US1967717A - Process for purifying liquefied gases - Google Patents
Process for purifying liquefied gases Download PDFInfo
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- US1967717A US1967717A US607032A US60703232A US1967717A US 1967717 A US1967717 A US 1967717A US 607032 A US607032 A US 607032A US 60703232 A US60703232 A US 60703232A US 1967717 A US1967717 A US 1967717A
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- liquid
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- 239000007789 gas Substances 0.000 title description 40
- 238000000034 method Methods 0.000 title description 18
- 239000012535 impurity Substances 0.000 description 38
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 27
- 239000007788 liquid Substances 0.000 description 27
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 20
- 239000001301 oxygen Substances 0.000 description 20
- 229910052760 oxygen Inorganic materials 0.000 description 20
- 238000004519 manufacturing process Methods 0.000 description 16
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 14
- 239000007791 liquid phase Substances 0.000 description 13
- 238000009835 boiling Methods 0.000 description 12
- 239000012071 phase Substances 0.000 description 12
- 238000010438 heat treatment Methods 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 230000008018 melting Effects 0.000 description 7
- 238000002844 melting Methods 0.000 description 7
- 229910052757 nitrogen Inorganic materials 0.000 description 7
- 238000001704 evaporation Methods 0.000 description 6
- 238000005192 partition Methods 0.000 description 5
- 238000010992 reflux Methods 0.000 description 5
- 238000004821 distillation Methods 0.000 description 4
- 230000008020 evaporation Effects 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000009833 condensation Methods 0.000 description 3
- 230000005494 condensation Effects 0.000 description 3
- 239000002826 coolant Substances 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 238000000746 purification Methods 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 238000007599 discharging Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 206010022000 influenza Diseases 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 230000008016 vaporization Effects 0.000 description 2
- 239000006200 vaporizer Substances 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000005057 refrigeration Methods 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
Images
Classifications
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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
- F25J3/04406—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 using a dual pressure main column system
- F25J3/0443—A main column system not otherwise provided, e.g. a modified double column flowsheet
-
- 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
- F25J3/04763—Start-up or control of the process; Details of the apparatus used
- F25J3/04866—Construction and layout of air fractionation equipments, e.g. valves, machines
- F25J3/04896—Details of columns, e.g. internals, inlet/outlet devices
- F25J3/04933—Partitioning walls or sheets
-
- 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
- F25J2200/00—Processes or apparatus using separation by rectification
- F25J2200/50—Processes or apparatus using separation by rectification using multiple (re-)boiler-condensers at different heights of the column
- F25J2200/52—Processes or apparatus using separation by rectification using multiple (re-)boiler-condensers at different heights of the column in the high pressure column of a double pressure main column system
-
- 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
- F25J2200/00—Processes or apparatus using separation by rectification
- F25J2200/50—Processes or apparatus using separation by rectification using multiple (re-)boiler-condensers at different heights of the column
- F25J2200/54—Processes or apparatus using separation by rectification using multiple (re-)boiler-condensers at different heights of the column in the low pressure column of a double pressure main column system
Definitions
- This invention relates to a process and apparatus for purifying liquefied gases, particularly liquefied gases having low boiling points, such as liquid oxygen, nitrogen, and the like,
- the invention relates to the provision of suitable steps for concentrating undesired impurities occurring -in the production of liquefied gases of the character indicated in a manner in the cycle. of production such that the impurities may be separated readily by mechanical means, whereby a gas product is finally obtained in the liquid phase from which substantially all I impurities are practically completely removed.
- Another object is to produce a liquefied gas in a purified condition with an expenditure of a relatively small amount of additional energy and at relatively little additional cost.
- Still another object is to separate the desired liquefied gas from the undesired impurity by the step either of partial evaporation or partial condensation and thereafter causing the gas material to revert to the liquid phase with an expenditure of a relatively small amount of energy.
- Fig. i is a view mainly in vertical cross section showing a simple form of apparatus adapted for carrying out the process of the present invention.
- Fig. 2. is a view mainly in vertical section showing a gas production apparatus incorporating purifying apparatus arranged for the prac tice of the present invention.
- the purification may be accomplished with the expenditure o1 relatively little energy by taking the gas material in the liquid phase and treating it by the step of partial evaporation to produce two phases and then separating the phases.
