US2217250A - Production of oil gas - Google Patents
Production of oil gas Download PDFInfo
- Publication number
- US2217250A US2217250A US238929A US23892938A US2217250A US 2217250 A US2217250 A US 2217250A US 238929 A US238929 A US 238929A US 23892938 A US23892938 A US 23892938A US 2217250 A US2217250 A US 2217250A
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- Prior art keywords
- gas
- oil
- density
- products
- temperature
- 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
Links
- 238000004519 manufacturing process Methods 0.000 title description 15
- 239000007789 gas Substances 0.000 description 79
- 239000003921 oil Substances 0.000 description 37
- 239000006227 byproduct Substances 0.000 description 20
- 238000000034 method Methods 0.000 description 11
- 239000003502 gasoline Substances 0.000 description 10
- 229930195733 hydrocarbon Natural products 0.000 description 10
- 150000002430 hydrocarbons Chemical class 0.000 description 10
- 239000000047 product Substances 0.000 description 8
- 239000007788 liquid Substances 0.000 description 7
- 239000000203 mixture Substances 0.000 description 6
- 238000009835 boiling Methods 0.000 description 5
- 230000003467 diminishing effect Effects 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 239000003208 petroleum Substances 0.000 description 5
- 230000001105 regulatory effect Effects 0.000 description 5
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 4
- 230000005484 gravity Effects 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- 238000010304 firing Methods 0.000 description 3
- 238000002309 gasification Methods 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 230000002596 correlated effect Effects 0.000 description 2
- 230000000875 corresponding effect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- -1 ethylene, propylene Chemical group 0.000 description 2
- 239000000295 fuel oil Substances 0.000 description 2
- 239000006233 lamp black Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 125000004805 propylene group Chemical class [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 238000012935 Averaging Methods 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 239000008161 low-grade oil Substances 0.000 description 1
- 238000013021 overheating Methods 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000002407 reforming Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000000153 supplemental effect Effects 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G9/00—Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
Definitions
- This invention relat s to the production of oil gas; and it comprises an improvement in methods of making oil gas in intermittently heated hot checkerwork chambers, the improvement consisting in feeding petroleum oil into the chamber at a diminishing rate generally corresponding with the drop in temperature during the run, the rate of oil introduction being so controlled as to maintain an efiluent gas of constant character, constancy being usually ascertained by observation of the density of the eiiluent gas; the gas being then freed of non-gaseous components and re-treated in a checker under like condition, that is, with a diminishing feed as the temperature of the checker drops; all as more fully hereinafter set forth and as claimed.
- the difliculty is 55 met by making a high temperature lean gas and a low temperature rich gas as separate operations and mixing the two.
- the checkerwork or other form of refractory contact surface is best preheated to a temperature above that at which a gas and by-products of the desired composition are produced by the ordinary method. If, for example, products of the 1 character ordinarily obtained in the intermedi- ;85
- the initial temperature of the refractory contact surface should be substantially higher than 1600" F.
- the upper limit of temperatures for the production of gas and by-products of any desired composition is not critical except as limited by practical operating considerations and apparatus size. With higher temperatures longer production cycles are obtainable and the character of the products obtained can be regulated by regulating the rate of oil feed. For example, when products of the character produced in the intermediate temperature range are desired, a convenient initial op.- erating temperature is about 1650 F. However, higher initial temperatures such as 1800 to 2000" F. may be used and the same type of products produced by using an increased rate of oil feed. V
- a checkerwork of refractory brick was heated to a temperature of about 1650 F. by internal firing. Oil was then sprayed into the chamber at a rate sufiicient to produce an eiiluent gas having a density about 0.74 of that of air at the ordinary temperature and pressure. The rate of oil feed was progressively decreased to maintain the density of the efliuent substantially constant. At the end of the run the rate of oil feed had been reduced to about one-third that at the beginning and the temperature of the refractory checkerwork had dropped about 320 F. to a final temperature of about 1330 F.
- the method of my invention may be utilized repeatedly in a sin gle manufacturing process, in conjunction with various supplemental operations in order to effect best results.
