Affiliations: Rheology Laboratory, Department of Mechanical Engineering, University of Texas at Austin, USA | Vilastic Scientific, Inc., Austin, TX, USA
Note: [] Address of correspondence: Dr. Nancy Henderson, Vilastic Scientific, Inc., P.O. Box 160261, Austin, TX 78716, USA. Tel.: +1 512 327 4134; Fax: +1 512 327 0655; E-mail: rheology@vilastic.com.
Abstract: The viscoelastic properties of blood are dominated by microstructures formed by red cells. The microstructures are of several types such as irregular aggregates, rouleaux, and layers of aligned cells. The dynamic deformability of the red cells, aggregation tendency, cell concentration, size of confining vessel and rate of flow are determining factors in the microstructure. Viscoelastic properties, viscosity and elasticity, relate to energy loss and storage in flowing blood while relaxation time and Weissenberg number play a role in assessing the importance of the elasticity relative to the viscosity. These effects are shown herein for flow in a large straight cylindrical tube, a small tube, and a porous medium. These cases approximate the geometries of the arterial system: large vessels, small vessels and vessels with many branches and bifurcations. In each case the viscosity, elasticity, relaxation time and Weissenberg number for normal human blood as well as blood with enhanced cell aggregation tendency and diminished cell deformability are given. In the smaller spaces of the microtubes and porous media, the diminished viscosity shows the possible influence of the Fåhraeus–Lindqvist effect and at high shear rates, the viscoelasticity of blood shows dilatancy. This is true for normal, aggregation enhanced and hardened cells.
Keywords: Viscosity, elasticity, relaxation time, sickle cell, aggregation, deformability
Journal: Biorheology, vol. 43, no. 6, pp. 729-746, 2006
