AU631578B2 - Air separation - Google Patents

Air separation Download PDF

Info

Publication number
AU631578B2
AU631578B2 AU45546/89A AU4554689A AU631578B2 AU 631578 B2 AU631578 B2 AU 631578B2 AU 45546/89 A AU45546/89 A AU 45546/89A AU 4554689 A AU4554689 A AU 4554689A AU 631578 B2 AU631578 B2 AU 631578B2
Authority
AU
Australia
Prior art keywords
column
stream
liquid
oxygen
fraction
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
AU45546/89A
Other versions
AU4554689A (en
Inventor
Martin Peter Eaglen
John Douglas Oakey
Robert Owen
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BOC Group Ltd
Original Assignee
BOC Group Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by BOC Group Ltd filed Critical BOC Group Ltd
Publication of AU4554689A publication Critical patent/AU4554689A/en
Application granted granted Critical
Publication of AU631578B2 publication Critical patent/AU631578B2/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F25REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
    • F25JLIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
    • F25J3/00Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification
    • F25J3/02Processes 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
    • F25J3/04Processes 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
    • F25J3/04763Start-up or control of the process; Details of the apparatus used
    • F25J3/04866Construction and layout of air fractionation equipments, e.g. valves, machines
    • F25J3/04969Retrofitting or revamping of an existing air fractionation unit
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F25REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
    • F25JLIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
    • F25J3/00Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification
    • F25J3/02Processes 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
    • F25J3/04Processes 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
    • F25J3/04436Processes 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 at least a triple pressure main column system
    • F25J3/04454Processes 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 at least a triple pressure main column system a main column system not otherwise provided, e.g. serially coupling of columns or more than three pressure levels
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F25REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
    • F25JLIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
    • F25J3/00Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification
    • F25J3/02Processes 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
    • F25J3/04Processes 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
    • F25J3/04642Recovering noble gases from air
    • F25J3/04648Recovering noble gases from air argon
    • F25J3/04654Producing crude argon in a crude argon column
    • F25J3/04709Producing crude argon in a crude argon column as an auxiliary column system in at least a dual pressure main column system
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F25REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
    • F25JLIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
    • F25J2200/00Processes or apparatus using separation by rectification
    • F25J2200/34Processes or apparatus using separation by rectification using a side column fed by a stream from the low pressure column
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F25REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
    • F25JLIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
    • F25J2215/00Processes characterised by the type or other details of the product stream
    • F25J2215/50Oxygen or special cases, e.g. isotope-mixtures or low purity O2
    • F25J2215/56Ultra high purity oxygen, i.e. generally more than 99,9% O2
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F25REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
    • F25JLIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
    • F25J2220/00Processes or apparatus involving steps for the removal of impurities
    • F25J2220/50Separating low boiling, i.e. more volatile components from oxygen, e.g. N2, Ar
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F25REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
    • F25JLIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
    • F25J2220/00Processes or apparatus involving steps for the removal of impurities
    • F25J2220/52Separating high boiling, i.e. less volatile components from oxygen, e.g. Kr, Xe, Hydrocarbons, Nitrous oxides, O3
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F25REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
    • F25JLIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
    • F25J2235/00Processes or apparatus involving steps for increasing the pressure or for conveying of liquid process streams
    • F25J2235/50Processes or apparatus involving steps for increasing the pressure or for conveying of liquid process streams the fluid being oxygen
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F25REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
    • F25JLIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
    • F25J2245/00Processes or apparatus involving steps for recycling of process streams
    • F25J2245/02Recycle of a stream in general, e.g. a by-pass stream
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F25REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
    • F25JLIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
    • F25J2245/00Processes or apparatus involving steps for recycling of process streams
    • F25J2245/58Processes or apparatus involving steps for recycling of process streams the recycled stream being argon or crude argon

