Abstract
A hydrodynamic system based on the channel flow cell for voltammetric detection of ions at the liquid/liquid interface is reported. The current response for tetraethylammonium ion transfer across a membrane-supported liquid/liquid interface is shown to be consistent with existing theory for both the flow rate and voltage scan rate dependence of such processes, with no calibration factors or other adjustable parameters required. The analytical utility of such a device is discussed with specific regard to in situ measurements in flow systems.
Original language | English |
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Pages (from-to) | 486-493 |
Number of pages | 7 |
Journal | Analytical Chemistry |
Volume | 75 |
Issue number | 3 |
DOIs | |
Publication status | Published - 1 Feb 2003 |