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Natural-gas processing

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Industrial processes designed to purify raw natural gas
A natural-gas processing plant in Aderklaa, Austria

Natural-gas processing is a range of industrial processes designed to purify rawnatural gas by removing contaminants such as solids,water,carbon dioxide (CO2),hydrogen sulfide (H2S), mercury and highermolecular mass hydrocarbons (condensate) to producepipeline quality dry natural gas[1] for pipeline distribution and final use.[2] Some of the substances which contaminate natural gas have economic value and are further processed or sold. Hydrocarbons that are liquid at ambient conditions: temperature and pressure (i.e.,pentane and heavier) are callednatural-gas condensate (sometimes also callednatural gasoline or simplycondensate).

Raw natural gas comes primarily from three types of wells: crudeoil wells, gas wells, andcondensate wells.Crude oil and natural gas are often found together in the same reservoir. Natural gas produced in wells with crude oil is generally classified asassociated-dissolved gas as the gas had been associated with or dissolved incrude oil. Natural gas production not associated with crude oil is classified as “non-associated.” In 2009, 89 percent of U.S.wellhead production of natural gas was non-associated.[3] Non-associated gas wells producing a dry gas in terms ofcondensate and water can send the dry gas directly to a pipeline or gas plant without undergoing any separation processIng allowing immediateuse.[4]

Natural-gas processing begins underground or at the well-head. In a crude oil well, natural gas processing begins as the fluid loses pressure and flows through the reservoir rocks until it reaches the well tubing.[5] In other wells, processing begins at the wellhead which extracts the composition of natural gas according to the type, depth, and location of the underground deposit and the geology of the area.[2]

Natural gas when relatively free ofhydrogen sulfide is calledsweet gas; natural gas that contains elevated hydrogen sulfide levels is calledsour gas; natural gas, or any other gas mixture, containing significant quantities of hydrogen sulfide or carbon dioxide or similar acidic gases, is calledacid gas.

Types of raw-natural-gas wells

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  • Crudeoil wells: Natural gas that comes from crude oil wells is typically calledassociated gas. This gas could exist as a separate gas cap above the crude oil in the underground reservoir or could be dissolved in the crude oil, ultimately coming out of solution as the pressure is reduced during production. Condensate produced from oil wells is often referred to aslease condensate.[6]
  • Dry gas wells: These wells typically produce only raw natural gas that contains no condensate with little to no crude oil and are callednon-associated gas. Condensate from dry gas is extracted at gas processing plants and is often calledplant condensate.[6]
  • Condensate wells: These wells typically produce raw natural gas along withnatural gas liquid with little to no crude oil and are callednon-associated gas. Such raw natural gas is often referred to aswet gas.
  • Coal seam wells: These wells typically produce raw natural gas from methane deposits in the pores of coal seams, often existing underground in a more concentrated state ofadsorption onto the surface of the coal itself. Such gas is referred to ascoalbed gas orcoalbed methane (coal seam gas in Australia). Coalbed gas has become an important source of energy in recent decades.

Contaminants in raw natural gas

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See also:Natural-gas condensate

Raw natural gas typically consists primarily ofmethane (CH4) andethane (C2H6), the shortest and lightesthydrocarbon molecules. It often also contains varying amounts of:

Natural gas quality standards

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Raw natural gas must be purified to meet the quality standards specified by the majorpipeline transmission and distribution companies. Those quality standards vary from pipeline to pipeline and are usually a function of a pipeline system's design and the markets that it serves. In general, the standards specify that the natural gas:

