SAXS reveals the magnetic alignment pathway of the goethite columnar liquid crystal phase.

The alignment of board-like colloidal goethite particles in the dense rectangular centred columnar liquid crystal phase in an external magnetic field is studied using small angle X-ray scattering (SAXS). Transient SAXS-patterns show broadening of the columnar reflections in specific directions. While the reflections along the field stay at a constant Q-value, the other reflections do not. These results imply a certain pathway of reorientation. It appears that alignment proceeds via collective rotation of domains inducing 'nanoshear' between the layers of particles, which slide over each other. The results support the recently suggested martensitic transition pathway for the simple and centred rectangular columnar phases, which were found to spontaneously transform into each other in another goethite system. The results also provide a fine example of how SAXS can be used to study reorientation behaviour of liquid crystals at the nanoscale.

Liquid crystal phase behavior of sterically-stabilized goethite.

The liquid crystalline phase behavior of sterically-stabilized goethite particles in toluene was studied using small-angle X-ray scattering. The results were compared with those from charged particles in water, with and without magnetic field: similarly rich phase behavior was found. Furthermore, the special magnetic properties were retained after coating the particles with amino-functionalized polyisobutylene chains. A remarkable difference between the aqueous and toluene samples is the latter's tendency to form gels. Smaller domains of the different liquid crystalline phases were observed and the columnar phase does not fully develop, furthermore a higher field is needed to align the full sample.

Simple rectangular columnar phase of goethite nanorods and its martensitic transition to the centered rectangular columnar phase.

Using high-resolution small-angle X-ray scattering, we observed a new type of the columnar phase with a simple rectangular (R(S)) structure in colloidal goethite dispersions. Furthermore, it displays a martensitic transition into the usual centered rectangular (R(C)) structure in an external magnetic field. The findings are rationalized in terms of entropic effects within a simple cell model. We interpret the results as an effect of the particle shape and the available degrees of freedom on the delicate balance between the space available for particle translations and rotations within the two structures.

Size fractionation in a phase-separated colloidal fluid.

Phase separation of a polydisperse colloidal dispersion implies size fractionation. An application of this effect is given by size-selective purification procedures associated with the colloidal synthesis of so-called monodisperse nanoparticles. We used electron microscopy to determine detailed particle size distributions of coexisting colloidal fluid phases containing highly polydisperse iron oxide nanoparticles with a log-normal distribution (sigma = 0.54 for the total system). Analysis of N approximately 10000 particles per phase yields the first five statistical moments of the distributions. Within experimental error, the interdependence of the statistical moments is in quantitative agreement with the "universal law of fractionation" proposed by Evans, Fairhurst, and Poon [Phys. Rev. Lett. 1998, 81, 1326], even though the theory was derived in the limit of slight polydispersity.