This application is a §371 of International PCT Application PCT/FR2007/052486, filed Dec. 12, 2007.
The present invention relates to a method for separating a mixture of carbon monoxide, nitrogen, hydrogen and optionally methane by cryogenic distillation.
All the pressures mentioned are absolute pressures and the percentages are molar percentages.
It is known to separate such a mixture in order to produce carbon monoxide and hydrogen by a methane scrubbing process as described in Linde Reports on Science and Technology, “Progress in H2/CO Low-Temperature Separation” by Berninger, 44/1988 and in “A New Generation of Cryogenic H2/CO Separation Processes Successfully in Operation at Two Different Antwerp Sites” by Belloni, International Symposium on Gas Separation Technology, 1989.
Other documents that describe methane scrubbing processes comprise: EP-A-0928937, U.S. Pat. Nos. 4,478,621, 5,609,040 and Tieftemperaturtechnik, page 418.
The carbon monoxide derived from H2/CO cold boxes entrains with it a large fraction of the nitrogen present in the feed gas. This phenomenon is linked to the difficulty in separating the two components CO and N2, their bubble points being very close. Nevertheless, depending on the use which is made of the CO downstream of the cold box, it sometimes proves necessary to reduce its nitrogen content before exporting it.
In order to do this, recourse has conventionally been made to the installation in the cold box of a column known as a denitrogenation column, the function of which is to produce, at the bottom, carbon monoxide at the required purity. At the top of the column, a nitrogen purge containing a fraction of CO is recovered. The denitrogenation column is installed either upstream, or downstream of the CO/CH4 separation column.
The reboiling of the denitrogenation column is carried out by an injection of carbon monoxide in vapor form in the bottom of the column.
This carbon monoxide comes from several sources, one of which is the vaporization of liquid carbon monoxide at medium pressure in the exchange line. This medium-pressure carbon monoxide is therefore high-pressure carbon monoxide which has been liquefied and will thus have two uses:
It therefore appears advantageous to maximize the portion of medium-pressure carbon monoxide vaporized.
This flow may be limited by two phenomena:
Depending on the case, the flow of vaporized medium-pressure carbon monoxide will therefore be sized by the exchange line or by the maximum admissible fraction in the reboiling of the CO/N2 column. When it is possible to vaporize more medium-pressure carbon monoxide, but when there is limitation due to the reboiling and when this leads to compressing of the medium-pressure carbon monoxide in addition, there is an energy loss (which results in an a priori smaller exchange surface area).
The present invention aims to remove this constraint which leads to a sizeable energy loss on current estimates, and also to eliminate the medium-pressure gas outlet on the compressor which compresses the carbon monoxide to the high pressure (line, filter, valves, passages in the exchangers, controls, etc.).
According to one subject of the invention, a method is provided for separating a mixture of carbon monoxide, nitrogen, hydrogen and optionally methane by cryogenic distillation in a system of separation means comprising a turbine, a methane scrubbing column, a stripping column, a CO/CH4 column and a denitrogenation column, the denitrogenation column being downstream or upstream of the CO/CH4 column in which the mixture is separated in order to obtain a fluid enriched in carbon monoxide and containing nitrogen, this fluid is separated in the denitrogenation column, a flow of carbon monoxide originating from the column system is compressed in a compressor to a high pressure, optionally between 25 and 45 bars, high-pressure carbon monoxide is sent from the compressor to the turbine and from the turbine to the denitrogenation column, a fraction of the high-pressure carbon monoxide flow is used as product and another portion of the high-pressure carbon monoxide, optionally between 25 and 45 bars, is cooled before being expanded, characterized in that at least occasionally a variable amount of the other portion of high-pressure carbon monoxide cooled in a valve is expanded before being sent to the bottom of the denitrogenation column and the flow expanded in the valve is varied as a function of the reboiling needs of the denitrogenation column and a fraction of the high-pressure carbon monoxide, optionally between 25 and 45 bars, is sent to the bottom reboiler of the stripping column and/or of the CO/CH4 column.
