US2659216A - Process for the separation of gas mixtures - Google Patents
Process for the separation of gas mixtures Download PDFInfo
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- US2659216A US2659216A US241938A US24193851A US2659216A US 2659216 A US2659216 A US 2659216A US 241938 A US241938 A US 241938A US 24193851 A US24193851 A US 24193851A US 2659216 A US2659216 A US 2659216A
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- heat exchange
- nitrogen
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- 239000000203 mixture Substances 0.000 title description 32
- 238000000034 method Methods 0.000 title description 25
- 238000000926 separation method Methods 0.000 title description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 34
- 239000007789 gas Substances 0.000 description 23
- 238000009835 boiling Methods 0.000 description 19
- 229910052757 nitrogen Inorganic materials 0.000 description 18
- 238000001816 cooling Methods 0.000 description 15
- 239000007788 liquid Substances 0.000 description 12
- 238000010992 reflux Methods 0.000 description 12
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 11
- 239000001301 oxygen Substances 0.000 description 11
- 229910052760 oxygen Inorganic materials 0.000 description 11
- 239000008246 gaseous mixture Substances 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 150000002829 nitrogen Chemical class 0.000 description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000000727 fraction Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052743 krypton Inorganic materials 0.000 description 1
- DNNSSWSSYDEUBZ-UHFFFAOYSA-N krypton atom Chemical compound [Kr] DNNSSWSSYDEUBZ-UHFFFAOYSA-N 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- 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
- F25J5/00—Arrangements of cold exchangers or cold accumulators in separation or liquefaction plants
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J3/00—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification
- F25J3/02—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
- F25J3/04—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 for air
-
- 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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S62/00—Refrigeration
- Y10S62/902—Apparatus
- Y10S62/909—Regeneration
Definitions
- the present invention relates to the separation of gas mixtures, and more particularly to those gas mixtures which are capable of giving a homogeneous liquid phase on cooling and of being separated into two or more fractions of different boiling points.
- Typical of such a gaseous mixture is air, and to facilitate an appreciation of the invention herein to be described, particular reference will be made to air separation,
- the nitrogen is liquefied by indirect heat-exchange with oxygen boiling at the base of a column operating at atmospheric pressure.
- the nitrogen is produced by partial rectification of the air in a column or similar apparatus operating at an elevated pressure, and, after liquefaction in the manner stated above, the liquid nitrogen is expanded to atmospheric pressure for use as refiux in the main column.
- nitrogen may be produced in an auxiliary apparatus,
- an enricher as described in British Patent No. 632,329 or may be withdrawn from the top of the main column at atmospheric pressure in gaseous form. It is then compressed to an elevated pressure such that it may be liquefied by heat exchange with the oxygen in the base of the main column as hereinbefore described.
- a method of separating a gas mixture into a lower boiling point fraction and at least one fraction of higher boiling point comprising the steps of compressing the gas mixture, cooling the compressed gas mixture to a saturated vapour by heat exchange with at least part of the fraction produced, condensing at least part of this vapour by heat exchange with the boiling highest-boiling fraction, using at least part of this condensed mixture for liquefying vapour to provide refiux medium, recompressing the evaporated mixture to at least atmospheric pressure, cooling and expanding this recompressed gas mixture to saturation point, separating a stream of the gas mixture into the aforementioned fractions by 11 Claims. (Cl. 62-1755) countercurrent contact in a rectification device with the reflux medium and recovering from all cold vapours the cold used for cooling the incoming gas stream.
- the reflux medium for the rectification device may be provided by a part of the separated lower boiling fraction, liquefied by indirect heat exchange with the condensed gaseous mixture.
- the upper portion of the rectification column is formed as an enricher wherein the vapours rich in the lower boiling point constituent are condensed to form the reflux medium by indirect heat exchange with the condensed gas mixture.
- This method makes it possible to use already known methods of heat exchange and of purification of the incoming gas mixture from condensible impurities.
- the extra cold necessary to balance losses by heat leak, and other well-known losses, may also be obtained by any conventional means, for example, by expansion of gas in a turbine or other expansion engine.
