US2281562A - Fuel gas production - Google Patents

Fuel gas production Download PDF

Info

Publication number
US2281562A
US2281562A US309504A US30950439A US2281562A US 2281562 A US2281562 A US 2281562A US 309504 A US309504 A US 309504A US 30950439 A US30950439 A US 30950439A US 2281562 A US2281562 A US 2281562A
Authority
US
United States
Prior art keywords
zone
incandescent
gas
distillation
coal
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US309504A
Inventor
Marvin W Ditto
William P Torrington
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
EMULSIONS PROCESS Corp
Original Assignee
EMULSIONS PROCESS CORP
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by EMULSIONS PROCESS CORP filed Critical EMULSIONS PROCESS CORP
Priority to US309504A priority Critical patent/US2281562A/en
Application granted granted Critical
Publication of US2281562A publication Critical patent/US2281562A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J3/00Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
    • C10J3/02Fixed-bed gasification of lump fuel
    • C10J3/06Continuous processes
    • C10J3/08Continuous processes with ash-removal in liquid state

Definitions

  • This "invention relates to the production of gas and more -particularly to the production of combustible gas such as used in metallurgical plants for heating purposes in open hearth furnaces, soaking pits, etc.
  • One-oi the objects of the invention is to pro- Slagging type producers cause of the high demand for heat made upon the incandescent zone, as the steam'causes rapid cooling and therefore retardation or cessation "of the 'slagging.
  • an emulsified liquid fuel is injected into .the'incandescent zone of the producer, suchfuel having sufficient water incorporated therein to supply the oxygen-hydrogendemand when combined with the steam used for-atomization. Due to the heatgenerated by the combustion of the emulsified fuel, we can meet the extra thermal demand necessary for the reaction of steam with the incandescent charge.
  • Fig. l isa vertical sectional view partly in elevation of a'gas producer in accordance with our invention.
  • Fig. 2 is a side elevation of an apparatus employed in manufacturing and preheating an emulsified liquid fuel, which is utilized in the producer.
  • coal 'or other suitable solid carbonaceous material, from which gases are to be :obtained is
  • the producer itself consists of a suitable steel shell 2 having a refractory lining 3 and an upper gas outlet t. Conventional poke holes 5 are arranged in the shell and lining at various elevations.
  • the producer hasa Bosch angle similar to a blast furnace and behind which there are the Bosch coolers 6. Water-cooled tuyres '1 are radially disposed around the stack or tower below the Bosch angle to accommodate nozzles 8 which receiveair under pressure from a bustle pipe 9.
  • H3 designates a steam manifold and I I an emulsified fuel manifold.
  • l2 indicates a steam fuel mixing'valveand l3 a'fuel nozzle extending from 'each'mixing valve into one of the air nozzles.
  • 'Valved tubes Illa convey steam'fromthe "manifold I ii to the mixing valves, and valved tubes I to H convey the emulsified fuel from the manifold H to such valves.
  • I4 designates a-slag crucible at the bottom of the stack; IS a slag tap-hole;'and l6 anysuitable slagidisposal means.
  • l1 designates an emulsified fuel heaterirom which the preheated fuel is conducted through a pipe lla. to the manifold l I.
  • l9 indicates a proportioning pump preferably at the type disclosed in the M. W. Ditto patent application'Serial No. 230,480, filed September 17, 1938, as such pump is capable of simultaneously pumping-water and oil and permitting the proportion of water to oil to be varied at any time,
  • Water is introduced into one end of the pump through a pipe 25 and is forced from the latter under superatmosphericpressure through a pipe 2
  • Residual tar or any other suitable fuel oil is introduced into the opposite'end of the pump through a pipe 22 and .is forced under pressure by the pump through a pipe 23 into the emulsification mill.
  • the mill acts to finely disperse the Water in the oil, and the resulting emulsion passes under pressure through a pipe 24 into the heater H.
  • the latter is of the heat exchange type and it, as well as the jacket of the dispersion mill, may be heated by steam introduced through a pipe 25 and discharged through a conduit 28.
  • Our producer is a refractory'lined cylindrical structure approximately 25 feet in height, the bottom portion of which 'isa dolomite lined slag crucible. Just above this crucible, which is approximately 3 feet in depth, are a series of tuyeres and above this there is a slight Bosch angle similar to a blast furnace, to compensate for the reduction in volume of the coke after the coal has been carbonized. This oxidation zone, which is approximately 4 feet in height, is water cooled. Above this the furnace structure is straight and is equipped at the top with an automatic coal feeder. The gas off-take is situated at the top and side of the furnace structure.
