GB2455462A - Process and Apparatus for Separation of Hydrocarbons and Nitrogen - Google Patents

Process and Apparatus for Separation of Hydrocarbons and Nitrogen Download PDF

Info

Publication number
GB2455462A
GB2455462A GB0905124A GB0905124A GB2455462A GB 2455462 A GB2455462 A GB 2455462A GB 0905124 A GB0905124 A GB 0905124A GB 0905124 A GB0905124 A GB 0905124A GB 2455462 A GB2455462 A GB 2455462A
Authority
GB
United Kingdom
Prior art keywords
stream
fractionation
nitrogen
process according
fractionator
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
GB0905124A
Other versions
GB0905124D0 (en
GB2455462B (en
Inventor
Grant Leigh Johnson
Lee Alan Phillips
Terence Ronald Tomlinson
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Costain Oil Gas and Process Ltd
Original Assignee
Costain Oil Gas and Process Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Costain Oil Gas and Process Ltd filed Critical Costain Oil Gas and Process Ltd
Priority to GB0905124A priority Critical patent/GB2455462B/en
Publication of GB0905124D0 publication Critical patent/GB0905124D0/en
Publication of GB2455462A publication Critical patent/GB2455462A/en
Application granted granted Critical
Publication of GB2455462B publication Critical patent/GB2455462B/en
Priority to EP10755496A priority patent/EP2433075A2/en
Priority to US13/259,355 priority patent/US20120090355A1/en
Priority to PCT/GB2010/050488 priority patent/WO2010109228A2/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • 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
    • F25J3/0257Processes 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 nitrogen
    • 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
    • F25J3/06Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by partial condensation
    • F25J3/063Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by partial condensation characterised by the separated product stream
    • F25J3/0635Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by partial condensation 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
    • F25J3/06Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by partial condensation
    • F25J3/063Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by partial condensation characterised by the separated product stream
    • F25J3/066Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by partial condensation characterised by the separated product stream separation of nitrogen
    • 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
    • F25J2200/04Processes or apparatus using separation by rectification in a dual 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
    • F25J2200/04Processes or apparatus using separation by rectification in a dual pressure main column system
    • F25J2200/06Processes or apparatus using separation by rectification in a dual pressure main column system in a classical double column flow-sheet, i.e. with thermal coupling by a main reboiler-condenser in the bottom of low pressure respectively top of high pressure column
    • 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
    • F25J2200/00Processes or apparatus using separation by rectification
    • F25J2200/78Refluxing the column with a liquid stream originating from an upstream or downstream fractionator column
    • 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
    • F25J2210/00Processes characterised by the type or other details of the feed stream
    • F25J2210/06Splitting of the feed stream, e.g. for treating or cooling in different ways
    • 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
    • F25J2235/00Processes or apparatus involving steps for increasing the pressure or for conveying of liquid process streams
    • F25J2235/60Processes or apparatus involving steps for increasing the pressure or for conveying of liquid process streams the fluid being (a mixture of) hydrocarbons
    • 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
    • F25J2270/02Internal refrigeration with liquid vaporising loop

Landscapes

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

Abstract

The invention provides a process and apparatus for the separation of nitrogen from a gaseous feed 1 comprising a mixture of hydrocarbons and nitrogen gas. The process includes cooling and at least partially condensing the gaseous feed in a first heat exchanger 2, and feeding the cooled mixture to a first fractionation column 8 to produce a nitrogen rich overhead vapour fraction 19 and a hydrocarbon rich liquid fraction 9. The liquid fraction is subjected to a second fractionation process, which includes reboil in a second fractionation column 15 at a lower pressure than the first fractionation column. The overhead vapour 19 from the high pressure column is partially condensed, and separated to provide a further liquid stream 22 which provides reflux to the first fractionation column, and a separated vapour stream 23 which is condensed to provide reflux to the second fractionation column. The hydrocarbon rich liquid fraction 9 is sub-cooled in a second heat exchanger 10 and divided into at least two streams. The first stream being expanded and fed to the second fractionation column, and a second stream being expanded and in heat exchange with the separated vapour stream 23, and which provides reheat before the second stream is fed to the second fractionation column. A hydrocarbon product stream 31 low in nitrogen, and a nitrogen rich stream 28, can then both be removed from the second fractionation column.