- the rectification device may conveniently operate at substantially atmospheric pressure (in which case the liquid/gas mixture evaporates under reduced pressure) or at an elevated pressure such that the liquid/gas-mixture evaporates at substantially atmospheric pressure.
- regenerators are shown for cooling the compressed air.
- a pair of associated regenerators bear the same reference numeral and the members of each pair are marked respectively by the suffix a or b, the sufiix a being applied to the cooling regenerator and the sufiix b to the regenerator which is in course of being cooled.
- air is compressed in a turbo-compressor l to approximately '70 p. ;s i. .a. and cooled to saturation point ,by counter-current heat exchange with the separatednitrogen frac tion in one pair of regenerators ,Za, Zb tt-he suflix a being applied to the cooling regenerator and the suflix b to that being-cooled). It is then completely condensed by indirect heat exchange with the oxygen boiling at the base of the separation column 3. I The liquid air is then sub-cooled in sub-cooler 4 "by heat exchangewith nitrogen from the-top of the column :3 and--with low-pressure evaporated air produced as hereafter described.
- the sub-cooled liquid --- is expanded through Valve to approximately '7 p. s; i. a. and evaporated by indirect heat exchange in exchanger 6 with part or the nitrogen from the top of the column, condensing this nitrogen which is returned to the column as reflux.
- the evaporated air is warmed slightly insub-cooling the liquid air sub-cooler 4 and is then warmed to substantially atmospheric temperature by heat exchange with incoming air in a second pair of regenerators la, 1b.
- the low-pressure air is recompressed to approximately '35 p. s. i. a. in two stages in turbo-compressor 8, more air at atmospheric pressure being added after the first stage and compressed within the secondstage.
- this intermediate pressure air is thencooled countercurrent to the low pressure air in regenerators la, lb; the remainder is cooled countercurrent to the oxygen stream from the base of the column in regenerators 9a, 91). All the intermediate pressure air is then further cooled by heat exchange with the nitrogen stream from sub-cooler 4 in exchanger i0. This-step does not eliminate the necessity'for super-heating the air before it enters the turbine.
- the nitrogen stream maybe warmed by cooling an air stream used for balancing the regenerators (not shown in the figure) This nitrogen stream then passes to the regenerators 2a, 2b.
- the intermediate pressure air then passes through expansion turbine ll, being thus cooled to saturation point and issuing from the turbine H at the column pressure; it then enters column 3 at the appropriate point as a gaseous feed.
- FIG. 2 The arrangement shown in Figure 2 is substantially similar to that in Figure 1, with the exception that the exchanger 6 is replaced by an enricher l2 at the top of the column 3.
- the liquid air after expansion through valve 5 to a pressure of approximately 12 p. s. i. a. is passed through the enricher i2 where it acts to condense vapours rich in nitrogen to form the refluxfor the column .3.
- Figure 3 shows an arrangement similar to that shown in Figure 1, except that in this case only a part of the sub-cooled liquid air is expanded through valve 5 to the exchanger 6, the remainder "being expanded through valve l3 to substantially gatmospheric pressure and introduced into the column 3 as liquid feed.
- Figure 4 shows an arrangement providing for a liquid feed to column 3 as in the arrangement shown in Figure 3, combined with the use of an enricher I2 as previously described with reference to Figure 2.
- the second pair of regenerators 8a, 8b maybe eliminated, and the low-pressure air passed direct to a jet-pump after evaporation.
- the driving fluid for this pump is obtained as side-stream from the first pair of regenerators 2a, 2b in known manner.
- This side stream passes through an expansion turbine, being thus cooled to saturation point, and issues ,at the pressure necessary to operate the jet pump.
- Thedelivery of the pump is at .substantially column temperature and is introduced into the column .as gaseous feed.
- theoxygen fraction produced by any of the methods above described may, if desired, .be further separated to produce an argon-enriched. fraction, substantially pure oxygen, and/or a fraction enriched in krypton and xenon.
