WO2000079262A1 - Vorrichtung zur messung von kohlenmonoxid - Google Patents
Vorrichtung zur messung von kohlenmonoxid Download PDFInfo
- Publication number
- WO2000079262A1 WO2000079262A1 PCT/EP2000/004084 EP0004084W WO0079262A1 WO 2000079262 A1 WO2000079262 A1 WO 2000079262A1 EP 0004084 W EP0004084 W EP 0004084W WO 0079262 A1 WO0079262 A1 WO 0079262A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- oxygen
- measuring
- sensor
- carbon monoxide
- containing atmosphere
- Prior art date
Links
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 title claims abstract description 33
- 229910002091 carbon monoxide Inorganic materials 0.000 title claims abstract description 33
- 239000001301 oxygen Substances 0.000 claims abstract description 60
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 60
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 58
- 239000007784 solid electrolyte Substances 0.000 claims description 21
- 239000003054 catalyst Substances 0.000 claims description 17
- 239000000463 material Substances 0.000 claims description 17
- 239000001257 hydrogen Substances 0.000 claims description 16
- 229910052739 hydrogen Inorganic materials 0.000 claims description 16
- 230000003647 oxidation Effects 0.000 claims description 13
- 238000007254 oxidation reaction Methods 0.000 claims description 13
- 238000005259 measurement Methods 0.000 claims description 11
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 10
- MCMNRKCIXSYSNV-UHFFFAOYSA-N ZrO2 Inorganic materials O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 claims description 7
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical group [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 claims description 7
- 229910052697 platinum Inorganic materials 0.000 claims description 4
- 229940056932 lead sulfide Drugs 0.000 claims description 3
- 229910052981 lead sulfide Inorganic materials 0.000 claims description 3
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 2
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 claims 1
- 229910001887 tin oxide Inorganic materials 0.000 claims 1
- 230000001590 oxidative effect Effects 0.000 abstract 1
- 239000007789 gas Substances 0.000 description 15
- 239000000523 sample Substances 0.000 description 12
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 10
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 6
- 239000000446 fuel Substances 0.000 description 5
- 150000002431 hydrogen Chemical class 0.000 description 5
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 4
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
- 230000004888 barrier function Effects 0.000 description 4
- 239000003570 air Substances 0.000 description 3
- 229910002092 carbon dioxide Inorganic materials 0.000 description 3
- 239000001569 carbon dioxide Substances 0.000 description 3
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 239000003792 electrolyte Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 238000012544 monitoring process Methods 0.000 description 2
- 229910052763 palladium Inorganic materials 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- 229910006404 SnO 2 Inorganic materials 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 239000012080 ambient air Substances 0.000 description 1
- 239000011260 aqueous acid Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- -1 oxygen ions Chemical class 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/0004—Gaseous mixtures, e.g. polluted air
- G01N33/0009—General constructional details of gas analysers, e.g. portable test equipment
- G01N33/0027—General constructional details of gas analysers, e.g. portable test equipment concerning the detector
- G01N33/0036—General constructional details of gas analysers, e.g. portable test equipment concerning the detector specially adapted to detect a particular component
- G01N33/004—CO or CO2
-
- 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
- G01N27/416—Systems
- G01N27/417—Systems using cells, i.e. more than one cell and probes with solid electrolytes
Definitions
- the present invention relates to a device for measuring carbon monoxide in an oxygen-containing atmosphere.
- electrochemical sensors for measuring carbon monoxide, hydrogen or hydrazine in the ambient air are known, which are suitable for detecting extremely low gas trace concentrations.
- Measuring cells in three-electrode arrangements are known for measuring carbon monoxide (cf. for example DE-OS 21 55 935).
- the known measuring cell consists of a measuring electrode, counter electrode and a reference electrode. With the help of an electronic potentiostat, the potential of the measuring electrode to the reference electrode is set and kept constant in the desired range. Herandiffundierende the carbon monoxide is oxidized at the measuring electrode, wherein an electric current is generated which is proportional "of the CO concentration.
- An electrochemical sensor is known from EP 0 047 898 A2 which comprises a catalytically active measuring electrode which is connected via an aqueous acid electrolyte to a non-polarizable air-oxygen electrode, an aqueous gel-like polymer adhesive being used as the electrolyte in which ionic substances are dissolved.