Description

Process and Apparatus for Separation of Hydrocarbons and Nitrogen This invention relates to processes and apparatus for the low temperature separation of nitrogen from a gaseous mixture comprising nitrogen gas and hydrocarbons. Such mixtures occur naturally in geological formations and can also result from nitrogen injection as a method of improving oil or gas production. Nitrogen separation may be required as part of an overall processing of gaseous hydrocarbons to meet sales specifications, such as maximum inert content or minimum calorific value.
Low temperature fractionation presents an energy efficient method for the separation of nitrogen from gaseous hydrocarbon streams, in particular gaseous hydrocarbon streams wherein the hydrocarbons comprise predominantly methane, such as natural gas.
Separated nitrogen streams of high purity can be produced, thereby maximising hydrocarbon recovery and, where the nitrogen stream is vented to atmosphere, minimising environmental impact.
Where the nitrogen content is higher than approximately 35 to 40 mol%, a double column arrangement (such as disclosed in US 7,127,915) similar to that used in air separation is conventional and is often the most economical choice considering both capital cost and energy consumption. The columns are typically configured in a stacked arrangement, with the upper fractionation column operating at low pressure, just above atmospheric, and the lower fractionation column operating at high pressure, typically at approximately 27 bar (2700 kPa).
An example of a conventional double column arrangement is shown in Figure 1.
A feed gas (01) is cooled and at least partially condensed in heat exchanger (02). The partially condensed feed (03) is expanded across valve (06) to form a two-phase feed (07) which is fed to a high pressure column (08). The high pressure column (08) separates the two-phase feed (07) into a nitrogen rich overhead vapour fraction (19) and a hydrocarbon rich liquid fraction (09).
The hydrocarbon rich liquid fraction (09) from the high pressure column (08) is sub-cooled in heat exchanger (10) to form stream (12) which is expanded across valve (13) to form a further two-phase feed stream (14) which is fed to an intermediate stage of a low pressure column (15).
The overhead vapour (19) from the high pressure column (08) is fully condensed in heat exchange with boiling liquid at the bottom of the low pressure column (15) in reboil heat exchanger (04). The liquid may either be piped from the bottom tray or packed section, or the reboil heat exchanger (04) may be submerged in the liquid in the sump of the low pressure column (15).
The fully condensed overhead stream (20) is split. A portion is passed as reflux (22) to the high pressure column (08) and a portion (23) is sub-cooled in heat exchangers (10) and (24) to form stream (25) which is expanded across valve (26) and passes as reflux (27) to the low pressure column (15).
A hydrocarbon product (31) with low nitrogen content, from the low pressure column (15), is pumped to an elevated pressure, dependent on the composition and pressure of feed gas (01), and is rewarmed and evaporated in heat exchangers (10) and (02) to form a gaseous product (35), providing the majority of the refrigeration for cooling and condensation of the feed gas (01).
A nitrogen vapour stream (28) with low methane content from the low pressure column (15) is rewarmed in heat exchanger (24) to provide refrigeration for sub-cooling of the nitrogen rich reflux stream and is further rewarmed in heat exchangers (10) and (02).
The purity of the hydrocarbon product (31) from the bottom of the low pressure fractionation column (15) is ensured by provision of sufficient reboil in heat exchange with the overhead vapour from the high pressure column (08) in the reboil heat exchanger (04). Purity of the nitrogen product from the low pressure fractionation column overhead (28) is ensured by conditioning the feed streams to the column and, in particular, providing sufficient flow of nitrogen rich reflux (27).
The pressure drop between high pressure fractionation column (08) and low pressure fractionation column (15) provides the required refrigeration by Joule-Thomson expansion. High purity nitrogen and hydrocarbon streams are withdrawn from the top and bottom of the low pressure fractionation column (15) respectively.
When the nitrogen content of the feed gas to a conventional double column system is lower than approximately 35 mol%, insufficient reflux is normally generated to the low pressure fractionation column to maintain low losses of hydrocarbons with the nitrogen product.
In such cases, options to increase the available reflux include: a) compressing the reject nitrogen stream and recycling it to the feed gas or other part of the process to meet reflux requirements; and b) introducing an upstream pre-separation' system to condition the feed gas to produce a stream suitably enriched in nitrogen to feed to the double column system.
Process selection will be dependent on considerations such as plant capacity, feed gas nitrogen content and variability and feed and product gas pressure. Use of an upstream pre-separation' system is efficient in producing product gas at elevated pressure, hence reducing product gas compression power requirements and may also be preferred when the gaseous feed comprises contaminants such as carbon dioxide and heavy hydrocarbons, which are tolerated at higher levels in the pre-separation system. Inclusion of either a pre-separation system or a nitrogen recycle system does however introduce additional equipment items.
The present invention provides an alternative double column system for the separation of nitrogen from a gaseous mixture comprising nitrogen gas and hydrocarbons which uses improved heat integration to maximise the nitrogen reflux stream and to optimise the feed conditions to the low pressure fractionation column. This provides additional flexibility to process gases having low nitrogen content, for example less than 35 mol%, and potentially as low as 20 mol% without recourse to the use of additional equipment for pre-separation or nitrogen recycling as described above. However, the invention is also useful for the separation of gases having nitrogen content above 35 mol%, with improved separation efficiency being observed in comparison with conventional separation techniques.
The present invention provides a process for the separation of nitrogen from a gaseous feed comprising a mixture of hydrocarbons and nitrogen gas, the process comprising the steps of: (I) cooling and at least partially condensing the gaseous feed; (ii) feeding the cooled and at least partially condensed feed from step (i) to a first fractionation to produce an overhead vapour stream having an enriched nitrogen content and a condensed product having a reduced nitrogen content which is subjected to a second fractionation, which comprises reboil, at a lower pressure than the first fractionation; (iii) partially condensing the overhead vapour stream, and separating to provide a liquid stream, which is used to provide reflux to the first fractionation, and a separated vapour stream, which is condensed to provide reflux to the second fractionation; and (iv) sub-cooling the condensed product of the first fractionation and dividing the resulting sub-cooled product into at least two streams: a first stream being expanded and fed to the second fractionation, and a second stream being expanded and reheated in heat exchange with the separated vapour stream from step (iii) before being fed to the second fractionation; (v) removing a hydrocarbon product stream low in nitrogen from the second fractionation; and (vi) removing a nitrogen rich stream from the second fractionation.
The combination of steps (iii) and (iv) enables separation of feed streams with lower nitrogen content than is feasible with prior art processes, such as the conventional double column arrangement described above.
In particular, partial condensation of the overhead vapour stream from the first fractionation allows the separated vapour stream from step (iii) to be efficiently condensed in heat exchange with reheat of the second stream of the condensed product in step (iv) to provide reflux to the second fractionation. The reheated second stream has an increased vapour fraction and its introduction into the second fractionation provides an increased quantity of stripping vapour to the second fractionation. For a given feed composition, the effect of these steps is to provide improved separation, even for feed compositions comprising less than 35 mol% nitrogen, for example 20 to 35 mol%, while maintaining the overall energy efficiency of the separation process.
As a further advantage, partial condensation of the overhead stream from the first fractionation allows the first fractionation and the second fractionation steps to be decoupled' as there is no physical requirement for the second fractionator to be elevated above the first fractionator.
In a preferred embodiment, the hydrocarbons in the gaseous feed comprise or consist of methane. For instance, the gaseous feed may comprise or consist of natural gas. In further preferred embodiments, the gaseous feed comprises less than 40 mol% nitrogen, less than 35 mol% nitrogen, or less than 30 mol% nitrogen. Preferably, the gaseous feed comprises at least 20 mol% nitrogen. The gaseous feed may further comprise other inert gases, such as helium. If required, the gaseous feed may be subjected to one or more pre-treatment procedures to remove impurities and/or unwanted components which could solidify in either of the fractionations.
The gaseous feed is cooled and partially condensed prior to the first fractionation. In order to minimise power consumption, heat exchange during cooling of the gaseous feed may be used to provide reboil to the second fractionation. In addition, cooling of the gaseous feed may be obtained by heat exchange with the hydrocarbon product low in nitrogen from the second fractionation and/or the nitrogen rich stream from the second fractionation. In one preferred embodiment, the hydrocarbon product low in nitrogen from the second fractionation is pumped to elevated pressure and evaporated to provide cooling to the gaseous feed.
The gaseous feed may also be split into at least two streams, each of which may be independently processed according to any of the steps described above before being directed to the first fractionation. Where at least one of the at least two streams is used to provide reboil to the second fractionation energy efficiently via heat exchange, that stream is preferably fed to an intermediate stage of the first fractionation. Where at least one of the at least two streams is not used to provide reboil to the second fractionation, that stream is preferably fed below the bottom stage of the first fractionation to provide stripping vapour. Preferably the first fractionation is at a pressure of 5 to 30 bar (0.5 to 3.0 MPa).
In addition, reboil in the second fractionation may be provided by heat exchange with the overhead vapour stream from the first fractionation during the partial condensation thereof, thereby reducing energy consumption.
In step (iv) of the process described above, the first stream may comprise between 10% and 50% of the sub cooled product.
In a preferred embodiment, the first stream is expanded to form a two-phase feed, prior to being fed to the second fractionation. The second stream is preferably expanded to form a two-phase feed before being reheated via heat exchange with the separated vapour stream from step (iii). If required, further reheating of the second stream, after expansion thereof, may be effected by heat exchange with the condensed product from the first fractionation and/or the overhead vapour stream from the first fractionation.
Preferably the first stream is fed to the second fractionation at a higher stage than the second stream.
The hydrocarbon product stream low in nitrogen from the second fractionation is preferably removed from the second fractionation as a liquid stream.
