Published April 2006 | Version v1
Journal article

Magnetic-field-induced orientational order in the isotropic phase of hard colloidal platelets

  • 1. Van't Hoff Laboratory for Physical and Colloid Chemistry, Debye Institute, Utrecht University, Padualaan 8, 3584 CH Utrecht (Netherlands)
  • 2. Laboratoire de Physique des Solides, UMR 8502 CNRS, Universite Paris-Sud, Batiment 510, 91405 Orsay (France)
  • 3. Institut fuer Theoretische Physik II, Heinrich-Heine-Universitaet Duesseldorf, Universitaetsstrasse 1, Gebaeude 25.32, 40225 Duesseldorf (Germany)
  • 4. Netherlands Organisation for Scientific Research (NWO), DUBBLE CRG, European Synchrotron Radiation Facility, BP 220, 38043 Grenoble Cedex (France)

Description

The magnetic-field-induced orientational order in the isotropic phase of colloidal gibbsite [Al(OH)3] platelets is studied by means of optical birefringence and small-angle x-ray scattering (SAXS) techniques. The suspensions display field-induced ordering at moderate field strengths (a few Tesla), which increases with increasing particle concentration. The gibbsite particles align their normals perpendicular to the magnetic field and hence possess a negative anisotropy of their diamagnetic susceptibility Δχ. The results can be described following a simple, Onsager-like approach. A simplified model is derived that allows one to obtain the orientational distribution function directly from the scattering data. However, it leads to an underestimate of the diamagnetic susceptibility anisotropy Δχ. This accounts for the difference between the Δχ values provided by the two experimental techniques (SAXS and magneto-optics). The order of magnitude Δχ∼10-22 J/T2 lies in between that of goethite suspensions and that of suspensions of organic particles

Additional details

Identifiers

Publishing Information

Journal Title
Physical Review. E, Statistical Physics, Plasmas, Fluids, and Related Interdisciplinary Topics
Journal Volume
73
Journal Issue
4
Journal Page Range
p. 041402-041402.10
ISSN
1063-651X
CODEN
PLEEE8

Optional Information

Notes
(c) 2006 The American Physical Society