- the carbon monoxide passes through a diffusion barrier to the measuring electrode, where oxidation to carbon dioxide takes place.
- the oxygen present in the sensor's air space is converted to water at the counter electrode. induced.
- the air space is dimensioned such that the atmospheric oxygen consumed at the electrode causes only a slight change in the oxygen partial pressure in the air.
- an electrochemical high-temperature sensor for measuring motor vehicle exhaust gases is known, which is composed of a sensitive layer and an acoustic wave converter, the sensitive layer consisting of a semiconductor oxide layer such as Sn0 2 , Ti0 2 or Zr0 2 , which materials for CO and NOx are sensitive.
- H 2 reference electrode An electrochemical gas sensor with two electrically biased electrodes and an H 2 reference electrode is known from US Pat. No. 4,025,412.
- the H 2 reference electrode consists of a noble metal alloy and is connected to a perforated foil made of palladium, which has a high solubility for hydrogen. Molecular hydrogen generated on the reference electrode is absorbed by the palladium so that an essentially unchanged hydrogen atmosphere is maintained on the reference electrode, whereby the reference electrode is kept essentially at zero volts.
- a dynamic oxygen sensor (oxygen sensor MF010-O from Dittrich Elektronic GmbH and Co. KG, Baden-Baden), which consists of two zirconium dioxide disks covering a platinum ring on both sides, the cavity created by the covering of the platinum ring being a sealed one Measuring chamber for determining an oxygen partial pressure is used.
- one of the two zirconium dioxide disks is connected to a reversible current source and serves as an electrochemical oxygen pump which, depending on the polarity of the current source, can either pump oxygen into or out of the measuring chamber.
- the operation of the known oxygen sensor is as follows: When the power source is switched on, the measuring chamber is evacuated and the oxygen partial pressure in the chamber decreases linearly with the amount of charge transported, as a result of which the zirconium dioxide disk on the opposite side Nernst see tension rising. When the Nernst voltage reaches a predetermined value, the current direction applied to the first zirconium dioxide disk is reversed and oxygen ions are pumped into the chamber, whereupon the oxygen partial pressure rises and the Nernst voltage on the opposite disk decreases. After reaching a lower predetermined value for the Nernst 'see voltage, the current direction is changed again and the process is repeated periodically, the period time being linear to the oxygen partial pressure.
- An aluminum oxide layer is applied to the sensor, which catalyzes the combustion of combustible gases such as hydrogen, methane or carbon monoxide, since otherwise the presence of such combustible gases would lead to a reduction in the oxygen concentration on the outside of the sensor and thus to a falsification of the measurement.
- combustible gases such as hydrogen, methane or carbon monoxide
- the object of the invention is to provide a device for measuring carbon monoxide that is as compact as possible, simply constructed and inexpensive to manufacture.
- a device for measuring carbon monoxide in an oxygen-containing atmosphere is proposed with the features of claim 1.
- a measurement of carbon monoxide is carried out by measuring the concentration of oxygen in the oxygen-containing atmosphere using a first sensor (reference sensor) and measuring the oxygen concentration in parallel using a second sensor (measurement sensor) after m in the oxygen-containing atmosphere located carbon monoxide was oxidized.
- Oxygen is consumed by the oxidation of carbon monoxide to carbon dioxide, so that the measuring sensor measures a lower oxygen concentration than the reference sensor.
- the carbon monoxide concentration m of the oxygen-containing atmosphere can be derived from the difference between the two oxygen measurements with very high accuracy.
- the electrochemical sensors each measure the oxygen partial pressure.
- the electrochemical sensors are advantageously solid electrolyte sensors.
- the electrochemical sensors each have a sealed measuring chamber formed from a perforated layer of catalyst material and two solid electrolyte layers covering the layer. This allows a very simple and compact structure of a device according to the invention.
- the two electrochemical sensors have a common solid electrolyte layer as the basis, which allows particularly precise measurements to be carried out.
- the solid electrolyte is advantageously zirconium dioxide and the catalyst material is platinum.
- each electrochemical sensor is preceded by a prechamber shielded from hydrogen.
- the shielding of each antechamber is preferably formed by means of a material which catalyzes the oxidation of hydrogen, such as SnO 2 .
- the antechamber of the reference sensor has a material such as PbS that prevents the oxidation of carbon monoxide.
- the single figure shows a schematic representation of a cross section through an inventive device for measuring carbon monoxide.
