METHOD AND APPARATUS FOR LIQUEFYING A GAS RICH IN CARBON DIOXIDE

Abstract

A method for liquefying a CO2-rich gas flow containing at least 90 mol % of CO2 involves the following steps: compressing the CO2-rich gas flow, liquefying and separating in order to produce a first liquid flow at a first pressure MP and a first temperature T1. Extracting part of the first liquid flow at the first pressure and the first temperature by way of first product, supercooling part of the first liquid flow down to a temperature below the first temperature by indirect exchange of heat in a heat exchanger, expanding the liquid supercooled down to the second temperature T2 until it reaches a second pressure lower than the first pressure, the second pressure being equal to or greater than the equilibrium pressure of the expanded liquid, and extracting part of the expanded liquid by way of second product and evaporating another part of the liquid in the heat exchanger by exchange of heat with the part of the first flow in order to produce a vaporized liquid.

Claims

1-14. (canceled)

15. A method for liquefying a gas flow rich in CO.sub.2 containing at least 90 mol % of CO.sub.2 comprising the following steps: a) compression and possibly drying of the gas flow rich in CO.sub.2 in a compressor b) liquefaction and separation by distillation and/or phase separation to produce a first liquid flow at a first pressure MP and a first temperature T1 c) extraction of a portion of the first liquid flow at the first pressure and the first temperature as a first product d) subcooling of a portion of the first liquid flow to a temperature below the first temperature by indirect heat exchange in a heat exchanger e) expansion of a portion of the subcooled liquid to a second pressure below the first pressure to form a second product f) expansion of the remainder of the subcooled liquid to a third pressure and vaporization of the remainder of the expanded in the heat exchanger by heat exchange with the portion of the first flow to produce a vaporized liquid, and potentially g) recycling of at least a portion of the vaporized liquid flow to step and/or step.

16. The method as claimed in claim 15, wherein the first pressure is greater than 14 bar.

17. The method as claimed in claim 15, wherein the first temperature is up to 5? C. less than the equilibrium temperature or equal to the equilibrium temperature.

18. The method as claimed in claim 15, wherein the second pressure is equal to or less than 10 bar.

19. The method as claimed in claim 15, wherein the second temperature is up to 5? C. less than the equilibrium temperature or equal to the equilibrium temperature.

20. The method as claimed in claim 15, wherein vaporized gas in the heat exchanger transfers cold to the gas flow rich in CO.sub.2.

21. The method as claimed in claim 15, wherein the heat exchanger exchanges heat between the expanded liquid and the portion of the first liquid flow only.

22. The method as claimed in claim 15, wherein the compressor compresses the flow rich in CO.sub.2 to at least 60 bar, the flow at at least 60 bar is cooled in a second heat exchanger to a temperature below 35? C. before being liquefied.

23. The method as claimed in claim 15, wherein vaporized gas in the heat exchanger is conveyed to a point upstream of the liquefaction of the gas flow, for example an inter-stage point of the compressor, which performs the compression step.

24. The method as claimed in claim 15, wherein the third pressure is less than the second pressure.

25. The method as claimed in claim 24, wherein the third pressure is between 5 and 6 bar.

26. A method for modifying an apparatus for liquefying a gas flow rich in CO.sub.2 containing at least 90 mol % of CO.sub.2, wherein the apparatus comprises: a) a compressor and means for conveying the gas flow rich in CO.sub.2 to the compressor b) liquefying means connected to the compressor to liquefy the gas flow rich in CO.sub.2 and means of separation by distillation and/or phase separation to separate the liquefied gas flow to produce a first liquid flow as an end product at a first pressure MP and a first temperature T1; wherein the method comprises the steps of: adding the following components to the apparatus: a heat exchanger, means for conveying a portion of the first liquid flow to cool in the heat exchanger, means for expanding a first portion of the first liquid cooled in the heat exchanger and for outputting said expanded liquid as a second end product, and means for expanding a second portion of the first cooled liquid, separately from the first portion of the first liquid, connected to the heat exchanger to enable a heat exchange between the first liquid and the portion of the first expanded liquid.

