US3721099A - Fractional condensation of natural gas - Google Patents
Fractional condensation of natural gas Download PDFInfo
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- US3721099A US3721099A US00022233A US3721099DA US3721099A US 3721099 A US3721099 A US 3721099A US 00022233 A US00022233 A US 00022233A US 3721099D A US3721099D A US 3721099DA US 3721099 A US3721099 A US 3721099A
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- Prior art keywords
- liquid
- nitrogen
- column
- natural gas
- gas
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- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 title abstract description 132
- 239000003345 natural gas Substances 0.000 title abstract description 37
- 238000009833 condensation Methods 0.000 title abstract description 19
- 230000005494 condensation Effects 0.000 title abstract description 19
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract description 115
- 239000007788 liquid Substances 0.000 abstract description 92
- 229910052757 nitrogen Inorganic materials 0.000 abstract description 58
- 239000007789 gas Substances 0.000 abstract description 38
- 238000000034 method Methods 0.000 abstract description 18
- 238000010992 reflux Methods 0.000 abstract description 6
- 239000000203 mixture Substances 0.000 description 19
- 238000005057 refrigeration Methods 0.000 description 17
- 238000009835 boiling Methods 0.000 description 11
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 9
- 229930195733 hydrocarbon Natural products 0.000 description 9
- 150000002430 hydrocarbons Chemical class 0.000 description 9
- 239000012071 phase Substances 0.000 description 9
- 238000004891 communication Methods 0.000 description 8
- 238000001704 evaporation Methods 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 8
- 239000007792 gaseous phase Substances 0.000 description 7
- 241000196324 Embryophyta Species 0.000 description 6
- 239000008246 gaseous mixture Substances 0.000 description 6
- PMMNWNQXYGZXKY-UHFFFAOYSA-N CC.C.[N] Chemical compound CC.C.[N] PMMNWNQXYGZXKY-UHFFFAOYSA-N 0.000 description 5
- 238000001816 cooling Methods 0.000 description 4
- 230000008020 evaporation Effects 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 238000010792 warming Methods 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- 241000218652 Larix Species 0.000 description 1
- 235000005590 Larix decidua Nutrition 0.000 description 1
- 241001446467 Mama Species 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 239000003949 liquefied natural gas Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- 150000002829 nitrogen Chemical class 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 238000005201 scrubbing Methods 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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- 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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- F25J1/0022—Hydrocarbons, e.g. natural gas
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- F25J2200/06—Processes or apparatus using separation by rectification in a dual pressure main column system in a classical double column flow-sheet, i.e. with thermal coupling by a main reboiler-condenser in the bottom of low pressure respectively top of high pressure column
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
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- Y10S62/00—Refrigeration
- Y10S62/927—Natural gas from nitrogen
Definitions
- This invention relates to a system for the liquefaction of natural gas by fractional condensation under pressure, wherein the nitrogen in the natural gas is separated by rectification.
- Still another object is to provide an improved system wherein nitrogen is removed from the natural gas in such a manner that minimal refrigeration energy is required.
- Any portion of said mixture not fed into the high pressure column is expanded, evaporated and warmed in heat exchange with fractions to be snbcooled and fed to the low pressure rectification stage. Said portion is then employed in the precooling system, and subsequently compressed and recycled into the natural gas to be liquefied.
- the sump liquid from the high-pressure column is likewise snbcooled and expanded into the upper column. From the sump of the upper column, there is withdrawn liquid methane low in nitrogen and containing ethane, and this product is then snbcooled prior to being fed into the storage tank.
- the subcooling is conducted by heat exchange with expanded nitrogen withdrawn in the gaseous phase from the high-pressure column or from both the high-pressure column and the low-pressure column, said nitrogen being additionally warmed against fractions to be snbcooled and fed to the rectification column.
- An important advantage of this invention is that the pressure of the natural gas is utilized in an especially energy-conserving manner, on the one hand for the production of peak refrigeration levels and, on the other hand, for the separation of nitrogen.
- the latter is withdrawn from the rectification column either as a substantially pure nitrogen fraction and used for various known purposes as such, or it is employed as a component of town gas in the form of an impure nitrogen fraction to which have been added higher hydrocarbons for adjusting the heating value.
- liquid methane containing nitrogen and ethane is separated, by partial condensation in the precooling system, from the nitrogen-methane-ethane gaseous mixture remaining in the gaseous phase after the fractional condensation of the hydrocarbons required for the production of refrigeration in the precooling system, and prior to the heat exchange of said gaseous mixture with the sump liquid of the highpressure column.
- This liquid methane optionally in admixture with the sump liquid of the high-pressure column, and after a subcooling step, is preferably expanded into the upper low-pressure column, but can also be expanded, evaporated and warmed in heat exchange with fractions to be snbcooled and fed to the low-pressure rectification stage. In this manner preliminary nitrogen enrichment is achieved inn the gaseous phase.
- Another preferred embodiment of the process according to the invention resides in providing that the liquid formed by heat exchange with the sump liquid of the high-pressure column is expanded into the high-pressure column, and that liquid is withdrawn from this column at another point, expanded, evaporated and warmed in heat exchange with fractions being fed to the rectification column; thereafter passed through the precooling system; and then compressed and recycled into the natural gas to be liquefied.
- the advantage of this technique is that the point of liquid withdrawal from the column, i.e. the composition of the liquid and thus the boiling point thereof, can be adjusted so that exactly the desired temperature is ambient at the cold end of the heat exchanger wherein this liquid is evaporated.
- the precooling system It is especially suitable first to subcool the sump liquid of the high-pressure column and/or the liquid formed in heat exchange therewith, after leaving the high-pressure column, in the precooling system. Also the liquid which has been formed (after separating the liquid required in the precooling stage for cold production) by additional partial condensation of the remaining gaseous mixture in the precooling system is advantageously first subcooled in the precooling system. This procedure serves to increase the amount of liquid to be introduced into the column.
