EP2258814A1 - Procédé de traitement d'un dégagement gazeux Fischer-Tropsch - Google Patents

Procédé de traitement d'un dégagement gazeux Fischer-Tropsch Download PDF

Info

Publication number
EP2258814A1
EP2258814A1 EP09161901A EP09161901A EP2258814A1 EP 2258814 A1 EP2258814 A1 EP 2258814A1 EP 09161901 A EP09161901 A EP 09161901A EP 09161901 A EP09161901 A EP 09161901A EP 2258814 A1 EP2258814 A1 EP 2258814A1
Authority
EP
European Patent Office
Prior art keywords
gas
expander
providing
temperature
effluent
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Withdrawn
Application number
EP09161901A
Other languages
German (de)
English (en)
Inventor
designation of the inventor has not yet been filed The
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.)
Shell Internationale Research Maatschappij BV
Original Assignee
Shell Internationale Research Maatschappij BV
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 Shell Internationale Research Maatschappij BV filed Critical Shell Internationale Research Maatschappij BV
Priority to EP09161901A priority Critical patent/EP2258814A1/fr
Publication of EP2258814A1 publication Critical patent/EP2258814A1/fr
Withdrawn legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G2/00Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon
    • C10G2/30Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon from carbon monoxide with hydrogen

Definitions

  • the present invention pertains to a process for processing Fischer-Tropsch off-gas.
  • the Fischer-Tropsch process can be used for the conversion of hydrocarbonaceous feed stocks into normally liquid and/or solid hydrocarbons (0 °C, 1 bar).
  • the feed stock e.g. natural gas, associated gas, coal-bed methane, residual oil fractions, biomass and/or coal
  • the feed stock is converted in a first step into a mixture of hydrogen and carbon monoxide. This mixture is often referred to as synthesis gas or syngas.
  • the synthesis gas is fed into a reactor where it is converted over a suitable catalyst at elevated temperature and pressure into paraffinic compounds ranging from methane to high molecular weight modules comprising up to 200 carbon atoms, or, under particular circumstances, even more.
  • hydrocarbon products manufactured in the Fischer-Tropsch process are processed into different fractions, for example, a liquid hydrocarbon stream comprising mainly C 3 + hydrocarbons, and a gaseous hydrocarbon stream which comprises carbon monoxide, unconverted methane, and lower hydrocarbons.
  • the gaseous hydrocarbon stream is generally at high temperature and pressure and contains combustible components. It can thus serve as a source for generating energy.
  • EP1004561 describes a process for producing normally liquid hydrocarbons comprising the steps of manufacturing syngas by partial oxidation of hydrocarbonaceous feeds at elevated temperature and pressure, catalytically converting the syngas into, int. al., normally liquid hydrocarbons and normally gaseous hydrocarbons, and expanding and/or combusting at least part of the normally gaseous hydrocarbons, and any unconverted syngas and/or hydrocarbonaceous feeds, to provide power for compersing the hydrocarbonaceous feed used in the syngas manufacture.
  • WO99/15483 describes a process for producing normally liquid hydrocarbons comprising the steps of manufacturing syngas by partial oxidation of hydrocarbonaceous feeds using pressurised oxygen, quenching and/or cooling the syngas with water recycled from further on in the process, catalytically converting the syngas into normally liquid hydrocarbons, normally gaseous hydrocarbons and water, recycling the water to the syngas manufacturing step, and expanding and/or combusting at least part of the normally gaseous hydrocarbons, and any unconverted syngas and/or hydrocarbonaceous feeds, to provide power for compressing oxygen used in the syngas manufacture.
  • NL7413678 describes a process for producing normally liquid hydrocarbons comprising the steps of manufacturing syngas by partial oxidation of hydrocarbonaceous feeds cooling the syngas, removing solid particles and sulphur compounds from the gas, and catalytically converting the syngas into normally liquid hydrocarbons, normally gaseous hydrocarbons and water.
  • the product from the synthesis is cooled down at a pressure in the range of 20-40 ata to a temperature of -30 to -70 °C, and may then be separated into a liquid containing C 3 + hydrocarbons and a gas containing unconverted hydrogen, carbon monoxide, nitrogen and C 1 -C 2 hydrocarbons.
  • the gas is expanded in a back-pressure turbine, preferably after heating to a temperature ranging from -20 to -10 °C whereupon it cools to a temperature ranging from -50 to - 70 °C. It is indicated that the back pressure turbine may be used to generate energy that can be used in the system.
  • the present invention provides such a process.
  • the present invention pertains to a process for processing Fischer-Tropsch off-gas which comprises the steps of
