Gotowe bibliografie tematyczne / Cobalt

Gotowa bibliografia na temat „Cobalt”

Autor: Grafiati
Data publikacji: 4 czerwca 2021
Data aktualizacji: 29 lipca 2024

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Artykuły w czasopismach na temat "Cobalt"

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Catalani, S., MC Rizzetti, A. Padovani i P. Apostoli. "Neurotoxicity of cobalt". Human & Experimental Toxicology 31, nr 5 (5.07.2011): 421–37. http://dx.doi.org/10.1177/0960327111414280.

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Cobalt exerts well-known and documented toxic effects on the thyroid, heart and the haematopoietic system, in addition to the occupational lung disease, allergic manifestations and a probably carcinogenic action. Cobalt neurotoxicity is reported in isolated cases, and it has never been systematically treated. Bilateral optic atrophy and retinopathy, bilateral nerve deafness and sensory-motor polyneuropathy have been described long ago as a result of chronic occupational exposure to cobal powder or during long-term treatment of anaemia with cobalt chloride. Recently, some patients with high levels of cobalt released from metal prosthesis have been referred as presenting with tinnitus, deafness, vertigo, visual changes, optic atrophy, tremor and peripheral neuropathy. The aim of this work is to group these cases and to identify a possible mechanism of cobalt neurotoxicity, focusing on hypothetic individual susceptibility such as altered metal-binding proteins, altered transport processes in target cells or polymorphic variation of genetic background.
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Ved, Marina, Nikolay Sakhnenko, Marina Glushkova i Tetiana Bairachna. "Electrodeposition of Functional Cobalt-Silver and Cobalt-Tungstean Alloys". Chemistry & Chemical Technology 8, nr 3 (1.09.2014): 275–81. http://dx.doi.org/10.23939/chcht08.03.275.

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Juzikis, P., L. Gudavičiūtŧ i E. Matulionis. "Ruthenium-Cobalt Alloy Electrodeposition". Platinum Metals Review 39, nr 2 (1.04.1995): 68–71. http://dx.doi.org/10.1595/003214095x3926871.

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Since little has been written about ruthenium alloy plating, the present work sets out to provide data on the electrodeposition of ruthenium-cobalt alloys, using a sulphate-sulphamate electrolyte. Some operating conditions have been obtained for the production of thin crack-free coatings of ruthenium-cobult alloys.
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Yusifova, N. V., A. M. Pashajanov, N. I. Ismailov i T. M. Ismailov. "SOLVENT EXTRACTION OF COBALT FROM LEACHING SOLUTIONS OF COBALT ORES". Azerbaijan Chemical Journal, nr 2 (19.06.2023): 178–85. http://dx.doi.org/10.32737/0005-2531-2023-2-178-185.

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The extraction of cobalt with amines has been studied in the most detail. The article presents experimental data obtained in the study of cobalt extraction from leaching solutions of cobalt ores with a mixture of tributylamine (TBA) in toluene and hexane. The dependence of the extraction degree and distribution coefficient of cobalt on pH, time, and the ratio of aqueous and organic phases have been studied. It has been shown that cobalt is maximally extracted with TBA in toluene in the pH range of 3-5 for no more than 5-10 minutes; in this case, 98% of cobalt extraction is achieved. The developed method of cobalt extraction with organic extractants can be widely used in non-ferrous metallurgy
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Rosert, R. "Cobalt-based alloys for surfacing". Paton Welding Journal 2015, nr 6 (28.06.2015): 101–6. http://dx.doi.org/10.15407/tpwj2015.06.23.

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Harwell, David E., Juliet Nabakka, Carolyn B. Knobler i M. Frederick Hawthorne. "Synthesis and structural characterization of an ether-bridged cobalta-bis(dicarbollide): a model for Venus flytrap cluster reagents". Canadian Journal of Chemistry 73, nr 7 (1.07.1995): 1044–49. http://dx.doi.org/10.1139/v95-129.

