US3578578A - Measuring means for measuring the exygen content in liquid and gaseous media - Google Patents

Measuring means for measuring the exygen content in liquid and gaseous media Download PDF

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US3578578A
US3578578A US763760A US3578578DA US3578578A US 3578578 A US3578578 A US 3578578A US 763760 A US763760 A US 763760A US 3578578D A US3578578D A US 3578578DA US 3578578 A US3578578 A US 3578578A
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measuring means
current collector
reference system
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measuring
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Otto Von Krusenstierna
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    • 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
    • G01N27/411Cells and probes with solid electrolytes for investigating or analysing of liquid metals
    • G01N27/4111Cells and probes with solid electrolytes for investigating or analysing of liquid metals using sensor elements of laminated structure

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  • the invention relates to the measurement of oxygen content of a liquid or gasseous material.
  • the prior art One method of determining the oxygen content in a medium is to measure the electromatoric force in an oxygen concentration element having a solid oxygen-ion conducting electrolyte, for example Ilime-stabilised zirconium dioxide.
  • the solid electrolyte of the measuring means normally consists of a relatively thick-walled tube provided with a bottom, on the inside of which is air or a mixture of a metal and its oxide.
  • a platinum Wire is often used as current collector.
  • the electrolyte is arranged only as a relatively thick-walled bottom While the cylindrical walls consist of an indifferent material.
  • the measuring means according to the invention permits measurement of the oxygen content in, for example, metal melts and exhause gases, with a maximum time delay of 3-5 seconds from the moment when the measuring means is inserted in the medium. This provides an essential improvement of the process control for, among other things, steel manufacture, casting and combustion.
  • the present invention relates to a measuring means for measuring the oxygen content in a liquid or gaseous medium, comprising a solid oxygen ion conducting electrolyte arranged in contact with a reference system having known oxygen potential and consisting of a metal and its oxide, which is ⁇ arranged in contact with a current collector, characterised in that the current collector is designed as a carrying element for the reference system and the electrolyte which are both arranged as layers on the current collector with the electrolyte outside the reference system.
  • the metal in the reference system may form a continuously coherent unit with the current collector which is then of the same metal and the metal exide may be arranged as a layer on the unit.
  • the surface layer of the body acting as current collector thus serves as the metal in the reference system.
  • the reference system may consist of a separate layer arranged on the current collector, which is then normally of a different metal from the metal in the current collector, and of a layer of the metal oxide arranged outside this layer, or consist of a layer of a mixture of the metal and the metal oxide.
  • the current collector is in the form of a wire or a rod having a thickness less than 5 mm. preferably less than 3 mm.
  • a particularly simple measuring means is obtained which is cheap to manufacture, especially in view of the fact that a wire or rod can be manufactured, for example, with layers of the reference system and electrolyte applied by plasma spraying, in great lengths which can then be cut into shorter lengths suitable for each measuring means to be manufactured from the wire or rod.
  • a current collector having wire or rod shape is used or some other shape, it is advantageous to use a thickness for the current collector less than 5 mm., preferably less than 3 mm., because the measuring means then has little thermal capacity.
  • the layer of the reference system may suitably have a thickness of 0.001-0.5, preferably 0.05-0.3 mm., and the electrolyte layer a thickness of (lOl-0 5 mm., preferably 0.05-0.3 mm.
  • the necessary counter-electrode may consist of a separate unit which is placed in the medium Whose oxygen content is to be determined. It may also be arranged together with the measuring means in a common casing or itself be shaped as a casing around part of the electrolyte layer of the measuring means.
  • the current collector may consist, for example, of one of the metals nickel, cobalt, iron, chromium, manganese, tungsten, molybdenum, niobium, tantalum or platinum.
  • the metal in the reference system may consist, for example, of one of the metals, nickel cobalt, iron, chromium, manganise, molybdenum, tungsten, niobium or tantalum.
  • suitable material in the electrolyte layer may be mentioned, amongst other things, lime-stabilised zirconium dioxide, which consists of ⁇ about mole percent Zr02 and about l5 mole percent CaO, or other oxygen ion conducting oxides such as yttrium-stabilised thorum oxide which consists of about 92.5 mole percent ThOg and about 7.5 mole percent Y2O3 and other substances described in Zeitschrift fr Chemie, March 1964, volume 3, pages 81-94.
  • lime-stabilised zirconium dioxide which consists of ⁇ about mole percent Zr02 and about l5 mole percent CaO
  • oxygen ion conducting oxides such as yttrium-stabilised thorum oxide which consists of about 92.5 mole percent ThOg and about 7.5 mole percent Y2O3 and other substances described in Zeitschrift fr Chemie, March 1964, volume 3, pages 81-94.
  • a suitable method of applying the layer of the reference system and the electrolyte is by means of plasma spraying or flame spraying them one after the other on the current collector. It is also possible to immerse the current collector first in a powder mixture of the metal of the reference system and the metal oxide (or only in the metal oxide if the current collector consists of the meta of the reference system) and then to sinter the product thus applied, after which the electrolyte is also applied by the same method in a second step.
  • An alternative method of applying the metal oxide on the current collector if this consists of the metal of the reference system is to oxidize the surface of the current collector so that it Abecomes coated with an oxide.
  • FIG. 1 shows schematically a measuring means according to the invention in which the current collector is of the same metal as the metal in the reference system and forms a continuously coherent unit with the metal in the reference system
  • FIG. 2 shows schematically a measuring means according to the invention in which the reference system consists of a mixture of a metal and its oxide,