  • Fischer-Tropsch off-gas as it originates from the Fischer-Tropsh process comprises hydrogen, unconverted carbon monoxide, carbon dioxide, nitrogen, C 1 -C 2 hydrocarbons, and C 3 + hydrocarbons. As it is derived from the Fischer-Tropsch process it generally is at a temperature of in the range of 40-100 °C, more in particular in the range of 50-70 °C and at a pressure of 40-80 bar, more in particular in the range of 50-70 bar.
  • Suitable pretreatment steps include removal of hydrogen and/or carbon dioxide.
  • the gas as it enters the process according to the invention generally is at a temperature in the range of 20-150 °C, in particular 40-100 °C, more in particular in the range of 50-70 °C and at a pressure of 15-80 bar, in particular 40-80 bar, more in particular in the range of 50-70 bar.
  • the Fischer-Tropsch off-gas as it enters the process according to the invention comprises carbon monoxide, nitrogen, C 1 -C 2 hydrocarbons, and C 3 + hydrocarbons.
  • the C 3 + hydrocarbons are present in an amount of at least 0.5 mol%, more in particular in an amount of at least 0.8 mol%.
  • the C3+ hydrocarbons are present in an amount up to 5 mol%, more in particular in an amount up to 4 mol%.
  • the C 3 + hydrocarbons are C 3 -C 6 saturated and unsaturated hydrocarbons.
  • the word hydrocarbons also encompasses oxygenates, such as alcohols.
  • the Fischer-Tropsch off-gas is provided to an expander.
  • an expander a high-pressure gas is expanded while producing work.
  • the work is used to generate power in a generator.
  • Expanders are known in the art. They are used, e.g., as sources of refrigeration in industrial processes such as the extraction of ethane and natural gas liquids (NGLs) from natural gas, the liquefaction of gases (and other low-temperature processes by driving a compressor.
  • a well known expander is a turboexpander, also referred to as a turbo-expander or an expansion turbine. It is a centrifugal or axial flow turbine through which a high pressure gas is expanded to produce work that is often used to drive a compressor. It is within the scope of the skilled person to select and apply a suitable expander.
  • Another suitable type of expander is a twister, also known in the art.
  • the gas cools down to a point in temperature and pressure which is below the condensation point of the C 3 + fraction in the composition, and a liquid condensate is formed which comprises the C 3 + fraction.
  • the process is controlled by the desired end pressure to be achieved in the expander, which is in turn controlled by the desired down-stream processing for the gaseous product stream coming from the expander.
  • the temperature attained in the expander is a function of the starting temperature of the off-gas as it enters the expander and the pressure reduction achieved in the expander.
  • the pressure of the gas as it leaves the expander is at least a factor of 2 lower than the pressure of the gas as it enters the expander.
  • the pressure of the gas as it leaves the expander may be a factor 2.5 lower than the pressure of the gas as it enters the expander, or a factor of 3 lower.
  • the gas as it leaves the expander prefferably be at a pressure in the range of 1-10 bar, in particular 3-8 bar.
  • the temperature of the gas is reduced to a value in the range of -100 to - 20 °C.
  • the generation of low-temperature cold by the expander is an additional advantage of the process according to the invention. For example, it can be used too cool process streams of processes carried out in the vicinity of the process according to the invention.
  • the gas as it enters the expander is at a temperature in the range of 20-150 °C, in particular 40-100 °C, more in particular in the range of 50-70 °C and at a pressure in the range of 15-80 bar, in particular 40-80 bar, more in particular in the range of 50-70 bar and the gas as it leaves the expander is at a temperature in the range -100 to -20 °C, more in particular in the range of -80 to -40 °C and at a pressure in the range of 1-10 bar, more in particular in the range of 3-8 bar.
  • the gas as it enters the expander is at a temperature in the range of 20-150 °C, in particular 20-80 °C, more in particular in the range of 40-60°C and at a pressure in the range of 15-45 bar, more in particular in the range of 20-38 bar and the gas as it leaves the expander is at a temperature in the range -100 to -20 °C, more in particular in the range of -70 to -30 °C and at a pressure in the range of 1-10 bar, more in particular in the range of 3-8 bar.
  • the gas as it enters the expander is at a temperature in the range of 100-150 °C, more in particular in the range of 110-130 °C and at a pressure in the range of 40-80 bar, more in particular in the range of 50-70 bar and the gas as it leaves the expander is at a temperature in the range -60 to -10 °C, more in particular in the range of -40 to -20 °C and at a pressure in the range of 1-10 bar, more in particular in the range of 3-8 bar.
