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Sample records for doped lanthanum chromites

  1. Cobalt doped lanthanum chromite material suitable for high temperature use

    DOEpatents

    Ruka, R.J.

    1986-12-23

    A high temperature, solid electrolyte electrochemical cell, subject to thermal cycling temperatures of between about 25 C and about 1,200 C, capable of electronic interconnection to at least one other electrochemical cell and capable of operating in an environment containing oxygen and a fuel, is made; where the cell has a first and second electrode with solid electrolyte between them, where an improved interconnect material is applied along a portion of a supporting electrode; where the interconnect is made of a chemically modified lanthanum chromite, containing cobalt as the important additive, which interconnect allows for adjustment of the thermal expansion of the interconnect material to more nearly match that of other cell components, such as zirconia electrolyte, and is stable in oxygen containing atmospheres such as air and in fuel environments. 2 figs.

  2. Cobalt doped lanthanum chromite material suitable for high temperature use

    DOEpatents

    Ruka, Roswell J.

    1986-01-01

    A high temperature, solid electrolyte electrochemical cell, subject to thermal cycling temperatures of between about 25.degree. C. and about 1200.degree. C., capable of electronic interconnection to at least one other electrochemical cell and capable of operating in an environment containing oxygen and a fuel, is made; where the cell has a first and second electrode with solid electrolyte between them, where an improved interconnect material is applied along a portion of a supporting electrode; where the interconnect is made of a chemically modified lanthanum chromite, containing cobalt as the important additive, which interconnect allows for adjustment of the thermal expansion of the interconnect material to more nearly match that of other cell components, such as zirconia electrolyte, and is stable in oxygen containing atmospheres such as air and in fuel environments.

  3. Method and closing pores in a thermally sprayed doped lanthanum chromite interconnection layer

    DOEpatents

    Singh, Prabhakar; Ruka, Roswell J.

    1995-01-01

    A dense, substantially gas-tight electrically conductive interconnection layer is formed on an air electrode structure of an electrochemical cell by (A) providing an air electrode surface; (B) forming on a selected portion of the electrode surface, a layer of doped LaCrO.sub.3 particles doped with an element or elements selected from Ca, Sr, Ba, Mg, Co, Ni, Al and mixtures thereof by thermal spraying doped LaCrO.sub.3 particles, either by plasma arc spraying or flame spraying; (C) depositing a mixture of CaO and Cr.sub.2 O.sub.3 on the surface of the thermally sprayed layer; and (D) heating the doped LaCrO.sub.3 layer coated with CaO and Cr.sub.2 O.sub.3 surface deposit at from about 1000.degree. C. to 1200.degree. C. to substantially close the pores, at least at a surface, of the thermally sprayed doped LaCrO.sub.3 layer. The result is a dense, substantially gas-tight, highly doped, electrically conductive interconnection material bonded to the electrode surface. A solid electrolyte layer can be applied to the nonselected portion of the air electrode. A fuel electrode can be applied to the solid electrolyte, to form an electrochemical cell, for example for generation of electrical power.

  4. Method and closing pores in a thermally sprayed doped lanthanum chromite interconnection layer

    DOEpatents

    Singh, P.; Ruka, R.J.

    1995-02-14

    A dense, substantially gas-tight electrically conductive interconnection layer is formed on an air electrode structure of an electrochemical cell by (A) providing an air electrode surface; (B) forming on a selected portion of the electrode surface, a layer of doped LaCrO{sub 3} particles doped with an element or elements selected from Ca, Sr, Ba, Mg, Co, Ni, Al and mixtures thereof by thermal spraying doped LaCrO{sub 3} particles, either by plasma arc spraying or flame spraying; (C) depositing a mixture of CaO and Cr{sub 2}O{sub 3} on the surface of the thermally sprayed layer; and (D) heating the doped LaCrO{sub 3} layer coated with CaO and Cr{sub 2}O{sub 3} surface deposit at from about 1,000 C to 1,200 C to substantially close the pores, at least at a surface, of the thermally sprayed doped LaCrO{sub 3} layer. The result is a dense, substantially gas-tight, highly doped, electrically conductive interconnection material bonded to the electrode surface. A solid electrolyte layer can be applied to the nonselected portion of the air electrode. A fuel electrode can be applied to the solid electrolyte, to form an electrochemical cell, for example for generation of electrical power. 5 figs.

  5. Mechanical properties of lanthanum and yttrium chromites

    SciTech Connect

    Paulik, S.W.; Armstrong, T.R.

    1996-12-31

    In an operating high-temperature (1000{degrees}C) solid oxide fuel cell (SOFC), the interconnect separates the fuel (P(O{sub 2}){approx}10{sup -16} atm) and the oxidant (P(O2){approx}10{sup 0.2} atm), while being electrically conductive and connecting the cells in series. Such severe atmospheric and thermal demands greatly reduce the number of viable candidate materials. Only two materials, acceptor substituted lanthanum chromite and yttrium chromite, meet these severe requirements. In acceptor substituted chromites (Sr{sup 2+} or Ca{sup 2+} for La{sup 3+}), charge compensation is primarily electronic in oxidizing conditions (through the formation of Cr{sup 4+}). Under reducing conditions, ionic charge compensation becomes significant as the lattice becomes oxygen deficient. The formation of oxygen vacancies is accompanied by the reduction of Cr{sup 4+} ions to Cr{sup 3+} and a resultant lattice expansion. The lattice expansion observed in large chemical potential gradients is not desirable and has been found to result in greatly reduced mechanical strength.

  6. Tape method of forming a thin layer of doped lanthanum chromite particles and of bonding such on an electrode

    DOEpatents

    Richards, Von L.; Singhal, Subhash C.; Pal, Uday B.

    1992-01-01

    A combustible polymer film, useful for application of an interconnection on an electrode is made by: (1) providing doped LaCro.sub.3 particles; (2) dispersing doped LaCrO.sub.3 particles in a solvent, to provide a dispersion; (3) screening the dispersion to provide particles in the range of from 30 micrometers to 80 micrometers; (4) admixing a fugitive polymer with the particles; (5) casting the dispersion to provide a film; (6) drying the film; and (7) stripping the film. The film can then be applied to a porous, preheated electrode top surface, and then electrochemical vapor depositing a dense skeletal LaCrO.sub.3 structure, between and around the doped LaCrO.sub.3 particles. Additional solid oxide electrolyte and fuel electrode layers can then be added to provide a fuel cell.

  7. Tape method of forming a thin layer of doped lanthanum chromite particles and of bonding such on an electrode

    DOEpatents

    Richards, V.L.; Singhal, S.C.; Pal, U.B.

    1992-07-21

    A combustible polymer film, useful for application of an interconnection on an electrode is made by: (1) providing doped LaCro[sub 3] particles; (2) dispersing doped LaCrO[sub 3] particles in a solvent, to provide a dispersion; (3) screening the dispersion to provide particles in the range of from 30 micrometers to 80 micrometers; (4) admixing a fugitive polymer with the particles; (5) casting the dispersion to provide a film; (6) drying the film; and (7) stripping the film. The film can then be applied to a porous, preheated electrode top surface, and then a dense skeletal LaCrO[sub 3] structure is electrochemically vapor deposited between and around the doped LaCrO[sub 3] particles. Additional solid oxide electrolyte and fuel electrode layers can then be added to provide a fuel cell. 4 figs.

  8. Infiltrated lanthanum strontium chromite anodes for solid oxide fuel cells: Structural and catalytic aspects

    NASA Astrophysics Data System (ADS)

    Oh, Tae-Sik; Yu, Anthony S.; Adijanto, Lawrence; Gorte, Raymond J.; Vohs, John M.

    2014-09-01

    Infiltration is a widely used fabrication method for solid oxide fuel cell (SOFC) composite electrodes. Here we report a study of the structure and electrocatalytic properties of SOFC anodes composed of a layer of lanthanum, strontium chromite (La0.8Sr0.2CrO3, LSCr), both with and without added transition metal dopants, infiltrated into a porous yttria-stabilized zirconia (YSZ) matrix. The structural evolution of the electrode upon reduction and under typical SOFC operating conditions is compared to that reported previously for La0.8Sr0.2Cr0.5Mn0.5O3-YSZ composite anodes. For the transition metal doped materials, a portion of the metal dopants were found to be exsolved from the LSCr lattice upon reduction and to be effective in promoting electro-oxidation of hydrogen. Exsolved cobalt particles were also found to be relatively stable when exposed to hydrocarbon fuels with low activity for the formation of carbon deposits.

  9. Preparation and Charge Density in (Co, Fe)-Doped La-Ca-Based Chromite

    NASA Astrophysics Data System (ADS)

    Saravanan, R.; Thenmozhi, N.; Fu, Yen-Pei

    2016-08-01

    Transition metal-doped lanthanum chromites (La0.8Ca0.2)(Cr0.9- x Co0.1Fe x )O3 ( x = 0.03, 0.06, 0.09, 0.12) have been synthesized by solid state reaction method. The synthesized samples were characterized for their structural properties using powder x-ray diffraction analysis, which shows that the grown samples are orthorhombic in structure with single phase. The nature of bonding and the charge distribution of the grown samples have been analyzed by maximum entropy method. Further, the samples were characterized for their optical and magnetic properties using ultraviolet-visible spectra and vibrating sample magnetometry. The microstructural studies were carried by scanning electron microscopy/electron dispersive x-ray spectroscopy techniques. From the optical absorption spectra, it was found that the energy band gap of the samples ranges from 2.135 eV to 2.405 eV. From vibrating sample magnetometer measurements, ferromagnetic like behaviour with large coercive field was observed for Fe doping concentration of x = 0.12. Since the doped lanthanum chromites have good mechanical properties and electrical conductivity at high temperature, these materials are used in solid oxide fuel cells.

  10. Method of making highly sinterable lanthanum chromite powder

    DOEpatents

    Richards, Von L.; Singhal, Subhash C.

    1992-01-01

    A highly sinterable powder consisting essentially of LaCrO.sub.3, containing from 5 weight % to 20 weight % of a chromite of dopant Ca, Sr, Co, Ba, or Mg and a coating of a chromate of dopant Ca, Sr, Co, Ba, or Mg; is made by (1) forming a solution of La, Cr, and dopant; (2) heating their solutions; (3) forming a combined solution having a desired ratio of La, Cr, and dopant and heating to reduce solvent; (4) forming a foamed mass under vacuum; (5) burning off organic components and forming a charred material; (6) grinding the charred material; (7) heating the char at from 590.degree. C. to 950 C. in inert gas containing up to 50,000 ppm O.sub.2 to provide high specific surface area particles; (8) adding that material to a mixture of a nitrate of Cr and dopant to form a slurry; (9) grinding the particles in the slurry; (10) freeze or spray drying the slurry to provide a coating of nitrates on the particles; and (11) heating the coated particles to convert the nitrate coating to a chromate coating and provide a highly sinterable material having a high specific surface area of over 7 m.sup.2 /g.

  11. Method of making highly sinterable lanthanum chromite powder

    DOEpatents

    Richards, V.L.; Singhal, S.C.

    1992-09-01

    A highly sinterable powder consisting essentially of LaCrO[sub 3], containing from 5 weight % to 20 weight % of a chromite of dopant Ca, Sr, Co, Ba, or Mg and a coating of a chromate of dopant Ca, Sr, Co, Ba, or Mg; is made by (1) forming a solution of La, Cr, and dopant; (2) heating their solutions; (3) forming a combined solution having a desired ratio of La, Cr, and dopant and heating to reduce solvent; (4) forming a foamed mass under vacuum; (5) burning off organic components and forming a charred material; (6) grinding the charred material; (7) heating the char at from 590 C to 950 C in inert gas containing up to 50,000 ppm O[sub 2] to provide high specific surface area particles; (8) adding that material to a mixture of a nitrate of Cr and dopant to form a slurry; (9) grinding the particles in the slurry; (10) freeze or spray drying the slurry to provide a coating of nitrates on the particles; and (11) heating the coated particles to convert the nitrate coating to a chromate coating and provide a highly sinterable material having a high specific surface area of over 7 m[sup 2]/g. 2 figs.

  12. Sprayed lanthanum doped zinc oxide thin films

    NASA Astrophysics Data System (ADS)

    Bouznit, Y.; Beggah, Y.; Ynineb, F.

    2012-01-01

    Lanthanum doped zinc oxide thin films were deposited on soda-lime glass substrates using a pneumatic spray pyrolysis technique. The films were prepared using different lanthanum concentrations at optimum deposition parameters. We studied the variations in structural, morphological and optical properties of the samples due to the change of doping concentration in precursor solutions. X-ray diffraction (XRD) patterns show that pure and La-doped ZnO thin films are highly textured along c-axis perpendicular to the surface of the substrate. Scanning electron micrographs show that surface morphology of ZnO films undergoes a significant change according to lanthanum doping. All films exhibit a transmittance higher than 80% in the visible region.

  13. High Performance Ceramic Interconnect Material for Solid Oxide Fuel Cells (SOFCs): Ca- and Transition Metal-doped Yttrium Chromite

    SciTech Connect

    Yoon, Kyung J.; Stevenson, Jeffry W.; Marina, Olga A.

    2011-10-15

    The effect of transition metal substitution on thermal and electrical properties of Ca-doped yttrium chromite was investigated in relation to use as a ceramic interconnect in high temperature solid oxide fuel cells (SOFCs). 10 at% Co, 4 at% Ni, and 1 at% Cu substitution on B-site of 20 at% Ca-doped yttrium chromite led to a close match of thermal expansion coefficient (TEC) with that of 8 mol% yttria-stabilized zirconia (YSZ), and a single phase Y0.8Ca0.2Cr0.85Co0.1Ni0.04Cu0.01O3 remained stable between 25 and 1100 degree C over a wide oxygen partial pressure range. Doping with Cu significantly facilitated densification of yttrium chromite. Ni dopant improved both electrical conductivity and dimensional stability in reducing environments, likely through diminishing the oxygen vacancy formation. Substitution with Co substantially enhanced electrical conductivity in oxidizing atmosphere, which was attributed to an increase in charge carrier density and hopping mobility. Electrical conductivity of Y0.8Ca0.2Cr0.85Co0.1Ni0.04Cu0.01O3 at 900 degree C is 57 S/cm in air and 11 S/cm in fuel (pO2=5×10^-17 atm) environments. Chemical compatibility of doped yttrium chromite with other cell components was verified at the processing temperatures. Based on the chemical and dimensional stability, sinterability, and thermal and electrical properties, Y0.8Ca0.2Cr0.85Co0.1Ni0.04Cu0.01O3 is suggested as a promising SOFC ceramic interconnect to potentially overcome technical limitations of conventional acceptor-doped lanthanum chromites.

  14. Synthesis and characterization of lanthanum doped zinc oxide nanoparticles

    NASA Astrophysics Data System (ADS)

    Kumar, Vinod; Sonia, Suman, Kumar, Sacheen; Kumar, Dinesh

    2016-05-01

    La doped ZnO (Zn1-xLaxO, x = 0, 3, 6 and 9) were prepared via chemical co-precipitation method using Zinc Acetate, Lanthanum Acetate and Sodium Hydroxide at 50°C. Hydrate nanoparticles were annealed in air at 300°C for 3 hours. The synthesized samples have been characterized by powder X-ray diffraction and UV-Visiblespectrophotometer. The XRD measurement revealsthat the prepared nanoparticles have different microstructure without changing a hexagonal wurtzite structure. The result shows the change in nanoparticles size with the increment of lanthanum concentration for lower concentration for x = 0 to 6 and decreases at x = 9.

  15. Photocatalytic hydrogen generation over lanthanum doped TiO2 under UV light irradiation.

    PubMed

    Liu, Y; Xie, L; Li, Y; Qu, J L; Zheng, J; Li, X G

    2009-02-01

    TiO2 nanoparticles doped with different amount of lanthanum were obtained by sol-gel approach and followed annealing at different temperature. The crystal size of TiO2 doped with lanthanum was smaller than that of pure TiO2. Photocatalytic activity of TiO2 doped with lanthanum for water splitting into H2 was investigated. The photocatalytic activity of TiO2 doped with lanthanum for water splitting into H2 is higher than that of pure TiO2. It was found that the optimal photocatalyst was TiO2 doped with 2 wt% lanthanum and calcined at 600 degrees C for 4 h which had hydrogen generation rate 700.6 micromol h(-1).

  16. Thermal conductivity analysis of lanthanum doped manganites

    SciTech Connect

    Mansuri, Irfan; Shaikh, M. W.; Khan, E.; Varshney, Dinesh

    2014-04-24

    The temperature-dependent thermal conductivity of the doped manganites La{sub 0.7}Ca{sub 0.3}MnO{sub 3} is theoretically analyzed within the framework of Kubo formulae. The Hamiltonian consists of phonon, electron and magnon thermal conductivity contribution term. In this process we took defects, carrier, grain boundary, scattering process term and then calculate phonon, electron and magnon thermal conductivity.

  17. Lanthanum

    MedlinePlus

    ... and the laboratory. Your doctor will order certain lab tests to check your body's response to lanthanum.Before having any x-rays of your abdominal area, tell your doctor and the x-ray technicians that you are taking lanthanum.Do not let ...

  18. Europium doped lanthanum zirconate nanoparticles with high concentration quenching

    SciTech Connect

    Alaparthi, Suresh B.; Lu, Long; Tian, Yue; Mao, Yuanbing

    2014-01-01

    Graphical abstract: - Highlights: • Eu:La{sub 2}Zr{sub 2}O{sub 7} nanoparticles were prepared facilely by a kinetically modified molten salt method. • High color purity and concentration quenching were achieved in these La{sub 2}Zr{sub 2}O{sub 7}:Eu nanoparticles. • Concentration quenching mechanism was discussed for Eu{sup 3+} in these Eu:La{sub 2}Zr{sub 2}O{sub 7} nanoparticles. - Abstract: A series of Eu{sup 3+} doped lanthanum zirconate (La{sub 2}Zr{sub 2}O{sub 7}) nanoparticles (NPs, 20 ± 5 nm in diameter) with cubic fluorite structure were facilely synthesized by a kinetically modified molten salt synthetic (MSS) process and characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM) and photoluminescence spectra (PL). Under the excitation of 405 nm, intense red emission with high color purity can be observed in the Eu{sup 3+} doped La{sub 2}Zr{sub 2}O{sub 7} NPs. Moreover, the as-prepared Eu:La{sub 2}Zr{sub 2}O{sub 7} NPs possess high concentration quenching, which is as high as ∼32.5 mol% of europium dopants in the La{sub 2}Zr{sub 2}O{sub 7} host. The corresponding concentration quenching mechanism was discussed as well. Our results confirm that the kinetically modified MSS process is a promising approach for preparing rare earth (RE) ions doped A{sub 2}B{sub 2}O{sub 7} nanoparticles with uniform RE doping and high concentration quenching.

  19. The evolution mechanism of the dislocation loops in irradiated lanthanum doped cerium oxide

    NASA Astrophysics Data System (ADS)

    Miao, Yinbin; Aidhy, Dilpuneet; Chen, Wei-Ying; Mo, Kun; Oaks, Aaron; Wolf, Dieter; Stubbins, James F.

    2014-02-01

    Cerium dioxide, a non-radioactive surrogate of uranium dioxide, is useful for simulating the radiation responses of uranium dioxide and mixed oxide fuel (MOX). Controlled additions of lanthanum can also be used to form various levels of lattice oxide or anion vacancies. In previous transmission electron microscopy (TEM) experimental studies, the growth rate of dislocation loops in irradiated lanthanum doped ceria was reported to vary with lanthanum concentration. This work reports findings of the evolution mechanisms of the dislocation loops in cerium oxide with and without lanthanum dopants based on a combination of molecular statics and molecular dynamics simulations. These dislocation loops are found to be b = 1 / 3 < 1 1 1 > interstitial type Frank loops. Calculations of the defect energy profiles of the dislocation loops with different structural configurations and radii reveal the basis for preference of nucleation as well as the driving force of growth. Frenkel pair evolution simulations and displacement cascade overlaps simulations were conducted for a variety of lanthanum doping conditions. The nucleation and growth processes of the Frank loop were found to be controlled by the mobility of cation interstitials, which is significantly influenced by the lanthanum doping concentration. Competition mechanisms coupled with the mobility of cation point defects were discovered, and can be used to explain the lanthanum effects observed in experiments.

  20. Calcium- and Cobalt-doped Yttrium Chromites as an Interconnect Material for Solid Oxide Fuel Cells

    SciTech Connect

    Yoon, Kyung J.; Cramer, Carolyn N.; Thomsen, Edwin C.; Coyle, Christopher A.; Coffey, Greg W.; Marina, Olga A.

    2010-04-23

    The structural, thermal and electrical characteristics of calcium- and cobalt-doped yttrium chromites were studied for a potential use as the interconnect material in high temperature solid oxide fuel cells (SOFCs) as well as other high temperature electrochemical and thermoelectric devices. The Y0.8Ca0.2Cr1-xCoxO3±δ (x=0, 0.1, 0.2, 0.3) compositions had single phase orthorhombic perovskite structures in the wide range of oxygen pressures. Sintering behavior was remarkably enhanced upon cobalt doping and densities 95% and 97% of theoretical density were obtained after sintering at 1300oC in air, when x was 0.2 and 0.3, respectively. The electrical conductivity in both oxidizing and reducing atmospheres was significantly improved with cobalt content, and values of 49 and 10 S/cm at 850oC and 55 and 14 S/cm at 950oC in air and forming gas, respectively, were reported for x=0.2. The conductivity increase was attributed to the charge carrier density increase upon cobalt substitution for chromium confirmed with Seebeck measurements. The thermal expansion coefficient (TEC) was increased with cobalt content and closely matched to that of an 8 mol% yttria-stabilized zirconia (YSZ) electrolyte for 0.1 ≤ x ≤ 0.2. The chemical compatibility between Y0.8Ca0.2Cr1-xCoxO3±δ and YSZ was evaluated firing the two at 1400oC and no reaction products were found if x value was kept lower than 0.2.

  1. Structural and Conductivity Studies on Lanthanum Doped LiNiPO4 Prepared by Polyol Method

    NASA Astrophysics Data System (ADS)

    Karthickprabhu, S.; Hirankumar, G.; Maheswaran, A.; Bella, R. S. Daries; Sanjeeviraja, C.

    2013-07-01

    Pure and Lanthanum doped LiNiPO4 (with different Molar concentrations) have been prepared by polyol method using 1,2 propanediol as a polyol medium. XRD analysis reveal that sample calcined at 650°C for 6 hrs shows good crystalline nature with orthorhombic structure and this result is consistent with TG/DTA result. It is found that the conductivity enhances upon doping of Lanthanum while backhoprate decreases compared with pure LiNiPO4. Dielectric studies have also been discussed.

  2. Improvement of Sintering, Thermal Behavior, and Electrical Properties of Calcium- and Transition Metal-Doped Yttrium Chromite

    SciTech Connect

    Yoon, Kyung J.; Cramer, Carolyn N.; Stevenson, Jeffry W.; Marina, Olga A.

    2010-06-21

    The A-site calcium doped yttrium chromite was additionally doped with various transition metals on the B-site to improve the sintering, thermal behavior and electrical properties of these ceramics for future use as an interconnect material in high temperature solid oxide fuel cells (SOFC). With 10 % addition of Co, Cu, Ni, Fe, and Mn, the single phase orthorhombic perovskite structure remained stable over a wide range of oxygen partial pressures, as confirmed by X-ray diffraction. The substitution of Cu for chromium remarkably improved the sinterability and allowed full densification in air by sintering at 1400 degrees C. The substitution of Co and Ni significantly improved the electrical conductivity of yttrium chromites in both oxidizing and reducing environments. This was explained by the increase of charge carrier density with nickel and cobalt doping, as confirmed by Seebeck measurements. With 10% of nickel dopant, the electrical conductivity of Y0.8Ca0.2CrO3±δ increased from 12 to 38 S/cm in air and from 2 to 15 S/cm in reducing atmosphere at 950 degrees C. Mn doping had a negative effect on the sintering and electrical conductivity.

  3. Nanocrystalline brookite with enhanced stability and photocatalytic activity: influence of lanthanum(III) doping.

    PubMed

    Perego, Céline; Wang, Yu-Heng; Durupthy, Olivier; Cassaignon, Sophie; Revel, Renaud; Jolivet, Jean-Pierre

    2012-02-01

    Metastable TiO(2) polymorphs are more promising materials than rutile for specific applications such as photocatalysis or catalysis support. This was clearly demonstrated for the anatase phase but still under consideration for brookite, which is difficult to obtain as pure phase. Moreover, the surface doping of anatase with lanthanum ions is known to both increase the thermal stability of the metastable phase and improve its photocatalytic activity. In this study, TiO(2) nanoparticles of almost only the brookite structure were prepared by a simple sol-gel procedure in aqueous solution. The nanoparticles were then doped with lanthanum(III) ions. The thermal stability of the nanoparticles was analyzed by X-ray diffraction and kinetic models were successfully applied to quantify phases evolutions. The presence of surface-sorbed lanthanum(III) ions increased the phase stability of at least 200 °C and this temperature shift was attributed to the selective phase stabilization of metastable TiO(2) polymorphs. Moreover, the combination of the surface doping ions and the thermal treatment induces the vanishing of the secondary anatase phase, and the photocatalytic tests on the doped brookite nanoparticles demonstrated that the doping increased photocatalytic activity and that the extent depended on the duration of the sintering treatment.

  4. Effect of Lanthanum Doping on the Microstructure of Tin-Silver Solder Alloys

    NASA Astrophysics Data System (ADS)

    Pei, Min; Qu, Jianmin

    2008-03-01

    In this study, quantitative microstructure studies were performed on multiple length scales to investigate the effect of lanthanum (La) doping on Sn-Ag lead-free solder materials. Factors considered in this paper include doping amount, aging temperature, and aging time. It was found that La doping reduces the grain size significantly, and the reduced grain size remains stable during thermal aging. The size of the Ag3Sn particles is also greatly reduced by La doping, and the particles coarsen during thermal aging, albeit at a much reduced rate than in the undoped alloy. The rate of particle coarsening can be described by a cubic-root law. Another observation is that the interparticle spacing remains unaffected by the doping. Therefore, higher La doping level leads to higher volume fraction of the eutectic region due to the increased total number of Ag3Sn particles.

  5. Effect of Nickel Substitution on Defect Chemistry, Electrical Properties, and Dimensional Stability of Calcium-Doped Yttrium Chromite

    SciTech Connect

    Yoon, Kyung J.; Stevenson, Jeffry W.; Marina, Olga A.

    2011-06-30

    The effect of nickel substitution on defect chemistry, electrical properties, and dimensional stability of calcium-doped yttrium chromite was studied for use as an interconnect material in high temperature solid oxide fuel cells (SOFCs). The compositions of Y0.8Ca0.2Cr1-xNixO3±δ (x=0-0.15), prepared using the glycine nitrate process, showed single phase orthorhombic perovskite structures over a wide range of oxygen partial pressures (10^-17 atm ≤ pO2 ≤ 0.21 atm). X-ray diffraction (XRD) analysis indicated that most of the nickel ions replacing chromium ions are divalent and act as acceptor dopants, leading to a substantial increase in conductivity. In particular, the conductivity at 900 degree C in air increased from 10 S/cm to 34 S/cm with 15% nickel substitution, and an increase in charge carrier density was confirmed by Seebeck measurements. A point defect model was derived, and the relationship between electrical conductivity and oxygen partial pressure was successfully fitted into the proposed model. The defect modeling results indicated that nickel substitution improves the stability of calcium-doped yttrium chromite toward reduction and suppresses the oxygen vacancy formation, which results in significantly increased electrical conductivity in reducing environment. The electrical conductivity of Y0.8Ca0.2Cr0.85Ni0.15O3±δ at 900 degree C in reducing atmosphere (pO2=10^-17 atm) was 5.8 S/cm, which was more than an order of magnitude higher than that of Y0.8Ca0.2CrO3±δ (0.2 S/cm). Improved stability in reducing atmosphere was further confirmed by dilatometry measurements showing reduced isothermal "chemical" expansion, and the isothermal expansion in reducing atmosphere (pO2=10^-17 atm) at 900 degree C decreased from 0.07% for Y0.8Ca0.2CrO3±δ to 0.03% for Y0.8Ca0.2Cr0.85Ni0.15O3±δ. Based on these results, enhanced electrical performance and mechanical integrity is expected with nickel substitution on calcium-doped yttrium chromite in SOFC

  6. Deposition barium titanate (BaTiO3) doped lanthanum with chemical solution deposition

    NASA Astrophysics Data System (ADS)

    Iriani, Y.; Jamaludin, A.; Nurhadi, N.

    2016-11-01

    Deposition of Barium Titanate (BaTiO3) thin films used Chemical Solution Deposition (CSD) method and prepared with spin coater. BaTiO3 is doped with lanthanum, 1%, 2%, and 3%. The thermal process use annealing temperature 900°C and holding time for 3 hours. The result of characterization with x-ray diffraction (XRD) equipment show that the addition of La3+ doped on Barium Titanate caused the change of angle diffraction.The result of refine with GSAS software shows that lanthanum have been included in the structure of BaTiO3. Increasing mol dopant La3+ cause lattice parameter and crystal volume become smaller. Characterization result using Scanning Electron Microscopy (SEM) equipment show that grain size (grain size) become smaller with increasing mole dopant (x) La3+. The result of characterization using Sawyer Tower methods show that all the samples (Barium Titanante and Barium Titanate doped lanthanum) are ferroelectric material. Increasing of mole dopant La3+ cause smaller coercive field and remanent polarization increases.

  7. Luminescence properties of Dy3+ doped lanthanum-calcium-silicaborate glass scintillator

    NASA Astrophysics Data System (ADS)

    Park, J. M.; Ha, D. H.; Lee, S. W.; Chanthima, N.; Ruangtaweep, Y.; Kaewkhao, J.

    2016-09-01

    In this research Dy3+-doped lanthanum-calcium-silicaborate glass scintillators, with the formula 25La2O3: 10CaO: 10SiO2: (55-x)B2O3: xDy2O3, were fabricated by using the melt-quenching technique. For the Dy3+ doping concentrations from 0.05 mol% to 0.5 mol% studied the luminescence properties of the Dy3+-doped glass scintillators with various radiation sources, such as X-ray, photo-, laser, and proton. To understand the absorption state, we measured the transmittance spectrum. Furthermore, X-ray, photo- and proton-induced emission spectra were measured to study the transition states of Dy3+-doped glass scintillators. The laser-induced emission spectra were measured at low temperatures in the range from 10 K to 300 K.

  8. Effect of a-site cation deficiency and YSZ additions on sintering and properties of doped lanthanum manganite

    SciTech Connect

    Stevenson, J.W.; Armstrong, T.R.; Weber, W.J.

    1995-06-01

    The sintering behavior of Ca- and Sr-doped lanthanum manganite (the preferred SOFC cathode material) is highly dependent on the relative proportion of A and B site cations in the material. In general, A-site cation deficiency increases sintered density. The effect of additions of YSZ to lanthanum manganite (to expand the reactive region at the cathode/electrolyte interface and improve thermal expansion and sintering shrinkage matches) on sintering and other properties will also be reported.

  9. Heterogeneous photocatalytic decomposition of benzene on lanthanum-doped TiO2 film at ambient temperature.

    PubMed

    Zhang, Shicheng; Zheng, Zhijian; Wang, Jinhe; Chen, Jianmin

    2006-12-01

    Lanthanum-doped anatase TiO2 thin films on glass prepared via a sol-gel process have been shown to have much higher photocatalytic activity for the degradation of gaseous benzene than pure anatase TiO2 thin film. The photodecomposition of benzene on both types of TiO2 films follows the first-order kinetics while the CO(2) and CO formation followed the zero-order kinetics. GC/MS identification of the intermediates produced during the photodegradation of benzene revealed that doping lanthanum into TiO2 thin film favors a cleavage of benzene ring. An optimal lanthanum amount with respect to photocatalytic activity was about 2.5 wt% (La2O3/TiO2).

  10. Structural properties of Fe-doped lanthanum gallate

    NASA Astrophysics Data System (ADS)

    Mori, Kazuhiro; Fukunaga, Toshiharu; Shibata, Koji; Iwase, Kenji; Harjo, Stefanus; Hoshikawa, Akinori; Itoh, Keiji; Kamiyama, Takashi; Ishigaki, Toru

    2004-10-01

    Structural characteristics of Fe-doped LaGaO3-δ were studied by differential scanning calorimeter, neutron and high-temperature X-ray powder diffraction measurements. It was found that a phase transition temperature increases in proportion to an amount of Fe. The crystal structure could be described as a low-temperature orthorhombic phase (Pnma) and a high-temperature rhombohedral one (R 3 bar c), respectively. Lattice parameters and bond lengths between M (=Ga/Fe) and O are monotonically expand with increasing Fe-content on both orthorhombic and rhombohedral phases. This means that a substitution of Ga3+ with Fe3+ leads to an electronic configuration of t2g3eg2 (high-spin state, HS).

  11. Optical, luminescent and laser properties of highly transparent ytterbium doped yttrium lanthanum oxide ceramics

    NASA Astrophysics Data System (ADS)

    Ivanov, M.; Kopylov, Yu.; Kravchenko, V.; Li, Jiang; Pan, Yubai; Kynast, U.; Leznina, M.; Strek, W.; Marciniak, Lukasz; Palashov, O.; Snetkov, I.; Mukhin, I.; Spassky, D.

    2015-12-01

    This paper describes the fabrication and investigation of highly transparent Yb-doped yttrium lanthanum oxide ceramics. For sintering of the ceramics we used a technology, which consists of several consecutive steps: (a) synthesis of weakly agglomerated nanopowder by laser ablation, (b) compacting of the green body with cold isostatic pressing (CIP), and (c) sintering in vacuum. After calcinations of the synthesized nanopowder at 1200 °C, a pure single-phase solid solution Yb3+:(LaxY1-x)2O3 was formed. The lanthanum ions proved to be a good aid to sinter yttria ceramics doped with Yb3+ at comparatively moderate temperatures of about 1650 °C. The ceramics have a relative density higher than 99.99% and grain sizes around 40 μm. The absorption coefficient of 3.2 mm thick Yb0.12La0.27Y1.61O3 ceramics is 0.01 cm-1 at 1150 nm. Laser oscillation at a wavelength of 1033 nm is demonstrated.

  12. Electromechanical properties of lanthanum-doped lead hafnate titanate thin films for integrated piezoelectric MEMS applications

    NASA Astrophysics Data System (ADS)

    Kügeler, C.; Böttger, U.; Schneller, T.

    2009-03-01

    This paper focuses on the deposition and electromechanical characterization of lanthanum-doped lead hafnate titanate (PLHT) thin films as key material in piezoelectric microelectromechanical systems (pMEMS). PLHT ( x/30/70) and PLHT( x/45/55) films with a thickness between 150 nm and 250 nm were deposited by chemical solution deposition (CSD). Thereby x varies between 0 and 10% La content. The electrical characterization shows that undoped ( x=0) PLHT exhibit ferroelectric behavior similar to PZT of the same composition. La doping results in reduced ferroelectric properties and also affects the electromechanical properties. Measurements using a double beam laser interferometer yield a piezoelectric coefficient d 33 of 60 pm/V, which stays constant with an increasing electric field. This leads to a linear displacement compared to undoped PLHT or conventional PZT films used for MEMS applications.

  13. Optical and magnetic properties of zinc oxide quantum dots doped with cobalt and lanthanum.

    PubMed

    Yu, Shiyong; Zhao, Jing; Su, Hai-Quan

    2013-06-01

    Cobalt and Lanthanum-doped ZnO QDs are synthesized by a modified sol-gel method under atmospheric conditions. The as-prepared quantum dots are characterized by X-ray powder diffraction (XRD), energy dispersive X-ray (EDX) analysis and high resolution transmission electron microscopy (HRTEM). The optical properties of the products are studied by fluorescent spectroscopy. With a proper Co and La doping, these nanoparticles possess exceptionally small size and enhanced fluorescence. Hysteresis loops of un-doped ZnO QDs and Co and La-doped ZnO QDs indicate that both the samples show ferromagnetic behavior at room temperature. Finally, these nanoparticles can label the BGC 803 cells successfully in short time and present no evidence of toxicity or adverse affect on cell growth even at the concentration up to 1 mM. We expect that the as-prepared Co and La-doped ZnO QDs can provide a better reliability of the collected data and find promising applications in biological, medical and other fields.

  14. Structures, Stabilities, and Electronic Properties for Rare-Earth Lanthanum Doped Gold Clusters

    NASA Astrophysics Data System (ADS)

    Zhao, Ya-Ru

    2015-02-01

    The structures, stabilities, and electronic properties of rare-earth lanthanum doped gold La2Aun (n = 1-9) and pure gold Aun (n ≤ 11) clusters have been investigated by using density functional theory. The optimized geometries show that the lowest energy structures of La2Aun clusters favour the 3D structure at n ≥ 3. The lanthanum atoms can strongly enhance the stabilities of gold clusters and tend to occupy the most highly coordinated position. By analysing the gap, vertical ionization potential, and chemical hardness, it is found that the La2Au6 isomer possesses higher stability for small-sized La2Aun clusters (n = 1-9). The charges in the La2Aun clusters transfer from La atoms to the Aun host. In addition, Wiberg bond indices analysis reveals that the intensity of different bonds of La2Aun clusters exhibits a sequence of La-La bond > La-Au bond > Au-Au bond.

  15. Effect of CO2 on the stability of strontium doped lanthanum manganite cathode

    NASA Astrophysics Data System (ADS)

    Hu, Boxun; Mahapatra, Manoj K.; Keane, Michael; Zhang, Heng; Singh, Prabhakar

    2014-12-01

    Strontium doped lanthanum manganite cathode stability in 0-10% carbon dioxide containing air has been studied in the temperature range of 1023-1123 K with cathodic biases of 0 V and 0.5 V. The current density of the LSM cathode remains stable after an initial decrease. Surface analyses of the pre-test and post-test LSM cathodes using Auger electron spectroscopy (AES) and attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR) techniques suggest that the formation of SrCO3 at the LSM surface leads to initial performance degradation. Our observations also indicate that CO2 does not affect the current density after an initial LSM activation in air. Overall, the LSM performance degradation in CO2-containing air is less severe than in humidified air.

  16. Synthesis of hexagonal lanthanum germanate apatites through site selective isovalent doping with yttrium

    SciTech Connect

    Kendrick, E.; Slater, P.R.

    2008-08-04

    Apatite-type lanthanum silicates/germanates have been attracting considerable interest as a new class of oxide ion conductors, whose conductivity is mediated by oxide ion interstitials. For the germanates, it has been shown that, depending on composition, the cell can be either hexagonal or triclinic, with evidence for reduced low-temperature conductivities for the latter, attributed to increased defect trapping in this lower symmetry cell. In this paper we show that site selective doping of Y into the triclinic apatite-type oxide ion conductors, La{sub 9.33+z}(GeO{sub 4}){sub 6}O{sub 2+3z/2} (0.33 {<=} z {<=} 0.67) results in a hexagonal lattice for the complete series with correspondingly enhanced low-temperature conductivity.

  17. Influence of Lanthanum Doping on the Structural and Optical Properties of Hematite Nanopowders

    NASA Astrophysics Data System (ADS)

    Justus, J. Sharmila; Dharma Roy, S. Dawn; Raj, A. Moses Ezhil

    2016-10-01

    Rare-earth elements are an attractive class of dopant elements, as they give easily trivalent cations that possibly altering the structure and other properties of the parent nanoparticles and creating multifunctional materials because of their f-electronic configurations. Herein, experimental evidence has been given for a better understanding of the factors that dictate the interactions of La doping on the structure and optical properties of iron oxide nanoparticles. For that, lanthanum doped hematite (α-Fe2O3) nanoparticles were prepared by a facile solution method using iron (III) chloride (FeCl3) as starting precursor and sodium hydroxide (NaOH) as reducing agent without templates at low temperature. As-prepared powders were subsequently calcined in air for 3 hr at 800 °C. Xray diffraction (XRD) technique was used to study the nanocrystal formation of α-Fe2O3 and Fourier Transform Raman (FT-Raman) spectral information identified the chemical bond structure of the nanoparticles. Morphology study of the nanoparticles was identified using Scanning Electron Microscope (SEM) and the incorporated La content was recognized from the Energy Dispersive X-ray Spectroscopy (EDS) analysis. The optical absorption spectrum was recorded in the wavelength range of 200-2000 nm and the optical parameters such as absorption coefficient and optical band gap energy of pure and doped Fe2O3 nanoparticles were determined. Obtained results are interpreted by considering the impregnation of trivalent La cations that replaced Fe cations of the host structure.

  18. Microstructure evolution and electrical characterization of Lanthanum doped Barium Titanate (BaTiO3) ceramics

    NASA Astrophysics Data System (ADS)

    Billah, Masum; Ahmed, A.; Rahman, Md. Miftaur; Mahbub, Rubbayat; Gafur, M. A.; Bashar, M. Shahriar

    2016-07-01

    In the current work, we investigated the structural and dielectric properties of Lanthanum oxide (La2O3) doped Barium Titanate (BaTiO3) ceramics and established a correlation between them. Solid state sintering method was used to dope BaTiO3 with 0.3, 0.5 and 0.7 mole% La2O3 under different sintering parameters. The raw materials used were La2O3 nano powder of ~80nm grain size and 99.995% purity and BaTiO3 nano powder of 100nm grain size and 99.99% purity. Grain size distribution and morphology of fracture surface of sintered pellets were examined by Field Emission Scanning Electron Microscope and X-Ray Diffraction analysis was conducted to confirm the formation of desired crystal structure. The research result reveal that grain size and electrical properties of BaTiO3 ceramic significantly enhanced for small amount of doping (up to 0.5 mole% La2O3) and then decreased with increasing doping concentration. Desired grain growth (0.80-1.3 µm) and high densification (<90% theoretical density) were found by proper combination of temperature, sintering parameters and doping concentration. We found the resultant stable value of dielectric constant was 10000-12000 at 100-300 Hz in the temperature range of 30°-50° C for 0.5 mole% La2O3 with corresponding shift of curie temperature around 30° C. So overall this research showed that proper La3+ concentration can control the grain size, increase density, lower curie temperature and hence significantly improve the electrical properties of BaTiO3 ceramics.

  19. Lanthanum and zirconium co-doped ZnO nanocomposites: synthesis, characterization and study of photocatalytic activity.

    PubMed

    Moafi, Hadi Fallah; Zanjanchi, Mohammad Ali; Shojaie, Abdollah Fallah

    2014-09-01

    Nanocomposits of zinc oxide co-doped with lanthanum and zirconium were prepared using the modified sol-gel method. The samples were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), energy dispersive spectroscopy (EDS), diffuse reflectance spectroscopy (DRS), and BET surface area measurement. For comparison, the La and Zr mono doped ZnO have also been prepared under the same conditions. The XRD results revealed that all the materials showed a hexagonal wurtzite crystal structure. It was found that the particle size of La-Zr-doped ZnO is much smaller as compared to that of pure ZnO. The effect of operational parameters such as, doping concentration, catalyst loading, pH and initial concentration of methylene blue on the extent of degradation was investigated. The photocatalytic activity of the undoped ZnO, mono-doped and La-Zr-ZnO photocatalysts was evaluated by the photocatalytic degradation of methylene blue in aqueous solution. The presence of lanthanium and/or zirconium causes a red shift in the absorption band of ZnO. The results show that the photocatalytic activity of the La-Zr-ZnO photocatalyst is much higher than that of undoped and mono-doped ZnO, resulting from the La and Zr synergistic effect. The co-operation of the lanthanum and zirconium ion leads to the narrowing of the band gap and greatly improves the photocatalytic activity. The photocatalyst co-doped with lanthanum and zirconium 4 mol% shows the best photoactivity and photodecomposition efficiencies were improved by 92% under UV-Vis irradiation at the end of 30 min, compared with the pure and mono doped samples.

  20. Engineered hydrochar composites for phosphorus removal/recovery: Lanthanum doped hydrochar prepared by hydrothermal carbonization of lanthanum pretreated rice straw.

    PubMed

    Dai, Lichun; Wu, Bo; Tan, Furong; He, Mingxiong; Wang, Wenguo; Qin, Han; Tang, Xiaoyu; Zhu, Qili; Pan, Ke; Hu, Qichun

    2014-06-01

    Engineered hydrochar composites (EHC) were synthesized by hydrothermal carbonization (HTC) of lanthanum pretreated rice straw. The as-prepared composite with about 30% lanthanum content showed greater P removal potential than La(OH)3, indicating the synergistic effect of hydrochar and lanthanum in P removal. The adsorption results showed that EHC showed great P adsorption capacities (>50mgPg(-1)) in the pH range of 2.5-10.5, and the presence of competing anions had little negative effects on P adsorption on EHC. The equilibrium time for P adsorption on EHC was considerably reduced under acid condition (12h) compared to alkaline condition (48h). The maximum adsorption capacity was 61.57mgPg(-1) according to Langmuir isotherms. These results suggested that EHC was highly effective in P adsorption in a wide range of pH and the presence of competing anions, thus EHC could be a promising adsorbent for phosphorus removal/recovery from wastewater.

  1. Doped Yttrium Chromite-Ceria Composite as a Redox-Stable and Sulfur-Tolerant Anode for Solid Oxide Fuel Cells

    SciTech Connect

    Yoon, Kyung J.; Coyle, Christopher A.; Marina, Olga A.

    2011-12-11

    A Ca- and Co-doped yttrium chromite (YCCC) - samaria-doped ceria (SDC) composite was studied in relation to a potential use as a solid oxide fuel cell (SOFC) anode material. Tests performed using the yttria-stabilized zirconia (YSZ) electrolyte-supported cells revealed that the electrocatalytic activity of the YCCC-SDC anode towards hydrogen oxidation at 800 C was comparable to that of the Ni-YSZ anode. In addition, the YCCC-SDC anode exhibited superior sulfur tolerant characteristics showing less than 10% increase in a polarization resistance, fully reversible, upon exposure to 20 ppm H2S at 800 C. No performance degradation was observed during multiple reduction-oxidation (redox) cycles when the anode was intentionally exposed to the air environment followed by the reduction in hydrogen. The redox tolerance of the YCCC-SDC anode was attributed to the dimensional and chemical stability of the YCCC exhibiting minimal isothermal chemical expansion upon redox cycling.

  2. White light emission of dysprosium doped lanthanum calcium phosphate oxide and oxyfluoride glasses

    NASA Astrophysics Data System (ADS)

    Luewarasirikul, N.; Kim, H. J.; Meejitpaisan, P.; Kaewkhao, J.

    2017-04-01

    Lanthanum calcium phosphate oxide and oxyfluoride glasses doped with dysprosium oxide were prepared by melt-quenching technique with chemical composition 20La2O3:10CaO:69P2O5:1Dy2O3 and 20La2O3:10CaF2:69P2O5:1Dy2O3. The physical, optical and luminescence properties of the glass samples were studied to evaluate their potential to using as luminescence materials for solid-state lighting applications. The density, molar volume and refractive index of the glass samples were carried out. The optical and luminescence properties were studied by investigating absorption, excitation, and emission spectra of the glass samples. The absorption spectra were investigated in the UV-Vis-NIR region from 300 to 2000 nm. The excitation spectra observed under 574 nm emission wavelength showed the highest peak centered at 349 nm (6H15/2 → 6P7/2). The emission spectra, excited with 349 nm excitation wavelength showed two major peaks corresponding to 482 nm blue emission (4F9/2 → 6H15/2) and 574 nm yellow emission (4F9/2 → 6H13/2). The experimental lifetime were found to be 0.539 and 0.540 for oxide and oxyfluoride glass sample, respectively. The x,y color coordinates under 349 nm excitation wavelength were (0.38, 0.43) for both glass samples, that be plotted in white region of CIE 1931 chromaticity diagram. The CCT values obtained from the glass samples are 4204 K for oxide glass and 4228 K for oxyfluoride glass corresponding to the commercial cool white light (3100-4500 K). Judd-Ofelt theory had also been employed to obtain the J-O parameters (Ω2, Ω4 and Ω6), oscillator strength, radiative transition possibility, stimulated emission cross section and branching ratio. The Ω2 > Ω4 > Ω6 trend of J-O parameters of both glass samples may indicate the good quality of a glass host for using as optical device application. Temperature dependence of emission spectra was studied from 300 K to 10 K and found that the intensity of the emission peak was found to be increased with

  3. High-temperature superconductivity in space-charge regions of lanthanum cuprate induced by two-dimensional doping

    NASA Astrophysics Data System (ADS)

    Baiutti, F.; Logvenov, G.; Gregori, G.; Cristiani, G.; Wang, Y.; Sigle, W.; van Aken, P. A.; Maier, J.

    2015-10-01

    The exploitation of interface effects turned out to be a powerful tool for generating exciting material properties. Such properties include magnetism, electronic and ionic transport and even superconductivity. Here, instead of using conventional homogeneous doping to enhance the hole concentration in lanthanum cuprate and achieve superconductivity, we replace single LaO planes with SrO dopant planes using atomic-layer-by-layer molecular beam epitaxy (two-dimensional doping). Electron spectroscopy and microscopy, conductivity measurements and zinc tomography reveal such negatively charged interfaces to induce layer-dependent superconductivity (Tc up to 35 K) in the space-charge zone at the side of the planes facing the substrate, where the strontium (Sr) profile is abrupt. Owing to the growth conditions, the other side exhibits instead a Sr redistribution resulting in superconductivity due to conventional doping. The present study represents a successful example of two-dimensional doping of superconducting oxide systems and demonstrates its power in this field.

  4. Electrical Conductivity and Chemical Diffusion Coefficient of Strontium-Doped Lanthanum Manganites

    NASA Astrophysics Data System (ADS)

    Yasuda, Isamu; Hishinuma, Masakazu

    1996-05-01

    Electrical conductivity and chemical diffusion coefficient of Sr-doped lanthanum manganites, La 1- xSr xMnO 3±δ( x= 0.05 - 0.20), were measured by the dc four-probe technique and relaxation type experiments where a sudden change of oxygen chemical potential was imposed on the pre-equilibrated sample and the change of electrical conductivity was followed as a function of elapsed time. A defect model is proposed to elucidate the oxygen partial pressure dependence of the measured conductivity and the reported oxygen nonstoichiometry. The transient conductivity behavior after an abrupt change of oxygen partial pressure was successfully described by a diffusion model with consideration of partial control by surface reaction. The determined chemical diffusion coefficients, of the order of 10 -5to 10 -4cm 2s -1at 1000°C, increased with decreased oxygen partial pressure due to the thermodynamic enhancement effect. Using the enhancement factor estimated by combination of the proposed defect model and the ambipolar diffusion theory, the oxygen vacancy diffusion coefficients were derived. High vacancy diffusivity comparable to that of Fe- or Co-based perovskites predicts fast oxide ion diffusion under conditions where the manganites show oxygen deficient type non-stoichiometry.

  5. Cationic Redistribution at Epitaxial Interfaces in Superconducting Two-Dimensionally Doped Lanthanum Cuprate Films.

    PubMed

    Baiutti, Federico; Gregori, Giuliano; Wang, Yi; Suyolcu, Y Eren; Cristiani, Georg; van Aken, Peter A; Maier, Joachim; Logvenov, Gennady

    2016-10-12

    The exploration of interface effects in complex oxide heterostructures has led to the discovery of novel intriguing phenomena in recent years and has opened the path toward the precise tuning of material properties at the nanoscale. One recent example is space-charge superconductivity. Among the complex range of effects which may arise from phase interaction, a crucial role is played by cationic intermixing, which defines the final chemical composition of the interface. In this work, we performed a systematic study on the local cationic redistribution of two-dimensionally doped lanthanum cuprate films grown by oxide molecular beam epitaxy, in which single LaO layers in the epitaxial crystal structure were substituted by layers of differently sized and charged dopants (Ca, Sr, Ba, and Dy). In such a model system, in which the dopant undergoes an asymmetric redistribution across the interface, the evolution of the cationic concentration profile can be effectively tracked by means of atomically resolved imaging and spectroscopic methods. This allowed for the investigation of the impact of the dopant chemistry (ionic size and charge) and of the growth conditions (temperature) on the final superconducting and structural properties. A qualitative model for interface cationic intermixing, based on thermodynamic considerations, is proposed. This work highlights the key role which cationic redistribution may have in the definition of the final interface properties and represents a further step forward the realization of heterostructures with improved quality.

  6. Dynamic Nuclear Polarization in Samarium Doped Lanthanum Magnesium Nitrate. Ph.D. Thesis - Va. Polytechnic Inst.

    NASA Technical Reports Server (NTRS)

    Byvik, C. E.

    1971-01-01

    The dynamic nuclear polarization of hydrogen nuclei by the solid effect in single crystals of samarium doped lanthanum magnesium nitrate (Sm:LMN) was studied theoretically and experimentally. The equations of evolution governing the dynamic nuclear polarization by the solid effect were derived in detail using the spin temperature theory and the complete expression for the steady state enhancement of the nuclear polarization was calculated. Experimental enhancements of the proton polarization were obtained for eight crystals at 9.2 GHz and liquid helium temperatures. The samarium concentration ranged from 0.1 percent to 1.1 percent as determined by X-ray fluorescence. A peak enhancement of 181 was measured for a 1.1 percent Sm:LMN crystal at 3.0 K. The maximum enhancements extrapolated with the theory using the experimental data for peak enhancement versus microwave power and correcting for leakage, agree with the ideal enhancement (240 in this experiment) within experimental error for three of the crystals.

  7. Probing highly luminescent europium-doped lanthanum orthophosphate nanorods for strategic applications.

    PubMed

    Saraf, Mohit; Kumar, Pawan; Kedawat, Garima; Dwivedi, Jaya; Vithayathil, Sajna Antony; Jaiswal, Nagendra; Kaipparettu, Benny Abraham; Gupta, Bipin Kumar

    2015-03-16

    Herein we have established a strategy for the synthesis of highly luminescent and biocompatible europium-doped lanthanum orthophosphate (La0.85PO4Eu0.15(3+)) nanorods. The structure and morphogenesis of these nanorods have been probed by XRD, SEM, and TEM/HRTEM techniques. The XRD result confirms that the as-synthesized nanorods form in a monazite phase with a monoclinic crystal structure. Furthermore, the surface morphology shows that the synthesized nanorods have an average diameter of ∼90 nm and length of ∼2 μm. The HRTEM images show clear lattice fringes that support the presence of better crystal quality and enhanced photoluminescence hypersensitive red emission at 610 nm ((5)D0-(7)F2) upon 394 nm wavelength excitation. Furthermore, time-resolved spectroscopy and an MTT assay of these luminescent nanorods demonstrate a photoluminescent decay time of milliseconds with nontoxic behavior. Hence, these obtained results suggest that the as-synthesized luminescent nanorods could be potentially used in invisible security ink and high-contrast bioimaging applications.

  8. Synthesis, structural, optical and Raman studies of pure and lanthanum doped ZnSe nanoparticles

    SciTech Connect

    Kumar, Pushpendra; Singh, Jai; Pandey, Mukesh Kumar; Jeyanthi, C.E.; Siddheswaran, R.; Paulraj, M.; Hui, K.N.; Hui, K.S.

    2014-01-01

    Graphical abstract: - Highlights: • Template-free synthesis of ZnSe and ZnSe:La nanoparticles was developed at low temperature 100 °C. • Cubic ZnSe and ZnSe:La nanoparticles were obtained by chemical route. • As-synthesized ZnSe:La nanoparticles showed higher emission intensity than ZnSe nanoparticles. • Band gap (E{sub g}) of ZnSe nanoparticles was bigger than ZnSe nanoparticles due to nanosized effect. - Abstract: In this work, a simple, effective and reproducible chemical synthetic route for the production of high-quality, pure ZnSe nanoparticles (NPs), and lanthanum-doped ZnSe (ZnSe:La) NPs is presented. The wide bandgap, luminescent pure ZnSe and ZnSe:La NPs has been synthesized at a low temperature (100 °C) in a single template-free step. The size and optical bandgap of the NPs was analyzed from powder X-ray diffraction (XRD), UV–visible (UV–vis) spectroscopy, transmission electron microscopy (TEM), and high resolution transmission electron microscopy (HRTEM). A broad photoluminescence (PL) emission across the visible spectrum has been demonstrated by a systematic blue-shift in emission due to the formation of small nanoparticles. Here, contribution to emission intensity from surface states of NPs increases with La doping. TEM data revealed that the average size of ZnSe and ZnSe:La NPs is 14 and 8 nm, respectively. On the other hand, band gap energy E{sub g} of ZnSe and ZnSe:La NPs were found to be 3.59 eV and 3.65 eV, respectively. Results showed that hydrazine hydrate played multiple roles in the formation of ZnSe and ZnSe:La NPs. A possible reaction mechanism for the growth of NPs is also discussed.

  9. Enhanced ionic conductivity of apatite-type lanthanum silicate electrolyte for IT-SOFCs through copper doping

    NASA Astrophysics Data System (ADS)

    Ding, Xifeng; Hua, Guixiang; Ding, Dong; Zhu, Wenliang; Wang, Hongjin

    2016-02-01

    Apatite-type Lanthanum silicate (LSO) is among the most promising electrolyte for intermediate temperature solid oxide fuel cells (IT-SOFCs) owing to the high conductivity and low activation energy at lower temperature than traditional doped-zirconia electrolyte. The ionic conductivity as well as the sintering density of lanthanum silicate oxy-apatite, La10Si6-xCuxO27-δ (LSCO, 0 ≤ x ≤ 2), was effectively enhanced through a small amount of doped copper. The phase composition, relative density, ionic conductivity and thermal expansion behavior of La10Si6-xCuxO27-δ was systematically investigated by X-ray diffraction (XRD), Archimedes' drainage method, scanning electron microscope (SEM), electrochemical impedance spectra (EIS) and thermal dilatometer techniques. With increasing copper doping content, the ionic conductivity of La10Si6-xCuxO27-δincreased, reaching a maximum of 4.8 × 10-2 S cm-1 at 800 °C for x = 1.5. The improved ionic conductivity could be primarily associated with the enhanced grain conductivity. The power output performance of NiO-LSCO/LSCO/LSCF single cell was superior to that obtained on NiO-LSO/LSO/LSCF at different temperatures using hydrogen as fuel and oxygen as oxidant, which could be attributed to the enhanced oxygen ionic conductivity as well as the sintering density for the copped doped lanthanum silicate. In conclusion, the apatite La10Si4.5Cu1.5O25.5 is a promising candidate electrolyte for IT-SOFCs.

  10. [Study on preparation of lanthanum-doped TiO2 nanometer thin film materials and its photocatalytic activity].

    PubMed

    Zheng, Huai-li; Tang, Ming-fang; Gong, Ying-kun; Deng, Xiao-jun; Wu, Bang-hua

    2003-04-01

    In this paper, lanthanum-doped TiO2 nanometer film materials coated on glass were prepared in Ti(OBu)4 precursor solutions by sol-gel processing. Transmittance and photocatalytic activity were respectively investigated and tested for these nanometer thin films prepared with different amount of lanthanum (La), different amount of polyethylene glycol (PEG), and different coating layer times. Some reactive mechanisms were also discussed. For one layer La-addition had little effect on the film transmissivity; but the photocatalytic activity was significantly improved due to La-addition. With increasing PEG, the transmittance of the film decreased for one layer film; but its photocatalytic activity did not rise. Increasing layer number did not affect the transmissivity of multilayer film. After coating two times, increasing layer number did not significantly improve the photocatalytic activity. The highest photocatalytic activity and best transmissivity were obtained for two layer TiO2 film when the dosage of lanthanum was 0.5 g and the dosage of polyethylene was 0.2 g in the precursor solutions. These materials will probably be used in the protection of environment, waste water treatment, and air purification.

  11. Doped lanthanum nickelates with a layered perovskite structure as bifunctional cathode catalysts for rechargeable metal-air batteries.

    PubMed

    Jung, Kyu-Nam; Jung, Jong-Hyuk; Im, Won Bin; Yoon, Sukeun; Shin, Kyung-Hee; Lee, Jong-Won

    2013-10-23

    Rechargeable metal-air batteries have attracted a great interest in recent years because of their high energy density. The critical challenges facing these technologies include the sluggish kinetics of the oxygen reduction-evolution reactions on a cathode (air electrode). Here, we report doped lanthanum nickelates (La2NiO4) with a layered perovskite structure that serve as efficient bifunctional electrocatalysts for oxygen reduction and evolution in an aqueous alkaline electrolyte. Rechargeable lithium-air and zinc-air batteries assembled with these catalysts exhibit remarkably reduced discharge-charge voltage gaps (improved round-trip efficiency) as well as high stability during cycling.

  12. Glass-Like Thermal Conductivity of (010)-Textured Lanthanum-Doped Strontium Niobate Synthesized with Wet Chemical Deposition

    DOE PAGES

    Foley, Brian M.; Brown-Shaklee, Harlan J.; Campion, Michael J.; ...

    2014-11-08

    We have measured the cross-plane thermal conductivity (κ) of (010)-textured, undoped, and lanthanum-doped strontium niobate (Sr2-xLaxNb2O7-δ) thin films via time-domain thermoreflectance. Then the thin films were deposited on (001)-oriented SrTiO3 substrates via the highly-scalable technique of chemical solution deposition. We find that both film thickness and lanthanum doping have little effect on κ, suggesting that there is a more dominant phonon scattering mechanism present in the system; namely the weak interlayer-bonding along the b-axis in the Sr2Nb2O7 parent structure. We also compare our experimental results with two variations of the minimum-limit model for κ and discuss the nature of transportmore » in material systems with weakly-bonded layers. The low cross-plane κ of these scalably-fabricated films is comparable to that of similarly layered niobate structures grown epitaxially.« less

  13. Glass-Like Thermal Conductivity of (010)-Textured Lanthanum-Doped Strontium Niobate Synthesized with Wet Chemical Deposition

    SciTech Connect

    Foley, Brian M.; Brown-Shaklee, Harlan J.; Campion, Michael J.; Medlin, Douglas L.; Clem, Paul G.; Ihlefeld, Jon F.; Hopkins, Patrick E.

    2014-11-08

    We have measured the cross-plane thermal conductivity (κ) of (010)-textured, undoped, and lanthanum-doped strontium niobate (Sr2-xLaxNb2O7-δ) thin films via time-domain thermoreflectance. Then the thin films were deposited on (001)-oriented SrTiO3 substrates via the highly-scalable technique of chemical solution deposition. We find that both film thickness and lanthanum doping have little effect on κ, suggesting that there is a more dominant phonon scattering mechanism present in the system; namely the weak interlayer-bonding along the b-axis in the Sr2Nb2O7 parent structure. We also compare our experimental results with two variations of the minimum-limit model for κ and discuss the nature of transport in material systems with weakly-bonded layers. The low cross-plane κ of these scalably-fabricated films is comparable to that of similarly layered niobate structures grown epitaxially.

  14. Optical and transport properties of lanthanum-doped stannate BaSnO3

    NASA Astrophysics Data System (ADS)

    Hadjarab, B.; Bouguelia, A.; Trari, M.

    2007-10-01

    BaSnO3 crystallizes in a cubic perovskite structure and exhibits insulating behaviour. It can be made conducting by reducing a small fraction of Sn4+ into Sn2+ under an O2-free atmosphere. This can be achieved through the solid solution Ba1-xLaxSnO3-δ which is a mixed phase for x > 0.02, behaviour readily understood in terms of the lone pair cation Sn2+. The magnetic susceptibility was measured down to 4.2 K and is less than 1.7 × 10-5 emu cgs mol-1 consistent with collective electron behaviour. The Mössbauer spectrum exhibits a wide unsplit peak with a quadrupole doublet of 3.18 mm s-1 and an isomer shift of 0.12 mm s-1 characteristic of Sn4+and corroborating the delocalization of the stereo chemical pair 5s2. The band gap Eg was found to be 3.12 eV; further indirectly allowed inter-band transition occurs at 2.85 eV. The transport properties of Ba0.98La0.02SnO3-δ indicate n-type conductivity (σ300 K = 4.03 Ω-1 cm-1), little temperature dependence, with an activation energy ΔE of ~1 meV and an electron mobility μ300 K ~ 0.1 cm2 V-1 s-1, thermally activated. The conduction occurs by small polaron hopping between mixed valence Sn4+/2+ ions. The observed conductivity is greater than that coming from La-substitution with one-electron doping implying the existence of oxygen vacancies. The electrons are believed to travel in the Sn-5s conduction band with an effective mass of 3.7 mo. The non-linear dependence of Ln σ versus T-1 at low temperatures could result from a predominant variable range hopping as suggested by the linear variation of log σ versus T-0.25. The electron localization may be attributed to the random distribution of lanthanum as well as oxygen vacancies.

  15. High-temperature superconductivity in space-charge regions of lanthanum cuprate induced by two-dimensional doping.

    PubMed

    Baiutti, F; Logvenov, G; Gregori, G; Cristiani, G; Wang, Y; Sigle, W; van Aken, P A; Maier, J

    2015-10-20

    The exploitation of interface effects turned out to be a powerful tool for generating exciting material properties. Such properties include magnetism, electronic and ionic transport and even superconductivity. Here, instead of using conventional homogeneous doping to enhance the hole concentration in lanthanum cuprate and achieve superconductivity, we replace single LaO planes with SrO dopant planes using atomic-layer-by-layer molecular beam epitaxy (two-dimensional doping). Electron spectroscopy and microscopy, conductivity measurements and zinc tomography reveal such negatively charged interfaces to induce layer-dependent superconductivity (Tc up to 35 K) in the space-charge zone at the side of the planes facing the substrate, where the strontium (Sr) profile is abrupt. Owing to the growth conditions, the other side exhibits instead a Sr redistribution resulting in superconductivity due to conventional doping. The present study represents a successful example of two-dimensional doping of superconducting oxide systems and demonstrates its power in this field.

  16. High-temperature superconductivity in space-charge regions of lanthanum cuprate induced by two-dimensional doping

    PubMed Central

    Baiutti, F.; Logvenov, G.; Gregori, G.; Cristiani, G.; Wang, Y.; Sigle, W.; van Aken, P. A.; Maier, J.

    2015-01-01

    The exploitation of interface effects turned out to be a powerful tool for generating exciting material properties. Such properties include magnetism, electronic and ionic transport and even superconductivity. Here, instead of using conventional homogeneous doping to enhance the hole concentration in lanthanum cuprate and achieve superconductivity, we replace single LaO planes with SrO dopant planes using atomic-layer-by-layer molecular beam epitaxy (two-dimensional doping). Electron spectroscopy and microscopy, conductivity measurements and zinc tomography reveal such negatively charged interfaces to induce layer-dependent superconductivity (Tc up to 35 K) in the space-charge zone at the side of the planes facing the substrate, where the strontium (Sr) profile is abrupt. Owing to the growth conditions, the other side exhibits instead a Sr redistribution resulting in superconductivity due to conventional doping. The present study represents a successful example of two-dimensional doping of superconducting oxide systems and demonstrates its power in this field. PMID:26481902

  17. Study of energy transfer and spectral downshifting in Ce, RE (RE = Nd and Yb) co-doped lanthanum phosphate

    NASA Astrophysics Data System (ADS)

    Sawala, N. S.; Omanwar, S. K.

    2017-03-01

    The phosphors LaPO4 (Lanthanum phosphate) doped with Ce(III)/Ce3+ and co-doped with Ce3+-Nd3+ and Ce3+-Yb3+ were effectively synthesized by conventional solid state reaction method. The prepared samples were characterized by powder X-ray diffraction (XRD) and surface morphology was studied by scanning electronic microscope (SEM). The photoluminescence (PL) properties were studied by spectrophotometers in near infrared (NIR) and ultraviolet visible (UV-VIS) region. Additionally the luminescence time decay curves of samples were investigated to confirm energy transfer (ET) process. The Ce3+-Nd3+ ion co-doped LaPO4 phosphors can convert a photon of UV region (278 nm) into photons of NIR region (1058 nm). While Ce3+-Yb3+ ion doped LaPO4 phosphors convert photons of UV region (278 nm) into photons of NIR region (979 nm). The Ce3+ ion acts like sensitizer and Nd3+/Yb3+ ions act as activators. Both kinds of emissions are suitable for improving spectral response of solar cells.

  18. Synthesis and characterization of UV-treated Fe-doped bismuth lanthanum titanate-doped TiO2 layers in dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Song, Myoung Geun; Bark, Chung Wung

    2016-06-01

    Dye-sensitized solar cells (DSSCs) based on titanium dioxide (TiO2) have been extensively studied because they constitute promising low-cost alternatives to their conventional semiconductor-based counterparts. However, much of the effort aimed at achieving high conversion efficiencies has focused on dye and liquid electrolytes. In this work, we report the photovoltaic characteristics of DSSCs fabricated by mixing TiO2 with Fe-doped bismuth lanthanum titanate (Fe-BLT). These nanosized Fe-BLT powders were prepared by using a high-energy ball-milling process. In addition, we used a UV radiation-ozone (UV-O3) treatment to change the surface wettability of TiO2 from hydrophobic to hydrophilic and thereby prevented the easy separation of the Fe-BLT-mixed TiO2 from the fluorine-doped tin-oxide (FTO) coating glass.

  19. Atomic-absorption determination of rhodium in chromite concentrates

    USGS Publications Warehouse

    Schnepfe, M.M.; Grimaldi, F.S.

    1969-01-01

    Rhodium is determined in chromite concentrates by atomic absorption after concentration either by co-precipitation with tellurium formed by the reduction of tellurite with tin(II) chloride or by fire assay into a gold bead. Interelement interferences in the atomic-absorption determination are removed by buffering the solutions with lanthanum sulphate (lanthanum concentration 1%). Substantial amounts of Ag, Al, Au, Bi, Ca, Cd, Co, Cr, Cu, Fe, Ho, Hg, K, La, Mg, Mn, Mo, Na, Ni, Pb, Te, Ti, V, Y, Zn and platinum metals can be tolerated. A lower limit of approximately 0.07 ppm Rh can be determined in a 3-g sample. ?? 1969.

  20. Stratiform chromite deposit model

    USGS Publications Warehouse

    Schulte, Ruth F.; Taylor, Ryan D.; Piatak, Nadine M.; Seal, Robert R., II

    2010-01-01

    Stratiform chromite deposits are of great economic importance, yet their origin and evolution remain highly debated. Layered igneous intrusions such as the Bushveld, Great Dyke, Kemi, and Stillwater Complexes, provide opportunities for studying magmatic differentiation processes and assimilation within the crust, as well as related ore-deposit formation. Chromite-rich seams within layered intrusions host the majority of the world's chromium reserves and may contain significant platinum-group-element (PGE) mineralization. This model of stratiform chromite deposits is part of an effort by the U.S. Geological Survey's Mineral Resources Program to update existing models and develop new descriptive mineral deposit models to supplement previously published models for use in mineral-resource and mineral-environmental assessments. The model focuses on features that may be common to all stratiform chromite deposits as a way to gain insight into the processes that gave rise to their emplacement and to the significant economic resources contained in them.

  1. Highly active lanthanum doped ZnO nanorods for photodegradation of metasystox.

    PubMed

    Korake, P V; Dhabbe, R S; Kadam, A N; Gaikwad, Y B; Garadkar, K M

    2014-01-05

    La-doped ZnO nanorods with different La contents were synthesized by microwave assisted method and characterized by various sophisticated techniques such as XRD, UV-Vis., EDS, XPS, SEM and TEM. The XRD patterns of the La-doped ZnO indicate hexagonal crystal structure with an average crystallite size of 30nm. It was found that the crystallite size of La-doped ZnO is much smaller as compared to pure ZnO and decreases with increasing La content. The photocatalytic activity of 0.5mol% La-doped ZnO in the degradation of metasystox was studied. It was observed that degradation efficiency of metasystox over La-doped ZnO increases up to 0.5mol% doping then decreases for higher doping levels. Among the catalyst studied, the 0.5mol% La-doped ZnO was the most active, showing high photocatalytic activity for the degradation of metasystox. The maximum reduction of concentration of metasystox was observed under static condition at pH 8. Reduction in the Chemical Oxygen Demand (COD) of metasystox was observed after 150min. The cytotoxicological studies of meristematic root tip cells of Allium cepa were studied. The results obtained indicate that photocatalytically degraded products of metasystox were less toxic as compared to metasystox.

  2. The effect of induced strains on the optical band gaps in lanthanum-doped zinc ferrite nanocrystalline powders

    NASA Astrophysics Data System (ADS)

    Hamed, Fathalla; Ramachandran, Tholkappiyan; Kurapati, Vishista

    2016-07-01

    ZnFe1.96La0.04O4 nanocrystalline powders were synthesized by auto-combustion with the aid of glycine as fuel. The synthesized powders were subjected to heat treatment in air at constant temperatures (600-970∘C) for a period of 2 h. The annealed powders were characterized by X-ray diffraction (XRD), Fourier transformation infrared spectroscopy (FTIR), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS) and UV-Vis-NIR spectroscopy. The as-synthesized and annealed powders formed spongy porous network structure with voids and pores. All the powders were found to be single phase nanomaterial with cubic spinel crystal structure and the desired composition; however, they contained strains, dislocations and lattice distortions. Some of these strains and dislocations are relaxed as a function of annealing temperature. The powders displayed direct and indirect optical band gaps. The energies of these band gaps were found to vary as a function of the induced strains and dislocations. It is suggested that the energy of the optical band gap in lanthanum-doped zinc ferrite nanocrystalline powders can be varied as a function of induced strains if the initial preparation conditions and the following heat treatments are controlled.

  3. Mitigating voltage and capacity fading of lithium-rich layered cathodes by lanthanum doping

    NASA Astrophysics Data System (ADS)

    Yu, Ruizhi; Wang, Gang; Liu, Meihong; Zhang, Xiaohui; Wang, Xianyou; Shu, Hongbo; Yang, Xiukang; Huang, Weihua

    2016-12-01

    La-doped lithium-rich layered oxide material Li1.2Mn0.54-xNi0.13Co0.13LaxO2 (x = 0.01, 0.02, 0.03) is firstly synthesized via a solvothermal method and subsequent high-temperature calcination technique. The effects of La substitution for partial Mn on the structure and electrochemical performance of materials are systematically studied by inductively coupled plasma optical emission spectroscopy (ICP-OES), field-emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), energy-dispersive X-ray spectroscope (EDS), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy and electrochemical measurement. The results reveal that La is effectively and homogenously doped into the materials, which can expand pathway for intercalation/deintercalation of Li+ ions. In addition, owing to La doping, the Li1.2Mn0.52Ni0.13Co0.13La0.02O2 sample exhibits 93.2% capacity retention after 100 cycles at 1 C. More importantly, this doping can effectively restrain the decrease of average discharge voltage upon cycling, which is one of the longstanding fatal drawbacks for lithium-rich layered oxide material. Moreover, La doping can stabilize the layered framework upon long term cycling and suppress voltage fading, and thus resulting in the better cycling performance. Additionally, the rate capability is also improved by La doping due to the higher diffusion velocity of Li+ ions.

  4. Low-temperature thermoluminescence spectra of rare-earth-doped lanthanum fluoride

    NASA Astrophysics Data System (ADS)

    Yang, B.; Townsend, P. D.; Rowlands, A. P.

    1998-01-01

    Lanthanum fluoride consistently shows two strong thermoluminescence glow peaks at low temperature in pure material near 90 and 128 K. A model is proposed in which these thermoluminescence peaks arise from the annealing of halogen defect sites, similar to the H and Vk centers of the alkali halides. Relaxation and decay of these defects in the pure LaF3 lattice results in broad-band intrinsic luminescence. Addition of rare-earth-impurity ions has two effects. First, the broad-band emission is replaced by narrow-band line emission defined by the trivalent rare-earth dopants. Second, it preferentially determines the formation of the halogen defect sites at impurity lattice sites and such sites appear to increase in thermal stability since the glow peak temperature increases from 128 K in the intrinsic material up to 141 K through the sequence of rare-earth dopants from La to Er. The temperature movement directly correlates with the changes in ionic size of the rare-earth ions, when allowance is made for differences in effective coordination number of the impurity ions. The data suggest two alternative lattice sites can be occupied. The model emphasizes that the intense thermoluminescence signals arise from internal charge rearrangements and annealing of defect complexes, rather than through the more conventional model of separated charge traps and recombination centers. At higher temperatures there is a complex array of glow peaks which depend not only on the dopant concentration but also are specific to each rare earth. Such effects imply defect models giving thermoluminescence within localized complexes and possible reasons are mentioned.

  5. Low-temperature thermoluminescence spectra of rare-earth-doped lanthanum fluoride

    SciTech Connect

    Yang, B.; Townsend, P.D.; Rowlands, A.P.

    1998-01-01

    Lanthanum fluoride consistently shows two strong thermoluminescence glow peaks at low temperature in pure material near 90 and 128 K. A model is proposed in which these thermoluminescence peaks arise from the annealing of halogen defect sites, similar to the H and V{sub k} centers of the alkali halides. Relaxation and decay of these defects in the pure LaF{sub 3} lattice results in broad-band intrinsic luminescence. Addition of rare-earth-impurity ions has two effects. First, the broad-band emission is replaced by narrow-band line emission defined by the trivalent rare-earth dopants. Second, it preferentially determines the formation of the halogen defect sites at impurity lattice sites and such sites appear to increase in thermal stability since the glow peak temperature increases from 128 K in the intrinsic material up to 141 K through the sequence of rare-earth dopants from La to Er. The temperature movement directly correlates with the changes in ionic size of the rare-earth ions, when allowance is made for differences in effective coordination number of the impurity ions. The data suggest two alternative lattice sites can be occupied. The model emphasizes that the intense thermoluminescence signals arise from internal charge rearrangements and annealing of defect complexes, rather than through the more conventional model of separated charge traps and recombination centers. At higher temperatures there is a complex array of glow peaks which depend not only on the dopant concentration but also are specific to each rare earth. Such effects imply defect models giving thermoluminescence within localized complexes and possible reasons are mentioned. {copyright} {ital 1998} {ital The American Physical Society}

  6. Spectroscopic and nonlinear optical studies of pure and Nd-doped lanthanum strontium borate glasses

    NASA Astrophysics Data System (ADS)

    Harde, G. B.; Muley, G. G.

    2016-05-01

    Borate glasses of the system xNd2O3-(1-x) La2O3-SrCO3-10H3BO3 (with x = 0 and 0.05) were prepared by using a convectional melt quenching technique. The amorphous nature of the quenched glasses has been confirmed by powder X-ray diffraction analysis. In order to study the spectroscopic and nonlinear optical properties of fabricated glasses, ultraviolet-visible transmission spectroscopy and open aperture z-scan measurements have been employed. In Nd doped glasses, the transition 4I9/2 → 4G5/2 + 2G7/2 has found more prominent than the other transitions. Optical band gap energies of glasses have been determined and found less for Nd doped glass.

  7. Dielectric relaxation and alternating current conductivity of lanthanum, gadolinium, and erbium-polyvinyl alcohol doped films

    NASA Astrophysics Data System (ADS)

    Hanafy, Taha A.

    2012-08-01

    Fourier transform infrared (FTIR) spectrum dielectric constant, ɛ', loss tangent, tan(δ), electric modulus, M*, and ac conductivity, σac, of pure polyvinyl alcohol (PVA) as well as La-, Gd-, and Er-PVA doped samples have been carried out. The dielectric properties have been studied in the temperature and frequency ranges; 300-450 K and 1 kHz-4 MHz, respectively. FTIR measurements reveal that La3+, Gd3+, and Er3+ ions form complex configuration within PVA structure. Two relaxation processes, namely, ρ and α were observed in pure PVA sample. The first process is due to the interfacial or Maxwell-Wagner-Sillers polarization. The second one is related to the micro-Brownian motion of the main chains. For doped PVA samples, α-relaxation process splits into αa and αc. This splitting is due to the segmental motion in the amorphous (αa) and crystalline (αc) phases of PVA matrix. Electric modulus analysis was discussed to understand the mechanism of the electrical transport process. The behavior of ac conductivity for all PVA samples indicates that the conduction mechanism is correlated barrier hopping.

  8. A first-principles study of co-doping in lanthanum bromide

    NASA Astrophysics Data System (ADS)

    Aberg, Daniel; Sadigh, Babak; Schleife, Andre; Erhart, Paul

    2015-03-01

    It was recently shown that the energy resolution of Ce-doped LaBr3 scintillator radiation detectors can be crucially improved by co-doping with Sr, Ca, or Ba. Here we outline a mechanism for this enhancement on the basis of electronic structure calculations. We show that Sr dopants create and bind to Br vacancies, resulting in stable neutral complexes. The association with Sr causes the deep vacancy level to move toward the conduction band edge. This is essential for reducing the effective carrier density available for Auger quenching during thermalization of hot carriers. Subsequent de-trapping of electrons from the complexes can activate Ce dopants that have previously captured a hole leading to luminescence. This mechanism implies an overall reduction of Auger quenching of free carriers, which is expected to improve the linearity of the photon light yield with respect to the energy of incident electron or photon. Optical properties of the Ce-Sr-vacancy triple complex are discussed and compared to experiment. Prepared by LLNL under Contract DE-AC52-07NA27344. Support from the National Nuclear Security Administration Office of Nonproliferation Research and Development (NA-22) is acknowledged.

  9. Ion beam irradiation of lanthanum and thorium-doped yttrium titanates

    NASA Astrophysics Data System (ADS)

    Lian, J.; Zhang, F. X.; Peters, M. T.; Wang, L. M.; Ewing, R. C.

