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Iron powder, manufacture

However, it is recognized that slightly soluble intermediates such as CdO(OH) and Cd(OH)3 are involved. Cadmium does not corrode since its equilibrium potential is more positive than that of hydrogen in the same solution. The active material in pocket plate cells consists of metallic cadmium, with up to 25% of iron and small quantities of nickel and graphite to prevent agglomeration. Two methods of preparation are used. One involves the electrochemical co-reduction of a solution of cadmium and iron sulphate in the other, dry mixtures of cadmium oxide or hydroxide and Fe304 or iron powder are used. In some methods of pocket plate manufacture, the electrode material is pressed into pellets or briquettes before being inserted into the pockets, and various waxes or oils may be used to facilitate this process. [Pg.164]

In pocket plate cells, the active materials are a mixture of finely powdered metallic iron and Fe304. The preparation of this mixture varies from manufacturer to manufacturer, but generally involves a final process in which controlled air oxidation of iron powder or reduction of Fe304 with hydrogen is used to form the appropriate composition. Additives such as cadmium, cadmium oxide or graphite are commonly included to improve the capacity retention and electronic conductance. The performance of the electrode is improved by the addition of up to 0.5% of FeS the mechanism of the sulphide involvement is not well understood. If sulphide is lost by oxidation after prolonged use, small amounts of soluble sulphide may be added to the electrolyte,... [Pg.188]

For applications in magnetic cores for electronic components, iron powder is manufactured by the thermal decomposition of Fe(CO)5 ... [Pg.710]

Cast-Iron-Bonded Diamond. These wheels are manufactured by mixing diamond abrasive, cast-iron powder or fibers, and a small amount of carbonyl iron powder. The compound is shaped in the desired form under a pressure of 6-8 t/cm, and then sintered in an atmosphere of ammonia. These wheels are not suited for continuous grinding for long... [Pg.209]

Iron oxides, synthetic (e.g., Fe203-H20) n. Iron oxides manufactured by a synthetic process. Kirk-Othmer encyclopedia of chemical technology pigments-powders. [Pg.537]

H2O2 can be used in conjunction with free halogens in two-step substitution reactions, being added half way through to convert the liberated HX back to halogen and thence to product. This approach is used in manufacture of tetrabromophthalic anhydride [259], a flame retardant precursor, where iodine acts as catalyst. Iron powder can also be employed. [Pg.295]

The positive active material of a pocket-type electrode consists of nickel hydroxide powder by which cobalt hydroxide was coprecipitated, and is obtained from those mixed sulfate by a neutralizing method. Graphite powder is mixed as a conductor. The addition of cobalt is performed for increasing the capacity of the positive active material. Cadmium hydroxide which is a negative active material is manufactured by a coprecipitation method or a dry-mixing method. Moreover, iron powder is usually mixed with negative active material of a pocket type electrode for the increase in capacity. Graphite powder and/or nickel flake is mixed as a conductor. [Pg.1361]

Abstract Smart composites based on carbonyl iron powder, micro and nano size Fe304 in ethylene - propylene and acrylonitrile - butadiene rubber were manufactured and studied. Elastomer samples with various volume fractions of magnetic particles were tested. To improve dispersion of applied fillers in polymer matrix, ionic liquids were added during the process of composites preparation. To align particles in elastomer, cross-linking process took place in magnetic field. [Pg.23]

The degradation of Ni(CO)4 or Fe(CO)5 to the respective metal and CO is a means of manufacturing high-purity nickel and iron. The thermal decomposition of Ni(CO)4 is used in the Mond process to refine nickel (see eq. 21.4). Iron powder for use in magnetic cores in electronic components is produced by thermally decomposing Fe(CO)5. The Fe particles act as nucleation centres for the production of particles up to 8 pm in diameter. [Pg.912]

Elastomer mixtures, based on EPM or NER filled with micro- and nano- sized iron oxides and carbonyl iron powder were prepared by common manufacturing ptrocedmes for rubber. [Pg.215]

Originally, iron powder from mill scrap was used in powder metallurgy. The soap was primarily iron oxide that would fall off the steel as it was being milled. The iron oxide dust was heated in a hydrogen atmosphere to reduee the oxide to iron particles. Manufacturers called the powdered metal iron sponge because numa-ous holes form in the particles when the oxygen escapes. [Pg.1081]

Heterogeneous vapor-phase fluorination of a chlorocarbon or chlorohydrocarbon with HP over a supported metal catalyst is an alternative to the hquid phase process. Salts of chromium, nickel, cobalt or iron on an A1P. support are considered viable catalysts in pellet or fluidized powder form. This process can be used to manufacture CPC-11 and CPC-12, but is hampered by the formation of over-fluorinated by-products with Httle to no commercial value. The most effective appHcation for vapor-phase fluorination is where all the halogens are to be replaced by fluorine, as in manufacture of 3,3,3-trifluoropropene [677-21 ] (14) for use in polyfluorosiHcones. [Pg.268]


See other pages where Iron powder, manufacture is mentioned: [Pg.319]    [Pg.190]    [Pg.485]    [Pg.109]    [Pg.382]    [Pg.671]    [Pg.406]    [Pg.503]    [Pg.201]    [Pg.109]    [Pg.689]    [Pg.710]    [Pg.109]    [Pg.504]    [Pg.428]    [Pg.54]    [Pg.261]    [Pg.817]    [Pg.119]    [Pg.111]    [Pg.188]    [Pg.110]    [Pg.24]    [Pg.545]    [Pg.168]    [Pg.301]    [Pg.87]    [Pg.1959]    [Pg.437]    [Pg.15]    [Pg.55]    [Pg.305]    [Pg.337]   
See also in sourсe #XX -- [ Pg.710 ]

See also in sourсe #XX -- [ Pg.817 ]




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