Dynamic Surface Tension and Its Diffusional Decay of Dodecyl Ethoxylates with Different Homologue Distribution

Abstract Dynamic surface tension and its diffusional decay have been studied with four different polydisperse C 12 E 7 at different temperatures and different concentrations. The CMC and the headgroup area from equilibrium surface tension were shown with polydispersity and temperature. The chain length of oxyethylene on the surface was derived from comparison between the headgroup area of monodisperse dodecyl ethoxylates and that of polydisperse C 12 E 7 . The values for ( D eff / D ) were deduced with a diffusion-controlled adsorption model using parameters obtained from equilibrium surface tension. It was shown at short adsorption time that molecules were really adsorbed onto the surface in a diffusion-controlled manner. At a comparably long adsorption time, the ratios ( D eff / D ) were calculated by assuming the selective adsorption onto the surface. The modified Arrhenius-type equation was proposed by putting a concentration term in front of the exponential terms. The modified Arrhenius-type equation gave E a =30 kJ/mole for this system. E a directly derived without an Arrhenius plot was between 9 to 11 kJ/mole. It was an indication that the activation energy alone was not enough to explain the decay of dynamic surface tensions.