Surface Modification of Graphene Nanoparticles With Ethylene Plasma in Rotary Plasma Reactor for the Preparation of GnP/HDPE Nanocomposites

2018 ◽  
Vol 46 (7) ◽  
pp. 2402-2406 ◽  
Author(s):  
Raymundo Zendejo-Covarrubias ◽  
Rosa Idalia Narro-Cespedes ◽  
Guadalupe Neira-Velazquez ◽  
Victor J. Cruz-Delgado ◽  
J. J. Ku-Herrera ◽  
...  
1993 ◽  
Vol 49 (10) ◽  
pp. 1857-1863 ◽  
Author(s):  
A. Holländer ◽  
J. Behnisch ◽  
H. Zimmermann

Polymers ◽  
2020 ◽  
Vol 12 (12) ◽  
pp. 3020
Author(s):  
Gregor Primc

A review of the most significant scientific achievements in the field of surface modification of polyamides by non-equilibrium plasma treatments is presented. Most authors employed atmospheric pressure discharges and reported improved wettability. The super-hydrophilic surface finish was only achieved using a low-pressure plasma reactor and prolonged treatment time, enabling both the nanostructuring and functionalization with polar functional groups. The average increase of the oxygen concentration as probed by XPS was about 10 at%, while the changes in nitrogen concentrations were marginal in almost all cases. The final static water contact angle decreased with the increasing treatment time, and the oxygen concentration decreased with the increasing discharge power. The need for plasma characterization for the interpretation of experimental results is stressed.


2018 ◽  
Vol 44 (4) ◽  
pp. 236-241
Author(s):  
Nobusuke Kobayashi ◽  
Baiqiang Zhang ◽  
Kengo Hanai ◽  
Yoshinori Itaya

Polymers ◽  
2019 ◽  
Vol 11 (12) ◽  
pp. 1957 ◽  
Author(s):  
Xiaozhen He ◽  
Ilkka Rytöluoto ◽  
Rafal Anyszka ◽  
Amirhossein Mahtabani ◽  
Eetta Saarimäki ◽  
...  

Novel nanocomposites for dielectric applications-based polypropylene/poly(ethylene-co-octene) (PP/POE) blends filled with nano silica are developed in the framework of the European ‘GRIDABLE’ project. A tailor-made low-pressure-plasma reactor was applied in this study for an organic surface modification of silica. Acetylene gas was used as the monomer for plasma polymerization in order to deposit a hydrocarbon layer onto the silica surface. The aim of this modification is to increase the compatibility between silica and the PP/POE blends matrix in order to improve the dispersion of the filler in the polymer matrix and to suppress the space charge accumulation by altering the charge trapping properties of these silica/PP/POE blends composites. The conditions for the deposition of the acetylene plasma-polymer onto the silica surface were optimized by analyzing the modification in terms of weight loss by thermogravimetry (TGA). X-ray photoelectron spectroscopy (XPS) and energy-dispersive X-ray fluorescence spectroscopy (EDX) measurements confirmed the presence of hydrocarbon compounds on the silica surface after plasma modification. The acetylene plasma modified silica with the highest deposition level was selected to be incorporated into the PP/POE blends matrix. X-ray diffraction (XRD) showed that there is no new crystal phase formation in the PP/POE blends nanocomposites after addition of the acetylene plasma modified silica. Differential scanning calorimetry results (DSC) show two melting peaks and two crystallization peaks of the PP/POE blends nanocomposites corresponding to the PP and POE domains. The improved dispersion of the silica after acetylene plasma modification in the PP/POE blends matrix was shown by means of SEM–EDX mapping. Thermally stimulated depolarization current (TSDC) measurements confirm that addition of the acetylene plasma modified silica affects the charge trapping density and decreases the amount of injected charges into PP/POE blends nanocomposites. This work shows that acetylene plasma modification of the silica surface is a promising route to tune charge trapping properties of PP/POE blend-based nanocomposites.


1990 ◽  
Vol 51 (C4) ◽  
pp. C4-285-C4-290
Author(s):  
A. H. HESHMATI ◽  
A. M. EKTESSABI ◽  
Sh. SHAHNAZI ◽  
Sh. ZAMINI

1997 ◽  
Vol 67 (5) ◽  
pp. 359-369 ◽  
Author(s):  
Peter P. Tsai ◽  
Larry C. Wadsworth ◽  
J. Reece Roth

