US2473525A - Atmosphere production - Google Patents
Atmosphere production Download PDFInfo
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- US2473525A US2473525A US564541A US56454144A US2473525A US 2473525 A US2473525 A US 2473525A US 564541 A US564541 A US 564541A US 56454144 A US56454144 A US 56454144A US 2473525 A US2473525 A US 2473525A
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
- C21D1/74—Methods of treatment in inert gas, controlled atmosphere, vacuum or pulverulent material
- C21D1/76—Adjusting the composition of the atmosphere
- C21D1/763—Adjusting the composition of the atmosphere using a catalyst
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/14—Production of inert gas mixtures; Use of inert gases in general
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J38/00—Regeneration or reactivation of catalysts, in general
- B01J38/04—Gas or vapour treating; Treating by using liquids vaporisable upon contacting spent catalyst
- B01J38/12—Treating with free oxygen-containing gas
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J7/00—Apparatus for generating gases
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B3/00—Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
- C01B3/02—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
- C01B3/32—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air
- C01B3/34—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents
- C01B3/38—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents using catalysts
- C01B3/386—Catalytic partial combustion
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B3/00—Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
- C01B3/02—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
- C01B3/32—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air
- C01B3/34—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents
- C01B3/46—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents using discontinuously preheated non-moving solid materials, e.g. blast and run
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
- C01B2203/02—Processes for making hydrogen or synthesis gas
- C01B2203/025—Processes for making hydrogen or synthesis gas containing a partial oxidation step
- C01B2203/0261—Processes for making hydrogen or synthesis gas containing a partial oxidation step containing a catalytic partial oxidation step [CPO]
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
- C01B2203/08—Methods of heating or cooling
- C01B2203/0805—Methods of heating the process for making hydrogen or synthesis gas
- C01B2203/085—Methods of heating the process for making hydrogen or synthesis gas by electric heating
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
- C01B2203/10—Catalysts for performing the hydrogen forming reactions
- C01B2203/1041—Composition of the catalyst
- C01B2203/1047—Group VIII metal catalysts
- C01B2203/1052—Nickel or cobalt catalysts
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
- C01B2203/16—Controlling the process
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
- C01B2203/16—Controlling the process
- C01B2203/1628—Controlling the pressure
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
- C01B2203/16—Controlling the process
- C01B2203/169—Controlling the feed
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- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/584—Recycling of catalysts
Definitions
- Figure l is a view of circuits and apparatus illustrating one form of my invention.
- two supply-pipes 2 and i are respectively utilized to supply or convey, under suitable pressure, air and a carbonaceous fuel-gas; a balancing regulator 6 being used for maintaining the supply uniform.
- the pipes feed into a constant pressure device 8 which maintains a constant pressure in a connecting pipe ll! leading to a constant fiow device i2 which provides a constant flow of the supply-mixture of air and fuel-gas in an inlet pipe H! to a gasgenerator E6, so that a substantially constant output of product-gas is provided in an output pipe it from which the product-gas may be delivered to any place where it is needed or is to be further treated.
- a device responsive to the obstruction which deposited carbon introduces to the flow of gas through the reactionchamber I prefer to use a device responsive to the obstruction which deposited carbon introduces to the flow of gas through the reactionchamber.
- a pressure-operated switch-means 42 is provided responsive to the pressure-drop across the reaction-chamber.
- the switch-means 42 includes contacts 44 that close when the gas-pressure drop across the reactionchamber is over a set value indicating an excessive gas-flow restriction, and that open when it is below that value, indicating the removal of such ex cessive restriction.
- the solenoid 5E will be energized, cutting off the supply of fuel-gas, but only so long as the locking circuit switch it is closed while the switch M is closed. If the contacts M open before the detent it has reached the switch it, the timer motor will stop at a particular place, awaiting the next closure of the pressure-actuated switch-means &2. Accordingly, it requires an integrated'closure time of the contacts Ml of the switch-means t2, before the solenoid 40 is actuated. This may require several operations of the switch-means 42.
- a holding circuit 99 is provided for causing the timer motor 66' to go through one or more complete revolutions whenever the pressure-actuated switch-means 42 is actuated for simultaneously closing the contacts 44 and 44".
- This holding circuit includes a switch 9
- One revolution will be made when the switch-means t2 closes the contacts M" for a period less than the time of a revolution of the cams ill and 12'.
- the cam H! has a detent it which is adjusted to maintain the switch M in normally closed position when the timer motor stops so that the air shot for the reaction-chamber occurs immediately upon the closure of the pressure-actuated contacts M and M". Any other adjustment can obviously be provided.
- the detent 18' has passed the cooperating lug of the switch 14, the latter opens and the solenoid 40' deenergizes, restoring the fiow of fuel-gas through the fuel-gas supply-pipe.
- the solenoid 36' remains energized through contacts 44', allowing the relatively leaner mixture of fuel-gas and air to flow to the reaction-chamber immediately after the air shot stops.
- Independently timed air shots can be used where the carbon deposits quite densely at the inlet end, as it usually will with a gas-supply to the gas-generator which is entirely or mostly extremely rich.
- the time-controlled air shots alone will be supplied at regular intervals.
