US2061833A - Treatment of hydrocarbon oils - Google Patents

Treatment of hydrocarbon oils Download PDF

Info

Publication number
US2061833A
US2061833A US590034A US59003432A US2061833A US 2061833 A US2061833 A US 2061833A US 590034 A US590034 A US 590034A US 59003432 A US59003432 A US 59003432A US 2061833 A US2061833 A US 2061833A
Authority
US
United States
Prior art keywords
heating element
conversion
line
coking
valve
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
US590034A
Inventor
Egloff Gustav
Fisher Alfred
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.)
Universal Oil Products Co
Original Assignee
Universal Oil Products 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 Universal Oil Products Co filed Critical Universal Oil Products Co
Priority to US590034A priority Critical patent/US2061833A/en
Application granted granted Critical
Publication of US2061833A publication Critical patent/US2061833A/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
    • C10G9/00Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
    • C10G9/34Thermal 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
    • C10G9/36Thermal 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

Definitions

  • This invention relates to the treatment of hydrocarbon oils and more particularly refers to the conversion of relatively heavy oils with simultaneous reduction of the residual conversion prod- 5 nets to substantially devolatilized coke.
  • the present invention offers an improved method and means of attaining continuous extensive conversion of relatively heavy hydrocarbon oils and simultaneous low pressure continuous coking of the residual products of conversion in the single system. Provision is made for conversion of the charging stock and, when desired, conversion of intermediate and/or end products of the primary conversion at substantial superatmospheric pressure thus insuring the production of maximum yields of light products of the desired quality. At the same time the invention provides for continuous coking of the residual conversion products at low pressure or under partial vacuum which insures the recovery of maximum yields of lighter products and substantial devolatilization of the carbonaceous residue.
  • the heat required for the desired degree of conversion of the raw oil charging stock need be supplied thereto during its passage through the heating element, all or a substantial portion of the heat required to complete coking of the residual products and devolatilization of the coke being supplied to a heat carrying medium which may comprise any desired intermediate product or light end product of the system or combinations thereof.
  • a heat carrying medium which may comprise any desired intermediate product or light end product of the system or combinations thereof.
  • One specific embodiment of the invention may comprise subjecting a hydrocarbon oil to conversion at substantial super-atmospheric pressure in a heating element, introducing the heated material into a coking chamber operated at sub stantially atmospheric or subatmospheric pressure, subjecting vapors from the coking chamber to fractionation, subjecting reflux condensate from the iractionator to more severe conversion conditions at substantial superatmospheric pressure in a separate heating element and introducing the heated materials into direct contact with the residual conversion products in the coking chamber to assist their reduction to coke and eflect its substantial devolatilization, subjecting vaporous products from the fractionator to condensation and collecting the resulting distillate and uncondensable gas.
  • distillate or uncondensable gas or both may be supplied to said separate heating element 5 where they may be subjected to conversion or reforming, serving as a portion or all of the heat carrying medium supplied, as described, to the coking chamber.
  • reflux 10 condensate from the fractionator may be withdrawn from the system, may be supplied together with the distillate and/or gas to the separate heating element for further conversion, or it may be returned to the heating element to 5 which the raw oil charging stock is supplied.
  • Raw oil charging stock may be supplied through line I and valve 2 to pump 3 from which it is fed through line 4 and valve 5 to heating element 6 which is disposed within a furnace l of any suitable form wherein the oil is heated to the desired conversion temperature preferably at substantial superatmospheric pressure. 30
  • the heated oil is discharged from heating element 6 through line 8 and may pass through line 9 and valve l0 into coking chamber II or through line 9' and valve l0 into coking chamber ll.
  • Chambers H and H are similar coking zones preferably operated at substantially atmospheric or sub-atmospheric pressure wherein coking of the residual conversion products and substantial devolatilization of the coke is accomplished. It will be understood that only one coking chamber or any number of a plurality of such zones may be employed, a plurality of such zones operated alternately being preferred although simultaneous operation may be employed, if desired.
