US3818714A - Process for the liquefaction and subcooling of natural gas - Google Patents
Process for the liquefaction and subcooling of natural gas Download PDFInfo
- Publication number
- US3818714A US3818714A US00231984A US23198472A US3818714A US 3818714 A US3818714 A US 3818714A US 00231984 A US00231984 A US 00231984A US 23198472 A US23198472 A US 23198472A US 3818714 A US3818714 A US 3818714A
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- US
- United States
- Prior art keywords
- cycle
- gas
- liquid
- nitrogen
- precooling
- 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.)
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- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 title claims abstract description 134
- 238000000034 method Methods 0.000 title claims abstract description 38
- 239000003345 natural gas Substances 0.000 title claims abstract description 29
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 107
- 239000007789 gas Substances 0.000 claims abstract description 60
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 54
- 239000000203 mixture Substances 0.000 claims abstract description 25
- 239000007788 liquid Substances 0.000 claims description 48
- 238000009835 boiling Methods 0.000 claims description 26
- 238000001704 evaporation Methods 0.000 claims description 21
- 238000005057 refrigeration Methods 0.000 claims description 17
- 230000008020 evaporation Effects 0.000 claims description 15
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 claims description 14
- 229930195733 hydrocarbon Natural products 0.000 claims description 11
- 150000002430 hydrocarbons Chemical class 0.000 claims description 11
- 230000005494 condensation Effects 0.000 claims description 6
- 238000009833 condensation Methods 0.000 claims description 6
- LWSYSCQGRROTHV-UHFFFAOYSA-N ethane;propane Chemical compound CC.CCC LWSYSCQGRROTHV-UHFFFAOYSA-N 0.000 claims description 2
- 238000001816 cooling Methods 0.000 abstract description 9
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 32
- 239000001294 propane Substances 0.000 description 16
- 230000000694 effects Effects 0.000 description 8
- 239000007792 gaseous phase Substances 0.000 description 6
- 239000003949 liquefied natural gas Substances 0.000 description 5
- 238000000926 separation method Methods 0.000 description 5
- 230000003247 decreasing effect Effects 0.000 description 3
- 239000007791 liquid phase Substances 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- JVFDADFMKQKAHW-UHFFFAOYSA-N C.[N] Chemical compound C.[N] JVFDADFMKQKAHW-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 239000003507 refrigerant Substances 0.000 description 2
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 238000010588 boiling point diagram Methods 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 230000000153 supplemental effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910001868 water Inorganic materials 0.000 description 1
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- 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
- F25J3/02—Processes 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
- F25J3/0228—Processes 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
- F25J3/0257—Processes 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
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- F25J1/00—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures
- F25J1/0002—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures characterised by the fluid to be liquefied
- F25J1/0022—Hydrocarbons, e.g. natural gas
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- 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
- F25J2220/00—Processes or apparatus involving steps for the removal of impurities
- F25J2220/60—Separating impurities from natural gas, e.g. mercury, cyclic hydrocarbons
- F25J2220/64—Separating heavy hydrocarbons, e.g. NGL, LPG, C4+ hydrocarbons or heavy condensates in general
-
- 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
- F25J2245/00—Processes or apparatus involving steps for recycling of process streams
- F25J2245/02—Recycle of a stream in general, e.g. a by-pass stream
-
- 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
- F25J2290/00—Other details not covered by groups F25J2200/00 - F25J2280/00
- F25J2290/10—Mathematical formulae, modeling, plot or curves; Design methods
Definitions
- ABSTRACT A process for the liquefaction and subcooling of natural gas with a Claude closed refrigerating cycle comprising compressing gaseous cycle medium; cooling resultant compressed-gaseous cycle medium; dividing cooled compressed gas into two streams; engineexpanding one stream; and cooling the other stream with the engine-expanded stream to such an extent that said other stream becomes partially liquefied after a subsequent throttle expansion thereof; the improvement comprising employing as the cycle medium, a
- This invention relates to a process for liquefaction and subcooling of natural gas by a Claude cycle.
- This cycle comprises compressing cycle gas; cooling same; dividing cooled compressed gas into two streams; engine-expanding one stream; and cooling the other stream with the engine-expanded stream to such an extent that said other stream becomes partially liquefied after a subsequent throttle expansion thereof.
- peak cold is made available, namely that amount of refrigeration required for subcooling the natural gas.
- the natural gas Before subcooling, the natural gas has already been liquefied under a higher pressure by heat exchange with the cycle gas, but the subcooling ensures that the natural gas remains practically entirely in the liquid phase even after expansion to the pressure of the storage tank. If it is desired to avoid operation of the Claude cycle under a negative pressure, it is essential to employ as the cycle medium a gas having a lower boiling point than methane, nitrogen being conventionally employed.
