US20050158457A1 - Sensor for determining gases and method for manufacturing the sensor - Google Patents

Sensor for determining gases and method for manufacturing the sensor Download PDF

Info

Publication number
US20050158457A1
US20050158457A1 US11/000,387 US38704A US2005158457A1 US 20050158457 A1 US20050158457 A1 US 20050158457A1 US 38704 A US38704 A US 38704A US 2005158457 A1 US2005158457 A1 US 2005158457A1
Authority
US
United States
Prior art keywords
sensor
polymer layer
sensor according
electrode
electrodes
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US11/000,387
Inventor
Thomas Brinz
Jane Lewis
Claus Heppel
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Robert Bosch GmbH
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Assigned to ROBERT BOSCH GMBH reassignment ROBERT BOSCH GMBH ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: HEPPEL, CLAUS, BRINZ, THOMAS, LEWIS, JANE
Publication of US20050158457A1 publication Critical patent/US20050158457A1/en
Priority to US12/418,150 priority Critical patent/US8758585B2/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N27/00Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
    • G01N27/26Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
    • G01N27/416Systems
    • G01N27/4166Systems measuring a particular property of an electrolyte
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/0004Gaseous mixtures, e.g. polluted air
    • G01N33/0009General constructional details of gas analysers, e.g. portable test equipment
    • G01N33/0027General constructional details of gas analysers, e.g. portable test equipment concerning the detector
    • G01N33/0036Specially adapted to detect a particular component
    • G01N33/004Specially adapted to detect a particular component for CO, CO2