- a method of separating a gas mixture into a lower boiling point fraction and at least one fraction of higher boiling point which comprises the steps of compressing the gas mixture, cooling the compressed gas mixture to form a saturated vapour by heat exchange with at least part of the fractions produced, condensing at least .part or this vapour by heat exchange with the boiling highest-boiling fraction, expanding this condensed mixture and using at least part thereof for liquefying vapour to provide reflux medium, recompressing the evaporated mixture to at least atmospheric pressure, .cooling and expanding this recompressed gas mixture to saturation point, separating a stream of thegas mixture into the aforementioned fractions by countercurrent contact in a rectification device with the said reflux medium, and recovering from all cold vapours the cold used for cooling the incoming stream of gas mixture.
- the rectification device comprises a rectification column surmounted by an enricher wherein the vapours rich in the lower boiling point constituent are condensed to serve as reflux medium in the column by indirect heat exchange with the o den ed seou xt r i e d accordin to aim 1 whe only a part of the condensed mixture is used for liquefying the lower boiling point fraction, the remainder after expansion to the column pressure being fed to the rectification column at an appropriate point as a liquid feed. 5
- a method of separating air into a nitrogen 1 fraction and an oxygen fraction which comprises the steps of compressing the air, cooling the compressed air to form a saturated vapour by heat exchange with at least one of the fractions produced, condensing at least part of this vapour 1 by heat exchange with the boiling oxygen fraction, expanding this condensed vapour and using at least part thereof for liqueiying vapour to serve as reflux medium, re-compressing the evaporated air to at least atmospheric pressure, 20
- the rectification device comprises a rectification column surmounted by an enricher wherein the vapours rich in nitrogen are condensed toserve as reflux medium in the column by indirect heat exchange with the condensed air.
- a method according to claim 6 wherein the evaporated air prior to recompression is used to cool the recompressed air in alternating heat exchangers and wherein a relatively pure tail fraction of the evaporated air leaving the alternating heat exchanger is used after recompression to cool the separated oxygen fraction.
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- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Mechanical Engineering (AREA)
- Thermal Sciences (AREA)
- General Engineering & Computer Science (AREA)
- Separation By Low-Temperature Treatments (AREA)
Description
Nov. 17, 1953 R. w. H. SARGENT 2,659,216
PROCESS FOR THE SEPARATION OF GAS MIXTURES -Filed Aug. 15, 1951 4 Sheets-Sheet l mrkoaav Inventor oger H.o.v e
Nov. 17, 1953 7R. w. H SARGENT 2,659,216
' PROCESS FOR THE SEPARATION OF GAS MIXTURES Filed Aug. 15, 1951 4 Sheets-Sheet 2 Inventor 7, 1953 R. w. H. SARGENT PROCESS FOR THE SEPARATION OF GAS MIXTURES 4 Sheets-Sheet 3 Filed Aug. 15, 1951 l nvenh n R 05 ev W; ave w c2 Q1 A Home y Nov. 17, 1953 R. w. H. SARGENT PROCESS FOR THE SEPARATION OF GAS MIXTURES 4 Sheets-Sheet 4 Filed Aug. 15, 1951 Attorney Patented Nov. 17,
PROCESS FOR THE SEPARATION OF GAS MIXTURES Roger William Herbert Sargent, London, England, assignor to The British Oxygen Company Limited, London, England, a British company Application August 15, 1951, Serial No. 241,938
1 The present invention relates to the separation of gas mixtures, and more particularly to those gas mixtures which are capable of giving a homogeneous liquid phase on cooling and of being separated into two or more fractions of different boiling points. Typical of such a gaseous mixture is air, and to facilitate an appreciation of the invention herein to be described, particular reference will be made to air separation,
Previous methods of producing both oxygen and nitrogen in a substantially pure state fall into two classes; the use of the well-known dou his column, and methods using an auxiliary nitrogen circuit, with recompression of the nitrogen.
In both cases however the nitrogen is liquefied by indirect heat-exchange with oxygen boiling at the base of a column operating at atmospheric pressure. In the first case, the nitrogen is produced by partial rectification of the air in a column or similar apparatus operating at an elevated pressure, and, after liquefaction in the manner stated above, the liquid nitrogen is expanded to atmospheric pressure for use as refiux in the main column. In the second case, nitrogen may be produced in an auxiliary apparatus,
for example an enricher as described in British Patent No. 632,329 or may be withdrawn from the top of the main column at atmospheric pressure in gaseous form. It is then compressed to an elevated pressure such that it may be liquefied by heat exchange with the oxygen in the base of the main column as hereinbefore described.
