Segmental Dynamics in Poly(methylphenylsiloxane) Networks by Dielectric Relaxation Spectroscopy

1999 ◽  
Vol 32 (10) ◽  
pp. 3518-3527 ◽  
Author(s):  
Benjamin D. Fitz ◽  
Jovan Mijovic
RSC Advances ◽  
2017 ◽  
Vol 7 (65) ◽  
pp. 40745-40754 ◽  
Author(s):  
Oguzhan Oguz ◽  
Stefanos A. Koutsoumpis ◽  
Eren Simsek ◽  
Emel Yilgor ◽  
Iskender Yilgor ◽  
...  

The effect of poly(ethylene oxide) (PEO) soft segment molecular weight (Mn= 2000, 4600, 8000 g mol−1) molecular mobility and segmental dynamics of a series of polyurethane–urea copolymers (PU) was investigated by dielectric relaxation spectroscopy.


2017 ◽  
Vol 19 (2) ◽  
pp. 1389-1394 ◽  
Author(s):  
Toyoaki Hirata ◽  
Hisao Matsuno ◽  
Daisuke Kawaguchi ◽  
Manabu Inutsuka ◽  
Tomoyasu Hirai ◽  
...  

The segmental dynamics of poly(2-methoxyethyl acrylate) at the water interface is extremely faster and comparable to the side chain motion.


1998 ◽  
Vol 543 ◽  
Author(s):  
S. H. Anastasiadis ◽  
K. Karatasos ◽  
G. Vlachos ◽  
E. Manias ◽  
E. P. Giannelis

AbstractThe local segmental dynamics of polymers confined within the 15–20 Å interlayer spacing of nanocomposites consisting of poly(methyl phenyl siloxane) intercalated within organically modified silicates, has been investigated utilizing Dielectric Relaxation Spectroscopy. The effect of confinement on the local reorientational dynamics is evident by the observation of a relaxation mode, which is much faster than the segmental α-relaxation of the bulk polymer and exhibits much weaker temperature dependence. This is attributed to the restrictions placed by the interlayer spacing on the cooperative volume required for the ax-relaxation.


1990 ◽  
Vol 45 (2) ◽  
pp. 126-134
Author(s):  
E. Dachwitz

AbstractThe permittivity of the title solutions has been measured at frequencies between some MHz and 72 GHz at 20 °C. Polyvinyl pyrrolidone of relative molar mass ranging from 1200 to 360 000 has been used. Referring to the concentration of monomeric repeat units (x = 0.65 maximum) there is no significant chain length effect. The permittivity data are described in terms of discrete Debye type spectral components. Special attention is paid to the contributions ascribable to the solvents, which are discussed with respect to their solvation behaviour. This can be described by a three state solvent model as follows. Besides the "bulk" solvent a further contribution is found in any case which is due to loosely affected (slowed down) solvent. Moreover a part of the solvent appears to be tightly bound to the polymer at high concentrations. All the solvents considered show similar solvation properties, notwithstanding their different tendencies towards selfassociation.


2007 ◽  
Vol 60 (1) ◽  
pp. 6 ◽  
Author(s):  
Simon Schrödle ◽  
Gary Annat ◽  
Douglas R. MacFarlane ◽  
Maria Forsyth ◽  
Richard Buchner ◽  
...  

A study of the room-temperature ionic liquid N-methyl-N-ethylpyrrolidinium dicyanamide by dielectric relaxation spectroscopy over the frequency range 0.2 GHz ≤ ν ≤ 89 GHz has revealed that, in addition to the already known lower frequency processes, there is a broad featureless dielectric loss at higher frequencies. The latter is probably due to the translational (oscillatory) motions of the dipolar ions of the IL relative to each other, with additional contributions from their fast rotation.


2008 ◽  
Vol 265 (1) ◽  
pp. 12-20 ◽  
Author(s):  
Polycarpos Pissis ◽  
Daniel Fragiadakis ◽  
Athanasios Kanapitsas ◽  
Kostas Delides

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