US2284493A - Combination cracking operation - Google Patents

Combination cracking operation Download PDF

Info

Publication number
US2284493A
US2284493A US294110A US29411039A US2284493A US 2284493 A US2284493 A US 2284493A US 294110 A US294110 A US 294110A US 29411039 A US29411039 A US 29411039A US 2284493 A US2284493 A US 2284493A
Authority
US
United States
Prior art keywords
line
tower
exchangers
oil
temperature
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
US294110A
Inventor
Henry D Noll
Otls L Branson
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.)
ExxonMobil Oil Corp
Original Assignee
Socony Vacuum Oil Co 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 Socony Vacuum Oil Co Inc filed Critical Socony Vacuum Oil Co Inc
Priority to US294110A priority Critical patent/US2284493A/en
Application granted granted Critical
Publication of US2284493A publication Critical patent/US2284493A/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
    • C10G51/00Treatment of hydrocarbon oils, in the absence of hydrogen, by two or more cracking processes only
    • 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
    • C10G51/00Treatment of hydrocarbon oils, in the absence of hydrogen, by two or more cracking processes only
    • C10G51/06Treatment of hydrocarbon oils, in the absence of hydrogen, by two or more cracking processes only plural parallel stages only

Definitions

  • a reduced crude heated by exchange is fed into an evaporator tower which receives all of the hot streams of the system.
  • An overhead from the evaporator tower passes to a bubble tower.
  • the residue from the bottom of the evaporator tower passes to a fuel flash tower.
  • a heavy gas oil fraction withdrawn from near the top of the evaporator tower and a light gas oil withdrawn from the bottom of the bubble tower are passed through separate coils of a cracking furnace and then passed together through'external transfer line heat exchangers. From the transfer line exchangers the cracked gas oils are passed into thebottom of the evaporator tower.
  • a heavy naphtha fraction heated by exchange with the cracked gas oils in the transfer line exchangers is passed into a reforming furnace. From the reforming furnace the reformed naphtha passes through additional external transfer line heat exchangers and then is passed into the bottom of the evaporator tower.
  • a reduced crude fraction is withdrawn from near the middle of the evaporator tower and passed through the transfer line exchangers of the reformer furnace in indirect heat exchange with the reformed heavy naphtha passing therethrough and then injected into the reformed heavy naphtha line going into the exchangers and thereby iiowed through the transfer line exchangerswith the reformed heavy naphtha and then into the bottom of the evaporator tower.
  • Overhead distillate from bubble tower 4 passes through line I9 containing exchanger 2 and cooler Illa to a separator II.
  • Uncondensed gas from chamber II passes tofuel and liquid is sent principally through line I2 to a stabilizing unit (not shown) with a portion being returned through line I3 to the top of tower 4 as reflux.
  • Light gas f oil withdrawn from the bottom of bubble tower 4 is sent through line I8 to the other set of coils lin cracker I'I.
  • the cracked heavy and light gas oil withdrawn from cracker I1 are fed together through line I9 into the external transfer line exchangers 20. and from exchangers 29, the gas oils pass through line 2
  • the heavy naphtha passes from exchangers 20 to the coils of the reformer furnace 23 and is subjected reforming therein.
  • the heavy naphtha withdrawn from reformer 23 through line 24 is fed into transfer line exchangers 25. and from exchangers 25, the heavy naphtha passes through line 26 into the bottom of tower 5.
  • a reduced crude fraction withdrawn from near the middle of tower 5 is passed by line 21, containing gas separator 28 from which vapors are passed back to tower 5 through line 29, to transfer line exchangers 25.
  • VThe reduced crude fraction is passed through exchangers 25 and heated up to approximately viscosity breaking temperature therein by indirect heat exchange and the thus heated reduced crude fraction is then injected into the reformed heavy naphtha line 24 leaving reformer furnace 23 and fed along with the reformed heavy naphtha back through exchangers 25 and viscosity broken therein and then passed along with the reformed heavy rsiaphtha through line 26 into the bottom of tower
  • An important feature of the present invention is the dual function of the transfer line exchangers of the reformer furnace, i.
  • the construction and operation of the reformer transfer line exchangers must be such as to aiiord proper contacting time of the oils passing therethrough at the required temperatures for viscosity breaking of the reduced crude.
  • temperatures and contact times may vary inversely over an appreciable range and may be somewhat diiferent depending on the particular oils and fractions being treated and the amount of viscosity breaking desired, it would be diicult to specify any denite values for these conditions which would suit all operations. However, as such conditions as these are often encountered by workers in the art, it is believed little trouble will be had in adapting the present invention to any particular operation.
  • Sample calculation Soaking time can be calculated from the average volume of the oil vapors in the soaking zone and the volume of the soaking zone.
  • the volume of the soaking zone is calculated from the cold volume of oil feed in barrels per day and the soaking factor.
  • the soaking factor is dened as .Kr/Kaum r. (coil vol. in cu. ft./bbl./day).
  • Kir/Kano is the ratio of the cracking reaction velocity constant at a temperature T to the value at 800 F.
  • the soaking factor is evaluated by graphical integration of a plot of Kr/Kauo vs cu. ft. /bbL/day.
  • the average temperaturev is about 890% F. and the pressure about 600 lbs./sq. in. absolute in the soaking zone.