It is an object of the present invention to provide a method for the separation of a gas mixture into a lower boiling point fraction and at least one higher boiling point fraction which uses a single rectification column and in which the lower boiling point fracton is at no time compressed to a higher pressure than that of the column.
There is thus provided by the present invention a method of separating a gas mixture into a lower boiling point fraction and at least one fraction of higher boiling point, comprising the steps of compressing the gas mixture, cooling the compressed gas mixture to a saturated vapour by heat exchange with at least part of the fraction produced, condensing at least part of this vapour by heat exchange with the boiling highest-boiling fraction, using at least part of this condensed mixture for liquefying vapour to provide refiux medium, recompressing the evaporated mixture to at least atmospheric pressure, cooling and expanding this recompressed gas mixture to saturation point, separating a stream of the gas mixture into the aforementioned fractions by 11 Claims. (Cl. 62-1755) countercurrent contact in a rectification device with the reflux medium and recovering from all cold vapours the cold used for cooling the incoming gas stream.
The reflux medium for the rectification device may be provided by a part of the separated lower boiling fraction, liquefied by indirect heat exchange with the condensed gaseous mixture. Alternatively, the upper portion of the rectification column is formed as an enricher wherein the vapours rich in the lower boiling point constituent are condensed to form the reflux medium by indirect heat exchange with the condensed gas mixture.
This method makes it possible to use already known methods of heat exchange and of purification of the incoming gas mixture from condensible impurities.
The extra cold necessary to balance losses by heat leak, and other well-known losses, may also be obtained by any conventional means, for example, by expansion of gas in a turbine or other expansion engine.
The rectification device may conveniently operate at substantially atmospheric pressure (in which case the liquid/gas mixture evaporates under reduced pressure) or at an elevated pressure such that the liquid/gas-mixture evaporates at substantially atmospheric pressure.
The invention as applied to the separation of air will now be described in more detail with reference to Figures 1 to 4 of the accompanying drawings which show diagrammatically four methods of carrying the invention into effect. Like parts in all figures bear the same reference numeral. The direction of flow along the interconnecting pipework is everywhere shown by arrows.
In all the figures, regenerators are shown for cooling the compressed air. In all figures a pair of associated regenerators bear the same reference numeral and the members of each pair are marked respectively by the suffix a or b, the sufiix a being applied to the cooling regenerator and the sufiix b to the regenerator which is in course of being cooled.
To avoid undue elaboration of the description several features for carrying the process into effeet which are well known per se to those skilled in the art have been omitted from the drawings. It will be appreciated, for example, that in practice there will have to be provision for removing residual traces of moisture and carbon dioxide from the cooled mixture emerging from the recondensed gases before expansion; that vapours must be superheated before isentropic expansion; that the gas flows through a pair of associated regenerators must be balanced to ensure the attaimnent of the required thermal conditions and the complete remoyal of condensates; also that a change=over valve mechanism has to be pro vided for sets of associated regenerators. All such features are well known and have been omitted in the interests of simplicity.
Referring to Fig. 1, air is compressed in a turbo-compressor l to approximately '70 p. ;s i. .a. and cooled to saturation point ,by counter-current heat exchange with the separatednitrogen frac tion in one pair of regenerators ,Za, Zb tt-he suflix a being applied to the cooling regenerator and the suflix b to that being-cooled). It is then completely condensed by indirect heat exchange with the oxygen boiling at the base of the separation column 3. I The liquid air is then sub-cooled in sub-cooler 4 "by heat exchangewith nitrogen from the-top of the column :3 and--with low-pressure evaporated air produced as hereafter described. The sub-cooled liquid ---is expanded through Valve to approximately '7 p. s; i. a. and evaporated by indirect heat exchange in exchanger 6 with part or the nitrogen from the top of the column, condensing this nitrogen which is returned to the column as reflux. The evaporated air is warmed slightly insub-cooling the liquid air sub-cooler 4 and is then warmed to substantially atmospheric temperature by heat exchange with incoming air in a second pair of regenerators la, 1b. The low-pressure air is recompressed to approximately '35 p. s. i. a. in two stages in turbo-compressor 8, more air at atmospheric pressure being added after the first stage and compressed within the secondstage. Part of this intermediate pressure air is thencooled countercurrent to the low pressure air in regenerators la, lb; the remainder is cooled countercurrent to the oxygen stream from the base of the column in regenerators 9a, 91). All the intermediate pressure air is then further cooled by heat exchange with the nitrogen stream from sub-cooler 4 in exchanger i0. This-step does not eliminate the necessity'for super-heating the air before it enters the turbine. Alternatively, the nitrogen stream maybe warmed by cooling an air stream used for balancing the regenerators (not shown in the figure) This nitrogen stream then passes to the regenerators 2a, 2b. The intermediate pressure air then passes through expansion turbine ll, being thus cooled to saturation point and issuing from the turbine H at the column pressure; it then enters column 3 at the appropriate point as a gaseous feed.
