Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Sodium frequencies

At the sodium frequency, the optical rotation is rather small for most molecules. However, the individual diagonal elements of the mixed electric dipole-magnetic dipole polarizability maybe fairly large in absolute value, often canceling each other in the trace. This is illustrated for a few selected molecules in O Table 11-7. Consequently, the optical rotation is highly sensitive to numerical errors in the tensor components, because small residual errors in the individual tensor components, arising from the solution of the linear response equations, may lead to substantial errors in Another consequence of this cancellation is that is very... [Pg.402]

In 1817, Josef Fraunhofer (1787-1826) studied the spectrum of solar radiation, observing a continuous spectrum with numerous dark lines. Fraunhofer labeled the most prominent of the dark lines with letters. In 1859, Gustav Kirchhoff (1824-1887) showed that the D line in the solar spectrum was due to the absorption of solar radiation by sodium atoms. The wavelength of the sodium D line is 589 nm. What are the frequency and the wavenumber for this line ... [Pg.371]

The ubiquitous use of the word Tine to describe an experimentally observed transition goes back to the early days of observations of visible spectra with spectroscopes in which the lines observed in, say, the spectmm of a sodium flame are images, formed at various wavelengths, of the entrance slit. Although, nowadays, observations tend to be in the form of a plot of some measure of the intensity of the transition against wavelength, frequency or wavenumber, we still refer to peaks in such a spectmm as lines. [Pg.34]

Fig. 4. Physical property curves for aqueous sodium lauryl sulfate where A is detergency B, density change C, conductivity (high frequency) D, surface... Fig. 4. Physical property curves for aqueous sodium lauryl sulfate where A is detergency B, density change C, conductivity (high frequency) D, surface...
Superchlorination typically refers to a dding FAC equal to 10 x ppm CAC, whereas shock treatment generally involves addition of 10 ppm FAC. The frequency of superchlorination or shock treatment depends on bather load and temperature. Calcium hypochlorite, because of its convenience, is widely used for superchlorination and shock treatment. Sodium hypochlorite, LiOCl, or chlorine gas are also used. Chloroisocyanurates are not recommended since their use would result in excessive cyanuric acid concentrations. [Pg.298]

Properties. Thienamycin is isolated as a colorless, hygroscopic, zwitterionic soHd, although the majority of carbapenems have been obtained as sodium salts and, in the case of the sulfated olivanic acids, as disodium salts (12). Concentrated aqueous solutions of the carbapenems are generally unstable, particularly at low pH. AH the substituted natural products have characteristic uv absorption properties that are often used in assay procedures. The ir frequency of the P-lactam carbonyl is in the range 1760 1790 cm . ... [Pg.4]

Barium sodium niobium oxide [12323-03-4] Ba2NaNb 02, finds appHcation for its dielectric, pie2oelectric, nonlinear crystal and electro-optic properties (35,36). It has been used in conjunction with lasers for second harmonic generation and frequency doubling. The crystalline material can be grown at high temperature, mp ca 1450°C (37). [Pg.482]

A fairly detailed risk analysis of fires was in the Clinch River Breeder Reactor (CRBR) Risk Assessment Study, 1977. In this study, FMEA was used to identify important fire locations for a wide variety of combustibles, including cables, oil, and sodium. The resulting estimate of the frequency of fire-induced core melt, 5E-7 per reactor-year, is substantially below the estimates discussed above. [Pg.196]

A slight but systematic decrease in the wave number of the complexes bond vibrations, observed when moving from sodium to cesium, corresponds to the increase in the covalency of the inner-sphere bonds. Taking into account that the ionic radii of rubidium and cesium are greater than that of fluorine, it can be assumed that the covalent bond share results not only from the polarization of the complex ion but from that of the outer-sphere cation as well. This mechanism could explain the main differences between fluoride ions and oxides. For instance, melts of alkali metal nitrates display a similar influence of the alkali metal on the vibration frequency, but covalent interactions are affected mostly by the polarization of nitrate ions in the field of the outer-sphere alkali metal cations [359]. [Pg.181]

For a typical sodium atom, the initial velocity in the atomic beam is about 1000 m s1 and the velocity change per photon absorbed is 3 crn-s. This means that the sodium atom must absorb and spontaneously emit over 3 x 104 photons to be stopped. It can be shown that the maximum rate of velocity change for an atom of mass m with a photon of frequency u is equal to hu/lmcr where h and c are Planck s constant and the speed of light, and r is the lifetime for spontaneous emission from the excited state. For sodium, this corresponds to a deceleration of about 106 m s"2. This should be sufficient to stop the motion of 1000 m-s 1 sodium atoms in a time of approximately 1 ms over a distance of 0.5 m, a condition that can be realized in the laboratory. [Pg.187]

