US1850291A - Process of cracking oil - Google Patents
Process of cracking oil Download PDFInfo
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- US1850291A US1850291A US244095A US24409528A US1850291A US 1850291 A US1850291 A US 1850291A US 244095 A US244095 A US 244095A US 24409528 A US24409528 A US 24409528A US 1850291 A US1850291 A US 1850291A
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- chamber
- oil
- cracking
- vapors
- gases
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- 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
- C10G9/34—Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils by direct contact with inert preheated fluids, e.g. with molten metals or salts
- C10G9/36—Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils by direct contact with inert preheated fluids, e.g. with molten metals or salts with heated gases or vapours
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- 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
- C10G9/34—Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils by direct contact with inert preheated fluids, e.g. with molten metals or salts
- C10G9/36—Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils by direct contact with inert preheated fluids, e.g. with molten metals or salts with heated gases or vapours
- C10G9/38—Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils by direct contact with inert preheated fluids, e.g. with molten metals or salts with heated gases or vapours produced by partial combustion of the material to be cracked or by combustion of another hydrocarbon
Definitions
- This invention relates to improvements in process of cracking oil, and is more particularly directed to what is generally known as vapor phase crackin
- the crude petro eum or other hydrocarbon oil to be treated is first preferabl subjected to a relatively mild cracking an separated therein into a relatively large percentage of vapors on the one hand and into a liq- 19 uid residue on the other hand.
- Thisy initial cracking step is intended to produce a residue, which is relatively free from carbon .containing particles, but which also contains those heavier constituents, which if subjected to vapor phase cracking would tendto undue production of coke or carbon.
- the vapors more or less free from coke or carbon forming constituents arethen subjected to a more severe vapor phase cracking reaction.
- 1 designates a furnace provided with a burner, under pressure.
- a heating coll 3 provided with inlet pum 4 leading to any suitable source of oil su py.
- the temperature of the gases of combustion is regulated through the cooling coil 9 through which may be circulated any suitable cooling medium.
- the temperature of. the gases is preferablyy sufficiently reduced so that the oil in the chamber 6 is heated to an oil temperature of say 700 to 900 F., more or less; vaporization takes place in the chamber 6 and the vapors together with the gases of combustion pass through theconduit 10,.
- the rllhe vaporsin the chamber 12 are superheated, say to a temperature of 1000o F., or more by means of the furnace 13 and burner 14.
- This burner 14, as Well as burner 2 are equipped with suitable pumps, so that combustion can take place under the pressure of the system.
- the vapors in the chamber 12 are superheated, say to a temperature of 1000o F., or more by means of the furnace 13 and burner 14.
- This burner 14, as Well as burner 2 are equipped with suitable pumps, so that combustion can take place under the pressure of the system.
- the rllhe vaporsin the chamber 12 are superheated, say to a temperature of 1000o F., or more by means of the furnace 13 and burner 14.
- This burner 14, as Well as burner 2 are equipped with suitable pumps, so that combustion can take place under the pressure of the system.
- the temperature of the gases from the furnace 13 as they pass through the conduit 15 may be controlled by means of the cooling coil 16 through which a suitable coolingmedium may be circulated.
- the vapor phase cracking chamber 12 may be provided with a drainplpe 17, having throttle valve 18.
- the va pors in the chamber 12 are, as heretofore stated, subjected to this vapor phase cracking reaction at relatively elevated temperatures,
- the vapors and gases pass out of the lower portion of chamber 12 through the conduit 19 into the lower side of a dephlegmator 20.
- the temperature of this dephlegmator may be controlled by a suitable coil 21 through which may be circulated cold oil or otller'cooling medium. .
- the temperature of the dephlegmator .2 0 is so controlled that the sufficiently cracked vapors as, for example, gasoline like bodies, will not be condensed andpass through the condenser coil 22' into the receiver 23.
- This receiver 23 is provided with distillate draw-od' pipe 24 having throttle valve 25 and gas outlet pipe 26, having throttle valve 27.
- the insuiciently cracked vapors are condensed in the dephlegmator 20 and may be returned as reflux condensate to the chamber 6' by means of the pipe 28 and pump 29, or, if desired,
- valves 32, 33, 34 and 35 may be returned to the chamber 12 through the pipe 30 or, if desired, part of the reflux maybe drawn out of ⁇ the system through branch v31.
- I provide the valves 32, 33, 34 and 35, as shown.
- the uncondensible gases from the receiver 23, in Whole or in part, may be returned to the system by means of the gas line 37, having throttle valve 38, pump 39 and feed line 40; thence, from feed line 40, either to the chamber 6, through branch 41, having throttle valve 42 or to the chamber 13 throughbranch 43, having throttle valve 44.
