US2209748A - Method of separating the constituents of gaseous mixtures - Google Patents
Method of separating the constituents of gaseous mixtures Download PDFInfo
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- US2209748A US2209748A US222767A US22276738A US2209748A US 2209748 A US2209748 A US 2209748A US 222767 A US222767 A US 222767A US 22276738 A US22276738 A US 22276738A US 2209748 A US2209748 A US 2209748A
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- rectifier
- oxygen
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- air
- nitrogen
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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
- 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
Definitions
- Another object of the invention is to recover simultaneously with the oxygen a large fraction of the nitrogen in the air treated, in a high I degree of purity, with only a small amount of added expense.
- pipe Ii conveys the gaseous mixture to an exchanger i2 having compartmentsK and L, and thence through apipe it to the bottom of an auxiliary rectification column it.
- the liquid nitrogen collects in a bowl 34 from which it is withdrawn through a pipe 35 and delivered to the compartment M of an exchanger 38, wherein it is subjected to cooling by the gaseous efiiuent from the column escaping through a tube 31 and passing through the compartment N of the exchanger 36.
- the cold liquid is delivered through a valve 38 and pipe 391:0 the top of the rectifier l8 and serves as the reflux liquid for the rectification.
- a collector 53 indicated in dotted lines may be disposed in the auxiliary rectifier H to collect some of the nitrogen liquid descending from the tubes 22. This liquid may be delivered through a pipe 54, likewise indicated in dotted lines, and a valve 55, to the top of the rectifier l8.
- the efiluent from, the top of the auxiliary rectifier may be made to contain very large percentages of n ogen, ranging upward to 99.8 to 99.9% at slight additional cost. This process thus permits oxygen to be produced in commercial purity with a simple apparatus and low compression cost, while at the same time a large fraction of the nitrogen in the air treated may be recovered, if desired, in a high degree of. purity.
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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
y 30, 1940- J. L. SCHLITT METHOD OF SEBARATING THE CONSTITUENTS OF GASE OUS MIXTURES- Filed Aug. 5, I95
,1 1 i j i i 1 H 1 i l: EEE JE EE ll 5 INVENTOR Jade 54, L. Sw ng ATTO RNEYS Patented July 30, 1940 METHOD OF SEPARATING THE CONSTITU- ENTS OF GASEOUS MIXTURES Joseph L. Schlltt, Darien, Oonm, assignor to Air Reduction Company, Incorporated, New York, N. Y., a corporationot'liew York Application August 3, 1938, Serial No. 222,767
1 Claims; (oi. 432-1755) This invention relates to the separation of gaseous mixtures by liquefaction and rectification, and particularly to a method of treating air to recover the oxygen in an economical manner.
5 The liquefaction method of separating the constituents of air has been long established, but the commercial methods are subject to a number of defects and ineiiiclencies. These defects and inemciencies generally express themselves by relo quiring a relatively large .amount of power to separate air into its constituents.
It is the object of the present invention to provide a method which is emcient and economical whereby a high recovery of the oxygen in 1 the air treated is obtained in a simple manner and with the minimum cost of compression. At the same time, a method is provided which permits, if desired, the recovery of part of the nitrogen in any commercial degree of purity higher than the nitrogen product of any ordinary liquefaction system.
Another object of the invention is the provision of a method of separating the constituents of gaseous mixtures wherein numerous inemciencies oi the existing systems are avoided.
Another object of the invention is to recover simultaneously with the oxygen a large fraction of the nitrogen in the air treated, in a high I degree of purity, with only a small amount of added expense.