  • Be within a specific range of heating value (caloric value). For example, in the United States, it should be about 1035 ± 5%BTU per cubic foot of gas at 1 atmosphere and 60 °F (41MJ ± 5% per cubic metre of gas at 1 atmosphere and 15.6 °C). In the United Kingdom the grosscalorific value must be in the range 37.0 – 44.5 MJ/m3 for entry into theNational Transmission System (NTS).[9]
  • Be delivered at or above a specifiedhydrocarbon dew point temperature (below which some of the hydrocarbons in the gas might condense at pipeline pressure forming liquid slugs that could damage the pipeline.) Hydrocarbon dew-point adjustment reduces the concentration of heavy hydrocarbons so no condensation occurs during the ensuing transport in the pipelines. In the UK the hydrocarbon dew point is defined as <-2 °C for entry into the NTS.[9] The hydrocarbon dewpoint changes with the prevailing ambient temperature, the seasonal variation is:[10]
Seasonal variation of hydrocarbon dewpoint
Hydrocarbon dewpoint30 °F (–1.1 °C)35 °F (1.7 °C)40 °F (4.4 °C)45 °F (7.2 °C)50 °F (10 °C)
MonthsDecember

January

February

March

April

November

May

October

June

September

July

August

The natural gas should:

  • Be free of particulate solids and liquid water to prevent erosion, corrosion or other damage to the pipeline.
  • Be dehydrated of water vapor sufficiently to prevent the formation of methane hydrates within the gas processing plant or subsequently within the sales gas transmission pipeline. A typical water content specification in the U.S. is that gas must contain no more than seven pounds of water per millionstandard cubic feet of gas.[11][12] In the UK this is defined as <-10 °C @ 85barg for entry into the NTS.[9]
  • Contain no more than trace amounts of components such as hydrogen sulfide, carbon dioxide, mercaptans, and nitrogen. The most common specification for hydrogen sulfide content is 0.25grain H2S per 100 cubic feet of gas, or approximately 4 ppm. Specifications for CO2 typically limit the content to no more than two or three percent. In the UK hydrogen sulfide is specified ≤5 mg/m3 and total sulfur as ≤50 mg/m3, carbon dioxide as ≤2.0% (molar), and nitrogen as ≤5.0% (molar) for entry into the NTS.[9]
  • Maintain mercury at less than detectable limits (approximately 0.001ppb by volume) primarily to avoid damaging equipment in the gas processing plant or the pipeline transmission system from mercury amalgamation and embrittlement of aluminum and other metals.[7][13][14]

Description of a natural-gas processing plant

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There are a variety of ways in which to configure the variousunit processes used in the treatment of raw natural gas. Theblock flow diagram below is a generalized, typical configuration for the processing of raw natural gas from non-associated gas wells showing how raw natural gas is processed into sales gas piped to the end user markets.[15][16][17][18][19] and various byproducts:

Raw natural gas is commonly collected from a group of adjacent wells and is first processed in a separator vessels at that collection point for removal of free liquid water andnatural gas condensate.[23] The condensate is usually then transported to an oil refinery and the water is treated and disposed of as wastewater.

The raw gas is then piped to a gas processing plant where the initial purification is usually the removal of acid gases (hydrogen sulfide and carbon dioxide). There are several processes available for that purpose as shown in the flow diagram, butamine treating is the process that was historically used. However, due to a range of performance and environmental constraints of the amine process, a newer technology based on the use ofpolymeric membranes to separate the carbon dioxide and hydrogen sulfide from the natural gas stream has gained increasing acceptance. Membranes are attractive since no reagents are consumed.[24]

The acid gases, if present, are removed by membrane or amine treating and can then be routed into a sulfur recovery unit which converts the hydrogen sulfide in the acid gas into either elemental sulfur or sulfuric acid. Of the processes available for these conversions, theClaus process is by far the most well known for recovering elemental sulfur, whereas the conventionalContact process and the WSA (Wet sulfuric acid process) are the most used technologies for recoveringsulfuric acid. Smaller quantities of acid gas may be disposed of by flaring.

The residual gas from the Claus process is commonly calledtail gas and that gas is then processed in a tail gas treating unit (TGTU) to recover and recycle residual sulfur-containing compounds back into the Claus unit. Again, as shown in the flow diagram, there are a number of processes available for treating the Claus unit tail gas and for that purpose a WSA process is also very suitable since it can work autothermally on tail gases.

