Real-time Monitoring of Living Cationic Ring-opening Polymerization of THF and Direct Prediction of Equilibrium Molecular Weight of PolyTHF

Citation: An-ru Guo, Fan Yang, Rui Yu, Yi-xian Wu. 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 shu

Real-time Monitoring of Living Cationic Ring-opening Polymerization of THF and Direct Prediction of Equilibrium Molecular Weight of PolyTHF

An-ru Guo ^1, ,
Fan Yang ^1, ,
Rui Yu ^1, ,
Yi-xian Wu ^{1,
,}

1.
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

通讯作者: Yi-xian Wu,

基金项目:
This work was financially supported by the National Natural Science Foundation of China (Nos. 51173008 and 51221002).

摘要: 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 (te) 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 Mn,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 (Mn,e) in the equilibrium living cationic ring-opening polymerization of THF at 0 ℃.

关键词:

English

Real-time Monitoring of Living Cationic Ring-opening Polymerization of THF and Direct Prediction of Equilibrium Molecular Weight of PolyTHF

An-ru Guo ^1, ,
Fan Yang ^1, ,
Rui Yu ^1, ,
Yi-xian Wu ^{1,
,}

1.
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

Corresponding author: Yi-xian Wu,

Received Date: 05 March 2014
Revised Date: 03 April 2014
Available Online: 05 January 2015
Fund Project:
This work was financially supported by the National Natural Science Foundation of China (Nos. 51173008 and 51221002).

Abstract: 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 (te) 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 Mn,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 (Mn,e) in the equilibrium living cationic ring-opening polymerization of THF at 0 ℃.

Key words:

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1.
沈阳化工大学材料科学与工程学院沈阳 110142

Real-time Monitoring of Living Cationic Ring-opening Polymerization of THF and Direct Prediction of Equilibrium Molecular Weight of PolyTHF

通讯作者: Yi-xian Wu,

English

Real-time Monitoring of Living Cationic Ring-opening Polymerization of THF and Direct Prediction of Equilibrium Molecular Weight of PolyTHF

Corresponding author: Yi-xian Wu,

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通讯作者: 陈斌, bchen63@163.com

中国化学会秘书处

Real-time Monitoring of Living Cationic Ring-opening Polymerization of THF and Direct Prediction of Equilibrium Molecular Weight of PolyTHF

通讯作者: Yi-xian Wu,

English

Real-time Monitoring of Living Cationic Ring-opening Polymerization of THF and Direct Prediction of Equilibrium Molecular Weight of PolyTHF

Corresponding author: Yi-xian Wu,

CCS Chemistry：嵌段共聚物自组装成 “三明治”二维有机材料，实现纳米级压力传感功能

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