Background of Invention
(a) Field of the Invention
The present invention relates to the technology of air distillation to produce argon by means of an apparatus for air distillation with double column. It concerns first a process of the type in which air to be treated, from which water and CO.sub.2 have been removed and cooled at about its dew point, is injected at the base of the mean pressure column of the double column; a first fraction of rich liquid withdrawn at the bottom of the mean pressure column, is expanded and sent into a head condenser of a column for the production of impure argon connected to the low pressure column of the double column; and a second fraction of rich liquid, withdrawn from the lower portion of the mean pressure column is expanded and injected as reflux into the low pressure column.
(b) Description of Prior Art
To ensure certain productions, for example of argon in liquid form, as well as oxygen and nitrogen, also in liquid form, apparatuses for the treatment of air should be provided with a turbine in which a substantial portion of the flow of input air, for example 15 to 17 % of this flow, or an equivalent flow of mean pressure nitrogen, is expanded.
However, this leads to a deterioration of the conditions of distillation in the low pressure column, which results for example in a decrease of the yield of extraction of argon. A direct withdrawing of mean pressure nitrogen has similar consequences.
Summary of Invention
The invention aims at enabling to preserve a high yield of extraction of argon in spite of this unfavourable factor.
For this purpose, it is an object of the invention to provided a process of the type mentioned above, characterized in that:
(a) the second fraction of rich liquid is withdrawn from an intermediate point of the mean pressure column; and
(b) a residual gas of the apparatus is obtained from at least a portion of the rich liquid which is withdrawn at the bottom of the mean pressure column.
It is also an object of the invention to provide an apparatus intended to carry out such process. This apparatus, of the type comprising a double distillation column includes a mean pressure column and a low pressure column, and a column for the production of impure argon connected to the low pressure column and including a head condenser, means to transfer into the head condenser a first fraction of rich liquid withdrawn at the bottom of the mean pressure column, and means to send by reflux, in the low pressure column, after expansion, a second fraction of rich liquid withdrawn from the lower portion of the mean pressure column, is characterized in that:
(a) the second fraction of rich liquid is withdrawn from an intermediate point of the mean pressure column; and
(b) the apparatus comprises auxiliary means to provide a residual gas derived from the apparatus, from at least a portion of the rich liquid withdrawn at the bottom of the mean pressure column.
Brief Description of Drawings
Some embodiments of the invention will now be described with reference to the annexed drawings, in which:
FIG. 1 is a schematic representation of an apparatus for the distillation of air according to the invention; and
FIGS. 2 to 4 are similar views of three variants.
Description of Preferred Embodiments
The apparatus represented in FIG. 1 essentially comprises a double distillation column 1, a column for the production of impure argon 2, and a mixing column section 3. In what follows, the pressures indicated are approximate absolute pressures.
The double column 1 comprises a mean pressure column 4 operating at about 6 .times.10.sup.5 Pa, which is surmounted by a low pressure column 5 operating slightly above 1 .times.10.sup.5 Pa. By means of a vaporizer-condenser 6, the vapor at the top of column 4 (nitrogen) is put into heat exchange with the liquid at the bottom of column 5 (substantially pure oxygen). A so-called argon tapping qas duct connects an intermediate point of the column 5 to the lower portion of column 2, from the bottom of which, a liquid return duct 8 reaches column 5, substantially at the same level. Column 2 includes a head condenser 9.
The air to be separated, which is compressed and free from water and CO.sub.2, for example by adsorption, is injected at the base of column 4. A first "rich liquid"(oxygen enriched air) LR1, consisting of the liquid collected at the bottom of column 4, is removed via duct 10, sub-cooled in a sub-cooler 11, and divided in two flows or fractions:
a first flow is expanded in an expansion valve 12 and entirely vaporized in condenser 9. The resulting gas is sent into column 5 via duct 13;
the remaining portion is expanded in an expansion valve 14 and sent to the top of the column section 3.
The sub-cooler 11 is cooled by natural circulation of oxygen, withdrawn in liquid form from the bottom of column 5 and sent back to the latter after an at least partial vaporization.
A second rich liquid LR2, so-called superior rich liquid, is withdrawn from column 4 a few plates above the bottom, and more specifically close to the level where argon is at a maximum concentration. This liquid, after sub-cooling at 11, is expanded in an expansion valve 15 and sent as reflux to an intermediate point of column 5, above the outlet of duct 13. "Inferior poor liquid", rich in nitrogen, is withdrawn from an intermediate point of column 4 above liquid LR2 and, after expansion, is sent as reflux at the top of column 5, via duct 16.
