journal article·2024-07-01Open access

Ductile Glassy Polymer Networks Capable of Large Plastic Deformation and Heat-Induced Elastic Recovery

Caleb J. Reese, Grant M. Musgrave, Anna K. Huber, Sijia Huang, Eden Y. Yau, Chen Wang

ACS Materials Letters· Volume 6· Issue 7

Abstract

Many thermoplastic polymers are ductile by combining strength and large deformations. These deformations are irreversible ─ known as plastic deformation. Elastomers can deform reversibly but have low strength. To this end, we developed glassy and ductile polyamide networks capable of large plastic deformation (>200% strain) and high strength (∼50 MPa tensile strength and ∼1500 MPa Young’s modulus), similar to those of polyolefins and Nylon-66. We discovered that hydrogen bonding between meta-phthalamide groups was essential to the ductility. Since these polyamide networks are covalently bonded, we demonstrated their unique durability by repeatable elastic recovery at elevated temperatures, exhibiting indifferent tensile properties in each cycle. Furthermore, when we fixed the strain during the elastic recovery, these polyamide networks actuated stresses of 9–18 MPa, among the highest reported in shape-memory polymer actuators. We envision these ductile, glassy polymer networks as promising alternatives to ductile thermoplastics, given the combined benefit of ductility and durability.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Polymer composites and self-healing · Advanced Materials and Mechanics · Advanced Polymer Synthesis and Characterization

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Materials Science and Engineering, University of Utah, Salt Lake City, Utah 84112, United States

Lawrence Livermore National Laboratory, Livermore, California 94550, United States

Funding

University of Utah

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