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Side Chain Extension of Polypropylene by Aliphatic Diamine and Isocyanate

机译:脂族二胺和异氰酸酯聚丙烯的侧链延伸

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摘要

A post-reaction modification of polypropylene by which to obtain increased melt strength is by reactive extrusion of randomly functionalized PP with polyfunctional monomers. In this study, reactive melt processing of maleated polypropylene (PP-g-MA) with poly[methylene (phenylene isocyanate)] (PMPI), hexamethylene diamine (HMDA), and poly(propylene glycol)-bis-(2-propylamine) (Jeffamine D-400) was carried out. The resulting chain-extended PP-g-MA was confirmed by FTIR analysis. Its thermal and rheological properties were also measured. HMDA and D-400 react with both the carboxylic acid and anhydride form of MA. Though PMPI only reacts with the carboxylic acid of MA, PP-g-MA reacted with PMPI has higher gel content and storage modulus compared to PP-g-MA reacted with the amine. This is because of the higher functionality of PMPI and localized reaction between the isocyanate in PMPI and the carboxylic acid in PP-g-MA.
机译:通过其获得增加的熔体强度的聚丙烯的后反应改性是通过具有多官能单体随机官能化PP的反应性挤出。在该研究中,用聚巯基(PP-G-MA)的活性熔融加工(PP-G-MA),具有聚[亚甲基(亚苯基异氰酸酯)](PMPI),六亚甲基二胺(HMDA)和聚(丙二醇) - (2-丙二醇) (jeffamine d-400)进行了。通过FTIR分析证实得到的链扩展的PP-G-MA。还测量了其热和流变性质。 HMDA和D-400与羧酸和酸酐的MA反应。尽管PMPI仅与MA的羧酸反应,与PP-G-MA与PP-G-MA与胺反应相比,与PMPI反应的PP-G-MA具有更高的凝胶含量和储存模量。这是因为PP-G-mA中的氨基酯与PP-G-MA中的异氰酸异氰酸酯之间的局部反应较高。

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