- the product-gas during this period of airoperation, will consist essentially of a mixture of nitrogen and carbon monoxide, without any hydrogen. This is another reason why the period of operation, with air only, should be short, so as not to greatly change the nature of the product-gas which is accumulated in the container (not shown) which is fed by the outlet-pipe iii of the gas-generator. It will be understood, of course, that this outlet-gas can be diverted to the atmosphere or to another container, if it should not be dseirable or permissible to mix it with the regular product-gas of the apparatus.
- catalyst in a predetermined direction, a mixture of a carbonaceous fuel-gas and air in an amount less than necessary to oxidize, to carbonmonoxide, the carbon content of the mixture so that additional free carbon will be slowly depositing within the pores of the catalyst; and before the deposited carbon clogs the-apparatus, forcingthrough said catalyst in said direction, instead of the first-mentioned mixture, another mixture of said gases having a relatively greater amount of air than said, first mixture for partially oxidizing the carbon-deposit within the pores of the catalyst; and periodically, for brief intervals, forcing through the catalyst in said direction, a gassupply composed substantially entirely of air for consuming carbon deposited at the gas-entrance end of the catalyst.
- a method for continuously producing a product-gas utilizable for a special atmosphere in a heat-treating furnace, by the reaction of air and a fuel-gas comprising hydrogen and carbon which method comprises a plurality of steps operating under a pro-arranged control, said steps comprising passing a gas-supply of the fuel-gas and air into a gas-porous heated catalyst in a predetermined direction, the fuel-gas and air being in amounts such that free carbon will be deposited in said catalyst, and product-gas produced, with the deposit being more dense at a gasinlet point in the catalyst than at other places therein, passing: a leaner gas-supply of the fuelgas and air into the catalyst, in said direction, for providing product-gas and for consuming deposited carbon in the catalyst beyond said gasinlet point, and passing, for a brief interval, a still leaner gas-supply into the catalyst for reacting more strongly with said dense carbon deposit.
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- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Combustion & Propulsion (AREA)
- Health & Medical Sciences (AREA)
- Materials Engineering (AREA)
- Inorganic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Thermal Sciences (AREA)
- Metallurgy (AREA)
- Mechanical Engineering (AREA)
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- Devices And Processes Conducted In The Presence Of Fluids And Solid Particles (AREA)
Description
June 21, 1949. J, oop 2,473,525
ATMOSPHERE PRODUCTION Filed Nov. 21, 1944 WITNESSES: INVENTQR ay/ John 6. H0 0p ATTORNEY Patented June 21, 1949 UNITED STATES PATENT OFFICE ATMOSPHERE PRODUCTION John G. Hoop, Forest Hills, Pa., assignor to Westinghouse Electric Corporation, East Pittsburgh, Pa., a corporation of Pennsylvania Application November 21, 1944, Serial No. 564,541
16 Claims. 1
My invention relates broadly to gas-reacting systems for producing a special gaseous atmosphere such as is used for enveloping metal undergoing a heat-treating process, the production of the atmosphere involving the reaction of a combustible fuel fluid, usually gaseous, and air in the presence of a heated catalyst for providing a product-gas utilizable, directly, or after further processing, for the special atmosphere.
The characteristics of the special atmosphere to be used in a metal heat-treating process are determined, to a large extent, by the physical and chemical properties of the articles which the atmosphere is to envelop, and the nature of the heat-treating process they are to undergo. However, from the standpoint of the supplier of gasreacting apparatus, it is desirable to provide a single apparatus which can provide a satisfactory product-gas with any of the more common fuelgases so that it can be used with a fuel-gas that is available more cheaply in one location, or with some other fluid fuel that might be more readily available at some other location.
It is also desirable to provide a means and a method in which the nature of the product-gas can be changed when it is produced from the reaction of a single fluid fuel and air. For example, air and methane can be reacted in a ratio of about 2% of air to 1 of methane for producing a product-gas which is admirably suited for use as a special neutral atmosphere for enveloping high carbon and alloy carbon steels for bright hardening without decarburization. By increasing this ratio to about 3 /2 to 1, the composition of the product-gas changes so that it is more suitable as a special neutral atmosphere in shortcycle hardening of medium carbon steels, without significant change in the carbon content of the steel.
In systems of the type described, significant amounts of carbon dioxide are generally undesirable in the enveloping atmosphere. Also practicable and economical considerations usually prevent feeding the input fuel-gas and air in a definite fixed ratio for continuously or automatically providing a product-gas of fixed composi tion. However, for most heat-treating processes, requiring a special atmosphere of a type described, the product-gas need not be of exactly the same composition at all times, but can vary through ranges which permit the use of a gas-generator system having a satisfactory control means. In general, a system provided with such a control means feeds a relatively rich mixture which causes free carbon to separate from the reacting gases and deposit in the catalystv bed. When the deposit becomes noticeable, as for example by the added restriction it interposes to gas-flow, the supply gas is made leaner for consuming carbon so as to remove the restriction. The controls are preferably such that some carbon is always left in the catalyst bed. The: copending. application of C. E. Peck and myself, Serial. No. 447,682, filed June 16, 1942, describes an automatic system having such a control means, and is especially useful in the production. of a product-gas from manufactured city gas: and air; my copending application Serial No..490,315,.filed June 10,1943, now abandoned, describes a modified form of such control means, and the instant application is a continuationsin-part and improvement thereof, which. provides a device of more general application in. industry.