  • the gas as it enters the expander is at a temperature in the range of 50-90 °C, more in particular in the range of 60-80 °C and at a pressure in the range of 15-45 bar, more in particular in the range of 20-38 bar and the gas as it leaves the expander is at a temperature in the range -60 to -10 °C, more in particular in the range of -45 to -25 °C and at a pressure in the range of 1-10 bar, more in particular in the range of 3-8 bar.
  • liquid condensate is formed.
  • the amount and composition of the condensate formed depends on the composition of the Fischer-Tropsch off-gas and on the conditions at which the expander is operated.
  • the process according to the invention aims at forming a condensate comprising a substantial amount of C 3 + hydrocarbons.
  • the condensate contains more than 50 wt% of C 3 + hydrocarbons, in particular more than 70 wt% of C 3 + hydrocarbons, still more in particular more than 80 wt% of C 3 + hydrocarbons, still more in particular more than 90 wt%, calculated on the total weight of the condensate formed.
  • the condensate may also contain one or more of C 2 hydrocarbons, C 1 hydrocarbons, and carbon dioxide.
  • the condensate is withdrawn from the expander. It may, optionally after removal of carbon dioxide, be processed further by combining it with the liquid effluent from the Fischer-Tropsch reactor, or by combining it with other refinery steams with a comparable composition.
  • the condensate contains a substantial amount of C 3 + hydrocarbons as specified above, in particular where it contains more than 70 wt% of C 3 + hydrocarbons, more than 80 wt% of C 3 + hydrocarbons, or even more than 90 wt% of C 3 + hydrocarbons
  • the condensate can, for example, be processed by combining it with other hydrocarbon streams with the same composition
  • the condensate is provided to the LPG pool.
  • the condensate contains less than 50 wt% of C 3 + hydrocarbons, it may be necessary to subject the condensate to a separation step to separate the C 3 + fraction from the lower-boiling components.
  • the C 3 + fraction can then be processed as described above.
  • the condensate may contain water.
  • an expander is used to remove water from the gas stream while generating energy.
  • the gaseous effluent is also withdrawn from the expander. It may be processed in a number of different ways.
  • the gaseous effluent from the expander is fed through a heat exchanger. Feeding the effluent to a heat exchanger is advantageous for two reasons. In the first place, it allows heating of the gaseous effluent to a temperature in a range suitable for further processing. At the same time, it can be used to cool down other streams.
  • the gas as it leaves the expander is at a pressure of 1-10 bar, in particular 3-8 bar, and is provided to a heat exchanger, where the temperature of the gas is increased to a value in the range of 25-60 °C, in particular to a value in the range of 40-50 °C.
  • the process according to the invention comprises the step of splitting the Fischer-Tropsch off-gas stream into at least two streams, wherein a first stream is brought to a pressure in the range of 1-10 bar, in particular 3-8 bar, and a temperature in the range of 25-60 °C, in particular in the range of 40-50 °C, and a second stream is brought to a pressure in the range of 10-50 bar, in particular 20-40 bar, and a temperature in the range of 25-100 °C.
  • This embodiment allows the production of both high-pressure fuel gas and low-pressure fuel gas.
  • high-pressure fuel gas is gas at a pressure in the range of more than 10 bar to 50 bar, more in particular in the range of 20-40 bar, and a temperature in the range of 25-100 °C.
  • the temperature is 26-60 °C, in particular 40-50 °C.
  • the temperature is 50-100 °C, in particular 60-80 °C.
  • the gas generally is at a temperature at least 20 °C above its saturation temperature.
  • low-pressure fuel gas is gas at a pressure of 1-10 bar, in particular 3-8 bar, and a where the temperature of the gas is increased to a value in the range of 25-60 °C, in particular to a value in the range of 40-50 °C.
  • the gas generally is at a temperature at least 20 °C above its saturation temperature.
  • HPFG may, for example, be provided to a gas turbine generator (GTG).
  • GTG gas turbine generator
  • LPFG may, for example, be provided to a furnace and/or boiler, e.g., a steam-methane reformer furnace (SMR), or a high-pressure steam boiler combined with a superheater.
  • SMR steam-methane reformer furnace
  • the Fischer-Tropsch off-gas stream is divided into two streams, wherein one stream is subjected to an expansion step in an expander unit to a temperature and pressure which is such that the gas is below it condensation point, resulting in the formation of liquid condensate.
  • the Fischer-Tropsch off-gas is provided to a pre-heater before being provided to the expansion step.
  • a pre-heater By increasing the temperature of the Fischer-Tropsch step before the expansion step, more energy will be generated in the expansion step.
  • the heat provided in the pre-heater may be low-level heat generated by other processes at the location where the process according to the invention is carried out.