  • FIG. 3 shows schematically a measuring means according to the invention which is built together with a counter electrode in an insulating casing
  • FIG. 4 shows schematically a measuring means according to the invention arranged together with a separate counter electrode in a space containing a liquid medium
  • FIG. 5 shows schematically a measuring means according to the invention, in which a counter electrode is arranged as a casing around a part of the electrolyte layer and which is arranged in a liquid medium,
  • FIG. 6 is a modification of the arrangement according to FIG. 5, and
  • FIG. 7 shows schematically a measuring means according to the invention arranged together with a coherent coutner-electrode in a space containing a gaseous medium.
  • the measuring means 1 consists rst of a nickel wire 2 having a diameter of 1 mm. and a length of cm. which, for example by being exposed to an oxygen-rich atmosphere, is oxidized on the surface thus forming a layer 3 of nickel oxide which may have a thickness of, for example, about 0.01 mm.
  • the nickel wire acts as current collector and at the same time forms part of the reference system, since the part of the surface layer of the nickel wire which faces the nickel oxide forms, together with the nickel oxide, the reference system of the measuring means.
  • the electrolyte layer consists of a 0.1 mm. thick layer 4 of particles of lime-stabilised zirconium dioxide sintered together and applied by plasma or llame spraying in a conventional manner.
  • the current collector of the Ineasf uring means 5 consists of a l mm. thick tungsten wire 6 on which is rst applied a reference system consisting of a layer 7 of particles of a mixture of chromium and chromium oxide (Cr203) sintered together and then a layer 8 of particles of lime-stabilised zirconium dioxide sintered together.
  • the layers 7 and 8 may both be applied by means of plasma spraying or ame spraying.
  • the lower end 11 of the measuring means is surrounded by the casing and the electrolyte layer 8 is instead exposed at a distance from said end by the arrangement of a window or opening 12 in the casing.
  • the embodiment according to FIG. 3 has advantages, particularly in cases Where the measuring means comprises a piece cut from a Wire having great length on which the reference system and the electrolyte have been applied. In such cases no reference system layer or electrolyte layer is obtained at the ends after cutting. The ends are protected by the casing 10.
  • the counter electrode 9 has an exposed end 13 which, like the electrolyte layer 8, cornes into contact with the oxygen-rich medium at the opening when the measuring means is being used.
  • the measuring means 5 according to FIG. 2, together with the counter electrode 14, is arranged in a vessel 1S with molten copper 16.
  • the size of the measuring means and the counter electrode is considerably exaggerated in relation to the size of the vessel.
  • the measuring means and the counter electrode are arranged in a common holder 17 and connected to a high-impedance voltmeter 18 to determine the oxygen content in the molten copper, or to a registering instrument.
  • the counter electrode 14 may consist, for example, of a molybdenum wire partly surrounded by a potective layer 19, for example of aluminium oxide.
  • the counter electrode is arranged as a tubular casing 20, 21, respectively, around a part of the electrolyte layer of the measuring means. At the same time the casing provides a protection for the electrolyte layer of the measuring means.
  • the measuring means and the counter electrode are arranged in a melt of steel 22 in the Vessel 23.
  • the measuring means and the counter electrode are connected to a Voltmeter 18. They may also be connected to a registering instrument or to a means regulating the supply of components to the melt to inuence its oxygen content.
  • the lower part 24 of the measuring means is exposed to be in contact with the melt.
  • FIG. 5 the arrangement according to FIG.
  • the casing tube 20 may consist of tungsten or of a metal ceramic material such as a mixture of molybdenum and aluminum oxide.
  • the wall thickness may be, for example, 2 mm.
  • the measuring means 1 according to FIG. l together with the counter electrode 27 joined to this, is arranged in a drum 28 for exhaust gases.
  • the measuring means and counter electrode are insulated from the drum by the insulation 29 and connected to the voltmeter 18 to determine the oxygen content in the exhaust gases. They may also be connected to a registering instrument or to a means influencing valves in conduits for the supply of fuel and air to the space where the combustion takes place.
  • the counter electrode 27 which is in electron-conducting contact with the electrolyte layer may, for example, consist of platinum in the form of a coherent net or a layer with open pores.
  • Measuring means for measuring the oxygen content in a liquid or gaseous medium comprising a current collector, a solid oxygen ion conducting eyectrolyte having an exposed surface and a reference system having known oxygen potential and consisting essentially of a metal and its oxide, in which the current collector constitutes a carrying element for the reference system and the electrolyte which are both arranged as layers on and around the current collector with the reference system in contact with and secured to the current collector and the electrolyte outside and in contact with and secured to the reference system, said current collector comprising a solid wire or rod having a thickness of less than 5 mm, said reference system layer having a thickness of 0.001-0.5 mm., and said electrolyte layer having a thickness of G01-0.5mm.
  • Measuring means in which the metal in the reference system forms a continuous coherent unit with the current collector which is of the same metal and that the metal oxide is arranged as a layer on the unit.
  • Measuring means in which the reference system comprises a separate layer of the metal arranged on the current collector and a layer of metal oxide or a layer of a mixture of the metal and the metal oxide arranged on the current collector.
  • Measuring means in which a protective casing is arranged around a part of the electrolyte layer.
  • Measuring means according to claim 4 in which the protective casing is electrically conducting and constitutes a counter-electrode.
  • the metal of the reference system consists essentially of a metal of the group consisting of nickel, cobalt, iron, chromium manganese, molybdenum, tungsten, niobium and tantalum.
  • VMeasurisg means according to claim 1, in which the current collector and the metal in the reference system consist essentially of nickel.
  • Measuring means according to claim 1 in which the current collector consists essentially of tungsten and the metal in the reference system consists essentially of chromium.