The next step in the gas processing plant is to remove water vapor from the gas using either the regenerableabsorption in liquidtriethylene glycol (TEG),[12] commonly referred to asglycol dehydration, deliquescent chloride desiccants, and or aPressure Swing Adsorption (PSA) unit which is regenerableadsorption using a solid adsorbent.[25] Other newer processes likemembranes may also be considered.

Mercury is then removed by using adsorption processes (as shown in the flow diagram) such asactivated carbon or regenerablemolecular sieves.[7]

Although not common, nitrogen is sometimes removed and rejected using one of the three processes indicated on the flow diagram:

  • Cryogenic process (Nitrogen Rejection Unit),[26] using low temperaturedistillation. This process can be modified to also recover helium, if desired (see alsoindustrial gas).
  • Absorption process,[27] using lean oil or a special solvent[28] as the absorbent.
  • Adsorption process, using activated carbon or molecular sieves as the adsorbent. This process may have limited applicability because it is said to incur the loss of butanes and heavier hydrocarbons.

NGL fractionation train

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The NGL fractionation process treats offgas from the separators at anoil terminal or the overhead fraction from a crude distillation column in arefinery. Fractionation aims to produce useful products including natural gas suitable for piping to industrial and domestic consumers;liquefied petroleum gases (Propane and Butane) for sale; andgasoline feedstock for liquid fuel blending.[29] The recovered NGL stream is processed through a fractionation train consisting of up to five distillation towers in series: ademethanizer, adeethanizer, adepropanizer, adebutanizer and abutane splitter. The fractionation train typically uses a cryogenic low temperature distillation process involving expansion of the recovered NGL through aturbo-expander followed by distillation in a demethanizingfractionating column.[30][31] Some gas processing plants use lean oil absorption process[27] rather than the cryogenic turbo-expander process.

The gaseous feed to the NGL fractionation plant is typically compressed to about 60bar and 37 °C.[32] The feed is cooled to -22 °C, by exchange with the demethanizer overhead product and by a refrigeration system and is split into three streams:

  • Condensed liquid passes through aJoule-Thomson valve reducing the pressure to 20 bar and enters the demethanizer as the lower feed at -44.7 °C.
  • Some of the vapour is routed through a turbo-expander and enters the demethanizer as the upper feed at -64 °C.
  • The remaining vapor is chilled by the demethanizer overhead product and Joule-Thomson cooling (through a valve) and enters the column asreflux at -96 °C.[32]

The overhead product is mainly methane at 20 bar and -98 °C. This is heated and compressed to yield a sales gas at 20 bar and 40 °C. The bottom product is NGL at 20 barg which is fed to the deethanizer.  

The overhead product from the deethanizer is ethane and the bottoms are fed to the depropanizer. The overhead product from the depropanizer is propane and the bottoms are fed to the debutanizer. The overhead product from the debutanizer is a mixture of normal and iso-butane, and the bottoms product is a C5+ gasoline mixture.

The operating conditions of the vessels in the NGL fractionation train are typically as follows.[29][33][34]

NGL column operating conditions
DemethanizerDeethanizerDepropanizerDebutanizerButane Splitter
Feed pressure60 barg30 barg
Feed temperature37 °C25 °C37 °C125 °C59 °C
Column operating pressure20 barg26-30 barg10-16.2 barg3.8-17 barg4.9-7 barg
Overhead product temperature-98°C50 °C59 °C49 °C
Bottom product temperature12 °C37 °C125 °C118 °C67 °C
Overhead productMethane (natural gas)EthanePropaneButaneIsobutane
Bottom productNatural gas liquids(Depropanizer feed)(Debutanizer feed)GasolineNormal Butane

A typical composition of the feed and product is as follows.[32]

Stream composition, % volume
ComponentFeedNGLEthanePropaneIsobutanen-ButaneGasoline
Methane89.40.51.36
Ethane4.937.095.147.32
Propane2.226.03.590.182.0
Isobutane1.37.22.596.04.5
n-Butane2.214.82.095.03.0
Isopentane5.033.13
n-Pentane3.50.523.52
n-Hexane4.026.9
n-Heptane2.013.45
Total100100100100100100100

