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Elementary reaction

About: Elementary reaction is a research topic. Over the lifetime, 2972 publications have been published within this topic receiving 76110 citations.


Papers
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Journal ArticleDOI
TL;DR: In this paper, the partial oxidation of CH 4 over Rh/Al 2 O 3 was studied by means of temporal analysis of products (TAP), where CH 4 adsorb dissociatively on reduced metal sites and water adsorbed on the support acts as an oxygen source through the inverse spillover of water or hydroxyl onto the Rh particles.

121 citations

Journal ArticleDOI
TL;DR: In this paper, the authors use density functional theory with an explicit solvent model of the electrochemical interface to calculate activation energy barriers for various proton-electron transfer elementary reactions steps for CO2 reduction on Au, Cu, and Pt surfaces.

121 citations

Journal ArticleDOI
Dietmar A. Plattner1
TL;DR: In this paper, the coupling of electrospray ionization to ion-molecule techniques in the gas phase can yield detailed information about elementary reaction steps of transition-metal compounds with fully intact coordination spheres.

119 citations

Journal ArticleDOI
TL;DR: In this article, the process of bimolecular reaction between A and B is given by Eq. (1), taking into account the diffusion step bringing the two reactions in proximity.
Abstract: Chemical reactions require that at least two molecules or reacting groups come into close proximity so that energy, electrical charge, or chemical groups may be exchanged between them. The process of bimolecular reaction between A and B is given by Eq. (1), taking into account the diffusion step bringing the two reactions in proximity, (AB)

118 citations

Book ChapterDOI
Carl Wagner1
TL;DR: In this paper, the thermodynamic activity of an atomic species on the surface of a catalyst and its determination under steady-state conditions of a catalytic reaction is discussed, and a rational rate law is proposed to represent the empirical rate data in a more logical form than an empirical rate law.
Abstract: Publisher Summary This chapter discusses the thermodynamic activity of an atomic species on the surface of a catalyst and its determination under steady-state conditions of a catalytic reaction. If the rate of an individual step of a catalytic reaction depends on the concentration of adsorbed atoms occurring as intermediates, it is imperative to determine this dependence. The determination of the surface concentration of molecules adsorbed on a catalyst is feasible under favorable conditions. In the case of atomic species, it has been found to be convenient to use the thermodynamic activity rather than the surface concentration as the relevant variable. The primary problem of chemical kinetics is the formulation of an empirical rate law that represents the rate of a reaction as a function of the concentrations or partial pressures of reactants, products, and catalysts present in a gaseous or liquid phase. The knowledge of the mechanism of a reaction may be used to formulate a rational rate law that may represent the empirical rate data in a more logical form than an empirical rate law.

117 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
202321
202229
202185
202088
201971
201871