The reaction of the fuel fluid and air, in systems of the type involved, is usually caused to take place while. the supply-gas passes through a heated gas-pervious porous catalyst contained in a reaction-chamber. The exact conditions and effects of the reaction of a. relatively rich gas-supply mixture which causes free carbon to separate from the gases and: deposit in the pores of the catalyst or of a" relatively lean gas-supply mixture which reacts with consumption of carbon, are not fully knownv sofar as I am aware. I have determined, however, that when. the gas.- supply is sufiiciently rich to cause. carbon to be deposited, the carbon does not deposit uniformly throughout the catalyst. The deposit appears to bemore dense at the entering side, with respect to the opposition it offers to gas-flow. When; a pure air shot is fed, along the. lines suggested in my aforesaid sole application, carbon in the pores of the catalyst is consumed, but the reac-- tion is highly exothermic and. can be permitted for a very brief time only. If an air shot is permitted' to continue too long, the catalyst may be overheated and deteriorate, so. that the sub-- stantially pure air shot scheme, although. utilizable in some cases, is not universally satisfactory as a scheme for preventing clogging of gas-generators which are; called upon to substantially continuously produce a satisfactory product-gas. On the other hand, the. alternate rich and lean supply-mixture, such as disclosed in the aforesaid jointv application, seems to consume the carbon primarily beyond the inlet portions of the catalyst. In some instances, it does not reduce the gas-flow restriction for intiating the control.
3 appreciably react with the carbon deposit in the entrance portion of the catalyst, where the carbon is most dense and is the primary cause of the gas-flow resistance. Accordingly, there are cases where the use of either control alone will not result in satisfactory operation of the gasgenerator system.
It is an object of my invention to overcome the disadvantages of the prior gas-generator systems.
It is another object of my invention to provide an apparatus and method by which a satisfactory product-gas can be consistently obtained from the reaction of any of the more common combustible fuel-gases with air.
It is another object of my invention to provide a gas-generator system of the type described in which the carbon deposited in the catalyst is more satisfactorily absorbed during the periods when a leaner gas-supply is supplied thereto.
Still another object of my invention is to provide a novel operating-cycle and control-system in combination with such gas-generators.
' In accordance with my present invention, I change the apparatuses and processes of the prior art embodiments so that the gas-supply to the reaction-chamber is changed in some orderly manner in which it is, at times, relatively so rich as to deposit carbon in the pores of the catalyst, so lean as to react mostly with the densely deposited carbon in the entrance portion of the catalyst, and relatively lean so as to slowly consume carbon primarily from the pores of the catalyst beyond the entrance portion. In a preferred embodiment, the most lean gas-supply consists of air which is supplied for very brief periods,
but sufiiciently long to provide satisfactory removal of carbon of the entrance portion of the catalyst bed without producing excessive heating.
Other objects, features, methods, combinations and innovations of my invention will be discernible from the accompanying drawing diagrammatically showing several preferred embodiments thereof. In the drawing, like numerals refer to similar parts of the embodiments illustrated in the figures of which:
Figure l is a view of circuits and apparatus illustrating one form of my invention; and
Fig. 2 is a similar view of another form.
As shown in the drawing, two supply-pipes 2 and i are respectively utilized to supply or convey, under suitable pressure, air and a carbonaceous fuel-gas; a balancing regulator 6 being used for maintaining the supply uniform. The pipes feed into a constant pressure device 8 which maintains a constant pressure in a connecting pipe ll! leading to a constant fiow device i2 which provides a constant flow of the supply-mixture of air and fuel-gas in an inlet pipe H! to a gasgenerator E6, so that a substantially constant output of product-gas is provided in an output pipe it from which the product-gas may be delivered to any place where it is needed or is to be further treated. The gas-generator comprises a reaction-chamber 2B in the form of a casing having a passage for the flowing gases, which is filled with a catalyst providing a porous catalyst bed 22. The catalyst may be nickel shot or balls of about' /4 inch diameter, or any other suitable catalyst. The casing is disposed in a heatinsulated furnace having any suitable heating means, exemplified by electrical resistor heaters 24, for heating the reaction-chamber to a degree necessary to sustain the reaction carried out in the reaction-chamber 20.
} Adjustable valves 26 and 28 are provided in the supply-pipes 2 and 4, respectively, for permitting an initial adjustment of the amounts of air and fuel-gas that can pass therethrough.
Bridging the valve 26 is piping 30 having an inlet on the inlet side of the valve 26 and an outlet at the outlet side of the same valve, at a point before the feed of the gas-supply to the constant pressure device 8. This branch piping 39 includes a manually-adjustable valve 32 for determining or setting the amount of air that can pass through the branch piping when it is otherwise unobstructed. However, another automatically-operable valve 34 is provided which is normally closed but which can be moved to fully open position upon energization of an operating means comprising a solenoid 36, for removing the barrier it normally presents to gas-flow.
A normally-open automatically-operable valve 38 is provided in the fuel-gas supply-pipe 4, before the inlet side of the valve 28. This valve 38 is moved to a closing position when an operating means comprising a solenoid 40 is energized. The restriction provided by the valve 38 in closing position is adjustably settable from a fully closed position in which no fuel-gas can flow through the length of the pipe 4, to any position ofiering a lesser barrier. When set to operate to fully closed position, the gas-supply to the reactionchamber will have a preponderance of oxidizing gas, consisting entirely of air, when the solenoid it is energized.
