EPR-study of reversible oxygenation process of coordination compounds of cobalt(II) with S-substituted N1,N4-di(salicylidene)-isothiosemicarbazides

International Nuclear Information System (INIS)

Gerbeleu, N.V.; Revenko, M.D.; Rusu, V.G.; Shames, A.T.

1987-01-01

The reaction between molecular oxygen and coordination compounds of cobalt(II) with S-substituted N 1 ,N 4 -di(salicylidene)isothiosemicarbazides in dimethyl sulfoxide solution was studied by the EPR method. It was found that paramagnetic monomeric adducts and diamagnetic μ-peroxo-dimers are formed. The spin-Hamiltonian parameters of the EPR spectra of the initial cobalt complexes, as well as of the paramagnetic adducts were determined. The nature of the Co-O 2 bond is discussed

Migratory Insertion of Hydrogen Isocyanide in the Pentacyano(methyl)cobaltate(III) Anion

DEFF Research Database (Denmark)

Kofod, Pauli; Harris, Pernille Hanne; Larsen, Sine

2003-01-01

The preparation of the pentacyano(iminiumacetyl)cobaltate(III) anion and its N-methyl and N,N-dimethyl derivatives is reported. The iminiumacetyl group is formed by migratory insertion of cis hydrogen isocyanide in the pentacyano(methyl)cobaltate(III) anion. The new compounds have been spectrosco......The preparation of the pentacyano(iminiumacetyl)cobaltate(III) anion and its N-methyl and N,N-dimethyl derivatives is reported. The iminiumacetyl group is formed by migratory insertion of cis hydrogen isocyanide in the pentacyano(methyl)cobaltate(III) anion. The new compounds have been...

Nitrogen-doped carbon-supported cobalt-iron oxygen reduction catalyst

Science.gov (United States)

Zelenay, Piotr; Wu, Gang

2014-04-29

A Fe--Co hybrid catalyst for oxygen reaction reduction was prepared by a two part process. The first part involves reacting an ethyleneamine with a cobalt-containing precursor to form a cobalt-containing complex, combining the cobalt-containing complex with an electroconductive carbon supporting material, heating the cobalt-containing complex and carbon supporting material under conditions suitable to convert the cobalt-containing complex and carbon supporting material into a cobalt-containing catalyst support. The second part of the process involves polymerizing an aniline in the presence of said cobalt-containing catalyst support and an iron-containing compound under conditions suitable to form a supported, cobalt-containing, iron-bound polyaniline species, and subjecting said supported, cobalt-containing, iron bound polyaniline species to conditions suitable for producing a Fe--Co hybrid catalyst.

EPR-study of reversible oxygenation process of coordination compounds of cobalt(II) with S-substituted N/sup 1/,N/sup 4/-di(salicylidene)-isothiosemicarbazides

Energy Technology Data Exchange (ETDEWEB)

Gerbeleu, N.V.; Revenko, M.D.; Rusu, V.G.; Shames, A.T.

1987-09-01

The reaction between molecular oxygen and coordination compounds of cobalt(II) with S-substituted N/sup 1/,N/sup 4/-di(salicylidene)isothiosemicarbazides in dimethyl sulfoxide solution was studied by the EPR method. It was found that paramagnetic monomeric adducts and diamagnetic ..mu..-peroxo-dimers are formed. The spin-Hamiltonian parameters of the EPR spectra of the initial cobalt complexes, as well as of the paramagnetic adducts were determined. The nature of the Co-O/sub 2/ bond is discussed.

Synthesis and butadiene polymerization behaviors of cationic cobalt-based catalyst

Directory of Open Access Journals (Sweden)

Li Liu

2017-01-01

Full Text Available A series of cationic cobalt-based compounds bearing different neutral N-bearing ligands (1,10-phenanthroline, bipyridine, benzimidazole, terpyridine and anionic ligands (trifluoromethanesulfonate, methanesulfonate were synthesized and the simple compound, Co(Phen2Cl2, was also prepared as a reference compound. All the compounds were characterized along with infrared spectra analysis and some of them were further confirmed by single crystal X-ray crystallographic analysis. Upon activation with ethylaluminum sesquichloride, these cationic cobalt(II compounds showed high catalytic activities for butadiene polymerization. The detailed investigations were carried out to disclose the influence of various polymerization conditions, sterical and electronic parameters of the ligands on their performing activities of the compounds.

The cytotoxicity and genotoxicity of soluble and particulate cobalt in human lung fibroblast cells

Energy Technology Data Exchange (ETDEWEB)

Smith, Leah J.; Holmes, Amie L. [Wise Laboratory of Environmental and Genetic Toxicology, University of Southern Maine, 96 Falmouth St., P.O. Box 9300, Portland, ME 04101-9300 (United States); Maine Center for Environmental Toxicology and Health, University of Southern Maine, 96 Falmouth St., P.O. Box 9300, Portland, ME 04101-9300 (United States); Department of Applied Medical Science, University of Southern Maine, 96 Falmouth St., P.O. Box 9300, Portland, ME 04101-9300 (United States); Kandpal, Sanjeev Kumar; Mason, Michael D. [Department of Chemical and Biological Engineering, University of Maine, Orono, ME (United States); Zheng, Tongzhang [Department of Environmental Health Sciences, Yale School of Public Health, New Haven, CT (United States); Wise, John Pierce, E-mail: John.Wise@usm.maine.edu [Wise Laboratory of Environmental and Genetic Toxicology, University of Southern Maine, 96 Falmouth St., P.O. Box 9300, Portland, ME 04101-9300 (United States); Maine Center for Environmental Toxicology and Health, University of Southern Maine, 96 Falmouth St., P.O. Box 9300, Portland, ME 04101-9300 (United States); Department of Applied Medical Science, University of Southern Maine, 96 Falmouth St., P.O. Box 9300, Portland, ME 04101-9300 (United States)

2014-08-01

Cobalt exposure is increasing as cobalt demand rises worldwide due to its use in enhancing rechargeable battery efficiency, super-alloys, and magnetic products. Cobalt is considered a possible human carcinogen with the lung being a primary target. However, few studies have considered cobalt-induced toxicity in human lung cells. Therefore, in this study, we sought to determine the cytotoxicity and genotoxicity of particulate and soluble cobalt in human lung cells. Cobalt oxide and cobalt chloride were used as representative particulate and soluble cobalt compounds, respectively. Exposure to both particulate and soluble cobalt induced a concentration-dependent increase in cytotoxicity, genotoxicity, and intracellular cobalt ion levels. Based on intracellular cobalt ion levels, we found that soluble cobalt was more cytotoxic than particulate cobalt while particulate and soluble cobalt induced similar levels of genotoxicity. However, soluble cobalt induced cell cycle arrest indicated by the lack of metaphases at much lower intracellular cobalt concentrations compared to cobalt oxide. Accordingly, we investigated the role of particle internalization in cobalt oxide-induced toxicity and found that particle-cell contact was necessary to induce cytotoxicity and genotoxicity after cobalt exposure. These data indicate that cobalt compounds are cytotoxic and genotoxic to human lung fibroblasts, and solubility plays a key role in cobalt-induced lung toxicity. - Highlights: • Particulate and soluble cobalt are cytotoxic and genotoxic to human lung cells. • Soluble cobalt induces more cytotoxicity compared to particulate cobalt. • Soluble and particulate cobalt induce similar levels of genotoxicity. • Particle-cell contact is required for particulate cobalt-induced toxicity.

SYNTHESIS AND ANTITUMOR ACTIVITY OF COPPER, NICKEL AND COBALT COORDINATION COMPOUNDS WITH 1-(2-HYDROXYPHENYL)ETHANONE N(4)-ALLYL-3-THIOSEMICARBAZONE

OpenAIRE

Vasilii GRAUR; Serghei SAVCIN; Victor TSAPKOV; Aurelian GULEA

2015-01-01

The paper presents the synthesis of the ligand 1-(2-hydroxyphenyl)ethanone N(4)-allyl-3-thiosemicarbazone (H2L) and six coordination compounds of copper, nickel and cobalt with this ligand. The structure of thiosemicarbazone H2L was studied using 1H and 13С NMR spectroscopy. The synthesized coordination compounds were studied using elemental analysis, gravimetric analysis of water content, molar conductivity, and magnetochemistry. For H2L the antitumor activity towards human leukemia HL-60 ce...

Rare earth intermetallic compounds produced by a reduction-diffusion process

International Nuclear Information System (INIS)

Cech, R.E.

1975-01-01

A reduction-diffusion process is given for producing novel rare earth intermetallic compounds, such as cobalt--rare earth intermetallic compounds, especially compounds useful in preparing permanent magnets. A particulate mixture of rare earth metal halide, cobalt and calcium hydride is heated to effect reduction of the rare earth metal halide and to diffuse the resulting rare earth metal into the cobalt to form the intermetallic compound

Diffusion of samarium into cobalt in the reduction-diffusion process

International Nuclear Information System (INIS)

Freitas Nogueira, P. de; Neto, F.B.; Landgraf, F.J.G.

1998-01-01

The presence of metallic cobalt in samarium-cobalt powders is a major cause for low magnetic properties in magnets. This paper intends to investigate the effect of time and temperature in the microstructure of powders produced by reduction-diffusion. This process, developed for the production of rare earth-transition metal alloys, consists on the reduction of the rare earth oxide with metallic calcium (or calcium hydride) and its subsequent diffusion into the cobalt particle. In the present work, a mixture of samarium oxide, cobalt powder and metallic calcium was heated to 1100 or 1200 C for 2 or 4 hours in a tubular furnace under one atmosphere of purified argon. The material thereof obtained, a sintered mass is disintegrated by aqueous crepitation. The powder was evaluated in terms of its chemical composition, its samarium yield and the intermetallic compounds present. The samarium, oxygen and calcium content of the powders produced were adequate for magnet production. However, despite the massive formation of the SmCo 5 compound after 2 hours at 1100 C, final homogeneity is attained only after 4 hours at 1200 C, with the presence of SmCo 5 and Sm 2 Co 7 and the absence of the Sm 5 Co 19 compound. Also, metallic cobalt and Sm 2 Co 17 were observed in the materials produced after 2 hours at 1100 or 1200 C. (orig.)

cobalt (ii), nickel (ii)

African Journals Online (AJOL)

DR. AMINU

Department of Chemistry Bayero University, P. M. B. 3011, Kano, Nigeria. E-mail: hnuhu2000@yahoo.com. ABSTRACT. The manganese (II), cobalt (II), nickel (II) and .... water and common organic solvents, but are readily soluble in acetone. The molar conductance measurement [Table 3] of the complex compounds in.

Catalytic oxidation of volatile organic compounds (n-hexane, benzene, toluene, o-xylene promoted by cobalt catalysts supported on γ-Al2O3-CeO2

Directory of Open Access Journals (Sweden)

R. Balzer

2014-09-01

Full Text Available Cobalt catalysts supported on γ-alumina, ceria and γ-alumina-ceria, with 10 or 20%wt of cobalt load, prepared by the wet impregnation method and characterized by X-ray diffraction (XRD, scanning electron microscopy (SEM, field emission transmission electron microscopy (FETEM, N2 adsorption-desorption isotherms (BET/BJH methods, energy-dispersive X-ray spectroscopy (EDX, X-ray photoemission spectroscopy (XPS, O2-chemisorption and temperature programmed reduction (TPR were used to promote the oxidation of volatile organic compounds (n-hexane, benzene, toluene and o-xylene. For a range of low temperatures (50-350 °C, the activity of the catalysts with a higher cobalt load (20% wt was greater than that of the catalysts with a lower cobalt load (10% wt. The Co/γ-Al2O3-CeO2 catalytic systems presented the best performances. The results obtained in the characterization suggest that the higher catalytic activity of the Co20/γ-Al2O3-CeO2 catalyst may be attributed to the higher metal content and amount of oxygen vacancies, as well as the effects of the interaction between the cobalt and the alumina and cerium oxides.

Cobalt

Science.gov (United States)

Slack, John F.; Kimball, Bryn E.; Shedd, Kim B.; Schulz, Klaus J.; DeYoung,, John H.; Seal, Robert R.; Bradley, Dwight C.

2017-12-19

Cobalt is a silvery gray metal that has diverse uses based on certain key properties, including ferromagnetism, hardness and wear-resistance when alloyed with other metals, low thermal and electrical conductivity, high melting point, multiple valences, and production of intense blue colors when combined with silica. Cobalt is used mostly in cathodes in rechargeable batteries and in superalloys for turbine engines in jet aircraft. Annual global cobalt consumption was approximately 75,000 metric tons in 2011; China, Japan, and the United States (in order of consumption amount) were the top three cobalt-consuming countries. In 2011, approximately 109,000 metric tons of recoverable cobalt was produced in ores, concentrates, and intermediate products from cobalt, copper, nickel, platinum-group-element (PGE), and zinc operations. The Democratic Republic of the Congo (Congo [Kinshasa]) was the principal source of mined cobalt globally (55 percent). The United States produced a negligible amount of byproduct cobalt as an intermediate product from a PGE mining and refining operation in southeastern Montana; no U.S. production was from mines in which cobalt was the principal commodity. China was the leading refiner of cobalt, and much of its production came from cobalt ores, concentrates, and partially refined materials imported from Congo (Kinshasa).The mineralogy of cobalt deposits is diverse and includes both primary (hypogene) and secondary (supergene) phases. Principal terrestrial (land-based) deposit types, which represent most of world’s cobalt mine production, include primary magmatic Ni-Cu(-Co-PGE) sulfides, primary and secondary stratiform sediment-hosted Cu-Co sulfides and oxides, and secondary Ni-Co laterites. Seven additional terrestrial deposit types are described in this chapter. The total terrestrial cobalt resource (reserves plus other resources) plus past production, where available, is calculated to be 25.5 million metric tons. Additional resources of

The mathematical description of the electrosynthesis of composites of oxy-hydroxycompounds cobalt with polypyrrole overooxidazed

Directory of Open Access Journals (Sweden)

V. V. Tkach

2016-03-01

Full Text Available The electrosynthesis of pereoxidized polypyrrole composite with oxy-hydroxy compounds cobalt in a strongly acidic environment has been described mathematically, using linear stability theory and bifurcation analysis. The conditions of stability of stationary states and self-oscillatory and monotonic instability have been described also. The system behavior was compared with behavior of other systems with pereoxidation, electropolymerization of heterocyclic compounds and electrosynthesis of the oxy-hydroxy compounds cobalt.

Coordination compounds of cobalt (3), chromium (3) and vanadium (3) with s-methylthiosemicarbazone of salicylic aldehyde

Energy Technology Data Exchange (ETDEWEB)

Leovats, V.M.; Gehrbehlehu, N.V.; Tsanich, V.D. (AN Moldavskoj SSR, Kishinev. Inst. Khimii)

1982-04-01

Coordination compounds of trivalent cobalt, chromium and vanadium with S-methylthiosemicarbazone of salicylic aldehyde H/sub 2/L of (Co(HL)/sub 2/)XxnH/sub 2/O (X=Cl, Br, I, NO/sub 3/, ClO/sub 4/), (CoL(NH/sub 3/)/sub 3/)NO/sub 3/, (Co(HL)/sub 2/)/sub 2/(Co(NCS)/sub 4/)x2H/sub 2/O, (CoCl(DH)/sub 2/(H/sub 2/L))xH/sub 2/O, (Cr(HL)/sub 2/)XxnH/sub 2/O (X=Cl, NO/sub 3/), (V(HL)/sub 2/)Clx1/2H/sub 2/O, (M(HL)L)xnH/sub 2/O (M=Co, Cr, V) compositions are synthesized and investigated. It is shown, that H/sub 2/L behaves as a tridentate ligand at the expense of (O, N, N) set of donor atoms. The effective magnetic moment of the compounds is calculated.

and cobalt(III) octahedral monomer complexes: Synthesis and ...

Indian Academy of Sciences (India)

In compound 2 the central cobalt is in +3 oxidation state while `in' compound 2, the nickel ion is in +2 oxidation state. The two complexes are isostructural with octahedral coordination environment exhibiting helical twist topology. They also display strong H-bonding as well as CH- interactions to generate 1D chain.

Thermal Plasma Decomposition Of Nickel And Cobalt Compounds

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Woch M.

2015-06-01

Full Text Available The paper presents the study on manufacturing of nickel and cobalt powders by thermal plasma decomposition of the carbonates of these metals. It was shown the dependence of process parameters and grain size of initial powder on the composition of final product which was ether metal powder, collected in the container as well as the nanopowder with crystallite size of 70 - 90 nm, collected on the inner wall of the reaction chamber. The occurrence of metal oxides in the final products was confirmed and discussed.

Preliminary studies of cobalt complexation in groundwater

International Nuclear Information System (INIS)

Warwick, P.; Shaw, P.; Williams, G.M.; Hooker, P.J.

1988-01-01

A relatively non-invasive method has been used to separate complexed from free cobalt-60 in groundwater, using the weak cationic adsorption properties of Sephadex gels, and a mobile phase of natural groundwater. Results show the kinetics of Co complex formation in groundwater to be slow, and that the equilibrium position is affected by temperature, cobalt concentration and the ionic/organic strength of the groundwater. The addition of DAEA cellulose to the groundwater to remove humic material, also removed the majority of organic species which absorb UV at 254 nm, but 45% of the original total organic carbon remained, and the amount of complexed cobalt left in solution was only reduced to 76% of its former concentration. This suggests that the completed Co species separated by the method described in this paper are a mixture of inorganic and organic compounds, and studies are therefore continuing to establish their exact nature. (author)

Preliminary studies of cobalt complexation in groundwater

International Nuclear Information System (INIS)

Warwick, P.; Shaw, P.; Williams, G.M.; Hooker, P.J.

1988-01-01

A relatively non-invasive method has been used to separate complexed from free cobalt-60 in groundwater, using the weak cationic adsorption properties of Sephadex gels, and a mobile phase of natural groundwater. Results show the kinetics of Co complex formation in groundwater to be slow, and that the equilibrium position is affected by temperature, cobalt concentration and the ionic/organic strength of the groundwater. The addition of DEAE cellulose to the groundwater to remove humic material, also removed the majority of organic species with absorb UV at 254 nm, but 45% of the original total organic carbon remained, and the amount of complexed cobalt left in solution was only reduced to 76% of its former concentration. This suggests that the complexed Co species separated by the method described in this paper are a mixture of inorganic and organic compounds, and studies are therefore continuing to establish their exact nature. (orig.)

Synthesis and structures of two cobalt compounds of 2-amino-2 ...

Indian Academy of Sciences (India)

as catalysis, magnetism and luminescence.1 7 One of the most fascinating challenges ... program and refined by the full-matrix least-squares method on F2 with the ..... R E P 2012 Synthesis and characterisation of cobalt(II) phosphonate cage ...

A new three-dimensional cobalt phosphate: Co5(OH2)4(HPO4)2(PO4)2

International Nuclear Information System (INIS)

Han Zhangang; Tian Aixiang; Peng Jun; Zhai Xueliang

2006-01-01

A three-dimensional (3D) cobalt phosphate: Co 5 (OH 2 ) 4 (HPO 4 ) 2 (PO 4 ) 2 (1), has been synthesized by hydrothermal reaction and characterized by single-crystal X-ray diffraction, thermogravimetric analysis, and magnetic techniques. The title compound is a template free cobalt phosphate. Compound 1 exhibits a complex net architecture based on edge- and corner-sharing of CoO 6 and PO 4 polyhedra. The magnetic susceptibility measurements indicated that the title compound obeys Curie-Weiss behavior down to a temperature of 17 K at which an antiferromagnetic phase transition occurs. - Graphical abstract: A 3D cobalt phosphate with a neutral framework: Co 5 (OH 2 ) 4 (HPO 4 ) 2 (PO 4 ) 2 (1), has been synthesized and characterized. Compound 1 exhibits a complex net architecture based on edge- and corner-sharing of CoO 6 and PO 4 polyhedra. Its magnetic property was researched

Comparative effects of cobalt, nickel and copper on plant growth

Energy Technology Data Exchange (ETDEWEB)

Brenchley, W E

1938-11-01

An account is given of the present position of our knowledge with regard to the distribution and the physiological importance of nickel and cobalt, in relation to plants and animals. Experiments on barley and broad beans were carried out in water cultures with the sulfates and chlorides of cobalt, nickel and copper. In every case a range of low concentrations did little or no damage, but toxic action occurred abruptly above a concentration which varied with the species and with the compound. With barley, copper was the most poisonous element in either compound, but the differences were not striking. Low concentrations of the sulfate were innocuous, but parallel low strengths of the chloride caused a slight, significant depression in growth. With broad beans, cobalt was much more poisonous than either nickel or copper, particularly with the sulfate. No slight depression with low concentrations of the chloride was noticeable with this species. The morphological response to toxicity varied with the element concerned. Copper, in poisonous strengths, caused shortening and bunching of barley roots, whereas nickel and cobalt permitted the growth of elongated roots of a very attenuated nature. The individuality of plant response to poison was frequently shown by the great variation in growth in the borderline concentrations just below those which caused marked depression of growth.

A new three-dimensional cobalt phosphate: Co 5(OH 2) 4(HPO 4) 2(PO 4) 2

Science.gov (United States)

Han, Zhangang; Tian, Aixiang; Peng, Jun; Zhai, Xueliang

2006-10-01

A three-dimensional (3D) cobalt phosphate: Co 5(OH 2) 4(HPO 4) 2(PO 4) 2 ( 1), has been synthesized by hydrothermal reaction and characterized by single-crystal X-ray diffraction, thermogravimetric analysis, and magnetic techniques. The title compound is a template free cobalt phosphate. Compound 1 exhibits a complex net architecture based on edge- and corner-sharing of CoO 6 and PO 4 polyhedra. The magnetic susceptibility measurements indicated that the title compound obeys Curie-Weiss behavior down to a temperature of 17 K at which an antiferromagnetic phase transition occurs.

Mechanism of caesium ion exchange on potassium cobalt hexacyanoferrates(II)

Energy Technology Data Exchange (ETDEWEB)

Lehto, J.; Haukka, S.; Harjula, R. (Helsinki Univ. (Finland). Dept. of Radiochemistry); Blomberg, M. (Helsinki Univ. (Finland). Dept. of Physics)

1990-03-01

The caesium uptakes by K{sub 2}(CoFe(CN){sub 6}) and non-stoicheiometric compounds K{sub 2/x}Co{sub x/2}(CoFe(CN){sub 6}) were found to correlate directly with the specific surface areas of the products with x < 1. The exchange process is assumed to involve only the outermost surface layer of their crystals, which have cubic lattice, i.e. only potassium (or cobalt) ions inside the elementary cubes closest to the surface of the crystals are exchanged for caesium ions. Compounds with x > 1 are mixtures of cubic potassium cobalt hexacyanoferrate (ii) and tetragonal Co{sub 2}Fe(CN){sub 6}. The thermodynamic equilibrium constant of the caesium exchange on K{sub 2}(CoFe(CN){sub 6}) was found to have a high value of 125. (author).

An Efficient and Recyclable Nanoparticle-Supported Cobalt Catalyst for Quinoxaline Synthesis

Directory of Open Access Journals (Sweden)

Fatemeh Rajabi

2015-11-01

Full Text Available The syntheses of quinoxalines derived from 1,2-diamine and 1,2-dicarbonyl compounds under mild reaction conditions was carried out using a nanoparticle-supported cobalt catalyst. The supported nanocatalyst exhibited excellent activity and stability and it could be reused for at least ten times without any loss of activity. No cobalt contamination could be detected in the products by AAS measurements, pointing to the excellent activity and stability of the Co nanomaterial.

Recovery of Cobalt as Cobalt Oxalate from Cobalt Tailings Using Moderately Thermophilic Bioleaching Technology and Selective Sequential Extraction

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Guobao Chen

2016-07-01

Full Text Available Cobalt is a very important metal which is widely applied in various critical areas, however, it is difficult to recover cobalt from minerals since there is a lack of independent cobalt deposits in nature. This work is to provide a complete process to recover cobalt from cobalt tailings using the moderately thermophilic bioleaching technology and selective sequential extraction. It is found that 96.51% Co and 26.32% Cu were extracted after bioleaching for four days at 10% pulp density. The mean compositions of the leach solutions contain 0.98 g·L−1 of Co, 6.52 g·L−1 of Cu, and 24.57 g·L−1 of Fe (III. The copper ion was then recovered by a solvent extraction process and the ferric ions were selectively removed by applying a goethite deironization process. The technological conditions of the above purification procedures were deliberately discussed. Over 98.6% of copper and 99.9% of ferric ions were eliminated from the leaching liquor. Cobalt was finally produced as cobalt oxalate and its overall recovery during the whole process was greater than 95%. The present bioleaching process of cobalt is worth using for reference to deal with low-grade cobalt ores.

Polytypic transformations during the thermal decomposition of cobalt hydroxide and cobalt hydroxynitrate

International Nuclear Information System (INIS)

Ramesh, Thimmasandra Narayan

2010-01-01

The isothermal decomposition of cobalt hydroxide and cobalt hydroxynitrate at different intervals of temperature leads to the formation of Co 3 O 4 . The phase evolution during the decomposition process was monitored using powder X-ray diffraction. The transformation of cobalt hydroxide to cobalt oxide occurs via three phase mixture while cobalt hydroxynitrate to cobalt oxide occurs through a two phase mixture. The nature of the sample and its preparation method controls the decomposition mechanism. The comparison of topotactical relationship between the precursors to the decomposed product has been reported in relation to polytypism. - Graphical abstract: Isothermal thermal decomposition studies of cobalt hydroxide and cobalt hydroxynitrate at different intervals of temperature show the metastable phase formed prior to Co 3 O 4 phase.

Half-sandwich cobalt complexes in the metal-organic chemical vapor deposition process

Energy Technology Data Exchange (ETDEWEB)

Georgi, Colin [Technische Universität Chemnitz, Faculty of Natural Science, Institute of Chemistry, Inorganic Chemistry, Chemnitz 09107 (Germany); Hapke, Marko; Thiel, Indre [Leibniz-Institut für Katalyse e.V. an der Universität Rostock (LIKAT), Albert-Einstein-Straße 29a, Rostock 18059 (Germany); Hildebrandt, Alexander [Technische Universität Chemnitz, Faculty of Natural Science, Institute of Chemistry, Inorganic Chemistry, Chemnitz 09107 (Germany); Waechtler, Thomas; Schulz, Stefan E. [Fraunhofer Institute of Electronic Nano Systems (ENAS), Technologie-Campus 3, Chemnitz 09126 (Germany); Technische Universität Chemnitz, Center for Microtechnologies (ZfM), Chemnitz 09107 (Germany); Lang, Heinrich, E-mail: heinrich.lang@chemie.tu-chemnitz.de [Technische Universität Chemnitz, Faculty of Natural Science, Institute of Chemistry, Inorganic Chemistry, Chemnitz 09107 (Germany)

2015-03-02

A series of cobalt half-sandwich complexes of type [Co(η{sup 5}-C{sub 5}H{sub 5})(L)(L′)] (1: L, L′ = 1,5-hexadiene; 2: L = P(OEt){sub 3}, L′ = H{sub 2}C=CHSiMe{sub 3}; 3: L = L′ = P(OEt){sub 3}) has been studied regarding their physical properties such as the vapor pressure, decomposition temperature and applicability within the metal-organic chemical vapor deposition (MOCVD) process, with a focus of the influence of the phosphite ligands. It could be shown that an increasing number of P(OEt){sub 3} ligands increases the vapor pressure and thermal stability of the respective organometallic compound. Complex 3 appeared to be a promising MOCVD precursor with a high vapor pressure and hence was deposited onto Si/SiO{sub 2} (100 nm) substrates. The resulting reflective layer is closed, dense and homogeneous, with a slightly granulated surface morphology. X-ray photoelectron spectroscopy (XPS) studies demonstrated the formation of metallic cobalt, cobalt phosphate, cobalt oxide and cobalt carbide. - Highlights: • Thermal studies and vapor pressure measurements of cobalt half-sandwich complexes was carried out. • Chemical vapor deposition with cobalt half-sandwich complexes is reported. • The use of Co-phosphites results in significant phosphorous-doped metallic layers.

The effect of organics on the sorption of cobalt by glacial sand in laboratory experiments

International Nuclear Information System (INIS)

Haigh, G.; Williams, G.M.; Hooker, P.J.; Ross, C.A.M.; Allen, M.R.

1989-02-01

The effect of acetate, EDTA and natural organic compounds in groundwater at Drigg test site, on the sorption of cobalt by glacial sand has been studied in a series of batch experiments. Removing 50% of the organic material from the groundwater with DEAE cellulose increased the distribution ratio (R d ) of cobalt by a factor of about two. The addition of both EDTA and acetate to the sand/water system led to the removal of Ca, Mg, Sr and Ba from solution. Both organic compounds had the effect of reducing the pH and bicarbonated concentrations. EDTA also removed iron from the solution. EDTA reduced the R d for Co by up to 2 orders of magnitude. At EDTA concentrations greater than 5mg/1, there was no further reduction in sorption. EDTA was not itself sorbed, but formed a mobile complex with Co. Within the same period of equilibrium, the R d values were lower when EDTA was allowed to equilibrate with the sand before adding cobalt. The desorption of cobalt from the minerals surface may be a rate limiting step such that equilibrium was not achieved within the 14 day period of these experiments. Acetate had no effect of cobalt sorption. (author)

Blood doping by cobalt. Should we measure cobalt in athletes?

Directory of Open Access Journals (Sweden)

Guidi Gian

2006-07-01

Full Text Available Abstract Background Blood doping is commonplace in competitive athletes who seek to enhance their aerobic performances through illicit techniques. Presentation of the hypothesis Cobalt, a naturally-occurring element with properties similar to those of iron and nickel, induces a marked and stable polycythemic response through a more efficient transcription of the erythropoietin gene. Testing the hypothesis Although little information is available so far on cobalt metabolism, reference value ranges or supplementation in athletes, there is emerging evidence that cobalt is used as a supplement and increased serum concentrations are occasionally observed in athletes. Therefore, given the athlete's connatural inclination to experiment with innovative, unfair and potentially unhealthy doping techniques, cobalt administration might soon become the most suited complement or surrogate for erythropoiesis-stimulating substances. Nevertheless, cobalt administration is not free from unsafe consequences, which involve toxic effects on heart, liver, kidney, thyroid and cancer promotion. Implications of the hypothesis Cobalt is easily purchasable, inexpensive and not currently comprehended within the World Anti-Doping Agency prohibited list. Moreover, available techniques for measuring whole blood, serum, plasma or urinary cobalt involve analytic approaches which are currently not practical for antidoping laboratories. Thus more research on cobalt metabolism in athletes is compelling, along with implementation of effective strategies to unmask this potentially deleterious doping practice

Cobalt Cardiomyopathy Secondary to Hip Arthroplasty: An Increasingly Prevalent Problem

Directory of Open Access Journals (Sweden)

Russel Tilney

2017-01-01

Full Text Available A forty-year-old man experienced worsening heart failure four years following bilateral complicated total hip replacement. His condition was extensively worked up but no underlying pathology was immediately evident. Given the cobalt-chromium alloy component present in the hip arthroplasties, the raised cobalt blood levels, and a fitting clinical picture coupled with radiological findings, the patient underwent right hip revision. Evidence of biotribocorrosion was present on direct visualisation intraoperatively. The patient subsequently experienced symptomatic improvement (NYHA class III to class I and echocardiography showed recovery of ejection fraction. Cobalt exists as a bivalent and trivalent molecule in circulation and produces a cytotoxicity profile similar to nanoparticles, causing neurological, thyroid, and cardiological pathology. Blood levels are not entirely useful as there is no identifiable conversion factor for levels in whole blood, serum, and erythrocytes which seem to act independently of each other. Interestingly cobalt cardiomyopathy is frequently compounded by other possible causes of cardiomyopathy such as alcohol and a link has been postulated. Definitive treatment is revision of the arthroplasty as other treatments are unproven.

Cobalt release from inexpensive jewellery

DEFF Research Database (Denmark)

Thyssen, Jacob Pontoppidan; Jellesen, Morten Stendahl; Menné, Torkil

2010-01-01

. Conclusions: This study showed that only a minority of inexpensive jewellery purchased in Denmark released cobalt when analysed with the cobalt spot test. As fashion trends fluctuate and we found cobalt release from dark appearing jewellery, cobalt release from consumer items should be monitored in the future......Objectives: The aim was to study 354 consumer items using the cobalt spot test. Cobalt release was assessed to obtain a risk estimate of cobalt allergy and dermatitis in consumers who would wear the jewellery. Methods: The cobalt spot test was used to assess cobalt release from all items...

Cobalt toxicity: Chemical and radiological combined effects on HaCaT keratinocyte cell line

International Nuclear Information System (INIS)

Sandre, C.; Moulin, C.; Bresson, C.; Gault, N.; Poncy, J. L.; Lefaix, J. L.

2010-01-01

Cobalt (Co) is an essential trace element well known as a constituent of vitamin B 12 , but different compounds of Co are also described as highly toxic and/or radio-toxic for individuals or the environment. In nuclear power plants, 58 Co and 60 Co are radioactive isotopes of cobalt present as activation products of stable Co and Ni used in alloys. Skin exposure is a current occupational risk in the hard metal and nuclear industries. As biochemical and molecular cobalt-induced toxicological mechanisms are not fully identified, we investigated cobalt toxicity in a model human keratinocyte cell line, HaCaT. In this study, we propose a model to determine the in vitro chemical impact on cell viability of a soluble form of cobalt (CoCl 2 ) with or without gamma-ray doses to mimic contamination by 60 Co, to elucidate the mechanisms of cobalt intracellular chemical and radiological toxicity. Intracellular cobalt concentration was determined after HaCaT cell contamination and chemical toxicity was evaluated in terms of cellular viability and clonogenic survival. We investigated damage to DNA in HaCaT cells by combined treatment with chemical cobalt and a moderate gamma-ray dose. Additive effects of cobalt and irradiation were demonstrated. The underlying mechanism of cobalt toxicity is not clearly established, but our results seem to indicate that the toxicity of Co(II) and of irradiation arises from production of reactive oxygen species. (authors)

Cobalt toxicity: Chemical and radiological combined effects on HaCaT keratinocyte cell line

Energy Technology Data Exchange (ETDEWEB)

Gault, N. [CEA Fontenay aux Roses, DSV/IRCM/SCSR/LRTS, 92265 Fontenay aux Rose (France); Sandre, C.; Moulin, B.; Bresson, C. [CEA, DEN, SECR, Laboratoire de Speciation des Radionucleides et des Molecules, F-91191 Gif-sur-Yvette (France); Poncy, J.L. [CEA Bruyeres Le Chatel, DSV/IRCM/SREIT/LRT, 91680 Bruyeres Le Chatel (France); Lefaix, J.L. [CEA Caen, DSV/IRCM/SRO/LARIA, 14070 Caen (France)

2010-07-01

Cobalt (Co) is an essential trace element well known as a constituent of vitamin B12, but different compounds of Co are also described as highly toxic and/or radio-toxic for individuals or the environment. In nuclear power plants, {sup 58}Co and {sup 60}Co are radioactive isotopes of cobalt present as activation products of stable Co and Ni used in alloys. Skin exposure is a current occupational risk in the hard metal and nuclear industries. As biochemical and molecular cobalt-induced toxicological mechanisms are not fully identified, we investigated cobalt toxicity in a model human keratinocyte cell line, HaCaT. In this study, we propose a model to determine the in vitro chemical impact on cell viability of a soluble form of cobalt (CoCl{sub 2}) with or without {gamma}-ray doses to mimic contamination by {sup 60}Co, to elucidate the mechanisms of cobalt intracellular chemical and radiological toxicity. Intracellular cobalt concentration was determined after HaCaT cell contamination and chemical toxicity was evaluated in terms of cellular viability and clonogenic survival. We investigated damage to DNA in HaCaT cells by combined treatment with chemical cobalt and a moderate {gamma}-ray dose. Additive effects of cobalt and irradiation were demonstrated. The underlying mechanism of cobalt toxicity is not clearly established, but our results seem to indicate that the toxicity of Co(II) and of irradiation arises from production of reactive oxygen species. (authors)

Cobalt toxicity: Chemical and radiological combined effects on HaCaT keratinocyte cell line

Energy Technology Data Exchange (ETDEWEB)

Sandre, C.; Moulin, C.; Bresson, C. [CEA Saclay, DEN, SECR, Lab Speciat Radionucleides and Mol, F-91191 Gif Sur Yvette (France); Gault, N. [CEA Fontenay Roses, DSV IRCM SCSR LRTS, F-92265 Fontenay Aux Roses (France); Poncy, J. L. [CEA Bruyeres Le Chatel, DSV IRCM SREIT LRT, F-91680 Bruyeres Le Chatel (France); Lefaix, J. L. [CEA Caen, DSV IRCM SRO LARIA, F-14070 Caen (France)

2010-07-01

Cobalt (Co) is an essential trace element well known as a constituent of vitamin B{sub 12}, but different compounds of Co are also described as highly toxic and/or radio-toxic for individuals or the environment. In nuclear power plants, {sup 58}Co and {sup 60}Co are radioactive isotopes of cobalt present as activation products of stable Co and Ni used in alloys. Skin exposure is a current occupational risk in the hard metal and nuclear industries. As biochemical and molecular cobalt-induced toxicological mechanisms are not fully identified, we investigated cobalt toxicity in a model human keratinocyte cell line, HaCaT. In this study, we propose a model to determine the in vitro chemical impact on cell viability of a soluble form of cobalt (CoCl{sub 2}) with or without gamma-ray doses to mimic contamination by {sup 60}Co, to elucidate the mechanisms of cobalt intracellular chemical and radiological toxicity. Intracellular cobalt concentration was determined after HaCaT cell contamination and chemical toxicity was evaluated in terms of cellular viability and clonogenic survival. We investigated damage to DNA in HaCaT cells by combined treatment with chemical cobalt and a moderate gamma-ray dose. Additive effects of cobalt and irradiation were demonstrated. The underlying mechanism of cobalt toxicity is not clearly established, but our results seem to indicate that the toxicity of Co(II) and of irradiation arises from production of reactive oxygen species. (authors)

Cobalt release from inexpensive jewellery: has the use of cobalt replaced nickel following regulatory intervention?

Science.gov (United States)

Thyssen, Jacob Pontoppidan; Jellesen, Morten S; Menné, Torkil; Lidén, Carola; Julander, Anneli; Møller, Per; Johansen, Jeanne Duus

2010-08-01

Before the introduction of the EU Nickel Directive, concern was raised that manufacturers of jewellery might turn from the use of nickel to cobalt following the regulatory intervention on nickel exposure. The aim was to study 354 consumer items using the cobalt spot test. Cobalt release was assessed to obtain a risk estimate of cobalt allergy and dermatitis in consumers who would wear the jewellery. The cobalt spot test was used to assess cobalt release from all items. Microstructural characterization was made using scanning electron microscope (SEM) and energy-dispersive spectroscopy (EDS). Cobalt release was found in 4 (1.1%) of 354 items. All these had a dark appearance. SEM/EDS was performed on the four dark appearing items which showed tin-cobalt plating on these. This study showed that only a minority of inexpensive jewellery purchased in Denmark released cobalt when analysed with the cobalt spot test. As fashion trends fluctuate and we found cobalt release from dark appearing jewellery, cobalt release from consumer items should be monitored in the future. Industries may not be fully aware of the potential cobalt allergy problem.

Cobalt

International Nuclear Information System (INIS)

Stolyarova, I.A.; Bunakova, N.Yu.

1983-01-01

The neutron-activation method for determining cobalt in rocks, polymetallic and iron ores and rockforming minerals at 2x10 -6 -5x10 -3 % content is developed. Cobalt determination is based on the formation under the effect of thermal neutrons of nuclear reactor of the 60 Co radioactive isotope by the 59 Co (n, γ) 60 Co reaction with radiation energy of the most intensive line of 1333 keV. Cobalt can be determined by the scheme of the multicomponent analysis from the sample with other elements. Co is determined in the solution after separation of all determinable by the scheme elements. The 60 Co intensity is measured by the mUltichannel gamma-spectrometer with Ge(Li)-detector

Cobalt release from implants and consumer items and characteristics of cobalt sensitized patients with dermatitis

DEFF Research Database (Denmark)

Thyssen, Jacob Pontoppidan; Menne, Torkil; Liden, Carola

2012-01-01

-containing dental alloys and revised hip implant components.Results. Six of eight dental alloys and 10 of 98 revised hip implant components released cobalt in the cobalt spot test, whereas none of 50 mobile phones gave positive reactions. The clinical relevance of positive cobalt test reactions was difficult......-tested dermatitis patients in an attempt to better understand cobalt allergy.Materials and methods. 19 780 dermatitis patients aged 4-99 years were patch tested with nickel, chromium or cobalt between 1985 and 2010. The cobalt spot test was used to test for cobalt ion release from mobile phones as well as cobalt...

Cobalt chloride speciation, mechanisms of cytotoxicity on human pulmonary cells, and synergistic toxicity with zinc

International Nuclear Information System (INIS)

Bresson, Carole; Darolles, Carine; Sage, Nicole; Malard, Veronique; Carmona, Asuncion; Roudeau, Stephane; Ortega, Richard; Gautier, Celine; Ansoborlo, Eric

2013-01-01

Cobalt is used in numerous industrial sectors, leading to occupational diseases, particularly by inhalation. Cobalt-associated mechanisms of toxicity are far from being understood and information that could improve knowledge in this area is required. We investigated the impact of a soluble cobalt compound, CoCl 2 .6H 2 O, on the BEAS-2B lung epithelial cell line, as well as its impact on metal homeostasis. Cobalt speciation in different culture media, in particular soluble and precipitated cobalt species, was investigated via theoretical and analytical approaches. The cytotoxic effects of cobalt on the cells were assessed. Upon exposure of BEAS-2B cells to cobalt, intracellular accumulation of cobalt and zinc was demonstrated using direct in situ microchemical analysis based on ion micro-beam techniques and analysis after cell lysis by inductively coupled plasma mass spectrometry (ICP-MS). Microchemical imaging revealed that cobalt was rather homogeneously distributed in the nucleus and in the cytoplasm whereas zinc was more abundant in the nucleus. The modulation of zinc homeostasis led to the evaluation of the effect of combined cobalt and zinc exposure. In this case, a clear synergistic increase in toxicity was observed as well as a substantial increase in zinc content within cells. Western blots performed under the same co-exposure conditions revealed a decrease in ZnT1 expression, suggesting that cobalt could inhibit zinc release through the modulation of ZnT1. Overall, this study highlights the potential hazard to lung function, of combined exposure to cobalt and zinc. (authors)

Cobalt chloride speciation, mechanisms of cytotoxicity on human pulmonary cells, and synergistic toxicity with zinc

International Nuclear Information System (INIS)

Bresson, Carole; Darolles, Carine; Sage, Nicole; Malard, Veronique; Carmona, Asuncion; Roudeau, Stephane; Ortega, Richard; Gautier, Celine; Ansoborlo, Eric

2013-01-01

Complete text of publication follows: Cobalt is used in numerous industrial sectors, leading to occupational diseases, particularly by inhalation. Cobalt-associated mechanisms of toxicity are far from being understood and information that could improve knowledge in this area is required. We investigated the impact of a soluble cobalt compound, CoCl 2 , on the BEAS-2B lung epithelial cell line, as well as its impact on metal homeostasis. Cobalt speciation in different culture media, in particular soluble and precipitated cobalt species, was investigated via theoretical and analytical approaches. The cytotoxic effects of cobalt on the cells were assessed. Upon exposure of BEAS-2B cells to cobalt, intracellular accumulation of cobalt and zinc was demonstrated using direct in situ microchemical analysis based on ion micro-beam techniques and analysis after cell lysis by inductively coupled plasma mass spectrometry (ICP-MS). Microchemical imaging revealed that cobalt was rather homogeneously distributed in the nucleus and in the cytoplasm whereas zinc was more abundant in the nucleus. The modulation of zinc homeostasis led to the evaluation of the effect of combined cobalt and zinc exposure. In this case, a clear synergistic increase in toxicity was observed as well as a substantial increase in zinc content within cells. Western blots performed under the same co-exposure conditions revealed a decrease in ZnT1 expression, suggesting that cobalt could inhibit zinc release through the modulation of ZnT1. Overall, this study highlights the potential hazard to lung function, of combined exposure to cobalt and zinc

Speciation of cobalt-chloride-based ionic liquids and electrodeposition of Co wires

International Nuclear Information System (INIS)

Hsieh, Yi-Ting; Lai, Mei-Chun; Huang, Hsin-Liang; Sun, I.-Wen

2014-01-01

Highlights: • Template-free electrodeposition of cobalt nanowires arrays can be achieved from Lewis acidic CoCl 2 -EMIC ionic liquids. • SEM and TEM images reveal the diameter of the nanowire is around 200 nm, and the XPS data shows that cobalt oxide is formed at the surface of the nanowire. • MALDI-TOF-MS, XAS, and UV-vis spectroscopy results show that the coordination number and the mean Co-Cl bond length are depending on the molar ratio of CoCl 2 and EMIC. - Abstract: The speciation and coordination of cobalt-chloride-based ionic liquids with various mole percentages of CoCl 2 were investigated using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS), X-ray absorption spectroscopy (XAS), ultraviolet-visible absorption spectroscopy, and cyclic voltammetry. The coordination number and the mean Co-Cl bond length decreases with increasing CoCl 2 concentration, indicating that various Co(II) chloride compounds such as CoCl 4 2- , Co 2 Cl 5 - , and Co 3 Cl 7 − are formed depending on the molar ratio of CoCl 2 and EMIC in the melt. While the [CoCl 4 ] 2− complex formed in the Lewis basic melts and is electrochemically inactive within the electrochemical window of the melt, the other coordination-unsaturated cobalt chloride compounds formed in Lewis acidic melts can be electrochemically reduced to cobalt metal. The template-free electrodeposition of Co nanowires can be achieved from 40-60 mol% and 50-50 mol% CoCl 2 -EMIC (1-ethyl-3-methylimidazolium chloride) ionic liquids without any additives. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS) were used to characterize the surface of the deposits

A spin-frustrated cobalt(II) carbonate pyrochlore network.

Science.gov (United States)

Zheng, Yanzhen; Ellern, Arkady; Kögerler, Paul

2011-11-01

The crystal structure of the cobalt(II) carbonate-based compound cobalt(II) dicarbonate trisodium chloride, Co(CO(3))(2)Na(3)Cl, grown from a water-ethanol mixture, exhibits a three-dimensional network of corner-sharing {Co(4)(μ(3)-CO(3))(4)} tetrahedral building blocks, in which the Co(II) centres define a pyrochlore lattice and reside in a slightly distorted octahedral Co(O-CO(2))(6) environment. The space outside the hexagonal framework defined by these interlinked groups is occupied by Na(+) and Cl(-) ions. Antiferromagnetic coupling between adjacent Co(II) centres, mediated by carbonate bridges, results in geometric spin frustration which is typical for pyrochlore networks. The Co and Cl atoms reside on the special position 3, one Na atom on position 2 and a carbonate C atom on position 3.

Co-exposure to nickel and cobalt chloride enhances cytotoxicity and oxidative stress in human lung epithelial cells.

Science.gov (United States)

Patel, Eshan; Lynch, Christine; Ruff, Victoria; Reynolds, Mindy

2012-02-01

Nickel and cobalt are heavy metals found in land, water, and air that can enter the body primarily through the respiratory tract and accumulate to toxic levels. Nickel compounds are known to be carcinogenic to humans and animals, while cobalt compounds produce tumors in animals and are probably carcinogenic to humans. People working in industrial and manufacturing settings have an increased risk of exposure to these metals. The cytotoxicity of nickel and cobalt has individually been demonstrated; however, the underlying mechanisms of co-exposure to these heavy metals have not been explored. In this study, we investigated the effect of exposure of H460 human lung epithelial cells to nickel and cobalt, both alone and in combination, on cell survival, apoptotic mechanisms, and the generation of reactive oxygen species and double strand breaks. For simultaneous exposure, cells were exposed to a constant dose of 150 μM cobalt or nickel, which was found to be relatively nontoxic in single exposure experiments. We demonstrated that cells exposed simultaneously to cobalt and nickel exhibit a dose-dependent decrease in survival compared to the cells exposed to a single metal. The decrease in survival was the result of enhanced caspase 3 and 7 activation and cleavage of poly (ADP-ribose) polymerase. Co-exposure increased the production of ROS and the formation of double strand breaks. Pretreatment with N-acetyl cysteine alleviated the toxic responses. Collectively, this study demonstrates that co-exposure to cobalt and nickel is significantly more toxic than single exposure and that toxicity is related to the formation of ROS and DSB. Copyright © 2011 Elsevier Inc. All rights reserved.

THE COORDINATION COMPOUNDS OF COBALT (II, III) WITH DITHIOCARBAMIC ACID DERIVATIVES — MODIFICATORS OF HYDROLYTIC ENZYMES ACTIVITY

OpenAIRE

L. D. Varbanets; О. V. Matselyukh; N. А. Nidyalkova; Е. V. Аvdiyuk; А. V. Gudzenko; I. I. Seifullina; G. N. Маsаnоvets; N. V. Khitrich

2013-01-01

Chloride, bromide and isothiocyanate complexes of cobalt(II) with N-substituted thiocarbamoyl-N?-pentamethylenesulfenamides (1)–(12), and also complexes of cobalt(II, Ш) with derivatives of morpholine-4-carbodithioic acid (13)–(18) have been used as modificators of enzymes of hydrolytic action — Bacillus thurin-giensis ІМВ В-7324 peptidases, Bacillus subtilis 147 and Aspergillus flavus var. oryzae 80428 amylases, Eupenicillium erubescens 248 and Cryptococcus albidus 1001 rhamnosidases. It was...

Preparation of Fischer-Tropsch catalysts from cobalt/iron hydrotalcites

Energy Technology Data Exchange (ETDEWEB)

Howard, B.H.; Boff, J.J.; Zarochak, M.F. [Pittsburgh Energy Technology Center, PA (United States)] [and others

1995-12-31

Compounds with the (hydrotalcites) have properties that make them attractive as precursors for Fischer-Tropsch catalysts. A series of single-phase hydrotalcites with cobalt/iron atom ratios ranging from 75/25 to 25/75 has been synthesized. Mixed cobalt/iron oxides have been prepared from these hydrotalcites by controlled thermal decomposition. Thermal decomposition at temperatures below 600 {degrees}C typically produced a single-phase mixed metal oxide with a spinel structure. The BET surface areas of the spinal samples have been found to be as high as about 150 m{sup 2}/g. Appropriate reducing pretreatments have been developed for several of these spinels and their activity, selectivity, and activity and selectivity maintenance have been examined at 13 MPa in a fixed-bed microreactor.

Cobalt doped CuMnOx catalysts for the preferential oxidation of carbon monoxide

Science.gov (United States)

Dey, Subhashish; Dhal, Ganesh Chandra; Mohan, Devendra; Prasad, Ram; Gupta, Rajeev Nayan

2018-05-01

Carbon monoxide (CO) is a poisonous gas, recognized as a silent killer for the 21st century. It is produced from the partial oxidation of carbon containing compounds. The catalytic oxidation of CO receives a huge attention due to its applications in different fields. In the present work, hopcalite (CuMnOx) catalysts were synthesized using a co-precipitation method for CO oxidation purposes. Also, it was doped with the cobalt by varying concentration from 1 to 5wt%. It was observed that the addition of cobalt into the CuMnOx catalyst (by the deposition-precipitation method) improved the catalytic performance for the low-temperature CO oxidation. CuMnOx catalyst doped with 3wt% of cobalt exhibited most active performance and showed the highest activity than other cobalt concentrations. Different analytical tools (i.e. XRD, FTIR, BET, XPS and SEM-EDX) were used to characterize the as-synthesized catalysts. It was expected that the introduction of cobalt will introduce new active sites into the CuMnOx catalyst that are associated with the cobalt nano-particles. The order of calcination strategies based on the activity for cobalt doped CuMnOx catalysts was observed as: Reactive calcinations (RC) > flowing air > stagnant air. Therefore, RC (4.5% CO in air) route can be recommended for the synthesis of highly active catalysts. The catalytic activity of doped CuMnOx catalysts toward CO oxidation shows a correlation among average oxidation number of Mn and the position and the nature of the doped cobalt cation.

Passivation and corrosion behaviours of cobalt and cobalt-chromium-molybdenum alloy

International Nuclear Information System (INIS)

Metikos-Hukovic, M.; Babic, R.

2007-01-01

Passivation and corrosion behaviour of the cobalt and cobalt-base alloy Co30Cr6Mo was studied in a simulated physiological solution containing chloride and bicarbonate ions and with pH of 6.8. The oxido-reduction processes included solid state transformations occurring at the cobalt/electrolyte interface are interpreted using theories of surface electrochemistry. The dissolution of cobalt is significantly suppressed by alloying it with chromium and molybdenum, since the alloy exhibited 'chromium like' passivity. The structural and protective properties of passive oxide films formed spontaneously at the open circuit potential or during the anodic polarization were studied using electrochemical impedance spectroscopy in the wide frequency range

HAEM SYNTHASE AND COBALT PORPHYRIN SYNTHASE IN VARIOUS MICRO-ORGANISMS.

Science.gov (United States)

PORRA, R J; ROSS, B D

1965-03-01

1. The preparation of a crude extract of Clostridium tetanomorphum containing cobalt porphyrin synthase but little haem-synthase activity is described. 2. The properties of cobalt porphyrin synthase in the clostridial extracts is compared with the properties of a haem synthase present in crude extracts of the yeast Torulopsis utilis. 3. Cobalt porphyrin synthase in extracts of C. tetanomorphum inserts Co(2+) ions into the following dicarboxylic porphyrins in descending order of rate of insertion: meso-, deutero- and proto-porphyrins. Esterification renders meso- and deutero-porphyrins inactive as substrates. Neither the tetracarboxylic (coproporphyrin III) nor the octacarboxylic (uroporphyrin III) compounds are converted into cobalt porphyrins by the extract, but the non-enzymic incorporation of Co(2+) ions into these two porphyrins is rapid. These extracts are unable to insert Mn(2+), Zn(2+), Mg(2+) or Cu(2+) ions into mesoporphyrin. 4. Crude extracts of T. utilis readily insert both Co(2+) and Fe(2+) ions into deutero-, meso, and proto-porphyrins. Unlike the extracts of C. tetanomorphum, these preparations catalyse the insertion of Co(2+) ions into deuteroporphyrin more rapidly than into mesoporphyrin. This parallels the formation of haems by the T. utilis extract. 5. Cobalt porphyrin synthase is present in the particulate fraction of the extracts of C. tetanomorphum but requires a heat-stable factor present in the soluble fraction. This soluble factor can be replaced by GSH. 6. Cobalt porphyrin synthase in the clostridial extract is inhibited by iodoacetamide and to a smaller extent by p-chloromercuribenzoate and N-ethylmaleimide. The haem synthases of T. utilis and Micrococcus denitrificans are also inhibited by various thiol reagents.

Structural information on the coordination compounds formed by manganese(II), cobalt(II), nickel(II), zinc(II), cadmium(II) and mercury(II) thiocyanates with 4-cyanopyridine N-oxide from their magnetic moments, electronic and infrared spectra

Science.gov (United States)

Ahuja, I. S.; Yadava, C. L.; Singh, Raghuvir

1982-05-01

Coordination compounds formed by the interaction of 4-cyanopyridine. N-oxide (4-CPO), a potentially bidentate ligand, with manganese(II), cobalt(II), nickel(II), zinc(II), cadmium(II) and rnercury(II) thiocyanates have been prepared and characterized from their elemental analyses, magnetic susceptibilities, electronic and infrared spectral studies down to 200 cm -1 in the solid state. The compounds isolated are: Mn(4-CPO) 2(NCS) 2, Co(4-CPO) 2(NCS) 2,Ni(4-CPO) 2(NCS) 2,Zn(4-CPO) 2(NCS) 2, Cd(4-CPO)(NCS) 2 and Hg(4-CPO) 2(SCN) 2. It is shown that 4-CPO acts as a terminal N-oxide oxygen bonded monodentate ligand in all the metal(II) thiocyanate complexes studied. Tentative stereochemistries of the complexes in the solid state are discussed. The ligand field parameters 10 Dq, B, β and λ calculated for the manganese(II), cobalt(II) and nickel(II) complexes are consistent with their proposed stereochemistries.

Synthesis, analysis and radiolysis of the cobalt III 8 hydroxyquinolinate complex

International Nuclear Information System (INIS)

Mestnik, S.A.C.; Silva, C.P.G. da.

1981-11-01

The cobalt III 8-hidroxyquinolinate complex was syntetized from a solution of cobalt II. The compound was analysed by IR absorption spectroscopy, elemental analysis and by the determination of number of ligands. The radiolytic degradation was verified by spectrophotometry after submitting samples of 10 - 3 M complex in ethanolic solution to different doses of gamma radiation from a 60 Co source. The change of maximum absorbance of the complex with different doses of gamma radiation and its UV-VIS absorption spectra are presented. The complex in the solid state was also irradiated with 6,9 Mrad of gamma radiation but it didn't present degradation. (Author) [pt

Phase equilibria in the iron oxide-cobalt oxide-phosphorus oxide system

Science.gov (United States)

De Guire, Mark R.; Prasanna, T. R. S.; Kalonji, Gretchen; O'Handley, Robert C.

1987-01-01

Two novel ternary compounds are noted in the present study of 1000 C solid-state equilibria in the Fe-Co-P-O system's Fe2O3-FePO4-Co3(Po4)2-CoO region: CoFe(PO4)O, which undergoes incongruent melting at 1130 C, and Co3Fe4(PO4)6, whose incongruent melting occurs at 1080 C. The liquidus behavior-related consequences of rapidly solidified cobalt ferrite formation from cobalt ferrite-phosphate melts are discussed with a view to spinel formation. It is suggested that quenching from within the spinel-plus-liquid region may furnish an alternative to quenching a homogeneous melt.

Elicitation threshold of cobalt chloride

DEFF Research Database (Denmark)

Fischer, Louise A; Johansen, Jeanne D; Voelund, Aage

2016-01-01

: On the basis of five included studies, the ED10 values of aqueous cobalt chloride ranged between 0.0663 and 1.95 µg cobalt/cm(2), corresponding to 30.8-259 ppm. CONCLUSIONS: Our analysis provides an overview of the doses of cobalt that are required to elicit allergic cobalt contactdermatitis in sensitized...

Coordination of different ligands to copper(II) and cobalt(III) metal centers enhances Zika virus and dengue virus loads in both arthropod cells and human keratinocytes.

Science.gov (United States)

Dutta, Shovan; Celestine, Michael J; Khanal, Supreet; Huddleston, Alexis; Simms, Colin; Arca, Jessa Faye; Mitra, Amlan; Heller, Loree; Kraj, Piotr J; Ledizet, Michel; Anderson, John F; Neelakanta, Girish; Holder, Alvin A; Sultana, Hameeda

2018-01-01

Trace elements such as copper and cobalt have been associated with virus-host interactions. However, studies to show the effect of conjugation of copper(II) or cobalt(III) metal centers to thiosemicarbazone ligand(s) derived from either food additives or mosquito repellent such as 2-acetylethiazole or citral, respectively, on Zika virus (ZIKV) or dengue virus (serotype 2; DENV2) infections have not been explored. In this study, we show that four compounds comprising of thiosemicarbazone ligand derived from 2-acetylethiazole viz., (E)-N-ethyl-2-[1-(thiazol-2-yl)ethylidene]hydrazinecarbothioamide (acetylethTSC) (compound 1), a copper(II) complex with acetylethTSC as a ligand (compound 2), a thiosemicarbazone ligand-derived from citral (compound 3) and a cobalt(III) complex with a citral-thiosemicarbazone ligand (compound 4) increased DENV2 and ZIKV replication in both mosquito C6/36 cells and human keratinocytes (HaCaT cells). Treatment of both cell lines with compounds 2 or 4 showed increased dengue viral titers at all three tested doses. Enhanced dengue viral plaque formation was also noted at the tested dose of 100μM, suggesting higher production of infectious viral particles. Treatment with the compounds 2 or 4 enhanced ZIKV and DENV2 RNA levels in HeLa cell line and primary cultures of mouse bone marrow derived dendritic cells. Also, pre- or post treatments with conjugated compounds 2 or 4 showed higher loads of ZIKV or DENV2 envelope (E) protein in HaCaT cells. No changes in loads of E-protein were found in ZIKV-infected C6/36 cells, when compounds were treated after infection. In addition, we tested bis(1,10-phenanthroline)copper(II) chloride ([Cu(phen) 2 ]Cl 2 , (compound 5) and tris(1,10-phenanthroline)cobalt(III) chloride ([Co(phen) 3 ]Cl 3 , (compound 6) that also showed enhanced DENV2 loads. Also, we found that copper(II) chloride dehydrate (CuCl 2 ·2H 2 O) or cobalt(II) chloride hexahydrate (CoCl 2 ·6H 2 O) alone had no effects as "free" cations

Investigations on the formation of cobalt thiomolybdates

Energy Technology Data Exchange (ETDEWEB)

Prasad, S [Paraiba Univ., Joao Pessoa (Brazil). Dept. de Engenharia Quimica

1984-06-01

The reactions between Co/sup 2 +/ and different thiomolybdate anions (MoS/sup 2 -//sub 4/, Mo/sub 4/S/sup 6 -//sub 15/, Mo/sub 2/S/sup 2 -//sub 7/ and Mo/sub 4/S/sup 2 -//sub 13/) have been investigated by means of glass electrode and conductometric titrations between the reactants at several concentrations. The results provide definite evidence for the formation of CoS.MoS/sub 3/ and 3CoS.4MoS/sub 3/ around pH 7.1 and 5.9, respectively. The titrations of cobalt chloride with Na/sub 2/S.2MoS/sub 3/ and Na/sub 2/S.4MoS/sub 3/ failed to provide any dependable results for the formation of the corresponding cobalt thiomolybdates. The accuracy and reproducibility of these titrations are of high order. Analytical investigations of these compounds have also been carried out and substantiate the results of the pH and conductometric measurements.

Electrochemical Cobalt-Catalyzed C-H Activation.

Science.gov (United States)

Sauermann, Nicolas; Meyer, Tjark H; Ackermann, Lutz

2018-06-19

Carbon-heteroatom bonds represent omnipresent structural motifs of the vast majority of functionalized materials and bioactive compounds. C-H activation has emerged as arguably the most efficient strategy to construct C-Het bonds. Despite of major advances, these C-H transformations were largely dominated by precious transition metal catalysts, in combination with stoichiometric, toxic metal oxidants. Herein, we discuss the recent evolution of cobalt-catalyzed C-H activations that enable C-Het formations with electricity as the sole sustainable oxidant until May 2018. © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Synthesis and characterization of cobalt ferrocyanides loaded on organic anion exchanger

Energy Technology Data Exchange (ETDEWEB)

Valsala, T.P. [Waste Management Division, Bhabha Atomic Research Centre, Trombay 400 085 (India)], E-mail: tpvalsala@yahoo.co.in; Joseph, Annie [Waste Management Division, Bhabha Atomic Research Centre, Trombay 400 085 (India); Shah, J.G. [Back End Technology Division, Bhabha Atomic Research Centre, Trombay 400 085 (India); Raj, Kanwar [Waste Management Division, Bhabha Atomic Research Centre, Trombay 400 085 (India); Venugopal, V. [Radiochemistry and Isotope Group, Bhabha Atomic Research Centre, Trombay 400 085 (India)

2009-02-15

Transition metal ferrocyanides have important applications in the selective removal of radioactive caesium from low level and intermediate level radioactive liquid waste streams. The microcrystalline nature of these materials renders them useless for application in column mode operations. Special preparation procedures have been developed to prepare granular solids by in situ precipitation of metal ferrocyanides on organic anion exchangers, which is suitable for column mode operations. The elemental compositions of the metal ferrocyanides precipitated inside the pores of anion exchanger were determined by analysing the dissolved samples using ICP-AES system and flame photometer. From the XRD and EDX analyses and the elemental composition of the synthesized materials, the nature of the compound formed inside the anion exchanger was found to be cobalt ferrocyanide. From SEM analysis of the samples, the particle size of the cobalt ferrocyanide precipitated inside the anion exchanger was found to be much less than that of cobalt ferrocyanide precipitated outside. The efficiency of these materials for removal of Cs was evaluated by measuring the distribution coefficient (Kd), ion exchange capacity and kinetics of Cs uptake. The Kd of the materials loaded on anion exchanger was found to be of the order of 10{sup 5} ml/g. The Cs uptake kinetics of the materials loaded on anion exchanger was slower than that of precipitated materials. The ion exchange capacity of the cobalt ferrocyanide loaded on anion exchanger was found to be much higher than that of the precipitated cobalt ferrocyanide.

Anion effect on the retention of recoil atom of coordination crystalline compounds

International Nuclear Information System (INIS)

Dimotakis, P.N.; Papadopoulos, B.P.