Definitions

  • Optical sensors for determining the carbon dioxide content of the air are used, among other things, in fire detectors. Their function is based on the fact that a layer sensitive to carbon dioxide changes color reversibly upon contact with the gas to be determined. This change of color is monitored by a detector, and when a predetermined minimum concentration is exceeded, an alarm is triggered. This measuring method is relatively susceptible to contamination.
  • Optical CO 2 gas sensors normally are made up of a polymeric matrix, e.g. ethylcellulose, a softener and solutizer, e.g. Brij 30, and a basic gas acceptor, e.g. tetraoctylammonium hydroxide.
  • a polymeric matrix e.g. ethylcellulose
  • softener and solutizer e.g. Brij 30
  • a basic gas acceptor e.g. tetraoctylammonium hydroxide
  • U.S. Pat. No. 6,241,873 describes a carbon dioxide sensor which detects the carbon dioxide content of a surrounding atmosphere in a potentiometric manner. It features a measuring electrode and a reference electrode, which are applied on a substrate.
  • the measuring electrode takes the form of a silver/silver carbonate electrode.
  • the potential of this electrode is a direct function of the carbon dioxide concentration of the surroundings.
  • a disadvantage of this measuring method is the fact that carbonate-containing electrodes are affected by weather influences and thus have only a low stability. Furthermore, the sensor is limited to measuring carbon dioxide.
  • the present invention is based on the objective of providing a gas sensor for determining different gases in a potentiometric and/or optical manner, which has a high stability and at the same time a high sensitivity.
  • a further objective lies in the compensation of the moisture-dependency of the sensor.
  • the sensor according to the present invention has the advantage that its electrodes are stable over the long term and that its measuring electrode has a high sensitivity with respect to the gas to be determined. This is achieved in that a pH-sensitive electrode is used that detects the pH value of a surrounding polymer. Such pH electrodes have a sufficiently long service life and allow for the determination of various acidic and basic gases.
  • the senor can be designed in such a way that, in addition to measuring the pH value, the optical absorption and the conductivity can be measured as well.
  • An iridium oxide electrode is particularly suited as a measuring electrode since it is especially robust with respect to environmental influences and does not have to be provided in a pre-expanded state as do comparable glass electrodes.
  • the senor includes a polymer that has a base or an acid since this results in a quick and effective absorption of the acidic or basic gas to be determined. This further raises the sensitivity and lowers the response time of the sensor.
  • FIG. 1 shows a schematic representation of an exemplary embodiment of the sensor according to the present invention in top view.
  • FIG. 2 shows a sectional view through the sensor represented in FIG. 1 along the sectional line A-A.
  • FIG. 3 shows a schematic representation of another exemplary embodiment of the sensor according to the present invention.
  • Sensor 10 represented in FIGS. 1 and 2 includes a substrate 12 preferably made of a ceramic material such as aluminum oxide for example.
  • a measuring electrode 14 preferably in the form of a so-called interdigital electrode, is provided. This forms a comb-like structure.
  • a reference electrode 16 is situated on the substrate which preferably also takes the form of an interdigital electrode, the extensions of comb-like reference electrode 16 engaging with the extensions of the comb-like measuring electrode 14 . This ensures a small distance between the measuring electrode 14 and the reference electrode 16 and thus a low impedance of the sensor and at the same time a large electrode surface.
  • Electrodes 14 , 16 are connected to contact surfaces 18 , 20 via circuit traces 22 , 24 , which are preferably formed by a precious metal-containing hardenable resin such as for example a silver-containing epoxy resin.
  • Electrodes 14 , 16 are preferably coated completely by a gas-sensitive and gas-permeable polymer layer 26 , which functions as an electrolyte and which is represented in FIG. 1 as a dashed region.
  • Polymer layer 26 forms a matrix in which there are the compounds responsible for the sensitivity of the sensor.
  • polymer layer 26 is made of a hydrogel or an ethylcellulose gel. Water is irreversibly bound in these gels.
  • the mode of operation of the sensor is based on the fact that a gas to be determined, for example carbon dioxide, is absorbed by polymer layer 26 .
  • the gas dissolves in the bound water of polymer layer 26 and changes the pH value of the latter.
  • a pH sensitive electrode is used as measuring electrode 14 , the change of the pH value results in a change of the potential at measuring electrode 14 .
  • the change in potential can be measured as a changing voltage between measuring electrode 14 and reference electrode 16 .
  • Measuring electrode 14 can take on any specific embodiment that is suited for detecting a change in the pH value of the surroundings with sufficient precision.
  • conductive metal oxide pH electrodes that have for example a surface layer of mixed iridium oxides (IrO 2 ) or ruthenium oxides (RuO x ).
  • IrO 2 mixed iridium oxides
  • RuO x ruthenium oxides
  • platinum and rhodium electrodes are suitable as well.
  • FIG. 3 shows another possible specific embodiment of the sensor according to the present invention.
  • the moisture content can be determined by measuring the conductivity of the polymer film. Since the signal for the CO 2 concentration is a function of the moisture content, by also taking the moisture content into consideration, this system is able to determine the CO 2 content more exactly, i.e. without the influence of moisture.
  • the construction shown in FIG. 3 is used for this purpose.
  • the voltage drop U produced by the potential difference of the sensor is measured.
  • the two switches 30 , 32 it is possible to determine the conductivity or the resistance of the sensor element by applying a voltage (DC or AC voltage) and by measuring the current flowing through.
  • a voltage DC or AC voltage
  • the latter In order to be able to absorb acidic gases—that is, gases such as carbon dioxide, nitrogen oxides or sulfur oxides which in contact with water result in an acidic solution—as quickly as possible and in sufficient quantity in polymer layer 26 , the latter preferably contains a strong base such as tetraalkyl ammonium hydroxides or tetraalkyl ammonium hydrogen carbonates. These increase the solubility of the acidic gases in water that is bound in polymer layer 26 by removing the acid produced in the dissolving process.
  • a strong base such as tetraalkyl ammonium hydroxides or tetraalkyl ammonium hydrogen carbonates.
  • an acid such as a sulphonic acid, for example, is preferably added to polymer layer 26 .
  • This promotes the solubility of basic gases in polymer layer 26 .
  • polymer layer 26 may contain homogenization agents such as tensides for example.
  • an electrode paste preferably containing ceramic and metallic components, a so-called cermet, is applied onto substrate 12 and is sintered with the ceramic substrate 12 .
  • Polymer layer 26 is applied onto the electrode set-up in that a solution containing the polymer, a base or acid and other additives is deposited or imprinted and the solvent is removed.
  • the polymer layer has a layer thickness of 10 to 100 ⁇ m, preferably between 20 and 40 ⁇ m.
  • Electrodes 14 , 16 are contacted via circuit traces 22 , 24 , which are either formed also as cermet in one step together with electrodes 14 , 16 or by imprinting a solution containing a hardenable resin and a precious-metal component and subsequent hardening of the solution.
  • a silver-containing epoxy resin is preferred.
  • the present invention is not limited to the exemplary embodiment described, but other specific embodiments in addition to the sensor described are conceivable as well.
  • an activated carbon layer can be provided on polymer layer 26 to prevent the entry of gases that damage polymer layer 26 such as nitrogen oxides or sulfur oxides.
  • a temperature measuring unit may be additionally provided for compensating temperature influences on the measured potential differences.