While any noticeable effect produced by the carbon deposited in the catalyst of the reactionchamber It can be used to control the solenoids 36 and 48, I prefer to use a device responsive to the obstruction which deposited carbon introduces to the flow of gas through the reactionchamber. To this end, a pressure-operated switch-means 42 is provided responsive to the pressure-drop across the reaction-chamber. The switch-means 42 includes contacts 44 that close when the gas-pressure drop across the reactionchamber is over a set value indicating an excessive gas-flow restriction, and that open when it is below that value, indicating the removal of such ex cessive restriction.
When the contacts M close, a circuit is completed from a conductor 4-6 of power line 58, through a conductor 55), through the closed contacts M to a junction point 52, from which two circuits branch.
A first of these circuits controls the air-flow through the branch piping 30 and comprises a normally-closed manually-operable switch "54, the solenoid 36, and a return conductor 55 which is connected to the other conductor 53 of the power line 48.
The other branch circuit which branches from th junction point 52 controls the flow of fuel gas through the supply-pipe 4, and comprises a normally-closed manually-operable switch 60 and a conductor 52 which leads to a junction point 64. From this junction point 54, a circuit is connected to a timer apparatus, indicated in its entirety by the reference numeral 65, and shown schematically as comprising an electrical timer motor 66 having one energizing terminal connected to the junction point 64 and its other energizing terminal to a conductor 68 connected to the power conductor 58 through a normally-closed manually-operable switch 69.
The timer motor 66 is preferably one which runs at a constant but adjustable speed, and drives a pair of cams l0 and 12 which control normally-open switches l5 and '16, through a '5 detent 18 on the cam Ill, and a detent 88 on the cam 12, respectively. The angular length of the detents can be adjustable.
Assume that the motor is rotating in the direction of the arrow shown. The cam 12 is so arranged that the detent 80 will close the switch 16 for completing a temporary locking circuit for the motor 66, through conductors 50 and 84, the switch Hi, and conductor 68. This locking circuit remains closed until the detent passes the cooperating lug of the switch 16.
The switch 14 is in an obvious circuit-branch from the junction point 64, this circuit including the conductor 8t and the solenoid 40 for the valve 38. If the motor 66 rotatessuificiently, the detent 88 will close the switch it, completing this circuit-branch so that the solenoid 40 will become energized if the motor holding circuit, including the conductor 84, is completed through the switch F6 to the junction point M, or if the contacts 44 are closed, thereby completing a circuit path from conductor 59 to the junction point 64.
It is desirable to have the rotation of the 'detent 80 time-related to the operation of the switch M by the detent 78 so as to have the switch it closed during the time that the switch 74 is closed, in order to prevent surge conditions, arising out of changes in the gas-flow, from interfering with smooth operation of the timer.
In the operation of the system shown in Fig. 1, it may be initially assumed that the gas-supply to the gas-generator is slightly over-ricl1, the pores of the catalyst in the reaction-chamber are being slowly filled with free carbon, the fuel-gas valve 38 open but adjusted so as to be operable to fully closed position, and the air valve 3-4 in the branch 3E closed. When the accumulation of carbon in the catalyst, under such an operating condition of the system, is suiiiciently great to cause the pressure-actuated switch-means 2 toclose its contacts M, the solenoid 36 is closed, opening the valve 34 and permitting additional air to flow to the constant pressure device 8, through the branch pipe 30, for changing to another operating condition of the system in which the ratio of the air to gas in the gas-supply is increased, depending on the position of switch 14. With the switch 74 open, so that the fuel-gas valve is open, the gassupply should be slightly too lean, with suflicient oxidizing power to slowly consume deposited carbon in the hot catalyst. Assuming that the contacts it remain closed until the detent 1-8 of the cam lll reaches and closes the switch 14, the solenoid t thereupon is energized for closing the fuel-gas valve 38, and again altering the operating condition of the system. The supply of fuel-gas is shut down and a preponderance of oxidizing gas, in this case in the form of substantially pure air, flows into the reactionchamber for a time-period determined by the time the solenoid remains energized.
The air-control solenoid 36 energizes immediately upon closure of the contacts 44 by the pressure-actuated switch-means 42 and remains energized when these contacts are closed. Energization of the air-control solenoid 36 Without energization of the fuel-gas-control solenoid 40 permits a relatively lean oxidizing mixture to flow through the reaction-chamber 20 for slowly consuming carbon, primarily in the part of the reaction-chamber appreciably beyond theinlet end. When the solenoid 4B is subsequently "power of the gas is greatly increased and carbon in the inlet portion of the catalyst is consumed more rapidly than elsewhere.
When the consumption of carbon has progressed to a suitable degree, the pressure-actuated switchmeans 42 restores to a position opening contacts l l.
Unless the switch T6 happens to be closed, opening of the contacts it causes the solenoid '36 and timer B5 to become deenergized, the air valve 35 to restore to its initial closed condition, the timer motor to stop in whatever position it is in, and the original rich supply-mixture to be restored.
