US2221702A - Fractionation of hydrocarbon vapor mixtures - Google Patents
Fractionation of hydrocarbon vapor mixtures Download PDFInfo
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- US2221702A US2221702A US238020A US23802038A US2221702A US 2221702 A US2221702 A US 2221702A US 238020 A US238020 A US 238020A US 23802038 A US23802038 A US 23802038A US 2221702 A US2221702 A US 2221702A
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING 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
- C10G7/00—Distillation of hydrocarbon oils
- C10G7/02—Stabilising gasoline by removing gases by fractioning
Definitions
- the upper column serves primarily as a condenser and dephlegmator wherein the vapors are contacted with cool reflux condensate.
- This reflux medium is obtained by withdrawing unstabilized gasoline condensate from the intermediate portion of the tower, cooling it and recirculating it tothe upper portion of the condensing column.
- Exl 0 cess unstabilized condensate drawn from the base of the condensing'column is delivered to the lower or stabilizing column, and heat is supplied to the base of the stabilizing, column, usually through the medium of a boiler of more or less l e. conventional type.
- the condensate from the upper or condensing column is rectified and stabilized, the vapors liberated during stabilization being returned to the upper or condensing column.
- This may be either a small coil located in the head of the column, or it may comprise a separate condenser receiving vapors from the top of the column, together with means for recirculating condensate thereby obtained into the head of the column.
- a temperature differential must be maintained throughout the column and this means that the 45 temperatures of the outlet vapors will be low, not far removed from atmospheric. This in turn means that temperature differential between the vapors leaving the top of the column and the recycled reflux is'low; and it is difiicult to supply adequate cooling on account of this low ter'nperature difierential.
- the stabilized condensate which is to be returned as reflux is withdrawn from an inter+ mediate portion of the column at a temperature substantially higher than that maintained in the upper portion of the column, so that there is a very large temperature differential between the temperature of the side stream as withdrawn from the column and the temperature of the same material when returned as reflux; this vastly increases the ease and economy of operation.
- the Ostergaard system also has the advantage that the cooling is applied to a liquid stream rather than to a vapor stream and is somewhat more efficient on that account.
- the vapors at the point of re-entry should contain considerably less of the higher boiling constituents present than the vapors and liquid at the point of withdrawal. Consequently, the reflux material in the Ostergaard system inevitably contains a slightly higher proportion of high boiling, i. e. gasoline, constituents thanis desirable for utmost fractionatingefiiciency.
- mixed hydrocarbon vapors of the character referred to hereinabove such as vapors produced in the cracking of hydrocarbon oils from which constituents heavier than gasoline have been removed, are introduced into a condenser-stabilizer column differing from the Ostergaard column in that three instead of two sections are provided.
- the two lower sections are substantially identical in construction and operation to the two sections of the Ostergaard condenser- I-Iowever, I also provide a third section superimposed upon the intermediate or condensing section and provided with means for condensing or dephlegmating the vapors reaching the top of this third section to produce a condensate which is then returned to the head of the third section as a cooling and reflux medium therefor.
- the bulk of the cooling is. supplied by withdrawing a side stream and returning it to the tem. Additional cooling and rectification is,
- the primary purpose being to correct any lack of proper equilibrium at the top of the intermediate section and thereby to insure that all normallyliquid constituents desired to be included in the stabilized gasoline fraction are condensed and held within the column and do not pass out in uncondensed form.
- This system is of especial advantage in all instances where the character of the vapors is such that use of the Ostergaard system tends to leave a small amount of gasoline constituents uncondensed in the overhead product from the column.
- the single figure is a more or less'diagrammatical and conventionalized elevational viewof a condensing and stabilizing column, adaptedfor the performance of the process of my invention.
- a mixture of hydro carbon vapors containing gasolinev constituents and lighter normally gaseous constituents are shown entering the system through a line I.
