Synthesis and characterization of high-temperature resistant and thermally conductive magnetic PBI/Fe3O4 nanofibers

2020 ◽  
Vol 32 (9) ◽  
pp. 1031-1042
Author(s):  
İlkay Özaytekin ◽  
Kamil Oflaz

In the present study, magnetite nanoparticles were added to an electrospinning solution of polyvinylidene fluoride (PVDF)/polybenzimidazole (PBI) polymers to prepare PBI/Fe3O4 nanofibers (NFs). The operating voltage of the electrospinning device was set to 15 kV, the distance between the needle and the plate was 10 cm, and the feed rate was set to 0.3 mL h−1. The microstructures of the as-prepared NFs were investigated by Fourier transform infrared spectrophotometry, atomic force microscopy, thermogravimetric analysis, and vibration sample magnetometry. Magnetite-doped PVDF/PBI NFs exhibited superior magnetism and saturation magnetization in the range of 1.5–5 emu g−1. It was observed that the thermal resistance of the fibers increased with the increasing amount of magnetic particles and nanocomposite fiber (NCF) 1 and NCF2 exhibited excellent thermal resistance up to 415°C and 450°C, respectively. The heat conduction coefficient of the fibers was measured at 4, 6, and 8 W. The thermal conductivity of the NFs increased with the increasing amount of magnetite nanoparticles, and the highest thermal conductivity coefficient for NCF2 (1.83 W mK−1) was measured at 4 W.

2018 ◽  
Vol 141 (1) ◽  
Author(s):  
Matthew Ralphs ◽  
Chandler Scheitlin ◽  
Robert Y. Wang ◽  
Konrad Rykaczewski

Thermally conductive soft composites are in high demand, and aligning the fill material is a potential method of enhancing their thermal performance. In particular, magnetic alignment of nickel particles has previously been demonstrated as an easy and effective way to improve directional thermal conductivity of such composites. However, the effect of compression on the thermal performance of these materials has not yet been investigated. This work investigates the thermal performance of magnetically aligned nickel fibers in a soft polymer matrix under compression. The fibers orient themselves in the direction of the applied magnetic field and align into columns, resulting in a 3× increase in directional thermal conductivity over unaligned composites at a volume fraction of 0.15. Nevertheless, these aligned fiber columns buckle under strain resulting in an increase in the composite thermal resistance. These results highlight potential pitfalls of magnetic filler alignment when designing soft composites for applications where strain is expected such as thermal management of electronics.


Membranes ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 895
Author(s):  
Ya Li ◽  
Yu Wang ◽  
Peng Chen ◽  
Ru Xia ◽  
Bin Wu ◽  
...  

With a trend of continuing improvement in the development of electronic devices, a problem of serious heat accumulation has emerged which has created the need for more efficient thermal management. Graphene sheets (GNS) have drawn much attention with regard to heat transfer because of their excellent in-plane thermal conductivity; however, the ultrahigh interfacial thermal resistance between graphene lamellae has seriously restricted its practical applications. Herein, we describe heat transfer membranes composed of graphene which have been modified by intrinsic thermally conductive polymers with different molecular weights. The presence of macromolecular surface modifiers not only constructed the graphene heat transfer interface by π–π interactions, but also significantly enhanced the membranes’ in-plane thermal conductivity by utilizing their intrinsic heat transfer properties. Such results indicated that the in-plane thermal conductivity of the fabricated membrane exhibits a high in-plane thermal conductivity of 4.17 W m−1 K−1, which, containing the GNS modified with 6000 g/mol (Mn) of poly(3-hexylthiophene) (P3HT), was 26 times higher that of poly (vinylidene fluoride) (PVDF). The P3HT molecular chain with specific molecular weight can form more matching structure π–π interactions, which promotes thermal conductivity. The investigation of different molecular weights has provided a new pathway for designing effective interfacial structures to relieve interface thermal resistance in thermally conductive membranes.


Polymers ◽  
2021 ◽  
Vol 13 (23) ◽  
pp. 4074
Author(s):  
Duanwei Zhang ◽  
Fusheng Liu ◽  
Sheng Wang ◽  
Mengxi Yan ◽  
Xin Hu ◽  
...  

