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Metallic nickel

Ma.nufa.cture. The preferred method for making nickel sulfate is adding nickel powder to hot dilute sulfuric acid. Adding sulfuric acid to nickel powder in hot water enhances the formation of H2S. Hydrogen sulfide always forms as a by-product upon reaction of metallic nickel and sulfuric acid. The hberated hydrogen is absorbed by the metal and then reduces the sulfate anion to H2S. [Pg.10]

Ma.nufa.cture. Nickel carbonyl can be prepared by the direct combination of carbon monoxide and metallic nickel (77). The presence of sulfur, the surface area, and the surface activity of the nickel affect the formation of nickel carbonyl (78). The thermodynamics of formation and reaction are documented (79). Two commercial processes are used for large-scale production (80). An atmospheric method, whereby carbon monoxide is passed over nickel sulfide and freshly reduced nickel metal, is used in the United Kingdom to produce pure nickel carbonyl (81). The second method, used in Canada, involves high pressure CO in the formation of iron and nickel carbonyls the two are separated by distillation (81). Very high pressure CO is required for the formation of cobalt carbonyl and a method has been described where the mixed carbonyls are scmbbed with ammonia or an amine and the cobalt is extracted as the ammine carbonyl (82). A discontinued commercial process in the United States involved the reaction of carbon monoxide with nickel sulfate solution. [Pg.12]

Metallic cobalt, metallic nickel and an alloy powder containing 66-67% nickel, 13-16% chromium and 7% iron... [Pg.101]

The phenol is reduced with hydrogen in presence of finely divided metallic nickel which acts as a catalyst. The apparatus is shown in Fig. 79. [Pg.181]

An alloy of nickel was known in China over 2000 years ago, and Saxon miners were familiar with the reddish-coloured ore, NiAs, which superficially resembles CU2O. These miners attributed their inability to extract copper from this source to the work of the devil and named the ore Kupfemickel (Old Nick s copper). In 1751 A. F. Cronstedt isolated an impure metal from some Swedish ores and, identifying it with the metallic component of Kupfemickel, named the new metal nickel . In 1804 J. B. Richter produced a much purer sample and so was able to determine its physical properties more accurately. [Pg.1144]

Dimethyl-l,2,2,3-tetramethyl-A -1,2,5-azasilaboroline with [Fe2(CO)9] gives sandwich 62 and sandwich 63 (82AGE207, 82CB738) with Cp)Co(C2H4)2]. With [Ni(CDT)] or in a vapor phase with metallic nickel, sandwich 64 (M =Ni) is formed. The vapor-phase synthesis with iron gives 64 (M = Fe). In all these sandwiches, 62-64, the j " -coordination of the heterocyclic ligand is realized. [Pg.24]

Unfortunately, investigations with ionic liquids containing high amounts of AlEtCl2 showed several limitations, including the reductive effect of the alkylaluminium affecting the temperature stability of the nickel catalyst. At very high alkylaluminium concentrations, precipitation of black metallic nickel was observed even at room temperature. [Pg.246]

Increase in the concentration of metals (nickel, vanadium, etc.) on the catalyst... [Pg.183]

In addition to nickel alloys, nickel also forms an important alloying element in stainless steels and in cast irons, in both of which it confers additional corrosion resistance and improved mechanical and engineering properties, and in Fe-Ni alloys for obtaining controlled physical and magnetic properties (see Chapter 3). With non-ferrous metals nickel also forms important types of alloys, especially with copper, i.e. cupro-nickels and nickel silvers these are dealt with in Section 4.2. [Pg.760]

As with alloys of other metals, nickel alloys may suffer stress-corrosion cracking in certain corrosive environments, although the number of alloy environment combinations in which nickel alloys have been reported to undergo cracking is relatively small. In addition, intergranular attack due to grain boundary precipitates may be intensified by tensile stress in the metal in certain environments and develop into cracking. Table 4.28 lists the major circumstances in which stress corrosion or stress-assisted corrosion of nickel and its alloys have been recorded in service and also shows the preventive and remedial measures that have been adopted, usually with success, in each case. [Pg.794]