Abstract

MEASURING MEANS FOR MEASURING THE EXYGEN CONTENT IN A LIQUID OR GASEOUS MEDIUM, COMPRISIG A SOLID OXYGEN ION CONDUCTING ELECTROLYTE ARRANGED IN CONTACT WITH A REFERENCE SYSTEM HAVING KNOWN OXYGEN POTENTIAL AND CONSISTING OF A METAL AND ITS OXIDE WHICH IS ARRANGED IN CONTACT WITH A CURRENT COLLECTOR. THE CURRENT COLLECTOR IS

DESIGNED AS A CARRYING ELEMENT FOR THE REFERENCE SYSTEM AND THE ELECTROLYTE WHICH ARE BOTH ARRANGED AS LAYERS ON THE CURRENT COLLECTOR WITH THE ELECTROLYTE OUTSIDE THE REFERENCE SYSTEM.

Description

Ml? 1191971 o. voN kRusENsTlERNA l MEASURING MEANS FOR MEASURING THE OXYGEN CONTENT IN LIQUIDy AND eAsEous MEDIA Filed sept. so, 1968 Fig. /`V Fig. 2 Fz'g NI/ENTORA OTT O VON KRUSE NSTIEPNA BY M 6 .Q F w m,
United States Patent 3,578,578 MEASURING MEANS FOR MEASURING THE OXYGEN CONTENT IN LIQUID AND GASEOUS MEDIA Otto Von Krusenstierna, Vasteras, Sweden, assigner to Allmnna Svenska Elektriska Aktiebolaget, Vasteras, Sweden Filed Sept. 30, 1968, Ser. No. 763,760 Claims priority, application Sweden, Sept. 28, 1967, 13,306/67 Int. Cl. G01n 27/46 ILS. Cl. 204-195 10 Claims ABSTRACT F THE DISCLOSURE Measuring means for measuring the exygen content in a liquid or gaseous medium, comprising a solid oxygen ion conducting electrolyte arranged in contact with a reference system having known oxygen potential and consisting of a metal and its oxide which is arranged in contact with a current collector. The current collector is designed as a carrying element for the reference system and the electrolyte which are both arranged as layers on the current collector with the electrolyte outside the reference system.
BACKGROUND OF THE INVENTION (l) Field of the invention The invention relates to the measurement of oxygen content of a liquid or gasseous material.
In the manufacture of steel and when casting steel knowledge of the oxygen content of the steel during the process is of great importance. This is also the case in the manufacture and casting of many metals, for example copper, and many alloys other than steel. With combustion reactions for heating purposes it is often of great importance to be able to determine the oxygen content of the exhaust gases so that the combustion can be regulated for optimum exploitation of the fuel. Thus, in processes of various types, there is a need to be able to eiectively determine the oxygen content in a liquid or gaseous medium.
(2) The prior art One method of determining the oxygen content in a medium is to measure the electromatoric force in an oxygen concentration element having a solid oxygen-ion conducting electrolyte, for example Ilime-stabilised zirconium dioxide. In previously known means the solid electrolyte of the measuring means normally consists of a relatively thick-walled tube provided with a bottom, on the inside of which is air or a mixture of a metal and its oxide. A platinum Wire is often used as current collector. During measuring the outside of the tube is arranged in contact with the medium Whose oxygen content is to be measured. In a similar alternative arrangement, also known, the electrolyte is arranged only as a relatively thick-walled bottom While the cylindrical walls consist of an indifferent material.
SUMMARY OF THE INVENTION According to the present invention it has proved possible to effect a measuring means with which equilibrium is reached in a considerably shorter time than with those described above. The measuring means according to the invention permits measurement of the oxygen content in, for example, metal melts and exhause gases, with a maximum time delay of 3-5 seconds from the moment when the measuring means is inserted in the medium. This provides an essential improvement of the process control for, among other things, steel manufacture, casting and combustion.
The present invention relates to a measuring means for measuring the oxygen content in a liquid or gaseous medium, comprising a solid oxygen ion conducting electrolyte arranged in contact with a reference system having known oxygen potential and consisting of a metal and its oxide, which is `arranged in contact with a current collector, characterised in that the current collector is designed as a carrying element for the reference system and the electrolyte which are both arranged as layers on the current collector with the electrolyte outside the reference system.
According to one embodiment of the invention the metal in the reference system may form a continuously coherent unit with the current collector which is then of the same metal and the metal exide may be arranged as a layer on the unit. The surface layer of the body acting as current collector thus serves as the metal in the reference system. According to another embodiment the reference system may consist of a separate layer arranged on the current collector, which is then normally of a different metal from the metal in the current collector, and of a layer of the metal oxide arranged outside this layer, or consist of a layer of a mixture of the metal and the metal oxide.
According to a particularly preferred embodiment of the invention the current collector is in the form of a wire or a rod having a thickness less than 5 mm. preferably less than 3 mm. When a current collector in wire or rod form is used a particularly simple measuring means is obtained which is cheap to manufacture, especially in view of the fact that a wire or rod can be manufactured, for example, with layers of the reference system and electrolyte applied by plasma spraying, in great lengths which can then be cut into shorter lengths suitable for each measuring means to be manufactured from the wire or rod. Whether a current collector having wire or rod shape is used or some other shape, it is advantageous to use a thickness for the current collector less than 5 mm., preferably less than 3 mm., because the measuring means then has little thermal capacity. The layer of the reference system may suitably have a thickness of 0.001-0.5, preferably 0.05-0.3 mm., and the electrolyte layer a thickness of (lOl-0 5 mm., preferably 0.05-0.3 mm.
