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Synthesis and Microstructurral Study of Stereoblock Elastomeric Polypropylenes from Metallocene Catalyst (2-PhInd)2ZrCl2 Activated with Cocatalyst Mixtures

نویسنده:
G. H. Nejabat
,
M. Nekoomanesh
,
H. Arabi
,
H. Salehi-Mobarakeh
,
غلامحسین ظهوری
,
M. Omidvar
,
S. A. Miller
,
Gholamhossein Zohuri
سال
: 2013
چکیده: Various elastomeric polypropylenes (PPs) are synthe-

sized through homogeneous propylene polymerization with met-

allocene catalyst (2-PhInd)2ZrCl2 in the presence of different

cocatalyst mixtures: triethylaluminum (TEA)/methylaluminoxane

(MAO) or triisobutylaluminum (TIBA)/MAO in the range of AlAlR3/

AlMAO ¼ 0.0–0.9. The cocatalyst formulation impacts the resultant

polymer microstructure and the thermal and dynamic mechanical

properties of the produced PPs.

13

C NMR analysis of the polymers

reveals essentially atactic PP, with mmmm ¼ 7.9%, when AlAlR3/

AlMAO ¼ 0.0. The mmmm pentad content is maximized when

AlAlR3/AlMAO ¼ 0.8; for TIBA, mmmm ¼ 23.5%; and for TEA,

mmmm ¼ 17.6%. Differential scanning calorimetry analysis and

dynamic mechanical thermal analysis corroborate these findings.

Specifically, Tm, DHm,and Tg are essentially maximized under

these conditions, and the minimum damping is observed for

AlAlR3/AlMAO ¼ 0.6–0.8.

1

H NMR analysis of themixtures of catalyst

and cocatalysts (without monomer) shows very minor differences

for [Zr]:AlAlR3 in the range of 1:1–1:5.V C 2012Wiley Periodicals, Inc.

J. Polym. Sci., Part A: Polym. Chem. 2013, 51,724–731
یو آر آی: http://libsearch.um.ac.ir:80/fum/handle/fum/3345234
کلیدواژه(گان): catalysts,elastomers,metallocene catalysts,polyolefins,poly(propylene) (PP)
کالکشن :
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    Synthesis and Microstructurral Study of Stereoblock Elastomeric Polypropylenes from Metallocene Catalyst (2-PhInd)2ZrCl2 Activated with Cocatalyst Mixtures

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contributor authorG. H. Nejabaten
contributor authorM. Nekoomaneshen
contributor authorH. Arabien
contributor authorH. Salehi-Mobarakehen
contributor authorغلامحسین ظهوریen
contributor authorM. Omidvaren
contributor authorS. A. Milleren
contributor authorGholamhossein Zohurifa
date accessioned2020-06-06T13:11:27Z
date available2020-06-06T13:11:27Z
date issued2013
identifier urihttp://libsearch.um.ac.ir:80/fum/handle/fum/3345234?locale-attribute=fa
description abstractVarious elastomeric polypropylenes (PPs) are synthe-

sized through homogeneous propylene polymerization with met-

allocene catalyst (2-PhInd)2ZrCl2 in the presence of different

cocatalyst mixtures: triethylaluminum (TEA)/methylaluminoxane

(MAO) or triisobutylaluminum (TIBA)/MAO in the range of AlAlR3/

AlMAO ¼ 0.0–0.9. The cocatalyst formulation impacts the resultant

polymer microstructure and the thermal and dynamic mechanical

properties of the produced PPs.

13

C NMR analysis of the polymers

reveals essentially atactic PP, with mmmm ¼ 7.9%, when AlAlR3/

AlMAO ¼ 0.0. The mmmm pentad content is maximized when

AlAlR3/AlMAO ¼ 0.8; for TIBA, mmmm ¼ 23.5%; and for TEA,

mmmm ¼ 17.6%. Differential scanning calorimetry analysis and

dynamic mechanical thermal analysis corroborate these findings.

Specifically, Tm, DHm,and Tg are essentially maximized under

these conditions, and the minimum damping is observed for

AlAlR3/AlMAO ¼ 0.6–0.8.

1

H NMR analysis of themixtures of catalyst

and cocatalysts (without monomer) shows very minor differences

for [Zr]:AlAlR3 in the range of 1:1–1:5.V C 2012Wiley Periodicals, Inc.

J. Polym. Sci., Part A: Polym. Chem. 2013, 51,724–731
en
languageEnglish
titleSynthesis and Microstructurral Study of Stereoblock Elastomeric Polypropylenes from Metallocene Catalyst (2-PhInd)2ZrCl2 Activated with Cocatalyst Mixturesen
typeJournal Paper
contenttypeExternal Fulltext
subject keywordscatalystsen
subject keywordselastomersen
subject keywordsmetallocene catalystsen
subject keywordspolyolefinsen
subject keywordspoly(propylene) (PP)en
journal titleJournal of Polymer Science, Part A: Polymer Chemistryfa
pages724-731
journal volume51
journal issue51
identifier linkhttps://profdoc.um.ac.ir/paper-abstract-1032609.html
identifier articleid1032609
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