US2952984A - Processing liquefied natural gas - Google Patents

Processing liquefied natural gas Download PDF

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US2952984A
US2952984A US743732A US74373258A US2952984A US 2952984 A US2952984 A US 2952984A US 743732 A US743732 A US 743732A US 74373258 A US74373258 A US 74373258A US 2952984 A US2952984 A US 2952984A
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Prior art keywords
natural gas
vapors
liquefied natural
methane
fractionating zone
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US743732A
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Jr Walton H Marshall
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Conch International Methane Ltd
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Conch International Methane Ltd
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Priority to BE579774D priority Critical patent/BE579774A/xx
Priority to NL240371D priority patent/NL240371A/xx
Application filed by Conch International Methane Ltd filed Critical Conch International Methane Ltd
Priority to US743732A priority patent/US2952984A/en
Priority to GB19587/59A priority patent/GB854099A/en
Priority to DEC19159A priority patent/DE1122560B/en
Priority to FR797889A priority patent/FR1228634A/en
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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
    • F25J3/0204Processes 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
    • F25J3/0214Liquefied natural gas
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C7/00Purification; Separation; Use of additives
    • C07C7/04Purification; Separation; Use of additives by distillation
    • 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
    • C10G5/06Recovery of liquid hydrocarbon mixtures from gases, e.g. natural gas by cooling or compressing
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10KPURIFYING OR MODIFYING THE CHEMICAL COMPOSITION OF COMBUSTIBLE GASES CONTAINING CARBON MONOXIDE
    • C10K1/00Purifying combustible gases containing carbon monoxide
    • C10K1/04Purifying combustible gases containing carbon monoxide by cooling to condense non-gaseous materials
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F17STORING OR DISTRIBUTING GASES OR LIQUIDS
    • F17CVESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
    • F17C9/00Methods or apparatus for discharging liquefied or solidified gases from vessels not under pressure
    • F17C9/02Methods or apparatus for discharging liquefied or solidified gases from vessels not under pressure with change of state, e.g. vaporisation
    • F17C9/04Recovery of thermal energy
    • 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
    • F25J3/0238Processes 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
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F17STORING OR DISTRIBUTING GASES OR LIQUIDS
    • F17CVESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
    • F17C2265/00Effects achieved by gas storage or gas handling
    • F17C2265/05Regasification
    • 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
    • F25J2200/00Processes or apparatus using separation by rectification
    • F25J2200/02Processes or apparatus using separation by rectification in a single pressure main column system
    • 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
    • F25J2200/00Processes or apparatus using separation by rectification
    • F25J2200/74Refluxing the column with at least a part of the partially condensed overhead 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
    • F25J2270/00Refrigeration techniques used
    • F25J2270/04Internal refrigeration with work-producing gas expansion loop

Definitions

  • This invention relates generally to improvements in the art of distributing and processing natural gas, and more particularly, but not by way of limitation, to an improved method of preparing liquefied natural gas for use as a fuel, or partly for use as a fuel and partly for use as raw material in the petrochemical industry.
  • the liquefied natural gas is revaporized and used as a fuel.
  • the natural gas can be revaporized and used directly as a fuel.
  • the gas specifications for existing equipment therein are different from the specifications of the revaporized natural gas, thereby requiring that the rev-aporized natural gas be reformed to a lower heating value and new specific gravity before use.
  • natural gas usually contains a rather wide range of hydrocarbons.
  • methane comprises the major proportion of the natural gas, with the heavier hydrocarbons such as ethane, propane, butane and the like being present in the gas in minor proportions. At least some of these heavier hydrocarbons can be separated before the natural gas is liquefied and transported to the remote localities.
  • These heavier hydrocarbons have two important uses at the remote localities.
  • the heavier hydrocarbons may be conveniently used in the formation of a carrier gas having a lower heating value and new specific gravity, with the carrier gas being subsequently mixed with methane to form the gaseous fuel having the desired heat content and specific gravity specificaitons.
  • the heavier hydrocarbons may be economically used as a raw material in the petrochemical industry in the remote locality.
