Steady-state fluorescence depolarization has proven, in the past few years, to be a method sensitive to adhesion
of thin liquid films flowing without boundaries on solid substrates of different chemical constitutions. This
work extends our prior preliminary assessment of the efficiency of the method and the influence of experimental
variables. Ten thin films of ethylene glycol (MEG) were mapped over 102 mm2 by polarized laser-induced
fluorescence (PLF−FI) while flowing on substrates. The interfacial tension, ΓSL, was varied either by changing
the chemical constitution of the substrate (borosilicate, tin dioxide, poly(vinyl alcohol) (PVA), and linear
alkylbenzene sulfonate (LAS)) or by addition of tensoactives to MEG (sodium dodecyl sulfate (SDS) and
poly(ethylene oxide) (PEO)). Contact angle measurements were employed to classify interfaces according to
their static ΓSL, that is, their wetting efficiencies. PLF−FI experimental variables, such as laser power, film
thickness, and impinging velocity profile, did not alter the data within the range studied, except for flow rates
over 220 cm s-1. Average polarization (P
av) increased from 10.5% to 13.5% upon decreasing adhesion by
varying the chemical constitution of the solid. When surfactants were dissolved in the liquid flow, polarization
ranged from 5.4% to 3.8% while for surfactant as substrate it increased. Simple multivariate principal component
analysis (PCA) was applied to downstream polarization averages (P
down) for each map. The two principal
components accounted for 95.6% of the variance, ordering the maps according to decreasing adhesion and
gathering them into three groups: dissolved surfactants, liquid films flowing at the highest flow rate, and
solid surfaces of different chemical composition. Hierarchic cluster analysis (HCA) showed that, as adhesion
decreased, similarity among the polarization maps increased.