Poly(butylene succinate-co-adipate) Green Composites with Enhanced Rigidity: Influences of Dimension and Surface Modification of Kenaf Fiber Reinforcement

被引:10
作者
Chiu, Fang-Chyou [1 ]
Hsieh, Yu-Chi [1 ]
Sung, Yi-Ching [2 ]
Liang, Nai-Yun [2 ]
机构
[1] Chang Gung Univ, Dept Chem & Mat Engn, Taoyuan 333, Taiwan
[2] Taiwan Text Res Inst, Polymer Mat Sect, New Taipei 236, Taiwan
关键词
POLYLACTIC ACID; MECHANICAL-PROPERTIES; MELTING BEHAVIOR; NANOCOMPOSITES; BIOCOMPOSITES; BIODEGRADABILITY; CRYSTALLIZATION; BIOMATERIALS; SUCCINATE); ORGANOCLAY;
D O I
10.1021/acs.iecr.5b03384
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Kenaf fibers (KFs) were utilized as reinforcements to prepare poly(butylene succinate-co-adipate) (PBSA) green composites. Untreated KFs of KF35 (large dimension) and KF120 (small dimension) imparted the nucleation effect for PBSA crystallization. KF120 exhibited superior nucleation efficiency compared with KF35. The tensile/flexural moduli of PBSA drastically increased after the addition of KF35 or KF120. Successful modifications of KF35 through NaOH(aq) and 3-aminopropyltriethoxysilane (APS) were confirmed. The APS-treated KF (KF35AS) exhibited enhanced interaction with the PBSA matrix compared with NaOH-treated (KF35A) and untreated KF35. KF35A and KF35AS also facilitated the nucleation of PBSA crystallization. The KF3SAS-incorporated composites exhibited the highest tensile/flexural moduli among the different KF-added systems at identical loadings. The tensile and flexural moduli increased to 629% and 360% (40 wt % loading), respectively, compared with PBSA. The enhanced interfacial interaction between KF35AS and PBSA lessened the negative influence of KFs on the thermal stability and water absorption of PBSA.
引用
收藏
页码:12826 / 12835
页数:10
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