- Such a process is generically set forth in the copending application filed in the name of Lawrence J. Bowditch on April 23, 1932, Serial No. 607,074, where 6 it is proposed to remove those impurities which occur in relatively small amounts in liquefied gases such as liquid air, oxygen, and the like, the concentration they do not materi carbon dioxide, being such that ally change the boiling point of the liquefied gas, but are otherwise objectionable and impair the commercial qualities of the gas product.
- step of condensation in order liquefied gas such as liquid oxygen in substantially pure condition, this step being preferably practiced so as to the condensation by product from another production.
- FIG. l A denotes generally accomplish the utilization of a byportion of the cycle of to the drawings, and particue a part of the apparatus into which the gas material in liquid phase that is to be purified is passed and caused to evaporate partially by the application of heat,
- the vaporizing portion of part A consists of a vessel 10 having an inlet conduit 11 for the liquefied gas, an outlet conduit 12 for the vapor, and a drain conduit 13 with a control valve 13
- a suitable heating means for example a coil 14 provided with inlet and outlet connections adapted to be supplied with a heating agent.
- This agent may be any convenient vehicle that will pass without difficulty at thelow operating temperatures here employed, for example, compressed air.
- the vapor outlet. conduit 12 surrounds the inlet conduit 11 in order to effect heat exchange and separation of the liquid from the gas phase; the vapor thus separated being led from the top of the evaporating vessel 10 over refluxing means to the condenser.
- the condenser shown in connection with part B consists of an upper header 15 and a lower header 16 connected by condenser tubes 17.
- the conduit 12 is here shown as discharging the vapor to be condensed into the upper header 15, while a conduit 18 is connected to the lower header to withdraw the reliquefied gas.
- the condenser is disposed within a chamber 19 having inlet and outlet conduits 20 and 21, respectively, for the purpose of circulating a cooling medium, for example, liquefied oxygen, or a cold gaseous material that may be a by-prodnot drawn from another part of the manufacturing cycle; the cooling medium carrying away the heat from the condenser so that re-liquefaction is readily accomplished in the condenser.
- a cooling medium for example, liquefied oxygen, or a cold gaseous material that may be a by-prodnot drawn from another part of the manufacturing cycle
- the vapor is conducted through conduit 12 into the condenser at its upper header 15 whence it passes into the tubes 17 and is condensed because it loses heat through the tube walls to the fluid of lower temperature surrounding the tubes.
- the liquefied gas collects in the lower header 16 from which it is withdrawn through conduit 18 in a punfied state.
- a heat interchanger for the manufacture of liquefied oxygen is modified and arranged to separate out the impurities which have relatively high boiling points and are in general inflammable, and then recondense the purified oxygen in order to supply it in the liquid phase.
- a conduit 25 provided with an expansion valve 26 is arranged to supply compressed air drawn from a suitable high pressure source to the rectifying column shown generally at 27.
- This rectifying column is-provided with a K61;-
- a conduit 30 provided with an expansion valve 31 and distributor 32 is arranged to draw liquid from the evaporator 28 and to discharge it into the upper portion of a second rectifying column 33 disposed above the column 2'? and arranged to be in heat exchanging relation with the condenser 29.
- Each of these columns is provided with suitable counter-current contact cooling means, for example, a series of perforated trays, as shown at 2'7 in the column 27 and at 33 in the column 33.
- the evaporator 28 associated with the column 27 is provided with suitable heating means, for example a heating coil as shown at 28'.
- a tray 27 arranged to collect the condensate which drips from the condenser 29 and to convey the same to a conduit 34 having a controlling valve 35 and 'a distributor 36 discharging into the top of the column 33, the distributor 36 being preferably disposed above the distributor 32.
- a gas withdrawal conduit 37 which is arranged for withdrawing non-condensible vapors, while a liquid withdrawal conduit 38 is arranged to withdraw liquid from the .base of the column 33 from about the condenser From this arrangement, it is seen that the compressed air introduced into the column 27 is liquefied by the passage through the expansion valve 26 and through the trays 27'; the liquid collecting in the evaporator 28. Gas or vapor rising through the column 2'? passes into the condenser 29 where the less volatile portion is recondensed and produces a reflux in the column 27. Liquid nitrogen collects in the tray 27", whereas the liquid in the evaporator 28 comprises a relatively large percentage 'of liquid oxygen.
