US2296386A - Chemical process - Google Patents

Chemical process Download PDF

Info

Publication number
US2296386A
US2296386A US307556A US30755639A US2296386A US 2296386 A US2296386 A US 2296386A US 307556 A US307556 A US 307556A US 30755639 A US30755639 A US 30755639A US 2296386 A US2296386 A US 2296386A
Authority
US
United States
Prior art keywords
vapors
catalyst
temperature
hydrocarbons
line
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
US307556A
Inventor
Charles E Hemminger
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.)
Standard Oil Development Co
Original Assignee
Standard Oil Development Co
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 Standard Oil Development Co filed Critical Standard Oil Development Co
Priority to US307556A priority Critical patent/US2296386A/en
Priority to US309515A priority patent/US2300151A/en
Priority to GB1738/41A priority patent/GB547043A/en
Application granted granted Critical
Publication of US2296386A publication Critical patent/US2296386A/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
    • C10GCRACKING 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
    • C10G11/00Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
    • C10G11/14Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils with preheated moving solid catalysts
    • C10G11/18Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils with preheated moving solid catalysts according to the "fluidised-bed" technique
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING 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
    • C10G35/00Reforming naphtha
    • C10G35/04Catalytic reforming
    • C10G35/10Catalytic reforming with moving catalysts
    • C10G35/14Catalytic reforming with moving catalysts according to the "fluidised-bed" technique

Definitions

  • the present invention relates to improvements in the conversionV of relatively high boiling peto improvements in the catalytic cracking of relatively high boiling hydrocarbons such as gas oil in which the gas oil is at a relatively low cracking temperature during the greater portion of the time it'is undergoing cracking and thereafter is heated to a relatively high cracking temperature fora short period of time just prior to the discharge of the cracked vapors from the reaction zone to the fractionating equipment.
  • One object of the present invention is to crack relatively heavy hydrocarbons in the presence of a powdered catalyst suspended in the vaporized hydrocarbons under such conditions as to produce gasoline-like fractions in high yields.
  • a more specific object of the present invention is to carry out a catalytic cracking operation under conditions such that during the major portion of the cracking reaction the. temperatures and the time of contact are adjusted so as to minimize the formation of butane and vnormally gaseous hydrocarbons and to thereafter increase the temperature of the reaction products containing the catalyst to a sufficiently high level to cause vaporization and removal of hydrocarbons adsorbed on the catalyst.
  • Another important object of the present invention is to effect an economy with respect to the quantity of catalyst employed. That is to say, it is an important feature of the present invention to so adjust operating conditions as to enable the use of a smaller quantity of catalyst than has been heretofore employed.
  • I provide a process in which a residuum such as reduced crude is vaporized then mixed with a powdered catalyst and thereafter discharged into a reactor where the hydrocarbons are subjected' to cracking conditions. Thereafter the reaction products are discharged into a heating coil where the temperature is rapidly increased to a point suicently high to vaporize residual heavy hydrocarbons absorbed on the catalyst surface.
  • the catalyst' is separated from thehydrocarbon vapors in one or more cyclone separators or equivalent devices operating in series, regenerated and returned tothe process.
  • FIG. 1 is a diagrammatic illustration in partial vertical section of a suitable apparatus in which the present invention gravity of 21.
  • the fresh feed is discharged intov a vaporizing column 2.
  • Steam to assist in the vaporization of the fresh feed is introduced into the bottom of tower 2 through line 3.
  • the bottoms from this tower are withdrawn through line 4 and by suitable treatment may be converted into bunker fuel or some similar material.
  • the overhead product is withdrawn from tower 2 through line 5 and forced into an injector 6.
  • Fresh or regenerated catalyst is introduced into the injector 6 through line 1 where it is dispersed in the oil vapors. Steam to assist in the dispersion may be introduced into injector 6 through line 8.
  • the vapors entering injector 6 may be at a temperature of about 825 F;
  • the amount of steam which is employed is not sucient to change the temperature of the vapors and its use in the process is purely optional.
  • the catalyst which is introduced into injector 6 is at a temperature of about 1000 F. and the intermixing of the hydrocarbon vapors and the catalyst causes the-temperature of the mixture t0 attain a. value of about 875 F. when it is discharged from injector 6 into line 5.
  • The'amount of catalyst employed is preferably about 3 partsV lyst dispersed or suspended therein are dis-' charged into a reactor 9 which may be of the shell type or some suitable construction. Here in drum 9 the main cracking reaction takes place.
  • the vapors are resident in this reactor 9 for a period of time within the range of from about 15 to 150 seconds.
  • the outlet temperature of the reaction products withdrawn through line I0 is about 825 F. and at this temperature the vapors are discharged into a fired coil I I where the temperature of the vapors is increased to about 1000 F.
  • the vapors are resident in this coil Il from 3 to -10 seconds. per square inch gauge is maintained on the vapors in drum 9 while a somewhat lower pressure is maintained Ain coilA Il, say a pressure of about 10 pounds per square inch gauge.
  • the reaction products are withdrawn from coil Il through line I9 and discharged into a separating device such as a cyclone separator 20.
  • the temperature of the vapors in this cyclone' separator is about 1000 F.
  • Two or more and preferably four cyclone vseparators may be employed in series.
  • the vapors substantially freed of their catalyst content are .discharged into line 2

