Nickel bromate

Nickel Bromate,2 Ni(Br03)2.6H20, may be prepared by double decomposition of barium bromate and nickel sulphate solutions. It crystallises in unstable octahedra which are green in colour. From its solution in aqueous ammonia, alcohol precipitates the diammoniate, Ni(Br03)2.2NH3. 

Hypobromites, the salts of hypobromous acid, do not keep well because they gradually disproportionate to bromide and bromate. Solutions are best prepared as needed from bromine and alkafl with cooling. Because disproportionation is catalyzed by cobalt, nickel, and copper (70), these impurities should be avoided. SoHd alkaline earth hypobromites, or more properly, bromide hypobromites such as calcium bromide hypobromite [67530-61 CaBr(OBr), have been known for many years, but the pure crystalline hydrates sodium hypobromite pentahydrate [13824-96-9] NaOBr 5H20, and potassium hypobromite tribydrate [13824-97-0], KOBr 3H20, were not described until 1952 (71). Hypobromites are strong bleaching agents, similar to hypochlorites. 

The cobalt complex is usually formed in a hot acetate-acetic acid medium. After the formation of the cobalt colour, hydrochloric acid or nitric acid is added to decompose the complexes of most of the other heavy metals present. Iron, copper, cerium(IV), chromium(III and VI), nickel, vanadyl vanadium, and copper interfere when present in appreciable quantities. Excess of the reagent minimises the interference of iron(II) iron(III) can be removed by diethyl ether extraction from a hydrochloric acid solution. Most of the interferences can be eliminated by treatment with potassium bromate, followed by the addition of an alkali fluoride. Cobalt may also be isolated by dithizone extraction from a basic medium after copper has been removed (if necessary) from acidic solution. An alumina column may also be used to adsorb the cobalt nitroso-R-chelate anion in the presence of perchloric acid, the other elements are eluted with warm 1M nitric acid, and finally the cobalt complex with 1M sulphuric acid, and the absorbance measured at 500 nm. 

Manganese fluoride trioxide, 4295 Manganese tetrafluoride, 4337 Manganese(IV) oxide, 4700 Manganese(VII) oxide, 4704 Mercury(II) bromate, 0269 Mercury(II) nitrate, 4598 Mercury(II) oxide, 4600 Monofluoroxonium hexafluoroarsenate, 0097 Neptunium hexafluoride, 4360 Nickel(II) nitrate, 3583... 

Write the formulas for the following ionic compounds (a) lithium hydride (b) calcium bromate (c)chromium(II) oxide id) thorium(IV) perchlorate (e) nickel phosphate if) zinc sulfate. 

Ignites on contact with metal oxides (e.g., barium peroxide, chromium trioxide, copper oxide, lead dioxide, manganese dioxide, nickel oxide, silver(I) oxide, silver(II) oxide, sodium peroxide, thallium(III) oxide, mercury oxide, calcium oxide, nickel oxide), oxidants (e.g., silver bromate, heptasilver nitrate octaoxide, dibismuth dichromium nonaoxide, mercury(I) bromate, lead(II) hypochlorite, copper chromate, fluorine, nitric acid, sodium peroxide, lead(IV) oxide), rust, soda-lime + air. Reacts violently with NI3, NF3, p-bromobenzenediazonium chloride, OF2, F2, Cu, CIO, BrFs,... 

Under given conditions, passivity is attained with increasing readiness in the order iron, cobalt, nickel iron is much more difficult to render passive than is nickel in a particular electrolyte. Metals of the iron group become passive more readily in alkaline than in acid solutions, and oxidizing agents, e.g., iodate, bromate, chlorate, chromate and nitrate, favor passivity chloride ions markedly inhibit the onset of passivity. Increase of temperature increases the c.d. required for the anode to become passive under a given set of conditions. 

The liberated nickel ion required 26.73 mL of 0.02089 M EDTA. The bromate in a 10.00-mL aliquot was reduced to bromide with arsenic(III) prior to the addition of silver nitrate. The same procedure was followed, and the released nickel ion was titrated with 21.94 mL of the EDTA solution. Calculate the percentages of NaBr and NaBr03 in the sample. 

BENSULFOID (7704-34-9) Combustible solid (flash point 405°F/207°C). Finely divided dry materia forms explosive mixture with air. The vapor reacts violently with lithium carbide. Reacts violently with many substances, including strong oxidizers, aluminum powders, boron, bromine pentafluoride, bromine trifluoride, calcium hypochlorite, carbides, cesium, chlorates, chlorine dioxide, chlorine trifluoride, chromic acid, chromyl chloride, dichlorine oxide, diethylzinc, fluorine, halogen compounds, hexalithium disilicide, lampblack, lead chlorite, lead dioxide, lithium, powdered nickel, nickel catalysis, red phosphorus, phosphorus trioxide, potassium, potassium chlorite, potassium iodate, potassium peroxoferrate, rubidium acetylide, ruthenium tetraoxide, sodium, sodium chlorite, sodium peroxide, tin, uranium, zinc, zinc(II) nitrate, hexahydrate. Forms heat-, friction-, impact-, and shock-sensitive explosive or pyrophoric mixtures with ammonia, ammonium nitrate, barium bromate, bromates, calcium carbide, charcoal, hydrocarbons, iodates, iodine pentafluoride, iodine penloxide, iron, lead chromate, mercurous oxide, mercury nitrate, mercury oxide, nitryl fluoride, nitrogen dioxide, inorganic perchlorates, potassium bromate, potassium nitride, potassium perchlorate, silver nitrate, sodium hydride, sulfur dichloride. Incompatible with barium carbide, calcium, calcium carbide, calcium phosphide, chromates, chromic acid, chromic... 

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