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 (4/4 displayed)

  • 2024Isolation and electronic structures of lanthanide(II) bis(trimethylsilyl)phosphide complexes3citations
  • 2023Heterometallic lanthanide complexes with site-specific binding that enable simultaneous visible and NIR-emission5citations
  • 2022Hydrotalcite colloid stability and interactions with uranium(VI) at neutral to alkaline pH.16citations
  • 2018Stability, composition and core-shell particle structure of uranium(IV)-silicate colloids24citations

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Mcinnes, Eric
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Whitehead, George
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Baldwin, Jack
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Oakley, Meagan
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Brookfield, Adam
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Mills, David
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Parkinson, Patrick
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Hay, Sam
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Thornton, Matthew
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Faulkner, Stephen
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Hemsworth, Jake
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Haigh, Sj
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Harrison, Robert W.
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Neill, Thomas
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Sherriff, Nick
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Wilson, Hannah
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Shaw, Samuel
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Bryan, Nick
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Morris, Katherine
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Zou, Yi Chao
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Sherriff, Nicholas K.
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Pearce, Carolyn
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Janssen, Arne
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Neill, Thomas Samuel
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Chater, Philip
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Co-Authors (by relevance)

  • Mcinnes, Eric
  • Whitehead, George
  • Baldwin, Jack
  • Oakley, Meagan
  • Brookfield, Adam
  • Mills, David
  • Parkinson, Patrick
  • Hay, Sam
  • Thornton, Matthew
  • Faulkner, Stephen
  • Hemsworth, Jake
  • Haigh, Sj
  • Harrison, Robert W.
  • Neill, Thomas
  • Sherriff, Nick
  • Wilson, Hannah
  • Odriozola, Laura Lopez
  • Shaw, Samuel
  • Foster, Chris
  • Bryan, Nick
  • Morris, Katherine
  • Rigby, Bruce
  • Zou, Yi Chao
  • Sherriff, Nicholas K.
  • Pearce, Carolyn
  • Janssen, Arne
  • Neill, Thomas Samuel
  • Chater, Philip
OrganizationsLocationPeople

article

Hydrotalcite colloid stability and interactions with uranium(VI) at neutral to alkaline pH.

  • Haigh, Sj
  • Harrison, Robert W.
  • Neill, Thomas
  • Sherriff, Nick
  • Wilson, Hannah
  • Odriozola, Laura Lopez
  • Shaw, Samuel
  • Natrajan, Louise
  • Foster, Chris
  • Bryan, Nick
  • Morris, Katherine
  • Rigby, Bruce
  • Zou, Yi Chao
Abstract

In the UK, decommissioning of legacy spent fuel storage facilities involves the retrieval of radioactive sludges that have formed as a result of corrosion of Magnox nuclear fuel. Retrieval of sludges may re-suspend a colloidal fraction of the sludge, thereby potentially enhancing the mobility of radionuclides including uranium. The colloidal properties of the layered double hydroxide (LDH) phase hydrotalcite, a key product of Magnox fuel corrosion, and it’s interactions with U(VI) are of interest. This is because colloidal hydrotalcite is a potential transport vector for U(VI) under the neutral-to-alkaline conditions characteristic of the legacy storage facilities and other nuclear decommissioning scenarios. Here, a multi-technique approach was used to investigate the colloidal stability of hydrotalcite and the U(VI) sorption mechanism(s) across pH 7 – 11.5 and with variable U(VI) surface loadings (0.01 – 1 wt%). Overall, hydrotalcite was found to form stable colloidal suspensions between pH 7 and 11.5, with some evidence for Mg2+ leaching from hydrotalcite colloids at pH ≤ 9. For systems with U present, >98% of U(VI) was removed from solution in the presence of hydrotalcite, regardless of pH and U loading, although the sorption mode was affected by both pH and U concentration. Under alkaline conditions, U(VI) surface precipitates formed on the colloidal hydrotalcite nanoparticle surface. Under more circumneutral conditions, Mg2+ leaching from hydrotalcite and more facile exchange of interlayer carbonate with the surrounding solution led to the formation of uranyl carbonate species (e.g. Mg[UO2(CO3)3]2-(aq)). Both X-ray absorption spectroscopy (XAS) and luminescence analysis confirmed these negatively charged species sorbed as both outer- and inner-sphere tertiary complexes on the hydrotalcite surface. These results demonstrate that hydrotalcite can form pseudo-colloids with U(VI) under a wide range of pH conditions and have clear implications for understanding uranium behaviour in environments where hydrotalcite and other LDHs may be present.

Topics
  • nanoparticle
  • impedance spectroscopy
  • surface
  • corrosion
  • phase
  • mobility
  • layered
  • precipitate
  • leaching
  • x-ray absorption spectroscopy
  • Uranium
  • luminescence