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Kinetics relaxation methods

A large programme utilizing temperature-jump relaxation methods for the study of tautomerism in aqueous solution has led the Dubois group to determine the kinetic and thermodynamic parameters of the equilibrium (130a) (130b) (78T2259). The tautomeric... [Pg.212]

Flynn and Dickens [142] have translated the relaxation methods of fluid kinetics into terms applicable to solid phase thermogravimetry. The rate-determining variables such as temperature, pressure, gas flow rate, gas composition, radiant energy, electrical and magnetic fields are incremented in discrete steps or oscillated between extreme values and the effect on reaction rate determined. [Pg.21]

Transient measnrements (relaxation measurements) are made before transitory processes have ended, hence the current in the system consists of faradaic and non-faradaic components. Such measurements are made to determine the kinetic parameters of fast electrochemical reactions (by measuring the kinetic currents under conditions when the contribution of concentration polarization still is small) and also to determine the properties of electrode surfaces, in particular the EDL capacitance (by measuring the nonfaradaic current). In 1940, A. N. Frumkin, B. V. Ershler, and P. I. Dolin were the first to use a relaxation method for the study of fast kinetics when they used impedance measurements to study the kinetics of the hydrogen discharge on a platinum electrode. [Pg.199]

The Heterogeneous Case. Hachiya et al. (1984) and Hayes and Leckie (1986) used the pressure-jump relaxation method to study the adsorption kinetics of metal ions to oxide minerals. Their results support in essence the same adsorption mechanism as that given for homogeneous complex formation. [Pg.99]

Adsorption-Desorption Kinetics at the Metal-Oxide-Solution Interface Studied by Relaxation Methods... [Pg.230]

Chemical relaxation methods can be used to determine mechanisms of reactions of ions at the mineral/water interface. In this paper, a review of chemical relaxation studies of adsorption/desorption kinetics of inorganic ions at the metal oxide/aqueous interface is presented. Plausible mechanisms based on the triple layer surface complexation model are discussed. Relaxation kinetic studies of the intercalation/ deintercalation of organic and inorganic ions in layered, cage-structured, and channel-structured minerals are also reviewed. In the intercalation studies, plausible mechanisms based on ion-exchange and adsorption/desorption reactions are presented steric and chemical properties of the solute and interlayered compounds are shown to influence the reaction rates. We also discuss the elementary reaction steps which are important in the stereoselective and reactive properties of interlayered compounds. [Pg.230]

Relaxation Method, (2) Experimental Methods and Materials, (3) Surface Reaction Kinetics, (4) Intercalation Kinetics, and (5) Summary and Conclusions. [Pg.231]

The concept of ordered interactions of substrates with the enzyme and ordered dissociation of the products was advanced by Koshland in 1954. From then through the 1960s the introduction of stopped-flow techniques and relaxation methods allowed rapid reactions to be followed and the identification of transient intermediates, from which much more complex kinetic analyses have emerged (Fersht,1977). [Pg.183]

DR. THOMAS The kinetic parameters of micelles are very well known, having been determined by temperature-jump relaxation methods and various other techniques. There are several kinetic events which can be described. First of all, the fastest event is the exchange of the counter ion (e.g., the sodium counter ion, in sodium lauryl sulfate). These ions exchange... [Pg.342]

Potential-relaxation method, 38 27, 34-37 H adsorption, 38 71,75-76 kinetic theory, 38 37-41... [Pg.182]

The appearance or disappearance of the U.V. absorption of the carbonyl group can in principle be used for kinetic measurements. Bell and Jensen (1961) applied this method to 1,3-dichloroacetone the reaction is too fast in pure water, but proceeded at a convenient rate in 5% water-I-dioxan mixtures, in which there is about 50% hydration at equilibrium. Catalysis by many acids and bases was observed. Much faster reactions can be studied by relaxation methods, and the pressure-jump technique has been applied to the reaction Me0(OH)2.CO2H MeC0.C02H-hH20 by Strehlow (1962). [Pg.20]

Kao and Tsien studied the Ca +-binding kinetics of fura-2 and azo-1 by temperature-jump relaxation methods. In 140 mM KCl at 20°C, the respective association and dissociation rate constants for fura-2 were 6x10 M s and 97 s these kinetic properties were insensitive to hydrogen ion concentration over the pH range from 7.4 to 8.4. Azo-1 was studied in 140 mM KCl At 10°C, azo-... [Pg.107]

