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 IEEE Transactions on Dielectrics and Electrical Insulation Pub Date : 2024-08-30 DOI:10.1109/TDEI.2024.3452655
Mansur Galikhanov;Xiaoqing Zhang;Xingchen Ma;Ekaterina Mochalova;Alina Guzhova
{"title":"The Effect of Modifier on Electret Properties and Hardness of Epoxy Composite Material","authors":"Mansur Galikhanov;Xiaoqing Zhang;Xingchen Ma;Ekaterina Mochalova;Alina Guzhova","doi":"10.1109/TDEI.2024.3452655","DOIUrl":null,"url":null,"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.","PeriodicalId":13247,"journal":{"name":"IEEE Transactions on Dielectrics and Electrical Insulation","volume":null,"pages":null},"PeriodicalIF":2.9000,"publicationDate":"2024-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"IEEE Transactions on Dielectrics and Electrical Insulation","FirstCategoryId":"5","ListUrlMain":"https://ieeexplore.ieee.org/document/10659898/","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENGINEERING, ELECTRICAL & ELECTRONIC","Score":null,"Total":0}
引用次数: 0

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.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
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.
期刊最新文献
Table of Contents IEEE Transactions on Dielectrics and Electrical Insulation Publication Information Editorial Electrets and Related Phenomena IEEE Transactions on Dielectrics and Electrical Insulation Information for Authors IEEE Dielectrics and Electrical Insulation Society Information
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1