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
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Hubin, Annick
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Schmidt, Philipp
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Collet, Thomas
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Baron, Gino
2 / 12 shared
Terryn, Herman
1 / 124 shared
Wirth, Mary J.
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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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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

document

High-pressure ion chromatography in capillary columns and microfluidic chips

  • Wouters, Bert
  • Eeltink, Sebastiaan
  • Eghbali, Hamed
Abstract

Similar like in high-performance liquid chromatography, ion chromatography (IC) has witnessed a trend toward the use of smaller particle packing materials to increase the separation performance. Without compromising the column length, the use of smaller particles leads to higher operating pressure, since the pressure drop is inversely proportional to the square of the particle diameter. To withstand the higher operating pressures and to improve the solvent compatibility the crosslink density of the polymer beads has been increased from 5% to > 50% for today's particles. To meet the demand for analyzing minute amounts of sample there is also strong interest in miniaturization of column technology. Additional benefits of using smaller column I.D.'s are the increased detection sensitivity, and better compatibility with electrospray-ionization mass spectrometry (especially when using aqueous mobile-phases). This has now resulted in the development of capillary IC columns formats and high-pressure capillary systems that are compatible with alkaline mobile-phase. The present contribution discusses the IC performance limits that can be achieved with capillary columns packed with 4 and 7 µm polymer anion-exchange beads, respectively. When operating in the C-term region of the Van Deemter curve a 26% increase in efficiency and maximum time gain of 45% could be established employing 4 µm packed columns and increasing the operating pressure from 3000 to 5000 psi. In addition, the effects of column temperatures up to 80°C on kinetic performance limits and selectivity are discussed for mono-, di-, and trivalent anions.Finally, a the design of a prototype microfluidic chip for IC will be discussed. Different channel layouts were created using a precision micro-milling robot instrument allowing the engineering of channel diameters of 100 µm I.D. and larger. The possibilities to packed chips with polymer IC bead and the in-situ polymerization of monolithic stationary phases are discussed.

Topics
  • density
  • impedance spectroscopy
  • polymer
  • phase
  • grinding
  • milling
  • mass spectrometry
  • spectrometry
  • High-performance liquid chromatography
  • ion chromatography
  • in-situ polymerization