Abstract
Polypropylene (PP) prepared with the MgCl2/TiCl4–AlEt3/Ph2Si(OMe)2 catalyst system was fractionated by a preparative temperature rising elution fractionation (TREF) technique in the wide temperature range of room temperature to 130°C. The results of fractionation showed that there were plural active sites in this heterogeneous catalyst. Some key fractions were selected for characterization of 1H- and 13C-NMR. 1H-NMR results suggested that the fractionation takes place according to tacticity. Based on analysis of 13C-NMR, it was concluded that the polymerization mechanism proceeding on highly stereospecific active sites was active site-controlled and nonstereospecific active sites were able to convert into syndiotactic active sites during the polymerization, which led to the formation of a syn-diotactic block. © 1996 John Wiley & Sons, Inc.
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.