EP2997116A1 - Apparatus and process to condition natural gas for transportation - Google Patents
Apparatus and process to condition natural gas for transportationInfo
- Publication number
- EP2997116A1 EP2997116A1 EP14798142.7A EP14798142A EP2997116A1 EP 2997116 A1 EP2997116 A1 EP 2997116A1 EP 14798142 A EP14798142 A EP 14798142A EP 2997116 A1 EP2997116 A1 EP 2997116A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- natural gas
- temperature
- hydrates
- flow
- hydrate formation
- 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.)
- Withdrawn
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L3/00—Gaseous fuels; Natural gas; Synthetic natural gas obtained by processes not covered by subclass C10G, C10K; Liquefied petroleum gas
- C10L3/06—Natural gas; Synthetic natural gas obtained by processes not covered by C10G, C10K3/02 or C10K3/04
- C10L3/10—Working-up natural gas or synthetic natural gas
- C10L3/108—Production of gas hydrates
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L3/00—Gaseous fuels; Natural gas; Synthetic natural gas obtained by processes not covered by subclass C10G, C10K; Liquefied petroleum gas
- C10L3/06—Natural gas; Synthetic natural gas obtained by processes not covered by C10G, C10K3/02 or C10K3/04
- C10L3/10—Working-up natural gas or synthetic natural gas
- C10L3/107—Limiting or prohibiting hydrate formation
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G5/00—Recovery of liquid hydrocarbon mixtures from gases, e.g. natural gas
- C10G5/06—Recovery of liquid hydrocarbon mixtures from gases, e.g. natural gas by cooling or compressing
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J3/00—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification
- F25J3/06—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by partial condensation
- F25J3/0605—Processes 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 feed stream
- F25J3/061—Natural gas or substitute natural gas
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L2290/00—Fuel preparation or upgrading, processes or apparatus therefore, comprising specific process steps or apparatus units
- C10L2290/06—Heat exchange, direct or indirect
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L2290/00—Fuel preparation or upgrading, processes or apparatus therefore, comprising specific process steps or apparatus units
- C10L2290/54—Specific separation steps for separating fractions, components or impurities during preparation or upgrading of a fuel
Definitions
- the present invention relates to a method of conditioning natural gas.
- the present invention relates to a method of conditioning natural gas to reduce the formation of hydrates during the transportation of the gas.
- Raw natural gas as it exists when first extracted from a well, typically undergoes processing before being transported.
- the natural gas primarily consists of methane, but also includes large amounts of water and often heavier hydrocarbons as well. Changes in pressure or temperature during transportation can result in water and/or hydrocarbons condensing. This is undesirable as the hydrocarbons and water may combine to form solid hydrates.
- Hydrates arc stable solids with an appearance and properties similar to ice. They typically form at temperatures between 0°C and 8°C. although depending on the gas composition and pressure they can form at temperatures as high as 15°C. Such hydrates are problematic as they can form blockages in pipes and damage valves and other components, particularly when the natural gas is being transported through a pipe system.
- One current method of conditioning natural gas is to pass the gas through a process known as dewpoint control.
- This process may remove heavier hydrocarbons in addition to water, and involves cooling the gas to a temperature slightly below any temperature expected to be encountered in its subsequent handling. During this cooling process, water and hydrocarbons will condense out and arc removed from the gas. however the temperature is not reduced to where hydrates form. In subsequent transport and handling of the gas, provided it is not cooled below its dewpoint temperature, no further condensation can occur. [00041] This process, however, assumes that the expected transport temperature is above the hydrate formation temperature. Cold climates can therefore cause problems when the required temperature is low enough to allow hydrates to form.
- glycol absorption the most common method of removing water from natural gas. also known as dehydration, is glycol absorption. The process involves bringing natural gas into contact with glycol, which absorbs the water from the natural gas. The glycol is then removed, regenerated and returned to absorb more water. Another method also commonly used involves a similar process with a solid desiccant instead of glycol. Other processes use pressure difference across membranes.
