DataVXPolymer CompositesPaper
journal article·2026-07-14

Synergistic Enhancement Mechanism of PDA ‐Modified h‐ BN on the Tribological Performance of Boron Phenolic Resin

Jingfu Song, Fan Xue, Siyuan Duan, Guoqing Wang, Qingjun Ding, Dae‐Eun Kim, Gai Zhao

Polymer Composites
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Source abstract

Abstract

ABSTRACT This study addresses the mechanical and tribological performance deficiencies of borophenolic resin (BPF)‐based frictional materials by surface‐modifying hexagonal boron nitride (h‐BN) with polydopamine (PDA). Composites with 6–10 wt% h‐BN@PDA were prepared to systematically evaluate the interfacial effects. The PDA layer improves h‐BN dispersion and interfacial bonding, thereby enhancing hardness, impact strength, and thermal conductivity. At the optimal 8 wt% loading, the wear rate reaches 4.76 × 10 −6 mm 3 /N m, a 54.62% reduction compared to the unmodified h‐BN. This study confirms the effectiveness of PDA surface modification in enhancing the mechanical‐thermal‐tribological synergy of BPF‐based composites, providing new insights for the design of high‐performance polymer‐based frictional materials.
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Research context

PolymersComposites

OpenAlex topics: Tribology and Wear Analysis · Brake Systems and Friction Analysis · Thermal properties of materials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

School of Naval Architecture & Ocean Engineering Jiangsu Maritime Institute Nanjing China

State Key Laboratory of Mechanics and Control for Aerospace Structures Nanjing University of Aeronautics and Astronautics Nanjing China

College of Mechanical and Electronic Engineering Nanjing Forestry University Nanjing China

Department of Mechanical Engineering Yonsei University Seoul Republic of Korea

Funding

National Natural Science Foundation of China · Nanjing University of Aeronautics and Astronautics · Priority Academic Program Development of Jiangsu Higher Education Institutions

References (33)

Show source-provided references
1. 10.1016/j.scib.2023.12.00310.1016/j.scib.2023.12.003 ↗
2. 10.1007/s40544‐021‐0581‐610.1007/s40544‐021‐0581‐6 ↗
3. 10.1016/j.triboint.2024.10988810.1016/j.triboint.2024.109888 ↗
4. 10.1016/j.jmrt.2023.08.21510.1016/j.jmrt.2023.08.215 ↗
5. 10.1016/j.compositesb.2023.11083310.1016/j.compositesb.2023.110833 ↗
6. 10.1016/j.actamat.2025.12080910.1016/j.actamat.2025.120809 ↗
7. 10.1007/s10904‐023‐02619‐710.1007/s10904‐023‐02619‐7 ↗
8. 10.1016/j.triboint.2019.10600110.1016/j.triboint.2019.106001 ↗
9. 10.3390/molecules2808340010.3390/molecules28083400 ↗
10. 10.1002/pat.602810.1002/pat.6028 ↗
11. 10.1016/j.compositesb.2018.12.03810.1016/j.compositesb.2018.12.038 ↗
12. 10.1177/095400831771031710.1177/0954008317710317 ↗
13. 10.1016/j.triboint.2014.09.01110.1016/j.triboint.2014.09.011 ↗
14. 10.1016/j.wear.2006.04.00410.1016/j.wear.2006.04.004 ↗
15. 10.1016/j.wear.2023.20514210.1016/j.wear.2023.205142 ↗
16. 10.1002/pi.529610.1002/pi.5296 ↗
17. 10.1016/j.msea.2006.03.10110.1016/j.msea.2006.03.101 ↗
18. 10.3390/ma1722547010.3390/ma17225470 ↗
19. 10.1002/pat.604310.1002/pat.6043 ↗
20. 10.1002/pc.2913610.1002/pc.29136 ↗
21. 10.1016/j.coco.2023.10173810.1016/j.coco.2023.101738 ↗
22. 10.1016/j.ceramint.2020.07.34010.1016/j.ceramint.2020.07.340 ↗
23. 10.3390/polym1004046110.3390/polym10040461 ↗
24. 10.3390/polym1206141010.3390/polym12061410 ↗
25. 10.1002/pen.7005010.1002/pen.70050 ↗
26. 10.1021/am507416y10.1021/am507416y ↗
27. 10.1016/j.sna.2019.06.03310.1016/j.sna.2019.06.033 ↗
28. 10.1002/pc.7008210.1002/pc.70082 ↗
29. 10.1038/s41598‐022‐26729‐310.1038/s41598‐022‐26729‐3 ↗
30. 10.1021/acsomega.3c0519810.1021/acsomega.3c05198 ↗
31. 10.1007/s40544‐019‐0269‐310.1007/s40544‐019‐0269‐3 ↗
32. 10.1039/c2py00612j10.1039/c2py00612j ↗
33. 10.1039/d2ra06669f10.1039/d2ra06669f ↗