  • the temperature of the gas is increased to a value in the range of 101-150 °C, in particular 110-140 °C.
  • expanders may also be incorporated which do not generate condensate.
  • There expanders can, for example, be used to decrease the pressure of the Fischer-Tropsch off-gas to a value of more than 10 to 50 bar, in particular to 20-40 bar.
  • the temperature of the expanded gas may be in the range of 0-80 °C. If so desired, the thus expanded gas may be provided to a heat-exchanger where it is heated to a temperature which makes it suitable for use as HPFG.
  • a Fischer-Tropsch off-gas is provided through line 1 to an expander 2.
  • expander 2 the gas expands while generating energy.
  • the expander is coupled to a generator (not shown).
  • the effluent from the expander is fed to a heat exchanger 4, where its temperature is increased.
  • the effluent from the heat exchanger, which is HPFG is withdrawn through line 5.
  • Part of the effluent say, between 10 and 90 vol%, in particular between 30 and 70 vol%, is separated off through line 7, depressurised in valve 9, to form LPFG which may be processed in processing unit 10, which is a furnace and/or boiler, for example a SMR or a high-pressure steam boiler combined with a superheater.
  • processing unit 6 which is, for example, a GTG.
  • Table 1 temperatures and pressures of gas streams in Figure 1.
  • general T (°C) pref. T (°C) FT off gas (1) 20-80 40-80 20-150 40-100 50-70 50-70 expanded gas (3) 10-50 20-40 0-20 5-15 heat-exchanged gas (HPFG) (5) 10-50 20-40 25-60 40-50 depressurised gas (LPFG) (9) 1-10 3-8 25-60 40-50
  • the temperature attained in expander 2 is too high for a condensate to be formed. This process is thus not in accordance with the present invention.
  • Figure 2 illustrates one embodiment of a process according to the invention.
  • Fischer-Tropsch off-gas is provided through line 1.
  • Part of the gas say, between 10 and 90 vol%, in particular between 30 and 70 vol%, is separated off through line 11.
  • the remainder of the Fischer-Tropsch off-gas is provided to an expander 2.
  • expander 2 the gas expands while generating energy.
  • the expander is coupled to a generator (not shown).
  • the effluent from the expander is fed to a heat exchanger 4, where its temperature is increased.
  • the effluent from the heat exchanger, which is HPFG is withdrawn through line 5 and fed to processing unit 6, which is, for example, a GTG.
  • the part of the Fischer-Tropsch off-gas withdrawn through line 11 is fed to an expander 12.
  • expander 12 the gas expands while generating energy.
  • the expander is coupled to a generator (not shown). This generator may be the same as the generator connected to expander 2, or a separate generator may be provided.
  • a liquid condensate is formed, which is withdrawn through line 14.
  • the gaseous effluent from the expander is withdrawn through line 13 and fed to a heat exchanger 15, where its temperature is increased.
  • the effluent from the heat exchanger 15, which is LPFG may provided through line 16 to processing unit 10, which is a furnace and/or boiler, for example a SMR or a high-pressure steam boiler combined with a superheater.
  • Table 2 temperatures and pressures of gas streams in Figure 2.
  • liquid condensate is formed in expander 12 but not in expander 2.
  • expander 2 and heat exchanger 4 are replaced with a valve, where the gas is depressurised to form HPFG, which is then provided to processing unit 6, which is, for example, a GTG.
  • FIG. 3 illustrates a further embodiment of the present invention.
  • a Fischer-Tropsch off-gas is provided through line 1 to an expander 2.
  • expander 2 the gas expands while generating energy.
  • the expander is coupled to a generator (not shown).
  • the effluent from the expander is fed to a heat exchanger 4, where its temperature is increased.
  • the effluent from the heat exchanger, which is HPFG is withdrawn through line 5.
  • Part of the effluent say, between 10 and 90 vol%, in particular between 30 and 70 vol%, is separated off through line 7.
  • the remainder of the HPFG in line 5 is fed to processing unit 6, which is, for example, a GTG.
  • the part of the Fischer-Tropsch off-gas withdrawn through line 7 is fed to an expander 17.
  • expander 17 the gas expands while generating energy.
  • the expander is coupled to a generator (not shown). This generator may be the same as the generator connected to expander 2, or a separate generator may be provided.
  • a liquid condensate is formed, which is withdrawn through line 18.
  • the gaseous effluent from expander 17 is withdrawn through line 19 and fed to a heat exchanger 20, where its temperature is increased.
  • the effluent from the heat exchanger 20, which is LPFG may provided through line 21 to processing unit 10, which is a furnace and/or boiler, for example a SMR or a high-pressure steam boiler combined with a superheater.
  • Table 3 temperatures and pressures of gas streams in Figure 3.
  • liquid condensate is formed in expander 17 but not in expander 2.