In electrode kinetics, however, the charge transfer rate coefficient can be externally varied over many orders of magnitude through the electrode potential and kd can be controlled by means of hydrodynamic electrodes so separation of /eapp and kd can be achieved. Experiments under high mass transport rate at electrodes are the analogous to relaxation methods such as the stop flow method for the study of reactions in solution. [Pg.21]

Reductive methylation 274 Regulation of enzymes and metabolic pathways 308 -315 Relaxation methods 137,138 kinetics 139-155 Relaxation time 138 Renin 486... [Pg.326]

The adsorption and desorption kinetics of surfactants, such as food emulsifiers, can be measured by the stress relaxation method [4]. In this, a "clean" interface, devoid of surfactants, is first formed by rapidly expanding a new drop to the desired size and, then, this size is maintained and the capillary pressure is monitored. Figure 2 shows experimental relaxation data for a dodecane/ aq. Brij 58 surfactant solution interface, at a concentration below the CMC. An initial rapid relaxation process is followed by a slower relaxation prior to achieving the equilibrium IFT. Initially, the IFT is high, - close to the IFT between the pure solvents. Then, the tension decreases because surfactants diffuse to the interface and adsorb, eventually reaching the equilibrium value. The data provide key information about the diffusion and adsorption kinetics of the surfactants, such as emulsifiers or proteins. [Pg.2]

It should be noted that this solution procedure requires the knowledge of elementary rate constants, klt k2, and k3. The elementary rate constants can be measured by the experimental techniques such as pre-steady-state kinetics and relaxation methods (Bailey and Ollis, pp. 111 -113, 1986), which are much more complicated compared to the methods to determine KM and rmax. Furthermore, the initial molar concentration of an enzyme should be known, which is also difficult to measure as explained earlier. However, a numerical solution with the elementary rate constants can provide a more precise picture of what is occurring during the enzyme reaction, as illustrated in the following example problem. [Pg.20]

Malnasi-Csizmadia, A., Pearson, D. S., Kovacs, M., Woolley, R. J., Geeves, M. A., and Bagshaw, C. R. (2001). Kinetic resolution of a conformational transition and the ATP hydrolysis step using relaxation methods with a Dictyostelium myosin ii mutant containing a single tryptophan residue. Biochemistry 40, 12727-12737. [Pg.191]

When Bernie Shizgal arrived at UBC in 1970, his research interests were in applications of kinetic theory to nonequilibrium effects in reactive systems. He subsequently applied kinetic theory methods to the study of electron relaxation in atomic and molecular moderators,46 hot atom chemistry, nucleation,47 rarefied gas dynamics,48 gaseous electronics, and other physical systems. An important area of research has been the kinetic theory description of the high altitude portion of planetary atmospheres, and the escape of atmospheric species.49 An outgrowth of these kinetic theory applications was the development of a spectral method for the solution of differential and integral equations referred to as the quadrature discretization method (QDM), which has been used with considerable success in statistical, quantum, and fluid dynamics.50... [Pg.240]

Kinetics and Mechanisms of Rapid Reactions on Soil Constituents Using Relaxation Methods... [Pg.61]

Another chemical relaxation method that can be used to determine the kinetics of fast reactions on soil constituents is the electric field pulse technique. This technique was developed by Hachiya et al. (1980) to study the kinetics of I03 adsorption and desorption on Ti02 and by Sasaki et al. (1983) to investigate ion-pair formation on the surface of a-FeOOH. Excellent review articles on electric field methods are found in DeMaeyer (1969), Hemmes (1979), and Eyring and Hemmes (1986). [Pg.95]

Ikeda, T., Sasaki, M., Astumian, R. D., and Yasunaga, T. (1981). Kinetics of the hydrolysis of zeolite 4A surface by the pressure-jump relaxation method. Bull. Chem. Soc. Jpn. 54, 1885-1886. [Pg.98]

Yasunaga, T., and Ikeda, T. (1986). Adsorption-desorption kinetics at the metal-oxide-solution interface studied by relaxation methods. ACS Symp. Ser. 323, 230-253. [Pg.98]


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See also in sourсe #XX -- [ Pg.401 ]




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