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Transition metal oxides molybdenum oxide

This process has many similarities to the Phillips process and is based on the use of a supported transition metal oxide in combination with a promoter. Reaction temperatures are of the order of 230-270°C and pressures are 40-80 atm. Molybdenum oxide is a catalyst that figures in the literature and promoters include sodium and calcium as either metals or as hydrides. The reaction is carried out in a hydrocarbon solvent. [Pg.211]

A thin layer deposited between the electrode and the charge transport material can be used to modify the injection process. Some of these arc (relatively poor) conductors and should be viewed as electrode materials in their own right, for example the polymers polyaniline (PAni) [81-83] and polyethylenedioxythiophene (PEDT or PEDOT) [83, 841 heavily doped with anions to be intrinsically conducting. They have work functions of approximately 5.0 cV [75] and therefore are used as anode materials, typically on top of 1TO, which is present to provide lateral conductivity. Thin layers of transition metal oxide on ITO have also been shown [74J to have better injection properties than ITO itself. Again these materials (oxides of ruthenium, molybdenum or vanadium) have high work functions, but because of their low conductivity cannot be used alone as the electrode. [Pg.537]

Solid catalysts for the metathesis reaction are mainly transition metal oxides, carbonyls, or sulfides deposited on high surface area supports (oxides and phosphates). After activation, a wide variety of solid catalysts is effective, for the metathesis of alkenes. Table I (1, 34 38) gives a survey of the more efficient catalysts which have been reported to convert propene into ethene and linear butenes. The most active ones contain rhenium, molybdenum, or tungsten. An outstanding catalyst is rhenium oxide on alumina, which is active under very mild conditions, viz. room temperature and atmospheric pressure, yielding exclusively the primary metathesis products. [Pg.136]

Adam and Lohray122 have used thianthrene 5-oxide (88) as a mechanistic probe in oxidations with transition metal peroxides. They oxidized 88 with various diperoxo complexes of chromium, molybdenum and tungsten and formulated a plausible mechanism on the basis of the products formed, 89 and 90. [Pg.74]

The cations in transition metal oxides often occur in more than one oxidation state. Molybdenum oxide is a good example, as the Mo cation may be in the 6-r, 5-r, and 4+ oxidation states. Oxide surfaces with the cation in the lower oxidation state are usually more reactive than those in the highest oxidation state. Such ions can engage in reactions that involve changes in valence state. [Pg.175]

Other transition-metal oxidants can convert alkenes to epoxides. The most useful procedures involve /-butyl hydroperoxide as the stoichiometric oxidant in combination with vanadium, molybdenum, or titanium compounds. The most reliable substrates for oxidation are allylic alcohols. The hydroxyl group of the alcohol plays both an activating and a stereodirecting role in these reactions. /-Butyl hydroperoxide and a catalytic amount of VO(acac)2 convert allylic alcohols to the corresponding epoxides in good yields.44 The reaction proceeds through a complex in which the allylic alcohol is coordinated to... [Pg.760]

The oxide tetrafluorides and dioxide difluorides of molybdenum and tungsten are the most studied transition-metal oxide fluorides, and their preparation and properties are discussed separately below. [Pg.78]

The group 5-7 supported transition metal oxides (of vanadium, niobium, tantalum, chromium, molybdenum, tungsten, and rhenium) are characterized by terminal oxo bonds (M =0) and bridging oxygen atoms binding the supported oxide to the cation of the support (M -0-MSUpport). The TOF values for ODH of butane or ethane on supported vanadia were found to depend strongly on the specific oxide support, varying by a factor of ca. 50 (titania > ceria > zirconia > niobia > alumina > silica). [Pg.102]

Theory of physical and chemical behavior of transition metal oxides vanadium and molybdenum oxides... [Pg.136]

Oxidation of ammonia to nitrite, N02, and nitrate, N03, is called nitrification the reverse reaction is ammonification. Reduction from nitrite to nitrogen is called denitrification. All these reactions, and more, occur in enzyme systems, many of which include transition metals. A molybdenum enzyme, nitrate reductase, reduces nitrate to nitrite. Further reduction to ammonia seems to proceed by 2-electron steps, through an uncertain intermediate with a -fl oxidation state (possibly hyponitrite, N202 ) and hydroxylamine ... [Pg.612]

Perhaps the most important area of biochemistry in which ESR is used is the study of metalloproteins. Transition metals in certain oxidation and spin states have unpaired electrons, are paramagnetic, and in many cases are amenable to ESR spectroscopy. The most commonly found transition metals in biological systems are iron, copper, molybdenum, cobalt, and manganese. The remainder, including metals such as vanadium and... [Pg.200]

Transition Metal Salts and Oxides on Alumina. Transition metal salts, particularly chlorides and nitrates, are frequently used as starting materials for the preparation of supported transition metal oxides or supported precursors for supported metal catalysts. Also, many catalytic materials, particularly supported molybdenum and tungsten oxide and sulfide catalysts, contain transition metal ions, namely Co, Ni , and Fe " as promoters. Thus, it is interesting to study the spreading and wetting behavior of salts of these transition metals and of their oxides. This is of particular importance for promoted catalyst materials, since in practice the incorporation of the active phase and the promoter should be possible in one step for economic reasons. [Pg.25]

Bulk Mixed Oxide Catalysts. - Raman spectroscopy of bulk transition metal oxides encompasses a vast and well-established area of knowledge. Hie fundamental vibrational modes for many of the transitional metal oxide complexes have already been assigned and tabulated for systems in the solid and solution phases. Perhaps the most well-known and established of the metal oxides are the tungsten and molybdenum oxides because of their excellent Raman signals and applications in hydrotreating and oxidation catalysis. Examples of these two very important metal-oxide systems are presented below for bulk bismuth molybdate catalysts, in this section, and surface (two-dimensional) tungstate species in a later section. [Pg.121]

In this section we describe INS studies of molybdenum trioxide, a precmsor of molybdenum disulfide catalysts ( 7.5), and transition metal oxides which catalyse complete or partial oxidation of hydrocarbons, and copper zinc oxide catalysts, which catalyse methanol synthesis from carbon monoxide and dihydrogen ( 7.3.3). [Pg.330]


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See also in sourсe #XX -- [ Pg.51 , Pg.53 ]




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