Foundations of Colloid Science, Volume 2While Volume I stands as an essentially complete advanced textbook of colloidal science, Volume II extends the material to include important new areas, and develops some of the topics in much greater depth. An introductory chapter on the theory of liquids describes the concept of correlation functions and the use of Fourier transforms to analyse the scattering of light and neutrons by colloidal systems. Absorption is given detailed coverage and a chapter on electrokinetics introduces a new approach to time-dependent processes in the double layer. The principles of double layer theory are also used to review the behavior of thin films and emulsions. A final chapter on the rheology of colloidal suspensions calls on many of the concepts developed earlier to bring some cohesion to this important and rapidly developing field. |
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Page 704
However , by omitting unmanageable terms , one can obtain an approximate
expression for c ( r ) . This procedure generates a class of approximation
schemes with names such as the Hypernetted Chain ( HNC ) , the Percus -
Yevick ( PY ) ...
However , by omitting unmanageable terms , one can obtain an approximate
expression for c ( r ) . This procedure generates a class of approximation
schemes with names such as the Hypernetted Chain ( HNC ) , the Percus -
Yevick ( PY ) ...
Page 858
particles , and is usually not even a rough approximation otherwise . The reason
is that we have used the condition of spherical symmetry in its derivation , and '
slightly broken ' symmetry is usually meaningless . More formally , if we expand ...
particles , and is usually not even a rough approximation otherwise . The reason
is that we have used the condition of spherical symmetry in its derivation , and '
slightly broken ' symmetry is usually meaningless . More formally , if we expand ...
Page 860
These dispersions are precisely those where the decoupling approximation may
be expected to work , but before applying it we must decide how to choose the
mean interaction potential which will be used to calculate s ( Q ) for the
equivalent ...
These dispersions are precisely those where the decoupling approximation may
be expected to work , but before applying it we must decide how to choose the
mean interaction potential which will be used to calculate s ( Q ) for the
equivalent ...
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Contents
Contents of Volume I | 675 |
ADSORPTION FROM SOLUTION | 709 |
THE ELECTROKINETIC EFFECTS 786 13 THE ELECTROKINETIC EFFECTS | 786 |
Copyright | |
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adsorbed adsorption applied approach approximation assumed average becomes behaviour bulk calculated Chapter charge Chem Colloid interface Sci colloidal component concentration constant correlation corresponding density depends described determined developed direction discussed dispersion distance double layer droplets effect electrical electrokinetic electrolyte emulsion energy equation equilibrium estimate et al example Exercise experimental expression factor field film flow fluid force fraction function given gives groups important increases interaction interface involved ions limit liquid material measured microemulsion molecules Note observed obtained occur pair parameters particles phase positive possible potential present pressure problem procedure radius range reduces referred region result scattering Section separation shear rate shown solution specific spheres stability stress structure surface surface charge surface tension suspension theory thin usually values viscosity volume zero