  • the critical temperature and pressure of the gas will be about 104 F. and 691 iba/sq. in.
  • the deviation factor is 0.993.
  • the number of mols per minute is Gas. Assume same number of mois formed as of gasoline.
  • transfer line exchangers of the reformer furnace have been described and shown as' the viscosity-breaking unit, it is to be understood that other transfer line exchangers for an oil of suiiiciently high temperature might be used such as the transfer line exchangers 20 of the light and heavy gas oil cracker I1.
  • transfer line exchangers of one oil line might be used to preheat the reduced crude fraction and the transfer line exchangers of another oil line used to viscosity break the fraction.
  • the reduced crude fraction in the preferred embodiment shown might be preheated in exchangers 20 of cracker I1 and viscosity broken in exchangers 25 of reformer 23. It is to be understood further that the present invention is not restricted to the exact cracking and reforming systern herein shown but, as is obvious, may be applied to such systems in general.
  • the temperature to which the reduced crude fraction should be preheated before being injected into the reformed naphtha should be suiiiciently high that when combined with reformed heavy naphtha the mixture will have an eicient viscosity breaking temperature.
  • This preheated temperature of the reduced crude fraction will depend therefore on the temperature of the reformed naphtha or other stock and the relative proportions of the oils being mixed.
  • the reduced crude fraction usually should be preheated to substantially the viscosity breaking temperature before being injected into the reformed heavy naphtha. It will be noted that by the present invention wherein the reduced crude fraction is preheated and viscosity broken in an external unred zone, the fraction is never subjected to the conditions of directly fired tubes with the attendant danger of coke deposition.
  • Reduced crude from a mid-continent stock is fed at the rate of 6000 bbl/day through line I containing exchangers 2, and 3 into evaporator -tower 5.
  • Tower 5 is -maintained under 250 lbs/sq. in, pressure andv has a temperature of 720" F. at the top' and 800 F. at the lbottom. Vapor from the top of tower 5 passes through line 6 containing exchanger 3 into bubble tower 4.
  • Bubble tower 4 is maintained'under a pressure of 240 lbs/sq. in. and has a top temperature of 420 F. and a bottom temperature of 600 F.
  • Residue from tower 5 passes through line l to fuel ash tower'8. the flash distillate from which is returned to the top of tower 5 and the residue'yields 2730 bbls./day of fuel oil.
  • Overhead vapor from bubble tower 4- passes througnline I0 containing exchanger 2 and cooler Illa to vapor separator II which is maintained under a pressure of 225#/sq. in. and at a temperature of F.
  • the gaseous product removed from the top of separator I I goes to fuel, while the residue is'withdrawn at the bottom, a portion of which is returned through line I3 as a reflux to the top of bubble tower 4, and the re- .;.mainder of which is sent through line I2 to a stabilizing unit (not shown).
  • Light gas oil recycle withdrawn through line I8 at the ,bottom of bubble tower 4 is passed at the rate of 10,000 bbls./day to one set of coils in cracker I1.
  • Heavy gas oil withdrawn through line I4 from near the top of tower 5 ⁇ passes into vvapor separator I5 maintained at set of coils in cracker I1.
  • the cracked light gas oil at a temperature of 980 F. and the cracked heavy gas oil at a temperature of 925 F. are combined in line I6 and fed together under a pressure of '150#/sq. in. into exchangers 20 and then through line 2l into the bottom of tower 5.
  • the cracked gas oils remain in exchangers 20 for about 42 seconds, in which it is subjected to soaking for about 21 seconds since only about one-half of the exchanger volume is above 800 F.
  • Heavy naptha at the rate of about 700 bbls./ day is fed through line 22 containing exchanger 20, wherein it is heated up by exchange with the cracked gas oil, to reformer furnace 23, the reformed heavy naptha leaves the reformer furnace at a temperature of around 1000 F. through line 24 where it is mixed with a reduced crude fraction and the mixture fed-into exchangers 25 at a temperature of about 936 F.
  • the mixture remains in exchangers 25 for about 7 seconds during which time viscosity breaking of the reduced crude fraction admixed therewith occurs.
  • the mixture leaves exchanger 25 at a temperature of about 850 F. and is passed through line 26 into the bottom of tower 5.
  • the reduced crude fraction which is to be combined with the reformed heavy naphtha is withdrawn from near the middle of tower 5 through line 21 and passed into vapor separator 2B which is maintained at '750 F. Vapors fromseparator 28 are returned to tower 5 through line 29.
  • the liquid from separator 28 passes through line 21 at the rate of 800 bbls./day to exchangers 25 and passes through exchangers 25 wherein it is heated up by exchange and then injected into an overhead vapor from said tower is passed to a bubble tower, light gas oil from said bubble tower and heavy gas oil from said evaporator tower are sent through separate heated coils under selective cracking conditions therefor and the cracked oils therefrom are passed to said evaporator tower, and wherein preheated naphtha is passed through a heated reforming coil under reforming conditions to effect substantial reforming thereof, the improvement which cornprises passing a reduced crude withdrawn from said evaporator tower through an external suitred soaking zone to preheat same to a predetermined temperature, introducing such preheated reduced crude into substantially reformed naphtha withdrawn from said heated reforming coil and regulating the predetermined temperature and amount of the preheated reduced crude so introduced that the resultant temperature of the mixture is at an emcient viscosity-breaking temperature for the reduced crude.

