Cobalt-iron

Copper, nickel, cobalt, iron, and zinc (270) for their physical properties using ultraviolet and infrared spectrometry (271). 

Chromium—Cobalt—Iron Alloys. In 1971, a family of ductile Cr—Co—Fe permanent-magnet alloys was developed (79). The Cr—Co—Fe alloys are analogous to the Alnicos in metallurgical stmcture and in permanent magnetic properties, but are cold formable at room temperature. Equivalent magnetic properties also can be attained with substantially less Co, thereby offering savings in materials cost. 

Vanadium—Cobalt-Iron Alloys. V—Co—Fe permanent-magnet alloys also are ductile. A common commercial ahoy, Vicahoy I, has a nominal composition 10 wt % V, 52 wt % Co, and 38 wt % Fe (Table 10). Hard magnetic properties are developed by quenching from 1200°C for conversion to bcc a-phase foUowed by aging at 600°C (precipitation of fee y-phase). The resulting properties are isotropic, with ca kJ/m ... 

Niobium carbide is used as a component of hard metals, eg, mixtures of metal carbides that are cemented with cobalt, iron, and nickel. Along with tantalum carbide, niobium carbide is added to impart toughness and shock and erosion resistance. The spiraling rise in the price of tantalum has spurred the development of a hafnium carbide—niobium carbide substitute for tantalum carbide (68). These cemented carbides are used for tool bits, drill bits, shovel teeth, and other wear-resistant components turbine blades and as dies in high pressure apparatus (see Carbides). 

Nickel—Iron and Cobalt—Iron Alloys. Selenium improves the machinabifity of Ni—Ee and Co—Ee alloys which are used for electrical appfications. Neither sulfur nor tellurium are usefiil additives because these elements cause hot britdeness. The addition of 0.4—0.5% selenium promotes a columnar crystal stmcture on solidification, doubling the coercive force of cobalt—iron-titanium alloy permanent magnets produced with an equiaxial grain stmcture. 

An acidic solvent is recommended for use with palladium. Other catalysts that have been used for this reduction include copper chromite and any of the three Raney catalysts, cobalt, iron, or nickel. 

Cesium does not alloy with or attack cobalt, iron, molybdenum, nickel, platinum, tantalum, or tungsten at temperatures up to 650°C (35). 

Cobalt—molybdenum alloys are used for the desulfurization of high sulfur bituminous coal, and cobalt—iron alloys in the hydrocracking of cmde oil shale (qv) and in coalhquefaction (6). 

Earlier catalysts were based on cobalt, iron, and nickel. However, recent catalytic systems involve rhodium compounds promoted by methyl iodide and lithium iodide (48,49). Higher mol wt alkyl esters do not show any particular abiUty to undergo carbonylation to anhydrides. 

Metal oxides, sulfides, and hydrides form a transition between acid/base and metal catalysts. They catalyze hydrogenation/dehydro-genation as well as many of the reactions catalyzed by acids, such as cracking and isomerization. Their oxidation activity is related to the possibility of two valence states which allow oxygen to be released and reabsorbed alternately. Common examples are oxides of cobalt, iron, zinc, and chromium and hydrides of precious metals that can release hydrogen readily. Sulfide catalysts are more resistant than metals to the formation of coke deposits and to poisoning by sulfur compounds their main application is in hydrodesulfurization. 

Reduction of unsaturated aldehydes seems more influenced by the catalyst than is that of unsaturated ketones, probably because of the less hindered nature of the aldehydic function. A variety of special catalysts, such as unsupported (96), or supported (SJ) platinum-iron-zinc, plalinum-nickel-iron (47), platinum-cobalt (90), nickel-cobalt-iron (42-44), osmium (<55), rhenium heptoxide (74), or iridium-on-carbon (49), have been developed for selective hydrogenation of the carbonyl group in unsaturated aldehydes. None of these catalysts appears to reduce an a,/3-unsaturated ketonic carbonyl selectively. 

The sotrace elements, such as boron, cobalt, iron,copper, zinc, manganese, chromium, molybdenum and still others may also be used to advantage. Generally, these trace elements occur in sufficient quantities in the carbonaceous and nitrogenous constituents of the medium, particularly if derived from natural sources, or in the tap water, and the addition of further quantities of these trace elements may consequently be unnecessary. 

