[0001] 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.
[0002] 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.
[0003] 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, the fabrication
of micro-electronic products. Accordingly, there is a demand for oxygen of a higher
purity than that normally provided.
[0004] One way of meeting the demand is to subject the oxygen to a process of catalytic
combustion so as to remove traces of methane. However, in some instances, this process
is not suitable because the gas becomes contaminated with particles 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.
[0005] 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 invention relates to a process in which at least some of the argon can be recovered.
[0006] 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,
comprising:
(a) 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;
(b) condensing a first gaseous stream of said second fraction and supplying resulting
condensate to the first column as reflux;
(c) withdrawing a second steam 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, characterised in that:
(i) the second stream is introduced into the second column at a level above which
there are liquid-vapour contact 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 in light impurities and returning
thus formed condensate to the second column as reflux; and
(iii) subjecting a stream of the fraction enriched in light impurities to further
fractionation in at least one column other than said first and second columns and
recovering an argon product therefrom.
[0007] The invention also provides apparatus for performing this process.
[0008] Preferably, the stream for further fractionation to recover the light impurity (argon)
product is returned to the same column from which the gaseous oxgyen feed is taken.
This column is typically the lower pressure column of a conventional double column
arrangement and is fitted with a "side column" which receives an argon-enriched feed
from the lover 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.
[0009] Preferably, the stream taken for further fractionation contains at least 5% by volume
of argon.
[0010] 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 column.
[0011] 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 ("PL") 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.
[0012] 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.
[0013] The process and apparatus according to the invention will now be described by way
of example with reference to the accompanying drawing which is a schematic circuit
diagram illustrating an air separation plant.
[0014] 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 ten 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 which provides further purification
and produces an ultra high purity oxygen product typically containing less than 1
volume per million of impurities.
[0015] The double column 2 and the side column 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.
[0016] Air is introduced into the higher pressure column 4 through an inlet 14. It is separated
into oxygen-enriched liquid ("RL") and oxygen-poor liquid ("PL"). 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 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 lower pressure column 6.
[0017] 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.
[0018] As well as producing a gaseous oxygen product, the double column 2 may if 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 pumped to storage by means of pumps
46 and 48.
[0019] 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 10 through 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 the
outlet 44.
[0020] Refrigeration for the condenser 54 is provided by a stream of the PL from the column
4. This stream is vaporised as it passes through the condenser 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 30.
[0021] 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
oxygen free of heavy impurities is withdrawn from the condenser 54 (or may by-pass
the condenser 54 altogether) and is introduced 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 (ie. 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 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).
[0022] 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 lower 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.
[0023] 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 30, 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.
[0024] 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 contacting 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
80 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.
[0025] 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.
[0026] 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.
[0027] 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 returned to the column 10 as reflux through the inlet 56.
Accordingly, the arrangement of the analyser 90, controller 92 and valve 94 is able
to maintain the sensed hydrocarbon concentration in the vapour at a chosen level such
that the level of hydrocarbon impurity in the gas withdrawn through the outlet 52
of the column 10 does not exceed a chosen level.
[0028] 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. Accordingly,
any fluctuation in the purity at the top of the column 74 can be corrected. The control
of the flow rate of the ultra high purity oxygen 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 purity oxygen outlet pipeline 72 enables a constant head
of liquid to be maintained in the reboiler 64 so that there is a constant product
withdrawal rate.
[0029] We have performed a computer simulation of the operation of the plant shown in the
drawing and have obtained the results set out in Table 1 below.
TABLE 1
|
|
Column 10 |
Column 12 |
|
Feed to Inlet 14 |
Top Outlet 52 |
Bottom Outlet 58 |
Recycled Ar-enriched O₂ |
Ultra High purity O₂ product |
Flowrate as % of feed to inlet 14 |
100 |
67 |
33 |
2 |
64 |
Temperature [K] |
95.5 |
94.6 |
95.5 |
94 |
96 |
Pressure [Bara] |
1.61 |
1.54 |
1.61 (+ head) |
1.45 |
1.6 (min) |
Physical state |
VAP |
VAP |
LIQ |
VAP |
LIQ |
Impurities: |
|
|
|
|
|
Methane |
10vpm |
5ppb |
55vpm |
0ppb |
6ppb |
Argon |
0.3% |
0.3% |
0.3% |
8% |
100ppb |
Krypton |
7vpm |
0ppb |
25vpm |
0ppb |
0ppb |
KEY: ppb = volumes per billion (thousand million) |
vpm = volumes per million |
1. A process for producing ultra pure oxygen from a gaseous feed containing oxygen,
light impurities and heavy impurities, comprising:
(a) 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;
(b) condensing a first gaseous stream of said second fraction and supplying resulting
condensate to the first column as reflux;
(c) 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, characterised in that:
(i) the second stream is introduced into the second column at a level above which
there are liquid-vapour contact 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 in light impurities and returning
thus formed condensate to the second column as reflux; and
(iii) subjecting a stream of the fraction enriched in light impurities to further
fractionation in at least one column other than said first and second columns and
recovering an argon product therefrom.
2. A process according to claim 1, in which the stream for further fractionation to
recover the light impurity (argon) product is returned to the same column from which
the gaseous oxgyen feed is taken.
3. A process according to claim 2, in which said same column is typically the lower
pressure column of a conventional double column arrangement and 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.
4. A process according to claim 3, 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
5. A process according to any preceding calim, in which the stream taken for further
fractionation contains at least 5% by volume of argon.
6. A process according to any preceding claim, in which the said second stream is
introduced into the said second column as a gas or vapour and not a liquid.
7. A process according to any preceding claim, in 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.
8. A process for producing ultra high purity substantially as herein described with
reference to the accompanying drawings.