    2007-05-01

    Y2Ti2O7 pyrochlores doped with La have been sintered at 1373 K for 12 h with the designed compositions of the (LaxY1-x)2Ti2O7 system (x = 0, 0.08, 0.5, and 1), and the phase compositions were analyzed by X-ray diffraction. Limited amounts of La were incorporated into yttrium titanate pyrochlore structure for La-doped samples; while, the end member composition of La2Ti2O7 formed a layered perovskite structure. Ion beam-induced amorphization occurred for all compositions in the (LaxY1-x)2Ti2O7 binary under 1 MeV Kr2+ irradiation at room temperature, and the critical amorphization dose decreased with increasing amounts of La3+. The critical amorphization temperatures for Y2Ti2O7, (La0.162Y0.838)2Ti2O7 and La2Ti2O7 were determined to be ∼780, 890 and 920 K, respectively. Th4+ and Fe3+-doped yttrium titanate pyrochlores were synthesized at 1373 K by sintering Y2Ti2O7 with (ThO2 + Fe2O3). Pyrochlore structures and the chemical compositions were primarily identified by the X-ray diffraction and energy dispersive X-ray (EDX) measurements. The lattice parameter and the critical amorphization dose (1 MeV Kr2+ at room temperature) increase for yttrium titanate pyrochlores with the addition of Th. The increasing 'resistance' to amorphization with less La and greater Th and Fe contents for (Y1-xLax)2Ti2O7 and Y2Ti2O7-Fe2O3-ThO2 systems, respectively, are consistent with the changes in the average ionic radius ratio at the A-sites and B-sites. These results suggest that the addition of lanthanides and actinides (e.g., Th, U, or Pu) will affect the structural stability, as well as the radiation response behavior of the pyrochlore structure-type.

  10. High Temperature Electrical Properties and Defect Structures of Alkaline Earth-Doped Lanthanum Cuprate Superconductors.

    NASA Astrophysics Data System (ADS)

    Shen, Li.

    1995-01-01

    Existing oxygen nonstoichiometry data of rm La_{2-x}Ba_{x}CuO _{4-y} and rm La _{2-x}Sr_{x}CuO_ {4-y} have been fitted by defect structure models featuring isolated oxygen vacancies, neutral associates and singly charged associates, respectively. The associate models fit the data acceptably well up to x = 0.4 while the isolated vacancy model does not fit the data as satisfactorily. Therefore, the oxygen deficiency in both systems is attributed to dopant-vacancy associates rather than isolated oxygen vacancies. However, all three models are unable to reproduce the flattening of electrical properties at high doping levels. Jonker plots reveal that the flattening is caused by degeneracy. The oxygen partial pressure dependence of the electrical properties indicates that the associates are not neutral but singly charged. Thermoelectric power and electrical conductivity have been measured in situ for rm La_ {2-x}Ca_{x}CuO_{4 -y} with x = 0-0.16 in P(O_2 ) = 10^{-5} { -1} atm at T = 700-1000^circ C. The results are similar to those of rm La_{2-x}Ba_{x}CuO _{4-y} and rm La _{2-x}Sr_{x}CuO_ {4-y} yet significant magnitudes of oxygen deficiency reportedly occur in rm La_ {2-x}Ca_{x}CuO_{4 -y} at much lower doping levels. Defect structure models involving charged oxygen vacancies cannot simultaneously fit both properties. Neutral oxygen vacancies and their association with dopants were invoked to reconcile both electrical property and oxygen nonstoichiometry data. The proposed defect structure models have been rationalized based on the bond-length mismatch first observed by Goodenough and his coworkers. The Cu-O bonds in the CuO_2 layers are longer than the La-O bonds in the (LaO)_2 layers. Substitution of larger Ba or Sr for La relieves the mismatch by lengthening the La-O bonds. Holes created for charge compensation contribute to the relief by shortening the Cu-O bonds. Once the mismatch is completely relieved, charged oxygen vacancies are formed in the (LaO)_2 layers, to

  11. Effect of ‘A’-site non stoichiometry in strontium doped lanthanum ferrite based solid oxide fuel cell cathodes

    SciTech Connect

    Banerjee, Koyel; Mukhopadhyay, Jayanta Barman, Madhurima; Basu, Rajendra N.

    2015-12-15

    Highlights: • La{sub 1−x}Sr{sub x}Co{sub y}Fe{sub 1−y}O{sub 3−δ}, x = 0.4; y = 0.2 system varying La-site (0.6–0.54) are studied. • Combustion synthesis technique is used to prepare the powder samples. • Highest electrical conductivity observed with largest A-site deficit composition. • Lowest cathode polarization is found with the same composition (0.02 Ω cm{sup 2}). • Composition with largest A-site deficiency exhibits best performance (2.84 A cm{sup −2}). - Abstract: Effect of A-site non-stoichiometry in strontium doped lanthanum cobalt ferrite (La{sub 1−x}Sr{sub x}Co{sub y}Fe{sub 1−y}O{sub 3−δ}, x = 0.4; y = 0.2) is studied in a systematic manner with variation of ‘A’ site stoichiometry from 1 to 0.94. The perovskite based cathode compositions are synthesized by combustion synthesis. Powder characterizations reveal rhombohedral crystal structure with crystallite size ranging from 29 to 34 nm with minimum lattice spacing of 0.271 nm. Detailed sintering studies along with total DC electrical conductivities are evaluated in the bulk form with variation of sintering temperatures. The electrode polarizations are measured in the symmetric cell configuration by impedance spectroscopy which is found to be the lowest (0.02 Ω cm{sup 2} at 800 °C) for cathode having highest degree of ‘A’-site deficiency. The same cathode composition exhibits a current density of 2.84 A cm{sup −2} (at 0.7 V, 800 °C) in anode-supported single cell. An attempt has been made to correlate the trend of electrical behaviour with increasing ‘A’-site deficiency for such cathode compositions.

  12. Variation in band gap of lanthanum chromate by transition metals doping LaCr{sub 0.9}A{sub 0.1}O{sub 3} (A:Fe/Co/Ni)

    SciTech Connect

    Naseem, Swaleha Khan, Wasi Saad, A. A. Shoeb, M. Ahmed, Hilal Naqvi, A. H.; Husain, Shahid

    2014-04-24

    Transition metal (Fe, Co, Ni) doped lanthanum chromate (LaCrO{sub 3}) nanoparticles (NPs) were prepared by gel combustion method and calcinated at 800°C. Microstructural studies were carried by XRD and SEM/EDS techniques. The results of structural characterization show the formation of all samples in single phase without any impurity. Optical properties were studied by UV- visible and photoluminescence techniques. The energy band gap was calculated and the variation was observed with the doping of transition metal ions. Photoluminescence spectra show the emission peak maxima for the pure LaCrO{sub 3} at about 315 nm. Influence of Fe, Co, Ni doping was studied and compared with pure lanthanum chromate nanoparticles.

  13. Formation mechanism and characteristics of lanthanum-doped BaTiO{sub 3} powders and ceramics prepared by the sol–gel process

    SciTech Connect

    Ianculescu, Adelina Carmen; Vasilescu, Catalina Andreea; Crisan, Maria; Raileanu, Malina; Vasile, Bogdan Stefan; Calugaru, Mihai; Crisan, Dorel; Dragan, Nicolae; Curecheriu, Lavinia; Mitoseriu, Liliana

    2015-08-15

    Pure and lanthanum-doped barium titanate nanopowders described by two different formulae, as Ba{sub 1−x}La{sub x}TiO{sub 3}, for lower La concentrations (0 ≤ x ≤ 0.005) and Ba{sub 1−x}La{sub x}Ti{sub 1−x/4}O{sub 3} for higher La concentration (x = 0.025) were prepared by an alkoxide sol–gel method. Single phase compositions were obtained after annealing at 900 °C for 2 h, in air. The increase of the lanthanum content causes structural and morphological changes in the oxide powders, including the evolution of the unit cell from tetragonal toward a cubic symmetry, the particle size decrease and a higher aggregation tendency. SEM investigations of the ceramics sintered at 1300 °C for 4 h indicate significant changes of the microstructural features (strong decrease of the average grain size and increase of the intergranular porosity) with the raise of La amount. Lanthanum addition to barium titanate prepared by sol–gel induces a more significant shift of the Curie temperature toward lower values, than that one reported in literature for ceramics of similar compositions, but processed by the conventional solid state method. The compositions with smaller La amount (x ≤ 0.005) show semiconducting properties at room temperature and high relative dielectric permittivity values, while the undoped ceramics and those doped with higher La content (x = 0.025) are good dielectrics. The ceramic with x = 0.025 exhibits acceptable low losses, a very diffuse ferroelectric–paraelectric transition and Curie temperature closed to the room temperature, being thus susceptible for high tunability applications. - Highlights: • Ba{sub 1−x}La{sub x}TiO{sub 3} (x ≤ 0.005) and Ba{sub 1−x}La{sub x}Ti{sub 1−x/4}O{sub 3} (x = 0.025) were prepared by sol–gel. • Ceramics with x < 0.5 exhibit semiconductor and high dielectric properties. • Ceramic with x = 0.025 exhibits acceptable low losses and diffuse phase transition.

  14. Study of the Durability of Doped Lanthanum Manganite and Cobaltite Cathode Materials under ''Real World'' Air Exposure Atmospheres

    SciTech Connect

    Singh, Prabhakar; Mahapatra, Manoj; Ramprasad, Rampi; Minh, Nguyen; Misture, Scott

    2014-11-30

    The overall objective of the program is to develop and validate mechanisms responsible for the overall structural and chemical degradation of lanthanum manganite as well as lanthanum ferrite cobaltite based cathode when exposed to “real world” air atmosphere exposure conditions during SOFC systems operation. Of particular interest are the evaluation and analysis of degradation phenomena related to and responsible for (a) products formation and interactions with air contaminants, (b) dopant segregation and oxide exolution at free surfaces, (c) cation interdiffusion and reaction products formation at the buried interfaces, (d) interface morphology changes, lattice transformation and the development of interfacial porosity and (e) micro-cracking and delamination from the stack repeat units. Reaction processes have been studied using electrochemical and high temperature materials compatibility tests followed by structural and chemical characterization. Degradation hypothesis has been proposed and validated through further experimentation and computational simulation.

  15. Design and fabrication of lanthanum-doped tin-silver-copper lead-free solder for the next generation of microelectronics applications in severe environment

    NASA Astrophysics Data System (ADS)

    Sadiq, Muhammad

    Tin-Lead solder (Sn-Pb) has long been used in the Electronics industry. But, due to its toxic nature and environmental effects, certain restrictions are made on its use by the European Rehabilitation of Hazardous Substances (RoHS) directive, and therefore, many researchers are looking to replace it. The urgent need for removing lead from solder alloys led to the very fast introduction of lead-free solder alloys without a deep knowledge of their behavior. Therefore, an extensive knowledge and understanding of the mechanical behavior of the emerging generation of lead-free solders is required to satisfy the demands of structural reliability. Sn-Ag-Cu (SAC) solders are widely used as lead-free replacements but their coarse microstructure and formation of hard and brittle Inter-Metallic Compounds (IMCs) have limited their use in high temperature applications. Many additives are studied to refine the microstructure and improve the mechanical properties of SAC solders including iron (Fe), bismuth (Bi), antimony (Sb) and indium (In) etc. Whereas many researchers studied the impact of novel rare earth (RE) elements like lanthanum (La), cerium (Ce) and lutetium (Lu) on SAC solders. These RE elements are known as “vitamins of metals” because of their special surface active properties. They reduce the surface free energy, refine the grain size and improve the mechanical properties of many lead free solder alloys like Sn-Ag, Sn-Cu and SAC but still a systematic study is required to explore the special effects of “La” on the eutectic SAC alloys. The objective of this PhD thesis is to extend the current knowledge about lead free solders of SAC alloys towards lanthanum doping with varying environmental conditions implemented during service. This thesis is divided into six main parts.

  16. Synthesis and Luminescence Properties of Novel Ce(3+)- and Eu(2+)-Doped Lanthanum Bromothiosilicate La3Br(SiS4)2 Phosphors for White LEDs.

    PubMed

    Lee, Szu-Ping; Liu, Shuang-De; Chan, Ting-Shan; Chen, Teng-Ming

    2016-04-13

    Novel Ce(3+)- and Eu(2+)-doped lanthanum bromothiosilicate La3Br(SiS4)2:Ce(3+)and La3Br(SiS4)2:Eu(2+) phosphors were prepared by solid-state reaction in an evacuated and sealed quartz glass ampule. The La3Br(SiS4)2:Ce(3+) phosphor generates a cyan emission upon excitation at 375 nm, whereas the La3Br(SiS4)2:Eu(2+) phosphor could be excited with extremely broad range from UV to blue region (300 to 600 nm) and generates a reddish-orange broadband emission centered at 640 nm. In addition, thermal luminescence properties of La3Br(SiS4)2:Ce(3+)and La3Br(SiS4)2:Eu(2+) phosphors from 20 to 200 °C were investigated. The combination of a 450 nm blue InGaN-based LED chip with the red-emitting La3Br(SiS4)2:Eu(2+) phosphor, and green-emitting BOSE:Eu(2+) commercial phosphor produced a warm-white light with the CRI value of ∼95 and the CCT of 5,120 K. Overall, these results show that the prepared phosphors may have potential applications in pc-WLED.

  17. Hydrothermal synthesis of doped lanthanum zirconate nanomaterials and the effect of V–Ge substitution on their structural, electrical and dielectric properties

    SciTech Connect

    Farid, Muhammad Asim; Asghar, Muhammad Adnan; Ashiq, Muhammad Naeem Ehsan, Muhammad Fahad; Athar, Muhammad

    2014-11-15

    Graphical abstract: Variation of dielectric constant with frequency for all the synthesized materials. - Highlights: • Hydrothermal method has been successfully employed to synthesize the zirconates. • XRD confirmed the formation of required phase. • Increased electrical resistivity makes these materials useful for microwave devices. • Dielectric parameters of zirconates decrease with increasing frequency. • Dielectric constant decreases with increasing substituents concentration. - Abstract: A hydrothermal method was successfully employed for the synthesis of a series of vanadium and germanium co-doped pyrochlore lanthanum zirconates with composition La{sub 2−x}V{sub x}Zr{sub 2−y}Ge{sub y}O{sub 7} (where x, y = 0.0, 0.25, 0.50, 0.75 and 1.0). The XRD and FTIR analyses confirmed the formation of single phase except vanadium and germanium substituted samples and the crystallite sizes are in the range of 7–31 nm for V{sup 3+}–Ge{sup 4+} substituted samples. The theoretical compositions are confirmed by the ED-XRF studies. The room temperature electrical resistivity increase with the substituents concentration which suggests that the synthesized materials can be used for microwave devices as such devices required highly resistive materials. Dielectric properties were measured in the frequency range of 6 kHz to 1 MHz. The dielectric parameters decrease with increase in frequency. The DC resistivity data is in good agreement with the dielectric data.

  18. Structural and magnetic properties of yttrium and lanthanum-doped Ni-Co and Ni-Co-Zn spinel ferrites

    SciTech Connect

    Stergiou, Charalampos; Litsardakis, George

    2014-11-05

    Rare earth doping of Co-rich spinel ferrites is investigated through the preparation of two groups of polycrystalline Ni-Co and Ni-Co-Zn ferrites, where Fe is partly substituted by Y and La. The characterization of the sintered ferrites by means of X-ray powder diffraction and Rietveld profile analysis, indicates the subtle expansion of the spinel unit cell and the cation redistribution in the doped ferrites in order to accommodate the incorporation of Y and La in the lattice. The impurity traces, detected only in the Ni-Co-Zn group, is ascribed to the Zn population in the tetrahedral A-sites impeding the cation transfer. Moreover, the examined microstructure of the doped Ni-Co samples comprises enlarged and more homogeneous grains, whereas grain growth is moderated in the doped Ni-Co-Zn ferrites. The discussed characteristics of the crystal and magnetic structure along with the morphological aspects define the impact of Y and La doping on the static magnetic properties of Ni-Co and Ni-Co-Zn ferrites, saturation magnetization MS and coercivity HC, which were extracted from the respective hysteresis loops.

  19. Tuning the Fermi-level of TiO2 mesoporous layer by lanthanum doping towards efficient perovskite solar cells.

    PubMed

    Gao, Xiao-Xin; Ge, Qian-Qing; Xue, Ding-Jiang; Ding, Jie; Ma, Jing-Yuan; Chen, Yao-Xuan; Zhang, Bao; Feng, Yaqing; Wan, Li-Jun; Hu, Jin-Song

    2016-09-29

    Tuning the band alignment is proved to be an effective way to facilitate carrier transportation and thus enhance the power conversion efficiency (PCE) of solar cells. Doping the compact layer with metal ions or modifying the interfaces among functional layers in perovskite solar cells (PSCs) can appreciably improve the PCE of PSCs. Inspired by the rare earth elemental doping of TiO2, which has witnessed the success in photocatalysis and dye-sensitized solar cells, we firstly demonstrated here that La(3+) doping in the mesoporous TiO2 layer of a mesostructured PSC can tune its Fermi level and thus significantly enhance the device PCE. Systematic analysis reveals that doping La(3+) into TiO2 raises the Fermi level of TiO2 through scavenging oxygen and inducing vacancies, which subsequently increases the open circuit voltage and the fill factor while reducing the series resistance of the PSC using La(3+)-doped TiO2 as a mesoporous layer. As a result, a PCE of 15.42% is achieved, which is appreciably higher than the PCE of a device with undoped TiO2 (12.11%).

  20. Photocatalytic degradation of Reactive Black 5 and Malachite Green with ZnO and lanthanum doped nanoparticles

    NASA Astrophysics Data System (ADS)

    Kaneva, N.; Bojinova, A.; Papazova, K.

    2016-02-01

    Here we report the preparation of ZnO particles with different concentrations of La3+ doping (0, 0.5 and 1 wt%) via sol-gel method. The nanoparticles are synthesized directly from Zn(CH3COO)2.2H2O in the presence of 1-propanol and triethylamine at 80°C. The conditions are optimized to obtain particles of uniform size, easy to isolate and purify. The nanoparticles are characterized by SEM, XRD and UV-Vis analysis. The photocatalytic properties of pure and La-doped ZnO are studied in the photobleaching of Malachite Green (MG) and Reactive Black 5 (RB5) dyes in aqueous solutions upon UV illumination. It is observed that the rate constant increases with the La loading up to 1 wt%. The doping helps to achieve complete mineralization of MG within a short irradiation time. 1 wt% La-doped ZnO nanoparticles show highest photocatalytic activity. The La3+ doped ZnO particles degrade faster RB5 than MG. The reason is weaker N=N bond in comparison with the C-C bond between the central carbon atom and N,N-dimethylaminobenzyl in MG. The as-prepared ZnO particles can find practical application in photocatalytic purification of textile wastewaters.

  1. Spin injection and detection in lanthanum- and niobium-doped SrTiO3 using the Hanle technique.

    PubMed

    Han, Wei; Jiang, Xin; Kajdos, Adam; Yang, See-Hun; Stemmer, Susanne; Parkin, Stuart S P

    2013-01-01

    There has been much interest in the injection and detection of spin-polarized carriers in semiconductors for the purposes of developing novel spintronic devices. Here we report the electrical injection and detection of spin-polarized carriers into Nb-doped strontium titanate single crystals and La-doped strontium titanate epitaxial thin films using MgO tunnel barriers and the three-terminal Hanle technique. Spin lifetimes of up to ~100 ps are measured at room temperature and vary little as the temperature is decreased to low temperatures. However, the mobility of the strontium titanate has a strong temperature dependence. This behaviour and the carrier doping dependence of the spin lifetime suggest that the spin lifetime is limited by spin-dependent scattering at the MgO/strontium titanate interfaces, perhaps related to the formation of doping induced Ti(3+). Our results reveal a severe limitation of the three-terminal Hanle technique for measuring spin lifetimes within the interior of the subject material.

  2. Development of Lanthanum Ferrite SOFC Cathodes

    SciTech Connect

    Simner, Steve P.; Bonnett, Jeff F.; Canfield, Nathan L.; Meinhardt, Kerry D.; Shelton, Jayne P.; Sprenkle, Vince L.; Stevenson, Jeffry W.

    2003-01-01

    A number of studies have been conducted concerning compositional/microstructural modifications of a Sr-doped lanthanum ferrite (LSF) cathode and protective Sm-doped ceria (SDC) layer in an anode supported solid oxide fuel cell (SOFC). Emphasis was placed on achieving enhanced low temperature (700-800 degrees C) performance, and long-term cell stability. Investigations involved manipulation of the lanthanum ferrite chemistry, addition of noble metal oxygen reduction catalysts, incorporation of active cathode layer compositions containing Co, Fe and higher Sr contents, and attempts to optimize the ceria barrier layer between the LSF cathode and YSZ electrolyte.

  3. Fabrication of lanthanum-doped thorium dioxide by high-energy ball milling and spark plasma sintering

    NASA Astrophysics Data System (ADS)

    Scott, Spencer M.; Yao, Tiankai; Lu, Fengyuan; Xin, Guoqing; Zhu, Weiguang; Lian, Jie

    2017-03-01

    High-energy ball milling was used to synthesize Th1-xLaxO2-0.5x (x = 0.09, 0.23) solid solutions, as well as improve the sinterability of ThO2 powders. Dense La-doped ThO2 pellets with theoretical density above 94% were consolidated by spark plasma sintering at temperatures above 1400 °C for 20 min, and the densification behavior and the non-equilibrium effects on phase and structure were investigated. A lattice contraction of the SPS-densified pellets occurred with increasing ball milling duration, and a secondary phase with increased La-content was observed in La-doped pellets. A dependence on the La-content and sintering duration for the onset of localized phase segregation has been proposed. The effects of high-energy ball milling, La-content, and phase formation on the thermal diffusivity were also studied for La-doped ThO2 pellets by laser flash measurement. Increasing La-content and high energy ball milling time decreases thermal diffusivity; while the sintering peak temperature and holding time beyond 1600 °C dramatically altered the temperature dependence of the thermal diffusivity beyond 600 °C.

  4. Magnetic phase transition and clustered state in Ca-doped lanthanum cobaltite and manganite with insulator ground states.

    PubMed

    Ryzhov, V A; Lazuta, A V; Khavronin, V P; Molkanov, P L; Mukovskii, Ya M

    2014-02-19

    The transport and magnetic properties (ac linear and nonlinear (second and third orders) susceptibilities) are presented for La0.8Ca0.2MnO3 and La0.8Ca0.2CoO3 single crystals with insulator ground states. The ferromagnetic (FM) clusters with similar magnetic characteristics originate in the paramagnetic phases of both compounds below some temperature T(∗). At high temperatures the FM clusters arise at the preferable sites that can be attributed to the chemical inhomogeneities, their density being weakly T-dependent. On cooling a homogeneous nucleation of the FM clusters develops below a definite temperature T(#) that is characterized by a fast growth of their density. These two stages are observed in both compounds. At the third stage a coalescence of the FM clusters starts in the doped cobaltite, whereas in the manganite the development of matrix FM ordering occurs which changes a cluster's behavior. The indicated features support the common nature of the cluster state in the doped cobaltite and manganite. The difference in their evolution is a consequence of the different magnetic properties of the matrices in the manganite and cobaltite.

  5. Novel Au/La-SrTiO3 microspheres: superimposed effect of gold nanoparticles and lanthanum doping in photocatalysis.

    PubMed

    Wang, Guannan; Wang, Pei; Luo, He-Kuan; Hor, T S Andy

    2014-07-01

    Novel multielement Au/La-SrTiO(3) microspheres were synthesized by a solvothermal method using monodisperse gold and La-SrTiO(3) nanocrystals as building blocks. The porous Au/La-SrTiO(3) microspheres had a large surface area of 94.6 m(2)  g(-1). The stable confined Au nanoparticles demonstrated strong surface plasmon resonance effect, leading to enhanced absorption in a broad UV/Vis/NIR range. Doping of rare-earth metal La also broadened the absorption band to the visible region. Both the conduction and valence bands of Au/La-SrTiO(3) microspheres thus show favorable potential for proton reduction under visible light. The superimposed effect of Au nanoparticles and La doping in Au/La-SrTiO(3) microspheres led to high photocurrent density in photoelectrochemical water splitting and good photocatalytic activity in photodegradation of rhodamine B. The photocatalytic activities are in the order of the following: Au/La-SrTiO(3) microspheres>Au/SrTiO(3) microspheres>La-SrTiO(3) microspheres>SrTiO(3) microspheres.

  6. Built-in Electric Field Induced Mechanical Property Change at the Lanthanum Nickelate/Nb-doped Strontium Titanate Interfaces

    NASA Astrophysics Data System (ADS)

    Chien, Teyu; Liu, Jian; Yost, Andrew J.; Chakhalian, Jak; Freeland, John W.; Guisinger, Nathan P.

    2016-01-01

    The interactions between electric field and the mechanical properties of materials are important for the applications of microelectromechanical and nanoelectromechanical systems, but relatively unexplored for nanoscale materials. Here, we observe an apparent correlation between the change of the fractured topography of Nb-doped SrTiO3 (Nb:STO) within the presence of a built-in electric field resulting from the Schottky contact at the interface of a metallic LaNiO3 thin film utilizing cross-sectional scanning tunneling microscopy and spectroscopy. The change of the inter-atomic bond length mechanism is argued to be the most plausible origin. This picture is supported by the strong-electric-field-dependent permittivity in STO and the existence of the dielectric dead layer at the interfaces of STO with metallic films. These results provided direct evidence and a possible mechanism for the interplay between the electric field and the mechanical properties on the nanoscale for perovskite materials.

  7. Built-in Electric Field Induced Mechanical Property Change at the Lanthanum Nickelate/Nb-doped Strontium Titanate Interfaces.

    PubMed

    Chien, TeYu; Liu, Jian; Yost, Andrew J; Chakhalian, Jak; Freeland, John W; Guisinger, Nathan P

    2016-01-08

    The interactions between electric field and the mechanical properties of materials are important for the applications of microelectromechanical and nanoelectromechanical systems, but relatively unexplored for nanoscale materials. Here, we observe an apparent correlation between the change of the fractured topography of Nb-doped SrTiO3 (Nb:STO) within the presence of a built-in electric field resulting from the Schottky contact at the interface of a metallic LaNiO3 thin film utilizing cross-sectional scanning tunneling microscopy and spectroscopy. The change of the inter-atomic bond length mechanism is argued to be the most plausible origin. This picture is supported by the strong-electric-field-dependent permittivity in STO and the existence of the dielectric dead layer at the interfaces of STO with metallic films. These results provided direct evidence and a possible mechanism for the interplay between the electric field and the mechanical properties on the nanoscale for perovskite materials.

  8. Built-in Electric Field Induced Mechanical Property Change at the Lanthanum Nickelate/Nb-doped Strontium Titanate Interfaces

    PubMed Central

    Chien, TeYu; Liu, Jian; Yost, Andrew J.; Chakhalian, Jak; Freeland, John W.; Guisinger, Nathan P.

    2016-01-01

    The interactions between electric field and the mechanical properties of materials are important for the applications of microelectromechanical and nanoelectromechanical systems, but relatively unexplored for nanoscale materials. Here, we observe an apparent correlation between the change of the fractured topography of Nb-doped SrTiO3 (Nb:STO) within the presence of a built-in electric field resulting from the Schottky contact at the interface of a metallic LaNiO3 thin film utilizing cross-sectional scanning tunneling microscopy and spectroscopy. The change of the inter-atomic bond length mechanism is argued to be the most plausible origin. This picture is supported by the strong-electric-field-dependent permittivity in STO and the existence of the dielectric dead layer at the interfaces of STO with metallic films. These results provided direct evidence and a possible mechanism for the interplay between the electric field and the mechanical properties on the nanoscale for perovskite materials. PMID:26743875

  9. Built-in Electric Field Induced Mechanical Property Change at the Lanthanum Nickelate/Nb-doped Strontium Titanate Interfaces

    DOE PAGES

    Chien, TeYu; Liu, Jian; Yost, Andrew J.; ...

    2016-01-08

    The interactions between electric field and the mechanical properties of materials are important for the applications of microelectromechanical and nanoelectromechanical systems, but relatively unexplored for nanoscale materials. Here, we observe an apparent correlation between the change of the fractured topography of Nb-doped SrTiO3 (Nb:STO) within the presence of a built-in electric field resulting from the Schottky contact at the interface of a metallic LaNiO3 thin film utilizing cross-sectional scanning tunneling microscopy and spectroscopy. The change of the inter-atomic bond length mechanism is argued to be the most plausible origin. This picture is supported by the strong-electric-field-dependent permittivity in STO andmore » the existence of the dielectric dead layer at the interfaces of STO with metallic films. Finally, these results provided direct evidence and a possible mechanism for the interplay between the electric field and the mechanical properties on the nanoscale for perovskite materials.« less

  10. Built-in Electric Field Induced Mechanical Property Change at the Lanthanum Nickelate/Nb-doped Strontium Titanate Interfaces

    SciTech Connect

    Chien, TeYu; Liu, Jian; Yost, Andrew J.; Chakhalian, Jak; Freeland, John W.; Guisinger, Nathan P.

    2016-01-08

    The interactions between electric field and the mechanical properties of materials are important for the applications of microelectromechanical and nanoelectromechanical systems, but relatively unexplored for nanoscale materials. Here, we observe an apparent correlation between the change of the fractured topography of Nb-doped SrTiO3 (Nb:STO) within the presence of a built-in electric field resulting from the Schottky contact at the interface of a metallic LaNiO3 thin film utilizing cross-sectional scanning tunneling microscopy and spectroscopy. The change of the inter-atomic bond length mechanism is argued to be the most plausible origin. This picture is supported by the strong-electric-field-dependent permittivity in STO and the existence of the dielectric dead layer at the interfaces of STO with metallic films. Finally, these results provided direct evidence and a possible mechanism for the interplay between the electric field and the mechanical properties on the nanoscale for perovskite materials.

  11. Effect of sintering time on structural, microstructural and chemical composition of Ni-doped lanthanum gallate perovskites

    SciTech Connect

    Colomer, M.T.

    2015-08-15

    This work reports the effect of two different sintering times, 6 and 48 h on the structural, microstructural, and chemical features of Ni-doped La{sub 0.90}Sr{sub 0.10}GaO{sub 3.00−δ}. Independently of the sintering time, La{sub 0.90}Sr{sub 0.10}Ga{sub 1−x}Ni{sub x}O{sub 3.00−δ} (where x=0.10, and 0.20 (mol)) presents a rhombohedral symmetry with a lattice volume that decreases when NiO dopant increases. Besides the perovskite, LaSrGa{sub 3.00}O{sub 7.00} (nominal composition) is present as second phase in all cases. When the samples are doped with NiO, the peaks of this second phase are shifted with respect to the peaks of the pure phase. These shifts suggest that this second phase could admit some Ni ions in its structure. According to the XRD patterns, the amount of the latter phase is larger when sintering time is increased. Electron probe microanalysis (EPMA) indicated that the matrix of the samples sintered for 6 h is constituted by a perovskite with an experimental composition very close to the nominal one. However, when the samples are sintered for 48 h the matrix of each sample is constituted by two perovskites; both with compositional deviations with respect to their nominal one. In particular, a significant Sr depletion compensated by a La increment in the A site is observed. Those compositional deviations could be mainly due to the diffusion of the cations in the bulk and/or from the bulk to the surface of the samples. That diffusion can favour the formation, not only, of a second perovskite with a different composition in relation with the first one formed, but also, the formation of second phases. In addition, a very slight broadening of Bragg peaks of the perovskites sintered for 48 h is observed by XRD and can be related to the presence of two different perovskites in each sample according to EPMA results. By BSEM and EPMA analyses La{sub 4.00}Ga{sub 2.00}O{sub 9.00} (nominal composition) is also observed as second phase when samples are

  12. Defect equilibria and chemical expansion in undoped and doped ceria and strontium doped lanthanum cobalt iron oxide oxygen conducting materials and their applications in solid-state electrochemical cells

    NASA Astrophysics Data System (ADS)

    Bishop, Sean R.

    Ceramic oxygen conducting materials are used in many energy-related applications from fuel reforming to electricity generation. In a typical ceramic oxygen conductor, oxygen ions are transmitted through a dense membrane via defects in the material. Hence, defects control the performance of these materials. In low oxygen partial pressure, ceria based materials become non-stoichiometric and can form defect complexes that hinder ionic conductivity. In addition, oxygen non-stoichiometry induces strain (chemical expansion) that can result in stresses for composite or constrained applications. In this dissertation the non-stoichiometry and chemical expansion behavior is reported as a function of PO2 for undoped ceria, gadolinium doped ceria (GDC) and strontium doped lanthanum cobalt iron oxide (LSCF). Undoped ceria was measured at 800°C and GDC and LSCF at 600--900°C in a wide PO2 range. It was found that defect interactions could effectively be modeled in ceria based materials using defect complex formation in a mass action formalism and the results were used to model nonlinear chemical expansion behavior. In LSCF, non-stoichiometry and chemical expansion were modeled using using metallic and semi-conductor models. A semi-conductor model with B-site small polarons best represented the measured behavior. The resulting models and parameters can be used to predict mechanical and electrical behavior of SOFC components. Surface oxygen non-stoichiometry has also been measured by comparing low surface area to high surface area samples. It was found that surface defect concentration previously ignored in the literature can result in erroneous non-stoichiometry measurements. In the latter half of this dissertation these materials are applied in SOFC and ceramic oxygen generator (COG) technology. A strategy is presented here for advanced life support systems employs a catalytic layer combined with a COG cell so that CO2 is reduced all the way to solid carbon and oxygen without

  13. Crystal structure and ionic conductivity of Mg-doped apatite-type lanthanum silicates La10Si6-xMgxO27-x (x = 0-0.4)

    NASA Astrophysics Data System (ADS)

    Yin, Guang-Chao; Yin, Hong; Zhong, Lin-Hong; Sun, Mei-Ling; Zhang, Jun-Kai; Xie, Xiao-Jun; Cong, Ri-Dong; Wang, Xin; Gao, Wei; Cui, Qi-Liang

    2014-04-01

    Lanthanum silicates La10Si6-xMgxO27-x (x = 0-0.4) were prepared by solid state synthesis to investigate the effect of Mg doping on crystal structure and ionic conductivity. Rietveld analysis of the powder XRD patterns reveals that Mg substitution on Si site results in significant enlargement of channel triangles, favoring oxide-ion conduction. Furthermore, an increase of Mg concentration significantly influences the linear density of interstitial oxygen, which plays an important role in ionic conductivity. The Arrhenius plots of La10Si6-xMgxO27-x (x = 0-0.4) suggest that Mg-doped samples present higher conductivity and lower activation energy than non-doped La10Si6O27, and La10Si5.8Mg0.2O26.8 exhibits the highest conductivity with a value of 3.0×10-2 S ·cm-1 at 700 °C. Such conductive behavior agrees well with the refined results. The corresponding mechanism has been discussed in this paper.

  14. Nitride tuning of lanthanide chromites.

    PubMed

    Black, Ashley P; Johnston, Hannah E; Oró-Solé, Judith; Bozzo, Bernat; Ritter, Clemens; Frontera, Carlos; Attfield, J Paul; Fuertes, Amparo

    2016-03-21

    LnCrO(3-x)N(x) perovskites with Ln = La, Pr and Nd and nitrogen contents up to x = 0.59 have been synthesised through ammonolysis of LnCrO4 precursors. These new materials represent one of the few examples of chromium oxynitrides. Hole-doping through O(2-)/N(3-) anion substitution suppresses the magnetic transition far less drastically than Ln(3+)/M(2+) (M = Ca, Sr) cation substitutions because of the greater covalency of metal-nitride bonds. Hence, nitride-doping is a more benign method for doping metal oxides without suppressing electronic transitions.

  15. Chromite alteration processes within Vourinos ophiolite

    NASA Astrophysics Data System (ADS)

    Grieco, Giovanni; Merlini, Anna

    2012-09-01

    The renewed interest in chromite ore deposits is directly related to the increase in Cr price ruled by international market trends. Chromite, an accessory mineral in peridotites, is considered to be a petrogenetic indicator because its composition reflects the degree of partial melting that the mantle experienced while producing the chromium spinel-bearing rock (Burkhard in Geochim Cosmochim Acta 57:1297-1306, 1993). However, the understanding of chromite alteration and metamorphic modification is still controversial (e.g. Evans and Frost in Geochim Cosmochim Acta 39:959-972, 1975; Burkhard in Geochim Cosmochim Acta 57:1297-1306, 1993; Oze et al. in Am J Sci 304:67-101, 2004). Metamorphic alteration leads to major changes in chromite chemistry and to the growth of secondary phases such as ferritchromite and chlorite. In this study, we investigate the Vourinos complex chromitites (from the mines of Rizo, Aetoraches, Xerolivado and Potamia) with respect to textural and chemical analyses in order to highlight the most important trend of alteration related to chromite transformation. The present study has been partially funded by the Aliakmon project in collaboration between the Public Power Corporation of Greece and Institute of Geology and Mineral Exploration of Kozani.

  16. Periclase-chromite refractories from fused materials

    SciTech Connect

    Slovikovskii, V.V.; Eroshkina, V.I.; Kononenko, G.V.; Nechistykh, G.A.; Simonov, K.V.

    1985-11-01

    Experiments were carried out to obtain high-grade fused chromitepericlase. It is shown that during the melting of batch consisting of raw magnesite and chromite ore the process of reducing the chromite ore to metallic ferrochromium is eliminated, which adversely affects both the content of Cr/sub 2/O/sub 3/ in the fused material, and also the commercial appearance of the resulting refractories. The authors developed a technology for preparing periclase-chromite refractories with chrommite-periclase constituents. The goods obtained possess good physicoceramic properties and a low content of silicites. The articles thus prepared were used to make the linings of the most critical parts of the converters which allowed an increase to be made in the duration of campaigns for the Kivset units of 1.5-2 times.

  17. Tunable quasi-cw two-micron lasing in diode-pumped crystals of mixed Tm{sup 3+}-doped sodium - lanthanum - gadolinium molybdates and tungstates

    SciTech Connect

    Bol'shchikov, F A; Ryabochkina, P A; Zharikov, Evgeny V; Lis, Denis A; Subbotin, Kirill A; Zakharov, N G; Antipov, Oleg L

    2010-12-09

    Two-micron lasing is obtained for the first time on the {sup 3}F{sub 4} {yields} {sup 3}H{sub 6} transition of Tm{sup 3+} ions in diode-pumped crystals of mixed sodium - lanthanum - gadolinium tungstate Tm:NaLa{sub 1/2}Gd{sub 1/2}(WO{sub 4}){sub 2} (C{sub Tm} = 3.6 at %) (3.6Tm : NLGW) and molybdate Tm:NaLa{sub 1/3}Gd{sub 2/3}(MoO{sub 4}){sub 2} (C{sub Tm} = 4.8 at %) (4.8Tm : NLGM). For the 3.6Tm : NLGW crystal, the quasi-cw laser output power exceeded 200 mW and the slope efficiency (with respect to absorbed pump power) for the {pi}- and {sigma}-polarisations at wavelengths of 1908 and 1918 nm was 34% and 30%, respectively. The laser wavelength of this crystal was continuously tuned within the spectral range of 1860 - 1935 nm. For the 4.8Tm : NLGM crystal, the slope efficiency for the {pi}- and {sigma}-polarisations at wavelengths of 1910 and 1918 nm was 27% and 23%, respectively, and the laser wavelength was tunable within the spectral range of 1870 - 1950 nm. (lasers)

  18. Podiform chromite deposits--database and grade and tonnage models

    USGS Publications Warehouse

    Mosier, Dan L.; Singer, Donald A.; Moring, Barry C.; Galloway, John P.

    2012-01-01

    Chromite ((Mg, Fe++)(Cr, Al, Fe+++)2O4) is the only source for the metallic element chromium, which is used in the metallurgical, chemical, and refractory industries. Podiform chromite deposits are small magmatic chromite bodies formed in the ultramafic section of an ophiolite complex in the oceanic crust. These deposits have been found in midoceanic ridge, off-ridge, and suprasubduction tectonic settings. Most podiform chromite deposits are found in dunite or peridotite near the contact of the cumulate and tectonite zones in ophiolites. We have identified 1,124 individual podiform chromite deposits, based on a 100-meter spatial rule, and have compiled them in a database. Of these, 619 deposits have been used to create three new grade and tonnage models for podiform chromite deposits. The major podiform chromite model has a median tonnage of 11,000 metric tons and a mean grade of 45 percent Cr2O3. The minor podiform chromite model has a median tonnage of 100 metric tons and a mean grade of 43 percent Cr2O3. The banded podiform chromite model has a median tonnage of 650 metric tons and a mean grade of 42 percent Cr2O3. Observed frequency distributions are also given for grades of rhodium, iridium, ruthenium, palladium, and platinum. In resource assessment applications, both major and minor podiform chromite models may be used for any ophiolite complex regardless of its tectonic setting or ophiolite zone. Expected sizes of undiscovered podiform chromite deposits, with respect to degree of deformation or ore-forming process, may determine which model is appropriate. The banded podiform chromite model may be applicable for ophiolites in both suprasubduction and midoceanic ridge settings.

  19. Pneumoconiosis in Chromite Miners in South Africa1

    PubMed Central

    Sluis-Cremer, G. K.; Du Toit, R. S. J.

    1968-01-01

    Ten chromite miners in South Africa have been found to show radiological evidence of a fine nodulation; five of these miners had worked only in chromite mines. These cases occurred in a labour force of some 1,500 persons subjected to regular examination. Clinical evidence and the results of intratracheal injection of chromite suspension into rats indicate that the radiological changes are due not to fibrosis but to a benign deposition of chromite (Cr2O3FeO) dust in the lungs. Images PMID:5642648

  20. Chromite from the Blue Ridge province of North Carolina.

    USGS Publications Warehouse

    Lipin, B.R.

    1984-01-01

    Chromite is found as ubiquitous accessory grains and occasional segregations within dunite bodies. Results of analysis of chromite textures and chemistry and estimation of equilibration T of olivine-chromite pairs are cited as evidence that the dunites are metamorphic rocks rather than primary mantle peridotites. They are considered to be disrupted fragments of ophiolites that were emplaced before or during the peak of Ordovician metamorphism which was responsible for dehydration of serpentine-bearing rocks and alteration of chromite compositions and textures.-M.S.

  1. Lanthanum fluoride nanoparticles for radiosensitization of tumors

    NASA Astrophysics Data System (ADS)

    Kudinov, Konstantin; Bekah, Devesh; Cooper, Daniel; Shastry, Sathvik; Hill, Colin; Bradforth, Stephen; Nadeau, Jay

    2016-03-01

    Dense inorganic nanoparticles have recently been identified as promising radiosensitizers. In addition to dose enhancement through increased attenuation of ionizing radiation relative to biological tissue, scintillating nanoparticles can transfer energy to coupled photosensitizers to amplify production of reactive oxygen species, as well as provide UVvisible emission for optical imaging. Lanthanum fluoride is a transparent material that is easily prepared as nanocrystals, and which can provide radioluminescence at a number of wavelengths through simple substitution of lanthanum ions with other luminescent lanthanides. We have prepared lanthanum fluoride nanoparticles doped with cerium, terbium, or both, that have good spectral overlap with chlorine6 or Rose Bengal photosensitizer molecules. We have also developed a strategy for stable conjugation of the photosensitizers to the nanoparticle surface, allowing for high energy transfer efficiencies on a per molecule basis. Additionally, we have succeeded in making our conjugates colloidally stable under physiological conditions. Here we present our latest results, using nanoparticles and nanoparticle-photosensitizer conjugates to demonstrate radiation dose enhancement in B16 melanoma cells. The effects of nanoparticle treatment prior to 250 kVp x-ray irradiation were investigated through clonogenic survival assays and cell cycle analysis. Using a custom apparatus, we have also observed scintillation of the nanoparticles and conjugates under the same conditions that the cell samples are irradiated.

  2. Effect of trace lanthanum ion on dissolution and crystal growth of calcium carbonate

    NASA Astrophysics Data System (ADS)

    Kamiya, Natsumi; Kagi, Hiroyuki; Tsunomori, Fumiaki; Tsuno, Hiroshi; Notsu, Kenji

    2004-07-01

    Impurity effects of trace lanthanum ion (La 3+) on the dissolution and growth of calcium carbonate were studied with in situ observation techniques. Dissolution kinetics of two polymorphs of calcium carbonate, calcite and vaterite, were investigated by monitoring the pH in the solution with laser-induced fluorescence spectroscopy using a pH-sensitive reagent, seminaphthorhodafluors. No effect on dissolution of vaterite was observed with the spectroscopic observations, whereas calcite dissolution was significantly inhibited by lanthanum ion with concentrations higher than 1 μM. Crystal growth and dissolution processes of calcite under the lanthanum-doped condition were observed by means of atomic force microscopy. Step propagations during crystal growth and dissolution of calcite were inhibited by trace lanthanum ion (5 μM). An insoluble thin layer of lanthanum carbonate deposited on the step site of the calcite surface could be a possible cause of the inhibitions observed both for dissolution and growth.

  3. Preparation of Ho3+/Tm3+ Co-doped Lanthanum Tungsten Germanium Tellurite Glass Fiber and Its Laser Performance for 2.0 μm

    NASA Astrophysics Data System (ADS)

    Zhou, Dechun; Bai, Xuemei; Zhou, Hang

    2017-03-01

    Ho3+/Tm3+ co-doped 50TeO2-25GeO2-3WO3-5La2O3-3Nb2O5-5Li2O-9BaF2 glass fiber is prepared with the rod-tube drawing method of 15 μm core diameter and 125 μm inner cladding diameter applied in the 2.0 μm-infrared laser. The 2.0 μm luminescence properties of the core glass are researched and the fluorescence intensity variation for different Tm3+ doping concentration is systematically analyzed. The results show that the 2.0 μm luminescence of Ho3+ is greatly influenced by the doping concentration ratio of Ho3+ to Tm3+ and that the maximum fluorescence intensity of the core glass can be obtained and its emission cross section can reach 0.933 × 10‑21 cm2 when the sensitized proportion of holmium to thulium is 0.3 to 0.7 (mol%). Simultaneously, the maximum phonon energy of the core glass sample is 753 cm‑1, which is significantly lower than that of silicate, gallate and germanate glass and the smaller matrix phonon energy can be conductive to the increase 2.0 μm-band emission intensity. The continuous laser with the maximum laser output power of 0.993 W and 2051 nm -wavelength of 31.9%-slope efficiency is output within the 0.5 m glass fiber and the experiment adopts 1560 nm erbium-doped fiber laser(EDFL) as the pump source and the self-built all-fiber laser. Therefore, the glass fiber has excellent laser characteristics and it is suitable for the 2.0 μm-band laser.

  4. Preparation of Ho(3+)/Tm(3+) Co-doped Lanthanum Tungsten Germanium Tellurite Glass Fiber and Its Laser Performance for 2.0 μm.

    PubMed

    Zhou, Dechun; Bai, Xuemei; Zhou, Hang

    2017-03-17

    Ho(3+)/Tm(3+) co-doped 50TeO2-25GeO2-3WO3-5La2O3-3Nb2O5-5Li2O-9BaF2 glass fiber is prepared with the rod-tube drawing method of 15 μm core diameter and 125 μm inner cladding diameter applied in the 2.0 μm-infrared laser. The 2.0 μm luminescence properties of the core glass are researched and the fluorescence intensity variation for different Tm(3+) doping concentration is systematically analyzed. The results show that the 2.0 μm luminescence of Ho(3+) is greatly influenced by the doping concentration ratio of Ho(3+) to Tm(3+) and that the maximum fluorescence intensity of the core glass can be obtained and its emission cross section can reach 0.933 × 10(-21) cm(2) when the sensitized proportion of holmium to thulium is 0.3 to 0.7 (mol%). Simultaneously, the maximum phonon energy of the core glass sample is 753 cm(-1), which is significantly lower than that of silicate, gallate and germanate glass and the smaller matrix phonon energy can be conductive to the increase 2.0 μm-band emission intensity. The continuous laser with the maximum laser output power of 0.993 W and 2051 nm -wavelength of 31.9%-slope efficiency is output within the 0.5 m glass fiber and the experiment adopts 1560 nm erbium-doped fiber laser(EDFL) as the pump source and the self-built all-fiber laser. Therefore, the glass fiber has excellent laser characteristics and it is suitable for the 2.0 μm-band laser.

  5. Preparation of Ho3+/Tm3+ Co-doped Lanthanum Tungsten Germanium Tellurite Glass Fiber and Its Laser Performance for 2.0 μm

    PubMed Central

    Zhou, Dechun; Bai, Xuemei; Zhou, Hang

    2017-01-01

    Ho3+/Tm3+ co-doped 50TeO2-25GeO2-3WO3-5La2O3-3Nb2O5-5Li2O-9BaF2 glass fiber is prepared with the rod-tube drawing method of 15 μm core diameter and 125 μm inner cladding diameter applied in the 2.0 μm-infrared laser. The 2.0 μm luminescence properties of the core glass are researched and the fluorescence intensity variation for different Tm3+ doping concentration is systematically analyzed. The results show that the 2.0 μm luminescence of Ho3+ is greatly influenced by the doping concentration ratio of Ho3+ to Tm3+ and that the maximum fluorescence intensity of the core glass can be obtained and its emission cross section can reach 0.933 × 10−21 cm2 when the sensitized proportion of holmium to thulium is 0.3 to 0.7 (mol%). Simultaneously, the maximum phonon energy of the core glass sample is 753 cm−1, which is significantly lower than that of silicate, gallate and germanate glass and the smaller matrix phonon energy can be conductive to the increase 2.0 μm-band emission intensity. The continuous laser with the maximum laser output power of 0.993 W and 2051 nm -wavelength of 31.9%-slope efficiency is output within the 0.5 m glass fiber and the experiment adopts 1560 nm erbium-doped fiber laser(EDFL) as the pump source and the self-built all-fiber laser. Therefore, the glass fiber has excellent laser characteristics and it is suitable for the 2.0 μm-band laser. PMID:28303946

  6. PGM in chromite ore of the Sopcheozero deposit, Kola Peninsula

    NASA Astrophysics Data System (ADS)

    Neradovsky, Yu. N.; Savchenko, E. E.

    2008-12-01

    The Sopcheozero chromite deposit is hosted in dunite of the Monchegorsk layered intrusion as a sheetlike body of disseminated ore with a chromite grade varying from 20 to 60%. The total PGM content in the ore attains 0.5-0.8 g/t. The composition of host rocks varies from plagioclase peridotite to dunite, but PGM were found only in chromite-bearing dunite. PGM inclusions were detected in the interstices of chromite and olivine grains and within grains themselves. The data obtained confirm the known tendency toward variation in PGM composition with increasing sulfur and light PGE contents in the residual magmatic melt. The first particles of refractory Ir, Os, and Ru intermetallides appeared at the final stage of olivine crystallization, whereas laurite (Ru,Os,Ir)S2 and pentlandite (Fe,Ni)9S8 were formed at the final stage of chromite crystallization, when the sulfur concentration in the residual melt became sufficient.

  7. ZIRCONIA-BASED MIXED POTENTIAL CARBON MONOXIDE/HYDROCARBON SENSORS WITH LANTHANUM MAGNESIUM OXIDE, AND TERBIUM-DOPED YTTRIUM STABILIZED ZIRCONIA ELECTRODES

    SciTech Connect

    E. L. BROSHA; R. MUKUNDAN; ET AL

    2000-10-01

    We have investigated the performance of dual metal oxide electrode mixed potential sensors in an engine-out, dynamometer environment. Sensors were fabricated by sputtering thin films of LaMnO{sub 3} and Tb-doped YSZ onto YSZ electrolyte. Au gauze held onto the metal oxide thin films with Au ink was used for current collection. The exhaust gas from a 4.8L, V8 engine operated in open loop, steady-state mode around stoichiometry at 1500 RPM and 50 Nm. The sensor showed a stable EMF response (with no hysteresis) to varying concentrations of total exhaust gas HC content. The sensor response was measured at 620 and 670 C and shows temperature behavior characteristic of mixed potential-type sensors. The results of these engine-dynamometer tests are encouraging; however, the limitations associated with Au current collection present the biggest impediment to automotive use.

  8. Low-temperature magnetism of troilite and chromite

    NASA Astrophysics Data System (ADS)

    Kohout, T.; Cuda, J.; Tucek, J.; Haloda, J.; Filip, J.; Zboril, R.

    2011-12-01

    Troilite is the stoichiometric end-member of the pyrrhotite mineral group and ranks among the most wide-spread minerals in extraterrestrial materials. The low temperature magnetic data measured on troilite powderized fraction extracted from the Bruderheim L6 chondrite and Cape York IIIA iron meteorites suggest an existence of the magnetic transition at ≈ 70 K (Kohout et al. 2007, 2010). However, Gattacceca et al., 2011 recently suggested that this magnetic transition is not intrinsic to troilite but is rather a signature of Curie temperature of chromite present as secondary phase in troilite samples. Chromite is another important phase present in extraterrestrial materials and for certain composition can have its Curie temperature in this temperature range. Thus, we reviewed our data and conducted additional measurements to distinguish a nature of this phenomena. The new results indicate: ? The evolution of induced magnetization during heating through the transition does not follow (even roughly) Curie-Weiss law and thus does not resemble transition from ferrimagnetic into paramagnetic state as expected for chromite. ? The transition in troilite samples reveals itself on room temperature saturation isothermal remanence cooling and heating curves (RT-SIRM cycle) what is in contrary to data and interpretation provided by Gattacceca et al., 2011 for chromite case. ? The purity of our samples was studied using electron microprobe analysis and backscattered electron observations on polished troilite grains and no evidence of chromite was observed down to submicron scale. ? No presence of chromite was observed in x-ray diffraction nor in Mössbauer spectra. In order to explain the observed magnetic transition to be caused by chromite contamination, roughly 4% of chromite are required to be present within troilite (Gattacceca et al. 2011). Our observations summarized above does not reveal presence of chromite (detection limit ~1%) and indicate rather different magnetic

  9. Encephalopathy caused by lanthanum carbonate.

    PubMed

    Fraile, Pilar; Cacharro, Luis Maria; Garcia-Cosmes, Pedro; Rosado, Consolacion; Tabernero, Jose Matias

    2011-06-01

    Lanthanum carbonate is a nonaluminum, noncalcium phosphate-binding agent, which is widely used in patients with end-stage chronic kidney disease. Until now, no significant side-effects have been described for the clinical use of lanthanum carbonate, and there are no available clinical data regarding its tissue stores. Here we report the case of a 59-year-old patient who was admitted with confusional syndrome. The patient received 3750 mg of lanthanum carbonate daily. Examinations were carried out, and the etiology of the encephalopathy of the patient could not be singled out. The lanthanum carbonate levels in serum and cerebrospinal fluid were high, and the syndrome eased after the drug was removed. The results of our study confirm that, in our case, the lanthanum carbonate did cross the blood-brain barrier (BBB). Although lanthanum carbonate seems a safe drug with minimal absorption, this work reveals the problem derived from the increase of serum levels of lanthanum carbonate, and the possibility that it may cross the BBB. Further research is required on the possible pathologies that increase serum levels of lanthanum carbonate, as well as the risks and side-effects derived from its absorption.

  10. Reequilibration of chromite within Kilauea Iki lava lake, Hawaii

    USGS Publications Warehouse

    Scowen, P.A.H.; Roeder, P.L.; Helz, R.T.

    1991-01-01

    Chromite mainly occurs as tiny inclusions within or at the edges of olivine phenocrysts in the 1959 Kilauea Iki lava lake. Liquilus chromite compositions are only preserved in scoria that was rapidly quenched from eruption temperatures. Analyses of drill core taken from the lava lake in 1960, 1961, 1975, 1979, and 1981 show that chromite becomes richer in Fe+2, Fe+3, Ti and poorer in Mg, Al, Cr than the liquidus chromite. The amount of compositional change depends on the time elapsed since eruption, the cooling history of the sample, the extent of differentiation of the interstitial melt, and the position of the chromite inclusion within the olivine phenocryst. Compositional changes of the chromite inclusions are thought to be a result of reequilibration with the residual melt by cationic diffusion (Mg, Al, Cr outwards and Fe+2, Fe+3, Ti inwards) through olivine. The changing chemical potential gradients produced as the residual melt cools, crystallizes and differentiates drives the reequilibration process. Major and minor element zoning profiles in olivine phenocrysts suggest that volume diffusion through olivine may have been the major mechanism of cationic transport through olivine. The dramatic compositional changes observed in chromite over the 22 years between eruption and 1981 has major implications for othe molten bodies. ?? 1991 Springer-Verlag.

  11. Functionally graded doped lanthanum cobalt ferrite and ceria-based composite interlayers for advancing the performance stability in solid oxide fuel cell

    NASA Astrophysics Data System (ADS)

    Ghosh, Koyel Banerjee; Mukhopadhyay, Jayanta; Basu, Rajendra N.

    2016-10-01

    Functionally graded composite interlayer based on 50% of La0.54Sr0.4Co0.2Fe0.8O3-δ and 50% of La0.54Sr0.4Fe0.2Co0.8O3-δ (CF-1) and cobalt and gadolinium doped ceria (CoCGO) is synthesized varying the mass ratio as CF-1:CoCGO = 80:20(L80-C20), 50:50(L50-C50) and 20:80(L20-C80). Detail study using impedance spectroscopy of symmetrical cell fabricated with CoCGO as electrolyte reveals the lowest electrode polarization 0.04 Ω cm2 at 800 °C for L80-C20 composite. Electrode and ohmic polarization is also evaluated configuring the symmetric cell as CF-1/L80-C20||CoCGO||L80-C20/CF-1. Symmetric cell with varying composition of the composite interlayer (L80-C20/L50-C50/L20-C80||CoCGO||L20-C80/L50-C50/L80-C20) shows considerably low electrode polarization of 0.067 Ω cm2 at 800 °C with activation energy 1.19 eV. Electrochemical performances evaluated using single cell configuration Ni-YSZ||YSZ||CoCGO/L20-C80/L50-C50/L80-C20/CF-1 shows power density as high as 2.03 W cm-2 at 800 °C at 0.7 V. Addition of composite interlayers increases the stability significantly and the voltage degradation is found negligible (0.9%) for first 300 h at a constant load of 0.5 A cm-2 which is further increased to 2.9% for next 300 h. The cell stability is clinically correlated with layer wise elemental 'Sr' mapping in the applied quad interlayers.

  12. Fluid-present deformation aids chemical modification of chromite: Insights from chromites from Golyamo Kamenyane, SE Bulgaria

    NASA Astrophysics Data System (ADS)

    Satsukawa, Takako; Piazolo, Sandra; González-Jiménez, José María; Colás, Vanessa; Griffin, William L.; O'Reilly, Suzanne Y.; Gervilla, Fernando; Fanlo, Isabel; Kerestedjian, Thomas N.

    2015-07-01

    Chemical signatures of chromitites are commonly used to track the evolution of the Earth's mantle. However, chemical modification during deformation may have important implications for the interpretation of chromites' signatures. Here, we describe the details of how deformation promotes chemical modification in chromite. Physicochemical characteristics of the chromites were quantified by measuring crystallographic orientation relationships using Electron Back-Scattered Diffraction (EBSD) and electron microprobe analysis (EMP). Chromites show porphyroclastic textures with coarse-grained porphyroclasts (ca. 0.2-5 mm) and fine-grained neoblasts (< 200 μm). Coarse-grained chromites are chemically zoned in terms of major elements from core to rim, preserving this initial igneous feature in the cores, while the outer rims reveal a metamorphic signature. Large chromite grains are characterized by local crystal-plastic deformation, exhibiting distinct inter-crystalline deformation including continuous crystal bending and subgrain boundaries as well as chemical modification in their outer, deformed parts. Two types of fine-grained chromite, F1 and F2, are present. While F1 exhibits a well-developed polygonal texture, straight grain boundaries and low intercrystal misorientation (< 1°), F2 shows low-angle boundaries and significant intercrystalline misorientation (2-8°). Both F1 and F2 have higher Fe3 + and Cr and lower Mg# values than the cores of large grains. We interpret F1 and F2 to represent chromite recrystallized by heterogeneous nucleation and subgrain rotation recrystallization, respectively. Crystallographic preferred orientation (CPO) and misorientation data on the well-developed low-angle (subgrain) boundaries in coarse grains and F2 grains indicate that deformation in chromite was accommodated mainly by dislocation creep with the dominant activation of the {111}<100 > slip system. The retrograde P-T exhumation path predicted by thermodynamic and chemical

  13. The Emma Bell Deposit, Siskiyou Co., California : a possible low-grade source of chromite

    USGS Publications Warehouse

    Lipin, B.R.; Wetzel, Nicholas; Heinrich, S.M.

    1983-01-01

    The Emma Bell chromite deposit in Siskiyou County, California contains over 5 million tons of dunite averaging about 4 percent Cr2O3. Chromite is not evenly disseminated throughout the dunite, however. For the most part the deposit consists of many chromite-rich bands in sharp contact with, and separated by, common dunite containing 1 to 2 percent accessory chromite. Electron microprobe and petrographic analysis of accessory chromite shows that it is fine grained (average grain size 0.14 mm), generally lower in Cr2O3, and has a lower Cr/Fe ratio than segregated chromite. In addition, unusual patchy zoning is exhibited by some accessory chromite. These patchy zones are extremely rich in iron (>60 percent total iron oxide). The negative factors such as the fine-grained nature of the accessory chromite and high iron content compared to segregated chromite, could be overcome by the very large tonnage in the deposit.

  14. Lanthanum Bromide Detectors for Safeguards Measurements

    SciTech Connect

    Wright, J.

    2011-05-25

    Lanthanum bromide has advantages over other popular inorganic scintillator detectors. Lanthanum bromide offers superior resolution, and good efficiency when compared to sodium iodide and lanthanum chloride. It is a good alternative to high purity germanium detectors for some safeguards applications. This paper offers an initial look at lanthanum bromide detectors. Resolution of lanthanum bromide will be compared lanthanum chloride and sodium-iodide detectors through check source measurements. Relative efficiency and angular dependence will be looked at. Nuclear material spectra, to include plutonium and highly enriched uranium, will be compared between detector types.

  15. Thermodynamic properties of higher lanthanum silicide

    SciTech Connect

    Polotskaya, R.I.

    1988-07-01

    The thermodynamic properties of lanthanum disilicide were examined for the first time in the 960-1050/sup 0/K range by measuring the electromotive force of a galvanic cell based on LaSn, the chlorides of potassium, sodium, and lanthanum, and lanthanum silicide and silicon. Reference electrodes were used to prevent lanthanum interaction with the electrolyte. The alloys were melted in an electric arc furnace in purified argon from lanthanum and silicon and followed by two-stage annealing. It was found that the resulting value of the enthalpy formation differed from the estimated value for lanthanum disilicide calculated by Miedema's model.

  16. Co-settling of Chromite and Sulfide Melt Droplets and Trace Element Partitioning between Sulfide and Silicate Melts

    NASA Astrophysics Data System (ADS)

    Manoochehri, S.; Schmidt, M. W.; Guenther, D.

    2013-12-01

    Gravitational settling of immiscible, dense sulfide melt droplets together with other cumulate phases such as chromite, combined with downward percolation of these droplets through a cumulate pile, is thought to be one of the possible processes leading to the formation of PGE rich sulfide deposits in layered mafic intrusions. Furthermore some chromitite seams in the Merensky Reef (Bushveld Complex) are considered to be acting as a filter or barrier for further downward percolation of sulfide melts into footwall layers. To investigate the feasibility of such mechanical processes and to study the partitioning behavior of 50 elements including transition metals and REEs (but not PGEs) between a silicate and a sulfide melt, two separate series of high temperature (1250-1380 °C) centrifuge-assisted experiments at 1000 g, 0.4-0.6 GPa were conducted. A synthetic silicate glass with a composition representative of the parental magma of the Bushveld Complex (~ 55 wt% SiO2) was mixed with pure FeS powder. For the first series of experiments, 15 or 25 wt% natural chromite with average grain sizes of ~ 5 or 31 μm were added to a mixture of silicate glass and FeS (10 wt%) adding 1 wt% water. For the second series, a mixture of the same glass and FeS was doped with 50 trace elements. These mixtures were first statically equilibrated and then centrifuged. In the first experimental series, sulfide melt droplets settled together with, but did not segregate from chromite grains even after centrifugation at 1000 g for 12 hours. A change in initial chromite grain size and proportions didn't have any effect on segregation. Without chromite, the starting mixture resulted in the formation of large sulfide melt pools together with finer droplets still disseminated through the silicate glass and both at the bottom of the capsule. The incomplete segregation of sulfide melt is interpreted as being due to high interfacial energies between sulfide and silicate melts/crystals which hinder

  17. Occupational health assessment of chromite toxicity among Indian miners

    PubMed Central

    Das, Alok Prasad; Singh, Shikha

    2011-01-01

    Elevated concentration of hexavalent chromium pollution and contamination has contributed a major health hazard affecting more than 2 lakh mine workers and inhabitants residing in the Sukinda chromite mine of Odisha, India. Despite people suffering from several forms of ill health, physical and mental deformities, constant exposure to toxic wastes and chronic diseases as a result of chromite mining, there is a tragic gap in the availability of 'scientific’ studies and data on the health hazards of mining in India. Occupational Safety and Health Administration, Odisha State Pollution Control Board and the Odisha Voluntary Health Association data were used to compile the possible occupational health hazards, hexavalent chromium exposure and diseases among Sukinda chromite mines workers. Studies were reviewed to determine the routes of exposure and possible mechanism of chromium induced carcinogenicity among the workers. Our studies suggest all forms of hexavalent chromium are regarded as carcinogenic to workers however the most important routes of occupational exposure to Cr (VI) are inhalation and dermal contact. This review article outlines the physical, chemical, biological and psychosocial occupational health hazards of chromite mining and associated metallurgical processes to monitor the mining environment as well as the miners exposed to these toxicants to foster a safe work environment. The authors anticipate that the outcome of this manuscript will have an impact on Indian chromite mining industry that will subsequently bring about improvements in work conditions, develop intervention experiments in occupational health and safety programs. PMID:21808494

  18. Chlorination of lanthanum oxide.

    PubMed

    Gaviría, Juan P; Navarro, Lucas G; Bohé, Ana E

    2012-03-08

    The reactive system La(2)O(3)(s)-Cl(2)(g) was studied in the temperature range 260-950 °C. The reaction course was followed by thermogravimetry, and the solids involved were characterized by X-ray diffraction, scanning electron microscopy, and energy dispersive spectroscopy. The results showed that the reaction leads to the formation of solid LaOCl, and for temperatures above 850 °C, the lanthanum oxychloride is chlorinated, producing LaCl(3)(l). The formation of the oxychloride progresses through a nucleation and growth mechanism, and the kinetic analysis showed that at temperatures below 325 °C the system is under chemical control. The influence of diffusive processes on the kinetics of production of LaOCl was evaluated by studying the effect of the reactive gas flow rate, the mass of the sample, and the chlorine diffusion through the boundary layer surrounding the solid sample. The conversion curves were analyzed and fitted according to the Johnson-Mehl-Avrami description, and the reaction order with respect to the chlorine partial pressure was obtained by varying this partial pressure between 10 and 70 kPa. The rate equation was obtained, which includes the influence of the temperature, chlorine partial pressure, and reaction degree.

  19. Speciation and recovery of chromium from chromite ore processing residues.

    PubMed

    Sreeram, K J; Ramasami, T

    2001-10-01

    The processing of chromite ore is associated with the generation of large quantities of solid wastes containing chromium, which have been disposed of as landfill for many years. The mobilization and operational speciation of chromium contained in soils contaminated with metal salts are important in terms of the environment. Several methods have been employed for the extraction and recovery of solid wastes. Chromium contained in contaminated soils and solid wastes can be categorized as exchangeable, oxidizable, carbonate-bound, reducible and residual. The results from this study indicate a need for efficient leaching methodologies in chromite ore processing plants to decrease the non-detrital fractions of chromium in the residue. Aggressive methodologies are required to recover chromium from the detrital fractions. The potential benefits of employing sodium peroxide for the complete recovery of chromium from chromite residue have been demonstrated, and the need to ensure the safety of the process has been emphasized.

  20. Sulfuric acid leaching kinetics of South African chromite

    NASA Astrophysics Data System (ADS)

    Zhao, Qing; Liu, Cheng-jun; Shi, Pei-yang; Zhang, Bo; Jiang, Mao-fa; Zhang, Qing-song; Zevenhoven, Ron; Saxén, Henrik

    2015-03-01

    The sulfuric acid leaching kinetics of South African chromite was investigated. The negative influence of a solid product layer constituted of a silicon-rich phase and chromium-rich sulfate was eliminated by crushing the chromite and by selecting proper leaching conditions. The dimensionless change in specific surface area and the conversion rate of the chromite were observed to exhibit a proportional relationship. A modified shrinking particle model was developed to account for the change in reactive surface area, and the model was fitted to experimental data. The resulting model was observed to describe experimental findings very well. Kinetics analysis revealed that the leaching process is controlled by a chemical reaction under the employed experimental conditions and the activation energy of the reaction is 48 kJ·mol-1.

  1. Preparation of porous lanthanum phosphate with templates

    SciTech Connect

    Onoda, Hiroaki; Ishima, Yuya; Takenaka, Atsushi; Tanaka, Isao

    2009-08-05

    Malonic acid, propionic acid, glycine, n-butylamine, and urea were added to the preparation of lanthanum phosphate from lanthanum nitrate and phosphoric acid solutions. All additives were taken into lanthanum phosphate particles. The additives that have a basic site were easy to contain in precipitates. The addition of templates improved the specific surface area of lanthanum phosphate. The amount of pore, with radius smaller than 4 nm, increased with the addition of templates. The remained additives had influence on the acidic properties of lanthanum phosphate.

  2. Impact assessment of chromite mining on groundwater through simulation modeling study in Sukinda chromite mining area, Orissa, India.

    PubMed

    Dhakate, Ratnakar; Singh, V S; Hodlur, G K

    2008-12-30

    The pre-Cambrian chromites ore deposits in Sukinda valley, Jajpur District, Orissa, India, are well known for chromite ore deposits. The exploitation of the ore is carried out through open cast mining method since the last few decades. In the process, the overburden and ore dumps are stored on ground surface, where leaching of chromite and other toxic element takes place particularly during monsoon seasons. This leachate may cause threat to groundwater in the vicinity. An integrated approach has been adopted to evaluate possibility of pollution due to mine seepage and leachate migration on groundwater regime. The approach involves geophysical, hydrogeological, hydro-chemical and aquifer modeling studies. The investigation has the significance as many habitats surround the mining area facing groundwater problems.

  3. Compaction of Chromite Cumulates applying a Centrifuging Piston-Cylinder

    NASA Astrophysics Data System (ADS)

    Manoochehri, S.; Schmidt, M. W.

    2012-12-01

    Stratiform accumulations of chromite cumulates, such as the UG2 chromitite layer in the Bushveld Complex, is a common feature in most of the large layered mafic intrusions. The time scales and mechanics of gravitationally driven crystal settling and compaction and the feasibility of these processes for the formation of such cumulate layers is investigated through a series of high temperature (1280-1300 °C) centrifuge-assisted experiments at 100-2000 g, 0.4-0.6 GPa. A mixture of natural chromite, with defined grain sizes (means of 5 μm, 13 μm, and 52 μm), and a melt with a composition thought to represent the parental magma of the Bushveld Complex, was first chemically and texturally equilibrated at static conditions and then centrifuged. Centrifugation leads to a single cumulate layer formed at the gravitational bottom of the capsule. This layer was analysed for porosity, mean grain size, size distribution and also travelling distance of chromite crystals. The experimentally observed mechanical settling velocity of chromite grains in a suspension with ~ 24 vol% crystals is calculated to be about half (~ 0.53) of the Stokes settling velocity, consistent with a sedimentation exponent n of 2.35±0.3. The settling leads to a porosity of about 52 % in the chromite layer. Formation times of chromite orthocumulates with initial crystal content in the melt of 1 % and grain sizes of 2 mm are thus around 0.6 m/day. To achieve more compacted chromite piles, centrifugation times and acceleration were increased. Within each experiment the crystal content of the cumulate layer increases downward almost linearly at least in the lower 2/3 of the cumulate pile. Although porosity in the lowermost segment of the chromite layer decreases with increasing effective stress integrated over time, the absolute decrease is smaller than for experiments with olivine (from a previous study). Formation times of a ½ meter single chromite layer with 70 vol% chromite, is calculated to be

  4. Ames Lab 101: Lanthanum Decanting

    ScienceCinema

    Riedemann, Trevor

    2016-07-12

    Ames Laboratory scientist Trevor Riedemann explains the process that allows Ames Laboratory to produce some of the purest lanthanum in the world. This and other high-purity rare-earth elements are used to create alloys used in various research projects and play a crucial role in the Planck satellite mission.

  5. DISSOLUTION OF LANTHANUM FLUORIDE PRECIPITATES

    DOEpatents

    Fries, B.A.

    1959-11-10

    A plutonium separatory ore concentration procedure involving the use of a fluoride type of carrier is presented. An improvement is given in the derivation step in the process for plutonium recovery by carrier precipitation of plutonium values from solution with a lanthanum fluoride carrier precipitate and subsequent derivation from the resulting plutonium bearing carrier precipitate of an aqueous acidic plutonium-containing solution. The carrier precipitate is contacted with a concentrated aqueous solution of potassium carbonate to effect dissolution therein of at least a part of the precipitate, including the plutonium values. Any remaining precipitate is separated from the resulting solution and dissolves in an aqueous solution containing at least 20% by weight of potassium carbonate. The reacting solutions are combined, and an alkali metal hydroxide added to a concentration of at least 2N to precipitate lanthanum hydroxide concomitantly carrying plutonium values.

  6. Thermoelectric Properties of Lanthanum Sulfide

    NASA Technical Reports Server (NTRS)

    Wood, C.; Lockwood, R.; Parker, J. B.; Zoltan, A.; Zoltan, L. D.; Danielson, L.; Raag, V.

    1987-01-01

    Report describes measurement of Seebeck coefficient, electrical resistivity, thermal conductivity, and Hall effect in gamma-phase lanthanum sulfide with composition of La3-x S4. Results of study, part of search for high-temperature thermoelectric energy-conversion materials, indicate this sulfide behaves like extrinsic semiconductor over temperature range of 300 to 1,400 K, with degenerate carrier concentration controlled by stoichiometric ratio of La to S.

  7. Multifunctionality of nanocrystalline lanthanum ferrite

    NASA Astrophysics Data System (ADS)

    Rai, Atma; Thakur, Awalendra K.

    2016-05-01

    Nanocrystalline lanthanum ferrite has been synthesized by adopting modified Pechini route. No evidence of impurity or secondary phase has been detected up to the detection of error limit of X-ray diffractometer (XRD). Rietveld refinement of X-ray diffraction pattern reveals orthorhombic crystal system with space group Pnma (62).Crystallite size and lattice strain was found to be ˜42.8nm and 0.306% respectively. Optical band gap was found to be 2.109 eV, by UV-Visible diffused reflectance spectrum (DRS). Brunauer-Emmet-Teller (BET) surface area was found to be ˜3.45 m2/g. Magnetization-hysteresis (M-H) loop was recorded at room temperature (300K) reveals weak ferromagnetism in Nanocrystalline lanthanum ferrite. The weak ferromagnetism in lanthanum ferrite is due to the uncompensated antiferromagnetic spin ordering. Ferroelectric loop hysteresis observed at room temperature at 100Hz depicts the presence of ferroelectric ordering in LaFeO3.Simultanious presence of magnetic and ferroelectric ordering at room temperature makes it suitable candidate of Multiferroic family.

  8. Development of Ceramic Interconnect Materials for SOFC

    SciTech Connect

    Yoon, Kyung J.; Stevenson, Jeffry W.; Marina, Olga A.

    2010-08-05

    Currently, acceptor-doped lanthanum chromite is the state-of-the-art ceramic interconnect material for high temperature solid oxide fuel cells (SOFCs) due to its fairly good electronic conductivity and chemical stability in both oxidizing and reducing atmospheres, and thermal compatibility with other cell components. The major challenge for acceptor-doped lanthanum chromite for SOFC interconnect applications is its inferior sintering behavior in air, which has been attributed to the development of a thin layer of Cr2O3 at the interparticle necks during the initial stages of sintering. In addition, lanthanum chromite is reactive with YSZ electrolyte at high temperatures, forming a highly resistive lanthanum zirconate phase (La2Zr2O7), which further complicates co-firing processes. Acceptor-doped yttrium chromite is considered to be one of the promising alternatives to acceptor-doped lanthanum chromite because it is more stable with respect to the formation of hydroxides in SOFC operating conditions, and the formation of impurity phases can be effectively avoided at co-firing temperatures. In addition, calcium-doped yttrium chromite exhibits higher mechanical strength than lanthanum chromite-based materials. The major drawback of yttrium chromite is considered to be its lower electrical conductivity than lanthanum chromite. The properties of yttrium chromites could possibly be improved and optimized by partial substitution of chromium with various transition metals. During FY10, PNNL investigated the effect of various transition metal doping on chemical stability, sintering and thermal expansion behavior, microstructure, electronic and ionic conductivity, and chemical compatibility with other cell components to develop the optimized ceramic interconnect material.

  9. Conditional estimates of the number of podiform chromite deposits

    USGS Publications Warehouse

    Singer, D.A.

    1994-01-01

    A desirable guide for estimating the number of undiscovered mineral deposits is the number of known deposits per unit area from another well-explored permissive terrain. An analysis of the distribution of 805 podiform chromite deposits among ultramafic rocks in 12 subareas of Oregon and 27 counties of California is used to examine and extend this guide. The average number of deposits in this sample of 39 areas is 0.225 deposits per km2 of ultramafic rock; the frequency distribution is significantly skewed to the right. Probabilistic estimates can be made by using the observation that the lognormal distribution fits the distribution of deposits per unit area. A further improvement in the estimates is available by using the relationship between the area of ultramafic rock and the number of deposits. The number (N) of exposed podiform chromite deposits can be estimated by the following relationship: log10(N)=-0.194+0.577 log10(area of ultramafic rock). The slope is significantly different from both 0.0 and 1.0. Because the slope is less than 1.0, the ratio of deposits to area of permissive rock is a biased estimator when the area of ultramafic rock is different from the median 93 km2. Unbiased estimates of the number of podiform chromite deposits can be made with the regression equation and 80 percent confidence limits presented herein. ?? 1994 Oxford University Press.

  10. Chromites from the Nidar ophiolite and Karzok complex, Transhimalaya, eastern Ladakh: their magmatic evolution

    NASA Astrophysics Data System (ADS)

    Ravikant, V.; Pal, Tapan; Das, Dipankar

    2004-11-01

    In the Indus Suture Zone, Ladakh Transhimalaya, chromites occur in different modes, viz. (a) as disseminations (chromite N1) and massive chromitite (chromite NIC) in dunite of the Nidar ophiolite and (b) as disseminations (chromite NIC2) in metamorphosed gabbro of the Karzok complex. Chromites occur both as cumulus and intercumulus phases and show a resorbed boundary with olivine. XRD study shows their uniform lattice parameters ( a0˜8.33 Å). EPMA scan shows variable Cr 2O 3 content of chromite N1 ranging from 52.7 to 60.4% and restricted Cr 2O 3 content for chromite NIC as 61.0-61.5%. The chromite NIC2 also shows a narrow range of Cr 2O 3 content (56.0-58.2%). A 57Fe Mössbauer spectroscopic investigation shows that chromites have similar iron distribution as: Fe 3+(A), Fe 2+(A) and Fe 2+(B). The iron distribution have been linked to oxidation; the higher Fe 3+/Fe 2+ ratio of chromite NIC (0.67) than that of chromite NIC2 (0.30) suggests higher oxidation of the former than the latter. High Mg-olivine (˜Fo 95), high Cr-chromite (Cr#=80) and Al 2O 3 wt% (12.01-12.22) of chromites from the Nidar ophiolite are typical for a boninitic parentage. The Cr# vs Mg# plot and FeO/MgO in melt (˜0.5) also suggest derivation from the boninitic melt. On the other hand, the chemical signatures of chromite NIC2, Al 2O 3 wt% (14.91-15.21) and FeO/MgO (1.17-1.32) for corresponding melt are very different from a boninitic parentage and may be indicative of a depleted peridotite/MORB type-source. The partitioning of Mg and Fe between coexisting olivine and Cr-spinel in chromite NIC indicates sub-solidus temperatures of around 1000 °C. The differences in chemical composition of chromites as well as parental melts suggest different sources for the Nidar ophiolite and the Karzok complex.

  11. Chromite deposits of the north-central Zambales Range, Luzon, Philippines

    USGS Publications Warehouse

    Rossman, D.L.

