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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Natália, T. Correia

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Université de Lille

in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (7/7 displayed)

  • 2021How Molecular Mobility, Physical State, and Drug Distribution Influence the Naproxen Release Profile from Different Mesoporous Silica Matrices5citations
  • 2021Interactions underpinning the plasticization of a polymer matrix: a dynamic and structural analysis of DMP-plasticized cellulose acetate17citations
  • 2021Impact of chirality in the amorphous state of conglomerate forming systems: case study of N-acetyl-α-methylbenzylamine4citations
  • 2017Interactions underpinning the plasticization of a polymer matrix: a dynamic and structural analysis of DMP-plasticized cellulose acetate17citations
  • 2012Understanding the Ion Jelly Conductivity Mechanism26citations
  • 2011Molecular dynamics of poly(ATRIF) homopolymer and poly(AN-co-ATRIF) copolymer investigated by dielectric relaxation spectroscopy21citations
  • 2011Phase Transformations Undergone by Triton X-100 Probed by Differential Scanning Calorimetry and Dielectric Relaxation Spectroscopy17citations

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Dorey, Piedade
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Lourenço, Mirtha A. O.
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Danède, Florence
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Sotomayor, João C.
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Sotomayor, Joao
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Co-Authors (by relevance)

  • Dorey, Piedade
  • Lourenço, Mirtha A. O.
  • Danède, Florence
  • Ferreira, Paula
  • Sotomayor, João C.
  • Dionísio, Madalena
  • Cordeiro, Teresa
  • Matos, Inês
  • Fonseca, Isabel M.
  • Aubry, Jean-Marie
  • Molinier, Valérie
  • Descamps, Marc
  • Dudognon, Emeline
  • Benazzouz, Adrien
  • Coquerel, Gérard
  • Affouard, Frederic
  • Couvrat, Nicolas
  • Saiter, Allisson
  • Atawa, Bienvenu
  • Dias, Carlos
  • Barreiros, Susana
  • Andrade, Maria Madalena Dionísio
  • Cabrita, Eurico J.
  • Sotomayor, Joao
OrganizationsLocationPeople

article

Molecular dynamics of poly(ATRIF) homopolymer and poly(AN-co-ATRIF) copolymer investigated by dielectric relaxation spectroscopy

  • Andrade, Maria Madalena Dionísio
  • Natália, T. Correia
Abstract

Aiming to develop new dielectric polymers containing CN and F groups with strong dipole moments, a novel copolymer of acrylonitrile (AN) and 2,2,2-trifluoroethyl acrylate (ATRIF) was synthesized in acetonitrile by free radical process as well as the respective homopolymer (poly(ATRIF)). The copolymer's composition and microstructure were analyzed by FTIR, (1)H and (13)C NMR spectroscopy and SEC. The molar incorporation of AN determined in the copolymer by NMR was 58 mol%. Thermogravimetric analysis of poly(AN-co-ATRIF) copolymer showed good thermal stability comparatively to the fluorinated homopolymer. Both copolymer, poly(AN-co-ATRIF), and homopolymer, poly(ATRIF), were dielectrically characterized over a frequency range from 10(-1) to 10(6) Hz, and in a temperature range from 223 to 393 K. The dominating relaxation process detected in both materials is the alpha-relaxation, associated with the dynamic glass transition. A VFTH temperature dependence of the relaxation times (tau) was found for both materials, as characteristic of cooperative processes, from which the respective glass transition temperatures (T(g)(tau = 100 s)) were estimated, which differ similar to 40 K, the one of the copolymer being higher (307 K) in accordance to the calorimetric analysis. This effect was attributed to a higher stiffness of the backbone in the copolymer originated by the inclusion of the acrylonitrile groups. Both relaxation functions have the same breath of relaxation times allowing constructing a single master curve, indicating similar non-exponential character. A less fragile behavior was found for the copolymer. This was rationalized in a more straightforward way by the free volume approach instead from a correlation between fragility and intermolecular coupling. It was found that in the copolymer the free volume increases at a lower rate with the temperature increase. It was inferred from the VFTH temperature dependence of the dc conductivity and low values of the decoupling index that ion motion is significantly influenced by the dynamics of the alpha-process. <br/>

Topics
  • impedance spectroscopy
  • microstructure
  • inclusion
  • glass
  • glass
  • molecular dynamics
  • laser emission spectroscopy
  • thermogravimetry
  • glass transition temperature
  • copolymer
  • size-exclusion chromatography
  • homopolymer
  • Nuclear Magnetic Resonance spectroscopy