  • the present invention contemplates a novel method of separating the methane and heavier hydrocarbons in liquefied natural gas, with a simultaneous revaporization of the methane.
  • the revaporization and separation are accomplished in a fractionating zone in such a manner that a portion of the heat in vapors withdrawn from the fractionating zone may be efiiciently utilized in heating the liquefied natural gas fed to the fractionating zone, and the resulting vapors will be extremely rich in methane, i.e., containing a very minor proportion of the heavier hydrocarbons.
  • Condensate formed in said vapors by passage in heat exchange relation with the liquefied natu- 2,952,984 Patented Sept.
  • the present method also contemplates the recovery of work from the separated methane, as well as the utilization of heat from the expanded methane vapors for Warming methane vapors being fed to the work-producing zone, such that the maximum energy of the separated methane may be utilized.
  • the separated heavier hydrocarbons may be used either in forming a carrier gas or as a raw material in the petrochemical industry, as previously indicated.
  • An important object of this invention is to provide an efficient method of separating methane from a liquefied natural gas with a minimum of equipment and cost.
  • Another object of this invention is to simultaneously separate methane fromliquefied natural gas and revapon'ze the methane.
  • a further object of this invention is to provide a novel method of fractionating liquefied natural gas, wherein the overhead from the fractionating zone is utilized to heat the liquefied natural gas being fed to the fractionating zone.
  • a still further object of this invention is to recover power in a process of revaporizing liquefied natural gas.
  • the single figure of the drawing is a flow diagram illustrating a practice of this invention.
  • natural gas ordinarily cornprises a rather wide range of hydrocarbons, and it is desirable that all of the hydrocarbons be liquefied prior to transporting the composition to a remote locality.
  • the liquefied naural gas to be separated and revaporized has the following analysis, although it will be understood that this composition is merely an example and. that the invention may be practiced with a liquefied natural gashaving substantially any composition:
  • reference character 10 designates a line leading from a sourcev (not shown) of the liquefied natural gas, which will ordinarily be a suitable insulated storage tank located in a coastal region where the liquefied natural gas may be received from similar insulated containers mounted aboard a ship used in transporting the gas to the remote locality-
  • the liquefied natural gas is ordinarily stored at. about atmospheric pressure, or slightly above, with a temperature of about 246 F. to 258 F., depending upon the precise composition of the gas.
  • This low pressure and cold liquefied gas is fed to a pump. 12 for pumping the liquefied natural gas through another line 14 to a fractionating tower 16 at increased pressure.
  • the pump 12 provide a substantial increase in the pressure of the liquefied natural gas, with the pressure being raised to about 585 p.s.i.g. to facilitate fractionation and subsequent power recovery, as, will be more fully hereinafter set forth.
  • a pair of heat exchangers 18 and 20 are interposed in the line 14 to. heat the liquefied natural gas being fed to the fractionating tower 16 3 until approximately the bubble point temperature of the liquefied natural gas is reached.
  • the liquefied natural gas being fed to the tower 16 is pressurized and then heated to approximately its bubble point.
  • the fractionating tower 16 may be of any desired con struction which provides a vertically extended fractionating zone.
  • the liquefied natural gas is, fed to the medial portion of the tower 16 and is slightly expanded, as from 585 p.s.i.g. to 535 p.s.i.g. into the tower 16 to facilitate separation of the methane from the heavier hydrocarbons.
  • the liquid accumulating in the lower end portion of the tower 16 is circulated through a re-boilcr 22 for heating the tower to such a temperature that methane enriched vapors will be directed into the upper portion of the tower, and the liquid in the lower portion of the tower will be enriched with the heavier hydrocarbons.
  • the liquid in the lower portion of the tower 16 is heated to a temperature of about 135 F. by the re-boiler 22.
  • the reboiler22 derives its heat from any suitable heating medium, such as a gaseous product from a reforming operation, to maintain the desired temperature of the liquid in the lower portion of the tower 16.
  • the liquid accumulating in the lower portion of the tower 16 is selectively withdrawn through a line 24 to maintain the desired liquid level in the tower.