Landscapes

  • 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

3157 COMMONWEALTH OF AUSTRALIA FORM PATENTS ACT 1952 SC M P T. T R PFC r T FT r AT T FOR OFFICE USE: Class Int.Class Application Number: Lodged: Complete Specification Lodged: Accepted: Published: SPriority: Related Art: Name of Applicant: Address of Applicant: Actual Inventor: Actual Inventor: THE BOC GROUP plc Chertsey Road, Windlesham, Surrey 6HJ, England Martin Peter Eaglen, Robert Owen and John Douglas Oakey Address for Service: SHELSTON WATERS, 55 Clarence Street, Sydney t SComplete Specification for the Invention entitled: "AIR SEPARATION" The following statement is a full description of this invention, including the best method of performing it known to us:- 1
C
la- AIR SEPARATION This invention relates to air separation. In particular, it relates to the production of what is sometimes termed "ultra high purity" or "ultra pure" oxygen.
Many tens of thousands of tons of high purity oxygen are produced per year worldwide. The oxygen is produced by the well-known process of fractionally distilling air at cryogenic temperatures. The oxygen produced typically has a purity in the range of 99.5 99.9%. This purity makes it suitable for use in a large number of industrial processes.
The main impurity in the high purity oxygen is argon. However, there is typically in the order of 10 volumes per million (vpm) of methane. The presence of methane, in particular, may be undesirable in a few processes, for example, th& fabrication of micro-electronic products. Accordingly, there is a demand for oxygen of a higher purity than that normally provided.
One way of meeting the demand is to subject the oxygen to a process of catalytic combustion so as to remove traces of m'thane. However, in some instances, this process is not suitable because the gas becomes contaminated with parti6les generated from the catalyst granules. Alternative purification methods are known. These generally involve subjecting the normal high purity oxygen to two further cryogenic separation stages, the first involving removal of heavy impurities, such as methane, having a vapour pressure less than oxygen, and the second the removal of light impurities having a vapour pressure greater than oxygen. See, for example, US patent specifications 3 363 427 and 4 755 202.
The process described in US patent 4 755 202 produces from the column removing light impurities a first gaseous product comprising ultra high purity oxygen having a minimum of impurities and second an oxygen product having a level of impurities which makes it acceptable as normal high purity oxygen. This second oxygen product does, however, contain a significant proportion of argon which is itself a valuable commercial product. The r 2 invention relates to a process in which at least some of the argon can be recovered.
According to the present invention there is provided a process for producing ultra pure oxygen from a gaseous feed containing oxygen, light impurities and heavy impurities, said gaseous feed having been withdrawn from the lower pressure column of a conventional double-column air separation arrangement, said process comprising the steps of: introducing the gaseous feed into a first liquid-vapour contact column, absorbing heavy impurities into descending liquid, and thereby producing a first fraction having an enhanced concentration of heavy impurities and a second fraction having a reduced concentration of heavy impurities; condensing a first gaseous stream of said second fraction and supplying resulting condensate to the first column as reflux; withdrawing a second stream of said second fraction from the first column and introducing it into a second liquid-vapour contact column in which light impurities are stripped from descending liquid by ascending vapour, said second column being provided with a reboiler, wherein: SALI the second stream is introduced into U the second column at a level above which there are liquid-vapour contact
NA
3 surfaces for the fractionation for the gas whereby there is produced at the top of the column a fraction having a substantially greater concentration of light impurities than the incoming feed; (ii) condensing a portion of the fraction enriched light impurities and returning thus formed condensate to the second column as reflux; and returning a stream of the fraction enriched in light impurities to further fractionation in said lower pressure column of said double-column arrangement, wherein said lower pressure column is fitted with a 'side 15 column' which receives an argon-enriched feed from the lower pressure column and fractionates that feed to produce a crude argon product and an argon depleted fluid that is returned to the lower pressure column.
The invention also provides apparatus for performing this process.
Preferably, the stream taken for further fractionation contains at least 5% by volume of argon.
