Thermally conductive polyamide 6/carbon filler composites based on a hybrid filler system
Source abstract
Abstract
We explored the use of a hybrid filler consisting of graphite nanoplatelets (GNPs) and single walled carbon nanotubes (SWCNTs) in a polyamide 6 (PA 6) matrix. The composites containing PA 6, powdered GNP, and SWCNT were melt-processed and the effect of filler content in the single filler and hybrid filler systems on the thermal conductivity of the composites was examined. The thermal diffusivities of the composites were measured by the standard laser flash method. Composites containing the hybrid filler system showed enhanced thermal conductivity with values as high as 8.8 W (m · K)−1, which is a 35-fold increase compared to the thermal conductivity of pure PA 6. Thermographic images of heat conduction and heat release behaviors were consistent with the thermal conductivity results, and showed rapid temperature jumps and drops, respectively, for the composites. A composite model based on the Lewis–Nielsen theory was developed to treat GNP and SWCNT as two separate types of fillers. Two approaches, the additive and multiplicative approaches, give rather good quantitative agreement between the predicted values of thermal conductivity and those measured experimentally.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Thermal properties of materials · Carbon Nanotubes in Composites · Graphene research and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Division of Advanced Materials, Korea Research Institute of Chemical Technology, Daejeon 34114, Korea
Department of Polymer Science and Engineering, Kyungpook National University, Daegu 41566, Korea
Department of Chemical Convergence Materials and Nanomaterials Science and Engineering, University of Science and Technology, Daejeon 34113, Korea
References (36)
Show source-provided references
1. 10.1039/c0jm04007j10.1039/c0jm04007j ↗
2. 10.1002/app.2960210.1002/app.29602 ↗
3. 10.1002/app.3048410.1002/app.30484 ↗
4. 10.1002/adv.2016510.1002/adv.20165 ↗
5. 10.1002/pc.2001510.1002/pc.20015 ↗
6. 10.1002/app.2660710.1002/app.26607 ↗
7. 10.1021/jp071761s10.1021/jp071761s ↗
8. 10.1063/1.368717310.1063/1.3687173 ↗
9. 10.1002/pat.123610.1002/pat.1236 ↗
10. 10.1002/app.2702710.1002/app.27027 ↗
11. 10.1002/polb.2080110.1002/polb.20801 ↗
12. 10.1002/pc.2015110.1002/pc.20151 ↗
13. 10.1016/j.compositesa.2012.09.00810.1016/j.compositesa.2012.09.008 ↗
14. 10.1021/jp308556r10.1021/jp308556r ↗
15. 10.1016/j.compositesa.2012.06.00910.1016/j.compositesa.2012.06.009 ↗
16. 10.1016/j.carbon.2009.11.04010.1016/j.carbon.2009.11.040 ↗
17. 10.1002/adma.20080040110.1002/adma.200800401 ↗
18. 10.1021/ma101066p10.1021/ma101066p ↗
19. 10.1134/S106378500710018510.1134/S1063785007100185 ↗
20. 10.1016/j.polymertesting.2005.03.00710.1016/j.polymertesting.2005.03.007 ↗
21. 10.1016/j.polymer.2012.03.04610.1016/j.polymer.2012.03.046 ↗
22. 10.1016/j.carbon.2012.06.00910.1016/j.carbon.2012.06.009 ↗
23. 10.1002/app.1157210.1002/app.11572 ↗
24. 10.1002/app.1993.07049091410.1002/app.1993.070490914 ↗
25. 10.1002/pc.75007030210.1002/pc.750070302 ↗
26. 10.1016/0266-3538(85)90087-910.1016/0266-3538(85)90087-9 ↗
27. 10.1002/pen.76016090510.1002/pen.760160905 ↗
28. 10.1002/andp.1935416070510.1002/andp.19354160705 ↗
29. Ashton J E · 1969
30. 10.1002/app.2886910.1002/app.28869 ↗
31. 10.1002/app.1193810.1002/app.11938 ↗
32. 10.1021/i160049a00410.1021/i160049a004 ↗
33. 10.1002/app.1973.07017122410.1002/app.1973.070171224 ↗
34. 10.1016/j.polymer.2010.10.05910.1016/j.polymer.2010.10.059 ↗
35. 10.1016/j.polymer.2009.12.04710.1016/j.polymer.2009.12.047 ↗
36. 10.1002/pi.453410.1002/pi.4534 ↗