  • a typical analysis of liquid withdrawn through the line 24 is as follows:
  • This liquid withdrawn through line'24 will, of course, be at the same pressure as the tower 16 and ata temperature of about 135 F. It is preferred that the liquid be passed through a suitable expansion valve 26 for at least partially vaporizing the liquid and reducing the pressure thereof to a pressure suitable for transportation through a pipeline 28 to the point of use. As previously indicated, these heavier hydrocarbons may be conveniently used in forming a carrier gas by a reforming operation or used as a raw material in a petrochemical industry.
  • the methane enriched vapors rising to the upper portion of the fractionating tower 16 are withdrawn through a'line 30 and passed through the heat exchanger 18 interposed in the liquefied natural gas feed line 14.
  • a typical analysis of the vapors withdrawn through the line 30 is as follows:
  • the vapors withdrawn through the line 30 will be at about 535 p.s.i.g. and l18 F.
  • the vapors will be cooled to about l20 F., whereas the liquefied natural gas will be slightly warmed to enhance the subsequent fractionation there of. Cooling of the methane enriched vapors directed through the line 30 condenses a' portion of the vapors. Therefore, the vapors are directed through a line 32 from the heat exchanger 18 into an accumulator 34 which also functions as a separator for collecting the condensates in the lower portion thereof. These condensates are refluxed to the upper portion of the tower 16 through a line 35. The refluxed condensates will'be at about 120 from the heavier hydrocarbons in the tower 16.
  • the refluxed condensates will'be at about 120 from the heavier hydrocarbons in the tower 16.
  • the vapors discharged through the line 36 will be at about 535 p.s.i.g. and about -l20 F. These vapors are passed through a series of heat exchangers 38, 40 and 42 to provide a substantial warming of the vapors. It is preferred that thermethane vapors be warmed by passage through the heat exchangers 38, 40 and 42 to a temperature of about 700 F. whereupon, the gas is expanded through a suitable expander 44 down to aboutp.s.i.g. for the recovery of a substantial amount of work from the revaporized methane.
  • the device 44 may be of any suitable form, such as a turbine, which will form a work-producing zone throughwhich the methane may be expanded to produce work.
  • the expander 44 should produce about 7400 B.H.P.; whereas the pump 12 for increasing :the'pressure of the liquefield natural gas will require only about 790 B.H.P., thereby resulting in a substantial power recovery, from the system.
  • the exhaust from the expander 44 is fed through a line 46 to the heat exchanger 40 to provide heating of the feed to the expander, as previously described.
  • the revaporized methane may be used directly as a fuel, or reformed to a lower heat content and new specific gravity, as previously indicated;
  • the revaporized methane discharging from the heat exchanger 40 will be at about 100 p.s.i.g. and 100 F.
  • the methane vapors passing from the line 36 to the heat exchanger 38 on their way to the expander 44 are initially heated by a heating medium passed through the heat exchanger 38.
  • the heating medium passed through the heat exchanger 38 may be of any suitable form having a temperature higher than the temperature of the methane vapors in the line 36.
  • the heating medium for the heat exchanger 38 may conveniently be a hot fluid from the reforming operation.
  • the heating medium passed through the heat exchanger 38 should have a temperature of about 81 F. This heating medium may then be transferred through a line 48 to the heat exchanger 20 used for heating the liquefied natural gas being fed to the fractionating tower 16.
  • the present invention provides an efiicient method for separating methane from liquefied natural gas by using the minimum of apparatus, and with a minimum of cost. It will be further apparent that the separation of the methane from the heavier hydrocarbon components of a liquefied natural gas stream is accomplished simultaneously with revaporization of the methane, such that the separted components will be in proper form for use as a fuel or for further processing. The method may be performed in such a manner that a substantial amount of work may be recovered from the revaporized methane.
  • the present invention provides a novel method of fractionating liquefield gases, wherein the overhead vapors from the fractionating zone are passed in heat exchange relation with the liquefied gases being fed to the fractionating zone, and wherein the resulting condensates are refluxed to the fractionating zone, to provide an efficient fractionation without the necessity of using a separate reflux condenser and refrigerant.
  • a method as defined in claim 1 characterized further in heating the liquefied natural gas being fed to the fractionating zone to such an extent that said feed is approximately at its bubble point upon entering the fractionating zone.
