Self-healing thermally conductive adhesives
Source abstract
Abstract
Thermally conductive composites with a temperature-triggered self-healing response were produced by dispersing boron nitride or graphite particles into two types of polysulphide-based thermoset matrices. The composites produced exhibit recovery of both cohesion and adhesion properties upon thermally activated healing. Using a mild healing temperature (65°C), the materials show full recovery of their initial adhesive strength during multiple healing cycles. The composites behave differently regarding the cohesion recovery: 20%–100% recovery is achieved depending on the filler type, filler loading and the type of matrix. The thermal conductivity of the composites increases with the amount of filler. Values of 1 and 2 W/m K can be achieved for the boron nitride and graphite-based composite, respectively. The results presented in this work clearly show that multifunctional materials with different functionalities and mechanical self-healing responses can be designed using this strategy.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Polymer composites and self-healing · Synthesis and properties of polymers · Advanced Sensor and Energy Harvesting Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Materials Innovation Institute, Delft, The Netherlands
Novel Aerospace Materials, Faculty of Aerospace Engineering, Delft University of Technology, Delft, The Netherlands
DIMES, Faculty of Electrical Engineering, Mathematics and Computer Science, Delft University of Technology, Delft, The Netherlands
References (20)
Show source-provided references
1. 10.1002/anie.20100388810.1002/anie.201003888 ↗
2. 10.1023/B:JMSC.0000007726.58758.e410.1023/B:JMSC.0000007726.58758.e4 ↗
3. 10.1039/B713953P10.1039/B713953P ↗
4. 10.1016/j.polymer.2008.12.04010.1016/j.polymer.2008.12.040 ↗
5. 10.1146/annurev-matsci-070909-10453210.1146/annurev-matsci-070909-104532 ↗
6. 10.1021/ma200149210.1021/ma2001492 ↗
7. 10.1007/s10973-011-1760-x10.1007/s10973-011-1760-x ↗
8. 10.1021/ma021067510.1021/ma0210675 ↗
9. 10.1002/adma.20080200810.1002/adma.200802008 ↗
10. 10.1038/nature0666910.1038/nature06669 ↗
11. 10.1016/j.porgcoat.2011.06.01610.1016/j.porgcoat.2011.06.016 ↗
12. 10.1016/j.polymer.2010.10.04810.1016/j.polymer.2010.10.048 ↗
13. 10.1016/j.microrel.2011.08.01310.1016/j.microrel.2011.08.013 ↗
14. 10.1021/am301879z10.1021/am301879z ↗
15. 10.1126/science.121264810.1126/science.1212648 ↗
16. 10.1016/j.compositesa.2010.07.00810.1016/j.compositesa.2010.07.008 ↗
17. 10.1016/j.eurpolymj.2010.07.00810.1016/j.eurpolymj.2010.07.008 ↗
18. 10.1038/nnano.2012.19210.1038/nnano.2012.192 ↗
19. 10.1007/978-1-4020-6250-610.1007/978-1-4020-6250-6 ↗
20. 10.1109/ISAPM.2004.128798110.1109/ISAPM.2004.1287981 ↗