- the residual portion of the liquid formed by heat exchange with the sump liquid of the high-pressure column, or the liquid withdrawn from the high-pressure column at another point, is subcooled prior to expansion thereof, by countercurrent heat exchange with itself and/or with fractionation products, in order to reduce the amount of vapor formed during the subsequent expansion.
- the apparatus for conducting the process of this invention is characterized in that a middle section of the high-pressure column of a double rectification column is in communication with a precooling system for the partial condensation of natural gas via a feed conduit, provided with an expansion valve, for liquid methane containing nitrogen and ethane.
- the sump of the high-pressure column is in communication with the upper column of the double rectification column via a liquid conduit provided with an expanson valve.
- a conduit for gaseous nitrogen is connected from the head of the high-pressure column, by way of an expansion valve, with the refrigerating medium side of a heat exchanger, the flow path of said heat exchanger for material to be cooled being in communication, on the one hand, with the sump of the upper column and, on the other hand, with a storage tank for liquid methane.
- Thep recooling system is connected downstream of the refrigerating medium side of said heat exchanger via at least one additional heat exchanger for subcooling liquids being fed to the rectification stage.
- FIG. 1 shows the details of the precooling system whereas the other figures depict same in block form.
- An example of a natural gas to be processed exhibits the following composition:
- the CO Prior to entering the low-temperature plant, the CO is removed by a monoethanolamine scrubbing step, and the gaseous water is removed by exchangeable molecular sieve 4 adsorbers.
- the natural gas then enters the low-temperature plant through conduit 1 at a pressure of about 30 to 45, preferably 35 atmospheres, but can also be fed into one of the previous cycle gas compressor stages, and is mixed with cycle gas at 2, and cooled in heat exchanger 3. Thereby, a condensate is produced containing predominantly higher-boiling hydrocarbons, which condensate is separated from the gas in the phase separator 4. Both the gas and the liquid are further cooled in heat exchanger 5.
- the liquid is then expanded in valve 6 into the returning cycle gas, the latter having been formed by the evaporation of lower-boiling liquids in heat exchangers operating at a lower temperature. It is then evaporated and warmed in heat exchangers and 3, and finally fed, via the phase separator 7, to the first compressor stage 8 and the intercooling stage 9 connected thereafter.
- the thus-formed liquid collects in the phase separator 10.
- Another compressor stage 11 follows, with cooler 12 and separator 13.
- the portion remaining in the gaseous phase is fed at 2 into the natural gas to be liquefied.
- the liquid separately withdrawn from the separators and 13 is subcooled in heat exchanger 3 and expanded (pressure reduced) into the cycle gas through valves 14 and 15, respectively.
- the gas leaving the separator 4 and partially condensed in heat exchanger 5 is separated, in the separator 16, from the thus-formed liquid and again subjected to a partial condensation in the heat exchanger 17, passing via the separator 18 and the additional heat exchanger 19 into the separator 20.
- the amount of liquid produced up to this point is sufficient to compensate for the refrigerating requirements of the precooling system.
- This liquid is then subcooled, namely, the liquid from separator 16 in the heat exchanger 17, the liquid from separator 18 in heat exchangers 19, 21 and 22, and the liquid from separator in heat exchangers 21, 22 and 23. Thereafter, the liquid is expanded into the cycle gas by means of the valves 24 and 25 and 26, respectively.
- the thus-formed fiuid mixture is then recycled, as cycle gas, into the natural gas to be liquefied, as set out above.
- the gas discharged from the separator 20 contains the entire amount of methane to be liquefied, a corresponding proportion of nitrogen, as well as minor amounts of ethane.
- This gas is cooled in heat exchanger 21 to such an extent that the gaseous phase in the separator 27 contains approximately 25% nitrogen and the liquid phase, in correspondence with the equilibrium, contains about 5% nitrogen.
- the resultant gas is liquefied and subcooled in the pipe coil 28 which heats the sump of the high-pressure column 29 of the double rectification column, and is passed thereafter through the heat exchanger 23 involved in the precooling system.
- a portion of the liquid from heat exchanger 23 is expanded, via valve 30, into the high-pressure column 29 operating at 22 atmospheres absolute; in this high-pressure column, the head product obtained is a substantially pure nitrogen fraction containing only about 5% methane, and the sump product is a liquid, the composition of which is approximately the same as that of the liquid obtained in the separator 27, i.e. 5% nitrogen.
- the resultant evaporated liquid finally passes, together with the liquid expanded in valve 26 (the evaporation temperature of the latter liquid representing the lowest of the precooling system) through the cycle back to the compressor.
- the liquid from the separator 27 is subcooled in heat exchanger 22 and then, like the sump liquid of the highpressure column, further subcooled in heat exchangers 23 and 31, and introduced through valves 33 and 34, respectively, into the upper column 35 of the double rectifier, operating at about 2.5 atmospheres absolute.
- To this upper column is fed, via expansion valve 36, liquid reflux nitrogen previously subcooled in the heat exchangers 31 and 37, and derived from the top part of the high-pressure column.
- As the overhead product of the upper column there is obtained a gas having 95 molar percent of nitrogen, and to this gas is added, via valve 38, heliumenriched nitrogen from the head of the high-pressure column.
- liquid methane containing about 015% nitrogen and approximately 2% ethane.
- This liquid methane is subcooled in heat exchanger 37 by gaseous nitrogen and expanded into the tank 39, the latter being operated at a superatmospheric pressure of about 350 mm. H O.
- Continuously evaporating gas formed due to the imperfect insulation of the tank 39 is withdrawn via conduit 40, compressed in the cold gas blower 41 and warmed in heat exchanger 31 and in the precooling system.