27. The method as claimed in claim 26, wherein the step of adding the following components to the apparatus includes adding means for conveying at least some of the portion of the heated expanded first liquid in the heat exchanger to the compressor or to another compressor to be compressed.

28. The method as claimed in claim 26, wherein a dedicated compressor compresses the heated expanded first liquid.

Description

[0036] FIG. 1 shows an apparatus to be modified to implement a method according to the invention.

[0037] FIG. 2 shows an apparatus for implementing a method according to the invention.

[0038] FIG. 3 shows a variant of [FIG. 2].

[0039] FIG. 4 shows a variant of [FIG. 2].

[0040] FIG. 5 shows a variant of [FIG. 4].

[0041] FIG. 6 shows an apparatus to be modified to implement a method according to the invention.

[0042] FIG. 7 shows an apparatus for implementing a method according to the invention.

[0043] FIG. 1 shows an apparatus used to liquefy a flow rich in carbon dioxide that can produce a single product 11 at a first pressure and a first temperature. The first pressure is preferably greater than 14 bar, preferably between 15 and 19 bar.

[0044] The first temperature is up to 5? C. less than the equilibrium temperature or equal to the equilibrium temperature.

[0045] A gas 1 containing at least 80 mol %, preferably at least 95 mol %, of carbon dioxide as well as impurities, such as carbon monoxide, nitrogen or oxygen, is compressed in the first portion C2 of a compressor, comprising at least one stage. Said gas is subsequently compressed in the second portion C3 of the compressor, comprising at least one stage, to reach a pressure greater than the critical pressure.

[0046] The gas 3 is liquefied and separated in a unit H1, for example by distillation and/or by partial condensation in a phase separator to eliminate light and/or heavy impurities in the gas 1, 3. The formed liquid 5 is expanded in a valve V2 to form the product 11.

[0047] The compressor C1 may be used as required to meet product specifications and expected yield, and is provided upon installation of the apparatus in [FIG. 2] with a view to future modification. This compressor C1 can be the first stage of a compressor C1, C2, C3 or can be a standalone compressor.

[0048] FIG. 2 shows how the apparatus in [FIG. 1] is modified to enable the production of a second product 17 at a second pressure below the first pressure and at a second temperature, preferably from the same feed flow. The second pressure is preferably equal to or less than 10 bar, for example between 6 and 8 bar.

[0049] The second temperature is preferably up to 5? C. less than the equilibrium temperature or equal to the equilibrium temperature.

[0050] The liquid expanded in the valve V2 is separated into two, with one portion forming the first product 11 and the remainder 13 being conveyed to a heat exchanger H2 using indirect heat exchange, for example a plate-and-fin heat exchanger made of brazed aluminum.

[0051] The liquid 13 is cooled in the exchanger H2 to form a subcooled liquid 15, which is expanded in a valve V3 to form the product 17.

[0052] A portion of the subcooled liquid 15 is expanded in a valve V4 to be cooled in order to provide the energy required to cool the liquid 13 during vaporization in H2. The formed flow 21 is returned to the compressor C1. The formed flow is then mixed with the gas 1 and is further compressed in stages C2, C3.

[0053] The flow 21 can be conveyed in full or in part for compression and/or liquefaction and/or separation. Some or all of the flow can also be left unrecycled.

[0054] Where recycling is provided for, the elements in [FIG. 1] are dimensioned in consideration of the future modifications in [FIG. 2], in particular the compressor C2, C3 is dimensioned to enable the recycled flow 21 to be possibly compressed.

[0055] FIG. 3 shows a variant of [FIG. 2] in which the liquid 13 is withdrawn upstream of the valve V2 in order to optimize energy consumption and in consideration of constraints related to the technology of the exchanger H2 with two-phase fluids.

[0056] The flow 5 is thus split into two upstream of the valve V2 to form the flow 13 to be conveyed to the heat exchanger H2 and the flow 11 to be expanded in the valve V2 to form a product.

[0057] FIG. 4 is a variant of [FIG. 2] in which the liquid 5 is conveyed in full to an intermediate storage unit 100 that is preferably acquired at the beginning of the life cycle of the liquefaction unit (see [FIG. 1]) to produce a liquid product 11 rich in CO.sub.2 at a first pressure withdrawn from the storage unit 100. The liquid 13 is withdrawn from the storage unit 100 to be conveyed to H2 to produce the CO.sub.2 product at a second pressure below the first pressure.