If the switch it happens to be closed when contacts i l open, in the embodiment disclosed in which the switches 14 and 16 operate substantially together, the solenoid 5E) will be energized, cutting off the supply of fuel-gas, but only so long as the locking circuit switch it is closed while the switch M is closed. If the contacts M open before the detent it has reached the switch it, the timer motor will stop at a particular place, awaiting the next closure of the pressure-actuated switch-means &2. Accordingly, it requires an integrated'closure time of the contacts Ml of the switch-means t2, before the solenoid 40 is actuated. This may require several operations of the switch-means 42. To have a single operation of the switch i l during one revolution of the cam lEl, only a single detent equivalent to i8 is provided on the cam in, in which case the integrated closure time is substantially that of a complete revolution of the cam 19 by the timer motor. Accordingly, for each revolution of the cam it, gas-supply consisting of an air shot will be provided, either before the relatively lean gas-supply if the switch 1'6 is closed substantially simultaneously with the contacts it, or superseding it for a time if the switch M is closed later.
In Fig. 2, however, a holding circuit 99 is provided for causing the timer motor 66' to go through one or more complete revolutions whenever the pressure-actuated switch-means 42 is actuated for simultaneously closing the contacts 44 and 44". This holding circuit includes a switch 9| which is normally open when the motor 66 isstationary in a predetermined position, but completes a motor-energizing circuit in all other positions of the motor, in any well-known manner. One revolution will be made when the switch-means t2 closes the contacts M" for a period less than the time of a revolution of the cams ill and 12'. If the contacts 44 and 44" remain closed after the timer motor 66' has completed a single revolution, the timer will continue upon a second complete revolution and so on, stopping only after it completes the particular revolution in which the pressure-actuated switchmeans 42 releases or opens its contacts.
'Fig. 2 difiers from Fig. 1 also in the fact that the solenoid 3t is actuated only during closure of the contacts of the pressure-actuated switchmeans 42, while the solenoid 40' is actuated at least once for each closure of these contacts.
In Fig. 2, the cam H! has a detent it which is adjusted to maintain the switch M in normally closed position when the timer motor stops so that the air shot for the reaction-chamber occurs immediately upon the closure of the pressure-actuated contacts M and M". Any other adjustment can obviously be provided. After thedetent 18' has passed the cooperating lug of the switch 14, the latter opens and the solenoid 40' deenergizes, restoring the fiow of fuel-gas through the fuel-gas supply-pipe. In the meantime, if the pressure drop or differential across the reaction-chamber has not been decreased to the proper extent, the solenoid 36' remains energized through contacts 44', allowing the relatively leaner mixture of fuel-gas and air to flow to the reaction-chamber immediately after the air shot stops.
Apparatus in accordance with the foregoing is also useful for controlling the carbon pressure or potential of the gas, since numerous adjustments are possible.
If a high carbon pressure product-gas is desired at all times, the air shots may be made independent of the gas-pressure control system. Specifically, referring to Fig. 1, they can be made independent of the pressure-actuated switchmeans 42 by opening the normally-closed switch ,60 and closing a manually-operable normallyopen switch 92 paralleling the locking circuit switch 16. Under these connections, the timer motor 66 is continuously energized and, therefore, continuously rotates so as to periodically supply an air shot to the reaction-chamber while the supply of relatively leaner mixture remains under control of the pressure-actuated switchmeans 42. Independently timed air shots can be used where the carbon deposits quite densely at the inlet end, as it usually will with a gas-supply to the gas-generator which is entirely or mostly extremely rich. By opening the switch 54 also, the time-controlled air shots alone will be supplied at regular intervals.
If a medium or low value of carbon pressure is desired, as it might be for some heat-treating processes, air shots would not only be unnecessary but undesirable since the relatively rich gassupply would not be sufiiciently rich to cause appreciable carbon deposits even over extended periods of time. By leaving switches 60, 69, and 92 open, air shots are prevented.
With switches Gil, iii} and 92 open, and switch 54 closed, the system becomes substantially that shown in the aforesaid joint application of Peck and myself, insofar as the general sequence of control operations is concerned.
By leaving switches 54 and 92 open and switches 69 and 69 closed, the operation of the system becomes practically like that of my aforesaid sole application, except usually for the timing of the air shots and the adjustments of the proportions of air and gas in the gas-supply dur-- ing the different settings of the gas-flow determining or controlling devices.
Because of the variations in the kind of fuelgas used in practice, and in its pressure, composition, and other variables, it is diihcult to set forth exact conditions of operation for all applications. Generally, in the aggregate, for the more common uses of the apparatus, the rich carbondepositing mixture is on from periods of three minutes to three hours and more, and the lean carbon-consuming mixture from three minutes to one hour, approximately. Air shots persist for about fifteen seconds to as much as two minutes or more, every ten minutes to two hours, approximately. A specific example of a system utilizing this invention with a reaction-chamber slightly more than three feet long, having a capacity of one thousand cubic feet of productgas per minute, used a fuel-gas comprising a mixture of 60% coal gas and 40% water gas, the former having a composition in percentages of 2.9 CO2, 2.9 illuminants, .6 02, 14.4 C0, 25.1 CO2, 49.4 Hz and the balance N2; and the latter 4.5 CO2, 9.7 illuminants, .6 02, 31.1 C0, 15.7 CH4, 32.4 Hz, and the balance N2. Air and fuel-gas were reacted in volume ratios of 1 of air to 3 of fuel-gas for from fifteen to eighteen minutes and shifted to a ratio of 1:1 for about fifteen to twenty-two minutes in repeating cycles. Approximately one minute air shots were supplied every totalized fifteen minutes of relatively lean mixture flow. When the gas-supply ratio was 1:3, the product-gas had a dew point of 3 F. and a composition in percentages of 25.8 C0, .3 CO2, 1.4 CH4, 51.7 Hz, balance N2; and in a ratio of 1:1, the product-gas had a dew point several degrees higher and a composition in percentages of 28.2 C0, .2 C02, .8 CH4, 34.? H2, balance N2. For this operation, a fifteen-second air shot was required about every fifteen minutes of lean-mixture flow.