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The synthesis of bis-(1-carboranylmethyl) ether was first published in 1963; however, its subsequent complexation with a transition metal was never reported. We now report the complexation of cobalt and the corresponding X-ray structure for the triphenylmethylphosphonium salt of the cobalta-bis(carboranylmethyl) ether. The cobalt complex crystallized in the monoclinic space group C2/c with a = 21.729(6) Å, b = 9.845(2) Å, c = 35.565(9) Å, β = 105.363(9)°, V = 7336 Å3, and Z = 8. Data were collected using CuKα radiation, to a maximum 2θ = 115°, giving 4123 unique reflections, and the structure was solved by heavy atom methods. The final discrepancy index was R = 0.093, Rw = 0.100 for 1919 independent reflections with I > 3σ(I). This metala-bis(carboranylalkyl) ether is the first in a new class of Venus flytrap compounds (VFC), containing an ether linkage, to be synthesized as model compounds for the development of reagents suitable for use in the radioimmunodetection and radioimmunotherapy of cancer. Keywords: cobalt, radioimmunodetection, radioimmunotherapy, Venus flytrap.
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Wadepohl, Hubert, Wolfgang Galm, Hans Pritzkow i Andreas Wolf. "Cyclopentadienyl Cobalt Complexes of Cobalta-pentalenes: Products Formed by Reaction of (?-Cyclopentadienylidene) Cobalt Complexes with Silylalkynes". Angewandte Chemie International Edition in English 31, nr 8 (sierpień 1992): 1058–60. http://dx.doi.org/10.1002/anie.199210581.

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McLaren, R. G., D. M. Lawson, R. S. Swift i D. Purves. "The effects of cobalt additions on soil and herbage cobalt concentrations in some S.E. Scotland pastures". Journal of Agricultural Science 105, nr 2 (październik 1985): 347–63. http://dx.doi.org/10.1017/s0021859600056409.

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SUMMARYCobalt, as cobalt sulphate and cobalt-EDTA, was applied to pastures at 15 sites in south-east Scotland. Herbage cobalt and extractable soil cobalt concentrations were monitored at these sites over the period 1978–81. Although the sites were located in a generally cobalt-deficient area, considerable variation between sites was observed both in the concentration of cobalt present in untreated pasture and in the response to cobalt additions. There was no significant correlation between herbage cobalt concentrations and soil cobalt status as determined by acetic acid extraction. Application of cobalt sulphate (6 kg/ha) increased herbage cobalt concentrations at all sites but at several sites the response was short-lived. In general, cobalt-EDTA was less effective than cobalt sulphate in increasing herbage cobalt concentrations.Extractable soil cobalt concentrations of the control areas showed some variability between samplings, but the variability was much greater for the cobalt-treated plots. Cobalt applied to pastures was found to accumulate in the top 0–4 cm layer of soil and penetrated deeper only in soils of low pH. Overall, only a third of the cobalt applied to pastures as cobalt sulphate was recovered by acetic acid extraction of the soil and less than 20% of the cobalt applied as cobalt-EDTA.
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Underwood, Eric J. "Cobalt". Nutrition Reviews 33, nr 3 (27.04.2009): 65–69. http://dx.doi.org/10.1111/j.1753-4887.1975.tb06019.x.

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SCHWAB, EKKEHARD. "COBALT". Chemical & Engineering News 81, nr 36 (8.09.2003): 80. http://dx.doi.org/10.1021/cen-v081n036.p080.

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Rozprawy doktorskie na temat "Cobalt"

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England, Craig Dennis. "Properties of cobalt/copper and cobalt/palladium multilayers". Diss., The University of Arizona, 1991. http://hdl.handle.net/10150/185707.

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The physical properties of Co/Cu and Co/Pd magnetic multilayers have been studied. The Co/Cu multilayers were prepared by sputtering, while the Co/Pd multilayers were made by sputtering and molecular beam epitaxy (MBE). Various x-ray diffraction techniques have been used to study the structure of the multilayers. Magnetometry techniques were used to study the magnetic properties. Various optical techniques have been used to investigate the magneto-optical properties. Brillouin light scattering spectroscopy was used to determine the effective elastic constants of the Co/Cu multilayers and the magnetic properties of the sputtered Co/Pd multilayers.
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Reinikainen, Matti. "Cobalt and ruthenium-cobalt catalysts in CO hydrogeneration and hydroformylation /". Espoo : Technical Research Centre of Finland, 1998. http://www.vtt.fi/inf/pdf/publications/1998/P363.pdf.

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Pigram, David Dennis. "The electronic structure of the ferromagnets cobalt and cobalt disulphide". Thesis, University of Cambridge, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.306516.

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Ballou, Rafik. "Anisotropies magnétiques du cobalt dans les composés intermétalliques lanthanide-cobalt". Grenoble 1, 1987. http://www.theses.fr/1987GRE10114.

