Super-tough biodegradable poly(vinyl alcohol)/poly(vinyl pyrrolidone) blends plasticized by glycerol and sorbitol

被引:21
作者
Boonsuk, Phetdaphat [1 ]
Kaewtatip, Kaewta [1 ]
Chantarak, Sirinya [1 ]
Kelarakis, Antonios [2 ]
Chaibundit, Chiraphon [1 ]
机构
[1] Prince Songkla Univ, Dept Mat Sci & Technol, Fac Sci, Hat Yai 90110, Songkhla, Thailand
[2] Univ Cent Lancashire, Ctr Mat Sci, Sch Phys Sci & Comp, Preston PR1 2HE, Lancs, England
关键词
biodegradable; biopolymers and renewable polymers; differential scanning calorimetry; GLASS-TRANSITION TEMPERATURES; OF-THE-ART; MECHANICAL-PROPERTIES; POLYVINYL PYRROLIDONE; HALLOYSITE NANOTUBES; OXYGEN PERMEABILITY; OPTICAL-PROPERTIES; BINARY BLENDS; FILMS; ALCOHOL);
D O I
10.1002/app.46406
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Tough biodegradable films were prepared using a poly(vinyl alcohol) (PVA)/poly(vinyl pyrrolidone) (PVP) (1:1) blend with plasticizers of glycerol (GLY), sorbitol (SOR), and their (one to one) mixture. We studied the effect of plasticization on the structural, thermal, and mechanical properties of the PVA/PVP blend films. Fourier transform infrared spectra indicated good miscibility of the two components due to the H-bonding between the PVA and PVP molecules. The addition of plasticizers reduced the interaction between PVA and PVP, evidenced by an increase in the intensity of PVA diffraction peaks observed in the X-ray diffraction (XRD) characterization. Thermal degradation of the blends increased as a function of the plasticizer used. GLY affected thermal degradation more than SOR and the mixtures. The incorporation of the plasticizers promoted the growth of PVA crystals as evidenced by XRD patterns and the enthalpy of fusion (H-f) obtained by differential scanning calorimetry measurements. The introduction of SOR to the binary blend increased toughness seven times and imparted simultaneous and pronounced improvements to maximum tensile stress and elongation at break. This behavior holds out great promise for the development of a new generation of mechanically robust, yet thoroughly biodegradable materials that could effectively supplant conventional polymers in demanding applications. (c) 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018, 135, 46406.
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页数:8
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