Fast Drying and Film Formation of Latex Dispersions Studied with FTIR Spectroscopic Imaging

• Published in: Langmuir Vol. 30; no. 45; pp. 13588 - 13595
• Main Authors: Kimber, James A, Gerst, Matthias, Kazarian, Sergei G
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 18.11.2014
• ISSN: 0743-7463; 1520-5827
• DOI: 10.1021/la5035257

Drying of thin latex films (∼20 μm) at high drying speeds (of the order of seconds) has been studied by fast chemical imaging. ATR-FTIR spectroscopic imaging combined with a fast “kinetic” mode was used to acquire spectral images without coaddition, enabling the amount of water and homogeneity of the drying film to be studied over time. Drying profiles, constructed from analyzing the water content in each image, show two stages of drying, a fast and a slow region. The formulation of latex dispersions affects the onset of slow drying and the volume fraction of water remaining at the onset of slow drying. In this work, the effect of physical properties, film thickness and glass transition temperature (T g), were investigated, as well as the effect of monomer composition where two monomoers, 2-ethylhexyl acrylate and n-butyl acrylate, and the amount of hydrophilic comonomer, methyl methacrylate (MMA), were varied. It was found that thicker films produced slower overall drying and that the formulation with a T g above the minimum film formation temperature did not dry evenly, exhibiting cracking. However, the drying kinetics of high and low T g films were similar, highlighting the advantage of using a spatially-resolved spectroscopic approach. Formulations containing more MMA dried faster than those with less. This was due to the hydrophilicity of MMA and the increase in T g of the dispersion from the addition of MMA. Overall, FTIR spectroscopic imaging was shown to be a suitable approach in measuring film drying at high speeds as both chemical changes and chemical distribution could be analyzed over time.