4.7 Article

Activation of poly(ethylene terephthalate) surfaces by atmospheric pressure plasma

Journal

POLYMER DEGRADATION AND STABILITY
Volume 97, Issue 11, Pages 2249-2254

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.polymdegradstab.2012.08.001

Keywords

Poly(ethylene terephthalate) PET; Atmospheric plasma treatment; Diffuse plasma; Polymer surface; Water contact angle; XPS

Funding

  1. Slovak Research and Development Agency [APVV-0491-07]
  2. European Development Fund
  3. Agency for Science, Technology and Research (A*STAR) of Singapore under the SERC Nanofabrication, Processing and Characterisation (SnFPC) Initiative
  4. R&D center for low-cost plasma and nanotechnology surface modifications [CZ.1.05/2.1.00/03.0086]

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We report a study on effects of atmospheric pressure plasma treatment of poly(ethylene terephthalate) PET surfaces. The atmospheric pressure plasma was generated using Diffuse Coplanar Surface Barrier Discharge (DCSBD) in ambient air. The changes in wettability of PET surfaces were studied by water contact angle measurement. The surface energy was calculated using van Oss-Chaudhury-Good model from contact angles of water, ethylene and diiodomethane. The changes in surface chemistry after the plasma treatment were studied by X-ray photoelectron spectroscopy (XPS). We also observed changes in surface roughness investigated by Atomic force microscopy (AFM). We found that DCSBD plasma treatment for 1 s led to decrease of water contact angle from 78.4 degrees to 40.1 degrees. The surface energy analysis showed that water contact angle decrease is related to increase of polar part of surface energy. XPS measurement confirmed that the plasma treatment led to increase of polar groups on PET surface which explained the changes in surface energy. AFM investigation showed that plasma treatment led to an increase of surface roughness, which could be a benefit for further processing of PET, because higher roughness increases surface area, which can result into higher adhesion between PET and coatings. (C) 2012 Elsevier Ltd. All rights reserved.

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