Ethylene Polymerization over Metal-Organic Framework-Supported Zirconocene Complexes

YQ Wu, JM Dorresteijn, BM Weckhuysen*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Metallocene immobilization onto a solid support helps to overcome the drawbacks of homogeneous metallocene complexes in the catalytic olefin polymerization. In this study, valuable insights have been obtained into the effects of pore size, linker composition, and surface groups of metal–organic frameworks (MOFs) on their role as support materials for metallocene-based ethylene polymerization catalysis. Three distinct Zn-based metal–organic frameworks (MOFs), namely, MOF-5, IRMOF-3, and ZIF-8, with different linkers have been activated with methylaluminoxane (MAO) and zirconocene complexes, followed by materials characterization and testing for ethylene polymerization. Characterization has been performed by multiple analytical tools, including X-ray diffraction (XRD), scanning electron microscopy (SEM), gel permeation chromatography (GPC), differential scanning calorimetry (DSC), and CO Fourier transform infrared (FT-IR) spectroscopy. It was found that the interactions between MOFs, MAO, and the zirconocene complex not only lead to both catalyst activation and deactivation but also result in the creation of multiple active sites. By alteration of the MOF support, it is possible to obtain polyethylene with different properties. Notably, ultrahigh molecular weight polyethylene (UHMWPE, MW = 5.34 × 106) was obtained using IRMOF-3 as support. This study reveals the potential of MOF materials as tunable porous supports for metallocene catalysts active in ethylene polymerization.
Original languageEnglish
Pages (from-to)9093-9103
Number of pages11
JournalACS Catalysis
Volume14
Issue number11
DOIs
Publication statusPublished - 29 May 2024

Bibliographical note

Publisher Copyright:
© 2024 The Authors. Published by American Chemical Society.

Funding

Y.W. acknowledges the financial support from the Dalian Institute of Chemical Physics (DICP), Chinese Academy of Sciences for the Talent Training Project of DICP. The authors would like to thank Dr. Laurens D.B. Mandemaker and Christia Jabbour (Utrecht University, UU) for their helpful discussions. The authors would like to thank Dr. Shuang Yang, Dr. Xinwei Ye, and Hui Wang (Utrecht University, UU) for their help in the experiments. The authors also thank Virginie Cirriez, Alexandre Welle, and Sylvie Ligot (TotalEnergies) for helpful discussions and the GPC measurements. B.M.W. is supported by the Netherlands Organization for Scientific Research (NWO) in the frame of a Gravitation Program, MCEC (Netherlands Center for Multiscale Catalytic Energy Conversion), and the Advanced Research Center (ARC) Chemical Buildings Blocks Consortium (CBBC), a public\u2013private research consortium in the Netherlands (arc-cbbc.nl).

Funders
Nederlandse Organisatie voor Wetenschappelijk Onderzoek
Chinese Academy of Sciences for the Talent Training Project of DICP
Chemical Buildings Blocks Consortium
Netherlands Center for Multiscale Catalytic Energy Conversion
Advanced Research Center
MCEC
Dalian Institute of Chemical Physics, Chinese Academy of Sciences

    Keywords

    • Catalyst characterization
    • Ethylene polymerization
    • FT-IR spectroscopy
    • Metal-organic frameworks
    • Supported metallocene

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