US1989731A - Conversion of hydrocarbon oils - Google Patents

Conversion of hydrocarbon oils Download PDF

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US1989731A
US1989731A US613875A US61387532A US1989731A US 1989731 A US1989731 A US 1989731A US 613875 A US613875 A US 613875A US 61387532 A US61387532 A US 61387532A US 1989731 A US1989731 A US 1989731A
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conversion
chamber
oil
vapors
zone
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US613875A
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Marion W Barnes
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Universal Oil Products Co
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Universal Oil Products Co
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    • 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
    • C10G9/14Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils in pipes or coils with or without auxiliary means, e.g. digesters, soaking drums, expansion means

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  • This invention relates to the conversion of hysystem are condensed and separated into a heavy dr'ocarbon oils and more particularly refers to an fraction, containing any coke-forming residual improved process and apparatus especially adaptmaterial carried over with the vapors from the ed to the conversion of relatively heavy oils to flash distilling operation, and lower boiling frac- 5 produce maximum yields of light distillate prodtions, subjecting said lower boiling fractions of 5 ucts, such as motor fuel of high anti-knock value, the reflux condensate to conversion temperature and a residual product of controlled quality.
  • Heating coil 1 is located within a furnace 2 of 35
  • the above mentioned troubles are elimzone is heated to the desired conversion temperinated as neither the raw oil charging stock or ature preferably at substantial superatmospheric the heavy components of the reflux condensate pressure and is discharged through line 3 and pass through the high temperature heating coil valve 4 into reaction chamber 5 which is also 40 wherein the lighter reflux condensate is subjected preferably maintained at substantial superatmosto further conversion.
  • This practice permits the pheric pressure.
  • sidual liquid is withdrawn from the reaction '50 may comprise subjecting vapors resulting from chamber through line 6 and valve 7 to further 5 the conversion of hydrocarbon oil and subsequent vaporization in vaporizing or flash distilling flash distillation of the residual liquid conversion chamber 8 and vaporous conversion products may products to fractionation whereby the compoeither be withdrawn together with the residual nents of the vapors boiling above the end boiling liquid to chamber 8, in the manner described, or
  • Raw oil charging stock for the system may be supplied through line 12 and valve 13 to pump 14 from which it is fed through line 15 and valve 16 into heating coil 17, which is located within a furnace 18 of any suitable form capable of heating the raw oil charging stock to the desired conversion temperature under the desired pressure.
  • the heated raw oil from heating coil 17 may be discharged through line '19 and valve 20 into line 6, commingling therein with the material from chamber 5, withdrawn through this line, and passing therewith to chamber 8, or the heated raw oil may be separately introduced into chamher 8 at any desired point by well known means, not, illustrated in the drawing.
  • vaporizing or flash distilling chamber 8 preferably employs a substantially reduced pressure relative to that utilized in reaction chamber 5 and the residual liquid conversion products from chamber 5 are subjected to further vaporization in this zone together with the heated raw oil from heating coil 1'7.
  • the process may be operated for the production of either residual liquid or a substantially non-fluid residual material such as petroleum coke or asphalt. Residual liquid or asphaltic material, when such is produced, may be withdrawn from chamber 8 through line 21 and valve 22 to cooling and storage or to any desired further treatment.
  • final light product of the system are also condensed within the fractionator and may be withdrawn as a side stream or streams of light reflux condensate through one or a piurality of lines 30 controlled by valves 31 and pass through line 32 to pump 33, by means of which they are fed through line 34 and valve 35 to heating coil 1 and comprise the only material supplied to this heating coil.
  • the lightest components of the vapors supplied to iraotionator 11, comprising materials within the boiling range of the desired final light product of the system and gas, are removed from the upper portion of the fractionator through line 36 and valve 37, are subjected to condensation and cooling in condenser 38 from which the resulting distillate and uneondensable gas passes through line 39 and valve 40 to be collected in receiver 41. Uncondensable gasmay be released from the receiver through line 42 and valve 43. Distillate may be withdrawn from the receiver through line 44 and valve 45.
