4.7 Article

Miscibility, Morphology and Crystallization Behavior of Poly(Butylene Succinate-co-Butylene Adipate)/Poly(Vinyl Phenol)/Poly(l-Lactic Acid) Blends

Journal

POLYMERS
Volume 8, Issue 12, Pages -

Publisher

MDPI AG
DOI: 10.3390/polym8120421

Keywords

poly(l-lactic acid); poly(butylene succinate-co-butylene adipate); miscibility; crystallization; hydrogen bonding

Funding

  1. National Natural Science Foundation of China [21264012]
  2. Open Project of Chinese Academy of Sciences Key Laboratory of Engineering Plastics, Institute of Chemistry

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Amorphous poly(vinyl phenol) (PVPh) is introduced into poly(butylene succinate-co-butylene adipate)/poly(l-lactic acid) (PBSA/PLLA) blends via solution casting. Fourier transform infrared spectroscopy (FTIR) analysis verifies that intermolecular hydrogen bonding formed in PBSA/PVPh/PLLA blends. The miscibility between PBSA and PLLA is improved with PVPh incorporation as evidenced by approaching T(g)s of the two components. When PVPh content reaches up to 50 wt %, the blend sample exhibits only one T-g, meaning complete miscibility between PBSA and PLLA. The improved miscibility of PBSA/PLLA blends is further confirmed by scanning electron microscope (SEM). Typical see-island phase separation structure for PBSA/PLLA blend transforms into homogenous phase structure for blend samples with 5 wt % PVPh and above. Non-isothermal crystallization analysis shows that the crystallization temperature and crystallization enthalpy of PBSA decrease with PVPh addition, and those of PLLA also show a decreasing trend. Isothermal crystallization rate of PBSA in blend samples distinctly decreases with PVPh incorporation, whereas that of PLLA in blend samples increases slightly with PVPh addition. Wide angle X-ray diffraction (WAXD) analysis indicated that PLLA in blend samples remained partly crystallized, while PBSA turned into amorphous state with increasing PVPh contents.

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