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二维相关光谱在线跟踪聚(N-乙烯基己内酰胺)水凝胶的两步体积相变机制。

Two-step volume phase transition mechanism of poly(N-vinylcaprolactam) hydrogel online-tracked by two-dimensional correlation spectroscopy.

作者信息

Su Gehong, Zhou Tao, Liu Xifei, Zhang Yulin

机构信息

State Key Laboratory of Polymer Materials Engineering of China, Polymer Research Institute, Sichuan University, Chengdu 610065, China.

出版信息

Phys Chem Chem Phys. 2017 Oct 18;19(40):27221-27232. doi: 10.1039/c7cp04571a.

Abstract

In this study, temperature-dependent FTIR spectroscopy in combination with the perturbation-correlation moving-window (PCMW2D) technique and generalized two-dimensional (2D) correlation analysis was applied to investigate the phase transition mechanism of poly(N-vinylcaprolactam) (PVCL) hydrogel upon heating. In the conventional 1D FTIR spectra, the gradual dehydration of C-H groups, as well as the gradual dissociation of hydrogen bonds between C[double bond, length as m-dash]O groups and water molecules, was observed during phase transition. Moreover, we found that the rate at which water molecules were expelled out of the gel network during phase transition was changed to a sigmoid mode, rather than increasing linearly with increasing temperature. PCMW2D FTIR spectra revealed that the phase transition of PVCL hydrogel can be divided into two steps (named as I and II) upon heating, and we further determined the temperature regions of steps I and II to be 29.0-35.7 °C and 35.7-47.5 °C, respectively. Step I is the formation of hydrophobic domains in the gel, and step II is the chain collapse of the gel. Finally, with the help of generalized 2D correlation analysis, it was confirmed that the transformation of hydrogen bonds was the driving force of the hydrophobic domain formation process, while the hydrophobic interaction of C-H groups was the driving force for the chain collapse process. Combined with the obtained sequential orders of step I and step II, an integrated two-step phase transition mechanism of PVCL hydrogel upon heating was proposed.

摘要

在本研究中,将温度相关的傅里叶变换红外光谱(FTIR)与扰动相关移动窗口(PCMW2D)技术及广义二维(2D)相关分析相结合,用于研究聚(N - 乙烯基己内酰胺)(PVCL)水凝胶加热时的相变机制。在传统的一维FTIR光谱中,观察到在相变过程中C - H基团的逐渐脱水,以及C = O基团与水分子之间氢键的逐渐解离。此外,我们发现相变过程中水分子从凝胶网络中排出的速率转变为S形模式,而不是随温度升高呈线性增加。PCMW2D FTIR光谱显示,PVCL水凝胶加热时的相变可分为两个步骤(分别命名为I和II),我们进一步确定步骤I和步骤II的温度范围分别为29.0 - 35.7℃和35.7 - 47.5℃。步骤I是凝胶中疏水区域的形成,步骤II是凝胶的链塌陷。最后,借助广义二维相关分析,证实氢键的转变是疏水区域形成过程的驱动力,而C - H基团的疏水相互作用是链塌陷过程的驱动力。结合所获得的步骤I和步骤II的顺序,提出了PVCL水凝胶加热时的两步综合相变机制。

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