- these vapors constitute the overhead product from the main fractionator (not shown) of an oil cracking or gas polymerization unit, being free or substantially free from constituents boiling above the normal gasoline boiling-point range and containing, in addition to hydrocarbons having boiling points within the gasoline boiling-point range, considerable quantities of lower boiling constituents, such as hydrocarbons having not more than four carbon atoms per molecule.
- vapors are first introduced into an indirect heat exchanger or cooler 2 wherein their temperature is substantially reduced.
- the partly cooled vapor is then passed through a line 3 into the lower part of a fractionating column 4 which, as shown, comprises the mid-section of a fractionating column also having upper and lower sections 5 and 6, respectively.
- a fractionating column 4 which, as shown, comprises the mid-section of a fractionating column also having upper and lower sections 5 and 6, respectively.
- Each of the sections 4, 5 and 6 is internally provided with a weir device 8 is provided between the mid-sec- A tion 4 and the lower or stabilizing section 6.
- suitable weir device as illustrated in the drawing, is provided with a vapor conduit 9 and a liquid downflow pipe ll].
- Relatively cool reflux oil obtained as set forth hereinbelow, is introduced into the upper portion of the mid-section 4 through a line 12.
- a portion of the condensate thus obtained is withdrawn from the weir device 8 through a line l3 having, a valve l4 and is delivered through a line l5 to an indirect cooler l6.
- the cooled condensate leaving the cooler I6 passes through a line I! to a pump l8 which in turn delivers it to the line [2 into the upper portion of the midsection 4.
- reflux for the midsection 4 may be provided by withdrawing faportion of the internal reflux from a trap tray or weir device 19 located above the point of introduction of the vapors into the mid-section 4.
- Reflux condensate thus withdrawn passes through a line 20 having a valve 2
- Unstabilized condensate collecting in the weir device 8 and not withdrawn through the pipe l3 passes through the downflow pipe l6 into the lower or stabilizing section 6 of the column, the base of which is in communication through a valved liquid line 23 and a vapor-return line 24 with a re-boiler 25 of conventional design.
- the re-boiler 25 is provided with an internal coil 26 or other means for supplying heat thereto.
- Stabilized gasoline is withdrawn from the bottom of the re-boiler 25 through an outlet line 21 having a valve 28.
- the unstabilized condensate is rectified and stabilized to remove constituents too light to be included in the final gasoline product. These constituents, in vapor form, re-enter the mid-section 4 through the vapor line 9.
- a method of condensing stabilized gasoline from vapors comprising a mixture of hydrocarbons having boiling points within a gasoline boiling-point range and hydrocarbons having lower boiling points, such as are produced in oil-cracking operations which comprises introducing such vapors, previously freed of constituents having boiling points higher than are normally included in gasoline, into the lower portion of a condensing and rectifying zone, withdrawing reflux condensate from said zone, cooling it and returning it at a higher level in said zone as a cooling and refluxing medium therefor, delivering another stream of reflux condensate from said first-mentioned rectifying zone into a second rectifying zone, the lower portion of which is heated to a temperature sufficient to effect stabilization of the gasoline condensate passing therethrough, delivering vapors liberated in said second rectitying zone to said first-mentioned rectifying zone, delivering vapors from said first-mentioned rectifying zone into a third rectifying zone wherein condensation and rectification of gasoline co nstituents'
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- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
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- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Description
Patented Nov. 12, 1940 UNITED. STATES PATENT OFFICE FRACTIONATION OF HYDROCARBON VAPOR I MIXTURE S Gerald L. Eaton, Osborne, Pa., assignor to Gulf Oil Corporation, Pittsburgh, Pa., a corporation of Pennsylvania Application October 31,, 1938, Serial No. 238,029 1 Claim. (Cl. 19611) 3 as are produced in processes of cracking hydrocarbon oils.
