Abstract
AbstractA high‐activity Ziegler–Natta catalyst of TiCl4‐supported MgCl2 (ethoxide type) was prepared. Ethyl benzoate (EB) and polydimethylsiloxane (PDMS) were used as internal donors, while p‐methyl toluate (MPT) and triethylaluminum (TEA) were used as the external donor and cocatalyst, respectively. Suspension copolymerization of ethylene–propylene (EPM) was carried out in n‐heptane using the catalyst system. The relative pressures of 1.5 : 1 and 2 : 1 atmosphere of propylene‐to‐ethylene (PP/PE) gave a polymer with elastomeric properties. The relative pressure of propylene‐to‐ethylene higher and lower than the above values, however, gave a homopolymer or copolymer without elastomeric properties. The effect of the TEA concentration, H2 concentration, temperature, and pressure of PP/PE on the yield of the polymer obtained was investigated. The effects of these factors on the glass transition temperature (Tg) and ethylene content of the polymer were studied. The content of ethylene in EPM was determined using the FTIR technique. The molar ratio of Al : MPT : Ti = 355 : 107 : 1 gave a polymer with an ethylene content of about 32%. However, a ratio lower than AL : MPT : Ti = 355 : 107 : 1 did not give a good elastomeric polymer. The highest productivity of the catalyst was obtained at a molar ratio of AL : MPT : Ti = 355 : 107 : 1. Increasing the temperature from 45 to 70°C caused a slight increase of Et % content and a decrease of the Tg of the copolymer obtained, while the highest productivity of the catalyst was obtained at 55°C with good elastomeric properties using an AL : MPT : Ti = 497 : 107 : 1 molar ratio. Increasing the pressure of propylene from 1.5 to 2.5 atm caused a sharp decrease in the Tg and ethylene content of the polymer. When the ethylene content in the copolymer was increased, the Tg value had a tendency to be closer to the polyethylene Tg. © 2002 John Wiley & Sons, Inc. J Appl Polym Sci 84: 785–790, 2002; DOI 10.1002/app.10330
Published Version
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.