantages and disadvantages. Cost and effectiveness are two of the most prominent criteria for choosing adsorbents. Because cost is so important, great effort has been extended to study and find effective lower cost adsorbents.One class of adsorbents that is gaining considerable attention is agricultural wastes. Among many alternatives, palm oil biomasses have shown promise as effective adsorbents for removing heavy metals from wastewater. The palm oil industry has rapidly expanded in recent years, and a large amount of palm oil biomass is available. This biomass is a low-cost agricultural waste that exhibits, either in its raw form or after being processed, the potential for eliminating heavy metal ions from wastewater. In this article, we provide background information on oil palm biomass and describe studies that indicate its potential as an alternative adsorbent for removing heavy metal ions from wastewater. From having reviewed the cogent literature on this topic we are encouraged that low-cost oil-palm-related adsorbents have already demonstrated outstanding removal capabilities for various pollutants.Because cost is so important to those who choose to clean waste streams by using adsorbents, the use of cheap sources of unconventional adsorbents is increasingly being investigated. An adsorbent is considered to be inexpensive when it is readily available, is environmentally friendly, is cost-effective and be effectively used in economical processes. The

  2. Designing nitrogen-enriched echinus-like carbon capsules for highly efficient oxygen reduction reaction and lithium ion storage

    NASA Astrophysics Data System (ADS)

    Hu, Chuangang; Wang, Lixia; Zhao, Yang; Ye, Minhui; Chen, Qing; Feng, Zhihai; Qu, Liangti

    2014-06-01

    Both structural and compositional modulations are important for high-performance electrode materials in energy conversion/storage devices. Here hierarchical-structure nitrogen-rich hybrid porous carbon capsules with bamboo-like carbon nanotube whiskers (N-CC@CNTs) grown in situ have been specifically designed, which combine the advantageous features of high surface area, abundant active sites, easy access to medium and favorable mass transport. As a result, the newly prepared N-CC@CNTs show highly efficient catalytic activity in oxygen reduction reaction in alkaline media for fuel cells, which not only outperforms commercial Pt-based catalysts in terms of kinetic limiting current, stability and tolerance to methanol crossover effect, but is also better than most of the nanostructured carbon-based catalysts reported previously. On the other hand, as an anode material for lithium ion batteries, the N-CC@CNTs obtained also exhibit an excellent reversible capacity of ca. 1337 mA h g-1 at 0.5 A g-1, outstanding rate capability and long cycling stability, even at a current density of 20 A g-1. The capacity is the highest among all the heteroatom-doped carbon materials reported so far, and is even higher than that of many of the composites of metal, metal oxides or metal sulfides with carbon materials.Both structural and compositional modulations are important for high-performance electrode materials in energy conversion/storage devices. Here hierarchical-structure nitrogen-rich hybrid porous carbon capsules with bamboo-like carbon nanotube whiskers (N-CC@CNTs) grown in situ have been specifically designed, which combine the advantageous features of high surface area, abundant active sites, easy access to medium and favorable mass transport. As a result, the newly prepared N-CC@CNTs show highly efficient catalytic activity in oxygen reduction reaction in alkaline media for fuel cells, which not only outperforms commercial Pt-based catalysts in terms of kinetic limiting

  3. Oxygen depth profiling by resonant backscattering and glow discharge optical emission spectroscopy of Ti-6Al-4V alloy oxidized by ion implantation and plasma based treatment

    NASA Astrophysics Data System (ADS)

    Nsengiyumva, S.; Topic, M.; Pichon, L.; Comrie, C. M.; Mtshali, C.

    2016-10-01

    Oxygen depth profiling by means of 16O(α,α)16O backscattering and glow discharge optical emission spectroscopy (GDOES) was investigated in two different sets of Ti-6Al-4V samples. The first set was made of Ti-6Al-4V samples implanted at room temperature and 550 °C with 50 and 150 keV O+ ions at fluences ranging from 1.5 × 1017 to 6.0 × 1017 ions/cm2. The second set consisted of Ti-6Al-4V samples treated at 550 °C for 7 h and 24 h under low pressure (8 Pa) oxygen, eventually with RF plasma activation. These results are part of a wider investigation on Ti-6Al-4V motivated by recent publications which have shown that an oxide layer can enhance hydrogen absorption and can then promote Ti-6Al-4V alloys as efficient hydrogen storage materials. The results obtained by the two characterization techniques were compared and discussed, enabling to adjust the dependence to the oxygen concentration of the sputtering rates to be used in the time-to-depth transformation required in GDOES analysis. Considering the low thickness of oxidized alloy, usual procedures employed in GDOES depth calculation were indeed not adapted. Once calibrated thanks to the resonant RBS, GDOES can then be easily employed as fast characterization of oxidized and/or hydrogenated surface of Ti-6Al-4V. The obtained results show that the oxygen content into the surface oxidized layer slightly increases in samples implanted at higher fluence and higher temperature. However the overall oxidized layer thickness (<200 nm) remains within the projected ion depth range and is not significantly increased by thermal diffusion at 550 °C. Taken into account the initial oxide layer, the incorporated oxygen quantity mainly corresponds to the implanted fluence but it can be slightly higher with 550 °C implantation, indicating a slight additional oxidation by residual oxygen or surface contamination. The oxygen penetrations and contents in samples oxidized by thermally activated diffusion treatments were more

  4. Joint contributions of Ag ions and oxygen vacancies to conducting filament evolution of Ag/TaO{sub x}/Pt memory device

    SciTech Connect

    Chung, Yu-Lung; Cheng, Wen-Hui; Chen, Wei-Chih; Jhan, Sheng-An; Chen, Jen-Sue; Jeng, Jiann-Shing

    2014-10-28

    The electroforming and resistive switching behaviors in the Ag/TaO{sub x}/Pt trilayer structure are investigated under a continual change of temperatures between 300 K and 100 K to distinguish the contributions of Ag ions and oxygen vacancies in developing of conducting filaments. For either electroforming or resistive switching, a significantly higher forming/set voltages is needed as the device is operated at 100 K, as compared to that observed when operating at 300 K. The disparity in forming/set voltages of Ag/TaO{sub x}/Pt operating at 300 K and 100 K is attributed to the contribution of oxygen vacancies, in addition to Ag atoms, in formation of conducting filament at 100 K since the mobilities of oxygen vacancies and Ag ions become comparable at low temperature. The presence of oxygen vacancy segment in the conducting filament also modifies the reset current from a gradually descending behavior (at 300 K) to a sharp drop (at 100 K). Furthermore, the characteristic set voltage and reset current are irreversible as the operation temperature is brought from 100 K back to 300 K, indicating the critical role of filament constituents on the switching behaviors of Ag/oxide/Pt system.

  5. In situ calcium mapping in the mouse retina via time-of-flight secondary ion mass spectrometry: modulation of retinal angiogenesis by calcium ion in development and oxygen-induced retinopathy.

    PubMed

    Kim, Jeong Hun; Kim, Jin Hyoung; Yu, Young Suk; Kim, Dong Hun; Lee, Tae Geol; Moon, Dae Won; Kim, Kyu-Won

    2008-10-01

    Pathological angiogenesis in the eye is the most common cause of blindness in all age groups. In physiological and pathological cellular processes including angiogenesis, ion homeostasis is greatly affected. This study is to investigate the role of calcium ion in physiological and pathological angiogenesis in the retina, which is based on the results of ion mapping by time-of-flight secondary ion mass spectrometry (TOF-SIMS). We provided that calcium distribution is the most accordant to change with physiological vessel formation of development in the retina and pathological angiogenesis of oxygen-induced retinopathy (OIR), which is supported by ion mapping in retinal tissue using TOF-SIMS. In addition to anti-proliferative and anti-angiogenic activity of the calcium inhibitor on endothelial cells, retinal neovascularization of OIR was effectively inhibited by the calcium inhibitor. Calcium ion could play a crucial role in physiological and pathological angiogenesis in the retina. Moreover, TOF-SIMS could be a good method to simultaneously evaluate the changes of variable ions of the retina in biological processes.

  6. Gold nanoparticle-aluminum oxide adsorbent for efficient removal of mercury species from natural waters.

    PubMed

    Lo, Sut-I; Chen, Po-Cheng; Huang, Chih-Ching; Chang, Huan-Tsung

    2012-03-01

    We report a new adsorbent for removal of mercury species. By mixing Au nanoparticles (NPs) 13 nm in diameter with aluminum oxide (Al(2)O(3)) particles 50-200 μm in diameter, Au NP-Al(2)O(3) adsorbents are easily prepared. Three adsorbents, Al(2)O(3), Au NPs, and Au NP-Al(2)O(3), were tested for removal of mercury species [Hg(2+), methylmercury (MeHg(+)), ethylmercury (EtHg(+)), and phenylmercury (PhHg(+))]. The Au NP adsorbent has a higher binding affinity (dissociation constant; K(d) = 0.3 nM) for Hg(2+) ions than the Al(2)O(3) adsorbent (K(d) = 52.9 nM). The Au NP-Al(2)O(3) adsorbent has a higher affinity for mercury species and other tested metal ions than the Al(2)O(3) and Au NP adsorbents. The Au NP-Al(2)O(3) adsorbent provides a synergic effect and, thus, is effective for removal of most tested metal ions and organic mercury species. After preconcentration of mercury ions by an Au NP-Al(2)O(3) adsorbent, analysis of mercury ions down to the subppq level in aqueous solution was performed by inductively coupled plasma mass spectrometry (ICP-MS). The Au NP-Al(2)O(3) adsorbent allows effective removal of mercury species spiked in lake water, groundwater, and seawater with efficiencies greater than 97%. We also used Al(2)O(3) and Au NP-Al(2)O(3) adsorbents sequentially for selectively removing Hg(2+) and MeHg(+) ions from water. The low-cost, effective, and stable Au NP-Al(2)O(3) adsorbent shows great potential for economical removal of various mercury species.

  7. The influence of negative ions in helium-oxygen barrier discharges: II. 1D fluid simulation and adaption to the experiment

    NASA Astrophysics Data System (ADS)

    Nemschokmichal, Sebastian; Tschiersch, Robert; Meichsner, Jürgen

    2016-10-01

    A 1D fluid simulation was developed to investigate the influence of negative ions in a helium-oxygen barrier discharge between two glass plates at a distance of 3~\\text{mm} . The paper describes setting up the simulation for a pressure of 500~\\text{mbar} and an admixture of 400~\\text{ppm} oxygen to helium. In order to enable the comparison with laser photodetachment experiments, the simulation is adapted to the experimentally observed discharge current and gap voltage by varying gas temperature, flux of thermally desorpted electrons and secondary electron emission coefficients. The discharge is characterized by evaluation of the most important elementary collision processes as well as the kinetics of the charged species. Besides, the influence of long-living species on the discharge behavior is taken into account by long-time simulations. The negative ions are characterized by their spatio-temporal distribution in the gap and their production and loss processes. The comparison between simulations without and with consideration of negative ions reveals the importance of negative ions on the discharge development.

  8. The effect of oxygen on segregation-induced redistribution of rare-earth elements in silicon layers amorphized by ion implantation

    SciTech Connect

    Aleksandrov, O. V.

    2006-08-15

    A model of segregation-induced redistribution of impurities of rare-earth elements during solid-phase epitaxial crystallization of silicon layers amorphized by ion implantation is developed. This model is based on the assumption that a transition layer with a high mobility of atoms is formed at the interphase boundary on the side of a-Si; the thickness of this layer is governed by the diffusion length of vacancies in a-Si. The Er concentration profiles in Si implanted with both erbium and oxygen ions are analyzed in the context of the model. It shown that, in the case of high doses of implantation of rare-earth ions, it is necessary to take into account the formation of R{sub m} clusters (m = 4), where R denotes the atom of a rare-earth element, whereas, if oxygen ions are also implanted, formation of the complexes RO{sub n} (n = 3-6) should be taken into account; these complexes affect the transition-layer thickness and segregation coefficient.

  9. Metal ion effect on the switch of mechanism from direct oxygen transfer to metal ion-coupled electron transfer in the sulfoxidation of thioanisoles by a non-heme iron(IV)-oxo complex.

    PubMed

    Park, Jiyun; Morimoto, Yuma; Lee, Yong-Min; Nam, Wonwoo; Fukuzumi, Shunichi

    2011-04-13

    The mechanism of sulfoxidation of thioaniosoles by a non-heme iron(IV)-oxo complex is switched from direct oxygen transfer to metal ion-coupled electron transfer by the presence of Sc(3+). The switch in the sulfoxidation mechanism is dependent on the one-electron oxidation potentials of thioanisoles. The rate of sulfoxidation is accelerated as much as 10(2)-fold by the addition of Sc(3+).

  10. Low-loss planar and stripe waveguides in Nd{sup 3+}-doped silicate glass produced by oxygen-ion implantation

    SciTech Connect

    Wang, Lei; Chen, Feng; Wang, Xue-Lin; Wang, Ke-Ming; Jiao, Yang; Wang, Liang-Ling; Li, Xi-Shan; Lu, Qing-Ming; Ma, Hong-Ji; Nie, Rui

    2007-03-01

    We report on the fabrication and characterization of low-loss planar and stripe waveguides in a Nd{sup 3+}-doped glass by 6 MeV oxygen-ion implantation at a dose of 1x10{sup 15} ions/cm{sup 2}. The dark mode spectroscopy of the planar waveguide was measured using a prism coupling arrangement. The refractive index profile of the planar waveguide was reconstructed from a code based on the reflectivity calculation method. The results indicate that a refractive index enhanced region as well as an optical barrier have been created after the ion beam processing. The near-field mode profiles of the stripe waveguide were obtained by an end-fire coupling arrangement, by which three quasitransverse electric modes were observed. After annealing, the propagation losses of the planar and stripe waveguides were reduced to be {approx}0.5 and {approx}1.8 dB/cm, respectively.

  11. Sensitivity enhancement of carbon nanotube based ammonium ion sensors through surface modification by using oxygen plasma treatment

    SciTech Connect

    Yeo, Sanghak; Woong Jang, Chi; Lee, Seok; Min Jhon, Young; Choi, Changrok

    2013-02-18

    We have shown that the sensitivity of carbon nanotube (CNT) based sensors can be enhanced as high as 74 times through surface modification by using the inductively coupled plasma chemical vapor deposition method with oxygen. The plasma treatment power was maintained as low as 10 W within 20 s, and the oxygen plasma was generated far away from the sensors to minimize the plasma damage. From X-ray photoelectron spectroscopy analysis, we found that the concentration of oxygen increased with the plasma treatment time, which implies that oxygen functional groups or defect sites were generated on the CNT surface.

  12. Redox-inactive metal ions modulate the reactivity and oxygen release of mononuclear non-haem iron(III)–peroxo complexes

    SciTech Connect

    Bang, Suhee; Lee, Yong -Min; Hong, Seungwoo; Cho, Kyung -Bin; Nishida, Yusuke; Seo, Mi Sook; Sarangi, Ritimukta; Fukuzumi, Shunichi; Nam, Wonwoo

    2014-09-14

    Redox-inactive metal ions that function as Lewis acids play pivotal roles in modulating the reactivity of oxygen-containing metal complexes and metalloenzymes, such as the oxygen-evolving complex in photosystem II and its small-molecule mimics. Here we report the synthesis and characterization of non-haem iron(III)–peroxo complexes that bind redox-inactive metal ions, (TMC)FeIII–(μ,η22-O2)–Mn+ (Mn+ = Sr2+, Ca2+, Zn2+, Lu3+, Y3+ and Sc3+; TMC, 1,4,8,11-tetramethyl-1,4,8,11-tetraazacyclotetradecane). We demonstrate that the Ca2+ and Sr2+ complexes showed similar electrochemical properties and reactivities in one-electron oxidation or reduction reactions. However, the properties and reactivities of complexes formed with stronger Lewis acidities were found to be markedly different. In conclusion, complexes that contain Ca2+ or Sr2+ ions were oxidized by an electron acceptor to release O2, whereas the release of O2 did not occur for complexes that bind stronger Lewis acids. Furthermore, we discuss these results in the light of the functional role of the Ca2+ ion in the oxidation of water to dioxygen by the oxygen-evolving complex.

  13. Removal and recycle of phosphate from treated water of sewage plants with zirconium ferrite adsorbent by high gradient magnetic separation

    NASA Astrophysics Data System (ADS)

    Ito, D.; Nishimura, K.; Miura, O.

    2009-03-01

    Zirconium ferrite particles are good adsorbent for phosphate ions. Magnetic separation characteristics for removal of phosphate from treated water of sewage plants with the adsorbent have been studied to prevent eutrophication of semi-enclosed bay, e.g. the bay of Tokyo. Based on the adsorption for the phosphate ions and ferromagnetic properties of the zirconium ferrite adsorbent, high gradient magnetic separation characteristics with using superconducting magnet was discussed. Very rapid magnetic filtration velocity, i.e. 1m/s, and regeneration properties of the adsorbent indicate that the zirconium ferrite is the excellent adsorbent for phosphorus removal and recycle from treated water of large scale sewage plants.

  14. A novel isotope analysis of oxygen in uranium oxides: comparison of secondary ion mass spectrometry, glow discharge mass spectrometry and thermal ionization mass spectrometry

    NASA Astrophysics Data System (ADS)

    Pajo, L.; Tamborini, G.; Rasmussen, G.; Mayer, K.; Koch, L.

    2001-05-01

    The natural variation of the oxygen isotopic composition is used among geologists to determine paleotemperatures and the origin of minerals. In recent studies, oxygen isotopic composition has been recognized as a possible tool for identification of the origin of seized uranium oxides in nuclear forensic science. In the last 10 years, great effort has been made to develop new direct and accurate n( 18O)/ n( 16O) measurements methods. Traditionally, n( 18O)/ n( 16O) analyses are performed by gas mass spectrometry. In this work, a novel oxygen isotope analysis by thermal ionization mass spectrometry (TIMS), using metal oxide ion species (UO +), is compared to the direct methods: glow discharge mass spectrometry (GDMS) and secondary ion mass spectrometry (SIMS). Because of the possible application of the n( 18O)/ n( 16O) ratio in nuclear forensics science, the samples were solid, pure UO 2 or U 3O 8 particles. The precision achieved using TIMS analysis was 0.04%, which is similar or even better than the one obtained using the SIMS technique (0.05%), and clearly better if compared to that of GDMS (0.5%). The samples used by TIMS are micrograms in size. The suitability of TIMS as a n( 18O)/ n( 16O) measurement method is verified by SIMS measurements. In addition, TIMS results have been confirmed by characterizing the n( 18O)/ n( 16O) ratio of UO 2 sample also by the traditional method of static vacuum mass spectrometry at the University of Chicago.