Table 12-11 predicts the cell will operate so as to dissolve metallic zinc and deposit metallic nickel, and its voltage will be +0.51 volt This is exactly what occurs in such a cell. Predicting is fun— let s try it again Another cell we studied is based on reaction (52) ... [Pg.212]

X-ray analysis of the spent catalyst (Table XI) revealed metallic nickel and nickel carbide, Ni3C, in the catalyst near the gas inlet and only metallic nickel near the gas outlet. [Pg.116]

In addition to actual synthesis tests, fresh and used catalysts were investigated extensively in order to determine the effect of steam on catalyst activity and catalyst stability. This was done by measurement of surface areas. Whereas the Brunauer-Emmett-Teller (BET) area (4) is a measure of the total surface area, the volume of chemisorbed hydrogen is a measure only of the exposed metallic nickel area and therefore should be a truer measure of the catalytically active area. The H2 chemisorption measurement data are summarized in Table III. For fresh reduced catalyst, activity was equivalent to 11.2 ml/g. When this reduced catalyst was treated with a mixture of hydrogen and steam, it lost 27% of its activity. This activity loss is definitely caused by steam since a... [Pg.130]

The last vertical column of the eighth group of the Periodic Table of the Elements comprises the three metals nickel, palladium, and platinum, which are the catalysts most often used in various reactions of hydrogen, e.g. hydrogenation, hydrogenolysis, and hydroisomerization. The considerations which are of particular relevance to the catalytic activity of these metals are their surface interactions with hydrogen, the various states of its adatoms, and admolecules, eventually further influenced by the coadsorbed other reactant species. [Pg.245]

This is the Mond reaction, first developed by Ludwig Mond in 1890. It is still used forthe production and purification of metallic nickel. A similar reaction is used for the production of Fe(CO)5 but higher temperature is required. [Pg.159]

Bottom plate (metal Nickel (or copper) block) material Nickel tubing 500 pm 100 mm internal diameter length... [Pg.587]

Separation of two metals from a leach solution - as examples, mention may be made of solutions containing cobalt and copper, and nickel and copper. The former solution is treated by metallic cobalt to precipitate copper, and the latter by metallic nickel to precipitate copper. In both cases, the metal added to cement the copper is recovered afterwards. [Pg.544]

Plant resins, poison ivy, poison oak, poison sumac Metals (nickel or gold in jewelry)... [Pg.967]

The base metal nickel now begins to plate out on an appropriate surface, such as a less noble metal. [Pg.233]


See other pages where Metallic nickel is mentioned: [Pg.510]    [Pg.132]    [Pg.10]    [Pg.10]    [Pg.14]    [Pg.41]    [Pg.46]    [Pg.544]    [Pg.547]    [Pg.210]    [Pg.288]    [Pg.307]    [Pg.34]    [Pg.318]    [Pg.319]    [Pg.516]    [Pg.1061]    [Pg.535]    [Pg.46]    [Pg.46]    [Pg.81]    [Pg.209]    [Pg.722]    [Pg.535]    [Pg.164]    [Pg.766]    [Pg.551]    [Pg.247]    [Pg.252]    [Pg.299]    [Pg.453]   
See also in sourсe #XX -- [ Pg.345 ]

See also in sourсe #XX -- [ Pg.345 ]

See also in sourсe #XX -- [ Pg.158 ]




