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A-Platinum

Carboplatin is a promising second-generation platinum agent. Because it is less reactive, it causes less nephrotoxicity, myelosuppression, and thrombocytopenia. [Pg.117]


Spatial Resolution or Unsharpness The total resolution of the system is to be established via a platinum duplex wire penetrameter according to EN 462-5. The resolution limit that has been determined by this IQI can be directly converted to the system unsharpness. [Pg.438]

Fig. VIII-2. Scanning tunneling microscopy images illustrating the capabilities of the technique (a) a 10-nm-square scan of a silicon(lll) crystal showing defects and terraces from Ref. 21 (b) the surface of an Ag-Au alloy electrode being electrochemically roughened at 0.2 V and 2 and 42 min after reaching 0.70 V (from Ref. 22) (c) an island of CO molecules on a platinum surface formed by sliding the molecules along the surface with the STM tip (from Ref. 41). Fig. VIII-2. Scanning tunneling microscopy images illustrating the capabilities of the technique (a) a 10-nm-square scan of a silicon(lll) crystal showing defects and terraces from Ref. 21 (b) the surface of an Ag-Au alloy electrode being electrochemically roughened at 0.2 V and 2 and 42 min after reaching 0.70 V (from Ref. 22) (c) an island of CO molecules on a platinum surface formed by sliding the molecules along the surface with the STM tip (from Ref. 41).
Hydrazine is prepared, anhydrous and in good yield, by glow discharge electrolysis of liquid ammonia a platinum cathode is immersed in liquid and a platinum wire anode is mounted just... [Pg.223]

On a large scale, hydrogen peroxide is produced by the electrolysis of ammonium hydrogensulphate, using a platinum anode and a lead cathode separated by a diaphragm. The essential process occurring is ... [Pg.278]

In the laboratory it is commonly prepared by the reaction between sulphur dioxide and oxygen at high temperature in the presence of a platinum catalyst ... [Pg.295]

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]

Catalytic reduction over a platinum catalyst fails because of poisoning of the catalyst (101). [Pg.535]

Alkenes react with hydrogen in the presence of a platinum palladium rhodium or nickel catalyst to form the corresponding alkane... [Pg.272]

Variations in the Force Due to Gravity. The mass of an object is the quantity of matter ia the object. It is a fundamental quantity that is fixed, and does not change with time, temperature, location, etc. The standard for mass is a platinum—iridium cylinder, called the International Kilogram, maintained at the International Bureau of Weights and Measures, ia Snvres, France. The mass of this cylinder is 1 kg by definition (9). AH national mass standards are traceable to this artifact standard. [Pg.330]

Olefins add anhydrous acetic acid to give esters, usually of secondary or tertiary alcohols propjiene [115-07-1] yields isopropyl acetate [108-21-4], isobutjiene [115-11-7] gives tert-huty acetate [540-88-5]. Minute amounts of water inhibit the reaction. Unsaturated esters can be prepared by a combined oxidative esterification over a platinum group metal catalyst. Eor example, ethylene-air-acetic acid passed over a palladium—Hthium acetate catalyst yields vinyl acetate. [Pg.66]

Preparation and Manufacture. Fluorosulfuric acid, first prepared by combining anhydrous HF and cooled, anhydrous SO in a platinum container (1), has also been prepared from ionic fluorides or fluorosulfates and sulfuric acid (20,48). The reaction of chlorosulfuric acid (qv) with ionic fluorides also gives fluorosulfuric acid (49). [Pg.249]

Pyrolytic routes to hexafluorobenzene have also attracted attention but have not been commercialized. Pyrolysis of tribromofluoromethane [353-54-8] CBr F, at 630—640°C in a platinum tube gives hexafluorobenzene in 55% yield (251—253). The principal disadvantage of this process is the low weight yield of product 90% of the costly CBr F that is charged is lost as bromine. Of economic potential is the related copyrolysis of dichlorofluoromethane [754-34-0] and chlorofluoromethane [593-70-4] (254,255). [Pg.328]

In this pyrolysis, sub atmospheric partial pressures are achieved by employing a diluent such as steam. Because of the corrosive nature of the acids (HE and HCl) formed, the reactor design should include a platinum-lined tubular reactor made of nickel to allow atmospheric pressure reactions to be mn in the presence of a diluent. Because the pyrolysate contains numerous by-products that adversely affect polymerization, the TFE must be purified. Refinement of TFE is an extremely complex process, which contributes to the high cost of the monomer. Inhibitors are added to the purified monomer to avoid polymerization during storage terpenes such as t7-limonene and terpene B are effective (10). [Pg.348]