- the current invention aims at providing a cheaper alternative that is practical to operate at a small scale. This will allow economical processing of natural gas at the well head of individual wells or in small fields where building a full scale dehydration plant is not feasible.
- the present invention seeks to provide an improved, or at least an alternative to known, method of conditioning natural gas to reduce hydrate formation during transportation.
- the present invention also seeks to provide a conditioning assembly to condition a flow of natural gas.
- the reference in this specification to any prior publication (or information derived from it), or to any matter which is known, is not, and should not be taken as. an acknowledgement or admission or any form of suggestion that prior publication (or information derived from it) or known matter forms part of the common general knowledge in the field of endeavour to which this specification relates.
- the present invention provides a method of conditioning natural gas to reduce subsequent hydrate formation, the method including the steps of: cooling the natural gas to a temperature at or below the hydrate formation temperature; and
- the subsequent cooling occurs during transportation of the natural gas.
- cooling the natural gas includes introducing a flow of natural gas to a heat exchanger wherein the flow of natural gas is cooled via indirect heat transfer.
- the hydrates form on. and are removed from, the surfaces of the heal exchanger.
- water included in the natural gas condenses during cooling.
- the cooling occurs in at. least two stages:
- the natural gas is cooled to a temperature below hydrate formation temperature such that hydrates form and are collected.
- the natural gas is cooled in the first stage to a temperature about 3 to 5K above the hydrate formation temperature, wherein the hydrate formation temperature is typically between 0°C and 8°C.
- the hydrates are collected by warming the heat exchanger such that hydrates melt and the resulting liquid is collected.
- a constant flow of natural gas is conditioned by alternating the flow of natural gas between at least two heat exchangers configured in a parallel arrangement.
- the present invention provides a conditioning assembly to condition a flow of natural gas to reduce hydrate formation for transportation, the conditioning assembly including:
- a housing including an inlet for introducing a flow of natural gas and an outlet for delivering conditioned gas capable of containing natural gas at or above atmospheric pressure;
- At least one heat exchanger contained within the housing configured to cool the flow of natural gas to a temperature below hydrate formation temperature
- a collection arrangement to remove hydrates from the housing that form during cooling of the natural gas.
- the heat exchanger is a tube and fin style heat exchanger, wherein the hydrates form on the surfaces of the fins and on the outside of the tubes.
- the conditioning assembly includes at least two zones:
- the natural gas is cooled in the first zone to a temperature about 3 to 5K above the hydrate formation temperature, wherein the hydrate formation temperature is typically between 0°C and 8°C.
- hydrates are removed by ceasing the flow of the natural gas, warming the heat exchanger and collecting the resulting liquid.
- Figure 1 is a schematic of a processing plant including two cooling systems operating in parallel.
- the present invention relates to an apparatus and process of cooling natural gas using heat exchangers and allowing liquid waler and solid hydrates to form.
- the water and hydrates arc collected and removed, thereby preventing the formation of hydrates at a later point during transportation.
- This process and or apparatus for conditioning natural gas is well suited to small scale operations where building a traditional, large scale processing plant is not feasible.
- Figure 1 shows a schematic of the conditioning process 1.
- the current embodiment includes a top gas cooler assembly 2 and a bottom gas cooler assembly 3. While the top gas cooler 2 is operating in cooling mode, inlet valve 34 and outlet valve 4 are open, allowing gas to flow from the gas inlet 30, through the gas cooler 2 and out the gas outlet 31.
- Within the gas cooler 2 there are two sections of tubc-and-fin coil type of heat exchanger, high temperature S and low temperature 6, with cooling fluid from a cooling system 33 passing through the tubes 20. cooling the gas which passes outside the tubes and between the fins 21.
- Cooling from the cooling system 33 to the high temperature heat exchanger 5 is controlled so that the gas outlet temperature 7 is approximately 3-5 above the hydrate formation temperature. Cooling from the cooling system 33 to the low temperature heat exchanger 6 is controlled so that the gas outlet temperature S is below the hydrate formation temperature.
