Mechanochemical Strengthening of a Synthetic Polymer in Response to Typically Destructive Shear Forces

Abstract

High shear stresses are known to trigger destructive bond-scission reactions in polymers. Recent work has shown that the same shear forces can be used to accelerate non-destructive reactions in mechanophores along polymer backbones, and it is demonstrated here that such mechanochemical reactions can be used to strengthen a polymer subjected to otherwise destructive shear forces. Polybutadiene was functionalized with dibromocyclopropane mechanophores, whose mechanical activation generates allylic bromides that are crosslinked in situ by nucleophilic substitution reactions with carboxylates. The crosslinking is activated efficiently by shear forces both in solvated systems and in bulk materials, and the resulting covalent polymer networks possess moduli that are orders-ofmagnitude greater than those of the unactivated polymers. These molecular-level responses and their impact on polymer properties have implications for the design of materials that, like biological materials, actively remodel locally as a function of their physical environment.

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Document Details

Document Type
Technical Report
Publication Date
Aug 04, 2013
Accession Number
ADA605645

Entities

People

  • Ashley L. Ramirez
  • Joshua A. Orlicki
  • Mangesh Champhekar
  • Sarah M. Elsakr
  • Stephen L Craig
  • Wendy E. Krause
  • Zachary S. Kean

Organizations

  • University of Illinois Urbana–Champaign

Tags

Communities of Interest

  • Energy and Power Technologies
  • Ground and Sea Platforms

DTIC Thesaurus Topics

  • Alkenes
  • Bulk Materials
  • Carboxylic Acids
  • Chemical Synthesis
  • Chemistry
  • Infrared Spectra
  • Infrared Spectroscopy
  • Materials
  • Mechanical Properties
  • Modulus Of Elasticity
  • Molecular Weight
  • Polymer Chemistry
  • Polymers
  • Shear Stresses
  • Spectra
  • Spectroscopy
  • Synthetic Polymers

Readers

  • Polymer Science and Technology
  • Quantum Chemistry
  • Structural Dynamics.