  • additional heat is provided to the gas before in is fed to the expander. This allows the conversion of low-level waste heat to energy. For example, it may be attractive to pre-heat the Fischer-Tropsch off gas from a temperature in the range of 40-100 °C, in particular 50-70 °C, to a temperature in the range of 101-150 °C, in particular in the range of 110-140 °C.
  • This embodiment can be integrated in the process according to the invention in a number of ways. A few of these are elucidated in figures 4-6 .
  • FIG. 4 illustrates a further embodiment of a process according to the invention.
  • Fischer-Tropsch off-gas is provided through line 1.
  • Part of the gas say, between 10 and 90 vol%, in particular between 30 and 70 vol%, is separated off through line 24.
  • the remainder of the Fischer-Tropsch off-gas is provided to valve 22, where it depressurised and cooled down.
  • the effluent from valve 22, which is HPFG, may provided through line 16 to processing unit 6, which is, for example, a GTG.
  • the part of the Fischer-Tropsch off-gas withdrawn through line 24 is fed to a pre-heater 25, where the temperature of the gas is increased.
  • the effluent from the pre-heater 25 is provided through line 26 to an expander 27.
  • expander 27 the gas expands while generating energy.
  • the expander is coupled to a generator (not shown).
  • a liquid condensate is formed, which is withdrawn through line 28.
  • the gaseous effluent from the expander is withdrawn through line 29 and fed to a heat exchanger 30, where its temperature is increased.
  • the effluent from heat exchanger 30, which is LPFG is withdrawn through line 31 and fed to processing unit 10, which is a furnace and/or boiler, for example a SMR or a high-pressure steam boiler combined with a superheater.
  • Table 4 temperatures and pressures of gas streams in Figure 4.
  • liquid condensate is formed in expander 27.
  • pre-heater 25 makes for an increased amount of energy generated in expander 27.
  • Fischer-Tropsch off-gas is provided through line 1. It is fed to pre-heater 32, where its temperature is increased. The effluent from pre-heater 32 is withdrawn through line 33. Part of the gas, say, between 10 and 90 vol%, in particular between 30 and 70 vol%, is separated off through line 36. The remainder of the gas is provided to expander 34. In expander 34, the gas expands while generating energy. The expander is coupled to a generator (not shown). The effluent from expander 34, which is HPFG, is withdrawn through line 35 and fed to processing unit 6, which is, for example, a GTG. The part of the gas withdrawn through line 36 is fed to an expander 37.
  • processing unit 6 which is, for example, a GTG.
  • expander 37 the gas expands while generating energy.
  • the expander is coupled to a generator (not shown). This generator may be the same as the generator connected to expander 34, or a separate generator may be provided.
  • a liquid condensate is formed, which is withdrawn through line 38.
  • the gaseous effluent from the expander is withdrawn through line 39 and fed to a heat exchanger 40, where its temperature is increased.
  • the effluent from the heat exchanger 40 which is LPFG, may provided through line 41 to processing unit 10, which is a furnace and/or boiler, for example a SMR or a high-pressure steam boiler combined with a superheater.
  • Table 5 temperatures and pressures of gas streams in Figure 5.
  • liquid condensate is formed in expander 37 but not in expander 34.
  • FIG. 6 A further embodiment of the present invention where a pre-heater is used in combination with an expander is illustrated in Figure 6 .
  • Fischer-Tropsch off-gas is provided through line 1. It is fed to pre-heater 32, where its temperature is increased. The effluent from pre-heater 32 is withdrawn through line 33, and led to expander 42. In expander 42, the gas expands while generating energy. The expander is coupled to a generator (not shown). The effluent from expander 42 is withdrawn through line 43. Part of the gas, say, between 10 and 90 vol%, in particular between 30 and 70 vol%, is separated off through line 44. The remainder of the gas, which is HPFG is fed to processing unit 6, which is, for example, a GTG.
  • processing unit 6 which is, for example, a GTG.
  • the part of the gas withdrawn through line 44 is fed to an expander 45.
  • expander 45 the gas expands while generating energy.
  • the expander is coupled to a generator (not shown). This generator may be the same as the generator connected to expander 42, or a separate generator may be provided.
  • a liquid condensate is formed, which is withdrawn through line 46.
  • the gaseous effluent from the expander is withdrawn through line 47 and fed to a heat exchanger 48, where its temperature is increased.
  • the effluent from the heat exchanger 48 which is LPFG, may provided through line 49 to processing unit 10, which is a furnace and/or boiler, for example a SMR or a high-pressure steam boiler combined with a superheater.
  • Table 6 temperatures and pressures of gas streams in Figure 6.
  • liquid condensate is formed in expander 45 but not in expander 42.