  • a method as defined in claim 1 characterized further in expanding said methane enriched vapors, after removal of the condensates therefrom, through a workproducing zone.
  • a method as defined in claim 1 characterized further in compressing the liquefied natural gas being fed to the fractionating zone.
  • a method as defined in claim 1 characterized further in compressing the liquefied natural gas being fed to the fractionating zone, and heating the compressed liquefied natural gas to approximately its bubble point temperature.
  • a method as defined in claim 6 characterized further in passing the expanded vapors in heat exchange relation with said vapors between removal of condensates from said vapors and expansion of said vapors.
  • a method as defined in claim 6 characterized further in heating the liquefied natural gas being fed to the fractionating zone to approximately the bubble point temperature thereof.
  • a method as defined in claim 6 characterized further in that the liquefied natural gas being fed to the fractionating zone is raised in pressure to about 585 p.s.i.g and heated to its bubble point temperature before entering the fractionating zone.
  • a method as defined in claim 6 characterized further in heating said vapors to about 700 F. before expansion in said work-producing zone.
  • a method of separating the lower boiling temperature component from a liquefied gas mixture by use of a fractionating tower the improvement which comprises feeding the liquefied gas mixture into the medial portion of the tower, re-boiling the contents of the lower portion of the tower to such a temperature to produce vapors enriched with the lower boiling temperature component in the upper portion of the tower, directly passing said vapors in heat exchange relation with the liquefied gas mixture being fed to the tower, separating condensates from said vapors, and refluxing said condensates back to the upper portion of the tower.

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Description

p 1960 w. H. MARSHALL, JR 2,952,984
PROCESSING LIQUEFIED NATURAL GAS Filed June 23, 1958 A Trap/VH6 2,952,984 PROCESSING LIQUEFIED NATURAL GAS Walton H. Marshall, Jr., Downings, Va., assignor, by mesne assignments, to Conch International Methane Limited, a corporation of the Bahamas Filed June 23, 1958, 'Ser. No. 743,732 11 'Claims. (Cl. 62-27) This invention relates generally to improvements in the art of distributing and processing natural gas, and more particularly, but not by way of limitation, to an improved method of preparing liquefied natural gas for use as a fuel, or partly for use as a fuel and partly for use as raw material in the petrochemical industry.
As it is well known in the art, some localities have an abundant supply of natural gas, whereas other localities have very little or no natural gas resources. When such localities are reasonably close to one another, the natural gas may be transported from one locality to the other by means of a pipeine. However, when such localities are separated by long distances, or by substantial bodies of water, transportation by pipeline becomes impractical. A new industry is in the stage of development for the pri mary purpose of liquefying natural gas in a locality having an abundant supply and transporting the natural gas in liquefied form to a remote locality having a natural gas shortage. The liquefied natural gas occupies about the space required for natural gas in gaseous form, thereby making transportation over long distances practical. At the remote locality, the liquefied natural gas is revaporized and used as a fuel. In some of these remote localities, the natural gas can be revaporized and used directly as a fuel. In other localities, the gas specifications for existing equipment therein are different from the specifications of the revaporized natural gas, thereby requiring that the rev-aporized natural gas be reformed to a lower heating value and new specific gravity before use.
As it is also known in the art, natural gas usually contains a rather wide range of hydrocarbons. Ordinarily, methane comprises the major proportion of the natural gas, with the heavier hydrocarbons such as ethane, propane, butane and the like being present in the gas in minor proportions. At least some of these heavier hydrocarbons can be separated before the natural gas is liquefied and transported to the remote localities. However, it is sometimes desirable to liquefy the heavier hydrocarbons along with the methane and transport the entire natural gas composition to the remote locality in liquid form. These heavier hydrocarbons have two important uses at the remote localities. Firstly, when the natural gas must be reformed to a lower heating value and new specific gravity to meet existing equipment specifications, the heavier hydrocarbons may be conveniently used in the formation of a carrier gas having a lower heating value and new specific gravity, with the carrier gas being subsequently mixed with methane to form the gaseous fuel having the desired heat content and specific gravity specificaitons. Secondly, the heavier hydrocarbons may be economically used as a raw material in the petrochemical industry in the remote locality.