Sweetening Units

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The recovered streams of propane, butanes and C5+ may be "sweetened" in aMerox process unit to convert undesirable mercaptans intodisulfides and, along with the recovered ethane, are the final NGL by-products from the gas processing plant. Currently, most cryogenic plants do not include fractionation for economic reasons, and the NGL stream is instead transported as a mixed product to standalone fractionation complexes located near refineries or chemical plants that use the components forfeedstock. In case laying pipeline is not possible for geographical reason, or the distance between source and consumer exceed 3000 km, natural gas is then transported by ship asLNG (liquefied natural gas) and again converted into its gaseous state in the vicinity of the consumer.

Products

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The residue gas from the NGL recovery section is the final, purified sales gas which is pipelined to the end-user markets. Rules and agreements are made between buyer and seller regarding the quality of the gas. These usually specify the maximum allowable concentration of CO2, H2S and H2O as well as requiring the gas to be commercially free from objectionable odours and materials, and dust or other solid or liquid matter, waxes, gums and gum forming constituents, which might damage or adversely affect operation of the buyers equipment. When an upset occurs on the treatment plant buyers can usually refuse to accept the gas, lower the flow rate or re-negotiate the price.

Helium recovery

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If the gas has significanthelium content, the helium may be recovered byfractional distillation. Natural gas may contain as much as 7% helium, and is the commercial source of thenoble gas.[35] For instance, theHugoton Gas Field in Kansas and Oklahoma in the United States contains concentrations of helium from 0.3% to 1.9%, which is separated out as a valuable byproduct.[36]

