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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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (2/2 displayed)

  • 2010Hydrogels from ABA and ABC triblock polymers82citations
  • 2010Self-assembly of fibronectin mimetic peptide-amphiphile nanofibers76citations

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Chart of shared publication
Tsapatsis, Michael
1 / 3 shared
Fan, Wei
1 / 9 shared
Kokkoli, Efrosini
1 / 2 shared
Rexeisen, Emilie L.
1 / 1 shared
Bates, Frank S.
1 / 90 shared
Pangburn, Todd O.
1 / 1 shared
Chart of publication period
2010

Co-Authors (by relevance)

  • Tsapatsis, Michael
  • Fan, Wei
  • Kokkoli, Efrosini
  • Rexeisen, Emilie L.
  • Bates, Frank S.
  • Pangburn, Todd O.
OrganizationsLocationPeople

article

Hydrogels from ABA and ABC triblock polymers

  • Taribagil, Rajiv R.
Abstract

<p>Aqueous gels of telechelic poly(ethylene oxide) (PEO)-based triblock polymers, with homo and hetero combinations of 1,2-polybutadiene (PB) and poly(perfluoropropylene oxide) (PFPO) as hydrophobic end-blocks, were prepared by anionic polymerization and polymer - polymer coupling reactions. The block molecular weights in kg/mol were (2.7 - 24 - 2.7) for PB-b-PEO-b-PB, (2.3 - 23 - 2.3) for PFPO-b-PEO-b-PFPO, and (1.9 - 26 - 2.3) for PB-b-PEO-b-PFPO. Gels with polymer concentrations ranging from 10 to 50 wt % were investigated using cryogenic scanning electron microscopy (cryo-SEM) and small-angle neutron scattering (SANS). The cryo-SEM micrographs revealed significant differences among the morphologies of the gels obtained, depending on the end-blocks used. Results from contrast matching SANS experiments were used to corroborate and refine the information obtained from microscopy. The PB-b-PEO-b-PB copolymers formed networks of spherical micelles at all concentrations as expected, albeit with significant spatial heterogeneity that diminished with increasing concentration. The PFPO-b-PEO-b-PFPO copolymers also formed networks by aggregation of the end-blocks, but the PFPO blocks tended to adopt disklike or even sheetlike structures. This is attributed to the extremely high interfacial tension of PFPO with water and is consistent with the super-strong segregation regime behavior. The heterotelechelic PB-b-PEO-b-PFPO terpolymers adopted a quite different structure, namely an intricate bicontinuous open-cell foam, with cells on the order of 500 nm in size and cell walls composed of PFPO disks embedded in PB sheets. These various network structures illustrate the potential of using end-block chemistry to manipulate both the morphology and the physical properties of polymer gels.</p>

Topics
  • impedance spectroscopy
  • morphology
  • scanning electron microscopy
  • experiment
  • interfacial
  • molecular weight
  • copolymer
  • small-angle neutron scattering