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作 者:王松松[1] 周大鹏[2] 谷俐[2] 李坚[1] 俞立琼
机构地区:[1]常州大学材料科学与工程学院,江苏常州213164 [2]嘉兴学院生物与化工学院,浙江嘉兴314033 [3]浙江嘉民塑胶有限公司,浙江嘉兴314027
出 处:《中国塑料》2011年第6期34-37,共4页China Plastics
摘 要:以三羟基丙烷和二羟甲基丙酸为原料,缩聚反应制备了超支化聚酯(HBPE),并制备了酚醛树脂/HBPE(PF/HBPE)共混体系。采用红外光谱、差示扫描量热分析等方法表征了HBPE的分子结构和PF/HBPE共混体系的性能,并用非模型等转化率法Flynn-Wall-Ozawa(FWO)描述了PF/HBPE共混体系的活化能与转化率之间的关系。结果表明,由于PF的酚羟基和HBPE的羟基产生了氢键作用,PF/HBPE共混体系显示出单一的玻璃化转变温度,HBPE的加入,提高了PF固化物的冲击强度和弯曲强度,当HBPE的含量为15%时,冲击强度和弯曲强度分别为4.5 kJ/m2和77.84 MPa。Hyperbranched polyester (HBPE) was synthesized via condensation polymerization of tri- ethytolpropane and 2, 2-is(hydroxymethyl) propionic acid, which was used to modify phenolic resins(PF). The structure and thermal property of the blend were characterized with FTIR and differential scanning calorimetry (DSC), a relation between the effective activation energy and the fractional conversion during the curing was determined using a model-free isoconversional method, viz, Flynn-Wall-Ozawa (FWO) method. Due to intermolecular hydrogen bonding between hydroxyl groups of HBPE and PF, a single glass transition was Observed. The impact and bend strengths of PF were increased with the addition of HBPE, reached 4. 5 kl/m^2 and 77.84 MPa. respectively.
分 类 号:TQ323.1[化学工程—合成树脂塑料工业]
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