Abstract
The mass transport properties of a non-retained (thiourea) and three retained low molecular weight compounds (acetophenone, valerophenone, and octanophenone) along a 4.6mm×45mm PROSWIFT™ RP-1S monolithic column made of rigid cross-linked poly(styrene-divinylbenzene) copolymer was investigated in depth. Accurate protocols (peak parking experiments, measurement of the first and second central moments of peak profiles by numerical integration) combined with the use of validated models of effective diffusion along monolithic structures were applied for the determination of the longitudinal diffusion, the eddy dispersion, and the skeleton–eluent mass transfer resistances due to the finite analyte diffusivity across the polymer skeleton and to the slow absorption kinetics into the polymer volume. Experimental results show by increasing order of importance evidence that the resolution performance of this short and wide polymer-based monolithic HPLC column is limited by the slow analyte diffusivity across the polymer skeleton (smaller than one tenth of the bulk diffusion coefficient for k′>1), its large eddy dispersion HETP (Heddy≃100μm), and the slow rate of absorption (≃10Hz only) in the polymer volume for retained analytes. The column performance could be improved by preparing a more homogeneous material with a rigid internal mesoporous structure. This would provide a column bed having a larger specific surface area, allowing faster analyte diffusion across the mesoporous skeleton, a smaller eddy dispersion HETP, and a faster absorption kinetics in the polymeric monolith than those observed for the currently available materials.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.