Condensible impurities in the incoming air are deposited in both pairs of regenerators 2a., 2b and "la, 1b and subsequently re-evaporated into the out-going streams. It has been found that in viewof the difference in actual volumes between the incoming air stream and the outgoing air stream passing through regenerators la, "lib, substantially the whole of the condensates in the regenerators will have been revaporised by the outgoing air stream well before the end of the cycle. The cold low-pressure air leaving the regenerator during the concluding part of the cycle will in consequence be substantially free from revaporised condensates and advantage can be taken of this phenomenon to efiect removal of cold from the oxygen stream. Since the tail portion contains no condensible impurities, any convenient type of exchanger can be used, without danger of blocking the exchanger by the accumulation of deposits or of contaminating the oxygen.
The arrangement shown in Figure 2 is substantially similar to that in Figure 1, with the exception that the exchanger 6 is replaced by an enricher l2 at the top of the column 3. The liquid air after expansion through valve 5 to a pressure of approximately 12 p. s. i. a. is passed through the enricher i2 where it acts to condense vapours rich in nitrogen to form the refluxfor the column .3.
Figure 3 shows an arrangement similar to that shown in Figure 1, except that in this case only a part of the sub-cooled liquid air is expanded through valve 5 to the exchanger 6, the remainder "being expanded through valve l3 to substantially gatmospheric pressure and introduced into the column 3 as liquid feed.
Figure 4 shows an arrangement providing for a liquid feed to column 3 as in the arrangement shown in Figure 3, combined with the use of an enricher I2 as previously described with reference to Figure 2.
In any of the cycles shown in the figures, the second pair of regenerators 8a, 8b maybe eliminated, and the low-pressure air passed direct to a jet-pump after evaporation. The driving fluid for this pump is obtained as side-stream from the first pair of regenerators 2a, 2b in known manner. This side stream passes through an expansion turbine, being thus cooled to saturation point, and issues ,at the pressure necessary to operate the jet pump. Thedelivery of the pump is at .substantially column temperature and is introduced into the column .as gaseous feed.
It .will be understood that theoxygen fraction produced by any of the methods above described, may, if desired, .be further separated to produce an argon-enriched. fraction, substantially pure oxygen, and/or a fraction enriched in krypton and xenon.
I claim:
1. A method of separating a gas mixture into a lower boiling point fraction and at least one fraction of higher boiling point which comprises the steps of compressing the gas mixture, cooling the compressed gas mixture to form a saturated vapour by heat exchange with at least part of the fractions produced, condensing at least .part or this vapour by heat exchange with the boiling highest-boiling fraction, expanding this condensed mixture and using at least part thereof for liquefying vapour to provide reflux medium, recompressing the evaporated mixture to at least atmospheric pressure, .cooling and expanding this recompressed gas mixture to saturation point, separating a stream of thegas mixture into the aforementioned fractions by countercurrent contact in a rectification device with the said reflux medium, and recovering from all cold vapours the cold used for cooling the incoming stream of gas mixture.
2. A method according to claim 1 wherein the reflux medium ior'the rectification device is provided by apart of the separated lower boilin point fraction liquefied by indirect heat exchange with the condensed gaseous mixture.