See also

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References

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  1. ^"PHMSA: Stakeholder Communications - NG Processing Plants".primis.phmsa.dot.gov. Retrieved9 April 2018.
  2. ^abSpeight, James G. (2015).Handbook of Petroleum Product Analysis, Second Edition. Hoboken, NJ: John Wiley & Sons. p. 71.ISBN 978-1-118-36926-5.
  3. ^"Archived copy"(PDF). Archived fromthe original(PDF) on 2016-03-05. Retrieved2014-09-21.{{cite web}}: CS1 maint: archived copy as title (link)
  4. ^Kidnay, Arthur J.; Parrish, William R.; McCartney, Daniel G. (2019).Fundamentals of Natural Gas Processing, Third Edition. Boca Raton, FL: CRC Press. p. 165.ISBN 978-0-429-87715-5.
  5. ^Agency, United States Central Intelligence (1977).Natural Gas. Washington, D.C.: U.S. Central Intelligence Agency. p. 25.
  6. ^abU.S. Crude Oil Production Forecast- Analysis of Crude Types(PDF), Washington, DC: U.S. Energy Information Administration, 29 May 2014, p. 7,A final point to consider involves the distinction between the very light grades of lease condensate (which are included in EIA's oil production data) and hydrocarbon gas liquids (HGL) that are produced from the wellhead as gas but are converted to liquids when separated from methane at a natural gas processing plant. These hydrocarbons include ethane, propane, butanes, and hydrocarbons with five or more carbon atoms – referred to as pentanes plus, naptha, or plant condensate. Plant condensate can also be blended with crude oil, which would change both the distribution and total volume of oil received by refineries.
  7. ^abc"Mercury Removal from Natural Gas and Liquids"(PDF). UOP LLC. Archived fromthe original(PDF) on 2011-01-01.
  8. ^"Radium in Piping".
  9. ^abcd"Gas Safety (Management) Regulations 1996".legislation.co.uk. 1996. Retrieved13 June 2020.
  10. ^Institute of Petroleum (1978).A guide to North Sea oil and gas technology. London: Heyden & Son. p. 133.ISBN 0855013168.
  11. ^Dehydration of Natural GasArchived 2007-02-24 at theWayback Machine by Prof. Jon Steiner Gudmundsson, Norwegian University of Science and Technology
  12. ^abGlycol DehydrationArchived 2009-09-12 at theWayback Machine (includes a flow diagram)
  13. ^Desulfurization of and Mercury Removal From Natural GasArchived 2008-03-03 at theWayback Machine by Bourke, M.J. and Mazzoni, A.F., Laurance Reid Gas Conditioning Conference, Norman, Oklahoma, March 1989.
  14. ^Using Gas Geochemistry to Assess Mercury RiskArchived 2015-08-28 at theWayback Machine, OilTracers, 2006
  15. ^Natural Gas Processing: The Crucial Link Between Natural Gas Production and Its Transportation to MarketArchived 2011-03-04 at theWayback Machine
  16. ^Example Gas PlantArchived 2010-12-01 at theWayback Machine
  17. ^From Purification to Liquefaction Gas ProcessingArchived 2010-01-15 at theWayback Machine
  18. ^"Feed-Gas Treatment Design for the Pearl GTL Project"(PDF).spe.org. Retrieved9 April 2018.
  19. ^Benefits of integrating NGL extraction and LNG liquefactionArchived 2013-06-26 at theWayback Machine
  20. ^"MSDS: Natural gas liquids"(PDF). ConocoPhillips.
  21. ^"What are natural gas liquids and how are they used?". United States Energy Information Administration. April 20, 2012.
  22. ^"Guide to Understanding Natural Gas and Natural Gas Liquids". STI Group. 2014-02-19.
  23. ^"Liquid / Gas Separation Technology - Oil & Gas | Pall Corporation".www.pall.com. Retrieved2023-04-22.
  24. ^Baker, R. W. "Future Directions of Membrane Gas Separation Technology" Ind. Eng. Chem. Res. 2002, volume 41, pages 1393-1411.doi:10.1021/ie0108088
  25. ^Molecular SievesArchived 2011-01-01 at theWayback Machine (includes a flow diagram of a PSA unit)
  26. ^Gas Processes 2002, Hydrocarbon Processing, pages 84–86, May 2002 (schematic flow diagrams and descriptions of the Nitrogen Rejection and Nitrogen Removal processes)
  27. ^abMarket-Driven Evolution of Gas Processing Technologies for NGLs Advanced Extraction Technology Inc. website page
  28. ^AET Process Nitrogen Rejection Unit Advanced Extraction Technology Inc. website page
  29. ^abManley, D. B. (1998). "Thermodynamically efficient distillation: NGL Fractionation".Latin American Applied Research.
  30. ^Cryogenic Turbo-Expander Process Advanced Extraction Technology Inc. website page
  31. ^Gas Processes 2002, Hydrocarbon Processing, pages 83–84, May 2002 (schematic flow diagrams and descriptions of the NGL-Pro and NGL Recovery processes)
  32. ^abcMuneeb Nawaz ‘Synthesis and Design of Demethaniser Flowsheets for Low Temperature Separation Processes,' University of Manchester, unpublished PhD thesis, 2011, pp. 137, 138, 154
  33. ^Luyben, W. L. (2013). "Control of a Train of Distillation Columns for the Separation of natural gas".Industrial and Engineering Chemistry Research.52:5710741–10753.doi:10.1021/ie400869v.
  34. ^ElBadawy, K. M.; Teamah, M. A.; Shehata, A. I.; Hanfy, A. A. (2017). "Simulation of LPG Production from Natural Gas using Fractionation Towers".International Journal of Advanced Scientific and Technical Research.6 (7).
  35. ^Winter, Mark (2008)."Helium: the essentials". University of Sheffield. Retrieved2008-07-14.
  36. ^Dwight E. Ward and Arthur P. Pierce (1973) "Helium" inUnited States Mineral Resources, US Geological Survey, Professional Paper 820, p.285-290.

External links

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Further reading

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  • Haring, H.W. (2008). Industrial Gases Processing. Weinheim, Germany: WILEY-VCH Verlag Gmbh & CO. KGaA
  • Kohl, A., & Nielsen, R. (1997). Gas Purification. 5TH Edition. Houston, Texas: Gulf Publishing Company
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