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GB2155184A - Combined sensor device for detecting toxic gases - Google Patents

Combined sensor device for detecting toxic gases Download PDF

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Publication number
GB2155184A
GB2155184A GB08503514A GB8503514A GB2155184A GB 2155184 A GB2155184 A GB 2155184A GB 08503514 A GB08503514 A GB 08503514A GB 8503514 A GB8503514 A GB 8503514A GB 2155184 A GB2155184 A GB 2155184A
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component
signal
heating
product
gas
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GB2155184B (en
GB8503514D0 (en
Inventor
Joseph Robert Stetter
Solomon Zaromb
Melvin Walker Findlay
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US Department of Energy
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US Department of Energy
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Publication of GB2155184A publication Critical patent/GB2155184A/en
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    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/0004Gaseous mixtures, e.g. polluted air
    • G01N33/0009General constructional details of gas analysers, e.g. portable test equipment
    • G01N33/0011Sample conditioning
    • G01N33/0013Sample conditioning by a chemical reaction
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/0004Gaseous mixtures, e.g. polluted air
    • G01N33/0009General constructional details of gas analysers, e.g. portable test equipment
    • G01N33/0027General constructional details of gas analysers, e.g. portable test equipment concerning the detector
    • G01N33/0031General constructional details of gas analysers, e.g. portable test equipment concerning the detector comprising two or more sensors, e.g. a sensor array
    • G01N33/0032General constructional details of gas analysers, e.g. portable test equipment concerning the detector comprising two or more sensors, e.g. a sensor array using two or more different physical functioning modes

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Pathology (AREA)
  • Food Science & Technology (AREA)
  • Medicinal Chemistry (AREA)
  • Combustion & Propulsion (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Investigating Or Analyzing Materials By The Use Of Electric Means (AREA)
  • Investigating Or Analyzing Materials By The Use Of Fluid Adsorption Or Reactions (AREA)
  • Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)

Abstract

An instrument capable of detecting low concentrations of a pollutant or other component in air or other gas, includes a combination of a heating filament (10) having a catalytic surface (14) of a noble metal for exposure to the gas and producing a derivative product from the component, and an electrochemical sensor, including sensing, (18), counter (21) and reference (22) electrodes, responsive to the derivative product for providing a signal indicative of the product the gas passing via inlet (26) and outlet (28). At concentrations in the order of about 1-100 ppm of tetrachloroethylene, neither the heating filament nor the electrochemical sensor is individually capable of sensing the pollutant. In the combination, the heating filament converts the benzyl chloride to one or more derivative products which may be detected by the electrochemical sensor. In another arrangement the heated filament may also act as a sensor which emits a signal if the presence of pollutant is at a concentration above 0.5 to 1% which signal operates a valve to cause the derivative formed by the filament to be directed away from the electrochemical sensor. If no signal is produced the derivative passes to the electrochemical sensor. <IMAGE>

