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Vanadium water

Figure 1 Potential versus pH diagram for the vanadium-water system at 25 °C. The dashed lines indicate the domains of relative predominance of the dissolved forms of the metal, but the various dissolved forms for each oxidation state are not explicit. The solid lines correspond to saturated solutions with a total vanadium concentration of 0,51 gdm-3. The long dashed lines correspond to oxidation and reduction of water (for E° values of 1.23 and 0.00 V respectively) (adapted from E. Deitombe, N. Zoubov and M. Pourbaix, in Atlas d Equilibres Electrochimiques , ed. M. Pourbaix,... Figure 1 Potential versus pH diagram for the vanadium-water system at 25 °C. The dashed lines indicate the domains of relative predominance of the dissolved forms of the metal, but the various dissolved forms for each oxidation state are not explicit. The solid lines correspond to saturated solutions with a total vanadium concentration of 0,51 gdm-3. The long dashed lines correspond to oxidation and reduction of water (for E° values of 1.23 and 0.00 V respectively) (adapted from E. Deitombe, N. Zoubov and M. Pourbaix, in Atlas d Equilibres Electrochimiques , ed. M. Pourbaix,...
The y is also integral constituent of the alchemical symbol for several varieties of wine (vinum), two of which are shown in Figure 6.1 (left). French and Californian red wines in fact can contain up to 90 ptg of vanadium per litre,[ l i.e. about twice the amount present in the Vanadium Water from the Fuji region (Chapter 1, Figure 1.5). Whether or not drinking red wine has any implications as to the creativity of vanadium chemists remains to be disclosed. [Pg.204]

Vanadium Water quality, water pollution Photometry, catalytic effect... [Pg.295]

Vanadyl Chloride Vanadium Water Displacing Oil Oil Penetrating... [Pg.168]

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]

Vanadium IlI) bromide, VBr3. Dark green or black (V plus Br2) gives green solution in water and green crystalline VBr3,6H20. Forms many complexes. [Pg.416]

Vanadium IV) chloride, VCI4, b.p. 154 C. Reddish brown liquid formed V plus CI2. Decomposes slowly to VCI3 and CU hydrolysed by water. [Pg.417]

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. [Pg.417]

Vanadium pentafiuoride, VF5, m.p. 19-5 C, b.p. 48°C. White solid immediately hydrolysed by water via VOF3 and VO2F. VF5 prepared V plus Fj. Forms hexafluorovanadates(V), MVFe, most easily in BrFj. [Pg.417]

Solids materials that are insoluble in hydrocarbon or water can be entrained in the crude. These are called bottom sediments and comprise fine particles of sand, drilling mud, rock such as feldspar and gypsum, metals in the form of minerals or in their free state such as iron, copper, lead, nickel, and vanadium. The latter can come from pipeline erosion, storage tanks, valves and piping systems, etc. whatever comes in contact with the crude oil. [Pg.327]

C. Fumaric acid from furfural. Place in a 1-litre three-necked flask, fitted with a reflux condenser, a mechanical stirrer and a thermometer, 112 5 g. of sodium chlorate, 250 ml. of water and 0 -5 g. of vanadium pentoxide catalyst (1), Set the stirrer in motion, heat the flask on an asbestos-centred wire gauze to 70-75°, and add 4 ml. of 50 g. (43 ml.) of technical furfural. As soon as the vigorous reaction commences (2) bvi not before, add the remainder of the furfural through a dropping funnel, inserted into the top of the condenser by means of a grooved cork, at such a rate that the vigorous reaction is maintained (25-30 minutes). Then heat the reaction mixture at 70-75° for 5-6 hours (3) and allow to stand overnight at the laboratory temperature. Filter the crystalline fumaric acid with suction, and wash it with a little cold water (4). Recrystallise the crude fumaric acid from about 300 ml. of iif-hydrochloric acid, and dry the crystals (26 g.) at 100°. The m.p. in a sealed capillary tube is 282-284°. A further recrystaUisation raises the m.p. to 286-287°. [Pg.463]

The vanadium pentoxide catalyst Is prepared as follows Suspend 5 g. of pure ammonium vanadate in 50 ml. of water and add slowly 7 5 ml. of pure concentrated hydrochloric acid. Allow the reddish-brown, semi-colloidal precipitate to settle (preferably overnight), decant the supernatant solution, and wash the precipitate several times by decantation. Finally, suspend the precipitate in 76 ml. of water and allow it to stand for 3 days. This treatment renders the precipitate granular and easy to 6lter. Filter the precipitate with suction, wash it several times with cold 5 p>er cent, sodium chloride solution to remove hydrochloric acid. Dry the product at 120° for 12 hours, grind it in a mortar to a fine powder, and heat again at 120° for 12 hours. The yield of catalyst is about 3 - 5 g. [Pg.463]

