Foundations of Colloid Science, Volume 1Liquid suspension systems are the basic ingredients of paints, detergents, biological cells, and countless other systems of scientific and technological importance. This book presents the fundamental physical and chemical concepts necessary to the understanding of these systems and of colloid science in general. New ideas are introduced carefully and formulae are developed in full, with exercises to help the reader throughout. The frequent references to the many applications of colloid science will be especially helpful to beginning research scientists and people in industry, medicine and agriculture who often find their training in this area inadequate. Integrating developments from the time of colloid science's infancy forty years ago to its present state as a rigorous discipline, this intelligently assembled work elucidates a remarkable range of concepts, techniques, and behaviors. |
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Page 184
... interaction energy VA , as calculated by the Hamaker summation method of the previous section , is of limited use in colloidal problems where the macrobodies ( particles ) are surrounded not by a vacuum , as assumed in eqn ( 4.4.2 ) ...
... interaction energy VA , as calculated by the Hamaker summation method of the previous section , is of limited use in colloidal problems where the macrobodies ( particles ) are surrounded not by a vacuum , as assumed in eqn ( 4.4.2 ) ...
Page 395
... interaction 7.2 Free energy of formation of a double layer 7.3 Overlap of two flat double layers 7.3.1 Approximate relations for overlap of flat double layers 7.4 Interaction between dissimilar flat plates 7.5 Interaction between two ...
... interaction 7.2 Free energy of formation of a double layer 7.3 Overlap of two flat double layers 7.3.1 Approximate relations for overlap of flat double layers 7.4 Interaction between dissimilar flat plates 7.5 Interaction between two ...
Page 627
... interaction of the molecular charge distributions to obtain the interaction energy operator Vint in the total Hamiltonian for the system . We write : B - Vine = 1 ΣΣ Απερ i TR + F - A ( A1.6 ) where R is the position of the centre of ...
... interaction of the molecular charge distributions to obtain the interaction energy operator Vint in the total Hamiltonian for the system . We write : B - Vine = 1 ΣΣ Απερ i TR + F - A ( A1.6 ) where R is the position of the centre of ...
Contents
CHARACTERIZATION OF COLLOIDAL | 2 |
BEHAVIOUR OF COLLOIDAL DISPERSIONS | 49 |
PARTICLE SIZE AND SHAPE | 104 |
Copyright | |
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adsorbed adsorption aggregation approximation aqueous assumed behaviour Brownian motion bulk calculated capillary chemical chemical potential coagulation coefficient Colloid interface Sci colloid science colloidal dispersions colloidal particles component constant contact angle crystal curvature curve density determined dielectric diffuse dipole distance distribution DLVO theory double layer droplet effect electrolyte electron electrostatic enthalpic entropy equation equilibrium Establish eqn Exercise experimental flocculation flow fluid force formula free energy frequency function given head group hydrocarbon interaction energy ions liquid material measured method micelle microscope molar mass molecular molecules monomer negative Note obtained occurs Overbeek phase plates polymer potential energy procedure quantity R₁ radius region repulsion result scattering sedimentation separation shear silver iodide solid solution solvent spheres spherical stabilizing moieties steric stabilization stress surface tension surfactant suspension temperature term theory thermodynamic vector velocity viscosity volume Waals x₁ Young-Laplace equation zero