1980-01-01

The anion effect of various cobaltic crystalline compounds - having the same cation and differing in anion -on the retention of neutron activated central cobalt atom has been studied. The cation was trans-dichloro(bis)ethylenediamine cobalt(III) and the anions were simple spherical anions (Cl - , Br - , I - ), planar anions (NO 3 - ), trigonal pyramidal anions (ClO 3 - , BrO 3 - ), tetrahedral anions (SO 4 2- , CrO 4 2- , MnO 4 - ) and linear anions (SCN - ). The cobalt-60 activity after reactor irradiation either in simple Co 2+ cation or in cobaltic complex cation determined the retention values. In all irradiations at ordinary temperature and at liquid nitrogen temperature the results showed an effect of the different anions, depending on the geometry, volume and charge, on the recombination of the recoil cobalt with the ligands in the coordination sphere. (author)

Co-exposure to nickel and cobalt chloride enhances cytotoxicity and oxidative stress in human lung epithelial cells

International Nuclear Information System (INIS)

Patel, Eshan; Lynch, Christine; Ruff, Victoria; Reynolds, Mindy

2012-01-01

Nickel and cobalt are heavy metals found in land, water, and air that can enter the body primarily through the respiratory tract and accumulate to toxic levels. Nickel compounds are known to be carcinogenic to humans and animals, while cobalt compounds produce tumors in animals and are probably carcinogenic to humans. People working in industrial and manufacturing settings have an increased risk of exposure to these metals. The cytotoxicity of nickel and cobalt has individually been demonstrated; however, the underlying mechanisms of co-exposure to these heavy metals have not been explored. In this study, we investigated the effect of exposure of H460 human lung epithelial cells to nickel and cobalt, both alone and in combination, on cell survival, apoptotic mechanisms, and the generation of reactive oxygen species and double strand breaks. For simultaneous exposure, cells were exposed to a constant dose of 150 μM cobalt or nickel, which was found to be relatively nontoxic in single exposure experiments. We demonstrated that cells exposed simultaneously to cobalt and nickel exhibit a dose-dependent decrease in survival compared to the cells exposed to a single metal. The decrease in survival was the result of enhanced caspase 3 and 7 activation and cleavage of poly (ADP-ribose) polymerase. Co-exposure increased the production of ROS and the formation of double strand breaks. Pretreatment with N-acetyl cysteine alleviated the toxic responses. Collectively, this study demonstrates that co-exposure to cobalt and nickel is significantly more toxic than single exposure and that toxicity is related to the formation of ROS and DSB. -- Highlights: ► Decreased survival following simultaneous exposure to NiCl 2 and CoCl 2 . ► Enhanced caspase and PARP cleavage following co-exposure. ► Increased formation of ROS in dual exposed cells. ► N-acetyl cysteine pretreatment decreases Co and Ni toxicity. ► Co-exposure to Ni and Co enhances the formation of double strand

Cobalt metabolism and toxicology—A brief update

International Nuclear Information System (INIS)

Simonsen, Lars Ole; Harbak, Henrik; Bennekou, Poul

2012-01-01

Cobalt metabolism and toxicology are summarized. The biological functions of cobalt are updated in the light of recent understanding of cobalt interference with the sensing in almost all animal cells of oxygen deficiency (hypoxia). Cobalt (Co 2+ ) stabilizes the transcriptional activator hypoxia-inducible factor (HIF) and thus mimics hypoxia and stimulates erythropoietin (Epo) production, but probably also by the same mechanism induces a coordinated up-regulation of a number of adaptive responses to hypoxia, many with potential carcinogenic effects. This means on the other hand that cobalt (Co 2+ ) also may have beneficial effects under conditions of tissue hypoxia, and possibly can represent an alternative to hypoxic preconditioning. Cobalt is acutely toxic in larger doses, and in mammalian in vitro test systems cobalt ions and cobalt metal are cytotoxic and induce apoptosis and at higher concentrations necrosis with inflammatory response. Cobalt metal and salts are also genotoxic, mainly caused by oxidative DNA damage by reactive oxygen species, perhaps combined with inhibition of DNA repair. Of note, the evidence for carcinogenicity of cobalt metal and cobalt sulfate is considered sufficient in experimental animals, but is as yet considered inadequate in humans. Interestingly, some of the toxic effects of cobalt (Co 2+ ) have recently been proposed to be due to putative inhibition of Ca 2+ entry and Ca 2+ -signaling and competition with Ca 2+ for intracellular Ca 2+ -binding proteins. The tissue partitioning of cobalt (Co 2+ ) and its time-dependence after administration of a single dose have been studied in man, but mainly in laboratory animals. Cobalt is accumulated primarily in liver, kidney, pancreas, and heart, with the relative content in skeleton and skeletal muscle increasing with time after cobalt administration. In man the renal excretion is initially rapid but decreasing over the first days, followed by a second, slow phase lasting several weeks, and

Ising-type magnetic anisotropy in a cobalt(II) nitronyl nitroxide compound: a key to understanding the formation of molecular magnetic nanowires.

Science.gov (United States)

Caneschi, A; Gatteschi, Dante; Lalioti, N; Sessoli, R; Sorace, L; Tangoulis, V; Vindigni, A

2002-01-04

The compound [Co(hfac)2-(NITPhOMe)2] (2) (hfac = hexafluoroacetylacetonate, NITPhOMe = 4'-methoxyphenyl-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide) crystallizes in the triclinic P1 space group, a= 10.870(5), b = 11.520(5), c = 19.749(5) A, alpha = 78.05(5), beta = 84.20(5), gamma = 64.51(5) degrees, Z = 2. It can be considered a model system for studying the nature of the magnetic anisotropy of [Co(hfac)2(NITPhOMe)] (1), which was recently reported to behave as a molecular magnetic wire. The magnetic anisotropy of 2 was investigated by EPR spectroscopy and SQUID magnetometry both in the polycrystalline powder and in a single crystal. The experimental magnetic anisotropy was related to the anisotropy of the central ion and to the exchange interaction between the cobalt(II) ion and the radicals.

Cobalt metabolism and toxicology-A brief update

Energy Technology Data Exchange (ETDEWEB)

Simonsen, Lars Ole, E-mail: LOSimonsen@dadlnet.dk; Harbak, Henrik; Bennekou, Poul

2012-08-15

Cobalt metabolism and toxicology are summarized. The biological functions of cobalt are updated in the light of recent understanding of cobalt interference with the sensing in almost all animal cells of oxygen deficiency (hypoxia). Cobalt (Co{sup 2+}) stabilizes the transcriptional activator hypoxia-inducible factor (HIF) and thus mimics hypoxia and stimulates erythropoietin (Epo) production, but probably also by the same mechanism induces a coordinated up-regulation of a number of adaptive responses to hypoxia, many with potential carcinogenic effects. This means on the other hand that cobalt (Co{sup 2+}) also may have beneficial effects under conditions of tissue hypoxia, and possibly can represent an alternative to hypoxic preconditioning. Cobalt is acutely toxic in larger doses, and in mammalian in vitro test systems cobalt ions and cobalt metal are cytotoxic and induce apoptosis and at higher concentrations necrosis with inflammatory response. Cobalt metal and salts are also genotoxic, mainly caused by oxidative DNA damage by reactive oxygen species, perhaps combined with inhibition of DNA repair. Of note, the evidence for carcinogenicity of cobalt metal and cobalt sulfate is considered sufficient in experimental animals, but is as yet considered inadequate in humans. Interestingly, some of the toxic effects of cobalt (Co{sup 2+}) have recently been proposed to be due to putative inhibition of Ca{sup 2+} entry and Ca{sup 2+}-signaling and competition with Ca{sup 2+} for intracellular Ca{sup 2+}-binding proteins. The tissue partitioning of cobalt (Co{sup 2+}) and its time-dependence after administration of a single dose have been studied in man, but mainly in laboratory animals. Cobalt is accumulated primarily in liver, kidney, pancreas, and heart, with the relative content in skeleton and skeletal muscle increasing with time after cobalt administration. In man the renal excretion is initially rapid but decreasing over the first days, followed by a second, slow

Cobalt Fischer-Tropsch catalysts: influence of cobalt dispersion and titanium oxides promotion

Energy Technology Data Exchange (ETDEWEB)

Azib, H

1996-04-10

The aim of this work is to study the effect of Sol-Gel preparation parameters which occur in silica supported cobalt catalysts synthesis. These catalysts are particularly used for the waxes production in natural gas processing. The solids have been characterized by several techniques: transmission electron microscopy (TEM), X-ray absorption near edge spectroscopy (XANES), programmed temperature reduction (TPR), infrared spectroscopy (IR), ultraviolet spectroscopy (UV), Magnetism, thermodesorption of H{sub 2} (TPD). The results indicate that the control of the cobalt dispersion and oxide phases nature is possible by modifying Sol-Gel parameters. The catalytic tests in Fischer-Tropsch synthesis were conducted on a pilot unit under pressure (20 atm) and suggested that turnover rates were independent of Co crystallite size, Co phases in the solids (Co deg., cobalt silicate) and titanium oxide promotion. On the other methane, the C{sub 3}{sup +} hydrocarbon selectivity is increased with increasing crystallite size. Inversely, the methane production is favoured by very small crystallites, cobalt silicate increase and titanium addition. However, the latter, used as a cobalt promoter, has a benefic effect on the active phase stability during the synthesis. (author). 149 refs., 102 figs., 71 tabs.

Cobalt accumulation and circulation by blackgum trees

International Nuclear Information System (INIS)

Thomas, W.A.

1975-01-01

Blackgum (Nyssa sylvatica Marsh.) trees accumulate far greater concentrations of cobalt in mature foliage than do other species on the same site (363 ppM in ash of blackgum, compared with about 3 ppM by mockernut hickory and about 1 ppM by red maple, tulip tree, and white oak). Cobalt concentrations in dormant woody tissues of blackgum also significantly exceed those in the other four species. Inoculation of six blackgums with 60 Co revealed that cobalt remains mobile in the trees for at least 3 years. Foliar concentrations of stable cobalt increase uniformly until senescence. In late August, foliage accounts for only 9 percent of total tree weight but 57 percent of total tree cobalt. Losses of cobalt from trees occur almost entirely by leaf abscission, and the loss rates of weight and cobalt from decomposing litter are similar. Retention of cobalt in the biologically active soil layers perpetuates zones of cobalt concentration created by this species in woodlands

Cobalt-60 production in CANDU power reactors

International Nuclear Information System (INIS)

Slack, J.; Norton, J.L.; Malkoske, G.R.

2003-01-01

MDS Nordion has been supplying cobalt-60 sources to industry for industrial and medical purposes since 1946. These cobalt-60 sources are used in many market and product segments. The major application is in the health care industry where irradiators are used to sterilize single use medical products. These irradiators are designed and built by MDS Nordion and are used by manufacturers of surgical kits, gloves, gowns, drapes and other medical products. The irradiator is a large shielded room with a storage pool for the cobalt-60 sources. The medical products are circulated through the shielded room and exposed to the cobalt-60 sources. This treatment sterilizes the medical products which can then be shipped to hospitals for immediate use. Other applications for this irradiation technology include sanitisation of cosmetics, microbial reduction of pharmaceutical raw materials and food irradiation. The cobalt-60 sources are manufactured by MDS Nordion in their Cobalt Operations Facility in Kanata. More than 75,000 cobalt-60 sources for use in irradiators have been manufactured by MDS Nordion. The cobalt-60 sources are double encapsulated in stainless steel capsules, seal welded and helium leak tested. Each source may contain up to 14,000 curies. These sources are shipped to over 170 industrial irradiators around the world. This paper will focus on the MDS Nordion proprietary technology used to produce the cobalt-60 isotope in CANDU reactors. Almost 55 years ago MDS Nordion and Atomic Energy of Canada developed the process for manufacturing cobalt-60 at the Chalk River Labs, in Ontario, Canada. A cobalt-59 target was introduced into a research reactor where the cobalt-59 atom absorbed one neutron to become cobalt-60. Once the cobalt-60 material was removed from the research reactor it was encapsulated in stainless steel and seal welded using a Tungsten Inert Gas weld. The first cobalt-60 sources manufactured using material from the Chalk River Labs were used in cancer

Electroplated zinc-cobalt alloy

International Nuclear Information System (INIS)

Carpenter, D.E.O.S.; Farr, J.P.G.

2005-01-01

Recent work on the deposition and use of ectrodeposited zinc-cobalt alloys is surveyed. Alloys containing lower of Nuclear quantities of cobalt are potentially more useful. The structures of the deposits is related to their chemical and mechanical properties. The inclusion of oxide and its role in the deposition mechanism may be significant. Chemical and engineering properties relate to the metallurgical structure of the alloys, which derives from the mechanism of deposition. The inclusion of oxides and hydroxides in the electroplate may provide evidence for this mechanism. Electrochemical impedance measurements have been made at significant deposition potentials, in alkaline electrolytes. These reveal a complex electrode behaviour which depends not only on the electrode potential but on the Co content of the electrolyte. For the relevant range of cathodic potential zinc-cobalt alloy electrodeposition occurs through a stratified interface. The formation of an absorbed layer ZnOH/sup +/ is the initial step, this inhibits the deposition of cobalt at low cathodic potentials, so explaining its 'anomalous deposition'. A porous layer of zinc forms on the adsorbed ZnOH/sup +/ at underpotential. As the potential becomes more cathodic, cobalt co- deposits from its electrolytic complex forming a metallic solid solution of Co in Zn. In electrolytes containing a high concentration of cobalt a mixed entity (ZnCo)/sub +/ is assumed to adsorb at the cathode from which a CoZn intermetallic deposits. (author)

Cobalt allergy in hard metal workers

Energy Technology Data Exchange (ETDEWEB)

Fischer, T; Rystedt, I

1983-03-01

Hard metal contains about 10% cobalt. 853 hard metal workers were examined and patch tested with substances from their environment. Initial patch tests with 1% cobalt chloride showed 62 positive reactions. By means of secondary serial dilution tests, allergic reactions to cobalt were reproduced in 9 men and 30 women. Weak reactions could not normally be reproduced. A history of hand eczema was found in 36 of the 39 individuals with reproducible positive test reactions to cobalt, while 21 of 23 with a positive initial patch test but negative serial dilution test had never had any skin problems. Hand etching and hand grinding, mainly female activities and traumatic to the hands, were found to involve the greatest risk of cobalt sensitization. 24 individuals had an isolated cobalt allergy. They had probably been sensitized by hard metal work, while the individuals, all women, who had simultaneous nickel allergy had probably been sensitized to nickel before their employment and then became sensitized to cobalt by hard metal work. A traumatic occupation, which causes irritant contact dermatitis and/or a previous contact allergy or atopy is probably a prerequisite for the development of cobalt allergy.

Pharmacokinetics of inorganic cobalt and a vitamin B12 supplement in the Thoroughbred horse: Differentiating cobalt abuse from supplementation.

Science.gov (United States)

Hillyer, L L; Ridd, Z; Fenwick, S; Hincks, P; Paine, S W

2018-05-01

While cobalt is an essential micronutrient for vitamin B 12 synthesis in the horse, at supraphysiological concentrations, it has been shown to enhance performance in human subjects and rats, and there is evidence that its administration in high doses to horses poses a welfare threat. Animal sport regulators currently control cobalt abuse via international race day thresholds, but this work was initiated to explore means of potentially adding to application of those thresholds since cobalt may be present in physiological concentrations. To devise a scientific basis for differentiation between presence of cobalt from bona fide supplementation and cobalt doping through the use of ratios. Six Thoroughbred horses were given 10 mL vitamin B 12 /cobalt supplement (Hemo-15 ® ; Vetoquinol, Buckingham, Buckinghamshire, UK., 1.5 mg B 12 , 7 mg cobalt gluconate = 983 μg total Co) as an i.v. bolus then an i.v. infusion (15 min) of 100 mg cobalt chloride (45.39 mg Co) 6 weeks later. Pre-and post-administration plasma and urine samples were analysed for cobalt and vitamin B 12 . Urine and plasma samples were analysed for vitamin B 12 using an immunoassay and cobalt concentrations were measured via ICP-MS. Baseline concentrations of cobalt in urine and plasma for each horse were subtracted from their cobalt concentrations post-administration for the PK analysis. Compartmental analysis was used for the determination of plasma PK parameters for cobalt using commercially available software. On administration of a vitamin B 12 /cobalt supplement, the ratio of cobalt to vitamin B 12 in plasma rapidly increased to approximately 3 and then rapidly declined below a ratio of 1 and then back to near baseline over the next week. On administration of 100 mg cobalt chloride, the ratio initially exceeded 10 in plasma and then declined with the lower 95% confidence interval remaining above a ratio of 1 for 7 days. For two horses with extended sampling, the plasma ratio remained above one for

COBALT SALTS PRODUCTION BY USING SOLVENT EXTRACTION

Directory of Open Access Journals (Sweden)

Liudmila V. Dyakova

2010-06-01

Full Text Available The paper deals with the extracting cobalt salts by using mixtures on the basis of tertiary amine from multicomponent solutions from the process of hydrochloride leaching of cobalt concentrate. The optimal composition for the extraction mixture, the relationship between the cobalt distribution coefficients and modifier’s nature and concentration, and the saltingout agent type have been determined. A hydrochloride extraction technology of cobalt concentrate yielding a purified concentrated cobalt solution for the production of pure cobalt salts has been developed and introduced at Severonikel combine.

Calcium-assisted reduction of cobalt ferrite nanoparticles for nanostructured iron cobalt with enhanced magnetic performance

International Nuclear Information System (INIS)

Qi, B.; Andrew, J. S.; Arnold, D. P.

2017-01-01

This paper demonstrates the potential of a calcium-assisted reduction process for synthesizing fine-grain (~100 nm) metal alloys from metal oxide nanoparticles. To demonstrate the process, an iron cobalt alloy (Fe_6_6Co_3_4) is obtained by hydrogen annealing 7-nm cobalt ferrite (CoFe_2O_4) nanoparticles in the presence of calcium granules. The calcium serves as a strong reducing agent, promoting the phase transition from cobalt ferrite to a metallic iron cobalt alloy, while maintaining high crystallinity. Magnetic measurements demonstrate the annealing temperature is the dominant factor of tuning the grain size and magnetic properties. Annealing at 700 °C for 1 h maximizes the magnetic saturation, up to 2.4 T (235 emu/g), which matches that of bulk iron cobalt.

Calcium-assisted reduction of cobalt ferrite nanoparticles for nanostructured iron cobalt with enhanced magnetic performance

Energy Technology Data Exchange (ETDEWEB)

Qi, B. [University of Florida, Interdisciplinary Microsystems Group, Department of Electrical and Computer Engineering (United States); Andrew, J. S. [University of Florida, Department of Materials Science and Engineering (United States); Arnold, D. P., E-mail: darnold@ufl.edu [University of Florida, Interdisciplinary Microsystems Group, Department of Electrical and Computer Engineering (United States)

2017-03-15

This paper demonstrates the potential of a calcium-assisted reduction process for synthesizing fine-grain (~100 nm) metal alloys from metal oxide nanoparticles. To demonstrate the process, an iron cobalt alloy (Fe{sub 66}Co{sub 34}) is obtained by hydrogen annealing 7-nm cobalt ferrite (CoFe{sub 2}O{sub 4}) nanoparticles in the presence of calcium granules. The calcium serves as a strong reducing agent, promoting the phase transition from cobalt ferrite to a metallic iron cobalt alloy, while maintaining high crystallinity. Magnetic measurements demonstrate the annealing temperature is the dominant factor of tuning the grain size and magnetic properties. Annealing at 700 °C for 1 h maximizes the magnetic saturation, up to 2.4 T (235 emu/g), which matches that of bulk iron cobalt.

The effect of organics on the sorption of cobalt by glacial sand in laboratory batch experiments

International Nuclear Information System (INIS)

Haigh, D.G.; Williams, G.M.; Hooker, P.J.; Ross, C.A.M.; Allen, M.R.; Warwick, P.

1989-01-01

Acetate, EDTA and organic compounds naturally present in groundwater at the Drigg in situ radionuclide migration experimental site, have been studied to assess their effect on the sorption of cobalt by glacial sand in a series of batch experiments. Removing 56% of the natural organic material from the grounwater with DEAE cellulose increased the distribution ratio (R d ) of cobalt by a factor of about two. EDTA had a dramatic effect on the sorption of Co even at low concentrations, reducing the R d by up to two orders of magnitude. At EDTA concentrations greater than 5 mg/l, there was no further reduction in sorption. EDTA was not itself sorbed, but formed a mobile complex with Co. Differences in distribution ratios were observed depending on whether the cobalt was added before or after EDTA. Within the same period of equilibrium, the R d values were higher when cobalt was allowed to equilibrate with the sand before adding EDTA. The desorption of cobalt from the mineral surface may be a rate-limiting step such that equilibrium was not achieved within the 14-day period of these experiments. Acetate had no effect on cobalt sorption in any of the experiments undertaken. This work is part of the Commission Mirage project, Phase 2, research area Geochemistry of actinides and fission products in natural aquifer systems

Nickel acts as an adjuvant during cobalt sensitization

DEFF Research Database (Denmark)

Bonefeld, Charlotte Menne; Nielsen, Morten Milek; Vennegaard, Marie T.

2015-01-01

Metal allergy is the most frequent form of contact allergy with nickel and cobalt being the main culprits. Typically, exposure comes from metal-alloys where nickel and cobalt co-exist. Importantly, very little is known about how co-exposure to nickel and cobalt affects the immune system. We...... investigated these effects by using a recently developed mouse model. Mice were epicutaneously sensitized with i) nickel alone, ii) nickel in the presence of cobalt, iii) cobalt alone, or iv) cobalt in the presence of nickel, and then followed by challenge with either nickel or cobalt alone. We found...... that sensitization with nickel alone induced more local inflammation than cobalt alone as measured by increased ear-swelling. Furthermore, the presence of nickel during sensitization to cobalt led to a stronger challenge response to cobalt as seen by increased ear-swelling and increased B and T cell responses...

Use of some inorganic and organic compounds as decontaminants for cobalt-60 and caesium-134 by clover plant grown on Inshas sandy soil

Energy Technology Data Exchange (ETDEWEB)

Abdel Sabour, M.F.; El-Naggar, H.A.; Soliman, S.M. (Atomic Energy Establishment, Cairo (Egypt). Nuclear Chemistry Dept.)

1991-01-01

Outdoor lysimeter experiments were carried out to elucidate the effect of 4 inorganic and 3 organic salts on {sup 60}Co and {sup 134}Cs uptake and dry matter yield of three cuts of clover in the soils of Inshas. A new concept was proposed for assessing the difference in capacity of soil to supply radionuclides to plants as affected by applied inorganic or organic compounds. A relation of plant tissue radionuclide content with time can be expressed in an exponential equation with corresponding regression coefficients. When the same plant species is grown on the same soil differing only in the applied compounds (e.g. Fe-EDDHA, Fe-DTPA, Fe-OAC, Fe(COO){sub 2}, Al(OH){sub 3}, Ca(H{sub 2}PO{sub 4}){sub 2}, Fe{sub 2}O{sub 3}) the derived equation will change. Differences of either Co or Cs accumulation with time between control and any other treatment were evaluated. The data also show that Fe-DTPA is preferred for {sup 60}Co as enhancing compound for plant uptake (for decontamination use), compared with other applied salts, on the other hand, any tested salts did not significantly effect {sup 134}Cs taken by clover. It was also found that more than 70% of the total cobalt uptake was accumulated in the roots which indicate that Co is less mobile in plants than Cs. (orig.).

Use of some inorganic and organic compounds as decontaminants for cobalt-60 and caesium-134 by clover plant grown on Inshas sandy soil

International Nuclear Information System (INIS)

Abdel Sabour, M.F.; El-Naggar, H.A.; Soliman, S.M.

1991-01-01

Outdoor lysimeter experiments were carried out to elucidate the effect of 4 inorganic and 3 organic salts on 60 Co and 134 Cs uptake and dry matter yield of three cuts of clover in the soils of Inshas. A new concept was proposed for assessing the difference in capacity of soil to supply radionuclides to plants as affected by applied inorganic or organic compounds. A relation of plant tissue radionuclide content with time can be expressed in an exponential equation with corresponding regression coefficients. When the same plant species is grown on the same soil differing only in the applied compounds (e.g. Fe-EDDHA, Fe-DTPA, Fe-OAC, Fe(COO) 2 , Al(OH) 3 , Ca(H 2 PO 4 ) 2 , Fe 2 O 3 ) the derived equation will change. Differences of either Co or Cs accumulation with time between control and any other treatment were evaluated. The data also show that Fe-DTPA is preferred for 60 Co as enhancing compound for plant uptake (for decontamination use), compared with other applied salts, on the other hand, any tested salts did not significantly effect 134 Cs taken by clover. It was also found that more than 70% of the total cobalt uptake was accumulated in the roots which indicate that Co is less mobile in plants than Cs. (orig.) [de

Cobalt-60 production in CANDU reactors

International Nuclear Information System (INIS)

Ross, Michel; Lemire, Christian

2002-01-01

CANDU reactors can produce cobalt-60 very efficiently and with an interesting return on investment. This paper discusses what is needed to convert a CANDU reactor into a cobalt-60 producer: what are the different phases, the safety studies required, the physical modifications needed, and what is the minimum involvement of the utility owning the plant. The past ten years of experience of Hydro-Quebec as a cobalt-60 producer will be reviewed, including the management of the risk of both incident and electricity generation loss, and including the benefits for the utility and its personnel. Originally a simple metal used for centuries as a pigment, cobalt-59 today is transformed into cobalt-60, a radioactive element of unprecedented value. Well known in medicine for cancer treatment, cobalt-60 is also used to sterilize a wide range of disposable medical products used in hospitals and to sanitize pharmaceutical and cosmetic products. Cobalt-60 is proving to be a new and effective solution, in the food sector, for preserving harvests and controlling food-borne diseases, or to advantageously replace certain gases and chemical products which are suspected of being harmful or carcinogenic. There are also other applications, such as: hardening of some plastics, treatment of sewage sludge and elimination of harmful insect populations. With a half-life of 5,3 years, cobalt-60 is a metal not found in nature. It is a radioactive isotope produced by exposing stable nuclei of cobalt-59 to neutrons. One of the best places to find such an important neutron source is a nuclear reactor. High energy gamma rays are then emitted during the process of radioactive decay, where cobalt-60 seeks again its stable state

Crystalline and amorphous rare-earth metallic compounds

International Nuclear Information System (INIS)

Burzo, E.

1975-01-01

During the last years the study of magnetic behaviour of rare-earth (or yttrium) compounds with cobalt and iron has growth of interest. This interest of justified by a large area of experimental and theoretical problems coming into being in the study of some rare-earth materials as well as in their technical applications. In the last three years a great number of new rare earth materials were studied and also new models explaining the magnetic behaviour of these systems have been used. In this paper we refer especially to some typical systems in order to analyse the magnetic behaviour of iron and cobalt and also the part played by the magnetic interactions in the values of the cobalt or iron moments. The model used will be generally the molecular field model. In the second chapter we present comparatively the structure of crystalline and amorphous compounds for further correlation with the magnetic properties. In chapter III we analyse the magnetic interactions in some crystalline and amorphous rare-earth alloys. Finally, we exemplify the ways in which we ensure better requried characteristics by the technical utilizations of these materials. These have in view the modifications of the magnetic interactions and are closely related with the analysis made in chapter III

Process for the elimination of organic compounds in solution or in suspension from an aqueous solution such as a radioactive effluent

International Nuclear Information System (INIS)

Cordero, G.; Gauthier, F.; Perotin, J.P.; Saulze, J.L.

1991-01-01

Organic compounds such as complexing agents (for instance citric acid, EDTA and tartric acid) are oxidized with Co 3+ ions. For this purpose a cobalt (II) salt is added to the aqueous solution and Co 3+ ions required for oxidation are continuously generated by electrolysis. The cobalt salt is preferentially cobalt nitrate [fr

Electrocatalytic performance evaluation of cobalt hydroxide and cobalt oxide thin films for oxygen evolution reaction

Science.gov (United States)

Babar, P. T.; Lokhande, A. C.; Pawar, B. S.; Gang, M. G.; Jo, Eunjin; Go, Changsik; Suryawanshi, M. P.; Pawar, S. M.; Kim, Jin Hyeok

2018-01-01

The development of an inexpensive, stable, and highly active electrocatalyst for oxygen evolution reaction (OER) is essential for the practical application of water splitting. Herein, we have synthesized an electrodeposited cobalt hydroxide on nickel foam and subsequently annealed in an air atmosphere at 400 °C for 2 h. In-depth characterization of all the films using X-ray diffraction (XRD), X-ray photoelectron emission spectroscopy (XPS), field emission scanning electron microscopy (FE-SEM), electrochemical impedance spectroscopy (EIS) and linear sweep voltammetry (LSV) techniques, which reveals major changes for their structural, morphological, compositional and electrochemical properties, respectively. The cobalt hydroxide nanosheet film shows high catalytic activity with 290 mV overpotential at 10 mA cm-2 and 91 mV dec-1 Tafel slope and robust stability (24 h) for OER in 1 M KOH electrolyte compared to cobalt oxide (340 mV). The better OER activity of cobalt hydroxide in comparison to cobalt oxide originated from high active sites, enhanced surface, and charge transport capability.

Cobalt sensitization and dermatitis

DEFF Research Database (Denmark)

Thyssen, Jacob P

2012-01-01

: This clinical review article presents clinical and scientific data on cobalt sensitization and dermatitis. It is concluded that cobalt despite being a strong sensitizer and a prevalent contact allergen to come up on patch testing should be regarded as a very complex metal to test with. Exposure...

Cobalt 60 availability for radiation processing

International Nuclear Information System (INIS)

Fraser, F.M.

1986-01-01

In the last 20 years, the steady and significant growth in the application of radiation processing to industrial sterilization has been seen. The principal application of this technology is the sterilization of disposable medical products, food irradiation, the irradiation of personal care goods and so on. At present, more than 70 million curies of cobalt-60 supplied by Atomic Energy of Canada Ltd. have been used for gamma processing in these applications. This is estimated to be more than 80 % of the total cobalt-60 in service in the world. Commercial food irradiation has an exciting future, and as to the impact of food irradiation on the availability of cobalt-60 over the next ten years, two principal factors must be examined, namely, the anticipated demand for cobalt-60 in all radiation processing applications, and the supply of cobalt-60 to reliably meet the expected demand. As for the cobalt-60 in service today, 90 % is used for the sterilization of disposable medical products, 5 % for food irradiation, and 5 % for other application. The demand for up to 30 million curies of cobalt-60 is expected over the next 10 years. Today, it is estimated that over 150,000 tons of spices, fruit and fish are irradiated. The potential cobalt-60 production could exceed 110 million curies per year. Gamma processing application will demand nearly 50 million curies in 1990. (Kako, I.)

Synthesis and characterization of cobalt-nichel oxides for the oxygen formation reaction

International Nuclear Information System (INIS)

Morales G, P.

2001-01-01

In this work the compounds of cobalt and nickel oxides and the mixtures of cobalt-nickel were prepared which were characterized and evaluated as electrocatalysts in the oxygen release reaction in alkaline media. The compounds were synthesised by the sol-gel method: heated at 400 and 500 Centigrade. The compounds characterization was realized by thermogravimetry, X-ray diffraction and Scanning electron microscopy. As the Co 3 O 4 and the Ni O as the mixtures Ni O/Co 3 O 4 were obtained as a porous material with a small particle size, characteristics which are presented by cause of the low temperature of synthesis. The electrocatalytic evaluation for the synthesised compounds for the oxygen release reaction was realized by cyclic volt amperometry in a 0.5M KOH solution. The oxides mixtures presented a well electrocatalytic activity to be used in the electrochemical release of oxygen. The current density and the electrochemically active area, in all the cases of mixtures is very higher to the Co 3 O 4 and Ni O ones. Observing with greater clearness the synergic effects, in the obtained mixture at 400 C. The oxides mixtures heated at 400 C were stables for the oxygen formation reaction. Therefore it is be able to say that the Ni O/Co 3 O 4 mixture counts on a great reactive area: electrocatalytic characteristic desirable to be a material used as anode in the electrolysis of water, which increases the oxygen release in the anode and so the hydrogen release in the cathode. (Author)

Cobalt-doped ZnO as dilute magnetic semiconductor; Cobalt dotiertes ZnO als verduennter magnetischer Halbleiter

Energy Technology Data Exchange (ETDEWEB)

Gacic, Milan

2009-04-24

Dilute magnetic semiconductors (DMS) are technologically promising materials that show ferromagnetic as well as semiconducting properties. These are one of the crucial compounds concerning the development of spintronic devices. The main problem so far ist that for applications the Curie temperature of most of the DMS compounds is much too low. However, DMS compounds based on ZnO as Zn{sub 1-x}Co{sub x}O seem to show ferromagnetism above room temperature, but the ferromagnetic exchange is not fully understood. Intensive experimental investigations need to be done. In the course of this theses Zn{sub 0.95}Co{sub 0.05}O thin films were fabricated by pulsed laser deposition and investigated concerning their magnetic, magnetoelectric and structural properties in order to understand the ferromagnetism in this material. Different experimental methods have been used, as magnetometry, X-ray diffraction (XRD), X-ray magnetic circular dichroism (XMCD), electron spin resonance (ESR) and magnetoelectric transport measurements. At special preparation conditions, where a high defect density is induced, the samples are clearly ferromagnetic above room temperature with a saturation magnetization of 2 {mu}{sub b}/Co and a remanence of 90%. Electrical transport measurements show a clear magnetoresistance as well as a anomalous Hall effect. The anomalous Hall effect rises with the magnetization indicating intrinsic ferromagnetism and a certain degree of spin polarization. As the ferromagnetism disappears with rising charge carrier density the ferromagnetic interaction cannot be mediated by the conduction electrons. A more precise evaluation of the magnetoelectric results shows that there is an additional conducting impurity band which could even be spinpolarized. So there are indications that the ferromagnetism is due to magnetic polarons. Some of the structural and magnetometric results as well as the electron spin resonance measurements suggest an additional extrinsic contribution

Aerobic Oxidation of Alcohols to Carbonyl Compounds Catalyzed by ...

Indian Academy of Sciences (India)

Hydrotalcite-like compounds; cobalt porphyrin; alcohol oxidation; ... cient catalytic method for the low temperature oxy- ... nitrate,8 acetaldehyde,9 ammonium salts10 and NO2,11 ..... N, Sakurai H and Tsukuda T 2009 Effect of electronic.

Exploration of Cocatalyst Effects on a Bimetallic Cobalt Catalyst System: Enhanced Activity and Enantioselectivity in Epoxide Polymerization

KAUST Repository

Widger, Peter C. B.; Ahmed, Syud M.; Coates, Geoffrey W.

2011-01-01

Organic ionic compounds were synthesized and investigated as cocatalysts with a bimetallic cobalt complex for enantioselective epoxide polymerization. The identities of both the cation and the anion were systematically varied, and the subsequent reactivity was studied. The nature of the ionic cocatalyst dramatically impacted the rate and enantioselectivity of the catalyst system. The ionic cocatalyst [P(N=P(N(CH2)4)3) 4 +][tBuCO2 -] in combination with a bimetallic cobalt complex produced a catalyst system that exhibited the greatest activity and selectivity for a variety of monosubstituted epoxides. © 2011 American Chemical Society.

Exploration of Cocatalyst Effects on a Bimetallic Cobalt Catalyst System: Enhanced Activity and Enantioselectivity in Epoxide Polymerization

KAUST Repository

Widger, Peter C. B.

2011-07-26

Organic ionic compounds were synthesized and investigated as cocatalysts with a bimetallic cobalt complex for enantioselective epoxide polymerization. The identities of both the cation and the anion were systematically varied, and the subsequent reactivity was studied. The nature of the ionic cocatalyst dramatically impacted the rate and enantioselectivity of the catalyst system. The ionic cocatalyst [P(N=P(N(CH2)4)3) 4 +][tBuCO2 -] in combination with a bimetallic cobalt complex produced a catalyst system that exhibited the greatest activity and selectivity for a variety of monosubstituted epoxides. © 2011 American Chemical Society.

Kinetic Control of Intralayer Cobalt Coordination in Layered Hydroxides: CoxoctCoxtet(OH)2(Cl)x(H2O)n

International Nuclear Information System (INIS)

Neilson, James R.; Schwenzer, Birgit; Seshadri, Ram; Morse, Daniel E.

2009-01-01

We report the synthesis and characterization of new structural variants of the isotypic compound with the generic chemical formula, Co 1-0.5x oct Co x tet (OH) 2 (Cl) x (H 2 O) n , all modifications of an α-Co(OH) 2 lattice. We show that the occupancy of tetrahedrally coordinated cobalt sites and associated chloride ligands, x, is modulated by the rate of formation of the respective layered hydroxide salts from kinetically controlled aqueous hydrolysis at an air-water interface. This new level of structural control is uniquely enabled by the slow diffusion of a hydrolytic catalyst, a simple technique. Independent structural characterizations of the compounds separately describe various attributes of the materials on different length scales, revealing details hidden by the disordered average structures. The precise control over the population of distinct octahedrally and tetrahedrally coordinated cobalt ions in the lattice provides a gentle, generic method for modulating the coordination geometry of cobalt in the material without disturbing the lattice or using additional reagents. A mechanism is proposed to reconcile the observation of the kinetic control of the structure with competing interactions during the initial stages of hydrolysis and condensation.

Synthesis of new cobalt aluminophosphate framework by opening a cobalt methylphosphonate layered material

Czech Academy of Sciences Publication Activity Database

Zaarour, M.; Pérez, O.; Boullay, P.; Martens, J.; Mihailova, B.; Karaghiosoff, K.; Palatinus, Lukáš; Mintova, S.

2017-01-01

Roč. 19, č. 34 (2017), s. 5100-5105 ISSN 1466-8033 Institutional support: RVO:68378271 Keywords : cobalt aluminophosphate * cobalt methylphosphonate * layered materials * crystallic structure * X-ray diffraction Subject RIV: BM - Solid Matter Physics ; Magnetism OBOR OECD: Condensed matter physics (including formerly solid state physics, supercond.) Impact factor: 3.474, year: 2016

Radio cobalt in French rivers

International Nuclear Information System (INIS)

Lambrechts, A.; Baudin-Jaulent, Y.

1996-01-01

The isotopes 58 and 60 of cobalt present in liquid wastes from nuclear plants or from fuel reprocessing plant of Marcoule are fixed in the different compartments of French rivers. The activity levels of radio-cobalt vary according to the sampled compartments nature (bryophyta > immersed plants > sediment > fish). Elsewhere, laboratory experimentations show that the contamination of fish occurs essentially from the water way rather than from food. Cobalt is mainly fixed by kidneys; muscles is no more than 30 % of the total fish activity. (author)

Molecular mechanics calculations on cobalt phthalocyanine dimers

NARCIS (Netherlands)

Heuts, J.P.A.; Schipper, E.T.W.M.; Piet, P.; German, A.L.

1995-01-01

In order to obtain insight into the structure of cobalt phthalocyanine dimers, molecular mechanics calculations were performed on dimeric cobalt phthalocyanine species. Molecular mechanics calculations are first presented on monomeric cobalt(II) phthalocyanine. Using the Tripos force field for the

AN ELECTROPLATING METHOD OF FORMING PLATINGS OF NICKEL, COBALT, NICKEL ALLOYS OR COBALT ALLOYS

DEFF Research Database (Denmark)

1997-01-01

An electroplating method of forming platings of nickel, cobalt, nickel alloys or cobalt alloys with reduced stresses in an electrodepositing bath of the type: Watt's bath, chloride bath or a combination thereof, by employing pulse plating with periodic reverse pulse and a sulfonated naphthalene...

Synthesis and characterization of mixtures of cobalt and titanium oxides by mechanical alloyed and Sol-Gel

International Nuclear Information System (INIS)

Basurto S, R.; Bonifacio M, J.; Fernandez V, S. M.

2009-01-01

The mechanical alloyed techniques continued by combustion and Sol-Gel method, were used for the synthesis of CoTiO 3 . With the first technique was used Co 3 O 4 obtained in a balls mill SPEX in argon atmosphere, using cobalt nitrate and urea, the combustion is realized at 400 and 500 C, the characterization by X-ray diffraction showed the obtaining of the valence oxide mixed of cobalt with crystallite size from 10 to 12.5 nm and the particle size of 60 to 75 nm was obtained by scanning electron microscopy. To prepare the CoTiO 3 , the obtained Co 3 O 4 was mixed with TiO 2 on a relationship in weight (1:1) and with a milling time of 2.5 h and the combustion at 800 C. the mixed oxide of titanium cobalt was also obtained by the Sol-Gel technique starting from cobalt chloride and titanium propoxide in acetic-water acid, the gel is burned to temperature of 300, 500, 700 and 900 C, finding that this last temperature it is that provides the compound with crystalline size from 50 to 75 nm. (Author)

Mechanism of caesium ion exchange on potassium cobalt hexacyanoferrates(II)

International Nuclear Information System (INIS)

Lehto, J.; Haukka, S.; Harjula, R.; Blomberg, M.

1990-01-01

The caesium uptakes by K 2 [CoFe(CN) 6 ] and non-stoicheiometric compounds K 2/x Co x/2 [CoFe(CN) 6 ] were found to correlate directly with the specific surface areas of the products with x 1 are mixtures of cubic potassium cobalt hexacyanoferrate (ii) and tetragonal Co 2 Fe(CN) 6 . The thermodynamic equilibrium constant of the caesium exchange on K 2 [CoFe(CN) 6 ] was found to have a high value of 125. (author)

Preliminary results about Electrodeposition of Cobalt at laboratory level

International Nuclear Information System (INIS)

Cornejo, N.

1992-01-01

As of an organic compound, an extraction and Cobalt electrodeposition method had been developed as a part of fabrication aim of a sealed radioactive source with objective to the construction of density meter prototype. It was performed preliminary test of electrodeposition in the laboratory level in a simple cell. The used electrolyte had been a sulphate solution obtained by extraction of an organic solution. It is obtained a Co film by electrodeposition at 55 o C temperature and with an approximately Co concentration in 70 g/lt. (Author) 3 refs., 1 fig., 1 tab

Thermal properties of rare earth cobalt oxides and of La1- x Gd x CoO3 solid solutions

Science.gov (United States)

Orlov, Yu. S.; Dudnikov, V. A.; Gorev, M. V.; Vereshchagin, S. N.; Solov'ev, L. A.; Ovchinnikov, S. G.

2016-05-01

Powder X-ray diffraction data for the crystal structure, phase composition, and molar specific heat for La1‒ x Gd x CoO3 cobaltites in the temperature range of 300-1000 K have been analyzed. The behavior of the volume thermal expansion coefficient in cobaltites with isovalent doping in the temperature range of 100-1000 K is studied. It is found that the β( T) curve exhibits two peaks at some doping levels. The rate of the change in the occupation number for the high-spin state of cobalt ions is calculated for the compounds under study taking into account the spin-orbit interaction. With the Birch-Murnaghan equation of state, it is demonstrated that the low-temperature peak in the thermal expansion shifts with the growth of the pressure toward higher temperatures and at pressure P ˜ 7 GPa coincides with the second peak. The similarity in the behavior of the thermal expansion coefficient in the La1- x Gd x CoO3 compounds with the isovalent substitution and the undoped LnCoO3 compound (Ln is a lanthanide) is considered. For the whole series of rare earth cobalt oxides, the nature of two specific features in the temperature dependence of the specific heat and thermal expansion is revealed and their relation to the occupation number for the high-spin state of cobalt ions and to the insulator-metal transition is established.

Cobalt reduction of NSSS valve hardfacings for ALARA

Energy Technology Data Exchange (ETDEWEB)

Kim, Joo Hak; Lee, Sang Sub [Korea Atomic Energy Research Institute, Taejon (Korea, Republic of)

1994-07-01

This report informs NSSS designer that replacement of materials is one of the major means of ALARA implementation, and describes that NSSS valves with high-cobalt hardfacing are significant contributors to post-shutdown radiation fields caused by activation of cobalt-59 to cobalt-60. Generic procedures for implementing cobalt reduction programs for valves are presented. Discussions are presented of the general and specific design requirements for valve hardfacing in nuclear service. The nuclear safety issues involved with changing valve hardfacing materials are discussed. The common methods used to deposit hardfacing materials are described together with an explanation of the wear measurements. Wear resistance, corrosion resistance, friction coefficient, and mechanical properties of candidate hardfacing alloys are given. World-wide nuclear utility experience with cobalt-free hardfacing alloys is described. The use of low-cobalt or cobalt-free alloys in other nuclear plant components is described. 17 figs., 38 tabs., 18 refs. (Author).

Cobalt reduction of NSSS valve hardfacings for ALARA

International Nuclear Information System (INIS)

Kim, Joo Hak; Lee, Sang Sub

1994-07-01

This report informs NSSS designer that replacement of materials is one of the major means of ALARA implementation, and describes that NSSS valves with high-cobalt hardfacing are significant contributors to post-shutdown radiation fields caused by activation of cobalt-59 to cobalt-60. Generic procedures for implementing cobalt reduction programs for valves are presented. Discussions are presented of the general and specific design requirements for valve hardfacing in nuclear service. The nuclear safety issues involved with changing valve hardfacing materials are discussed. The common methods used to deposit hardfacing materials are described together with an explanation of the wear measurements. Wear resistance, corrosion resistance, friction coefficient, and mechanical properties of candidate hardfacing alloys are given. World-wide nuclear utility experience with cobalt-free hardfacing alloys is described. The use of low-cobalt or cobalt-free alloys in other nuclear plant components is described. 17 figs., 38 tabs., 18 refs. (Author)

The Role of External Inputs and Internal Cycling in Shaping the Global Ocean Cobalt Distribution: Insights From the First Cobalt Biogeochemical Model

Science.gov (United States)

Tagliabue, Alessandro; Hawco, Nicholas J.; Bundy, Randelle M.; Landing, William M.; Milne, Angela; Morton, Peter L.; Saito, Mak A.

2018-04-01

Cobalt is an important micronutrient for ocean microbes as it is present in vitamin B12 and is a co-factor in various metalloenzymes that catalyze cellular processes. Moreover, when seawater availability of cobalt is compared to biological demands, cobalt emerges as being depleted in seawater, pointing to a potentially important limiting role. To properly account for the potential biological role for cobalt, there is therefore a need to understand the processes driving the biogeochemical cycling of cobalt and, in particular, the balance between external inputs and internal cycling. To do so, we developed the first cobalt model within a state-of-the-art three-dimensional global ocean biogeochemical model. Overall, our model does a good job in reproducing measurements with a correlation coefficient of >0.7 in the surface and >0.5 at depth. We find that continental margins are the dominant source of cobalt, with a crucial role played by supply under low bottom-water oxygen conditions. The basin-scale distribution of cobalt supplied from margins is facilitated by the activity of manganese-oxidizing bacteria being suppressed under low oxygen and low temperatures, which extends the residence time of cobalt. Overall, we find a residence time of 7 and 250 years in the upper 250 m and global ocean, respectively. Importantly, we find that the dominant internal resupply process switches from regeneration and recycling of particulate cobalt to dissolution of scavenged cobalt between the upper ocean and the ocean interior. Our model highlights key regions of the ocean where biological activity may be most sensitive to cobalt availability.

Synthesis, characterization and polymerization of methacrylates of copper (II), cobalt (II) and molybdenum (II). Generation of new materials

International Nuclear Information System (INIS)

Rojas Bolanos, Omar

2006-01-01

Coordination compounds of the species copper (II), cobalt (II) and molybdenum (II) with methacrylic acid were synthesized and characterized. Besides, it realized reactions of bromine addition to the doubles links of the species obtained previously, also too like reactions with dry HCl. Finally, it got hybrids materials by polymerization of the first compounds in an acrylic matrix. Research concluded with the characterization of all the products. (author) [es

Syntheses, Characterization, Resolution, and Biological Studies of Coordination Compounds of Aspartic Acid and Glycine

Science.gov (United States)

Akinkunmi, Ezekiel; Ojo, Isaac; Adebajo, Clement; Isabirye, David

2017-01-01

Enantiomerically enriched coordination compounds of aspartic acid and racemic mixtures of coordination compounds of glycine metal-ligand ratio 1 : 3 were synthesized and characterized using infrared and UV-Vis spectrophotometric techniques and magnetic susceptibility measurements. Five of the complexes were resolved using (+)-cis-dichlorobis(ethylenediamine)cobalt(III) chloride, (+)-bis(glycinato)(1,10-phenanthroline)cobalt(III) chloride, and (+)-tris(1,10-phenanthroline)nickel(II) chloride as resolving agents. The antimicrobial and cytotoxic activities of these complexes were then determined. The results obtained indicated that aspartic acid and glycine coordinated in a bidentate fashion. The enantiomeric purity of the compounds was in the range of 22.10–32.10%, with (+)-cis-dichlorobis(ethylenediamine)cobalt(III) complex as the more efficient resolving agent. The resolved complexes exhibited better activity in some cases compared to the parent complexes for both biological activities. It was therefore inferred that although the increase in the lipophilicity of the complexes may assist in the permeability of the complexes through the cell membrane of the pathogens, the enantiomeric purity of the complexes is also of importance in their activity as antimicrobial and cytotoxic agents. PMID:28293149

Accumulation of cobalt by cephalopods

International Nuclear Information System (INIS)

Nakahara, Motokazu

1981-01-01

Accumulation of cobalt by cephalopod mollusca was investigated by radiotracer experiments and elemental analysis. In the radiotracer experiments, Octopus vulgaris took up cobalt-60 from seawater fairly well and the concentration of the nuclide in whole body attained about 150 times the level of seawater at 25th day at 20 0 C. Among the tissues and organs measured, branchial heart which is the specific organ of cephalopods showed the highest affinity for the nuclide. The organ accumulated about 50% of the radioactivity in whole body in spite of its little mass as 0.2% of total body weight. On the other hand, more than 90% of the radioactivity taken up from food (soft parts of Gomphina melanaegis labelled with cobalt-60 previously in an aquarium) was accumulated in liver at 3rd day after the single administration and then the radioactivity in the liver seemed to be distributed to other organs and tissues. The characteristic elution profiles of cobalt-60 was observed for each of the organs and tissues in Sephadex gel-filtration experiment. It was confirmed by the gel-filtration that most of cobalt-60 in the branchial heart was combined with the constituents of low molecular weights. The average concentration of stable cobalt in muscle of several species of cephalopods was 5.3 +- 3.0 μg/kg wet and it was almost comparable to the fish muscle. On the basis of soft parts, concentration of the nuclide closed association among bivalve, gastropod and cephalopod except squid that gave lower values than the others. (author)

Cobalt-free nickel-base superalloys

International Nuclear Information System (INIS)

Koizumi, Yutaka; Yamazaki, Michio; Harada, Hiroshi

1979-01-01

Cobalt-free nickel-base cast superalloys have been developed. Cobalt is considered to be a beneficial element to strengthen the alloys but should be eliminated in alloys to be used for direct cycle helium turbine driven by helium gas from HTGR (high temp. gas reactor). The elimination of cobalt is required to avoid the formation of radioactive 60 Co from the debris or scales of the alloys. Cobalt-free alloys are also desirable from another viewpoint, i.e. recently the shortage of the element has become a serious problem in industry. Cobalt-free Mar-M200 type alloys modified by the additions of 0.15 - 0.2 wt% B and 1 - 1.5 wt% Hf were found to have a creep rupture strength superior or comparable to that of the original Mar-M200 alloy bearing cobalt. The ductility in tensile test at 800 0 C, as cast or after prolonged heating at 900 0 C (the tensile test was done without removing the surface layer affected by the heating), was also improved by the additions of 0.15 - 0.2% B and 1 - 1.5% Hf. The morphology of grain boundaries became intricated by the additions of 0.15 - 0.2% B and 1 - 1.5% Hf, to such a degree that one can hardly distinguish grain boundaries by microscopes. The change in the grain boundary morphology was considered, as suggested previously by one of the authors (M.Y.), to be the reason for the improvements in the creep rupture strength and tensile ductility. (author)

Structural and physical properties of a novel misfit-layered cobalt oxide (CaOH)1.14CoO2

International Nuclear Information System (INIS)

Isobe, Masaaki; Shizuya, Mitsuyuki; Takayama-Muromachi, Eiji

2007-01-01

We have studied crystal structure and physical properties of a new layered cobalt oxide (CaOH) 1.14 CoO 2 . The compound is a composite crystal which consists of two interpenetrating subsystems of the CdI 2 -type CoO 2 layer and the rock-salt-type double CaOH atomic layer. The two subsystems have incommensurate periodicity along the a-axis, resulting in modulated crystal structure due to the inter-subsystem interaction. We found that the observed physical properties originate in the electronic state with a 'low-carrier-density limit' in the cobalt t 2g band

Cobalt-60 production in CANDU power reactors

International Nuclear Information System (INIS)

Malkoske, G.R.; Norton, J.L.; Slack, J.

2002-01-01

MDS Nordion has been supplying cobalt-60 sources to industry for industrial and medical purposes since 1946. These cobalt-60 sources are used in many market and product segments, but are primarily used to sterilize single-use medical products including; surgical kits, gloves, gowns, drapes, and cotton swabs. Other applications include sanitization of cosmetics, microbial reduction of pharmaceutical raw materials, and food irradiation. The technology for producing the cobalt-60 isotope was developed by MDS Nordion and Atomic Energy of Canada Limited (AECL) almost 55 years ago using research reactors at the AECL Chalk River Laboratories in Ontario, Canada. The first cobalt-60 source produced for medical applications was manufactured by MDS Nordion and used in cancer therapy. The benefits of cobalt-60 as applied to medical product manufacturing, were quickly realized and the demand for this radioisotope quickly grew. The same technology for producing cobalt-60 in research reactors was then designed and packaged such that it could be conveniently transferred to a utility/power reactor. In the early 1970's, in co-operation with Ontario Power Generation (formerly Ontario Hydro), bulk cobalt-60 production for industrial irradiation applications was initiated in the four Pickering A CANDU reactors. As the demand and acceptance of sterilization of medical products grew, MDS Nordion expanded its bulk supply by installing the proprietary Canadian technology for producing cobalt-60 in additional CANDU reactors. CANDU is unique among the power reactors of the world, being heavy water moderated and fuelled with natural uranium. They are also designed and supplied with stainless steel adjusters, the primary function of which is to shape the neutron flux to optimize reactor power and fuel bum-up, and to provide excess reactivity needed to overcome xenon-135 poisoning following a reduction of power. The reactor is designed to develop full power output with all of the adjuster

Experimental evidence for cobalt(III)-carbene radicals: key intermediates in cobalt(II)-based metalloradical cyclopropanation

NARCIS (Netherlands)

Lu, H.; Dzik, W.I.; Xu, X.; Wojtas, L.; de Bruin, B.; Zhang, X.P.

2011-01-01

New and conclusive evidence has been obtained for the existence of cobalt(III)-carbene radicals that have been previously proposed as the key intermediates in the underlying mechanism of metalloradical cyclopropanation by cobalt(II) complexes of porphyrins. In the absence of olefin substrates,

Palladium-cobalt particles as oxygen-reduction electrocatalysts

Science.gov (United States)

Adzic, Radoslav [East Setauket, NY; Huang, Tao [Manorville, NY

2009-12-15

The present invention relates to palladium-cobalt particles useful as oxygen-reducing electrocatalysts. The invention also relates to oxygen-reducing cathodes and fuel cells containing these palladium-cobalt particles. The invention additionally relates to methods for the production of electrical energy by using the palladium-cobalt particles of the invention.

Removal of Cobalt Ions by Precipitate Foam Flotation

Energy Technology Data Exchange (ETDEWEB)

Jung, In Ha; Lee, Jung Won [Korea Atomic Energy Research Institute, Taejon (Korea)

1998-09-30

Simulated waste liquid containing 50 ppm cobalt ion was tested by precipitate flotation using a sodium lauryl sulfate as a collector. The effects of initial cobalt ion concentration, pH, surfactant concentration, flotation time, gas flow rate and foreign ions on removal efficiency of cobalt ion were studied. Pretreatment of the waste liquid with 35% H{sub 2}O{sub 2} prior to precipitate flotation made shift of optimal flotation pH from the strong alkalinity to weak alkaline range and made a favorable flotation of cobalt ion in wide range of pH. For the result of this experiment, 99.8% removal efficiency was obtained on the conditions of initial cobalt ion concentration 50 ppm, pH 9.5, gas flow rate 70 ml/min, flotation time 30 min. The simulate ion was formed to be the most harmful ion against removal of cobalt by precipitate flotation of the species which were tested. The presence of 0.1 M of SO{sub 4}{sup 2-} ion decreased removal efficiency of cobalt to 90% while the cobalt were almost entirely removed in the absence of sulfate ion. (author). 11 refs., 8 figs.

Synthesis and ammonolysis of nickel and cobalt tungstates and their characterisation

Directory of Open Access Journals (Sweden)

J.L. Rico

2016-07-01

Full Text Available The synthesis and characterization of NiW and CoW compounds are herein reported. The NiWO4 and CoWO4 samples, successfully synthesised by the hydrothermal method, were treated under NH3 to obtain the metal nitride. The SEM micrographs show that this transformation is a topotactic process. Tungsten trioxide was also treated under NH3 at similar operating conditions, and used as a reference. High nitrogen contents after ammonolysis were calculated, however, the percentages were below the theoretical values assuming the formation of pure NiWN, CoWN and WN. The XRD pattern indicates that WON is likely formed after ammonolysis of tungsten oxide whereas phase segregation was observed on the nickel and cobalt samples. Furthermore, the reactivity of the nitride samples as function of temperature was measured under argon and the results show that most of the nitrogen is removed from the cobalt and nickel samples whereas it was partially released from the tungsten specimen.

Spectral studies of coordination compounds of cobalt(II) with thiosemicarbazone of heterocyclic ketone

Science.gov (United States)

Chandra, Sulekh; Kumar, Umendra

2005-12-01

The paper presents the spectral analysis of cobalt(II) complexes with indoxyl thiosemicarbazone (ITSC) of general composition [CoL 2X 2] (where L = ITSC, X = Cl -, NO 3-, (1/2)SO 42-, NCS -). The geometry of the complexes have been characterized by elemental analysis, molar conductance, magnetic susceptibility measurements and spectral (electronic, IR, EPR, 1H NMR, mass) studies. The various physico-chemical techniques suggested a coordination number of six (octahedral) for chloro, nitrato and thiocyanato complexes. Whereas sulfato complex was found to have five coordinate trigonal-bipyramidal geometry. All the complexes are of high spin type showing magnetic moment corresponding to three unpaired electrons.

Cobalt Coordination and Clustering in α-Co(OH)2 Revealed by Synchrotron X-ray Total Scattering

International Nuclear Information System (INIS)

Neilson, James R.; Kurzman, Joshua A.; Seshadri, Ram; Morse, Daniel E.

2010-01-01

Structures of layered metal hydroxides are not well described by traditional crystallography. Total scattering from a synthesis-controlled subset of these materials, as described here, reveals that different cobalt coordination polyhedra cluster within each layer on short length scales, offering new insights and approaches for understanding the properties of these and related layered materials. Structures related to that of brucite (Mg(OH) 2 ) are ubiquitous in the mineral world and offer a variety of useful functions ranging from catalysis and ion-exchange to sequestration and energy transduction, including applications in batteries. However, it has been difficult to resolve the atomic structure of these layered compounds because interlayer disorder disrupts the long-range periodicity necessary for diffraction-based structure determination. For this reason, traditional unit-cell-based descriptions have remained inaccurate. Here we apply, for the first time to such layered hydroxides, synchrotron X-ray total scattering methods - analyzing both the Bragg and diffuse components - to resolve the intralayer structure of three different α-cobalt hydroxides, revealing the nature and distribution of metal site coordination. The different compounds with incorporated chloride ions have been prepared with kinetic control of hydrolysis to yield different ratios of octahedrally and tetrahedrally coordinated cobalt ions within the layers, as confirmed by total scattering. Real-space analyses indicate local clustering of polyhedra within the layers, manifested in the weighted average of different ordered phases with fixed fractions of tetrahedrally coordinated cobalt sites. These results, hidden from an averaged unit-cell description, reveal new structural characteristics that are essential to understanding the origin of fundamental material properties such as color, anion exchange capacity, and magnetic behavior. Our results also provide further insights into the detailed

Cobalt coordination and clustering in alpha-Co(OH)(2) revealed by synchrotron X-ray total scattering.

Science.gov (United States)

Neilson, James R; Kurzman, Joshua A; Seshadri, Ram; Morse, Daniel E

2010-09-03

Structures of layered metal hydroxides are not well described by traditional crystallography. Total scattering from a synthesis-controlled subset of these materials, as described here, reveals that different cobalt coordination polyhedra cluster within each layer on short length scales, offering new insights and approaches for understanding the properties of these and related layered materials. Structures related to that of brucite [Mg(OH)(2)] are ubiquitous in the mineral world and offer a variety of useful functions ranging from catalysis and ion-exchange to sequestration and energy transduction, including applications in batteries. However, it has been difficult to resolve the atomic structure of these layered compounds because interlayer disorder disrupts the long-range periodicity necessary for diffraction-based structure determination. For this reason, traditional unit-cell-based descriptions have remained inaccurate. Here we apply, for the first time to such layered hydroxides, synchrotron X-ray total scattering methods-analyzing both the Bragg and diffuse components-to resolve the intralayer structure of three different alpha-cobalt hydroxides, revealing the nature and distribution of metal site coordination. The different compounds with incorporated chloride ions have been prepared with kinetic control of hydrolysis to yield different ratios of octahedrally and tetrahedrally coordinated cobalt ions within the layers, as confirmed by total scattering. Real-space analyses indicate local clustering of polyhedra within the layers, manifested in the weighted average of different ordered phases with fixed fractions of tetrahedrally coordinated cobalt sites. These results, hidden from an averaged unit-cell description, reveal new structural characteristics that are essential to understanding the origin of fundamental material properties such as color, anion exchange capacity, and magnetic behavior. Our results also provide further insights into the detailed

Cobalt: for strength and color

Science.gov (United States)

Boland, Maeve A.; Kropschot, S.J.

2011-01-01

Cobalt is a shiny, gray, brittle metal that is best known for creating an intense blue color in glass and paints. It is frequently used in the manufacture of rechargeable batteries and to create alloys that maintain their strength at high temperatures. It is also one of the essential trace elements (or "micronutrients") that humans and many other living creatures require for good health. Cobalt is an important component in many aerospace, defense, and medical applications and is a key element in many clean energy technologies. The name cobalt comes from the German word kobold, meaning goblin. It was given this name by medieval miners who believed that troublesome goblins replaced the valuable metals in their ore with a substance that emitted poisonous fumes when smelted. The Swedish chemist Georg Brandt isolated metallic cobalt-the first new metal to be discovered since ancient times-in about 1735 and identified some of its valuable properties.

Effects of cobalt in nickel-base superalloys

Science.gov (United States)

Tien, J. K.; Jarrett, R. N.

1983-01-01

The role of cobalt in a representative wrought nickel-base superalloy was determined. The results show cobalt affecting the solubility of elements in the gamma matrix, resulting in enhanced gamma' volume fraction, in the stabilization of MC-type carbides, and in the stabilization of sigma phase. In the particular alloy studied, these microstructural and microchemistry changes are insufficient in extent to impact on tensile strength, yield strength, and in the ductilities. Depending on the heat treatment, creep and stress rupture resistance can be cobalt sensitive. In the coarse grain, fully solutioned and aged condition, all of the alloy's 17% cobalt can be replaced by nickel without deleteriously affecting this resistance. In the fine grain, partially solutioned and aged condition, this resistance is deleteriously affected only when one-half or more of the initial cobalt content is removed. The structure and property results are discussed with respect to existing theories and with respect to other recent and earlier findings on the impact of cobalt, if any, on the performance of nickel-base superalloys.

Cobalt: A vital element in the aircraft engine industry

Science.gov (United States)

Stephens, J. R.

1981-01-01

Recent trends in the United States consumption of cobalt indicate that superalloys for aircraft engine manufacture require increasing amounts of this strategic element. Superalloys consume a lion's share of total U.S. cobalt usage which was about 16 million pounds in 1980. In excess of 90 percent of the cobalt used in this country was imported, principally from the African countries of Zaire and Zambia. Early studies on the roles of cobalt as an alloying element in high temperature alloys concentrated on the simple Ni-Cr and Nimonic alloy series. The role of cobalt in current complex nickel base superalloys is not well defined and indeed, the need for the high concentration of cobalt in widely used nickel base superalloys is not firmly established. The current cobalt situation is reviewed as it applies to superalloys and the opportunities for research to reduce the consumption of cobalt in the aircraft engine industry are described.

Feasibility Study for Cobalt Bundle Loading to CANDU Reactor Core

International Nuclear Information System (INIS)

Park, Donghwan; Kim, Youngae; Kim, Sungmin

2016-01-01

CANDU units are generally used to produce cobalt-60 at Bruce and Point Lepreau in Canada and Embalse in Argentina. China has started production of cobalt-60 using its CANDU 6 Qinshan Phase III nuclear power plant in 2009. For cobalt-60 production, the reactor’s full complement of stainless steel adjusters is replaced with neutronically equivalent cobalt-59 adjusters, which are essentially invisible to reactor operation. With its very high neutron flux and optimized fuel burn-up, the CANDU has a very high cobalt-60 production rate in a relatively short time. This makes CANDU an excellent vehicle for bulk cobalt-60 production. Several studies have been performed to produce cobalt-60 using adjuster rod at Wolsong nuclear power plant. This study proposed new concept for producing cobalt-60 and performed the feasibility study. Bundle typed cobalt loading concept is proposed and evaluated the feasibility to fuel management without physics and system design change. The requirement to load cobalt bundle to the core was considered and several channels are nominated. The production of cobalt-60 source is very depend on the flux level and burnup directly. But the neutron absorption characteristic of cobalt bundle is too high, so optimizing design study is needed in the future

Feasibility Study for Cobalt Bundle Loading to CANDU Reactor Core

Energy Technology Data Exchange (ETDEWEB)

Park, Donghwan; Kim, Youngae; Kim, Sungmin [KHNP Central Research Institute, Daejeon (Korea, Republic of)

2016-10-15

CANDU units are generally used to produce cobalt-60 at Bruce and Point Lepreau in Canada and Embalse in Argentina. China has started production of cobalt-60 using its CANDU 6 Qinshan Phase III nuclear power plant in 2009. For cobalt-60 production, the reactor’s full complement of stainless steel adjusters is replaced with neutronically equivalent cobalt-59 adjusters, which are essentially invisible to reactor operation. With its very high neutron flux and optimized fuel burn-up, the CANDU has a very high cobalt-60 production rate in a relatively short time. This makes CANDU an excellent vehicle for bulk cobalt-60 production. Several studies have been performed to produce cobalt-60 using adjuster rod at Wolsong nuclear power plant. This study proposed new concept for producing cobalt-60 and performed the feasibility study. Bundle typed cobalt loading concept is proposed and evaluated the feasibility to fuel management without physics and system design change. The requirement to load cobalt bundle to the core was considered and several channels are nominated. The production of cobalt-60 source is very depend on the flux level and burnup directly. But the neutron absorption characteristic of cobalt bundle is too high, so optimizing design study is needed in the future.

Nickel, cobalt, and their alloys

CERN Document Server

2000-01-01

This book is a comprehensive guide to the compositions, properties, processing, performance, and applications of nickel, cobalt, and their alloys. It includes all of the essential information contained in the ASM Handbook series, as well as new or updated coverage in many areas in the nickel, cobalt, and related industries.

Cobalt sorption onto Savannah River Plant soils

International Nuclear Information System (INIS)

Hoeffner, S.L.