According to other optional aspects of the invention, it is provided that:
According to another subject of the invention, an installation is provided for separating a mixture of carbon monoxide, nitrogen, hydrogen and optionally methane by cryogenic distillation in a system of separation means comprising a turbine, a methane scrubbing column, a stripping column, a CO/CH4 column and a denitrogenation column, the denitrogenation column being downstream or upstream of the CO/CH4 column, means for sending the mixture to the system of separation means in order to obtain a fluid enriched in carbon monoxide and containing nitrogen, means for sending this fluid into the denitrogenation column, a compressor, means for sending a flow of carbon monoxide that originates from the column system to the compressor and means for collecting a flow of carbon monoxide at a high pressure at the outlet of the compressor, means for sending a portion of the high-pressure flow to the turbine and from the turbine to the denitrogenation column, means for sending another portion of the high-pressure flow to a bottom reboiler of the stripping column and/or of the CO/CH4 column, means for recovering a fraction of the flow of high-pressure carbon monoxide as product, a heat exchanger where another portion of the high-pressure carbon monoxide is cooled and an expansion valve for the high-pressure carbon monoxide connected to the heat exchanger and to the denitrogenation column, means for varying the flow of high-pressure carbon monoxide expanded in the valve as a function of the reboiling requirements.
Optionally, the installation comprises means for measuring a flow of carbon-monoxide-rich gas sent as bottoms.
For a further understanding of the nature and objects for the present invention, reference should be made to the detailed description, taken in conjunction with the accompanying drawing, in which like elements are given the same or analogous reference numbers and wherein:
The idea is to size the device without the constraint on the fraction of reboiling independent of the medium-pressure carbon monoxide vaporized (and therefore it is accepted that all the reboiling can originate from the vaporization of the medium-pressure carbon monoxide). Next, a line is installed between the high-pressure carbon monoxide outlet to the reboilers of the stripping column and of the CO/CH4 column (around −110° C.) and the feed for the reboiling of the CO/N2 column. This line will therefore lead to the investment in the line itself and in a single valve (there are already valves on the upstream lines (going to the reboilers fed by the high-pressure carbon monoxide) and downstream lines (vaporized medium-pressure carbon monoxide)). The medium-pressure carbon monoxide thus produced does not pass into an exchange line and the flow can therefore be set to zero for operation of the device. During operation, if it is desired to reduce the medium-pressure carbon monoxide vaporized while retaining a higher reboiling flow, it is sufficient to top up via this medium-pressure carbon monoxide.
The advantage of injecting this “back-up” medium-pressure carbon monoxide into the high-pressure carbon monoxide intended for the reboilers of the columns is that the high-pressure carbon monoxide is often hotter than the “supplementary” high-pressure carbon monoxide that exits at the same temperature as the syngas from the first exchanger. The expansion of the high-pressure carbon monoxide to a pressure of around 4 bars (the operating pressure of the CO/N2 column) does not produce liquid. Even if there were some, this would not hinder the operation, it would be sufficient to withdraw more therefrom in order to obtain the correct amount for reboiling.
This invention can be applied generally to any methane scrubbing devices with denitrogenation in the current system. However, when the flow of medium-pressure carbon monoxide that can be vaporized in the exchange line is very substantially smaller than the reboiling flow, it will nevertheless be advantageous to install a medium-pressure outlet on the compressor, to avoid expanding a large flow of the high pressure to the pressure of the column.
It can also be applied generally to any partial condensation devices.
The invention will be described in greater detail while referring to the FIGURE which shows a separation method according to the invention.
In order to simplify the figure, only the inlet of the gas to be treated and the carbon monoxide cycle are shown.
A flow containing carbon monoxide, hydrogen, methane and nitrogen 45 is cooled in the exchanger 9 by heat exchange with a flow of carbon monoxide 1 and is sent to a methane scrubbing column C1 fed at the top by a liquid methane flow at a very low temperature (not illustrated).
However, it will be understood (although it is not illustrated) that the liquid from the bottom of column C1 is sent to the top of the stripping column C2. The overhead gas from column C1 enriched with hydrogen exits the installation. The liquid from the bottom of the stripping column C2 is sent to a CO/methane separation column C3. The liquid from the bottom of column C3 is sent back to the top of column C1. The overhead gas from column C3 is sent to an intermediate point of the denitrogenation column C4 where it is separated into a carbon-monoxide-rich liquid at the bottom and a nitrogen-rich gas at the top. The operation of the columns therefore corresponds essentially to that of the process from FIG. 6 of Linde Reports on Science and Technology, “Progress in H2/CO Low-Temperature Separation” by Berninger, 44/1988.