- the higher-boiling hydrocarbons to be separated in the precooling section are admixed to this gas via valves 42 and 43.
- the system according to FIG. 2 differs from the abovedescribed system in that there is discharged from the plant, in addition to liquid methane and a pure nitrogen fraction, a gaseous mixture having approximately the heating value of the natural gas.
- the gas coming from the phase separator 27 is liquefied and subcooled in the coil 28 and in the precooling system, and is then further subcooled in countercurrent heat exchanger 44. Thereafter it is expanded, in part, through valve 30 into the high-pressure column 29 and, in part, after being subcooled in the countercurrent heat exchanger 31, through valve 32.
- the thus liberated refrigeration is transferred, in heat exchangers 31 and 44, to the liquid fractions passing to the rectification stage.
- the resultant fluid is warmed in the precooling system and then recycled into the natural gas to be liquefied.
- the liquid from the separator 27 is expanded in valve 45 to the pressure of the high pressure column and, together with the sump liquid of the high-pressure column, subcooled first in the precooling system and thereafter in the heat exchangers 44 and 31, and then expanded via valve 34a into the upper column 35.
- the gaseous stream withdrawn from the head of this upper column contains, in addition to nitrogen, about 80% methane; this gaseous stream is mixed with the gas evaporating in the storage tank, the latter gas having been compressed by the cold gas blower 41 to about 1.8 atm. abs., and warmed, via conduit 40a, in heat exchangers 31 and 44, as well as in the precooling system.
- valve 42a higher-boiling hydrocarbons pre viously condensed during the course of the precooling step.
- a gaseous substantially pure nitrogen fraction at a pressure of 22 atm. abs. is withdrawn as the overhead product, expanded in valve 38, and first warmed in the heat exchanger 37a against methane so that the latter is subcooled.
- the residual refrigeration capacity of the nitrogen stream is transferred, in heat exchangers 31 and 44, to the fractions passing to the rectification column and then further utilized in the precooling system.
- FIG. 3 depicts an embodiment of the invention wherein the liquid formed in the pipe coil 28, after being subcooled in the precooling system and in the heat exchanger 44a, is fed in its entirety into the high-pressure column via valve 30.
- the substantially pure gaseous nitrogen fraction withdrawn from the highpressure column 29 'via expansion in valve 38. This nitrogen stream, after being warmed in heat exchangers 37a and 44a and then in the precooling system, is discharged from the plant.
- FIG. 4 depicts an embodiment of the invention wherein, as in the process shown in FIG. 1, no gas need be discharged as town gas, so that the undesired nitrogen can be separated in as enriched a form as possible as a purer nitrogen fraction.
- the natural gas to be liquefied after the hydrocarbons necessary for refrigeration production in the precooling system have been liquefied and separated, is liquefied without prior partial condensation in the pipe coil 28 and then subcooled in the precooling system, and in the heat exchanger 441). It is then completely expanded via valve 30 into the high-pressure column 29.
- the sump liquid of the high-pressure column is passed via expansion valve 341; into the upper column.
- liquid is withdrawn from the high-pressure column via conduit 47, subcooled in heat exchanger 31b, and expanded in 'valve 32a.
- this refrigeration is transferred to the fractions fed to the low-pressure column.
- the thus-produced gas is further warmed in the precooling system, then compressed, and finally recycled into the natural gas to be liquefied.
- the advantage of this embodiment resides in that the composition of the liquid to be expanded in valve 32a, and thus the temperature at the cold end of the heat exchanger 31b, can be adapted to existing conditions in an especially advantageous manner by an appropriate selection of the point of withdrawal. Since, just as in the process according to FIG.
- the improvement comprising liquefying a gaseous nitrogen-methane-ethane mixture remaining after the fractional condensation of the hydrocarbon fraction required for the production of refrigeration in the precooling system, said liquefying being conducted by passing said mixture in heat exchange with sump liquid of a high-pressure column of a double rectification column; expanding resultant liquid at least partially, into the high-pressure column; separating said expanded liquid in said high-pressure column into a substantially pure gaseous nitrogen fraction, as the head product of the high-pressure column, and into a methane fraction containing nitrogen and ethane, as the sump liquid; withdrawing and expanding said substantially pure gaseous nitrogen fraction; subcooling and expanding the sump liquid from the high-pressure column and passing same into the lowpressure column; withdrawing from the sump of the low-pressure column liquid methane low in nitrogen and containing ethane, and subcooling said liquid methane by passing same in indirect heat exchange with said substantially pure expanded nitrogen fraction, whereby peak cooling is attained.
- Apparatus for liquefying natural gas and removing nitrogen therefrom comprising precooling means for the partial condensation of natural gas comprising an open cycle containing a plurality of serially connected heat exchangers, a plurality of serially connected phase separators, expansion means, compressor means, and natural gas feed means, a high-pressure column (29) of a double rectification column, said highpressure column (29) being in communication with the gas side of the most downstream phase separator, a conduit for said communication provided with cooling means (21); phase separator means (27); coil means (28) in the sump of the high-pressure column and an expansion valve (30), the sump of the high-pressure column (29) being in communication with an upper column (35) of the double rectification column via a liquid conduit provided with an expansion valve (34; 34a; 34b); a heat exchanger (37; 37a); a conduit for gaseous nitrogen being connected from the head of the high-pressure column (29), by way of an expansion valve (38), with the refrigerating medium side of said
- Apparatus as defined by claim 8 further comprising conduit means for effect communication between the liquid side of said phase separator (27) and the top of the upper column (35), said conduit means being provided with an expansion valve (34a); and further heat exchange means (44a) for cooling feed streams to the double rectification column against nitrogen fractions withdrawn from said column.
