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Alloys and hydrogenation

Hydrogen Storage Alloy and Hydrogen Storage Systems, http //www.jmcusa.com/mhl.html, Japan Metal and Chemical Company (USA), Inc, April 2007. [Pg.405]

A. Memezawa, K. Aoki, T. Masumoto, Amorphization of Ti-Zr powders by the collaborated interaction of mechanical alloying and hydrogenation, Sen Metall. Mater. 28 (1993) 361-365. [Pg.186]

Morphology of particles of an initial alloy and hydrogenation products was investigated on electronic focused beam microscope MREM-100. [Pg.322]

Very small quantities of bismuthine are obtained when a bismuth-magnesium alloy, BijMgj, is dissolved in hydrochloric acid. As would be expected, it is extremely unstable, decomposing at room temperature to bismuth and hydrogen. Alkyl and aryl derivatives, for example trimethylbismuthine, Bi(CHj)3, are more stable. [Pg.227]

Finely divided palladium is a good catalyst and is used for hydrogenation and dehydrogenation reactions. It is alloyed and used in jewelry trades. [Pg.112]

Titanium hydride is used as a source for Ti powder, alloys, and coatings as a getter in vacuum systems and electronic tubes as a sealer of metals and as a hydrogen source. [Pg.300]

Nickel sulfide, NiS, can be prepared by the fusion of nickel powder with molten sulfur or by precipitation usiag hydrogen sulfide treatment of a buffered solution of a nickel(II) salt. The behavior of nickel sulfides ia the pure state and ia mixtures with other sulfides is of iaterest ia the recovery of nickel from ores, ia the high temperature sulfide corrosion of nickel alloys, and ia the behavior of nickel-containing catalysts. [Pg.11]

Sihca is reduced to siUcon at 1300—1400°C by hydrogen, carbon, and a variety of metallic elements. Gaseous siUcon monoxide is also formed. At pressures of >40 MPa (400 atm), in the presence of aluminum and aluminum haUdes, siUca can be converted to silane in high yields by reaction with hydrogen (15). SiUcon itself is not hydrogenated under these conditions. The formation of siUcon by reduction of siUca with carbon is important in the technical preparation of the element and its alloys and in the preparation of siUcon carbide in the electric furnace. Reduction with lithium and sodium occurs at 200—250°C, with the formation of metal oxide and siUcate. At 800—900°C, siUca is reduced by calcium, magnesium, and aluminum. Other metals reported to reduce siUca to the element include manganese, iron, niobium, uranium, lanthanum, cerium, and neodymium (16). [Pg.471]

MetaHic potassium and potassium—sodium alloys are made by the reaction of sodium with fused KCl (8,98) or KOH (8,15). Calcium metal and calcium hydride are prepared by the reduction of granular calcium chloride with sodium or sodium and hydrogen, respectively, at temperatures below the fusion point of the resulting salt mixtures (120,121). [Pg.169]

TJItrahigh (99.999 + %) purity tellurium is prepared by zone refining in a hydrogen or inert-gas atmosphere. Single crystals of tellurium, tellurium alloys, and metal teUurides are grown by the Bridgman and Czochralski methods (see Semiconductors). [Pg.386]

Even in good alloys and under favorable conditions, the a value does not lie above about 0.6. In enamelled storage tanks where the current requirement is low, the a value can fall to as low as about 0.1. The cause of the high proportion of selfcorrosion is hydrogen evolution, which occurs as a parallel cathodic reaction according to Eq. (6-5b) or by free corrosion of material separated from the anode on the severely craggy surface [2-4, 19-21]. [Pg.191]

To avoid decarburization and Assuring of the carbon and low-alloy steels, which is cumulative with time and, for all practical purposes irreversible, the limitations of the Nelson Curves should be followed religiously, as a minimum. Suitable low-alloy plate materials include ASTM-A204-A, B, and C and A387-A, B, C, D, and E, and similarly alloyed materials for pipe, tubes, and castings, depending upon stream temperatures and hydrogen partial pressures, as indicated by the Nelson Curves. [Pg.258]

CaNi5, H2, MeOH, H20. The catalyst is a hydrogen storage alloy and is partially consumed by the reaction of Ca with water or methanol. [Pg.533]


See other pages where Alloys and hydrogenation is mentioned: [Pg.191]    [Pg.184]    [Pg.111]    [Pg.379]    [Pg.191]    [Pg.184]    [Pg.111]    [Pg.379]    [Pg.137]    [Pg.131]    [Pg.417]    [Pg.456]    [Pg.321]    [Pg.369]    [Pg.170]    [Pg.14]    [Pg.244]    [Pg.220]    [Pg.347]    [Pg.376]    [Pg.136]    [Pg.104]    [Pg.129]    [Pg.381]    [Pg.432]    [Pg.433]    [Pg.292]    [Pg.420]    [Pg.244]    [Pg.280]    [Pg.48]    [Pg.971]    [Pg.2452]    [Pg.133]    [Pg.258]    [Pg.262]    [Pg.991]    [Pg.190]    [Pg.430]   
See also in sourсe #XX -- [ Pg.110 , Pg.111 , Pg.112 , Pg.113 , Pg.114 , Pg.115 ]




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