Abstract

A sensor for determining the concentration of a gas in gas mixtures, which has a measuring and a reference electrode as well as a polymer layer, which is in contact with the gas mixture and with the measuring electrode. A pH sensitive electrode is provided as the measuring electrode.

Description

    BACKGROUND INFORMATION
  • Optical sensors for determining the carbon dioxide content of the air are used, among other things, in fire detectors. Their function is based on the fact that a layer sensitive to carbon dioxide changes color reversibly upon contact with the gas to be determined. This change of color is monitored by a detector, and when a predetermined minimum concentration is exceeded, an alarm is triggered. This measuring method is relatively susceptible to contamination.
  • Optical CO2 gas sensors normally are made up of a polymeric matrix, e.g. ethylcellulose, a softener and solutizer, e.g. Brij 30, and a basic gas acceptor, e.g. tetraoctylammonium hydroxide. The sensor signal reveals a dependency on the moisture content of the surroundings.
  • U.S. Pat. No. 6,241,873 describes a carbon dioxide sensor which detects the carbon dioxide content of a surrounding atmosphere in a potentiometric manner. It features a measuring electrode and a reference electrode, which are applied on a substrate. The measuring electrode takes the form of a silver/silver carbonate electrode. The potential of this electrode is a direct function of the carbon dioxide concentration of the surroundings. A disadvantage of this measuring method is the fact that carbonate-containing electrodes are affected by weather influences and thus have only a low stability. Furthermore, the sensor is limited to measuring carbon dioxide.
  • The present invention is based on the objective of providing a gas sensor for determining different gases in a potentiometric and/or optical manner, which has a high stability and at the same time a high sensitivity.
  • A further objective lies in the compensation of the moisture-dependency of the sensor.
  • SUMMARY OF THE INVENTION
  • The sensor according to the present invention has the advantage that its electrodes are stable over the long term and that its measuring electrode has a high sensitivity with respect to the gas to be determined. This is achieved in that a pH-sensitive electrode is used that detects the pH value of a surrounding polymer. Such pH electrodes have a sufficiently long service life and allow for the determination of various acidic and basic gases.
  • Thus, for example, the sensor can be designed in such a way that, in addition to measuring the pH value, the optical absorption and the conductivity can be measured as well.
  • An iridium oxide electrode is particularly suited as a measuring electrode since it is especially robust with respect to environmental influences and does not have to be provided in a pre-expanded state as do comparable glass electrodes.
  • In a particularly advantageous embodiment, the sensor includes a polymer that has a base or an acid since this results in a quick and effective absorption of the acidic or basic gas to be determined. This further raises the sensitivity and lowers the response time of the sensor.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 shows a schematic representation of an exemplary embodiment of the sensor according to the present invention in top view.
  • FIG. 2 shows a sectional view through the sensor represented in FIG. 1 along the sectional line A-A.
  • FIG. 3 shows a schematic representation of another exemplary embodiment of the sensor according to the present invention.
  • DETAILED DESCRIPTION
  • Sensor 10 represented in FIGS. 1 and 2 includes a substrate 12 preferably made of a ceramic material such as aluminum oxide for example. On top of this, a measuring electrode 14, preferably in the form of a so-called interdigital electrode, is provided. This forms a comb-like structure. Furthermore, a reference electrode 16 is situated on the substrate which preferably also takes the form of an interdigital electrode, the extensions of comb-like reference electrode 16 engaging with the extensions of the comb-like measuring electrode 14. This ensures a small distance between the measuring electrode 14 and the reference electrode 16 and thus a low impedance of the sensor and at the same time a large electrode surface. A conventional silver/silver chloride electrode is used as a reference electrode, although other electrodes of constant potential such as calomel, antimony or silver/silver bromide electrodes are suitable as well. Electrodes 14, 16 are connected to contact surfaces 18, 20 via circuit traces 22, 24, which are preferably formed by a precious metal-containing hardenable resin such as for example a silver-containing epoxy resin.
