Complex Coacervation of Polymerized Ionic Liquids in Non-aqueous Solvents

被引:11
|
作者
Lee, Minjung [1 ]
Perry, Sarah L. [2 ]
Hayward, Ryan C. [1 ,3 ]
机构
[1] Univ Massachusetts, Dept Polymer Sci & Engn, Amherst, MA 01003 USA
[2] Univ Massachusetts, Dept Chem Engn, Amherst, MA 01003 USA
[3] Univ Colorado, Dept Chem & Biol Engn, Boulder, CO 80309 USA
来源
ACS POLYMERS AU | 2021年 / 1卷 / 02期
关键词
polymerized ionic liquids; complex coacervates; low-dielectric-constant solvents; phase diagrams; PHASE-BEHAVIOR; POLY(IONIC LIQUID)S; AQUEOUS-SOLUTIONS; POLYELECTROLYTE; DRIVEN; ELECTROLYTES; TEMPERATURE; PROTEINS; WATER; SALT;
D O I
10.1021/acspolymersau.1c00017
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Oppositely charged polymerized ionic liquids (PILs) were used to form complex coacervates in two different organic solvents, 2,2,2-trifluoroethanol (TFE) and hexafluoro-2-propanol (HFIP), and the corresponding phase diagrams were constructed using UV-vis, NMR, and turbidity experiments. While previous studies on complex coacervates have focused almost exclusively on aqueous environments, the use of PILs in the current work enabled studies in solvents with substantially lower dielectric constants (27.0 for TFE, 16.7 for HFIP). The critical salt concentration required to induce complete miscibility was roughly 2-fold larger in HFIP compared with TFE, and two different PIL complexes, solidlike precipitates and liquidlike coacervates, were found in both systems. This study provides insight into the effects of low-dielectric-constant solvents on complex coacervation, which has not been widely studied because of the limited solubility of conventional polyelectrolytes in these media.
引用
收藏
页码:100 / 106
页数:7
相关论文
共 50 条