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US3633371A - Gas separation - Google Patents

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US3633371A
US3633371A US719032A US3633371DA US3633371A US 3633371 A US3633371 A US 3633371A US 719032 A US719032 A US 719032A US 3633371D A US3633371D A US 3633371DA US 3633371 A US3633371 A US 3633371A
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gas
ethane
line
feed
absorbing
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US719032A
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Joseph W Davison
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Phillips Petroleum Co
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    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F25REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
    • F25JLIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
    • F25J3/00Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification
    • F25J3/02Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream
    • F25J3/0228Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream characterised by the separated product stream
    • F25J3/0238Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream characterised by the separated product stream separation of CnHm with 2 carbon atoms or more
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C7/00Purification; Separation; Use of additives
    • C07C7/005Processes comprising at least two steps in series
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C7/00Purification; Separation; Use of additives
    • C07C7/11Purification; Separation; Use of additives by absorption, i.e. purification or separation of gaseous hydrocarbons with the aid of liquids
    • 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
    • C10G5/00Recovery of liquid hydrocarbon mixtures from gases, e.g. natural gas
    • C10G5/04Recovery of liquid hydrocarbon mixtures from gases, e.g. natural gas with liquid absorbents
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F25REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
    • F25JLIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
    • F25J3/00Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification
    • F25J3/02Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream
    • F25J3/0204Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream characterised by the feed stream
    • F25J3/0209Natural gas or substitute natural gas
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F25REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
    • F25JLIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
    • F25J3/00Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification
    • F25J3/02Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream
    • F25J3/0228Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream characterised by the separated product stream
    • F25J3/0233Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream characterised by the separated product stream separation of CnHm with 1 carbon atom or more
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F25REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
    • F25JLIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
    • F25J3/00Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification
    • F25J3/02Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream
    • F25J3/0228Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream characterised by the separated product stream
    • F25J3/0247Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream characterised by the separated product stream separation of CnHm with 4 carbon atoms or more
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F25REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
    • F25JLIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
    • F25J2205/00Processes or apparatus using other separation and/or other processing means
    • F25J2205/02Processes or apparatus using other separation and/or other processing means using simple phase separation in a vessel or drum
    • F25J2205/04Processes or apparatus using other separation and/or other processing means using simple phase separation in a vessel or drum in the feed line, i.e. upstream of the fractionation step
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F25REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
    • F25JLIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
    • F25J2205/00Processes or apparatus using other separation and/or other processing means
    • F25J2205/50Processes or apparatus using other separation and/or other processing means using absorption, i.e. with selective solvents or lean oil, heavier CnHm and including generally a regeneration step for the solvent or lean oil

Definitions

  • GAS SEPARATION This invention relates to a new and improved method for recovering ethane from a normally gaseous material.
  • maximum recovery of ethane from a normally gaseous material at minimum cost per volume of ethane recovered is achieved by first cooling the gaseous material to a temperature in the range of from about 70 to about l F said temperature being sufficient to liquefy a portion of said gaseous material and thereby produce an ethane and heavier rich liquid, separating the liquid from the remaining, uncondensed gas, and then contacting at least a portion of the remaining gas with an absorbent as hereinafter defined to remove additional ethane from the gas, the absorbing step being carried out at a temperature in the range of from about 70 to about-120 F.
  • the procedure of this invention a maximum amount of ethane is recovered from a gas in the most economic manner because the refrigerating step is employed only to the extent that it remains economical based on the amount of the ethane recovered thereby, and thereafter additional ethane is recovered by using a less expensive absorbing step.
  • the absorbing step is carried out on the already refrigerated gas thereby obtaining maximum benefit of (l) the refrigeration step since the absorbent is, because of its refrigerated condition, in a state of increased capacity for ethane and also since the ethane is tending toward liquefaction, and (2) the function of the absorbent.
  • the ethane produce of this invention can be dehydrogenated using known procedures and the resulting ethylene employed as a monomer in known polymerization procedures to produce polyethylene.
