Sensing Polymer Chain Dynamics through Ring Topology: A Neutron Spin Echo Study

被引:47
作者
Goossen, Sebastian [1 ,2 ]
Krutyeva, Margarita [1 ,2 ]
Sharp, Melissa [3 ,4 ]
Feoktystov, Artem [5 ]
Allgaier, Juergen [1 ,2 ]
Pyckhout-Hintzen, Wim [1 ,2 ]
Wischnewski, Andreas [1 ,2 ]
Richter, Dieter [1 ,2 ]
机构
[1] Forschungszentrum Julich, Julich Ctr Neutron Sci JCNS 1, D-52425 Julich, Germany
[2] Forschungszentrum Julich, Inst Complex Syst ICS 1, D-52425 Julich, Germany
[3] ILL Grenoble, F-38042 Grenoble 9, France
[4] European Spallat Source ESS AB, S-22100 Lund, Sweden
[5] Forschungszentrum Julich, JCNS, Heinz Maier Leibnitz Zentrum MLZ, D-85747 Garching, Germany
关键词
CONTOUR-LENGTH FLUCTUATIONS; CYCLIC POLYMERS; POLY(ETHYLENE OXIDE); ENTANGLED POLYMERS; LINEAR-POLYMERS; MELTS; DIFFUSION; RELAXATION; STRATEGIES; MOLECULES;
D O I
10.1103/PhysRevLett.115.148302
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
Using neutron spin echo spectroscopy, we show that the segmental dynamics of polymer rings immersed in linear chains is completely controlled by the host. This transforms rings into ideal probes for studying the entanglement dynamics of the embedding matrix. As a consequence of the unique ring topology, in long chain matrices the entanglement spacing is directly revealed, unaffected by local reptation of the host molecules beyond this distance. In shorter entangled matrices, where in the time frame of the experiment secondary effects such as contour length fluctuations or constraint release could play a role, the ring motion reveals that the contour length fluctuation is weaker than assumed in state-of-the-art rheology and that the constraint release is negligible. We expect that rings, as topological probes, will also grant direct access to molecular aspects of polymer motion which have been inaccessible until now within chains adhering to more complex architectures.
引用
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页数:5
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