Hostname: page-component-77c89778f8-cnmwb Total loading time: 0 Render date: 2024-07-21T03:35:57.313Z Has data issue: false hasContentIssue false

Correlation of Structure and Mechanical Properties of Polyolefin Surfaces by Ir + Visible Sum Frequency Generation Vibrational Spectroscopy and Atomic Force Microscopy

Published online by Cambridge University Press:  10 February 2011

D. H. Gracias
Affiliation:
Department of Chemistry, University of California at Berkeley, CA 94720 Lawrence Berkeley National Laboratory, Berkeley, CA 94720
D. Zhang
Affiliation:
Department of Chemistry, University of California at Berkeley, CA 94720 Lawrence Berkeley National Laboratory, Berkeley, CA 94720
Y. R. Shen
Affiliation:
Department of Physics, University of California at Berkeley, CA 94720 Lawrence Berkeley National Laboratory, Berkeley, CA 94720
G. A. Somorjai
Affiliation:
Department of Chemistry, University of California at Berkeley, CA 94720 Lawrence Berkeley National Laboratory, Berkeley, CA 94720
Get access

Abstract

The surface vibrational spectrum of atactic polypropylene was measured using IR+Visible Sum Frequency Generation (SFG) vibrational spectroscopy, in the temperature range 23 to -50 °C. A sharp rise in the intensity of the C-H symmetric stretch of CH2 groups is observed in the temperature range 0 to -20 °C . The elastic modulus and friction of the same polymer were measured with Atomic Force Microscopy (AFM) in the same temperature range i.e. 23 to -50 °C. There is a sharp rise in the modulus and a sharp decrease in the friction coefficient, at temperatures between 23 and 0 °C. These changes are attributed to the glass transition in atactic polypropylene which is expected to occur in the temperature range 10 to -10 °C. The temperature at which the glass transition is observed, from changes detected in AFM experiments, is higher than that observed by SFG experiments and that expected from bulk measurements. This elevation in the glass transition temperature has been attributed to the high pressure applied to the polymer under the AFM tip.

Type
Research Article
Copyright
Copyright © Materials Research Society 1998

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

(1) Zhang, D., Shen, Y.R., and Somorjai, G.A., Chemical Physics Letters 281, p. 394 (1998).Google Scholar
(2) Gracias, D.H. and Somorjai, G.A., Macromolecules 31, p. 12 69 (1998).Google Scholar
(3) Bogdanov, B.G. and Michailov, M. Handbook of Polyolefins, edited by Vasile, C., and Seymour, R., Marcel Dekker, New York, 1993; p 368 Google Scholar
(4) Frohn, J., Wolf, J.F., Besocke, K. and Teske, M., Rev. Sci. Instrum. 60, p.1200 (1989)Google Scholar
(5) NT-MDT Co., Moscow, Russia.Google Scholar
(6) Johnson, K.L. Contact Mechanics, 1st ed.; Cambridge University Press, New York, 1987; p 84105.Google Scholar
(7) Mears, D., Pae, K., and Sauer, J.A., J of Appl. Phys. 40, p. 4229 (1969)Google Scholar