Preferably, the said second stream is introduced into the said second column as a gas or vapour and not a liquid. This helps to reduce the amount of refrigeration required for the condenser associated with the first L column.
-C I I 3a Preferably, when the oxygen feed is produced by fractionation of air in a conventional double column, the condenser associated with the said first column is refrigerated by a part of the oxygen-poor liquid withdrawn from the higher pressure column of the double column arrangement. We have found that in any conventional double column arrangement, the top of the lower pressure column is typically provided with excessive reflux. This reflux is normally provided by the PL. By taking a portion of the PL to provide condensation for the said first column, a more suitable rate of supplying reflux to the lower pressure column can be attained.
Preferably, heat for the reboiler associated with the said second column and cooling for the condenser associated with the said second column can be provided by a heat pump circuit in which the working fluid is air.
The process and apparatus according to the 00 invention will now be described by way of example with o 20 reference to the accompanying drawings which is a schematic circuit diagram illustrating an air separation 000 plant.
-4- Referring to the drawing, there is shown an arrangement of columns separating air into oxygen, nitrogen and argon products and for producing and ultra pure oxygen product typically containing less than tell volumes per million of impurities. Incoming air feed typically at its dew point is subjected to distillation in a double column 2 comprising a higher pressure column 4 and a lower pressure column 6. The double column 2 provides oxygen and nitrogen products and a feed of argon-enriched oxygen to a side column 8 in which the argon-enriched oxygen is subjected to further separation to produce a crude argon product. The arrangement of columns shown in the drawing also includes a first purification column 10 for purifying gaseous oxygen produced by the double column 2 and a second purification column 12 S which provides further purification and produces an ultra high purity oxygen product typically containing less than 1 volume per million of impurities.
The double column 2 and the side col.umn 8 and their operation are generally conventional (save for the return of a stream from the column 12 to the column 6 which will be described herein below). It will be appreciated that the heat exchangers that are normally employed in association with the columns 2 and 8 are omitted from the drawing for purposes of ease of illustration. For one typical arrangement of such heat exchangers and for a description of the operation of a double column, with a side column for producing crude argon, attention is directed to Figure 1 of European patent application 296 342 A and the description thereof. Since this invention is primarily concerned with the purification of the oxygen product from the double column 2, only an abbreviated description will be given herein of its operation and of the operation of the column 8.
Air is introduced into the higher pressure column 4 through-an inlet 14. It is separated into oxygen-enriched liquid and oxygen-poor liquid The column 4 is provided with a condenser 20 at its top which provides liquid nitrogen reflux for it and which also provides reboil for the lower pressure column 6. A stream of oxygen-rich liquid is withdrawn from the bottom of the column 4 through an outlet 16 and after subcooling (by means not shown) is introduced into the lower pressure column 6 through an inlet 22. The fluid that is thus introduced into the column 6 is separated into oxygen and nitrogen fractions. To provide liquid nitrogen F-
_I
reflux for the lower pressure column 6 a stream of PL is withdrawn from the higher pressure column 4, is subcooled (by means not shown) and is then divided into two sub-streams, one of which is passed through a Joule Thomson valve 24 and then through an inlet 26 leading into the top of the lover pressure column 6.
If desired, air may be introduced directly into the lower pressure column 6 through an inlet 28. This air is known as "Lachmann air" and its use is well known in the art. Oxygen and nitrogen fractions are produced, both typically of a purity between 99.0 and 99.9%. A gaseous nitrogen product is withdrawn from the top of the column 6 through an outlet 30 and a gaseous oxygen product from the bottom of the column 6 through an outlet 32. In addition, the waste nitrogen stream is withdrawn from the column 6 through an outlet 34 (and is used for the purposes of regenerating a reversing heat exchanger or other purification unit for removing water vapour and carbon dioxide from the air feed). An argon-enriched oxygen vapour stream is withdrawn from the column 6 through an outlet 36 and is introduced into the column 8 which is provided with a condenser 38 and which separates the argon-enriched oxygen into a crude argon fraction which collects at the top of the column 8 and is typically withdrawn in liquid state through the outlet 40. In addition, a liquid oxygen stream is returned from the bottom of the column 8 through the outlet 42 to the column 6.
