Apparatus, systems and methods for in situ measurement of an oxidation / reduction potential and pH of a solution

Patent metadata

Field	Value
Publication number	US-11467124-B2
Application number	US-201816610219-A
Country	US
Kind code	B2
Filing date	May 2, 2018
Priority date	May 2, 2017
Publication date	Oct 11, 2022
Grant date	Oct 11, 2022

Abstract

Methods for in situ measurement of an oxidation reduction potential (ORP) and pH of a solution comprising iron are provided. The methods comprise measuring a kinetic parameter at an electrode surface of an electrode system comprising a working electrode, a counter electrode and a pseudo-reference electrode, wherein the kinetic parameter is associated with ferric reduction or both ferric reduction and ferrous oxidation and comparing the kinetic parameter to calibration data for the electrode system to determine the ORP and pH of the solution. Also provided are apparatus and systems for in situ measurement of an ORP and pH of a solution comprising iron. The apparatus and systems comprise an electrode system comprising a working electrode, a counter electrode and a pseudo-reference electrode and a detector for measuring a kinetic parameter at an electrode surface of the electrode system.

First claim

What is claimed is:

1. A method for in situ measurement of an oxidation/reduction potential (ORP) of a solution comprising iron, the method comprising:
measuring a kinetic parameter at an electrode surface of an electrode system comprising a working electrode, a counter electrode and a pseudo-reference electrode, wherein the kinetic parameter is associated with ferric reduction or both ferric reduction and ferrous oxidation; and
comparing the kinetic parameter to ORP calibration data for the electrode system to determine the ORP of the solution,
wherein the ORP calibration data is obtained by measuring at least two calibration solutions, each of the at least two calibration solutions comprising ferric and ferrous ions with different ratios of ferric to ferrous ions,
wherein for each of the at least two calibration solutions is measured: (a) an ORP of each calibration solution with a reference electrode, and (b) the kinetic parameter at the electrode surface of the electrode system, and
wherein the ORP of the solution corresponds to an ORP value derived from the ORP calibration data for the same kinetic parameter.

2. The method of claim 1 , wherein the kinetic parameter is current.

3. The method of claim 2 , wherein measuring the current comprises imposing a constant cathodic overpotential on the working electrode.

4. The method of claim 2 , wherein measuring the current comprises: (a) imposing an anodic overpotential followed by a cathodic overpotential on the working electrode and measuring a ratio of an anodic current to a cathodic current; or (b) imposing a cathodic overpotential followed by an anodic overpotential on the working electrode and measuring a ratio of a cathodic current to an anodic current.

5. The method of claim 1 , wherein the kinetic parameter is charge transfer resistance.

6. The method of claim 1 , wherein the reference electrode for measuring the ORP of each calibration solution is an external pressure balanced reference electrode (EPBRE) or a flow through reference electrode (FTRE).

7. The method of claim 1 , wherein the working electrode, the counter electrode and the pseudo-reference electrode each independently comprise a platinum, a gold, a carbon, a palladium or an iridium sensor.

8. The method of claim 1 , wherein the working electrode, the counter electrode and the pseudo-reference electrode each comprise a platinum wire sensor.

9. The method of claim 1 , further comprising calculating a total soluble iron concentration in the solution using the ORP of the solution.

10. The method of claim 1 , further comprising calculating an extent of sulphide oxidation in the solution using the ORP of the solution.

11. The method of claim 1 , wherein the solution is a slurry comprising iron.

12. The method of claim 1 , wherein the solution is a slurry from a pressure oxidation process.

13. The method of claim 1 , wherein the solution is at a temperature between about 25° C. and about 230° C.

14. A method for in situ measurement of a pH of a solution comprising iron, the method comprising:
measuring a kinetic parameter at an electrode surface of an electrode system comprising a working electrode, a counter electrode and a pseudo-reference electrode, wherein the kinetic parameter is associated with ferric reduction or both ferric reduction and ferrous oxidation; and
comparing the kinetic parameter to pH calibration data for the electrode system to determine the pH of the solution,
wherein the pH calibration data is obtained by measuring at least two calibration solutions, wherein each of the at least two calibration solutions comprises ferric and ferrous ions and sulphuric acid with the same ratio of ferric to ferrous ions and different sulphuric acid concentrations,
wherein for each calibration solution is measured: (a) pH, and (b) the kinetic parameter at the electrode surface of the electrode system at a potential where the kinetic parameter is dependent on a concentration of hydrogen ions in each calibration solution,
wherein the pH of the solution corresponds to a pH value derived from the pH calibration data for the same kinetic parameter.

15. The method of claim 14 , wherein the kinetic parameter is current.

16. The method of claim 15 , wherein measuring the current comprises imposing a constant cathodic overpotential on the working electrode.

17. The method of claim 15 , wherein measuring the current comprises: (a) imposing an anodic overpotential followed by a cathodic overpotential on the working electrode and measuring a ratio of an anodic current to a cathodic current; or (b) imposing a cathodic overpotential followed by an anodic overpotential on the working electrode and measuring a ratio of a cathodic current to an anodic current.

18. The method of claim 14 , wherein the reference electrode for measuring the pH of each calibration solution is an external pressure balanced reference electrode (EPBRE) or a flow through reference electrode (FTRE).

19. The method of claim 14 , wherein the working electrode, the counter electrode and the pseudo-reference electrode each independently comprise a platinum, a gold, a carbon, a palladium or an iridium sensor.

20. The method of claim 14 , wherein the working electrode, the counter electrode and the pseudo-reference electrode each comprise a platinum wire sensor.

21. The method of claim 14 , wherein the solution is a slurry comprising iron.

22. The method of claim 14 , wherein the solution is a slurry from a pressure oxidation process.

23. The method of claim 14 , wherein the solution is at a temperature between about 25° C. and about 230° C.

24. The method of claim 14 , wherein the kinetic parameter is charge transfer resistance.

Assignees

• Univ British Columbia

Inventors

• Asselin Edouard
• Zebardast Hamidreza
• Liu Jing

Classifications

• Y02P10/20

  Recycling · CPC title

• G01N27/4167

  pH (electrodes therefor G01N27/302, G01N27/36) · CPC title

• G01N27/4168 Primary

  Oxidation-reduction potential, e.g. for chlorination of water (water analysis G01N33/18) · CPC title

• G01N27/4165

  for pH meters · CPC title