  15. Improvements of anti-corrosion and mechanical properties of NiTi orthopedic materials by acetylene, nitrogen and oxygen plasma immersion ion implantation

    NASA Astrophysics Data System (ADS)

    Poon, Ray W. Y.; Ho, Joan P. Y.; Liu, Xuanyong; Chung, C. Y.; Chu, Paul K.; Yeung, Kelvin W. K.; Lu, William W.; Cheung, Kenneth M. C.

    2005-08-01

    Nickel-titanium shape memory alloys (NiTi) are useful materials in orthopedics and orthodontics due to their unique super-elasticity and shape memory effects. However, the problem associated with the release of harmful Ni ions to human tissues and fluids has been raising safety concern. Hence, it is necessary to produce a surface barrier to impede the out-diffusion of Ni ions from the materials. We have conducted acetylene, nitrogen and oxygen plasma immersion ion implantation (PIII) into NiTi alloys in an attempt to improve the surface properties. All the implanted and annealed samples surfaces exhibit outstanding corrosion and Ni out-diffusion resistance. Besides, the implanted layers are mechanically stronger than the substrate underneath. XPS analyses disclose that the layer formed by C2H2 PIII is composed of mainly TiCx with increasing Ti to C concentration ratios towards the bulk. The nitrogen PIII layer is observed to be TiN, whereas the oxygen PIII layer is composed of oxides of Ti4+, Ti3+ and Ti2+.

  16. Gold recovery from low concentrations using nanoporous silica adsorbent

    NASA Astrophysics Data System (ADS)

    Aledresse, Adil

    The development of high capacity adsorbents with uniform porosity denoted 5%MP-HMS (5% Mercaptopropyl-Hexagonal Mesoporous Structure) to extract gold from noncyanide solutions is presented. The preliminary studies from laboratory simulated noncyanide gold solutions show that the adsorption capacities of these materials are among the highest reported. The high adsorption saturation level of these materials, up to 1.9 mmol/g (37% of the adsorbent weight) from gold chloride solutions (potassium tetrachloroaurate) and 2.9 mmol/g (57% of the adsorbent weight) from gold bromide solutions (potassium tetrabromoaurate) at pH = 2, is a noteworthy feature of these materials. This gold loading from [AuC4]- and [AuBr4 ]- solutions corresponds to a relative Au:S molar ratio of 2.5:1 and 3.8:1, respectively. These rates are significantly higher than the usual 1:1 (Au:S) ratio expected for metal ion binding with the material. The additional gold ions loaded have been spontaneously reduced to metallic gold in the mesoporous material. Experimental studies indicated high maximum adsorptions of gold as high as 99.9% recovery. Another promising attribute of these materials is their favourable adsorption kinetics. The MP-HMS reaches equilibrium (saturation) in less than 1 minute of exposure in gold bromide and less than 10 minutes in gold chloride. The MP-HMS materials adsorption is significantly improved by agitation and the adsorption capacity of Au (III) ions increases with the decrease in pH. The recovery of adsorbed gold and the regeneration of spent adsorbent were investigated for MP-HMS adsorbent. The regenerated adsorbent (MP-HMS) maintained its adsorption capacity even after repeated use and all the gold was successfully recovered from the spent adsorbent. For the fist time, a promising adsorbent system has been found that is capable of effectively concentrating gold thiosulphate complexes, whereas conventional carbon-inpulp (CIP) and carbon-in-leach (CIL) systems fail. The

  17. Oxygen safety

    MedlinePlus

    COPD - oxygen safety; Chronic obstructive pulmonary disease - oxygen safety; Chronic obstructive airways disease - oxygen safety; Emphysema - oxygen safety; Heart failure - oxygen-safety; Palliative care - oxygen safety; ...

  18. A kinetic model of the formation of the hot oxygen geocorona 2. Influence of O{sup +} ion precipitation

    SciTech Connect

    Bisikalo, D.V.; Shematovich, V.I.; Gerard, J.C.

    1995-03-01

    The authors model oxygen precipitation in the upper atmosphere by a Monte Carlo treatment of the Boltzman equation, during geomagnetically unstable times. They attempt to simulate the O precipitation for the storm conditions on September 17, 1971. They find that O precipitation greatly modifies the electron velocity distribution for the bulk oxygen population in the upper atmosphere, resulting in an enhanced hot O tail density.

  19. K-, L- and M-shell X-ray productions induced by oxygen ions in the 0.8-1.6 MeV/amu range

    NASA Astrophysics Data System (ADS)

    Gorlachev, I.; Gluchshenko, N.; Ivanov, I.; Kireyev, A.; Kozin, S.; Kurakhmedov, A.; Platov, A.; Zdorovets, M.

    2016-08-01

    The X-ray production cross sections induced by oxygen ions with projectile energies from 12.8 to 25.6 MeV for the elements from Al to Bi were measured. The applied approach is based on calculation of X-ray production cross sections through the cross section of Rutherford backscattering, which can be calculated with high accuracy using the Rutherford formula. The experimental results are compared to the predictions of ECPSSR and PWBA theories calculated with the ISICS code.

  20. Observation of internal structure of the L-shell x-ray hypersatellites for palladium atoms multiply ionized by fast oxygen ions

    SciTech Connect

    Czarnota, M.; Banas, D.; Pajek, M.; Berset, M.; Dousse, J.-Cl.; Hoszowska, J.; Maillard, Y.-P.; Mauron, O.; Raboud, P. A.; Chmielewska, D.; Rzadkiewicz, J.; Sujkowski, Z.; Polasik, M.; Slabkowska, K.

    2010-06-15

    An observation of the internal structure of the L-shell hypersatellite x rays resulting from the one-photon decay of L{sup -2} double-vacancy states in palladium multiply ionized by oxygen ions is reported. The Pd L{sub 3}{yields}M{sub 4,5} x-ray spectrum was measured with a von Hamos high-resolution crystal spectrometer. The complex shape of the observed spectrum could be interpreted in detail using relativistic multiconfiguration Dirac-Fock calculations. The relative intensities of the measured x rays were found to be in good agreement with semiclassical approximation calculations using relativistic Dirac-Hartree-Fock wave functions.

  1. The effect of 100 MeV oxygen ion on electrical and optical properties of nonlinear optical l-alanine sodium nitrate single crystals

    SciTech Connect

    Ahlam, M. A.; Prakash, A. P. Gnana

    2012-06-05

    Single crystals of nonlinear optical (NLO) L-alanine Sodium Nitrate (LASN) were grown by slow evaporation method. The grown crystals were irradiated by 100 MeV oxygen ions with the cumulative doses of 1Mrad, 6 Mrad and 10 Mrad. The dielectric properties, differential scanning calorimetry (DSC) and second harmonic generation (SHG) of the crystals were studied before and after irradiation. The dielectric constant was found to increase after irradiation. The DSC reveals that the melting point remains unaffected due to irradiation. The SHG efficiency of LASN was found to decrease with increase in radiation dose.

  2. Vertical alignment of liquid crystal through ion beam exposure on oxygen-doped SiC films deposited at room temperature

    SciTech Connect

    Son, Phil Kook; Park, Jeung Hun; Kim, Jae Chang; Yoon, Tae-Hoon; Rho, Soon Joon; Jeon, Back Kyun; Shin, Sung Tae; Kim, Jang Sub; Lim, Soon Kwon

    2007-09-03

    The authors report the vertical alignment of liquid crystal (LC) through the ion beam exposure on amorphous oxygen-doped SiC (SiOC) film surfaces deposited at room temperature. The optical transmittance of these films was similar to that of polyimide layers, but much higher than that of SiO{sub x} films. The light leakage of a LC cell aligned vertically on SiOC films was much lower than those of a LC cell aligned on polyimide layers or other inorganic films. They found that LC molecules align vertically on ion beam treated SiOC film when the roughness of the electrostatic force microscopy (EFM) data is high on the SiOC film surface, while they align homogeneously when the roughness of the EFM data is low.

  3. Wastewater treatment by batch adsorption method onto micro-particles of dried Withania frutescens plant as a new adsorbent.

    PubMed

    Chiban, Mohamed; Soudani, Amina; Sinan, Fouad; Persin, Michel

    2012-03-01

    A new adsorbent for removing metallic elements, nitrate and phosphate ions from municipal and industrial wastewaters has been investigated. This new adsorbent consists of micro-particles of dried Withania frutescens plant (<500 μm). Batch experiments were conducted to evaluate the removal of metallic elements and anions from raw wastewaters by W. frutescens particles. The results show that the micro-particles of W. frutescens plant presented a good adsorption of metallic elements, nitrate and phosphate ions from both real wastewaters. This adsorption increased with increasing of contact time. The percentage of metallic elements removal from industrial wastewater by W. frutescens plant was 98 ≈ 99% for Pb(II), 92 ≈ 93% for Cd(II), 91 ≈ 92% for Cu(II) and 92 ≈ 93% for Zn(II). The maximum adsorption capacity was dependent on the type of ions. The results also indicate that the values of chemical oxygen demand (COD) decrease after the contact with W. frutescens particles. Based on the results it can be concluded that the dried W. frutescens plant appears to be an economical and environmentally friendly material for wastewater treatment.

  4. Effects of negative air ions on oxygen uptake kinetics, recovery and performance in exercise: a randomized, double-blinded study

    NASA Astrophysics Data System (ADS)

    Nimmerichter, Alfred; Holdhaus, Johann; Mehnen, Lars; Vidotto, Claudia; Loidl, Markus; Barker, Alan R.

    2014-09-01

    Limited research has suggested that acute exposure to negatively charged ions may enhance cardio-respiratory function, aerobic metabolism and recovery following exercise. To test the physiological effects of negatively charged air ions, 14 trained males (age: 32 ± 7 years; : 57 ± 7 mL min-1 kg-1) were exposed for 20 min to either a high-concentration of air ions (ION: 220 ± 30 × 103 ions cm-3) or normal room conditions (PLA: 0.1 ± 0.06 × 103 ions cm-3) in an ionization chamber in a double-blinded, randomized order, prior to performing: (1) a bout of severe-intensity cycling exercise for determining the time constant of the phase II response ( τ) and the magnitude of the slow component (SC); and (2) a 30-s Wingate test that was preceded by three 30-s Wingate tests to measure plasma [adrenaline] (ADR), [nor-adrenaline] (N-ADR) and blood [lactate] (BLac) over 20 min during recovery in the ionization chamber. There was no difference between ION and PLA for the phase II τ (32 ± 14 s vs. 32 ± 14 s; P = 0.7) or SC (404 ± 214 mL vs 482 ± 217 mL; P = 0.17). No differences between ION and PLA were observed at any time-point for ADR, N-ADR and BLac as well as on peak and mean power output during the Wingate tests (all P > 0.05). A high-concentration of negatively charged air ions had no effect on aerobic metabolism during severe-intensity exercise or on performance or the recovery of the adrenergic and metabolic responses after repeated-sprint exercise in trained athletes.

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

    NASA Technical Reports Server (NTRS)

    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.

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

    NASA Astrophysics Data System (ADS)

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

    1994-11-01

    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.

  7. Influence of plasma-generated negative oxygen ion impingement on magnetron sputtered amorphous SiO{sub 2} thin films during growth at low temperatures

    SciTech Connect

    Macias-Montero, M.; Garcia-Garcia, F. J.; Alvarez, R.; Gil-Rostra, J.; Gonzalez, J. C.; Gonzalez-Elipe, A. R.; Palmero, A.; Cotrino, J.

    2012-03-01

    Growth of amorphous SiO{sub 2} thin films deposited by reactive magnetron sputtering at low temperatures has been studied under different oxygen partial pressure conditions. Film microstructures varied from coalescent vertical column-like to homogeneous compact microstructures, possessing all similar refractive indexes. A discussion on the process responsible for the different microstructures is carried out focusing on the influence of (i) the surface shadowing mechanism, (ii) the positive ion impingement on the film, and (iii) the negative ion impingement. We conclude that only the trend followed by the latter and, in particular, the impingement of O{sup -} ions with kinetic energies between 20 and 200 eV, agrees with the resulting microstructural changes. Overall, it is also demonstrated that there are two main microstructuring regimes in the growth of amorphous SiO{sub 2} thin films by magnetron sputtering at low temperatures, controlled by the amount of O{sub 2} in the deposition reactor, which stem from the competition between surface shadowing and ion-induced adatom surface mobility.

  8. First-principles study of oxygen adsorption and diffusion on the UN(001) surface

    NASA Astrophysics Data System (ADS)

    Nie, J. L.; Ao, L.; Zu, X. T.; Huang, H.; Liu, K. Z.

    2015-12-01

    First-principles calculations have been performed to study the interaction of oxygen with UN(001) surface. The molecule oxygen was found to dissociate spontaneously on all considered adsorption sites on the surface. Atomic oxygen (O) preferred to adsorb on a hollow site or the top of uranium ions, which were energetically degenerate. Adsorption on top of nitrogen (N) ion was found to be unstable which may be attributed to the repulsion of negatively charged O with the N anions. In comparison with those on α-U(001)surface at the same coverage, the adsorption of O on UN(001) surface was found to be less stable, being about 0.7 eV higher in adsorption energy. The diffusion barrier for O on the surface was found to be ∼0.5 eV, similar to those of α-U(001)surface. The penetration of O into the substrate was difficult with a high barrier of 2.86 eV. Analysis on the density of states (DOS) has shown that the adsorbed oxygen has strong chemical interaction with surface ions, characterized by the hybridization of O 2p states with N 2p and U 6d, U 5f states.

  9. RADIOLYSIS OF ORGANIC COMPOUNDS IN THE ADSORBED STATE

    DOEpatents

    Sutherland, J.W.; Allen, A.O.

    1961-10-01

    >A method of forming branch chained hydrocarbons by means of energetic penetrating radiation is described. A solid zeolite substrate is admixed with a cobalt ion and is irradiated with a hydrocarbon adsorbed therein. Upon irradiation with gamma rays, there is an increased yield of branched and lower molecular straight chain compounds. (AEC)

  10. Adsorbent Alkali Conditioning for Uranium Adsorption from Seawater. Adsorbent Performance and Technology Cost Evaluation

    SciTech Connect

    Tsouris, Costas; Mayes, Richard T.; Janke, Christopher James; Dai, Sheng; Das, S.; Liao, W. -P.; Kuo, Li-Jung; Wood, Jordana; Gill, Gary; Byers, Maggie Flicker; Schneider, Eric

    2015-09-30

    -flow natural seawater at the Pacific Northwest National Laboratory (PNNL). Fourier Transform Infrared (FTIR) spectroscopy, Nuclear Magnetic Resonance (NMR) spectroscopy, Scanning Electron Microscopy (SEM), and elemental analysis were used to characterize the adsorbent at different stages of adsorbent preparation and treatment. The study can be divided into two parts: (A) investigation of optimal parameters for KOH adsorbent conditioning and (B) investigation of other possible agents for alkali conditioning, including cost analysis on the basis of uranium production. In the first part of the study, tests with simulated seawater containing 8 ppm uranium showed that the uranium adsorption capacity increased with an increase in the KOH concentration and conditioning time and temperature at each of the KOH concentrations used. FTIR and solid state NMR studies indicated that KOH conditioning converts the amidoxime functional groups into more hydrophilic carboxylate. The longer the KOH conditioning time, up to three hours, the higher was the loading capacity from the simulated seawater solution which is composed of only uranyl, sodium, chloride, and carbonate ions. Marine testing with natural seawater, on the other hand, showed that the uranium adsorption capacity of the adsorbent increased with KOH conditioning temperature, and gradually decreased with increasing KOH conditioning time from one hour to three hours at 80 C. This behavior is due to the conversion of amidoxime to carboxylate. The carboxylate groups are needed to increase the hydrophilicity of the adsorbent; however, conversion of a significant amount of amidoxime to carboxylate leads to loss in selectivity toward uranyl ions. Thus, there is an optimum KOH conditioning time for each temperature at which an optimum ratio between amidoxime and carboxylate is reached. For the case of base conditioning with 0.44 M KOH at 80 C, the optimal conditioning time is 1 hour, with respect to the highest uranium loading capacity from

  11. Effect of Indium-Oxide Deposited Using an Oxygen Ion-Beam-Assisted-Deposition to Top-Emitting Organic Light-Emitting Diodes

    NASA Astrophysics Data System (ADS)

    Jeong, Chang Hyun; Lim, Jong Tae; Lee, June Hee; Kim, Mi Suk; Bae, Jeong Woon; Yeom, Geun Young

    2006-10-01

    Indium oxide thin films have potential applications as cathodes in top-emitting organic light-emitting diodes (TEOLEDs). This study examined the characteristics of transparent conducting indium oxide (IO) films deposited by an oxygen ion-beam-assisted-deposition (IBAD) as a function of the applied oxygen ion energy (Va). When TEOLED devices consisting of glass/Ag (100 nm)/ITO (125 nm)/2-TNATA (30 nm)/NPB (15 nm)/Alq3 (55 nm)/LiF (1 nm)/Al (2 nm)/Au (20 nm)/IO (100 nm) were fabricated at a lower Va, a lower turn-on voltage was observed even though the maximum luminance (32,000 cd/m2) was similar one another. A Va of approximately +50 V produced an IO film with a resistivity of 8.5× 10-4 Ω\\cdotcm and a transmittance of 85%. The definition (I-V) characteristics of TEOLED devices with a cathode layer of Al (2 nm)/Au (20 nm)/IO (100 nm) were similar to the device fabricated with Al (2 nm)/Au (20 nm) only.

  12. Polyoxometalate-enhanced oxidation of organic compounds by nanoparticulate zero-valent iron and ferrous ion in the presence of oxygen.

