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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Main Authors: Plog J. P., Kulicke W.-M., Clasen C.
Format: Article
Language:English
Published: De Gruyter 2005-02-01
Series:Applied Rheology
Subjects:
mwd
Online Access:https://doi.org/10.1515/arh-2005-0002
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spelling 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
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AT kulickewm influenceofthemolarmassdistributionontheelongationalbehaviourofpolymersolutionsincapillarybreakup
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