444 As well as producing a gaseous oxygen product, the double column 2 may if S desired be used to produce a liquid oxygen product and a stream of liquid oxygen may be withdrawn from the column 6 through an outlet 44 and then 14464 oo 25 pumped to storage by means of pumps 46 and 48.
A part of the gaseous oxygen product produced by the column 2 is introduced as a stream into the first purification column 10 at its bottom. In this column heavy impurities, particularly methane, are stripped from the gaseous oxygen by being adsorbed into the liquid phase. Accordingly, as the vapour ascends the column 10 so it becomes leaner in heavy impurities until at the top of the column it is essentially free of them. A stream of vapour is withdrawn from the top of the column 10 through the outlet 52 and a part of it is condensed in a condenser 54 and is returned to the top of the column -6through the inlet 56. As the liquid descends the column 10 so it becomes progressively richer in heavy impurities. A liquid oxygen fraction containing essentially all the heavy impurities thus collects at the bottom of the column 10 and a stream of such liquid oxygen is withdrawn through the outlet 58. Since typically the oxygen feed to the column 10 will include in the order of 10 volumes per million of methane, it will be appreciated that the liquid oxygen withdrawn through the outlet 58 will still be of an acceptable purity for use in most commercial applications and accordingly it is united with the liquid oxygen product withdrawn from the column 2 through L °1.0 the outlet 44.
ootO Refrigeration for the condenser 54 is provided by a stream of the PL from o the column 4. This stream is vaporised as it passes through the condenser S 54 and the resulting nitrogen vapour leaves the condenser 54 through an outlet 60 and is typically united with the gaseous nitrogen withdrawn from the column 2 through the outlet Not all the oxygen essentially free of heavy impurities withdrawn from the column 10 through the outlet 52 is condensed in the condenser 54. A stream of uncondensed oxy-en free of heavy impurities is withdrawn from the condenser 54 (or may by-pass the condenser 54 altogether) and is introduzed into the second purification column 12 through an inlet 62 located at an intermediate level thereof. The column 12 is operated so as to separate the oxygen into a fraction that is essentially free of low boiling point impurities (and is thus capable of forming an ultra-high purity oxygen product) and a fraction which is enriched more than ten-fold in argon compared with the argon content of the oxygen entering the column 12 through the inlet 62. The column 12 is thus provided with a reboiler 64 and a condenser 66. The reboiler 64 provides an upward flow of vapour through the column and the condenser 66 provides a downward flow of liquid. Accordingly the vapour becomes progressively richer in light impurities (argon) as it ascends the column 12 and the liquid becomes progressively leaner in light impurities (argon) as it descends the column 12. A liquid oxygen fraction essentially free of both light and heavy impurities (iec. containing no more than 1 vpm of impurities) collects at the bottom of the column 12. A stream of this ultra high purity oxygen is withdrawn from the bottom of the column -7- 12 through an outlet 68 and passed through the reboiler 64 in which it is partially reboiled. The vapour thus formed is returned to column 12 through an inlet 70 while the residual liquid is passed through pipe 72 to storage (not shown).
In addition to the withdrawal of liquid through the outlet 68, a stream of vapour enriched in argon is withdrawn from the top of the column 12 through an outlet 74. This stream is then passed into the condenser 66 in which it is partially condensed. The condensate is returned to the top of the column 12 through an inlet 76 while the uncondensed vapour is returned to the lower pressure column 6 through an inlet 80. Since typically the fraction collecting at the top of the column contains at least 5% by volume of argon, this recycling of the vapour from the column 12 to the column 6 enhances the total yield of argon from the process. Since also the temperature of this stream tends to be lover than the average temperature in the column 6, cold is also recovered. Typically, inlet 80 is situated at the same level as the inlet 28 for Lachmann air.
Heating for the reboiler 64 and cooling for the condenser 66 are preferably provided by means of a heat pump cycle that uses air as the working fluid.
