JP6576053B2 - Constant potential electrolytic gas sensor - Google Patents

Description

  In the present invention, a reaction electrode for electrochemically reacting a gas to be detected as a gas electrode for detecting gas, a counter electrode with respect to the reaction electrode, and a reference electrode for controlling the potential of the reaction electrode are brought into contact with an electrolytic solution accommodated in an electrolytic cell. The present invention relates to a constant potential electrolysis gas sensor.

  A conventional constant potential electrolytic gas sensor is configured such that an electrode is provided facing an electrolytic solution storage part of an electrolytic cell in which an electrolytic solution is densely stored. For example, an electrode is detected as a gas electrode that detects gas. There are provided three electrodes: a reaction electrode for electrochemically reacting gas, a counter electrode for the reaction electrode, and a reference electrode for controlling the potential of the reaction electrode. A potentiostat circuit for setting the potential is connected. As the material of the three electrodes, a gas-permeable porous PTFE film having water repellency is coated with a noble metal catalyst such as platinum, gold, palladium, etc. As an electrolyte, an acidic aqueous solution such as sulfuric acid or phosphoric acid is used. Was used.

  In addition, the constant potential electrolytic gas sensor generates a current corresponding to the change in the surrounding environment between the reaction electrode and the counter electrode by controlling the potential of the reaction electrode to be constant with respect to the change in the surrounding environment. . Then, by utilizing the fact that the potential of the reaction electrode does not change and the oxidation-reduction potential varies depending on the gas type, it becomes possible to selectively detect the gas depending on the set potential of the potentiostat circuit. Further, by changing the catalyst used for the gas electrode, it is possible to have high selectivity for the target gas.

  Note that the above-described constant potential electrolytic gas sensor, which is a conventional technique in the present invention, is a general technique, and therefore does not show any prior art documents such as patent documents.

  In such a constant potential electrolytic gas sensor, a pinhole directly drilled in the casing is used as a gas introduction part, and gas is introduced into the sensor via the gas introduction part. In addition, for example, a pinhole drilled at a position facing the gas introduction portion is used as a gas discharge portion, and the gas inside the sensor is discharged via the gas discharge portion.

  Usually, a reference electrode is disposed on the gas discharge part side in the electrolytic cell. If gas flows in from the pinhole of the gas discharge section and this gas comes into contact with the reference electrode, it becomes difficult to control the potential of the reaction electrode, and the output value of the sensor may become unstable.

  Accordingly, an object of the present invention is to provide a constant potential electrolytic gas sensor having a stable output value.

In order to achieve the above object, a constant potential electrolytic gas sensor according to the present invention controls a reaction electrode for electrochemically reacting a gas to be detected as a gas electrode for detecting gas, a counter electrode for the reaction electrode, and a potential of the reaction electrode. A constant potential electrolytic gas sensor provided with a reference electrode in contact with an electrolyte contained in an electrolytic cell, the first feature of which is a gas discharge that opens to the side of the electrolytic cell and discharges gas The counter electrode and the reference electrode are arranged in order from the gas discharge part side, and an interference gas blocking film for blocking interference gas is provided between the counter electrode and the reference electrode, and the interference gas blocking The membrane is an ion exchange membrane that has ionic conductivity and does not allow interference gas to pass therethrough .

  According to this configuration, the reference electrode can be disposed inside the interference gas blocking film. Therefore, even if interference gas flows in from the gas discharge part, the interference gas can be blocked by the interference gas blocking film before reaching the reference electrode, and can be prevented from coming into contact with the reference electrode. Can do.

  When oxygen gas is generated by the electrode reaction at the counter electrode, this oxygen gas needs to be discharged from the gas discharge portion. Therefore, since the interference gas blocking film is provided between the counter electrode and the reference electrode disposed on the gas discharge part side as in this configuration, there is no interference gas blocking film on the gas discharge part side in the counter electrode. The oxygen gas generated at the counter electrode can be discharged from the gas discharge section.

