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Copolymerizations of carbon dioxide and Epoxides in the presence of rare earth coordinate catalyst

机译:稀土配位催化剂存在下二氧化碳和环氧化物的共聚

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摘要

Carbon dioxide (CO2) as a direct material was copolymerized with epoxides to synthesize new aliphatic polycarbonates, and the copolymerization was catalyzed by the coordinate catalyst composed of rare earth yttrium phosphonate and triisobutylaluminum [Y(P-204)3(-)Al(i-Bu)(3)]. The epoxides used in this research included epichlorohydrin (ECH) and some new glycidol ether (GE) monomers prepared by the reaction of ECH and phenol or alcohol, such as a-allyl glycidol ether, beta-chloroethyl glycidol ether, benzene glycidol ether, m-tolyl glycidol ether, and benzyl glycidol ether. The copolymers were characterized by infrared (IR), H-1 nuclear magnetic resonance (-NMR), and dynamic mechanical analysis. The results show that Y(P-204)(3)-A1(i-Bu)(3) had better catalytic activity in the copolymerization of CO2 with epoxide, and the copolymerization rate of aryl GE was distinctly higher than that of aliphatic GE. Dynamic mechanical analysis indicated the glass transition temperature T of the copolymers GE-CO2 were lower than that of ECH-CO2. (C) 2003 Wiley Periodicals, Inc. J Appl Polym Sci 87: 2356 -2359, 2003. [References: 17]
机译:将二氧化碳(CO2)作为直接材料与环氧化物共聚以合成新型脂肪族聚碳酸酯,并通过稀土膦酸钇钇与三异丁基铝[Y(P-204)3(-)Al(i)组成的配位催化剂催化共聚。 -Bu)(3)]。该研究中使用的环氧化物包括环氧氯丙烷(ECH)和一些通过ECH与酚或醇反应制备的新缩水甘油醚(GE)单体,例如α-烯丙基缩水甘油醚,β-氯乙基缩水甘油醚,苯缩水甘油醚, -甲苯基缩水甘油醚和苄基缩水甘油醚。通过红外(IR),H-1核磁共振(-NMR)和动态力学分析对共聚物进行表征。结果表明,Y(P-204)(3)-A1(i-Bu)(3)在CO2与环氧化物的共聚中具有更好的催化活性,芳基GE的共聚速率明显高于脂族GE 。动态力学分析表明,共聚物GE-CO2的玻璃化转变温度T低于ECH-CO2。 (C)2003 Wiley Periodicals,Inc. J Appl Polym Sci 87:2356 -2359,2003. [参考文献:17]

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