The air is typically taken from the stream that is fed to the column 4 and is introduced into the reboiler 64 at a temperature of 102 K under pressure of approximately 6.5 bar absolute. The air is fully condensed in the condenser 64 and is then flashed through a Joule-Thomson valve 82 so as to reduce its temperature. This reduced temperature condensate then flows through the condenser 66 so as to provide at least part of the cooling for that condenser. If further condenser duty is required, this may be provided by passing a further stream of PL from the column 4 through'the condenser 66. The nitrogen (now gaseous) exiting the condenser 66 may be united with the gaseous nitrogen product withdrawn from the column 6 through the outlet while the air leaving the condenser 66 may be warmed in the main heat exchanger(s) (not shown) of the plant and vented to the atmosphere.
It will be appreciated that the columns 4, 6, 8, 10 and 12 will all contain means for producing intimate contact between ascending vapour and descending liquid. Typically, such means are provided by sieve trays although other 8 -8contacting apparatus such as a packing may be used. In the process according to the invention, the first purification column 10 typically has from 6 to 10 theoretical trays and operates at a reflux or L/V ratio of about 0.5 while the second purification column 12 includes from 60 to theoretical trays operating at a reflux ratio of approximately 60. The inlet 62 is positioned at a level 21 trays from the top of the column.
Further, in this example about one third of the vapour withdrawn from the column 10 through the outlet 52 is returned to the column as reflux while the remaining two thirds are condensed and introduced into the column 12 as feed.
If desired, the columns 10 and 12 and associated condensers and reboiler can be retro-fitted to an existing air separation plant including the columns 4, 6 and 8.
In order to control operation of the first purification column 10, two main controls may be employed. The first control adjusts the flow of PL to the condenser 54 by adjusting the setting of the flow-control valve 86. The setting of the valve is controlled by sensing the pressure drop encountered by the rising vapour in the column 10 which is monitored by a pressure sensor 88. The arrangement allows for a constant pressure drop to be maintained and therefore for the oxygen free of heavy impurities to be withdrawn from the column 10 at a constant rate equal to the required design rate.
The purity of the stream withdrawn through the outlet 52 is maintained indirectly. An analyser-cum-controller analyses the hydrocarbon content of the vapour apart way up the column 10. This analyser 90 biases as valve controller 92 so as to control the setting of a flow control valve 94 in a conduit through which the gaseous oxygen free of heavy impurities flows on its way to the inlet 62 to the column 16. Adjustment of the position of the valve 94 will adjust the exact proportion of the fluid entering the condenser 54 that is retur! to the column 10 as reflux through the inlet 56. Accordingly, the arrai: of the analyser 90, controller 92 and valve 94 is able to maintai. 4 sensed hydrocarbon concentration in the vapour at a chosen level s 'iat the level of hydrocarbon impurity in the 9 gas withdrawn through the outlet 52 of the column 10 does not exceed a chosen level.
Two main controls are also used for the column 12. First, an analyser-cum-controller 96 analyses the argon concentration in the oxygen leaving the top of the column 12 through the outlet 74 and adjusts the setting of a flow control valve 98 in the conduit returning the argon-enriched oxygen to the column 6 near the inlet 80. This accordingly adjusts the amount of vapour to be condensed and hence the reflux rate.
o 8 Accordingly, any fluctuation in the purity at the top of the column 74 can SA0 be corrected. The control of the flow rate of the ultra high purity oxygen 0 withdrawn through the outlet 68 of the column 12 is effected by means of a controller 100 which by adjusting a flow control valve 102 in the ultra high o o purity oxygen outlet pipeline 72 enables a constant head of liquid to be 'oo maintained in the reboiler 64 so that there is a constant product withdrawal rate.
We have performed a computer simulation of the operation of the plant shown SB,, in the drawing and have obtained the results set out in Table 1 below.
10 TABLE 1 Column 10 Column 12 Feed to Top Bottom Recycled Ultra High Inlet 14 Outlet 52 Outlet 58 Ar-enriched purity 02 02 product Flowrate as of feed to 100 67 33 2 64 inlet 14 Temperature 95.5 94.6 95.5 94 96 Pressure [Bara] 1.61 1.54 1.61 1.45 1.6 (min) head) Physical state VAP VAP LIQ VAP LIQ Impurities: Methane 10vpm 5ppb 55vpm Oppb 6ppb Argon 0.3% 0.3% 0.3% 8% 100ppb Krypton 7vpm Oppb 25vpm Oppb Oppb KEY: ppb volumes per billion (thousand million) vkm volumes per million

