Small-angle neutron scattering and surface tension have been used to characterize a class of surfactants (SURFs), including surfactant ionic liquids (SAILs). These SURFs and SAILs are based on organic surfactant anions (single-tail dodecyl sulfate, DS, double-chain aerosol-OT, AOT, and the trichain, TC) with substituted quaternary ammonium cations. This class of surfactants can be obtained by straightforward chemistry, being cheaper and more environmentally benign than standard cationic SAILs. A surprising aspect of the results is that, broadly speaking, the physicochemical properties of these SURFs and SAILs are dominated by the nature of the surfactant anion and that the chemical structure of the added cation plays only a secondary role.

Natural surfaces can be superhydrophobic, but on the other hand, superoleophobic properties are extremely rare. We demonstrate that modification of the 3,4-alkylenedioxy bridge length in pyrrole-derivative monomers can have a dramatic influence on the superoleophobic properties of electrodeposited conductive polymers. Here we report the synthesis and characterization of novel fluorinated 3,4-ethylenedioxypyrrole (EDOP) and 3,4-propylenedioxypyrrole (ProDOP) monomers and their corresponding electrodeposited polymers. The polymer surfaces were characterized by static and dynamic contact angle measurements, scanning electron microscopy, and cyclic voltammetry. Surprisingly, the antiwetting properties do not depend of the fluorocarbon chain length (F-octyl to F-hexyl) but are in fact governed by the nature of the electrochemically deposited core. Indeed, superhydrophobic and superoleophobic surfaces with extremely low hysteresis and sliding angles for water droplets were obtained by electrochemical polymerization of highly fluorinated EDOP, whereas highly fluorinated ProDOP gave only superhydrophobic surfaces with a sticky behavior. The difference in wettability is attributed to surface nanoporosity resulting from the doping process.

The article addresses an important, and still unresolved question in the field of CO(2) science and technology: what is the minimum fluorine content necessary to obtain a CO(2)-philic surfactant? A previous publication (Langmuir 2002, 18, 3014) suggested there should be an ideal fluorination level: for optimization of possible process applications in CO(2), it is important to establish just how little F is needed to render a surfactant CO(2)-philic. Here, optimum chemical structures for water-in-CO(2) (w/c) microemulsion stabilization are identified through a systematic study of CO(2)-philic surfactant design based on dichain sulfosuccinates. High pressure small-angle neutron scattering (HP-SANS) measurements of reversed micelle formation in CO(2) show a clear relationship between F content and CO(2) compatibility of any given surfactant. Interestingly, high F content surfactants, having lower limiting aqueous surface tensions, γ(cmc), also have better performance in CO(2), as indicated by lower cloud point pressures, P(trans). The results have important implications for the rational design of CO(2)-philic surfactants helping to identify the most economic and efficient compounds for emerging CO(2) based fluid technologies.