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Reduction elements after

Dendrimers containing Pt " or Pt-metal nanoparticles are easily attached to Au and other surfaces by immersion in a dilute aqueous solution of the composite for 20 h, followed by careful rinsing and drying [59,129]. Therefore it is possible to use X-ray photoelectron spectroscopy (XPS) to determine the elemental composition and the oxidation states of Pt within dendrimers. For example, Pt(4f7/2) and Pt(4f5/2) peaks are present at 72.8 eV and 75.7 eV, respectively, prior to reduction, but after reduction they shift to 71.3 eV and 74.4 eV, respectively, which is consistent with the change in oxidation state from -i-2 to 0 (Fig. 13 a]. [Pg.107]

The traces are precipitated as a hydroxides or acids b - suiphides c - sulphates d -elements after reduction e - 8-hydroxyquinolinates f - silver salts. [Pg.14]

Table 3, Distribution of tracer elements after reduction with Sinz and coprecipitation with Itt PtC in 85% ethanol. (Ref. 17). Table 3, Distribution of tracer elements after reduction with Sinz and coprecipitation with Itt PtC in 85% ethanol. (Ref. 17).
Silicon is the second most abundant element, after oxygen, in Earth s crust. It occvus in Si02 and in an enormous variety of silicate minerals. The element is obtained by the reduction of molten silicon dioxide with carbon at high temperature ... [Pg.950]

When thorium is present with rare earth elements after the breakdown of monazite by sulphuric acid, the solution may be partially neutralized, to pH2, and absorption can take place onto the anion-exchange resin Amber-lite IRA-400. 8 Cerium is the only rare earth element which might absorb appreciably, but this can be prevented by reduction to the cerous state with sodium nitrite first. The thorium is eluted with 2N hydrochloric acid. [Pg.114]

Aluminum is the most abundant metal in the Earth s crust, and the third most abundant element, after oxygen and silicon. It makes up about 8% by weight of the Earth s solid surface. Aluminum metal is too reactive chemically to occur in nature as a metal. Instead, it is found combined in over 270 different minerals [1]. Due to its reactivity, aluminum metal is a modem metal with an annual production currently approaching 40 million tons. Up till the late nineteenth century aluminum metal was considered a pressure metal and most of the metal at that time was produced by metallothermic reduction (K or Na) of anhydrous aluminum chloride (AICI3). [Pg.103]

The standard red-ox potential of tellurium in alkali chloride melts is more positive than that of palladium. Addition of elemental tellurium to NaCl-CsCl-U02Cl2 melt at 550 °C resulted in a quite slow uranium reduction reaction. After 180 min the oxidation state of uranium decreased to 5.92 and the concentration of uranium in the melt from 0.85 to 0.79 wt%. The absorption spectra contained two well pronounced bands corresponding to the uranyl(V) complex, U02Cl4 . [Pg.517]

After oxygen, silicon is the most abundant element in the earth s crust, It occurs extensively as the oxide, silica, in various forms, for example, flint, quartz, sand, and as silicates in rocks and clays, but not as the free element, silicon. Silicon is prepared by reduction of silica, Si02- Powdered amorphous silicon can be obtained by heating dry powdered silica with either powdered magnesium or a... [Pg.165]

L. Holmia, for Stockholm). The special absorption bands of holmium were noticed in 1878 by the Swiss chemists Delafontaine and Soret, who announced the existence of an "Element X." Cleve, of Sweden, later independently discovered the element while working on erbia earth. The element is named after cleve s native city. Holmia, the yellow oxide, was prepared by Homberg in 1911. Holmium occurs in gadolinite, monazite, and in other rare-earth minerals. It is commercially obtained from monazite, occurring in that mineral to the extent of about 0.05%. It has been isolated by the reduction of its anhydrous chloride or fluoride with calcium metal. [Pg.193]

Uranium [7440-61-17 is a naturally occurring radioactive element with atomic number 92 and atomic mass 238.03. Uranium was discovered in a pitchblende [1317-75-5] specimen ia 1789 by M. H. Klaproth (1) who named the element uranit after the planet Uranus, which had been recendy discovered. For 50 years the material discovered by Klaproth was thought to be metallic uranium. Pnligot showed that the uranit discovered by Klaproth was really uranium dioxide [1344-57-6] UO2, and obtained the tme elemental uranium as a black powder in 1841 by reduction of UCl [10026-10-5] with potassium (2). [Pg.313]

The metallized film capacitors have the characteristic of self-healing. On a small dielectric failure the capacitor element is not rendered completely unserviceable. After clearing the fault, the affected capacitor element returns to the circuit and the capacitor unit functions normally. Only the punctured area is eliminated from the element and causes a negligibly small reduction in its capacitance value. Such a characteristic is termed self-healing and such capacitors are known as the self-healing type. [Pg.814]

In 1789 M. H. Klaproth examined pitchblende, thought at the time to be a mixed oxide ore of zinc, iron and tungsten, and showed that it contained a new element which he named uranium after the recendy discovered planet, Uranus. Then in 1828 J. J. Berzelius obtained an oxide, from a Norwegian ore now known as thorite he named this thoria after the Scandinavian god of war and, by reduction of its tetrachloride with potassium, isolated the metal thorium. The same method was subsequendy used in 1841 by B. Peligot to effect the first preparation of metallic uranium. [Pg.1250]

Silicon in the elemental state has important electronic applications as a semiconductor that were developed only during the last decade. The discovery of these uses was possible only after methods were developed for preparing silicon of extremely high purity. Reduction of Si02 with... [Pg.373]

The catalysts formed by the support of organometallic compounds of transition elements are also of great interest for nonpolymerization reactions. Generally speaking, these catalysts can be used in three various states (a) in the initial state, (b) after reduction, and (c) after oxidation... [Pg.191]

Table IV presents the results of the determination of polyethylene radioactivity after the decomposition of the active bonds in one-component catalysts by methanol, labeled in different positions. In the case of TiCU (169) and the catalyst Cr -CjHsU/SiCU (8, 140) in the initial state the insertion of tritium of the alcohol hydroxyl group into the polymer corresponds to the expected polarization of the metal-carbon bond determined by the difference in electronegativity of these elements. The decomposition of active bonds in this case seems to follow the scheme (25) (see Section V). But in the case of the chromium oxide catalyst and the catalyst obtained by hydrogen reduction of the supported chromium ir-allyl complexes (ir-allyl ligands being removed from the active center) (140) C14 of the... Table IV presents the results of the determination of polyethylene radioactivity after the decomposition of the active bonds in one-component catalysts by methanol, labeled in different positions. In the case of TiCU (169) and the catalyst Cr -CjHsU/SiCU (8, 140) in the initial state the insertion of tritium of the alcohol hydroxyl group into the polymer corresponds to the expected polarization of the metal-carbon bond determined by the difference in electronegativity of these elements. The decomposition of active bonds in this case seems to follow the scheme (25) (see Section V). But in the case of the chromium oxide catalyst and the catalyst obtained by hydrogen reduction of the supported chromium ir-allyl complexes (ir-allyl ligands being removed from the active center) (140) C14 of the...
The elemental reaction used to describe a redox reaction is the half reaction, usually written as a reduction, as in the following case for the reduction of oxygen atoms in O2 (oxidation state 0) to H2O (oxidation state —2). The half-cell potential, E°, is given in volts after the reaction ... [Pg.92]


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