  • the polyethylene so produced is useful for making with known techniques such as blow molding a wide variety of articles of commerce such as bottles, e. g., baby bottles, wastepaper baskets, and the like.
  • the drawing shows a system which embodies this invention.
  • line 1 which carries the feed to the system.
  • the feed can be any conventional ethane-containing gas such as natural gas or a gasoline plant residue gas. Such gases are well known in the art.
  • the feed gas can contain at least 50 volume percent of methane, ethane, and propane, the remainder being essentially butane and heavier saturated and unsaturated normally gaseous hydrocarbons, nitrogen, carbon dioxide, helium, water, and the like. The amount of water present should not be sufficient to cause plugging of the apparatus by the formation of ice crystals.
  • the methane, ethane, and propane present in the feed gas are each present in substantial amounts. For example, of a mixture of methane, ethane, and propane present in the feed gas, at least 50 volume percent can be methane, the remainder being from about 5 to about 25 volume percent each of ethane and propane.
  • the feed in line 1 passes to heat exchanger 2 which can be composed of one or more conventional heat exchange units and/or one or more conventional refrigeration units.
  • the heat exchange system 2 is designed to cool the feed gas to a temperature in the range of from about -70 to about 1 20 F.
  • recycle gas in line 3 can pass through the system. This is advantageous because it conserves refrigeration expenses by utilizing the already cooled gas after it is through the absorbing treatment, thereby cooling the feed and also heating the already treated gas before it is passed to a pipeline or other disposition by way of line 4. It should be noted that the feed gas can be cooled in heat exchange system 2 by a combination of cooling steps such as by first being cooled by coming in heat exchange relationship with already treated and refrigerated gas in line 3, and thereafter being further cooled by other heat exchange relationships and/or refrigeration processes which are not related to nor dependent upon the use ofthe gas in line 3.
  • the cooling step should reduce the temperature of the feed gas into the range set forth hereinabove, and should also liquefy at least a portion of that feed gas, preferably from about 5 to about volume percent of the feed gas being processed.
  • This partial liquefaction step in the temperature range recited will produce an ethane and heavier rich liquid in contact with a methane rich gas.
  • This gas also contains recoverable amounts of ethane.
  • the partially condensed feed stream then passes by way of line 5 to separator 6 wherein the uncondensed gas is allowed to separate and collect at the top of the separator and the liquified portion of the feed gas is allowed to collect at the bottom of the separator and is removed by way of line 7.
  • the liquid removed by way of line 7 is rich in ethane and heavier hydrocarbons.
  • This liquid can be subjected to a conventional demethanization distillation process to remove any methane present in the liquid, thereby leaving a liquid consisting essentially of ethane, propane, and any heavier components that happen to be in the feed gas and that boil at temperatures higher than propane.
  • the demethanized liquid can then be subjected to another distillation step wherein substantially pure ethane is recovered as an overhead product.
  • the overhead product from separator 6 passes by way of line 8 and line 9 into absorbing zone 10. It is important to maintain the refrigerated status of the overhead gas passing into absorbing zone 10 in order to make the most advantage of the prior refrigeration step when carrying out the absorbing step. If in the transfer of the overhead gas from separator 6 to absorbing zone 10 the gas happens to be heated to a temperature outside of the range of 70 to -l20 F. an additional cooling system 11 can be employed to cool that gas so that the gas in the absorbing zone 10 is at a temperature in the range of from about 70 to about 1 20 F.
  • the gas in absorbing zone 10 tends to pass upwardly and in so doing is contacted countercurrently with downwardly passing absorbing liquid from line 12.
  • the absorbent employed is precooled to substantially the same temperature as the gas present in the absorbing zone, and therefore is at a temperature in the range of from about 70 to about l20 F.
  • the absorbent employed is a liquid at the temperature of the gas present in the absorbing zone and consists essentially of saturated hydrocarbons having from four to eight carbon atoms per molecule, inclusive, preferably hexanes such as normal hexane. Mixtures of these hydrocarbons can be employed also.
