Abstract

Covalent adaptable networks (CANs) are polymeric networks containing covalent crosslinks that are dynamic under specific conditions. In addition to possessing the malleability of thermoplastics and the dimensional stability of thermosets, CANs exhibit a unique combination of physical properties, including adaptability, self-healing, shape-memory, stimuli-responsiveness, and enhanced recyclability. The physical properties and the service conditions (such as temperature, pH, and humidity) of CANs are defined by the nature of their constituent dynamic covalent bonds (DCBs). In response to the increasing demand for more sophisticated and adaptable materials, the scientific community has identified dual dynamic networks (DDNs) as a promising new class of polymeric materials. By combining two (or more) distinct crosslinkers in one system, a material with tailored thermal, rheological, and mechanical properties can be designed. One remarkable ability of DDNs is their capacity to combine dimensional stability, bond dynamicity, and multi-responsiveness. This review aims to give an overview of the advances in the emerging field of DDNs with a special emphasis on their design, structure-property relationships, and applications. This review illustrates how DDNs offer many prospects that single (dynamic) networks cannot provide and highlights the challenges associated with their synthesis and characterization.

Highlights

  • Synthetic organic polymers have found use in an incredibly broad range of applications, spanning single-use packaging materials to specialized medical devices

  • Conclusions and Outlook network composed of reversible DA adducts is synthesized

  • This review provides an overview of the development of a new class of Covalent adaptable networks (CANs) that reaction allows for an efficient synthesis of the support network, while the retro Diels-Alder (rDA) reaction at incorporates multiple crosslinkers featuring different degrees of dynamicity

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Summary

Introduction

Synthetic organic polymers have found use in an incredibly broad range of applications, spanning single-use packaging materials to specialized medical devices. Thanks to the covalent nature of their interaction, DCBs tend to impart greater creep resistance to dynamically crosslinked materials when compared to NCBs. The physical properties of dynamic materials that incorporate just one kind of NCB or DCB strongly depend on the nature and kinetics of the bond exchanges within the polymer network. DCBs h exploited in most kinds of polymer materials ranging from 3 of 34 bulk m like polyurethane (PUR) thermoplastic elastomers (TPEs) and vitrimers to hydro hough it is difficult to form generalized principles for such a diverse field, it is c theAthoughtful of two kinds of crosslinks remarkably and large creative number ofcombination. Shape highlight variety of materials of of polyurethane elastomers, amaterials, brief overview presents the nature and the properties of DCBs as well as the CANs vitrimers, hydrogels, and interpenetrated polymer networks.in which they are integrated. After a brief discussion of the historical context of DDNs, we highlight a variety of materials in the fields of polyurethane elastomers, shape memory

Dynamic
Dynamic Covalent Bonds in Polymer Networks
Origin of Dual Dynamic Networks
Polyurethane Elastomers
Shape Memory Polymers
Vitrimers and CANs with Two Covalent Dynamic Crosslinking Strategies
Reinforcement by Supramolecular
Reinforcement by Static Covalent Bonds
10. Vitrimers
Hydrogels
Hydrogels Combining Dynamic Covalent Bonds and Supramolecular Interactions
Hydrogels with Dynamic Covalent Crosslinks of Different Natures
Networks Combining Two Different Structures
Interpenetrated Networks
Combined Networks
Combined
Findings
Conclusions and Outlook
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