Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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Technical University of Denmark

in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (8/8 displayed)

  • 2021Toward a Design for Flowable and Extensible Ionomers: An Example of Diamine-Neutralized Entangled Poly(styrene-co-4-vinylbenzoic acid) Ionomer Melts17citations
  • 2020Linear Viscoelastic and Nonlinear Extensional Rheology of Diamine Neutralized Entangled Poly(styrene-co-4-vinylbenzoic acid) Ionomer Meltscitations
  • 2020Linear Viscoelastic and Nonlinear Extensional Rheology of Diamine Neutralized Entangled Poly(styrene-co-4-vinylbenzoic acid) Ionomer Meltscitations
  • 2020Threading-Unthreading Transition of Linear-Ring Polymer Blends in Extensional Flow43citations
  • 2019Molecular origin of strain hardening in blend of ring and linear polystyrenecitations
  • 2019Molecular origin of strain hardening in blend of ring and linear polystyrenecitations
  • 2019Rheological and mechanical properties of polystyrene with hydrogen bondingcitations
  • 2019Rheological and mechanical properties of polystyrene with hydrogen bondingcitations

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Chart of shared publication
Madsen, Jeppe
3 / 12 shared
Skov, Anne Ladegaard
4 / 298 shared
Genina, Natalja
3 / 8 shared
Madsen, Peter Jeppe
3 / 18 shared
Hassager, Ole
6 / 78 shared
Huang, Qian
5 / 25 shared
Skov, Anne L.
1 / 2 shared
Mortensen, Kell
3 / 24 shared
Vlassopoulos, Dimitris
3 / 24 shared
Borger, Anine
1 / 1 shared
Chang, Taihyun
3 / 11 shared
Oconnor, Thomas C.
1 / 1 shared
Jensen, Grethe
1 / 1 shared
Ge, Ting
1 / 2 shared
Ahn, Junyoung
3 / 9 shared
Grest, Gary S.
1 / 5 shared
Borger, Anine L.
2 / 5 shared
Jensen, Grethe V.
1 / 1 shared
Grethe, V. Jensen
1 / 1 shared
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2020
2019

Co-Authors (by relevance)

  • Madsen, Jeppe
  • Skov, Anne Ladegaard
  • Genina, Natalja
  • Madsen, Peter Jeppe
  • Hassager, Ole
  • Huang, Qian
  • Skov, Anne L.
  • Mortensen, Kell
  • Vlassopoulos, Dimitris
  • Borger, Anine
  • Chang, Taihyun
  • Oconnor, Thomas C.
  • Jensen, Grethe
  • Ge, Ting
  • Ahn, Junyoung
  • Grest, Gary S.
  • Borger, Anine L.
  • Jensen, Grethe V.
  • Grethe, V. Jensen
OrganizationsLocationPeople

document

Molecular origin of strain hardening in blend of ring and linear polystyrene

  • Wang, Wendi
  • Borger, Anine L.
  • Mortensen, Kell
  • Vlassopoulos, Dimitris
  • Chang, Taihyun
  • Ahn, Junyoung
  • Jensen, Grethe V.
Abstract

Ring polymers have attracted a great deal of scientific interest due to the lack of free ends which has dramatic consequences on their rheology. Previous studies show that the zero shear viscosity of pure rings is much lower than that of their linear counterparts with the same molecular weight.1 However, it has been shown that when linear polystyrene is mixed with rings in certain ratios, the zero shear viscosity of the blend is even higher than that of the linear. Uniaxial extensional rheology measurements of the blend show that the maximum stress was enhanced and followed by an unexpected stress overshoot at large Hencky strains. The strain hardening up until the maximum could be relevant e.g. for fiber spinning since strain hardening leads to increased molecular orientation and stretching that again leads to increased fiber strength. Ring linear blends may thus lead to stronger fibers in the future. In order to study the structural origin of the observed strain hardening, Very Small Angle Neutron Scattering (VSANS) is used in this study.<br/>In the present work, to explore how the rings affect the linear molecules, a blend of 30 % ring and 70 % linear polystyrene molecules (both of molecular weight 185 k and with 10 wt% deuterated linear chains) and a reference sample of pure linear polystyrene (also of molecular weight 185 k and 10 wt % deuterated chains) are used. The samples were prepared by using a filament stretching rheometer at 130oC with a constant Hencky strain rate of 0.003 s<sup>-1</sup>, and quenched at different times. One sample was quenched before the maximum stress where the segments start to be oriented. A second sample corresponds to maximum stress for the blend where the linear chains in the blend are stretched the most with respect to their counterparts in the pure linear. In this way, the level of molecular stretching of the linear component in the blend is quantified and compared with the linear material. Thus, we shine light on the origin of the strain hardening in the linear ring blend.

Topics
  • impedance spectroscopy
  • polymer
  • strength
  • viscosity
  • molecular weight
  • neutron scattering
  • spinning