    PubMed

    Lee, Changha; Keenan, Christina R; Sedlak, David L

    2008-07-01

    In the presence of oxygen, organic compounds can be oxidized by zerovalent iron or dissolved Fe(II). However, this process is not a very effective means of degrading contaminants because the yields of oxidants are usually low (i.e., typically less than 5% of the iron added is converted into oxidants capable of transforming organic compounds). The addition of polyoxometalate (POM) greatly increases the yield of oxidants in both systems. The mechanism of POM enhancement depends on the solution pH. Under acidic conditions, POM mediates the electron transfer from nanoparticulate zerovalent iron (nZVI) or Fe(II) to oxygen, increasing the production of hydrogen peroxide, which is subsequently converted to hydroxyl radical through the Fenton reaction. At neutral pH values, iron forms a complex with POM, preventing iron precipitation on the nZVI surface and in bulk solution. At pH 7, the yield of oxidant approaches the theoretical maximum in the nZVI/O2 and the Fe(II)/O2 systems when POM is present, suggesting that coordination of iron by POM alters the mechanism of the Fenton reaction by converting the active oxidant from ferryl ion to hydroxyl radical. Comparable enhancements in oxidant yields are also observed when nZVI or Fe(II) is exposed to oxygen in the presence of silica-immobilized POM. PMID:18678027

  13. The influence of Atomic Oxygen on the Figure of Merit of Indium Tin Oxide thin Films grown by reactive Dual Ion Beam Sputtering

    NASA Astrophysics Data System (ADS)

    Geerts, Wilhelmus; Simpson, Nelson; Woodall, Allen; Compton, Maclyn

    2014-03-01

    Indium Tin Oxide (ITO) is a transparent conducting oxide that is used in flat panel displays and optoelectronics. Highly conductive and transparent ITO films are normally produced by heating the substrate to 300 Celsius during deposition excluding plastics to be used as a substrate material. We investigated whether high quality ITO films can be sputtered at room temperature using atomic instead of molecular oxygen. The films were deposited by dual ion beam sputtering (DIBS). During deposition the substrate was exposed to a molecular or an atomic oxygen flux. Microscope glass slides and silicon wafers were used as substrates. A 29 nm thick SIO2 buffer layer was used. Optical properties were measured with a M2000 Woollam variable angle spectroscopic ellipsometer. Electrical properties were measured by linear four point probe using a Jandel 4pp setup employing silicon carbide electrodes, high input resistance, and Keithley low bias current buffer amplifiers. The figure of merit (FOM), i.e. the ratio of the conductivity and the average optical absorption coefficient (400-800 nm), was calculated from the optical and electric properties and appeared to be 1.2 to 5 times higher for the samples sputtered with atomic oxygen. The largest value obtained for the FOM was 0.08 reciprocal Ohms. The authors would like to thank the Research Corporation for Financial Support.

  14. Assessment of spatial variability of major-ion concentrations and del oxygen-18 values in surface snow, Upper Fremont Glacier, Wyoming, USA

    USGS Publications Warehouse

    Naftz, D.L.; Schuster, P.F.; Reddy, M.M.

    1994-01-01

    One hundred samples were collected from the surface of the Upper Fremont Glacier at equally spaced intervals defined by an 8100m2 snow grid to asesss the significance of lateral variability in major-ion concentrations and del oxygen-18 values. Comparison of the observed variability of each chemical constituent to the variability expected by measurement error indicated substantial lateral variability with the surface-snow layer. Results of the nested ANOVA indicate most of the variance for every constituent is in the values grouped at the two smaller geographic scales (between 506m2 and within 506m2 sections). The variance data from the snow grid were used to develop equations to evaluate the significance of both positive and negative concentration/value peaks of nitrate and del oxygen-18 with depth, in a 160m ice core. Values of del oxygen-18 in the section from 110-150m below the surface consistently vary outside the expected limits and possibly represents cooler temperatures during the Little Ice Age from about 1810 to 1725 A.D. -from Authors

  15. Selective photooxidation of hydrocarbons in zeolites by oxygen

    DOEpatents

    Frei, Heinz; Blatter, Fritz; Sun, Hai

    1998-01-01

    A selective photooxidation process for the conversion of hydrocarbon molecules to partially oxygenated derivatives, which comprises the steps of adsorbing a hydrocarbon and oxygen onto a dehydrated zeolite support matrix to form a hydrocarbon-oxygen contact pair, and subsequently exposing the hydrocarbon-oxygen contact pair to visible light, thereby forming a partially oxygenated derivative.

  16. The precipitation of keV energetic oxygen ions at Mars and their effects during the comet Siding Spring approach

    NASA Astrophysics Data System (ADS)

    Gronoff, Guillaume; Rahmati, Ali; Wedlund, Cyril Simon; Mertens, Christopher J.; Cravens, Thomas E.; Kallio, Esa

    2014-07-01

    Comet Siding Spring C/2013 A1 will pass Mars on 19 October 2014, entailing particle and dust precipitation in the Martian upper atmosphere and a potential dust hazard for orbiters. An estimate of the flux of energetic O+ ions picked up by the solar wind from the cometary coma is shown, with an increase of the O+ flux above 50 keV by 2 orders of magnitude. While the ionization of Mars' upper atmosphere by precipitating O+ ions is expected to be negligible compared to solar EUV-XUV ionization, it is of the same order of magnitude at 110 km altitude during the cometary passage, leading to detectable increases in ionospheric densities. Cometary O+ pickup ion precipitation is expected to be the major nightside ionization source, creating a temporary ionosphere and a global airglow. These effects are dependent on the solar and cometary activities at the time of the encounter.

  17. The entropies of adsorbed molecules.

    PubMed

    Campbell, Charles T; Sellers, Jason R V

    2012-10-31

    Adsorbed molecules are involved in many reactions on solid surface that are of great technological importance. As such, there has been tremendous effort worldwide to learn how to predict reaction rates and equilibrium constants for reactions involving adsorbed molecules. Theoretical calculation of both the rate and equilibrium constants for such reactions requires knowing the entropy and enthalpy of the adsorbed molecule. While much effort has been devoted to measuring and calculating the enthalpies of well-defined adsorbates, few measurements of the entropies of adsorbates have been reported. We present here a new way to determine the standard entropies of adsorbed molecules (S(ad)(0)) on single crystal surfaces from temperature programmed desorption data, prove its accuracy by comparison to entropies measured by equilibrium methods, and apply it to published data to extract new entropies. Most importantly, when combined with reported entropies, we find that at high coverage, they linearly track the entropy of the gas-phase molecule at the same temperature (T), such that S(ad)(0)(T) = 0.70 S(gas)(0)(T) - 3.3R (R = the gas constant), with a standard deviation of only 2R over a range of 50R. These entropies, which are ~2/3 of the gas, are huge compared to most theoretical predictions. This result can be extended to reliably predict prefactors in the Arrhenius rate constant for surface reactions involving such species, as proven here for desorption. PMID:23033909

  18. Application of central composite design for simultaneous removal of methylene blue and Pb2+ ions by walnut wood activated carbon

    NASA Astrophysics Data System (ADS)

    Ghaedi, M.; Mazaheri, H.; Khodadoust, S.; Hajati, S.; Purkait, M. K.

    2015-01-01

    Activated carbon was prepared from walnut wood which was locally available, non-toxic, abundant and cheap. This new adsorbent was characterized using BET, FTIR and SEM. Point of zero charge (pHpzc) and oxygen containing functional groups were also determined. The prepared adsorbent was applied for simultaneous removal of Pb2+ ions and methylene blue (MB) dye from aqueous solution. The prominent effect and interaction of variables such as amount of adsorbent, contact time, concentration of MB and Pb2+ ions were optimized by central composite design. The equilibrium data obtained at optimum condition were fitted to conventional isotherm models and found that Langmuir model was the best fitted isotherm. Kinetic data were fitted using various models. It was revealed that the adsorption rate follows pseudo-second order kinetic model and intraparticle diffusion model.

  19. Increases in reactive oxygen species enhance vascular endothelial cell migration through a mechanism dependent on the transient receptor potential melastatin 4 ion channel.

    PubMed

    Sarmiento, Daniela; Montorfano, Ignacio; Cerda, Oscar; Cáceres, Mónica; Becerra, Alvaro; Cabello-Verrugio, Claudio; Elorza, Alvaro A; Riedel, Claudia; Tapia, Pablo; Velásquez, Luis A; Varela, Diego; Simon, Felipe

    2015-03-01

    A hallmark of severe inflammation is reactive oxygen species (ROS) overproduction induced by increased inflammatory mediators secretion. During systemic inflammation, inflammation mediators circulating in the bloodstream interact with endothelial cells (ECs) raising intracellular oxidative stress at the endothelial monolayer. Oxidative stress mediates several pathological functions, including an exacerbated EC migration. Because cell migration critically depends on calcium channel-mediated Ca(2+) influx, the molecular identification of the calcium channel involved in oxidative stress-modulated EC migration has been the subject of intense investigation. The transient receptor potential melastatin 4 (TRPM4) protein is a ROS-modulated non-selective cationic channel that performs several cell functions, including regulating intracellular Ca(2+) overload and Ca(2+) oscillation. This channel is expressed in multiple tissues, including ECs, and contributes to the migration of certain immune cells. However, whether the TRPM4 ion channel participates in oxidative stress-mediated EC migration is not known. Herein, we investigate whether oxidative stress initiates or enhances EC migration and study the role played by the ROS-modulated TRPM4 ion channel in oxidative stress-mediated EC migration. We demonstrate that oxidative stress enhances, but does not initiate, EC migration in a dose-dependent manner. Notably, we demonstrate that the TRPM4 ion channel is critical in promoting H2O2-enhanced EC migration. These results show that TRPM4 is a novel pharmacological target for the possible treatment of severe inflammation and other oxidative stress-mediated inflammatory diseases.

  20. Anti-leukemia activity of PVP-coated silver nanoparticles via generation of reactive oxygen species and release of silver ions.

    PubMed

    Guo, Dawei; Zhu, Lingying; Huang, Zhihai; Zhou, Haixia; Ge, Yue; Ma, Wenjuan; Wu, Jie; Zhang, Xiuyan; Zhou, Xuefeng; Zhang, Yu; Zhao, Yun; Gu, Ning

    2013-10-01

    Silver nanoparticles (AgNPs) have anti-cancer effect. However, whether and how these particles could inhibit the growth of acute myeloid leukemia (AML) cells is unclear. In the present study, we prepared AgNPs with various sizes and investigated their cytotoxic effect on AML cells. We found that AgNPs could inhibit the viability of AML cells including the isolates from AML patients. AgNPs caused the production of reactive oxygen species (ROS), losses of mitochondrial membrane potential (MMP), DNA damage and apoptosis. Both vitamin C (Vit C) and N-acetyl-L-cysteine (NAC) could completely reverse the generation of ROS upon AgNPs, however only NAC but not Vit C could protect the cells from losses of MMP, DNA damage and apoptosis thoroughly. Similar results were obtained when cells were treated with silver ions alone. As NAC was not only an antioxidant to scavenge ROS but also a silver ion chelator, these data supported the model that both generation of ROS and release of silver ions played critical roles in the AgNPs-induced cytotoxic effect against AML cells. Taken together, this work elucidated the cytotoxic effect of AgNPs on AML cells and their underlying mechanism and might have significant impact on AML treatment.

  1. Li-ion storage dynamics in metastable nanostructured Li2FeSiO4 cathode: Antisite-induced phase transition and lattice oxygen participation

    NASA Astrophysics Data System (ADS)

    Lu, Xia; Chiu, Hsien-Chieh; Arthur, Zachary; Zhou, Jigang; Wang, Jian; Chen, Ning; Jiang, De-Tong; Zaghib, Karim; Demopoulos, George P.

    2016-10-01

    Li2FeSiO4 (LFS) has drawn much attention as cathode for high capacity Li-ion batteries. Even though significant volume of study has been devoted to its crystal chemistry and electrochemistry, many questions relating to its Li-ion storage dynamics remain yet to be fully elucidated. In this context, synchrotron-based X-ray diffraction and absorption spectroscopies are employed to characterize the phase stability and charge compensation mechanism in a metastable Li2FeSiO4 nanostructured cathode as a function of state-of-charge (Li2-xFeSiO4, x = 0, 0.25, 0.50, 0.75, 1.0) and cycling at very low current. The results demonstrate (i) no detectable phase transition from monoclinic to orthorhombic phase during the first charge-discharge cycle but rather formation of antisite defects that progressively induce phase transformation after several electrochemical cycles; (ii) characteristics of solid solution Li-ion storage (Li2-xFeSiO4, x = 0-1); and (iii) the charge compensation for the first Li extraction does not come solely from the ferrous to ferric conversion, but interestingly from prominent participation of lattice oxygen as well that appears to destabilize the cycled LFS structure with significant performance implications.

  2. Catalytic therapy of cancer by ascorbic acid involves redox cycling of exogenous/endogenous copper ions and generation of reactive oxygen species.

    PubMed

    Hadi, S M; Ullah, M F; Shamim, U; Bhatt, S H; Azmi, A S

    2010-01-01

    Catalytic therapy is a cancer treatment modality based on the generation of reactive oxygen species (ROS) through administration of ascorbate/medicinal herbal extracts and copper. It is known that antioxidants such as ascorbate also exhibit prooxidant activity in the presence of transition metals such as copper. Based on our work and that in the literature, in this review we propose a mechanism for the cytotoxic action of ascorbate against cancer cells. It involves redox cycling of exogenous/endogenous copper ions and the consequent generation of ROS leading to oxidative DNA breakage. Using human peripheral lymphocytes and the Comet assay, we have shown that ascorbic acid is able to cause oxidative breakage in cellular DNA. Such DNA degradation is inhibited by neocuproine (a Cu(I) sequestering agent) and scavengers of ROS indicating that the cellular DNA breakage involves the generation of Cu(I) and formation of ROS. Similar results are also obtained with plant polyphenol antioxidants that are important constituents of medicinal herbal extracts. Copper is an essential component of chromatin and can take part in redox reactions. It is well established that tissue, cellular and serum copper levels are considerably elevated in various malignancies. Therefore, cancer cells may be more subject to electron transfer between copper ions and ascorbate/plant polyphenols to generate ROS. In this review we cite evidence to indicate that in catalytic therapy cytotoxic action against cancer cells involves redox cycling of exogenous/endogenous copper ions.

  3. Increases in reactive oxygen species enhance vascular endothelial cell migration through a mechanism dependent on the transient receptor potential melastatin 4 ion channel.

    PubMed

    Sarmiento, Daniela; Montorfano, Ignacio; Cerda, Oscar; Cáceres, Mónica; Becerra, Alvaro; Cabello-Verrugio, Claudio; Elorza, Alvaro A; Riedel, Claudia; Tapia, Pablo; Velásquez, Luis A; Varela, Diego; Simon, Felipe

    2015-03-01

    A hallmark of severe inflammation is reactive oxygen species (ROS) overproduction induced by increased inflammatory mediators secretion. During systemic inflammation, inflammation mediators circulating in the bloodstream interact with endothelial cells (ECs) raising intracellular oxidative stress at the endothelial monolayer. Oxidative stress mediates several pathological functions, including an exacerbated EC migration. Because cell migration critically depends on calcium channel-mediated Ca(2+) influx, the molecular identification of the calcium channel involved in oxidative stress-modulated EC migration has been the subject of intense investigation. The transient receptor potential melastatin 4 (TRPM4) protein is a ROS-modulated non-selective cationic channel that performs several cell functions, including regulating intracellular Ca(2+) overload and Ca(2+) oscillation. This channel is expressed in multiple tissues, including ECs, and contributes to the migration of certain immune cells. However, whether the TRPM4 ion channel participates in oxidative stress-mediated EC migration is not known. Herein, we investigate whether oxidative stress initiates or enhances EC migration and study the role played by the ROS-modulated TRPM4 ion channel in oxidative stress-mediated EC migration. We demonstrate that oxidative stress enhances, but does not initiate, EC migration in a dose-dependent manner. Notably, we demonstrate that the TRPM4 ion channel is critical in promoting H2O2-enhanced EC migration. These results show that TRPM4 is a novel pharmacological target for the possible treatment of severe inflammation and other oxidative stress-mediated inflammatory diseases. PMID:24518820

  4. Mechanism of deoxyribonucleic acid breakage induced by 4'-(9-acridinylamino)methanesulfon-m-anisidide and copper: role for cuprous ion and oxygen free radicals

    SciTech Connect

    Wong, A.; Huang, C.H.; Crooke, S.T.

    1984-06-19

    4-(9-Acridinylamino)methanesulfon-m-anisidide (mAMSA) interacts with Cu(II) ions, as indicated by changes in the mAMSA absorption spectrum induced by Cu(II). The spectral changes are due to the oxidation of mAMSA by Cu(II), resulting in an oxidized mAMSA product and Cu(I). Cu(I) plays an important role in the mAMSA-Cu(II)-induced DNA breakage, since in the presence of neocuproine the DNA breakage is inhibited. Up to 200 ..mu..M, Cu(I) by itself is virtually ineffective, in contrast to the mixture of mAMSA and Cu(II). This suggests that mAMSA, aside from reducing Cu(II) to Cu(I), may play a role in mediating DNA breakage. The DNA breakage was reduced in partially anaerobic conditions, indicating the involvement of molecular oxygen. Catalase and 4,5-dihydroxy-1,2-benzenedisulfonate inhibited the DNA breakage completely, indicating that hydrogen peroxide and superoxide radicals mediate DNA breakage. 1,3-Diazabicyclo(2.2.2)octane partially inhibited the breakage, suggesting that singlet oxygen is involved. The available evidence supports a mechanism indicating the formation of a DNA x mAMSA x Cu(II) ternary complex and the subsequent oxidation-reduction of the complex to form DNA x mAQDI x Cu(I). The oxidation of the complexed Cu(I) may result in reduction of oxygen to oxygen free radicals which induce DNA breaks.

  5. Oxidative response of human monocytes and macrophages cultured under low oxygen culture conditions to ion parametric resonance magnetic fields.

    EPA Science Inventory

    INTRODUCTION One proposed mechanism of action of electromagnetic fields (EMFs) on biological systems is the Ion Parametric Resonance (IPR) model, which has been experimentally validated in neuronal PC-12 cells [1, 2]. It proposes that when applied EMFs are tuned to resonate with...

  6. Novel adsorbent applicability for decontamination of printing wastewater

    NASA Astrophysics Data System (ADS)

    Kiurski, Jelena; Oros, Ivana; Ranogajec, Jonjaua; Kecic, Vesna

    2013-04-01

    Adsorption capacity of clayey minerals can be enhanced by replacing the natural exchangeable cations with organic cations, which makes the clay surface more hydrophobic. Different solids such as activated carbon, clay minerals, zeolites, metal oxides and organic polymers have been tested as effective adsorbents. On a global scale, clays have a large applicability for decontamination, purification of urban and industrial residual waters, protection of waste disposal areas, and purification of industrial gases and so on. Clay derivative materials with high adsorption capacities are very attractive from an economical point of view. Due to the economic constraints, a development of cost effective and clean processes is desired. Adsorption processes has proved to be the most effective, especially for effluents with moderate and low heavy metal concentrations, as like as in printing wastewaters. Among several removal technologies, the adsorption of Zn(II) ion onto NZ, B, pure C and C with PEG 600 addition could be of great importance for the printing wastewaters purification. However, the newly designed adsorbent of the defined pore size distribution and phase structure considered as the most suitable material for Zn(II) ion removal. The values of distribution coefficient (Kd) increased with decreasing of the adsorbent amount. The Kd values depend also on the type of used adsorbent, the following increased order is obtained: NZ < B = pure C < C with PEG 600 addition. The adsorption equilibrium data of Zn(II) ion on NZ, B, pure C and C with PEG 600 were analyzed in terms of the Freundlich, Langmuir and Dubinin-Kaganer-Radushkevich (DKR) isotherm models. The characteristic parameters for each isotherms and related correlation coefficients were determined. The values of correlation coefficient (R2) indicated the following order of the isotherm models: Freundlich > Langmuir > DKR. The study also showed that the fired clay modified with PEG 600 addition has great potential

  7. UV-induced protonation of molecules adsorbed on ice surfaces at low temperature.

    PubMed

    Moon, Eui-Seong; Lee, Chang-Woo; Kim, Joon-Ki; Park, Seong-Chan; Kang, Heon

    2008-05-21

    UV irradiation of ice films adsorbed with methylamine molecules induces protonation of the adsorbate molecules at low temperature (50-130 K). The observation indicates that long-lived protonic defects are created in the ice film by UV light, and they transfer protons to the adsorbate molecules via tunneling mechanism at low temperature. The methylammonium ion formed by proton transfer remains to be stable at the ice surface. It is suggested that this solid-phase protonation might play a significant role in the production of molecular ions in interstellar clouds.

