

FOLLOWUS
a.National Synchrotron Radiation Laboratory, Anhui Provincial Engineering Laboratory of Advanced Functional Polymer Film, CAS Key Laboratory of Soft Matter Chemistry, University of Science and Technology of China, Hefei 230026, China
b.Department of Accelerator Science and Engineering Physics, School of Nuclear Science and Technology, University of Science and Technology of China, Hefei 230026, China
c.Institute of Chemical Materials, China Academy of Engineering Physics, Mianyang 621900, China
lbli@ustc.edu.cn (L.B.L.)
wc003@ustc.edu.cn (W.C.)
Received:07 April 2024,
Revised:2024-05-06,
Accepted:14 May 2024,
Online First:20 August 2024,
Published:30 November 2024
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Xiong, Y. Q.; Li, C. L.; Lu, A.; Li, L. B.; Chen, W. Conformational disorder within the crystalline region of silica-filled polydimethylsiloxane: a solid-state NMR study. Chinese J. Polym. Sci. 2024, 42, 1780–1792
Yu-Qi Xiong, Chang-Lin Li, Ai Lu, et al. Conformational Disorder Within the Crystalline Region of Silica-Filled Polydimethylsiloxane: A Solid-State NMR Study[J]. Chinese Journal of Polymer Science, 2024, 42(11): 1780-1792.
Xiong, Y. Q.; Li, C. L.; Lu, A.; Li, L. B.; Chen, W. Conformational disorder within the crystalline region of silica-filled polydimethylsiloxane: a solid-state NMR study. Chinese J. Polym. Sci. 2024, 42, 1780–1792 DOI: 10.1007/s10118-024-3164-y.
Yu-Qi Xiong, Chang-Lin Li, Ai Lu, et al. Conformational Disorder Within the Crystalline Region of Silica-Filled Polydimethylsiloxane: A Solid-State NMR Study[J]. Chinese Journal of Polymer Science, 2024, 42(11): 1780-1792. DOI: 10.1007/s10118-024-3164-y.
Using solid-state NMR
synchrotron WAXS
and TMDSC techniques
silica filler-induced crystalline chain conformational disorder in silicone rubber composites was first discovered
elucidating the impact of fillers on crystalline chain conformational order.
The crystallization behavior of silica-filled polydimethylsiloxane (PDMS) was investigated in detail by
1
H solid-state nuclear magnetic resonance (
1
H SS-NMR) in combination with synchrotron radiation wide-angle X-ray scattering (WAXS)
and temperature-modulated differential scanning calorimetry (TMDSC) techniques. For neat PDMS
no apparent difference is observed for the crystallinity characterized by
1
H SS-NMR and WAXS at low-temperature regions. However
upon filler addition
a 15%−35% lower difference in crystallinity is observed measured by
1
H SS-NMR compared to WAXS. The origin of such mismatch was explored through multi-component structural
dynamics
and chain-order analysis of PDMS samples with different filler fractions. The 1D integrated WAXS results of PDMS with different filler fractions at different temperatures show that the packing structure as well as crystal size basically remain unchanged
but as the filler fraction increases from 0 phr to 60 phr
the rigid component’s dynamics order parameter
S
r
obtained by
1
H SS-NMR decreases from 0.70 to 0.55. The filler fraction-dependent crystallinity calculated based on
S
r
was compared with experimental values
revealing a behavior of decreasing order in the crystalline region. Combining with the results of accelerated chain dynamics in crystalline region as reflected by
T
2
values
the molecular origin is attributed to the formation of CONDIS crystals
whose conformational order is lost but the position and orientation orders are kept. Such hypothesis is further supported by the TMDSC results
where
as the filler fraction increases from 0 phr to 60 phr
the melting range widens from 8.77 K to 14.56 K
representing a growth of 166%. In addition to previous reports related to the condition for forming CONDIS mesophase
i.e.
temperature
pressure
and stretching
the nano-sized filler could also introduce the local conformational disorder for chain packing.
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