Pure vanadium is a bright white metal, and is soft and duchle. It has good corrosion resistance to alkalis, sulfuric and hydrochloric acid, and salt water, but the metal oxidizes readily above 660oC. [Pg.72]

Vanadium Dissolve 2.2963 g NH4VO3 in 100 ml of water plus 10 ml of HNO3 dilute to volume. [Pg.1186]

The catalyst used in the production of maleic anhydride from butane is vanadium—phosphoms—oxide (VPO). Several routes may be used to prepare the catalyst (123), but the route favored by industry involves the reaction of vanadium(V) oxide [1314-62-1] and phosphoric acid [7664-38-2] to form vanadyl hydrogen phosphate, VOHPO O.5H2O. This material is then heated to eliminate water from the stmcture and irreversibly form vanadyl pyrophosphate, (V(123,124). Vanadyl pyrophosphate is befleved to be the catalyticaHy active phase required for the conversion of butane to maleic anhydride (125,126). [Pg.454]

The tert-huty hydroperoxide is then mixed with a catalyst solution to react with propylene. Some TBHP decomposes to TBA during this process step. The catalyst is typically an organometaHic that is soluble in the reaction mixture. The metal can be tungsten, vanadium, or molybdenum. Molybdenum complexes with naphthenates or carboxylates provide the best combination of selectivity and reactivity. Catalyst concentrations of 200—500 ppm in a solution of 55% TBHP and 45% TBA are typically used when water content is less than 0.5 wt %. The homogeneous metal catalyst must be removed from solution for disposal or recycle (137,157). Although heterogeneous catalysts can be employed, elution of some of the metal, particularly molybdenum, from the support surface occurs (158). References 159 and 160 discuss possible mechanisms for the catalytic epoxidation of olefins by hydroperoxides. [Pg.138]

Sulfur Polymer Cement. SPC has been proven effective in reducing leach rates of reactive heavy metals to the extent that some wastes can be managed solely as low level waste (LLW). When SPC is combined with mercury and lead oxides (both toxic metals), it interacts chemically to form mercury sulfide, HgS, and lead sulfide, PbS, both of which are insoluble in water. A dried sulfur residue from petroleum refining that contained 600-ppm vanadium (a carcinogen) was chemically modified using dicyclopentadiene and oligomer of cyclopentadiene and used to make SC (58). This material was examined by the California Department of Health Services (Cal EPA) and the leachable level of vanadium had been reduced to 8.3 ppm, well below the soluble threshold limit concentration of 24 ppm (59). [Pg.126]

The Lo-Cat process, Hcensed by US Filter Company, and Dow/Shell s SulFerox process are additional Hquid redox processes. These processes have replaced the vanadium oxidizing agents used in the Stretford process with iron. Organic chelating compounds are used to provide water-soluble organometaHic complexes in the solution. As in the case of Stretford units, the solution is regenerated by contact with air. [Pg.214]

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]

The principal vanadium-bearing ores are generally cmshed, ground, screened, and mixed with a sodium salt, eg, NaCl or Na2C02- This mixture is roasted at ca 850°C and the oxides are converted to water-soluble sodium metavanadate, NaVO. The vanadium is extracted by leaching with water and precipitates at pH 2—3 as sodium hexavanadate, Na V O, a red cake, by the addition of sulfuric acid. This is then fused at 700°C to yield a dense black product which is sold as technical-grade vanadium pentoxide. This product contains a minimum of 86 wt % V20 and a maximum of 6—10 wt % Na20. [Pg.382]

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]

Vanadium(IV) Oxysulfate. Vanadium(IV) oxysulfate pentahydrate (vanadyl sulfate), VOSO4 -5H20) is an ethereal blue sohd and is readily soluble in water. It forms from the reduction of V20 by SO2 in sulfuric acid solution. Vanadium(III) sulfate [13701 -70-7] ) is a powerful... [Pg.391]


See other pages where Vanadium water is mentioned: [Pg.10]    [Pg.253]    [Pg.254]    [Pg.813]    [Pg.10]    [Pg.253]    [Pg.254]    [Pg.813]    [Pg.247]    [Pg.373]    [Pg.417]    [Pg.746]    [Pg.128]    [Pg.540]    [Pg.107]    [Pg.243]    [Pg.391]    [Pg.502]    [Pg.188]    [Pg.298]    [Pg.353]    [Pg.506]    [Pg.73]    [Pg.383]    [Pg.385]    [Pg.385]    [Pg.390]    [Pg.391]    [Pg.392]    [Pg.392]    [Pg.392]    [Pg.393]   
See also in sourсe #XX -- [ Pg.19 , Pg.76 , Pg.130 , Pg.136 ]

See also in sourсe #XX -- [ Pg.32 , Pg.35 , Pg.36 ]




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