WEAR OF POLYTETRAFLUOROETHYLENE AND PTFE COMPOSITES

2009 ◽  
pp. 347-374 ◽  
Author(s):  
Thierry A. Blanchet
Keyword(s):  
Polymers ◽  
2021 ◽  
Vol 13 (14) ◽  
pp. 2332
Author(s):  
Ahmad Mamoun Khamis ◽  
Zulkifly Abbas ◽  
Raba’ah Syahidah Azis ◽  
Ebenezer Ekow Mensah ◽  
Ibrahim Abubakar Alhaji

The purpose of this study was to improve the dielectric, magnetic, and thermal properties of polytetrafluoroethylene (PTFE) composites using recycled Fe2O3 (rFe2O3) nanofiller. Hematite (Fe2O3) was recycled from mill scale waste and the particle size was reduced to 11.3 nm after 6 h of high-energy ball milling. Different compositions (5–25 wt %) of rFe2O3 nanoparticles were incorporated as a filler in the PTFE matrix through a hydraulic pressing and sintering method in order to fabricate rFe2O3–PTFE nanocomposites. The microstructure properties of rFe2O3 nanoparticles and the nanocomposites were characterized through X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), and high-resolution transmission electron microscopy (HRTEM). The thermal expansion coefficients (CTEs) of the PTFE matrix and nanocomposites were determined using a dilatometer apparatus. The complex permittivity and permeability were measured using rectangular waveguide connected to vector network analyzer (VNA) in the frequency range 8.2–12.4 GHz. The CTE of PTFE matrix decreased from 65.28×10−6/°C to 39.84×10−6/°C when the filler loading increased to 25 wt %. The real (ε′) and imaginary (ε″) parts of permittivity increased with the rFe2O3 loading and reached maximum values of 3.1 and 0.23 at 8 GHz when the filler loading was increased from 5 to 25 wt %. A maximum complex permeability of 1.1−j0.07 was also achieved by 25 wt % nanocomposite at 10 GHz.


2010 ◽  
Vol 654-656 ◽  
pp. 2763-2766 ◽  
Author(s):  
Li Wen Mu ◽  
Xin Feng ◽  
Yi Jun Shi ◽  
Huai Yuan Wang ◽  
Xiao Hua Lu

The tribological properties of polyimide (PI) composites reinforced with graphite or MoS2 sliding in liquid alkali and water as well as dry friction were investigated using a ring-on-ring tester. The results show that the friction coefficient (μ) and wear rate (W) for both graphite/PI and MoS2/PI composites in different liquid mediums are μdry>μwater >μalkali and Wwater>Wdry >Walkali. Results also indicate that the friction coefficient and wear rate of the PI composites filled with different solid lubricants are μMoS2 >μgraphite and W MoS2 >Wgraphite in different liquid mediums. In addition, the hydrophobic inorganic fillers are fit for the reinforcement of polymer-based composites sliding in liquid mediums. It is also concluded from the authors’ work that the wear rate and friction coefficient of polymer-based (such as PI, PTFE) composites in the alkali lubricated conditions is lowest among all the friction conditions. This may be attributed to the ionic hydration in the alkaline solution.


2013 ◽  
Vol 690-693 ◽  
pp. 1636-1640 ◽  
Author(s):  
Te Hsing Wu ◽  
Ko Shao Chen ◽  
Lie Hang Shen

In this study, We immobilized hydrogel material onto expanded polytetrafluoroethylene (ePTFE) film and used as an functional biomaterial. The material is a film containing titanium oxide onto polymer sheet. The hydrogel film is hydrophilic, bacterial inactivated and bio-compatible. In order to improve the ePTFE film biocompatibility, the cold plasma or γ-ray technology was used with acetic acid as monomer to deposit onto ePTFE film and then (N-isopropylacrylamide) was grafted onto the surface by radiation photo-grafting. The characteristics of the material surface were evaluated with X-ray photoelectron spectroscopy (XPS), FTIR and water contact angle. It was found that the contact angle of water on the untreated ePTFE significantly decrease from125° to 72° after ePTFE film being treated with acetic acid plasma deposition procedure. Due to the hydrophilicity of poly (N-isopropylacrylamide), so the contact angle of water on the ePTFE-g-NIPAAm almost approached to 0°. This thermal sensitive ePTFE hydrogels can be applied to artificial guiding tube and wound dressing material.


2012 ◽  
Vol 51 (4) ◽  
pp. 377-380 ◽  
Author(s):  
Gang Tang ◽  
Daofang Chang ◽  
Dongmei Wang ◽  
Junliang He ◽  
Weijian Mi ◽  
...  

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