  • Vapors from chamber II are withdrawn through line l2 and valve [3 while vapors from chamber II are withdrawn through line I2 and valve l3. Said vapors thence pass through line H to fractionator l5 wherein their relatively light and relatively heavy components are separated, the latter condensing as reflux condensate and collecting in the lower portion of the fractionator while the former are withdrawn through line l6 and valve H, are subjected to condensatillate may be removed from the receiver through line 29 and valve 30.
  • Reflux condensate accumulating in the lower portion of fractionator I5 is withdrawn through line 3
  • a portion or all of the reflux condensate may be directed through line 34 and valve 35 to pump 36 from which it may be directed, all or in part, either through line 31, valve 38 and line 4 to heating element 6 for further conversion together with the raw oil charging stock, or through line 39 and valve 40 to heating element 4
  • a portion of uncondensable gas from the receiver of the system may be directed through line 42, valve 43, pump or compressor 44, line 45, valve 45 and line 39 to heating element 4
  • a portion or all of the distillate may likewise be withdrawn from receiver 2
  • any one, any combination orall of the materials mentioned may be supplied to heating element 4
  • said .reflux condensate from the fractionator of the system is preferably supplied to heating element 4
  • conversion and coking conditions may be so controlled as to permit the removal of the product of the desired nature as reflux condensate from the fractionator.
  • regulated portions thereof may be withdrawn from the receiver and subjected to reforming conditions in heating element 4
  • Distillate may also, when desired, be blended with the reflux condensate supplied to heating element 4
  • Uncondensable gas from the receiver of the system, alone or together with distillate, may also be supplied to heating element 4
  • a portion or all of the distillate produced and, when desired, a portion of gas may be recycled to heating element 4
  • is located in a furnace 52 of any suitable form capable of heating the material supplied thereto to the desired conversion conditions which may range, for example, from conversion and refonning conditions of the order of 900 to 1050 F., and substantial super-atmospheric pressure to gas-making conditions employing temperatures as high as 1800 F. or more, and preferably atmospheric or relatively low superatmospheric pressure or even, when desired, partial vacuum.
  • are discharged through line 53, entering coking chamber ll through line 54 and valve 55 or entering coking chamber through line 54' and valve 55. Temperatures of the order of 800 to 950 F.
  • the coking zone is preferably operated at a pressure ranging from sub-atmospheric to relatively low super-atmos pheric pressure not exceeding, for example, 50 pounds or thereabouts per square inch.
  • This operation may yield, per barrel of charging stock, about 65% of material of motor fuel boiling range having an anti-knock value equivalent to an octane number of approximately 72.
  • the additional products of the system may be, per barrel of charging stock, approximately 88 pounds of coke having a volatile content of less than 10% and'about 700 cubic feet of uncondensable gas.
  • its anti-knock value may be increased to an octane number of or better, in which case the quantity and volatility of the coke will not be materially afl'ected but the gas production will be somewhat increased at the expense of the yield of distillate.
  • the charging stock is subjected, in the primary heating element, to a temperature of about 800 F. under a superatmospheric pressure of approximately 150 pounds per square inch. Slight sub-atmospheric pressure is employed in the coking chambers and substantially all of the distillate produced is subjected, together with .aportion of the gas to a temperature of approximately 1600 F. at substantially atmospheric pressure in the secondary heating element. Reflux condensate is withdrawn from the system.
  • This operation may yield approximately 120 pounds of coke having a volatile content of less than 4%, about 2700 cubic feet of gas having a calorific value of approximately 1000 B. t. u. per cubic foot and in addition about 30%, based on the charging stock, of reflux condensate suitable as premium motor fuel or for use as cracking stock, may be produced.
  • a cracking and coking process which comprises heating hydrocarbon oil to cracking temperature under super-atmospheric pressure while flowing ,in a restricted stream through a heating zone, subsequently reducing the pressure on such heated oil and introducing the same to an enlarged coking zone, separating vapors from unvaporized oil and distilling the latter to coke in the coking zone, fractionating the vapors to condense fractions thereof heavier than gasoline, separately condensing gasoline vapors uncondensed by said fractionation, combining a substantial portion of the separately condensed gasoline with reflux condensate formed by the fractionation and heating the resultant mixture in a second heating zone to higher conversion temperature than the oil in the first-mentioned heating zone, and subsequently introducing the thus heated mixture into the coking zone to assist the reduction of the un- 20 GUSTAV EGLOFF.
  • ALFRED FISHER ALFRED FISHER.