Impure nitrogen containing a small quantity of oxygen is produced at the top of column 5, and is sent to the base of section 3 via duct 17; a liquid duct 17A runs from the bottom of the same section and ends at the top of column 5.
Thus, column section 3, although structurally similar to a distillation column provided with plates or lining, operates as a mixing column: the liquid which is received at the top contains less nitrogen, and is consequently less cold, than the one which is produced at the bottom, which corresponds to the operation of a heat pump and is obtained by the energy recovered by re-mixing the liquid LR1 and impure nitrogen under conditions close to reversability
Duct 17A thus provides an additional reflux liquid containing little oxygen, at the top of column 5, and the vapor produced at the top of section 3 is removed from the apparatus via duct 18 as residual gas.
The low pressure column 5 is additionally surmounted with a "minaret" 19 which is used for producing pure nitrogen under 1 .times.10.sup.5 Pa. The base of this "minaret" is connected to the top of column 5 and is therefore fed by means of a portion of the impure nitrogen produced by the latter. Its reflux consists of liquid nitrogen supplied via duct 20. Low pressure nitrogen is produced at the top of "minaret" 19 and is removed via duct 21.
The apparatus, on the other hand, may produce gaseous oxygen, liquid oxygen, mean pressure gaseous nitrogen and mean pressure liquid nitrogen, via respective ducts 22 to 25. A portion of the gaseous nitrogen is liquefied by means of an auxiliary lique fraction cycle (not illustrated), and a portion of the liquid nitrogen thus produced feeds duct 20.
As a variant, a portion of the second flow of liquid LR1 (liquid LR1 not vaporized in condenser 9) could be directly sent as reflux after expansion, into column 5.
Impure argon is produced in gas form and is removed from the top of column 2 via duct 26.
The essential elements described above with respect to FIG. 1 are also found in FIG. 2. The differences are the following:
On the one hand, the apparatus does not produce low pressure nitrogen, so that the minaret 19 is omitted. To simplify the construction, the mixing section 3 is then directly disposed above column 5, within the same coupling ring, and ducts 17, 17A and 21 are omitted. Moreover, duct 20 is omitted and the single duct 16 for feeding poor liquid into column 5 opens immediately below the base of section 3. On the other hand, a duct 27 for introducing liquid nitrogen at the top of column 4 has been represented in FIG. 2.
On the other hand, all the rich liquid LR1 is sent, after expansion in valve 12, into condenser 9. In the latter, only a portion of the liquid is vaporized, the resulting gas being sent as previously mentioned into column 5 via duct 13. The nonvaporized liquid, enriched in oxygen, is sent, as previously, to the top of section 3. As indicated previously, a portion of the non-vaporized liquid could be directly sent as reflux into column 5.
The apparatus illustrated in FIG. 3 differs from that of FIG. 1 only by the absence of mixing section 3: the fraction of rich liquid LR1 which is not sent to condenser 9 is directly sent, after expansion in expansion valve 14, into column 5, and the residual gas withdrawn by means of duct 18, consists of at least a portion of the gas resulting from the total vaporization of rich liquid LR1 carried out in the condenser 9, the remaining portion of this gas being, as previously, sent into column 5 via duct 13. A duct 17B enables to withdraw a second residual gas consisting of impure nitrogen from the apparatus, at the top of column 5.
It should be noted that, although it contains more oxygen than liquid LR2, the liquid expanded at 14 is injected into column 5 above the point where liquid LR2 is introduced, because it contains less argon than the latter. This increases the yield of argon of the apparatus.
The apparatus illustrated in FIG. 4 differs from the previous one only by the fact that the entire liquid LR1, after expansion in valve 12, is sent into condenser 9, where it is only partially vaporized. The non-vaporized liquid which is enriched in oxygen, is sent as reflux into column 5 via duct 28, and the gas resulting from vaporization, as shown in FIG. 3, is partially withdrawn from the apparatus as residual gas via duct 18. For the same reason as in FIG. 3, it is the argon content of the liquid that circulates in duct 28 which determines the level where this liquid is injected into column 5.
In the example illustrated, this liquid contains more argon than Liquid LR2, and duct 28 consequently opens below liquid LR2.