Why does high pressure destroy co-non-solvency of PNIPAm in aqueous methanol?
Author:
Affiliation:
1. Max-Planck Institut für Polymerforschung
2. 55128 Mainz, Germany
3. Universidade Federal do Rio Grande do Sul
4. Porto Alegre, Brazil
Abstract
When a polymer collapses in a mixture of two competing good solvents, the phenomenon is termed as co-non-solvency that is driven by preferential adsorption of the better cosolvent with the polymer. High pressures, however, significantly reduce this preferential binding and thus destroy co-non-solvency of PNIPAm.
Publisher
Royal Society of Chemistry (RSC)
Subject
Condensed Matter Physics,General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2015/SM/C5SM01772F
Reference31 articles.
1. Cononsolvency in mixed aqueous solutions of poly(N-isopropylacrylamide)
2. Reentrant Coil-to-Globule-to-Coil Transition of a Single Linear Homopolymer Chain in a Water/Methanol Mixture
3. Molecular Dynamics and Experimental Study of Conformation Change of Poly(N-isopropylacrylamide) Hydrogels in Mixtures of Water and Methanol
4. Temperature dependent phase behavior of PNIPAM microgels in mixed water/methanol solvents
5. Temperature-Responsive Polymers in Mixed Solvents: Competitive Hydrogen Bonds Cause Cononsolvency
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