    1970-01-01

    Peridotite and gabbro form an intrusive complex which is exposed over an area about 35 km wide and 150 km long in the center of the Zambales Range of western Luzon. The Zambales Complex is remarkable for its total known resources, mined and still remaining, of about 15 million metric tons of chromite ore. Twenty percent of Free World production was obtained from this area between 1950 and the end of 1964; in 1960 production reached a high of 606,103 metric tons of refractory-grade ore, mostly from the Coto mine near Masinloc, and 128,426 metric tons of metallurgical ore from the Acoje mine. The United States imports 80 to 90 percent of its refractory-grade chromite from the Philippines, and its basic refractory technology has been designed upon the chemical and physical characteristics of Coto high-alumina chromite ore. Continuation of this pattern will depend upon discovery of additional ore reserves to replace those depleted by mining. The Zambales Ultramafic Complex is of the alpine type in which lenticular or podiform deposits of chromite lie in peridotite or dunite, mostly near Contacts with gabbroic rocks. Layered structures, foliation, and lineation commonly are well developed and transect boundaries between major rock units, including chromite deposits, at any angle. Accordingly, these structures cannot be used as guides in exploration and mining as they are used in stratiform complexes such as the Bushveld, where chromite layers extend for many miles. Probably 90 percent of the known deposits in the Zambales Complex are located in two belts in its northern part. One zone containing high-aluminua refractory-grade deposits extends northeast from the Coto mine and Chromite Reservation No. I along a peridotite contact with olivine gabbro, and another of high-chromium metallurgical grade chromite extends south through the Zambales and Acoje properties, and swings westward around the south side of Mount Lanai along a peridotite contact with norite. The textures

  12. Effect of Strontium-Doped Lanthanum Vanadate on Crystal Structure, Conductivity and Vanadium Valence State of a La1- x Sr x VO3 Anode in a Reducing Environment

    NASA Astrophysics Data System (ADS)

    Liu, Chi-Yang; Tsai, Shu-Yi; Ni, Chung-Ta; Fung, Kuan-Zong

    2017-04-01

    La1- x Sr x VO3 (where x = 0, 0.1, 0.3, 0.5, 0.7, and 1) exhibits a transition from an antiferromagnetic insulator to a paramagnetic metallic conductor and has been synthesized as a potential anode material for solid oxide fuel cells (SOFCs). La1- x Sr x VO3 was synthesized by a solid-state reaction process followed by heat treatment under a reducing atmosphere (Ar:80/H2:20). X-ray diffraction (XRD) results indicate that LaVO3 was substituted with various amounts of Sr2+ in the cation sublattice. Pure LaVO3 shows an orthorhombic structure. After Sr2+ substitution, a more symmetrical cubic perovskite structure was obtained because the tolerance factor is close to 1. The valence state of the vanadium ions of the La1- x Sr x VO3 was further verified by x-ray photoelectron spectroscopy (XPS). According to the XPS results, when the lanthanum ion was substituted by a strontium ion, the negatively charged defect, SrLa', was compensated for by changing the valence of vanadium from a trivalent to a tetravalent or pentavalent state. The dependence of conduction behavior of La1- x Sr x VO3 on the amount of Sr addition is discussed in terms of the hopping process with super/double exchange interaction and a charge transfer mechanism.

  13. PROMOTED ZINC CHROMITE CATALYSTS FOR HIGHER ALCOHOL SYNTHESIS

    SciTech Connect

    Ms. Xiaolei Sun; Professor George W. Roberts

    2000-06-21

    Work during the report period was concentrated on developing analytical techniques. Thin-layer chromatography (TLC) was used in an attempt to define the best mobile phase to separate the components of ''spent'' tetrahydroquinoline by liquid chromatography in a silica gel column. Conditions have been defined for separating the light gases produced by the reaction of carbon monoxide (CO) and hydrogen (H{sub 2}) over promoted ''zinc chromite'' catalysts. This will be done with a temperature-programmed Carboxen-1000 column, using a thermal conductivity detector for analysis. A Petrocol DM 150 capillary column will be purchased to separate the heavier products, which will be analyzed using a flame ionization detector.

  14. Chromite ore processing residue in Hudson County, New Jersey.

    PubMed Central

    Burke, T; Fagliano, J; Goldoft, M; Hazen, R E; Iglewicz, R; McKee, T

    1991-01-01

    Chromite ore processing residue occurs at over 130 sites in Hudson County, New Jersey. Many of these sites are in urban residential areas. This waste is a result of 70 years of chromate and bichromate chemical manufacturing. At least 15% of the sites contain total chromium concentrations greater than 10,000 mg/kg, with hexavalent content ranging from about 1 to 50%. Continuing leaching of this waste results in yellow-colored surface water runoff and yellow deposits on the soil surface and inside basement walls. The chemistry, environmental fate, health effects, and human exposure potentials for this waste are described. Images FIGURE 1. PMID:1935843

  15. Chromite ore processing residue in Hudson County, New Jersey.

    PubMed

    Burke, T; Fagliano, J; Goldoft, M; Hazen, R E; Iglewicz, R; McKee, T

    1991-05-01

    Chromite ore processing residue occurs at over 130 sites in Hudson County, New Jersey. Many of these sites are in urban residential areas. This waste is a result of 70 years of chromate and bichromate chemical manufacturing. At least 15% of the sites contain total chromium concentrations greater than 10,000 mg/kg, with hexavalent content ranging from about 1 to 50%. Continuing leaching of this waste results in yellow-colored surface water runoff and yellow deposits on the soil surface and inside basement walls. The chemistry, environmental fate, health effects, and human exposure potentials for this waste are described.

  16. Field free, directly heated lanthanum boride cathode

    DOEpatents

    Leung, Ka-Ngo; Moussa, D.; Wilde, S.B.

    1987-02-02

    A directly heated cylindrical lanthanum boride cathode assembly is disclosed which minimizes generation of magnetic field which would interfere with electron emission from the cathode. The cathode assembly comprises a lanthanum boride cylinder in electrical contact at one end with a central support shaft which functions as one electrode to carry current to the lanthanum boride cylinder and in electrical contact, at its opposite end with a second electrode which is coaxially position around the central support shaft so that magnetic fields generated by heater current flowing in one direction through the central support shaft are cancelled by an opposite magnetic field generated by current flowing through the lanthanum boride cylinder and the coaxial electrode in a direction opposite to the current flow in the central shaft.

  17. Field free, directly heated lanthanum boride cathode

    DOEpatents

    Leung, Ka-Ngo; Moussa, David; Wilde, Stephen B.

    1991-01-01

    A directly heated cylindrical lanthanum boride cathode assembly is disclosed which minimizes generation of magnetic fields which would interfere with electron emission from the cathode. The cathode assembly comprises a lanthanum boride cylinder in electrical contact at one end with a central support shaft which functions as one electrode to carry current to the lanthanum boride cylinder and in electrical contact, at its opposite end with a second electrode which is coaxially position around the central support shaft so that magnetic fields generated by heater current flowing in one direction through the central support shaft are cancelled by an opposite magnetic field generated by current flowing through the lanthanum boride cylinder and the coaxial electrode in a direction opposite to the current flow in the central shaft.

  18. Pharmacology of the phosphate binder, lanthanum carbonate.

    PubMed

    Damment, Stephen J P

    2011-01-01

    Studies were conducted to compare the phosphate-binding efficacy of lanthanum carbonate directly with other clinically used phosphate binders and to evaluate any potential adverse pharmacology. To examine the phosphate-binding efficacy, rats with normal renal function and chronic renal failure received lanthanum carbonate, aluminum hydroxide, calcium carbonate, or sevelamer hydrochloride in several experimental models. Lanthanum carbonate and aluminum hydroxide markedly increased excretion of [(32)P]-phosphate in feces and reduced excretion in urine in rats with normal renal function (p < 0.05), indicating good dietary phosphate-binding efficacy. In rats with chronic renal failure, lanthanum carbonate and aluminum hydroxide reduced urinary phosphate excretion to a greater degree and more rapidly than calcium carbonate, which in turn was more effective than sevelamer hydrochloride. The potential to induce adverse pharmacological effects was assessed systematically in mice, rats, and dogs with normal renal function using standard in vivo models. There was no evidence of any adverse secondary pharmacological effects of lanthanum carbonate on the central nervous, cardiovascular, respiratory, or gastrointestinal systems. These studies indicate that lanthanum carbonate is the more potent of the currently available dietary phosphate binders. No adverse secondary pharmacological actions were observed in vivo in a systematic evaluation at high doses.

  19. Pharmacology of the Phosphate Binder, Lanthanum Carbonate

    PubMed Central

    Damment, Stephen JP

    2011-01-01

    Studies were conducted to compare the phosphate-binding efficacy of lanthanum carbonate directly with other clinically used phosphate binders and to evaluate any potential adverse pharmacology. To examine the phosphate-binding efficacy, rats with normal renal function and chronic renal failure received lanthanum carbonate, aluminum hydroxide, calcium carbonate, or sevelamer hydrochloride in several experimental models. Lanthanum carbonate and aluminum hydroxide markedly increased excretion of [32P]-phosphate in feces and reduced excretion in urine in rats with normal renal function (p < 0.05), indicating good dietary phosphate-binding efficacy. In rats with chronic renal failure, lanthanum carbonate and aluminum hydroxide reduced urinary phosphate excretion to a greater degree and more rapidly than calcium carbonate, which in turn was more effective than sevelamer hydrochloride. The potential to induce adverse pharmacological effects was assessed systematically in mice, rats, and dogs with normal renal function using standard in vivo models. There was no evidence of any adverse secondary pharmacological effects of lanthanum carbonate on the central nervous, cardiovascular, respiratory, or gastrointestinal systems. These studies indicate that lanthanum carbonate is the more potent of the currently available dietary phosphate binders. No adverse secondary pharmacological actions were observed in vivo in a systematic evaluation at high doses. PMID:21332344

  20. Synthesis and Characterization of Hydrophilic and Semiconductor Cadmium Chromite Nanostructures

    NASA Astrophysics Data System (ADS)

    Mousavi, Zahra; Salavati-Niasari, Masoud; Soofivand, Faezeh; Esmaeili-Zare, Mahdiyeh; Hamadanian, Masood

    2016-11-01

    Cadmium chromite nanostructures were synthesized in high yield by a simple co-precipitation method. CdCr2O4 nanostructures have been achieved using cadmium nitrate tetrahydrate and CrCl3·6H2O as precursors by a co-precipitation method. The effects of various parameters including alkaline agent, pH value, reaction temperature, and surfactant type were investigated to discover the optimum conditions, and it was found that the size and morphology of products can be affected by these parameters. The structure, morphology and surface chemistry of CdCr2O4 powder were investigated by x-ray diffraction, scanning electron microscopy and energy dispersive x-ray spectroscopy. X-ray diffraction patterns indicated the chromite spinel phase with good crystallinity and an average crystallite size of approximately 20 nm. The hydrophilicity of the calcined oxides was investigated by wetting experiments and the sessile drop technique which were carried out at room temperature in air to determine the surface and interfacial interactions.

  1. Chromite in Lower Pennsylvanian Nuttall sandstone from West Virginia - Possible Blue Ridge province source

    SciTech Connect

    O'Connor, J.T. )

    1989-08-01

    Detrital chromite grains from heavy mineral separates of three samples of the Lower Pennsylvanian Nuttall Sandstone Member of the New River Formation were examined by use of a reflected-light petrographic microscope, a scanning electron microscope, and an electron microprobe. Some textures observed microscopically in the chromite grains are similar to those in chromite grains in dunite from the Blue Ridge province of North Carolina that has undergone regional metamorphism. Additional exsolution features are also observed in the chromites of this study. The major-oxide compositions of the detrital chromite grains vary more widely than those of the chromites of the Blue Ridge, possibly due to a larger sampling base. The detrital grain compositions (Cr/(Cr + Al), Mg/(Mg + Fe{sup +2})) plot near the fields of the Blue Ridge chromites, although the appearance of both more aluminum-rich and magnesium-poor compositions possibly indicate a higher facies of metamorphism than the Blue Ridge samples studied to date.

  2. Gastric mucosal status susceptible to lanthanum deposition in patients treated with dialysis and lanthanum carbonate.

    PubMed

    Ban, Shinichi; Suzuki, Syunji; Kubota, Kenji; Ohshima, Susumu; Satoh, Hideaki; Imada, Hiroki; Ueda, Yoshihiko

    2017-02-01

    Lanthanum carbonate is a popular chemical which is administered for patients with end-stage kidney disease to reduce the absorption of phosphate, and lanthanum deposition in the gastroduodenal mucosa has recently been reported. The aim of this study was to assess whether any histologic changes of the gastric mucosa are related to the deposition of lanthanum. Twenty-four patients who revealed the histology of lanthanum deposition on gastroduodenal biopsy between 2011 and 2014 were included in the study, and their clinical records and gastroduodenal biopsies obtained from 2011 to 2015 were reviewed, adding the review of gastroduodenal biopsies before 2011 if possible. Analysis of the deposited materials by scanning electron microscopy-energy dispersive x-ray spectroscopy was performed for a representative gastric biopsy. All patients were diagnosed as having renal insufficiency due to chronic kidney disease and treated with dialysis for more than 5 years, with confirmation of lanthanum carbonate use for 22 patients. Of 121 gastric biopsies and 10 duodenal ones between 2011 and 2015, 86 gastric biopsies (71.1%) and 3 duodenal biopsies (30%), respectively, revealed histology consistent with lanthanum deposition, which was confirmed by scanning electron microscopy-energy dispersive x-ray spectroscopy analysis for a representative case. The deposition tended to occur in the gastric mucosa with regenerative change, intestinal metaplasia, or foveolar hyperplasia (P<.05). Such mucosal changes were observed in about half of the gastric biopsy samples obtained prior to 2010, in which no lanthanum deposition was identified irrespective of the gastric mucosal status. Although direct association between lanthanum deposition and clinical symptoms is not clear, the evaluation of the gastric mucosal status (prior to administration) seems to be important to predict lanthanum deposition when lanthanum carbonate is administered for patients with chronic kidney disease treated with

  3. Oxidative promoted dissolution of chromite by manganese dioxide and concurrent production of chromate

    NASA Astrophysics Data System (ADS)

    Oze, C.; Bird, D. K.; Fendorf, S.

    2003-12-01

    Chromium release and oxidation from chromite is a potential environmental hazard in sediments and soils and a pathway for soil development (weathering of primary minerals) related to ultramafic rocks and their metamorphic derivatives (serpentinites). Birnessite is a common pedologic mineral in these sediments and soils capable of oxidizing aqueous Cr(III). In this study, the interaction between chromite and birnessite is investigated, with an interest in the potential generation of Cr(VI). Specifically, the effects of chromite suspension density, birnessite suspension density, and pH at a temperature of 25 C in relation to the reaction kinetics were examined. The rate of Cr(VI) in solution increases with increasing chromite suspension densities and decreasing pH, but is independent of birnessite suspension densities at values greater than 20 m2 L-1. The overall rate expression of Cr released and oxidized in solution from chromite can be expressed as d[Cr(VI))]/dt = k­Ý,¦{Chromite}0.69 where k­Ý is 0.0016,¦pH2 ­V 0.025pH + 0.097 uM L m2 L-1, {Chromite} is the chromite suspension density in m2 L-1, birnessite suspension densities are greater than 20 m2 L-1 and pH values are between 3 to 8. Experiments involving serpentine soils containing chromite and birnessite produce Cr(VI) rates consistent with those predicted by the overall rate expression with Cr(VI) rates ranging from 9E-4 to 4.4E-3 uM h-1. Additionally, these experiments demonstrate that serpentine soils are a source of non-anthropogenic Cr(VI).

  4. Sediment-dispersed extraterrestrial chromite traces a major asteroid disruption event.

    PubMed

    Schmitz, Birger; Häggström, Therese; Tassinari, Mario

    2003-05-09

    Abundant extraterrestrial chromite grains from decomposed meteorites occur in middle Ordovician (480 million years ago) marine limestone over an area of approximately 250,000 square kilometers in southern Sweden. The chromite anomaly gives support for an increase of two orders of magnitude in the influx of meteorites to Earth during the mid-Ordovician, as previously indicated by fossil meteorites. Extraterrestrial chromite grains in mid-Ordovician limestone can be used to constrain in detail the temporal variations in flux of extraterrestrial matter after one of the largest asteroid disruption events in the asteroid belt in late solar-system history.

  5. METHOD FOR DISSOLVING LANTHANUM FLUORIDE CARRIER FOR PLUTONIUM

    DOEpatents

    Koshland, D.E. Jr.; Willard, J.E.

    1961-08-01

    A method is described for dissolving lanthanum fluoride precipitates which is applicable to lanthanum fluoride carrier precipitation processes for recovery of plutonium values from aqueous solutions. The lanthanum fluoride precipitate is contacted with an aqueous acidic solution containing dissolved zirconium in the tetravalent oxidation state. The presence of the zirconium increases the lanthanum fluoride dissolved and makes any tetravalent plutonium present more readily oxidizable to the hexavalent state. (AEC)

  6. Crystal-Chemical Correlations in Chromites from Kimberlitic and Non-Kimberlitic Sources.

    NASA Astrophysics Data System (ADS)

    Freckelton, C. N.; Flemming, R. L.

    2009-05-01

    This study explores the utility of micro X-ray diffraction (μXRD) as a tool for diamond exploration, as a compliment to current industry-standard techniques such as electron probe microanalysis (EPMA). Here we examine chromite. As one of the first phases to crystallize in mantle rocks, it is a useful indicator of upper mantle magmatic conditions in rocks that have been sampled by kimberlites. In addition, chromite does not alter easily from chemical and physical weathering processes. As such, chromite is a useful kimberlite indicator mineral in diamond exploration. We present correlations between crystal structure (unit cell) and chemical composition of chromite, (Fe,Mg)[Cr, Al]2O4, using correlated μXRD and EPMA data for 133 chromites from a three source locations: Two kimberlite sources and one non-kimberlitic source from an Archean granite/greenstone terrain. Quantitative analysis was performed using Electron Probe Microanalysis (EPMA) at Mineral Services, South Africa, prior to the loan of the samples. Randomly-oriented chromite grains, approximately 500 μm in diameter, were analyzed as previously mounted for EPMA. Micro X-ray-diffraction was performed using a Bruker D8-Discover Diffractometer, with θ-θ geometry, with CuKα radiation, operating at 40 kV and 40 mA, with nominal beam diameter of 500 μm. The data were collected in omega scan mode. Two dimensional General Area Detector Diffraction System (GADDS) images were collected for 20 minutes per image, and integrated to produce one-dimensional plots of intensity versus 2θ, for subsequent unit cell refinement using CELREF. Although all samples in this study were considered to be 'chromite', a plot of Cr/(Cr+Al) versus Fe2+/(Fe2++Mg) shows extensive substitution among four dominant members: chromite (FeCr2O4), magnesio-chromite (MgCr2O4), spinel (MgAl2O4), and hercynite (FeAl2O4), where Mg and Fe2+ substitute for one another on the tetrahedral site, and Cr and Al substitute for one another on the

  7. Effect of additions of aluminosilicate and silicate materials on the softening temperature of chromite ore

    NASA Astrophysics Data System (ADS)

    Zhdanov, A. V.; Nurmaganbetova, B. N.; Pavlov, V. A.

    2015-07-01

    The temperatures of the beginning and end of softening and the temperature range of softening of the fines of the rich chromite ore of the Donskoy Ore Mining & Processing Plant in Kazakhstan are experimentally determined. The following natural and technical silica-containing materials, which are considered as fluxing additions to decrease the melting temperature of the chromite ore, are investigated: aluminosilicate clays, microsilica, and quartzite of various fractions. The effect of additions of the natural and technical silica-containing materials on the temperatures of the beginning and end of softening and the temperature range of softening of the chromite ore of DODPE is analyzed. The influences of various materials and their fraction compositions on the temperature of softening of the chromite ores are compared.

  8. Stratiform chromite deposit model: Chapter E in Mineral deposit models for resource assessment

    USGS Publications Warehouse

    Schulte, Ruth F.; Taylor, Ryan D.; Piatak, Nadine M.; Seal, Robert R., II

    2012-01-01

    Most environmental concerns associated with the mining and processing of chromite ore focus on the solubility of chromium and its oxidation state. Although trivalent chromium (Cr3+) is an essential micronutrient for humans, hexavalent chromium (Cr6+) is highly toxic. Chromium-bearing solid phases that occur in the chromite ore-processing residue, for example, can effect the geochemical behavior and oxidation state of chromium in the environment.

  9. The Operational Leadership of General Douglas MacArthur in OPERATION CHROMITE

    DTIC Science & Technology

    2007-11-02

    NAVAL WAR COLLEGE Newport, R.I. The Operational Leadership of General Douglas MacArthur in OPERATION CHROMITE by Judie A. Heineman Commander, United...Operations. The contents of this paper reflect my own personal views and are not necessarily endorsed by the Naval War College or the Department of...MacArthur in Operation Chromite 9. Personal Author: Judie Ann Heineman, Commander, United States Navy 10.Type of Report: FINAL 11. Date of Report: 13

  10. Messengers from the deep: Fossil wadsleyite-chromite microstructures from the Mantle Transition Zone

    NASA Astrophysics Data System (ADS)

    Satsukawa, Takako; Griffin, William L.; Piazolo, Sandra; O'Reilly, Suzanne Y.

    2015-11-01

    Investigations of the Mantle Transition Zone (MTZ; 410-660 km deep) by deformation experiments and geophysical methods suggest that the MTZ has distinct rheological properties, but their exact cause is still unclear due to the lack of natural samples. Here we present the first direct evidence for crystal-plastic deformation by dislocation creep in the MTZ using a chromitite from the Luobusa peridotite (E. Tibet). Chromite grains show exsolution of diopside and SiO2, suggesting previous equilibration in the MTZ. Electron backscattered diffraction (EBSD) analysis reveals that olivine grains co-existing with exsolved phases inside chromite grains and occurring on chromite grain boundaries have a single pronounced crystallographic preferred orientation (CPO). This suggests that olivine preserves the CPO of a high-pressure polymorph (wadsleyite) before the high-pressure polymorph of chromite began to invert and exsolve. Chromite also shows a significant CPO. Thus, the fine-grained high-pressure phases were deformed by dislocation creep in the MTZ. Grain growth in inverted chromite produced an equilibrated microstructure during exhumation to the surface, masking at first sight its MTZ deformation history. These unique observations provide a window into the deep Earth, and constraints for interpreting geophysical signals and their geodynamic implications in a geologically robust context.

  11. Palladium, platinum, rhodium, iridium and ruthenium in chromite- rich rocks from the Samail ophiolite, Oman.

    USGS Publications Warehouse

    Page, N.J.; Pallister, J.S.; Brown, M.A.; Smewing, J.D.; Haffty, J.

    1982-01-01

    30 samples of chromitite and chromite-rich rocks from two stratigraphic sections, 250 km apart, through the basal ultramafic member of the Samail ophiolite were spectrographically analysed for platinum-group elements (PGE) and for Co, Cu, Ni and V. These data are reported as are Cr/(Cr + Al), Mg/(Mg + Fe) and wt.% TiO2 for most samples. The chromitite occurs as pods or lenses in rocks of mantle origin or as discontinuous layers at the base of the overlying cumulus sequence. PGE abundances in both sections are similar, with average contents in chromite-rich rocks: Pd 8 ppb, Pt 14 ppb, Rh 6 ppb, Ir 48 ppb and Ru 135 ppb. The PGE data, combined with major-element and petrographic data on the chromitite, suggest: 1) relatively larger Ir and Ru contents and highest total PGE in the middle part of each section; 2) PGE concentrations and ratios do not correlate with coexisting silicate and chromite abundances or chromite compositions; 3) Pd/PGE, on average, increases upward in each section; 4) Samail PGE concentrations, particularly Rh, Pt and Pd, are lower than the average values for chromite-rich rocks in stratiform intrusions. 2) suggests that PGEs occur in discrete alloy or sulphide phases rather than in the major oxides or silicates, and 4) suggests that chromite-rich rocks from the oceanic upper mantle are depleted in PGE with respect to chondrites. L.C.C.

  12. Messengers from the deep: Fossil wadsleyite-chromite microstructures from the Mantle Transition Zone.

    PubMed

    Satsukawa, Takako; Griffin, William L; Piazolo, Sandra; O'Reilly, Suzanne Y

    2015-11-13

    Investigations of the Mantle Transition Zone (MTZ; 410-660 km deep) by deformation experiments and geophysical methods suggest that the MTZ has distinct rheological properties, but their exact cause is still unclear due to the lack of natural samples. Here we present the first direct evidence for crystal-plastic deformation by dislocation creep in the MTZ using a chromitite from the Luobusa peridotite (E. Tibet). Chromite grains show exsolution of diopside and SiO2, suggesting previous equilibration in the MTZ. Electron backscattered diffraction (EBSD) analysis reveals that olivine grains co-existing with exsolved phases inside chromite grains and occurring on chromite grain boundaries have a single pronounced crystallographic preferred orientation (CPO). This suggests that olivine preserves the CPO of a high-pressure polymorph (wadsleyite) before the high-pressure polymorph of chromite began to invert and exsolve. Chromite also shows a significant CPO. Thus, the fine-grained high-pressure phases were deformed by dislocation creep in the MTZ. Grain growth in inverted chromite produced an equilibrated microstructure during exhumation to the surface, masking at first sight its MTZ deformation history. These unique observations provide a window into the deep Earth, and constraints for interpreting geophysical signals and their geodynamic implications in a geologically robust context.

  13. Messengers from the deep: Fossil wadsleyite-chromite microstructures from the Mantle Transition Zone

    PubMed Central

    Satsukawa, Takako; Griffin, William L.; Piazolo, Sandra; O’Reilly, Suzanne Y.

    2015-01-01

    Investigations of the Mantle Transition Zone (MTZ; 410–660 km deep) by deformation experiments and geophysical methods suggest that the MTZ has distinct rheological properties, but their exact cause is still unclear due to the lack of natural samples. Here we present the first direct evidence for crystal-plastic deformation by dislocation creep in the MTZ using a chromitite from the Luobusa peridotite (E. Tibet). Chromite grains show exsolution of diopside and SiO2, suggesting previous equilibration in the MTZ. Electron backscattered diffraction (EBSD) analysis reveals that olivine grains co-existing with exsolved phases inside chromite grains and occurring on chromite grain boundaries have a single pronounced crystallographic preferred orientation (CPO). This suggests that olivine preserves the CPO of a high-pressure polymorph (wadsleyite) before the high-pressure polymorph of chromite began to invert and exsolve. Chromite also shows a significant CPO. Thus, the fine-grained high-pressure phases were deformed by dislocation creep in the MTZ. Grain growth in inverted chromite produced an equilibrated microstructure during exhumation to the surface, masking at first sight its MTZ deformation history. These unique observations provide a window into the deep Earth, and constraints for interpreting geophysical signals and their geodynamic implications in a geologically robust context. PMID:26563583

  14. Steady photodarkening of thulium alumino-silicate fibers pumped at 107 μm: quantitative effect of lanthanum, cerium, and thulium

    NASA Astrophysics Data System (ADS)

    Lupi, Jean-François; Vermillac, Manuel; Blanc, Wilfried; Mady, Franck; Benabdesselam, Mourad; Dussardier, Bernard; Neuville, Daniel R.

    2016-06-01

    By pumping thulium-doped silica-based fibers at 1.07~\\mu m, rapid generation of absorbing centers leads to photo-induced attenuation (PIA). This detrimental effect prevents exploiting laser emissions in the visible and near infrared. We report on the characterization of the PIA versus the fiber core composition, particularly the concentration of thulium (Tm), lanthanum (La) and cerium (Ce) ions. We show that UV emision induced by Tm-Tm energy transfers is the source of photo-darkening, and that lanthanum and cerium are efficient hardeners against PIA.

  15. Occurrence and mineral chemistry of chromite and related silicates from the Hongshishan mafic-ultramafic complex, NW China with petrogenetic implications

    NASA Astrophysics Data System (ADS)

    Ruan, Banxiao; Yu, Yingmin; Lv, Xinbiao; Feng, Jing; Wei, Wei; Wu, Chunming; Wang, Heng

    2016-10-01

    The Hongshishan mafic-ultramafic complex is located in the western Beishan Terrane, NW China, and hosts an economic Ni-Cu deposit. Chromite as accessory mineral from the complex is divided into three types based on its occurrence and morphology. Quantitative electron probe microanalysis (EPMA) have been conducted on the different types of chromites. Type 1 chromite occurs as inclusions within silicate minerals and has relatively homogeneous composition. Type 2 chromite occurs among serpentine, as interstitial phase. Type 3 chromite is zoned and exhibits a sudden change in compositions from core to rim. Type 1 chromite occurs in olivine gabbro and troctolite showing homogeneous composition. This chromite is more likely primary. Interstitial type 2 and zoned type 3 chromite has compositional variation from core to rim and is more likely modified. Abundant inclusions of orthopyroxene, phlogopite and hornblende occur within type 2 and type 3 chromites. The parental melt of type 1 chromite has an estimated composition of 14.5 wt% MgO, 12.3 wt% Al2O3 and 1.9 wt% TiO2 and is characterized by high temperature, picritic affinity, hydrous nature and high Mg and Ti contents. Compositions of chromite and clinopyroxene are distinct from those of Alaskan-type complexes and imply that the subduction-related environment is not reasonable. Post orogenic extension and the early Permian mantle plume are responsible for the emplacement of mafic-ultramafic complexes in the Beishan Terrane. The cores of zoned chromites are classified as ferrous chromite and the rims as ferrian chromite. The formation of ferrian rim involves reaction of ferrous chromite, forsterite and magnetite to produce ferrian chromite and chlorite, or alternaively, the rim can be simply envisioned as the result of external addition of magnetite in solution to the already formed ferrous chromite.

  16. Production of Chromium Oxide from Turkish Chromite Concentrate Using Ethanol

    NASA Astrophysics Data System (ADS)

    Aktas, S.; Eyuboglu, C.; Morcali, M. H.; Özbey, S.; Sucuoglu, Y.

    2015-05-01

    In this study, the possibility of chromium extraction from Turkish chromite concentrate and the production of chromium oxide were investigated. For the conversion of chromium(III) into chromium(VI), NaOH was employed, as well as air with a rate of 20 L/min. The effects of the base amount, fusing temperature, and fusing time on the chromium conversion percentage were investigated in detail. The conversion kinetics of chromium(III) to chromium(VI) was also undertaken. Following the steps of dissolving the sodium chromate in water and filtering, aluminum hydroxide was precipitated by adjusting the pH level of the solution. The chromium(VI) solution was subsequently converted to Cr(III) by the combination of sulfuric acid and ethanol. Interestingly, it was observed that ethanol precipitated chromium as chromium(VI) at mildly acidic pH levels, although this effect is more pronounced for K2Cr2O7 than Na2Cr2O7. On the other hand, in the strongly acidic regime, ethanol acted as a reducing agent role in that chromium(VI) was converted into Cr(III) whereas ethanol itself was oxidized to carbon dioxide and water. Subsequently, chromium hydroxide was obtained by the help of sodium hydroxide and converted to chromium oxide by heating at 800 °C, as indicated in thermo gravimetric analysis (TGA).

  17. PROMOTED ZINC CHROMITE CATALYSTS FOR HIGHER ALCOHOL SYNTHESIS

    SciTech Connect

    Ms. Xiaolei Sun; Professor George W. Roberts

    2001-06-15

    This report describes the analytical protocols that were developed during the last two years to analyze ''spent'' THQ (tetrahydroquinoline) slurry liquid. Identification of the components of the ''spent'' THQ should help to understand the influence of the slurry medium on the methanol synthesis reaction, and on other reactions with THQ as the slurry liquid. Silica gel liquid chromatography and high performance liquid chromatography (HPLC) were used to isolate and purify the major compounds in the ''spent'' slurry liquid. Gas chromatography/mass spectroscopy (GC/MS), Fourier transform infrared (FTIR) and nuclear magnetic resonance (NMR) were applied to identify the major compounds. Methyl-, dimethyl-, and trimethyl-THQ were found to comprise more than 80% of the ''spent'' liquid. The balance was various methylated indoles. A methyl group always is attached to the N atom in the ring structure. Speculative mechanisms are presented that may help to understand the interaction between the catalyst and the alkylated THQ slurry liquid, and the effect of liquid composition on the methanol synthesis reaction. A poster entitled ''Promoted Zinc Chromite Catalyst for Higher Alcohol Synthesis in a Slurry Reactor-2. Spent Liquid Analysis'' was presented at the AIChE National Meeting, Los Angeles, CA, Nov 12-17, 2000.

  18. Biotreatment of chromite ore processing residue by Pannonibacter phragmitetus BB.

    PubMed

    Wang, Yangyang; Yang, Zhihui; Peng, Bing; Chai, Liyuan; Wu, Baolin; Wu, Ruiping

    2013-08-01

    Chromite ore processing residues (COPR) is the source of the Cr(VI) contamination in the environment. Pannonibacter phragmitetus BB was used to treat two different types of COPRs in this research. The water-soluble Cr(VI) of COPR A and B is 3,982.9 and 1,181.4 mg/kg, respectively. In the column biotreatment process, P. phragmitetus BB can reduce Cr(VI) in the leachate to an undetectable level at the flow rate of 1 and 2 ml/min. In the direct biotreatment process, Cr(VI) in the liquid supernatant of COPR A and B decreased from 265 and 200 mg/l to 145 and 40 mg/kg after 240 h of incubation. In one-step and two-step biotreatment processes, Cr(VI) in the liquid supernatant of both COPRs can be reduced to an undetectable level. The toxicity characteristic leaching procedure results indicate that the Cr(VI) concentration of treated COPR A (3.48 mg/l) is lower than the identification standards for hazardous wastes of China (5 mg/l) (GB 5085.6-2007). The information obtained in this study has significance for the application of P. phragmitetus BB to remediate COPR contamination.

  19. Respiratory symptoms and occupational bronchitis in chromite ore miners, Sudan.

    PubMed

    Ballal, S G

    1986-10-01

    Prevalence of respiratory symptoms and chronic bronchitis was determined in a group of 122 subjects (77 exposed miners, 18 partially exposed, 27 controls) working at chromite ore mines in Sudan. The mean ages (+/- s.d.) of the three groups were 36.4 (+/- 7.8), 35.2 (+/- 6.8) and 34.6 (+/- 7.5) years respectively. Methods included a respiratory symptoms questionnaire based on the British Medical Research Council (MRC 1976) questionnaire on respiratory symptoms, determination of FEV1, FVC and FEV1/FVC%. The majority (66%) of the exposed subjects were non-smokers (NS) and 20 (77%) of the 'ever-smokers' (current and ex-smokers) were smokers of less than 15 cigarettes day-1. Respiratory symptoms (cough, phlegm, dyspnoea) were more frequent among the miners and so was chronic bronchitis. The prevalence of the latter was 26% among the miners compared to 11% and 7% among the partially exposed and the controls respectively. These differences could not be accounted for by cigarette smoking. Sixty-five per cent of the miners diagnosed as having asthma, chronic bronchitis or both were non-smokers. Although the values for the FEV1/FVC% remained normal or near the lower limits of the normal range, the mean value was significantly lower among the miners. It was concluded that the mine dust was the prime cause of the respiratory symptoms and chronic bronchitis among the miners.

  20. Sulfidation Kinetics of Natural Chromite Ore Using H2S Gas

    NASA Astrophysics Data System (ADS)

    Ahmad, Sazzad; Rhamdhani, M. Akbar; Pownceby, Mark I.; Bruckard, Warren J.

    2015-04-01

    The kinetics and mechanism of natural chromite (FeCr2O4) sulfidation using 5 pct H2S (balance Ar) gas were studied in the temperature range 1173 K to 1473 K (900 °C to 1200 °C). Reaction products were examined using combined X-ray diffraction, scanning electron microscopy, and energy dispersive X-ray spectroscopy. Results indicated the formation of an outer sulfide-rich layer comprising mixed (Fe,Cr)1- x S and (Cr,Fe)1- x S phases, underlain by a cation-depleted diffusion zone. The kinetics investigation indicated that the reaction rate increased with increasing temperature and that the sulfidation of chromite followed a shrinking unreacted core model. It is proposed that Cr3+ cation diffusion through the reaction product was the rate controlling step with an apparent activation energy of 166 ± 4 kJ mol-1. The calculated activation energy lies between the activation energy for Fe2+ and Cr3+ diffusion through pure chromite spinel and Fe-Cr alloy. Possible reasons for the discrepancy from pure chromite are expected to be the presence of minor Al and Mg in the natural chromite sample, and the partial pressure of oxygen under the reaction conditions used.

  1. Thermodynamic properties of lanthanum in gallium-zinc alloys

    NASA Astrophysics Data System (ADS)

    Dedyukhin, A. S.; Shepin, I. E.; Kharina, E. A.; Shchetinskiy, A. V.; Volkovich, V. A.; Yamshchikov, L. F.

    2016-09-01

    Thermodynamic properties of lanthanum were determined in gallium-zinc alloys of the eutectic and over-eutectic compositions. The electromotive force measurements were used to determine thermodynamic activity and sedimentation technique to measure solubility of lanthanum in liquid metal alloys. Temperature dependencies of lanthanum activity, solubility and activity coefficients in alloys with Ga-Zn mixtures containing 3.64, 15 and 50 wt. % zinc were obtained.

  2. Peculiar histiocytic lesions with massive lanthanum deposition in dialysis patients treated with lanthanum carbonate.

    PubMed

    Haratake, Joji; Yasunaga, Chikao; Ootani, Akifumi; Shimajiri, Shohei; Matsuyama, Atsuji; Hisaoka, Masanori

    2015-06-01

    Pathologic lesions caused by lanthanum carbonate (LC), a recently developed phosphate-binding agent, have not been recorded. A peculiar gastroduodenal histiocytic lesion associated with a mucosal lanthanum overload was reported. Our routine gastrointestinal biopsy series included 6 cases with heavy lanthanum burden in the gastroduodenal mucosa. In addition to routine histopathologic examinations, a series of immunohistochemical analysis and electron microscopic examinations associated with x-ray diffraction and elemental analysis were performed. Six cases, 3 of male and 3 of female individuals with ages from 59 to 69 years, were all patients of end-stage renal diseases managed under dialysis and treated with LC for >21 months. Endoscopic examinations demonstrated gastric erosions in 3, gastric polyps in 2, and duodenal ulcer in 1. In the mucosal layer, there were numerous non-Langerhans cell histiocytes, stained with CD68 but not S100 protein, engulfing a large amount of mineral-like materials. An electron microscopic and elemental analysis revealed a similar distribution of lanthanum and phosphorus in the histiocytes. Long-standing LC administration can cause massive mucosal accumulation of lanthanum in the tissue histiocytes associated with several forms of gastroduodenal lesions. A long-standing outcome is not clear at present; hence, careful follow-up studies of these patients may be needed.

  3. Adsorption of lanthanum to goethite in the presence of gluconate

    SciTech Connect

    Hull, Laurence C.; Sarah Pepper; Sue Clark

    2005-05-01

    Adsorption of Lanthanum to Goethite in the Presence of Gluconic Acid L. C. HULL,1 S. E. PEPPER2 AND S. B. CLARK2 1Idaho National Engineering and Environmental Laboratory, Idaho Falls, ID (hulllc@inel.gov) 2Washington State University, Pullman, WA (spepper@wsu.edu), (s_clark@wsu.edu) Lanthanide and trivalent-actinide elements in radioactive waste can pose risks to humans and ecological systems for many years. Organic complexing agents, from natural organic matter or the degradation of waste package components, can alter the mobility of these elements. We studied the effect of gluconic acid, as an analogue for cellulose degradation products, on the adsorption of lanthanum, representing lanthanide and trivalent-actinide elments, to goethite, representing natural iron minearals and degradation products of waste packages. Batch pH adsorption edge experiments were conducted with lanthanum alone, and with lanthanum and gluconate at a 1:1 mole ratio. Lanthanum concentrations studied were 0.1, 1, and 10 mM, covering a range from 10% to 1000% of the calculated available adsorption sites on goethite. In the absence of gluconate, lanthanum was primarily present in solution as free lanthanum ion. With gluconate present, free lanthanum concentration in solution decreased with increasing pH as step-wise deprotonation of the gluconate molecule increased the fraction lanthanum complexed with gluconate. Adsorption to the goethite surface was represented with the diffuse double-layer model. The number of adsorption sites and the intrinsic binding constants for the surface complexes were estimated from the pH adsorption edge data using the computer code FITEQL 4.0. Two surface reactions were used to fit the adsorption data in the absence of gluconate. A strong binding site with no proton release and a much higher concentration of weak binding sites with release of two protons per lanthanum adsorbed. The adsorption of lanthanum was not measurably affected by the presence of gluconate

  4. Sorption of lanthanum ions by natural clinoptilolite tuff

    NASA Astrophysics Data System (ADS)

    Dampilova, B. V.; Zonkhoeva, E. L.

    2013-08-01

    The equilibrium and kinetics of sorption of lanthanum ions on natural clinoptilolite tuff are studied. It is demonstrated that sorption of lanthanum ions from diluted solutions occurs in micropores of clinoptilolite, and from concentrated solutions in the mesoporous structure of tuff. The main capacity of zeolite tuff is found in the secondary porous structure. The sorption of lanthanum ions is limited by diffusion in tuff grains. Lanthanum ions are regularly distributed in the tuff phase and interact with the Brønsted centers of large clinoptilolite cavities.

  5. Systemic lanthanum is excreted in the bile of rats.

    PubMed

    Damment, Stephen J P; Pennick, Michael

    2007-06-15

    Lanthanum carbonate is a non-calcium-based oral phosphate binder for the control of hyperphosphataemia in patients with chronic kidney disease Stage 5. As part of its pre-clinical safety evaluation, studies were conducted in rats to determine the extent of absorption and routes of excretion. Following oral gavage of a single 1500 mg/kg dose, the peak plasma lanthanum concentration was 1.04+/-0.31 ng/mL, 8 h post-dose. Lanthanum was almost completely bound to plasma proteins (>99.7%). Within 24h of administration of a single oral dose, 97.8+/-2.84% of the lanthanum was recovered in the faeces of rats. Comparing plasma exposure after oral and intravenous administration of lanthanum yielded an absolute oral bioavailability of 0.0007%. Following intravenous administration of lanthanum chloride (0.3 mg/kg), 74.1+/-5.82% of the dose (96.9+/-0.50% of recovered lanthanum) was excreted in faeces in 42 days, and in bile-duct cannulated rats, 10.0+/-2.46% of the dose (85.6+/-2.97% of recovered lanthanum) was excreted in bile in 5 days. Renal excretion was negligible, with <2% of the intravenous dose recovered in urine. These studies demonstrate that lanthanum undergoes extremely low intestinal absorption and that absorbed drug is predominantly excreted in the bile.

  6. [Qualitative and quantitative analysis of various elements in chromite ore by ICP-AES].

    PubMed

    Zhang, Yang; Zheng, Shi-li; Wang, Xiao-hui; Xu, Hong-bin; Zhang, Yi

    2010-01-01

    Kind of the elements in chromite ore was firstly determined by ICP-AES. Twenty nine elements, such as Cr, Fe, Al, Mg, Zn, Ca and Ni, were contained in the chromite sample based on the qualitative analysis. Then the contents of main elements Cr, Fe, Al, Mg, Ca, T, Si, Mn and V were measured. The chromite samples processing procedures have two steps, the first is decomposition by nitrate carbonate and sodium tetraborate at 950 degrees C for 30 min, then leaching by dilute hydrochloric acid at 80 degrees C for 10 min. The method showed satisfactory precision and accuracy with the RSDs between 0.48% and 2.05% and the recovery rates between 90.5% and 111.3%.

  7. Treatability of chromite ore processing waste by leaching.

    PubMed

    Unlü, K; Haskök, S

    2001-06-01

    Developing treatment and disposal strategies and health-based clean-up standards for chromium containing wastes continues to be an important environmental regulatory issue because of the opposing solubility and toxicity characteristics of chromium species under diverse environmental conditions. In this study, leaching characteristics of total Cr and Cr(VI) were investigated using laboratory column studies. The data obtained from the experimental studies were analysed to assess the treatability of chromite ore processing waste (COPW) by leaching and to identify the leaching strategies that enhance mass removal rates of chromium species. COPW used for laboratory soil column studies was obtained from an industrial plant producing sodium chromate in Mersin, Turkey. Laboratory investigations involved chemical characterisation of waste material and column studies. For waste characterisation, U.S. EPA toxicity characterisation leaching procedure (TCLP) was performed on COPW to determine the concentrations of metal species in the TCLP extract. For column studies, various laboratory columns containing plain COPW material, 1:1 COPW/reducing agent (elemental iron or manure) mixture and different type soils (sand, loam and clay) overlain by COPW were subjected to leaching tests using acidic, neutral and alkaline influent water to determine Cr mass leaching efficiencies. Based on the TCLP analyses, COPW is classified as hazardous waste. As a result of comparing the leaching efficiency data from twelve leaching columns, the maximum removal of total Cr was achieved by leaching COPW/manure mixture using acidic (pH 4.78) influent water. The highest Cr(VI) leaching efficiency was achieved in the columns of plain COPW and COPW/manure mixture using highly alkaline (pH 12.0) influent water. The least effective leaching efficiency for both total Cr and Cr (VI) was obtained by leaching plain COPW with neutral (pH 7.0) influent water. Land-disposal of the treated COPW material by mixing

  8. Thermal metamorphism of mantle chromites and the stability of noble-metal nanoparticles

    NASA Astrophysics Data System (ADS)

    González-Jiménez, José M.; Reich, Martin; Camprubí, Antoni; Gervilla, Fernando; Griffin, William L.; Colás, Vanessa; O'Reilly, Suzanne Y.; Proenza, Joaquín A.; Pearson, Norman J.; Centeno-García, Elena

    2015-08-01

    The Loma Baya complex in south-western Mexico is a volume of chromitite-bearing oceanic mantle that records a complex metamorphic history, defined by a first stage of hydrous metamorphism overprinted by a short-lived thermal event associated with an Eocene granite intrusion. During the hydrous metamorphism, the primary magmatic chromite-olivine assemblage was replaced by a secondary, porous intergrowth of Fe2+-rich chromite and chlorite. The heat supplied by an Eocene-age granite intrusion reversed the hydration reaction, producing chromite rims with perfectly developed crystal faces. This third-generation chromite is in equilibrium with highly magnesian (neoformed) olivine and defines a chemical trend analogous to the original magmatic one. The preservation of both reactions in the Loma Baya chromitite provides compelling evidence that the hydration of chromite can be reversed by either prograde metamorphism or any heating event, confirming previous thermodynamic predictions. Understanding these complex features is of particular interest due to the fact that changes in temperature and variable degrees of fluid/rock interaction during metamorphism and intrusion have also significantly affected the chromite-hosted IPGE carrier phases. Here, we propose that the metamorphic fluids involved in the hydrous metamorphism have caused the desulphurization of laurite RuS2, releasing minute particles of Ru-Os-Ir alloys <50 nm in diameter. The following short-lived thermal event that promoted dehydration in the chromitite had the opposite effect on nanoparticle stability, producing a significant coarsening of metal nanoparticles to dimensions larger than a micron. Based on such observations, we argue that IPGE nanoparticles can be exsolved and grown (or coarsen) from sulphide matrices during prograde metamorphism or heating and not exclusively upon cooling under magmatic conditions as it has been previously suggested. These results provide new insights on the relevant role of

  9. Osmium, ruthenium, iridium and uranium in silicates and chromite from the eastern Bushveld Complex, South Africa

    USGS Publications Warehouse

    Gijbels, R.h.; Millard, H.T.; Desborough, G.A.; Bartel, A.J.

    1974-01-01

    Osmium, ruthenium, iridium and uranium contents were determined in eight ortho pyroxene, seven plagioclase, and three chromite mineral separates from the eastern Bushveld Complex. Neutron activation analysis was used to measure the platinum metals, and uranium was determined by a fission track technique. The platinum metals were found to be present within each mine??ral in the proportions Os:Ru:Ir = 1:7:1, while the concentrations of these metals in the minerals are in the ratios orthopyroxene:plagioclase:chromite = 1:16:700. The concentration of uranium was found to range from 11 to 66 ppb (parts per billion) and not to vary significantly from mineral to mineral. The data for the platinum metals are consistent with a model in which the eastern Bushveld Complex was formed by the fractional crystallization of two separately injected magmas. A computer fit of this model to these data indicates that the initial concentrations of Os, Ru and Ir in the first magma were 0.24, 2.0 and 0.21 ppb and in the second magma were 0.16, 1.1 and 0.18 ppb, respectively. The fit also yields the distribution coefficients for the partitioning between the liquid and cumulus orthopyroxene, cumulus plagioclase and cumulus chromite. These coefficients (mineral/liquid) for osmium are 4.5, 66 and 2700; for ruthenium, they are 5, 65 and 2700; and for iridium, they are 4, 60 and 1600. To make this fit, it was necessary to hypothesize the existence of two types of chromite: one type with a large distribution coefficient, presumably formed as a cumulus phase at high temperature, and another, more prevalent type with a smaller distribution coefficient, which may have been formed by postcumulus growth at a lower temperature. This hypothesis is supported by data for coexisting chromite-silicate pairs, which indicate that the chromite grains expelled these platinum metals as they cooled. ?? 1974.

  10. Photoluminescence properties of cerium oxide nanoparticles as a function of lanthanum content

    SciTech Connect

    Deus, R.C.; Cortés, J.A.; Ramirez, M.A.; Ponce, M.A.; Andres, J.; Rocha, L.S.R.; and others

    2015-10-15

    Highlights: • CeO{sub 2} nanoparticles were obtained by microwave-hydrothermal method. • Rietveld refinement reveals a cubic structure. • KOH mineralizer agent exhibit weak agglomeration at low temperature and shorter time. - Abstract: The structural and photoluminescent properties at room temperature of CeO{sub 2} and La-doped CeO{sub 2} particles were undertaken. The obtained particles were synthesized by a microwave-assisted hydrothermal method (MAH) under different lanthanum contents. X-ray diffraction (XRD), Fourier transform infrared (FT-IR), Fourier transform Raman (FT-Raman), Ultra-violet spectroscopy (UV–vis) and photoluminescence (PL) measurements were carried out. XRD revealed that the powders are free of secondary phases and crystallize in the cubic structure. Raman data show that increasing La doping content increase oxygen vacancies due to lattice expansion. The UV/vis absorption spectroscopy suggested the presence of intermediate energy levels in the band gap of structurally ordered powders. Lanthanum addition creates oxygen vacancies and shifts the photoluminescence in the low energy range leading to intense PL emission.

  11. Investigation of ionic conductivity of lanthanum cerium oxide nano crystalline powder synthesized by co precipitation method

    NASA Astrophysics Data System (ADS)

    Tinwala, Hozefa; Shah, Patij; Siddhapara, Kirit; Shah, Dimple; Menghani, Jyoti

    2016-10-01

    Lanthanum (La) doped Ceria (CeO2) electrolyte has attracted considerable interest, as a candidate material for solid oxide fuel cells (SOFCs). The ionic conductivity of La doped CeO2 system (La2Ce2O7) nano-particles synthesized by the co-precipitation method has been investigated. The cubic fluorite structure was observed from the structural analysis of the material. Morphology of the sintered pellets are observed by scanning electron microscope (SEM), respectively. From the results of impedance spectroscopy from temperature range of room temperature to 400 °C, the oxide ion conductivity due to proton charge carrier was observed. Thermogravimetric analysis (TGA) was performed on the material to check stability of phase at high temperature.

  12. Ambi-site substitution of Mn in lanthanum germanate apatites

    SciTech Connect

    Kendrick, E.; Knight, K.S.; Slater, P.R.

    2009-08-05

    A neutron diffraction study at 4 K of the Mn doped lanthanum germanate apatite-type oxide ion conductor of nominal starting composition 'La{sub 9.5}Mn{sub 0.5}(GeO{sub 4}){sub 6}O{sub 2.75}' is reported. The structure was refined in space group P6{sub 3}/m, although high thermal displacement parameters were observed for the oxide ion sites (particularly O3, and O4). Reduced thermal displacement parameters were obtained by splitting the O3 site, and allowing the O4 oxygen to move off site, which may indicate local regions of lower symmetry within the structure. In addition, the data suggested ambi-site substitution of Mn, with it being present on both the Ge site and the La site. Assuming no change in La:Mn:Ge ratio, a composition of La{sub 9.18}Mn{sub 0.28}(GeO{sub 4}){sub 5.8}(MnO{sub 4}){sub 0.2}O{sub 2} was determined. As such there are nominally no interstitial oxide ions, but rather cation vacancies on the La site. Therefore, the high conductivity for this sample is most likely related to the introduction of Frenkel-type defects at higher temperature, as previously proposed for other apatite-type systems containing vacancies on the La site.

  13. Chromite-Plagioclase Assemblages as a New Shock Indicator; Implications for the Shock and Thermal Histories of Ordinary Chondrites

    NASA Technical Reports Server (NTRS)

    Rubin, Alan E.

    2006-01-01

    Chromite in ordinary chondrites (OC) can be used as a shock indicator. A survey of 76 equilibrated H, L and LL chondrites shows that unshocked chromite grains occur in equant, subhedral and rounded morphologies surrounded by silicate or intergrown with metallic Fe-Ni and/or troilite. Some unmelted chromite grains are fractured or crushed during whole-rock brecciation. Others are transected by opaque veins; the veins form when impacts cause localized heating of metal-troilite intergrowths above the Fe-FeS eutectic (988 C), mobilization of metal-troilite melts, and penetration of the melt into fractures in chromite grains. Chromite-plagioclase assemblages occur in nearly every shock-stage S3-S6 OC; the assemblages range in size from 20-300 microns and consist of 0.2-20-micron-size euhedral, subhedral, anhedral and rounded chromite grains surrounded by plagioclase or glass of plagioclase composition. Plagioclase has a low impedance to shock compression. Heat from shock-melted plagioclase caused adjacent chromite grains to melt; chromite grains crystallized from this melt. Those chromite grains in the assemblages that are completely surrounded by plagioclase are generally richer in Al2O3, than unmelted, matrix chromite grains in the same meteorite. Chromite veinlets (typically 0.5-2 microns thick and 10-300 microns long) occur typically in the vicinity of chromite-plagioclase assemblages. The veinlets formed from chromite-plagioclase melts that were injected into fractures in neighboring silicate grains; chromite crystallized in the fractures and the residual plagioclase-rich melt continued to flow, eventually pooling to form plagioclase-rich melt pockets. Chromite-rich chondrules (consisting mainly of olivine, plagioclase-normative mesostasis, and 5-15 vol.% chromite) occur in many shocked OC and OC regolith breccias but they are absent from primitive type-3 OC. They may have formed by impact melting chromite, plagioclase and adjacent mafic silicates during higher

  14. Self-activating and doped tantalate phosphors.

    SciTech Connect

    Nyman, May Devan; Rohwer, Lauren Elizabeth Shea

    2011-01-01

    An ideal red phosphor for blue LEDs is one of the biggest challenges for the solid-state lighting industry. The appropriate phosphor material should have good adsorption and emission properties, good thermal and chemical stability, minimal thermal quenching, high quantum yield, and is preferably inexpensive and easy to fabricate. Tantalates possess many of these criteria, and lithium lanthanum tantalate materials warrant thorough investigation. In this study, we investigated red luminescence of two lithium lanthanum tantalates via three mechanisms: (1) Eu-doping, (2) Mn-doping and (3) self-activation of the tantalum polyhedra. Of these three mechanisms, Mn-doping proved to be the most promising. These materials exhibit two very broad adsorption peaks; one in the UV and one in the blue region of the spectrum; both can be exploited in LED applications. Furthermore, Mn-doping can be accomplished in two ways; ion-exchange and direct solid-state synthesis. One of the two lithium lanthanum tantalate phases investigated proved to be a superior host for Mn-luminescence, suggesting the crystal chemistry of the host lattice is important.

  15. 40 CFR 721.10601 - Lanthanum lead titanium zirconium oxide.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Lanthanum lead titanium zirconium... Specific Chemical Substances § 721.10601 Lanthanum lead titanium zirconium oxide. (a) Chemical substance... titanium zirconium oxide (PMN P-11-273; CAS No. 1227908-26-0) is subject to reporting under this...

  16. 40 CFR 721.10601 - Lanthanum lead titanium zirconium oxide.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Lanthanum lead titanium zirconium... Specific Chemical Substances § 721.10601 Lanthanum lead titanium zirconium oxide. (a) Chemical substance... titanium zirconium oxide (PMN P-11-273; CAS No. 1227908-26-0) is subject to reporting under this...

  17. Preparation of high purity lanthanum compounds for use in fluoride optical fibers

    SciTech Connect

    Ewing, K.J.; Buckner, L.; Jaganathan, J.; Ginther, R.; Aggarwal, I.D. . Optical Sciences Div.)

    1989-02-01

    The preparation of ultra-pure lanthanum nitrate by co-precipitation is described. Preparation of high purity lanthanum carbonate from the pure nitrate is also described. Hydrofluorination of pure lanthanum carbonate produces high purity lanthanum fluoride used in the preparation of heavy metal fluoride glasses.

  18. Characterization of gadolinium and lanthanum oxide films on Si (100)

    NASA Astrophysics Data System (ADS)

    Wu, X.; Landheer, D.; Sproule, G. I.; Quance, T.; Graham, M. J.; Botton, G. A.

    2002-05-01

    High-resolution transmission electron microscopy, electron energy loss spectroscopy, and Auger electron spectroscopy, were used to study gadolinium and lanthanum oxide films deposited on Si (100) substrates using electron-beam evaporation from pressed-powder targets. As-deposited films consist of a crystalline oxide layer and an amorphous interfacial layer. A complicated distinct multilayer structure consisting of oxide layers, silicate layers, and SiO2-rich layers in thick (~30 nm) annealed films has been observed for both gadolinium and lanthanum films. For thinner annealed films (~8 nm), there is no longer a crystalline oxide layer but an amorphous gadolinium or lanthanum silicate layer and an interfacial SiO2-rich layer. The formation of the lanthanum silicate by annealing lanthanum oxide is found to be thermodynamically more favorable than the formation of gadolinium silicate.

  19. Beneficiation of Konya-Beyşehir Chromite for Producing Concentrates Suitable for Industry

    NASA Astrophysics Data System (ADS)

    Öztürk, Fatma Deniz; Abakay Temel, Halime

    2016-09-01

    Turkey has a 6% share of world chromite mining and possesses 25 million tons of reserves. Despite their economic importance, the most important Turkish chromite reserves have not been extensively studied with respect to their composition. In this study, the possibility of upgrading Konya-Beyşehir (Turkey) chromite to produce chromite concentrates suitable for industry is investigated. Two groups of enrichment experiments were made. The effects of some parameters that markedly influence the separation of a shaking table, such as the amplitude and slope of the shaking table and the frequency of strokes were investigated in the first group of experiments, The shaking table experiments were planned and carried out using the statistical methods of Design of Experiments (Yate's and ANOVA) in the second group of experiments. As a result, it was found that a concentrate containing 46.89% Cr2O3 content with a yield of 85.18% was obtained from a feed containing 3.98% Cr2O3 content in 0.2 + 0.1 mm size fraction.

  20. An Exercise in X-Ray Diffraction Using the Polymorphic Transition of Nickel Chromite.

    ERIC Educational Resources Information Center

    Chipman, David W.

    1980-01-01

    Describes a laboratory experiment appropriate for a course in either x-ray crystallography or mineralogy. The experiment permits the direct observation of a polymorphic transition in nickel chromite without the use of a special heating stage or heating camera. (Author/GS)

  1. Natural occurrence and synthesis of two new postspinel polymorphs of chromite

    PubMed Central

    Chen, Ming; Shu, Jinfu; Mao, Ho-kwang; Xie, Xiande; Hemley, Russell J.

    2003-01-01

    A high-pressure polymorph of chromite, the first natural sample with the calcium ferrite structure, has been discovered in the shock veins of the Suizhou meteorite. Synchrotron x-ray diffraction analyses reveal an orthorhombic CaFe2O4-type (CF) structure. The unit-cell parameters are a = 8.954(7) Å, b = 2.986(2) Å, c = 9.891(7) Å, V = 264.5(4) Å3 (Z = 4) with space group Pnma. The new phase has a density of 5.62 g/cm3, which is 9.4% denser than chromite-spinel. We performed laser-heated diamond anvil cell experiments to establish that chromite-spinel transforms to CF at 12.5 GPa and then to the recently discovered CaTi2O4-type (CT) structure above 20 GPa. With the ubiquitous presence of chromite, the CF and CT phases may be among the important index minerals for natural transition sequence and pressure and temperature conditions in mantle rocks, shock-metamorphosed terrestrial rocks, and meteorites. PMID:14645712

  2. Determining the Impactor of the Ordovician Lockne Crater: Oxygen Isotopes in Chromite Versus Sedimentary PGE Signatures

    NASA Astrophysics Data System (ADS)

    Schmitz, B.; Heck, P. R.; Alwmark, C.; Kita, N. T.; Peucker-Ehrenbrink, B.; Ushikubo, T.; Valley, J. W.

    2009-03-01

    Oxygen isotopic results for chromite from the Lockne cCater and new PGE results show that the claims by Tagle and Schmitt (2008, LPSC abstr. #1418) that the Lockne Crater was caused by a nonmagmatic iron meteorite lacks substance entirely.

  3. Magnetic separation studies on ferruginous chromite fine to enhance Cr:Fe ratio

    NASA Astrophysics Data System (ADS)

    Tripathy, Sunil Kumar; Banerjee, P. K.; Suresh, Nikkam

    2015-03-01

    The Cr:Fe ratio (chromium-to-iron mass ratio) of chromite affects the production of chrome-based ferroalloys. Although the literature contains numerous reports related to the magnetic separation of different minerals, limited work concerning the application of magnetic separation to fine chromite from the Sukinda region of India to enhance its Cr:Fe ratio has been reported. In the present investigation, magnetic separation and mineralogical characterization studies of chromite fines were conducted to enhance the Cr:Fe ratio. Characterization studies included particle size and chemical analyses, X-ray diffraction analysis, automated mineral analysis, sink-and-float studies, and magnetic susceptibility measurements, whereas magnetic separation was investigated using a rare earth drum magnetic separator, a rare earth roll magnetic separator, an induced roll magnetic separator, and a wet high-intensity magnetic separator. The fine chromite was observed to be upgraded to a Cr:Fe ratio of 2.2 with a yield of 55.7% through the use of an induced roll magnetic separator and a feed material with a Cr:Fe ratio of 1.6.

  4. A MIXED CHEMICAL REDUCTANT FOR TREATING HEXAVALENT CHROMIUM IN A CHROMITE ORE PROCESSING SOLID WASTE

    EPA Science Inventory

    We evaluated a method for delivering ferrous iron into the subsurface to enhance chemical reduction of Cr(VI) in a chromite ore processing solid waste (COPSW). The COPSW is characterized by high pH (8.5 -11.5), high Cr(VI) concentrations in the solid phase (up to 550 mg kg-1) and...

  5. Lanthanum carbonate: safety data after 10 years.

    PubMed

    Hutchison, Alastair J; Wilson, Rosamund J; Garafola, Svetlana; Copley, John Brian

    2016-12-01

    Despite 10 years of post-marketing safety monitoring of the phosphate binder lanthanum carbonate, concerns about aluminium-like accumulation and toxicity persist. Here, we present a concise overview of the safety profile of lanthanum carbonate and interim results from a 5-year observational database study (SPD405-404; ClinicalTrials.gov identifier: NCT00567723). The pharmacokinetic paradigms of lanthanum and aluminium are different in that lanthanum is minimally absorbed and eliminated via the hepatobiliary pathway, whereas aluminium shows appreciable absorption and is eliminated by the kidneys. Randomised prospective studies of paired bone biopsies revealed no evidence of accumulation or toxicity in patients treated with lanthanum carbonate. Patients treated with lanthanum carbonate for up to 6 years showed no clinically relevant changes in liver enzyme or bilirubin levels. Lanthanum does not cross the intact blood-brain barrier. The most common adverse effects are mild/moderate nausea, diarrhoea and flatulence. An interim Kaplan-Meier analysis of SPD405-404 data from the United States Renal Data System revealed that the median 5-year survival was 51.6 months (95% CI: 49.1, 54.2) in patients who received lanthanum carbonate (test group), 48.9 months (95% CI: 47.3, 50.5) in patients treated with other phosphate binders (concomitant therapy control group) and 40.3 months (95% CI: 38.9, 41.5) in patients before the availability of lanthanum carbonate (historical control group). Bone fracture rates were 5.9%, 6.7% and 6.4%, respectively. After more than 850 000 person-years of worldwide patient exposure, there is no evidence that lanthanum carbonate is associated with adverse safety outcomes in patients with end-stage renal disease.

  6. Lanthanum carbonate: safety data after 10 years

    PubMed Central

    Wilson, Rosamund J; Garafola, Svetlana; Copley, John Brian

    2016-01-01

    Abstract Despite 10 years of post‐marketing safety monitoring of the phosphate binder lanthanum carbonate, concerns about aluminium‐like accumulation and toxicity persist. Here, we present a concise overview of the safety profile of lanthanum carbonate and interim results from a 5‐year observational database study (SPD405‐404; ClinicalTrials.gov identifier: NCT00567723). The pharmacokinetic paradigms of lanthanum and aluminium are different in that lanthanum is minimally absorbed and eliminated via the hepatobiliary pathway, whereas aluminium shows appreciable absorption and is eliminated by the kidneys. Randomised prospective studies of paired bone biopsies revealed no evidence of accumulation or toxicity in patients treated with lanthanum carbonate. Patients treated with lanthanum carbonate for up to 6 years showed no clinically relevant changes in liver enzyme or bilirubin levels. Lanthanum does not cross the intact blood–brain barrier. The most common adverse effects are mild/moderate nausea, diarrhoea and flatulence. An interim Kaplan–Meier analysis of SPD405‐404 data from the United States Renal Data System revealed that the median 5‐year survival was 51.6 months (95% CI: 49.1, 54.2) in patients who received lanthanum carbonate (test group), 48.9 months (95% CI: 47.3, 50.5) in patients treated with other phosphate binders (concomitant therapy control group) and 40.3 months (95% CI: 38.9, 41.5) in patients before the availability of lanthanum carbonate (historical control group). Bone fracture rates were 5.9%, 6.7% and 6.4%, respectively. After more than 850 000 person‐years of worldwide patient exposure, there is no evidence that lanthanum carbonate is associated with adverse safety outcomes in patients with end‐stage renal disease. PMID:27479781

  7. The features of structural transformations in lanthanum manganites La{sub 1−x}A{sub x}MnO{sub 3+δ} (A = Ca, Sr, Ba)

    SciTech Connect

    Sedykh, Vera D.

    2014-10-27

    In this work, the effect of the ionic radius and concentration of a doping element on the features of the structural transformations in polycrystalline lanthanum manganites, La{sub 1−x}A{sub x}MnO{sub 3+δ} (A = Ca, Sr, Ba), has been studied by Mössbauer spectroscopy and X-ray diffraction analysis. For Mössbauer investigations, a small amount of {sup 57}Fe (2 at%) Mössbauer isotope was introduced into the samples. It follows from the analysis of the obtained data that both common features of the structural transformations and differences between them exist in lanthanum manganites depending on ionic radius and concentration of a doping element.

  8. Insight into the Consolidation Mechanism of Oxidized Pellets Made from the Mixture of Magnetite and Chromite Concentrates

    NASA Astrophysics Data System (ADS)

    Zhu, Deqing; Yang, Congcong; Pan, Jian; Zhang, Qiang; Shi, Benjing; Zhang, Feng

    2016-04-01

    To produce more competitive stainless steel products, the utilization of low-cost chromite concentrate is of great importance. In a previous study, a high-quality product pellet (CMP) for blast furnace smelting process made from a mixture of 40 wt pct chromite and 60 wt pct magnetite concentrates was manufactured by a high-pressure grinding rollers pretreatment. In this work, an insight into the consolidation mechanism of CMP is taken in comparison with the oxidized pellets (MP) made from 100 pct magnetite concentrate by adopting the scanning electron microscopy, energy-dispersive spectrometer, and X-ray diffractometer. The mineralogy of the pellets and the morphology of the preheated and roasted mineral particles are demonstrated. To gain better understanding of the consolidation mechanism of CMP, the thermodynamics of chromite-magnetite spinel system and hematite-sesquioxide corundum system in air are considered by using FactSage software. It can be found that the solid-state bonding is the dominant form in the consolidation of CMP, which mainly depends on the recrystallization of hematite, the solid solution bonding in adjacent areas of both magnetite-chromite particles and chromite-chromite particles. The latter two bonds rely on the formation of the miscible sesquioxide and spinel solid solution at the contact areas of particles, which is largely affected by the oxidizability of magnetite and chromite spinels. When more chromite concentrate is blended, the weak bonding among the chromite particles gradually becomes the dominant factor, which will lead to the decrease of the mechanical strength of fired pellets. The presence of a small quantity of siliceous liquid phase in CMP is believed to be beneficial to the hardening by accelerating the ion diffusion rate and forming slag bonds.

  9. Chromite and olivine in type II chondrules in carbonaceous and ordinary chondrites - Implications for thermal histories and group differences

    NASA Technical Reports Server (NTRS)

    Johnson, Craig A.; Prinz, Martin

    1991-01-01

    Unequilibrated chromite and olivine margin compositions in type II chondrules are noted to differ systematically among three of the chondrite groups, suggesting that type II liquids differed in composition among the groups. These differences may be interpreted as indicators of different chemical compositions of the precursor solids which underwent melting, or, perhaps, as differences in the extent to which immiscible metal sulfide droplets were lost during chondrule formation. Because zinc is detectable only in type II chromites which have undergone reequilibration, the high zinc contents reported for chondritic chromites in other studies probably reflect redistribution during thermal metamorphism.

  10. Gallium Lanthanum Sulphide Fibers for Infrared Transmission

    NASA Astrophysics Data System (ADS)

    West, Y. D.; Schweizer, T.; Brady, D. J.; Hewak, D. W.

    Gallium lanthanum sulphide (GLS) glass and fiber have potential for use in both active and passive infrared applications. In this paper the optical, thermal, and other key properties, which are essential for understanding the applications and crucial in the quest for practical fibres, are discussed. Glass preparation by melt-quenchingand subsequent fibre fabrication is described using both rod-in-tube and extruded preforms. Absorptive and scattering losses are explored as they could represent a fundamental limitation to successful device fabrication. Potential passive and active applications are reported and the prospects for a future generation of sulphide fiber-based devices examined.

  11. Filamentation and supercontinuum generation in lanthanum glass

    NASA Astrophysics Data System (ADS)

    Yang, Yuxia; Liao, Meisong; Li, Xia; Bi, Wanjun; Ohishi, Yasutake; Cheng, Tonglei; Fang, Yongzheng; Zhao, Guoying; Gao, Weiqing

    2017-01-01

    A broadband supercontinuum (SC) covering 400-2800 nm in a 20 dB dynamic range is reported in a piece of highly nonlinear, low-dispersion bulk lanthanum glass without employing any lens to focus the pump pulse. The spectrum width obtained in this study is broader than the maximum spectrum width obtained in silica photonic crystal fibers. The filaments and bright conical visible emission patterns of the SC are analyzed. Under optimum pump conditions, an SC conversion efficiency of 75% is obtained. The SC conversion efficiency is confirmed to be stable. Additionally, the relationship between the input peak intensity and the output beam radius is elucidated by simulating the propagation of a Gaussian beam in the bulk lanthanum glass. A 0.20 mm stable laser beam radius at the end of the propagation domain is demonstrated in a certain input peak intensity range. This small value of the beam radius indicates that most of the output power is localized over a small region because of the Kerr focusing effect despite the existence of conical emission in the SC generation by filamentation. The findings of this study are of significance for the development of ultra-broadband SC sources based on bulk glasses and high peak power lasers.

  12. The Oxidation State Of Iron In Chromite As A Record Of Deep Earth Processes

    NASA Astrophysics Data System (ADS)

    McGowan, N.; Griffin, W. L.; Pearson, N.; O'Reilly, S. Y.; Clark, S. M.; Roque-Rosell, J.; Marcus, M.; McCammon, C. A.

    2015-12-01

    Recent work on podiform chromitite from the Luobusa massif, Tibet, suggests that a lithospheric slab containing the chromitite was driven into the Transition Zone (>400 km) after primary crystallisation at shallow depth [1]. Exsolution of coesite and pyroxenes from chromite is believed to reflect conversion from the spinel structure to the ultra-high pressure (UHP) calcium ferrite (CF) polymorph below 400 km [2]. Experimental studies report that UHP polymorphs can have a high affinity for Fe3+, leading to disproportionation of Fe2+ to Fe3+ + Fe0 [3], despite low fO2 as evidenced by inclusions of diamond, native metals and alloys, moissanite, and Cr2+-bearing chromite. Luobusa chromitites may be the first natural example of this phenomenon; one study reported a massive chromitite with higher Fe3+/∑Fe than nodular or disseminated varieties with lower modal chromite [4]. The absence of indicators of oxidation implies that the high Fe3+/∑Fe was not produced by formation or alteration of chromite at Earth's surface. A study using samples from Luobusa and the low-pressure Antalya Complex, Turkey was carried out to investigate relationships between pressure, fO2 and Fe3+/∑Fe. In the first application of μ-X-ray absorption near edge structure (μ-XANES) spectroscopy to measure chromite Fe3+/∑Fe, we constructed calibration curves for the pre-edge centroid and main edge maximum features using Fe3+/∑Fe (from Mössbauer spectroscopy) in synthetic and natural spinels. Pre-edge results show that Fe3+/∑Fe increases with vol.% chromite in chromitites from Luobusa, but not from Antalya (fig. 1). High Fe3+/∑Fe thus appears to be a consequence of crystallographic stabilisation of Fe3+ in the UHP polymorph stable below 400 km, despite low-fO2 conditions. The rapid upwelling of the Luobusa chromitite to the uppermost mantle (<10 Ma) has preserved the high Fe3+/∑Fe in samples where re-equilibration with olivine was limited. [1] McGowan et al., Geology (2015) 43, 179

  13. Fabrication, characterization and electrical conductivity of Ru-doped LaCrO3 dense perovskites

    NASA Astrophysics Data System (ADS)

    Jiao, Handong; Wang, Junxiang; Ge, Jianbang; Zhang, Long; Zhu, Hongmin; Jiao, Shuqiang

    2016-04-01

    Ru-doped lanthanum chromates (LaRuxCr1-xO3) were prepared through a solid-state reaction method. The perovskite pellets with high bulk density over 98% were obtained using the as-prepared LaRuxCr1-xO3 powders as starting materials by spark plasma sintering (SPS) process. The pellets performed high electrical conductivity, which increased with increasing of temperature and ruthenium content (0≤x≤0.10). The activation energy of lanthanum chromate was found to be decreased due to the ruthenium doping.

  14. Diverse Chemical Zoning Trends in Acapulco Chromites: How Many Sources for the Parental Materials?

    NASA Astrophysics Data System (ADS)

    El Goresy, A.; Janicke, J.

    1995-09-01

    Acapulco is considered to be a link between primitive chondritic meteorites and the differentiated achondrites. Its parent body presumably formed by accretion of material of chondritic compositions at an fO2 that lies between that of H- and enstatite chondrites [1]. The accreted chondritic material was subjected 4.557 Gyr ago to peak temperatures close to 1200 degrees C that lead to partial melting and extensive recrystallization [1, 2]. Seven morphologically different types of graphite with large variations in C- and N-isotopic compositions were recently reported from Acapulco [3, 4]. At least four distinct isotopic reservoirs are required to explain the C- and N-isotopic compositions of these graphites [3, 4]. While the silicate minerals in Acapulco have isotopically heavy N (delta^(15)N = + 15 per mil) chromites were found to be isotopically light (delta^(15)N = _ 75 to _ 82 per mil). Chromite occurs in Acapulco in six different assemblages: (1) as inclusions in silicates, (2) in FeNi, (3) in troilite, (4) with FeNi and troilite, (5) with FeNi and silicates, and (6) with troilite and silicates. It is also rarely present as small idiomorphic inclusions in plagioclase. Chromites in contact with silicates display no chemical zoning for Cr, Al, Ti, Fe, Mg, Mn, or Zn to the silicate borders thus indicating high degree of equilibration with the silicate neighbours. The MgO-contents of chromites in metals and troilites (4.74 to 7.2 %) are relatively lower and their compositional ranges are relatively wider than those in contact with silicates (6.1 to 7.69 %). Zoning profiles of MgO and FeO in chromites in all assemblages are quite flat. Chromites in contact with metals and troilite display a variety of zoning patterns of Cr, Al, Ti, and Zn. All these chromite types , however, depict the same MnO zoning trends with low MnO-contents in their cores (0.96 to 2.14 %) than in their rims to metal or troilite (1.7 to 3.1 %). With few exceptions, the zoning behaviour of Cr, Al

  15. Application of lanthanum halide scintillators and low-resolution dense plastics for modern MC&A needs.

    SciTech Connect

    Chung, K.; Belian, A. P.; McKigney E. A.; Russo, P. A.

    2004-01-01

    Recent developments in lanthanum halide scintillators and low-resolution dense plastics give breadth to gamma-ray methods of nuclear material detection suitable for modern MC and A needs. Demanding goals for modernization of MC and A cover both portable and continuous on-line measurement applications that are quantitative for inventory/verification, and that serve those quantitative measurement needs plant-wide. Improved performance (sensitivity and reoslution) is important for portable applications in which a single detector must measure many types of materials. Budget is a major issue for continuous inventory measurements with hundreds or even thousands of detectors placed throughout a facility. Experimentally proven resolution of under 4% for 662 keV {sup 137}Cs gamma rays measured with large cerium-doped LaCl{sub 3} (lanthanum chloride) crystals set a new performance standard for versatile, efficient portable applications comparable in price to NaI(Tl), which has been dominant for decades. While the relatively high cost of crystals remains an obstacle for the application of very large numbers of lanthanum halide scintillators as distributed networked detectors, scintillators made from high-density plastic offer a different type of solution for these gamma-ray measurements. Compared to lanthanum halide crystals they are inexpensive and can be larger in size. Despite lower resolution than NaI(Tl), a quantitative interpretation of the photopeak response of the low-cost dense plastic detectors can be tailored to the unique mechanical and spectral properties of different materials at each of hundreds of fixed on-line locations in a plant. This paper describes the properties and presents experimental results for the two new spectrometer types that, together, bracket NaI(Tl) detectors in both performance and cost, fulfilling modern demands for portable and continuous on-line accountability of uranium and plutonium.

  16. The energetics of lanthanum tantalate materials

    SciTech Connect

    Forbes, Tori Z.; Nyman, May; Rodriguez, Mark A.; Navrotsky, Alexandra

    2010-11-15

    Lanthanum tantalates are important refractory materials with application in photocatalysis, solid oxide fuel cells, and phosphors. Soft-chemical synthesis utilizing the Lindqvist ion, [Ta{sub 6}O{sub 19}]{sup 8-}, has yielded a new phase, La{sub 2}Ta{sub 2}O{sub 7}(OH){sub 2}. Using the hydrated phase as a starting material, a new lanthanum orthotantalate polymorph was formed by heating to 850 {sup o}C, which converts to a previously reported LaTaO{sub 4} polymorph at 1200 {sup o}C. The stabilities of La{sub 2}Ta{sub 2}O{sub 7}(OH){sub 2} (LaTa-OH), the intermediate LaTaO{sub 4} polymorph (LaTa-850), and the high temperature phase (LaTa-1200) were investigated using high-temperature oxide melt solution calorimetry. The enthalpy of formation from the oxides were calculated from the enthalpies of drop solution to be -87.1{+-}9.6, -94.9{+-}8.8, and -93.1{+-}8.7 kJ/mol for LaTa-OH, LaTa-850, and LaTa-1200, respectively. These results indicate that the intermediate phase, LaTa-850, is the most stable. This pattern of energetics may be related to cation-cation repulsion of the tantalate cations. We also investigated possible LnTaO{sub 4} and Ln{sub 2}Ta{sub 2}O{sub 7}(OH){sub 2} analogues of Ln=Pr, Nd to examine the relationship between cation size and the resulting phases. - Graphical abstract: The energetics of three lanthanum tantalates were investigated by the high-temperature oxide melt solution calorimetry. The enthalpies of formation from the oxides were calculated from the enthalpies of drop solution to be -87.1{+-}9.6, -94.9{+-}8.8, and -93.1{+-}8.7 kJ/mol for La{sub 2}Ta{sub 2}O{sub 7}(OH){sub 2}, LaTaO{sub 4} (850 {sup o}C), and LaTaO{sub 4} (1200 {sup o}C), respectively. These results indicate that the intermediate phase, LaTaO{sub 4} (850 {sup o}C), is the most stable in energy. Display Omitted

  17. Comparative Planetary Mineralogy: Co, Ni Systematics in Chromite from Planetary Basalts

    NASA Technical Reports Server (NTRS)

    Karner, J. M.; Shearer, C. K.; Papike, J. J.; Righter,K.

    2005-01-01

    Spinel is a minor but important phase in planetary basalts because its variable composition often reflects basalt petrogenesis. For example, complicated zoning trends in spinel can give clues to melt evolution [1], and V concentrations in chromite lend insight into magma oxygen fugacity (fO2) conditions [2]. Nickel and Co are two elements that are commonly used as a measure of melt fractionation, and their partitioning between olivine and melt is fairly well understood. Less clear is their partitioning into spinel, although [3] has explored Ni and Co systematics in experimental charges. This study documents Ni and Co behavior in early crystallizing spinel (chromite) from several planetary basalts in an attempt to compare our results with [3], and also gain insight into basalt evolution on the three planets.

  18. Carbothermic Reduction of Chromite Ore Under Different Flow Rates of Inert Gas

    NASA Astrophysics Data System (ADS)

    Chakraborty, Dolly; Ranganathan, S.; Sinha, S. N.

    2010-02-01

    The reduction of chromite ore with carbon has been studied extensively in many laboratories. Inert gases have been used in these investigations to control the experimental conditions. However, little information is available in the literature on the influence of the gas flow rate on the rate of reduction. Experiments were carried out to study the influence of the flow rate of inert gas on the reducibility of chromite ore. The experiments showed that the rate of reduction increased with the increasing flow rate of argon up to an optimum flow rate. At higher flow rates, the rate of reduction decreased. The influence of the proportion of reductant on the extent of reduction depended on the rate of flow rate of inert gas. The experimental results are interpreted on the basis of a model that postulates that the mechanism of reduction changes with the flow rate of argon.