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)
  • Separation By Low-Temperature Treatments (AREA)
EP09161901A 2009-06-04 2009-06-04 Procédé de traitement d'un dégagement gazeux Fischer-Tropsch Withdrawn EP2258814A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP09161901A EP2258814A1 (fr) 2009-06-04 2009-06-04 Procédé de traitement d'un dégagement gazeux Fischer-Tropsch

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP09161901A EP2258814A1 (fr) 2009-06-04 2009-06-04 Procédé de traitement d'un dégagement gazeux Fischer-Tropsch

Publications (1)

Publication Number Publication Date
EP2258814A1 true EP2258814A1 (fr) 2010-12-08

Family

ID=41203914

Family Applications (1)

Application Number Title Priority Date Filing Date
EP09161901A Withdrawn EP2258814A1 (fr) 2009-06-04 2009-06-04 Procédé de traitement d'un dégagement gazeux Fischer-Tropsch

Country Status (1)

Country Link
EP (1) EP2258814A1 (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102013226126A1 (de) * 2013-12-16 2015-06-18 Technische Universität Bergakademie Freiberg Allotherme Methan-Reformierung mit physikalischer Energierückgewinnung
JP2021045749A (ja) * 2015-11-17 2021-03-25 ダウ グローバル テクノロジーズ エルエルシー 工業的プロセスからのco2排出を減少する方法とシステム

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL7413678A (en) 1974-10-18 1976-04-21 Shell Int Research Hydrocarbons from carbonaceous fuels - by partial combustion and catalytic reaction of carbon monoxide and hydrogen
WO1999015483A1 (fr) 1997-09-25 1999-04-01 Shell Internationale Research Maatschappij B.V. Procede de production d'hydrocarbures liquides
EP1004561A1 (fr) 1998-11-27 2000-05-31 Shell Internationale Researchmaatschappij B.V. Procédé pour la préparation d'hydrocarbures liquides
WO2005019384A1 (fr) * 2003-08-22 2005-03-03 Sasol Technology (Proprietary) Limited Procede de synthese d'hydrocarbures
WO2006033025A1 (fr) * 2004-02-05 2006-03-30 Sasol Technology (Proprietary) Limited Synthese d'hydrocarbures
WO2006120223A1 (fr) * 2005-05-13 2006-11-16 Shell Internationale Research Maatschappij B.V. Elimination de dioxyde de carbone d'un flux gazeux
US20090124713A1 (en) * 2006-11-08 2009-05-14 Canada Chemical Corporation Low-pressure Fischer-Tropsch process

