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聚N-异丙基丙烯酰胺在溶剂化机制转变时的共非溶剂化作用

Co-nonsolvency of PNiPAM at the transition between solvation mechanisms.

作者信息

Bischofberger I, Calzolari D C E, Trappe V

机构信息

University of Fribourg, Department of Physics, CH-1700 Fribourg, Switzerland.

出版信息

Soft Matter. 2014 Nov 7;10(41):8288-95. doi: 10.1039/c4sm01345j. Epub 2014 Sep 5.

Abstract

We investigate the co-nonsolvency of poly-N-isopropyl acrylamide (PNiPAM) in different water-alcohol mixtures and show that this phenomenon is due to two distinct solvation contributions governing the phase behavior of PNiPAM in the water-rich and alcohol-rich regime respectively. While hydrophobic hydration is the predominant contribution governing the phase behavior of PNiPAM in the water-rich regime, the mixing contributions governing the phase behavior of classical polymer solutions determine the phase behavior of PNiPAM in the alcohol-rich regime. This is evidenced by distinct scaling relations denoting the energetic state of the aqueous medium as a key parameter for the phase behavior of PNiPAM in the water-rich regime, while the volume fractions of respectively water, alcohol and PNiPAM become relevant parameters in the alcohol-rich regime. Adding alcohol to water decreases the energetics of the aqueous medium, which gradually suppresses hydrophobic hydration, while adding water to alcohol decreases the solvent quality. Consequently, PNiPAM is insoluble in the intermediate range of solvent composition, where neither hydrophobic hydration nor the mixing contributions prevail. This accounts for the co-nonsolvency phenomenon observed for PNiPAM in water-alcohol mixtures.

摘要

我们研究了聚-N-异丙基丙烯酰胺(PNiPAM)在不同水-醇混合物中的共非溶剂化现象,并表明这种现象是由于两种不同的溶剂化作用分别控制了PNiPAM在富水和富醇体系中的相行为。在富水体系中,疏水水合作用是控制PNiPAM相行为的主要因素,而在富醇体系中,控制经典聚合物溶液相行为的混合作用决定了PNiPAM的相行为。这通过不同的标度关系得到证明,在富水体系中,这些关系将水相介质的能量状态表示为PNiPAM相行为的关键参数,而在富醇体系中,水、醇和PNiPAM的体积分数则成为相关参数。向水中添加醇会降低水相介质的能量,这会逐渐抑制疏水水合作用,而向醇中添加水会降低溶剂质量。因此,PNiPAM在溶剂组成的中间范围内不溶,在该范围内,疏水水合作用和混合作用都不起主导作用。这就解释了在水-醇混合物中观察到的PNiPAM的共非溶剂化现象。

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