- FIG. 1 is a boiling point-composition diagram for N -CH at various pressures.
- FIGS. 2 and 3 are schematic views of preferred embodiments of the process.
- the methane in mixture with the nitrogen, is vaporized at its partial pressure, i.e., a pressure lower than the ambient evaporation pressure, it is possible to obtain, with methane, a specific low temperature at a relatively high pressure level.
- the refrigerating capacity of the Claude cycle is likewise improved by the addition of methane to the nitrogen.
- methane as a less than ideal gas, increases the Joule-Thomson effect in the peak cooler, so that the amount of cycle gas to be fed to the J-T valve can be smaller, and a larger proportion of the cycle gas can be fed to the engine expansion.
- the enthalpy gradient in the turbine and thus the specific refrigerating capacity of the cycle, based on the unit quantity of circulated gas is larger in the case of methane than in the case of nitrogen. The same holds true for the isothermal Joule-Thomson effect at the warm end. Therefore, in total, the amount of cycle gas required to produce a specific amount of cold is reduced.
- the use of a methane-nitrogen mixture as the cycle gas affords the further advantage that the leakage losses of the cycle medium can be compensated for at less cost by utilizing natural gas therefor. This is so because the separation of a gas rich in nitrogen prior to the liquefaction is in most cases absolutely necessary, even in case of gases of low nitrogen content, since too great a drop in the liquefaction temperature of the natural gas must be avoided.
- the above-described advantage is especially noticeable in the processing of natural gases having a low nitrogen content, for otherwise rectification devices would have to be provided in this pro cedure wherein the nitrogen is separated from the natural gas not only in a high purity, but also in good yields.
- the process according to the present invention offers advantages even if the natural gas contains no nitrogen at all, since only that proportion of the leakage losses associated with the nitrogen need be made up from a source externally of the plant, whereas the lost methane can readily be taken from the natural gas.
- the nitrogen concentration of the cycle gas is, on a molar basis, at least 20 percent, preferably at least 40 percent, conversely, the maximum preferred nitrogen concentration is 80 percent, particularly 60 percent.
- a nitrogen separation unit is incorporated in the natural gas liquefaction process. From the head of this unit there is withdrawn a fraction having a nitrogen concentration of at least the same level as that of the cycle gas, and this fraction is then fed into the cycle as makeup gas. If this fraction contains more nitrogen than the cycle gas, then supplemental methane from the purified natural gas (freed of CO H 0, and heavy hydrocarbons) can be added thereto.
- One negative feature of the cycle of this invention is that the cycle gas must be precooled to a very low temperature prior to entering the expansion engine so that it can be cooled to a sufficiently low temperature during the expansion.
- This precooling can be conducted conventionally with a multistage refrigerating machine operating with freon, ammonia, or propane, also including, in many cases, an essential third stage of vacuum.
- These refrigerating machines exhibit the same disadvantage described above in connection with the Claude cycle, namely that the refrigeration is transferred at a constant temperature, to a stream having a sliding temperature.
- there is employed a mixture of methane, propane, and optionally ethane as the cycle medium for the precooling cycle is employed.
- a main advantage of this latter feature is that the refrigeration liberated during the evaporation is transferred at a decreasing temperature so that small temperature differences (ATs) can be employed in the heat exchangers, resalting in a thermodynamically more efficient process. Since the propane and any ethane present evaporate under a partial pressure lower than the total pressure ambient during the evaporation, the desired low temperature is obtained at a higher total pressure than would be the case when evaporating pure ethane or propane. In other words, because the transfer of peak cold involves a smaller pressure drop, the number of compressor stages and thus the number of evaporators is decreased, and the cost of control elements is also reduced.
- leakage losses amounting to about 1 5 parts per thousand of the quantity of cycle medium can frequently be covered, in the case of methane and ethane, merely by simple separation from the natural gas proper, i.e., they need not be stored in additional tanks. Propane is always available in any case so that the BTU value of the gas can be adjusted or desired.
- the proportion of each of methane, propane and optionally ethane in the total of the cycle gas is about 20-50 molar percent, respectively.
- a cycle gas having a composition, of in moles percent 40 and 60 methane; 25 and 60 percent propane; and 0 and 15 ethane.
- the precooling temperature attainable in this manner is generally sufficient, even in case of low natural gas pressures, to result in the condensation of the heavy hydrocarbons which, otherwise, could lead to obstructions in the low-temperature sections.
