Interplay between end-association and entanglement in hydrogen-bonded telechelic polymers: A sticky situation
- Creators
- Takagi, Akira
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Kornfield, Julia A.
Abstract
A relatively new class of supramols.-highly entangled, end-functional polymers-are accessible through efficient ROMP+CTA (ring-opening metathesis polymn. with chain transfer agents) synthesis. At high concn. or in the melt, assocn. among the end-groups of entangled chains (>25 M_e) frustrates their reptation relaxation. This broadens the time range in which the materials behave in an elastomeric manner. The activation energy of end-assocn. can be tuned using polyvalent hydrogen bonding. Here, we compare polybutadienes that have either two or four carboxylate groups at each end. The activation energy for end-assocn. controls the time scale and temp. dependence of the terminal relaxation. For example, having two carboxylates at each end slows the terminal relaxation of a 50kg/mol PB by three orders of magnitude at ambient temp.-and by more than four orders of magnitude at 5°C. Thus, the terminal relaxation shifts more strongly with temp. than the chain segmental motion, giving an enlightening failure of time-temp. superposition. Two relaxation modes are evident: a "fast mode" assigned to the rearrangement of entangled chains constrained by end assocn. and a "slow mode" assigned to the end group exchange. Adding short polybutadiene as a dilutent helps to expose the underlying dynamics and leads to interesting adhesive materials.
Additional Information
© 2014 American Chemical Society.Additional details
- Eprint ID
- 55956
- Resolver ID
- CaltechAUTHORS:20150323-084316686
- Created
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2015-03-23Created from EPrint's datestamp field
- Updated
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2019-10-03Created from EPrint's last_modified field