Description

SPECIFICATION Combined sensor device for detecting toxic gases This invention relates to devices for detecting pollutants and more particularly to devices capable of detecting pollutants at relatively low concentrations in ambient gases. Electrochemical sensing devices, especially amperometric sensors such as those disclosed in U.S. Patent Nos. 3,776,832, 4,201,634 and 4,326,927 offer the advantages of portability, real-time readout, relatively low cost, and fair sensitivity and selectivity to a few specific pollutants such as CO, H2S, NO, NO2, SO2, hydrazine, COCI2, HCN, or Cl2. However, these devices are not applicable, at present to the detection of many species that are not electrochemically active.
In detecting pollutants including toxic substances, sensing devices have usually been limited with respect to concentrations of the pollutants particularly when the pollutants are essentially not electrochemically active or have an activity difficult to detect. Below certain values of concentration, e.g., 100 ppm (parts per million) of benzyl chloride, tetrachloroethylene or the like, presently available portable devices are essentially unresponsive to the pollutant. Since some pollutants may be extremely toxic, it is important to develop devices for detecting various pollutants at low concentrations.
Accordingly, one object of this invention is a device for detecting pollutants at low concentrations in gases. Another object is an electrochemical device for detecting pollutants in ambient gases where the pollutants are essentially electrochemically inactive or have an activity difficult to detect.
An additional object is a device which may be utilized as a portable instrument to survey an area or as a site monitor for a wide variety of gases. A further object is a device which is also capable of detecting pollutants at higher concentrations, at which level they may present an acute toxicity or flammability hazard.
Briefly, the invention relates to a device for detecting a pollutant in an ambient gas and comprises (1) electrical conversion means having a catalytic surface to chemically convert the pollutant (e.g., a hydrocarbon) to a derivative product (e.g., carbon monoxide) having a characteristic electrochemical activity, and (2) electrochemical sensing means responsive to that electrochemical activity and providing a signal indicative of the derivative product and thereby the original pollutant. in one embodiment, the conversion means includes a sensor responsive to higher concentrations of an electrochemically inactive pollutant, but essentially unresponsive to lower concentrations, and an electrochemical sensor responsive to the derivative product, but essentially unresponsive to the pollutant at low concentrations.The conversion means may comprise a heated filament made of or coated with a noble metal catalyst, such as Pt, Pd, Ir, Rh, Au, Ag, or an alloy or compound of one of such metals.
Figure 1 is an exploded view of one embodiment of the invention.
Figure 2 is a cross-sectional view of yet another embodiment of the invention.
Figure 3 is a flow diagram of yet another embodiment of the invention.
Figure 4 shows representative response curves for benzene from devices constructed according to the invention.
The device of the invention is suitable for use in detecting at least one of a variety of pollutants or otherwise hazardous gases or vapors in ambient gas. These pollutants commonly include various organic compositions such as benzene, benzyl chloride, toluene, methane, tetrachloroethylene, tetrahydrofuran, cyclohexane and the like. It is particularly useful for detecting the presence of a pollutant such as benzyl chloride or benzene at low concentrations in the order of about 1-100 ppm where some sensing devices are inoperative. In addition, the device may be constructed of components permitting its use as a portable instrument capable of on-site detection of a pollutant and in some instances fixed site analysis of the general concentration of the pollutant.
The device includes in combination, electrical heating means having a noble metal exposed surface for chemically changing the pollutant to a derivative product having a characteristic electrochemical activity and a sensing means responsive to the electrochemical activity of the product and including signal means providing a signal indicative of the product and thereby the pollutant. The derivative product results from the chemical change in the pollutant which may occur from the oxidation or other process on the pollutant to either form electrochemical activity or change the existing activity of the pollutant.A particularly useful combination for the device includes a noble metal heating means which also operates as a sensor providing a signal at concentrations of the pollutant above about 0.11.0% while providing the derivative product over the overall concentration range for detection by the electrochemical sensing means. The presence or absence of the signal from the noble metal heating means in combination with the signal from the electrochemical sensing means may be used in determining the presence or absence of a pollutant and its general concentration range.
The derivative product from the pollutant exhibits a characteristic electrochemical activity which may be detected by the sensing means at levels as low as about one ppm. These products may be the oxides of carbon, sulfur, nitrogen and the like having electrochemical activity and other compositions indicative of partial oxidation or decomposition of the pollutant.
