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US2174923A - Gas analyzer - Google Patents

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US2174923A
US2174923A US151146A US15114637A US2174923A US 2174923 A US2174923 A US 2174923A US 151146 A US151146 A US 151146A US 15114637 A US15114637 A US 15114637A US 2174923 A US2174923 A US 2174923A
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filament
gases
gas
cell
combustibles
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Labino Dominick
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OI Glass Inc
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Owens Illinois Glass 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
    • G01N27/62Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating the ionisation of gases, e.g. aerosols; by investigating electric discharges, e.g. emission of cathode
    • G01N27/626Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating the ionisation of gases, e.g. aerosols; by investigating electric discharges, e.g. emission of cathode using heat to ionise a 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
    • Y10T436/21Hydrocarbon
    • Y10T436/218Total hydrocarbon, flammability, combustibility [e.g., air-fuel mixture, etc.]

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  • the present invention relates to a method and apparatus for detecting the presence of and degree of combustion, and more particularly for analyzing automatically and continuously the combustible gas content of waste gases emanating from a gas fired furnace.
  • One of the objects of the invention is to provide a method and apparatus for indicating and recording the combustible gas contents such as 10 carbon monoxide, hydrogen, hydrocarbons, or the like, that are found by test in the canals of gas fired furnaces, such as a glass furnace, or the like.
  • gases in percentage should be very low at all times, and, for highest efliciency, none of these gases should be present.
  • the percentage of carbon monoxide alone shown by Orsat analysis ranges generally from about zero to two or three per cent or sometimes more.
  • Another object of the invention is to provide an apparatus for this purpose which is extremely simple and inexpensive, and may be constructed and put into operation at a cost far below that whichhas heretofore been found possible for this type of apparatus.
  • I aim to eliminate the use of chemicals or other expensive substances which have heretofore been used as, for example, those used in an Orsat apparatus tc analyze the waste gases.
  • Fig. 1 is a diagrammatic view of my apparatus indicating an electrical hookup used and the manner of connection with a conventional gas fired furnace;
  • Fig. 2 is a perspective view shown partly in section of an arrangement of elements within my analyzing cell.
  • my invention contemplates conducting a clean sample of the stack gases at a predetermined rate and at a. predetermined temperature, and mixed with a predetermined quantity of atmospheric air, through a cell com- 10 posed of a heated filament and a target 01 plate adapted to receive electrons from the heated filament at a rate which varies directly with the amount of combustibles present in the gases passing therethrough.
  • the heated filament causes 15 combustion of the said combustible gases with the oxygen in the admixed air, causing it to ionize the gaseous particles and facilitate the transmission of electrons from the filament to the target or plate.
  • the electrons impinge upon the target or plate they cause the voltage or current to vary in accordance with the rate of impingement.
  • This voltage or current variation may then be amplifieciin any suitable manner, its value regg istered, and, if desired, recorded continuously.
  • reference character 4 designates a gas fired furnace such as a regenerative glass furnace having checkerwork regenerators 5 and 6 which alter- 30 nately communicate with a stack 1 through the regenerator canals 8 and 9, a reversing valve l0, and a stack canal H.
  • the reversing valve II] is reversed, first, to admit air through the air intake l2 through, for 335 example, regenerator canal 8, to the regenerator 5, during which interval the exhaust gases pass through regenerator 6, the regenerator canal 9, the stack canal II, and the stack 1; and then, after a suitable interval, when the reversing valve 40 Ill is reversed, the air is admitted into regenerator 6, and the exhaust gases pass through regenerator 5 out through the stack 1.
  • the sample may then be mixed with a suitable quantity of oxygen or air which may be drawn through the inlet means 20 and mixed in the mixing chamber 2
  • a suitable quantity of oxygen or air which may be drawn through the inlet means 20 and mixed in the mixing chamber 2
  • the exact proportion in which the air and gas sample may be intermixed may be regulated by means of the valves 23 and 24, respectively.
  • Orifices 25 and 26 and accompanying manometers 21 and 28, respectively, may be provided to indicate the relative rates of admixture of the gases and the proportions thereof.
  • the sample is drawn by means of a suitable vacuum pump or exhausting means such as an aspirator 30 through the conduit 3
  • Suitable proportions of air to waste gas for relatively low percentage of combustibles may be about 1 to 1.
