Materials Map

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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%

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Publications (1/1 displayed)

  • 2014Physicomechanical characterization of monodisperse multivesiculated polyester particles5citations

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Mendes, Am
1 / 12 shared
Magalhaes, Fd
1 / 12 shared
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2014

Co-Authors (by relevance)

  • Mendes, Am
  • Magalhaes, Fd
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article

Physicomechanical characterization of monodisperse multivesiculated polyester particles

  • Mendes, Am
  • Magalhaes, Fd
  • Fidalgo, J.
Abstract

This work describes physicomechanical properties of low-density polyester particles with multi-alveolar inner morphology, obtained via a water/oil/water double emulsion process. Monodisperse particle diameters were produced thanks to the use of a microchannel T-junction device for droplet generation. The drying conditions tested showed that rapid water evaporation at 120 degrees C, combined with slow diffusion towards the exterior, causes internal fracture and particle deformation. Interestingly, all particles present virtually identical internal damage and external deformation features under these drying conditions, demonstrating the uniformity in internal structures. Drying at 70 degrees C allows for efficient water removal with no damage. Thermomechanical transitions and thermal stability were analyzed by dynamic mechanical analysis (DMA in single-particle compression mode), dynamic scanning calorimetry (DSC) and thermogravimetry (TG). The effectiveness of curing conditions was evaluated by FTIR and DSC, allowing to identify the need of a thermal post-treatment for consumption of residual styrene. The consequent increase in degree of crosslinking produced a positive shift in glass transition temperature measured by DMA. Finally, mechanical reinforcement of the multivesiculated polyester particles was obtained by loading the polymer with surface-modified fumed silica, yielding 75% increase in storage modulus.

Topics
  • density
  • surface
  • polymer
  • glass
  • glass
  • thermogravimetry
  • glass transition temperature
  • differential scanning calorimetry
  • evaporation
  • drying
  • curing
  • dynamic mechanical analysis
  • dynamic scanning calorimetry