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)
  • Coke Industry (AREA)

Description

Nov. 24; 1936. G. EGLOFF ET AL TREATMENT OF HYDROCARBON OILS Filed Feb. 1, 1932 KumZunZOU flllllll l INVENTORS GUSTAV EGLOFF ALFRED FISHER M w W Patented Nov. 24, 1936 UNITED STATES PATENT OFFICE Gustav Eglofl. and Alfre d Fisher, Chicago, 111.,
assignors, by mesne assignments, to Universal Oil Products Company, tion of Delaware Chicago, 111., a corpora- Application February 1, 1932, Serial No. 590,034
1 Claim. (C
This invention relates to the treatment of hydrocarbon oils and more particularly refers to the conversion of relatively heavy oils with simultaneous reduction of the residual conversion prod- 5 nets to substantially devolatilized coke.
The present invention offers an improved method and means of attaining continuous extensive conversion of relatively heavy hydrocarbon oils and simultaneous low pressure continuous coking of the residual products of conversion in the single system. Provision is made for conversion of the charging stock and, when desired, conversion of intermediate and/or end products of the primary conversion at substantial superatmospheric pressure thus insuring the production of maximum yields of light products of the desired quality. At the same time the invention provides for continuous coking of the residual conversion products at low pressure or under partial vacuum which insures the recovery of maximum yields of lighter products and substantial devolatilization of the carbonaceous residue.
In accordance with the invention, only the heat required for the desired degree of conversion of the raw oil charging stock need be supplied thereto during its passage through the heating element, all or a substantial portion of the heat required to complete coking of the residual products and devolatilization of the coke being supplied to a heat carrying medium which may comprise any desired intermediate product or light end product of the system or combinations thereof. In this manner deposition of coke or carbonaceous material in the heating element is avoided while the additional heat required is imparted to products of the system which it is desired to further convert or reform.
One specific embodiment of the invention may comprise subjecting a hydrocarbon oil to conversion at substantial super-atmospheric pressure in a heating element, introducing the heated material into a coking chamber operated at sub stantially atmospheric or subatmospheric pressure, subjecting vapors from the coking chamber to fractionation, subjecting reflux condensate from the iractionator to more severe conversion conditions at substantial superatmospheric pressure in a separate heating element and introducing the heated materials into direct contact with the residual conversion products in the coking chamber to assist their reduction to coke and eflect its substantial devolatilization, subjecting vaporous products from the fractionator to condensation and collecting the resulting distillate and uncondensable gas.
As a modification of the above specific embodiment, distillate or uncondensable gas or both may be supplied to said separate heating element 5 where they may be subjected to conversion or reforming, serving as a portion or all of the heat carrying medium supplied, as described, to the coking chamber. In case distillate and/or uncondensable gas is utilized, as described, reflux 10 condensate from the fractionator may be withdrawn from the system, may be supplied together with the distillate and/or gas to the separate heating element for further conversion, or it may be returned to the heating element to 5 which the raw oil charging stock is supplied.
One specific form of apparatus in which the process of the present invention may be practiced, is illustrated in the attached diagrammatic drawing and a description of the drawing-embracing a description of the process of the invention, as it may be practiced in the apparatus illustrated, follows.
Raw oil charging stock may be supplied through line I and valve 2 to pump 3 from which it is fed through line 4 and valve 5 to heating element 6 which is disposed within a furnace l of any suitable form wherein the oil is heated to the desired conversion temperature preferably at substantial superatmospheric pressure. 30 The heated oil is discharged from heating element 6 through line 8 and may pass through line 9 and valve l0 into coking chamber II or through line 9' and valve l0 into coking chamber ll.
Chambers H and H are similar coking zones preferably operated at substantially atmospheric or sub-atmospheric pressure wherein coking of the residual conversion products and substantial devolatilization of the coke is accomplished. It will be understood that only one coking chamber or any number of a plurality of such zones may be employed, a plurality of such zones operated alternately being preferred although simultaneous operation may be employed, if desired.
Vapors from chamber II are withdrawn through line l2 and valve [3 while vapors from chamber II are withdrawn through line I2 and valve l3. Said vapors thence pass through line H to fractionator l5 wherein their relatively light and relatively heavy components are separated, the latter condensing as reflux condensate and collecting in the lower portion of the fractionator while the former are withdrawn through line l6 and valve H, are subjected to condensatillate may be removed from the receiver through line 29 and valve 30.
Reflux condensate accumulating in the lower portion of fractionator I5 is withdrawn through line 3| and may be discharged, all or in part, from the system through line 32 and valve 33, a suitable pump, not illustrated, being employed in case sub-atmospheric pressure is employed in the fractionator. When desired, instead of being withdrawn from the system, a portion or all of the reflux condensate may be directed through line 34 and valve 35 to pump 36 from which it may be directed, all or in part, either through line 31, valve 38 and line 4 to heating element 6 for further conversion together with the raw oil charging stock, or through line 39 and valve 40 to heating element 4| for separate treatment.
In a similar manner a portion of uncondensable gas from the receiver of the system may be directed through line 42, valve 43, pump or compressor 44, line 45, valve 45 and line 39 to heating element 4|. A portion or all of the distillate may likewise be withdrawn from receiver 2| through line 41 and valve 48 to pump 49 to be fed therefrom through line 50, valve 5| and line 39 to heating element 4|.
