US3480397A - Gas analysis method for determining the oxygen content of a gas containing carbon dioxide - Google Patents

Gas analysis method for determining the oxygen content of a gas containing carbon dioxide Download PDF

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US3480397A
US3480397A US490215A US3480397DA US3480397A US 3480397 A US3480397 A US 3480397A US 490215 A US490215 A US 490215A US 3480397D A US3480397D A US 3480397DA US 3480397 A US3480397 A US 3480397A
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gas
filament
oxygen content
measuring
carbon dioxide
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US490215A
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Frank A Baumgartel
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Elsag Bailey Inc
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Bailey Meter Co
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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
    • G01N27/02Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance
    • G01N27/04Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance by investigating resistance
    • G01N27/14Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance by investigating resistance of an electrically-heated body in dependence upon change of temperature
    • G01N27/16Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance by investigating resistance of an electrically-heated body in dependence upon change of temperature caused by burning or catalytic oxidation of surrounding material to be tested, e.g. of gas
    • 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T436/00Chemistry: analytical and immunological testing
    • Y10T436/20Oxygen containing
    • Y10T436/207497Molecular oxygen
    • Y10T436/208339Fuel/air mixture or exhaust gas analysis

Definitions

  • This invention relates to improvements in the detection and measurement of the oxygen content of a gas.
  • this invention relates to the method of measuring the oxygen content of a gas and eliminating the effect of the endothermic reactions, thermal conductivity effects and effects of specific heat.
  • the catalytic combustion method for analysis of oxygen in a gaseous mixture employs the combining of a gas sample with a standardized fuel, such as hydrogen.
  • a gas sample such as hydrogen.
  • the fuel and oxygen bearing gas are exposed to the heated filament where it burns and raises the filament temperature.
  • This method works very well and is accurate unless carbon dioxide (CO is present, then an error is introduced.
  • CO carbon dioxide
  • the CO error was due only to the thermal conductivity of the CO
  • Still another object of my invention is to provide a method for determining the oxygen content of a gas by measuring the change in current required to maintain the filament at a constant temperature.
  • I show schematically a Wheatstone bridge measuring circuit including a heated filament and a control circuit for maintaining said filament at a constant temperature.
  • I show a platinum measuring filament 1 enclosed within a chamber 2, shown schematically, through which the oxygen bearing gas and fuel are passed at a constant rate of flow.
  • the measuring filament 1 comprises one leg of a Wheatstone bridge 3 supplied by a direct current source 4, shown as a battery. Current flowing from the source 4 through the measuring filamentl raises its temperature to a point where exposing the filament to an oxygen-fuel mixture causes said mixture to burn.
  • the Wheatstone bridge 3 also consists of two calibrating resistors 6 and 7 and a dropping resistor 8. Through proper selection of the calibrating resistors 6 and 7 the bridge output voltage between terminals 9 and 11 will be zero when the measuring filament 1 is at the desired operating temperature.
  • a circular chart recorder 12 Connected across the dropping resistor 8 and responsive to the voltage drop developed across said resistor is a circular chart recorder 12.
  • Various circular chart or strip chart recorders can 'be used to record the voltage drop across the resistor 8, the operation of these recorders is well known and no description is deemed necessary.
  • Certain adjustment circuits would be required in the recorder to calibrate the full scale deflection of the recording pen to coincide with the range of voltages developed across the resistor 8 as the oxygen content of the gas varied from zero percent to maximum.
  • the Wheatstone bridge 3 is unbalanced and a voltage difference exists between terminals 9 and 11.
