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Kinetic assessment

The assessment of reaction kinetics by means of batch tests may be strongly affected by dye adsorption on the biophase and supports. The relevance of the adsorption phenomena of dyes on biophase has been addressed in studies regarding free cells [41], granular support biofilm [24], entrapped cells [11, 18], anaerobic sludge [10,24,31,34] and biological activated carbon (BAC) [42,45,47,48]. They have pointed out that the kinetics may be overestimated if the assessment of the adsorption contribution to the dye removal is not taken into account. Under batch conditions, the dye is fastly split between the liquid phase and the biophase, resulting in a sharp reduction of the dye concentration in the liquid phase until adsorption equilibrium is approached. The rate of dye adsorption must be estimated and ruled out in the kinetic assessment. [Pg.113]

Whatever the typology of immobilized biophase, kinetics assessment and modeling studies should not neglect the relevance of the profiles reported in Fig. 4. In agreement with Bailey and Ollis [51], the non uniform profile of the concentrations of azo-dye and of the products may be expressed in terms of the effectiveness factor of the immobilized biophase the ratio of actual reaction rate to the reaction rate without diffusion limitation. [Pg.119]

In accordance with the above, of special interest is kinetic assessment of H202 dissociation to H02 and OH free radicals. Dissociation of H202 in the gas phase is a comprehensively studied reaction proceeding by the mechanism (4.1), from which the following equation is deduced ... [Pg.148]

Khan, M. N Aqueous degradation of N-(hy-droxymethyDphthalimide in the presence of specific and general bases. Kinetic assessment of N-hydroxymethyl derivatives of nitrogen heterocyclics as possible prodrugs, J. Phann. Biomed. Anal.. 7,685, 1989. [Pg.219]

Wei JM, Iglesia E (2004) Isotopic and kinetic assessment of the mechanism of reactions of CH with CO or H O to form synthesis gas and carbon on nickel catalysts. J Catal 224 370... [Pg.291]

Wei, J. and Iglesia, E. Isotopic and kinetic assessment of the mechanism of methane reforming and decomposition reactions on supported iridium catalysts. Physical Chemistry Chemical Physics, 2004, 6, 3754. [Pg.115]

If a rapid screening test is used to assay for the drug or residue that is known to be present in the animal, they key performance element is the specificity of the assay response for the test analyte. A typical use of a rapid screening test in this mode would be in a pharmacokinetic study to determine the half-life of a drug in the blood of a treated animal. The assay used should be able to track the concentration of drug with acceptable specificity and provide a kinetic assessment that reflects the effects of only the animal drug under test. [Pg.29]

Fig. 14. Kinetics of absorbance changes monitored at 832 nm for the re-reduction of P700 in (A) intact PS-I complex [AB] and (B) in HgClj-treated PS-I complex [A-(B>]. (C) and (D) are, respectively, the AA due to the re-reduction of P700 measured at 811 nm and for the AA due to the FeS-X FeS-X reaction measured at 415 nm. See text for details. Figure source Shinkarev, Vassiliev and Golbeck (2000) A kinetic assessment of the sequence ofeiectmn transfer from Fx to Fa ond further to Fb in photosystem I The vaiue of the equiiibrium constant between Fx and Fa- Biophys J 78 365, 366. Fig. 14. Kinetics of absorbance changes monitored at 832 nm for the re-reduction of P700 in (A) intact PS-I complex [AB] and (B) in HgClj-treated PS-I complex [A-(B>]. (C) and (D) are, respectively, the AA due to the re-reduction of P700 measured at 811 nm and for the AA due to the FeS-X FeS-X reaction measured at 415 nm. See text for details. Figure source Shinkarev, Vassiliev and Golbeck (2000) A kinetic assessment of the sequence ofeiectmn transfer from Fx to Fa ond further to Fb in photosystem I The vaiue of the equiiibrium constant between Fx and Fa- Biophys J 78 365, 366.
VP Shinkarev IRVassiliev and JH Golbeck (2000) A kinetic assessment of the sequence of electron transfer from Fx toFfi, and further to Fg in photosystem I The value of equilibrium constant between Fx andFp,. Biophys J 78 363-372... [Pg.504]

R Hisada and T Yagi (1977) 1-methyl-5-methylphenazinium methyl sulfate. J Biochem 82 1469-1473 IR Vassiliev, Y-S Jung, F Yang and JH Golbeck (1998) PsaC subunit of photosystem I is oriented with iron-sulfur clusterFb as the immediate electron donor to ferredoxin and flavodoxin. Biophys J 74 2029-2035 39. VP Shinkarev, IR Vassiliev and JH Golbeck (2000) A kinetic assessment of the sequence of electron transfer from Fx to F and further to Fb in photosystem I The value of equilibrium constant between Fx and F. Biophys J 78 363-372... [Pg.526]

As a simple model reaction for such immobilizations, we investigated the reaction of NHS-CIO SAMs and n-butyl amine in aqueous medium [138, 139]. The coupling reaction was followed analogously to the hydrolysis discussed above by ex situ GIR-FTIR and CA measurements. The corresponding FTIR spectra, as well as the reaction kinetics assessed by both methods, are shown in Fig. 7. [Pg.182]

Apama, V., Dileep, K. V., Mandal, P. K., Karthe, P., Sadasivan, C., Haridas, M. (2012). Anti-Inflammatory Property of n-Hexadecanoic Acid Stmctural Evidence and Kinetic Assessment. Chem Biol Drug Des, 80(3), 434-439. [Pg.35]

Cesium and iodine atoms which are released from fuel specimens into a high-temperature steam-hydrogen environment are thermodynamically unstable and will be rapidly converted into species that are stable under these conditions. Since the chemical form of iodine in particular will considerably influence its transport and retention behavior within the reactor pressure vessel and the primary system, it is important to know the kinetics of these conversion reactions. A kinetics assessment of the most essential reactions (Cronenberg and Osetek, 1988) has shown that for extremely low concentrations of iodine and cesium in steam (e. g. mole ratio I H2O < 10" ), the predominant form of iodine is HI and that of cesium is CsOH. This is due to the fact that because the concentrations of iodine and cesium are so dilute, the elements are much more likely to collide and react with H2O and H2 than with each other. Low concentrations of iodine and cesium increase the time for thermochemical equilibrium to be established for their reaction products. For mixtures which are so dilute in fission products, the reaction times may approach tens of seconds or longer, so that for high effluent rates the environmental conditions may change (e. g. by transport into the next control volume showing other conditions) before thermochemical equilibrium has been achieved. Under such conditions, certain limitations caused by reaction kinetics may exist. [Pg.512]

Kozuch, S. A refinement of everyday thinking The energetic span model for kinetic assessment of catalytic cycles. Wiley Interdiscip. Rev. Comput. Mol. Sci. 2012,2,795-815. [Pg.120]

Yang, C.K., Yamazaki, Y., Aydin, A., and Haile, S.M. (2014) Thermodynamic and kinetic assessments of strontium-doped lanthanum manganite perovskites for two-step thermochemical water splitting. [Pg.860]

Kozuch S (2012) A refinement of evtayday thinking the energetic span model Jot kinetic assessment of catalytic cycles. WIREs Comput Mol Sci 2 795... [Pg.158]


See other pages where Kinetic assessment is mentioned: [Pg.115]    [Pg.239]    [Pg.36]    [Pg.43]    [Pg.116]    [Pg.462]    [Pg.201]    [Pg.115]    [Pg.55]    [Pg.169]    [Pg.170]    [Pg.190]    [Pg.994]    [Pg.11]    [Pg.338]   
See also in sourсe #XX -- [ Pg.190 ]




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