Plasma Treatment of Polymers for Improving Al Adhesion

1998 ◽  
Vol 544 ◽  
Author(s):  
R. Lamendola ◽  
E. Matarrese ◽  
M. Creatore ◽  
P. Favia ◽  
R. d'Agostino

AbstractPET and Kapton thin films have been plasma processed in order to increase sputtered aluminum adhesion. The effect of different plasma feedings, such as NH3, O2, and He, has been evaluated on polymer/metal adhesion and on chemical modifications of polymer surface at different plasma power and treatment time. The chemistry at polymer/metal interface has been studied in order to find the suitable experimental conditions for transferring the plasma process to industrial scale.The role of acid-base reactions in promoting Polymer/Aluminum adhesion has been investigated. Surface composition has been investigated by X-ray Photoelectron Spectroscopy; adhesion measurements have been accomplished by 180° Peel Test.

Polymers ◽  
2020 ◽  
Vol 12 (9) ◽  
pp. 2099
Author(s):  
Hana Šourková ◽  
Petr Špatenka

Polyethylene powder of average particle diameter of 160 µm was activated in a plasma reactor made from aluminum of volume 64 dm3 at the pressure 100 Pa. Dense oxygen plasma was sustained with a microwave discharge powered by a pulsed magnetron source of power 1 kW mounted onto the top flange of the plasma reactor. Polymer powder was treated in a batch mode with 0.25 kg/batch. The powder was placed into a stainless-steel dish mounted in the center of the reactor where diffusing plasma of low ion density, and the O-atom density of 2 × 1021 m−3 was sustained. The powder was stirred in the dish at the rate of 40 rpm. The evolution of powder wettability versus treatment time was measured using the Washburne method, and the surface composition was determined by X-ray Photoelectron Spectroscopy (XPS). The wettability versus the oxygen concentration assumed a parabolic behavior. The maximal oxygen concentration, as revealed by XPS, was 17.5 at.%, and the maximal increase of wettability was 220%. The efficiency of O-atoms utilization in these experimental conditions was about 10% taking into account the spherical geometry of dust particles and perfectly smooth surface. The method is scalable to large industrial systems.


Coatings ◽  
2020 ◽  
Vol 10 (11) ◽  
pp. 1067 ◽  
Author(s):  
Aya E. Abusrafa ◽  
Salma Habib ◽  
Anton Popelka

Herein, the surface treatment of polyurethane (PU) films via air, O2, N2, Ar, and their mixtures were tested. The treatment was performed to incorporate new polar functionalities on the polymer surface and achieve improved hydrophilic characteristics. The PU films were subjected to RF low-temperature plasma treatment. It was found that plasma treatment immensely enhanced the hydrophilic surface properties of the PU films in comparison with those of the pristine samples; the maximum plasma effect occurred for the PU sample in the presence of air plasma with treatment time of 180 s at nominal power of 80 W. The surface topography was also found to vary with plasma exposure time and the type of gas being used due to the reactivity of the gaseous media. Roughness analysis revealed that at higher treatment times, the etching/degradation of the surface became more pronounced. Surface chemistry studies revealed increased O2 and N2 elemental groups on the surface upon exposure to O2, N2, air, and Ar. Additionally, the aging study revealed that samples treated in the presence of air and Ar were more stable in comparison to those of the other gases for both the contact angle and peel test measurements.


1987 ◽  
Vol 2 (1) ◽  
pp. 117-131 ◽  
Author(s):  
Thomas J. Hook ◽  
Joseph A. Gardella ◽  
Lawrence Salvati

Results from x-ray photoelectron spectroscopy (XPS or ESCA), low-energy ion scattering spectrometry (LEIS or ISS); and Fourier transform infrared spectroscopy (FTIR) analyses are presented for unmodified and modified poly (methylmethacrylate) (PMMA) polymer films. Analysis of the unmodified PMMA polymers (isotactic, syndiotactic, and atactic) via ESCA, ISS, and FTIR, established the surface composition, bonding, and functionality before the modification was employed. An rf-plasma glow discharge created from an Ar/H2O gas mixture at different exposure times and power levels was used to treat the polymer surface. Subsequent ESCA, ISS, and FTIR analyses of these modified PMMA's show the effects of surface modification in terms of a model of structural differences, over a limited depth (50–100 Å). The composition and functionality changes of the resulting surfaces are discussed with respect to proposed mechanisms of the plasma reaction and differences in tacticity of the reactant. A two-step reaction mechanism involving reactive decarboxylation/reduction followed by H2O adsorption is proposed to understand the spectroscopic results.


2005 ◽  
Vol 871 ◽  
Author(s):  
K. Demirkan ◽  
A. Mathew ◽  
R. L. Opila

AbstractAl was thermally evaporated onto the conjugated semiconductor polymer, poly(2-methoxy-5,2′- ethyl-hexyloxy-phenylene vinylene) (MEH-PPV) in successive steps. Interface formation and chemical interactions between the polymer and Al were investigated by X-ray Photoelectron Spectroscopy (XPS) and synchrotron source Ultraviolet Photoelectron Spectroscopy (UPS). XPS analyses (angle resolved and sputtering depth profile) proved the formation of an insulating aluminum oxide layer at the polymer metal interface. The C-O bonds in the polymer decreased as more Al was evaporated on the MEH-PPV. Also reaction between Al and the carbon backbone of the polymer leading to the creation of carbon-metal bonds was observed. UPS analysis suggested the possibility of Al reacting with the phenylene ring of the polymer.