Description

May 26, 1942. H. D. NoLL ETAL COMBINATION GRACKING OPERATION Filed Sept. 9, 1939 u w 5 s RLN Y OLA TOR yN NN R E.8 O WOL. n Rw. .mw H Y Patented May 26, 1942 UNITED sTATEs PATENT ,OFFICE 2,284,493 l CQMBINATION CRACKING OPERATION Henry D. Noll, Wenonah, N. J., and Otis L. Branson, Beaumont,
Vacuum Oil Company,
Tex., assignors to Socony- Incorporated. New York,
N. Y., a corporation of New York I Application september 9, 1939, serai No. 294,110
(ci. '19e-5s) 1 Claim.
vaffords more eiiicient heat utilization.
In operating a conversion system in accordance with a preferred embodiment of our invention, a reduced crude heated by exchange is fed into an evaporator tower which receives all of the hot streams of the system. An overhead from the evaporator tower passes to a bubble tower. The residue from the bottom of the evaporator towerpasses to a fuel flash tower. A heavy gas oil fraction withdrawn from near the top of the evaporator tower and a light gas oil withdrawn from the bottom of the bubble tower are passed through separate coils of a cracking furnace and then passed together through'external transfer line heat exchangers. From the transfer line exchangers the cracked gas oils are passed into thebottom of the evaporator tower. A heavy naphtha fraction heated by exchange with the cracked gas oils in the transfer line exchangers is passed into a reforming furnace. From the reforming furnace the reformed naphtha passes through additional external transfer line heat exchangers and then is passed into the bottom of the evaporator tower.
A reduced crude fraction is withdrawn from near the middle of the evaporator tower and passed through the transfer line exchangers of the reformer furnace in indirect heat exchange with the reformed heavy naphtha passing therethrough and then injected into the reformed heavy naphtha line going into the exchangers and thereby iiowed through the transfer line exchangerswith the reformed heavy naphtha and then into the bottom of the evaporator tower.
For a more complete understanding of the present invention reference will be had to the accompanying drawing wherein the figure is a diagrammatic drawing of a preferred conversion system employing our invention. y
In the drawing reduced crude is fed through line I, containing exchangers 2 and 3 of the bubble tower 4 and evaporator tower 5, respectively, intovthe middle of evaporator tower 5. Overhead distillate from the evaporator tower line 6 through exchanger Sinto bubble towe 4. Residue from the evaporator tower is passed through line 'I to fuel flash tower 9, the ash distillate from which is returned to the top of evaporator tower 5 through line 9.
Overhead distillate from bubble tower 4 passes through line I9 containing exchanger 2 and cooler Illa to a separator II. Uncondensed gas from chamber II passes tofuel and liquid is sent principally through line I2 to a stabilizing unit (not shown) with a portion being returned through line I3 to the top of tower 4 as reflux.
A heavy gas oil fraction withdrawn from tower 5 through line I4, containing vapor separator I5 from which vapors are returned to tower 5 through line I6, is sent to one set of coils in the light and heavy gas oil cracker I1. Light gas f oil withdrawn from the bottom of bubble tower 4 is sent through line I8 to the other set of coils lin cracker I'I. The cracked heavy and light gas oil withdrawn from cracker I1 are fed together through line I9 into the external transfer line exchangers 20. and from exchangers 29, the gas oils pass through line 2| to the bottom of tower .transfer line exchangers 20 wherein it is heated up by indirect heat exchange with the cracked light and heavy gas oil passing therethrough. The heavy naphtha passes from exchangers 20 to the coils of the reformer furnace 23 and is subjected reforming therein. The heavy naphtha withdrawn from reformer 23 through line 24 is fed into transfer line exchangers 25. and from exchangers 25, the heavy naphtha passes through line 26 into the bottom of tower 5.
