个人信息Personal Information
副教授
博士生导师
硕士生导师
主要任职:Null
性别:男
毕业院校:大连理工大学
学位:博士
所在单位:化工学院
学科:高分子材料. 高分子化学与物理
办公地点:西部校区化工实验楼A306
联系方式:13841142437
电子邮箱:zywei@dlut.edu.cn
Poly(hexamethylene succinate) copolyesters containing phosphorus pendent group: Retarded crystallization and solid-state microstructure
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论文类型:期刊论文
发表时间:2015-08-05
发表刊物:POLYMER
收录刊物:SCIE、EI、Scopus
卷号:71
页面范围:31-42
ISSN号:0032-3861
关键字:Poly(hexamethylene succinate); Retarded crystallization; Solid-state microstructure
摘要:Crystallization behavior and solid-state microstructure of poly(hexamethylene succinate) (PHS) and its phosphorus-containing copolyesters with bulky pendent group (DDP) have been investigated. The molecular weight, chemical structure and composition of the copolyesters were characterized and confirmed by GPC, H-1 and P-31 NMR. WAXD results suggest that the bulky DDP comonomer units in the copolyesters are noncrystallizable and are extruded from the crystal lattice of PHS. POM observations indicate that the spherulitic morphology becomes irregular and blurry with an increase of the DDP content. The kinetics analysis of isothermal crystallization shows that the crystallization of the copolyesters is retarded by the presence of the bulky DDP comonomer units. The observed crystallization and melting temperatures of the copolyesters are progressively depressed with the increase of DDP. SAXS quantitative analysis provides a proof that the significant increase in the long period of the copolyesters mainly arises from the increase in the amorphous layer, because the thickness of the lamellar increases slightly. A model of the lamellar crystal structure of the copolyester is proposed for its depression of the equilibrium melting temperature. (C) 2015 Elsevier Ltd. All rights reserved.