US2380713A - Coking hydrocarbon oils - Google Patents

Coking hydrocarbon oils Download PDF

Info

Publication number
US2380713A
US2380713A US453783A US45378342A US2380713A US 2380713 A US2380713 A US 2380713A US 453783 A US453783 A US 453783A US 45378342 A US45378342 A US 45378342A US 2380713 A US2380713 A US 2380713A
Authority
US
United States
Prior art keywords
coking
vapors
condensate
drum
coke
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
US453783A
Inventor
Wilson Howard
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.)
Texaco Inc
Original Assignee
Texaco Inc
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 Texaco Inc filed Critical Texaco Inc
Priority to US453783A priority Critical patent/US2380713A/en
Application granted granted Critical
Publication of US2380713A publication Critical patent/US2380713A/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
    • C10BDESTRUCTIVE DISTILLATION OF CARBONACEOUS MATERIALS FOR PRODUCTION OF GAS, COKE, TAR, OR SIMILAR MATERIALS
    • C10B55/00Coking mineral oils, bitumen, tar, and the like or mixtures thereof with solid carbonaceous material

Definitions

  • the preheating of the coke drum is accomplished by utilizing asourceoiheatwhichisavailableinthe coking unit and which is independent of the thermodynamic balance of the unit.
  • vapors evolved in the coking operation are subjected to reflux condensation to produce a hot condensate which is normally withdrawn as a product of the process and which is periodically diverted to a coking drum to preheat it.
  • the vapors from the coking operation are subjected to a primary dephlegmation to produce a heavy ⁇ condensate "adapted for fuel oil.
  • the invention may be practiced in connection with various types oi coking processes.
  • hydrocarbon oil such as a petroleum residual stock is passed through a heating coil wherein itis heated toa cracking temperature and delivered to a coking drum;
  • the vapors -irom the coking drum are fractionated to obtain 'a condensate stock which is passed through a recycling cracking coil and the heated products are combined with a residual stock, the resultant mixture being delivered to the coking drum.
  • the residual stock is utilized in the dephlegmation of vapors and the resultant mixture of redux condensate and unvaporized residual stock is withdrawn from the dephlegmator and either passed through a heating coil or combined directly with the hot products from the cycle condensate cracking coil for passage to the coking drum.
  • a reaction chamber is interposed between the heating coil and the coking drum.
  • the apparatus illustrated includes a heating coil A, a reaction chamber B, cokng chambers C and D and fractionating towers E and F.
  • the heating coil A is mounted in a furnace I adapted to heat the oil therein to a cracking temperature.
  • the heated oil is directed through a transfer line II to the reaction chamber B, the heated stream of oil being combined with additional oil as is hereinafter explained.
  • the reaction chamber B is insulated against heat loss and is adapted to maintain the oil Vtherein at a cracking temperature.
  • the coking drums are insulated against heat loss and are adapted to retain the hot oil received from the reaction chamber so that it may be converted to coke autogenously. Vapors from the coking drums C and D pass through lines I8 and II, respectively, to a manifold vapor line I8 thence to the fractionating tower E.
  • the fractionating tower E is formed with a section I9, which receives the vapors from the coking operation through line I8, providing a primary dephlegmating zone for the coke still vapors, -and with a section 20 which receives the separated vapors from the reaction chamber B through the line I2 as well as the dephlegmated coke still vapors from the primary dephlegmatlng zone I9.
  • Charging stock such as crude petroleum or topped or reduced crude
  • the vapors therein are dephlegmatedwith the charging stock to form a resultant mixture of, reflux condensate and unvaporized charging stock which -is collected on a tray 22.
  • This mixture is withdrawn by a pump 23 and directed through a line 24 to the transfer line II so as to commingle the mixture with the hot products passing from the heating coil A to the reaction chamber B.
  • the vapors uncondensed in the fractionatlng zone 20 pass through a vapor line 25 to the fractionating tower F ⁇ wherein the vapors are subjected to fractionation.
  • Redux condensate is withdrawn from the tower F -by a pump 26 and directed through a line 21 to the heating coil A.
  • the overhead vapors from the tower F pass to a condenser 28 thence to a distillate accumulator or gas separator 29.
  • the vapors from the coking operation are subjected to a primary dephlegmation prior to being commingled with the vapors from the reaction chamberv B for further fractionation in fractionating zones 20 and F.
  • 'Ihis dephlegmation produces a tarry condensate product which is of relatively high specific gravity in relation to its viscosity and is particularly adapted for fuel oil.
