Rubber composites composed of biobased epoxidized natural rubber and tunicate cellulose nanocrystals exhibited recyclable and self-healable capacities via transesterification reactions.
A robust, tough, and self-healable
elastomer is a promising candidate
for substrate in flexible electronic devices, but there is often a
trade-off between mechanical properties (robustness and toughness)
and self-healing. Here, a poly(dimethylsiloxane) (PDMS) supramolecular
elastomer is developed based on metal-coordinated bonds with relatively
high activation energy. The strong metal–coordination complexes
and their corresponding ionic clusters acting as the cross-linking
points strengthen the resultant supramolecular networks, which achieves
superior mechanical robustness (2.81 MPa), and their consecutive dynamic
rupture and reconstruction efficiently dissipate strain energy during
the stretching process, which leads to an impressive fracture toughness
(32 MJ/m3). Additionally, the reversible intermolecular
interactions (weak hydrogen bonds and strong sacrificial coordination
complexes/clusters) can break and re-form upon heating; thus, the
elastomer self-heals at a moderate temperature with the highest healing
efficiency of 95%. As such, the potential of the as-prepared supramolecular
elastomer for a substrate material of flexible electronic devices
is discovered.
Endowing
conductive composites with good self-healing properties
is of great significance for improving the stability and extending
the service life of the material. However, it is still a challenge
to prepare conductive composites that exhibit both desirable mechanical
strength and excellent self-healing properties. Herein, we report
a simple method to fabricate a kind of material with excellent self-healing
properties and satisfactory mechanical strength and conductivity performance.
Nanochitin (CNC), carboxymethyl chitosan (CMCS), and carbon nanotubes
(CNTs) were used as reinforcing fillers and filled into epoxidized
natural rubber (ENR) through latex mixing. In particular, CNCs, CMCS,
and CNT fillers were selectively dispersed among ENR latex particles.
A filler frame network structure based on multiple hydrogen bonding
interactions was constructed in the rubber matrix, which significantly
improved the mechanical and electrical properties of the composites.
Furthermore, the formation of multiple hydrogen bonds in the composites
endowed the rubber with excellent self-healing properties, achieving
the highest healing efficiency of 91%. This work provides a novel
and simple strategy to prepare conductive composites with excellent
mechanical and self-healing properties.
This experiment has preliminarily confirmed urinary CD80 as a non-invasive diagnostic biomarker. It may have significant value in the diagnosis of MCD.
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