The rôle of diffusion during catalysis by colloidal metals and similar substances.
Author(s) -
Henry J. S. Sand,
John Henry Poynting
Publication year - 1905
Publication title -
proceedings of the royal society of london
Language(s) - English
Resource type - Journals
eISSN - 2053-9126
pISSN - 0370-1662
DOI - 10.1098/rspl.1904.0127
Subject(s) - diffusion , nernst equation , chemical reaction , catalysis , boundary (topology) , colloid , convection , chemistry , colloidal particle , thermodynamics , chemical equilibrium , chemical physics , physics , organic chemistry , mathematics , mathematical analysis , electrode
In a paper on reaction-velocities in heterogeneous systems, Nernst has recently put forward the view that all chemical reactions taking place on the boundary of two phases proceed to equilibrium practically instantaneously, and that the velocities actually observed are simply those with which diffusion and convection renew the reacting material at the boundary. As a special instance of heterogeneous reactions, he mentions catalytic decompositions due to finely divided particles, such as colloidal metals, and he believes it probable that the kinetics of these reactions can be deduced from the assumption that chemical equilibrium remains permanently established on the surface of the particles.
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