材料科学
共聚物
结晶度
高分子化学
聚砜
层状结构
差示扫描量热法
结晶
共聚酯
无定形固体
玻璃化转变
对苯二甲酸二甲酯
相(物质)
酯交换
动态力学分析
化学工程
聚合物
复合材料
聚酯纤维
结晶学
有机化学
化学
热力学
催化作用
工程类
物理
作者
Joseph M. Dennis,Gregory B. Fahs,Nicholas G. Moon,Ryan J. Mondschein,Robert B. Moore,Garth L. Wilkes,Timothy E. Long
出处
期刊:Macromolecules
[American Chemical Society]
日期:2017-06-22
卷期号:50 (13): 5107-5113
被引量:10
标识
DOI:10.1021/acs.macromol.7b00557
摘要
A facile synthesis of hydroxyethyl-functionalized poly(ether sulfone) (PESu) oligomers permitted subsequent melt transesterification into segmented block copolymers with poly(butylene terephthalate). The unique solubility of the PESu oligomers in the melt with 1,4-butanediol and dimethyl terephthalate enabled a systematic study of segment length on thermomechanical properties of the resulting block copolymers. 1H NMR spectroscopy revealed a compositional dependence on the average segment length of the PBT. Additionally, the concert of NMR spectroscopy, DSC, and DMA highlighted critical segment lengths for crystallization and phase separation. In agreement with a relatively constant Tm and phase separation observed with DSC and DMA, respectively, small-angle X-ray scattering identified a compositionally independent lamellar thickness, while the amorphous layer thickness increased with PESu incorporation. As a result, the complementary analytical techniques provided an understanding of the morphological influence on the thermomechanical behavior of an unprecedented family of high-Tg, semicrystalline, segmented block copolymers.
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