A reduced crude fraction withdrawn from near the middle of tower 5 is passed by line 21, containing gas separator 28 from which vapors are passed back to tower 5 through line 29, to transfer line exchangers 25. VThe reduced crude fraction is passed through exchangers 25 and heated up to approximately viscosity breaking temperature therein by indirect heat exchange and the thus heated reduced crude fraction is then injected into the reformed heavy naphtha line 24 leaving reformer furnace 23 and fed along with the reformed heavy naphtha back through exchangers 25 and viscosity broken therein and then passed along with the reformed heavy rsiaphtha through line 26 into the bottom of tower An important feature of the present invention is the dual function of the transfer line exchangers of the reformer furnace, i. e., the function of serving as an external unflred heating chamber for heating the reduced crude fraction up to approximately viscosity-breaking temperatures andthe further function of se1 ving as an external unfired viscosity-breaking unit'for the reduced crude fraction. |Thus, as seen above. these exchangers heat the reduced crude fraction up to temperature by heat exchange and then viscosity breaks the heated reduced crude as it is fed back through the exchangers in admixture with reformed heavy naphtha. It is obvious, of course, that use may be made of this important feature of our invention in conversion systems other than the preferred embodiment described herein.
The construction and operation of the reformer transfer line exchangers must be such as to aiiord proper contacting time of the oils passing therethrough at the required temperatures for viscosity breaking of the reduced crude.
Ii it is required to control the volume of injected oil over wide ranges, this may be accomplished by introduction of reflux from line 9 into tower at points A and B. The introduction at A will aifectthe gravity of the fuel eliminated and tend to produce a lighter cycle in the in- Jection flow stock passing through line 21 to exchangers 25. With increased reflux at B, the
rate of injection iiow will increase, whereas a decrease of reflux produces less injection ow material.
Since the temperatures and contact times may vary inversely over an appreciable range and may be somewhat diiferent depending on the particular oils and fractions being treated and the amount of viscosity breaking desired, it would be diicult to specify any denite values for these conditions which would suit all operations. However, as such conditions as these are often encountered by workers in the art, it is believed little trouble will be had in adapting the present invention to any particular operation.
On the other hand, if precise determination of soaking time is desired, it may be made as shown in the following sample calculation for determining proper soaking time in exchangers 25 to give a 10% crack per pass on black oil under certain given conditions.
Sample calculation Soaking time can be calculated from the average volume of the oil vapors in the soaking zone and the volume of the soaking zone. The volume of the soaking zone is calculated from the cold volume of oil feed in barrels per day and the soaking factor.
The soaking factor is dened as .Kr/Kaum r. (coil vol. in cu. ft./bbl./day). Kir/Kano is the ratio of the cracking reaction velocity constant at a temperature T to the value at 800 F. In general, the soaking factor is evaluated by graphical integration of a plot of Kr/Kauo vs cu. ft. /bbL/day.
Soaking volume-Given that the oil vapors enter exchanger or soaking zone at 936 F. and leave at 850. By assuming the temperature falls logarithmically intermediate temperatures can be found and, hence, K T/Kaoo. In the following table the first column gives the fraction of the total exchanger volume, the second column the corresponding temperatures, the third column the value of Kr/Kaoo, and in the fourth column the integration by Simpsons rule. The total feed to the soaking zone is 7000 B/D of heavy naphtha and 8000 B/D of black oil, a total of 15000 B/D.
Using V for exchanger volume and h for Width of strip in Simpsons rule Fraction of Integration exchanger Tgllgr' K r/ Km h o 25X vo umo 15000 F. 0. 00 936 39. 0 39. 0 0. 25 914 22. 7 90. 8 0. 50 893 13. 3 26. 6 0. 873 7. 5' 30. 0 1 o0 85o l. 2 4. 2
Then by Simpsons rule for integration the soaking factor is- }X190.6X0.25X V-=0.00106V From data for Magnolia operation, it is known that the soaking factor should be numerically equal-to 0.065 to give a 10% C/P on the black oil. Hencee 0.065,=0.00106 V and V=61.4 cu. ft.
Oil vapor volume-Because of the extreme conditions imposed on the oil vapor, its volume cannot be calculated from the ideal gas law without using a deviation factor. The average temperaturev is about 890% F. and the pressure about 600 lbs./sq. in. absolute in the soaking zone.
