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Simulations of the Structure and Properties of the Polyethylene Crystal Surface

Published online by Cambridge University Press:  10 February 2011

J. L. Wilhelmi  and
G. C. Rutledge
J. L. Wilhelmi
Affiliation:
Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139
G. C. Rutledge
Affiliation:
Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139
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Abstract

The structures and thermodynamic properties of the (100), (010), and (110) lateral surfaces of extended-chain polyethylene crystals between 0 K and 300 K were determined by free energy minimization using consistent quasi-harmonic lattice dynamics. Slight rotations of the outermost chains from their corresponding orientations in the bulk were observed. These deviations from bulk structure were confined to the first three molecular layers (approximately 10 Å) at the surface. Surface free energy calculations found the (110) surface to be the most stable over the entire temperature range modeled, with free energies ranging from 95.4 erg/cm2 to 103.5 erg/cm2, at temperatures of 0 K and 300 K, respectively. Surface free energies of the (100) and (010) surfaces were found to be at least 15% higher than the (110) surface, with the (100) surface slightly more stable than the (010) surface, over all temperatures considered. Surface free energy increases as the density of chains at the surface decreases. The surface free energy at low temperatures was determined predominantly by intermolecular potential energy; at higher temperatures, excess entropy accounted for nearly half the surface free energy. Surface entropy was almost entirely due to lattice mode motions.

Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 408: Symposium P – Materials Theory, Simulations, and Parallel Algorithms , 1995 , 469
Copyright
Copyright © Materials Research Society 1996

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References

1. Lauritzen, J. and Hoffman, J., J. Research NBS, 1960, 64A, 73.Google Scholar
2. Karasawa, N., Dasgupta, S. and Goddard, W., J. Phys. Chem., 1991, 95, 2260.Google Scholar
3. Yamamoto, T., Hikosaka, M. and Takahashi, N., Macromolecules, 1994, 27, 1466.Google Scholar
4. Liang, G., Noid, D., Sumpter, B. and Wunderlich, B., Makromol. Chem., Theory Simul., 1993, 2, 245.Google Scholar
5. Lacks, D. and Rutledge, G.C., J. Phys. Chem., 1994, 98, 1231.Google Scholar
6. Willis, B. and Pryor, A., Thermal Vibrations in Crystallography, Cambridge University Press, London, 1975, pp. 1–77.Google Scholar
7. Lutsko, J., Wolf, D. and Yip, S., J. Chem. Phys., 1988, 88, 6525.Google Scholar
8. Lacks, D. and Rutledge, G.C., J. Chem. Phys., 1994, 101, 9961.Google Scholar
9. de Wette, F.W., in Interatomic Potentials and Simulation of Lattice Defects, Plenum, New York, 1972, pp. 653–671.Google Scholar
10. Thomas, D. and Staveley, L.,J. of Chem. Soc.,1952, 4569.Google Scholar