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Proton concentration and

The activities a, of dilute solutions are simply the concentrations of the solutes and the equilibrium constant can be used to determine the pH of a solution when a known amount of acid is dissolved in water. The proton concentration and hence pH is given by the solution of the general quadratic ... [Pg.235]

Figure 25. Proton conductivity of various oxides, as calculated from data on proton concentrations and mobilities, according to Norby and Larring (the type of dopant is not indicated see ref 187 for source data). The conductivity of oxides with a perovskite-type structure are shown by bold lines, and the conductivity of the oxide ion conductor YSZ (yttria-stabilized zirconia) is shown for comparison, (reproduced with the kind permission of Annual Reviews, http //www.AnnualReviews.org). Figure 25. Proton conductivity of various oxides, as calculated from data on proton concentrations and mobilities, according to Norby and Larring (the type of dopant is not indicated see ref 187 for source data). The conductivity of oxides with a perovskite-type structure are shown by bold lines, and the conductivity of the oxide ion conductor YSZ (yttria-stabilized zirconia) is shown for comparison, (reproduced with the kind permission of Annual Reviews, http //www.AnnualReviews.org).
The lactate and proton concentrations, and hence the pH in the blood, depend not only on the rate of release from muscle, and other tissues, but also on the rate of their removal from the blood. The transporter that transports lactate and protons out of cells also transports them into cells. There are two tissues that are important in then-removal from the blood liver and heart (Figure 6.8). [Pg.102]

Fig. 19-17), the electrochemi- 192°-1992 cal energy inherent in the difference in proton concentration and separation of charge across the inner mitochondrial membrane—the proton-motive force—drives the synthesis of ATP as protons flow passively back into the matrix through a proton pore associated with ATP synthase. To emphasize this crucial role of the proton-motive force, the equation for ATP synthesis is sometimes written... [Pg.704]

A prediction of the chemiosmotic theory is that, because the role of electron transfer in mitochondrial ATP synthesis is simply to pump protons to create the electrochemical potential of the proton-motive force, an artificially created proton gradient should be able to replace electron transfer in driving ATP synthesis. This has been experimentally confirmed (Fig. 19-20). Mitochondria manipulated so as to impose a difference of proton concentration and a separation of charge across the inner membrane synthesize ATP in the absence of an oxidizable substrate the proton-motive force alone suffices to drive ATP synthesis. [Pg.707]

CH is the hydrogen concentration in the solid, which is equivalent to the proton concentration and h2 are the pressures of hydrogen in the gas phase... [Pg.234]

If to a mixture of a weak acid and its conjugate base one adds protons (e.g., HC1), the conjugate base (the acetate ion) will combine with the protons to form undissociated acetic acid to maintain the Kd at the appropriate level [Equation (3.5)]. The proton concentration and the pH will remain relatively stable. Likewise, if to the mixture of a weak acid and its conjugate base one added OH- ions (e.g., NaOH), the OH" will combine with the protons present to form the inert H20. To maintain the Kd [Equation (3.5)], acetic acid will dissociate to replenish the protons removed, again resulting in reestablishment of nearly the original pH. [Pg.32]

The retention volume of the analyte as a function of the proton concentration and concentration of counteranions is shown below ... [Pg.66]

Here A 1 2 is the coupling constant, which ties protons in the polar low-frequency mode (coj = 99 cm ) n is the proton concentration, and g the lattice constant. [Pg.432]

Figure 31 The generation of final products H+ and Cl during the photodegradation of 0.028 mmol/L DR in Tween 80 surfactant solutions at 253.7 nm. The HPLC analysis and UWVisible spectrometric analysis (color) of the DR is also compared. Photodecolouration occurred with a time delay after the photodechlorination. Generation of proton concentration and chloride concentration is 1 1 stoichiometricly matched. Figure 31 The generation of final products H+ and Cl during the photodegradation of 0.028 mmol/L DR in Tween 80 surfactant solutions at 253.7 nm. The HPLC analysis and UWVisible spectrometric analysis (color) of the DR is also compared. Photodecolouration occurred with a time delay after the photodechlorination. Generation of proton concentration and chloride concentration is 1 1 stoichiometricly matched.
This scheme was confirmed by kinetic measurements showing the dependence of the reaction rate on the proton concentration and ionic strength and also by formation of diphenylcarbinol from bis(diphenyl-methyl)ether (Scheme 86). [Pg.52]

Similar results are derived for other weak acids and for ammonia (Warneck, 1986). In each case one can define a factor /a, which expresses the dependence on proton concentration, and a modified Henry s law coefficient... [Pg.396]

Addition of base or acid had, however, a significant impact on the stability and yield of the characteristic 1080 nm absorption band. A semilogarithmic correlation between the proton concentration and the intensity of the fullerene 7t-radical anion band (1080 nm) is observed in anaerobic aqueous solutions. This observation has been ascribed to a reversible protonation of Ceo /Y-CD. Experimental proof for this assumption was brought forward by the fact that the 1080 nm absorption, in an alkaline solution (pH 10), diminished upon acidifying (pH 3) and was completely restored upon addition of base (pH 10). The reversible protonation process gives rise to a pKa of 4.5. [Pg.263]

This leaves the second order rate coefficient for toluene nitration in aqueous solution (k) as the only missing parameter. The most reliable data are probably those of Coombes et al(25). Unfortunately, they used nitric acid concentrations much below those found in heterogeneous nitrations and there is some uncertainty as to how they should best be extrapolated. Thus Cox and Strachan(9 ) have attributed deviations in their results to the probability of k values in their nitrating mixtures being higher than those measured by Coombes et al. Schiefferle(26) found it necessary to modify the acidity function concept to account for the contribution of the nitric acid dissociation to the proton concentration and suggested that k should be related to the total acidity rather than just the sulphuric acid concentration. A model based on this concept gave a better fit to his experimental results. [Pg.203]


See other pages where Proton concentration and is mentioned: [Pg.320]    [Pg.101]    [Pg.666]    [Pg.827]    [Pg.384]    [Pg.231]    [Pg.295]    [Pg.320]    [Pg.36]    [Pg.82]    [Pg.703]    [Pg.32]    [Pg.236]    [Pg.571]    [Pg.761]    [Pg.55]    [Pg.50]    [Pg.320]    [Pg.418]    [Pg.230]    [Pg.108]    [Pg.172]    [Pg.538]    [Pg.82]    [Pg.703]    [Pg.666]    [Pg.410]    [Pg.22]    [Pg.383]    [Pg.589]    [Pg.890]    [Pg.314]    [Pg.620]   
See also in sourсe #XX -- [ Pg.248 ]

See also in sourсe #XX -- [ Pg.248 ]




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Proton concentration

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