Exploration of the unusual two-step volume phase transition of the poly(N-vinylcaprolactam-co-hydroxyethyl methacrylate) hydrogel

文献情報

出版日 2018-08-13
DOI 10.1039/C8CP02429D
インパクトファクター 3.676
著者

Gehong Su, Liyang Jia, Xueqian Zhang, Yulin Zhang, Pengchi Deng, Tao Zhou


原文を見る

要旨

It is important to investigate the phase transition mechanism of stimuli-sensitive hydrogels due to its great guiding significance for the application of stimuli-sensitive hydrogels in biomedical applications. In this work, the novel thermo-sensitive poly(N-vinylcaprolactam-co-hydroxyethyl methacrylate) (PVCL-co-HEMA) hydrogel was successfully synthesized via free radical polymerization, and then temperature-dependent FTIR spectra combined with the newly developed scaling moving-window two-dimensional (scaling-MW2D) correlation spectroscopy and generalized two-dimensional correlation analysis were utilized to investigate its volume phase transition (VPT) mechanism upon heating. Conventional 1D FTIR spectra and Boltzmann fitting results revealed that the PVCL-co-HEMA hydrogel exhibited a distinct VPT behavior from the neat PVCL hydrogel due to the incorporation of PHEMA. The essential reason is that some water molecules were still confined in the PVCL-co-HEMA network after phase transition at high temperature, rather than continuously being expelled out of the gel with the increase of temperature. Scaling-MW2D spectra revealed that the phase transition of the PVCL-co-HEMA hydrogel could be divided into two steps (I and II), and further confirmed that the transition regions of these two steps were 25.0–32.3 °C and 32.3–46.8 °C, respectively. The transition regions of both these steps were obviously lower than those of the neat PVCL hydrogel. According to the generalized 2D correlation analysis of step I, we concluded that the dissociation of the hydrogen bonds between the incorporated PHEMA moieties and water molecules is the driving force for the local hydrophobic domain formation process (step I), and its occurrence at a lower temperature is the main reason for the decrease of the VPTT of the PVCL segments. Furthermore, we found that the dissociation of the hydrogen bonds between the COVCL groups and water molecules is the driving force for the chain collapse (step II), and the driving effect of the PVCL segments on PHEMA during the phase transition was confirmed. Combined with the obtained sequential order of steps I and II, an unusual two-step VPT mechanism for the PVCL-co-HEMA hydrogel upon heating was proposed.

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Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics
CiteScore: 5.5
自己引用率: 10.3%
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Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.

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