Copolymerization of ethylene and isoprene initiated by metallocene catalyst

In this study, we explore the dynamic nature of metallocene catalysts during ethylene/isoprene E/IP) copolymerization, with a focus on the influence of various reaction parameters. Challenges, why do olefinic catalysts show lower activity and molecular weight (Mw) at higher temperatures and low activity with higher diene content? Firstly, we investigate the observed phenomena of decreased catalyst activity and Mw at elevated temperatures using 1.25 μmole of the metallocene. Notably, a substantial increase in active sites from 30 °C to 40 °C, reaching a peak of 89 %. Surprisingly, further temperature increments lead to a noticeable decline in active sites. At 30 °C, the active site primarily engages in the insertion of IP through 3,4 connections, with no detectable cis-1,4 or trans-1,4 connections, which suggests a lack of stereoselectivity at this temperature. At 40–50°C, cis/trans-1,4 connections and active sites are approaching a higher level. This implies a reduction in chain transfer reactions, making catalytic active sites more favorable to cis/trans-1,4 connections. Secondly, we observe a remarkable impact of IP concentration in the E/IP copolymers, active centers, and activity show stability when the amount of IP was 0.116–0.48 mol/L and then started to decline when the amount of IP 0.96 mol/L, indicating a threshold beyond which deactivation occurs. Increasing IP concentration not only reduces activity and active sites but also fails to reactivate dormant polyethylene sites. The Mw and active centers of copolymers progressively decrease with elevated IP concentration, suggesting a faster chain transfer reaction with IP compared to E.

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Publication Details

Journal
Arabian Journal of Chemistry
Published
2024-09-12
DOI
https://doi.org/10.1016/j.arabjc.2024.105989
Citations
7
Primary Topic
Organometallic Complex Synthesis and Catalysis
Type
article
Field-Weighted Citation Impact
1.75

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article

Copolymerization of ethylene and isoprene initiated by metallocene catalyst

Jamile Mohammadi Moradian, Muhammad Nadeem, Shahid Ali Khan, Naushad Ahmad et al.
7 citations
Arabian Journal of Chemistry
Organometallic Complex Synthesis and Catalysis
1.75
article

Copolymerization of ethylene and isoprene initiated by metallocene catalyst

Jamile Mohammadi Moradian, Muhammad Nadeem, Shahid Ali Khan, Naushad Ahmad, Adnan Murad Bhayo, Li Guo, Rai Nauman Ali, Amjad Ali, Zhiqiang Fan, Jianwei Lu, Syed Najeeb-Uz-Zaman Haider, Ahmad Naveed
article en
7 citations

Abstract

In this study, we explore the dynamic nature of metallocene catalysts during ethylene/isoprene E/IP) copolymerization, with a focus on the influence of various reaction parameters. Challenges, why do olefinic catalysts show lower activity and molecular weight (Mw) at higher temperatures and low activity with higher diene content? Firstly, we investigate the observed phenomena of decreased catalyst activity and Mw at elevated temperatures using 1.25 μmole of the metallocene. Notably, a substantial increase in active sites from 30 °C to 40 °C, reaching a peak of 89 %. Surprisingly, further temperature increments lead to a noticeable decline in active sites. At 30 °C, the active site primarily engages in the insertion of IP through 3,4 connections, with no detectable cis-1,4 or trans-1,4 connections, which suggests a lack of stereoselectivity at this temperature. At 40–50°C, cis/trans-1,4 connections and active sites are approaching a higher level. This implies a reduction in chain transfer reactions, making catalytic active sites more favorable to cis/trans-1,4 connections. Secondly, we observe a remarkable impact of IP concentration in the E/IP copolymers, active centers, and activity show stability when the amount of IP was 0.116–0.48 mol/L and then started to decline when the amount of IP 0.96 mol/L, indicating a threshold beyond which deactivation occurs. Increasing IP concentration not only reduces activity and active sites but also fails to reactivate dormant polyethylene sites. The Mw and active centers of copolymers progressively decrease with elevated IP concentration, suggesting a faster chain transfer reaction with IP compared to E.

Arabian Journal of ChemistryVol. 17(11)
Jiangsu University (CN), King Saud University (SA), Wuchang University of Technology (CN), Zhejiang University (CN), University of Silesia in Katowice (PL), McMaster University (CA)
King Saud University
Openalex Percentile: Top 16%
Organometallic Complex Synthesis and Catalysis
1.75
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