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Analyse phénoménologique des processus d'aimantation des composes YCo5 et GDCo5 mettant en évidence une anisotropie des interactions d'échangé Ln-Co liée à l'anisotropie de polarisation des électrons 5d de l'atome Ln. Etude de l'incidence de l'instabilité du magnétisme de bande 3d sur l'anisotropie magnétique dans les phases Ln2Co7 et LnCo3. Etude de l'anisotropie des systèmes à empilement quasi-unidimensionnel LnCo(1-epsilon ). Analyse de la sélection orbitale induite par les intégrales de transfert
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Ballou, Rafik. "Anisotropies magnétiques du cobalt dans les composés intermétalliques lanthanide-cobalt". Grenoble 2 : ANRT, 1987. http://catalogue.bnf.fr/ark:/12148/cb37602561f.

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Pour, Asghar Tajali. "Electrocrystallisation of cobalt". Thesis, Coventry University, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.279419.

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Grant, Simon Jonathon. "Azamacrocyclic cobalt catalysts". Thesis, University of Warwick, 1991. http://wrap.warwick.ac.uk/109401/.

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Ten azamacrocyclic ligands were synthesised and characterised. The coordination chemistry of these ligands was evaluated by the study of their Ni(II), Cu(II) and Zn(II) complexes in the development of azamacrocyclic cobalt catalysts. Co(II) complexes of ligands L3 and L4 were evaluated as potential auto-oxidation catalysts for aqueous gloss paint systems. These compounds act as catalysts, producing through dry paint films in a shorter time than commercially available catalysts. This surprising result could indicate the presence of a different drying mechanism for these complexes when compared to the commercial catalysts. Ligands L5 and L6 were designed to activate dioxygen when coordinated to Co(II). The X-ray crystal structure of [Zn(L5)](BF4)2 and n.O.e. experiments on [Zn(L6)](BF4)2 prove that the correct theoretical geometry is adopted by the ligands on coordination to metals. The Co(II) complexes of ligands L5 and L6 were not isolated as a result of their high reactivity towards dioxygen. The products obtained were the u-peroxo- bridged dimer species - a result of a bimolecular reaction. The Co(II) compounds were considered too reactive to be used as auto-oxidation catalysts. Azamacrocyclic organocobalt(III) complexes have been shown to act as photopolymerisation catalysts in the polymerisation of alkenes. In water a free radical mechanism occurs. In t.h.f. a metal centred polymerisation is proposed. Diode array gel permeation chromatography of polymeric solutions shows the presence of dimeric and trimeric species which could react to form high molecular weight species. A novel hydridocobalt(III) complex of L8 was prepared by reaction of hydrogen with [Co(L8)]2+. The presence of the Co-H bond was established by chemical means. A similar reaction was attempted for [Co(L7)](BF4)2 but the compound was unstable in solution, reductively eliminating H2-.
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Sun, Lihui. "Synthesis and reactivity of some cobalt-, phosphorus-chiral cobalt(III) complexes". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp01/MQ34235.pdf.

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Zitoun, David. "Synthèse et magnétisme de nanoparticules de cobalt/rhodium et cobalt/ruthénium". Toulouse 3, 2003. http://www.theses.fr/2003TOU30078.

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Ullman, Andrew. "Polynuclear Cobalt Complexes as Models of a Cobalt Water Oxidation Catalyst". Thesis, Harvard University, 2015. http://nrs.harvard.edu/urn-3:HUL.InstRepos:23845429.