  • Electrodes 14, 16 are preferably coated completely by a gas-sensitive and gas-permeable polymer layer 26, which functions as an electrolyte and which is represented in FIG. 1 as a dashed region. Polymer layer 26 forms a matrix in which there are the compounds responsible for the sensitivity of the sensor. In a preferred embodiment, polymer layer 26 is made of a hydrogel or an ethylcellulose gel. Water is irreversibly bound in these gels.
  • The mode of operation of the sensor is based on the fact that a gas to be determined, for example carbon dioxide, is absorbed by polymer layer 26. The gas dissolves in the bound water of polymer layer 26 and changes the pH value of the latter. Since a pH sensitive electrode is used as measuring electrode 14, the change of the pH value results in a change of the potential at measuring electrode 14. The change in potential can be measured as a changing voltage between measuring electrode 14 and reference electrode 16. Measuring electrode 14 can take on any specific embodiment that is suited for detecting a change in the pH value of the surroundings with sufficient precision. Especially suited are conductive metal oxide pH electrodes that have for example a surface layer of mixed iridium oxides (IrO2) or ruthenium oxides (RuOx). However, platinum and rhodium electrodes are suitable as well.
  • FIG. 3 shows another possible specific embodiment of the sensor according to the present invention. The moisture content can be determined by measuring the conductivity of the polymer film. Since the signal for the CO2 concentration is a function of the moisture content, by also taking the moisture content into consideration, this system is able to determine the CO2 content more exactly, i.e. without the influence of moisture. The construction shown in FIG. 3 is used for this purpose.
  • At a high-impedance resistor 28, the voltage drop U produced by the potential difference of the sensor is measured. Alternatively, by switching the two switches 30, 32, it is possible to determine the conductivity or the resistance of the sensor element by applying a voltage (DC or AC voltage) and by measuring the current flowing through. By arranging two evaluation units at one pair of electrodes 14, 16, it is consequently possible to compensate the moisture-dependency of the sensor signal.
  • In order to be able to absorb acidic gases—that is, gases such as carbon dioxide, nitrogen oxides or sulfur oxides which in contact with water result in an acidic solution—as quickly as possible and in sufficient quantity in polymer layer 26, the latter preferably contains a strong base such as tetraalkyl ammonium hydroxides or tetraalkyl ammonium hydrogen carbonates. These increase the solubility of the acidic gases in water that is bound in polymer layer 26 by removing the acid produced in the dissolving process.
  • For determining gases that react in a basic manner such as ammonia, an acid such as a sulphonic acid, for example, is preferably added to polymer layer 26. This promotes the solubility of basic gases in polymer layer 26. Moreover, polymer layer 26 may contain homogenization agents such as tensides for example.
  • For manufacturing sensor 10, an electrode paste preferably containing ceramic and metallic components, a so-called cermet, is applied onto substrate 12 and is sintered with the ceramic substrate 12. Polymer layer 26 is applied onto the electrode set-up in that a solution containing the polymer, a base or acid and other additives is deposited or imprinted and the solvent is removed. The polymer layer has a layer thickness of 10 to 100 μm, preferably between 20 and 40 μm.
  • Electrodes 14, 16 are contacted via circuit traces 22, 24, which are either formed also as cermet in one step together with electrodes 14, 16 or by imprinting a solution containing a hardenable resin and a precious-metal component and subsequent hardening of the solution. The use of a silver-containing epoxy resin is preferred.
  • The present invention is not limited to the exemplary embodiment described, but other specific embodiments in addition to the sensor described are conceivable as well.
  • Thus, for example, an activated carbon layer can be provided on polymer layer 26 to prevent the entry of gases that damage polymer layer 26 such as nitrogen oxides or sulfur oxides. Furthermore, a temperature measuring unit may be additionally provided for compensating temperature influences on the measured potential differences.

