High-Strength Self-Healing Polyurethane Composites Reinforced by Hydrogen Bonds

Striving to enhance the equilibrium between the mechanical attributes and self-healing capabilities of self-healing materials has remained a formidable challenge. Hydrogen bond-type self-healing materials have drawn an increasing amount of attention. Herein, we incorporated uracil units (UPy), which possess multiplicity functional groups conducive to the formation of hydrogen bond density, into the polyurethane (PU) matrix as a part of the chain extender. High hydrogen bond density inside the PUUPy material has a great contribution to achieve faster self-healing through reconstruction of hydrogen bonds and shortening self-healing time. Consequently, the initial mechanical properties of the severed PUUPy material are fully restored at lower temperatures with a faster self-healing time (80 °C, 1 h). The tensile strength and toughness of the PUUPy composite (5 wt % UPy) were increased by 12.82% (17.6 from 15.6 MPa of PU) and 91.6% (75.6 from 39.5 MJ m–3 of PU), respectively. For further obtaining high-strength self-healing polyurethane composites, hydroxylated boron nitride nanosheets (BNNS–OH) were introduced to PUUPy composites reforming an interface hydrogen bond, which can effectively transfer stress and enhance the strength of the PUUPy/BNNS–OH composites. The developed PUUPy/BNNS–OH (20 wt %) composite has significantly enhanced the tensile strength and toughness of the material to 24 MPa and 83.5 MJ m–3 and can lift the weight of 10,000 times its own weight after self-healing, showing its excellent mechanical properties. The heat transfer tube filled with the superstretchable, durable, and self-healing PUUPy/BNNS–OH composite placed on a 100 °C plate-type heater could reach a temperature difference of close to 40 °C compared to the commercial PU and Cu pad, which can be attributed to eliminating the interface thermal resistance caused by microbubbles. Therefore, its high strength, high toughness, and faster self-healing ability make it a promising candidate for further thermal management applications in portable electronics.

Authors

Institutions

Publication Details

Journal
ACS Applied Polymer Materials
Published
2025-05-28
DOI
https://doi.org/10.1021/acsapm.5c00639
Citations
5
Primary Topic
Polymer composites and self-healing
Type
article
Field-Weighted Citation Impact
3.03

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

High-Strength Self-Healing Polyurethane Composites Reinforced by Hydrogen Bonds

Xinyu Shao, Shudong Zhang, Liu Cui, Zhenyang Wang et al.
5 citations
ACS Applied Polymer Materials
Polymer composites and self-healing
3.03
article

High-Strength Self-Healing Polyurethane Composites Reinforced by Hydrogen Bonds

Xinyu Shao, Shudong Zhang, Liu Cui, Zhenyang Wang, Wei Guo, Nian Li, Jixiang Zhang
article en
5 citations

Abstract

Striving to enhance the equilibrium between the mechanical attributes and self-healing capabilities of self-healing materials has remained a formidable challenge. Hydrogen bond-type self-healing materials have drawn an increasing amount of attention. Herein, we incorporated uracil units (UPy), which possess multiplicity functional groups conducive to the formation of hydrogen bond density, into the polyurethane (PU) matrix as a part of the chain extender. High hydrogen bond density inside the PUUPy material has a great contribution to achieve faster self-healing through reconstruction of hydrogen bonds and shortening self-healing time. Consequently, the initial mechanical properties of the severed PUUPy material are fully restored at lower temperatures with a faster self-healing time (80 °C, 1 h). The tensile strength and toughness of the PUUPy composite (5 wt % UPy) were increased by 12.82% (17.6 from 15.6 MPa of PU) and 91.6% (75.6 from 39.5 MJ m–3 of PU), respectively. For further obtaining high-strength self-healing polyurethane composites, hydroxylated boron nitride nanosheets (BNNS–OH) were introduced to PUUPy composites reforming an interface hydrogen bond, which can effectively transfer stress and enhance the strength of the PUUPy/BNNS–OH composites. The developed PUUPy/BNNS–OH (20 wt %) composite has significantly enhanced the tensile strength and toughness of the material to 24 MPa and 83.5 MJ m–3 and can lift the weight of 10,000 times its own weight after self-healing, showing its excellent mechanical properties. The heat transfer tube filled with the superstretchable, durable, and self-healing PUUPy/BNNS–OH composite placed on a 100 °C plate-type heater could reach a temperature difference of close to 40 °C compared to the commercial PU and Cu pad, which can be attributed to eliminating the interface thermal resistance caused by microbubbles. Therefore, its high strength, high toughness, and faster self-healing ability make it a promising candidate for further thermal management applications in portable electronics.

ACS Applied Polymer MaterialsVol. 7(11)
Chinese Academy of Sciences (CN), Hefei Institutes of Physical Science (CN), Institute of Solid State Physics (CN), Chongqing Jiaotong University (CN)
Department of Science and Technology of Shandong Province, National Natural Science Foundation of China, Chinese Academy of Sciences, National Key Research and Development Program of China
Openalex Percentile: Top 9%
Polymer composites and self-healing
3.03
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.