- a preferred embodiment may include fins spaced between 3mm and 50mm from one another, a more preferred embodiment with fins spaced between 10mm and 25mm from one another and a yet more preferred embodiment with fins spaced between 1 mm and 20mm from one another.
- the spacing of lubes 20 and fins 21 may be varied through the low temperature heal exchanger 6, according to the predicted gas cooling profile through the heat exchanger
- fin 21 spacing is wider at the gas inlet end 7 of the low temperature heal exchanger 6, as hydrate formation is usually greater at the inlet end 7.
- the fins may be spaced by about 20-30mm from one another at the inlet end 7 of the low temperature heat exchanger, narrowing to about 4- 10mm at the outlet end 8. In another embodiment, the fins may be spaced by about 25-40mm at the inlet end
- the exact fin 21 and tube 20 spacing, and its variation through the low temperature heal exchanger 6, may be different for each particular application due to different gas compositions and different required dewpoinls.
- the tube 20 and fin 21 spacing are also varied depending on the required time for the heat exchanger 6 lo remain in service before defrost, and therefore on the amount of accumulated hydrate required to be held without blockage of gas passages.
- the high temperature heat exchanger 5 may have tubes 20 and fins 21 spaced much closer together than in the low temperature heat exchanger 6. as there is no need to allow for the build up of hydrates on the surfaces.
- a preferred embodiment may include fins spaced between 5mm and 25mm from one another, a more preferred embodimcn with fins spaced between 2mm and 12.5mm from one another and a ycl more preferred embodiment with fins spaced between 7.5mm and 10mm from one another.
- the cooling fluid used within the tubes 20 may be a primary refrigerant which boils within the tubes 20, such as propane, ammonia or one of the many synthetic refrigerants. Alternatively, it may be a secondary single-phase heat transfer fluid such as water, or a fluid with a lower freezing point such as a mixture of water with glycol or an inorganic salt, or a hydrocarbon. Any other suitable cooling fluid suitable for the purpose may also be used, depending on particular requirements for individual installations.
- the design of the current system may allow (depending on the particular local conditions and resulting system design) for the cooling to take place using heat exchangers only, not requiring the use of any valves, throttles, pumps or compressors to significantly alter the working pressure or to alter the temperature using pressure changes.
- top gas cooler 2 While the top gas cooler 2 is in service, gas flow to the bottom gas cooler 3 is stopped, and the bottom gas cooler 3 is warmed to a temperature which is sufficient to melt off accumulated hydrate.
- the hydrate melting temperature is not necessarily the same as the hydrate formation temperature.
- Heat is provided from an available heat source 32. which may include (but is not limited to) waste heat from the cooling system 33.
- the warming may be achieved by any of several methods, depending on the application, including (bu not limited to):
- the hydrates in contact with the heat exchanger will melt first, resulting in hydrates being released from the heal exchanger and collected while still in solid form.
- the hydrates may be completely melted and collected in liquid form only.
- the tubes and fins will preferably be arranged to facilitate the flow of hydrates from the heat exchanger surfaces to the second drain pan. such as by angling the (ins so that fully or partially melted hydrates flow off due to gravity.
- an automatic system to aid in the removal of hydrates may be used, such as a vibration or scraping mechanism, thereby allowing the hydrates to be collected more quickly and reduce the time required for the defrosting mode.
- the bottom gas cooler 3 While the top gas cooler 2 is operating in cooling mode, the bottom gas cooler 3 is in defrosting mode. This takes place by closing outlet valve 42 to stop gas flow through the bottom gas cooler 3. Cooling to both the high temperature 43 and low temperature 44 heat exchangers is stopped by closing valves 49, 50 and the low temperature heat exchanger 44 is heated by opening valves 45 to permit warm fluid to flow from the defrost heat source 32 through heating tubes 22. As the low temperature heat exchanger 44 is warmed by the heating tubes 22, the accumulated hydrate melts, and drains off via the second drain pan 46 for further processing 48 outside the gas cooler 1.