The present invention contemplates a novel method of separating the methane and heavier hydrocarbons in liquefied natural gas, with a simultaneous revaporization of the methane. The revaporization and separation are accomplished in a fractionating zone in such a manner that a portion of the heat in vapors withdrawn from the fractionating zone may be efiiciently utilized in heating the liquefied natural gas fed to the fractionating zone, and the resulting vapors will be extremely rich in methane, i.e., containing a very minor proportion of the heavier hydrocarbons. Condensate formed in said vapors by passage in heat exchange relation with the liquefied natu- 2,952,984 Patented Sept. 20, 1960 ral gas are refluxed to the fractionating zone to enhance the separation of methane in the fiactionating zone. The present method also contemplates the recovery of work from the separated methane, as well as the utilization of heat from the expanded methane vapors for Warming methane vapors being fed to the work-producing zone, such that the maximum energy of the separated methane may be utilized. The separated heavier hydrocarbons may be used either in forming a carrier gas or as a raw material in the petrochemical industry, as previously indicated.
An important object of this invention is to provide an efficient method of separating methane from a liquefied natural gas with a minimum of equipment and cost.
Another object of this invention is to simultaneously separate methane fromliquefied natural gas and revapon'ze the methane.
A further object of this invention is to provide a novel method of fractionating liquefied natural gas, wherein the overhead from the fractionating zone is utilized to heat the liquefied natural gas being fed to the fractionating zone. I
A still further object of this invention is to recover power in a process of revaporizing liquefied natural gas.
Other objects and advantages of the invention will be evident from the following detailed description, when read in conjunction with the accompanying drawing which illustrates this invention.
The single figure of the drawing is a flow diagram illustrating a practice of this invention.
As previously indicated, natural gas ordinarily cornprises a rather wide range of hydrocarbons, and it is desirable that all of the hydrocarbons be liquefied prior to transporting the composition to a remote locality. To illustratethe present invention, it will be assumed that the liquefied naural gas to be separated and revaporized has the following analysis, although it will be understood that this composition is merely an example and. that the invention may be practiced with a liquefied natural gashaving substantially any composition:
Referring to the drawing in detail, reference character 10 designates a line leading from a sourcev (not shown) of the liquefied natural gas, which will ordinarily be a suitable insulated storage tank located in a coastal region where the liquefied natural gas may be received from similar insulated containers mounted aboard a ship used in transporting the gas to the remote locality- The liquefied natural gas is ordinarily stored at. about atmospheric pressure, or slightly above, with a temperature of about 246 F. to 258 F., depending upon the precise composition of the gas. This low pressure and cold liquefied gas is fed to a pump. 12 for pumping the liquefied natural gas through another line 14 to a fractionating tower 16 at increased pressure. It is preferred that the pump 12 provide a substantial increase in the pressure of the liquefied natural gas, with the pressure being raised to about 585 p.s.i.g. to facilitate fractionation and subsequent power recovery, as, will be more fully hereinafter set forth. Also, a pair of heat exchangers 18 and 20 are interposed in the line 14 to. heat the liquefied natural gas being fed to the fractionating tower 16 3 until approximately the bubble point temperature of the liquefied natural gas is reached. In other words, the liquefied natural gas being fed to the tower 16 is pressurized and then heated to approximately its bubble point. The detailed operations of the heat exchangers 18 and 20 are described in detail below.
