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Vanadium and

Chemical reduction. The injection of ammonia reduces NO emissions by the reduction of NO , to nitrogen and water. Although it can be used at higher temperatures without a catalyst, the most commonly used method injects the ammonia into the flue gas upstream of a catalyst bed (typically vanadium and/or tin on a silica support). [Pg.308]

The copolymers of ethylene and propylene (OCVP) are obtained by coordination catalysis using a derivative of vanadium and a derivative of an aluminum alkyl. Molar compositions of ethylene and propylene are usually on the order 45 and 55%. [Pg.356]

In the older form of the periodic table, chromium was placed in Group VI, and there are some similarities to the chemistry of this group (Chapter 10). The outer electron configuration, 3d 4s. indicates the stability of the half-filled d level. 3d 4s being more stable than the expected 3d 4s for the free atom. Like vanadium and titanium, chromium can lose all its outer electrons, giving chromium)VI) however, the latter is strongly oxidising and is... [Pg.376]

Vanadium and its compounds are toxic and should be handled with care. The maximum allowable concentrahon of V2O5 dust in air is about 0.05 (8-hour hme-weighted average -40-hour week). [Pg.72]

Alloys with other useful properties can be obtained by using yttrium as an additive. The metal can be used as a deoxidizer for vanadium and other nonferrous metals. The metal has a low cross section for nuclear capture. 90Y, one of the isotopes of yttrium, exists in equilibrium with its parent 90Sr, a product of nuclear explosions. Yttrium has been considered for use as a nodulizer for producing nodular cast iron, in which the graphite forms compact nodules instead of the usual flakes. Such iron has increased ductility. [Pg.74]

Several forms of magnesium vanadates have been characterized. Some physical properties ate summarized in Table 27 (28—30) (see also Vanadium AND VANADIUM ADLOYS). [Pg.359]

The oxidation of methacrolein to methacrylic acid is most often performed over a phosphomolybdic acid-based catalyst, usually with copper, vanadium, and a heavy alkaU metal added. Arsenic and antimony are other common dopants. Conversions of methacrolein range from 85—95%, with selectivities to methacrylic acid of 85—95%. Although numerous catalyst improvements have been reported since the 1980s (120—123), the highest claimed yield of methacryhc acid (86%) is still that described in a 1981 patent to Air Products (124). [Pg.253]

Under unusual circumstances, toxicity may arise from ingestion of excess amounts of minerals. This is uncommon except in the cases of fluorine, molybdenum, selenium, copper, iron, vanadium, and arsenic. Toxicosis may also result from exposure to industrial compounds containing various chemical forms of some of the minerals. Aspects of toxicity of essential elements have been pubhshed (161). [Pg.388]

Manufacture and Processing. Until World War II, phthaUc acid and, later, phthaUc anhydride, were manufactured primarily by Hquid-phase oxidation of suitable feedstocks. The favored method was BASF s oxidation of naphthalene [91-20-3] by sulfuric acid ia the presence of mercury salts to form the anhydride. This process was patented ia 1896. During World War I, a process to make phthaUc anhydride by the oxidation of naphthalene ia the vapor phase over a vanadium and molybdenum oxide catalyst was developed ia the United States (5). Essentially the same process was developed iadependendy ia Germany, with U.S. patents being granted ia 1930 and 1934 (6,7). [Pg.482]

Impurities that form volatile chlorides leave as gases at the top of the furnace together with the TiCl. By cooling those gases, most impurities, with the exception of vanadium and siUcon chlorides can be separated from the titanium tetrachloride [7550-45-0]. Vanadium chlorides can be reduced to lower oxidation state chlorides that are soHds highly volatile SiCl can be removed from TiCl by fractional distillation. [Pg.9]

A typical Ziegler-Natta catalyst might be made from TiCl or TiCl and Al(C2H )3. Vanadium and cobalt chlorides are also used, as is A1(C2H3)2C1. When these substances are mixed in an inert solvent, a crystalline soHd is obtained. Early catalysts consisted of the finely divided soHd alone, but in modern catalysts, it is often supported on Si02 or MgCl2. [Pg.437]

Catalysts. Commercial sulfuric acid catalysts typically consist of vanadium and potassium salts supported on sUica, usually diatomaceous earth (see Diatomite). Catalyst peUets are available in various formulations, shapes, and sizes depending on the manufacturer and the particular converter pass in which they are to be used. A detailed discussion of oxidation catalysts for sulfuric acid production is available (107). [Pg.187]

