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Rock salt region

The infrared spectra in the rock-salt region of a comprehensive range of complexes have been tabulated (392, 520, 556, 626, 644). The spectra are very similar with the exception of those of the spin-paired iron(II) complexes (392). The spectra of iron(II) complexes with bipyridyl, phenanthroline, and related a-diimine ligands have been discussed by Busch and Bailar (122). [Pg.159]

Kaye has pointed out that sample cells for the near-infrared region must be many times thicker than those used for conventional (rock-salt region) infrared spectroscopy. Thicknesses of 1, 5, and 10 cm are convenient for most near-infrared work with liquid samples. He recommends the pathlengths shown in Table I for specific applications with liquids in this region. Hamilton s paper on displacement spectrophotometry describes means of using ordinary test tubes in quantitative work. [Pg.250]

Highway. Rock salt, solar salt, and in some cases in Europe, evaporated salt are used to maintain traffic safety and mobiUty during snow and ice conditions in snowbelt regions throughout the world. Sodium chloride melts ice at temperatures down to its eutectic point of —21.12°C. Most snowstorms occur when the temperature is near 0°C, where salt is very effective. More than 40% of dry salt produced in the United States is used for highway deicing. [Pg.186]

Fig. 4-9. This diagram shows the intensity variation with angle for a rock salt crystal in the region near the Bragg angle, 0q, for an incident monochromatic beam. The area under the mosaic crystal curve could be thirty times greater than the ideal. (After Renninger, Z. Krist. 89, 344.)... Fig. 4-9. This diagram shows the intensity variation with angle for a rock salt crystal in the region near the Bragg angle, 0q, for an incident monochromatic beam. The area under the mosaic crystal curve could be thirty times greater than the ideal. (After Renninger, Z. Krist. 89, 344.)...
Normal glass will only transmit radiation between about 350 nm and 3 /rm and, as a result, its use is restricted to the visible and near infrared regions of the spectrum. Materials suitable for the ultraviolet region include quartz and fused silica (Figure 2.28). The choice of materials for use in the infrared region presents some problems and most are alkali metal halides or alkaline earth metal halides, which are soft and susceptible to attack by water, e.g. rock salt and potassium bromide. Samples are often dissolved in suitable organic solvents, e.g. carbon tetrachloride or carbon disulphide, but when this is not possible or convenient, a mixture of the solid sample with potassium bromide is prepared and pressed into a disc-shaped pellet which is placed in the light path. [Pg.70]

An infrared spectrum of a film of peroxide between rock salt plates showed the presence of carbonyl and hydroxyl absorption from decomposition products. There was a wide region of C—O stretching absorption... [Pg.155]

Rg. 4.18 Actual crystal structures of the alkali halides (as shown by the symbols) contrasted with the predictions cl the radius ratio rule. Tie figure is divided into three regions by the lines rjr. 0.414 and r+/h- a 0.732, predicting coordination number 4 (wurizite or zinc blende, upper left), coordination number 6 (rock salt, NaCl, middle), and coordination number 8 (CsCI, lower right). The crystal radius of lithium, and to a lesser extent that of sodium, changes with coordination number, so both ihe radii with C.N. 4 (left) and C.N = 6 Iright) have been plotted. [Pg.75]

Figure 21 Two complete hysteresis cycles for 4.5 mn CdSe NQDs presented as unit cell voliunes for the wurtzite sixfold-coordinated phase (triangles) and the rock-salt fourfold-coordinated phase (squares) versus pressure. Sohd arrows indicate the direction of pressure change, and dotted boxes indicate the mixed-phase regions. Unlike hulk phase transitions, the wurtzite to rock-salt transformation in nanocrystals is reversible and occurs without the formation of new high-energy defects, as indicated by overlapping hysteresis loops. The shape change that a sliding-plane transformation mechanism (see text) would induce is shown schematically on the right. (Reprinted figure with permission from J.N. Wickham, A.B. Herhold, and A.P. Alivisatos, Phys. Rev. Lett., 2000, 84, 923. 2000 by the American Physical Society)... Figure 21 Two complete hysteresis cycles for 4.5 mn CdSe NQDs presented as unit cell voliunes for the wurtzite sixfold-coordinated phase (triangles) and the rock-salt fourfold-coordinated phase (squares) versus pressure. Sohd arrows indicate the direction of pressure change, and dotted boxes indicate the mixed-phase regions. Unlike hulk phase transitions, the wurtzite to rock-salt transformation in nanocrystals is reversible and occurs without the formation of new high-energy defects, as indicated by overlapping hysteresis loops. The shape change that a sliding-plane transformation mechanism (see text) would induce is shown schematically on the right. (Reprinted figure with permission from J.N. Wickham, A.B. Herhold, and A.P. Alivisatos, Phys. Rev. Lett., 2000, 84, 923. 2000 by the American Physical Society)...
Additionally a scale of temperature with depth is given using the mean regional temperature gradient of 33°C/1000 m. The temperatures of 115 and 151°C have been marked in Fig. 7. They confine an anomaly of higher rock salt permeabilities. [Pg.182]

Commercial spectrometers became available in the late 1930s. World War II spurred production of improved spectrometers and development of analytical methods to solve the isomer analysis needs of the petroleum, rubber, and chemical industries. Fortunately, the rock salt prism data obtained during those productive years In the application of infrared spectroscopy to commercial products and complex mixtures are as effective in the fingerprinting region for... [Pg.711]


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