  • Emulsified tar containing from 25 to 65% of water is introduced at the rate of from 10 to 100 gallons per ton of coal charged, depending on the amount of tar or fuel oil available and the desired calorific value of the gas.
  • coal or any suitable carbonaceous material is introduced into the top of the producer, and forms a column within the stack, the column being burned from the bottom up.
  • the material within the stack will form superposed zones which may be referred to as the slag zone, combustion and melting zone, oxidation zone, reduction zone and distillation zone, the last-mentioned zone being, of course, at the top of the column.
  • the combustion zone is in incandescent condition
  • hydrocarbon liquid and water in suitable proportions are forced by the pump 1 9 into the steam jacketed emulsifying mill l8 where a fine dispersion of the water in the oil takes place.
  • the emulsion from the mill is passed through the heater IT at a pressure of approximately 200 pounds per square inch, and at the time it leaves the heater. it is at a temperature of about 260 F.
  • the preheated emulsion is conducted from the heater through the manifold II which conducts it to the tubes Ha, leading to the various mixing valves l2 which are distributed around the producer.
  • the emulsion is thoroughly mixed with high pressure steam and discharges with the same through the nozzles l3 which introduce atomized emulsion into the blast air in the nozzles 8.
  • Sufiicient air is introduced through the tuyeres to gasify approximately 200 pounds of coal per square foot of hearth area.
  • the amount of emulsified fuel or tar employed varies from 10 to 100 gallons per ton of coal gasifled.
  • the emulsion introduced with a large excess of air, combined with the high temperature of the combustion zone, causes rapid flame propagation, resulting in very rapid heat release. This tends to maintain an extremely high temperature in the combustion zone at the place where fusion of the ash takes place, and consequently the slag present in'the crucible I4 is maintained in a liquid condition.
  • the operation of the unit is so balanced that sufiicient water vapor is derived from the water of the emulsion and the atomizing steam to amount to practically 0.4 to 1.5 pounds of water vapor per pound of coal gasified.
  • a slagging ash producer can be operated to advantage on coals having low fusion ash as they tend to limit the rate at which ordinary producers can be operated but the objection to the operation of the slagging ash producers has been the low calorific value of the gas as a result of the operation without water vapor, combined with the fact that fluxing material must be added to the coal in order to cause efficient slagging of the ash.
  • our method of operation we eliminate these objections while also producing producer gas of higher calorific value. Besides we produced such gas while utilizing residual tar or other liquid hydrocarbons as fuel.
  • Fuel gas is normally formed by the passage of a stream of steam and air through the thick bed of coal; primarily the reactions take place in three steps.
  • the rate at which the coal maybe gaslfied ranges from 8.9 to about 100 pounds of coal per square foot of grate per hour. This is'determined by the fusion temperature of the ash in the coal as the producers are only equipped to dispose of unfused ash. Fusing of ash causes extreme difficulty from clinker formation. Fuel bed depth varies from 3.75 to 7 feet and pounds of steam per pound of coal varies from .28 to 1.57. Theoretically it would be best to use the amount of steam that would give the maximum efficiency of decomposition and therefore a minimum of dilution of the resulting gas with undecomposed steam. Under present operating conditions this cannot 'be done practically.
  • These combined products of combustion highly preheated are then carried into primary reduction zone where due to the high temperature and the absence of oxygen reduction of the CO2 and water vapor occur. It is generally supposed that approximately of the uncombined hydrogen also reacts with the carbon to form CH4.
  • These hot gases then pass through the secondary reduction zone where some further reduction occurs and are then passed through a thick bed of coal so as to cause distillation of the volatiles (if present) and a reduction in the sensible heat of the gases.
  • bent charge of fresh substantially solid carbonaceous material arranged in superposed oxidation, reduction and distillation zone injecting a waterin-fuel oil emulsion in atomized condition into the incandescent body and burning the emulsion therein, passing hot gases from the incandescent body upwardly through said super-incumbent charge and thereby subjecting carbonaceous material of the charge to distillation and partial combustion, and discharging the resulting gases from the distillation zone, the amount of air introduced into the incandescent body being suflicient to cause the ash discharged to flow therefrom in liquid condition.