Physical methods of fractionation of tar sand bitumen usually indicate high proportions of nonvolatile asphaltenes and resins, even in amounts up to 50% wt/wt (or higher) of the bitumen. In addition, the presence of ash-forming metallic constituents, including such organometaUic compounds as those of vanadium and nickel, is also a distinguishing feature of bitumen. [Pg.351]

To ensure the mtile crystal form, seed crystals are added, otherwise anatase is obtained. The precipitate is thoroughly washed using water and sulfuric acid to remove all traces of discoloring elements, eg, iron, chromium, vanadium, and manganese. The TiO(OH)2 is finally calcined at 1000°C to Ti02 (8). [Pg.97]

Ferrovanadium can also be prepared by the thermite reaction, in which vanadium and iron oxides are co-reduced by aluminum granules in a magnesite-lined steel vessel or in a water-cooled copper cmcible (11) (see Aluminumand aluminum alloys). The reaction is initiated by a barium peroxide—aluminum ignition charge. This method is also used to prepare vanadium—aluminum master alloys for the titanium industry. [Pg.383]

Because no process has been developed for selectively removing impurities in vanadium and vanadium alloys in the metallic state, it is essential that all starting materials, in aggregate, be pure enough to meet final product purity requirements. In addition, the consoHdation method must be one that prevents contamination through reaction with air or with the mold or container material. [Pg.384]

Consolidation. ConsoHdation by the consumable-electrode electric-arc melting technique is ideally suited for vanadium and is used extensively... [Pg.384]


See other pages where Vanadium and is mentioned: [Pg.240]    [Pg.191]    [Pg.128]    [Pg.66]    [Pg.127]    [Pg.265]    [Pg.279]    [Pg.287]    [Pg.398]    [Pg.429]    [Pg.726]    [Pg.755]    [Pg.859]    [Pg.1046]    [Pg.1046]    [Pg.391]    [Pg.502]    [Pg.267]    [Pg.457]    [Pg.477]    [Pg.161]    [Pg.353]    [Pg.564]    [Pg.379]    [Pg.271]    [Pg.381]    [Pg.381]    [Pg.381]    [Pg.382]    [Pg.382]    [Pg.383]    [Pg.383]    [Pg.384]    [Pg.385]   


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1.3- Cyclopentadiene titanium and vanadium complexes

Aluminium and vanadium

Compounds of Vanadium, Niobium and Tantalum

Effect of Vanadium Compounds on Growth and Development

Furan, tetrahydro vanadium, and zirconium complexes

Group 5 (Vanadium, Niobium and Tantalum)

Hydride Compounds of the Titanium and Vanadium Group Elements

Inorganic and Coordination Compounds of Vanadium

Interaction of Vanadium with Proteins and Protein Substrates

Molybdenum and Vanadium Phosphates

Molybdenum, Tungsten, Vanadium and Chromium

Niobium and vanadium

Nutrition and Toxicology of Vanadium

Related Compounds of Vanadium, Niobium, and Tantalum

Saccharinates, of chromium and vanadium

Sodium vanadium and

Structural Vanadium Analogues of Phosphate Esters and Anhydrides

The Aqueous Vanadium(III, IV and V) Systems

The charge density in vanadium and chromium

The sulphides of vanadium, niobium, and tantalum

Titanium, Vanadium, Manganese, and Their Congeners

Tungsten, Vanadium, and Chromium

VANADIUM, NIOBIUM, AND TANTALUM

Vanadium (II), (III), and (IV)

Vanadium Borate and Borophosphate Cluster Anions

Vanadium Compounds on Biological Systems Cellular Growth, Oxidation-Reduction Pathways, and Enzymes

Vanadium Transport and Binding Proteins

Vanadium and nickel

Vanadium and tantalum

Vanadium and the Nitrogen Cycle

Vanadium complex compounds cation, hexaammine, and

Vanadium complexes humic and fulvic acids

Vanadium isotopes and their properties

Vanadium occurrence, extraction and uses

Vanadium, Niobium and Tantalum Carbides

Vanadium, Niobium, Tantalum, and Protactinium

Vanadium, and uranium

Vanadium- and Phosphate-metabolising Enzymes

Vanadium-containing zeotype and ordered mesoporous materials

Vitro Studies of Vanadium Speciation and Redox Chemistry

Water, iridium complex vanadium and chromium complexes

Ziegler-Natta, Phillips, and Vanadium Catalysts

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