  8. The effect of cavity tuning on oxygen beam currents of an A-ECR type 14 GHz electron cyclotron resonance ion source

    NASA Astrophysics Data System (ADS)

    Tarvainen, O.; Orpana, J.; Kronholm, R.; Kalvas, T.; Laulainen, J.; Koivisto, H.; Izotov, I.; Skalyga, V.; Toivanen, V.

    2016-09-01

    The efficiency of the microwave-plasma coupling plays a significant role in the production of highly charged ion beams with electron cyclotron resonance ion sources (ECRISs). The coupling properties are affected by the mechanical design of the ion source plasma chamber and microwave launching system, as well as damping of the microwave electric field by the plasma. Several experiments attempting to optimize the microwave-plasma coupling characteristics by fine-tuning the frequency of the injected microwaves have been conducted with varying degrees of success. The inherent difficulty in interpretation of the frequency tuning results is that the effects of microwave coupling system and the cavity behavior of the plasma chamber cannot be separated. A preferable approach to study the effect of the cavity properties of the plasma chamber on extracted beam currents is to adjust the cavity dimensions. The results of such cavity tuning experiments conducted with the JYFL 14 GHz ECRIS are reported here. The cavity properties were adjusted by inserting a conducting tuner rod axially into the plasma chamber. The extracted beam currents of oxygen charge states O3+-O7+ were recorded at various tuner positions and frequencies in the range of 14.00-14.15 GHz. It was observed that the tuner position affects the beam currents of high charge state ions up to several tens of percent. In particular, it was found that at some tuner position / frequency combinations the plasma exhibited "mode-hopping" between two operating regimes. The results improve the understanding of the role of plasma chamber cavity properties on ECRIS performances.

  9. Oxygen foreshock of Mars

    NASA Astrophysics Data System (ADS)

    Yamauchi, M.; Lundin, R.; Frahm, R. A.; Sauvaud, J.-A.; Holmström, M.; Barabash, S.

    2015-12-01

    Mars Express (MEX) has operated for more than 10 years in the environment of Mars, providing solar wind ion observations from the Analyzer of Space Plasmas and Energetic Atoms experiment's Ion Mass Analyser (IMA). On 21 September 2008, MEX/IMA detected foreshock-like discrete distributions of oxygen ions at around 1 keV in the solar wind attached to the bow shock and this distribution was observed continuously up to more than 2000 km from the bow shock. Foreshock-like protons are also observed but at a shifted location from the oxygen by about 1000 km, at a slightly higher energy, and flowing in a slightly different direction than the oxygen ions. Both protons and oxygen ions are flowing anti-sunward at different angles with respect to the solar wind direction. This is the first time that a substantial amount of planetary oxygen is observed upstream of the bow shock. Although rare, this is not the only IMA observation of foreshock-like oxygen: oxygen ions are sometimes observed for a short period of time (<5 min) inside the foreshock region. These observations suggest a new escape channel for planetary ions through the acceleration in the bow shock-magnetosheath region.

  10. Solid state oxygen sensor

    DOEpatents

    Garzon, Fernando H.; Chung, Brandon W.; Raistrick, Ian D.; Brosha, Eric L.

    1996-01-01

    Solid state oxygen sensors are provided with a yttria-doped zirconia as an electrolyte and use the electrochemical oxygen pumping of the zirconia electrolyte. A linear relationship between oxygen concentration and the voltage arising at a current plateau occurs when oxygen accessing the electrolyte is limited by a diffusion barrier. A diffusion barrier is formed herein with a mixed electronic and oxygen ion-conducting membrane of lanthanum-containing perovskite or zirconia-containing fluorite. A heater may be used to maintain an adequate oxygen diffusion coefficient in the mixed conducting layer.

  11. Solid state oxygen sensor

    DOEpatents

    Garzon, F.H.; Chung, B.W.; Raistrick, I.D.; Brosha, E.L.

    1996-08-06

    Solid state oxygen sensors are provided with a yttria-doped zirconia as an electrolyte and use the electrochemical oxygen pumping of the zirconia electrolyte. A linear relationship between oxygen concentration and the voltage arising at a current plateau occurs when oxygen accessing the electrolyte is limited by a diffusion barrier. A diffusion barrier is formed herein with a mixed electronic and oxygen ion-conducting membrane of lanthanum-containing perovskite or zirconia-containing fluorite. A heater may be used to maintain an adequate oxygen diffusion coefficient in the mixed conducting layer. 4 figs.

  12. Ion-exchange method in the collection of nitrate from freshwater ecosystems for nitrogen and oxygen isotope analysis: a review.

    PubMed

    Li, Wen-Bing; Song, Yao-Bin; Xu, Hong-Ke; Chen, Ling-Yun; Dai, Wen-Hong; Dong, Ming

    2015-07-01

    Nitrate (NO3(-)) contamination of freshwater is considered one of the most prevalent global environmental problems. Dual stable isotopic compositions (δ(15)N and δ(18)O) of NO3(-) can provide helpful information and have been well documented as being a powerful tool to track the source of NO3(-) in freshwater ecosystems. The ion-exchange method is a reliable and precise technique for measuring the δ(15)N and δ(18)O of NO3(-) and has been widely employed to collect NO3(-) from freshwater ecosystems. This review summarizes and presents the principles, affecting factors and corresponding significant improvements of the ion-exchange method. Finally, potential improvements and perspectives for the applicability of this method are also discussed, as are suggestions for further research and development drawn from the overall conclusions.

  13. Single-Molecule Imaging of Iron-Phthalocyanine-Catalyzed Oxygen Reduction Reaction by in Situ Scanning Tunneling Microscopy.

    PubMed

    Gu, Jing-Ying; Cai, Zhen-Feng; Wang, Dong; Wan, Li-Jun

    2016-09-27

    We report herein an in situ electrochemical scanning tunneling microscopy (ECSTM) investigation of iron-phthalocyanine (FePc)-catalyzed oxygen reduction reaction (ORR). A highly ordered FePc adlayer is revealed on a Au(111) electrode. The center ions in the FePc adlayer show uniform high contrast in an oxygen-saturated electrolyte, which is attributed to the formation of an FePc-O2 complex. In situ STM results reveal the sharp contrast change upon shifting the electrode potential to trigger the ORR. Theoretical simulation has supplied further evidence for the contrast difference of the adsorbed FePc species. PMID:27508323

  14. Single-Molecule Imaging of Iron-Phthalocyanine-Catalyzed Oxygen Reduction Reaction by in Situ Scanning Tunneling Microscopy.

    PubMed

    Gu, Jing-Ying; Cai, Zhen-Feng; Wang, Dong; Wan, Li-Jun

    2016-09-27

    We report herein an in situ electrochemical scanning tunneling microscopy (ECSTM) investigation of iron-phthalocyanine (FePc)-catalyzed oxygen reduction reaction (ORR). A highly ordered FePc adlayer is revealed on a Au(111) electrode. The center ions in the FePc adlayer show uniform high contrast in an oxygen-saturated electrolyte, which is attributed to the formation of an FePc-O2 complex. In situ STM results reveal the sharp contrast change upon shifting the electrode potential to trigger the ORR. Theoretical simulation has supplied further evidence for the contrast difference of the adsorbed FePc species.

  15. Direct Production of Electron-Positron Pairs by 200-GeV/Nucleon Oxygen and Sulfur Ions in Nuclear Emulsion

    NASA Technical Reports Server (NTRS)

    Derrickson, J. H.; Eby, P. B.; Moon, K. H.; Parnell, T. A.; King, D. T.; Gregory, J. C.; Takahashi, Y.; Ogata, T.

    1995-01-01

    Measurements of direct Coulomb electron-positron pair production have been made on the tracks of relativistic heavy ions in nuclear track emulsion. Tracks of 0(16) and S(32) at 200 GeV/nucleon were studied. The measured total cross sections and energy and emission angle distributions for the pair members are compared to theoretical predictions. The data are consistent with some recent calculations when knock-on electron contamination is accounted for.

  16. Rotary adsorbers for continuous bulk separations

    DOEpatents

    Baker, Frederick S.

    2011-11-08

    A rotary adsorber for continuous bulk separations is disclosed. The rotary adsorber includes an adsorption zone in fluid communication with an influent adsorption fluid stream, and a desorption zone in fluid communication with a desorption fluid stream. The fluid streams may be gas streams or liquid streams. The rotary adsorber includes one or more adsorption blocks including adsorbent structure(s). The adsorbent structure adsorbs the target species that is to be separated from the influent fluid stream. The apparatus includes a rotary wheel for moving each adsorption block through the adsorption zone and the desorption zone. A desorption circuit passes an electrical current through the adsorbent structure in the desorption zone to desorb the species from the adsorbent structure. The adsorbent structure may include porous activated carbon fibers aligned with their longitudinal axis essentially parallel to the flow direction of the desorption fluid stream. The adsorbent structure may be an inherently electrically-conductive honeycomb structure.

  17. Oxygen ion irradiation on AlGaN/GaN heterostructure grown on silicon substrate by MOCVD method

    SciTech Connect

    Ramesh, R.; Arivazhagan, P.; Balaji, M.; Baskar, K.; Asokan, K.

    2015-06-24

    In the present work, we have reported 100 MeV O{sup 7+} ion irradiation with 1×10{sup 12} and 5×10{sup 12} ions/cm{sup 2} fluence on AlGaN/GaN heterostructures grown on silicon substrate by Metal Organic Chemical Vapour Deposition (MOCVD). The Irradiated samples were characterized by High Resolution X-Ray Diffraction (HRXRD), Atomic Force Microscope (AFM) and Photoluminescence (PL). Crystalline quality has been analysed before and after irradiation using HRXRD. Different kinds of morphology are attributed to specific type of dislocations using the existing models available in the literature. A sharp band-edge emission in the as grown samples was observed at ∼3.4 eV in GaN and 3.82 for AlGaN. The band-edge absorption intensity reduced due to irradiation and these results have been discussed in view of the damage created by the incident ions. In general the effect of irradiation induced-damages were analysed as a function of material properties. A possible mechanism responsible for the observations has been discussed.

  18. Assessment of mercury toxicity by the changes in oxygen consumption and ion levels in the freshwater snail, Pila globosa, and the mussel, Lamellidens marginalis

    SciTech Connect

    Sivaramakrishna, B.; Radhakrishnaiah, K.; Suresh, A. )

    1991-06-01

    There are many studies on mercury toxicity in freshwater fishes but very few on freshwater molluscs (Wright 1978) though they serve as bio-indicators of metal pollution. A few reports on marine gastropods and bivalves indicated the importance of these animals in metal toxicity studies. Hence, in the present study, the level of tolerance of the freshwater gastropod Pila globosa and of a freshwater bivalve Lamellidens marginalis mercury at lethal and sublethal levels was determined and compared with the rate of whole animal oxygen consumption and the level of sodium, potassium and calcium ions in the hepatopancreas and the foot of these animals. As the period of exposure is one of the important factors in toxicity studies, the level of tolerance was determined at 120 hours of exposure and the other parameters were analyzed at 1, 3 and 5 days in lethal and at 1, 7 and 15 days in sublethal concentrations.

  19. Enhanced sulfur tolerance of nickel-based anodes for oxygen-ion conducting solid oxide fuel cells by incorporating a secondary water storing phase.

    PubMed

    Wang, Feng; Wang, Wei; Qu, Jifa; Zhong, Yijun; Tade, Mose O; Shao, Zongping

    2014-10-21

    In this work, a Ni+BaZr(0.4)Ce(0.4)Y(0.2)O(3-δ) (Ni+BZCY) anode with high water storage capability is used to increase the sulfur tolerance of nickel electrocatalysts for solid oxide fuel cells (SOFCs) with an oxygen-ion conducting Sm(0.2)Ce(0.8)O(1.9) (SDC) electrolyte. Attractive power outputs are still obtained for the cell with a Ni+BZCY anode that operates on hydrogen fuels containing 100-1000 ppm of H2S, while for a similar cell with a Ni+SDC anode, it displays a much reduced performance by introducing only 100 ppm of H2S into hydrogen. Operating on a hydrogen fuel containing 100 ppm of H2S at 600 °C and a fixed current density of 200 mA cm(-2), a stable power output of 148 mW cm(-2) is well maintained for a cell with a Ni+BZCY anode within a test period of 700 min, while it was decreased from an initial value of 137 mW cm(-2) to only 81 mW cm(-2) for a similar cell with a Ni+SDC anode after a test period of only 150 min. After the stability test, a loss of the Ni percolating network and reaction between nickel and sulfur appeared over the Ni+SDC anode, but it is not observed for the Ni+BZCY anode. This result highly promises the use of water-storing BZCY as an anode component to improve sulfur tolerance for SOFCs with an oxygen-ion conducting SDC electrolyte.

  20. Ferritin protein nanocages use ion channels, catalytic sites, and nucleation channels to manage iron/oxygen chemistry.

    PubMed

    Theil, Elizabeth C

    2011-04-01

    The ferritin superfamily is composed of ancient, nanocage proteins with an internal cavity, 60% of total volume, that reversibly synthesize solid minerals of hydrated ferric oxide; the minerals are iron concentrates for cell nutrition as well as antioxidants due to ferrous and oxygen consumption during mineralization. The cages have multiple iron entry/exit channels, oxidoreductase enzyme sites, and, in eukaryotes, Fe(III)O nucleation channels with clustered exits that extend protein activity to include facilitated mineral growth. Ferritin protein cage differences include size, amino acid sequence, and location of the active sites, oxidant substrate and crystallinity of the iron mineral. Genetic regulation depends on iron and oxygen signals, which in animals includes direct ferrous signaling to RNA to release and to ubiquitin-ligases to degrade the protein repressors. Ferritin biosynthesis forms, with DNA, mRNA and the protein product, a feedback loop where the genetic signals are also protein substrates. The ferritin protein nanocages, which are required for normal iron homeostasis and are finding current use in the delivery of nanodrugs, novel nanomaterials, and nanocatalysts, are likely contributors to survival and success during the transition from anaerobic to aerobic life.

  1. Characterization of oxygenated derivatives of isoprene related to 2-methyltetrols in Amazonian aerosols using trimethylsilylation and gas chromatography/ion trap mass spectrometry.

    PubMed

    Wang, Wu; Kourtchev, Ivan; Graham, Bim; Cafmeyer, Jan; Maenhaut, Willy; Claeys, Magda

    2005-01-01

    In the present study, we have tentatively identified the structures of three oxygenated derivatives of isoprene in Amazonian rain forest aerosols as the C(5) alkene triols, 2-methyl-1,3,4-trihydroxy-1-butene (cis and trans) and 3-methyl-2,3,4-trihydroxy-1-butene. The formation of these oxygenated derivatives of isoprene can be explained by acid-catalyzed ring opening of epoxydiol derivatives of isoprene, namely, 1,2-epoxy-2-methyl-3,4-dihydroxybutane and 1,2-dihydroxy-2-methyl-3,4-epoxybutane. The structural proposals of the C(5) alkene triols were based on chemical derivatization reactions and detailed interpretation of electron and chemical ionization mass spectral data, including data obtained from first-order mass spectra, deuterium labeling of the trimethylsilyl methyl groups, and MS(2) ion trap experiments. The characterization of 2-methyl-1,3,4-trihydroxy-1-butene (cis and trans) and 3-methyl-2,3,4-trihydroxy-1-butene in forest aerosols is important from an atmospheric chemistry viewpoint in that these compounds hint at the formation of intermediate isomeric epoxydiol derivatives of isoprene and as such provide mechanistic insights into the formation of the previously reported 2-methyltetrols through photooxidation of isoprene.

  2. Role of associated defects in oxygen ion conduction and surface exchange reaction for epitaxial samaria-doped ceria thin films as catalytic coatings

    DOE PAGES

    Yang, Nan; Shi, Yanuo; Schweiger, Sebastian; Strelcov, Evgheni; Foglietti, Vittorio; Orgiani, Pasquale; Balestrino, Giuseppe; Kalinin, Sergei V.; Jennifer L. M. Rupp; Aruta, Carmela; et al

    2016-05-18

    Samaria-doped ceria (SDC) thin films are particularly important for energy and electronic applications such as micro-solid oxide fuel cells, electrolysers, sensors and memristors. In this paper we report a comparative study investigating ionic conductivity and surface reactions for well-grown epitaxial SDC films varying the samaria doping concentration. With increasing doping above 20 mol% of samaria, an enhancement in the defect association was observed by Raman spectroscopy. The role of such defect associates on the films` oxygen ion transport and exchange was investigated by electrochemical impedance spectroscopy and electrochemical strain microscopy (ESM). The measurements reveal that the ionic transport has amore » sharp maximum in ionic conductivity and drop in its activation energy down to 0.6 eV for 20 mol% doping. Increasing the doping concentration further up to 40 mol%, raises the activation energy substantially by a factor of two. We ascribe the sluggish transport kinetics to the "bulk" ionic-near ordering in case of the heavily doped epitaxial films. Analysis of the ESM first order reversal curve measurements indicate that these associated defects may have a beneficial role by lowering the activation of the oxygen exchange "surface" reaction for heavily doped 40 mol% of samaria. We reveal in a model experiment through a solid solution series of samaria doped ceria epitaxial films that the occurrence of associate defects in the bulk affects the surface charging state of the films to increase the exchange rates. Lastly, the implication of these findings are the design of coatings with tuned oxygen surface exchange by control of bulk associate clusters for future electro-catalytic applications.« less

  3. Preparations of PAN-based adsorbers for separation of cesium and cobalt from radioactive wastes.

    PubMed

    Nilchi, A; Atashi, H; Javid, A H; Saberi, R

    2007-05-01

    Ion-exchange adsorbers are widely used for radioisotope separation, as well as for the removal of hazardous fission products from aqueous waste prior to discharge to the environment. Inorganic exchangers are of particular interest because of their resistance to radiolytic damage and selectivity for specific fission products. Composite inorganic-organic adsorbers represent a group of inorganic ion exchangers modified by using binding organic material, polyacrylonitrile, for preparation of larger size particles with higher granular strength. At the same time, kinetics of ion exchange and sorption capacity of such composite adsorbers are not influenced by the binding polymer. The contents of active component in composite adsorber were varied over a very broad range of 5-95% of the dry weight of the composite adsorber, and tested for separation and concentration of various stimulated wastes. Three different inorganic sorbents, granular hexacyanoferrate-based ion exchanger, were developed for the removal of Cs and Co ions from waste solutions containing different complexing agents as detergents. Radiation and thermal stability studies show that these adsorbents can be used for medium-active waste treatment. PMID:17270450

  4. Preparations of PAN-based adsorbers for separation of cesium and cobalt from radioactive wastes.

    PubMed

    Nilchi, A; Atashi, H; Javid, A H; Saberi, R

    2007-05-01

    Ion-exchange adsorbers are widely used for radioisotope separation, as well as for the removal of hazardous fission products from aqueous waste prior to discharge to the environment. Inorganic exchangers are of particular interest because of their resistance to radiolytic damage and selectivity for specific fission products. Composite inorganic-organic adsorbers represent a group of inorganic ion exchangers modified by using binding organic material, polyacrylonitrile, for preparation of larger size particles with higher granular strength. At the same time, kinetics of ion exchange and sorption capacity of such composite adsorbers are not influenced by the binding polymer. The contents of active component in composite adsorber were varied over a very broad range of 5-95% of the dry weight of the composite adsorber, and tested for separation and concentration of various stimulated wastes. Three different inorganic sorbents, granular hexacyanoferrate-based ion exchanger, were developed for the removal of Cs and Co ions from waste solutions containing different complexing agents as detergents. Radiation and thermal stability studies show that these adsorbents can be used for medium-active waste treatment.

