Ringdal N I, Fonseca D M, Hansen E L, Hemmen H, Fossum J O
Department of Physics, Norwegian University of Science and Technology, Hoegskoleringen 5, N-7491 Trondheim, Norway.
Phys Rev E Stat Nonlin Soft Matter Phys. 2010 Apr;81(4 Pt 1):041702. doi: 10.1103/PhysRevE.81.041702. Epub 2010 Apr 7.
We have studied stable strata of gravity-induced phase separation in suspensions of synthetic Na-fluorohectorite clay in saline solutions. We have observed how the strata depend on clay concentration as well as on salt content. The mass distribution and density variation at the isotropic-nematic interface indicate that existing models and assumptions in existing simulations are able to relatively well account for the observed behavior. We suggest that discrepancies could be due to the high polydispersity and the irregular shape of our Na-fluorohectorite particles, as well as diffusive double-layer effects, which could result in a competition between nematic ordering and gelation. The dependence on ionic strength displays three main regimes irrespective of clay concentration. At low ionic strength (approximately 0.1-5 mM NaCl), the Debye screening length is longer than the van der Waals force range. In this regime, the particles repel each other electrostatically and entropy-driven Onsager-type nematic ordering may occur, although gelation effects could also play a role. For ionic strengths above about 5 mM, we believe that the van der Waals force comes into play and that particles attract each other locally according to the classical Derjaguin, Landau, Verwey, and Overbeek (DLVO) model of colloid interactions, resulting in a small-domain regime of attractive nematiclike ordering. In the third regime, for ionic strengths above approximately 10 mM, the clay particles aggregate into larger assemblies, due to the dominant van der Waals force, and the observed birefringency is reduced. We have studied the nematic phase in detail between crossed polarizers and have found textures showing nematic Schlieren patterns. By rotating the polarizers as well as the samples, we have observed examples of disclinations of strengths -1, -1/2, and +1.
我们研究了合成的钠氟锂蒙脱石粘土悬浮液在盐溶液中重力诱导相分离的稳定层。我们观察了这些层如何依赖于粘土浓度以及盐含量。各向同性 - 向列相界面处的质量分布和密度变化表明,现有模拟中的现有模型和假设能够较好地解释观察到的行为。我们认为差异可能是由于我们的钠氟锂蒙脱石颗粒的高多分散性和不规则形状,以及扩散双层效应,这可能导致向列有序和凝胶化之间的竞争。无论粘土浓度如何,对离子强度的依赖性都表现出三种主要状态。在低离子强度(约0.1 - 5 mM NaCl)下,德拜屏蔽长度长于范德华力范围。在这种状态下,颗粒通过静电相互排斥,可能会发生熵驱动的昂萨格型向列有序,尽管凝胶化效应也可能起作用。对于高于约5 mM的离子强度,我们认为范德华力开始起作用,并且颗粒根据经典的德亚金、朗道、韦弗伊和奥弗贝克(DLVO)胶体相互作用模型在局部相互吸引,导致一种小区域的吸引性向列状有序状态。在第三种状态下,对于高于约10 mM的离子强度,由于占主导地位的范德华力,粘土颗粒聚集成更大的聚集体,观察到的双折射降低。我们在正交偏振器之间详细研究了向列相,发现了显示向列纹影图案的织构。通过旋转偏振器以及样品,我们观察到了强度为 -1、-1/2 和 +1 的位错示例。