Claims (6)

1. A process for producing ultra pure oxygen from a gaseous feed containing oxygen, light impurities and heavy impurities, said gaseous gaseous feed having been withdrawn from the lower pressure column of a conventional double-column air separation arrangement, said process comprising the steps of: introducing the gaseous feed into a first liquid-vapour contact column, absorbing heavy impurities into descending liquid, and thereby producing a first fraction having an enhanced concentration of heavy impurities and a second fraction having a reduced concentration of heavy impurities; condensing a first gaseous stream of said second fraction and supplying resulting condensate to the first column as reflux; withdrawing a second stream of said second fraction from the first column and introducing it into a second liquid-vapour contact column in which light impurities are stripped from descending liquid by ascending vapour, said second column being provided with a reboiler, wherein: the second stream is introduced into the second column at a level above which there are liquid-vapour contact b ~surfaces for the fractionation for the U gas whereby there is produced at the 0 12 top of the column a fraction having a substantially greater concentration of light impurities than the incoming feed; (ii) condensing a portion of the fraction enriched light impurities and returning thus formed condensate to the second column as reflux; and returning a stream of the fraction enriched in light impurities to further fractionation in said lower pressure column of said double-column arrangement, wherein said lower pressure column is fitted with a 'side column' which receives an argon-enriched feed from the lower pressure column and fractionates that feed to produce a crude argon product and an argon depleted fluid that is returned to the lower pressure column.
2. A process according to claim 1, in which the condenser associated with said first column is refrigerated by a part of the oxygen-poor liquid withdrawn from said higher pressure column.
3. A process according to any one of the preceding claims, in which the stream taken for further fractionation contains at least 5% by volume of argon.
4. A process according to any one of the preceding claims, in which the said second stream is introduced into the said second column as a gas or vapour and not a liquid.
A process according to any one of the preceding 1 claims, in 13 which heat for the reboiler associated with the said second column and cooling for the condensation associated with the said second column can be provided by a heat pump circuit in which the working fluid is air.
6. A process for producing ultra pure oxygen substantially as herein described with reference to the accompanying drawings. DATED this 3rd day of September, 1992 THE BOC GROUP plc Attorney: LEON K. ALLEN Fellow Institute of Patent Attorneys of Australia of SHELSTON WATERS
AU45546/89A 1988-12-02 1989-11-24 Air separation Ceased AU631578B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB888828134A GB8828134D0 (en) 1988-12-02 1988-12-02 Air separation
GB8828134 1988-12-02

Publications (2)

Publication Number Publication Date
AU4554689A AU4554689A (en) 1990-06-07
AU631578B2 true AU631578B2 (en) 1992-12-03

Family

ID=10647838

Family Applications (1)

Application Number Title Priority Date Filing Date
AU45546/89A Ceased AU631578B2 (en) 1988-12-02 1989-11-24 Air separation

Country Status (7)