Description

May'5, 1942. M. w. DITTO ETAL FUEL GAS PRODUCTION Filed Dec. 15, 1939 2 Sheets-Sheet l o'n Fuel w 5 m h 6 OLZ EDauZfgEra &
W J? Tor/'0' .May 5, 1942.
M. W. DITTO ETAL 2,281,562
FUEL GAS PRODUCTION Filed Dec. 15, 1939 2 SheetsSheet 2 glrwcmf w M W 3,0220, W]? Tori 622 5020,
Patented May 5, 1942 UNlTED STATS FUEL GAS PRODUCTION Marvin W. Ditto and William P. Torrington,
New York, N. -Y., assignors to Emulsions Process Corporation, New "York, N. .Y., a corporation of Delaware Application December 15, 1939, Serial No. 309,504
13 Claims.
This "invention relates to the production of gas and more -particularly to the production of combustible gas such as used in metallurgical plants for heating purposes in open hearth furnaces, soaking pits, etc.
One-oi the objects of the invention is to pro- Slagging type producers cause of the high demand for heat made upon the incandescent zone, as the steam'causes rapid cooling and therefore retardation or cessation "of the 'slagging. In accordance with our invention an emulsified liquid fuel is injected into .the'incandescent zone of the producer, suchfuel having sufficient water incorporated therein to supply the oxygen-hydrogendemand when combined with the steam used for-atomization. Due to the heatgenerated by the combustion of the emulsified fuel, we can meet the extra thermal demand necessary for the reaction of steam with the incandescent charge. This permits a higher rateof gasification of the coal and the use of any-other suitable solid carbonaceous material such as coke, anthracite coaL'bituminous or subbituminous coal, as the method operates regardless of thefusion point of the ash derived from such material because sufficient heat is gen- -erated to liquefy the ash and to allow the-ash and clinker-forming material to be discharged as liquid slag. It will therefore be understood that it is another object of the invention to supply a method by which higher calorific gas ;ducers by utilizing residual tar or its equivalent incombination with solid carbonaceous material.
Other objects of the invention will appear from'the'following description taken in connection with the accompanying drawings in which:
Fig. l isa vertical sectional view partly in elevation of a'gas producer in accordance with our invention.
Fig. 2 is a side elevation of an apparatus employed in manufacturing and preheating an emulsified liquid fuel, which is utilized in the producer.
Such apparatus will be described in conjunction with the method of operating the same. The
coal 'or other suitable solid carbonaceous material, from which gases are to be :obtained, is
introduced into the upper end of the producer through a charging apparatus l and a conventional seal and charging bell. The producer itself consists of a suitable steel shell 2 having a refractory lining 3 and an upper gas outlet t. Conventional poke holes 5 are arranged in the shell and lining at various elevations. The producer hasa Bosch angle similar to a blast furnace and behind which there are the Bosch coolers 6. Water-cooled tuyres '1 are radially disposed around the stack or tower below the Bosch angle to accommodate nozzles 8 which receiveair under pressure from a bustle pipe 9.
H3 designates a steam manifold and I I an emulsified fuel manifold. l2 indicates a steam fuel mixing'valveand l3 a'fuel nozzle extending from 'each'mixing valve into one of the air nozzles. 'Valved tubes Illa convey steam'fromthe "manifold I ii to the mixing valves, and valved tubes I to H convey the emulsified fuel from the manifold H to such valves. I4 designates a-slag crucible at the bottom of the stack; IS a slag tap-hole;'and l6 anysuitable slagidisposal means.
Referring now to Fig. 2, l1 designates an emulsified fuel heaterirom which the preheated fuel is conducted through a pipe lla. to the manifold l I.
18 designates an emulsification mill preferably of the type disclosed in the patent to M. W. Ditto, No. 2,169,338 or No. 2,169,339.
l9 indicates a proportioning pump preferably at the type disclosed in the M. W. Ditto patent application'Serial No. 230,480, filed September 17, 1938, as such pump is capable of simultaneously pumping-water and oil and permitting the proportion of water to oil to be varied at any time,
even during the operation of the pump. Water is introduced into one end of the pump through a pipe 25 and is forced from the latter under superatmosphericpressure through a pipe 2| into the emulsification mill. Residual tar or any other suitable fuel oil is introduced into the opposite'end of the pump through a pipe 22 and .is forced under pressure by the pump through a pipe 23 into the emulsification mill. The mill acts to finely disperse the Water in the oil, and the resulting emulsion passes under pressure through a pipe 24 into the heater H. The latter is of the heat exchange type and it, as well as the jacket of the dispersion mill, may be heated by steam introduced through a pipe 25 and discharged through a conduit 28.
Our producer is a refractory'lined cylindrical structure approximately 25 feet in height, the bottom portion of which 'isa dolomite lined slag crucible. Just above this crucible, which is approximately 3 feet in depth, are a series of tuyeres and above this there is a slight Bosch angle similar to a blast furnace, to compensate for the reduction in volume of the coke after the coal has been carbonized. This oxidation zone, which is approximately 4 feet in height, is water cooled. Above this the furnace structure is straight and is equipped at the top with an automatic coal feeder. The gas off-take is situated at the top and side of the furnace structure. introduced through tuyeres at pressures ranging from 5 to pounds per square inch and in the necessary quantity in order to gasifyup to 200 pounds of coal per square foot of furnace area, at the Bosch line, per hour. The emulsion is introduced through the tuyres by means of special steam atomizing burners supplying enough steam beside the water contained in the emulsion to react with the carbon in the coal. Emulsified tar containing from 25 to 65% of water is introduced at the rate of from 10 to 100 gallons per ton of coal charged, depending on the amount of tar or fuel oil available and the desired calorific value of the gas.
