Crystallization kinetics of polyethylenes: A perspective from polymerization catalyst

Muhammad Atiqullah*, Atif Fazal, Abdurrahman Al-Harbi, Ikram Hussain, Anwar Hossaen

*Corresponding author for this work

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

Abstract

The isothermal crystallization of three ethylene homopolymers made using a laboratory-scale reactor under comparable polymerization conditions was studied to minimize the effects of varying hydrodynamics on polymer morphology. The surface chemistry and solid-state electronic environment of the catalysts significantly affected M, PDI, and linearity of the synthesized polymers. The residual catalyst could provide temperature-resistant heterogeneous nuclei, and interact on a molecular level to affect primary crystallization can be determined by calculating the concerned activation energy, bulk crystallization rate,a nd the Avrami rate constant. The surface chemistry and solid-state electronic environment of the residual catalysts influenced the dependence of Avrami rate constant on crystallization temperature, bulk crystallization rate, and % crystallinity, especially for the Z-N HomoPE. This is an abstract of a paper presented at the 20th Annual Saudi-Japan Symposium on Catalysts in Petroleum Refining and Petrochemicals (Dharan, Saudi Arabia 12/5-6/2010).

Original languageEnglish
Title of host publicationKing Fahd University of Petroleum and Minerals, Research Institute - 20th Annual Saudi-Japan Symposium on Catalysts in Petroleum Refining and Petrochemicals 2010
Pages151-153
Number of pages3
StatePublished - 2010

Publication series

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

ASJC Scopus subject areas

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

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