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%

Topics

Publications (2/2 displayed)

  • 2020Dilute Solution Properties of Poly(benzyl methacrylate) in Ionic Liquids17citations
  • 2017Coil Dimensions of Poly(ethylene oxide) in an Ionic Liquid by Small-Angle Neutron Scattering27citations

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Stepanek, Petr
1 / 6 shared
Černoch, Peter
1 / 2 shared
Hall, Cecilia
1 / 1 shared
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2020
2017

Co-Authors (by relevance)

  • Stepanek, Petr
  • Černoch, Peter
  • Hall, Cecilia
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article

Dilute Solution Properties of Poly(benzyl methacrylate) in Ionic Liquids

  • Stepanek, Petr
  • Černoch, Peter
  • Kharel, Aakriti
  • Hall, Cecilia
Abstract

<p>The static and dynamic properties of a range of molecular weights (2 × 10<sup>4</sup> to 1.6 × 10<sup>5</sup> g/mol) of poly(benzyl methacrylate) have been assessed in four different imidazolium- A nd pyrrolidinium-based ionic liquids over a wide temperature range (27-155 °C), primarily using light scattering techniques. All four systems exhibit lower critical solution temperature phase behavior. The relevant structural, dynamic, and thermodynamic parameters were examined as a function of concentration, temperature, and molecular weight. Some interesting observations were revealed. The phase boundaries suggest a shift of the critical composition toward the polymer-rich region, in contrast to the low critical concentrations for polymers commonly observed in polymer solutions. Surprisingly, the second virial coefficient (A<sub>2</sub>) remains positive, even at temperatures close to phase separation, where A<sub>2</sub> &lt; 0 is anticipated. Furthermore, A<sub>2</sub> also shows stronger dependence on molecular weight than commonly observed for polymers in good solvents. On the dynamic side, the diffusion virial coefficients (k<sub>d</sub>) remained positive over the given temperature range, further corroborating the apparent good solvent behavior of A<sub>2</sub>. The excluded volume exponents (ν ≈ 0.53-0.54) obtained from the dependence of hydrodynamic radii on molecular weight also indicate good solvent characteristics.</p>

Topics
  • impedance spectroscopy
  • polymer
  • phase
  • molecular weight
  • light scattering