1985-06-01

A laboratory study of cobalt-60 sorption was conducted using Savannah River Plant soil and groundwater from the low-level waste burial ground. Systematic variation of soil and water composition indicates that cobalt sorption is most strongly a function of pH. Over a pH range of 2 to 9, the distribution coefficient ranged from 2 to more than 10,000 mL/g. Changes in clay content and in K + , Ca 2+ , or Mg 2+ concentrations influence cobalt sorption indirectly through the slight pH changes which result. The ions Na + , Cl - , and NO 3 - have no effect on cobalt sorption. Ferrous ion, added to groundwater to simulate the condition of water at the bottom of the waste trenches, accounts for part of the decrease in cobalt sorption observed with trench waters. 17 refs., 3 figs., 4 tabs

Genotoxicity of two heavy metal compounds: lead nitrate and cobalt chloride in Polychaete Perinereis cultrifera.

Science.gov (United States)

Singh, Nisha; Bhagat, Jacky; Ingole, Baban S

2017-07-01

The present study explores the in vivo and in vitro genotoxic effects of lead nitrate, [Pb(NO 3 ) 2 ] a recognized environmental pollutant and cobalt chloride (CoCl 2 ), an emerging environmental pollutant in polychaete Perinereis cultrifera using comet assay. Despite widespread occurrence and extensive industrial applications, no previous published reports on genotoxicity of these compounds are available in polychaete as detected by comet assay. Polychaetes were exposed in vivo to Pb(NO 3 ) 2 (0, 100, 500, and 1000 μg/l) and CoCl 2 (0, 100, 300, and 500 μg/l) for 5 days. At 100 μg/l Pb(NO 3 ) 2 concentration, tail DNA (TDNA) values in coelomocytes were increase by 1.16, 1.43, and 1.55-fold after day 1, day 3, and day 5, whereas, OTM showed 1.12, 2.33, and 2.10-fold increase in in vivo. Pb(NO 3 ) 2 showed a concentration and time-dependent genotoxicity whereas CoCl 2 showed a concentration-dependent genotoxicity in in vivo. A concentration-dependent increase in DNA damage was observed in in vitro studies for Pb(NO 3 ) 2 and CoCl 2 . DNA damage at 500 μg/L showed almost threefold increase in TDNA and approximately fourfold increase in OTM as compared to control in in vitro. Our studies suggest that Pb(NO 3 ) 2 and CoCl 2 have potential to cause genotoxic damage, with Pb(NO 3 ) 2 being more genotoxic in polychaete and should be used more carefully in industrial and other activities. Graphical abstract.

Manipulating radicals: Using cobalt to steer radical reactions

OpenAIRE

Chirilă, A.

2017-01-01

This thesis describes research aimed at understanding and exploiting metallo-radical reactivity and explores reactions mediated by square planar, low-spin cobalt(II) complexes. A primary goal was to uncover novel reactivity of discrete cobalt(III)-bound carbene radicals generated upon reaction of the cobalt(II) catalysts with carbene precursors. Another important goal was to replace cobalt(II)-porphyrin catalysts with cheaper and easier to prepare metallo-radical analogues. Therefore the cata...

Efficient hydrogen evolution catalysis using ternary pyrite-type cobalt phosphosulphide

KAUST Repository

Cabán-Acevedo, Miguel

2015-09-14

The scalable and sustainable production of hydrogen fuel through water splitting demands efficient and robust Earth-abundant catalysts for the hydrogen evolution reaction (HER). Building on promising metal compounds with high HER catalytic activity, such as pyrite structure cobalt disulphide (CoS 2), and substituting non-metal elements to tune the hydrogen adsorption free energy could lead to further improvements in catalytic activity. Here we present a combined theoretical and experimental study to establish ternary pyrite-type cobalt phosphosulphide (CoPS) as a high-performance Earth-abundant catalyst for electrochemical and photoelectrochemical hydrogen production. Nanostructured CoPS electrodes achieved a geometrical catalytic current density of 10 mA cm at overpotentials as low as 48mV, with outstanding long-term operational stability. Integrated photocathodes of CoPS on n -p-p silicon micropyramids achieved photocurrents up to 35 mA cm at 0 V versus the reversible hydrogen electrode (RHE), onset photovoltages as high as 450 mV versus RHE, and the most efficient solar-driven hydrogen generation from Earth-abundant systems.

Transport of cobalt-60 industrial radiation sources

Science.gov (United States)

Kunstadt, Peter; Gibson, Wayne

This paper will deal with safety aspects of the handling of Cobalt-60, the most widely used industrial radio-isotope. Cobalt-60 is a man-made radioisotope of Cobalt-59, a naturally occurring non radioactive element, that is made to order for radiation therapy and a wide range of industrial processing applications including sterilization of medical disposables, food irradiation, etc.

The physiological effect of cobalt on watermelon cultivation

International Nuclear Information System (INIS)

Yao Naihua; Jin Yafang; Sun Yaochen; Huang Yiming

1993-01-01

Cobalt has essential physiological action on both animals and plants. For the latter it can raise plant's nitrogen-fixing ability and saccharine content. Spray of cobalt mixed with other nutritive elements can improve the germinatit of seeds and the yield of fruit. For specifying the nutritive function of cobalt upon watermelon, isotope 60 Co was mixed into a complex leaf nutritive aqua and the regularity of transferring and absorbing cobalt in the watermelon's body was investigated

Relaxation resistance of heat resisting alloys with cobalt

International Nuclear Information System (INIS)

Borzdyka, A.M.

1977-01-01

Relaxation resistance of refractory nickel-chromium alloys containing 5 to 14 % cobalt is under study. The tests involve the use of circular samples at 800 deg to 850 deg C. It is shown that an alloy containing 14% cobalt possesses the best relaxation resistance exceeding that of nickel-chromium alloys without any cobalt by a factor of 1.5 to 2. The relaxation resistance of an alloy with 5% cobalt can be increased by hardening at repeated loading

Heating-induced inner-sphere substitution and reduction-oxidation reactions of the solid phenanthroline containing cobalt (2) and cobalt (3) complexes

International Nuclear Information System (INIS)

Palade, D.M.

1996-01-01

The results of the differential thermal and thermogravimetric analyses of solid phenanthroline-containing complexes of cobalt (2) and cobalt (3) in the atmosphere of the air have been analyzed. Mechanism of redox reactions occurring when cobalt (3) complexes are heated has been discussed. It is shown that some of gaseous products of the redox processes appear as a result of secondary reactions and not the processes of the ligands oxidation by Co 3+ . The influence of certain inner-sphere and coordinated anions (of I, inclusively) on cobalt (3) complexes behaviour during heating has been considered

Two dimensionality in quasi-one-dimensional cobalt oxides confirmed by muon-spin spectroscopy

International Nuclear Information System (INIS)

Sugiyama, J.; Nozaki, H.; Ikedo, Y.; Mukai, K.; Andreica, D.; Amato, A.; Brewer, J.H.; Ansaldo, E.J.; Morris, G.D.; Takami, T.; Ikuta, H.

2007-01-01

The quasi-one-dimensional (Q1D) cobalt oxides, A n+2 Co n+1 O 3n+3 (A=Ca, Sr and Ba, n=1-∼), were investigated by muon-spin spectroscopy under applied pressures of up to 1.1GPa. The relationship between the onset Neel temperature T N on and the inter-chain distance (d ic ), which increases monotonically with n, is well fitted by the formula T N /T N,0 =(1-d ic /d ic,0 ) β . The T N on -d ic curve also predicts a large P dependence of T N for the compounds with n>=5, i.e., in the vicinity of d ic,0 , while the n=1-4 compounds show only a very small effect. Indeed, our high-pressure μ + SR results show that T N of BaCoO 3 (n=∼) is enhanced by P, with a slope of 2.1 K/GPa, whereas no detectable changes between ambient pressure and 1.0 GPa for both Ca 3 Co 2 O 6 (n=1) and Sr 4 Co 3 O 9 (n=2). This clearly confirms the role of the 2D-AF interaction on T N on in the Q1D cobalt oxides

Control of carbon nanotube growth using cobalt nanoparticles as catalyst

International Nuclear Information System (INIS)

Huh, Yoon; Green, Malcolm L.H.; Kim, Young Heon; Lee, Jeong Yong; Lee, Cheol Jin

2005-01-01

We have controllably grown carbon nanotubes using uniformly distributed cobalt nanoparticles as catalyst. Cobalt nanoparticles with a uniform size were synthesized by chemical reaction and colloidal solutions including the cobalt nanoparticles were prepared. The cobalt nanoparticles were uniformly distributed on silicon substrates by a spin-coating method. Carbon nanotubes with a uniform diameter were synthesized on the cobalt nanoparticles by thermal chemical vapor deposition of acetylene gas. The density and vertical alignment of carbon nanotubes could be controlled by adjusting the density of cobalt (Co) nanoparticles

Dosing of anaerobic granular sludge bioreactors with cobalt: Impact of cobalt retention on methanogenic activity

KAUST Repository

Fermoso, Fernando G.

2010-12-01

The effect of dosing a metal limited anaerobic sludge blanket (UASB) reactor with a metal pulse on the methanogenic activity of granular sludge has thus far not been successfully modeled. The prediction of this effect is crucial in order to optimize the strategy for metal dosage and to prevent unnecessary losses of resources. This paper describes the relation between the initial immobilization of cobalt in anaerobic granular sludge cobalt dosage into the reactor and the evolution of methanogenic activity during the subsequent weeks. An operationally defined parameter (A0· B0) was found to combine the amount of cobalt immobilized instantaneously upon the pulse (B0) and the amount of cobalt immobilized within the subsequent 24. h (A0). In contrast with the individual parameters A0 and B0, the parameter A0· B0 correlated significantly with the methanogenic activity of the sludge during the subsequent 16 or 35. days. This correlation between metal retention and activity evolution is a useful tool to implement trace metal dosing strategies for biofilm-based biotechnological processes. © 2010.

Operationally defined species characterization and bioaccessibility evaluation of cobalt, copper and selenium in Cape gooseberry (Physalis Peruviana L.) by SEC-ICP MS.

Science.gov (United States)

Wojcieszek, Justyna; Ruzik, Lena

2016-03-01

Physalis peruviana could attract great interest because of its nutritional and industrial properties. It is an excellent source of vitamins, minerals, essential fatty acids and carotenoids. Physalis Peruviana is also known to have a positive impact on human health. Unfortunately, still little is known about trace elements present in Physalis Peruviana and their forms available for the human body. Thus, the aim of this study was to estimate bioaccessibility and characterization of species of cobalt, copper and selenium in Physalis Peruviana fruits. Total and extractable contents of elements were determined by mass spectrometer with inductively coupled plasma (ICP MS). In order to separate the different types of metal complexes Physalis peruviana fruits were treated with the following solvents: Tris-HCl (pH 7.4), sodium dodecyl sulfate (SDS) (pH 7.4) and ammonium acetate (pH 5.5). The best efficiency of extraction of: cobalt was obtained for ammonium acetate (56%) and Tris-HCl (60%); for copper was obtained for SDS (66%), for selenium the best extraction efficiency was obtained after extraction with SDS (48%). To obtain information about bioaccessibility of investigated elements, enzymatic extraction based on in vitro simulation of gastric (pepsin) and intestinal (pancreatin) digestion was performed. For copper and selenium the simulation of gastric digestion leads to the extraction yield above 90%, while both steps of digestion method were necessary to obtain satisfactory extraction yield in the case of cobalt. Size exclusion chromatography (SEC) coupled to on-line ICP MS detection was used to investigate collected metal species. The main fraction of metal compounds was found in the 17 kDa region. Cobalt and copper create complexes mostly with compounds extracted by means of ammonium acetate and SDS, respectively. Cobalt, copper and selenium were found to be highly bioaccessible from Physalis Peruviana. Investigation of available standards of cobalt and selenium

Low-Temperature Thermoelectric Properties of Fe2VAl with Partial Cobalt Doping

Science.gov (United States)

Liu, Chang; Morelli, Donald T.

2012-06-01

Ternary metallic alloy Fe2VAl with a pseudogap in its energy band structure has received intensive scrutiny for potential thermoelectric applications. Due to the sharp change in the density of states profile near the Fermi level, interesting transport properties can be triggered to render possible enhancement in the overall thermoelectric performance. Previously, this full-Heusler-type alloy was partially doped with cobalt at the iron sites to produce a series of compounds with n-type conductivity. Their thermoelectric properties in the temperature range of 300 K to 850 K were reported. In this research, efforts were made to extend the investigation on (Fe1- x Co x )2VAl to the low-temperature range. Alloy samples were prepared by arc-melting and annealing. Seebeck coefficient, electrical resistivity, and thermal conductivity measurements were performed from 80 K to room temperature. The effects of cobalt doping on the material's electronic and thermal properties are discussed.

Cobalt-60 control in Ontario Hydro reactors

International Nuclear Information System (INIS)

Lacy, C.S.

1988-01-01

This paper discusses the impact of specifying reduced Cobalt-59 in the primary heat transport circuit materials of construction on the radiation fields developed around the primary circuit. An eight-fold reduction in steam generator radiation fields due to Cobalt-60 has been observed for two identical sets of reactors, one with and one without Cobalt-59 control. The comparison is between eight reactors at the Pickering Nuclear Generating Station (PNGS). Units 5 to 8 (PNGS-B) are identical to Units 1 to 4 (PNGS-A) except that PNGS-B has reduced impurity Cobalt-59 in the alloys of construction and a reduced use of stellite. The effects of chemistry control are also discussed

Cobalt-related features of spectral and magnetic properties of RNi4Co (R=Ho, Er)

International Nuclear Information System (INIS)

Lukoyanov, A.V.; Knyazev, Yu.V.; Kuz‘min, Yu.I.; Kuchin, A.G.

2014-01-01

In this paper we investigate spectral and magnetic properties of RNi 4 Co (R=Ho, Er) intermetallics to reveal the features associated with the presence of Co substituting ion in comparison with the parent HoNi 5 and ErNi 5 compounds. Our ab initio LSDA+U calculations show that in the electronic structure Co states are strongly manifested near the Fermi energy for the case of Co in 2c position, while Co in 3g position results only in weak changes of the total DOS curve. Theoretical optical conductivity calculated assuming Co equally redistributed among 2c or 3g positions agrees well with the experimental optical conductivity. Cobalt ion in RNi 4 Co (R=Ho, Er) is characterized by magnetic moment of 1μ B that increases exchange interaction in the 3d sublattice by several times that contributes to the growth of Curie temperature in comparison with the parent compounds. - Highlights: • Electronic structure of RNi4Co (R=Ho, Er) is calculated in LSDA+U. • Cobalt ion is considered in 2c or 3g position and compared. • Experimental optical conductivity is interpreted based on the calculated one

An elevator for cobalt-60 source

International Nuclear Information System (INIS)

Tang Zaimin; Liang Donghu

1990-07-01

The elevator used for cobalt-60 source is a key device in the irradiation industry. It plays an important role in the safety and control of irradiation operation as well as the utilization rate of radiation source. From 1983 to 1986, Beijing Institute of Nuclear Engineering undertook designing of various size irradiation projects for different uses. Since then a kind of cobalt-60 source elevator suited for the irradiator of wet-source-storage has been chosen. It is reliable in the operation and complete in the function. An automatic control circuit brings the systems of cobalt-60 source elevator into an interlock system which ensures the irradiation operation safety. Besides introducing the structural features and performance of this elevator, the conditions of safety interlocking in raising or lowering the cobalt-60 source is also discussed. The discussion is from the safety viewpoint of operating an irradiator and irradiation technology

SYNTHESIS AND ANTITUMOR ACTIVITY OF COPPER, NICKEL AND COBALT COORDINATION COMPOUNDS WITH 1-(2-HYDROXYPHENYLETHANONE N(4-ALLYL-3-THIOSEMICARBAZONE

Directory of Open Access Journals (Sweden)

Vasilii GRAUR

2015-12-01

Full Text Available The paper presents the synthesis of the ligand 1-(2-hydroxyphenylethanone N(4-allyl-3-thiosemicarbazone (H2L and six coordination compounds of copper, nickel and cobalt with this ligand. The structure of thiosemicarbazone H2L was studied using 1H and 13С NMR spectroscopy. The synthesized coordination compounds were studied using elemental analysis, gravimetric analysis of water content, molar conductivity, and magnetochemistry. For H2L the antitumor activity towards human leukemia HL-60 cells and cervical cancer HeLa cells was determined. It was established that the substitution of hydrogen atom with methyl group in the azomethinic fragment leads to the growth of antitumor activity.SINTEZA ŞI ACTIVITATEA ANTITUMORALĂ A COMPUŞILOR COMPLECŞI AI CUPRULUI, NICHELULUI ŞI COBALTULUI CU N(4-ALIL-3-TIOSEMICARBAZONA 1-(2-HIDROXIFENILETANONEILucrarea conţine descrierea sintezei N(4-alil-3-tiosemicarbazonei 1-(2-hidroxifeniletanonei (H2L şi a şase compuşi coordinativi ai cuprului, nichelului şi cobaltului cu acest ligand. Structura tiosemicarbazonei H2L a fost stabilită în baza datelor spectroscopiei RMN 1H şi 13C. Compuşi coordinativi au fost studiaţi cu ajutorul analizei elementale, analizei gravimetrice a conţinutului de apă, conductivitaţii molare şi magnetochimiei. Pentru H2L a fost determinată activitatea antitumorală faţă de celulele leucemiei umane HL-60 şi ale cancerului cervical HeLa. S-a stabilit că înlocuirea atomului de hidrogen cu o grupare metil în fragmentul azomethinic conduce la creşterea activitaţii antitumorale.

Cobalt rare earth permanent magnets (citations from the Engineering Index data base). Final report for 1970--May 1978

International Nuclear Information System (INIS)

Smith, M.F.

1978-06-01

Research summaries from worldwide journals on fabrication, composition, bonding, sintering, pressing, and processing of these magnets are presented. Studies on phase transformations, microstructure, intermetallic compounds, and anisotropy are covered. The efficiency of electric motors, traveling wave tubes, microwave equipment and magnetic tape drives using cobalt rare earth magnets is included

JAEA thermodynamic database for performance assessment of geological disposal of high-level and TRU wastes. Selection of thermodynamic data of cobalt and nickel

International Nuclear Information System (INIS)

Kitamura, Akira; Yui, Mikazu; Kirishima, Akira; Saito, Takumi; Shibutani, Sanae; Tochiyama, Osamu

2009-11-01

Within the scope of the JAEA thermodynamic database project for performance assessment of geological disposal of high-level and TRU wastes, the selection of the thermodynamic data on the inorganic compounds and complexes of cobalt and nickel have been carried out. For cobalt, extensive literature survey has been performed and all the obtained literatures have been carefully reviewed to select the thermodynamic data. Selection of thermodynamic data of nickel has been based on a thermodynamic database published by the Nuclear Energy Agency in the Organisation for Economic Co-operation and Development (OECD/NEA), which has been carefully reviewed by the authors, and then thermodynamic data have been selected after surveying latest literatures. Based on the similarity of chemical properties between cobalt and nickel, complementary thermodynamic data of nickel and cobalt species expected under the geological disposal condition have been selected to complete the thermodynamic data set for the performance assessment of geological disposal of radioactive wastes. (author)

21 CFR 73.1015 - Chromium-cobalt-aluminum oxide.

Science.gov (United States)

2010-04-01

... 21 Food and Drugs 1 2010-04-01 2010-04-01 false Chromium-cobalt-aluminum oxide. 73.1015 Section 73... LISTING OF COLOR ADDITIVES EXEMPT FROM CERTIFICATION Drugs § 73.1015 Chromium-cobalt-aluminum oxide. (a) Identity. The color additive chromium-cobalt-aluminum oxide is a blue-green pigment obtained by calcining a...

Studies of the yields of 57Fe(II)-species produced after the EC-decay and of 60Co(II)-species produced in the (n, γ) reaction in cobalt(III) coordination compounds

International Nuclear Information System (INIS)

Sano, Hirotoshi; Harada, Masayuki; Endo, Kazutoyo

1978-01-01

The yields of 57 Fe(II)-species produced after EC-decay were compared with those of 60 Co(II)-species produced in the 59 Co(n, γ) 60 Co reaction for twelve cobalt(III) coordination compounds. The results indicate that the radiochemical yield of 60 Co(II)-species correlates with the yield of 57 Fe(II)-species except in the case of [Co(NH 3 ) 6 ] 2 (CrO 4 ) 3 . The anomalously low yield of 57 Fe(II)-species in [Co(NH 3 ) 6 ] 2 (CrO 4 ) 3 is ascribed to the reaction of chromate anions with ammine ligands initiated by the nuclear transformation in a solid. (author)

Effects of nickel and cobalt addition on creep strength and microstructure of the precipitation-strengthened 15Cr ferritic steels

Energy Technology Data Exchange (ETDEWEB)

Shibuya, Masachika; Toda, Yoshiaki; Sawada, Kota; Kushima, Hideaki; Kimura, Kazuhiro [National Inst. for Materials Science, Tsukuba, Ibaraki (Japan)

2010-07-01

Creep strength of 15Cr ferritic steel with ferrite matrix was increased by precipitation strengthening of intermetallic compounds. It was higher than those of 9-12Cr ferritic steels with a tempered martensitic microstructure strengthened by carbide and carbonitride. Addition of nickel was confirmed to improve Charpy impact toughness of the 15Cr steels, however, creep strength was slightly reduced by the addition of nickel. Microstructure of the 15Cr steel changes from ferrite single phase to dual phases of ferrite and martensite with the addition of nickel which is an austenite stabilizing element. The 15Cr steels investigated in the previous study, contain 3mass% of cobalt which is also an austenite stabilizing element, therefore, the influence of nickel and cobalt combination on mechanical properties and microstructure of the 15Cr-1Mo-6W-V-Nb steel is investigated in this study. Creep strength, Charpy impact toughness and microstructure of the steel were strongly influenced by the composition of nickel and cobalt. Design guideline of the 15Cr steel is discussed with respect to a role of microstructure and combination of nickel and cobalt addition. (orig.)

Cobalt release from inexpensive jewellery: has the use of cobalt replaced nickel following regulatory intervention?

DEFF Research Database (Denmark)

Thyssen, Jacob Pontoppidan; Jellesen, Morten S; Menné, Torkil

2010-01-01

Before the introduction of the EU Nickel Directive, concern was raised that manufacturers of jewellery might turn from the use of nickel to cobalt following the regulatory intervention on nickel exposure.......Before the introduction of the EU Nickel Directive, concern was raised that manufacturers of jewellery might turn from the use of nickel to cobalt following the regulatory intervention on nickel exposure....

The role of cobalt on the creep of Waspaloy

Science.gov (United States)

Jarrett, R. N.; Chin, L.; Tien, J. K.

1984-01-01

Cobalt was systematically replaced with nickel in Waspaloy (which normally contains 13% Co) to determine the effects of cobalt on the creep behavior of this alloy. Effects of cobalt were found to be minimal on tensile strengths and microstructure. The creep resistance and the stress rupture resistance determined in the range from 704 to 760 C (1300 to 1400 C) were found to decrease as cobalt was removed from the standard alloy at all stresses and temperatures. Roughly a ten-fold drop in rupture life and a corresponding increase in minimum creep rate were found under all test conditions. Both the apparent creep activation energy and the matrix contribution to creep resistance were found to increase with cobalt. These creep effects are attributed to cobalt lowering the stacking fault energy of the alloy matrix. The creep resistance loss due to the removal of cobalt is shown to be restored by slightly increasing the gamma' volume fraction. Results are compared to a previous study on Udimet 700, a higher strength, higher gamma' volume fraction alloy with similar phase chemistry, in which cobalt did not affect creep resistance. An explanation for this difference in behavior based on interparticle spacing and cross-slip is presented.

Nickel-cobalt hydroxide nanosheets: Synthesis, morphology and electrochemical properties.

Science.gov (United States)

Schneiderová, Barbora; Demel, Jan; Zhigunov, Alexander; Bohuslav, Jan; Tarábková, Hana; Janda, Pavel; Lang, Kamil

2017-08-01

This paper reports the synthesis, characterization, and electrochemical performance of nickel-cobalt hydroxide nanosheets. The hydroxide nanosheets of approximately 0.7nm thickness were prepared by delamination of layered nickel-cobalt hydroxide lactate in water and formed transparent colloids that were stable for months. The nanosheets were deposited on highly oriented pyrolytic graphite by spin coating, and their electrochemical behavior was investigated by cyclic voltammetry in potassium hydroxide electrolyte. Our method of electrode preparation allows for studying the electrochemistry of nanosheets where the majority of the active centers can participate in the charge transfer reaction. The observed electrochemical response was ascribed to mutual compensation of the cobalt and nickel response via electron sharing between these metals in the hydroxide nanosheets, a process that differentiates the behavior of nickel-cobalt hydroxide nanosheets from single nickel hydroxide or cobalt hydroxide nanosheets or their physical mixture. The presence of cobalt in the nickel-cobalt hydroxide nanosheets apparently decreases the time of electrochemical activation of the nanosheet layer, which for the nickel hydroxide nanosheets alone requires more potential sweeps. Copyright © 2017 Elsevier Inc. All rights reserved.

Thin film Heusler compounds manganese nickel gallium

Science.gov (United States)

Jenkins, Catherine Ann

Multiferroic Heusler compounds Mn3--xNi xGa (x=0,1,2) have a tetragonal unit cell that can variously be used for magneto-mechanically coupled shape memory ( x=1,2) and spin-mechanical applications (x=0). The first fabrication of fully epitaxial thin films of these and electronically related compounds by sputtering is discussed. Traditional and custom lab characterization of the magnetic and temperature driven multiferroic behavior is augmented by more detailed synchrotron-based high energy photoemission spectroscopic techniques to describe the atomic and electronic structure. Integration of the MnNi2Ga magnetic shape memory compound in microwave patch antennas and active free-standing structures represents a fraction of the available and promising applications for these compounds. Prototype magnetic tunnel junctions are demonstrated by Mn3Ga electrodes with perpendicular anisotropy for spin torque transfer memory structures. The main body of the work concentrates on the definition and exploration of the material series Mn3--xNi xGa (x=0,1,2) and the relevant multiferroic phenomena exhibited as a function of preparation and external stimuli. Engineering results on each x=0,1,2 are presented with device prototypes where relevant. In the appendices the process of the materials design undertaken with the goal of developing new ternary intermetallics with enhanced properties is presented with a full exploration of the road from band structure calculations to device implementation. Cobalt based compounds in single crystal and nanoparticle form are fabricated with an eye to developing the production methods for new cobalt- and iron-based magnetic shape memory compounds for device applications in different forms. Mn2CoSn, a compound isolectronic and with similar atomic ordering to Mn2NiGa is experimentally determined to be a nearly half-metallic ferromagnet in contrast to the metallic ferrimagnetism in the parent compound. High energy photoemission spectroscopy is shown to

A Novel Coordination Polymer Based on Trinuclear Cobalt Building Blocks Cluster: Synthesis, Crystal Structure, and Properties

Science.gov (United States)

Lu, J. F.; Tang, Z. H.; Shi, J.; Ge, H. G.; Jiang, M.; Song, J.; Jin, L. X.

2017-12-01

The title compound {[Co3(μ3-OH)(μ2-H2O)2(H2O)5(BTC)2] · 6H2O} n (H3BTC is a 1,3,5-benzenetricarboxylic acid) was prepared and characterized by single crystal and powder X-ray diffraction, Fourier transform infrared spectroscopy, thermogravimetric and elemental analyses. The single crystal X-ray diffraction reveals that the title compound consists of 1D infinite zigzag chains which were constructed by trinuclear cobalt cluster and BTC3- ligand. Neighbouring above-mentioned 1D infinite zigzag chains are further linked by intermolecular hydrogen bonding to form a 3D supermolecular structure. In addition, the luminescent properties of the title compound were investigated.

Stable and Inert Cobalt Catalysts for Highly Selective and Practical Hydrogenation of C≡N and C═O Bonds.

Science.gov (United States)

Chen, Feng; Topf, Christoph; Radnik, Jörg; Kreyenschulte, Carsten; Lund, Henrik; Schneider, Matthias; Surkus, Annette-Enrica; He, Lin; Junge, Kathrin; Beller, Matthias

2016-07-20

Novel heterogeneous cobalt-based catalysts have been prepared by pyrolysis of cobalt complexes with nitrogen ligands on different inorganic supports. The activity and selectivity of the resulting materials in the hydrogenation of nitriles and carbonyl compounds is strongly influenced by the modification of the support and the nitrogen-containing ligand. The optimal catalyst system ([Co(OAc)2/Phen@α-Al2O3]-800 = Cat. E) allows for efficient reduction of both aromatic and aliphatic nitriles including industrially relevant dinitriles to primary amines under mild conditions. The generality and practicability of this system is further demonstrated in the hydrogenation of diverse aliphatic, aromatic, and heterocyclic ketones as well as aldehydes, which are readily reduced to the corresponding alcohols.

Characterization of a Porous Carbon Material Functionalized with Cobalt-Oxide/Cobalt Core-Shell Nanoparticles for Lithium Ion Battery Electrodes

KAUST Repository

Anjum, Dalaver H.; Rasul, Shahid; Roldan-Gutierrez, Manuel A.; Da Costa, Pedro M. F. J.

2016-01-01

A nanoporous carbon (C) material, functionalized with Cobalt-Oxide/Cobalt (CoO/Co) core-shell nanoparticles (NPs), was structurally and chemically characterized with transmission electron microcopy (TEM) while its electrochemical response

Cobalt mineral exploration and supply from 1995 through 2013

Science.gov (United States)

Wilburn, David R.

2011-01-01

The global mining industry has invested a large amount of capital in mineral exploration and development over the past 15 years in an effort to ensure that sufficient resources are available to meet future increases in demand for minerals. Exploration data have been used to identify specific sites where this investment has led to a significant contribution in global mineral supply of cobalt or where a significant increase in cobalt production capacity is anticipated in the next 5 years. This report provides an overview of the cobalt industry, factors affecting mineral supply, and circumstances surrounding the development, or lack thereof, of key mineral properties with the potential to affect mineral supply. Of the 48 sites with an effective production capacity of at least 1,000 metric tons per year of cobalt considered for this study, 3 producing sites underwent significant expansion during the study period, 10 exploration sites commenced production from 1995 through 2008, and 16 sites were expected to begin production by 2013 if planned development schedules are met. Cobalt supply is influenced by economic, environmental, political, and technological factors affecting exploration for and production of copper, nickel, and other metals as well as factors affecting the cobalt industry. Cobalt-rich nickel laterite deposits were discovered and developed in Australia and the South Pacific and improvements in laterite processing technology took place during the 1990s and early in the first decade of the 21st century when mining of copper-cobalt deposits in Congo (Kinshasa) was restricted because of regional conflict and lack of investment in that country's mining sector. There was also increased exploration for and greater importance placed on cobalt as a byproduct of nickel mining in Australia and Canada. The emergence of China as a major refined cobalt producer and consumer since 2007 has changed the pattern of demand for cobalt, particularly from Africa and

Crystal Structure of the Sodium Cobaltate Deuterate Superconductor NaxCoO2o4xD2O (x=1/3)

OpenAIRE

Jorgensen, J. D.; Avdeev, M.; Hinks, D. G.; Burley, J. C.; Short, S.

2003-01-01

Neutron and x-ray powder diffraction have been used to investigate the crystal structures of a sample of the newly-discovered superconducting sodium cobaltate deuterate compound with composition Na0.31(3)CoO2o1.25(2)D2O and its anhydrous parent compound Na0.61(1)CoO2. The deuterate superconducting compound is formed by coordinating four D2O molecules (two above and two below) to each Na ion in a way that gives Na-O distances nearly equal to those in the parent compound. One deuteron of the D2...

Crystal structures of salicylideneguanylhydrazinium chloride and its copper(II) and cobalt(III) chloride complexes

International Nuclear Information System (INIS)

Chumakov, Yu. M.; Tsapkov, V. I.; Bocelli, G.; Antosyak, B. Ya.; Shova, S. G.; Gulea, A. P.

2006-01-01

The crystal structures of salicylideneguanylhydrazinium chloride hydrate hemiethanol solvate (I), salicylideneguanylhydrazinium trichloroaquacuprate(II) (II), and bis(salicylideneguanylhydrazino)cobalt(III) chloride trihydrate (III) are determined using X-ray diffraction. The structures of compounds I, II, and III are solved by direct methods and refined using the least-squares procedure in the anisotropic approximation for the non-hydrogen atoms to the final factors R = 0.0597, 0.0212, and 0.0283, respectively. In the structure of compound I, the monoprotonated molecules and chlorine ions linked by hydrogen bonds form layers aligned parallel to the (010) plane. In the structure of compound II, the salicylaldehyde guanylhydrazone cations and polymer chains consisting of trichloroaquacuprate(II) anions are joined by an extended three-dimensional network of hydrogen bonds. In the structure of compound III, the [Co(LH) 2 ] + cations, chloride ions, and molecules of crystallization water are linked together by a similar network

Making a robust carbon-cobalt(III) bond

DEFF Research Database (Denmark)

Larsen, Erik; Madsen, Anders Østergaard; Kofod, Pauli

2009-01-01

The coordination ion with a well-characterized carbon-cobalt(III) bond, the (1,4,7-triazacyclononane)(1,6-diamino-3-thia-4-hexanido)cobalt(III) dication, [Co(tacn)(C-aeaps)](2+) (aeaps, for aminoethylaminopropylsulfide), has been reacted with iodomethane, and the S-methyl thionium derivative has...... been isolated. The crystal structure of the resulting [Co(tacn)(C-aeaps-SCH(3))]Br(3) x 3 H(2)O at 122 K has been determined by X-ray diffraction techniques to verify the structure. The crystal structure determination shows that the carbon-cobalt bond length is even shorter (2.001(4) A) than in [Co......(tacn)(C-aeaps)](2+) participates in bonding to cobalt(III), having implications for the transformation between the carbon- and sulfur-bound forms of the aeaps ligand....

Total body irradiation with a reconditioned cobalt teletherapy unit.

Science.gov (United States)

Evans, Michael D C; Larouche, Renée-Xavière; Olivares, Marina; Léger, Pierre; Larkin, Joe; Freeman, Carolyn R; Podgorsak, Ervin B

2006-01-01

While the current trend in radiotherapy is to replace cobalt teletherapy units with more versatile and technologically advanced linear accelerators, there remain some useful applications for older cobalt units. The expansion of our radiotherapy department involved the decommissioning of an isocentric cobalt teletherapy unit and the replacement of a column-mounted 4-MV LINAC that has been used for total body irradiation (TBI). To continue offering TBI treatments, we converted the decommissioned cobalt unit into a dedicated fixed-field total body irradiator and installed it in an existing medium-energy LINAC bunker. This article describes the logistical and dosimetric aspects of bringing a reconditioned cobalt teletherapy unit into clinical service as a total body irradiator.

Potential for cobalt recovery from lateritic ores in Europe

Science.gov (United States)

Herrington, R.

2012-04-01

Cobalt is one of the 'critical metals' identified under the EU Raw Materials Initiative. Annually the global mine production of cobalt is around 55,000 tonnes,with Europe's industries consuming around 30% of that figure. Currently Europe produces around 27 tonnes of cobalt from mines in Finland although new capacity is planned. Co-bearing nickel laterite ores being mined in Greece, Macedonia and Kosovo where the cobalt is currently not being recovered (ores have typical analyses of 0.055% Co and >1% Ni,). These ores are currently treated directly in pyrometallurgical plants to recover the contained nickel and this process means there is no separate cobalt product produced. Hydrometallurgical treatment of mineralogically suitable laterite ores can recover the cobalt; for example Cuba recovers 3,500 tonnes of cobalt from its laterite mining operations, which are of a similar scale to the current European operations. Implementation of hydrometallurgical techniques is in its infancy in Europe with one deposit in Turkey planning to use atmospheric heap leaching to recover nickel and copper from oxide-dominated ores. More widespread implementation of these methods to mineralogically suitable ore types could unlock the highly significant undeveloped resources (with metal contents >0.04% Co and >1% Ni), which have been defined throughout the Balkans eastwards into Turkey. At a conservative estimate, this region has the potential to supply up to 30% of the EU cobalt requirements.

Temperature dependent viscosity of cobalt ferrite / ethylene glycol ferrofluids

Science.gov (United States)

Kharat, Prashant B.; Somvanshi, Sandeep B.; Kounsalye, Jitendra S.; Deshmukh, Suraj S.; Khirade, Pankaj P.; Jadhav, K. M.

2018-04-01

In the present work, cobalt ferrite / ethylene glycol ferrofluid is prepared in 0 to 1 (in the step of 0.2) volume fraction of cobalt ferrite nanoparticles synthesized by co-precipitation method. The XRD results confirmed the formation of single phase spinel structure. The Raman spectra have been deconvoluted into individual Lorentzian peaks. Cobalt ferrite has cubic spinel structure with Fd3m space group. FT-IR spectra consist of two major absorption bands, first at about 586 cm-1 (υ1) and second at about 392 cm-1 (υ2). These absorption bands confirm the formation of spinel-structured cobalt ferrite. Brookfield DV-III viscometer and programmable temperature-controlled bath was used to study the relationship between viscosity and temperature. Viscosity behavior with respect to temperature has been studied and it is revealed that the viscosity of cobalt ferrite / ethylene glycol ferrofluids increases with an increase in volume fraction of cobalt ferrite. The viscosity of the present ferrofluid was found to decrease with increase in temperature.

Use of inorganic and organic compounds as decontaminates for cobalt T-60 and cesium-134 by clover plant grown on Inshas Sandy soil

International Nuclear Information System (INIS)

Abdel-Sabour, M.F.; El-naggr, H.A.; Soliman, S.M.

1994-01-01

Out door lysimeter experiment was carried out to elucidate the effect of four inorganic and three organic salts on 60 Co and 134 Cs uptake and dry matter yield of three cuts of clover in the soil Inshas A new concept was proposed for assessing the difference in capacity of soil to supply radionuclides (i.e. 60 Co and 134 Cs) to plants as affected by applied inorganic or organic compounds. The relation of plant tissues (P c ) Co/IR Cs content with increasing time can be expressed as log (Pc) = A + B log time (T), where A and B the regression. When the same plant species is grown on the same soil differ only in the applied compound (e.g. Fe-EDDHA, Fe-DTPA, Fe-O A C, Fe(Coo)z, A1(OH)3, Ca(H2 P O 4 )2 and Fe 2 O 3 ) the equation will change to, log (P'c) = A + B' log (T) (I). Based on both equations, the relationship between (Pc) becomes; log (P'c) = [(A'B')/(A B + A B ) [ +[1/A'B + A B ) [ log (Pc) (II). The intercept (C) and slope (S) in Eq. (II) were determined among 7 treatments (for either 60 Co or 134 Cs). Then the difference of either Co or Cs accumulation with time between control and any other treatment was evaluated according to (C) and (S) values. The data also that Fe-DTPA is preferred for 60 Co as enhancing compound for plant uptake (for decontamination use); compared with other applied salts; on the other hand, any tested salts did not significantly effect 134 Cs taken by clover. Also, it was found that more than 70% of total cobalt uptake was accumulated in the roots which indicate that Co is less mobile in plants than Cs. 3 figs., 4 tabs

Synthesis of cobalt boride nanoparticles using radio frequency thermal plasma

International Nuclear Information System (INIS)

Lapitan, Jr. Lorico DS.; Ying Ying Chen; Seesoek Choe; Watanabe, Takayuki

2012-01-01

Nano size cobalt boride particles were synthesized from vapor phase using a 30 kw-4 MHz radio frequency (RF) thermal plasma. Cobalt and boron powder mixtures used as precursors in different composition and feed rate were evaporated immediately in the high temperature plasma and cobalt boride nanoparticles were produced through the quenching process. The x-ray diffractometry (XRD) patterns of cobalt boride nanoparticles prepared from the feed powder ratio of 1:2 and 1:3 for Co: B showed peaks that are associated with the Co 2 B and CoB crystal phases of cobalt boride. The XRD analysis revealed that increasing the powder feed rate results in a higher mass fraction and a larger crystalline diameter of cobalt boride nanoparticles. The images obtained by field emission scanning electron microscopy (FE-SEM) revealed that cobalt boride nanoparticles have a spherical morphology. The crystallite size of the particles estimated with XRD was found to be 18-22 nm. (author)

Study to use graded cobalt adjuster in 540 MWe PHWR

International Nuclear Information System (INIS)

Raj, Manish; Fernando, M.P.S.; Pradhan, A.S.; Kumar, A.N.

2007-01-01

Full text: There are 17 adjusters in 540 MWe PHWR, which are essentially provided for xenon override function. They also provide flux flattening being in the central region of the reactor core. The present design of adjusters consists of stainless steel tube. The adjuster rods are grouped into 8 banks for movement. Since adjusters are normally fully inserted during reactor operation, they are best suited for production of cobalt 60. The nickel-plated cobalt in the form of either slugs or pellet are used for the design of cobalt pencils. The number of pencils can be varied to optimize the reactivity load and cobalt 60 production requirement. The worth and activity of cobalt adjusters have been worked out considering different pin configuration for the adjuster assembly. To start with we have assumed all adjusters throughout its length are of the same configuration. The flux depression factors within the cobalt pencils have been considered in the estimations of the specific and total cobalt 60 activities. The option of using graded cobalt adjusters, where different pin configuration along the length is considered for better flux flattening

Investigations on bioaccumulation of cobalt by fish eggs

International Nuclear Information System (INIS)

Harms, U.; Behringer, H.; Kunze, J.

1978-01-01

In ionized form cobalt is taken up by fish eggs directly from the water. Accumulation takes place on the chorion where the metal ions are reversibly bound to functional groups of the protein of the envelope of the egg or of the mycosa. To a small extent there occurs a transport of metal ions into the interior of the egg. It could not be clarified within the scope of the studies performed if this process is to be attributed to diffusion. Binding of the cobalt ions to the chorion leads, within hours, to a nearly uncharged final state, an apparent equilibrium, whose position is determined by the cobalt ion concentration of the breeding medium. Foreign ions (electrolytes like Ca 2+ ) lead to reduced uptake of cobalt ions, because they compete with the latter for binding places in the egg's envelope. Complex-forming substances (cysteine) result in lower absorption rates, too, the concentration of available cobalt ions in the water being reduced. (orig.) [de

Measurement for cobalt target activity and its axial distribution

International Nuclear Information System (INIS)

Li Xingyuan; Chen Zigen.

1985-01-01

Cobalt target activity and its axial distribution are measured in process of producing radioactive isotopes 60 Co by irradiation in HFETR. Cobalt target activity is obtained with measured data at 3.60 m and 4.60 m, relative axial distribution of cobalt target activity is obtained with one at 30 cm, and axial distribution of cobalt target activity(or specific activity) is obtained with both of data. The difference between this specific activity and measured result for 60 Co teletherapy sources in the end is less than +- 5%

21 CFR 73.3110a - Chromium-cobalt-aluminum oxide.

Science.gov (United States)

2010-04-01

... 21 Food and Drugs 1 2010-04-01 2010-04-01 false Chromium-cobalt-aluminum oxide. 73.3110a Section... LISTING OF COLOR ADDITIVES EXEMPT FROM CERTIFICATION Medical Devices § 73.3110a Chromium-cobalt-aluminum oxide. (a) Identity. The color additive chromium-cobalt-aluminum oxide (Pigment Blue 36) (CAS Reg. No...

Characterization and Catalytic Activity of Montmorillonite K10-Supported Cobalt Catalysts

International Nuclear Information System (INIS)

Gobara, H.M.; Ghattas, M.S.; Henien, S.A.

2010-01-01

Montmorillonite K10-supported cobalt catalysts were prepared by wet impregnation method. The samples were analyzed by XRD, TPR, FTTR and BET characterization techniques. [Three phases of cobalt species were identified namely, cobalt oxide (Co 3 O 4 ), cobalt silicate (Co 2 S 1 O 4 ) and cobalt aluminate (CoAl 2 O 4 ). These species were most probably existing within the inter lamellar spaces of the meso porous montmorillonite K10 support]. The two bands observed at 1385 and 760 cm 1 were characteristic of metal species rather than the support, being mostly of Co - O bond vibration. The hysteresis loop, pore size distribution, pore volume and BET surface area were greatly affected by cobalt loading. The catalyst containing 18 wt% cobalt was the most selective sample for ethylene production from ethanol dehydration.

Radiation induced ligand loss from cobalt complexes

International Nuclear Information System (INIS)

Funston, A. M.; McFadyen, W.D.; Tregloan, P.A.

2000-01-01

Full text: Due to the rapid nature of ligand dissociation from cobalt(II) complexes the study of the rate of ligand dissociation necessitates the use of a technique such as pulse radiolysis. This allows the rapid reduction of the corresponding cobalt(III) complex by a reducing radical, such as the aquated electron, to form the cobalt(II) complex. However, to date, no systematic study of either the mechanism of reduction or the influence of the electronic structure on the rate of ligand dissociation has been carried out. In order to understand these processes more fully the mechanism of reduction of a range of related cobalt(III) complexes by the aquated electron and the subsequent rate of ligand dissociation from the resulting cobalt(II) complexes is being investigated. It has been found that a number of processes are observed following the initial rapid reaction of the cobalt(III) complex with the aquated electron. Ultimately ligand loss is observed. Depending upon the complex, the initial processes observed may include the formation of coordinated radicals and electron transfer within the complex. For complexes containing aromatic ligands such as 2,2'-bipyridine, 1,10-phenanthroline and dipyrido[3,2-a:2',3'-c]phenazine the formation of a coordinated radical is observed as the initial reduction step. The kinetics of ligand dissociation of these complexes has been determined. The loss of monodentate ligands is fast and has been indistinguishable from the reduction processes when aromatic ligands are also present in the complex. However, for diamine chelates and diimine chelates spectra of the transient species can be resolved

The cobalt-60 container scanner

International Nuclear Information System (INIS)

Jigang, A.; Liye, Z.; Yisi, L.; Haifeng, W.; Zhifang, W.; Liqiang, W.; Yuanshi, Z.; Xincheng, X.; Furong, L.; Baozeng, G.; Chunfa, S.

1997-01-01

The Institute of Nuclear Energy Technology (INET) has successfully designed and constructed a container (cargo) scanner, which uses cobalt-60 of 100-300 Ci as radiation source. The following performances of the Cobalt-60 container scanner have been achieved at INET: a) IQI (Image Quality Indicator) - 2.5% behind 100 mm of steel; b) CI (Contrast Indicator) - 0.7% behind 100 mm of steel; c) SP (Steel Penetration) - 240 mm of steel; d) Maximum Dose per Scanning - 0.02mGy; e) Throughput - twenty 40-foot containers per hour. These performances are equal or similar to those of the accelerator scanners. Besides these nice enough inspection properties, the Cobalt-60 scanner possesses many other special features which are better than accelerator scanners: a) cheap price - it will be only or two tenths of the accelerator scanner's; b) low radiation intensity - the radiation protection problem is much easier to solve and a lot of money can be saved on the radiation shielding building; c) much smaller area for installation and operation; d) simple operation and convenient maintenance; e) high reliability and stability. The Cobalt-60 container (or cargo) scanner is satisfied for boundary customs, seaports, airports and railway stations etc. Because of the nice special features said above, it is more suitable to be applied widely. Its high properties and low price will make it have much better application prospects

Highly selective cobalt-catalyzed hydrovinylation of styrene

NARCIS (Netherlands)

Grutters, M.M.P.; Müller, C.; Vogt, D.

2006-01-01

The hydrovinylation reaction is a codimerization of a 1,3-diene or vinyl arene and ethene with great potential for fine chemicals and pharmaceuticals. For the first time, enantioselective cobalt-catalyzed hydrovinylations of styrene were achieved with a cobalt-based system bearing a chiral

Mesoporous ethanesilica materials with bimodal and trimodal pore-size distributions synthesised in the presence of cobalt ions

Directory of Open Access Journals (Sweden)

Alufelwi M. Tshavhungwe

2010-07-01

Full Text Available Mesoporous organosilica materials containing ethane groups in their framework were formed with two and three pore sizes (i.e. bimodal and trimodal pores when synthesised by the sol-gel method in the presence of cobalt ions. The compounds 1,2-bistrimethoxysilylethane and tetraethylorthosilicate were used as silicon sources and the reactions were done in the presence of a surfactant, which served as a template. Diffuse reflectance infrared Fourier transform spectroscopy revealed that organic functional groups were incorporated into the ethanesilica. Powder X-ray diffraction and nitrogen adsorption data indicated that the mesophase and textural properties (surface area, pore volume, pore diameter of the materials were dependent on the ageing temperature, the amount/ratio of silica precursors and cobalt ion incorporation. Secondary mesopores were drastically reduced by changing the ratio of silicon precursors.

Cobalt Blues The Story of Leonard Grimmett, the Man Behind the First Cobalt-60 Unit in the United States

CERN Document Server

Almond, Peter R

2013-01-01

For the latter half of the 20th century, cobalt-60 units were the mainstay of radiation treatments for cancer. Cobalt Blues describes the development of the first cobalt-60 unit in the United States and the man behind it, Leonard Grimmett. Conceptually conceived before World War II, it only became possible because of the development of nuclear reactors during the war. Although Grimmett conceived of and published his ideas first, the Canadians built the first units because of the capability of their reactor to produce more suitable cobalt-60 sources. This book tells the story of how Grimmett and others came together at the time that the U S Atomic Energy Agency was pushing the use of radioactivity in medicine. Due to his sudden death, very little information about Grimmett was known until recently, when various documents have come to light, allowing the full story to be told.

S-omega carboxamidinoalkyl isothiurea compounds. VI. Radioprotective testing on E. coli

Energy Technology Data Exchange (ETDEWEB)

Minkova, M; Pantev, T [Nauchno-Izsledovatelski Inst. po Radiologiya i Radiatsionna Khigiena, Sofia (Bulgaria)

1975-01-01

The radioprotective effect of eight newly synthesized potential radioprotectors from the group of the S-omega carboxamidinoalkyl isothiourea compounds is studied. The protective activity of these compounds is evaluated according to the ability of E. coli B to form colonies. Exponential culture of this strain were exposed to 20, 40, 60, 80, 100, and 120 kR of gamma rays (Cobalt 60) in the presence of the tested compounds administered in experimentally established nontoxic concentrations 15 minutes before irradiation. Five of the eight compounds tested showed radioprotective effect which was more prominent at the higher doses. As a result of this, cell survival was increased by one order.

Sputtering on cobalt with noble gas ions

International Nuclear Information System (INIS)

Sarholt-Kristensen, L.; Johansen, A.; Johnson, E.

1983-01-01

Single crystals of cobalt have been bombarded with 80 keV Ar + ions and with 80 keV and 200 keV Xe + ions in the [0001] direction of the hcp phase and the [111] direction of the fcc phase. The sputtering yield has been measured as function of target temperature (20 0 C-500 0 C), showing a reduction in sputtering yield for 80 keV Ar + ions and 200 keV Xe + ions, when the crystal structure changes from hcp to fcc. In contrast to this, bombardment with 80 keV Xe + ions results in an increase in sputtering yield as the phase transition is passed. Sputtering yields for [111] nickel are in agreement with the sputtering yields for fcc cobalt indicating normal behaviour of the fcc cobalt phase. The higher sputtering yield of [0001] cobalt for certain combinations of ion mass and energy may then be ascribed to disorder induced partly by martensitic phase transformation, partly by radiation damage. (orig.)

Kinetic control of intralayer cobalt coordination in layered hydroxides: Co(1-0.5x)(oct) Co(x)(tet) (OH)2 (Cl)x (H2O)n.

Science.gov (United States)

Neilson, James R; Schwenzer, Birgit; Seshadri, Ram; Morse, Daniel E

2009-12-07

We report the synthesis and characterization of new structural variants of the isotypic compound with the generic chemical formula, Co(1-0.5x)(oct) Co(x)(tet) (OH)2 (Cl)x (H2O)n, all modifications of an alpha-Co(OH)2 lattice. We show that the occupancy of tetrahedrally coordinated cobalt sites and associated chloride ligands, x, is modulated by the rate of formation of the respective layered hydroxide salts from kinetically controlled aqueous hydrolysis at an air-water interface. This new level of structural control is uniquely enabled by the slow diffusion of a hydrolytic catalyst, a simple technique. Independent structural characterizations of the compounds separately describe various attributes of the materials on different length scales, revealing details hidden by the disordered average structures. The precise control over the population of distinct octahedrally and tetrahedrally coordinated cobalt ions in the lattice provides a gentle, generic method for modulating the coordination geometry of cobalt in the material without disturbing the lattice or using additional reagents. A mechanism is proposed to reconcile the observation of the kinetic control of the structure with competing interactions during the initial stages of hydrolysis and condensation.

Thorium-d-metals compounds and solid solutions

International Nuclear Information System (INIS)

Chachkhiani, Z.B.; Chechernikov, V.I.; Chachkhiani, L.G.

1986-01-01

Thorium compounds with Fe, Co, Ni dependence of their magnetic properties on temperature, pressure and concentration of the second element are considered. Anomalous magnetic behaviour of alloys in the Th-Fe system is noted. Special attention is paid to compounds with CaCu 5 type hexagonal structure and their solid solutions. Th-Co-Ni specimens containing up to 25% Ni are ferromagnetics and the rest are paramagnetics. Specimens with 60% cobalt content do not display ferromagnetic properties up to 4.2 K. Hydrides of Th 7 M 3 H 30 type (M - Fe, Co, Ni) are also considered. Highly hydrogenized specimens (under high pressure) appear to be stronger ferromagnetics

Nickel, copper and cobalt coalescence in copper cliff converter slag

Directory of Open Access Journals (Sweden)

Wolf A.

2016-01-01

Full Text Available The aim of this investigation is to assess the effect of various additives on coalescence of nickel, copper and cobalt from slags generated during nickel extraction. The analyzed fluxes were silica and lime while examined reductants were pig iron, ferrosilicon and copper-silicon compound. Slag was settled at the different holding temperatures for various times in conditions that simulated the industrial environment. The newly formed matte and slag were characterized by their chemical composition and morphology. Silica flux generated higher partition coefficients for nickel and copper than the addition of lime. Additives used as reducing agents had higher valuable metal recovery rates and corresponding partition coefficients than fluxes. Microstructural studies showed that slag formed after adding reductants consisted of primarily fayalite, with some minute traces of magnetite as the secondary phase. Addition of 5 wt% of pig iron, ferrosilicon and copper-silicon alloys favored the formation of a metallized matte which increased Cu, Ni and Co recoveries. Addition of copper-silicon alloys with low silicon content was efficient in copper recovery but coalescence of the other metals was low. Slag treated with the ferrosilicon facilitated the highest cobalt recovery while copper-silicon alloys with silicon content above 10 wt% resulted in high coalescence of nickel and copper, 87 % and 72 % respectively.

A laboratory and field evaluation of the mobility of cobalt-60/EDTA

International Nuclear Information System (INIS)

Jones, T.L.; Gee, G.W.; Kirkham, R.R.; Swanson, J.L.

1983-01-01

We have observed a time and soil type dependence in the ability of the organic complexant EDTA to keep cobalt-60 in solution. Test results indicate that short-term adsorption tests lasting 5 days or less can be misleading. In short-term tests using cobalt-60/EDTA and soil from the Hanford site, low sorption in batch tests and high mobility in column tests were observed. During long-term batch test using cobalt-60/EDTA, the percentage of cobalt remaining in solution decreased from 90% after 7 days to less than 10% after 500 days. In laboratory and field column tests where low water flow rates allowed long contact time, virtually no cobalt movement was observed even though in the field test tritium was transported over 4 meters. Long-term batch tests using cobalt-60/EDTA and soil from Savannah River burial grounds showed that cobalt remainin in solution dropped to 30% of the total cobalt added after 5 days and to less than 1% after 15 days. Batch tests using soil from Oak Ridge burial grounds were less dramatic showing cobalt in solution decreasing from 90% after 5 days to 70% after 35 days. The cobalt-60/EDTA complex appears to be dissociating and leaving uncomplexed cobalt which is readily sorbed. The dissociation seems to be rather complete in Hanford and Savannah River soil but limited in the Oak Ridge soil. The implication to waste management is that the potential for transport of cobalt by EDTA may not be as serious at all burial sites as once thought

Cobalt-related features of spectral and magnetic properties of RNi{sub 4}Co (R=Ho, Er)

Energy Technology Data Exchange (ETDEWEB)

Lukoyanov, A.V., E-mail: lukoyanov@imp.uran.ru [Institute of Metal Physics, Russian Academy of Sciences–Ural Branch, 620990 Yekaterinburg (Russian Federation); Ural Federal University, 620002 Yekaterinburg (Russian Federation); Knyazev, Yu.V.; Kuz‘min, Yu.I.; Kuchin, A.G. [Institute of Metal Physics, Russian Academy of Sciences–Ural Branch, 620990 Yekaterinburg (Russian Federation)

2014-11-15

In this paper we investigate spectral and magnetic properties of RNi{sub 4}Co (R=Ho, Er) intermetallics to reveal the features associated with the presence of Co substituting ion in comparison with the parent HoNi{sub 5} and ErNi{sub 5} compounds. Our ab initio LSDA+U calculations show that in the electronic structure Co states are strongly manifested near the Fermi energy for the case of Co in 2c position, while Co in 3g position results only in weak changes of the total DOS curve. Theoretical optical conductivity calculated assuming Co equally redistributed among 2c or 3g positions agrees well with the experimental optical conductivity. Cobalt ion in RNi{sub 4}Co (R=Ho, Er) is characterized by magnetic moment of 1μ{sub B} that increases exchange interaction in the 3d sublattice by several times that contributes to the growth of Curie temperature in comparison with the parent compounds. - Highlights: • Electronic structure of RNi4Co (R=Ho, Er) is calculated in LSDA+U. • Cobalt ion is considered in 2c or 3g position and compared. • Experimental optical conductivity is interpreted based on the calculated one.

EXAFS Determination of the Structure of Cobalt in Carbon-Supported Cobalt and Cobalt-Molybdenum Sulfide Hydrodesulfurization Catalysts.

NARCIS (Netherlands)

Koningsberger, D.C.; Bouwens, S.M.A.M.; Veen, J.A.R. van; Beer, V.H.J. de; Prins, R.

1991-01-01

The structure of the cobalt present in carbon-supported Co and Co-Mo sulfide catalysts was studied by means of X-ray absorption spectroscopy at the Co K-edge and by X-ray photoelectron spectroscopy (XPS). Thiophene hydrodesulfurization activities were used to measure the catalytic properties of

A spot test for detection of cobalt release - early experience and findings

DEFF Research Database (Denmark)

Thyssen, Jacob P; Menné, Torkil; Johansen, Jeanne D

2010-01-01

It is often difficult to establish clinical relevance of metal exposure in cobalt-allergic patients. Dermatologists and patients may incorrectly assume that many metallic items release cobalt at levels that may cause cobalt dermatitis. Cobalt-allergic patients may be unaware that they are exposed...

Incentives and opportunities for reducing the cobalt content in reactor core components

International Nuclear Information System (INIS)

Ocken, H.

1985-01-01

Cobalt in core components contributes to radiation field buildup on out-of-core surfaces. Core components containing cobalt-base alloys and cobalt as an impurity are identified. The use of cobalt-free wear-resistant alloys and construction materials with lower impurity levels of cobalt is disused. It is argued that such measures are cost effective. Lower radiation fields and disposal costs will offset higher raw material costs. Component performance will not be affected. (author)

Removal of Cobalt Ion by Adsorbing Colloidal Flotation

Energy Technology Data Exchange (ETDEWEB)

Jung, In Ha; Lee, Jung Won [Korea Atomic Energy Research Institute, Taejon (Korea)

1998-09-30

Simulated waste liquid containing 50 ppm cobalt ion was treated by adsorbing colloidal flotation using Fe(III) or Al(III) as flocculant and a sodium lauryl sulfate as a collector. Parameters such as pH, surfactant concentration, Fe(III) or Al(III) concentration, gas flow rate, etc., were considered. The flotation with Fe(III) showed 99.8% removal efficiency of cobalt on the conditions of initial cobalt ion concentration 50 ppm, pH 9.5, gas flow rate 70 ml/min, and flotation time 30 min. When the waste solution was treated with 35% H{sub 2}O{sub 2} prior to adsorbing colloidal flotation, the optimal pH for removing cobalt shifted to weak alkaline range and flotation could be applied in wider range of pH as compared to non-use of H{sub 2}O{sub 2}. Additional use of 20 ppm Al(III) after precipitation of 50 ppm Co(II) with 50 ppm Fe(III) made the optimal pH range for preferable flotation wider. Foreign ions such as, NO{sub 3}{sup -}, SO{sub 4}{sup 2-}, Na{sup +}, Ca{sup 2+} were adopted and their effects were observed, Of which sulfate ion was found to be detrimental to removal of cobalt ion by flotation. Coprecipitation of Co ion with Fe(III) and Al(III) resulted in better removal efficiency of cobalt ion in the presence of sulfate ion. (author). 14 refs., 13 figs.

Heating analysis of cobalt adjusters in reactor core

International Nuclear Information System (INIS)

Mei Qiliang; Li Kang; Fu Yaru

2011-01-01

In order to produce 60 Co source for industry and medicine applications in CANDU-6 reactor, the stainless steel adjusters were replaced with the cobalt adjusters. The cobalt rod will generate the heat when it is irradiated by neutron and γ ray. In addition, 59 Co will be activated and become 60 Co, the ray released due to 60 Co decay will be absorbed by adjusters, and then the adjusters will also generate the heat. So the heating rate of adjusters to be changed during normal operation must be studied, which will be provided as the input data for analyzing the temperature field of cobalt adjusters and the relative heat load of moderator. MCNP code was used to simulate whole core geometric configuration in detail, including reactor fuel, control rod, adjuster, coolant and moderator, and to analyze the heating rate of the stainless steel adjusters and the cobalt adjusters. The maximum heating rate of different cobalt adjuster based on above results will be provided for the steady thermal hydraulic and accident analysis, and make sure that the reactor is safe on the thermal hydraulic. (authors)

The effect of gaseous ammonia on cobalt perrhenate

International Nuclear Information System (INIS)

Maslov, L.P.; Men'shikov, O.D.; Borisov, V.V.; Sorokin, S.I.; Krutovertsev, S.A.; Kharkevich, S.I.; Ivanova, O.M.

1994-01-01

The influence of humid air ammonia mixture on crystal pentahydrate of cobalt(2) perrhenate has been studied by the methods of PES, IR spectroscopy thermal analysis and electrophysical measurements. It is shown that with an increase in ammonia content in gaseous phase cobalt perrhenate successively transforms into diaquodiammine-, tetrammine- and μ-dioxo-bis-(tetrammine) derivatives of cobalt. Reversibility of dioxocomplex formation and a correlation between the change in electrophysical properties of crystal sample and change in ammonia content in gaseous phase are pointed out. 16 refs.; 4 figs.; 1 tab

Enhanced sintering and conductivity study of cobalt or nickel doped solid solution of barium cerate and zirconate

DEFF Research Database (Denmark)

Ricote, Sandrine; Bonanos, Nikolaos

2010-01-01

BaZr(0.9 − x)CexY(0.1 − y)CoyO(3 − δ) (with x = 0 and 0.2; y = 0.01; 0.02; 0.05) and BaZr(0.9 − x)CexY(0.1 − y)NiyO(3 − δ) (with x = 0 and 0.2; y = 0.01; 0.02) compounds have been synthesized by solid state reaction at 1400 °C and obtained as dense pellets after sintering at 1450 °C. Cobalt...... or nickel doping reduces the sintering temperature by about 250 °C. The samples are stable in a CO2 rich atmosphere at 600 °C but the 5% B site Co doped samples are aging in wet atmosphere. The conductivity has been measured for the 1 and 2% doped samples (both cobalt and nickel), in different wet...

Nitrogen induced ferromagnetism in Cobalt doped BaTiO3

Directory of Open Access Journals (Sweden)

Chandrima Mitra

2012-09-01

Full Text Available The electronic structure and magnetism of Cobalt doped BaTiO3 (BaTi1−xCoxO3 is investigated. Substitutional Nitrogen on an Oxygen site is found to play an important role in inducing net magnetic moments in the system. The presence of a Nitrogen atom as nearest neighbour to a Cobalt atom is crucial in producing spin splitting of both the Nitrogen and Cobalt states thereby introducing a net local magnetic moment. The introduction of Nitrogen is further found to enhance ferromagnetic interactions between Cobalt atoms.

Analysis of radioactive cobalt

International Nuclear Information System (INIS)

1977-01-01

This is a manual published by Science and Technology Agency, Japan, which prescribes on the analysis method for radioactive cobalt which is a typical indexing nuclide among the radioactive nuclides released from nuclear facilities. Since the released cobalt is mainly discharged to coastal region together with waste water, this manual is written for samples of sea water, sea bottom sediments and marine organisms. Radioactive cobalt includes the nuclides of 57 co, 58 Co, 60 Co, etc., the manual deals with them as a whole as 60 Co of long half life. Though 60 Co analysis has become feasible comparatively simply due to scintillation or semi-conductor spectrometry, trace 60 Co analysis is performed quantitatively by co-precipitation or collection into alumina and scintillation spectrometry. However, specific collecting operation and γ-γ coincidence measurement have been required so far. This manual employs 60 Co collection by means of ion-exchange method and measurement with low background GM counting system, to analyze quantitatively and rapidly low level 60 Co. It is primarily established as the standard analyzing method for the survey by local autonomous bodies. It is divided into 4 chapters including introduction sea water, marine organisms, and sea bottom sediments. List of required reagents is added in appendix. (Wakatsuki, Y.)

Nano cobalt oxides for photocatalytic hydrogen production

KAUST Repository

Mangrulkar, Priti A.

2012-07-01

Nano structured metal oxides including TiO 2, Co 3O 4 and Fe 3O 4 have been synthesized and evaluated for their photocatalytic activity for hydrogen generation. The photocatalytic activity of nano cobalt oxide was then compared with two other nano structured metal oxides namely TiO 2 and Fe 3O 4. The synthesized nano cobalt oxide was characterized thoroughly with respect to EDX and TEM. The yield of hydrogen was observed to be 900, 2000 and 8275 mmol h -1 g -1 of photocatalyst for TiO 2, Co 3O 4 and Fe 3O 4 respectively under visible light. It was observed that the hydrogen yield in case of nano cobalt oxide was more than twice to that of TiO 2 and the hydrogen yield of nano Fe 3O 4 was nearly four times as compared to nano Co 3O 4. The influence of various operating parameters in hydrogen generation by nano cobalt oxide was then studied in detail. Copyright © 2012, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.