In a further embodiment, the nitrogen rich stream from the second fractionation may be reheated by heat exchange with the overhead vapour stream from the first fractionation during partial condensation thereof and/or by heat exchange with the separated vapour stream in step (iii) during condensation thereof.
It will be appreciated by the skilled person that the residual nitrogen content of the hydrocarbon product and the residual hydrocarbon content of the nitrogen rich stream obtained from the second fractionation are dependent on the composition of the feed gas. However, the process of the present invention typically provides a hydrocarbon product comprising 2 mol% or less residual nitrogen content, and possibly a hydrocarbon product comprising less than I mol% residual nitrogen can be obtained. However, in other embodiments the process may be operated with a more relaxed specification so as to obtain a hydrocarbon product having, for example, up to 10 mol% residual nitrogen content.
The present invention also provides an apparatus for the separation of nitrogen from a gaseous feed comprising a mixture of hydrocarbons, the apparatus comprising of: (i) means for cooling and at least partially condensing the gaseous feed; (ii) a first fractionator for producing an overhead vapour stream and a condensed product and a second fractionator operable at a lower pressure than the first fractionator; (iii) means for conveying the cooled and at least partially condensed feed from step (i) to the first fractionator; (iv) means for conveying the condensed product from the first fractionator to the second fractionator; (v) means for partially condensing the overhead vapour stream, and means for separating the partially condensed vapour stream to provide a liquid stream, and a vapour stream; (vi) means for conveying the liquid stream to the first fractionator which is used to provide reflux to the first fractionation, and means for conveying and condensing the vapour stream to provide reflux to the second fractionator; (vii) means for dividing the condensed product of the first fractionator, prior to entry into the second fractionator, into at least two streams; (viii) means for expanding a first stream prior to entry into the second fractionator, and means for expanding and heating prior to entry into the second fractionator; (ix) means for conveying a hydrocarbon product low in nitrogen from the second fractionator; and (x) means for conveying a nitrogen rich stream from the second fractionator.
In one embodiment, the first and second fractionators may be in a stacked configuration, with the second fractionator positioned above the first fractionator.
In an alternate embodiment, the overall height of the apparatus may be reduced by arranging the first and second fractionators in a non-stacked configuration.
Preferably, the second fractionator comprises a reboil heat exchanger.
Suitable means for expanding the streams include liquid and two-phase expansion turbines.
The invention will now be described in greater detail with reference to preferred embodiments and with the aid of the accompanying figures, in which: Figure 1 shows a conventional stacked double column apparatus for the separation of nitrogen from a gaseous mixture comprising nitrogen gas and hydrocarbons, as described above.
Figure 2 shows a stacked double column apparatus in accordance with the present invention.
Figure 3 shows an uncoupled double column apparatus also in accordance with the present invention Figure 4 also shows an uncoupled double column apparatus in accordance with the present invention.
In the embodiment of the invention shown in Figure 2, a high pressure column (08) and a low pressure column (15) are provided in a stacked arrangement, with the high pressure column (08) positioned below the low pressure column (15).
A feed gas (01) is cooled and at least partially condensed in a heat exchanger (02) and is expanded across valve (06) to form two-phase feed (07) to the bottom of the high pressure column (08). The high pressure column (08) separates the two-phase feed (07) into a nitrogen rich overhead vapour fraction (19) and a hydrocarbon rich liquid fraction (09) The hydrocarbon rich liquid fraction (09) from the high pressure column (08) is sub-cooled in heat exchanger (10) and the resulting stream (12) Es split into two portions. One portion is expanded across valve (13) to form a two-phase feed stream (14) which is fed to an intermediate stage of the low pressure column (15). The other portion is expanded across valve (16) and is reheated at low pressure to form a two-phase feed stream (18), which has a higher vapour fraction and is fed to a lower stage of the low pressure column (15) than feed stream (14).
The overhead vapour (19) from the high pressure column (08) is partially condensed in heat exchange with boiling liquid at the bottom of the low pressure column (15) in a reboil heat exchanger (04). The boiling liquid may either be piped to the reboil heat exchanger (04) from a bottom tray or packed section of the low pressure column (15), or the reboil heat exchanger (04) may be submerged in the liquid in the sump of the low pressure column (15). -10-
The partially condensed overhead stream (20)is separated into a liquid stream (22) and a separated vapour stream (23) in a phase separator (21). The liquid stream (22) is passed as reflux to the high pressure column (08). The separated vapour stream (23) is fully condensed and sub-cooled in heat exchangers (10) and (24) to form stream (25) which is expanded across valve (26) and is passed as reflux (27) to the low pressure column (15).
A hydrocarbon product (31) with low nitrogen content from the low pressure column (15) is pumped to an elevated pressure by a pump (32), dependent on the composition and pressure of the feed gas (01), and the resulting stream (33) is evaporated and reheated in heat exchangers (10) and (02) to form a gaseous product (35). Evaporation and reheating of the hydrocarbon stream (33) in heat exchanger (02) preferably provides at least a portion of, and more preferably the majority of, the refrigeration required for cooling and condensation of the feed gas (01).
A nitrogen vapour stream (28) with low hydrocarbon content from the low pressure column (15) is preferably reheated in heat exchanger (24) to provide further refrigeration for sub-cooling of the separated vapour stream (23) and is preferably further reheated in heat exchangers (10) and (02).
In the embodiment of the invention shown in Figure 3, a high pressure column (08) and a low pressure column (15) are provided in an uncoupled arrangement.
A feed gas (01) is cooled and at least partially condensed in a heat exchanger (02) and is then sub-cooled in heat exchange with boiling liquid at the bottom of the low pressure column (15) in a reboil heat exchanger (04). The boiling liquid may either be piped to the reboil heat exchanger (04) from a bottom tray or packed section of the low pressure column (15), or the reboil heat exchanger (04) may be submerged in the liquid in the sump of the low pressure column (15). The cooled and at least partially condensed feed gas (05) is expanded across valve (06) to form two-phase feed (07) to the bottom of the high pressure column (08). -11 -
The hydrocarbon rich liquid fraction (09) from the high pressure column (08) is sub-cooled in heat exchangers (10) and (11) and the resulting stream (12) is split into two portions. One portion is expanded across a valve (13) to form a two-phase feed stream (14) to an intermediate stage of the low pressure column (15). The other portion is expanded across a valve (16) and is reheated at low pressure to form a two-phase feed stream (18), which has a higher vapour fraction and is fed to a lower stage of the low pressure column (15) than feed stream (14).
The overhead vapour (19) from the high pressure column (08) is partially condensed in heat exchanger (10). The partially condensed overhead stream (20) is separated into a liquid stream (22) and a separated vapour stream (23) in a phase separator (21). The liquid stream (22) is passed as reflux to the high pressure column (08). The separated vapour stream (23) is fully condensed and sub-cooled in heat exchangers (11) and (24) to form stream (25) which is expanded across a valve (26) and is passed as reflux (27) to the low pressure column (15).
A hydrocarbon product (31) with low nitrogen content, from the low pressure column (15), is pumped to an elevated pressure by a pump (32), dependent on the composition and pressure of the feed gas (01), and the resulting stream (33) is evaporated and reheated in heat exchanger (02) to form a gaseous product (34). Evaporation and reheating of the hydrocarbon stream (33) in the heat exchanger (02) preferably provides at least a portion of, and more preferably the majority of, the refrigeration required for cooling and condensation of the feed gas (01).
A nitrogen vapour stream (28) with low hydrocarbon content from the low pressure column (15) is preferably reheated in heat exchanger (24) to provide further refrigeration for sub-cooling of the separated vapour stream (23) and is preferably further reheated in heat exchangers (10) and (02).
In the embodiment of the invention shown in Figure 4, a high pressure column (08) and a low pressure column (15) are provided in an uncoupled arrangement, and multiple feeds are provided to the high pressure column. -12-
A feed gas (01) is cooled and at least partially condensed in a heat exchanger (02) and is split with a portion being expanded across valve (36) to form a two-phase feed (37) which is fed to the bottom of high pressure column (08). The remaining portion of the feed gas (01) is further cooled in a heat exchanger (35) to form a stream (03) which is then sub-cooled in heat exchange with boiling liquid at the bottom of the low pressure column (15) in a reboil heat exchanger (04). The boiling liquid may either be piped to reboil heat exchanger (04) from a bottom tray or packed section of the low pressure column (15), or the reboil heat exchanger (04) may be submerged in the liquid in the sump of the low pressure column (15). The cooled and at least partially condensed feed gas (05) is expanded across valve (06) to form feed stream (07) which is fed to an intermediate stage of high pressure column (08).
The hydrocarbon rich liquid fraction (09) from the high pressure column (08) is sub-cooled in heat exchangers (10) and (11) and the resulting stream (12) is split into two portions. One portion is expanded across valve (13) to form a two-phase feed stream (14) which is fed to an intermediate stage of a low pressure column (15). The other portion is expanded across valve (16) and is reheated at low pressure to form a two-phase feed stream (18) which has a higher vapour fraction and is fed to a lower stage of the low pressure column (15) than feed stream (14).
The overhead vapour (19) from the high pressure column is partially condensed in a heat exchanger (10). The partially condensed overhead stream (20) is separated into a liquid stream (22) and a separated vapour portion (23) in a phase separator (21). The liquid stream (22) passes as reflux to the high pressure column (08). The separated vapour stream (23) is fully condensed and subcooled in heat exchangers (11) and (24) to form a stream (25) which is expanded across valve (26) and is passed as reflux (27) to the low pressure column (15).
A hydrocarbon product (31) with low nitrogen content, from the low pressure column (15), is pumped to an elevated pressure by pump (32), dependent on the composition and pressure of feed gas (01), and the resulting stream (33) is evaporated and reheated in -13-heat exchangers (35) and (02) to form a gaseous product (34). Evaporation and reheating of the hydrocarbon stream (33) in the heat exchangers (35) and (02) preferably provides at least a portion of, and more preferably the majority of, the refrigeration required for cooling and condensation of the feed gas (01).
