Influence of the Molar Mass Distribution on the Elongational Behaviour of Polymer Solutions in Capillary Breakup
Commercially available, blended methylhydroxyethyl celluloses with similar weight-average molar masses but varying molar mass distributions were characterized by different techniques like steady shear flow and uniaxial elongation in capillary breakup experiments. The determined relaxation times t we...
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2005-02-01
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Online Access: | https://doi.org/10.1515/arh-2005-0002 |
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doaj-9f1022f30fe140df95b1c73c812773de2021-09-06T19:40:00ZengDe GruyterApplied Rheology1617-81062005-02-01151283710.1515/arh-2005-0002Influence of the Molar Mass Distribution on the Elongational Behaviour of Polymer Solutions in Capillary BreakupPlog J. P.0Kulicke W.-M.1Clasen C.2Institute for Technical and Macromoleculare Chemistry, University of Hamburg, Bundesstr. 45, 20146Hamburg, GermanyInstitute for Technical and Macromoleculare Chemistry, University of Hamburg, Bundesstr. 45, 20146Hamburg, GermanyInstitute for Technical and Macromoleculare Chemistry, University of Hamburg, Bundesstr. 45, 20146Hamburg, GermanyCommercially available, blended methylhydroxyethyl celluloses with similar weight-average molar masses but varying molar mass distributions were characterized by different techniques like steady shear flow and uniaxial elongation in capillary breakup experiments. The determined relaxation times t were then correlated with the absolute molar mass distribution acquired via SEC/MALLS/DRI (combined methods of size-exclusion-chromatography, multi angle laser light scattering and differential refractometer). In order to describe the longest relaxation time of the polymers in uniaxial elongation via integral mean values of the molar mass distribution, defined blends of polystyrene standards with varying molar mass distributions were characterized. The obtained data was scaled via different moments of the molecular weight distribution and could be correlated with the results obtained for the methylhydroxyethyl celluloses.https://doi.org/10.1515/arh-2005-0002elongational rheologypolystyrene blendsmhecmwd |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Plog J. P. Kulicke W.-M. Clasen C. |
spellingShingle |
Plog J. P. Kulicke W.-M. Clasen C. Influence of the Molar Mass Distribution on the Elongational Behaviour of Polymer Solutions in Capillary Breakup Applied Rheology elongational rheology polystyrene blends mhec mwd |
author_facet |
Plog J. P. Kulicke W.-M. Clasen C. |
author_sort |
Plog J. P. |
title |
Influence of the Molar Mass Distribution on the Elongational Behaviour of Polymer Solutions in Capillary Breakup |
title_short |
Influence of the Molar Mass Distribution on the Elongational Behaviour of Polymer Solutions in Capillary Breakup |
title_full |
Influence of the Molar Mass Distribution on the Elongational Behaviour of Polymer Solutions in Capillary Breakup |
title_fullStr |
Influence of the Molar Mass Distribution on the Elongational Behaviour of Polymer Solutions in Capillary Breakup |
title_full_unstemmed |
Influence of the Molar Mass Distribution on the Elongational Behaviour of Polymer Solutions in Capillary Breakup |
title_sort |
influence of the molar mass distribution on the elongational behaviour of polymer solutions in capillary breakup |
publisher |
De Gruyter |
series |
Applied Rheology |
issn |
1617-8106 |
publishDate |
2005-02-01 |
description |
Commercially available, blended methylhydroxyethyl celluloses with similar weight-average molar masses but varying molar mass distributions were characterized by different techniques like steady shear flow and uniaxial elongation in capillary breakup experiments. The determined relaxation times t were then correlated with the absolute molar mass distribution acquired via SEC/MALLS/DRI (combined methods of size-exclusion-chromatography, multi angle laser light scattering and differential refractometer). In order to describe the longest relaxation time of the polymers in uniaxial elongation via integral mean values of the molar mass distribution, defined blends of polystyrene standards with varying molar mass distributions were characterized. The obtained data was scaled via different moments of the molecular weight distribution and could be correlated with the results obtained for the methylhydroxyethyl celluloses. |
topic |
elongational rheology polystyrene blends mhec mwd |
url |
https://doi.org/10.1515/arh-2005-0002 |
work_keys_str_mv |
AT plogjp influenceofthemolarmassdistributionontheelongationalbehaviourofpolymersolutionsincapillarybreakup AT kulickewm influenceofthemolarmassdistributionontheelongationalbehaviourofpolymersolutionsincapillarybreakup AT clasenc influenceofthemolarmassdistributionontheelongationalbehaviourofpolymersolutionsincapillarybreakup |
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1717769583520120832 |