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@ARTICLE{Gerstl:10520,
author = {Gerstl, C. and Schneider, G. J. and Pyckhout-Hintzen, W.
and Allgaier, J. and Richter, D. and Alegria, A. and
Colmenero, J.},
title = {{S}egmental and normal mode relaxation of poly(alkylene
oxide)s studied by dielectric spectroscopy and rheology},
journal = {Macromolecules},
volume = {43},
issn = {0024-9297},
address = {Washington, DC},
publisher = {Soc.},
reportid = {PreJuSER-10520},
pages = {4968 - 4977},
year = {2010},
note = {The present work has been carried out in the frame of the
Joint Programme of Activities of the SoftComp Network of
Excellence (Contract NMP3-VT-2004-502235) granted under the
FP6 by the European Commission. C.G. acknowledges financial
support by the International Helmholtz Research School of
Biophysics and Soft Matter (IHRS BioSoft). A.A. and J.C.
acknowledge the financial support provided by the Donostia
International Physics Center (DIPC), the Basque Country
Government (Ref. IT-436-07, Depto. Educacion, Universidades
e Investigacion), and the Spanish Ministry of Science and
Innovation (Grant MAT 2007-63681).},
abstract = {A series of poly(alkylene oxide)s (PAO's) with different
lengths of the side chains and two different molecular
weights were studied by means of differential scanning
calorimetry, dielectric spectroscopy (BDS), and rheology.
The glass transition temperatures are almost independent of
molar mass and the length of the side chains, which is also
reflected by the dielectric a-relaxation, which depends only
slightly on the different samples. However, the
corresponding maxima in the dielectric loss of the samples
with longer side chains show a shoulder at high frequencies
with a temperature-dependent shape. The shape of the normal
mode changes slightly with the molar mass and the length of
the side chain. The normal mode relaxation times show a
molar-mass-dependent behavior indicating a significant
increase of the entanglement molecular weight M-e with
increasing length of the side group. A Rouse mode analysis
incorporating the molar mass distribution was performed but
could not reproduce the experimental data of the normal mode
process completely. The relaxation times obtained by
rheology agree well with the dielectric results, and
estimates of M-e based on the number of entanglements and on
the packing model confirm the values suggested by BDS. A
comparison of the estimated chain dimensions with literature
data supports the reliability of our calculations.},
keywords = {J (WoSType)},
cin = {IFF-5 / IFF-4 / Jülich Centre for Neutron Science JCNS
(JCNS) ; JCNS},
ddc = {540},
cid = {I:(DE-Juel1)VDB785 / I:(DE-Juel1)VDB784 /
I:(DE-Juel1)JCNS-20121112},
pnm = {BioSoft: Makromolekulare Systeme und biologische
Informationsverarbeitung / Großgeräte für die Forschung
mit Photonen, Neutronen und Ionen (PNI)},
pid = {G:(DE-Juel1)FUEK505 / G:(DE-Juel1)FUEK415},
shelfmark = {Polymer Science},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000278109700018},
doi = {10.1021/ma100384j},
url = {https://juser.fz-juelich.de/record/10520},
}