- the plant can be rapidly brought to the required cold operating condition.
- an even lower precooling temperature e.g. to 200 K
- a fraction of the cycle medium remains in the gaseous phase downstream of the final cooler of the compressor, and the fraction containing lower boiling components is separated from the liquid fraction containing predominantly the higher-boiling hydrocarbons.
- Both separated gas and liquid are then cooled by heat exchange with the liquid evaporating at the suction pressure of the compressor.
- the gas rich in lower-boiling components is thus totally condensed, and is then in the liquid phase expanded (pressurereduced) to the suction pressure of the compressor.
- the resultant liquid is then evaporated to effect said total condensation.
- the natural gas to be processed (0.6,780 Nm /hr.), after having been freed of water, carbon dioxide, and hydrogen sulfide, and having approximately the following composition: 2 percent nitrogen, 94 percent methane, 3 percent ethane, l percent propane and higher hydrocarbons, is fed to the plant, via conduit 1, at 298 K and under 39 ata. and is then cooled in the heat exchanger 2 to 216 K. During this step, the C and higher hydrocarbons are substantially condensed, which would otherwise cause clogging in subsequent sections of the plant.
- phase separator 3 evaporated and warmed in heat exchanger 2
- discharged from the plant via conduit 4 The portion remaining in the gaseous phase is further cooled in heat exchanger 5 to about 190 K; during this step, a liquid is obtained consisting of about 85 percent methane, percent ethane, and 5 percent propane.
- This liquid after being passed in separator-collector 6, is branched into two streams, and the amount necessary to make up for leakage losses of the precooling cycle is introduced into the latter via conduit 7.
- the remainder is evaporated and warmed in heat exchangers 5 and 2, and then discharged from the plant via conduit 4.
- a portion of the gas withdrawn from the separator 6 overhead is now further cooled in the heat exchanger 8 to 163 K and expanded into the nitrogen separation column 9 operating at 22 ata.
- the remaining gas is conducted through a heating coil located in the sump of the column 9 and is then expanded into the midsection of column 9.
- a temperature of about 150 K is maintained; the gaseous head product consists of 50 percent of a methane and 50% of nitrogen.
- This head product is discharged from the plant via conduit 4, except for that amount of gas required for providing makeup due to the leakage losses of the Claude refrigerating cycle and which is fed into said cycle via conduit 10. From the sump of the column 9, 5,820 Nm /h.
- liquid natural gas is withdrawn having a temperature of 167 K and approximately the following composition: 97 percent methane, 1 percent nitrogen, and 2 percent ethane.
- This liquid is passed to the heat exchangers l1 and 12 and cooled therein to l 1 1 K so that, during the subsequent expansion in the valve 13 to the pressure of the storage tank (slightly above 1 ata.), only a minimum amount of liquid is evaporated (about 40 Nm lh).
- the refrigeration required for the liquefaction is provided by a Claude cycle with precooling by a one-stage cycle based on a mixture of gases.
- This mixture comprises 50 percent methane and 50 percent nitrogen and is employed as the cycle medium.
- This gas (37,900 Nm lhr) is compressed, in compressor 14, to 25.5 ata., and after being cooled, is further compressed to 35.5 ata. in compressor 15.
- the gas enters the heat exchanger 2 at a temperature of 298 K and is precoolcd therein and also in the heat exchanger 5 to 197 K.
- cycle gas 35,600 Nm /h. of cycle gas is then expanded in the expansion turbine 16 to 8 ata. and, during this step, is cooled to 138 K.
- a portion of this gas is branched off via conduit 17 and serves for cooling the head of column 9; the main quantity is fed, via conduit 18, to the cold end of the heat exchanger 11, heated therein and in heat exchangers 8, 5, and 2, to ambient temperature and thereafter recompressed in the compressor 14.
- the proportion of the cycle medium not subjected to engine expansion i.e., 2,300 Nm /h., is cooled in conduit 19 under its pressure of 35.5 ata. in heat exchangers 8, l1, and 12, to 111 K.
- the temperature drops to 109 K, so that the liquid natural gas can be subcooled to l 1 1 K by heat exchange with the boiling cycle liquid, before it is expanded in valve 13.
- the throttle-expanded cycle medium is combined with the engine-expanded cycle medium, and is warmed and recompressed together therewith.
- the cycle medium of the precooling cycle consists of 45 percent methane, 5 percent ethane, and 50 percent propane. 4,200 Nm lh. of this gas is compressed in compressor 22 from 10 ata. to 50 ata., cooled and simultaneously liquefied in heat exchanger 2, and then expanded to 10 ata. in valve 23.
