4.7 Article

Trouble-free combination of ?-alkenylmethyldichlorosilane copolymerization-hydrolysis chemistry and metallocene catalyst system for highly effective and efficient direct synthesis of long-chain-branched polypropylene

Journal

POLYMER
Volume 259, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.polymer.2022.125327

Keywords

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Funding

  1. National Natural Science Foundation of China
  2. [51973224]
  3. [52173013]

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This paper reports a highly effective and efficient synthesis of long-chain-branched polypropylene (LCB-PP) using ACH chemistry and metallocene catalyst system. The synthesized LCB-PPs have narrow molecular weight distribution and well-defined structure. This method is simpler and more efficient compared to two other existing methods.
This paper reports a highly effective and efficient synthesis of long-chain-branched polypropylene (LCB-PP) rendered by combination of w-alkenylmethyldi-chlorosilane copolymerization-hydrolysis (ACH) chemistry and metallocene catalyst system. The potential side reaction, the dichlorosilane-methylaluminoxane (MAO) double replacement reaction, is revealed to be slow-occurring and largely suppressible by slightly increasing the steric hindrance of the alkyl substituent (s) on the reactants. Thus, with 5-hexenylmethyldichlorosilane and 7-octenylmethyldichlorosilane of some increased alkenyl chain lengths, the main/side reaction competition dynamics in w-alkenylmethyldichlorosilane/propylene copolymerization with metallocene (rac-Me2Si-[2-Me-4-Ph(Ind)]2ZrCl2)-modified MAO complex involving the dichlorosilane-MAO double replacement reaction could shift disproportionally to the main copolymerization to the extent that the effect of the side reaction is not detectable. The synthesized LCB-PPs are characterized by narrow molecular weight distribution, with the LCB structure being H-shape and the interlinkage well defined as 1,2-dihydroxylsiloxane. The successful combination of ACH chemistry and metallocene catalyst system based on conventional metal-locene and MAO assures a facile, well-defined, and, most importantly, highly effective and efficient synthesis of H-shape LCB-PP, as compared to two existing outstanding chemistries rendering the same type of LCB-PP, including ACH chemistry combined with heterogeneous Ziegler-Natta catalyst system and nonconjugated a,w-diolefin copolymerization (NDC) chemistry exercised with 1,9-decadiene and metallocene catalyst system.

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