首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Network Formation of Catanionic Vesicles and Oppositely Charged Polyelectrolytes.Effect of Polymer Charge Density and Hydrophobic Modification
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Network Formation of Catanionic Vesicles and Oppositely Charged Polyelectrolytes.Effect of Polymer Charge Density and Hydrophobic Modification

机译:阳离子囊泡和带正电的聚电解质的网络形成。聚合物电荷密度和疏水改性的影响

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In nonequimolar solutions of a cationic and an anionic surfactant,vesicles bearing a net charge can be spontaneously formed and apparently exist as thermodynamically stable aggregates.These vesicles can associate strongly with polymers in solution by means of hydrophobic and/or electrostatic interactions.In the current work,we háve investigated the rheological and microstructural properties of mixtures of cationic polyelectrolytes and net anionic sodium dodecyl sulfate/didodecyldimethylammonium bromide vesicles.The polyelectrolytes consist of two cationic cellulose derivatives with different charge densities; the lowest charge density polymer contains also hydrophobic grafts,with the number of charges equal to the number of grafts.For both systems,polymer-vesicle association leads to a major increase in viscosity and to gel-like behavior,but the viscosity effects are more pronounced for the less charged,hydrophobically modified polymer.Evaluation of the frequency dependence of the storage and loss moduli for the two systems shows further differences in behavior: while the more long-lived cross-links occur for the more highly charged hydrophilic polymer,the number of cross-links is higher for the hydrophobically modified polymer.Microstructure studies by cryogenic transmission electron microscopy indicate that the two polymers affect the vesicle stability in different ways.With the hydrophobically modified polymer,the aggregates remain largely in the form of globular vesicles and faceted vesicles (polygon-shaped vesicles with largely planar regions).For the hydrophilic polycation,on the other hand,the surfactant aggregate structure is more extensively modified: first,the vesicles change from a globular to a faceted shape; second,there is opening of the bilayers leading to holey vesicles and ultimately to considerable vesicle disruption leading to planar bilayer,disklike aggregates.The faceted shape is tentatively attributed to a crystallization of the surfactant film in the vesicles.It is inferred that a hydrophobically modified polyion with relatively low charge density can better stabilize vesicles due to formation of molecularly mixed aggregates,while a hydrophilic polyion with relatively high charge density associates so strongly to the surfactant films,due to strong electrostatic interactions,that the vesicles are more perturbed and even disrupted.
机译:在阳离子和阴离子表面活性剂的非等摩尔溶液中,带有净电荷的囊泡可以自发形成,并且显然以热力学稳定的聚集体形式存在。这些囊泡可以通过疏水和/或静电相互作用与溶液中的聚合物强烈缔合。在工作中,我们研究了阳离子聚电解质和净阴离子十二烷基硫酸钠/十二烷基二甲基溴化铵囊泡的混合物的流变学和微观结构特性。聚电解质由两种电荷密度不同的阳离子纤维素衍生物组成。电荷密度最低的聚合物还包含疏水性接枝,电荷数量等于接枝数量。对于这两个系统,聚合物-囊泡缔合会导致粘度显着增加并呈现凝胶状行为,但粘度影响更大两个系统的储能和损耗模量的频率相关性评估显示出行为上的进一步差异:当电荷较高的亲水性聚合物发生寿命更长的交联时,疏水改性的聚合物的交联数更高。低温透射电子显微镜的微观结构研究表明,这两种聚合物以不同的方式影响囊泡的稳定性。疏水改性的聚合物,聚集体主要以球形囊泡的形式保留下来。刻面小泡(具有较大平面区域的多边形小泡)。对于亲水性聚阳离子,在其他地方另一方面,表面活性剂的聚集体结构得到了更广泛的修饰:首先,囊泡从球状变为多面形;其次,双层的开放导致多孔的小泡,最终导致大量的小泡破裂,导致平面的双层,盘状聚集体。多面的形状暂时归因于表面活性剂膜在小泡中的结晶。据推测,疏水改性的是电荷密度相对较低的聚离子由于形成了分子混合的聚集体,因此可以更好地稳定囊泡,而电荷密度相对较高的亲水性聚离子由于强烈的静电相互作用而与表面活性剂膜紧密结合,以至于囊泡更易受干扰甚至破坏。 。

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