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Iron additive lamp

Spectral outputs of some typical metal halide lamps compared to that of the standard mercury lamp mercury barrier discharge lamp (a) mercury barrier discharge lamp, (b) iron additive lamp, and (c) gallium additive lamp. (Courtesy of American Ultraviolet Company.)... [Pg.8]

Tungsten with the addition of as much as 5% thoria is used for thermionic emission cathode wires and as filaments for vibration-resistant incandescent lamps. Tungsten—rhenium alloys are employed as heating elements and thermocouples. Tantalum and niobium form continuous soHd solutions with tungsten. Iron and nickel are used as ahoy agents for specialized appHcations. [Pg.191]

In general, the electrodeless lamp contains a small amount of mercury and a neutral starter gas. The mercury pressures during its operation are in the 5-20 bar range, which is higher than for arc lamps, with pressures only in the 1-2 bar range. The characteristics of fhe lamp can be modified by fhe addition of mefal halides in confrolled quanfifies to the gas. The frequently used D or V lamps contain iron or gallium salts, respectively. Some characteristics of microwave-powered lamps are in Table 3.1. [Pg.24]

Photolysis is a convenient route - to iron carbonyl derivatives using FefCO), and this route may be better than oxidative addition to Fej(CO),2. One illustration is the 1 1 reaction of FefCO), with (Me2GeH)20 under mercury lamp irradiation for 1 h. in pentane to produce ... [Pg.334]

All materials used in the construction of a source can contribute to the resultant spectrum emitted by that lamp. Moreover, these materials, some present at very low parts per million, can have either a transitory or permanent effect on the resultant spectrum. Some of these, e.g., the presence of iron or addition of cerium or titanium to glasses, have produced safer and/or more useful (self-cleaning) lamps. [Pg.88]

Figure 10 Percentage of phenol formed for 0.57 mM drug A in pH 6 10 mM citrate butter after exposing to International Conference on Harmonization visible lamp (1.2 x 10 Lux hour) in the presence of varying concentrations of added iron. The level of iron present in the unspiked sample was determined by a standard addition method as 45 ppb (dashed line, Table 5). Figure 10 Percentage of phenol formed for 0.57 mM drug A in pH 6 10 mM citrate butter after exposing to International Conference on Harmonization visible lamp (1.2 x 10 Lux hour) in the presence of varying concentrations of added iron. The level of iron present in the unspiked sample was determined by a standard addition method as 45 ppb (dashed line, Table 5).
The method is essentially the same as that described in synthesis A. The quantities of bis(trimethylsilyl)amine (0.10 mole) and butyllithium (0.093 mole) are again used, but the solvent is 100 mL of dry benzene (sodium-dried and distilled from calcium hydride). The addition of the anhydrous FeCls (9.8 g, 0.06 mole) leads to a slight warming of the reaction mixture. After 24 hours of stirring at room temperature, by which time the solution has assumed a dark-green coloration, the contents are briefly heated to reflux with an infrared lamp and the mixture is filtered. Concentration of the filtrate produces a mass of dark-green needle crystals, which are filtered, washed with a small amount of cold benzene, pumped dry, and sealed into ampules under vacuum. The yield of tris-[bis(trimethylsilyl)amido]iron(III) is about 10 g (62%). Satisfactory analyses have not been obtained due to this compound s high reactivity to air and moisture. [Pg.119]

USE As alloy with copper and iron in titanium bronze as addition to steel to impart great tensile strength to aluminum to impart resistance to attack by salt solns and by organic acids to remove traces of oxygen and nitrogen from incandescent lamps, Surgical aid (fracture fixation). [Pg.1492]

The addition is accelerated by irradiation (500-w lamp, UV) and radical-formers. Catalysts such as iron, iron chloride, antimony chloride, and iodine favor substitution by chlorine and so must be excluded. The reaction is exothermic and the temperature must be kept at 50-60° by cooling. The /7-isomer is the predominant product when it crystallizes out the reaction is broken off, unchanged benzene is removed, and the mixture of isomers is treated with about its own weight of methanol. The a- and /7-isomer are relatively insoluble in methanol, and the y-isomer crystallizes when the extract is concentrated. [Pg.117]


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See also in sourсe #XX -- [ Pg.8 ]




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