  • the rate of passing the gases through the cell 32 may be any desired rate, although I have found that a total of 500 cc. per minute, or 250 cc. of air and 250 cc. of waste gas per minute to be satisfactory.
  • the air needs only be added to the sample in the event that there is no excess air in the waste gas issuing from the furnace. If there is suflicient air or free oxygen present in the waste gas sample, the appartus will continue to record the combustibles present in the gas.
  • the cell 32 is provided with a filament 35, which is preferably composed of a noble metal such as platinum or alloys thereof, owing to its catalytic properties and to the fact that it has a much higher melting temperature compared to other elements which oxidize at elevated temperatures in the presence of oxygen.
  • a variable transformer 38 consisting of a primary 31 communicating with a power line 38, and a secondary 39, communicating with the filament 35, supplies sufiicient current for the filament 35.
  • the cell 32 is also provided with a target, plate or element 40 to which electrons travel from the filament 35, and cause a fluctuation of the voltage or current of plate 40.
  • the plate 40 is directly connected to an ainplifying means comprising a'tube 45 consisting of a filement 46, a grid 41 to which the plate 40 is electrically connected, and a plate 48'.
  • the filament 45 may be energized by an individual secondary 49 of the transformer 36 operating from the same primary 31 as the secondary 39.
  • may be provided between the secondary 49 and the filament 46 for adjustment purposes.
  • the plate 48 is also electrically connected to the secondary 49 of the transformer through a voltage indicator 53 and a B battery 54 which may supply any suitable voltage.
  • a recorder 56 may also be provided in connection with the indicator 53 in order to continuously record the voltage fiuc tuations of the plate 48 as registered by the indicator 53.
  • the voltage fluctuations recorded may be from 0 to about 50 millivolts.
  • the plate voltage should preferably be adjusted by means of the resistor 5
  • the plate voltage should be adjusted so that a fairly uniform scale may be obtained.
  • the range of the indicator 53 and recorder 56 in per cent combustibles as expressed in millivolts, indicated and recorded, will determine the voltage to be used at the plate 48.
  • I preferably provide a variable condenser 60 having any suitable range of capacitance, generally in the range of about .001 microfarad, as a bypass around the cell 32.
  • the condenser 50 may be electrically connected between the plate 40 and the filament 35.
  • Fig. 2 For a detailed view of cell 32, showing a. preferable embodiment thereof, reference may be had to Fig. 2 in which the filament is in the form of a small coil composed of a platinum wire, and the plate or target is in the form of a small screen disposed cylindrically around the filament 35.
  • the element or plate 40 may be composed of any suitable metal such as brass or nickel or a suitable alloy.
  • the operating temperature of the plate 40 is relatively cold compared to the temperature of the filament 35.
  • the plate 40 may be relatively small as, for example, one inch square or so, in order to produce satisfactory results, although the size may be varied as desired within wide limits.
  • the cell 32 may be enclosed in any suitable vessel such as a glass container or the like.
  • the sample of gas to be analyzed is cleaned and intermixed with a constant proportion of air, and is fed through the cell 32 at a constant rate by means of the vacuum pump 30.
  • the filament 35 which is heated to the ignition temperature of at least about 1250 to 1400 F. which is sufiiciently high to ignite the various combustible constituents which may be present in the gas.
  • the most important is generally carbon monoxide, although hydrogen, ethane, methane, and other constituents may be present.
  • the filaments should be sufficiently hot in order to ignite any of the gases which may pass through the cell 32.
  • the conductivity of the gaseous medium between the filament 35 and the element 40 increases in direct proportion to the percentage of combustibles present.
  • the gaseous medium between the filament 35 and the element 40 is ionized in direct proportion to the percentage of combustibles present in the gas which are caused to ignite by the heat of the filament 35.
  • the change in electron fiow passing through the cell 32 from the filament 35 to the element 40 changes the potential at the grid 41 in the tube 45, this change being amplified on the plate 48 and from there indicated by the indicator 53, and if desired, recorded by the recorder 56.
  • the indicator may be a sensitive volt meter recording the voltages from about 0 to about 50 or 100 millivolts, and these millivolts may be calibrated against percentage of combustibles present.
  • the indicator 53 may be made to assume a positive reading, this potential reading resulting from the constants, (l) the capacity of the vari able condenser 60, (2) the filament current in tube adjusted by resistor 5
  • the function of the condenser 80 is to adjust the indicator 53 to zero in percent of combustibles when air and no waste gases are passing through the cell. The number of millivolts then indicated by the indicator 53 becomes zerocof combustibles on the scale.