- gaseous nitrogen-methane-ethane mixture is derived from a gaseous stream withdrawn from a single phase separator in said precooling cycle, said stream containing the entire amount of methane to be liquefied, said gaseous stream being subjected to further cooling and further phase separation to obtain said gaseous nitrogen-methane-ethane mixture.
Abstract
A SYSTEM FOR THE LIQUEFACTION OF NATURAL GAS WHEREIN NITROGEN IS REMOVED FROM THE GAS BY RECTIFICATION, INVOLVES FRACTIONAL CONDENSATION OF THE NATURAL GAS AND PASSING A GASEOUS PORTION OF THE THUS-TREATED GAS THROUGH THE SUMP OF A RECTIFICATION COLUMN, IN INDIRECT HEAT EXCHANGE WITH SUMP LIQUID. AT LEAST A PORTION OF THE RESULTANT CONDENSED GASEOUS PORTION IS RETURNED TO THE RECTIFICATION COLUMN AS FEED THROUGH AN EXPANSION VALUE. HEAT EXCHANGERS ARE EMPLOYED TO SUBCOOL NATURAL GAS LIQUID PASSING TO THE STORAGE TANK AND REFLUX LIQUID PASSING TO THE RECTIFICATION COLUMN, SAID HEAT EXCHANGERS BEING COOLED BY NITROGEN FRACTIONS WITHDRAW FROM THE RECTIFICATION COLUMN. THE OVERALL SYSTEM PROVIDES FOR SAVINGS IN RECTIFICATION ENERGY, AND ALSO PROVIDES PEAK REFRIGATION LOADS FOR START-UP PROCEDURES AND THE LIKE.
Description
March 20, 1973 w. FORG. ET A1. 3, fl9
FRACTIONAL CONDENSATION OF NATURAL GAS Filed March 24, 1970 4 Sheets-Sheet 1 fig. 7
INVENTQRS WOLFGANG FORG VOLKER ETZBACH ATTORNEYS mamas Malfch 20, 1973 w o ET AL I FRACTIONAL CONDENSATION OF NATURAL GAS 4 Sheets-Sheet 2 Filed larch 24, 1970 1 w I llllw l1 1 m Q "mm H 7 w 2 w w w A /,T m AT%/0 3 3 q F n w w L m 2 a h n H i h a o a Q 4 3 H INVENIORS WOLFGANG FORG ATTORNEYS w. FORG ET AL 43,721,099
FRACTIONAL CONDENSATION OF NATURAL GAS Filgd March 24, 1970 March 20, 1973' 4 Sheets-Sheet 4 ll llllllllllllllllllv PRECOOLING SYSTEM Fig.4
United States Patent O US. Cl. 6229 Claims ABSTRACT OF THE DISCLOSURE A system for the liquefaction of natural gas wherein nitrogen is removed from the gas by rectification, involves fractional condensation of the natural gas and passing a gaseous portion of the thus-treated gas through the sump of a rectification column, in indirect heat exchange with sump liquid. At least a portion of the resultant condensed gaseous portion is returned to the rectification column as feed through an expansion valve. Heat exchangers are employed to subcool natural gas liquid passing to the storage tank and reflux liquid passing to the rectification column, said heat exchangers being cooled by nitrogen fractions withdrawn from the rectification column. The overall system provides for savings in refrigeration energy, and also provides peak refrigeration loads for start-up procedures and the like.
BACKGROUND OF THE INVENTION This invention relates to a system for the liquefaction of natural gas by fractional condensation under pressure, wherein the nitrogen in the natural gas is separated by rectification.
During natural gas liquefaction, it is advantageous to separate the nitrogen, otherwise it would significantly depress the boiling point and storage temperature of the resultant liquid natural gas. In other words, the presence of nitrogen in the liquefied gas would make it necessary to generate refrigeration at a temperature level below that of boiling temperature of methane. Furthermore, since the nitrogen-containing methane continuously evaporating because of imperfect insulation in the storage tank initially exhibits a high nitrogen concentration, but then decreases with increasing storage time, neither the composition of the liquid gas nor that of the evaporating gas remains constant. This means that for end uses, the composition of the supplied gas must be constantly monitored and must be adjusted to the desired, constant composition by admixing in each case the necessary quantity of one or more other gases.
SUMMARY OF THE INVENTION It is thus an object of this invention to provide an improved process and apparatus for the removal of a low boiling component during the liquefaction of a higher boiling component, and especially wherein nitrogen is the low boiling component and natural gas is the high boiling component.
Still another object is to provide an improved system wherein nitrogen is removed from the natural gas in such a manner that minimal refrigeration energy is required.
Upon further study of the specification and appended claims, other objects and advantages of the present invention will become apparent.
These objects are attained, with reference to nitrogen removal from natural gas, by providing a nitrogenmethane-ethane mixture which remains in the gaseous phase after the fractional condensation of the hydrocarice bons required for the production of refrigeration in the precooling system. This mixture is liquefied by heat exchange against the sump liquid of a high-pressure column of a double rectification column (or equivalent thereof) and is expanded, at least partially, into the high-pressure column, to be separated therein into a substantially pure nitrogen fraction, as the overhead product, and into a methane fraction containing nitrogen and ethane, as the sump liquid.
Any portion of said mixture not fed into the high pressure column is expanded, evaporated and warmed in heat exchange with fractions to be snbcooled and fed to the low pressure rectification stage. Said portion is then employed in the precooling system, and subsequently compressed and recycled into the natural gas to be liquefied.
The sump liquid from the high-pressure column is likewise snbcooled and expanded into the upper column. From the sump of the upper column, there is withdrawn liquid methane low in nitrogen and containing ethane, and this product is then snbcooled prior to being fed into the storage tank. The subcooling is conducted by heat exchange with expanded nitrogen withdrawn in the gaseous phase from the high-pressure column or from both the high-pressure column and the low-pressure column, said nitrogen being additionally warmed against fractions to be snbcooled and fed to the rectification column.
