Ammonium Acetate Molybdate

AMMO 2.5 EC , cypermetlu-in, 13 Ammonia, 13 Ammonium acetate, 13 Ammonium arsenate, 13 Ammonium benzoate, 13 Ammonium bicarbonate, 13 Ammonium bifluoride, 14 Ammonium bisulfite, 14 Ammonium carbamate, 14 Ammonium carbonate, 14 Ammonium chloride, 14 Ammonium chlorplatmate, 14 Ammonium clu omate, 14 Ammonium citrate, 14 Ammonium diclu omate, 14 Ammonium fluoride, 14 Ammonium fomiate, 15 Ammonium hexafluorosilicate, 15 Ammonium hydroxide, 15 Ammonium metavanadate, 15 Ammonium molybdate, 15 Ammonium nitrate, 15 Ammonium oxalate, 15 Ammonium perfluorooctanoate, 15 Ammonium persulfate, 15 Ammonium phosphate, 15 Ammonium picrate, 16 Ammonium salicylate, 16... [Pg.321]

Ammonium acetate Ammonium adipate Ammonium benzoate Ammonium bicarbonate Ammonium biflluoride Ammonium binoxalate Ammonium bisulfate Ammonium bitartrate Ammonium tetraborate Ammonium bromide Ammonium carbonate Ammonium chloride Ammonium citrate Ammonium diclnomate Ammonium fluoride Ammonium fluorosilicate Ammonium gluconate Ammonium iodide Ammonium molybdate Ammonium nitrate Ammonium oxalate Ammonium perchlorate Ammonium picrate Ammonium polysulfide Ammonium salicylate Ammonium stearate Ammonium sulfate Ammonium sulfide (hydrosulfide) Ammonium tartrate Ammonium tliiocyanate Ammonium thiosulfate... [Pg.262]

Chemical deposition of both M0S2 and MoSei has been reported from ammonium molybdate solution [76,77], For the sulphur and selenium sources, thioacetamide and selenosulphate were used, respectively. Ammonium hydroxide was added to the sulphide solution, while an acetic acid/ammonium acetate buffer was used with the selenide solution (pH values were not given). Reducing agents (either hydrazine [76] or sodium dithionite [77]) were added to the baths. Deposition was started at 90-100°C, followed by lowering to room temperature. [Pg.247]

Synonym Ammonia Water Amfbnioformaldehyde Ammonium Acetate Ammonium Acid Fluoride Ammonium Amidosulfonate Ammonium Amidosulphate Ammonium Benzoate Ammonium Bicarbonate Ammonium Bichromate Ammonium Bifluoride Ammonium Carbonate Ammonium Chloride Ammonium Citrate Ammonium Citrate, Dibasic Ammonium Decaborate Octahydrate Ammonium Dichromate Ammonium Disulfate-Nickelate (II) Ammonium Ferric Citrate Ammonium Ferric Oxalate Trihydrate Ammonium Ferrous Sulfate Ammonium Fluoride Ammonium Fluosilicate Ammonium Formate Ammonium Gluconate Ammonium Hydrogen Carbonate Ammonium Hydrogen Fluoride Ammonium Hydrogen Sulfide Solution Ammonium Hydroxide Ammonium Hypo Ammonium Hyposulfite Ammonium Iodide Ammonium Iron Sulfate Ammonium Lactate Ammonium Lactate Syrup Ammonium Lauryl Sulfate Ammonium Molybdate Ammonium Muriate Ammonium Nickel Sulfate Ammonium Nitrate Ammonium Nitrate-Urea Solution Ammonium Oleate... [Pg.21]