  • my novel apparatus may be used as a flame indicator or to operate a relay to signal when flames are present in stacks or other parts of gas fired furnaces.
  • no orifice or pumping system is required, and the elements of cell 32 would merely be located in the region requiring observation.
  • the elements in cell 32 should preferably be properly insulated and shielded. when flames-are present, the electrical conductivity between the filament 35' and the element 40 increases, and thus permits the presence of flame to be made manifest.
  • rectified alternating current may be used-in place of that supplied by battery 54.
  • the method of measuring the degree of combustibles in a gas which comprises igniting the combustibles in the gasand simultaneously registering the electrical conductivity change in the gas as the said combustibles are ignited.
  • the method of analyzing a waste gas sampie to determine the degree of combustibles remaining therein comprises admixing suflicient oxygen with said gas to permit complete oxidation of the combustibles therein, raising the gas mixture to ignition temperature of said combustibles to cause combustion of said combustibles, passing an electrical current through said combustible matter in a waste gas sample which j comprisesa cell," means for passing a sample of gas as the combustibles are being ignited, and indicating the amperage changes of-said current.
  • the method of analyzing stack gas contain-, ing combustible gases which comprises adding to said stack gas suiiicient women to permit complete combustion of the combustible gases, passing said mixture of gas between a heated filament and a plate, the temperature of said filament being sumciently high to permit complete combustion of said combustible material in said gases, passing an electrical current through saidgases between said filament and said plate, amplifying said current changes. caused by said combustion, and indicating said amplified current changes.
  • the method of determining the degree of combustible gases in a waste gas sample which comprises igniting said combustible gases with oxygen in the presence of a catalyst, and registering the electrical conductivity of the gases as the combustible matter is burning, the electrical conductivity varying in direct proportion to the percentage of combustible matter in said waste ases.
  • Apparatus -for indicating the percentage of combustible matter in a waste gas sample from a gas fired furnace which comprises a cell, means for passing a sample of said waste gases through said cell at a constant rate, means for admixing a sufiicient quantity of air with said waste gases in said sample prior to entering said cell to cause complete combustion thereof, a filament within said cell, means to energize said filament with alternating current to at least combustion temperatures of said combustible matter, an element spaced apart i'rom said filament and adapted to receive electrons emanating from said heated filament, and means for amplifying and registerregistering the amplified rate of electron flow from said tube, and a capacitance shunting said filament.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Physics & Mathematics (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
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  • Investigating Or Analyzing Materials By The Use Of Electric Means (AREA)

Description

Oct. 3, 1939.
D. LABINO 2,174,923
GA S ANALYZ ER Filed June 30, 195'? REC-0R DER 1a -i l l l l l Dominic/r L abz'no AT RNEYS INVENTOR Patented Oct. 3, 1939 UNITED STATES GAS ANALYZER Dominick Labino, Clarion, Pa., assignor to Owens- Illinois Glass Company, a corporation of Ohio Application June 30, 1937, Serial No. 151,146
7 Claims.
The present invention relates to a method and apparatus for detecting the presence of and degree of combustion, and more particularly for analyzing automatically and continuously the combustible gas content of waste gases emanating from a gas fired furnace.
One of the objects of the invention is to provide a method and apparatus for indicating and recording the combustible gas contents such as 10 carbon monoxide, hydrogen, hydrocarbons, or the like, that are found by test in the canals of gas fired furnaces, such as a glass furnace, or the like. These gases in percentage should be very low at all times, and, for highest efliciency, none of these gases should be present. However, the percentage of carbon monoxide alone shown by Orsat analysis ranges generally from about zero to two or three per cent or sometimes more. By
continuously indicating and recording the percentage of combustibles in the waste gases, ad-
justments may be made to keep the combustlbles as low as possible, and at the same time avoid an excess of air over the optimum proportions.
Heretofore various means have been provided for electrically analyzing the combustibles present in stack gases, as, for example, by registering the ohmic resistance of a platinum wire which is raised to ignition temperature, and is placed in a cell in which samples of the stack gases are continuously passing. This method I have found to be inaccurate and unreliable after a short period of time owing apparently to the attack of the gases upon the platinum wire which seems to be changed in its catalytic behavior. It is an object of the invention to overcome these diiiiculties and to provide an instrument which will continuously and accurately record the percentage of combustibles present, and to do this for a long period of time.
