Electrosteric, van der Waals and elastic interaction of polyelectrolyte hydrogels

Abstract

The electrosteric interaction energy for a charged hydrogel and hard plane, and between two charged hydrogels is derived in the Debye–Hückel approximation. This is combined with a van der Waals potential that explicitly addresses the Hamaker constant for the solvent-mediated hydrogel interactions. Then, in the Derjaguin approximation, DLVO-type interaction potentials are provided for hydrogel and hard/rigid spheres, accounting for elastic deformation that accompanies adhesion. As examples, this furnishes the energy for cohesion of soft polyelectrolyte microspheres, and provides a quantitative interpretation for the adhesion of rigid latex spheres to a soft deformable hydrogel, as reported by Sato et al. (Sato et al. 2017 Sci. Rep. 7 , 1–10 ( doi:10.1038/s41598-017-06257-1 )). The theory demonstrates that weak van der Waals attraction of hydrogels is readily balanced by electrosteric interactions, e.g. making colloidal hydrogel dispersions less stable than their rigid-particulate counterparts.