As is well known, the products obtained in oilcracking processes contain, in addition to constituents having boiling points above the normal gasoline boiling-point range, considerable quantitles of normally gaseous materials such as butane, butylenes, propane, propylene, ethane, ethylene, methane and hydrogen. The separation of the higher boiling members of this series from gasoline constitutes a definite problem in the art, a problem which has been made somewhat more critical by the development of processes for effecting cracking and polymerization of C3 and C4 hydrocarbons to gasoline-like materials. If the gasoline hydrocarbons are removed from the vapors by simple condensation, sharp separation is impossible; either the condensed gasoline is highly unstable and contains undesirable quantities of normally gaseous materials or an undesirable amount of hydrocarbons having 5 or more carbon atoms per molecule remains uncondensed. I
It is usually desired to retain a certain amount of the C4 hydrocarbons in thestabilized gaso line, the exact amount depending upon the vapor pressure specifications for gasoline, which, of course, vary in accordance, with the seasons. It will be obvious that if this entails a failure to condense C5 and heavier hydrocarbons, considerable inefiiciency will result, and where, as is now frequently the case, it is desired to deliver the higher boiling constituents of the uncondensed gases to a cracking or polymerizing zone, the presence of C5 and heavier hydrocarbonsin the mixture thus delivered is undesirable.
In the prior applications of Povl Ostergaard, Serial No. 52,717, filed December 3, 1935 and Serial No. 103,947, filed October 3, 1936, there are described and claimed certain improvements in fractionating hydrocarbon vapors of the character referred to hereinabove, comprising a combined condenser-stabilizer for removing stabilized gasoline from hydrocarbon gases containing the same, such as the gases leaving the main gas-oil fractionator of an oil cracking unit either of conventional type or of the so-called gas-reversion or gas-recycling type. This combined condenser-stabilizer essentially consists of two fractionating columns normally superimposed one upon the other, with means for introducing hy-- drocarbon vapors of thecharacter described at a point intermediate'the two columns. The upper column serves primarily as a condenser and dephlegmator wherein the vapors are contacted with cool reflux condensate. This reflux medium is obtained by withdrawing unstabilized gasoline condensate from the intermediate portion of the tower, cooling it and recirculating it tothe upper portion of the condensing column. Exl 0 cess unstabilized condensate drawn from the base of the condensing'column is delivered to the lower or stabilizing column, and heat is supplied to the base of the stabilizing, column, usually through the medium of a boiler of more or less l e. conventional type. During its passage downwardly through the stabilizing column, the condensate from the upper or condensing column is rectified and stabilized, the vapors liberated during stabilization being returned to the upper or condensing column.
The above system has proved extremely advantageous in practice, as a means for recovering stabilized condensate from oil-cracking units, both of conventional type and of the so-called 25 gas-reversion type. It has certain very important practical advantages over a simple rectifying column of conventional type as Well as over other prior art devices. One of these advantages resides in the fact that cooling is efiected at a 30 higher temperature level than is true of the ordinary rectifying column. To illustrate this more fully, it will be remembered that in the ordinary rectifying column as applied to vapors of this type, some form of cooling is provided at the top of the column. This may be either a small coil located in the head of the column, or it may comprise a separate condenser receiving vapors from the top of the column, together with means for recirculating condensate thereby obtained into the head of the column. In order for such a rectifying column to work efficiently, a temperature differential must be maintained throughout the column and this means that the 45 temperatures of the outlet vapors will be low, not far removed from atmospheric. This in turn means that temperature differential between the vapors leaving the top of the column and the recycled reflux is'low; and it is difiicult to supply adequate cooling on account of this low ter'nperature difierential. In the Ostergaard condenser-stabilizer, on the other hand, the stabilized condensate which is to be returned as reflux is withdrawn from an inter+ mediate portion of the column at a temperature substantially higher than that maintained in the upper portion of the column, so that there is a very large temperature differential between the temperature of the side stream as withdrawn from the column and the temperature of the same material when returned as reflux; this vastly increases the ease and economy of operation.
The Ostergaard system also has the advantage that the cooling is applied to a liquid stream rather than to a vapor stream and is somewhat more efficient on that account.