Synthesis and characterization of cobalt-manganese oxides

International Nuclear Information System (INIS)

Valencia, J.; Arias, N.P.; Giraldo, O.; Rosales-Rivera, A.

2012-01-01

Cobalt doped/un-doped manganese oxides materials were synthesized at various doping rates by soft chemical reactions, oxidation-reduction method, which allows generating a metal-mixed oxide. The synthesized materials were characterized using several techniques including chemical analysis, X-rays diffraction (XRD), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), and vibrating sample magnetometer (VSM). The chemical analysis confirmed the presence of cobalt in the samples. XRD patterns reveal mainly a spinel-like structure and SEM micrographs exhibited morphology with fine aggregate of particles. TGA profiles showed weight loss due to loss of water in a first step, followed by a loss of oxygen from the lattice associated with partial reduction of Mn 4+ to Mn 3+ . VSM was used to measure the magnetization as a function of the applied magnetic field at temperatures T=50 and 300 K. Different magnetic behaviors were observed when cobalt percentage changed in the samples. These behaviors are considered to be related to the size of the particles and composition of the materials. Higher coercive field and lesser magnetization were observed for the sample with higher cobalt content.

Genotoxicity assessment of cobalt chloride in Eisenia hortensis earthworms coelomocytes by comet assay and micronucleus test.

Science.gov (United States)

Ciğerci, İbrahim Hakkı; Ali, Muhammad Muddassir; Kaygısız, Şöhret Yüksek; Liman, Recep

2016-02-01

Cobalt and its different compounds are extensively used worldwide and considered as possible environmental pollutant. Earthworms are useful model organism and its different species are used to monitor soil pollution. No study has been found to detect cobalt chloride (CoCl2) genotoxicity in earthworms. So, current study aimed to evaluate CoCl2 induced genotoxicity in Eisenia hortensis earthworms coelomocytes by alkaline comet assay (CA) and micronucleus (MN) test. The earthworms (n = 10 for each group) were exposed to different series of CoCl2 concentrations (100 ppm, 200 ppm, 300 ppm, 400 ppm, 500 ppm, 600 ppm) to find LD50. The LD50 for CoCl2 was found at 226 ppm. Then, doses of LD50/2, LD50 and 2XLD50 for 48 h were used. CA and MN demonstrated the significant increase (P earthworms. Copyright © 2015 Elsevier Ltd. All rights reserved.

Total quality management of cobalt-60 sources

International Nuclear Information System (INIS)

Malkoske, G.R.

1999-01-01

Total Quality Management of Cobalt-60 sources by a supplier requires a life cycle approach to source management. This covers various aspects, including design, manufacturing, installation, field inspection, source surveillance and return of cobalt-60 sources at the end of their useful life. The Total Quality Management approach demonstrates a strong industry commitment to the beneficial use of gamma technology for industrial irradiation applications in both developed nations and in those nations who are developing their infrastructure and techniques for the beneficial use of this technology. MDS Nordion continues to demonstrate its support and commitment to the industry by developing and implementing state-of-the-art standards for the safe use of cobalt-60 sources

Solubility of cobalt in primary circuit solutions

International Nuclear Information System (INIS)

Lambert, I.; Joyer, F.

1992-01-01

The solubility of cobalt ferrite (CoFe 2 O 4 ) was measured in PWR primary circuit conditions, in the temperature range 250-350 deg C, and the results were compared with the ones obtained on magnetite and nickel ferrite. As in the former cases, it was found that, in the prevailing primary circuit conditions, the solubility of the cobalt ferrite was minimum at temperatures around 300 deg C, for cobalt as well as for iron. The equilibrium iron concentration is significantly lower than in the case of magnetite. The results are discussed in relation with the POTHY code, based only on thermodynamic laws and data, used for the prediction of the primary circuit chemistry

Charge-lattice interplay in layered cobaltates RBaCo2O5+x

Science.gov (United States)

Lavrov, A. N.; Kameneva, M. Yu.; Kozeeva, L. P.; Zhdanov, K. R.

2017-10-01

X-ray diffraction, electrical resistivity and thermal expansion measurements are used to study the interrelation between the structural, magnetic and electron-transport peculiarities in RBaCo2O5+x (R=Y, Gd) over a wide range of oxygen contents. We find that the anisotropic lattice strain caused by the oxygen chain ordering in these compounds favors the metallic state and is a necessary condition for the coupled insulator-to-metal and spin-state phase transitions to occur. The obtained data point to the key role of the crystal lattice in selecting the preferred spin and orbital states of cobalt ions.

Cobalt source calibration

International Nuclear Information System (INIS)

Rizvi, H.M.

1999-01-01

The data obtained from these tests determine the dose rate of the two cobalt sources in SRTC. Building 774-A houses one of these sources while the other resides in room C-067 of Building 773-A. The data from this experiment shows the following: (1) The dose rate of the No.2 cobalt source in Building 774-A measured 1.073 x 10 5 rad/h (June 17, 1999). The dose rate of the Shepherd Model 109 Gamma cobalt source in Building 773-A measured 9.27 x 10 5 rad/h (June 25, 1999). These rates come from placing the graduated cylinder containing the dosimeter solution in the center of the irradiation chamber. (2) Two calibration tests in the 774-A source placed the graduated cylinder with the dosimeter solution approximately 1.5 inches off center in the axial direction. This movement of the sample reduced the measured dose rate 0.92% from 1.083 x 10 5 rad/h to 1.073 x 10 5 rad/h. and (3) A similar test in the cobalt source in 773-A placed the graduated cylinder approximately 2.0 inches off center in the axial direction. This change in position reduced the measured dose rate by 10.34% from 1.036 x 10 6 to 9.27 x 10 5 . This testing used chemical dosimetry to measure the dose rate of a radioactive source. In this method, one determines the dose by the chemical change that takes place in the dosimeter. For this calibration experiment, the author used a Fricke (ferrous ammonium sulfate) dosimeter. This solution works well for dose rates to 10 7 rad/h. During irradiation of the Fricke dosimeter solution the Fe 2+ ions ionize to Fe 3+ . When this occurs, the solution acquires a slightly darker tint (not visible to the human eye). To determine the magnitude of the change in Fe ions, one places the solution in an UV-VIS Spectrophotometer. The UV-VIS Spectrophotometer measures the absorbency of the solution. Dividing the absorbency by the total time (in minutes) of exposure yields the dose rate

Benzimidazoles: A biologically active compounds

Directory of Open Access Journals (Sweden)

Salahuddin

2017-02-01

Full Text Available Synthesis of commercially available benzimidazole involves condensation of o-phenylenediamine with formic acid. The most prominent benzimidazole compound in nature is N-riosyldimethylbenzimidazole, which serves as a axial ligand for cobalt in vitamin B12. The benzimidazole and its derivatives play a very important role as a therapeutic agent e.g. antiulcer and anthelmintic drugs. Apart from this the benzimidazole derivatives exhibit pharmacological activities such as antimicrobial, antiviral, anticancer, anti-inflammatory, analgesic, etc. The substituted benzimidazoles are summarized in this review to know about the chemistry as well as pharmacological activities.

Piezoelectric properties and thermal stabilities of cobalt-modified potassium bismuth titanate

International Nuclear Information System (INIS)

Guo, Zhen-Lei; Wang, Chun-Ming; Zhao, Tian-Long; Yu, Si-Long; Cao, Zhao-Peng

2013-01-01

The cobalt-modified potassium bismuth titanate (K 0.5 Bi 4.5 Ti 4 O 15 , KBT) piezoelectric ceramics have been prepared using conventional solid–state reaction. X-ray diffraction analysis revealed that the cobalt-modified KBT ceramics have a pure four-layer (m = 4) Aurivillius-type structure. The dielectric, ferroelectric, and piezoelectric properties of cobalt-modified KBT ceramics were investigated in detail. The piezoelectric activities of KBT ceramics were significantly improved by the cobalt modification. The reasons for piezoelectric activities enhancement with cobalt modification were given. The piezoelectric coefficient d 33 and Curie temperature T c for the 5 mol% cobalt-modified KBT ceramics (KBT-Co5) were found to be 28 pC/N and 575 °C, respectively. The DC resistivity, frequency constants (N p and N t ), and electromechanical properties at elevated temperature were investigated, indicating the cobalt-modified KBT piezoelectric ceramics possess stable piezoelectric properties up to 500 °C. The results show the cobalt-modified KBT ceramics are potential materials for high temperature piezoelectric applications. - Highlights: • We examine the piezoelectric properties of the cobalt-modified K 0.5 Bi 4.5 Ti 4 O 15 . • A high level of piezoelectric activities (d 33 = 28 pC/N) are obtained. • High Curie temperature (T c = 575 °C) is acquired for the optimal composition. • The Co-modified K 0.5 Bi 4.5 Ti 4 O 15 is promising as high temperature materials

The cobalt radioactive isotopes in environment; Les isotopes radioactifs du cobalt dans l'environnement

Energy Technology Data Exchange (ETDEWEB)

NONE

2007-07-01

For the year 1993 the total activity released in cobalt is 69 GBq for the whole of nuclear power plants. The part of activity in cobalt for La Hague in 1993 is 8 GBq of {sup 58}Co and 2 GBq of {sup 60}Co. The radioactive isotopes released by nuclear power plants or the reprocessing plant of La Hague under liquid effluents are shared by half between {sup 58}Co and {sup 60}Co. The exposure to sealed sources is the most important risk for the cobalt. The risk of acute exposure can associate a local irradiation of several decades of grays inducing a radiological burns, deep burn to treat in surgery by resection or graft even amputation. A global irradiation of organism for several grays induces an acute irradiation syndrome, often serious. At long term the stochastic effects are represented by leukemia and radio-induced cancers. The increase of probability of their occurrence is 1% by sievert. We must remind that the natural spontaneous probability is 25%. (N.C.)

Separation of cobalt from synthetic intermediate and decontamination radioactive wastes using polyurethane foam

International Nuclear Information System (INIS)

Rao, S.V.S.; Lal, K.B.; Narasimhan, S.V.; Ahmed, J.

1997-01-01

Studies have been carried out on the removal of radioactive cobalt ( 60 Co) from synthetic intermediate level waste (ILW) and decontamination waste using neat polyurethane (PU) foam as well as n-tributyl phosphate-polyurethane (TBP-PU) foam. The radioactive cobalt has been extracted on the PU foam as cobalt thiocyanate from the ILW. Maximum removal of cobalt has been observed when the concentration of thiocyanate in the solution is about 0.4 M. Cobalt can be separated from decontamination waste containing ethylenediaminetetraacetic acid (EDTA) and iron(II). The extent of extraction of cobalt is slow and the separation of iron and cobalt is better with the neat PU foam compared to the TBP-PU foam. The presence of iron in the decontamination waste facilitates the extraction of cobalt thiocyanate on the PU foam. Column studies have been carried out in order to extend these studies to the plant scale. The capacities of the PU foams for cobalt have been determined. The effect of density and the surface area of PU foam have been investigated. Fourier Transform Infrared (FT-IR) spectral studies have been conducted to find out the interaction between PU foam and cobalt thiocyanate species

Mitigation of cesium and cobalt contamination on the surfaces of RAM packages

International Nuclear Information System (INIS)

Krumhansl, J.; Bonhomme, F.; McConnell, P.; Kapoor, A.

2004-01-01

Techniques for mitigating the adsorption of 137 Cs and 60 Co on metal surfaces (e.g., RAM packages) exposed to contaminated water (e.g., spent-fuel pools) has been developed and experimentally verified. The techniques are also effective in removing some of the 60 Co and 137 Cs that may have been adsorbed on the surfaces after removal from the contaminated water. The principle for the 137 Cs mitigation technique is based upon ion-exchange processes. In contrast, 60 Co contamination primarily resides in minute particles of CRUD that become lodged on cask surfaces. CRUD is an insoluble Fe-Ni-Cr oxide that forms colloidal-sized particles as stainless steels corrode. Because of the similarity between Ni +2 and Co +2 , CRUD is able to scavenge and retain traces of cobalt as it forms. A number of organic compounds have a great specificity for combining with nickel and cobalt. Ongoing research is investigating the effectiveness of chemical complexing agent, EDTA, with regard to its ability to dissolve the host phase (CRUD) thereby liberating the entrained 60Co into a solution where it can be rinsed away

Characterization of a Cobalt-Tungsten Interconnect

DEFF Research Database (Denmark)

Harthøj, Anders; Holt, Tobias; Caspersen, Michael

2012-01-01

is to act both as a diffusion barrier for chromium and provide better protection against high temperature oxidation than a pure cobalt coating. This work presents a characterization of a cobalt-tungsten alloy coating electrodeposited on the ferritic steel Crofer 22 H which subsequently was oxidized in air......A ferritic steel interconnect for a solid oxide fuel cell must be coated in order to prevent chromium evaporation from the steel substrate. The Technical University of Denmark and Topsoe Fuel Cell have developed an interconnect coating based on a cobalt-tungsten alloy. The purpose of the coating...... for 300 h at 800 °C. The coating was characterized with Glow Discharge Optical Spectroscopy (GDOES), Scanning Electron Microscopy (SEM) and X-Ray Diffraction (XRD). The oxidation properties were evaluated by measuring weight change of coated samples of Crofer 22 H and Crofer 22 APU as a function...

Association between cobalt allergy and dermatitis caused by leather articles

DEFF Research Database (Denmark)

Bregnbak, David; Thyssen, Jacob P; Zachariae, Claus

2015-01-01

BACKGROUND: Cobalt is a strong skin sensitizer and a prevalent contact allergen. Recent studies have recognized exposure to leather articles as a potential cause of cobalt allergy. OBJECTIVES: To examine the association between contact allergy to cobalt and a history of dermatitis resulting from...... exposure to leather. METHODS: A questionnaire case-control study was performed: the case group consisted of 183 dermatitis patients with a positive patch test reaction to cobalt chloride and a negative patch test reaction to potassium dichromate; the control group consisted of 621 dermatitis patients who...... did not react to either cobalt or chromium in patch testing. Comparisons were made by use of a χ(2) -test, Fisher's exact, and the Mann-Whitney test. Logistic regression analyses were used to test for associations while taking confounding factors into consideration. RESULTS: Leather was observed...

Syntheses, structures and magnetic properties of two new one-dimensional cobalt (II) phosphites with organic amines acting as ligands

International Nuclear Information System (INIS)

Li Gaijuan; Xing Yan; Song Shuyan

2008-01-01

Two new one-dimensional (1D) inorganic-organic hybrid cobalt (II) phosphites Co(HPO 3 ) (py) (1) and [Co(OH)(py) 3 ][Co(py) 2 ][HPO 2 (OH)] 3 (2) have been prepared under solvothermal conditions in the presence of pyridine (py). Compound 1 crystallizes in the monoclinic system, space group p2(1)/c, a=5.3577(7) A, b=7.7503(10) A, c=17.816(2) A, β=94.327(2) o , V=737.67(16) A 3 , Z=4. Compound 2 is orthorhombic, Cmcm, a=16.3252(18) A, b=15.7005(16) A, c=13.0440(13) A, β=90.00 o V=3343.4(6) A 3 and Z=4. Compound 1 possesses a 1D ladder-like framework constructed from CoO 3 N tetrahedral, HPO 3 pseudo-pyramids and pyridine ligands. While compound 2 is an unusual inorganic-organic hybrid 1D chain, which consists of corner-shared six-membered rings made of CoO 3 N 3 /CoO 4 N 2 octahedra and HPO 3 pseudo-pyramids through sharing vertices. - Graphical abstract: Two new 1D inorganic-organic hybrid cobalt (II) phosphites have been prepared under solvothermal conditions in the presence of pyridine. Co(HPO 3 ) (py) possesses a 1D ladder-like framework constructed from CoO 3 N tetrahedral, HPO 3 pseudo-pyramids and pyridine ligands (left); 1D-chain structure of [Co(OH)(py) 3 ][Co(py) 2 ][HPO 2 (OH)] 3 consists of corner-shared six-membered rings (right)

Multiwalled Carbon Nanotubes Decorated with Cobalt Oxide Nanoparticles

Directory of Open Access Journals (Sweden)

D. G. Larrude

2012-01-01

Full Text Available Multiwalled carbon nanotubes (MWCNTs synthesized by spray pyrolysis were decorated with cobalt oxide nanoparticles using a simple synthesis route. This wet chemistry method yielded nanoparticles randomly anchored to the surface of the nanotubes by decomposition of cobalt nitrate hexahydrate diluted in acetone. Electron microscopy analysis indicated that dispersed particles were formed on the MWCNTs walls. The average size increased with the increasing concentration of cobalt nitrate in acetone in the precursor mixture. TEM images indicated that nanoparticles were strongly attached to the tube walls. The Raman spectroscopy results suggested that the MWCNT structure was slightly damaged after the nanoparticle growth.

Transport properties of cobalt at low temperatures

DEFF Research Database (Denmark)

Radharkishna, P.; Nielsen, Mourits

1965-01-01

Measurements are made of electrical resistivity, absolute thermoelectric power, and thermal conductivity of polycrystalline cobalt between 1.2 and 6 K; results are discussed on basis of inter-electronic scattering.......Measurements are made of electrical resistivity, absolute thermoelectric power, and thermal conductivity of polycrystalline cobalt between 1.2 and 6 K; results are discussed on basis of inter-electronic scattering....

Perfluorinated cobalt phthalocyanine effectively catalyzes water electrooxidation

KAUST Repository

Morlanes, Natalia Sanchez

2014-12-08

Efficient electrocatalysis of water oxidation under mild conditions at neutral pH was achieved by a fluorinated cobalt phthalocyanine immobilized on fluorine-doped tin oxide (FTO) surfaces with an onset potential at 1.7 V vs. RHE. Spectroscopic, electrochemical, and inhibition studies indicate that phthalocyanine molecular species are the operational active sites. Neither free cobalt ions nor heterogeneous cobalt oxide particles or films were observed. During long-term controlled-potential electrolysis at 2 V vs. RHE (phosphate buffer, pH 7), electrocatalytic water oxidation was sustained for at least 8 h (TON ≈ 1.0 × 105), producing about 4 μmol O2 h-1 cm-2 with a turnover frequency (TOF) of about 3.6 s-1 and no measurable catalyst degradation.

A spot test for detection of cobalt release – early experience and findings

DEFF Research Database (Denmark)

Thyssen, Jacob P.; Menné, Torkil; Johansen, Jeanne D.

2010-01-01

Background: It is often difficult to establish clinical relevance of metal exposure in cobalt-allergic patients. Dermatologists and patients may incorrectly assume that many metallic items release cobalt at levels that may cause cobalt dermatitis. Cobalt-allergic patients may be unaware that they...

Assessment of cobalt levels in wastewater, soil and vegetable ...

African Journals Online (AJOL)

User

Key words: Cobalt level, Kubanni River, soil, vegetable, wastewater. INTRODUCTION. Cobalt is ... metals released into the environment from a variety of anthropogenic activities ..... Heavy Metal Stress in Plants, 2nd Edition,. Springer,. United.

Synthesis and phosphatase activity of a Cobalt(II) phenanthroline ...

Indian Academy of Sciences (India)

MAMONI GARAI

2017-09-19

Sep 19, 2017 ... Synthesis and phosphatase activity of a Cobalt(II) phenanthroline complex. MAMONI GARAIa ... tion, cobalt complexes have gained importance because of their application as ... 2.3 Physical measurements. Infrared spectrum ...

Correlation between morphology and magnetic properties of electrochemically produced cobalt powder particles

Directory of Open Access Journals (Sweden)

Maksimović Vesna M.

2015-01-01

Full Text Available Cobalt 3D powder particles were successfully prepared by the galvanostatic electrodeposition. Electrodeposited cobalt powder were characterized by X-ray diffraction (XRD, scanning electron microscope (SEM, Energy Dispersive Spectroscopy (EDS analysis and SQUID magnetometry. It has been shown that morphology, structure and magnetic properties of cobalt particles are closely associated and can be easily controlled by adjusting process parameters of electrodeposition. Morphology of cobalt powder particles is strongly affected by hydrogen evolution reaction as a parallel reaction to cobalt electrodeposition. Depending on the applied current density, the two types of powder particles were formed: dendrites at lower and spongy-like particles at higher current densities. Morphologies and structures of powder particles are correlated with their magnetic properties, and compared with those of the bulk cobalt. In comparison with the properties of bulk cobalt, the obtained 3D structures exhibited a decreased saturation magnetization (MS, but an enhanced coercivity (HC which is explained by their peculiar morphology. [Projekat Ministarstva nauke Republike Srbije, br. III 45012

Study of Gel Growth Cobalt (II Oxalate Crystals as Precursor of Co3O4 Nano Particles

Directory of Open Access Journals (Sweden)

Yuniar Ponco Prananto

2013-03-01

Full Text Available Crystal growth of cobalt (II oxalate in silica gel at room temperature as precursor of Co3O4 nano particles has been studied. Specifically, this project is focusing on the use of two different reaction tube types toward crystallization of cobalt (II oxalate in gel. The gel was prepared at pH 5 by reacting sodium metasilicate solution with dilute nitric acid (for U-tube and oxalic acid (for straight tube, with gelling time of 4 days and crystal growth time of 8 (for straight tube and 12 (for U-tube weeks. Result shows that pink crystalline powder was directly formed using straight tube method. The use of different solvents in straight tube method affects crystallization and could delay direct precipitation of the product. In contrast, bigger and better shape of red block crystal was yielded from U-tube method; however, longer growth time was needed. FTIR studies suggest that both growth method produces identical compound of hydrated cobalt (II oxalate. © 2013 BCREC UNDIP. All rights reservedReceived: 25th October 2012; Revised: 30th November 2012; Accepted: 5th December 2012[How to Cite: Y.P. Prananto, M.M. Khunur, D.T. Wahyuni, R.A. Shobirin, Y.R. Nata, E. Riskah, (2013. Study of Gel Growth Cobalt (II Oxalate Crystals as Precursor of Co3O4 Nano Particles. Bulletin of Chemical Reaction Engineering & Catalysis, 7 (3: 198-204. (doi:10.9767/bcrec.7.3.4066.198-204][Permalink/DOI: http://dx.doi.org/10.9767/bcrec.7.3.4066.198-204 ] View in  |

Synthesis and characterization of cobalt-manganese oxides

Energy Technology Data Exchange (ETDEWEB)

Valencia, J. [Laboratorio de Magnetismo y Materiales Avanzados, Facultad de Ciencias Exactas y Naturales, Universidad Nacional de Colombia, Sede Manizales, Manizales (Colombia); Department of Aerospace Engineering and Mechanics, University of Minnesota, Minneapolis 55455-0153 (United States); Arias, N.P. [Laboratorio de Materiales Nanoestructurados y Funcionales, Facultad de Ciencias Exactas y Naturales, Universidad Nacional de Colombia, Sede Manizales, Manizales (Colombia); Departamento de Ingenieria Electrica, Electronica y Computacion, Facultad de Ingenieria y Arquitectura, Universidad Nacional de Colombia, Sede Manizales, Manizales (Colombia); Giraldo, O. [Laboratorio de Materiales Nanoestructurados y Funcionales, Facultad de Ciencias Exactas y Naturales, Universidad Nacional de Colombia, Sede Manizales, Manizales (Colombia); Rosales-Rivera, A., E-mail: arosalesr@unal.edu.co [Laboratorio de Magnetismo y Materiales Avanzados, Facultad de Ciencias Exactas y Naturales, Universidad Nacional de Colombia, Sede Manizales, Manizales (Colombia)

2012-08-15

Cobalt doped/un-doped manganese oxides materials were synthesized at various doping rates by soft chemical reactions, oxidation-reduction method, which allows generating a metal-mixed oxide. The synthesized materials were characterized using several techniques including chemical analysis, X-rays diffraction (XRD), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), and vibrating sample magnetometer (VSM). The chemical analysis confirmed the presence of cobalt in the samples. XRD patterns reveal mainly a spinel-like structure and SEM micrographs exhibited morphology with fine aggregate of particles. TGA profiles showed weight loss due to loss of water in a first step, followed by a loss of oxygen from the lattice associated with partial reduction of Mn{sup 4+} to Mn{sup 3+}. VSM was used to measure the magnetization as a function of the applied magnetic field at temperatures T=50 and 300 K. Different magnetic behaviors were observed when cobalt percentage changed in the samples. These behaviors are considered to be related to the size of the particles and composition of the materials. Higher coercive field and lesser magnetization were observed for the sample with higher cobalt content.

Estimation of cobalt release from feed water heater tubes of BWRs

International Nuclear Information System (INIS)

Uchida, S.; Kitamura, M.; Ozawa, Y.

1983-01-01

To evaluate the release source of cobalt from heater tubes of the feed water line, release rate measurements were carried out by detecting 60 Co released from irradiated stainless steel in contact with neutral water at an oxygen concentration of 20 ppb. The dependences of cobalt release rate on temperature, flow velocity and exposure time were studied after 670 hours of release experiments, and an empirical equation (which is presented) was obtained in the temperature range from 150 to 240 deg C. A decrease in the cobalt release rate above 250 deg C was considered due to the formation of a protective oxide layer. From these data, the amount of cobalt released from individual feed water heaters was evaluated. It was demonstrated that low cobalt containing stainless steel was economically applied only in the higher temperature region of the heater (20% of the total surface) to reduce cobalt feed rate into the reactor (to approx. 1/2). (author)

New perspectives in the Fischer-Tropsch synthesis using cobalt supported on mesoporous molecular sieves; Novas perspectivas na sintese de Fischer-Tropsch usando cobalto suportado em peneiras moleculares mesoporosas

Energy Technology Data Exchange (ETDEWEB)

Souza, M.J.B.; Silva, A.O.S. [Universidade Federal do Rio Grande do Norte (UFRN), Natal, RN (Brazil). Dept. de Engenharia Quimica; Fernandes Junior, V.J.; Araujo, A.S. [Universidade Federal do Rio Grande do Norte (UFRN), Natal, RN (Brazil). Dept. de Quimica

2004-07-01

The conversion of synthesis gas to liquid products via Fischer-Tropsch synthesis (FTS) is an important process in the generation of clean fuels of sulfur and nitrogen compounds. Catalysts based on iron are very used in the conventional process due its cheap manufacture price. Recently the use of cobalt as promoter gave good results. MCM-41 mesoporous materials were discovered by Mobil scientists in the nineties and ever since they have great successes as support and catalyst in several processes of the oil industry as catalytic cracking, reformer and hydrotreating. In this work are presented new alternatives for FTS with the use of cobalt supported on molecular sieves of the type MCM-41. A comparative study with the usual catalysts based on silica was accomplished with different levels of cobalt. (author)

A novel method to synthesize cobalt oxide (Co3O4) nanowires from cobalt (Co) nanobowls

DEFF Research Database (Denmark)

Srivastava, Akhilesh Kumar; Madhavi, S.; Ramanujan, R.V.

2010-01-01

A novel method suitable for the synthesis of the cobalt oxide (Co3O4) nanowires at targeted regions is presented in this report. Cobalt (Co) nanobowls synthesized by colloidal crystal directed assembly were transformed into Co3O4 nanowires by a simple heat treatment process. Co nanobowls exhibited...... a two phase (h.c.p. + f.c.c.) microstructure while single phase microstructure was observed for Co3O4 nanowires. Ferromagnetic Co nanobowls showed a dependence of coercivity on bowl size while Co3O4 exhibited weak ferromagnetic behavior....

A review of cobalt adsorption on transition metal oxides

International Nuclear Information System (INIS)

Walker, S.M.

1987-04-01

This report reviews studies of cobalt adsorption on transition metal oxides, in the context of corrosion product and radioactivity transport in PWR primary circuits. In general, uptake of cobalt increases with pH, with temperature and with decreasing ionic strength. Very little data are available under PWR primary circuit conditions, but the limited data available suggest that cobalt uptake by the zirconium oxide corrosion product layer on fuel pins may be significant compared to that deposited on fuel crud. If fuel crud levels can be reduced in future by coolant chemistry control then uptake by the zirconia will assume a greater relative role. It is planned to use an autoclave to study uptake of cobalt on oxidised Zircaloy surfaces at temperatures up to 593K under PWR primary circuit chemistry conditions. (author)

Ion exchange of Cobalt and Cadmium in Zeolite X

International Nuclear Information System (INIS)

Nava M, I.

1994-01-01

The growing development in the industry has an important contribution to the environmental damage, where the natural effluents are each day more contaminated by toxic elements, such as: mercury, chromium, lead and cadmium. So as to separate such elements it has sorbent must have enough stability, and have a sharp capacity of sorption. In this work it was studied the sorption behavior of cobalt and on the other hand, cadmium in aqueous solutions, which along with sodic form of the Zeolite X, undergoes a phenomenon of ionic interchange. Such interchange was verify to different concentration of cadmium, cobalt and hydronium ion. The content of cobalt and sodium in the interchanged samples was detected through the neutronic activation analysis. The results disclose a higher selectivity for cadmium than cobalt. (Author)

Cobalt(II Complexes with N,N,N-Scorpionates and Bidentate Ligands: Comparison of Hydrotris(3,5-dimethylpyrazol-1-ylborate Tp* vs. Phenyltris(4,4-dimethyloxazolin-2-ylborate ToM to Control the Structural Properties and Reactivities of Cobalt Centers

Directory of Open Access Journals (Sweden)

Toshiki Nishiura

2018-06-01

Full Text Available Scorpionate ligands Tp* (hydrotris(3,5-dimethylpyrazol-1-ylborate and ToM (tris(4,4-dimethyloxazolin-2-ylphenylborate complexes of cobalt(II with bidentate ligands were synthesized. Both Tp* and ToM coordinate to cobalt(II in a tridentate fashion when the bidentate ligand is the less hindered acetylacetonate. In crystal structures, the geometry of cobalt(II supported by the N3O2 donor set in the Tp* complex is a square-pyramid, whereas that in the ToM complex is close to a trigonal-bipyramid. Both Tp*- and ToM-acac complexes exhibit solvatochromic behavior, although the changing structural equilibria of these complexes in MeCN are quite different. In the bis(1-methylimidazol-2-ylmethylphenylborate (LPh complexes, Tp* retains the tridentate (к3 mode, whereas ToM functions as the bidentate (к2 ligand, giving the tetrahedral cobalt(II complex. The bowl-shaped cavity derived from the six methyl groups on ToM lead to susceptibility to the bulkiness of the opposite bidentate ligand. The entitled scorpionate compounds mediate hydrocarbon oxidation with organic peroxides. Allylic oxidation of cyclohexene occurs mainly on the reaction with tert-butyl hydroperoxide (TBHP, although the catalytic efficiency of the scorpionate ligand complexes is lower than that of Co(OAc2 and Co(acac2. On cyclohexane oxidation with meta-chloroperbenzoic acid (mCPBA, both ToM and Tp* complexes function as catalysts for hydroxylation. The higher electron-donating ToM complexes show faster initial reaction rates compared to the corresponding Tp* complexes.

The Application of Moessbauer Emission Spectroscopy to Industrial Cobalt Based Fischer-Tropsch Catalysts

International Nuclear Information System (INIS)

Loosdrecht, J. van de; Berge, P. J. van; Craje, M. W. J.; Kraan, A. M. van der

2002-01-01

The application of Moessbauer emission spectroscopy to study cobalt based Fischer-Tropsch catalysts for the gas-to-liquids process was investigated. It was shown that Moessbauer emission spectroscopy could be used to study the oxidation of cobalt as a deactivation mechanism of high loading cobalt based Fischer-Tropsch catalysts. Oxidation was observed under conditions that are in contradiction with the bulk cobalt phase thermodynamics. This can be explained by oxidation of small cobalt crystallites or by surface oxidation. The formation of re-reducible Co 3+ species was observed as well as the formation of irreducible Co 3+ and Co 2+ species that interact strongly with the alumina support. The formation of the different cobalt species depends on the oxidation conditions. Iron was used as a probe nuclide to investigate the cobalt catalyst preparation procedure. A high-pressure Moessbauer emission spectroscopy cell was designed and constructed, which creates the opportunity to study cobalt based Fischer-Tropsch catalysts under realistic synthesis conditions.

Plasma sprayed samarium--cobalt permanent magnets

International Nuclear Information System (INIS)

Willson, M.C.; Janowiecki, R.J.

1975-01-01

Samarium--cobalt permanent magnets were fabricated by arc plasma spraying. This process involves the injection of relatively coarse powder particles into a high-temperature gas for melting and spraying onto a substrate. The technique is being investigated as an economical method for fabricating cobalt--rare earth magnets for advanced traveling wave tubes and cross-field amplifiers. Plasma spraying permits deposition of material at high rates over large areas with optional direct bonding to the substrate, and offers the ability to fabricate magnets in a variety of shapes and sizes. Isotropic magnets were produced with high coercivity and good reproducibility in magnetic properties. Post-spray thermal treatments were used to enhance the magnetic properties of sprayed deposits. Samarium--cobalt magnets, sprayed from samarium-rich powder and subjected to post-spray heat treatment, displayed energy products in excess of 9 million gauss-oersteds and coercive forces of approximately 6000 oersteds. Bar magnet arrays were constructed by depositing magnets on ceramic substrates. (auth)

The cobalt radioactive isotopes in environment

International Nuclear Information System (INIS)

2007-01-01

For the year 1993 the total activity released in cobalt is 69 GBq for the whole of nuclear power plants. The part of activity in cobalt for La Hague in 1993 is 8 GBq of 58 Co and 2 GBq of 60 Co. The radioactive isotopes released by nuclear power plants or the reprocessing plant of La Hague under liquid effluents are shared by half between 58 Co and 60 Co. The exposure to sealed sources is the most important risk for the cobalt. The risk of acute exposure can associate a local irradiation of several decades of grays inducing a radiological burns, deep burn to treat in surgery by resection or graft even amputation. A global irradiation of organism for several grays induces an acute irradiation syndrome, often serious. At long term the stochastic effects are represented by leukemia and radio-induced cancers. The increase of probability of their occurrence is 1% by sievert. We must remind that the natural spontaneous probability is 25%. (N.C.)

Calculation support for industrial production of cobalt-60 at Leningrad NPP

International Nuclear Information System (INIS)

Artemov, Vladimir; Elshin, Alexander; Ivanov, Alexander; Gorbunov, Evgeny; Ikonnikov, Roman; Pimenov, Alexander

2008-01-01

Cobalt-60 is industrially produced at the Leningrad NPP by irradiation of cobalt-59 in special-purpose facilities loaded into the RBMK reactor core (all 4 units). The paper describes calculation methods used to determine the current activity of cobalt in irradiation assemblies for their timely unloading. The described peculiarities of core calculation model account for continuous refueling, overloading of irradiation assemblies and individual thermohydraulics in each channel under variation of reactor power. Fuel burnup in the core is calculated with a time step of about 24 hours. The resulting values for cobalt activity and uncertainties are presented in the paper as well. Deviation of calculated cobalt activity from measured activity is within the experimental accuracy of 10% (at confidence probability of 0.95). (authors)

Sorption behavior of cobalt on manganese dioxide, smectite and their mixture

International Nuclear Information System (INIS)

Ohnuki, T.; Kozai, N.

1995-01-01

The sorption behavior of cobalt on manganese dioxide, the clay mineral smectite and mixtures of the two was studied by batch type sorption/desorption experiments at neutral pH. Sorption behavior was examined by sequential extraction, in which the sorbents were contacted first with a 1 M CH 3 COONH 4 solution and then with a hydroxylamine solution (NH 2 OH of 1 M with 25 weight % CH 3 COOH). More than 70% of the sorbed cobalt was desorbed from smectite with a 1 M CH 3 COONH 4 solution: about 15% of the cobalt remained on the smectite after treatment with the hydroxylamine solution. Less than 1% of the remaining cobalt was desorbed from manganese dioxide with a 1 M CH 3 COONH 4 solution; with the hydroxylamine solution, all was desorbed. In mixtures of MnO 2 and smectite that were formulated to sorb equal amounts of cobalt regardless of the MnO 2 /smectite ratio in the mixture, less than 5% of the sorbed cobalt was desorbed by treatment with 1 M CH 3 COONH 4 . The fraction of the cobalt desorbed by treatment with the hydroxylamine solution increased with increased MnO 2 in the mixtures. The fraction of the cobalt sorbed on MnO 2 in the mixture was estimated from the desorption experiments. The results showed that higher fractions were sorbed onto MnO 2 than were estimated by the weighted averages of distribution coefficients for MnO 2 and smectite. Therefore, in minerals of the mixture, manganese dioxide is a more important component than smectite for the sorption of cobalt. (orig.)

A XANES study of cobalt speciation state in blue-and-white glazes from 16th to 17th century Chinese porcelains

Energy Technology Data Exchange (ETDEWEB)

Figueiredo, M.O., E-mail: ondina.figueiredo@lneg.pt [CENIMAT/I3N, Faculty Sciences and Technology, New University of Lisbon, Campus da Caparica, 2829-516 Caparica (Portugal); National Laboratory of Energy and Geology (LNEG), Apartado 7586, 2721-866 Alfragide (Portugal); Silva, T.P. [National Laboratory of Energy and Geology (LNEG), Apartado 7586, 2721-866 Alfragide (Portugal); CENIMAT/I3N, Faculty Sciences and Technology, New University of Lisbon, Campus da Caparica, 2829-516 Caparica (Portugal); Veiga, J.P. [CENIMAT/I3N, Faculty Sciences and Technology, New University of Lisbon, Campus da Caparica, 2829-516 Caparica (Portugal)

2012-04-15

Highlights: Black-Right-Pointing-Pointer Speciation of cobalt in ancient Chinese porcelain glazes studied by X-ray absorption near-edge spectroscopy. Black-Right-Pointing-Pointer Blue pigmenting role of tetrahedral Co{sup 2+} ions. Black-Right-Pointing-Pointer Uncertainties in deducing a formal valence state for cobalt ions from the edge energy. - Abstract: The composition of cobalt blue pigments used in ancient blue-and-white Chinese glazes is known to have changed between the 14th and the 17th century and ratios of some main chemical components plus trace elements are relevant guide-lines to establish the porcelain manufacture period. Once archaeological findings of Chinese porcelains can contribute to set up dating processes, a study of blue-and-white porcelain shards recovered during recent excavations in Lisbon Old-City was carried out by non-destructive laboratory X-ray fluorescence spectrometry for chemical characterization, combined with X-ray absorption spectroscopy (XAS) using synchrotron radiation to ascertain the formal valence and coordination of pigmenting cobalt ions. Following a preliminary extended X-ray absorption fine-structure study that revealed a coordination of divalent cobalt ions slightly above four, a detailed analysis of the near-edge region of Co 1s X-ray absorption spectra (XANES) was carried out on the blue-and-white glazes from those archaeological Chinese porcelain fragments. Pre-edge features and edge details are discussed in comparison with XANES spectra obtained from model compounds with well known crystal structure - Co{sub 3}O{sub 4}, CoAl{sub 2}O{sub 4} and Co{sub 2}SiO{sub 4}, plus a cobalt-based blue pigment (cerulean). Present chemical data validate the manufacture period of studied Chinese porcelains advanced by Art Historians on the single basis of stylistic features (late 16th and medium 17th century). Spectroscopic results confirm a coordination environment of pigmenting Co{sup 2+} ions close to tetrahedral and

A XANES study of cobalt speciation state in blue-and-white glazes from 16th to 17th century Chinese porcelains

International Nuclear Information System (INIS)

Figueiredo, M.O.; Silva, T.P.; Veiga, J.P.

2012-01-01

Highlights: ► Speciation of cobalt in ancient Chinese porcelain glazes studied by X-ray absorption near-edge spectroscopy. ► Blue pigmenting role of tetrahedral Co 2+ ions. ► Uncertainties in deducing a formal valence state for cobalt ions from the edge energy. - Abstract: The composition of cobalt blue pigments used in ancient blue-and-white Chinese glazes is known to have changed between the 14th and the 17th century and ratios of some main chemical components plus trace elements are relevant guide-lines to establish the porcelain manufacture period. Once archaeological findings of Chinese porcelains can contribute to set up dating processes, a study of blue-and-white porcelain shards recovered during recent excavations in Lisbon Old-City was carried out by non-destructive laboratory X-ray fluorescence spectrometry for chemical characterization, combined with X-ray absorption spectroscopy (XAS) using synchrotron radiation to ascertain the formal valence and coordination of pigmenting cobalt ions. Following a preliminary extended X-ray absorption fine-structure study that revealed a coordination of divalent cobalt ions slightly above four, a detailed analysis of the near-edge region of Co 1s X-ray absorption spectra (XANES) was carried out on the blue-and-white glazes from those archaeological Chinese porcelain fragments. Pre-edge features and edge details are discussed in comparison with XANES spectra obtained from model compounds with well known crystal structure – Co 3 O 4 , CoAl 2 O 4 and Co 2 SiO 4 , plus a cobalt-based blue pigment (cerulean). Present chemical data validate the manufacture period of studied Chinese porcelains advanced by Art Historians on the single basis of stylistic features (late 16th and medium 17th century). Spectroscopic results confirm a coordination environment of pigmenting Co 2+ ions close to tetrahedral and substantiate the dual role of cobalt as network former plus modifier in the glaze of ancient Chinese porcelains.

Concentration of radioactive cobalt by seaweeds in the food chain

International Nuclear Information System (INIS)

Nakahara, Motokazu; Koyanagi, Taku; Saiki, Masamichi

1976-01-01

On the pathway of radioactive substances in marine environments, seaweeds play an important role because of their higher concentration factors for many radionuclides and because they constitute a link of food chain in the sea. In the present work, uptake, distribution and excretion of radioactive cobalt were studied on several kinds of seaweeds by radioisotope tracer experiments under laboratory conditions and concentration factors were calculated. The concentration factors were also estimated from the results of stable cobalt determination by activation analysis or atomic absorption spectrometry on seaweeds and seawater, and compared with the results of tracer expts. The seaweeds showed the species specificity for the concentration of stable and radioactive cobalt with diverse values of concentration factors and biological half-lives. The transfer of radioactive cobalt in the food chain from contaminated seaweeds to mollusca was examined by feeding abalones, Haliotis discus, with four kinds of seaweed labelled with 60 Co and observing retention. Absorption rate for radioactive cobalt by abalones calculated at two days after feeding showed diverse values depending upon the species of seaweed, as follows: 47% through Laminaria japonica and Ulva pertusa, 31% through Undaria pinnatifida and 26 through Eisenia bicyclis, respectively. From the results, it was assumed that the accumulation of radioactive cobalt by mollusca is affected by the species of seaweeds as food. A very high concentration of ingested radioactive cobalt in the midgut gland was seen on the autoradiograph of abalone samples. (auth.)

Concentration of radioactive cobalt by seaweeds in the food chain

International Nuclear Information System (INIS)

Nakahara, M.; Koyanagi, T.; Saiki, M.

1975-01-01

On the pathway of radioactive substances in marine environments, seaweeds play an important role because of their higher concentration factors for many radionuclides and because they constitute a link in the food chain. In the present work, uptake, distribution and excretion of radioactive cobalt were studied on several kinds of seaweeds by radioisotope tracer experiments under laboratory conditions and concentration factors were calculated. The concentration factors were also estimated from the results of stable cobalt determination by activation analysis or atomic absorption spectrometry on seaweeds and seawater, and compared with the results of tracer experiments. The seaweeds showed the species specificity for the concentration of stable and radioactive cobalt with diverse values of concentration factors and biological half-lives. The transfer of radioactive cobalt in the food chain from contaminated seaweeds to mollusca was examined by feeding abalones, Haliotis discus, with four kinds of seaweed labelled with 60 Co and observing retention. Absorption rate for radioactive cobalt by abalones calculated at two days after feeding showed diverse values depending upon the species of seaweed, as follows: 47% through Laminaria japonica and Ulva pertusa, 31% through Undaria pinnatifida and 26% through Eisenia bicyclis, respectively. From the results, it was assumed that the accumulation of radioactive cobalt by mollusca is affected by the species of seaweeds as food. A very high concentration of ingested radioactive cobalt in the midgut gland was seen on the autoradiograph of abalone samples. (author)

Crystal structure of the Ce2Ni2Zn15 compound

International Nuclear Information System (INIS)

Opainich, I.M.; Pavlyuk, V.V.; Bodak, O.I.; Cherny, R.; Yvon, K.

1996-01-01

A structure of a new ternary compound of the composition Ce2Ni2Zn15 (sp.gr.R3-barm,a=0.9080(3) nm, c=1.3294(3) nm) was determined on single-crystal and powder specimens. The study was performed on a Philips PW1100 automatic diffractometer and a DRON-4.07 powder diffractometer. The Ce2Ni2Zn15 compound is crystallized in the Ce2Al2Co15 structure type with the aluminum positions being occupied by nickel and cobalt positions being occupied by zinc

Chemical bonding and magnetic properties of gadolinium (Gd) substituted cobalt ferrite

International Nuclear Information System (INIS)

Puli, Venkata Sreenivas; Adireddy, Shiva; Ramana, C.V.

2015-01-01

Graphical abstract: Room temperature Raman spectra of CoFe 2−x Gd x O 4 (CFGO, x = 0.0–0.3) compounds as a function of wavenumber (cm −1 ). - Highlights: • Gd substituted ferrites were synthesized under controlled concentration. • Gd ion induced lattice dynamical changes are significant. • Enhanced magnetization is observed upon Gd-incorporation in cobalt ferrite. • A correlation between lattice dynamics and magnetic properties is established. - Abstract: Polycrystalline gadolinium (Gd) substituted cobalt ferrites (CoFe 2−x Gd x O 4 ; x = 0–0.3, referred to CFGO) ceramics have been synthesized by solid state reaction method. Chemical bonding, crystal structure and magnetic properties of CFGO compounds have been evaluated as a function of Gd-content. X-ray diffraction (XRD) and Raman spectroscopic analyses confirmed the formation of inverse spinel cubic structure. However, a secondary ortho-ferrite phase (GdFeO 3 ) nucleates for higher values of Gd-content. A considerable increase in the saturation magnetization has been observed upon the initial substitution of Gd (x = 0.1). The saturation magnetization drastically decreases at higher Gd content (x ⩾ 0.3). No contribution from ortho-ferrite GdFeO 3 phase is noted to the magnetic properties. The increase in the magnetic saturation magnetization is attributed to the higher magnetic moment of Gd 3+ (4f 7 ) residing in octahedral sites is higher when compared to that of Fe 3+ (3d 5 ) and as well due to the migration of Co 2+ (3d 7 ) ions from the octahedral to the tetrahedral sites with a magnetic moment aligned anti-parallel to those of rare earth (RE 3+ ) ions in the spinel lattice. Increase in coercivity with increase in Gd 3+ is content is attributed to magnetic anisotropy in the ceramics

PENYERAPAN COBALT-60 DARI AIR OLEH TANAMAN KIAPU (Pistia stratiotes L.)

OpenAIRE

Lailatul Nuzzulul Safitri; Poppy Intan Tjahaja; Ida Bagus Made Suryatika

2015-01-01

Has conducted research Cobalt-60 radionuclide uptake by plants kiapu (Pistia stratiotes L.) found in many waters. The purpose of the study was to determine the value of the transfer factor on plant kiapu to Cobalt-60 in water. The study was conducted by growing plants on media kiapu gutter water in pots with the height 35 cm and diameter 11,5 cm containing Cobalt-60. The amount of Cobalt - 60 is absorbed and accumulated by the plant parts, i.e. roots and leaves, was observed by measuring the ...

The structural evolution and diffusion during the chemical transformation from cobalt to cobalt phosphide nanoparticles

KAUST Repository

Ha, Don-Hyung

2011-01-01

We report the structural evolution and the diffusion processes which occur during the phase transformation of nanoparticles (NPs), ε-Co to Co 2P to CoP, from a reaction with tri-n-octylphosphine (TOP). Extended X-ray absorption fine structure (EXAFS) investigations were used to elucidate the changes in the local structure of cobalt atoms which occur as the chemical transformation progresses. The lack of long-range order, spread in interatomic distances, and overall increase in mean-square disorder compared with bulk structure reveal the decrease in the NP\\'s structural order compared with bulk structure, which contributes to their deviation from bulk-like behavior. Results from EXAFS show both the Co2P and CoP phases contain excess Co. Results from EXAFS, transmission electron microscopy, X-ray diffraction, and density functional theory calculations reveal that the inward diffusion of phosphorus is more favorable at the beginning of the transformation from ε-Co to Co2P by forming an amorphous Co-P shell, while retaining a crystalline cobalt core. When the major phase of the sample turns to Co 2P, the diffusion processes reverse and cobalt atom out-diffusion is favored, leaving a hollow void, characteristic of the nanoscale Kirkendall effect. For the transformation from Co2P to CoP theory predicts an outward diffusion of cobalt while the anion lattice remains intact. In real samples, however, the Co-rich nanoparticles continue Kirkendall hollowing. Knowledge about the transformation method and structural properties provides a means to tailor the synthesis and composition of the NPs to facilitate their use in applications. © 2011 The Royal Society of Chemistry.

Development of hierarchically porous cobalt oxide for enhanced photo-oxidation of indoor pollutants

Energy Technology Data Exchange (ETDEWEB)

Cheng, J. P., E-mail: chengjp@zju.edu.cn [Zhejiang University, State Key Laboratory of Silicon Materials, Department of Materials Science and Engineering (China); Shereef, Anas; Gray, Kimberly A., E-mail: k-gray@northwestern.edu [Northwestern University, Center for Catalysis and Surface Science (United States); Wu, Jinsong [Northwestern University, Department of Materials Science and Engineering (United States)

2015-03-15

Porous cobalt oxide was successfully prepared by precipitation of cobalt hydroxide followed by low temperature thermal decomposition. The morphologies of the resultant oxides remained as the corresponding hydroxides, although the morphology of cobalt hydroxides was greatly influenced by the precursor salts. The cobalt oxides with average crystal size less than 20 nm were characterized by X-ray diffraction, scanning electron microscope, BET surface area, and XPS analysis. The photocatalytic activities of the various cobalt oxides morphologies were investigated by comparing the photo-degradation of acetaldehyde under simulated solar illumination. Relative to their low order structures and reference titania samples, the hierarchical nanostructures of cobalt oxide showed excellent abilities to rapidly degrade acetaldehyde, a model air pollutant. This was attributed to the unique nature of these hierarchical cobalt oxide nanoassemblies, which contained many catalytically active reaction sites and open pores.

Substoichiometric cobalt oxide monolayer on Ir(100)-(1 x 1)

International Nuclear Information System (INIS)

Gubo, M; Ebensperger, C; Meyer, W; Hammer, L; Heinz, K

2009-01-01

A substoichiometric monolayer of cobalt oxide has been prepared by deposition and oxidation of slightly less than one monolayer of cobalt on the unreconstructed surface of Ir(100). The ultrathin film was investigated by scanning tunnelling microscopy (STM) and quantitative low-energy electron diffraction (LEED). The cobalt species of the film reside in or near hollow positions of the substrate with, however, unoccupied sites (vacancies) in a 3 x 3 arrangement. In the so-formed 3 x 3 supercell the oxide's oxygen species are both threefold and fourfold coordinated to cobalt, forming pyramids with a triangular and square cobalt basis, respectively. These pyramids are the building blocks of the oxide. Due to the reduced coordination as compared to the sixfold one in the bulk of rock-salt-type CoO, the Co-O bond lengths are smaller than in the latter. For the threefold coordination they compare very well with the bond length in oxygen terminated CoO(111) films investigated recently. The substoichiometric 3 x 3 oxide monolayer phase transforms to a stoichiometric c(10 x 2)-periodic oxide monolayer under oxygen exposure, in which, however, cobalt and oxygen species are in (111) orientation and so form a CoO(111) layer.

Testing of cobalt-free alloys for valve applications using a special test loop

International Nuclear Information System (INIS)

Benhamou, C.

1992-01-01

Considering that use of cobalt alloys should be avoided as far as possible in PWR components, a programme aimed at establishing the performance of cobalt-free alloys has been performed for valve applications, where cobalt alloys are mainly used. Referring to past work, two types of cobalt-free alloys were selected: Ni-Cr-B-Si and Ni-Cr-Fe alloys. Cobalt-free valves' behaviour has been evaluated comparatively with cobalt valves by implementation of a programme in a special PWR test loop. At the issue of the loop test programme, which included endurance, thermal shock and erosion tests, cobalt-free alloys candidate to replace cobalt alloys are proposed in relation with valve type (globe valve and swing check valve). The following was established: (i) Colmonoy 4-26 (Ni-Cr-B-Si alloy) and Cenium Z20 (Ni-Cr-Fe alloy) deposited by plasma arc process were found suitable for use in 3inch swing check valves; (ii) for integral parts acting as guide rings, Nitronic 60 and Cesium Z20/698 were tested successfully; (iii) for small-bore components such as 2inch globe valves, no solution can yet be proposed; introduction of cobalt-free alloys is dependent on the development of automatic advanced arc surfacing techniques applied to small-bore components

Neutron diffraction studies on cobalt substituted BiFeO3

Science.gov (United States)

Ray, J.; Biswal, A. K.; Acharya, S.; Babu, P. D.; Siruguri, V.; Vishwakarma, P. N.

2013-02-01

A dilute concentration of single phase Cobalt substituted Bismuth ferrite, BiFe1-XCoXO3; (x=0, 0.02) is prepared by sol-gel auto combustion method. Room temperature neutron diffraction patterns show no change in the crystal and magnetic structure upon cobalt doping. The calculation of magnetic moments shows 3.848 μB for Fe+ and 2.85 μB for Co3+. The cobalt is found to be in intermediate spin state.

Trigonal Prismatic Tris-pyridineoximate Transition Metal Complexes: A Cobalt(II) Compound with High Magnetic Anisotropy.

Science.gov (United States)

Pavlov, Alexander A; Savkina, Svetlana A; Belov, Alexander S; Nelyubina, Yulia V; Efimov, Nikolay N; Voloshin, Yan Z; Novikov, Valentin V

2017-06-19

High magnetic anisotropy is a key property of paramagnetic shift tags, which are mostly studied by NMR spectroscopy, and of single molecule magnets, for which magnetometry is usually used. We successfully employed both these methods in analyzing magnetic properties of a series of transition metal complexes, the so-called clathrochelates. A cobalt complex was found to be both a promising paramagnetic shift tag and a single molecule magnet because of it having large axial magnetic susceptibility tensor anisotropy at room temperature (22.5 × 10 -32 m 3 mol -1 ) and a high effective barrier to magnetization reversal (up to 70.5 cm -1 ). The origin of this large magnetic anisotropy is a negative value of zero-field splitting energy that reaches -86 cm -1 according to magnetometry and NMR measurements.

Construction of an apparatus for nuclear orientation measurements at low temperatures. Application to neodymium-cobalt alloy; Realisation d'un appareil pour des mesures d'orientation nucleaire a basse temperature. Application a l'alliage neodyme-cobalt

Energy Technology Data Exchange (ETDEWEB)

Mayer, E [Commissariat a l' Energie Atomique, Grenoble (France). Centre d' Etudes Nucleaires

1965-10-01

We describe experiments along which has been studied the anisotropy of {gamma} radiations emitted by oriented nuclei. We have used the great hyperfine fields acting on nuclei in ferromagnetic metals so as to produce alignment at low temperature. By irradiation we obtained a few cobalt 60 nuclei in our samples which were then cooled down to 0,01 K. The anisotropic rate of the 1,33 MeV {gamma} radiation was measured in function of the sample temperature, using as thermometer the anisotropy of {gamma} radiation emitted by cobalt 60 nuclei in a cobalt single crystal. Cobalt 60 was lined up in a cobalt nickel alloy (40% Ni). The hyperfine field at the cobalt was measured compared to the effective field in metallic cobalt: Heff(Co Ni)/Heff(Co metal) = 0.71 {+-} 0.12. These results are in good agreement with specific heat measurements made previously. Cobalt 60 has been polarised in a neodymium-cobalt alloy (NdCo{sub 5}). The field at the cobalt in NdCo{sub 5} has been measured compared to the field in metallic cobalt and taking the non-saturation into account we found 165000 oersteds < Heff(NdCo{sub 5}) < 220000 oersteds. (author) [French] Nous decrivons des experiences au cours desquelles nous avons etudie l'anisotropie de rayonnements {gamma} emis par des noyaux orientes. Nous avons utilise les grands champs hyperfins agissant sur las noyaux dans les metaux ferromagnetiques pour produire l'alignement a basse temperature. Par irradiation nous avons obtenu quelques noyaux de cobalt 60 dans nos echantillons qui furent ensuite refroidis a 0,01 K. Le degre d'anisotropie du rayonnement {gamma} de 1,33 MeV fut mesure en fonction de la temperature de l'echantillon en utilisant l'anisotropie du rayonnement {gamma} de noyaux de cobalt 60 dans un monocristal de cobalt metallique utilise comme thermometre. Le cobalt 60 a ete aligne dans un alliage de cobalt-nickel (40% Ni). Le champ hyperfin au niveau du cobalt a ete mesure par rapport au champ effectif dans le cobalt metallique

Titanium oxide modification with oxides of mixed cobalt valence for photo catalysis

International Nuclear Information System (INIS)

Alanis O, R.; Jimenez B, J.

2010-01-01

In the present work, heterogenous photo catalysis, a technique often used for organic compound degradation toxic in water, was used. The photo catalyst most often used in this technique is TiO 2 , which due to its physical and chemical properties, can degrade a great number of organic compounds. In addition, in recent years it has been verified that the doping of semiconductors with metals or metallic oxides increases the photo catalytic activity of these semiconductors, which is why it was proposed for doping by the impregnating method using commercial TiO 2 synthesized by the Degussa company (TiO 2 Degussa P25) with and oxide of mixed cobalt valence (Co 3 O 4 ) synthesized using the sol-gel method. The synthesized photo catalyst TiO 2 /Co 3 O 4 was characterized by the techniques of X-ray diffraction, scanning electronic microscopy, Raman spectroscopy and finally, photo catalytic tests by means of the degradation of methylene blue. (Author)

Bioactivity and mechanical behaviour of cobalt oxide-doped ...

Indian Academy of Sciences (India)

tive base glass and cobalt oxide-doped glass were prepared by the addition of cobalt oxide (0, ... and 1 N HCl at 37. ◦. C as compared with the ... SO2−. 4. Cl. −. Simulated body fluid. 142.0. 5.0. 1.5. 2.5. 4.2. 1.0. 0.5. 147.8. Human blood plasma ...

Cobalt production in RAPS-1

International Nuclear Information System (INIS)

Krishnan, P.D.; Purandare, H.D.

1978-01-01

At present in RAPS-1 radioisotope Co 60 is produced by irradiating Co 59 in the adjusters which perform the function of regulation of reactivity, power and xenon override. But the manrem expenditure of the crew handling the charge and discharge of the adjusters is going to be prohibitively high. It is therefore proposed to irradiate Co 59 in the fuel channel positions. The physics optimisation study for such irradiation is presented. The burnup penalty and loss of power are estimated to produce the required quantity of Co 60 after optimising the number of cobalt pencils in a bundle and the positions of the cobalt producing channels in the reactor core. (author)

Nickel and cobalt bimetallic hydroxide catalysts for urea electro-oxidation

International Nuclear Information System (INIS)

Yan Wei; Wang Dan; Botte, Gerardine G.

2012-01-01

Nickel–Cobalt bimetallic hydroxide electrocatalysts, synthesized through a one-step electrodeposition method, were evaluated for the oxidation of urea in alkaline conditions with the intention of reducing the oxidation overpotential for this reaction. The Nickel–Cobalt bimetallic hydroxide catalysts were characterized by scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDXS), Raman spectroscopy, cyclic voltammetry (CV), and polarization techniques. A significant reduction in the overpotential (150 mV) of the reaction was observed with the Nickel–Cobalt bimetallic hydroxide electrode (ca. 43% Co content) when compared to a nickel hydroxide electrode. The decrease of the urea oxidation potential on the Nickel–Cobalt bimetallic hydroxide electrodes reveals great potential for future applications of urea electro-oxidation, including wastewater remediation, hydrogen production, sensors, and fuel cells.

Hydrogen evolution catalyzed by cobalt diimine-dioxime complexes.

Science.gov (United States)

Kaeffer, Nicolas; Chavarot-Kerlidou, Murielle; Artero, Vincent

2015-05-19

Mimicking photosynthesis and producing solar fuels is an appealing way to store the huge amount of renewable energy from the sun in a durable and sustainable way. Hydrogen production through water splitting has been set as a first-ranking target for artificial photosynthesis. Pursuing that goal requires the development of efficient and stable catalytic systems, only based on earth abundant elements, for the reduction of protons from water to molecular hydrogen. Cobalt complexes based on glyoxime ligands, called cobaloximes, emerged 10 years ago as a first generation of such catalysts. They are now widely utilized for the construction of photocatalytic systems for hydrogen evolution. In this Account, we describe our contribution to the development of a second generation of catalysts, cobalt diimine-dioxime complexes. While displaying similar catalytic activities as cobaloximes, these catalysts prove more stable against hydrolysis under strongly acidic conditions thanks to the tetradentate nature of the diimine-dioxime ligand. Importantly, H2 evolution proceeds via proton-coupled electron transfer steps involving the oxime bridge as a protonation site, reproducing the mechanism at play in the active sites of hydrogenase enzymes. This feature allows H2 to be evolved at modest overpotentials, that is, close to the thermodynamic equilibrium over a wide range of acid-base conditions in nonaqueous solutions. Derivatization of the diimine-dioxime ligand at the hydrocarbon chain linking the two imine functions enables the covalent grafting of the complex onto electrode surfaces in a more convenient manner than for the parent bis-bidentate cobaloximes. Accordingly, we attached diimine-dioxime cobalt catalysts onto carbon nanotubes and demonstrated the catalytic activity of the resulting molecular-based electrode for hydrogen evolution from aqueous acetate buffer. The stability of immobilized catalysts was found to be orders of magnitude higher than that of catalysts in the

Sintered cobalt-rare earth intermetallic product

International Nuclear Information System (INIS)

Benz, M.C.

1975-01-01

A process is described for preparing novel sintered cobalt--rare earth intermetallic products which can be magnetized to form permanent magnets having stable improved magnetic properties. A cobalt--rare earth metal alloy is formed having a composition which at sintering temperature falls outside the composition covered by the single Co 5 R intermetallic phase on the rare earth richer side. The alloy contains a major amount of the Co 5 R intermetallic phase and a second solid CoR phase which is richer in rare earth metal content than the Co 5 R phase. The specific cobalt and rare earth metal content of the alloy is substantially the same as that desired in the sintered product. The alloy, in particulate form, is pressed into compacts and sintered to the desired density. The sintered product is comprised of a major amount of the Co 5 R solid intermetallic phase and up to about 35 percent of the product of the second solid CoR intermetallic phase which is richer in rare earth metal content than the Co 5 R phase

Hot corrosion of low cobalt alloys

Science.gov (United States)

Stearns, C. A.

1982-01-01

The hot corrosion attack susceptibility of various alloys as a function of strategic materials content are investigated. Preliminary results were obtained for two commercial alloys, UDIMET 700 and Mar-M 247, that were modified by varying the cobalt content. For both alloys the cobalt content was reduced in steps to zero. Nickel content was increased accordingly to make up for the reduced cobalt but all other constituents were held constant. Wedge bar test samples were produced by casting. The hot corrosion test consisted of cyclically exposing samples to the high velocity flow of combustion products from an air-fuel burner fueled with jet A-1 and seeded with a sodium chloride aqueous solution. The flow velocity was Mach 0.5 and the sodium level was maintained at 0.5 ppm in terms of fuel plus air. The test cycle consisted of holding the test samples at 900 C for 1 hour followed by 3 minutes in which the sample could cool to room temperature in an ambient temperature air stream.

EFTF cobalt test assembly results

International Nuclear Information System (INIS)

Rawlins, J.A.; Wootan, D.W.; Carter, L.L.; Brager, H.R.; Schenter, R.E.

