Strong, self‐healing gelatin hydrogels cross‐linked by double dynamic covalent chemistry

A self-healing hydrogel ionic conductor has been developed by combining dynamic covalent chemistry with nanofiller reinforcement and micelle crosslinking, and used for sensing of diverse human activities.

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Design of Self-healing Polymers and High Value-added Urethane-containing Rubber Materials Based on Dynamic Covalent Chemistry

NIPPON GOMU KYOKAISHI ◽

10.2324/gomu.94.33 ◽

2021 ◽

Vol 94 (2) ◽

pp. 33-38

Author(s):

Hideyuki Hideyuki OTSUKA ◽

Daisuke AOKI ◽

Yasuhiro SHODA ◽

Katsuhiko TSUNODA

Keyword(s):

Value Added ◽

Self Healing ◽

Dynamic Covalent Chemistry

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Ultra-fast self-healing PVA organogels based on dynamic covalent chemistry for dye selective adsorption

New Journal of Chemistry ◽

10.1039/c9nj00891h ◽

2019 ◽

Vol 43 (20) ◽

pp. 7701-7707 ◽

Cited By ~ 6

Author(s):

Shujing Ren ◽

Panpan Sun ◽

Aoli Wu ◽

Na Sun ◽

Lixin Sun ◽

...

Keyword(s):

Methylene Blue ◽

High Efficiency ◽

Selective Adsorption ◽

Self Healing ◽

Dynamic Covalent Chemistry

Organogels can repair the damage rapidly, and the relative xerogels can adsorb methylene blue with high efficiency.

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Investigating the Self-Healing of Dynamic Covalent Thermoset Polyimine and Its Nanocomposites

Journal of Applied Mechanics ◽

10.1115/1.4044088 ◽

2019 ◽

Vol 86 (10) ◽

Author(s):

Chuanqian Shi ◽

Zhanan Zou ◽

Zepeng Lei ◽

Xingli Wu ◽

Zhengwei Liu ◽

...

Keyword(s):

Electrical Conductivity ◽

Shear Strength ◽

Environmental Pollution ◽

Interfacial Shear Strength ◽

Interfacial Shear ◽

The Self ◽

Self Healing ◽

Dynamic Covalent Chemistry ◽

Healing Effect ◽

Press Time

Self-healable and recyclable materials and electronics can improve the reliability and repairability and can reduce environmental pollution; therefore, they promise very broad applications. In this study, we investigated the self-healing performance of dynamic covalent thermoset polyimine and its nanocomposites based on the dynamic covalent chemistry. Heat press was applied to two laminating films of polyimine and its nanocomposites to induce self-healing. The effects of heat press time, temperature, and load on the interfacial shear strength of the rehealed films were investigated. The results showed that increasing the heat press time, temperature, and load can significantly improve the interfacial shear strength and thus the self-healing effect. For polyimine nanocomposites, increasing the heat press time, temperature, and load led to the improved electrical conductivity of the rehealed films.

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Bioinspired Self-Healing Hydrogel Based on Benzoxaborole-Catechol Dynamic Covalent Chemistry for 3D Cell Encapsulation

ACS Macro Letters ◽

10.1021/acsmacrolett.8b00434 ◽

2018 ◽

Vol 7 (8) ◽

pp. 904-908 ◽

Cited By ~ 72

Author(s):

Yangjun Chen ◽

Diana Diaz-Dussan ◽

Di Wu ◽

Wenda Wang ◽

Yi-Yang Peng ◽

...

Keyword(s):

Cell Encapsulation ◽

Self Healing ◽

Dynamic Covalent Chemistry

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Self-Healing Injectable Polymer Hydrogel via Dynamic Thiol-Alkynone Double Addition Crosslinks

10.26434/chemrxiv.11912577 ◽

2020 ◽

Author(s):

bowen fan ◽

Kai Zhang ◽

Qian Liu ◽

Rienk Eelkema

Keyword(s):