I have found, by tests, that the effect of substantially pure air is to react quickly with carbon, even in the entering section of the porcus catalyst 9. This is probably true because the reaction between air and carbon is exothermic, resulting in sufficient heating to carry on the reaction even in the absence of preheating of the air. In fact, the time during which the passage of air is permitted must be carefully limited to a short time-interval, so as to reduce the localized, excessive temperatures which may otherwise become suificiently high to be injurious to the equipment, if the rapid oxidation of the carbon were permitted to continue for any extended length of time.
The product-gas, during this period of airoperation, will consist essentially of a mixture of nitrogen and carbon monoxide, without any hydrogen. This is another reason why the period of operation, with air only, should be short, so as not to greatly change the nature of the product-gas which is accumulated in the container (not shown) which is fed by the outlet-pipe iii of the gas-generator. It will be understood, of course, that this outlet-gas can be diverted to the atmosphere or to another container, if it should not be dseirable or permissible to mix it with the regular product-gas of the apparatus.
While I have described my invention in forms which are now preferred, it is obvious that many modifications can be made therein and equivalent parts substituted for those symbolically and schematically shown. Thus, for example, although the devices 42 and 42 have been described as pressure responsive devices, the term, pressure responsive device, and similar expressions, include a device actuable otherwise than directly by pressure so long as it is responsive to, or reflects, pressure.
I claim as my invention:
1. A method of manipulating a gas-generating apparatus; said apparatus comprising a porous catalyst bed having some carbon deposited within its pores, a gas-supply means for forcing a mixture of two gases through said catalyst, richnessregulating means for varying the proportions of the gases in said mixture, and means for adding heat to said mixture while it is undergoing a reaction within the pores of said catalyst; said method comprising periodically forcing, through said. catalyst, in a predetermined direction, a mixture of a carbonaceous fuel-gas and air in an amount less than necessary to oxidize, to carbonmonoxide, the carbon content of the mixture so that additional free carbon will be slowly depositing within the pores of the catalyst; and before the deposited carbon clogs the-apparatus, forcingthrough said catalyst in said direction, instead of the first-mentioned mixture, another mixture of said gases having a relatively greater amount of air than said, first mixture for partially oxidizing the carbon-deposit within the pores of the catalyst; and periodically, for brief intervals, forcing through the catalyst in said direction, a gassupply composed substantially entirely of air for consuming carbon deposited at the gas-entrance end of the catalyst.
2. A method for continuously producing a product-gas utilizable for a special atmosphere in a heat-treating furnace, by the reaction of air and a fuel-gas comprising hydrogen and carbon, which method comprises a plurality of steps operating under a pro-arranged control, said steps comprising passing a gas-supply of the fuel-gas and air into a gas-porous heated catalyst in a predetermined direction, the fuel-gas and air being in amounts such that free carbon will be deposited in said catalyst, and product-gas produced, with the deposit being more dense at a gasinlet point in the catalyst than at other places therein, passing: a leaner gas-supply of the fuelgas and air into the catalyst, in said direction, for providing product-gas and for consuming deposited carbon in the catalyst beyond said gasinlet point, and passing, for a brief interval, a still leaner gas-supply into the catalyst for reacting more strongly with said dense carbon deposit.
3. A method for continuously producing a product-gas of a type described, utilizable for a special atmosphere in a heat-treating furnace, by the reaction of air and a combustible fuel gas comprising hydrogen and carbon, which method comprises passing, in a predetermined direction, a mixture of a fuel gas and air through a gas pervious heated catalyst bed in amounts such that free carbon will be deposited in said catalyst bed and product-gas produced, the deposited carbon restricting the flow of the gas mixture through the catalyst bed, repeatedly interrupting the flow of the gas mixture, and during some interruptions supplying air to said catalyst bed, the last said interruptions being for brief periods for consuming deposited carbon at the gas-entrance end of the catalyst bed, and during remaining interruptions supplying a mixture of fuel gas and air, the last said mixture being more oxidizing than the first said mixture for consuming carbon in the catalyst bed, and continually withdrawing said product-gas from said catalyst bed.
4. A gas-generator comprising, in combination, an oxidizing-gas supply-means including an oxidizing-gas conduit for supplying an oxidizing gas, a fuel-gas supply-means including a fuel-gas conduit for supplying a carbonaceous fuelgas, a Valve in said fuel-gas conduit, means for mixing the gases from said conduits, a reaction-chamber having a porous catalyst filling, an inlet-conduit for supplying said mixture to said reactionchamber, an outlet-conduit for said reactionchamber, means for heating said reaction-chamber, means for maintaining a substantially constant rate of gas-flow through said reactionchamber, a pressure-responsive means, including a conduit-connection to said inlet-conduit, for responding to changes in the resistance togasfiow through said reaction-chamber, and means operatively connected and responsive to said pressure-responsive means for operating said valve in the fuel-gas conduit.
