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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Materials Map under construction

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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Jensen, Grethe Vestergaard

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (4/4 displayed)

  • 2023Aggregative adherence fimbriae form compact structures as seen by SAXS3citations
  • 2020Dispersion state of TiO2 pigment particles studied by ultra-small-angle X-ray scattering revealing dependence on dispersant but limited change during drying of paint coating22citations
  • 2014The mixture of poly(propylene-glycol)-block-poly(ethylene-glycol)-block-PPG with C 12 E 5 microemulsion9citations
  • 2011Structure of PEP-PEO block copolymer micelles: Exploiting the complementarity of small-angle X-ray scattering and static light scattering17citations

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Jenssen, Håvard
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Björling, Alexander
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Skar-Gislinge, Nicholas
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Arleth, Lise
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Jønsson, Rie
1 / 1 shared
Midtgaard, Søren Roi
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Krogfelt, Karen Angeliki
1 / 1 shared
Matthews, Steve
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Parasida, Claire F.
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Kynde, Soren
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Midtgaard, Soren R.
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Zalich, Michael
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Ducher, Pascal
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Lof, David
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Hamieau, Guillaume
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Sharifi, Soheil
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Pedersen, Jan Skov
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Marti, Othmar
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Amirkhani, Masoud
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Shi, Qing
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Oliveira, Cristiano L. P.
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Hernansanz, Maria J.
1 / 1 shared
Deen, G. Roshan
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Almdal, Kristoffer
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Co-Authors (by relevance)

  • Jenssen, Håvard
  • Björling, Alexander
  • Skar-Gislinge, Nicholas
  • Arleth, Lise
  • Jønsson, Rie
  • Midtgaard, Søren Roi
  • Krogfelt, Karen Angeliki
  • Matthews, Steve
  • Parasida, Claire F.
  • Kynde, Soren
  • Midtgaard, Soren R.
  • Zalich, Michael
  • Ducher, Pascal
  • Lof, David
  • Hamieau, Guillaume
  • Sharifi, Soheil
  • Pedersen, Jan Skov
  • Marti, Othmar
  • Amirkhani, Masoud
  • Shi, Qing
  • Oliveira, Cristiano L. P.
  • Hernansanz, Maria J.
  • Deen, G. Roshan
  • Almdal, Kristoffer
OrganizationsLocationPeople

article

Structure of PEP-PEO block copolymer micelles: Exploiting the complementarity of small-angle X-ray scattering and static light scattering

  • Pedersen, Jan Skov
  • Shi, Qing
  • Oliveira, Cristiano L. P.
  • Hernansanz, Maria J.
  • Jensen, Grethe Vestergaard
  • Deen, G. Roshan
  • Almdal, Kristoffer
Abstract

The structure of large block copolymer micelles is traditionally determined by small-angle neutron scattering (SANS), covering a large range of scattering vectors and employing contrast variation to determine the overall micelle morphology as well as the internal structure on shorter length scales. The present work shows that the same information can be obtained by combining static light scattering (SLS) and small-angle X-ray scattering (SAXS), which provide information on, respectively, large and short length scales. Micelles of a series of block copolymers of poly(ethylene propylene)-b-poly(ethylene oxide) (PEP-PEO) in a 70% ethanol solution are investigated. The polymers have identical PEP blocks of 5.0 kDa and varying PEO blocks of 2.8-49 kDa. The SLS contrasts of PEP and PEO are similar, providing a homogeneous contrast, making SLS ideal for determining the overall micelle morphology. The SAXS contrasts of the two components are very different, allowing for resolution of the internal micelle structure. A core-shell model with a PEP core and PEO corona is fitted simultaneously to the SAXS and SLS data using the different contrasts of the two blocks for each technique. With increasing PEO molecular weight, a transition from cylindrical to spherical micelles is observed. This transition cannot be identified from the SAXS data alone, but only from the SLS data.

Topics
  • impedance spectroscopy
  • morphology
  • molecular weight
  • copolymer
  • block copolymer
  • small-angle neutron scattering
  • small angle x-ray scattering
  • static light scattering