The Ultrasensitivity of Living Polymers

Ben O’Shaughnessy and Dimitrios Vavylonis
Phys. Rev. Lett. 90, 118301 – Published 20 March 2003

Abstract

Synthetic and biological living polymers are self-assembling chains whose chain length distributions (CLDs) are dynamic. We show these dynamics are ultrasensitive: Even a small perturbation (e.g., temperature jump) nonlinearly distorts the CLD, eliminating or massively augmenting short chains. The origin is fast relaxation of mass variables (mean chain length, monomer concentration) which perturbs CLD shape variables before these can relax via slow chain growth rate fluctuations. Viscosity relaxation predictions agree with experiments on the best-studied synthetic system, α-methylstyrene.

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  • Received 23 July 2002

DOI:https://doi.org/10.1103/PhysRevLett.90.118301

©2003 American Physical Society

Authors & Affiliations

Ben O’Shaughnessy1 and Dimitrios Vavylonis1,2

  • 1Department of Chemical Engineering, Columbia University, New York, New York 10027
  • 2Department of Physics, Columbia University, New York, New York 10027

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Issue

Vol. 90, Iss. 11 — 21 March 2003

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