  19. A new method for the treatment of chromite ore processing residues.

    PubMed

    Wang, Tiangui; He, Menglin; Pan, Qian

    2007-10-22

    Chromite ore processing residue (COPR), derived from the so-called high-lime processing of chromite ore, contains a significant fraction of a leachable Cr(VI) which is harmful to human being and other organisms. In recent years, the concern over environmental pollution from the waste residue containing Cr(VI) has become a major problem for the chromium chemical industry. The main purpose of this investigation is to evaluate a new method for remediation of Cr(VI) in COPR. COPR was mixed with reductants, sucrose, starch or flour, and was calcinated at elevated temperatures in inertial gas. Effects of temperature, dosages of reductants and time on Cr(VI) reduction were investigated. Above 500 degrees C, Cr(VI) can be completely reduced to Cr(III).

  20. Clinical pharmacokinetics of the phosphate binder lanthanum carbonate.

    PubMed

    Damment, Stephen J P; Pennick, Michael

    2008-01-01

    Lanthanum carbonate is considered to be the most potent of a new generation of noncalcium phosphate binders used to treat hyperphosphataemia in chronic kidney disease (CKD), a condition associated with progressive bone and cardiovascular pathology and a markedly elevated risk of death. Its phosphate-binding action involves ionic binding and precipitation of insoluble complexes within the lumen of the intestine, thereby preventing absorption of dietary phosphate. While pharmacokinetics have little relevance to the efficacy of lanthanum carbonate, they are of fundamental importance when it comes to evaluating safety. When administered as lanthanum carbonate, the oral bioavailability of lanthanum is low (approximately 0.001%). The small absorbed fraction is excreted predominantly in bile, with less than 2% being eliminated by the kidneys. Predictably, therefore, plasma exposure and pharmacokinetics have been shown to be similar in healthy human volunteers and CKD stage 5 patients. With almost complete plasma protein binding, free lanthanum concentrations in patients at steady state are <3 pg/mL. These properties greatly reduce systemic exposure, tissue deposition and the potential for adverse effects. While lanthanum has a variety of calcium-like actions in vitro, there is little or no evidence that these occur in vivo. This paradox is explained by the very low concentrations of circulating free lanthanum ions, which are many orders of magnitude lower than reported effect concentrations in vitro. Safety pharmacology and toxicology evaluations have failed to reveal any significant calcium-like actions in vivo, despite inclusion of high intravenous doses in some cases.Lanthanum carbonate has a low propensity to cause systemic drug interactions due to its poor absorption. However, the higher concentrations present in the gastrointestinal tract can form chelates with some drugs, such as fluoroquinolones, and reduce their absorption. The improved understanding of the

  1. Diminiode thermionic energy conversion with lanthanum-hexaboride electrodes

    NASA Technical Reports Server (NTRS)

    Kroeger, E. W.; Bair, V. L.; Morris, J. F.

    1978-01-01

    Thermionic conversion data obtained from a variable gap cesium diminiode with a hot pressed, sintered lanthanum hexaboride emitter and an arc melted lanthanum hexaboride collector are presented. Performance curves cover a range of temperatures: emitter 1500 to 1700 K, collector 750 to 1000 K, and cesium reservoir 370 to 510 K. Calculated values of emitter and collector work functions and barrier index are also given.

  2. Investigation of nanocrystalline zinc chromite obtained by two soft chemical routes

    SciTech Connect

    Gingasu, Dana; Mindru, Ioana; Culita, Daniela C.; Patron, Luminita; Calderon-Moreno, Jose Maria; Preda, Silviu; Oprea, Ovidiu; Osiceanu, Petre; Morena Pineda, Eufemio

    2014-01-01

    Graphical abstract: - Highlights: • Two soft chemical routes to synthesize zinc chromites are described. • Glycine is used as chelating agent (precursor method) and fuel (solution combustion method). • The synthesized chromites have crystallite size in the range of 18–27 nm. • An antiferromagnetic (AFM) transition is observed at about T{sub N} ∼ 18 K. - Abstract: Zinc chromite (ZnCr{sub 2}O{sub 4}) nanocrystalline powders were obtained by two different chemical routes: the precursor method and the solution combustion method involving glycine-nitrates. The complex compound precursors, [ZnCr{sub 2}(NH{sub 2}CH{sub 2}COO){sub 8}]·9H{sub 2}O and [ZnCr{sub 2}(NH{sub 2}CH{sub 2}COOH){sub 4.5}]·(NO{sub 3}){sub 8}·6H{sub 2}O, were characterized by chemical analysis, infrared spectroscopy (IR), ultraviolet–visible spectroscopy (UV–vis) and thermal analysis. The structure, morphology, surface chemistry and magnetic properties of ZnCr{sub 2}O{sub 4} powders were investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), infrared and Raman spectroscopy (RS), ultraviolet–visible spectroscopy (UV–vis) and magnetic measurements. X-ray diffraction patterns indicated the chromite spinel phase with good crystallinity and an average crystallite size of approximately 18–27 nm. The band gap values ranged between 3.31 and 3.33 eV. The magnetic measurements indicated an antiferromagnetic transition at T{sub N} ∼ 17.5/18 K.

  3. Role of quantitative mineralogical analysis in the investigation of sites contaminated by chromite ore processing residue.

    PubMed

    Hillier, S; Roe, M J; Geelhoed, J S; Fraser, A R; Farmer, J G; Paterson, E

    2003-06-01

    A range of techniques, normally associated with mineralogical studies of soils and sediments, has been used to characterise the solid materials found on sites contaminated with chromite ore processing residue (COPR). The results show that a wide range of minerals are present, many of which are found extensively in high-temperature synthetic systems such as cements and clinkers and their low temperature hydration products. Thus, the minerals in COPR can be divided into three main categories: unreacted feedstock ore (chromite); high temperature phases produced during chromium extraction (brownmillerite, periclase and larnite); and finally, minerals formed under ambient weathering conditions on the disposal sites (brucite, calcite, aragonite, ettringite, hydrocalumite, hydrogarnet). Apart from chromite, chromium occurs in brownmillerite, ettringite, hydrocalumite and hydrogarnet. Detailed study of the chemistry and stoichiometry of chromium-bearing phases in conjunction with phase abundance provides a quantitative description of the solid state speciation of Cr(III) and Cr(VI) in and amongst these minerals and in the COPR as a whole. Of the total chromium present in the samples most, approximately 60-70% is present as Cr(III) in chromite, whilst brownmillerite also represents a significant reservoir of Cr(III) which is approximately 15% of the total. The remaining chromium, between 20 and 25%, is present as Cr(VI) and resides mainly in hydrogarnet, and to a slightly lesser extent in hydrocalumite. In the latter, it is present principally in an exchangeable anionic form. Chromium (VI) is also present in ettringite, but quantitatively ettringite is a much less important reservoir of Cr(VI), accounting for approximately 3% of total chromium in one sample, but less than 1% in the other two. This description provides insight into the processes likely to control the retention and release of Cr(VI) from COPR-contaminated sites. Such information is of particular value in

  4. Peridotite hosted chromite, magnesite and olivine deposits of West Anatolia: A review

    NASA Astrophysics Data System (ADS)

    Zedef, Veysel

    2016-04-01

    Turkey has important chromite, magnesite and olivine deposits within peridotite host rocks. The peridotites (harzburgite, verlite, lherzolite and dunite) are mostly serpentinised as a result of metasomatic reaction of olivine and pyroxene minerals with percolating water. The serpentinites are generally an important part of ophiolitic complexes which displays a discontinuous belts all over the country. The chromite deposits are often related to cumulates and tectonites (as Alpine and/or podiform type deposits) and despite their small reserves, their grade can reach up to 58 %. In most deposits, a little enrichment efforts, the grade of chromite can easily be reached from 25 % to 40-45 %. The magnesite deposits of West Anatolia is especially concentrated in three provinces. These provinces are Konya, Kutahya and Eskisehir. The magnesites are of cryptocrystalline type and, like chromite deposits, their reserve are small but have high grade with low FeO-CaO and high MgO ratio. Once again, these deposits are found within serpentinised peridotites of ultramafic belts. The total (proven and inferred) magnesite reserves are approximately 200 million tons, and these are mostly cryptocrystalline character. A small amount of sedimentary magnesite deposits also present in Denizli (SW Anatolia) and Erzincan (Eastern Anatolia). The olivine deposits are found within peridotites of Western Anatolia. Especially, the Kızıldag olivine deposits (located between the border of Antalya and Konya provinces) are noteworthy with its huge (9 billion tons) reserves. The main olivine mineral is forsterite (Mg2SiO4) which has economically important when compared to other olivine mineral fayalite. The deposits have no quality problem but have a serious disadvantages since its location far from the ports and railway stations.

  5. Phase Stability of the Lanthanum Strontium Manganites

    NASA Astrophysics Data System (ADS)

    Zheng, Feng; Pederson, Larry

    1996-03-01

    Phase diagram and thermodynamic data of the La-Sr-Mn-O system has been studied. The ABO3 -type perovskite of this system is presently the preferred cathode material for application in solid oxide fuel cells. And the phase stability of the lanthanum strontium manganites at elevated temperature is vital to fuel cell operation. Measuring the electromotive force through solid galvanic cell (-) Air,Pt|SrF_2,SrO||CaF_2||La_1-xSr_xMnO_3,SrF_2|Pt,Air (+) and the like enable us to derive the strontium oxide activity and other thermodynamic parameters such as Gibbs free energy of reaction, etc, which help us to understand the materials in using.

  6. Postmortem Study of a Magnesia-Chromite Brick from a Lead Recycling Furnace

    NASA Astrophysics Data System (ADS)

    Gregurek, D.; Reinharter, K.; Reiter, V.; Wenzl, C.; Spanring, A.

    2015-09-01

    This study provides an example of a detailed postmortem analysis carried out on a used silicate-bonded magnesia-chromite brick out of a lead recycling furnace. The magnesia-chromite brick suffered from a high chemical attack due to the process slag. The high CaO, BaO, and sulfur-bearing silicate slag, as well as a high Na2O supply from soda resulted not only in a deep-reaching infiltration of the brick microstructure but also in a severe corrosion of the brick components. Both the sintered magnesia and chromite were attacked chemically. The FactSage calculations showed the formation of high amounts of liquid phase in the infiltrated microstructure and the formation of various Na-Ca-Al-silicates. A detailed investigation of the wear mechanisms through "postmortem studies" is a crucial prerequisite for every refractory producer to understand the interactions between slag and refractory materials. The obtained information and insights serve as a basis for improving refractory materials (i.e., choice of refractories for individual process and new developments) and consequently furnace operations (i.e., prolonged furnace campaigns).

  7. The Effect of Carbonaceous Reductant Selection on Chromite Pre-reduction

    NASA Astrophysics Data System (ADS)

    Kleynhans, E. L. J.; Beukes, J. P.; Van Zyl, P. G.; Bunt, J. R.; Nkosi, N. S. B.; Venter, M.

    2016-12-01

    Ferrochrome (FeCr) production is an energy-intensive process. Currently, the pelletized chromite pre-reduction process, also referred to as solid-state reduction of chromite, is most likely the FeCr production process with the lowest specific electricity consumption, i.e., MWh/t FeCr produced. In this study, the effects of carbonaceous reductant selection on chromite pre-reduction and cured pellet strength were investigated. Multiple linear regression analysis was employed to evaluate the effect of reductant characteristics on the aforementioned two parameters. This yielded mathematical solutions that can be used by FeCr producers to select reductants more optimally in future. Additionally, the results indicated that hydrogen (H)- (24 pct) and volatile content (45.8 pct) were the most significant contributors for predicting variance in pre-reduction and compressive strength, respectively. The role of H within this context is postulated to be linked to the ability of a reductant to release H that can induce reduction. Therefore, contrary to the current operational selection criteria, the authors believe that thermally untreated reductants (e.g., anthracite, as opposed to coke or char), with volatile contents close to the currently applied specification (to ensure pellet strength), would be optimal, since it would maximize H content that would enhance pre-reduction.

  8. The Effect of Carbonaceous Reductant Selection on Chromite Pre-reduction

    NASA Astrophysics Data System (ADS)

    Kleynhans, E. L. J.; Beukes, J. P.; Van Zyl, P. G.; Bunt, J. R.; Nkosi, N. S. B.; Venter, M.

    2017-04-01

    Ferrochrome (FeCr) production is an energy-intensive process. Currently, the pelletized chromite pre-reduction process, also referred to as solid-state reduction of chromite, is most likely the FeCr production process with the lowest specific electricity consumption, i.e., MWh/t FeCr produced. In this study, the effects of carbonaceous reductant selection on chromite pre-reduction and cured pellet strength were investigated. Multiple linear regression analysis was employed to evaluate the effect of reductant characteristics on the aforementioned two parameters. This yielded mathematical solutions that can be used by FeCr producers to select reductants more optimally in future. Additionally, the results indicated that hydrogen (H)- (24 pct) and volatile content (45.8 pct) were the most significant contributors for predicting variance in pre-reduction and compressive strength, respectively. The role of H within this context is postulated to be linked to the ability of a reductant to release H that can induce reduction. Therefore, contrary to the current operational selection criteria, the authors believe that thermally untreated reductants ( e.g., anthracite, as opposed to coke or char), with volatile contents close to the currently applied specification (to ensure pellet strength), would be optimal, since it would maximize H content that would enhance pre-reduction.

  9. Lutetium-doped EuO films grown by molecular-beam epitaxy

    SciTech Connect

    Melville, A.; Heeg, T.; Mairoser, T.; Schmehl, A.; Shai, D. E.; Monkman, E. J.; Harter, J. W.; Hollaender, B.; Schubert, J.; Shen, K. M.; Mannhart, J.; Schlom, D. G.

    2012-05-28

    The effect of lutetium doping on the structural, electronic, and magnetic properties of epitaxial EuO thin films grown by reactive molecular-beam epitaxy is experimentally investigated. The behavior of Lu-doped EuO is contrasted with doping by lanthanum and gadolinium. All three dopants are found to behave similarly despite differences in electronic configuration and ionic size. Andreev reflection measurements on Lu-doped EuO reveal a spin-polarization of 96% in the conduction band, despite non-magnetic carriers introduced by 5% lutetium doping.

  10. Massive Chromite in the Brenham Pallasite and the Fractionation of Cr During the Crystallization of Asteroidal Cores

    NASA Technical Reports Server (NTRS)

    Wasson, John T.; Lange, David E.; Francis, Carl A.; Ulff-Moller, Finn

    1999-01-01

    Large (greater than or equal to 2 mm) chromite grains are present in IIIAB iron meteorites and in the main-group a pallasites (PMG), closely related to high-Au IIIAB irons, Pallasites seem to have formed by the intrusion of a highly evolved metallic magma from a IIIAB-like core into fragmented olivine of the overlying dunite mantle. High Cr contents are commonly encountered during the analyses of metallic samples of high-Au IIIAB irons and main-group pallasites, an indication that Cr contents were high in the intruding liquid and that Cr behaved as an incompatible element during the crystallization of the IIIAB magma, contrary to expectations based on the negative IIIAB Cr-Ni and Cr-Au trends among low-Au IIIAB irons. In a region about 10 cm across in the Brenham main-group pallasite massive chromite fills the interstices between olivine grains, the site normally occupied by metal in Brenham and other pallasites. The massive chromite may have formed as a late cumulus phase; because Fe-Ni was also crystallizing, its absence in the chromite-rich region suggests a separation associated with differences in liquid buoyancy. The coexisting chromite and olivine are zoned; in the olivine FeO is highest in pallasitic (olivine-metal) regions, lowest in rims adjacent to chromite, and intermediate in the cores of these olivines. Chromite shows the opposite zoning, with the highest FeO contents at grain edges adjacent to olivine. The observed gradients are those expected to form by Fe-Mg exchange between olivine and chromite during slow cooling at subsolidus temperatures. Compared to normal Brenham, contents of phosphoran olivine and phosphates are higher in the chromitic pallasitic region. We also report data for large-to-massive chromites present in PMG Molong and in high-Au IIIAB Bear Creek that, like Brenham, formed from a highly evolved magma. The Bear Creek chromite has a much lower Mg content than that in the pallasites, implying that, in the PMG, the Mg was extracted

  11. The first occurrence of platinum group minerals (PGM) in a chromite deposit in the Eastern Desert, Egypt

    NASA Astrophysics Data System (ADS)

    Elhaddad, M. A.

    1996-07-01

    The platinum-group mineralogy (PGM) of the chromitite from Gebel Lawi, in the southeastern desert has been investigated. The most abundant base metal sulfides (BMS) associated with the Lawi chromite are pentlandite, millerite and heazlewoodite. The major platinum-group minerals identified were as follows: laurite (IrOsRu)S2, osmian iridium (OsIr), hollingworthite (RhAsS), tellurian arsenopalladinite (PdTeSbAs), potarite (PdHg) besides cuprian palladian gold (CuPdAu), a Pd-Sb-Hg and HgTe phases. Laurite and osmian iridium occur preferentially in chromite. Os-Ir commonly forms composite PGM with laurite. Hollingworthite and tellurian arsenopalladinite are included within serpentine and, close to the base-metal sulfides, the cuprian palladian gold shares boundaries with chromite. Potarite together with the Pd-Sb-Hg and HgTe phases are embedded in serpentine. Palladium is the most abundant PGE in the Gebel Lawi chromite. A paragenetic sequence of PGM formation is described. Textural evidence indicates that Os-, Ir- and Ru-bearing PGM formed early and were followed by Rh- and Pd-bearing PGM. The concentration of all five PGE could be magmatic, but much of the PGE mineralogy except for laurite and osmian iridium in the center of chromite grains, has been modified by subsequent processes. At later stages, the environment became Te-, Sb-, As- and Hg-rich, which finally led to the formation of low-temperature alteration minerals.

  12. The Dongbo and Purang ultramafic massifs in the Yarlung Zangbo suture zone of Tibet: Prospects for large chromite deposits

    NASA Astrophysics Data System (ADS)

    Xiong, F.; Yang, J.; Li, Y.; Liu, Z.; Liu, F.; Xu, X.

    2012-12-01

    Many ultramafic massifs occur along the Neo-Tethyan Yarlung Zangbo suture zone between the Indian and Eurasian plates, and the Dongbo and Purang ultramafic massifs in the western part of the zone are two of the largest. Both of them consist mainly of high-Mg harzburgite (with low pyroxene contents) and dunite with minor lherzolite. Mineral compositions of olivine, orthopyroxene, clinopyroxene, and chromite, as well as whole-rock petrochemistry indicate that these are typical Alpine-type mantle peridotites. Chromium spinels in the lherzolite have Cr#s (=100 x Cr/(Cr+Al)) of 20-30, showing an affinity with abyssal peridotites, whereas those in the harzburgites have Cr#s ranging from 20 to 75, implying later melt-rock reaction. Based on the mineralogy and geochemistry of the rocks, the Dongbo and Purang massifs are interpreted as fragments of MORB lithosphere that were modified in a later SSZ setting. Many massive chromite ores and zones of disseminated mineralization are present in the two massifs, and chromite ores have Cr#s 70-80, similar to those of the hosting dunite. The petrological features and metallogenic environment of the Dongbo and Purang massifs are very similar to those of the Luobusa peridotite massif, which hosts the largest chromite deposit in China. Thus, we propose that the Purang and Dongbo massifs are two potential locations for significant chromite deposits.

  13. 40 CFR 721.10370 - Phosphonic acid, p-octyl-, lanthanum (3+) salt (2:1).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Phosphonic acid, p-octyl-, lanthanum... New Uses for Specific Chemical Substances § 721.10370 Phosphonic acid, p-octyl-, lanthanum (3+) salt... substance identified as phosphinic acid, p-octyl-, lanthanum (3+) salt (2:1) (PMN P-10-99; CAS No....

  14. 40 CFR 721.10370 - Phosphonic acid, p-octyl-, lanthanum (3+) salt (2:1).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Phosphonic acid, p-octyl-, lanthanum... New Uses for Specific Chemical Substances § 721.10370 Phosphonic acid, p-octyl-, lanthanum (3+) salt... substance identified as phosphinic acid, p-octyl-, lanthanum (3+) salt (2:1) (PMN P-10-99; CAS No....

  15. 40 CFR 721.10370 - Phosphonic acid, p-octyl-, lanthanum (3+) salt (2:1).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Phosphonic acid, p-octyl-, lanthanum... New Uses for Specific Chemical Substances § 721.10370 Phosphonic acid, p-octyl-, lanthanum (3+) salt... substance identified as phosphinic acid, p-octyl-, lanthanum (3+) salt (2:1) (PMN P-10-99; CAS No....

  16. Tuning oxygen vacancy photoluminescence in monoclinic Y2WO6 by selectively occupying yttrium sites using lanthanum

    PubMed Central

    Ding, Bangfu; Han, Chao; Zheng, Lirong; Zhang, Junying; Wang, Rongming; Tang, Zilong

    2015-01-01

    The effect of isovalent lanthanum (La) doping on the monoclinic Y2WO6 photoluminescence was studied. Introducing the non-activated La3+ into Y2WO6 brings new excitation bands from violet to visible regions and strong near-infrared emission, while the bands position and intensity depend on the doping concentration. It is interesting to find that doping La3+ into Y2WO6 promotes the oxygen vacancy formation according to the first-principle calculation, Raman spectrum, and synchrotron radiation analysis. Through the Rietveld refinement and X-ray photoelectron spectroscopy results, La3+ is found to mainly occupy the Y2 (2f) site in low-concentration doped samples. With increasing doping concentration, the La3+ occupation number at the Y3 (4g) site increases faster than those at the Y1 (2e) and Y2 (2f) sites. When La3+ occupies different Y sites, the localized energy states caused by the oxygen vacancy pair change their position in the forbidden band, inducing the variation of the excitation and emission bands. This research proposes a feasible method to tune the oxygen vacancy emission, eliminating the challenge of precisely controlling the calcination atmosphere. PMID:25821078

  17. Methyl chloride production from methane over lanthanum-based catalysts.

    PubMed

    Podkolzin, Simon G; Stangland, Eric E; Jones, Mark E; Peringer, Elvira; Lercher, Johannes A

    2007-03-07

    The mechanism of selective production of methyl chloride by a reaction of methane, hydrogen chloride, and oxygen over lanthanum-based catalysts was studied. The results suggest that methane activation proceeds through oxidation-reduction reactions on the surface of catalysts with an irreducible metal-lanthanum, which is significantly different from known mechanisms for oxidative chlorination. Activity and spectroscopic measurements show that lanthanum oxychloride (LaOCl), lanthanum trichloride (LaCl3), and lanthanum phases with an intermediate extent of chlorination are all active for this reaction. The catalyst is stable with no noticeable deactivation after three weeks of testing. Kinetic measurements suggest that methane activation proceeds on the surface of the catalyst. Flow and pulse experiments indicate that the presence of hydrogen chloride is not required for activity, and its role appears to be limited to maintaining the extent of catalyst chlorination. In contrast, the presence of gas-phase oxygen is essential for catalytic activity. Density-functional theory calculations suggest that oxygen can activate surface chlorine species by adsorbing dissociatively and forming OCl surface species, which can serve as an active site for methane activation. The proposed mechanism, thus, involves changing of the formal oxidation state of surface chlorine from -1 to +1 without any changes in the oxidation state of the underlying metal.

  18. Phosphate adsorption on lanthanum loaded biochar.

    PubMed

    Wang, Zhanghong; Shen, Dekui; Shen, Fei; Li, Tianyu

    2016-05-01

    To attain a low-cost and high-efficient phosphate adsorbent, lanthanum (La) loaded biochar (La-BC) prepared by a chemical precipitation method was developed. La-BC and its pristine biochar (CK-BC) were comparatively characterized using zeta potential, BET surface area, scanning electron microscopy/energy dispersive spectrometer (SEM-EDS), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FT-IR). The adsorption ability and the mechanisms during adsorption process for the La-BC samples were also investigated. La loaded on the surface of biochar can be termed as La-composites (such as LaOOH, LaONO3 and La(OH)3), leading to the decrease of negative charge and surface area of biochar. La-BC exhibited the high adsorption capacity to phosphate compared to CK-BC. Adsorption isotherm and adsorption kinetic studies showed that the Langmuir isotherm and second order model could well describe the adsorption process of La-BC, indicating that the adsorption was dominated by a homogeneous and chemical process. The calculated maximum adsorption capacity was as high as 46.37 mg g(-1) (computed in P). Thermodynamic analysis revealed that the adsorption was spontaneous and endothermic. SEM, XRD, XPS and FT-IR analysis suggested that the multi-adsorption mechanisms including precipitation, ligand exchange and complexation interactions can be evidenced during the phosphate adsorption process by La-composites in La-BC.

  19. Toward laser cooling of negative lanthanum

    NASA Astrophysics Data System (ADS)

    Jordan, Elena; Cerchiari, Giovanni; Erlewein, Stefan; Kellerbauer, Alban; UNIC Team

    2016-05-01

    Anion laser cooling holds the potential to allow the production of ultracold ensembles of any negatively charged species by sympathetic cooling. It is a promising technique for cooling of antiprotons to a few mK and could clear the way for precision measurements on cold antihydrogen. Laser cooling of negative ions has never been achieved, since most species have no bound-bound electric dipole transitions. Negative lanthanum (La-) is one of the few anions with multiple electric dipole transitions. The bound-bound transition from the 3F2e ground state to the 3D1o excited state in La- has been proposed theoretically as a candidate for laser cooling. The potential laser cooling transition was identified using laser photodetachment spectroscopy and its excitation energy was measured. We have studied the aforementioned transition in a beam of La anions by high-resolution laser photodetachment spectroscopy. Seven of the nine expected hyperfine structure transitions have been resolved and the transition cross sections have been estimated from experimental observations. It was found that presently La- is the most promising candidate among the atomic anions. We plan to demonstrate the first direct laser cooling of negative ions in a linear radio frequency trap. We gratefully acknowledge support from the European Research Council (ERC).

  20. Spectroscopic characterization of chromite from the Moa-Baracoa Ophiolitic Massif, Cuba.

    PubMed

    Reddy, B Jagannadha; Frost, Ray L

    2005-06-01

    The Cuban chromites with a spinel structure, FeCr2O4 have been studied using optical absorption and EPR spectroscopy. The spectral features in the electronic spectra are used to map the octahedral and tetrahedral co-ordinated cations. Bands due Cr3+ and Fe3+ ions could be distinguished from UV-vis spectrum. Chromite spectrum shows two spin allowed bands at 17,390 and 23,810 cm(-1) due to Cr3+ in octahedral field and they are assigned to 4A2g(F) --> 4T2g(F) and 4A2g(F) --> 4T1g(F) transitions. This is in conformity with the broad resonance of Cr3+ observed from EPR spectrum at g = 1.903 and a weak signal at g = 3.861 confirms Fe3+ impurity in the mineral. Bands of Fe3+ ion in the optical spectrum at 13,700, 18,870 and 28,570 cm(-1) are attributed to 6A1g(S) --> 4T1g(G), 6A1g(S) --> 4T2g(G) and 6A1g(S) --> 4T2g(P) transitions, respectively. Near-IR reflectance spectroscopy has been used effectively to show intense absorption bands caused by electronic spin allowed d-d transitions of Fe2+ in tetrahedral symmetry, in the region 5000-4000 cm(-1). The high frequency region (7500-6500 cm(-1)) is attributed to the overtones of hydroxyl stretching modes. Correlation between Raman spectral features and mineral chemistry are used to interpret the Raman data. The Raman spectrum of chromite shows three bands in the CrO stretching region at 730, 560 and 445 cm(-1). The most intense peak at 730 cm(-1) is identified as symmetric stretching vibrational mode, A1g(nu1) and the other two minor peaks at 560 and 445 cm(-1) are assigned to F2g(nu4) and E(g)(nu2) modes, respectively. Cation substitution in chromite results various changes both in Raman and IR spectra. In the low-wavenumber region of Raman spectrum a significant band at 250 cm(-1) with a component at 218 cm(-1) is attributed F2g(nu3) mode. The minor peaks at 195, 175, 160 cm(-1) might be due to E(g) and F2g symmetries. Broadening of the peak of A1g mode and shifting of the peak to higher wavenumber observed as a result of

  1. Spectroscopic characterization of chromite from the Moa-Baracoa Ophiolitic Massif, Cuba

    NASA Astrophysics Data System (ADS)

    Reddy, B. Jagannadha; Frost, Ray L.

    2005-06-01

    The Cuban chromites with a spinel structure, FeCr 2O 4 have been studied using optical absorption and EPR spectroscopy. The spectral features in the electronic spectra are used to map the octahedral and tetrahedral co-ordinated cations. Bands due Cr 3+ and Fe 3+ ions could be distinguished from UV-vis spectrum. Chromite spectrum shows two spin allowed bands at 17390 and 23810 cm -1 due to Cr 3+ in octahedral field and they are assigned to 4A 2g(F) → 4T 2g(F) and 4A 2g(F) → 4T 1g(F) transitions. This is in conformity with the broad resonance of Cr 3+ observed from EPR spectrum at g = 1.903 and a weak signal at g = 3.861 confirms Fe 3+ impurity in the mineral. Bands of Fe 3+ ion in the optical spectrum at 13700, 18870 and 28570 cm -1 are attributed to 6A 1g(S) → 4T 1g(G), 6A 1g(S) → 4T 2g(G) and 6A 1g(S) → 4T 2g(P) transitions, respectively. Near-IR reflectance spectroscopy has been used effectively to show intense absorption bands caused by electronic spin allowed d -d transitions of Fe 2+ in tetrahedral symmetry, in the region 5000-4000 cm -1. The high frequency region (7500-6500 cm -1) is attributed to the overtones of hydroxyl stretching modes. Correlation between Raman spectral features and mineral chemistry are used to interpret the Raman data. The Raman spectrum of chromite shows three bands in the CrO stretching region at 730, 560 and 445 cm -1. The most intense peak at 730 cm -1 is identified as symmetric stretching vibrational mode, A 1g(ν 1) and the other two minor peaks at 560 and 445 cm -1 are assigned to F 2g(ν 4) and E g(ν 2) modes, respectively. Cation substitution in chromite results various changes both in Raman and IR spectra. In the low-wavenumber region of Raman spectrum a significant band at 250 cm -1 with a component at 218 cm -1 is attributed F 2g(ν 3) mode. The minor peaks at 195, 175, 160 cm -1 might be due to E g and F 2g symmetries. Broadening of the peak of A 1g mode and shifting of the peak to higher wavenumber observed as

  2. Chromite-rich mafic silicate chondrules in ordinary chondrites: Formation by impact melting

    NASA Technical Reports Server (NTRS)

    Krot, Alexander N.; Rubin, Alan E.

    1993-01-01

    Chromium-rich chondrules constitute less than 0.1 percent of all ordinary chondrite (OC) chondrules and comprise three groups: chromian-spinel chondrules, chromian-spinel inclusions, and chromite-rich mafic silicate (CRMS) chondrules. Chromian-spinel chondrules (typically 100-300 microns in apparent diameter) exhibit granular, porphyritic and unusual textures and occur mainly in H chondrites. Their morphologies are distinct from the irregularly shaped chromian-spinel inclusions of similar mineralogy. Chromian-spinel chondrules and inclusions consist of grains of chromian-spinel embedded in plagioclase (Pl) or mesostasis of Pl composition. Many also contain accessory ilmenite (Ilm), high-Ca pyroxene (Px), merrillite (Mer), and rare olivine (Ol); some exhibit concentric mineral and chemical zoning. CRMS chondrules (300-1100 microns in apparent diameter) are generally larger than chromian-spinel chondrules and occur in all metamorphosed OC groups. Most CRMS chondrules are nearly spherical although a few are ellipsoidal with a/b aspect ratios ranging up to 1.7. Textures include cryptocrystalline, granular, radial, barred, and porphyritic varieties; some contain apparently relict grains. The chondrules consist of chromite (Chr), Ol and Pl, along with accessory Mer, troilite (Tr), metallic Fe-Ni (Met), Px and Ilm. The mesostasis in CRMS chondrules is nearly opaque in transmitted light; thus, they can be easily recognized in the optical microscope. Based on the similarity of mineralogy and chemistry between CRMS chondrules of different textures (opaque chromite-rich mesostasis, skeletal morphology of Ol grains, similar bulk compositions) we suggest that these chondrules form a genetically related population.

  3. Nanostructured Lanthanum Halides and CeBr3 for Nuclear Radiation and Detection

    SciTech Connect

    Paul Guss, Sanjoy Mukhopadhyay, Ron Guise, Ding Yuan

    2010-06-09

    Scintillator materials are used to detect, and in some cases identify, gamma rays. Higher performance scintillators are expensive, hard to manufacture, fragile, and sometimes require liquid nitrogen or cooling engines. But whereas lower-quality scintillators are cheap, easy to manufacture, and more rugged, their performance is lower. At issue: can the desirable qualities of high-and low-performance scintillators be combined to achieve better performance at lower cost? Preliminary experiments show that a LaF{sub 3}:Ce oleic acid-based nanocomposite exhibits a photopeak when exposed to {sup 137}Cs source gamma-radiation. The chemical synthesis of the cerium-doped lanthanum halide nanoparticles are scalable and large quantities of material can be produced at a time, unlike typical crystal growth processes such as the Bridgeman process. Using a polymer composite (Figure 1), produced by LANL, initial measurements of the unloaded and 8% LaF{sub 3}:Ce-loaded sample have been made using {sup 137}Cs sources. Figure 2 shows an energy spectrum acquired for CeF{sub 3}. The lighter plot is the measured polymer-only spectrum and the black plot is the spectrum from the nanocomposite scintillator. As the development of this material continues, the energy resolution is expected to improve and the photopeak-to-Compton ratio will become greater at higher loadings. These measurements show the expected Compton edge in the polymer-only sample, and the Compton edge and photo-peak expected in the nanophosphor composites that LANL has produced. Using a porous VYCORR with CdSe/ZnS core shell quantum dots, Letant has demonstrated that he has obtained signatures of the 241Am photopeak with energy resolution as good at NaI (Figure 3). We begin with the fact that CeBr{sub 3} crystals do not have a self-activity component as strong as the lanthanum halides. The radioactive 0.090% {sup 138}La component of lanthanum leads to significant self-activity, which will be a problem for very large

  4. Electro-optical polycrystalline barium lanthanum titanium niobate

    SciTech Connect

    Mehrotra, A.K.

    1991-02-19

    This patent describes a transparent electro-optic article. It comprises: of a barium lanthanum titanium niobate wherein substantially all grains are of a grain size between about 2 and about 20 micron, the article has a pore volume of less than about 1 percent, and the article has a grain size of between about 2 and about 20 microns. This patent also describes a method of forming transparent electro-optical barium lanthanum titanium niobate. It comprises: providing particles of barium carbonate, lanthanum oxide, titanium oxide, and niobium oxide, calcining the particles, sintering the calcined particles at a temperature of between about 1200{degrees} C and 1300{degrees} C. and a vacuum of between about 10{sup {minus}3} and 10{sup {minus}4} torr while under pressure to form a sintered mass, cooling the sintered mass, slicing the mass to form wafers, heating the wafers in an oxidizing atmosphere.

  5. Calcium and lanthanum solid base catalysts for transesterification

    SciTech Connect

    Ng, K. Y. Simon; Yan, Shuli; Salley, Steven O.

    2015-07-28

    In one aspect, a heterogeneous catalyst comprises calcium hydroxide and lanthanum hydroxide, wherein the catalyst has a specific surface area of more than about 10 m.sup.2/g. In another aspect, a heterogeneous catalyst comprises a calcium compound and a lanthanum compound, wherein the catalyst has a specific surface area of more than about 10 m.sup.2/g, and a total basicity of about 13.6 mmol/g. In further another aspect, a heterogeneous catalyst comprises calcium oxide and lanthanum oxide, wherein the catalyst has a specific surface area of more than about 10 m.sup.2/g. In still another aspect, a process for preparing a catalyst comprises introducing a base precipitant, a neutral precipitant, and an acid precipitant to a solution comprising a first metal ion and a second metal ion to form a precipitate. The process further comprises calcining the precipitate to provide the catalyst.

  6. Remediation of chromite ore processing residue by pyrolysis process with sewage sludge.

    PubMed

    Zhang, Dalei; Kong, Hainan; Wu, Deyi; He, Shengbing; Hu, Zhanbo; Hu, Xiaofang

    2009-06-01

    The present work developed a novel technique to treat chromite ore processing residue (COPR). The process involved mixing the COPR with sewage sludge followed by pyrolysis. The gaseous organic fraction generated during pyrolysis of sludge was beneficial to Cr(VI) reduction. Process variables, such as the amount of sludge added to COPR (sludge-to-COPR (S/C) ratio), heating temperature, reaction time and particle size, were systematically varied, and their influences on the Cr(VI) reduction in COPR were investigated. Cr(VI) content had decreased greatly, from 3384 mg kg(-1) for untreated COPR to less than 30 mg kg(-1) for COPR treated at 600 degrees C.

  7. Synthesis of lanthanum aluminate by reverse chemical precipitation using pseudoboehmite as alumina precursor.

    PubMed

    Wilson, Hernández Muñoz; Juan, Serrato Rodríguez; Juan, Muñoz Saldaña; Juan, Zárate Medina

    2016-11-01

    Lanthanum aluminate was synthesized by using reverse precipitation. A lanthanum nitrate salt in solution allowed the precipitation of lanthanum hydroxide onto the surface of the pseudoboehmite particles. Pseudoboehmite was previously synthesized out of aluminum sulfate which after characterization presents a poor crystallized structure. A Perovskite-type lanthanum aluminate was obtained at different temperature and calcination time. When calcination was set up to 1500°C to 3°C/min pure, high crystallinity and highly agglomerated lanthanum aluminate is obtained, relative density of 94% was reached.

  8. SEPARATION OF PLUTONIUM FROM LANTHANUM BY CHELATION-EXTRACTION

    DOEpatents

    James, R.A.; Thompson, S.G.

    1958-12-01

    Plutonium can be separated from a mixture of plutonlum and lanthanum in which the lanthanum to plutonium molal ratio ls at least five by adding the ammonium salt of N-nitrosoarylhydroxylamine to an aqueous solution having a pH between about 3 and 0.2 and containing the plutonium in a valence state of at least +3, to form a plutonium chelate compound of N-nitrosoarylhydroxylamine. The plutonium chelate compound may be recovered from the solution by extracting with an immiscible organic solvent such as chloroform.

  9. Enhancement of Superconductivity of Lanthanum and Yttrium Sesquicarbide

    DOEpatents

    Krupka, M. C.; Giorgi, A. L.; Krikorian, N. H.; Szklarz, E. G.

    1972-06-22

    A method of enhancing the superconductivity of body-centered cubic lanthanum and yttrium sesquicarbide through formation of the sesquicarbides from ternary alloys of novel composition (N/sub x/M/sub 1-x/)C/sub z/, where N is yttrium or lanthanum, M is thorium, any of the Group IV and VI transition metals, or gold, germanium or silicon, and z is approximately 1.2 to 1.6. These ternary sesquicarbides have superconducting transition temperatures as high as 17.0/sup 0/K.

  10. Enhancement of superconductivity of lanthanum and yttrium sesquicarbide

    DOEpatents

    Krupka, M.C.; Giorgi, A.L.; Krikorian, N.H.; Szklarz, E.G.

    1971-06-22

    A method of enhancing the superconductivity of body-centered cubic lanthanum and yttrium sesquicarbide through formation of the sesquicarbides from ternary alloys of novel composition (N/sub x/M/sub 1-x/)C/sub z/, where N is yttrium or lanthanum, M is thorium, any of the Group IV and VI transition metals, or gold, germanium or silicon, and z is approximately 1.2 to 1.6. These ternary sesquicarbides have superconducting transition temperatures as high as 17.0/sup 0/K.

  11. Volatile products from the interaction of KCl(g) with Cr2O3 and LaCrO3 in oxidizing environments

    NASA Technical Reports Server (NTRS)

    Kohl, F. J.; Miller, R. A.; Stearns, C. A.; Fryburg, G. C.; Dillard, J. G.

    1977-01-01

    Cooled target collection techniques and high pressure mass spectrometric sampling were used to measure the relative rates of oxidative vaporization and to identify the volatile products emanating from samples of chromia and Mg-doped lanthanum chromite. The materials were exposed to partial pressures of KCl with and without H2O in one atmosphere of slowly flowing oxygen at elevated temperatures. Chromia and fresh samples of lanthanum chromite exhibited enhanced rates of oxidative vaporization upon exposure to these reactants. Mass spectrometric identification showed that the enhancements resulted from the heterogeneous formation of complex molecules of the type KCl sub 1,2,3 CrO3 and KOH sub l,2 CrO3. Lanthanum chromite that had undergone prolonged oxidative vaporization exhibited no enhanced oxidation upon exposure to the reactants.

  12. Phase dependent structural and electronic properties of Lanthanum Orthophosphate (LaPO4)

    NASA Astrophysics Data System (ADS)

    Neupane, Mahesh; Garrett, Gregory; Rudin, Sergey; Andzelm, Jan

    Lanthanum orthophosphate (LaPO4) belongs to the family of rare-earth (RE) orthophosphates. The La-ion lacks valence 4f-electron, so for it to exhibit f-electron dependent physics, it must be doped with additional RE elements. In the bulk form, LaPO4 exist in both a stable monoclinic and a metastable hexagonal phase, which both possess indirect energy transition characteristics. Though the overall optoelectronic properties of the RE-doped LaPO4 depend on the accuracy of the observed bulk energy gap, the reported experimental and theoretical energy gaps varies between ~81,2 and ~53 eV, respectively. Through this theoretical study, we attempt to establish a correlation between electronic properties of bulk LaPO4 and various levels of first principle theories. Compared to experimental data, the PBE0 functional over-predicts energy gaps and the energy differences between the indirect-to-direct transition energies by 25%. The HSE06 gives a good description of electronic properties and predicts the energy gaps to be 7.68 (monoclinic) and 7.29 eV (hexagonal). Analysis on the structural stability also reveals that the total energy difference between the two phases is 6meV, consistent with the experimentally observed instantaneous pressure and temperature dependent phase transition.

  13. X-Band Microwave Reflection Properties of Samarium/Bismuth-Substituted Barium Lanthanum Titanate Ceramics

    NASA Astrophysics Data System (ADS)

    Bahel, Shalini; Pubby, Kunal; Narang, Sukhleen Bindra

    2017-01-01

    Samarium/bismuth-substituted barium lanthanum titanate ceramics with chemical composition Ba4 (La_{1 - y - z} Smy Biz )_{9.33} Ti_{18} O_{54} (y = 0.5, 0.7; z = 0.05, 0.10, 0.15), intended as microwave reflecting materials, have been investigated in microwave X-band (8.2 GHz to 12.4 GHz) and the effect of substitution on their dielectric properties, i.e., dielectric constant and dielectric loss tangent, has been studied by vector network analyzer. Dielectric analysis showed that the dielectric constant increased with increasing samarium as well as bismuth content. Dielectric relaxation was observed for all samples in the scanned frequency range. Microwave reflection and transmission analysis of ceramic pellets of thickness 4 mm was carried out using two methods, i.e., open- and short-circuit approach, both indicating very high values of reflected power and very low values of transmitted power for all the doped materials in comparison with the base composition. The doped compositions are therefore potential microwave shielding materials for use in anechoic chambers, microwave laboratories, and radar equipment. Double-layer reflectors are also proposed, having better reflection properties (˜99% reflection) compared with single-layer reflectors.

  14. Tuning the architecture and properties of microstructured yttrium tungstate oxide hydroxide and lanthanum tungstate.

    PubMed

    Kaczmarek, Anna M; Liu, Ying-Ya; Van der Voort, Pascal; Van Deun, Rik

    2013-04-21

    In this paper, various microstructures of yttrium and lanthanum tungstates were synthesized under hydrothermal conditions, at pH 5, in a ligand-free environment, and in the presence of a dioctyl sodium sulfosuccinate (DSS) surfactant. It was observed that the shape of the nanobuilding blocks, and therefore the architecture of the microstructures, could be tuned by controlling the reaction conditions, such as the source of the rare earth, the amount of a surfactant and the reaction time. X-ray powder diffraction (XRD), elemental analysis, scanning electron microscopy (SEM), and N2 adsorption were employed to characterize the obtained products. The photoluminescent properties of Eu(3+) and Dy(3+) doped tungstate materials were investigated. Luminescence measurements showed an efficient charge transfer from the WO4(2-) groups to Eu(3+) and Dy(3+) ions. It was found that under UV excitation the Dy(3+) doped Y(WO3)2(OH)3 and La2(WO4)3 precursors exhibit white emission.

  15. X-Band Microwave Reflection Properties of Samarium/Bismuth-Substituted Barium Lanthanum Titanate Ceramics

    NASA Astrophysics Data System (ADS)

    Bahel, Shalini; Pubby, Kunal; Narang, Sukhleen Bindra

    2017-03-01

    Samarium/bismuth-substituted barium lanthanum titanate ceramics with chemical composition Ba4 (La_{1 - y - z} Smy Biz )_{9.33} Ti_{18} O_{54} ( y = 0.5, 0.7; z = 0.05, 0.10, 0.15), intended as microwave reflecting materials, have been investigated in microwave X-band (8.2 GHz to 12.4 GHz) and the effect of substitution on their dielectric properties, i.e., dielectric constant and dielectric loss tangent, has been studied by vector network analyzer. Dielectric analysis showed that the dielectric constant increased with increasing samarium as well as bismuth content. Dielectric relaxation was observed for all samples in the scanned frequency range. Microwave reflection and transmission analysis of ceramic pellets of thickness 4 mm was carried out using two methods, i.e., open- and short-circuit approach, both indicating very high values of reflected power and very low values of transmitted power for all the doped materials in comparison with the base composition. The doped compositions are therefore potential microwave shielding materials for use in anechoic chambers, microwave laboratories, and radar equipment. Double-layer reflectors are also proposed, having better reflection properties (˜99% reflection) compared with single-layer reflectors.

  16. Chemical and mineralogical characterization of chromite ore processing residue from two recent Indian disposal sites.

    PubMed

    Matern, Katrin; Kletti, Holger; Mansfeldt, Tim

    2016-07-01

    Chromite ore processing residue (COPR) is a hazardous waste. Nevertheless, deposition of COPR in uncontrolled surface landfills is still common practice in some countries. Whereas old (between at least 40 and 180 years) COPR from the temperate zone has been intensively investigated, information on COPR in other regions is restricted. Relatively young (<25 years) COPR samples obtained from two abandoned landfill sites in India were investigated by a modified total microwave digestion method, X-ray powder diffraction (XRPD), and scanning electron microscopy (SEM) in order to determine their chemical and mineralogical nature. By the use of microwave digestion with acid mixtures of HNO3, H3PO4, and HBF4 (5:3:2 vol), COPR was completely dissolved and element contents similar to those obtained by X-ray fluorescence were found. Total Cr contents of the two COPR accounted for 81 and 74 g kg(-1), of which 20 and 13% were present in the carcinogenic hexavalent form (CrVI). Apart from the common major mineral phases present in COPR reported earlier, a further Cr host mineral, grimaldiite [CrO(OH)], could be identified by XRPD and SEM. Additionally, well soluble Na2CrO4 was present. Improving the effectiveness of chromite ore processing and preventing the migration of Cr(VI) into water bodies are the main challenges when dealing with these COPR.

  17. Microbial leaching of chromite overburden from Sukinda mines, Orissa, India using Aspergillus niger

    NASA Astrophysics Data System (ADS)

    Biswas, Supratim; Samanta, Saikat; Dey, Rajib; Mukherjee, Siddhartha; Banerjee, Pataki C.

    2013-08-01

    Leaching of nickel and cobalt from two physical grades (S1, 125-190 μm, coarser and S3, 53-75 μm, finer) of chromite overburden was achieved by treating the overburden (2% pulp density) with 21-d culture filtrate of an Aspergillus niger strain grown in sucrose medium. Metal dissolution increases with ore roasting at 600°C and decreasing particle size due to the alteration of microstructural properties involving the conversion of goethite to hematite and the increase in surface area and porosity as evident from X-ray diffraction (XRD), thermogravimetry-differential thermal analysis (DT-TGA), and field emission scanning electron microscopy (FESEM). About 65% Ni and 59% Co were recovered from the roasted S3 ore employing bioleaching against 26.87% Ni and 31.3% Co using an equivalent amount of synthetic oxalic acid under identical conditions. The results suggest that other fungal metabolites in the culture filtrate played a positive role in the bioleaching process, making it an efficient green approach in Ni and Co recovery from lateritic chromite overburden.

  18. Discovery of cesium, lanthanum, praseodymium and promethium isotopes

    SciTech Connect

    May, E.; Thoennessen, M.

    2012-09-15

    Currently, forty-one cesium, thirty-five lanthanum, thirty-two praseodymium, and thirty-one promethium isotopes have been observed and the discovery of these isotopes is described here. For each isotope a brief synopsis of the first refereed publication, including the production and identification method, is presented.

  19. Petrogenesis of chromites from the Manipur ophiolite belt, NE India: evidence for a supra-subduction zone setting prior to Indo-Myanmar collision

    NASA Astrophysics Data System (ADS)

    Pal, Tapan; Bhattacharya, Anindya; Nagendran, G.; Yanthan, N. M.; Singh, R.; Raghumani, N.

    2014-10-01

    The Manipur ophiolite belt within the Western Ophiolite Belt of the Indo-Myanmar Ranges (IMR), consists of tectonised to massive serpentinised peridotite, dunite pods, chromitite pods/lenses, cumulates, dykes, volcanic rocks and pelagic sediments. Chromitite pods and lenses hosted in peridotitic mantle rocks show magmatic textures, post magmatic brecciation and ferritchromitisation. Electron microprobe analyses show two types of massive chromitite, with one group having high-Cr (Cr# 75-76), medium-Al (Al2O3 12.2-12.4 wt%) chromites (Sirohi-type) and the other group (Gamnom-type) having a wide range of compositions with generally lower Cr and higher Al (Cr# 65-71, Al2O3 15.7-19 wt%). Accessory chromites in peridotitic mantle rocks have consistently low Cr (Cr# 38-39) and high Al (Al2O3 34-35 wt%), whereas chromites in dunite pods have intermediate compositions (Cr# ~60; Al2O3 20.7-21.2 wt%). The chromite chemistry suggests moderate (20 %) partial melting of the tectonised mantle harzburgite. The estimated Al2O3melt, (FeO/MgO)melt and TiO2melt for the Sirohi-type chromites indicate boninitic parentage, whereas chromite compositions from the Gamnom area suggest mixed boninitic—island arc tholeiitic magmas. The compositions of magmatic chromites suggest that the Manipur ophiolite was formed in a supra-subduction zone (SSZ) setting.

  20. PGE distribution in the Chromite bearing mafic-ultramafic Kondapalli Layered Complex, Krishna district, Andhra Pradesh, India

    NASA Astrophysics Data System (ADS)

    Meshram, Tushar M.; Nannaware, Shraddha. B.; Nannaware, B.; Bhatacharjee, Shantanu; Waghmare, Minakshi. M.; Rajakumar, T.

    2015-09-01

    The Kondapalli Layered Complex (KLC) is a dismembered mafic-ultramafic layered intrusion, mainly composed of gabbroic and anorthositic rocks with subordinate ultramafics and chromitite. Chromitite occurs as lenses, pods, bands and disseminations. Platinum group of minerals (PGMs) occur as inclusions within chromite and silicates. The study indicates an inhomogeneous distribution of PGMs and distinct dominance of IPGEs over the PPGEs. The average ΣPGE content of chromite of KLC varies from 64 ppb to 576 ppb with Pt ranging from 5 to 495 ppb, Pd 5 to 191 ppb, Ir 3 to 106 ppb, Ru 3 to 376 ppb and Rh 3 to 135 ppb. The PGMs identified in the KLC indicate primary deposition of the IPGE, preceding chromite, indicating its orthomagmatic nature. Most of the PGM grains are usually below 10 μm. The identified PGMs are Laurite (RuS2), irarsite (Ir, As, S), iridosmine (Os, Ir), undetermined Os-Ir sulphide and Ru-Os-Ir-Zn alloys. Chromite also contains inclusions of pentlandite, millerite, chalcopyrite and pyrite. Study indicating that the KLC have orthomagmatic origin for PGE which are dominated by IPGE group and formed under surpa-subduction zone peridotite setting.

  1. Platinum-group element abundance and distribution in chromite deposits of the Acoje Block, Zambales Ophiolite Complex, Philippines

    USGS Publications Warehouse

    Bacuta, G.C.; Kay, R.W.; Gibbs, A.K.; Lipin, B.R.

    1990-01-01

    Platinum-group elements (PGE) occur in ore-grade concentration in some of the chromite deposits related to the ultramafic section of the Acoje Block of the Zambales Ophiolite Complex. The deposits are of three types: Type 1 - associated with cumulate peridotites at the base of the crust; Type 2 - in dunite pods from the top 1 km of mantle harzburgite; and Type 3 - like Type 2, but in deeper levels of the harzburgite. Most of the deposites have chromite compositions that are high in Cr with Cr/(Cr + Al) (expressed as chromium index, Cr#) > 0.6; high-Al (Cr# Pd, thought to be characteristic of PGE-barren deposits) and positive slope (Ir < Pd, characteristic of PGE-rich deposits). Iridium, Ru and Os commonly occur as micron-size laurite (sulfide) inclusions in unfractured chromite. Laurite and native Os are also found as inclusions in interstitial sulfides. Platinum and Pd occur as alloy inclusions (and possibly as solid solution) in interstitial Ni-Cu sulfides and as tellurobismuthides in serpentine and altered sulfides. Variability of PGE distribution may be explained by alteration, crystal fractionation or partial melting processes. Alteration and metamorphism were ruled out, because PGE contents do not correlate with degree of serpentinization or the abundance and type (hydroxyl versus non-hydroxyl) of silicate inclusions in chromite. Preliminary Os isotopic data do not support crustal contamination as a source of the PGEs in the Acoje deposits. The anomalous PGE concentrations in Type 1 high-Cr chromite deposits are attributed to two stages of enrichment: an early enrichment of their mantle source from previous melting events and a later stage of sulfide segregation accompanying chromite crystallization. High-Al chromite deposits which crystallized from basalts derived from relatively low degrees of melting owe their low PGE content to partitioning of PGEs in sulfides and alloys that remain in the mantle. High-Cr deposits crystallized from melts that were

  2. Phosphate-binding efficacy of crushed vs. chewed lanthanum carbonate in hemodialysis patients.

    PubMed

    How, Priscilla P; Anattiwong, Prathana; Mason, Darius L; Arruda, Jose A; Lau, Alan H

    2011-01-01

    Lanthanum carbonate, a chewable noncalcium-containing phosphorus (P) binder, is useful for treating secondary hyperparathyroidism in patients who have hypercalcemia and cannot swallow whole tablets. However, some patients cannot chew tablets or prefer to crush and mix them with food. This study was conducted to determine the P-binding efficacy of crushed lanthanum and compare it with chewed lanthanum in hemodialysis (HD) patients. After a 1-week washout period, 11 hemodialysis patients (7 men, 4 women) were randomized to receive, in a crossover fashion, lanthanum 1000 mg 3 times daily chewed with meals and lanthanum 1000 mg 3 times daily crushed into a fine powder, mixed with applesauce and taken with meals, for 4 weeks each. Serum P was measured at the end of each washout (baseline) and weekly during treatment. Changes in serum P from baseline for crushed lanthanum were compared with chewed lanthanum using paired sample t test. Administration of crushed lanthanum resulted in a significant reduction in serum P from baseline (P reduction [mg/dL] for crushed lanthanum in week 1: 2.1 ± 0.4, week 2: 1.7 ± 0.5, week 3: 1.7 ± 0.5, week 4: 1.7 ± 0.4, P<0.05). No statistically significant differences were observed in serum P reduction from baseline and serum P attained during treatment with crushed when compared with chewed lanthanum. Crushed lanthanum is effective in reducing serum P and have similar P-binding efficacy to chewed lanthanum. Crushing lanthanum and mixing it with food can thus be an option for patients who are unable to chew or swallow whole tablets.

  3. Structural Characterization of Methanol Substituted Lanthanum Halides

    PubMed Central

    Boyle, Timothy J.; Ottley, Leigh Anna M.; Alam, Todd M.; Rodriguez, Mark A.; Yang, Pin; Mcintyre, Sarah K.

    2010-01-01

    The first study into the alcohol solvation of lanthanum halide [LaX3] derivatives as a means to lower the processing temperature for the production of the LaBr3 scintillators was undertaken using methanol (MeOH). Initially the de-hydration of {[La(µ-Br)(H2O)7](Br)2}2 (1) was investigated through the simple room temperature dissolution of 1 in MeOH. The mixed solvate monomeric [La(H2O)7(MeOH)2](Br)3 (2) compound was isolated where the La metal center retains its original 9-coordination through the binding of two additional MeOH solvents but necessitates the transfer of the innersphere Br to the outersphere. In an attempt to in situ dry the reaction mixture of 1 in MeOH over CaH2, crystals of [Ca(MeOH)6](Br)2 (3) were isolated. Compound 1 dissolved in MeOH at reflux temperatures led to the isolation of an unusual arrangement identified as the salt derivative {[LaBr2.75•5.25(MeOH)]+0.25 [LaBr3.25•4.75(MeOH)]−0.25} (4). The fully substituted species was ultimately isolated through the dissolution of dried LaBr3 in MeOH forming the 8-coordinated [LaBr3(MeOH)5] (5) complex. It was determined that the concentration of the crystallization solution directed the structure isolated (4 concentrated; 5 dilute) The other LaX3 derivatives were isolated as [(MeOH)4(Cl)2La(µ-Cl)]2 (6) and [La(MeOH)9](I)3•MeOH (7). Beryllium Dome XRD analysis indicated that the bulk material for 5 appear to have multiple solvated species, 6 is consistent with the single crystal, and 7 was too broad to elucidate structural aspects. Multinuclear NMR (139La) indicated that these compounds do not retain their structure in MeOD. TGA/DTA data revealed that the de-solvation temperatures of the MeOH derivatives 4 – 6 were slightly higher in comparison to their hydrated counterparts. PMID:20514349

  4. Oriented chromite-diopside symplectic inclusions in olivine from lunar regolith delivered by "Luna-24" mission

    NASA Astrophysics Data System (ADS)

    Khisina, N. R.; Wirth, R.; Abart, R.; Rhede, D.; Heinrich, W.

    2013-03-01

    Calcium-chromium rich lamellae in olivine grain No. 1611 from the Luna-24 regolith were studied with FEG-EMPA and TEM. The lamellae consist of a worm-like intergrowth of FeCr2O4 chromite (Chr) and CaMgSi2O6 diopside (Di), with a Chr:Di modal proportion of 1:3. The linear extension of the lamellae and crystallographic orientation relationships among the symplectite phases and the olivine suggest that the lamellae nucleated at deformation defects in the olivine host. Calcium depletion haloes surrounding the lamellae amount to about 75 μm and indicate that the chromite + diopside lamellae were formed by segregation of calcium and chromium from the host olivine into the lamellae without addition of calcium and/or chromium from outside the olivine. The segregation of calcium and chromium and, consequently, the growth of the symplectic lamellae were diffusion-controlled. The segregation of a calcium-chromium component from the host olivine was associated with oxidation of divalent to trivalent chromium. Oxidation was facilitated by dehydrogenation, which was driven by decompression and/or a change in redox potential. Hydrogen point defects in the original olivine with H+ substituting for divalent cations on the M-sites provided the necessary electron acceptors for the oxidation of chromium and after electron transfer left olivine as molecular H2. The internal microstructure of the lamellae suggests that exsolution of the calcium-chromium rich lamellae from the host olivine and formation of the chromite-diopside symplectic intergrowth occurred simultaneously. The time scale derived from diffusion modeling of the calcium depletion haloes around the lamellae indicates a thermal event on the order of several months to several hundred years at most. Symplectic inclusions found in olivine from lunar, martian and terrestrial rocks are similar with respect to their shape, crystallographic orientation relationships, and internal microstructure of the spinel

  5. Mont Albert to Buck Mountain: Provenance of Appalachian Ophiolite Chromites Using Osmium Isotopes

    NASA Astrophysics Data System (ADS)

    Minarik, W. G.; Gale, A.; Booker, C.

    2003-12-01

    Osmium 187Os/188Os isotopic ratios have been determined for chrome-rich spinels from a suite of Appalachian ophiolites thought to represent Iapetus margin mantle formed and emplaced during the Ordovician. Because Re is incompatible during mantle melting while Os is compatible, non-radiogenic initial 187Os/188Os can constrain the average source and the timing of melt extraction, especially as Os is concentrated in chromite. Radiogenic ratios indicate contamination from aged sources with high Re/Os, such as mafic or continental crust. In rocks where spinel is the only remaining primary mineral, these properties can constrain the tectonic environment of formation as well as active-margin Os transport. There is little correction for 187Os in-growth since the Ordovician due to very low sample Re. Each ultramafic unit (from Mont Albert on the Gaspé Peninsula of Québec down to the Blue Ridge of North Carolina) forms a unique cluster of 187Os/188Os ratios, spanning 1 to 3%, but the whole range is about 10%. This corresponds to a range of initial γ Os of -1 to +9, where γ Os is the percent deviation from a chondritic source at the age of formation (roughly 500 Ma). Within ophiolites where detailed mapping and other geochemical information are available, there is a correlation between mantle-like Os and tholeiitic basalts; radiogenic Os and boninites (Thetford Mines). Continental arc-related mantle chromites (Baltimore Mafic Complex; γ Os +4 to +7) are the most radiogenic. The least radiogenic are chromites from the Staten Island serpentinite and Mont Albert (γ Os -1 and 0, respectively), either indicating formation from a previously depleted source or that they predate the other Taconic ophiolites. The restricted range of each ophiolite, compared to the whole of the data set, allow provenance links to be made between isolated bodies. For example, the Buck Creek, NC ultramafic complex, which has undergone granulite facies metamorphism, (Tenthorey et al., 1996) has a

  6. Radiotracer study of the preparation of high-purity lanthanum fluoride

    SciTech Connect

    Ewing, K.J.; Jaganathan, J.; Peitersen, L.; Aggarwal, I.D. ); Sommers, J.A.; Fahey, J.V. )

    1992-06-01

    This paper reports that the behavior of the impurities iron, cobalt, yttrium, and cerium is determined via radiotracer techniques for the preparation of high-purity lanthanum fluoride. The behavior of nickel and copper during the coprecipitation of a lanthanum nitrate solution is determined by graphite furnace atomic absorption spectrometric (GFAAS) analysis. There is no commercially available radiotracer for neodymium, a key impurity associated with absorption losses in fluoride glasses. However, the chemical behavior of neodymium and that of yttrium are very similar and, therefore, it is reasonable to assume that the behavior of yttrium throughout the processing is indicative of the behavior of neodymium. The concentrations of impurities in lanthanum nitrate, carbonate, and fluoride are estimated using the radiotracer and GFAAS data for each processing step. Results indicate that while high-purity lanthanum carbonate can be prepared, any impurities present in the lanthanum carbonate will be carried quantitatively into lanthanum fluoride upon hydrofluorination.

  7. Methanol synthesis using a catalyst combination of alkali or alkaline earth salts and reduced copper chromite

    DOEpatents

    Tierney, J.W.; Wender, I.; Palekar, V.M.

    1995-01-24

    The present invention relates to a novel route for the synthesis of methanol, and more specifically to the production of methanol by contacting synthesis gas under relatively mild conditions in a slurry phase with a catalyst combination comprising reduced copper chromite and basic alkali salts or alkaline earth salts. The present invention allows the synthesis of methanol to occur in the temperature range of approximately 100--160 C and the pressure range of 40--65 atm. The process produces methanol with up to 90% syngas conversion per pass and up to 95% methanol selectivity. The only major by-product is a small amount of easily separated methyl formate. Very small amounts of water, carbon dioxide and dimethyl ether are also produced. The present catalyst combination also is capable of tolerating fluctuations in the H[sub 2]/CO ratio without major deleterious effect on the reaction rate. Furthermore, carbon dioxide and water are also tolerated without substantial catalyst deactivation.

  8. Methanol synthesis using a catalyst combination of alkali or alkaline earth salts and reduced copper chromite

    DOEpatents

    Tierney, John W.; Wender, Irving; Palekar, Vishwesh M.

    1995-01-01

    The present invention relates to a novel route for the synthesis of methanol, and more specifically to the production of methanol by contacting synthesis gas under relatively mild conditions in a slurry phase with a catalyst combination comprising reduced copper chromite and basic alkali salts or alkaline earth salts. The present invention allows the synthesis of methanol to occur in the temperature range of approximately 100.degree.-160.degree. C. and the pressure range of 40-65 atm. The process produces methanol with up to 90% syngas conversion per pass and up to 95% methanol selectivity. The only major by-product is a small amount of easily separated methyl formate. Very small amounts of water, carbon dioxide and dimethyl ether are also produced. The present catalyst combination also is capable of tolerating fluctuations in the H.sub.2 /CO ratio without major deleterious effect on the reaction rate. Furthermore, carbon dioxide and water are also tolerated without substantial catalyst deactivation.

  9. Treatment of chromite ore processing residue by pyrolysis with rice straw.

    PubMed

    Zhang, Dalei; He, Shengbing; Dai, Luwei; Hu, Xiaofang; Wu, Deyi; Peng, Kangjin; Bu, Guanhuan; Pang, Hao; Kong, Hainan

    2009-11-01

    Chromite Ore Processing Residue (COPR) is the byproduct of chromate production process, which contains a large amounts of Cr(VI). The present work developed a new technique to treat COPR, and the process involved mixing the COPR with rice straw followed by pyrolysis. It was found that the gaseous organic fraction generated during pyrolysis of straw was beneficial to Cr(VI) reduction. In the study, process variables, such as the amount of straw added to COPR, heating temperature and particle size, were systematically varied, and their influences on the Cr(VI) reduction in COPR were all investigated. After pyrolysis, Cr(VI) decreased greatly, from 3400 for untreated COPR to less than 30 mg kg(-1) for treated COPR at 600 degrees C.

  10. Analysis of chromite by cation-exchange using ethylenediaminetetra-acetic acid.

    PubMed

    Jawaid, M; Ingman, F

    1975-12-01

    A method for the separation and determination of five major elements in chromite ore (and chrome-bearing refractories), based on complexation of the metals with EDTA is described. After removal of silica, the cations are separated into two groups by passing the solution through a cation-exchange resin (Dowex 50W-X8, in Na-form) in the presence of an excess of the complexing agent. The optimum conditions for the separation are discussed on the basis of exchange constants that were either known or determined. The first group contains Cr and Fe, which emerge in the filtrate at pH between 1.5 and 2.1, whereas A1, Mg and Ca, which are adsorbed on the resin, form another group. Complexometric titrations are used for the subsequent determination of the cations in each group. The method is simpler and more rapid and accurate for routine analysis than the current methods.

  11. The structural evolution of dunite and chromite ore from the Kharcheruz Massif, the Polar Urals

    NASA Astrophysics Data System (ADS)

    Chernyshov, A. I.; Yurichev, A. N.

    2016-03-01

    The Kharcheruz block of the Syumkeu ultramafic massif is a southern fragment of the Khadata ophiolitic belt, which closes the ophiolites of the Polar Urals in the north. The block, striking in the latitudinal direction, is sheetlike in shape and primarily composed of dunite with nearly latitudinal zones of chromite mineralization. The dunites are subject to ductile deformation various in intensity, and this variability is displayed in their heterogeneous structure and texture. The following microstructural types are distinguished by the variety and intensity of their deformation: protogranular → mesogranular → porphyroclastic → porphyrolath → mosaic. The petrostructural patterns of olivines pertaining to the above types reflect conditions of ductile deformation. Protogranular dunite is formed as a product of pyroxene decomposition in mantle harzburgite accompanied by annealing recrystallization at a temperature above 1000°C. Mesogranular dunite is formed as a product of high-temperature plastic flow by means of translation sliding in olivine and diffuse creep at a temperature dropping from 1000 to 650°C and at a low rate (<10-6 s-1). Cr-spinel segregates into linear zones of disseminated chromite mineralization within zones of bedding-plane plastic flow. Porphyroclastic and mosaic dunites are formed under conditions of intense deformation at a temperature of 500-750°C and at a significant rate (>10-6 s-1). Dunite is deformed by means of syntectonic recrystallization and subordinate translation gliding. Linear zones of disseminated mineralization undergo destruction thereby, with the formation of lenticular chromitite bodies from which ductile olivine is squeezed out with the formation of densely impregnated and massive ores.

  12. Ore petrology of chromite-PGE mineralization in the Kempirsai ophiolite complex

    NASA Astrophysics Data System (ADS)

    Distler, V. V.; Kryachko, V. V.; Yudovskaya, M. A.

    2008-01-01

    The platinum group minerals (PGM) in chromite ores of the Kempirsai ophiolite massif, located south of the Ural Mountains, are extremely varied in composition and represented predominantly by alloys, sulfides, arsenides, and sulfosalts of the iridium-group PGE (IPGE). The earlier Ir-Os-Ru alloys prevail over the later Cu-Os-Ru, Cu-Ir, Ni-Ir, Ni-Os-Ir-Ru, and Ni-Ru-Os-Fe alloys rich in base metals (BM). The earlier Ru-Os disulfides crystallize coevally with Ir-Os-Ru alloys, whereas the later sulfides are represented by compounds with a variable stoichiometry and a wide miscibility of Ni, Cu, Ir, Rh, Os, and Fe. Phase relations of PGE alloys with PGE-BM alloys, sulfides and sulfoarsenides confirm that deposition of these minerals was defined by a general evolution of PGE fractionation in the mineral-forming system but not by a super-imposed process. The leading mechanism of PGM crystallization is thought to be their dendritic growth during gas-transport reactions from low-density gaseous fluid enriched in PGE. The representative technological sampling of 0.5 million tons of an ore showed that the average PGE content in chromite ore is 0.71 ppm which leads to an evaluation of the PGE resources to be no less than 250 tons. Hence, the Kempirsai deposit is not only a giant chromium deposit, but also a giant deposit of IPGE: Ir, Ru, and Os. The size parameters of PGM and their aggregates suggests that the PGE may be recoverable in separate concentrates.

  13. Evaluation of potential toxicity and bioavailability of chromium in sediments associated with chromite ore processing residue.

    PubMed

    Becker, D Scott; Long, Edward R; Proctor, Deborah M; Ginn, Thomas C

    2006-10-01

    Recent studies by researchers at the U.S. Environmental Protection Agency and U.S. Geological Survey have evaluated the toxicity of Cr in freshwater and marine sediments, primarily during laboratory studies in which clean sediments were spiked with Cr. Results of those studies showed that Cr is relatively insoluble and nontoxic when present in the trivalent form, Cr(III), rather than in the more soluble and more toxic hexavalent form, Cr(VI). The studies concluded that Cr toxicity should be low in sediments with measurable concentrations of acid-volatile sulfide (AVS), because AVS is formed only in anoxic sediments and Cr(VI) is thermodynamically unstable under such conditions. The present study evaluates the toxicity and bioavailability of Cr in sediments associated with chromite ore processing residue (COPR). Ten stations were sampled in the Hackensack River (NJ, USA) to represent a wide range of total Cr concentrations (199-3,970 mg/kg) with minimal interference from potentially toxic, co-occurring chemicals. Sediment toxicity was evaluated using two amphipod tests: The 10-d Ampelisca abdita test (survival as endpoint), and the 28-d Leptocheirus plumulosus test (survival and biomass as endpoints). Measurable concentrations of AVS were present at eight stations, and nearly all Cr was present as Cr(III). In addition, results of electron-microprobe analyses showed that most Cr was associated with phases in which Cr has limited bioavailability (i.e., chromite and iron oxide). Sediment toxicity showed no correlation with concentrations of total Cr, and the maximum no-effect concentration for total Cr was estimated as 1,310 mg/ kg. These results indicate that Cr can be present in sediments associated with COPR at highly elevated concentrations without causing sediment toxicity.

  14. Lanthanum Deposition in the Stomach: Usefulness of Scanning Electron Microscopy for Its Detection.

    PubMed

    Iwamuro, Masaya; Urata, Haruo; Tanaka, Takehiro; Ando, Akemi; Nada, Takahiro; Kimura, Kosuke; Yamauchi, Kenji; Kusumoto, Chiaki; Otsuka, Fumio; Okada, Hiroyuki

    2017-02-01

    After having been treated with lanthanum carbonate administration for 4 years for hyperphosphatemia, a 75-year-old Japanese woman undergoing hemodialysis was diagnosed with lanthanum phosphate deposition in the stomach. The deposition, seen as white microgranules, was observed using esophagogastroduodenoscopy with magnifying observation. To the best of our knowledge, these are the minutest endoscopy images of lanthanum phosphate deposition in the gastric mucosa. Scanning electron microscopy (SEM) observation enabled easier identification of the deposited material, which was visible as bright areas. The present case suggests the usefulness of SEM observation in the detection of lanthanum phosphate deposition in the gastrointestinal tract.

  15. Nanoscale assembly of lanthanum silica with dense and porous interfacial structures

    PubMed Central

    Ballinger, Benjamin; Motuzas, Julius; Miller, Christopher R.; Smart, Simon; Diniz da Costa, João C.

    2015-01-01

    This work reports on the nanoscale assembly of hybrid lanthanum oxide and silica structures, which form patterns of interfacial dense and porous networks. It was found that increasing the molar ratio of lanthanum nitrate to tetraethyl orthosilicate (TEOS) in an acid catalysed sol-gel process alters the expected microporous metal oxide silica structure to a predominantly mesoporous structure above a critical lanthanum concentration. This change manifests itself by the formation of a lanthanum silicate phase, which results from the reaction of lanthanum oxide nanoparticles with the silica matrix. This process converts the microporous silica into the denser silicate phase. Above a lanthanum to silica ratio of 0.15, the combination of growth and microporous silica consumption results in the formation of nanoscale hybrid lanthanum oxides, with the inter-nano-domain spacing forming mesoporous volume. As the size of these nano-domains increases with concentration, so does the mesoporous volume. The absence of lanthanum hydroxide (La(OH)3) suggests the formation of La2O3 surrounded by lanthanum silicate. PMID:25644988

  16. Photocatalytic activity of SrTiO3 codoped with nitrogen and lanthanum under visible light illumination.

    PubMed

    Miyauchi, Masahiro; Takashio, Minoru; Tobimatsu, Hiroki

    2004-01-06

    Yellow SrTiO3 powders codoped with nitrogen and lanthanum (STO:N,La) were studied as visible light photocatalysts. The crystal phase of STO:N,La exhibited a pure perovskite phase, and O and Sr sites atoms were substitutionally doped with N and La atoms, respectively. The first principle calculation of STO:N,La indicated that the edge of the N(2p) band is situated above the valence band, which consisted of O(2p) orbitals, and the La orbitals did not exist in the band gap of SrTiO3. STO:N,La exhibited a higher oxidation activity of gaseous 2-propanol under vis illumination than SrTiO3 doped only with nitrogen (STO:N). The high activity of STO:N,La was due to the decrease in the oxygen vacancies, which acted as electron-hole recombination centers, because codoping with La3+ and N3- ions maintained the charge balance. The optimum doping density of N and La for visible light activity was 0.5%, and STO:N,La(0.5%) had an activity under UV illumination similar to pure SrTiO3.

  17. Geology and economic potential for chromite in the Zhob Valley ultramafic rock complex, Hindubagh, Quetta division, West Pakistan

    USGS Publications Warehouse

    Rossman, D.L.; Ahmad, Zaki; Rahman, Hamidur

    1971-01-01

    The ultramafic rocks making up the Zhob Valley igneous complex have yielded small amounts of metallurgical-grade chromite since the early part of the century. From 1968-1970 a cooperative study undertaken by the Geological Survey of Pakistan and the U. S. Geological Survey, under the auspices of the Government of Pakistan and the Agency for International Development, evaluated the chromite potential of the Zhob Valley area and provided data for effective exploration. The Jung Tor Ghar ultramafic rock mass, covering an area of about 45 square miles, is a thrust-fault block completely surrounded and underlain (?) by sedimentary rocks as young as Late Cretaceous in age. The igneous rocks were thrust from the northwest along an east-trending, north-dipping fault in Late Cretaceous or Paleocene time and were peneplaned, dissected, and deeply laterized by mid-Eocene time. The ultramafic rocks consist of interlayered harzburgite and dunite and a cross-cutting dunite here called transgressive dunite. Layered structure passes without discernible deviation from the interlayered harzburgite-dunite through the transgressive dunite. The lowest rocks in the mass, composed mainly of transgressive dunite, grade upward into the interlayered rock about 3,000 feet above the fault block base. The upper transgressive dunites tend to form interconnecting linear networks and probably a few pipe-like structures. The transgressive dunite is thought to have formed by action of water derived from the underlying sedimentary rocks; the water heated by the hot ultramafic rock (at the time of emplacement) altered the pyroxene to olivine and talc, and, with lowering temperature, to serpentine. Other interpretations are possible. Virtually all the chromite in the Jung Tor Ghar lies in or immediately above the masses of transgressive dunite. This fact provides a key to chromite exploration: The most favorable zone for prospecting lies in the vicinity of the upper contacts of the transgressive

  18. Physicochemical parameters of the melts participating in the formation of chromite ore hosted in the Klyuchevsky ultramafic massif, the Central Urals, Russia

    NASA Astrophysics Data System (ADS)

    Simonov, V. A.; Ivanov, K. S.; Smirnov, V. N.; Kovyazin, S. V.

    2009-04-01

    The results of melt inclusion study are reported for chromites of the Klyuchevsky ultramafic massif, which is the most representative of all Ural ultramafic massifs localized beyond the Main Ural Fault Zone. The massif is composed of a dunite-harzburgite complex (tectonized mantle peridotite) and a dunite-wehrlite-clinopyroxenite-gabbro complex (layered portion of the ophiolitic section). The studied Kozlovsky chromite deposit is located in the southeastern part of the Klyuchevsky massif and hosted in serpentinized dunite as a series of lenticular bodies and layers up to 7-8 m thick largely composed of disseminated and locally developed massive ore. Melt inclusions have been detected in chromites of both ore types. The heated and then quenched into glass melt inclusions and host minerals were analyzed on a Camebax-Micro microprobe. The glasses of melt inclusions contain up to 1.06 wt % Na2O + K2O and correspond to melts of normal alkalinity. In SiO2 content (49-56 wt %), they fit basalt and basaltic andesite. The melt inclusions are compared with those from chromites of the Nurali massif in the southern Urals and the Karashat massif in southern Tuva. The physicochemical parameters of magmatic systems related to the formation of disseminated and massive chromite ores of the Klyuchevsky massif are different. The former are characterized by a wider temperature interval (1185-1120°C) in comparison with massive chromite ore (1160-1140°C).

  19. Lanthanum(III) catalysts for highly efficient and chemoselective transesterification.

    PubMed

    Hatano, Manabu; Ishihara, Kazuaki

    2013-03-11

    A facile, atom-economical, and chemoselective esterification is crucial in modern organic synthesis, particularly in the areas of pharmaceutical, polymer, and material science. However, a truly practical catalytic transesterification of carboxylic esters with various alcohols has not yet been well established, since, with many conventional catalysts, the substrates are limited to 1°- and cyclic 2°-alcohols. In sharp contrast, if we take advantage of the high catalytic activities of La(Oi-Pr)(3), La(OTf)(3), and La(NO(3))(3) as ligand-free catalysts, ligand-assisted or additive-enhanced lanthanum(III) catalysts can be highly effective acid-base combined catalysts in transesterification. A highly active dinuclear La(III) catalyst, which is prepared in situ from lanthanum(III) isopropoxide and 2-(2-methoxyethoxy)ethanol, is effective for the practical transesterification of methyl carboxylates, ethyl acetate, weakly reactive dimethyl carbonate, and much less-reactive methyl carbamates with 1°-, 2°-, and 3°-alcohols. As the second generation, nearly neutral "lanthanum(III) nitrate alkoxide", namely La(OR)(m)(NO(3))(3-m), has been developed. This catalyst is prepared in situ from inexpensive, stable, low-toxic lanthanum(III) nitrate hydrate and methyltrioctylphosphonium methyl carbonate, and is highly useful in the non-epimerized transesterification of α-substituted chiral carboxylic esters, even under azeotropic reflux conditions. In these practical La(III)-catalyzed transesterifications, colorless esters can be obtained in small- to large-scale synthesis without the need for inconvenient work-up or careful purification procedures.

