Vanadium nitrates

Vanadium Nitrates.—No nitrates of vanadium have been isolated. When hypovanadic oxide is dissolved in nitric acid the blue solution which results probably contains vanadyl nitrate, V0(N03)2, but on evaporation oxidation ensues and hydrated vanadium pentoxide is obtained. Blue solutions of vanadyl nitrate arc more conveniently obtained by precipitating vanadyl chloride with silver nitrate or vanadyl sulphate with barium nitrate. Addition of nitric acid to hexammino-vanadium trichloride yields hexammino-vanadium nitrate,10 [V (NH3)6](N03)3. 

Amino-4-nitropheno1 is produced commercially by the partial reduction of 2,4-dinitrophenol This reduction may be achieved electrolyticaHy using vanadium (159) or chemically with polysulftde, sodium hydrosulftde, or hydrazine and copper (160). Alternatively, 2-acetamidophenol or 2-methylbenzoxazole may be nitrated in sulfuric acid to yield a mixture of 4- and 5-nitro derivatives that are then separated and hydrolyzed with sodium hydroxide (161). 

Failure to consider listed chemical qualifier. Aluminum, vanadium and zinc are qualified as fume or dust." Isopropyl alcohol and saccharin have manufacturing qualifiers. Ammonium nitrate and ammonium sulfate are qualified as solutions. Phosphorus is qualified as yellow or white. Asbestos is qualified as friable. Only chemicals meeting the qualifiers require reporting under section 313 and should be reported on Form R with the appropriate qualifier in parenthesis. 

Discussion. Molybdates [Mo(VI)] are quantitatively reduced in 2M hydrochloric acid solution at 60-80 °C by the silver reductor to Mo(V). The reduced molybdenum solution is sufficiently stable over short periods of time in air to be titrated with standard cerium(IV) sulphate solution using ferroin or /V-phenylanthranilic acid as indicator. Nitric acid must be completely absent the presence of a little phosphoric(V) acid during the reduction of the molybdenum(VI) is not harmful and, indeed, appears to increase the rapidity of the subsequent oxidation with cerium(IV) sulphate. Elements such as iron, copper, and vanadium interfere nitrate interferes, since its reduction is catalysed by the presence of molybdates. 

Determination of vanadium as silver vanadate Discussion. Vanadates are precipitated by excess of silver nitrate solution in the presence of sodium acetate after boiling, the precipitate consists of silver orthovanadate. The following reactions occur with a solution of a metavanadate ... 

Large amounts of chloride, cobalt(II), and chromium(III) do not interfere iron(III), nickel, molybdenum)VI), tungsten(VI), and uranium(VI) are innocuous nitrate, sulphate, and perchlorate ions are harmless. Large quantities of magnesium, cadmium, and aluminium yield precipitates which may co-precipitate manganese and should therefore be absent. Vanadium causes difficulties only... 

Z 1 Niobium 1 Nitrate 1 Osmium 73 a. I Perchlorate Phenols u a o Platinum o 0. 1 5 u 1 Rhodium 1 Rubidium Ruthenium Scandium 1 Selenium Silver I Sodium 1 Strontium 1 Sulphate Sulphides, organic Sulphur dioxide 1 Tantalum 1 Tellurium 1 Thallium Thorium e H 1 Titanium a u ab a 1- I Uranium 1 Vanadium 1 Yttrium 1 Zinc Zirconium... 

Dining outgassing of scrap uranium-aluminium cermet reactor cores, powerful exotherms led to melting of 9 cores. It was found that the incident was initiated by reactions at 350°C between aluminium powder and sodium diuranate, which released enough heat to initiate subsequent exothermic reduction of ammonium uranyl hexafluoride, sodium nitrate, uranium oxide and vanadium trioxide by aluminium, leading to core melting. 

