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Synthesis of polyethylene-graft-poly(styrene-co-maleic anhydride) and its compatibilizing effects on polyethylene/starch blends

机译:聚乙烯接枝聚(苯乙烯-马来酸酐)的合成及其对聚乙烯/淀粉共混物的增容作用

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摘要

Low density polyethylene (LDPE) was reacted with benzoyl peroxide (BPO) and 2,2,6,6-tetramethyl-1-piperidinyloxy (TEMPO) to prepare a latent macroinitiator, PE-TEMPO. Little polymer was synthesized when maleic anhydride (MAH) was bulk polymerized in the presence of the PE-TEMPO. However, addition of styrene accelerated the polymerization rate and PE-grafted-poly(styrene-co-maleic anhyride) [PE-g-P(ST-co-MAH)] was produced to a high yield. Chemical reaction between MAH units and hydroxyl groups of starch was nearly undetectable in the PE/PE-g-P(ST-co-MAH) /starch blend system, and the tensile properties of the blend were not enhanced significantly. However, addition of tetrabutyl titanate (TNBT) during the blending procedure improved the tensile properties significantly through an increased interfacial adhesion between the components in the blend system. (C) 2003 Wiley Periodicals, Inc. [References: 12]
机译:使低密度聚乙烯(LDPE)与过氧化苯甲酰(BPO)和2,2,6,6-四甲基-1-哌啶基氧基(TEMPO)反应以制备潜在的大分子引发剂PE-TEMPO。当在PE-TEMPO存在下本体聚合马来酸酐(MAH)时,合成的聚合物很少。然而,苯乙烯的加入加速了聚合速率,并且以高收率生产了PE接枝的聚(苯乙烯-马来酸酐共聚物)[PE-g-P(ST-co-MAH)]。在PE / PE-g-P(ST-co-MAH)/淀粉共混体系中,几乎无法检测到MAH单元与淀粉羟基之间的化学反应,并且共混物的拉伸性能没有得到明显提高。但是,在共混过程中添加钛酸四丁酯(TNBT)通过增加共混体系中各组分之间的界面粘合力,显着改善了拉伸性能。 (C)2003 Wiley Periodicals,Inc. [参考:12]

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