Multiparameter analytical electrode structure and method of measurement

• US 4,798,655 A
• Filed: 03/19/1987
• Issued: 01/17/1989
• Est. Priority Date: 03/19/1987
• Status: Expired due to Term

• Current Assignee: Diamond General Development Corporation
• Original Assignee: Diamond General Development Corporation
• Inventors: Diamond, Howard
• Primary Examiner(s): Niebling, John F.
• Assistant Examiner(s): Hsing, Ben C.
• Application Number:
  US07/027,846
• Time in Patent Office: 670 Days
• Field of Search: 204/1 T, 204/1 Y, 204/1 K, 204/1 F, 204/1 H, 204/416, 204/431, 204/432, 204/433, 204/435
• US Class Current: 205/775
• CPC Class Codes: A61C 19/04 Measuring instruments specially adapted for dentistry A61C5/44 takes precedence; testing vitality of teeth A61B5/0534; radiation diagnosis specially adapted for dentistry A61B6/51
• CPC Class Codes: G01N 27/4035 Combination of a single ion-sensing electrode and a single reference electrode G01N27/406 and G01N27/413 take precedence

Abstract

An ion sensitive electrode device and method of its use in analytical and clinical chemistry are provided for measuring the concentration of an ionizable analyte contained in an aqueous medium. The device with external circuit means includes an electrode pair adapted to be placed in electrochemical contact with the medium. The electrode pair includes a polarographically active base metal/metal oxide working electrode and a reference electrode. The external circuit means is adapted to measure the voltage generated by the electrode pair in open circuit and to measure the closed circuit current flow at a preselected impedance and including means for comparing said voltage and current flow values with predetermined reference standards to provide a third value representative of said analyte concentration.

Claims

1. The electrochemical method of simultaneously or sequentially measuring in a liquid both a dissolved ionic species and a dissolved gas including the steps of:

(a) providing a single polarographically active working electrode having an electrochemically active, base metal/metal oxide surface having the property of providing a stable electrochemical potential that is a quantitative measure of said ionic species and acting as a catalyst for electron transfer allowing for a quantitative polarographic or amperometric measure of said dissolved gas;

(b) providing a reference electrode;

(c) measuring the open circuit voltage generated by the electrode pair;

(d) measuring the closed circuit current flow either in driven mode or in self-generated mode, and comparing said voltage and current values with predetermined voltage and current reference standards to provide multiple values of parameters representative of concentrations of said ionic species and dissolved gas.

2. The method according to claim 1 where the working electrode is a self-renewing base metal electrode.

3. The method according to claim 1 where the working electrode is an antimony/antimony oxide electrode.

4. The method according to claim 2 where the reference electrode is a silver/silver chloride electrode or calomel electrode.

5. The method according to claim 1 where the current flow measured is that of the short circuit current flow.

6. The method according to claim 1 where the concentration of dissolved oxygen is measured.

7. The method according to claim 1 where the concentration of dissolved hydrogen is measured.

8. The method according to claim 1 where the concentration of dissolved hydrogen sulfide is measured.

9. The method according to claim 1 where the hydrogen ion concentration is measured.

10. The electrochemical method of measuring the concentration of an ionizable analyte and two dissolved gaseous analytes contained in an aqueous solution, comprising the steps of:

(a) providing a base metal/metal oxide working electrode which is polarographically active in the presence of the gaseous analytes;

(b) providing a reference electrode;

(c) carrying out first and second measurements of the polarographic current at given first and second applied steady-state voltages, respectively, and comparing the resulting observed first and second current values with predetermined reference standards to provide two values representative of the concentrations of two gas analytes of interest; and

,

(d) measuring the open circuit voltage, said voltage correlatable with the concentration of the ionizable analyte.

11. The method according to claim 10 where the working electrode is a self-renewing base metal electrode.

12. The method according to claim 10 where the working electrode is an antimony/antimony oxide electrode.

13. The method according to claim 11 where the reference electrode is a silver/silver chloride electrode or calomel electrode.

14. The method according to claim 10 where the concentration of oxygen is measured.

15. The method according to claim 10 where the concentration of dissolved hydrogen is measured.

16. The method according to claim 10 where the concentration of hydrogen sulfide is measured.