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Modification of epoxy resins with thermoplastic segmented polycarbonate-based polyurethanes

机译:用热塑性嵌段聚碳酸酯基聚氨酯改性环氧树脂

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In this work, epoxy hybrid materials were synthesized by addition of thermoplastic segmented aliphatic polyurethanes with good elastic properties. The modified epoxy samples were obtained by curing of previously homogenized mixture of prepared polyurethane melts, epoxy resin and crosslinking agent Jeffamine D-2000. The influence of different weight content of polyurethanes (5, 10 and 15 wt. % compared to pure epoxy resin) as well the influence of different hard segments of elastomers (20, 25 and 30 wt. %) on the curing of modified epoxy systems was studied. The curing was followed by differential scanning calorimetry (DSC), in dynamic regime from 30 to 300°C, at three heating rates (5, 10 and 20°C/min). With the increase of hard segments content of polyurethanes added in higher concentration (10 and 15 wt. %) into epoxy matrix, the temperature of maximum ratio of curing was shifted to lower values (from 205 to 179°C). Obtained DSC data were analyzed using two integral methods (Ozawa-Flynn-Wall and Kissinger-Akahira-Sunose) and one differential kinetic model (Friedman). The significant differences were observed in the second part of the epoxy curing (for the reaction degrees higher than 60 %), where the values of activation energies remarkably increase. The addition of polyurethane elastomers retarded the curing process due to decreased mobility of reactant molecules caused by higher viscosity of reaction mixture. By detailed analysis of determined kinetic parameters, it is concluded that the influence of slow diffusion is more pronounced in the presence of thermoplastic polycarbonate-based polyurethanes, which confirmed their effect on the mechanism of epoxy curing. The highest tensile strength and hardness showed the DGEBA modified with the polyurethane with highest hard segment content. Increasing the hard segment content of polyurethane and its concentration in matrix, the tensile strength of modified epoxy was increased. The elongation at break of modified epoxy samples was significantly improved by addition of polycarbonate-based polyurethanes with low hard segment content, due to higher content of flexible soft segment chains. [Projekat Ministarstva nauke Republike Srbije, br. III 45022), i Pokrajinski Sekretarijat za nauku i tehnolo?ki razvoj (projekat 114-451-2396/2011-01). Autor iz Praga duguje zahvalnost ?the Grant Agency of the Czech Republic“ (Czech Science Foundation, project No. P108/10/0195).]
机译:在这项工作中,通过添加具有良好弹性的热塑性链段脂族聚氨酯合成了环氧杂化材料。改性的环氧树脂样品是通过将制备的聚氨酯熔体,环氧树脂和交联剂Jeffamine D-2000的预先均质的混合物固化而获得的。聚氨酯的不同重量含量(与纯环氧树脂相比为5、10和15 wt。%)的影响以及弹性体的不同硬链段(20、25和30 wt。%)对改性环氧体系固化的影响被研究了。固化之后,在三种加热速率(5、10和20°C / min)下,在30至300°C的动态范围内进行差示扫描量热法(DSC)。随着以较高浓度(10和15wt。%)添加到环氧基质中的聚氨酯的硬链段含量的增加,最大固化率的温度移至较低的值(从205至179℃)。使用两种积分方法(Ozawa-Flynn-Wall和Kissinger-Akahira-Sunose)和一种微分动力学模型(Friedman)分析获得的DSC数据。在环氧固化的第二部分(反应度高于60%)中观察到显着差异,其中活化能值显着增加。由于反应混合物的较高粘度导致反应物分子的迁移率降低,因此聚氨酯弹性体的添加延迟了固化过程。通过对确定的动力学参数的详细分析,可以得出结论,在热塑性聚碳酸酯基聚氨酯的存在下,缓慢扩散的影响更为明显,这证实了它们对环氧固化机理的影响。最高的拉伸强度和硬度表明DGEBA被具有最高硬链段含量的聚氨酯改性。增加聚氨酯的硬链段含量及其在基体中的浓度,可以提高改性环氧树脂的拉伸强度。通过添加具有低硬链段含量的聚碳酸酯基聚氨酯,由于较高的柔性软链段含量,改性环氧树脂样品的断裂伸长率得到了显着改善。 [Projekat Ministarstva nauke Republike Srbije,br。 III 45022),我的个人语言和个人语言(projekat 114-451-2396 / 2011-01)。 Autor iz Praga duguje zahvalnost是“捷克共和国的资助机构”(捷克科学基金会,项目编号P108 / 10/0195)。

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