In operation, coal or any suitable carbonaceous material is introduced into the top of the producer, and forms a column within the stack, the column being burned from the bottom up. After ignition is started in any suitable way, the material within the stack will form superposed zones which may be referred to as the slag zone, combustion and melting zone, oxidation zone, reduction zone and distillation zone, the last-mentioned zone being, of course, at the top of the column. While the. combustion zone is in incandescent condition, hydrocarbon liquid and water in suitable proportions are forced by the pump 1 9 into the steam jacketed emulsifying mill l8 where a fine dispersion of the water in the oil takes place. The emulsion from the mill is passed through the heater IT at a pressure of approximately 200 pounds per square inch, and at the time it leaves the heater. it is at a temperature of about 260 F. The preheated emulsion is conducted from the heater through the manifold II which conducts it to the tubes Ha, leading to the various mixing valves l2 which are distributed around the producer. In the mixing valves, the emulsion is thoroughly mixed with high pressure steam and discharges with the same through the nozzles l3 which introduce atomized emulsion into the blast air in the nozzles 8. Sufiicient air is introduced through the tuyeres to gasify approximately 200 pounds of coal per square foot of hearth area.
The amount of emulsified fuel or tar employed varies from 10 to 100 gallons per ton of coal gasifled. The air introduced through the tuyeres into the incandescent bed of devolatized coal, rapidly raises the temperature within the combustion zone of the stack, as the oxygen in the air combines with the carbon of the fuel to form C02. The emulsion introduced with a large excess of air, combined with the high temperature of the combustion zone, causes rapid flame propagation, resulting in very rapid heat release. This tends to maintain an extremely high temperature in the combustion zone at the place where fusion of the ash takes place, and consequently the slag present in'the crucible I4 is maintained in a liquid condition. Obviously the water and steam are highly superheated both from the combustion of the emulsion and the rapid oxidation of the carbon of the charge by The air is the air. The gaseous products .of combustion and the water vapor pass up through the column of fuel until all the oxygen has reacted to form 002. As soon as there is no free oxygen present, reduction of 0 plus H2O to CO plus H2 starts, and the reaction of C plus 002 to 2C0 takes place. Above the reduction zone, the high sensible heat of the gases causes distillation and partial carbonization of green coal in the absence of air, and the gaseous products of the distillation and partial decomposition mix with the rising gases to form the final gas which passes off through the discharge conduit 4.
The operation of the unit is so balanced that sufiicient water vapor is derived from the water of the emulsion and the atomizing steam to amount to practically 0.4 to 1.5 pounds of water vapor per pound of coal gasified. This results in the production of gas having a higher calorific value with lower nitrogen dilution, because the sensible heat created within the producer is utilized through the endothermic reaction of the decomposition of the water vapor and the reduction of the CO2 from the combustion of the emulsion to form CO. The decomposition of the water vapor takes place more efficiently than in ordinary producer practice because of the fact that the high rate of gasification results in high combustion temperatures plu the fact that combustion of the emulsion is so balanced to release sufficient heat that the endothermic demand to decompose the water vapor does not cool the ash, at the slag line, below its fusion point. i
There are a number of grateless gas producers nowin existence. In general they resemble a small blast furnace. As the air is introduced into such producers at relatively high pressures,
very high gasification rates are possible. The rapid combustion rate makes it possible to fuse the ash, though ordinarily some fiuxing material is introduced with the coal, such as blast furnace slag, sand, lime or the like. The gas produced by such grateless producers contains essentially CO and N2 and is of low calorific value due to the nitrogen dilution, as it has not been found practical to use steam or Water vapor with the blast air due to the fact that the high endothermic demand to decompose the water would interfere with the slagging of the ash.
It is recognized that a slagging ash producer can be operated to advantage on coals having low fusion ash as they tend to limit the rate at which ordinary producers can be operated but the objection to the operation of the slagging ash producers has been the low calorific value of the gas as a result of the operation without water vapor, combined with the fact that fluxing material must be added to the coal in order to cause efficient slagging of the ash. By our method of operation we eliminate these objections while also producing producer gas of higher calorific value. Besides we produced such gas while utilizing residual tar or other liquid hydrocarbons as fuel.
We have found in practice that the ignitibility and combustibility of emulsified fuel oils or tars even when saturated with as high as 65% water, is suitable for our purposes, because a sufficient quantity of air can be introduced into the prousing apparatus which requires operating temperatures below the fusion point of the ash.
Most gas producers used in the United States today are of the pre-fusion type with grates so arranged that the ash can be eliminated in dry unfused condition. Such producers are limited to very low rates of gaslfication per square foot of hearth area. Besides they necessitate careful selection of coal to be used so that proper fusion temperatures of ash do not throw the operating reactions out of gear. In pro-fusion type producers, both air and steam are used, the steam acting as gas making material and at the same time holding the temperature of the ash below the fusion point. Obviously our method also eliminates the objections to prefusion type pro- 1 ducers.
Byour procedure it is possible to produce a gas of higher calorific value containing illuminates, hydrocarbons, hydrogen and carbon monoxide, in which the ratio of nitrogen to the combustible matter contained in the gas is lower than the ratio contained in producer gas obtained by other slagging type producers. I
From the foregoing it is believed that our method of producing gas may be readily understood but by way of recapitulation, and for further disclosure we make the following statement.
The purposes of our method of operation are three in number.
