Tuning the collapse transition of weakly charged polymers by ion-specific screening and adsorption

被引:21
|
作者
Chudoba, Richard [1 ,2 ,3 ]
Heyda, Jan [4 ]
Dzubiella, Joachim [2 ,3 ]
机构
[1] Humboldt Univ, Inst Phys, Newtonstr 15, D-12489 Berlin, Germany
[2] Albert Ludwigs Univ Freiburg, Phys Inst, Hermann Herder Str 3, D-79104 Freiburg, Germany
[3] Helmholtz Zentrum Berlin, Res Grp Simulat Energy Mat, Hahn Meitner Pl 1, D-14109 Berlin, Germany
[4] Univ Chem & Technol Prague, Dept Phys Chem, Tech 5, CZ-16628 Prague 6, Czech Republic
关键词
VOLUME PHASE-TRANSITION; COUNTERION-CONDENSATION; FLEXIBLE POLYELECTROLYTES; N-ISOPROPYLACRYLAMIDE; HOFMEISTER SERIES; THERMODYNAMIC DESCRIPTION; GLOBULE TRANSITION; THERMAL-BEHAVIOR; EXCLUDED-VOLUME; CHAIN-LENGTH;
D O I
10.1039/c8sm01646a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The experimentally observed swelling and collapse response of weakly charged polymers to the addition of specific salts displays quite convoluted behavior that is not easy to categorize. Here we use a minimalistic implicit-solvent/explicit-salt simulation model with a focus on ion-specific interactions between ions and a single weakly charged polyelectrolyte to qualitatively explain the observed effects. In particular, we demonstrate ion-specific screening and bridging effects cause collapse at low salt concentrations whereas the same strong ion-specific direct interactions drive re-entrant swelling at high concentrations. Consistently with experiments, a distinct salt concentration at which the salting-out power of anions inverts from the reverse to direct Hofmeister series is observed. At this so called isospheric point, the ion-specific effects vanish. Furthermore, with additional simplifying assumptions, an ion-specific mean-field model is developed for the collapse transition which quantitatively agrees with the simulations. Our work demonstrates the sensitivity of the structural behavior of charged polymers to the addition of specific salt beyond simple screening and shall be useful for further guidance of experiments.
引用
收藏
页码:9631 / 9642
页数:12
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