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The electrochemical oxidation of Co2+ ions in the presence of a buffering species such as phosphate (Pi), methyl phosphonate (MePi), and borate (Bi) leads to the formation of amorphous cobalt oxide thin films that are capable of catalyzing the four electron-four proton oxidation of water to dioxygen. These cobalt oxygen evolving catalysts (Co–OECs) have been extensively studied by electrochemical techniques; however, the amorphous nature of these films means that garnering insights at the molecular and atomic level is difficult because electronic and structural characterization methods rely on measurements of bulk material. To address this challenge, polynuclear cobalt hydroxide and cobalt oxide compounds have been employed as platforms for understanding Co–OECs at the molecular level. In the first part of the thesis, we present the synthesis of a heptanuclear cobalt cluster in two different oxidation states, Co(II)7 and a mixed valence Co(III)Co(II)6. An anomalously slow self–exchange electron transfer rate as compared to that predicted from semiclassical Marcus theory was measured, supporting a charge transfer process that is accelerated by dissociation of the anion from the oxidized cluster. This mechanism sheds light on the inverse dependence of anions in the deposition mechanism of Co–OECs. Moreover, the results address a long-standing controversy surrounding the Co2+/3+ self–exchange electron transfer reaction of the hexaaqua complex. In the second part of the thesis, we report the synthesis and characterization of a dinuclear cobalt complex, which we use as an edge sites mimic (ESM) of the Co-OEC. A comparative investigation of the Pi and Bi binding of buffers to this ESM is provided. We find that the binding to the boric acid component of borate buffer is rapid, while binding to K2HPO4 is much slower, taking days to equilibrate at room temperature. These studies are used to provide a model for the interaction of Pi and Bi species with the active site of the Co-OEC. An inverse dependence on [Bi] of the electrochemical driven water oxidation activity by Co-OECs is demonstrated, which provides validation for the model and indicates that dinuclear cobalt edge sites are necessary for water oxidation catalysis. In the final chapter of the thesis, we use a series of spectroscopic and electrochemical methods to show that the observed water oxidation activity of the compound class Co4O4(OAc)4(py–X)4 emanates from a Co(II) impurity. This impurity is oxidized to produce Co-OEC, which is an active water oxidation catalyst. Differential electrochemical mass spectrometry (DEMS) is used to characterize the fate of glassy carbon at water oxidizing potentials, and demonstrate that such electrode materials should be used with caution for the study of water oxidation catalysis. We then investigate the electrochemical properties of Co4O4 cubanes in non-aqueous solvents, showing that the neutral cubanes may be oxidized by two electrons yielding a formal oxidation state of Co(IV)2Co(III)2. Finally, we show that these cubanes may be synthetically modified with tethered NMI photooxidants, which opens new avenues for exploring fixed-distance photoinduced ET using Co4O4 cubanes as the electron donor. Ultra-fast transient absorption experiments demonstrate that a charge separated state is formed following laser excitation.
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Książki na temat "Cobalt"

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Kirk, William S. Cobalt. [Washington, D.C.?]: Bureau of Mines, U.S. Dept. of the Interior, 1985.

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Aldyne, Nathan. Cobalt. Los Angeles: Alyson Publications, 1998.

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Johanson, Paula. Cobalt. New York: Rosen Pub. Group, 2008.

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Aldyne, Nathan. Cobalt. New York: Felony & Mayhem Press, 2013.

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Watt, Susan. Cobalt. New York: Marshall Cavendish Benchmark, 2007.

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United States. Agency for Toxic Substances and Disease Registry. Division of Toxicology. Cobalt. Atlanta, Ga: Dept. of Health and Human Services, Agency for Toxic Substances and Disease Registry, Division of Toxicology, 2004.

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H, Kim James, Gibb Herman J, Howe Paul D, Sheffer Marla, United Nations Environment Programme, International Labour Organisation, Inter-Organization Programme for the Sound Management of Chemicals. i World Health Organization, red. Cobalt and inorganic cobalt compounds. Geneva: World Health Organization, 2006.

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Almond, Peter R. Cobalt Blues. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-4924-9.

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Raveau, Bernard, i Md Motin Seikh. Cobalt Oxides. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527645527.

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Graves, Richard L. Cobalt 60. South Yarmouth, Ma: Curley & Associates, 1989.

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Części książek na temat "Cobalt"

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Warlimont, Hans. "Cobalt and Cobalt Alloys". W Springer Handbook of Materials Data, 271–78. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-69743-7_10.

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Bährle-Rapp, Marina. "Cobalt". W Springer Lexikon Kosmetik und Körperpflege, 120. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_2221.

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Kurtz, Wolfgang, i Hans Vanecek. "Cobalt". W W Tungsten, 173–79. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-662-08690-2_24.

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Pourret, Olivier, i Michel-Pierre Faucon. "Cobalt". W Encyclopedia of Earth Sciences Series, 1–3. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-39193-9_271-1.

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Pourret, Olivier, i Michel-Pierre Faucon. "Cobalt". W Encyclopedia of Earth Sciences Series, 1–4. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-39193-9_271-2.

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Pourret, Olivier, i Michel-Pierre Faucon. "Cobalt". W Encyclopedia of Earth Sciences Series, 291–94. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-39312-4_271.