- the manufacturing process may involve the following steps:
- Petroleum oil is introduced into a preheated refractory checkerwork with a properly adjusted density of the eiiiuent and a properly tapered oil input to produce in each run a substantially uniform quality of effluent gas of high heat value (1000 to 1500 B. t. u. per cubic foot as desired) which contains from 5 to 20 per cent of olefines including propylenes and butylenes together with substantial quantities of gasoline and benzol, the residuum being a tar containing more or less of the original oil.
- the efliuent is passed through suitable condensing apparatus for removal of tar, gasoline and benzol.
- the gas, now substantially free of readily condensable hydrocarbons may then be treated by any suitable polymerization process such as catalytic or thermal processes to convert the propylene and butylenes into polymer gasoline.
- the residual gas which is still rather rich (900-1400 B. t. u. per cubic foot) is then passed on to the next step.
- the gas maybe re-formed by being introduced into a second refractory checker-work heated to a temperature higher than that used in the first step, the purpose being to increase the volume of the gas and reduce the heat value to about 570 B. t. u. per cubic foot.
- the rate of introduction of the hydrocarbons is correlated'with the density of the effluent gas to obtain products of the desired quality throughout the run.
- the by-products formed during this step may include small amounts of benzol, lampblack and tar.
- the by-products and gas are condensed and recovered in known ways. .
- the eiiluent gas is suitable for domestic and industrial supplies.
- the residual tar recovered in the first step may be sold as such or processed to produce road oils or the like or it may be used as the raw material for the production of further amounts of gas.
- the tar may be heated at a rather high temperature to produce a gas having a heat content of say 450 to 500 B. t. u. per cubic foot and this lean gas may be blended with richer gas to produce a city gas. so that the output of the entire gas works will have a heat value of about '70 B. t. u. per cubic foot.
- the input of tar and the density of the eiliuent gases may again be correlated according to the method of my invention to produce a gas of uniform quality throughout the run.
- I cite an operation in which the oil gasified was a typical cracked oil residue of 12 A. P. I. This was run through a hot checker in the way described with the eiliuent density maintained at 0.83. A large yield of liquid hydrocarbon boiling in the gasoline range was obtained. The condensed oils were 70 per cent aromatic. The amount was 3.5 gallons per 1000 cubic feet of 0.83 gas. The gas from this operation was then further cracked in a second generator to produce a resultant gas of 5'70 B. t.
- the improvement which comprises introducing the oil into preheated checkerwork at an initial rate which is regulated to yield a gaseous effluent having a substantial by-product content and having a definite density after removal of condensable by-products therefrom, gradually reducing the oil flow as the checkerwork cools, this reduction in the oil flow being at a rate so con-.
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Description
Patented Oct. 8, 1940 UNITED STATES PATENT OFFICE PRODUCTION OF OIL GAS No Drawing. Application November 4, 1938, Serial No. 238,929
4 Claims.
This invention relat s to the production of oil gas; and it comprises an improvement in methods of making oil gas in intermittently heated hot checkerwork chambers, the improvement consisting in feeding petroleum oil into the chamber at a diminishing rate generally corresponding with the drop in temperature during the run, the rate of oil introduction being so controlled as to maintain an efiluent gas of constant character, constancy being usually ascertained by observation of the density of the eiiluent gas; the gas being then freed of non-gaseous components and re-treated in a checker under like condition, that is, with a diminishing feed as the temperature of the checker drops; all as more fully hereinafter set forth and as claimed.
In the commercial production of gas for heating and lighting from low grade petroleum oils, such as gas oil, fuel oil, etc., it is customary to perform the gasification in intermittently heated hot checker chambers. Heating is effected by burning oil or gas in the checker until it reaches a high temperature, say 1600 to 2000 F. Oil is then fed into the heated checker chamber as long as there is enough heat to effect a substantial amount of gasification. The character of gas produced during the run is not constant, but varies. Storage and averaging are required.
Not all the oil can be converted into gas, there being an incidental production of by-products. These by-products help defray the cost of operation and it is an object to recover them in salable form. In certain prior Patents Nos. 1,409,709 and 1,466,648, whereon the present invention is in some aspects an improvement, I have discussed the formation and recovery of by-products in making oil gas.
In a general way it may be said that oil heated to any very high temperature tends to give a great volume of gas of low heating value, while at low gasification temperatures the converse is true. At very high temperatures there is a tendency toward the production of hydrogen, aroo matic oils, tar and pitch, while at low temperatures the side products are more of the nature of gasoline and kerosene and fuel oil. In making oil gas in a hot checker work, both types of action occur; the gas and by-products are of both types.
