Mussel‐Inspired, Self‐Healing, Highly Effective Fully Polymeric Fire‐Retardant Coatings Enabled by Group Synergy

Author:

Ma Zhewen1,Feng Jiabing2,Huo Siqi2,Sun Ziqi3,Bourbigot Serge4,Wang Hao2,Gao Jiefeng5,Tang Long‐Cheng6,Zheng Wei1,Song Pingan27ORCID

Affiliation:

1. Interdisciplinary Materials Research Center College of Materials Science and Engineering Tongji University Shanghai 201804 China

2. Centre for Future Materials University of Southern Queensland Springfield 4300 Australia

3. School of Chemistry and Physics Queensland University of Technology 2 George Street Brisbane 4000 Australia

4. ENSCL UMR 8207 – UMET – Unité Matériaux et Transformations Univ. Lille 42 rue Paul. Duez Lille 59000 France

5. College of Chemistry and Chemical Engineering Yangzhou University Yangzhou 225002 China

6. College of Material Chemistry and Chemical Engineering Hangzhou Normal University Hangzhou 311121 China

7. School of Agriculture and Environmental Science University of Southern Queensland Springfield 4300 Australia

Abstract

AbstractFire‐retardant coatings represent a universal cost‐effective approach to providing fire protection for various substrates without compromising substrates’ bulk properties. However, it has been attractive yet highly challenging to create waterborne polymeric fire‐retardant coatings combining high‐efficiency, generally strong adhesion, and self‐repairability due to a lack of rational design principles. Inspired by mussel's unique adhesive, self‐healing, and char‐forming mechanisms, herein, a “group synergy” design strategy is proposed to realize the combination of self‐healing, strong adhesion, and high efficiency in a fully polymeric fire‐retardant coating via multiple synergies between catechol, phosphonic, and hydroxyethyl groups. As‐created fire‐retardant coating exhibits a rapid room‐temperature self‐healing ability and strong adhesion to (non)polar substrates due to multiple dynamic non‐covalent interactions enabled by these groups. Because these functional groups enable the formation of a robust structurally intact yet slightly expanded char layer upon exposure to flame, a 200 µm‐thick such coating can make extremely flammable polystyrene foam very difficult to ignite and self‐extinguishing, which far outperforms previous strategies. Moreover, this coating can provide universal exceptional fire protection for a variety of substrates from polymer foams, and timber, to fabric and steel. This work presents a promising material design principle to create next‐generation sustainable high‐performance fire‐retardant coatings for general fire protection.

Funder

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Australian Research Council

Publisher

Wiley

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