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 (7/7 displayed)

  • 2017Hole theory as a prediction tool for Brownian diffusive motion in binary mixtures of liquids13citations
  • 2017Swelling-induced structural changes and microparticle uptake of gelatin gels probed by NMR and CLSM17citations
  • 2016Adsorption of pyridine from aqueous solutions by polymeric adsorbents MN 200 and MN 500. Part 2: Kinetics and diffusion analysis99citations
  • 2015A local composition model for the prediction of mutual diffusion coefficients in binary liquid mixtures from tracer diffusion coefficients33citations
  • 2013Prediction of the mutual diffusivity in acetone-chloroform liquid mixtures from the tracer diffusion coefficients33citations
  • 2011Prediction of binary diffusion coefficients in non-ideal mixtures from NMR data: Hexane-nitrobenzene near its consolute point49citations
  • 2011Molecular motion and ion diffusion in choline chloride based deep eutectic solvents studied by H-1 pulsed field gradient NMR spectroscopy459citations

Places of action

Chart of shared publication
Gladden, Lynn F.
2 / 5 shared
Liuzzi, Roberta
1 / 1 shared
Guido, Stefano
1 / 1 shared
Moggridge, Geoff D.
2 / 3 shared
Zhu, Qingyu
2 / 2 shared
Parkinson, J. D.
1 / 1 shared
Stephens, J. A.
1 / 1 shared
Moggridge, G. D.
2 / 3 shared
Gladden, L. F.
2 / 4 shared
Mantle, M. D.
2 / 5 shared
Abbott, Andrew P.
1 / 12 shared
Harris, Robert C.
1 / 6 shared
Mantle, Mick D.
1 / 1 shared
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2011

Co-Authors (by relevance)

  • Gladden, Lynn F.
  • Liuzzi, Roberta
  • Guido, Stefano
  • Moggridge, Geoff D.
  • Zhu, Qingyu
  • Parkinson, J. D.
  • Stephens, J. A.
  • Moggridge, G. D.
  • Gladden, L. F.
  • Mantle, M. D.
  • Abbott, Andrew P.
  • Harris, Robert C.
  • Mantle, Mick D.
OrganizationsLocationPeople

article

Prediction of the mutual diffusivity in acetone-chloroform liquid mixtures from the tracer diffusion coefficients

  • Dagostino, Carmine
  • Parkinson, J. D.
  • Stephens, J. A.
  • Moggridge, G. D.
  • Gladden, L. F.
  • Mantle, M. D.
Abstract

In recent publications (D'Agostino et al., 2011; Moggridge, 2012a), we have proposed an equation to relate the mutual diffusion coefficient in a binary liquid mixture to the tracer diffusivities in the same mixture. The equation proved satisfactory for mixtures close to their consolute point as well as the general case of non-ideal mixtures; most of the available data relates to positive deviations from Raoult's law. In only one case, mixtures of acetone and chloroform, was the proposed equation not found to be consistent with the available experimental data.<br/><br/>However, the tracer diffusivity data on which this assessment was based is old (1959 and 1967), of low accuracy and with few measurements to cover the range of compositions. For this reason we have re-measured the tracer diffusivities in acetone–chloroform mixtures at 25 °C with greater accuracy, by PFG-NMR, and used these measurements to re-examine the applicability of our equation to this system.<br/><br/>We conclude that the proposed equation does in fact provide a good description of acetone–chloroform mixtures at 25 °C. This is of particular interest because acetone–chloroform shows a negative deviation from Raoult's law. The equation also gives a satisfactory fit for diethyl ether–chloroform and water-N-methylpyrrolidone (Moggridge, 2012a), both systems showing negative deviations from Raoult's law.<br/><br/>

Topics
  • impedance spectroscopy
  • diffusivity
  • Nuclear Magnetic Resonance spectroscopy
  • tracer diffusivity