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Crowson, Phillip. "Cobalt". W Minerals Handbook 1992–93, 69–75. London: Palgrave Macmillan UK, 1992. http://dx.doi.org/10.1007/978-1-349-12564-7_11.

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Gooch, Jan W. "Cobalt". W Encyclopedic Dictionary of Polymers, 150. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_2510.

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Singh, Davinderjit, i Raymond D. Harbison. "Cobalt". W Hamilton & Hardy's Industrial Toxicology, 101–8. Hoboken, New Jersey: John Wiley & Sons, Inc., 2015. http://dx.doi.org/10.1002/9781118834015.ch14.

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Julander, Anneli, Jolinde Kettelarij i Carola Lidén. "Cobalt". W Kanerva’s Occupational Dermatology, 1–10. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-40221-5_45-2.

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Streszczenia konferencji na temat "Cobalt"

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Ong, Michaelina, Wisley Ung, Chai Chin Chin i Seok Sewoon. "Cobalt stripping process integration for cobalt salicide residue improvement". W 2008 IEEE International Conference on Semiconductor Electronics (ICSE). IEEE, 2008. http://dx.doi.org/10.1109/smelec.2008.4770399.

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Chang, Y. M., Y. J. Hsu, T. M. Liu, H. W. Chu, Y. J. Chuo, J. G. Lin i C. H. Chen. "Magnetization-induced second-harmonic generation of cobalt and cobalt oxide nanoparticles". W Integrated Optoelectronic Devices 2006, redaktorzy Kong-Thon Tsen, Jin-Joo Song i Hongxing Jiang. SPIE, 2006. http://dx.doi.org/10.1117/12.657821.

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Fiala, Petr, i Karel Hajmrle. "Cobalt Based Antifretting Coatings". W ASME Turbo Expo 2010: Power for Land, Sea, and Air. ASMEDC, 2010. http://dx.doi.org/10.1115/gt2010-23547.

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Some cobalt based coatings have excellent antifretting properties when rubbed against titanium alloy hardware. The coatings are presently used in the gas turbine industry for specific antifretting applications. Their superior performance compared to the current art CuNiIn coatings has been demonstrated. This paper discusses the influence of coating structure on its mechanical properties and antifretting performance. The coating structure can be greatly modified by changing the coating application method (HVOF or plasma spraying). HVOF (High Velocity Oxygen-Fuel) and plasma spray equipment together with TriplexPro™ 200 gun configured to spray HVOF and plasma type coatings were used. The resulting coating properties can be tailored to specific application requirements encountered in aircraft engines and other industrial applications.
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Gryaznova, Mariya, i Elena Belaya. "Thermolysis of cobalt ferrite". W PROCEEDINGS OF INTERNATIONAL CONFERENCE ON RECENT TRENDS IN MECHANICAL AND MATERIALS ENGINEERING: ICRTMME 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0023203.

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Kingsbury, Ryan, Jon Twichell i Scott Palo. "Cobalt optical crosslink terminal". W Free-Space Laser Communications XXXIV, redaktorzy Hamid Hemmati i Bryan S. Robinson. SPIE, 2022. http://dx.doi.org/10.1117/12.2610501.

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Huang, Zi-Xun, Tin Li i Jin-Kun Jai. "Cobalt and Cobalt-Based Alusninized Duplex Diffusion Coatings for Aeroengine Hot Sections". W Annual Aerospace/Airline Plating and Metal Finishing Forum and Exposition. 400 Commonwealth Drive, Warrendale, PA, United States: SAE International, 1985. http://dx.doi.org/10.4271/850705.

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Wang, Zhipeng, Mohd Zamri Mohd Yusop, Takehiko Hihara, Yasuhiko Hayashi i Masaki Tanemura. "Fabrication of ion-induced carbon-cobalt nanocomposite fibers: Effect of cobalt supply rate". W 2010 IEEE 3rd International Nanoelectronics Conference (INEC). IEEE, 2010. http://dx.doi.org/10.1109/inec.2010.5424534.

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Bekiaris, Nikolaos, Zhiyuan Wu, He Ren, Mehul Naik, Jin Hee Park, Mark Lee, Tae Hong Ha i in. "Cobalt fill for advanced interconnects". W 2017 IEEE International Interconnect Technology Conference (IITC). IEEE, 2017. http://dx.doi.org/10.1109/iitc-amc.2017.7968981.