In industrial applications, a steady-state glow discharge capable of operating at one atmosphere would allow many plasma-related surface modification processes to be done on the production line, rather than in expensive vacuum systems that force batch processing. In this paper, we report some encouraging results from the plasma surface treatment of polypropylene meltblown nonwovens in the UTK one-atmosphere glow discharge plasma reactor. This reactor generates a large volume (up to 2.4 liters), low power (less than 150 watts), uniform glow discharge plasma in a parallel plate configuration with oval electrodes of 213 cm2 face area, the lower electrode being covered with a 3.2 mm thick insulating Pyrex surface. The plates are set up in an enclosed box that makes it possible to control the working gas used, and the spacing between the plates can be varied. This reactor is energized by a custom-made high impedance kilohertz power supply capable of supplying up to 5 kilowatts of kilohertz power at RMS voltages up to 10 kV, and over a frequency range from 1 to 100 kHz. Exposing a wide variety of polymer fabrics reveals that the wettability, wickability, printability, and surface contact angle of the materials are significantly changed in a direction that may lead to new uses for these materials.


Processes ◽  
2022 ◽  
Vol 10 (1) ◽  
pp. 104
Author(s):  
Panagiotis Dimitrakellis ◽  
François Faubert ◽  
Maxime Wartel ◽  
Evangelos Gogolides ◽  
Stéphane Pellerin

We studied the epoxy polymer surface modification using air plasma treatment in a Gliding Arc (GA) plasma reactor and a pulsed Dielectric Barrier Discharge (DBD). We employed optical emission spectroscopy (OES) measurements to approximate the vibrational and rotational temperatures for both plasma sources, as well as surface temperature measurements with fiber optics and IR thermography to corelate with the corresponding hydrophilization of the epoxy material. Water contact angle measurements revealed a rapid hydrophilization for both plasma sources, with a slightly more pronounced effect for the air DBD treatment. Ageing studies revealed stable hydrophilicity, with water contact angle saturating at values lower than 50°, corresponding to a >50% decrease compared to the untreated epoxy polymer. ATR-FTIR spectroscopy studies showed an additional absorption band assigned to carbonyl group, with its peak intensity being higher for the DBD treated surfaces. The spectra were also correlated with the surface functionalization via the relative peak area ratio of carbonyl to oxirane and benzene related bands. According to SEM imaging, GA plasma treatment led to no apparent morphological change, contrary to DBD treatment, which resulted in nano-roughness formation. The enhanced surface oxidation as well as the nano-roughness formation on epoxy surface with the air DBD treatment were found to be responsible for the stable hydrophilization.


1987 ◽  
Vol 108 ◽  
Author(s):  
P. M. Scott ◽  
S. V. Babu ◽  
R. E. Partch ◽  
L. J. Matienzo

ABSTRACTSome results of simultaneous measurement of polyimide etch rates, temperature, and O− and F− atom emission intensities in CF4/O2 plasma discharges are described. Several process variables have been investigated both during steady and unsteady plasma reactor operation. Atomic compositions on the polymer surface have been determined as a function of time of exposure to the plasma using ESCA, and the C IS spectra apalyzed to identify the various C-O and C-F bonds.


2021 ◽  
Vol 11 (1) ◽  
pp. 2
Author(s):  
Pieter Samyn

The classical production of microfibrillar cellulose involves intensive mechanical processing and discontinuous chemical treatment in solvent-based media in order to introduce additional chemical surface modification. By selecting appropriate conditions of a pulsed plasma reactor, a solvent-free and low-energy input process can be applied with the introduction of microcrystalline cellulose (MCC) and maleic anhydride (MA) powders. The plasma processing results in the progressive fibrillation of the cellulose powder into its elementary fibril structure and in-situ modification of the produced fibrils with more hydrophobic groups that provide good stability against re-agglomeration of the fibrils. The selection of a critical ratio MA/MCC = 2:1 allows separating the single cellulose microfibrils with changeable morphologies depending on the plasma treatment time. Moreover, the density of the hydrophobic surface groups can be changed through a selection of different plasma duty cycle times, while the influence of plasma power and pulse frequency is inferior. The variations in treatment time can be followed along the plasma reactor, as the microfibrils gain smaller diameter and become somewhat longer with increasing time. This can be related to the activation of the hierarchical cellulose structure and progressive diffusion of the MA within the cellulose structure, causing progressive weakening of the hydroxyl bonding. In parallel, the creation of more reactive species with time allows creating active surface sites that allow for interaction between the different fibrils into more complex morphologies. The in-situ surface modification has been demonstrated by XPS and FTIR analysis, indicating the successful esterification between the MA and hydroxyl groups at the cellulose surface. In particular, the crystallinity of the cellulose has been augmented after plasma modification. Furthermore, AFM evaluation of the fibrils shows surface structures with irregular surface roughness patterns that contribute to better interaction of the microfibrils after incorporation in an eventual polymer matrix. In conclusion, the combination of physical and chemical processing of cellulose microfibrils provides a more sustainable approach for the fabrication of advanced nanotechnological materials.


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