Another object of the invention is to provide an apparatus for this purpose which is extremely simple and inexpensive, and may be constructed and put into operation at a cost far below that whichhas heretofore been found possible for this type of apparatus. In this connection I aim to eliminate the use of chemicals or other expensive substances which have heretofore been used as, for example, those used in an Orsat apparatus tc analyze the waste gases.
Other objects and advantages of the present invention will become apparent from the following description taken in conjunction with the drawing in which:
Fig. 1 is a diagrammatic view of my apparatus indicating an electrical hookup used and the manner of connection with a conventional gas fired furnace; and
Fig. 2 is a perspective view shown partly in section of an arrangement of elements within my analyzing cell.
Generally speaking, my invention contemplates conducting a clean sample of the stack gases at a predetermined rate and at a. predetermined temperature, and mixed with a predetermined quantity of atmospheric air, through a cell com- 10 posed of a heated filament and a target 01 plate adapted to receive electrons from the heated filament at a rate which varies directly with the amount of combustibles present in the gases passing therethrough. The heated filament causes 15 combustion of the said combustible gases with the oxygen in the admixed air, causing it to ionize the gaseous particles and facilitate the transmission of electrons from the filament to the target or plate.
As the electrons impinge upon the target or plate, they cause the voltage or current to vary in accordance with the rate of impingement. This voltage or current variation may then be amplifieciin any suitable manner, its value regg istered, and, if desired, recorded continuously.
Referring now more particularly to Fig. 1, reference character 4 designates a gas fired furnace such as a regenerative glass furnace having checkerwork regenerators 5 and 6 which alter- 30 nately communicate with a stack 1 through the regenerator canals 8 and 9, a reversing valve l0, and a stack canal H. At predetermined intervals the reversing valve II] is reversed, first, to admit air through the air intake l2 through, for 335 example, regenerator canal 8, to the regenerator 5, during which interval the exhaust gases pass through regenerator 6, the regenerator canal 9, the stack canal II, and the stack 1; and then, after a suitable interval, when the reversing valve 40 Ill is reversed, the air is admitted into regenerator 6, and the exhaust gases pass through regenerator 5 out through the stack 1.
It is the purpose of the present invention to analyze the exhaust gases passing through the canals 8, 9, and/or l0, and accordingly suitable conduits l5, l6 and I! may be provided communicating with these canals respectively, these conduits leading to a selector valve [8, and then 50 through a suitable filter and drier l9. This drier may be supplied with calcium chloride or other suitable substance adapted to remove the water from the gas sample. The removal of water and foreign particles protects the internal parts of 55 the apparatus from corrosion or clogging as well as preventing faulty readings.
The sample may then be mixed with a suitable quantity of oxygen or air which may be drawn through the inlet means 20 and mixed in the mixing chamber 2|. The exact proportion in which the air and gas sample may be intermixed may be regulated by means of the valves 23 and 24, respectively. Orifices 25 and 26 and accompanying manometers 21 and 28, respectively, may be provided to indicate the relative rates of admixture of the gases and the proportions thereof.
From the mixing chamber 2|, the sample is drawn by means of a suitable vacuum pump or exhausting means such as an aspirator 30 through the conduit 3| and through the ignition cell 32.
Suitable proportions of air to waste gas for relatively low percentage of combustibles, as, for example, less than about three per cent combustibles, may be about 1 to 1. The rate of passing the gases through the cell 32 may be any desired rate, although I have found that a total of 500 cc. per minute, or 250 cc. of air and 250 cc. of waste gas per minute to be satisfactory. The air needs only be added to the sample in the event that there is no excess air in the waste gas issuing from the furnace. If there is suflicient air or free oxygen present in the waste gas sample, the appartus will continue to record the combustibles present in the gas.
The cell 32 is provided with a filament 35, which is preferably composed of a noble metal such as platinum or alloys thereof, owing to its catalytic properties and to the fact that it has a much higher melting temperature compared to other elements which oxidize at elevated temperatures in the presence of oxygen. A variable transformer 38 consisting of a primary 31 communicating with a power line 38, and a secondary 39, communicating with the filament 35, supplies sufiicient current for the filament 35.
The cell 32 is also provided with a target, plate or element 40 to which electrons travel from the filament 35, and cause a fluctuation of the voltage or current of plate 40.
