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首页> 外文期刊>Macromolecules >Anomalous swelling behavior of poly(N-vinylimidazole)-l- poly(tetrahydrofuran) amphiphilic conetwork in water studied by solid-state NMR and positron annihilation lifetime spectroscopy
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Anomalous swelling behavior of poly(N-vinylimidazole)-l- poly(tetrahydrofuran) amphiphilic conetwork in water studied by solid-state NMR and positron annihilation lifetime spectroscopy

机译:固态NMR和正电子lifetime没寿命谱研究聚(N-乙烯基咪唑)-1-聚(四氢呋喃)两亲共网络在水中的异常溶胀行为。

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摘要

Poly(N-vinylimidazole) homopolymer (PVIm) and poly(N-vinylimidazole)-l- poly(tetrahydrofuran) (PVIm-l-PTHF), a novel amphiphilic polymer conetwork (APCN), were synthesized to compare their solid state structure and investigate the swelling behavior of this unique conetwork in water. A short-range ordered structure stabilized by second-order interactions between the imidazole pendant groups was found in the PVIm homopolymer and in the PVIm phase of the dry conetwork as revealed by solid-state NMR ~(13)C cross-polarization magic angle spinning (CP MAS) and two-dimensional ~1H- ~(13)C frequency-switched Lee-Goldburg (FSLG) HETCOR measurements. With increasing swelling ratio, structural and conformational changes were recognized in the hydrophilic PVIm phase of the APCN. In the kinetic swelling study, unexpectedly, four different swelling ranges were identified by gravimetric measurements, solid-state NMR methods, and positron annihilation lifetime (PAL) spectroscopy before the APCN reached its equilibrium swelling state. In the first period, which takes place in several minutes, the ordered structure disintegrates in the PVIm phase and the water uptake is relatively slow. This structural realignment is followed by the main course of water uptake governed by Fickian diffusion in the second stage. Close to the equilibrium swelling ratio, the swelling curve becomes nonmonotonic caused by a realignment of main chains of the hydrophilic phase in the third stage of swelling. Thus, by the unique combination of conventional swelling kinetics and solid-state NMR as well as PAL spectroscopies for investigating the aqueous swelling of the PVIm-l-PTHF amphiphilic polymeric conetwork, it was revealed that unexpected noncontinuous swelling occurs which is due to structural changes of the PVIm component in the conetwork in the course of this process.
机译:合成了一种新型的两亲性聚合物共网络(APCN)聚(N-乙烯基咪唑)均聚物(PVIm)和聚(N-乙烯基咪唑)-1-聚四氢呋喃(PVIm-1-PTHF),以比较它们的固态结构和研究这种独特的网络在水中的溶胀行为。固态NMR〜(13)C交叉极化幻角纺丝法显示,在PVIm均聚物和干共网络的PVIm相中发现了由咪唑侧基之间的二级相互作用稳定的短程有序结构。 (CP MAS)和二维〜1H〜〜(13)C频率切换Lee-Goldburg(FSLG)HETCOR测量。随着溶胀率的增加,在APCN的亲水性PVIm相中识别出结构和构象变化。在动力学溶胀研究中,出乎意料的是,在APCN达到平衡溶胀状态之前,通过重量测量,固态NMR方法和正电子an没寿命(PAL)光谱法确定了四个不同的溶胀范围。在几分钟内的第一阶段中,有序结构在PVIm相中分解,吸水速度相对较慢。在结构调整之后,第二阶段受Fickian扩散控制的主要吸水过程。接近平衡溶胀率,溶胀曲线变得非单调,这是由溶胀第三阶段中亲水相的主链重新排列引起的。因此,通过常规溶胀动力学和固态NMR以及PAL光谱学的独特组合,用于研究PVIm-1-PTHF两亲聚合物共网络的水溶胀,发现由于结构变化而发生了意外的非连续溶胀在此过程中,PVIm组件在协同网络中的作用。

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