An important advantage of this invention is that the pressure of the natural gas is utilized in an especially energy-conserving manner, on the one hand for the production of peak refrigeration levels and, on the other hand, for the separation of nitrogen. The latter is withdrawn from the rectification column either as a substantially pure nitrogen fraction and used for various known purposes as such, or it is employed as a component of town gas in the form of an impure nitrogen fraction to which have been added higher hydrocarbons for adjusting the heating value.
DETAILED DISCUSSION OF THE INVENTION In a further embodiment of the invention, liquid methane containing nitrogen and ethane is separated, by partial condensation in the precooling system, from the nitrogen-methane-ethane gaseous mixture remaining in the gaseous phase after the fractional condensation of the hydrocarbons required for the production of refrigeration in the precooling system, and prior to the heat exchange of said gaseous mixture with the sump liquid of the highpressure column. This liquid methane, optionally in admixture with the sump liquid of the high-pressure column, and after a subcooling step, is preferably expanded into the upper low-pressure column, but can also be expanded, evaporated and warmed in heat exchange with fractions to be snbcooled and fed to the low-pressure rectification stage. In this manner preliminary nitrogen enrichment is achieved inn the gaseous phase.
Another preferred embodiment of the process according to the invention resides in providing that the liquid formed by heat exchange with the sump liquid of the high-pressure column is expanded into the high-pressure column, and that liquid is withdrawn from this column at another point, expanded, evaporated and warmed in heat exchange with fractions being fed to the rectification column; thereafter passed through the precooling system; and then compressed and recycled into the natural gas to be liquefied. The advantage of this technique is that the point of liquid withdrawal from the column, i.e. the composition of the liquid and thus the boiling point thereof, can be adjusted so that exactly the desired temperature is ambient at the cold end of the heat exchanger wherein this liquid is evaporated.
It is especially suitable first to subcool the sump liquid of the high-pressure column and/or the liquid formed in heat exchange therewith, after leaving the high-pressure column, in the precooling system. Also the liquid which has been formed (after separating the liquid required in the precooling stage for cold production) by additional partial condensation of the remaining gaseous mixture in the precooling system is advantageously first subcooled in the precooling system. This procedure serves to increase the amount of liquid to be introduced into the column.
In a still further preferred embodiment, the residual portion of the liquid formed by heat exchange with the sump liquid of the high-pressure column, or the liquid withdrawn from the high-pressure column at another point, is subcooled prior to expansion thereof, by countercurrent heat exchange with itself and/or with fractionation products, in order to reduce the amount of vapor formed during the subsequent expansion.
Any residual portion of the liquid formed by heat exchange with the sump liquid of the high-pressure column, or the liquid withdrawn from the high-pressure column at another point, after expansion and partial warming, is further warmed, preferably in a mixture with the recycled cycle gas of the precooling system, and then compressed and recycled into the natural gas to be liquefied.
The apparatus for conducting the process of this invention is characterized in that a middle section of the high-pressure column of a double rectification column is in communication with a precooling system for the partial condensation of natural gas via a feed conduit, provided with an expansion valve, for liquid methane containing nitrogen and ethane. The sump of the high-pressure column is in communication with the upper column of the double rectification column via a liquid conduit provided with an expanson valve. A conduit for gaseous nitrogen is connected from the head of the high-pressure column, by way of an expansion valve, with the refrigerating medium side of a heat exchanger, the flow path of said heat exchanger for material to be cooled being in communication, on the one hand, with the sump of the upper column and, on the other hand, with a storage tank for liquid methane. Thep recooling system is connected downstream of the refrigerating medium side of said heat exchanger via at least one additional heat exchanger for subcooling liquids being fed to the rectification stage.
BRIEF DESCRIPTION OF THE DRAWINGS All the figures are schematic flowsheets depicting various preferred embodiments of the invention.
FIG. 1 shows the details of the precooling system whereas the other figures depict same in block form.
DETAILED DESCRIPTION OF THE DRAWINGS The invention will now be explained by way of example with reference to the drawings. Identical components are characterized in all figures by the same numerals.
An example of a natural gas to be processed exhibits the following composition:
Mol percent In general, however, natural gas contains a predominant amount of methane and about 2 to 40% by volume of nitrogen.
Prior to entering the low-temperature plant, the CO is removed by a monoethanolamine scrubbing step, and the gaseous water is removed by exchangeable molecular sieve 4 adsorbers. The natural gas then enters the low-temperature plant through conduit 1 at a pressure of about 30 to 45, preferably 35 atmospheres, but can also be fed into one of the previous cycle gas compressor stages, and is mixed with cycle gas at 2, and cooled in heat exchanger 3. Thereby, a condensate is produced containing predominantly higher-boiling hydrocarbons, which condensate is separated from the gas in the phase separator 4. Both the gas and the liquid are further cooled in heat exchanger 5.
The liquid is then expanded in valve 6 into the returning cycle gas, the latter having been formed by the evaporation of lower-boiling liquids in heat exchangers operating at a lower temperature. It is then evaporated and warmed in heat exchangers and 3, and finally fed, via the phase separator 7, to the first compressor stage 8 and the intercooling stage 9 connected thereafter. The thus-formed liquid collects in the phase separator 10. Another compressor stage 11 follows, with cooler 12 and separator 13. The portion remaining in the gaseous phase is fed at 2 into the natural gas to be liquefied. The liquid separately withdrawn from the separators and 13 is subcooled in heat exchanger 3 and expanded (pressure reduced) into the cycle gas through valves 14 and 15, respectively.
