Hostname: page-component-586b7cd67f-dsjbd Total loading time: 0 Render date: 2024-11-29T08:00:45.130Z Has data issue: false hasContentIssue false
  • English
  • Français

Real Time Measurement of Functional Groups Substitution on Fluorocarbon Surface by ATR FT-IR

Published online by Cambridge University Press:  01 February 2011

Yuki Sato  and
Masataka Murahara
Yuki Sato
Affiliation:
Depertment of Electrical and Electronic Engineering, Tokai University 1117. Kitakaname Hiratuka Kanagawa, 259–1292, JAPAN
Masataka Murahara
Affiliation:
Depertment of Electrical and Electronic Engineering, Tokai University 1117. Kitakaname Hiratuka Kanagawa, 259–1292, JAPAN
Get access

Abstract

The photochemical reaction process steps in substituting the functional groups on the surface of fluorocarbon [FEP] by irradiating an Xe2 excimer lamp on water or formic acid and FEP placed on the attenuated total reflectance [ATR] prism, has been measured in real time. These steps include, water photo-dissociation, the defluorination of the FEP and the hydrophilic group substitution.

In case of formic acid, the absorption peaks of the -CHO in the region of 2940 cm−1 and the -COOH in the region of 1710 cm−1 decreased respectively by photo dissociation, but that of the -OH in the region of 3300cm−1 increased. The results indicated that the -CHO and -COOH have turned to -OH.

Furthermore, the contact angle with water was measured. When compared to the untreated sample, whose contact angle was 110 degrees, the contact angle of the sample treated with water and the Xe2 lamp irradiation for 25 minutes became 31 degrees, and that of the sample modified with formic acid and the lamp irradiated for 25 minutes further improved to 17 degrees. This implies that the hydrophilic groups were produced more in formic acid than in water.

Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 843: Symposium T – Surface Engineering-Fundamentals and Applications , 2004 , T3.16
Copyright
Copyright © Materials Research Society 2005

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

1. Kurotobi, K., Kaibara, M., Suzuki, Y., Iwaki, M. and Nakajima, H., Nucl. Instr. And Meth. In Phys. Res. B175–177, 791–796 (2001).Google Scholar
2. Suzuki, Y., Takahashi, N., Iwaki, M., Ujiie, H. and Hori, T., Technology on Adhesion and Sealing of Japan 48 No.9, 393–397 (2004)Google Scholar
3. Suzuki, H., Sobue, S., Nagakubo, M. and Hattori, T., Surface Science Society of Japan 18 No.7, pp.399–404 (1997)Google Scholar
4. Park, Y. W., Tasaka, S., Inagaki, N., J. Appl. Polym. Sci. 83, 1258–1267 (2002)Google Scholar
5. Okoshi, M., Murahara, M. and Toyoda, K., J. Mater. Res. 7, 1912–1916 (1992)Google Scholar
6. Murahara, M. and Okoshi, M., J. Adhesion Sci. Technol. 9, 1593–1599 (1995)Google Scholar
7. Murahara, M. and Toyoda, K., J. Adhesion Sci. Technol. 9, 1601–1609 (1995)Google Scholar
8. Okoshi, M. and Murahara, M., App. Phys. Lett. 72, 2616–2618 (1998)Google Scholar
9. Okabe, H., Photochemistry of Small Molecules, (a Wiley Interscience, N. Y., 1978) 62–163 Google Scholar
10. Ikegame, T. and Murahara, M., Mat. Res. Soc. Symp. Proc. 544, 227–232 (1999)Google Scholar