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聚(N-异丙基丙烯酰胺)微凝胶的溶胀动力学

Swelling kinetics of poly(N-isopropylacrylamide) minigels.

作者信息

Suárez Ivan J, Fernández-Nieves Alberto, Márquez Manuel

机构信息

Group of Complex Fluids Physics, Department of Applied Physics, University of Almeria, Almería 04120, Spain.

出版信息

J Phys Chem B. 2006 Dec 28;110(51):25729-33. doi: 10.1021/jp0643754.

Abstract

We synthesize poly(N-isopropylacrylamide) (PNIPAM) gels with different sizes in the micrometer scale by a slight variation of a recent emulsion polymerization method (ref 1). The procedure is different than that typically used for obtaining macroscopic PNIPAM hydrogels. The resultant minigel suspension is polydisperse thus allowing the swelling kinetics for different gel sizes to be studied; we do so at temperatures below the volume-transition temperature by wetting with water previously dried particles. The resultant swelling is followed by optical video microscopy. We find that the characteristic swelling time scales with the inverse of the particle dimension squared, in agreement with theoretical predictions (ref 2). The proportionality constant is the network diffusion coefficient D, which for the minigels under consideration appears to be in between that of PNIPAM macrogels and the self-diffusion coefficient of water.

摘要

我们通过对最近的乳液聚合法(参考文献1)稍作改动,合成了微米级不同尺寸的聚(N-异丙基丙烯酰胺)(PNIPAM)凝胶。该方法与通常用于制备宏观PNIPAM水凝胶的方法不同。所得的微凝胶悬浮液是多分散的,因此可以研究不同凝胶尺寸的溶胀动力学;我们通过用预先干燥的颗粒用水润湿,在低于体积转变温度的温度下进行研究。通过光学视频显微镜观察所得的溶胀情况。我们发现,特征溶胀时间与颗粒尺寸平方的倒数成比例,这与理论预测(参考文献2)一致。比例常数是网络扩散系数D,对于所考虑的微凝胶,它似乎介于PNIPAM大凝胶的扩散系数和水的自扩散系数之间。

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