A nitrogen vapour stream (28) with low hydrocarbon content from the low pressure column (15) is preferably reheated in heat exchanger (24) to provide further refrigeration for sub-cooling of the separated vapour stream (23) and is preferably further reheated in heat exchangers (11), (10), (35) and (02).
ExamDles Comparative Example 1 Table I shows typical operating parameters for the conventional double column apparatus shown in Figure 1 when used to separate a gaseous mixture consisting of 40 mol% nitrogen gas and 60 mol% methane. It will be observed that, based on 6 theoretical separation stages in the high pressure column (08) and 6 theoretical separation stages in the low pressure column (15), the conventional double column apparatus is able to separate such a mixture to obtain a nitrogen product stream (Stream 30) having a residual methane content of 0.8 mol% when producing a methane product stream (Stream 35) having a residual nitrogen content of 2.0 mol%.
Table I
Stream1 1 7 9 14 19 22 23 Pressure2 MPa 3.00 2.70 2.70 0.22 2.68 2.68 2.68 Temperature °C 35.0 -127.6 -127.7 -171.2 -146.4 -149.6 -149.6 Mass Flow kg/h 104155 104155 84014 84014 53792 33651 20140 Molar Flow mol/h 5000.0 5000.0 4255.5 4255.5 1988.2 1243.8 744.4 Nitrogen mol % 40.0 40.0 30.9 30.9 92.0 92.0 92.0 Methane mol% 60.0 60.0 69.1 69.1 8.0 8.0 8. 0 -14-Stream1 27 28 30 31 35 Pressure2 MPa 0.22 0.20 0.15 0.22 0.98 Temperature °C -187.7 -188.3 28.5 -155.9 28.5 Mass Flow kg/h 20140 54562 54562 49592 49592 Molar Flow mol/h 744.4 1954.4 1954.4 3045.6 3045.6 Nitrogen mol% 92.0 99.2 99.2 2.0 2.0 Methane mol% 8.0 0.8 0.8 98.0 98.0 1As identified in Figure 1 2Pressures are given as absolute values Comparative Example 2 Table 2 shows typical operating parameters for the conventional double column apparatus shown in Figure 1 when used to separate a gaseous mixture consisting of 30 mol% nitrogen gas and 70 mol% methane. It will be observed that, based on the same number of theoretical separation stages in columns (08) and (15) as per Comparative Example 1, and producing a methane product stream (Stream 35) having a residual nitrogen content of 2.0 mol%, hydrocarbon recovery in the conventional double column apparatus is reduced, with the residual methane content of the nitrogen product stream (Stream 30) increasing to 11.lmol%.
Table 2
Stream1 1 7 9 14 19 22 23 Pressure2 MPa 3.00 2.70 2.70 0.22 2.68 2.68 2.68 Temperature °C 35.0 -122.5 -122.6 -167.7 -147.1 -149.9 -149.9 Mass Flow kg/h 98170 98170 85562 85562 45074 32466 12608 Molar Flow mol/h 5000.0 5000.0 4536.0 1536.0 1658.6 1194.6 464.0 Nitrogen mol% 30.0 30.0 23.6 69.6 93.0 93.0 93.0 Methane mol% 70.0 70.0 76.4 30.4 7.0 7.0 7.0 Stream1 27 28 30 31 35 Pressure2 MPa 0.22 0.20 0.15 0.22 0.12 Temperature °C -187.7 -176.4 29.3 -155.9 29.3 Mass Flow kg/h 12608 42981 42981 55188 55188 Molar Flow mol/h 464.0 1610.5 1610.5 3389.5 3389.5 Nitrogen mol% 93.0 88.9 88.9 2.0 2.0 Methane mol% 7.0 11.1 11.1 98.0 98.0 As identified in Figure 1 2Pressures are given as absolute values
Example 3
Table 3 shows typical operating parameters for the process of the invention using the apparatus shown in Figure 2, when used to separate a gaseous mixture consisting of 40 mol% nitrogen gas and 60 mol% methane. With this gaseous mixture, the first stream accounts for 33% by molar flow of the sub cooled product. It will be observed that, based on the same number of theoretical separation stages in columns (08) and (15) as per Comparative Example 1, the process of the invention is able to separate such a mixture to obtain a nitrogen product stream (Stream 30) having an improved residual methane content of 0.4 mol% when producing a methane product stream (Stream 35) having a residual nitrogen content of 2.0 mol%.
Table 3
Stream1 1 7 9 14 18 19 22 Pressure2 MPa 3.00 2.50 2.50 0.22 0.22 2.48 2.48 Temperature °C 35.0 -129.8 -129.9 -178.9 -158.2 -149.1 -151.3 Mass Flow kg/h 104155 104155 84366 56508 27858 53384 33596 Molar Flow mol/h 5000.0 5000.0 4284.0 2869.4 1414.6 1957.7 1241.7 Nitrogen mol% 40.0 40.0 30.5 30.5 30.5 93.8 92.0 Methane mol% 60.0 60.0 69.5 69.5 69.5 6.2 8.0 -16-Stream1 23 27 28 30 31 35 Pressure2 MPa 2.48 0.22 0.20 0.15 0.22 0.98 Temperature °C -151.3 -188.2 -188.9 28.5 -155.9 28.5 Mass Flow kg/h 19789 19789 54443 54443 49712 49712 Molar Flow mol/h 716.0 716.0 1946.7 1946.7 3053.3 3053 Nitrogen mol% 96.9 96.9 99.6 99.6 2.0 2.0 Methane mol% 3.1 3.1 0.4 0.4 98.0 98.0 1As identified in Figure 2 2Pressures are given as absolute values
Example 4
Table 4 shows typical operating parameters for the process of the invention using the apparatus shown in Figure 2, when used to separate a gaseous mixture consisting of 30 mol% nitrogen gas and 70 mol% methane. In contrast with the conventional double column apparatus shown in Figure 1, the process and apparatus of the invention is able to maintain good separation efficiency even when the nitrogen content of the gaseous feed is below 35 mol%. With this gaseous mixture, the first stream accounts for 25% by molar flow of the sub cooled product. Thus, using the process and apparatus of the invention, based on the same number of theoretical separation stages in columns (08) and (15) as per Comparative Example 2, it is possible to obtain a nitrogen product stream (Stream 30) having a residual methane content of 1.0 mol% (compared with 11.1 mol% in Comparative Example 2), when producing a methane product stream (Stream 35) having a residual nitrogen content of 2.0 mol%.
Table 4
Stream1 1 7 9 14 18 19 22 Pressure2 MPa 3.00 2.00 2.00 0.22 0.22 1.98 1.98 Temperature °C 35.0 -131.7 -131.7 -175.6 -156.3 -146.9 -153.2 Mass Flow kg/h 98170 98170 84871 63762 21109 28263 14964 Molar Flow mol/h 5000.0 5000.0 4513.1 3390.7 1122.5 1071.0 584.1 Nitrogen mol% 30.0 30.0 23.1 23.1 23.1 86.4 80.0 Methane mol% 70.0 70.0 76.9 76.9 76.9 13.6 20.0 Stream1 23 27 28 30 31 35 Pressure2 MPa 1.98 0.22 0.20 0.15 0.22 1.18 Temperature °C -153.2 -187.9 -188.0 29.3 -155.9 29.3 Mass Flow kg/h 13299 13299 40267 40267 57903 57903 Molar Flow mol/h 486.9 486.9 1443.7 1443.7 3556.3 3556.3 Nitrogen mol% 94.2 94.2 99.0 99.0 2.0 2.0 Methane mol% 5.8 5.8 1.0 1.0 98.0 98.0 1As identified in Figure 2 2Pressures are given as absolute values -18- Process and Apparatus for Separation of Hydrocarbons and Nitrogen This invention relates to processes and apparatus for the low temperature separation of nitrogen from a gaseous mixture comprising nitrogen gas and hydrocarbons. Such mixtures occur naturally in geological formations and can also result from nitrogen injection as a method of improving oil or gas production. Nitrogen separation may be required as part of an overall processing of gaseous hydrocarbons to meet sales specifications, such as maximum inert content or minimum calorific value.
Low temperature fractionation presents an energy efficient method for the separation of nitrogen from gaseous hydrocarbon streams, in particular gaseous hydrocarbon streams wherein the hydrocarbons comprise predominantly methane, such as natural gas.
Separated nitrogen streams of high purity can be produced, thereby maximising hydrocarbon recovery and, where the nitrogen stream is vented to atmosphere, minimising environmental impact.
Where the nitrogen content is higher than approximately 35 to 40 mol%, a double column arrangement (such as disclosed in US 7,127,915) similar to that used in air separation is conventional and is often the most economical choice considering both capital cost and energy consumption. The columns are typically configured in a stacked arrangement, with the upper fractionation column operating at low pressure, just above atmospheric, and the lower fractionation column operating at high pressure, typically at approximately 27 bar (2700 kPa).
An example of a conventional double column arrangement is shown in Figure 1.
A feed gas (01) is cooled and at least partially condensed in heat exchanger (02). The partially condensed feed (03) is expanded across valve (06) to form a two-phase feed (07) which is fed to a high pressure column (08). The high pressure column (08) separates the two-phase feed (07) into a nitrogen rich overhead vapour fraction (19) and a hydrocarbon rich liquid fraction (09).
The hydrocarbon rich liquid fraction (09) from the high pressure column (08) is sub-cooled in heat exchanger (10) to form stream (12) which is expanded across valve (13) to form a further two-phase feed stream (14) which is fed to an intermediate stage of a low pressure column (15).
The overhead vapour (19) from the high pressure column (08) is fully condensed in heat exchange with boiling liquid at the bottom of the low pressure column (15) in reboil heat exchanger (04). The liquid may either be piped from the bottom tray or packed section, or the reboil heat exchanger (04) may be submerged in the liquid in the sump of the low pressure column (15).
The fully condensed overhead stream (20) is split. A portion is passed as reflux (22) to the high pressure column (08) and a portion (23) is sub-cooled in heat exchangers (10) and (24) to form stream (25) which is expanded across valve (26) and passes as reflux (27) to the low pressure column (15).
A hydrocarbon product (31) with low nitrogen content, from the low pressure column (15), is pumped to an elevated pressure, dependent on the composition and pressure of feed gas (01), and is rewarmed and evaporated in heat exchangers (10) and (02) to form a gaseous product (35), providing the majority of the refrigeration for cooling and condensation of the feed gas (01).
A nitrogen vapour stream (28) with low methane content from the low pressure column (15) is rewarmed in heat exchanger (24) to provide refrigeration for sub-cooling of the nitrogen rich reflux stream and is further rewarmed in heat exchangers (10) and (02).
The purity of the hydrocarbon product (31) from the bottom of the low pressure fractionation column (15) is ensured by provision of sufficient reboil in heat exchange with the overhead vapour from the high pressure column (08) in the reboil heat exchanger (04). Purity of the nitrogen product from the low pressure fractionation column overhead (28) is ensured by conditioning the feed streams to the column and, in particular, providing sufficient flow of nitrogen rich reflux (27).
The pressure drop between high pressure fractionation column (08) and low pressure fractionation column (15) provides the required refrigeration by Joule-Thomson expansion. High purity nitrogen and hydrocarbon streams are withdrawn from the top and bottom of the low pressure fractionation column (15) respectively.
When the nitrogen content of the feed gas to a conventional double column system is lower than approximately 35 mol%, insufficient reflux is normally generated to the low pressure fractionation column to maintain low losses of hydrocarbons with the nitrogen product.
In such cases, options to increase the available reflux include: a) compressing the reject nitrogen stream and recycling it to the feed gas or other part of the process to meet reflux requirements; and b) introducing an upstream pre-separation' system to condition the feed gas to produce a stream suitably enriched in nitrogen to feed to the double column system.
Process selection will be dependent on considerations such as plant capacity, feed gas nitrogen content and variability and feed and product gas pressure. Use of an upstream pre-separation' system is efficient in producing product gas at elevated pressure, hence reducing product gas compression power requirements and may also be preferred when the gaseous feed comprises contaminants such as carbon dioxide and heavy hydrocarbons, which are tolerated at higher levels in the pre-separation system. Inclusion of either a pre-separation system or a nitrogen recycle system does however introduce additional equipment items.
The present invention provides an alternative double column system for the separation of nitrogen from a gaseous mixture comprising nitrogen gas and hydrocarbons which uses improved heat integration to maximise the nitrogen reflux stream and to optimise the feed conditions to the low pressure fractionation column. This provides additional flexibility to process gases having low nitrogen content, for example less than 35 mol%, and potentially as low as 20 mol% without recourse to the use of additional equipment for pre-separation or nitrogen recycling as described above. However, the invention is also useful for the separation of gases having nitrogen content above 35 mol%, with improved separation efficiency being observed in comparison with conventional separation techniques.