The gas leaving the separator 4 and partially condensed in heat exchanger 5 is separated, in the separator 16, from the thus-formed liquid and again subjected to a partial condensation in the heat exchanger 17, passing via the separator 18 and the additional heat exchanger 19 into the separator 20. The amount of liquid produced up to this point is sufficient to compensate for the refrigerating requirements of the precooling system. This liquid is then subcooled, namely, the liquid from separator 16 in the heat exchanger 17, the liquid from separator 18 in heat exchangers 19, 21 and 22, and the liquid from separator in heat exchangers 21, 22 and 23. Thereafter, the liquid is expanded into the cycle gas by means of the valves 24 and 25 and 26, respectively. The thus-formed fiuid mixture is then recycled, as cycle gas, into the natural gas to be liquefied, as set out above.
The gas discharged from the separator 20 contains the entire amount of methane to be liquefied, a corresponding proportion of nitrogen, as well as minor amounts of ethane. This gas is cooled in heat exchanger 21 to such an extent that the gaseous phase in the separator 27 contains approximately 25% nitrogen and the liquid phase, in correspondence with the equilibrium, contains about 5% nitrogen. The resultant gas is liquefied and subcooled in the pipe coil 28 which heats the sump of the high-pressure column 29 of the double rectification column, and is passed thereafter through the heat exchanger 23 involved in the precooling system.
A portion of the liquid from heat exchanger 23 is expanded, via valve 30, into the high-pressure column 29 operating at 22 atmospheres absolute; in this high-pressure column, the head product obtained is a substantially pure nitrogen fraction containing only about 5% methane, and the sump product is a liquid, the composition of which is approximately the same as that of the liquid obtained in the separator 27, i.e. 5% nitrogen.
The remaining liquid from the pipe coil 28, instead of being passed through valve 39, is subcooled in heat exchanger 31, expanded in valve 32, and evaporated in heat exchanger 31, thereby transferring its latent cold of evaporation during this step, to the fractions passing to the upper column. The resultant evaporated liquid finally passes, together with the liquid expanded in valve 26 (the evaporation temperature of the latter liquid representing the lowest of the precooling system) through the cycle back to the compressor.
The liquid from the separator 27 is subcooled in heat exchanger 22 and then, like the sump liquid of the highpressure column, further subcooled in heat exchangers 23 and 31, and introduced through valves 33 and 34, respectively, into the upper column 35 of the double rectifier, operating at about 2.5 atmospheres absolute. To this upper column is fed, via expansion valve 36, liquid reflux nitrogen previously subcooled in the heat exchangers 31 and 37, and derived from the top part of the high-pressure column. As the overhead product of the upper column there is obtained a gas having 95 molar percent of nitrogen, and to this gas is added, via valve 38, heliumenriched nitrogen from the head of the high-pressure column. This resultant gaseous mixture is warmed in the heat exchangers 37 and 31, as well as in the precooling system, and is then withdrawn from the plant. Owing to the low methane concentration in the nitrogen, the losses in methane are kept at a minimum.
In the sump of the low-pressure column 35 there is collected liquid methane containing about 015% nitrogen and approximately 2% ethane. This liquid methane is subcooled in heat exchanger 37 by gaseous nitrogen and expanded into the tank 39, the latter being operated at a superatmospheric pressure of about 350 mm. H O. Continuously evaporating gas formed due to the imperfect insulation of the tank 39 is withdrawn via conduit 40, compressed in the cold gas blower 41 and warmed in heat exchanger 31 and in the precooling system. During this procedure, the higher-boiling hydrocarbons to be separated in the precooling section are admixed to this gas via valves 42 and 43.
The system according to FIG. 2 differs from the abovedescribed system in that there is discharged from the plant, in addition to liquid methane and a pure nitrogen fraction, a gaseous mixture having approximately the heating value of the natural gas. The gas coming from the phase separator 27 is liquefied and subcooled in the coil 28 and in the precooling system, and is then further subcooled in countercurrent heat exchanger 44. Thereafter it is expanded, in part, through valve 30 into the high-pressure column 29 and, in part, after being subcooled in the countercurrent heat exchanger 31, through valve 32. The thus liberated refrigeration is transferred, in heat exchangers 31 and 44, to the liquid fractions passing to the rectification stage. Finally, the resultant fluid is warmed in the precooling system and then recycled into the natural gas to be liquefied.
The liquid from the separator 27 is expanded in valve 45 to the pressure of the high pressure column and, together with the sump liquid of the high-pressure column, subcooled first in the precooling system and thereafter in the heat exchangers 44 and 31, and then expanded via valve 34a into the upper column 35. The gaseous stream withdrawn from the head of this upper column contains, in addition to nitrogen, about 80% methane; this gaseous stream is mixed with the gas evaporating in the storage tank, the latter gas having been compressed by the cold gas blower 41 to about 1.8 atm. abs., and warmed, via conduit 40a, in heat exchangers 31 and 44, as well as in the precooling system. In order to adjust the heating value of this gaseous mixture to that of natural gas, there are added via valve 42a higher-boiling hydrocarbons pre viously condensed during the course of the precooling step.
From the high-pressure column 29 a gaseous substantially pure nitrogen fraction at a pressure of 22 atm. abs. is withdrawn as the overhead product, expanded in valve 38, and first warmed in the heat exchanger 37a against methane so that the latter is subcooled. The residual refrigeration capacity of the nitrogen stream is transferred, in heat exchangers 31 and 44, to the fractions passing to the rectification column and then further utilized in the precooling system.
Optionally, it is also possible to branch off reflux liquid and expand same through valve 46 into conduit 40a in order to have additional peak refrigeration available, for example, when placing the plant on stream, for the operation of the heat exchanger 31.