The necessary counter-electrode may consist of a separate unit which is placed in the medium Whose oxygen content is to be determined. It may also be arranged together with the measuring means in a common casing or itself be shaped as a casing around part of the electrolyte layer of the measuring means.
The current collector may consist, for example, of one of the metals nickel, cobalt, iron, chromium, manganese, tungsten, molybdenum, niobium, tantalum or platinum.
The metal in the reference system may consist, for example, of one of the metals, nickel cobalt, iron, chromium, manganise, molybdenum, tungsten, niobium or tantalum.
As an example of suitable material in the electrolyte layer may be mentioned, amongst other things, lime-stabilised zirconium dioxide, which consists of `about mole percent Zr02 and about l5 mole percent CaO, or other oxygen ion conducting oxides such as yttrium-stabilised thorum oxide which consists of about 92.5 mole percent ThOg and about 7.5 mole percent Y2O3 and other substances described in Zeitschrift fr Chemie, March 1964, volume 3, pages 81-94.
A suitable method of applying the layer of the reference system and the electrolyte is by means of plasma spraying or flame spraying them one after the other on the current collector. It is also possible to immerse the current collector first in a powder mixture of the metal of the reference system and the metal oxide (or only in the metal oxide if the current collector consists of the meta of the reference system) and then to sinter the product thus applied, after which the electrolyte is also applied by the same method in a second step. An alternative method of applying the metal oxide on the current collector if this consists of the metal of the reference system is to oxidize the surface of the current collector so that it Abecomes coated with an oxide.
BRIEF DESCRIPTION OF THE DRAWINGS The invention will be further explained by describing a number of embodiments with reference to the accompanying drawing in which FIG. 1 shows schematically a measuring means according to the invention in which the current collector is of the same metal as the metal in the reference system and forms a continuously coherent unit with the metal in the reference system,
FIG. 2 shows schematically a measuring means according to the invention in which the reference system consists of a mixture of a metal and its oxide,
FIG. 3 shows schematically a measuring means according to the invention which is built together with a counter electrode in an insulating casing,
FIG. 4 shows schematically a measuring means according to the invention arranged together with a separate counter electrode in a space containing a liquid medium,
FIG. 5 shows schematically a measuring means according to the invention, in which a counter electrode is arranged as a casing around a part of the electrolyte layer and which is arranged in a liquid medium,
FIG. 6 is a modification of the arrangement according to FIG. 5, and
FIG. 7 shows schematically a measuring means according to the invention arranged together with a coherent coutner-electrode in a space containing a gaseous medium.
DESCRIPTION OF THE PREFERRED EMBODIMENTS The measuring means 1 according to FIG. 1 consists rst of a nickel wire 2 having a diameter of 1 mm. and a length of cm. which, for example by being exposed to an oxygen-rich atmosphere, is oxidized on the surface thus forming a layer 3 of nickel oxide which may have a thickness of, for example, about 0.01 mm. The nickel wire acts as current collector and at the same time forms part of the reference system, since the part of the surface layer of the nickel wire which faces the nickel oxide forms, together with the nickel oxide, the reference system of the measuring means. The electrolyte layer consists of a 0.1 mm. thick layer 4 of particles of lime-stabilised zirconium dioxide sintered together and applied by plasma or llame spraying in a conventional manner.
According to FIG. 2 the current collector of the Ineasf uring means 5 consists of a l mm. thick tungsten wire 6 on which is rst applied a reference system consisting of a layer 7 of particles of a mixture of chromium and chromium oxide (Cr203) sintered together and then a layer 8 of particles of lime-stabilised zirconium dioxide sintered together. The layers 7 and 8 may both be applied by means of plasma spraying or ame spraying.
According to FIG. 3 the measuring means 5 according to FIG. 2 together with the counter electrode 9, for example a tungsten wire, is arranged in a tubular casing 10 of aluminium oxide or some other heat-resistant insulating material. The lower end 11 of the measuring means is surrounded by the casing and the electrolyte layer 8 is instead exposed at a distance from said end by the arrangement of a window or opening 12 in the casing. The embodiment according to FIG. 3 has advantages, particularly in cases Where the measuring means comprises a piece cut from a Wire having great length on which the reference system and the electrolyte have been applied. In such cases no reference system layer or electrolyte layer is obtained at the ends after cutting. The ends are protected by the casing 10. The counter electrode 9 has an exposed end 13 which, like the electrolyte layer 8, cornes into contact with the oxygen-rich medium at the opening when the measuring means is being used.