Ammonium molybdate, when added in considerable excess to a boiling solution of an arsenate in nitric acid, gives a yellow crystalline precipitate of ammonium 12-molybdo-arsenate, (NH4)3H4[As(Mo207)6]. 4H20 (see p. 215). Like the corresponding molybdo-phosphate, the precipitate is readily soluble in ammonia or aqueous alkali. The arsenate may be detected in the presence of phosphate by boiling the yellow precipitate with aqueous ammonium acetate until clear a white precipitate or turbidity on cooling shows the presence of arsenate, and the filtrate may be tested for phosphate.1... [Pg.311]

If metallic tin is fumed with ammonium bromide, volatile stannous bromide results. The latter can be identified by the immediate blue color (molybdenum blue) that forms on treatment with ammonium molybdate or, better, with a solution of phosphomolybdic acid that has been decolorized with excess ammonium acetate. [Pg.481]

Aluminum chloride, 26% Aluminum hydroxide Aluminum nitride Ammonia, dry vapor Ammonium acetate solution Ammonium bisulfate Ammonium bromide Ammonium carbonate Ammonium chloride, 10% Ammonium dichloride Ammonium hydroxide Ammonium hydroxide vapor Ammonium molybdate Ammonium nitrate Argon... [Pg.635]

Aminoethanol 2-Aminoisobutyric Acid Ammonia Ammonia Solution Ammonium Ammonium Acetate Ammonium Alum Ammonium Bicarbonate Ammonium Bichromate Ammonium Bifluoride Ammonium Bromide Ammonium Carbonate Ammonium Chloride Ammonium Dichromate Ammonium Fluoride Ammonium Glycolate Ammonium Hydrogen Carbonate Ammonium Hydrogen Fluoride Ammonium Hydrosulfide Ammonium Hydroxide Ammonium Hyposulfite Ammonium Iron Sulfate Ammonium Molybdate Ammonium m-Phosphate Ammonium Nitrate Ammonium o-Phosphate Ammonium Oxalate Ammonium Peroxydisulfate Ammonium Persulfate Ammonium Phosphate Ammonium Phosphate Dibasic Ammonium Rhodanide Ammonium Sulfamate Ammonium Sulfate Ammonium Sulfide Ammonium Thiocyanate Ammonium Thioglycolate Ammonium Thiosulfate... [Pg.3472]

Column (10) Indicates that volatile material Is aspirated into the huhhler C containing a 10 per cent aqueous solution ot ammonium molybdate mixed with an equal volume of benzidine solution (made by dissolving 0 05 g. of benzidine in 10 ml. of glacial acetic acid and making up to 100 ml. with water). D.F.P. and tabun are hydrolysed to phosphate and a typical green or green-blue coloration is produced.1... [Pg.227]

Procedure (determination of inorganic phosphate (a) in the acetic acid extract). The 8-hydroxyquinoline forms a precipitate in acidic ammonium molybdate solution, which will interfere unless the aliquot is <5 ml. It should therefore be removed by ignition as follows. Transfer 10 ml acetic acid extract to a 45-ml silica basin, add 0.5 ml 1 M magnesium acetate and evaporate to dryness on a water-bath. (Note do not use magnesium nitrate, which reacts adversely on heating with 8-hydroxyquinoline.)... [Pg.195]

The tetrasulfo-Pc complexes of a number of metals are made by the urea melt process by heating the powdered metal, or its acetate, with triammonium-4-sulfophthalate, urea, boric acid, and ammonium molybdate. The metals or metal compounds used are those of chromium (III), manganese(II), iron(II), iron(III), cobalt(II), and zinc(II). Selected synthetic examples of sulfo- and other derivatives of metal phthalocyanines are presented below. [Pg.400]

The precipitates obtained with magnesia mixture (magnesium chloride in ammoniacal solution), or ferric chloride in an acid solution to which sodium acetate has been added, are often used as tests for phosphate (see p. 180), and in the latter case the phosphate is removed from solution as ferric phosphate. Another common test is the formation of yellow ammonium phosphomolybdate when, a nitric acid solution of ammonium molybdate is added to phosphate solution (see pp. 180, 181). [Pg.179]