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Platinum analysis

Figure 4 is a back-scattered electron image of the sintered platinum-doped tungsten oxide photocat yst (the bri t spheres are platinum). Analysis of the sintered platinum-doped tungsten oxide by ESCA reveal that the platinum the surface is Pt. ... [Pg.411]

Analysis.—Decomposition in aqueous alkali proved to be unsuitable analytical procedure for dioxygenyl hexafiuoroplatinate(v), giving consistently low values for fluorine. Platinum analysis required two determinations, one of the mixture of metallic platinum and hydrated platinum oxides, the other of the solution of hexafluoroplatinate(iv). The precipitate was reduced to the metal in hydrogen. Platinum in the solution was precipitated by zinc. The total-platinum figures were not very concordant and always higher than that required... [Pg.9]

Wei C and Morrison GM (1994) Platinum analysis and spedation in urban gullypots. Anal Chim Acta 284 213-227. [Pg.50]

The mechanism for CO oxidation over platinum group metals has been established from a wealth of data, the analysis of which is beyond the scope of this chapter. It is quite evident that surface science provided the foundation for this mechanism by directly showing that CO adsorbs molecularly and O2 adsorbs... [Pg.952]

If an appreciable amount of residue remains, note its colour. Add a few drops of water and test the solution (or suspension) with htmus or with Universal indicator paper. Then add a httle dilute hydrochloric acid and observe whether efiervesceiice occurs and the residue dissolves. Apply a flame test with a platinum wire on the hydrochloric acid solution to determine the metal present. (In rare cases, it may be necessary to subject a solution of the residue to the methods of qualitative inorganic analysis to identify the metal or metals present.) If the flame test indicates sodium, repeat the ignition of the substance on platinum foil. [Pg.1038]

Does the platinum working electrode serve as the cathode or the anode in this analysis ... [Pg.506]

The second form consists of Pt metal but the iridium is present as iridium dioxide. Iridium metal may or may not be present, depending on the baking temperature (14). Titanium dioxide is present in amounts of only a few weight percent. The analysis of these coatings suggests that the platinum metal acts as a binder for the iridium oxide, which in turn acts as the electrocatalyst for chlorine discharge (14). In the case of thermally deposited platinum—iridium metal coatings, these may actually form an intermetallic. Both the electrocatalytic properties and wear rates are expected to differ for these two forms of platinum—iridium-coated anodes. [Pg.121]

Color. Many water samples have a yellow to brownish-yeUow color which is caused by natural substances, eg, leaves, bark, humus, and peat material. Turbidity in a sample can make the measurement of color uncertain and is usually removed by centrifiigation prior to analysis. The color is usually measured by comparison of the sample with known concentrations of colored solutions. A platinum—cobalt solution is used as the standard, and the unit of color is that produced by 1 mg/L platinum as chloroplatinate ion. The standard is prepared from potassium chloroplatinate (K PtCl ) and cobalt chloride (C0CI26H2O). The sample may also be compared to suitably caUbrated special glass color disks. [Pg.230]

Thermal Properties. The thermal stabiUty of cellulose esters is deterrnined by heating a known amount of ester in a test tube at a specific temperature a specified length of time, after which the sample is dissolved in a given amount of solvent and its intrinsic viscosity and solution color are deterrnined. Solution color is deterrnined spectroscopically and is compared to platinum—cobalt standards. Differential thermal analysis (dta) has also been reported as a method for determining the relative heat stabiUty of cellulose esters (127). [Pg.258]

II should noi be overlooked that platinum has played a crucial role in ihe development of many branches of science even though the amounts of metal involved may have been small. Reliable Pt crucibles were vital in classical analysis on which the foundations of chemistry were laid. It was also widely used in the development of the electric telegraph, incandescent lamps, and thermionic valves. [Pg.1148]

Rhodium-platinum alloys containing up to 40% Rh are used in the form of wire or ribbon in electrical resistance windings for furnaces to operate continuously at temperatures up to 1 750°C. Such windings are usually completely embedded in a layer of high-grade alumina cement or flame-sprayed alumina to prevent volatilisation losses from the metal due to the free circulation of air over its surface. Furnaces of this type are widely employed for steel analysis, ash fusions and other high-temperature analytical procedures. [Pg.941]

Chemical and catalytic. This grade of platinum is for conversion to catalysts, gauzes and chemical compounds. Spectrographic analysis is employed to control the presence of trace impurities harmful in these applications. [Pg.942]

For the preparation of samples for X-ray fluorescence spectroscopy, lithium metaborate is the preferred flux because lithium does not give rise to interfering X-ray emissions. The fusion may be carried out in platinum crucibles or in crucibles made from specially prepared graphite these graphite crucibles can also be used for the vacuum fusion of metal samples for the analysis of occluded gases. [Pg.113]

From the study of the influencing of single reactions by products and by other added substances and from the analysis of mutual influencing of reactions in coupled systems, the following conclusions can be drawn concerning adsorption of the reaction components. (1) With the exception of crotyl alcohol on the platinum-iron-silica gel catalyst, all the substances present in the coupled system, i.e. reactants, intermediate products, and final products, always adsorbed on the same sites of the catalytic surface (competitive adsorption). This nonspecificity was established also in our other studies (see Section IV.F.2) and was stated also by, for example, Smith and Prater (32), (2) The adsorption of starting reactants and the desorption of the intermediate and final products appeared in our studies always as faster, relative to the rate of chemical transformations of adsorbed substances on the surface of the catalyst. [Pg.49]

A sophisticated quantitative analysis of experimental data was performed by Voltz et al. (96). Their experiment was performed over commercially available platinum catalysts on pellets and monoliths, with temperatures and gaseous compositions simulating exhaust gases. They found that carbon monoxide, propylene, and nitric oxide all exhibit strong poisoning effects on all kinetic rates. Their data can be fitted by equations of the form ... [Pg.91]

Many elements of a mathematical model of the catalytic converter are available in the classical chemical reactor engineering literature. There are also many novel features in the automotive catalytic converter that need further analysis or even new formulations the transient analysis of catalytic beds, the shallow pellet bed, the monolith and the stacked and rolled screens, the negative order kinetics of CO oxidation over platinum,... [Pg.114]

In 1971, a short communication was published [54] by Kumada and co-workers reporting the formation of di- and polysilanes from dihydrosilanes by the action of a platinum complex. Also the Wilkinson catalyst (Ph3P)3RhCl promotes hydrosilation. If no alkenes are present, formation of chain silanes occurs. A thorough analysis of the product distribution shows a high preference for polymers (without a catalyst, disproportionation reactions of the silanes prevail). Cross experiments indicate the formation of a silylene complex as intermediate and in solution, free silylenes could also be trapped by Et3SiH [55, 56],... [Pg.30]


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See also in sourсe #XX -- [ Pg.315 ]




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