This article proposes a method of increasing thermal conductivity (λ) by improving the λ value of a matrix and reducing the interfacial thermal resistance between such matrix and its thermally conductive fillers. D-GQDs (graphene quantum dots modified by polyetheramine D400) with a π–π-conjugated system in the center of their molecules, and polyether branched chains that are rich in amino groups at their edges, are designed and synthesized. AlN/DG-ER (AlN/D-GQDs-Epoxy resin) thermally conductive composites are obtained using AlN as a thermally conductive and insulating filler, using D-GQDs-modified epoxy resin as a matrix. All of the thermal conductivity, electrically insulating and physical–mechanical properties of AlN/DG-ER are investigated in detail. The results show that D-GQDs linked to an epoxy resin by chemical bonds can increase the value of λ of the epoxy–resin matrix and reduce the interfacial thermal resistance between AlN and DG-ER (D-GQDs–epoxy resin). The prepared AlN/DG-ER is shown to be a good thermally conductive and insulating packaging material.


2021 ◽  
Vol 13 (1) ◽  
Author(s):  
Junwei Gu ◽  
Kunpeng Ruan

AbstractRapid development of energy, electrical and electronic technologies has put forward higher requirements for the thermal conductivities of polymers and their composites. However, the thermal conductivity coefficient (λ) values of prepared thermally conductive polymer composites are still difficult to achieve expectations, which has become the bottleneck in the fields of thermally conductive polymer composites. Aimed at that, based on the accumulation of the previous research works by related researchers and our research group, this paper proposes three possible directions for breaking through the bottlenecks: (1) preparing and synthesizing intrinsically thermally conductive polymers, (2) reducing the interfacial thermal resistance in thermally conductive polymer composites, and (3) establishing suitable thermal conduction models and studying inner thermal conduction mechanism to guide experimental optimization. Also, the future development trends of the three above-mentioned directions are foreseen, hoping to provide certain basis and guidance for the preparation, researches and development of thermally conductive polymers and their composites.


2020 ◽  
pp. 089270572096564
Author(s):  
Xiao Wang ◽  
Hui Lu ◽  
Jun Chen

In this work, ultra-high molecular weight polyethylene (UHMWPE)/natural flake graphite (NG) polymer composites with the extraordinary high thermal conductivity were prepared by a facile mixed-heating powder method. Morphology observation and X-ray diffraction (XRD) tests revealed that the NG flakes could be more tightly coated on the surface of UHMWPE granules by mixed-heating process and align horizontally (perpendicular to the hot compression direction of composites). Laser flash thermal analyzer (LFA) demonstrated that the thermal conductivity (TC) of composites with 21.6 vol% of NG reached 19.87 W/(m·K) and 10.67 W/(m·K) in the in-plane and through-plane direction, respectively. Application experiment further demonstrated that UHMWPE/NG composites had strong capability to dissipate the heat as heat spreader. The obtained results provided a valuable basis for fabricating high thermal conductive composites which can act as advanced thermal management materials.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Aastha Vasdev ◽  
Moinak Dutta ◽  
Shivam Mishra ◽  
Veerpal Kaur ◽  
Harleen Kaur ◽  
...  

AbstractA remarkable decrease in the lattice thermal conductivity and enhancement of thermoelectric figure of merit were recently observed in rock-salt cubic SnTe, when doped with germanium (Ge). Primarily, based on theoretical analysis, the decrease in lattice thermal conductivity was attributed to local ferroelectric fluctuations induced softening of the optical phonons which may strongly scatter the heat carrying acoustic phonons. Although the previous structural analysis indicated that the local ferroelectric transition temperature would be near room temperature in $${\text {Sn}}_{0.7}{\text {Ge}}_{0.3}{\text {Te}}$$ Sn 0.7 Ge 0.3 Te , a direct evidence of local ferroelectricity remained elusive. Here we report a direct evidence of local nanoscale ferroelectric domains and their switching in $${\text {Sn}}_{0.7}{\text {Ge}}_{0.3}{\text {Te}}$$ Sn 0.7 Ge 0.3 Te using piezoeresponse force microscopy(PFM) and switching spectroscopy over a range of temperatures near the room temperature. From temperature dependent (250–300 K) synchrotron X-ray pair distribution function (PDF) analysis, we show the presence of local off-centering distortion of Ge along the rhombohedral direction in global cubic $${\text {Sn}}_{0.7}{\text {Ge}}_{0.3}{\text {Te}}$$ Sn 0.7 Ge 0.3 Te . The length scale of the $${\text {Ge}}^{2+}$$ Ge 2 + off-centering is 0.25–0.10 Å near the room temperatures (250–300 K). This local emphatic behaviour of cation is the cause for the observed local ferroelectric instability, thereby low lattice thermal conductivity in $${\text {Sn}}_{0.7}{\text {Ge}}_{0.3}{\text {Te}}$$ Sn 0.7 Ge 0.3 Te .


Sign in / Sign up

Export Citation Format

Share Document