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Fast‐pulsed electrochemical detection at noble metal electrodes: The frequency‐dependent response at gold electrodes for chromatographically separated carbohydrates
Author(s) -
Roberts Richard E.,
Johnson Dennis C.
Publication year - 1994
Publication title -
electroanalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.574
H-Index - 128
eISSN - 1521-4109
pISSN - 1040-0397
DOI - 10.1002/elan.1140060402
Subject(s) - waveform , electrode , elution , electrochemistry , detector , signal (programming language) , capillary electrophoresis , analytical chemistry (journal) , chemistry , anode , materials science , chromatography , noble metal , metal , optics , voltage , computer science , electrical engineering , physics , programming language , organic chemistry , engineering
Waveforms used in pulsed electrochemical detection (PED) have frequencies of ca. 1 Hz when optimized to give a maximum signal‐to‐noise ratio ( S / N ) for carbohydrates. However, higher frequencies are desired for application of PED to capillary electrophoresis (CE) and microcolumn lipuid chromatography (MLC), which can produce narrow elution peaks. Minimization of the time periods for oxidative cleaning and reductive reactivation in PED waveforms generated by the Dionex pulsed Electrochemical Detector allows the increase in waveform frequency to ca. 3 Hz without change in the traditional time period of 200 ms, prescribed for integration of the anodic current. However, further increase in frequency requires a decrease in the integration period with a corresponding loss of signal strength.