4.7 Article

Weldable and Reprocessable Biomimetic Polymer Networks Based on a Hydrogen Bonding and Dynamic Covalent Thiourea Motif

Journal

ACS APPLIED POLYMER MATERIALS
Volume 3, Issue 8, Pages 3714-3720

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsapm.1c00667

Keywords

covalent adaptable networks; biomimetic polymer networks; thiourea; dynamic covalent bond; hydrogen (H) bond

Funding

  1. Creative Materials Discovery Program [2019M3D1A210391621]
  2. Nano.Material T e c h n o l o g y D e v e l o p m e n t P r o g r a m [2021M3H4A1A03041426]
  3. National Research Foundation of Korea (NRF) - Ministry of Science and ICT
  4. Korea Research Institute of Chemical Technology (KRICT) core project [SS2121-20]

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Thiourea linkage is used as a hydrogen bonding and dynamic covalent dual-functional motif to enhance mechanical versatility in biomimetic polymer networks (BMPNs). By controlling the dynamic thiourea bond exchanges, improved malleability and reprocessability are achieved while maintaining various mechanical characteristics, enabling versatile shape manipulation and mechanical functions in BMPN-based 3D structures.
Here we describe the use of thiourea linkage as a hydrogen (H) bonding and dynamic covalent dual-functional motif to enhance mechanical versatility in biomimetic polymer networks (BMPNs). By controlling the dynamic thiourea bond exchanges in the covalently cross-linked BMPNs, greatly improved malleability and reprocessability are obtained while maintaining their assorted mechanical characteristics of stiffness, strength, toughness, resilience, and adaptability. Such characteristics enable versatile shape manipulation and mechanical functions of the BMPN-based 3D structures, including shape reconfiguration, welding, shape memory, load bearing, deformation/recovery, repair, and reprocessing.

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