Dynamic Mechanical Properties of a Polyelectrolyte Adsorbed Insoluble Lipid Monolayer at the Air-Water Interface

被引:1
|
作者
Park, Chang Young [1 ,2 ]
Kim, Mahn Won [1 ,2 ,3 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Phys, Taejon 305701, South Korea
[2] Univ Calif Santa Barbara, Mat Res Lab, Santa Barbara, CA 93106 USA
[3] Gwangju Inst Sci & Technol, Gwangju Coll, Gwangju 500712, South Korea
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2015年 / 119卷 / 16期
基金
新加坡国家研究基金会;
关键词
SODIUM POLY(STYRENESULFONATE); MEMBRANE; SURFACE; ADSORPTION; DRAG; PHASE; CELLS;
D O I
10.1021/jp5123773
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
Polymers have been used to stabilize interfaces or to tune the mechanical properties' of interfaces in various contexts, such oil emulsions or biological membranes. Although the structural properties of these systems are relatively well studied, instrumental limitations continue to make it difficult to understand how the addition of polymer affects the dynamic mechanical properties of thin and soft films. We have solved this challenge by developing a new instrument, an optical-tweezer-based interface shear micro-rheometer (ISMR). With this technique, we observed that the interface shear Modulus, G*, of a dioctadecyldimethyl-ammonium chloride-(DODAC) monolayer at the air-water interface significantly increased with adsorption of polystyrenesulfonate (PSS). In addition, the viscous film (DODAC monolayer) became a viscoelastic film with PSS adsorption. At a low salt concentration, 10 mM of NaCl in the subphase, the viscoelasticity of the DODAC/PSS composite was predominantly determined by a particular property of PSS, that is, it behaves as a Gaussian chain in a theta-solvent. At a high salt concentration, 316 mM of NaCl, the thin film behaved as a polymer melt excluding water molecules.
引用
收藏
页码:5315 / 5320
页数:6
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