  • Conversion temperatures employed within the heating coil to which the light reflux condensate is supplied may range from 900 to 1050 F. or thereabouts, preferably with superatmospheric pressure of from to 500 pounds, or more per square inch. Substantially this same range of pressures may be employed in the reaction chamber but the vaporizing or coking chamber as well as. thesucceeding fractionating, condensing and collecting portions of the system are preferably maintained at a substantially reduced pressure ranging from 100 pounds, or thereabouts, per square inch down to substantially atmospheric pressure.
  • the heating coil to which the raw oil charging stock is supplied may utilize conversion conditions either more or less severe than those to which the light reflux condensate is subjected, depending upon the nature of the charging stock.
  • a milder conversion temperature than that to which the light reflux is subjected ranging, for example, from 800 to 950 F.
  • a milder conversion temperature ranging, for example, from 800 to 950 F.
  • relatively light charging stock such as gas oil, l-zerosene distillate, pressure distillate bottoms, naphtha, straight-run gasoline, etc.
  • higher conversion temperatures ranging, for example, from 900 to 1100 R, my be employed the raw oil heating coil with pressures which may range from substantially atmospheric to 800 pounds, or more, per square inch.
  • the raw oil charging stock is an 18 A. P. I. gravity mid-continent fuel oil which is subjected to a temperature of about 890 F., at a pressure of approximately 200 pounds per square inch, and is then introduced into the flash distilling chamber.
  • Light reflux condensate from the fractionator of the system having an end boiling point of approximately 650 F., is independently subjected to a conversion temperature of approximately 925 F., at a superatmospheric pressure of about 350 pounds per square inch and is then introduced into the reaction chamber which is maintained at about the same pressure.
  • the vaporizing chamber is maintained at a pressure of approximately 50 pounds per square inch, which pressure is substantially equalized in the succeeding fraction-sting, condensing and collecting equipment. Heavy reflux condensate having an initial boiling point of about 650 F. is returned directly to the reaction chamber.
  • This operation may yield, per barrel of raw oil charging stock, about 55% of motor fuel having an anti-mock value equivalent to an octane number of approximately 78, about 38% of residual oil suitable for sale as fuel, the remainder being chargeable to uncondensable gas, loss and a negligible amount of coke.
  • a cracking process which comprises subjecting hydrocarbon oil to cracking conditions of temperature and pressure in an enlarged reaction zone, removing vapors and unvaporized oil from the reaction zone, flash distilling the unvaporized oil in a reduced pressure zone by pressure reduction, simultaneously heating charging I oil for the process to conversion temperature under pressure while flowing in a restricted stream through a heating zone and then discharging the same directly into the reduced pressure zone, removing vapors from the reduced pressure zone, iractionating the last-named vapors and the vapors removed from the reaction zone and separating' therefrom a relatively heavy reflux and a lighter reflux, introducing the heavy reflux direct- 1y to the reaction zone, heating the lighter reflux to cracldng temperature in a second heating zone and thence discharging the same into the reaction zone, and finally condensing theiraction ated vapors.
  • a cracking process which comprises subjecting hydrocarbon oil to cracking conditions of temperature and pressure in an enlarged reaction zone, removing vapors and unvaporized oil from the reaction zone, flash distilling the unvaporized oil in a reduced pressure zone by pressure reduction, simultaneously passing charging oil for the process through a heating zone and heating the same therein to cracking temperature under pressure, thence discharging the heated charging oil directly into the reduced pressure zone, subjecting the vapors evolved in the reduced pressure zone and those removed from the reaction zone to common fractionation and separating from the commingled vapors a relatively heavy reflux and a lighter reflux, introducing the heavy reflux directly to the reaction zone, heating the lighter reflux to higher cracking temperature than the charging oil and thence discharging the same into the reaction zone, and finally condensing the fractionated vapors.

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  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Description

Feb. 5, 1935. M. w. BARNES 1,989,731
r v CONVERSION OF HYDROCARBON OILS Filed May 27, 1952 VAPORIZING, FLASH DISTILLING OR COKNG CHAMBER FURNACE INVENTOR MARION W. BARNES W ZEW ATTORN 7' Patented Feb. 5, 1935 I 1,989,731
UNITEDSTATES PATENT OFFICE.
