FT-IR spectroscopic study of hydrogen bonding in PA6/clay nanocomposites

Fourier transform infrared spectroscopy was used to investigate PA6/clay nanocomposites (PA6CN) with various cooling histories from the melt, including rapid cooling (water-quenched), middle-rate cooling (air-cooling) and slow cooling (mold-cooling). In contrast to pure PA6 dominated by the α-phase, the addition of clay silicate layers favor the formation of the γ-crystalline phase in PA6CN. us on the reason why silicate layers favor the formation of γ-phase in PA6. Vaia et al. suggested that the addition of clay layers forces the amide groups of PA6 out of the plane formed by the chains. This results in conformational changes of the chains, which limits the formation of H-bonded sheets so that the γ-phase is favored. If this assumption is correct, PA6CN is expected to show some differences as compared with PA6 with respect to hydrogen bonding. licate layers were indeed found to weaken the hydrogen bonding both in the α- and γ-phases. This was also confirmed by X-ray diffraction studies. The γ-phase is most likely concentrated in regions close to the silicate layers, whereas the α-phase is favored in the bulk matrix.