1. Making it possible to operate gas producers with coal with low fusion ash at extremely high rates; the ash being tapped out as slag, sufiicient temperature being maintained in the thermal de composition chamber to maintain the ash in a liquid condition.
-2. The utilization of heavy gas-tars or other residue hydrocarbons in the producer to act as an enriching agent by converting this material into a fixed gas by high temperature thermal decomposition; reacting with water vapor and then the reduction of these products of combustion into carbon monoxide, hydrogen and other hydrocarbon gases.
3. Owing to the fact that the oxidation zone will operate at very high temperatures due to 'both the rapid rate of oxidation of the carbon of the charge at very high gasification rates and the fact that emulsion will be burned in the blast air stream, the temperature of the primary and secondary reduction zones will be maintained at ele vated temperatures, due to the sensible heat contained in the highly preheated products of combustion. A large percentage of sensible heat will be recovered owing to the reduction reactions and a large amount of the balance of the sensible heat will be extracted due to the thick bed of green coal above the reduction zone. There will be little loss due to the secondary oxidation in the upper gas zone, known as Neuman reversion, as a result of oxidation of CO by undeccmposed water vapor. Large amounts of water vapor can be used per pound of coal because of the higher oxi- 'diZ-ing zone temperatures which will tend to decompose more efiiciently the water vapor present.
Fuel gas is normally formed by the passage of a stream of steam and air through the thick bed of coal; primarily the reactions take place in three steps. The air and steam entering the incandescent bed of carbon above the ash line, causes i a rapid increase in the temperature. Due to this reaction, 02 plus 3.76 N2 equals CO2 plus 3.76 N2, the steam being preheated to the temperature of the oxidizing zone. This CO2, nitrogen. and superheated steam then passes into the primary rehigh.
equals CD plus Hz. None of the reduction reactions, of course, will take place until all of the oxygen present has'been consumed. These reactions also occur but ata reduced rate in the secondaryrcduction'zone and above this zone, the
hot gases will come in'contact with'theigreen coal that is being continuously 'fedinto the "producer, and as a result,the sensible heat contained in these gases distills off the volatile constituents from the coal. Inasmuch as'these volatiles are being distilled in the absence of air, they .contain materials for enriching the resulting gases.
in the event where this gas is being used hot "or as so-called smoked gas, these products of 'distillation are carried over with the gas and burned. But where these gases must be cleaned and cooled, such as in the operation of gas engines or heating coke ovens, the extracted tar becomes a problem. Also unlessrecuperative apparatus is installed, the sensible heat from the gas'at the final producer temperature is lost. The operations of these coal gas producers are limited at the present time by the following'factors.
The rate at which the coal maybe gaslfied ranges from 8.9 to about 100 pounds of coal per square foot of grate per hour. This is'determined by the fusion temperature of the ash in the coal as the producers are only equipped to dispose of unfused ash. Fusing of ash causes extreme difficulty from clinker formation. Fuel bed depth varies from 3.75 to 7 feet and pounds of steam per pound of coal varies from .28 to 1.57. Theoretically it would be best to use the amount of steam that would give the maximum efficiency of decomposition and therefore a minimum of dilution of the resulting gas with undecomposed steam. Under present operating conditions this cannot 'be done practically.
An excess of steam is generally-used in order to reduce the possibility of fusion of the ash and to obtain. a larger percentage of decomposed This usually defeats its own purpose because the reduction of steam being an endothermic reaction, the more steam used the lower the temperature of the reduction zone and therefore he lower percentage of the total steam decomno is also the disadvantage of having leoomposed steam in the final gas,'as secondczizidation of CO to CO2 occurs as a result of er vapor being present when the temperature By our method of operation we eliminate most of the above operating diificultiesand make it possible to convert all of the by-product tar into gas.
In the where washed or through tuyeres at high pressure'there is formed a combusition zone between the top of the slag and the under part of the coal charge. The emulsion being introduced at high velocity through a series of burners radially disposed around the wall of the producer, results in an off at right angles tends to maintain the slag in molten condition and to cause fusion of any ash being released from the combustion zone of the coke. The combustion of the emulsion also tends to preheat all the incoming air, as sufficient excess air must be supplied to get the necessary amount of heat release fromthe combustion of the carbon of the charge to form the CO2 necessary to react in the upper zone.
The incoming steam and water in the emulsion by passing through the body of this flame,is highly preheatedand then is further preheated by passing through the oxidation zone of incandescent carbon. These combined products of combustion highly preheated are then carried into primary reduction zone where due to the high temperature and the absence of oxygen reduction of the CO2 and water vapor occur. It is generally supposed that approximately of the uncombined hydrogen also reacts with the carbon to form CH4. These hot gases then pass through the secondary reduction zone where some further reduction occurs and are then passed through a thick bed of coal so as to cause distillation of the volatiles (if present) and a reduction in the sensible heat of the gases. The lower the final gas temperature can be carried, still maintaining high enough temperature to completely carry off the products of distillation, the more eflicient the operation will be, as there will be a saving in the sensible heat of the gas plus the fact that the lower the temperature, the less secondary oxidation there will be from the oxidizing effect of the undecomposed steam.-