The device of Figure 1 includes the catalytic heating means as illustrated by a hot-wire sensor arranged to receive a sample of the ambient gas and sensing means illustrated by an electrochemical sensor arranged to receive the derivative product. The conversion means may include a signal means for providing a signal apart from the signal from the sensing means. The hot-wire sensor includes a heating means and a catalyst such as one or more of the oxidation catalysts. In general, hotwire sensors and catalysts based on Pt, Pd, Rh and Au are particularly useful. Also useful may be catalysts comprising Ir or Ag, or various noble metal alloys, such as Pd-Ag, Pt-Rh, Pt-lr or Au-Ag, or a compound, especially an oxide, of one of said metals. The hot wires or filaments may be either made of a pure noble metal or, preferably, be coated on a suitable baser metal or alloy.The catalysts may also be dispersed on a support such as C, Si or alumina. As the sample is exposed to the hot catalyst, it is chemically changed and preferably oxidized or decomposed to at least one derivative product which may be detected by the electrochemical sensor.
The electrochemical sensor is responsive to low levels of the derivative product and provides a signal indicative of the product and thereby the pollutant. While the electrochemical sensor is responsive to some electrochemically active substances at these low levels, its response to compounds such as benzyl chloride and the like which are not primarily characterized by electrochemical activity tends to be so limited that it may not be used for detection unless aided by one of the above-mentioned oxidation catalysts.
Suitably, the electrochemical sensor may be a constant-potential amperometric sensor. As the derivative product is sensed, a signal is generated indicative of the electrochemical activity at the "working electrode" of the sensor. In general, the hot wire sensor representing the conversion means and the amperometric chemical sensor representing the sensing means are sufficiently small that they may be built into a single unit where the derivative product from the hot wire sensor may interact with the electrochemical sensor within the same unit. Preferably, the sample is introduced into a sample channeling arrangement by which the sample is first introduced to the hot-wire sensor.The derivative product from the hot-wire sensor is then routed to the electrochemical sensor either directly, but in a controlled manner, so as to enhance the activity of said sensor by raising its temperature to a preferred value or through a baffle arrangement or other isolation system so that the electrochemical sensor need not be directly exposed to the heater of the hot-wire sensor In Figure 1, an exploded view of the invention is illustrated showing a path including a baffle arrangement to isolate the electrochemical sensor from the heater of the hot-wire sensor and thereby reduce the possibility of damage to the electrochemical sensor.
The inventive device includes electrical heating means with a noble metal surface exposed to the gas for heating the gas and catalyzing the combustion of the pollutant to provide a derivative product having a characteristic electrochemical activity and electrochemical sensing means responsive to that activity for providing a signal indicative of that activity. As illustrated in Figure 1, the heating means is provided by a filament 10 composed of a heating element core 12 and a noble metal surface 14 mounted in a reaction chamber 16 of block 15. A sensing element 18 is mounted in chamber 20 of block 19 for detecting the electrochemical activity of the product derived from the combustion of the pollutant. A reference electrode 22 and a counter electrode 21 are also provided. Blocks 15 and 19 are joined by block 23 with chamber 24.Inlet 26, outlet 28 and chambers 16 and 24 provide channeling means for exposing the gas to the heating filament 10 and the derivative product to the sensing element 18. Closure member 30 provides sealing of chamber 20. A pluggable opening 32 above chamber 20 permits introduction of electrolyte into the electrochemical sensor.
In another embodiment of the invention, shown in Figure 2, a diffusion-type electrochemical sensor is used to detect concentrations of 0-2.4% methane in air by preexposing any ambient gas diffusing or convecting towards said sensor to an iridiumcoated filament heated to a temperature of 300 600"C and preferably 400-500"C. The filament is made preferably of a metal or alloy of relatively high resistivity having a coefficient of thermal expansion close to that of iridium, e.g., commercial grade titanium. By adjusting the filament length and cross-section to yield a resistance of about 2,000 ohms and temperature of 40Q500"C when heated by a current of about 10 milliamperes, it becomes possible to achieve a low-power low-current-drain methane detector suitable for intrinsically safe mine-monitoring applications.
In Figure 2 the device 36 includes heating filament 38 mounted in housing 37 with electrochemical sensing element 40 hidden from direct exposure to filament 38 by barrier 42 of glass wool or other suitable porous material. In Figure 2, inlet 52, vent 46, and channels 48, 49 and 50 provide channeling of the gas and derivative product. A source of electrical current is provided by leads 54 and 56 passing through a ceramic plug 44 to filament 38.
The heating of the iridium-coated filament of Figure 2 is preferably governed by a temperature controller, such as that shown in the block diagram of Figure 3. To further reduce the heating power requirements, the filament may be heated in intermittent pulses, e.g., in pulses of 0.5 to 3 seconds' duration every 10 seconds. In general, the response time of the device is less than about 20 seconds. The heating pulses are sufficient to bring the peak filament temperature up to the range of 400-500"C.
