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Chain model of electrorheology

Journal Article · · Journal of Chemical Physics
DOI:https://doi.org/10.1063/1.471176· OSTI ID:282008
;  [1]
  1. Research and Exploratory Technology Division, Sandia National Laboratories, Albuquerque, New Mexico 87185-1421 (United States)

We develop a chain model of an electrorheological fluid in steady and oscillatory shear. This model is based on a balance of hydrodynamic and electrostatic forces and focuses on the mechanical stability of chains. With this model we compute the shape and orientation of an unconfined dipolar chain in steady shear as a function of the shear rate and electric field, and show that this leads to the expected shear-thinning viscosity. We then demonstrate that chains confined by electrodes are unstable in some Mason number regimes. The chain model is extended to the case of oscillatory shear by including a kinetic equation for the aggregation and fragmentation of chains. The resultant chain dynamics is found to be strongly nonlinear, as is the rheology. Finally, we consider the effect of local field corrections and long range interactions on the bare dipolar interaction force and derive a self-consistent pair interaction force that demonstrates that the maximum orientation of a chain in shear depends strongly on the dielectric contrast. {copyright} {ital 1996 American Institute of Physics.}

Research Organization:
Sandia National Laboratory
DOE Contract Number:
AC04-76DR00789
OSTI ID:
282008
Journal Information:
Journal of Chemical Physics, Journal Name: Journal of Chemical Physics Journal Issue: 12 Vol. 104; ISSN JCPSA6; ISSN 0021-9606
Country of Publication:
United States
Language:
English

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