The present invention provides a process for the separation of nitrogen from a gaseous feed comprising a mixture of hydrocarbons and nitrogen gas, the process comprising the steps of: (I) cooling and at least partially condensing the gaseous feed; (ii) feeding the cooled and at least partially condensed feed from step (i) to a first fractionation to produce an overhead vapour stream having an enriched nitrogen content and a condensed product having a reduced nitrogen content which is subjected to a second fractionation, which comprises reboil, at a lower pressure than the first fractionation; (iii) partially condensing the overhead vapour stream, and separating to provide a liquid stream, which is used to provide reflux to the first fractionation, and a separated vapour stream, which is condensed to provide reflux to the second fractionation; and (iv) sub-cooling the condensed product of the first fractionation and dividing the resulting sub-cooled product into at least two streams: a first stream being expanded and fed to the second fractionation, and a second stream being expanded and reheated in heat exchange with the separated vapour stream from step (iii) before being fed to the second fractionation; (v) removing a hydrocarbon product stream low in nitrogen from the second fractionation; and (vi) removing a nitrogen rich stream from the second fractionation.
The combination of steps (iii) and (iv) enables separation of feed streams with lower nitrogen content than is feasible with prior art processes, such as the conventional double column arrangement described above.
In particular, partial condensation of the overhead vapour stream from the first fractionation allows the separated vapour stream from step (iii) to be efficiently condensed in heat exchange with reheat of the second stream of the condensed product in step (iv) to provide reflux to the second fractionation. The reheated second stream has an increased vapour fraction and its introduction into the second fractionation provides an increased quantity of stripping vapour to the second fractionation. For a given feed composition, the effect of these steps is to provide improved separation, even for feed compositions comprising less than 35 mol% nitrogen, for example 20 to 35 mol%, while maintaining the overall energy efficiency of the separation process.
As a further advantage, partial condensation of the overhead stream from the first fractionation allows the first fractionation and the second fractionation steps to be decoupled' as there is no physical requirement for the second fractionator to be elevated above the first fractionator.
In a preferred embodiment, the hydrocarbons in the gaseous feed comprise or consist of methane. For instance, the gaseous feed may comprise or consist of natural gas. In further preferred embodiments, the gaseous feed comprises less than 40 mol% nitrogen, less than 35 mol% nitrogen, or less than 30 mol% nitrogen. Preferably, the gaseous feed comprises at least 20 mol% nitrogen. The gaseous feed may further comprise other inert gases, such as helium. If required, the gaseous feed may be subjected to one or more pre-treatment procedures to remove impurities and/or unwanted components which could solidify in either of the fractionations.
The gaseous feed is cooled and partially condensed prior to the first fractionation. In order to minimise power consumption, heat exchange during cooling of the gaseous feed may be used to provide reboil to the second fractionation. In addition, cooling of the gaseous feed may be obtained by heat exchange with the hydrocarbon product low in nitrogen from the second fractionation and/or the nitrogen rich stream from the second fractionation. In one preferred embodiment, the hydrocarbon product low in nitrogen from the second fractionation is pumped to elevated pressure and evaporated to provide cooling to the gaseous feed.
The gaseous feed may also be split into at least two streams, each of which may be independently processed according to any of the steps described above before being directed to the first fractionation. Where at least one of the at least two streams is used to provide reboil to the second fractionation energy efficiently via heat exchange, that stream is preferably fed to an intermediate stage of the first fractionation. Where at least one of the at least two streams is not used to provide reboil to the second fractionation, that stream is preferably fed below the bottom stage of the first fractionation to provide stripping vapour. Preferably the first fractionation is at a pressure of 5 to 30 bar (0.5 to 3.0 MPa).
In addition, reboil in the second fractionation may be provided by heat exchange with the overhead vapour stream from the first fractionation during the partial condensation thereof, thereby reducing energy consumption.
In step (iv) of the process described above, the first stream may comprise between 10% and 50% of the sub cooled product.
In a preferred embodiment, the first stream is expanded to form a two-phase feed, prior to being fed to the second fractionation. The second stream is preferably expanded to form a two-phase feed before being reheated via heat exchange with the separated vapour stream from step (iii). If required, further reheating of the second stream, after expansion thereof, may be effected by heat exchange with the condensed product from the first fractionation and/or the overhead vapour stream from the first fractionation.
Preferably the first stream is fed to the second fractionation at a higher stage than the second stream.
The hydrocarbon product stream low in nitrogen from the second fractionation is preferably removed from the second fractionation as a liquid stream.
In a further embodiment, the nitrogen rich stream from the second fractionation may be reheated by heat exchange with the overhead vapour stream from the first fractionation during partial condensation thereof and/or by heat exchange with the separated vapour stream in step (iii) during condensation thereof.
It will be appreciated by the skilled person that the residual nitrogen content of the hydrocarbon product and the residual hydrocarbon content of the nitrogen rich stream obtained from the second fractionation are dependent on the composition of the feed gas. However, the process of the present invention typically provides a hydrocarbon product comprising 2 mol% or less residual nitrogen content, and possibly a hydrocarbon product comprising less than I mol% residual nitrogen can be obtained. However, in other embodiments the process may be operated with a more relaxed specification so as to obtain a hydrocarbon product having, for example, up to 10 mol% residual nitrogen content.
The present invention also provides an apparatus for the separation of nitrogen from a gaseous feed comprising a mixture of hydrocarbons, the apparatus comprising of: (i) means for cooling and at least partially condensing the gaseous feed; (ii) a first fractionator for producing an overhead vapour stream and a condensed product and a second fractionator operable at a lower pressure than the first fractionator; (iii) means for conveying the cooled and at least partially condensed feed from step (i) to the first fractionator; (iv) means for conveying the condensed product from the first fractionator to the second fractionator; (v) means for partially condensing the overhead vapour stream, and means for separating the partially condensed vapour stream to provide a liquid stream, and a vapour stream; (vi) means for conveying the liquid stream to the first fractionator which is used to provide reflux to the first fractionation, and means for conveying and condensing the vapour stream to provide reflux to the second fractionator; (vii) means for dividing the condensed product of the first fractionator, prior to entry into the second fractionator, into at least two streams; (viii) means for expanding a first stream prior to entry into the second fractionator, and means for expanding and heating prior to entry into the second fractionator; (ix) means for conveying a hydrocarbon product low in nitrogen from the second fractionator; and (x) means for conveying a nitrogen rich stream from the second fractionator.
In one embodiment, the first and second fractionators may be in a stacked configuration, with the second fractionator positioned above the first fractionator.
In an alternate embodiment, the overall height of the apparatus may be reduced by arranging the first and second fractionators in a non-stacked configuration.
Preferably, the second fractionator comprises a reboil heat exchanger.
Suitable means for expanding the streams include liquid and two-phase expansion turbines.
The invention will now be described in greater detail with reference to preferred embodiments and with the aid of the accompanying figures, in which: Figure 1 shows a conventional stacked double column apparatus for the separation of nitrogen from a gaseous mixture comprising nitrogen gas and hydrocarbons, as described above.
Figure 2 shows a stacked double column apparatus in accordance with the present invention.
Figure 3 shows an uncoupled double column apparatus also in accordance with the present invention Figure 4 also shows an uncoupled double column apparatus in accordance with the present invention.
In the embodiment of the invention shown in Figure 2, a high pressure column (08) and a low pressure column (15) are provided in a stacked arrangement, with the high pressure column (08) positioned below the low pressure column (15).
A feed gas (01) is cooled and at least partially condensed in a heat exchanger (02) and is expanded across valve (06) to form two-phase feed (07) to the bottom of the high pressure column (08). The high pressure column (08) separates the two-phase feed (07) into a nitrogen rich overhead vapour fraction (19) and a hydrocarbon rich liquid fraction (09) The hydrocarbon rich liquid fraction (09) from the high pressure column (08) is sub-cooled in heat exchanger (10) and the resulting stream (12) Es split into two portions. One portion is expanded across valve (13) to form a two-phase feed stream (14) which is fed to an intermediate stage of the low pressure column (15). The other portion is expanded across valve (16) and is reheated at low pressure to form a two-phase feed stream (18), which has a higher vapour fraction and is fed to a lower stage of the low pressure column (15) than feed stream (14).
The overhead vapour (19) from the high pressure column (08) is partially condensed in heat exchange with boiling liquid at the bottom of the low pressure column (15) in a reboil heat exchanger (04). The boiling liquid may either be piped to the reboil heat exchanger (04) from a bottom tray or packed section of the low pressure column (15), or the reboil heat exchanger (04) may be submerged in the liquid in the sump of the low pressure column (15). -10-
The partially condensed overhead stream (20)is separated into a liquid stream (22) and a separated vapour stream (23) in a phase separator (21). The liquid stream (22) is passed as reflux to the high pressure column (08). The separated vapour stream (23) is fully condensed and sub-cooled in heat exchangers (10) and (24) to form stream (25) which is expanded across valve (26) and is passed as reflux (27) to the low pressure column (15).
A hydrocarbon product (31) with low nitrogen content from the low pressure column (15) is pumped to an elevated pressure by a pump (32), dependent on the composition and pressure of the feed gas (01), and the resulting stream (33) is evaporated and reheated in heat exchangers (10) and (02) to form a gaseous product (35). Evaporation and reheating of the hydrocarbon stream (33) in heat exchanger (02) preferably provides at least a portion of, and more preferably the majority of, the refrigeration required for cooling and condensation of the feed gas (01).