The fractionating tower 16 may be of any desired con struction which provides a vertically extended fractionating zone. The liquefied natural gas is, fed to the medial portion of the tower 16 and is slightly expanded, as from 585 p.s.i.g. to 535 p.s.i.g. into the tower 16 to facilitate separation of the methane from the heavier hydrocarbons. The liquid accumulating in the lower end portion of the tower 16 is circulated through a re-boilcr 22 for heating the tower to such a temperature that methane enriched vapors will be directed into the upper portion of the tower, and the liquid in the lower portion of the tower will be enriched with the heavier hydrocarbons. In the example used for illustration, the liquid in the lower portion of the tower 16 is heated to a temperature of about 135 F. by the re-boiler 22. The reboiler22 derives its heat from any suitable heating medium, such as a gaseous product from a reforming operation, to maintain the desired temperature of the liquid in the lower portion of the tower 16. The liquid accumulating in the lower portion of the tower 16 is selectively withdrawn through a line 24 to maintain the desired liquid level in the tower. A typical analysis of liquid withdrawn through the line 24 is as follows:
Component: Mol. percent Methane 1.0 Ethane 45.7 Propane 32.1 Isobutaue 7.7 n-Butane 7.9' Isopentane 2.4 n-Pentane 1.2 Benzene 1.2 n-Heptane 0.8
This liquid withdrawn through line'24 will, of course, be at the same pressure as the tower 16 and ata temperature of about 135 F. It is preferred that the liquid be passed through a suitable expansion valve 26 for at least partially vaporizing the liquid and reducing the pressure thereof to a pressure suitable for transportation through a pipeline 28 to the point of use. As previously indicated, these heavier hydrocarbons may be conveniently used in forming a carrier gas by a reforming operation or used as a raw material in a petrochemical industry.
The methane enriched vapors rising to the upper portion of the fractionating tower 16 are withdrawn through a'line 30 and passed through the heat exchanger 18 interposed in the liquefied natural gas feed line 14. A typical analysis of the vapors withdrawn through the line 30 is as follows:
Also, with the temperature and pressure conditions previously indicated in the tower 16, the vapors withdrawn through the line 30 will be at about 535 p.s.i.g. and l18 F. When these vapors are passed through the heat exchanger 18, the vapors will be cooled to about l20 F., whereas the liquefied natural gas will be slightly warmed to enhance the subsequent fractionation there of. Cooling of the methane enriched vapors directed through the line 30 condenses a' portion of the vapors. Therefore, the vapors are directed through a line 32 from the heat exchanger 18 into an accumulator 34 which also functions as a separator for collecting the condensates in the lower portion thereof. These condensates are refluxed to the upper portion of the tower 16 through a line 35. The refluxed condensates will'be at about 120 from the heavier hydrocarbons in the tower 16. The
condensates being refluxed to the tower 16 will be enriched with methane, but will contain an appreciable proportion of heavier hydrocarbons. A typical analysis is:
Component: Mol. percent Methane 97.81 Ethane 2.19
On the other hand, the vapors withdrawn through a line 36 from the top of the refiuxaccumulaltor 34 will have a smaller percentage of heavier hydrocarbons, with a typical analysis thereof being as follows:
Component: 7 Mol. percent Methane 99.05 Ethane 1 0.95
It may also be noted that the vapors discharged through the line 36 will be at about 535 p.s.i.g. and about -l20 F. These vapors are passed through a series of heat exchangers 38, 40 and 42 to provide a substantial warming of the vapors. It is preferred that thermethane vapors be warmed by passage through the heat exchangers 38, 40 and 42 to a temperature of about 700 F. whereupon, the gas is expanded through a suitable expander 44 down to aboutp.s.i.g. for the recovery of a substantial amount of work from the revaporized methane. The device 44 may be of any suitable form, such as a turbine, which will form a work-producing zone throughwhich the methane may be expanded to produce work. In a typical installation, where about 255,398 pounds per/hr. of liquefied natural gas are fed to the tower 16, and having a composition as previously described, the expander 44 should produce about 7400 B.H.P.; whereas the pump 12 for increasing :the'pressure of the liquefield natural gas will require only about 790 B.H.P., thereby resulting in a substantial power recovery, from the system.
The exhaust from the expander 44 is fed through a line 46 to the heat exchanger 40 to provide heating of the feed to the expander, as previously described. After the revaporized methane has been passed through the heat exchanger 40, it may be used directly as a fuel, or reformed to a lower heat content and new specific gravity, as previously indicated; In the example disclosed, the revaporized methane discharging from the heat exchanger 40 will be at about 100 p.s.i.g. and 100 F.