  5. Structure and Reactivity of Adsorbed Fibronectin Films on Mica

    PubMed Central

    Hull, James R.; Tamura, Glen S.; Castner, David G.

    2007-01-01

    Understanding the interactions of adsorbed fibronectin (Fn) with other biomolecules is important for many biomedical applications. Fn is found in almost all body fluids, in the extracellular matrix, and plays a fundamental role in many biological processes. This study found that the structure (conformation, orientation) and reactivity of Fn adsorbed onto mica is dependent on the Fn surface concentration. Atomic force microscopy and x-ray photoelectron spectroscopy were used to determine the surface coverage of adsorbed Fn from isolated molecules at low surface coverage to full monolayers at high surface coverage. Both methods showed that the thickness of Fn film continued to increase after the mica surface was completely covered, consistent with Fn adsorbed in a more upright conformation at the highest surface-Fn concentrations. Time-of-flight secondary ion mass spectrometry showed that relative intensities of both sulfur-containing (cystine, methionine) and hydrophobic (glycine, leucine/isoleucine) amino acids varied with changing Fn surface coverage, indicating that the conformation of adsorbed Fn depended on surface coverage. Single-molecule force spectroscopy with collagen-related peptides immobilized onto the atomic force microscope tip showed that the specific interaction force between the peptide and Fn increases with increasing Fn surface coverage. PMID:17890402

  6. Polyphosphate-enhanced production of reactive oxidants by nanoparticulate zero-valent iron and ferrous ion in the presence of oxygen: Yield and nature of oxidants.

    PubMed

    Kim, Hak-Hyeon; Lee, Hongshin; Kim, Hyung-Eun; Seo, Jiwon; Hong, Seok Won; Lee, Jeong-Yong; Lee, Changha

    2015-12-01

    The production of reactive oxidants from nanoparticulate zero-valent iron (nZVI) and ferrous ion (Fe(II)) in the presence of oxygen was greatly enhanced by the addition of tetrapolyphosphate (TPP) as an iron-chelating agent. Compared to other ligands, TPP exhibited superior activity in improving the oxidant yields. The nZVI/TPP/O2 and the Fe(II)/TPP/O2 systems showed similar oxidant yields with respect to the iron consumed, indicating that nZVI only serves as a source of Fe(II). The degradation efficacies of selected organic compounds were also similar in the two systems. It appeared that both hydroxyl radical (OH) and ferryl ion (Fe(IV)) are produced, and OH dominates at acidic pH. However, at pH > 6, little occurrence of hydroxylated oxidation products suggests that Fe(IV) is a dominant oxidant. The degradation rates of selected organic compounds by the Fe(II)/TPP/O2 system had two optimum points at pH 6 and 9, and these pH-dependent trends are likely attributed to the speciation of Fe(IV) with different reactivities.

  7. One-dimensional fossil-like γ-Fe2O3@carbon nanostructure: preparation, structural characterization and application as adsorbent for fast and selective recovery of gold ions from aqueous solution

    NASA Astrophysics Data System (ADS)

    Gunawan, Poernomo; Xiao, Wen; Hao Chua, Marcus Wen; Poh-Choo Tan, Cheryl; Ding, Jun; Zhong, Ziyi

    2016-10-01

    One-dimensional (1D) magnetic nanostructures with high thermal stability have important industrial applications, but their fabrication remains a big challenge. Herein we demonstrate a scalable approach for the preparation of stable 1D γ-Fe2O3@carbon, which is also applicable for other metal oxide-core and carbon-shell nanostructures, such as 1D TiO2@carbon. One-dimensional ferric oxyhydroxide (α-FeO(OH)) was initially prepared by a hydrothermal method, followed by carbon coating through hydrothermal treatment of the resulting metal oxide in glucose solution. After calcination in N2 gas at 500 °C and subsequent exposure to air, the initial carbon-coated 1D α-Fe2O3 was converted to 1D γ-Fe2O3@carbon, which was very stable without any observed changes even after 1.5 years of storage under ambient conditions. The materials were then used as adsorbents and found to be highly selective towards Au (III) adsorption, of which the maximum adsorption capacity is about 600 mg Au/g sorbent (1132 mg Au/g carbon). The spent sorbent containing Au after adsorption can be readily collected by applying a magnetic field due to the presence of the magnetic core, and the adsorbed Au particles are subsequently recovered after the combustion and dissolution of the sorbent. This work demonstrates not only a facile approach to the fabrication of robust 1D magnetic materials with a stable carbon shell, but also a possible cyanide-free process for the fast and selective recovery of gold from electronic waste and industrial water.

  8. One-dimensional fossil-like γ-Fe2O3@carbon nanostructure: preparation, structural characterization and application as adsorbent for fast and selective recovery of gold ions from aqueous solution.

    PubMed

    Gunawan, Poernomo; Xiao, Wen; Chua, Marcus Wen Hao; Tan, Cheryl Poh-Choo; Ding, Jun; Zhong, Ziyi

    2016-10-14

    One-dimensional (1D) magnetic nanostructures with high thermal stability have important industrial applications, but their fabrication remains a big challenge. Herein we demonstrate a scalable approach for the preparation of stable 1D γ-Fe2O3@carbon, which is also applicable for other metal oxide-core and carbon-shell nanostructures, such as 1D TiO2@carbon. One-dimensional ferric oxyhydroxide (α-FeO(OH)) was initially prepared by a hydrothermal method, followed by carbon coating through hydrothermal treatment of the resulting metal oxide in glucose solution. After calcination in N2 gas at 500 °C and subsequent exposure to air, the initial carbon-coated 1D α-Fe2O3 was converted to 1D γ-Fe2O3@carbon, which was very stable without any observed changes even after 1.5 years of storage under ambient conditions. The materials were then used as adsorbents and found to be highly selective towards Au (III) adsorption, of which the maximum adsorption capacity is about 600 mg Au/g sorbent (1132 mg Au/g carbon). The spent sorbent containing Au after adsorption can be readily collected by applying a magnetic field due to the presence of the magnetic core, and the adsorbed Au particles are subsequently recovered after the combustion and dissolution of the sorbent. This work demonstrates not only a facile approach to the fabrication of robust 1D magnetic materials with a stable carbon shell, but also a possible cyanide-free process for the fast and selective recovery of gold from electronic waste and industrial water. PMID:27585547

  9. Study of XAD-2 adsorbent for the enrichment of trace levels of phthalate esters in hydroalcoholic food beverages and analysis by gas chromatography coupled with flame ionization and ion-trap mass spectrometry detectors.

    PubMed

    Cinelli, Giuseppe; Avino, Pasquale; Notardonato, Ivan; Centola, Angela; Russo, Mario Vincenzo

    2014-03-01

    An analytical method based on solid-phase extraction (SPE) with Amberlite XAD-2 adsorbent used as stationary phase for determining phthalate esters (PAEs) in hydroalcoholic food beverages by GC-FID (and peak confirmation by GC-IT/MS) has been set up. The XAD-2 resin shows excellent properties for determining PAEs in solutions at very large alcoholic range (10-40% v/v): 500mL of hydroalcoholic solution spiked with a PAE mixture solution (20pgμL(-1) of each PAE) and containing 25gL(-1) of NaCl are passed onto a cartridge containing 500mg XAD-2 adsorbent and re-extracted for GC analysis. The effects of NaCl concentration (0, 12, 25 and 50gL(-1)) and different solvents (CS2, toluene, acetone, n-hexane, ethyl acetate) are extensively studied as well the PAE recoveries both in hydroalcoholic aqueous solutions (ranging between 94% and 103% with a Relative Standard Deviation, RSD, below 8.3) and spiked (5, 10 and 25pgμL(-1) of each PAE) real samples (between 90% and 106% with a RSD below 9.9). The correlation coefficients (R(2)) of each PAE vary between 0.9830 and 0.9950 and they are calculated in the linear range 5-100pgμL(-1). The limits of detection (LOD) in GC-FID vary between 1.21 and 2.51pgμL(-1) (RSD⩽11.1) whereas the Limits of Quantification (LOQ) range between 2.42 and 5.03pgμL(-1) (RSD⩽8.9) whereas the infra-day and inter-day repeatabilities calculated as RSD for hydroalcoholic solutions, are between 6.5% and 13.7%. PMID:24176330

  10. Atomic data and spectral analysis of carbon, nitrogen, oxygen and silicon ions observed with the International Ultraviolet Explorer

    NASA Technical Reports Server (NTRS)

    Pradhan, Anil K.

    1992-01-01

    According to the plan presented in the original proposal we have now completed most of the atomic calculations involving collision strengths and rate coefficients for electron impact excitation of C II, N III, and O IV ions. These have been reported in the first two publications appended with this report. We have now moved into the applications phase of the project with the new data being used to analyze the International Ultraviolet Explorer (IUE) observations of a variety of objects, as described in the third publication recently submitted (also appended). The analysis and interpretation of archival data will continue well into the next year with several collaborators that the PI and Co-PI are involved with. In addition, the atomic calculations on Si II have been started.

  11. Planktonic foraminiferal oxygen isotope analysis by ion microprobe technique suggests warm tropical sea surface temperatures during the Early Paleogene

    NASA Astrophysics Data System (ADS)

    Kozdon, Reinhard; Kelly, D. Clay; Kita, Noriko T.; Fournelle, John H.; Valley, John W.

    2011-09-01

    Cool tropical sea surface temperatures (SSTs) are reported for warm Paleogene greenhouse climates based on the δ18O of planktonic foraminiferal tests. These results are difficult to reconcile with models of greenhouse gas-forced climate. It has been suggested that this "cool tropics paradox" arises from postdepositional alteration of foraminiferal calcite, yielding erroneously high δ18O values. Recrystallization of foraminiferal tests is cryptic and difficult to quantify, and the compilation of robust δ18O records from moderately altered material remains challenging. Scanning electron microscopy of planktonic foraminiferal chamber-wall cross sections reveals that the basal area of muricae, pustular outgrowths on the chamber walls of species belonging to the genus Morozovella, contain no mural pores and may be less susceptible to postdepositional alteration. We analyzed the δ18O in muricae bases of morozovellids from the central Pacific (Ocean Drilling Program Site 865) by ion microprobe using 10 μm pits with an analytical reproducibility of ±0.34‰ (2 standard deviations). In situ measurements of δ18O in these domains yield consistently lower values than those published for conventional multispecimen analyses. Assuming that the original δ18O is largely preserved in the basal areas of muricae, this new δ18O record indicates Early Paleogene (˜49-56 Ma) tropical SSTs in the central Pacific were 4°-8°C higher than inferred from the previously published δ18O record and that SSTs reached at least ˜33°C during the Paleocene-Eocene thermal maximum. This study demonstrates the utility of ion microprobe analysis for generating more reliable paleoclimate records from moderately altered foraminiferal tests preserved in deep-sea sediments.

  12. Correlation of structure and ion conduction in La{sub 2−x}Y{sub x}Mo{sub 2}O{sub 9} (0 ≤ x ≤ 0.2) oxygen ion conductors

    SciTech Connect

    Paul, T.; Ghosh, A.

    2015-06-21

    Correlation of structure and ion conduction of La{sub 2−x}Y{sub x}Mo{sub 2}O{sub 9} (0 ≤ x ≤ 0.2) has been investigated. The cubic symmetry with space group P2{sub 1}3 and other structural parameters are obtained from Rietveld refinement of X-ray diffraction patterns of Y doped samples. The average lanthanum-oxygen and molybdenum-oxygen distances are obtained from the electron density contour plot. The transmission electron microscopic study confirms the cubic nature of the samples and also provides an estimate of thickness of the grain boundary. The scanning transmission electron microscope energy dispersive spectrometer mapping confirms the different orientations of grains. The composition dependence of the ionic conductivity has been correlated with that of O2 and O3 site occupancies in the [O1La{sub 3}Mo] antitetrahedral unit. The different vibrational modes in the low frequency region due to vibration of Mo-O bands are confirmed from the analysis of FTIR and Raman spectra. The full widths at half maximum of most of the Mo-O bands are found to be independent of Y doping. Additionally, the shifts in the position of Raman bands are correlated with unit cell parameter using Grüneisen constant.

  13. Oxidation of Fe(110) in oxygen gas at 400 °C

    NASA Astrophysics Data System (ADS)

    Soldemo, Markus; Lundgren, Edvin; Weissenrieder, Jonas

    2016-02-01

    The initial oxidation of Fe(110) in oxygen gas at 400 °C beyond initial adsorbate structures has been studied using X-ray photoelectron spectroscopy, X-ray absorption spectroscopy, low-energy electron diffraction, and scanning tunneling microscopy (STM). Formation of several ordered phases of surface oxides is observed at oxygen coverages between approximately 2.3 and 3.5 oxygen atoms/Fe(110) surface atom. Initially, a FeO(111)-like film is formed with a parallelogram-shaped moiré pattern. It has two mirror domains that are formed symmetrically around the growth direction of a zigzag-shaped adsorbate structure. With increased local oxygen coverage, the moiré structure transforms into a ball-shaped form. Both these moiré structures have equal atomic stacking at the surface and equal apparent height in STM, suggesting oxygen ions diffusing into the film upon oxidation and that the oxide growth takes place at the iron-iron oxide interface. The FeO(111)-like film turns into a Fe3O4(111)-like film with a triangular bistable surface termination as the oxidation proceeds further. The FeO(111)-like film growth proceeds according to the Frank-van der Merwe mechanism while the Fe3O4(111)-like film grows according to the Stranski-Krastanov mechanism.

  14. A cellular automaton model examining the effects of oxygen, hydrogen ions and lactate on early tumour growth.

    PubMed

    Al-Husari, Maymona; Murdoch, Craig; Webb, Steven D

    2014-10-01

    Some tumours are known to exhibit an extracellular pH that is more acidic than the intracellular, creating a 'reversed pH gradient' across the cell membrane and this has been shown to affect their invasive and metastatic potential. Tumour hypoxia also plays an important role in tumour development and has been directly linked to both tumour morphology and aggressiveness. In this paper, we present a hybrid mathematical model of intracellular pH regulation that examines the effect of oxygen and pH on tumour growth and morphology. In particular, we investigate the impact of pH regulatory mechanisms on the cellular pH gradient and tumour morphology. Analysis of the model shows that: low activity of the Na+/H+ exchanger or a high rate of anaerobic glycolysis can give rise to a "fingering" tumour morphology; and a high activity of the lactate/H+ symporter can result in a reversed transmembrane pH gradient across a large portion of the tumour mass. Also, the reversed pH gradient is spatially heterogeneous within the tumour, with a normal pH gradient observed within an intermediate growth layer within the spheroid. We also include a fractal dimension analysis of the simulated tumour contours, in which we compare the fractal dimensions of the simulated tumour surfaces with those found experimentally via photomicrographs.

  15. Biodegradable metal adsorbent synthesized by graft polymerization onto nonwoven cotton fabric

    NASA Astrophysics Data System (ADS)

    Sekine, Ayako; Seko, Noriaki; Tamada, Masao; Suzuki, Yoshio

    2010-01-01

    A fibrous adsorbent for Hg ions was synthesized by radiation-induced emulsion graft polymerization of glycidyl methacrylate (GMA) onto a nonwoven cotton fabric and subsequent chemical modification. The optimal pre-irradiation dose for initiation of the graft polymerization of GMA, which minimized the effects of radiation damage on the mechanical strength of the nonwoven cotton fabric, was found to be 10 kGy. The GMA-grafted nonwoven cotton fabric was subsequently modified with ethylenediamine (EDA) or diethylenetriamine (DETA) to obtain a Hg adsorbent. The resulting amine-type adsorbents were evaluated for batch and continuous adsorption of Hg. In batch adsorption, the distribution coefficients of Hg reached 1.9×10 5 and 1.0×10 5 for EDA- and DETA-type adsorbents, respectively. A column packed with EDA-type adsorbent removed Hg from 1.8 ppm Hg solution at a space velocity of 100 h -1, which corresponds to 16,000 times the volume of the packed adsorbent. The adsorbed Hg on the EDA-type adsorbent could be completely eluted by 1 M HCl solution. A microbial oxidative degradation test revealed that the EDA-type adsorbent is biodegradable.

  16. Assessment of grain-scale homogeneity and equilibration of carbon and oxygen isotope compositions of minerals in carbonate-bearing metamorphic rocks by ion microprobe

    NASA Astrophysics Data System (ADS)

    Ferry, John M.; Ushikubo, Takayuki; Kita, Noriko T.; Valley, John W.