It is noteworthy that electrochemical sensors when used by themselves such as that used in the device of Figure 2, do not usually respond to methane even in concentrations as high as 100%. Yet the signals obtained with the heated iridium filament permit easy measurement of methane concentrations as low as 0.05% or less.
As an illustration of the general flow diagram associated with the detection process, Figure 3 illustrates an arrangement where the derivative product may be automatically routed through a multipath solenoid valve or other diversion means to either the electrochemical sensor or removed from the device before exposure to the sensor de pending on the concentration levels. In this flow arrangement, the signal from the hot-wire sensor may serve to indicate the presence of the pollutant at a concentration above about 0.5-1.0% and may be used to direct the flow of derivative product away from the device to avoid the possible effects of an excessive concentration of certain pollutants on the electrochemical sensor.
When no signal from the hot-wire sensor is provided, the flow pattern will be used to direct the derivative product to the electrochemical sensor and its signal will provide an indication of the presence of the derivative product and thereby the pollutant. With a combination of signals, the presence of the pollutant and its concentration may be determined.
The general flow pattern of the gas and derivative product as illustrated in Figure 3. As illustrated, a gas sample is admitted via line 60 to conversion chamber 62 having filament 64 whose temperature is controlled by controller 65. Signal indicating means is provided by indicator 66 to provide any signal available from filament 64. The derivative product is channeled via line 68, valve 70 and line 72 to the electrochemical sensor 74 having a signal indicator 76. Pump 78 provides the suction and determines the flow rate within the device. Controller 65 and valve 70 are governed by a microprocessor (computer/controller) 79 which receives the signals from indicator 66 and 76.
As an illustration of the representative performance of the above-disclosed embodiments, Figure 4 provides response curves for benzene. In general, benzene is not readily detected on electrochemical sensors at ppm levels and is further essentially undetectable by a hot-wire sensor at ppm levels. However, by combining the two different sensors, it is possible to produce signals indicative of the presence of benzene at a concentration of less than 100 ppm level in air. While benzene at such levels is not detectable by hot-wire or heated semiconductor sensors, the heated catalytic surface of such sensors or other noble metal-coated filaments converts the benzene to one or more oxides of carbon or degradation products which are then detected by the electrochemical sensor.
In Figure 4A, the heated filament was made of a fine platinum wire (0.08 millimeter in diameter) similar to that used in hot-wire flammable gas sensors, heated to a temperature of about 1000 C. The two humps starting at about 1.5 minutes and 4 minutes correspond to exposure to samples of 200 ppm and 50 ppm of benzene, respectively. In Figure 4B, a commercial tin oxide semiconductor sensor, heated to about 300"C, was used as a conversion means. The three humps starting at about 1 minute, 6 minutes, and 10 minutes correspond to samples of 200 ppm, 50 ppm, and 200 ppm of benzene, respectively. In Figure 4C, the conversion device consisted of a fine (0.08 millimeter in diameter) gold filament heated to 950+50 C, and the hump starting at about 0.6 minute was due to a sample of 200 ppm of benzene.The same electrochemical sensor, comprising a platinum black sensing electrode at a potential of about 1.1 volt relative to the standard reversible hydrogen electrode, was used in all three cases. A comparison of the ordinates of Figures 4A, B, and C shows that the heated tin oxide yields an approximately three to four times higher response than the platinum filament, but that the gold filament yields a three-fold higher response than the tin oxide and a ten times higher response than the platinum.
Other representative compounds which do not appear to be detected by either type of sensor independently but are by the two sensors in combination at concentrations of about 100 ppm or less are benzyl chloride and tetrachloroethylene.
The following example is provided for illustrative purposes and is not intended to be restrictive as to the scope of the invention: Example I A sample of air containing 200 ppm of tetrachloroethylene was tested in an apparatus having a catalytic bead sensor available from Rexnord Corporation of Sunnyvale, California and a Pt-catalyzed CO filament available from Energetic Science of Hawthorne, New York. The sample was tested with each element operating separately. Observed currents from each sensor operating separately were indistinguishable from normal noise levels. In another test, a similarly constructed electrochemical sensor in combination with a Pt-catalyzed CO filament was used for an air sample containing only 20 ppm tetrachloroethylene. A signal of about 0.3 microamps was observed for the combination of sensors as compared to a value of less than 0.2 (noise level) microamps without the filament.
As described above, the invention provides a useful device for detecting a gas, vapor, chemical pollutant or other component in a gaseous medium and is capable by a combination of a catalytic heating element and an electrochemical sensor of detecting the component at low concentrations.
The foregoing description of embodiments of the invention has been presented for purposes of illustration and description. It is not intended to be exhaustive or to limit the invention to the precise form disclosed, and obviously many modifications and variations are possible in light of the above teaching.