The methane vapors passing from the line 36 to the heat exchanger 38 on their way to the expander 44 are initially heated by a heating medium passed through the heat exchanger 38. The heating medium passed through the heat exchanger 38 may be of any suitable form having a temperature higher than the temperature of the methane vapors in the line 36. When the present method is being used in combination with a reforming process, the heating medium for the heat exchanger 38 may conveniently be a hot fluid from the reforming operation. For the temperature and pressure conditions previously described, the heating medium passed through the heat exchanger 38 should have a temperature of about 81 F. This heating medium may then be transferred through a line 48 to the heat exchanger 20 used for heating the liquefied natural gas being fed to the fractionating tower 16. It will be understood, however, that separate heating mediums may be used in the exchangers 20 and 38, it being only necessary that the liquefield natural gas being fed to the tower 16 be raised approximately to its bubble point temperature, and the revaporized methane in the line 36 be raised to a temperature for eflicient heat transfer with the expanded methane vapors in the line 46;
' When it is desired to heat the revaporized methane in the line 36 to a temperature which will provide the most eflicient expansion of the methane through the expander 44 and permit use of this expanded methane for heat exchange relation with the feed to the expander, it is required that an additional heating medium of rather high temperature be passed through the heat exchanger 42. Any desired heating medium may be used with the heat exchanger 42, it only being necessary that the revaporized methane being fed to the expander 44 be increased in temperature for an eflicient expansion. When the present method is being used in combination with a reforming operation, a hot gas from the reforming operation at about 840 F. may be passed through the heat exchanger 42. Thus, the revaporized methane may be raised to a temperature of about 700 F. before passing through the expander 44.
From the foregoing it will be apparent that the present invention provides an efiicient method for separating methane from liquefied natural gas by using the minimum of apparatus, and with a minimum of cost. It will be further apparent that the separation of the methane from the heavier hydrocarbon components of a liquefied natural gas stream is accomplished simultaneously with revaporization of the methane, such that the separted components will be in proper form for use as a fuel or for further processing. The method may be performed in such a manner that a substantial amount of work may be recovered from the revaporized methane. It will also be apparent that the present invention provides a novel method of fractionating liquefield gases, wherein the overhead vapors from the fractionating zone are passed in heat exchange relation with the liquefied gases being fed to the fractionating zone, and wherein the resulting condensates are refluxed to the fractionating zone, to provide an efficient fractionation without the necessity of using a separate reflux condenser and refrigerant.
Changes may be made in the combination and arrangement of steps and procedures, as well as the form and arrangement of apparatus, heretofore set forth in specification and shown in the drawing, it being understood that changes may be made in the precise embodiment disclosed without departing from the spirit and scope of the invention as defined in the following claims.
We claim:
1. In a method of separating the heavier hydrocarbons from liquefield natural gas containing a substantial proportion of methane, the steps of:
(a) feeding the liquefied natural gas into the medial portion of a fractionating zone,
(b) heating the contents of the lower portion of the fractionating zone to a temperature to produce methane enriched vapors in the upper portion of the fractionating zone,
(c) withdrawing vapors from the upper portion of the fractionating zone and directly passing said vapors in heat exchange relation with the liquefied natural gas being fed to the fractionating zone, to heat said feed and cool said vapors,
(d) separating condensates from said vapors, after they have been used in heat exchange relationship with the liquefied natural gas,
(e) refluxing said condensates to the upper portion of the fractionating zone for cooling the upper portion of the fractionating zone and inducing downward movement of heavier hydrocarbon enriched liquefield gas into the lower portion of the fractionating zone, and
(f) withdrawing the heavier hydrocarbon enriched liquefied gas from the lower portion of the fractionating zone.
2. A method as defined in claim 1 characterized further in heating the liquefied natural gas being fed to the fractionating zone to such an extent that said feed is approximately at its bubble point upon entering the fractionating zone.
3. A method as defined in claim 1 characterized further in expanding said methane enriched vapors, after removal of the condensates therefrom, through a workproducing zone.
4. A method as defined in claim 1 characterized further in compressing the liquefied natural gas being fed to the fractionating zone.
5. A method as defined in claim 1 characterized further in compressing the liquefied natural gas being fed to the fractionating zone, and heating the compressed liquefied natural gas to approximately its bubble point temperature.