Landscapes

  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (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

Sept. 22, 1942.
.STEAM UNE VAPOR: z nv c COLUMN FEEDv /IYLE 7' STEAM C. E. HEMMINGER CHEMICAL PROCESS Filed Deo. 5, 1959 CATHL V57' .REGE [VERAy-QN S75 Tfr l CATA; V757'. Horpfk REAcv-ovz :e o e' FPECEI Y/NG .7971 UM Patented Sept. 22, 1942 CHEMICAL PROCESS Charles E. Hemminger, Westfield, N. J., assignor to Standard Oil Development Company, a corporation of Delaware Application December '5, 1939, serial No. 307,556
(ci. 19e- 52) 7 Claims.
The present invention relates to improvements in the conversionV of relatively high boiling peto improvements in the catalytic cracking of relatively high boiling hydrocarbons such as gas oil in which the gas oil is at a relatively low cracking temperature during the greater portion of the time it'is undergoing cracking and thereafter is heated to a relatively high cracking temperature fora short period of time just prior to the discharge of the cracked vapors from the reaction zone to the fractionating equipment.
One object of the present invention is to crack relatively heavy hydrocarbons in the presence of a powdered catalyst suspended in the vaporized hydrocarbons under such conditions as to produce gasoline-like fractions in high yields.
A more specific object of the present invention is to carry out a catalytic cracking operation under conditions such that during the major portion of the cracking reaction the. temperatures and the time of contact are adjusted so as to minimize the formation of butane and vnormally gaseous hydrocarbons and to thereafter increase the temperature of the reaction products containing the catalyst to a sufficiently high level to cause vaporization and removal of hydrocarbons adsorbed on the catalyst.
Another important object of the present invention is to effect an economy with respect to the quantity of catalyst employed. That is to say, it is an important feature of the present invention to so adjust operating conditions as to enable the use of a smaller quantity of catalyst than has been heretofore employed.
Other objects of the invention will bc apparent from the ensuing description.
In carrying the present invention into effect, I provide a process in which a residuum such as reduced crude is vaporized then mixed with a powdered catalyst and thereafter discharged into a reactor where the hydrocarbons are subjected' to cracking conditions. Thereafter the reaction products are discharged into a heating coil where the temperature is rapidly increased to a point suicently high to vaporize residual heavy hydrocarbons absorbed on the catalyst surface.
. The catalyst'is separated from thehydrocarbon vapors in one or more cyclone separators or equivalent devices operating in series, regenerated and returned tothe process.
'Ihe accompanying drawing is a diagrammatic illustration in partial vertical section of a suitable apparatus in which the present invention gravity of 21. The fresh feed is discharged intov a vaporizing column 2. Steam to assist in the vaporization of the fresh feed is introduced into the bottom of tower 2 through line 3. The bottoms from this tower are withdrawn through line 4 and by suitable treatment may be converted into bunker fuel or some similar material. The overhead product is withdrawn from tower 2 through line 5 and forced into an injector 6. Fresh or regenerated catalyst is introduced into the injector 6 through line 1 where it is dispersed in the oil vapors. Steam to assist in the dispersion may be introduced into injector 6 through line 8. The vapors entering injector 6 may be at a temperature of about 825 F; The amount of steam which is employed is not sucient to change the temperature of the vapors and its use in the process is purely optional. However, the catalyst which is introduced into injector 6 is at a temperature of about 1000 F. and the intermixing of the hydrocarbon vapors and the catalyst causes the-temperature of the mixture t0 attain a. value of about 875 F. when it is discharged from injector 6 into line 5. The'amount of catalyst employed is preferably about 3 partsV lyst dispersed or suspended therein are dis-' charged into a reactor 9 which may be of the shell type or some suitable construction. Here in drum 9 the main cracking reaction takes place. The vapors are resident in this reactor 9 for a period of time within the range of from about 15 to 150 seconds. The outlet temperature of the reaction products withdrawn through line I0 is about 825 F. and at this temperature the vapors are discharged into a fired coil I I where the temperature of the vapors is increased to about 1000 F. The vapors are resident in this coil Il from 3 to -10 seconds. per square inch gauge is maintained on the vapors in drum 9 while a somewhat lower pressure is maintained Ain coilA Il, say a pressure of about 10 pounds per square inch gauge. The reaction products are withdrawn from coil Il through line I9 and discharged into a separating device such as a cyclone separator 20. The temperature of the vapors in this cyclone' separator is about 1000 F. Two or more and preferably four cyclone vseparators may be employed in series. The vapors substantially freed of their catalyst content are .discharged into line 2| leading to fractionating tower 22 where the same are l fractionated to give an overhead product containing hydrocarbons boiling within the gasoline range and lighter hydrocarbons including normally gaseous hydrocarbons and 2% bottoms A pressure of about 15 pounds
US307556A 1939-12-05 1939-12-05 Chemical process Expired - Lifetime US2296386A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
US307556A US2296386A (en) 1939-12-05 1939-12-05 Chemical process
US309515A US2300151A (en) 1939-12-05 1939-12-16 Art of treating hydrocarbons
GB1738/41A GB547043A (en) 1939-12-05 1941-02-10 Improvements in or relating to the catalytic treatment of hydrocarbons