Nanomaterials ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 567
Author(s):  
Josef Zemek ◽  
Petr Jiricek ◽  
Jana Houdkova ◽  
Martin Ledinsky ◽  
Miroslav Jelinek ◽  
...  

This work attempts to understand the behaviour of Ge-induced cytotoxicity of germanium-doped hydrogen-free diamond-like carbon (DLC) films recently thoroughly studied and published by Jelinek et al. At a low doping level, the films showed no cytotoxicity, while at a higher doping level, the films were found to exhibit medium to high cytotoxicity. We demonstrate, using surface-sensitive methods—two-angle X-ray-induced core-level photoelectron spectroscopy (ARXPS) and Low Energy Ion Scattering (LEIS) spectroscopy, that at a low doping level, the layers are capped by a carbon film which impedes the contact of Ge species with tissue. For higher Ge content in the DLC films, oxidized Ge species are located at the top surface of the layers, provoking cytotoxicity. The present results indicate no threshold for Ge concentration in cell culture substrate to avoid a severe toxic reaction.


2017 ◽  
Vol 62 (2) ◽  
pp. 1205-1208 ◽  
Author(s):  
G. Szabó

AbstractIn this study the major topic were the bonding properties of the layer-clad aluminum sheets. The bonding was performed between AlMn1Si0.8 and AlSi10 alloys using hot rolling (a VON ROLL experimental duo mill). The experimental temperatures were 460, 480 and 500°C. The goodness of bonding was tested by tensile test and T-peel test. T-peel test provided a good description about the quality of bonding. Structure analysis was also performed by light microscopy to detect typical bonding faults. The aim of this investigation is modelling the bonding conformation in experimental conditions. Further aim of this investigation is to produce some typical bonding faults and find the cause of formation. The influence of the rolling temperature and surface roughness on the bonding was also analyzed. Rolling schedule and the role of first pass on the development of perfect bonding were experimentally determined.


MRS Bulletin ◽  
1996 ◽  
Vol 21 (1) ◽  
pp. 43-48 ◽  
Author(s):  
Hengzhong Zhuang ◽  
Joseph A. Gardella

The surface science of polymer materials has recently grown to a dynamic field, largely because of application in such areas as composite materials, wetting, coatings, adhesion, friction, and biocompatibility. The synthesis of new polymer materials, resulting in desired polymer-surface structures and composition, has become more sophisticated and is driving the development of new spectroscopic probes and continuing evolution of more established methods.A good example of how instrumentation development has led to better applications in polymer-surface science is to follow the growth of studies using x-ray photoelectron spectroscopy (XPS)—also called electron spectroscopy for chemical analysis (ESCA). ESCA is now routinely used to obtain surface composition of polymers, and to follow processing steps and degradation chemistry. Advances in instrumentation have driven many of these more sophisticated applications.Nevertheless, to improve the understanding of polymer-surface chemistry, more information is needed about surface structure with further sophistication, at a higher level of precision. For example, the knowledge of orientation and subsequent reactive availability of functional groups and of monomer ar rangement along a chain in copolymers and intrachain interactions is important. Macromolecular chain arrangement, termination, branching, and micromorphological information (i.e., domain size and distribution), molecular-weight distributions at or near the surface (in comparison with the average, bulk distribution), and higher degrees of spatial resolution in all three dimensions are all important in determining sophisticated surface structure-property relationships. To approach this level of structural and reactivity information at surfaces and interfaces, evolution of established methods and development of new methods must both be accomplished.


Author(s):  
Nalin J. Unakar

The increased number of lysosomes as well as the close approximation of lysosomes to the Golgi apparatus in tissue under variety of experimental conditions is commonly observed. These observations suggest Golgi involvement in lysosomal production. The role of the Golgi apparatus in the production of lysosomes in mouse liver was studied by electron microscopy of liver following toxic injury by CCI4.


Author(s):  
M.P. Thomas ◽  
A.R. Waugh ◽  
M.J. Southon ◽  
Brian Ralph

It is well known that ion-induced sputtering from numerous multicomponent targets results in marked changes in surface composition (1). Preferential removal of one component results in surface enrichment in the less easily removed species. In this investigation, a time-of-flight atom-probe field-ion microscope A.P. together with X-ray photoelectron spectroscopy XPS have been used to monitor alterations in surface composition of Ni3Al single crystals under argon ion bombardment. The A.P. has been chosen for this investigation because of its ability using field evaporation to depth profile through a sputtered surface without the need for further ion sputtering. Incident ion energy and ion dose have been selected to reflect conditions widely used in surface analytical techniques for cleaning and depth-profiling of samples, typically 3keV and 1018 - 1020 ion m-2.


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