Switchable surfactants at the polystyrene–water interface: effect of molecular structure

Author:

Su Xin1,Jessop Philip G.2,Cunningham Michael F.23

Affiliation:

1. Postdoctoral fellow, Department of Chemistry, Queen’s University, Kingston, Ontario, Canada

2. Professor, Department of Chemistry, Queen’s University, Kingston, Ontario, Canada

3. Department of Chemical Engineering, Queen’s University, Kingston, Ontario, Canada

Abstract

Polystyrene (PS) latexes prepared with either C12N (N’-dodecyl-N,N-dimethylacetamidinium bicarbonate) or C12E2N (N’-(2-(2-(dodecyloxy)ethoxy)ethyl)-N,N-dimethylacetamidinium bicarbonate) switchable surfactants are stable when CO2 is present, aggregate when CO2 is removed and can be redispersed by readdition of CO2. The surface coverage of the latex with surfactant drops significantly when CO2 is removed. For PS latexes with C12N, the surface coverage does not return to the original value when CO2 is reintroduced, but the coverage of the latex with C12E2N does return to the initial value. The redispersion process of the PS latex with C12E2N occurs much more rapidly when sparging with CO2. Both C12N and C12E2N behave as surfactants in the presence of CO2, but in the absence of CO2, only C12E2N continues to have some surface activity. Due to their different molecular structures, their solid surface adsorption behaviors differ. With or without CO2, C12E2N exhibits monolayer adsorption on the surface of the latex particle.

Publisher

Thomas Telford Ltd.

Subject

Materials Chemistry,Polymers and Plastics,Pollution

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