Abstract
The relation between crystallinity and miscibility of semicrystalline polymer blends of poly(vinyl isobutyl ether) (PVIBE) and poly(ε-L-lysine) (ε-PL) is investigated by 13C cross-polarization with magic-angle-spinning (CPMAS) NMR (nuclear magnetic resonance) and DSC measurements. Analysis of the 1H spin-lattice relaxation curves observed from both PVIBE and ε-PL signals, which are indirectly obtained from well-resolved 13C CPMAS NMR spectra, suggested that the domains of ε-PL in the blends are in the range of 50–100 nm scale. Two-spin or three-spin models were used to simulate the 1H relaxation curves taking into account the contribution of a 1H spin-diffusion rate between PVIBE and ε-PL. Furthermore, it was found that blending ε-PL largely influences the crystallinity of PVIBE but that of ε-PL is little affected by blending PVIBE except for 10/1 composition. The observed melting point of ε-PL shifted towards lower temperature accompanied by PVIBE content. This shift was explained by the Gibbs-Thomson effect that the decrease of thickness of crystalline phase causes the depression of the melting point.
Solid-state
13C CPMAS NMR spectra and DSC curves for PVIBE/ε-PL blends depending on the compositions.
Fullsize Image