6. In a method of separating the heavier hydrocarbons from liquefied natural gas containing a substantial proportion of methane and stored at about atmospheric pressure, the steps of:
(a) pumping the liquefied natural gas into the medial portion of a fractionating zone at an increased pressure,
(b) heating the lower portion of the fractionating zone to a temperature to produce methane enriched vapors in the upper portion of the fractionating zone,
(c) withdrawing the methane enriched vapors from the upper portion of the fractionating zone and directly passing said vapors in heat exchange relation with the pressurized liquefied natural gas being fed to the fractionating zone for heating said feed and cooling said vapors,
(d) separating the condensates from said vapors, after they have been used in heat exchange relationship with the liquefied natural gas.
(e) refluxing said condensates to the upper portion of the fractionating zone to cool the upper portion of the fractionating zone and enhance the accumulation of heavier hydrocarbon enriched liquid in the lower portion of the fractionating zone,
(f) withdrawing liquid from the lower portion of the fractionating zone, and
(g) expanding said vapors, after removal of said condensates, through a work-producing zone.
7. A method as defined in claim 6 characterized further in passing the expanded vapors in heat exchange relation with said vapors between removal of condensates from said vapors and expansion of said vapors.
8. A method as defined in claim 6 characterized further in heating the liquefied natural gas being fed to the fractionating zone to approximately the bubble point temperature thereof.
9. A method as defined in claim 6 characterized further in that the liquefied natural gas being fed to the fractionating zone is raised in pressure to about 585 p.s.i.g and heated to its bubble point temperature before entering the fractionating zone.
10. A method as defined in claim 6 characterized further in heating said vapors to about 700 F. before expansion in said work-producing zone.
11. In a method of separating the lower boiling temperature component from a liquefied gas mixture by use of a fractionating tower, the improvement which comprises feeding the liquefied gas mixture into the medial portion of the tower, re-boiling the contents of the lower portion of the tower to such a temperature to produce vapors enriched with the lower boiling temperature component in the upper portion of the tower, directly passing said vapors in heat exchange relation with the liquefied gas mixture being fed to the tower, separating condensates from said vapors, and refluxing said condensates back to the upper portion of the tower.
References Cited in the file of this patent UNITED STATES PATENTS 1,465,599 De Brey Aug. 21, 1923 2,526,996 Crawford Oct. 24, 1950 2,583,090 Cost Jan. 22, 1952 2,600,110 Hachmuth June 10, 1952 2,666,019 Winn Ian. 12, 1954

Claims (1)

1. IN A METHOD OF SEPARATING THE HEAVIER HYDROCARBONS FORM LIQUEFIED NATURAL GAS CONTAINING A SUBSTANTIALLY PROPORTION OF METHANE, THE STEPS OF: (A) FEEDING THE LIQUEFIED NATURAL GAS INTO THE MEDIAL PORTION OF A FRACTIONATING ZONE, (B) HEATING THE CONTENTS OF THE LOWER PORTION OF THE FRACTIONATING ZONE TO A TEMPERATURE TO PRODUCE METHANE ENRICHED VAPORS IN THE UPPER PORTION OF THE FRACTIONATING ZONE, (E) WITHDRAWING VAPORS FROM THE UPPER PORTION OF THE FRACTIONATING ZONE AND DIRECTLY PASSING SAID VAPORS IN HEAT EXCHANGE RELATION WITH THE LIQUEFIED NATURAL GAS BEING FED TO THE FRACTIONATING ZONE, TO HEAT SAID FEED AND COOL SAID VAPORS, (D) SEPARATING CONDENSATES FROM SAID VAPORS, AFTER THEY HAVE BEEN USED IN HEAT EXCHANGE RELATIONSHIP WITH THE LIQUEFIED NATURAL GAS,
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GB19587/59A GB854099A (en) 1958-06-23 1959-06-08 Improved method of processing natural gas
DEC19159A DE1122560B (en) 1958-06-23 1959-06-08 Process for the decomposition of a natural gas consisting of methane and higher-boiling hydrocarbons
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