- the time required to fully melt off all hydrate will vary, depending on the amount of hydrate that has accumulated and the temperature of the heat source, but may be typically 30 minutes to 4 hours.
- the valves 45 are closed to slop heating of the low temperature heal exchanger 44, and cooling is re-started by opening valves 49, 50 connected to the cooling system 33.
- the low 44 and high 43 temperature heat exchangers have been cooled again to normal operating temperature for hydrate accumulation, the system is ready for the bottom cooler 3 to be put into gas cooling mode and the top cooler 2 to be taken out of gas cooling mode and the accumulated hydrate melted off.
- the heat exchangers arc contained within a casing 47. which has a design pressure appropriate to the required operating pressure of the gas cooling process. This may be typically in the range 100 kPa g to 10 MPa g , but pressures above or below this range may be used to suit the specific application.
- the process for conditioning natural gas may further include a heat recovery step which provides a means to reduce the overall cooling duty of the process as herein described.
- a heat recovery step which provides the cool outgoing gas from the process may be used to cool a separate working fluid via indirect heal transfer. Once the separate working fluid is cooled, it may then be used to precool the natural gas introduced to the process as herein described again via indirect heat exchange with the separate working fluid. Accordingly, the energy used to cool the natural gas in the process may be recovered to a degree from the gas leaving the process.
- the separate working fluid may be included in a separate working fluid heat recovery circuit where the working fluid is cycled between (wo heal exchangers by means of a pump.
- the first heal exchanger is arranged as a precooling step wherein the working fluid precools the natural gas by indirect heat exchange before being introduced to the process as herein described.
- the working fluid having been heated by the incoming natural gas in the first heat exchanger is then sent to the second of the two heat exchangers in the working fluid heat recovery circuit.
- the working fluid is then cooled by the outgoing gas again by indirect heat exchange in the second heat exchanger after which the working fluid is cycled back to the first heat exchanger.
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Mechanical Engineering (AREA)
- Thermal Sciences (AREA)
- General Engineering & Computer Science (AREA)
- Filling Or Discharging Of Gas Storage Vessels (AREA)
- Heat-Exchange Devices With Radiators And Conduit Assemblies (AREA)
Abstract
Description
Claims
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU2013901680A AU2013901680A0 (en) | 2013-05-13 | Apparatus and process to condition natural gas for transportation | |
| PCT/AU2014/050034 WO2014183165A1 (en) | 2013-05-13 | 2014-05-13 | Apparatus and process to condition natural gas for transportation |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP2997116A1 true EP2997116A1 (en) | 2016-03-23 |
| EP2997116A4 EP2997116A4 (en) | 2016-11-16 |
Family
ID=51897517
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP14798142.7A Withdrawn EP2997116A4 (en) | 2013-05-13 | 2014-05-13 | Apparatus and process to condition natural gas for transportation |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US20160090542A1 (en) |
| EP (1) | EP2997116A4 (en) |
| CA (1) | CA2912435A1 (en) |
| EA (1) | EA201592161A1 (en) |
| WO (1) | WO2014183165A1 (en) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9662609B2 (en) * | 2015-04-14 | 2017-05-30 | Uop Llc | Processes for cooling a wet natural gas stream |
