Classifications

• • G—PHYSICS
  • G01—MEASURING; TESTING
  • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
  • G01N27/00—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
  • G01N27/26—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
  • G01N27/403—Cells and electrode assemblies
  • G01N27/406—Cells and probes with solid electrolytes
  • G01N27/407—Cells and probes with solid electrolytes for investigating or analysing gases
  • G01N27/4075—Composition or fabrication of the electrodes and coatings thereon, e.g. catalysts

Definitions

• the invention relates to a layer system and a method for producing layer systems for gas sensors according to the preamble of the main claim.
• layer systems are known for example from DE-PS 28 52 647.
• EP-A 2-0373745 it is also known to protect the electrode layer of fuel cells or gas sensors against silicon and / or aluminum-containing compounds of the measuring gas by the fact that one or more oxides or compounds which form oxides when heated, of the metals from the group Ce, Sm, Mg, Be, Ca, Sr, Ti, Zr, Hf, Y, La, Ce, Pr, Nb, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb , Lu, Th, U, are applied.
• US Pat. No. 4,272,349 discloses the use of an outer protective layer made of Al 2 O 3 , which acts as a getter against catalyst poisons, in particular against phosphorus.
• the claimed layer system with the features of the main claim has the advantage that the mixed oxides the various pollutants commonly occurring in exhaust gas, such as. B. silicon, phosphorus, zinc or lead.
• the combination of alkali metals on the one hand and at least trivalent elements on the other hand results in mixed oxides, the reactivity and thermal stability of which can be adapted to the pollutants.
• the mixed oxide getters according to the invention react with the pollutants from the exhaust gas to form reaction products with high melting points above the maximum application temperature of the layer system.
• the high affinity of the alkali oxides for acidic oxides leads to a favorable getter effect against silicon and phosphorus.
• amphoteric or weakly acidic character of the at least trivalent mixed oxide partners also results in particular in the gettering action for divalent pollutants, such as lead or zinc.
• divalent pollutants such as lead or zinc.
• the invention thus enables a broader spectrum of pollutants to be covered.
• the mixed oxides by impregnation from a preferably aqueous solution, for example the nitrates or chlorides, or from solutions of organometallic compounds.
• a preferably aqueous solution for example the nitrates or chlorides, or from solutions of organometallic compounds.
• the compounds of the alkali metals and the trivalent or higher elements are selected so that they decompose at temperatures just above the application temperature of the sensor, the mixed oxides being formed in a very finely divided, highly reactive form.
• the impregnation process has the further advantage that, in addition to the mixed oxides, catalyst substances can also be introduced into the porous cover layer to adjust the sensor control position, in particular noble metal catalysts such as platinum, palladium, rhodium or the like.
• the mixed oxides are applied as additional layers to the finished sintered layer system solid electrolyte, electrode layer, porous cover layer or to the still unsintered layer system, which is then sintered together with this additional layer.
• the additional layer containing mixed oxide can be applied directly to the electrode layer, to the porous cover layer or as an intermediate layer between the porous cover layer and a further porous cover layer.
• the lithium aluminum oxide Li 2 O. Al 2 O 3
• particularly preferred mixed oxides containing lithium are: (2) Li 2 O. Ga 2 O 3
• Another preferred mixed oxide is sodium ⁇ -alumina
• Layer systems for exhaust gas sensors which determine the oxygen content can advantageously be produced by the method according to the invention.
• layer systems for other exhaust gas sensors can also be produced by the method, for example for CO, (NO) x or (CH) n sensors.
• the exhaust gas sensors produced after this are largely insensitive to pollutants from the exhaust gas.
• the starting point is a layer system according to DE-PS 28 52 647.
• the figure shows a layer system with a conventional solid electrolyte ceramic 10 made of zirconium dioxide fully or partially stabilized with yttrium, and a cermet electrode 11 made of 60 applied over it
• Layer 12 denotes a large number of pores whose diameter is in the range from 0.2 to 15 ⁇ m.
• the layer system is sintered in accordance with the information from DE-PS 28 52 647.
• the sintered layer system 10, 11, 12 described above is immersed in an equimolecular solution of LiNO 3 and Al (NO 3 ) 3 for three minutes at room temperature. The mixture is then drained for about 10 minutes. The porous cover layer 12 can be practically completely impregnated by capillary forces during the process.
• the layer system 10, 11, 12 is annealed in air at 1000 ° C. for two hours, so that the lithium aluminum mixed oxide can form in and on the porous cover layer 12 from the nitrates.
• the layer system modified in this way with mixed oxide can now be used to produce an exhaust gas sensor for oxygen, carbon monoxide, nitrogen oxides or hydrocarbons.

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• Chemical & Material Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• Health & Medical Sciences (AREA)
• Physics & Mathematics (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Electrochemistry (AREA)
• Molecular Biology (AREA)
• Analytical Chemistry (AREA)
• Biochemistry (AREA)
• General Health & Medical Sciences (AREA)
• General Physics & Mathematics (AREA)
• Immunology (AREA)
• Pathology (AREA)
• Measuring Oxygen Concentration In Cells (AREA)
• Investigating Or Analyzing Materials By The Use Of Fluid Adsorption Or Reactions (AREA)

Priority Applications (6)

Applications Claiming Priority (2)

Publications (1)

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ID=6416707

Family Applications (1)

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Citations (2)

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• 1990
  • 1990-10-20 DE DE4033388A patent/DE4033388C3/de not_active Expired - Fee Related
• 1991
  • 1991-09-21 BR BR919107029A patent/BR9107029A/pt not_active IP Right Cessation
  • 1991-09-21 US US08/039,059 patent/US5368713A/en not_active Expired - Lifetime
  • 1991-09-21 KR KR1019930700999A patent/KR100190208B1/ko not_active Expired - Fee Related
  • 1991-09-21 ES ES91916309T patent/ES2082227T3/es not_active Expired - Lifetime
  • 1991-09-21 DE DE59107046T patent/DE59107046D1/de not_active Expired - Lifetime
  • 1991-09-21 WO PCT/DE1991/000749 patent/WO1992007253A1/de not_active Ceased
  • 1991-09-21 JP JP03515437A patent/JP3105247B2/ja not_active Expired - Lifetime
  • 1991-09-21 EP EP91916309A patent/EP0553110B1/de not_active Expired - Lifetime

Patent Citations (2)

Non-Patent Citations (1)

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