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Nur, Adrian, Arif Jumari, Anatta W. Budiman, Ossama Ruzicka, Maulana A. Fajri, Nazriati Nazriati i Fauziatul Fajaroh. "Electrosynthesis of cobalt – hydroxyapatite nanoparticles". W THE 4TH INTERNATIONAL CONFERENCE ON INDUSTRIAL, MECHANICAL, ELECTRICAL, AND CHEMICAL ENGINEERING. Author(s), 2019. http://dx.doi.org/10.1063/1.5098187.

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Vitt, B. "Properties Of Black Cobalt Coatings". W 31st Annual Technical Symposium, redaktor Carl M. Lampert. SPIE, 1987. http://dx.doi.org/10.1117/12.941906.

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Raporty organizacyjne na temat "Cobalt"

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Barnes, M. Cobalt Source Calibration. Office of Scientific and Technical Information (OSTI), październik 1999. http://dx.doi.org/10.2172/14271.

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Rizvi, H. M. Cobalt source calibration. Office of Scientific and Technical Information (OSTI), grudzień 1999. http://dx.doi.org/10.2172/750095.

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Cawood, T. K., i J. M. Peter. The geology of critical battery metals: a spotlight on Co in VMS deposits and Li in pegmatites. Natural Resources Canada/CMSS/Information Management, 2024. http://dx.doi.org/10.4095/332348.

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As we move away from a fossil fuel-driven economy, the demand for metals used in energy-dense, rechargeable batteries is increasing; these include cobalt and lithium. Although cobalt is mostly obtained as a by-product from nickel and copper mining, significant amounts also occur in volcanogenic massive sulfide (VMS) deposits, of which Canada has many. However, the primary controls on cobalt distribution in VMS deposits are poorly understood, and may be affected by deformation and metamorphism. We show that cobalt can occur in pyrite, which retains its primary composition through greenschist facies metamorphism; and in pyrrhotite, which expels some cobalt during deformation to form cobaltite crystals. In contrast, most of the global lithium supply is derived from rare metal pegmatites and salars, with pegmatites the most important Canadian source. Our preliminary results confirm that lithium-bearing pegmatites can form directly during anatexis, as well as from fractional crystallization of large bodies of granitic magma.
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Ruzicka, V., i R. I. Thorpe. Arsenide silver-cobalt veins. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1995. http://dx.doi.org/10.4095/207996.

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Alexander, Jake. Cobalt Database of Utah. Utah Geological Survey, maj 2023. http://dx.doi.org/10.34191/ofr-749.

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This report and accompanying database collate known cobalt mineral occurrences and geochemical data for the state of Utah. These data were compiled from the Utah Geological Survey’s Utah Mineral Occurrence System database (UMOS), the National Uranium Resource Evaluation Hydrogeochemical and Stream Sediment Reconnaissance program (NURE-HSSR; U.S. Geological Survey, 2004) geochemical database, the U.S. Geological Survey National Geochemical Database (NGDB; U.S. Geological Survey, 2016), and the Utah Geochemistry Database (UGDB; unpublished internal Utah Geological Survey database).
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Gross, Brian J. Neutronic Comparison of New HSA Cobalt Capsule Design to Legacy HSA Cobalt Capsule Design. Office of Scientific and Technical Information (OSTI), styczeń 2018. http://dx.doi.org/10.2172/1478517.

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Percival, J. B., Y. T. J. Kwong, C. G. Dumaresq i F. A. Michel. Transport and attenuation of arsenic, cobalt and nickel in an alkaline environment (Cobalt, Ontario). Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 2004. http://dx.doi.org/10.4095/214977.

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Holland, Patrick L. High-Spin Cobalt Hydrides for Catalysis. Office of Scientific and Technical Information (OSTI), sierpień 2013. http://dx.doi.org/10.2172/1091379.

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Percival, J. B., C. G. Dumaresq, Y. T. J. Kwong, K. B. Hendry i F A Michel. Arsenic in surface waters, Cobalt, Ontario. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1996. http://dx.doi.org/10.4095/207451.

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Mendolia, M. S., i G. C. Farrington. Solvation of Cobalt Salts by Oligomeric Polyethers. Fort Belvoir, VA: Defense Technical Information Center, czerwiec 1992. http://dx.doi.org/10.21236/ada254815.

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