The plate 40 is directly connected to an ainplifying means comprising a'tube 45 consisting of a filement 46, a grid 41 to which the plate 40 is electrically connected, and a plate 48'. The filament 45 may be energized by an individual secondary 49 of the transformer 36 operating from the same primary 31 as the secondary 39. A resistor 5| may be provided between the secondary 49 and the filament 46 for adjustment purposes. The plate 48 is also electrically connected to the secondary 49 of the transformer through a voltage indicator 53 and a B battery 54 which may supply any suitable voltage.
I have found satisfactory results may be obtained with a voltage of about 45 volts in the B battery 54 when the voltage of the power line 38 is about-110 volts. A recorder 56 may also be provided in connection with the indicator 53 in order to continuously record the voltage fiuc tuations of the plate 48 as registered by the indicator 53. The voltage fluctuations recorded may be from 0 to about 50 millivolts.
From the particular characteristics of the tube 45, the plate voltage should preferably be adjusted by means of the resistor 5| so that, with minimum changes in grid voltage 41, a straight line grid voltage to plate current 48 is obtained, whereby the percentage of combustibles is directly, although not necessarily uniformly, proportional to the plate current. In other words, the plate voltage should be adjusted so that a fairly uniform scale may be obtained. Ordinarily, the range of the indicator 53 and recorder 56 in per cent combustibles as expressed in millivolts, indicated and recorded, will determine the voltage to be used at the plate 48.
In order to adjust theindicator 53 to zero in per cent of combustibles, I preferably provide a variable condenser 60 having any suitable range of capacitance, generally in the range of about .001 microfarad, as a bypass around the cell 32. Thus, the condenser 50 may be electrically connected between the plate 40 and the filament 35.
For a detailed view of cell 32, showing a. preferable embodiment thereof, reference may be had to Fig. 2 in which the filament is in the form of a small coil composed of a platinum wire, and the plate or target is in the form of a small screen disposed cylindrically around the filament 35. The element or plate 40 may be composed of any suitable metal such as brass or nickel or a suitable alloy. The operating temperature of the plate 40 is relatively cold compared to the temperature of the filament 35. Ordinarily, the plate 40 may be relatively small as, for example, one inch square or so, in order to produce satisfactory results, although the size may be varied as desired within wide limits. The cell 32 may be enclosed in any suitable vessel such as a glass container or the like.
In operating the device, the sample of gas to be analyzed is cleaned and intermixed with a constant proportion of air, and is fed through the cell 32 at a constant rate by means of the vacuum pump 30. As the gas passes through the cell 32, it is ignited by the filament 35 which is heated to the ignition temperature of at least about 1250 to 1400 F. which is sufiiciently high to ignite the various combustible constituents which may be present in the gas. Among these, the most important is generally carbon monoxide, although hydrogen, ethane, methane, and other constituents may be present. The filaments should be sufficiently hot in order to ignite any of the gases which may pass through the cell 32. As the combustibles are ignited by the filament 35, the conductivity of the gaseous medium between the filament 35 and the element 40 increases in direct proportion to the percentage of combustibles present. In other words, the gaseous medium between the filament 35 and the element 40 is ionized in direct proportion to the percentage of combustibles present in the gas which are caused to ignite by the heat of the filament 35. The change in electron fiow passing through the cell 32 from the filament 35 to the element 40 changes the potential at the grid 41 in the tube 45, this change being amplified on the plate 48 and from there indicated by the indicator 53, and if desired, recorded by the recorder 56. The indicator may be a sensitive volt meter recording the voltages from about 0 to about 50 or 100 millivolts, and these millivolts may be calibrated against percentage of combustibles present.
In adjusting the device at the start of operations, the indicator 53 may be made to assume a positive reading, this potential reading resulting from the constants, (l) the capacity of the vari able condenser 60, (2) the filament current in tube adjusted by resistor 5|, (3) the distance between the filament 35 and the plate 40 in cell 32, and (4) the rate of electron or current flow through the cell when air and no waste gases are passing therethrough. The function of the condenser 80 is to adjust the indicator 53 to zero in percent of combustibles when air and no waste gases are passing through the cell. The number of millivolts then indicated by the indicator 53 becomes zerocof combustibles on the scale.
