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Rapid room-temperature polymerization of bio-based multiaziridine-containing compounds

机译:生物基含有生物的多氮杂化合物的快速室温聚合

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摘要

Successful Michael addition under mild reaction conditions resulted in the grafting of 2-methyl aziridine onto acrylated epoxidized soybean oil, and the aziridine content was titrated as 0.00413 mol g(-1). Multiaziridine-containing acrylated epoxidized soybean oil (AESO-AZ) was then subjected to rapid room-temperature polymerization with succinic acid, citric acid, and an isosorbide-based diacid, respectively. The polyacids were added to AESO-AZ at stoichiometric ratios. The resulting polymeric materials were cast into films in order to investigate their thermo-mechanical properties. Differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA), thermogravimetric analysis (TGA), and tensile stress-strain tests were performed. The glass transition temperatures (T-g) of the samples suggested that increased functionality of the carboxylic acid groups in the polyacids may have effectively increased T-g, while the rigid rings in isosorbide did not have significant impact on T-g. This work illustrates the feasibility of synthesizing bio-based multiaziridine-containing compounds that can be used as the monomer for rapid polymerization with bio-based polyacids at ambient temperature.
机译:在温和的反应条件下成功的迈克尔添加导致将2-甲基氮化辛吡啶接枝到丙烯酸丙烯酸酯化到丙烯酸酯化的豆油中,并滴定吡啶含量为0.00413molg(-1)。然后分别用琥珀酸,柠檬酸和基于异山梨醇基二酸的含含含丙烯酸丙烯酸丙烯酸酯化的氨基氧化豆油(Aeso-AZ)。在化学计量比下将多酸加入到Aeso-Az中。将所得的聚合物材料浇铸成薄膜以研究其热机械性能。差分扫描量热法(DSC),动态机械分析(DMA),热重试验分析(TGA)和拉伸应力 - 应变试验。样品的玻璃化转变温度(T-G)表明,多酸中的羧酸基团的羧酸基团的功能增加可能有效增加T-G,而异山梨醇中的刚性环对T-G没有显着影响。该工作说明了合成生物基多氮胺的化合物的可行性,该化合物可用作在环境温度下用生物基多酸的快速聚合的单体。

著录项

  • 来源
    《RSC Advances 》 |2015年第2期| 共7页
  • 作者单位

    Iowa State Univ Dept Mat Sci &

    Engn Ames IA 50011 USA;

    Iowa State Univ Dept Chem Ames IA 50011 USA;

    Iowa State Univ Dept Mat Sci &

    Engn Ames IA 50011 USA;

    Iowa State Univ Dept Mat Sci &

    Engn Ames IA 50011 USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学 ;
  • 关键词

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