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@ARTICLE{Goracci:281716,
author = {Goracci, Guido and Arbe, Arantxa and Alegría, Angel and
García Sakai, Victoria and Rudić, Svemir and Schneider,
Gerald J. and Lohstroh, Wiebke and Juranyi, Fanni and
Colmenero, Juan},
title = {{I}nfluence of {S}olvent on
{P}oly(2-({D}imethylamino){E}thyl {M}ethacrylate) {D}ynamics
in {P}olymer-{C}oncentrated {M}ixtures: {A} {C}ombined
{N}eutron {S}cattering, {D}ielectric {S}pectroscopy, and
{C}alorimetric {S}tudy},
journal = {Macromolecules},
volume = {48},
number = {18},
issn = {1520-5835},
address = {Washington, DC},
publisher = {Soc.},
reportid = {FZJ-2016-01404},
pages = {6724 - 6735},
year = {2015},
note = {"final draft post referee" kann nicht beigebracht werden},
abstract = {We have investigated the dynamical
processes—α-relaxation, local motions of the side-groups,
and methyl group rotations—in poly(2-(dimethylamino)ethyl
methacrylate) (PDMAEMA) in the dry state and in mixtures (at
70 $wt\%$ polymer concentration) with tetrahydrofuran (THF)
and water, to address the question as to how these polymer
motions are affected by plasticizers interacting in
different ways with the polymer. Differential scanning
calorimetry, dielectric spectroscopy, and neutron scattering
techniques on labeled samples (with deuterated solvents to
isolate the signal of the polymer component) have been
combined. The α-relaxation is drastically affected, with
similar shifts of the glass-transition temperature for both
solvents. Effects of compositional heterogeneities and
reduction of the fragility are also observed. On the
contrary, methyl-group dynamics are unaffected by the
presence of solvent. Regarding side-group local motions
(β-relaxation), two kinds of components—a slow and a fast
one—could be identified in the dry state. On the basis of
the spatial information provided by neutron scattering, a
model for the geometry of the motions involved in the fast
component has been proposed. Adding solvent, this process
would remain essentially unaltered, but the population
involved in the slower one would be reduced. With THF as
solvent, this reduction would be complete, but with water it
would be only partial. This could be attributed to rather
heterogeneous distribution of water molecules in the polymer
likely associated with the presence of water clusters. Such
a scenario would also explain the much more pronounced
broadening of the glass-transition region observed for the
polymer in the aqueous mixture with respect to that induced
by THF.},
cin = {JCNS (München) ; Jülich Centre for Neutron Science JCNS
(München) ; JCNS-FRM-II / Neutronenstreuung ; JCNS-1},
ddc = {540},
cid = {I:(DE-Juel1)JCNS-FRM-II-20110218 /
I:(DE-Juel1)JCNS-1-20110106},
pnm = {6G15 - FRM II / MLZ (POF3-6G15) / 6G4 - Jülich Centre for
Neutron Research (JCNS) (POF3-623)},
pid = {G:(DE-HGF)POF3-6G15 / G:(DE-HGF)POF3-6G4},
experiment = {EXP:(DE-MLZ)SPHERES-20140101 /
EXP:(DE-MLZ)TOF-TOF-20140101},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000361935600040},
doi = {10.1021/acs.macromol.5b01316},
url = {https://juser.fz-juelich.de/record/281716},
}