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Compatibilization of the poly(lactic acid)/ poly(propylene carbonate) blends through in situ formation of poly(lactic acid)-b-poly(propylene carbonate) copolymer

机译:聚(乳酸)/聚(碳酸亚丙酯)的相容化通过原位形成聚(乳酸)-B-聚(丙烯酸丙酯)共聚物

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The in situ formation of poly(lactic acid)-b-poly(propylene carbonate) (PLA-b-PPC) block copolymers were carried out by the reaction between PLA and PPC in the presence of tetrabutyl titanate via transesterification. Molecular weight measurements and 13 C nuclear magnetic resonance spectroscopy revealed that PLA-b-PPC block copolymers with higher molecular weight were obtained by controlling the reactivity point ratio between PLA chains and PPC chains in PLA/ PPC reaction system. The sample with a composition of PLA: PPC540: 60 (wt %) and a catalyst amount of 0.5 wt % had a more proportionable reactivity point ratio between PLA chains and PPC chains compared with other samples, resulting in a most conspicuous transesterification and inconspicuous chain scission reaction. Therefore, its high molecular weight fraction (Mw> 40.0 3 10 4) increased 80%. The formation of macromolecular PLA-b-PPC copolymer could strengthen the entanglement between PLA and PPC molecular chains, which resulted in an increased viscosity of blends at low shear rate. In addition, the elongation at break of sample with a composition of PLA: PPC540: 60 (wt %) and a catalyst amount of 0.5 wt % was nearly as twice as which without catalyst because of the improving miscibility of PLA domains and PPC matrix by the compatibilization of PLA-b-PPC copolymer. (C) 2017 Wiley Periodicals, Inc.
机译:通过PLA和PPC在通过酯交换的四丁酯存在下的反应来进行聚(乳酸)-B-聚(碳酸丙酯)(PLA-B-PPC)嵌段共聚物进行的原位形成。分子量测量和13 C核磁共振光谱显示,通过在PLA / PPC反应系统中控制PLA链和PPC链之间的反应性点比来获得具有较高分子量的PLA-B-PPC嵌段共聚物。具有PLA组合物的样品:PPC540:60(重量%)和0.5wt%的催化剂量在与其他样品相比,PLA链和PPC链之间的反应性点比具有更大的反应性点比,导致最显着的酯交换和不显眼的链轻轻反应。因此,其高分子量级分(MW> 40.0 3 10 4)增加了80%。大分子PLA-B-PPC共聚物的形成可以增强PLA和PPC分子链之间的缠结,从而导致低剪切速率的共混物的粘度增加。此外,具有PLA组合物的样品中断的伸长率:PPC540:60(WT%)和0.5wt%的催化剂量几乎与催化剂的两倍几乎是由于提高PLA结构域和PPC基质的溶剂PLA-B-PPC共聚物的相容化。 (c)2017 Wiley期刊,Inc。

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