According to FIG. 4 the measuring means 5 according to FIG. 2, together with the counter electrode 14, is arranged in a vessel 1S with molten copper 16. As in FIGS. 5-7 the size of the measuring means and the counter electrode is considerably exaggerated in relation to the size of the vessel. The measuring means and the counter electrode are arranged in a common holder 17 and connected to a high-impedance voltmeter 18 to determine the oxygen content in the molten copper, or to a registering instrument.
The counter electrode 14 may consist, for example, of a molybdenum wire partly surrounded by a potective layer 19, for example of aluminium oxide.
In the arrangements accoding to FIGS. 5 and 6 the counter electrode is arranged as a tubular casing 20, 21, respectively, around a part of the electrolyte layer of the measuring means. At the same time the casing provides a protection for the electrolyte layer of the measuring means. The measuring means and the counter electrode are arranged in a melt of steel 22 in the Vessel 23. As in the arrangement according to FIG. 4 the measuring means and the counter electrode are connected to a Voltmeter 18. They may also be connected to a registering instrument or to a means regulating the supply of components to the melt to inuence its oxygen content. In the arrangement according to FIG. 5 the lower part 24 of the measuring means is exposed to be in contact with the melt. In the arrangement according to FIG. 6 said lower part is surrounded by the casing tube 21 and the electrolyte layer 8 is instead exposed at a ditsance from the outer end 25 of the measuring means by the arranegment of a window or opening 26 in the casing tube 21. The embodiment of the measuring means according to FIG. 6 has the same advantages as those mentioned previously for the arrangement to FIG. 3. If the outer end is exposed before the casing tube is positioned, another insulation from the casing tube can be applied to the outer ends if necessary. In the case exemplied, for example, the casing tube 20, 21, respectively, may consist of tungsten or of a metal ceramic material such as a mixture of molybdenum and aluminum oxide. The wall thickness may be, for example, 2 mm.
According to FIG. 7 the measuring means 1 according to FIG. l, together with the counter electrode 27 joined to this, is arranged in a drum 28 for exhaust gases. The measuring means and counter electrode are insulated from the drum by the insulation 29 and connected to the voltmeter 18 to determine the oxygen content in the exhaust gases. They may also be connected to a registering instrument or to a means influencing valves in conduits for the supply of fuel and air to the space where the combustion takes place. The counter electrode 27 which is in electron-conducting contact with the electrolyte layer may, for example, consist of platinum in the form of a coherent net or a layer with open pores.
I claim:
1. Measuring means for measuring the oxygen content in a liquid or gaseous medium, comprising a current collector, a solid oxygen ion conducting eyectrolyte having an exposed surface and a reference system having known oxygen potential and consisting essentially of a metal and its oxide, in which the current collector constitutes a carrying element for the reference system and the electrolyte which are both arranged as layers on and around the current collector with the reference system in contact with and secured to the current collector and the electrolyte outside and in contact with and secured to the reference system, said current collector comprising a solid wire or rod having a thickness of less than 5 mm, said reference system layer having a thickness of 0.001-0.5 mm., and said electrolyte layer having a thickness of G01-0.5mm.
2. Measuring means according to claim 1, in which the metal in the reference system forms a continuous coherent unit with the current collector which is of the same metal and that the metal oxide is arranged as a layer on the unit.
3. Measuring means according to claim 1, in which the reference system comprises a separate layer of the metal arranged on the current collector and a layer of metal oxide or a layer of a mixture of the metal and the metal oxide arranged on the current collector.
4. Measuring means according to claim 1, in which a protective casing is arranged around a part of the electrolyte layer.
5. Measuring means according to claim 4, in which the protective casing is electrically conducting and constitutes a counter-electrode.
6. Measuring means according to claim 1, in which the electrolyte layer consists essentially of lime-stabilized zirconium dioxide.
7. Measuring means according to claim 1, in which the metal of the reference system consists essentially of a metal of the group consisting of nickel, cobalt, iron, chromium manganese, molybdenum, tungsten, niobium and tantalum.
l8. Measuring means according to claim 1, in which the current collector consists essentially of a metal of the group consisting of nickel, cobalt, iron, chromium, manganese, molybdenum, tungsten, niobium and tantalum.
9. VMeasurisg means according to claim 1, in which the current collector and the metal in the reference system consist essentially of nickel.
10. Measuring means according to claim 1, in which the current collector consists essentially of tungsten and the metal in the reference system consists essentially of chromium.
References Cited UNITED STATES PATENTS 3,300,344 1/1967 Bray et al. 136-86 3,401,062 9/1968 Lyons 136-86 3,403,090 9/ 1968 Tajiri et al. 204-195 3,460,991 8/ 1969 White 136-86 3,464,861 9/ 1969 Williams et al. 136-86 TA-HSUNG TUNG, Primary Examiner U.S. Cl. X.R.
US763760A 1967-09-28 1968-09-30 Measuring means for measuring the exygen content in liquid and gaseous media Expired - Lifetime US3578578A (en)