It will be understood that, depending primarily upon the nature of the charging stock, the operating conditions employed and the desired results, any one, any combination orall of the materials mentioned may be supplied to heating element 4| in the manner described. When the reflux condensate formed is of relatively light nature and the process is operated for the production of maximum yields of light distillate such as, for example, motor fuel of high anti-knock value, said .reflux condensate from the fractionator of the system is preferably supplied to heating element 4| where it is subjected to more severe conversion conditions than those to which the raw oil charging stock is subjected in heating element 6. When substantial yields of intermediate liquid products such as good quality fuel I oil or cracking stock are desired, conversion and coking conditions may be so controlled as to permit the removal of the product of the desired nature as reflux condensate from the fractionator. When it is desired to reform the distillate produced, regulated portions thereof may be withdrawn from the receiver and subjected to reforming conditions in heating element 4|. Distillate may also, when desired, be blended with the reflux condensate supplied to heating element 4| for the purpose of diluting this material, in which case the conversion conditions employed in heating element 4| are not necessarily sufficiently severe to involve any substantial conversion or reforming of the distillate. Uncondensable gas from the receiver of the system, alone or together with distillate, may also be supplied to heating element 4| together with reflux condensate, in which case some recombination of light gaseous hydrocarbons and heavier liquids may take place under the conditions employed in heating element 4|. In case the process is operated for the production of high yields of gas a portion or all of the distillate produced and, when desired, a portion of gas may be recycled to heating element 4| for further conversion in which case reflux condensate, if not withdrawn from the system, is preferably returned to'heating element 6 but may, when desired, be supplied all or in part, to heating element 4|.
Heating element 4| is located in a furnace 52 of any suitable form capable of heating the material supplied thereto to the desired conversion conditions which may range, for example, from conversion and refonning conditions of the order of 900 to 1050 F., and substantial super-atmospheric pressure to gas-making conditions employing temperatures as high as 1800 F. or more, and preferably atmospheric or relatively low superatmospheric pressure or even, when desired, partial vacuum. The heated materials from heating element 4| are discharged through line 53, entering coking chamber ll through line 54 and valve 55 or entering coking chamber through line 54' and valve 55. Temperatures of the order of 800 to 950 F. and substantial super-atmospheric pressures of the order of 100 to 500 pounds per square inch, or more, are preferably employed in the heating element to which the raw oil charging stock is supplied. Temperatures of the order of 900 to 1050 F. and substantial superatmospheric pressures of the order of 100 to 800 pounds or more per square inch are preferably employed in the secondary heating element of the system when the substantial recovery of light liquid products is desired. For gas-making purposes, higher temperatures of the order of 1000 to 1800* F. and sub-atmospheric to relatively low superatmospheric pressures are preferably employed in the secondary heating element. The coking zone is preferably operated at a pressure ranging from sub-atmospheric to relatively low super-atmos pheric pressure not exceeding, for example, 50 pounds or thereabouts per square inch.
As a specific example of the operation of the process of the present invention utilizing as charging stock a 25 A. P. 'I. gravity Mid-Conti nent fuel oil; this material is subjected in the primary heating element to a temperature of approximately 900" F. under a super-atmospheric pressure of approximately 250 pounds per square inch. Reflux condensate from the fractionator of the system is subjected, in the secondary heating element, to a temperature of approximately 950 F., under a. super-atmospheric pressure of approx- -imately 500 pounds per square inch. The coking chambers are operated under a slight sub-atmospheric pressure. This operation may yield, per barrel of charging stock, about 65% of material of motor fuel boiling range having an anti-knock value equivalent to an octane number of approximately 72. The additional products of the system may be, per barrel of charging stock, approximately 88 pounds of coke having a volatile content of less than 10% and'about 700 cubic feet of uncondensable gas.
By recirculating a portion of the distillate product to the secondary heating element, in an operation such as above described, its anti-knock value may be increased to an octane number of or better, in which case the quantity and volatility of the coke will not be materially afl'ected but the gas production will be somewhat increased at the expense of the yield of distillate.
As an example of another type of operation, utilizing as charging stock a poor quality of residual oil of about 12 A. P. I. gravity, the charging stock is subjected, in the primary heating element, to a temperature of about 800 F. under a superatmospheric pressure of approximately 150 pounds per square inch. Slight sub-atmospheric pressure is employed in the coking chambers and substantially all of the distillate produced is subjected, together with .aportion of the gas to a temperature of approximately 1600 F. at substantially atmospheric pressure in the secondary heating element. Reflux condensate is withdrawn from the system. This operation may yield approximately 120 pounds of coke having a volatile content of less than 4%, about 2700 cubic feet of gas having a calorific value of approximately 1000 B. t. u. per cubic foot and in addition about 30%, based on the charging stock, of reflux condensate suitable as premium motor fuel or for use as cracking stock, may be produced.
The foregoing examples illustrate only afew of the many types of operation to which the process of the present inventionis applicable and are not intended to limit the invention with respect to either operating conditions or results.
vaporized oil to coke therein.
We claim as our invention:
A cracking and coking process which comprises heating hydrocarbon oil to cracking temperature under super-atmospheric pressure while flowing ,in a restricted stream through a heating zone, subsequently reducing the pressure on such heated oil and introducing the same to an enlarged coking zone, separating vapors from unvaporized oil and distilling the latter to coke in the coking zone, fractionating the vapors to condense fractions thereof heavier than gasoline, separately condensing gasoline vapors uncondensed by said fractionation, combining a substantial portion of the separately condensed gasoline with reflux condensate formed by the fractionation and heating the resultant mixture in a second heating zone to higher conversion temperature than the oil in the first-mentioned heating zone, and subsequently introducing the thus heated mixture into the coking zone to assist the reduction of the un- 20 GUSTAV EGLOFF. ALFRED FISHER.
US590034A 1932-02-01 1932-02-01 Treatment of hydrocarbon oils Expired - Lifetime US2061833A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US590034A US2061833A (en) 1932-02-01 1932-02-01 Treatment of hydrocarbon oils