CONVERSION OF HYDROCARBON OILS Marion W. Barnes, Chicago, Ill., assignor to Universal Oil Products Company, Chicago, 111., a corporation of Delaware Application May 2'7, 1932, Serial No. 613,875
3 Claims. (Cl. 196-49) This invention relates to the conversion of hysystem are condensed and separated into a heavy dr'ocarbon oils and more particularly refers to an fraction, containing any coke-forming residual improved process and apparatus especially adaptmaterial carried over with the vapors from the ed to the conversion of relatively heavy oils to flash distilling operation, and lower boiling frac- 5 produce maximum yields of light distillate prodtions, subjecting said lower boiling fractions of 5 ucts, such as motor fuel of high anti-knock value, the reflux condensate to conversion temperature and a residual product of controlled quality. at superatmospheric pressure in a heating coil In cracking processes wherein the raw oil chargand communicating reaction chamber, returning ing stock is subjected to conversion in the same said heavy components of the reflux condensate heating coil with lighter insufllciently converted directly to the reaction chamber, subjecting re- 10 intermediate products of the operation milder sidual liquid from the reaction chamber to furconversion temperatures must be utilized when ther vaporization at reduced pressure, subjecting the charging stock is of relatively heavy nature, vapors from both the conversion and flash disthan the conversion temperature best suited for tilling operations to fractionation, as already del5 the treatment of the reflux condensate (interscribed, subjecting raw oil charging stock for the mediate conversion products), in order to prevent system to independently controlled conversion the excessive formation and deposition of coke conditions inaseparate heating coil and introducin the heating coil. Furthermore, in the type ing the heated material into the reduced pressure of process now in favor wherein the residual vaporizing chamber together with the residual products formed under high superatmospheric liquid conversion products from the reaction 20 pressure are subjected to flash distillation at rechamber. duced pressure for further vaporization and While the process of the present invention is wherein reflux condensate from the flashed vaparticularly adapted to the treatment of relapors is returned to the heating coil of the system tively heavy charging stock such as heavy crudes,
together with reflux condensate from the cracked residual oil, fuel oil and the like, it may also be 25 vapors, the combined reflux condensates often utilized to advantage for the treatment of lower contain small amounts of heavy residual material boiling oils and is not limited to any particular which have been carried over with the vapors type of charging stock. from the flash distilling chamber, which con- The attached diagrammatic drawing illustrates taminating material in the reflux is especially one specific form of apparatus incorporating the, 30 susceptible to coking under the conditions emfeatures of the present invention. These features ployed in the heating coil and often leaves a and the advantages will be more clearly underdeposit of carbon on the walls of the heating stood by reference to the following description of tubes, which necessitates short operating periods the drawing.
and prolonged clean-out time. Heating coil 1 is located within a furnace 2 of 35 By use of the novel features of the present inany suitable form and the oil supplied to this vention the above mentioned troubles are elimzone is heated to the desired conversion temperinated as neither the raw oil charging stock or ature preferably at substantial superatmospheric the heavy components of the reflux condensate pressure and is discharged through line 3 and pass through the high temperature heating coil valve 4 into reaction chamber 5 which is also 40 wherein the lighter reflux condensate is subjected preferably maintained at substantial superatmosto further conversion. This practice permits the pheric pressure. use of more severe conversion conditions, to which Final separation of vaporous and residual liquid said light reflux condensate is best suited, withconversion products may or may not be accomout encountering coking difliculties and yet also plished in chamber 5, as desired, and the heated 45 permits the desired degree of conversion for both oil from heating element 1 may be introduced in the raw oil charging stock and the heavy compothis zone at any desired point although the drawnents of the reflux condensate. ing shows only one point of introduction. Re-
In one of its speciflc embodiments the invention sidual liquid is withdrawn from the reaction '50 may comprise subjecting vapors resulting from chamber through line 6 and valve 7 to further 5 the conversion of hydrocarbon oil and subsequent vaporization in vaporizing or flash distilling flash distillation of the residual liquid conversion chamber 8 and vaporous conversion products may products to fractionation whereby the compoeither be withdrawn together with the residual nents of the vapors boiling above the end boiling liquid to chamber 8, in the manner described, or
point of the desired final light product of the may be separately removed from the reaction 55 chamber through line 9 and valve 10 and subjected to fractionation in fractionator 11.
