Big Chemical Encyclopedia

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

Articles Figures Tables About

Subject excitations

I have never understood why it is so often assumed by university lecturers that their students are so highly motivated that the usual rules for retaining the attention of an audience, for making the subject exciting, for introducing the elements of humor and drama, can all be suspended. ... [Pg.28]

The classic account of the sinking of the Titanic. A stunning book, incomparably the best on its subject and one of the most exciting books of this or any year - The New York Times... [Pg.446]

The sample is again subjected to a constant magnetic field but all the nuclei are excited by a very short radio frequency pulse. The frequency e (e.g., 400 MHz for a proton at 9.4 tesla) is applied over a period of several... [Pg.64]

Structure defects decrease conductivity of the studied material, and then the intensity of the induced magnetic field is small and the signal received by the probe Hp is big (Fig.2). Low conductivity of austenite is a defects of the structure in case of residual austenite in the martensite structure, which with regard to the magnesite structure is as 1 5. Eddy currents produced in the studied area are subject to excitation in effect of small conductivity of austenite grains in the structure of the studied material. [Pg.20]

Shapes of the ground- and first tln-ee excited-state wavefiinctions are shown in figure AT 1.1 for a particle in one dimension subject to the potential V = which corresponds to the case where the force acting on the... [Pg.17]

Spectral lines are fiirther broadened by collisions. To a first approximation, collisions can be drought of as just reducing the lifetime of the excited state. For example, collisions of molecules will connnonly change the rotational state. That will reduce the lifetime of a given state. Even if die state is not changed, the collision will cause a phase shift in the light wave being absorbed or emitted and that will have a similar effect. The line shapes of collisionally broadened lines are similar to the natural line shape of equation (B1.1.20) with a lifetime related to the mean time between collisions. The details will depend on the nature of the intemrolecular forces. We will not pursue the subject fiirther here. [Pg.1144]

The release of a photon following thermal excitation is called emission, and that following the absorption of a photon is called photoluminescence. In chemiluminescence and bioluminescence, excitation results from a chemical or biochemical reaction, respectively. Spectroscopic methods based on photoluminescence are the subject of Section lOG, and atomic emission is covered in Section lOH. [Pg.423]

Choice of Atomization and Excitation Source Except for the alkali metals, detection limits when using an ICP are significantly better than those obtained with flame emission (Table 10.14). Plasmas also are subject to fewer spectral and chemical interferences. For these reasons a plasma emission source is usually the better choice. [Pg.437]

When possible, quantitative analyses are best conducted using external standards. Emission intensity, however, is affected significantly by many parameters, including the temperature of the excitation source and the efficiency of atomization. An increase in temperature of 10 K, for example, results in a 4% change in the fraction of Na atoms present in the 3p excited state. The method of internal standards can be used when variations in source parameters are difficult to control. In this case an internal standard is selected that has an emission line close to that of the analyte to compensate for changes in the temperature of the excitation source. In addition, the internal standard should be subject to the same chemical interferences to compensate for changes in atomization efficiency. To accurately compensate for these errors, the analyte and internal standard emission lines must be monitored simultaneously. The method of standard additions also can be used. [Pg.438]

The overall requirement is 1.0—2.0 s for low energy waste compared to typical design standards of 2.0 s for RCRA ha2ardous waste units. The most important, ie, rate limiting steps are droplet evaporation and chemical reaction. The calculated time requirements for these steps are only approximations and subject to error. For example, formation of a skin on the evaporating droplet may inhibit evaporation compared to the theory, whereas secondary atomization may accelerate it. Errors in estimates of the activation energy can significantly alter the chemical reaction rate constant, and the pre-exponential factor from equation 36 is only approximate. Also, interactions with free-radical species may accelerate the rate of chemical reaction over that estimated solely as a result of thermal excitation therefore, measurements of the time requirements are desirable. [Pg.56]

Photochemistry. Vinyl chloride is subject to photodissociation. Photexcitation at 193 nm results in the elimination of HCl molecules and Cl atoms in an approximately 1.1 1 ratio (69). Both vinyUdene ( B2) [2143-69-3] and acetylene have been observed as photolysis products (70), as have H2 molecules (71) and H atoms [12385-13-6] (72). HCl and vinyUdene appear to be formed via a concerted 1,1 elimination from excited vinyl chloride (70). An adiabatic recoil mechanism seems likely for Cl atom elimination (73). As expected from the relative stabiUties of the 1- and 2-chlorovinyl radicals [50663-45-1 and 57095-76-8], H atoms are preferentially produced by detachment from the P carbon (72). Finally, a migration mechanism appears to play a significant role in H2 elimination (71). [Pg.415]

The deep violet color of pentaphenylbismuth and certain other pentaarylbismuth compounds has been the subject of considerable speculation. It has been shown by x-ray diffraction (173) that the bismuth atom in pentaphenylbismuth is square—pyramidal. WeU-formed crystals are dichromic, appearing violet when viewed in one plane but colorless in another plane. The nature of the chromophore has been suggested to be a charge-transfer transition by excitation of the four long equatorial bonds ... [Pg.134]

Indazoles have been subjected to certain theoretical calculations. Kamiya (70BCJ3344) has used the semiempirical Pariser-Parr-Pople method with configuration interaction for calculation of the electronic spectrum, ionization energy, tt-electron distribution and total 7T-energy of indazole (36) and isoindazole (37). The tt-densities and bond orders are collected in Figure 5 the molecular diagrams for the lowest (77,77 ) singlet and (77,77 ) triplet states have also been calculated they show that the isomerization (36) -> (37) is easier in the excited state. [Pg.175]


See other pages where Subject excitations is mentioned: [Pg.45]    [Pg.334]    [Pg.1]    [Pg.334]    [Pg.479]    [Pg.45]    [Pg.334]    [Pg.1]    [Pg.334]    [Pg.479]    [Pg.35]    [Pg.56]    [Pg.272]    [Pg.524]    [Pg.419]    [Pg.256]    [Pg.862]    [Pg.1145]    [Pg.1193]    [Pg.1214]    [Pg.1306]    [Pg.2208]    [Pg.2455]    [Pg.2487]    [Pg.2490]    [Pg.2853]    [Pg.3032]    [Pg.100]    [Pg.102]    [Pg.713]    [Pg.713]    [Pg.143]    [Pg.438]    [Pg.135]    [Pg.36]    [Pg.157]    [Pg.262]    [Pg.300]    [Pg.323]    [Pg.74]    [Pg.129]    [Pg.62]    [Pg.586]   
See also in sourсe #XX -- [ Pg.97 ]




SEARCH



Building Subjected to Nonstationary Ground Excitation

Excitation transfer 608 Subject

© 2024 chempedia.info