- Any non-condensible vapor that is more volatile than liquid nitrogen or oxygen is withdrawn through the conduit 37.
- Liquefied gas comprising mainly liquid oxygen and'the impurities of relatively high melting point are withdrawn through the conduit 30 and introduced into the column 33 through the distributor 32.
- a second condenser shown generally at 40 is incorporated at a point in the column 33 where the vapor pressure of the undesired impurity is negligible.
- This condenser comprises upper and lower portions 41 and 42, connected by an inter- One or more passages or flues 44 are associated with the condenser in order to establish communication between the space above the condenser with the space below; a chamber for this condenser being preferably provided in the column by means of a partition 45 disposed transversely in the column below the condenser and a second partition 46, which is disposed above the condenser.
- This chamber occupies a space normally occupied by refluxing means such as counter-current contact cooling trays, and preferably has trays both above and belowthe same, those shown below being -denoted 33".
- the partition 46 is provided with one or more passages 47 that permits communication with the flues 44 so as to establish communication in the column 33 for the space on the two sides of the condenser chamber containing condenser 40.
- the partition 46 is also provided with one or more liquid drains 48 which allow liquid to drain from the partition into the chamber about the condenser 40.
- Gaseous oxygen to be recondensed and'which has been evaporated by the condenser 29- is led from a. point near the lower end of the column 33 from the chamber about the condenser 29 by means of a conduit 50 and passed into the portion 41 of condenser 40.
- liquid oxygen collects in a purified state and is withdrawn from the lower portion 42 through a conduit 51.
- the heat absorbed from the condenser 29 in effecting refrigeration for the column 2'7 vaporizes a portion of the liquid which is now a high concentrate of liquid oxygen contaminated with the impurities of relatively high melting point.
- the oxygen vaporized in this chamber is substantially pure oxygen gas which is *withdrawn through the conduit 50 and passed into the condenser 40, where it is recondensed bythe heatabstracted by the liquid in the chamber about the condenser 40.
- the liquid which collects in the chamber about the condenser 40 is seen to comprise a mixture of oxygen and nitrogen in the liquid phases, together with any substances that may be present either as solids or in solution.
- the vaporization which takes place in this chamber is of a fractional nature, the more volatile nitrogen being boiled oif and passed up through the fiues 47 into the upper portion of the column 33.
- This liquid nitrogen is seen to be supplied to the column mainly from the conduit 34; thus the cooling of the condenser 40 is seen to be accomplished by means of a cooling agent that is withdrawn from another portion of the cycle of production.
- the vaporized nitrogen is seen to pass from the top of the column 33 in the usual manner.
- the agents here used for heating the liquid in the evaporators and for extracting heat from the vapor in the condensers, in order to con; serve energy, are thus with advantage both taken from some other portions of the cycle of production, and since no change has occurred therein otherthan a change in the quantity of absorbed heat, they may be returned, if desired, to the cycle substantially without loss.
- the process of removing inflammable impurities from oxygen during the commercial production of liquid oxygen comprises collecting oxygen substantially in the liquid'phase and containing the undesired impurity, said impurity occurring in the collected liquid oxygen at a concentration such that the boiling point of the liquid oxygen is not substantially changed thereby and having a melting point materially above the boiling point of liquid oxygen, heating said collected liquid oxygen without substantially changingthe attendant temperature and pressure during the entire distillation whereby a gas phase is evolved while the vapor pressure of said impurity re- .mains negligible, separating the gas phase from 2.
- the process of removing inflammable im- I purities from oxygen during the commercial production of liquid oxygen which process com- -prises collecting oxygen substantially 'in the liquid phase and containing the undesired impurity, said impurity occurring in the collected liquid oxygen at a concentration such that the boiling point of the liquid oxygen is not substantially changed thereby and having a melting point materially above the boiling point of liquid oxgen, heating said collected liquid oxygen without substantially changing the attendant temperature and pressure during the entire distillation whereby a gas phase is evolved while the vapor pressure of said impurity remains negligible, separating the gas phase from the liquid phase while maintaining the vapor pressure of said impurity at a substantially negligible value whereby said impurity remains wholly in the liquid phase, collecting and condensing the separated gas in a region at a lower temperature than that to which the collected liquid oxygen is heated, and thereafter withdrawing substantially all of the condensate.
