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Gallium, pure

Besides stmctural variety, chemical diversity has also increased. Pure silicon fonns of zeolite ZSM-5 and ZSM-11, designated silicalite-l [19] and silicahte-2 [20], have been synthesised. A number of other pure silicon analogues of zeolites, called porosils, are known [21]. Various chemical elements other than silicon or aluminium have been incoriDorated into zeolite lattice stmctures [22, 23]. Most important among those from an applications point of view are the incoriDoration of titanium, cobalt, and iron for oxidation catalysts, boron for acid strength variation, and gallium for dehydrogenation/aromatization reactions. In some cases it remains questionable, however, whether incoriDoration into the zeolite lattice stmcture has really occurred. [Pg.2782]

Ultra-pure gallium has a beautiful, silvery appearance, and the solid metal exhibits a conchoidal fracture similar to glass. The metal expands 3.1 percent on solidifying therefore, it should not be stored in glass or metal containers, because they may break as the metal solidifies. [Pg.87]

It is available in ultra pure form. Indium is a very soft, silvery-white metal with a brilliant luster. The pure metal gives a high-pitched "cry" when bent. It wets glass, as does gallium. [Pg.116]

The water elimination reactions of Co3(P04)2 8 H20 [838], zirconium phosphate [839] and both acid and basic gallium phosphates [840] are too complicated to make kinetic studies of more than empirical value. The decomposition of the double salt, Na3NiP3O10 12 H20 has been shown [593] to obey a composite rate equation comprised of two processes, one purely chemical and the other involving diffusion control, for which E = 38 and 49 kJ mole-1, respectively. There has been a thermodynamic study of CeP04 vaporization [841]. Decomposition of metal phosphites [842] involves oxidation and anion reorganization. [Pg.185]

Arsenic and antimony are metalloids. They have been known in the pure state since ancient times because they are easily obtained from their ores (Fig. 15.3). In the elemental state, they are used primarily in the semiconductor industry and in the lead alloys used as electrodes in storage batteries. Gallium arsenide is used in lasers, including the lasers used in CD players. Metallic bismuth, with its large, weakly bonded atoms, has a low melting point and is used in alloys that serve as fire detectors in sprinkler systems the alloy melts when a fire breaks out nearby, and the sprinkler system is activated. Like ice, solid bismuth is less dense than the liquid. As a result, molten bismuth does not shrink when it solidifies in molds, and so it is used to make low-temperature castings. [Pg.745]

Silicon is not as prominent a material in optoelectronics as it is in purely electronic applications, since its optical properties are limited. Yet it finds use as a photodetector with a response time in the nanosecond range and a spectral response band from 0.4 to 1.1 im, which matches the 0.905 im photoemission line of gallium arsenide. Silicon is transparent beyond 1.1 im and experiments have shown that a red light can be produced by shining an unfocused green laser beam on a specially prepared ultrathin crystal-silicon slice.CVD may prove useful in preparing such a material. [Pg.386]

For relatively simple matrices, such as pure metallic CRMs synthetic reference materials for direct calibration were prepared and used, for example Bi, Cd, Hg, Pb and T1 in high purity gallium (HUtenkamp and Jackwerth 1988), Ag in copper (Pau-wels et al. 1990) and Au and Pd in silver (Hinds 1993). Direct calibration by solid biological materials with added analyte belongs also to these quite successfully applied techniques (Hofmarm et al. 1992). [Pg.139]

On the other hand, Li and Wang recently developed a highly efficient asymmetric Mukaiyama reaction by using chiral gallium catalysts with Trost s chiral semicrown ligands (Eq. 8.106).287 Such a system can achieve high enantioselectivity even in pure water. The combination... [Pg.274]

Leite, R. C. C. DiGiovanni, A. E. 1967. Frequency shift with temperature as evidence for donor-acceptor pair recombination in relatively pure n-type gallium arsenide. Phys. Rev. 153 841-843. [Pg.198]

Sulphide-type phosphors are produced from pure zinc or cadmium sulphide (or mixtures thereof) and heating them together at about 1000 °C with small quantities (0.1-0.001 per cent) of copper, silver, gallium, or other salts, which are termed activators. [Pg.477]