  • this tarry condensate is normally withdrawn through a line 30 and passed either through a cooler to storage, or to a tar flasher in case'it is desired to distlll olf any contained constituents of lower boiling point than desired in the fuel product.
  • the tarry condensate passing through the line 30 is diverted to a pump3I by which the condensate is directed through a manifold line 32 thence either through branch line 33 to the coke drum C or through branch line 34 to the coke drum D.
  • the coke drums C and D may be provided with drawoi lines 35 and 36, respectively, so that a portion or all of the hot condensate introduced to a coke drum for preheating it may be withdrawn from the system. It is not necessary, however, to withdraw the oil used in the preheati'ng and in fact such oil is preferably permitted to remain in the coke drum for coking.
  • the cycle 'condensate is subjected to cracking in the coil A at temperatures such as 1000 F.l050 F. under a superatmospheric pressure such as 40G-800 lbs. and the eflluent from the heating coil is combined with a mixture of reflux condensate and residual stock for reaction in the reaction and separating chamber B wherein ⁇ 885 F. are effective coking temperatures.
  • cracking is carried on at temperatures in excess of 900 F. under superatmospheric pressure such as 30D-600 lbs. Liquid is prevented from acoumulating in the reaction chamber by the rapid withdrawal of the liquid residue together with a sufficient portion of the vapors to effect autogenous coking in one of the coking drums C or D.
  • a temperature of 910 F. in the stream of vapors and liquid passing from the reaction chamber B to the coking drum is adequate to accomplish autogenous cokin'g.
  • the pressure in the coking drum is about 50-100 lbs. or higher; Vfor example, with pressures of 350- 400 lbs. in the reaction chamber B an advantageous pressure in the coke drum is -1'75 lbs.
  • the vapors-from the coking drum are subjected to a primary dephlegmation in the dephlegmating zone I9, a relatively small amount of cooling being supplied thereto so that only the heavier components are condensed to form a heavy tarryy condensate which may be withdrawn from the dephlegmating zone at temperatures of the order of 790 F8l5 F. It is advantageous to recycle a portion of this tarry condensate through the dephlegmating zone I9 in order to increase the liquid ow therein and prevent coking.
  • the tarry condensate is normally withdrawn as a fuel oil product of the process.
  • the dephlegmated vapors from the dephlegmating zone I8 are combined with the vapors which are separately withdrawn from the reaction chamber B and the combined vapors are subjected to dephlegmation in the dephlegmating zone 20 into which charging stock such as topped or reduced crude is introduced.
  • the resultant mixture of reflux condensate and unvaporized crude residuuxn is withdrawn at temperatures such as 790 F.815 F. and combined with the heated effluent from the cracking coil 'A for cracking in the reaction chamber B.
  • the overhead vapors ⁇ from the dephlegmator 20 pass to the fractionator F at a temperature of for example '710 F.-730 F.
  • an overhead distillate such as a 400 F. end point gasoline product, and a higher boiling reflux condensate which is withdrawn at temperatures, for example, of 660 F.-680 F. and directed to the heating coll A.
  • the delivery of the condensate to the coke drum at temperatures above 750 F., and preferably approximating 800 F. serves to preheat it sufficiently that when the stream from the reaction chamber B is directed thereto there will be no material condensation and the drum may be rapidly brought to the desired coking temperature.
  • the coke drums are conveniently provided with vapor connections to the usual steaming out tank (not shown).
  • the introduction of the hot condensate from the dephlegmator I9 into the coke drum D will cause the building up of pressure therein which may be relieved through the vapor line to the steaming out tank.
  • the valve to the steaming out tank is closed and the valve in line I1 opened to permit the passage of the vapors to the dephlegmator i9.
  • the coking in drum C will have been completed and the hot products from reaction chamber B are diverted from the coke drum C to the coke drum D and the valve in the vapor line I6 is closed.
  • the coke drum C is then steamed out and cooled and the coke removed while the coking operation is carried on in the coke drum D, with the resumption of the continuous withdrawal from the system of the tarry condensate from the primary dephlegmator.
  • Coking operations are commonly conducted in cycles approximating 12 hours; that is, by switching coke drums at time, intervals of about 12 hours, and with such a cycle of operations it is found that by diverting the tarry condensate to the preheating operation for about one hour before the end of the cokingr cycle the desired preheating of the coke drum is accomplished and the removal of the coke forming constituents from the primary dephlegmator, so as to materially increase the length of time that the unit can be maintained on stream, is likewise accomplished.

