A sensitive method to detect very low levels of long chain branching from the molar mass distribution and linear viscoelastic response

2005 ◽  
Vol 49 (6) ◽  
pp. 1503-1520 ◽  
Author(s):  
E. van Ruymbeke ◽  
V. Stéphenne ◽  
D. Daoust ◽  
P. Godard ◽  
R. Keunings ◽  
...  
2008 ◽  
Vol 48 (5) ◽  
pp. 479-490 ◽  
Author(s):  
Florian J. Stadler ◽  
Joachim Kaschta ◽  
Helmut Münstedt ◽  
Florian Becker ◽  
Michael Buback

Polymers ◽  
2021 ◽  
Vol 13 (3) ◽  
pp. 328
Author(s):  
Chuangbi Chen ◽  
Mehdihasan I. Shekh ◽  
Shuming Cui ◽  
Florian J. Stadler

Long-chain branched metallocene-catalyzed high-density polyethylenes (LCB-mHDPE) were solution blended to obtain blends with varying degrees of branching. A high molecular LCB-mHDPE was mixed with low molecular LCB-mHDPE at varying concentrations. The rheological behavior of those low molecular LCB-mHDPE is similar but their molar mass and molar mass distribution are significantly different. Those blends were characterized rheologically to study the effects of concentration, molar mass distribution, and long-chain branching level of the low molecular LCB-mHDPE. Owing to the ultra-long relaxation times of the high molecular LCB-mHDPE, the blends exhibited a clearly more long-chain branched behavior than the base materials. The thermorheological complexity analysis showed an apparent increase in the activation energies Ea determined from G′, G″, and especially δ. Ea(δ), which for LCB-mHDPE is a peak function, turned out to produce even more pronounced peaks than observed for LCB-mPE with narrow molar mass distribution and also LCB-mPE with broader molar mass distribution. Thus, it is possible to estimate the molar mass distribution from the details of the thermorheological complexity.


Author(s):  
Chuangbi Chen ◽  
Mehdihasan I. Shekh ◽  
Shuming Cui ◽  
Florian J. Stadler

Long-chain branched metallocene-catalyzed high-density polyethylenes (LCB-mHDPE) were solution blended to obtain blends with varying degrees of branching. A high molecular LCB-mHDPE was mixed with low molecular LCB-mHDPE are varying concentrations, whose rheological behavior is similar but whose molar mass and molar mass distribution is significantly different. Those blends were characterized rheologically to study the effects of concentration, molar mass distribution, and long-chain branching level of the low molecular LCB-mHDPE. Owing to the ultra-long relaxation times of the high molecular LCB-mHDPE, the blends started behaving clearly more long-chain branched than the base materials. The thermorheological complexity showed an apparent increase in the activation energies Ea determined from G’, G”, and especially δ. Ea(δ), which for LCB-mHDPE is a peak function, turned out to produce even more pronounced peaks than observed for regular LCB-mPE and also LCB-mPE with broader molar mass distribution. Thus, it is possible to estimate the molar mass distribution from the details of the thermorheological complexity.


Author(s):  
Chuangbi Chen ◽  
Mehdihasan I. Shekh ◽  
Shuming Cui ◽  
Florian J. Stadler

Long-chain branched metallocene-catalyzed high-density polyethylenes (LCB-mHDPE) were solution blended to obtain blends with varying degrees of branching. A high molecular LCB-mHDPE was mixed with low molecular LCB-mHDPE are varying concentrations, whose rheological behavior is similar but whose molar mass and molar mass distribution is significantly different. Those blends were characterized rheologically to study the effects of concentration, molar mass distribution, and long-chain branching level of the low molecular LCB-mHDPE. Owing to the ultra-long relaxation times of the high molecular LCB-mHDPE, the blends started behaving clearly more long-chain branched than the base materials. The thermorheological complexity showed an apparent increase in the activation energies Ea determined from G’, G”, and especially δ. Ea(δ), which for LCB-mHDPE is a peak function, turned out to produce even more pronounced peaks than observed for regular LCB-mPE and also LCB-mPE with broader molar mass distribution. Thus, it is possible to estimate the molar mass distribution from the details of the thermorheological complexity.


Polymers ◽  
2017 ◽  
Vol 9 (12) ◽  
pp. 442 ◽  
Author(s):  
Florian Kamleitner ◽  
Bernadette Duscher ◽  
Thomas Koch ◽  
Simone Knaus ◽  
Klaus Schmid ◽  
...  

Polymer ◽  
2004 ◽  
Vol 45 (8) ◽  
pp. 2803-2812 ◽  
Author(s):  
Chenyang Liu ◽  
Chaoxu Li ◽  
Peng Chen ◽  
Jiasong He ◽  
Qingrong Fan

2008 ◽  
Author(s):  
T. P. Karjala ◽  
R. L. Sammler ◽  
M. A. Mangnus ◽  
L. G. Hazlitt ◽  
M. S. Johnson ◽  
...  

2010 ◽  
Vol 119 (2) ◽  
pp. 636-646 ◽  
Author(s):  
Teresa P. Karjala ◽  
Robert L. Sammler ◽  
Marc A. Mangnus ◽  
Lonnie G. Hazlitt ◽  
Mark S. Johnson ◽  
...  

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