文摘
We have measured the linear rheology of critically purified ring polyisoprenes, polystyrenes, and polyethyleneoxides of different molar masses. The ratio of the zero-shear viscosities of linear polymer melts 畏0,linear to their ring counterparts 畏0,ring at isofrictional conditions is discussed as a function of the number of entanglements Z. In the unentangled regime 畏0,linear/畏0,ring is virtually constant, consistent with the earlier data, atomistic simulations, and the theoretical expectation 畏0,linear/畏0,ring = 2. In the entanglement regime, the Z-dependence of ring viscosity is much weaker than that of linear polymers, in qualitative agreement with predictions from scaling theory and simulations. The power-law extracted from the available experimental data in the rather limited range 1 < Z < 20, 畏0,linear/畏0,ring Z1.2卤0.3, is weaker than the scaling prediction (畏0,linear/畏0,ring Z1.6卤0.3) and the simulations (畏0,linear/畏0,ring Z2.0卤0.3). Nevertheless, the present collection of state-of-the-art experimental data unambiguously demonstrates that rings exhibit a universal trend clearly departing from that of their linear counterparts, and hence it represents a major step toward resolving a 30-year-old problem.