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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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (1/1 displayed)

  • 2022Cleavable epoxy networks using azomethine-bearing amine hardeners4citations

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Chart of shared publication
Weaver, Pm
1 / 560 shared
Manolakis, Ioannis
1 / 14 shared
Conaire, Marcus
1 / 1 shared
Chanteli, Angeliki
1 / 3 shared
Heise, Andreas
1 / 3 shared
Chart of publication period
2022

Co-Authors (by relevance)

  • Weaver, Pm
  • Manolakis, Ioannis
  • Conaire, Marcus
  • Chanteli, Angeliki
  • Heise, Andreas
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article

Cleavable epoxy networks using azomethine-bearing amine hardeners

  • Weaver, Pm
  • Manolakis, Ioannis
  • Conaire, Marcus
  • Brannigan, Ruairi
  • Chanteli, Angeliki
  • Heise, Andreas
Abstract

<p>This work is a proof-of-concept of the use of azomethine-bearing diamines as novel hardeners of standard epoxy compounds to yield cleavable and thermoformable covalent adaptable networks (CANs), with functional properties otherwise comparable to conventional epoxy networks. A suitable aromatic diamine (TPA-o-PD) was synthesised at acceptable purity for the intended use and successfully reacted with DGEBA. The resulting azomethine-bearing cured epoxy networks exhibited glass transition temperature values and a thermal stability profile similar to conventional epoxy network counterparts. In contrast to their conventional counterparts however, the azomethine-bearing networks were shown to dissolve in mixtures of chloroform and methanesulfonic acid, due to acid hydrolysis of at least some of the azomethine bonds of the network. The resulting recyclate material after evaporating the solvent was consistent with the profile of a thermoplastic polymer of high molecular weight, suggesting limited depolymerisation/network cleavage during dissolution in the chloroform/methanesulfonic acid mixture. The recyclates were soluble in polar aprotic solvents and showed good thermal stability, high T<sub>g</sub> and molecular weight values, consistent with the attributes of engineering thermoplastics. Lastly, the cured networks were shown to be thermoformable at 200 °C, yielding self-standing films with only minor reduction of properties.</p>

Topics
  • impedance spectroscopy
  • compound
  • glass
  • glass
  • glass transition temperature
  • molecular weight
  • thermoplastic
  • amine