Preparation of functional ethoxysilane-containing polyethylene through ethylene coordination copolymerization catalyzed by iminopyrrolide vanadium complex
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Preparation of functional ethoxysilane-containing polyethylene through ethylene coordination copolymerization catalyzed by iminopyrrolide vanadium complex
LIU Zhiying, FAN Hong. Preparation of functional ethoxysilane-containing polyethylene through ethylene coordination copolymerization catalyzed by iminopyrrolide vanadium complex[J]. CIESC Journal, 2017, (2): 774-780.
DOI:
LIU Zhiying, FAN Hong. Preparation of functional ethoxysilane-containing polyethylene through ethylene coordination copolymerization catalyzed by iminopyrrolide vanadium complex[J]. CIESC Journal, 2017, (2): 774-780.DOI: 10.11949/j.issn.0438-1157.20160906.
Preparation of functional ethoxysilane-containing polyethylene through ethylene coordination copolymerization catalyzed by iminopyrrolide vanadium complex
was synthesized through hydrosilylation reaction of dimethylethoxysilane with 1
7-octadiene. Catalyzed by a vanadium complex bearing iminopyrrolide ligands (VCIP)
the functional ethoxysilane-containing polyethylenes (PE-co-OEMS) were synthesized by copolymerization of ethylene with OEMS. The structure and properties of PE-co-OEMSs were characterized with 1H NMR
13C NMR
HT-GPC and DSC. It was found that catalytic activity still remained 1.2 kg·mmol-1·h-1 when OEMS feeding reached to 60 mmol·L-1
and the OEMS incorporating in the copolymer was 1.3%(mol). Besides
the OEMS feeding had a great influence on the average molecular weight (Mw) and distribution (PDI) of copolymers. The Mw and PDI of PE-co-OEMS were 16900 and 2.1 when OEMS feeding was 30 mmol·L-1. With further increasing the OEMS feeding
Mw increased and PDI became wider. The melting temperature (Tm) and crystallization enthalpy (ΔHc) decreased with the increase of OEMS incorporation. The ethoxysilane-containing copolymers were easily crosslinked under the catalysis of trifluoromethanesulfonic acid
and the copolymer gel contents after crosslinking were nearly 100%.
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Related Author
JIN Zhen
FAN Hong
FEI Zhenghao
YANG Xiuzhi
LIU Zongtang
SHA Xinlong
LIU Runzhu
CHU Tiantian
Related Institution
State Key Laboratory of Chemical Engineering, College of Chemical and Biological Engineering, Zhejiang University
School of Chemistry and Environmental Engineering, Yancheng Teachers University
School of Chemistry and Chemical Engineering, Nanjing University
Key Laboratory of Carbon Fiber and Functional Polymers of Ministry of Education, College of Materials Science and Engineering, Beijing University of Chemical Technology
Tianjin Key Laboratory of Applied Catalysis Science and Technology, School of Chemical Engineering and Technology, Tianjin University