It must be conceded, however, that notwithstanding the definite practical advantages of the Ostergaard condenser-stabilizer, there is a slight theoretical disadvantage in the Ostergaard system as specifically shown in the aforesaid prior applications. For utmost efficiency of fractionation, regardless of other considerations, a rectifying column should be truly countercurrent in principle, with a uniform gradual equilibrium change from trayto tray through the entire column. It will be obvious that withdrawal of a side stream from the column and return of this side stream aiter cooling to a high point in the column involves some theoretical upsetting of the equilibrium conditions within the tower, for it is obvious that the side stream or reflux cannot be precisely in equilibrium with the vapors at the point of re-entry into the column. The vapors at the point of re-entry should contain considerably less of the higher boiling constituents present than the vapors and liquid at the point of withdrawal. Consequently, the reflux material in the Ostergaard system inevitably contains a slightly higher proportion of high boiling, i. e. gasoline, constituents thanis desirable for utmost fractionatingefiiciency.
It will be understood, of course, that theoretical fractionating efficiency is'not always the most important consideration. There are many instances in which designs embodying some slight variation from theoretical fractionating efflstabilizer.
ciency are found to be of practical advantage under given conditions and that is true of the Ostergaard system.
I have found that the advantages of the Ostergaard system may be retained, and a more nearly perfect theoretical fractionating efliciency attained, by a simple modification of the Ostergaard system.
In accordance withmy invention, mixed hydrocarbon vapors of the character referred to hereinabove, such as vapors produced in the cracking of hydrocarbon oils from which constituents heavier than gasoline have been removed, are introduced into a condenser-stabilizer column differing from the Ostergaard column in that three instead of two sections are provided. The two lower sections are substantially identical in construction and operation to the two sections of the Ostergaard condenser- I-Iowever, I also provide a third section superimposed upon the intermediate or condensing section and provided with means for condensing or dephlegmating the vapors reaching the top of this third section to produce a condensate which is then returned to the head of the third section as a cooling and reflux medium therefor.
The bulk of the cooling is. supplied by withdrawing a side stream and returning it to the tem. Additional cooling and rectification is,
however, provided in the upper or third section, the primary purpose being to correct any lack of proper equilibrium at the top of the intermediate section and thereby to insure that all normallyliquid constituents desired to be included in the stabilized gasoline fraction are condensed and held within the column and do not pass out in uncondensed form.
This system is of especial advantage in all instances where the character of the vapors is such that use of the Ostergaard system tends to leave a small amount of gasoline constituents uncondensed in the overhead product from the column.
In order that my invention may be more clearly set forth and understood, I now describe, with reference to the drawing illustrating and forming part of this specification, various preferred forms and manners in which my invention may be practiced and embodied. In the drawing, I
The single figure is a more or less'diagrammatical and conventionalized elevational viewof a condensing and stabilizing column, adaptedfor the performance of the process of my invention.
Referring to this drawing, a mixture of hydro carbon vapors containing gasolinev constituents and lighter normally gaseous constituents are shown entering the system through a line I. In a preferred specific embodimentof the invention, these vapors constitute the overhead product from the main fractionator (not shown) of an oil cracking or gas polymerization unit, being free or substantially free from constituents boiling above the normal gasoline boiling-point range and containing, in addition to hydrocarbons having boiling points within the gasoline boiling-point range, considerable quantities of lower boiling constituents, such as hydrocarbons having not more than four carbon atoms per molecule.
These vapors are first introduced into an indirect heat exchanger or cooler 2 wherein their temperature is substantially reduced. The partly cooled vapor is then passed through a line 3 into the lower part of a fractionating column 4 which, as shown, comprises the mid-section of a fractionating column also having upper and lower sections 5 and 6, respectively. Each of the sections 4, 5 and 6 is internally provided with a weir device 8 is provided between the mid-sec- A tion 4 and the lower or stabilizing section 6. A
suitable weir device, as illustrated in the drawing, is provided with a vapor conduit 9 and a liquid downflow pipe ll].