A nitrogen vapour stream (28) with low hydrocarbon content from the low pressure column (15) is preferably reheated in heat exchanger (24) to provide further refrigeration for sub-cooling of the separated vapour stream (23) and is preferably further reheated in heat exchangers (10) and (02).
In the embodiment of the invention shown in Figure 3, a high pressure column (08) and a low pressure column (15) are provided in an uncoupled arrangement.
A feed gas (01) is cooled and at least partially condensed in a heat exchanger (02) and is then sub-cooled in heat exchange with boiling liquid at the bottom of the low pressure column (15) in a reboil heat exchanger (04). The boiling liquid may either be piped to the reboil heat exchanger (04) from a bottom tray or packed section of the low pressure column (15), or the reboil heat exchanger (04) may be submerged in the liquid in the sump of the low pressure column (15). The cooled and at least partially condensed feed gas (05) is expanded across valve (06) to form two-phase feed (07) to the bottom of the high pressure column (08). -11 -
The hydrocarbon rich liquid fraction (09) from the high pressure column (08) is sub-cooled in heat exchangers (10) and (11) and the resulting stream (12) is split into two portions. One portion is expanded across a valve (13) to form a two-phase feed stream (14) to an intermediate stage of the low pressure column (15). The other portion is expanded across a valve (16) and is reheated at low pressure to form a two-phase feed stream (18), which has a higher vapour fraction and is fed to a lower stage of the low pressure column (15) than feed stream (14).
The overhead vapour (19) from the high pressure column (08) is partially condensed in heat exchanger (10). The partially condensed overhead stream (20) is separated into a liquid stream (22) and a separated vapour stream (23) in a phase separator (21). The liquid stream (22) is passed as reflux to the high pressure column (08). The separated vapour stream (23) is fully condensed and sub-cooled in heat exchangers (11) and (24) to form stream (25) which is expanded across a valve (26) and is passed as reflux (27) to the low pressure column (15).
A hydrocarbon product (31) with low nitrogen content, from the low pressure column (15), is pumped to an elevated pressure by a pump (32), dependent on the composition and pressure of the feed gas (01), and the resulting stream (33) is evaporated and reheated in heat exchanger (02) to form a gaseous product (34). Evaporation and reheating of the hydrocarbon stream (33) in the heat exchanger (02) preferably provides at least a portion of, and more preferably the majority of, the refrigeration required for cooling and condensation of the feed gas (01).
A nitrogen vapour stream (28) with low hydrocarbon content from the low pressure column (15) is preferably reheated in heat exchanger (24) to provide further refrigeration for sub-cooling of the separated vapour stream (23) and is preferably further reheated in heat exchangers (10) and (02).
In the embodiment of the invention shown in Figure 4, a high pressure column (08) and a low pressure column (15) are provided in an uncoupled arrangement, and multiple feeds are provided to the high pressure column. -12-
A feed gas (01) is cooled and at least partially condensed in a heat exchanger (02) and is split with a portion being expanded across valve (36) to form a two-phase feed (37) which is fed to the bottom of high pressure column (08). The remaining portion of the feed gas (01) is further cooled in a heat exchanger (35) to form a stream (03) which is then sub-cooled in heat exchange with boiling liquid at the bottom of the low pressure column (15) in a reboil heat exchanger (04). The boiling liquid may either be piped to reboil heat exchanger (04) from a bottom tray or packed section of the low pressure column (15), or the reboil heat exchanger (04) may be submerged in the liquid in the sump of the low pressure column (15). The cooled and at least partially condensed feed gas (05) is expanded across valve (06) to form feed stream (07) which is fed to an intermediate stage of high pressure column (08).
The hydrocarbon rich liquid fraction (09) from the high pressure column (08) is sub-cooled in heat exchangers (10) and (11) and the resulting stream (12) is split into two portions. One portion is expanded across valve (13) to form a two-phase feed stream (14) which is fed to an intermediate stage of a low pressure column (15). The other portion is expanded across valve (16) and is reheated at low pressure to form a two-phase feed stream (18) which has a higher vapour fraction and is fed to a lower stage of the low pressure column (15) than feed stream (14).
The overhead vapour (19) from the high pressure column is partially condensed in a heat exchanger (10). The partially condensed overhead stream (20) is separated into a liquid stream (22) and a separated vapour portion (23) in a phase separator (21). The liquid stream (22) passes as reflux to the high pressure column (08). The separated vapour stream (23) is fully condensed and subcooled in heat exchangers (11) and (24) to form a stream (25) which is expanded across valve (26) and is passed as reflux (27) to the low pressure column (15).
A hydrocarbon product (31) with low nitrogen content, from the low pressure column (15), is pumped to an elevated pressure by pump (32), dependent on the composition and pressure of feed gas (01), and the resulting stream (33) is evaporated and reheated in -13-heat exchangers (35) and (02) to form a gaseous product (34). Evaporation and reheating of the hydrocarbon stream (33) in the heat exchangers (35) and (02) preferably provides at least a portion of, and more preferably the majority of, the refrigeration required for cooling and condensation of the feed gas (01).
A nitrogen vapour stream (28) with low hydrocarbon content from the low pressure column (15) is preferably reheated in heat exchanger (24) to provide further refrigeration for sub-cooling of the separated vapour stream (23) and is preferably further reheated in heat exchangers (11), (10), (35) and (02).
ExamDles Comparative Example 1 Table I shows typical operating parameters for the conventional double column apparatus shown in Figure 1 when used to separate a gaseous mixture consisting of 40 mol% nitrogen gas and 60 mol% methane. It will be observed that, based on 6 theoretical separation stages in the high pressure column (08) and 6 theoretical separation stages in the low pressure column (15), the conventional double column apparatus is able to separate such a mixture to obtain a nitrogen product stream (Stream 30) having a residual methane content of 0.8 mol% when producing a methane product stream (Stream 35) having a residual nitrogen content of 2.0 mol%.
Table I
Stream1 1 7 9 14 19 22 23 Pressure2 MPa 3.00 2.70 2.70 0.22 2.68 2.68 2.68 Temperature °C 35.0 -127.6 -127.7 -171.2 -146.4 -149.6 -149.6 Mass Flow kg/h 104155 104155 84014 84014 53792 33651 20140 Molar Flow mol/h 5000.0 5000.0 4255.5 4255.5 1988.2 1243.8 744.4 Nitrogen mol % 40.0 40.0 30.9 30.9 92.0 92.0 92.0 Methane mol% 60.0 60.0 69.1 69.1 8.0 8.0 8. 0 -14-Stream1 27 28 30 31 35 Pressure2 MPa 0.22 0.20 0.15 0.22 0.98 Temperature °C -187.7 -188.3 28.5 -155.9 28.5 Mass Flow kg/h 20140 54562 54562 49592 49592 Molar Flow mol/h 744.4 1954.4 1954.4 3045.6 3045.6 Nitrogen mol% 92.0 99.2 99.2 2.0 2.0 Methane mol% 8.0 0.8 0.8 98.0 98.0 1As identified in Figure 1 2Pressures are given as absolute values Comparative Example 2 Table 2 shows typical operating parameters for the conventional double column apparatus shown in Figure 1 when used to separate a gaseous mixture consisting of 30 mol% nitrogen gas and 70 mol% methane. It will be observed that, based on the same number of theoretical separation stages in columns (08) and (15) as per Comparative Example 1, and producing a methane product stream (Stream 35) having a residual nitrogen content of 2.0 mol%, hydrocarbon recovery in the conventional double column apparatus is reduced, with the residual methane content of the nitrogen product stream (Stream 30) increasing to 11.lmol%.
Table 2
Stream1 1 7 9 14 19 22 23 Pressure2 MPa 3.00 2.70 2.70 0.22 2.68 2.68 2.68 Temperature °C 35.0 -122.5 -122.6 -167.7 -147.1 -149.9 -149.9 Mass Flow kg/h 98170 98170 85562 85562 45074 32466 12608 Molar Flow mol/h 5000.0 5000.0 4536.0 1536.0 1658.6 1194.6 464.0 Nitrogen mol% 30.0 30.0 23.6 69.6 93.0 93.0 93.0 Methane mol% 70.0 70.0 76.4 30.4 7.0 7.0 7.0 Stream1 27 28 30 31 35 Pressure2 MPa 0.22 0.20 0.15 0.22 0.12 Temperature °C -187.7 -176.4 29.3 -155.9 29.3 Mass Flow kg/h 12608 42981 42981 55188 55188 Molar Flow mol/h 464.0 1610.5 1610.5 3389.5 3389.5 Nitrogen mol% 93.0 88.9 88.9 2.0 2.0 Methane mol% 7.0 11.1 11.1 98.0 98.0 As identified in Figure 1 2Pressures are given as absolute values
Example 3
Table 3 shows typical operating parameters for the process of the invention using the apparatus shown in Figure 2, when used to separate a gaseous mixture consisting of 40 mol% nitrogen gas and 60 mol% methane. With this gaseous mixture, the first stream accounts for 33% by molar flow of the sub cooled product. It will be observed that, based on the same number of theoretical separation stages in columns (08) and (15) as per Comparative Example 1, the process of the invention is able to separate such a mixture to obtain a nitrogen product stream (Stream 30) having an improved residual methane content of 0.4 mol% when producing a methane product stream (Stream 35) having a residual nitrogen content of 2.0 mol%.
Table 3
Stream1 1 7 9 14 18 19 22 Pressure2 MPa 3.00 2.50 2.50 0.22 0.22 2.48 2.48 Temperature °C 35.0 -129.8 -129.9 -178.9 -158.2 -149.1 -151.3 Mass Flow kg/h 104155 104155 84366 56508 27858 53384 33596 Molar Flow mol/h 5000.0 5000.0 4284.0 2869.4 1414.6 1957.7 1241.7 Nitrogen mol% 40.0 40.0 30.5 30.5 30.5 93.8 92.0 Methane mol% 60.0 60.0 69.5 69.5 69.5 6.2 8.0 -16-Stream1 23 27 28 30 31 35 Pressure2 MPa 2.48 0.22 0.20 0.15 0.22 0.98 Temperature °C -151.3 -188.2 -188.9 28.5 -155.9 28.5 Mass Flow kg/h 19789 19789 54443 54443 49712 49712 Molar Flow mol/h 716.0 716.0 1946.7 1946.7 3053.3 3053 Nitrogen mol% 96.9 96.9 99.6 99.6 2.0 2.0 Methane mol% 3.1 3.1 0.4 0.4 98.0 98.0 1As identified in Figure 2 2Pressures are given as absolute values
Example 4
Table 4 shows typical operating parameters for the process of the invention using the apparatus shown in Figure 2, when used to separate a gaseous mixture consisting of 30 mol% nitrogen gas and 70 mol% methane. In contrast with the conventional double column apparatus shown in Figure 1, the process and apparatus of the invention is able to maintain good separation efficiency even when the nitrogen content of the gaseous feed is below 35 mol%. With this gaseous mixture, the first stream accounts for 25% by molar flow of the sub cooled product. Thus, using the process and apparatus of the invention, based on the same number of theoretical separation stages in columns (08) and (15) as per Comparative Example 2, it is possible to obtain a nitrogen product stream (Stream 30) having a residual methane content of 1.0 mol% (compared with 11.1 mol% in Comparative Example 2), when producing a methane product stream (Stream 35) having a residual nitrogen content of 2.0 mol%.
Table 4
Stream1 1 7 9 14 18 19 22 Pressure2 MPa 3.00 2.00 2.00 0.22 0.22 1.98 1.98 Temperature °C 35.0 -131.7 -131.7 -175.6 -156.3 -146.9 -153.2 Mass Flow kg/h 98170 98170 84871 63762 21109 28263 14964 Molar Flow mol/h 5000.0 5000.0 4513.1 3390.7 1122.5 1071.0 584.1 Nitrogen mol% 30.0 30.0 23.1 23.1 23.1 86.4 80.0 Methane mol% 70.0 70.0 76.9 76.9 76.9 13.6 20.0 Stream1 23 27 28 30 31 35 Pressure2 MPa 1.98 0.22 0.20 0.15 0.22 1.18 Temperature °C -153.2 -187.9 -188.0 29.3 -155.9 29.3 Mass Flow kg/h 13299 13299 40267 40267 57903 57903 Molar Flow mol/h 486.9 486.9 1443.7 1443.7 3556.3 3556.3 Nitrogen mol% 94.2 94.2 99.0 99.0 2.0 2.0 Methane mol% 5.8 5.8 1.0 1.0 98.0 98.0 1As identified in Figure 2 2Pressures are given as absolute values -18-

