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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1.080 Topics available

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693.932 PEOPLE
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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (4/4 displayed)

  • 2024Composition-dependent morphologies of CeO2 nanoparticles in the presence of Co-adsorbed H2O and CO28citations
  • 2024Composition-dependent morphologies of CeO 2 nanoparticles in the presence of Co-adsorbed H 2 O and CO 2 : a density functional theory study8citations
  • 2023Agarose Fluid Gels Formed by Shear Processing During Gelation for Suspended 3D Bioprinting6citations
  • 2022Structure and Properties of Cubic PuH2 and PuH34citations

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Chart of shared publication
Parker, Stephen C.
2 / 33 shared
Gillie, Lisa
2 / 6 shared
Flitcroft, Joseph M.
2 / 2 shared
Molinari, Marco
3 / 17 shared
Cooke, David
2 / 5 shared
Symington, Adam R.
2 / 3 shared
Tse, Joshua S.
2 / 2 shared
Skelton, Jonathan M.
2 / 30 shared
Gillie, Lisa J.
1 / 1 shared
Cooke, David J.
1 / 1 shared
Senior, Jessica
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Cooke, Megan E.
1 / 2 shared
Moakes, Richard J. A.
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Grover, Liam M.
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Smith, Alan
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Harker, Robert M.
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Smith, Thomas
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Silva, Estelina Lora Da
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Storr, Mark T.
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Co-Authors (by relevance)

  • Parker, Stephen C.
  • Gillie, Lisa
  • Flitcroft, Joseph M.
  • Molinari, Marco
  • Cooke, David
  • Symington, Adam R.
  • Tse, Joshua S.
  • Skelton, Jonathan M.
  • Gillie, Lisa J.
  • Cooke, David J.
  • Senior, Jessica
  • Cooke, Megan E.
  • Moakes, Richard J. A.
  • Grover, Liam M.
  • Smith, Alan
  • Harker, Robert M.
  • Smith, Thomas
  • Silva, Estelina Lora Da
  • Storr, Mark T.
OrganizationsLocationPeople

article

Agarose Fluid Gels Formed by Shear Processing During Gelation for Suspended 3D Bioprinting

  • Senior, Jessica
  • Cooke, Megan E.
  • Moxon, Samuel
  • Moakes, Richard J. A.
  • Grover, Liam M.
  • Smith, Alan
Abstract

<p>The use of granular matrices to support parts during the bioprinting process was first reported by Bhattacharjee et al. in 2015, and since then, several approaches have been developed for the preparation and use of supporting gel beds in 3D bioprinting. This paper describes a process to manufacture microgel suspensions using agarose (known as fluid gels), wherein particle formation is governed by the application of shear during gelation. Such processing produces carefully defined microstructures, with subsequent material properties that impart distinct advantages as embedding print media, both chemically and mechanically. These include behaving as viscoelastic solid-like materials at zero shear, limiting long-range diffusion, and demonstrating the characteristic shear-thinning behavior of flocculated systems. On the removal of shear stress, however, fluid gels have the capacity to rapidly recover their elastic properties. This lack of hysteresis is directly linked to the defined microstructures previously alluded to; because of the processing, reactive, non-gelled polymer chains at the particle interface facilitate interparticle interactions-similar to a Velcro effect. This rapid recovery of elastic properties enables bioprinting high-resolution parts from low-viscosity biomaterials, as rapid reformation of the support bed traps the bioink in situ, maintaining its shape. Furthermore, an advantage of agarose fluid gels is the asymmetric gelling/melting transitions (gelation temperature of ~30 °C and melting temperature of ~90 °C). This thermal hysteresis of agarose makes it possible to print and culture the bioprinted part in situ without the supporting fluid gel melting. This protocol shows how to manufacture agarose fluid gels and demonstrates their use to support the production of a range of complex hydrogel parts within suspended-layer additive manufacture (SLAM).</p>

Topics
  • impedance spectroscopy
  • microstructure
  • polymer
  • reactive
  • viscosity
  • biomaterials
  • melting temperature
  • gelation