Relatively cool reflux oil, obtained as set forth hereinbelow, is introduced into the upper portion of the mid-section 4 through a line 12. As the vapors pass upward though the mid-section 4, they are met by a descending flow of relatively cool reflux condensate introduced as aforesaid, resulting in the condensation of unstabilized gasoline, which collects in the weir device 8. A portion of the condensate thus obtained is withdrawn from the weir device 8 through a line l3 having, a valve l4 and is delivered through a line l5 to an indirect cooler l6. The cooled condensate leaving the cooler I6 passes through a line I! to a pump l8 which in turn delivers it to the line [2 into the upper portion of the midsection 4.
Alternatively, reflux for the midsection 4 may be provided by withdrawing faportion of the internal reflux from a trap tray or weir device 19 located above the point of introduction of the vapors into the mid-section 4. Reflux condensate thus withdrawn passes through a line 20 having a valve 2| and communicating with the line l5, and is cooled in the cooler l6 before being returned by the pump l8'through the line l2 into the upper part of the mid-section 4, as before.
Unstabilized condensate collecting in the weir device 8 and not withdrawn through the pipe l3 passes through the downflow pipe l6 into the lower or stabilizing section 6 of the column, the base of which is in communication through a valved liquid line 23 and a vapor-return line 24 with a re-boiler 25 of conventional design. The re-boiler 25 is provided with an internal coil 26 or other means for supplying heat thereto. Stabilized gasoline is withdrawn from the bottom of the re-boiler 25 through an outlet line 21 having a valve 28.
During its passage downwardly through the lower section 6, the unstabilized condensate is rectified and stabilized to remove constituents too light to be included in the final gasoline product. These constituents, in vapor form, re-enter the mid-section 4 through the vapor line 9.
Vapors uncondensed in the mid-section 4 pass upward into the upper section 5 of the column, where they are subjected to further cooling and rectification. In the instance shown, such cool-- ing and refluxing is effected by withdrawing uncondensed vapors from the top of the column through a line 30 leading to a condenser 3|, which in turn communicates through a line 32 with a vapor-separator 33. Condensate collecting in the separator 33, as a result of the cooling effected in the cooler 31, is withdrawn through a line 34 leading to a pump 35, which in turn delivers the cool reflux condensate through a line 36 into the top of the upper section 5 of the column.
In passing upward through the column 5, the vapors from the mid-section 4, undergo further rectification, the temperature and amount of reflux supplied being sufilcient to prevent the escape from the top of the column in uncondensed form of constituents desired to be retained in the final gasoline product. Thus any C5 hydrocarbons which are retained in the reflux supplied through the line l2 and which may be vaporized in the upper portion of the mid-section 4 are condensed and held back in the upper section 5 of the column.
While the specific temperatures maintained at different points in the unit will vary in accordance with the results desired and in accordance with the character of the vapors charged, the following temperatures, observed in connection with a typical operating instance, will serve to illustrate and exemplify my invention. more specifically:
F. Vapors entering through line 1 389 Vapors passing through line 3 285 Side stream, where withdrawn through line 13 n 250 Side stream, where withdrawn through line 20 184 Reflux returning through line 12 Vapors leaving through line 30 173 Reflux returning through line 36 100 Stabilized gasoline withdrawn through line 27 470 Pressure 330 pounds per square inch gage.
For convenience these temperatures have been indicated on the drawing, but it will be understood from the foregoing that they are merely illustrative and are not to be construed as limiting the invention to this specific instance.
The foregoing temperatures were observed in connection with an operation in which 6205 mols per hour of vapors of the character indicated were supp-lied through the line I. From these vapors there was recovered 1250 mols per hour of stabilized gasoline free from C3 hydrocarbons and containing 8.1 per cent by volume of C4 hydrocarbons. The net overhead vapors leaving the separator 33 through the line 31 amounted to 4955 mols per hour, constituted as follows:
Whereas the stabilized distillate in this instance amounted to 500 barrels per hour, the reflux supplied through the line l2 amounted to 915 barrels per hour, and the reflux supplied through the line 36 amounted to 450 barrels per hour.
