Chemical composition distribution study in ethylene/1‐hexene copolymerization to produce LLDPE material using MgCl 2 ‐TiCl 4 ‐based Ziegler‐Natta catalysts

The characteristic features of LLDPE polymerization with ZN catalyst are the time drift effect during polymerization and the bending effect when trying to decrease density of the copolymer by adding more comonomer to the polymerization. The time drift in LLDPE polymerization is revealed by a constan...

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Veröffentlicht in:Journal of applied polymer science 2010-01, Vol.115 (2), p.826-836
Hauptverfasser: Garoff, Thomas, Mannonen, Laura, Väänänen, Marjo, Eriksson, Virgine, Kallio, Kalle, Waldvogel, Päivi
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container_issue 2
container_start_page 826
container_title Journal of applied polymer science
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creator Garoff, Thomas
Mannonen, Laura
Väänänen, Marjo
Eriksson, Virgine
Kallio, Kalle
Waldvogel, Päivi
description The characteristic features of LLDPE polymerization with ZN catalyst are the time drift effect during polymerization and the bending effect when trying to decrease density of the copolymer by adding more comonomer to the polymerization. The time drift in LLDPE polymerization is revealed by a constant decrease of comonomer incorporation during polymerization time. The bending is revealed by difficulties in lowering the density of LLDPE material below the density of 920 kg/m 3 . With increasing comonomer content during polymerization, the density does not decrease, but the soluble fraction increases. To try to observe if these phenomena are connected, two types of catalysts, SiO 2 supported and precipitated MgCl 2 ZN catalysts, were studied. A short time (10 min) and an extended time (60 min) copolymerization test series where the polymerizations were performed in the presence of a gradually increasing comonomer amount. Both catalysts show a strong bending when density is presented as a function of 1‐hexene both in 10‐ and 60‐min polymerization, indicating no connection between time drift and bending. The density, melting point, and crystallinity results all indicate that both catalysts are making similar copolymer material with identical chemical composition distribution. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010
doi_str_mv 10.1002/app.29701
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The time drift in LLDPE polymerization is revealed by a constant decrease of comonomer incorporation during polymerization time. The bending is revealed by difficulties in lowering the density of LLDPE material below the density of 920 kg/m 3 . With increasing comonomer content during polymerization, the density does not decrease, but the soluble fraction increases. To try to observe if these phenomena are connected, two types of catalysts, SiO 2 supported and precipitated MgCl 2 ZN catalysts, were studied. A short time (10 min) and an extended time (60 min) copolymerization test series where the polymerizations were performed in the presence of a gradually increasing comonomer amount. Both catalysts show a strong bending when density is presented as a function of 1‐hexene both in 10‐ and 60‐min polymerization, indicating no connection between time drift and bending. 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title Chemical composition distribution study in ethylene/1‐hexene copolymerization to produce LLDPE material using MgCl 2 ‐TiCl 4 ‐based Ziegler‐Natta catalysts
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