Description

July 3l, 1945. H.. WILSON COKING HYDROCARBON O'IL Filed Aug. 6, 1942 lll' lll' Il' ...vm A
.In N ..10 .minus wz, ou.h mm2/ 10 v x zo..ro mm 4 rw. .653v fm. Y
v Patented Julyv 31, 1945 VHoward Wilson, Lockport, lill, asaignor to The Tens Company, New York, N. Y? a corporation oi' Delaware Application August 6, 1942, Serial No. 453,783
3 Claims. C1. 196-58) This invention relates to the cokins oi hydrocarbon oils and involves particularly certain improvements in the preheating of the coking chambers. y
.It is common'practice to conduct coking operations in continuous units having `a plurality 'oi' coking drums by continuously passing a stream of oil through a heating zone thence severally to the coking drums in succession.v When the poking operation is completed in one of the drums unit. Efforts have been made to preheat'the coke drum prior to diverting the-heated stream of oil thereto by directing the vapors from the coke drum in operation. which normally pass .to the dephlegmator' or fractionator. into the subsequent coke drum to preheat it before diverting the stream of oil to be coked thereinto. One
diiculty with this expedient is that considerable condensation of the vapors occurs in the coke drum during the prewarming period and the condensed material distills over into the dephlegmator after the ooking operation has been commenced which upsets the balance of the unit and produces a loss in light constituents.'
In accordance with my invention the preheating of the coke drum is accomplished by utilizing asourceoiheatwhichisavailableinthe coking unit and which is independent of the thermodynamic balance of the unit. In practicing the invention vapors evolved in the coking operation are subjected to reflux condensation to produce a hot condensate which is normally withdrawn as a product of the process and which is periodically diverted to a coking drum to preheat it. In a preferred method of practicing the linvention the vapors from the coking operation are subjected to a primary dephlegmation to produce a heavy`condensate "adapted for fuel oil.
' During the normal operation this condensate is withdrawn as a producto! theprooess and near the end of the cokingoperation in a' given coking drum the hot fuel oil product is directed to a subsequent coking drum serving toV preheat it mally cause coking difficulties.
prior to diverting the stream of oil for coking into such subsequent drum. In this way the coke drum is preheated without disturbing the thermodynamic equilibriumof the unit. This method of preheating the coke drum has the further .advantage of removing the very heavy residual constituents which come over into the dephlegmator` near the end of the coking cycle and which nor- In accordance with the invention these very heavy potential coke forming constituents which are evolved in the nal stages of the coking operation and which pass over with the vapors into the dephlegmator are directed into the succeeding coke drum serving to preheat itready to receive the charge for coking. The dispositionof the heavy coke forming materials in this way serves to prevent the formation of coke in the dephlegmator and actually increases the operating time in which the unit may be maintained on-stream.
The invention may be practiced in connection with various types oi coking processes. For example, in one type of operation hydrocarbon oil such as a petroleum residual stock is passed through a heating coil wherein itis heated toa cracking temperature and delivered to a coking drum; In another type of operation the vapors -irom the coking drum are fractionated to obtain 'a condensate stock which is passed through a recycling cracking coil and the heated products are combined with a residual stock, the resultant mixture being delivered to the coking drum. In some cases the residual stock is utilized in the dephlegmation of vapors and the resultant mixture of redux condensate and unvaporized residual stock is withdrawn from the dephlegmator and either passed through a heating coil or combined directly with the hot products from the cycle condensate cracking coil for passage to the coking drum. In some cases a reaction chamber is interposed between the heating coil and the coking drum. lIn any of these various methods of coking and cracking vapors evolved in the coiring operation may in accordance with the invention be subjected to dephlegmation to form For the purpose of more fully. explaining thev invention' reference is had to the accompanying y drawing which is a tical elevation illustrating apparatus adapted for practicing a particular embodiment of the invention.