    2010-11-01

    Nineteen samples of metamorphosed carbonate-bearing rocks were analyzed for carbon and oxygen isotope ratios by ion microprobe with a ˜5-15 μm spot, three from a regional terrain and 16 from five different contact aureoles. Contact metamorphic rocks further represent four groups: calc-silicate marble and hornfels (6), brucite marble (2), samples that contain a reaction front (4), and samples with a pervasive distribution of reactants and products of a decarbonation reaction (4). The average spot-to-spot reproducibility of standard calcite analyses is ±0.37‰ (2 standard deviations, SD) for δ 18O and ±0.71‰ for δ 13C. Ten or more measurements of a mineral in a sample that has uniform isotope composition within error of measurement can routinely return a weighted mean with a 95% confidence interval of 0.09-0.16‰ for δ 18O and 0.10-0.29‰ for δ 13C. Using a difference of >6SD as the criterion, only four of 19 analyzed samples exhibit significant intracrystalline and/or intercrystalline inhomogeneity in δ 13C at the 100-500 μm scale, with differences within individual grains up to 3.7‰. Measurements are consistent with carbon isotope exchange equilibrium between calcite and dolomite in five of six analyzed samples at the same scale. Because of relatively slow carbon isotope diffusion in calcite and dolomite, differences in δ 13C can survive intracrystalline homogenization by diffusion during cooling after peak metamorphism and likely represent the effects of prograde decarbonation and infiltration. All but 2 of 11 analyzed samples exhibit intracrystalline differences in δ 18O (up to 9.4‰), intercrystalline inhomogeneity in δ 18O (up to 12.5‰), and/or disequilibrium oxygen isotope fractionations among calcite-dolomite, calcite-quartz, and calcite-forsterite pairs at the 100-500 μm scale. Inhomogeneities in δ 18O and δ 13C are poorly correlated with only a single mineral (dolomite) in a single sample exhibiting both. Because of relatively

  17. Solar Wind Influence on the Oxygen Content of Ion Outflow in the High Altitude Polar Cap During Solar Minimum Conditions

    NASA Technical Reports Server (NTRS)

    Elliott, Heather A.; Comfort, Richard H.; Craven, Paul D.; Chandler, Michael O.; Moore, Thomas E.

    2000-01-01

    We correlate solar wind and IMF properties with the properties of O(+) and H(+) in the polar cap in early 1996 during solar minimum conditions at altitudes between 5.5 and 8.9 Re geocentric using the Thermal Ion Dynamics Experiment (TIDE) on the POLAR satellite. Throughout the high altitude polar cap, we observe H(+) to be more abundant than O(+). H(+) is a significant fraction of both the ionosphere and the solar wind, and O(+) is not a significant species in the solar wind. O(+) is the major species in the ionosphere so the faction of O(+) present in the magnetosphere is commonly used as a measure of the ionospheric contribution to the magnetosphere. For these reasons, 0+ is of primary interest in this study. We observe O(+) to be most abundant at lower latitudes when the solar wind speed is low (and low Kp), and at higher solar wind speeds (and high Kp) O(+) is observed across most of the polar cap. We also find that O(+) density and parallel flux are well organized by solar wind dynamic pressure; they both increase with solar wind dynamic pressure. H(+) is not as highly correlated with solar wind and IMF parameters, but H(+) density and parallel flux have some negative correlation with IMF By, and some positive correlation with VswBIMF. In this solar minimum data set, H(+) is dominant so that contributions of this plasma to the plasma sheet would have a very low O(+) to H(+) ratio.

  18. Electron emission in ionization of He and Ne by fast dressed oxygen ions and projectile-charge-state dependence

    NASA Astrophysics Data System (ADS)

    Biswas, Shubhadeep; Kasthurirangan, S.; Misra, D.; Monti, J. M.; Rivarola, R. D.; Fainstein, P. D.; Tribedi, L. C.

    2015-02-01

    The double-differential cross sections (DDCS) of low-energy electrons emitted at forward, backward, and perpendicular directions are reported for collisions of 3.75 MeV/u Oq + (q =5 , 6, 7, 8) projectiles with He and Ne targets. The measured DDCS are found to be deviating from the q2 dependence throughout the entire energy region. The effect of projectile electrons, for the dressed ions, as a function of the impact parameter is clearly noticeable for large as well as low-impact parameter collisions. We also present a theoretical calculation based on the prior form of the continuum distorted wave-eikonal initial state approximation, in which the projectile-active electron interaction is modeled with the Green-Sellin-Zachor potential. This particular representation of the potential has been proven to give good qualitative results for projectiles with residual electrons. In addition to the total DDCS, the individual contributions from target ionization, projectile electron loss, and simultaneous ionization processes are also calculated. The total DDCS obtained from these calculations are shown to be in excellent agreement with the experimental observations.

  19. Ion bombardment effects on ZnO nanowires during plasma treatment

    NASA Astrophysics Data System (ADS)

    Ra, H.-W.; Choi, K. S.; Ok, C. W.; Jo, S. Y.; Bai, K. H.; Im, Y. H.

    2008-07-01

    We present the effects of ion bombardment on ZnO nanowires caused by their exposure to an Ar inductively coupled plasma. The conductivity of the individual ZnO nanowire was increased in up to 3 orders of magnitude due to increase in both carrier concentration and mobility, with a substantial negative shift in the threshold gate voltage also being observed. The drastic changes in the electrical properties were attributed to the decrease in species adsorbed on the surface, as well as to the increase in oxygen vacancies near the surface caused by ion bombardment.

  20. Visual detection of trace copper ions based on copper-catalyzed reaction of ascorbic acid with oxygen

    NASA Astrophysics Data System (ADS)

    Hou, Xin Yan; Chen, Shu; Shun, Lian Ju; Zhao, Yi Ni; Zhang, Zhi Wu; Long, Yun Fei; Zhu, Li

    2015-10-01

    A visual detection method for trace Cu2+ in aqueous solutions using triangular silver nanoplates (abbreviated as TAgNPs) as the probe was developed. The method is based on that TAgNPs could be corroded in sodium thiosulfate (Na2S2O3) solutions. The absorption spectrum of TAgNPs solution changed when it is corroded by Na2S2O3. The reaction of oxygen with ascorbic acid (Vc) in the presence of a low concentration of Cu2+ generates hydrogen peroxide that reacts with Na2S2O3, which leads the concentration of Na2S2O3 in the solution to be decreased. Therefore, the reaction between TAgNPs and the reacted mixture of Na2S2O3/Vc/Cu2+ was prevented efficiently. When the Na2S2O3 concentration and reaction time are constant, the decrease in the concentration of Na2S2O3 is directly proportional to the Cu2+ concentration. Thus, morphology, color, and maximum absorption wavelength of TAgNPs changed with the change of Cu2+ concentration. The changed maximum absorption wavelength of TAgNPs (Δλ) is proportional to Cu2+ concentration in the range from 7.5 × 10-9 to 5.0 × 10-7 M with a correlation coefficient of r = 0.9956. Moreover, color change of TAgNP solution was observed clearly over a Cu2+ concentration range from 7.5 × 10-8 to 5.0 × 10-7 M. This method has been used to detect the Cu2+ content of a human hair sample, and the result is in agreement with that obtained by the atomic absorption spectroscopy (AAS) method.

  1. EFFECT OF MOLECULAR OXYGEN ON THE SCALEUP OF GAC ADSORBERS

    EPA Science Inventory

    A rapid small-scale column test (RSSCT), designed according to the assumption of no dependency of the intraparticle surface diffusion coefficient on the activated carbon particle size, was able to accurately predict breakthrough of three volatile organic chemicals as well as back...

  2. The role of strain and structure on oxygen ion conduction in nanoscale zirconia and ceria thin films

    NASA Astrophysics Data System (ADS)

    Jiang, Jun

    were decreased 3 - 7 times. YSZ thin films deposited on Al2O3 obtained a stable epitaxial growth along [110] (111)YSZ//[1010] (0001)Al2O3. By tailoring the thickness of YSZ thin film on Al2O3 from 100 nm to 6 nm, the lattice strain can be increased from nearly 1% to 2%. The corresponding conductivity increased by about 1 order of magnitude and the activation energy decreased from 0.99 eV to 0.79 eV. Ion cleaning of the MgO substrate surface was found to change the YSZ thin films' texture without large change to the conductivity, while ion cleaning of the Al2O3 substrate surface decreased the crystallinity without changing the texture and reduced the ionic conductivity of YSZ thin films by a factor of 4. Thus, crystallinity not texture was found to determine the ionic conductivity. In addition, a post annealing with a temperature as high as 1000 °C was able to increase the crystallinity of YSZ thin films therefore increasing the conductivity by a factor of 2. Gadolinia doped ceria (GDC) thin films deposited on MgO were randomly oriented along multi axes, suggesting a polycrystalline structure. While, on Al2O3, GDC thin films' growth became stable only oriented in (111) orientation, just like YSZ thin films on Al2O 3. In the thickness range of 15 nm - 173 nm, the maximum conductivity of GDC thin films was obtained at the thickness of 81 nm. Interestingly, as GDC thin films' thickness increased above 100 nm, the electrical properties changed from a bulk-like conduction to a grain boundary-like conduction.

  3. Assembling metal oxide nanocrystals into dense, hollow, porous nanoparticles for lithium-ion and lithium-oxygen battery application.

    PubMed

    Ming, Jun; Wu, Yingqiang; Park, Jin-Bum; Lee, Joong Kee; Zhao, Fengyu; Sun, Yang-Kook

    2013-11-01

    New dense hollow porous (DHP) metal oxide nanoparticles that are smaller than 100 nm and composed of Co3O4, FeOx, NiO and MnOx were prepared by densely assembling metal oxide nanocrystals based on the hard-template method using a carbon colloid as a sacrificial core. These nanoparticles are quite different from the traditional particles as their hollow interior originates from the stacking of nanocrystals rather than a spherical shell. The DHP nanoparticles preserve the intriguing properties of nanocrystals and possess desirable surface area and pore volume that enhance the active surface, which ultimately benefits applications such as lithium-ion batteries. The DHP Co3O4 nanoparticles demonstrated an enhanced capacity of 1168 mA h g(-1) at 100 mA g(-1)vs. 590 mA h g(-1) of powders and stable cycling performance greater than 250 cycles when used as an anode material. Most importantly, the electrochemical performance of DHP Co3O4 nanoparticles in a lithium-O2 battery was also investigated for the first time. A low charge potential of ∼4.0 V, a high discharge voltage near 2.74 V and a long cycle ability greater than 100 cycles at a delivered capacity of 2000 mA h g(-1) (current density, 200 mA g(-1)) were observed. The performances were considerably improved compared to recent results of mesoporous Co3O4, Co3O4 nanoparticles and a composite of Co3O4/RGO and Co3O4/Pd. Therefore, it would be promising to investigate such properties of DHP nanoparticles or other hollow metal (oxide) particles for the popular lithium-air battery.

  4. Supercritical fluid regeneration of adsorbents

    NASA Astrophysics Data System (ADS)

    Defilippi, R. P.; Robey, R. J.

    1983-05-01

    The results of a program to perform studies supercritical (fluid) carbon dioxide (SCF CO2) regeneration of adsorbents, using samples of industrial wastewaters from manufacturing pesticides and synthetic solution, and to estimate the economics of the specific wastewater treatment regenerations, based on test data are given. Processing costs for regenerating granular activated carbon GAC) for treating industrial wastewaters depend on stream properties and regeneration throughput.

  5. Structural characterization of adsorbed helical and beta-sheet peptides

    NASA Astrophysics Data System (ADS)

    Samuel, Newton Thangadurai

    Adsorbed peptides on surfaces have potential applications in the fields of biomaterials, tissue engineering, peptide microarrays and nanobiotechnology. The surface region, the "biomolecular interface" between a material and the biological environment, plays a crucial role in these applications. As a result, characterization of adsorbed peptide structure, especially with respect to identity, concentration, spatial distribution, conformation and orientation, is important. The present research employs NEXAFS (near-edge X-ray absorption fine structure spectroscopy) and SFG (sum frequency generation spectroscopy) to provide information about the adsorbed peptide structure. Soft X-ray NEXAFS is a synchrotron-based technique which typically utilizes polarized X-rays to interrogate surfaces under ultra-high vacuum conditions. SFG is a non-linear optical technique which utilizes a combination of a fixed visible and a tunable infrared laser beams to generate a surface-vibrational spectrum of surface species. SFG has the added advantage of being able to directly analyze the surface-structure at the solid-liquid interface. The main goals of the present research were twofold: characterize the structure of adsorbed peptides (1) ex situ using soft X-ray NEXAFS, and (2) in situ using non-linear laser spectroscopy (SFG). Achieving the former goal involved first developing a comprehensive characterization of the carbon, nitrogen and oxygen k-edge NEXAFS spectra for amino acids, and then using a series of helical and beta-sheet peptides to demonstrate the sensitivity of polarization-dependent NEXAFS to secondary structure of adsorbed peptides. Characterizing the structure of adsorbed peptides in situ using SFG involved developing a model system to probe the solid-liquid interface in situ; demonstrating the ability to probe the molecular interactions and adsorbed secondary structure; following the time-dependent ordering of the adsorbed peptides; and establishing the ability to obtain

  6. Laboratory Measurements of Oxygen Gas Release from Basaltic Minerals Exposed to UV- Radiation: Implications for the Viking Gas Exchange Experiments

    NASA Astrophysics Data System (ADS)

    Hurowitz, J. A.; Yen, A. S.

    2007-12-01

    The biology experiments onboard the Viking Landers determined that the Martian soils at Chryse and Utopia Planitia contain an unknown chemical compound of a highly oxidizing nature. The Gas Exchange Experiments (GEx) demonstrated that the humidification of a 1-cc Martian soil sample resulted in the production of as much as 790 nanomoles of oxygen gas. Yen et al. (2000) have provided experimental evidence that superoxide radicals can be generated on plagioclase feldspar (labradorite) grain surfaces by exposure to ultraviolet (UV) light in the presence of oxygen gas. Adsorbed superoxide radicals are thought to react readily with water vapor, and produce oxygen gas in quantities sufficient to explain the Viking GEx results. Direct evidence for the formation of oxygen gas, however, was not provided in the experiments of Yen et al (2000). Accordingly, the motivation of this study is to determine whether superoxide radicals adsorbed on labradorite surfaces are capable of producing oxygen gas upon exposure to water vapor. We have constructed an experimental apparatus that is capable of monitoring oxygen gas release from basaltic mineral powders that have been exposed to UV-radiation under Martian atmospheric pressure conditions. The apparatus consists of a stainless-steel vacuum chamber with a UV- transparent window where sample radiation exposures are performed. The vacuum chamber has multiple valved ports for injection of gases and water vapor. The vacuum chamber is connected via a precision leak valve to a quadrupole mass spectrometer, which measures changes in the composition of the headspace gases over our mineral samples. We will report on the results of our experiments, which are aimed at detecting and quantifying oxygen gas release from UV-exposed basaltic mineral samples using this new experimental facility. These results will further constrain whether superoxide ions adsorbed on mineral surfaces provide a viable explanation for the Viking GEx results, which have

  7. Method And Apparatus For Regenerating Nox Adsorbers

    DOEpatents

    Driscoll, J. Joshua; Endicott, Dennis L.; Faulkner, Stephen A.; Verkiel, Maarten

    2006-03-28

    Methods and apparatuses for regenerating a NOx adsorber coupled with an exhaust of an engine. An actuator drives a throttle valve to a first position when regeneration of the NOx adsorber is desired. The first position is a position that causes the regeneration of the NOx adsorber. An actuator drives the throttle valve to a second position while regeneration of the NOx adsorber is still desired. The second position being a position that is more open than the first position and operable to regenerate a NOx adsorber.

  8. Acute exposure to 930 MHz CW electromagnetic radiation in vitro affects reactive oxygen species level in rat lymphocytes treated by iron ions.

    PubMed

    Zmyślony, Marek; Politanski, Piotr; Rajkowska, Elzbieta; Szymczak, Wieslaw; Jajte, Jolanta

    2004-07-01

    The aim of this study was to test the hypothesis that the 930 MHz continuous wave (CW) electromagnetic field, which is the carrier of signals emitted by cellular phones, affects the reactive oxygen species (ROS) level in living cells. Rat lymphocytes were used in the experiments. A portion of the lymphocytes was treated with iron ions to induce oxidative processes. Exposures to electromagnetic radiation (power density 5 W/m2, theoretical calculated SAR = 1.5 W/kg) were performed within a GTEM cell. Intracellular ROS were measured by the fluorescent probe dichlorofluorescin diacetate (DCF-DA). The results show that acute (5 and 15 min) exposure does not affect the number of produced ROS. If, however, FeCl2 with final concentration 10 microg/ml was added to the lymphocyte suspensions to stimulate ROS production, after both durations of exposure, the magnitude of fluorescence (ROS level during the experiment) was significantly greater in the exposed lymphocytes. The character of the changes in the number of free radicals observed in our experiments was qualitatively compatible with the theoretical prediction from the model of electromagnetic radiation effect on radical pairs. PMID:15197754

  9. Durability to oxygen reactive ion etching enhanced by addition of synthesized bis(trimethylsilyl)phenyl-containing (meth)acrylates in ultraviolet nanoimprint lithography

    NASA Astrophysics Data System (ADS)

    Ito, Shunya; Sato, Hiroki; Tasaki, Yuhei; Watanuki, Kimihito; Nemoto, Nobukatsu; Nakagawa, Masaru

    2016-06-01

    We investigated the selection of bis(trimethylsilyl)phenyl-containing (meth)acrylates as additives to improve the durability to oxygen reactive ion etching (O2 RIE) of sub-50 nm imprint resist patterns suitable for bubble-defect-free UV nanoimprinting with a readily condensable gas. 2,5-Bis(2-acryloyloxyethoxy)-1,4-bis(trimethylsilyl)benzene, which has a diacrylate chemical structure similar to that of glycerol 1,3-diglycerolate diacrylate used as a base monomer, and 3-(2-methacryloyloxyethoxy)-1-(hydroxylethoxy)-2-propoxy-3,5-bis(trimethylsilyl)benzene, which has a hydroxy group similar to the base monomer, were synthesized taking into consideration the Ohnishi and ring parameters, and the oxidization of the trimethylsilyl moiety to inorganic species during O2 RIE. The addition of the latter liquid additive to the base monomer decreased etching rate owing to the good miscibility of the additive in the base monomer, while the addition of the former crystalline additive caused phase separation after UV nanoimprinting. The latter additive worked as a compatibilizer to the former additive, which is preferred for etching durability improvement. The coexistence of the additives enabled the fabrication of a 45 nm line-and-space resist pattern by UV nanoimprinting, and its residual layer could be removed by O2 RIE.

  10. Unusual Rectifying Response of Nanojunctions Using Randomly Oriented Nanorods (RON) of ZnO Irradiated with 80-MeV Oxygen Ions

    NASA Astrophysics Data System (ADS)

    Bayan, Sayan; Mohanta, Dambarudhar

    2012-07-01

    The present work highlights the improved Schottky behavior of Ag/ZnO nanojunctions which make use of unirradiated and 80-MeV oxygen ion (O6+) irradiated randomly oriented ZnO nanorods. While leakage current is apparently low, the rectifying nature of the nanojunctions was clearly evident from room-temperature current-voltage ( I- V) measurements. In case of use of irradiated nanorods, the Schottky barrier height ( ϕ B) of the Ag/ZnO nanojunctions was found to be enhanced from 0.78 eV to 0.95 eV along with decrease of the ideality factor ( η) from 17.7 to 6.9. This is ascribed to reorganization and modification of the native defect states via creation and annihilation events as revealed by photoluminescence spectroscopy. The fluence-dependent variation of ϕ B and η was assigned to competition among donor and acceptor types of defects. The current transport mechanism of the Schottky contacts was found to be dominated by trap-assisted recombination tunneling and space charge-limited conduction in the mobility and ballistic regime.

