Because the double layer force vanishes in the absence of surface charges, one expects the attractive van der Waals force to cause the coagulation of all neutral (or even weekly
charged) colloids. The absence of such a behavior has been explained by the existence of an additional (non-DLVO) force, the hydration interaction, which is due to the structuring
of water in the vicinity of hydrophilic surfaces. This chapter is devoted to the identification of the microscopic origin of the hydration force, and to the presentation of a unified treatment of the double layer and hydration forces, the Polarization Model.
Decay Length Polarization Model DLVO Theory Surface Dipole Chemical Free Energy
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.
This is a preview of subscription content, log in to check access.