Abstract

Defluorination of polytetrafluoroethylene (PTFE) surface film is a suitable technique for tailoring its surface properties. The influence of discharge parameters on the surface chemistry was investigated systematically using radio-frequency inductively coupled H2 plasma sustained in the E- and H-modes at various powers, pressures and treatment times. The surface finish was probed by X-ray photoelectron spectroscopy (XPS) and time-of-flight secondary ion mass spectrometry (ToF-SIMS). The measurements of water contact angles (WCA) showed increased wettability of the pristine PTFE; however, they did not reveal remarkable modification in the surface chemistry of the samples treated at various discharge parameters. By contrast, the combination of XPS and ToF-SIMS, however, revealed important differences in the surface chemistry between the E- and H-modes. A well-expressed minimum in the fluorine to carbon ratio F/C as low as 0.2 was observed at the treatment time as short as 1 s when plasma was in the H-mode. More gradual surface chemistry was observed when plasma was in the E-mode, and the minimal achievable F/C ratio was about 0.6. The results were explained by the synergistic effects of hydrogen atoms and vacuum ultraviolet radiation.

Highlights

  • Fluorinated polymers are used in various applications [1]

  • The samples treated within the coil assume the water contact angles (WCA) of approximately 83°, which is the value already reported by previously cited authors

  • This value is typical for oxygen-free polymers such as polyolefins. Such a rather low WCA extends a few cm away from the coil, which is explained by the simple fact that a dense plasma in the H-mode was not limited to the coil only, but PTFE samples upon treatment with a dense, glowing hydrogen plasma, and a more gradual activation upon treatment with a diffusing plasma, which in our case is a result of a weak capacitive coupling between the coil and the metallic pump duct

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Summary

Introduction

Fluorinated polymers are used in various applications [1]. They are renowned for their chemical inertness and thermal stability [2]. The chemical inertness does not allow for reasonable adhesion of any coating deposited by numerous techniques [3,4]. The surface energy of the coating is much larger than the energy of the substrate; thin films tend to form 3D particles spontaneously rather than a uniform film. In order to improve the adhesion of coatings, methods for increasing the surface energy of fluorinated polymers have been invented [5,6,7,8,9,10]. Fluorinated polymers are usually treated with aggressive chemicals which

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