The apparatus illustrated includes a heating coil A, a reaction chamber B, cokng chambers C and D and fractionating towers E and F. The heating coil A is mounted in a furnace I adapted to heat the oil therein to a cracking temperature. The heated oil is directed through a transfer line II to the reaction chamber B, the heated stream of oil being combined with additional oil as is hereinafter explained. The reaction chamber B is insulated against heat loss and is adapted to maintain the oil Vtherein at a cracking temperature. Separation of vapors from liquid components takes place in the reaction chamber B, separated vapors being passed through a vapor line I2 to the fractionating tower E and liquid residue, together with a sulcient portion of the vapors to accomplish autogenous coking, is withdrawn through a manifold line I3 having a branch I4 extending to the coking drum C and a branch I5 extending to the coking drum D.
The coking drums are insulated against heat loss and are adapted to retain the hot oil received from the reaction chamber so that it may be converted to coke autogenously. Vapors from the coking drums C and D pass through lines I8 and II, respectively, to a manifold vapor line I8 thence to the fractionating tower E.
The fractionating tower E is formed with a section I9, which receives the vapors from the coking operation through line I8, providing a primary dephlegmating zone for the coke still vapors, -and with a section 20 which receives the separated vapors from the reaction chamber B through the line I2 as well as the dephlegmated coke still vapors from the primary dephlegmatlng zone I9.
Charging stock, such as crude petroleum or topped or reduced crude, is introduced by a pump 2| to the dephlegmating section 20. The vapors therein are dephlegmatedwith the charging stock to form a resultant mixture of, reflux condensate and unvaporized charging stock which -is collected on a tray 22. This mixture is withdrawn by a pump 23 and directed through a line 24 to the transfer line II so as to commingle the mixture with the hot products passing from the heating coil A to the reaction chamber B. The vapors uncondensed in the fractionatlng zone 20 pass through a vapor line 25 to the fractionating tower F `wherein the vapors are subjected to fractionation. Redux condensate is withdrawn from the tower F -by a pump 26 and directed through a line 21 to the heating coil A. The overhead vapors from the tower F pass to a condenser 28 thence to a distillate accumulator or gas separator 29.
In the dephlegmator I9 the vapors from the coking operation are subjected to a primary dephlegmation prior to being commingled with the vapors from the reaction chamberv B for further fractionation in fractionating zones 20 and F. 'Ihis dephlegmation producesa tarry condensate product which is of relatively high specific gravity in relation to its viscosity and is particularly adapted for fuel oil. During the operation of the process this tarry condensate is normally withdrawn through a line 30 and passed either through a cooler to storage, or to a tar flasher in case'it is desired to distlll olf any contained constituents of lower boiling point than desired in the fuel product. Periodically when it is desired to preheat a coke drum,v the tarry condensate passing through the line 30 is diverted to a pump3I by which the condensate is directed through a manifold line 32 thence either through branch line 33 to the coke drum C or through branch line 34 to the coke drum D. The coke drums C and D may be provided with drawoi lines 35 and 36, respectively, so that a portion or all of the hot condensate introduced to a coke drum for preheating it may be withdrawn from the system. It is not necessary, however, to withdraw the oil used in the preheati'ng and in fact such oil is preferably permitted to remain in the coke drum for coking.
In a typical operation in accordance with the invention the cycle 'condensate is subjected to cracking in the coil A at temperatures such as 1000 F.l050 F. under a superatmospheric pressure such as 40G-800 lbs. and the eflluent from the heating coil is combined with a mixture of reflux condensate and residual stock for reaction in the reaction and separating chamber B wherein `885 F. are effective coking temperatures.
cracking is carried on at temperatures in excess of 900 F. under superatmospheric pressure such as 30D-600 lbs. Liquid is prevented from acoumulating in the reaction chamber by the rapid withdrawal of the liquid residue together with a sufficient portion of the vapors to effect autogenous coking in one of the coking drums C or D. A temperature of 910 F. in the stream of vapors and liquid passing from the reaction chamber B to the coking drum is adequate to accomplish autogenous cokin'g. The pressure in the coking drum is about 50-100 lbs. or higher; Vfor example, with pressures of 350- 400 lbs. in the reaction chamber B an advantageous pressure in the coke drum is -1'75 lbs. Temperatures of 840 F.-