Claims (16)

1. A sensor for determining a concentration of a gas in a gas mixture, comprising:
a measuring electrode, the measuring electrode being a pH sensitive electrode;
a reference electrode; and
a polymer layer in contact with the gas mixture and the measuring electrode.
2. The sensor according to claim 1, wherein, in addition to measuring a pH value, a conductivity of the polymer layer is measured as well.
3. The sensor according to claim 1, wherein the measuring electrode contains an iridium oxide.
4. The sensor according to claim 1, wherein the measuring electrode is at least substantially shielded from the gas mixture by the polymer layer.
5. The sensor according to claim 1, wherein at least one of the measuring electrode and the reference electrode is an interdigital electrode.
6. The sensor according to claim 1, wherein the polymer layer includes a base.
7. The sensor according to claim 6, wherein the polymer layer contains a quaternary ammonium compound as the base.
8. The sensor according to claim 1, wherein the polymer layer contains an acid.
9. The sensor according to claim 8, wherein the polymer layer contains a sulphonic acid as the acid.
10. The sensor according to claim 1, wherein the polymer layer contains ethylcellulose.
11. The sensor according to claim 1, wherein the sensor is a sensitive element in a fire detector.
12. The sensor according to claim 1, wherein the sensor is a sensitive element in an air-quality sensor.
13. The sensor according to claim 1, wherein the sensor is a sensitive element for detecting ammonia.
14. A method for manufacturing a sensor for determining a concentration of a gas in a gas mixture having at least two electrodes that are deposited on a ceramic substrate and a polymer layer, the method comprising:
in a first step, producing the electrodes on the ceramic substrate by depositing an electrode paste and a subsequent heat treatment; and
in a second step, depositing the polymer layer by applying a polymer solution on at least one of the ceramic substrate and the electrodes and subsequently removing a solvent.
15. The method according to claim 14, wherein the polymer layer has a thickness of 10 to 50 μm.
16. The method according to claim 14, further comprising:
in a third step, contacting the electrodes by a hardenable, precious metal-containing polymer.
US11/000,387 2003-12-05 2004-11-30 Sensor for determining gases and method for manufacturing the sensor Abandoned US20050158457A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US12/418,150 US8758585B2 (en) 2003-12-05 2009-04-03 Sensor for determining gases and method for manufacturing the sensor

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE10356935A DE10356935A1 (en) 2003-12-05 2003-12-05 Sensor for the determination of gases and method for the production thereof
DE10356935.9 2003-12-05

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US12/418,150 Continuation US8758585B2 (en) 2003-12-05 2009-04-03 Sensor for determining gases and method for manufacturing the sensor

Publications (1)

Publication Number Publication Date
US20050158457A1 true US20050158457A1 (en) 2005-07-21

Family

ID=34625570

Family Applications (2)

Application Number Title Priority Date Filing Date
US11/000,387 Abandoned US20050158457A1 (en) 2003-12-05 2004-11-30 Sensor for determining gases and method for manufacturing the sensor
US12/418,150 Expired - Fee Related US8758585B2 (en) 2003-12-05 2009-04-03 Sensor for determining gases and method for manufacturing the sensor

Family Applications After (1)

Application Number Title Priority Date Filing Date
US12/418,150 Expired - Fee Related US8758585B2 (en) 2003-12-05 2009-04-03 Sensor for determining gases and method for manufacturing the sensor

Country Status (2)

Country Link
US (2) US20050158457A1 (en)
DE (1) DE10356935A1 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070080074A1 (en) * 2005-10-07 2007-04-12 Delphi Technologies, Inc. Multicell ammonia sensor and method of use thereof
WO2009103034A2 (en) * 2008-02-13 2009-08-20 Board Of Regents, The University Of Texas System System, method and apparatus for an amorphous iridium oxide film ph sensor

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI565944B (en) * 2015-12-11 2017-01-11 台灣奈米碳素股份有限公司 A gas sensor and manufacture method thereof

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4272328A (en) * 1979-12-05 1981-06-09 Eastman Kodak Company Buffer overcoat for CO2 ion-selective electrodes
US4900405A (en) * 1987-07-15 1990-02-13 Sri International Surface type microelectronic gas and vapor sensor
US5252292A (en) * 1989-05-18 1993-10-12 Mitsutoshi Hirata Ammonia sensor
US5720862A (en) * 1995-04-07 1998-02-24 Kyoto Daiichi Kagaku Co., Ltd. Sensor and production method of and measurement method using the same
US5958791A (en) * 1996-09-27 1999-09-28 Innovative Biotechnologies, Inc. Interdigitated electrode arrays for liposome-enhanced immunoassay and test device
US6241873B1 (en) * 1997-02-20 2001-06-05 Tdk Corporation Sold electrolytes, carbon dioxide sensors and method for correcting the output of sensors
US20040026267A1 (en) * 2002-02-28 2004-02-12 Thomas Brinz Sensor for determining gases and method of manufacturing same

