Big Chemical Encyclopedia

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

Articles Figures Tables About

Atoms, energy dissociation

McFeely and co-workers used soft x-ray photoelectron spectroscopy (SXPS) to measure the changes in binding energies of Si(2p) levels after slight exposure to fluorine atoms via dissociative chemisoriDtion of XeF2 [39]. Using synclirotron radiation at 130 eV as the source enabled extreme surface sensitivity. Since this level is split into a... [Pg.2932]

All heteronuclear diatomic molecules, in their ground electronic state, dissociate into neutral atoms, however strongly polar they may be. The simple explanation for this is that dissociation into a positive and a negative ion is much less likely because of the attractive force between the ions even at a relatively large separation. The highly polar Nal molecule is no exception. The lowest energy dissociation process is... [Pg.389]

Amplitude of a process, 114. Andrew s diagram, 173 Anisotropic bodies, 193 Aphorism of Clausius, 83, 92 Arrhenius theory of electrolytic dissociation, 301 Aschistic process, 31, 36, 51 Atmosphere, 39 Atomic energy, 26 Availability, 65, 66 Available energy, 66, 77, 80, 98, 101... [Pg.539]

In all the other sehemes (UHF, PHF, EHF), the dissociation limit is the correct one corresponding to two neutral hydrogen atoms (2H-) each FSGO-hydrogen atom energy is thus obtained by the simple variational procedure ... [Pg.196]

In practice, the harmonic oscillator has limits. In the ideal case, the two atoms can approach and recede with no change in the attractive force and without any repulsive force between electron clouds. In reality, the two atoms will dissociate when far enough apart, and will be repulsed by van der Waal s forces as they come closer. The net effect is the varying attraction between the two in the bond. When using a quantum model, the energy levels would be evenly spaced, making the overtones forbidden. [Pg.167]

Obtained from experimental dissociation energies and estimated total atomic energies, see text. c lAi state. [Pg.19]

Atomization Energy. The energy of dissociation of an atom or molecule into separated nuclei and electrons. Atomization energy is the quantity which is calculated in G2 and G3 Models. [Pg.754]

We assume that we have a solid metal M which reacts with a diatomic, gaseous nonmetal X2 (e.g., CI2, F2, 02). Similar cycles can be written for solid elements such as sulfur as the nonmetal. In either case, before we can connect U with AHf we must form gaseous ions of M and X. We need not only the relevant ionization potentials (IP) and electron affinities (EA), but also the heats of atomization of solid M and gaseous X2. These atomization energies are traditionally referred to as heats of sublimation AHsuh of M(s) and of dissociation AHd ss of X2. For NaCl itself, we have... [Pg.90]

For addition of Cl atoms, the dissociation energy of the radicals AX has been estimated at about 20-22 kcal./mole. At room temperature k ifki(A) should be well below 10-3 and mechanism (C) should be obeyed and has indeed been frequently observed. At higher temperatures (about 225°C.) k 2/k2(A) 10-3 and a change to mechanism (B) should occur. This has been confirmed experimentally by Adam et al. (1) in a study of the photochlorination of tetrachlorethylene. They observed a maximum in the rate and a change in mechanism at about 180°C., as a result of the increased importance of the radical decomposition reaction (—2). From their data they were able to deduce the Arrhenius parameters for this reaction. In extensions of this work Goldfinger and his collaborators have carried out competitive experiments with a number of hydrocarbons and chlorinated hydrocarbons. [Pg.167]

Step 2. The dissociation of gaseous Cl2 molecules into individual Cl atoms. Energy must be added to break molecules apart before reaction can occur, and the energy required for bond breaking therefore has a positive value 243 kj/mol for Cl2 (or 122 kj/mol for 1/2 Cl2). We ll look further into the energetics of bond dissociation in Section 8.11. [Pg.212]


See other pages where Atoms, energy dissociation is mentioned: [Pg.95]    [Pg.359]    [Pg.67]    [Pg.458]    [Pg.165]    [Pg.286]    [Pg.111]    [Pg.300]    [Pg.178]    [Pg.257]    [Pg.116]    [Pg.318]    [Pg.67]    [Pg.558]    [Pg.20]    [Pg.294]    [Pg.72]    [Pg.141]    [Pg.129]    [Pg.137]    [Pg.129]    [Pg.137]    [Pg.24]    [Pg.23]    [Pg.236]    [Pg.187]    [Pg.95]    [Pg.92]    [Pg.34]    [Pg.157]    [Pg.415]    [Pg.369]    [Pg.77]    [Pg.64]    [Pg.32]    [Pg.43]    [Pg.295]    [Pg.1364]    [Pg.1365]   
See also in sourсe #XX -- [ Pg.16 ]




SEARCH



Bond Dissociation Energy. Atomization Enthalpy

Hydrogen atom transfer bond dissociation energies

© 2024 chempedia.info