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首页> 外文期刊>Polymer: The International Journal for the Science and Technology of Polymers >Solid-state ~(19)F MAS and ~1H->~(19)F CP/MAS NMR study of the phase transition behavior of vinylidene fluoride-trifluoroethylene copolymers:1.Uniaxially drawn films of VDF 75% copolymer
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Solid-state ~(19)F MAS and ~1H->~(19)F CP/MAS NMR study of the phase transition behavior of vinylidene fluoride-trifluoroethylene copolymers:1.Uniaxially drawn films of VDF 75% copolymer

机译:偏二氟乙烯-三氟乙烯共聚物的相变行为的固态〜(19)F MAS和〜1H->〜(19)F CP / MAS NMR研究:1.VDF 75%共聚物的单轴拉伸薄膜

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The changes in the phase structures and molecular mobility caused by the ferroelectric-paraelectric phase transition of vinylidene fluoride (VDF) and trifluoroethylene (TrFE) copolymer,P(VDF_(75)/TrFE_(25),were analyzed using variable temperature (VT) solid-state ~(19)F MAS and ~1H->~(19)F CP/MAS NMR spectroscopy.The CF_2 signal of the VDF chain sequence and the CHF signal at the head-to-head linkage of VDF-TrFE sequence showed higher frequency shift in the temperature range 43-92 deg C,whereas no change was found for the CHF signal at the head-to-tail linkage of VDF-TrFE up to 92 deg C.Hence,VT ~(19)F MAS spectra revealed that the VDF-TrFE head-to-tail sequence is the most stable part in polymer chains against trans-gauche conformational exchange motions below the phase transition temperature (Curie temperature,T_c) on heating.However,all chain sequences including TrFE units undergo conformational exchange at around T_c.The phase transition behavior is clearly recognized in the ~(19)F spectral shapes,in which the broad signals of the ferroelectric immobile phase disappeared between 115 and 119 deg C.In addition,T_(1rho)~F for all peaks decreased to a unique value (ca.20 ms) at 119 deg C,indicating that uniform molecular motion accompanied by a full chain rotation occurred at the temperature.The significantly longer T_(1rho)~T for all peaks (ca.20 ms) in the paraelectric phase (119 deg C) than that in the amorphous domain (<4 ms) at ambient temperature supports the conclusion that there is restricted rotational motion of polymer chains around the chain axis in the paraelectric phase.On cooling from 119 to 85 deg C,a gradual decrease in gauche conformers in the paraelectric phase was confirmed by the low-frequency displacement of CF_2 signals in VDF sequences accomopanied by slight decreases in T_1~F and T_(1rho)~F.The phase transition was observed between 85 and 77 deg C on cooling,in which the characteristic signals of the paraelectric phase disappeared,the T_(1rho)~F values of all peaks quickly increased,and the broad crystalline signals abruptly appeared at 77 deg C.
机译:使用可变温度(VT)分析了偏二氟乙烯(VDF)和三氟乙烯(TrFE)共聚物P(VDF_(75)/ TrFE_(25)的铁电-顺电相变引起的相结构和分子迁移率的变化固态〜(19)F MAS和〜1H->〜(19)F CP / MAS NMR光谱.VDF链序列的CF_2信号和VDF-TrFE序列的头对头连接处的CHF信号在43-92摄氏度的温度范围内显示出较高的频移,而在高达92摄氏度的VDF-TrFE的头尾连接处的CHF信号未发现变化。因此,VT〜(19)F MAS光谱显示,VDF-TrFE从头到尾序列是聚合物链中在加热时低于相变温度(居里温度,T_c)以下的反反态构象交换运动中最稳定的部分。在T_c附近进行构象交换。在((19)F)中明确识别出相变行为谱形状,其中铁电固定相的宽信号在115至119摄氏度之间消失。此外,所有峰的T_(1rho)〜F在119摄氏度下降至唯一值(约20毫秒),表明顺电相(119℃)下所有峰(约20 ms)的T_(1rho)〜T明显长于非晶区(<在室温下4毫秒)支持以下结论:顺电相中聚合物链绕链轴的旋转受到限制。从119冷却到85摄氏度时,顺电相中的gauche构象异构体逐渐减少,这证实了T_1〜F和T_(1rho)〜F略微减小,VDF序列中CF_2信号的低频位移。冷却时在85至77摄氏度之间观察到相变,顺电相的特征信号消失了,T_(1rho所有峰的)〜F值迅速增加,并在77℃突然出现宽晶体信号。

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