The vapors-from the coking drum are subjected to a primary dephlegmation in the dephlegmating zone I9, a relatively small amount of cooling being supplied thereto so that only the heavier components are condensed to form a heavy tarryy condensate which may be withdrawn from the dephlegmating zone at temperatures of the order of 790 F8l5 F. It is advantageous to recycle a portion of this tarry condensate through the dephlegmating zone I9 in order to increase the liquid ow therein and prevent coking. The tarry condensate is normally withdrawn as a fuel oil product of the process. The dephlegmated vapors from the dephlegmating zone I8 are combined with the vapors which are separately withdrawn from the reaction chamber B and the combined vapors are subjected to dephlegmation in the dephlegmating zone 20 into which charging stock such as topped or reduced crude is introduced. The resultant mixture of reflux condensate and unvaporized crude residuuxn is withdrawn at temperatures such as 790 F.815 F. and combined with the heated effluent from the cracking coil 'A for cracking in the reaction chamber B. The overhead vapors `from the dephlegmator 20 pass to the fractionator F at a temperature of for example '710 F.-730 F. and the vapors are fractionated to obtain an overhead distillate, such as a 400 F. end point gasoline product, and a higher boiling reflux condensate which is withdrawn at temperatures, for example, of 660 F.-680 F. and directed to the heating coll A.
Assuming that the -coking operation is being carried on in the coke drum C it will be desired to preheat the coke drum D near the end of the coking operation in coke drum C at which time extremely heavy potential coke forming constituents are evolved from the coking drum and passed through the vapor line to 'the primary dephlegmating zone. The hot tarry distillate which normally is being'withdrawn from the system is then diverted to the coke drum D. Inv this way the heavy coke forming constituents are flushed out of the primary ydephlegmator and utilized to preheat the coke drum D. It is generally preferable 4to completely drain the liquid in the bottom of the dephlegmator so as to insure the removal of the heavy potential coke forming constituents. The delivery of the condensate to the coke drum at temperatures above 750 F., and preferably approximating 800 F. serves to preheat it sufficiently that when the stream from the reaction chamber B is directed thereto there will be no material condensation and the drum may be rapidly brought to the desired coking temperature.
The coke drums are conveniently provided with vapor connections to the usual steaming out tank (not shown). The introduction of the hot condensate from the dephlegmator I9 into the coke drum D will cause the building up of pressure therein which may be relieved through the vapor line to the steaming out tank. When the pressure begins to drop the valve to the steaming out tank is closed and the valve in line I1 opened to permit the passage of the vapors to the dephlegmator i9. In the meantime the coking in drum C will have been completed and the hot products from reaction chamber B are diverted from the coke drum C to the coke drum D and the valve in the vapor line I6 is closed. The coke drum C is then steamed out and cooled and the coke removed while the coking operation is carried on in the coke drum D, with the resumption of the continuous withdrawal from the system of the tarry condensate from the primary dephlegmator.
Coking operations are commonly conducted in cycles approximating 12 hours; that is, by switching coke drums at time, intervals of about 12 hours, and with such a cycle of operations it is found that by diverting the tarry condensate to the preheating operation for about one hour before the end of the cokingr cycle the desired preheating of the coke drum is accomplished and the removal of the coke forming constituents from the primary dephlegmator, so as to materially increase the length of time that the unit can be maintained on stream, is likewise accomplished.
While I have described a particular embodiment of my invention for purposes of illustration, it should be understood that various modications and adaptations thereof which will be obvious to one skilled in the art, maybe made within the spirit of the invention as set forth in the appended claims.
Iclaim:
