Molecular and mechanical properties of hydroxypropyl methylcellulose solutions during the sol:gel transition

Abstract

This paper outlines the latest findings in our work to understand the fundamental interactions within hydrated hydroxypropyl methylcellulose (HPMC) at elevated temperature. ATR-FTIR spectroscopy was used to relate molecular interactions to the rheological changes in aqueous HPMC solutions during the sol:gel transition. Sol:gel transition temperatures determined using ATR-FTIR spectroscopy, oscillatory rheology and turbidimetry were in agreement to within experimental error. ATR-FTIR spectroscopy provided direct evidence of increased hydrophobic interactions within the gel network through a shift to lower wavenumber of νas(CH) vibrations observed during the gelation process. In addition, the FTIR spectra provide evidence that the structure of the polymer network is different in the thermo-formed gel, to that which exists in viscous solution. Both the rheological and ATR-FTIR data confirmed the supposition that thermal gelation is a two stage process. The first stage has been attributed to the disruption of native cellulosic bundles and this is supported by the changes in both the storage modulus and intensity of the ν(CO) band at low temperatures. The second stage corresponded to phase separation and gelation resulting from increased hydrophobic interactions between polymer chains at elevated temperatures.