4.7 Article

Enhanced Mechanical Properties of Aliphatic Polyester Thermoplastic Elastomers through Star Block Architectures

Journal

MACROMOLECULES
Volume 54, Issue 20, Pages 9327-9340

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.macromol.1c01357

Keywords

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Funding

  1. Northwestern University
  2. E.I. DuPont de Nemours Co.
  3. Dow Chemical Company
  4. U.S. DOE Office of Science by the Argonne National Laboratory [DE-AC02-06CH11357]
  5. NSF Center for Sustainable Polymers [CHE-1901635]

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The study found that star-shaped polymers outperformed linear polymers in terms of ultimate tensile strength, tensile toughness, and recovery characteristics, demonstrating the impact of polymer architecture on TPE mechanical properties. In the field of sustainable materials, simple changes in macromolecular architecture can significantly enhance material performance.
A series of sustainable aliphatic polyester thermoplastic elastomers (APTPEs) consisting of multi-arm star polymers with arms of poly(L-lactide)-b-poly(gamma-methyl-epsilon-caprolactone) were investigated and compared to analogous linear poly(L-lactide)-b-poly(gamma-methyl-epsilon-caprolactone)-b-poly(L-lactide) triblock polymers. Linear analogues with comparable arm molar mass and comparable overall molar mass were synthesized to distinguish architectural and molar mass effects. Overall, the star block polymers significantly outperformed their linear analogues with respect to ultimate tensile strength and tensile toughness, exhibiting more pronounced strain hardening than corresponding linear APTPEs. The stars exhibited high ultimate tensile strengths (similar to 33 MPa) and large elongations at break (similar to 1400%), outperforming commercially relevant, petroleum-derived, and non-degradable styrenic TPEs. The star polymers also exhibited superior recovery characteristics during cyclic strain cycles and reduced stress relaxation compared to the linear APTPEs, highlighting the impact of architecture on improved TPE mechanical properties. Dynamic mechanical thermal analysis suggests that the star architecture increases the usage temperature range and does not negatively influence processability, an important feature for future applications. Overall, this work illustrates that simple and convenient changes in the macromolecular architecture in sustainable APTPEs result in materials with greatly enhanced mechanical properties. A comprehensive understanding of the relationship between polymer architecture and mechanical properties can be capitalized on to develop property-specific and industrially relevant sustainable materials.

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