Vanadium oxide, preparation

The photoluminescence of the anchored vanadium oxide prepared by the photo-CVD method was quenched in both its intensity and its lifetime by the addition of trans-2-C4H8, suggesting that the molecules interact with... 

Supported vanadium oxide prepared by impregnation of y-alumina with ammonium vanadate solution, followed by ignition and reduction at 850 in hydrogen, gives the peculiar susceptibility isotherms shown in... 

Vanadium oxide trichloride, VOCI3, vanadyl chloride. Readily prepared yellow liquid, b.p. 127 C, formed CK plus heated V2OS plus C. Readily hydrolysed by water. 

Patents claiming specific catalysts and processes for thek use in each of the two reactions have been assigned to Japan Catalytic (45,47—49), Sohio (50), Toyo Soda (51), Rohm and Haas (52), Sumitomo (53), BASF (54), Mitsubishi Petrochemical (56,57), Celanese (55), and others. The catalysts used for these reactions remain based on bismuth molybdate for the first stage and molybdenum vanadium oxides for the second stage, but improvements in minor component composition and catalyst preparation have resulted in yields that can reach the 85—90% range and lifetimes of several years under optimum conditions. Since plants operate under more productive conditions than those optimum for yield and life, the economically most attractive yields and productive lifetimes maybe somewhat lower. 

Maleic anhydride and the two diacid isomers were first prepared in the 1830s (1) but commercial manufacture did not begin until a century later. In 1933 the National Aniline and Chemical Co., Inc., installed a process for maleic anhydride based on benzene oxidation using a vanadium oxide catalyst (2). Maleic acid was available commercially ia 1928 and fumaric acid production began in 1932 by acid-catalyzed isomerization of maleic acid. 

Vanadium metal can be prepared either by the reduction of vanadium chloride with hydrogen or magnesium or by the reduction of vanadium oxide with calcium, aluminum, or carbon. The oldest and most commonly used method for producing vanadium metal on a commercial scale is the reduction of V20 with calcium. Recently, a two-step process involving the alurninotherniic reduction of vanadium oxide combined with electron-beam melting has been developed. This method makes possible the production of a purer grade of vanadium metal, ie, of the quaUty required for nuclear reactors (qv). 

Tin vanadium yeUows are prepared by introducing small amounts of vanadium oxide into the cassiterite stmcture of Sn02 (28). Tin vanadium... 

The general procedure for the preparation of vanadium borates consists in heating a concentrated H2O solution of boric acid and vanadium oxide in an autoclave at 170 °C for several days [143]. Two different vanadium borate clusters 105 and 106 are obtained, one with two polyborate chains coordinated to a contorted vanadium oxide ring (105) and another one with a macrocyclic Bi8036(0H)6 ring (106). The latter ring is composed of six B306(0H) units and has a chair-like conformation (Fig. 27) [143]. 

The introduction of microwave pr ents an excellent new option for the synthesis of VOPc from vanadium oxide, dicyanobenzene, and ethylene glycol. In the present study, the effectiveness of synthesizing crude VOPc liom vanadium oxide and dicyanobenzene rmder the two synthetic methods was investigate by comparing reaction temperatures. Also, the preparation of fine crystal VOPc was investigated from the crude VOPc synthesized at... 

The surface phase diagram of vanadium oxides on Rh(l 11) has been investigated in a series of papers of our group [4, 18, 19, 90, 101-103]. It is characterized by pronounced polymorphism and many different oxide structures have been detected as a function of coverage and growth temperature. The vanadium oxide structures for coverages up to the completion of the first monolayer formed on Rh(l 11) under the different preparation conditions may be subdivided into highly oxidized phases... 

XRD patterns of the prepared samples V-Mo-Zeolite are similar to that of zeolites which suggests that the metal species (i.e. oxide, cations,...) are well dispersed through the zeolites structure and the absence of bulk phases in the XRD patterns implies that for these samples the molybdenum and vanadium oxides are present in either a nanocrystalline state or as a small crystallites which measured less than 4 nm in diameter. Furthermore, XRD and FTIR (1500-400 cm 1) showed no significant damage of the zeolite host structure after exchange and thermal treatment except for the sample V2MoMor. 

Chen, X.-W. Zhu, Z. Haevecker, M. Su, D.S. Schlogl, R., Carbon nanotube-induced preparation of vanadium oxide nanorods Application as a catalyst for the partial oxidation of n-butane. Materials Res. Bull. 2007,42 354-361. 