Claims (25)

1. A device for detecting a gas, vapor, chemical pollutant or other component of interest in a gaseous medium comprising electrical heating element means including a noble metal-containing catalytic surface exposed to the gas for heating the gas for catalytically producing a derivative product of said component having a characteristic electrochemical activity, and electrochemical sensing means arranged for exposure to the derivative product, responsive to the electrochemical activity of the product, and capable of producing a signal in response thereto.
2. The device of Claim 1 including at least one additional heating element means with a different catalytic surface exposed to said gas.
3. The device of Claim 1 including means for passing an electrical current through said heating means and means for measuring the signal from said sensing means.
4. The device of Claim 3 including means for interrupting the electrical current through said heating means.
5. The device of Claim 4 wherein said interruption means generates heat pulses of a predetermined duration at predetermined time intervals.
6. The device of Claim 1 wherein said catalyst is based on Pt.
7. The device of Claim 1 wherein said catalyst is based on Au.
8. The device of Claim 1 wherein said catalyst is based on Ir.
9. The device of Claim 1 wherein said catalyst is based on Pd.
10. The device of Claim 1 wherein said catalyst is based on Rh.
11. The device of Claim 1 wherein said catalyst is based on a mixture of Pd and Ag.
12. The device of Claim 5 including a plurality of said heating means with different catalytic surfaces.
13. The device of Claim 5 wherein said heating means has a core material with an electrical resistivity above that of the noble metal and with a coefficient of thermal expansion comparable to that of the noble metal.
14. The device of Claim 1 wherein the heating means and sensing means are selected to be capable of providing a signal indicative of said component at concentrations below about 0.1%.
15. The device of Claim 1 including channeling means for directing said gas to said heating means and said product to said sensing means.
16. The device of Claim 15 wherein said channeling means includes means for preventing direct exposure of said sensing element to said heating means.
17. The device of Claim 1 wherein said heating means includes signal means for providing a signal indicative of said component.
18. The device of Claim 16 wherein said heating means includes signal means for providing a signal indicative of said component and said channeling means includes means for diverting said product from exposure to said sensing means.
19. A device for detecting a component of an ambient gas comprising conversion means for chemically changing said component to a derivative product having a characteristic electrochemical activity, said conversion means having a first means for generating a signal when said component is present in a concentration above about 0.1-1.0%, but essentially unresponsive at concentrations below about 0.1%, and sensing means responsive to the electrochemical activity of said product for concentration of said component below about 0.1% for providing a signal indicative of the product and thereby the component.
20. The device of Claim 19 including means for receiving the signals from said conversion and sensing means and determining the general concentration of said component.
21. The device of Claim 19 where said conversion means is a hot wire sensor having a surface of an oxidation catalyst.
22. The device of Claim 20 wherein said sensing means is an electrochemical sensor operative with oxidized gases of organic compositions.
23. The device of Claim 19 wherein said conversion means is a semiconductor sensor.
24. The device of Claim 23 wherein said semiconductor is a metal oxide.
25. The device of Claim 24 wherein said metal oxide is tin oxide or a mixture thereof.
GB08503514A 1984-03-02 1985-02-12 Combined sensor device for detecting toxic gases Expired GB2155184B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US58572184A 1984-03-02 1984-03-02

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GB8503514D0 GB8503514D0 (en) 1985-03-13
GB2155184A true GB2155184A (en) 1985-09-18
GB2155184B GB2155184B (en) 1988-04-13

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GB08503514A Expired GB2155184B (en) 1984-03-02 1985-02-12 Combined sensor device for detecting toxic gases
GB08629014A Expired GB2184244B (en) 1984-03-02 1986-12-04 Device for detecting a component of an ambient gas