Therefore, according to this configuration, it is possible to prevent the interference gas flowing in from the gas discharge part from coming into contact with the reference electrode, and to discharge the oxygen gas generated at the counter electrode from the gas discharge part.
Further, if the interference gas blocking film is an ion exchange film having ionic conductivity and not allowing the interference gas to permeate, the interference gas can be effectively blocked.

  The second characteristic configuration of the constant potential electrolytic gas sensor according to the present invention is that a pore is formed in the reference electrode and the interference gas blocking film, and an electrolytic solution flows to the counter electrode side through the pore, A water retaining member that absorbs and holds the liquid is disposed between the counter electrode and the interference gas blocking film.

  According to this configuration, since the water retention member can be disposed so as to be in contact with the counter electrode, the electrolyte solution held by the water retention member and the counter electrode can be brought into contact with each other. The electrolyte solution in contact with the counter electrode is connected to the electrolyte container between the reaction electrode and the reference electrode via the pores formed in the reference electrode and the interference gas blocking film. Can be brought into contact with the electrolyte.

  A third characteristic configuration of the constant potential electrolytic gas sensor according to the present invention is that the gas discharge part is covered with a dew condensation / pressure relaxation film that prevents dew condensation.

  The condensation / pressure relaxation film can prevent the occurrence of condensation in the gas discharge portion. When the surroundings change, for example, when condensation occurs in the gas discharge unit and closes the gas discharge unit, the pressure inside the sensor is difficult to escape and the fluctuation of the indicated value may increase. Moreover, when these are completely blocked, there is a possibility that the indicated value becomes zero. However, by providing a dew condensation / pressure relaxation film as in this configuration, it is difficult for dew condensation to occur in the gas discharge section, which makes it easier for the pressure inside the sensor to escape, so the pressure rise inside the sensor can be mitigated. The indicated value is stable.

It is the schematic which shows the constant potential electrolytic gas sensor of this invention. It is the schematic which shows an opening mounting member. It is the graph which investigated the presence or absence of the influence of interference gas (hydrogen gas 5000ppm) when detecting oxygen gas (21 vol%) as to-be-detected gas.

Hereinafter, embodiments of the present invention will be described with reference to the drawings.
As shown in FIG. 1, the constant potential electrolytic gas sensor X controls a reaction electrode 11 that causes a gas to be detected to electrochemically react as a gas electrode 10 that detects gas, a counter electrode 12 with respect to the reaction electrode 11, and a potential of the reaction electrode 11. The reference electrode 13 is provided so as to be in contact with the electrolytic solution 20 accommodated in the electrolytic cell 30. The constant potential electrolytic gas sensor X includes a gas introduction part 32 that opens to the side of the electrolytic cell 30 and introduces gas, and a gas discharge part 33 that opens to the side of the electrolytic cell 30 and discharges gas. I have.

  The reaction electrode 11, the counter electrode 12, and the reference electrode 13 are formed by applying and baking a paste made of a known electrode material on the surface of a porous gas permeable film 14 having water repellency. The gas permeable membrane 14 may be any membrane as long as it is hydrophobic and has a property of transmitting gas. For example, a porous PTFE (polytetrafluoroethylene) membrane having chemical resistance may be used. it can. The reaction electrode 11 and the reference electrode 13 are arranged to face each other, and the counter electrode 12 and the reference electrode 13 are arranged in this order from the gas discharge part 33 side. A space between the reaction electrode 11 and the reference electrode 13 serves as an electrolyte solution storage unit 31 that stores the electrolyte solution 20. The electrolytic solution 20 may be an acidic aqueous solution such as sulfuric acid or phosphoric acid, but is not limited thereto. The gas to be detected is introduced into the sensor from the gas introduction part 32 and reacts on the reaction electrode 11.

