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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Materials Map under construction

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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Bartenstein, Julia E.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (4/4 displayed)

  • 2016Influence of solvent polarity on the structure of drop-cast electroactive tetra(aniline)-surfactant thin films22citations
  • 2016Influence of solvent polarity on the structure of drop-cast electroactive tetra(aniline)-surfactant thin films22citations
  • 2016Hydrophilic nanoparticles stabilising mesophase curvature at low concentration but disrupting mesophase order at higher concentrations14citations
  • 2016Stability of polymersomes prepared by size exclusion chromatography and extrusion47citations

Places of action

Chart of shared publication
Faul, Charl F. J.
2 / 12 shared
Macdonald, J. Emyr
1 / 5 shared
Mills, Benjamin
1 / 1 shared
Bell, O. Alexander
2 / 2 shared
Dane, Thomas G.
2 / 2 shared
Sironi, Beatrice
2 / 4 shared
Arnold, Thomas
2 / 14 shared
Briscoe, Wuge H.
4 / 27 shared
Emyr Macdonald, J.
1 / 1 shared
Mills, Benjamin M.
1 / 1 shared
Berge, Johanna
1 / 1 shared
Heenan, Richard K.
1 / 12 shared
Lange, Kathrin
1 / 2 shared
Beddoes, Charlotte M.
1 / 1 shared
Smith, Andrew J.
1 / 8 shared
Battaglia, Giuseppe
1 / 2 shared
Robertson, James
1 / 2 shared
Chart of publication period
2016

Co-Authors (by relevance)

  • Faul, Charl F. J.
  • Macdonald, J. Emyr
  • Mills, Benjamin
  • Bell, O. Alexander
  • Dane, Thomas G.
  • Sironi, Beatrice
  • Arnold, Thomas
  • Briscoe, Wuge H.
  • Emyr Macdonald, J.
  • Mills, Benjamin M.
  • Berge, Johanna
  • Heenan, Richard K.
  • Lange, Kathrin
  • Beddoes, Charlotte M.
  • Smith, Andrew J.
  • Battaglia, Giuseppe
  • Robertson, James
OrganizationsLocationPeople

article

Hydrophilic nanoparticles stabilising mesophase curvature at low concentration but disrupting mesophase order at higher concentrations

  • Bartenstein, Julia E.
  • Berge, Johanna
  • Heenan, Richard K.
  • Lange, Kathrin
  • Briscoe, Wuge H.
  • Beddoes, Charlotte M.
  • Smith, Andrew J.
Abstract

Using high pressure small angle X-ray scattering (HP-SAXS), we have studied monoolein (MO) mesophases at 18 wt% hydration in the presence of 10 nm silica nanoparticles (NPs) at NP-lipid number ratios (ν) of 1 × 10 -6 , 1 × 10 -5 and 1 × 10 -4 over the pressure range 1-2700 bar and temperature range 20-60 °C. In the absence of the silica NPs, the pressure-temperature (p-T) phase diagram of monoolein exhibited inverse bicontinuous cubic gyroid (QGII), lamellar alpha (L α ), and lamellar crystalline (L c ) phases. The addition of the NPs significantly altered the p-T phase diagram, changing the pressure (p) and the temperature (T) at which the transitions between these mesophases occurred. In particular, a strong NP concentration effect on the mesophase behaviour was observed. At low NP concentration, the p-T region pervaded by the QGII phase and the L α -QGII mixture increased, and we attribute this behaviour to the NPs forming clusters at the mesophase domain boundaries, encouraging transition to the mesophase with a higher curvature. At high NP concentrations, the QGII phase was no longer observed in the p-T phase diagram. Instead, it was dominated by the lamellar (L) phases until the transition to a fluid isotropic (FI) phase at 60 °C at low pressure. We speculate that NPs formed aggregates with a "chain of pearls" structure at the mesophase domain boundaries, hindering transitions to the mesophases with higher curvatures. These observations were supported by small angle neutron scattering (SANS) and scanning electron microscopy (SEM). Our results have implications to nanocomposite materials and nanoparticle cellular entry where the interactions between NPs and organised lipid structures are an important consideration.

Topics
  • nanoparticle
  • nanocomposite
  • cluster
  • phase
  • scanning electron microscopy
  • forming
  • isotropic
  • phase diagram
  • small-angle neutron scattering
  • small angle x-ray scattering
  • gyroid