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Surface chemistry kinetics

Surface chemistry Kinetics of heterogeneous chemical reactions... [Pg.436]

Creighton J R and Bansenauer B A 1993 The surface chemistry and kinetics of GaAs atomic iayer epitaxy Thin Solid Films 225 17-25... [Pg.2944]

Various plasma diagnostic techniques have been used to study the SiH discharges and results have helped in the understanding of the growth kinetics. These processes can be categorized as r-f discharge electron kinetics, plasma chemistry including transport, and surface deposition kinetics. [Pg.358]

White, A. F. (1983). Surface chemistry and dissolution kinetics of glassy rocks at 25 . Geochim. Cosmochim. Acta 47,805-815. [Pg.229]

Models of chemical reactions of trace pollutants in groundwater must be based on experimental analysis of the kinetics of possible pollutant interactions with earth materials, much the same as smog chamber studies considered atmospheric photochemistry. Fundamental research could determine the surface chemistry of soil components and processes such as adsorption and desorption, pore diffusion, and biodegradation of contaminants. Hydrodynamic pollutant transport models should be upgraded to take into account chemical reactions at surfaces. [Pg.140]

Finally, although both temperature-programmed desorption and reaction are indispensable techniques in catalysis and surface chemistry, they do have limitations. First, TPD experiments are not performed at equilibrium, since the temperature increases constantly. Secondly, the kinetic parameters change during TPD, due to changes in both temperature and coverage. Thirdly, temperature-dependent surface processes such as diffusion or surface reconstruction may accompany desorption and exert an influence. Hence, the technique should be used judiciously and the derived kinetic data should be treated with care ... [Pg.279]

Vibrational spectroscopic studies of heterogeneously catalyzed reactions refer to experiments with low area metals in ultra high vacuum (UHV) as well as experiments with high area, supported metal oxides over wide ranges of pressure, temperature and composition [1]. There is clearly a need for this experimental diversity. UHV studies lead to a better understanding of the fundamental structure and chemistry of the surface-adsorbate system. Supported metals and metal oxides are utilized in a variety of reactions. Their study leads to a better understanding of the chemistry, kinetics and mechanisms in the reaction. Unfortunately, the most widely used technique for determining adsorbate molecular structure in UHV,... [Pg.435]

Matthew Hyman and Will Medlin (University of Colorado) review the surface chemistry of electrode reactions, with the intent of introducing this subject to the non-electrochemists. They show the basics of both thermodynamic and kinetic analysis of these reactions, with examples that demonstrate these key principles. [Pg.10]

The aim of this review is to first provide an introduction of electrocatalysis with the hope that it may introduce the subject to non-electrochemists. The emphasis is therefore on the surface chemistry of electrode reactions and the physics of the electrode electrolyte interface. A brief background of the interface and the thermodynamic basis of electrode potential is presented first in Section 2, followed by an introduction to electrode kinetics in Section 3. This introductory material is by no means comprehensive, but will hopefully provide sufficient background for the rest of the review. For more comprehensive accounts, please see texts listed in the references.1-3... [Pg.307]

It has often been argued that clay minerals cannot be used as models for soils in surface chemistry because soil clays are too heterogeneous and impure. The work reported here shows that, for both equilibrium and kinetic studies, standard aluminosilicates are useful models for soils. [Pg.340]

In general, the electrochemical performance of carbon materials is basically determined by the electronic properties, and given its interfacial character, by the surface structure and surface chemistry (i.e. surface terminal functional groups or adsorption processes) [1,2]. Such features will affect the electrode kinetics, potential limits, background currents and the interaction with molecules in solution [2]. From the point of view of electroanalysis, the remarkable benefits of CNT-modified electrodes have been widely praised, including low detection limits, increased sensitivity, decreased overpotentials and resistance to surface fouling [5, 9, 11, 17]. [Pg.123]

Liang, L. (1988) Effects of surface chemistry on the kinetics of coagulation of submicron iron oxide particles (a-Fe203) in water. Ph.D. Thesis Caltech. USA... [Pg.600]

The use of a monolithic stirred reactor for carrying out enzyme-catalyzed reactions is presented. Enzyme-loaded monoliths were employed as stirrer blades. The ceramic monoliths were functionalized with conventional carrier materials carbon, chitosan, and polyethylenimine (PEI). The different nature of the carriers with respect to porosity and surface chemistry allows tuning of the support for different enzymes and for use under specific conditions. The model reactions performed in this study demonstrate the benefits of tuning the carrier material to both enzyme and reaction conditions. This is a must to successfully intensify biocatalytic processes. The results show that the monolithic stirrer reactor can be effectively employed in both mass transfer limited and kinetically limited regimes. [Pg.39]

We continue our study of chemical kinetics with a presentation of reaction mechanisms. As time permits, we complete this section of the course with a presentation of one or more of the topics Lindemann theory, free radical chain mechanism, enzyme kinetics, or surface chemistry. The study of chemical kinetics is unlike both thermodynamics and quantum mechanics in that the overarching goal is not to produce a formal mathematical structure. Instead, techniques are developed to help design, analyze, and interpret experiments and then to connect experimental results to the proposed mechanism. We devote the balance of the semester to a traditional treatment of classical thermodynamics. In Appendix 2 the reader will find a general outline of the course in place of further detailed descriptions. [Pg.286]

Lindemann mechanism, Free radical chain mechanism, Enzyme kinetics, Surface chemistry... [Pg.297]


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See also in sourсe #XX -- [ Pg.492 , Pg.495 ]




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Surface chemistry Kinetics of heterogeneous chemical reaction

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