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Kinetics of Cross-Linking Reaction of Epoxy Resin with Hydroxyapatite-Functionalized Layered Double Hydroxides

机译:环氧树脂与羟基磷灰石官能化层双氢氧化物交联反应的动力学

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摘要

The cure kinetics analysis of thermoset polymer composites gives useful information about their properties. In this work, two types of layered double hydroxide (LDH) consisting of Mg2+ and Zn2+ as divalent metal ions and CO32− as an anion intercalating agent were synthesized and functionalized with hydroxyapatite (HA) to make a potential thermal resistant nanocomposite. The curing potential of the synthesized nanoplatelets in the epoxy resin was then studied, both qualitatively and quantitatively, in terms of the Cure Index as well as using isoconversional methods, working on the basis of nonisothermal differential scanning calorimetry (DSC) data. Fourier transform infrared spectroscopy (FTIR) was used along with X-ray diffraction (XRD) and thermogravimetric analysis (TGA) to characterize the obtained LDH structures. The FTIR band at 3542 cm−1 corresponded to the O–H stretching vibration of the interlayer water molecules, while the weak band observed at 1640 cm−1 was attributed to the bending vibration of the H–O of the interlayer water. The characteristic band of carbonated hydroxyapatite was observed at 1456 cm−1. In the XRD patterns, the well-defined (00l) reflections, i.e., (003), (006), and (110), supported LDH basal reflections. Nanocomposites prepared at 0.1 wt % were examined for curing potential by the Cure Index as a qualitative criterion that elucidated a Poor cure state for epoxy/LDH nanocomposites. Moreover, the curing kinetics parameters including the activation energy (Eα), reaction order, and the frequency factor were computed using the Friedman and Kissinger–Akahira–Sunose (KAS) isoconversional methods. The evolution of Eα confirmed the inhibitory role of the LDH in the crosslinking reactions. The average value of Eα for the neat epoxy was 54.37 kJ/mol based on the KAS method, whereas the average values were 59.94 and 59.05 kJ/mol for the epoxy containing Zn-Al-CO3-HA and Mg Zn-Al-CO3-HA, respectively. Overall, it was concluded that the developed LDH structures hindered the epoxy curing reactions.
机译:热固性聚合物复合材料的固化动力学分析提供了有关其性质的有用信息。在这项工作中,用羟基磷灰石(HA)合成并官能化由Mg 2 +和Zn2 +组成的两种类型的层状双氢氧化物(LDH),作为二价金属离子和CO32-作为阴离子插入剂。用羟基磷灰石(HA)官能化,使潜在的热阻纳米复合材料。然后在固化指数方面对环氧树脂中合成的纳米孔的固化电位进行定性和定量,以及使用异阳型方法,基于非等热差分扫描量热法(DSC)数据。傅里叶变换红外光谱(FTIR)与X射线衍射(XRD)和热重分析(TGA)一起使用,以表征获得的LDH结构。在3542cm-1处的FTIR带对应于层间水分子的O-H拉伸振动,而在1640cm-1处观察到的弱带归因于中间水的H-O的弯曲振动。在1456cm-1中观察到碳酸羟基磷灰石的特征带。在XRD模式中,定义的(001)反射,即(003),(006)和(110),支持LDH基础反射。在0.1wt%制备的纳米复合材料被固化指数的固化电位作为定性标准,阐明了环氧/ LDH纳米复合材料的差的固化状态。此外,使用弗里德曼和基辛格-Akahira-Sunose(KAS)异组方法计算包括激活能量(Eα),反应顺序和频率因子的固化动力学参数。 Eα的演变证实了LDH在交联反应中的抑制作用。基于KAS法,整个环氧树脂的Eα的平均值为54.37kJ / mol,而含有Zn-Al-Co3-Ha和Mg Zn-Al-Co3-的环氧树脂,平均值为59.94和59.05kJ / mol HA分别。总体而言,它的结论是,发育的LDH结构阻碍了环氧树脂固化反应。

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