  • a differential amplifier 13 Connected to the bridge terminal 9 is one input of a differential amplifier 13; connected to the bridge terminal 11, through a bias supply 14, shown as a battery, is the second input of the differential amplifier 13.
  • the differential amplifier 13 is well understood, in my circuit it amplifies the voltage difference between the bridge terminals 9 and 11 and generates, at its output terminal, a voltage inversely proportional thereto.
  • I connect the first stage of a two-stage emitter-follower amplifier to the output of the differential amplifier 13 and the second stage in series with the power supply 4.
  • the first emitter-follower stage consists of a transistor 15 having a base electrode B connected to the output of the differential amplifier 13 and a collector electrode C connected to the negative side of the power supply 4. Also connected to the base electrode B of the first stage transistor 15 is a capacitor 16.
  • a bias resistor 17 interconnects the emitter electrode E of the first stage transistor 15 and the base electrode B of the second stage transistor 18 to the positive terminal of the power supply 4.
  • the second stage transistor 18 controls current flow from the power supply 4 through the Wheatstone bridge 3. Connected to the negative side of the power supply 4 is the collector electrode C of the second stage transistor 18, the emitter electrode E of this transistor connects to the junction of the filament 1 and the calibrating resistor 6.
  • the system heretofore described is only one of many that can be used to carry out the objects of my invention.
  • the important feature of my invention is to maintain the filament temperature at a constant value to eliminate the errors produced by various reactions and CO and H thermal conductivity effects.
  • the measuring filament 1 must be operated at a temperature between 700 F. and 800 F.
  • the system I have shown and described maintains a correct temperature 'by controlling the current flow through the collector-emitter junction of the second stage transistor 18.
  • the Wheatstone bridge 3 In operation of the circuit, initially the Wheatstone bridge 3 must be balanced using a gas having zero percent oxygen content (a calibrating procedure). The calibrating resistors 6 and 7 are adjusted until the temperature of the filament is between 700 F. and 800 F. and the bridge output is zero. Exposing the measuring filament 1 to an oxygen bearing gas by passing the gas through the chamber 2 causes said gas to burn thereby increasing the filament temperature and changing its resistance. The ratios of the bridge arms are no longer equal and a voltage difference develops between the bridge terminals 9 and 11. A signal inversely proportional to the bridge unbalance between terminals 9 and 11 will be generated at the output of the differential amplifier 13 thus lowering the base drive voltage connected to the first stage transistor 15.
  • the second stage transistor base drive voltage With the base electrode B of the second stage transistor 18 connected to the emitter electrode E of transistor 15 the second stage transistor base drive voltage will likewise be lowered. Reducing the base drive voltage to the second stage transistor 18 reduces its collector-emitter current flow thus lowering the current fiow through the measuring filament 1. Reducing the current flow through the filament 1 lowers its temperature and its resistance value. This operation continues until the bridge ratios are again equal and the voltage difference between terminals 9 and 11 is zero.
  • the voltage drop across the resistor 8 is a measure of oxygen content.
  • the recorder 12 responds to the voltage drop across the resistor 8 thus indicating and recording the oxygen content of the gas.
  • a method of determining the oxygen content of a gas containing carbon dioxide (CO comprising:
  • a combustible mixture exposing a heated catalytic measuring filament in one 5 leg of a Wheatstone bridge to the gas-hydrogen mix- References Cited UNITED STATES PATENTS ture being analyzed thereby causing catalytic corn- 2 219 540 10/1940 Miner 23 232 bustion of said mixture; measuring the unbalance voltage across said Wheatstone bridge caused by the catalytic combustion of 10 2449485 9/1948 8 2232 23:255 gas'fuel f 2,698,223 12/1954 Richardson 23 2s5 generating a control signal proportional to the magnitude 9 Said Imbalance slgnal; and JOSEPH SCOVRONEK, Primary Examiner controlling the current flow through said measuring filament as a function of the magnitude and polarity 15 US. Cl. X.R.