1. In a process wherein hydrocarbon oil is subjected to coking by the delivery of heated oil to a plurality of coking chambers successively, the process that comprises delivering a stream of heated oil to a given coking chamber and subjecting the contents thereof to coking, passing the resultant evolved vapors from said coking chamber to a dephlegmating zone wherein the vapors are subjected to a separate primary dephlegmation at high temperatures and in the absence of residual charging stock to produce a pool of tarry condensate adapted for fuel oil, normally withdrawing tarry condensate from said pool as a product of the process, diverting said tarry condensate near the end of the coking cycle in said cokingchamber to another of the coking chambers to thereby preheat such coking chamber, substantially completely draining the poolv of tarry condensate from the dephlegmating zone during such period of diversion to effect removal therefrom of heavyrv coke-forming constituents, then divertingv said stream of heated oil to the preheated cokingchamber and subjecting the contents 'thereof to coking, passing the resultant evolved vapors to the dephlegmating zone and resuming the normal withdrawal of tarry condensate from the system.
2. In a process wherein hydrocarbon oil is subjected to coking by thedelivery of heated oil to a plurality of coking chambers successively, the process that comprises delivering a stream of heated oil to a given coking chamber wherein the contents are subjected to autogenous coking, passing the resultant evolved vapors from said coking chamber to a dephlegmating zone wherein the vapors are subjected to a separate primary dephlegmation at high temperatures and in the absence of residual charging stock to produce a tarry condensate collecting at temperatures approximating 800 F. and adapted for fuel oil, normally withdrawing the tarry condensate as a product of the process, diverting said tarry condensate near the end of the coking cycle in vsaid coking chamber to another of the coking chambers to thereby preheat such coking chamber, substantially completely draining the pool of tarry condensate from the dephlegmating zone during such period of diversion to eiect removal therefrom of heavy coke-forming constituents, then diverting said stream of heated oil to the preheated coking chamber rand subjecting the contents thereof to coking, passing the resultant evolved vapors to the dephlegmating zone and resuming the normal Withdrawal of tarry condensate from the system.
3. In a cracking and coking process wherein 40 hydrocarbon oil is subjected to coking by the delivery of heated oil to a plurality of coking chambers successively, the process that comprises passing condensate oil through a heating zone wherein it is subjected to cracking temperature, combining the resultant heated products with oil as hereinafter specified for cracking in a reaction chamber, maintaining cracking temperature under superatmospheric pressure in said reaction chamber and separating vapors from liquid residue therein, directing residual constituents from the reaction chamber to a given coking chamber wherein the contents are subjected to coking, passing the resultant evolved vapors from said coking chamber to a primary dephlegmating zone wherein said vapors are subjected to a separate primary dephlegmation at high temperatures and in the absence of residual charging stock to produce a tarry condensate constituting a synthetic fuel oil, normally withdrawing the'synthetic fuel oil as a product of the process, passing the resultant dephlegmated vapors and the separated vapors from said reaction chamber to a second dephlegmating Zone wherein the vapors are dephlegmated with charging stock, utilizing the resultant mixture of reflux condensate and unvaporized charging stock as the oil being combined with the heated products from said heating zone, subjecting the vapors from the second dephlegmating Zone to further fractionation to separate a reflux condensate from lighter products, recycling said reflux condensate to the heating zone, near the end of the coking cycle in said coking chamber diverting the synthetic fuel oil being withdrawn from said primary dephlegmating zone to another of the coking chambers to from the reaction chamber to the preheated coking chamber and subjecting the contents thereof to coking, passing the resultant evolved vapors to the dephlegmating zone and resuming the normal withdrawal of tarry condensate from the 5 system.
HOWARD WILSON.
US453783A 1942-08-06 1942-08-06 Coking hydrocarbon oils Expired - Lifetime US2380713A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US453783A US2380713A (en) 1942-08-06 1942-08-06 Coking hydrocarbon oils

