Molecular weight effect on the complexation of poly(methacrylic acid) and poly(ethylene oxide) as studied by high-resolution solid-state 13C NMR spectroscopy

Abstract

Complexes of poly(methacrylic acid) (PMAA) and poly(ethylene oxide) (PEO) with different PEO molecular weight were studied by solid-state high-resolution 13C NMR spectroscopy, with the emphasis on the PEO molecular weight effect on inter-polymer interaction, morphology and molecular motion. It is found that the crystalline phase of PEO is completely destroyed in the complex. The results of 1H transverse relaxation times and 13C spin-lattice relaxation times indicate that the chain mobility of both PEO and PMAA are greatly restricted by inter-molecular hydrogen-bonding interactions, especially when the molecular weight of PEO is 1500. The bulk structures of the complexes are found to be closely dependent on the molecular weight of PEO. The fraction of “free” PEO segments without forming hydrogen-bonds with PMAA increases with increasing PEO molecular weight.