1988-01-01

A cobalt test assembly containing yttrium hydride pins for neutron moderation was irradiated in the Fast Flux Test Facility during Cycle 9A for 137.7 equivalent full power days at a power level fo 291 MW. The 36 test pins consisted of a batch of 32 pins containing cobalt metal to produce Co-60, and a set of 4 pins with europium oxide to produce Gd-153, a radioisotope used in detection of the bone disease Osteoporosis. Post-irradiation examination of the cobalt pins determined the Co-60 produced with an accuracy of about 5 %. The measured Co-60 spatially distributed concentrations were within 20 % of the calculated concentrations. The assembly average Co-60 measured activity was 4 % less than the calculated value. The europium oxide pins were gamma scanned for the europium isotopes Eu-152 and Eu-154 to an absolute accuracy of about 10 %. The measured europium radioisotpe anc Gd-153 concentrations were within 20 % of calculated values. In conclusion, the hydride assembly performed well and is an excellent vehicle for many Fast Flux Test Facility isotope production applications. The results also demonstrate that the calculational methods developed by the Westinghouse Hanford Company are very accurate. (author)

Effect of Cobalt Supplementation on Performance of growing Calves

Directory of Open Access Journals (Sweden)

V.Nagabhushana

Full Text Available The experiment was conducted to study the effect of critical supplementation of wheat straw with cobalt on fibre utilization and nutrient utilization in growing cross-bred male calves. Twenty-one crossbred (HF X Local male growing calves of 3-4 months age were fed with wheat straw based diet consisting without (Co0 and with 1 (Co1 and 6 (Co6 ppm cobalt as cobaltous chloride. There was no significant difference in intake of wheat straw, concentrate and DMI between the three groups and the ratio between concentrate and wheat straw was maintained at 40:60 irrespective of dietary level of cobalt. Similarly, average cumulative body weight, net gain in body weight or feed efficiency did not differ significantly between treatments. No significant effect was observed on the digestibility of dry matter, organic matter, crude protein, ether extract and fibre constituents like NDF, ADF, hemicellulose or cellulose by supplementation of 1 and 6 ppm Co to the diet of growing calves. Balance of nutrients such as Nitrogen, Calcium and Phosphorus was similar and positive in all the treatment groups. TDN and DCP values of the experimental diets remained almost similar irrespective of dietary level of cobalt. [Veterinary World 2008; 1(10.000: 299-302

Cobalt bis(dicarbollides)(1-) covalently attached to the calyx[4]arene platform: the first combination of organic bowl-shaped matrices and inorganic metallaborane cluster anions

NARCIS (Netherlands)

Grüner, Bohumír; Mikulasek, Libor; Baca, Jirí; Cisarova, Ivana; Böhmer, Volker; Danila, Crenguta; Reinoso garcia, M.M.; Verboom, Willem; Reinhoudt, David; Casnati, Alessandro; Ungaro, Rocco

2005-01-01

Various calix[4]arene and resorc[4]arene ionic compounds substituted by cobalt bis(dicarbollide) anions (1) have been prepared for the first time. From tBu-calix[4]arene (A) the complete series of mono-, di-, tri- and tetrasubstituted derivatives bearing one to four cluster anions on the lower rim

In situ fabrication and characterization of cobalt ferrite nanorods/graphene composites

International Nuclear Information System (INIS)

Fu, Min; Jiao, Qingze; Zhao, Yun

2013-01-01

Cobalt ferrite nanorods/graphene composites were prepared by a one-step hydrothermal process using NaHSO 3 as the reducing agent and 1-propyl-3-hexadecylimidazolium bromide as the structure growth-directing template. The reduction of graphene oxide and the in situ formation of cobalt ferrite nanorods were accomplished in a one-step reaction. The structure and morphology of as-obtained composites were characterized by field emission scanning electron microscopy, transmission electron microscopy, high resolution transmission electron microscopy, atomic force microscope, X-ray diffractometer, Fourier transform infrared spectra, X-ray photoelectron spectroscopy and Raman spectroscopy. Uniform rod-like cobalt ferrites with diameters of about 100 nm and length of about 800 nm were homogeneously distributed on the graphene sheets. The hybrid materials showed a saturation magnetization of 42.5 emu/g and coercivity of 495.1 Oe at room temperature. The electromagnetic parameters were measured using a vector network analyzer. A minimum reflection loss (RL) of − 25.8 dB was observed at 16.1 GHz for the cobalt ferrite nanorods/graphene composites with a thickness of 2 mm, and the effective absorption frequency (RL < − 10 dB) ranged from 13.5 to 18.0 GHz. The composites exhibited better absorbing properties than the cobalt ferrite nanorods and the mixture of cobalt ferrite nanorods and graphene. - Highlights: • Reduction of GO and formation of ferrites were accomplished in a one-step reaction. • Ionic liquid was used to control 1D growth of ferrite nanorods for the first time. • Cobalt ferrite nanorods/graphene composites showed dielectric and magnetic loss. • Cobalt ferrite nanorods/graphene composites exhibited better absorbing properties

Radioactive and stable cobalt concentrations in mussel in Kyushu island, Japan

International Nuclear Information System (INIS)

Momoshima, Noriyuki; Shiki, Atsushi; Takashima, Yoshimasa; Maki, Takao; Koriyama, Munehiro; Shimozono, Seika; Imamura, Hiroka; Nakamata, Kojiro.

1985-01-01

Two kinds of mussel, Septifer virgatus and Mytilus edulis, were collected from Kyushu island, Japan, in order to elucidate a background level of 60 Co, which is one of the most significant radionuclide for environmental monitoring around a nuclear power plant. The mussels were collected from 7 locations in 1983 and classified 2 or 3 groups depending on their shell size at each location. Activities of 60 Co were measured by a low-background β counter after purified by means of chemical separation and electrodeposition. Stable cobalt concentrations were determined by colorimetric method. The concentrations of cobalt in Septifer virgatus are one order higher level than that in Mytilus edulis. There are not so large difference in cobalt content depending on shell size so long as comparing them at the same location. The radioactivities in mussels show the same trend as stable cobalt. It has become apparent that Septifer virgatus has a tendency to concentrate cobalt with growing but Mytilus edulis is opposite. The cobalt-60 introduced to sea from nuclear explosions seems to be relatively constant in coastal seawater since specific activities are distributed in a narrow range in spite of kind, shell size and location. (author)

Copolymerisation of Propylene Oxide and Carbon Dioxide by Dinuclear Cobalt Porphyrins

KAUST Repository

Anderson, Carly E.; Vagin, Sergei I.; Hammann, Markus; Zimmermann, Leander; Rieger, Bernhard

2013-01-01

Two dinuclear cobalt porphyrins comprising different structural tethering motifs at the porphyrin periphery were synthesised, along with a representative mononuclear cobalt porphyrin, and their catalytic activities tested towards carbon dioxide-propylene oxide copolymerisation in the presence of bis(triphenylphosphoranyl)ammonium chloride cocatalyst. The catalytic activities of the mononuclear and the bis-para-tethered dinuclear cobalt porphyrin with selective formation of poly(propylene carbonate) are largely comparable, showing no benefit of dinuclearity in contrast to the case of cobalt salen complexes and suggesting that polymer growth proceeds exclusively from one metal centre. The alternative bis-ortho-tethered porphyrin demonstrated considerably reduced activity, with dominant formation of cyclic propylene carbonate, as a result of hindered substrate approach at the metal centre. Time-resolved UV/Vis spectroscopic studies suggested a general intolerance of the cobalt(III) porphyrin catalysts towards the copolymerisation conditions in the absence of carbon dioxide pressure, leading to catalytically inactive cobalt(II) species. In the presence of carbon dioxide, the bis-ortho-tethered catalyst showed the fastest deactivation, which is related to an unfavourable steric arrangement of the linker fragment, as was also confirmed by NMR spectroscopic measurements. © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Copolymerisation of Propylene Oxide and Carbon Dioxide by Dinuclear Cobalt Porphyrins

KAUST Repository

Anderson, Carly E.

2013-09-18

Two dinuclear cobalt porphyrins comprising different structural tethering motifs at the porphyrin periphery were synthesised, along with a representative mononuclear cobalt porphyrin, and their catalytic activities tested towards carbon dioxide-propylene oxide copolymerisation in the presence of bis(triphenylphosphoranyl)ammonium chloride cocatalyst. The catalytic activities of the mononuclear and the bis-para-tethered dinuclear cobalt porphyrin with selective formation of poly(propylene carbonate) are largely comparable, showing no benefit of dinuclearity in contrast to the case of cobalt salen complexes and suggesting that polymer growth proceeds exclusively from one metal centre. The alternative bis-ortho-tethered porphyrin demonstrated considerably reduced activity, with dominant formation of cyclic propylene carbonate, as a result of hindered substrate approach at the metal centre. Time-resolved UV/Vis spectroscopic studies suggested a general intolerance of the cobalt(III) porphyrin catalysts towards the copolymerisation conditions in the absence of carbon dioxide pressure, leading to catalytically inactive cobalt(II) species. In the presence of carbon dioxide, the bis-ortho-tethered catalyst showed the fastest deactivation, which is related to an unfavourable steric arrangement of the linker fragment, as was also confirmed by NMR spectroscopic measurements. © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Smoothing an isolated interface of cobalt-copper under irradiation by low-energy argon ions

International Nuclear Information System (INIS)

Stognij, A.I.; Novitskij, N.N.; Stukalov, O.M.

2003-01-01

Multilayer film structures, i.e. gold layer-copper-cobalt, are considered. It is shown that the structure, where cobalt surface prior to copper layer deposition was subjected to additional irradiation by a flow of argon ions, features the smoothest surface. The conclusion is made about smoothing out of cobalt-copper interface as a result of multiple collisions of argon slow ions and cobalt atoms during braking within two or three upper atomic rows of the cobalt layer [ru

Cobalt dinitrosoalkane complexes in the C-H functionalization of olefins.

Science.gov (United States)

Schomaker, Jennifer M; Boyd, W Christopher; Stewart, Ian C; Toste, F Dean; Bergman, Robert G

2008-03-26

The use of cobalt dinitrosoalkane complexes in the C-H functionalization of alkenes has been demonstrated. Reaction of a series of alkenes with Me4CpCo(CO)2 in the presence of NO generates intermediate cobalt dinitrosoalkane complexes that can be deprotonated alpha to the nitrosyl group and added to various Michael acceptors. The resultant products can then undergo retrocycloaddition reactions in the presence of the original alkene to regenerate the starting cobalt dinitrosoalkane complex and release the functionalized alkene.

Li-ion battery recycling and cobalt flow analysis in Japan

OpenAIRE

Asari, Misuzu; Sakai, Shin-ichi

2013-01-01

Batteries sometimes contain precious or toxic substances (e.g. nickel, cobalt, lead, mercury, cadmium). However, the collection and recycling rate of small batteries were low in Japan.　We focus on cobalt in lithium ion (Li-ion) batteries and conduct chemical analysis, questioner survey and flow analysis in Japan.Results of chemical analysis showed that the concentration of cobalt in Li-ion batteries was around 20% regardless of the year manufactured or the manufacturer. As a result of the con...

Cobalt uptake and binding in human red blood cells

DEFF Research Database (Denmark)

Simonsen, Lars Ole; Brown, Anthony M; Harbak, Henrik

2011-01-01

of cobalt, and also from the initial slope of the cobalt buffering curve. The cobalt accumulation is similar in fed and ATP-depleted cells. The buffering curve for [Co(T)](c) can be fitted by a Michaelis type function with B(max)=24 mmol (l cells)(-1) and half-saturation at 240 µM [Co(2+)](c). The tracer...... reversibly bound, being releasable by excess extracellular EGTA in the presence of A23187, and partly tightly bound, remaining in the cells even at high ionophore concentrations. The tightly bound fraction builds up over time, and is larger and develops earlier in fed cells compared to ATP-depleted cells......-migrate with hemoglobin in Sephadex column chromatography of a lysate of (57)Co-loaded cells. (57)Co also co-migrates with hemoglobin when added to a lysate of unlabeled cells or to a solution of purified hemoglobin, in both cases with a time-dependent development of tight binding. Cobalt is known to bind to the globin...

Cobalt catalyzed hydroesterification of a wide range of olefins

Energy Technology Data Exchange (ETDEWEB)

Van Rensburg, H.; Hanton, M.; Tooze, R.P.; Foster, D.F. [Sasol Technology UK, St Andrews (United Kingdom)

2011-07-01

Petrochemical raw materials are an essential raw material for the production of detergents with a substantial portion of synthetic fatty alcohols being produced via hydroformylation of oil or coal derived olefins. Carbonylation processes other than hydroformylation have to date not been commercially employed for the production of fatty esters or alcohols. In this document we highlight the opportunities of converting olefins to esters using cobalt catalyzed alkoxycarbonylation. This process is highly versatile and applicable to a wide range of olefins, linear or branched, alpha or internal in combination with virtually any chain length primary or secondary alcohol allowing the synthesis of a diverse array of compounds such as ester ethoxylated surfactants, methyl branched detergents, lubricants and alkyl propanoates. Furthermore, alkoxycarbonylation of a broad olefin/paraffin hydrocarbon range could be used to produce the corresponding broad cut detergent alcohols. (orig.)

Self-subunit swapping occurs in another gene type of cobalt nitrile hydratase.

Directory of Open Access Journals (Sweden)

Yi Liu

Full Text Available Self-subunit swapping is one of the post-translational maturation of the cobalt-containing nitrile hydratase (Co-NHase family of enzymes. All of these NHases possess a gene organization of , which allows the activator protein to easily form a mediatory complex with the α-subunit of the NHase after translation. Here, we discovered that the incorporation of cobalt into another type of Co-NHase, with a gene organization of , was also dependent on self-subunit swapping. We successfully isolated a recombinant NHase activator protein (P14K of Pseudomonas putida NRRL-18668 by adding a Strep-tag N-terminal to the P14K gene. P14K was found to form a complex [α(StrepP14K(2] with the α-subunit of the NHase. The incorporation of cobalt into the NHase of P. putida was confirmed to be dependent on the α-subunit substitution between the cobalt-containing α(StrepP14K(2 and the cobalt-free NHase. Cobalt was inserted into cobalt-free α(StrepP14K(2 but not into cobalt-free NHase, suggesting that P14K functions not only as a self-subunit swapping chaperone but also as a metallochaperone. In addition, NHase from P. putida was also expressed by a mutant gene that was designed with a order. Our findings expand the general features of self-subunit swapping maturation.

Lump Kinetic Analysis of Syngas Composition Effect on Fischer-Tropsch Synthesis over Cobalt and Cobalt-Rhenium Alumina Supported Catalyst

Directory of Open Access Journals (Sweden)

Dewi Tristantini

2016-03-01

Received: 10th November 2015; Revised: 10th February 2016; Accepted: 16th February 2016 How to Cite: Tristantini, D., Suwignjo, R.K. (2016. Lump Kinetic Analysis of Syngas Composition Effect on Fischer-Tropsch Synthesis over Cobalt and Cobalt-Rhenium Alumina Supported Catalyst. Bulletin of Chemical Reaction Engineering & Catalysis, 11 (1: 84-92. (doi:10.9767/bcrec.11.1.424.84-92 Permalink/DOI: http://dx.doi.org/10.9767/bcrec.11.1.424.84-92

Photo release of nitrous oxide from the hyponitrite ion studied by infrared spectroscopy. Evidence for the generation of a cobalt-N2O complex. Experimental and DFT calculations.

Science.gov (United States)

Chacón Villalba, M Elizabeth; Franca, Carlos A; Güida, Jorge A

2017-04-05

The solid state photolysis of sodium, silver and thallium hyponitrite (M 2 N 2 O 2 , M=Na, Ag, Tl) salts and a binuclear complex of cobalt bridged by hyponitrite ([Co(NH 3 ) 5 -N(O)-NO-Co(NH 3 ) 5 ] 4+ ) were studied by irradiation with visible and UV light in the electronic absorption region. The UV-visible spectra for free hyponitrite ion and binuclear complex of cobalt were interpreted in terms of Density Functional Theory calculations in order to explain photolysis behavior. The photolysis of each compound depends selectively on the irradiation wavelength. Irradiation with 340-460nm light and with the 488nm laser line generates photolysis only in silver and thallium hyponitrite salts, while 253.7nm light photolyzed all the studied compounds. Infrared spectroscopy was used to follow the photolysis process and to identify the generated products. Remarkably, gaseous N 2 O was detected after photolysis in the infrared spectra of sodium, silver, and thallium hyponitrite KBr pellets. The spectra for [Co(NH 3 ) 5 -N(O)-NO-Co(NH 3 ) 5 ] 4+ suggest that one cobalt ion remains bonded to N 2 O from which the generation of a [(NH 3 ) 5 CoNNO] +3 complex is inferred. Density Functional Theory (DFT) based calculations confirm the stability of this last complex and provide the theoretical data which are used in the interpretation of the electronic spectra of the hyponitrite ion and the cobalt binuclear complex and thus in the elucidation of their photolysis behavior. Carbonate ion is also detected after photolysis in all studied compounds, presumably due to the reaction of atmospheric CO 2 with the microcrystal surface reaction products. Kinetic measurements for the photolysis of the binuclear complex suggest a first order law for the intensity decay of the hyponitrite IR bands and for the intensity increase in the N 2 O generation. Predicted and experimental data are in very good agreement. Copyright © 2017 Elsevier B.V. All rights reserved.

Tailoring the magnetic properties of cobalt-ferrite nanoclusters

Energy Technology Data Exchange (ETDEWEB)

Vega, A. Estrada de la; Garza-Navarro, M. A., E-mail: marco.garzanr@uanl.edu.mx; Durán-Guerrero, J. G.; Moreno Cortez, I. E.; Lucio-Porto, R.; González-González, V. [Universidad Autónoma de Nuevo León, Facultad de Ingeniería Mecánica y Eléctrica (Mexico)

2016-01-15

In this contribution, we report on the tuning of magnetic properties of cobalt-ferrite nanoclusters. The cobalt-ferrite nanoclusters were synthesized from a two-step approach that consists of the synthesis of cobalt-ferrite nanoparticles in organic media, followed by their dispersion into aqueous dissolution to form an oil-in-water emulsion. These emulsions were prepared at three different concentrations of the cationic surfactant cetyltrimethylammonium bromide (CTAB), in order to control the size and clustering density of the nanoparticles in the nanoclusters. The synthesized samples were characterized by transmission electron microscopy and their related techniques, such as bright-field and Z-contrast imaging, electron diffraction and energy-dispersive X-ray spectrometry; as well as static magnetic measures. The experimental evidence indicates that the size, morphology, and nanoparticles clustering density in the nanoclusters is highly dependent of the cobalt-ferrite:CTAB molar ratio that is used in their synthesis. In addition, due to the clustering of the nanoparticles into the nanoclusters, their magnetic moments are blocked to relax cooperatively. Hence, the magnetic response of the nanoclusters can be tailored by controlling the size and nanoparticles clustering density.

Nanotoxicity of cobalt induced by oxidant generation and glutathione depletion in MCF-7 cells.

Science.gov (United States)

Akhtar, Mohd Javed; Ahamed, Maqusood; Alhadlaq, Hisham A; Alshamsan, Aws

2017-04-01

There are very few studies regarding the biological activity of cobalt-based nanoparticles (NPs) and, therefore, the possible mechanism behind the biological response of cobalt NPs has not been fully explored. The present study was designed to explore the potential mechanisms of the cytotoxicity of cobalt NPs in human breast cancer (MCF-7) cells. The shape and size of cobalt NPs were characterized by scanning and transmission electron microscopy (SEM and TEM). The crystallinity of NPs was determined by X-ray diffraction (XRD). The dissolution of NPs was measured in phosphate-buffered saline (PBS) and culture media by atomic absorption spectroscopy (AAS). Cytotoxicity parameters, such as [3-(4,5-dimethyl thiazol-2-yl)-2,5-diphenyl tetrazolium bromide] (MTT), neutral red uptake (NRU), and lactate dehydrogenase (LDH) release suggested that cobalt NPs were toxic to MCF-7 cells in a dose-dependent manner (50-200μg/ml). Cobalt NPs also significantly induced reactive oxygen species (ROS) generation, lipid peroxidation (LPO), mitochondrial outer membrane potential loss (MOMP), and activity of caspase-3 enzymes in MCF-7 cells. Moreover, cobalt NPs decreased intracellular antioxidant glutathione (GSH) molecules. The exogenous supply of antioxidant N-acetyl cysteine in cobalt NP-treated cells restored the cellular GSH level and prevented cytotoxicity that was also confirmed by microscopy. Similarly, the addition of buthionine-[S, R]-sulfoximine, which interferes with GSH biosynthesis, potentiated cobalt NP-mediated toxicity. Our data suggested that low solubility cobalt NPs could exert toxicity in MCF-7 cells mainly through cobalt NP dissolution to Co 2+ . Copyright © 2016 Elsevier Ltd. All rights reserved.

Adsorption, Bioaccumulation and Kinetics Parameters of the Phytoremediation of Cobalt from Wastewater Using Elodea canadensis.

Science.gov (United States)

Mosoarca, Giannin; Vancea, Cosmin; Popa, Simona; Boran, Sorina

2018-05-01

Present paper investigates the phytoremediation of cobalt from wastewaters using Elodea canadensis. Bioaccumulation tests were conducted at various concentrations of cobalt ranging from 1 to 15 mg/L. Final concentrations of cobalt in wastewaters, after phytoremediation, were less than 1 mg/L. E. canadensis' hyperaccumulator character with regard to cobalt is emphasised by the amount of cobalt retained: 0.39% ± 0.02% of dry mass at an initial concentration in wastewater of 15 mg/L. After 14 days of exposure to contaminant, the biomass as well as the relative growth rate has increased with the amount of cobalt in wastewaters, the plant manifesting an excellent tolerance to cobalt exposure. Adsorption of cobalt ions by E. canadensis can be well described by the Langmuir adsorption isotherm and the pseudo-second-order model equation.

Activation of cobalt 60 in the LVR-15 reactor core

International Nuclear Information System (INIS)

Melichar, F.

1995-12-01

Cobalt disks were irradiated in the LVR-15 reactor and the relevant cobalt-60 production parameters, particularly the formation rate, were measured. The data were compared with those from previous work by other authors and some discrepancies were found. It is concluded that additional experiments have to be performed in order to obtain reliable data, usable in economic balance assessment with respect to the use of hot chambers for the production of sealed cobalt-60 sources. (P.A.). 4 tabs., 3 refs., 10 annexes

Nickel and cobalt release from jewellery and metal clothing items in Korea.

Science.gov (United States)

Cheong, Seung Hyun; Choi, You Won; Choi, Hae Young; Byun, Ji Yeon

2014-01-01

In Korea, the prevalence of nickel allergy has shown a sharply increasing trend. Cobalt contact allergy is often associated with concomitant reactions to nickel, and is more common in Korea than in western countries. The aim of the present study was to investigate the prevalence of items that release nickel and cobalt on the Korean market. A total of 471 items that included 193 branded jewellery, 202 non-branded jewellery and 76 metal clothing items were sampled and studied with a dimethylglyoxime (DMG) test and a cobalt spot test to detect nickel and cobalt release, respectively. Nickel release was detected in 47.8% of the tested items. The positive rates in the DMG test were 12.4% for the branded jewellery, 70.8% for the non-branded jewellery, and 76.3% for the metal clothing items. Cobalt release was found in 6.2% of items. Among the types of jewellery, belts and hair pins showed higher positive rates in both the DMG test and the cobalt spot test. Our study shows that the prevalence of items that release nickel or cobalt among jewellery and metal clothing items is high in Korea. © 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Physical and electrochemical study of cobalt oxide nano- and microparticles

Energy Technology Data Exchange (ETDEWEB)

Alburquenque, D. [Dpto. de Química de los Materiales, USACh, Av. L.B.O.‘Higgins 3363, 9170022 Santiago (Chile); Dpto. de Metalurgia, USACh, Av. Ecuador 3469, 9170124, Santiago (Chile); Vargas, E. [Dpto. de Física, USACh and CEDENNA, Av. Ecuador 3493, 9170124 Santiago (Chile); Dpto. de Metalurgia, USACh, Av. Ecuador 3469, 9170124, Santiago (Chile); Denardin, J.C.; Escrig, J. [Dpto. de Física, USACh and CEDENNA, Av. Ecuador 3493, 9170124 Santiago (Chile); Marco, J.F. [Instituto de Química Física “Rocasolano”, CSIC, c/Serrano 119, 28006 Madrid (Spain); Ortiz, J. [Dpto. de Química de los Materiales, USACh, Av. L.B.O.‘Higgins 3363, 9170022 Santiago (Chile); Gautier, J.L., E-mail: juan.gautier@usach.cl [Dpto. de Química de los Materiales, USACh, Av. L.B.O.‘Higgins 3363, 9170022 Santiago (Chile)

2014-07-01

Cobalt oxide nanocrystals of size 17–21 nm were synthesized by a simple reaction between cobalt acetate (II) and dodecylamine. On the other hand, micrometric Co{sub 3}O{sub 4} was prepared using the ceramic method. The structural examination of these materials was performed using powder X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and transmission electron microscopy (TEM and HRTEM). XRD studies showed that the oxides were pure, well-crystallized, spinel cubic phases with a-cell parameter of 0.8049 nm and 0.8069 nm for the nano and micro-oxide, respectively. The average particle size was 19 nm (nano-oxide) and 1250 μm (micro-oxide). Morphological studies carried out by SEM and TEM analyses have shown the presence of octahedral particles in both cases. Bulk and surface properties investigated by X-ray photoelectron spectroscopy (XPS), point zero charge (pzc), FTIR and cyclic voltammetry indicated that there were no significant differences in the composition on both materials. The magnetic behavior of the samples was determined using a vibrating sample magnetometer. The compounds showed paramagnetic character and no coercivity and remanence in all cases. Galvanostatic measurements of electrodes formed with nanocrystals showed better performance than those built with micrometric particles. - Highlights: • Spinel Co{sub 3}O{sub 4} nanoparticles and microparticles with same structure but with different cell parameters, particle size and surface area were synthesized. • Oxide nanoparticles showed better electrochemical behavior than micrometric ones due to area effect.

World production and possible recovery of cobalt from the Kupferschiefer stratiform copper ore

Directory of Open Access Journals (Sweden)

Pazik Paulina M.

2016-01-01

Full Text Available Cobalt is recognized as a strategic metal and also E-tech element, which is crucial for worlds development. An increasing demand for cobalt forces for searching of new resources that could be explored in European countries. There are many examples of cobalt recoveries, mostly from laterite and sulphide deposits. However, the accurate choice of the technology depends on many factors. The Kupferschiefer stratiform copper ore located in Poland is the biggest deposit of cobalt in Europe. Although KGHM Polska Miedz S.A. recovers many precious metals from this ore, cobalt is not recovered yet. This metal occurs as an accompanying element, mostly in the form of cobaltite (CaAsS, with the average content of 50–80 g/Mg. In this paper a possible recovery of cobalt from the Kupferschiefer ore, with the use of hydrometallurgical methods, was investigated.

Importance of cobalt for individual trophic groups in an anaerobic methanol-degrading consortium.

OpenAIRE

Florencio, L; Field, J A; Lettinga, G

1994-01-01

Methanol is an important anaerobic substrate in industrial wastewater treatment and the natural environment. Previous studies indicate that cobalt greatly stimulates methane formation during anaerobic treatment of methanolic wastewaters. To evaluate the effect of cobalt in a mixed culture, a sludge with low background levels of cobalt was cultivated in an upflow anaerobic sludge blanket reactor. Specific inhibitors in batch assays were then utilized to study the effect of cobalt on the growth...

hermo-Physical and Mechanical Properties of Unsaturated Polyester /Cobalt Ferrite Composites

Directory of Open Access Journals (Sweden)

Lamees Salam Faiq

2017-04-01

Full Text Available Unsaturated polyester was used as a matrix which was filled with different percentages of cobalt ferrite using hand lay-up method. Cobalt ferrite was synthesized using solid state ceramic method with reagent of CoO and Fe2O3. Mechanical properties such tensile strength, Young's modulus and shore D hardness of the composite have been studied. All these properties have increased by 10% with increasing cobalt ferrite contents. Also the thermal properties such thermal conductivity and specific heat capacity are highly increased as the ferrite content increased, while the thermal diffusivity increased by 22 %. On the other hand dielectric strength of composite has been measured which increased by 50% by increasing the cobalt ferrite content.

Contact dermatitis to cobalt chloride with an unusual mechanism.

Science.gov (United States)

Arslan, Sevket; Aksan, Serkan; Ucar, Ramazan; Caliskaner, Ahmet Zafer

2015-10-01

Contact dermatitis is a frequent inflammatory skin disease. A suspected diagnosis is based on clinical symptoms, a plausible contact to allergens and a suitable history of dermatitis. Therefore, careful diagnosis by patch testing is of great importance because the patch testing is important to find out which allergen/material causes the complaints. Metallic allergens such as cobalt are among the most common causes of allergic contact dermatitis, but frequencies of contact dermatitis to these allergens may vary in different skin areas. Here, we report an unusual case of cobalt allergy on the skin contact with the prosthetic leg of a 30-year-old female patient. The patient developed maculopapular and vesicular lesions on her contact region of residual limb to prosthetic leg. She underwent standard patch testing, which resulted in a strong positive reaction to cobalt chloride. This case report may serve to remind doctors to be aware of potential allergic reactions to prostheses and to enable them to recognize a metal allergy if it appears. Prosthetists should also be reminded of potential allergic reactions. Cobalt can be used as an accelerator in making a prosthetic socket. Several cases have been reported concerning allergies to components of the prosthetic socket. This is the first report of sensitization to cobalt which is used in making a prosthetic leg. © The International Society for Prosthetics and Orthotics 2014.

Ligand field effects in the nuclear magnetic shielding of nitrogen-15 and cobalt-59 in bent nitrosyl complexes of cobalt(III)

International Nuclear Information System (INIS)

Duffin, P.A.; Larkworthy, L.F.; Mason, J.; Stephens, A.N.; Thompson, R.M.

1987-01-01

A range of square-pyramidal complexes of cobalt(III) with a bent apical nitrosyl ligand has been prepared and examined by 15 N and 59 Co NMR spectroscopy, in a study of nephelauxetic and spectrochemical effects at the metal and nitrogen nuclei in the bent Co-NO chromophore. The basal ligands in this comparison include dithiocarbamate, quadridentate Schiff base or porphine, and bis-chelating diamine or oximate, so as to give S 4 , S 2 N 2 , N 4 , OONN, or ONON coordination in the plane and a range of substituents in the chelate and phenylene rings. The shielding of both cobalt and nitrogen tends to decrease with decrease in the M(d) → π*(NO) back-bonding, as indicated by the MN and NO bond distances, the MNO angle and the NO stretching frequency. The shieldings decrease from sulfur to nitrogen to oxygen coligators and also with electron withdrawal by ring substituents (and vice versa), i.e. with decrease in the ligand field splitting and in the nephelauxetism of the coligands. These parallelisms of the cobalt and nitrogen shielding accord with the orbital theory that was developed to explain the bending of the MNO ligand and influences of the metal and coligands. Significant interdependence of spectrochemical and nephelauxetic effects at cobalt and nitrogen arises from the degree of overlap and similarity in energies of the frontier orbitals for the paramagnetic circulation at nitrogen [n(N) → π* (NO)] and at cobalt (d-d). 43 references, 5 figures, 2 tables

Construction of an apparatus for nuclear orientation measurements at low temperatures. Application to neodymium-cobalt alloy

International Nuclear Information System (INIS)

Mayer, E.

1965-10-01

We describe experiments along which has been studied the anisotropy of γ radiations emitted by oriented nuclei. We have used the great hyperfine fields acting on nuclei in ferromagnetic metals so as to produce alignment at low temperature. By irradiation we obtained a few cobalt 60 nuclei in our samples which were then cooled down to 0,01 K. The anisotropic rate of the 1,33 MeV γ radiation was measured in function of the sample temperature, using as thermometer the anisotropy of γ radiation emitted by cobalt 60 nuclei in a cobalt single crystal. Cobalt 60 was lined up in a cobalt nickel alloy (40% Ni). The hyperfine field at the cobalt was measured compared to the effective field in metallic cobalt: Heff(Co Ni)/Heff(Co metal) = 0.71 ± 0.12. These results are in good agreement with specific heat measurements made previously. Cobalt 60 has been polarised in a neodymium-cobalt alloy (NdCo 5 ). The field at the cobalt in NdCo 5 has been measured compared to the field in metallic cobalt and taking the non-saturation into account we found 165000 oersteds 5 ) [fr

21 CFR 189.120 - Cobaltous salts and its derivatives.

Science.gov (United States)

2010-04-01

... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Cobaltous salts and its derivatives. 189.120 Section 189.120 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES... malt beverages as a foam stabilizer and to prevent “gushing.” (b) Food containing any added cobaltous...

Study of the point defects formed in cobalt by electron bombardment; Etude des defauts ponctuels crees par bombardement electronique dans le cobalt

Energy Technology Data Exchange (ETDEWEB)

Sulpice, G [Commissariat a l' Energie Atomique, 38 - Grenoble (France). Centre d' Etudes Nucleaires

1968-12-01

A study of the point defects formed in cobalt by electron bombardment is presented. The results are compared with those previously obtained for two other ferromagnetic metals of different structure, iron and nickel. In the first part we give a review of the literature concerning the creation of point defects, their contribution to resistivity and their annihilation mode in the three structure types. We then describe the experimental techniques adapted, in particular the study of the resistivity increase during a linear temperature rise. Our investigations concern the following, essential points : the observation of the successive annihilation stages of the point defects formed in pure cobalt, a study of the variations with respect to the doses and energy of the incident particles, and the determination of the annealing kinetics and the corresponding activation energies. The results are finally compared with the various models of point defect annihilation proposed for other metals: none of these interpretations is in perfect agreement with our results. In the case of cobalt we are thus led to modify the model proposed by our laboratory for iron an nickel. The difference between these three metals is explained by the anisotropic character of the cobalt matrix. (author) [French] Nous presentons une etude des defauts ponctuels crees par bombardement electronique dans le cobalt et comparons nos resultats a ceux obtenus precedemment dans deux autres metaux ferromagnetiques de structure differente, le fer et le nickel. Dans une premiere partie nous faisons une mise au point bibliographique comparee sur la creation des defauts, leur contribution a la resistivite et leur mode d'annihilation dans les trois types de structure. Nous decrivons ensuite les techniques experimentales mises au point, en particulier l'etude du revenu de la resistivite au cours d'une montee lineaire de temperature. Au cours de ce travail, nous avons mis en evidence les stades successifs d

Cobalt(I) and Cobalt(III) Cyclopentadienyl Complexes with New Silicon-branched Fluorous Tags

Czech Academy of Sciences Publication Activity Database

Strašák, Tomáš; Čermák, Jan; Červenková Šťastná, Lucie; Sýkora, Jan; Fajgar, Radek

2014-01-01

Roč. 159, MAR 2014 (2014), s. 15-20 ISSN 0022-1139 R&D Projects: GA ČR(CZ) GAP106/12/1372 Institutional support: RVO:67985858 Keywords : fluorous tag * cobalt complex * cyclopentadienyl complex Subject RIV: CC - Organic Chemistry Impact factor: 1.948, year: 2014

Effects of cobalt on structure, microchemistry and properties of a wrought nickel-base superalloy

Science.gov (United States)

Jarrett, R. N.; Tien, J. K.

1982-01-01

The effect of cobalt on the basic mechanical properties and microstructure of wrought nickel-base superalloys has been investigated experimentally by systematically replacing cobalt by nickel in Udimet 700 (17 wt% Co) commonly used in gas turbine (jet engine) applications. It is shown that the room temperature tensile yield strength and tensile strength only slightly decrease in fine-grained (disk) alloys and are basically unaffected in coarse-grained (blading) alloys as cobalt is removed. Creep and stress rupture resistances at 760 C are found to be unaffected by cobalt level in the blading alloys and decrease sharply only when the cobalt level is reduced below 8 vol% in the disk alloys. The effect of cobalt is explained in terms of gamma prime strengthening kinetics.

Cobalt oxide nanoparticles as a novel high-efficiency fiber coating for solid phase microextraction of benzene, toluene, ethylbenzene and xylene from aqueous solutions

International Nuclear Information System (INIS)

Gholivand, Mohammad Bagher; Shamsipur, Mojtaba; Shamizadeh, Mohammad; Moradian, Rostam; Astinchap, Bandar

2014-01-01

Highlights: • Co 3 O 4 nanoparticles were introduced as a novel SPME fiber coating. • The fiber was evaluated for the extraction of BTEX in combination with GC–MS. • The fiber showed extraction efficiencies better than a PDMS fiber toward BTEX. • The fiber was successfully applied to the determination of BTEX in real samples. - Abstract: In this work cobalt oxide nanoparticles were introduced for preparation of a novel solid phase microextraction (SPME) fiber coating. Chemical bath deposition (CBD) technique was used in order for synthesis and immobilization of the Co 3 O 4 nanomaterials on a Pt wire for fabrication of SPME fiber. The prepared cobalt oxide coating was characterized by scanning electron microscopy (SEM) and X-ray diffraction (XRD) analysis. The fiber was evaluated for the extraction of benzene, toluene, ethylbenzene and xylene (BTEX) in combination with GC–MS. A simplex optimization method was used to optimize the factors affecting the extraction efficiency. Under optimized conditions, the proposed fiber showed extraction efficiencies comparable to those of a commercial polydimethylsiloxane (PDMS) fiber toward the BTEX compounds. The repeatability of the fiber and its reproducibility, expressed as relative standard deviation (RSD), were lower than about 11%. No significant change was observed in the extraction efficiency of the new SPME fiber after over 50 extractions. The fiber was successfully applied to the determination of BTEX compounds in real samples. The proposed nanostructure cobalt oxide fiber is a promising alternative to the commercial fibers as it is robust, inexpensive and easily prepared

Cobalt oxide nanoparticles as a novel high-efficiency fiber coating for solid phase microextraction of benzene, toluene, ethylbenzene and xylene from aqueous solutions

Energy Technology Data Exchange (ETDEWEB)

Gholivand, Mohammad Bagher, E-mail: MB.Gholivand@yahoo.com [Department of Analytical Chemistry, Faculty of Chemistry, Razi University, Kermanshah (Iran, Islamic Republic of); Shamsipur, Mojtaba; Shamizadeh, Mohammad [Department of Analytical Chemistry, Faculty of Chemistry, Razi University, Kermanshah (Iran, Islamic Republic of); Moradian, Rostam; Astinchap, Bandar [Physics Department, Faculty of Science, Razi University, Kermanshah (Iran, Islamic Republic of); Nano Technology Research Laboratory, Razi University, Kermanshah (Iran, Islamic Republic of)

2014-04-01

Highlights: • Co{sub 3}O{sub 4} nanoparticles were introduced as a novel SPME fiber coating. • The fiber was evaluated for the extraction of BTEX in combination with GC–MS. • The fiber showed extraction efficiencies better than a PDMS fiber toward BTEX. • The fiber was successfully applied to the determination of BTEX in real samples. - Abstract: In this work cobalt oxide nanoparticles were introduced for preparation of a novel solid phase microextraction (SPME) fiber coating. Chemical bath deposition (CBD) technique was used in order for synthesis and immobilization of the Co{sub 3}O{sub 4} nanomaterials on a Pt wire for fabrication of SPME fiber. The prepared cobalt oxide coating was characterized by scanning electron microscopy (SEM) and X-ray diffraction (XRD) analysis. The fiber was evaluated for the extraction of benzene, toluene, ethylbenzene and xylene (BTEX) in combination with GC–MS. A simplex optimization method was used to optimize the factors affecting the extraction efficiency. Under optimized conditions, the proposed fiber showed extraction efficiencies comparable to those of a commercial polydimethylsiloxane (PDMS) fiber toward the BTEX compounds. The repeatability of the fiber and its reproducibility, expressed as relative standard deviation (RSD), were lower than about 11%. No significant change was observed in the extraction efficiency of the new SPME fiber after over 50 extractions. The fiber was successfully applied to the determination of BTEX compounds in real samples. The proposed nanostructure cobalt oxide fiber is a promising alternative to the commercial fibers as it is robust, inexpensive and easily prepared.

Enhanced activity of gold-supported cobalt oxide for the electrochemical evolution of oxygen.

Science.gov (United States)

Yeo, Boon Siang; Bell, Alexis T

2011-04-13

Scanning electron microscopy, linear sweep voltammetry, chronoamperometry, and in situ surface-enhanced Raman spectroscopy were used to investigate the electrochemical oxygen evolution reaction (OER) occurring on cobalt oxide films deposited on Au and other metal substrates. All experiments were carried out in 0.1 M KOH. A remarkable finding is that the turnover frequency for the OER exhibited by ∼0.4 ML of cobalt oxide deposited on Au is 40 times higher than that of bulk cobalt oxide. The activity of small amounts of cobalt oxide deposited on Pt, Pd, Cu, and Co decreased monotonically in the order Au > Pt > Pd > Cu > Co, paralleling the decreasing electronegativity of the substrate metal. Another notable finding is that the OER turnover frequency for ∼0.4 ML of cobalt oxide deposited on Au is nearly three times higher than that for bulk Ir. Raman spectroscopy revealed that the as-deposited cobalt oxide is present as Co(3)O(4) but undergoes progressive oxidation to CoO(OH) with increasing anodic potential. The higher OER activity of cobalt oxide deposited on Au is attributed to an increase in fraction of the Co sites present as Co(IV) cations, a state of cobalt believed to be essential for OER to occur. A hypothesis for how Co(IV) cations contribute to OER is proposed and discussed. © 2011 American Chemical Society

Speciation analysis of cobalt in foods by high-performance liquid chromatography and neutron activation analysis

International Nuclear Information System (INIS)

Muto, Toshio; Koyama, Motoko

1994-01-01

A combined method by coupling high-performance liquid chromatography (HPLC, as a separation method) with neutron activation analysis (as a detection method) have been applied to the speciation analysis of cobalt in daily foods (e.g. egg, fish and milk). Cobalt species including free cobalt, vitamin B 12 and protein-bound cobalt were separated with a preparative HPLC and a centrifuge. Subsequently, the determination of cobalt in the separated species was made by neutron activation analysis. The results showed that the content of the total cobalt in the foods was found to lie in the range 0.4-11ng/g(0.4-11ppb) based on wet weight. The compositions of free cobalt, vitamin B 12 and protein-bound cobalt were ranged 16-43%, 55-73%, 2.3-17%, respectively. These experimental evidences suggest that the combination of HPLC and neutron activation analysis is expected to be a useful tool for speciation analysis of trace elements in biological as well as environmental materials. (author)

Brightness coatings of zinc-cobalt alloys by electrolytic way

International Nuclear Information System (INIS)

Julve, E.

1993-01-01

Zinc-cobalt alloys provide corrosion resistance for the ferrous based metals. An acidic electrolyte for zinc-cobalt electrodeposition is examined in the present work. The effects of variations in electrolyte composition, in electrolyte temperature, pH and agitation on electrodeposit composition have been studied, as well as the current density influence. It was found that the following electrolyte gave the optimum results: 79 g.1''-1 ZnCl 2 , 15.3 g.1''-1 CoCl 2 .6H 2 O, 160 g.1''-1 KCl, 25 g.1''-1 H 3 BO 3 and 5-10 cm''3.1''-1 of an organic additive (caffeine, coumarin and sodium lauryl-sulphonate). The operating conditions were: pH=5,6 temperature: 30 degree centigree, current density: 0,025-0,035 A. cm''2, anode: pure zinc, agitation: slowly with air and filtration: continuous. The throwing power and cathode current efficiency of the electrolyte were also studied. This electrolyte yielded zinc-cobalt alloys white and lustrous and had a cobalt content of 0,5-0,8% (Author) 3 refs. 5 fig

Hepatic lipidosis associated with cobalt deficiency in Omani goats.

Science.gov (United States)

Johnson, E H; Muirhead, D E; Annamalai, K; King, G J; Al-Busaidy, R; Hameed, M S

1999-06-01

Livers from 36 of 684 (5.3%) apparently healthy goats examined at an abattoir in the greater Muscat area of Oman exhibited gross pathological findings characterized by extremely pale, friable, fatty livers encompassing the entire organ. Histopathologically, diffuse hepatic lipidosis and occasional bile duct proliferation were observed. Periodic acid Schiff-positive, diastase-resistant pigment was observed in the macrophages lining the sinusoids. These histopathological lesions were consistent with those characteristic of ovine white liver disease. Cobalt analysis revealed that normal livers had six times more cobalt and a 3-fold less fat content than those measured in the fatty livers. This is the first report of an association between cobalt deficiency and hepatic lipidosis in Omani goats.

Manganese substituted cobalt ferrite magnetostrictive materials for magnetic stress sensor applications

OpenAIRE

Paulsen, J. A.; Ring, A. P.; Lo, C. C. H.; Snyder, John Evan; Jiles, David

2005-01-01

Metal bonded cobalt ferrite composites have been shown to be promising candidate materials for use in magnetoelastic stress sensors, due to their large magnetostriction and high sensitivity of magnetization to stress. However previous results have shown that below 60 °C the cobalt ferrite material exhibits substantial magnetomechanical hysteresis. In the current study, measurements indicate that substituting Mn for some of the Fe in the cobalt ferrite can lower the Curie temperature of the ma...

Cobalt coatings: deposition on a nickel substrate and electrocatalytic activity for alkaline water electrolysis

Energy Technology Data Exchange (ETDEWEB)

Brossard, L. (Inst. de Recherche d' Hydro-Quebec (IREQ), Varennes, Quebec (Canada))

1992-02-01

The deposition of cobalt on a nickel substrate in 30 wt% KOH aqueous solution containing dissolved cobalt was investigated. The effect of the applied cathodic current density (i{sub a}) and the dissolved-cobalt concentration in the electrolyte on the deposition rate suggests that the rate-determining step is the diffusion of the dissolved cobalt in the solution. The faradic efficiency of the cobalt deposition reaction and the coating morphology are linked to i{sub a}, while the evolution rate of both oxygen and hydrogen in 30 wt% KOH at 70degC is dependent on the coating morphology. (orig.).

Adsorption Study of Cobalt on Treated Granular Activated Carbon

OpenAIRE

Y. V. Hete; S. B. Gholase; R. U. Khope

2012-01-01

This study is carried out for the removal of cobalt from aqueous solution using granular activated carbon in combination with p-nitro benzoic acid at temperature 25±1 °C. The adsorption isotherm of cobalt on granular activated carbon has been determined and the data fitted reasonably well to the Langmuir and Freundlich isotherm for activated carbon.

Microwave Mapping Demonstration Using the Thermochromic Cobalt Chloride Equilibrium

Science.gov (United States)

Nguyen, Vu D.; Birdwhistell, Kurt R.

2014-01-01

An update to the thermochromic cobalt(II) chloride equilibrium demonstration is described. Filter paper that has been saturated with aqueous cobalt(II) chloride is heated for seconds in a microwave oven, producing a color change. The resulting pink and blue map is used to colorfully demonstrate Le Châtelier's principle and to illuminate the…

Tribological research of cobalt alloys used as biomaterials

Directory of Open Access Journals (Sweden)

Robert Karpiński

2015-12-01

Full Text Available This study provides information about the cobalt alloys used in dentistry and medicine. The work includes a review of the literature describing the general properties of cobalt alloys. In addition it describes the impact of the manufacturing conditions and alloy additives used , on the structure and mechanical properties of these alloys. The research methodology and the results obtained has been presented in the study. Two cobalt-based alloys Co-CrMo-W and Co-Cr-Ni-Mo were selected for the tests. The first one was prepared with the use of casting technique whereas the second was obtained due to plastic forming. An analysis of the chemical composition and in vitro tribological tests with the use of tribotester of "ball-on-disc" type was conducted. Comparative tribological characteristics of these alloys has been presented.

Plasma Deposition and Characterization of Copper-doped Cobalt Oxide Nanocatalysts

Directory of Open Access Journals (Sweden)

Jacek TYCZKOWSKI

2013-09-01

Full Text Available A series of pure and copper-doped cobalt oxide films was prepared by plasma-enhanced metalorganic chemical vapor deposition (PEMOCVD. The effect of Cu-doping on the chemical structure and morphology of the deposited films was investigated. Raman and FTIR spectroscopies were used to characterize the chemical structure and morphology of the produced films. The bulk composition and homogeneity of the samples were investigated by energy dispersive X-ray microanalysis (EDX, and X-ray photoelectron spectroscopy (XPS was employed to assess the surface chemical composition of pure and doped materials. The obtained results permit to affirm that the PEMOCVD technique is a simple, versatile and efficient method for providing homogeneous layers of cobalt oxides with a different content of copper. It has been found that pure cobalt oxide films mainly contain Co3O4 in the form of nanoclusters whereas the films doped with Cu are much more complex, and CoOx (also Co3O4, mixed Co-Cu oxides and CuOx nanoclusters are detected in them. Preliminary catalytical tests show that Cu-doped cobalt oxide films allow to initiate catalytic combustion of n-hexane at a lower temperature compared to the pure cobalt oxide (Co3O4 films. From what has been stated above, the plasma-deposited thin films of Cu-doped cobalt oxides pave the way towards a new class of nanomaterials with interesting catalytic properties. DOI: http://dx.doi.org/10.5755/j01.ms.19.3.2320

Fischer-Tropsch Cobalt Catalyst Activation and Handling Through Wax Enclosure Methods

Science.gov (United States)

Klettlinger, Jennifer L. S.; Yen, Chia H.; Nakley, Leah M.; Surgenor, Angela D.

2016-01-01

Fischer-Tropsch (F-T) synthesis is considered a gas to liquid process which converts syn-gas, a gaseous mixture of hydrogen and carbon monoxide, into liquids of various hydrocarbon chain length and product distributions. Cobalt based catalysts are used in F-T synthesis and are the focus of this paper. One key concern with handling cobalt based catalysts is that the active form of catalyst is in a reduced state, metallic cobalt, which oxidizes readily in air. In laboratory experiments, the precursor cobalt oxide catalyst is activated in a fixed bed at 350 ?C then transferred into a continuous stirred tank reactor (CSTR) with inert gas. NASA has developed a process which involves the enclosure of active cobalt catalyst in a wax mold to prevent oxidation during storage and handling. This improved method allows for precise catalyst loading and delivery into a CSTR. Preliminary results indicate similar activity levels in the F-T reaction in comparison to the direct injection method. The work in this paper was supported by the NASA Fundamental Aeronautics Subsonics Fixed Wing Project.

Bibliographies on radiation chemistry. 9. Metal ions and complexes. Part A: Cobalt, rhodium, iridium

Energy Technology Data Exchange (ETDEWEB)

Hoffman, M Z; Ross, A B

1986-01-01

The one-electron oxidation and reduction of metal ions and complexes can yield species in unusual oxidation states, and ligand-radicals coordinated to the central metal. These often unstable species can be mechanistically important intermediates in thermal, photochemical, and electrochemical reactions involving metal-containing substances. Their generation via radiolysis provides an alternate means of characterizing them using kinetic and spectroscopic techniques. We hope these bibliographies on the radiation chemistry of metal ions and complexes, presented according to periodic groups, will prove useful to researchers in metallo-redox chemistry. These bibliographies contain only primary literature sources; reviews are not included. However, a list of general review articles on the radiation chemistry of metal ions and complexes is presented here in the first section which covers cobalt, rhodium and iridium, Group 9 in the new IUPAC notation. Additional parts of the bibliography are planned, covering other periodic groups. Part A of the bibliography was prepared by a search of the Radiation Chemistry Data Center Bibliographic Data Base (RCDCbib) through January 1986 for papers on rhodium, iridium and cobalt compounds, and radiolysis (both continuous and pulsed). Papers in which the use of metal compounds was incidental to the primary objective of the study were excluded. Excluded also were publications in unrefereed and obscure sources such as meeting proceedings, internal reports, dissertations, and patents. The majority of the studies in the resultant compilation deal with experiments performed on solutions, mainly aqueous, although a substantial fraction is devoted to solid-state esr measurements. The references are listed in separate sections for each of the metals, and are presented in approximate chronological order.

Cobalt doped proangiogenic hydroxyapatite for bone tissue engineering application

International Nuclear Information System (INIS)

Kulanthaivel, Senthilguru; Roy, Bibhas; Agarwal, Tarun; Giri, Supratim; Pramanik, Krishna; Pal, Kunal; Ray, Sirsendu S.; Maiti, Tapas K.; Banerjee, Indranil

2016-01-01

ABSTRACT: The present study delineates the synthesis and characterization of cobalt doped proangiogenic–osteogenic hydroxyapatite. Hydroxyapatite samples, doped with varying concentrations of bivalent cobalt (Co"2"+) were prepared by the ammoniacal precipitation method and the extent of doping was measured by ICP–OES. The crystalline structure of the doped hydroxyapatite samples was confirmed by XRD and FTIR studies. Analysis pertaining to the effect of doped hydroxyapatite on cell cycle progression and proliferation of MG-63 cells revealed that the doping of cobalt supported the cell viability and proliferation up to a threshold limit. Furthermore, such level of doping also induced differentiation of the bone cells, which was evident from the higher expression of differentiation markers (Runx2 and Osterix) and better nodule formation (SEM study). Western blot analysis in conjugation with ELISA study confirmed that the doped HAp samples significantly increased the expression of HIF-1α and VEGF in MG-63 cells. The analysis described here confirms the proangiogenic–osteogenic properties of the cobalt doped hydroxyapatite and indicates its potential application in bone tissue engineering. - Highlights: • Cobalt (Co"+"2) doped hydroxyapatite (Co-HAp) can be prepared by the wet chemical method. • The concentration of Co"+"2 influences the physico-chemical properties of HAp. • Co-HAp was found to be biocompatible and osteogenic. • Co-HAp enhanced cellular VEGF secretion through HIF-1α stabilization. • The optimum biological performance of Co-HAp was achieved for 0.33% (w/w) Co"+"2 doping.

Relationship between nickel and cobalt sensitization in hard metal workers

Energy Technology Data Exchange (ETDEWEB)

Rystedt, I; Fischer, T

1983-05-01

Eight hundred fifty-three hard metal workers were examined and patch tested with 20 substances from their environment, including nickel and cobalt. Nickel sensitivity was found in 2 men and 38 women. 88% of the nickel-sensitive individuals had developed a jewelry dermatitis prior to employment in the hard metal industry or before the appearance of hand eczema. 29% of the hard metal workers gave a history of slight irritant dermatitis. In the nickel sensitized group, 40% had had severe hand eczema which generally appeared 6-12 months after starting employment. In 25% of the cases, nickel sensitive individuals developed cobalt allergy, compared with 5% in the total population investigated. Most facts indicate that nickel sensitivity and irritant hand eczema precede cobalt sensitization. Hard metal workers with simultaneous nickel and cobalt sensitivity had a more severe hand eczema than those with isolated cobalt or nickel sensitivity or only irritant dermatitis. 64% of the female population had pierced ear lobes. Among the nickel allergic women, 95% had pierced ear lobes. The use of earrings containing nickel after piercing is strongly suspected of being the major cause of nickel sensitivity. Piercing at an early age seems to increase the risk of incurring nickel sensitivity.

Chemical bonding and magnetic properties of gadolinium (Gd) substituted cobalt ferrite

Energy Technology Data Exchange (ETDEWEB)

Puli, Venkata Sreenivas, E-mail: vspuli@utep.edu [Department of Mechanical Engineering, University of Texas, El Paso, TX 79968 (United States); Adireddy, Shiva [Department of Physics and Engineering Physics, Tulane University, New Orleans, LA 70118 (United States); Ramana, C.V. [Department of Mechanical Engineering, University of Texas, El Paso, TX 79968 (United States)

2015-09-25

Graphical abstract: Room temperature Raman spectra of CoFe{sub 2−x}Gd{sub x}O{sub 4} (CFGO, x = 0.0–0.3) compounds as a function of wavenumber (cm{sup −1}). - Highlights: • Gd substituted ferrites were synthesized under controlled concentration. • Gd ion induced lattice dynamical changes are significant. • Enhanced magnetization is observed upon Gd-incorporation in cobalt ferrite. • A correlation between lattice dynamics and magnetic properties is established. - Abstract: Polycrystalline gadolinium (Gd) substituted cobalt ferrites (CoFe{sub 2−x}Gd{sub x}O{sub 4}; x = 0–0.3, referred to CFGO) ceramics have been synthesized by solid state reaction method. Chemical bonding, crystal structure and magnetic properties of CFGO compounds have been evaluated as a function of Gd-content. X-ray diffraction (XRD) and Raman spectroscopic analyses confirmed the formation of inverse spinel cubic structure. However, a secondary ortho-ferrite phase (GdFeO{sub 3}) nucleates for higher values of Gd-content. A considerable increase in the saturation magnetization has been observed upon the initial substitution of Gd (x = 0.1). The saturation magnetization drastically decreases at higher Gd content (x ⩾ 0.3). No contribution from ortho-ferrite GdFeO{sub 3} phase is noted to the magnetic properties. The increase in the magnetic saturation magnetization is attributed to the higher magnetic moment of Gd{sup 3+} (4f{sup 7}) residing in octahedral sites is higher when compared to that of Fe{sup 3+} (3d{sup 5}) and as well due to the migration of Co{sup 2+} (3d{sup 7}) ions from the octahedral to the tetrahedral sites with a magnetic moment aligned anti-parallel to those of rare earth (RE{sup 3+}) ions in the spinel lattice. Increase in coercivity with increase in Gd{sup 3+} is content is attributed to magnetic anisotropy in the ceramics.

Leaching kinetics of cobalt from the scraps of spent aerospace magnetic materials.

Science.gov (United States)

Zhou, Xuejiao; Chen, Yongli; Yin, Jianguo; Xia, Wentang; Yuan, Xiaoli; Xiang, Xiaoyan

2018-06-01

Based on physicochemical properties of the scraps of spent aerospace magnetic materials, a roasting - magnetic separation followed by sulfuric acid leaching process was proposed to extract cobalt. Roasting was performed at 500 °C to remove organic impurity. Non-magnetic impurities were reduced by magnetic separation and then the raw material was sieved into desired particle sizes. Acid leaching was carried out to extract cobalt from the scraps and experimental parameters included agitation speed, particle size, initial concentration of sulfuric acid and temperature. Agitation speed higher than 300 r/min had a relatively small impact on the cobalt extraction. As the particle size reduced, the content of cobalt in the raw material decreases and the extraction of cobalt by acid leaching increased at first and decreased afterwards. Raising the initial concentration of sulfuric acid and temperature contributed to improve the cobalt extraction and the influence of temperature was more remarkable. SEM image revealed that the spent aerospace magnetic materials mainly existed in the sliced strip flake with a loose surface and porous structure. Under the experimental condition, the leaching rate of cobalt from the scraps in sulfuric acid solution could be expressed as ln(-ln(1 - α)) = lnk + nlnt. The apparent activation energy was found to be 38.33 kJ/mol and it was mainly controlled by the surface chemical reaction. Copyright © 2018 Elsevier Ltd. All rights reserved.

The role of cobalt ferrite magnetic nanoparticles in medical science

International Nuclear Information System (INIS)

Amiri, S.; Shokrollahi, H.

2013-01-01

The nanotechnology industry is rapidly growing and promises that the substantial changes that will have significant economic and scientific impacts be applicable to a wide range of areas, such as aerospace engineering, nano-electronics, environmental remediation and medical healthcare. In this area, cobalt ferrite nanoparticles have been regarded as one of the competitive candidates because of their suitable physical, chemical and magnetic properties like the high anisotropy constant, high coercivity and high Curie temperature, moderate saturation magnetization and ease of synthesis. This paper introduces the magnetic properties, synthesis methods and some medical applications, including the hyperthermia, magnetic resonance imaging (MRI), magnetic separation and drug delivery of cobalt ferrite nanoparticles. Highlights: ► Cobalt ferrite nanoparticles are one of the most important materials for nanomedicine. ► They have high coercivity and moderate saturation magnetization. ► Cobalt ferrite nanoparticles are synthesized easily. ► They are a good candidate for hyperthermia and magnetic resonance imaging.

The role of cobalt ferrite magnetic nanoparticles in medical science

Energy Technology Data Exchange (ETDEWEB)

Amiri, S.; Shokrollahi, H., E-mail: Shokrollahi@sutech.ac.ir

2013-01-01

The nanotechnology industry is rapidly growing and promises that the substantial changes that will have significant economic and scientific impacts be applicable to a wide range of areas, such as aerospace engineering, nano-electronics, environmental remediation and medical healthcare. In this area, cobalt ferrite nanoparticles have been regarded as one of the competitive candidates because of their suitable physical, chemical and magnetic properties like the high anisotropy constant, high coercivity and high Curie temperature, moderate saturation magnetization and ease of synthesis. This paper introduces the magnetic properties, synthesis methods and some medical applications, including the hyperthermia, magnetic resonance imaging (MRI), magnetic separation and drug delivery of cobalt ferrite nanoparticles. Highlights: Black-Right-Pointing-Pointer Cobalt ferrite nanoparticles are one of the most important materials for nanomedicine. Black-Right-Pointing-Pointer They have high coercivity and moderate saturation magnetization. Black-Right-Pointing-Pointer Cobalt ferrite nanoparticles are synthesized easily. Black-Right-Pointing-Pointer They are a good candidate for hyperthermia and magnetic resonance imaging.

Valence control of cobalt oxide thin films by annealing atmosphere

International Nuclear Information System (INIS)

Wang Shijing; Zhang Boping; Zhao Cuihua; Li Songjie; Zhang Meixia; Yan Liping

2011-01-01

The cobalt oxide (CoO and Co 3 O 4 ) thin films were successfully prepared using a spin-coating technique by a chemical solution method with CH 3 OCH 2 CH 2 OH and Co(NO 3 ) 2 .6H 2 O as starting materials. The grayish cobalt oxide films had uniform crystalline grains with less than 50 nm in diameter. The phase structure is able to tailor by controlling the annealing atmosphere and temperature, in which Co 3 O 4 thin film was obtained by annealing in air at 300-600, and N 2 at 300, and transferred to CoO thin film by raising annealing temperature in N 2 . The fitted X-ray photoelectron spectroscopy (XPS) spectra of the Co2p electrons are distinguishable from different valence states of cobalt oxide especially for their satellite structure. The valence control of cobalt oxide thin films by annealing atmosphere contributes to the tailored optical absorption property.

Titanium oxide modification with oxides of mixed cobalt valence for photo catalysis

Energy Technology Data Exchange (ETDEWEB)

Alanis O, R.; Jimenez B, J., E-mail: jaime.jimenez@inin.gob.m [ININ, Departamento de Quimica, Carretera Mexico-Toluca s/n, 52750 Ocoyoacac, Estado de Mexico (Mexico)

2010-07-01

In the present work, heterogenous photo catalysis, a technique often used for organic compound degradation toxic in water, was used. The photo catalyst most often used in this technique is TiO{sub 2}, which due to its physical and chemical properties, can degrade a great number of organic compounds. In addition, in recent years it has been verified that the doping of semiconductors with metals or metallic oxides increases the photo catalytic activity of these semiconductors, which is why it was proposed for doping by the impregnating method using commercial TiO{sub 2} synthesized by the Degussa company (TiO{sub 2} Degussa P25) with and oxide of mixed cobalt valence (Co{sub 3}O{sub 4}) synthesized using the sol-gel method. The synthesized photo catalyst TiO{sub 2}/Co{sub 3}O{sub 4} was characterized by the techniques of X-ray diffraction, scanning electronic microscopy, Raman spectroscopy and finally, photo catalytic tests by means of the degradation of methylene blue. (Author)

Antibacterial activity of cobalt(II complexes with some benzimidazole derivatives

Directory of Open Access Journals (Sweden)

S. O. PODUNAVAC-KUZMANOVIC

2008-12-01

Full Text Available The antibacterial activities of cobalt(II complexes with two series of benzimidazoles were evaluated in vitro against three Gram-positive bacterial strains (Bacillus cereus, Staphylococcus aureus, and Sarcina lutea and one Gram-negative isolate (Pseudomonas aeruginosa. The minimum inhibitory concentration was determined for all the complexes. The majority of the investtigated complexes displayed in vitro inhibitory activity against very persistent bacteria. They were found to be more active against Gram-positive than Gram-negative bacteria. It may be concluded that the antibacterial activity of the compounds is related to the cell wall structure of the tested bacteria. Comparing the inhibitory activities of the tested complexes, it was found that the 1-substituted-2-aminobenzimidazole derivatives were more active than complexes of 1-substituted-2-amino-5,6-dimethylbenzimidazoles. The effect of chemical structure on the antibacterial activity is discussed.

Adsorption Study of Cobalt on Treated Granular Activated Carbon

Directory of Open Access Journals (Sweden)

Y. V. Hete

2012-01-01

Full Text Available This study is carried out for the removal of cobalt from aqueous solution using granular activated carbon in combination with p-nitro benzoic acid at temperature 25±1 °C. The adsorption isotherm of cobalt on granular activated carbon has been determined and the data fitted reasonably well to the Langmuir and Freundlich isotherm for activated carbon.

X-Ray K Absorption Edge Structures of Ligand Chlorine Ion in Some Cobalt Coordination Compounds

Science.gov (United States)

Obashi, Masayoshi; Matsukawa, Tokuo

1983-03-01

The X-ray Cl K absorption spectra in [Co(NH3)6]Cl3, [Co(NH3)5Cl]Cl2, trans-[Co(NH3)4Cl2]Cl and Cs2[CoCl4] are measured with a high-resolution vacuum two-crystal spectrometer. The spectra, except that of [Co(NH3)6]Cl3, show an extremely narrow absorption line at the absorption threshold. The result is interpreted on the basis of molecular orbital theory and it is proposed that the intensity of these narrow absorption lines depends on the chemical state between the cobalt and ligand chlorine ions. The narrow absorption line may well be attributed to transitions of the Cl 1s electron into the eg* antibonding orbitals having partially the 3p character of chlorine in [Co(NH3)5Cl]Cl2 and trans-[Co(NH3)4Cl2]Cl. In Cs2[CoCl4] it may be ascribed to the Cl 1s-t2* transitions.

C-188 cobalt-60 sealed source integrity: source monitoring

International Nuclear Information System (INIS)

Defalco, G.M.; Shah, V.

1995-01-01

The integrity of C-188 cobalt-60 sealed sources used for radiation processing will be a key factor in the continued industrial acceptance and growth of gamma irradiation technology. Given the public's relatively poor understanding of most nuclear topics and the news media's tendency to sensationalize events, it is appropriate for suppliers and users of gamma technology to be vigilant and conservative regarding the application of cobalt-60 sources to industrial purposes. Nordion's recent decision to extend the optional warranty on its C-188 cobalt-60 sealed source from 15 years to 20 years is based on over 30 years of data generated from its on-going SOURCE SURVEILLANCE PROGRAM. This paper presents an overview of the C-188 SOURCE SURVEILLANCE PROGRAM. (author)

New avenues in cobalt-60 production at Ontario Hydro

International Nuclear Information System (INIS)

Mylvaganam, C.K.; Ronchka, R.A.

1990-01-01

Ontario Hydro produces cobalt-60 in the control rods of twelve power reactors. These reactors have a typical flux of 2 x 10 14 neutrons/cm 2 /s, making them efficient producers of cobalt-60. Current annual production is 45 million curies. Since the primary function of these reactors is the production of electricity, their flexibility to meet the needs of commercial cobalt production by the control rod route is limited. Ontario Hydro is therefore developing innovative production techniques, making use of the CANDU reactor's unique ability to be fuelled on-power. These techniques will enable production to better respond to the market's requirements for quantity and specific activity. As it is supplementary to control rod production, annual supply could potentially reach 165 million curies. (author)

Cobalt 60 gamma irradiation current status, trends and insights

International Nuclear Information System (INIS)

Corley, John T.

1998-01-01

This paper discusses the current status, trends and insights into the continued, safe use of cobalt 60 gamma irradiation. Also presented are some of the many initiatives undertaken at MDS Nordion. Topics covered include our investment for the future supply of raw materials and the latest news from source production. Briefly presented are the tasks associated with the safe transport of cobalt 60 around the world. Discussed is cobalt 60 usage at the customer site; more specifically maintaining source integrity, source utilization and irradiator design trends. Highlighted are industry trends for North America, Europe and the rest of the world. Finally presented are the challenges and opportunities for the industry. Stressed in the paper is the need to work together

Hard hardfacing by welding in the manufacture of valves; Problem Cobalt, alternatives, advantages, disadvantages

International Nuclear Information System (INIS)

Piquer Caballero, J.