Description

Nov. 25, 1969 F. A. BAUMGARTEL 3,430,397
GAS ANALYSIS METHOD FOR DETERMINING THE OXYGEN CONTENT OF A GAS CONTAINING CARBON DIOXIDE Filed Sept. 27, 1965 INVENTOR. FRANK A. BAUNIGARTEL A TTORNEY United States Patent 3,480,397 GAS ANALYSIS METHOD FOR DETERMINING THE OXYGEN CONTENT OF A GAS CONTAIN ING CARBON DIOXIDE Frank A. Baumgartel, Mentor, Ohio, assignor to Bailey Meter Company, a corporation of Delaware Filed Sept. 27, 1965, Ser. No. 490,215 Int. Cl. G01n 27/62 US. Cl. 23-232 5 Claims ABSTRACT OF THE DISCLOSURE A method for determining the oxygen content of a gas containing carbon dioxide (CO by maintaining a heated filament at a constant temperature between 700 F. and 800 F. to minimize the effect of the endothermic H +CO =CO+H O reaction, the CO and H 0 thermal conductivity effect and the specific heat effect.
This invention relates to improvements in the detection and measurement of the oxygen content of a gas. In particular this invention relates to the method of measuring the oxygen content of a gas and eliminating the effect of the endothermic reactions, thermal conductivity effects and effects of specific heat.
It has long been recognized that the presence of carbon dioxide (CO introduces an error when measuring the oxygen content of a gas by means of catalytic combustion around a heated platinum filament. In the past this error was simply ignored on the basis that it was small and insignificant. Now, however, with the need for greater accuracies in the measurement of oxygen content, this error cannot be ignored.
One of the most common and widely accepted methods of gas constituent measurement in use today is by means of catalytic combustion around a heated filament. Usually the filament is made of platinum and connected as one leg of a Wheatstone bridge circuit. The bridge current heats the platinum filament to the level necessary for catalytic combustion of the gas. Combustion of the gas raises the filament temperature and consequently its resistance. The amount of heat generated by the gas burning is directly related to its oxygen content. Thus, the filament resistance varies as the oxygen content of the gas being measured. With the filament as one leg of a Wheatstone bridge the change of filament resistance causes the bridge to be unbalanced; the magnitude of the unbalance is a measure of oxygen content.
The catalytic combustion method for analysis of oxygen in a gaseous mixture employs the combining of a gas sample with a standardized fuel, such as hydrogen. The fuel and oxygen bearing gas are exposed to the heated filament where it burns and raises the filament temperature. This method works very well and is accurate unless carbon dioxide (CO is present, then an error is introduced. Formerly, it was believed this error was due only to the thermal conductivity of the CO Now, however, it has been proven that the CO error is due to the combined effect of the specific heat and thermal conductivity of the CO the endothermic conductivity of CO tends to increase the catalyst temperature as does the thermal conductivity of H 0; the endo- "ice thermic H +CO =CO+H O reaction and the specific heat tend to lower the catalyst temperature. When there is an excessive amount of hydrogen available the reaction CO +4H =CH +2H O also introduces an error due to the presence of methane.
It is an object of my invention to provide a method for eliminating the CO effect when measuring the oxygen content of a gas.
Another object of my invention is to provide a method for measuring the oxygen content of a gas wherein I maintain the filament at a constant temperature to eliminate the effect of the endothermic H +CO =CO+H O reaction, the CO and H 0 thermal conductivity effect and the specific heat effects.
Still another object of my invention is to provide a method for determining the oxygen content of a gas by measuring the change in current required to maintain the filament at a constant temperature.
Another object of my invention is to provide a method for determining the oxygen content of a gas by maintaining a heated platinum filament at a constant temperature between 700 F. and 800 F. to minimize the effect of the endothermic H +CO =CO+H O reaction, the CO and H 0 thermal conductivity effect and the specific heat effect.
These and various other objects of my invention will be particularly pointed out in the appended claims and will be apparent from the following description taken in conjunction with the drawing.
Referring to the drawing, I show schematically a Wheatstone bridge measuring circuit including a heated filament and a control circuit for maintaining said filament at a constant temperature.
In particular, I show a platinum measuring filament 1 enclosed within a chamber 2, shown schematically, through which the oxygen bearing gas and fuel are passed at a constant rate of flow. For a description of the general operation of analyzers of this design, reference is made to United States Patent No. 2,420,430 issued to C. Johnson. The measuring filament 1 comprises one leg of a Wheatstone bridge 3 supplied by a direct current source 4, shown as a battery. Current flowing from the source 4 through the measuring filamentl raises its temperature to a point where exposing the filament to an oxygen-fuel mixture causes said mixture to burn.
