Macromolecules · 1998 · 32 citations · 34 references
Natural SciencesChemical EngineeringChemistryChemical KineticsPolymer ChemistrySurface ScienceAdsorption At InterfacesAdsorption ProcessesAdsorptive SeparationsSurface AdsorptionSurface KineticsSurface ReactionsAdsorption IsothermsAdsorption MechanismsAdsorption To SurfacesChemical AdsorptionPolymer AdsorptionSurface Adsorption IsothermsSurface Adsorption PhenomenaSurface Excess
The synthesis and labeling (with 35 S) of a water-soluble random copolymer of styrenesulfonate and tert -butylstyrene (20 mol %) is described. Adsorption of this copolymer to the toluene/water interface is followed in situ using a proximity radiometric detection scheme, where the organic phase also serves as a scintillator. Adsorption isotherms, determined with the aqueous phase either salt-free or containing 1 M NaCl, are of the high-affinity type, with respective pseudolimiting adsorbed amounts of 0.24 and 1.4 mg m -2 . Adsorption is fairly rapid, occurring with a time constant of a few minutes. Self-exchange of radiolabeled polymer at the interface, performed with a solution excess of unlabeled polymer, is complete within a few hours, providing evidence that the surface excess is under thermodynamic, rather than kinetic, control. Preliminary comparisons of the liquid/liquid interface and a chemically similar polystyrene/water interface reveal that the adsorption isotherms are similar despite the additional mobility afforded to adsorbed segments at the fluid interface. The free energy of adsorption for tert -butylstyrene units is estimated to be ca. 13 kT from solubility and partitioning measurements of the corresponding monomer.
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