  11. B and N isolate-doped graphitic carbon nanosheets from nitrogen-containing ion-exchanged resins for enhanced oxygen reduction

    NASA Astrophysics Data System (ADS)

    Wang, Lei; Yu, Peng; Zhao, Lu; Tian, Chungui; Zhao, Dongdong; Zhou, Wei; Yin, Jie; Wang, Ruihong; Fu, Honggang

    2014-06-01

    B,N-codoped carbon nanostructures (BNCS) can serve as alternative low-cost metal-free electrocatalysts for oxygen reduction reactions (ORR). However, the compensation effect between the p- (B atoms) and n-type (N atoms) dopants would make the covalent boron-nitride (BN) easily formed during the synthesis of BNCS, leading to a unsatisfactory ORR activity. Therefore, it has been challenging to develop facile and rapid synthetic strategies for highly active BNCS without forming the direct covalent BN. Here, a facile method is developed to prepare B and N isolate-doped graphitic nanosheets (BNGS) by using iron species for saving N element and simultaneous doping the B element from nitrogen-containing ion-exchanged resins (NR). The resulting BNGS exhibits much more onset potential (Eonset) compared with the B-doped graphitic carbon nanosheets (BGS), N-doped graphitic carbon nanosheets (NGS), as well as B,N-codoped disorder carbon (BNC). Moreover, the BNGS shows well methanol tolerance propery and excellent stability (a minimal loss of activity after 5,000 potential cycles) compared to that of commercial Pt/C catalyst. The goog performance for BNGS towards ORR is attributed to the synergistic effect between B and N, and the well electrons transport property of graphitic carbon in BNGS.

  12. Acute exposure to 930 MHz CW electromagnetic radiation in vitro affects reactive oxygen species level in rat lymphocytes treated by iron ions.

    PubMed

    Zmyślony, Marek; Politanski, Piotr; Rajkowska, Elzbieta; Szymczak, Wieslaw; Jajte, Jolanta

    2004-07-01

    The aim of this study was to test the hypothesis that the 930 MHz continuous wave (CW) electromagnetic field, which is the carrier of signals emitted by cellular phones, affects the reactive oxygen species (ROS) level in living cells. Rat lymphocytes were used in the experiments. A portion of the lymphocytes was treated with iron ions to induce oxidative processes. Exposures to electromagnetic radiation (power density 5 W/m2, theoretical calculated SAR = 1.5 W/kg) were performed within a GTEM cell. Intracellular ROS were measured by the fluorescent probe dichlorofluorescin diacetate (DCF-DA). The results show that acute (5 and 15 min) exposure does not affect the number of produced ROS. If, however, FeCl2 with final concentration 10 microg/ml was added to the lymphocyte suspensions to stimulate ROS production, after both durations of exposure, the magnitude of fluorescence (ROS level during the experiment) was significantly greater in the exposed lymphocytes. The character of the changes in the number of free radicals observed in our experiments was qualitatively compatible with the theoretical prediction from the model of electromagnetic radiation effect on radical pairs.

  13. B and N isolate-doped graphitic carbon nanosheets from nitrogen-containing ion-exchanged resins for enhanced oxygen reduction

    PubMed Central

    Wang, Lei; Yu, Peng; Zhao, Lu; Tian, Chungui; Zhao, Dongdong; Zhou, Wei; Yin, Jie; Wang, Ruihong; Fu, Honggang

    2014-01-01

    B,N-codoped carbon nanostructures (BNCS) can serve as alternative low-cost metal-free electrocatalysts for oxygen reduction reactions (ORR). However, the compensation effect between the p- (B atoms) and n-type (N atoms) dopants would make the covalent boron-nitride (BN) easily formed during the synthesis of BNCS, leading to a unsatisfactory ORR activity. Therefore, it has been challenging to develop facile and rapid synthetic strategies for highly active BNCS without forming the direct covalent BN. Here, a facile method is developed to prepare B and N isolate-doped graphitic nanosheets (BNGS) by using iron species for saving N element and simultaneous doping the B element from nitrogen-containing ion-exchanged resins (NR). The resulting BNGS exhibits much more onset potential (Eonset) compared with the B-doped graphitic carbon nanosheets (BGS), N-doped graphitic carbon nanosheets (NGS), as well as B,N-codoped disorder carbon (BNC). Moreover, the BNGS shows well methanol tolerance propery and excellent stability (a minimal loss of activity after 5,000 potential cycles) compared to that of commercial Pt/C catalyst. The goog performance for BNGS towards ORR is attributed to the synergistic effect between B and N, and the well electrons transport property of graphitic carbon in BNGS. PMID:24898033

  14. [The role of reactive oxygen species and calcium ions in the implementation of the stress-protective effect of brassinosteroids on plant cells].

    PubMed

    Kolupaev, Iu E; Vaĭner, A A; Iastreb, T O; Oboznyĭ, A I; Khripach, V A

    2014-01-01

    The effect of the brassinosteroids (BS) 24-epibrassiniolide and 24-epicastasterone on the thermoresistance of wheat coleoptile (Triticum aestivum L.) and their generation of the superoxide anion radical and antioxidant enzymes activity were investigated. The treatment of coleoptiles with 10 nM solutions of BS caused a transient increase in O2·- generation and a subsequent increase in the activity of superoxide dismutase and catalase and an improvement in heat resistance. Pretreatment of coleoptiles with the NADPH oxidase inhibitor imidazole leveled the increase in production of the superoxide anion radical and prevented an increase in the activity of antioxidant enzymes and the development of cell thermostability. The investigated effects of BS were also depressed by the pretreatment of coleoptile segments with extracellular calcium chelator EGTA and inhibitor of ADP-ribosyl cyclase nicotinamide. A conclusion was made about the participation of calcium ions and reactive oxygen species generated by the action of NADPH oxidase in the implementation of the stress-protective effect of the BS in the cells of wheat coleoptile.

  15. Hybrid of porous cobalt oxide nanospheres and nitrogen-doped graphene for applications in lithium-ion batteries and oxygen reduction reaction

    NASA Astrophysics Data System (ADS)

    Zhang, Mengmeng; Li, Rong; Chang, Xiaoxuan; Xue, Chao; Gou, Xinglong

    2015-09-01

    A new single-source precursor has been developed from the hydrothermal reaction of graphite oxide (GO), melamine resin (MR) monomers, and CoCl2 to prepare a sandwich-like hybrid of ultrathin nitrogen-doped graphene (NG) sheets and porous Co3O4 nanospheres (Co3O4/NG). This unique structure endows the Co3O4/NG hybrid with large surface area and enhanced electrochemical performances as both anode material for Li-ion batteries and electrocatalyst for oxygen reduction reaction (ORR). As an anode material, it exhibits high reversible capacity, excellent cycling stability and rate performance (1236 and 489 mAh g-1 over 200 cycles at 0.1C and 2C, respectively; 371 mAh g-1 at 5C). As an ORR electrocatalyst, it shows superior catalytic activity and high selectivity for the four-electron reduction pathway compared to the bare Co3O4 and NG alone. Moreover, the Co3O4/NG hybrid is insensitive to methanol, and is much more stable than Pt/C catalyst over long term operation.

  16. Applications and limits of theoretical adsorption models for predicting the adsorption properties of adsorbents.

    PubMed

    Park, Hyun Ju; Nguyen, Duc Canh; Na, Choon-Ki; Kim, Chung-il

    2015-01-01

    The objective of this study is to evaluate the applicability of adsorption models for predicting the properties of adsorbents. The kinetics of the adsorption of NO3- ions on a PP-g-AA-Am non-woven fabric have been investigated under equilibrium conditions in both batch and fixed bed column processes. The adsorption equilibrium experiments in the batch process were carried out under different adsorbate concentration and adsorbent dosage conditions and the results were analyzed using adsorption isotherm models, energy models, and kinetic models. The results of the analysis indicate that the adsorption occurring at a fixed adsorbate concentration with a varying adsorbent dosage occur more easily compared to those under a fixed adsorbent dosage with a varying adsorbate concentration. In the second part of the study, the experimental data obtained using fixed bed columns were fit to Bed Depth Service Time, Bohart-Adams, Clark, and Wolborska models, to predict the breakthrough curves and determine the column kinetic parameters. The adsorption properties of the NO3- ions on the PP-g-AA-Am non-woven fabric were differently described by different models for both the batch and fixed bed column process. Therefore, it appears reasonable to assume that the adsorption properties were dominated by multiple mechanisms, depending on the experimental conditions.

  17. Selective cesium removal from radioactive liquid waste by crown ether immobilized new class conjugate adsorbent.

    PubMed

    Awual, Md Rabiul; Yaita, Tsuyoshi; Taguchi, Tomitsugu; Shiwaku, Hideaki; Suzuki, Shinichi; Okamoto, Yoshihiro

    2014-08-15

    Conjugate materials can provide chemical functionality, enabling an assembly of the ligand complexation ability to metal ions that are important for applications, such as separation and removal devices. In this study, we developed ligand immobilized conjugate adsorbent for selective cesium (Cs) removal from wastewater. The adsorbent was synthesized by direct immobilization of dibenzo-24-crown-8 ether onto inorganic mesoporous silica. The effective parameters such as solution pH, contact time, initial Cs concentration and ionic strength of Na and K ion concentrations were evaluated and optimized systematically. This adsorbent was exhibited the high surface area-to-volume ratios and uniformly shaped pores in case cavities, and its active sites kept open functionality to taking up Cs. The obtained results revealed that adsorbent had higher selectivity toward Cs even in the presence of a high concentration of Na and K and this is probably due to the Cs-π interaction of the benzene ring. The proposed adsorbent was successfully applied for radioactive Cs removal to be used as the potential candidate in Fukushima nuclear wastewater treatment. The adsorbed Cs was eluted with suitable eluent and simultaneously regenerated into the initial form for the next removal operation after rinsing with water. The adsorbent retained functionality despite several cycles during sorption-elution-regeneration operations.

  18. Extraction of palladium from acidic solutions with the use of carbon adsorbents

    SciTech Connect

    O.N. Kononova; N.G. Goryaeva; N.B. Dostovalova; S.V. Kachin; A.G. Kholmogorov

    2007-08-15

    We studied the sorption of palladium(II) on LKAU-4, LKAU-7, and BAU carbon adsorbents from model hydrochloric acid solutions and the solutions of spent palladium-containing catalysts. It was found that sorbents based on charcoal (BAU) and anthracite (LKAU-4) were characterized by high sorption capacities for palladium. The kinetics of the saturation of carbon adsorbents with palladium(II) ions was studied, and it was found that more than 60% of the initial amount of Pd(II) was recovered in a 1-h contact of an adsorbent with a model solution. This value for the solutions of spent catalysts was higher than 35%.

  19. Hydraulic properties of adsorbed water films in unsaturated porous media

    SciTech Connect

    Tokunaga, Tetsu K.

    2009-03-01

    Adsorbed water films strongly influence residual water saturations and hydraulic conductivities in porous media at low saturations. Hydraulic properties of adsorbed water films in unsaturated porous media were investigated through combining Langmuir's film model with scaling analysis, without use of any adjustable parameters. Diffuse double layer influences are predicted to be important through the strong dependence of adsorbed water film thickness (f) on matric potential ({Psi}) and ion charge (z). Film thickness, film velocity, and unsaturated hydraulic conductivity are predicted to vary with z{sup -1}, z{sup -2}, and z{sup -3}, respectively. In monodisperse granular media, the characteristic grain size ({lambda}) controls film hydraulics through {lambda}{sup -1} scaling of (1) the perimeter length per unit cross sectional area over which films occur, (2) the critical matric potential ({Psi}{sub c}) below which films control flow, and (3) the magnitude of the unsaturated hydraulic conductivity when {Psi} < {Psi}{sub c}. While it is recognized that finer textured sediments have higher unsaturated hydraulic conductivities than coarser sands at intermediate {Psi}, the {lambda}{sup -1} scaling of hydraulic conductivity predicted here extends this understanding to very low saturations where all pores are drained. Extremely low unsaturated hydraulic conductivities are predicted under adsorbed film-controlled conditions (generally < 0.1 mm y{sup -1}). On flat surfaces, the film hydraulic diffusivity is shown to be constant (invariant with respect to {Psi}).

  20. Density functional studies of small Au clusters adsorbed on α-FeOOH: Structural and electronic properties

    NASA Astrophysics Data System (ADS)

    Fortunato, Leandro F.; Zubieta, Carolina E.; Fuente, Silvia A.; Belelli, Patricia G.; Ferullo, Ricardo M.

    2016-11-01

    We report a density functional theory (DFT) investigation on the interaction of tiny Aun (n = 1-5) clusters with the bare and hydroxylated (110) surfaces of goethite (α-FeOOH). Both adsorption and atom-by-atom nucleation processes were modeled. The adsorption is shown to be strong on the bare surface and takes place preferentially through the interaction of Au atoms with unsaturated surface oxygen anions, accompanied with an electronic charge transfer from the metal to the support. Au3, Au4 and Au5 planar structures resulted to be particularly stable due to polarization effects; indeed, Coulombic repulsion between basal Au atoms and surface oxygen anions promotes the displacement of the electronic density toward terminal Au atoms producing a Au+δ(basal)/Au-δ(terminal) polarization. On the hydroxylated surface, Au clusters adsorb more weakly with respect to the bare surface, mainly through monocoordinated surface hydroxyl groups and tricoordinated oxygen ions. Concerning the nucleation mechanism, while on the hydroxylated surface the nucleation energy is governed by the spin of the interacting systems, on the bare surface polarization effects seems to play a predominant role.

  1. Competition between Displacement and Dissociation of a Strong Acid Compared to a Weak Acid Adsorbed on Silica Particle Surfaces: The Role of Adsorbed Water.

    PubMed

    Fang, Yuan; Tang, Mingjin; Grassian, Vicki H

    2016-06-16

    The adsorption of nitric (HNO3) and formic (HCOOH) acids on silica particle surfaces and the effect of adsorbed water have been investigated at 296 K using transmission FTIR spectroscopy. Under dry conditions, both nitric and formic acids adsorb reversibly on silica. Additionally, the FTIR spectra show that both of these molecules remain in the protonated form. At elevated relative humidities (RH), adsorbed water competes both for surface adsorption sites with these acids as well as promotes their dissociation to hydronium ions and the corresponding anions. Compared to HNO3, the extent of dissociation is much smaller for HCOOH, very likely because it is a weaker acid. This study provides valuable insights into the interaction of HNO3 and HCOOH with silica surface on the molecular level and further reveals the complex roles of surface-adsorbed water in atmospheric heterogeneous chemistry of mineral dust particles-many of these containing silica.

  2. Competition between Displacement and Dissociation of a Strong Acid Compared to a Weak Acid Adsorbed on Silica Particle Surfaces: The Role of Adsorbed Water.

    PubMed

    Fang, Yuan; Tang, Mingjin; Grassian, Vicki H

    2016-06-16

    The adsorption of nitric (HNO3) and formic (HCOOH) acids on silica particle surfaces and the effect of adsorbed water have been investigated at 296 K using transmission FTIR spectroscopy. Under dry conditions, both nitric and formic acids adsorb reversibly on silica. Additionally, the FTIR spectra show that both of these molecules remain in the protonated form. At elevated relative humidities (RH), adsorbed water competes both for surface adsorption sites with these acids as well as promotes their dissociation to hydronium ions and the corresponding anions. Compared to HNO3, the extent of dissociation is much smaller for HCOOH, very likely because it is a weaker acid. This study provides valuable insights into the interaction of HNO3 and HCOOH with silica surface on the molecular level and further reveals the complex roles of surface-adsorbed water in atmospheric heterogeneous chemistry of mineral dust particles-many of these containing silica. PMID:27220375

  3. An innovative zinc oxide-coated zeolite adsorbent for removal of humic acid.

    PubMed

    Wang, Lingling; Han, Changseok; Nadagouda, Mallikarjuna N; Dionysiou, Dionysios D

    2016-08-01

    Zinc oxide (ZnO)-coated zeolite adsorbents were developed by both nitric acid modification and Zn(NO3)2·6H2O functionalization of zeolite 4A. The developed adsorbents were used for the removal of humic acid (HA) from aqueous solutions. The synthesized materials were characterized by porosimetry analysis, scanning electron microscopy, X-Ray diffraction analysis, and high resolution transmission electron microscopy. The maximum adsorption capacity of the adsorbents at 21±1°C was about 60mgCg(-1). The results showed that the positive charge density of ZnO-coated zeolite adsorbents was proportional to the amount of ZnO coated on zeolite and thus, ZnO-coated zeolite adsorbents exhibited a greater affinity for negatively charged ions. Furthermore, the adsorption capacity of ZnO-coated zeolite adsorbents increased markedly after acid modification. Adsorption experiments demonstrated ZnO-coated zeolite adsorbents possessed high adsorption capacity to remove HA from aqueous solutions mainly due to strong electrostatic interactions between negative functional groups of HA and the positive charges of ZnO-coated zeolite adsorbents.

  4. Adsorbate modification of the structural, electronic, and magnetic properties of ferromagnetic fcc {110} surfaces

    NASA Astrophysics Data System (ADS)

    Gunn, D. S. D.; Jenkins, Stephen J.

    2011-03-01

    We identify trends in structural, electronic, and magnetic modifications that occur on ferromagnetic {110} surfaces upon varying either the substrate material or the adsorbate species. First, we have modeled the adsorption of several first-row p-block elements on the surface of fcc Co{110} at two coverages [0.5 and 1.0 monolayer (ML)]. All adsorbates were found to expand the distance between the first and second substrate layers and to contract the distance between the second and third layers. The energetic location of a characteristic trough in the density-of-d-states difference plot correlates with the direction of the adsorbate magnetic coupling to the surface, and a trend of antiferromagnetic to ferromagnetic coupling to the surface was observed across the elements from boron to fluorine. A high fluorine adatom coverage (1.0 ML) was found to enhance the surface spin magnetic moment by 11%. Second, we also calculate and contrast adsorption of 0.5 and 1.0 ML of carbon, nitrogen, and oxygen adatoms on fcc iron, cobalt, and nickel {110} surfaces and compare the structural, electronic, and magnetic properties of these systems. Carbon and nitrogen are found to couple antiferromagnetically, and oxygen ferromagnetically, to all surfaces. It was found that antiferromagnetically coupled adsorbates retained their largest spin moment values on iron, whereas ferromagnetically coupled adsorbates possessed their lowest moments on this surface. The strongly localized influence of these adsorbates is clearly illustrated in partial density-of-states plots for the surface atoms.

