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Propylene polymerization with catalysts containing divalent titanium

Albizzati, E. ; Giannini, U. ; Balbontin, G. ; Camurati, I. ; Chadwick, J. C. ; Dall'occo, T. ; Dubitsky, Y. ; Galimberti, M. ; Morini, G. ; Maldotti, A.

Journal of polymer science. Part A, Polymer chemistry, 1997-09, Vol.35 (13), p.2645-2652

New York: John Wiley & Sons, Inc

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  • Título:
    Propylene polymerization with catalysts containing divalent titanium
  • Autor: Albizzati, E. ; Giannini, U. ; Balbontin, G. ; Camurati, I. ; Chadwick, J. C. ; Dall'occo, T. ; Dubitsky, Y. ; Galimberti, M. ; Morini, G. ; Maldotti, A.
  • Assuntos: Applied sciences ; catalyst decay ; Exact sciences and technology ; hydrogen activation ; Organic polymers ; Physicochemistry of polymers ; Polymerization ; Preparation, kinetics, thermodynamics, mechanism and catalysts ; propylene polymerization ; titanium oxidation state
  • É parte de: Journal of polymer science. Part A, Polymer chemistry, 1997-09, Vol.35 (13), p.2645-2652
  • Notas: istex:EB25FB8882B58BD64B6325D76F5C98656F5D2B88
    ark:/67375/WNG-D6LZCL3G-G
    ArticleID:POLA11
  • Descrição: The behavior in propylene polymerization of divalent titanium compounds of type [η6‐areneTiAl2Cl8], both as such and supported on activated MgCl2, has been studied and compared to that of the simple catalyst MgCl2/TiCl4. Triethylaluminium was used as cocatalyst. The Ti–arene complexes were active both in the presence and in the absence of hydrogen, in contrast to earlier reports that divalent titanium species are active for ethylene but not for propylene polymerization. 13C‐NMR analysis of low molecular weight polymer fractions indicated that the hydrogen activation effect observed for the MgCl2‐supported catalysts should be ascribed to reactivation of 2,1‐inserted (“dormant”) sites via chain transfer, rather than to (re)generation of active trivalent Ti via oxidative addition of hydrogen to divalent species. Decay in activity during polymerization was observed with both catalysts, indicating that for MgCl2/TiCl4 catalysts decay is not necessarily due to overreduction of Ti to the divalent state during polymerization. In ethylene polymerization both catalysts exhibited an acceleration rather than a decay profile. It is suggested that the observed decay in activity during propylene polymerization may be due to the formation of clustered species that are too hindered for propylene but that allow ethylene polymerization. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 2645–2652, 1997
  • Editor: New York: John Wiley & Sons, Inc
  • Idioma: Inglês
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