Voltammetric method of measuring

• US 4,786,373 A
• Filed: 05/13/1987
• Issued: 11/22/1988
• Est. Priority Date: 12/29/1983
• Status: Expired due to Fees

• Current Assignee: Outokumpu Oyj
• Original Assignee: Outokumpu Oyj
• Inventors: Saloheimo, Kari M. O., Rantapuska, Seppo V.
• Primary Examiner(s): Niebling, John F.
• Assistant Examiner(s): Nguyen, Nam X.
• Application Number:
  US07/050,056
• Time in Patent Office: 559 Days
• Field of Search: 204/1 T, 204/400, 204/402, 204/409, 204/DIG. 9, 204/434, 73/861.12
• US Class Current: 205/789.5
• CPC Class Codes: G01N 2291/02809 Concentration of a compound, e.g. measured by a surface mass change
• CPC Class Codes: G01N 27/42 Measuring deposition or liberation of materials from an electrolyte; Coulometry, i.e. measuring coulomb-equivalent of material in an electrolyte

Abstract

A stripping analysis method comprises a preelectrolysis step during which liquid to be analyzed is introduced into a measurement cell at a pulsating rate, a working electrode is vibrated at an ultrasonic frequency, and the voltage potential between the working electrode and a reference electrode is adjusted to a level which allows the substances to be determined to be deposited on the working electrode. After the preelectrolysis step is a stripping step during which the voltage potential between the working electrode and the reference electrode is scanned through the potential range where the substances to be determined are dissolved back to the liquid and current is measured while the liquid in the measurement cell remains essentially undisturbed. The method also comprises an elimination step during which the voltage potential between the working electrode and the reference electrode is adjusted to a level at which the working electrode is regenerated. The products of the measurement step are removed from the cell by vibrating the working electrode at an ultrasonic frequency and thereby disturbing the liquid in the cell, and introducing liquid into the cell at a non-pulsating rate and thereby displacing liquid from the cell.

Claims

1. A stripping analysis method for analyzing a liquid using a measurement device that comprises wall means defining a measurement cell for receiving liquid to be analyzed, and also comprises a solid working electrode and a reference electrode tat contact liquid in the cell, said method comprising the following steps, in the order stated:

(a) a preelectrolysis step during which liquid to be analyzed is introduced into the measurement cell at a pulsating rate, the working electrode is vibrated at an ultrasonic frequency, and the voltage potential between the working electrode and the reference electrode is adjusted to a level which allows the substances to be determined to be deposited on the working electrode,

(b) a stripping step during which the voltage potential between the working electrode and the reference electrode is scanned through the potential range where the substances to be determined are dissolved back to the liquid and current is measured while the liquid in the measurement cell remains essentially undisturbed, and

(c) an elimination step during which the voltage potential between the working electrode and the reference electrode is adjusted to a level at which the working electrode is regenerated and the products of the measurement step are removed from the cell by vibrating the working electrode at an ultrasonic frequency and thereby disturbing the liquid in the cell, and introducing liquid into the cell at a non-pulsating rate and thereby displacing liquid from the cell.

2. An improved stripping analysis method for analyzing a liquid using a measurement device that comprises wall means defining a measurement cell for receiving a liquid to be analyzed, and also comprises a solid working electrode and a reference electrode that contact liquid in the cell, said method comprising the following steps, in the order stated:

(a) a pre-electrolysis step during which liquid to be analyzed is introduced into the measurement cell and the voltage potential between the working electrode and the reference electrode is adjusted to a level which allows the substances to be determined to be deposited on the working electrode,

(b) a stripping step during which the voltage potential between the working electrode and the reference electrode is scanned through the potential range where the substances to be determined are dissolved back to the liquid and current is measured while the liquid in the measurement cell remains essentially undisturbed, and

(c) an elimination step during which the voltage potential between the working electrode and the reference electrode is adjusted to a level at which the working electrode is regenerated and the products of the measurement step are removed from the cell,

and wherein the improvement resides in that during the pre-electrolysis step the liquid to be analyzed is introduced into the measurement cell at a pulsating rate and the working electrode is vibrated at an ultrasonic frequency.

3. A method according to claim 2, wherein during the elimination step the products of the measurement step are removed from the cell by vibrating the working electrode at an ultrasonic frequency and thereby disturbing the liquid in the cell, and introducing liquid into the cell at a non-pulsating rate and thereby displacing liquid from the cell.