  20. Effect of heterovalent substitutions in yttrium chromite on the hyperfine interactions of {sup 119}Sn{sup 4+} studied by Mössbauer spectroscopy

    SciTech Connect

    Fabritchnyi, Pavel B.; Afanasov, Mikhail I.; Mezhuev, Evgeny M.; Wattiaux, Alain; Duttine, Mathieu; Labrugère, Christine

    2016-03-15

    In order to develop the {sup 119}Sn Mössbauer spectroscopic probe technique to study magnetically ordered materials, three Ca-substituted yttrium chromites, i.e. Y{sub 0.9}Ca{sub 0.1}CrO{sub 3}, Y{sub 0.9}Ca{sub 0.1}Cr{sub 0.9}Ti{sub 0.1}O{sub 3} and Y{sub 0.8}Ca{sub 0.2}Cr{sub 0.8}Ti{sub 0.2}O{sub 3}, doped with 0.3 atom-% Sn{sup 4+}, were for the first time investigated. {sup 119}Sn Mössbauer spectra, recorded at 4.2 K, have allowed, through analysis of the magnetic hyperfine field values, probed by {sup 119}Sn nuclei, to gain insight into the local magnetically active surrounding of different Sn{sup 4+} ions. In all of these compounds, partial segregation of Sn{sup 4+} ions is revealed. In the case of Y{sub 0.9}Ca{sub 0.1}CrO{sub 3}, neither highly oxidized Cr{sup 4+} nor Cr{sup 6+} species, expected to compensate for the Ca{sup 2+} positive charge deficit, is found in the vicinity of the {sup 119}Sn{sup 4+} probe. In the case of both studied Ti-containing chromites, {sup 119}Sn Mössbauer spectra have provided the original indirect evidence for the statistical distribution of Cr{sup 3+} and Ti{sup 4+} ions over the octahedral sites and permitted characterization of the occurring associates of Sn{sup 4+}. - Graphical abstract: Two kinds of Sn{sup 4+} associates allowing {sup 119}Sn Mössbauer spectra of tin-doped Y{sub 0.9}Ca{sub 0.1}Cr{sub 0.9}Ti{sub 0.1}O{sub 3} and Y{sub 0.8}Ca{sub 0.2}Cr{sub 0.8}Ti{sub 0.2}O{sub 3} to be accounted for. - Highlights: • {sup 119}Sn probe is tested as a source of information on the B-sublattice of AF perovskites. • Neither Cr{sup 3+} nor Cr{sup 6+} is detected nearby {sup 119}Sn{sup 4+} ions in Y{sub 0.9}Ca{sub 0.1}CrO{sub 3}. • Cr{sup 3+} and Ti{sup 4+} are found to be randomly distributed in Y{sub 1−x}Ca{sub x}Cr{sub 1−x}Ti{sub x}O{sub 3} (x=0.1 or 0.2). • Sn{sup 4+} dopant segregations are revealed in all of the studied materials.

  1. Infrared luminescence of Tm{sup 3+}/Yb{sup 3+} codoped lanthanum aluminum germanate glasses

    SciTech Connect

    Zhang Qiang; Zhang Guang; Chen Guorong; Qiu Jianrong; Chen Danping

    2010-01-15

    Tm{sup 3+} doped and Tm{sup 3+}/Yb{sup 3+} codoped lanthanum aluminum germanate (LAG) glasses are prepared by melt-quenching method and characterized optically. Based on the measurement of absorption spectrum, Judd-Ofelt intensity parameters ({Omega}{sub 2},{Omega}{sub 4},{Omega}{sub 6}) are calculated. The radiation emission rates, branching ratios, and lifetimes of Tm{sup 3+} are calculated to evaluate the spectroscopic properties of Tm{sup 3+} in LAG glass. The infrared emission properties of the samples are investigated and the results show that the 1.8 {mu}m emission can be greatly enhanced by adding proper amount of Yb{sup 3+} under the excitation of 980 nm. The energy transfer processes of Yb{sup 3+}-Yb{sup 3+} and Yb{sup 3+}-Tm{sup 3+} are analyzed, and the results show that Yb{sup 3+} ions can transfer their energy to Tm{sup 3+} ions with high efficiency and large energy transfer coefficient.

  2. Comparative Planetary Mineralogy: V/(Cr+Al) Systematics in Chromites as an Indicator of Relative Oxygen Fugacity

    NASA Technical Reports Server (NTRS)

    Papike, J. J.; Kamer, J. M.; Shearer, C. K.

    2004-01-01

    As our contribution to the new "Oxygen in the Solar System" initiative of the Lunar and Planetary Institute and the NASA Cosmochemistry Program, we have been developing oxygen barometers based largely on behavior of V which can occur in four valence states V2+, V3+, V4+, and V5+, and record at least 8 orders of magnitude of fO2. Our first efforts in measuring these valence proportions were by XANES techniques in basaltic glasses from Earth, Moon, and Mars. We now address the behavior of V valence states in chromite in basalts from Earth, Moon, and Mars. We have been looking for a "V in chromite oxybarometer" that works with data collected by the electron microprobe and thus is readily accessible to a large segment of the planetary materials community. This paper describes very early results that will be refined over the next two years.

  3. Distribution of platinum-group elements in the Bati Kef chromite deposit, Guleman-Elazig area, eastern Turkey.

    USGS Publications Warehouse

    Page, N.J.; Engin, T.; Singer, D.A.; Haffty, J.

    1984-01-01

    The distribution of platinum-group elements (PGE) within chromite deposits from an ophiolite is determined and their geochemistry compared with chromitites from ophiolites and from stratiform layered complexes elsewhere in the world. The Guleman area chromitites are lenses of layered massive to disseminated chromite in dunite or sheared harzburgite along and near the dunite-harzburgite contact. PGE were analysed by a fire assay/spectrographic method. The analyses, in ppb, varied narrowly near the detection limits; only Ir was mostly detected (24-27 ppb) . The data plot as independent, slight variations of individual PGE with crude and irregular spatial distributions, oriented with respect to the land surface. Based on studies elsewhere, the PGE reside mostly in laurite, erlichmanite and Os/Ir alloys included within or interstitial to chromite. Average values for each PGE were normalized with respect to average chondrite concentrations for these elements. All patterns for ophiolite-chromitites (5) show depletion of these elements relative to chondrite average concentrations, with greater depletion in Pt and Pd than in Ir and Ru, to produce patterns with negative slopes. Chromitites from differentiated stratiform complexes (2) yield patterns with positive slopes. -G.J.N.

  4. Ethanol Gas Sensor Based on Pure and La-Doped Bismuth Vanadate

    NASA Astrophysics Data System (ADS)

    Golmojdeh, Hosein; Zanjanchi, Mohamad Ali

    2014-02-01

    Bismuth vanadate (BiVO4) and lanthanum-doped bismuth vanadate (La-doped BiVO4) were prepared via the precipitation method. Their films were produced by simple drop-coating of the initial solutions over gold electrodes, which were coated over a glass substrate. The structural properties of BiVO4 and La-doped BiVO4 samples were studied using x-ray diffractometer, diffuse reflectance spectroscopy, scanning electron microscopy, atomic force microscopy, and compositional analysis. A chamber was designed to install the sensing device and also controllable tools for gas flow rate and temperature. Changes in the resistance of the prepared layers were recorded during exposure to various amounts of ethanol vapor at different temperatures. Both BiVO4 and La-doped BiVO4 layers showed measurable responses in the form of resistance drop (increased conductivity). The higher temperatures up to 450 °C led to stronger signals. The layer containing lanthanum showed signals with shorter recovery times. Introduction of lanthanum caused smaller crystallite sizes in addition to the formation of tetragonal phase of BiVO4. Presence of lanthanum increased the amounts of grain boundaries, magnitude of the response, and sensitivity. Sensitivity of La-doped BiVO4 was almost twice that of the BiVO4 at concentrations of 150-500 ppm of ethanol. Also, the correlation of the response as a function of concentration of ethanol in gas phase was exploited, and two different linear ranges were observed for the lower and higher concentrations.

  5. Effect of anode firing on the performance of lanthanum and nickel co-doped SrTiO3 (La0.2Sr0.8Ti0.9Ni0.1O3-δ) anode of solid oxide fuel cell

    NASA Astrophysics Data System (ADS)

    Park, Byung Hyun; Choi, Gyeong Man

    2015-10-01

    Perovskite oxides have potential for use as alternative anode materials in solid oxide fuel cells (SOFCs) due to stability in anode atmosphere; donor-doped SrTiO3 (e.g., La0.2Sr0.8TiO3-δ) is a good candidate for this purpose. Electro-catalytic nanoparticles can be produced in oxide anodes by the ex-solution method, e.g., by incorporating Ni into a perovskite oxide in air, then reducing the oxide in H2 atmosphere. In this study, we varied the temperature (1100, 1250 °C) and atmosphere (air, H2) of La0.2Sr0.8Ti0.9Ni0.1O3-δ (LSTN) anode firing to control the degree of Ni ex-solution and microstructure. LSTN fired at 1250 °C in H2 showed the best anodic performance for scandia-stabilized zirconia (ScSZ) electrolyte-supported cells in H2 and CH4 fuels due to the favorable microstructure and Ni ex-solution.

  6. Excess Nd and Eu Concentrations Discovered in Chromite Deposits from the Beyagaç District, Denizli region, SW Turkey

    NASA Astrophysics Data System (ADS)

    Kumral, M.; Karadaǧ, A.; Soyal, M.; Caran, Ş.; Akay, A. K.; Karabel, S. B.; Elmas, N.; Karaman, M.; Budakoglu, M.

    2012-04-01

    Chromite ore and associated ultramafic rocks from the Beyağaç district (Denizli, SW Turkey), have been analysed for major and trace element concentrations. The study area covers around 30 km2 in Aşağı Günlüce village, which is located three and a half kilometers west of the Beyağaç town of Denizli region. Lithological units in research area comprise, from oldest to youngest, Crateseous aged ophiolites, intrusive gabbros in ophiolites, mostly Mesozoic aged limestone units and Quaternary aged alluvials. Chromite mineralization in research site occurs mainly as massive, nodular and disseminated type ores. Chromite mineralizations present as bedded podiform types, and compositionally Cr2O3 values range between 18 and 50 wt.%. The obtained compositions of the ore chromite include Cr2O3 23.74-50.8 wt.%, MgO 0.15-1.1 wt.%, SiO2 11.39 wt.%,Fe2O3 12.50 - 36.61 wt.%, TiO2 0.16-0.77 wt.%, Al2O3 6.74-16.00 wt.%, CaO 9,69 wt.%, P2O5 0.01 wt.%, MnO 0,10-0,57 wt.% , LOI 10 wt.% as major oxides, and Ag 37-76 ppm, Cl 121-386 ppm, S 36-118 ppm, Ni 1271-2279 ppm, Cu 21-32 ppm, W 6-68 ppm, Sr 14-195 ppm, V 44-794 ppm, Zn 86-316 ppm, Sm 236 ppm, Ga 32 ppm as trace elements. High rates of Al2O3 (9,58 wt.%) , Fe2O3 (10,50 wt.%), K2O (0,19 wt.%), TiO2 (0,77 wt.%), P2O5 (0,10 wt.%), Ag (46 ppm), Cl (227 ppm), V (269 ppm), Zr (46 ppm) and Sr (173 ppm) are observed in ultramafic rock samples. The rate of Cr2O3 in a mixtured sample of both chromite vein and dunite, range between 0,16 and 0,69 wt.%. The most striking results are obtained from one sample, in which the Nd and Eu element values range between 236-1235 ppm for Nd and between 2100-2800 ppm for Eu.

  7. A search for H-chondritic chromite grains in sediments that formed immediately after the breakup of the L-chondrite parent body 470 Ma ago

    NASA Astrophysics Data System (ADS)

    Heck, Philipp R.; Schmitz, Birger; Rout, Surya S.; Tenner, Travis; Villalon, Krysten; Cronholm, Anders; Terfelt, Fredrik; Kita, Noriko T.

    2016-03-01

    A large abundance of L-chondritic material, mainly in the form of fossil meteorites and chromite grains from micrometeorites, has been found in mid-Ordovician 470 Ma old sediments globally. The material has been determined to be ejecta from the L chondrite parent body breakup event, a major collision in the asteroid belt 470 Ma ago. In this study we search the same sediments for H-chondritic chromite grains in order to improve our understanding of the extraterrestrial flux to Earth after the asteroid breakup event. We have used SIMS in conjunction with quantitative SEM/EDS to determine the three oxygen isotopic and elemental compositions, respectively, of a total of 120 randomly selected, sediment-dispersed extraterrestrial chromite grains mainly representing micrometeorites from 470 Ma old post-breakup limestone from the Thorsberg quarry in Sweden and the Lynna River site in Russia. We show that 99% or more of the grains are L-chondritic, whereas the H-chondritic fraction is 1% or less. The L-/H-chondrite ratio after the breakup thus was >99 compared to 1.1 in today's meteoritic flux. This represents independent evidence, in agreement with previous estimates based on sediment-dispersed extraterrestrial chromite grain abundances and sedimentation rates, of a two orders of magnitude higher post-breakup flux of L-chondritic material in the micrometeorite fraction. Finally, we confirm the usefulness of three oxygen isotopic SIMS analyses of individual extraterrestrial chromite grains for classification of equilibrated ordinary chondrites. The H- and L-chondritic chromites differ both in their three oxygen isotopic and elemental compositions, but there is some overlap between the groups. In chromite, TiO2 is the oxide most resistant to diagenesis, and the combined application of TiO2 and oxygen three-isotope analysis can resolve uncertainties arising from the compositional overlaps.

  8. Behavior of iron-group elements, oxybarometry, and genesis of unique chromite deposits in the Kempirsai massif

    NASA Astrophysics Data System (ADS)

    Chashchukhin, I. S.; Votyakov, S. L.

    2009-04-01

    Ultramafic rocks and high-Cr chromite ore from the Almaz-Zhemchuzhina deposit, the largest in the Main ore field of the Kempirsai massif, have been studied. The detailed mineralogical and geochemical examination of deep structure test and exploratory boreholes allowed us to establish the rough stratification of ultramafic rocks and to demonstrate the position of unique chromite deposits in the generalized vertical section of the southeastern Kempirsai massif. From top to bottom, a barren harzburgite-lherzolite series gives way to an ore-bearing dunite-harzburgite complex with the largest chromite deposits, including the unique Almaz-Zhemchuzhina deposit, in its upper portion and then to pyroxene-free dunite densely impregnated with chromite in the upper part and containing sparsely disseminated chromite at its base. The lower unit is composed of a barren lherzolite-harzburgite series transformed into blastomylonites near the contact with dunite, suggesting a tectonically doubled section in the southeastern part of the massif. The synore asymmetric geochemical zoning developed in the course of formation of chromite deposits as a result of removal of oreforming iron-group elements from the underlying and wall ultramafic rocks into the overlying rocks. Host rocks with disturbed initial proportions of Cr, Fe, Ni, and Mn, together with orebodies, made up ore-bearing zones no less than 1 km in thickness and subdivided into supra-, inter-, and subore subzones. The subore and wall rocks are characterized by partial loss (wt %) of Cr2O3(0.1), NiO (0.04), FeOtot(0.5), and MnO (0.02) and their removal into the interore and supraore (0.03 NiO) subzones. Thus, the subore ultramafic rocks served as a source of ore-forming components, while the interore zone with orebodies occurring therein served as a zone of discharge of these components. Using Mössbauer spectroscopy, the crystal chemistry of iron ions was studied in a representative selection of Cr-spinel samples from rocks

  9. Evaluation of the treatment of chromite ore processing residue by ferrous sulfate and asphalt.

    PubMed

    Moon, Deok Hyun; Wazne, Mahmoud; Koutsospyros, Agamemnon; Christodoulatos, Christos; Gevgilili, Halil; Malik, Moinuddin; Kalyon, Dilhan M

    2009-07-15

    The effectiveness of the treatment of chromite ore processing residue (COPR) with ferrous sulfate and encapsulation into asphalt were explored separately and in combination. The asphalt treatment was conducted by mixing COPR or ferrous sulfate pretreated COPR with varying amounts of asphalt. To assess the efficacy of the treatment, the leachability of toxicity characteristic leaching procedure (TCLP) total chromium (Cr) from all treated samples was determined for curing periods up to 16 months. X-ray absorption near edge structure (XANES) analyses were also performed to evaluate the Cr(6+) concentration in the selected samples. The combination treatment of ferrous sulfate and the encapsulation of the treated COPR into asphalt reduced the TCLP total Cr concentration to lower than the regulatory limit of 5mg/L for Cr contaminated soils, after 16 months. However, the Cr concentrations were still higher than the universal treatment standards (UTS) of 0.6 mg/L for hazardous waste. On the other hand, treatment with ferrous sulfate alone or the encapsulation of the COPR in asphalt failed to meet the TCLP total Cr concentration of 5mg/L, after 16 months. XANES analyses results showed that more than 75% Cr(6+) reduction was achieved upon pretreatment with ferrous sulfate.

  10. Reduction and immobilization of chromate in chromite ore processing residue with nanoscale zero-valent iron.

    PubMed

    Du, Jingjing; Lu, Jinsuo; Wu, Qiong; Jing, Chuanyong

    2012-05-15

    Chromite ore processing residue (COPR) poses a great environmental and health risk with persistent Cr(VI) leaching. To reduce Cr(VI) and subsequently immobilize in the solid matrix, COPR was incubated with nanoscale zero-valent iron (nZVI) and the Cr(VI) speciation and leachability were studied. Multiple complementary analysis methods including leaching tests, X-ray powder diffraction, X-ray absorption near edge structure (XANES) spectroscopy, and X-ray photoelectron spectroscopy (XPS) were employed to investigate the immobilization mechanism. Geochemical PHREEQC model calculation agreed well with our acid neutralizing capacity experimental results and confirmed that when pH was lowered from 11.7 to 7.0, leachate Cr(VI) concentrations were in the range 358-445mgL(-1) which contributed over 90% of dissolved Cr from COPR. Results of alkaline digestion, XANES, and XPS demonstrated that incubation COPR with nZVI under water content higher than 27% could result in a nearly complete Cr(VI) reduction in solids and less than 0.1mgL(-1) Cr(VI) in the TCLP leachate. The results indicated that remediation approaches using nZVI to reduce Cr(VI) in COPR should be successful with sufficient water content to facilitate electron transfer from nZVI to COPR.

  11. Probing structural distortions in rare earth chromites using Indian synchrotron radiation source

    NASA Astrophysics Data System (ADS)

    Late, R.; Rai, H. M.; Saxena, S. K.; Kumar, R.; Sagdeo, A.; Sagdeo, P. R.

    2016-12-01

    Effect of R site ionic radius on the structural distortions in RCrO3 (R: La, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Yb and Y) rare earth perovskite chromites is investigated through synchrotron based X-ray diffraction technique. The said structural distortions are measured in the terms of CrO bond lengths, CrO6 octahedral tilt, tolerance factor ( t) and RO12 polyhedral distortion. It is observed that the lattice parameters (b and c), RO bond length, tolerance factor and Cr-O-Cr bond angle increases with increase in the radius of R site ion; whereas octahedral tilts (along [010] and [101]) and RO12 polyhedral distortion decreases with increase in the radius of R site ion. Further it is observed that the radius of R site cation does not have significant effect on lattice parameter `a' and CrO bond length (hence on the distortion of CrO6 octahedra). A comparison of the crystal structure parameters obtained using refinement of synchrotron powder X-ray data and that estimated theoretically using modern bond valence parameters (SPuDS) has been carried out. A one to one correlation between the experimental and theoretical results has been observed.

  12. Microstructural analyses of Cr(VI) speciation in chromite ore processing Residue (COPR)

    SciTech Connect

    CHRYSOCHOOU, MARIA; FAKRA, SIRINE C .; Marcus, Matthew A.; Moon, Deok Hyun; Dermatas, Dimitris

    2010-03-01

    The speciation and distribution of Cr(VI) in the solid phase was investigated for two types of chromite ore processing residue (COPR) found at two deposition sites in the United States: gray-black (GB) granular and hard brown (HB) cemented COPR. COPR chemistry and mineralogy were investigated using micro-X-ray absorption spectroscopy and micro-X-ray diffraction, complemented by laboratory analyses. GB COPR contained 30percent of its total Cr(VI) (6000 mg/kg) as large crystals(>20 ?m diameter) of a previously unreported Na-rich analog of calcium aluminum chromate hydrates. These Cr(VI)-rich phases are thought to be vulnerable to reductive and pH treatments. More than 50percent of the Cr(VI) was located within nodules, not easily accessible to dissolved reductants, and bound to Fe-rich hydrogarnet, hydrotalcite, and possibly brucite. These phases are stable over a large pH range, thus harder to dissolve. Brownmilleritewasalso likely associated with physical entrapment of Cr(VI) in the interior of nodules. HB COPR contained no Cr(VI)-rich phases; all Cr(VI) was diffuse within the nodules and absent from the cementing matrix, with hydrogarnet and hydrotalcite being the main Cr(VI) binding phases. Treatment ofHBCOPRis challenging in terms of dissolving the acidity-resistant, inaccessible Cr(VI) compounds; the same applies to ~;;50percent of Cr(VI) in GB COPR.

  13. Assessment of calcium polysulfide for the remediation of hexavalent chromium in chromite ore processing residue (COPR).

    PubMed

    Wazne, Mahmoud; Jagupilla, Santhi Chandra; Moon, Deok Hyun; Jagupilla, Sarath Chandra; Christodoulatos, Christos; Kim, Min Gyu

    2007-05-17

    Bench scale and pilot scale treatability studies were conducted to evaluate the remediation of hexavalent chromium [Cr(VI)] in chromite ore processing residue (COPR) using calcium polysulfide. The results from the bench scale study indicated that a calcium polysulfide dosage twice the molar stoichiometric requirement (2x) proved effective in meeting the New Jersey Department of Environmental Protection (NJDEP) total Cr(VI) and the Environmental Protection Agency (EPA) Toxicity Characteristic Leaching Procedure (TCLP) regulatory standards. The treatment results were more effective at pH 12 than at pH 9.5. X-ray powder diffraction (XRPD) and X-ray absorption near edge structure (XANES) spectroscopy were also used to assess the treatment performance. Based on the bench scale results, an ex-situ pugmill pilot program was implemented to evaluate the applicability of the calcium polysulfide treatment on a larger scale (1000-lb batch test). The pugmill treatment results met Cr(VI) and TCLP regulatory standards over a period of 15 months. XANES analysis indicated that approximately 62% of Cr(VI) was reduced by calcium polysulfide at stoichiometric ratio of 2x after a curing period of 10 months.

  14. Calcium polysulfide remediation of hexavalent chromium contamination from chromite ore processing residue.

    PubMed

    Graham, Margaret C; Farmer, John G; Anderson, Peter; Paterson, Edward; Hillier, Stephen; Lumsdon, David G; Bewley, Richard J F

    2006-07-01

    Past disposal of high-lime chromite ore processing residue (COPR) from a chemical works in S.E. Glasgow, UK, has led to continuing release of toxic and carcinogenic hexavalent chromium (Cr(VI)) to groundwaters which are highly contaminated with Cr(VI)O4(2-). Traditional methods of remediating Cr(VI)-contaminated land, e.g. using ferrous sulfate and organic matter, have had limited success in converting Cr(VI) to less harmful and insoluble Cr(III). This paper describes the first application of calcium polysulfide (CaS(x)) to the remediation of contaminated groundwater and high-lime COPR in a series of laboratory experiments, which have demonstrated the effectiveness of the treatment in quantitatively and rapidly reducing Cr(VI) to Cr(III) over the pH range (8-12.5) typically found at the sites. Cr(III)-organic complexes, present in groundwater at one location, were also effectively precipitated upon treatment with CaS(x). The potential for large-scale use of CaS(x) in the remediation of Cr(VI) from COPR is also discussed.

  15. Evaluation of ettringite-related swelling mechanisms for treated chromite ore processing residue.

    PubMed

    Moon, Deok Hyun; Wazne, Mahmoud; Dermatas, Dimitris; Sanchez, Adriana M; Cheong, Kyung Hoon; Park, Jeong-Hun

    2015-01-01

    Accelerated one-dimensional unconfined swell tests were conducted for ferrous sulfate chromite ore processing residue (COPR) field-treated samples. The field-treated samples were subjected to wet and dry cycles over 100 days to accelerate the lithification of the samples. Parallel laboratory experiments were performed to investigate the effects of mineralogy on COPR swell under controlled conditions. The field and laboratory samples were treated with ferrous sulfate at a ferrous-to-Cr(6+) molar stoichiometric ratios of eight (8×) and five (5×). X-ray powder diffraction (XRPD) and scanning electron microscopy (SEM)-energy dispersive X-ray spectroscopy (EDX) analyses were used to investigate the mineralogical changes upon treatment. The swell results indicated that significant COPR swelling was observed in all of the tested samples. The swelling was more pronounced in the 5× treated COPR sample than in the 8× treated COPR sample. Moreover, the laboratory-treated samples showed greater swelling behavior as compared with the field-treated samples, which was most probably due to the high dry density of the COPR, indicating that dry density was a more dominant factor than lithification. XRPD and SEM-EDX results confirmed that significant ettringite formation occurred in all treated samples.

  16. Microstructural analyses of Cr(VI) speciation in chromite ore processing residue (COPR).

    PubMed

    Chrysochoou, Maria; Fakra, Sirine C; Marcus, Matthew A; Moon, Deok Hyun; Dermatas, Dimitris

    2009-07-15

    The speciation and distribution of Cr(VI) in the solid phase was investigated for two types of chromite ore processing residue (COPR) found at two deposition sites in the United States: gray-black (GB) granular and hard brown (HB) cemented COPR. COPR chemistry and mineralogy were investigated using micro-X-ray absorption spectroscopy and micro-X-ray diffraction, complemented by laboratory analyses. GB COPR contained 30% of its total Cr(VI) (6000 mg/kg) as large crystals (>20 microm diameter) of a previously unreported Na-rich analog of calcium aluminum chromate hydrates. These Cr(VI)-rich phases are thought to be vulnerable to reductive and pH treatments. More than 50% of the Cr(VI) was located within nodules, not easily accessible to dissolved reductants, and bound to Fe-rich hydrogarnet, hydrotalcite, and possibly brucite. These phases are stable over a large pH range, thus harder to dissolve. Brownmillerite was also likely associated with physical entrapment of Cr(VI) in the interior of nodules. HB COPR contained no Cr(VI)-rich phases; all Cr(VI) was diffuse within the nodules and absent from the cementing matrix, with hydrogarnet and hydrotalcite being the main Cr(VI) binding phases. Treatment of HB COPR is challenging in terms of dissolving the acidity-resistant, inaccessible Cr(VI) compounds; the same applies to approximately 50% of Cr(VI) in GB COPR.

  17. Bioleaching of nickel and cobalt from lateritic chromite overburden using the culture filtrate of Aspergillus niger.

    PubMed

    Biswas, Supratim; Dey, Rajib; Mukherjee, Siddhartha; Banerjee, Pataki C

    2013-08-01

    Extraction of metals (Ni, Co) from chromite overburden of Sukinda mines of Orissa, India, with the culture filtrate of Aspergillus niger was studied. Results showed that the amounts of metals leached varied directly with reaction temperature and period of fermentation. The culture filtrate was analyzed for citric and oxalic acids, and contained only oxalic acid-the concentration of which increased with time. Although this acid played the major role in leaching of metals, other unidentified metabolites present in the culture filtrate influenced the dissolution of the metals significantly. Maximum recovery of metals from raw and roasted ore samples was achieved at 80 °C with the 21-day culture filtrate containing the highest amount of oxalic acid. Under identical experimental conditions, much higher amounts of the metals were leached from roasted ore. Microstructures of the ore particles were studied by scanning electron microscopy and transmission electron microscopy; the bonding behaviors of metal compounds were identified by Fourier transform infrared spectroscopy which showed that the metals were leached after chelation with oxalic acid.

  18. Swelling related to ettringite crystal formation in chromite ore processing residue.

    PubMed

    Moon, Deok Hyun; Dermatas, Dimitris; Wazne, Mahmoud; Sanchez, Adriana M; Chrysochoou, Maria; Grubb, Dennis G

    2007-08-01

    Several million tons of Chromite Ore Processing Residue (COPR) were deposited at two sites in New Jersey and Maryland, USA, and over time they exhibited extensive heaving phenomena. Ettringite, a needle-shaped mineral and an expansive mineral commonly recognized in the literature concerning cement- and soil, has been identified extensively in numerous COPR samples collected from these sites. It was therefore believed that ettringite formation and its crystal growth are strongly associated with COPR heaving. We investigated the correlation between ettringite and the heaving phenomena in COPR materials that contained no initial ettringite. Two identical COPR samples were exposed to a 4% w/w sulfate solution (25 degrees C, 50 degrees C) in a confined swell test apparatus. Both swell test samples were analyzed by means of X-ray powder diffraction. The peak intensities of newly formed ettringite were more pronounced in the sample tested at 50 degrees C, and swell development was only observed in this sample. Scanning electron microscopy analyses revealed well-crystallized ettringite needles exceeding 40 microm in length for this sample, while ettringite crystals less than 15 microm in length formed in the sample tested at 25 degrees C. Therefore, the results suggest that the quantity of ettringite and the extent of crystallization play a key role in the heave of COPR.

  19. Application of the Rietveld method to assess chromium(VI) speciation in chromite ore processing residue.

    PubMed

    Chrysochoou, Maria; Dermatas, Dimitris

    2007-03-15

    The Rietveld method allows the quantification of crystalline phases and amorphous material identified by X-ray powder diffraction (XRPD) and other diffraction methods. The method assists in determining the speciation of contaminants in solid matrices both qualitatively and quantitatively in a statistically defensible approach, as it does not focus on a microscale. Rietveld was applied to chromite ore processing residue (COPR), a cementitious waste containing hexavalent chromium. Calcium aluminum chromium oxide hydrates (CACs) were the crystalline phases identified by XRPD that bind Cr(6+) in COPR according to their chemical formula. Rietveld quantification, combined with mass balances on Cr(6+), showed that CACs may bind Cr(6+) in variable percentages, ranging from 25% to 85%. Analysis of duplicate samples showed that material variability is the predominant factor of uncertainty in evaluating the role of CACs in Cr(6+) speciation, provided that a consistent quantification strategy is pursued. The choice of strategy was performed on the basis of the pertinent literature, preliminary analyses of the equipment and the software settings, and mass balances. The correlation between the average CAC-bound Cr(6+) concentration and the total Cr(6+) for five samples (R(2)=0.94), extracted from different zones and soil borings, suggests that CACs are a primary sink for Cr(6+) in COPR.

  20. Ettringite-induced heave in chromite ore processing residue (COPR) upon ferrous sulfate treatment.

    PubMed

    Dermatas, Dimitris; Chrysochoou, Maria; Moon, Deok Hyun; Grubb, Dennis G; Wazne, Mahmoud; Christodoulatos, Christos

    2006-09-15

    A pilot-scale treatment study was implemented at a deposition site of chromite ore processing residue (COPR) in New Jersey. Ferrous sulfate heptahydrate (FeSO4 x 7H2O) was employed to reduce hexavalent chromium in two dosages with three types of soil mixing equipment. XANES analyses of treated samples cured for 240 days indicated that all treatment combinations failed to meet the Cr(VI) regulatory limit of 240 mg/kg. More importantly, the discrepancy between XANES and alkaline digestion results renders the latter unreliable for regulatory purposes when applied to ferrous-treated COPR. Regardless of Cr-(VI), the introduction of reductant containing sulfate, mechanical mixing, water, acidity, and the resulting temperature increase in treated COPR promoted dissolution of brownmillerite (Ca2FeAlO5), releasing alumina and alkalinity. The pH increase caused initially precipitated gypsum (CaSO4 x 2H2O) to progressively convert to ettringite (Ca6Al2(SO4)3 x 32H2O) and its associated volume expansion under both in situ and ex situ conditions, with a maximum of 0.8 m vertical swell within 40 days of curing. While Cr-(VI) treatment remains a challenge, the intentional exhaustion of the heave potential of COPR by transforming all Al sources to ettringite emerges as a possible solution to delayed ettringite formation, which would hamper site redevelopment.

  1. Evaluation of chromium bioaccessibility in chromite ore processing residue using in vitro gastrointestinal method.

    PubMed

    Yu, Siwu; Du, Jingjing; Luo, Ting; Huang, Yuying; Jing, Chuanyong

    2012-03-30

    Incidental ingestion of Chromite ore processing residue (COPR) particles poses a potential health risk. The purpose of this study was to determine the Cr bioaccessibility from COPR using the in vitro gastrointestinal (IVG) procedure. The bioaccessible Cr(VI) was 53.8% and 42.9%, respectively, in the gastric and intestinal phases from a total of 19490 mg kg(-1) Cr(VI) in COPR. Food intake including milk, dough, and ascorbic acid resulted in a significant decrease in Cr(VI) bioaccessibility. Some organic acids such as lactic, malic, and citric acid moderately reduced Cr(VI), while acetic acid exhibited no capacity for Cr(VI) reduction. The integrated area under the concentration-time curve (AUC) of the IVG extraction was used to calculate bioaccessibility. Compared with the bioaccessibility conventionally estimated using concentrations at the end of the extraction (CEP), the AUC technique should be implemented to confirm the accuracy of the IVG method when reduction of Cr(VI) occurs during the extraction. The absence of Cr(VI) phases in extracted residues as evidenced by XANES and XRPD analysis confirmed the Cr(VI) release and Cr(VI) reduction by food and ascorbic acid. With readily bioaccessible Cr(VI) and rapid human uptake, reduction of Cr(VI) might not be as effective a detoxification pathway as initially thought.

  2. Hexavalent chromium reduction by aerobic heterotrophic bacteria indigenous to chromite mine overburden

    PubMed Central

    Dey, Satarupa; Paul, A.K.

    2013-01-01

    Microbiological analysis of overburden samples collected from chromite mining areas of Orissa, India revealed that they are rich in microbial density as well as diversity and dominated by Gram-negative (58%) bacteria. The phenotypically distinguishable bacterial isolates (130) showed wide degree of tolerance to chromium (2–8 mM) when tested in peptone yeast extract glucose agar medium. Isolates (92) tolerating 2 mM chromium exhibited different degrees of Cr+6 reducing activity in chemically defined Vogel Bonner (VB) broth and complex KSC medium. Three potent isolates, two belonging to Arthrobacter spp. and one to Pseudomonas sp. were able to reduce more than 50 and 80% of 2 mM chromium in defined and complex media respectively. Along with Cr+6 (MIC 8.6–17.8 mM), the isolates showed tolerance to Ni+2, Fe+3, Cu+2 and Co+2 but were extremely sensitive to Hg+2 followed by Cd+2, Mn+2 and Zn+2. In addition, they were resistant to antibiotics like penicillin, methicillin, ampicillin, neomycin and polymyxin B. During growth under shake-flask conditions, Arthrobacter SUK 1201 and SUK 1205 showed 100% reduction of 2 mM Cr+6 in KSC medium with simultaneous formation of insoluble precipitates of chromium salts. Both the isolates were also equally capable of completely reducing the Cr+6 present in mine seepage when grown in mine seepage supplemented with VB concentrate. PMID:24159321

  3. Solidification/stabilization of chromite ore processing residue using alkali-activated composite cementitious materials.

    PubMed

    Huang, Xiao; Zhuang, RanLiang; Muhammad, Faheem; Yu, Lin; Shiau, YanChyuan; Li, Dongwei

    2017-02-01

    Chromite Ore Processing Residue (COPR) produced in chromium salt production process causes a great health and environmental risk with Cr(VI) leaching. The solidification/stabilization (S/S) of COPR using alkali-activated blast furnace slag (BFS) and fly ash (FA) based cementitious material was investigated in this study. The optimum percentage of BFS and FA for preparing the alkali-activated BFS-FA binder had been studied. COPR was used to replace the amount of BFS-FA or ordinary Portland cement (OPC) for the preparation of the cementitious materials, respectively. The immobilization effect of the alkali-activated BFS-FA binder on COPR was much better than that of OPC based cementitious material. The potential for reusing the final treatment product as a readily available construction material was evaluated. X-ray diffraction (XRD), Fourier transform infrared spectrometry (FTIR) and scanning electron microscope with energy dispersive spectrometer (SEM-EDS) analysis indicated that COPR had been effectively immobilized. The solidification mechanism is the combined effect of reduction, ion exchange, precipitation, adsorption and physical fixation in the alkali-activated composite cementitious material.

  4. METHOD OF SEPARATING PLUTONIUM FROM LANTHANUM FLUORIDE CARRIER

    DOEpatents

    Watt, G.W.; Goeckermann, R.H.

    1958-06-10

    An improvement in oxidation-reduction type methods of separating plutoniunn from elements associated with it in a neutron-irradiated uranium solution is described. The method relates to the separating of plutonium from lanthanum ions in an aqueous 0.5 to 2.5 N nitric acid solution by 'treating the solution, at room temperature, with ammonium sulfite in an amount sufficient to reduce the hexavalent plutonium present to a lower valence state, and then treating the solution with H/sub 2/O/sub 2/ thereby forming a tetravalent plutonium peroxide precipitate.

  5. Phase I. Lanthanum-based Start Materials for Hydride Batteries

    SciTech Connect

    Gschneidner, K. A.; Schmidt, F. A.; Frerichs, A. E.; Ament, K. A.

    2013-08-20

    The purpose of Phase I of this work is to focus on developing a La-based start material for making nickel-metal (lanthanum)-hydride batteries based on our carbothermic-silicon process. The goal is to develop a protocol for the manufacture of (La1-xRx)(Ni1-yMy)(Siz), where R is a rare earth metal and M is a non-rare earth metal, to be utilized as the negative electrode in nickel-metal hydride (NiMH) rechargeable batteries.

  6. Comparison of the Oxidation Behaviors of High FeO Chromite and Magnetite Concentrates Relevant to the Induration of Ferrous Pellets

    NASA Astrophysics Data System (ADS)

    Zhu, Deqing; Yang, Congcong; Pan, Jian; Li, Xiaobo

    2016-10-01

    Oxidation process plays an important role in producing sufficiently strong ferrous pellets for blast furnace, and the oxidation behavior of pellet feed greatly affects the quality of pellets. As a supplementary research to earlier published work, the present study fixes its particular attention on the fundamental oxidation behavior of a high FeO South African chromite concentrate in comparison to that of typical magnetite concentrate using differential scanning calorimetry, X-ray diffraction analysis, and thermogravimetry at various temperatures ranging from 473 K to 1273 K (200 °C to 1000 °C). The reaction mechanism and phase transformation during the oxidation process of chromite spinel is further explained by thermodynamics calculation performed by FactSage software. Besides, routine laboratory preheating-roasting test of single ore pellets is also conducted to reveal the relevance of oxidizability to the consolidation of pellets. The results show that the chromite spinel possesses much poorer oxidizability than magnetite, usually accompanying complex phase transformations via a preferential nucleation of Fe-rich sesquioxide from the chromite spinel matrix at low temperatures and thereafter the formation of Cr-rich sesquioxide on the substrate of Fe-rich phase at high temperatures. The oxidation of chromite spinel is inferior to that of magnetite from the viewpoint of thermodynamics and dynamic kinetics. Good inherent oxidizability of raw materials is found to have a positive effect on the induration process of pellet.

  7. Analytical and mineralogical studies of ore and impurities from a chromite mineral using X-ray analysis, electrochemical and microscopy techniques.

    PubMed

    Sánchez-Ramos, S; Doménech-Carbó, A; Gimeno-Adelantado, J V; Peris-Vicente, J

    2008-02-15

    A wide analytical study of South African chromite ore, material with high interest in ceramic industry, has been carried out. With this purpose, an accurate chemical identification and mineralogical characterization of the mineral and the gangue have been performed using X-ray fluorescence (XRF), voltammetry, X-ray diffraction (XRD), light microscopy (LM), and scanning electron microscopy (SEM/EDX). The elemental composition of the sample (ore and gangue) has been obtained by XRF. The voltammetric analysis has allowed to demonstrate that iron in the sample was as Fe(II). The main compound of the chromite ore was a spinel (magnesiochromite ferroan), identified by XRD from the sample, which constitutes the chromite ore. This technique has also been useful to characterize some silicates as impurities in the chromite ore sample. Light microscopy has allowed the detection of the spinel and the identification of a silicate impurity (chrome chlorite), by means of their colouration. On the other hand, the other silicate impurity was identified as labradorite by means of X-ray microscopy by SEM/EDX. Finally, a strategy was developed to calculate the composition of each mineral in the unknown sample. The obtained results were: chromite spinel 82.89%, chlorite 12.79% and labradorite 4.32%.

  8. Novel borothermal route for the synthesis of lanthanum cerium hexaborides and their field emission properties

    SciTech Connect

    Menaka; Patra, Rajkumar; Ghosh, Santanu; Ganguli, Ashok K.

    2012-10-15

    The present study describes the development of a simple approach to stabilize polycrystalline lanthanum cerium hexaborides without using any flux and at ambient pressure. The nanostructured lanthanum-cerium borides were synthesized using hydroxide precursors. These precursors (La{sub 1-x}Ce{sub x}(OH){sub 3}, x=0.1, 0.2, 0.3 and 0.5) were synthesized via hydrothermal route in the presence of Tergitol (surfactant, nonylphenol ethoxylate) as a capping agent. The precursors on heating with boron at 1300 Degree-Sign C lead to the formation of nanostructures (cubes, rods and pyramids) of lanthanum cerium hexaboride. We have investigated the field emission behaviour of the hexaboride films fabricated by spin coating. It was observed that the pyramidal shaped nanostructures of La{sub 0.5}Ce{sub 0.5}B{sub 6} shows excellent field emission characteristics with high field enhancement factor of 4502. - Graphical abstract: Nanostructured lanthanum cerium hexaboride with efficient field emission have fabricated by low temperature hydroxide precursor mediated route. Highlights: Black-Right-Pointing-Pointer New methodology to prepare lanthanum cerium hexaboride at 1300 Degree-Sign C via borothermal route. Black-Right-Pointing-Pointer Nanostructured lanthanum cerium hexaboride film by spin coating process. Black-Right-Pointing-Pointer Nanopyramids based lanthanum cerium hexaboride shows excellent field emission.

  9. Stability of solid oxide fuel cell materials

    SciTech Connect

    Armstrong, T.R.; Pederson, L.R.; Stevenson, J.W.; Raney, P.E.

    1995-08-01

    The phase stability and sintering behavior of materials used in SOFCs has been evaluated. The sintering behavior of Ca and Sr doped lanthanum. manganite (the preferred SOFC cathode material) is highly dependent on the relative proportion of A and B site cations in the material. Ca and Sr doped lanthanum chromite (the preferred interconnect material) have been shown to rapidly expand in reducing atmospheres at temperatures as low as 700{degrees}C. This expansion is due to the reduction of Cr{sup 4+} to Cr{sup 3+} in reducing environments.

  10. Trace-element fingerprints of chromite, magnetite and sulfides from the 3.1 Ga ultramafic-mafic rocks of the Nuggihalli greenstone belt, Western Dharwar craton (India)

    NASA Astrophysics Data System (ADS)

    Mukherjee, Ria; Mondal, Sisir K.; González-Jiménez, José M.; Griffin, William L.; Pearson, Norman J.; O'Reilly, Suzanne Y.

    2015-06-01

    The 3.1 Ga Nuggihalli greenstone belt in the Western Dharwar craton is comprised of chromitite-bearing sill-like ultramafic-mafic rocks that are surrounded by metavolcanic schists (compositionally komatiitic to komatiitic basalts) and a suite of tonalite-trondhjemite-granodiorite gneissic rocks. The sill-like plutonic unit consists of a succession of serpentinite (after dunite)-peridotite-pyroxenite and gabbro with bands of titaniferous magnetite ore. The chromitite ore-bodies (length ≈30-500 m; width ≈2-15 m) are hosted by the serpentinite-peridotite unit. Unaltered chromites from massive chromitites (>80 % modal chromite) of the Byrapur and Bhaktarhalli chromite mines in the greenstone belt are characterized by high Cr# (100Cr/(Cr + Al)) of 78-86 and moderate Mg# (100 Mg/(Mg + Fe2+)) of 45-55. In situ trace-element analysis (LA-ICPMS) of unaltered chromites indicates that the parental magma of the chromitite ore-bodies was a komatiite lacking nickel-sulfide mineralization. In the Ga/Fe3+# versus Ti/Fe3+# diagram, the Byrapur chromites plot in the field of suprasubduction zone (SSZ) chromites while those from Bhaktarhalli lie in the MOR field. The above results corroborate our previous results based on major-element characteristics of the chromites, where the calculated parental melt of the Byrapur chromites was komatiitic to komatiitic basalt, and the Bhaktarhalli chromite was derived from Archean high-Mg basalt. The major-element chromite data hinted at the possibility of a SSZ environment existing in the Archean. Altered and compositionally zoned chromite grains in our study show a decrease in Ga, V, Co, Zn, Mn and enrichments of Ni and Ti in the ferritchromit rims. Trace-element heterogeneity in the altered chromites is attributed to serpentinization. The trace-element patterns of magnetite from the massive magnetite bands in the greenstone belt are similar to those from magmatic Fe-Ti-V-rich magnetite bands in layered intrusions, and magnetites from

  11. Radio-opaque fecal impaction and pseudo-occlusion in a dialyzed patient taking lanthanum carbonate.

    PubMed

    Muller, Clotilde; Muller, Sandrine; Sissoko, Aicha; Klein, Alexandre; Faller, Bernadette; Chantrel, Francois

    2012-10-01

    Lanthanum therapy is an efficient therapy of hyperphosphoremia by chelating phosphore in the digestive tract. Lanthanum is a silvery white metallic element that belongs to group 3 of the periodic table. This drug is lightly absorbed and has low water solubility. It should be borne in mind that abdominal X-rays of patients taking lanthanum carbonate may have a radio-opaque appearance typical of imaging agents. This characteristic is suggested to confirm adherence of the patient by doing an abdominal X-ray. We describe in our case a particular good compliant patient with slow digestive transit, which ends by pseudo-occlusion.

  12. Lanthanum-hexaboride carbon composition for use in corrosive hydrogen-fluorine environments

    DOEpatents

    Holcombe, Cressie E.; Kovach, Louis; Taylor, Albert J.

    1981-01-01

    The present invention relates to a structural composition useful in corrosive hydrogen-fluorine environments at temperatures in excess of 1400.degree. K. The composition is formed of a isostatically pressed and sintered or a hot-pressed mixture of lanthanum hexaboride particles and about 10-30 vol. % carbon. The lanthanum-hexaboride reacts with the high-temperature fluorine-containing bases to form an adherent layer of corrosion-inhibiting lanthanum trifluoride on exposed surfaces of the composition. The carbon in the composite significantly strengthens the composite, enhances thermal shock resistance, and significantly facilitates the machining of the composition.

  13. Lanthanum-hexaboride carbon composition for use in corrosive hydrogen-fluorine environments

    DOEpatents

    Holcombe, C.E. Jr.; Kovach, L.; Taylor, A.J.

    1980-01-22

    The present invention relates to a structural composition useful in corrosive hydrogen-fluorine environments at temperatures in excess of 1400/sup 0/K. The composition is formed of a isostatically pressed and sintered or a hot-pressed mixture of lanthanum hexaboride particles and about 10 to 30 vol% carbon. The lanthanum-hexaboride reacts with the high-temperature fluorine-containing gases to form an adherent layer of corrosion-inhibiting lanthanum trifluoride on exposed surfaces of the composition. The carbon in the composite significantly strengthens the composite, enhances thermal shock resistance, and significantly facilitates the machining of the composition.

  14. The soda-ash roasting of chromite ore processing residue for the reclamation of chromium

    NASA Astrophysics Data System (ADS)

    Antony, M. P.; Tathavadkar, V. D.; Calvert, C. C.; Jha, A.

    2001-12-01

    Sodium chromate is produced via the soda-ash roasting of chromite ore with sodium carbonate. After the reaction, nearly 15 pct of the chromium oxide remains unreacted and ends up in the waste stream, for landfills. In recent years, the concern over environmental pollution from hexavalent chromium (Cr6+) from the waste residue has become a major problem for the chromium chemical industry. The main purpose of this investigation is to recover chromium oxide present in the waste residue as sodium chromate. Cr2O3 in the residue is distributed between the two spinel solid solutions, Mg(Al,Cr)2O4 and γ-Fe2O3. The residue from the sodium chromate production process was analyzed both physically and chemically. The compositions of the mineral phases were determined by X-ray diffraction (XRD), scanning electron microscopy (SEM), and electron probe microanalysis (EPMA). The influence of alkali addition on the overall reaction rate is examined. The kinetics of the chromium extraction reaction resulting from the residue of the soda-ash roasting process under an oxidizing atmosphere is also investigated. It is shown that the experimental results for the roasting reaction can be best described by the Ginstling and Brounshtein (GB) equation for diffusion-controlled kinetics. The apparent activation energy for the roasting reaction was calculated to be between 85 and 90 kJ·mol-1 in the temperature range 1223 to 1473 K. The kinetics of leaching of Cr3+ ions using the aqueous phase from the process residue is also studied by treating the waste into acid solutions with different concentrations.

  15. Long-term treatment issues with chromite ore processing residue (COPR): Cr(6+) reduction and heave.

    PubMed

    Moon, Deok Hyun; Wazne, Mahmoud; Dermatas, Dimitris; Christodoulatos, Christos; Sanchez, Adriana M; Grubb, Dennis G; Chrysochoou, Maria; Kim, Min Gyu

    2007-05-17

    A pugmill treatability study was conducted to remediate chromite ore processing residue (COPR) using ferrous sulfate heptahydrate (FeSO(4) x 7H(2)O) as a reductant. Two different types of COPR, with respect to particle size and mineralogy, were tested in this study. Two different stoichiometric ratios of FeSO(4) x 7H(2)O to Cr(6+) (5x and 8x) were applied to reduce Cr(6+) to Cr(3+). The effectiveness of FeSO(4).7H(2)O treatment was assessed using the toxicity characteristic leaching procedure (TCLP) tests and X-ray absorption near edge structure (XANES) analyses. TCLP results obtained from the pugmill treatability study showed that TCLP Cr concentrations were less than the TCLP regulatory limit of 5mg/L upon 8x FeSO(4) x 7H(2)O treatment for up to 420 days but may fail to meet this regulatory limit in the long-term. XANES results obtained from samples cured for 300 days showed that all of the treated samples failed the New Jersey Department of Environmental Protection (NJDEP) clean up level for Cr(6+) of 240 mg/kg. However, the Cr(6+) concentration from the sample with the smaller particle size approached 240 mg/kg (338 mg/kg), suggesting that particle size reduction prior to the addition of reductant may improve the effectiveness of the treatment. COPR heaving was investigated with unconfined swell tests upon 5x and 8x FeSO(4) x 7H(2)O treatment. The formation of ettringite, an expansive material, was investigated following the swell tests using X-ray powder diffraction (XRPD). Significant heaving (>50 vol%) was observed at curing times of 138 days for the 5x treatment and the ettringite formation was identified by XRPD analyses.

  16. Leaching mechanisms of Cr(VI) from chromite ore processing residue.

    PubMed

    Wazne, Mahmoud; Jagupilla, Santhi Chandra; Moon, Deok Hyun; Christodoulatos, Christos; Koutsospyros, Agamemnon

    2008-01-01

    Batch leaching tests, qualitative and quantitative x-ray powder diffraction (XRPD) analyses, and geochemical modeling were used to investigate the leaching mechanisms of Cr(VI) from chromite ore processing residue (COPR) samples obtained from an urban area in Hudson County, New Jersey. The pH of the leaching solutions was adjusted to cover a wide range between 1 and 12.5. The concentration levels for total chromium (Cr) and Cr(VI) in the leaching solutions were virtually identical for pH values >5. For pH values <5, the concentration of total Cr exceeded that of Cr(VI) with the difference between the two attributed to Cr(III). Geochemical modeling results indicated that the solubility of Cr(VI) is controlled by Cr(VI)-hydrocalumite and Cr(VI)-ettringite at pH >10.5 and by adsorption at pH <8. However, experimental results suggested that Cr(VI) solubility is controlled partially by Cr(VI)-hydrocalumite at pH >10.5 and by hydrotalcites at pH >8 in addition to adsorption of anionic chromate species onto inherently present metal oxides and hydroxides at pH <8. As pH decreased to <10, most of the Cr(VI) bearing minerals become unstable and their dissolution contributes to the increase in Cr(VI) concentration in the leachate solution. At low pH ( <1.5), Cr(III) solid phases and the oxides responsible for Cr(VI) adsorption dissolve and release Cr(III) and Cr(VI) into solution.

  17. Mobilization of Cr(VI) from chromite ore processing residue through acid treatment.

    PubMed

    Tinjum, James M; Benson, Craig H; Edil, Tuncer B

    2008-02-25

    Batch leaching studies on chromite ore processing residue (COPR) were performed using acids to investigate leaching of hexavalent chromium, Cr(VI), with respect to particle size, reaction time, and type of acid (HNO(3) and H(2)SO(4)). Aqueous Cr(VI) is maximized at approximately 0.04 mol Cr(VI) per kg of dry COPR at pH 7.6-8.1. Cr(VI) mobilized more slowly for larger particles, and the pH increased with time and increased more rapidly for smaller particles, suggesting that rate limitations occur in the solid phase. With H(2)SO(4), the pH stabilized at a higher value (8.8 for H(2)SO(4) vs. 8.0 for HNO(3)) and more rapidly (16 h vs. 30 h), and the differences in pH for different particle sizes were smaller. The acid neutralization capacity (ANC) of COPR is very large (8 mol HNO(3) per kg of dry COPR for a stable eluate pH of 7.5). Changes to the elemental and mineralogical composition and distribution in COPR particles after mixing with acid indicate that Cr(VI)-bearing solids dissolved. However, concentrations of Cr(VI) >2800 mg kg(-1) (>50% of the pre-treatment concentration) were still found after mixing with acid, regardless of the particle size, reaction time, or type of acid used. The residual Cr(VI) appears to be partially associated with poorly-ordered Fe and Al oxyhydroxides that precipitated in the interstitial areas of COPR particles. Remediation strategies that use HNO(3) or H(2)SO(4) to neutralize COPR or to maximize Cr(VI) in solution are likely to require extensive amounts of acid, may not mobilize all of the Cr(VI), and may require extended contact time, even under well-mixed conditions.

  18. Detoxification and immobilization of chromite ore processing residue in spinel-based glass-ceramic.

    PubMed

    Liao, Chang-Zhong; Tang, Yuanyuan; Lee, Po-Heng; Liu, Chengshuai; Shih, Kaimin; Li, Fangbai

    2017-01-05

    A promising strategy for the detoxification and immobilization of chromite ore processing residue (COPR) in a spinel-based glass-ceramic matrix is reported in this study. In the search for a more chemically durable matrix for COPR, the most critical crystalline phase for Cr immobilization was found to be a spinel solid solution with a chemical composition of MgCr1.32Fe0.19Al0.49O4. Using Rietveld quantitative X-ray diffraction analysis, we identified this final product is with the phases of spinel (3.5wt.%), diopside (5.2wt.%), and some amorphous contents (91.2wt.%). The partitioning ratio of Cr reveals that about 77% of the Cr was incorporated into the more chemically durable spinel phase. The results of Cr K-edge X-ray absorption near-edge spectroscopy show that no Cr(VI) was observed after conversion of COPR into a glass-ceramic, which indicates successful detoxification of Cr(VI) into Cr(III) in the COPR-incorporated glass-ceramic. The leaching performances of Cr2O3 and COPR-incorporated glass-ceramic were compared with a prolonged acid-leaching test, and the results demonstrate the superiority of the COPR-incorporated glass-ceramic matrix in the immobilization of Cr. The overall results suggest that the use of affordable additives has potential in more reliably immobilizing COPR with a spinel-based glass-ceramic for safer disposal of this hazardous waste.

  19. Assessment of ferrous chloride and Portland cement for the remediation of chromite ore processing residue.

    PubMed

    Jagupilla, Santhi C; Wazne, Mahmoud; Moon, Deok Hyun

    2015-10-01

    Chromite Ore Processing Residue (COPR) is an industrial waste containing up to 7% chromium (Cr) including up to 5% hexavalent chromium [Cr(VI)]. The remediation of COPR has been challenging due to the slow release of Cr(VI) from a clinker like material and thereby the incomplete detoxification of Cr(VI) by chemical reagents. The use of sulfur based reagents such as ferrous sulfate and calcium polysulfide to detoxify Cr(VI) has exasperated the swell potential of COPR upon treatment. This study investigated the use of ferrous chloride alone and in combination with Portland cement to address the detoxification of Cr(VI) in COPR and the potential swell of COPR. Chromium regulatory tests, X-ray powder diffraction (XRPD) analyses and X-ray absorption near edge structure (XANES) analyses were used to assess the treatment results. The treatment results indicated that Cr(VI) concentrations for the acid pretreated micronized COPR as measured by XANES analyses were below the New Jersey Department of Environmental Protection (NJDEP) standard of 20 mg kg(-1). The Toxicity characteristic leaching procedure (TCLP) Cr concentrations for all acid pretreated samples also were reduced below the TCLP regulatory limit of 5 mg L(-1). Moreover, the TCLP Cr concentration for the acid pretreated COPR with particle size ⩽0.010 mm were less than the universal treatment standard (UTS) of 0.6 mg L(-1). The treatment appears to have destabilized all COPR potential swell causing minerals. The unconfined compressive strength (UCS) for the treated samples increased significantly upon treatment with Portland cement.

  20. Optical amplification in disordered electrooptic Tm{sup 3+} and Ho{sup 3+} codoped lanthanum-modified lead zirconate titanate ceramics and study of spectroscopy and communication between cations

    SciTech Connect

    Zhao, Hua; Zhang, Kun; Xu, Long; Sun, Fankui; Zhang, Jingwen; Chen, Xuesheng; Li, Kewen K.

    2014-02-21

    Rare earth doped electro-optic (EO) ceramics of lanthanum-modified lead zirconate titanate (PLZT) are promising in building multifunctional optical devices, by taking advantage of both EO effect and optical activity. In this work, the combination of the measured spectra of absorption and photoluminescence, the fluorescent decay, the calculated Judd-Ofelt parameters, and measured single pass gain in Tm{sup 3+}, Ho{sup 3+} codoped PLZT ceramics have marked them out as promising gain media in building electrically controllable lasers/optical amplifiers and other multifunctional devices. Optical energy storage was also observed in the optical amplification dynamics.

  1. The variability of ruthenium in chromite from chassignite and olivine-phyric shergottite meteorites: New insights into the behavior of PGE and sulfur in Martian magmatic systems

    NASA Astrophysics Data System (ADS)

    Baumgartner, Raphael J.; Fiorentini, Marco L.; Baratoux, David; Ferrière, Ludovic; Locmelis, Marek; Tomkins, Andrew; Sener, Kerim A.

    2017-02-01

    The Martian meteorites comprise mantle-derived mafic to ultramafic rocks that formed in shallow intrusions and/or lava flows. This study reports the first in situ platinum-group element data on chromite and ulvöspinel from a series of dunitic chassignites and olivine-phyric shergottites, determined using laser-ablation ICP-MS. As recent studies have shown that Ru has strongly contrasting affinities for coexisting sulfide and spinel phases, the precise in situ analysis of this element in spinel can provide important insights into the sulfide saturation history of Martian mantle-derived melts. The new data reveal distinctive differences between the two meteorite groups. Chromite from the chassignites Northwest Africa 2737 (NWA 2737) and Chassigny contained detectable concentrations of Ru (up to 160 ppb Ru) in solid solution, whereas chromite and ulvöspinel from the olivine-phyric shergottites Yamato-980459 (Y-980459), Tissint, and Dhofar 019 displayed Ru concentrations consistently below detection limit (<42 ppb). The relatively elevated Ru signatures of chromite from the chassignites suggest a Ru-rich ( 1-4 ppb) parental melt for this meteorite group, which presumably did not experience segregation of immiscible sulfide liquids over the interval of mantle melting, melt ascent, and chromite crystallization. The relatively Ru-depleted signature of chromite and ulvöspinel from the olivine-phyric shergottites may be the consequence of relatively lower Ru contents (<1 ppb) in the parental melts, and/or the presence of sulfides during the crystallization of the spinel phases. The results of this study illustrate the significance of platinum-group element in situ analysis on spinel phases to decipher the sulfide saturation history of magmatic systems.

  2. Cellulose-lanthanum hydroxide nanocomposite as a selective marker for detection of toxic copper

    NASA Astrophysics Data System (ADS)

    Marwani, Hadi M.; Lodhi, Mazhar Ullah; Khan, Sher Bahadar; Asiri, Abdullah M.

    2014-09-01

    In this current report, a simple, reliable, and rapid method based on modifying the cellulose surface by doping it with different percentages of lanthanum hydroxide (i.e., 1% La(OH)3-cellulose (LC), 5% La(OH)3-cellulose (LC2), and 10% La(OH)3-cellulose (LC3)) was proposed as a selective marker for detection of copper (Cu(II)) in aqueous medium. Surface properties of the newly modified cellulose phases were confirmed by Fourier transform infrared spectroscopy, field emission scanning electron microscope, energy dispersive X-ray spectroscopy, X-ray diffraction, and X-ray photoelectron spectroscopic analysis. The effect of pH on the adsorption of modified cellulose phases for Cu(II) was evaluated, and LC3 was found to be the most selective for Cu(II) at pH 6.0. Other parameters, influencing the maximum uptake of Cu(II) on LC3, were also investigated for a deeper mechanistic understanding of the adsorption phenomena. Results showed that the adsorption capacity for Cu(II) was improved by 211% on the LC3 phase as compared to diethylaminoethyl cellulose phase after only 2 h contact time. Adsorption isotherm data established that the adsorption process nature was monolayer with a homogeneous adsorbent surface. Results displayed that the adsorption of Cu(II) onto the LC3 phase obeyed a pseudo-second-order kinetic model. Selectivity studies toward eight metal ions, i.e., Cd(II), Co(II), Cr(III), Cr(VI), Cu(II), Fe(III), Ni(II), and Zn(II), were further performed at the optimized pH value. Based on the selectivity study, it was found that Cu(II) is highly selective toward the LC3 phase. Moreover, the efficiency of the proposed method was supported by implementing it to real environmental water samples with adequate results.

  3. Application of artificial neural network in 3D imaging with lanthanum bromide calorimeter

    NASA Astrophysics Data System (ADS)

    Gostojic, A.; Tatischeff, V.; Kiener, J.; Hamadache, C.; Karkour, N.; Linget, D.; Grave, X.; Gibelin, L.; Travers, B.; Blin, S.; Barrillon, P.

    2015-07-01

    Gamma-ray astronomy in the energy range from 0.1 up to 100 MeV holds many understudied questions connected with e.g. stellar nucleosynthesis, the active Sun, neutron stars and black holes. To access the physics behind, a significant improvement in detection sensitivity is needed compared to previous missions, e.g. CGRO and INTEGRAL. One of the promising concepts for a future gamma-ray mission is an Advanced Compton Telescope. Under the project of creating a prototype of such instrument, we study the perspectives of using a novel inorganic scintillator as a calorimeter part. Modern inorganic crystal or ceramics scintillators are constantly improving on qualities such as energy resolution and radiation hardness, and this makes them a smart choice for a new space-borne telescope. At CSNSM Orsay, we have assembled a detection module from a 5 × 5cm2 area and 1 cm thick, cerium-doped lanthanum (III) bromide (LaBr3:Ce) inorganic scintillator coupled to a 64 channel multi-anode photomultiplier. The readout of the PMT signals is carried out with the ASIC MAROC, used previously for the luminometer of the ATLAS detector (CERN). Characterization, thorough measurements with various radioactive sources, as well as, single photoelectron detection have been done. Furthermore, we made a comparison of measurements with a detailed GEANT4-based simulation which includes tracking of the optical photons. Finally, we have studied the 3D reconstruction of the first interaction point of incident gamma rays, utilizing a neural network algorithm. This spatial position resolution plays a crucial part in the future implementations and, together with the other measured properties, it makes our detector module very interesting for the next generation of space telescopes operating in the MeV range.

  4. Cellulose-lanthanum hydroxide nanocomposite as a selective marker for detection of toxic copper

    PubMed Central

    2014-01-01

    In this current report, a simple, reliable, and rapid method based on modifying the cellulose surface by doping it with different percentages of lanthanum hydroxide (i.e., 1% La(OH)3-cellulose (LC), 5% La(OH)3-cellulose (LC2), and 10% La(OH)3-cellulose (LC3)) was proposed as a selective marker for detection of copper (Cu(II)) in aqueous medium. Surface properties of the newly modified cellulose phases were confirmed by Fourier transform infrared spectroscopy, field emission scanning electron microscope, energy dispersive X-ray spectroscopy, X-ray diffraction, and X-ray photoelectron spectroscopic analysis. The effect of pH on the adsorption of modified cellulose phases for Cu(II) was evaluated, and LC3 was found to be the most selective for Cu(II) at pH 6.0. Other parameters, influencing the maximum uptake of Cu(II) on LC3, were also investigated for a deeper mechanistic understanding of the adsorption phenomena. Results showed that the adsorption capacity for Cu(II) was improved by 211% on the LC3 phase as compared to diethylaminoethyl cellulose phase after only 2 h contact time. Adsorption isotherm data established that the adsorption process nature was monolayer with a homogeneous adsorbent surface. Results displayed that the adsorption of Cu(II) onto the LC3 phase obeyed a pseudo-second-order kinetic model. Selectivity studies toward eight metal ions, i.e., Cd(II), Co(II), Cr(III), Cr(VI), Cu(II), Fe(III), Ni(II), and Zn(II), were further performed at the optimized pH value. Based on the selectivity study, it was found that Cu(II) is highly selective toward the LC3 phase. Moreover, the efficiency of the proposed method was supported by implementing it to real environmental water samples with adequate results. PMID:25258599

  5. Compositional variations in the Mesoarchean chromites of the Nuggihalli schist belt, Western Dharwar Craton (India): potential parental melts and implications for tectonic setting

    NASA Astrophysics Data System (ADS)

    Mukherjee, Ria; Mondal, Sisir K.; Rosing, Minik T.; Frei, Robert

    2010-12-01

    The chromite deposits in the Archean Nuggihalli schist belt are part of a layered ultramafic-mafic sequence within the Western Dharwar Craton of the Indian shield. The 3.1-Ga ultramafic-mafic units occur as sill-like intrusions within the volcano-sedimentary sequences of the Nuggihalli greenstone belt that are surrounded by the tonalite-trondhjemite-granodiorite (TTG) suite of rocks. The entire succession is exposed in the Tagdur mining district. The succession has been divided into the lower and the upper ultramafic units, separated by a middle gabbro unit. The ultramafic units comprise of deformed massive chromitite bodies that are hosted within chromite-bearing serpentinites. The chromitite bodies occur in the form of pods and elongated lenses (~60-500 m by ~15 m). Detailed electron microprobe studies reveal intense compositional variability of the chromite grains in silicate-rich chromitite (~50% modal chromite) and serpentinite (~2% modal chromite) throughout the entire ultramafic sequence. However, the primary composition of chromite is preserved in the massive chromitites (~60-75% modal chromite) from the Byrapur and the Bhaktarhalli mining district of the Nuggihalli schist belt. These are characterized by high Cr-ratios (Cr/(Cr + Al) = 0.78-0.86) and moderate Mg-ratios (Mg/(Mg + Fe2+) = 0.38-0.58). The compositional variability occurs due to sub-solidus re-equilibration in the accessory chromite in the serpentinite (Mg-ratio = 0.01-0.38; Cr-ratio = 0.02-0.99) and in silicate-rich chromitite (Mg-ratio = 0.06-0.48; Cr-ratio = 0.60-0.99). In the massive chromitites, the sub-solidus re-equilibration for chromite is less or absent. However, the re-equilibration is prominent in the co-existing interstitial and included olivine (Fo96-98) and pyroxene grains (Mg-numbers = 97-99). Compositional variability on the scale of a single chromite grain occurs in the form of zoning, and it is common in the accessory chromite grains in serpentinite and in the altered grains

  6. Airplane dopes and doping

    NASA Technical Reports Server (NTRS)

    Smith, W H

    1919-01-01

    Cellulose acetate and cellulose nitrate are the important constituents of airplane dopes in use at the present time, but planes were treated with other materials in the experimental stages of flying. The above compounds belong to the class of colloids and are of value because they produce a shrinking action on the fabric when drying out of solution, rendering it drum tight. Other colloids possessing the same property have been proposed and tried. In the first stages of the development of dope, however, shrinkage was not considered. The fabric was treated merely to render it waterproof. The first airplanes constructed were covered with cotton fabric stretched as tightly as possible over the winds, fuselage, etc., and flying was possible only in fine weather. The necessity of an airplane which would fly under all weather conditions at once became apparent. Then followed experiments with rubberized fabrics, fabrics treated with glue rendered insoluble by formaldehyde or bichromate, fabrics treated with drying and nondrying oils, shellac, casein, etc. It was found that fabrics treated as above lost their tension in damp weather, and the oil from the motor penetrated the proofing material and weakened the fabric. For the most part the film of material lacked durability. Cellulose nitrate lacquers, however were found to be more satisfactory under varying weather conditions, added less weight to the planes, and were easily applied. On the other hand, they were highly inflammable, and oil from the motor penetrated the film of cellulose nitrate, causing the tension of the fabric to be relaxed.

  7. Morphology-controlled nonaqueous synthesis of anisotropic lanthanum hydroxide nanoparticles

    SciTech Connect

    Djerdj, Igor; Garnweitner, Georg; Sheng Su, Dang; Niederberger, Markus

    2007-07-15

    The preparation of lanthanum hydroxide and manganese oxide nanoparticles is presented, based on a nonaqueous sol-gel process involving the reaction of La(OiPr){sub 3} and KMnO{sub 4} with organic solvents such as benzyl alcohol, 2-butanone and a 1:1 vol. mixture thereof. The lanthanum manganese oxide system is highly complex and surprising results with respect to product composition and morphology were obtained. In dependence of the reaction parameters, the La(OH){sub 3} nanoparticles undergo a shape transformation from short nanorods with an average aspect ratio of 2.1 to micron-sized nanofibers (average aspect ratio is more than 59.5). Although not directly involved, KMnO{sub 4} plays a crucial role in determining the particle morphology of La(OH){sub 3}. The reason lies in the fact that KMnO{sub 4} is able to oxidize the benzyl alcohol to benzoic acid, which presumably induces the anisotropic particle growth in [0 0 1] direction upon preferential coordination to the {+-}(1 0 0), {+-}(0 1 0) and {+-}(-110) crystal facets. By adjusting the molar La(OiPr){sub 3}-to-KMnO{sub 4} ratio as well as by using the appropriate solvent mixture it is possible to tailor the morphology, phase purity and microstructure of the La(OH){sub 3} nanoparticles. Postsynthetic thermal treatment of the sample containing La(OH){sub 3} nanofibers and {beta}-MnOOH nanoparticles at the temperature of 800 deg. C for 8 h yielded polyhedral LaMnO{sub 3} and worm-like La{sub 2}O{sub 3} nanoparticles as final products. - Graphical abstract: Lanthanum hydroxide nanoparticles are synthesized based on a nonaqueous sol-gel process involving the reaction of La(OiPr){sub 3} and KMnO{sub 4} with organic solvents such as benzyl alcohol, 2-butanone and a 1:1 vol. mixture thereof. In dependence of the reaction parameters, the La(OH){sub 3} nanoparticles undergo a shape transformation from short nanorods to micron-sized nanofibers.

  8. Thermodynamic stability of perovskite and lanthanum nickelate-type cathode materials for solid oxide fuel cells

    NASA Astrophysics Data System (ADS)

    Cetin, Deniz

    The need for cleaner and more efficient alternative energy sources is becoming urgent as concerns mount about climate change wrought by greenhouse gas emissions. Solid oxide fuel cells (SOFCs) are one of the most efficient options if the goal is to reduce emissions while still operating on fossil energy resources. One of the foremost problems in SOFCs that causes efficiency loss is the polarization resistance associated with the oxygen reduction reaction(ORR) at the cathodes. Hence, improving the cathode design will greatly enhance the overall performance of SOFCs. Lanthanum nickelate, La2NiO4+delta (LNO), is a mixed ionic and electronic conductor that has competitive surface oxygen exchange and transport properties and excellent electrical conductivity compared to perovskite-type oxides. This makes it an excellent candidate for solid oxide fuel cell (SOFC) applications. It has been previously shown that composites of LNO with Sm0.2Ce0.8O2-delta (SDC20) as cathode materials lead to higher performance than standalone LNO. However, in contact with lanthanide-doped ceria, LNO decomposes resulting in free NiO and ceria with higher lanthanide dopant concentration. In this study, the aforementioned instability of LNO has been addressed by compositional tailoring of LNO: lanthanide doped ceria (LnxCe 1-xO2,LnDC)composite. By increasing the lanthanide dopant concentration in the ceria phase close to its solubility limit, the LNO phase has been stabilized in the LNO:LnDC composites. Electrical conductivity of the composites as a function of LNO volume fraction and temperature has been measured, and analyzed using a resistive network model which allows the identification of a percolation threshold for the LNO phase. The thermomechanical compatibility of these composites has been investigated with SOFC systems through measurement of the coefficients of thermal expansion. LNO:LDC40 composites containing LNO lower than 50 vol%and higher than 40 vol% were identified as being

  9. Lanthanum Probe Studies of Cellular Pathophysiology Induced by Hypoxia in Isolated Cardiac Muscle

    PubMed Central

    Burton, Karen P.; Hagler, Herbert K.; Templeton, Gordon H.; Willerson, James T.; Buja, L. Maximilian

    1977-01-01

    This study was undertaken to evaluate directly the relationship between evolution of irreversible myocardial injury induced by hypoxia in an isolated papillary muscle preparation and the development of pathophysiological alterations related to severely impaired membrane function. An ionic lanthanum probe technique was employed as a cytochemical marker to monitor the progression of cellular injury, and data from this cytologic technique were correlated with ultrastructure and measurements of contractile parameters in a total of 67 muscles subjected to control conditions or to graded intervals of hypoxia with or without reoxygenation. Marked depression of developed tension and rate of tension development occurred after 30 min of hypoxia. Contractile function showed significant recovery with reoxygenation after 1 h and 15 min of hypoxia but remained depressed when reoxygenation was provided after 2 or 3 h of hypoxia. Examination by transmission and analytical electron microscopy (energy dispersive X-ray microanalysis) revealed lanthanum deposition only in extracellular regions of control muscles and muscles subjected to 30 min of hypoxia. After hypoxic intervals of over 1 h, abnormal intracytoplasmic and intramitochondrial localization of lanthanum were detected. After 1 h and 15 min of hypoxia, abnormal intracellular lanthanum accumulation was associated with only minimal ultrastructural evidence of injury; muscle provided reoxygenation after 1 h and 15 min of hypoxia showed improved ultrastructure and did not exhibit intracellular lanthanum deposits upon exposure to lanthanum during the reoxygenation period. After 2 to 3 h of hypoxia, abnormal intracellular lanthanum accumulation was associated with ultrastructural evidence of severe muscle injury which persisted after reoxygenation. Thus, the data support the conclusion that cellular and membrane alterations responsible for abnormal intracellular lanthanum deposition precede the development of irreversible injury

  10. Density Optimization of Lithium Lanthanum Titanate Ceramics for Lightweight Lithium-Air Batteries

    DTIC Science & Technology

    2014-11-01

    Thangadurai V, Weppner W. Lithium lanthanum titanates: a review. Chemistry of Materials. 2003;15:3974–3990. 4. Knauth P. Inorganic solid Li ion conductors...an overview. Solid State Ionics. 2009;180:911–916. 5. Ban CW, Choi GM. The effect of sintering on the grain boundary conductivity of lithium ...lanthanum titanates. Solid State Ionics. 2001;140:285–292. 6. Inada R, Kimura K, Kusakabe K, Tojo T, Sakurai Y. Synthesis and lithium -ion conductivity

  11. Environmental status of groundwater affected by chromite ore processing residue (COPR) dumpsites during pre-monsoon and monsoon seasons.

    PubMed

    Matern, Katrin; Weigand, Harald; Singh, Abhas; Mansfeldt, Tim

    2017-02-01

    Chromite ore processing residue (COPR) is generated by the roasting of chromite ores for the extraction of chromium. Leaching of carcinogenic hexavalent chromium (Cr(VI)) from COPR dumpsites and contamination of groundwater is a key environmental risk. The objective of the study was to evaluate Cr(VI) contamination in groundwater in the vicinity of three COPR disposal sites in Uttar Pradesh, India, in the pre-monsoon and monsoon seasons. Groundwater samples (n = 57 pre-monsoon, n = 70 monsoon) were taken in 2014 and analyzed for Cr(VI) and relevant hydrochemical parameters. The site-specific ranges of Cr(VI) concentrations in groundwater were <0.005 to 34.8 mg L(-1) (Rania), <0.005 to 115 mg L(-1) (Chhiwali), and <0.005 to 2.0 mg L(-1) (Godhrauli). Maximum levels of Cr(VI) were found close to the COPR dumpsites and significantly exceeded safe drinking water limits (0.05 mg L(-1)). No significant dependence of Cr(VI) concentration on monsoons was observed.

  12. Lanthanum carbonate: a review of its use in lowering serum phosphate in patients with end-stage renal disease.

    PubMed

    Curran, Monique P; Robinson, Dean M

    2009-11-12

    Orally administered lanthanum carbonate (Fosrenol) dissociates in the acid environment of the upper gastrointestinal tract to release the cation lanthanum, which then binds dietary phosphate. Lanthanum carbonate was effective in reducing levels of serum phosphate and serum calcium x phosphate product and then maintaining these levels within target ranges for up to 6 years in adult patients with end-stage renal disease (ESRD) on haemodialysis or peritoneal dialysis. The reduction in serum phosphate levels with lanthanum carbonate was generally similar to that with calcium carbonate or sevelamer hydrochloride. This agent was generally well tolerated, with the most frequently reported adverse events being gastrointestinal in nature and occurring at a similar rate to that with calcium carbonate. However, lanthanum carbonate was associated with fewer episodes of hypercalcaemia than calcium carbonate. Overall, lanthanum carbonate is a valuable option for the reduction of serum phosphate levels in patients with ESRD on haemodialysis or peritoneal dialysis.

  13. Synthesis and characterization of strontium-lanthanum apatites

    SciTech Connect

    Boughzala, K.; Salem, E. Ben; Chrifa, A. Ben; Gaudin, E.; Bouzouita, K. . E-mail: khaled.bouzouita@ipeim.rnu.tn

    2007-07-03

    Two series of strontium-lanthanum apatites, Sr{sub 10-x}La {sub x}(PO{sub 4}){sub 6-x}(SiO{sub 4}) {sub x}F{sub 2} and Sr{sub 10-x}La {sub x}(PO{sub 4}){sub 6-x}(SiO{sub 4}) {sub x}O with 0 {<=} x {<=} 6, were synthesized by solid state reaction in the temperature range of 1200-1400 deg. C. The obtained materials were characterized by powder X-ray diffraction, infrared absorption spectroscopy and solid {sup 31}P Nuclear Magnetic Resonance. Pure solid solutions were obtained within a limited range of unsubstituted phosphate and silicate apatites. A variation of the lattice parameters was observed, with an increase of a and a decrease of c parameters, related to the radius of the corresponding substituted ions.

  14. Fabrication of calcium lanthanum sulfide ceramic by carbonate coprecipitating method

    SciTech Connect

    Tsai, M.S.; Hon, M.H. . Dept. of Materials Science and Engineering)

    1995-03-01

    Translucent CLS (calcium lanthanum sulfide) pellets were formed by the carbonate coprecipitation method, CS[sub 2] sulfurization, and hot press sintering. For a La/Ca = 2.5 pellet with 1.3 mm in thickness, the transmittance at 13 [mu]m is about 25% after sintering at 1,150 C for 30 minutes and resulfurizing at 950 C for 1 hour. For a La/Ca = 15 pellet with 0.9 mm in thickness the IR transmittance is about 51% at 13 [mu]m after sintering at 1,050 C for 2 hours and resulfurizing at 950 C for 1 hour. Beta-La[sub 2]S[sub 3] is present as a second phase after sintering at 1,150 C for 30 minutes. After resulfurization, the second phase disappears for the La/Ca = 2.5 pellet, but still exists in the La/Ca = 15 pellet.

  15. Phase separation of lanthanum hydride under high pressure

    NASA Astrophysics Data System (ADS)

    Machida, A.; Watanuki, T.; Kawana, D.; Aoki, K.

    2011-02-01

    Structural change of lanthanum dihydride LaH2.3, which has a face-centered-cubic (fcc) metal lattice with tetrahedral interstitial sites fully occupied with hydrogen atoms and partially occupied octahedral sites, has been investigated at high pressures up to 20 GPa at ambient temperature by synchrotron radiation x-ray diffraction. Additional Bragg reflections appear just on higher angle sides of the original ones at ~11 GPa and their peak intensities increase gradually on further compression. The coexistence state of two fcc metal lattices thus observed above 11 GPa is interpreted in terms of phase separation or disproportionation reaction from the dihydride toward a solid solution and trihydride states, in both of which the octahedral interstitial sites are partially occupied with hydrogen atoms. A gradual distortion from the cubic to a tetragonal lattice is observed prior to the phase separation. The coexistence phase goes back to the dihydride fcc phase via the lattice distorted phase with decreasing pressure.

  16. Recent advances of lanthanum-based perovskite oxides for catalysis

    SciTech Connect

    Zhu, Huiyuan; Zhang, Pengfei; Dai, Sheng

    2015-09-21

    There is a need to reduce the use of noble metal elements especially in the field of catalysis, where noble metals are ubiquitously applied. To this end, perovskite oxides, an important class of mixed oxide, have been attracting increasing attention for decades as potential replacements. Benefiting from the extraordinary tunability of their compositions and structures, perovskite oxides can be rationally tailored and equipped with targeted physical and chemical properties e.g. redox behavior, oxygen mobility, and ion conductivity for enhanced catalysis. Recently, the development of highly efficient perovskite oxide catalysts has been extensively studied. This review article summarizes the recent development of lanthanum-based perovskite oxides as advanced catalysts for both energy conversion applications and traditional heterogeneous reactions.