Other objects and advantages of the invention will be apparent as it is better understood by reference to the following specification and the accompanying drawing, which illustrates dia- '35 grammatically the apparatus which may be utilized in the practice of the method described.---
It will be understood that the drawing is merely illustrative and that details well known in the art have been omitted for the purpose of clarity. Referring to the drawing, an exchanger 5 is represented as comprising compartments A, B, C, D and E, and a similar exchanger 6 is similarly represented as comprising compartments F, G, H, I and J. The conventional arrangement can be used whereby heat exchange is efiected between the gases entering and leaving the apparatus. The entering gaseous mixture, for example air, is introduced in two parts. One part, initially compressed to a-pressure of for example 5 atmospheres absolute and cooled, is introduced through pipe 7 to the compartment 2B and passes thence through a pipe 8 and branch 5 to an expansion turbine it where the gaseous mixture is expanded to a pressure of for example 2 atmospheres absolute and thereby'cooled. A
pipe Ii conveys the gaseous mixture to an exchanger i2 having compartmentsK and L, and thence through apipe it to the bottom of an auxiliary rectification column it. Another portion of the air, compressed toa pressure of for 5 example ,2 atmospheres absolute and cooled, enters through a pipe It, passes through the compartment A of exchanger 5, thence through a pipe it to the compartment F of the exchanger 3, and is delivered by a'pipe it to the pipe it lo where it joins the air which has been expanded in the turbine it and is delivered to the bottom of the auxiliary rectifier it. A portion of the air entering the bottom of .the auxiliary rectifier it may be in the liquid i6 phase, and the liquid is augmented by oxygenenriched iiquid'delivered from the main rectifier it through a pipe it and valve 2d. The balance of the air passes upwardly through the auxiliary rectifier it and trays ti thereof in contact with '20 descending liquid produced as hereinafter described. The rectification efiected results in the accumulation 0! more liquid in the bottom of the rectifier in which liquid is enriched in oxygen, and a vapor principally nitrogen, which passes 25 up through condenser tubes 22 at the top of the auxiliary rectifier it. The tubes are partially surrounded by liquid supplied from the bottom of the rectifier through a pipe 28 and valve 24.
. The cooling of the vapor results in the provision 3c of a liquid containing nitrogen and oxygen and any other constituents oi the gaseous mixture which flows-downwardly over the trays 2! to eiiect the rectification already described. The
emuent, consisting of nitrogen of substantial 5 purity, i. e; upward to 99.9%. escapes "through a' pipe 25 and is delivered to the compartment L of theexchanger' 12. This nitrogeneflluent is still at the pressure of the auxiliaryrectifler and is expanded in a turbine 28 and thereby cooled. 40
It passes thence through a pipe 2'! to the compartment H oi the exchanger 6, and through apipe 28 to the compartment 0 of the exchanger 5. In the exchangers, the nitrogen serves to cool the incoming air. It is withdrawn through a 45 pipe 29 and conveyed to any suitable storage compartment for use as maybe required. Thus, the method affords immediately a quantity 01'. high purity nitrogen as one-of the products of the separation. 1 50 Another portion of the air at relatively high pressure is delivered to the compartment. G of the exchanger 6, and thence through a pipe-30 to the bottom of the rectifier i8. It passes up- I wardly through tubes 3! of a condenser, the tubes 55] products, with resulting liquefaction of the balance of the air which consists principally of nitrogen. The liquid nitrogen collects in a bowl 34 from which it is withdrawn through a pipe 35 and delivered to the compartment M of an exchanger 38, wherein it is subjected to cooling by the gaseous efiiuent from the column escaping through a tube 31 and passing through the compartment N of the exchanger 36. The cold liquid is delivered through a valve 38 and pipe 391:0 the top of the rectifier l8 and serves as the reflux liquid for the rectification.
The liquid flows downwardly over the trays 40 within the rectifier and is augmented by liquid delivered through a pipe 4| from the condenser at the top of the auxiliary rectifier M. The combined liquids flow downwardly over trays 42. The rectification results in the gradual enrichment of the liquid in oxygen and the accumulation of the nitrogen, a small portion of oxygen and other constituents of the atmosphere in the effluent which escapes through the pipe 31. The efiiuent, after passing through the compartment N of the exchanger 38, is delivered by a pipe 43 to the compartment Jof the exchanger 6, and thence through a'@ pipe 44 to the compartment E of the exchanger 5. It is withdrawn through a pipe 45 and delivered to the atmosphere as waste nitrogen.
The liquid which descends in the rectifier i8 accumulates in a receptacle 46 and overflows through a pipe 41' into the surrounding space. Some of the vapor from this liquid escapes through a pipe 8 and rises through the trays.
52 and delivered to any suitable storage receptacle. This vapor constitutes the oxygen product of the method. If it is desired to supply more reflux nitrogen liquid at the top of the rectifier l8, a collector 53 indicated in dotted lines may be disposed in the auxiliary rectifier H to collect some of the nitrogen liquid descending from the tubes 22. This liquid may be delivered through a pipe 54, likewise indicated in dotted lines, and a valve 55, to the top of the rectifier l8.
