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Preparation of surface-coated macroporous silica (core-shell silica monolith) for HPLC separations

Graphical Abstract
  • Risako Ito
  • Kei Morisato
  • Kazuyoshi Kanamori
  • Kazuki Nakanishi
Original Paper: Nano- and macroporous materials (aerogels, xerogels, cryogels, etc.)
  • 48 Downloads

Abstract

Utilizing the spontaneous wetting of oligomeric silica-phase via phase-separation onto a solid surface in a confined dimension, sub-micrometer thick mesoporous layers have been coated on the surface of nonporous skeletons of preformed macroporous silica gels. The size and volume of mesopores within the layers could be controlled by subsequent aging conditions similarly to those reported for fully porous monolithic silica. Comparison of HPLC efficiencies of these novel type monolithic gels, core-shell silica monoliths, with those of a conventional silica monolith revealed that the retention factor per unit surface area became larger for core-shell silica monoliths. The increase in dynamic accessibility of analyte molecules to the mesopores well explain the improved retention factors in core-shell silica monoliths.

Core-shell monoliths with mesoporous layers coated on the surface of micrometer-sized fully-sintered continuous silica skeletons for HPLC separations.

Highlights

  • Macroporous silica monolith with fully sintered skeletons has been used as a host for core-shell silica monolith.

  • Onto the surface of the skeletons, oligomeric silica has been coated utilizing the wetting transition associated with the phase separation in a confined space.

  • Monolithic silica with well-defined continuous macropores and superficially mesoporous silica skeletons was proven to work as an efficient HPLC separation medium.

Keywords

Silica Macroporous monoliths Phase separation Wetting transition Separation medium HPLC 

Notes

Acknowledgements

Financial support by KAKENHI(18H02056) JSPS, Japan is gratefully acknowledged.

Compliance with ethical standards

Conflict of interest

The authors declare that they have no conflict of interest.

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Copyright information

© Springer Science+Business Media, LLC, part of Springer Nature 2018

Authors and Affiliations

  1. 1.Department of Chemistry, Graduate School of ScienceKyoto University, KitashirakawaSakyo-kuJapan

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