- the device 10 shown in the figure for measuring carbon monoxide (hereinafter called CO probe for the sake of simplicity) comprises two electrochemical sensors, namely a reference sensor RS and a measuring sensor MS.
- the reference sensor RS is used to measure the concentration of oxygen in the oxygen-containing atmosphere, while the measuring sensor MS is used to oxidize carbon monoxide CO in the oxygen-containing atmosphere and the subsequent measurement of the remaining oxygen concentration.
- Each of the two electrochemical sensors RS, MS comprises a measuring chamber 20M, 20R, which is formed by a dense cavity between two disc-shaped solid electrolyte layers 16, 22R and 16, 22M, respectively, on both sides of a likewise disc-shaped layer 18 made of catalyst material with through bores are arranged to form the measuring chamber cavities 20M, 20R.
- the lower solid electrolyte layer of the two sensors MS, RS in the drawing is formed in one piece as a common, continuous base.
- the disk 18 made of catalyst material, which is also formed in one piece and has two through bores for forming the cavities for the measuring chambers 20M, 20R.
- a further ring 24M made of catalyst material is placed on the solid electrolyte disk 22M and is closed off at the top by a shield 14.
- the shield 14 consists of a material which catalyzes the oxidation of hydrogen H 2 , for example Sn0 2 .
- the cavity formed by the solid electrolyte disk 22M located below and the shield 14 located above from the bore of the catalyst ring 24M serves as a prechamber VM of the measuring probe.
- a ring 24R made of catalyst material is likewise placed on the solid electrolyte disk 22R, which ring is closed at the top by means of a shield 14, analogously to the measuring sensor MS.
- the antechamber VR of the reference sensor RS formed by the bore of the catalyst ring 24R comprises a “barrier layer” 26 made of a material that prevents the oxidation of CO, which is in particular PbS.
- the “barrier layer” 26 extends over and covers the bottom of the prechamber VR formed from the solid electrolyte of the disk 22R.
- the bottom of the CO probe 10, i.e. the surface of the solid electrolyte disk 16 lying below in the drawing is provided with a further catalyst layer 28 for oxygen catalysis.
- Zirconium dioxide is preferably used as the solid electrolyte and platinum as the catalyst material.
- the vertical walls of the CO probe 10 in the drawing are encapsulated with a layer 12 of glass.
- different gases reach the probe surface according to the arrows shown.
- the shielding 14 (zinc oxide filter) placed in front of the catalytically active surface of the two sensors MS, RS catalyzes an oxidation of the hydrogen H 2 in the oxygen-containing atmosphere to water H 2 0, while CO and 0 pass through the zinc oxide filter m the respective antechambers VM, VR of the two sensors MS, RS can reach.
- the barrier layer 26 made of lead sulfide PbS provided in the antechamber VR of the reference sensor RS maintains the catalytic activity of the platinum with respect to oxygen, so that it is transported further through the subsequent solid electrolyte layer m to the measuring chamber 20R of the reference sensor RS, whereas an oxidation of Carbon monoxide does not take place.
- the oxygen partial pressure of the oxygen-containing atmosphere is thus measured in the measuring chamber 20R of the reference sensor RS.
- the CO probe 10 is of course operated by applying a voltage source in a manner known to the person skilled in the art, which is not shown in more detail for reasons of clarity.
- the base of both sensors which serves as an electrode, is designed as a one-piece solid electrolyte disk 16, as already explained above.
- the one-piece base disk 16 arranged disk 18 made of catalyst material is grounded, and the Nernst 'see voltage is tapped on the solid electrolyte disks 22M or 22R which are in turn applied to the catalyst layer 18.
- the CO probe according to the invention can be designed to be very compact. Typical dimensions are a length of approx. 5 mm, a width of approx. 3 mm and a height of approx. 3 mm.
- the CO probe according to the present invention is particularly suitable for use in fuel cell systems.
- hydrogen-containing gas is generated from a raw fuel, carbon monoxide and carbon dioxide and optionally other constituents being additionally contained in the hydrogen-containing gas.
- the hydrogen-containing gas represents the aforementioned oxygen-containing atmosphere.
- the CO probe can be used here to measure the CO content of the hydrogen-containing gas.
- knowledge of the CO content in the hydrogen-rich gas is important, since in particular in so-called PEM fuel cells, the catalyst provided on the anode is poisoned by the carbon monoxide.