  17. Recent advances of lanthanum-based perovskite oxides for catalysis

    DOE PAGES

    Zhu, Huiyuan; Zhang, Pengfei; Dai, Sheng

    2015-09-21

    There is a need to reduce the use of noble metal elements especially in the field of catalysis, where noble metals are ubiquitously applied. To this end, perovskite oxides, an important class of mixed oxide, have been attracting increasing attention for decades as potential replacements. Benefiting from the extraordinary tunability of their compositions and structures, perovskite oxides can be rationally tailored and equipped with targeted physical and chemical properties e.g. redox behavior, oxygen mobility, and ion conductivity for enhanced catalysis. Recently, the development of highly efficient perovskite oxide catalysts has been extensively studied. This review article summarizes the recent developmentmore » of lanthanum-based perovskite oxides as advanced catalysts for both energy conversion applications and traditional heterogeneous reactions.« less

  18. The management of hyperphosphatemia by lanthanum carbonate in chronic kidney disease patients.

    PubMed

    Shigematsu, Takashi; Nakashima, Yuri; Ohya, Masaki; Tatsuta, Koichi; Koreeda, Daisuke; Yoshimoto, Wataru; Yamanaka, Shintaro; Sakaguchi, Toshifumi; Hanba, Yoshiyuki; Mima, Toru; Negi, Shigeo

    2012-01-01

    Hyperphosphatemia has been shown to be involved not only in the onset and progression of secondary hyperparathyroidism but also in vascular calcification. In addition, it influences the clinical course of patients with chronic kidney disease. Phosphate (Pi) binder is required in the management of hyperparaphosphatemia, because dietary Pi restriction and Pi removal by hemodialysis alone are insufficient. Lanthanum carbonate, a powerful Pi binder, has a similar effect to aluminum hydroxide in reducing serum Pi levels. As it is excreted via the liver, lanthanum carbonate has an advantage in patients with renal failure. The effect of lanthanum carbonate on serum Pi levels is almost two times higher than that of calcium (Ca) carbonate, which is commonly used. Lanthanum carbonate and Ca carbonate have an additive effect. Worldwide, there is 6 years worth of clinical treatment data on lanthanum carbonate; however, we have 3 years of clinical use in Japanese patients with hyperphosphatemia. No serious side effects have been reported. However, the most important concern is bone toxicity, which has been observed with use of aluminum hydroxide. For this study, clinical research involved analysis of bone biopsies. Although osteomalacia is the most noticeable side effect, this was not observed. Both the high- and the low-turnover bone disease concentrated into a normal bone turnover state. However, as the authors have less than 10 years' clinical experience with lanthanum carbonate, patients should be monitored carefully. In addition, it is necessary to demonstrate whether potent treatment effects on hyperphosphatemia improve the long-term outcome.

  19. Infrared spectra of oxygen-rich yttrium and lanthanum dioxygen/ozonide complexes in solid argon.

    PubMed

    Gong, Yu; Ding, Chuanfan; Zhou, Mingfei

    2009-07-30

    The reactions of yttrium and lanthanum atoms with O(2) have been reinvestigated using matrix isolation infrared spectroscopy and theoretical calculations. The ground-state yttrium and lanthanum atoms react with O(2) to produce the inserted yttrium and lanthanum dioxide molecules as the initial products. The yttrium dioxide molecule interacts spontaneously with additional O(2) molecules to form the oxygen-rich OY(eta(2)-O(3)) complex and possibly the (eta(2)-O(2))Y(eta(2)-O(3))(2) complexes upon sample annealing, which can be regarded as the side-on bonded yttrium monoxide ozonide complex and the superoxo yttrium bisozonide complex, respectively. Visible irradiation induces the isomerization of the OY(eta(2)-O(3)) complex to the superoxo yttrium peroxide Y(eta(2)-O(2))(2) isomer, in which both the superoxo and peroxo ligands are side-on bonded to the yttrium center. The lanthanum dioxide molecule reacts with additional O(2) molecules to form the lanthanum dioxide-dioxygen complex with planar C(2v) symmetry, which rearranges to the lanthanum monoxide ozonide complex, OLa(eta(2)-O(3)), under near-infrared excitation.

  20. Studies on gel-grown pure and strontium-modified lanthanum tartrate crystals

    NASA Astrophysics Data System (ADS)

    Firdous, A.; Quasim, I.; Ahmad, M. M.; Kotru, P. N.

    2009-07-01

    Crystals of pure and strontium-modified lanthanum tartrate bearing composition (La) 1-x(Sr) xC 4H 4O 6· nH 2O (where x=0, 0.04, 0.10, 0.15; n=5,5,6,8) were obtained using gel method. The materials were studied using CH analysis, X-ray powder diffraction, FTIR, EDAX and thermoanalytical techniques. X-ray powder diffraction results analyzed by using suitable software suggest that while unmodified lanthanum tartrate has a monoclinic structure with the space group P 21, the entry of strontium into its lattice changes the system to orthorhombic with the space group P 2121. The unit cell volume is observed to decrease with increase in the concentration of strontium in lanthanum tartrate. Thermal analysis suggests that pure lanthanum tartrate starts decomposing at 41.31 °C whereas the strontium-modified lanthanum tartrate brings about better thermal stability which increases with an increase in strontium concentration. The percentage weight loss calculations from the thermogram supplemented by EDAX, CH analysis and FTIR spectroscopy suggest that both unmodified and strontium-modified lanthanum tartrate spherulitic crystals contain water of hydration; the amount of water of hydration being different for crystals with different content of strontium.

  1. Electronic states and spin-orbit splitting of lanthanum dimer

    NASA Astrophysics Data System (ADS)

    Liu, Yang; Wu, Lu; Zhang, Chang-Hua; Krasnokutski, Serge A.; Yang, Dong-Sheng

    2011-07-01

    Lanthanum dimer (La2) was studied by mass-analyzed threshold ionization (MATI) spectroscopy and a series of multi-configuration ab initio calculations. The MATI spectrum exhibits three band systems originating from ionization of the neutral ground electronic state, and each system shows vibrational frequencies of the neutral molecule and singly charged cation. The three ionization processes are La2+ (a2∑g+) ← La2 (X1∑g+), La2+ (b2Π3/2, u) ← La2 (X1∑g+), and La2+ (b2Π1/2, u) ← La2 (X1∑g+), with the ionization energies of 39 046, 40 314, and 40 864 cm-1, respectively. The vibrational frequency of the X1Σg+ state is 207 cm-1, and those of the a2Σg+, b2Π3/2, u and b2Π1/2, u are 235.7, 242.2, and 240 cm-1. While X1Σg+ is the ground state of the neutral molecule, a2Σg+ and b2Πu are calculated to be the excited states of the cation. The spin-orbit splitting in the b2Πu ion is 550 cm-1. An X4Σg- state of La2+ was predicted by theory, but not observed by the experiment. The determination of a singlet ground state of La2 shows that lanthanum behaves differently from scandium and yttrium.

  2. Structural, magnetic and catalytic properties of cobalt chromite obtained through precursor method

    SciTech Connect

    Gingasu, Dana; Mindru, Ioana; Culita, Daniela C.; Patron, Luminita; Calderon-Moreno, Jose Maria; Osiceanu, Petre; Preda, Silviu; Oprea, Ovidiu; Parvulescu, Viorica; Teodorescu, Valentin; Walsh, James P.S.

    2015-02-15

    Highlights: • CoCr{sub 2}O{sub 4} was synthesized through the tartarate and gluconate precursor routes. • Both routes led to the formation of the single-phase CoCr{sub 2}O{sub 4}. • The crystallite size was in the range of 14–21 nm. • CoCr{sub 2}O{sub 4} samples presented ferrimagnetic ordering below Currie temperature T{sub c} = 97 K. • CoCr{sub 2}O{sub 4} samples presented catalytic performance in the total oxidation of CH{sub 4}. - Abstract: Cobalt chromite (CoCr{sub 2}O{sub 4}) was synthesized through the precursor method. The precursors: (NH{sub 4}){sub 3}[CoCr{sub 2}(C{sub 4}O{sub 6}H{sub 4}){sub 4}(OH){sub 3}]·4H{sub 2}O, (NH{sub 4}){sub 3}[CoCr{sub 2}(C{sub 6}O{sub 7}H{sub 10}){sub 4}(C{sub 6}O{sub 7}H{sub 9})]·5H{sub 2}O were characterized by elemental chemical analysis, infrared (IR) and ultraviolet–visible (UV–vis) spectroscopy, and thermal analysis. The final oxides were characterized by X-ray diffraction (XRD), scanning and transmission electron microscopy (SEM/TEM), UV–vis, IR, Raman spectroscopy (RS), magnetic measurements, N{sub 2} adsorption–desorption analyses and X-ray photoelectron spectroscopy (XPS). XRD confirmed the cubic CoCr{sub 2}O{sub 4} phase only and determined average crystallite sizes between 14 and 21 nm. Electron microscopy revealed morphology corresponding to the complete crystallization into cubic CoCr{sub 2}O{sub 4}. All the samples presented ferrimagnetic ordering below the Currie temperature (T{sub c}), and a phase transition at T{sub s} ∼26 K attributed to the onset of long-range spiral magnetic order. The CoCr{sub 2}O{sub 4} nanoparticles generated through the gluconate route following calcination at 700 °C for 1 h were found to have the best catalytic activity in the total oxidation of methane.

  3. In Situ Reduction of Hexavalent Chromium in Alkaline Soils Enriched with Chromite Ore Processing Residue.

    PubMed

    Higgins, Thomas E; Halloran, Amy R; Dobbins, Maribeth E; Pittignano, Alex J

    1998-11-01

    In investigating chromium sites in New Jersey, it has been observed that an organic-rich 0.5- to 4-foot-thick layer of decayed vegetation (locally known as "meadowmat") underlying the chromium-containing material acts as a natural barrier to the migration of Cr(VI). The groundwater in a sand layer directly beneath the meadowmat has been shown to contain low or nondetectable levels of chromium. The meadowmat is under highly reduced conditions due to bacterial activity associated with the organic material. Based on the observed ability of the meadowmat to reduce Cr(VI) to Cr(III), the feasibility of in situ reduction of Cr(VI) to Cr(III) at chromite ore processing residue (COPR) sites was investigated in biologically-active, laboratory-scale test columns. COPR typically has a high pH (in excess of 12) and may contain total chromium concentrations as high as 70,000 mg/kg. Experimental results demonstrated that the addition of a mineral acid (to lower the pH to between 7.0 and 9.5) and a bacteria-rich organic substrate (fresh manure) resulted in the reduction of Cr(VI) to the less toxic and less mobile trivalent form. Pore water Cr(VI) was reduced from approximately 800 mg/L to less than 0.05 mg/L over a period of eight months. This is less than the U.S. Environmental Protection Agency's (EPA) Maximum Contaminant Level (MCL) for chromium in drinking water of 0.1 mg/L. Solid phase Cr(VI) concentrations decreased from approximately 2,000 mg/kg to less than 10 mg/kg in the columns over a period of 11 months while the total chromium concentrations remained unchanged. Toxicity Characteristic Leaching Procedure (TCLP) extract from the treated columns met the regulatory limit of 5 mg/L of Cr, whereas the untreated samples had TCLP extract concentrations greater than 40 mg/L. This study demonstrated the potential applicability of in situ reduction to soils contaminated with Cr(VI) by adjusting the pH to between 7.0 and 9.5 and mixing in a bacteria-rich organic substrate.

  4. In situ reduction of hexavalent chromium in alkaline soils enriched with chromite ore processing residue

    PubMed

    Higgins; Halloran; Dobbins; Pittignano

    1998-11-01

    In investigating chromium sites in New Jersey, it has been observed that an organic-rich 0.5- to 4-foot-thick layer of decayed vegetation (locally known as "meadowmat") underlying the chromium-containing material acts as a natural barrier to the migration of Cr(VI). The groundwater in a sand layer directly beneath the meadowmat has been shown to contain low or nondetectable levels of chromium. The meadowmat is under highly reduced conditions due to bacterial activity associated with the organic material. Based on the observed ability of the meadowmat to reduce Cr(VI) to Cr(III), the feasibility of in situ reduction of Cr(VI) to Cr(III) at chromite ore processing residue (COPR) sites was investigated in biologically-active, laboratory-scale test columns. COPR typically has a high pH (in excess of 12) and may contain total chromium concentrations as high as 70,000 mg/kg. Experimental results demonstrated that the addition of a mineral acid (to lower the pH to between 7.0 and 9.5) and a bacteria-rich organic substrate (fresh manure) resulted in the reduction of Cr(VI) to the less toxic and less mobile trivalent form. Pore water Cr(VI) was reduced from approximately 800 mg/L to less than 0.05 mg/L over a period of eight months. This is less than the U.S. Environmental Protection Agency's (EPA) Maximum Contaminant Level (MCL) for chromium in drinking water of 0.1 mg/L. Solid phase Cr(VI) concentrations decreased from approximately 2,000 mg/kg to less than 10 mg/kg in the columns over a period of 11 months while the total chromium concentrations remained unchanged. Toxicity Characteristic Leaching Procedure (TCLP) extract from the treated columns met the regulatory limit of 5 mg/L of Cr, whereas the untreated samples had TCLP extract concentrations greater than 40 mg/L. This study demonstrated the potential applicability of in situ reduction to soils contaminated with Cr(VI) by adjusting the pH to between 7.0 and 9.5 and mixing in a bacteria-rich organic substrate.

  5. TREATMENT OF HEXAVALENT CHROMIUM IN CHROMITE ORE PROCESSING SOLID WASTE USING A MIXED REDUCTANT SOLUTION OF FERROUS SULFATE AND SODIUM DITHIONITE

    EPA Science Inventory

    We developed a method for disseminating ferrous iron in the subsurface to enhance chemical reduction of hexavalent chromium (Cr(VI)) in a chromite ore processing solid waste derived from the production of ferrochrome alloy. The method utilizes ferrous sulfate (FeSO4) in combinati...

  6. Stability of solid oxide fuel cell materials

    SciTech Connect

    Armstrong, T.R.; Bates, J.L.; Coffey, G.W.; Pederson, L.R.

    1996-08-01

    Chromite interconnection materials in an SOFC are exposed to both highly oxidizing conditions at the cathode and to highly reducing conditions at the anode. Because such conditions could lead to component failure, the authors have evaluated thermal, electrical, chemical, and structural stabilities of these materials as a function of temperature and oxygen partial pressure. The crystal lattice of the chromites was shown to expand for oxygen partial pressures smaller than 10{sup {minus}10} atm, which could lead to cracking and debonding in an SOFC. Highly substituted lanthanum chromite compositions were the most susceptible to lattice expansion; yttrium chromites showed better dimensional stability by more than a factor of two. New chromite compositions were developed that showed little tendency for lattice expansion under strongly reducing conditions, yet provided a good thermal expansion match to other fuel cell components. Use of these new chromite interconnect compositions should improve long-term SOFC performance, particularly for planar cell configurations. Thermodynamic properties of substituted lanthanum manganite cathode compositions have been determined through measurement of electromotive force as a function of temperature. Critical oxygen decomposition pressures for Sr and Ca-substituted lanthanum manganites were established using cells based on a zirconia electrolyte. Strontium oxide and calcium oxide activities in a lanthanum manganite matrix were determined using cells based on strontium fluoride and calcium fluoride electrolytes, respectively. The compositional range of single-phase behavior of these ABO{sub 3}-type perovskites was established as a function of A/B cation ratios and the extent of acceptor doping. Before this work, very little thermodynamic information was in existence for substituted manganite compositions. Such information is needed to predict the long-term stability of solid oxide fuel cell assemblies.

  7. Platinum-group elements in alpine-type ultramafic rocks and related chromite ores of the main ophiolite belt of the Urals

    NASA Astrophysics Data System (ADS)

    Volchenko, Yu. A.; Koroteev, V. A.; Neustroeva, I. I.

    2009-04-01

    On the basis of a representative collection of ultramafic rocks and chromite ores and a series of technological samples from the largest (Central and Western) deposits in the Rai-Iz massif of the Polar Urals and the Almaz-Zhemchuzhina and Poiskovy deposits in the Kempirsai massif of the southern Urals, the distribution and speciation of platinum-group elements (PGE) in various type sections of mafic-ultramafic massifs of the Main ophiolite belt of the Urals have been studied. Spectral-chemical and spectrophotometric analyses were carried out to estimate PGE in 700 samples of ultramafic rocks and chromite ores; 400 analyses of minerals from rocks, ores, and concentrates and 100 analyses of PGE minerals (PGM) in chromite ores and concentrates were performed using an electron microprobe. Near-chondritic and nonchondritic PGE patterns in chromitebearing sections have been identified. PGE mineralization has been established to occur in chromite ore from all parts of the mafic-ultramafic massifs in the Main ophiolite belt of the Urals. The PGE deposits and occurrences discovered therein are attributed to four types (Kraka, Kempirsai, Nurali-Upper Neiva, and Shandasha), which are different in mode of geological occurrence, geochemical specialization, and placer-forming capability. Fluid-bearing minerals of the pargasite-edenite series have been identified for the first time in the matrix of chromite ore of the Kempirsai massif (the Almaz-Zhemchuzhina deposit) and Voikar-Syn’ya massif (the Kershor deposit). The PGE grade in various types of chromite ore ranges from 0.1-0.2 to 1-2 g/t or higher. According to technological sampling, the average PGE grade in the largest deposits of the southeastern ore field of the Kempirsai massif is 0.5-0.7 g/t. Due to the occurrence of most PGE as PGM 10-100 mm in size and the proved feasibility of their recovery into nickel alloys, chromites of the Kempirsai massif can be considered a complex ore with elevated and locally high Os, Ir

  8. The Effect of Chromite Slag as a Binder Agent on Stress-Strain Behaviour of Cemented Tailing Backfill in Compression, a Case Study: Faryab Chromite Mine / Wpływ dodatku żużla zawierającego spoiwo w postaci chromitu na wytrzymałość na ściskanie materiału podsadzkowego zawierającego odpady pogórnicze z dodatkiem cementu. studium przypadku: kopalnia chromitu (żelaziaka chromowego) w faryab

    NASA Astrophysics Data System (ADS)

    Dehghan, Saeed; Shahriar, Koroush; Maarefvand, Parviz; Goshtasbi, Kamran

    2013-03-01

    Due to improving the environmental aspect and reduce the backfilling cost, the Faryab mine carry out researches into the replacement of cement by chromite slag. The test samples consisted of tailing from the washing plant of Faryab mine and different binders such as Portland cement, Pozzolanic cement and different combinations of Portland cement with chromite slag. The chromite slag produced by Ferrochromite refinery plant of this mine. The purpose of this paper is to analyze the findings from extensive laboratory test programs carried out to determine the effects of chromite slag on mechanical properties of cemented tailing backfills (CTB). The results show that chromite slag improves the mechanical properties of CTB samples. Also, the results indicate that chromite slag can be used as a replaceable material with cement and reduced 2-3% consumption of cement in 1 m3 of backfill mixes. In addition, improving the environmental conditions can be achieved by reducing the cement content and moving tailing and chromite slag to underground stopes.

  9. Large Electrocaloric Effect in Relaxor Ferroelectric and Antiferroelectric Lanthanum Doped Lead Zirconate Titanate Ceramics.

    PubMed

    Lu, Biao; Li, Peilian; Tang, Zhenhua; Yao, Yingbang; Gao, Xingsen; Kleemann, Wolfgang; Lu, Sheng-Guo

    2017-03-27

    Both relaxor ferroelectric and antiferroelectric materials can individually demonstrate large electrocaloric effects (ECE). However, in order to further enhance the ECE it is crucial to find a material system, which can exhibit simultaneously both relaxor ferroelectric and antiferroelectric properties, or easily convert from one into another in terms of the compositional tailoring. Here we report on a system, in which the structure can readily change from antiferroelectric into relaxor ferroelectric and vice versa. To this end relaxor ferroelectric Pb0.89La0.11(Zr0.7Ti0.3)0.9725O3 and antiferroelectric Pb0.93La0.07(Zr0.82Ti0.18)0.9825O3 ceramics were designed near the antiferroelectric-ferroelectric phase boundary line in the La2O3-PbZrO3-PbTiO3 phase diagram. Conventional solid state reaction processing was used to prepare the two compositions. The ECE properties were deduced from Maxwell relations and Landau-Ginzburg-Devonshire (LGD) phenomenological theory, respectively, and also directly controlled by a computer and measured by thermometry. Large electrocaloric efficiencies were obtained and comparable with the results calculated via the phenomenological theory. Results show great potential in achieving large cooling power as refrigerants.

  10. Preparation and laser performance of Nd-doped yttrium lanthanum oxide transparent ceramic

    NASA Astrophysics Data System (ADS)

    Yang, Qiuhong; Lu, Shenzhou; Zhang, Bin; Zhang, Haojia; Zhou, Jun; Yuan, Zhijun; Qi, Yunfeng; Lou, Qihong

    2011-03-01

    1.5 at.% Nd:Y 1.8La 0.2O 3 transparent ceramic was fabricated by a solid-state reaction method and sintered at 1650-1700 °C for 40-50 h under H 2 atmosphere. The spectroscopic properties were investigated at room temperature. The transparent ceramic has excellent spectroscopic properties, with the absorption cross section of 1.50 × 10 -20 cm 2 and broad full width at half maximum (FWHM) of about 8 nm at LD wavelength 806 nm, the emission cross section of 2.03 × 10 -20 cm 2 at 1079 nm, and the decay lifetime of 200 μs. Laser performance was carried out using an uncoated Nd:Y 1.8La 0.2O 3 ceramic plate under laser diode end-pumping without any water cooling device. The room temperature thermal conductivity of this ceramic is 6.20 W/mK. For Nd:Y 1.8La 0.2O 3 ceramic laser, a maximum output power of 62 mW was obtained at 1079 nm under a 808 nm diode pump.

  11. Fabrication and spectral properties of Nd 3+-doped yttrium lanthanum oxide transparent ceramics

    NASA Astrophysics Data System (ADS)

    Hu, Xiaoman; Yang, Qiuhong; Dou, Chuanguo; Xu, Jun; Zhou, Hongxu

    2008-06-01

    Transparent 1 at% Nd3+:Y1.9La0.1O3 ceramics were fabricated with nanopowders prepared by carbonate coprecipitation method. The powder compacts were sintered in H2 atmosphere at 1550 °C for 30 h. The Nd3+:Y1.9La0.1O3 ceramics display uniform grains of about 50 μm and high transparency. The highest transmittance of the ceramics reaches 67%. The strongest absorption peak is in the wavelength of 820 nm with absorption cross section of 2.48 × 10-20 cm2. The absorption is still high at LD wavelength 806 nm with absorption cross section of 1.78 × 10-20 cm2 and broad full width at half maximum (FWHM) of about 6.3 nm. The strongest emission peak was centered at 1078 nm with large stimulated emission cross section of 9.63 × 10-20 cm2 and broad FWHM of about 7.8 nm. The broad absorption and emission bandwidth of Nd3+:Y1.9La0.1O3 transparent ceramics are favorable to achieve the miniaturized LD pumping apparatus and ultrashort modelocked pulse laser output, respectively.

  12. Interplay Between Structural, Jahn-Teller, and Magnetic States of Slightly Doped Lanthanum Manganites

    NASA Astrophysics Data System (ADS)

    Golenishchev-Kutuzov, V. A.; Golenishchev-Kutuzov, A. V.; Kalimullin, R. I.; Semennikov, A. V.

    2016-12-01

    By combining the results of elastic moduli, electrical resistivity, and magnetization measurements for La_{1-x}SrxMnO3 ( x = 0.125, x = 0.15, and x = 0.175), we have constructed a phase diagram that describes the structural, magnetic, transport properties and the relationships among them as a function of the composition and temperature (140-340 K). The local, intermediate, and cooperative Jahn-Teller distortions of the octahedral structural units MnO6 have been studied. It is common for these distortions to be observed using probes of intermediate structures (domains or super-cells), but they are absent in the averaged crystallographic structure. In the cooperative Jahn-Teller distorted phase, the macroscopic sample length is temperature dependent. We presume that the structural transitions from the cooperative Jahn-Teller phase to the charge ordering phase at low temperatures (150 and 180 K at x = 0.125 and x = 0.15) are due to the increase in the spontaneous magnetization with the conservation of the local deformations of separate octahedra. The agreement between the types of the orbital ordering and the local, intermediate, and Jahn-Teller cooperative distortions of octahedra was established.

  13. Large Electrocaloric Effect in Relaxor Ferroelectric and Antiferroelectric Lanthanum Doped Lead Zirconate Titanate Ceramics

    PubMed Central

    Lu, Biao; Li, Peilian; Tang, Zhenhua; Yao, Yingbang; Gao, Xingsen; Kleemann, Wolfgang; Lu, Sheng-Guo

    2017-01-01

    Both relaxor ferroelectric and antiferroelectric materials can individually demonstrate large electrocaloric effects (ECE). However, in order to further enhance the ECE it is crucial to find a material system, which can exhibit simultaneously both relaxor ferroelectric and antiferroelectric properties, or easily convert from one into another in terms of the compositional tailoring. Here we report on a system, in which the structure can readily change from antiferroelectric into relaxor ferroelectric and vice versa. To this end relaxor ferroelectric Pb0.89La0.11(Zr0.7Ti0.3)0.9725O3 and antiferroelectric Pb0.93La0.07(Zr0.82Ti0.18)0.9825O3 ceramics were designed near the antiferroelectric-ferroelectric phase boundary line in the La2O3-PbZrO3-PbTiO3 phase diagram. Conventional solid state reaction processing was used to prepare the two compositions. The ECE properties were deduced from Maxwell relations and Landau-Ginzburg-Devonshire (LGD) phenomenological theory, respectively, and also directly controlled by a computer and measured by thermometry. Large electrocaloric efficiencies were obtained and comparable with the results calculated via the phenomenological theory. Results show great potential in achieving large cooling power as refrigerants. PMID:28345655

  14. Synthesis and physicochemical characterization of nanocrystalline cobalt doped lanthanum strontium ferrite

    NASA Astrophysics Data System (ADS)

    Nityanand, Chaubey; Nalin, Wani Bina; Rajkumar, Bharadwaj Shyamala; Chandra, Chattopadhyaya Mahesh

    2011-05-01

    Nanosized crystallites of La 0.6Sr 0.4Fe 0.8Co 0.2O 3- δ (LSCF), a promising cathode material for Intermediate Temperature-Solid Oxide Fuel Cells (IT-SOFCs) has been synthesized by alternative methods like ceramic route, polymerisable complex process and gel-combustion method and calcined at different temperatures. X-ray diffraction studies were used for the determination of phase purity, crystal structure and average crystallite size of the samples. Microstructure of LSCF samples was studied by SEM. Temperature-programmed reduction studies were done for evaluating the redox behavior of the samples prepared by alternative methods. The electrical conductivity measurements of sintered samples were carried out at elevated temperatures using four-probe method. The electrical conductivity of sample synthesized by gel-combustion method was more as compared to sample prepared by polymerisable complex process and ceramic route. The electrical conductivity decreased at high temperature due to loss of oxygen and the formation of oxygen vacancies. Thermo-dilatometry was used to study the linear thermal expansion behavior of the samples which shows that there is an observable increase in thermal expansion at high temperatures.

  15. The effect of LaBr3:Ce single crystal aliovalent co-doping on its mechanical strength

    NASA Astrophysics Data System (ADS)

    Benedetto, A.; Valladeau, S.; Richaud, D.; Ouspenski, V.; Gy, R.

    2015-06-01

    Lanthanum bromide cerium doped single crystals are a transparent scintillator material that offers outstanding scintillation properties with high light yield, excellent energy resolution, fast emission and excellent proportionality. Although properly packaged detectors are robust enough to withstand operating conditions during geophysical oil logging operations, the material itself is brittle and exhibits low fracture toughness. We attempted to modify the composition of the crystals through aliovalent co-doping by Ba, Ca, Hf, Sr, Zn and Zr. These elements have been added in concentrations from 100 ppm to 5000 ppm to the growth bath. Ratio of co-doping in the crystalline matrices ranged from no incorporation (for Hf, Zn, and Zr) up to 200 ppm for Sr and 10-20 ppm for Ca. The effect of the aliovalent co-doping on the mechanical properties of the crystals and in particular on their mechanical strength, hardness and toughness has been measured. As the crystals are extremely hygroscopic this demanded designing customized experiments in anhydrous environment in order to obtain reliable and accurate results. The ultimate strength has been measured by four points bending. Hardness has been measured by indentation and by the same technique we attempted to have some information on the fracture toughness. No improvement of the mechanical properties of the co-doped crystals with respect to the reference standard lanthanum bromide cerium doped could be found.

  16. Metamorphic modifications of the Muremera mafic-ultramafic intrusions, eastern Burundi, and their effect on chromite compositions

    NASA Astrophysics Data System (ADS)

    Evans, David M.

    2015-01-01

    The Muremera mafic-ultramafic intrusions were emplaced into metasedimentary rocks of the Karagwe-Ankole Belt in eastern Burundi, as part of the Mesoproterozoic Kibaran tectonomagmatic event. Igneous minerals of the Muremera intrusions have been partly altered to hydrous and carbonated metamorphic assemblages, although in most cases, the original igneous textures are well-preserved. Rounded, subhedral cumulus olivine has been partially and pseudomorphically replaced by lizardite-magnetite mesh-rim and lizardite-brucite mesh-centre assemblages, while anhedral interstitial plagioclase has been replaced by chlorite-tremolite. A later and localized event results in prograde alteration to antigorite-magnetite-chlorite-talc-carbonate and talc-carbonate-chlorite assemblages. The rocks are inferred to have undergone at least three separate metamorphic/alteration events resulting in: AS1 - an early alteration assemblage (mesh-rim lizardite-magnetite) characterized by very low fluid/rock ratios and widespread distribution; AS2 - a later, widespread low-temperature retrogressive (mesh-centre lizardite-brucite) assemblage associated with abundant close-spaced parallel veins; AS3 - later, prograde (antigorite-magnetite) and AT4 (talc-chlorite-carbonate) assemblages associated with more localized shearing and higher fluid/rock ratios. The AS1 assemblage most likely represents deuteric alteration that occurred soon after intrusion and cooling. The AS2 assemblage may relate to a continuation of this cooling, or may be correlated with the regional upright D2 folding event, while the AS3 and AT4 alteration assemblages are most likely correlated with the N-S oriented D3 faulting episode linked to the distal East African Orogeny. Euhedral to subhedral chromite grains are essentially unaltered where enclosed in primary unaltered olivine, pyroxene or plagioclase, as well as in AS1 lizardite-magnetite and AS2 lizardite-brucite altered olivine or pyroxene. In samples which show alteration

  17. Hearing Threshold, Loss, Noise Levels and Worker’s Profiles of an Open Cast Chromite Mines in Odisha, India

    PubMed Central

    Kerketta, Sunamani; Gartia, Rajendra; Bagh, Somanath

    2012-01-01

    Objectives: The aims of the study were to describe the noise levels at an open cast chromite mine in Odisha, India, and the hearing threshold of its workers and to associate their hearing loss with their age, work station and length of employment at the mine. Methods: We performed a cross-sectional study of the hearing threshold of chromite mine workers. Audiometric data from 500 subjects was collected at the mines’ hospital in the Sukinda Valley of Jajpur, Odisha, India. The latest audiometry data available for the period 2002 to 2008 was used in the analysis. Audiometric screening was performed using an audiometer (TRIVENI TAM-25 6025A) in a quiet environment by qualified technicians, audiologists or physicians. Tests were conducted on the subjects after they had completely rested for 16 hours or more after their day shift. Results: A maximum of 262 subjects (52.4%) were employed in the work zone area and a minimum of 2 subjects (0.4%) had less than 5 years working experience. The age of the subjects ranged from 29 to 59 years and their working experience ranged from 4 to 37 years. The subjects’ average mean hearing thresholds at 4, 6 and 8 kHz were 21.53 dBA, 23.40 dBA and 21.90 dBA, respectively. The maximum Leq and L90 levels exceeded the prescribed limits for commercial, residential and silence zones. The maximum Leq levels exceeded 95 dBA for large and medium heavy earth moving machineries (HEMMs), both outside and at the operator’s position. Hearing loss due to the subjects’ work experience was found to be greater than that attributable to age and workstation. Conclusion: In our study population, the maximum noise levels for large and medium HEMMs and inside the cabins of HEMMs were found to be more than 95 dBA. This indicates that operators in this particular chromite mine at Odisha, India were exposed to noise levels exceeding 95 dBA for more than 10% of the monitoring time. The subjects’ hearing loss was also found to increase for every 10-year

  18. Morphological effect of lanthanum-based supports on the catalytic performance of Pt catalysts in crotonaldehyde hydrogenation

    NASA Astrophysics Data System (ADS)

    Hou, Fengjun; Zhao, Huahua; Zhao, Jun; Yang, Jian; Yan, Liang; Song, Huangling; Chou, Lingjun

    2016-03-01

    Rod-like and particle-like La2O2CO3 and La2O3 were obtained via morphology-preserved thermal transformation of the La(OH)3 precursors. La2O2CO3- and La2O3-supported Pt catalysts were prepared by impregnation method and tested in the liquid-phase crotonaldehyde hydrogenation reaction. The textural and physicochemical properties of the samples were studied by a series of techniques including XRD, TG-DSC, N2 adsorption-desorption, TEM and HRTEM, IR spectrum, H2-TPD, and H2-TPR. Even after 600 °C reduction, Pt particles of about 0.8-2.8 nm interplayed with support surface to form Pt-doped interface, thereby preventing the catalysts from migration and affording a high dispersion of platinum. The specific exposed crystal-facets and surface oxygen species depending on the shape of the support affected the preferential deposition of Pt species and the metal-support interaction. Thus, Pt catalysts performed different physicochemical properties and catalytic performance relying on the morphology and structure of the supports. During the cycle experiment, severe deactivation was observed for NP-supported catalysts with an increased selectivity due to the aggregation and growth of Pt particles. Meantime, the NR-supported catalysts retained relatively high reactivity as a consequence of the crystal-facet confinement of rod-shaped lanthanum supports.

  19. In vitro bioequivalence approach for a locally acting gastrointestinal drug: lanthanum carbonate.

    PubMed

    Yang, Yongsheng; Shah, Rakhi B; Yu, Lawrence X; Khan, Mansoor A

    2013-02-04

    A conventional human pharmacokinetic (PK) in vivo study is often considered as the "gold standard" to determine bioequivalence (BE) of drug products. However, this BE approach is not always applicable to the products not intended to be delivered into the systemic circulation. For locally acting gastrointestinal (GI) products, well designed in vitro approaches might be more practical in that they are able not only to qualitatively predict the presence of the active substance at the site of action but also to specifically assess the performance of the active substance. For example, lanthanum carbonate chewable tablet, a locally acting GI phosphate binder when orally administrated, can release free lanthanum ions in the acid environment of the upper GI tract. The lanthanum ions directly reach the site of action to bind with dietary phosphate released from food to form highly insoluble lanthanum-phosphate complexes. This prevents the absorption of phosphate consequently reducing the serum phosphate. Thus, using a conventional PK approach to demonstrate BE is meaningless since plasma levels are not relevant for local efficacy in the GI tract. Additionally the bioavailability of lanthanum carbonate is less than 0.002%, and therefore, the PK approach is not feasible. Therefore, an alternative assessment method is required. This paper presents an in vitro approach that can be used in lieu of PK or clinical studies to determine the BE of lanthanum carbonate chewable tablets. It is hoped that this information can be used to finalize an in vitro guidance for BE studies of lanthanum carbonate chewable tablets as well as to assist with "in vivo" biowaiver decision making. The scientific information might be useful to the pharmaceutical industry for the purpose of planning and designing future BE studies.

  20. Conversion to lanthanum carbonate monotherapy effectively controls serum phosphorus with a reduced tablet burden: a multicenter open-label study

    PubMed Central

    2011-01-01

    Abstract Background Lanthanum carbonate (FOSRENOL®) is an effective, well-tolerated phosphate binder. The ability of lanthanum to reduce serum phosphorus levels to ≤5.5 mg/dL in patients with end-stage renal disease (ESRD) was assessed in a clinical practice setting. Methods A 16-week, phase IV study enrolled 2763 patients at 223 US sites to evaluate the efficacy of lanthanum carbonate in controlling serum phosphorus in patients with ESRD, and patient and physician satisfaction with, and preference for, lanthanum carbonate after conversion from other phosphate-binder medications. Patients received lanthanum carbonate prescriptions from physicians. These prescriptions were filled at local pharmacies rather than obtaining medication at the clinical trial site. Changes from serum phosphorus baseline values were analyzed using paired t tests. Patient and physician preferences for lanthanum carbonate versus previous medications were assessed using binomial proportion tests. Satisfaction was analyzed using the McNemar test. Daily dose, tablet burden, and laboratory values including albumin-adjusted serum calcium, calcium × phosphorus product, and parathyroid hormone levels were secondary endpoints. Results Serum phosphorus control (≤5.5 mg/dL) was effectively maintained in patients converting to lanthanum carbonate monotherapy; 41.6% of patients had controlled serum phosphate levels at 16 weeks. Patients and physicians expressed markedly higher satisfaction with lanthanum carbonate, and preferred lanthanum carbonate over previous medication. There were significant reductions in daily dose and daily tablet burden after conversion to lanthanum carbonate. Conclusions Serum phosphorus levels were effectively maintained in patients converted from other phosphate-binder medications to lanthanum carbonate, with increased satisfaction and reduced tablet burden. Trial Registration ClinicalTrials.gov: NCT0016012 PMID:21962172

  1. Process Developed for Generating Ceramic Interconnects With Low Sintering Temperatures for Solid Oxide Fuel Cells

    NASA Technical Reports Server (NTRS)

    Zhong, Zhi-Min; Goldsby, Jon C.

    2005-01-01

    Solid oxide fuel cells (SOFCs) have been considered as premium future power generation devices because they have demonstrated high energy-conversion efficiency, high power density, and extremely low pollution, and have the flexibility of using hydrocarbon fuel. The Solid-State Energy Conversion Alliance (SECA) initiative, supported by the U.S. Department of Energy and private industries, is leading the development and commercialization of SOFCs for low-cost stationary and automotive markets. The targeted power density for the initiative is rather low, so that the SECA SOFC can be operated at a relatively low temperature (approx. 700 C) and inexpensive metallic interconnects can be utilized in the SOFC stack. As only NASA can, the agency is investigating SOFCs for aerospace applications. Considerable high power density is required for the applications. As a result, the NASA SOFC will be operated at a high temperature (approx. 900 C) and ceramic interconnects will be employed. Lanthanum chromite-based materials have emerged as a leading candidate for the ceramic interconnects. The interconnects are expected to co-sinter with zirconia electrolyte to mitigate the interface electric resistance and to simplify the processing procedure. Lanthanum chromites made by the traditional method are sintered at 1500 C or above. They react with zirconia electrolytes (which typically sinter between 1300 and 1400 C) at the sintering temperature of lanthanum chromites. It has been envisioned that lanthanum chromites with lower sintering temperatures can be co-fired with zirconia electrolyte. Nonstoichiometric lanthanum chromites can be sintered at lower temperatures, but they are unstable and react with zirconia electrolyte during co-sintering. NASA Glenn Research Center s Ceramics Branch investigated a glycine nitrate process to generate fine powder of the lanthanum-chromite-based materials. By simultaneously doping calcium on the lanthanum site, and cobalt and aluminum on the

  2. Mean-field and density-functional studies of charge ordering and magnetic transitions in lanthanum manganites

    NASA Astrophysics Data System (ADS)

    Mishra, Snigdharaj Kumar

    Manganese oxides with perovskite structure exhibit many interesting properties. Recently colossal magnetoresistance (CMR) was observed in these oxides. They show extremely large change in electrical resistance in response to applied magnetic fields. This property has lots of technological relevance for the development of magnetic memory and switching devices. These oxides also show transitions from antiferromagnet to ferromagnet coupled with charge-order to charge-nonorder transition. In this dissertation we examine the electronic origin of these phenomena of lanthanum manganites by studying a model electronic Hamiltonian, which includes double-exchange, super-exchange, and Hubbard terms, using a combination of Hartree-Fock approximation and an exact diagonalization scheme. The existence of "canted" spin order is investigated at zero temperature. We find that the double-exchange mechanism does not always lead to a canted magnetic state, even for small carrier concentration. The canting may be suppressed in these compounds for the typical electronic parameters. We study the charge ordering and magnetic transitions in the perovskites by solving the Hamiltonian both at zero and finite temperature. At zero temperature as we increase the strength of the extended-Hubbard repulsion (Usb1), a first-order transition from a charge-non-ordered metallic ferromagnet (FN) to a charge-ordered, insulating antiferromagnet (AFO) is obtained. The AFO-FN transition is also obtained by increasing the temperature T. The melting of charge ordering as a function of temperature, doping concentration and magnetic field is also examined. Different phases are obtained as a function of temperature and doping concentration. These are in qualitative agreement with experimental data. We study the electronic structures of pyrochlores by the density-functional LMTO method and show that the double-exchange mechanism is relevant for these compounds as well.

  3. Titania-lanthanum phosphate photoactive and hydrophobic new generation catalyst

    SciTech Connect

    Jyothi, Chembolli K.; Jaimy, Kanakkanmavudi B.; Ghosh, Swapankumar; Sankar, Sasidharan; Smitha, V.S.; Warrier, K.G.K.

    2011-07-15

    Titania-lanthanum phosphate nanocomposites with multifunctional properties have been synthesized by aqueous sol-gel method. The precursor sols with varying TiO{sub 2}:LaPO{sub 4} ratios were applied as thin coating on glass substrates in order to be transparent, hydrophobic, photocatalytically active coatings. The phase compositions of the composite powders were identified by powder X-ray diffraction (XRD) and high-resolution transmission electron microscopy (HR-TEM). The anatase phase of TiO{sub 2} in TiO{sub 2}-LaPO{sub 4} composite precursors was found to be stable even on annealing at 800 deg. C. The glass substrates, coated with TL1 (TiO{sub 2}-LaPO{sub 4} composition with 1 mol% LaPO{sub 4}) and TL50 (composite precursor containing TiO{sub 2} and LaPO{sub 4} with molar ratio 1:1) sols and annealed at 400 deg. C, produced contact angles of 74 deg. and 92 deg., respectively, though it is only 62 deg. for pure TiO{sub 2} coating. The glass substrates, coated with TL50 sol, produced surfaces with relatively high roughness and uneven morphology. The TL1 material, annealed at 800 deg. C, has shown the highest UV photoactivity with an apparent rate constant, k{sub app}=24x10{sup -3} min{sup -1}, which is over five times higher than that observed with standard Hombikat UV 100 (k{sub app}=4x10{sup -3} min{sup -1}). The photoactivity combined with a moderate contact angle (85.3 deg.) shows that this material has a promise as an efficient self-cleaning precursor. - Graphical abstract: Multifunctional TiO{sub 2}-LaPO{sub 4} composite stabilizes anatase phase with enhanced photocatalytic activity, and moderately higher hydrophobicity is a promising material for self-cleaning application. Highlights: > Titania-lanthanum phosphate nanocomposites were synthesized by aqueous sol-gel method. > Transparent, hydrophobic, photoactive coatings were developed on glass substrates. > The glass substrates, coated with TL1 annealed at 400 deg. C, produced a contact angle of 74 deg

  4. Potentiometric measurement of polymer-membrane electrodes based on lanthanum

    SciTech Connect

    Saefurohman, Asep Buchari, Noviandri, Indra; Syoni

    2014-03-24

    Quantitative analysis of rare earth elements which are considered as the standard method that has a high accuracy, and detection limits achieved by the order of ppm is inductively coupled plasma atomic emission spectroscopy (ICPAES). But these tools are expensive and valuable analysis of the high cost of implementation. In this study be made and characterized selective electrode for the determination of rare earth ions is potentiometric. Membrane manufacturing techniques studied is based on immersion (liquid impregnated membrane) in PTFE 0.5 pore size. As ionophores to be used tri butyl phosphate (TBP) and bis(2-etylhexyl) hydrogen phosphate. There is no report previously that TBP used as ionophore in polymeric membrane based lanthanum. Some parameters that affect the performance of membrane electrode such as membrane composition, membrane thickness, and types of membrane materials studied in this research. Manufacturing of Ion Selective Electrodes (ISE) Lanthanum (La) by means of impregnation La membrane in TBP in kerosene solution has been done and showed performance for ISE-La. FTIR spectrum results for PTFE 0.5 pore size which impregnated in TBP and PTFE blank showed difference of spectra in the top 1257 cm{sup −1}, 1031 cm{sup −1} and 794.7 cm{sup −1} for P=O stretching and stretching POC from group −OP =O. The result showed shift wave number for P =O stretching of the cluster (−OP=O) in PTFE-TBP mixture that is at the peak of 1230 cm{sup −1} indicated that no interaction bond between hydroxyl group of molecules with molecular clusters fosforil of TBP or R{sub 3}P = O. The membrane had stable responses in pH range between 1 and 9. Good responses were obtained using 10{sup −3} M La(III) internal solution, which produced relatively high potential. ISE-La showed relatively good performances. The electrode had a response time of 29±4.5 second and could be use for 50 days. The linear range was between 10{sup −5} and 10{sup −1} M.

  5. Potentiometric measurement of polymer-membrane electrodes based on lanthanum

    NASA Astrophysics Data System (ADS)

    Saefurohman, Asep; Buchari, Noviandri, Indra; Syoni

    2014-03-01

    Quantitative analysis of rare earth elements which are considered as the standard method that has a high accuracy, and detection limits achieved by the order of ppm is inductively coupled plasma atomic emission spectroscopy (ICPAES). But these tools are expensive and valuable analysis of the high cost of implementation. In this study be made and characterized selective electrode for the determination of rare earth ions is potentiometric. Membrane manufacturing techniques studied is based on immersion (liquid impregnated membrane) in PTFE 0.5 pore size. As ionophores to be used tri butyl phosphate (TBP) and bis(2-etylhexyl) hydrogen phosphate. There is no report previously that TBP used as ionophore in polymeric membrane based lanthanum. Some parameters that affect the performance of membrane electrode such as membrane composition, membrane thickness, and types of membrane materials studied in this research. Manufacturing of Ion Selective Electrodes (ISE) Lanthanum (La) by means of impregnation La membrane in TBP in kerosene solution has been done and showed performance for ISE-La. FTIR spectrum results for PTFE 0.5 pore size which impregnated in TBP and PTFE blank showed difference of spectra in the top 1257 cm-1, 1031 cm-1 and 794.7 cm-1 for P=O stretching and stretching POC from group -OP =O. The result showed shift wave number for P =O stretching of the cluster (-OP=O) in PTFE-TBP mixture that is at the peak of 1230 cm-1 indicated that no interaction bond between hydroxyl group of molecules with molecular clusters fosforil of TBP or R3P = O. The membrane had stable responses in pH range between 1 and 9. Good responses were obtained using 10-3 M La(III) internal solution, which produced relatively high potential. ISE-La showed relatively good performances. The electrode had a response time of 29±4.5 second and could be use for 50 days. The linear range was between 10-5 and 10-1 M.

  6. Methanol synthesis using a catalyst combination of alkali or alkaline earth salts and reduced copper chromite for methanol synthesis

    DOEpatents

    Tierney, John W.; Wender, Irving; Palekar, Vishwesh M.

    1993-01-01

    The present invention relates to a novel route for the synthesis of methanol, and more specifically to the production of methanol by contacting synthesis gas under relatively mild conditions in a slurry phase with a catalyst combination comprising reduced copper chromite and basic alkali salts or alkaline earth salts. The present invention allows the synthesis of methanol to occur in the temperature range of approximately 100.degree.-160.degree. C. and the pressure range of 40-65 atm. The process produces methanol with up to 90% syngas conversion per pass and up to 95% methanol selectivity. The only major by-product is a small amount of easily separated methyl formate. Very small amounts of water, carbon dioxide and dimethyl ether are also produced. The present catalyst combination also is capable of tolerating fluctuations in the H.sub.2 /CO ratio without major deleterious effect on the reaction rate. Furthermore, carbon dioxide and water are also tolerated without substantial catalyst deactivation.

  7. Application of spinel-type cobalt chromite as a novel catalyst for combustion of chlorinated organic pollutants.

    PubMed

    Kim, D C; Ihm, S K

    2001-01-01

    Various chromium-containing catalysts were tested for the total oxidation of trichloroethylene (TCE) as a model reaction for the catalytic combustion of chlorinated organic pollutants. A spinel-type cobalt chromite (CoCr2O4) among others was proven to be a very promising catalyst showing higher activity and higher CO2 selectivity than traditional alumina supported chromia. Even if both Cr3+ and Cr6+ species were observed on the surface of CoCr2O4, the Cr6+ species was stable under reducing environment. The presence of Cr3+-Cr6+ pair sites and the effect of redox treatments on the activity were investigated to explain the nature of possible active sites for TCE decomposition. Higher selectivity to CO2 of CoCr2O4 was ascribed to the abundance of its Cr3+ species, together with its activity for water gas shift reaction.

  8. Complete zircon and chromite digestion by sintering of granite, rhyolite, andesite and harzburgite rock reference materials for geochronological purposes

    NASA Astrophysics Data System (ADS)

    Bokhari, Syed Nadeem H.; Meisel, Thomas

    2014-05-01

    Zircon (ZrSiO4) is a common accessory mineral in nature that occurs in a wide variety of sedimentary, igneous, and metamorphic rocks. Zircon has the ability to retain substantial chemical and isotopic information that are used in range of geochemical and geo- chronological investigations. Sample digestion of such rock types is a limiting factor due to the chemical inertness of zircon (ZrSiO4) tourmaline, chromite, barite, monazite, sphene, xenotime etc. as the accuracy of results relies mainly on recovery of analytes from these minerals. Dissolution by wet acid digestions are often incomplete and high blank and total dissolved solids (TDS) contents with alkali fusions lead to an underestimation of analyte concentrations. Hence an effective analytical procedure, that successfully dissolves refractory minerals such as zircon is needed to be employed for reliable analytical results. Na2O2 digestion [1] was applied in characterisation of granite (G-3), rhyolite (MRH), andesite (MGL-AND) and harzburgite (MUH-1) powdered reference material with solution based ICP-MS analysis. In this study we undertake a systematic evaluation of decomposition time and sample:Na2O2 ratio and test portion size after minimising effect of all other constraints that makes homogeneity ambiguous. In recovering zircon and chromite 100 mg test portion was mixed with different amounts of Na2O2 i.e. 100-600 mg. Impact of decomposition time was observed by systematically increasing heating time from 30-45 minutes to 90-120 minutes at 480°C. Different test portion sizes 100-500 mg of samples were digested to control variance of inhomogeneity. An improved recovery of zirconium in zircon in granite (G-3), rhyolite MRH), andesite (MGL-AND) and chromite in harzburgite (MUH-1) was obtained by increasing heating time (2h) at 480°C and by keeping (1:6) ratio of sample:Na2O2. Through this work it has been established that due to presence of zircon and chromite, decomposition time and sample:Na2O2 ratio has

  9. The implications of integrated assessment and modelling studies for the future remediation of chromite ore processing residue disposal sites.

    PubMed

    Farmer, J G; Paterson, E; Bewley, R J F; Geelhoed, J S; Hillier, S; Meeussen, J C L; Lumsdon, D G; Thomas, R P; Graham, M C

    2006-05-01

    Chromite ore processing residue (COPR) waste from a former chromium chemical works (1830-1968) is still contaminating groundwater in Glasgow, Scotland, with carcinogenic hexavalent chromium, Cr(VI). An integrated analytical, experimental and modelling approach has identified and accounted for mineral phases and processes responsible for the retention and release of Cr(VI) under prevailing field conditions. Both the nature of mineral phase retention and the buffered high pH of the sites, however, militate against direct remediative treatment of the source material, for example by the application of generic methods (e.g. FeSO4) that have been successfully employed elsewhere for the reduction of Cr(VI) to Cr(III) in other matrices. The interception and treatment of groundwater to remove Cr(VI) and the capping of sites to reduce human exposure to airborne Cr(VI)-contaminated dust may well be more realistic and effective, at least in the short to medium term.

  10. Application of potassium tetrafluorobromate to the rapid decomposition and determination of noble metals in chromites and related materials

    NASA Astrophysics Data System (ADS)

    Mitkin, V. N.; Zayakina, S. B.; Tsimbalist, V. G.; Galizky, A. A.

    2003-02-01

    Described is an effective new procedure for the preparation of chromites and other geological materials for the determination of the noble metals (NM). The procedure is based on the use of a mixture of KBrF 4 and KHF 2 obtained in situ by adding liquid BrF 3 to a mixture of KHF 2 and sample powder. South African Geostandards SARM-7 platinum ore from the Merensky Reef and SARM-65, a platinum-bearing chromite ore, were used for method development. Following fluorinative decomposition of samples, a homogeneous product is obtained which is suitable for instrumental analysis using either atomic absorption or emission spectrometry techniques. Sulfatization of fusion product using H 2SO 4 produces a non-hygroscopic material, which can be easily powdered and sampled directly into the argon plasma. Solution-based analytical techniques can be applied directly after fluorinative decomposition and conversion of resulting fluorides into chlorides by HCl treatment. The proposed new method, combined with spectrometric emission analysis of powders using a double-jet plasmatron dc plasma atomic emission spectrometry (AES) instrument achieved the following limits of detection (LOD) for the noble metals: Ag, Au and Pd: 1-2×10 -2 g/ton; Pt: 5×10 -2 g/ton; Ru, Rh, Ir and Os: 1-3×10 -3 g/ton. Graphic furnace atomic absorption spectrometry (GFAAS) with preliminary extraction, LODs for NMs were: Pt and Ru: 1×10 -2; Pd and Rh: 1×10 -3; Au and Ag: 1-2×10 -4 g/ton. The relative standard deviation of NM determinations was dependent on concentration and sample type but commonly was in the range of 3-15% dc plasma AES and 5-30% for extraction GFAAS.

  11. Chromites from the Gogoł;ów-Jordanów Serpentinite Massif (SW Poland) - evidence of the arc setting magmatism

    NASA Astrophysics Data System (ADS)

    Wojtulek, Piotr; Puziewicz, Jacek; Ntaflos, Theodoros; Bukała, Michał

    2014-05-01

    The Gogołów-Jordanów Serpentinite Massif (GJSM) is a peridotitic member of the Variscan Ślęża Ophiolite (SW Poland). Chromitite veinlets and pockets occur in the central part of the massif in the Czernica Hill area within completely serpentinized rocks. Chromitites consist of rounded chromite grains up to 4 cm and chlorite filling the interstices. The veins are embedded in serpentine-olivine-chlorite aggregates. Chemical composition of chromite occurring in chromitites defines two varieties. Chromite I (Cr# = 0.49 - 0.58) contains 23.32 - 28.36 wt.% Al2O3, 40.29 - 48.10 wt.% Cr2O3, 15.10 - 15.50 wt.% FeO, 14.50 - 15.50 wt.% MgO and ~0.1 wt.% TiO2. Chromite II (Cr# = 0.71 - 0.73) contains 13.83 - 15.24 wt.% Al2O3, 54.85 - 56.65 wt.% Cr2O3, 16.71 - 18.04 wt.% FeO, 10.62 - 11.59 wt.% MgO and 0.1 wt.% TiO2. Chromite grains are composed mostly of chromite I. Chromite II forms irregular spongy domains up to 150 µm, located at fissures or forming grain rims. The bulk chromitite composition of the massive ores reveals Rb, Ba, Pb and Sb enrichment relative to primitive mantle; Pt and Pd (up to 36 ppb) are also enriched relative to primitive mantle. Other phases coexisting with chromite are chlorite and olivine. Chlorite (Fe# = 0.02) contains 17.5 - 23.0 wt.% Al2O3, 0.6 - 1.8 wt.% Cr2O3 and 31.8 - 34.2 wt.% MgO. Olivine (Fo93.5-96.2) contains 0.44- 0.51 wt.% NiO. Olivine grains are zoned - the low-forsteritic cores are surrounded by high-forsteritic domain. Chromite II and chlorite are secondary phases and were probably formed due to greenschist facies metamorphism. Chromitites are cumuletes of melt blocked during its flow through peridotitic host. Low TiO2 content and moderate chromian number of the GJSM chromitites is typical for chromian spinels originated from melt derived from back arc depleted source (cf. Python et al., 2008, Gonzalez-Jimenez, 2011). The GJSM chromitites are rich in Al and poor in Pt and Pd what is typical for chromitites occurring in the

  12. Influence of lanthanum oxide as quality promoter on cathodes for MCFC

    NASA Astrophysics Data System (ADS)

    Escudero, M. J.; Nóvoa, X. R.; Rodrigo, T.; Daza, L.

    A novel material based on lithium nickel mixed oxides modified by lanthanum impregnation was investigated as an alternative cathode for molten carbonate fuel cells (MCFCs). The electrochemical behaviour of the new cathode material was evaluated in an eutectic mixture of lithium and potassium (Li:K, 62:38) at 650 °C by electrochemical impedance spectroscopy (EIS) as a function of lanthanum content, immersion time and gas composition. The impedance spectra inform on electrode structural changes during the first 100 h. The loss of lithium and the low dissolution of nickel and lanthanum are responsible of these changes. Later on, the structure reaches a stable state. The lanthanum-impregnated cathodes show higher catalytic activity for oxygen reduction and lower dissolution of nickel oxide than the lanthanum-free sample. The cathode material having 0.3 wt.% of La 2O 3 shows the best behaviour. The loss of lithium was confirmed by X-ray diffraction (XRD) and inductive coupled plasma-atomic emission spectroscopy (ICP-AES).

  13. Lanthanum carbonate stimulates bone formation in a rat model of renal insufficiency with low bone turnover.

    PubMed

    Fumoto, Toshio; Ito, Masako; Ikeda, Kyoji

    2014-09-01

    Control of phosphate is important in the management of chronic kidney disease with mineral and bone disorder (CKD-MBD), for which lanthanum carbonate, a non-calcium phosphate-binding agent, has recently been introduced; however, it remains to be determined whether it has any beneficial or deleterious effect on bone remodeling. In the present study, the effects of lanthanum carbonate were examined in an animal model that mimics low turnover bone disease in CKD, i.e., thyroparathyroidectomized (TPTX) and 5/6 nephrectomized (NX) rats undergoing a constant infusion of parathyroid hormone (PTH) and thyroxine injections (TPTX-PTH-5/6NX). Bone histomorphometry at the second lumbar vertebra and tibial metaphysis revealed that both bone formation and resorption were markedly suppressed in the TPTX-PTH-5/6NX model compared with the sham-operated control group, and treatment with lanthanum carbonate was associated with the stimulation of bone formation but not an acceleration of bone resorption. Lanthanum treatment caused a robust stimulation of bone formation with an activation of osteoblasts on the endosteal surface of femoral diaphysis, leading to an increase in cortical bone volume. Thus, lanthanum carbonate has the potential to stimulate bone formation in cases of CKD-MBD with suppressed bone turnover.

  14. Ordered mesoporous silica modified with lanthanum for ibuprofen loading and release behaviour.

    PubMed

    Goscianska, Joanna; Olejnik, Anna; Nowak, Izabela; Marciniak, Michal; Pietrzak, Robert

    2015-08-01

    The ordered mesoporous silicas SBA-15 and KIT-6, modified with lanthanum, have been for the first time applied in investigation of ibuprofen adsorption and release. The materials of hexagonal and regular structure were obtained by the hydrothermal method using a triblock copolymer Pluronic P123 as a template. The mesoporous silicas were impregnated with an aqueous solution of lanthanum(III) chloride in the amount necessary to obtain 1, 3 and 5wt.% La loading. The physicochemical properties of the modified silicas were characterised by X-ray diffraction, transmission electron microscopy, UV-Vis spectrophotometry and low-temperature nitrogen sorption. The results showed that lanthanum strongly determined structural as well as textural properties of the silicas. The samples of modified silica were checked for the ability to adsorb and release of ibuprofen. The storage capacity of the modified silicas obtained increased with increasing their average pore diameter and percentage content of lanthanum. The amount of ibuprofen adsorbed onto KIT-6 silica modified with La was higher than that adsorbed onto SBA-15 materials. The high coverage of lanthanum on the surface of KIT-6 and SBA-15 solids was found to increase the amount of ibuprofen and the rate of its release.

  15. Processing Techniques Developed to Fabricate Lanthanum Titanate Piezoceramic Material for High-Temperature Smart Structures

    NASA Technical Reports Server (NTRS)

    Goldsby, Jon C.; Farmer, Serene C.; Sayir, Ali

    2004-01-01

    Piezoelectric ceramic materials are potential candidates for use as actuators and sensors in intelligent gas turbine engines. For piezoceramics to be applied in gas turbine engines, they will have to be able to function in temperatures ranging from 1000 to 2500 F. However, the maximum use temperature for state-of-the-art piezoceramic materials is on the order of 300 to 400 F. Research activities have been initiated to develop high-temperature piezoceramic materials for gas turbine engine applications. Lanthanum titanate has been shown to have high-temperature piezoelectric properties with Curie temperatures of T(sub c) = 1500 C and use temperatures greater than 1000 C. However, the fabrication of lanthanum titanate poses serious challenges because of the very high sintering temperatures required for densification. Two different techniques have been developed at the NASA Glenn Research Center to fabricate dense lanthanum titanate piezoceramic material. In one approach, lower sintering temperatures were achieved by adding yttrium oxide to commercially available lanthanum titanate powder. Addition of only 0.1 mol% yttrium oxide lowered the sintering temperature by as much as 300 C, to just 1100 C, and dense lanthanum titanate was produced by pressure-assisted sintering. The second approach utilized the same commercially available powders but used an innovative sintering approach called differential sintering, which did not require any additive.

  16. Removing Phosphorus from Aqueous Solutions Using Lanthanum Modified Pine Needles

    PubMed Central

    Wang, Xianze; Liu, Zhongmou; Liu, Jiancong; Huo, Mingxin; Huo, Hongliang; Yang, Wu

    2015-01-01

    The renewable pine needles was used as an adsorbent to remove phosphorus from aqueous solutions. Using batch experiments, pine needles pretreated with alkali-isopropanol (AI) failed to effectively remove phosphorus, while pine needles modified with lanthanum hydroxide (LH) showed relatively high removal efficiency. LH pine needles were effective at a wide pH ranges, with the highest removal efficiency reaching approximately 85% at a pH of 3. The removal efficiency was kept above 65% using 10 mg/L phosphorus solutions at desired pH values. There was no apparent significant competitive behavior between co-existing anions of sulfate, nitrate, and chloride (SO42-, NO3- and Cl-); however, CO32- exhibited increased interfering behavior as concentrations increased. An intraparticle diffusion model showed that the adsorption process occurred in three phases, suggesting that a boundary layer adsorption phenomena slightly affected the adsorption process, and that intraparticle diffusion was dominant. The adsorption process was thermodynamically unfavorable and non-spontaneous; temperature increases improved phosphorus removal. Total organic carbon (TOC) assays indicated that chemical modification reduced the release of soluble organic compounds from 135.6 mg/L to 7.76 mg/L. This new information about adsorption performances provides valuable information, and can inform future technological applications designed to remove phosphorus from aqueous solutions. PMID:26630014

  17. Electronic Transitions and Spin-Orbit Splitting of Lanthanum Dimer

    NASA Astrophysics Data System (ADS)

    Liu, Yang; Wu, Lu; Zhang, Changhua; Yang, Dong-Sheng

    2011-06-01

    Lanthanum dimer (La_2) was studied by mass-analyzed threshold ionization (MATI) spectroscopy and a series of high-level multi-configuration ab initio calculations (CASSCF, CASPT2, and MRCI). The MATI spectrum exhibits three band systems originating at 39044, 40312, and 40862 Cm-1, respectively. Above the band origin, the first band system displays a vibrational progression of ˜232 Cm-1, and the other two show vibrational progression with the same interval of ˜240 Cm-1. Below the band origin, the three systems exhibit the same vibrational interval of ˜207 Cm-1. These band systems are assigned to three electronic transitions from the ground state of La_2 to the low-lying electronic states of La_2^+: ^2Σ^+_g ← ^1Σ^+_g, ^2Πu,1/2 ← ^1Σ^+_g, and ^2Πu,3/2 ← ^1Σ^+_g. The spin-orbit splitting in the ^2ΠU ion state is 550 Cm-1. In addition, the electronic states and bonding of La_2 will be compared with those of Sc_2 and Y_2.

  18. Lanthanum Titanate Nanoparticles ER Fluids with High Performance

    NASA Astrophysics Data System (ADS)

    Wang, De; Shen, Rong; Wei, Shiqiang; Lu, Kunquan

    A new type of electrorheological (ER) fluid consisting of lanthanum titanate (LTO) nanoparticles is developed. The ER fluids were prepared by suspending LTO powder in silicone oil and the particles were fabricated by wet chemical method. This ER fluid shows excellent ER properties: The static yield stress reaches over 150 kPa under 5 kV/mm with linear dependence on the applied DC electric field, and the current density is below 10 μA/cm2. In order to investigate the affect factor on the ER behavior, the LTO powder were heated under different temperatures. The ER performances of two particles treated under different temperatures were compared and the composition changes for those particles were analyzed with TG-FTIR technique. It was found that the static yield stress of the suspensions fell from over 150 kPa to about 40 kPa and the current densities decreased prominently as the rise of the heating temperature. TG-FTIR analysis indicated that polar groups remained in the particles such as alkyl group, hydroxyl group and carbonyl group etc., contribute to the ER effect significantly. The experimental results are helpful to understand the mechanism of the high ER effect and to synthesize better ER materials.

  19. Amorphous lithium lanthanum titanate for solid-state microbatteries

    DOE PAGES

    Lee, Jungwoo Z.; Wang, Ziying; Xin, Huolin L.; ...

    2016-12-16

    Lithium lanthanum titanate (LLTO) is a promising solid state electrolyte for solid state batteries due to its demonstrated high bulk ionic conductivity. However, crystalline LLTO has a relatively low grain boundary conductivity, limiting the overall material conductivity. In this work, we investigate amorphous LLTO (a-LLTO) thin films grown by pulsed laser deposition (PLD). By controlling the background pressure and temperature we are able to optimize the ionic conductivity to 3 × 10–4 S/cm and electronic conductivity to 5 × 10–11 S/cm. XRD, TEM, and STEM/EELS analysis confirm that the films are amorphous and indicate that oxygen background gas is necessarymore » during the PLD process to decrease the oxygen vacancy concentration, decreasing the electrical conductivity. Amorphous LLTO is deposited onto high voltage LiNi0.5Mn1.5O4 (LNMO) spinel cathode thin films and cycled up to 4.8 V vs. Li showing excellent capacity retention. Finally, these results demonstrate that a-LLTO has the potential to be integrated into high voltage thin film batteries.« less

  20. Amorphous lithium lanthanum titanate for solid-state microbatteries

    SciTech Connect

    Lee, Jungwoo Z.; Wang, Ziying; Xin, Huolin L.; Wynn, Thomas A.; Meng, Ying Shirley

    2016-12-16

    Lithium lanthanum titanate (LLTO) is a promising solid state electrolyte for solid state batteries due to its demonstrated high bulk ionic conductivity. However, crystalline LLTO has a relatively low grain boundary conductivity, limiting the overall material conductivity. In this work, we investigate amorphous LLTO (a-LLTO) thin films grown by pulsed laser deposition (PLD). By controlling the background pressure and temperature we are able to optimize the ionic conductivity to 3 × 10–4 S/cm and electronic conductivity to 5 × 10–11 S/cm. XRD, TEM, and STEM/EELS analysis confirm that the films are amorphous and indicate that oxygen background gas is necessary during the PLD process to decrease the oxygen vacancy concentration, decreasing the electrical conductivity. Amorphous LLTO is deposited onto high voltage LiNi0.5Mn1.5O4 (LNMO) spinel cathode thin films and cycled up to 4.8 V vs. Li showing excellent capacity retention. Finally, these results demonstrate that a-LLTO has the potential to be integrated into high voltage thin film batteries.

  1. The Bayo Canyon/radioactive lanthanum (RaLa) program

    SciTech Connect

    Dummer, J.E.; Taschner, J.C.; Courtright, C.C.

    1996-04-01

    LANL conducted 254 radioactive lanthanum (RaLa) implosion experiments Sept. 1944-March 1962, in order to test implosion designs for nuclear weapons. High explosives surrounding common metals (surrogates for Pu) and a radioactive source containing up to several thousand curies of La, were involved in each experiment. The resulting cloud was deposited as fallout, often to distances of several miles. This report was prepared to summarize existing records as an aid in evaluating the off-site impact, if any, of this 18-year program. The report provides a historical setting for the program, which was conducted in Technical Area 10, Bayo Canyon about 3 miles east of Los Alamos. A description of the site is followed by a discussion of collateral experiments conducted in 1950 by US Air Force for developing an airborne detector for tracking atmospheric nuclear weapons tests. All known off-site data from the RaLa program are tabulated and discussed. Besides the radiolanthanum, other potential trace radioactive material that may have been present in the fallout is discussed and amounts estimated. Off-site safety considerations are discussed; a preliminary off-site dose assessment is made. Bibliographical data on 33 persons important to the program are presented as footnotes.

  2. Chemical synthesis and supercapacitive properties of lanthanum telluride thin film.

    PubMed

    Patil, S J; Lokhande, A C; Lee, D-W; Kim, J H; Lokhande, C D

    2017-03-15

    Lanthanum telluride (La2Te3) thin films are synthesized via a successive ionic layer adsorption and reaction (SILAR) method. The crystal structure, surface morphology and surface wettability properties are investigated using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), Field emission scanning electron microscopy (FE-SEM) and contact angle goniometer techniques, respectively. The La2Te3 material exhibits a specific surface area of 51m(2)g(-1) determined by Brunauer-Emmett-Teller (BET) method. La2Te3 thin film electrode has a hydrophilic surface which consists of interconnected pine leaf-like flaky arrays that affect the performance of the supercapacitor. The supercapacitive performance of La2Te3 film electrode is evaluated in 1M LiClO4/PC electrolyte using cyclic voltammetry, galvanostatic charge-discharge, and electrochemical impedance spectroscopy techniques. La2Te3 film electrode exhibits a specific capacitance of 194Fg(-1) at a scan rate of 5mVs(-1) and stored energy density of 60Whkg(-1) with delivering power density of 7.22kWkg(-1). La2Te3 film electrode showed capacitive retention of 82% over 1000cycles at a scan rate of 100mVs(-1). Further, flexible La2Te3|LiClO4-PVA|La2Te3 supercapacitor cell is fabricated.

  3. Work function measurement of lanthanum-boron compounds

    NASA Technical Reports Server (NTRS)

    Jacobson, D. L.; Storms, E. K.

    1978-01-01

    The relationship between emission properties and sample composition is studied for lanthanum-boron compounds. Specifically, the La-B system is considered between 1400 and 2100 K and between LaB(4.24) and LaB(29.2) to determine the phase relationship, chemical activity of the compounds, vapor composition, and vaporization rate. The results indicate that: (1) a blue-colored phase near LaB(9) exists between a purple-colored LaB(6) and elemental boron, (2) vaporization is sufficiently more rapid than diffusion so that great compositional differences exist between the surface and the interior, (3) an activation energy lowers the boron vaporization rate from LaB(6), and (4) a steady-state surface composition between LaB(6.04) and LaB(6.07) exists for freely vaporizing materials as a function of interior composition, purity, and temperature. It is noted that the ultimate life of a thermionic diode is governed by electrode vaporization rate whereas efficiency is governed by the electrode work function.

  4. Investigation of lanthanum-strontium-cobalt ferrites using laser ablation inductively coupled plasma-mass spectrometry

    NASA Astrophysics Data System (ADS)

    Óvári, Mihály; Tarsoly, Gergely; Németh, Zoltán; Mihucz, Victor G.; Záray, Gyula

    2017-01-01

    In the present study, suitability of laser-ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) for characterization of the purity and homogeneity of lanthanum-strontium-cobalt ferrite (LSCF) ceramic microsamples with general formula La1 - xSrxFe0.025Co0.975O3 (0.00 ≤ x ≤ 0.50) was studied through determination of their Sr:La ratios as well as Sr content either in depth or line profiling mode. The Sr content of the LSCF samples expressed as weight percent ranged between 5.8% and 9.7% in the case of wet chemical ICP-MS analysis, while theoretical values varied from 5.5% to 9.4%. In the case of LA-ICP-MS, relative standard deviation of the La-normalized Sr intensities was sufficient to characterize the homogeneity of the studied samples. Major and trace element (Mn, Ni, Cu, Mg, Al, Ba) concentrations could be detected at medium resolution of the applied sector field ICP-MS instrument after microwave-assisted acid digestion. For depth and line profiling, a successful approach consisted of the normalization of intensities of Sr, Fe and Co with the corresponding La counts. For the determination of the elemental ratios of La and Sr, the methods involving LA were in good agreement with theoretical values by standardization to an in-house standard corresponding to the LSCF sample having the highest x value (i.e., 0.50) checked by wet chemical ICP-MS measurements. Thus, assessment of fine scale doping of synthesized perovskite type of microsamples could be achieved by the proposed LA-ICP-MS based on a novel calibration approach applying an in-house perovskite standard. Therefore, LA-ICP-MS can be recommended for quality control of perovskite-based products. In memoriam Attila Vértes (1934-2011), full professor of the Institute of Chemistry, Eötvös Loránd University, Budapest, Hungary.

  5. Fabrication of large-volume, low-cost ceramic lanthanum halide scintillators for gamma ray detection : final report for DHS/DNDO/TRDD project TA-01-SL01.

    SciTech Connect

    Boyle, Timothy J.; Ottley, Leigh Anna M.; Yang, Pin; Chen, Ching-Fong; Sanchez, Margaret R.; Bell, Nelson Simmons

    2008-10-01

    This project uses advanced ceramic processes to fabricate large, optical-quality, polycrystalline lanthanum halide scintillators to replace small single crystals produced by the conventional Bridgman growth method. The new approach not only removes the size constraint imposed by the growth method, but also offers the potential advantages of both reducing manufacturing cost and increasing production rate. The project goal is to fabricate dense lanthanum halide ceramics with a preferred crystal orientation by applying texture engineering and solid-state conversion to reduce the thermal mechanical stress in the ceramic and minimize scintillation light scattering at grain boundaries. Ultimately, this method could deliver the sought-after high sensitivity and <3% energy resolution at 662 keV of lanthanum halide scintillators and unleash their full potential for advanced gamma ray detection, enabling rapid identification of radioactive materials in a variety of practical applications. This report documents processing details from powder synthesis, seed particle growth, to final densification and texture development of cerium doped lanthanum bromide (LaBr{sub 3}:Ce{sup +3}) ceramics. This investigation demonstrated that: (1) A rapid, flexible, cost efficient synthesis method of anhydrous lanthanum halides and their solid solutions was developed. Several batches of ultrafine LaBr{sub 3}:Ce{sup +3} powder, free of oxyhalide, were produced by a rigorously controlled process. (2) Micron size ({approx} 5 {micro}m), platelet shape LaBr{sub 3} seed particles of high purity can be synthesized by a vapor phase transport process. (3) High aspect-ratio seed particles can be effectively aligned in the shear direction in the ceramic matrix, using a rotational shear-forming process. (4) Small size, highly translucent LaBr{sub 3} (0.25-inch diameter, 0.08-inch thick) samples were successfully fabricated by the equal channel angular consolidation process. (5) Large size, high density

  6. Fabrication of Nanosized Lanthanum Zirconate Powder and Deposition of Thermal Barrier Coating by Plasma Spray Process

    NASA Astrophysics Data System (ADS)

    Mishra, S. K.; Jagdeesh, N.; Pathak, L. C.

    2016-07-01

    The present manuscript discusses our findings on fabrication of nanosized lanthanum zirconate powder for thermal barrier coating application and its coating by plasma spray on nickel-based superalloy substrate. Single-phase La2Zr2O7 coating of thickness of the order of 45 µm on the Ni-Cr-Al bond coat coated Ni-based superalloy substrate was deposited by plasma spray process. The layers at the interface did not show spallation and inter diffusion was very less. The microstructure, interface, porosity, and mechanical properties of different layers are investigated. The lanthanum zirconate hardness and modulus were 10.5 and 277 GPa, respectively. The load depth curve for lanthanum zirconate showed good elastic recovery around 74%.

  7. [Efficacy and safety of lanthanum carbonate in chronic kidney disease patients with hyperphosphataemia].

    PubMed

    Laville, Maurice

    2011-06-01

    Hyperphosphataemia is a frequent complication in patients with chronic kidney disease and is associated with increased cardiovascular morbidity. Lanthanum carbonate is a calcium-free phosphate binder indicated in patients with chronic kidney disease. Its digestive absorption is minimal (<0,002%). This minimal quantity is rapidly excreted by the hepatobiliary system, but there is an initial accumulation in liver and bone, which reaches a plateau within a few weeks. Long-term follow-up until six years did not show any bone or liver toxicity. Efficacy and safety of lanthanum carbonate have been assessed in randomized trials. The most common side effects reported were gastrointestinal and occurred with a similar incidence than with placebo and other phosphate binders. Hypercalcemia was less frequent than with calcium carbonate. This review highlights pharmacokinetic, pharmacodynamic and clinical (efficacy and safety) properties of lanthanum carbonate and discusses its place in the management of hyperphosphataemia in patients with chronic kidney disease.

  8. Nanocomposite Lanthanum Zirconate Thermal Barrier Coating Deposited by Suspension Plasma Spray Process

    NASA Astrophysics Data System (ADS)

    Wang, Chaohui; Wang, You; Wang, Liang; Hao, Guangzhao; Sun, Xiaoguang; Shan, Fan; Zou, Zhiwei

    2014-10-01

    This work seeks to develop an innovative nanocomposite thermal barrier coating (TBC) exhibiting low thermal conductivity and high durability compared with that of current TBCs. To achieve this objective, nanosized lanthanum zirconate particles were selected for the topcoat of the TBC system, and a new process—suspension plasma spray—was employed to produce desirable microstructural features: the nanocomposite lanthanum zirconate TBC contains ultrafine splats and high volume porosity, for lower thermal conductivity, and better durability. The parameters of plasma spray experiment included two main variables: (i) spray distance varying from 40 to 80 mm and (ii) the concentration of suspension 20, 25, and 30 wt.%, respectively. The microstructure of obtained coatings was characterized with scanning electron microscope and x-ray diffraction. The porosity of coatings is in the range of 6-10%, and the single phase in the as-sprayed coatings was pyrochlore lanthanum zirconate.

  9. Eucalyptus tolerance mechanisms to lanthanum and cerium: subcellular distribution, antioxidant system and thiol pools.

    PubMed

    Shen, Yichang; Zhang, Shirong; Li, Sen; Xu, Xiaoxun; Jia, Yongxia; Gong, Guoshu

    2014-12-01

    Guanglin 9 (Eucalyptus grandis × Eucalyptus urophlla) and Eucalyptus grandis 5 are two eucalyptus species which have been found to grow normally in soils contaminated with lanthanum and cerium, but the tolerance mechanisms are not clear yet. In this study, a pot experiment was conducted to investigate the tolerance mechanisms of the eucalyptus to lanthanum and cerium. Cell walls stored 45.40-63.44% of the metals under lanthanum or cerium stress. Peroxidase and catalase activities enhanced with increasing soil La or Ce concentrations up to 200 mg kg(-1), while there were no obvious changes in glutathione and ascorbate concentrations. Non-protein thiols concentrations increased with increasing treatment levels up to 200 mg kg(-1), and then decreased. Phytochelatins concentrations continued to increase under La or Ce stress. Therefore, the two eucalyptus species are La and Ce tolerant plants, and the tolerance mechanisms include cell wall deposition, antioxidant system response, and thiol compound synthesis.

  10. Eutrophication management in surface waters using lanthanum modified bentonite: A review.

    PubMed

    Copetti, Diego; Finsterle, Karin; Marziali, Laura; Stefani, Fabrizio; Tartari, Gianni; Douglas, Grant; Reitzel, Kasper; Spears, Bryan M; Winfield, Ian J; Crosa, Giuseppe; D'Haese, Patrick; Yasseri, Said; Lürling, Miquel

    2016-06-15

    This paper reviews the scientific knowledge on the use of a lanthanum modified bentonite (LMB) to manage eutrophication in surface water. The LMB has been applied in around 200 environments worldwide and it has undergone extensive testing at laboratory, mesocosm, and whole lake scales. The available data underline a high efficiency for phosphorus binding. This efficiency can be limited by the presence of humic substances and competing oxyanions. Lanthanum concentrations detected during a LMB application are generally below acute toxicological threshold of different organisms, except in low alkalinity waters. To date there are no indications for long-term negative effects on LMB treated ecosystems, but issues related to La accumulation, increase of suspended solids and drastic resources depletion still need to be explored, in particular for sediment dwelling organisms. Application of LMB in saline waters need a careful risk evaluation due to potential lanthanum release.

  11. Distribution of intravascularly injected lanthanum ions in ganglia of the autonomic nervous system of the rat.

    PubMed

    DePace, D M

    1984-12-01

    Intravascular injection of lanthanum revealed that tight junctions of capillaries in sympathetic ganglia are impermeable to small ions and thus behave like capillaries of the blood-brain barrier. The failure of lanthanum to accumulate in the extracellular space suggests that fenestrated capillaries are not as ion-permeable as use of horseradish peroxidase (HRP) by some authors has indicated. A possible toxic action associated with high concentrations of HRP may be responsible for the high permeability of this substance. Testing with lanthanum demonstrated that sympathetic ganglia possess anatomic features that provide a hematic barrier. The blood-ganglion barrier resembles, but has not yet been demonstrated to be as absolute as the blood-brain barrier.

