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Collapse of Isolated Chains in a Network

Published online by Cambridge University Press:  22 February 2011

R. M. Briber
Affiliation:
Department of Materials and Nuclear Engineering University of Maryland, College Park, MD 20742
X. Liu
Affiliation:
Department of Materials and Nuclear Engineering University of Maryland, College Park, MD 20742
B.J. Bauer
Affiliation:
Polymer Division, National Institute of Standard and Technology, Gaithersburg, MD 20899
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Abstract

In this study we use small angle neutron scattering to investigate the conformation of linear deuterated polystyrene chains trapped in a crosslinked protonated polystyrene matrix. The second virial coefficient was obtained as a function of crosslink density for a wide range of crosslink density. It is shown that the second virial coefficient decreases with increasing crosslink density. By extrapolating the scattering to zero concentration of the linear chain at all values of q, the single chain scattering was obtained and radius of gyration was measured the function of network density. It was found that when the network density is low (NI < Nc where NI and Nc are the number of monomer units in the linear chain and the monomer units between crosslinks, respectively) the radius of gyration does not change. As the network density increases (NI > Nc ) radius of gyration decreases. In this region the inverse of the radius of gyration varies linearly with the inverse of Nc. When the crosslink density is very high (NI » Nc ), segregation of linear polymer chains occurs. These results are in agreement with prediction and computer simulation results of polymer chain conformation in a field of random obstacles where the crosslink junctions act as the effective obstacles.

Type
Research Article
Copyright
Copyright © Materials Research Society 1995

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References

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