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Relative reduction rates

Relative reduction rates of ferrioxamine, hexacyanoferrate(III) and iron(III) complexes of edta and citrate by ferri-reductase have been established. ... [Pg.513]

Table I. Relative reduction rates (AE365 min-1) of veratraldehyde and the quinones 13-15 by partially purified reductases from P. chrysospo-rivm... Table I. Relative reduction rates (AE365 min-1) of veratraldehyde and the quinones 13-15 by partially purified reductases from P. chrysospo-rivm...
P 14.7 Evaluating Relative Reduction Rates in an Anaerobic Sediment... [Pg.607]

Figure 26.13 (a) Calculated magnitudes of electrochemical reduction rate k at a (9,0) m- and a (10,0) s-SWCNT with a coupling agent having a redox potential of = -0.55 V. (h) Calculated relative reduction rate based on the curves computed in (a). The dash-dotted line... [Pg.582]

Fig. 5.6. Relative reduction rates of oxygen on porous lead electrodes. Fig. 5.6. Relative reduction rates of oxygen on porous lead electrodes.
Figure 5. Relative reduction rates or nitroarenes/heteroarenes at pH 7 are controlled by the substrate reduction potential. Data from [147-149]. Figure 5. Relative reduction rates or nitroarenes/heteroarenes at pH 7 are controlled by the substrate reduction potential. Data from [147-149].
FIGURE 3.9 Relative reduction rates of electron acceptors as a function of time after flooding a soil. [Pg.44]

Figure 6. Relative reduction rates for Fe(III)cytochrome c in presence of 1.2 equiv. of cyclic peptides. Figure 6. Relative reduction rates for Fe(III)cytochrome c in presence of 1.2 equiv. of cyclic peptides.
Figure 7. Relative reduction rates for second generation protein surface receptors. Figure 7. Relative reduction rates for second generation protein surface receptors.
In Figure 9 plots of the logarithms of the relative reduction rates (k ei, relative to 4-Cl) of ten mono-substituted nitrobenzenes versus their values for two different systems illustrate the usefulness of initial rates for inferring information on reaction mechanism(s). [Pg.215]

Figure 14. Comparison of the relative reduction rates (krei, the rates are relative to 4-Cl) of the mono-substituted nitrobenzenes listed in Table 4 in three different systems (a) in aqueous solutions containing hydrogen sulfide and natural organic matter data from (11) (b) in aqueous solutions containing cysteine and a water soluble iron porphyrin data from (64) (c) in aquifer columns under ferrogenic conditions data from (25) The relative rates, expressed as log k gi, are plotted against the normalized one-electron reduction potentials, [El, (ArN02)/0.059 V], of the compounds. Figure 14. Comparison of the relative reduction rates (krei, the rates are relative to 4-Cl) of the mono-substituted nitrobenzenes listed in Table 4 in three different systems (a) in aqueous solutions containing hydrogen sulfide and natural organic matter data from (11) (b) in aqueous solutions containing cysteine and a water soluble iron porphyrin data from (64) (c) in aquifer columns under ferrogenic conditions data from (25) The relative rates, expressed as log k gi, are plotted against the normalized one-electron reduction potentials, [El, (ArN02)/0.059 V], of the compounds.

See other pages where Relative reduction rates is mentioned: [Pg.596]    [Pg.36]    [Pg.156]    [Pg.493]    [Pg.862]    [Pg.43]    [Pg.43]   
See also in sourсe #XX -- [ Pg.462 , Pg.464 ]




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