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US590034A US2061833A (en) 1932-02-01 1932-02-01 Treatment of hydrocarbon oils

Publications (1)

Publication Number Publication Date
US2061833A true US2061833A (en) 1936-11-24

Family

ID=24360625

Family Applications (1)

Application Number Title Priority Date Filing Date
US590034A Expired - Lifetime US2061833A (en) 1932-02-01 1932-02-01 Treatment of hydrocarbon oils

Country Status (1)

Country Link
US (1) US2061833A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2761825A (en) * 1951-12-04 1956-09-04 Sinclair Refining Co Fluidized coking
US4501654A (en) * 1983-11-17 1985-02-26 Exxon Research & Engineering Co. Delayed coking process with split fresh feed and top feeding

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2761825A (en) * 1951-12-04 1956-09-04 Sinclair Refining Co Fluidized coking
US4501654A (en) * 1983-11-17 1985-02-26 Exxon Research & Engineering Co. Delayed coking process with split fresh feed and top feeding

Similar Documents

Publication Publication Date Title
US2061833A (en) Treatment of hydrocarbon oils
US2018699A (en) Conversion of hydrocarbon oils
US1963264A (en) Conversion of hydrocarbon oil
US1995005A (en) Treatment of hydrocarbon oils
US2017836A (en) Conversion and coking of hydrocarbons
US2070294A (en) Treatment of hydrocarbon oils
US2098033A (en) Conversion and coking of hydrocarbons
US2089668A (en) Conversion of hydrocarbon oils
US2127013A (en) Conversion of hydrocarbon oils
US2276249A (en) Conversion of hydrocarbon oils
US1989731A (en) Conversion of hydrocarbon oils
US2048986A (en) Conversion and coking of hydrocarbon oils
US2079148A (en) Conversion of hydrocarbon oils
US2127011A (en) Conversion of hydrocarbon oils
US2009119A (en) Conversion of hydrocarbon oil
US2081348A (en) Conversion of hydrocarbon oils
US2004223A (en) Process for the conversion or cracking of high boiling hydrocarbon oils into low boiling hydrocarbon oils
US1983688A (en) Treatment of hydrocarbon oils
US1982462A (en) Hydrocarbon oil conversion
US1992299A (en) Treatment of hydrocarbon oils
US2188363A (en) Treatment of hydrocarbons
US2126988A (en) Conversion of hydrocarbon oils
US2095952A (en) Conversion of hydrocarbon oils
US1884887A (en) Treatment of hydrocarbon oils
US1939282A (en) Hydrocarbon oil conversion