Insertion of anionic synthetic clay in lamellar surfactant phases

IF 1.8 4区 物理与天体物理 Q4 CHEMISTRY, PHYSICAL
Isabelle Grillo, Sylvain Prévost, Thomas Zemb
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Abstract

We describe the different mixed colloidal solutions that can be obtained when mixing equivalent quantities of a synthetic anionic clay to surfactants forming lamellar phases in the absence of added salt. The important quantity driving toward insertion or depletion is the osmotic pressure, of the lamellar phase and of the clay alone. Competition for water is the main driving force toward dispersion, inclusion or exclusion (phase separation). In the case of a nonionic surfactant (\(\hbox {C}_{12}\hbox {E}_{5}\)) mixed with Laponite, undulations quenched by the surfactant-decorated clay lead to swelling; inclusion is not observed due to differences in rigidity. Long-range order is weakened leading eventually to the exclusion of surfactant in excess. In the case of a double anionic system (AOT-Laponite), electrostatic is dominant and the three regimes are encountered. In the catanionic case, admixing the double chain cationic lipid DDAB to the clay (in large charge excess), the platelets are coated by a positively charged bilayer. Long-range order is very efficiently dampened. From a low threshold (2% by weight), there is exclusion of a clay-poor collapsed lamellar phase, detected by the swelling of the main phase. The cationized clay does not interfere with the molecular force balance: the location of the critical point is unchanged. At high Laponite concentration, a very puzzling microstructure is observed. Some phase diagrams as well as representative SANS and SAXS data are extracted from the complete results concerning the lyotropic lamellar phase mixing problem available with all measures and evaluations of osmotic pressures in the PhD of the late Isabelle Grillo.

Binary surfactant–water systems often form lamellar phases with spacing and osmotic pressure imposed by molecular interactions, while clay forms sols, gels and flocs with smectic order. The question addressed here is: “which mechanism is dominant in the center of the ternary phase diagram?”

Abstract Image

Abstract Image

片状表面活性剂相中阴离子合成粘土的插入
摘要 我们描述了在不添加盐的情况下,将等量的合成阴离子粘土与形成片层相的表面活性剂混合后可获得的不同混合胶体溶液。片层相和粘土本身的渗透压是驱动插入或耗尽的重要因素。对水的竞争是导致分散、包容或排斥(相分离)的主要动力。在非离子表面活性剂(\(\hbox {C}_{12}\hbox {E}_{5}/))与皂石混合的情况下,表面活性剂装饰的粘土所淬灭的起伏会导致膨胀;由于刚度不同,不会观察到包含。长程有序性被削弱,最终导致表面活性剂过量被排除。在双阴离子体系(AOT-皂石)中,静电占主导地位,并出现了三种状态。在阴离子情况下,将双链阳离子脂质 DDAB 混合到粘土中(电荷过量),血小板会被带正电荷的双电层包覆。长程秩序被有效抑制。从较低的阈值(2%(重量))开始,就会出现贫粘土塌陷片层相,并通过主相的膨胀来检测。阳离子化粘土不会干扰分子力平衡:临界点的位置保持不变。在皂石浓度较高的情况下,会观察到非常令人费解的微观结构。一些相图以及具有代表性的 SANS 和 SAXS 数据是从已故 Isabelle Grillo 博士关于各向同性片状相混合问题的完整结果中提取出来的,其中包含对渗透压的所有测量和评估。这里要解决的问题是"在三元相图的中心,哪种机制占主导地位?
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来源期刊
The European Physical Journal E
The European Physical Journal E CHEMISTRY, PHYSICAL-MATERIALS SCIENCE, MULTIDISCIPLINARY
CiteScore
2.60
自引率
5.60%
发文量
92
审稿时长
3 months
期刊介绍: EPJ E publishes papers describing advances in the understanding of physical aspects of Soft, Liquid and Living Systems. Soft matter is a generic term for a large group of condensed, often heterogeneous systems -- often also called complex fluids -- that display a large response to weak external perturbations and that possess properties governed by slow internal dynamics. Flowing matter refers to all systems that can actually flow, from simple to multiphase liquids, from foams to granular matter. Living matter concerns the new physics that emerges from novel insights into the properties and behaviours of living systems. Furthermore, it aims at developing new concepts and quantitative approaches for the study of biological phenomena. Approaches from soft matter physics and statistical physics play a key role in this research. The journal includes reports of experimental, computational and theoretical studies and appeals to the broad interdisciplinary communities including physics, chemistry, biology, mathematics and materials science.
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