Ionic micelles and aromatic additives: a closer look at the molecular packing parameter

被引:31
|
作者
Lutz-Bueno, Viviane [1 ,2 ]
Isabettini, Stephane [1 ]
Walker, Franziska [1 ]
Kuster, Simon [1 ]
Liebi, Marianne [2 ,3 ]
Fischer, Peter [1 ]
机构
[1] Swiss Fed Inst Technol, Inst Food Nutr & Hlth, CH-8092 Zurich, Switzerland
[2] Paul Scherrer Inst, Swiss Light Source, CH-5232 Villigen, Switzerland
[3] Lund Univ, MAX Lab 6, S-22100 Lund, Sweden
关键词
SURFACTANT SOLUTIONS; RHEOLOGICAL BEHAVIOR; CATIONIC SURFACTANTS; DETERGENT MOLECULES; WORMLIKE MICELLES; CTAB SOLUTIONS; AQUEOUS-MEDIA; TRANSITION; SCATTERING;
D O I
10.1039/c7cp03891g
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
Wormlike micellar aggregates formed from the mixture of ionic surfactants with aromatic additives result in solutions with impressive viscoelastic properties. These properties are of high interest for numerous industrial applications and are often used as model systems for soft matter physics. However, robust and simple models for tailoring the viscoelastic response of the solution based on the molecular structure of the employed additive are required to fully exploit the potential of these systems. We address this shortcoming with a modified packing parameter based model, considering the additive-surfactant pair. The role of charge neutralization on anisotropic micellar growth was investigated with derivatives of sodium salicylate. The impact of the additives on the morphology of the micellar aggregates is explained from the molecular level to the macroscopic viscoelasticity. Changes in the micelle's volume, headgroup area and additive structure are explored to redefine the packing parameter. Uncharged additives penetrated deeper into the hydrophobic region of the micelle, whilst charged additives remained trapped in the polar region, as revealed by a combination of H-1-NMR, SAXS and rheological measurements. A deeper penetration of the additives densified the hydrophobic core of the micelle and induced anisotropic growth by increasing the effective volume of the additive-surfactant pair. This phenomenon largely influenced the viscosity of the solutions. Partially penetrating additives reduced the electrostatic repulsions between surfactant headgroups and neighboring micelles. The resulting increased network density governed the elasticity of the solutions. Considering a packing parameter composed of the additive-surfactant pair proved to be a facile means of engineering the viscoelastic response of surfactant solutions. The self-assembly of the wormlike micellar aggregates could be tailored to desired morphologies resulting in a specific and predictable rheological response.
引用
收藏
页码:21869 / 21877
页数:9
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