Colloidal Systems in Concentrated Electrolyte Solutions Exhibit Re-entrant Long-Range Electrostatic Interactions due to Underscreening

被引:13
作者
Yuan, Haiyang [1 ]
Deng, Wenjie [1 ]
Zhu, Xiaolong [2 ]
Liu, Guangming [1 ]
Craig, Vincent Stuart James [1 ,3 ]
机构
[1] Univ Sci & Technol China, Dept Chem Phys, Key Lab Surface & Interface Chem & Energy Catalys, Hefei 230026, Peoples R China
[2] Univ Sci & Technol China, State Key Lab Fire Sci, Hefei 230026, Peoples R China
[3] Australian Natl Univ, Dept Appl Math, Res Sch Phys, Canberra, ACT 2601, Australia
基金
中国国家自然科学基金; 澳大利亚研究理事会;
关键词
SURFACE FORCE MEASUREMENTS; FOAM FILMS; WATER; LENGTH; DLVO; POLYELECTROLYTES; STABILITY; EMULSION; DRAINAGE; SILICA;
D O I
10.1021/acs.langmuir.2c00519
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Surface force measurements have revealed that at very high electrolyte concentrations as well as in neat and diluted ionic liquids and deep eutectic solvents, the range of electrostatic interactions is far greater than the Debye length. Here, we explore the consequences of this underscreening for soft-matter and colloidal systems by investigating the stability of nanoparticle dispersions, the self-assembly of ionic surfactants, and the thickness of soap films. In each case, we find clear evidence of re-entrant properties due to underscreening at high salt concentrations. Our results show that underscreening in concentrated electrolytes is a general phenomenon and is not dependent on confinement by macroscopic surfaces. The stability of systems at very high salinity due to underscreening may be beneficially applied to processes that currently use low-salinity water.
引用
收藏
页码:6164 / 6173
页数:10
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