A. V. Druzhinina, M. Suleimenova, O. A. Almabekov, A. K. Kusainova
{"title":"SYNTHESIS OF POLYIMIDES OF ARILACYCLIC STRUCTURE","authors":"A. V. Druzhinina, M. Suleimenova, O. A. Almabekov, A. K. Kusainova","doi":"10.51580/2021-1/2710-1185.34","DOIUrl":null,"url":null,"abstract":"The article describes methods for producing polymeric materials based on tetra-carboxylic acid dianhydrides obtained by photochemical or solar irradiation from furan and maleic anhydride. The procedure of synthesis of aryl-alicyclic polyimides based on 7-оxsоdiciklo (2,2,1)-gepten -2,3- dicarboxylic acid(MAF) and diaminodiphenyl oxide diamines (DADFO) and dioxytriphenyldiamine (DOTFDA) in polar aprotic amide-type solvents has been studied in detail in the presence of a basic catalyst type: trimethyl-amine.The nature and reactivity of staring monomers affect the process of obtaining polyimides. The optimal conditions for obtaining polyimides with intrinsic viscosity values of 1.30-1.64 dl/g have been found. Physicochemical, electrical and thermal proper-ties of the synthesized polyimides have been investigated. It was found that they have increased elasticity, high tensile strength. Elongation at break of polyimide films reaches 30-43%, tensile strength is 130-180 MPa. According to their electrical properties, these polyimides are classified as medium-frequency dielectrics. In addition, they differ in thermoplasticity in the range from 210 ºС to 250 ºС, have thermal stability and do not decompose at heating in air to temperatures of 335-390 ºС, and the presence of oxide groups in the structure of polymers increases the solubility of polyimides.","PeriodicalId":9856,"journal":{"name":"Chemical Journal of Kazakhstan","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2021-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Journal of Kazakhstan","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.51580/2021-1/2710-1185.34","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The article describes methods for producing polymeric materials based on tetra-carboxylic acid dianhydrides obtained by photochemical or solar irradiation from furan and maleic anhydride. The procedure of synthesis of aryl-alicyclic polyimides based on 7-оxsоdiciklo (2,2,1)-gepten -2,3- dicarboxylic acid(MAF) and diaminodiphenyl oxide diamines (DADFO) and dioxytriphenyldiamine (DOTFDA) in polar aprotic amide-type solvents has been studied in detail in the presence of a basic catalyst type: trimethyl-amine.The nature and reactivity of staring monomers affect the process of obtaining polyimides. The optimal conditions for obtaining polyimides with intrinsic viscosity values of 1.30-1.64 dl/g have been found. Physicochemical, electrical and thermal proper-ties of the synthesized polyimides have been investigated. It was found that they have increased elasticity, high tensile strength. Elongation at break of polyimide films reaches 30-43%, tensile strength is 130-180 MPa. According to their electrical properties, these polyimides are classified as medium-frequency dielectrics. In addition, they differ in thermoplasticity in the range from 210 ºС to 250 ºС, have thermal stability and do not decompose at heating in air to temperatures of 335-390 ºС, and the presence of oxide groups in the structure of polymers increases the solubility of polyimides.
本文介绍了以呋喃和马来酸酐为原料,光化学或太阳辐照法制备四羧酸二酐聚合物材料的方法。详细研究了在极性非质子酰胺型溶剂中,以7- k - k (2,2,1)-gepten -2,3-二羧酸(MAF)和二氨基二苯基氧化二胺(DADFO)和二氧三苯基二胺(DOTFDA)为原料合成芳基脂环聚酰亚胺的工艺过程。起始单体的性质和反应性影响聚酰亚胺的制备过程。得到了特性粘度为1.30 ~ 1.64 dl/g的聚酰亚胺的最佳工艺条件。研究了合成的聚酰亚胺的理化、电学和热学性能。结果表明,它们具有较高的弹性和抗拉强度。聚酰亚胺薄膜的断裂伸长率可达30-43%,抗拉强度为130- 180mpa。根据它们的电性能,这些聚酰亚胺被归类为中频电介质。此外,它们在210ºС至250ºС范围内的热塑性不同,具有热稳定性,在空气中加热至335-390ºС时不会分解,并且聚合物结构中氧化基团的存在增加了聚酰亚胺的溶解度。