All these things are well recognized in the art. It is also recognized that it is diflicult to obtain a standard city gas of, say, 500 to 600 B. t. u. in
4 a single operation. Sometimes the difliculty is 55 met by making a high temperature lean gas and a low temperature rich gas as separate operations and mixing the two.
I have discovered that in gasifying oil in a checker a much more constant product can be obtained throughout a run by feeding oil at a 5 diminishing rate corresponding roughly to the drop in temperature in the checker and correlating the feed with the character of the gas produced. The effort is to so correlate the feed as -to obtain an eiliuent gas of constant density. 10
Operating in this way it is easy to make a gas of constant composition during a run and to obtain the same character of gas in different runs. The operation may be so conducted, for example, as to give a gas of, say, 0.74 per cent apparent 15 density as compared withatmospheric air at 60 F. As the gas leaves the checker it carries condensable matter with it and comparative observation of density must be made after cooling to the ordinary temperature.
Gas made in the checker in the described way is unduly high in fuel value and it is often worth while to polymerize the ethylene, propylene and butylenes in part and remove a condensate of light oils. Or the olefins may be utilized for 25 chemical purposes; in the manufacture of chlorhydrins, chlorides, glycols, etc. 7
It is of course feasible to dilute down the rich gas with lean gas, with or without polymerizing treatments.
But I find the best results are obtained by making a rich gas as described, removing condensable oils, with or without some polymerization to add to their amount, and then re-forming and standardizing the gas by passage through an- 35 other checker fired at intervals. As before, the feed through the checker in a run is gradually lessened as the heat drops and is controlled by the observed density of the issuing gas, the density being kept constant. Volatiles accompanying the re-formed gas are condensed and collected.
With a double operation of this type a high yield of commercial gas of standard type can be secured, with an abundant production of high grade by-products, in tolerably direct operation; that .is, without the necessity of storage and blending of great volumes of gas.
A good yield of condensable oil'is obtained at each stage and there is a good utilization-of the 5 low grade oil treated in the yield of gas and of by-products taken together.
By utilization of what may be termed a "tapered feed, overheating and underheating are obviated and a constant efliuent of accurately predetermined character is obtained in each operation- While the invention is based upon the fact that the continually changing temperature conditions within an intermitttently heated chamber should be compensated by regulation of the input 'of petroleum hydrocarbons, it is found that a simple pyrometric determination of the temperature at any point within the chamber is not an adequate means of control. The conditions within a preheated checkerwork are complex and the surface temperature of the brickwork at any instant is onlyroughly related to the rate and character of the decomposition of the oil which takes place. Other factors such as the ratio of refractory surface to the volume of the passing hydrocarbon, the conductivity of the refractory, the total amount of heat stored in the refractory and the like, affect the heat transfer to the gas and thus affect the composition of the resultant products. On the other hand, by correlating the input of the hydrocarbon with a property of the efiluent gas such as the density, all the complicated factors are compensated for at once and an eflluent of substantially constant composition may be readily obtained. This is done in the present invention.
In carrying out the method of my invention, the checkerwork or other form of refractory contact surface is best preheated to a temperature above that at which a gas and by-products of the desired composition are produced by the ordinary method. If, for example, products of the 1 character ordinarily obtained in the intermedi- ;85
ate temperature range of 1200 to 1600 F., as described above, are desired, the initial temperature of the refractory contact surface should be substantially higher than 1600" F. The upper limit of temperatures for the production of gas and by-products of any desired composition is not critical except as limited by practical operating considerations and apparatus size. With higher temperatures longer production cycles are obtainable and the character of the products obtained can be regulated by regulating the rate of oil feed. For example, when products of the character produced in the intermediate temperature range are desired, a convenient initial op.- erating temperature is about 1650 F. However, higher initial temperatures such as 1800 to 2000" F. may be used and the same type of products produced by using an increased rate of oil feed. V
In practical operation, after the checker has been heated by internal firing, oil is fed in and the feed continued through the run at a diminishing rate as described. After firing the checker is left full of hot products of combustion and these mix with and dilute the first portions of gas made. .This must be allowed for in taking the density in the first stage.
