Ethylene insertion in the presence of new alkoxysilane electron donors for Ziegler-Natta catalyzed polyethylene

© 2017 Density functional theory (DFT) calculations have been carried out to investigate the ethylene insertion pathway using a Ziegler-Natta catalyst in the absence and presence of electron donor (ED) systems on the (1 1 0) MgCl 2 surface. The coadsorptions of four different EDs i.e. Si(OEt) m Cl n...

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Main Authors: Sutiam Kruawan, Manussada Ratanasak, Rungroj Chanajaree, Thanyada Rungrotmongkol, Oraphan Saengsawang, Vudhichai Parasuk, Nawee Kungwan, Supot Hannongbua
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Published: 2018
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http://cmuir.cmu.ac.th/jspui/handle/6653943832/46368
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spelling th-cmuir.6653943832-463682018-04-25T07:22:32Z Ethylene insertion in the presence of new alkoxysilane electron donors for Ziegler-Natta catalyzed polyethylene Sutiam Kruawan Manussada Ratanasak Rungroj Chanajaree Thanyada Rungrotmongkol Oraphan Saengsawang Vudhichai Parasuk Nawee Kungwan Supot Hannongbua Chemistry Agricultural and Biological Sciences © 2017 Density functional theory (DFT) calculations have been carried out to investigate the ethylene insertion pathway using a Ziegler-Natta catalyst in the absence and presence of electron donor (ED) systems on the (1 1 0) MgCl 2 surface. The coadsorptions of four different EDs i.e. Si(OEt) m Cl n (m + n = 4) were investigated. The presence of Si(OEt) 4 on the (1 1 0) MgCl 2 surface with the preferential bidentate mode was found to have the strongest adsorption energy (ΔE ads ). The potential energy surface (PES) map indicated that the reaction mechanism of the ethylene insertion into the Ti[sbnd]C bond on the (1 1 0) Mg 13 Cl 26 .TiCl 3 -CH 2 CH 3 surface is pseudo-concerted. As the differences in the intrinsic activation energies (ΔE a ) obtained from all systems are so small, this energy cannot be used to fully explain the significant changes in the rates of the ethylene insertion reaction observed when an ED is employed. Here, the apparent activation energy (ΔΔE aa ) was calculated using the PBE functional and the 6-31G(d, p) basis set for C, H, O, Mg and Cl, and the LANL2DZ basis set with an ECP function for the Ti atom. All EDs presented in this work in the ethylene insertion reaction can significantly reduce the apparent energy barrier when compared to an absence of any ED system. The obtained ΔΔE aa for the four ED complexes were found to decrease in the following order: SiOEtCl 3   >  Si(OEt) 2 Cl 2   >  Si(OEt) 3 Cl  >  Si(OEt) 4 . The obtained data lead to the conclusion that Si(OEt) 4 is the most suitable ED to increase the productivity of PE in the presence of alkoxysilane. 2018-04-25T06:53:52Z 2018-04-25T06:53:52Z 2017-07-15 Journal 2210271X 2-s2.0-85018624812 10.1016/j.comptc.2017.04.002 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85018624812&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/46368
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Chemistry
Agricultural and Biological Sciences
spellingShingle Chemistry
Agricultural and Biological Sciences
Sutiam Kruawan
Manussada Ratanasak
Rungroj Chanajaree
Thanyada Rungrotmongkol
Oraphan Saengsawang
Vudhichai Parasuk
Nawee Kungwan
Supot Hannongbua
Ethylene insertion in the presence of new alkoxysilane electron donors for Ziegler-Natta catalyzed polyethylene
description © 2017 Density functional theory (DFT) calculations have been carried out to investigate the ethylene insertion pathway using a Ziegler-Natta catalyst in the absence and presence of electron donor (ED) systems on the (1 1 0) MgCl 2 surface. The coadsorptions of four different EDs i.e. Si(OEt) m Cl n (m + n = 4) were investigated. The presence of Si(OEt) 4 on the (1 1 0) MgCl 2 surface with the preferential bidentate mode was found to have the strongest adsorption energy (ΔE ads ). The potential energy surface (PES) map indicated that the reaction mechanism of the ethylene insertion into the Ti[sbnd]C bond on the (1 1 0) Mg 13 Cl 26 .TiCl 3 -CH 2 CH 3 surface is pseudo-concerted. As the differences in the intrinsic activation energies (ΔE a ) obtained from all systems are so small, this energy cannot be used to fully explain the significant changes in the rates of the ethylene insertion reaction observed when an ED is employed. Here, the apparent activation energy (ΔΔE aa ) was calculated using the PBE functional and the 6-31G(d, p) basis set for C, H, O, Mg and Cl, and the LANL2DZ basis set with an ECP function for the Ti atom. All EDs presented in this work in the ethylene insertion reaction can significantly reduce the apparent energy barrier when compared to an absence of any ED system. The obtained ΔΔE aa for the four ED complexes were found to decrease in the following order: SiOEtCl 3   >  Si(OEt) 2 Cl 2   >  Si(OEt) 3 Cl  >  Si(OEt) 4 . The obtained data lead to the conclusion that Si(OEt) 4 is the most suitable ED to increase the productivity of PE in the presence of alkoxysilane.
format Journal
author Sutiam Kruawan
Manussada Ratanasak
Rungroj Chanajaree
Thanyada Rungrotmongkol
Oraphan Saengsawang
Vudhichai Parasuk
Nawee Kungwan
Supot Hannongbua
author_facet Sutiam Kruawan
Manussada Ratanasak
Rungroj Chanajaree
Thanyada Rungrotmongkol
Oraphan Saengsawang
Vudhichai Parasuk
Nawee Kungwan
Supot Hannongbua
author_sort Sutiam Kruawan
title Ethylene insertion in the presence of new alkoxysilane electron donors for Ziegler-Natta catalyzed polyethylene
title_short Ethylene insertion in the presence of new alkoxysilane electron donors for Ziegler-Natta catalyzed polyethylene
title_full Ethylene insertion in the presence of new alkoxysilane electron donors for Ziegler-Natta catalyzed polyethylene
title_fullStr Ethylene insertion in the presence of new alkoxysilane electron donors for Ziegler-Natta catalyzed polyethylene
title_full_unstemmed Ethylene insertion in the presence of new alkoxysilane electron donors for Ziegler-Natta catalyzed polyethylene
title_sort ethylene insertion in the presence of new alkoxysilane electron donors for ziegler-natta catalyzed polyethylene
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85018624812&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/46368
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