Cobalt materials

The cobalt deposition rate on new, replacement, or decontaminated recirculation piping surface has been reduced by pretreating the piping using an atmosphere of oxygenated wet steam to form an oxide film (25). Studies have been conducted for both PWRs and BWRs to reduce the cobalt content of materials used in the nuclear parts of the plants, particularly in hardened and wear surfaces where cobalt-base alloys ( 50% Co) are used (26). Some low cobalt materials have been developed however, the use of the materials is limited to replacement parts or new plants. 

K. Halbach 1980, (Design of permanent multipole magnets with oriented rare earth cobalt material), Nud. Instrum. Meth. 169, 1-10. 

XPS results are very similar. The Co 2p splitting values 15.5 0.1 eV are equal within experimental error, the N(amine)/Co atomic ratios are 1.7 and 1.3, respectively, and the individual Co/Mn surface and bulk ratios are approximately equal at each pH. This latter result indicates that the sorption process occurs predominately on the surface at pH 6 and 7. The Co 2p splitting results are intermediate between values measured for Co(III) and Co(II)-containing compounds. To account for the Co 2p splitting result, a cobalt material with such an intermediate splitting or a mixture of the two cobalt oxidation states must be present. A survey of representative cobalt-containing materials (19,24,26) reveals that Co 2p splittings at about 15.5 eV are not common. 

Special carbide tools also will often contain various percentages of titanium, tantalum, niobium icolumbium). and hafnium carbides, along witii die tungsten carbide. Chromium and vanadium carbides are also added to produce special, fine-grain-size grades of cemented tungsten carbide-cobalt materials. See Fig. 1. 

K. Minura et al., Preparation of high-purity cobalt . Materials Science and Engineering, A334(2002), 127-133... 

When considering the applicability of one or of several of the above-mentioned measures, one has to distinguish between two completely different situations. The first is when a new plant is to be designed and constructed the second relates to plants which have already been in operation for a shorter or longer period of time. In the first-mentioned case, the most effective way certainly is the proper selection of the materials to be used, in order to reduce the cobalt inventory of the primary circuit as far as possible in particular, the high-cobalt materials inside the reactor pressure vessel should be dropped in favor of substitute alloys of equal quality. In the second case, on the other hand, replacement of such materials is only rarely feasible (e. g. in the course of a replacement of components), so that other measures have to be taken into account. 

Halbach, K. (1980). Design of Permanent Multipole Magnets with Oriented Rare Earth Cobalt Material . Nuclear Instruments and Methods 169 (1) 1-10. 

COBALT AND COBALT ALLOYS] O/ol 6) [DENTAL MATERIALS] (Vol7)... 

Butane-Naphtha Catalytic Liquid-Phase Oxidation. Direct Hquid-phase oxidation ofbutane and/or naphtha [8030-30-6] was once the most favored worldwide route to acetic acid because of the low cost of these hydrocarbons. Butane [106-97-8] in the presence of metallic ions, eg, cobalt, chromium, or manganese, undergoes simple air oxidation in acetic acid solvent (48). The peroxidic intermediates are decomposed by high temperature, by mechanical agitation, and by action of the metallic catalysts, to form acetic acid and a comparatively small suite of other compounds (49). Ethyl acetate and butanone are produced, and the process can be altered to provide larger quantities of these valuable materials. Ethanol is thought to be an important intermediate (50) acetone forms through a minor pathway from isobutane present in the hydrocarbon feed. Formic acid, propionic acid, and minor quantities of butyric acid are also formed. 

Protein-Based Adhesives. Proteia-based adhesives are aormaHy used as stmctural adhesives they are all polyamino acids that are derived from blood, fish skin, caseia [9000-71 -9] soybeans, or animal hides, bones, and connective tissue (coUagen). Setting or cross-linking methods typically used are iasolubilization by means of hydrated lime and denaturation. Denaturation methods require energy which can come from heat, pressure, or radiation, as well as chemical denaturants such as carbon disulfide [75-15-0] or thiourea [62-56-6]. Complexiag salts such as those based upon cobalt, copper, or chromium have also been used. Formaldehyde and formaldehyde donors such as h exam ethyl en etetra am in e can be used to form cross-links. Removal of water from a proteia will also often denature the material. 