Raw oil charging stock for the system may be supplied through line 12 and valve 13 to pump 14 from which it is fed through line 15 and valve 16 into heating coil 17, which is located within a furnace 18 of any suitable form capable of heating the raw oil charging stock to the desired conversion temperature under the desired pressure. The heated raw oil from heating coil 17 may be discharged through line '19 and valve 20 into line 6, commingling therein with the material from chamber 5, withdrawn through this line, and passing therewith to chamber 8, or the heated raw oil may be separately introduced into chamher 8 at any desired point by well known means, not, illustrated in the drawing.
vaporizing or flash distilling chamber 8 preferably employs a substantially reduced pressure relative to that utilized in reaction chamber 5 and the residual liquid conversion products from chamber 5 are subjected to further vaporization in this zone together with the heated raw oil from heating coil 1'7. The process may be operated for the production of either residual liquid or a substantially non-fluid residual material such as petroleum coke or asphalt. Residual liquid or asphaltic material, when such is produced, may be withdrawn from chamber 8 through line 21 and valve 22 to cooling and storage or to any desired further treatment. When the residual product of the process is reduced to coke in chamber 8 it may be allowed to accumulate in this zone to be removed therefrom when the operation of the chamber is discontinued and, when desired, a plurality of coking zones, similar to chamber 8 but not illustrated in the drawing, may be employed and may be operated either alternately or simultaneously to provide additional space for the accumulation of coke and thus prolong the operating cycle of the process. Vaporous products are wi ridrawn from chamber 8 through line 23 and valve 24 to line 9 and may pass thence to fractionation in fractionator 11 together with the vaporous products, if any, withdrawn from chamber 5 through line 9 and valve 10, as already described.
The vapors supplied to fractionator 11, comprising vaporous products resulting from both the conversion and flash distillation or coking operations, are separated by fractional condensation into three major fractions. The heaviest components of the vapors, including any residual material of cokeforming characteristics carried over with the vapors from chamber 8, collect, as heavy reflux condensate in the lower portion of the fractionator, are withdrawn therefrom through line 25 and valve 26 to pump 27 by means of which they are returned through line 23 and valve 29'to reaction chamber 5, entering this zone at any desired point, and being subjected therein to further conversion by direct contact with the heated materials from chamber 5. The intermediate components of the vapors, which boil above the boiling point of the desired. final light product of the system, are also condensed within the fractionator and may be withdrawn as a side stream or streams of light reflux condensate through one or a piurality of lines 30 controlled by valves 31 and pass through line 32 to pump 33, by means of which they are fed through line 34 and valve 35 to heating coil 1 and comprise the only material supplied to this heating coil. The lightest components of the vapors supplied to iraotionator 11, comprising materials within the boiling range of the desired final light product of the system and gas, are removed from the upper portion of the fractionator through line 36 and valve 37, are subjected to condensation and cooling in condenser 38 from which the resulting distillate and uneondensable gas passes through line 39 and valve 40 to be collected in receiver 41. Uncondensable gasmay be released from the receiver through line 42 and valve 43. Distillate may be withdrawn from the receiver through line 44 and valve 45.
Any of the usual operating expedients such as recirculating a portion of the distillate from the receiverof the system to the upper portion of the fractionator to assist cooling and fractionation in this zone and preheating a portion or all of the raw oil charging stock by heat recovered from within the system may be employed without departing from the scope of the invention although such well known features are not illustrated in the accompanying drawing.