A flow of impure carbon monoxide 1 at a pressure of 2.6 bar is sent to the compressor V1, V2 in order to be compressed to a pressure between 25 and 45 bar, preferably between 35 and 40 bar in order to form the flow 5. This flow is divided into one portion 7 which constitutes a production and another flow which is sent to the exchanger 9. A fraction 13 passes completely through the exchanger before being divided in two. A first flow 55 is then divided into three flows 19, 21, 23. A first flow 19 is used to reboil the stripping column C2, a second flow 23 is used to reboil the CO/methane column C3, the two flows 19, 23 are thus liquefied and the cooled flows 19, 23 are sent with the third flow 21 to an exchanger 17. The flow 23 is divided in two, one portion 25 being expanded in a valve 27 then vaporized in the exchanger 17 and sent in gas form to the bottom of the denitrogenation column C4. The rest 26 of the flow 23 is expanded to a pressure of 2.6 bars and sent to a separator pot 35 after expansion in a valve. The flows 21, 19 are also expanded in valves and sent to the same separator pot 35.
It will be easily understood that one portion of one of the flows 19, 21 could be vaporized and sent to the bottom of the denitrogenation column C4 in addition to the flow 25 or instead of this flow 25.
The flow 57 of high-pressure carbon monoxide is expanded in a valve 59 and then sent to the bottom of the denitrogenation column C4. The sending of high-pressure carbon monoxide 57 expanded in the valve 59 is triggered if the flow of carbon monoxide gas 15, 25 sent to the denitrogenation column is reduced by at least 5%, or even by at least 10% relative to the nominal flow.
The gas 43 formed in the separator pot 35 is sent back to the compressor V1 after reheating in the exchanger 9.
The liquid from the separator pot 35 is divided into four. One portion 1 is sent to a separator pot 33 where it forms a gaseous fraction 41 and a liquid fraction 31. The liquid fraction 31 is vaporized in the exchanger 17. The gaseous fraction 41 is heated in the exchanger 17 against the flows 19, 21, 23 before being sent back to the compressor V1.
A portion 2 is used to subcool the methane scrubbing column C1 before being mixed with the flow 41.
A portion 3 is used to condense the top of the CO/methane column C3 where it is vaporized and is then sent back to compressor V1.
The fourth portion 37 is mixed with the bottoms liquid 29 from the denitrogenation column and is used to cool the top of this column. The flow formed 39 is sent back to compressor V1.
Finally, a flow 11 is partially cooled in the exchanger 9, is expanded in a turbine T, is cooled in the exchanger 17 as flow 15 and is sent to the bottom of the denitrogenation column C4.
It will be understood that many additional changes in the details, materials, steps and arrangement of parts, which have been herein described in order to explain the nature of the invention, may be made by those skilled in the art within the principle and scope of the invention as expressed in the appended claims. Thus, the present invention is not intended to be limited to the specific embodiments in the examples given above.
Number | Date | Country | Kind |
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06 55770 | Dec 2006 | FR | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/FR2007/052486 | 12/12/2007 | WO | 00 | 6/18/2009 |
Publishing Document | Publishing Date | Country | Kind |
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WO2008/078040 | 7/3/2008 | WO | A |
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2879595 | Jun 2006 | FR |
Entry |
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English translation of abstract for FR2879595. |
Berninger, R., “Fortschritte Bei Der H2/CO-Tieftemperaturzerlegung” Berichte Aus Technik Und Wissenschaft, Linde AG. Wiesbaden, DE, vol. 62, 1988, pp. 18-23. |
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Search Report for PCT/FR2007/052486. |
Berninger, R., “Progress in H2/CO Low-Temperature Separation”, Linde Reports on Science and Technology, vol. 62, 1988, pp. 18-23. |
Number | Date | Country | |
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20100071411 A1 | Mar 2010 | US |