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Alkalis molybdenum

Alkalis Molybdenum is moderately resistant to aerated solutions of ammonium hydroxide and is inert when oxygen is excluded. It has only fair resistance in aerated 1 % sodium hydroxide at 35°C and 60°C but its resistance is better in a 10% solution at both these temperatures. It is severely corroded in sodium hypochlorite solutions (pH 11 or higher) at 35°C (Table 5.4). [Pg.845]

The base lubricant is usually a petroleum oil while the thickener usually consists of a soap or soap mixture. In addition they may contain small amounts of free alkali, free fatty acid, glycerine, anti-oxidant, extreme-pressure agent, graphite or molybdenum disulphide. [Pg.242]

Molybdenum compounds Hydrodesulphurization and hydrotreating of petroleum Oxidation of methanol to formaldehdye Epoxidation of olefins Decomposition of alkali metal nitrides Irritation of eyes and respiratory tract Pneumoconiosis... [Pg.121]

Boron enflames in contact with IF3 so do P, As and Sb. Molybdenum and W enflame when heated and the alkali metals react violently. KH and CaC2 become incandescent in hot IF3. However, reaction is more sedate with many other metals and non-metals, and compounds such as CaCOs and Ca3(P04)2 appear not to react with the liquid. [Pg.835]

The trioxides of molybdenum and tungsten differ from Cr03 in that, though they are acidic and dissolve in aqueous alkali to give salts of... [Pg.1007]

Cellulose produds There is little scope for the use of austenitic steels in the alkali processes for the digestion of wood pulp, but both molybdenum-free and molybdenum-bearing steels are extensively used for sulphite pulp digestion, choice depending on concentration, temperature and working experience. [Pg.559]

Molybdates yield sparingly soluble orange-yellow molybdyl oxinate with oxine solution the pH of the solution should be between the limits 3.3-7.6. The complex differs from other oxinates in being insoluble in organic solvents and in many concentrated inorganic acids. The freshly precipitated compound dissolves only in concentrated sulphuric acid and in hot solutions of caustic alkalis. This determination is of particular interest, as it allows a complete separation of molybdenum from rhenium. [Pg.461]

K. Chen, S. Xie, A.T. Bell, and E. Iglesia, Alkali effects of molybdenum oxide catalysts for the oxidative dehydrogenation of propane, J. Catal. 195, 244-252 (2000). [Pg.331]

Both of the soils are enriched in various elements, like zirconium, titanium, beryllium, niobium, and strontium, due to their enlarged content in the alkali basalts and phonolites of the East-African Rift. We can see that soils of Tanzanian Dry Savanna ecosystems contain niobium 11 times, beryllium and molybdenum 6 times, and titanium and zirconium 4 times as high as compared to the respective crust concentrations (darks) of these metals. In the Ugandan soils, the chromium content is 7 times higher... [Pg.184]

Supported Rhodium Catalysts Alkali Promoters on Metal Surfaces Cobalt-Molybdenum Sulfide Hydrodesulfurization Catalysts Chromium Oxide Polymerization Catalysts... [Pg.246]

There are a few features relative to POMs that are necessary for obtaining the best performance. In all cases. Vanadium is present in the structure of the P/Mo Keggin anion, while the cations include different components, that is, protons, divalent transition metal ions (preferably either Fe " " or Cu " "), and alkali metal ions (preferably Cs" "). The role of Cu ions is to catalyze the reduction of molybdenum, thus increasing the activity of the catalyst it also affects the surface acidity. [Pg.272]

Molybdenum oxidizes at high temperatures but not at room temperatures. It is insoluble in acids and hydroxides at room temperatures. At room temperatures, all three metals (chromium, molybdenum, and tungsten) resist atmospheric corrosion, which is one reason chromium is used to plate other metals. They also resist attacks from acids and strong alkalis, with the exception of chromium, which, unless in very pure form, will dissolve in hydrochloric acid (HCl). [Pg.128]

Uranium reacts with most nonmetallic elements to form a variety of compounds, all of which are radioactive. It reacts with hot water and dissolves in acids, but not in alkalis (bases). Uranium is unique in that it can form solid solutions with other metals, such as molybdenum, titanium, zirconium, and niobium. [Pg.313]

Molybdenum In its pure form, without additions, it is the most efficient catalyst of all the easily obtainable and reducible substances, and it is less easily poisoned than iron. It catalyzes in another way than iron, insofar as it forms analytically easily detectable amounts of metal nitrides (about 9% nitrogen content) during its catalytic action, whereas iron does not form, under synthesis conditions, analytically detectable quantities of a nitride. In this respect, molybdenum resembles tungsten, manganese and uranium which all form nitrides during their operation, as ammonia catalysts. Molybdenum is clearly promoted by nickel, cobalt and iron, but not by oxides such as alumina. Alkali metals can act favorably on molybdenum, but oxides of the alkali metals are harmful. Efficiency, as pure molybdenum, 1.5%, promoted up to 4% ammonia. [Pg.95]

The anhydrous acid consists of white hexagonal crystals density 3.112 g/cm converts to molybdenum trioxide, M0O3 at 70°C slightly soluble in water soluble in alkalies and sulfuric acid. [Pg.585]

Unlike the trioxide, molybdenum dioxide is stable towards nonoxidizing acids, alkalies or fused salts. [Pg.592]

Molybdenum(VI) oxide is the most stable oxide of molybdenum. It reacts with alkali solutions, forming molybdates ... [Pg.594]

Molybdenum(VI) oxide combines with several metal oxides forming their orthomolyhdates. Such products are obtained as hydrated salts upon neutralization of slurries of M0O3 and the metal oxides with alkalies ... [Pg.594]


See other pages where Alkalis molybdenum is mentioned: [Pg.3420]    [Pg.3442]    [Pg.3419]    [Pg.3441]    [Pg.760]    [Pg.120]    [Pg.3420]    [Pg.3442]    [Pg.3419]    [Pg.3441]    [Pg.760]    [Pg.120]    [Pg.107]    [Pg.535]    [Pg.1010]    [Pg.1016]    [Pg.461]    [Pg.696]    [Pg.441]    [Pg.35]    [Pg.65]    [Pg.207]    [Pg.782]    [Pg.609]    [Pg.667]    [Pg.86]    [Pg.48]    [Pg.123]    [Pg.494]    [Pg.218]    [Pg.159]    [Pg.341]    [Pg.262]   
See also in sourсe #XX -- [ Pg.5 , Pg.17 ]

See also in sourсe #XX -- [ Pg.5 , Pg.17 ]




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