FIG. 3 depicts an embodiment of the invention wherein the liquid formed in the pipe coil 28, after being subcooled in the precooling system and in the heat exchanger 44a, is fed in its entirety into the high-pressure column via valve 30. For subcooling the liquid methane in heat exchanger 37a, there is again employed the substantially pure gaseous nitrogen fraction withdrawn from the highpressure column 29 'via expansion in valve 38. This nitrogen stream, after being warmed in heat exchangers 37a and 44a and then in the precooling system, is discharged from the plant.
FIG. 4 depicts an embodiment of the invention wherein, as in the process shown in FIG. 1, no gas need be discharged as town gas, so that the undesired nitrogen can be separated in as enriched a form as possible as a purer nitrogen fraction. In this connection, the natural gas to be liquefied, after the hydrocarbons necessary for refrigeration production in the precooling system have been liquefied and separated, is liquefied without prior partial condensation in the pipe coil 28 and then subcooled in the precooling system, and in the heat exchanger 441). It is then completely expanded via valve 30 into the high-pressure column 29. The sump liquid of the high-pressure column is passed via expansion valve 341; into the upper column. To generate peak refrigeration, liquid is withdrawn from the high-pressure column via conduit 47, subcooled in heat exchanger 31b, and expanded in 'valve 32a. In heat exchangers 31b and 4417, this refrigeration is transferred to the fractions fed to the low-pressure column. The thus-produced gas is further warmed in the precooling system, then compressed, and finally recycled into the natural gas to be liquefied. The advantage of this embodiment resides in that the composition of the liquid to be expanded in valve 32a, and thus the temperature at the cold end of the heat exchanger 31b, can be adapted to existing conditions in an especially advantageous manner by an appropriate selection of the point of withdrawal. Since, just as in the process according to FIG. 1, only the evaporation loss of the storage tank may be discharged as town gas, nitrogen in as pure a form as possible must, in turn, be obtained from the head of the low-pressure column. For this purpose, pure liquid nitrogen is withdrawn at the head of the high-pressure column, sub-cooled in heat exchangers 31b and 37, and fed via valve 36 as reflux to the upper column. From the head of this column, a gaseous pure nitrogen fraction is Withdrawn which still contains approximately 5% methane. Helium-enriched gaseous nitrogen from the head of the high-pressure column is admixed via valve 38 to the aforementioned fraction. The resultant nitrogen stream is first utilized in heat exchanger 37 for subcooling both liquid methane and reflux liquid for the upper column. It then transfers additional refrigeration, in heat exchangers 31b and 44b, to the fractions passing to the rectification column, and is finally warmed in the precooling system.
From the foregoing description, one skilled in the art can easily ascertain the essential characteristics of this invention, and without departing from the spirit and scope thereof, can make various changes and modifications of the invention to adapt it to various usages and conditions.
What is claimed is:
1. In a process for the liquefaction of natural gas by fractional condensation under pressure, and with the separation of nitrogen from said gas by rectification, wherein at least one liquid hydrocarbon fraction is, for purposes of refrigeration production, expanded in a precooling cycle, evaporated and warmed in heat exchange with media to be cooled, compressed, and recycled into the natural gas to be cooled,
the improvement comprising liquefying a gaseous nitrogen-methane-ethane mixture remaining after the fractional condensation of the hydrocarbon fraction required for the production of refrigeration in the precooling system, said liquefying being conducted by passing said mixture in heat exchange with sump liquid of a high-pressure column of a double rectification column; expanding resultant liquid at least partially, into the high-pressure column; separating said expanded liquid in said high-pressure column into a substantially pure gaseous nitrogen fraction, as the head product of the high-pressure column, and into a methane fraction containing nitrogen and ethane, as the sump liquid; withdrawing and expanding said substantially pure gaseous nitrogen fraction; subcooling and expanding the sump liquid from the high-pressure column and passing same into the lowpressure column; withdrawing from the sump of the low-pressure column liquid methane low in nitrogen and containing ethane, and subcooling said liquid methane by passing same in indirect heat exchange with said substantially pure expanded nitrogen fraction, whereby peak cooling is attained.
2. A process as defined by claim 1 wherein said resultant liquid, not expanded into the high-pressure column, is expanded, evaporated and warmed in heat exchange with streams to be subcooled and fed to the rectification column.
3. A process as defined by claim 1 wherein said liquid methane containing nitrogen and ethane is separated by partial condensation in the precooling system, from the nitrogen-methane-ethane mixture remaining in the gaseous phase after the fractional condensation of the hydrocarbons required for the production of refrigeration in the precooling system, prior to the heat exchange of said mixture with the sump liquid of the high-pressure column, said liquid methane being then expanded, after subcooling, into the upper column.
4. A process as defined by claim 1 wherein said resultant liquid mixture is expanded in its entirety into the high-pressure column.
5. A process as defined by claim 1 wherein the sump liquid from the high-pressure column is subcooled in the precooling cycle after leaving the high-pressure column.
6. A process as defined by claim 3 wherein said liquid methane is subcooled in the precooling cycle before being passed as feed to the low-pressure column.
7. A process according to claim 2 wherein said resultant liquid not expanded into the high-pressure column is warmed, after expansion and partial warming in admixture with returning cycle gas of the precooling cycle, then compressed and recycled into the natural gas to be liquefied.
8. Apparatus for liquefying natural gas and removing nitrogen therefrom, said apparatus comprising precooling means for the partial condensation of natural gas comprising an open cycle containing a plurality of serially connected heat exchangers, a plurality of serially connected phase separators, expansion means, compressor means, and natural gas feed means, a high-pressure column (29) of a double rectification column, said highpressure column (29) being in communication with the gas side of the most downstream phase separator, a conduit for said communication provided with cooling means (21); phase separator means (27); coil means (28) in the sump of the high-pressure column and an expansion valve (30), the sump of the high-pressure column (29) being in communication with an upper column (35) of the double rectification column via a liquid conduit provided with an expansion valve (34; 34a; 34b); a heat exchanger (37; 37a); a conduit for gaseous nitrogen being connected from the head of the high-pressure column (29), by way of an expansion valve (38), with the refrigerating medium side of said heat exchanger (37; 37a), the flow path of said heat exchanger for medium to be cooled being in communication with the sump of the upper column (35) and with a storage tank (39) for liquid methane.