The Wheatstone bridge 3 also consists of two calibrating resistors 6 and 7 and a dropping resistor 8. Through proper selection of the calibrating resistors 6 and 7 the bridge output voltage between terminals 9 and 11 will be zero when the measuring filament 1 is at the desired operating temperature. Connected across the dropping resistor 8 and responsive to the voltage drop developed across said resistor is a circular chart recorder 12. Various circular chart or strip chart recorders can 'be used to record the voltage drop across the resistor 8, the operation of these recorders is well known and no description is deemed necessary. Certain adjustment circuits would be required in the recorder to calibrate the full scale deflection of the recording pen to coincide with the range of voltages developed across the resistor 8 as the oxygen content of the gas varied from zero percent to maximum.
Exposing the measuring filament 1 to an oxygen bearing gas causes catalytic combustion to take place thereby raising the filament temperature and its resistance. As a result, the Wheatstone bridge 3 is unbalanced and a voltage difference exists between terminals 9 and 11. Connected to the bridge terminal 9 is one input of a differential amplifier 13; connected to the bridge terminal 11, through a bias supply 14, shown as a battery, is the second input of the differential amplifier 13. Operationally, the differential amplifier 13 is well understood, in my circuit it amplifies the voltage difference between the bridge terminals 9 and 11 and generates, at its output terminal, a voltage inversely proportional thereto.
To maintain the temperature of the measuring filament 1 at the desired predetermined level, in accordance with the objects of my invention, I connect the first stage of a two-stage emitter-follower amplifier to the output of the differential amplifier 13 and the second stage in series with the power supply 4. The first emitter-follower stage consists of a transistor 15 having a base electrode B connected to the output of the differential amplifier 13 and a collector electrode C connected to the negative side of the power supply 4. Also connected to the base electrode B of the first stage transistor 15 is a capacitor 16. A bias resistor 17 interconnects the emitter electrode E of the first stage transistor 15 and the base electrode B of the second stage transistor 18 to the positive terminal of the power supply 4. The second stage transistor 18 controls current flow from the power supply 4 through the Wheatstone bridge 3. Connected to the negative side of the power supply 4 is the collector electrode C of the second stage transistor 18, the emitter electrode E of this transistor connects to the junction of the filament 1 and the calibrating resistor 6.
It should be obvious to those skilled in the art that the system heretofore described is only one of many that can be used to carry out the objects of my invention. As I have emphasized, the important feature of my invention is to maintain the filament temperature at a constant value to eliminate the errors produced by various reactions and CO and H thermal conductivity effects. To minimize the various endothermic reactions, thermal conductivity effects and specific heat effects, the measuring filament 1 must be operated at a temperature between 700 F. and 800 F. The system I have shown and described maintains a correct temperature 'by controlling the current flow through the collector-emitter junction of the second stage transistor 18.
In operation of the circuit, initially the Wheatstone bridge 3 must be balanced using a gas having zero percent oxygen content (a calibrating procedure). The calibrating resistors 6 and 7 are adjusted until the temperature of the filament is between 700 F. and 800 F. and the bridge output is zero. Exposing the measuring filament 1 to an oxygen bearing gas by passing the gas through the chamber 2 causes said gas to burn thereby increasing the filament temperature and changing its resistance. The ratios of the bridge arms are no longer equal and a voltage difference develops between the bridge terminals 9 and 11. A signal inversely proportional to the bridge unbalance between terminals 9 and 11 will be generated at the output of the differential amplifier 13 thus lowering the base drive voltage connected to the first stage transistor 15.
With the base electrode B of the second stage transistor 18 connected to the emitter electrode E of transistor 15 the second stage transistor base drive voltage will likewise be lowered. Reducing the base drive voltage to the second stage transistor 18 reduces its collector-emitter current flow thus lowering the current fiow through the measuring filament 1. Reducing the current flow through the filament 1 lowers its temperature and its resistance value. This operation continues until the bridge ratios are again equal and the voltage difference between terminals 9 and 11 is zero.
