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Vanadium niobium

R. J. H. Clark and D. Brown, The Chemisty of Vanadium, Niobium and Tantalum, Pergamon Press, Ehnsford, N. Y., 1975. [Pg.30]

Borides are inert toward nonoxidizing acids however, a few, such as Be2B and MgB2, react with aqueous acids to form boron hydrides. Most borides dissolve in oxidizing acids such as nitric or hot sulfuric acid and they ate also readily attacked by hot alkaline salt melts or fused alkaU peroxides, forming the mote stable borates. In dry air, where a protective oxide film can be preserved, borides ate relatively resistant to oxidation. For example, the borides of vanadium, niobium, tantalum, molybdenum, and tungsten do not oxidize appreciably in air up to temperatures of 1000—1200°C. Zirconium and titanium borides ate fairly resistant up to 1400°C. Engineering and other properties of refractory metal borides have been summarized (1). [Pg.218]

Table 22.2 Oxidation states and stereochemistries of compounds of vanadium, niobium and tantalum... Table 22.2 Oxidation states and stereochemistries of compounds of vanadium, niobium and tantalum...
The known halides of vanadium, niobium and tantalum, are listed in Table 22.6. These are illustrative of the trends within this group which have already been alluded to. Vanadium(V) is only represented at present by the fluoride, and even vanadium(IV) does not form the iodide, though all the halides of vanadium(III) and vanadium(II) are known. Niobium and tantalum, on the other hand, form all the halides in the high oxidation state, and are in fact unique (apart only from protactinium) in forming pentaiodides. However in the -t-4 state, tantalum fails to form a fluoride and neither metal produces a trifluoride. In still lower oxidation states, niobium and tantalum give a number of (frequently nonstoichiometric) cluster compounds which can be considered to involve fragments of the metal lattice. [Pg.988]

The corrosion behaviour of amorphous alloys has received particular attention since the extraordinarily high corrosion resistance of amorphous iron-chromium-metalloid alloys was reported. The majority of amorphous ferrous alloys contain large amounts of metalloids. The corrosion rate of amorphous iron-metalloid alloys decreases with the addition of most second metallic elements such as titanium, zirconium, vanadium, niobium, tantalum, chromium, molybdenum, tungsten, cobalt, nickel, copper, ruthenium, rhodium, palladium, iridium and platinum . The addition of chromium is particularly effective. For instance amorphous Fe-8Cr-13P-7C alloy passivates spontaneously even in 2 N HCl at ambient temperature ". (The number denoting the concentration of an alloy element in the amorphous alloy formulae is the atomic percent unless otherwise stated.)... [Pg.633]

Hydrogen reduction has a major advantage in that the reaction generally takes place at lower temperature than the equivalent decomposition reaction. It is used extensively in the deposition of transition metals from their halides, particularly the metals of Groups Va, (vanadium, niobium, and tantalum) and Via (chromium, molybdenum, and tungsten). The halide reduction of Group IVa metals (titanium, zirconium, and hafnium) is more difficult because their halides are more stable. [Pg.70]

DAMPS) combined with oxysalts of vanadium, niobium, tantalum or titanium, zirconium, hafnium ... [Pg.102]


See other pages where Vanadium niobium is mentioned: [Pg.110]    [Pg.125]    [Pg.298]    [Pg.98]    [Pg.41]    [Pg.386]    [Pg.976]    [Pg.978]    [Pg.980]    [Pg.981]    [Pg.982]    [Pg.984]    [Pg.986]    [Pg.988]    [Pg.988]    [Pg.989]    [Pg.990]    [Pg.992]    [Pg.993]    [Pg.994]    [Pg.994]    [Pg.996]    [Pg.998]    [Pg.1000]    [Pg.1019]    [Pg.28]    [Pg.394]    [Pg.441]    [Pg.211]    [Pg.218]    [Pg.241]    [Pg.33]    [Pg.365]    [Pg.387]    [Pg.444]    [Pg.455]    [Pg.124]    [Pg.166]    [Pg.20]   
See also in sourсe #XX -- [ Pg.118 ]




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Vanadium, Niobium, Tantalum

Vanadium, Niobium, Tantalum, and Protactinium

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