  5. Oxygen Therapy

    MedlinePlus

    Oxygen therapy is a treatment that provides you with extra oxygen. Oxygen is a gas that your body needs to function. Normally, your lungs absorb ... in your home. A different kind of oxygen therapy is called hyperbaric oxygen therapy. It uses oxygen ...

  6. K -shell ionization cross sections of Al, Si, S, Ca, and Zn for oxygen ions in the energy range 1. 1--8 MeV

    SciTech Connect

    Geretschlaeger, M. ); Smit, Z. ); Steinbauer, E. )

    1992-03-01

    {ital K}-shell ionization cross sections induced by 1.1--8-MeV oxygen ions in Al, Si, S, Ca, and Zn were measured using different target thicknesses. The cross sections for vanishingly thin and for charge-equilibrium targets were obtained by extrapolation. The experimental results are compared to the perturbed stationary-state approximation with energy-loss, Coulomb, and relativistic corrections (ECPSSR) cross sections (Brandt and Lapicki, Phys. Rev. A 23, 1717 (1981)), to the modification of the ECPSSR theory (MECPSSR) (Benka, Geretschlaeger, and Paul, J. Phys. (Paris) Colloq. Suppl. 12, C9-251 (1987)), to the theory for direct Coulomb ionization of the 1{ital s}{sigma} molecular orbital (Montenegro and Sigaud, J. Phys. B 18, 299 (1985)), and to several semiclassical approximation codes using either the united atom binding procedure or the variational approach of Andersen {ital et} {ital al}. (Nucl. Instrum. Methods 192, 79 (1982)). The cross sections were also compared to the statistical molecular-orbital theory of inner-shell ionization for (nearly) symmetric atomic collisions (Mittelman and Wilets, Phys. Rev. 154, 12 (1967)). For fast collisions ({xi}{similar to}1), the ionization cross sections are well reproduced by theories for direct Coulomb ionization. For slower collisions ({xi}{lt}1), the experimental cross sections are systematically higher than the direct-ionization values, but they agree satisfactorily with the summed cross sections for direct Coulomb ionization and for molecular-orbital ionization. Best agreement (within a factor of 2) was found for the sums of MECPSSR and statistical cross sections.

  7. p-type conduction from Sb-doped ZnO thin films grown by dual ion beam sputtering in the absence of oxygen ambient

    SciTech Connect

    Kumar Pandey, Sushil; Kumar Pandey, Saurabh; Awasthi, Vishnu; Kumar, Ashish; Mukherjee, Shaibal; Deshpande, Uday P.; Gupta, Mukul

    2013-10-28

    Sb-doped ZnO (SZO) thin films were deposited on c-plane sapphire substrates by dual ion beam sputtering deposition system in the absence of oxygen ambient. The electrical, structural, morphological, and elemental properties of SZO thin films were studied for films grown at different substrate temperatures ranging from 200 °C to 600 °C and then annealed in situ at 800 °C under vacuum (pressure ∼5 × 10{sup −8} mbar). Films grown for temperature range of 200–500 °C showed p-type conduction with hole concentration of 1.374 × 10{sup 16} to 5.538 × 10{sup 16} cm{sup −3}, resistivity of 66.733–12.758 Ω cm, and carrier mobility of 4.964–8.846 cm{sup 2} V{sup −1} s{sup −1} at room temperature. However, the film grown at 600 °C showed n-type behavior. Additionally, current-voltage (I–V) characteristic of p-ZnO/n-Si heterojunction showed a diode-like behavior, and that further confirmed the p-type conduction in ZnO by Sb doping. X-ray diffraction measurements showed that all SZO films had (002) preferred crystal orientation. X-ray photoelectron spectroscopy analysis confirmed the formation of Sb{sub Zn}–2V{sub Zn} complex caused acceptor-like behavior in SZO films.

  8. Defect and adsorbate induced ferromagnetic spin-order in magnesium oxide nanocrystallites

    NASA Astrophysics Data System (ADS)

    Kumar, Ashok; Kumar, Jitendra; Priya, Shashank

    2012-05-01

    We report the correlation between d0 ferromagnetism, photoluminescence (PL), and adsorbed hydrogen (H-) species in magnesium oxide (MgO) nanocrystallites. Our study suggests that the oxygen vacancies, namely singly ionized anionic vacancies (F+) and dimers (F22+) induce characteristic photoluminescence and the room-temperature ferromagnetic spin-order. Nanocrystallites with low population of oxygen vacancies have revealed diamagnetic behavior. Intriguingly, on adsorption of hydrogen (H-) species in the MgO nanocrystallites, ferromagnetic behavior was either enhanced (in the case of highly oxygen deficient nanocrystallites) or begun to percolate (in the case of nanocrystallite with low population density of oxygen vacancies).

  9. A novel fiber-based adsorbent technology

    SciTech Connect

    Reynolds, T.A.

    1997-10-01

    In this Phase I Small Business Innovation Research program, Chemica Technologies, Inc. is developing an economical, robust, fiber-based adsorbent technology for removal of heavy metals from contaminated water. The key innovation is the development of regenerable adsorbent fibers and adsorbent fiber cloths that have high capacity and selectivity for heavy metals and are chemically robust. The process has the potential for widespread use at DOE facilities, mining operations, and the chemical process industry.

  10. Performance evaluation of low cost adsorbents in reduction of COD in sugar industrial effluent.

    PubMed

    Parande, Anand K; Sivashanmugam, A; Beulah, H; Palaniswamy, N

    2009-09-15

    Studies on reduction of chemical oxygen demand (COD) in effluent from sugar industry have been carried out by employing different absorbents optimizing various parameters, such as initial concentration of adsorbate, pH, adsorbent dosage and contact time. Experimental studies were carried out in batches using metakaolin, tamarind nut carbon and dates nut carbon as adsorbents by keeping initial adsorbent dosage at 1 g l(-1), agitation time over a range of 30-240 min, adsorbent dosage at 100-800 mg l(-1) by varying the pH range from 4 to 10. Characterization of there adsorbents were done using techniques such as Fourier transforms infra red spectroscopy (FTIR), X-ray diffraction (XRD) and scanning electron microscope (SEM). The experimental adsorption data fitted well to Langmuir and Freundlich adsorption isotherms. The isotherms of the adsorbents indicate appreciable adsorption capacity. Higher COD removal was observed at neutral pH conditions. Studies reveal that maximum reduction efficiency of COD takes place using metakaolin as an absorbent at a dosage of 500 mg l(-1) in a contact time of 180 min at pH 7 and it could be used as an efficient absorbent for treating sugar industrial effluent.

  11. Adsorption of oxygen and 1-butene on magnesium ferrite

    SciTech Connect

    Samuilova, O.K.; Kozlova, M.M.; Yagodovskii, V.D.

    1986-08-01

    The kinetics of the adsorption of oxygen and 1-butene on magnesium ferrite was studied. Conductometry and thermal desorption methods were used to investigate the adsorption of oxygen on magnesium ferrite. Two forms of adsorbed oxygen were found. The formation of these forms affects the kinetics of the adsorption of 1-butene.

  12. Quasiparticle excitations of adsorbates on doped graphene

    NASA Astrophysics Data System (ADS)

    Lischner, Johannes; Wickenburg, Sebastian; Wong, Dillon; Karrasch, Christoph; Wang, Yang; Lu, Jiong; Omrani, Arash A.; Brar, Victor; Tsai, Hsin-Zon; Wu, Qiong; Corsetti, Fabiano; Mostofi, Arash; Kawakami, Roland K.; Moore, Joel; Zettl, Alex; Louie, Steven G.; Crommie, Mike

    Adsorbed atoms and molecules can modify the electronic structure of graphene, but in turn it is also possible to control the properties of adsorbates via the graphene substrate. In my talk, I will discuss the electronic structure of F4-TCNQ molecules on doped graphene and present a first-principles based theory of quasiparticle excitations that captures the interplay of doping-dependent image charge interactions between substrate and adsorbate and electron-electron interaction effects on the molecule. The resulting doping-dependent quasiparticle energies will be compared to experimental scanning tunnelling spectra. Finally, I will also discuss the effects of charged adsorbates on the electronic structure of doped graphene.

  13. Development Trends in Porous Adsorbents for Carbon Capture.

    PubMed

    Sreenivasulu, Bolisetty; Sreedhar, Inkollu; Suresh, Pathi; Raghavan, Kondapuram Vijaya

    2015-11-01

    Accumulation of greenhouse gases especially CO2 in the atmosphere leading to global warming with undesirable climate changes has been a serious global concern. Major power generation in the world is from coal based power plants. Carbon capture through pre- and post- combustion technologies with various technical options like adsorption, absorption, membrane separations, and chemical looping combustion with and without oxygen uncoupling have received considerable attention of researchers, environmentalists and the stake holders. Carbon capture from flue gases can be achieved with micro and meso porous adsorbents. This review covers carbonaceous (organic and metal organic frameworks) and noncarbonaceous (inorganic) porous adsorbents for CO2 adsorption at different process conditions and pore sizes. Focus is also given to noncarbonaceous micro and meso porous adsorbents in chemical looping combustion involving insitu CO2 capture at high temperature (>400 °C). Adsorption mechanisms, material characteristics, and synthesis methods are discussed. Attention is given to isosteric heats and characterization techniques. The options to enhance the techno-economic viability of carbon capture techniques by integrating with CO2 utilization to produce industrially important chemicals like ammonia and urea are analyzed. From the reader's perspective, for different classes of materials, each section has been summarized in the form of tables or figures to get a quick glance of the developments.

  14. Phosphate adsorption on aluminum-impregnated mesoporous silicates: surface structure and behavior of adsorbents.

    PubMed

    Shin, Eun Woo; Han, James S; Jang, Min; Min, Soo-Hong; Park, Jae Kwang; Rowell, Roger M

    2004-02-01

    Phosphorus from excess fertilizers and detergents ends up washing into lakes, creeks, and rivers. This overabundance of phosphorus causes excessive aquatic plant and algae growth and depletes the dissolved oxygen supply in the water. In this study, aluminum-impregnated mesoporous adsorbents were tested for their ability to remove phosphate from water. The surface structure of the materials was investigated with X-ray diffraction (XRD), a N2 adsorption-desorption technique, Fourier transform-infrared (FT-IR), and X-ray photoelectron spectroscopy (XPS) to understand the effect of surface properties on the adsorption behavior of phosphate. The mesoporous materials were loaded with Al components by reaction with surface silanol groups. In the adsorption test, the Al-impregnated mesoporous materials showed fast adsorption kinetics as well as high adsorption capacities, compared with activated alumina. The uniform mesopores of the Al-impregnated mesoporous materials caused the diffusion rate in the adsorption process to increase, which in turn caused the fast adsorption kinetics. High phosphate adsorption capacities of the Al-impregnated mesoporous materials were attributed to not only the increase of surface hydroxyl density on Al oxide due to well-dispersed impregnation of Al components but also the decrease in stoichiometry of surface hydroxyl ions to phosphate by the formation of monodentate surface complexes. PMID:14968882

  15. Coordination structure of adsorbed Zn(II) at Water-TiO2 interfaces

    SciTech Connect

    He, G.; Pan, G.; Zhang, M.; Waychunas, G.A.

    2011-01-15

    The local structure of aqueous metal ions on solid surfaces is central to understanding many chemical and biological processes in soil and aquatic environments. Here, the local coordination structure of hydrated Zn(II) at water-TiO{sub 2} interfaces was identified by extended X-ray absorption fine structure (EXAFS) and X-ray absorption near-edge structure (XANES) spectroscopy combined with density functional theory (DFT) calculations. A nonintegral coordination number of average {approx}4.5 O atoms around a central Zn atom was obtained by EXAFS analysis. DFT calculations indicated that this coordination structure was consistent with the mixture of 4-coordinated bidentate binuclear (BB) and 5-coordinated bidentate mononuclear (BM) metastable equilibrium adsorption (MEA) states. The BB complex has 4-coordinated Zn, while the monodentate mononuclear (MM) complex has 6-coordinated Zn, and a 5-coordinated adsorbed Zn was found in the BM adsorption mode. DFT calculated energies showed that the lower-coordinated BB and BM modes were thermodynamically more favorable than the higher-coordinated MM MEA state. The experimentally observed XANES fingerprinting provided additional direct spectral evidence of 4- and 5-coordinated Zn-O modes. The overall spectral and computational evidence indicated that Zn(II) can occur in 4-, 5-, and 6-oxygen coordinated sites in different MEA states due to steric hindrance effects, and the coexistence of different MEA states formed the multiple coordination environments.

  16. Structural features of polymer adsorbent LiChrolut EN and interfacial behavior of water and water/organic mixtures.

    PubMed

    Gun'ko, V M; Turov, V V; Zarko, V I; Nychiporuk, Y M; Goncharuk, E V; Pakhlov, E M; Yurchenko, G R; Kulik, T V; Palyanytsya, B B; Borodavka, T V; Krupskaya, T V; Leboda, R; Skubiszewska-Zieba, J; Osovskii, V D; Ptushinskii, Y G; Turov, A V

    2008-07-01

    The structural and adsorption characteristics of polymer adsorbent LiChrolut EN and the behavior of adsorbed water and water/organic mixtures were studied using adsorption, microcalorimetry, transmission and scanning electron microscopy, mass spectrometry, infrared spectroscopy, 1H NMR spectroscopy with layer-by-layer freezing-out of liquids (190-273 K), and thermally stimulated depolarization current method (90-265 K). This adsorbent is characterized by large specific surface area (approximately 1500 m2/g) and pore volume (0.83 cm3/g) with a major contribution of narrow pores (R<10 nm) of a complicated shape (long hysteresis loop is in nitrogen adsorption-desorption isotherm). The adsorbent includes aromatic and aliphatic structures and oxygen-containing functionalities and can effectively adsorb organics and water/organic mixtures. On co-adsorption of water and organics (dimethyl sulfoxide, chloroform, methane), there is a weak influence of one on another adsorbate due to their poor mixing in pores. Weakly polar chloroform displaces a fraction of water from narrow pores. These effects can explain high efficiency of the adsorbent in solid-phase extraction of organics from aqueous solutions. The influence of structural features of several carbon and polymer adsorbents on adsorbed nitrogen, water and water/organics is compared on the basis of the adsorption and 1H NMR data. PMID:18440015

  17. Prussian blue caged in spongiform adsorbents using diatomite and carbon nanotubes for elimination of cesium.

    PubMed

    Hu, Baiyang; Fugetsu, Bunshi; Yu, Hongwen; Abe, Yoshiteru

    2012-05-30

    We developed a spongiform adsorbent that contains Prussian blue, which showed a high capacity for eliminating cesium. An in situ synthesizing approach was used to synthesize Prussian blue inside diatomite cavities. Highly dispersed carbon nanotubes (CNTs) were used to form CNT networks that coated the diatomite to seal in the Prussian blue particles. These ternary (CNT/diatomite/Prussian-blue) composites were mixed with polyurethane (PU) prepolymers to produce a quaternary (PU/CNT/diatomite/Prussian-blue), spongiform adsorbent with an in situ foaming procedure. Prussian blue was permanently immobilized in the cell walls of the spongiform matrix and preferentially adsorbed cesium with a theoretical capacity of 167 mg/g cesium. Cesium was absorbed primarily by an ion-exchange mechanism, and the absorption was accomplished by self-uptake of radioactive water by the quaternary spongiform adsorbent.

  18. Complete braided adsorbent for marine testing to demonstrate 3g-U/kg-adsorbent

    SciTech Connect

    Janke, Chris; Yatsandra, Oyola; Mayes, Richard; none,; Gill, Gary; Li-Jung, Kuo; Wood, Jordana; Sadananda, Das

    2014-04-30

    ORNL has manufactured four braided adsorbents that successfully demonstrated uranium adsorption capacities ranging from 3.0-3.6 g-U/kg-adsorbent in marine testing at PNNL. Four new braided and leno woven fabric adsorbents have also been prepared by ORNL and are currently undergoing marine testing at PNNL.

  19. Dynamics of ion bombardment-induced modifications of Si(001) at the radio-frequency-biased electrode in low-pressure oxygen plasmas: In situ spectroscopic ellipsometry and Monte Carlo study

    SciTech Connect

    Amassian, A.; Svec, M.; Desjardins, P.; Martinu, L.

    2006-09-15

    Low-pressure O{sub 2} plasma exposures were performed on c-Si(001) at a radio frequency (rf)-powered electrode in the presence of substrate self-biasing (V{sub B}) from V{sub B}=-60 to -600 V, in order to evaluate ion-surface interactions at the growth surface under ion bombardment conditions suitable for the fabrication of high quality optical coatings. The plasma-surface interactions were monitored in situ using real-time spectroscopic ellipsometry (RTSE), which reveals time- and ion-fluence-resolved information about depth-dependent modifications, such as damage and oxidation below the c-Si substrate surface. RTSE analysis indicates almost immediate damage formation (<<1 s) to a depth of a few nanometers below the surface after exposure to a low oxygen ion fluence ({approx}5x10{sup 14} O cm{sup -2}). Oxide growth is detected at intermediate fluence ({approx}10{sup 15}-10{sup 16} O cm{sup -2}) and is attributed to O subplantation (shallow implantation); it forms near the surface of the target on top of an O-deficient interfacial damage layer (DL). Both layers experience a self-limiting growth behavior at high fluence (>10{sup 17} cm{sup -2}) as oxide and DL thicknesses reach bias-dependent steady-state values, determined by the maximum ion penetration depth, which increases from {approx}3.6 to 9.5 nm for V{sub B}=-60 to -600 V. The in situ experimental study was complemented by Monte Carlo TRIDYN simulations based on the binary collision approximation, which were modified to calculate dynamic changes in the composition of a target exposed to a broad-energy ion source (rf plasma source) at high fluence. Simulation results are found to agree exceptionally well with experiment. In addition, they reveal that the 1.2-3.5-nm-thick DL formed in the steady-state regime is a result of (1) damage formation due to the presence of a small number of high energy O{sup +} ions in the plasma environment, capable of penetrating and damaging up to 3 nm deeper than the majority ion

  20. Database of Novel and Emerging Adsorbent Materials

    National Institute of Standards and Technology Data Gateway

    SRD 205 NIST/ARPA-E Database of Novel and Emerging Adsorbent Materials (Web, free access)   The NIST/ARPA-E Database of Novel and Emerging Adsorbent Materials is a free, web-based catalog of adsorbent materials and measured adsorption properties of numerous materials obtained from article entries from the scientific literature. Search fields for the database include adsorbent material, adsorbate gas, experimental conditions (pressure, temperature), and bibliographic information (author, title, journal), and results from queries are provided as a list of articles matching the search parameters. The database also contains adsorption isotherms digitized from the cataloged articles, which can be compared visually online in the web application or exported for offline analysis.