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Alloying metals nickel

Alumina-tungsten-nickel catalyst other metals

Batteries applications nickel-metal hydride

Batteries nickel-metal

Batteries nickel-metal hybrid

Batteries nickel-metal hydride battery

Batteries nickel-metal-hydride rechargeable

Batteries, storage nickel-metal hydride

Capacity nickel metal hydride batteries

Cathode nickel metal particle

Cell voltage nickel metal hydride

Chalcogenides, transition metal nickel

Characteristics nickel metal hydroxide

Charging sealed nickel-metal hydride batteries

Containing Metal-Carbon cr-Bonds of the Groups Iron, Cobalt, and Nickel

Electric vehicle batteries nickel metal hydride

Energy nickel-metal hydride

Energy storage materials nickel metal hydride batteries

Gold-nickel-copper metallization

Group 10 metals, dithiocarbamate nickel

Heavy metal removal nickel

Hydrogen nickel alloy weld metal

Iron family metals nickel

Linear metal chain compounds nickel

Metal amorphous nickel

Metal carbonyls Nickel carbonyl

Metal carbonyls nickel tetracarbonyl

Metal carboxylates nickel complex compounds

Metal catalysts Raney nickel

Metal catalysts nickel-alumina

Metal copper-nickel alloys

Metal dusting iron-nickel-based

Metal dusting nickel-based

Metal electrodes nickel

Metal hydride-nickel batterie

Metal hydride-nickel oxide cells

Metal nickel

Metal nickel

Metal nickel compound

Metal salts Nickel

Metal salts Nickel hydroxide

Metal salts Nickel sulfide

Metal salts Nickel-organic complexes

Metal supported nickel catalysts from

Metal tartaric acid-modified nickel

Metal toxicity nickel

Metal, metals nickel

Metal-Carbon r-Bonds of the Groups Iron, Cobalt, and Nickel

Metal-alkyne complexes nickel

Metal-arene complexes nickel

Metallic coatings electroless nickel plating

Metallic nickel films

Metallic nickel, from hydrogenation

Metals mercury nickel silver zinc

Miscellaneous metals including sodium, lithium, ammonium, potassium, magnesium, calcium, lead, copper, cadmium, cobalt, nickel, iron, zinc and 14 lanthanides

Mixed metal oxides nickel compounds

Nickel Group Metals

Nickel Metal Hydride (Ni-MH) accumulator

Nickel Transition Metal Catalysis

Nickel alloy weld metal

Nickel base metal recovery

Nickel complexes metal to semiconductor transition

Nickel complexes metal-sulfur ligand structures

Nickel complexes, metal exchange reactions

Nickel complexes, ring metalation

Nickel compounds transition metal electronic structure

Nickel group metals, complexes with

Nickel ions with metal

Nickel metal carbonyl clusters

Nickel metal dusting

Nickel metal hydride batteries

Nickel metal hydride battery/cell

Nickel metal hydride electrochemical cell

Nickel metal hydride electrode

Nickel metal hydride storage process

Nickel metal hydroxide

Nickel metal hydroxide secondary

Nickel metal, reactions

Nickel mixed-metal clusters

Nickel nonporphyrin metal compounds

Nickel oxide-supported metal catalysts

Nickel passive metal

Nickel porphyrins, metalation

Nickel porphyrins, metalation reactions

Nickel valve metals

Nickel-based alloys metal dusting

Nickel-metal hydride

Nickel-metal hydride batteries, sealed

Nickel-metal hydride batteries, sealed portable)

Nickel-metal hydride cells

Nickel-metal-hydride rechargeable

Of nickel metal

Organometallic complexes, transition metal nickel

Overall nickel metal hydride batteries

Phosphine-metal complexes nickel

Preparation of Metallic Nickel Powders and Their Reaction with 4-Nitrobenzyl Chloride

Preparation of metallic nickel

Propulsion and Industrial Nickel-Metal Hydride Batteries

Reactivity studies, transition metal nickel

Sealed nickel-metal hydride

The Nickel-Metal Hydride Battery (NiMH)

Thin oxide film formation, metal nickel

Transition metal catalysis nickel complexes

Transition metal catalysts with nickel

Transition metal complexes Nickel

Transition metals nickel

What are the electrode materials in nickel-metal-hydride batteries

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