It can easily be seen that complete gasification of coal can be efficiently carried out by this method of operation because of the fact that the fusion point of the ash in the coal will not be a limiting factor. Insofar as the rate of gasification is concerned this is made possible by the simultaneous burning of emulsified tars or fuel oils imparting enough heat, at what would nor- -mally be the ash zone, to maintain the ash in a liquid state. There is also the interesting fact that ash contains large amounts of iron oxide and silica with traces of titanium oxide, aluminum oxide, calcium oxide and magnesium. It is well known that iron, titanium, calcium and magnesium at highly elevated temperatures react catalytically to promote water gas and hydrogenation reactions. Inasmuch as all the liquid hydrocarbons, used for enriching, are passed through this zone of extreme high temperature and are in some cases, due to the high velocity of the incoming air, carried through the bed of incandescent coke, while still partly burned, complete thermal destruction takes place resulting in complete conversion to fixed gases of all of the liquid hydrocarbons charged. The slag can be periodically tapped out and disposed of In the foregoing description, we have set forth in considerable detail the manner in which our improved method will preferably be carried out in connection with the type of apparatus illustrated in the drawings, but the same is by way of illustration only, and all changes and variations are contemplated that come within the scope of the appended claims.
What we claim and desire to secure by Letters Patent is:
-l. In the production of combustible gas, introducinga mass of green substantially solid carbonaceous material into the upper portion of a stack and feeding the mass successively through a distillation zone, a reduction zone, an oxidation zone, and an incandescent zone, in the order named, maintaining the incandescent zone in a state of incandescence by blowing air into the lower portion of the mass, injecting an intimate mixture of water and fuel oil in atomized condition into the incandescent zone, burning the fuel oil and some of the resulting combustible gases in said incandescent zone, passing hot gases upwardly from the incandescent zone through said mass and thereby subjecting carbonaceous material above the zone of incandescence to distillation and partial combustion, and discharging the resulting gases from the upper portion of said distillation zone.
2. In the production of combustible gas, introducing a mass of green substantially solid carbonaceous material into the upper portion of a stack and feeding the mass successively downward through a distillation zone, a reduction zone, an oxidation zone, and an incandescent zone, in the order named, maintaining the incandescent zone in a state of incandescence by blowing air into the lower portion of the mass, injecting an intimate mixture of steam, water and fuel oil in atomized condition into the incandescent zone, burning the fuel oil and some of the resultant gases in said incandescent zone, passing other gases upwardly from the incandescent zone through said mass and thereby subjecting carbonaceous material above the zone of incandescence to distillation and to partial combustion, and discharging the resultant gas from the upper portion of said distillation zone.
3. In the production of combustible gas, introducing a mass of green substantially solid carbonaceous material into the upper portion of a stack and feeding the mass downwardly successively through a distillation zone, a reduction zone, an oxidation zone, and an incandescent zone, in the order named, maintaining the incandescent zone in a state of incandescence by blowing air into the lower portion of the mass, injecting an intimate mixture of water and fuel oil in atomized condition into the incandescent zone, burning the fuel oil and some of the resulting combustible gases in said incandescent zone, passing hot gases upwardly from the incandescent zone through said mass and thereby subjecting carbonaceous material above the zone of incandescence to distillation and partial combustion, and discharging the resulting gases from the distillation zone, the air introduced being sufficient to constantly maintain the lower portion of said zone incandescent and the ash in liquid condition.
4. In the production of combustible gas, introducing green carbonaceous material into a passageway at one point, feeding said material in the passageway successively through a distillation zone, a reduction zone, an oxidation zone, and an incandescent zone, in the order named, discharging slag in liquid condition from the passageway at another point remote from the first one and adjacent to the incandescent zone, raising a portion of the mass of carbonaceous material in the incandescent zone to a state of incandescence by blowing air into the incandescent zone, injecting an intimate mixture comprising water and fuel oil in atomized condition into the zone of incandescence, burning the fuel oil and some of the resulting combustible gases in the said incandescent zone, passing hot gases from the incandescent zone through the mass in a direction toward thepoint where the green carbonaceous material is introduced and thereby subjecting another portion of said carbonaceous material to distillation and partial combustion, and discharging the resulting gases from the mass at a point adjacent to that where the green carbonaceous material is introduced into the passageway.
5. In the production of combustible gas, introducing substantially solid carbonaceous material into the upper portion of a stack and feeding the material successively through a distillation zone, a reduction zone, an oxidation zone, and an in-, candescent zone, in the order named, before discharging slag in liquid condition from the lower portion of the stack, raising a portion of the mass of carbonaceous material adjacent the point of discharge of the slag, to a state of incandescence by blowing air into the incandescent zone, injecting a water-in-iuel oil emulsion in atomized condition into the zone of incandescence under superatmospheric pressure, burning some of the emulsion in said incandescent zone, passing hot gases from the incandescent zone through the mass in a direction toward the point where the green carbonaceous material is introduced and thereby subjecting another portion of said carbonaceous material to distillation and partial combustion, and discharging the resulting gases from the mass ,at a point adjacent to that where the green carbonaceous material is introduced into the mass.
