EP0852820A2 - Elektrodenmaterial für kohlenwasserstoffsensoren - Google Patents

Elektrodenmaterial für kohlenwasserstoffsensoren

Info

Publication number
EP0852820A2
EP0852820A2 EP96933384A EP96933384A EP0852820A2 EP 0852820 A2 EP0852820 A2 EP 0852820A2 EP 96933384 A EP96933384 A EP 96933384A EP 96933384 A EP96933384 A EP 96933384A EP 0852820 A2 EP0852820 A2 EP 0852820A2
Authority
EP
European Patent Office
Prior art keywords
electrode
electrode material
sensor
sensor according
material according
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.)
Withdrawn
Application number
EP96933384A
Other languages
German (de)
English (en)
French (fr)
Inventor
Ulrich Guth
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.)
Heraeus Electro Nite International NV
Original Assignee
Heraeus Electro Nite International NV
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
Priority claimed from DE19535381A external-priority patent/DE19535381A1/de
Priority claimed from DE19638181A external-priority patent/DE19638181A1/de
Application filed by Heraeus Electro Nite International NV filed Critical Heraeus Electro Nite International NV
Publication of EP0852820A2 publication Critical patent/EP0852820A2/de
Withdrawn legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/86Inert electrodes with catalytic activity, e.g. for fuel cells
    • H01M4/90Selection of catalytic material
    • H01M4/9016Oxides, hydroxides or oxygenated metallic salts
    • H01M4/9025Oxides specially used in fuel cell operating at high temperature, e.g. SOFC
    • H01M4/9033Complex oxides, optionally doped, of the type M1MeO3, M1 being an alkaline earth metal or a rare earth, Me being a metal, e.g. perovskites
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/01Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
    • C04B35/42Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on chromites
    • 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
    • G01N27/403Cells and electrode assemblies
    • G01N27/406Cells and probes with solid electrolytes
    • G01N27/407Cells and probes with solid electrolytes for investigating or analysing gases
    • G01N27/4075Composition or fabrication of the electrodes and coatings thereon, e.g. catalysts
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B1/00Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
    • H01B1/06Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances
    • H01B1/08Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances oxides
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/30Hydrogen technology
    • Y02E60/50Fuel cells

