Electrochemical Method and Device for Measuring the Different Uncomplexed Forms of Sulphur Dioxide in an Aqueous Liquid Medium

Patent metadata

Field	Value
Publication number	US-2019376930-A1
Application number	US-201816487174-A
Country	US
Kind code	A1
Filing date	Feb 20, 2018
Priority date	Feb 21, 2017
Publication date	Dec 12, 2019
Grant date	—

Abstract

The invention relates to an electrochemical method and device for detecting and/or quantifying sulphur dioxide (S(¾) in its various uncomplexed forms (molecular and ionic) in an aqueous or hydroalcoholic liquid food product. It also relates to a method for regenerating an electrode, the active surface of which is composed of gold. The electrochemical method for detecting and/or quantifying sulphur dioxide (SO2) in its uncomplexed (free) forms in an aqueous or hydroalcoholic liquid food product of the invention comprises: a) introducing into the liquid food product a measuring electrode, the active surface of which, in contact with the liquid food product is entirely made of gold, b) measuring the variation of the current produced by the oxidisation of the free SC½, present in the food liquid, during a potential sweep by cyclic voltammetry. In particular, the invention is used for measuring free S(¾).

First claim

1 . An electrochemical method for the detection and/or quantification of sulphur dioxide (SO 2 ) in its non-complexed forms called “free” in an aqueous or hydroalcoholic liquid-food, comprising:
a) the introduction in the liquid-food of a measurement electrode of which the active surface in contact with the liquid-food is entirely in gold,
b) the measurement of the variation of the current produced by the oxidisation of the free SO 2 present in the liquid-food, during potential scanning by cyclic voltammetry.

2 . The method according to claim 1 , wherein at step b), the potential scanning can be performed between +0.1 V and +1.9 V, using an Ag/AgCl reference electrode, at potential scanning speeds comprised between 1 mV·s −1 and 10,000 mV·s −1 .

3 . The method according to claim 1 , wherein the liquid-food is wine.

4 . The method according to claim 1 , wherein the measurement electrode has a R theo ratio between its developed surface area (A dev ) and its apparent surface area (A app ) greater than or equal to 3.

5 . The method according to claim 1 , wherein the measurement electrode has a R theo ratio comprised between 3 and 100, preferably between 3 and 20.

6 . The method according to claim 1 , wherein it further comprises, prior to step b), a step b1) of potential scanning during a cyclic voltammetry, performed between +0.1 V and +1.5 V, using an Ag/AgCl reference electrode, at potential scanning speeds comprised between 1 mV·s −1 and 10,000 mV·s −1 , without a measurement of the current variation.

7 . The method according to claim 1 , wherein it further comprises:
prior to step b), a step b2) of establishing an abacus providing the pH value of the liquid-food as a function of the position of the peak of reduction of the gold oxides during potential scans by cyclic voltammetry performed in said liquid-food at different pH values, using an Ag/AgCl reference electrode, at potential scanning speeds comprised between 1 mV·s −1 and 1,000 mV·s −1 , the determination of the alcohol titration, ABV, of the liquid-food, and during step b) the measurement of the temperature T of the liquid-food, which provides the percentage of molecular SO 2 contained in the non-complexed SO 2 , thanks to the following formula:
molecular SO 2 %=100/[10 (pH−pK1 )+1]
wherein pK 1 =1.949+( T− 20)×0.0322+(ABV−10)×0.01971.

8 . A method for regenerating in the liquid-food an electrode of which the active surface is entirely in gold, wherein it comprises:
a) the introduction in the liquid-food of an electrode, of which the active surface in contact with the liquid-food is in gold, and b1) the implementation of cyclic voltammetry with potential scanning comprised between +0.1 V and +1.5 V, using an Ag/AgCl reference electrode, at potential scanning speeds comprised between 1 mV·s −1 and 10,000 mV·s −1 , without a measurement of the current variation.

9 . An electrochemical device for the detection and/or quantification of the free SO 2 in an aqueous or hydroalcoholic liquid-food, comprising:
a reference electrode a counter-electrode a measurement electrode, of which the active surface is entirely in gold, said measurement electrode having a R theo ratio between its developed surface area (A dev ) and its apparent surface area (A app ) greater than or equal to 3.

10 . The device according to claim 9 , wherein the measurement electrode is an electrode comprising a support covered with a porous sheath in gold, the sheath having a thickness and a pore size such that the measurement electrode has a R theo ratio between its developed surface area (A dev ) and its apparent surface area (A app ) greater than or equal to 3, preferably comprised between 3 and 100, and more preferably comprised between 3 and 20.

11 . The device according to claim 9 , wherein the measurement electrode is an electrode comprising a support covered with a rough layer of gold constituted of gold crystallites of nano to micrometric dimensions such that the measurement electrode has a R theo ratio between its developed surface area (A dev ) and its apparent surface area (A app ) greater than or equal to 3.

Assignees

• Univ Bordeaux
• Inst Polytechnique Bordeaux
• Centre Nat Rech Scient

Inventors

• Arbault Stéphane
• Reculusa Stéphane
• Kuhn Alexander
• Sojic Neso
• Masse Pascal

Classifications

• G01N33/0042

  SO2 or SO3 · CPC title

• G01N33/146

  containing alcohol · CPC title

• G01N27/4166

  measuring a particular property of an electrolyte · CPC title

• G01N27/48 Primary

  using polarography, i.e. measuring changes in current under a slowly-varying voltage · CPC title

• Y02A50/20

  Air quality improvement or preservation, e.g. vehicle emission control or emission reduction by using catalytic converters · CPC title