  • Feed A contains about 3.4 mol percent the high capacity of the absorbent for ethane at low tempera- 5 ethane, the remainder being essentially methane, propane and tures.
  • Feed B is under pressure of 500 p.s.i.a. is to 80 volume percent of the ethane present in the feed gas can cooled in heat exchange system 2 to a temperature of about be obtained at costs substantially less than using other a 70 F., and then passed to separation zone 6. Part of the techniques such as absorption or partial condensation by themselves I overhead gas from separation zone 6 is passed to absorption zone 10. During this passage the gas is cooled to about 80 F. Separator 6 can be operated at a pressure substantially the before being passed into the absorption zone. The absorbent, same as the pressure of the feed gas in line 1, taking into acagain consisting essentially of normal hexane, is precooled to a count pressure drops caused by friction and the like in transtemperature of about 80 F.
  • absorbing zone 10 can also be operated at substantially the same pressure as the pressure in in both runs, the pressures in separation zone 6 and absorbseparator 6 also taking into account normal pressure drop ocing zone 10 are substantially the same as the initial 500 p.s.i.a. curring in lines 8 and 9, and cooling system 11 ifpresent. pressure of the feed allowing of course for normal pressure
  • separator 6 can be operated as a flash unit in drop in the pipes due to friction and the like. that the pressure maintained in that separator can be substan-
  • the results of the runs are as follows:
  • feed gas consists essentially of a finite amount up to 25 volume percent ethane, the remainder being essentially methane and propane; and the absorbent consists essentially of normal hexane.

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  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Physics & Mathematics (AREA)
  • General Engineering & Computer Science (AREA)
  • Thermal Sciences (AREA)
  • Mechanical Engineering (AREA)
  • General Chemical & Material Sciences (AREA)
  • Water Supply & Treatment (AREA)
  • Analytical Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Separation By Low-Temperature Treatments (AREA)

Abstract

A method for recovering ethane and heavier from a normally gaseous material by partially condensing the gas by cooling to a temperature in the range of from about -70* to about -120* F., removing uncondensed gas with an absorbent at a temperature in the range of from about -70* to about -120* F.

Description

United States Patent [72] Inventor Joseph W. Davison Bartlesville, Okla. [2]] Appl. No. 719,032 [22] Filed Apr. 5, 1968 [45] Patented Jan. 11, 1972 73] Assignee Phillips Petroleum Company [54] GAS SEPARATION 4 Claims, 1 Drawing Fig.
2,603,310 7/1952 Gilmore 62/17 Redcay Koble Mc1ntire.... Davison.....
Napoli.... Miller Primary ExaminerNorman Yudkoff Assistant Examiner-Arthur F. Purcell Attorney- Young and Quigg ABSTRACT: A method for recovering ethane and heavier from a normally gaseous material by partially condensing the gas by cooling to a temperature in the range of from about 70 to about 120 F., removing uncondensed gas with an absorbent at a temperature in the range of from about -70 to about -l 20 F.
GAS SEPARATION This invention relates to a new and improved method for recovering ethane from a normally gaseous material.
Heretofore cooling gases to at least partially condense same has been used as a type of a reverse distillation procedure.
According to this invention maximum recovery of ethane from a normally gaseous material at minimum cost per volume of ethane recovered is achieved by first cooling the gaseous material to a temperature in the range of from about 70 to about l F said temperature being sufficient to liquefy a portion of said gaseous material and thereby produce an ethane and heavier rich liquid, separating the liquid from the remaining, uncondensed gas, and then contacting at least a portion of the remaining gas with an absorbent as hereinafter defined to remove additional ethane from the gas, the absorbing step being carried out at a temperature in the range of from about 70 to about-120 F.