Black oil for injection- Given that the A. S. T;TM.-50% point is 850 F., the API gravity is 20 and the U. 0. P. characterization factor is 11.5, it can be determined that the average molecular weight is 370 and that the critical temperature and pressure are 1160 F. and 175 lbs./sq. in. respectively. The deviation factor is then determined to be 0.517.
Reformed gasolina- Given the gravity as 58.3 API and the temperature at which 10, 30, 50, 70, and is evaporated in the A. S. T. M. distillation as being 157, 223, 275, 323, 375 F. respectively. 'Ihese data determine the U. O. P. characterization factor as being 12.0, the molecular weight at 116.5, and the critical temperature and pressure to be 595 F. and 398 lbs./sq. in. The deviation factor is then 0.755.
Gas.-By assuming a molecular weight of 33, the critical temperature and pressure of the gas will be about 104 F. and 691 iba/sq. in. The deviation factor is 0.993.
Mols and liquid volumes of materials.-Black oil.
At the average condition about 5% converted to gasoline, hence 8000 0.95=7600 B/D of black oil (20 API equivalent to 7.778 iba/gal.)
'Ihe number of mois per minute is Gasoline.
The number of mols per minute is Gas. Assume same number of mois formed as of gasoline.
Vapor volumes.-The corrected gas law is cu. lft. 1bs./sq. in. R' s 1071 deg. Rankine Black oil- 24.12X 4.65X0.517= l58.0 cu. ft. Gasoline 24.12X11.5QXO.755l-209.3 cu. ft. Gas 24.1 2X11.50X0.993=2'15.2 cu. ft.
Total volume 542.5 cu. ft. Soaking time=61f4i =0.1l3 minutes--or 6.8 sec.
-problems and by adjustments arrive at satisfactory operating conditions, as is often done in cracking practice.
While the transfer line exchangers of the reformer furnace have been described and shown as' the viscosity-breaking unit, it is to be understood that other transfer line exchangers for an oil of suiiiciently high temperature might be used such as the transfer line exchangers 20 of the light and heavy gas oil cracker I1. Likewise the transfer line exchangers of one oil line might be used to preheat the reduced crude fraction and the transfer line exchangers of another oil line used to viscosity break the fraction. Thus the reduced crude fraction in the preferred embodiment shown might be preheated in exchangers 20 of cracker I1 and viscosity broken in exchangers 25 of reformer 23. It is to be understood further that the present invention is not restricted to the exact cracking and reforming systern herein shown but, as is obvious, may be applied to such systems in general.
The temperature to which the reduced crude fraction should be preheated before being injected into the reformed naphtha should be suiiiciently high that when combined with reformed heavy naphtha the mixture will have an eicient viscosity breaking temperature. This preheated temperature of the reduced crude fraction will depend therefore on the temperature of the reformed naphtha or other stock and the relative proportions of the oils being mixed. As a matter of practice it will be found that the reduced crude fraction usually should be preheated to substantially the viscosity breaking temperature before being injected into the reformed heavy naphtha. It will be noted that by the present invention wherein the reduced crude fraction is preheated and viscosity broken in an external unred zone, the fraction is never subjected to the conditions of directly fired tubes with the attendant danger of coke deposition.
In order to furtherillustrate'the present in;-
vention we will describe a specific operation using a mid-continent reduced crude, however, it is to be understood the invention is not to be limited by this example as there may be variations therefrom without departing from the scope of the invention.
Reduced crude from a mid-continent stock is fed at the rate of 6000 bbl/day through line I containing exchangers 2, and 3 into evaporator -tower 5. Tower 5 is -maintained under 250 lbs/sq. in, pressure andv has a temperature of 720" F. at the top' and 800 F. at the lbottom. Vapor from the top of tower 5 passes through line 6 containing exchanger 3 into bubble tower 4. Bubble tower 4 is maintained'under a pressure of 240 lbs/sq. in. and has a top temperature of 420 F. and a bottom temperature of 600 F. Residue from tower 5 passes through line l to fuel ash tower'8. the flash distillate from which is returned to the top of tower 5 and the residue'yields 2730 bbls./day of fuel oil.
Overhead vapor from bubble tower 4- passes througnline I0 containing exchanger 2 and cooler Illa to vapor separator II which is maintained under a pressure of 225#/sq. in. and at a temperature of F. The gaseous product removed from the top of separator I I goes to fuel, while the residue is'withdrawn at the bottom, a portion of which is returned through line I3 as a reflux to the top of bubble tower 4, and the re- .;.mainder of which is sent through line I2 to a stabilizing unit (not shown).