- the precooling temperature attainable in this manner i.e., the temperature at which the gaseous streams to be cooled leave the cold end of the heat exchanger 2, is 216 K.
- the evaporated and warmed cycle medium is then recompressed in the compressor 22.
- the leakage losses of the cycle as mentioned above, are, in part, compensated for by the liquid withdrawn from separator 6 via conduit 7.
- this liquid contains less propane than the cycle medium, pure propane or a gas more enriched therewith must be added. This can be done by conducting the gaseous stream returning to the compressor 22 via conduit 30 through the tank 28 filled with liquid propane, rather than via conduit 29.
- the dome 31 serves as an entrainment separator for the separation of droplets of liquid propane.
- the cycle medium consists of about percent methane, 5 percent ethane, and 25 propane.
- the liquid formed in the secondary cooler of the compressor denoted by 24 is separated from the gaseous phase in the separator 25, cooled in heat exchanger 2, expanded in valve 23' from 35 to 8 ata., and reevaporated and warmed in heat exchanger 2.
- the gaseous phase enriched in the lower-boiling components of the cycle medium is withdrawn from separator 25, conducted, via conduit 26, through the heat exchangers 2 and 5, being cooled and liquefied during this step, and then expanded in valve 27 from 35 to 8 ata.
- a precooling temperature of about K is attacined at the cold end of the heat exchanger 5.
- the cycle medium evaporated and warmed in heat exchanger 5 is recombined with the cycle medium expanded in valve 23', and the combined stream is then recycled to the suction side of compressor 22.
- B in FIG. 3 denotes the sum total of the remaining gaseous streams to be cooled, i.e., the natural gas to be liquefied and the compressed cycle medium of the Claude cycle; and C denotes the sum total of the other gaseous streams to be warmed, i.e., the fractions obtained during the natural gas liquefaction and to be discharged from the plant in the gaseous phase, and the expanded cycle medium of the Claude cycle.
- the improvement comprising employing as the cycle medium, a mixture of nitrogen and methane.
- a process according to claim 1, wherein the nitrogen molar concentration in the cycle medium is at least 40 percent.
- a process according to claim 1 further comprising separating the natural gas from CO H and heavy hydrocarbons; separating a nitrogen enriched stream from resultant purified natural gas, the nitrogen content of said enriched stream being at least as large as that of said cycle medium and feeding said nitrogen enriched stream into the Claude cycle in sufficient amounts to provide makeup cycle medium.
- a process according to claim 1 further comprising precooling said one stream prior to engine expanding thereof with a refrigeration precooling cycle based on a cycle medium comprising a mixture of methane and propane ethane.
- said precooling refrigeration cycle comprising a precooling compressor and a cooler downstream of the precooling compressor, and further comprising with drawing a mixture of gas and liquid from said cooler, said liquid containing predominantly higher-boiling hydrocarbons and said gas being rich in lower-boiling components; separating the gas and the liquid; said separated gas and liquid streams in heat exchange with liquid evaporating at the suction pressure of the compressor, totally condensing said gas rich in lower-boiling components, the resultant liquid being expanded to the suction pressure of the compressor, whereby the total condensation is effected by the evaporation of the thus-formed, expanded liquid.
- said precooling refrigeration cycle comprising a precooling compressor and a cooler downstream of the precooling compressor, and further comprising with drawing a mixture of gas and liquid from said cooler, said liquid containing predominantly higher-boiling hydrocarbons and said gas being rich in lower-boiling components; separating the gas and the liquid; said separated gas and liquid streams in heat exchange with liquid evaporating at the suction pressure of the compressor, totally condensing said gas rich in lower-boiling components, the resultant liquid being expanded to the suctionpressure of the compressor, whereby the total condensation is effected by the evaporation of the thus-formed, expanded liquid.
- precooling cycle medium further comprises ethane.
- a process as defined by claim 2 wherein the maximum molar concentration in the medium is 60 percent nitrogen.