'From the above detailed description of the process it is seen that one portion of the air undergoes an initial separation, a feature common to many emcient air separation systems, into two liquid fractions, one containing substantially all of the oxygen in this portion of the air, the other being substantially pure nitrogen. The latter liquid fraction is used as reflux to the main column in the ordinary manner. The enriched oxygen liquid, however, is throttled to an intermediate pressure with the production of some vapor, and the other portion of the air treated is added thereto. The mixed vapor is subjected to a separate rectification wherein an efiluent is produced which-may be as pure nitrogen as is commercially demanded, and
'an oxygen enriched liquid fraction; The reflux for this auxiliary rectification is produced in a dephlegmator by evaporation" of a part of the oxygen enriched liquid throttled to the pressure prevailing outside the dephlegmator tubes. The
liquid and vapor mixture leaving the outside of the dephlegmator tubes is introduced to the main rectifier, operating at the lowest pressure in the rectification system, where it is then rectified in the usual manner by the reflux resulting from the initial separation of a part of the-air.
What has been accomplished by this procedure is that there has been introduced into the middle of the main rectifier a combined liquid and vapor stream containing substantially all of the oxygen in the treated air but considerably smaller in amount and much higher in oxygen composition than is ordinarily done. Therefore, less reflux is required at the top of the main rectifier and at the same time there is available from the top of the tubes of the dephlegmator a large portion of the nitrogen entering the system at a pressure considerably higher than exists in the main rectifier: This nitrogen under pressure is available for the production of refrigeration. The net result is a considerable decrease in the work of compression required to' maintain the necessary refrigeration in the system, and at the same time high recovery of the oxygen in all of the air treated is attained.
If desired, the efiluent from, the top of the auxiliary rectifier may be made to contain very large percentages of n ogen, ranging upward to 99.8 to 99.9% at slight additional cost. This process thus permits oxygen to be produced in commercial purity with a simple apparatus and low compression cost, while at the same time a large fraction of the nitrogen in the air treated may be recovered, if desired, in a high degree of. purity.
Various changes may be ma e in the procedure and particularly in the apparatus employed therefor, without departing from the invention or sacrificing any of the advantages thereof.
I claim:
1. The method of separating nitrogen and oxygen from the atmosphere by liquefaction and rectification which comprises compressing and cooling a portion of the air at relatively low pressure, compressing and cooling another portion at a relatively higher pressure, expanding a part of the air at relatively higher pressure, adding' the expanded air to the portion at lower pressure, rectifying the portion at the lower pressure with liquefied constituents thereof to separate the major portion of the nitrogen as a gaseous eiiluent of substantial purity, separating the portion at the relatively higher pressure into liquid fractions, rectifying such fractions after expansion with the liquid product of the first mentioned rectification, discarding the gaseous eilluent containing nitrogen, oxygen and other constituents of the atmosphere and evaporating the liquid 1 product to provide oxygen of substantial purity. 2. In the method of separating air into its main constituents,oxygen and nitrogen, in which the air is initially separated in a main rectifier into separation in them'ain rectifier, and admitting to an intermediate level of the main rectifier the oxygen-enriched mixed vapor and liquid resulting from said thermal contact in said auxiliary rectifier.
3. In the method of separating air into its mainriched fraction resulting from the initial separation in the main rectifier, withdrawing the uncondensed top product of the auxiliary rectifier as high purity nitrogen, andradmitting to an intermediate level of the main rectifier the oxygen-enriched mixed vapor and liquid resulting from said thermal contact in said auxiliary rectifier.
4. In the method of separating air into its main constituents, oxygen and nitrogen, in which the air is initially separated in a main rectifier into two liquid fractions in which oxygen and nitrogen, respectively, are concentrated; the improvement which comprises rectifying, in an auxiliary rectifier, a substantial additional quantity of gaseous unseparated air" with a portion of the top product of said rectification liquefied by thermalcontact with the oxygen-enriched product of the auxiliary rectifier mixed with the oxygen-enriched fraction resulting from the initial separationin the main rectifier, withdrawing the uncondensed top product of said auxiliary rectifier and expanding it for refrigeration purposes, and admitting to an intermediate level of the main rectifier the oxygen-enriched mixed vapor and liquid resulting from said thermal contact in said auxiliary rectifier. V
5. In the method of separating air into its main constituents, oxygen and nitrogen, in which the air is initially separated in a main rectifier into two liquid fractions in which oxygen and nitrogen, respectively, are concentrated; the improvement which comprises rectifying, in an aux Y iliary rectifier, a substantial additional quantity tion of the liquid produced at the top of the aux- I iliary rectifier to the top of the main rectifier to supplement the refiux liquid available in said main rectifier, and admitting to an intermediate level of I the main rectifier the oxygen-enriched mixed vapor and liquid resulting from said thermal contact insaid auxiliary rectifier.
