ABSTRACT:Predictions of the influence of the solvent quality (), the segment-substrate interaction parameter (ps), the chain length (N), and the end cap-substrate interaction parameter (⌬) on the equilibrium-adsorbed amount from a dilute solution of end-functionalized homopolymers (⌫) onto a solid substrate, when both the end cap and polymer segments compete for sites on the surface, were made through application of the self-consistent-field (SCF) theory. These predictions were tested and evaluated through measurement of the equilibrium-adsorbed amount, from a dilute solution of single-end-functionalized custom synthesized relatively monodisperse polystyrenes, possessing an end group (X) chosen to interact with a mildly acidic inorganic substrate (Aerosil 130) and a mildly basic inorganic substrate (aluminum oxide C) through dipole-dipole interactions, hydrogen-bonding interactions, and specific acid-base interactions, as a function of , ps, ⌬, and N. A protocol was developed for the numerical estimation of ⌬ through the establishment of dimensionless ratios of the type ⌫ X /⌫ H , by experiment and through SCF calculation, as a function of ⌬, for polymer/solvent/ substrate systems characterized by specific combinations of , ps, and N.