This is the authors' abstract. We don't add key points for this paper.
General rigid bead-rod theory [O. Hassager, J. Chem. Phys. 60, 4001 (1974)] explains polymer viscoelasticity from macromolecular orientation. By means of general rigid bead-rod theory, we relate the complex viscosity of polymeric liquids to the architecture of axisymmetric macromolecules. In this paper, we explore the complex viscosities of different axisymmetric diblock copolymer configurations. When nondimensionalized with the zero-shear viscosity, the diblock copolymer complex viscosity depends on the dimensionless frequency and the sole dimensionless architectural parameter, the macromolecular lopsidedness. In this paper, through this way, we thus compare the dimensionless relaxation time of different diblock macromolecular chains. We explore the effects of linear density, macromolecular length, and bead number ratio.
No takes yet. Share an insight, caveat, or question.
Kanso et al. (2020) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: