Self-Diffusion and Cooperative Diffusion in Semidilute Polymer Solutions As Measured by Fluorescence Correlation Spectroscopy

被引:85
|
作者
Zettl, Ute [2 ]
Hoffmann, Sebastian T. [2 ]
Koberling, Felix [4 ]
Krausch, Georg [3 ]
Enderlein, Joerg [5 ]
Harnau, Ludger [6 ,7 ]
Ballauff, Matthias [1 ]
机构
[1] Helmholtz Zentrum Berlin, Soft Matter & Funct Mat, D-14109 Berlin, Germany
[2] Univ Bayreuth, D-95440 Bayreuth, Germany
[3] Johannes Gutenberg Univ Mainz, Mainz, Germany
[4] Picoquant GmbH, D-12489 Berlin, Germany
[5] Univ Gottingen, Inst Phys, D-37077 Gottingen, Germany
[6] Max Planck Inst Met Res, D-70569 Stuttgart, Germany
[7] Univ Stuttgart, Inst Theoret & Angew Phys, D-70569 Stuttgart, Germany
关键词
DYNAMIC LIGHT-SCATTERING; MODE-COUPLING THEORY; RELAXATION-TIME DISTRIBUTIONS; MOLECULAR-WEIGHT DEPENDENCE; INTEGRAL-EQUATION THEORY; CONCENTRATION FLUCTUATIONS; MUTUAL-DIFFUSION; GOOD SOLVENT; LINEAR-POLYMERS; DILUTE-SOLUTION;
D O I
10.1021/ma901404g
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
We present a comprehensive investigation of polymer diffusion in the semidilute regime by fluorescence correlation spectroscopy (FCS) and dynamic light scattering (DLS). Using single-labeled polystyrene chains, FCS leads to the self-diffusion coefficient while DLS gives the cooperative diffusion coefficient for exactly the same molecular weights and concentrations. Using FCS we observe a new Fast mode in the semidilute entangled concentration regime beyond the slower mode which is due to self-diffusion. Comparison of FCS data with data obtained by DLS oil the same polymers shows that the second mode observed in FCS is identical to the cooperative diffusion coefficient Measured with DLS. Ail in-depth analysis and a comparison with current theoretical models demonstrates that the new cooperative mode observed in FCS is due to the effective long-range interaction of the chains through the transient entanglement network.
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页码:9537 / 9547
页数:11
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