Real-time Monitoring of Living Cationic Ring-opening Polymerization of THF and Direct Prediction of Equilibrium Molecular Weight of PolyTHF
PAPER|Updated:2021-06-21
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Real-time Monitoring of Living Cationic Ring-opening Polymerization of THF and Direct Prediction of Equilibrium Molecular Weight of PolyTHF
Real-time Monitoring of Living Cationic Ring-opening Polymerization of THF and Direct Prediction of Equilibrium Molecular Weight of PolyTHF
Chinese Journal of Polymer Science2015年33卷第1期 页码:23-35
Affiliations:
State Key Laboratory of Chemical Resource Engineering, Key Laboratory of Carbon Fiber and Functional Polymers (Ministry of Education), Beijing University of Chemical Technology, Beijing 100029, China
Author bio:
**Yi-xian Wu (吴一弦), E-mail: yxwu@163.com
Funds:
National Natural Science Foundation of China(51173008;51221002)
An-ru Guo, Fan Yang, Rui Yu, 等. Real-time Monitoring of Living Cationic Ring-opening Polymerization of THF and Direct Prediction of Equilibrium Molecular Weight of PolyTHF[J]. Chinese Journal of Polymer Science, 2015,33(1):23-35.
An-ru Guo, Fan Yang, Rui Yu, et al. Real-time Monitoring of Living Cationic Ring-opening Polymerization of THF and Direct Prediction of Equilibrium Molecular Weight of PolyTHF[J]. Chinese Journal of Polymer Science, 2015, 33(1): 23-35.
An-ru Guo, Fan Yang, Rui Yu, 等. Real-time Monitoring of Living Cationic Ring-opening Polymerization of THF and Direct Prediction of Equilibrium Molecular Weight of PolyTHF[J]. Chinese Journal of Polymer Science, 2015,33(1):23-35.DOI: 10.1007/s10118-015-1571-9.
An-ru Guo, Fan Yang, Rui Yu, et al. Real-time Monitoring of Living Cationic Ring-opening Polymerization of THF and Direct Prediction of Equilibrium Molecular Weight of PolyTHF[J]. Chinese Journal of Polymer Science, 2015, 33(1): 23-35.DOI: 10.1007/s10118-015-1571-9.
Real-time Monitoring of Living Cationic Ring-opening Polymerization of THF and Direct Prediction of Equilibrium Molecular Weight of PolyTHF
A convenient real-time monitoring of monomer concentration during living cationic ring-opening polymerizations of tetrahydrofuran (THF) initiated with methyl triflate (MeOTf) has been developed for kinetic investigation and determination of equilibrium monomer concentration ([M]
e
)
via in situ
FTIR spectroscopy in combination with a diamond tipped attenuated total reflectance (ATR) immersion probe. The polymerization rate was first order with respect to monomer concentration and initiator concentration from the linear slope of ln([M]
0
−[M]
e
)/([M]−[M]
e
) versus polymerization time at different temperatures in various solvents. [M]
e
decreased linearly with initial monomer concentration while increased exponentially with increasing polymerization temperature. The equilibrium also strongly depends on solvent polarity and its interaction with monomer. The equilibrium polymerization time (
t
e
) decreased with increasing solvent polarity and decreased linearly with increasing [M]
0
in three solvents with different slopes to the same point of bulk polymerization in the absence of solvent. Equation of
M
n
e
= 72.1/(0.14–0.04[M]
e
) has been established to provide a simple and effective approach for the prediction for the number-average molecular weight of polyTHFs at equilibrium state (
M
n
e
) in the equilibrium living cationic ring-opening polymerization of THF at 0 °C.
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