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基于聚[2-(2-甲氧基乙氧基)乙基甲基丙烯酸酯]的温敏水凝胶的溶胀诱导各向异性:定量 Mueller 矩阵偏振法研究溶胀动力学。

Swelling-induced optical anisotropy of thermoresponsive hydrogels based on poly(2-(2-methoxyethoxy)ethyl methacrylate): deswelling kinetics probed by quantitative Mueller matrix polarimetry.

机构信息

Polymer Research Centre, Department of Chemical Sciences, Indian Institute of Science Education and Research, Kolkata, PO: BCKV Campus Main Office, Mohanpur-741252, Nadia, West Bengal, India.

出版信息

J Phys Chem B. 2012 Nov 29;116(47):13913-21. doi: 10.1021/jp308850a. Epub 2012 Nov 15.

DOI:10.1021/jp308850a
PMID:23131002
Abstract

Thermodynamically favored polymer-water interactions below the lower critical solution temperature (LCST) caused swelling-induced optical anisotropy (linear retardance) of thermoresponsive hydrogels based on poly(2-(2-methoxyethoxy)ethyl methacrylate). This was exploited to study the macroscopic deswelling kinetics quantitatively by a generalized polarimetry analysis method, based on measurement of the Mueller matrix and its subsequent inverse analysis via the polar decomposition approach. The derived medium polarization parameters, namely, linear retardance (δ), diattenuation (d), and depolarization coefficient (Δ), of the hydrogels showed interesting differences between the gels prepared by conventional free radical polymerization (FRP) and reversible addition-fragmentation chain transfer polymerization (RAFT) and also between dry and swollen state. The effect of temperature, cross-linking density, and polymerization technique employed to synthesize hydrogel on deswelling kinetics was systematically studied via conventional gravimetry and corroborated further with the corresponding Mueller matrix derived quantitative polarimetry characteristics (δ, d, and Δ). The RAFT gels exhibited higher swelling ratio and swelling-induced optical anisotropy compared to FRP gels and also deswelled faster at 30 °C. On the contrary, at 45 °C, deswelling was significantly retarded for the RAFT gels due to formation of a skin layer, which was confirmed and quantified via the enhanced diattenuation and depolarization parameters.

摘要

低于低临界溶解温度 (LCST) 的热力学有利的聚合物-水相互作用导致基于聚[2-(2-甲氧基乙氧基)乙基甲基丙烯酸酯]的温敏水凝胶的溶胀诱导光学各向异性(线性延迟)。利用这一性质,通过广义偏振分析方法,基于 Mueller 矩阵的测量及其通过偏振分解方法的逆分析,定量研究了宏观退溶动力学。水凝胶的衍生介质偏振参数,即线性延迟(δ)、消光(d)和去偏振系数(Δ),在通过传统自由基聚合(FRP)和可逆加成-断裂链转移聚合(RAFT)制备的凝胶之间以及在干燥和溶胀状态之间显示出有趣的差异。通过传统的重量分析法系统地研究了温度、交联密度和用于合成水凝胶的聚合技术对退溶动力学的影响,并通过相应的 Mueller 矩阵推导的定量偏振特性(δ、d 和 Δ)进一步证实。与 FRP 凝胶相比,RAFT 凝胶表现出更高的溶胀比和溶胀诱导的光学各向异性,并且在 30°C 下退溶更快。相反,在 45°C 下,由于形成了表皮层,RAFT 凝胶的退溶明显受到阻碍,这通过增强的消光和去偏振参数得到了证实和量化。

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