The behavior of the α-relaxation process in phenylphthalein–dimethylether (PDE) under high pressure was studied by means of dynamic light scattering–photon correlation spectroscopy (DLS-PCS). The temperature dependence of the relaxation time of the α-process at ambient pressure was found to resemble that obtained from dielectric relaxation (DR) measurements. On the basis of the DLS measurements one can conclude that PDE satisfies the correlation between nonexponentiality and fragility established for low-molecular weight glass forming liquids and polymers. On the other hand, dielectric relaxation studies indicate that PDE is an exception from this correlation. These differences between the DLS and DR studies do not result from the overlap of the α- and β-processes in the DLS experiments but might be due to the different coupling of the probes seen in these experiments (optical anisotropy and dipole moment) to the dynamics of the entire PDE molecule. We also studied the effect of pressure on fragility and the glass transition temperature in PDE and we found that fragility is practically independent of pressure.
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1 August 2002
Research Article|
August 01 2002
Dynamic light scattering studies of supercooled phenylphthalein–dimethylether dynamics under high pressure
Adam Patkowski;
Adam Patkowski
Institute of Physics, A Mickiewicz University, Umultowska 85, 61-614 Poznan, Poland
Max-Planck-Institut für Polymerforschung, Ackermannweg 10, 55128 Mainz, Germany
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Marian Paluch;
Marian Paluch
Institute of Physics, University of Silesia, Uniwersytecka 4, 40-007 Katowice, Poland
Max-Planck-Institut für Polymerforschung, Ackermannweg 10, 55128 Mainz, Germany
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Hartmut Kriegs
Hartmut Kriegs
Max-Planck-Institut für Polymerforschung, Ackermannweg 10, 55128 Mainz, Germany
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J. Chem. Phys. 117, 2192–2198 (2002)
Article history
Received:
October 30 2001
Accepted:
May 08 2002
Citation
Adam Patkowski, Marian Paluch, Hartmut Kriegs; Dynamic light scattering studies of supercooled phenylphthalein–dimethylether dynamics under high pressure. J. Chem. Phys. 1 August 2002; 117 (5): 2192–2198. https://doi.org/10.1063/1.1489902
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