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL7413678A (en) 1974-10-18 1976-04-21 Shell Int Research Hydrocarbons from carbonaceous fuels - by partial combustion and catalytic reaction of carbon monoxide and hydrogen
WO1999015483A1 (fr) 1997-09-25 1999-04-01 Shell Internationale Research Maatschappij B.V. Procede de production d'hydrocarbures liquides
EP1004561A1 (fr) 1998-11-27 2000-05-31 Shell Internationale Researchmaatschappij B.V. Procédé pour la préparation d'hydrocarbures liquides
WO2005019384A1 (fr) * 2003-08-22 2005-03-03 Sasol Technology (Proprietary) Limited Procede de synthese d'hydrocarbures
WO2006033025A1 (fr) * 2004-02-05 2006-03-30 Sasol Technology (Proprietary) Limited Synthese d'hydrocarbures
WO2006120223A1 (fr) * 2005-05-13 2006-11-16 Shell Internationale Research Maatschappij B.V. Elimination de dioxyde de carbone d'un flux gazeux
US20090124713A1 (en) * 2006-11-08 2009-05-14 Canada Chemical Corporation Low-pressure Fischer-Tropsch process

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102013226126A1 (de) * 2013-12-16 2015-06-18 Technische Universität Bergakademie Freiberg Allotherme Methan-Reformierung mit physikalischer Energierückgewinnung
JP2021045749A (ja) * 2015-11-17 2021-03-25 ダウ グローバル テクノロジーズ エルエルシー 工業的プロセスからのco2排出を減少する方法とシステム
JP2022066275A (ja) * 2015-11-17 2022-04-28 ダウ グローバル テクノロジーズ エルエルシー 工業的プロセスからのco2排出を減少する方法とシステム

Similar Documents

Publication Publication Date Title
JP2516851B2 (ja) 一貫式ガス化組合せサイクル電力発生方法
EP1465834B1 (fr) Procede de production d'hydrocarbures
EA006062B1 (ru) Способ переработки природного газа в жидкие продукты
US20080087863A1 (en) Process for co-production of electricity and hydrogen-rich gas vapor reforming of a hydrocarbon fraction with input of calories by combustion with hydrogen in situ
CN102427868A (zh) 从合成气或烟道气中分离co2的方法和系统
US20220298965A1 (en) Systems and methods for oxidation of hydrocarbon gases
RU2648914C2 (ru) Способ получения водорода и генерирования энергии
US8901178B2 (en) Co-production of fuels, chemicals and electric power using turbochargers
US8268896B2 (en) Co-production of fuels, chemicals and electric power using gas turbines
CA2856802C (fr) Traitement de produits en provenance d'un puits de petrole
EP2258814A1 (fr) Procédé de traitement d'un dégagement gazeux Fischer-Tropsch
CA2620734C (fr) Procede de production d'un flux d'hydrocarbure a partir d'une zone souterraine
US4209305A (en) Process for making substitute natural gas
EP2531442B1 (fr) Séparation de gaz
US10836634B1 (en) Integrated GTL process
GB2493400A (en) Separation of carbon dioxide and hydrogen
EP2256317A1 (fr) Procédé pour produire de l'énergie
US20230249968A1 (en) Conversion of a hydrocarbon feed gas to synthesis gas for producing hydrocarbons
GB1573401A (en) Making substitute natural gas
CN101873990A (zh) 制造冷却的压缩合成气的方法和设备
TH71291B (th) วิธีการและอุปกรณ์สำหรับการได้ผลิตผลก๊าซและมีเทนเหลวจากก๊าซสังเคราะห์
TH101024A (th) วิธีการและอุปกรณ์สำหรับการได้ผลิตผลก๊าซและมีเทนเหลวจากก๊าซสังเคราะห์

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO SE SI SK TR

RIN1 Information on inventor provided before grant (corrected)

Inventor name: WEE CHELSIA HSIA

Inventor name: ZHAO YING

Inventor name: SCHOLTEN R.J

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20110609