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US3768259A (en) * 1971-07-06 1973-10-30 Universal Oil Prod Co Control for an engine system
US3793155A (en) * 1969-12-22 1974-02-19 Little Inc A Apparatus for monitoring the oxygen content of a molten metal
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US4021326A (en) * 1972-06-02 1977-05-03 Robert Bosch G.M.B.H. Electro-chemical sensor
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US4174258A (en) * 1978-05-03 1979-11-13 Bendix Autolite Corporation Solid electrolyte oxygen sensor with zero oxygen reference
DE2833397A1 (en) * 1978-07-29 1980-02-14 Ferrotron Elektronik Gmbh Measuring cell with probe - has reference substance separated from melt by solid electrolyte and includes thermocouple
US4208265A (en) * 1977-11-11 1980-06-17 Toyota Jidosha Kogyo Kabushiki Kaisha Oxygen sensor element and process of manufacture
EP0024192A1 (en) * 1979-08-13 1981-02-25 EASTMAN KODAK COMPANY (a New Jersey corporation) Silver/silver halide electrodes and process for preparing same
DE2934244A1 (en) 1979-08-24 1981-03-12 Ferrotron Elektronik Gmbh Determn. of temp. and oxygen activity of melts, esp. steel - via measuring cell contg. thermocouple and comparator substance with known oxygen activity
US4313799A (en) * 1980-04-04 1982-02-02 Owens-Corning Fiberglas Corporation Oxygen sensor and method for determining the oxygen activity in molten glass
US4354912A (en) * 1979-02-03 1982-10-19 Robert Bosch Gmbh Solid electrochemical sensor
US4406754A (en) * 1980-03-28 1983-09-27 Kabushiki Kaisha Kobe Seiko Sho Method and probe for the rapid determination of sulfur level
US4636292A (en) * 1984-05-03 1987-01-13 Ab Asea-Atom Electrode for electrochemical measurements in aqueous solutions of high temperatures
US4828673A (en) * 1987-03-09 1989-05-09 Yokogawa Electric Corporation Apparatus for measuring combustible gas concentration in flue gas
DE2954228C2 (en) * 1979-08-24 1989-06-22 Fischer, Wilhelm Anton, Prof. Dr.-Ing.Habil.
US5332449A (en) * 1991-10-28 1994-07-26 Heraeus Electro-Nite International N.V. Immersion sensor for molten metals
US5480523A (en) * 1992-03-24 1996-01-02 Pilkington Plc Method of using oxygen measuring probe
US5792329A (en) * 1995-04-12 1998-08-11 Heraeus Electro-Nite International, N.V. Apparatus to measure an electro-chemical activity
DE10310387B3 (en) * 2003-03-07 2004-07-22 Heraeus Electro-Nite International N.V. Measurement sensor determining oxygen activity and other elements in molten metal or slag, includes solid electrolyte tube coated with calcium zirconate and a fluoride
DE102004022763B3 (en) * 2004-05-05 2005-09-15 Heraeus Electro-Nite International N.V. Device for determining the oxygen activity in metal or slag melts, useful for measuring the content of silicon and carbon, includes solid electrolyte coated with layer of zirconium silicate and a fluoride
US20060096861A1 (en) * 2002-11-26 2006-05-11 Wilhelm Merkens Probe for determination of oxygen activity in metal melts and methods for its production
US20100018348A1 (en) * 2007-01-22 2010-01-28 Heraeus Electro-Nite International N.V. Method for Influencing the Properties of Cast Iron, and Oxygen Sensor
DE102012002027A1 (en) 2012-02-03 2013-08-08 Heraeus Electro-Nite International N.V. Measuring device used to determine e.g. sulfur in slag melt e.g. iron melt, comprises measuring head placed at end of support tube on which electrochemical cell is arranged, where cell includes solid electrolyte tube including coating

