Comparison of surface structures of poly(ethyl methacrylate) and poly(ethyl acrylate) in different chemical environments

Abstract

Sum frequency generation (SFG) vibrational spectroscopy has been applied to investigate and compare the chemical structures of poly(ethyl methacrylate) (PEMA) and poly(ethyl acrylate) (PEA) in air, in water, and in a non-polar solvent, FC-75. SFG spectra from both polymer surfaces in air are dominated by vibrational modes from the ester ethyl side groups. The average orientation of these ester ethyl groups on the two polymer surfaces is slightly different. In water, the two polymers show markedly different restructuring behavior. The ester ethyl side chains on the PEMA surface in water reorient to tilt more toward the surface, yet remain ordered. Such a restructuring of the PEMA surface in water is reversible. However, no SFG signal was detected from the PEA/water interface, showing that the surface of PEA becomes disordered upon contacting water, and this process is irreversible. SFG results collected from the C=O range indicate that hydrogen bonding is observed for both polymer/water interfaces, but the order of C=O at the PEA/water interface is much lower than that at the PEMA/water interface. Supplemental experiments support our hypothesis that the PEA surface becomes rough and loses order gradually as it interacts with water. We have demonstrated, for the first time, that the loss of surface structural order is due to the interaction between soft PEA chains with water molecules followed by reorganization of the polymer backbone. This causes the polymer surface to become rough and disordered. However, the surface structures of PEMA and PEA in FC-75 are similar and are also similar to those in air. This indicates that not only T(g), but also the contacting medium plays an important role in determining the surface restructuring behavior of polymer materials.