Each gas electrode 10, gas permeable membrane 14, dissolved oxygen barrier film 41, interference gas barrier film 42, O-ring 15 a and gasket 15 b are fixed by the lid member 16 of the electrolytic cell 30. The dissolved oxygen blocking film 41 is provided on the reaction electrode 11 on the side of the electrolytic solution 20 in order to block oxygen dissolved in the electrolytic solution 20 (dissolved oxygen). Further, the interference gas blocking film 42 is provided between the counter electrode 12 and the reference electrode 13 in order to block interference gas.
The reaction electrode 11, the counter electrode 12, and the reference electrode 13 are composed of a gas diffusion electrode containing a catalyst and a hydrophobic resin. Examples of the catalyst include platinum (Pt), gold (Au), ruthenium (Ru), ruthenium oxide (RuO2), Palladium (Pd), platinum-supported carbon (Pt / C) and the like are preferably used, and a porous PTFE membrane and the like are preferably used as the hydrophobic resin.

  An internal pressure adjusting hole 17 having a small diameter of about 0.5 to 1 mm is formed at one end of the electrolytic cell 30. A porous sheet 18 is disposed on the internal pressure adjusting hole 17 on the side of the electrolytic solution containing portion 31. The electrolyte storage unit 31 has two large-diameter storage units 31b through a small-diameter channel 31a. When the flow path 31a has a small diameter of about 2 to 4 mm, the electrolytic solution 20 is less likely to flow backward from one housing portion 31b to the other housing portion 31b due to the surface tension of the electrolytic solution 20. The electrolytic cell 30 and the lid member 16 constituting the housing may be made of a synthetic resin having corrosion resistance, for example, a metal such as hard vinyl chloride or nickel alloy.

  A water retention member 37 that absorbs and holds the electrolytic solution 20 can be disposed in the electrolytic solution storage unit 31. This configuration will be described later.

  Such a constant potential electrolytic gas sensor X includes a current measuring unit capable of detecting a current based on electrons generated on the reaction electrode 11 due to a reaction of the gas to be detected, and a potential control unit capable of controlling the potential of the reaction electrode 11. It is used as a gas detection device by connecting to a gas detection circuit (not shown). The constant potential electrolytic gas sensor X of the present invention is used for detecting oxygen gas, hydride gas such as silane, phosphine, germane, arsine and diborane, and detecting toxic gas such as carbon monoxide and hydrogen sulfide. In the present embodiment, a case where oxygen gas is detected as the gas to be detected will be described.

(Opening mounting member)
At least one of the gas introduction part 32 and the gas discharge part 33 is an opening mounting member 36 in which a cylindrical member 34 made of metal oxide and formed with a pinhole 34a is press-fitted into an elastic member 35 made of resin. (Fig. 2).

  The opening mounting member 36 may be provided in at least one of the gas introduction part 32 and the gas discharge part 33. In the present embodiment, the case where the opening attachment member 36 is provided in both the gas introduction part 32 and the gas discharge part 33 will be described. The opening mounting member 36 is inserted into a through hole 16 a formed in the lid member 16 constituting the housing and fixed to the lid member 16.

  The opening mounting member 36 of the present embodiment includes a columnar part 36a through which the cylindrical member 34 penetrates, a plate-like part 36b provided on one end side of the columnar part 36a, and a return part 36c provided on the other end side of the columnar part 36a. And comprising. The opening mounting member 36 can be brought into surface contact with the housing (lid member 16) by the plate-like portion 36b and can be fixed securely. Moreover, it is possible to prevent the opening mounting member 36 from falling out of the through hole 16a formed in the housing (the lid member 16) by the return portion 36c. What is necessary is just to insert the opening mounting member 36 so that it may press-fit with respect to the said through-hole 16a.

  Examples of the metal oxide constituting the cylindrical member 34 include, but are not limited to, ceramics such as alumina and zirconia. The long dimension of the cylindrical member is 0.5 to 6.0 mm, preferably 1.5 to 5.5 mm. Moreover, the hole diameter of the pinhole 34a is 8-200 micrometers, Preferably it is 12-125 micrometers.