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DE2819381C2 (en) * 1978-05-03 1982-08-19 Ferrotron Elektronik Gmbh, 4030 Ratingen Solid electrolyte cell for correction-free measurement of low oxygen activities in molten steel
JPS6034062B2 (en) * 1979-05-25 1985-08-06 日産自動車株式会社 Air fuel ratio detection device
JPS564047A (en) * 1979-06-26 1981-01-16 Nissan Motor Co Ltd Lamination type membrane-covered oxygen sensor
JPS6034064B2 (en) * 1979-12-18 1985-08-06 日産自動車株式会社 Stacked membrane structure oxygen sensor
HU191839B (en) * 1983-05-16 1987-04-28 Nehezipari Mueszaki Egyetem Method and device for measuring continuously the solute alumina content of cryolite melts with alumina content during operation
JPS6283641A (en) * 1985-10-08 1987-04-17 Sharp Corp Sensor element
DE102006005476A1 (en) * 2006-01-26 2007-09-13 Heraeus Electro-Nite International N.V. Apparatus for determining a characteristic of a molten metal or a slag layer resting on the molten metal

Cited By (40)

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US3793155A (en) * 1969-12-22 1974-02-19 Little Inc A Apparatus for monitoring the oxygen content of a molten metal
US3652427A (en) * 1969-12-22 1972-03-28 Little Inc A Method for monitoring the oxygen and carbon contents in a molten metal
US3711394A (en) * 1970-10-29 1973-01-16 Atomic Energy Commission Continuous oxygen monitoring of liquid metals
US3768259A (en) * 1971-07-06 1973-10-30 Universal Oil Prod Co Control for an engine system
US4021326A (en) * 1972-06-02 1977-05-03 Robert Bosch G.M.B.H. Electro-chemical sensor
US3915830A (en) * 1974-06-12 1975-10-28 Westinghouse Electric Corp Solid electrolyte electrochemical cell with self contained reference
US4035244A (en) * 1974-11-01 1977-07-12 Mita Industrial Company Limited Electric recording process
US4040929A (en) * 1975-09-15 1977-08-09 Universal Oil Products Company Oxygen sensor having thin film electrolyte
US4126532A (en) * 1976-09-22 1978-11-21 Nissan Motor Company, Limited Oxygen sensor
US4076608A (en) * 1976-11-04 1978-02-28 Nissan Motor Company, Limited Oxygen sensor
US4208265A (en) * 1977-11-11 1980-06-17 Toyota Jidosha Kogyo Kabushiki Kaisha Oxygen sensor element and process of manufacture
FR2422951A1 (en) * 1977-12-24 1979-11-09 Max Planck Inst Eisenforschung IMMERSION PROBE
US4174258A (en) * 1978-05-03 1979-11-13 Bendix Autolite Corporation Solid electrolyte oxygen sensor with zero oxygen reference
DE2833397A1 (en) * 1978-07-29 1980-02-14 Ferrotron Elektronik Gmbh Measuring cell with probe - has reference substance separated from melt by solid electrolyte and includes thermocouple
US4354912A (en) * 1979-02-03 1982-10-19 Robert Bosch Gmbh Solid electrochemical sensor
EP0024192A1 (en) * 1979-08-13 1981-02-25 EASTMAN KODAK COMPANY (a New Jersey corporation) Silver/silver halide electrodes and process for preparing same
DE2934244A1 (en) 1979-08-24 1981-03-12 Ferrotron Elektronik Gmbh Determn. of temp. and oxygen activity of melts, esp. steel - via measuring cell contg. thermocouple and comparator substance with known oxygen activity
DE2954228C2 (en) * 1979-08-24 1989-06-22 Fischer, Wilhelm Anton, Prof. Dr.-Ing.Habil.
US4406754A (en) * 1980-03-28 1983-09-27 Kabushiki Kaisha Kobe Seiko Sho Method and probe for the rapid determination of sulfur level
US4313799A (en) * 1980-04-04 1982-02-02 Owens-Corning Fiberglas Corporation Oxygen sensor and method for determining the oxygen activity in molten glass
