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Subject silver

It must be noted, however, that nitroso, azoxy and azo compounds when subjected to the same treatment yield res])ectively hydroxylamines, hydrazo and hydrazine compounds, all of which reduce ammoniacal silver nitrate solution in the cold. [Pg.528]

The use of sensitizing dyes in photography has been the subject of many studies and constitutes. still now. one of the most studied areas in specialized periodic publications (125, 126) or in textbooks (88. 127). It can be ascertained that one hundred years after Vogel s discovery of spectral sensitization, the basic mechanisms of action of dyes on their silver halide support still remain not fully understood. However, the theoretical reasons explaining why among many other dye families practically only cyanine methine dyes appear to be spectral sensitizers (128) are better known. [Pg.78]

Silver electrodes prepared by any of the three methods are almost always subjected to a sintering operation prior to cell or battery assembly. [Pg.554]

Refining. The alloy of bismuth and lead from the separation procedures is treated with molten caustic soda to remove traces of such acidic elements as arsenic and teUutium (4). It is then subjected to the Parkes desilverization process to remove the silver and gold present. This process is also used to remove these elements from lead. [Pg.124]

This is one approach to the explanation of retention by polar interactions, but the subject, at this time, remains controversial. Doubtless, complexation can take place, and probably does so in cases like olefin retention on silver nitrate doped stationary phases in GC. However, if dispersive interactions (electrical interactions between randomly generated dipoles) can cause solute retention without the need to invoke the... [Pg.76]

The choice of the anion ultimately intended to be an element of the ionic liquid is of particular importance. Perhaps more than any other single factor, it appears that the anion of the ionic liquid exercises a significant degree of control over the molecular solvents (water, ether, etc.) with which the IL will form two-phase systems. Nitrate salts, for example, are typically water-miscible while those of hexaflu-orophosphate are not those of tetrafluoroborate may or may not be, depending on the nature of the cation. Certain anions such as hexafluorophosphate are subject to hydrolysis at higher temperatures, while those such as bis(trifluoromethane)sulfonamide are not, but are extremely expensive. Additionally, the cation of the salt used to perform any anion metathesis is important. While salts of potassium, sodium, and silver are routinely used for this purpose, the use of ammonium salts in acetone is frequently the most convenient and least expensive approach. [Pg.35]

Similar remarks apply to the determination of bromides the Mohr titration can be used, and the most suitable adsorption indicator is eosin which can be used in dilute solutions and even in the presence of 0.1 M nitric acid, but in general, acetic (ethanoic) acid solutions are preferred. Fluorescein may be used but is subject to the same limitations as experienced with chlorides [Section 10.77(b)], With eosin indicator, the silver bromide flocculates approximately 1 per cent before the equivalence point and the local development of a red colour becomes more and more pronounced with the addition of silver nitrate solution at the end point the precipitate assumes a magenta colour. [Pg.351]

The reaction is a sensitive one, but is subject to a number of interferences. The solution must be free from large amounts of lead, thallium (I), copper, tin, arsenic, antimony, gold, silver, platinum, and palladium, and from elements in sufficient quantity to colour the solution, e.g. nickel. Metals giving insoluble iodides must be absent, or present in amounts not yielding a precipitate. Substances which liberate iodine from potassium iodide interfere, for example iron(III) the latter should be reduced with sulphurous acid and the excess of gas boiled off, or by a 30 per cent solution of hypophosphorous acid. Chloride ion reduces the intensity of the bismuth colour. Separation of bismuth from copper can be effected by extraction of the bismuth as dithizonate by treatment in ammoniacal potassium cyanide solution with a 0.1 per cent solution of dithizone in chloroform if lead is present, shaking of the chloroform solution of lead and bismuth dithizonates with a buffer solution of pH 3.4 results in the lead alone passing into the aqueous phase. The bismuth complex is soluble in a pentan-l-ol-ethyl acetate mixture, and this fact can be utilised for the determination in the presence of coloured ions, such as nickel, cobalt, chromium, and uranium. [Pg.684]

Potassium peroxodisulphate (K2S2Og) also oxidizes sulphoxides to sulphones in high yield, either by catalysis with silver(I) or copper(II) salts at room temperature85 or in pH 8 buffer at 60-80 °c86-88. The latter conditions have been the subject of a kinetic study, and of the five mechanisms suggested, one has been shown to fit the experimental data best. Thus, the reaction involves the heterolytic cleavage of the peroxodisulphate to sulphur... [Pg.978]


See other pages where Subject silver is mentioned: [Pg.137]    [Pg.137]    [Pg.439]    [Pg.2490]    [Pg.347]    [Pg.291]    [Pg.196]    [Pg.459]    [Pg.459]    [Pg.460]    [Pg.316]    [Pg.516]    [Pg.554]    [Pg.470]    [Pg.471]    [Pg.480]    [Pg.480]    [Pg.481]    [Pg.211]    [Pg.430]    [Pg.32]    [Pg.455]    [Pg.232]    [Pg.503]    [Pg.91]    [Pg.128]    [Pg.287]    [Pg.128]    [Pg.933]    [Pg.944]    [Pg.557]    [Pg.558]    [Pg.560]    [Pg.9]    [Pg.129]    [Pg.150]    [Pg.180]    [Pg.198]    [Pg.118]    [Pg.488]    [Pg.99]    [Pg.108]   
See also in sourсe #XX -- [ Pg.55 ]

See also in sourсe #XX -- [ Pg.49 , Pg.149 , Pg.154 , Pg.158 , Pg.162 , Pg.164 , Pg.193 ]




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Cobaltate -, silver Subject

SILVER SALT Subject

Silver azide Subject

Silver nitrate, reaction with Subject

Silver oxide Subject

Silver perchlorate 412 Subject

Subject silver complexes

Subject silver halides

Subject silver nitrate

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