Inverse gas chromatography (IGC) is a method very well used by the adhesion community for obtaining thermodynamic and morphological information on a variety of materials such as fillers, pigments, colloids, fibers, powder, wood, and polymers [17,60,61,85-94]. The term ‘‘inverse’’ means that the stationary phase is of interest by contrast to conventional gas chromatography in which the mobile phase is of interest. Its success lies in the fact that it is simple, versatile, usable over a very wide range of temperature, and very low cost. IGC has a well established background for the assessment of and acid-base parameters for polymers and fillers. Such thermodynamic parameters can be further used to estimate the reversible work of adhesion at polymer-fiber and polymer-filler interfaces [95,96].
IGC is based on the interfacial interactions between molecular probes and the stationary phase. Probes are injected at infinite dilution so that lateral probe-probe interactions are negligible and the retention is governed by solid-probe interactions only. The net retention volume, VN, is defined as the volume of inert carrier gas (corrected for the dead volume) required to sweep out a probe injected in the chromatographic column. At infinite dilution (zero coverage), AGa, the free energy of adsorption of 1 mole of solute from a reference state, is related to VN by
-AGa = RT ln (27)
&тло J
where R is the gas constant, T the column temperature, P0 the partial pressure of the solute, л0 the two-dimensional spreading pressure of the adsorbed film, and S and m the
specific surface area and mass of the stationary phase, respectively [97]. Dispersive and acid-base properties of materials (e. g., polymers, fibers, and fillers) are deduced from AGa or simply RT ln(VN) data.