

FOLLOWUS
a.State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China
b.School of Applied Chemistry and Engineering, University of Science and Technology of China, Hefei 230026, China
c.BASF Polyurethane Specialties (China) Co. Ltd., Shanghai 200137, China
d.V. Lit. Consult, Gozewijnstraat 4, 6191 WV Beek, the Netherlands
v.lit.con@kpnmail.nl (V.L.)
men@ciac.ac.cn (Y.F.M)
Received:07 March 2023,
Revised:2023-3-23,
Accepted:12 April 2023,
Online First:18 May 2023,
Published:01 December 2023
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Wang, H. R.; Litvinov, V.; Yu, W.; Peh, K. W. E.; Yu, Q. L.; Men, Y. F. Temperature-induced evolution of micro-structure and chain dynamics in thermoplastic polyurethane with low hard segment content as studied by in situ synchrotron SAXS and time-domain NMR experiments. Chinese J. Polym. Sci. 2023, 41, 1902–1911
Hong-Ru Wang, Victor Litvinov, Wei Yu, et al. Temperature-induced Evolution of Micro-structure and Chain Dynamics in Thermoplastic Polyurethane with Low Hard Segment Content as Studied by
Wang, H. R.; Litvinov, V.; Yu, W.; Peh, K. W. E.; Yu, Q. L.; Men, Y. F. Temperature-induced evolution of micro-structure and chain dynamics in thermoplastic polyurethane with low hard segment content as studied by in situ synchrotron SAXS and time-domain NMR experiments. Chinese J. Polym. Sci. 2023, 41, 1902–1911 DOI: 10.1007/s10118-023-2988-1.
Hong-Ru Wang, Victor Litvinov, Wei Yu, et al. Temperature-induced Evolution of Micro-structure and Chain Dynamics in Thermoplastic Polyurethane with Low Hard Segment Content as Studied by
The effect of temperature on the evolution of physical structures and chain dynamics of TPU with low hard segment content is studied using DSC
SAXS and Time-domain NMR. The SSA thermal fractionation analysis shows a wide length distribution of MDI-BD hard blocks. Softening of glassy fraction of hard blocks and melting of nanocrystals take place successively during heating. Hard and soft blocks are mixed on the scale above nanometers in the melt.
The microstructural evolution of a thermoplastic polyurethane (TPU) with low hard segment content has been monitored utilizing
in situ
real-time synchrotron small angle X-ray scattering (SAXS) and time-domain nuclear magnetic resonance (NMR) measurements. The TPU is composed of 23 wt% of [4
4-methylenediphenyl diisocyanate (MDI)]-[1
4-butanediol (BD)]
chain segments
which form hard domains
as [polytetrahydrofuran (PTHF)] forming soft domains. The number and distribution of monomer units in hard blocks is determined by the successive self-nucleation and annealing thermal fractionation technique.
In situ
SAXS method reveals heating-induced increase in the spacing of hard and soft domains
while time-domain
1
H-NMR characterizes the changes in the phase composition and chain dynamics in these domains. A glassy fraction of short MDI-BD chain segments in hard domains passes through
T
g
above ambient temperature. At higher temperatures
MDI-BD nanocrystals start to melt. Sequence length distribution of MDI-BD chain segments causes a distribution in crystal sizes and wide melting temperature range. The melting is accompanied by the mixing of MDI-BD with PTHF segments in soft domains
and by increase in segmental mobility in these domains. Above 180 °C
the TPU melt is homogeneous on the scale above nanometers according to SAXS data.
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