The character of the gas made and of the byproducts obtained by controlling the density of the eflluent at difierent values varies. ample, the specific gravity is controlled at values on the order of 0.4 (air=1 at 60 F., atmos: pheric pressure), large volumes of gas of relativelylow heating value are produced with but little yield of condensable by-products, say about one-half gallon of 400 F. end-point liquids per 1000 cubic feet of gas. n the other hand at a relatively high specific gravity such as 0.83 a yield as high as four gallons of 400 E. P. liquid per 1000 cubic feet of gas may be obtained together with a smaller volume of gas of higher If, for exheating value. Good yields of gas of high heating value and of valuable by-products are obtainable, for example, when the specific gravity .is controlled at 0.74 to 0.75 or 0.78 to 0.79. In
accordance with common usage in this art, the terms density and specific gravity are used interchangeably herein; and in both cases, numerical values are based on air (at standard conditions) =1.
In a typical operation according to the method of my present invention, a checkerwork of refractory brick was heated to a temperature of about 1650 F. by internal firing. Oil was then sprayed into the chamber at a rate sufiicient to produce an eiiluent gas having a density about 0.74 of that of air at the ordinary temperature and pressure. The rate of oil feed was progressively decreased to maintain the density of the efliuent substantially constant. At the end of the run the rate of oil feed had been reduced to about one-third that at the beginning and the temperature of the refractory checkerwork had dropped about 320 F. to a final temperature of about 1330 F.
In commercial operation the method of my invention may be utilized repeatedly in a sin gle manufacturing process, in conjunction with various supplemental operations in order to effect best results. For example, in a typical complete gas making system producing a city gas of 570 B. t. u. per cubic foot together with byproducts as gasoline, benzol, higher olefines, tar and lampblack, the manufacturing process may involve the following steps:
(I) Petroleum oil is introduced into a preheated refractory checkerwork with a properly adjusted density of the eiiiuent and a properly tapered oil input to produce in each run a substantially uniform quality of effluent gas of high heat value (1000 to 1500 B. t. u. per cubic foot as desired) which contains from 5 to 20 per cent of olefines including propylenes and butylenes together with substantial quantities of gasoline and benzol, the residuum being a tar containing more or less of the original oil. The efliuent is passed through suitable condensing apparatus for removal of tar, gasoline and benzol. The gas, now substantially free of readily condensable hydrocarbons may then be treated by any suitable polymerization process such as catalytic or thermal processes to convert the propylene and butylenes into polymer gasoline. The residual gas which is still rather rich (900-1400 B. t. u. per cubic foot) is then passed on to the next step.
(H) In this step the gas maybe re-formed by being introduced into a second refractory checker-work heated to a temperature higher than that used in the first step, the purpose being to increase the volume of the gas and reduce the heat value to about 570 B. t. u. per cubic foot. During this step the method of my invention is again applied. The rate of introduction of the hydrocarbons is correlated'with the density of the effluent gas to obtain products of the desired quality throughout the run. The by-products formed during this step may include small amounts of benzol, lampblack and tar. The by-products and gas are condensed and recovered in known ways. .The eiiluent gas is suitable for domestic and industrial supplies.
(III) The residual tar recovered in the first step may be sold as such or processed to produce road oils or the like or it may be used as the raw material for the production of further amounts of gas. In this case the tar may be heated at a rather high temperature to produce a gas having a heat content of say 450 to 500 B. t. u. per cubic foot and this lean gas may be blended with richer gas to produce a city gas. so that the output of the entire gas works will have a heat value of about '70 B. t. u. per cubic foot. In the production of this lean gas the input of tar and the density of the eiliuent gases may again be correlated according to the method of my invention to produce a gas of uniform quality throughout the run.
As illustrative, I cite an operation in which the oil gasified was a typical cracked oil residue of 12 A. P. I. This was run through a hot checker in the way described with the eiliuent density maintained at 0.83. A large yield of liquid hydrocarbon boiling in the gasoline range was obtained. The condensed oils were 70 per cent aromatic. The amount was 3.5 gallons per 1000 cubic feet of 0.83 gas. The gas from this operation was then further cracked in a second generator to produce a resultant gas of 5'70 B. t. u of density approximately 0.4, with an additional yield of liquid hydrocarbons boiling in the gasoline range of 0.75 gallon per thousand cubic feet of 0.83 gas, making a total recovery for both operations of 4.25 gallons of highly aromatic liquid hydrocarbons boiling in the gasoline range. This quantity amounts to 3.05 gallons per thousand cubic feet of 0.4 density final gas.
