It is well known that dipole-dipole forces (induced by external electric fields) between colloidal particles play a central role in determining the thermodynamic phases of electrorheological fluids. Here, it is argued that the long-range van der Waals forces induced by photon exchange also play an important role. A theory, which quantitatively includes the van der Waals interactions, is developed using statistical thermodynamic mean-field approximations. A comparison with an experimental phase separation is shown to be satisfactory.
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Woestman et al. (1993) studied this question.
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