scholarly journals Fabrication of Porous Carbon Films and Their Impact on Carbon/Polypropylene Interfacial Bonding

2021 ◽  
Vol 5 (4) ◽  
pp. 108
Author(s):  
Yucheng Peng ◽  
Ruslan Burtovyy ◽  
Rajendra Bordia ◽  
Igor Luzinov
Keyword(s):  
Porous Carbon ◽  
High Performance ◽  
Carbon Film ◽  
Interfacial Strength ◽  
Dip Coating ◽  
Carbon Films ◽  
Thermoplastic Composites ◽  
Graphite Substrate ◽  
Pore Former ◽  
Withdrawal Speed

Porous carbon films were generated by thermal treatment of polymer films made from poly(acrylonitrile-co-methyl acrylate)/polyethylene terephthalate (PAN/PET) blend. The precursor films were fabricated by a dip-coating process using PAN/PET solutions in hexafluoro-2-propanol (HFIP). A two-step process, including stabilization and carbonization, was employed to produce the carbon films. PET functioned as a pore former. Specifically, porous carbon films with thicknesses from 0.38–1.83 μm and pore diameters between 0.1–10 μm were obtained. The higher concentrations of PET in the PAN/PET mixture and the higher withdrawal speed during dip-coating caused the formation of larger pores. The thickness of the carbon films can be regulated using the withdrawal speed used in the dip-coating deposition. We determined that the deposition of the porous carbon film on graphite substrate significantly increases the value of the interfacial shear strength between graphite plates and thermoplastic PP. This study has shown the feasibility of fabrication of 3D porous carbon structure on the surface of carbon materials for increasing the interfacial strength. We expect that this approach can be employed for the fabrication of high-performance carbon fiber-thermoplastic composites.

Preparation of Porous Carbon Film and its Application in Li-Ion Battery

2011 ◽  
Vol 239-242 ◽  
pp. 528-531
Author(s):  
Qing Yun Chen ◽  
Xiao Wen Jiang
Keyword(s):  
Porous Carbon ◽  
Carbon Film ◽  
Reversible Capacity ◽  
Heat Treating ◽  
Carbon Films ◽  
X Ray Diffraction ◽  
Nickel Particles ◽  
Mesopore Structure ◽  
Graphite Structure ◽  
Li Ion

Porous carbon film was prepared from polyimide (PI) containing nickel particles by heat-treatment at different temperature. The prepared samples were investigated by multipoint brunauer-Emmett-Teller surface area (BET), scanning electron microscopy (SEM) and X-ray diffraction. The mesopore structure was obtained by heat-treating at 1000°C and the macropore and layered-graphite structure was achieved by heat-treating at 1600°C. The electrochemical properties of the carbon films were studied by galvanostatic cycling. The results showed that the reversible capacity of the carbon film treated at 1600°C is a promising material to be used in the lithium battery.

Benzylamine Tartrate as an Organic Glass Substrate for Carbon Films by Evaporation

1970 ◽  
Vol 28 ◽  
pp. 484-485
Author(s):  
A. C. Faberge
Keyword(s):  
Vapor Pressure ◽  
Viscous Liquid ◽  
Glass Substrate ◽  
Room Temperature ◽  
Carbon Film ◽  
Carbon Films ◽  
Organic Glass ◽  
Spectroscopic Examination ◽  
Polymeric Substrates

Benzylamine tartrate (m.p. 63°C) seems to be a better and more convenient substrate for making carbon films than any of those previously proposed. Using it in the manner described, it is easy consistently to make batches of specimen grids as open as 200 mesh with no broken squares, and without individual handling of the grids. Benzylamine tartrate (hereafter called B.T.) is a viscous liquid when molten, which sets to a glass. Unlike polymeric substrates it does not swell before dissolving; such swelling of the substrate seems to be a principal cause of breakage of carbon film. Mass spectroscopic examination indicates a vapor pressure less than 10−9 Torr at room temperature.

Carbon Film Deposition On Silicon Using Low Energy Ion Beams

1991 ◽  
Vol 223 ◽  
Author(s):  
Qin Fuguang ◽  
Yao Zhenyu ◽  
Ren Zhizhang ◽  
S.-T. Lee ◽  
I. Bello ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Ion Beam ◽  
Carbon Film ◽  
Carbon Films ◽  
Film Deposition ◽  
Ion Energy ◽  
Transmission Electron ◽  
Higher Temperature ◽  
Post Implantation ◽  
Beam Deposition

ABSTRACTDirect ion beam deposition of carbon films on silicon in the ion energy range of 15–500eV and temperature range of 25–800°C has been studied using mass selected C+ ions under ultrahigh vacuum. The films were characterized with X-ray photoelectron spectroscopy, Raman spectroscopy, and transmission electron microscopy and diffraction analysis. Films deposited at room temperature consist mainly of amorphous carbon. Deposition at a higher temperature, or post-implantation annealing leads to formation of microcrystalline graphite. A deposition temperature above 800°C favors the formation of microcrystalline graphite with a preferred orientation in the (0001) direction. No evidence of diamond formation was observed in these films.

Study of Transcrystallization in Polymer Composites

1989 ◽  
Vol 170 ◽  
Author(s):  
Benjamin S. Hsiao ◽  
J. H. Eric
Keyword(s):  
Thermal Conductivity ◽  
Free Energy ◽  
Carbon Fiber ◽  
Plasma Treatment ◽  
Polymer Composites ◽  
High Performance ◽  
Interfacial Strength ◽  
Fiber Surface ◽  
Semicrystalline Polymers ◽  
First Case

AbstractTranscrystallization of semicrystalline polymers, such as PEEK, PEKK and PPS, in high performance composites has been investigated. It is found that PPDT aramid fiber and pitch-based carbon fiber induce a transcrystalline interphase in all three polymers, whereas in PAN-based carbon fiber and glass fiber systems, transcrystallization occurs only under specific circumstances. Epitaxy is used to explain the surface-induced transcrystalline interphase in the first case. In the latter case, transcrystallization is probably not due to epitaxy, but may be attributed to the thermal conductivity mismatch. Plasma treatment on the fiber surface showed a negligible effect on inducing transcrystallization, implying that surface-free energy was not important. A microdebonding test was adopted to evaluate the interfacial strength between the fiber and matrix. Our preliminary results did not reveal any effect on the fiber/matrix interfacial strength of transcrystallinity.

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