3. A method according to claim 1 wherein the rectification device comprises a rectification column surmounted by an enricher wherein the vapours rich in the lower boiling point constituent are condensed to serve as reflux medium in the column by indirect heat exchange with the o den ed seou xt r i e d accordin to aim 1 whe only a part of the condensed mixture is used for liquefying the lower boiling point fraction, the remainder after expansion to the column pressure being fed to the rectification column at an appropriate point as a liquid feed. 5
5. A method according to claim 1 wherein the evaporated mixture prior to re-compression is used to cool the i e-compressed gas mixture in alternating heat exchangers.
6. A method of separating air into a nitrogen 1 fraction and an oxygen fraction which comprises the steps of compressing the air, cooling the compressed air to form a saturated vapour by heat exchange with at least one of the fractions produced, condensing at least part of this vapour 1 by heat exchange with the boiling oxygen fraction, expanding this condensed vapour and using at least part thereof for liqueiying vapour to serve as reflux medium, re-compressing the evaporated air to at least atmospheric pressure, 20
cooling and expanding the re-compressed air to saturation point, separating a stream of the air into the aforementioned fractions by countercurrent contact in a rectification device with the said reflux medium, and recovering from all 25 cold vapours the cold used for cooling the incoming stream of air.
7. A method according to claim 6 wherein the reflux medium for the rectification device is provided by a. part of the separated nitrogen frac- 30 tion liquefied by indirect heat exchange with the condensed air.
8. A method according to claim 6 wherein the rectification device comprises a rectification column surmounted by an enricher wherein the vapours rich in nitrogen are condensed toserve as reflux medium in the column by indirect heat exchange with the condensed air.
9. A method according to claim 6 wherein only a part of the condensed air is used for liquefying the nitrogen fraction, the remainder after expansion to the column pressure being fed to the rectification column at an appropriate point as a liquid feed.
10. A method according to claim 6 wherein the evaporated air prior to re-oompression is used to cool the re-compressed air in alternating heat exchangers.
11. A method according to claim 6 wherein the evaporated air prior to recompression is used to cool the recompressed air in alternating heat exchangers and wherein a relatively pure tail fraction of the evaporated air leaving the alternating heat exchanger is used after recompression to cool the separated oxygen fraction.
ROGER WILLIAM HERBERT SARGENT.
References Cited in the file of this patent UNITED STATES PATENTS Number
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US241938A US2659216A (en) | 1951-08-15 | 1951-08-15 | Process for the separation of gas mixtures |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US241938A US2659216A (en) | 1951-08-15 | 1951-08-15 | Process for the separation of gas mixtures |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2659216A true US2659216A (en) | 1953-11-17 |
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ID=22912801
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US241938A Expired - Lifetime US2659216A (en) | 1951-08-15 | 1951-08-15 | Process for the separation of gas mixtures |
Country Status (1)
| Country | Link |
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| US (1) | US2659216A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3100696A (en) * | 1957-07-04 | 1963-08-13 | Linde Eismasch Ag | Method and apparatus for separating gases |
| US3143406A (en) * | 1957-07-04 | 1964-08-04 | Linde Eismasch Ag | System for conducting heat exchange operations in a gas separation apparatus incorporating periodically reversible regenerators |
| US3251189A (en) * | 1960-04-14 | 1966-05-17 | Linde Eismaschinen Ag | Gas separation process and apparatus |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2495549A (en) * | 1949-03-15 | 1950-01-24 | Elliott Co | Separation of ternary gaseous mixtures containing hydrogen and methane |
-
1951
- 1951-08-15 US US241938A patent/US2659216A/en not_active Expired - Lifetime
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2495549A (en) * | 1949-03-15 | 1950-01-24 | Elliott Co | Separation of ternary gaseous mixtures containing hydrogen and methane |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3100696A (en) * | 1957-07-04 | 1963-08-13 | Linde Eismasch Ag | Method and apparatus for separating gases |
| US3143406A (en) * | 1957-07-04 | 1964-08-04 | Linde Eismasch Ag | System for conducting heat exchange operations in a gas separation apparatus incorporating periodically reversible regenerators |
| US3251189A (en) * | 1960-04-14 | 1966-05-17 | Linde Eismaschinen Ag | Gas separation process and apparatus |
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