Hydrophobic adsorption, incompatibility

Interface and colloid science has a very wide scope and depends on many branches of the physical sciences, including thermodynamics, kinetics, electrolyte and electrochemistry, and solid state chemistry. Throughout, this book explores one fundamental mechanism, the interaction of solutes with solid surfaces (adsorption and desorption). This interaction is characterized in terms of the chemical and physical properties of water, the solute, and the sorbent. Two basic processes in the reaction of solutes with natural surfaces are 1) the formation of coordinative bonds (surface complexation), and 2) hydrophobic adsorption, driven by the incompatibility of the nonpolar compounds with water (and not by the attraction of the compounds to the particulate surface). Both processes need to be understood to explain many processes in natural systems and to derive rate laws for geochemical processes. 

Balazs and Lewandowski (1990) have performed simulations of the adsorption of triblock copolymers onto a planar surface, and examined the conformations of the adsorbed chains. Monte Carlo simulations were performed of the motion of hydrophilic-hydrophobic chains on a cubic lattice. These simulations revealed a complex structure in the interfacial region due to the self-assembly of chains, driven by the solvent-incompatible block, reducing adsorption onto the surface. The influence on the surface coverage of length of the hydrophilic segement, polymer concentration, interaction energy between hydrophilic block and the... 

It is known that, in a polymer blend, thermodynamic incompatibility between polymers usually causes demixing of polymers. If the polymer is equilibrated in air, the polymer with the lowest surface energy (hydrophobic polymer) will concentrate at the air interface and reduce the system s interfacial tension as a consequence. The preferential adsorption of a polymer of lower surface tension at the surface was confirmed by a number of researchers for a miscible blend of two different polymers. Based on this concept, surface modifying macromolecules (SMMs) as surface-active additives were synthesized and blended into polymer solutions of polyethersulfone (PES). Depending on the hydro-phobic or hydrophilic nature of the SMM, the membrane surface becomes either more hydrophobic or more hydrophilic than the base polymeric material. ... 

Fluorocarbon and hydrocarbon surfactants present a maximum of incompatibility near the equimolar composition of the mixture at which the electrostatic repulsion is enhanced by the lipophobic character of the fluorocarbon hydrophobic group. Since the I, potential in the equimolecular case is almost half the value attained with the pure surfactants, it may be conjectured that the adsorption density is considerably reduced by the extra repulsion provided by the lipophobic effect of the fluorocarbon group. 

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