Claims (34)

1. A process for the separation of nitrogen from a gaseous feed comprising a mixture of hydrocarbons and nitrogen gas, the process comprising the steps of: (i) cooling and at least partially condensing the gaseous feed; (ii) feeding the cooled and at least partially condensed feed from step (i) to a first fractionation to produce an overhead vapour stream having an enriched nitrogen content and a condensed product having a reduced nitrogen content which is subjected to a second fractionation, which comprises reboil, at a lower pressure than the first fractionation; (iii) partially condensing the overhead vapour stream, and separating to provide a liquid stream, which is used to provide reflux to the first fractionation, and a separated vapour stream, which is condensed to provide reflux to the second fractionation; and (iv) sub-cooling the condensed product of the first fractionation and dividing the resulting sub-cooled product into at least two streams: a first stream being expanded and fed to the second fractionation, and a second stream being expanded and reheated in heat exchange with the separated vapour stream from step (ii) before being fed to the second fractionation; (v) removing a hydrocarbon product stream low in nitrogen from the second fractionation; and (vi) removing a nitrogen rich stream from the second fractionation.
2. A process according to Claim 1, wherein the hydrocarbons in the gaseous feed comprise or consist of methane.
3. A process according to Claim I of Claim 2, wherein the gaseous feed comprises or consists of natural gas.
4. A process according to any one of the preceding claims, wherein the gaseous feed comprises less than 40 mol% nitrogen.
5. A process according to Claim 4, wherein the gaseous feed comprises less than 35 mol% nitrogen.
6. A process according to Claim 5, wherein the gaseous feed comprises less than mol% nitrogen.
7. A process according to any one of the preceding claims, wherein the gaseous feed comprises at least 20 mol% nitrogen.
8. A process according to any one of the preceding claims, wherein reboil in the second fractionation is provided at least in part by heat exchange during cooling of the gaseous feed.
9. A process according to any one of the preceding claims, wherein the gaseous feed is cooled and at least partially condensed via heat exchange with the hydrocarbon product stream low in nitrogen from the second fractionation and/or the nitrogen rich stream from the second fractionation.
10.A process according to Claim 9, wherein the hydrocarbon product stream low in nitrogen is pumped to elevated pressure and evaporated to provide cooling for the gaseous feed.
11.A process according to any one of the preceding claims, wherein the gaseous feed is expanded prior to the first fractionation.
12.A process according to any one of the preceding claims, wherein the gaseous feed is split into at least two streams, and each stream is independently processed in accordance with any one of the processes of Claims 8 to 11.
-20 -
13.A process according to Claim 12, wherein the at least two streams are directed to the first fractionation.
14.A process according to Claim 12 or 13, wherein reboil in the second fractionation is provided at least in part by heat exchange with at least one of the at least two streams.
15.A process according to Claim 14, wherein the at least one stream used for heat exchange is fed to an intermediate stage of the first fractionation.
16. A process according to Claim 15, wherein at least one of the at least two streams is not used for heat exchange in the second fractionation and is fed to a bottom stage of the first fractionation.
17.A process according to any one of the preceding claims, wherein reboil in the second fractionation is provided at least in part by heat exchange during the partial condensing of the overhead vapour stream.
18.A process according to Claim 17, wherein the heat exchange is between the overhead vapour stream and a liquid product of the second fractionation.
19.A process according to any one of the preceding claims, wherein the first fractionation is at a pressure in the range of 5 to 30 bar (0.5 to 3.0 MPa).
20. A process according to any one of the preceding claims, wherein in step (iv) the first stream is expanded to form a two-phase feed for feeding to the second fractionation.
21. A process according to any one of the preceding claims, wherein in step (iv) the second stream is expanded to form a two-phase feed and reheated via heat exchange for feeding to the second fractionation. -21 -
22.A process according to Claim 21, wherein the second stream is reheated via heat exchange with the condensed product from the first fractionation and/or the overhead vapour stream from the first fractionation.
23.A process according to any one of the preceding claims, wherein the first stream in step (iv) is fed to the second fractionation at a higher stage than the second stream.
24. A process according to any one of the preceding claims, wherein the nitrogen rich stream from the second fractionation is reheated by heat exchange with the overhead vapour stream from step (ii) and/or the separated vapour stream from step (iii).
25. A process according to any one of the preceding claims, wherein the hydrocarbon product stream is removed as an at least partly liquefied product.
26.A process according to any one of the preceding claims, wherein the gaseous feed additionally comprises further inert gases.
27. A process according to Claim 26, wherein the gaseous feed comprises helium.
28.A process according to any one of the preceding claims, wherein the gaseous hydrocarbon feed is pre-treated to remove impurities and/or other unwanted components which solidify in the first and second fractionations.
29.An apparatus for the separation of nitrogen from a gaseous feed comprising a mixture of hydrocarbons and nitrogen gas, the apparatus comprising of: (i) means for cooling and at least partially condensing the gaseous feed; (ii) a first fractionator for producing an overhead vapour stream and a condensed product and a second fractionator operable at a lower pressure than the first fractionator; -22 - (iii) means for conveying the cooled and at least partially condensed feed from step (I) to the first fractionator; (iv) means for conveying the condensed product from the first fractionator to the second fractionator; (v) means for partially condensing the overhead vapour stream, and means for separating the partially condensed vapour stream to provide a liquid stream, and a separated vapour stream; (vi) means for conveying the liquid stream to the first fractionator which is used to provide reflux to the first fractionation, and means for conveying and condensing the separated vapour stream to provide reflux to the second fractionator; and (vii) means for dividing the condensed product of the first fractionator, prior to entry into the second fractionator, into at least two streams; (viii) means for expanding a first stream prior to entry thereof into the second fractionator, and means for expanding and reheating a second stream prior to entry thereof into the second fractionator; (ix) means for conveying a hydrocarbon product low in nitrogen from the second fractionator; and (x) means for conveying a nitrogen rich stream from the second fractionator.
30.An apparatus according to Claim 29, wherein the first and second fractionators are in a stacked configuration.
31.An apparatus according to Claim 29, wherein the first and second fractionators are in a non-stacked configuration, allowing reduction on the overall height of the apparatus.
32.An apparatus according to any one of Claims 29 to 31, wherein the second fractionator comprises a reboil heat exchanger.
33.An apparatus according to any one of Claims 29 to 31, wherein the means for expanding the streams comprises liquid or two-phase expansion turbines.
-23 -
34. An apparatus according to any one of Claims 29 to 33 wherein the second stream in step (viii) is reheated in heat exchange with the separated vapour stream from step (v).
33.An apparatus according to any one of Claims 29 to 31, wherein the means for expanding the streams comprises liquid or two-phase expansion turbines.
-23 - 34. An apparatus according to any one of Claims 29 to 33 wherein the second stream in step (viii) is reheated in heat exchange with the separated vapour stream from step (v).
1. A process for the separation of nitrogen from a gaseous feed comprising a mixture of hydrocarbons and nitrogen gas, the process comprising the steps of: (i) cooling and at least partially condensing the gaseous feed; (ii) feeding the cooled and at least partially condensed feed from step (i) to a first fractionation to produce an overhead vapour stream having an enriched nitrogen content and a condensed product having a reduced nitrogen content which is subjected to a second fractionation, which comprises reboil, at a lower pressure than the first fractionation; (iii) partially condensing the overhead vapour stream, and separating to provide a liquid stream, which is used to provide reflux to the first fractionation, and a separated vapour stream, which is condensed to provide reflux to the second fractionation; and (iv) sub-cooling the condensed product of the first fractionation and dividing the resulting sub-cooled product into at least two streams: a first stream being expanded and fed to the second fractionation, and a second stream being expanded and reheated in heat exchange with the separated vapour stream from step (ii) before being fed to the second fractionation; (v) removing a hydrocarbon product stream low in nitrogen from the second fractionation; and (vi) removing a nitrogen rich stream from the second fractionation.
2. A process according to Claim 1, wherein the hydrocarbons in the gaseous feed comprise or consist of methane.
3. A process according to Claim I of Claim 2, wherein the gaseous feed comprises or consists of natural gas.
4. A process according to any one of the preceding claims, wherein the gaseous feed comprises less than 40 mol% nitrogen.
5. A process according to Claim 4, wherein the gaseous feed comprises less than 35 mol% nitrogen.
6. A process according to Claim 5, wherein the gaseous feed comprises less than mol% nitrogen.
7. A process according to any one of the preceding claims, wherein the gaseous feed comprises at least 20 mol% nitrogen.
8. A process according to any one of the preceding claims, wherein reboil in the second fractionation is provided at least in part by heat exchange during cooling of the gaseous feed.
9. A process according to any one of the preceding claims, wherein the gaseous feed is cooled and at least partially condensed via heat exchange with the hydrocarbon product stream low in nitrogen from the second fractionation and/or the nitrogen rich stream from the second fractionation.
10.A process according to Claim 9, wherein the hydrocarbon product stream low in nitrogen is pumped to elevated pressure and evaporated to provide cooling for the gaseous feed.
11.A process according to any one of the preceding claims, wherein the gaseous feed is expanded prior to the first fractionation.
12.A process according to any one of the preceding claims, wherein the gaseous feed is split into at least two streams, and each stream is independently processed in accordance with any one of the processes of Claims 8 to 11.
-20 - 13.A process according to Claim 12, wherein the at least two streams are directed to the first fractionation.
14.A process according to Claim 12 or 13, wherein reboil in the second fractionation is provided at least in part by heat exchange with at least one of the at least two streams.
15.A process according to Claim 14, wherein the at least one stream used for heat exchange is fed to an intermediate stage of the first fractionation.
16. A process according to Claim 15, wherein at least one of the at least two streams is not used for heat exchange in the second fractionation and is fed to a bottom stage of the first fractionation.
17.A process according to any one of the preceding claims, wherein reboil in the second fractionation is provided at least in part by heat exchange during the partial condensing of the overhead vapour stream.
18.A process according to Claim 17, wherein the heat exchange is between the overhead vapour stream and a liquid product of the second fractionation.
19.A process according to any one of the preceding claims, wherein the first fractionation is at a pressure in the range of 5 to 30 bar (0.5 to 3.0 MPa).
20. A process according to any one of the preceding claims, wherein in step (iv) the first stream is expanded to form a two-phase feed for feeding to the second fractionation.
21. A process according to any one of the preceding claims, wherein in step (iv) the second stream is expanded to form a two-phase feed and reheated via heat exchange for feeding to the second fractionation. -21 -
22.A process according to Claim 21, wherein the second stream is reheated via heat exchange with the condensed product from the first fractionation and/or the overhead vapour stream from the first fractionation.
23.A process according to any one of the preceding claims, wherein the first stream in step (iv) is fed to the second fractionation at a higher stage than the second stream.
24. A process according to any one of the preceding claims, wherein the nitrogen rich stream from the second fractionation is reheated by heat exchange with the overhead vapour stream from step (ii) and/or the separated vapour stream from step (iii).
25. A process according to any one of the preceding claims, wherein the hydrocarbon product stream is removed as an at least partly liquefied product.
26.A process according to any one of the preceding claims, wherein the gaseous feed additionally comprises further inert gases.
27. A process according to Claim 26, wherein the gaseous feed comprises helium.
28.A process according to any one of the preceding claims, wherein the gaseous hydrocarbon feed is pre-treated to remove impurities and/or other unwanted components which solidify in the first and second fractionations.
29.An apparatus for the separation of nitrogen from a gaseous feed comprising a mixture of hydrocarbons and nitrogen gas, the apparatus comprising of: (i) means for cooling and at least partially condensing the gaseous feed; (ii) a first fractionator for producing an overhead vapour stream and a condensed product and a second fractionator operable at a lower pressure than the first fractionator; -22 - (iii) means for conveying the cooled and at least partially condensed feed from step (I) to the first fractionator; (iv) means for conveying the condensed product from the first fractionator to the second fractionator; (v) means for partially condensing the overhead vapour stream, and means for separating the partially condensed vapour stream to provide a liquid stream, and a separated vapour stream; (vi) means for conveying the liquid stream to the first fractionator which is used to provide reflux to the first fractionation, and means for conveying and condensing the separated vapour stream to provide reflux to the second fractionator; and (vii) means for dividing the condensed product of the first fractionator, prior to entry into the second fractionator, into at least two streams; (viii) means for expanding a first stream prior to entry thereof into the second fractionator, and means for expanding and reheating a second stream prior to entry thereof into the second fractionator; (ix) means for conveying a hydrocarbon product low in nitrogen from the second fractionator; and (x) means for conveying a nitrogen rich stream from the second fractionator.
30.An apparatus according to Claim 29, wherein the first and second fractionators are in a stacked configuration.
31.An apparatus according to Claim 29, wherein the first and second fractionators are in a non-stacked configuration, allowing reduction on the overall height of the apparatus.
32.An apparatus according to any one of Claims 29 to 31, wherein the second fractionator comprises a reboil heat exchanger.
GB0905124A 2009-03-25 2009-03-25 Process and apparatus for separation of hydrocarbons and nitrogen Active GB2455462B (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
GB0905124A GB2455462B (en) 2009-03-25 2009-03-25 Process and apparatus for separation of hydrocarbons and nitrogen
EP10755496A EP2433075A2 (en) 2009-03-25 2010-03-23 Process and apparatus for separation of hydrocarbons and nitrogen
US13/259,355 US20120090355A1 (en) 2009-03-25 2010-03-23 Process and apparatus for separation of hydrocarbons and nitrogen
PCT/GB2010/050488 WO2010109228A2 (en) 2009-03-25 2010-03-23 Process and apparatus for separation of hydrocarbons and nitrogen