  The shape of the cylindrical member 34 is preferably a columnar shape, but is not limited thereto, and may be an aspect such as a prismatic shape.

  The elastic member 35 may be formed of a material having elasticity, for example, a rubber-like elastic material used for packing, a thermoplastic elastomer, or the like. A through hole 35a having a smaller diameter than the outer diameter of the cylindrical member 34 is formed in the elastic member 35, and the cylindrical member 34 is press-fitted into the through hole 35a.

  One or more pinholes 34a may be provided in the cylindrical member 34. What is necessary is just to set suitably about the number of the pinholes 34a according to the quantity of to-be-detected gas to introduce | transduce into a sensor. In the present embodiment, a case where one pinhole 34a is formed in each cylindrical member 34 will be described.

(Condensation / pressure relief membrane)
In a state where the opening mounting member 36 is inserted into the through hole 16 a formed in the lid member 16, a dew condensation / pressure relaxation film 40 for preventing condensation is disposed so as to cover the opening mounting member 36 from both sides. That is, the dew condensation / pressure relaxation film 40 is disposed so as to cover the gas introduction part 32 and the gas discharge part 33. In this embodiment, the dew condensation / pressure relaxation film 40 covers both the gas introduction part 32 and the gas discharge part 33. However, the dew condensation / pressure relaxation film 40 is at least a gas introduction in the gas introduction part 32 and the gas discharge part 33. Any mode that covers the portion 32 may be used.

  The condensation / pressure relaxation film 40 can prevent the occurrence of condensation in the gas introduction part 32 or the gas discharge part 33 provided with the film. For example, when dew condensation occurs in the gas introduction unit 32 due to changes in the surrounding environment, there is a possibility that the gas to be detected cannot be introduced into the sensor. In addition, when the gas inlet 32 and the gas outlet 33 are blocked by the condensation, the pressure inside the sensor is difficult to be released and the fluctuation of the indicated value may increase. Moreover, when these are completely blocked, there is a possibility that the indicated value becomes zero. However, the provision of the dew condensation / pressure relaxation film 40 makes it difficult for dew condensation to occur in the gas introduction part 32 and the gas discharge part 33 having the opening mounting member 36 having the fine pinhole 34a, and the detected gas is supplied to the sensor. It can be prevented from being introduced into the inside, and the pressure dependence (especially sudden pressure rise) inside the sensor can be mitigated to reduce the pressure dependence, and the indicated value is also stabilized.

  The dew condensation / pressure relaxation film 40 may be any film as long as it has a property of permeating gas but not liquid, and a porous PTFE film or the like can be used.

  The dew condensation / pressure relief film 40 of this embodiment has a thickness of about 0.2 mm, and its characteristics are, for example, an air permeability of about 200 to 700 in terms of Gurley value, a porosity of 35 to 45%, and WEP (water intrusion). The pressure) is 196 kPa or more, preferably 500 kPa.

  Further, in the present embodiment, a case will be described in which a set of two dew condensation / pressure relaxation films 40 having different air permeability is disposed at least in the gas introduction part 32 in the gas introduction part 32 and the gas discharge part 33.

The dew condensation / pressure relaxation film 40 may be a single layer film, may be formed by stacking two films having the same air permeability, or may be formed by stacking two films having different air permeability. May be.
For example, in the case where two dew condensation / pressure relaxation films 40 are stacked and disposed in at least the gas introduction part 32, the above-described air permeability and WEP film may be two sheets, or one film may have the above air permeability and A film having WEP may be used, and the other film may be a film having a lower value than the above-described air permeability and WEP. The other film may be any film (for example, having water repellency) that can press and adhere one film and prevent the electrolyte solution 20 from leaking from the reaction electrode 11. For example, in the case of the gas introduction part 32, the reaction electrode 11, the other film, the one film, and the cylindrical member 34 (pin) Hole 34a) can be used. The two layers of the dew condensation / pressure relaxation film 40 may be disposed on the outer side and the inner side of the opening mounting member 36 (FIG. 1), or may be disposed only on either the outer side or the inner side. Although it is good, when arrange | positioning only in any one, disposing outside is preferable.