[0058] FIG. 5 is a variant of [FIG. 4] that enables the vapor phase 22 at the top of the storage unit 100 to be treated if the liquid in the storage unit 100 is partially vaporized as a result of heat input or changes in equilibrium. The gas 22 is conveyed to the exchanger H2 to be cooled and liquefied to form a liquid 23 at a second pressure. This liquid 23 can be mixed with the fluid 15 to form the product or vaporized with or without the flow 19.

[0059] FIG. 6 shows an apparatus used to liquefy a flow rich in carbon dioxide that can produce a single product 11 at a first pressure and a first temperature. The apparatus is similar to [FIG. 1], but does not include the compressor C1 previously provided.

[0060] Following compression, the gas 3 is cooled in a cooler CW by a refrigerant, the temperature of which is liable to change with the ambient temperature, for example air or water, to form a supercritical gas 3 with a density between 370 and 900 kg/m3. The gas is cooled in a shell-and-tube or brazed-aluminum-plate heat exchanger 6 to reach a subcritical temperature, for example between 5? C. and 25? C. The formed fluid 4 is expanded in a valve 50 to a pressure between 45 and 60 bar to form a two-phase fluid that is subsequently separated in a phase separator 60.

[0061] A portion 8 of the liquid in the phase separator 60 is used to cool the first heat exchanger 6. In this example, the liquid 8 vaporizes in the exchanger 6 and is returned to the gas to be separated 1 between the two portions C2, C3 of the compressor.

[0062] Otherwise, cold can be transferred to the heat exchanger using other means, and thus the liquid 8 is not necessarily itself conveyed into the first exchanger 6.

[0063] Another portion 11 of the liquid in the phase separator 60 forms the sole product of the apparatus in this figure, at a first pressure and a first temperature.

[0064] Separation by partial condensation in the phase separator 60 can be replaced with distillation in a distillation column, the overhead gas from the distillation column containing light impurities and the bottom liquid in the column forming the portions 8, 11, including the first product.

[0065] Naturally, more complex methods using partial condensation and distillation or distillation involving several columns could be used.

[0066] The portion of the apparatus indicated as H1 is the unit H1 in [FIG. 1].

[0067] FIG. 7 shows [FIG. 6] modified to enable the production of a second product 17 at a second pressure below the first pressure and at a second temperature. This modification involves adding the line 13, the heat exchanger H2, the valves V3, V4, and the lines 15, 17, 19.

[0068] Thus, a portion 13 of the bottom liquid in the phase separator 60 is cooled in the heat exchanger H2 to form the cooled liquid 15. This liquid is separated into two. A portion 17 is expanded in V3 to the second pressure and the second temperature to form the second product. The remainder 19 is expanded in the valve V4 to a third pressure, lower than the second pressure, for example between 5 and 6 bar, to be cooled, is vaporized in the heat exchanger 19 to form the gas 21, and conveyed to the compressor C2.

[0069] This addition of a single module, described for [FIG. 2] and [FIG. 7], makes it possible to obtain a second product by slightly modifying the original layout. The heat exchanger H2, which enables an indirect heat exchange between just two fluids, is cheap and easily available, for example a plate-and-fin exchanger or a shell-and-tube exchanger.

[0070] The vaporized gas 21 can be returned to any suitable point of the method, for example upstream of the compressor C2, downstream of C2 and upstream of C3, downstream of C3 and upstream of H1 or 50 downstream of CW and upstream of 6.

[0071] Where necessary or where the equipment is not dimensioned to recover the vaporized gas 21, a dedicated compressor C4 (not shown) can similarly be added to compress the gas 21 to a suitable pressure to be injected back into a suitable point of the method.

[0072] The flow 21 can be conveyed in full or in part for compression and/or liquefaction and/or separation. Some or all of the flow can also be left unrecycled.

[0073] Where recycling is provided for, the elements in [FIG. 6] are naturally dimensioned in consideration of the future modifications in [FIG. 7], and in particular the compressor C2, C3 is dimensioned to enable the recycled flow 21 to be possibly compressed.