Since the current flow through the filament 1 and the dropping resistor 8 varies inversely with the oxygen content of the gas, the voltage drop across the resistor 8 is a measure of oxygen content. The recorder 12 responds to the voltage drop across the resistor 8 thus indicating and recording the oxygen content of the gas.
In accordance with the patent statutes, I have described my invention in terms of a preferred embodiment. The invention may be practiced otherwise than as described and still 'be within the scope of the appended claims.
What I claim as new and desire to secure by Letters Patent of the United States is:
1. A method of determining the oxygen content of a gas containing carbon dioxide (CO comprising:
mixing the gas to be analyzed with hydrogen to produce a combustible mixture;
exposing a heated catalytic measuring means in one leg of a Wheatstone bridge to said combustible mixture;
burning said combustible mixture in the presence of said measuring means;
measuring the unbalance voltage across said Wheatstone bridge caused by the catalytic combustion of said combustible mixture; and
maintaining said measuring means at a constant temperature between 700 F. and 800 F. to minimize the effect of the reaction CO +4H =CH +2H O, the H 0 thermal conductivity effect and the CO thermal conductivity and specific heat effects.
2. A method for determining the oxygen content of a gas-fuel mixture containing carbon dioxide (CO said method minimizing the effect of the endothermic H +CO =CO+H O reaction, the H 0 thermal conductivity and CO thermal conductivity and specific heat effects comprising:
mixing the gas to be analyzed with hydrogen to produce a combustible mixture;
exposing a heated catalytic measuring filament in one leg of a Wheatstone bridge to the gas-hydrogen mixture thereby causing catalytic combustion of said mixture;
measuring the unbalance voltage across said Wheatstone bridge caused by the catalytic combustion of said gas-fuel mixture; and
adjusting the power source supplying said Wheatstone bridge in response to said unbalance voltage to maintain the measuring filament temperature between 700 F and 800 F. thereby minimizing the effect of the H +CO =CO+H O endothermic reaction, the H O thermal conductivity and CO thermal conductivity and specific heat effects.
3. A method for determining the oxygen content of a gas-fuel mixture containing carbon dioxide (CO said method minimizing the effect of the endothermic H +CO =CO+H 0 reaction, the H 0 thermal conductivity and the CO thermal conductivity and specific heat effects, comprising:
mixing the gas to be analyzed with hydrogen to produce a combustible mixture;
passing the gas-hydrogen mixture over a heated catalytic measuring filament at a constant rate of flow, said filament comprising one leg of a Wheatstone bridge; burning the gas-hydrogen mixture in the presence of said filament thereby generating a voltage across said bridge; and adjusting the power source supplying said Wheatstone bridge in response to said bridge output to maintain the measuring filament temperature between 700 F. and 800 F. thereby minimizing the effect of the endothermic H +CO =CO+H O reaction, the H 0 thermal conductivity and the CO thermal conductivity and specific heat effects.
4. The method of claim 3 including measuring the current flow through said filament to determine the oxygen content of the gas-fuel mixture containing carbon dioxide.
5. A method for determining the oxygen content of a gas-fuel mixture containing carbon dioxide (CO said method minimizing the effect of the endothermic H +CO =CO+H O reaction, the H 0 thermal con- 5 6 ductivity and CO thermal conductivity and specific heat between 700 F. and 800 F. thereby minimizing the effects, comprising: effect of the endothermic reaction and the thermal mixing the gas to be analyzed with hydrogen to produce conductivity and specific heat eifects.
a combustible mixture; exposing a heated catalytic measuring filament in one 5 leg of a Wheatstone bridge to the gas-hydrogen mix- References Cited UNITED STATES PATENTS ture being analyzed thereby causing catalytic corn- 2 219 540 10/1940 Miner 23 232 bustion of said mixture; measuring the unbalance voltage across said Wheatstone bridge caused by the catalytic combustion of 10 2449485 9/1948 8 2232 23:255 gas'fuel f 2,698,223 12/1954 Richardson 23 2s5 generating a control signal proportional to the magnitude 9 Said Imbalance slgnal; and JOSEPH SCOVRONEK, Primary Examiner controlling the current flow through said measuring filament as a function of the magnitude and polarity 15 US. Cl. X.R.
of said control signal to maintain its temperature 23-255; 7327
US490215A 1965-09-27 1965-09-27 Gas analysis method for determining the oxygen content of a gas containing carbon dioxide Expired - Lifetime US3480397A (en)

