Improving the toughening in poly(lactic acid)-thermoplastic cassava starch reactive blends

被引:23
|
作者
Bher, Anibal [1 ,2 ,3 ]
Auras, Rafael [1 ]
Schvezov, Carlos E. [3 ]
机构
[1] Michigan State Univ, Sch Packaging, E Lansing, MI 48824 USA
[2] UNSAM CNEA, Inst Sabato, San Martin, Buenos Aires, Argentina
[3] UNAM, CONICET, Inst Mat Misiones IMAM, Posadas, Misiones, Argentina
关键词
biodegradable; biopolymers and renewable polymers; compatibilization; thermal properties; thermoplastics; MECHANICAL-PROPERTIES; MALEIC-ANHYDRIDE; THERMOPLASTIC STARCHES; ACID); EXTRUSION; PLA; FUNCTIONALIZATION; PLASTICIZATION; COPOLYMERS; MORPHOLOGY;
D O I
10.1002/app.46140
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Poly(lactic acid) (PLA), a physical blend of PLA and thermoplastic cassava starch (TPCS) (PLA-TPCS), and reactive blends of PLA with TPCS using maleic anhydride as compatibilizer with two different peroxide initiators [i.e., 2,5-bis(tert-butylperoxy)-2,5-dimethylhexane (L101) and dicumyl peroxide (DCP)] PLA-g-TPCS-L101 and PLA-g-TPCS-DCP were produced and characterized. Blends were produced using either a mixer unit or twin-screw extruder. Films for testing were produced by compression molding and cast film extrusion. Morphological, mechanical, thermomechanical, thermal, and optical properties of the samples were assessed. Blends produced with the twin-screw extruder resulted in a better grade of mixing than blends produced with the mixer. Reactive compatibilization improved the interfacial adhesion of PLA and TPCS. Scanning electron microscopy images of the physical blend showed larger TPCS domains in the PLA matrix due to poor compatibilization. However, reactive blends revealed smaller TPCS domains and better interfacial adhesion of TPCS to the PLA matrix when DCP was used as initiator. Reactive blends exhibited high values for elongation at break without an improvement in tensile strength. PLA-g-TPCS-DCP provides promising properties as a tougher biodegradable film. (c) 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018, 135, 46140.
引用
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页数:15
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