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Published on: June 10, 2018
Comparison of Cyclic and Linear Poly(lactide)s Using Small-Angle Neutron Scattering.
Philip B Yang1, Matthew G Davidson1,1, Karen J Edler1,2
1Institute for Sustainability and Department of Chemistry, University of Bath, Claverton Down, BathBA2 7AY, United Kingdom.
Cyclic and linear polylactide (PLA) polymers were studied using small-angle neutron scattering (SANS). Cyclic PLA exhibited more compact conformations due to its structure and hydrogen bonding, highlighting SANS as a tool for polymer topology characterization.
Area of Science:
- Polymer Science
- Materials Science
- Neutron Scattering
Background:
- Cyclic polymers are increasingly accessible, enabling new investigations into their properties.
- Small-angle neutron scattering (SANS) is a powerful technique for probing polymer chain configurations.
- Limited SANS data exists for cyclic polymers compared to linear counterparts.
Purpose of the Study:
- To compare chain configurations, scaling, and polymer-solvent interactions of cyclic and linear polylactide (PLA).
- To investigate the influence of polymer microstructure and molecular weight on these properties.
- To assess the utility of SANS for distinguishing cyclic polymer topology.
Main Methods:
- Small-angle neutron scattering (SANS) experiments.
- Utilized cyclic and linear polymers of racemic and l-lactides (PLA).
- Conducted experiments in acetone-d6 and THF-d8 at two temperatures.
Main Results:
- Observed significantly greater differences in effective polymer-solvent interaction parameters between cyclic and linear PLA.
- Found that cyclic PLA adopts more compact conformations, influenced by form factor and hydrogen bonding.
- Polymer microstructure substantially impacts polymer-solvent interaction parameters.
Conclusions:
- The distinct polymer-solvent interactions between cyclic and linear PLA depend heavily on the specific polymer.
- SANS is effective for identifying and characterizing cyclic polymer topology.
- Cyclic PLA's unique properties stem from its structure and intramolecular interactions.
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