Light gas oil recycle withdrawn through line I8 at the ,bottom of bubble tower 4 is passed at the rate of 10,000 bbls./day to one set of coils in cracker I1. Heavy gas oil withdrawn through line I4 from near the top of tower 5 `passes into vvapor separator I5 maintained at set of coils in cracker I1. The cracked light gas oil at a temperature of 980 F. and the cracked heavy gas oil at a temperature of 925 F. are combined in line I6 and fed together under a pressure of '150#/sq. in. into exchangers 20 and then through line 2l into the bottom of tower 5. The cracked gas oils remain in exchangers 20 for about 42 seconds, in which it is subjected to soaking for about 21 seconds since only about one-half of the exchanger volume is above 800 F.
Heavy naptha at the rate of about 700 bbls./ day is fed through line 22 containing exchanger 20, wherein it is heated up by exchange with the cracked gas oil, to reformer furnace 23, the reformed heavy naptha leaves the reformer furnace at a temperature of around 1000 F. through line 24 where it is mixed with a reduced crude fraction and the mixture fed-into exchangers 25 at a temperature of about 936 F. The mixture remains in exchangers 25 for about 7 seconds during which time viscosity breaking of the reduced crude fraction admixed therewith occurs. The mixture leaves exchanger 25 at a temperature of about 850 F. and is passed through line 26 into the bottom of tower 5.
The reduced crude fraction which is to be combined with the reformed heavy naphtha is withdrawn from near the middle of tower 5 through line 21 and passed into vapor separator 2B which is maintained at '750 F. Vapors fromseparator 28 are returned to tower 5 through line 29. The liquid from separator 28 passes through line 21 at the rate of 800 bbls./day to exchangers 25 and passes through exchangers 25 wherein it is heated up by exchange and then injected into an overhead vapor from said tower is passed to a bubble tower, light gas oil from said bubble tower and heavy gas oil from said evaporator tower are sent through separate heated coils under selective cracking conditions therefor and the cracked oils therefrom are passed to said evaporator tower, and wherein preheated naphtha is passed through a heated reforming coil under reforming conditions to effect substantial reforming thereof, the improvement which cornprises passing a reduced crude withdrawn from said evaporator tower through an external uniired soaking zone to preheat same to a predetermined temperature, introducing such preheated reduced crude into substantially reformed naphtha withdrawn from said heated reforming coil and regulating the predetermined temperature and amount of the preheated reduced crude so introduced that the resultant temperature of the mixture is at an emcient viscosity-breaking temperature for the reduced crude. passing the mixture through said unred soaking zone under viscosity-breaking conditions, in indirect heat exchange with said reduced-crude passing therethrough alone, to eifect a substantial viscositybreaking of the reduced crude which is mixed with said naphtha, and then passing the mixture from said soaking zone to said evaporator tower for separation into vaporous and liquid products.
HENRY D. NOLL. OTIS L. BRANBON.
GERTIFIGATE oF conmzcuou. Pnentno. 2,231hh95. y nay 26, 19m. HENRY n. Nom., nu..
I't 1a herebycerttied that error appear; 1n the printed specification 'of the above nu'mbered. p atent requiringcorrecton as follows: Page 1, aecond column,A line 50, after "subjected" insert --to--g page 2I second c olumn, line 51 for *890%* read .890f; page 5, second column, line 57, for *line 16" read --line 19"; line 1lb., fo;` 'F700' read 7O00; line 66, for *80o* read -'8oo; and that the said Letters Patent should be read with this correction therein that the seme may conform to the record of the case 1h the Patent office.
Signed end sealedlths 29th day of September, A. D. 1%2.
Henry Van Aredale,
(Seal) Acting Commissioner of Patents.
US294110A 1939-09-09 1939-09-09 Combination cracking operation Expired - Lifetime US2284493A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US294110A US2284493A (en) 1939-09-09 1939-09-09 Combination cracking operation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US294110A US2284493A (en) 1939-09-09 1939-09-09 Combination cracking operation

