ToF-SIMS observation of PTFE surfaces modified by α-particle irradiation

The surface structure of polytetrafluoroethylene (PTFE) upon α‐particle irradiation has been investigated at doses in the range of 1 × 107 to 1 × 1011 Rad and compared with the surface structure of the unirradiated polymer. Both neat and 25% fiberglass content PTFE were studied. The samples, maintai...

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Published in:Surface and interface analysis Vol. 37; no. 9; pp. 713 - 720
Main Authors: Fisher, Gregory L., Ohlhausen, James A., Wetteland, Christopher J.
Format: Journal Article
Language:English
Published: Chichester, UK John Wiley & Sons, Ltd 01-09-2005
Wiley
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Summary:The surface structure of polytetrafluoroethylene (PTFE) upon α‐particle irradiation has been investigated at doses in the range of 1 × 107 to 1 × 1011 Rad and compared with the surface structure of the unirradiated polymer. Both neat and 25% fiberglass content PTFE were studied. The samples, maintained at nominal room temperature, were irradiated in vacuum by 5.5 MeV 4He2+ ions generated in a tandem accelerator beam line. Static time‐of‐flight SIMS (ToF‐SIMS) was employed to probe chemical changes at the surface as a function of the irradiation level. In general, the data are indicative of increased cross‐linking at α‐doses less than 1 × 109 Rad, followed by increased fragmentation and unsaturation at α‐doses greater than 1 × 109 Rad. Throughout the irradiation regime, scission is a constant factor promoting cross‐linking, branching, and unsaturation. However, at α‐doses greater than 1 × 1010 Rad, extreme structural degradation of the polymer becomes evident and is accompanied by conversion to oxygen‐functionalized and aliphatic compounds. Thus, for PTFE in an α‐particle field, an upper exposure limit of ∼1010 Rad is essential for nominal retention of molecular structure. Finally, a quantitative relationship between α‐dose and characteristic fragment ion intensity is developed. Copyright © 2005 John Wiley & Sons, Ltd.
Bibliography:ArticleID:SIA2068
United States Department of Energy - No. W-7405-ENG.
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ObjectType-Article-2
SourceType-Scholarly Journals-1
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content type line 23
ISSN:0142-2421
1096-9918
DOI:10.1002/sia.2068