| US9868910B2 (en) * | 2015-06-04 | 2018-01-16 | Exxonmobil Upstream Research Company | Process for managing hydrate and wax deposition in hydrocarbon pipelines |
| US20180266761A1 (en) * | 2017-03-20 | 2018-09-20 | Larry Baxter | Self-Cleaning Desublimating Heat Exchanger for Gas/Vapor Separation |
| US20180328657A1 (en) * | 2017-05-10 | 2018-11-15 | Linde Aktiengesellschaft | Methods for producing pressurized alkene gas |
| US20180328658A1 (en) * | 2017-05-10 | 2018-11-15 | Linde Aktiengesellschaft | Methods for producing pressurized alkene gas |
| US20180328660A1 (en) * | 2017-05-10 | 2018-11-15 | Linde Aktiengesellschaft | Methods for removing impurities from process gas streams |
| US20180328661A1 (en) * | 2017-05-11 | 2018-11-15 | Larry Baxter | Method for Removing Foulants from a Heat Exchanger through Coolant Flow Control |
| KR102272114B1 (en) * | 2019-11-13 | 2021-07-02 | 서울대학교산학협력단 | Method to remove condensed water in gas export pipeline using hydrogel particles |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3354663A (en) * | 1961-06-13 | 1967-11-28 | Atlantic Richfield Co | Hydrate removal from wet natural gas |
| US3282059A (en) * | 1964-01-21 | 1966-11-01 | Chicago Bridge & Iron Co | Method of purging heat exchangers of solidified impurities in the liquefaction of natural gas |
| US3488677A (en) * | 1967-01-17 | 1970-01-06 | Tioga Wells Corp | Process for purification of natural gas |
| US3537270A (en) * | 1967-09-07 | 1970-11-03 | Chevron Res | Natural gas dehydration |
| US3791157A (en) * | 1970-11-09 | 1974-02-12 | Tioga Wells Corp | Process for purification of natural gas |
| CA1252272A (en) * | 1983-05-09 | 1989-04-11 | Satoshi Tanno | Method of manufacturing fin-tube heat exchangers |
| US5664426A (en) * | 1996-02-09 | 1997-09-09 | Pai | Regenerative gas dehydrator |
| US6082133A (en) * | 1999-02-05 | 2000-07-04 | Cryo Fuel Systems, Inc | Apparatus and method for purifying natural gas via cryogenic separation |
| US6350928B1 (en) * | 1999-12-30 | 2002-02-26 | Marathon Oil Company | Production of a gas hydrate slurry using a fluidized bed heat exchanger |
| CN2497857Y (en) * | 2001-09-03 | 2002-07-03 | 吕应中 | Unitary gas dewaterer |
| AU2003900534A0 (en) * | 2003-02-07 | 2003-02-20 | Shell Internationale Research Maatschappij B.V. | Process and apparatus for removal of a contaminant from a natural gas feed stream |
| JP2004244495A (en) * | 2003-02-13 | 2004-09-02 | Mitsubishi Heavy Ind Ltd | Method and system for forming natural gas hydrate |
| US7976613B2 (en) * | 2005-08-16 | 2011-07-12 | Woodside Energy Limited | Dehydration of natural gas in an underwater environment |
| FR2894838B1 (en) * | 2005-12-21 | 2008-03-14 | Gaz De France Sa | METHOD AND SYSTEM FOR CAPTURING CARBON DIOXIDE IN FUMEES |
| DE102008064116A1 (en) * | 2008-12-19 | 2010-07-01 | Linde Aktiengesellschaft | Process and apparatus for producing clathrate hydrate |
| GB201000097D0 (en) * | 2010-01-05 | 2010-12-29 | Johnson Matthey Plc | Apparatus and process for treating natural gas |
-
2014
- 2014-05-13 EA EA201592161A patent/EA201592161A1/en unknown
- 2014-05-13 CA CA2912435A patent/CA2912435A1/en not_active Abandoned
- 2014-05-13 US US14/891,126 patent/US20160090542A1/en not_active Abandoned
- 2014-05-13 EP EP14798142.7A patent/EP2997116A4/en not_active Withdrawn
- 2014-05-13 WO PCT/AU2014/050034 patent/WO2014183165A1/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| CA2912435A1 (en) | 2014-11-20 |
| EP2997116A4 (en) | 2016-11-16 |
| EA201592161A1 (en) | 2016-06-30 |
| WO2014183165A1 (en) | 2014-11-20 |
| US20160090542A1 (en) | 2016-03-31 |
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