6. In the production of combustible gas introducing a mass of green carbonaceous material into the upper portion of a stack and feeding the mass successively through a distillation zone, a reduction zone, an oxidation zone, and an incandescent zone, in the order named, maintaining the incandescent zone in incandescent condition by blowing air into the incandescent zone, injecting a liquid fuel comprising an intimate mixture of Water and fuel oil in atomized condition into the incandescent zone, burning the fuel oil and some of the resulting combustible gases in the incandescent zone, passing hot gases upwardly from the incandescent zone, through the oxidation zone, reduction zone and distillation zone and thereby subjecting carbonaceous material above the indancescent zone to distillation and partial combustion, and discharging the resulting gases from the distillation zone.
7. In the production of combustible, gas introducing a mass of green carbonaceous material into the upper portion of a stack and feeding the mass successively through a distillation zone, a reduction zone, an oxidation zone, and an incandescent zone, in the order named, maintaining the incandescent zone in incandescent condition by blowing air into the incandescent zone, injecting a liquid fuel comprising an intimate mixture of water and fuel oil in atomized condition into the incandescent zone, burning the fuel oil and some of the resulting combustible gases in the incandescent zone, passing hot gases upwardly from the incandescent zone, through the oxidation zone, reduction zone and distillation zone and thereby subjecting carbonaceous material above the incandescent zone to distillation and partial combustion, and discharging the resulting gases from the distillation zone, the air introduced into the incandescent zone being sufficient in quantity to maintain ash discharged from the incandescent zone, in liquid condition.
8. As an improvement in the art of manufacturing combustible gas, passing air upwardly through an incandescent mass of substantially solid carbonaceous material and a super-incumnaceousrma'terial arranged in superposed oxidation", reduction and distillation zones, injecting a: water-in-fueloil' emulsion in atomized condition into the incandescent body and burning the emulsion therein, passing hot gases from the incandescent body upwardly through said super in'a cumbent charge and thereby subjecting oarbonaceous material of the charge to distillation and partial combustion, and discharging the resulting gases from the distillation zone.
bent charge of fresh substantially solid carbonaceous material arranged in superposed oxidation, reduction and distillation zone, injecting a waterin-fuel oil emulsion in atomized condition into the incandescent body and burning the emulsion therein, passing hot gases from the incandescent body upwardly through said super-incumbent charge and thereby subjecting carbonaceous material of the charge to distillation and partial combustion, and discharging the resulting gases from the distillation zone, the amount of air introduced into the incandescent body being suflicient to cause the ash discharged to flow therefrom in liquid condition.
10. As an improvement in the art of manufacturing combustible gas, passing air upwardly through an incandescent mass of substantially solid carbonaceous material and a super-incumbent charge of fresh substantially solid carbonaceous material arranged in superposed oxidation reduction and distillation zones, injecting a water-in-fuel oil emulsion in atomized condition into the incandescent body and burning the emulsion therein, passing hot gases from the incandescent body upwardly through said super-incumbent charge and thereby subjecting carbonaceous material of the charge to distillation and partial combustion, and discharging the resulting gases from the distillation zone, the emulsion containing from approximately 25% to water.
11. In the production of combustible gas maintaining a column of substantially carbonaceous material in a stack having superposed distillation, reduction, oxidation and incandescent zones, raising the lower portion of the column to a state of incandescence by blowing air into the lower portion of the column, injecting a waterin-residual tar emulsion in atomized condition into the incandescent zone of the column, the water in the emulsion ranging from approximately 25% to 65%, burning at least some of the emulsion in said zone, passing hot gases upwardly from the incandescent zone successively through said oxidation, reduction and distillation zones and thereby subjecting th carbonaceous material above said incandescent zone to distillation and partial combustion, and discharging the resulting gases from the distillation zone.
12. In the production of combustible gas, introducing fresh coal into the upper portion of a stack and feeding the same downwardly in the stack successively through distillation, reduction, oxidation and incandescent zones, maintaining the incandescent zone in incandescent condition by simultaneously blowing air into the incandescent zone and injecting an intimate mixture of steam and a water-in-fuel oil emulsion in atomized condition, burning the fuel oil and some of the resulting combustible gases in the incanbent charge of fresh substantially solid carbodescent zone, passing hot gases upwardly from the incandescent zone successively through the oxidation, reduction and distillation zones, and thereby subjecting carbonaceous material above the incandescent zone to distillation and partial combustion, discharging resulting gases from the distillation zone, and discharging slag in fiowable condition from the lower portion of the incandescent zone.
13. In a production of combustible gas, maintaining a substantially vertical column of substantially solid carbonaceous material in a stack, heating the bottom portion of the column to a state of incandescence by blowing air into the lower portion of the column, making a water-infuel oil emulsion of predetermined quantities of water and fuel oil and injecting such emulsion in atomized condition into the lower portion of the incandescent zone of the column in intimate admixture with steam, burning the fuel oil and some of the resulting combustible gases in said zone, passing hot gases solely from said zone upwardly through said column and. thereby subjecting carbonaceous material of the column above said zone to distillation and partial combustion, and discharging the resulting gases from the upper portion of said column.
MARVIN W. DITTO. WILLIAM P. TORRINGTON.
US309504A 1939-12-15 1939-12-15 Fuel gas production Expired - Lifetime US2281562A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US309504A US2281562A (en) 1939-12-15 1939-12-15 Fuel gas production

