These studies focus on behavior of sodium dioctylsulfosuccinate (SDOSS) surfactant
molecules in styrene/n-butyl acrylate/glycidyl methacrylate (Sty/nBA/GMA) and styrene/n-butyl acrylate/methacrylic acid (Sty/nBA/MAA) blended latexes during their film formation process. Using a combination
of Fourier transform infrared (FT-IR) microanalysis and FT-Raman techniques, not only stratification of
SDOSS surfactant molecules during film formation process can be assessed but also the effect of latex
particle structures and cross-linking reactions during coalescence can be determined. For Sty/nBA/GMA
and Sty/nBA/MAA blended copolymer latexes, SDOSS exhibit nonuniform distributions at the film air
(F−A) interface. However, for core/shell Sty/nBA-GMA and Sty/nBA-MAA blended latexes, SDOSS is
distributed uniformly near the F−A interface, and its concentration levels are lower as compared to
copolymer latex blends. At elevated coalescence temperatures, SDOSS migration to the F−A interface is
prohibited due to cross-linking reactions between epoxy and acid groups. Microanalysis results show
that SDOSS migration to the F−A interface is initiated after the majority of H2O (>95%) evaporates
from the film. Furthermore, these studies show that latex particle surface morphology, particle−particle
interdiffusion, and cross-linking reactions play a significant role in controlling mobility of low molecular
weight species in latex films.