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- Mechanical Engineering (AREA)
- Thermal Sciences (AREA)
- General Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
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Applications Claiming Priority (1)
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DE19712110417 DE2110417A1 (de) | 1971-03-04 | 1971-03-04 | Verfahren zum Verfluessigen und Unterkuehlen von Erdgas |
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US00231984A Expired - Lifetime US3818714A (en) | 1971-03-04 | 1972-03-06 | Process for the liquefaction and subcooling of natural gas |
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US (1) | US3818714A (es) |
DE (1) | DE2110417A1 (es) |
FR (1) | FR2128674B1 (es) |
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US4592767A (en) * | 1985-05-29 | 1986-06-03 | Union Carbide Corporation | Process for separating methane and nitrogen |
US4617037A (en) * | 1984-11-02 | 1986-10-14 | Nippon Sanso Kabushiki Kaisha | Nitrogen production method |
US5755114A (en) * | 1997-01-06 | 1998-05-26 | Abb Randall Corporation | Use of a turboexpander cycle in liquefied natural gas process |
US5768912A (en) * | 1994-04-05 | 1998-06-23 | Dubar; Christopher Alfred | Liquefaction process |
US6016665A (en) * | 1997-06-20 | 2000-01-25 | Exxon Production Research Company | Cascade refrigeration process for liquefaction of natural gas |
US6070429A (en) * | 1999-03-30 | 2000-06-06 | Phillips Petroleum Company | Nitrogen rejection system for liquified natural gas |
US6085547A (en) * | 1998-09-18 | 2000-07-11 | Johnston; Richard P. | Simple method and apparatus for the partial conversion of natural gas to liquid natural gas |
US6085545A (en) * | 1998-09-18 | 2000-07-11 | Johnston; Richard P. | Liquid natural gas system with an integrated engine, compressor and expander assembly |
US6085546A (en) * | 1998-09-18 | 2000-07-11 | Johnston; Richard P. | Method and apparatus for the partial conversion of natural gas to liquid natural gas |
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US4017283A (en) * | 1971-11-17 | 1977-04-12 | Sulzer Brothers Limited | Method and plant for making up nitrogen vaporization losses in nitrogen-containing liquified natural gas carrying tankers |
US3970441A (en) * | 1973-07-17 | 1976-07-20 | Linde Aktiengesellschaft | Cascaded refrigeration cycles for liquefying low-boiling gaseous mixtures |
US4072485A (en) * | 1976-01-30 | 1978-02-07 | Compagnie Francaise D'etudes Et De Construction - Technip | Method of and arrangement for processing through low temperature heat exchanges and in particular for treating natural gases and cracked gases |
US4461634A (en) * | 1980-10-16 | 1984-07-24 | Petrocarbon Developments Limited | Separation of gas mixtures by partial condensation |
US4501600A (en) * | 1983-07-15 | 1985-02-26 | Union Carbide Corporation | Process to separate nitrogen from natural gas |
US4617037A (en) * | 1984-11-02 | 1986-10-14 | Nippon Sanso Kabushiki Kaisha | Nitrogen production method |
US4592767A (en) * | 1985-05-29 | 1986-06-03 | Union Carbide Corporation | Process for separating methane and nitrogen |
US5768912A (en) * | 1994-04-05 | 1998-06-23 | Dubar; Christopher Alfred | Liquefaction process |
US5755114A (en) * | 1997-01-06 | 1998-05-26 | Abb Randall Corporation | Use of a turboexpander cycle in liquefied natural gas process |
US6016665A (en) * | 1997-06-20 | 2000-01-25 | Exxon Production Research Company | Cascade refrigeration process for liquefaction of natural gas |
US6085547A (en) * | 1998-09-18 | 2000-07-11 | Johnston; Richard P. | Simple method and apparatus for the partial conversion of natural gas to liquid natural gas |
US6085545A (en) * | 1998-09-18 | 2000-07-11 | Johnston; Richard P. | Liquid natural gas system with an integrated engine, compressor and expander assembly |
US6085546A (en) * | 1998-09-18 | 2000-07-11 | Johnston; Richard P. | Method and apparatus for the partial conversion of natural gas to liquid natural gas |
US6269656B1 (en) | 1998-09-18 | 2001-08-07 | Richard P. Johnston | Method and apparatus for producing liquified natural gas |
US6070429A (en) * | 1999-03-30 | 2000-06-06 | Phillips Petroleum Company | Nitrogen rejection system for liquified natural gas |
US20040255616A1 (en) * | 2001-08-21 | 2004-12-23 | Maunder Anthony D. | Method for liquefying methane-rich gas |
GB2393504B (en) * | 2001-08-21 | 2005-05-18 | Gasconsult Ltd | Method for liquefying methane-rich gas |
WO2003019095A1 (en) * | 2001-08-21 | 2003-03-06 | Gasconsult Limited | Method for liquefying methane-rich gas |
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Also Published As
Publication number | Publication date |
---|---|
DE2110417A1 (de) | 1972-09-21 |
FR2128674A1 (es) | 1972-10-20 |
FR2128674B1 (es) | 1976-07-09 |
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