Definitions

  • the invention relates to a novel electrode material for hydrocarbon sensors and a novel sensor and a method for its production.
  • the concentration of unburned fuels in oxygen-containing gases can be determined in the combustion gas stream in m-situ by sensors, such as on a solid electrolyte, e.g. Yttrium stabilized Z ⁇ r ⁇ on ⁇ ox ⁇ d, two Elektro ⁇ en, which react in different ways to the sample gas.
  • the potential of one electrode is largely determined by the equilibrium oxygen partial pressure ⁇ es Gaeses, that of the other predominantly determined by the partial pressure of the fuel gas, so that a voltage can be measured between the electrons in the same gas, which depends on the hydrocarbon concentration depends.
  • Gold and alloys of gold and platinum are preferably used as CH-sensitive electrodes (e.g. A. Vogel, G. Baier, V. Fisch, Sensors and Actuators 15-16 (1993) 147-150).
  • the parameter z is either equal to 0 or is in the range from 0.01 to 0.29, from 0.3 to 0.6 or from 0.19 to 0.4.
  • Element A can be present with increasing z m of an oxidic phase next to the mixed oxide, so that the electrode is present as a whole m mixed phase.
  • the element o ⁇ er the element B mixture can also be heterogeneous as oxide neoen ⁇ em Mischoxi ⁇ present at a level of 0, 1 to 70. 5
  • a sensor according to the invention for combustible gases, in particular for hydrocarbons has a solid electrolyte and at least 2 electrodes, of which at least one electrode contains an electro material with the advantageous features described so far.
  • the second electrode has the same chemical composition as the first electrode.
  • a good sensitivity to fuel gas is then achieved by providing means for generating a temperature difference between the first and the second electrode.
  • the temperature difference between transition metal and B is at least a three- or two-valent redox-stable cation, an electrode with a perovskite structure for an electrochemical sensor can be created which, after sintering on a solid electrolyte or a ceramic carrier material, is stable for a long time even in an aggressive high-temperature environment.
  • fuel gas generally means gaseous and oxi ⁇ ieroare components under the operating conditions of the sensor
  • element or element mixture A and / or the element or element mixture has a germicidal catalytic activity .
  • msoeson ⁇ ere is advantageous if A em element or a mixture of elements from the group manganese, chromium, cobalt, iron, titanium.
  • the element or the element mixture B is preferably selected from the group consisting of gallium, aluminum, magnesium, calcium, gadolinium and other redox-stable rare earth elements.
  • A is manganese or chromium or a mixture or both and if an element or mixture of gallium, aluminum and magnesium.
  • An electrode material has been found to be particularly advantageous, where ⁇ is A and B is gallium.
  • Ln is a lanthanide or a mixture of lanthanides, especially lanthanum itself has particularly advantageous properties in the context of the present invention.
  • the parameter x is in the range from 0.001 to 3.99, in particular 0.1 to 0.9, preferably 0.1 to 0.8 or 0.2 to - 6 -
  • the carrier material can be a solid electrolyte, but it can also directly on an oxide ceramic carrier material, such as. B. AI2O3 can be printed and a solid electrolyte can be arranged above or next to it.
  • H 0 and / or organic solvents are advantageous as solvents, hydrophilic or organic solvents can be used.
  • a safe, complete oxidation of the electrode material is ensured if the reaction takes place in air or oxygen. If the reaction product forms a sinter cake, an additional annealing step can be carried out after comminuting the reaction product, in which the complete homogeneous reaction of the components is ensured.
  • the component Ln: 0 :. can also be a mineral such as cerite for industrial production. A composition which essentially corresponds to monazite is particularly advantageous.
  • a sensor according to the invention or a sensor which is produced according to the advantageous method can be used in particular as a hydrocarbon sensor for use in the exhaust gas of a combustion point, the combustion point being an internal combustion engine with internal or external combustion (in particular a gasoline engine or a diesel engine) or a heating system, such as an oil or natural gas heater.
  • the combustion point being an internal combustion engine with internal or external combustion (in particular a gasoline engine or a diesel engine) or a heating system, such as an oil or natural gas heater.
  • a good hydrocarbon sensitivity can be achieved if the solid electrolyte is from about 8 mole .- * Y: is made: 0 3 ZrO vollstabi ⁇ lêtem. By doping with Y ; 0 ; , empty spaces are generated in the partial oxygen lattice of the solid electrolyte.
  • the electrodes are placed on a solid electrolyte with a lower degree of doping at Y : 0 :. or the corresponding proportion of another cation with lower value the first and second electrodes are advantageously between 100 ° C and 200 ° C.
  • the second electrode is advantageously of the chemical composition Ln -, C y D0-, where Ln has already been explained above, C em is alkaline earth metal and D is at least trivalent transition metal. C is in particular strontium. D is advantageously manganese and / or chromium. Ln can be a different element or a different element mixture in the second electrode than in the first ⁇ lektro ⁇ e.
