Assembly of Polyethyleneimine in the Hexagonal Mesophase of Nonionic Surfactant: Effect of pH and Temperature
journal contributionposted on 2011-07-28, 00:00 authored by Kamendra P. Sharma, Chandan Kumar Choudhury, Sonal Srivastava, H. Davis, P. R. Rajamohanan, Sudip Roy, Guruswamy Kumaraswamy
We investigate the dispersion of a pH responsive polymer, polyethyleneimine, PEI, in a hexagonal (H1) mesophase of a nonionic surfactant, C12E9, and water, at pH ranging from basic (pH = 12.8) to acidic (pH = 1). While the C12E9/H2O phase behavior is independent of pH, we demonstrate that, in the PEI/C12E9/H2O system, changing the pH influences PEI-C12E9 interactions, and thus, influences the isotropic-H1 phase transition. With decrease in pH, there is increasing protonation of the PEI chain, and consequently, the chain extends. We show, using a combination of SAXs, optical microscopy and visual experiments, that the inclusion of PEI in a 1:1 surfactant–water mixture, lowers the hexagonal-isotropic transition temperature, THI. At higher pH = 12.8, THI shows a pronounced decrease from 50 to 13 °C on addition of PEI, and the PEI/C12E9/H2O system forms a transparent gel. At pH = 1, we observe qualitatively different behavior and an opaque gel forms below THI = 25 °C. The isotropic-H1 transition, in turn, influences the phase separation of PEI chains from the C12E9/H2O system. 2D NMR ROESY data provides evidence that there are strong surfactant–PEI interactions at high pH that significantly reduce at lower pH. The NMR data is in accord with molecular dynamics simulations that show that surfactants strongly aggregate with unprotonated PEI chains, but not with fully protonated chains; thus, in this system, the pH controls a cascade of microstructural organization: increasing pH decreases chain protonation and increases polymer–surfactant interactions, resulting in suppression of the isotropic-H1 transition to lower temperatures, thus, influencing the phase separation of PEI from the surfactant/water system.