USGS Science⌕ Search

Geology topics

J. H. Christie

Publications and source records attributed to J. H. Christie.

5 recordsLinked to original sources

Square wave voltammetry at the dropping mercury electrode: Theory

The theoretical aspects of square wave voltammetry at the dropping mercury electrode are presented. The technique involves scanning the entire potential range of interest on a single drop of a DME. Asymmetries in the waveform as well as variations in current measurement parameters are discussed. Indications are that previous uses of the waveform may not have utilized all its capabilities.

Analytical Chemistry↗

Square wave voltammetry at the dropping mercury electrode: Experimental

Experimental verification of earlier theoretical work for square wave voltammetry at the dropping mercury electrode is given. Experiments using ferric oxalate and cadmium(II) in HCl confirm excellent agreement with theory. Experimental peak heights and peak widths are found to be within 2% of calculated results. An example of trace analysis using square wave voltammetry at the DME is presented. The technique is shown to have the same order of sensitivity as differential pulse polarography but is much faster to perform. A detection limit for cadmium in 0.1 M HCl for the system used here was 7 ?? 10-8 M.

Analytical Chemistry↗

Alternate drop pulse polarography

The new technique of alternate drop pulse polarography is presented. An experimental evaluation of alternate drop pulse polarography shows complete compensation of the capacitative background due to drop expansion. The capillary response phenomenon was studied in the absence of faradaic reaction and the capillary response current was found to depend on the pulse width to the -0.72 power. Increased signal-to-noise ratios were obtained using alternate drop pulse polarography at shorter drop times.

Analytical Chemistry↗

Constant potential pulse polarography

The new technique of constant potential pulse polarography, In which all pulses are to be the same potential, is presented theoretically and evaluated experimentally. The response obtained is in the form of a faradaic current wave superimposed on a constant capacitative component. Results obtained with a computer-controlled system exhibit a capillary response current similar to that observed In normal pulse polarography. Calibration curves for Pb obtained using a modified commercial pulse polarographic instrument are in good accord with theoretical predictions.

Analytical Chemistry↗