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1.上海交通大学材料科学与工程学院 上海 200240
2.威海晨源分子新材料有限公司 威海 264211
3.上海交通大学化学化工学院 上海 200240
黄卫, E-mail:hw66@sjtu.edu.cn Huang Wei, E-mail:hw66@sjtu.edu.cn
纸质出版日期:2017-8,
收稿日期:2016-12-8,
修回日期:2016-12-27,
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汪羽翎, 李武松, 刘聪聪, 黄卫, 颜德岳, 康宏强. 超支化聚酯酰胺的合成及在聚碳酸酯加工中的应用[J]. 高分子学报, 2017,(8):1304-1311.
Wang Yu-ling, Li Wu-song, Liu Cong-cong, Huang Wei, Yan De-yue, Kang Hong-qiang. Synthesis of Hyperbranched Poly (ester amide) s and Their Application in Polycarbonate as Rheological Modification Agent[J]. Acta Polymerica Sinica, 2017,(8):1304-1311.
汪羽翎, 李武松, 刘聪聪, 黄卫, 颜德岳, 康宏强. 超支化聚酯酰胺的合成及在聚碳酸酯加工中的应用[J]. 高分子学报, 2017,(8):1304-1311. DOI: 10.11777/j.issn1000-3304.2017.16355.
Wang Yu-ling, Li Wu-song, Liu Cong-cong, Huang Wei, Yan De-yue, Kang Hong-qiang. Synthesis of Hyperbranched Poly (ester amide) s and Their Application in Polycarbonate as Rheological Modification Agent[J]. Acta Polymerica Sinica, 2017,(8):1304-1311. DOI: 10.11777/j.issn1000-3304.2017.16355.
以1,2,4-偏苯三羧酸酐(BTAA)和乙醇胺(EMA)为原料,分别采用"二步法"和"一步法"熔融缩聚制备了端羧基超支化聚酯酰胺(HBPEA).第1步利用官能团非等活性原理,在乙醇溶剂中由BTAA中高活性的酸酐基团与EMA中高活性的氨基反应原位生成含1个羟基和2个羧基的AB
2
中间体,蒸除乙醇后,再第2步熔融缩聚得到超支化聚酯酰胺,可避免聚合过程中发生凝胶.为便于工业化应用,还采用BTAA与EMA经"一步"熔融缩聚制备了端羧基超支化聚酯酰胺.分别采用核磁共振(NMR)、乌氏黏度计、示差扫描量热仪(DSC)、热失重分析仪(TGA)以及阿贝折射仪等对2种方法所制备的目标产物化学结构和特性黏度等各项性能进行了表征,结果表明:所得聚酯酰胺具有超支化结构,特性黏数为0.12~0.15 dL/g,支化度为0.64~0.65,在350℃之前未发生热失重,玻璃化转变温度为125~126℃,折射率为1.57~1.58,与聚碳酸酯(PC)相近.因此将其作为加工助剂用于PC塑料体系的加工.超支化聚酯酰胺的加入,不仅能改善PC的加工流动性,同时还能改善制品的机械性能和表面光洁度,且不会引起PC色泽的变化.
Due to highly branched three-dimensional sphere-like molecular architecture
hyperbranched polymers have shown very different properties such as intramolecular cavities
low viscosity
high solubility and a large number of terminal functional groups if compared with their linear analogues. They can be facilely synthesized
via
a one-pot polymerization through different methods according to the type of monomers
including polycondensation of AB
n
monomers
self-condensing vinyl polymerization
self-condensing ring-opening polymerization and so on. Here
hyperbranched poly(ester amide)s (HBPEAs) with terminal carboxyl groups are prepared from benzene-1
2
4-tricarbonylic acid-1
2-anhydride (BTAA) and ethanolamine (EMA)
via
two-step and one-step melt polycondensation
respectively. In two-step method
the anhydride group in BTAA first reacted with the amino group in EMA to form a AB
2
intermediate with one hydroxyl groups and two carboxyl groups in ethanol according to the principle of non-equal reactivity of functional groups. After ethanol evaporated
the AB
2
intermediate was melted at 220℃ to polymerize to produce HBPEA without gelation. Furthermore
HBPEA was also synthesized from BTAA and EMA at 220℃ through one-step melt polycondensation
more convenient in the industry. The resulting HBPEAs were characterized by
1
H-NMR analysis
Ubbelohde viscometer
differential scanning calorimeter (DSC)
thermo gravimetric analyzer (TGA) and refractive index measurements. their DBs are about 0.64 and intrinsic viscosities are about 0.120~0.146 dL/g. Their
T
g
s are about 125℃ and refraction indexes are about 1.57~1.58
which is similar to those of PC. The temperature of 5 wt% weight loss is above 350℃. Therefore
HBPEAs can be used as modification agent to process polycarbonate. When HBPEAs were added into PC or PC/CaCO
3
not only the process ability of PC or PC/CaCO
3
was improved
but also the colour of PC was kept unchanged. In addition
the mechanical properties and the surface roughness of PC or PC/CaCO
3
were enhanced too. In summary
HBPEAs have very broad prospects for different applications.
超支化聚酯酰胺熔融聚合加工助剂聚碳酸酯
Hyperbranched poly (ester amide)Melt polycondensationRheological modificationPolycarbonate
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