(Dissolved oxygen barrier membrane)
The dissolved oxygen blocking film 41 described above is provided on the side of the electrolytic solution 20 in the reaction electrode 11 in order to block oxygen dissolved in the electrolytic solution 20 (dissolved oxygen). The dissolved oxygen blocking film 41 is preferably provided on the entire surface of the reaction electrode 11 on the side of the electrolytic solution 20.

  The dissolved oxygen blocking film 41 may be an ion exchange membrane that has ionic conductivity and water permeability and does not allow oxygen gas to permeate. Specifically, Nafion (registered trademark: manufactured by DuPont), Aciplex (registered trademark: manufactured by Asahi Kasei Co., Ltd.), Flemion (registered trademark: manufactured by Asahi Glass Co., Ltd.) and the like can be used as the dissolved oxygen barrier film 41. However, the present invention is not limited to this. For example, Nafion has proton conductivity and water permeability and is excellent in oxidation resistance.

Since the dissolved oxygen barrier film 41 has ionic conductivity and water permeability, H ⁺ and H ₂ O molecules can move to the reaction electrode 11 through the dissolved oxygen barrier film 41 from the electrolyte solution 20 side. The electrode reaction field in the constant potential electrolytic gas sensor X can be the surface of the reaction electrode 11.

  The dissolved oxygen blocking film 41 can be thermocompression bonded to the reaction electrode 11. In order to block dissolved oxygen, there is an effect even when a solution containing a component constituting the dissolved oxygen blocking film 41 is applied to the reaction electrode 11 and dried, but the dissolved oxygen blocking film 41 is further thermocompression bonded. By forming, it becomes more effective.

  Specifically, in the thermocompression bonding, a solution containing components constituting the dissolved oxygen blocking film 41 is applied to the surface of the reaction electrode 11 (application process), the solution is applied and dried, and then the lead wire is applied. After the dissolved oxygen blocking film 41 is stacked in a state of being placed on the reaction electrode 11 and the dissolved oxygen blocking film 41 is stacked (stacking step), it is thermocompression-bonded at 120 to 140 ° C., preferably 130 ° C. and 1 to 4 MPa (thermal). Crimping process).

  When the dissolved oxygen blocking film 41 is Nafion, a Nafion solution is applied to the surface of the reaction electrode 11 (application process). The concentration of the Nafion solution is 5 to 20 wt%, and the solvent may be a mixture of lower alcohol and pure water (15 to 34%) or pure water.

  Thus, by stacking Nafion with the lead wire placed on the reaction electrode 11, current collection between the lead wire and the reaction electrode 11 can be ensured.

(Interference gas barrier film)
The interference gas blocking film 42 described above is provided between the counter electrode 12 and the reference electrode 13 in order to block interference gas. The interference gas is a gas that coexists with the gas to be detected in the sampling gas and affects the detected gas detection value. The interference gas blocking film 42 may be, for example, an ion exchange film having ion conductivity and water permeability and not allowing interference gas to pass therethrough, but is not limited to such a film, and is a film such as PET, PP, PE, etc. Can also be used. Specifically, Nafion etc. mentioned above can be used, but it is not limited to this.