By this procedure separation of ethane by liquefaction thereof is practiced to the point where maximum amounts of ethane as well as heavier hydrocarbons are liquefied and past which point the additional ethane liquefied would not be worth the cost of obtaining the necessary lower temperatures, i.e., the cost of the additional refrigeration necessary. After the cooling step the nonliquefied gaseous portion can be treated with certain absorbents while still in the temperature range of from about 70 to about l20 F. and additional ethane thereby recovered from the gas. In this manner maximum ethane recovery is achieved by using the partial condensation technique only to the extent that the amount of ethane recovered thereby justifies the refrigeration cost and thereafter still more ethane is recovered by a less expensive absorbing step. It is important to note that the absorbing step is carried out in the temperature range of from about 70 to about 1 20 F. since this procedure insures maximum removal of ethane by the absorbent.
By the procedure of this invention, a maximum amount of ethane is recovered from a gas in the most economic manner because the refrigerating step is employed only to the extent that it remains economical based on the amount of the ethane recovered thereby, and thereafter additional ethane is recovered by using a less expensive absorbing step. However, the absorbing step is carried out on the already refrigerated gas thereby obtaining maximum benefit of (l) the refrigeration step since the absorbent is, because of its refrigerated condition, in a state of increased capacity for ethane and also since the ethane is tending toward liquefaction, and (2) the function of the absorbent.
The ethane produce of this invention can be dehydrogenated using known procedures and the resulting ethylene employed as a monomer in known polymerization procedures to produce polyethylene. The polyethylene so produced is useful for making with known techniques such as blow molding a wide variety of articles of commerce such as bottles, e. g., baby bottles, wastepaper baskets, and the like.
Accordingly, it is an object of this invention to provide a new and improved process for separating ethane from normally gaseous materials.
It is another object of this invention to provide a new and improved process for removing a maximum amount of ethane from a gas at minimum cost by utilizing partial condensation techniques to the extent that they remain economic and thereafter using an absorbing step on the already refrigerated gases, thereby taking advantage of the increased efficiency of the refrigeration and absorbing steps at the same time in the absorbing step.
Other aspects, objects and the several advantages of this invention will become apparent from a study of the disclosure, drawing and appended claims.
The drawing shows a system which embodies this invention.
in the drawing, there is shown line 1 which carries the feed to the system.
The feed can be any conventional ethane-containing gas such as natural gas or a gasoline plant residue gas. Such gases are well known in the art. Generally, the feed gas can contain at least 50 volume percent of methane, ethane, and propane, the remainder being essentially butane and heavier saturated and unsaturated normally gaseous hydrocarbons, nitrogen, carbon dioxide, helium, water, and the like. The amount of water present should not be sufficient to cause plugging of the apparatus by the formation of ice crystals. The methane, ethane, and propane present in the feed gas are each present in substantial amounts. For example, of a mixture of methane, ethane, and propane present in the feed gas, at least 50 volume percent can be methane, the remainder being from about 5 to about 25 volume percent each of ethane and propane.
The feed in line 1 passes to heat exchanger 2 which can be composed of one or more conventional heat exchange units and/or one or more conventional refrigeration units. The heat exchange system 2 is designed to cool the feed gas to a temperature in the range of from about -70 to about 1 20 F.
As shown in the drawing, recycle gas in line 3 can pass through the system. This is advantageous because it conserves refrigeration expenses by utilizing the already cooled gas after it is through the absorbing treatment, thereby cooling the feed and also heating the already treated gas before it is passed to a pipeline or other disposition by way of line 4. It should be noted that the feed gas can be cooled in heat exchange system 2 by a combination of cooling steps such as by first being cooled by coming in heat exchange relationship with already treated and refrigerated gas in line 3, and thereafter being further cooled by other heat exchange relationships and/or refrigeration processes which are not related to nor dependent upon the use ofthe gas in line 3.
The cooling step should reduce the temperature of the feed gas into the range set forth hereinabove, and should also liquefy at least a portion of that feed gas, preferably from about 5 to about volume percent of the feed gas being processed. This partial liquefaction step in the temperature range recited will produce an ethane and heavier rich liquid in contact with a methane rich gas. This gas also contains recoverable amounts of ethane.
