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)

  • 2004Effect of Composition on the Width of the Calorimetric Glass Transition in Polymer-Solvent and Solvent-Solvent Mixtures66citations

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Savin, Daniel A.
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2004

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  • Savin, Daniel A.
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article

Effect of Composition on the Width of the Calorimetric Glass Transition in Polymer-Solvent and Solvent-Solvent Mixtures

  • Savin, Daniel A.
  • Larson, Anne M.
Abstract

<p>The calorimetric glass-transition temperature (T<sub>g</sub>) and transition width were measured over the full composition range for solvent-solvent mixtures of o-terphenyl with tricresyl phosphate and with dibutyl phthalate and for polymer-solvent mixtures of polystyrene with three dialkyl phthalates. T<sub>g</sub> shifted smoothly to higher temperatures with the addition of the component with the higher T<sub>g</sub> for both sets of solvent-solvent mixtures. The superposition of the differential scanning calorimetry traces showed almost no composition dependence for the width of the transition region. In contrast, the composition dependence of T<sub>g</sub> in polymer-solvent mixtures was different at high and low polymer concentrations, and two distinct T<sub>g</sub>'s were observed at intermediate compositions. These results were interpreted in terms of the local length scale and associated local composition variations affecting T<sub>g</sub>. The possible implications of these results for the dynamics of miscible polymer blends were examined.</p>

Topics
  • glass
  • glass
  • differential scanning calorimetry
  • polymer blend