US4636292A (en) * 1984-05-03 1987-01-13 Ab Asea-Atom Electrode for electrochemical measurements in aqueous solutions of high temperatures
US4828673A (en) * 1987-03-09 1989-05-09 Yokogawa Electric Corporation Apparatus for measuring combustible gas concentration in flue gas
US5332449A (en) * 1991-10-28 1994-07-26 Heraeus Electro-Nite International N.V. Immersion sensor for molten metals
US5480523A (en) * 1992-03-24 1996-01-02 Pilkington Plc Method of using oxygen measuring probe
US5611901A (en) * 1992-03-24 1997-03-18 Pilkington Plc Oxygen measuring probe
US5792329A (en) * 1995-04-12 1998-08-11 Heraeus Electro-Nite International, N.V. Apparatus to measure an electro-chemical activity
US20060096861A1 (en) * 2002-11-26 2006-05-11 Wilhelm Merkens Probe for determination of oxygen activity in metal melts and methods for its production
US7578913B2 (en) 2002-11-26 2009-08-25 Specialty Minerals (Michigan) Inc. Probe for determination of oxygen activity in metal melts and methods for its production
DE10310387B3 (en) * 2003-03-07 2004-07-22 Heraeus Electro-Nite International N.V. Measurement sensor determining oxygen activity and other elements in molten metal or slag, includes solid electrolyte tube coated with calcium zirconate and a fluoride
US7141151B2 (en) * 2003-03-07 2006-11-28 Heraeus Electro-Nite International N.V. Measurement device for determining oxygen activity in molten metal or slag
US20040173473A1 (en) * 2003-03-07 2004-09-09 Heraeus Electro-Nite International N.V. Measurement device for determining oxygen activity in molten metal or slag
EP1593963A1 (en) 2004-05-05 2005-11-09 Heraeus Electro-Nite International N.V. Measurement set-up to determine the oxygen activity in metallic or slag melts
US20050247575A1 (en) * 2004-05-05 2005-11-10 Heraeus Electro-Nite International N.V. Measurement device for determining oxygen activity in metal or slag melts
DE102004022763B3 (en) * 2004-05-05 2005-09-15 Heraeus Electro-Nite International N.V. Device for determining the oxygen activity in metal or slag melts, useful for measuring the content of silicon and carbon, includes solid electrolyte coated with layer of zirconium silicate and a fluoride
US7169274B2 (en) 2004-05-05 2007-01-30 Heraeus Electro-Nite International N.V. Measurement device for determining oxygen activity in metal or slag melts
US20100018348A1 (en) * 2007-01-22 2010-01-28 Heraeus Electro-Nite International N.V. Method for Influencing the Properties of Cast Iron, and Oxygen Sensor
CN102944601A (en) * 2007-01-22 2013-02-27 贺利氏电子耐特国际股份公司 Sensor for measuring the oxygen content in cast iron
US8449741B2 (en) 2007-01-22 2013-05-28 Heraeus Electro-Nite International N.V. Method for influencing the properties of cast iron, and oxygen sensor
US8557176B2 (en) 2007-01-22 2013-10-15 Heraeus Electro-Nite International N.V. Method for influencing the properties of cast iron
DE102012002027A1 (en) 2012-02-03 2013-08-08 Heraeus Electro-Nite International N.V. Measuring device used to determine e.g. sulfur in slag melt e.g. iron melt, comprises measuring head placed at end of support tube on which electrochemical cell is arranged, where cell includes solid electrolyte tube including coating

Also Published As

Publication number Publication date
SE322927B (en) 1970-04-20
FR1582347A (en) 1969-09-26
DE1798307C3 (en) 1973-09-20
GB1232487A (en) 1971-05-19
DE1798307B2 (en) 1973-03-01
DE1798307A1 (en) 1972-02-24

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