  12. Lanthanum nitrate genotoxicity evaluation: Ames test, mouse micronucleus assay, and chromosome aberration test.

    PubMed

    Yang, Hui; Zhang, Xiaopeng; Liu, Haibo; Cui, Wenming; Zhang, Qiannan; Li, Yongning; Yu, Zhou; Jia, Xudong

    2016-11-01

    The increasing use of rare-earth elements (REE) and their compounds has led to their accumulation in the environment and has raised concern about their safety. The toxic effects of REE such as lanthanum are largely unknown; genotoxicity studies have been limited and results are controversial. We evaluated the genotoxicity of lanthanum nitrate (La(NO3)3) in several in vitro and in vivo tests, including bacterial reverse mutation assay (Ames test), mouse bone marrow micronucleus assay, and chromosome aberration assay. La(NO3)3 was not mutagenic in the Ames test. La(NO3)3 did not increase the frequencies of bone marrow micronuclei or chromosome aberration in the mouse after repeated treatments at oral doses up to 735 (females) and 855mg/kg (males). The compound did not increase the frequency of chromosome aberrations in CHO cells in vitro. These results indicate that lanthanum is not a genotoxic hazard.

  13. The role of chemical interactions between thorium, cerium, and lanthanum in lymphocyte toxicity.

    PubMed

    Oliveira, Monica S; Duarte, Isabelle M; Paiva, Amanda V; Yunes, Samira N; Almeida, Carlos E; Mattos, Rita C; Sarcinelli, Paula N

    2014-01-01

    Thorium, cerium, and lanthanum are metals present in several types of minerals, the most common of which is monazite. Cerium and lanthanum are elements in the lanthanides series. Thorium, an actinide metal, is a hazardous element due to its radioactive characteristics. There is a lack of information describing the possible chemical interactions among these elements and the effects they may have on humans. Toxicological analyses were performed using cell viability, cell death, and DNA damage assays. Chemical interactions were evaluated based on the Loewe additivity model. The results indicate that thorium and cerium individually have no toxic effects on lymphocytes. However, thorium associated with lanthanum increases the toxicity of this element, thereby reducing the viability of lymphocytes at low concentrations of metals in the mixture.

  14. Preparation of yttrium, lanthanum, cerium, and neodymium basic carbonate particles by homogeneous precipitation

    SciTech Connect

    Akinc, M.; Sordelet, D. )

    1987-07-01

    Uniform yttrium, lanthanum, cerium, and neodymium basic carbonate particles were prepared by homogeneous precipitation. Powders were characterized with respect to size, shape, crystal structure, and thermal decomposition behavior. Yttria precursor particles were spherical, monosized (0.4 {mu}m), and amorphous; whereas lanthana, neodymia, and ceria precursors were prismatic (ranging from 1 to 6 {mu}m in size) and crystalline. Crystal structure was found to be ancylite-type orthorhombic symmetry in all three cases. Upon heating in air, yttrium, lanthanum, and neodymium precursors underwent two-step decomposition to first form oxycarbonate and then oxide. Cerium hydroxycarbonate decomposed in a single step to form the oxide.

  15. High-efficiency, low-temperature cesium diodes with lanthanum-hexaboride electrodes

    NASA Technical Reports Server (NTRS)

    Morris, J. F.

    1974-01-01

    Lanthanum hexaboride electrodes in 1700 K cesium diodes may triple power outputs compared with those demonstrated for nuclear thermionic space applications. Still greater relative gains seem possible for emitters below 1700 K. Further improvements in cesium diode performance should result from the lower collector temperatures allowed for earth and low power space duties. Decreased temperatures will lessen thermal transport losses that attend thermionic conversion mechanisms. Such advantages will add to those from collector Carnot and electrode effects. If plasma ignition difficulties impede diode temperature reductions, recycling small fractions of the output power could provide ionization. So high efficiency, low temperature cesium diodes with lanthanum hexaboride electrodes appear feasible.

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

    SciTech Connect

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

    1982-01-01

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

  17. Study of prolonged administration of lanthanum carbonate in dialysis patients.

    PubMed

    Gotoh, Junichi; Kukita, Kazutaka; Tsuchihashi, Seiichiro; Hattori, Masahiro; Iida, Junichi; Horie, Takashi; Onodera, Kazuhiko; Furui, Hidenori; Tamaki, Toru; Meguro, Junichi; Yonekawa, Motoki; Kawamura, Akio

    2013-04-01

    Data of 36 months were accumulated regarding the effects of lanthanum carbonate (LA) on serum phosphate concentrations in dialysis patients. Fifty-three patients (average age and dialysis history 58.4 years and 9.1 years) were included in this study who have been receiving outpatient treatment since March 2009, and who have been unable to maintain serum phosphate concentrations of ≤6.0 mg/dL via traditional therapeutic agents used for hyperphosphatemia. Patients were given dosage of LA in addition to, or instead of, co-hyperphosphatemia treatments already being received. Mean dosages of calcium carbonate (CC) and sevelamer hydrochloride (SH) before starting LA administration were 1301.9 mg and 2462.3 mg, respectively. Dosage of LA for all cases was 750 mg at initial dose; 1528.3 mg at 5 months; and 1416.7 mg at 30 months. Dosage of other phosphate binders were 905.7 mg of CC and 820.8 mg of SH at 5 months; and 687.5 mg of CC and 1031.3 mg of SH at 30 months. Serum phosphorus levels (P levels) were significantly decreased at 1 month of LA administration, and continued until 30 months of La treatment. These results suggest that LA successfully controlled serum P and Ca concentrations simultaneously within target ranges without affecting serum intact parathyroid hormone concentration, although further long-term prospective cohort study on LA would be required.

  18. Microwave absorption in single crystals of lanthanum aluminate

    NASA Astrophysics Data System (ADS)

    Zuccaro, Claudio; Winter, Michael; Klein, Norbert; Urban, Knut

    1997-12-01

    A very sensitive dielectric resonator technique is employed to measure loss tangent tan δ and relative permittivity ɛr of lanthanum aluminate (LaAlO3) single crystals at 4-300 K and 4-12 GHz. A variety of single crystals grown by different techniques and purchased from different suppliers are considered. For T>150 K the loss tangent tan δ is almost sample independent with linear frequency dependence and monotonous temperature variation from 8×10-6 at 300 K to 2.5×10-6 at 150 K and 4.1 GHz. In this temperature range the experimental data are explained by a model based on lifetime broadened two-phonon difference processes. The loss tangent below 150 K is characterized by a peak in tan δ(T) at about 70 K. The height of this peak is frequency and strongly sample dependent. This leads to a variation of the loss tangent from 10-6 to 1.5×10-5 at 77 K and 8.6 GHz, the lowest values are generally achieved with Verneuil grown crystals and approach the intrinsic lower limit predicted by the phonon model. The peak is explained by defect dipole relaxation (local motions of ions). The activation energy of the relaxation process is determined from the measured data to be 31 meV. This low value indicates that the defect dipoles are associated with interstitials, possibly impurities in interstitial positions. Considering absorption due to phonons and due to defect dipole relaxation the loss tangent is calculated for a wide frequency range.

  19. Enantioselective DNA condensation induced by heptameric lanthanum helical supramolecular enantiomers.

    PubMed

    Bao, Fei-Fei; Xu, Xin-Xin; Zhou, Wen; Pang, Chun-Yan; Li, Zaijun; Gu, Zhi-Guo

    2014-09-01

    DNA condensation induced by a pair of heptameric La(III) helical enantiomers M-[La7(S-L)6(CO3)(NO3)6(OCH3)(CH3OH)7]·2CH3OH·5H2O and P-[La7(R-L)6(CO3)(NO3)6(OCH3)(CH3OH)5(H2O)2]·2CH3OH·4H2O (M-La and P-La, L=2-(2-hydroxybenzylamino)-3-carbamoylpropanoic acid) has been investigated by UV/vis spectroscopy, fluorescence spectroscopy, CD spectroscopy, EMSA, RALS, DLS, and SEM. The enantiomers M-La and P-La could induce CT-DNA condensation at a low concentration as observed in UV/vis spectroscopy. DNA condensates possessed globular nanoparticles with nearly homogeneous sizes in solid state determined by SEM (ca. 250 nm for M-La and ca. 200 nm for P-La). The enantiomers bound to DNA through electrostatic attraction and hydrogen bond interactions in a major groove, and rapidly condensed free DNA into its compact state. DNA decompaction has been acquired by using EDTA as disassembly agent, and analyzed by UV/vis spectroscopy, CD spectroscopy and EMSA. Moreover, the enantiomers M-La and P-La displayed discernible discrimination in DNA interaction and DNA condensation, as well as DNA decondensation. Our study suggested that lanthanum(III) enantiomers M-La and P-La were efficient DNA packaging agents with potential applications in gene delivery.

  20. Sorption of noble gases by solids, with reference to meteorites. II - Chromite and carbon. III - Sulfides, spinels, and other substances; on the origin of planetary gases

    NASA Technical Reports Server (NTRS)

    Yang, J.; Anders, E.

    1982-01-01

    The trapping of noble gases by chromite and carbon, two putative carriers of primordial noble gases in meteorites, was studied by synthesizing 19 samples in a Ne-Ar-Kr-Xe atmosphere at 440-720 K. Noble gas contents are found to approximately obey Henry's Law, but only slight correlations are found with composition, surface area, or adsorption temperature. Geometric mean distribution coefficients for bulk samples and HCl residues in 10 cu cm STP/g atm are: Xe 100, Kr 15, Ar 3.5, and Ne 0.62. Elemental fractionation data support the suggestion of Lewis et al. (1977) that chromite and carbon in C2 and C3 chondrites were formed by the reaction: Fe, Cr + 4CO yields (Fe, Cr)3O4 + 4C + carbides. In contrast to meteoritic minerals, the synthetic specimens show no isotopic fractionation of noble gases. In a subsequent study, attention is given to the cases of sulfides and spinels, on the way to consideration of the origin of planetary gases. Sulfides showed three distinctive trends relative to chromite or magnetite. The elemental fractionation pattern of Ar, Kr and Xe in meteorites, terrestrial rocks and planets resembles the adsorption patterns on the carbons, spinels, sulfides, and other solids studied. The high release temperature of meteoritic noble gases may be explained by transformation of the physisorbed or chemisorbed gas. The ready loss of meteoritic heavy gases on surficial oxidation is consistent with adsorption, as is the high abundance.

  1. PROCESS USING POTASSIUM LANTHANUM SULFATE FOR FORMING A CARRIER PRECIPITATE FOR PLUTONIUM VALUES

    DOEpatents

    Angerman, A.A.

    1958-10-21

    A process is presented for recovering plutonium values in an oxidation state not greater than +4 from fluoride-soluble fission products. The process consists of adding to an aqueous acidic solution of such plutonium values a crystalline potassium lanthanum sulfate precipitate which carries the plutonium values from the solution.

  2. Nickel/magnesium-lanthanum mixed oxide catalyst in the Kumada-coupling.

    PubMed

    Kiss, Arpád; Hell, Zoltán; Bálint, Mária

    2010-01-21

    A new, heterogeneous, magnesium-lanthanum mixed oxide solid base-supported nickel(ii) catalyst was developed. The catalyst was used successfully in the Kumada coupling of aryl halides, especially aryl bromides. The optimal reaction conditions of the coupling were determined.

  3. Comparative evaluation of the in vitro efficacy of lanthanum carbonate chewable tablets.

    PubMed

    Yang, Yongsheng; Bykadi, Srikant; Carlin, Alan S; Shah, Rakhi B; Yu, Lawrence X; Khan, Mansoor A

    2013-04-01

    The aims of this study were to systematically evaluate the effects of pH levels, phosphate concentrations, and tablet integrity on the phosphate binding profiles of lanthanum carbonate chewable tablets, and to compare the in vitro phosphate binding efficacy of one reference and two test products of lanthanum carbonate chewable tablets. Langmuir equation was utilized to calculate the binding constants k1 and k2 . The phosphate binding to the tablets of lanthanum carbonate product was pH dependent, with a faster binding rate at low pH. The crushed tablets bind phosphate more rapid. Compared with the whole tablets, the kinetic binding profiles from the crushed tablets were less variable under all conditions for both test and reference products. The phosphate level has a significant impact on the phosphate binding for both whole and crushed tablets under all pH conditions, with more binding at higher phosphate concentration. The phosphate binding profiles displayed significant difference among the products. For a crushed tablet, the phosphate binding to lanthanum reached equilibrium within 8 h under all conditions. The 90% confidence interval for the k2 ratio (test/reference) was well within the 80%-125% under all pH conditions. However, the k1 ratio varies from 54% to 144%. © 2013 Wiley Periodicals, Inc. and the American Pharmacists Association J Pharm Sci 102:1370-1381, 2013.

  4. Crystal growth and characterization of LaMAl 11O 19 lanthanum aluminates

    NASA Astrophysics Data System (ADS)

    Laville, F.; Lejus, A. M.

    1983-10-01

    New magnetoplumbite-type lanthanum aluminates with the formula LaMAl 11O 19 (M 2+ = Ni 2+, Co 2+, Fe 2+, Mg 1- xMn x, 0≤ x ≤1, have been grown as large single crystals using the Verneuil process or the floating zone method. Some characteristics of these crystals are given.

  5. Lanthanum chloride bidirectionally influences calcification in bovine vascular smooth muscle cells.

    PubMed

    Zhao, Wen-Hua; Gou, Bao-Di; Zhang, Tian-Lan; Wang, Kui

    2012-05-01

    Vascular calcification (VC) is frequent prevalence in patients with chronic kidney disease (CKD) and atherosclerosis. Lanthanum carbonate is used as an orally administered phosphate-binding agent to reduce the gastrointestinal absorption of phosphate and ameliorate VC in advanced CKD. In this study, we used bovine vascular smooth muscle cells as a model VC in vitro and studied the effects of lanthanum chloride on calcium deposition. Exposure of cells to LaCl(3) at the concentration of 0.1 µM suppressed the β-glycerophosphate-induced alkaline phosphatase activity and calcium deposition. Furthermore, LaCl(3) upregulated the β-glycerophosphate-suppressed expression of calcium-sensing receptor. In contrast to the inhibitory effect of LaCl(3) on calcium deposition, higher level lanthanum (50 µM) was found to promote immediately precipitation of calcium phosphate in cell culture medium. At this concentration, LaCl(3) was found to induce cell apoptosis which involves caspases-9 and -3. These data indicate that the promotory effect of LaCl(3) on calcium deposition is likely mediated by induction of apoptosis. Our in vitro findings do suggest that, in the context of raised lanthanum, greater attention should be paid to potential toxic effects associated to the use of lanthanide-based drugs.

  6. Spacecraft charging control by thermal, field emission with lanthanum-hexaboride emitters

    NASA Technical Reports Server (NTRS)

    Morris, J. F.

    1978-01-01

    Thermal, field emitters of lanthanum (or perhaps cerium) hexaboride (LaB6) with temperature variability up to about 1500K are suggested for spacecraft charging control. Such emitters operate at much lower voltages with considerably more control and add plasma-diagnostic versatility. These gains should outweigh the additional complexity of providing heat for the LaB6 thermal, field emitter.

  7. Fluoride removal in water by a hybrid adsorbent lanthanum-carbon.

    PubMed

    Vences-Alvarez, Esmeralda; Velazquez-Jimenez, Litza Halla; Chazaro-Ruiz, Luis Felipe; Diaz-Flores, Paola E; Rangel-Mendez, Jose Rene

    2015-10-01

    Various health problems associated with drinking water containing high fluoride levels, have motivated researchers to develop more efficient adsorbents to remove fluoride from water for beneficial concentrations to human health. The objective of this research was to anchor lanthanum oxyhydroxides on a commercial granular activated carbon (GAC) to remove fluoride from water considering the effect of the solution pH, and the presence of co-existing anions and organic matter. The activated carbon was modified with lanthanum oxyhydroxides by impregnation. SEM and XRD were performed in order to determine the crystal structure and morphology of the La(III) particles anchored on the GAC surface. FT-IR and pK(a)'s distribution were determined in order to elucidate both the possible mechanism of the lanthanum anchorage on the activated carbon surface and the fluoride adsorption mechanism on the modified material. The results showed that lanthanum ions prefer binding to carboxyl and phenolic groups on the activated carbon surface. Potentiometric titrations revealed that the modified carbon (GAC-La) possesses positive charge at a pH lower than 9. The adsorption capacity of the modified GAC increased five times in contrast to an unmodified GAC adsorption capacity at an initial F(-) concentration of 20 mg L(-1). Moreover, the presence of co-existing anions had no effect on the fluoride adsorption capacity at concentrations below 30 mg L(-1), that indicated high F(-) affinity by the modified adsorbent material (GAG-La).

  8. REFOS study: efficacy and safety of lanthanum carbonate in clinical practice in Spain.

    PubMed

    Torregrosa, José-Vicente; González-Parra, Emilio; González, M Teresa; Cannata-Andía, Jorge

    2014-05-21

    Lanthanum carbonate is a powerful phosphate binder that has shown efficacy and safety in clinical trials for hyperphosphataemia management, although there are few data in regular clinical practice. The study's objective was to evaluate, in regular clinical practice, its efficacy and safety in patients on dialysis. We retrospectively collected data from 15 months of monitoring, corresponding to 3 months prior to the start of treatment with lanthanum carbonate until 12 months after the start. Results included values of serum calcium, phosphorus, alkaline phosphatase, iPTH, hepatic enzymes and haemogram, as well as the daily-prescribed dose of lanthanum carbonate, the concomitant medication, treatment compliance and adverse events. 647 patients were included of which 522 completed the study. Abandonment, for the most part, was due to gastrointestinal disorders (26%) and hypophosphatemia (19%). Serum phosphorus decreased from 6.4±1.7 mg/dl (start) to 4.9±1.4 mg/dl (12 months) (P<.001). At the end of the monitoring period, 47% were within the desired phosphorus range (3.5-5mg/dl). There were no significant variations in the remaining parameters. Initial dose of lanthanum carbonate: 1900 mg/day; and end dose: 2300 mg/day. The variables independently associated with phosphataemia were baseline serum phosphorus and treatment compliance. In relation to safety, we observed 238 slight or moderate adverse effects in 117 patients, with 88% linked to gastrointestinal abnormalities. In conclusion, lanthanum carbonate reduces the serum phosphorus values in patients on dialysis with a good safety profile and acceptable adherence to that profile, with gastrointestinal disorders being the most frequent adverse effect.

  9. Gastrointestinal symptoms after the substitution of sevelamer hydrochloride with lanthanum carbonate in Japanese patients undergoing hemodialysis.

    PubMed

    Suzuki, D; Ichie, T; Hayashi, H; Sugiura, Y; Sugiyama, T

    2015-08-01

    Lanthanum carbonate has the same phosphorus depressant effect as the other phosphorus adsorbents, and is expected to decrease digestive symptom onset such as constipation in Japanese patients undergoing hemodialysis compared to sevelamar hydrochloride. In this study, we investigated the short- and long-term changes in digestive symptoms in these patients after substituting sevelamar hydrochloride with lanthanum carbonate. We studied 16 patients (4 men, 12 women) and evaluated their gastrointestinal symptoms before administration, at the time of administration, and 2, 4, 8, and 12 weeks after administration, using the Gastrointestinal Symptom Rating Scale. In addition, we conducted repeat evaluations 52 weeks after administration for the patients in whom lanthanum carbonate was administered continuously for 52 weeks. Fourteen (87.5%) out of the 16 patients could tolerate continuous administration for 12 weeks. The constipation score was 3.21 ± 1.74 before administration, 2.07 ± 0.83 2 weeks after administration, 1.76 ± 0.83 4 weeks after administration, 1.57 ± 0.56 8 weeks after administration, and 11.41 ± 0.48 12 weeks after administration. The scores improved significantly 4 weeks after administration (p < 0.05) and even 12 weeks after continuous administration. Among the 16 study patients, 9 patients (1 men, 8 women) were received lanthanum carbonate continuously for 52 weeks. The constipation score was 3.74 ± 1.92 at the start of administration, 1.37 ± 0.56 12 weeks after administration, and 1.85 ± 0.63 52 weeks after administration, with significant improvement even 52 weeks after administration (p < 0.05). This study shows that substituting sevelamar hydrochloride with lanthanum carbonate improves constipation symptoms in hemodialysis patients from an early stage, which indicates its usefulness in improving constipation symptoms caused by sevelamar hydrochloride.

  10. Lanthanum acetate inhibits vascular calcification induced by vitamin D3 plus nicotine in rats.

    PubMed

    Zhou, Ye-Bo; Jin, Shao-Ju; Cai, Yan; Teng, Xu; Chen, Li; Tang, Chao-Shu; Qi, Yong-Fen

    2009-08-01

    Lanthanum, a rare earth element, has been used to decrease serum phosphorus level in patients with chronic renal disease and hyperphosphatemia. We aimed to observe the effect and mechanism of two doses of lanthanum acetate (375 and 750 mg/kg/day) on vascular calcification induced by vitamin D3 plus nicotine treatment in rats for 4 weeks. As compared with control rats, rats with calcification showed widespread calcified nodules and irregular elastic fibers in calcified aorta on von Kossa calcium staining and increased aortic calcium and phosphorus contents, alkaline phosphatase (ALP) activity and bone-related protein expressions for osteopontin (OPN) and type III sodium dependent phosphate cotransporter Pit-1 (Pit-1). After treatment with either dose of lanthanum acetate, the calcified nodules and degree of irregular elastic fibers decreased in aortas. Lanthanum acetate at 750 mg/kg/day was more effective than 375 mg/kg/day in lessening vascular calcification by significantly reducing plasma phosphorus level, calcium x phosphorus product and ALP activity, by 30.3%, 28.6%, and 68.6%, respectively; reducing aortic phosphorus and calcium contents and ALP activity, by 48%, 53.1%, and 63.5% (all P < 0.01), respectively; reducing aortic mRNA level of OPN and Pit-1, by 55.8% (P < 0.01) and 38.8% (P < 0.05) and protein level of OPN and Pit-1, by 37.2% and 27.2% (both P < 0.01), respectively; and increasing carboxylated matrix Gla-protein (MGP) protein expression by 33.7% (P < 0.05), as compared with rats treated with vitamin D3 and nicotine alone. Lanthanum acetate could effectively inhibit the pathogenesis of vascular calcification.

  11. Identification of lanthanum-specific peptides for future recycling of rare earth elements from compact fluorescent lamps.

    PubMed

    Lederer, Franziska L; Curtis, Susan B; Bachmann, Stefanie; Dunbar, W Scott; MacGillivray, Ross T A

    2017-05-01

    As components of electronic scrap, rare earth minerals are an interesting but little used source of raw materials that are highly important for the recycling industry. Currently, there exists no cost-efficient technology to separate rare earth minerals from an electronic scrap mixture. In this study, phage surface display has been used as a key method to develop peptides with high specificity for particular inorganic targets in electronic scrap. Lanthanum phosphate doped with cerium and terbium as part of the fluorescent phosphors of spent compact fluorescent lamps (CFL) was used as a target material of economic interest to test the suitability of the phage display method to the separation of rare earth minerals. One random pVIII phage library was screened for peptide sequences that bind specifically to the fluorescent phosphor LaPO4 :Ce(3+) ,Tb(3+) (LAP). The library contained at least 100 binding pVIII peptides per phage particle with a diversity of 1 × 10(9) different phage per library. After three rounds of enrichment, a phage clone containing the surface peptide loop RCQYPLCS was found to bind specifically to LAP. Specificity and affinity of the identified phage bound peptide was confirmed by using binding and competition assays, immunofluorescence assays, and zeta potential measurements. Binding and immunofluorescence assays identified the peptide's affinity for the fluorescent phosphor components CAT (CeMgAl11 O19 :Tb(3+) ) and BAM (BaMgAl10 O17 :Eu(2+) ). No affinity was found for other fluorescent phosphor components such as YOX (Y2 O3 :Eu(3+) ). The binding specificity of the RCQYPLCS peptide loop was improved 3-51-fold by using alanine scanning mutagenesis. The identification of peptides with high specificity and affinity for special components in the fluorescent phosphor in CFLs provides a potentially new strategic approach to rare earth recycling. Biotechnol. Bioeng. 2017;114: 1016-1024. © 2016 Wiley Periodicals, Inc.

  12. Analysis of physico-chemical characteristics and metals in water sources of chromite mining in Sukinda Valley, Odisha, India.

    PubMed

    Dutta, Koushik; Ghosh, Apurba Ratan

    2013-07-01

    The extraction of chromite is being carried out since 1950 in Sukinda valley region of Odisha in India. Different physico-chemical parameters and level of metals in groundwater (tube well and dug well), surface water (Damsal nala), mining drainage water and bottom sediment of Damsal nala were analysed. The results revealed that the total Cr content of groundwater (0.04-0.07 ppm), Damsal nala (0.10 - 0.20 ppm) and mine drainage water (20.12-56.51 ppm) exceeded the permissible limit in all seasons. The Cr (VI) content of mine drainage water exceeded the permissible limit (0.05 ppm as per the recommendation of WHO). The pH (6.5-7.9), available N (6.27-18.82 kg ha(-1)), available PO4(-3) (15.39-123.11 kg ha(-1)), available K+ (21.07-410.89 kg ha(-1)) and organic matter (0.20-1.55%) content of bottom sediment of Damsal nala varied seasonally and the lowest values were found during monsoon. The physico-chemical characteristics of water from Damsal nala, groundwater and mine drainage, like COD, total Fe, TDS, TSS, F, available PO4(-3), available K+ etc., including pH are a serious concerned in this study area.

  13. Pyrolysis Treatment of Chromite Ore Processing Residue by Biomass: Cellulose Pyrolysis and Cr(VI) Reduction Behavior.

    PubMed

    Zhang, Da-Lei; Zhang, Mei-Yi; Zhang, Chu-Hui; Sun, Ying-Jie; Sun, Xiao; Yuan, Xian-Zheng

    2016-03-15

    The pyrolysis treatment with biomass is a promising technology for the remediation of chromite-ore-processing residue (COPR). However, the mechanism of this process is still unclear. In this study, the behavior of pyrolysis reduction of Cr(VI) by cellulose, the main component of biomass, was elucidated. The results showed that the volatile fraction (VF) of cellulose, ie. gas and tar, was responsible for Cr(VI) reduction. All organic compounds, as well as CO and H2 in VF, potentially reduced Cr(VI). X-ray absorption near-edge structure (XANES) spectroscopy and extended X-ray absorption fine-structure (EXAFS) spectroscopy confirmed the reduction of Cr(VI) to Cr(III) and the formation of amorphous Cr2O3. The remnant Cr(VI) content in COPR can be reduced below the detection limit (2 mg/kg) by the reduction of COPR particle and extension of reaction time between VF and COPR. This study provided a deep insight on the co-pyrolysis of cellulose with Cr(VI) in COPR and an ideal approach by which to characterize and optimize the pyrolysis treatment for COPR by other organics.

  14. Pressure increases, the formation of chromite seams, and the development of the ultramafic series in the Stillwater Complex, Montana

    USGS Publications Warehouse

    Lipin, B.R.

    1993-01-01

    This paper explores the hypothesis that chromate seams in the Stillwater Complex formed in response to periodic increases in total pressure in the chamber. Total pressure increased because of the positive ??V of nucleation of CO2 bubbles in the melt and their subsequent rise through the magma chamber, during which the bubbles increased in volume by a factor of 4-6. By analogy with the pressure changes in the summit chambers of Kilauea and Krafla volcanoes, the maximum variation was 0.2-0.25 kbar, or 5-10% of the total pressure in the Stillwater chamber. An evaluation of the likelihood of fountaining and mixing of a new, primitive liquid that entered the chamber with the somewhat more evolved liquid already in the chamber is based upon calculations using observed and inferred velocities and flow rates of basaltic magmas moving through volcanic fissures. The calculations indicate that hot, dense magma would have oozed, rather than fountained into the chamber, and early mixing of the new and residual magmas that could have resulted in chromite crystallizing alone did not take place. -from Author

  15. The differential stress response of adapted chromite mine isolates Bacillus subtilis and Escherichia coli and its impact on bioremediation potential.

    PubMed

    Samuel, Jastin; Paul, Madona Lien; Ravishankar, Harish; Mathur, Ankita; Saha, Dipti Priya; Natarajan, Chandrasekaran; Mukherjee, Amitava

    2013-11-01

    In the current study, indigenous bacterial isolates Bacillus subtilis VITSUKMW1 and Escherichia coli VITSUKMW3 from a chromite mine were adapted to 100 mg L(-1) of Cr(VI). The phase contrast and scanning electron microscopic images showed increase in the length of adapted E. coli cells and chain formation in case of adapted B. subtilis. The presence of chromium on the surface of the bacteria was confirmed by energy dispersive X-ray spectroscopy (EDX), which was also supported by the conspicuous Cr-O peaks in FTIR spectra. The transmission electron microscopic (TEM) images of adapted E. coli and B. subtilis showed the presence of intact cells with Cr accumulated inside the bacteria. The TEM-EDX confirmed the internalization of Cr(VI) in the adapted cells. The specific growth rate and Cr(VI) reduction capacity was significantly higher in adapted B. subtilis compared to that of adapted E. coli. To study the possible role of Cr(VI) toxicity affecting the Cr(VI) reduction capacity, the definite assays for the released reactive oxygen species (ROS) and ROS scavenging enzymes (SOD and GSH) were carried out. The decreased ROS production as well as SOD and GSH release observed in adapted B. subtilis compared to the adapted E. coli corroborated well with its higher specific growth rate and increased Cr(VI) reduction capacity.

  16. Chromate reduction in Fe(II)-containing soil affected by hyperalkaline leachate from chromite ore processing residue.

    PubMed

    Whittleston, Robert A; Stewart, Douglas I; Mortimer, Robert J G; Tilt, Zana C; Brown, Andrew P; Geraki, Kalotina; Burke, Ian T

    2011-10-30

    Highly alkaline (pH 12.2) chromate contaminated leachate (990 μmol L(-1)) has been entering soils below a chromite ore processing residue disposal (COPR) site for over 100 years. The soil immediately beneath the waste has a pH of 11→12.5, contains 0.3→0.5% (w/w) chromium, and 45→75% of the microbially available iron is Fe(II). Despite elevated pH, a viable microbial consortium of Firmicutes dominated iron reducers was isolated from this COPR affected soil. Soil pH and Cr concentration decrease with distance from the waste. XAS analysis of soil samples indicated that Cr is present as a mixed Cr(III)-Fe(III) oxy-hydroxide phase, suggesting that the elevated soil Cr content is due to reductive precipitation of Cr(VI) by Fe(II). Microcosm results demonstrate the capacity of COPR affected soil to abiotically remove all Cr(VI) from the leachate within 40 days. In air oxidation experiments less than 2% of the total Cr in the soil was remobilised despite significant Fe(II) oxidation. XAS analysis after air oxidation showed no change in Cr-speciation, indicating the Cr(III)-containing phase is a stable long term host for Cr. This work suggests that reductive precipitation of Cr(VI) is an effective method of contaminant immobilisation in soils where microbially produced Fe(II) is present.

  17. Effects of particle size and acid addition on the remediation of chromite ore processing residue using ferrous sulfate.

    PubMed

    Jagupilla, Santhi Chandra; Moon, Deok Hyun; Wazne, Mahmoud; Christodoulatos, Christos; Kim, Min Gyu

    2009-08-30

    A bench-scale treatability study was conducted to assess the effects of particle size and acid addition on the remediation of chromite ore processing residue (COPR) using ferrous sulfate. The remediation scheme entailed the chemical reduction of hexavalent chromium [Cr(VI)] and the mitigation of swell potential. Leaching tests and the EQ3/6 geochemical model were used to estimate the acid dosage required to destabilize Cr(VI)-bearing and swell-causing minerals. The model predicted greater acid dosage than that estimated from the batch leaching tests. This indicated that mass transfer limitation may be playing a significant role in impeding the dissolution of COPR minerals following acid addition and hence hindering the remediation of COPR. Cr(VI) concentrations determined by alkaline digestion for the treated samples were less than the current NJDEP standard. However, Cr(VI) concentrations measured by X-ray absorption near edge structure (XANES) were greater than those measured by alkaline digestion. Greater Cr(VI) percentages were reduced for acid pretreated and also for smaller particle size COPR samples. Upon treatment, brownmillerite content was greatly reduced for the acid pretreated samples. Conversely, ettringite, a swell-causing mineral, was not observed in the treated COPR.

  18. Early chromite mining and agricultural clearance: Opportunities for the investigation of agricultural sediment dynamics in the Eastern Piedmont (USA)

    USGS Publications Warehouse

    Bain, D.J.; Brush, G.S.

    2005-01-01

    Many flood plains in the Eastern Piedmont (USA) are buried under deposits of sediment resulting from European agricultural clearance. Classic radioisotopic dating techniques cover temporal periods too short (137Cs, 210Pb) or too long (14C) to reliably date sediments deposited during periods of local European activity (1660-1900). Moreover, many potential biomarkers, such as pollen, degrade in oxic flood plain sediments. In the Baltimore, Maryland (USA) region, early chromite mining (1820 - 1880) occurred during periods of rapid agricultural clearance. Use of chromium (Cr) chemostratigraphic profiles in flood plain sediments tied to historical mining activity can provide improved precision in overbank accumulation rates and timing. Sediment cores were collected from the Red Run basin, which is part of the Baltimore Ecosystem Study, an urban Long-Term Ecological Research site. Trace metal chemostratigraphic profiles were measured and peaks in Cr concentration tied to historic mining activity. Dates from Cr chemostratigraphic profiles were combined with 137Cs dating to reconstruct flood plain sedimentation rates. Red Run early sedimentation rates (1820 - 1880) were higher (0.45 - 1.19 cm/yr) than more recent (1880 - 1963) rates (0.08 - 0.46 cm/yr). This indicates that Piedmont flood plain vertical sediment accumulation might have peaked before the peak in agricultural clearance, earlier than assumed by regional models. The Cr chemostratigraphy is applicable to a wider region including much of the Maryland and Pennsylvania (USA) Piedmont.

  19. Highly doped silicon nanowires by monolayer doping.

    PubMed

    Veerbeek, Janneke; Ye, Liang; Vijselaar, Wouter; Kudernac, Tibor; van der Wiel, Wilfred G; Huskens, Jurriaan

    2017-02-23

    Controlling the doping concentration of silicon nanostructures is challenging. Here, we investigated three different monolayer doping techniques to obtain silicon nanowires with a high doping dose. These routes were based on conventional monolayer doping, starting from covalently bound dopant-containing molecules, or on monolayer contact doping, in which a source substrate coated with a monolayer of a carborane silane was the dopant source. As a third route, both techniques were combined to retain the benefits of conformal monolayer formation and the use of an external capping layer. These routes were used for doping fragile porous nanowires fabricated by metal-assisted chemical etching. Differences in porosity were used to tune the total doping dose inside the nanowires, as measured by X-ray photoelectron spectroscopy and secondary ion mass spectrometry measurements. The higher the porosity, the higher was the surface available for dopant-containing molecules, which in turn led to a higher doping dose. Slightly porous nanowires could be doped via all three routes, which resulted in highly doped nanowires with (projected areal) doping doses of 10(14)-10(15) boron atoms per cm(2) compared to 10(12) atoms per cm(2) for a non-porous planar sample. Highly porous nanowires were not compatible with the conventional monolayer doping technique, but monolayer contact doping and the combined route resulted for these highly porous nanowires in tremendously high doping doses up to 10(17) boron atoms per cm(2).

  20. Use of lanthanum and sulphuric acid to suppress interferences in the flame photometric determination of calcium m soil extracts.

    PubMed

    Evans, C C; Grimshaw, H M

    1968-04-01

    Interference by iron, aluminium and phosphate in the flame photometric determination of calcium in soil extracts is not fully suppressed by lanthanum unless dilute sulphuric acid is also present. The investigation was restricted to the oxy-acetylene flame.

  1. Beam-hardening artifacts on computed tomography images caused by lanthanum carbonate hydrate in a patient on dialysis.

    PubMed

    Hayashi, Hiromitsu; Machida, Minoru; Sekine, Tetsuro; Yamaguchi, Hidenori; Kiriyama, Tomonari; Kumita, Shin-Ichiro

    2010-05-01

    Lanthanum carbonate hydrate is a nonaluminum, noncalcium phosphate binder containing lanthanum (La). It is effective in decreasing the serum phosphate level in patients on dialysis. Because the atomic number of the La contained in lanthanum carbonate hydrate is relatively high, at 57, this agent may cause strong artifacts on computed tomography (CT) images, which may be mistakenly interpreted as foreign bodies. We recently performed CT examination of a patient on Fosrenol chewable tablets (i.e., lanthanum carbonate hydrate). The CT images were difficult to evaluate because of strong beam hardening artifacts, and differentiation from foreign body aspiration was required. We report here our experience and a discussion of the characteristics of this artifact.

  2. A Nodular Foreign Body Reaction in a Dialysis Patient Receiving Long-term Treatment With Lanthanum Carbonate.

    PubMed

    Valika, Aziz K; Jain, Dhanpat; Jaffe, Phillip E; Moeckel, Gilbert; Brewster, Ursula C

    2016-01-01

    A 63-year-old man with HIV (human immunodeficiency virus) infection and end-stage renal disease, treated with lanthanum carbonate phosphate binder for 4 years, presented with anemia and an upper gastrointestinal bleed. Upper endoscopy revealed a nodular hyperplastic epithelium, with an endoscopic ultrasound confirming hyperechoic material within the nodules. Light microscopy showed collections of histiocytes and multinucleated giant cells containing brown granular cytoplasmic material and extracellular crystalline material, a finding confirmed by electron microscopy. Similar pathologic findings associated with lanthanum exposure have been described recently. In our patient, lanthanum carbonate treatment was withdrawn and gastrointestinal bleeding has since ceased. The patient was exposed to a high amount of lanthanum over a long period, which may explain his adverse reaction. However, other contributing factors, such as competing medications or comorbid conditions, also may have increased his sensitivity to the drug.

  3. Solid state interaction studies on binary nitrate mixtures of uranyl nitrate hexahydrate and lanthanum nitrate hexahydrate at elevated temperatures

    NASA Astrophysics Data System (ADS)

    Kalekar, Bhupesh; Raje, Naina; Reddy, A. V. R.

    2017-02-01

    Interaction behavior of uranyl nitrate hexahydrate (UNH) and lanthanum nitrate hexahydrate (LaNH) have been investigated on the mixtures in different molar ratios of the two precursors and monitoring the reactions at elevated temperatures with thermoanalytical and X-ray diffraction measurement techniques. During the decomposition of equimolar mixture of LaNH and UNH, formation of lanthanum uranate (U0.5La0.5)O2, was seen by the temperature of 500 °C along with lanthanum oxide (La2O3) and uranium trioxide (UO3). By the temperature of 700 °C, the formation of uranium sesquioxide (U3O8) was observed along with (U0.5La0.5)O2 as end products in uranium rich mixtures. Lanthanum rich compositions decomposed by the temperature of 700 °C to give (U0.5La0.5)O2 and La2O3 as end products.

  4. Gene doping.

    PubMed

    Azzazy, Hassan M E

    2010-01-01

    Gene doping abuses the legitimate approach of gene therapy. While gene therapy aims to correct genetic disorders by introducing a foreign gene to replace an existing faulty one or by manipulating existing gene(s) to achieve a therapeutic benefit, gene doping employs the same concepts to bestow performance advantages on athletes over their competitors. Recent developments in genetic engineering have contributed significantly to the progress of gene therapy research and currently numerous clinical trials are underway. Some athletes and their staff are probably watching this progress closely. Any gene that plays a role in muscle development, oxygen delivery to tissues, neuromuscular coordination, or even pain control is considered a candidate for gene dopers. Unfortunately, detecting gene doping is technically very difficult because the transgenic proteins expressed by the introduced genes are similar to their endogenous counterparts. Researchers today are racing the clock because assuring the continued integrity of sports competition depends on their ability to develop effective detection strategies in preparation for the 2012 Olympics, which may mark the appearance of genetically modified athletes.

  5. Facile preparation of apatite-type lanthanum silicate by a new water-based sol–gel process

    SciTech Connect

    Yamagata, Chieko; Elias, Daniel R.; Paiva, Mayara R.S.; Misso, Agatha M.; Castanho, Sonia R.H. Mello

    2013-06-01

    Highlights: ► We use a Na{sub 2}SiO{sub 3} waste solution as source of Si. ► We present a simple, rapid and low temperature method of lanthanum silicate apatite preparation. ► TEOS, a high cost reagent, was successfully substituted by a cheap price Na{sub 2}SiO{sub 3}, to obtain pure La{sub 9.56}(SiO{sub 4})6O{sub 2.33} lanthanum silicate apatite. - Abstract: In recent years, apatite-type lanthanum silicates ([Ln{sub 10−x}(XO{sub 4})6O{sub 3–1.5x}] (X = Si or Ge)) have been studied for use in SOFC (solid oxide fuel cells), at low temperature (600–800 °C), due to its ionic conductivity which is higher than that of YSZ (Yttrium Stabilized Zirconia) electrolyte. For this reason they are very promising materials as solid electrolyte for SOFCs. Synthesis of functional nanoparticles is a challenge in the nanotechnology. In this work, apatite-type lanthanum silicate nanoparticles were synthesized by a water-based sol–gel process, i.e., sol–gel technique followed by chemical precipitation of lanthanum hydroxide on the gel of the silica. Na{sub 2}SiO{sub 3} waste solution was used as silica source. Spherical aerogel silica was prepared by acid catalyzed reaction, followed by precipitation of lanthanum hydroxide to obtain the precursor of apatite-type lanthanum silicate. Powders of apatite-type lanthanum silicate achieved from the precursor were characterized by thermal analysis, X-ray diffraction (XRD), scanning electron microscopy (SEM) and specific surface area measurements (BET). The apatite phase was formed at 900 °C.

  6. Magnetic properties of pure and Fe doped HoCrO3 thin films fabricated via a solution route

    NASA Astrophysics Data System (ADS)

    Yin, Shiqi; Sauyet, Theodore; Guild, Curt; Suib, S. L.; Jain, Menka

    2017-04-01

    Multiferroic properties of orthorhombically distorted perovskite rare-earth chromites, such as HoCrO3, are being investigated extensively in recent years. In the present work, we report on the effect of Fe substitution on the magnetic properties of HoCrO3 thin films. Thin films of HoCrO3 and HoCr0.7Fe0.3O3 were fabricated via a solution route on platinized silicon substrates. Structural properties of the films were evaluated by X-ray diffraction and Raman spectroscopy techniques. The surface morphology and cross-sections of the films were examined using scanning electron microscopy. Optical band gaps of pure and Fe doped HoCrO3 films are found to be 3.45 eV and 3.39 eV, respectively. The magnetization measurements show that the Néel temperatures (where Cr3+ orders) for the HoCrO3 and HoCr0.7Fe0.3O3 films are 134 and 148 K, respectively. In a magnetic field of 2 T, the maximum entropy change and relative cooling power, two parameters to evaluate the magnetocaloric properties of a material, were 0.813 J/kg K at 11 K and 21.1 J/kg for HoCrO3 film, in comparison with 0.748 J/kg K at 15 K and 26.8 J/kg for HoCr0.7Fe0.3O3 film. To our knowledge, this is the first work exploring the band gap and magnetocaloric properties of rare-earth chromite thin films. These findings should inspire the development of rare-earth chromite thin films for temperature control of nanoscale electronic devices and sensors in the low temperature region (< 30 K).

  7. Remediation of hexavalent chromium contamination in chromite ore processing residue by sodium dithionite and sodium phosphate addition and its mechanism.

    PubMed

    Li, Yunyi; Cundy, Andrew B; Feng, Jingxuan; Fu, Hang; Wang, Xiaojing; Liu, Yangsheng

    2017-05-01

    Large amounts of chromite ore processing residue (COPR) wastes have been deposited in many countries worldwide, generating significant contamination issues from the highly mobile and toxic hexavalent chromium species (Cr(VI)). In this study, sodium dithionite (Na2S2O4) was used to reduce Cr(VI) to Cr(III) in COPR containing high available Fe, and then sodium phosphate (Na3PO4) was utilized to further immobilize Cr(III), via a two-step procedure (TSP). Remediation and immobilization processes and mechanisms were systematically investigated using batch experiments, sequential extraction studies, X-ray diffraction (XRD) and X-ray Photoelectron Spectroscopy (XPS). Results showed that Na2S2O4 effectively reduced Cr(VI) to Cr(III), catalyzed by Fe(III). The subsequent addition of Na3PO4 further immobilized Cr(III) by the formation of crystalline CrPO4·6H2O. However, addition of Na3PO4 simultaneously with Na2S2O4 (via a one-step procedure, OSP) impeded Cr(VI) reduction due to the competitive reaction of Na3PO4 and Na2S2O4 with Fe(III). Thus, the remediation efficiency of the TSP was much higher than the corresponding OSP. Using an optimal dosage in the two-step procedure (Na2S2O4 at a dosage of 12× the stoichiometric requirement for 15 days, and then Na3PO4 in a molar ratio (i.e. Na3PO4: initial Cr(VI)) of 4:1 for another 15 days), the total dissolved Cr in the leachate determined via Toxicity Characteristic Leaching Procedure (TCLP Cr) testing of our samples was reduced to 3.8 mg/L (from an initial TCLP Cr of 112.2 mg/L, i.e. at >96% efficiency).

  8. Bio-concentration of chromium--an in situ phytoremediation study at South Kaliapani chromite mining area of Orissa, India.

    PubMed

    Mohanty, Monalisa; Pattnaik, Mausumi M; Mishra, Aruna K; Patra, Hemanta K

    2012-01-01

    Mine waste water at South Kaliapani usually contains toxic levels of hexavalent Cr(VI). The present in situ study was conducted at South Kaliapani chromite mine area in Orissa state, India, to assess the phytoremediation ability of three plants, namely, rice (Oryza sativa L.), paragrass (Brachiaria mutica), and an aquatic weed (Eichhornia crassipes), in attenuating Cr(VI) from mine waste water and to correlate the bio-concentration factors (BCF) of Cr. Water hyacinth (E. crassipes) showed 24% to 54% reduction whereas paragrass (B. mutica) was able to reduce 18% to 33% of Cr(VI) from mine water. This reduction was studied over a period of 100 days of plant growth. The reduction was observed through a passage of a sum total of 2,000 sq. ft. cultivated plots and ponds separately. Reduction in Cr(VI) content in mine water varies with plant age as well as with the distance of passage. Cr accumulation and BCF values increased with high soil Cr levels as well as the age of plants. High BCF and transportation index (Ti) values, i.e., 10,924 and 32.09, respectively, were noted for water hyacinth. The Ti values indicated that the root-to-shoot translocation of Cr was very high after 100 days of growth. The total accumulation rate was maximum (8.29 mg Cr kg dry biomass(-1) day (-1)) in paragrass. The BCF values for roots were noted to be higher than those of leaves, stems, and grains of the 125-day-old plants. Hence, paragrass and water hyacinth may be used as tools of phytoremediation to combat the problem of in situ Cr contamination.

  9. Magnetization reversal behavior and magnetocaloric effect in SmCr0.85Mn0.15O3 chromites

    NASA Astrophysics Data System (ADS)

    Kumar, Surendra; Coondoo, Indrani; Vasundhara, M.; Patra, Ajit K.; Kholkin, Andrei L.; Panwar, Neeraj

    2017-01-01

    We have synthesized SmCr0.85Mn0.15O3 (SCMO) chromites through the ceramic route. The compound crystallized into a distorted orthorhombic structure with the Pnma space group, which was confirmed from the Rietveld refinement of x-ray powder diffraction patterns. Neel temperature, noticed at 168 K from the temperature variation of magnetisation, smaller than that reported for SmCrO3, indicated the influence of Mn3+ substitution on decreasing the antiferromagnetic ordering. A phenomenon of magnetization reversal was observed in the SCMO compound. At low magnetic fields, i.e., 500 Oe, a single compensation temperature (defined as the temperature where magnetization became zero) around 106 K was observed in the field cooled magnetization curve. However, with the application of higher magnetic fields, i.e., under an applied field of 1000 Oe, a second compensation temperature was noticed around 8 K. With a further increase in the magnetic field, the magnetization remained positive in both field cooled and zero field cooled protocols. A normal magnetocaloric effect was observed through an indirect method of field dependence of magnetisation measured in the temperature range of 2-152 K. The magnetic entropy change (-ΔS) of ˜11.36 J kg-1 K-1 along with the relative cooling power (RCP) of ˜175.89 J kg-1 was obtained in the temperature range of 10-20 K for an applied field of 90 kOe, and their values at 50 kOe applied field were, respectively, almost twenty and forty times larger in magnitude in comparison to those for the SmCrO3 compound. The relatively large values of ΔS and RCP make the studied compound a potential candidate for magnetic refrigeration applications at low temperatures.

  10. Urinary excretion of chromium following ingestion of chromite-ore processing residues in humans: implications for biomonitoring.

    PubMed

    Gargas, M L; Norton, R L; Harris, M A; Paustenbach, D J; Finley, B L

    1994-12-01

    Biomonitoring programs for urinary chromium (Cr) typically attempt to evaluate occupational exposure via the inhalation route. This study investigated whether Cr can be detected in the urine of people following the ingestion of soils that contain relatively high concentrations of chromium in chromite ore processing residue (COPR). To evaluate the reasonableness of using urinary monitoring to assess environmental exposure, six volunteers ingested 400 mg of soil/day (low-dose group), two others ingested 2.0 g of soil/day (high-dose group) for 3 consecutive days, and one person ingested a placebo on each of 3 days. The soil and COPR mixture contained concentrations of total chromium (Cr) and hexavalent chromium [Cr(VI)] of 103 +/- 20 and 9.3 +/- 3.8 mg/kg, respectively. Therefore, the low-dose group ingested 41 micrograms Cr/day [including 3.7 micrograms Cr(VI)] and the high-dose group ingested 206 micrograms Cr/day [including 18.6 micrograms Cr(VI)] on each of 3 consecutive days. All urine samples were collected and analyzed individually for total Cr on the day prior to dosing, during the 3 days of dosing, and up to the first void 48 h after the last dose. No significant increases in urinary Cr excretion were found when background excretion data were compared with data following each of the 3 days of dosing or in daily mean urine concentrations of the high- vs the low-dose groups. It appears that Cr present in a soil and COPR mixture at Cr doses up to 200 micrograms/day is not sufficiently bioavailable for biomonitoring of urine to be informative.(ABSTRACT TRUNCATED AT 250 WORDS)

  11. Pilot scale treatment of chromite ore processing residue using sodium sulfide in single reduction and coupled reduction/stabilization processes.

    PubMed

    Velasco, Antonio; Ramírez, Martha; Hernández, Sergio; Schmidt, Winfried; Revah, Sergio

    2012-03-15

    Single Cr(VI) reduction and coupled reduction/stabilization (R/S) processes were evaluated at pilot scale to determine their effectiveness to treat chromite ore processing residue (COPR). Sodium sulfide was used as the reducing agent and cement, gypsum and lime were tested as the stabilizing agents. The pilot experiments were performed in a helical ribbon blender mixer with batches of 250 kg of COPR and mixing time up to 30 min. Na2S/Cr(VI) mass ratios of 4.6, 5.7 and 6.8 were evaluated in the single reduction process to treat COPR with Cr(VI) concentration of ≈4.2 g/kg. The R/S process was tested with a Na2S/Cr(VI) mass ratio of 5.7 and including stabilizing agents not exceeding 5% (w/w(COPR)), to treat COPR with a Cr(VI) content of ≈5.1g/kg. The single reduction process with a ratio of 6.8, reached Cr(VI) reduction efficiencies up to 97.6% in the first days, however these values decreased to around 93% after 380 days of storage. At this point the total Cr level was around 12.5 mg/L. Cr(VI) removal efficiencies exceeding 96.5% were reached and maintained during 380 days when the coupled R/S process was evaluated. Total Cr levels lower than 5 mg/l were attained at the initials days in all R/S batch tested, however after 380 days, concentrations below the regulatory limit were only found with gypsum (2%) as single agent and with a blend of cement (4%) and lime (1%). These results indicated that the coupled R/S process is an excellent alternative to stabilize COPR.

  12. A Russian record of a Middle Ordovician meteorite shower: Extraterrestrial chromite at Lynna River, St. Petersburg region

    NASA Astrophysics Data System (ADS)

    Lindskog, Anders; Schmitz, Birger; Cronholm, Anders; Dronov, Andrei

    2012-08-01

    Numerous fossil meteorites and high concentrations of sediment-dispersed extraterrestrial chromite (EC) grains with ordinary chondritic composition have previously been documented from 467 ± 1.6 Ma Middle Ordovician (Darriwilian) strata. These finds probably reflect a temporarily enhanced influx of L-chondritic matter, following the disruption of the L-chondrite parent body in the asteroid belt 470 ± 6 Ma. In this study, a Volkhovian-Kundan limestone/marl succession at Lynna River, northwestern Russia, has been searched for EC grains (>63 μm). Eight samples, forming two separate sample sets, were collected. Five samples from strata around the Asaphus expansus-A. raniceps trilobite Zone boundary, in the lower-middle Kundan, yielded a total of 496 EC grains in 65.5 kg of rock (average 7.6 EC grains kg-1, but up to 10.2 grains kg-1). These are extremely high concentrations, three orders of magnitude higher than "background" levels in similar condensed sediment from other periods. EC grains are typically about 50 times more abundant than terrestrial chrome spinel in the samples and about as common as terrestrial ilmenite. Three stratigraphically lower lying samples, close to the A. lepidurus-A. expansus trilobite Zone boundary, at the Volkhov-Kunda boundary, yielded only two EC grains in 38.2 kg of rock (0.05 grains kg-1). The lack of commonly occurring EC grains in the lower interval probably reflects that these strata formed before the disruption of the L-chondrite parent body. The great similarity in EC chemical composition between this and other comparable studies indicates that all or most EC grains in these Russian mid-Ordovician strata share a common source--the L-chondrite parent body.

  13. Rapid dissolution of chromite with sulphuric acid-lithium sulphate mixture containing ceric sulphate, manganese dioxide or periodate, and spectrophotometric determination of chromium.

    PubMed

    Yoshikuni, N

    1991-05-01

    Cr(2)O(3) and chromite ore can be dissolved in H(2)SO(4)Li(2)SO(4)Ce(SO(4))(2) (20/10/1 v/w/w), H(2)SO(4)Li(2)SO(4)MnO(2) (20/10/1 v/w/w) and H(2)SO(4)Li(2)SO(4)KIO(4) (20/10/2 v/w/w) mixtures. The turbid solution produced can be clarified by treatment with H(2)O(2) or solvent extraction and the chromium determined spectrophotometrically at 614 nm.

  14. The lanthanum gallate-based mixed conducting perovskite ceramics

    NASA Astrophysics Data System (ADS)

    Politova, E. D.; Stefanovich, S. Yu.; Aleksandrovskii, V. V.; Kaleva, G. M.; Mosunov, A. V.; Avetisov, A. K.; Sung, J. S.; Choo, K. Y.; Kim, T. H.

    2005-01-01

    The structure, microstructure, dielectric, and transport properties of the anion deficient perovskite solid solutions (La,Sr)(Ga,Mg,M)O3- with M=Fe, Ni have been studied. Substitution of iron and nickel for gallium up to about 20 and 40 at.% respectively, leads to the perovskite lattice contraction due to the cation substitutions by the transition elements. The transition from pure ionic to mixed ionic-electronic conductivity was observed for both the systems studied. Both the enhancement of total conductivity and increasing in the thermal expansion coefficient values has been proved to correlate with the increasing amount of weakly bounded oxygen species in the Fe or Ni-doped ceramics. The oxygen ionic conductivity has been estimated from the kinetic experiments using the dc-conductivity and dilatometry methods under the condition of the stepwise change of the atmosphere from nitrogen to oxygen.

  15. Lanthanum carbonate oral powder: satisfaction, preference and adherence in French and Spanish patients with end-stage renal disease

    PubMed Central

    Keith, Michael; de Sequera, Patricia; Clair, François; Pedersini, Riccardo

    2016-01-01

    Background Phosphate binders, such as lanthanum carbonate, control elevated serum-phosphate levels in patients with end-stage renal disease (ESRD). Lanthanum carbonate is available in oral powder and tablet form. The aim of this survey was to investigate satisfaction with, preference for, and adherence to lanthanum carbonate oral powder in patients with ESRD. Scope Patients from France and Spain who had been taking lanthanum carbonate powder for at least 4 weeks, and who had experience of other phosphate binders of any formulation, were asked to complete an online or telephone survey. Treatment satisfaction was measured using the Treatment Satisfaction Questionnaire for Medication-9; preference was measured using 5-point Likert scale agreement ratings; and adherence was measured using the Morisky Medication Adherence Scale-4. Data were evaluated using bivariate analyses. Findings Overall, 160 patients participated (80 per country). Lanthanum carbonate powder was reported to have a higher effectiveness rating (p<0.05), be more convenient (p<0.05), and provide a higher level of satisfaction (p<0.01) than previous binders. There was an overall preference for lanthanum carbonate powder over previous binders of any formulation (p<0.001). Adherence to medication was similar for all binders analysed: 66.3% of French patients adhered to lanthanum carbonate powder, and 65.0% adhered to previous binder treatment (p=not significant); 52.5% of Spanish patients adhered to lanthanum carbonate powder, and 56.3% adhered to previous binder treatment (p=not significant). Limitations The survey enrolled patients who had already experienced phosphate binders before the study began. Information on patient preferences for and adherence to previous phosphate binders was therefore based on the patients’ memories of these experiences, which may have been subject to change over time. Although most participants completed the online survey in this study, a telephone survey was used for

  16. High-efficiency, low-temperature cesium diodes with lanthanum-hexaboride electrodes

    NASA Technical Reports Server (NTRS)

    Morris, J. F.

    1974-01-01

    Lanthanum-hexaboride electrodes in 1700 K cesium diodes may triple power outputs compared with those demonstrated for nuclear thermionic space applications. Still greater relative gains seem possible for emitters below 1700 K. Further improvements in cesium-diode performance should result from the lower collector temperatures allowed for earth and low-power-space duties. Decreased temperatures will lessen thermal-transport losses that attend thermionic-conversion mechanisms. Such advantages will add to those from collector-Carnot and electrode effects. If plasma ignition difficulties impede diode temperature reductions, recycling small fractions of the output power could provide ionization. So high-efficiency, low-temperature cesium diodes with lanthanum-hexaboride electrodes appear feasible.

  17. Near fifty percent sodium substituted lanthanum manganites—A potential magnetic refrigerant for room temperature applications

    SciTech Connect

    Sethulakshmi, N.; Anantharaman, M. R.; Al-Omari, I. A.; Suresh, K. G.

    2014-03-03

    Nearly half of lanthanum sites in lanthanum manganites were substituted with monovalent ion-sodium and the compound possessed distorted orthorhombic structure. Ferromagnetic ordering at 300 K and the magnetic isotherms at different temperature ranges were analyzed for estimating magnetic entropy variation. Magnetic entropy change of 1.5 J·kg{sup −1}·K{sup −1} was observed near 300 K. An appreciable magnetocaloric effect was also observed for a wide range of temperatures near 300 K for small magnetic field variation. Heat capacity was measured for temperatures lower than 300 K and the adiabatic temperature change increases with increase in temperature with a maximum of 0.62 K at 280 K.

  18. Lanthanum(III) and praseodymium(III) derivatives with dithiocarbamates derived from alpha-amino acids.

    PubMed

    Rai, Anita; Sengupta, Soumitra K; Pandey, Om P

    2006-06-01

    Lanthanum(III) and praseodymium(III) complexes with dithiocarbamates have been synthesized by the reactions of lanthanum(III) and praseodymium(III) chloride with barium dithiocarbamate and complexes of type [LnCl(L)H2O]n have been obtained (where Ln=La(III) or Pr(III); L=barium salt of dithiocarbamate derived from glycine, L-leucine, L-valine, DL-alanine). The complexes have been characterized by elemental analysis, molar conductance, electronic absorption and fluorescence, infrared, far infrared, 1H NMR spectral studies. The presence of coordinated water molecule is inferred from thermogravimetric analysis which indicates the loss of one water molecule at 150-170 degrees C. The oscillator strength, Judd-Ofelt intensity parameter, stimulated emission cross-section, etc. have been obtained for different transitions of Pr3+.

  19. Sorption of tartrate ions to lanthanum (III)-modified calcium fluor- and hydroxyapatite.

    PubMed

    Aissa, Abdallah; Debbabi, Mongi; Gruselle, Michel; Thouvenot, René; Flambard, Alexandrine; Gredin, Patrick; Beaunier, Patricia; Tõnsuaadu, Kaia

    2009-02-01

    The present article details the formation of lanthanum-modified apatites and the binding process of tartrate ions with these obtained apatites. Chemical analyses, FT-IR and (31)P NMR spectroscopies, XRD powder, TGA, and TEM analyses were employed for studying the reaction between Ca(10)(PO(4))(6)(OH)(2) (HAp) or Ca(10)(PO(4))(6)(F)(2) (FAp) and LaCl(3). The reaction was found to take place mainly through partial dissolution of the apatite followed by precipitation of a new phase containing lanthanum phosphate. When La(3+) was introduced in the presence of L(+)-tartaric acid (TAH(2)), no fundamental changes were observed in the HAp or FAp structures. However, there did occur a formation of a new phase of Ca or/and La tartrate salt.

  20. Sensitive and reliable ascorbic acid sensing by lanthanum oxide/reduced graphene oxide nanocomposite.

    PubMed

    Mogha, Navin Kumar; Sahu, Vikrant; Sharma, Meenakshi; Sharma, Raj Kishore; Masram, Dhanraj T

    2014-10-01

    A simple strategy for the detection and estimation of ascorbic acid (AA), using lanthanum oxide-reduced graphene oxide nanocomposite (LO/RGO) on indium tin oxide (ITO) substrate, is reported. LO/RGO displays high catalytic activity toward the oxidation of AA, and the synergism between lanthanum oxide and reduced graphene oxide was attributed to the successful and efficient detection. Detection mechanism and sensing efficacy of LO/RGO nanocomposite are investigated by electrochemical techniques. Chronoamperometric results under optimal conditions show a linear response range from 14 to 100 μM for AA detection. Commercially available vitamin C tablets were also analyzed using the proposed LO/RGO sensor, and the remarkable recovery percentage (97.64-99.7) shows the potential application in AA detection.

  1. Measurement of lanthanum and technetium in uranium fuels by inductively coupled plasma atomic emission spectroscopy.

    SciTech Connect

    Carney, K.; Crane, P.; Cummings, D.; Krsul, J.; McKnight, R.

    1999-06-10

    An important parameter in characterizing an irradiated nuclear fuel is determining the amount of uranium fissioned. By determining the amount of uranium fissioned in the fuel a burnup performance parameter can be calculated, and the amount of fission products left in the fuel can be predicted. The quantity of uranium fissioned can be calculated from the amount of lanthanum and technetium present in the fuel. Lanthanum and technetium were measured in irradiated fuel samples using an Inductively Coupled Plasma Atomic Emission Spectroscopy (ICP-AES) instrument and separation equipment located in a shielded glove-box. A discussion of the method, interferences, detection limits, quality control and a comparison to other work will be presented.

  2. Investigation of band gap narrowing in nitrogen-doped La2Ti2O7 with transient absorption spectroscopy.

    PubMed

    Yost, Brandon T; Cushing, Scott K; Meng, Fanke; Bright, Joeseph; Bas, Derek A; Wu, Nianqiang; Bristow, Alan D

    2015-12-14

    Doping a semiconductor can extend the light absorption range, however, it usually introduces mid-gap states, reducing the charge carrier lifetime. This report shows that doping lanthanum dititinate (La2Ti2O7) with nitrogen extends the valence band edge by creating a continuum of dopant states, increasing the light absorption edge from 380 nm to 550 nm without adding mid-gap states. The dopant states are experimentally resolved in the excited state by correlating transient absorption spectroscopy with a supercontinuum probe and DFT prediction. The lack of mid-gap states is further confirmed by measuring the excited state lifetimes, which reveal the shifted band edge only increased carrier thermalization rates to the band edge and not interband charge recombination under both ultraviolet and visible excitation. Terahertz (time-domain) spectroscopy also reveals that the conduction mechanism remains unchanged after doping, suggesting the states are delocalized.

  3. Time-resolved Langmuir Probing of a New Lanthanum Hexaboride (LaB6) Hollow Cathode

    DTIC Science & Technology

    2011-09-01

    like texture and is easily machineable with standard tooling. Competing thermally conductive but electrically insulating ceramics such as aluminum...The 32nd International Electric Propulsion Conference, Wiesbaden, Germany September 11 – 15, 2011 1 Time-resolved Langmuir Probing of a New...Lanthanum Hexaboride (LaB6) Hollow Cathode IEPC-2011-245 Presented at the 32nd International Electric Propulsion Conference, Wiesbaden

  4. Chromium and copper substituted lanthanum nano-ferrites: Their synthesis, characterization and application studies

    NASA Astrophysics Data System (ADS)

    Jauhar, Sheenu; Singhal, Sonal

    2014-10-01

    Nano-crystalline lanthanum ferrites substituted by chromium and copper having formula LaMxFe1-xO3 (M = Cr, Cu; 0.0 ⩽ x ⩽ 0.5) were synthesized using sol-gel auto-combustion method. The formation of ferrite particles was confirmed using Fourier Transform Infra-Red (FT-IR) spectra and powder X-ray Diffraction (XRD) techniques. The entire ferrite compositions were found to be pure phased with same symmetry as LaFeO3. The average crystallite size was calculated to be ∼60 nm. The ferrite compositions were observed to behave as semi-conductors, as their resistivity decreased with increasing temperature. These ferrite compositions were employed as catalysts in the decomposition of hydrogen peroxide solution (0.17 M). Pure LaFeO3 was found to have a very low catalytic activity towards the decomposition of hydrogen peroxide solution, while presence of copper in the lanthanum ferrite lattice was found to significantly enhance its catalytic activity. The rate constant in case of reactions catalysed by LaCu0.5Fe0.5O3 was nearly 25 times larger than that obtained from reactions catalysed by pure LaFeO3. However, chromium substitution was not found to influence the catalytic activity of lanthanum ferrites as chromium substituted lanthanum ferrites exhibited very low catalytic activity. This was explained on the basis of relative stability of oxidation states of the substituent ions and the presence of defects in the crystal lattice.

  5. Effect of chloride incorporation on the crystallization of zirconium-barium-lanthanum-aluminum fluoride glass

    NASA Technical Reports Server (NTRS)

    Neilson, G. F.; Smith, G. L.; Weinberg, M. C.

    1985-01-01

    One aspect of the influence of preparation procedure on the crystallization behavior of a zirconium-barium-lanthanum-aluminum fluoride glass was studied. The crystallization pattern of this glass may be affected by the chlorine concentration within it. In particular, when such glasses are heated at low temperatures, the alpha-Ba-Zr-F6 crystalline phase forms only in those glasses which contain chloride.

  6. Ca2+-Doped CeBr3 Scintillating Materials

    SciTech Connect

    Guss, Paul; Foster, Michael E.; Wong, Bryan M.; Doty, F. Patrick; Shah, Kanai; Squillante, Michael R.; Shirwadkar, Urmila; Hawrami, Rastgo; Tower, Josh; Yuan, Ding

    2014-01-01

    Despite the outstanding scintillation performance characteristics of cerium tribromide (CeBr3) and cerium-activated lanthanum tribromide, their commercial availability and application are limited due to the difficulties of growing large, crack-free single crystals from these fragile materials. This investigation employed aliovalent doping to increase crystal strength while maintaining the optical properties of the crystal. One divalent dopant (Ca2+) was used as a dopant to strengthen CeBr3 without negatively impacting scintillation performance. Ingots containing nominal concentrations of 1.9% of the Ca2+ dopant were grown. Preliminary scintillation measurements are presented for this aliovalently doped scintillator. Ca2+-doped CeBr3 exhibited little or no change in the peak fluorescence emission for 371 nm optical excitation for CeBr3. The structural, electronic, and optical properties of CeBr3 crystals were studied using the density functional theory within the generalized gradient approximation. The calculated lattice parameters are in good agreement with the experimental data. The energy band structures and density of states were obtained. The optical properties of CeBr3, including the dielectric function, were calculated.

  7. Lanthanum carbonate reduces urine phosphorus excretion: evidence of high-capacity phosphate binding.

    PubMed

    Pennick, Michael; Poole, Lynne; Dennis, Kerry; Smyth, Michael

    2012-01-01

    The effectiveness of phosphate binders can be assessed by evaluating urinary phosphorus excretion in healthy volunteers, which indicates the ability of the phosphate binder to reduce gastrointestinal phosphate absorption. Healthy volunteers were enrolled into one of five separate randomized trials; four were open label and one double blind. Following a screening period of ≤28 days, participants received differing tablets containing lanthanum carbonate [LC, 3000 mg/day of elemental lanthanum (in one study other doses were also used)]. Participants received a standardized phosphate diet and remained in the relevant study center throughout the duration of each treatment period. The end point in all studies was the reduction in urinary phosphorus excretion. Reductions in mean 24-h urinary phosphorus excretion in volunteers receiving a lanthanum dose of 3000 mg/day were between 236 and 468 mg/day over the five separate studies. These data in healthy volunteers can be used to estimate the amount of reduction of dietary phosphate absorption by LC. The reduction in 24-h urinary phosphorus excretion per tablet was compared with published data on other phosphate binders. Although there are limitations, evidence suggests that LC is a very effective phosphate binder in terms of binding per tablet.

  8. Multicenter study of long-term (two-year) efficacy of lanthanum carbonate.

    PubMed

    Ando, Ryoichi; Kimura, Hitoshi; Sato, Hidehiko; Iwamoto, Shunsuke; Yoshizaki, Yuki; Chida, Yoshiko; Ishida, Yuji; Takayama, Masanobu; Yamada, Kouei; Tachibana, Ken; Ohtsuka, Masakazu; Kikuchi, Kan; Inoue, Atsushi

    2013-04-01

    Long-term efficacy of lanthanum carbonate on hyperphosphatemia was examined in multicenter dialysis patients. Outcome and efficacy after 2 years was investigated in 101 patients who had undergone lanthanum carbonate administration. Thirty-three cases dropped out by the 2-year point; patients undergoing at least 2 years of administration totaled 68. Reasons for dropping out were as follows: improvement of hyperphosphatemia, nine cases; changing hospitals, seven cases; medical complications, five cases; digestive symptoms, four cases; poor compliance, four cases; parathyroidectomy, two cases; death, two cases. The mean dosage was increased from initial daily dosage of 744 mg to 1266 mg after 1 year, and to 1246 mg after 2 years. Serum phosphate concentration decreased significantly from the initial 6.15 mg to 5.57 mg/dL after 1 year, and to 5.45 mg/dL after 2 years. Although a lowering trend was observed in corrected calcium levels, the difference was not significant. Parathyroid hormone was unchanged. Achievement rate of Japanese Society for Dialysis Therapy (JSDT) management target values for both phosphorus and calcium improved from 32.7% to 50.0% after 1 year, and to 56.5% after 2 years. Lanthanum carbonate is useful as a therapeutic tool for hyperphosphatemia over long durations.

  9. Impact of lanthanum carbonate on cortical bone in dialysis patients with adynamic bone disease.

    PubMed

    Yajima, Aiji; Inaba, Masaaki; Tominaga, Yoshihiro; Tanaka, Motoko; Otsubo, Shigeru; Nitta, Kosaku; Ito, Akemi; Satoh, Shigeru

    2013-04-01

    Among the most serious problems in patients with chronic kidney disease (CKD) is fragility of cortical bone caused by cortical thinning and increased cortical porosity; the cortical fragility is sometimes irreversible, with fractures generally initiating from cortical bone. Therefore, development of treatments for problems of cortical bone is urgently desired. Cortical bone has the three surfaces, including the periosteal surface, intracortical spaces and endocortical surface. Bone turnover at the endocortical surface and intracortical resorption spaces are increased as compared with that at cancellous surface. Bone growth sometimes depends on apposition at the periosteal surface. We treated hyperphosphatemia in two hemodialysis patients with adynamic bone disease with 750-1500 mg/day of lanthanum carbonate, which is a non-calcium containing phosphate binder; the treatment resulted in a decrease of the serum phosphorus levels (P levels), without significant change of the serum intact parathyroid hormone levels. We now report that treatment of these patients with lanthanum carbonate increased mineralization of the periosteal surface, increased bone mass within the intracortical resorption spaces and increased mineralization of the minimodeling surface at the endocortical surface. In addition, woven bone volume in cortical bone was decreased and mineralization of bone units, namely, osteons, was increased. Although these findings were not observed across all surfaces of the cortical bone in the patients, it is expected that lanthanum carbonate would increase the cortical stability in CKD patients, with consequent reduction in the fracture rate in these patients.

  10. Efficacy of continuous oral administration of lanthanum carbonate over 24 months.

    PubMed

    Ishizu, Takashi; Hong, Zhang; Matsunaga, Tsuneaki; Kaneko, Yoko; Taru, Yoshinori

    2013-04-01

    To examine the efficacy of long-term administration of lanthanum carbonate, changes in serum Ca, phosphate, whole parathyroid hormone (wPTH), and ALP were examined in 40 patients who were able to tolerate dosage of lanthanum carbonate over a continuous period of 24 months. Concurrently, concomitant administration of other phosphate binders, cinacalcet, vitamin D, etc., was also examined. After 24 months, serum phosphorus levels (P levels) had decreased to within management target of guidelines, from 6.16 ± 1.44 mg/dL to 5.58 ± 1.15 mg/dL, and this effect was maintained for 2 years. There were no changes in Ca level. wPTH did not change significantly but tended to increase at 12 months. The dose of concomitantly administered calcium carbonate and sevelamer hydrochloride was reduced. The P-lowering function of lanthanum carbonate still held steady at 24 months following the start of dosage. Because of the rising trend seen in wPTH, dose of cinacalcet and/or vitamin D need to be modulated. Reducing the number of concomitantly administered phosphate binder tablets was desirable from the standpoint of patient adherence.

  11. The kinetics of uptake and recovery of lanthanum using freshwater algae as biosorbents: comparative analysis.

    PubMed

    Birungi, Z S; Chirwa, E M N

    2014-05-01

    In this study, the adsorption and desorption kinetics of lanthanum (La) on micro algal cells was investigated. The internal transcribed spacer (ITS) and 18S ribosomal RNA gene (rRNA) were used for molecular identification of the species. The algal species were found to have 95-98% identities to Desmodesmus multivariabilis, Scenedesmus acuminutus, Chloroidium saccharophilum and Stichococcus bacillaris. The species were cultured and tested independently. D. multivariabilis was found to be the most efficient at adsorbing lanthanum with a maximum sorption capacity (qmax) of 100 mg/g and a high affinity (b) of 4.55 L/g. Desorption of La was also highest in D. multivariabilis with recovery up to 99.63% at initial concentration as high as 100 mg/L. Desorption data fitted best to the modified pseudo second-order with a better correlation coefficient (R(2)) of ⩽0.98 than first order model. The results showed feasibility of lanthanum recovery using algal sorbents, a cost effective method.

  12. Mass-analyzed threshold ionization of an excited state of lanthanum dioxide

    NASA Astrophysics Data System (ADS)

    Wu, Lu; Liu, Yang; Zhang, Changhua; Li, Shenggang; Dixon, David A.; Yang, Dong-Sheng

    2012-07-01

    LaO2 was produced in a pulsed laser-vaporization molecular beam source and studied by mass-analyzed threshold ionization (MATI) spectroscopy and ab initio electronic structure calculations. The calculations included density functional theory, second-order perturbation theory, coupled cluster theory, and complete active space self-consistent field methods. The adiabatic ionization energy of the molecule and vibrational frequencies of the molecule and its cation were measured accurately for the first time from the MATI spectrum. Numerous ionization processes of lanthanum dioxide, peroxide, and superoxide were considered; the 3B2 ← 4B2 electronic transition of the dioxide was assigned upon comparison with the observed spectrum. The ionization energy and O-La-O bending frequency of the 4B2 neutral state are 4.9760 (6) eV and 92 cm-1, respectively. The La-O stretching and O-La-O bending frequencies of the 3B2 cationic state are 656 and 122 cm-1, respectively. The 4B2 state is formed by two electron transfer from lanthanum to oxygen atoms, and the 3B2 state is produced by the further removal of a lanthanum 6s-based electron.

  13. Preparation and Characterization of Lanthanum-Incorporated Hydroxyapatite Coatings on Titanium Substrates

    PubMed Central

    Lou, Weiwei; Dong, Yiwen; Zhang, Hualin; Jin, Yifan; Hu, Xiaohui; Ma, Jianfeng; Liu, Jinsong; Wu, Gang

    2015-01-01

    Titanium (Ti) has been widely used in clinical applications for its excellent biocompatibility and mechanical properties. However, the bioinertness of the surface of Ti has motivated researchers to improve the physicochemical and biological properties of the implants through various surface modifications, such as coatings. For this purpose, we prepared a novel bioactive material, a lanthanum-incorporated hydroxyapatite (La-HA) coating, using a dip-coating technique with a La-HA sol along with post-heat treatment. The XRD, FTIR and EDX results presented in this paper confirmed that lanthanum was successfully incorporated into the structure of HA. The La-HA coating was composed of rod-like particles which densely compacted together without microcracks. The results of the interfacial shear strength test indicated that the incorporation of lanthanum increased the bonding strength of the HA coating. The mass loss ratios under acidic conditions (pH = 5.5) suggested that the La-HA coatings have better acid resistance. The cytocompatibility of the La-HA coating was also revealed by the relative activity of alkaline phosphatase, cellular morphology and cell proliferation assay in vitro. The present study suggested that La-HA coated on Ti has promising potential for applications in the development of a new type of bioactive coating for metal implants. PMID:26404255

  14. Lanthanum halide scintillators for time-of-flight 3-D pet

    DOEpatents

    Karp, Joel S.; Surti, Suleman

    2008-06-03

    A Lanthanum Halide scintillator (for example LaCl.sub.3 and LaBr.sub.3) with fast decay time and good timing resolution, as well as high light output and good energy resolution, is used in the design of a PET scanner. The PET scanner includes a cavity for accepting a patient and a plurality of PET detector modules arranged in an approximately cylindrical configuration about the cavity. Each PET detector includes a Lanthanum Halide scintillator having a plurality of Lanthanum Halide crystals, a light guide, and a plurality of photomultiplier tubes arranged respectively peripherally around the cavity. The good timing resolution enables a time-of-flight (TOF) PET scanner to be developed that exhibits a reduction in noise propagation during image reconstruction and a gain in the signal-to-noise ratio. Such a PET scanner includes a time stamp circuit that records the time of receipt of gamma rays by respective PET detectors and provides timing data outputs that are provided to a processor that, in turn, calculates time-of-flight (TOF) of gamma rays through a patient in the cavity and uses the TOF of gamma rays in the reconstruction of images of the patient.

  15. Optimizing the lanthanum adsorption process onto chemically modified biomaterials using factorial and response surface design.

    PubMed

    Gabor, Andreea; Davidescu, Corneliu Mircea; Negrea, Adina; Ciopec, Mihaela; Grozav, Ion; Negrea, Petru; Duteanu, Narcis

    2017-01-29

    The rare metals' potential to pollute air, water, soil, and especially groundwater has received lot of attention recently. One of the most common rare earth group elements, lanthanum, is used in many industrial branches, and due to its toxicity, it needs to be eliminated from all residual aqueous solutions. The goal of this study was to evaluate the control of the adsorption process for lanthanum removal from aqueous solutions, using cellulose, a known biomaterial with high adsorbent properties, cheap, and environment friendly. The cellulose was chemically modified by functionalization with sodium β-glycerophosphate. The experimental results obtained after factorial design indicate optimum adsorption parameters as pH 6, contact time 60 min, and temperature 298 K, when the equilibrium concentration of lanthanum was 250 mg L(-1), and the experimental adsorption capacity obtained was 31.58 mg g(-1). Further refinement of the optimization of the adsorption process by response surface design indicates that at pH 6 and the initial concentration of 256 mg L(-1), the adsorption capacity has maximum values between 30.87 and 36.73 mg g(-1).

  16. Controlling the reaction between boron-containing sealing glass and a lanthanum-containing cathode by adding Nb2O5

    NASA Astrophysics Data System (ADS)

    Zhao, Dandan; Fang, Lihua; Tang, Dian; Zhang, Teng

    2016-09-01

    In solid oxide fuel cell (SOFC) stacks, the volatile boron species present in the sealing glass often react with the lanthanum-containing cathode, degrading the activity of the cathode (this phenomenon is known as boron poisoning). In this work, we report that this detrimental reaction can be effectively reduced by doping bismuth-containing borosilicate sealing glass-ceramic with a niobium dopant. The addition of Nb2O5 not only condenses the [SiO4] structural units in the glass network, but also promotes the conversion of [BO3] to [BO4]. Moreover, the Nb2O5 dopant enhances the formation of boron-containing phases (Ca3B2O6 and CaB2Si2O8), which significantly reduces the volatility of boron compounds in the sealing glass, suppressing the formation of LaBO3 in the reaction couple between the glass and the cathode. The reported results provide a new approach to solve the problem of boron poisoning.

