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Ionization, rate

The relatively low pX values seen for the benzoyl acetanilides, especiaHy as two-equivalent couplers, minimize concerns over slow ionization rates and contribute to the couplers overaH reactivity. But this same property often results in slow reprotonation in the acidic bleach, where developer carried over from the previous step can be oxidized and react with the stiH ionized coupler to produce unwanted dye in a nonimage related fashion. This problem can be eliminated by an acidic stop bath between the developer and the bleach steps or minimized by careful choice of coupling-off group, coupler solvent, or dispersion additives. [Pg.476]

Steric and Strain Effects on Substitution and Ionization Rates... [Pg.298]

SECTION 5.7 STERIC AND STRAIN EFFECTS ON SUBSTITUTION AND IONIZATION RATES... [Pg.299]

Throughout this section attention is restricted to rate equations that include concentrations of only the substrate, H, and OH. The observed first-order rate constant, therefore, contains concentrations of only H and OH (the quantity [OH ] is often replaced by A",v/[H j). The substrate (reactant) may be ionizable. Rate equations containing the concentration of additional solutes (especially catalytic additives) can be developed as shown in Section 6.3. [Pg.274]

The simulated rate of vibrational excitation at 30 MHz is already twice that at 13.56 MHz. At 65 MHz, this rate is three times the rate at 13.56 MHz. The dissociation and ionization rates do not change much. The increase of the vibrational excitation leads to an increase of the density of excited SiH4 molecules. This agrees with an N2 discharge experiment where the vibrational temperature of N2 was observed to rise with the applied frequency [282]. [Pg.78]

It is worth noting that the ionization rate increases significantly if the Al content of the zeolite framework increases. [Pg.380]

The source of some of the difficulties encountered in trying to explain the effects of structural changes on ionization rates may be due to the different parts played by the solvent, as for example, the sulfur dioxide of the trityl chloride equilibrium experiments and the aqueous acetone of the benzhydryl chloride rate data. The solvent is bound to modify the effect of a substituent, and although the solvent is usually ignored in discussing substituent effects this is because of a scarcity of usable data and not because the importance of the solvent is not realized "... solvation energy and entropy are the most characteristic determinants of reactions in solution, and... for this class of reactions no norm exists which does not take primary account of solvation. 220 Precisely how best to take account of solvation is an unanswered problem that is the subject of much current research. [Pg.112]

Fig. 2. A plot of log ionization rate constant against log acid dissociation constant for some carbon acids in water at 25°, 346... Fig. 2. A plot of log ionization rate constant against log acid dissociation constant for some carbon acids in water at 25°, 346...
While excitation processes in strong laser fields have not received as much attention as ionization rates and high-harmonic generation, the study of excitation is an important aspect of our overall understanding of the behavior of molecules in strong laser fields. [Pg.17]

In the case of vibrational motion in the ground electronic state produced by LF, the study of the vibrational motion can provide information about how the ionization rate of the state depends on R. For I2, certain theoretical calculations predicted that the ionization rate would decrease as R increased, at least near Req [28]. However, the experimental results showed the opposite trend. [Pg.17]

The example of I2 actually has a bigger problem. In quantum tomography, the angular dependence to the ionization rate must be taken into account for... [Pg.17]

Considering that J 2 I 2 and that the ionization rates at R = Rq have little 9 dependence [35], the dominant difference should be due to the electron and nuclear dynamics in the steps 2 and 3. The observed single molecule responses are obtained by superposing the radiation from all the molecules with random orientation coherently. For linearly polarized laser field, whose direction is defined as x axis, the observed dipole moment is given by... [Pg.78]

In practice the differing ionization rates for the individual gases will be taken into account by standardization against nitrogen relative ionization probabilities (RIP) in relationship to nitrogen will be indicated (Table 4.3). [Pg.103]


See other pages where Ionization, rate is mentioned: [Pg.2062]    [Pg.2479]    [Pg.116]    [Pg.186]    [Pg.124]    [Pg.128]    [Pg.135]    [Pg.110]    [Pg.111]    [Pg.112]    [Pg.148]    [Pg.57]    [Pg.69]    [Pg.69]    [Pg.139]    [Pg.365]    [Pg.19]    [Pg.255]    [Pg.257]    [Pg.332]    [Pg.339]    [Pg.78]    [Pg.92]    [Pg.114]    [Pg.1]    [Pg.5]    [Pg.15]    [Pg.98]    [Pg.141]    [Pg.391]    [Pg.255]   
See also in sourсe #XX -- [ Pg.53 , Pg.167 , Pg.170 , Pg.173 , Pg.176 , Pg.177 , Pg.180 , Pg.203 ]

See also in sourсe #XX -- [ Pg.287 , Pg.307 ]




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Atmospheric pressure chemical ionization flow rate through

Atmospheric-pressure-chemical-ionization flow rates

Avalanche ionization rate

Cosmic ray ionization rate

Electric fields ionization rates

Electron Ionization and Fragmentation Rates

Electrospray ionization flow rate limitations

Field ionization rates

Geometrical Influences on Rate of Ionization

Ionization rate constant

Ionization variables flow rate

Rate constant of ionization

Rate of ionization

Rate state-specific ionization

Rates of Chemi-ionization

Solvent Effects on Rate of Ionization

State-specific ionization rate constant

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