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Published December 15, 1998 | public
Journal Article

Rouse and Reptation Dynamics of Linear Polybutadiene Chains Studied by ^2H NMR Transverse Relaxation

Abstract

Deuterium NMR has been used to investigate two different types of dynamics of linear polybutadiene chains in the melt. The transverse relaxations of short Rouse chains of molecular weight 640−3000 were biexponential, which has been attributed to separate decays of the methylene and methine deuterons. Interpretation of the transverse relaxation rates using a model for Rouse dynamics, combined with molecular simulations, gave the shortest Rouse unit as approximately 4.4 monomers and the shortest Rouse time as 8.3 × 10^(-7) s. The reptation dynamics of higher molecular weight entangled chains were investigated using ABA isotopic triblock copolymers, of total molecular weight 14000−135000, where A is protonated polybutadiene of molecular weight greater than the entanglement molecular weight and B is a deuterated block. These polymers were specifically synthesized so that the fast motion of the Rouse-like chain ends should not complicate the signal. The fundamental parameters found for the Rouse chain were used in the reptation model, assuming fast dynamics, and gave an entanglement molecular weight, M_e, of 5380 or approximately 21 Rouse units. This M_e is more than twice the conventional value, obtained from rheology, and is more suggestive of the critical molecular weight M_c, consistent with previous NMR work. The theoretical analysis used in this work is based on the assumption that the chain dynamics are fast on the time scale set by the NMR deuterium quadrupolar interaction. The highest molecular weight samples were found to not satisfy this criterion and indicate the molecular weight at which a new theoretical approach is needed.

Additional Information

© 1998 American Chemical Society. Received April 1, 1998; Revised Manuscript Received July 7, 1998.

Additional details

Created:
August 19, 2023
Modified:
October 18, 2023