Thermal properties of water-resistant starch - polyvinyl alcohol films modified with cellulose nanofibers

被引:77
|
作者
Frone, Adriana Nicoleta [1 ]
Nicolae, Cristian Andi [1 ]
Gabor, Raluca Augusta [1 ]
Panaitescu, Denis Mihaela [1 ]
机构
[1] Natl Inst Res & Dev Chem & Petrochem ICECHIM, Polymer Dept, Bucharest 060021, Romania
关键词
Starch; Cellulose nanofibers; Thermal aging; AFM; TGA analysis; WAXY MAIZE STARCH; GLASS-TRANSITION; THERMOPLASTIC STARCH; LOW MOISTURE; MECHANICAL-PROPERTIES; RELATIVE-HUMIDITY; POTATO STARCH; CROSS-LINKING; NANOCOMPOSITES; COMPOSITES;
D O I
10.1016/j.polymdegradstab.2015.10.010
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Starch based materials look promising substitutes for common plastic materials in many applications provided that water resistance and thermal stability are much improved. One attempt to overcome this challenge was shown in this paper. Starch/polyvinyl alcohol films (S/PVA) modified with different amount of cellulose nanofibers (CN) were prepared using one-pot procedure and their thermal behavior and water resistance were studied in relation to morphological aspects and mechanical behavior. Both optical transmittance and AFM nano-level investigation revealed a homogeneous dispersion of CN regardless of their concentration. Tremendous improvement of thermal stability, with about 100 degrees C, was observed in nanocomposites compared to S/PVA. Different mechanisms by which CN may influence the thermal stability were also analyzed. TGA results correlated with PF QNM mapping have shown that CN promoted better interfacial adhesion between components in S/PVA and prevented the elimination of water and glycerol up to 200 degrees C. S/PVA/CN nanocomposites with more than 4 wt% CN were not damaged by hot water for more than five hours and all the nanocomposites showed minor weight loss up to 200 degrees C. These results indicate that S/PVA/CN nanocomposites are suitable substitutes for common plastic materials in packaging industry and agriculture. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:385 / 397
页数:13
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