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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3683671A (en) * 1970-09-14 1972-08-15 Univ Kansas State Measuring system including thermal conductivity detector means
US3864959A (en) * 1971-12-16 1975-02-11 Pye Ltd Thermal conductivity detector apparatus
US4741198A (en) * 1986-10-06 1988-05-03 Beckman Industrial Corporation Thermal conductivity detector assembly
US4835108A (en) * 1986-07-28 1989-05-30 The Babcock & Wilcox Company Method for measuring free oxygen in a combustible atmosphere
US5297419A (en) * 1992-07-16 1994-03-29 Thermco Instrument Corporation Linearizing gas analyzer
US20130133403A1 (en) * 2009-11-25 2013-05-30 Siemens Aktiengesellschaft Method and Arrangement for Gas Chromatographic Analysis of a Gas Sample

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8918280D0 (en) * 1989-08-10 1989-09-20 Neotronics Technology Plc Combustible gas monitors

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2219540A (en) * 1939-01-25 1940-10-29 Power Patents Co Gas analysis method and apparatus
US2404993A (en) * 1940-01-22 1946-07-30 Cities Service Oil Co Gas analyzer
US2420430A (en) * 1943-05-26 1947-05-13 Bailey Meter Co Gas analyzer
US2449485A (en) * 1942-01-01 1948-09-14 Bailey Meter Co Gas analyzer
US2698223A (en) * 1947-05-02 1954-12-28 Cambridge Instr Co Inc Gas analyzer

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2219540A (en) * 1939-01-25 1940-10-29 Power Patents Co Gas analysis method and apparatus
US2404993A (en) * 1940-01-22 1946-07-30 Cities Service Oil Co Gas analyzer
US2449485A (en) * 1942-01-01 1948-09-14 Bailey Meter Co Gas analyzer
US2420430A (en) * 1943-05-26 1947-05-13 Bailey Meter Co Gas analyzer
US2698223A (en) * 1947-05-02 1954-12-28 Cambridge Instr Co Inc Gas analyzer

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3683671A (en) * 1970-09-14 1972-08-15 Univ Kansas State Measuring system including thermal conductivity detector means
US3864959A (en) * 1971-12-16 1975-02-11 Pye Ltd Thermal conductivity detector apparatus
US4835108A (en) * 1986-07-28 1989-05-30 The Babcock & Wilcox Company Method for measuring free oxygen in a combustible atmosphere
US4741198A (en) * 1986-10-06 1988-05-03 Beckman Industrial Corporation Thermal conductivity detector assembly
US5297419A (en) * 1992-07-16 1994-03-29 Thermco Instrument Corporation Linearizing gas analyzer
US20130133403A1 (en) * 2009-11-25 2013-05-30 Siemens Aktiengesellschaft Method and Arrangement for Gas Chromatographic Analysis of a Gas Sample
US9116160B2 (en) * 2009-11-25 2015-08-25 Siemens Aktiengesellschaft Method and arrangement for gas chromatographic analysis of a gas sample

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