Polymer Network ◽

Star Polymer ◽

Cytotoxicity Test ◽

Self Healing ◽

Polymer Hydrogel ◽

Dynamic Covalent Chemistry ◽

Hydrogel Network ◽

New Type ◽

Aqueous Conditions ◽

Injectable Polymer

<p>Introduction of dynamic thiol-alkynone double addition crosslinks in a polymer network enable the formation of a self-healing injectable polymer hydrogel. A 4-arm polyethylene glycol (PEG) tetra-thiol star polymer is crosslinked by a small molecule alkynone via the thiol-alkynone double adduct, to generate a hydrogel network under ambient aqueous conditions (buffer pH=7.4 or 8.2, room temperature). The mechanical properties of these hydrogels can be easily tuned by varying the concentration of polymer precursors. Through the dynamic thiol-alkynone double addition crosslink, these hydrogels are self-healing and shear thinning, as demonstrated by rheological measurements, macroscopic self-healing and injection tests. These hydrogels can be injected through a 20G syringe needle and recover after extrusion. In addition, good cytocompatibility of these hydrogels is confirmed by cytotoxicity test. This work shows the application of a new type of dynamic covalent chemistry in the straightforward preparation of self-healing injectable hydrogels, which may find future biomedical applications such as tissue engineering and drug delivery.</p>

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Self-Healing Injectable Polymer Hydrogel via Dynamic Thiol-Alkynone Double Addition Crosslinks

10.26434/chemrxiv.11912577.v1 ◽

2020 ◽

Author(s):

bowen fan ◽

Kai Zhang ◽

Qian Liu ◽

Rienk Eelkema

Keyword(s):

Polymer Network ◽

Star Polymer ◽

Cytotoxicity Test ◽

Self Healing ◽

Polymer Hydrogel ◽

Dynamic Covalent Chemistry ◽

Hydrogel Network ◽

New Type ◽

Aqueous Conditions ◽

Injectable Polymer

<p>Introduction of dynamic thiol-alkynone double addition crosslinks in a polymer network enable the formation of a self-healing injectable polymer hydrogel. A 4-arm polyethylene glycol (PEG) tetra-thiol star polymer is crosslinked by a small molecule alkynone via the thiol-alkynone double adduct, to generate a hydrogel network under ambient aqueous conditions (buffer pH=7.4 or 8.2, room temperature). The mechanical properties of these hydrogels can be easily tuned by varying the concentration of polymer precursors. Through the dynamic thiol-alkynone double addition crosslink, these hydrogels are self-healing and shear thinning, as demonstrated by rheological measurements, macroscopic self-healing and injection tests. These hydrogels can be injected through a 20G syringe needle and recover after extrusion. In addition, good cytocompatibility of these hydrogels is confirmed by cytotoxicity test. This work shows the application of a new type of dynamic covalent chemistry in the straightforward preparation of self-healing injectable hydrogels, which may find future biomedical applications such as tissue engineering and drug delivery.</p>

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Self-healing alginate–gelatin biohydrogels based on dynamic covalent chemistry: elucidation of key parameters

Materials Chemistry Frontiers ◽

10.1039/c6qm00066e ◽

2017 ◽

Vol 1 (1) ◽

pp. 73-79 ◽

Cited By ~ 31

Author(s):

Asja Pettignano ◽

Marleen Häring ◽

Luca Bernardi ◽

Nathalie Tanchoux ◽

Françoise Quignard ◽

...

Keyword(s):

The Self ◽

Self Healing ◽

Dynamic Covalent Chemistry

Key parameters that govern the self-healing character of alginate–gelatin biohydrogels based on dynamic covalent chemistry have been elucidated.

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Self-healing, recyclable, and shape memory UV-curable coatings derived from tung oil and malic acid

Green Chemistry ◽

10.1039/d1gc01726h ◽

2021 ◽

Author(s):

Jinshuai Zhang ◽

Jia Huang ◽

Guoqiang Zhu ◽

Xixi Yu ◽

Jianwen Cheng ◽

...

Keyword(s):

Shape Memory ◽

Malic Acid ◽

Renewable Resources ◽

Microwave Assisted Synthesis ◽

Self Healing ◽

Uv Curable ◽

Dynamic Covalent Chemistry ◽

Tung Oil ◽

Microwave Assisted ◽

Smart Coatings

This study reports the development of super “green” smart coatings by integrating renewable resources, microwave-assisted synthesis, and dynamic covalent chemistry into UV-curable coatings. First, a novel UV-curable oligomer (TMG) was...

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