The Effect of Modifier on Electret Properties and Hardness of Epoxy Composite Material

IF 2.9 3区 工程技术 Q2 ENGINEERING, ELECTRICAL & ELECTRONIC
Mansur Galikhanov;Xiaoqing Zhang;Xingchen Ma;Ekaterina Mochalova;Alina Guzhova
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Abstract

The study focuses on the synthesis of thermoelectrets by combining epoxy oligomer, epoxy-urethane modifier (PEF-3A), and polyaminoamide curing agent (L-20) and the influence of the modifier and curing agent on electret properties and mechanical strength. The process involves polymer synthesis through curing the initial oligomer and modifier, as well as polarization in a constant electric field to create the electret state of the polymer dielectrics. The variation of the content (2.5–10.0 wt.%) of the modifier in the composition results in changes in the electret and mechanical characteristics, including surface potential, effective surface charge density, electrostatic field strength, and Shore D hardness. These changes are attributed to the interplay between reduced mobility of polar groups due to strong physical intermolecular interaction in the structure of the network of the 3-D polymer and an increased number of functional groups participating in polarization processes. Increasing the content of modifier PEF-3A in the composition of the basic oligomer DER-331 leads to a decrease in the frequency of the spatial mesh of the resulting 3-D structure due to the incorporation of an epoxy-urethane oligomer with a large molecular weight. The study of DER-331 and L-20 composite by the method of thermally stimulated depolarization (TSD) reveals the process of polymer devitrification and the occurrence of post-curing reactions. The dielectric spectroscopy method proves the dipole macromolecular group orientation of epoxy polymer material, typical for the electret state of polymer dielectrics. According to the calculation data of dielectric relaxation process activation energy, it is concluded that the electret state in the polymeric matrix formed during curing and fixed by the chemical bonds of a 3-D network is a free state of epoxyamine macromolecules. Dipole groups, mostly oriented in one direction, are “frozen” in the cured net structure, acting as thermoelectret charge carriers. An increase in the modifier content does not significantly impact hardness, while polarization results in a marked difference between the Shore D hardness of unpolarized and polarized samples. This difference can be attributed to the orientation of polar groups during the synthesis, which leads to the emergence of a denser mesh of physical bonds. Therefore, by changing the formulation of the epoxy composition, it is possible to regulate its electret and strength properties.
改性剂对环氧树脂复合材料驻极体性能和硬度的影响
研究重点是通过环氧低聚物、环氧聚氨酯改性剂(PEF-3A)和聚酰胺固化剂(L-20)的组合合成热驻极体,以及改性剂和固化剂对驻极体性能和机械强度的影响。该工艺包括通过固化初始低聚物和改性剂来合成聚合物,以及在恒定电场中极化以形成聚合物电介质的驻极体状态。改性剂在组合物中的含量变化(2.5-10.0 wt.%)会导致驻极体和机械特性发生变化,包括表面电位、有效表面电荷密度、静电场强度和肖氏硬度。这些变化归因于三维聚合物网络结构中强烈的物理分子间相互作用导致极性基团的流动性降低和参与极化过程的官能团数量增加之间的相互作用。在基本低聚物 DER-331 的组成中增加改性剂 PEF-3A 的含量,会导致所产生的三维结构的空间网格频率降低,这是由于加入了分子量较大的环氧聚氨酯低聚物。利用热刺激去极化(TSD)方法对 DER-331 和 L-20 复合材料进行的研究揭示了聚合物的蜕变过程和固化后反应的发生。电介质光谱法证明了环氧聚合物材料的偶极大分子基团取向,这是聚合物电介质的典型驻极体状态。根据介电弛豫过程活化能的计算数据,可以得出结论:在固化过程中形成的聚合物基体中,由三维网络化学键固定的驻极体状态是环氧胺大分子的自由状态。大多朝向一个方向的偶极子基团被 "冻结 "在固化的网状结构中,充当热驻极体电荷载体。改性剂含量的增加不会对硬度产生显著影响,而极化则会导致未极化和极化样品的邵氏硬度有明显差异。这种差异可归因于极性基团在合成过程中的取向,从而导致出现更密集的物理键网。因此,通过改变环氧组合物的配方,可以调节其驻极体和强度特性。
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来源期刊
IEEE Transactions on Dielectrics and Electrical Insulation
IEEE Transactions on Dielectrics and Electrical Insulation 工程技术-工程:电子与电气
CiteScore
6.00
自引率
22.60%
发文量
309
审稿时长
5.2 months
期刊介绍: Topics that are concerned with dielectric phenomena and measurements, with development and characterization of gaseous, vacuum, liquid and solid electrical insulating materials and systems; and with utilization of these materials in circuits and systems under condition of use.
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