Innovative and efficient preparation of high-performance polyacrylonitrile-based carbon fiber paper by centrifugal spinning
Source abstract
Abstract
Polyacrylonitrile (PAN) carbon fibers are often used to prepare high-performance paper-based materials owing to their high strength, good electrical and thermal conductivity, and superior comprehensive properties. In this study, a novel method for preparing PAN-based carbon fibers by centrifugal spinning was developed, and a stable and homogeneous PAN carbon fiber paper was successfully obtained. Subsequently, the formation process, microscopic morphology, electrical conductivity, electrochemical performance and hydrophobicity of the PAN carbon fiber paper were studied and evaluated. The results showed that the electrical conductivity of the PAN carbon fiber paper prepared via this method reached 43.250 s·cm −1 , resistivity was as low as 0.023–0.033 Ω·cm, and contact angle exceeded 140°. This study adopted a new method to prepare PAN carbon fiber paper, which provided another method for the preparation of high-performance fiber paper.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Supercapacitor Materials and Fabrication · Fiber-reinforced polymer composites · Electrospun Nanofibers in Biomedical Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of New Textile Materials & Advanced Processing Technology, Wuhan Textile University, China
Research and Development Department, Haiwei Composite Material Co., Ltd., China
College of Material Science and Engineering, Wuhan Textile University, China
Funding
The Key Research and Development Program of Hubei Province · National Natural Science Foundation of China
References (32)
Show source-provided references
1. 10.1016/S0016-2361(02)00166-710.1016/S0016-2361(02)00166-7 ↗
2. 10.7567/jjap.52.01ak0310.7567/jjap.52.01ak03 ↗
3. 10.1016/j.erss.2014.03.01010.1016/j.erss.2014.03.010 ↗
4. Valocchi M · 2014
5. 10.1016/j.renene.2015.01.02110.1016/j.renene.2015.01.021 ↗
6. 10.1016/j.electacta.2015.07.04410.1016/j.electacta.2015.07.044 ↗
7. 10.1016/j.biortech.2017.06.17010.1016/j.biortech.2017.06.170 ↗
8. 10.1021/acsami.0c2293010.1021/acsami.0c22930 ↗
9. 10.1039/c6ta02056a10.1039/c6ta02056a ↗
10. 10.1039/c0nr00470g10.1039/c0nr00470g ↗
11. 10.1002/app.4821810.1002/app.48218 ↗
12. 10.1016/j.jpowsour.2006.05.05310.1016/j.jpowsour.2006.05.053 ↗
13. 10.1016/j.jpowsour.2008.11.04610.1016/j.jpowsour.2008.11.046 ↗
14. 10.1016/j.polymer.2015.11.04610.1016/j.polymer.2015.11.046 ↗
15. 10.1016/j.jpowsour.2014.09.13010.1016/j.jpowsour.2014.09.130 ↗
16. 10.1007/s10853-019-04215-y10.1007/s10853-019-04215-y ↗
17. 10.1016/j.polymer.2016.02.02910.1016/j.polymer.2016.02.029 ↗
18. 10.1002/app.4607210.1002/app.46072 ↗
19. 10.1080/10408436.2022.208064010.1080/10408436.2022.2080640 ↗
20. 10.1016/j.matdes.2016.11.01910.1016/j.matdes.2016.11.019 ↗
21. 10.1016/j.ijbiomac.2018.02.04710.1016/j.ijbiomac.2018.02.047 ↗
22. 10.1007/s10853-016-0030-510.1007/s10853-016-0030-5 ↗
23. 10.1016/j.jallcom.2018.04.14110.1016/j.jallcom.2018.04.141 ↗
24. 10.3390/polym1110155010.3390/polym11101550 ↗
25. 10.1021/acsapm.1c0186510.1021/acsapm.1c01865 ↗
26. 10.1103/PhysRevE.89.02301110.1103/PhysRevE.89.023011 ↗
27. 10.1016/j.carbon.2012.08.03810.1016/j.carbon.2012.08.038 ↗
28. 10.1016/j.msec.2019.11015110.1016/j.msec.2019.110151 ↗
29. 10.1038/s41598-022-15085-x10.1038/s41598-022-15085-x ↗
30. 10.1039/C5TA08433D10.1039/C5TA08433D ↗
31. 10.1016/j.jmrt.2019.08.01910.1016/j.jmrt.2019.08.019 ↗
32. 10.1016/j.corsci.2017.10.02510.1016/j.corsci.2017.10.025 ↗