5. A gas-generator comprising, in combination, an oxidizing-gas supply-means including an oxidizing-gas conduit for'supplying an oxidizing gas, a fuehgas supply-means including a fuel-gas conduit for supplying a carbonaceous fuel-gas, means for mixing the gases from said conduits, a reaction-chamber having a porous catalytic filling, an inlet-conduit for supplying said mixture to said reaction-chamber, an outlet-conduit for said reaction-chamber, means for heating said reactionchamber, means for maintaining a substantially constant rate of gas-flow through said reactionchamber, a pressure-responsive means, including a conduit-connection to said inlet-conduit, for responding to changes in the resistance to gas-fiow through said reaction-chamber, and means operatively connected and responsive to said pressureresponsive means, for substantially shutting ofi? the fiow of gas through said fuel-gas conduit.
6. The invention as defined in claim i, in combination with timer-means, responsive to said predetermined pressure-response, for thereafter maintaining said valve-operation for a predetermined fixed period of time.
7. The invention as defined in claim 5, in combination with timer-means, responsive to said predetermined pressure-response, for thereafter keeping the fiow of gas through the fuel-gas conduit shut off for a predetermined short fixed period of time.
8. The invention as defined in claim 4, in combination with means associated with the oxidizing-gas and fuel-gas conduits for varying the relative proportions of the oxidizing gas and the fuel-gas delivered therefrom.
9'. The invention as defined in claim 5, in combination with means associated with the oxidizing-gas and fuel-gas conduits for varying the relative proportions of the oxidizing gas and the fuel-gas delivered. therefrom.
10. A gas-generator comprising, in combination, an oxidizing-gas supply-means including an oxidizing-gas conduit comprising a valve therein, for supplying an oxidizing gas, a fuel-gas supplymeans including a fuel-gas conduit for supplying a carbonaceous fuel-gas, a valve in said fuel-gas conduit, means for mixing the gases from said conduits, a reaction-chamber having a porous catalytic filling, an inlet-conduit for supplying said mixture to said reaction-chamber, an outletconduit for said reaction-chamber, means for heating said reaction-chamber, a device responsive to pressure of gas in said inlet-conduit, means operated by said device for operating said oxidizing-gas valve, an electrical mechanism energizable for operating said fuel gas valve, a timer, a circuit including said electrical mechanism and a switch, and operable means for opening and closing said switch, the last said means being operated by said timer.
11. A system for supplying a protective atmosphere to heat-treating furnaces, comprising a reaction-chamber adapted to contain a catalyst promoting the oxidation of a fuel gas, an outlet conduit from said reaction chamber, an inlet conduit to said reaction-chamber, a first branched conduit thereto for the supply of fuel gas, a second branched conduit thereto for the supply of oxygen to mix with said fuel gas in said inlet conduit, a first valve means in said second branched conduit, a supply line for air connected to said inlet conduit between said first valve means and said reaction chamber, an automatically operated valve in said supply line, means connected to said inlet conduit and responsive to changes in pressure in said inlet conduit for operating said valve, an automatically operated valve in said fuel gas branch conduit, means arranged to close said fuel gas valve momentarily likewise actuated by said means responsive to changes in pressure, and effective during an extended period of opening of said first valve.
12. A gas-generator comprising, in combination, an oxidizing-gas supply-means including an oxidizing-gas conduit for supplying an oxidizing gas, a fuel-gas supply means including a fuelgas conduit for supplyin a carbonaceous fuel gas, a valve in said fuel-gas conduit, means for mixing the gases from said conduits, a reaction chamber having a porous catalyst filling, an inletconduit for supplying said mixture to said reaction-chamber, an outlet-conduit for said reaction-chamber, means for heating said reactionchamber, a pressure-responsive means, including a conduit-connection to said inlet-conduit, for responding to changes in the resistance to gasfiow through said reaction-chamber, and means operatively connected and responsive to said pressure-responsive means for operating said valve in the fuel-gas conduit.
13. A gas-generator comprising, in combination, an oxidizing-gas supply-means including an oxidizing-gas conduit for supplying an oxidizing gas, a fuel-gas supply-means including a fuelgas conduit for supplying a carbonaceous fuelgas, means for mixing the gases from said conduits, a reaction-chamber having a porous catalytic filling, an inlet-conduit for supplying said mixture to said reaction-chamber, an outlet-conduit for said reaction-chamber, means for heating said reaction-chamber, a pressure-responsive means, including a conduit-connection to said inlet-conduit, for responding to changes in the resistance to gas-flow through said reaction-chamher, and means operatively connected and responsive to said pressure-responsive means, for substantially shutting off the fiow of gas through said fuel-gas conduit.
14. The invention as defined in claim 12, in combination with timer-means, responsive to said predetermined pressure-response, for thereafter maintaining said valve-operation for a predetermined fixed period of time.