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GB08629014A Expired GB2184244B (en) 1984-03-02 1986-12-04 Device for detecting a component of an ambient gas

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JP (1) JPS60205348A (en)
CA (1) CA1261720A (en)
DE (1) DE3507385A1 (en)
FR (1) FR2560685B1 (en)
GB (2) GB2155184B (en)
IT (1) IT1184147B (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3729286A1 (en) * 1987-09-02 1989-03-16 Draegerwerk Ag MEASURING DEVICE FOR ANALYZING A GAS MIXTURE
GB2218523A (en) * 1988-02-29 1989-11-15 Atomic Energy Authority Uk Sensing the composition of gas
US12480923B2 (en) * 2022-09-07 2025-11-25 Kabushiki Kaisha Toshiba Chemical sensor system

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3624509A1 (en) * 1980-09-26 1988-06-30 Maria Gyulai Dr Dobosne Arrangement and process for detecting halogen-containing compounds
GB2482335B (en) * 2010-07-30 2012-09-19 Thermo Electron Mfg Ltd Apparatus and method for combustion analysing a sample

Citations (5)

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Publication number Priority date Publication date Assignee Title
GB2017315A (en) * 1978-03-22 1979-10-03 Bayer Ag Apparatus for detecting traces of gas
GB2047898A (en) * 1979-03-15 1980-12-03 Ricardo Consulting Engs Ltd Method and apparatus for measuring the air/fuel ratio supplied to a combustion system
GB2098741A (en) * 1981-05-13 1982-11-24 Draegerwerk Ag Method of and apparatus for measuring the quantity of an anaesthetic in a gas
GB2099588A (en) * 1981-05-28 1982-12-08 Nat Res Dev Fluid component measuring and alarm device
EP0098716A1 (en) * 1982-07-02 1984-01-18 The Babcock & Wilcox Company Calorimeters for and methods of monitoring calorific values of gases

Family Cites Families (1)

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Publication number Priority date Publication date Assignee Title
GB2034893A (en) * 1978-11-17 1980-06-11 English Electric Valve Co Ltd Combustible gas detector

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2017315A (en) * 1978-03-22 1979-10-03 Bayer Ag Apparatus for detecting traces of gas
GB2047898A (en) * 1979-03-15 1980-12-03 Ricardo Consulting Engs Ltd Method and apparatus for measuring the air/fuel ratio supplied to a combustion system
GB2098741A (en) * 1981-05-13 1982-11-24 Draegerwerk Ag Method of and apparatus for measuring the quantity of an anaesthetic in a gas
GB2099588A (en) * 1981-05-28 1982-12-08 Nat Res Dev Fluid component measuring and alarm device
EP0098716A1 (en) * 1982-07-02 1984-01-18 The Babcock & Wilcox Company Calorimeters for and methods of monitoring calorific values of gases

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3729286A1 (en) * 1987-09-02 1989-03-16 Draegerwerk Ag MEASURING DEVICE FOR ANALYZING A GAS MIXTURE
GB2218523A (en) * 1988-02-29 1989-11-15 Atomic Energy Authority Uk Sensing the composition of gas
GB2218523B (en) * 1988-02-29 1992-09-02 Atomic Energy Authority Uk Gas sensing
US12480923B2 (en) * 2022-09-07 2025-11-25 Kabushiki Kaisha Toshiba Chemical sensor system

Also Published As

Publication number Publication date
FR2560685B1 (en) 1989-05-12
IT1184147B (en) 1987-10-22
GB2184244A (en) 1987-06-17
JPS60205348A (en) 1985-10-16
GB2155184B (en) 1988-04-13
IT8519721A0 (en) 1985-03-01
GB8503514D0 (en) 1985-03-13
DE3507385A1 (en) 1985-09-05
CA1261720A (en) 1989-09-26
GB8629014D0 (en) 1987-01-14
GB2184244B (en) 1988-04-07
FR2560685A1 (en) 1985-09-06

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PCNP Patent ceased through non-payment of renewal fee

Effective date: 19970212