FOLLOWUS
a.School of Pharmaceutical Sciences, Changchun University of Chinese Medicine, Changchun 130117, China
b.Chemistry and Chemical Engineering Guangdong Laboratory, Shantou 515031, China
c.Key Laboratory of Engineering Plastics and Beijing National Laboratory for Molecular Science, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China
qaiser@ccelab.com.cn (Q.M.)
yuzx01@ccucm.edu.cn (Z.X.Y.)
whsun@iccas.ac.cn (W.H.S.)
Published:1 May 2024,
Published Online:26 December 2023,
Received:4 November 2023,
Revised:21 November 2023,
Accepted:27 November 2023
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Qin, L. D.; Wang, X. Y.; Mahmood, Q.; Yu, Z. X.; Wang, Y. Z.; Zou, S.; Liang, T. L.; Sun, W. H. High-performance α-diimine nickel complexes for facile access of PE elastomers with exceptional material properties. Chinese J. Polym. Sci. 2024, 42, 620–635
Li-Dong Qin, Xin-Yu Wang, Qaiser Mahmood, et al. High-Performance
Qin, L. D.; Wang, X. Y.; Mahmood, Q.; Yu, Z. X.; Wang, Y. Z.; Zou, S.; Liang, T. L.; Sun, W. H. High-performance α-diimine nickel complexes for facile access of PE elastomers with exceptional material properties. Chinese J. Polym. Sci. 2024, 42, 620–635 DOI: 10.1007/s10118-024-3073-0.
Li-Dong Qin, Xin-Yu Wang, Qaiser Mahmood, et al. High-Performance
In this study
symmetrical α-diimine nickel precatalysts displayed high activity (typically 10
6
- 10
7
g mol-1 h
−1
) and robust thermal stability for synthesizing highly branched polyethylene. Mechanical analysis demonstrated excellent tensile strength and strain recovery
highlighting the superior material properties of the prepared thermoplastic polyethylene elastomers.
For practicable elastomeric polyethylene
achieving high catalyst thermal stability and activity
along with precise control of polymer properties such as branching density
molecular weights
and distribution
is crucial but challenging. In this study
two sets of symmetrical
α
-diimine nickel complexes
each comprising four nickel bromide or chloride complexes
were synthesized and investigated their performance for ethylene polymerization under various reaction conditions. Upon activation with either Et
2
AlCl or MMAO cocatalysts
these complexes displayed not only high activity but also generated high molecular weight polyethylenes with controlled polydispersity and a substantial number of branches. The catalyst with the least steric hindrance displayed the remarkable high activity (up to 1.2×10
7
g·mol
−1
·h
−1
). Notably
nickel bromides demonstrated higher activity compared to their chloride counterparts. The investigation into the effect of reaction temperature on catalytic performance revealed that
NiBr
Me
-MMAO system displayed high thermal stability (activity up to 2.51×10
6
g·mol
−1
·h
−1
at 100 °C) and consistently yielded high polymer molecular weights with narrow polydispersity over a broad temperature range of 30−100 °C. Of significant note
mechanical analysis of the resulting polyethylene demonstrated excellent ultimate tensile strength and high strain at break. Particularly
the polyethylene sample prepared at 100 °C exhibited ultimate tensile strength up to 10 MPa with 1863% maximum strain at break and a strain recovery of up to 54.9% after ten cycles at a fixed strain of 300%
indicating excellent material properties of prepared thermoplastic polyethylene elastomers (TPE).
Thermoplastic polyethylene elastomersα-Diimine nickel pre-catalystsEthylene polymerizationMechanical propertiesHighly branched polyethylene
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