The effect of inorganic additives upon ignition delay in anilinium nitrate-red finning nitric acid systems was examined. The insoluble compounds copper(I) chloride, potassium permanganate, sodium pentacyanonitrosylferrate and vanadium(V) oxide were moderately effective promoters, while the soluble ammonium or sodium metavanadates were very effective, producing vigorous ignition. 

Vanadium oxytri nitrate is an easy to handle reagent that can be used to nitrate a range of substituted aromatic compounds in dichloromethane at room temperature, leading to >99% yields of nitration products (Eq. 2.5).16... 

Vanadium(V) oxytrinitrate [VO(N03)3] has been established as a powerful but moisture-sensitive reagent which nitrates a range of substituted aromatic compounds in good yield in dichloromethane at room temperature. The hydrated triflates Hf(OTf)4 and Zr(OTf)4 are excellent recyclable catalysts for the mononitration of o-nitrotoluene with 1 equiv. of concentrated nitric acid. ... 

Major constituents (greater than 5 mg/L) Minor constituents (O.Ol-lO.Omg/L) Selected trace constituents (less than 0.1 mg/L) Bicarbonate, calcium, carbonic acid, chloride, magnesium, silicon, sodium, sulfate Boron, carbonate, fluoride, iron, nitrate, potassium, strontium Aluminum, arsenic, barium, bromide, cadmium, chromium, cobalt, copper, gold, iodide, lead, Uthium, manganese, molybdenum, nickel, phosphate, radium, selenium, silver, tin, titanium, uranium, vanadium, zinc, zirconium... 

The vendor claims that the following metals have been successfully treated to parts per biUion (ppb) and detection limit levels aluminum, arsenic, cadmium, chromium, cobalt, copper, iron, lead, manganese, mercury, molybdenum, nickel, selenium, silver, tin, uranium, vanadium, and zinc. The system is also able to remove ammonia, nitrates, phosphates, potassium, fluorides, and sodium. Studies have also been performed using Aqua-Fix to remove radionuchdes such as uranium from waste streams. 

The spray method was used to produce alumina pigments doped with Cr, Mn, and Co. In these experiments, Al(.vec-OBu)3 was mixed with solutions of the corresponding metal nitrates in. veobutoxide, the resulting liquids were nebulized, and then the droplets were hydrolyzed (76). The major purpose of these studies was to obtain inorganic pigments and to evaluate their color properties by altering the amount of dopants in the aluminum oxide matrix. For the same reason, the vanadium... 

The purification of the alkali hydroxides.—Numerous impurities have been reported in commercial sodium and potassium hydroxides. Several have commented on the presence of peroxide, particularly in caustic potash.19 Various salts—carbonate, sulphate, nitrate, nitrite, chloride, and phosphate—as well as alumina, silica, organic matters, and metal oxides—e.g. arsenic, vanadium, iron, etc., have been reported. More or less of the other alkalies may also be present. 

Preparation of Anhydrous Dioxovanadium Nitrate (VO2NO3). Prepare 7-10 ml of liquid nitrogen(IV) oxide (see p. 141). Mix the nitrogen(IV) oxide with 5-7 cm of dry acetonitrile in a test tube (see Fig. 92a). Add 0.3-0.5 g of metallic vanadium preliminarily crushed in a porcelain mortar to this mixture. Close the test tube with a stopper provided with a calcium chloride tube containing phosphoric anhydride. 

In earlier studies mercury has been plated onto electrodes to be used in voltammetric and spectrochemical analysis.2 DeAngelis (1976) developed thin film mercury electrodes by plating a solution of mercuric nitrate onto a variety of different electrodes in order to detect the presence of trace metals in small volumes. The results demonstrated that mercury plating occurred with tungsten, vanadium, chromium, and iron and there was little amalgamation. 

Nitrates and carbonates of vanadium, niobium, and tantalum have not been prepared. Niobium and tantalum salts of other weak acids, e.g. boric add, hydrocyanic add, phosphoric acid, are also unknown, and in the case of vanadium are not well defined. 

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