- the proportion of oxygen in the oxygen-containing atmosphere must be greater than the proportion of CO, since otherwise complete oxidation of the carbon monoxide would not be possible. Since fuel cell systems usually have a CO content in the range of 100 ppm, an oxygen content in the range of a few hundred ppm is sufficient for this application. In the event that there is no or insufficient oxygen in the gas to be examined, it is also possible to branch off a partial flow of the gas to be examined m into a measuring line and to add the gas to be examined before the CO sensor m arranged in the measuring line.
- the operating temperature of the CO probe according to the invention is approximately 500 ° C., which is achieved by means of a suitable heating. This heating can be, for example, a platm wire, which can also serve as a temperature sensor.
- the CO probe according to the present invention is also suitable for use in motor vehicles for measuring motor vehicle emissions.
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Analytical Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pathology (AREA)
- Immunology (AREA)
- Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- General Physics & Mathematics (AREA)
- Combustion & Propulsion (AREA)
- Medicinal Chemistry (AREA)
- Food Science & Technology (AREA)
- Molecular Biology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Measuring Oxygen Concentration In Cells (AREA)
Abstract
Description
Claims
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP00936720A EP1188053A1 (de) | 1999-06-19 | 2000-05-06 | Vorrichtung zur messung von kohlenmonoxid |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE1999128103 DE19928103A1 (de) | 1999-06-19 | 1999-06-19 | Vorrichtung zur Messung von Kohlenmonoxid |
DE19928103.3 | 1999-06-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2000079262A1 true WO2000079262A1 (de) | 2000-12-28 |
Family
ID=7911828
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2000/004084 WO2000079262A1 (de) | 1999-06-19 | 2000-05-06 | Vorrichtung zur messung von kohlenmonoxid |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP1188053A1 (de) |
DE (1) | DE19928103A1 (de) |
WO (1) | WO2000079262A1 (de) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10226207B4 (de) * | 2002-06-13 | 2017-08-03 | Volkswagen Ag | Verfahren und Vorrichtung zur Konzentrationsbestimmung einer Methankomponente |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5899747A (ja) * | 1981-12-09 | 1983-06-14 | Hitachi Ltd | ガス検知素子 |
US4441981A (en) * | 1978-05-10 | 1984-04-10 | Hitachi, Ltd. | Gas sensor |
WO1997013147A1 (en) * | 1995-09-29 | 1997-04-10 | Matsushita Electric Industrial Co., Ltd. | Gas sensor and manufacturing process thereof |
DE19610911A1 (de) * | 1996-03-20 | 1997-09-25 | Dittrich Elektronik J | Gassensor |
EP0872730A1 (de) * | 1997-04-16 | 1998-10-21 | Tokyo Gas Co., Ltd. | Festelektrolyt CO Sensor vom laminiertem Dickschichttyp |
-
1999
- 1999-06-19 DE DE1999128103 patent/DE19928103A1/de not_active Withdrawn
-
2000
- 2000-05-06 EP EP00936720A patent/EP1188053A1/de not_active Withdrawn
- 2000-05-06 WO PCT/EP2000/004084 patent/WO2000079262A1/de not_active Application Discontinuation
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4441981A (en) * | 1978-05-10 | 1984-04-10 | Hitachi, Ltd. | Gas sensor |
JPS5899747A (ja) * | 1981-12-09 | 1983-06-14 | Hitachi Ltd | ガス検知素子 |
WO1997013147A1 (en) * | 1995-09-29 | 1997-04-10 | Matsushita Electric Industrial Co., Ltd. | Gas sensor and manufacturing process thereof |
DE19610911A1 (de) * | 1996-03-20 | 1997-09-25 | Dittrich Elektronik J | Gassensor |
EP0872730A1 (de) * | 1997-04-16 | 1998-10-21 | Tokyo Gas Co., Ltd. | Festelektrolyt CO Sensor vom laminiertem Dickschichttyp |
Non-Patent Citations (1)
Title |
---|
PATENT ABSTRACTS OF JAPAN vol. 007, no. 202 (P - 221) 7 September 1983 (1983-09-07) * |
Also Published As
Publication number | Publication date |
---|---|
DE19928103A1 (de) | 2001-01-25 |
EP1188053A1 (de) | 2002-03-20 |
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