- the process of removing inflammable impurities from oxygen during the commercial production of liquid oxygen comprises collecting' oxygen substantially in the liquid phase andcontai'ning the undesired impurity, said impurity occurring in the collected liquid oxygen at a concentration such that the boiling point of the liquid oxygen is not substantially changed thereby and having a melting point materially above the boiling point of liquid oxygen, causing evaporation of said liquid oxygenvto take place in a heat exchanger without substantially changing the attendant temperature and pressure during the entire distillation whereby liquid and gas phases coexist therein, refluxing the gas phase with condensate, leading off the washed vapors at a point where the vapor pressure of said impurity is negligible, collecting and condensing said ledoif washed vapors at a temperature lower than the liquid oxygen being evaporated, and withdrawing substantially all of the condensate without interference from reflux material.
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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
July 24, 1934. w E MOELLER 1,967,717
PROCESS FOR PURIFYING LIQUEFIED GASES Filed April 25, 1932 2 Sheets-Sheet 1 1, EH 19 1s g/jj i INVENT OR mm? mm, EMMU W y 24, 1934- w. F. MOELLER 1,967,717
PROCESS FOR PURIFYING LIQUEFIED GASES Filed April 23, 1952 2 Sheets-Sheet 2 INVENTOR Patented July 24, 1934 UNITED STA 1,967,717 PROCESS FOR PURIFYING LIQUEFIED GASES Walter F. Moeller, Buflalo,
assignments, to The Company, New York, N. Y.,
mesne Ohio N. Y., assignor, by. Linde Air Products a corporation of Application April 23, 1932, Serial No. 607,032
4Claims.
This invention relates to a process and apparatus for purifying liquefied gases, particularly liquefied gases having low boiling points, such as liquid oxygen, nitrogen, and the like,
5 which are produced in a manufacturing cycle,-
where they are generally contaminated with undesirable impurities and has for its main object an improved procedure whereby such impurities are readily and expeditiously removed.
More specifically, the invention relates to the provision of suitable steps for concentrating undesired impurities occurring -in the production of liquefied gases of the character indicated in a manner in the cycle. of production such that the impurities may be separated readily by mechanical means, whereby a gas product is finally obtained in the liquid phase from which substantially all I impurities are practically completely removed.
Another object is to produce a liquefied gas in a purified condition with an expenditure of a relatively small amount of additional energy and at relatively little additional cost.
Still another object is to separate the desired liquefied gas from the undesired impurity by the step either of partial evaporation or partial condensation and thereafter causing the gas material to revert to the liquid phase with an expenditure of a relatively small amount of energy.
Other objects of the invention will in part be obvious and will in part appear hereinafter.
Ifhe invention accordingly comprises the several steps and the relation of one or more of such steps with respect to each of the others,
and the apparatus embodying features of construction, combinations of elements and arrangement of parts which are adapted to eflect such steps, all as exemplified in the following detailed disclosure, and the scope of the appli-- cation of which will be indicated in the claims.
For afuller understanding of the nature and objects of the invention reference should be had to the following detailed description taken in connection with the accompanying drawings,
in which:
Fig. i is a view mainly in vertical cross section showing a simple form of apparatus adapted for carrying out the process of the present invention; and
Fig. 2. is a view mainly in vertical section showing a gas production apparatus incorporating purifying apparatus arranged for the prac tice of the present invention.
In the production of a purified liquefied gas from which undesirable impurities are substantially completely removed, the purification may be accomplished with the expenditure o1 relatively little energy by taking the gas material in the liquid phase and treating it by the step of partial evaporation to produce two phases and then separating the phases. Such a process is generically set forth in the copending application filed in the name of Lawrence J. Bowditch on April 23, 1932, Serial No. 607,074, where 6 it is proposed to remove those impurities which occur in relatively small amounts in liquefied gases such as liquid air, oxygen, and the like, the concentration they do not materi carbon dioxide, being such that ally change the boiling point of the liquefied gas, but are otherwise objectionable and impair the commercial qualities of the gas product.
There are certain types of impurities commonly incorporated with the gas material, on account of the source from whichthe gas is obtained and on account of the manufacturing steps commonly employed, which are less volatile than the gas material, i. e. have melting perature and pressure where the vapor of the impurity is pressure of a negligible value. Two
phases are thus produced that may be separated physically while the impurities remain in the liquid or solid phase.