Cobalt difluoride, used primarily for the manufacture of cobalt trifluoride, CoF, is available from Advance Research Chemicals, Inc., Aldrich Chemicals, and PCR in the United States, Fluorochem in the UK, and Schuhardt in Germany. The 1993 price varied from 60 to 200/kg depending on the quantity and the price of cobalt metal. C0F2 is shipped as a corrosive and toxic material in DOT-approved containers. 

The ACGIH adopted TLV/TWA for 1992—1993 for fluorides as F is TWA 2.5 mg/m, and for cobalt as Co metal dust TWA 0.05 mg/m. Dust masks should be used while handling both the cobalt fluorides and all other cobalt compounds. CoF is shipped as an oxidizer and a corrosive material. 

Many perfluoroaUphatic ethers and tertiary amines have been prepared by electrochemical fluorination (1 6), direct fluorination using elemental fluorine (7—9), or, in a few cases, by fluorination using cobalt trifluoride (10). Examples of lower molecular weight materials are shown in Table 1. In addition to these, there are three commercial classes of perfluoropolyethers prepared by anionic polymerization of hexafluoropropene oxide [428-59-1] (11,12), photooxidation of hexafluoropropene [116-15-4] or tetrafluoroethene [116-14-3] (13,14), or by anionic ring-opening polymeriza tion of tetrafluorooxetane [765-63-9] followed by direct fluorination (15). 

Advanced composites and fiber-reinforced materials are used in sailcloth, speedboat, and other types of boat components, and leisure and commercial fishing gear. A ram id and polyethylene fibers are currentiy used in conveyer belts to collect valuable offshore minerals such as cobalt, uranium, and manganese. Constmction of oil-adsorbing fences made of high performance fabrics is being evaluated in Japan as well as the constmction of other pollution control textile materials for maritime use. For most marine uses, the textile materials must be resistant to biodeterioration and to a variety of aqueous pollutants and environmental conditions. 

Appllca.tlons. The principal appHcations of nickel-base superalloys are in gas turbines, where they are utilized as blades, disks, and sheet metal parts. Abcraft gas turbines utilized in both commercial and military service depend upon superalloys for parts exposed to peak metal temperatures in excess of 1000°C. Typical gas turbine engines produced in the United States in 1990 utilized nickel and cobalt-base superalloys for 46% of total engine weight (41). However, programs for future aerospace propulsion systems emphasize the need for lightweight materials having greater heat resistance. For such apphcations, intermetallics matrix composites and ceramic composites are expected to be needed. 

Cobalt aHoys may find appHcation ia a fluidized-bed process for the direct combustion of coal (qv). CoCrAlY-coated Haynes 188 has proven to be one of the most resistant materials to a fireside corrosion process encountered ia tubes coimected the fluidized-bed combustor to a steam turbiae. 

A more extensive comparison of many potential turbine blade materials is available (67). The refractory metals and a ceramic, sHicon nitride, provide a much higher value of 100 h stress—mpture life, normalised by density, than any of the cobalt- or nickel-base aHoys. Several intermetaHics and intermetaUic matrix composites, eg, aHoyed Nb Al and MoSi —SiC composites, also show very high creep resistance at 1100°C (68). Nevertheless, the superaHoys are expected to continue to dominate high temperature aHoy technology for some time. 

The second reaction is called the Fischer-Tropsch synthesis of hydrocarbons. Depending on the conditions and catalysts, a wide range of hydrocarbons from very light materials up to heavy waxes can be produced. Catalysts for the Fischer-Tropsch reaction iaclude iron, cobalt, nickel, and mthenium. Reaction temperatures range from about 150 to 350°C reaction pressures range from 0.1 to tens of MPa (1 to several hundred atm) (77). The Fischer-Tropsch process was developed iadustriaHy under the designation of the Synthol process by the M. W. Kellogg Co. from 1940 to 1960 (83). 

Nickel and cobalt are recovered by processes that employ both pressure leaching and precipitation steps. The raw materials for these processes can be sulfide concentrates, matte, arsenide concentrates, and precipitated sulfides. Typically, acidic conditions are used for leaching however, ammonia is also effective in leach solutions because of the tendency for soluble cobalt and nickel ammines to form under the leach conditions. 

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