Fischer Tropsch synthesis is catalyzed by a variety of transition metals such as iron, nickel, and cobalt. Iron is the preferred catalyst due to its higher activity and lower cost. Nickel produces large amounts of methane, while cobalt has a lower reaction rate and lower selectivity than iron. By comparing cobalt and iron catalysts, it was found that cobalt promotes more middle-distillate products. In FTS, cobalt produces... 

For the cathode seal material, there is a criterion that the thermal expansion coefficient of the metal component must be lower than that of the a-alumina header. A nickel-cobalt-iron alloy (NiloK) with a... 

Oceans occupy 70.8% or 125 million square miles of the surface of the earth. Within or beneath this inner space are foods, fuels, and minerals. Thus interest in the sea is obvious. At least 4/5 of all life on earth exists in saltwater. It is predicted that of the oil and gas demand in future years will come from oil at 2,000 ft. depths operated by manned submarines and marine robots. All the equipment needed to collect and store oil or gas will be installed and operated on the sea floor. Underwater housing and decompression chambers will be required. The sea bottom is also reported to include trillions of tons of copper, nickel, cobalt, iron, and other important minerals. 

Sample Number Molyb- denum Nickel Cobalt Iron Chro- mium Total >... 

Sample Number Molybdenum Nickel 1 Cobalt Iron Chromium ... 

Iron(II) complex of tris(N -tert-butylurea-ylato)-N-ethylene]aminato activates dioxygen at room temperature to afford an iron(III) complex containing a single terminal oxo ligand. X-ray structures show that the three urea molecules act as a tridentate N,N,N-hgand [52]. The tripodal ligand was also used to synthesise complexes of cobalt, iron or zinc with terminal hydroxo ligands (Scheme 8) [53]. 

Table I. Blank Concentrations for Dissolved Cobalt, Iron, Scandium (ng/mL) Given as Stem-and-Leaf Displays (Tukey 1977) W...

In the early work on the thermolysis of metal complexes for the synthesis of metal nanoparticles, the precursor carbonyl complex of transition metals, e.g., Co2(CO)8, in organic solvent functions as a metal source of nanoparticles and thermally decomposes in the presence of various polymers to afford polymer-protected metal nanoparticles under relatively mild conditions [1-3]. Particle sizes depend on the kind of polymers, ranging from 5 to >100 nm. The particle size distribution sometimes became wide. Other cobalt, iron [4], nickel [5], rhodium, iridium, rutheniuim, osmium, palladium, and platinum nanoparticles stabilized by polymers have been prepared by similar thermolysis procedures. Besides carbonyl complexes, palladium acetate, palladium acetylacetonate, and platinum acetylac-etonate were also used as a precursor complex in organic solvents like methyl-wo-butylketone [6-9]. These results proposed facile preparative method of metal nanoparticles. However, it may be considered that the size-regulated preparation of metal nanoparticles by thermolysis procedure should be conducted under the limited condition. 

When the temperature of a carbonate reservoir that is saturated with high-viscosity oil and water increases to 200° C or more, chemical reactions occur in the formation, resulting in the formation of considerable amounts of CO2. The generation of CO2 during thermal stimulation of a carbonate reservoir results from the dealkylation of aromatic hydrocarbons in the presence of water vapor, catalytic conversion of hydrocarbons by water vapor, and oxidation of organic materials. Clay material and metals of variable valence (e.g., nickel, cobalt, iron) in the carbonate rock can serve as the catalyst. An optimal amount of CO2 exists for which maximal oil recovery is achieved [1538]. The performance of a steamflooding process can be improved by the addition of CO2 or methane [1216]. 

When nitryl fluoride is passed at ambient temperature over molybdenum, potassium, sodium, thorium, uranium or zirconium, glowing or white incandescence occurs. Mild warming is needed to initiate similar reactions of aluminium, cadmium, cobalt, iron, nickel, titanium, tungsten, vanadium or zinc, and 200-300°C for lithium or manganese. 

Mitchell, J. A., The Electrodeposition of Cobalt, Iron, Antimony and Their Alloys from Acidic Aluminum Chloride 1 -methyl-3-ethylimidazolium Chloride Room-Temperature Molten Salts, Ph.D. Dissertation, 1997, University of Mississippi University, MS. 

FIGURE 9.7 Operating ranges of the catalysts nickel, cobalt, iron, and ruthenium in FT synthesis as indicated by Pichler. 

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