Publication | Closed Access
Dynamics of a Polymer Solution in a Rigid Matrix
14
Citations
19
References
1998
Year
EngineeringMechanical EngineeringResponsive PolymersBiomedical EngineeringSoft MatterAgarose HydrogelsPolymersHydrogelsOsmotic PressureMechanicsRigid Agarose MatrixPolymer PhysicRheologyPolymer ChemistryBiophysicsBiopolymersBiopolymer GelColloid ChemistryMacromolecular SciencePolymer SolutionPolymer SciencePolymer ModelingRigid Matrix
We report dynamic light scattering measurements of solutions of a low molecular weight polymer (dextran Mw = 70 000), both in the free state and inside agarose hydrogels of varying concentrations. The light scattered from the rigid agarose matrix strongly heterodynes the signal from the mobile component, thereby allowing measurements both of the diffusion coefficient Dc and of the Rayleigh ratio Rθ of the dextran. For dextran concentrations c less than or equal to the overlap concentration c*, Dc decreases as the concentration of the gel matrix cg increases. The product DcRθ, which depends only on hydrodynamic factors, is, however, independent of the agarose concentration. It is concluded that the principal influence of the static gel matrix is to reduce the entropy and hence the osmotic pressure of the dextran solution. For concentrations of dextran greater than c*, the gel structure undergoes a phase separation.
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