  • the parameter y is advantageously in the range 0.01 to 0.9, in particular 0.02 to 0.7, 0.05 to 0.5, 0.1 to 0.3 or 0.2
  • a method for producing a sensor for combustible gas using an electrode material according to the invention comprises the following steps:
  • Example 3 Printing and baking the paste on a carrier material.
  • the respective citrate or nitrate conversion of the starting materials can, for example, also be selected as the starting material.
  • the compound La 0 gosSrc.oosCrOs from the oxides L3 2 ÜJ H : 0, C ⁇ z0 2 and SrC0 3 is weighed in a stochiometric ratio and mixed 20 mm in a ball mill. The mixture is then converted into air in a aluminum oxide crucible at 1400 ° C. for 20 h. The sinter cake obtained is milled and annealed at 1650 ° C for 30 mm.
  • the electrode materials according to Example 1 and Example 2 can in a simple, electronics-compatible layer technology such as. B. screen printing on a solid electrolyte and then used in addition to a so-called equilibrium electrode, for example made of platinum.
  • the electrode material according to example 3 forms a mixed oxide of the perovskite type with negligible fuel gas sensitivity and can be used in addition to the electrodes according to example 1 and example 2 instead of the plate electrode.
  • the output signal of the sensor according to the invention is essentially dependent on the concentration of fuel gases in this exhaust gas, that is to say of hydrocarbons which have never been completely burnt or afterburned by the catalytic converter.
  • the oxides La : 0 were used to produce the compound LaCr - 0 Ga .0 . , H_0, Cr_0. and Ga_0 weighed in a stochiometric ratio and mixed 20 mm in a ball mill. The mixture is then reacted in a sintered corundum crucible at 1400 ° C. for 20 hours in air. The sinter cake obtained is milled and annealed at 1650 ° C for 30 mm. The complete formation of the desired product can be demonstrated with the aid of X-ray diffractometer images.
  • the oxides La 2 O-HO, Cr 0 and Al.O are weighed in a stochiometric ratio and mixed 20 mm in a ball mill and reacted in air at 1400 ° C. for 20 hours in a corundum crucible.
  • the sinter cake obtained is ground and subjected to an annealing process at 1650 ° C. for 30 mm in order to obtain the desired compound as pure as possible.
  • a sensor can be manufactured in which both electrodes are arranged on the same substrate, but a temperature gradient is set via the sensor, so that a temperature difference between the electrodes of 100 K to 150 K results. This temperature gradient can be generated in particular by a heating conductor printed on the carrier material of the sensor.
  • This embodiment has the advantage that both electrodes can be applied to the substrate or to the solid electrolytes in one production step.
  • the elements with the atomic numbers 57 to 71 are to be considered as lanthanides, the elements with the atomic numbers as trivalent transition metals. - 12 -
  • Electrode material according to one of the preceding claims characterized in that B em element or a mixture of elements from the group Ga, Al, Mg.
  • Electrode material according to one of the preceding claims characterized in that A is Cr.
  • electrode material according to one of the preceding claims, characterized in that B is Ga.
  • Electrode material according to one of the preceding claims, characterized in that Ln em element or a mixture of elements from the group La, Nd, Sm, Eu, Gd, Dy, Ho, Er, Tm, Yb or Lu.
  • Electrode material according to one of the preceding Ansprü ⁇ che, characterized in that Ln em element or a mixture of elements from the group of rare earth elements and alkaline earth metals.
  • Electrode material according to one of the preceding claims, characterized in that x is in the range from 0.001 to 0.99.
  • Electrode material according to one of the preceding claims characterized in that x is in the range from 0.01 to 0.9.
  • Electrode material according to one of the preceding claims characterized in that x is in the range from 0.1 to 0.8.
  • Electrode material according to one of the preceding claims characterized in that x is in the range from 0.2 to 0.5.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Ceramic Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Pathology (AREA)
  • Molecular Biology (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Physics & Mathematics (AREA)
  • Manufacturing & Machinery (AREA)
  • General Chemical & Material Sciences (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Measuring Oxygen Concentration In Cells (AREA)
  • Inert Electrodes (AREA)
EP96933384A 1995-09-25 1996-09-25 Elektrodenmaterial für kohlenwasserstoffsensoren Withdrawn EP0852820A2 (de)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
DE19535381 1995-09-25
DE19535381A DE19535381A1 (de) 1995-09-25 1995-09-25 Elektrodenmaterial für Kohlenwasserstoffsensoren
DE19638181 1996-09-18
DE19638181A DE19638181A1 (de) 1996-09-18 1996-09-18 Elektrodenmaterial für Kohlenwasserstoffsensoren
PCT/EP1996/004184 WO1997012413A2 (de) 1995-09-25 1996-09-25 Elektrodenmaterial für kohlenwasserstoffsensoren