The partially condensed feed stream then passes by way of line 5 to separator 6 wherein the uncondensed gas is allowed to separate and collect at the top of the separator and the liquified portion of the feed gas is allowed to collect at the bottom of the separator and is removed by way of line 7.
The liquid removed by way of line 7 is rich in ethane and heavier hydrocarbons. This liquid can be subjected to a conventional demethanization distillation process to remove any methane present in the liquid, thereby leaving a liquid consisting essentially of ethane, propane, and any heavier components that happen to be in the feed gas and that boil at temperatures higher than propane. The demethanized liquid can then be subjected to another distillation step wherein substantially pure ethane is recovered as an overhead product.
The overhead product from separator 6 passes by way of line 8 and line 9 into absorbing zone 10. It is important to maintain the refrigerated status of the overhead gas passing into absorbing zone 10 in order to make the most advantage of the prior refrigeration step when carrying out the absorbing step. If in the transfer of the overhead gas from separator 6 to absorbing zone 10 the gas happens to be heated to a temperature outside of the range of 70 to -l20 F. an additional cooling system 11 can be employed to cool that gas so that the gas in the absorbing zone 10 is at a temperature in the range of from about 70 to about 1 20 F.
The gas in absorbing zone 10 tends to pass upwardly and in so doing is contacted countercurrently with downwardly passing absorbing liquid from line 12.
The absorbent employed is precooled to substantially the same temperature as the gas present in the absorbing zone, and therefore is at a temperature in the range of from about 70 to about l20 F. The absorbent employed is a liquid at the temperature of the gas present in the absorbing zone and consists essentially of saturated hydrocarbons having from four to eight carbon atoms per molecule, inclusive, preferably hexanes such as normal hexane. Mixtures of these hydrocarbons can be employed also.
The downwardly passing absorbent very readily absorbs ethane from the upwardly passing refrigerated gas because of ing and using different feed compositions for each run. The two different feeds are denoted herein as Feed A and Feed B, and the compositions of these feeds are given in detail hereinbelow in table I. Feed A contains about 3.4 mol percent the high capacity of the absorbent for ethane at low tempera- 5 ethane, the remainder being essentially methane, propane and tures. Thus the contacting of the thus-refrigerated ethane with heavier hydrocarbons; while Feed B contains about 12 mol the liquid absorbent maximizes the removal of ethane from percent ethane, the remain er being essen a ly h n the gas into the absorbent. propane, and heavier hydrocarbons. The absorbent employed The liquid absorbent rich in ethane is removed by way of Consists S F Y OfnOrmal heXanB. line 13 for further treatment such as distillation to remove Feed A is passed under pressure of 500 p.sia to cooling ethane therefrom as an overhead product. 0
system 2, cooled to a temperature of about -90 F., and The combination of ethane removed by way of lines 7 and 13 t th th d t f d thereafter passed into separation zone 6. A portion of the cons I u es 6 e ane Pro uc 0 1S mven an WI overhead gas from separation zone 6 is passed into absorption generally represent from about 5 to about 95 volume percent a zone 10 and therein is at a temperature of about -80 F. The of the ethane present in the feed gas in line 1. By following the absorbent is passed into absorption zone 10 also at a temperaprocedure of this invention an ethane extraction as deep as 70 o ture of about -80 F. Feed B is under pressure of 500 p.s.i.a. is to 80 volume percent of the ethane present in the feed gas can cooled in heat exchange system 2 to a temperature of about be obtained at costs substantially less than using other a 