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Comparative dielectric studies of segmental and normal mode dynamics of poly(oxybutylene) and poly(oxyethylene)-poly(oxybutylene) diblock copolymers

机译:聚(氧银)和聚(氧乙烯)二嵌段共聚物(氧二乙烯)二嵌段(氧乙烯)二嵌段共聚物的分段和正常模式动力学的比较介电研究

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摘要

Diblock copolymers of ethylene oxide (E) and 1,2-butylene oxide (B), E/sub 30/B/sub n/, with a constant E-block length of 30 units and various B-block lengths (n=3-30), were investigated, in parallel with a series of homopoly(oxybutylene)s of similar B-block lengths, using broadband dielectric relaxation spectroscopy (10/sup -2/ 10/sup 9/ Hz). The normal mode relaxation process due to reorientation of the end-to-end vector, as well as the main (segmental) process caused by local chain motions, exhibited by the B-blocks in the copolymers and respectively by the homopoly(oxybutylene), were studied in comparison with each other. The Rouse model has been found to describe satisfactorily the molecular mobility of B/sub n/ blocks in the copolymers, whereas deviations from that model have been observed for the homopolymers. The results show that the B-blocks in the copolymers, constrained between lamellar crystals created by E-blocks, exhibit slower large scale motions.
机译:二嵌段共聚物的环氧乙烷(E)和1,2-丁基氧(B),E / Sub 30 / B / Sub N /,具有30个单位的恒定E嵌段长度和各种B嵌段长度(n = 3研究,与类似B嵌段长度的一系列均电(氧二丁烯)的一系列均电介电弛豫光谱(10 / sup -2 / 10 / sup 9 / Hz)平行进行研究。由于端到端向量的重新定位,以及由局部链运动引起的局部链运动引起的主要模式松弛过程,由共聚物中的B嵌段以及均多(氧二丁烯),与彼此相比研究过。已经发现rouse模型令人满意地描述共聚物中B / sub n /嵌段的分子迁移率,而已经从均聚物中观察到与该模型的偏差。结果表明,共聚物中的B嵌段约束在通过电子嵌段产生的层状晶体之间,表现出较慢的大规模运动。

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