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Cupferron

Cupferron, the ammonium salt of the N-nitroso derivative of phenylhydr-oxylamine, is prepared by passing ammonia gas into an ethereal solution of phenylhydroxylamine and n butyl nitrite  [Pg.957]

It is used in quantitative analysis as a reagent for copper and iron. [Pg.957]


NH4][ON(NO)C6Hj]. a reagent originally suggested for use in the detection of Cu but now used for the separation of Fe/Ti and Zr which it precipitates from acid solutions. Cupferron is a brownish-while crystalline substance, soluble in water. [Pg.118]

Cupferron (iron analysis) dissolve 6 g of ammonium nitrosophenyl-hydroxylamine (cupferron) in water and dilute to 100 mL. This solution is stable for about one week if protected from light. [Pg.1190]

Cupferron is a ligand whose strong affinity for metal ions makes it useful as a chelating agent in liquid-liquid extractions. The following distribution ratios are known for the extraction of Hg +, Pb +, and Zn + from aqueous solutions to an organic solvent. [Pg.230]

CuO 2Co203 6H20 Cupel furnace Cupellation Cupferron... [Pg.265]

A number of organic compounds, eg, acetylacetone [123-54-6] and cupferron [135-20-6] form compounds with aqueous actinide ions (IV state for reagents mentioned) that can be extracted from aqueous solution by organic solvents (12). The chelate complexes are especially noteworthy and, among these, the ones formed with diketones, such as 3-(2-thiophenoyl)-l,l,l-trifluoroacetone [326-91-0] (C4H2SCOCH2COCF2), are of importance in separation procedures for plutonium. [Pg.220]

Many compounds capable of chelation have been tested for antimicrobial properties. Those showing positive results include saHcylaldoxime [94-67-7] l-nitroso-2-naphthol [131-91-9] mercaptobenzothiazol [149-30-4], dimethylglyoxime [95-45-4], saHcylaldehyde [90-02-8], cupferron [135-20-6], phenanthroline [66-71-7], isoniazid [54-85-3], thiosemicarbazones, the sulfur analogue of oxine, and numerous antibiotics (qv) including tetracyclines. Whether these compounds function exclusively, partially, or at all by virtue of their abiHty to chelate is open to debate. [Pg.131]

Cupferron (ammonium salt of N-nitroso-A -phenylhydroxylamine). The reagent is used in cold aqueous solution (about 6 per cent). Metal cupferrates are soluble in diethyl ether and in chloroform, and so the reagent finds wide application in solvent-extraction separation schemes. Thus Fe(III), Ti, and Cu may be extracted from 1.2 M HC1 solution by chloroform numerous other elements may be extracted largely in acidic solution. [Pg.170]

The cupferron method is very satisfadory for the separation of iron, titanium, zirconium, vanadium and, in spedal cases, tin, tantalum, uranium, and gallium. [Pg.440]

The name cupferron was assigned to the compound by O. Baudisch, and is derived from the fact that the reagent precipitates both copper and iron. Cupferron precipitates iron completely in strong mineral-acid solution, and copper is only quantitatively precipitated in faintly acid solution. The selectivity of the reagent is greatest in strongly acid solution. [Pg.440]

Determination of uranium with cupferron Discussion. Cupferron does not react with uranium(VI), but uranium(IV) is quantitatively precipitated. These facts are utilised in the separation of iron, vanadium, titanium, and zirconium from uranium(VI). After precipitation of these elements in acid solution with cupferron, the uranium in the filtrate is reduced to uranium(IV) by means of a Jones reductor and then precipitated with cupferron (thus separating it from aluminium, chromium, manganese, zinc, and phosphate). Ignition of the uranium(IV) cupferron complex affords U308. [Pg.471]

Cupferron. Tin (IV) (ca 150 mg in 300 mL). Add 3 g of boric acid, 2.5 mL of concentrated sulphuric acid (CARE) and finally an excess of 10 per cent aqueous solution of cupferron. Stir vigorously, filter (Whatman No. 41 or 541 filter paper) and wash the precipitate with cold water. Dry the precipitate and filter paper in a weighed crucible, ignite carefully and weigh as Sn02 (Section 11.45). [Pg.474]

Procedure. Dissolve a suitable weight of the sample of lead in 6M nitric acid add a little 50 per cent aqueous tartaric acid to clear the solution if antimony or tin is present. Cool, transfer to a separatory funnel, and dilute to about 25 mL. Add concentrated ammonia solution to the point where the slight precipitate will no longer dissolve on shaking, then adjust the pH to 1, using nitric acid or ammonia solution. Add 1 mL freshly prepared 1 per cent cupferron solution, mix, and extract with 5 mL chloroform. Separate the chloroform layer, and repeat the extraction twice with 1 mL portions of cupferron solution + 5 mL of chloroform. Wash the combined chloroform extracts with 5mL of water. Extract the bismuth from the chloroform by shaking with two 10 mL portions of 1M sulphuric acid. Run the sulphuric acid solution into a 25 mL graduated flask. Add 3 drops saturated sulphur dioxide solution and 4 mL of 20 per cent aqueous potassium iodide. Dilute to volume and measure the transmission at 460 nm. [Pg.685]

Molybdenum(VI), vanadium(V), mercury, and iron interfere permanganates, if present, may be removed by boiling with a little ethanol. If the ratio of vanadium to chromium does not exceed 10 1, nearly correct results may be obtained by allowing the solution to stand for 10-15 minutes after the addition of the reagent, since the vanadium-diphenylcarbazide colour fades fairly rapidly. Vanadate can be separated from chromate by adding oxine to the solution and extracting at a pH of about 4 with chloroform chromate remains in the aqueous solution. Vanadium as well as iron can be precipitated in acid solution with cupferron and thus separated from chromium (III). [Pg.687]

If there is any doubt concerning the purity of the potassium titanyl oxalate, standardise the solution by precipitating the titanium with ammonia solution or with cupferron solution, and igniting the precipitate to TiOz. [Pg.697]

Vitreosil filtering, 103 see also Platinum apparatus Crushing and grinding 155 Crystal violet indicator, 308 Cupferron 170, 440, 471, 474 Cupron 442, 473 Current adsorption, 616 catalytic, 616 condenser, 595 diffusion, 592, 596 efficiency, 504 kinetic, 616... [Pg.861]

Cupferron Nitroso-R-salt 688 Nitrous acid removal of. 514 Nonaqueous titrations 307 indicators for, 284 solvents for. 283... [Pg.869]


See other pages where Cupferron is mentioned: [Pg.33]    [Pg.118]    [Pg.630]    [Pg.957]    [Pg.957]    [Pg.1144]    [Pg.1144]    [Pg.1144]    [Pg.1188]    [Pg.1213]    [Pg.249]    [Pg.734]    [Pg.265]    [Pg.224]    [Pg.446]    [Pg.25]    [Pg.134]    [Pg.366]    [Pg.60]    [Pg.65]    [Pg.47]    [Pg.132]    [Pg.440]    [Pg.440]    [Pg.440]    [Pg.471]    [Pg.821]    [Pg.822]   
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Actinide complexes cupferron

Antimony complexes cupferron

Copper complexes cupferron

Copper cupferronate

Cupferron complexes

Cupferron extraction

Cupferron metal complexes

Cupferron uranium complexes

Iron cupferronate

Iron cupferronate structure

Metal-cupferron decomposition

Neptunium complexes cupferron

Organic reagents cupferron

Plutonium complexes cupferron

Protactinium complexes cupferron

Technetium complexes cupferron

Titanium complexes cupferron

Uranyl complexes cupferron

Vanadium complexes cupferron

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