Here it is proposed to conjunction with a finally to obtain a practice these steps in step of condensation, in order liquefied gas such as liquid oxygen in substantially pure condition, this step being preferably practiced so as to the condensation by product from another production.
Referring now larly to Fig. l, A denotes generally accomplish the utilization of a byportion of the cycle of to the drawings, and particue a part of the apparatus into which the gas material in liquid phase that is to be purified is passed and caused to evaporate partially by the application of heat,
while B denotes a second part located at such a distance from part 'A that the vapor pressure of the high boiling is negligible serving ducedin part A, and recondensed contact with a fiui point impurity or impurities to condesnse the vapor prowhich is conducted thereto by bringing it into thermal d of lower temperature than 0 the condensing temperature of the gas material being purified.
The vaporizing portion of part A consists of a vessel 10 having an inlet conduit 11 for the liquefied gas, an outlet conduit 12 for the vapor, and a drain conduit 13 with a control valve 13 In the lower part of vessel 10 is a. suitable heating means, for example a coil 14 provided with inlet and outlet connections adapted to be supplied with a heating agent. This agent may be any convenient vehicle that will pass without difficulty at thelow operating temperatures here employed, for example, compressed air. In the preferred form of the apparatus, the vapor outlet. conduit 12 surrounds the inlet conduit 11 in order to effect heat exchange and separation of the liquid from the gas phase; the vapor thus separated being led from the top of the evaporating vessel 10 over refluxing means to the condenser.
The condenser shown in connection with part B consists of an upper header 15 and a lower header 16 connected by condenser tubes 17. The conduit 12 is here shown as discharging the vapor to be condensed into the upper header 15, while a conduit 18 is connected to the lower header to withdraw the reliquefied gas. The condenser is disposed within a chamber 19 having inlet and outlet conduits 20 and 21, respectively, for the purpose of circulating a cooling medium, for example, liquefied oxygen, or a cold gaseous material that may be a by-prodnot drawn from another part of the manufacturing cycle; the cooling medium carrying away the heat from the condenser so that re-liquefaction is readily accomplished in the condenser.
The operation of the process in the apparatus described is as follows: In previous portions of the manufacturing cycle, certain impurities are not entirely removed and hence appear though in relatively small quantities in the liquefied gas which enters the vaporizer A through conduit 11. The flow of liquid into the vaporizer and the rate at which heat is supplied by the heating fluid passing through the coil 14 are adjusted by the operator to maintain a certain liquid level in the evaporator. The supply of heat causes evaporation of the liquid to occur, but the impurities, which are solid or in solution have a negligible vapor pressure at the temperature of the evaporating liquid, and remain in the liquid and are concentrated at this point in the cycle. The concentrated impurities may be drawn off at will through conduit 13 by means of valve 13, together with some of the liquefied gas.
The vapor is conducted through conduit 12 into the condenser at its upper header 15 whence it passes into the tubes 17 and is condensed because it loses heat through the tube walls to the fluid of lower temperature surrounding the tubes. The liquefied gas collects in the lower header 16 from which it is withdrawn through conduit 18 in a punfied state.
In the modified form of apparatus shown in Fig. 2, a heat interchanger for the manufacture of liquefied oxygen is modified and arranged to separate out the impurities which have relatively high boiling points and are in general inflammable, and then recondense the purified oxygen in order to supply it in the liquid phase. Here a conduit 25 provided with an expansion valve 26 is arranged to supply compressed air drawn from a suitable high pressure source to the rectifying column shown generally at 27. This rectifying column is-provided with a K61;-
. mediate portion 43.
tle or evaporator 28 at its lower end anda condenser 29 at its upper end. A conduit 30 provided with an expansion valve 31 and distributor 32 is arranged to draw liquid from the evaporator 28 and to discharge it into the upper portion of a second rectifying column 33 disposed above the column 2'? and arranged to be in heat exchanging relation with the condenser 29. Each of these columns is provided with suitable counter-current contact cooling means, for example, a series of perforated trays, as shown at 2'7 in the column 27 and at 33 in the column 33. The evaporator 28 associated with the column 27 is provided with suitable heating means, for example a heating coil as shown at 28'.
