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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Eeltink, Sebastiaan

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Vrije Universiteit Brussel

in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (6/6 displayed)

  • 2022An ex situ and operando analysis of thiourea consumption and activity during a simulated copper electrorefining process3citations
  • 2020Evaluation of particle and bed integrity of aqueous size-exclusion columns packed with sub-2 µm particles operated at high pressure4citations
  • 2015Poster: A comprehensive study of the macro- and mesopores size distributions of polymer monoliths using complementary physical characterization techniquescitations
  • 2012High-pressure ion chromatography in capillary columns and microfluidic chipscitations
  • 2011High-resolution separations of protein isoforms with liquid chromatography time-of-flight mass spectrometry using polymer monolithic capillary columnscitations
  • 2011Ultra-high-resolution separations of intact proteins with LC-TOF-MS using polymer monolithic columnscitations

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Ramharter, Kristof
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Wouters, Benny
1 / 13 shared
Hubin, Annick
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Schmidt, Philipp
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Collet, Thomas
1 / 7 shared
Baron, Gino
2 / 12 shared
Terryn, Herman
1 / 124 shared
Wirth, Mary J.
1 / 1 shared
Vos, Jelle De
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Kaal, Erwin
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Wouters, Sam
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Wouters, Bert
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Eghbali, Hamed
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Desmet, Gert
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Treumann, A.
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Ursem, Mario
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Blinco, D.
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Kemp, G. D.
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Treumann, Achim
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2020
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Co-Authors (by relevance)

  • Ramharter, Kristof
  • Wouters, Benny
  • Hubin, Annick
  • Schmidt, Philipp
  • Collet, Thomas
  • Baron, Gino
  • Terryn, Herman
  • Wirth, Mary J.
  • Vos, Jelle De
  • Kaal, Erwin
  • Wouters, Sam
  • Wouters, Bert
  • Eghbali, Hamed
  • Desmet, Gert
  • Treumann, A.
  • Ursem, Mario
  • Blinco, D.
  • Kemp, G. D.
  • Treumann, Achim
OrganizationsLocationPeople

article

Evaluation of particle and bed integrity of aqueous size-exclusion columns packed with sub-2 µm particles operated at high pressure

  • Eeltink, Sebastiaan
  • Baron, Gino
  • Terryn, Herman
  • Wirth, Mary J.
  • Vos, Jelle De
  • Kaal, Erwin
Abstract

<p>The performance of columns packed with 1.7 µm particles for aqueous size-exclusion chromatography was assessed at high-pressure conditions and linked to particle- and column-bed integrity. Decreasing the particle size from 3.5 µm to 1.7 µm increases the resolution due to the improved mass-transfer characteristics, allowing to significantly speed-up analysis without compromising the selectivity. A sub-minute separation of intact proteins was realized on a 4.6 mm i.d × 75 mm long column packed with 1.7 µm SEC particles applying a flow rate of 1.8 mL/min, corresponding to a column pressure of 530 bar. Ultra-high pressure operation (exceeding manufacturer's recommendations) resulted in peak deformation, a shift towards earlier retention times, and an alteration in selectivity. To gain insights in the mechanisms of column deterioration, short 30 mm long columns were operated at UHPLC conditions, maximizing the pressure drop over individual particles. This resulted in the presence of fractured particles situated at the column outlet, as verified by scanning electron micrographs. Mercury-intrusion porosimetry and argon-adsorption measurements did not reveal significant differences in intraparticle volume between particle batches sampled before and after pressure stress testing. As particles at the column outlet fracture (but not collapse) at high pressure operation, a void was formed at the column inlet. The degradation of the separation performance appeared to be the result of a decrease in interparticle pore volume.</p>

Topics
  • pore
  • void
  • size-exclusion chromatography
  • porosimetry
  • Mercury