魏志勇

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

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Synthesis and crystallization behavior of novel poly(butylene succinate) copolyesters containing phosphorus pendent groups

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论文类型:期刊论文

发表时间:2015-06-01

发表刊物:JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY

收录刊物:SCIE、EI、Scopus

卷号:120

期号:3

页面范围:1799-1810

ISSN号:1388-6150

关键字:Poly(butylene succinate); Crystallization; Melting behavior; Phosphorus containing

摘要:Novel biodegradable poly(butylene succinate) (PBS) copolyesters containing phosphors flame-retardant groups were synthesized by melt-polycondensation from succinic acid and 9,10-dihydro-10-[2,3-di(hydroxycarbonyl)propyl]-10-phosphaphenanthrene-10-oxide (DDP) with 1,4-butanediol. In order to analyze the effects of the third monomer (DDP) on the relative properties of PBS, the composition, crystal structure, crystallization behavior, multiple melting behavior, and spherulitic morphology of the copolyesters were investigated by H-1-NMR, WAXD, DSC, and POM, respectively. WAXD data revealed that the crystal structure of PBS was not affected by DDP. The overall crystallization kinetic showed that the crystallization of PBS was retarded with the introduction of DDP, especially when the DDP content exceeds 7.5 mol%, which may result from the stereo-hindrance of DDP unit. Furthermore, crystallization temperature (T (c)), crystallization enthalpy (Delta H (c)), melting temperature (T (m)), and crystallinity (X (c)) of PBS copolyesters also decreased apparently with the increase in DDP contents. Also, the equilibrium melting temperature (T (m) (o) ) obtained from Hoffman-Weeks analysis decreased, indicating that the regularity of PBS chain segments was reduced probably due to the diluent effect of the specific chain structure of DDP. All spherulites showed the ring-banded extinction patterns, which implied that phosphorus-containing (DDP) segment did not change the growth mechanism of PBS crystals.