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@ARTICLE{Arbe:10767,
author = {Arbe, A. and Genix, A.-C. and Arrese-Igor, S. and
Colmenero, J. and Richter, D.},
title = {{D}ynamics in poly(n-alkyl methacrylates): {A} neutron
scattering, calorimetric and dielectric study},
journal = {Macromolecules},
volume = {43},
number = {6},
issn = {0024-9297},
address = {Washington, DC},
publisher = {Soc.},
reportid = {PreJuSER-10767},
pages = {3107 - 3119},
year = {2010},
note = {We thank the Institut Laue-Langevin (ILL) in Grenoble
(France) for neutron scattering facilities and the ILL
scientists P. Fouqttet, M. Maccarini, B. Deme, and P. P.
Deen for experimental help at the ILL. We are also thankful
to Prof. A. Alegria for fruitful discussions. This research
project has been supported by the European Commission NOE
SoftComp, Contract NMP3-CT-2004-502235, the "Donostia
International Physics Center". A.A. and J.C. acknowledge
support from the projects MAT2007-63681, IT-436-07 (GV), and
the Spanish Ministerio de Educacion y Ciencia (Grant
CSD2006-53).},
abstract = {Combining neutron diffraction, neutron spin echo,
differential scanning calorimetry, and dielectric
spectroscopy, we have investigated the structure and
dynamics of poly(n-butyl methacrylate) (PBMA) and
poly(n-hexyl methacrylate) (PHMA). Signatures of the
occurrence of a glass transition associated with the
freezing of the intermolecular correlations within alkyl
nanodomains are present in the structural data. Exploiting
isotopic labeling, neutron scattering has revealed
collective dynamics at the main-chain and side-group levels
for both polymers and the self-motions of hydrogen atoms in
the side groups of PHMA, adding valuable microscopic
information to comprehensive relaxation maps and putting the
relaxation results into a perspective. Moreover, we find
exotic dynamical behavior for the side groups, characterized
by extremely stretched (nearly logarithmic-like) decays of
the correlation functions. For PHMA, a complete dynamical
decoupling of side-group dynamics from the main-chain
motions is found. The side groups of this polymer show an
extremely "strong" temperature dependence of the structural
relaxation time and much faster characteristic times for
self than collective motions. The analogies found between
the self-motions of the side-group H atoms in PHMA and the
gamma-relaxation process in semicrystalline polyethylene
(PE) strengthen the picture of confined PE-like dynamics
within alkyl nanodomains. We discuss possible origins for
the observed phenomenology.},
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:000275711300057},
doi = {10.1021/ma902833h},
url = {https://juser.fz-juelich.de/record/10767},
}