70 F., and then passed to separation zone 6. Part of the techniques such as absorption or partial condensation by themselves I overhead gas from separation zone 6 is passed to absorption zone 10. During this passage the gas is cooled to about 80 F. Separator 6 can be operated at a pressure substantially the before being passed into the absorption zone. The absorbent, same as the pressure of the feed gas in line 1, taking into acagain consisting essentially of normal hexane, is precooled to a count pressure drops caused by friction and the like in transtemperature of about 80 F. and is passed into the absorbing porting the feed gas through the refrigeration system 2 and zone 10 into separator 6. Similarly, absorbing zone 10 can also be operated at substantially the same pressure as the pressure in in both runs, the pressures in separation zone 6 and absorbseparator 6 also taking into account normal pressure drop ocing zone 10 are substantially the same as the initial 500 p.s.i.a. curring in lines 8 and 9, and cooling system 11 ifpresent. pressure of the feed allowing of course for normal pressure Alternatively, separator 6 can be operated as a flash unit in drop in the pipes due to friction and the like. that the pressure maintained in that separator can be substan- The results of the runs are as follows:
TABLE I 1 7 9 12 13 14 17 Feed A:
Methane 252, 358 3,305.5 224,147.2 0 32,364.7 191,782.5 24,905.3 Ethane 8, 976 781. 7, 375. 1 0 6,030. 4 1, 344. 7 819. 5 Propane 2, 666 1, 265. 2 1, 260. 7 0 1, 260. 7 0 140. 1 n-Hexane 0 0 0 30, 000 29, 546 454 0 Feed B:
Methane 224,440 16,908. 9 186,778 0 26, 303.3 160, 474.7 20, 753. 1 Ethane 31,680 11,241.3 18, 394.8 0 12, 988.8 5,406 2,043. 0 I Propane 7, 920 6, 360. 7 1, 403. 3 0 1, 403. 3 155. ll Il-HeXane 0 0 0 30,000 29, 300.7 699.3 0
l Mols per day. The number heading the column corresponds to the reference number found in the drawing. For example, the column headed 1 stands for the composition of the maten'al in line 1 oi the drawing.
tially less than the pressure of the feed gas in line 1, thereby Reasonable variations and modifications are possible within causing partial volatilization of the liquid passing into separat e Scope of th s d sc osure wi hout departing from the spirit tor 6 and additional temperature reduction. This partial and scope thereflfvolatilization will decrease the amount of methane carried by iclaimi the liquid that passes from the separator by way of line 7. A P Comprising Providing a feed gas containing at Generally, the pressure decrease in Separator 6 below the least volume percent ofa mixture ofsubstantial amounts of pressure of the feed gas in line 1 is at least 10 p.s.i.g., each of methane Fthane, and Propane; cooling Said feed gas preferably from about 10 to about 100 p.s.i.g. In this embodito a temperature in the range of from about to about ment, the absorbing zone 10 is maintained at a pressure sub- Sald temperature and Suitable Pressure being Surfistantially the same as reduced pressure in separator 6. Clem to llquefy from about 5 to about 95 Volume P of Apart of the overhead gas in line 8 and all of the overhead gas in line 14 can be disposed of at will such as by reheating and passing to a pipeline or other storage facility. However, for maximum economics, all of the refrigerated, overhead gas in line 14 is passed through lines 15, 16, and 3 into heat exchange relationship with the incoming feed gas from line 1 as discussed hereinabove. In addition, if desired, a portion of the refrigerated, overhead gas in line 8 can be passed through line 17 into line 16 and thereby through line 3 into the heat exchange system 2 to also serve to cool the incoming feed gas from line 1. Normally, substantially all of he overhead gas in line 8 is passed through line 9 into absorbing zone 10. However, any portion or all of the overhead gas in line 8 can be passed into line 17. Preferably, at least 5 volume percent of the gas in line 8 passes into line 9 for treatment in absorbing zone [0.