9. Apparatus as defined by claim 8 further comprising conduit means for effect communication between the liquid side of said phase separator (27) and the top of the upper column (35), said conduit means being provided with an expansion valve (34a); and further heat exchange means (44a) for cooling feed streams to the double rectification column against nitrogen fractions withdrawn from said column.
10. A process as defined by claim 1 wherein said gaseous nitrogen-methane-ethane mixture is derived from a gaseous stream withdrawn from a single phase separator in said precooling cycle, said stream containing the entire amount of methane to be liquefied, said gaseous stream being subjected to further cooling and further phase separation to obtain said gaseous nitrogen-methane-ethane mixture.
References Cited UNITED STATES PATENTS 3,218,816 11/1965 Grenier 62-26 2,765,637 10/;1956 Etienne 6227 2,822,675 2/ 1958 Grenier 6230 1,853,743 4/1932 Pollitzer 6224 2,180,435 11/1'939 Schlitt 62-28 2,743,590 5/ 1956 Grunberg 62-28 3,327,490 6/ 1967 Grenier 62-30 3,531,943 '1 0/1970 Parnag 6'228 NORMAN YUDKOFF, Primary Examiner A. F. PURCELL, Assistant Examiner US. Cl. X.R. 6224, '40, 31
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19691915218 DE1915218B2 (en) | 1969-03-25 | 1969-03-25 | METHOD AND DEVICE FOR LIQUIFYING NATURAL GAS |
Publications (1)
Publication Number | Publication Date |
---|---|
US3721099A true US3721099A (en) | 1973-03-20 |
Family
ID=5729261
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US00022233A Expired - Lifetime US3721099A (en) | 1969-03-25 | 1970-03-24 | Fractional condensation of natural gas |
Country Status (4)
Country | Link |
---|---|
US (1) | US3721099A (en) |
DE (1) | DE1915218B2 (en) |
FR (1) | FR2035881B1 (en) |
NL (1) | NL7004170A (en) |
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US3857251A (en) * | 1971-12-27 | 1974-12-31 | Technigaz | Lng storage tank vapor recovery by nitrogen cycle refrigeration with refrigeration make-up provided by separation of same vapor |
US3914949A (en) * | 1971-02-19 | 1975-10-28 | Chicago Bridge & Iron Co | Method and apparatus for liquefying gases |
US3970441A (en) * | 1973-07-17 | 1976-07-20 | Linde Aktiengesellschaft | Cascaded refrigeration cycles for liquefying low-boiling gaseous mixtures |
US3996030A (en) * | 1976-02-23 | 1976-12-07 | Suntech, Inc. | Fractionation of gases at low pressure |
US4054433A (en) * | 1975-02-06 | 1977-10-18 | L'air Liquide, Societe Anonyme Pour L'etude Et L'exploitation Des Procedes Georges Claude | Incorporated cascade cooling cycle for liquefying a gas by regasifying liquefied natural gas |
US4330307A (en) * | 1980-04-07 | 1982-05-18 | Coury Glenn E | Method of separating a noncondensable gas from a condensable vapor |
US4415345A (en) * | 1982-03-26 | 1983-11-15 | Union Carbide Corporation | Process to separate nitrogen from natural gas |
US4430103A (en) | 1982-02-24 | 1984-02-07 | Phillips Petroleum Company | Cryogenic recovery of LPG from natural gas |
US4680041A (en) * | 1985-12-30 | 1987-07-14 | Phillips Petroleum Company | Method for cooling normally gaseous material |
US4746342A (en) * | 1985-11-27 | 1988-05-24 | Phillips Petroleum Company | Recovery of NGL's and rejection of N2 from natural gas |
US5588306A (en) * | 1994-11-11 | 1996-12-31 | Linde Aktiengesellschaft | Process for obtaining an ethane-rich fraction for refilling an ethane-containing refrigerant circuit of a process for liquefaction of a hydrocarbon-rich fraction |
WO2002088612A1 (en) * | 2001-05-02 | 2002-11-07 | Linde Aktiengesellschaft | Method for separating nitrogen out of a hydrocarbon-rich fraction that contains nitrogen |
US6564578B1 (en) * | 2002-01-18 | 2003-05-20 | Bp Corporation North America Inc. | Self-refrigerated LNG process |
US20030136146A1 (en) * | 2002-01-18 | 2003-07-24 | Ernesto Fischer-Calderon | Integrated processing of natural gas into liquid products |
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US20050279132A1 (en) * | 2004-06-16 | 2005-12-22 | Eaton Anthony P | LNG system with enhanced turboexpander configuration |
US20050284176A1 (en) * | 2004-06-24 | 2005-12-29 | Eaton Anthony P | LNG system employing refluxed heavies removal column with overhead condensing |
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-
1969
- 1969-03-25 DE DE19691915218 patent/DE1915218B2/en active Granted
-
1970
- 1970-03-24 US US00022233A patent/US3721099A/en not_active Expired - Lifetime
- 1970-03-24 NL NL7004170A patent/NL7004170A/xx unknown
- 1970-03-25 FR FR7010733A patent/FR2035881B1/fr not_active Expired
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Also Published As
Publication number | Publication date |
---|---|
FR2035881B1 (en) | 1974-03-15 |
DE1915218C3 (en) | 1973-10-11 |
FR2035881A1 (en) | 1970-12-24 |
DE1915218B2 (en) | 1973-03-29 |
NL7004170A (en) | 1970-09-29 |
DE1915218A1 (en) | 1970-10-01 |
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