  17. Optical, electrical and magnetic properties of lanthanum strontium manganite La1-xSrxMnO3 synthesized through the citrate combustion method.

    PubMed

    Turky, Ali Omar; Rashad, Mohamed Mohamed; Hassan, Ali Mostafa; Elnaggar, Elsayed M; Bechelany, Mikhael

    2017-03-01

    Generally, strontium-doped lanthanum manganites (LSM) are materials connected ordinarily as cathodes in the solid oxide fuel cell (SOFC). In this study, the structural, optical, electrical and magnetic properties of La1-xSrxMnO3 (x = 0.2, 0.5, 0.8) synthesized using an organic acid precursor strategy were investigated, based on using citric acid as a fuel. Evidently, the results disclosed that a pure single monoclinic LSM phase was obtained from the thermally treated precursors annealed at 1000 °C with an annealing time of 2 h. The microstructure of the formed sample relied on the Sr(2+) ion content. Moreover, a good optical transparency of 45-60% in a wide range of wavelengths between 800 and 1800 nm for all samples substituted by Sr(2+) ions was performed. The optical band gap energy was increased from 2.09 to 2.76 eV by increasing the Sr(2+) ion molar ratios. The trend in the calculated refractive index, the high frequency dielectric constant (εα) and the static dielectric constant (ε0) of all the produced samples can be linked to an increase in the Sr(2+) ion concentration. Moreover, the magnetic properties were enhanced with increasing Sr(2+) ion content.

  18. Development and validation of an ion chromatography method for the determination of phosphate-binding of lanthanum carbonate.

    PubMed

    Samy, Raghu; Faustino, Patrick J; Adams, Wallace; Yu, Lawrence; Khan, Mansoor A; Yang, Yongsheng

    2010-04-06

    Lanthanum carbonate is indicated to reduce serum phosphate in patients with end stage renal disease (ESRD). When given orally, lanthanum carbonate dissociates in the acid environment of the upper gastrointestinal tract to release lanthanum ions. The free lanthanum ions bind with dietary phosphate released from food during digestion to form highly insoluble lanthanum-phosphate complexes which prevent the absorption of phosphate, consequently reduce the serum phosphate. In order to evaluate the in vitro binding capacity of lanthanum carbonate, a simple and efficient ion chromatography (IC) method was developed and validated for determination of phosphate across the pH range encountered in the gastrointestinal tract. Chromatographic separation was achieved on a Dionex ICS-2000 IC system using a Dionex AS16, IonPac (4mmx250mm) analytical column and Dionex AG16, IonPac (4mmx50mm) guard column. Column temperature was maintained at 30 degrees C. Injection volume was 10microL. The compounds were eluted isocratically at a flow rate of 1mL/min and detected by suppressed conductivity. The analytical method was validated according to USP Category I requirements. The validation characteristics included accuracy, precision, quantification limit, linearity, and stability. The intra-day accuracy ranged from 89% to 103% for the solutions of pH 1.2-6.8. The intra-day precision (RSD) ranged from 0.6% to 3.7% for the solutions of pH 1.2-6.8. The analytical range was linear from 2 to 200ppm (mg/L). The R(2) ranged from 0.9998 to 1.0. This method was found to be simple, robust, sensitive, specific, and accurate. It has been successfully applied for determination of phosphate binding to lanthanum carbonate over the human gastrointestinal pH range at different time-points (from 0.5 to 24h).

  19. Long-term treatment with lanthanum carbonate reduces mineral and bone abnormalities in rats with chronic renal failure

    PubMed Central

    Damment, Stephen; Secker, Roger; Shen, Victor; Lorenzo, Victor; Rodriguez, Mariano

    2011-01-01

    Background. Lanthanum carbonate (FOSRENOL®, Shire Pharmaceuticals) is an effective non-calcium, non-resin phosphate binder for the treatment of hyperphosphataemia in patients with chronic kidney disease (CKD). In this study, we used a rat model of chronic renal failure (CRF) to examine the long-term effects of controlling serum phosphorus with lanthanum carbonate treatment on the biochemical and bone abnormalities associated with CKD–mineral and bone disorder (CKD–MBD). Methods. Rats were fed a normal diet (normal renal function, NRF), or a diet containing 0.75% adenine for 3 weeks to induce CRF. NRF rats continued to receive normal diet plus vehicle or normal diet supplemented with 2% (w/w) lanthanum carbonate for 22 weeks. CRF rats received a diet containing 0.1% adenine, with or without 2% (w/w) lanthanum carbonate. Blood and urine biochemistry were assessed, and bone histomorphometry was performed at study completion. Results. Treatment with 0.75% adenine induced severe CRF, as demonstrated by elevated serum creatinine. Hyperphosphataemia, hypocalcaemia, elevated calcium × phosphorus product and secondary hyperparathyroidism were evident in CRF + vehicle animals. Treatment with lanthanum carbonate reduced hyperphosphataemia and secondary hyperparathyroidism in CRF animals (P < 0.05), and had little effect in NRF animals. Bone histomorphometry revealed a severe form of bone disease with fibrosis in CRF + vehicle animals; lanthanum carbonate treatment reduced the severity of the bone abnormalities observed, particularly woven bone formation and fibrosis. Conclusions. Long-term treatment with lanthanum carbonate reduced the biochemical and bone abnormalities of CKD–MBD in a rat model of CRF. PMID:21098011

  20. Chromium remediation or release? Effect of iron(II) sulfate addition on chromium(VI) leaching from columns of chromite ore processing residue.

    PubMed

    Geelhoed, Jeanine S; Meeussen, Johannes C L; Roe, Martin J; Hillier, Stephen; Thomas, Rhodri P; Farmer, John G; Paterson, Edward

    2003-07-15

    Chromite ore processing residue (COPR), derived from the so-called high lime processing of chromite ore, contains high levels of Cr(III) and Cr(VI) and has a pH between 11 and 12. Ferrous sulfate, which is used for remediation of Cr(VI) contamination in wastewater and soils via reduction to Cr(III) and subsequent precipitation of iron(III)/chromium(III) hydroxide, has also been proposed for remediation of Cr(VI) in COPR. Instead, however, addition of FeSO4 to the infiltrating solution in column experiments with COPR greatly increased leaching of Cr(VI). Leached Cr(VI) increased from 3.8 to 12.3 mmol kg(-1) COPR in 25 pore volumes with 20 mM FeSO4, reaching solution concentrations as high as 1.6 mM. Fe(II) was ineffective in reducing Cr(VI) to Cr(III) because it precipitated when it entered the column due to the high pH of COPR, while Cr(VI) in solution was transported away with the infiltrating solution. The large increase in leaching of Cr(VI) upon infiltration of sulfate, either as FeSO4 or Na2SO4, was caused by anion exchange of sulfate for chromate in the layered double hydroxide mineral hydrocalumite, a process for which scanning electron microscopy with energy-dispersive X-ray microanalysis provided direct evidence.

  1. Effect of Organic Manures on the Growth of Cymbopogon citratus and Chrysopogon zizanioides for the Phytoremediation of Chromite-Asbestos Mine Waste: A Pot Scale Experiment.

    PubMed

    Kumar, Adarsh; Maiti, Subodh Kumar

    2015-01-01

    The abandoned chromite-asbestos mines are located in the Roro hills, West Singhbhum, Jharkhand, India, where mining operation ceased in 1983, and since then these mines are causing environmental pollution. The present study was planned to phytoremediate these metalloid and metal contaminated mine waste by using two aromatic grasses, Cymbopogon citratus and Chrysopogon zizanioides by applying different proportions of amendments (chicken manure, farmyard manure and garden soil). Mine waste has neutral pH, low electrical conductivity and organic carbon with higher concentration of total metals (Cr and Ni) as compared to soil. Application of manures resulted significant improvements of mine waste characteristics and plant growth, reduction in the availability of total extractable toxic metals (Cr, Ni) and increase in Mn, Zn and Cu concentration in the substrate. The maximum growth and biomass production for C. citratus and C. zizanioides were found in T-IV combination comprising of mine waste (90%), chicken manure (2.5%), farmyard manure (2.5%) and garden soil (5%). Addition of T-IV combination also resulted in low Cr and Ni accumulation in roots and reduction in translocation to shoots. Study indicates that C. citratus and C. zizanioides can be used for phytostabilization of abandoned chromite-asbestos mine waste with amendments.

  2. Origins of chromite and magnetite in sedimentary rocks deposited in a shallow water environment in the 3.2 Ga Moodies Group, South Africa

    NASA Astrophysics Data System (ADS)

    Otake, T.; Sakamoto, Y.; Itoh, S.; Yurimoto, H.; Kakegawa, T.

    2012-12-01

    *Otake, T. totake@eng.hokudai.ac.jp Div. of Sustainable Resources Engineering, Hokkaido Univ., Sapporo, Japan Sakamoto, Y. yu.sakamoto12@gmail.com Dep. of Earth Science, Tohoku Univ., Sendai, Japan Itoh, S. sitoh@ep.sci.hokudai.ac.jp Dep. of Natural History Sciences, Hokkaido Univ., Sapporo, Japan Yurimoto. H. yuri@ep.sci.hokudai.ac.jp Dep. of Natural History Sciences, Hokkaido Univ., Sapporo, Japan Kakegawa, T. kakegawa@m.tohoku.ac.jp Dep. of Earth Science, Tohoku Univ., Sendai, Japan Geochemical data from ferruginous chemical sedimentary rocks (e.g., Banded Iron Formation: BIF) have been used to reconstruct the surface environments of early Earth. However, only a few studies have investigated the geochemical characteristics of BIFs deposited in a shallow water environment during the Archean, which may have differed from those deposited in a deep water environment. Therefore, we investigated geological, petrographic and geochemical characteristics of ferruginous rocks deposited in a shallow water environment in the Moodies group, in the Barberton Greenstone Belt, South Africa. We obtained ferruginous rock samples in the Moodies group from both an outcrop and underground gold mine, and compared the characteristics of these samples. The 70 sedimentary rock samples were divided into groups based on the dominant Fe minerals they contain: Hematite-rich jaspilite (HM group), Magnetite-rich iron formation/shale/sandstone (MT group), and Siderite-rich sandstone (SD group). Samples in the HM group are predominantly composed of fine-grained quartz (< 20 μm) and hematite (< 5 μm), which are interpreted to be chemical precipitates. Samples in the MT group contain quartz, magnetite, siderite, ankerite, chlorite, biotite and chromite. The grain size of magnetite is much larger (20-150 μm) than that of hematite in the HM group. The magnetite is interpreted as a secondary mineral transformed from hematite during early diagenesis. Results of in situ oxygen isotope analysis by

  3. Chromium speciation and fractionation in ground and surface waters in the vicinity of chromite ore processing residue disposal sites.

    PubMed

    Farmer, John G; Thomas, Rhodri P; Graham, Margaret C; Geelhoed, Jeanine S; Lumsdon, David G; Paterson, Edward

    2002-04-01

    Chromium concentrations of up to 91 mg l(-1) were found by ICP-OES for ground water from nine boreholes at four landfill sites in an area of S.E. Glasgow/S. Lanarkshire where high-lime chromite ore processing residue (COPR) from a local chemical works had been deposited from 1830 to 1968. Surface water concentrations of up to 6.7 mg l(-1) in a local tributary stream fell to 0.11 mg l(-1) in the River Clyde. Two independent techniques of complexation/colorimetry and speciated isotope dilution mass spectrometry (SIDMS) showed that Cr was predominantly (>90%) in hexavalent form (CrVI) as CrO4(2-), as anticipated at the high pH (7.5-12.5) of the sites. Some differences between the implied and directly determined concentrations of dissolved CrIII, however, appeared related to the total organic carbon (TOC) content. This was most significant for the ground water from one borehole that had the highest TOC concentration of 300 mg l(-1) and at which < 3% of Cr was in the form of CrVI. Subsequent ultrafiltration produced significant decreases in Cr concentration with decreasing size fractions, e.g. <0.45 microm, < 100 kDa, <30 kDa and < 1 kDa by the tangential-flow method. As this appeared related more to concentrations of humic substances than of TOC per se, horizontal bed gel electrophoresis of freeze-dried ultrafilter retentates was carried out to further characterise the CrIII-organic complex. This showed for the main Cr-containing fraction, 100 kDa-0.45 microm, that the Cr was associated with a dark brown band characteristic of organic (humic) matter. Comparison of gel electrophoresis and FTIR results for ultrafilter retentates of ground water from this borehole with those for a borehole at another site where CrVI predominated suggested the influence of carboxylate groups, both in reducing CrVI and in forming soluble CrIII-humic complexes. The implications of this for remediation strategies (especially those based on the addition of organic matter) designed to reduce

  4. Lanthanum Nitrate As Electrolyte Additive To Stabilize the Surface Morphology of Lithium Anode for Lithium-Sulfur Battery.

    PubMed

    Liu, Sheng; Li, Guo-Ran; Gao, Xue-Ping

    2016-03-01

    Lithium-sulfur (Li-S) battery is regarded as one of the most promising candidates beyond conventional lithium ion batteries. However, the instability of the metallic lithium anode during lithium electrochemical dissolution/deposition is still a major barrier for the practical application of Li-S battery. In this work, lanthanum nitrate, as electrolyte additive, is introduced into Li-S battery to stabilize the surface of lithium anode. By introducing lanthanum nitrate into electrolyte, a composite passivation film of lanthanum/lithium sulfides can be formed on metallic lithium anode, which is beneficial to decrease the reducibility of metallic lithium and slow down the electrochemical dissolution/deposition reaction on lithium anode for stabilizing the surface morphology of metallic Li anode in lithium-sulfur battery. Meanwhile, the cycle stability of the fabricated Li-S cell is improved by introducing lanthanum nitrate into electrolyte. Apparently, lanthanum nitrate is an effective additive for the protection of lithium anode and the cycling stability of Li-S battery.

  5. Structural and magnetic properties of pure and Ca-doped LaCoO3 nanopowders obtained by a sol-gel route.

    PubMed

    Armelao, Lidia; Barreca, Davide; Bottaro, Gregorio; Maragno, Cinzia; Tondello, Eugenio; Caneschi, Andrea; Sangregorio, Claudio; Gialanella, Stefano

    2006-04-01

    Pure and Ca-doped LaCoO3 nanopowders were prepared by a non-alkoxidic sol-gel route using cobalt(II) acetate, lanthanum(III) nitrate and calcium(II) acetate as oxide precursors. The structural evolution and magnetic properties of the samples were studied as a function of thermal treatments in air up to 1273 K. In particular, the microstructure and composition of the systems were analyzed by X-ray Diffraction (XRD), Transmission Electron Microscopy (TEM), and X-ray Photoelectron Spectroscopy (XPS). Both pure and calcium-doped samples annealing at 973 K resulted in the formation of cubic LaCoO3 (average crystallite size <30 nm). This phase was fully retained in the calcium-doped materials even after annealing at higher temperatures, whereas a transition to the rhomboedral polymorph was detected in the pure samples at 1073 K. The magnetic behavior of the nanopowders was investigated as a function of temperature and applied field using both dynamic and static susceptibility measurements. Pure lanthanum cobaltite samples underwent a transition to an ordered state at 88 K, and their magnetic properties changed as a function of thermal treatments. As concerns calcium-doped samples, they ordered ferromagnetically at 171 and 185 K depending on the annealing temperature and displayed open hysteresis loops with coercive fields as large as 1.75 T at low temperatures.

  6. Optical Characteristics of La-Doped ZnS Thin Films Prepared by Chemical Bath Deposition

    NASA Astrophysics Data System (ADS)

    Xie, Hai-Qing; Chen, Yuan; Huang, Wei-Qing; Huang, Gui-Fang; Peng, Ping; Peng, Li; Wang, Tai-Hong; Zeng, Yun

    2011-02-01

    Undoped and La-doped ZnS thin films are prepared by chemical bath deposition (CBD) process through the co-precipitation reaction of inorganic precursors zinc sulfate, thiosulfate ammonia and La2O3. Composition of the films is analyzed using an energy-dispersive x-ray spectroscopy (EDS). Absorption spectra and spectral transmittances of the films are measured using a double beam UV-VIS spectrophotometer (TU-1901). It is found that significant red shifts in absorption spectra and decrease in absorptivity are obtained with increasing lanthanum. Moreover, optical transmittance is increased as La is doped, with a transmittance of more than 80% for wavelength above 360 nm in La-doped ZnS thin films. Compared to pure ZnS, the band gap decreases and flat-band potential positively shifts to quasi-metal for the La-doped ZnS. These results indicate that La-doped ZnS thin films could be valuably adopted as transparent electrodes.

  7. Enhancing the stability of copper chromite catalysts for the selective hydrogenation of furfural with ALD overcoating (II) – Comparison between TiO2 and Al2O3 overcoatings

    SciTech Connect

    Zhang, Hongbo; Canlas, Christian; Kropf, A. Jeremy; Elam, Jeffrey W.; Dumesic, James A; Marshall, Christopher L.

    2015-01-01

    TiO2 atomic layer deposition (ALD) overcoatings were applied to copper chromite catalysts to increase the stability for 2-furfuraldehyde (“furfural”) hydrogenation. After overcoating, about 75% activity was preserved compared to neat copper chromite: much higher activity than an alumina ALD overcoated catalyst with a similar number of ALD cycles. The effects of ALD TiO2 on the active Cu nanoparticles were studied extensively using both in-situ TPR/isothermal-oxidation and in-situ furfural hydrogenation via Cu XAFS. The redox properties of Cu were modified only slightly by the TiO2 ALD overcoat. However, a subtle electronic interaction was observed between the TiO2 ALD layers and the Cu nanoparticles. With calcination at 500 °C the interaction between the TiO2 overcoat and the underlying catalyst is strong enough to inhibit migration and site blocking by chromite, but is sufficiently weaker than the interaction between the Al2O3 overcoat and copper chromite that it does not strongly inhibit the catalytic activity of the copper nanoparticles.

  8. Studies on Synthesis, Structural and Electrical Properties of Complex Oxide Thin Films: Barium Strontium Titanate and Lanthanum Strontium Nickelate

    NASA Astrophysics Data System (ADS)

    Podpirka, Adrian A.

    High performance miniaturized passives are of great importance for advanced nanoelectronic packages for several applications including efficient power delivery. Low cost thin film capacitors fabricated directly on package (and/or on-chip) are an attractive approach towards realizing such devices. This thesis aims to explore fundamental frequency dependent dielectric and insulating properties of thin film high-k dielectric constant in the perovskite and perovskite-related complex oxides. Throughout this thesis, we have successfully observed the role of structure, strain and oxygen stoichiometry on the dielectric properties of thin film complex oxides, allowing a greater understanding of processing conditions and polarization mechanisms. In the first section of the thesis, we explore novel processing methods in the conventional ferroelectric, barium strontium titanate, Ba1-xSr xTiO3 (BST), using ultraviolet enhanced oxidation techniques in order to achieve improvements in the dielectric properties. Using this method, we also explore the growth of BST on inexpensive non-noble metals such as Ni which presents technical challenges due to the ability to oxidize at high temperatures. We observe a significant lowering of the dielectric loss while also lowering the process temperature which allows us to maintain an intimate interface between the dielectric layer and the metal electrode. The second section of this thesis explores the novel dielectric material, Lanthanum Strontium Nickelate, La2-xSrxNiO4 (LSNO), which exhibits a colossal dielectric response. For the first time, we report on the colossal dielectric properties of polycrystalline and epitaxial thin film LSNO. We observe a significant polarization dependence on the microstructure due to the grain/grain boundary interaction with charged carriers. We next grew epitaxial films on various insulating oxide substrates in order to decouple the grain boundary interaction. Here we observed substrate dependent dielectric

  9. Nonaqueous synthesis of metal oxide nanoparticles: Short review and doped titanium dioxide as case study for the preparation of transition metal-doped oxide nanoparticles

    SciTech Connect

    Djerdj, Igor Arcon, Denis; Jaglicic, Zvonko; Niederberger, Markus

    2008-07-15

    The liquid-phase synthesis of metal oxide nanoparticles in organic solvents under exclusion of water is nowadays a well-established alternative to aqueous sol-gel chemistry. In this article, we highlight some of the advantages of these routes based on selected examples. The first part reviews some recent developments in the synthesis of ternary metal oxide nanoparticles by surfactant-free nonaqueous sol-gel routes, followed by the discussion of the morphology-controlled synthesis of lanthanum hydroxide nanoparticles, and the presentation of structural peculiarities of manganese oxide nanoparticles with an ordered Mn vacancy superstructure. These examples show that nonaqueous systems, on the one hand, allow the preparation of compositionally complex oxides, and, on the other hand, make use of the organic components (initially present or formed in situ) in the reaction mixture to tailor the morphology. Furthermore, obviously even the crystal structure can differ from the corresponding bulk material like in the case of MnO nanoparticles. In the second part of the paper we present original results regarding the synthesis of dilute magnetic semiconductor TiO{sub 2} nanoparticles doped with cobalt and iron. The structural characterization as well as the magnetic properties with special attention to the doping efficiency is discussed. - Graphical abstract: In the first part of this article, nonaqueous sol-gel routes to ternary metal oxide nanoparticles are briefly reviewed, followed by the discussion of the morphology-controlled synthesis of lanthanum hydroxide nanoparticles, and the appearance of an unprecedented superstructure in MnO nanoparticles. In the second part, doping experiments of TiO{sub 2} with Fe and Co are presented, along with their characterization including magnetic measurements.

  10. Comparison of the local and the average crystal structure of proton conducting lanthanum tungstate and the influence of molybdenum substitution.

    PubMed

    Magrasó, Anna; Frontera, Carlos

    2016-03-07

    We report on the comparison of the local and average structure reported recently for proton conducting lanthanum tungstate, of general formula La28-xW4+xO54+δv2-δ, and the impact of molybdenum-substitution on the crystal structure of the material. Partial replacement of W with 10 and 30 mol% Mo is investigated here, i.e. La27(W1-xMox)5O55.5 for x = 0.1 and 0.3. This study addresses the interpretation and the description of a disordered cation and anion sublattice in this material, which enables the understanding of the fundamental properties related to hydration, transport properties and degradation in lanthanum tungstate. The report shows that Mo-substituted lanthanum tungstate is a promising material as a dense oxide membrane for hydrogen separation at intermediate temperatures.

  11. The effect of lanthanum on the nexus of the anterior byssus retractor muscle of Mytilus edulis L.

    PubMed

    Brink, P R; Kensler, R W; Dewey, M M

    1979-01-01

    The nexus of the anterior byssus retractor muscle (ABRM) of Mytilus has been observed with freeze-fracture techniques. Pits appear in the EF face and particles in the PF face, designating it as an A-type nexus. Under control conditions (lanthanum-free) the center-to-center spacing of pits and particles ranged from 14.0 nm to 15.5 nm. When lanthanum chloride (5 mM) was used in incubation media before fixation and glycerination, marked changes in the nexal membrane were observed. These changes involved close packing and long-range ordering of pits in the EF face, as shown by optical diffraction. In the presence of lanthanum the center-to-center spacing of the pits was 11.7 nm, while the particles remained at a spacing of 15.0 nm. From this we conclude that specific agents can alter the array of pits and particles in a nexus (gap junction).

  12. Removal of arsenic(III) and arsenic(IV) ions from aqueous solutions with lanthanum(III) salt and comparison with aluminum(III), calcium(II), and iron(III) salts

    SciTech Connect

    Tokunaga, S.; Yokoyama, S.; Wasay, S.A.

    1999-05-01

    Interactions of arsenic(III) and arsenic(V) ions with a lanthanum salt were studied with the aim of developing a new precipitation method for removal of arsenic from aqueous solutions. Performance was compared to those of aluminum, polyaluminum chloride (PAC), calcium, and iron(III) salts. Arsenic(III) was removed by iron(III) and lanthanum in a narrow pH range with less than 605 removal. Arsenic(V) was removed more efficiently by aluminum, PAC, iron(III), and lanthanum. Lanthanum was most effective, meeting Japanese effluent and drinking water standards by adding three times as much lanthanum as arsenic(V).

  13. Rutherford backscattering spectrometry (RBS) characterization of oxide scale formed on (AISI-304) steel after surface deposition of lanthanum

    SciTech Connect

    Ager, F.J.; Respaldiza, M.A.; Benitez, J.J.; Odriozola, J.A.; Botella, J.; Soares, J.C.; Silva, M.F. da

    1996-02-01

    Oxidized AISI-304 steel samples coated with lanthanum have been investigated by Rutherford backscattering spectrometry (RBS) in order to determine the composition profile of the oxide scale. In this sense, RBS technique has been revealed as a very reliable and nondestructive method for depth profile analysis. Lanthanum deposition, specially over preoxidized specimens, has proven to improve their resistance to high temperature oxidation. The formation of a LaCrO{sub 3} perovskite-like phase uniformly distributed along the oxide scale is proposed as being responsible for this behavior.

  14. Thermochemistry of perovskites in the lanthanum-strontium-manganese-iron oxide system

    NASA Astrophysics Data System (ADS)

    Marinescu, Cornelia; Vradman, Leonid; Tanasescu, Speranta; Navrotsky, Alexandra

    2015-10-01

    The enthalpies of formation from binary oxides of perovskites (ABO3) based on lanthanum strontium manganite La(Sr)MnO3 (LSM) and lanthanum strontium ferrite La(Sr)FeO3 (LSF) and mixed lanthanum strontium manganite ferrite La(Sr)Mn(Fe)O3 (LSMF) were measured by high temperature oxide melt solution calorimetry. Using iodometric titration, the oxygen content was derived. The perovskites with A-site cation deficiency have greater oxygen deficiency than the corresponding A-site stoichiometric series. Stability of LSMF decreases with increasing iron content. Increasing oxygen deficiency clearly destabilizes the perovskites. The results suggest an enthalpy of oxygen incorporation that is approximately independent of composition. 0.35La2O3 (xl, 25 °C)+Mn2O3 (xl, 25 °C)+0.3SrO (xl, 25 °C)+Fe2O3 (xl, 25 °C)+O2 (g, 25 °C)→La0.7Sr0.3Mn1-yFeyO3-δ (xl, 25 °C). (b) ∆ Hf,ox* (La0.7Sr0.3Mn1-yFeyO3-δ) .0.35 La2O3 (xl, 25 ººC) + (0.7-y+ 2δ)/2 Mn2O3 (xl, 25 ºC) + 0.3 SrO (xl, 25 ºC) + y/2Fe2O3 (xl, 25 ºC) + (0.3-2δ) MnO2 (xl, 25 ºC)→La0.7Sr0.3Mn1-yFeyO3-δ (xl, 25 ºC).

  15. Lanthanum-catalysed synthesis of microporous 3D graphene-like carbons in a zeolite template

    NASA Astrophysics Data System (ADS)

    Kim, Kyoungsoo; Lee, Taekyoung; Kwon, Yonghyun; Seo, Yongbeom; Song, Jongchan; Park, Jung Ki; Lee, Hyunsoo; Park, Jeong Young; Ihee, Hyotcherl; Cho, Sung June; Ryoo, Ryong

    2016-07-01

    Three-dimensional graphene architectures with periodic nanopores—reminiscent of zeolite frameworks—are of topical interest because of the possibility of combining the characteristics of graphene with a three-dimensional porous structure. Lately, the synthesis of such carbons has been approached by using zeolites as templates and small hydrocarbon molecules that can enter the narrow pore apertures. However, pyrolytic carbonization of the hydrocarbons (a necessary step in generating pure carbon) requires high temperatures and results in non-selective carbon deposition outside the pores. Here, we demonstrate that lanthanum ions embedded in zeolite pores can lower the temperature required for the carbonization of ethylene or acetylene. In this way, a graphene-like carbon structure can be selectively formed inside the zeolite template, without carbon being deposited at the external surfaces. X-ray diffraction data from zeolite single crystals after carbonization indicate that electron densities corresponding to carbon atoms are generated along the walls of the zeolite pores. After the zeolite template is removed, the carbon framework exhibits an electrical conductivity that is two orders of magnitude higher than that of amorphous mesoporous carbon. Lanthanum catalysis allows a carbon framework to form in zeolite pores with diameters of less than 1 nanometre; as such, microporous carbon nanostructures can be reproduced with various topologies corresponding to different zeolite pore sizes and shapes. We demonstrate carbon synthesis for large-pore zeolites (FAU, EMT and beta), a one-dimensional medium-pore zeolite (LTL), and even small-pore zeolites (MFI and LTA). The catalytic effect is a common feature of lanthanum, yttrium and calcium, which are all carbide-forming metal elements. We also show that the synthesis can be readily scaled up, which will be important for practical applications such as the production of lithium-ion batteries and zeolite-like catalyst

  16. High-current lanthanum-hexaboride electron emitter for a quasi-stationary arc plasma generator

    SciTech Connect

    Davydenko, V. I. Ivanov, A. A. Shul’zhenko, G. I.

    2015-11-15

    A high-current electron emitter on the basis of lanthanum hexaboride is developed for quasi-stationary arc plasma generators of ion sources. The emitter consists of a set of LaB{sub 6} washers interleaved with washers made of thermally extended graphite. The emitter is heated by the current flowing through the graphite washers. The thermal regime of emitter operation during plasma generation is considered. The emitter has been successfully used in the ion sources of the diagnostic injectors of fast hydrogen atomic beams.

  17. Fabrication of Lanthanum Telluride 14-1-11 Zintl High-Temperature Thermoelectric Couple

    NASA Technical Reports Server (NTRS)

    Ravi, Vilupanur A.; Li, Billy Chun-Yip; Fleurial, Pierre; Star, Kurt

    2010-01-01

    The development of more efficient thermoelectric couple technology capable of operating with high-grade heat sources up to 1,275 K is key to improving the performance of radioisotope thermoelectric generators. Lanthanum telluride La3-xTe4 and 14-1-11 Zintls (Yb14MnSb11) have been identified as very promising materials. The fabrication of advanced high-temperature thermoelectric couples requires the joining of several dissimilar materials, typically including a number of diffusion bonding and brazing steps, to achieve a device capable of operating at elevated temperatures across a large temperature differential (up to 900 K). A thermoelectric couple typically comprises a heat collector/ exchanger, metallic interconnects on both hot and cold sides, n-type and ptype conductivity thermoelectric elements, and cold-side hardware to connect to the cold-side heat rejection and provide electrical connections. Differences in the physical, mechanical, and chemical properties of the materials that make up the thermoelectric couple, especially differences in the coefficients of thermal expansion (CTE), result in undesirable interfacial stresses that can lead to mechanical failure of the device. The problem is further complicated by the fact that the thermoelectric materials under consideration have large CTE values, are brittle, and cracks can propagate through them with minimal resistance. The inherent challenge of bonding brittle, high-thermal-expansion thermoelectric materials to a hot shoe material that is thick enough to carry the requisite electrical current was overcome. A critical advantage over prior art is that this device was constructed using all diffusion bonds and a minimum number of assembly steps. The fabrication process and the materials used are described in the following steps: (1) Applying a thin refractory metal foil to both sides of lanthanum telluride. To fabricate the n-type leg of the advanced thermoelectric couple, the pre-synthesized lanthanum

  18. Deposition of Lanthanum Strontium Cobalt Ferrite (LSCF) Using Suspension Plasma Spraying for Oxygen Transport Membrane Applications

    NASA Astrophysics Data System (ADS)

    Fan, E. S. C.; Kesler, O.

    2015-08-01

    Suspension plasma spray deposition was utilized to fabricate dense lanthanum strontium cobalt ferrite oxygen separation membranes (OSMs) on porous metal substrates for mechanical support. The as-sprayed membranes had negligible and/or reversible material decomposition. At the longer stand-off distance (80 mm), smooth and dense membranes could be manufactured using a plasma with power below approximately 81 kW. Moreover, a membrane of 55 μm was observed to have very low gas leakage rates desirable for OSM applications. This thickness could potentially be decreased further to improve oxygen diffusion by using metal substrates with finer surface pores.

  19. Temperature-Dependent Electrical and Micromechanical Properties of Lanthanum Titanate with Additions of Yttria

    NASA Technical Reports Server (NTRS)

    Goldsby, Jon C.

    2010-01-01

    Temperature-dependent elastic properties were determined by establishing continuous flexural vibrations in the material at its lowest resonance frequency of 31tHz. The imaginary part of the complex impedance plotted as a function of frequency and temperature reveals a thermally activated peak, which decreases in magnitude as the temperature increases. Additions of yttria do not degrade the electromechanical in particularly the elastic and anelastic properties of lanthanum titanate. Y2O3/La2Ti2O7 exhibits extremely low internal friction and hence may be more mechanical fatigue-resistant at low strains.

  20. Grain Boundary Engineering of Lithium-Ion-Conducting Lithium Lanthanum Titanate for Lithium-Air Batteries

    DTIC Science & Technology

    2015-01-01

    Tojo T, Sakurai Y. Synthesis and lithium - ion conductivity for perovskite-type Li3/8Sr7/16Ta3/4Zr1/4O3 solid electrolyte by powder-bed sintering...battery performance is limited by the electrolytic membrane, which needs high Li-ionic conductivity. Lithium lanthanum titanate (Li3xLa(2/3)-xTiO3, or...of the A-site ions and lithium ion conductivity in the perovskite solid solution La0.67-xLi3xTiO3 (x=0.11). Journal of Solid State Ionics. 1999;121

  1. Advances in the Low Temperature Preparation and Structural Characterization of Lanthanum Strontium Manganite Powder

    DTIC Science & Technology

    2001-04-01

    with divalent Sr 2+ cations [16,17]. U3.3.1 The aim of this work is to synthesize , by "chimie douce" technique, lanthanum strontium manganite powders...simple citrates in hot ammoniacal solution. The solution is then evaporated and grounded. TGA and TPR analyses show that the heating of citrates leads to...close to the x = 0.10 single crystal synthesized at 1200’C by A. Urushibara et al. [22] which is orthorhombic. A less oxidizing atmosphere during the

  2. Analysis of the elements sputtered during the lanthanum implantation in stainless steels

    NASA Astrophysics Data System (ADS)

    Ager, F. J.; Respaldiza, M. A.; Paúl, A.; Odriozola, J. A.; Lobato, J. M.; da Silva, M. F.; Redondo, L. M.; Soares, J. C.

    1998-04-01

    The evidence of the modification of the surface structure of the AISI-304 stainless steel during the implantation of lanthanum makes the analysis of the sputtered elements very interesting. Those sputtered elements are deposited on a carbon sheet placed in front of the steel being implanted, and studied by means of RBS and PIXE, together with the implanted specimens. Besides, the protective effect of the implanted ions during the high temperature oxidation is also studied by those techniques together with XRD and thermogravimetric methods.

  3. Temperature Dependent Electrical and Micromechanical Properties of Lanthanum Titanate with Additions of Yttria

    NASA Technical Reports Server (NTRS)

    Goldsby, Jon C.

    2003-01-01

    Lanthanum titanate (La2Ti2O7) a layered distorted perovskite (1) with space group Pna2(sub 1) has been shown to have potential as a high temperature piezoelectric (2). However this highly refractory oxide compound must be consolidated at relatively high temperatures approximately 1400 C. Commercial La2Ti207 powders were mechanically alloyed with additions of Y2O3 to lower the consolidation temperature by 300 C and to provide post processing mechanical stability. Temperature dependent electrical, elastic and anelastic behavior were selected as nondestructive means of evaluating the effects of yttria on the properties of this ferroceramic material.

  4. The influence of the Jahn-Teller effect at Fe2+ on the structure of chromite at high pressure

    NASA Astrophysics Data System (ADS)

    Kyono, Atsushi; Gramsch, Stephen A.; Yamanaka, Takamitsu; Ikuta, Daijo; Ahart, Muhtar; Mysen, Bjørn O.; Mao, Ho-Kwang; Hemley, Russell J.

    2012-02-01

    The crystal structure of chromite FeCr2O4 was investigated to 13.7 GPa and ambient temperature with single-crystal X-ray diffraction techniques. The unit-cell parameter decreases continuously from 8.3832 (5) to 8.2398 (11) Å up to 11.8 GPa. A fit to the Birch-Murnaghan equation of state (EoS) based on the P-V data gives: K 0 = 209 (13) GPa, K' = 4.0 (fixed), and V 0 = 588 (1) Å3. The FeO4 tetrahedra and CrO6 octahedra are compressed isotropically with pressure with their Fe-O and Cr-O bond distances decreasing from 1.996 (6) to 1.949 (7) Å and from 1.997 (3) to 1.969 (7) Å, respectively. The tetrahedral site occupied by the Fe2+ cation is more compressible than the octahedral site occupied by the Cr3+ cation. The resulting EoS parameters for the tetrahedral and the octahedral sites are K 0 = 147 (9) GPa, K' = 4.0 (fixed), V 0 = 4.07 (1) Å3 and K 0 = 275 (24) GPa, K' = 4.0 (fixed), V 0 = 10.42 (2) Å3, respectively. A discontinuous volume change is observed between 11.8 and 12.6 GPa. This change indicates a phase transition from a cubic (space group Fd-{overline{3}} m) to a tetragonal structure (space group I41 /amd). At the phase transition boundary, the two Cr-O bonds parallel to the c-axis shorten from 1.969 (7) to 1.922 (17) Å and the other four Cr-O bonds parallel to the ab plane elongate from 1.969 (7) to 1.987 (9) Å. This anisotropic deformation of the octahedra leads to tetragonal compression of the unit cell along the c-axis. The angular distortion in the octahedron decreases continuously up to 13.7 GPa, whereas the distortion in the tetrahedron rises dramatically after the phase transition. At the pressure of the phase transition, the tetrahedral bond angles along the c-axis direction of the unit cell begin decreasing from 109.5° to 106.6 (7)°, which generates a "stretched" tetrahedral geometry. It is proposed that the Jahn-Teller effect at the tetrahedrally coordinated Fe2+ cation becomes active with compression and gives rise to the tetrahedral

  5. Using human sweat to extract chromium from chromite ore processing residue: applications to setting health-based cleanup levels.

    PubMed

    Horowitz, S B; Finley, B L

    1993-12-01

    Chromite ore processing residue (COPR) containing measurable levels of hexavalent and trivalent chromium. [Cr(VI) and Cr(III), respectively] has been used to fill in low-lying areas in Hudson County, N.J. While it has been demonstrated that direct dermal contact with solutions containing Cr(VI) may elicit allergic contact dermatitis (ACD) in previously sensitized individuals, it is unknown to what degree skin moisture may solubilize Cr(VI) from COPR adhering to skin. An accurate estimate of this extraction potential is necessary to establish COPR concentrations of Cr(VI) and Cr(III) that are protective of eliciting ACD in sensitized individuals. The purpose of this study was to measure the extractable fraction of Cr(VI) and total chromium [Cr(III) and Cr(VI)] in soils impacted by COPR using human sweat as the extractant. Human sweat was collected from seven male volunteers. Samples of COPR material containing the following Cr(VI) and total chromium concentrations were collected: Cr(VI), 16, 136, and 1240 ppm; total chromium, 932 and 6660 ppm. The samples were sieved to obtain a uniform particle size < 500 microns. The samples were then mixed with human sweat at 30 degrees C for 12 h, after which the sweat was filtered and analyzed to determine the dissolved concentration of Cr(VI) and total chromium. The data from these analyses show that no detectable levels (limit of detection = 0.010 ppm) of Cr(VI) were leached from COPR containing 16 ppm Cr(VI). At Cr(VI) concentrations of 136 and 1240 ppm, less than 0.1% of the Cr(VI) present in the COPR sample was extracted into sweat, and sweat concentrations were 0.133 ppm Cr(VI) or less. Similarly, the amount of Crtotal extracted was 0.3% or less at COPR concentrations as high as 6600 ppm Crtotal, and sweat concentrations were 2.3 ppm Crtotal or less. If a minimum concentration of 10 ppm (Bagdon and Hazen, 1991) to 54 ppm (Paustenbach et al., 1992) Cr(VI) in sweat is required to elicit an ACD response in chromium

  6. Niobium doped lanthanum calcium ferrite perovskite as a novel electrode material for symmetrical solid oxide fuel cells

    NASA Astrophysics Data System (ADS)

    Kong, Xiaowei; Zhou, Xiaoliang; Tian, Yu; Wu, Xiaoyan; Zhang, Jun; Zuo, Wei

    2016-09-01

    Development of cost-effective and efficient electrochemical catalysts for the fuel cells electrode is of prime importance to emerging renewable energy technologies. Here, we report for the first time the novel La0.9Ca0.1Fe0.9Nb0.1O3-δ (LCFNb) perovskite with good potentiality for the electrode material of the symmetrical solid oxide fuel cells (SSOFC). The Sc0.2Zr0.8O2-δ (SSZ) electrolyte supported symmetrical cells with impregnated LCFNb and LCFNb/SDC (Ce0.8Sm0.2O2-δ) electrodes achieve relatively high power outputs with maximum power densities (MPDs) reaching up to 392 and 528.6 mW cm-2 at 850 °C in dry H2, respectively, indicating the excellent electro-catalytic activity of LCFNb towards both hydrogen oxidation and oxygen reduction. Besides, the MPDs of the symmetrical cells with LCFNb/SDC composite electrodes in CO and syngas (CO: H2 = 1:1) are almost identical to those in H2, implying that LCFNb material has similar catalytic activities to carbon monoxide compared with hydrogen. High durability in both H2, CO and syngas during the short term stability tests for 50 h are also obtained, showing desirable structure stability, and carbon deposition resistance of LCFNb based electrodes. The present results indicate that the LCFNb perovskite with remarkable cell performance is a promising electrode material for symmetrical SOFCs.

  7. Barium carbonate nanoparticle to enhance oxygen reduction activity of strontium doped lanthanum ferrite for solid oxide fuel cell

    NASA Astrophysics Data System (ADS)

    Hong, Tao; Chen, Fanglin; Xia, Changrong

    2015-03-01

    BaCO3 nanoparticles are demonstrated as outstanding catalysts for high-temperature oxygen reduction reaction (ORR) on the La0.8Sr0.2FeO3-δ (LSF) cathode for solid oxide fuel cells (SOFCs) based on ytrria-stabilized zirconia (YSZ) electrolytes. Thermal gravitational and X-ray diffraction measurements show that BaCO3 is stable and chemically compatible with LSF under the fabrication and operation conditions of intermediate-temperature SOFCs. The BaCO3 nanoparticles can greatly reduce the interfacial polarization resistance; from 2.96 to 0.84 Ω cm2 at 700 °C when 12.9wt% BaCO3 is infiltrated to the porous LSF electrode on the YSZ electrolyte. Electrochemical impedance spectroscopy shows that there is about one order of magnitude decrease in the low-frequency resistance, indicating that BaCO3 nanoparticles can greatly enhance the surface steps for ORR. Electrical conductivity relaxation investigation indicates about one order of magnitude increase in the chemical oxygen surface exchange coefficient when BaCO3 is applied, directly demonstrating significant increase in the kinetics for ORR. In addition, LSF cathodes with infiltrated BaCO3 nanoparticles have shown excellent stability and substantially enhanced cell performance as demonstrated with single cells, suggesting BaCO3 nanoparticles are very effective in enhancing ORR on LSF.

  8. Effect of thickness on microwave absorptive behavior of La-Na doped Co-Zr barium hexaferrites in 18.0-26.5 GHz band

    NASA Astrophysics Data System (ADS)

    Arora, Amit; Narang, Sukhleen Bindra; Pubby, Kunal

    2017-02-01

    In this research, the microwave properties of Lanthanum-Sodium doped Cobalt-Zirconium barium hexaferrites, intended as microwave absorbers, are analyzed on Vector Network Analyzer in K-band. The results indicate that the doping has resulted in lowering of real permittivity and enhancement of dielectric losses. Real permeability has shown increase while magnetic losses have shown decrease in value with doping. All these four properties have shown very small variation with frequency in the scanned frequency range which indicates the relaxation type of behavior. Microwave absorption characteristics of these compositions are analyzed with change in sample thickness. The results demonstrate that the matching frequency of the microwave absorber shifts towards lower side of frequency band with increase in thickness. The complete analysis of the prepared microwave absorbers shows a striking achievement with very low reflection loss and wide absorption bandwidth for all the six compositions in 18-26.5 GHz frequency band.

  9. A polynuclear coordination glutarate of lanthanum(III) with an uncommon cage feature.

    PubMed

    Benmerad, Belkacem; Guehria-Laïdoudi, Acoura; Dahaoui, Slimane; Lecomte, Claude

    2004-03-01

    The title compound, triaquatris(glutarato)dilanthanum(III) dihydrate, [[La2(C5H6O4)3(H2O)3] x 2H2O]n, is the first reported glutarate coordination polymer of lanthanum(III) without a protonated ligand. The noteworthy features in the structure are, firstly, the unusual binuclear lanthanum cage formed by three bridging bonds through O atoms involved in different coordination modes and, secondly, the very rare 'malonate' mode exhibited by a dicarboxylate ligand with an alkyl chain of five C atoms. To our knowledge, this eta7 chelation for the glutarate ligand has not been reported and was thought to be forbidden for steric reasons. The gauche-gauche conformation of the corresponding ligand favours cage formation, but trans geometries created along the ligating O atoms prevent cluster packing. The two independent La atoms are nine- and tenfold coordinated, leading to distorted one-face-sharing LaO7(H2O)2 and LaO9(H2O) polyhedra, respectively. In the three-dimensional framework, these asymmetric subunits are linked in a zigzag manner via one-edge-sharing LaO9(H2O) polyhedra and are connected by the carbon backbone chains of the ligands. The structure is very compact and, unlike many other reported dicarboxylate lanthanides, connectivity between the two metal atoms and the three ligands yields a crystal packing with cavities accommodating two guest water molecules but without an open framework.

  10. Cr(VI) Adsorption on Red Mud Modified by Lanthanum: Performance, Kinetics and Mechanisms.

    PubMed

    Cui, You-Wei; Li, Jie; Du, Zhao-Fu; Peng, Yong-Zhen

    Water pollution caused by the highly toxic metal hexavalent chromium (Cr(VI)) creates significant human health and ecological risks. In this study, a novel adsorbent was used to treat Cr(VI)-containing wastewater; the adsorbent was prepared using red mud (RM) generated from the alumina production industry and the rare earth element lanthanum. This study explored adsorption performance, kinetics, and mechanisms. Results showed that the adsorption kinetics of the RM modified by lanthanum (La-RM), followed the pseudo-second-order model, with a rapid adsorption rate. Cr(VI) adsorption was positively associated with the absorbent dose, pH, temperature, and initial Cr(VI) concentration; coexisting anions had little impact. The maximum Cr(VI) adsorption capacity was 17.35 mg/g. Cr(VI) adsorption on La-RM was a mono-layer adsorption pattern, following the Langmuir isotherm model. Thermodynamic parameters showed the adsorption was spontaneous and endothermic. The adsorption of Cr(VI) on La-RM occurred as a result of LaOCl formation on the RM surface, which in turn further reacted with Cr(VI) in the wastewater. This study highlighted a method for converting industrial waste into a valuable material for wastewater treatment. The novel absorbent could be used as a potential adsorbent for treating Cr(VI)-contaminating wastewater, due to its cost-effectiveness and high adsorption capability.

  11. Influence of dissolved organic carbon on the efficiency of P sequestration by a lanthanum modified clay.

    PubMed

    Dithmer, Line; Nielsen, Ulla Gro; Lundberg, Daniel; Reitzel, Kasper

    2016-06-15

    A laboratory scale experiment was set up to test the effect of dissolved organic carbon (DOC) as well as ageing of the La-P complex formed during phosphorus (P) sequestration by a La modified clay (Phoslock(®)). Short term (7 days) P adsorption studies revealed a significant negative effect of added DOC on the P sequestration of Phoslock(®), whereas a long-term P adsorption experiment revealed that the negative effect of added DOC was reduced with time. The reduced P binding efficiency is kinetic, as evident from solid-state (31)P magic-angle spinning (MAS) NMR spectroscopy, who showed that the P binding did not change in the presence of DOC. (31)P MAS NMR also reveals that up to 26% of the sequestered phosphate is as loosely bound redox-sensitive P species on the surface of rhabdophane (LaPO4 · nH2O, n ≤ 3). The ratio between the loosely bound P and lanthanum phosphate did not change with time, however both NMR and La LIII-extended x-ray absorption fine structure (EXAFS) spectroscopy shows a transformation of lanthanum phosphate from the initially formed rhabdophane towards the more stable monazite (LaPO4). Furthermore, the effect of natural DOC on the P binding capacity was tested using water and pore water from 16 Danish lakes. Whilst DOC has an immediate negative impact on P binding in the lake water, with time this effect is reduced.

  12. Cr(VI) Adsorption on Red Mud Modified by Lanthanum: Performance, Kinetics and Mechanisms

    PubMed Central

    Cui, You-Wei; Li, Jie; Du, Zhao-Fu; Peng, Yong-Zhen

    2016-01-01

    Water pollution caused by the highly toxic metal hexavalent chromium (Cr(VI)) creates significant human health and ecological risks. In this study, a novel adsorbent was used to treat Cr(VI)-containing wastewater; the adsorbent was prepared using red mud (RM) generated from the alumina production industry and the rare earth element lanthanum. This study explored adsorption performance, kinetics, and mechanisms. Results showed that the adsorption kinetics of the RM modified by lanthanum (La-RM), followed the pseudo-second-order model, with a rapid adsorption rate. Cr(VI) adsorption was positively associated with the absorbent dose, pH, temperature, and initial Cr(VI) concentration; coexisting anions had little impact. The maximum Cr(VI) adsorption capacity was 17.35 mg/g. Cr(VI) adsorption on La-RM was a mono-layer adsorption pattern, following the Langmuir isotherm model. Thermodynamic parameters showed the adsorption was spontaneous and endothermic. The adsorption of Cr(VI) on La-RM occurred as a result of LaOCl formation on the RM surface, which in turn further reacted with Cr(VI) in the wastewater. This study highlighted a method for converting industrial waste into a valuable material for wastewater treatment. The novel absorbent could be used as a potential adsorbent for treating Cr(VI)-contaminating wastewater, due to its cost-effectiveness and high adsorption capability. PMID:27658113

  13. Pre-existing oral contrast from lanthanum carbonate: a confounding factor in CT mesenteric angiography.

    PubMed

    Bull, M D; Shrimanker, R; Thomas, M R M; Mulgrew, C J

    2012-04-01

    A 69-year-old male was referred from the renal unit to radiology for investigation of bleeding per rectum. A CT mesenteric angiogram was performed. However, it was noted on the pre-contrast images that the large bowel contained positive oral contrast media. The procedure was abandoned as it would have been difficult to see extravasation of intravenous contrast from a bleeding point in the large bowel. The initial belief was that either the patient had been given oral contrast by ward staff on the assumption that it would be needed, or had had a recent radiological study requiring contrast, which was still present. Neither was the case; it emerged that the patient was taking Fosrenol (Shire Pharmaceuticals, Wayne, PA), a lanthanum carbonate medication used in the treatment of hyperphosphataemia. Lanthanum is densely radio-opaque and appears as positive bowel contrast on CT and plain radiography studies. When considering radiological studies specifically requiring the absence of oral contrast, it is important to be aware of the patient's drug history to avoid non-diagnostic scans with the associated radiation exposure.

  14. Three-year follow-up of lanthanum carbonate therapy in hemodialysis patients.

    PubMed

    Takeuchi, Kazuhisa; Matsuda, Etsuko; Sekino, Makoto; Hasegawa, Yukiko; Kamo, Yoshie; Kikuchi, Natsue; Sekino, Hiroshi

    2013-04-01

    For 3 years following the start of lanthanum carbonate therapy, effects on other pharmaceutical treatment with sevelamer hydrochloride (SH), calcium carbonate (CC), and vitamin D, and those on clinical condition were examined. Dialysis patients with hyperphosphatemia (89 cases; average age 55.2 years; dialysis history of 10 years; 50 male and 39 female), who agreed to start lanthanum carbonate (LC) administration, were observed for a mean period of 32.6 ± 6.2 months. Mean daily dosages of CC and SH before starting LC were 2.68 g and 0.73 g; mean daily dosage amounts of LC, CC, and SH at the time of final evaluation were 0.87 g, 2.30 g, and 0.99 g, respectively. After the application of LC, serum phosphate as well as serum calcium controls were significantly improved, and the amounts of active vitamin D agents applied was significantly increased. In conclusion, LC is useful in managing serum phosphorus levels (P levels), and little incidence of hypercalcemia suggests favorable concomitant use with active vitamin D agents in LC therapy.

  15. Preparation of multi-functional superhydrophobic lanthanum surface on carbon steel via facile electrochemical method

    NASA Astrophysics Data System (ADS)

    Chen, Xi; He, Yi; Fan, Yi; Yang, Qiangbin; Li, Han

    2016-12-01

    We have constructed a superhydrophobic surface with lanthanum palmitate on carbon steel via a facile one-step electrodeposition. The morphology and chemical composition of the superhydrophobic surface were characterized by field-emission scanning electron microscopy with attached energy dispersive X-ray spectrum, Fourier transform infrared spectra and X-ray photoelectron spectroscopy, respectively. The as-prepared surface with hierarchical structure has a largest contact angle of 160° ± 0.5° and a lowest sliding angle of 2° ± 0.5°. We found that both high electrodeposition potential and high concentrations lanthanum nitrate can accelerate the formation of superhydrophobic film. The electrochemical measurements demonstrated that the superhydrophobic surface exhibited excellent anti-corrosion performance in 3.5 wt% NaCl solution. Moreover, we also investigated the chemical stability, self-cleaning and oil/water separation of the superhydrophobic film. We believe that the facile fabrication method provides a promising strategy to fabricate multi-functional superhydrophobic surface with lanthanide series rare-earth elements on kinds of substrates.

  16. Structural, microstructural and vibrational characterization of apatite-type lanthanum silicates prepared by mechanical milling

    NASA Astrophysics Data System (ADS)

    Rodríguez-Reyna, E.; Fuentes, A. F.; Maczka, M.; Hanuza, J.; Boulahya, K.; Amador, U.

    2006-02-01

    Apatite-type lanthanum silicates have been successfully prepared at room temperature by dry milling hexagonal A-La 2O 3 and either amorphous or low cristobalite SiO 2. Milling a stochiometric mixture of these chemicals in a planetary ball mill with a moderate rotating disc speed (350 rpm), allows the formation of the target phase after only 3 h although longer milling times are needed to eliminate all SiO 2 and La 2O 3 traces. Thus, the mechanically activated chemical reaction proceeds faster when using amorphous silica instead of low cristobalite as silicon source and pure phases are obtained after only 9 and 18 h, respectively. As obtained powder phases are not amorphous and show an XRD pattern as well as IR and Raman bands characteristic of the lanthanum silicate. The domain size of the as-prepared phases varies gradually with the temperature of post-milling thermal treatment with activation energies of about 26(8) and 52(10) kJ mol -1 K -1 for the apatites obtained from amorphous silica and low-cristobalite, respectively. These values suggest crystallite growth to be favored when using amorphous silica as reactant.

  17. Solution processed lanthanum aluminate gate dielectrics for use in metal oxide-based thin film transistors

    SciTech Connect

    Esro, M.; Adamopoulos, G.; Mazzocco, R.; Kolosov, O.; Krier, A.; Vourlias, G.; Milne, W. I.

    2015-05-18

    We report on ZnO-based thin-film transistors (TFTs) employing lanthanum aluminate gate dielectrics (La{sub x}Al{sub 1−x}O{sub y}) grown by spray pyrolysis in ambient atmosphere at 440 °C. The structural, electronic, optical, morphological, and electrical properties of the La{sub x}Al{sub 1−x}O{sub y} films and devices as a function of the lanthanum to aluminium atomic ratio were investigated using a wide range of characterization techniques such as UV-visible absorption spectroscopy, impedance spectroscopy, spectroscopic ellipsometry, atomic force microscopy, x-ray diffraction, and field-effect measurements. As-deposited LaAlO{sub y} dielectrics exhibit a wide band gap (∼6.18 eV), high dielectric constant (k ∼ 16), low roughness (∼1.9 nm), and very low leakage currents (<3 nA/cm{sup 2}). TFTs employing solution processed LaAlO{sub y} gate dielectrics and ZnO semiconducting channels exhibit excellent electron transport characteristics with hysteresis-free operation, low operation voltages (∼10 V), high on/off current modulation ratio of >10{sup 6}, subthreshold swing of ∼650 mV dec{sup −1}, and electron mobility of ∼12 cm{sup 2} V{sup −1} s{sup −1}.

  18. Antineoplastic activity of new lanthanide (cerium, lanthanum and neodymium) complex compounds.

    PubMed

    Kostova, Irena; Kostova, Raina; Momekov, Georgi; Trendafilova, Natasha; Karaivanova, Margarita

    2005-01-01

    Cerium (III), lanthanum (III) and neodymium (III) complexes with 3,3'-benzylidenebis[4-hydroxycoumarin] were synthesized in view of their application as cytotoxic agents. The complexes were characterized by different physicochemical methods: elemental analysis, mass spectrometry, 1H NMR, 13C NMR and IR spectroscopy. The spectra of the complexes were interpreted on the basis of comparison with the spectrum of the free ligand. The vibrational analysis showed that in the complexes the ligand coordinated to the metal ion through both deprotonated hydroxyl groups; however, participation of the carbonyl groups in the coordination to the metal ion was also suggested. The evaluation of the cytotoxic activity of the novel lanthanide complexes on HL-60 myeloid cells revealed that they are potent cytotoxic agents. The cerium complex was found to exhibit superior activity in comparison to the lanthanum and neodymium coordination compounds, the latter being the least active. Our data give us reason to conclude that the newly synthesized lanthanide complexes should be submitted to further more detailed pharmacological and toxicological evaluation.

  19. Thermal stability and microstructure of catalytic alumina composite support with lanthanum species

    NASA Astrophysics Data System (ADS)

    Ozawa, Masakuni; Nishio, Yoshitoyo

    2016-09-01

    Lanthanum (La) modified γ-alumina composite was examined for application toward thermostable catalytic support at elevated temperature. La added alumina was prepared through an aqueous process using lanthanum (III) nitrate and then characterized by surface area measurement, X-ray powder diffraction (XRD), differential thermal analysis (DTA), scanning electron microscope (SEM), transmission electron microscope (TEM), X-ray photoemission spectroscopy (XPS) and surface desorption of CO2. It was found that the properties depended on the La content and heat treatment temperatures. The characterization of the surface, structural and chemical properties of La-Al2O3 showed the existence of a strong interaction between the La species and alumina via formation of new phase and modified surface in Al2O3 samples. LaAlO3 nanoparticle formed among alumina particles by the solid phase reaction of Al2O3 and La2O3. The increase of the surface basicity of La modified alumina was demonstrated using CO2 temperature programmed desorption experiments. The controlled surface interaction between La oxide and alumina provide the unique surface and structural properties of the resulting mixed oxides as catalysts and catalytic supports.

  20. Ionic liquid-mediated synthesis of meso-scale porous lanthanum-transition-metal perovskites with high CO oxidation performance

    SciTech Connect

    Lu, Hanfeng; Zhang, Pengfei; Qiao, Zhen-An; Zhang, Jinshui; Zhu, Huiyuan; Chen, Jihua; Chen, Yinfei; Dai, Sheng

    2015-01-01

    Lanthanum-transition-metal perovskites with robust meso-scale porous frameworks (meso-LaMO3) are synthesized through use of ionic liquids. The resultant samples demonstrate a rather high activity for CO oxidation, by taking advantage of unique nanostructure-derived benefits. This synthesis strategy opens up a new opportunity for preparing functional mesoporous complex oxides of various compositions.

  1. Ionic liquid-mediated synthesis of meso-scale porous lanthanum-transition-metal perovskites with high CO oxidation performance

    DOE PAGES

    Lu, Hanfeng; Zhang, Pengfei; Qiao, Zhen-An; ...

    2015-01-01

    Lanthanum-transition-metal perovskites with robust meso-scale porous frameworks (meso-LaMO3) are synthesized through use of ionic liquids. The resultant samples demonstrate a rather high activity for CO oxidation, by taking advantage of unique nanostructure-derived benefits. This synthesis strategy opens up a new opportunity for preparing functional mesoporous complex oxides of various compositions.

  2. Enhancement of thermal shock resistance of reaction sintered mullite–zirconia composites in the presence of lanthanum oxide

    SciTech Connect

    Kumar, P.; Nath, M.; Ghosh, A.; Tripathi, H.S.

    2015-03-15

    Mullite–zirconia composites containing 20 wt.% zirconia were prepared by reaction sintering of zircon flour, sillimanite beach sand and calcined alumina. 0 to 8 mol% of La{sub 2}O{sub 3} with respect to zirconia was used as sintering aid. The effect of additive on the various physical, microstructures, mechanical and thermo-mechanical properties was studied. Quantitative phase analysis shows the change in tetragonal zirconia content with incorporation of lanthanum oxide. La{sub 2}O{sub 3} addition has significantly improved the thermal shock resistance of the samples. Samples without additive retained only 20% of initial flexural strength after 5 cycles, whereas samples containing 5 mol% La{sub 2}O{sub 3} retained almost 78% of its initial flexural strength even after 15 thermal shock cycles. - Highlights: • Mullite–zirconia composites were prepared by reaction sintering route utilizing zircon and sillimanite beach sand. • Lanthanum oxide was used as sintering aid. • The presence of lanthanum oxide decreased the densification temperature. • Lanthanum oxide significantly improved the thermal shock resistance of the composites.

  3. [CKD-MBD (Chronic Kidney Disease-Mineral and Bone Disorder). Lanthanum carbonate and new phosphate binders in patients with chronic kidney disease].

    PubMed

    Negi, Shigeo; Shigematsu, Takashi

    2010-07-01

    Hyperphosphatemia is a serious complication which has been linked with an increased risk of cardiovascular mortality in patients with chronic kidney disease. Lanthanum carbonate is a novel non-calcium, non-aluminum phosphate-binding agent, and has approved for clinical use in patients on hemodialysis in Japan on March in 2009. Compared to calcium carbonate and sevelamer hydrochloride, lanthanum carbonate is a powerful phosphate binder. There is no evidence of bone toxicity and neurotoxicity of lanthanum carbonate previously reported for aluminium hydroxide. However, further studies are needed to address the longer term toxic effect on bone and other organs.

  4. Crystallization behavior of a barium titanate tellurite glass doped with Eu3+ and Er3+

    NASA Astrophysics Data System (ADS)

    Ferreira, Elivelton Alves; Cassanjes, Fábia Castro; Poirier, Gael

    2013-04-01

    The main objective of this work has been to investigate the crystallization behavior of the glass composition 70TeO2-15BaO-15TiO2 doped with Eu3+ and Er3+ in order to check the possibility of obtaining transparent glass-ceramics containing rare earth-doped BaTiO3 nanocrystals. Glass samples with the ternary composition 70TeO2-15BaO-15TiO2 were synthesized by the melt-quenching method and doped with 0.1% of Eu3+ and Er3+. Thermal properties were investigated by DTA and heat-treatments were applied between Tg and Tx to induce the controlled crystallization of these glasses. One-step and two-step heat treatments were tested and the final glass-ceramics characterized by X-ray diffraction and UV-Vis absorption. It has been shown that transparent glass-ceramics can be obtained after heat-treatment but barium titanate BaTiO3 is hardly precipitated without coprecipitation of another crystalline phase identified as an isostructure of lanthanum tellurate. In addition, the crystalline volume fraction is relatively small in these transparent samples. Finally, Gold doping has been shown to be very effective to promote a volume nucleation and preferential crystallization of BaTiO3 over the other crystalline phases.

  5. Influence of La doping on structural and dielectric properties of SrBi{sub 2}Nb{sub 2}O{sub 9} ceramics

    SciTech Connect

    Verma, Maya; Sreenivas, K.; Gupta, Vinay

    2009-01-15

    Lanthanum doped SrBi{sub 2}Nb{sub 2}O{sub 9} ceramics with the chemical formula SrBi{sub 2-x}La{sub x}Nb{sub 2}O{sub 9} (SBLN) (x=0-0.5) have been prepared through conventional solid state route. X-ray diffraction reveals the shrinkage of unit cell of strontium bismuth niobate with incorporation of La{sup 3+} dopant, having no lone pair electrons. Shifting of Raman phonon modes indicates the reduced rattling space of NbO{sub 6} octahedra with increase in La doping concentration. Further, the softening of lowest frequency phonon mode with increasing x in SBLN shows the transition from ferroelectric to paraelectric at room temperature. The dielectric properties for all the compositions are studied as a function of temperature (25 to 500 deg. C) over the frequency range of 10 kHz-1 MHz. With increase in lanthanum doping concentration the phase transition becomes diffused and transition temperature gets shifted toward lower temperature. A phase transition from normal ferroelectric to paraelectric has been observed via relaxor-type ferroelectrics with increase in x. The frequency dependence of transition temperature was studied in terms of Vogel-Fulcher relation for SBLN (x=0.4)

  6. Development of a virus concentration method using lanthanum-based chemical flocculation coupled with modified membrane filtration procedures.

    PubMed

    Zhang, Yanyan; Riley, Lela K; Lin, Mengshi; Purdy, Gregory A; Hu, Zhiqiang

    2013-06-01

    Direct membrane filtration is often used to concentrate viruses in water but it may suffer from severe membrane fouling and clogging. Here, a lanthanum-based flocculation method coupled with modified membrane filtration procedures was developed and evaluated to detect viruses in large volume (40 L) water samples. The lanthanum-based flocculation method could easily reduce the water sample volume by a factor of 40. Additional volume reduction was achieved by a two-step membrane filtration approach. First, selected membrane filters (including 1MDS electropositive filters and nitrocellulose electronegative filters-Millipore HATF filters) were used to reduce water sample volume further and compare their efficiencies in virus recovery. The Mg²⁺-modified HATF membrane performed better on MS2 retention with an average virus recovery of 83.4% (±4.5% [standard deviation]). After HATF membrane filtration and elution, centrifugal ultrafiltration through a 30 kDa cut-off membrane resulted in an overall concentration factor of 20,000. Results from the infectivity assay showed that the MS2 recovery efficiencies from the NanoCeram- and 1MDS-based direct filtration and the lanthanum-based concentration coupled with the modified filtration procedure were 10.1% (±1.0%), 3.3% (±0.1%), and 17.5% (±1.1%), respectively. Results from the PCR analysis showed that the virus recoveries of the lanthanum-based method were 20.6% (±2.9%) and 19.5% (±3.4%) for MS2 and adenovirus, respectively, while no adenovirus could be detected through the NanoCeram- and 1MDS-based direct filtration. The lanthanum-based concentration method coupled with modified membrane filtration procedures is therefore a promising method for detecting waterborne viruses.

  7. Lake responses following lanthanum-modified bentonite clay (Phoslock®) application: an analysis of water column lanthanum data from 16 case study lakes.

    PubMed

    Spears, Bryan M; Lürling, Miquel; Yasseri, Said; Castro-Castellon, Ana T; Gibbs, Max; Meis, Sebastian; McDonald, Claire; McIntosh, John; Sleep, Darren; Van Oosterhout, Frank

    2013-10-01

    Phoslock(®) is a lanthanum (La) modified bentonite clay that is being increasingly used as a geo-engineering tool for the control of legacy phosphorus (P) release from lake bed sediments to overlying waters. This study investigates the potential for negative ecological impacts from elevated La concentrations associated with the use of Phoslock(®) across 16 case study lakes. Impact-recovery trajectories associated with total lanthanum (TLa) and filterable La (FLa) concentrations in surface and bottom waters were quantified over a period of up to 60 months following Phoslock(®) application. Both surface and bottom water TLa and FLa concentrations were <0.001 mg L(-1) in all lakes prior to the application of Phoslock(®). The effects of Phoslock(®) application were evident in the post-application maximum TLa and FLa concentrations reported for surface waters between 0.026 mg L(-1)-2.30 mg L(-1) and 0.002 mg L(-1) to 0.14 mg L(-1), respectively. Results of generalised additive modelling indicated that recovery trajectories for TLa and FLa in surface and bottom waters in lakes were represented by 2nd order decay relationships, with time, and that recovery reached an end-point between 3 and 12 months post-application. Recovery in bottom water was slower (11-12 months) than surface waters (3-8 months), most probably as a result of variation in physicochemical conditions of the receiving waters and associated effects on product settling rates and processes relating to the disturbance of bed sediments. CHEAQS PRO modelling was also undertaken on 11 of the treated lakes in order to predict concentrations of La(3+) ions and the potential for negative ecological impacts. This modelling indicated that the concentrations of La(3+) ions will be very low (<0.0004 mg L(-1)) in lakes of moderately low to high alkalinity (>0.8 mEq L(-1)), but higher (up to 0.12 mg L(-1)) in lakes characterised by very low alkalinity. The effects of elevated La(3+) concentrations following

  8. Electroinduced structural change- and random walks-based impact on the light emission in Er3+/Yb3+ doped (Pb,La)(Zr,Ti)O3 ceramics

    NASA Astrophysics Data System (ADS)

    Xu, L.; Zhang, J.; Zhang, S.; Xu, C.; Zou, Y. K.; Zhao, H.

    2013-06-01

    Remarkable enhancement/reduction of light emission and competition among different wavebands with rare earth doped lanthanum lead zirconate titanate ceramics were observed in a corona atmosphere caused by an externally applied electric field. Quantum-mechanical analyses, based on variation of structural symmetry of the unit cell and hence the crystal field due to electrostriction, were given to elucidate the effect. Apart from the symmetry of crystal field, the obvious contribution from the optoenergy storage and weak localization of light involved were discussed. These results are promising in designing and implementation of lasers and sensors.

  9. The Anti-Doping Movement.

    PubMed

    Willick, Stuart E; Miller, Geoffrey D; Eichner, Daniel

    2016-03-01

    Historical reports of doping in sports date as far back as the ancient Greek Olympic Games. The anti-doping community considers doping in sports to be cheating and a violation of the spirit of sport. During the past century, there has been an increasing awareness of the extent of doping in sports and the health risks of doping. In response, the anti-doping movement has endeavored to educate athletes and others about the health risks of doping and promote a level playing field. Doping control is now undertaken in most countries around the world and at most elite sports competitions. As athletes have found new ways to dope, however, the anti-doping community has endeavored to strengthen its educational and deterrence efforts. It is incumbent upon sports medicine professionals to understand the health risks of doping and all doping control processes.

  10. Polarization induced doped transistor

    SciTech Connect

    Xing, Huili; Jena, Debdeep; Nomoto, Kazuki; Song, Bo; Zhu, Mingda; Hu, Zongyang

    2016-06-07

    A nitride-based field effect transistor (FET) comprises a compositionally graded and polarization induced doped p-layer underlying at least one gate contact and a compositionally graded and doped n-channel underlying a source contact. The n-channel is converted from the p-layer to the n-channel by ion implantation, a buffer underlies the doped p-layer and the n-channel, and a drain underlies the buffer.

  11. Synthesis of La and Nb doped PZT powder by the gel-combustion method

    NASA Astrophysics Data System (ADS)

    Cernea, M.; Montanari, G.; Galassi, C.; Costa, A. L.

    2006-03-01

    Lanthanum and niobium doped PZT with composition (Pb0.93La0.07)[(Zr0.60Ti0.40)]0.9825Nb0.0175O3 (PZTLN) was prepared by the gel-combustion method. A precursor sol was obtained from lead nitrate, zirconyl nitrate, lanthanum oxide, peroxo-citrato-niobium and a peroxo-citrate complex of titanium isopropoxide as starting precursors. Various molar ratios of citrate/nitrate (CA/NO3- = 1.3, 0.36 and 0.09) were used to prepare very fine powders of PZTLN. The gels resulting from these sols were transformed into powders by an auto-combustion process at <=400 °C. The powders consisted of rhombohedral PZT (PbZr0.60Ti0.40O3), pyrochlore (Pb2Ti2O6) and lead carbonate (Pb2O·CO3) phases. The pure rhombohedral phase is found in PZTLN pellets sintered at 1100 °C for all citrate/nitrate ratios. Titanium and niobium precursors were modified with peroxo radicals. During the gel-combustion reaction, the temperature of the gel increases, leading to lead evaporation. The loss of lead as well as the particle size increases as the CA/NO3- ratio decreases. The smallest grained powder (about 50 nm) was obtained with the ratio CA/NO3- equal to 0.09.

  12. Effects of lanthanum carbonate on vascular calcification in elderly maintenance hemodialysis patients.

    PubMed

    Wang, Xiao-Hui; Zhang, Xin; Mu, Chang-Jun; He, Yong; Peng, Qing-Ping; Yang, Guo-Sheng; Li, Ming-Mei; Liu, Duan; Li, Jing; Ding, Guo-Hua

    2015-08-01

    The effect of lanthanum carbonate on abdominal aortic calcification (AAC) in the elderly maintenance hemodialysis (MHD) patients was investigated. Fifty-four cases subjected to routine MHD complicated with skin pruritus admitted to our hospital were selected and randomly divided into case group (n=28) and control group (n=26). The control group was given routine MHD alone. The case group was given lanthanum carbonate additionally on the basis of routine MHD. The changes of itching degrees at first and third month, and serum calcium, phosphorus, calcium-phosphorus products, intact parathyroid hormone (iPTH) levels and AAC scores at third month after treatments were compared between the two groups. The correlation between calcium-phosphorus products and AAC scores was also analyzed. There was no significant difference in the baseline of blood urea nitrogen (BUN), serum creatinine (Scr), uric acid, albumin, hemoglobin, C reactive protein (CRP), low density lipoprotein (LDL), high density lipoprotein (HDL), triglyceride, total cholesterol between case group and control group (P>0.05 for all). There was also no significant difference in the baseline itching scores between the case group and the control group (P>0.05). At 1st and 3rd month after treatment, the itching scores in the case group were 14.2 ± 3.2 and 10.5 ± 2.3, respectively, which were significantly lower than the baseline and those in the control group (P<0.05 for all). At 1st and 3rd month after treatment, the itching scores in the control group were 23.6 ± 5.9 and 24.8 ± 6.3, respectively, which were significantly higher than the baseline (P<0.05). There was no significant difference in the baseline of serum calcium, phosphorus, calcium-phosphorus products, iPTH levels between the case group and control group (P>0.05). At 3rd month after treatment, serum phosphorus, calcium-phosphorus products and iPTH levels in the case group were decreased significantly as compared with the baseline (P<0.05), and

  13. Microcalorimetric determination of the thermodynamics of formation of the mono- and bi-sulfato complexes of lanthanum in aqueous solutions between 25 and 55 degrees C

    SciTech Connect

    Simpson, C.; Matijevic, E.

    1987-05-01

    Using a differential microcalorimeter, the formation constants and enthalpies of formation of the mono- and bi-sulfato complexes of lanthanum ion have been evaluated for aqueous acidic solutions over a temperature range of 25 to 55/sup 0/C.

  14. Static and high-frequency magnetic properties of Fe and Cr substituted lanthanum manganites

    NASA Astrophysics Data System (ADS)

    Srinivasan, G.; Hanna, D.; Suryanarayanan, R.; Berthon, J.

    2000-03-01

    Studies aimed at the nature of magnetic interactions in Fe and Cr substituted lanthanum deficient manganites, La 0.88Mn 1- xFe xO 3 ( x=0-0.15) and La 0.88Mn 1- yCr yO 3 ( y=0-0.175) are reported. The oxides order ferromagnetically for the entire range of x- and y-values. A decrease in the Curie temperature Tc with increasing substitution is observed for both compounds, but the decrease in Tc is large for Fe substitution. A large decrease was also seen in the low-temperature magnetic moment of Fe substituted samples. The data indicate possible ferromagnetic ordering of Cr and antiferromagnetic ordering of Fe moments in the oxides. Ferromagnetic resonance studies indicate (i) strong spin-lattice effects in the paramagnetic state, (ii) valence-exchange effects in the ferromagnetic state, and (iii) possible microscopic inhomogeneities in Cr-substituted samples

  15. Processing and structural properties of random oriented lead lanthanum zirconate titanate thin films

    SciTech Connect

    Araújo, E.B.; Nahime, B.O.; Melo, M.; Dinelli, F.; Tantussi, F.; Baschieri, P.; Fuso, F.; Allegrini, M.

    2015-01-15

    Highlights: • Pyrochlore phase crystallizes near the bottom film-electrode interface. • PLZT films show a non-uniform microstrain and crystallite size in depth profile. • Complex grainy structure leads to different elastic modulus at the nanoscale. - Abstract: Polycrystalline lead lanthanum zirconate titanate (PLZT) thin films have been prepared by a polymeric chemical route to understand the mechanisms of phase transformations and map the microstructure and elastic properties at the nanoscale in these films. X-ray diffraction, atomic force microscopy (AFM) and ultrasonic force microscopy (UFM) have been used as investigative tools. On one side, PLZT films with mixed-phase show that the pyrochlore phase crystallizes predominantly in the bottom film-electrode interface while a pure perovskite phase crystallizes in top film surface. On the contrary, pyrochlore-free PLZT films show a non-uniform microstrain and crystallite size along the film thickness with a heterogeneous complex grainy structure leading to different elastic properties at nanoscale.

  16. Stabilization of ambient sensitive atomic layer deposited lanthanum aluminates by annealing and in situ capping

    NASA Astrophysics Data System (ADS)

    Swerts, J.; Gielis, S.; Vereecke, G.; Hardy, A.; Dewulf, D.; Adelmann, C.; Van Bael, M. K.; Van Elshocht, S.

    2011-03-01

    We have studied the effect of air exposure on lanthanum aluminates (LaAlOx) deposited by atomic layer deposition. Fourier transform infrared spectroscopy and thermal desorption spectroscopy of as-deposited LaAlOx showed that H2O is absorbed during air exposure and that the amount of absorbed H2O increases with increasing La atomic percent. C was found to be incorporated already during deposition in the form of carbonates. H2O and CO2 are outgassed during postdeposition annealing in an inert atmosphere. After a 700 °C postdeposition anneal, the LaAlOx becomes resistant against H2O absorption due to film densification. Alternatively, in situ capping of the LaAlOx with a ˜2 nm thin Al2O3 film protects the LaAlOx against H2O absorption, but it also hinders the outgassing of the C contaminants during a postdeposition anneal.

  17. Large area directly heated lanthanum hexaboride cathode structure having predetermined emission profile

    DOEpatents

    Leung, Ka-Ngo; Gordon, K.C.; Kippenhan, D.O.; Purgalis, P.; Moussa, D.; Williams, M.D.; Wilde, S.B.; West, M.W.

    1987-10-16

    A large area directly heated lanthanum hexaboride (LaB/sub 6/) cathode system is disclosed. The system comprises a LaB/sub 6/ cathode element generally circular in shape about a central axis. The cathode element has a head with an upper substantially planar emission surface, and a lower downwardly and an intermediate body portion which diminishes in cross-section from the head towards the base of the cathode element. A central rod is connected to the base of the cathode element and extends along the central axis. Plural upstanding spring fingers are urged against an outer peripheral contact surface of the head end to provide a mechanical and electrical connection to the cathode element. 7 figs

  18. Large area directly heated lanthanum hexaboride cathode structure having predetermined emission profile

    DOEpatents

    Leung, Ka-Ngo; Gordon, Keith C.; Kippenham, Dean O.; Purgalis, Peter; Moussa, David; Williams, Malcom D.; Wilde, Stephen B.; West, Mark W.

    1989-01-01

    A large area directly heated lanthanum hexaboride (LaB.sub.6) cathode system (10) is disclosed. The system comprises a LaB.sub.6 cathode element (11) generally circular in shape about a central axis. The cathode element (11) has a head (21) with an upper substantially planar emission surface (23), and a lower downwardly and an intermediate body portion (26) which diminishes in cross-section from the head (21) towards the base (22) of the cathode element (11). A central rod (14) is connected to the base (22) of the cathode element (11) and extends along the central axis. Plural upstanding spring fingers (37) are urged against an outer peripheral contact surface (24) of the head end (21) to provide a mechanical and electrical connection to the cathode element (11).

  19. Effect of Gun Current on Electrical Properties of Atmospheric Plasma-Sprayed Lanthanum Silicate Coatings

    NASA Astrophysics Data System (ADS)

    Gao, Wei; Liao, Han-Lin; Coddet, Christian

    2013-10-01

    Apatite-type lanthanum silicate (ATLS) electrolyte coatings for use in intermediate-temperature solid oxide fuel cells were deposited by atmospheric plasma spraying (APS). Plasma-sprayed coatings with typical composition La10(SiO4)6O3 exhibiting good densification and high oxide ionic conductivity were obtained by properly adjusting the spraying parameters, particularly the gun current. The highest obtained ionic conductivity value of 3.3 mS/cm at 1,173 K in air is comparable to other ATLS conductors. This work demonstrated empirically that utilization of the APS technique is feasible to synthesize dense La10(SiO4)6O3 electrolyte coatings using gun currents within an unusually broad range.

  20. Chemical solution deposition of the highly c-axis oriented apatite type lanthanum silicate thin films.

    PubMed

    Hori, Shigeo; Takatani, Yasuhiro; Kadoura, Hiroaki; Uyama, Takeshi; Fujita, Satoru; Tani, Toshihiko

    2015-10-28

    Highly c-axis oriented apatite-type lanthanum silicate (LSO) thin films were fabricated by a simple solution coating method. In the solution coating method, LSO thin films are obtained by crystallization of initially deposited amorphous LSO precursor thin films. The degree of orientation was influenced by the precursor morphologies and a dense LSO precursor led to a high c-axis orientation perpendicular to the substrate. The oriented LSO thin films were composed of columnar grains with a single crystal orientation over the entire film thickness. In-plane orientation was not detected, which indicates that the c-axis orientation of the LSO thin films can be attributed to self-orientation.