EXAMPLE Two runs are made using the apparatus shown in the drawsaid gas and thereby produce an ethane and heavier rich liquid; separating said ethane rich liquid from the remaining unliquefied gas in a separation zone; separately removing from said separation zone said unliquefied gas and said ethane rich liquid and thereafter recovering ethane from said ethane rich liquid as a product of the process and not returned thereto; passing at least a portion of the unliquefied gas which was separated from said ethane rich liquid to an absorbing zone which is maintained at a temperature in the range of from about 70 to about l20 F contacting said unliquefied gas in said absorbing zone with a precooled absorbent which is liquid at the temperature maintained in said absorbing zone and which consists, essentially of saturated hydrocarbons having from four to eight carbon atoms per molecule, inclusive; separately removing from said absorbing zone gas rich in methane and liquid absorbent rich in ethane and thereafter separately recovering ethane from said liquid absorbent rich in ethane as a product of the process and not returned thereto.
2. The method according to claim 1 wherein said gas and liquid separating step and said absorbing step are each carried liquid separation step.
4. A method according to claim 1 wherein said feed gas consists essentially of a finite amount up to 25 volume percent ethane, the remainder being essentially methane and propane; and the absorbent consists essentially of normal hexane.
UNITED STATES PATENT OFFICE CERTIFICATE OF QQRREQTIQN Patent No. 3,633,371 Dated anuary l1 19 72 N Inventor(s) Joseph Davlson It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:
Column 5, line 4 (claim 3), before "s ubstantially" insert pressure Signed and sealed this 30th day of May 1972.
(SEAL) Attest:
EDWARD M.FLETCHER,JR.
ROBERT GOTTSCHALK Attesting Officer Commissioner of Patents FORM PO-1050 (10-69) USCOMM-DC 6O378-P69 & U,S. GOVERNMENT PRINTING OFFICE: I969 0-868"!!!

Claims (3)

  1. 2. The method according to claim 1 wherein said gas and liquid separating step and said absorbing step are each carried out at substantially the same pressure as the initial pressure of said feed gas.
  2. 3. A method according to claim 1 wherein said gas and liquid separating step is carried out at a substantially lower than the initial pressure of said feed gas to cause flashing of a part of the liquefied feed gas, and said absorbing step is carried out at substantially the same pressure as said gas and liquid separation step.
  3. 4. A method according to claim 1 wherein said feed gas consists essentially of a finite amount up to 25 volume percent ethane, the remainder being essentially methane and propane; and the absorbent consists essentially of normal hexane.
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Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4035167A (en) * 1976-02-13 1977-07-12 Continental Oil Company Recovery of ethane and ethylene from gaseous mixtures
US4525187A (en) * 1984-07-12 1985-06-25 Air Products And Chemicals, Inc. Dual dephlegmator process to separate and purify syngas mixtures
US4713940A (en) * 1985-11-07 1987-12-22 Linde Aktiengesellschaft Process for obtaining C2+ or C3+ hydrocarbons from gaseous mixtures
US4717408A (en) * 1986-08-01 1988-01-05 Koch Process Systems, Inc. Process for prevention of water build-up in cryogenic distillation column
USRE32600E (en) * 1983-01-14 1988-02-16 Koch Process Systems, Inc. Distillative separation employing bottom additives
US5150279A (en) * 1991-03-18 1992-09-22 International Business Machines Corporation High performance computer system with platters and unidirectional storage modules therebetween
US5261250A (en) * 1993-03-09 1993-11-16 Polycold Systems International Method and apparatus for recovering multicomponent vapor mixtures
US5462583A (en) * 1994-03-04 1995-10-31 Advanced Extraction Technologies, Inc. Absorption process without external solvent
US5502971A (en) * 1995-01-09 1996-04-02 Abb Lummus Crest Inc. Low pressure recovery of olefins from refinery offgases
