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作 者:柏海见[1] 邓春华[1] 易建军[1] 陈继明[1] 齐永新[1] 潘广勤[1]
机构地区:[1]中国石油兰州石化公司研究院,兰州730060
出 处:《合成橡胶工业》2013年第3期172-175,共4页China Synthetic Rubber Industry
摘 要:以硅烷保护羟基的烷基锂为引发剂,采用负离子聚合法合成了端羟基聚丁二烯(HTPB),通过核磁共振氢谱、傅里叶变换红外光谱、凝胶渗透色谱和差示扫描量热法表征了HTPB的微观结构、分子量分布、官能度及玻璃化转变温度(Tg),研究了HTPB胶片的拉伸性能,并与自由基法HTPB进行了对比。结果表明,负离子法HTPB的1,4-结构摩尔分数约为90%,比自由基法HTPB高约12%,分子量分布小于1.1,低于自由基法HTPB,平均官能度比自由基法HTPB更接近理想值2,Tg为-88.3℃,较自由基法HTPB低9.7℃;负离子法HTPB胶片的拉伸强度与自由基法HTPB胶片相近,但扯断伸长率比自由基法HTPB胶片提高约74%。Hydroxyl-terminated polybutadiene ( HTPB ) was synthesized via anionic polymerization using silane-protected hy-droxyl alkyllithium as initiator, the microstructures, molecular-weight distribution, functionality and glass-transition temperature (T) were characterized by Fourier transform infrared spectros-copy, ^1H-nuclear magnetic resonance, gel permeation chroma- tography and differential scanning calorimetry, the tensile prop-erty of HTPB films was studied, and compared with those of free radical HTPB. The results showed that the mole fraction of 1,4-unit in anionic HTPB reached 90% or so, 12% more than that in free radical HTPB, the molecular weight distribution (less than 1.1 ) was lower than that of the latter, the functionality was more closer to ideal value of 2 than that of the latter, Tg was about - 88.3 ℃, 9. 7 ℃ less than that of latter. The tensile strength of anionic HTPB film was close to that of free radical HTPB film, but the elongation at break increased by 74%.
关 键 词:负离子聚合法 自由基聚合法 端羟基聚丁二烯 微观结构 分子量分布 官能度 玻璃化转变温度 拉伸性能
分 类 号:TQ316.324[化学工程—高聚物工业]
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