Publications (1)

Publication Number Publication Date
EP0852820A2 true EP0852820A2 (de) 1998-07-15

Family

ID=26018861

Family Applications (1)

Application Number Title Priority Date Filing Date
EP96933384A Withdrawn EP0852820A2 (de) 1995-09-25 1996-09-25 Elektrodenmaterial für kohlenwasserstoffsensoren

Country Status (4)

Country Link
US (1) US6090249A (ja)
EP (1) EP0852820A2 (ja)
JP (1) JP2001513188A (ja)
WO (1) WO1997012413A2 (ja)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4241993B2 (ja) * 1999-04-01 2009-03-18 パナソニック株式会社 炭化水素センサ
JP5240432B2 (ja) * 2008-03-28 2013-07-17 国立大学法人九州大学 炭化水素濃度測定用センサ素子、および炭化水素濃度測定方法
FR2930075B1 (fr) * 2008-04-14 2011-03-18 Commissariat Energie Atomique Titanates de structure perovskite ou derivee et ses applications
US9006738B2 (en) * 2008-08-25 2015-04-14 Nxp, B.V. Reducing capacitive charging in electronic devices
JP5421267B2 (ja) * 2009-02-20 2014-02-19 日本特殊陶業株式会社 導電性酸化物焼結体、これを用いたサーミスタ素子、及びこれを用いた温度センサ
US20150274981A1 (en) * 2010-09-22 2015-10-01 Skyworks Solutions, Inc. Dual function lanthanide coatings

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3951603A (en) * 1972-07-08 1976-04-20 Hitachi, Ltd. Gas-sensor element and method for detecting reducing gas or oxygen gas
JPS5815731B2 (ja) * 1974-07-29 1983-03-28 株式会社日立製作所 ケムリ オヨビ ガスケンチソシ
JPS51150692A (en) * 1975-06-20 1976-12-24 Arita Kosei High conductivity composed substance
EP0006989B1 (en) * 1978-06-12 1983-06-15 Corning Glass Works Hot gas measuring device
DE2837118C2 (de) * 1978-08-25 1982-05-19 Dornier System Gmbh, 7990 Friedrichshafen Poröse Oxidelektroden für elektrochemische Hochtemperaturzellen
US4631238A (en) * 1985-01-18 1986-12-23 Westinghouse Electric Corp. Cobalt doped lanthanum chromite material suitable for high temperature use
US4562124A (en) * 1985-01-22 1985-12-31 Westinghouse Electric Corp. Air electrode material for high temperature electrochemical cells
US5306411A (en) * 1989-05-25 1994-04-26 The Standard Oil Company Solid multi-component membranes, electrochemical reactor components, electrochemical reactors and use of membranes, reactor components, and reactor for oxidation reactions
DE3723051A1 (de) * 1987-07-11 1989-01-19 Kernforschungsz Karlsruhe Halbleiter fuer einen resistiven gassensor mit hoher ansprechgeschwindigkeit
JPH0197848A (ja) * 1987-10-09 1989-04-17 Tech Res Assoc Conduct Inorg Compo 燃焼制御用センサ
US5128284A (en) * 1987-10-23 1992-07-07 Allied-Signal Inc. Preparation of lanthanum chromite powders by sol-gel
EP0411547A1 (en) * 1989-07-31 1991-02-06 Tonen Corporation Lanthanum chromite-based complex oxides and uses thereof
JP3141449B2 (ja) * 1990-11-05 2001-03-05 東陶機器株式会社 電極用ペロブスカイト型複合酸化物
JPH04269648A (ja) * 1991-02-26 1992-09-25 Toyota Central Res & Dev Lab Inc ガスセンサ
US5432024A (en) * 1992-10-14 1995-07-11 Ngk Insulators, Ltd. Porous lanthanum manganite sintered bodies and solid oxide fuel cells
DE4406276B4 (de) * 1993-02-26 2007-10-11 Kyocera Corp. Elektrisch leitendes Keramikmaterial
JPH0763719A (ja) * 1993-08-25 1995-03-10 Osaka Gas Co Ltd 酸素センサ

Non-Patent Citations (1)

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Title
See references of WO9712413A2 *

Also Published As

Publication number Publication date
US6090249A (en) 2000-07-18
WO1997012413A3 (de) 1997-06-19
WO1997012413A2 (de) 1997-04-03
JP2001513188A (ja) 2001-08-28

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