Issue 11, 2021

Sample preparation under turbulent flow with renewable sorbent

Abstract

Turbulent flow chromatography is an online solid phase extraction mode that achieves the extraordinary effect of proxying an upper molecular weight cutoff for the retained molecules, based on loading the sample at high linear velocities. Despite the potential of being a universal sample preparation technique prior to inductively coupled plasma mass spectrometry and liquid chromatography mass spectrometry, it employs specific hardware and expensive consumables. In the present work we apply this technique using off-the-shelf fluidic components and the niche “bead injection” methodology. For the first time, this procedure has been executed with a pressure of approximately 20 bar, compared to the low pressure of the classic setup, achieving a sample throughput >285 h−1 for the SPE/TFC procedure, or 20 h−1 if the procedure involves renewing the sorbent, using no more than 4 mg of sorbent for every μ-SPE. Another novelty is that sorbent packing and unpacking has been controlled with a smart method using real-time pressure feedback as quality control for truly unattended operation. Finally, the turbulent flow chromatography principle has been comprehensively characterized, providing similar performance to that demonstrated in earlier literature, and the ancillary sample preparation capabilities, e.g., in-valve acidification, have been demonstrated by the fractionation of gadolinium in surface waters prior to ICP-MS, an element of increasing surface water concern due to its use as a magnetic resonance contrast agent.

Graphical abstract: Sample preparation under turbulent flow with renewable sorbent

Supplementary files

Article information

Article type
Communication
Submitted
20 Jul 2021
Accepted
07 Sep 2021
First published
07 Oct 2021
This article is Open Access
Creative Commons BY license

J. Anal. At. Spectrom., 2021,36, 2306-2311

Sample preparation under turbulent flow with renewable sorbent

D. J. Cocovi-Solberg, S. Schnidrig and S. Hann, J. Anal. At. Spectrom., 2021, 36, 2306 DOI: 10.1039/D1JA00252J

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