  If an interference gas flows in from the gas discharge part 33 and this interference gas contacts the reference electrode 13, the potential of the reaction electrode 11 becomes difficult to control, and the sensor output value may not be stable. In this configuration, the counter electrode 12 and the reference electrode 13 are arranged in this order from the gas discharge part 33 side, and since the interference gas blocking film 42 is provided between the counter electrode 12 and the reference electrode 13, the reference electrode 13 is blocked from the interference gas. It can be arranged inside the membrane 42 (on the side of the electrolyte container 31). Therefore, the interference gas flowing in from the gas discharge part 33 can be blocked by the interference gas blocking film 42 before reaching the reference electrode 13, and can be prevented from coming into contact with the reference electrode 13 in advance.

  When oxygen gas is generated by the electrode reaction at the counter electrode 12, this oxygen gas needs to be discharged from the gas discharge portion 33. For this reason, when the interference gas blocking film 42 is provided on the gas discharge portion 33 side of the counter electrode 12, the oxygen gas cannot be discharged from the gas discharge portion 33. Therefore, as in the present configuration, the interference gas blocking film 42 is provided between the counter electrode 12 and the reference electrode 13 disposed on the gas discharge part 33 side, so that the interference gas is provided on the gas discharge part 33 side of the counter electrode 12. Since the blocking film 42 does not exist, the oxygen gas generated at the counter electrode 12 can be discharged from the gas discharge unit 33.

  The reference electrode 13 and the interference gas blocking film 42 are formed with pores 13a and 42a, respectively, and the electrolytic solution 20 is circulated to the counter electrode 12 through the pores 13a and 42a. At this time, a water retaining member 37 that absorbs and holds the electrolytic solution 20 may be disposed between the counter electrode 12 and the interference gas blocking film 42. The diameter of the pores 13a and 42a may be about 2 mm.

  In this configuration, since the water retaining member 37 can be disposed so as to be in contact with the counter electrode 12, the electrolytic solution 20 held by the water retaining member 37 and the counter electrode 12 can be brought into contact with each other. The electrolyte 20 in contact with the counter electrode 12 is connected to the electrolyte container 31 between the reaction electrode 11 and the reference electrode 13 through the pores 13 a and 42 a formed in the reference electrode 13 and the interference gas blocking film 42. Therefore, all of the three gas electrodes 10 can be brought into contact with the electrolytic solution 20.

(Water retaining material)
The water retaining member 37 is not particularly limited as long as it is a water absorbing member capable of holding the electrolytic solution 20 such as a water retaining fiber (for example, glass fiber, ceramic fiber, etc.) or a water absorbing polymer.
Moreover, the water retaining member 37 may be filled in the entire surface of one accommodating portion 31b (the side on which the gas electrode 10 is disposed) in the electrolyte accommodating portion 31 as in the present embodiment. As a result, bubbles generated by electrode reactions at each gas electrode, air dissolved in the electrolyte due to a rapid temperature change, or direct intrusion of air in a sudden pressurization state It is possible to avoid that the surfaces of the two gas electrodes 10 are covered with air (the reaction area of the electrodes is reduced and the indication may become unstable).

[Another embodiment]
In the above-described embodiment, the water retaining member 37 that absorbs and holds the electrolytic solution 20 is disposed between the counter electrode 12 and the interference gas blocking film 42, or the entire surface of one accommodating portion 31 b in the electrolytic solution accommodating portion 31. Although filled, the water retaining member 37 may be disposed in a part of the electrolytic solution storage unit 31. In this case, a plurality of water retaining members 37 may be provided between the reaction electrode 11 and the reference electrode 13 separately on the reaction electrode 11 side and the reference electrode 13 side. At this time, it is possible to provide a holding member 50 that presses these water retaining members 37 against the reaction electrode 11 and the reference electrode 13 separately (FIGS. 3 and 4). The pressing force with which the pressing member 50 presses the water retaining member 37 against the reaction electrode 11 and the reference electrode 13 can be set according to the material and shape of the pressing member 50.

  What is necessary is just to comprise the water retention member 37 so that the thickness may be fluctuate | varied with the pressing force by the pressing member 50. FIG. Also in this configuration, the water retaining member 37 may be a water absorbing member capable of holding the electrolytic solution 20 as described above, and is used without any particular limitation, such as a water retaining fiber, a water absorbing polymer, or the like. Can do.

