4.7 Article

Crystallization and crystalline dynamics of poly(3-hydroxybutyrate) / poly (4-vinylphenol) polymer blends studied by low-frequency vibrational spectroscopy

Journal

POLYMER
Volume 181, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.polymer.2019.121790

Keywords

poly(3-hydroxybutyrate) (PHB); poly(4-vinylphenol) (PVPh); Terahertz (THz); Far-infrared (FIR); Low-frequency Raman spectroscopy; Hydrogen-bond; Crystallization; Miscibility

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Composition- and temperature-dependent far-infrared (FIR), terahertz (THz), and low-frequency Raman spectra of poly(3-hydroxybutyrate) (PHB)/Poly(4-vinylphenol) (PVPh) polymer blends were measured to investigate the effects of PVPh in PHB crystallization. FIR, low-frequency Raman, and wide angle X-ray diffraction (WAXD) studies revealed that PVPh reduces the crystallinity of PHB in blends without a significant change in the crystal structure. The FIR and low-frequency Raman spectra divided the blends into three categories: high-ordered crystalline, less-ordered crystalline, and amorphous. A new peak was observed at 135 cm(-1) in the FIR spectra of the PHB/PVPh blends, which may be assigned to the less-ordered crystalline phase of PHB, predicting the intermolecular hydrogen-bond interactions of PHB/PVPh. The intensity ratio of the peaks at 97 and 82 cm(-1) changed with the blending ratio variations owing to the crystalline dynamics of PHB. Deformation of the PHB helical structure occurred first, followed by weakening of the intra-molecular hydrogen-bond within PHB. Shifts of several peaks were observed in the FIR and low-frequency Raman spectra, suggesting that the intra-molecular hydrogen-bond (C=O center dot center dot center dot H-C-) within PHB weakened with temperature. The novelty of the present study is to demonstrate that low-frequency vibrational spectroscopy is very sensitive to monitor changes from the intramolecular hydrogen bonding to inter-molecular hydrogen bonding between PHB and PVPh.

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