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US309504A US2281562A (en) 1939-12-15 1939-12-15 Fuel gas production

Publications (1)

Publication Number Publication Date
US2281562A true US2281562A (en) 1942-05-05

Family

ID=23198504

Family Applications (1)

Application Number Title Priority Date Filing Date
US309504A Expired - Lifetime US2281562A (en) 1939-12-15 1939-12-15 Fuel gas production

Country Status (1)

Country Link
US (1) US2281562A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3118746A (en) * 1956-07-13 1964-01-21 Texaco Development Corp Generation of fuel gas from oil shale
USB375220I5 (en) * 1973-06-29 1975-01-28
US4257782A (en) * 1979-08-27 1981-03-24 General Electric Company Coal gasification process
WO2005047435A3 (en) * 2003-11-04 2006-10-12 Iti Ltd Catalytic gasification
CN102797557A (en) * 2012-09-05 2012-11-28 昆明理工大学 Internal-combustion engine capable of directly burning firewood
WO2013057133A1 (en) * 2011-10-21 2013-04-25 Shell Internationale Research Maatschappij B.V. Gasification reactor
US8721748B1 (en) * 2013-01-28 2014-05-13 PHG Energy, LLC Device with dilated oxidation zone for gasifying feedstock
US11242494B2 (en) 2013-01-28 2022-02-08 Aries Clean Technologies Llc System and process for continuous production of contaminate free, size specific biochar following gasification

Cited By (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3118746A (en) * 1956-07-13 1964-01-21 Texaco Development Corp Generation of fuel gas from oil shale
USB375220I5 (en) * 1973-06-29 1975-01-28
US3920417A (en) * 1973-06-29 1975-11-18 Combustion Eng Method of gasifying carbonaceous material
US4257782A (en) * 1979-08-27 1981-03-24 General Electric Company Coal gasification process
US8486168B2 (en) 2003-11-04 2013-07-16 Iti Energy Limited Gasification
WO2005047435A3 (en) * 2003-11-04 2006-10-12 Iti Ltd Catalytic gasification
US20060265954A1 (en) * 2003-11-04 2006-11-30 Iti Limited Gasification
EA009349B1 (en) * 2003-11-04 2007-12-28 Ай Ти Ай ЛИМИТЕД Gasifier and method of solid fuel gasification
US8252072B2 (en) 2003-11-04 2012-08-28 Iti Energy Limited Gasification
CN103857773A (en) * 2011-10-21 2014-06-11 国际壳牌研究有限公司 Gasification reactor
WO2013057133A1 (en) * 2011-10-21 2013-04-25 Shell Internationale Research Maatschappij B.V. Gasification reactor
AU2012324965B2 (en) * 2011-10-21 2015-06-11 Air Products And Chemicals, Inc. Gasification reactor
US9382488B2 (en) 2011-10-21 2016-07-05 Shell Oil Company Gasification reactor
CN103857773B (en) * 2011-10-21 2017-02-15 国际壳牌研究有限公司 Gasification reactor
CN102797557A (en) * 2012-09-05 2012-11-28 昆明理工大学 Internal-combustion engine capable of directly burning firewood
US8721748B1 (en) * 2013-01-28 2014-05-13 PHG Energy, LLC Device with dilated oxidation zone for gasifying feedstock
US9375694B2 (en) 2013-01-28 2016-06-28 PHG Energy, LLC Device with dilated oxidation zone for gasifying feedstock
US11242494B2 (en) 2013-01-28 2022-02-08 Aries Clean Technologies Llc System and process for continuous production of contaminate free, size specific biochar following gasification
US11566191B2 (en) 2013-01-28 2023-01-31 Aries Clean Technologies Llc System and process for continuous production of contaminate free, size specific biochar following gasification

Similar Documents

Publication Publication Date Title
US4153426A (en) Synthetic gas production
US4504043A (en) Apparatus for coal-gasification and making pig iron
US2805188A (en) Process for producing synthesis gas and coke
PL135926B1 (en) Method of and apparatus for gasifying carbon containing materials
US3998606A (en) Method and apparatus for manufacturing reducing gas
US2302156A (en) Process and apparatus for the production of useful fuel gas
CN101448962B (en) Method for manufacturing molten irons by injecting a hydrocarbon gas and apparatus for manufacturing molten irons using the same
GB2169310A (en) Gas production
US2281562A (en) Fuel gas production
US2976134A (en) Hydrocarbon conversion process
US1799885A (en) Process of generating producer gas
US1738620A (en) Catalytic gas generator
US1098534A (en) Method of and apparatus for generating producer-gas.
US2898204A (en) Process for production of combustible gases
US4002534A (en) Continuous coking process
US1938139A (en) Method of producing combustible gas
US2905544A (en) Suspension process for the production of co and h2 from a solid carbonaceous fuel, oxygen and steam
US3088816A (en) Method and apparatus for the dry ash generation of hydrogen and carbon monoxide gases from solid fuels
JPS6154354B2 (en)
US2770536A (en) Method for gasification of solid fuels
US2751287A (en) Gasification of fuels
US1964207A (en) Process of manufacturing producer gas of high calorific value
US2663625A (en) Oil gas process and apparatus
US2204001A (en) Production of water gas
US2054154A (en) Method of manufacturing combustible gas