从聚对苯二甲酸乙酯PET废料中提取的新型UV固化丙烯酸氨基低聚酯

M. Khedr
{"title":"从聚对苯二甲酸乙酯PET废料中提取的新型UV固化丙烯酸氨基低聚酯","authors":"M. Khedr","doi":"10.21203/rs.3.rs-668530/v1","DOIUrl":null,"url":null,"abstract":"\n The glycolysis products of polyethylene terephthalate (PET) waste represent a potential source for many value-added products that contain terephthalate repeating units in their backbones. Terephthalate repeating units were not attained directly from terephthalic acid due to its high melting point in addition to its tendency to sublime before it reacts. Glycolysis of PET provides an excellent solution for recycling polymer waste and constitutes a substantial starting material for manufacturing materials with high mechanical stress, such as unsaturated polyesters and polyurethane products. In this study, PET was first depolymerized by glycolysis, and glycolyzed products were then dimerized by reaction with toluene di-isocyanate TDI with half equivalence of their hydroxyl groups for the purpose of inserting urethane blocks into the oligomer structure. The remaining half equivalence of terminal hydroxyl groups was modified into acrylate groups by an acrylation reaction. The acrylated oligo urethane ester products were crosslinked with different co-monomers and tested for UV curability and mechanical properties, and they showed outstanding results.","PeriodicalId":22121,"journal":{"name":"Systematic Reviews in Pharmacy","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2021-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"New UV Curable Acrylated Urethane-Oligoesters Derived From Poly(Ethylene Terephthalate) PET Waste\",\"authors\":\"M. Khedr\",\"doi\":\"10.21203/rs.3.rs-668530/v1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\\n The glycolysis products of polyethylene terephthalate (PET) waste represent a potential source for many value-added products that contain terephthalate repeating units in their backbones. Terephthalate repeating units were not attained directly from terephthalic acid due to its high melting point in addition to its tendency to sublime before it reacts. Glycolysis of PET provides an excellent solution for recycling polymer waste and constitutes a substantial starting material for manufacturing materials with high mechanical stress, such as unsaturated polyesters and polyurethane products. In this study, PET was first depolymerized by glycolysis, and glycolyzed products were then dimerized by reaction with toluene di-isocyanate TDI with half equivalence of their hydroxyl groups for the purpose of inserting urethane blocks into the oligomer structure. The remaining half equivalence of terminal hydroxyl groups was modified into acrylate groups by an acrylation reaction. The acrylated oligo urethane ester products were crosslinked with different co-monomers and tested for UV curability and mechanical properties, and they showed outstanding results.\",\"PeriodicalId\":22121,\"journal\":{\"name\":\"Systematic Reviews in Pharmacy\",\"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\":\"Systematic Reviews in Pharmacy\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.21203/rs.3.rs-668530/v1\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Systematic Reviews in Pharmacy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21203/rs.3.rs-668530/v1","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

聚对苯二甲酸乙二醇酯(PET)废物的糖酵解产物代表了许多在其主干中含有对苯二甲酸重复单元的增值产品的潜在来源。由于对苯二甲酸熔点高,而且在反应前容易升华,所以不能直接从对苯二甲酸中得到对苯二甲酸重复单元。PET的糖酵解为回收聚合物废料提供了一种极好的解决方案,并构成了制造高机械应力材料(如不饱和聚酯和聚氨酯产品)的重要原料。在本研究中,PET首先通过糖醇解聚,然后通过与甲苯二异氰酸酯TDI反应,糖醇解产物的羟基是一半相等的,目的是在低聚物结构中插入聚氨酯嵌段。剩余的半等效末端羟基通过丙烯酸化反应修饰成丙烯酸酯基团。用不同的共聚单体交联制备丙烯酸低聚聚氨酯酯产品,并对其紫外光固化性能和力学性能进行了测试。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
New UV Curable Acrylated Urethane-Oligoesters Derived From Poly(Ethylene Terephthalate) PET Waste
The glycolysis products of polyethylene terephthalate (PET) waste represent a potential source for many value-added products that contain terephthalate repeating units in their backbones. Terephthalate repeating units were not attained directly from terephthalic acid due to its high melting point in addition to its tendency to sublime before it reacts. Glycolysis of PET provides an excellent solution for recycling polymer waste and constitutes a substantial starting material for manufacturing materials with high mechanical stress, such as unsaturated polyesters and polyurethane products. In this study, PET was first depolymerized by glycolysis, and glycolyzed products were then dimerized by reaction with toluene di-isocyanate TDI with half equivalence of their hydroxyl groups for the purpose of inserting urethane blocks into the oligomer structure. The remaining half equivalence of terminal hydroxyl groups was modified into acrylate groups by an acrylation reaction. The acrylated oligo urethane ester products were crosslinked with different co-monomers and tested for UV curability and mechanical properties, and they showed outstanding results.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信