- the arrangement is such that the uncondensible gases may be returned either to chamber 6 or chamber 13 or to both chambers.
- the oil to be treated may be crude, topped crude, fuel oil or distillates. The extent to which the cracking reaction Will take place Will vary With the kind of charging stock treated and the products desired.
- the cracking in the chamber 6 may be controlled entirely independently of the extent of the cracking that may take place in the vapor phase chamber 12 In certain cases, it may be desirable to introduce a'catalyst into the cracking chambers as, for example, iron oxide, nickel or MoneI metal.
- a process of cracking hydrocarbon oil consisting in subjecting the oil to an initial cracking step, separating the oils into vapors relatively free from coke forming constituents and into residue, isolating said residue from the process subjecting such vapors freed of said residue to a vapor phase cracking reaction as a second cracking step, in both the said steps subjecting the oil constituents to the direct physical contact action of temperature controlled combustion gases, passing the vapors from the second cracking step to a reiiux condenser, separating the suiiiciently and insuiciently cracked vapors in said refiux condenser and recracking the reflux condensate.
- a process for cracking hydrocarbon oil consisting in subjecting the oil to an initial cracking step, separating the oils into vapors relatively free from coke forming constituents and into residue, isolating said residue from thc process, subjecting such vapors freed of said residue to a vapor phase cracking reaction as a second cracking step, in both the said steps subjecting the oil constituents to the direct action of separately temperature controlled combustion gases, passing thc vapors from the second cracking step to a reflux condenser, separating the suticiently and insuiiciently cracked vapors in said reflux condenser and recrackmg the reiux condensate, and introducing incondensible gases which have passed out of the reflux condenser back into contact with the oil being cracked.
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- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Combustion & Propulsion (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Description
PROCESS 0F CRACKING OIL Filed Jan. 3. 1928 Patented Mar. 22, 1932 UNITED STATES PATENT OFFICE JEAN DELATTBE SIIGU'Y, OF CHICAGO, ILLINOIS, ASSIGNOR TO UNIVERSAL OIL PRODUCTS COMPANY, OF CHICAGO, ILLINOIS, A CORPORATION OF SOUTH DAKOTA PROCESS OF CRAC'KING OIL Application filed lilamxary 8, 1928. Serial No.' 244,095.
This invention relates to improvements in process of cracking oil, and is more particularly directed to what is generally known as vapor phase crackin In the present invention, the crude petro eum or other hydrocarbon oil to be treated is first preferabl subjected to a relatively mild cracking an separated therein into a relatively large percentage of vapors on the one hand and into a liq- 19 uid residue on the other hand. Thisy initial cracking step is intended to produce a residue, which is relatively free from carbon .containing particles, but which also contains those heavier constituents, which if subjected to vapor phase cracking would tendto undue production of coke or carbon. The vapors more or less free from coke or carbon forming constituents arethen subjected to a more severe vapor phase cracking reaction. an In order to understand the invention, I
have shown. the accompanying drawing in I which anV apparatus is diagrammatically shown suitable for carrying out the yinvenption., Thise`drawing is, as stated, diagrammatic and in no sense to scale.
Referring to the drawing, 1 designates a furnace provided with a burner, under pressure. In the upper portion of the furnace is located a heating coll 3, provided with inlet pum 4 leading to any suitable source of oil su py.
he gases of combustion ppss through the fl'ue 5 into the initial crac 'ng chamber 6. The preheated oil is introduced into the upper end of the chamber, as shown through the pipe 7, having throttle valve 8.
The temperature of the gases of combustion is regulated through the cooling coil 9 through which may be circulated any suitable cooling medium. The temperature of. the gases is preferablyy sufficiently reduced so that the oil in the chamber 6 is heated to an oil temperature of say 700 to 900 F., more or less; vaporization takes place in the chamber 6 and the vapors together with the gases of combustion pass through theconduit 10,.
having throttle or pressure reducing` valve 11 into the vapor phase cracking chamber 12. The liquid residue is continuousl drawn out of the chamberv 6 through the raw-off pipe 13, having throttle valve 14. It is preferable to maintain a relatively low liquid level in the chamber 6, for example, as shown at the dotted line a. A pressure of say may be maintained in the chamber 6 by slutably regulating the valves 11 .and 14, pump 4 and burner 2.