  The water retaining member 37 may be disposed so as to cover the entire surface of the reaction electrode 11 and the reference electrode 13.

  The pressing member 50 is configured to include an elastically deformable core member 51 and perforated plate-like members 52 disposed at both ends of the core member 51. The pressing member 50 can be made of a resin such as hard vinyl chloride having chemical resistance, but is not limited to this. By manufacturing with such resin, the core member 51 can be configured to be elastically deformable.

  In the present embodiment, four plate member openings 52a are provided in the plate member 52, but the present invention is not limited to this. The number of the plate-like member openings 52a may be appropriately set in consideration of the surface tension of the electrolytic solution 20, the water absorption of the water retaining member 37, and the like.

  Further, in order to configure the core member 51 so as to be elastically deformable, the core member 51 may be configured with a spring material.

  The pressing member 50 is preferably arranged so that the core member 51 is at a position corresponding to the gas introduction part 32.

  The performance of each of the controlled potential electrolytic gas sensor X of the present invention and the conventional controlled potential electrolytic gas sensor (comparative example) was compared. The constant potential electrolysis gas sensor X of the present invention is provided with the interference gas blocking film 42 (Nafion), and the conventional constant potential electrolysis gas sensor is not provided with the interference gas blocking film 42. Each sensor used four sensors, and when oxygen gas (21 vol%) was detected as the gas to be detected, the presence or absence of detection (influence) of interference gas (hydrogen gas 5000 ppm) was examined. The results are shown in FIG.

  As a result, in the conventional constant potential electrolytic gas sensor, the indicated value when oxygen gas was detected was not stable, and it was recognized that the influence of the interference gas was great. On the other hand, in the controlled potential electrolysis gas sensor X of the present invention, the indicated value when oxygen gas was detected was stable, and the influence of the interference gas was hardly recognized.

  In the present invention, a reaction electrode for electrochemically reacting a gas to be detected as a gas electrode for detecting gas, a counter electrode with respect to the reaction electrode, and a reference electrode for controlling the potential of the reaction electrode are brought into contact with an electrolytic solution accommodated in an electrolytic cell. It can utilize for the constant potential electrolytic gas sensor provided.

X Constant Potential Electrolytic Gas Sensor 10 Gas Electrode 11 Reaction Electrode 12 Counter Electrode 13 Reference Electrode 13a Pore 20 Electrolytic Solution 30 Electrolytic Tank 33 Gas Discharge Part 37 Water Retaining Member 40 Condensation / Pressure Relaxation Film 42 Interference Gas Blocking Film 42a Pore

Claims (3)

As a gas electrode for detecting gas, a reaction electrode for electrochemically reacting a gas to be detected, a counter electrode for the reaction electrode, and a reference electrode for controlling the potential of the reaction electrode were provided so as to come into contact with an electrolytic solution contained in an electrolytic cell. A constant potential electrolytic gas sensor,
A gas discharge part that opens to the side of the electrolytic cell and discharges the gas;
In order from the side of the gas discharge part, the counter electrode and the reference electrode are disposed,
Between the counter electrode and the reference electrode, an interference gas blocking film for blocking interference gas is provided ,
The constant potential electrolytic gas sensor, wherein the interference gas blocking film is an ion exchange film having ion conductivity and not allowing interference gas to permeate . A pore is formed in the reference electrode and the interference gas blocking film, and an electrolyte flows through the pore to the counter electrode side,
The constant potential electrolytic gas sensor according to claim 1, wherein a water retention member that absorbs and retains the electrolytic solution is disposed between the counter electrode and the interference gas blocking film.   The constant potential electrolytic gas sensor according to claim 1 or 2, wherein the gas discharge part is covered with a condensation / pressure relaxation film that prevents condensation.

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