Country Link
EP (1) EP0376464A1 (en)
JP (1) JPH02223786A (en)
AU (1) AU631578B2 (en)
CA (1) CA2004368A1 (en)
DK (1) DK607789A (en)
GB (1) GB8828134D0 (en)
ZA (1) ZA899075B (en)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2693220B2 (en) * 1989-04-24 1997-12-24 テイサン株式会社 Ultra high purity oxygen production method
JP2966999B2 (en) 1992-04-13 1999-10-25 日本エア・リキード株式会社 Ultra high purity nitrogen / oxygen production equipment
EP0570648A1 (en) * 1992-05-21 1993-11-24 International Business Machines Corporation Apparatus for generating and checking the error correction codes of messages in a message switching system
US5425241A (en) * 1994-05-10 1995-06-20 Air Products And Chemicals, Inc. Process for the cryogenic distillation of an air feed to produce an ultra-high purity oxygen product
US5528906A (en) * 1995-06-26 1996-06-25 The Boc Group, Inc. Method and apparatus for producing ultra-high purity oxygen
US5546767A (en) * 1995-09-29 1996-08-20 Praxair Technology, Inc. Cryogenic rectification system for producing dual purity oxygen
EP0793069A1 (en) * 1996-03-01 1997-09-03 Air Products And Chemicals, Inc. Dual purity oxygen generator with reboiler compressor
US5628207A (en) * 1996-04-05 1997-05-13 Praxair Technology, Inc. Cryogenic Rectification system for producing lower purity gaseous oxygen and high purity oxygen
JP6427359B2 (en) * 2014-08-12 2018-11-21 神鋼エア・ウォーター・クライオプラント株式会社 Method and apparatus for producing ultra-high purity oxygen

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3363427A (en) * 1964-06-02 1968-01-16 Air Reduction Production of ultrahigh purity oxygen with removal of hydrocarbon impurities

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SU757817A1 (en) * 1977-01-11 1980-08-23 Le T I Kholodilnoi Prom Method of producing high-purity oxygen
US4867772A (en) * 1988-11-29 1989-09-19 Liquid Air Engineering Corporation Cryogenic gas purification process and apparatus

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3363427A (en) * 1964-06-02 1968-01-16 Air Reduction Production of ultrahigh purity oxygen with removal of hydrocarbon impurities

Also Published As

Publication number Publication date
EP0376464A1 (en) 1990-07-04
CA2004368A1 (en) 1990-06-02
JPH02223786A (en) 1990-09-06
GB8828134D0 (en) 1989-01-05
AU4554689A (en) 1990-06-07
DK607789D0 (en) 1989-12-01
ZA899075B (en) 1990-09-26
DK607789A (en) 1990-06-03

Similar Documents

Publication Publication Date Title
EP0173168B1 (en) Process to produce ultrahigh purity oxygen
EP0577349B1 (en) Air separation
US4934147A (en) Cryogenic gas purification process and apparatus
AU694000B2 (en) Air separation
US5106398A (en) Air separation
AU631578B2 (en) Air separation
US5692398A (en) Production of argon
US5660059A (en) Air separation
JP2776461B2 (en) Air separation method by cryogenic distillation to produce ultra-high purity oxygen
EP0182620B1 (en) Nitrogen generation
US5511380A (en) High purity nitrogen production and installation
CA2083562C (en) Cryogenic rectification system for producing elevated pressure product
JPH07305954A (en) Raw-material air low-temperature distillation method manufacturing extra-high purity oxygen product
US5361590A (en) Air separation
AU643232B2 (en) Cryogenic air separation process and apparatus
AU706679B2 (en) Air separation
US6220054B1 (en) Separation of air
EP0768504A2 (en) Air separation
EP0828124B1 (en) Air separation
AU719240B2 (en) Air separation
US6170291B1 (en) Separation of air
EP0828123B1 (en) Air separation
EP1760415A1 (en) Process and device for the production of argon by cryogenic separation of air
CA2034740C (en) Cryogenic air separation system with hybrid argon column
EP0770840A2 (en) Air separation