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Collective polyelectrolyte diffusion as a function of counterion size and dielectric constant
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SYSNO ASEP 0394493 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Článek ve WOS Title Collective polyelectrolyte diffusion as a function of counterion size and dielectric constant Author(s) Filippov, Sergey K. (UMCH-V) RID, ORCID, SAI
Seery, T. A. P. (US)
Kříž, Jaroslav (UMCH-V) RID
Hrubý, Martin (UMCH-V) RID, ORCID
Černoch, Peter (UMCH-V) RID, ORCID
Sedláček, Ondřej (UMCH-V) RID, ORCID
Kadlec, Petr (UMCH-V) RID, ORCID
Pánek, Jiří (UMCH-V) RID, ORCID
Štěpánek, Petr (UMCH-V) RID, ORCIDSource Title Polymer International. - : Wiley - ISSN 0959-8103
Roč. 62, č. 9 (2013), s. 1271-1276Number of pages 6 s. Language eng - English Country GB - United Kingdom Keywords polyelectrolyte ; counterion binding ; sodium polystyrene sulfonate Subject RIV CF - Physical ; Theoretical Chemistry R&D Projects ME09059 GA MŠMT - Ministry of Education, Youth and Sports (MEYS) CEZ AV0Z40500505 - UMCH-V (2005-2011) UT WOS 000322580300002 DOI 10.1002/pi.4410 Annotation We report studies of the effect of counterions on the properties of solutions of a strong polyelectrolyte for a wide range of solvent dielectric constant. For this purpose we investigated the dynamic properties of polystyrene sulfonate in N-methylformamide whose dielectric constant changes significantly with temperature. By means of dynamic light scattering and NMR spectroscopy, polymers of different molecular weights and various counterions were investigated, including large phosphazene counterions P1, P2 and P4 measured for the first time. It was found that the order of counterion binding of ionomers in the solvent changed with an increase of dielectric constant. The order for low dielectric constant (high temperature) was Na < Rb < Cs < P1 < P2 < P4, whereas for a solvent with high dielectric constant no influence of counterion nature was observed. The solvation–desolvation effect together with electrostatic interactions are responsible for the observed phenomenon. Workplace Institute of Macromolecular Chemistry Contact Eva Čechová, cechova@imc.cas.cz ; Tel.: 296 809 358 Year of Publishing 2014
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