WO2003002921A1 (en) * 2001-06-29 2003-01-09 Exxonmobil Upstream Research Company Process for recovering ethane and heavier hydrocarbons from a methane-rich pressurized liquid mixture
US20080087041A1 (en) * 2004-09-14 2008-04-17 Denton Robert D Method of Extracting Ethane from Liquefied Natural Gas

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US2603310A (en) * 1948-07-12 1952-07-15 Phillips Petroleum Co Method of and apparatus for separating the constituents of hydrocarbon gases
US2765635A (en) * 1952-08-07 1956-10-09 Gulf Oil Corp Process for separation of gases
US2775103A (en) * 1954-12-23 1956-12-25 Phillips Petroleum Co Hydrocarbon separation
US2815650A (en) * 1955-07-01 1957-12-10 Phillips Petroleum Co Reboiled absorber operation
US2933901A (en) * 1955-12-19 1960-04-26 Phillips Petroleum Co Separation of fluid mixtures
US3247649A (en) * 1963-04-29 1966-04-26 Union Oil Co Absorption process for separating components of gaseous mixtures
US3359743A (en) * 1966-04-29 1967-12-26 Nat Distillers Chem Corp Low temperature process for the recovery of ethane from a stripped natural gas stream

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Publication number Priority date Publication date Assignee Title
US2603310A (en) * 1948-07-12 1952-07-15 Phillips Petroleum Co Method of and apparatus for separating the constituents of hydrocarbon gases
US2765635A (en) * 1952-08-07 1956-10-09 Gulf Oil Corp Process for separation of gases
US2775103A (en) * 1954-12-23 1956-12-25 Phillips Petroleum Co Hydrocarbon separation
US2815650A (en) * 1955-07-01 1957-12-10 Phillips Petroleum Co Reboiled absorber operation
US2933901A (en) * 1955-12-19 1960-04-26 Phillips Petroleum Co Separation of fluid mixtures
US3247649A (en) * 1963-04-29 1966-04-26 Union Oil Co Absorption process for separating components of gaseous mixtures
US3359743A (en) * 1966-04-29 1967-12-26 Nat Distillers Chem Corp Low temperature process for the recovery of ethane from a stripped natural gas stream

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4035167A (en) * 1976-02-13 1977-07-12 Continental Oil Company Recovery of ethane and ethylene from gaseous mixtures
USRE32600E (en) * 1983-01-14 1988-02-16 Koch Process Systems, Inc. Distillative separation employing bottom additives
US4525187A (en) * 1984-07-12 1985-06-25 Air Products And Chemicals, Inc. Dual dephlegmator process to separate and purify syngas mixtures
US4713940A (en) * 1985-11-07 1987-12-22 Linde Aktiengesellschaft Process for obtaining C2+ or C3+ hydrocarbons from gaseous mixtures
US4717408A (en) * 1986-08-01 1988-01-05 Koch Process Systems, Inc. Process for prevention of water build-up in cryogenic distillation column
US5150279A (en) * 1991-03-18 1992-09-22 International Business Machines Corporation High performance computer system with platters and unidirectional storage modules therebetween
US5261250A (en) * 1993-03-09 1993-11-16 Polycold Systems International Method and apparatus for recovering multicomponent vapor mixtures
US5462583A (en) * 1994-03-04 1995-10-31 Advanced Extraction Technologies, Inc. Absorption process without external solvent
US5551972A (en) * 1994-03-04 1996-09-03 Advanced Extraction Technologies, Inc. Absorption process without external solvent
US5502971A (en) * 1995-01-09 1996-04-02 Abb Lummus Crest Inc. Low pressure recovery of olefins from refinery offgases
WO2003002921A1 (en) * 2001-06-29 2003-01-09 Exxonmobil Upstream Research Company Process for recovering ethane and heavier hydrocarbons from a methane-rich pressurized liquid mixture
US6564580B2 (en) 2001-06-29 2003-05-20 Exxonmobil Upstream Research Company Process for recovering ethane and heavier hydrocarbons from methane-rich pressurized liquid mixture
US20080087041A1 (en) * 2004-09-14 2008-04-17 Denton Robert D Method of Extracting Ethane from Liquefied Natural Gas
US8156758B2 (en) 2004-09-14 2012-04-17 Exxonmobil Upstream Research Company Method of extracting ethane from liquefied natural gas

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