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纸质出版日期:1964-2-20,
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刘有成, 伍宣池, 赵长义, 陈伟, 姚安亚, 高慧秀. 苯乙炔聚合反应的研究[J]. 高分子学报, 1964,6(1):71-77.
Liu Yu-cheng, WU SHUAN-CHIH, CHAO CHONG-YI, CHEN WEI, YAO AN-YA, KAO HWEI-SHIU. STUDIES ON THE POLYMERIZATION OF PHENYLACETYLENE[J]. Acta Polymerica Sinica, 1964,6(1):71-77.
研究了用苯甲酰过氧化物作引发剂的苯乙炔的聚合作用。当引发剂的用量为单体的1克分子%以下时
在60°
聚合作用很少进行
当引发剂的用量为2—4克分子%时
聚合作用明显地发生。当温度由60°升高到130°时
聚合速度显著地增加。所得聚合物的平均分子量为600—1500。红外光谱显示聚合物分子中有C6H5COO—端基的存在。在160°聚合产物的红外光谱中
C=O和C—O键的特征吸收基本上消失。 苯乙炔的热聚合在100°以下很少发生
在100—160°
聚合速度随温度升高而迅速增加。 三氟化硼不论在室温或较低温度可以引起苯乙炔的急骤聚合
所得聚苯乙炔的平均分子量在2000以上。 测定了几种聚苯乙炔样品的红外光谱
其中除引发聚合产物显示的苯甲酰氧基的C=O与C—O键的特征吸收外
其余均颇类似。与Okamoto等报导的聚苯乙炔的红外光谱相比较
只是在770—700厘米~(-1)区域内有微小的差异
而光谱的绝大部分是十分类似。因此可以认为
本文中报导的用几种不同的方法所得到的聚苯乙炔很可能具有相同的键结构:
The benzoyl peroxide-induced polymerization of phenylacetylene has been studied.At 60°.when the amount of the initiator used was less than 1 mole per cent of the monomer,very little polymerization occurred;when 2—4 mole per cent of the initiator was used,polymerization took place readily. When the temperature of polymerization was raised from 60°to 130°,the rate of polymerization increased markedly.The average molecular weight of the polyphenylacetylenes obtained was 600—1500.The in-frared spectrum of the polymer showed characteristic absorption for the C6H5COO-ter-minal group.In the infrared spectrum of the polymer obtained at 160°,the charac-teristic absorption peaks for the C=O and C—O bonds essentially vanished.The thermal polymerization of phenylacetylene occurred to a negligible extent be-low 100°;at 100—160°,the rate of polymerization、increased with increasing tempera-ture.Boron trifluoride could induce the rapid polymerization of phenylacetylene whether at room temperature or lower.The average molecular weight of the polyphenylacetylene obtained was over 2000.The infrared spectra of the polyphenylacetylenes showed great similarities,except the characteristic absorption for the C6H5COO-grouping in the benzoyl peroxide-initiated polymerization product.In comparison with the infrared spectrum of polyphenylace-tylene reported bv Okamoto et al[6] there was a minor difference in the 770—700 cm-1 region,while most parts of the spectra are very much similar;this indicates that the poly-phenylacetylenes obtained by the various methods reported in this work have probably the same chain structure.
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