Methylaluminoxane-activated polyolefin precatalysts: An applied research approach

Muhammad Atiqullah*

*Corresponding author for this work

Research output: Chapter in Book/Report/Conference proceedingConference contributionpeer-review

Abstract

The effects of hydrodynamic boundary layer mass transfer, methylaluminoxane anion design, and comonomer steric hindrance - on non-Z-N-catalyzed ethylene polymerization were studied. These variables significantly influenced catalyst productivity and copolymer microstructure, which eventually influenced the resulting polyethylene thermal behavior (melting and crystallization). The comonomer-induced structural/enchainment defects and the eventual partial disruption of the crystal package of the polyethylene chains were successfully modeled using Flory and Gibbs-Thompson equations. The models, combined with experiments, generated insightful new results. This is an abstract of a paper presented at the 25th Annual Saudi-Japan Symposium on Catalysts in Petroleum Refining and Petrochemicals 2015 (Dhahran, Saudi Arabia 12/7-8/2015).

Original languageEnglish
Title of host publicationKing Fahd University of Petroleum and Minerals, Research Institute - 25th Annual Saudi-Japan Symposium on Catalysts in Petroleum Refining and Petrochemicals 2015
PublisherKing Fahd University of Petroleum and Minerals
Pages117-129
Number of pages13
ISBN (Electronic)9781510820098
StatePublished - 2015

Publication series

NameKing Fahd University of Petroleum and Minerals, Research Institute - Annual Catalysts in Petroleum Refining and Petrochemicals Symposium Papers
Volume2015-January

Keywords

  • Boundary layer mass transfer
  • Intra-chain backbone inhomogeneity
  • Lamellar thickness distribution
  • MAO-activated precatalysts
  • Pseudo-homogeneous and in-situ ethylene-α-olefin copolymerization
  • Thermal properties

ASJC Scopus subject areas

  • Catalysis
  • General Chemistry
  • Fuel Technology
  • Energy Engineering and Power Technology

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