Electrochemical pH measurement

• US 9,244,034 B2
• Filed: 05/04/2012
• Issued: 01/26/2016
• Est. Priority Date: 11/04/2010
• Status: Active Grant

• Current Assignee: Schlumberger Technology Corporation (Schlumberger NV)
• Original Assignee: Schlumberger Technology Corporation (Schlumberger NV)
• Inventors: Lawrence, Nathan S., Meredith, Andrew
• Primary Examiner(s): NOGUEROLA, ALEXANDER STEPHAN
• Application Number:
  US13/464,700
• Publication Number:
  US 20120279874A1
• Time in Patent Office: 1,362 Days
• US Class Current: 1/1
• CPC Class Codes: G01N 27/30 Electrodes, e.g. test electrodes; Half-cells G01N27/414 takes precedence
• CPC Class Codes: G01N 27/302 pH sensitive, e.g. quinhydron, antimony or hydrogen electrodes ion selective electrodes G01N27/333, glass electrodes G01N27/36
• CPC Class Codes: G01N 27/4167 pH electrodes therefor G01N27/302, G01N27/36

Abstract

A method of measuring pH of aqueous liquid with little or no buffer present uses an electrochemical pH sensor which comprises a plurality of electrodes with a redox active organic compound attached to an electrode and having at least one functional group convertible electrochemically between reduced and oxidized forms with transfer of at least one proton between the compound and surrounding aqueous phase, wherein the compound has at least one substituent group which promotes hydrogen bonding at a said functional group and thereby increases the reaction rate of proton transfer. The substituent group may form an internal hydrogen bond with a redox-convertible group or may enhance polarity to promote electrostatic interaction with water molecules and reduce activation energy. Such an electrochemical sensor may be used for pH measurement in computer controlled equipment for processing an aqueous liquid.

Claims

1. A method of measuring the pH of an aqueous liquid, comprising

exposing the aqueous liquid comprising buffer at a concentration of 0.01 molar or less to an electrochemical sensor comprising an electrode with a redox active compound immobilized to the electrode with at least one functional group convertible electrochemically between reduced and oxidized forms upon transfer of at least one proton between the compound and surrounding aqueous phase,

wherein the reduced form of the redox active compound incorporates a partial structure,

2. A method according to claim 1 comprising applying variable potential to the electrode with the redox-active compound immobilized thereon;

and determining the applied potential at a maximum current for redox reaction of the compound.

3. A method according to claim 1 wherein the aqueous liquid is unbuffered water.

4. A method according to claim 1 wherein the aqueous liquid contains buffer at a concentration of at least 10⁻

6 molar.

5. A method according to claim 1 wherein the carbon atoms of the redox active organic compound, which are joined by conjugated bonds, are provided by at least two fused aromatic rings.

6. A method according to claim 5 wherein said compound comprises at least two fused aromatic rings, which has two keto substituents on a first aromatic ring and two oxygen-containing functional group convertible between hydroxyl and keto forms on a second aromatic ring fused with the first said ring.

7. A method according to claim 5, wherein the compound comprises at least two fused aromatic rings with two keto substituents on a first aromatic ring and at least two nitrogen containing functional groups, convertible between reduced and oxidized forms, on a second aromatic ring fused with the first said ring, and the compound further having electron withdrawing substituents reducing the basicity of the nitrogen-containing functional group.

8. A method according to claim 5 wherein said redox active organic compound further comprises an electron withdrawing group.

9. A method according to claim 1, wherein the redox active compound is selected from 1,4-diamino-2,3-dihalo-naphthoquinone, 2-acetylbenzoquinone, 2,3-diacetylbenzoquinone, 1,2-dihydroxynaphthoquinone, 1,4-dihydroxynaphthoquinone and homologues and analogues of these compounds which have additional substituents or have additional rings fused with the benzoquinone or naphthoquinone rings, and wherein the keto groups of the benzoquinone or napthoquinone may be in ortho or para positions relative to each other.

10. A sensor according to claim 1 comprising a plurality of electrodes with the redox active compound immobilized on one of the electrodes.

11. A method according to claim 1 wherein the sensor further comprises a second redox active compound as a reference, immobilized to the same or another electrode, the oxidation and reduction of the second redox active compound being substantially insensitive to pH.