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US453783A US2380713A (en) 1942-08-06 1942-08-06 Coking hydrocarbon oils

Publications (1)

Publication Number Publication Date
US2380713A true US2380713A (en) 1945-07-31

Family

ID=23802043

Family Applications (1)

Application Number Title Priority Date Filing Date
US453783A Expired - Lifetime US2380713A (en) 1942-08-06 1942-08-06 Coking hydrocarbon oils

Country Status (1)

Country Link
US (1) US2380713A (en)

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3472761A (en) * 1967-03-28 1969-10-14 Continental Oil Co Process for the manufacture of two or more grades of petroleum coke
US4518487A (en) * 1983-08-01 1985-05-21 Conoco Inc. Process for improving product yields from delayed coking
US4519898A (en) * 1983-05-20 1985-05-28 Exxon Research & Engineering Co. Low severity delayed coking
US4534854A (en) * 1983-08-17 1985-08-13 Exxon Research And Engineering Co. Delayed coking with solvent separation of recycle oil
EP0200786A1 (en) * 1984-10-25 1986-11-12 Koa Oil Company, Limited Coking apparatus
US4661241A (en) * 1985-04-01 1987-04-28 Mobil Oil Corporation Delayed coking process
US4797197A (en) * 1985-02-07 1989-01-10 Mallari Renato M Delayed coking process
US4853106A (en) * 1987-08-19 1989-08-01 Mobil Oil Corporation Delayed coking process
US8894841B2 (en) 2011-07-29 2014-11-25 Saudi Arabian Oil Company Solvent-assisted delayed coking process
US9023193B2 (en) 2011-05-23 2015-05-05 Saudi Arabian Oil Company Process for delayed coking of whole crude oil
US9574143B2 (en) 2010-09-07 2017-02-21 Saudi Arabian Oil Company Desulfurization and sulfone removal using a coker
US10093870B2 (en) 2010-09-07 2018-10-09 Saudi Arabian Oil Company Desulfurization and sulfone removal using a coker
US10093871B2 (en) 2010-09-07 2018-10-09 Saudi Arabian Oil Company Desulfurization and sulfone removal using a coker

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3472761A (en) * 1967-03-28 1969-10-14 Continental Oil Co Process for the manufacture of two or more grades of petroleum coke
US4519898A (en) * 1983-05-20 1985-05-28 Exxon Research & Engineering Co. Low severity delayed coking
US4518487A (en) * 1983-08-01 1985-05-21 Conoco Inc. Process for improving product yields from delayed coking
US4534854A (en) * 1983-08-17 1985-08-13 Exxon Research And Engineering Co. Delayed coking with solvent separation of recycle oil
EP0200786A1 (en) * 1984-10-25 1986-11-12 Koa Oil Company, Limited Coking apparatus
EP0200786A4 (en) * 1984-10-25 1987-03-30 Koa Oil Co Ltd Coking apparatus.
US4797197A (en) * 1985-02-07 1989-01-10 Mallari Renato M Delayed coking process
US4661241A (en) * 1985-04-01 1987-04-28 Mobil Oil Corporation Delayed coking process
US4853106A (en) * 1987-08-19 1989-08-01 Mobil Oil Corporation Delayed coking process
US9574143B2 (en) 2010-09-07 2017-02-21 Saudi Arabian Oil Company Desulfurization and sulfone removal using a coker
US10093870B2 (en) 2010-09-07 2018-10-09 Saudi Arabian Oil Company Desulfurization and sulfone removal using a coker
US10093871B2 (en) 2010-09-07 2018-10-09 Saudi Arabian Oil Company Desulfurization and sulfone removal using a coker
US9023193B2 (en) 2011-05-23 2015-05-05 Saudi Arabian Oil Company Process for delayed coking of whole crude oil
US8894841B2 (en) 2011-07-29 2014-11-25 Saudi Arabian Oil Company Solvent-assisted delayed coking process

Similar Documents

Publication Publication Date Title
US2380713A (en) Coking hydrocarbon oils
US2149860A (en) Conversion of hydrocarbon oils
US2198557A (en) Cracking hydrocarbon oils
US2316334A (en) Cracking hydrocarbon oils
US2036968A (en) Treatment of hydrocarbon oils
US2126204A (en) Conversion of hydrocarbon oils
US2075599A (en) Conversion and coking of hydrocarbon oils
US2361891A (en) Conversion of hydrocarbon oils
US2107793A (en) Conversion of hydrocarbon oils
US2203025A (en) Conversion of hydrocarbon oils
US2219521A (en) Conversion of hydrocarbon oils
US1969772A (en) Treatment of hydrocarbon oils and coal
US2223192A (en) Conversion of hydrocarbon oils
US2079148A (en) Conversion of hydrocarbon oils
US2167507A (en) Conversion of hydrocarbon oils
US2050467A (en) Treatment of hydrocarbon oil
US2127011A (en) Conversion of hydrocarbon oils
US2127014A (en) Conversion of hydrocarbon oils
US2109640A (en) Conversion of hydrocarbon oils
US2130407A (en) Conversion of hydrocarbon oils
US2088778A (en) Cracking hydrocarbon oils
US1949486A (en) Treatment of hydrocarbon oil
US2130436A (en) Conversion of hydrocarbon oils
US2254551A (en) Conversion of hydrocarbon oils
US2055085A (en) Treatment of hydrocarbon oil