Publications (1)

Publication Number Publication Date
US2284493A true US2284493A (en) 1942-05-26

Family

ID=23131925

Family Applications (1)

Application Number Title Priority Date Filing Date
US294110A Expired - Lifetime US2284493A (en) 1939-09-09 1939-09-09 Combination cracking operation

Country Status (1)

Country Link
US (1) US2284493A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2529790A (en) * 1947-12-30 1950-11-14 Phillips Petroleum Co Thermal and catalytic cracking of hydrocarbons
US4097544A (en) * 1977-04-25 1978-06-27 Standard Oil Company System for steam-cracking hydrocarbons and transfer-line exchanger therefor
US4190520A (en) * 1978-01-03 1980-02-26 Uop Inc. Hydrocarbon conversion process
US4343958A (en) * 1978-01-03 1982-08-10 Uop Inc. Hydrocarbon isomerization process

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2529790A (en) * 1947-12-30 1950-11-14 Phillips Petroleum Co Thermal and catalytic cracking of hydrocarbons
US4097544A (en) * 1977-04-25 1978-06-27 Standard Oil Company System for steam-cracking hydrocarbons and transfer-line exchanger therefor
US4190520A (en) * 1978-01-03 1980-02-26 Uop Inc. Hydrocarbon conversion process
US4343958A (en) * 1978-01-03 1982-08-10 Uop Inc. Hydrocarbon isomerization process

Similar Documents

Publication Publication Date Title
US2284493A (en) Combination cracking operation
US2149860A (en) Conversion of hydrocarbon oils
US2358912A (en) Conversion of hydrocarbons
US2247740A (en) Conversion of hydrocarbon oils
US2072524A (en) Process for converting hydrocarbon oils
US2283851A (en) Hydrocarbon conversion process
US2055015A (en) Conversion of hydrocarbon oil
US2339917A (en) Hydrocarbon conversion process
US2272285A (en) Conversion of hydrocarbon oils
US2100849A (en) Conversion of hydrocarbon oils
US1933507A (en) Cracking in homogeneous state
US2069392A (en) Cracking of hydrocarbon oils
US2066808A (en) Art of converting hydrocarbon oil
US2144826A (en) Conversion of hydrocarbon oils
US2210265A (en) Conversion of hydrocarbon oils
US2128898A (en) Conversion of hydrocarbon oils
US1960909A (en) Art of cracking hydrocarbons
US2338794A (en) Conversion of hydrocarbon oils
US2348867A (en) Combination cracking process
US2356019A (en) Conversion of hydrocarbon oils
US2081342A (en) Conversion of hydrocarbon oils
US2126988A (en) Conversion of hydrocarbon oils
US1957810A (en) Hydrocarbon oil conversion
US2000399A (en) Hydrocarbon oil conversion
US2105554A (en) Treatment of hydrocarbon oils