Super-resolution imaging reveals resistance to mass transfer in functionalized stationary phases

ORAL

Abstract

Chemical separations are costly in terms of energy, time, and money. Separation methods are optimized with inefficient trial-and-error approaches that lack insight into the molecular dynamics that lead to the success or failure of a separation and, hence, ways to improve the process. We perform super-resolution imaging of fluorescent analytes in four different commercial liquid chromatography materials. Surprisingly, we observe that chemical functionalization can block over 50% of the material's porous interior, rendering it inaccessible to small molecule analytes. Only in situ imaging unveils the inaccessibility when compared to the industry-accepted ex situ characterization methods. Selectively removing some of the functionalization with solvent restores pore access without significantly altering the single-molecule kinetics that underlie the separation and agree with bulk chromatography measurements. Our molecular results determine that commercial “fully porous” stationary phases are over-functionalized and provide a new avenue to characterize and direct separation material design from the bottom-up.

* The Case Western Reserve University College of Arts and Sciences and RCSA Cottrell Scholar fund provided financial support for this work.

Publication: Monge Neria, R., Zeeshan, M., Kapoor, A., Gurkan, B., Duval, C. E., Saylor, R. A., Kisley, L. Super-resolution imaging reveals resistance to mass transfer in functionalized stationary phases. Submitted manuscript. October 2023.

Presenters

  • Ricardo Monge Neria

    Case Western Reserve University

Authors

  • Ricardo Monge Neria

    Case Western Reserve University

  • Lydia Kisley

    Case Western Reserve University

  • Muhammad Zeeshan

    Case Wester Reserve University

  • Aman Kapoor

    Case Western Reserve University

  • Burcu Gurkan

    Case Western Reserve University

  • Christine E Duval

    Case Western Reserve University

  • Rachel A Saylor

    Oberlin College and Conservatory