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB0905124A GB2455462B (en) 2009-03-25 2009-03-25 Process and apparatus for separation of hydrocarbons and nitrogen

Publications (3)

Publication Number Publication Date
GB0905124D0 GB0905124D0 (en) 2009-05-06
GB2455462A true GB2455462A (en) 2009-06-17
GB2455462B GB2455462B (en) 2010-01-06

Family

ID=40640137

Family Applications (1)

Application Number Title Priority Date Filing Date
GB0905124A Active GB2455462B (en) 2009-03-25 2009-03-25 Process and apparatus for separation of hydrocarbons and nitrogen

Country Status (4)

Country Link
US (1) US20120090355A1 (en)
EP (1) EP2433075A2 (en)
GB (1) GB2455462B (en)
WO (1) WO2010109228A2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20110041389A1 (en) * 2009-08-21 2011-02-24 Linde Ag Process for Separating Off Nitrogen from Natural Gas
US20110209499A1 (en) * 2008-11-06 2011-09-01 Linde Aktiengesellschaft Method for removing nitrogen

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9726426B2 (en) 2012-07-11 2017-08-08 Butts Properties, Ltd. System and method for removing excess nitrogen from gas subcooled expander operations
FR3012211B1 (en) * 2013-10-18 2018-11-02 L'air Liquide,Societe Anonyme Pour L'etude Et L'exploitation Des Procedes Georges Claude PROCESS FOR DEAZATING NATURAL GAS WITH OR WITHOUT RECOVERING HELIUM
MX2017001188A (en) * 2014-07-29 2017-05-03 Linde Ag Method and system for recovery of methane from hydrocarbon streams.
DE102015004120A1 (en) * 2015-03-31 2016-10-06 Linde Aktiengesellschaft Process for separating nitrogen from a hydrocarbon-rich fraction
FR3039080B1 (en) * 2015-07-23 2019-05-17 L'air Liquide, Societe Anonyme Pour L'etude Et L'exploitation Des Procedes Georges Claude METHOD OF PURIFYING HYDROCARBON-RICH GAS
US10520250B2 (en) 2017-02-15 2019-12-31 Butts Properties, Ltd. System and method for separating natural gas liquid and nitrogen from natural gas streams
FR3075940B1 (en) * 2017-12-21 2020-05-22 L'air Liquide, Societe Anonyme Pour L'etude Et L'exploitation Des Procedes Georges Claude PROCESS FOR LIQUEFACTION OF A NITROGEN-CONTAINING NATURAL GAS STREAM
FR3075939B1 (en) 2017-12-21 2020-06-19 L'air Liquide, Societe Anonyme Pour L'etude Et L'exploitation Des Procedes Georges Claude PROCESS FOR PRODUCING PURE NITROGEN FROM A NITROGEN-CONTAINING NATURAL GAS STREAM
US11015865B2 (en) 2018-08-27 2021-05-25 Bcck Holding Company System and method for natural gas liquid production with flexible ethane recovery or rejection
CN110131964B (en) * 2019-05-21 2020-09-29 中石化炼化工程(集团)股份有限公司 Chemical-looping air separation method and system
US11674749B2 (en) * 2020-03-13 2023-06-13 Air Products And Chemicals, Inc. LNG production with nitrogen removal
FR3121743B1 (en) 2021-04-09 2023-04-21 Air Liquide Process and apparatus for separating a mixture containing at least nitrogen and methane
US11635255B1 (en) 2022-04-08 2023-04-25 Axip Energy Services, Lp Liquid or supercritical carbon dioxide capture from exhaust gas

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4415345A (en) * 1982-03-26 1983-11-15 Union Carbide Corporation Process to separate nitrogen from natural gas
US4936888A (en) * 1989-12-21 1990-06-26 Phillips Petroleum Company Nitrogen rejection unit
GB2298034A (en) * 1995-02-10 1996-08-21 Air Prod & Chem Dual column process to remove nitrogen from natural gas

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3210951A (en) * 1960-08-25 1965-10-12 Air Prod & Chem Method for low temperature separation of gaseous mixtures
DE1601257B1 (en) * 1968-01-26 1970-10-01 Messer Griesheim Gmbh Process for the low-temperature rectification of a gas mixture
DE2110417A1 (en) * 1971-03-04 1972-09-21 Linde Ag Process for liquefying and subcooling natural gas
US4664686A (en) * 1986-02-07 1987-05-12 Union Carbide Corporation Process to separate nitrogen and methane
US4878932A (en) * 1989-03-21 1989-11-07 Union Carbide Corporation Cryogenic rectification process for separating nitrogen and methane
US5771714A (en) * 1997-08-01 1998-06-30 Praxair Technology, Inc. Cryogenic rectification system for producing higher purity helium
FR2802825B1 (en) * 1999-12-23 2002-05-03 Air Liquide DISTILLATION SEPARATION APPARATUS AND METHOD FOR CLEANING A CONDENSER VAPORIZER OF THE APPARATUS
GB0000327D0 (en) * 2000-01-07 2000-03-01 Costain Oil Gas & Process Limi Hydrocarbon separation process and apparatus
FR2826969B1 (en) * 2001-07-04 2006-12-15 Technip Cie PROCESS FOR THE LIQUEFACTION AND DEAZOTATION OF NATURAL GAS, THE INSTALLATION FOR IMPLEMENTATION, AND GASES OBTAINED BY THIS SEPARATION
GB0220791D0 (en) 2002-09-06 2002-10-16 Boc Group Plc Nitrogen rejection method and apparatus

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4415345A (en) * 1982-03-26 1983-11-15 Union Carbide Corporation Process to separate nitrogen from natural gas
US4936888A (en) * 1989-12-21 1990-06-26 Phillips Petroleum Company Nitrogen rejection unit
GB2298034A (en) * 1995-02-10 1996-08-21 Air Prod & Chem Dual column process to remove nitrogen from natural gas

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20110209499A1 (en) * 2008-11-06 2011-09-01 Linde Aktiengesellschaft Method for removing nitrogen
US20110041389A1 (en) * 2009-08-21 2011-02-24 Linde Ag Process for Separating Off Nitrogen from Natural Gas

Also Published As

Publication number Publication date
WO2010109228A3 (en) 2013-04-04
US20120090355A1 (en) 2012-04-19
WO2010109228A2 (en) 2010-09-30
GB0905124D0 (en) 2009-05-06
GB2455462B (en) 2010-01-06
EP2433075A2 (en) 2012-03-28

Similar Documents

Publication Publication Date Title
GB2455462A (en) Process and Apparatus for Separation of Hydrocarbons and Nitrogen
US9534837B2 (en) Nitrogen removal with ISO-pressure open refrigeration natural gas liquids recovery
US6453698B2 (en) Flexible reflux process for high NGL recovery
KR100939515B1 (en) Dual stage nitrogen rejection from liquefied natural gas
US6755965B2 (en) Ethane extraction process for a hydrocarbon gas stream
US7152430B1 (en) Method of separating CO2 from hydrocarbon gas
KR101657410B1 (en) Integrated nitrogen removal in the production of liquefied natural gas using intermediate feed gas separation
AU2016231621B2 (en) Process and apparatus for separation of hydrocarbons and nitrogen
EP0994318A2 (en) Method and apparatus for enhancing carbon dioxide recovery
US20200088465A1 (en) Helium Extraction from Natural Gas
US20170299261A1 (en) Liquid nitrogen production
US20110048067A1 (en) Natural gas liquefaction method with high-pressure fractionation
US6425266B1 (en) Low temperature hydrocarbon gas separation process
US6467306B2 (en) Process and apparatus for the separation of carbon monoxide and hydrogen from a gaseous mixture thereof
US20160054054A1 (en) Process and apparatus for separation of hydrocarbons and nitrogen
US9851142B2 (en) Method and appliance for separating a mixture containing carbon dioxide by cryogenic distillation
AU2009313087B2 (en) Method for removing nitrogen
JP2001099566A (en) Method for collecting refined flow and production of electronics grade oxygen