6. In the method of separating air into its main constituents, oxygen and nitrogen, in which the air is initially separated in a main rectifier into two liquid fractions in which oxygen and nitrogen, respectively, are concentrated; the improvement which comprises expanding a substantial additional quantity of high pressure gaseous unseparated air to a lower pressure, rectifying said expanded air inan auxiliary rectifier with a. portion of the top product of said rectification liquefied by thermal contact with the oxygen-enriched product of the auxiliary rectifier mixed with the oxygen-enriched fraction resulting from the initial separation in the main rectifier, and admitting to an intermediate level of the main rectifier the oxygen-enriched mixed vapor and liquid resulting from said thermal contact in said auxiliary rectifier.
7. In the method of separatingair into its main constituents, oxygen and nitrogen, in which the air is initially separated in a main rectifier into two liquid fractions in which oxygen and nitrogen respectively are concentrated; the improvement which comprises rectifying, in an auxiliary rectifier, a substantial additional quantity of unseparated air with a portion of the top product of said rectification liquefied by thermal contact with the oxygen enriched fraction resulting from the initial rectification in the main rectifier, and admitting to an intermediate level of the main rectifier the oxygen. enriched mixed vapor and liquid resulting from said thermal contact in said auxiliary rectifier.
JOSEPH L. SCHLI'IT.
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US222767A US2209748A (en) | 1938-08-03 | 1938-08-03 | Method of separating the constituents of gaseous mixtures |
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US222767A US2209748A (en) | 1938-08-03 | 1938-08-03 | Method of separating the constituents of gaseous mixtures |
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Cited By (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2423273A (en) * | 1943-12-02 | 1947-07-01 | Air Reduction | Separation of the constituents of air |
US2527301A (en) * | 1943-08-04 | 1950-10-24 | Arthur J Fausek | Method of separating the constituents of gaseous mixtures |
US2620637A (en) * | 1946-10-09 | 1952-12-09 | Air Prod Inc | Air fractionating cycle and apparatus |
US2664719A (en) * | 1950-07-05 | 1954-01-05 | Union Carbide & Carbon Corp | Process and apparatus for separating gas mixtures |
US2709348A (en) * | 1949-05-20 | 1955-05-31 | Union Carbide & Carbon Corp | Process of and apparatus for separating gas mixtures |
US2716333A (en) * | 1946-04-11 | 1955-08-30 | Little Inc A | Method and means for treating gases |
US2716332A (en) * | 1950-04-20 | 1955-08-30 | Koppers Co Inc | Systems for separating nitrogen from natural gas |
US2729953A (en) * | 1946-10-09 | 1956-01-10 | Air Prod Inc | Air fractionating cycle and apparatus |
US2779174A (en) * | 1954-06-29 | 1957-01-29 | Air Liquide | Low temperature separation of gaseous mixtures |
US2850880A (en) * | 1955-01-05 | 1958-09-09 | Linde Eismasch Ag | Process and an apparatus for the separation of compressed air |
US2861432A (en) * | 1953-11-12 | 1958-11-25 | Haselden Geoffrey Gordon | Extraction of oxygen from the atmosphere and like operations |
US2867985A (en) * | 1953-07-15 | 1959-01-13 | Philips Corp | Gas-separating apparatus |
US2881595A (en) * | 1953-10-28 | 1959-04-14 | Air Prod Inc | Separation of gaseous mixtures |
US2915882A (en) * | 1955-05-31 | 1959-12-08 | British Oxygen Co Ltd | Separation of air |
US2940269A (en) * | 1956-01-04 | 1960-06-14 | Union Carbide Corp | Process and apparatus for separating gaseous mixtures by rectification |
US3100696A (en) * | 1957-07-04 | 1963-08-13 | Linde Eismasch Ag | Method and apparatus for separating gases |
US3264831A (en) * | 1962-01-12 | 1966-08-09 | Linde Ag | Method and apparatus for the separation of gas mixtures |
