Synthesis and characterization of the PTMG aliphatic hyperbranched polyurethane

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作者
Key Laboratory of Chemistry and Technology for Light Chemical Industry, Ministry of Education, Shaanxi University of Science and Technology, Xi'an 710021, China [1 ]
机构
[1] Wang, Xue-Chuan
[2] Fu, Yu-Qiao
[3] Ren, Long-Fang
[4] Qiang, Tao-Tao
[5] Ren, Jing
来源
Fu, Y.-Q. | 1600年 / Journal of Functional Materials, P.O. Box 1512, Chongqing, 630700, China卷 / 44期
关键词
Dibutyltin dilaurate - Graft co polymerizations - Hyperbranched - Hyperbranched polyurethane - Isophorone disocyanate - Polyurethane prepolymers - Reaction conditions - Reaction temperature - Single-factor experiments - Step-growth polymerizations - Synthesis and characterizations;
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摘要
The isocyanate-terminated polyurethane prepolymer (PPU) was synthesized by step-growth polymerization using polytetramethylene ether glycol (PTMG, Mn=2000) with isophorone disocyanate (IPDI) as the monomers, dibutyltin dilaurate (DBTDL) as the catalyst. The appropriate reaction conditions were optimized by single factor experiments as follows. The reaction temperature was 75°C, the reaction time was 1.5 h and the quantity of catalyst was equal to 0.007% of feedstocks. And then the hyperbranched polyurethane (HBPU) was synthesized by graft copolymerization using isocyanate-terminated polyurethane prepolymer (PPU) and hyperbranched poly (amide-ester) polyol (HPAE) as the raw materials. The appropriate reaction conditions were optimized by single factor experiments as follows. The reaction temperature was 75°C, the reaction time was 4.5 h. The molecular structure of the monomers of PPU and HBPU were characterized by FT-IR. The thermal stability of PPU and HBPU were characterized by thermogravimetry.
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