2014-01-01

Alloys of recharge usually used in the field of the valves are base alloys cobalt (stellite), but in the field of nuclear power plants, due to radioactive activation of the cobalt, there is a growing trend to replace these alloys with other calls cobalt free . In this paper we will explore the most frequent and will be deducted the relevant advantages and disadvantages of these, in comparison with base alloys cobalt. (Author)

Synthesis of nanocrystalline cobalt ferrite through soft chemistry methods: A green chemistry approach using sesame seed extract

Energy Technology Data Exchange (ETDEWEB)

Gingasu, Dana [Ilie Murgulescu Institute of Physical Chemistry, Romanian Academy, 202 Splaiul Independentei, 060021, Bucharest (Romania); Mindru, Ioana, E-mail: imandru@yahoo.com [Ilie Murgulescu Institute of Physical Chemistry, Romanian Academy, 202 Splaiul Independentei, 060021, Bucharest (Romania); Mocioiu, Oana Catalina; Preda, Silviu; Stanica, Nicolae; Patron, Luminita [Ilie Murgulescu Institute of Physical Chemistry, Romanian Academy, 202 Splaiul Independentei, 060021, Bucharest (Romania); Ianculescu, Adelina; Oprea, Ovidiu [Politehnica University of Bucharest, Faculty of Chemistry, 1-7 Polizu Street, 011061, Bucharest (Romania); Nita, Sultana; Paraschiv, Ileana [National Institute for Chemical Pharmaceutical Research and Development, 112 Calea Vitan, 031299, Bucharest (Romania); Popa, Marcela; Saviuc, Crina [University of Bucharest, Faculty of Biology, Microbiology Department, Research Institute of the University of Bucharest-ICUB, Life, Environmental and Earth Sciences Division, 91-95 Splaiul Independentei, Bucharest (Romania); Bleotu, Coralia [Stefan S. Nicolau Institute of Virology, Cellular and Molecular Pathology Department, 285 Mihai Bravu Avenue, Bucharest (Romania); Chifiriuc, Mariana Carmen [University of Bucharest, Faculty of Biology, Microbiology Department, Research Institute of the University of Bucharest-ICUB, Life, Environmental and Earth Sciences Division, 91-95 Splaiul Independentei, Bucharest (Romania)

2016-10-01

The nanocrystalline cobalt ferrites (CoFe{sub 2}O{sub 4}) were obtained through self-combustion and wet ferritization methods using aqueous extracts of sesame (Sesamum indicum L) seeds. The multimetallic complex compounds were characterized by Fourier transform infrared spectroscopy (FTIR), UV-VIS spectroscopy and thermal analysis. Phase identification, morphological evolution and magnetic properties of the obtained cobalt ferrites were investigated using X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), FTIR and magnetic measurements. FE-SEM investigations revealed the particle size of CoFe{sub 2}O{sub 4} obtained by wet ferritization method ranged between 3 and 20.45 nm. Their antimicrobial, anti-biofilm and cytotoxic properties were evaluated. - Highlights: • CoFe{sub 2}O{sub 4} were obtained by two chemical synthesis methods. • Sesame seed extract was used as gelling or chelating agent. • The morphological features of CoFe{sub 2}O{sub 4} nanoparticles were evaluated. • CoFe{sub 2}O{sub 4} exhibited good microbicidal and anti-biofilm features.

Aluminium - Cobalt-Pillared Clay for Dye Filtration Membrane

Science.gov (United States)

Darmawan, A.; Widiarsih

2018-04-01

The manufacture of membrane support from cobalt aluminium pillared clay has been conducted. This research was conducted by mixing a clay suspension with pillared solution prepared from the mixture of Co(NO3)2.6H2O and AlCl3.6H2O. The molar ratio between Al and Co was 75:25 and the ratio of [OH-]/[metal] was 2. The clay suspension was stirred for 24 hours at room temperature, filtered and dried. The dried clay was then calcined at 200°C, 300°C and 400°C with a ramp rate of 2°C/min. Aluminium-cobalt-pillared clay was then characterized by XRD and GSA and moulded become a membrane support for subsequent tests on dye filtration. The XRD analysis showed that basal spacing (d 001) value of aluminium cobalt was 19.49 Å, which was higher than the natural clay of 15.08Å however, the basal spacing decreased with increasing calcination temperature. The result of the GSA analysis showed that the pore diameter of the aluminium cobalt pillared clay membrane was almost the same as that of natural clay that were 34.5Å and 34.2Å, respectively. Nevertheless, the pillared clay has a more uniform pore size distribution. The results of methylene blue filtration measurements demonstrated that the membrane filter support could well which shown by a clear filtrate at all concentrations tested. The value of rejection and flux decreased with the increasing concentration of methylene blue. The values of dye rejection and water flux reached 99.89% and 5. 80 x 10-6 kg min-1, respectively but they decreased with increasing concentration of methylene blue. The results of this study indicates that the aluminium-pillared clay cobalt could be used as membrane materials especially for ultrafiltration.

Application of Two Cobalt-Based Metal-Organic Frameworks as Oxidative Desulfurization Catalysts.

Science.gov (United States)

Masoomi, Mohammad Yaser; Bagheri, Minoo; Morsali, Ali

2015-12-07

Two new porous cobalt-based metal-organic frameworks, [Co6(oba)5(OH)2(H2O)2(DMF)4]n · 5DMF (TMU-10) and [Co3(oba)3(O) (Py)0.5] n · 4DMF · Py (TMU-12) have been synthesized by solvothermal method using a nonlinear dicarboxylate ligand. Under mild reaction conditions, these compounds exhibited good catalytic activity and reusability in oxidative desulfurization (ODS) reaction of model oil which was prepared by dissolving dibenzothiophene (DBT) in n-hexane. FT-IR and Mass analysis showed that the main product of DBT oxidation is its corresponding sulfone, which was adsorbed on the surfaces of catalysts. The activation energy was obtained as 13.4 kJ/mol.

Monsoon induced cobalt enrichment in Porites (coral) from the Arabian Sea

Digital Repository Service at National Institute of Oceanography (India)

Naqvi, S.A.S.; Nath, B.N.

Cobalt concentrations in growth bands of a reef building coral (Porites sp.) collected from Kalpeni Atoll of the Lakshadweep group of islands (Arabian Sea), rvealed that cobalt concentrations and Co/Ca ratios exhibit similar trend. Study indicates...

Fabrication, microstructure, and mechanical properties of high strength cobalt sub-micron structures

International Nuclear Information System (INIS)

Jin Sumin; Burek, Michael J.; Evans, Robert D.; Jahed, Zeinab; Leung, Michael C.; Evans, Neal D.; Tsui, Ting Y.

2012-01-01

The mechanical properties exhibited by sub-micron scale columnar structures of cobalt, fabricated by electron beam lithography and electroplating techniques, were investigated through uniaxial compression. Transmission electron microscopy analyses show these specimens possess a microstructure with sub-micron grains which are elongated and aligned near to the pillar loading axis. In addition, small nanocrystalline cobalt crystals are also present within the columnar structure. These specimens display exceptional mechanical strength comparable with both bulk polycrystalline and nanocrystalline cobalt deposited by electroplating. Size-dependent softening with shrinking sample dimensions is also observed in this work. Additionally, the strength of these sub-micron structures appears to be strain rate sensitive and comparable with bulk nanocrystalline cobalt specimens.

Cobalt doped proangiogenic hydroxyapatite for bone tissue engineering application.

Science.gov (United States)

Kulanthaivel, Senthilguru; Roy, Bibhas; Agarwal, Tarun; Giri, Supratim; Pramanik, Krishna; Pal, Kunal; Ray, Sirsendu S; Maiti, Tapas K; Banerjee, Indranil

2016-01-01

The present study delineates the synthesis and characterization of cobalt doped proangiogenic-osteogenic hydroxyapatite. Hydroxyapatite samples, doped with varying concentrations of bivalent cobalt (Co(2+)) were prepared by the ammoniacal precipitation method and the extent of doping was measured by ICP-OES. The crystalline structure of the doped hydroxyapatite samples was confirmed by XRD and FTIR studies. Analysis pertaining to the effect of doped hydroxyapatite on cell cycle progression and proliferation of MG-63 cells revealed that the doping of cobalt supported the cell viability and proliferation up to a threshold limit. Furthermore, such level of doping also induced differentiation of the bone cells, which was evident from the higher expression of differentiation markers (Runx2 and Osterix) and better nodule formation (SEM study). Western blot analysis in conjugation with ELISA study confirmed that the doped HAp samples significantly increased the expression of HIF-1α and VEGF in MG-63 cells. The analysis described here confirms the proangiogenic-osteogenic properties of the cobalt doped hydroxyapatite and indicates its potential application in bone tissue engineering. Copyright © 2015 Elsevier B.V. All rights reserved.

Development of wear-resistant coatings for cobalt-base alloys

International Nuclear Information System (INIS)

Cockeram, B.V.

1999-01-01

The costs and hazards resulting from nuclear plant radiation exposure with activated cobalt wear debris could potentially be reduced by covering the cobalt-base materials with a wear resistant coating. However, the hardnesses of many cobalt-base wear alloys are significantly lower than conventional PVD hard coatings, and mechanical support of the hard coating is a concern. Four approaches have been taken to minimize the hardness differences between the substrate and PVD hard coating: (1) use a thin Cr-nitride hard coating with layers that are graded with respect to hardness, (2) use a thicker, multilayered coating (Cr-nitride or Zr-nitride) with graded layers, (3) use nitriding to harden the alloy subsurface followed by application of a multilayered coating of Cr-nitride, and (4) use of nitriding alone. Since little work has been done on application of PVD hard coatings to cobalt-base alloys, some details on process development and characterization of the coatings is presented. Scratch testing was used to evaluate the adhesion of the different coatings. A bench-top rolling contact test was used to evaluate the wear resistance of the coatings. The test results are discussed, and the more desirable coating approaches are identified

Band metamagnetism and peculiarities of magnetic structure of (Er1-xYx)Co2 compounds

International Nuclear Information System (INIS)

Baranov, N.V.; Kozlov, A.I.; Pirogov, A.N.; Sinitsyn, E.V.

1989-01-01

A study of the magnetization, electric resistance, and thermal expansion as well as neutron diffraction data are used to show that in Er 1-x Y x Co 2 compounds the splitting of the d=zone of cobalt disappears as yttrium concentration grows up to x=0.4 and that simultaneously disordering of the Er subssystem sets in due to a phase transition of the first kind. It is discovered that at x∼0.45 the introduction of a weak external magnetic field with μ 0 H∼0.4 T causes the magnetization of the partially disordered Er subsystem to grow, which is accompanied by an irreversible splitting of the d-zone and an increase in the magnetic moment of cobalt from 0.3μ B to 0.9μ B . The presence of minima on the temperature curves for the electric resistance, observed in Er 1-x Y x Co 2 compounds (.2≤x≤0.6) at temperatures above the magnetic ordering temperature, is related to spin density fluctuations in the Co subsystem

Molecular, crystal, and electronic structure of the cobalt(II) complex with 10-(2-benzothiazolylazo)-9-phenanthrol

Energy Technology Data Exchange (ETDEWEB)

Linko, R. V., E-mail: rlinko@mail.ru [Peoples' Friendship University of Russia (Russian Federation); Sokol, V. I. [Russian Academy of Sciences, Kurnakov Institute of General and Inorganic Chemistry (Russian Federation); Polyanskaya, N. A.; Ryabov, M. A.; Strashnov, P. V.; Davydov, V. V. [Peoples' Friendship University of Russia (Russian Federation); Sergienko, V. S. [Russian Academy of Sciences, Kurnakov Institute of General and Inorganic Chemistry (Russian Federation)

2013-05-15

The reaction of 10-(2-benzothiazolylazo)-9-phenanthrol (HL) with cobalt(II) acetate gives the coordination compound [CoL{sub 2}] {center_dot} CHCl{sub 3} (I). The molecular and crystal structure of I is determined by X-ray diffraction. The coordination polyhedron of the Co atom in complex I is an octahedron. The anion L acts as a tridentate chelating ligand and is coordinated to the Co atom through the phenanthrenequinone O1 atom and the benzothiazole N1 atom of the moieties L and the N3 atom of the azo group to form two five-membered metallocycles. The molecular and electronic structures of the compounds HL, L, and CoL{sub 2} are studied at the density functional theory level. The results of the quantum-chemical calculations are in good agreement with the values determined by X-ray diffraction.

Molecular, crystal, and electronic structure of the cobalt(II) complex with 10-(2-benzothiazolylazo)-9-phenanthrol

International Nuclear Information System (INIS)

Linko, R. V.; Sokol, V. I.; Polyanskaya, N. A.; Ryabov, M. A.; Strashnov, P. V.; Davydov, V. V.; Sergienko, V. S.

2013-01-01

The reaction of 10-(2-benzothiazolylazo)-9-phenanthrol (HL) with cobalt(II) acetate gives the coordination compound [CoL 2 ] · CHCl 3 (I). The molecular and crystal structure of I is determined by X-ray diffraction. The coordination polyhedron of the Co atom in complex I is an octahedron. The anion L acts as a tridentate chelating ligand and is coordinated to the Co atom through the phenanthrenequinone O1 atom and the benzothiazole N1 atom of the moieties L and the N3 atom of the azo group to form two five-membered metallocycles. The molecular and electronic structures of the compounds HL, L, and CoL 2 are studied at the density functional theory level. The results of the quantum-chemical calculations are in good agreement with the values determined by X-ray diffraction.

Sulfur, cobalt and europium activation from the A-bombs in Japan

International Nuclear Information System (INIS)

Gritzner, M.L.; Egbert, S.D.; Woolson, W.A.

1987-01-01

Comparisons are made between calculations and measurements of in-situ sulfur, cobalt, and europium activation by neutrons at Hiroshima and Nagasaki to check the validity of the neutron sources and transport air-over-ground used in the new Dosimetry System 1986 (DS86). Europium and cobalt are activated by epithermal/thermal neutrons. The sulfur activation has an effective threshold around 2 MeV. Comparisons of sulfur activation at Hiroshima, which necessitate considering the tilt and heading of the cylindrically shaped Little Boy bomb, confirm the high energy neutron portion of the source relevant to sulfur activation. The europium and cobalt activation calculations tend to be higher than the measurements for ground ranges within 300 m and lower than the measurements beyond 700 m. Thus, the cobalt and europium measurements do not validate the source or the transport, embodied in DS87, for those neutrons relevant to europium and cobalt activation. Presently, it is unresolved as to whether the discrepancy can be explained as a problem in the measurements, in their interpretation, or as a problem in the calculations due to the source neutrons and/or their transport from source to the sample site

Cobalt doped proangiogenic hydroxyapatite for bone tissue engineering application

Energy Technology Data Exchange (ETDEWEB)

Kulanthaivel, Senthilguru [Department of Biotechnology and Medical Engineering, National Institute of Technology, Rourkela, Odisha 769008 (India); Roy, Bibhas [Department of Biotechnology, Indian Institute of Technology Kharagpur, Kharagpur, West Bengal 721302 (India); Agarwal, Tarun [Department of Biotechnology and Medical Engineering, National Institute of Technology, Rourkela, Odisha 769008 (India); Giri, Supratim [Department of Chemistry, National Institute of Technology, Rourkela, Odisha 769008 (India); Pramanik, Krishna; Pal, Kunal; Ray, Sirsendu S. [Department of Biotechnology and Medical Engineering, National Institute of Technology, Rourkela, Odisha 769008 (India); Maiti, Tapas K. [Department of Biotechnology, Indian Institute of Technology Kharagpur, Kharagpur, West Bengal 721302 (India); Banerjee, Indranil, E-mail: indraniliit@gmail.com [Department of Biotechnology and Medical Engineering, National Institute of Technology, Rourkela, Odisha 769008 (India)

2016-01-01

ABSTRACT: The present study delineates the synthesis and characterization of cobalt doped proangiogenic–osteogenic hydroxyapatite. Hydroxyapatite samples, doped with varying concentrations of bivalent cobalt (Co{sup 2+}) were prepared by the ammoniacal precipitation method and the extent of doping was measured by ICP–OES. The crystalline structure of the doped hydroxyapatite samples was confirmed by XRD and FTIR studies. Analysis pertaining to the effect of doped hydroxyapatite on cell cycle progression and proliferation of MG-63 cells revealed that the doping of cobalt supported the cell viability and proliferation up to a threshold limit. Furthermore, such level of doping also induced differentiation of the bone cells, which was evident from the higher expression of differentiation markers (Runx2 and Osterix) and better nodule formation (SEM study). Western blot analysis in conjugation with ELISA study confirmed that the doped HAp samples significantly increased the expression of HIF-1α and VEGF in MG-63 cells. The analysis described here confirms the proangiogenic–osteogenic properties of the cobalt doped hydroxyapatite and indicates its potential application in bone tissue engineering. - Highlights: • Cobalt (Co{sup +2}) doped hydroxyapatite (Co-HAp) can be prepared by the wet chemical method. • The concentration of Co{sup +2} influences the physico-chemical properties of HAp. • Co-HAp was found to be biocompatible and osteogenic. • Co-HAp enhanced cellular VEGF secretion through HIF-1α stabilization. • The optimum biological performance of Co-HAp was achieved for 0.33% (w/w) Co{sup +2} doping.

Development of wear-resistant coatings for cobalt-base alloys

International Nuclear Information System (INIS)

Cockeram, B.V.

1999-01-01

The level of nuclear plant radiation exposure due to activated cobalt wear debris could potentially be reduced by covering the cobalt-base materials with a wear resistant coating. Laboratory pin-on-disc and rolling contact wear tests were used to evaluate the wear performance of several coatings. Based on the results of these tests, multilayer Cr-nitride coatings and ion nitriding are the most promising approaches

HLA -A, -B, -C and -DR antigens in individuals with sensitivity to cobalt

Energy Technology Data Exchange (ETDEWEB)

Fischer, T; Rystedt, I; Saefwenberg, J; Egle, I

1984-01-01

In a skin investigation of 853 individuals working with hard metal manufacturing 39 cases of cobalt allergy were found. Thirty-five of the individuals with cobalt sensitivity and 102 matched controls were HLA-A, -B, -C and -DR typed. No significantly deviating HLA antigen frequencies were observed when the two groups were compared. Thus, there are no signs that a certain HLA antigen would dispose to cobalt allergy. In the cobalt sensitive group the B7 positive individuals showed particularly often simultaneous reactions to other contact allergens. The B12 positive individuals had low reactivity while the A28 positive showed high reactivity.

Cobalt release and complications resulting from the use of dental prostheses

DEFF Research Database (Denmark)

Al-Imam, Hiba; Benetti, Ana R.; Özhayat, Esben B.

2016-01-01

of the functional prostheses released cobalt, whereas this was observed in 24 of 32 non-functional prostheses. None of the patients had contact allergy to cobalt. Of the 66 patients, 11 showed signs of inflammation of the oral mucosa, 2 had oral candidiasis, 16 had ill-fitting prostheses, and all had insufficient...... oral hygiene. CONCLUSIONS: Dental prostheses released cobalt during the fabrication stages, but not 1-5 years after insertion. No allergic reactions were observed. Signs of inflammation were related to candidiasis, insufficient oral hygiene, and ill-fitting prostheses....

Cobalt deficiency effects on trace elements, hormones and enzymes involved in energy metabolism of cattle.

Science.gov (United States)

Stangl, G I; Schwarz, F J; Kirchgessner, M

1999-03-01

This study was conducted to investigate the physiological consequences of long-term moderate cobalt deficiency in beef cattle, which have not hitherto been studied in detail. Cobalt deficiency was induced in cattle by feeding two groups of animals either a basal corn silage-based diet that was moderately low in cobalt (83 micrograms Co/kg), or the same diet supplemented with cobalt to a total of 200 micrograms per kg, for 43 weeks. Cobalt deficiency was induced, as judged by inappetance, diminished growth gain and a markedly reduced vitamin B12 status in serum and liver. The long-term cobalt deprivation which was primarily a combination of reduced feed intake and a tissue vitamin B12 deficiency did not show evidence of a significant dysfunction of energy metabolism. The activities of glucose-6-phosphate dehydrogenase and cytochrome oxidase in liver remained unaffected by cobalt deficiency, nor was there a significant change in serum glucose level of cattle on the cobalt-deprived diet. However, analysis of thyroid hormone status indicated a slight reduction of type I thyroxine monodeiodinase activity in liver accompanied by a significant reduction of the triiodothyronine level in serum. The diminished liver vitamin B12 level resulted in significantly reduced folate level in this tissue, reduced concentrations of heme-depending blood parameters. Moreover cobalt deficiency or rather vitamin B12 deficiency was accompanied by a dramatic accumulation of the trace elements iron and nickel in liver. These results indicate that long-term moderate cobalt deficiency may induce a number of physiological changes in cattle, but a follow-up study, which excluded different feed levels by including a pair-fed control group, will be necessary to actually obtain the single effect of cobalt deficiency in cattle.

Effect of Cobalt Source on the Catalyst Reducibility and Activity of ...

African Journals Online (AJOL)

The effect of cobalt precursor (nitrate, acetate and chloride salts) on the catalyst reducibility and dispersion, ... balt catalysts (>5.0 wt%) prepared using ammonium cobalt ... heated from 323 K to 1073 K using a heating ramp of 10 K min–1.

Self-powered in-core detectors of cobalt type

International Nuclear Information System (INIS)

Jonsson, Georg

1975-01-01

Testing and development of self-powered neutron detectors with a cobalt emitter is described. Long term irradiation at 400 deg C is expected to indicate insulation quality, change in calibration and 60 Co build-up. Dynamic tests to investigate possible transient effects due to temperature changes are being performed on a number of detectors up to about 600 deg C. A long term irradiation at low temperature has been terminated after 4.5 years. On completion, neutron dose was estimated to be 5.6 x 10 21 nvt and the 60 Co background was 9.3 % of the full flux signal. A recently introduced long term test is expected to provide data on instability effects due to 61 Co. For a BWR in-core detector installation, the main advantage of cobalt detectors, apart from the small size, appears to be long life. Development work is being done on detectors with vanadium-cobalt emitters, electronic separation of fast and delayed signals and reduction of gamma sensitivity. (O.T.)

Mechanizm of propylene oxidation on modified cobalt-molybdenum catalysts

International Nuclear Information System (INIS)

Kutyrev, M.Yu.; Rozentuller, B.V.; Isaev, O.V.; Margolis, L.Ya.; Krylov, O.V.

1977-01-01

Effect is studied of additions of iron, copper, nickel, and vanadium oxides, introduced into cobalt, molybdate, on oxidation reactions of propylene to acrolein and acrylicacid. The principal parameters determining the activity and selectivity of oxidation of propylene and acrolein on modified cobalt molibdate are the structure, the type of Mo-O bond, and the nature of the electron transitions in the solid under the effect of adsorption of the reaction components

Valence control of cobalt oxide thin films by annealing atmosphere

Energy Technology Data Exchange (ETDEWEB)

Wang Shijing [School of Materials Science and Engineering, University of Science and Technology Beijing, No. 30 Xueyuan Road, Beijing 100083 (China); Zhang Boping, E-mail: bpzhang@ustb.edu.cn [School of Materials Science and Engineering, University of Science and Technology Beijing, No. 30 Xueyuan Road, Beijing 100083 (China); Zhao Cuihua; Li Songjie; Zhang Meixia; Yan Liping [School of Materials Science and Engineering, University of Science and Technology Beijing, No. 30 Xueyuan Road, Beijing 100083 (China)

2011-02-01

The cobalt oxide (CoO and Co{sub 3}O{sub 4}) thin films were successfully prepared using a spin-coating technique by a chemical solution method with CH{sub 3}OCH{sub 2}CH{sub 2}OH and Co(NO{sub 3}){sub 2}.6H{sub 2}O as starting materials. The grayish cobalt oxide films had uniform crystalline grains with less than 50 nm in diameter. The phase structure is able to tailor by controlling the annealing atmosphere and temperature, in which Co{sub 3}O{sub 4} thin film was obtained by annealing in air at 300-600, and N{sub 2} at 300, and transferred to CoO thin film by raising annealing temperature in N{sub 2}. The fitted X-ray photoelectron spectroscopy (XPS) spectra of the Co2p electrons are distinguishable from different valence states of cobalt oxide especially for their satellite structure. The valence control of cobalt oxide thin films by annealing atmosphere contributes to the tailored optical absorption property.

Raman analysis of cobalt blue pigment in blue and white porcelain: A reassessment

Science.gov (United States)

Jiang, Xiaochenyang; Ma, Yanying; Chen, Yue; Li, Yuanqiu; Ma, Qinglin; Zhang, Zhaoxia; Wang, Changsui; Yang, Yimin

2018-02-01

Cobalt blue is a famous pigment in human history. In the past decade it is widely reported that the cobalt aluminate has been detected in ancient ceramics as blue colorant in glaze, yet the acquired Raman spectra are incredibly different from that of synthesised references, necessitating a reassessment of such contradictory scenario with more accurate analytic strategies. In this study, micro-Raman spectroscopy (MRS) and scanning electron microscopy (SEM) in association with energy dispersive spectrometry (EDS) were performed on under-glaze cobalt pigments from one submerged blue and white porcelain shard dated from Wanli reign (1573-1620 CE) of Ming dynasty (1365-1644 CE) excavated at Nan'ao I shipwreck off the southern coast of China. The micro-structural inspection reveals that the pigment particles have characteristics of small account, tiny size, heterogeneously distribution, and more importantly, been completely enwrapped by well-developed anorthite crystals in the glaze, indicating that the signals recorded in previous publications are probably not from cobalt pigments themselves but from outside thickset anorthite shell. The further spectromicroscopic analyses confirm this presumption when the accurate spectra of cobalt aluminate pigment and surrounding anorthite were obtained separately with precise optical positioning. Accordingly, we reassess and clarify the previous Raman studies dedicated to cobalt blue pigment in ancient ceramics, e.g. cobalt blue in celadon glaze, and in turn demonstrate the superiority and necessity of coupling spectroscopic analysis with corresponding structure observation, especially in the characterization of pigments from complicated physico-chemical environment like antiquities. Thus, this study promotes a better understanding of Raman spectroscopy study of cobalt blue pigments in art and archaeology field.

Preparation of rare earth-cobalt magnet alloy by reduction-diffusion process

International Nuclear Information System (INIS)

Krishnan, T.S.

1980-01-01

Preparation of rare earth-cobalt alloys by reduction-diffusion (R-D) process is described. The process essentially involves mixing of the rare earth oxide and cobalt/cobalt oxide powders in proper proportion and high temperature reduction of the charge in hydrogen atmosphere, followed by aqueous leaching of the reduced mass to yield the alloy powder. Comparison is made of the magnetic properties of the R-D powder with those of the powder prepared by the direct melting (DM) route and it is observed from the reported values for SmCo 5 that the energy product of the R-D powder (approximately 22 MGOe) is only marginally lower than that of the directly melted alloy (approximately 25 MGOe). The paper also includes the results of studies carried out at the Bhabha Atomic Research Centre, Bombay, on the preparation of misch metal-cobalt alloy by the R-D process. (auth.)

Magnetic and resonance properties of ferrihydrite nanoparticles doped with cobalt

Science.gov (United States)

Stolyar, S. V.; Yaroslavtsev, R. N.; Iskhakov, R. S.; Bayukov, O. A.; Balaev, D. A.; Dubrovskii, A. A.; Krasikov, A. A.; Ladygina, V. P.; Vorotynov, A. M.; Volochaev, M. N.

2017-03-01

Powders of undoped ferrihydrite nanoparticles and ferrihydrite nanoparticles doped with cobalt in the ratio of 5: 1 have been prepared by hydrolysis of 3 d-metal salts. It has been shown using Mössbauer spectroscopy that cobalt is uniformly distributed over characteristic crystal-chemical positions of iron ions. The blocking temperatures of ferrihydrite nanoparticles have been determined. The nanoparticle sizes, magnetizations, surface anisotropy constants, and bulk anisotropy constants have been estimated. The doping of ferrihydrite nanoparticles with cobalt leads to a significant increase in the anisotropy constant of a nanoparticle and to the formation of surface rotational anisotropy with the surface anisotropy constant K u = 1.6 × 10-3 erg/cm2.

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

International Nuclear Information System (INIS)

Gruner, B.; Plesek, J.; Baca, J.; Cisarova, I.; Dozol, J.F.; Rouquette, H.; Vinas, C.; Selucky, P.; Rais, J.

2002-01-01

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

Extraction spectrophotometric determination of elements in form of ion-association compounds of metal chaltes and dyes. Pt. 2. The system cobalt-5, 7-dichloro-8-hydroxyquinoline-rhodamine 6G, benzene

International Nuclear Information System (INIS)

Minczewski, J.; Chwastowska, J.; Lachowicz, E.

1976-01-01

The extraction of the ion-pair formed by the anionic, coordinatively saturated complex of cobalt with 5,7-dichloro-8-hydroxyquinoline (Cl 2 HOx) and Rhodamine 6G cation (ROD + ) was investigated. The cobalt ions at the concentration 4 x 10 -5 M are fully extractable at pH=6.3; 1 x 10 -3 M Cl 2 HOx and 4 x 10 -4 M Rhodamine 6G after 10 minutes of extraction. In absence of Rhodamine 6G the cobalt complexes are not extractable. The extractable ion-pair has the composition according to the formula Co(Cl 2 Ox) 3 - .ROD + . The molar absorptivity at lambda=542 nm is equal to 7.5 x 10 4 . The extraction constant log Ksub(ex)=0.44+-0.14. The protonation constant of Rhodamine (log K=-0.98+-0.08) and two-phase stability constant of the carbinol base of Rhodamine 6G (log β = 5.35. +- 0.04) were also calculated. (author)

Competitive Adsorption-Assisted Formation of One-Dimensional Cobalt Nanochains with High CO Hydrogenation Activity

Energy Technology Data Exchange (ETDEWEB)

Liang, Xin [State; Ren, Zhibo [State; Institute; Zhu, Xiaolin [State; Zhang, Qinwei [State; Mei, Donghai [Institute; Chen, Biaohua [State

2017-10-31

In the present work, cobalt nanochains have been successfully synthesized by a novel co assisted self-assembling formation strategy. A dramatic morphology transformation from cobalt nanoparticles to nanochains are observed when co molecules were introduced into the synthetic system. DFT calculations further confirm that competitive co-adsorbed co and oleylamine over the cobalt nanoparticles facilitates the formation of cobalt nanochains, which show higher co hydrogenation performance. The present work provides a new strategic and promising method for controllable synthesis of catalyst nanomaterials with the preferred surface structure and morphology.

Research about combination of Gamma Knife and cobalt-60 radiation therapy to treat hypophysoma

International Nuclear Information System (INIS)

Xing Yueming; Zhao Xinping; Song Xiang; Wu Wei; Huang Bai

2003-01-01

Objective: To probe the therapeutic effectiveness of combination of Gamma Knife and cobalt-60 radiotherapy. Methods: 80 Hypophysoma patients who have been randomly grouped into two groups. Combination of Gamma Knife and cobalt-60 radiotherapy group and single Gamma knife group. Results: The therapeutic effectiveness of combination of Gamma Knife and cobalt-60 radiation therapy group was higher than that of single Gamma Knife group. Conclusion: The hospital that treat Hypophysoma with single Gamma Knife should add cobalt-60 radiotherapy in order to increase the local Hypophysoma dose

Cobalt (III) complexes as novel matrix metalloproteinase-9 inhibitors

International Nuclear Information System (INIS)

Lee, Jiyoun

2012-01-01

We have synthesized a series of novel MMP-9 inhibitors containing cobalt(III) complexes. The synthesized cobalt(III) complexes are effective as enzyme inhibitors and the attachment of a biphenyl group enhanced the efficiency of enzyme inhibition up to 6-fold. When compared to the reported non-hydroxamate MMP inhibitors, the synthesized complexes showed comparable in vitro potency. The enzyme assay showed that the cobalt(III) complex can disrupt the zinc binding active site of MMP-9 and is proposed to work via a ligand exchange mechanism. Since histidine residues are essential for the catalytic activity of a large percentage of enzymes and zinc finger proteins, these cobalt(III) complexes can serve as a prototype inhibitor towards various zinc containing enzymes and proteins. Matrix metalloproteinases (MMPs) are a family of zinc binding endopeptidases that play crucial roles in various physiological processes and diseases such as embryogenic growth, angiogenesis, arthritis, skin ulceration, liver fibrosis and tumor metastasis. Because of their implications in a wide range of diseases, MMPs are considered as intriguing drug targets. The majority of MMP inhibitors are organic small molecules containing a hydroxamate functionality for the zinc binding group. This hydroxamate group binds to a zinc(II) center in a bidentate fashion and creates a distorted trigonal bipyramidal geometry

Cobalt (III) complexes as novel matrix metalloproteinase-9 inhibitors

Energy Technology Data Exchange (ETDEWEB)

Lee, Jiyoun [Sungshin Women' s Univ., Seoul (Korea, Republic of)

2012-04-15

We have synthesized a series of novel MMP-9 inhibitors containing cobalt(III) complexes. The synthesized cobalt(III) complexes are effective as enzyme inhibitors and the attachment of a biphenyl group enhanced the efficiency of enzyme inhibition up to 6-fold. When compared to the reported non-hydroxamate MMP inhibitors, the synthesized complexes showed comparable in vitro potency. The enzyme assay showed that the cobalt(III) complex can disrupt the zinc binding active site of MMP-9 and is proposed to work via a ligand exchange mechanism. Since histidine residues are essential for the catalytic activity of a large percentage of enzymes and zinc finger proteins, these cobalt(III) complexes can serve as a prototype inhibitor towards various zinc containing enzymes and proteins. Matrix metalloproteinases (MMPs) are a family of zinc binding endopeptidases that play crucial roles in various physiological processes and diseases such as embryogenic growth, angiogenesis, arthritis, skin ulceration, liver fibrosis and tumor metastasis. Because of their implications in a wide range of diseases, MMPs are considered as intriguing drug targets. The majority of MMP inhibitors are organic small molecules containing a hydroxamate functionality for the zinc binding group. This hydroxamate group binds to a zinc(II) center in a bidentate fashion and creates a distorted trigonal bipyramidal geometry.

Cation distributions on rapidly solidified cobalt ferrite

Science.gov (United States)

De Guire, Mark R.; Kalonji, Gretchen; O'Handley, Robert C.

1990-01-01

The cation distributions in two rapidly solidified cobalt ferrites have been determined using Moessbauer spectroscopy at 4.2 K in an 8-T magnetic field. The samples were obtained by gas atomization of a Co0-Fe2O3-P2O5 melt. The degree of cation disorder in both cases was greater than is obtainable by cooling unmelted cobalt ferrite. The more rapidly cooled sample exhibited a smaller departure from the equilibrium cation distribution than did the more slowly cooled sample. This result is explained on the basis of two competing effects of rapid solidification: high cooling rate of the solid, and large undercooling.

Determination of chromium, cobalt and nickel in tissue samples by radiochemical activation analysis

International Nuclear Information System (INIS)

Reisell, A.; Lakomaa, E.L.

1983-03-01

A radiochemical neutron activation analysis method for the determination of chromium, cobalt and nickel in tissue samples. A radiochemical neutron activation analysis method for the determination of chromium, cobalt and nickel has been developed. The destruction device used consisted of a combined wet-ashing-distillation and ion-exchange system. Six samples could be treated at the same time. The samples were wet-ashed with H*L2SO*L4-H*L2O*L2 mixture. Volatile elements were distilled as bromide compounds with HBr*H-. The distillation residue in 8M HCl was passed through hydrated antimony pentoxide (HAP) in order to remove disturbing *H2*H4Na-activity and through a Dowex 2 x 8 column so as to retain *H6*H0Co (formed from *H5*H8Ni). Chromium was elutriated from the column and precipitated as Cr(OH)*L3 for the removal of disturbing *H3*H2P-activity. The standards and samples were treated in a similar manner each so that the yield determination is not necessarily needed. The yields by tracer experiments were (43 +- 5) % for Cr, (93 +- 4) % for Co and (88 +- 14) % for Ni. The precision and accuracy of the method were studied by using reference materials of the National Bureau of Standards (NBS) and the International Atomic Energy Agency (IAEA)

An Economic Analysis of Electron Accelerators and Cobalt-60 for Irradiating Food

OpenAIRE

Morrison, Rosanna Mentzer

1989-01-01

Average costs per pound of irradiating food are similar for the electron accelerator and cobalt-60 irradiators analyzed in this study, but initial investment costs can vary by $1 million. Irradiation costs range from 0.5 to 7 cents per pound and decrease as annual volumes treated increase. Cobalt-60 is less expensive than electron beams for annual volumes below 50 million pounds. For radiation source requirements above the equivalent of 1 million curies of cobalt-60, electron beams are more e...

Dose-dependent cytotoxicity of clinically relevant cobalt nanoparticles and ions on macrophages in vitro

Energy Technology Data Exchange (ETDEWEB)

Kwon, Young-Min; Xia Zhidao; Glyn-Jones, Sion; Beard, David; Gill, Harinderjit S; Murray, David W, E-mail: young-min.kwon@ndos.ox.ac.u [Nuffield Department of Orthopaedic Surgery, University of Oxford, Oxford OX3 7LD (United Kingdom)

2009-04-15

Despite the satisfactory short-term implant survivorship of metal-on-metal hip resurfacing arthroplasty, periprosthetic soft-tissue masses such as pseudotumours are being increasingly reported. Cytotoxic effects of cobalt or chromium have been suggested to play a role in its aetiology. The aim of this study was to investigate the effects of clinically relevant metal nanoparticles and ions on the viability of macrophages in vitro. A RAW 264.7 murine macrophage cell line was cultured in the presence of either: (1) cobalt, chromium and titanium nanoparticles sized 30-35 nm; or (2) cobalt sulphate and chromium chloride. Two methods were used to quantify cell viability: Alamar Blue assay and Live/Dead assay. The cytotoxicity was observed only with cobalt. Cobalt nanoparticles and ions demonstrated dose-dependent cytotoxic effects on macrophages in vitro: the cytotoxic concentrations of nanoparticles and ions were 1 x 10{sup 12} particles ml{sup -1} and 1000 {mu}M, respectively. The high concentration of cobalt nanoparticles required for cytotoxicity of macrophages in vitro suggests that increased production of cobalt nanoparticles in vivo, due to excessive MoM implant wear, may lead to local adverse biological effects. Therefore, cytotoxicity of high concentrations of metal nanoparticles phagocytosed by macrophages located in the periprosthetic tissues may be an important factor in pathogenesis of pseudotumours.

Synthesis of cobalt-containing mesoporous catalysts using the ultrasonic-assisted “pH-adjusting” method: Importance of cobalt species in styrene oxidation

Energy Technology Data Exchange (ETDEWEB)

Li, Baitao, E-mail: btli@scut.edu.cn; Zhu, Yanrun; Jin, Xiaojing

2015-01-15

Cobalt-containing SBA-15 and MCM-41 (Co-SBA-15 and Co-MCM-41) mesoporous catalysts were prepared via ultrasonic-assisted “pH-adjusting” technique in this study. Their physiochemical structures were comprehensively characterized and correlated with catalytic activity in oxidation of styrene. The nature of cobalt species depended on the type of mesoporous silica as well as pH values. The different catalytic performance between Co-SBA-15 and Co-MCM-41 catalysts originated from cobalt species. Cobalt species were homogenously incorporated into the siliceous framework of Co-SBA-15 in single-site Co(II) state, while Co{sub 3}O{sub 4} particles were loaded on Co-MCM-41 catalysts. The styrene oxidation tests showed that the single-site Co(II) state was more beneficial to the catalytic oxidation of styrene. The higher styrene conversion and benzaldehyde selectivity over Co-SBA-15 catalysts were mainly attributed to single-site Co(II) state incorporated into the framework of SBA-15. The highest conversion of styrene (34.7%) with benzaldehyde selectivity of 88.2% was obtained over Co-SBA-15 catalyst prepared at pH of 7.5, at the mole ratio of 1:1 (styrene to H{sub 2}O{sub 2}) at 70 °C. - Graphical abstract: Cobalt-containing mesoporous silica catalysts were developed via ultrasonic-assisted “pH-adjusting” technique. Compared with Co{sub 3}O{sub 4} in Co-MCM-41, the single-site Co(II) state in Co-SBA-15 was more efficient for the styrene oxidation. - Highlights: • Fast and cost-effective ultrasonic technique for preparing mesoporous materials. • Incorporation of Co via ultrasonic irradiation and “pH-adjusting”. • Physicochemical comparison between Co-SBA-15 and Co-MCM-41. • Correlation of styrene oxidation activity and catalyst structural property.

Activation of cobalt by neutrons from the Hiroshima bomb

International Nuclear Information System (INIS)

Kerr, G.D.; Dyer, F.F.; Emery, J.F.; Pace, J.V. III; Brodzinski, R.L.; Marcum, J.

1990-02-01

A study has been completed of cobalt activation in samples from two new locations in Hiroshima. The samples consisted of a piece of steel from a bridge located at a distance of about 1300 m from the hypocenter and pieces of both steel and concrete from a building located at approximately 700 m. The concrete was analyzed to obtain information needed to calculate the cobalt activation in the two steel samples. Close agreement was found between calculated and measured values for cobalt activation of the steel sample from the building at 700 m. It was found, however, that the measured values for the bridge sample at 1300 m were approximately twice the calculated values. Thus, the new results confirm the existence of a systematic error in the transport calculations for neutrons from the Hiroshima bomb. 52 refs., 32 figs., 16 tabs

Synthesis and structural characterization of polyaniline/cobalt chloride composites

Energy Technology Data Exchange (ETDEWEB)

Asha, E-mail: arana5752@gmail.com [Department of Basic and Applied Sciences, Bhagat Phool Singh Mahilla Vishwavidyalaya, Khanpur Kalan, Sonipat-131305 (India); Goyal, Sneh Lata; Kishore, Nawal [Department of Applied Physics, Guru Jambheshwar University of Science and Technology, Hisar-125001 (India)

2016-05-23

Polyaniline (PANI) and PANI /cobalt chloride composites were synthesized by in situ chemical oxidative polymerization of aniline with CoCl{sub 2}.6H{sub 2}O using ammonium peroxidisulphate as an oxidant. These composites were characterized by X-ray diffraction (XRD) and Scanning electron microscopy (SEM). The XRD study reveals that both PANI and composites are amorphous. The XRD and SEM results confirm the presence of cobalt chloride in the composites.

Interface Controlled Oxidation States in Layered Cobalt Oxide Nanoislands on Gold

DEFF Research Database (Denmark)

Walton, Alexander; Fester, Jakob; Bajdich, Michal

2015-01-01

Layered cobalt oxides have been shown to be highly active catalysts for the oxygen evolution reaction (OER; half of the catalytic “water splitting” reaction), particularly when promoted with gold. However, the surface chemistry of cobalt oxides and in particular the nature of the synergistic effect...

Nanofibre growth from cobalt carbide produced by mechanosynthesis

Energy Technology Data Exchange (ETDEWEB)

Diaz Barriga-Arceo, L [Instituto Mexicano del Petroleo, Programa de Ingenieria Molecular, Eje Central Lazaro Cardenas 152, Colonia San Bartolo Atepehuacan, Mexico DF, 07730 (Mexico); Orozco, E [Instituto de Fisica UNAM, Apartado Postal 20-364 CP 01000, DF (Mexico); Garibay-Febles, V [Instituto Mexicano del Petroleo, Programa de Ingenieria Molecular, Eje Central Lazaro Cardenas 152, Colonia San Bartolo Atepehuacan, Mexico DF, 07730 (Mexico); Bucio-Galindo, L [Instituto de Fisica UNAM, Apartado Postal 20-364 CP 01000, DF (Mexico); Mendoza Leon, H [FM-UPALM, IPN, Apartado Postal 75-395 CP 07300, DF (Mexico); Castillo-Ocampo, P [UAM-Iztapalapa, Apartado Postal 55-334 CP 09340, DF (Mexico); Montoya, A [Instituto Mexicano del Petroleo, Programa de Ingenieria Molecular, Eje Central Lazaro Cardenas 152, Colonia San Bartolo Atepehuacan, Mexico DF, 07730 (Mexico)

2004-06-09

Mechanical alloying was used to prepare cobalt carbide. Microstructural characterization of samples was performed by x-ray diffraction, differential scanning calorimetry and transmission electron microscopy methods. In order to produce carbon nanotubes, the cobalt carbide was precipitated after heating at 800 and 1000 deg. C for 10 min. Nanofibres of about 10-50 nm in diameter, 0.04-0.1 {mu}m in length and 20-200 nm in diameter and 0.6-1.2 {mu}m in length were obtained after heating at 800 and 1000 deg. C, respectively, by means of this process.

Nanofibre growth from cobalt carbide produced by mechanosynthesis

International Nuclear Information System (INIS)

Diaz Barriga-Arceo, L; Orozco, E; Garibay-Febles, V; Bucio-Galindo, L; Mendoza Leon, H; Castillo-Ocampo, P; Montoya, A

2004-01-01

Mechanical alloying was used to prepare cobalt carbide. Microstructural characterization of samples was performed by x-ray diffraction, differential scanning calorimetry and transmission electron microscopy methods. In order to produce carbon nanotubes, the cobalt carbide was precipitated after heating at 800 and 1000 deg. C for 10 min. Nanofibres of about 10-50 nm in diameter, 0.04-0.1 μm in length and 20-200 nm in diameter and 0.6-1.2 μm in length were obtained after heating at 800 and 1000 deg. C, respectively, by means of this process

Pressure effects on crystal structures and magnetic properties of RCo{sub 5} (R = Y or Gd) compounds

Energy Technology Data Exchange (ETDEWEB)

Burzo, E. [Faculty of Physics, Babes-Bolyai University Cluj-Napoca 400084 (Romania); Vlaic, P. [Faculty of Physics, Babes-Bolyai University Cluj-Napoca 400084 Romania and University of Medicine and Pharmacy Iuliu Hatieganu, Physics and Biophysics Department Cluj-Napoca (Romania)

2013-11-13

The pressure dependences of crystal structures and magnetic properties of YCo{sub 5} and GdCo{sub 5} compounds are analysed based on band structure calculations. Isomorphic transitions were evidenced for relative volumes v/v{sub 0} = 0.91 and 0.86, for YCo{sub 5} and GdCo{sub 5}, respectively. At the transition, there is a higher decrease of cobalt moments at 3g sites as compared to those located in 2c ones. The induced polarizations on Y4d and Gd5d bands, by short range interactions, are linearly dependent on the magnetizations of cobalt atoms situated in their neighborhood. The isomorphic transitions are analysed in correlations with band structures.

Controllable synthesis of hierarchical nickel cobalt sulfide with enhanced electrochemical activity

Science.gov (United States)

Tie, Jinjin; Han, Jiaxi; Diao, Guiqiang; Liu, Jiwen; Xie, Zhuopeng; Cheng, Gao; Sun, Ming; Yu, Lin

2018-03-01

The composition of nickel cobalt sulfide has great influence on its electrochemical performance. Herein, the nickel cobalt sulfide with different composition and mixed phase were synthesized by one-step solvothermal method through changing the molar ratio of Ni to Co in the reaction system. The electrochemical measurements showed that the nickel cobalt sulfide with a theoretical molar ratio of Ni/Co to be 1.5:1.5 (NCS-2) demonstrates the superior pseudocapacitive performance with a high specific capacitance (6.47 F cm-2 at 10 mA cm-2) and a favorable Coulombic efficiency (∼99%). Whereas, when applied as the catalyst for hydrogen evolution reaction in 1 M KOH aqueous electrolyte, the nickel cobalt sulfide with a theoretical molar ratio of Ni/Co is 1:2 (NCS-1) displays better catalytic activity, and it requires a relatively lower overpotential of 282 mV to deliver the current density of 10 mA cm-2.

Open-Loop Performance of COBALT Precision Landing Payload on a Commercial Sub-Orbital Rocket

Science.gov (United States)

Restrepo, Carolina I.; Carson, John M., III; Amzajerdian, Farzin; Seubert, Carl R.; Lovelace, Ronney S.; McCarthy, Megan M.; Tse, Teming; Stelling, Richard; Collins, Steven M.

2018-01-01

An open-loop flight test campaign of the NASA COBALT (CoOperative Blending of Autonomous Landing Technologies) platform was conducted onboard the Masten Xodiac suborbital rocket testbed. The COBALT platform integrates NASA Guidance, Navigation and Control (GN&C) sensing technologies for autonomous, precise soft landing, including the Navigation Doppler Lidar (NDL) velocity and range sensor and the Lander Vision System (LVS) Terrain Relative Navigation (TRN) system. A specialized navigation filter running onboard COBALT fuses the NDL and LVS data in real time to produce a navigation solution that is independent of GPS and suitable for future, autonomous, planetary, landing systems. COBALT was a passive payload during the open loop tests. COBALT's sensors were actively taking data and processing it in real time, but the Xodiac rocket flew with its own GPS-navigation system as a risk reduction activity in the maturation of the technologies towards space flight. A future closed-loop test campaign is planned where the COBALT navigation solution will be used to fly its host vehicle.

Global gene expression profiling in human lung cells exposed to cobalt

Energy Technology Data Exchange (ETDEWEB)

Malard, V.; Berenguer, F.; Prat, O.; Ruat, S.; Steinmetz, G.; Quemeneur, E. [CEA VALRHO, Serv Biochim and Toxicol Nucl, DSV, iBEB, F-30207 Bagnols Sur Ceze (France)

2007-06-06

It has been estimated that more than 1 million workers in the United States are exposed to cobalt. Occupational exposure to {sup 59}Co occurs mainly via inhalation and leads to various lung diseases. Cobalt is classified by the IARC as a possible human carcinogen (group 2B). Although there is evidence for in vivo and in vitro toxicity, the mechanisms of cobalt-induced lung toxicity are not fully known. The purpose of this work was to identify potential signatures of acute cobalt exposure using a toxico-genomic approach. Data analysis focused on some cellular processes and protein targets that are thought to be relevant for carcinogenesis, transport and bio-marker research. Results: A time course transcriptome analysis was performed on A549 human pulmonary cells, leading to the identification of 85 genes which are repressed or induced in response to soluble 59 Co. A group of 29 of these genes, representing the main biological functions, was assessed by quantitative RT-PCR. The expression profiles of six of them were then tested by quantitative RT-PCR in a time-dependent manner and three modulations were confirmed by Western blotting. The 85 modulated genes include potential cobalt carriers (FBXL2, ZNT1, SLC12A5), tumor suppressors or transcription factors (MAZ, DLG1, MYC, AXL) and genes linked to the stress response (UBC, HSPCB, BN1P3L). We also identified nine genes coding for secreted proteins as candidates for bio-marker research. Of those, T1MP2 was found to be down-regulated and this modulation was confirmed, in a dose-dependent manner, at protein level in the supernatant of exposed cells. Conclusion: Most of these genes have never been described as related to cobalt stress and provide original hypotheses for further study of the effects of this metal ion on human lung epithelial cells. A putative bio-marker of cobalt toxicity was identified. (authors)

Deposition and properties of cobalt- and ruthenium-based ultra-thin films

Science.gov (United States)

Henderson, Lucas Benjamin

Future copper interconnect systems will require replacement of the materials that currently comprise both the liner layer(s) and the capping layer. Ruthenium has previously been considered as a material that could function as a single material liner, however its poor ability to prevent copper diffusion makes it incompatible with liner requirements. A recently described chemical vapor deposition route to amorphous ruthenium-phosphorus alloy films could correct this problem by eliminating the grain boundaries found in pure ruthenium films. Bias-temperature stressing of capacitor structures using 5 nm ruthenium-phosphorus film as a barrier to copper diffusion and analysis of the times-to-failure at accelerated temperature and field conditions implies that ruthenium-phosphorus performs acceptably as a diffusion barrier for temperatures above 165°C. The future problems associated with the copper capping layer are primarily due to the poor adhesion between copper and the current Si-based capping layers. Cobalt, which adheres well to copper, has been widely proposed to replace the Si-based materials, but its ability to prevent copper diffusion must be improved if it is to be successfully implemented in the interconnect. Using a dual-source chemistry of dicobaltoctacarbonyl and trimethylphosphine at temperatures from 250-350°C, amorphous cobalt-phosphorus can be deposited by chemical vapor deposition. The films contain elemental cobalt and phosphorus, plus some carbon impurity, which is incorporated in the film as both graphitic and carbidic (bonded to cobalt) carbon. When deposited on copper, the adhesion between the two materials remains strong despite the presence of phosphorus and carbon at the interface, but the selectivity for growth on copper compared to silicon dioxide is poor and must be improved prior to consideration for application in interconnect systems. A single molecule precursor containing both cobalt and phosphorus atoms, tetrakis(trimethylphosphine)cobalt

Model studies of secondary hydrogenation in Fischer-Tropsch synthesis studied by cobalt catalysts

Energy Technology Data Exchange (ETDEWEB)

Aaserud, Christian

2003-07-01

Mass transfer effects are very important in Fischer-Tropsch (FT) synthesis. In order to study the FT synthesis without the influence of any transport limitations, cobalt foils have been used as model catalysts. The effect of pretreatment (number of calcinations and different reduction times) for cobalt foil catalysts at 220 {sup o}C, 1 bar and H{sub 2}/CO = 3 has been studied in a microreactor. The foils were examined by Scanning electron microscopy (SEM). It was found that the catalytic activity of the cobalt foil increases with the number of pretreatments possibly due to an increase in the surface area of the cobalt foil. The SEM results support the assumption that the surface area of the cobalt foil increases with the number of pretreatments. The reduction time was also found to influence the catalytic activity of the cobalt foil. Highest activity was obtained using a reduction time of only five min (compared to one and thirty min). The decrease in activity after reduction for thirty min compared to five min was suggested to be due to restructuring of the surface of the cobalt foil and a reduction time of only 1 min was not enough to reduce the cobalt foil sufficiently. Time of reduction did also influence the product distribution. Increased reduction time resulted in a lower selectivity to light products and increased selectivity to heavier components. The paraffin/olefin ratio increased with increasing CO-conversion also for cobalt foils. The paraffin/olefin ratio also increased when the reduction period of the cobalt foil was increased at a given CO-conversion. Hydrogenation of propene to propane has been studied as a model reaction for secondary hydrogenation of olefins in the FT synthesis. The study has involved promoted and unpromoted cobalt FT catalysts supported on different types of supports and also unsupported cobalt. Hydrogenation of propene was carried out at 120 {sup o}C, 1.8 bar and H{sub 2}/C{sub 3}H{sub 6} 6 in a fixed bed microreactor. The rate

Bis(2-methoxybenzylammonium diaquabis(dihydrogen diphosphato-κ2O,O′cobaltate(II dihydrate

Directory of Open Access Journals (Sweden)

Adel Elboulali

2014-04-01

Full Text Available The title compound, (C8H12NO2[Co(H2P2O72(H2O2]·2H2O, crystallizes isotypically with its MnII analogue. It consists of alternating layers of organic cations and inorganic complex anions, extending parallel to (100. The complex cobaltate(II anion exhibits -1 symmetry. Its Co2+ atom has an octahedral coordination sphere, defined by two water molecules in apical positions and two H2P2O72− ligands in equatorial positions. The cohesion between inorganic and organic layers is accomplished by a set of O—H...O and N—H...O hydrogen bonds involving the organic cation, the inorganic anion and the remaining lattice water molecules.

Cobalt-Based Electrolytes for Dye-Sensitized Solar Cells: Recent Advances towards Stable Devices

Directory of Open Access Journals (Sweden)

Federico Bella

2016-05-01

Full Text Available Redox mediators based on cobalt complexes allowed dye-sensitized solar cells (DSCs to achieve efficiencies exceeding 14%, thus challenging the emerging class of perovskite solar cells. Unfortunately, cobalt-based electrolytes demonstrate much lower long-term stability trends if compared to the traditional iodide/triiodide redox couple. In view of the large-scale commercialization of cobalt-based DSCs, the scientific community has recently proposed various approaches and materials to increase the stability of these devices, which comprise gelling agents, crosslinked polymeric matrices and mixtures of solvents (including water. This review summarizes the most significant advances recently focused towards this direction, also suggesting some intriguing way to fabricate third-generation cobalt-based photoelectrochemical devices stable over time.

Sorption of cobalt and zinc from fresh water and seawater

International Nuclear Information System (INIS)

Arnoldus, R.; Weijden, C.H. van der; Das, H.A.

1977-01-01

The adsorption of Cosup(II) and Znsup(II) from artificial fresh and sea water on to clay minerals is studied. The adsorption isotherms are measured at pH-values of 7 and 8. The specific adsorption of zinc is higher than that of cobalt. This is compatible with the higher average residence time of cobalt than that of zinc in the oceans

Influence of Cobalt Doping on the Physical Properties of Zn0.9Cd0.1S Nanoparticles

Directory of Open Access Journals (Sweden)

Gupta Hari Om

2009-01-01

Full Text Available Abstract Zn0.9Cd0.1S nanoparticles doped with 0.005–0.24 M cobalt have been prepared by co-precipitation technique in ice bath at 280 K. For the cobalt concentration >0.18 M, XRD pattern shows unidentified phases along with Zn0.9Cd0.1S sphalerite phase. For low cobalt concentration (≤0.05 M particle size, d XRDis ~3.5 nm, while for high cobalt concentration (>0.05 M particle size decreases abruptly (~2 nm as detected by XRD. However, TEM analysis shows the similar particle size (~3.5 nm irrespective of the cobalt concentration. Local strain in the alloyed nanoparticles with cobalt concentration of 0.18 M increases ~46% in comparison to that of 0.05 M. Direct to indirect energy band-gap transition is obtained when cobalt concentration goes beyond 0.05 M. A red shift in energy band gap is also observed for both the cases. Nanoparticles with low cobalt concentrations were found to have paramagnetic nature with no antiferromagnetic coupling. A negative Curie–Weiss temperature of −75 K with antiferromagnetic coupling was obtained for the high cobalt concentration.

Synthesis, Structures and Properties of Cobalt Thiocyanate Coordination Compounds with 4-(hydroxymethylpyridine as Co-ligand

Directory of Open Access Journals (Sweden)

Stefan Suckert

2016-04-01

Full Text Available Reaction of Co(NCS2 with 4-(hydroxymethylpyridine (hmpy leads to the formation of six new coordination compounds with the composition [Co(NCS2(hmpy4] (1, [Co(NCS2(hmpy4] × H2O (1-H2O, [Co(NCS2(hmpy2(EtOH2] (2, [Co(NCS2(hmpy2(H2O2] (3, [Co(NCS2(hmpy2]n∙4 H2O (4 and [Co(NCS2(hmpy2]n (5. They were characterized by single crystal and powder X-ray diffraction experiments, thermal and elemental analysis, IR and magnetic measurements. Compound 1 and 1-H2O form discrete complexes, in which the Co(II cations are octahedrally coordinated by two terminal thiocyanato anions and four 4-(hydroxymethylpyridine ligands. Discrete complexes were also observed for compounds 2 and 3 where two of the hmpy ligands were substituted by solvent, either water (3 or ethanol (2. In contrast, in compounds 4 and 5, the Co(II cations are linked into chains by bridging 4-(hydroxymethylpyridine ligands. The phase purity was checked with X-ray powder diffraction. Thermogravimetric measurements showed that compound 3 transforms into 5 upon heating, whereas the back transformation occurs upon resolvation. Magnetic measurements did not show any magnetic exchange via the hmpy ligand for compound 5.

Selected aspects of the action of cobalt ions in the human body.

Science.gov (United States)

Czarnek, Katarzyna; Terpiłowska, Sylwia; Siwicki, Andrzej K

2015-01-01

Cobalt is widespread in the natural environment and can be formed as an effect of anthropogenic activity. This element is used in numerous industrial applications and nuclear power plants. Cobalt is an essential trace element for the human body and can occur in organic and inorganic forms. The organic form is a necessary component of vitamin B12 and plays a very important role in forming amino acids and some proteins in nerve cells, and in creating neurotransmitters that are indispensable for correct functioning of the organism. Its excess or deficiency will influence it unfavourably. Salts of cobalt have been applied in medicine in the treatment of anaemia, as well as in sport as an attractive alternative to traditional blood doping. Inorganic forms of cobalt present in ion form, are toxic to the human body, and the longer they are stored in the body, the more changes they cause in cells. Cobalt gets into the body in several ways: firstly, with food; secondly by the respiratory system; thirdly, by the skin; and finally, as a component of biomaterials. Cobalt and its alloys are fundamental components in orthopaedic implants and have been used for about 40 years. The corrosion of metal is the main problem in the construction of implants. These released metal ions may cause type IV inflammatory and hypersensitivity reactions, and alternations in bone modelling that lead to aseptic loosening and implant failure. The ions of cobalt released from the surface of the implant are absorbed by present macrophages, which are involved in many of the processes associated with phagocytose orthopaedic biomaterials particles and release pro-inflammatory mediators such as interleukin-1 (IL-1), interleukin-6 (IL-6), tumour necrosis factor α (TNF-α), and prostaglandin.

Preliminary feasibility study on production of cobalt-60 source for industrial irradiation

International Nuclear Information System (INIS)

Joo, Po Kook; Park, Kyung Bae; Ahn, Yun Soo; Lee, Jong Tai; Kim, Hark Rho

1999-05-01

As there is a high possible demand of industrial Co-60 source in the world market, feasibility study of a project was performed to produce and to export Co-60 sources, utilizing KEPCO's Wolsung NPP for irradiation of cobalt and KAERI's hot-cells for fabrication of cobalt sources. Main concerns of the study were to understand irradiation and fabrication (encapsulation) processes and to examine related technologies, required facilities and equipment. In particular, it was examined intensively if it would be possible to modify facilities around the reactor vessel of Wolsung NPP tp substantiate the related licensing in order to irradiate cobalt in the reactor. It is expected that once, if cooperation scheme with MDS Nordion of Canada is established, main issues such as modification of facilities, related licensing, raw material procurement and technology transfer for high quality product will be solved. In order to review overall feasibility of the project, present status and prospect of the world market was surveyed and various usages of cobalt sources were reviewed with emphasis on possible demand increase per usage. Food poisoning accidents are prevailing worldwide and food irradiation with cobalt sources is considered as a promising measure to prevent them and may bring forth high increase of cobalt sources demand in the world market. Preliminary economic feasibility was studied in conservation, evaluating roughly the investment and the operating cost based on materials from various information sources. (author)

Fabrication and analysis of ordered magnetic cobalt nanoparticles; Herstellung und Untersuchung geordneter magnetischer Kobaltnanoteilchen

Energy Technology Data Exchange (ETDEWEB)

Zuern, Klaus P.

2009-12-17

In the dissertation on hand monodisperse, wellordered magnetic cobalt and cobalt hydride nanoparticles have been produced and investigated magnetically. The preparation was achieved by diblock-copolymer-micelles filled with cobalt salt, from which nanoparticles of elementary cobalt respectively cobalt hydride were generated in different steps of the procedure. It was evident that the cobalthydride generated by the hydrogen plasma was surprisingly stable. It could even be taken into consideration as a hydrogen storage device for fuel cell. The magnetic properties of the particles has been investigated by x-ray magnetic circular dichroism (XMCD). In addition it was evident, that it was principally impossible to investigate a film layered on a substrate with a SQUID-magnetometer, if this film produces only a small signal as well absolutely as relatively to the magnetically measured total moment of the sample. (orig.)

Recovery of cobalt and lithium fromspent Li-ion batteries

OpenAIRE

Busnardo, Natália Giovanini; Paulino, Jéssica Frontino; Afonso, Julio Carlos

2007-01-01

The "active mass" (cathode + anode + electrolyte) of spent Li-ion batteries was submitted to one of the following procedures: (a) it was calcined (500 ºC) and submitted to extraction with water to recover lithium salts. The residual solid was treated with sulfuric acid containing hydrogen peroxide. Cobalt was recovered as sulfate; (b) the "active mass" was treated with potassium hydrogen sulfate (500 ºC) and dissolved in water. Cobalt was precipitated together with copper after addition of so...

Enhanced magnetocrystalline anisotropy in deposited cobalt clusters

Energy Technology Data Exchange (ETDEWEB)

Eastham, D.A.; Denby, P.M.; Kirkman, I.W. [Daresbury Laboratory, Daresbury, Warrington (United Kingdom); Harrison, A.; Whittaker, A.G. [Department of Chemistry, University of Edinburgh, Edinburgh (United Kingdom)

2002-01-28

The magnetic properties of nanomaterials made by embedding cobalt nanocrystals in a copper matrix have been studied using a SQUID magnetometer. The remanent magnetization at temperatures down to 1.8 K and the RT (room temperature) field-dependent magnetization of 1000- and 8000-atom (average-size) cobalt cluster samples have been measured. In all cases it has been possible to relate the morphology of the material to the magnetic properties. However, it is found that the deposited cluster samples contain a majority of sintered clusters even at cobalt concentrations as low as 5% by volume. The remanent magnetization of the 8000-atom samples was found to be bimodal, consisting of one contribution from spherical particles and one from touching (sintered) clusters. Using a Monte Carlo calculation to simulate the sintering it has been possible to calculate a size distribution which fits the RT superparamagnetic behaviour of the 1000-atom samples. The remanent magnetization for this average size of clusters could then be fitted to a simple model assuming that all the nanoparticles are spherical and have a size distribution which fits the superparamagnetic behaviour. This gives a value for the potential energy barrier height (for reversing the spin direction) of 2.0 {mu}eV/atom which is almost four times the accepted value for face-centred-cubic bulk cobalt. The remanent magnetization for the spherical component of the large-cluster sample could not be fitted with a single barrier height and it is conjectured that this is because the barriers change as a function of cluster size. The average value is 1.5 {mu}eV/atom but presumably this value tends toward the bulk value (0.5 {mu}eV/atom) for the largest clusters in this sample. (author)

Tungsen--nickel--cobalt alloy and method of producing same

International Nuclear Information System (INIS)

Dickinson, J.M.; Riley, R.E.

