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Adhesion Properties of Cellulose Films

Published online by Cambridge University Press:  10 February 2011

Xiujuan Zhang
Affiliation:
Materials Science Program University of Wisconsin-Madison, Madison, WI 53706
Raymond. A. Young
Affiliation:
Materials Science Program University of Wisconsin-Madison, Madison, WI 53706
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Abstract

The adhesion properties were evaluated for untreated and modified cellulose (cellophane) films. Several functional groups were introduced on the film surfaces by plasma based treatments. All the films were characterized by atomic force microscopy (AFM) and scanning electron microscopy (SEM). AFM was employed to study the adhesion properties using both standard silicon nitride tips as well as self-assembled monolayer (SAM) modified gold coated tips containing a variety of specific functional groups. The acetone extracted cellulose films, which are rich in –OH groups, were used as substrates. The adhesion force detected with –COOH terminated AFM tips (∼ 34.8 nN) was much larger than that with –CH3 terminated AFM tips (∼16.7 nN), which was attributed to the hydrogen bonding between –COOH and –OH functional groups. The adhesion force of –NH2 terminated AFM tips on the acetone extracted cellulose film was higher at 42.92 nN. However, after surface modification of the cellulose films with argon and oxygen based plasma treatments, the adhesion force were decreased to 17.4 and 19.4 nN respectively as a result of greatly enhanced surface roughness. Hydrazine plasma treatment also was used to introduce –NH2 groups on the film surfaces, and the strongest adhesion behavior was observed with AFM tips terminated with -COOH groups on the aminated film due to acid-base interaction. The argon and oxygen plasma treatment greatly increased the surface roughness, resulting in poor adhesion properties. Both surface roughness and chemical modification of the cellophane films affected the adhesion properties as measured by AFM force curves.

Type
Research Article
Copyright
Copyright © Materials Research Society 2000

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References

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