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US307556A US2296386A (en) 1939-12-05 1939-12-05 Chemical process

Publications (1)

Publication Number Publication Date
US2296386A true US2296386A (en) 1942-09-22

Family

ID=23190262

Family Applications (1)

Application Number Title Priority Date Filing Date
US307556A Expired - Lifetime US2296386A (en) 1939-12-05 1939-12-05 Chemical process

Country Status (2)

Country Link
US (1) US2296386A (en)
GB (1) GB547043A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2424147A (en) * 1941-05-09 1947-07-15 Standard Oil Dev Co Controlling catalyst-oil ratio by use of a venturi
US2467149A (en) * 1940-11-02 1949-04-12 Standard Oil Dev Co Handling finely divided materials

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2467149A (en) * 1940-11-02 1949-04-12 Standard Oil Dev Co Handling finely divided materials
US2424147A (en) * 1941-05-09 1947-07-15 Standard Oil Dev Co Controlling catalyst-oil ratio by use of a venturi

Also Published As

Publication number Publication date
GB547043A (en) 1942-08-11

Similar Documents

Publication Publication Date Title
US2379711A (en) Catalytic conversion of hydrocarbon oils
US2303047A (en) Catalytic treatment of hydrocarbons
US2340974A (en) Refining process
US2360622A (en) Method of producing aviation gasoline
US2598058A (en) Continuous conversion and coking of heavy liquid hydrocarbons
US2296722A (en) Cracking of hydrocarbon oils
US2437222A (en) Hydrocarbon conversion process
US2300152A (en) Art of catalytic cracking
US2353731A (en) Hydrocarbon conversion
US2312230A (en) Catalytic conversion of hydrocarbons
US2396758A (en) Catalytic conversion of hydrocarbon oils
US2300151A (en) Art of treating hydrocarbons
US2247126A (en) Clean circuit powdered catalyst cracking
US2296386A (en) Chemical process
US3732081A (en) Apparatus for fluid-solid contacting operations
US2427820A (en) Catalytic cracking process
US2322019A (en) Art of treating hydrocarbons
US2351422A (en) Cracking of hydrocarbon oil
US2398846A (en) Making gasoline
US2419519A (en) Conversion of hydrocarbons
US2428666A (en) Catalytic conversion of hydrocarbons
US2420904A (en) Conversion of hydrocarbons
US2301322A (en) Chemical process
US1860199A (en) Method of cracking hydrocarbon oils
US2305004A (en) Chemical process