.Within the column 2'7 is a tray 27 arranged to collect the condensate which drips from the condenser 29 and to convey the same to a conduit 34 having a controlling valve 35 and 'a distributor 36 discharging into the top of the column 33, the distributor 36 being preferably disposed above the distributor 32. From the-top of the condenser 29 is a gas withdrawal conduit 37 -which is arranged for withdrawing non-condensible vapors, while a liquid withdrawal conduit 38 is arranged to withdraw liquid from the .base of the column 33 from about the condenser From this arrangement, it is seen that the compressed air introduced into the column 27 is liquefied by the passage through the expansion valve 26 and through the trays 27'; the liquid collecting in the evaporator 28. Gas or vapor rising through the column 2'? passes into the condenser 29 where the less volatile portion is recondensed and produces a reflux in the column 27. Liquid nitrogen collects in the tray 27", whereas the liquid in the evaporator 28 comprises a relatively large percentage 'of liquid oxygen. Any non-condensible vapor that is more volatile than liquid nitrogen or oxygen is withdrawn through the conduit 37. Liquefied gas comprising mainly liquid oxygen and'the impurities of relatively high melting point are withdrawn through the conduit 30 and introduced into the column 33 through the distributor 32.
In order to effect the final stage of purification, in accordance with the present invention, a second condenser shown generally at 40 is incorporated at a point in the column 33 where the vapor pressure of the undesired impurity is negligible. This condenser comprises upper and lower portions 41 and 42, connected by an inter- One or more passages or flues 44 are associated with the condenser in order to establish communication between the space above the condenser with the space below; a chamber for this condenser being preferably provided in the column by means of a partition 45 disposed transversely in the column below the condenser and a second partition 46, which is disposed above the condenser. This chamber occupies a space normally occupied by refluxing means such as counter-current contact cooling trays, and preferably has trays both above and belowthe same, those shown below being -denoted 33".
The partition 46 is provided with one or more passages 47 that permits communication with the flues 44 so as to establish communication in the column 33 for the space on the two sides of the condenser chamber containing condenser 40.. The partition 46 is also provided with one or more liquid drains 48 which allow liquid to drain from the partition into the chamber about the condenser 40. Gaseous oxygen to be recondensed and'which has been evaporated by the condenser 29- is led from a. point near the lower end of the column 33 from the chamber about the condenser 29 by means of a conduit 50 and passed into the portion 41 of condenser 40. Here liquid oxygen collects in a purified state and is withdrawn from the lower portion 42 through a conduit 51.
The operation of this latter form of apparatus is seen to be as follows: The compressed air from which oxygen in the liquid phase and in a purified state is desired to be obtained is introduced into the rectifying column 27 either with or without previous partial purification. This is then passed through the conduit 30, the=expansion valve 31 and the distributor 32 into the column 33, where the cooled oxygen condenses out and passes down through the trays 33' and through the drain 48 into the chamber about the condenser 40. When the desired liquids'level is attained in this chamber, the cooled liquid overflows through the by-pass 44 into the lower portion of the column 33 over the trays 33" and finally collects in the chamber about the condenser 29. Here the heat absorbed from the condenser 29 in effecting refrigeration for the column 2'7 vaporizes a portion of the liquid which is now a high concentrate of liquid oxygen contaminated with the impurities of relatively high melting point. The oxygen vaporized in this chamber is substantially pure oxygen gas which is *withdrawn through the conduit 50 and passed into the condenser 40, where it is recondensed bythe heatabstracted by the liquid in the chamber about the condenser 40. Thus it is seen.
that liquefied oxygen in the purified state desired collects in the portion 42. and is withdrawn by the conduit 51.
The liquid which collects in the chamber about the condenser 40 is seen to comprise a mixture of oxygen and nitrogen in the liquid phases, together with any substances that may be present either as solids or in solution. The vaporization which takes place in this chamber is of a fractional nature, the more volatile nitrogen being boiled oif and passed up through the fiues 47 into the upper portion of the column 33. This liquid nitrogen is seen to be supplied to the column mainly from the conduit 34; thus the cooling of the condenser 40 is seen to be accomplished by means of a cooling agent that is withdrawn from another portion of the cycle of production. The vaporized nitrogen is seen to pass from the top of the column 33 in the usual manner.
The agents here used for heating the liquid in the evaporators and for extracting heat from the vapor in the condensers, in order to con; serve energy, are thus with advantage both taken from some other portions of the cycle of production, and since no change has occurred therein otherthan a change in the quantity of absorbed heat, they may be returned, if desired, to the cycle substantially without loss.