Conversion temperatures employed within the heating coil to which the light reflux condensate is supplied may range from 900 to 1050 F. or thereabouts, preferably with superatmospheric pressure of from to 500 pounds, or more per square inch. Substantially this same range of pressures may be employed in the reaction chamber but the vaporizing or coking chamber as well as. thesucceeding fractionating, condensing and collecting portions of the system are preferably maintained at a substantially reduced pressure ranging from 100 pounds, or thereabouts, per square inch down to substantially atmospheric pressure. The heating coil to which the raw oil charging stock is supplied may utilize conversion conditions either more or less severe than those to which the light reflux condensate is subjected, depending upon the nature of the charging stock. With heavy charging stocks, such as crudes, residual oil, fuel oil and the lure, a milder conversion temperature than that to which the light reflux is subjected, ranging, for example, from 800 to 950 F., may be employed in the raw oil heating coil with pressures ranging from 100 to 500 pounds, or thereabouts, per square inch. When relatively light charging stock such as gas oil, l-zerosene distillate, pressure distillate bottoms, naphtha, straight-run gasoline, etc., are employed, higher conversion temperatures ranging, for example, from 900 to 1100 R, my be employed the raw oil heating coil with pressures which may range from substantially atmospheric to 800 pounds, or more, per square inch.
As a specific example of the operation of the process of the present invention, the raw oil charging stock is an 18 A. P. I. gravity mid-continent fuel oil which is subjected to a temperature of about 890 F., at a pressure of approximately 200 pounds per square inch, and is then introduced into the flash distilling chamber. Light reflux condensate from the fractionator of the system, having an end boiling point of approximately 650 F., is independently subjected to a conversion temperature of approximately 925 F., at a superatmospheric pressure of about 350 pounds per square inch and is then introduced into the reaction chamber which is maintained at about the same pressure. The vaporizing chamber is maintained at a pressure of approximately 50 pounds per square inch, which pressure is substantially equalized in the succeeding fraction-sting, condensing and collecting equipment. Heavy reflux condensate having an initial boiling point of about 650 F. is returned directly to the reaction chamber. This operation may yield, per barrel of raw oil charging stock, about 55% of motor fuel having an anti-mock value equivalent to an octane number of approximately 78, about 38% of residual oil suitable for sale as fuel, the remainder being chargeable to uncondensable gas, loss and a negligible amount of coke.
I claim as my invention:
1. A cracking process which comprises subjecting hydrocarbon oil to cracking conditions of temperature and pressure in an enlarged reaction zone, removing vapors and unvaporized oil from the reaction zone, flash distilling the unvaporized oil in a reduced pressure zone by pressure reduction, simultaneously heating charging I oil for the process to conversion temperature under pressure while flowing in a restricted stream through a heating zone and then discharging the same directly into the reduced pressure zone, removing vapors from the reduced pressure zone, iractionating the last-named vapors and the vapors removed from the reaction zone and separating' therefrom a relatively heavy reflux and a lighter reflux, introducing the heavy reflux direct- 1y to the reaction zone, heating the lighter reflux to cracldng temperature in a second heating zone and thence discharging the same into the reaction zone, and finally condensing theiraction ated vapors.
2. A cracking process which comprises subjecting hydrocarbon oil to cracking conditions of temperature and pressure in an enlarged reaction zone, removing vapors and unvaporized oil from the reaction zone, flash distilling the unvaporized oil in a reduced pressure zone by pressure reduction, simultaneously passing charging oil for the process through a heating zone and heating the same therein to cracking temperature under pressure, thence discharging the heated charging oil directly into the reduced pressure zone, subjecting the vapors evolved in the reduced pressure zone and those removed from the reaction zone to common fractionation and separating from the commingled vapors a relatively heavy reflux and a lighter reflux, introducing the heavy reflux directly to the reaction zone, heating the lighter reflux to higher cracking temperature than the charging oil and thence discharging the same into the reaction zone, and finally condensing the fractionated vapors.
3. The process as defined in claim 1 further characterized in that said char ing oil is of higher boiling point than said lighter reflux, the first-mentioned heating zone through which the charging oil is passed being maintained at lower temmrature than said second heating zone in which the lighter reflux is heated.
MARION W. BARNES.
US613875A 1932-05-27 1932-05-27 Conversion of hydrocarbon oils Expired - Lifetime US1989731A (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2463903A (en) * 1940-05-25 1949-03-08 Sinclair Refining Co Manufacture of gasoline

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2463903A (en) * 1940-05-25 1949-03-08 Sinclair Refining Co Manufacture of gasoline

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