The invention as defined in claim 13, in combination with timer-means, responsive to said predetermined pressure-response, for thereafter keeping the flow of gas through the fuel-gas conduit shut off for a predetermined short fixed period of time.
16. A system for supplying a protective atmosphere to heat-treating furnaces, comprising a reactionmchamber adapted to contain a catalyst pro-- muting the oxidation of a fuel-gas, an outlet conduit from said reaction chamber, an inlet conduit to said reaction-chamber, a first branched conduit thereto for the supply of fuel gas, a second branched conduit thereto for the supply of oxygen to mix with said fuel gas in said inlet conduit, a first valve means in said second branched conduit, a supply line for air connected to said inlet conduit between said first valve means and said reaction chamber, an automatically operated valve in said supply line, means connected to said inlet conduit and responsive to changes in pressure in said inlet conduit for operating said valve, and a timer means arranged to actuate said automatically operated valve in the fuel gas branch conduit to close same for a predetermined short fixed period of time.
JOHN G. HOOP.
REFERENCES CITED The following referenjces are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 40 1,770,563 Wannebo July 15, 1930 1,979,820 Bowling Nov. 6, 1934 2,047,499 Towne July 14, 1936 2,301,812 Rentschler et al. Nov. 10, 1942
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US564541A US2473525A (en) | 1944-11-21 | 1944-11-21 | Atmosphere production |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US564541A US2473525A (en) | 1944-11-21 | 1944-11-21 | Atmosphere production |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2473525A true US2473525A (en) | 1949-06-21 |
Family
ID=24254895
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US564541A Expired - Lifetime US2473525A (en) | 1944-11-21 | 1944-11-21 | Atmosphere production |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2473525A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2753170A (en) * | 1951-11-09 | 1956-07-03 | Metallurg Processes Co | Radiantly heated controlled atmosphere furnace |
| US2873173A (en) * | 1955-04-08 | 1959-02-10 | Sunbeam Corp | Endothermic gas generator |
| DE1148246B (en) * | 1954-06-05 | 1963-05-09 | Bataafsche Petroleum | Process for the controlled production of gas mixtures by reaction of gaseous hydrocarbons and a generator to carry out the process |
| WO2008053006A1 (en) * | 2006-10-31 | 2008-05-08 | Shell Internationale Research Maatschappij B.V. | Process for the production of hydrogen and the use thereof and a process for the operation of a internal combustion engine |
| WO2008053007A1 (en) * | 2006-10-31 | 2008-05-08 | Shell Internationale Research Maatschappij B.V. | Process for the production of hydrogen |
| EP2441731A1 (en) * | 2010-10-14 | 2012-04-18 | Honda Motor Co., Ltd. | In-situ coke removal in a catalytic partial oxidation process |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1770563A (en) * | 1923-09-11 | 1930-07-15 | Wannebo Kristian Nicolaus | Process of making oil gas |
| US1979820A (en) * | 1932-06-02 | 1934-11-06 | Electric Furnace Co | Heat treatment |
| US2047499A (en) * | 1931-08-19 | 1936-07-14 | Texas Co | Treatment of hydrocarbon gases |
| US2301812A (en) * | 1939-09-26 | 1942-11-10 | William J Wesseler | Method for producing and using nonoxidizing gases |
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- 1944-11-21 US US564541A patent/US2473525A/en not_active Expired - Lifetime
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1770563A (en) * | 1923-09-11 | 1930-07-15 | Wannebo Kristian Nicolaus | Process of making oil gas |
| US2047499A (en) * | 1931-08-19 | 1936-07-14 | Texas Co | Treatment of hydrocarbon gases |
| US1979820A (en) * | 1932-06-02 | 1934-11-06 | Electric Furnace Co | Heat treatment |
| US2301812A (en) * | 1939-09-26 | 1942-11-10 | William J Wesseler | Method for producing and using nonoxidizing gases |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2753170A (en) * | 1951-11-09 | 1956-07-03 | Metallurg Processes Co | Radiantly heated controlled atmosphere furnace |
| DE1148246B (en) * | 1954-06-05 | 1963-05-09 | Bataafsche Petroleum | Process for the controlled production of gas mixtures by reaction of gaseous hydrocarbons and a generator to carry out the process |
| US2873173A (en) * | 1955-04-08 | 1959-02-10 | Sunbeam Corp | Endothermic gas generator |
| WO2008053006A1 (en) * | 2006-10-31 | 2008-05-08 | Shell Internationale Research Maatschappij B.V. | Process for the production of hydrogen and the use thereof and a process for the operation of a internal combustion engine |
| WO2008053007A1 (en) * | 2006-10-31 | 2008-05-08 | Shell Internationale Research Maatschappij B.V. | Process for the production of hydrogen |
| US20100061921A1 (en) * | 2006-10-31 | 2010-03-11 | Haroldus Adrianus Johannes Van Dijk | Process for the production of hydrogen |
| US7998456B2 (en) | 2006-10-31 | 2011-08-16 | Shell Oil Company | Process for the production of hydrogen |
| EP2441731A1 (en) * | 2010-10-14 | 2012-04-18 | Honda Motor Co., Ltd. | In-situ coke removal in a catalytic partial oxidation process |
| US8784515B2 (en) | 2010-10-14 | 2014-07-22 | Precision Combustion, Inc. | In-situ coke removal |
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