Since certain changes in carrying out the above process and in the constructions set forth,
which embody the invention may be made without departing from its scope, it is intended that all matterxcontained in the above description as new and desire to secure by Letters Patent, is:
1. The process of removing inflammable impurities from oxygen during the commercial production of liquid oxygen, which process comprises collecting oxygen substantially in the liquid'phase and containing the undesired impurity, said impurity occurring in the collected liquid oxygen at a concentration such that the boiling point of the liquid oxygen is not substantially changed thereby and having a melting point materially above the boiling point of liquid oxygen, heating said collected liquid oxygen without substantially changingthe attendant temperature and pressure during the entire distillation whereby a gas phase is evolved while the vapor pressure of said impurity re- .mains negligible, separating the gas phase from 2. The process of removing inflammable im- I purities from oxygen during the commercial production of liquid oxygen, which process com- -prises collecting oxygen substantially 'in the liquid phase and containing the undesired impurity, said impurity occurring in the collected liquid oxygen at a concentration such that the boiling point of the liquid oxygen is not substantially changed thereby and having a melting point materially above the boiling point of liquid oxgen, heating said collected liquid oxygen without substantially changing the attendant temperature and pressure during the entire distillation whereby a gas phase is evolved while the vapor pressure of said impurity remains negligible, separating the gas phase from the liquid phase while maintaining the vapor pressure of said impurity at a substantially negligible value whereby said impurity remains wholly in the liquid phase, collecting and condensing the separated gas in a region at a lower temperature than that to which the collected liquid oxygen is heated, and thereafter withdrawing substantially all of the condensate.
3. The process of removing inflammable impurities from oxygen during the commercial production of liquid oxygen, which process comprises collecting' oxygen substantially in the liquid phase andcontai'ning the undesired impurity, said impurity occurring in the collected liquid oxygen at a concentration such that the boiling point of the liquid oxygen is not substantially changed thereby and having a melting point materially above the boiling point of liquid oxygen, causing evaporation of said liquid oxygenvto take place in a heat exchanger without substantially changing the attendant temperature and pressure during the entire distillation whereby liquid and gas phases coexist therein, refluxing the gas phase with condensate, leading off the washed vapors at a point where the vapor pressure of said impurity is negligible, collecting and condensing said ledoif washed vapors at a temperature lower than the liquid oxygen being evaporated, and withdrawing substantially all of the condensate without interference from reflux material.
4. The process of removing impurities from oxygen which occur in small amounts therein when obtained from the atmosphere in the commercial production of liquid oxygen, which process comprises collecting oxygen substantially in, the liquid phase and containing the undesired impurity, said impurity occurring in said liquid oxygen at a concentration such, that the boiling point of the liquid oxygen is not substantially changed thereby and having a melting point materially above the boiling point of liquid oxygen, bringing said liquid oxygen containing said impurity in a heat exchanger to a temperature and pressure corresponding substantially to a point of the liquid-gas phase equilibrium curve where it remains during substantially the entire distillation while at the same time reducing the vapor pressure of said impurity to a substantially negligible value, adding heat to the introduced oxygen in a manner such that
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR754118D FR754118A (en) | 1932-04-23 | ||
| US607032A US1967717A (en) | 1932-04-23 | 1932-04-23 | Process for purifying liquefied gases |
| GB6554/33A GB416051A (en) | 1932-04-23 | 1933-03-03 | Improvements in or relating to processes of and apparatus for purifying liquefied gases |
| US672191A US1967718A (en) | 1932-04-23 | 1933-05-22 | Apparatus for purifying liquefied gases |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US607032A US1967717A (en) | 1932-04-23 | 1932-04-23 | Process for purifying liquefied gases |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1967717A true US1967717A (en) | 1934-07-24 |
Family
ID=24430518
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US607032A Expired - Lifetime US1967717A (en) | 1932-04-23 | 1932-04-23 | Process for purifying liquefied gases |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1967717A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2807574A (en) * | 1953-10-21 | 1957-09-24 | Hirano Masao | Treatment of unreacted ammonia in the manufacture of urea |
-
1932
- 1932-04-23 US US607032A patent/US1967717A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2807574A (en) * | 1953-10-21 | 1957-09-24 | Hirano Masao | Treatment of unreacted ammonia in the manufacture of urea |
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