Abstract:The active screen plasma system has been extensively studied over the past few years, mainly for plasma nitriding purposes. This technique also provides possibilities of treating non-electrical conducting materials, such as polymeric ones, which is unattainable with a conventional DC plasma system. In this work, an active screen plasma setup for maleic anhydride (MA) film deposition on a glass substrate was used. The plasma working gas was a mixture of argon and MA vapour. Films obtained through conventional p… Show more
“…Maleic anhydride (MA) is a multifunctional and biocompatible polymer that can be deposited by plasma polymerization [ 12 ]. In order to maximize the retention of functional groups in plasma-polymerized p(MA) films, a critical balance of plasma parameters should be selected with low nominal power or low pulsing times [ 13 , 14 , 15 ]. The film formation is governed by gas-phase dissociation and growth processes, which need to be narrowly controlled in parallel with complex interactions in the plasma reactor [ 16 , 17 ].…”
The creation of novel surface morphologies through thin-film patterning is important from a scientific and technological viewpoint in order to control specific surface properties. The pulsed-plasma polymerization of thin nanocomposite films, including maleic anhydride (MA) and cellulose nanocrystals (CNC), may result in different metastable film morphologies that are difficult to control. Alternatively, the transformation of deposited plasma films into crystalline structures introduces unique and more stable morphologies. In this study, the structural rearrangements of plasma-polymerized (MA+CNC) nanocomposite films after controlled hydrolysis in a humid atmosphere were studied, including effects of plasma conditions (low duty cycle, variable power) and monomer composition (ratio MA/CNC) on hydrolysis stability. The progressive growth of crystalline structures with fractal dendrites was observed in confined thin films of 30 to 50 nm. The structures particularly formed on hydrophilic substrates and were not observed before on the more hydrophobic substrates, as they exist as a result of water penetration and interactions at the film/substrate interface. Furthermore, the nucleating effect and local pinning of the crystallites to the substrate near CNC positions enhanced the film stability. The chemical structures after hydrolysis were further examined through XPS, indicating esterification between the MA carboxylic acid groups and CNC surface. The hydrolysis kinetics were quantified from the conversion of anhydride groups into carboxylic moieties by FTIR analysis, indicating enhanced hydrolytic stability of p(MA+CNC) nanocomposite films relative to the pure p(MA) films.
“…Maleic anhydride (MA) is a multifunctional and biocompatible polymer that can be deposited by plasma polymerization [ 12 ]. In order to maximize the retention of functional groups in plasma-polymerized p(MA) films, a critical balance of plasma parameters should be selected with low nominal power or low pulsing times [ 13 , 14 , 15 ]. The film formation is governed by gas-phase dissociation and growth processes, which need to be narrowly controlled in parallel with complex interactions in the plasma reactor [ 16 , 17 ].…”
The creation of novel surface morphologies through thin-film patterning is important from a scientific and technological viewpoint in order to control specific surface properties. The pulsed-plasma polymerization of thin nanocomposite films, including maleic anhydride (MA) and cellulose nanocrystals (CNC), may result in different metastable film morphologies that are difficult to control. Alternatively, the transformation of deposited plasma films into crystalline structures introduces unique and more stable morphologies. In this study, the structural rearrangements of plasma-polymerized (MA+CNC) nanocomposite films after controlled hydrolysis in a humid atmosphere were studied, including effects of plasma conditions (low duty cycle, variable power) and monomer composition (ratio MA/CNC) on hydrolysis stability. The progressive growth of crystalline structures with fractal dendrites was observed in confined thin films of 30 to 50 nm. The structures particularly formed on hydrophilic substrates and were not observed before on the more hydrophobic substrates, as they exist as a result of water penetration and interactions at the film/substrate interface. Furthermore, the nucleating effect and local pinning of the crystallites to the substrate near CNC positions enhanced the film stability. The chemical structures after hydrolysis were further examined through XPS, indicating esterification between the MA carboxylic acid groups and CNC surface. The hydrolysis kinetics were quantified from the conversion of anhydride groups into carboxylic moieties by FTIR analysis, indicating enhanced hydrolytic stability of p(MA+CNC) nanocomposite films relative to the pure p(MA) films.
“…The pulsed plasma polymerization of three different precursors (acetylene [Ac], acrylic acid [AA], maleic anhydride [MA]) was shown to be a promising method, and the chemical retention depends on the plasma chamber. [3,4,[18][19][20][21][22][23] Their corresponding plasma polymers adhered onto various substrates, mostly metallic ones for the pp-Ac [24][25][26] and polymeric ones for the other two precursors. [27,28] Therefore, here, the study was extended to other plasma parameters alone or combined (pulsed or continuous wave at different discharge powers, durations, etc.)…”
Four model plasma coatings obtained with selected parameters and precursors (acetylene, acrylic acid, and maleic anhydride) were developed for the preparation of adhesive joints of a metal/elastomer assembly. One of these layers, pulsed wave (PW), is thin and highly functionalized, while another continuous wave (CW) coated with the same thickness is less functionalized but crosslinked. The other two layers (CW × 2, CW + PW), twice as thick compared with PW and CW, show the same chemical criteria. The adhesion strength of prepared assemblies is increasing, but mostly depends on the precursor type. Moreover, such model layers allow to study the adhesion mechanism between the metal and the elastomer. The thermodynamic adhesion, that is, surface energy closer to the elastomer one, appears to prevail.
“…Plasma deposition procedure is a promising technique that can be used to supply thin films, aiming at applications such as magnetron sputtering, [ 2,3,6,10,12,18,35–37 ] hollow cathode, [ 41,42 ] active screen, [ 43–45 ] and plasma electrolytic. [ 37,46–50 ] The cathodic cage deposition process has been used for the deposition of thin films with improved physical–chemical properties with well‐defined compositions such as iron nitride, [ 51–53 ] titanium nitride, [ 54–57 ] titanium oxide, [ 58 ] copper oxide, [ 59–61 ] and molybdenum nitride.…”
Herein, the use of Hastelloy C-276 as a cathodic cage for the deposition of thin films on the AISI 316L steel substrate by plasma is investigated. The films are processed through floating potential at 350, 375, 400, and 425 C for 4 h, using a hydrogen-nitrogen mixture in the proportion of 40% and 60%, respectively. The thin films are investigated by X-ray diffraction, scanning electron microscopy, Raman spectroscopy, and potentiodynamic polarization. The spectroscopy results point out the formation of different phases such as FeNi 3 , CrNi, and MoN 1/2 . Films acquired at 375 ºC present superior corrosion resistance with less negative corrosion potential (À0.020 V). The increase and decrease in FeNi 3 and CrNi contents follow the improvement of the applied temperature, which is unbeneficial to the corrosion resistance of the films.
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