1977-01-01

An improved tungsten alloy having a tungsten content of approximately 95 weight percent, a nickel content of about 3 weight percent, and the balance being cobalt of about 2 weight percent is described. A method for producing this tungsten--nickel--cobalt alloy is further described and comprises coating the tungsten particles with a nickel--cobalt alloy, pressing the coated particles into a compact shape, heating the compact in hydrogen to a temperature in the range of 1400 0 C and holding at this elevated temperature for a period of about 2 hours, increasing this elevated temperature to about 1500 0 C and holding for 1 hour at this temperature, cooling to about 1200 0 C and replacing the hydrogen atmosphere with an inert argon atmosphere while maintaining this elevated temperature for a period of about 1 / 2 hour, and cooling the resulting alloy to room temperature in this argon atmosphere

Molecular dynamics simulation of thermophysical properties of undercooled liquid cobalt

International Nuclear Information System (INIS)

Han, X J; Wang, J Z; Chen, M; Guo, Z Y

2004-01-01

Molecular dynamics simulations with two different embedded-atom-method (EAM) potentials are applied to calculate the density, specific heat and self-diffusion coefficient of liquid cobalt at temperatures above and below the melting temperature. Simulation shows that Pasianot's EAM model of cobalt constructed on the basis of a hcp structure is more successful than Stoop's EAM model in the framework of a fcc structure in predicting the thermophysical properties of liquid cobalt. Simulations with Pasianot's EAM model indicate that the density fits into ρ = 7.49-9.17 x 10 -4 (T- T m ) g cm -3 , and the self-diffusion coefficient is given by D = 1.291 x 10 -7 exp(-48 795.71/RT) m 2 s -1 . Dissimilar to the linear dependence of the density and the Arrhenius dependence of the self-diffusion coefficient on temperature, the specific heat shows almost a constant value of 38.595 ± 0.084 J mol -1 K -1 within the temperature range of simulation. The simulated properties of liquid cobalt are compared with experimental data available. Comparisons show reasonable agreements between the simulated results from Pasianot's EAM model and experimental data

Electrochemically deposited hybrid nickel-cobalt hexacyanoferrate nanostructures for electrochemical supercapacitors

International Nuclear Information System (INIS)

Safavi, A.; Kazemi, S.H.; Kazemi, H.

2011-01-01

Highlights: → Nanostructured hybrid nickel-cobalt hexacyanoferrate is used in supercapacitors. → A high capacitance (765 F g -1 ) is obtained at a specific current of 0.2 A g -1 . → Long cycle-life and excellent stability are demonstrated during 1000 cycles. - Abstract: This study describes the use of electrodeposited nanostructured hybrid nickel-cobalt hexacyanoferrate in electrochemical supercapacitors. Herein, various compositions of nickel and cobalt hexacyanoferrates (Ni/CoHCNFe) nanostructures are electrodeposited on an inexpensive stainless steel substrate using cyclic voltammetric (CV) method. The morphology of the electrodeposited nanostructures is studied using scanning electron microscopy, while their electrochemical characterizations are investigated using CV, galvanostatic charge and discharge and electrochemical impedance spectroscopy. The results show that the nanostructures of hybrid metal cyanoferrate, shows a much higher capacitance (765 F g -1 ) than those obtained with just nickel hexacyanoferrate (379 F g -1 ) or cobalt hexacyanoferrate (277 F g -1 ). Electrochemical impedance spectroscopy results confirm the favorable capacitive behavior of the electrodeposited materials. The columbic efficiency is approximately 95% based on the charge and discharge experiments. Long cycle-life and excellent stability of the nanostructured materials are also demonstrated during 1000 cycles.

Electrochemically deposited hybrid nickel-cobalt hexacyanoferrate nanostructures for electrochemical supercapacitors

Energy Technology Data Exchange (ETDEWEB)

Safavi, A., E-mail: safavi@chem.susc.ac.ir [Department of Chemistry, College of Sciences, Shiraz University, Shiraz 71454 (Iran, Islamic Republic of); Nanotechnology Research Institute, Shiraz University, Shiraz (Iran, Islamic Republic of); Kazemi, S.H., E-mail: habibkazemi@iasbs.ac.ir [Department of Chemistry, Institute for Advanced Studies in Basic Sciences (IASBS), Zanjan 45137-66731 (Iran, Islamic Republic of); Kazemi, H. [Department of Chemistry, College of Sciences, Shiraz University, Shiraz 71454 (Iran, Islamic Republic of)

2011-10-30

Highlights: > Nanostructured hybrid nickel-cobalt hexacyanoferrate is used in supercapacitors. > A high capacitance (765 F g{sup -1}) is obtained at a specific current of 0.2 A g{sup -1}. > Long cycle-life and excellent stability are demonstrated during 1000 cycles. - Abstract: This study describes the use of electrodeposited nanostructured hybrid nickel-cobalt hexacyanoferrate in electrochemical supercapacitors. Herein, various compositions of nickel and cobalt hexacyanoferrates (Ni/CoHCNFe) nanostructures are electrodeposited on an inexpensive stainless steel substrate using cyclic voltammetric (CV) method. The morphology of the electrodeposited nanostructures is studied using scanning electron microscopy, while their electrochemical characterizations are investigated using CV, galvanostatic charge and discharge and electrochemical impedance spectroscopy. The results show that the nanostructures of hybrid metal cyanoferrate, shows a much higher capacitance (765 F g{sup -1}) than those obtained with just nickel hexacyanoferrate (379 F g{sup -1}) or cobalt hexacyanoferrate (277 F g{sup -1}). Electrochemical impedance spectroscopy results confirm the favorable capacitive behavior of the electrodeposited materials. The columbic efficiency is approximately 95% based on the charge and discharge experiments. Long cycle-life and excellent stability of the nanostructured materials are also demonstrated during 1000 cycles.

New efficient catalyst for ammonia synthesis: barium-promoted cobalt on carbon

DEFF Research Database (Denmark)

Hagen, Stefan; Barfod, Rasmus; Fehrmann, Rasmus

2002-01-01

Barium-promoted cobalt catalysts supported on carbon exhibit higher ammonia activities at synthesis temperatures than the commercial, multipromoted iron catalyst and also a lower ammonia......Barium-promoted cobalt catalysts supported on carbon exhibit higher ammonia activities at synthesis temperatures than the commercial, multipromoted iron catalyst and also a lower ammonia...

Evidence of spin transition and charge order in cobalt substituted La sub 0 sub . sub 7 Ca sub 0 sub . sub 3 MnO sub 3

CERN Document Server

Srivastava, C M; Gundurao, T K; Nigam, A K; Bahadur, D

2003-01-01

The transport and magnetic studies of a series of compounds having the general formula La sub 0 sub . sub 7 Ca sub 0 sub . sub 3 Mn sub 1 sub - sub x Co sub x O sub 3 (0.1 = 0.25 there is a clear spin transition at low temperature from the high to the low spin state of trivalent cobalt and this leads to change in ferromagnetic (FM) and antiferromagnetic (AFM) phases. For x >= 0.25 there are two transitions for each value of x: the upper one gives the FM and AFM spin arrangement depending upon whether the DE or the SE dominates; the lower one is obtained due to the transition from the high to the low spin state of the trivalent cobalt ion.

Construction of Pyrrolo[1,2-a]indoles via Cobalt(III)-Catalyzed Enaminylation of 1-(Pyrimidin-2-yl)-1H-indoles with Ketenimines and Subsequent Base-Promoted Cyclization.

Science.gov (United States)

Zhou, Xiaorong; Fan, Zili; Zhang, Zhiyin; Lu, Ping; Wang, Yanguang

2016-09-16

A cobalt(III)-catalyzed cross-coupling reaction of 1-(pyrimidin-2-yl)-1H-indoles with ketenimines is reported. The reaction provided 2-enaminylated indole derivatives in moderate to excellent yields with a broad substrate scope. The prepared 2-enaminylated indoles could be conveniently converted into pyrrolo[1,2-a]indoles, which are an important class of compounds in medicinal chemistry.

Distribution of cobalt in soil from Kavadarci and the environs

International Nuclear Information System (INIS)

Stafilov, Trajche; Shajn, Robert; Boev, Blazho; Cvetkovich, Julujana; Mukaetov, Dushko; Andreevski, Marjan; Lepitkova, Sonja

2009-01-01

The results of the study of spatial distribution of cobalt in surface soil and subsoil over of the Kavadarci region, Republic of Macedonia, are reported. From the investigated region (360 km 2 ) in total 344 soil samples from 172 locations were collected. At each sampling point soil samples were collected at two depths, topsoil (0-5 cm) and subsoil soil (20-30 cm). Inductively coupled plasma - mass spectrometry (ICP-MS) was applied for the determination of cobalt. Data analysis and construction of the map were performed using the Paradox (ver. 9), Statistica (ver. 6.1), AutoDesk Map (ver. 2008) and Surfer (ver. 8.09) software. It was found that for both topsoil and subsoil the median and average values are 15 mg/kg, ranges between 6.7 and 58 mg/kg. The highest content of cobalt is present in the soil from the area of Paleozoic and Mesozoic rocks (Pz-Mz) on the western part of the investigated area and Flysch (E) - Eocene upper flysch zone (on the northern part) and the lowest in the soils from the Holocene alluvium of the rivers Crna Reka and Vardar. There are no significant differences between the surface and subsoil in terms of its average quantities. It was found that the critically high contents are related primarily to high contents of cobalt in the sampling points from the western part of the investigated region. The contents of cobalt are higher in subsoil than in topsoil from which it can be concluded that the occurrence is natural.

Effect of rare earth substitution in cobalt ferrite bulk materials

International Nuclear Information System (INIS)

Bulai, G.; Diamandescu, L.; Dumitru, I.; Gurlui, S.; Feder, M.; Caltun, O.F.

2015-01-01

The study was focused on the influence of small amounts of rare earth (RE=La, Ce, Sm, Gd, Dy, Ho, Er, Yb) addition on the microstructure, phase content and magnetic properties of cobalt ferrite bulk materials. The X-Ray diffraction measurements confirmed the formation of the spinel structure but also the presence of secondary phases of RE oxides or orthoferrite in small percentages (up to 3%). Density measurements obtained by Archimedes method revealed a ~1 g cm −3 decrease for the RE doped cobalt ferrite samples compared with stoichiometric one. Both the Mössbauer and Fourier Transform Infrared Spectrocopy analysis results confirmed the formation of the spinel phase. The saturation magnetization and coercive field values of the doped samples obtained by Vibrating Sample Magnetometry were close to those of the pure cobalt ferrite. For magnetostrictive property studies the samples were analyzed using the strain gauge method. Higher maximum magnetostriction coefficients were found for the Ho, Ce, Sm and Yb doped cobalt ferrite bulk materials as related to the stoichiometric CoFe 2 O 4 sample. Moreover, improved strain derivative was observed for these samples but at higher magnetic fields due to the low increase of the coercive field values for doped samples. - Highlights: • Substitution by a large number of rare earth elements was investigated. • First reported results on magnetostriction measurements of RE doped cobalt ferrite. • The doped samples presented an increased porosity and a decreased grain size. • Increased magnetostrctive response was observed for several doped samples

Enhancement of electrical conductivity in gamma irradiated cobalt ferrite nanoparticles

International Nuclear Information System (INIS)

Nawpute, Asha A.; Raut, A.V.; Babrekar, M.K.; Kale, C.M.; Jadhav, K.M.; Shinde, A.B.

2014-01-01

The cobalt ferrite nanoparticles were synthesized by sol-gel auto- combustion method, in which L-ascorbic acid was used as a fuel. The effect of gamma irradiation on the electrical resistivity of cobalt ferrite nanoparticles has been studied. The ferrite powder annealed at 550℃ was irradiated by gamma source 137 Cs. The synthesized nanoparticles were characterized by X-ray diffraction and DC resistivity. (author)

Coordination compounds of cobalt(II), nickel(II), copper(II), and zinc(II) with pantothenic acid

Energy Technology Data Exchange (ETDEWEB)

Shabilalov, A.A.; Yunuskhodzhaev, A.N.; Khodzhaev, O.F.; Azizov, M.A.

1986-11-01

The compounds Ni(PANA - H)/sub 2/ x 4H/sub 2/O (PANA stands for pantothenic acid, and - H indicates a deprotonated ligand), Cu(PANA - H)/sub 2/ x 2H/sub 2/O, Zn(PANA - H)/sub 2/ x H/sub 2/O, Co(PANA - H)Cl x H/sub 2/O, and Ni(PANA - H)Cl x 3H/sub 2/O have been synthesized on the basis of pantothenic acid and Co(II), Ni(II), Cu(II), and Zn(II) salts in aqueous media. The compounds have been identified by elemental and x-ray diffraction analysis. Some physicochemical properties (solubility, melting point, molar conductivity) of the compounds obtained have been studied. The structure of the compounds isolated has been established on the basis of an analysis of their IR, ESR, and electronic spectra, as well as derivatograms.

Uptake of radionuclides caesium and cobalt

International Nuclear Information System (INIS)

Lukac, P.; Foldesova, M.

1995-01-01

By means of chemical treatment ammonium, potassium, sodium and H-form of zeolite were prepared. The chemical modifications of zeolite were carried out with: 2M solution of NaNO 3 , NH 4 NO 3 , KNO 3 ; 0,1M solution of HCl; NaOH solution of different concentration. The method of model radioactive solution was used to find the sorption ability for cesium and cobalt every modified zeolite. The model solution were 0.05M solution of cobalt labelled by 60 Co or cesium labelled by 137 Cs. The highest sorption ability was observed for zeolite modified by NaOH. The influence of pH on uptake of cesium and cobalt by modified zeolite was searched as well. The experimental data (leaching tests, compressive strength measurement and porosity) were measured for the case the Cs and Cs from model water solution and radioactive waste water were up taken on chemically modified zeolite and were subsequently incorporated into cement casts on blast furnace cement slags basis. The leachability was tested in water, in basis solution and in acid solution. The leachability in water and basic solution was negligible, in acid solution it was less than 4% which is inside of value of applied measure method. The compressive strength, porosity and leaching experiment are hopefully and show good mechanical stability and good retention of observed radionuclides in samples exposed in leaching solutions. (J.K.)

Cobalt ferrite nanoparticles under high pressure

Energy Technology Data Exchange (ETDEWEB)

Saccone, F. D.; Ferrari, S.; Grinblat, F.; Bilovol, V. [Instituto de Tecnologías y Ciencias de la Ingeniería, “Ing. H. Fernández Long,” Av. Paseo Colón 850 (1063), Buenos Aires (Argentina); Errandonea, D., E-mail: daniel.errandonea@uv.es [Departamento de Fisica Aplicada, Institut Universitari de Ciència dels Materials, Universitat de Valencia, c/ Doctor Moliner 50, E-46100 Burjassot, Valencia (Spain); Agouram, S. [Departamento de Física Aplicada y Electromagnetismo, Universitat de València, 46100 Burjassot, Valencia (Spain)

2015-08-21

We report by the first time a high pressure X-ray diffraction and Raman spectroscopy study of cobalt ferrite (CoFe{sub 2}O{sub 4}) nanoparticles carried out at room temperature up to 17 GPa. In contrast with previous studies of nanoparticles, which proposed the transition pressure to be reduced from 20–27 GPa to 7.5–12.5 GPa (depending on particle size), we found that cobalt ferrite nanoparticles remain in the spinel structure up to the highest pressure covered by our experiments. In addition, we report the pressure dependence of the unit-cell parameter and Raman modes of the studied sample. We found that under quasi-hydrostatic conditions, the bulk modulus of the nanoparticles (B{sub 0} = 204 GPa) is considerably larger than the value previously reported for bulk CoFe{sub 2}O{sub 4} (B{sub 0} = 172 GPa). In addition, when the pressure medium becomes non-hydrostatic and deviatoric stresses affect the experiments, there is a noticeable decrease of the compressibility of the studied sample (B{sub 0} = 284 GPa). After decompression, the cobalt ferrite lattice parameter does not revert to its initial value, evidencing a unit cell contraction after pressure was removed. Finally, Raman spectroscopy provides information on the pressure dependence of all Raman-active modes and evidences that cation inversion is enhanced by pressure under non-hydrostatic conditions, being this effect not fully reversible.

Uptake of radionuclides caesium and cobalt

Energy Technology Data Exchange (ETDEWEB)

Lukac, P; Foldesova, M [Slovak Technical Univ., Bratislava (Slovakia)

1996-12-31

By means of chemical treatment ammonium, potassium, sodium and H-form of zeolite were prepared. The chemical modifications of zeolite were carried out with: 2M solution of NaNO{sub 3}, NH{sub 4}NO{sub 3}, KNO{sub 3}; 0,1M solution of HCl; NaOH solution of different concentration. The method of model radioactive solution was used to find the sorption ability for cesium and cobalt every modified zeolite. The model solution were 0.05M solution of cobalt labelled by {sup 60}Co or cesium labelled by {sup 137}Cs. The highest sorption ability was observed for zeolite modified by NaOH. The influence of pH on uptake of cesium and cobalt by modified zeolite was searched as well. The experimental data (leaching tests, compressive strength measurement and porosity) were measured for the case the Cs and Cs from model water solution and radioactive waste water were up taken on chemically modified zeolite and were subsequently incorporated into cement casts on blast furnace cement slags basis. The leachability was tested in water, in basis solution and in acid solution. The leachability in water and basic solution was negligible, in acid solution it was less than 4% which is inside of value of applied measure method. The compressive strength, porosity and leaching experiment are hopefully and show good mechanical stability and good retention of observed radionuclides in samples exposed in leaching solutions. (J.K.).

Cobalt doped antimony oxide nano-particles based chemical sensor and photo-catalyst for environmental pollutants

Energy Technology Data Exchange (ETDEWEB)

Jamal, Aslam [Centre for Advanced Materials and Nano-Engineering (CAMNE) and Department of Chemistry, Faculty of Sciences and Arts, Najran University, P. O. Box 1988, Najran 11001 (Saudi Arabia); Rahman, Mohammed M. [Center of Excellence for Advanced Materials Research (CEAMR), King Abdulaziz University, P.O. Box 80203, Jeddah 21589 (Saudi Arabia); Chemistry Department, Faculty of Science, King Abdulaziz University, P.O. Box 80203, Jeddah 21589 (Saudi Arabia); Khan, Sher Bahadar, E-mail: drkhanmarwat@gmail.com [Center of Excellence for Advanced Materials Research (CEAMR), King Abdulaziz University, P.O. Box 80203, Jeddah 21589 (Saudi Arabia); Chemistry Department, Faculty of Science, King Abdulaziz University, P.O. Box 80203, Jeddah 21589 (Saudi Arabia); Faisal, Mohd. [Centre for Advanced Materials and Nano-Engineering (CAMNE) and Department of Chemistry, Faculty of Sciences and Arts, Najran University, P. O. Box 1988, Najran 11001 (Saudi Arabia); Akhtar, Kalsoom [Division of Nano Sciences and Department of Chemistry, Ewha Womans University, Seoul 120-750 (Korea, Republic of); Rub, Malik Abdul; Asiri, Abdullah M.; Al-Youbi, Abdulrahman O. [Center of Excellence for Advanced Materials Research (CEAMR), King Abdulaziz University, P.O. Box 80203, Jeddah 21589 (Saudi Arabia); Chemistry Department, Faculty of Science, King Abdulaziz University, P.O. Box 80203, Jeddah 21589 (Saudi Arabia)

2012-11-15

Graphical abstract: A dichloromethane chemical sensor using cobalt antimony oxides has been fabricated. This sensor showed high sensitivity and will be a useful candidate for environmental and health monitoring. Also it showed high photo-catalytic activity and can be a good candidate as a photo-catalyst for organic hazardous materials. Highlights: Black-Right-Pointing-Pointer Reusable chemical sensor. Black-Right-Pointing-Pointer Green environmental and eco-friendly chemi-sensor. Black-Right-Pointing-Pointer High sensitivity. Black-Right-Pointing-Pointer Good candidate for environmental and health monitoring. - Abstract: Cobalt doped antimony oxide nano-particles (NPs) have been synthesized by hydrothermal process and structurally characterized by utilizing X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM) and Fourier transforms infrared spectrophotometer (FT-IR) which revealed that the synthesized cobalt antimony oxides (CoSb{sub 2}O{sub 6}) are well crystalline nano-particles with an average particles size of 26 {+-} 10 nm. UV-visible absorption spectra ({approx}286 nm) were used to investigate the optical properties of CoSb{sub 2}O{sub 6}. The chemical sensing of CoSb{sub 2}O{sub 6} NPs have been primarily investigated by I-V technique, where dichloromethane is used as a model compound. The analytical performance of dichloromethane chemical sensor exhibits high sensitivity (1.2432 {mu}A cm{sup -2} mM{sup -1}) and a large linear dynamic range (1.0 {mu}M-0.01 M) in short response time (10 s). The photo catalytic activity of the synthesized CoSb{sub 2}O{sub 6} nano-particles was evaluated by degradation of acridine orange (AO), which degraded 58.37% in 200 min. These results indicate that CoSb{sub 2}O{sub 6} nano-particles can play an excellent research impact in the environmental field.

Health physics monitoring during cobalt slug rod handling at research reactor Dhruva: an experience

International Nuclear Information System (INIS)

Verma, Gopal P.; Bhatnagar, Amit; Krishnamohanan, T.; Kalyanasundaram, N.; Gupta, P.C.; Pushparaja; Ghosh, Runner

2006-01-01

Cobalt-60 is used in many industrial and medical applications, such as leveling devices, thickness gauge, sterilization of foodstuff to increase their shelf life, sterilization of medicines and in radiotherapy. The Cobalt slug rod containing cobalt pencils were irradiated for nearly two and half years in the Dhruva reactor core to obtain the 60 Co isotope. It had seen a total irradiation of 29053 MWD and the estimated total activity was 93.321 KCi. Campaign for the removal of irradiated rod from reactor core and retrieval of 60 Co pencils were carried out successfully in Dhruva Reactor complex. In view of such a high activity handled, the job was carried out after exhaustive prior planning and according to approved checklists. Radiation Hazards Control Unit, Dhruva provided Radiation Safety surveillance during the entire handling operation consisting of retrieval of the cobalt pencils and disposal of the aluminum slugs used to house the cobalt pencils in the Cobalt slug rod assembly. The whole operation was carried out in such a safe manner that the total man-rem consumption was insignificant. The operational radiation protection methods followed and the experience gained during the campaign are discussed in this paper. (author)

The influence of manganese–cobalt oxide/graphene on reducing fire hazards of poly(butylene terephthalate)

Energy Technology Data Exchange (ETDEWEB)

Wang, Dong; Zhang, Qiangjun; Zhou, Keqing; Yang, Wei [State Key Laboratory of Fire Science, University of Science and Technology of China, 96 Jinzhai Road, Hefei, Anhui 230026 (China); Hu, Yuan, E-mail: yuanhu@ustc.edu.cn [State Key Laboratory of Fire Science, University of Science and Technology of China, 96 Jinzhai Road, Hefei, Anhui 230026 (China); USTC-CityU Joint Advanced Research Centre, Suzhou Key Laboratory of Urban Public Safety, Suzhou Institute for Advanced Study, University of Science and Technology of China, 166 Ren’ai Road, Suzhou, Jiangsu 215123 (China); Gong, Xinglong, E-mail: gongxl@ustc.edu.cn [State Key Laboratory of Fire Science, University of Science and Technology of China, 96 Jinzhai Road, Hefei, Anhui 230026 (China); CAS Key Laboratory of Mechanical Behaviour and Design of Materials, Department of Modern Mechanics, University of Science and Technology of China, Hefei, Anhui 230026 (China)

2014-08-15

Highlights: • MnCo{sub 2}O{sub 4}–GNS hybrids are synthesized by a two-stage liquid phase method. • MnCo{sub 2}O{sub 4}–GNS/PBT composites were prepared via a masterbatch-melt blending method. • Fire hazards are monitored and evaluated by cone calorimeter and TG-IR. • MnCo{sub 2}O{sub 4}–GNS hybrids decrease thermal hazards and smoke hazards of PBT composites. • MnCo{sub 2}O{sub 4}–GNS hybrids perform better catalytic oxidation of CO and organic volatile. - Abstract: By means of direct nucleation and growth on the surface of graphene and element doping of cobalt oxide (Co{sub 3}O{sub 4}) nano-particles, manganese–cobalt oxide/graphene hybrids (MnCo{sub 2}O{sub 4}–GNS) were synthesized to reduce fire hazards of poly(butylene terephthalate) (PBT). The structure, elemental composition and morphology of the obtained hybrids were surveyed by X-ray diffraction, X-ray photoelectron spectrometer and transmission electron microscopy, respectively. Thermogravimetric analysis was applied to simulate and study the influence of MnCo{sub 2}O{sub 4}–GNS hybrids on thermal degradation of PBT during combustion. The fire hazards of PBT and its composites were assessed by the cone calorimeter. The cone test results had showed that peak HRR and SPR values of MnCo{sub 2}O{sub 4}–GNS/PBT composites were lower than that of pure PBT and Co{sub 3}O{sub 4}–GNS/PBT composites. Furthermore, the incorporation of MnCo{sub 2}O{sub 4}–GNS hybrids gave rise to apparent decrease of pyrolysis products containing aromatic compounds, carbonyl compounds, carbon monoxide and carbon dioxide, attributed to combined impact of physical barrier for graphene and cat O{sub 4} for organic volatiles and carbon monoxide.

Specific heat of rare earth cobaltates RCoO{sub 3} (R = La, Pr and Nd)

Energy Technology Data Exchange (ETDEWEB)

Thakur, Rasna, E-mail: rasnathakur@yahoo.com [Department of Physics, Barkatullah University, Bhopal 462026 (India); Srivastava, Archana [Department of Physics, Sri Sathya Sai College for Women, Bhopal 462024 (India); Thakur, Rajesh K.; Gaur, N.K. [Department of Physics, Barkatullah University, Bhopal 462026 (India)

2012-03-05

Highlights: Black-Right-Pointing-Pointer We have reported the temperature dependence (5 K {<=} T {<=} 1000 K) of the lattice contribution to the specific heat of rhombohedral LaCoO{sub 3} and orthocobaltates RCoO{sub 3} (R = Pr and Nd). Black-Right-Pointing-Pointer The strong electron phonon interactions are present in these compounds and lattice distortions can affect them substantially. Black-Right-Pointing-Pointer Thus Rigid Ion Model (RIM) is used for the first time to study the cohesive and thermal properties of the cobaltates RCoO{sub 3} with rare earth cation (R = La, Pr and Nd). Black-Right-Pointing-Pointer The values of specific heat calculated by us have shown remarkably good agreement with corresponding experimental data. Black-Right-Pointing-Pointer In addition, the results on the temperature dependence of cohesive energy ({phi}), molecular force constant (f), Reststrahlen frequency ({upsilon}), Debye temperature ({theta}{sub D}) and Gruneisen parameter ({gamma}) are also reported. - Abstract: We have reported the temperature dependence (5 K {<=} T {<=} 1000 K) of the lattice contribution to the specific heat of rhombohedral LaCoO{sub 3} and orthocobaltates RCoO{sub 3} (R = Pr and Nd). The strong electron phonon interactions are present in these compounds and lattice distortions can affect them substantially. Thus Rigid Ion Model (RIM) is used for the first time to study the cohesive and thermal properties of the cobaltates RCoO{sub 3} with rare earth cation (R = La, Pr and Nd). The values of specific heat calculated by us have shown remarkably good agreement with corresponding experimental data. In addition, the results on the temperature dependence of cohesive energy ({phi}), molecular force constant (f), Reststrahlen frequency ({upsilon}), Debye temperature ({theta}{sub D}) and Gruneisen parameter ({gamma}) are also reported.

The influence of manganese–cobalt oxide/graphene on reducing fire hazards of poly(butylene terephthalate)

International Nuclear Information System (INIS)

Wang, Dong; Zhang, Qiangjun; Zhou, Keqing; Yang, Wei; Hu, Yuan; Gong, Xinglong

2014-01-01

Highlights: • MnCo 2 O 4 –GNS hybrids are synthesized by a two-stage liquid phase method. • MnCo 2 O 4 –GNS/PBT composites were prepared via a masterbatch-melt blending method. • Fire hazards are monitored and evaluated by cone calorimeter and TG-IR. • MnCo 2 O 4 –GNS hybrids decrease thermal hazards and smoke hazards of PBT composites. • MnCo 2 O 4 –GNS hybrids perform better catalytic oxidation of CO and organic volatile. - Abstract: By means of direct nucleation and growth on the surface of graphene and element doping of cobalt oxide (Co 3 O 4 ) nano-particles, manganese–cobalt oxide/graphene hybrids (MnCo 2 O 4 –GNS) were synthesized to reduce fire hazards of poly(butylene terephthalate) (PBT). The structure, elemental composition and morphology of the obtained hybrids were surveyed by X-ray diffraction, X-ray photoelectron spectrometer and transmission electron microscopy, respectively. Thermogravimetric analysis was applied to simulate and study the influence of MnCo 2 O 4 –GNS hybrids on thermal degradation of PBT during combustion. The fire hazards of PBT and its composites were assessed by the cone calorimeter. The cone test results had showed that peak HRR and SPR values of MnCo 2 O 4 –GNS/PBT composites were lower than that of pure PBT and Co 3 O 4 –GNS/PBT composites. Furthermore, the incorporation of MnCo 2 O 4 –GNS hybrids gave rise to apparent decrease of pyrolysis products containing aromatic compounds, carbonyl compounds, carbon monoxide and carbon dioxide, attributed to combined impact of physical barrier for graphene and cat O 4 for organic volatiles and carbon monoxide

The Sino-American belt study: nickel and cobalt exposure, epidemiology, and clinical considerations.

Science.gov (United States)

Hamann, Dathan; Hamann, Carsten; Li, Lin-Feng; Xiang, Hailian; Hamann, Kylin; Maibach, Howard; Taylor, James S; Thyssen, Jacob P

2012-01-01

Nickel and cobalt are common causes of metal allergy. The objective of this study was to investigate nickel and cobalt exposure in belt buckles by testing 701 belts purchased in China and the United States and to consider the prevalence of nickel allergy and its relevance among Chinese patients. Seven hundred one belt buckles purchased in China and the United States were tested for nickel and cobalt release. Six hundred thirty-one Chinese patients with suspected allergic contact dermatitis were patch tested and interviewed to determine clinical relevance of results. The Chinese and American literature was reviewed to investigate trends in nickel prevalence over the past decades. Sixty percent (n = 219) of belts purchased in China (n = 365) released nickel, and 0.5% (n = 2) released cobalt; 55.7% (n = 187) in the United States (n = 336) released nickel, and 0.9% (n = 3) released cobalt. Belt dermatitis was a significant clinical finding in 34.8% of Chinese nickel-allergic patients. Literature review suggests increasing nickel allergy prevalence in the United States and China. Metallic belt buckles are an important source of nickel exposure to consumers. Belts from lowest socioeconomic vendors were more likely to release nickel. Belts with silver color and dark metallic color were more likely to release nickel and cobalt, respectively. Clinical findings show belt dermatitis in China to be a problem.

Influence of Cobalt on the Properties of Load-Sensitive Magnesium Alloys

Directory of Open Access Journals (Sweden)

Kai Kerber

2012-12-01

Full Text Available In this study, magnesium is alloyed with varying amounts of the ferromagnetic alloying element cobalt in order to obtain lightweight load-sensitive materials with sensory properties which allow an online-monitoring of mechanical forces applied to components made from Mg-Co alloys. An optimized casting process with the use of extruded Mg-Co powder rods is utilized which enables the production of magnetic magnesium alloys with a reproducible Co concentration. The efficiency of the casting process is confirmed by SEM analyses. Microstructures and Co-rich precipitations of various Mg-Co alloys are investigated by means of EDS and XRD analyses. The Mg-Co alloys’ mechanical strengths are determined by tensile tests. Magnetic properties of the Mg-Co sensor alloys depending on the cobalt content and the acting mechanical load are measured utilizing the harmonic analysis of eddy-current signals. Within the scope of this work, the influence of the element cobalt on magnesium is investigated in detail and an optimal cobalt concentration is defined based on the performed examinations.

Novel cobalt releasing sol-gel derived bioactive glass for bone tissue engineering

International Nuclear Information System (INIS)

Oliveira, Ana Celeste Ximenes; Barrioni, Breno Rocha; Leite, Maria de Fatima; Pereira, Marivalda Magalhaes

2016-01-01

Full text: Bone defects are caused by traumas, congenital disorders or infections, and bone grafts are the usual treatment. However, limitations of this therapy have lead to the advance of tissue engineering approaches. Bioactive glasses (BG) are an attractive bioactive ceramic for bone repair [1], due to its osteogenic properties and capability of releasing different ions, inducing specific biological responses. Tissue repair depends also on blood vessels formation. Among angiogenic agents, cobalt ion has been regarded as strategic component to incorporate into ion releasing materials. In this study, 5% (molar) cobalt releasing BG was synthesized by sol-gel method. To characterize the material, powder samples were evaluated by FTIR and DRX. To access the cytotoxic effects, MTT and LIVE/DEAD tests were performed on osteoblasts exposed to the ionic product of the material (100 μg/mL) for 72h. FTIR analysis reveals typical absorption bands of present groups in BG. X-ray diffractogram of DRX confirmed the amorphous character of BG, without the occurrence of recrystallization of cobalt precursor, suggesting that cobalt incorporation was well succeeded. MTT test showed that cells exposed to ionic product presented high levels of metabolic activity. LIVE/DEAD assay evidenced that cell membrane integrity and intracellular esterases activity were preserved. Both cytotoxic tests proved that cobalt-BG material generated a cell friendly environment. This work shows that BG with cobalt agent presented proper structural features and a non-cytotoxic behaviour. Reference: [1] Hench LL, J Mater Sci Mater Med 17(11), 967-78 (2006). (author)

Catalysis by transition metal compounds

International Nuclear Information System (INIS)

Klein, D.L.

1978-01-01

The catalytic properties of cobalt oxide (Co0) were investigated theoretically. The interactions of atomic hydrogen with small clusters of atoms, representing cobalt oxide surfaces, were calculated using the ab initio Unrestricted Hartree-Fock (UHF) method. The electronic structure of the bulk solid was studied through band and cluster models. The bulk electronic structure computed predicts insulating behavior for cobalt oxide and agrees with experimental optical results. The ''perfect'' (100) cobalt oxide surface was determined not to chemisorb atomic hydrogen. Singly-ionized oxygen ions located near cation vacancies were found to chemisorb hydrogen, forming two-center covalent bonds. The effect of lattice defects on the creation of singly ionized oxygen ions was examined. A systematic procedure for the study of surface and bulk electronic properties was discussed

Synthesis and characterization of cobalt-nichel oxides for the oxygen formation reaction; Sintesis y caracterizacion de oxidos de cobalto-niquel para la reaccion de formacion de oxigeno

Energy Technology Data Exchange (ETDEWEB)

Morales G, P

2001-07-01

In this work the compounds of cobalt and nickel oxides and the mixtures of cobalt-nickel were prepared which were characterized and evaluated as electrocatalysts in the oxygen release reaction in alkaline media. The compounds were synthesised by the sol-gel method: heated at 400 and 500 Centigrade. The compounds characterization was realized by thermogravimetry, X-ray diffraction and Scanning electron microscopy. As the Co{sub 3}O{sub 4} and the Ni O as the mixtures Ni O/Co{sub 3}O{sub 4} were obtained as a porous material with a small particle size, characteristics which are presented by cause of the low temperature of synthesis. The electrocatalytic evaluation for the synthesised compounds for the oxygen release reaction was realized by cyclic volt amperometry in a 0.5M KOH solution. The oxides mixtures presented a well electrocatalytic activity to be used in the electrochemical release of oxygen. The current density and the electrochemically active area, in all the cases of mixtures is very higher to the Co{sub 3}O{sub 4} and Ni O ones. Observing with greater clearness the synergic effects, in the obtained mixture at 400 C. The oxides mixtures heated at 400 C were stables for the oxygen formation reaction. Therefore it is be able to say that the Ni O/Co{sub 3}O{sub 4} mixture counts on a great reactive area: electrocatalytic characteristic desirable to be a material used as anode in the electrolysis of water, which increases the oxygen release in the anode and so the hydrogen release in the cathode. (Author)

Controlling of morphology and electrocatalytic properties of cobalt oxide nanostructures prepared by potentiodynamic deposition method

Energy Technology Data Exchange (ETDEWEB)

Hallaj, Rahman [Department of Chemistry, University of Kurdistan, P.O. Box 416, Sanandaj (Iran, Islamic Republic of); Akhtari, Keivan [Department of Chemistry, University of Kurdistan, P.O. Box 416, Sanandaj (Iran, Islamic Republic of); Research Center for Nanotechnology, University of Kurdistan, P.O.Box 416, Sanandaj (Iran, Islamic Republic of); Salimi, Abdollah, E-mail: absalimi@uok.ac.ir [Department of Chemistry, University of Kurdistan, P.O. Box 416, Sanandaj (Iran, Islamic Republic of); Research Center for Nanotechnology, University of Kurdistan, P.O.Box 416, Sanandaj (Iran, Islamic Republic of); Soltanian, Saied [Department of Physics, University of Kurdistan, P.O. Box 416, Sanandaj (Iran, Islamic Republic of)

2013-07-01

Electrodeposited cobalt oxide nanostructures were prepared by Repetitive Triangular Potential Scans (RTPS) as a simple, remarkably fast and scalable potentiodynamic method. Electrochemical deposition of cobalt oxide nanostructures onto GC electrode was performed from aqueous Co(NO{sub 3}){sub 2}, (pH 6) solution using cyclic voltammetry method. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) were used to characterize the morphology of fabricated nanostructures. The evaluation of electrochemical properties of deposited films was performed using cyclic voltametry (CV) and impedance spectroscopy (IS) techniques. The analysis of the experimental data clearly showed that the variations of potential scanning ranges during deposition process have drastic effects on the geometry, chemical structure and particle size of cobalt oxide nanoparticles. In addition, the electrochemical and electrocatalytic properties of prepared nanostructures can be controlled through applying different potential windows in electrodeposition process. The imaging and voltammetric studies suggested to the existence of at least three different shapes of cobalt-oxide nanostructures in various potential windows applied for electrodeposition. With enlarging the applied potential window, the spherical-like cobalt oxide nanoparticles with particles sizes about 30–50 nm changed to the grain-like structures (30 nm × 80 nm) and then to the worm-like cobalt oxide nanostructures with 30 nm diameter and 200–400 nm in length. Furthermore, the roughness of the prepared nanostructures increased with increasing positive potential window. The GC electrodes modified with cobalt oxide nanostructures shows excellent electrocatalytic activity toward H{sub 2}O{sub 2} and As (III) oxidation. The electrocatalytic activity of cobalt oxide nanostructures prepared at more positive potential window toward hydrogen peroxide oxidation was increased, while for As(III) oxidation the electrocatalytic

Controlling of morphology and electrocatalytic properties of cobalt oxide nanostructures prepared by potentiodynamic deposition method

International Nuclear Information System (INIS)

Hallaj, Rahman; Akhtari, Keivan; Salimi, Abdollah; Soltanian, Saied

2013-01-01

Electrodeposited cobalt oxide nanostructures were prepared by Repetitive Triangular Potential Scans (RTPS) as a simple, remarkably fast and scalable potentiodynamic method. Electrochemical deposition of cobalt oxide nanostructures onto GC electrode was performed from aqueous Co(NO 3 ) 2 , (pH 6) solution using cyclic voltammetry method. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) were used to characterize the morphology of fabricated nanostructures. The evaluation of electrochemical properties of deposited films was performed using cyclic voltametry (CV) and impedance spectroscopy (IS) techniques. The analysis of the experimental data clearly showed that the variations of potential scanning ranges during deposition process have drastic effects on the geometry, chemical structure and particle size of cobalt oxide nanoparticles. In addition, the electrochemical and electrocatalytic properties of prepared nanostructures can be controlled through applying different potential windows in electrodeposition process. The imaging and voltammetric studies suggested to the existence of at least three different shapes of cobalt-oxide nanostructures in various potential windows applied for electrodeposition. With enlarging the applied potential window, the spherical-like cobalt oxide nanoparticles with particles sizes about 30–50 nm changed to the grain-like structures (30 nm × 80 nm) and then to the worm-like cobalt oxide nanostructures with 30 nm diameter and 200–400 nm in length. Furthermore, the roughness of the prepared nanostructures increased with increasing positive potential window. The GC electrodes modified with cobalt oxide nanostructures shows excellent electrocatalytic activity toward H 2 O 2 and As (III) oxidation. The electrocatalytic activity of cobalt oxide nanostructures prepared at more positive potential window toward hydrogen peroxide oxidation was increased, while for As(III) oxidation the electrocatalytic activity decreased

Responses of two scleractinian corals to cobalt pollution and ocean acidification.

Directory of Open Access Journals (Sweden)

Tom Biscéré

Full Text Available The effects of ocean acidification alone or in combination with warming on coral metabolism have been extensively investigated, whereas none of these studies consider that most coral reefs near shore are already impacted by other natural anthropogenic inputs such as metal pollution. It is likely that projected ocean acidification levels will aggravate coral reef health. We first investigated how ocean acidification interacts with one near shore locally abundant metal on the physiology of two major reef-building corals: Stylophora pistillata and Acropora muricata. Two pH levels (pHT 8.02; pCO2 366 μatm and pHT 7.75; pCO2 1140 μatm and two cobalt concentrations (natural, 0.03 μg L-1 and polluted, 0.2 μg L-1 were tested during five weeks in aquaria. We found that, for both species, cobalt input decreased significantly their growth rates by 28% while it stimulated their photosystem II, with higher values of rETRmax (relative Electron Transport Rate. Elevated pCO2 levels acted differently on the coral rETRmax values and did not affect their growth rates. No consistent interaction was found between pCO2 levels and cobalt concentrations. We also measured in situ the effect of higher cobalt concentrations (1.06 ± 0.16 μg L-1 on A. muricata using benthic chamber experiments. At this elevated concentration, cobalt decreased simultaneously coral growth and photosynthetic rates, indicating that the toxic threshold for this pollutant has been reached for both host cells and zooxanthellae. Our results from both aquaria and in situ experiments, suggest that these coral species are not particularly sensitive to high pCO2 conditions but they are to ecologically relevant cobalt concentrations. Our study reveals that some reefs may be yet subjected to deleterious pollution levels, and even if no interaction between pCO2 levels and cobalt concentration has been found, it is likely that coral metabolism will be weakened if they are subjected to additional

Nano cobalt oxides for photocatalytic hydrogen production

KAUST Repository

Mangrulkar, Priti A.; Joshi, Meenal M.; Tijare, Saumitra N.; Polshettiwar, Vivek; Labhsetwar, Nitin K.; Rayalu, Sadhana Suresh

2012-01-01

of various operating parameters in hydrogen generation by nano cobalt oxide was then studied in detail. Copyright © 2012, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.

Cobalt 60 commercial irradiation facilities

International Nuclear Information System (INIS)

West, G.

1985-01-01

The advantage of using cobalt 60 for ionizing treatment is that it has excellent penetration. Gamma plants are also very efficient, in as much as there is very little mechanical or electrical equipment in a gamma irradiation facility. The average efficiency of a gamma plant is usually around 95% of all available processing time

Synthesis, characterization and thermal analysis of polyimide-cobalt ferrite nanocomposites

International Nuclear Information System (INIS)

Mazuera, David; Perales, Oscar; Suarez, Marcelo; Singh, Surinder

2010-01-01

Research highlights: · Polyimide-cobalt ferrite nanocomposites were successfully produced. · Produced nanocomposites are suitable for use at temperatures below 80 deg. C. · Magnetic properties of nanocomposites were no sensitive to particle agglomeration. · Good distribution of clustered nanoparticles was achieved in produced composites. - Abstract: Cobalt ferrite nanocrystals were synthesized under size-controlled conditions in aqueous phase and incorporated into a polyimide matrix at various volumetric loads. Synthesized 20 nm cobalt ferrite single crystals, which exhibited a room-temperature coercivity of 2.9 kOe, were dispersed in polyimide precursor using two techniques: homogenizer and ball milling. These suspensions were then cured to develop the polyimide structure in the resulting nanocomposites. Produced films were characterized by Fourier transform infrared spectroscopy, X-ray diffraction and vibrating sample magnetometry, which confirmed the formation of the desired phases. As expected, the saturation magnetization in the nanocomposites varied according to the polyimide/ferrite weight ratio, while coercivity remained at the value corresponding to pure cobalt ferrite nanocrystals. Thermal degradation, thermal stability and dynamic mechanical analyses tests were also carried out to assess the effect of the concentration of the ferrite disperse phase on the thermo-mechanical behavior of the corresponding nanocomposites as well as the used dispersion techniques.

Isolation and characterization of cobalt-sensitive mutant of Neurospora crassa

Directory of Open Access Journals (Sweden)

Krishnapuram Rashmi

2014-12-01

Full Text Available Objective: To isolate and demonstrate the mechanism of metal transport in cobalt-sensitive mutant (CSM of Neurospora crassa (N. crassa. Methods: Isolation of CSM of N. crassa, I50 determination, growth measurements, metal ion uptake studies and sexual crosses were performed to determine the mechanism of sensitivity and locus. Results: CSMs of N. crassa were isolated by mutagenesis with diethyl sulfate. More than 500 isolates were screened and out of these isolates, CSM-I was 5-fold and CSM-II was 10-fold sensitive to Co on liquid medium as compared to the wild type. Compositional analysis of cell wall revealed the decrease in total phosphate content. N. crassa CSM bound much less cobalt to cell wall fraction than wild type. The data indicated closer linkage between resistance and mating type locus (mat, which is, located on LG I. Conclusions: A CSM of N. crassa is 5-fold more sensitive than wild type and cross sensitive to nickel and copper and hyper-accumulates 2-4 fold more toxic metal ions over wild type. The mechanism for sensitivity is decreased in cobalt-binding to cell wall fraction and increased intracellular uptake. N. crassa-acon-3 morphologically resembles the CSM, cobalt-sensitive and maps to similar locus.

Fe(II)-substituted cobalt ferrite nanoparticles against multidrug resistant microorganisms

Science.gov (United States)

Žalnėravičius, Rokas; Paškevičius, Algimantas; Mažeika, Kęstutis; Jagminas, Arūnas

2018-03-01

The present study is focused on the determination the influence of cobalt content in the magnetic cobalt ferrite nanoparticles (Nps) on their antibacterial efficiency against gram-negative Escherichia coli and gram-positive Staphylococcus aureus bacteria and several Candida species, in particular C. parapsilosis and C. albicans. For the synthesis of Fe(II) substituted cobalt ferrite Nps by co-precipitation way, the L-lysine was used as the capping biocompatible agent and the particle size was successfully controlled to be in the range of 5-6.4 nm. The antimicrobial efficiencies of the CoxFe1-xFe2O4@Lys Nps, where x varies from 0.2 to 1.0, were evaluated through the quantitative analysis by comparing with that of Fe3O4@Lys Nps and L-lysine. In this way, it was evidenced that increase in the Co2+ content in the similar sized cobalt ferrite Nps resulted in an increase in their antimicrobial potency into 93.1-86.3 % for eukaryotic and into 96.4-42.7 % for prokaryotic strains. For characterization the composition, structure, and morphology of the tested herein Nps inductively coupled plasma optical emission spectrometry, X-ray diffraction, high-resolution transmission electron microscopy, Mössbauer, and FTIR spectroscopy techniques were conferred.

The cobalt spot test - further insights into its performance and use

DEFF Research Database (Denmark)

Midander, Klara; Julander, Anneli; Skare, Lizbet

2013-01-01

A spot test was recently developed for easy and rapid testing to detect whether cobalt is available on surfaces in contact with skin.......A spot test was recently developed for easy and rapid testing to detect whether cobalt is available on surfaces in contact with skin....

Computer simulation of the vertical growth of subsurface cobalt nanoclusters in gold

NARCIS (Netherlands)

Kulikov, D.V.; Kurnosikov, O.; Sicot, M.V.; Trushin, Yu.V.

2009-01-01

The vertical growth of nanodimensional cobalt clusters buried under the surface of a gold substrate has been studied using computer simulation methods with allowance for the interdiffusion of Au and Co atoms and the fields of elastic stresses generated by cobalt clusters in the gold matrix. The

Cobalt supported on carbon nanofibers as catalysts for the Fischer-Tropsch synthesis

NARCIS (Netherlands)

Bezemer, G.L.

2006-01-01

The Fischer-Tropsch (FT) process converts synthesis gas (H2/CO) over a heterogeneous catalyst into hydrocarbons. Generally, cobalt catalysts supported on oxidic carriers are used for the FT process, however it appears to be difficult to obtain and maintain fully reduced cobalt particles. To overcome

Absolute measurement of the critical scattering cross section in cobalt

International Nuclear Information System (INIS)

Glinka, C.J.; Minkiewicz, V.J.; Passell, L.

1975-01-01

Small-angle neutron scattering techniques have been used to study the angular distribution of the critical scattering from cobalt above T/sub c/. These measurements have been put on an absolute scale by calibrating the critical scattering directly against the nuclear incoherent scattering from cobalt. In this way the interaction range r 1 , which appears in the classical and modified Ornstein--Zernike expressions for the asymptotic form of the spin pair correlation function and is related to the strength of the spin correlations, has been determined. We obtain r 1 /a = 0.46 +- 0.03 for the ratio of the interaction range to the nearest-neighbor distance in cobalt. This result is in good agreement with theoretical predictions. Lack of agreement among previous determinations of the ratio r 1 /a made in iron failed to provide a definitive comparison with theory

Temperature and fluence effects in lead implanted cobalt single crystals

International Nuclear Information System (INIS)

Johansen, A.; Sarholt-Kristensen, L.; Johnson, E.; Steenstrup, S.; Chernysh, V.S.

1988-01-01

The channeled sputtering yields of the hcp and fcc phases of cobalt depend on the crystal structure and the radiation induced damage. Earlier irradiations of cobalt with argon ions channeled in the hcp direction give sputtering yields higher than expected in the temperature range 100-350deg C. This effect was attributed to a combination of radiation induced damage and a possible implantation induced hcp --> fcc phase transition. Sputtering yields for cobalt single crystals irradiated with 150 keV Pb + ions along the direction of the hcp phase and the direction of the fcc phase have been measured using the weightloss method. The radiation damage and the amount of lead retained in the implanted surface has been investigated by 'in situ' RBS/channeling analysis. Measured partial sputtering yields of lead ≅ 1 atom/ion indicate preferential sputtering of lead atoms. (orig.)

Reactions of 3d-series metallocenes with organic cadmium compounds

International Nuclear Information System (INIS)

Razuvaev, G.A.; Mar'in, V.P.; Vyshinskaya, L.I.; Grinval'd, I.I.; Spiridonova, N.N.

1987-01-01

Interaction of organic cadmium compounds and 3d-series metallocenes, Cp 2 M (M=V, Cr, Mn, Ni, Co) has been studied. It is shown that direction of these reactions is determined by metallocene nature. Reactions of oxidizing addition leading to σ-complexes formation are characteristic for vanadium and chromium metallocenes. When reacting cobaltocene with R 2 Cd, R group introduction to cyclopentadienyl ring and elimination of cobalt diene complexes take place. Manganocene and nickelocene interaction goes through the stage of complex formation with transition metal - cadmium bond

Improvement of the oxidation stability of cobalt nanoparticles

Directory of Open Access Journals (Sweden)

Celin Dobbrow

2012-01-01

Full Text Available In order to enhance the resistance of cobalt nanoparticles to oxidation in air, the impact of different stabilization strategies on the isothermal oxidation of particle dispersions and powders was kinetically investigated and compared to as-prepared particle preparations. A post-synthesis treatment with different alcohols was employed, and we also investigate the influence of two different polymer shells on the oxidation process. We found a parabolic decrease of the magnetization for all particle charges, indicating that the process is dominated by a diffusion of oxygen to the cobalt core and a radial growth of the oxide layer from the particle surface to the core. A significant deceleration of the oxidation process was observed for all alcohol-passivated particle preparations, and this resulted finally in a stagnation effect. The stabilizing effect increases in the sequence Co@OA/MeOH < Co@OA/EtOH < Co@OA/iPrOH. For polymer-coated particle preparations Co@PCL and Co@PS, the deceleration was even more pronounced. The results demonstrate that cobalt nanoparticles can effectively be protected against oxidation in order to improve their mid- to longterm stability.

A computer controlled tele-cobalt unit

International Nuclear Information System (INIS)

Brace, J.A.

1982-01-01

A computer controlled cobalt treatment unit was commissioned for treating patients in January 1980. Initially the controlling computer was a minicomputer, but now the control of the therapy unit is by a microcomputer. The treatment files, which specify the movement and configurations necessary to deliver the prescribed dose, are produced on the minicomputer and then transferred to the microcomputer using minitape cartridges. The actual treatment unit is based on a standard cobalt unit with a few additional features e.g. the drive motors can be controlled either by the computer or manually. Since the treatment unit is used for both manual and automatic treatments, the operational procedure under computer control is made to closely follow the manual procedure for a single field treatment. The necessary safety features which protect against human, hardware and software errors as well as the advantages and disadvantages of computer controlled radiotherapy are discussed

Electro-activity of cobalt and nickel complexes for the reduction of protons into di-hydrogen. Application to PEM water electrolysis

International Nuclear Information System (INIS)

Pantani, O.; Anxolabehere, E.; Aukauloo, A.; Millet, P.

2006-01-01

Proton exchange membrane (PEM) water electrolysis is a safe and efficient way to perform water splitting into di-hydrogen and di-oxygen. In a PEM water electrolyser, platinum is commonly used as electro-catalyst on the cathodic side of the cells, mostly because of its efficiency for hydrogen evolution. But for cost considerations, there is a need to find alternative low-cost electrocatalysts. Molecular chemistry offers the possibility of synthesizing new compounds for this purpose, such as transition metal complexes. Results obtained with nickel- and cobalt-oximes compounds are presented in this paper. They have been chemically (1H NMR, EPR) and electrochemically (voltametry, spectro-electrochemistry) characterized. Their ability to electrochemically reduce protons into di-hydrogen when they are either dissolved in solution or immobilized at the surface of a solid electrode is discussed. (authors)

Facile fabrication of cobalt oxalate nanostructures with superior specific capacitance and super-long cycling stability

Science.gov (United States)

Cheng, Guanhua; Si, Conghui; Zhang, Jie; Wang, Ying; Yang, Wanfeng; Dong, Chaoqun; Zhang, Zhonghua

2016-04-01

Transition metal oxalate materials have shown huge competitive advantages for applications in supercapacitors. Herein, nanostructured cobalt oxalate supported on cobalt foils has been facilely fabricated by anodization, and could directly serve as additive/binder-free electrodes for supercapacitors. The as-prepared cobalt oxalate electrodes present superior specific capacitance of 1269 F g-1 at the current density of 6 A g-1 in the galvanostatic charge/discharge test. Moreover, the retained capacitance is as high as 87.2% as the current density increases from 6 A g-1 to 30 A g-1. More importantly, the specific capacitance of cobalt oxalate retains 91.9% even after super-long cycling of 100,000 cycles. In addition, an asymmetric supercapacitor assembled with cobalt oxalate (positive electrode) and activated carbon (negative electrode) demonstrates excellent capacitive performance with high energy density and power density.

Dissolution of manganese and cobalt and their deposition on Type 304 stainless steel in liquid sodium

International Nuclear Information System (INIS)

Yokota, Norikatsu; Shimoyashiki, Shigehiro

1989-01-01

Dissolution of manganese and cobalt and their deposition on Type 304 stainless steel in liquid sodium at 833 K for 3.6 x 10 3 ks were examined using a liquid sodium pot. Manganese was easily dissolved in sodium from the iron-manganese alloy specimen and deposited on the steel to form two kind of deposition particles, α-phase (body-centered cubic) composed of iron and γ-phase (face-centered cubic) composed of iron and manganese, respectively. Cobalt which was less easily dissolved than manganese also deposited on the Type 304 stainless steel, giving an iron-cobalt alloy. These three deposition particles corresponded to the precipitation lines of iron-manganese and iron-cobalt phase diagrams at 833 K, respectively. Therefore, the deposition process of manganese or cobalt in sodium was explained as a precipitation process of iron-manganese or iron-cobalt in the solid region of the binary phase diagram. A sodium chromite (NaCrO 2 ) layer was formed on the steel surface. (author)

Cobalt Ferrite Nanocrystallites for Sustainable Hydrogen Production Application

Directory of Open Access Journals (Sweden)

Rajendra S. Gaikwad

2011-01-01

Full Text Available Cobalt ferrite, CoFe2O4, nanocrystalline films were deposited using electrostatic spray method and explored in sustainable hydrogen production application. Reflection planes in X-ray diffraction pattern confirm CoFe2O4 phase. The surface scanning microscopy photoimages reveal an agglomeration of closely-packed CoFe2O4 nanoflakes. Concentrated solar-panel, a two-step water splitting process, measurement technique was preferred for measuring the hydrogen generation rate. For about 5 hr sustainable, 440 mL/hr, hydrogen production activity was achieved, confirming the efficient use of cobalt ferrite nanocrystallites film in hydrogen production application.

Racemic cobalt phosphonates incorporating flexible bis(imidazole) co-ligands.

Science.gov (United States)

Feng, Jian-Shen; Cai, Zhong-Sheng; Ren, Min; Bao, Song-Song; Zheng, Li-Min

2015-11-07

By incorporating flexible bis(imidazol-1-ylmethyl)benzene (bix) co-ligands, four new racemic cobalt phosphonates with formulae Co3(3-ppap)2(1,4-bix)2(H2O)4·4H2O (1), Co3(3-ppap)2(1,3-bix)2(H2O)4·5H2O (2), Co3(3-ppap)2(1,2-bix)2(H2O)4·4H2O (3) and Co3(ppa)2(1,2-bix)2·4H2O (4) are isolated, where 3-ppapH3 represents 3-phenyl-3-((phosphonomethyl)amino)propanoic acid and ppaH3 is 2-phenyl-2-(phosphonomethylamino)acetic acid. Compounds 1-3 crystallize in the monoclinic space group P21/c and show two-dimensional structures in which the Co3(3-ppap)2 chains are bridged by 1,4-bix, 1,3-bix and 1,2-bix ligands in trans-modes, respectively. Within the chain, a racemic dimer of Co2(3-ppap)2(2-) is found, where the Co atoms are doubly bridged by O-P-O units from the (S)- and (R)-3-ppap(3-) ligands. The dimers are connected by another crystallographically independent Co atom through O-P-O linkages to form an infinite racemic chain. The packing modes of the layers in 1-3 are quite different, however, which are ABAB in the cases of 1 and 3 while ABCDABCD in the case of 2, attributed to the positional isomerism of the bix co-ligands. Compound 4 displays a chain structure in which the 1,2-bix bridges the Co atoms in cis-mode within the chain. Magnetic properties are investigated for all compounds.

Model for cobalt 60/58 deposition on primary coolant piping in a boiling water reactor

International Nuclear Information System (INIS)

Dehollander, W.R.

1979-01-01

A first principles model for deposition of radioactive metals into the corrosion films of primary coolant piping is proposed. It is shown that the predominant mechanism is the inclusion of the radioactive species such as Cobalt 60 into the spinel structure of the corrosion film during the act of active corrosion. This deposition can occupy only a defined fraction of the available plus 2 valence sites of the spinel. For cobalt ions, this ratio is roughly 4.6 x 10 -3 of the total iron sites. Since no distinction is made between Cobalt 60, Cobalt 58, and Cobalt 59 in this process, the radioactivity associated with this inclusion is a function of the ratio of the radioactive species to the nonradioactive species in the water causing the corrosion of the pipe metal. The other controlling parameter is the corrosion rate of the pipe material. This can be a function of time, for example, and it shown that freshly descaled metal when exposed to the cobalt containing water can incorporate as much as 10 x 10 -3 cobalt ions per iron atom in the initial corrosion period. This has implications for the problem of decontaminating nuclear reactor piping. Equations and selected observations are presented without reference to any specifically identified reactor or utility, so as to protect any proprietary interest

Influence of Reduction Promoters on Stability of Cobalt/g-Alumina Fischer-Tropsch Synthesis Catalysts

OpenAIRE

Gary Jacobs; Wenping Ma; Burtron H. Davis

2014-01-01

This focused review article underscores how metal reduction promoters can impact deactivation phenomena associated with cobalt Fischer-Tropsch synthesis catalysts. Promoters can exacerbate sintering if the additional cobalt metal clusters, formed as a result of the promoting effect, are in close proximity at the nanoscale to other cobalt particles on the surface. Recent efforts have shown that when promoters are used to facilitate the reduction of small crystallites with the aim of increasing...

Electrocatalytic miRNA Detection Using Cobalt Porphyrin-Modified Reduced Graphene Oxide

Directory of Open Access Journals (Sweden)

Camille De Souza

2014-06-01

Full Text Available Metalated porphyrins have been described to bind nucleic acids. Additionally, cobalt porphyrins present catalytic properties towards oxygen reduction. In this work, a carboxylic acid-functionalized cobalt porphyrin was physisorbed on reduced graphene oxide, then immobilized on glassy carbon electrodes. The carboxylic groups were used to covalently graft amino-terminated oligonucleotide probes which are complementary to a short microRNA target. It was shown that the catalytic oxygen electroreduction on cobalt porphyrin increases upon hybridization of miRNA strand (“signal-on” response. Current changes are amplified compared to non-catalytic amperometric system. Apart from oxygen, no added reagent is necessary. A limit of detection in the sub-nanomolar range was reached. This approach has never been described in the literature.

Cobalt chloride administration in athletes: a new perspective in blood doping?

Science.gov (United States)

Lippi, G; Franchini, M; Guidi, G C

2005-11-01

Blood doping is an illegal and unfair way of enhancing athletic performance by increasing the oxygen carrying capacity of the blood. Currently used methods usually involve stimulation of erythropoiesis. Gene therapy targeting the hypoxia inducible factor pathway may be an attractive alternative to traditional blood doping techniques. Hypoxia activates a large number of genes with essential roles in cell and tissue adaptation to low oxygen. Cobalt chloride is a well established chemical inducer of hypoxia-like responses such as erythropoiesis. Cobalt supplementation is not banned and therefore would not be detected by current anti-doping testing. Although there is as yet no direct or anecdotal evidence of cobalt chloride administration to athletes, its use should be warned against as being not only unfair but potentially dangerous.

Synthesis of superconducting cobalt oxyhydrates using a novel method: Electrolyzed and oxidized water

International Nuclear Information System (INIS)

Liu, C.-J.; Wu, T.-H.; Hsu, L.-L.; Wang, J.-S.; Chen, S.-Y.

2007-01-01

By deintercalation of Na + followed by inserting bilayers of water molecules into the host lattice, the layered cobalt oxide of γ-Na 0.7 CoO 2 undergoes a topotactic transformation to a layered cobalt oxyhydrate of Na 0.35 (H 2 O) 1.3 CoO 2-δ with the c-axis expanded from c ∼ 10.9 A to c ∼ 19.6 A. In this paper, we demonstrate that the superconducting phase of c ∼ 19.6 A can be directly obtained by simply immersing γ-Na 0.7 CoO 2 powders in electrolyzed/oxidized (EO) water, which is readily available from a commercial electrolyzed water generator. We found that high oxidation-reduction potential of EO water drives the oxidation of the cobalt ions accompanying by the formation of the superconductive c ∼ 19.6 A phase. Our results demonstrate how EO water can be used to oxidize the cobalt ions and hence form superconducting cobalt oxyhydrates in a clean and simple way and may provide an economic and environment-friendly route to oxidize the transition metal of complex metal oxides

Synthesis of superconducting cobalt oxyhydrates using a novel method: Electrolyzed and oxidized water

Science.gov (United States)

Liu, Chia-Jyi; Wu, Tsung-Hsien; Hsu, Lin-Li; Wang, Jung-Sheng; Chen, Shu-Yo

2007-09-01

By deintercalation of Na+ followed by inserting bilayers of water molecules into the host lattice, the layered cobalt oxide of γ-Na0.7CoO2 undergoes a topotactic transformation to a layered cobalt oxyhydrate of Na0.35(H2O)1.3CoO2-δ with the c-axis expanded from c ≈ 10.9 Å to c ≈ 19.6 Å. In this paper, we demonstrate that the superconducting phase of c ≈ 19.6 Å can be directly obtained by simply immersing γ-Na0.7CoO2 powders in electrolyzed/oxidized (EO) water, which is readily available from a commercial electrolyzed water generator. We found that high oxidation-reduction potential of EO water drives the oxidation of the cobalt ions accompanying by the formation of the superconductive c ≈ 19.6 Å phase. Our results demonstrate how EO water can be used to oxidize the cobalt ions and hence form superconducting cobalt oxyhydrates in a clean and simple way and may provide an economic and environment-friendly route to oxidize the transition metal of complex metal oxides.

Synthesis of superconducting cobalt oxyhydrates using a novel method: Electrolyzed and oxidized water

Energy Technology Data Exchange (ETDEWEB)

Liu, C.-J. [Department of Physics, National Changhua University of Education, Changhua 50007, Taiwan (China)], E-mail: liucj@cc.ncue.edu.tw; Wu, T.-H.; Hsu, L.-L.; Wang, J.-S.; Chen, S.-Y. [Department of Physics, National Changhua University of Education, Changhua 50007, Taiwan (China)

2007-09-01

By deintercalation of Na{sup +} followed by inserting bilayers of water molecules into the host lattice, the layered cobalt oxide of {gamma}-Na{sub 0.7}CoO{sub 2} undergoes a topotactic transformation to a layered cobalt oxyhydrate of Na{sub 0.35}(H{sub 2}O){sub 1.3}CoO{sub 2-{delta}} with the c-axis expanded from c {approx} 10.9 A to c {approx} 19.6 A. In this paper, we demonstrate that the superconducting phase of c {approx} 19.6 A can be directly obtained by simply immersing {gamma}-Na{sub 0.7}CoO{sub 2} powders in electrolyzed/oxidized (EO) water, which is readily available from a commercial electrolyzed water generator. We found that high oxidation-reduction potential of EO water drives the oxidation of the cobalt ions accompanying by the formation of the superconductive c {approx} 19.6 A phase. Our results demonstrate how EO water can be used to oxidize the cobalt ions and hence form superconducting cobalt oxyhydrates in a clean and simple way and may provide an economic and environment-friendly route to oxidize the transition metal of complex metal oxides.