J. Qiao, Y. Qiu, L. Wang, L. Duan, Y. Li, and D. Zhang, Pure red electroluminescence from a host material of binuclear gallium complex, Appl. Phys. Lett., 81 4913 1915 (2002). [Pg.405]

In contrast to the non-trivial routes for the syntheses of pure aluminum(I) or gallium(I) subhalides, indium(I) chloride or bromide can simply be prepared by melting mixtures of elemental indium and indium trihalides [39]. When these in-dium(I) halides were treated with bulky alkyllithium compounds, deep violet orga-noelement indium dusters (13-18) were obtained [Eq. (3)] [40, 41]. [Pg.131]

The lack of a single ordering principle is a shortcoming particularly for the gallium clusters, since there are a larger number of them compared with the corresponding aluminum clusters as a result of their improved synthesis procedures (cf. Section 2.3.3). A purely formal means of classification for the gallium clusters... [Pg.151]

Several other analytical procedures exist in which solvent extraction may be applied. Thus extraction has been used in a limited number of analyses with procedures such as (1) luminescence (fluorimetry), where, for example, the detection limit of rhodamine complexes of gallium or indium can be increased by extraction [28] (2) electron spin resonance using a spin-labelled extractant [29] and (3) mass spectrometry, where an organic extract of the analyte is evaporated onto pure AI2O3 before analysis [30]. [Pg.571]

Gallium antimonide (GaSb), when in pure form, is used in semiconductor industries. [Pg.183]

Overall, the UV-visible, NMR, and electrochemical data for the range of O -bonded complexes of gallium, indium, and thallium porphyrins show that there is a trend from pure a -bonded character of the M—C bond in the alkyl complexes to the much more ionic character observed for the fluorophenyl and acetylide complexes. These more ionic complexes show NMR and UV-visible characteristics more like those of the ionic M(Por)Cl or M(Por)C104 complexes. ... [Pg.305]

Indium, unlike germanium, is found in zinc blendes which are geologically old. Whereas cadmium occurs mainly in the well-formed crystals of pure zinc blende, indium is found in the fine-grained mixtures in thin ramifying cracks (84). Professor Georges Urbain found that blendes rich in germanium are usually rich also in gallium put poor in indium (84, 87). [Pg.647]

Although gallium sulfide does not precipitate from a solution of the pure salt, it is readily carried down with zinc sulfide. Boisbaudran therefore added ammonium acetate and acetic acid to the hydrochloric acid solution of the above precipitate, and passed in hydrogen sulfide. As long as the line Ga a (417 0) continued to show in the spectrum of the precipitate, he kept on adding zinc to the filtrate until finally all the gallium had been precipitated. [Pg.674]

Other framework structures based on zeolites have also been synthesized which contain atoms other than aluminium and silicon, such as boron, gallium, germanium, and phosphorus, which are tetrahedrally coordinated by oxygen. Such compounds are known as zeotypes. Pure aluminium phosphate, commonly called ALPO, and its derivatives, can take the same structural forms as some of the zeolites such as sodalite (SOD), faujasite (FAU), and chabazite (CHA) (e.g., ALPO-20 is isostructural... [Pg.334]


See other pages where Gallium, pure is mentioned: [Pg.202]    [Pg.140]    [Pg.159]    [Pg.164]    [Pg.118]    [Pg.425]    [Pg.304]    [Pg.62]    [Pg.41]    [Pg.621]    [Pg.12]    [Pg.62]    [Pg.67]    [Pg.357]    [Pg.385]    [Pg.140]    [Pg.279]    [Pg.182]    [Pg.119]    [Pg.43]    [Pg.166]    [Pg.722]    [Pg.304]    [Pg.417]    [Pg.216]    [Pg.28]    [Pg.49]   
See also in sourсe #XX -- [ Pg.26 ]

See also in sourсe #XX -- [ Pg.26 ]

See also in sourсe #XX -- [ Pg.26 ]

See also in sourсe #XX -- [ Pg.26 ]

See also in sourсe #XX -- [ Pg.26 ]




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