Hisatsune and co-workers [290—299] have made extensive kinetic studies of the decomposition of various ions in alkali halide discs. Widths and frequencies of IR absorption bands are an indication of the extent to which a reactant ion forms a solid solution with the matrix halide. Sodium acetate was much less soluble in KBr than in KI but the activation energy for acetate breakdown in the latter matrix was the larger [297]. Shifts in frequency, indicating changes in symmetry, have been reported for oxalate [294] and formate [300] ions dispersed in KBr. [Pg.29]

Sodium dodecyl sulfate has been used to modify polypyrrole film electrodes. Electrodes synthesized in the presence of sodium dodecyl sulfate have improved redox processes which are faster and more reversible than those prepared without this surfactant. The electrochemical behavior of these electrodes was investigated by cyclic voltametry and frequence response analysis. The electrodes used in lithium/organic electrolyte batteries show improved performance [195]. [Pg.275]

Figure 2.3. Catalysis (0), classical promotion ( ), electrochemical promotion ( , ) and electrochemical promotion of a classically promoted (sodium doped) ( , ) Rh catalyst deposited on YSZ during NO reduction by CO in presence of gaseous 02.14 The Figure shows the temperature dependence of the catalytic rates and turnover frequencies of C02 (a) and N2 (b) formation under open-circuit (o.c.) conditions and upon application (via a potentiostat) of catalyst potential values, UWr, of+1 and -IV. Reprinted with permission from Elsevier Science. Figure 2.3. Catalysis (0), classical promotion ( ), electrochemical promotion ( , ) and electrochemical promotion of a classically promoted (sodium doped) ( , ) Rh catalyst deposited on YSZ during NO reduction by CO in presence of gaseous 02.14 The Figure shows the temperature dependence of the catalytic rates and turnover frequencies of C02 (a) and N2 (b) formation under open-circuit (o.c.) conditions and upon application (via a potentiostat) of catalyst potential values, UWr, of+1 and -IV. Reprinted with permission from Elsevier Science.
Figure 8.65. Dependence of the catalytic rates and turnover frequencies of C02 on the reaction temperature and on the catalyst potential for the initially sodium free Rh/YSZ catalyst (labeled C2) during NO reduction by CO in presence of gaseous 02. Reprinted with permission from Elsevier Science. Figure 8.65. Dependence of the catalytic rates and turnover frequencies of C02 on the reaction temperature and on the catalyst potential for the initially sodium free Rh/YSZ catalyst (labeled C2) during NO reduction by CO in presence of gaseous 02. Reprinted with permission from Elsevier Science.
Fig. 1. EPR spectrum of the dithionite-reduced Fepr protein fromD. vulgaris [from (7)]. The protein was 272 ftmol dm" in 25 mmol dm Hepes buffer, pH 7.5, and was reduced under argon with 10 mmol dm sodium dithionite for 3 min at ambient temperature. EPR conditions microwave frequency, 9331 3 MHz modulation frequency, 100 kHz modulation amplitude, 0.63 mT microwave power, 200 mW temperature (relative gain) 16 K (6.3X). Fig. 1. EPR spectrum of the dithionite-reduced Fepr protein fromD. vulgaris [from (7)]. The protein was 272 ftmol dm" in 25 mmol dm Hepes buffer, pH 7.5, and was reduced under argon with 10 mmol dm sodium dithionite for 3 min at ambient temperature. EPR conditions microwave frequency, 9331 3 MHz modulation frequency, 100 kHz modulation amplitude, 0.63 mT microwave power, 200 mW temperature (relative gain) 16 K (6.3X).
PhNH2 reacts with ethylene in the presence of alkali metals, e.g., sodium deposited on alumina, to afford the hydroamination product in good yield but with a low turnover frequency (TOP = mol of product synthesized per mol of catalyst in 1 h) (Bq. 4.3) [44]. [Pg.94]


See other pages where Sodium frequencies is mentioned: [Pg.35]    [Pg.371]    [Pg.204]    [Pg.435]    [Pg.241]    [Pg.383]    [Pg.437]    [Pg.345]    [Pg.443]    [Pg.293]    [Pg.332]    [Pg.84]    [Pg.596]    [Pg.1176]    [Pg.1300]    [Pg.1302]    [Pg.1307]    [Pg.1309]    [Pg.1319]    [Pg.7]    [Pg.528]    [Pg.186]    [Pg.146]    [Pg.652]    [Pg.676]    [Pg.210]    [Pg.231]    [Pg.232]    [Pg.121]    [Pg.140]    [Pg.304]    [Pg.150]    [Pg.332]    [Pg.37]   
See also in sourсe #XX -- [ Pg.290 ]




SEARCH



© 2024 chempedia.info