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首页> 外文期刊>Journal of Applied Polymer Science >Effective Promotion of Tetrahydrofuran Polymerization Initiated with Heteropolyacid
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Effective Promotion of Tetrahydrofuran Polymerization Initiated with Heteropolyacid

机译:有效促进杂多酸引发的四氢呋喃聚合

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摘要

Tetrahydrofuran was plymerized using the heteropolyacid H_3PW_12O_40 as the initiator and ethylene oxide as the promoter, which effectively increased the rate and conversion of the polymerization. Water and butylene glycol were used to control the molecular weight of the product in the range of 1000-3000. The polymer was found to be polyether glycol containing 10-22 mol % oxyethylene moieties with hydroxyl groups at both chain ends. The melting point was ~10 deg C lower compared to polytetramethylene ether glycol having the same molecular weight. The concentration of active species remained unchanged in the main period of the polymerization, indicating the absence of chain termination. The values of the chain propagation rate constant of tetrahydrofuran polymerization at 0 and 20deg C were found to be 3.78×10~(-3) and 1.98×10~(-2) L mol~(-1) s~(-1), respectivley, which are close to the rate constant of chain propagation of tetrahydrofuran on ionic active species.
机译:使用杂多酸H_3PW_12O_40作为引发剂和环氧乙烷作为促进剂来聚合四氢呋喃,这有效地提高了聚合速率和转化率。使用水和丁二醇将产物的分子量控制在1000-3000的范围内。发现该聚合物是在两个链末端均具有羟基的含有10-22mol%的氧化乙烯部分的聚醚二醇。与相同分子量的聚四亚甲基醚二醇相比,熔点低约10摄氏度。在聚合反应的主要阶段,活性物质的浓度保持不变,表明没有链终止。发现四氢呋喃聚合在0和20°C时的链增长速率常数值为3.78×10〜(-3)和1.98×10〜(-2)L mol〜(-1)s〜(-1) ,接近四氢呋喃在离子活性物质上链增长的速率常数。

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