Murphy et al. made an extensive study of a number of vanadium oxides and discovered the excellent electrochemical behavior of the partially reduced vanadium oxide, VeOis, which reacts with up to 1 LiA/. They also recognized that the method of preparation, which determines the V 0 ratio, critically controls the capacity for reaction with lithium. The structure consists of alternating double and single sheets of vanadium oxide sheets made up of distorted VOe octahedra. A variety of sites are available for lithium intercalation, which if filled sequentially would lead to the various steps seen in the discharge curve. The lattice first expands along the c-axis and then along the b-axis. Thomas et ai 87 91 an in-depth study of the complex... 

Another vanadium oxide that has received much attention is LiVaOs, which has a layer structure composed of octahedral and trigonal bipyramidal ribbons that can be swelled just like other layered compounds and can intercalate lithium. Here again, the method of preparation is important to its electrochemical characteristics. West et al. made a systematic study of the impact of synthesis technique on capacity and cycling and showed that amorphous material increased the capacity above 2 V from 3—4 lithium per mole of LiVsOs at low current drains, 6—200 fiAlcm. ... 

Ti02 nanotubes were used to support M0O3 observing a spontaneous dispersion of molybdenum-oxide on the surface of nanotubes, which was different from that observed on titania particles.Supporting tungsten oxides a preferential orientation of the (002) planes was observed. Vanadium-oxide in the form of nanorods could be prepared using the titania nanotube as structure-directing template under hydrothermal... 

Niobium Products Co., 50 m /g). Many different synthesis methods have been used to prepare supported metal oxide catalysts. In the case of supported vanadium oxide catalysts, the catalysts were prepared by vapor phase grafting with VOCI3, nonaqueous impregnation (vanadium alkoxides), aqueous impregnation (vanadium oxalate), as well as spontaneous dispersion with crystalline V2O5 [4]. No drastic reduction of surface area of the catalysts was observed. 

The vanadium oxide species is formed on the surface of the oxide support during the preparation of supported vanadium oxide catalysts. This is evident by the consumption of surface hydroxyls (OH) [5] and the structural transformation of the supported metal oxide phase that takes place during hydration-dehydration studies and chemisorption of reactant gas molecules [6]. Recently, a number of studies have shown that the structure of the surface vanadium oxide species depends on the specific conditions that they are observed under. For example, under ambient conditions the surface of the oxide supports possesses a thin layer of moisture which provides an aqueous environment of a certain pH at point of zero charge (pH at pzc) for the surface vanadium oxide species and controls the structure of the vanadium oxide phase [7]. Under reaction conditions (300-500 C), moisture desorbs from the surface of the oxide support and the vanadium oxide species is forced to directly interact with the oxide support which results in a different structure [8]. These structural... 

The surface structure and reactivity of vanadium oxide monolayer catalysts supported on tin oxide were investigated by various physico-chemical characterization techniques. In this study a series of tin oxide supported vanadium oxide catalysts with various vanadia loadings ranging from 0.5 to 6. wt.% have been prepared and were characterized by means of X-ray diffraction, oxygen chemisorption at -78°C, solid state and nuclear magnetic resonance... 

Figure 4. X-Ray diffraction patterns for phosphorous-vanadium oxide catalysts prepared by aerosol technique at 600 C, 8 seconds residence time, and 0.8 M V in feed a. Catalyst analyzed by XRD immediately after synthesis, b. catalyst calcined at 450°C in nitrogen for 3 hrs immediately after synthesis, c. Catalyst allowed to stand for 14 days in an air tight container at ambient temperature without calcining.

Thermal decomposition—Thermal decomposition methods may be used to prepare metal oxide fumes. An aerosol of a precursor to the metal oxide (i.e., a substance that is readily decomposed, thermally, to yield the oxide) is first generated and then is heated by passing it through a heated tube to decompose it to the oxide. Metal formates, oxalates, and the like, which readily yield the oxides and do not produce objectionable side products, are commonly used precursors. In this program, fumes of iron oxide, vanadium oxide, and copper oxide were generated using this method. 

The influence of different preparation methods upon the structure and reactivity of supported vanadia catalysts has recently been investigated by several laboratories.55 58 These studies concluded that the same surface vanadia species forms on a specific oxide support independent of the preparation method, even when starting with V205 crystals. The reason for this phenomenon is that vanadium oxide spontaneously disperses on oxide supports to form surface vanadia species, which is schematically depicted in Figure 7. 

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