When the tar resulting from the first operation was gasified to produce additional quantities of domestic or 0.4 density gas, an additional quantity of liquid hydrocarbons boiling in the gasoline range amounting to 0.5 gallon per thousand cubic feet of 0.4 density gas was produced, making a total yield of liquid hydrocarbons boiling in the gasoline range of 2.28 gallons per thousand cubic feet of 0.4 density gas from the reforming and tar cracking operations.
What I claim is:
1. In the production of gas and by-products from petroleum oils by pyrolysis in intermittently heated checkerwork, with removal and collection of the gas formed and recovery of by-products, the improvement which comprises introducing the oil into preheated checkerwork at an initial rate which is regulated to yield a gaseous effluent having a substantial by-product content and having a definite density after removal of condensable by-products therefrom, gradually reducing the oil flow as the checkerwork cools, this reduction in the oil flow being at a rate so con-. trolled as to maintain the density of the gaseous eflluent substantially constant throughout the run after removal of condensable by-products therefrom, removing condensable constituents from the said gaseous efl'luent, introducing the resulting gas into a second preheated checkerwork at an initial rate regulated to yield a gaseous effluent of a different density, and diminishing the rate of gas introduction as the said second checkerwork cools to maintain the density of the gaseous efliuent therefrom substantially constant.
2. The method of claim 1, wherein the said oil flow is so regulated that the density of the gas produced therefrom is maintained between 0.74 and 0.79.
3. The method of claim 1, wherein the checkerwork into which the said oil is introduced is preheated to a temperature above 1600 F., and the run is stopped when the temperature falls to about 1330" F.
4. The method of claim 1, wherein the said condensable constituents removed from the gas
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US238929A US2217250A (en) | 1938-11-04 | 1938-11-04 | Production of oil gas |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US238929A US2217250A (en) | 1938-11-04 | 1938-11-04 | Production of oil gas |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2217250A true US2217250A (en) | 1940-10-08 |
Family
ID=22899910
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US238929A Expired - Lifetime US2217250A (en) | 1938-11-04 | 1938-11-04 | Production of oil gas |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2217250A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2442093A (en) * | 1945-06-18 | 1948-05-25 | United Gas Improvement Co | Pyrolysis of fluid hydrocarbons |
| US2470578A (en) * | 1942-10-03 | 1949-05-17 | Percy H Royster | Thermal molecular alteration of carbon compounds |
| US2707675A (en) * | 1952-02-11 | 1955-05-03 | Inst Gas Technology | Method of preparing fuel gas interchangeable with natural gas |
| US2714060A (en) * | 1951-03-07 | 1955-07-26 | Stark Virgil | Process of treating oilgas to produce utility gas of low heat content and low gravity with valuable by-products |
| US2721122A (en) * | 1952-09-24 | 1955-10-18 | Inst Gas Technology | Thermal method of making oil gas |
| US2730437A (en) * | 1951-04-07 | 1956-01-10 | Raymond B Coombe | Automatic control for gas making machines |
-
1938
- 1938-11-04 US US238929A patent/US2217250A/en not_active Expired - Lifetime
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2470578A (en) * | 1942-10-03 | 1949-05-17 | Percy H Royster | Thermal molecular alteration of carbon compounds |
| US2442093A (en) * | 1945-06-18 | 1948-05-25 | United Gas Improvement Co | Pyrolysis of fluid hydrocarbons |
| US2714060A (en) * | 1951-03-07 | 1955-07-26 | Stark Virgil | Process of treating oilgas to produce utility gas of low heat content and low gravity with valuable by-products |
| US2730437A (en) * | 1951-04-07 | 1956-01-10 | Raymond B Coombe | Automatic control for gas making machines |
| US2707675A (en) * | 1952-02-11 | 1955-05-03 | Inst Gas Technology | Method of preparing fuel gas interchangeable with natural gas |
| US2721122A (en) * | 1952-09-24 | 1955-10-18 | Inst Gas Technology | Thermal method of making oil gas |
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