Concerning the Deactivation of Cobalt(III)-Based Porphyrin and Salen Catalysts in Epoxide/CO 2 Copolymerization

KAUST Repository

Xia, Wei

2015-02-05

© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. Functioning as active catalysts for propylene oxide (PO) and carbon dioxide copolymerization, cobalt(III)-based salen and porphyrin complexes have drawn great attention owing to their readily modifiable nature and promising catalytic behavior, such as high selectivity for the copolymer formation and good regioselectivity with respect to the polymer microstructure. Both cobalt(III)-salen and porphyrin catalysts have been found to undergo reduction reactions to their corresponding catalytically inactive cobalt(II) species in the presence of propylene oxide, as evidenced by UV/Vis and NMR spectroscopies and X-ray crystallography (for cobalt(II)-salen). Further investigations on a TPPCoCl (TPP=tetraphenylporphyrin) and NaOMe system reveal that such a catalyst reduction is attributed to the presence of alkoxide anions. Kinetic studies of the redox reaction of TPPCoCl with NaOMe suggests a pseudo-first order in cobalt(III)-porphyrin. The addition of a co-catalyst, namely bis(triphenylphosphine)iminium chloride (PPNCl), into the reaction system of cobalt(III)-salen/porphyrin and PO shows no direct stabilizing effect. However, the results of PO/CO2 copolymerization by cobalt(III)-salen/porphyrin with PPNCl suggest a suppressed catalyst reduction. This phenomenon is explained by a rapid transformation of the alkoxide into the carbonate chain end in the course of the polymer formation, greatly shortening the lifetime of the autoreducible PO-ring-opening intermediates, cobalt(III)-salen/porphyrin alkoxides. CO2 saves: The deactivation of cobalt(III)-porphyrin and salen catalysts in propylene oxide/carbon dioxide copolymerization is systematically investigated, revealing a proposed mechanism for the catalyst reduction (see scheme).

Structural and magnetic properties of the products of the transformation of ferrihydrite: Effect of cobalt dications

Energy Technology Data Exchange (ETDEWEB)

Camacho, K.I. [Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional Unidad Saltillo, Av. Industria Metalúrgica 1062, Parque Industrial Ramos Arizpe, Ramos Arizpe, Coahuila C.P.25000, México (Mexico); Pariona, N. [Red de Estudios Moleculares Avanzados, Instituto de Ecología A.C., Carretera Antigua a Coatepec 351, El Haya, 91070 Xalapa, Veracruz (Mexico); Martinez, A.I., E-mail: arturo.martinez@cinvestav.edu.mx [Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional Unidad Saltillo, Av. Industria Metalúrgica 1062, Parque Industrial Ramos Arizpe, Ramos Arizpe, Coahuila C.P.25000, México (Mexico); Baggio-Saitovitch, E. [Centro Brasileiro de Pesquisas Físicas, Río de Janeiro 22290-180 (Brazil); Herrera-Trejo, M. [Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional Unidad Saltillo, Av. Industria Metalúrgica 1062, Parque Industrial Ramos Arizpe, Ramos Arizpe, Coahuila C.P.25000, México (Mexico); Perry, Dale L. [Mailstop 70A1150, Lawrence Berkeley National Laboratory, University of California, Berkeley, CA 94720 (United States)

2017-05-01

The effect of cobalt dications on the transformation of 2-line ferrihydrite (2LF) has been studied. The products of the transformation reaction were characterized by X-ray diffraction, Mössbauer spectroscopy (MS), transmission electron microscopy (TEM), magnetometry, and first-order reversal curve (FORC) diagrams. It was found that the concentration of cobalt dications plays an important role on the structural and magnetic properties of the products; i.e., for low cobalt concentrations, cobalt-substituted hematite is formed, while higher concentrations promote the formation of cobalt-substituted magnetite. Structural results revealed that formation of other iron oxide polymorphs is avoided and residual 2LF is always present in the final products. In this way, hematite/2LF and magnetite/2LF nanocomposites were formed. For all the samples, magnetic measurements yielded non-saturated hysteresis loops at a maximum field of 12 kOe. For cobalt-substituted hematite/2LF samples, FORC diagrams revealed the presence of multiple single-domain (SD) components which generate interaction coupling between SD with low and high coercivity. Moreover, for cobalt-substituted magnetite/2LF samples, the FORC diagrams revealed the components of wasp-waist hysteresis loops which consist of mixtures of SD and superparamagnetic particles. One of the goals of the present study is the rigorous, experimental documentation of ferrihydrite/hematite mixtures as a function of reaction conditions for use as analytical standards research. - Highlights: • Co(II) may stabilize ferrihydrite against transformation to more crystalline oxides. • The transformation is strongly dependent on the Co(II)/Fe(III) atomic ratio. • Cobalt-substituted hematite and cobalt-substituted magnetite were the products. • FORC diagrams identified the interaction coupling between single-domains.

Structural and magnetic properties of the products of the transformation of ferrihydrite: Effect of cobalt dications

International Nuclear Information System (INIS)

Camacho, K.I.; Pariona, N.; Martinez, A.I.; Baggio-Saitovitch, E.; Herrera-Trejo, M.; Perry, Dale L.

2017-01-01

The effect of cobalt dications on the transformation of 2-line ferrihydrite (2LF) has been studied. The products of the transformation reaction were characterized by X-ray diffraction, Mössbauer spectroscopy (MS), transmission electron microscopy (TEM), magnetometry, and first-order reversal curve (FORC) diagrams. It was found that the concentration of cobalt dications plays an important role on the structural and magnetic properties of the products; i.e., for low cobalt concentrations, cobalt-substituted hematite is formed, while higher concentrations promote the formation of cobalt-substituted magnetite. Structural results revealed that formation of other iron oxide polymorphs is avoided and residual 2LF is always present in the final products. In this way, hematite/2LF and magnetite/2LF nanocomposites were formed. For all the samples, magnetic measurements yielded non-saturated hysteresis loops at a maximum field of 12 kOe. For cobalt-substituted hematite/2LF samples, FORC diagrams revealed the presence of multiple single-domain (SD) components which generate interaction coupling between SD with low and high coercivity. Moreover, for cobalt-substituted magnetite/2LF samples, the FORC diagrams revealed the components of wasp-waist hysteresis loops which consist of mixtures of SD and superparamagnetic particles. One of the goals of the present study is the rigorous, experimental documentation of ferrihydrite/hematite mixtures as a function of reaction conditions for use as analytical standards research. - Highlights: • Co(II) may stabilize ferrihydrite against transformation to more crystalline oxides. • The transformation is strongly dependent on the Co(II)/Fe(III) atomic ratio. • Cobalt-substituted hematite and cobalt-substituted magnetite were the products. • FORC diagrams identified the interaction coupling between single-domains.

Concerning the Deactivation of Cobalt(III)-Based Porphyrin and Salen Catalysts in Epoxide/CO 2 Copolymerization

KAUST Repository

Xia, Wei; Salmeia, Khalifah A.; Vagin, Sergei I.; Rieger, Bernhard

2015-01-01

© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. Functioning as active catalysts for propylene oxide (PO) and carbon dioxide copolymerization, cobalt(III)-based salen and porphyrin complexes have drawn great attention owing to their readily modifiable nature and promising catalytic behavior, such as high selectivity for the copolymer formation and good regioselectivity with respect to the polymer microstructure. Both cobalt(III)-salen and porphyrin catalysts have been found to undergo reduction reactions to their corresponding catalytically inactive cobalt(II) species in the presence of propylene oxide, as evidenced by UV/Vis and NMR spectroscopies and X-ray crystallography (for cobalt(II)-salen). Further investigations on a TPPCoCl (TPP=tetraphenylporphyrin) and NaOMe system reveal that such a catalyst reduction is attributed to the presence of alkoxide anions. Kinetic studies of the redox reaction of TPPCoCl with NaOMe suggests a pseudo-first order in cobalt(III)-porphyrin. The addition of a co-catalyst, namely bis(triphenylphosphine)iminium chloride (PPNCl), into the reaction system of cobalt(III)-salen/porphyrin and PO shows no direct stabilizing effect. However, the results of PO/CO2 copolymerization by cobalt(III)-salen/porphyrin with PPNCl suggest a suppressed catalyst reduction. This phenomenon is explained by a rapid transformation of the alkoxide into the carbonate chain end in the course of the polymer formation, greatly shortening the lifetime of the autoreducible PO-ring-opening intermediates, cobalt(III)-salen/porphyrin alkoxides. CO2 saves: The deactivation of cobalt(III)-porphyrin and salen catalysts in propylene oxide/carbon dioxide copolymerization is systematically investigated, revealing a proposed mechanism for the catalyst reduction (see scheme).

Research on rejection performance of reverse osmosis to cobalt in simulated radioactive wastewater

International Nuclear Information System (INIS)

Kong Jinsong; Tian Yanjie

2012-01-01

In order to reveal the rejection performance of the reverse osmosis applied in the radioactive wastewater treatment, treatment experiments were carried out on a pilot reverse osmosis equipment using wastewater containing cobalt nuclide. Results showed that the rejection ratio of reverse osmosis to cobalt was almost not affected by the operation pressure and the ratio of reclaiming, and had no direct relation with the salt rejection ratio. The ratio of cobalt rejection reached 90% in the experiment condition and could meet the requirement on the disposal of radioactive wastewater produced by nuclear powered installations. (authors)

Magnetic Cobalt and Cobalt Oxide Nanoparticles in Hyperbranched Polyester Polyol Matrix

Directory of Open Access Journals (Sweden)

O. I. Medvedeva

2017-01-01

Full Text Available A series of cobalt (Co and its oxides based nanoparticles were synthesized by using hyperbranched polyester polyol Boltorn H20 as a platform and sodium borohydride as a reducing agent. UV, FT-IR, XRD, NTA, and TEM methods were employed to obtain physicochemical characteristics of the products. The average diameter of Co nanoparticles was approximately 8.2±3.4 nm. Their magnetic properties, including hysteresis loop, field-cooled, and zero field-cooled curves were investigated. The nanoparticles exhibit superparamagnetism at room temperature, accompanied by magnetic hysteresis below the blocking temperature.

Solvent extractions applications to hydrometallurgy. Pt.III: Nickel, cobalt, manganese and ocean nodules

International Nuclear Information System (INIS)

Amer, S.

1981-01-01

The main applications of solvent extraction to the hydrometallurgy of nickel, cobalt, manganese and manganese rich ocean nodules, which also contain nickel, cooper and cobalt, are exposed. A short description of the processes with commercial applications is made. (author)

Effect of vitamin B12 pulse addition on the performance of cobalt deprived anaerobic granular sludge bioreactors

KAUST Repository

Fermoso, Fernando G.

2010-07-01

The effect of a pulse addition of vitamin B12 as cobalt source to restore the performance of cobalt depleted methanol-fed bioreactors was investigated. One upflow anaerobic sludge bed (UASB) reactor was supplied with a pulse of vitamin B12, and its operation was compared to that of another cobalt depleted UASB reactor to which a pulse of CoCl2 was given. The addition of cobalt in the form of CoCl2 supplies enough cobalt to restore methanogenesis and maintain full methanol degradation coupled to methane production during more than 35 days after the CoCl2 pulse. Similar to CoCl2, pulse addition of vitamin B12 supplies enough cobalt to maintain full methanol degradation during more than 35 days after the pulse. However, the specific methanogenic activities (SMAs) of the sludge in the vitamin B12 supplied reactor were around 3 times higher than the SMA of the sludge from the CoCl2 supplied reactor at the same sampling times. An appropriate dosing strategy (repeated pulse dosing) combined with the choice of vitamin B12 as the cobalt species is suggested as a promising dosing strategy for methanol-fed anaerobic bioreactors limited by the micronutrient cobalt. © 2010 Elsevier Ltd. All rights reserved.

Black and green pigments based on chromium-cobalt spinels

Energy Technology Data Exchange (ETDEWEB)

Eliziario, Sayonara A., E-mail: sayonaraea@iq.unesp.br [Departamento de Fisico-Quimica, Instituto de Quimica, UNESP - Univ Estadual Paulista, Araraquara, SP (Brazil); Departamento de Quimica, CCEN, Universidade Federal da Paraiba, Campus I, Joao Pessoa, PB (Brazil); Andrade, Jeferson M. de [Departamento de Quimica, CCEN, Universidade Federal da Paraiba, Campus I, Joao Pessoa, PB (Brazil); Lima, Severino J.G. [Departamento de Engenharia Mecanica, CT, Universidade Federal da Paraiba, Campus I, Joao Pessoa, PB (Brazil); Paskocimas, Carlos A. [Universidade Federal do Rio Grande do Norte, CT, Natal, RN (Brazil); Soledade, Luiz E.B. [Departamento de Quimica, CCEN, Universidade Federal da Paraiba, Campus I, Joao Pessoa, PB (Brazil); Hammer, P.; Longo, E. [Departamento de Fisico-Quimica, Instituto de Quimica, UNESP - Univ Estadual Paulista, Araraquara, SP (Brazil); Souza, Antonio G.; Santos, Ieda M.G. [Departamento de Quimica, CCEN, Universidade Federal da Paraiba, Campus I, Joao Pessoa, PB (Brazil)

2011-09-15

Highlights: {yields} Co(Co{sub 2-x}Cr{sub x})O{sub 4} powders with different chromium concentrations (x = 0, 0.25 and 1) were prepared by the polymeric precursor method. {yields} Co(CoCr)O{sub 4} and Co(Co{sub 1.75}Cr{sub 0.25})O{sub 4} displayed a dark color and CoCr{sub 2}O{sub 4} was green. {yields} The colors were related to the different oxidation states of Cr and Co. {yields} Cobalt enrichment result in an increasing presence of Co(III) and a decrease amount of Cr(VI). - Abstract: Chromium and cobalt oxides are widely used in the manufacture of industrial pigments. In this work, the Co(Co{sub 2-x}Cr{sub x})O{sub 4} powders with different chromium concentrations (x = 0, 0.25 and 1) were synthesized by the polymeric precursor method, heat treatment between 600 and 1000 deg. C. These powders were characterized by X-ray diffraction, infrared spectroscopy, colorimetry, UV-vis absorption and X-ray photoelectron spectroscopies. Even with the addition of chromium, the XRD patterns revealed that all powders crystallize in a single spinel cubic structure. The spinels with higher cobalt amount, Co(CoCr)O{sub 4} and Co(Co{sub 1.75}Cr{sub 0.25})O{sub 4}, displayed a dark color, without the Co{sup 3+} reduction observed in Co{sub 3}O{sub 4} between 900 and 950 deg. C. The spinel with higher chromium amount, CoCr{sub 2}O{sub 4}, was green. The colors were directly related to the occupation of tetrahedral and octahedral sites by the chromophores, as well as to the different oxidation states of chromium and cobalt. The different optical band gap values estimated from UV-vis spectra suggested the existence of intermediary energy levels within the band gap. X-ray photoelectron spectroscopy confirmed an increasing presence of Co(III) and a decreasing amount of Cr(VI) with cobalt enrichment.

Composition tunable cobalt–nickel and cobalt–iron alloy nanoparticles below 10 nm synthesized using acetonated cobalt carbonyl

International Nuclear Information System (INIS)

Schooneveld, Matti M. van; Campos-Cuerva, Carlos; Pet, Jeroen; Meeldijk, Johannes D.; Rijssel, Jos van; Meijerink, Andries; Erné, Ben H.; Groot, Frank M. F. de

2012-01-01

A general organometallic route has been developed to synthesize Co x Ni 1−x and Co x Fe 1−x alloy nanoparticles with a fully tunable composition and a size of 4–10 nm with high yield. In contrast to previously reported synthesis methods using dicobalt octacarbonyl (Co 2 (CO) 8 ), here the cobalt–cobalt bond in the carbonyl complex is first broken with anhydrous acetone. The acetonated compound, in the presence of iron carbonyl or nickel acetylacetonate, is necessary to obtain small composition tunable alloys. This new route and insights will provide guidelines for the wet-chemical synthesis of yet unmade bimetallic alloy nanoparticles.

Unprecedented Hexanuclear Cobalt(II Nonsymmetrical Salamo-Based Coordination Compound: Synthesis, Crystal Structure, and Photophysical Properties

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Zong-Li Ren

2018-03-01

Full Text Available A novel hexanuclear Co(II coordination compound with a nonsymmetrical Salamo-type bisoxime ligandH4L, namely [{Co3(HL(MeO(MeOH2(OAc2}2]·2MeOH, was prepared and characterized by elemental analyses, UV–vis, IR and fluorescence spectra, and X-ray single-crystal diffraction analysis. Each Co(II is hexacoordinated, and possesses a distorted CoO6 or CoO4N2 octahedrons. The Co(II coordination compound possesses a self-assembled infinite 2D supramolecular structure with the help of the intermolecular C–H···O interactions. Meanwhile, the photophysical properties of the Co(II coordination compound were studied.

Influences of the matrix effect in the sensibility of cobalt measurement by atomic absorption

International Nuclear Information System (INIS)

Avila, L.A. d'.

1977-06-01

The interferences caused by iron, aluminium, calcium, magnesium, manganese, copper, nickel, zinc, sodium and potassium in the determination of cobalt by atomic absorption, were studied. The concentrations of cobalt were varied in the range of 1 to 800 μg/ml and the concentrations of the interferents in the proportions occuring normally in soils, rocks, sediments, geological material in general, alloys, caustic liquors etc. To study the flame composition effect, the flame region effect and also the effect of different interferent concentrations on the cobalt for each selected spectral line, an air-acetilene flame was utilized. As an application of this study the effect was shown of 'simulated soil matrices' with respect to the interference of iron on cobalt [pt

Reductive-sulfurizing smelting treatment of smelter slag for copper and cobalt recovery

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Li Y.

2018-01-01

Full Text Available Recovery of copper and cobalt from smelter slag using reductive-sulfurizing smelting method was performed in this study. The effects of reductive agent (coke, sulfurizing agent (pyrite, slag modifier (CaO and smelting temperature and duration on the extractive efficiencies of Cu, Co and Fe were discussed. The phase compositions and microstructure of the materials, copper-cobalt matte and cleaned slag were determined. The results showed that copper and cobalt contents in cleaned slag could decrease averagely to 0.18% and 0.071% respectively after cleaning. 91.99% Cu and 92.94% Co and less than 38.73% Fe were recovered from the smelter slag under the optimum conditions: 6 wt.% coke, 20 wt.% pyrite and 6 wt.% CaO addition to the smelter slag, smelting temperature of 1350°C and smelting duration of 3h. The addition of CaO can increase the selectivity of Co recovery. The cleaning products were characterized by XRD and SEM-EDS analysis. The results showed that the main phases of copper-cobalt matte were iron sulfide (FeS, geerite (Cu8S5, iron cobalt sulfide (Fe0.92Co0.08S and Fe-Cu-Co alloy. The cleaned slag mainly comprised fayalite (Fe2SiO4, hedenbergite (CaFe(Si2O6 and magnetite (Fe3O4.

Cobalt-Catalyzed C(sp(2))-H Borylation: Mechanistic Insights Inspire Catalyst Design.

Science.gov (United States)

Obligacion, Jennifer V; Semproni, Scott P; Pappas, Iraklis; Chirik, Paul J

2016-08-24

A comprehensive study into the mechanism of bis(phosphino)pyridine (PNP) cobalt-catalyzed C-H borylation of 2,6-lutidine using B2Pin2 (Pin = pinacolate) has been conducted. The experimentally observed rate law, deuterium kinetic isotope effects, and identification of the catalyst resting state support turnover limiting C-H activation from a fully characterized cobalt(I) boryl intermediate. Monitoring the catalytic reaction as a function of time revealed that borylation of the 4-position of the pincer in the cobalt catalyst was faster than arene borylation. Cyclic voltammetry established the electron withdrawing influence of 4-BPin, which slows the rate of C-H oxidative addition and hence overall catalytic turnover. This mechanistic insight inspired the next generation of 4-substituted PNP cobalt catalysts with electron donating and sterically blocking methyl and pyrrolidinyl substituents that exhibited increased activity for the C-H borylation of unactivated arenes. The rationally designed catalysts promote effective turnover with stoichiometric quantities of arene substrate and B2Pin2. Kinetic studies on the improved catalyst, 4-(H)2BPin, established a change in turnover limiting step from C-H oxidative addition to C-B reductive elimination. The iridium congener of the optimized cobalt catalyst, 6-(H)2BPin, was prepared and crystallographically characterized and proved inactive for C-H borylation, a result of the high kinetic barrier for reductive elimination from octahedral Ir(III) complexes.

Fatal Cobalt Toxicity after a Non-Metal-on-Metal Total Hip Arthroplasty

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Rinne M. Peters

2017-01-01

Full Text Available This case illustrates the potential for systemic cobalt toxicity in non-metal-on-metal bearings and its potentially devastating consequences. We present a 71-year-old male with grinding sensations in his right hip following ceramic-on-ceramic total hip arthroplasty (THA. After diagnosing a fractured ceramic liner, the hip prosthesis was revised into a metal-on-polyethylene bearing. At one year postoperatively, X-rays and MARS-MRI showed a fixed reversed hybrid THA, with periarticular densities, flattening of the femoral head component, and a pattern of periarticular metal wear debris and pseudotumor formation. Before revision could take place, the patient was admitted with the clinical picture of systemic cobalt toxicity, supported by excessively high serum cobalt and chromium levels, and ultimately died. At autopsy dilated cardiomyopathy as cause of death was hypothesized. A third body wear reaction between ceramic remnants and the metal femoral head very likely led to excessive metal wear, which contributed systemic cobalt toxicity leading to neurotoxicity and heart failure. This case emphasizes that fractured ceramic-on-ceramic bearings should be revised to ceramic-on-ceramic or ceramic-on-polyethylene bearings, but not to metal-on-polyethylene bearings. We aim to increase awareness among orthopedic surgeons for clinical clues for systemic cobalt intoxication, even when there is no metal-on-metal bearing surface.

Structural modifications under reactive atmosphere of cobalt catalysts; Modifications structurales sous atmospheres reactionnelles de catalyseurs a base de cobalt

Energy Technology Data Exchange (ETDEWEB)

Ducreux, O.

1999-11-23

The purpose of this work was to develop in situ methods under reactive dynamic conditions (XRD and Fourier transform infrared spectroscopy) to describe the active phase structure in order to understand Fischer-Tropsch catalyst behaviour and improve the natural gas conversion process performance. Experiments were designed to correlate structural modifications with catalytic results. The effect of ruthenium used as a promoter has also been studied. The impregnation process increases cobalt-support interaction. The presence of ruthenium promoter reduces this effect. Interactions between Co{sub 3}O{sub 4} oxide and support play an important role in the reducibility of cobalt and in the resulting metal structure. This in turn strongly influences the catalytic behaviour. Our results show a close correlation between structure modification and reactivity in the systems studied. Cobalt metal and CO can react to form a carbide Co{sub 2}C under conditions close to those of the Fischer-Tropsch synthesis. This carbide formation seems to be related to a deactivation process. The presence of interstitial carbon formed by dissociation of CO is proposed as a key to understanding the mechanism of the Fischer-Tropsch reaction. A specific catalyst activation treatment was developed to increase the catalytic activity. This work permits correlation of materials structure with their chemical properties and demonstrates the contribution of in situ physico-chemical characterisation methods to describe solids under reactive atmosphere. (author)

An analysis of cobalt irradiation in CANDU 6 reactor core

International Nuclear Information System (INIS)

Gugiu, E.D.; Dumitrache, I.

2003-01-01

In CANDU reactors, one has the ability to replace the stainless steel adjuster rods with neutronically equivalent Co assemblies with a minimum impact on the power plant safety and efficiency. The 60 Co produced by 59 Co irradiation is used extensively in medicine and industry. The paper mainly describes some of the reactor physics and safety requirements that must be carried into practice for the Co adjuster rods. The computations related to the neutronically equivalence of the stainless steel adjusters with the Co adjuster assemblies, as well as the estimations of the activity and the heating of the irradiated cobalt rods are performed using the Monte Carlo codes MCNP5 and MONTEBURNS2.1. The 60 Co activity and heating evaluations are closely related to the neutronics computations and to the density evolution of cobalt isotopes during assumed in-core irradiation period. Unfortunately, the activities of these isotopes could not be evaluated directly using the burn-up capabilities of the MONTEBURNS code because of the lack of their neutron cross-section from the MCNP5 code library. Additional MCNP5 runs for all the cobalt assemblies have been done in order to compute the flux-spectrum, the 59 Co and the 60 Co radiative capture reaction rates in the adjusters. The 60m Co cross-section was estimated using the flux-spectrum and the ORIGEN2.1 code capabilities THERM and RES. These computational steps allowed the evaluation of the one-group cross-section for the radiative capture reactions of cobalt isotopes. The values obtained replaced the corresponding ones from the ORIGEN library, which have been estimated using the flux-spectrum specific to the fuel. The activity values are used to evaluate the dose at the surface of the device designed to transport the cobalt adjusters. (authors)

Synthesis of cobalt stearate as oxidant additive for oxo-biodegradable polyethylene

Energy Technology Data Exchange (ETDEWEB)

Asriza, Ristika O.; Arcana, I Made, E-mail: arcana@chem.itb.ac.id [Division of Inorganic and Physical Chemistry, Institut Teknologi Bandung, Jl. Ganesha No. 10, Bandung, 40132 (Indonesia)

2015-09-30

Cobalt stearate is an oxidant additives that can initiate a process of degradation in high density polyethylene (HDPE). To determine the effect of cobalt stearate in HDPE, oxo-biodegradable polyethylene film was given an irradiation with UV light or heating at various temperature. After given a heating, the FTIR spectra showed a new absorption peak at wave number 1712 cm{sup −1} indicating the presence of carbonyl groups in polymers, whereas after irradiation with UV light is not visible the presence of this absorption peak. The increase concentration of cobalt stearate added in HDPE and the higher heating temperature, the intensity of the absorption peak of the carbonyl group increased. The increasing intensity of the carbonyl group absorption is caused the presence of damage in the film surface after heating, and this result is supported by analysis the surface properties of the film with using SEM. Biodegradation tests were performed on oxo-biodegradable polyethylene film which has been given heating or UV light with using activated sludge under optimal conditions the growth of microorganisms. After biodegradation, the maximum weight decreased by 23% in the oxo-biodegradable polyethylene film with a cobalt stearate concentration of 0.2% and after heating at a temperature of 75 °C for 10 days, and only 0.69% in the same film after irradiation UV light for 10 days. Based on the results above, cobalt stearate additive is more effective to initiate the oxidative degradation of HDPE when it is initiated by heating compared to irradiation with UV light.

Synthesis of cobalt stearate as oxidant additive for oxo-biodegradable polyethylene

Science.gov (United States)

Asriza, Ristika O.; Arcana, I. Made

2015-09-01

Cobalt stearate is an oxidant additives that can initiate a process of degradation in high density polyethylene (HDPE). To determine the effect of cobalt stearate in HDPE, oxo-biodegradable polyethylene film was given an irradiation with UV light or heating at various temperature. After given a heating, the FTIR spectra showed a new absorption peak at wave number 1712 cm-1 indicating the presence of carbonyl groups in polymers, whereas after irradiation with UV light is not visible the presence of this absorption peak. The increase concentration of cobalt stearate added in HDPE and the higher heating temperature, the intensity of the absorption peak of the carbonyl group increased. The increasing intensity of the carbonyl group absorption is caused the presence of damage in the film surface after heating, and this result is supported by analysis the surface properties of the film with using SEM. Biodegradation tests were performed on oxo-biodegradable polyethylene film which has been given heating or UV light with using activated sludge under optimal conditions the growth of microorganisms. After biodegradation, the maximum weight decreased by 23% in the oxo-biodegradable polyethylene film with a cobalt stearate concentration of 0.2% and after heating at a temperature of 75 °C for 10 days, and only 0.69% in the same film after irradiation UV light for 10 days. Based on the results above, cobalt stearate additive is more effective to initiate the oxidative degradation of HDPE when it is initiated by heating compared to irradiation with UV light.

Sorption of cobalt in zeolites and natural clays of the clinoptilolite and kaolinite type

International Nuclear Information System (INIS)

Davila R, J.I.; Solache R, M.

2006-01-01

In this work the sorption of cobalt of aqueous solutions in two natural zeolites (clinoptilolite) and a clay (kaolinite) of origin in the center-north region of Mexico is evaluated. The effect of the pH and the time of contact in the process of sorption were evaluated. The cobalt retained in the aluminosilicates was determined by neutron activation analysis. The cobalt sorption in the materials in a range of pH from 4 to 7 does not present significant variations. The studies of reaction kinetics show a very fast sorption in the first 5 hours of contact, reaching the equilibrium in approximately 24 hours. The kinetics of sorption of the cobalt ions was represented better by the Ritchie reaction model modified of second order. The experimental data for the zeolites obtained at ambient temperature and varying the concentration were adjusted to the models of Freundlich, Langmuir and Freundlich-Langmuir isotherms and it was observed that the cobalt sorption it behaves according to the Freundlich isotherm model. (Author)

Development of a Cloud-Point Extraction Method for Cobalt Determination in Natural Water Samples

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Mohammad Reza Jamali

2013-01-01

Full Text Available A new, simple, and versatile cloud-point extraction (CPE methodology has been developed for the separation and preconcentration of cobalt. The cobalt ions in the initial aqueous solution were complexed with 4-Benzylpiperidinedithiocarbamate, and Triton X-114 was added as surfactant. Dilution of the surfactant-rich phase with acidified ethanol was performed after phase separation, and the cobalt content was measured by flame atomic absorption spectrometry. The main factors affecting CPE procedure, such as pH, concentration of ligand, amount of Triton X-114, equilibrium temperature, and incubation time were investigated and optimized. Under the optimal conditions, the limit of detection (LOD for cobalt was 0.5 μg L-1, with sensitivity enhancement factor (EF of 67. Calibration curve was linear in the range of 2–150 μg L-1, and relative standard deviation was 3.2% (c=100 μg L-1; n=10. The proposed method was applied to the determination of trace cobalt in real water samples with satisfactory analytical results.

Assessment of polyphase sintered iron-cobalt-iron boride cermets

International Nuclear Information System (INIS)

Nowacki, J.; Pieczonka, T.

2004-01-01

Sintering of iron, cobalt and boron powders has been analysed. As a result iron-iron boride, Fe-Fe 2 B and iron/cobalt boride with a slight admixture of molybdenum, Fe - Co - (FeMoCo) 2 B cermets have been produced. Iron was introduced to the mixture as the Astalloy Mo Hoeganaes grade powder. Elemental amorphous boron powder was used, and formation of borides occurred both during heating and isothermal sintering periods causing dimensional changes of the sintered body. Dilatometry was chosen to control basic phenomena taking place during multiphase sintering of investigated systems. The microstructure and phase constituents of sintered compacts were controlled as well. The cermets produced were substituted to: metallographic tests, X-ray analysis, measurements of hardness and of microhardness, and of wear in the process of sliding dry friction. Cermets are made up of two phases; hard grains of iron - cobalt boride, (FeCo) 2 B (1800 HV) constituting the reinforcement and a relatively soft and plastic eutectic mixture Fe 2 B - Co (400-500 HV) constituting the matrix. (author)

Water splitting: Taking cobalt in isolation

Science.gov (United States)

Wang, Aiqin; Zhang, Tao

2016-01-01

The sustainable production of hydrogen is key to the delivery of clean energy in a hydrogen economy; however, lower-cost alternatives to platinum electrocatalysts are needed. Now, isolated, earth-abundant cobalt atoms dispersed over nitrogen-doped graphene are shown to efficiently electrolyse water to generate hydrogen.

Creep-fatigue of low cobalt superalloys

Science.gov (United States)

Halford, G. R.

1982-01-01

Testing for the low cycle fatigue and creep fatigue resistance of superalloys containing reduced amounts of cobalt is described. The test matrix employed involves a single high temperature appropriate for each alloy. A single total strain range, again appropriate to each alloy, is used in conducting strain controlled, low cycle, creep fatigue tests. The total strain range is based upon the level of straining that results in about 10,000 cycles to failure in a high frequency (0.5 Hz) continuous strain-cycling fatigue test. No creep is expected to occur in such a test. To bracket the influence of creep on the cyclic strain resistance, strain hold time tests with ore minute hold periods are introduced. One test per composition is conducted with the hold period in tension only, one in compression only, and one in both tension and compression. The test temperatures, alloys, and their cobalt compositions that are under study are given.

Synthesis of cobalt alloy through smelting method and its characterization as prosthesis bone implant

International Nuclear Information System (INIS)

Aminatun,; Putri, N.S Efinda; Indriani, Arista; Himawati, Umi; Hikmawati, Dyah; Suhariningsih

2014-01-01

Cobalt-based alloys are widely used as total hip and knee replacements because of their excellent properties, such as corrosion resistance, fatigue strength and biocompatibility. In this work, cobalt alloys with variation of Cr (28.5; 30; 31.5; 33, and 34.5% wt) have been synthesized by smelting method began with the process of compaction, followed by smelting process using Tri Arc Melting Furnace at 200A. Continued by homogenization process at recrystallization temperature (1250° C) for 3 hours to allow the atoms diffuses and transform into γ phase. The next process is rolling process which is accompanied by heating at 1200° C for ± 15 minutes and followed by quenching. This process is repeated until the obtained thickness of ± 1 mm. The evaluated material properties included microstructure, surface morphology, and hardness value. It was shown that microstructure of cobalt alloys with variation of Cr is dominant by γ phase, thus making the entire cobalt alloys have high hardness. It was also shown from the surface morphology of entire cobalt alloys sample indicated the whole process of synthesis that had good solubility were at flat surface area. Hardness value test showed all of cobalt alloys sample had high hardness, just variation of 33% Cr be in the range of ASTMF75, it were 345,24 VHN which is potential to be applied as an implant prosthesis

Synthesis and characterization of mixtures of cobalt and titanium oxides by mechanical alloyed and Sol-Gel;Sintesis y caracterizacion de mezclas de oxidos de cobalto y titanio por aleado mecanico y Sol-Gel

Energy Technology Data Exchange (ETDEWEB)

Basurto S, R.; Bonifacio M, J.; Fernandez V, S. M., E-mail: rafael.basurto@inin.gob.m [ININ, Departamento de Quimica, Carretera Mexico-Toluca s/n, Ocoyoacac 52750, Estado de Mexico (Mexico)

2009-07-01

The mechanical alloyed techniques continued by combustion and Sol-Gel method, were used for the synthesis of CoTiO{sub 3}. With the first technique was used Co{sub 3}O{sub 4} obtained in a balls mill SPEX in argon atmosphere, using cobalt nitrate and urea, the combustion is realized at 400 and 500 C, the characterization by X-ray diffraction showed the obtaining of the valence oxide mixed of cobalt with crystallite size from 10 to 12.5 nm and the particle size of 60 to 75 nm was obtained by scanning electron microscopy. To prepare the CoTiO{sub 3}, the obtained Co{sub 3}O{sub 4} was mixed with TiO{sub 2} on a relationship in weight (1:1) and with a milling time of 2.5 h and the combustion at 800 C. the mixed oxide of titanium cobalt was also obtained by the Sol-Gel technique starting from cobalt chloride and titanium propoxide in acetic-water acid, the gel is burned to temperature of 300, 500, 700 and 900 C, finding that this last temperature it is that provides the compound with crystalline size from 50 to 75 nm. (Author)

National Low-Level Waste Management Program Radionuclide Report Series: Volume 12, Cobalt-60

International Nuclear Information System (INIS)

Adams, J.P.

1995-06-01

This report outlines the basic radiological and chemical characteristics of cobalt-60 ( 60 Co) and examines how these characteristics affect the behavior of 60 Co in various environmental media, such as soils, groundwater, plants, animals, the atmosphere, and the human body. Discussions also include methods of 60 Co production, waste types, and waste forms that contain 60 Co. All cobalt atoms contain 27 protons (Z = 27) and various numbers of neutrons (typically N = 27 to 37 neutrons) within the atom's nucleus. There is only one stable isotope of cobalt, namely 59 Co. All other cobalt isotopes, including 60 Co, are radioactive. The radioactive isotopes of cobalt have half-lives ranging from less than a second ( 54 Co-0.19 s) to 5.2 years ( 60 Co). The radioactive isotopes of cobalt are not a normal constituent of the natural environment and are generated as a result of human activities. The primary source of 60 Co in the environment has been low-level radioactive waste material generated as a result of neutron activation of stable 59 Co that is present in the structural components of nuclear reactor vessels. This isotope is also intentionally produced, usually in reactors but also to some degree in accelerators for industrial and medical uses, such as for radiation sources for cancer treatment and nondestructive testing of metals and welds. 60 Co may enter the environment as a result of the activities associated with nuclear reactor operations and decommissioning and when industrial and medical sources are being used, manufactured, or disposed

Synthesis, multi-nonlinear dielectric resonance and electromagnetic absorption properties of hcp-cobalt particles

International Nuclear Information System (INIS)

Wen, Shulai; Liu, Ying; Zhao, Xiuchen; Cheng, Jingwei; Li, Hong

2014-01-01

Hcp-cobalt particles were successfully prepared by a liquid phase reduction method, and the microstructure, static magnetic properties, electromagnetic and microwave absorption properties of the cobalt particles with irregular shape were investigated in detail. The measured results indicate that the saturation magnetization was less than that of hcp-Co single crystals, and the coercivity was larger than that of bulk cobalt crystal. The permittivity presents multi-nonlinear dielectric resonance, which may result from the irregular shape containing parts of cutting angle of dodecahedron of cobalt particles. The real part of permeability decreases with the frequency, and the imaginary part has a wide resonant peak. The paraffin-based composite containing 70 wt% cobalt particles possessed strong absorption characteristics with a minimum RL of −38.97 dB at 10.81 GHz and an absorption band with RL under −10 dB from 8.72 to 13.26 GHz when the thickness is 1.8 mm, which exhibits excellent microwave absorption in middle and high frequency. The architectural design of material morphologies is important for improving microwave absorption properties toward future application. - Highlights: • Hcp-cobalt particles were prepared by a liquid phase reduction method. • The saturation magnetization was less than that of hcp-Co single crystals. • The permittivity presents multi-nonlinear dielectric resonance. • The real part of permeability decreases with frequency, and the imaginary part presents a wide resonant peak. • The paraffin-based composite possessed a minimum RL of −38.97 dB at 10.81 GHz

Precipitation and ion floatation of molybdenum, tungsten, copper, and cobalt compounds by cetyltrimethylammonium bromide and sodium diethyldithiocarbamate

International Nuclear Information System (INIS)

Strizhko, V.S.; Shekhirev, D.V.; Ignatkina, V.A.; Alimova, R.Eh.

1996-01-01

Experimental data are presented on application of ion-flotation in purification of low-concentration (less than 10 -3 M) acid solutions from molybdenum, tungsten, copper and cobalt ions. Two collectors, i.e. DEDC and CTMAB have been tested, their optimal consumption is determined. It is shown that CTMAB provides for selective purification from Mo and W ions and allows foam product with little water on flotation in a column to be obtained. But the achieved residual W and Mo concentration of 20 to 10 mg/l require deeper finishing purification in order to meet a sanitary permissible limiting concentration value employing other methods. DEDC provides for sufficient purification from nonferrous metal ions but does not possess selectivity with respect to some metals. The obtained results have shown the possibility to apply ion-flotation in concentration of metal ions in foam product in the process of waste water purification with further finishing purification up to a sanitary permissible limiting concentration value. 14 refs.; 3 figs.; 1 tab

Iron, lead, and cobalt absorption: similarities and dissimilarities

International Nuclear Information System (INIS)

Barton, J.C.; Conrad, M.E.; Holland, R.

1981-01-01

Using isolated intestinal segments in rats, the absorption of iron, lead, and cobalt was increased in iron deficiency and decreased in iron loading. Similarly, the absorption of these metals was decreased in transfusional erythocytosis, after intravenous iron injection and after parenteral endotoxin injection. Acute bleeding or abbreviated intervals of dietary iron deprivation resulted in increased iron absorption from isolated intestinal segments and in intact animals, while the absorption of lead and cobalt was unaffected. These results suggest that the specificity of the mucosal metal absorptive mechanism is either selectively enhanced for iron absorption by phlebotomy or brief periods of dietary iron deprivation, or that two or more mucosal pathways for iron absorption may exist

Association of coordination compounds of cobalt and molybdenum in solution

Energy Technology Data Exchange (ETDEWEB)

Kudryavtsev, A.B.; Sapunov, V.N. (Moskovskij Lesotekhnicheskij Inst. (USSR))

1981-01-01

Association of acetylacetonates Co(2) and MoO/sub 2/(6) in CHCl/sub 3/ is studied using the PMR method. In the absence of hydroxyl-containing substances the compounds form labile complex with the bond through molybdenyl oxygen. Equilibrium constant at 23 deg is equal to 2.2+-0.6 l/mol. Alcohol introduction results in partial dischelating of MoO/sub 2/(Acac)/sub 2/ and formation of mixed acetylacetonate-alcoholate complex of molybdenyl. Equilibrium constant of the reaction at 23 deg constitutes 0.14+-0.02 l/mol. Under the conditions Co(2) acetylacetonate is introduced into the first coordination sphere of MoO/sub 2/, the splitting off of the second acetylacetonate ligand and formation of strong associate which might condition the decrease of catalytic activity of mixed cobaltmolybdenum catalysts of epoxidation.

Investigation of the production of cobalt-60 via particle accelerator

Directory of Open Access Journals (Sweden)

Artun Ozan

2017-01-01

Full Text Available The production process of cobalt-60 was simulated by a particle accelerator in the energy range of 5 to 100 MeV, particle beam current of 1 mA, and irradiation time of 1 hour to perform yield, activity of reaction, and integral yield for charged particle-induced reactions. Based on nuclear reaction processes, the obtained results in the production process of cobalt-60 were also discussed in detail to determine appropriate target material, optimum energy ranges, and suitable reactions.

The substitution of nickel for cobalt in hot isostatically pressed powder metallurgy UDIMET 700 alloys

Science.gov (United States)

Harf, F. H.

1985-01-01

Nickel was substituted in various proportions for cobalt in a series of five hot-isostatically-pressed powder metallurgy alloys based on the UDIMET 700 composition. These alloys were given 5-step heat treatments appropriate for use in turbine engine disks. The resultant microstructures displayed three distinct sizes of gamma-prime particles in a gamma matrix. The higher cobalt-content alloys contained larger amounts of the finest gamma-prime particles, and had the lowest gamma-gamma-prime lattice mismatch. While all alloys had approximately the same tensile properties at 25 and 650 gamma C, the rupture lives at 650 and 760 C peaked in the alloys with cobalt contents between 12.7 and 4.3 pct. Minimum creep rates increased as cobalt contents were lowered, suggesting their correlation with the gamma-prime particle size distribution and the gamma-gamma-prime mismatch. It was also found that, on overaging at temperatures higher than suitable for turbine disk use, the high cobalt-content alloys were prone to sigma phase formation.

Sorption of cobalt and nickel on anaerobic granular sludges: isotherms and sequential extraction

NARCIS (Netherlands)

Hullebusch, van E.D.; Peerbolte, A.; Zandvoort, M.H.; Lens, P.N.L.

2005-01-01

The objective of this study was to investigate the sorption capacity and the fractionation of sorbed nickel and cobalt onto anaerobic granular sludges. Two different anaerobic granular sludges (non-fed, pH = 7) were loaded with nickel and cobalt in. adsorption experiments (monometal and competitive

Changes in the vascular tissue of fresh Hass avocados treated with cobalt

International Nuclear Information System (INIS)

Arevalo, Lourdes; Bustos, Ma. Emilia; Saucedo, Cresenciano

2002-01-01

This research was based on fresh avocado fruit treated with gamma rays at quarantine doses and stored at room temperature. The effects of irradiation were analyzed and measured by three different types of studies: histological, biochemical and physiological. Histological studies were focused on the effect of Cobalt 60 gamma rays in the mesocarp of avocado irradiated at three different doses; 150, 250, and 350 Gy. Damage was observed principally in the parenchyma tissue where the cell membrane was plazmolized and a red color was observed due to the development of phenol compounds. Another important effect was an increase in the size of xylem and phloem cells in the vascular tissue even at the minimum dose of 150 Gy. The biochemical and the physiological studies were done on avocado fruit irradiated at 100 and 150 Gy. An increase in L-phenilalanine ammonialyase activity was observed and therefore, an increase in the concentration of phenol compounds. These changes were not perceived by panelists in a sensorial test. Irradiated fruits were accepted by panelists as well as control fruit as regards parameters of taste, internal color and external color. These results demonstrate the feasibility of using irradiation to disinfest avocado fruit using a minimum dose of 100 Gy

Changes in the vascular tissue of fresh Hass avocados treated with cobalt

Energy Technology Data Exchange (ETDEWEB)

Arevalo, Lourdes; Bustos, Ma. Emilia; Saucedo, Cresenciano

2002-03-01

This research was based on fresh avocado fruit treated with gamma rays at quarantine doses and stored at room temperature. The effects of irradiation were analyzed and measured by three different types of studies: histological, biochemical and physiological. Histological studies were focused on the effect of Cobalt 60 gamma rays in the mesocarp of avocado irradiated at three different doses; 150, 250, and 350 Gy. Damage was observed principally in the parenchyma tissue where the cell membrane was plazmolized and a red color was observed due to the development of phenol compounds. Another important effect was an increase in the size of xylem and phloem cells in the vascular tissue even at the minimum dose of 150 Gy. The biochemical and the physiological studies were done on avocado fruit irradiated at 100 and 150 Gy. An increase in L-phenilalanine ammonialyase activity was observed and therefore, an increase in the concentration of phenol compounds. These changes were not perceived by panelists in a sensorial test. Irradiated fruits were accepted by panelists as well as control fruit as regards parameters of taste, internal color and external color. These results demonstrate the feasibility of using irradiation to disinfest avocado fruit using a minimum dose of 100 Gy.

Anion-Regulated Selective Generation of Cobalt Sites in Carbon: Toward Superior Bifunctional Electrocatalysis

Energy Technology Data Exchange (ETDEWEB)

Wan, Gang [State Key Laboratory of High Performance Ceramics and Superfine Microstructures, Shanghai Institute of Ceramics, Chinese Academy of Sciences, 1295 Ding-xi Road Shanghai 200050 P. R. China; University of Chinese Academy of Sciences, Beijing 100049 P. R. China; Yang, Ce [Chemical Science and Engineering Division, Argonne National Laboratory, 9700 Cass Avenue Lemont IL 60439 USA; Zhao, Wanpeng [State Key Laboratory of High Performance Ceramics and Superfine Microstructures, Shanghai Institute of Ceramics, Chinese Academy of Sciences, 1295 Ding-xi Road Shanghai 200050 P. R. China; University of Chinese Academy of Sciences, Beijing 100049 P. R. China; Li, Qianru [State Key Laboratory of High Performance Ceramics and Superfine Microstructures, Shanghai Institute of Ceramics, Chinese Academy of Sciences, 1295 Ding-xi Road Shanghai 200050 P. R. China; University of Chinese Academy of Sciences, Beijing 100049 P. R. China; Wang, Ning [State Key Laboratory of High Performance Ceramics and Superfine Microstructures, Shanghai Institute of Ceramics, Chinese Academy of Sciences, 1295 Ding-xi Road Shanghai 200050 P. R. China; University of Chinese Academy of Sciences, Beijing 100049 P. R. China; Li, Tao [X-ray Science Division, Advanced Photon Source, Argonne National Laboratory, 9700 Cass Avenue Lemont IL 60439 USA; Zhou, Hua [X-ray Science Division, Advanced Photon Source, Argonne National Laboratory, 9700 Cass Avenue Lemont IL 60439 USA; Chen, Hangrong [State Key Laboratory of High Performance Ceramics and Superfine Microstructures, Shanghai Institute of Ceramics, Chinese Academy of Sciences, 1295 Ding-xi Road Shanghai 200050 P. R. China; Shi, Jianlin [State Key Laboratory of High Performance Ceramics and Superfine Microstructures, Shanghai Institute of Ceramics, Chinese Academy of Sciences, 1295 Ding-xi Road Shanghai 200050 P. R. China

2017-11-06

The introduction of active transition metal sites (TMSs) in carbon enables the synthesis of noble-metal-free electrocatalysts for clean energy conversion applications, however, there are often multiple existing forms of TMSs, which are of different natures and catalytic models. Regulating the evolution of distinctive TMSs is highly desirable but remains challenging to date. Anions, as essential elements involved in the synthesis, have been totally neglected previously in the construction of TMSs. Herein, the effects of anions on the creation of different types of TMSs is investigated for the first time. It is found that the active cobalt-nitrogen sites tend to be selectively constructed on the surface of N-doped carbon by using chloride, while metallic cobalt nanoparticles encased in protective graphite layers are the dominant forms of cobalt species with nitrate ions. The obtained catalysts demonstrate cobalt-sites-dependent activity for ORR and HER in acidic media. And the remarkably enhanced catalytic activities approaching that of benchmark Pt/C in acidic medium has been obtained on the catalyst dominated with cobalt-nitrogen sites, confirmed by the advanced spectroscopic . Our finding demonstrates a general paradigm of anion-regulated evolution of distinctive TMSs, providing a new pathway for enhancing performances of various targeted reactions related with TMSs.

Recovery of cobalt from spent lithium-ion batteries using supercritical carbon dioxide extraction.

Science.gov (United States)

Bertuol, Daniel A; Machado, Caroline M; Silva, Mariana L; Calgaro, Camila O; Dotto, Guilherme L; Tanabe, Eduardo H

2016-05-01

Continuing technological development decreases the useful lifetime of electronic equipment, resulting in the generation of waste and the need for new and more efficient recycling processes. The objective of this work is to study the effectiveness of supercritical fluids for the leaching of cobalt contained in lithium-ion batteries (LIBs). For comparative purposes, leaching tests are performed with supercritical CO2 and co-solvents, as well as under conventional conditions. In both cases, sulfuric acid and H2O2 are used as reagents. The solution obtained from the supercritical leaching is processed using electrowinning in order to recover the cobalt. The results show that at atmospheric pressure, cobalt leaching is favored by increasing the amount of H2O2 (from 0 to 8% v/v). The use of supercritical conditions enable extraction of more than 95wt% of the cobalt, with reduction of the reaction time from 60min (the time employed in leaching at atmospheric pressure) to 5min, and a reduction in the concentration of H2O2 required from 8 to 4% (v/v). Electrowinning using a leach solution achieve a current efficiency of 96% and a deposit with cobalt concentration of 99.5wt%. Copyright © 2016 Elsevier Ltd. All rights reserved.

Cobalt products from real waste fractions of end of life lithium ion batteries.

Science.gov (United States)

Pagnanelli, Francesca; Moscardini, Emanuela; Altimari, Pietro; Abo Atia, Thomas; Toro, Luigi

2016-05-01

An innovative process was optimized to recover Co from portable Lithium Ion Batteries (LIB). Pilot scale physical pretreatment was performed to recover electrodic powder from LIB. Co was extracted from electrodic powder by a hydrometallurgical process including the following main stages: leaching (by acid reducing conditions), primary purification (by precipitation of metal impurities), solvent extraction with D2EPHA (for removal of metal impurities), solvent extraction with Cyanex 272 (for separation of cobalt from nickel), cobalt recovery (by precipitation of cobalt carbonate). Tests were separately performed to identify the optimal operating conditions for precipitation (pH 3.8 or 4.8), solvent extraction with D2EHPA (pH 3.8; Mn/D2EHPA=4; 10% TBP; two sequential extractive steps) and solvent extraction with Cyanex 272 (pH 3.8; Cyanex/Cobalt=4, 10% TBP, one extractive step). The sequence of optimized process stages was finally performed to obtain cobalt carbonate. Products with different degree of purity were obtained depending on the performed purification steps (precipitation with or without solvent extraction). 95% purity was achieved by implementation of the process including the solvent extraction stages with D2EHPA and Cyanex 272 and final washing for sodium removal. Copyright © 2016 Elsevier Ltd. All rights reserved.

Characterization of Cobalt F-75 powder for biomedical application

International Nuclear Information System (INIS)

Zuraidawani, C.D.; Shamsul, J.B.; Fazlul, B.; Nur Hidayah, A.Z.

2007-01-01

Cobalt F-75 alloys is commonly used for surgical implants because of their strength, corrosion resistance, non-magnetic behaviour and biocompatibility. In this paper, gas atomized of Cobalt F-75 powders were selected for evaluation. These powders supplied by Sandvik Osprey Ltd. The characteristics of these powders were investigated by using particle size analysis, X-ray Diffraction (XRD), X-ray Fluorescence (XRF) and Scanning Electron Microscope (SEM). Two different powder sizes (8.8 μm and 11.5 μm) have showed spherical morphology and the value of densities are 7.9 and 7.6 g/cm 3 respectively. (author)

Diagnostic Value of the Cobalt (58Co) Excretion Test in Iron Deficiency Anemia

International Nuclear Information System (INIS)

Sihn, Hyun Chung; Hong, Kee Suck; Cho, Kyung Sam; Song, In Kyung; Koh, Chang Soon; Lee, Mun Ho

1976-01-01

The diagnosis of iron deficiency rests upon the correct evaluation of body iron stores. Morphological interpretation of blood film and the red cell indices are not reliable and often absent in mild iron deficiency. Serum iron levels and iron-binding capacity are more sensitive indices of iron deficiency, but they are often normal in iron depletion and mild iron deficiency anemia. They are also subject ro many variables which may introduce substantial errors and influenced by many pathologic and physiologic states. Examination of the bone marrow aspirate for stainable iron has been regarded as one of the most sensitive and reliable diagnostic method for detecting iron deficiency, but this also has limitations. Thus, there is still need for a more practical, but sensitive and reliable substitute as a screening test of iron deficiency. Pollack et al. (1965) observed that the intestinal absorption of cobalt was raised in iron, deficient rats and Valberg et al. (1969) found that cobalt absorption was elevated in patients with iron deficiency. A direct correlation was demonstrated between the amounts of radioiron and radiocobalt absorbed. Unlike iron, excess cobalt was excreted by the kidney, the percentage of radioactivity in the urine being directly related to the percentage absorbed from the gastro-intestinal tract. Recently a test based on the urinary excretion of an oral dose of 57 Co has been proposed as a method for detecting iron deficiency. To assess the diagnostic value of urinary cobalt excretion test cobaltous chloride labelled with 1 μCi of 58 Co was given by mouth and the percentage of the test dose excreted in the urine was measured by a gamma counter. The mean 24 hour urinary cobalt excretion in control subjects with normal iron stores was 6.1%(1.9-15.2%). Cobalt excretion was markedly increased in patients with iron deficiency and excreted more than 29% of the dose. In contrast, patients with anemia due to causes other than iron deficiency excreted less

Removal of Cobalt ion by Foam Flotation(I)

Energy Technology Data Exchange (ETDEWEB)

Jung, I.H.; Park, H.S.; Moon, J.S.; Yim, S.P.; Bae, K.K. [Korea Atomic Energy Research Institute (Korea)

1999-02-01

Simulated liquid waste containing 50 ppm cobalt ion was treated by precipitate flotation using the surfactant of sodium lauryl sulfate. The effects of initial cobalt ion concentration, pH, surfactant concentration, removal time, gas flow rate and foreign ions were estimated on removal efficiency. 35% H{sub 2}O{sub 2} was added for pre-treatment stage before precipitate flotation. As the result of pre-treatment, optimum removal pH and the pH of treated water being discharged were lowed and optimum removal pH range was broadened. For the result of this experiment, 99.8% removal efficiency was obtained at the condition of 50ppm of initial cobalt ion concentration, pH 9.5, 70 mL/min of gas flow rate, and 30 min of removal time. Attraction between precipitate and surfactant was supposed to be influenced by solubility and chemical affinity among species in solution as well as zeta potential. The influence of foreign ions such as, NO{sub 3}{sup -}, SO{sub 4}{sup -2}, Na{sup +}, Ca{sup +2} on the removal efficiency was also observed. Removal efficiency by precipitate flotation containing o.1 M of SO4{sup -}2 ion decreased to 90% due to the decrease of zeta potential and interruption of precipitation. 12 refs., 8 figs.

Cobalt60 plaques in recurrent retinoblastoma

Energy Technology Data Exchange (ETDEWEB)

Fass, D.; McCormick, B.; Abramson, D.; Ellsworth, R. (Department of Radiation Oncology, Memorial Sloan-Kettering Cancer Center, NY, NY (USA))

1991-08-01

Cobalt60 plaque irradiation is one treatment option for patients with recurrent retinoblastoma following conventional external beam irradiation (ERT). Tumorocidal doses can be delivered without excessive risk of normal tissue injury. In patients not considered candidates for xenon arc or cryotherapy, 60Co is an alternative to enucleation. Between 1968 and 1987, 85 patients were treated with 60Co plaques, 72 of whom had failed prior ERT. Age at diagnosis ranged from 1 week to 4 years. There are 37 males and 35 females. Seventy-one patients had bilateral disease and one had unilateral. Three patients had both eyes plaqued. Prior ERT ranged from 30 to 70 Gy (mean 4200 Gy). Time from initial therapy to failure ranged from 13 to 60 months. Cobalt plaques of 10 mm, 15 mm, or 10 {times} 15 mm were used depending on tumor size and location. Dose prescribed to the apex of the tumor ranged from 30 to 50 Gy (median 40 Gy) given over 3 to 8 days. Twelve patients had two plaque applications; three patients had three plaque applications. All patients were followed with routine ophthalmoscopic examinations. Follow-up ranged from 2 to 22 years (mean 8.7). Seven patients died of metastatic disease; 10 patients developed non-ocular second tumors. Thirty patients required enucleation. Twenty-two patients had clear tumor progression, two patients had radiation complications, and six patients had a combination of tumor growth and complications. Cobalt60 can salvage eyes in retinoblastoma patients failing ERT. Currently, the authors are using I125 in an attempt to spare normal ocular tissue and reduce subsequent complications.

Cobalt60 plaques in recurrent retinoblastoma

International Nuclear Information System (INIS)

Fass, D.; McCormick, B.; Abramson, D.; Ellsworth, R.

1991-01-01

Cobalt60 plaque irradiation is one treatment option for patients with recurrent retinoblastoma following conventional external beam irradiation (ERT). Tumorocidal doses can be delivered without excessive risk of normal tissue injury. In patients not considered candidates for xenon arc or cryotherapy, 60Co is an alternative to enucleation. Between 1968 and 1987, 85 patients were treated with 60Co plaques, 72 of whom had failed prior ERT. Age at diagnosis ranged from 1 week to 4 years. There are 37 males and 35 females. Seventy-one patients had bilateral disease and one had unilateral. Three patients had both eyes plaqued. Prior ERT ranged from 30 to 70 Gy (mean 4200 Gy). Time from initial therapy to failure ranged from 13 to 60 months. Cobalt plaques of 10 mm, 15 mm, or 10 x 15 mm were used depending on tumor size and location. Dose prescribed to the apex of the tumor ranged from 30 to 50 Gy (median 40 Gy) given over 3 to 8 days. Twelve patients had two plaque applications; three patients had three plaque applications. All patients were followed with routine ophthalmoscopic examinations. Follow-up ranged from 2 to 22 years (mean 8.7). Seven patients died of metastatic disease; 10 patients developed non-ocular second tumors. Thirty patients required enucleation. Twenty-two patients had clear tumor progression, two patients had radiation complications, and six patients had a combination of tumor growth and complications. Cobalt60 can salvage eyes in retinoblastoma patients failing ERT. Currently, the authors are using I125 in an attempt to spare normal ocular tissue and reduce subsequent complications

Structural variation study of cobalt nanoparticles synthesized by co-precipitation method using 59Co NMR

Science.gov (United States)

Manjunatha, M.; Kumar, Rajeev; B. M., Siddesh; Sahoo, Balaram; Damle, R.; Ramesh, K. P.

2018-04-01

We have synthesized cobalt nanoparticles using co-precipitation method. Further, the two phases of the cobalt is monitored by varying the synthesis parameters. 59Co NMR and XRD are used as characterization tools to study the phase variation in the cobalt samples. XRD and NMR results show a remarkable correlation in the two samples (Co-1 and Co-2). Co-2 has predominant fcc and hcp phases, whereas, Co-1 has fcc phase with lower amount of hcp. Both the samples show same saturation magnetization (Ms) but there is a remarkable difference in the phase composition. Thus, 59Co NMR appears to be a good tool to identify the phase purity of the ferromagnetic cobalt samples.

Tuning size and catalytic activity of nano-clusters of cobalt oxide

Indian Academy of Sciences (India)

Unknown

oxalic acid, (2) co-precipitating cobalt nitrate with sodium carbonate, and (3) using sodium dodecyl sul- .... Co(NO3)2 + Na2CO3 → CoCO3 + 2NaNO3,. CoCO3. ∆. → ∆ CoO + CO2,. CoO → (in air and heating) Co3O4. In method III, cobalt nitrate, sodium dodecyl sul- .... The conversion of cyclohexane on the current po-.

Effects of bathing on skin exposed to Cobalt-60 teletherapy

International Nuclear Information System (INIS)

Bohannan, P.A.

1982-01-01

The problem of this study was to determine the effects of bathing or not bathing on the degree of skin reaction occurring in patients receiving Cobalt-60 radiation therapy to the chest, back, or head and neck. A quasi experimental study was done using a 2 x 7 repeated measures design. Sixty-seven subjects receiving Cobalt-60 radiation therapy at the Moncrief Radiation Center in Fort Worth, Texas, were randomly assigned to an experimental group who did not bathe during therapy and a control group who did bathe with water during therapy. Observations were made after each 1000 rads of therapy and two weeks after the final treatment. Erythema and pigmentation measurements were taken using the Photovolt 670 and rates were assigned using the Baker-Leith Rating Scale. Findings from the study suggest that bathing the portal of entry with water during the treatment period does not influence the degree of skin response that occurs from Cobalt-60 teletherapy

Edge reactivity and water-assisted dissociation on cobalt oxide nanoislands

International Nuclear Information System (INIS)

Fester, J.; García-Melchor, M.; Walton, A. S.; Bajdich, M.

2017-01-01

Here, transition metal oxides show great promise as Earth-abundant catalysts for the oxygen evolution reaction in electrochemical water splitting. However, progress in the development of highly active oxide nanostructures is hampered by a lack of knowledge of the location and nature of the active sites. Here we show, through atom-resolved scanning tunnelling microscopy, X-ray spectroscopy and computational modelling, how hydroxyls form from water dissociation at under coordinated cobalt edge sites of cobalt oxide nanoislands. Surprisingly, we find that an additional water molecule acts to promote all the elementary steps of the dissociation process and subsequent hydrogen migration, revealing the important assisting role of a water molecule in its own dissociation process on a metal oxide. Inspired by the experimental findings, we theoretically model the oxygen evolution reaction activity of cobalt oxide nanoislands and show that the nanoparticle metal edges also display favourable adsorption energetics for water oxidation under electrochemical conditions.

Study of thermodynamic properties of binary and ternary liquid alloys of aluminium with the elements iron, cobalt, nickel and oxygen; Etude des proprietes thermodynamiques des alliages liquides binaires et ternaires de l'aluminium avec les elements fer, cobalt, nickel et l'oxygene

Energy Technology Data Exchange (ETDEWEB)

Vachet, F [CEA Vallee du Rhone, 26-Pierrelatte (France)

1966-07-01

The present work deals with the thermodynamic study of aluminium liquid alloys with the metals iron, cobalt and nickel. The experiments carried out lead to the activity, at 1600 deg C, of aluminium in the (Al, Fe), (Al, Co), (Al, Ni) liquid alloys. The experimental method used consists in studying the partition of aluminium between the liquid immiscible phases made up with the pairs of metals (Fe, Ag), (Co, Ag), (Ni, Ag). The informations so obtained are used for drawing the isothermal equilibrium phases diagrams sections of (Al, Fe, Ag), (Al, Co, Ag), (Al, Ni, Ag) systems. The study of the partition of silver between lead and aluminium joined with the determinations of several authors allows us to determine the aluminium activity, analytically presented, in the metal M (iron cobalt and nickel). The Wagner's interaction parameters of aluminium in metal M are determined. The results obtained as the equilibrium phases diagrams of (Al, M) systems allow to compare the thermodynamic properties of the Al Fe system in liquid and solid states and to estimate the enthalpies of melting of the AlCo and AlNi intermetallic compounds. The activity, at 1600 deg C, of aluminium in (Al, Fe, Co), (Al, Fe, Ni), (Al, Co, Ni) liquid alloys is estimated through thermodynamic properties of binary components systems by application of several methods leading to results in good agreement. The study of aluminium-oxygen interactions in the liquid metallic solvants M allows us to propose an explanation for the shape of the deoxidation equilibrium line of iron, cobalt and nickel by aluminium and to compare the de-oxidizing power of aluminium toward iron, cobalt and nickel oxides. (author) [French] Le travail presente se rapporte a l'etude thermodynamique des alliages liquides de l'aluminium avec les metaux fer, cobalt et nickel. Les experiences effectuees ont pour but de determiner l'activite, a 1600 C, de l'aluminium dans les alliages liquides (Al, Fe), (Al, Co), (Al, Ni). La methode

Cobalt nanoparticles as recyclable catalyst for aerobic oxidation of alcohols in liquid phase

Energy Technology Data Exchange (ETDEWEB)

Mondal, Arijit; Mukherjee, Debkumar, E-mail: debkumarmukherjee@rediffmail.com [Ramsaday College, Department of Chemistry (India); Adhikary, Bibhutosh, E-mail: adhikarybibhu@yahoo.com [Indian Institute of Engineering, Sciences and Technology, Shibpur, Department of Chemistry (India); Ahmed, Md Azharuddin [University of Calcutta, Department of Physics (India)

2016-05-15

Cobalt nanoparticles prepared at room temperature from cobalt sulphate and tetrabutyl ammonium bromide as surfactant have been found to be effective oxidation catalysts. Palladium and platinum nanoparticles (average size 4–6 nm) can also be prepared from PdCl{sub 2} and K{sub 2}PtCl{sub 4}, respectively, using the same surfactant but require high temperature (~120 °C) and much longer preparation time. Agglomeration of nanoparticles prepared from metals like palladium and platinum in common solvents, however, restricts their use as catalysts. It is therefore our endeavour to find the right combination of catalyst and solvent that will be beneficial from industrial point of view. Magnetic property measurement of cobalt nanoclusters was made using SQUID to identify their reusability nature. Herein, we report the use of cobalt nanoparticles (average size 90–95 nm) in dichloromethane solvent as effective reusable catalysts for aerobic oxidation of a variety of alcohols.Graphical Abstract.

Effects of metallic nanoparticle doped flux on the interfacial intermetallic compounds between lead-free solder ball and copper substrate

International Nuclear Information System (INIS)