Unravelling the Mechanism of Viscoelasticity in Polymers with Phase-Separated Dynamic Bonds
Source abstract
Abstract
Incorporation of dynamic (reversible) bonds within polymer structure enables properties such as self-healing, shape transformation, and recyclability. These dynamic bonds, sometimes refer as stickers, can form clusters by phase-segregation from the polymer matrix. These systems can exhibit interesting viscoelastic properties with an unusually high and extremely long rubbery plateau. Understanding how viscoelastic properties of these materials are controlled by the hierarchical structure is crucial for engineering of recyclable materials for various future applications. Here we studied such systems made from short telechelic polydimethylsiloxane chains by employing a broad range of experimental techniques. We demonstrate that formation of a percolated network of interfacial layers surrounding clusters enhances mechanical modulus in these phase-separated systems, whereas single chain hopping between the clusters results in macroscopic flow. On the basis of the results, we formulated a general scenario describing viscoelastic properties of phase-separated dynamic polymers, which will foster development of recyclable materials with tunable rheological properties.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Polymer composites and self-healing · Advanced Polymer Synthesis and Characterization · Polymer Surface Interaction Studies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Material Science and Engineering, University of Tennessee, Knoxville, Tennessee 37996, United States
Department of Chemistry, University of Tennessee, Knoxville, Tennessee 37996, United States
The Bredesen Center for Interdisciplinary Research and Graduate Education, University of Tennessee, Knoxville, Tennessee 37996, United States
Chemical Sciences Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37830, United States
Funding
Division of Materials Research
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