rllhe vaporsin the chamber 12 are superheated, say to a temperature of 1000o F., or more by means of the furnace 13 and burner 14. This burner 14, as Well as burner 2, are equipped with suitable pumps, so that combustion can take place under the pressure of the system. In order to prevent over-heating of the vapors in the chamber 12, the
temperature of the gases from the furnace 13 as they pass through the conduit 15 may be controlled by means of the cooling coil 16 through which a suitable coolingmedium may be circulated. The vapor phase cracking chamber 12 may be provided with a drainplpe 17, having throttle valve 18. The va pors in the chamber 12 are, as heretofore stated, subjected to this vapor phase cracking reaction at relatively elevated temperatures,
thereby producing substantial quantities of unsaturates, aromatics or anti-knock compounds. The vapors and gases pass out of the lower portion of chamber 12 through the conduit 19 into the lower side of a dephlegmator 20. The temperature of this dephlegmator may be controlled by a suitable coil 21 through which may be circulated cold oil or otller'cooling medium. .The temperature of the dephlegmator .2 0 is so controlled that the sufficiently cracked vapors as, for example, gasoline like bodies, will not be condensed andpass through the condenser coil 22' into the receiver 23. This receiver 23 is provided with distillate draw-od' pipe 24 having throttle valve 25 and gas outlet pipe 26, having throttle valve 27. The insuiciently cracked vapors are condensed in the dephlegmator 20 and may be returned as reflux condensate to the chamber 6' by means of the pipe 28 and pump 29, or, if desired,
the reflux condensate, in whole or in part,
may be returned to the chamber 12 through the pipe 30 or, if desired, part of the reflux maybe drawn out of `the system through branch v31. In order that the reux may be handled as above stated, I provide the valves 32, 33, 34 and 35, as shown.
If desired, the uncondensible gases from the receiver 23, in Whole or in part, may be returned to the system by means of the gas line 37, having throttle valve 38, pump 39 and feed line 40; thence, from feed line 40, either to the chamber 6, through branch 41, having throttle valve 42 or to the chamber 13 throughbranch 43, having throttle valve 44. The arrangement is such that the uncondensible gases may be returned either to chamber 6 or chamber 13 or to both chambers. The oil to be treated may be crude, topped crude, fuel oil or distillates. The extent to which the cracking reaction Will take place Will vary With the kind of charging stock treated and the products desired. It Will be noted, however, that the cracking in the chamber 6 may be controlled entirely independently of the extent of the cracking that may take place in the vapor phase chamber 12 In certain cases, it may be desirable to introduce a'catalyst into the cracking chambers as, for example, iron oxide, nickel or MoneI metal. Y
I claim as my invention:
1. A process of cracking hydrocarbon oil consisting in subjecting the oil to an initial cracking step, separating the oils into vapors relatively free from coke forming constituents and into residue, isolating said residue from the process subjecting such vapors freed of said residue to a vapor phase cracking reaction as a second cracking step, in both the said steps subjecting the oil constituents to the direct physical contact action of temperature controlled combustion gases, passing the vapors from the second cracking step to a reiiux condenser, separating the suiiiciently and insuiciently cracked vapors in said refiux condenser and recracking the reflux condensate.
2. A process for cracking hydrocarbon oil consisting in subjecting the oil to an initial cracking step, separating the oils into vapors relatively free from coke forming constituents and into residue, isolating said residue from thc process, subjecting such vapors freed of said residue to a vapor phase cracking reaction as a second cracking step, in both the said steps subjecting the oil constituents to the direct action of separately temperature controlled combustion gases, passing thc vapors from the second cracking step to a reflux condenser, separating the suticiently and insuiiciently cracked vapors in said reflux condenser and recrackmg the reiux condensate, and introducing incondensible gases which have passed out of the reflux condenser back into contact with the oil being cracked.
JEAN DELATTRE SEGUY.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US244095A US1850291A (en) | 1928-01-03 | 1928-01-03 | Process of cracking oil |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US244095A US1850291A (en) | 1928-01-03 | 1928-01-03 | Process of cracking oil |
Publications (1)
Publication Number | Publication Date |
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US1850291A true US1850291A (en) | 1932-03-22 |
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Application Number | Title | Priority Date | Filing Date |
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US244095A Expired - Lifetime US1850291A (en) | 1928-01-03 | 1928-01-03 | Process of cracking oil |
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2844452A (en) * | 1950-04-05 | 1958-07-22 | Rudolph L Hasche | Self-sustaining regenerative process |
US3236763A (en) * | 1958-10-31 | 1966-02-22 | Shell Oil Co | Cracking of hydrocarbons |
-
1928
- 1928-01-03 US US244095A patent/US1850291A/en not_active Expired - Lifetime
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2844452A (en) * | 1950-04-05 | 1958-07-22 | Rudolph L Hasche | Self-sustaining regenerative process |
US3236763A (en) * | 1958-10-31 | 1966-02-22 | Shell Oil Co | Cracking of hydrocarbons |
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