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4952300A (en) * 1987-03-19 1990-08-28 Howard Diamond Multiparameter analytical electrode structure and method of measurement
EP0588153B1 (en) * 1992-09-14 1996-12-27 Siemens Aktiengesellschaft Gas sensor
US5322602A (en) * 1993-01-28 1994-06-21 Teledyne Industries, Inc. Gas sensors
US5573648A (en) * 1995-01-31 1996-11-12 Atwood Systems And Controls Gas sensor based on protonic conductive membranes
US5841021A (en) * 1995-09-05 1998-11-24 De Castro; Emory S. Solid state gas sensor and filter assembly
US5716506A (en) * 1995-10-06 1998-02-10 Board Of Trustees Of The University Of Illinois Electrochemical sensors for gas detection
US6682638B1 (en) * 1999-11-19 2004-01-27 Perkin Elmer Llc Film type solid polymer ionomer sensor and sensor cell

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4272328A (en) * 1979-12-05 1981-06-09 Eastman Kodak Company Buffer overcoat for CO2 ion-selective electrodes
US4900405A (en) * 1987-07-15 1990-02-13 Sri International Surface type microelectronic gas and vapor sensor
US5252292A (en) * 1989-05-18 1993-10-12 Mitsutoshi Hirata Ammonia sensor
US5720862A (en) * 1995-04-07 1998-02-24 Kyoto Daiichi Kagaku Co., Ltd. Sensor and production method of and measurement method using the same
US5958791A (en) * 1996-09-27 1999-09-28 Innovative Biotechnologies, Inc. Interdigitated electrode arrays for liposome-enhanced immunoassay and test device
US6241873B1 (en) * 1997-02-20 2001-06-05 Tdk Corporation Sold electrolytes, carbon dioxide sensors and method for correcting the output of sensors
US20040026267A1 (en) * 2002-02-28 2004-02-12 Thomas Brinz Sensor for determining gases and method of manufacturing same

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070080074A1 (en) * 2005-10-07 2007-04-12 Delphi Technologies, Inc. Multicell ammonia sensor and method of use thereof
WO2009103034A2 (en) * 2008-02-13 2009-08-20 Board Of Regents, The University Of Texas System System, method and apparatus for an amorphous iridium oxide film ph sensor
WO2009103034A3 (en) * 2008-02-13 2009-10-08 Board Of Regents, The University Of Texas System System, method and apparatus for an amorphous iridium oxide film ph sensor

Also Published As

Publication number Publication date
US20090205958A1 (en) 2009-08-20
DE10356935A1 (en) 2005-06-30
US8758585B2 (en) 2014-06-24

Similar Documents

Publication Publication Date Title
EP0293230B1 (en) Acidic gas sensors
Michalska et al. All solid-state hydrogen ion-selective electrode based on a conducting poly (pyrrole) solid contact
US5183549A (en) Multi-analyte sensing electrolytic cell
US7217354B2 (en) Method and apparatus for detection of chemical vapors
JP2005505778A (en) Ion-selective electrodes for direct organic drug analysis of saliva, sweat, and surface-wiping elements
CA2486501A1 (en) Ion exchange membranes and dissolved gas sensors
US20050034985A1 (en) Atmospheric corrosion sensor
US8758585B2 (en) Sensor for determining gases and method for manufacturing the sensor
JPH06508432A (en) Electrical analysis of liquids and detection elements used for it
US20070029196A1 (en) Reference electrode and detector using the same for detecting acidity or basicity of oil
US20040026267A1 (en) Sensor for determining gases and method of manufacturing same
WO1998011426A1 (en) Analytic cell
EP0805976B1 (en) Electrochemical planar metal/metal oxide electrode
Yun et al. Analysis of heavy-metal ions using mercury microelectrodes and a solid-state reference electrode on a Si wafer
US5908546A (en) Detection of hydrogen chloride
US20180266983A1 (en) Electrochemical sensor
Dybko et al. Miniaturized back-side contact transducer for potentiometric sensors
US7736478B2 (en) Ion solution concentration-detecting device
JP2813423B2 (en) Electrochemical gas sensor
JPH04364457A (en) Reagent developing and reagent fixing layer made of thick-film
KR100386304B1 (en) Potentiometric ammonia gas sensor and manufacturing process thereof
WO1992001219A1 (en) Ion-selective electrochemical sensor device
US20030087453A1 (en) Method and device for producing and screening composite arrangements
CA1311521C (en) Continuous electrochemical analyzer
GB2162997A (en) A fluoride ion sensitive field effect transistor

Legal Events

Date Code Title Description
AS Assignment

Owner name: ROBERT BOSCH GMBH, GERMANY

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:BRINZ, THOMAS;LEWIS, JANE;HEPPEL, CLAUS;REEL/FRAME:016413/0293;SIGNING DATES FROM 20050121 TO 20050124

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION