Study on bulk preparation and properties of click chemistry end-crosslinked copolyether elastomers. (May 2016)

• Record Type: Journal Article
• Authors: Zhai, Jinxian; Zhang, Ning; Guo, Xiaoyan; He, Jiyu; Li, Dinghua; Yang, Rongjie
• Is Part Of: European polymer journal. Volume 78(2016:May)
• Page Start: 72
• Page End: 81
• Publication Date: 2016-05
• Subjects: Bulk click chemistry -- ATPET elastomer -- Mechanical properties -- Network model -- Thermal stability; Polymers -- Periodicals; Polymerization -- Periodicals; Polymères -- Périodiques; Polymérisation -- Périodiques; Polymerization; Polymers; Periodicals; Electronic journals; 547.705
• DOI: 10.1016/j.eurpolymj.2016.03.009
• Languages: English
• ISSNs: 0014-3057

Abstract

Graphical abstract: Highlights: Terminal structure has a great influence on copolyether viscosity. Prepared end-crosslinked elastomers by bulk CuAAC under ambient condition. Constructed network models of CuAAC end-crosslinked copolyether elastomers. Elastomer thermal stability depends on polyether strands, but crosslinking points. Abstract: Azide terminated ethylene oxide-tetrahydrofuran copolymer (ATPET) has been prepared through ethylene oxide-tetrahydrofuran copolymer (PET) end-capping modification. The FTIR and 13 C NMR results indicate that the PET terminal hydroxyl was thoroughly replaced and yielded the target product ATPET with a theoretical azide content of 0.464 mmol g −1 . In comparison with PET, ATPET has lower viscosity. Using tripropargylamine as a cross-linker, elastomers with various functional molar ratios (R) were prepared by bulk CuAAC reaction. Mechanical tests indicate that with the increase in R, the mechanical properties exhibit a parabolic dependence on R. Swelling tests demonstrate that the apparent molecular weight of the elastomer effective elastic strands first decreases and subsequently increases with the increase in R. The dynamic mechanical analysis (DMA) reveals that the glass transition temperature of the elastomers is approximately −66 °C. When R < 1.0, dangling strands are formed in the elastomers and cause a higher dissipation factor tan δ . Combined swelling with DMA, the network model of the elastomers is depicted. In addition, the elastomer thermal stability has also been studied.