US3360944A (en) * | 1966-04-05 | 1968-01-02 | American Messer Corp | Gas liquefaction with work expansion of major feed portion |
US3683634A (en) * | 1968-08-24 | 1972-08-15 | Martin Streich | Prefractionation with subsequent recombination if feed in double column rectifier |
US4017284A (en) * | 1973-05-14 | 1977-04-12 | Cryox Corporation | Air distillation apparatus comprising regenerator means for producing oxygen |
US4254629A (en) * | 1979-05-17 | 1981-03-10 | Union Carbide Corporation | Cryogenic system for producing low-purity oxygen |
US4410343A (en) * | 1981-12-24 | 1983-10-18 | Union Carbide Corporation | Air boiling process to produce low purity oxygen |
US5337570A (en) * | 1993-07-22 | 1994-08-16 | Praxair Technology, Inc. | Cryogenic rectification system for producing lower purity oxygen |
US5582032A (en) * | 1995-08-11 | 1996-12-10 | Liquid Air Engineering Corporation | Ultra-high purity oxygen production |
-
1938
- 1938-08-03 US US222767A patent/US2209748A/en not_active Expired - Lifetime
Cited By (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2527301A (en) * | 1943-08-04 | 1950-10-24 | Arthur J Fausek | Method of separating the constituents of gaseous mixtures |
US2423273A (en) * | 1943-12-02 | 1947-07-01 | Air Reduction | Separation of the constituents of air |
US2716333A (en) * | 1946-04-11 | 1955-08-30 | Little Inc A | Method and means for treating gases |
US2620637A (en) * | 1946-10-09 | 1952-12-09 | Air Prod Inc | Air fractionating cycle and apparatus |
US2729953A (en) * | 1946-10-09 | 1956-01-10 | Air Prod Inc | Air fractionating cycle and apparatus |
US2709348A (en) * | 1949-05-20 | 1955-05-31 | Union Carbide & Carbon Corp | Process of and apparatus for separating gas mixtures |
US2716332A (en) * | 1950-04-20 | 1955-08-30 | Koppers Co Inc | Systems for separating nitrogen from natural gas |
US2664719A (en) * | 1950-07-05 | 1954-01-05 | Union Carbide & Carbon Corp | Process and apparatus for separating gas mixtures |
US2867985A (en) * | 1953-07-15 | 1959-01-13 | Philips Corp | Gas-separating apparatus |
US2881595A (en) * | 1953-10-28 | 1959-04-14 | Air Prod Inc | Separation of gaseous mixtures |
US2861432A (en) * | 1953-11-12 | 1958-11-25 | Haselden Geoffrey Gordon | Extraction of oxygen from the atmosphere and like operations |
US2779174A (en) * | 1954-06-29 | 1957-01-29 | Air Liquide | Low temperature separation of gaseous mixtures |
US2850880A (en) * | 1955-01-05 | 1958-09-09 | Linde Eismasch Ag | Process and an apparatus for the separation of compressed air |
US2915882A (en) * | 1955-05-31 | 1959-12-08 | British Oxygen Co Ltd | Separation of air |
US2940269A (en) * | 1956-01-04 | 1960-06-14 | Union Carbide Corp | Process and apparatus for separating gaseous mixtures by rectification |
US3100696A (en) * | 1957-07-04 | 1963-08-13 | Linde Eismasch Ag | Method and apparatus for separating gases |
US3264831A (en) * | 1962-01-12 | 1966-08-09 | Linde Ag | Method and apparatus for the separation of gas mixtures |
US3360944A (en) * | 1966-04-05 | 1968-01-02 | American Messer Corp | Gas liquefaction with work expansion of major feed portion |
US3683634A (en) * | 1968-08-24 | 1972-08-15 | Martin Streich | Prefractionation with subsequent recombination if feed in double column rectifier |
US4017284A (en) * | 1973-05-14 | 1977-04-12 | Cryox Corporation | Air distillation apparatus comprising regenerator means for producing oxygen |
US4254629A (en) * | 1979-05-17 | 1981-03-10 | Union Carbide Corporation | Cryogenic system for producing low-purity oxygen |
US4410343A (en) * | 1981-12-24 | 1983-10-18 | Union Carbide Corporation | Air boiling process to produce low purity oxygen |
US5337570A (en) * | 1993-07-22 | 1994-08-16 | Praxair Technology, Inc. | Cryogenic rectification system for producing lower purity oxygen |
US5582032A (en) * | 1995-08-11 | 1996-12-10 | Liquid Air Engineering Corporation | Ultra-high purity oxygen production |
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