Quantitative estimation of cyclohexane in the presence of benzene and aUphatic hydrocarbons may be accompHshed by a nitration-dehydrogenation method described in Reference 61. The mixture is nitrated with mixed acid and under conditions that induce formation of the soluble mononitroaromatic derivative. The original mixture of hydrocarbons then is dehydrogenated over a platinum catalyst and is nitrated again. The mononitro compounds of the original benzene and the benzene formed by dehydrogenation of the cyclohexane dissolve in the mixed acid. The aUphatic compound remains unattacked and undissolved. This reaction may be carried out on a micro scale. [Pg.409]

C. HIO is prepared by oxidation of iodine with perchloric acid, nitric acid, or hydrogen peroxide or oxidation of iodine in aqueous suspension to iodic acid by silver nitrate. Iodic acid is also formed by anodic oxidation at a platinum electrode of iodine dissolved in hydrochloric acid (113,114). [Pg.365]

Platinum—Iridium. There are two distinct forms of 70/30 wt % platinum—iridium coatings. The first, prepared as prescribed in British patents (3—5), consists of platinum and iridium metal. X-ray diffraction shows shifted Pt peaks and no oxide species. The iridium [7439-88-5] is thus present in its metallic form, either as a separate phase or as a platinum—iridium intermetallic. The surface morphology of a platinum—iridium metal coating shown in Figure 2 is cracked, but not in the regular networked pattern typical of the DSA oxide materials. [Pg.121]

Conversion of Ammonia. Ammonia [7664 1-7] mixed with air and having an excess of oxygen, is passed over a platinum catalyst to form nitric oxide and water (eq. 10). The AH g = —226 kJ/mol of NH consumed (—54 kcal/mol). Heats of reaction have been derived from heats of... [Pg.42]

The most significant PGM deposit in the United States is at Stillwater, Montana, where PGMs are mined as the primary product. The grade has been estimated as between 13 and 22 g/1, having a platinum—palladium ratio of 1 3.5. The first ore was extracted from Stillwater in 1987 and full production of 1000 t/d was reached in 1990. [Pg.166]

Miscellaneous. Chloroplatinic acid is used in the production of automobile catalysts. Platino-type prints based on reduction of Pt(II) to Pt(0) by a photosensitive reducing agent such as iron(III) oxalate are used in art photography (261,262). Infrared imaging devices based on a platinum siLicide detector have been developed (263). [Pg.185]


See other pages where A-Platinum is mentioned: [Pg.71]    [Pg.77]    [Pg.290]    [Pg.294]    [Pg.348]    [Pg.294]    [Pg.517]    [Pg.599]    [Pg.1908]    [Pg.2708]    [Pg.98]    [Pg.323]    [Pg.628]    [Pg.870]    [Pg.1037]    [Pg.1093]    [Pg.1094]    [Pg.100]    [Pg.258]    [Pg.502]    [Pg.50]    [Pg.146]    [Pg.503]    [Pg.235]    [Pg.358]    [Pg.310]    [Pg.374]    [Pg.477]    [Pg.495]    [Pg.28]    [Pg.41]    [Pg.42]   


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A Descriptive Model of Hydrocarbon Catalysis on Platinum Surfaces

A Linear Dimetallic Platinum Complex

Ethanol at a Platinum Electrode

Face-Centered Cubic Platinum as a Catalyst

Formation of Platinum—Pyrimidine and a-Pyridone Blues

Hydrogenation, of a double bond over platinum

Methanol at a Platinum Electrode

Photoinduced Surface Dynamics of CO Adsorbed on a Platinum Electrode

Platinum (s. a. Chloroplatinic

Platinum Alloys and Composites as Catalysts for Anodes

Platinum Anticancer Prodrugs A Photoactivation Strategy

Platinum Complexes Suitable as Precursors for Synthesis in Nonaqueous Solvents

Platinum as electrocatalyst

Platinum as electrodes

Platinum, as catalyst

Platinum-Carbon a-Bonds

Platinum-amine complexes as trypanocides

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