The method describes how to determine the oxygen content in water using a WTW measuring device.
If an electrode system, usually consisting of a gold cathode and a silver anode, is polarized under suitable conditions, any oxygen present in solution is reduced. The change in the polarization voltage that takes place as this occurs is directly proportional to the partial pressure of the oxygen (according to CLARK). The partial pressure and the volume of the gas are also proportional.
The method describes how to determine the oxygen content of water using an Orbisphere meter.
An electrochemical cell consisting of two electrodes and electrolytes, and that is covered with a membrane permeable to oxygen, produces an electric current. The current is proportional to the permeability of the membrane to oxygen, i.e., proportional to the partial pressure of oxygen in the medium. Oxygen reacts at the cathode of the cell, which normally consists of a precious metal (e.g., gold), according to the following equation:
O2 + 2 H2O + 4 e- → 4 OH-
in which e- means one electron in the metal. The electron flux over the course of the reaction produces the current that is then measured. In addition, the temperature also has an impact on the amount of current, which can be compensated for electronically.
This describes how to determine the oxygen content in water according to the TÖDT and TESKE method.
The measurement using the Digox Analyzer occurs without a membrane using the potentiostatic 3-electrode measuring system according to TÖDT und TESKE.
The cathode performing the measurement consists of solid silver, while the anode is made of stainless steel and serves as an auxiliary electrode. The reference electrode consists of silver/silver chloride.
An electrochemical reaction occurs after applying a defined polarization voltage at the cathode. The oxygen molecules are reduced in this reaction.
Cathode (silver):
O2 + 2 H2O + 4 e- → 4 OH- (cathodic process)
Auxiliary electrode (VA):
4 OH- → O2 + 2 H2O + 4 e- (anodic process)
After a specific polarization voltage is applied, an electrochemical reaction takes place at the cathode. The current flowing while the reaction is taking place is directly proportional to the quantity of dissolved oxygen, i.e., if the polarization voltage remains as precise as possible at the level of the diffusion limited current.
If this is the case, the relationship is represented as follows:
I = K × CO2, where K = n × F × A × 1/d
I = current measured
CO2 = oxygen concentration
n = number of electrons exchanged per molecule
F = Faraday constant
A = cathode surface
d = thickness of the natural convection boundary layer
The thickness of the natural convection boundary layer is defined by the hydrodynamic conditions at the cathode, while the movement of oxygen molecules through the barrier layer is determined by temperature-dependent diffusion processes. Those two clearly defined factors are measured precisely and are taken into consideration.
In order to adjust the polarization voltage between both electrodes in a defined manner, a third electrode, the auxiliary electrode, is employed for DIGOX analyzers. This auxiliary electrode remains in electrolytic contact with the surface of the cathode by means of a diaphragm but without the possibility of a mass transfer.
This method describes how to determine the foam stability by means of the Ross and Clark method.
beer and beer-based beverages
CO2 is introduced into the beer so that a specific volume of foam is produced. The mean retention time of the bubbles in the foam serves as a measure for the foam stability, which is calculated as the relationship between the time required for the foam to collapse and the logarithm of the relationship between the volume of the collapsed foam and the foam still present [1–3].
This method is frequently applied in instances when the influence of carbon dioxide content on foam formation in the beer is to be eliminated.
Determination of the concentration of dissolved oxygen through electrochemical oxygen sensors with membrane-enveloped electrodes
The analytical determination of oxygen using amperometric electrodes is achieved through measurement of the electrical current. The electrodes consist of a cathode and an anode, which are connected conductively through an electrolyte solution (KCl/KOH). Precious metals, such as platinum and gold are chosen for the cathode, and silver, for the anode. The gas-permeable membrane separates the two electrodes from the solution being measured. An appropriate polarization voltage causes diffusion of the oxygen across the membrane into the measurement cell, where it reaches the surface of the cathode and is reduced, producing hydroxide ions.
Reaction at the cathode: O2 + 4e– + 2 H2O → 4 OH−
Reaction at the anode: 4 Ag + 4 Cl− → 4 AgCI + 4e−
This chemical reaction creates an electrical current that is proportional to the partial pressure pO2 of the oxygen. Oxygen must be steadily liberated from the solution being measured for the oxygen electrode to receive a constant supply. The concentration of oxygen in the medium can be determined using HENRY’s law and the solubility coefficient of oxygen [1]. Three different variations on the types of the equipment required for performing this analysis are present below.