Lubrication in aqueous solutions using cationic surfactants ? a study of static and dynamic forces

This paper concerns lubrication in aqueous surfactant systems where the surfactants adsorb at surfaces, in relative motion, forming either a surfactant monolayer or a multi- (liquid crystalline) layer. The surfactants were of two kinds, viz., a double chain cationic surfactant, didodecyldimethylammonium bromide, DDAB, and a single chain cationic surfactant, dodecyltrimethylammonium bromide, DTAB. Excellent film forming capability was shown for DDAB and interpreted as the result of good packing of the surfactant molecules at the surfaces, i.e., the inherent ability of the surfactant molecules to form liquid crystalline structures at the surface, resulting in good load-carrying capability. This is also reflected in the bulk properties of the surfactants, where DDAB show lamellar liquid crystalline phases at concentrations much lower than DTAB, which does not show good lubrication properties. The results are discussed in terms of film stability of a surfactant layer adsorbed at the surface, which in turn is correlated to the critical packing parameter of the surfactant, in analogy with the Kabalnov?Wennerström theory of emulsion droplet coalescence (Kabalnov, A.; Wennerström, H. Langmuir 1996, 12, 276). The systems were characterized using (i) the surface force apparatus determining the interaction forces between the adsorbed layers at the surfaces and (ii) the EHD rig (elastohydrodynamic rig) determining film formation under shear. The adsorption kinetics and composition at the surface were determined by a quartz crystal microbalance and X-ray photoelectron spectroscop

Adsorption and onset of lubrication by a double-chained cationic surfactant on silica surfaces

In the context of glass fiber manufacturing the onset of lubrication by a C18 double-chained cationic surfactant has been investigated at high normal contact pressures. Comparison with adsorption kinetics demonstrates that lubrication is not directly connected to the surfactant surface excess but originates from the transition to a defect-free bilayer which generates limited dissipation. The impact of ionic strength and shear rate has also been studied

Adsorption and frictional properties of surfactant assemblies at surfaces.

NR 2014080

Adsorption and frictional properties of surfactant assemblies at surfaces.

NR 2014080