From [the above figures, it will be evident that my invention makes it possible to obtain a remarkable sharp separation of stabilizedgasoline from vapors of the character indicated. Propane is entirely excluded from the stabilized gasoline, while the net overhead products contain an exceptionally small percentage of C5 and heavier hydrocarbons.
As will be evident from an inspection of the temperatures given in connection with the specific example described, the major portion of cooling required for the tower is supplied in the condenser [6, where the temperature drop is large as compared with the temperature drop through the cooler 3 l. Where the cooler 2 is dispensed with, a still larger temperature drop in the cooler l6 will occur.
While I have described my invention hereinabove with respect to a preferred form and embodiment, for purposes of illustration and exempliflcation, and with respect to a specific operating example, it will be understood by those skilled in the art that my invention is not limited to the details thereof, but may variously be practiced and embodied within the scope of the claims hereinafter made.
What I claim is:
A method of condensing stabilized gasoline from vapors comprising a mixture of hydrocarbons having boiling points within a gasoline boiling-point range and hydrocarbons having lower boiling points, such as are produced in oil-cracking operations, which comprises introducing such vapors, previously freed of constituents having boiling points higher than are normally included in gasoline, into the lower portion of a condensing and rectifying zone, withdrawing reflux condensate from said zone, cooling it and returning it at a higher level in said zone as a cooling and refluxing medium therefor, delivering another stream of reflux condensate from said first-mentioned rectifying zone into a second rectifying zone, the lower portion of which is heated to a temperature sufficient to effect stabilization of the gasoline condensate passing therethrough, delivering vapors liberated in said second rectitying zone to said first-mentioned rectifying zone, delivering vapors from said first-mentioned rectifying zone into a third rectifying zone wherein condensation and rectification of gasoline co nstituents'in the vapors entering from the firstmentioned rectifying zone is effected, withdrawing uncondensed vapors from the upper portion of said third rectifying zone, cooling said vapors to condense the heavier portions thereof, returningat least a portion of the condensate thereby obtained to the said third rectifying zone as a cooling and refluxing medium and in such quantities and at such a temperature as to efieot condensation from the vapors traversing said third rectifying zone of substantially all gasoline hydrocarbons contained therein, and returning reflux condensate from said third rectifying zone to said first-mentioned rectifying zone.
GERALD L. EATON.
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US238020A US2221702A (en) | 1938-10-31 | 1938-10-31 | Fractionation of hydrocarbon vapor mixtures |
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US238020A US2221702A (en) | 1938-10-31 | 1938-10-31 | Fractionation of hydrocarbon vapor mixtures |
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2646392A (en) * | 1949-04-29 | 1953-07-21 | Universal Oil Prod Co | Apparatus for fractionating multicomponent streams |
US3136706A (en) * | 1960-06-20 | 1964-06-09 | Phillips Petroleum Co | Optimum fractionation and steam production |
US3296121A (en) * | 1964-06-15 | 1967-01-03 | Phillips Petroleum Co | Distillation control system |
US4776948A (en) * | 1984-01-30 | 1988-10-11 | Williams, Phillips & Umphlett | Fractionation method with quench liquid recycle |
US4964980A (en) * | 1988-07-27 | 1990-10-23 | Amoco Corporation | Apparatus and process for stabilizing liquid hydrocarbon condensate |
-
1938
- 1938-10-31 US US238020A patent/US2221702A/en not_active Expired - Lifetime
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2646392A (en) * | 1949-04-29 | 1953-07-21 | Universal Oil Prod Co | Apparatus for fractionating multicomponent streams |
US3136706A (en) * | 1960-06-20 | 1964-06-09 | Phillips Petroleum Co | Optimum fractionation and steam production |
US3296121A (en) * | 1964-06-15 | 1967-01-03 | Phillips Petroleum Co | Distillation control system |
US4776948A (en) * | 1984-01-30 | 1988-10-11 | Williams, Phillips & Umphlett | Fractionation method with quench liquid recycle |
US4964980A (en) * | 1988-07-27 | 1990-10-23 | Amoco Corporation | Apparatus and process for stabilizing liquid hydrocarbon condensate |
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