Various other applications may be made with my novel apparatus as, for example, it may be used as a flame indicator or to operate a relay to signal when flames are present in stacks or other parts of gas fired furnaces. In this event, however, of course, no orifice or pumping system is required, and the elements of cell 32 would merely be located in the region requiring observation. However, in this event, the elements in cell 32 should preferably be properly insulated and shielded. when flames-are present, the electrical conductivity between the filament 35' and the element 40 increases, and thus permits the presence of flame to be made manifest.
Various modifications and variations maybe resorted to without departing from the spirit and scope of the present invention, as, for example, rectified alternating current may be used-in place of that supplied by battery 54.
I claim:
1. The method of measuring the degree of combustibles in a gas, which comprises igniting the combustibles in the gasand simultaneously registering the electrical conductivity change in the gas as the said combustibles are ignited.
2. The method of analyzing a waste gas sampie to determine the degree of combustibles remaining therein, which comprises admixing suflicient oxygen with said gas to permit complete oxidation of the combustibles therein, raising the gas mixture to ignition temperature of said combustibles to cause combustion of said combustibles, passing an electrical current through said combustible matter in a waste gas sample which j comprisesa cell," means for passing a sample of gas as the combustibles are being ignited, and indicating the amperage changes of-said current.
3. The method of analyzing stack gas containing combustible gases, which comprise s adding to said stack gas sufllcient oxygen to permit complete combustion of the combustible gases, passing said mixture of gas between a heated filament and a plate, the temperature of said filament being sufiiciently high to permit com plete combustion of said combustible material in said gases, passing electrons through said gases from said filament to said plate, and measuring the changes in the electron flow caused by said combustion.
4. The method of analyzing stack gas contain-, ing combustible gases, which comprises adding to said stack gas suiiicient women to permit complete combustion of the combustible gases, passing said mixture of gas between a heated filament and a plate, the temperature of said filament being sumciently high to permit complete combustion of said combustible material in said gases, passing an electrical current through saidgases between said filament and said plate, amplifying said current changes. caused by said combustion, and indicating said amplified current changes.
5. The method of determining the degree of combustible gases in a waste gas sample, which comprises igniting said combustible gases with oxygen in the presence of a catalyst, and registering the electrical conductivity of the gases as the combustible matter is burning, the electrical conductivity varying in direct proportion to the percentage of combustible matter in said waste ases. I V l 6. Apparatus -for indicating the percentage of combustible matter in a waste gas sample from a gas fired furnace, which comprises a cell, means for passing a sample of said waste gases through said cell at a constant rate, means for admixing a sufiicient quantity of air with said waste gases in said sample prior to entering said cell to cause complete combustion thereof, a filament within said cell, means to energize said filament with alternating current to at least combustion temperatures of said combustible matter, an element spaced apart i'rom said filament and adapted to receive electrons emanating from said heated filament, and means for amplifying and registerregistering the amplified rate of electron flow from said tube, and a capacitance shunting said filament. and the electrical connection between said grid and said element V r 7. Apparatus for indicating. the percentage of waste gases through said'cell ata constant rate and admixed with sufllcient oxygen to oxidize the combustible'matter in said cell and cause com- :plete combustion thereof, a filament within said .the grid thereof electrically connected to said target, alternating current energizing means for the filament of said detector tube, means for registering the electrical energy emanating from the plate of said detector tube, and a capacitance shunting the filament within said cell with the electrical connection between said grid and said DOMINIC'K m0.
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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2448111A (en) * 1945-05-05 1948-08-31 Nicolai Arduo Lewis Method and apparatus for measuring constituents of gases
US2622967A (en) * 1945-03-07 1952-12-23 Union Carbide & Carbon Corp Automatic gas ratio sampling device
US2934578A (en) * 1959-02-20 1960-04-26 Milton D Scheer Process for low temperature hydrogenation of olefins
US3484773A (en) * 1968-01-10 1969-12-16 Erdco Eng Corp Combustible gas detector apparatus

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2622967A (en) * 1945-03-07 1952-12-23 Union Carbide & Carbon Corp Automatic gas ratio sampling device
US2448111A (en) * 1945-05-05 1948-08-31 Nicolai Arduo Lewis Method and apparatus for measuring constituents of gases
US2934578A (en) * 1959-02-20 1960-04-26 Milton D Scheer Process for low temperature hydrogenation of olefins
US3484773A (en) * 1968-01-10 1969-12-16 Erdco Eng Corp Combustible gas detector apparatus

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