The baking temperature (Tb) of an epoxy resin was optimized in order to decrease the dynamic interfacial tension, identifying the lowest wettability conditions for liquids flowing at a high rate. The dependence of dynamic interfacial tension on Tb was evaluated for the diglycidyl ether of bisphenol A. This resin was used to coat a sucking rod at the oil field of Bacia de Sergipe/Alagoas, Brazil in order to reduce blockage occurrences, maintenance stops, and the pumping capacity required. The samples were baked for 24 h between 100 and 180°C. Their color and absorption spectra showed progressive dependence of Tb, indicating a migration from polymerization, through polymer network degradation, until carbonization. Spectrofluorimetry showed an initial increase in the energy gap between absorption and emission followed by a decrease that was attributed to changes of the chemical environment isotropy. Fourier transform infrared spectroscopy showed that the maximum polymerization occurred at 140°C. Dynamic interfacial tension was evaluated by fluorescence depolarization of induced flowing liquids, using polarized laser-induced fluorescence within induced liquid flows and was clearly dependent on Tb. The lowest dynamic wettability was at 120°C, just before full polymerization, which was attributed to two competing effects as Tb increased: polymerization and progressive yielding of compounds from the epoxy degradation. This points to the need to review the standard application procedures of these resins.