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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977 Locations available

693.932 PEOPLE
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Hennessy, Mg

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University of Bristol

in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (8/8 displayed)

  • 2023The dynamics of a collapsing polyelectrolyte gel4citations
  • 2020Phonon hydrodynamics in frequency-domain thermoreflectance experiments42citations
  • 2020Phase separation in swelling and deswelling hydrogels with a free boundary22citations
  • 2017Monomer diffusion into static and evolving polymer networks during frontal photopolymerisation14citations
  • 2016Surface waves on a soft viscoelastic layer produced by an oscillating microbubble9citations
  • 2015Controlling frontal photopolymerization with optical attenuation and mass diffusion21citations
  • 2015Controlled topological transitions in thin-film phase separation2citations
  • 2014Propagating topological transformations in thin immiscible bilayer films5citations

Places of action

Chart of shared publication
Münch, A.
1 / 4 shared
Wagner, Barbara
4 / 32 shared
Celora, Gl
1 / 1 shared
Waters, Sl
1 / 1 shared
Sendra, L.
1 / 2 shared
Alvarez, F. X.
1 / 1 shared
Myers, T. G.
1 / 2 shared
Beardo, A.
1 / 2 shared
Bafaluy, J.
1 / 2 shared
Camacho, J.
1 / 2 shared
Münch, Andreas
3 / 29 shared
Vitale, Alessandra
2 / 15 shared
Matar, Omar K.
3 / 6 shared
Cabral, João T.
2 / 3 shared
Pommella, Angelo
1 / 1 shared
Tinguely, Marc
1 / 1 shared
Garbin, Valeria
1 / 2 shared
Burlakov, Victor M.
2 / 5 shared
Goriely, Alain
2 / 8 shared
Chart of publication period
2023
2020
2017
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Co-Authors (by relevance)

  • Münch, A.
  • Wagner, Barbara
  • Celora, Gl
  • Waters, Sl
  • Sendra, L.
  • Alvarez, F. X.
  • Myers, T. G.
  • Beardo, A.
  • Bafaluy, J.
  • Camacho, J.
  • Münch, Andreas
  • Vitale, Alessandra
  • Matar, Omar K.
  • Cabral, João T.
  • Pommella, Angelo
  • Tinguely, Marc
  • Garbin, Valeria
  • Burlakov, Victor M.
  • Goriely, Alain
OrganizationsLocationPeople

article

Controlling frontal photopolymerization with optical attenuation and mass diffusion

  • Vitale, Alessandra
  • Hennessy, Mg
  • Matar, Omar K.
  • Cabral, João T.
Abstract

Frontal photopolymerization (FPP) is a versatile directional solidification process that can be used to rapidly fabricate polymer network materials by selectively exposing a photosensitive monomer bath to light. A characteristic feature of FPP is that the monomer-to-polymer conversion profiles take on the form of traveling waves that propagate into the unpolymerized bulk from the illuminated surface. Practical implementations of FPP require detailed knowledge about the conversion profile and speed of these traveling waves. The purpose of this theoretical study is to (i) determine the conditions under which FPP occurs and (ii) explore how optical attenuation and mass transport can be used to finely tune the conversion profile and propagation kinetics. Our findings quantify the strong optical attenuation and slow mass transport relative to the rate of polymerization required for FPP. The shape of the traveling wave is primarily controlled by the magnitude of the optical attenuation coefficients of the neat and polymerized material. Unexpectedly, we find that mass diffusion can increase the net extent of polymerization and accelerate the growth of the solid network. The theoretical predictions are found to be in excellent agreement with experimental data acquired for representative systems.

Topics
  • impedance spectroscopy
  • surface
  • polymer
  • directional solidification