Patent Application
20140305162
The present invention refers to a thermally integrated process and apparatus for the purification and separation of components of a synthesis gas.
The term “synthesis gas” is generally applied to gaseous mixtures which can be used to synthesize other organic compounds. In this particular case, it refers to a mixture of carbon monoxide, hydrogen, carbon dioxide as main components and methane, water, nitrogen, acid gas (CO2), sulphides (H2S, COS), cyanides (HCN), ammonia and heavy hydrocarbons as secondary components.
Coal (or petcoke or residue) gasification is often used to produce synthesis gas, presents many advantages with regards to operating costs and is developing more and more, especially in countries like China.
Acid gases, such as carbon dioxide and hydrogen sulphide contained in the synthesis gas are removed through a purification unit via washing by a solvent. As an example, the Rectisol® unit (RU) is a well known physical wash process to remove acid gases and sulphides in cold methanol (−20° C.; −70° C.). In this process the synthesis gas is first cooled against cold products produced by the purification unit itself, methanol being primarily injected into the synthesis gas to prevent the formation of ice. The synthesis gas is then sent to the bottom of a washing column where hydrogen sulphide and COS are removed by washing with liquid methanol solvent rich in carbon dioxide, coming from the upper part of the column. The carbon dioxide contained in the synthesis gas is absorbed by washing with clean liquid methanol at the top of the column. Purified synthesis gas, which is free from carbon dioxide and COS and hydrogen sulphide, is withdrawn at the top of the column (absorber). The methanol rich in carbon dioxide and sulphur compounds is removed at the bottom of the wash column and regenerated by a series of expansion steps down to a medium pressure, so as to produce a flash gas. The methanol rich in carbon dioxide from the upper section is also regenerated by expansion down to a lower pressure to produce a second flash gas. The medium and low pressure expansions serve to remove the acid gases from the solvent. The solvent is then further regenerated by warm regeneration so as to produce clean methanol.
The purified gas leaving the top of the absorber is then further purified by adsorption and sent to a cold box where it may be treated by washing with liquid nitrogen, liquid carbon monoxide or liquid methane or by partial condensation.
Flash gas from the cold box may be produced from a phase separator of a partial condensation step or from an intermediate distillation column.
“Low Temperature Technology in Coal Refining” by W. H. Scholz, Chemical Economy and Engineering Review, Vol 14, January 1982 suggests that an ammonia synthesis gas could be warmed in a Rectisol® plant.
One aim of the present invention is to optimize the heat balance (integration of cold) between the purification unit and the cold box.
According on an object of the invention, there is provided a process for the purification and separation of a synthesis gas stream containing hydrogen, carbon monoxide and carbon dioxide in which synthesis gas is purified in a purification unit involving a methanol washing step to remove at least carbon dioxide, the carbon dioxide depleted synthesis gas is purified by adsorption to produce a purified synthesis gas stream and the purified gas stream is sent to a cryogenic unit where it is cooled and separated by cryogenic separation in a column system to produce at least one stream enriched in carbon monoxide, at least one said stream enriched in carbon monoxide is divided in two, one part of the stream being removed from a column of the cryogenic separation unit as a first stream, the other part of the stream forming a second stream and being sent to the purification unit wherein it is warmed and the warmed second stream is mixed with the first stream.
Optionally:
According to a further object of the invention, there is provided an apparatus for the purification and separation of a synthesis gas stream containing hydrogen, carbon monoxide and carbon dioxide including a purification unit comprising a methanol washing column and at least one heat exchanger, wherein synthesis gas is purified to remove carbon dioxide, an adsorption unit wherein the carbon dioxide depleted synthesis gas from the purification unit is further purified by adsorption to produce a purified synthesis gas stream, a cryogenic separation unit wherein the purified synthesis gas stream from the adsorption unit is cooled and separated by cryogenic separation in a column of a column system to produce at least one stream enriched in carbon monoxide, means for removing said at least one stream enriched in carbon monoxide from a column of the column system, a heat exchange line for warming the stream, means for dividing the stream into a first stream and a second stream, means for removing the first stream from the cryogenic separation unit, means for removing the second stream from the cryogenic separation unit, means for sending the second stream to the heat exchanger of the purification unit and means for removing the warmed second stream from the heat exchanger and mixing it with the first stream.
Optionally:
These and other features, aspects, and advantages of the present invention will become better understood with regard to the following description, claims, and accompanying drawings. It is to be noted, however, that the drawings illustrate only several embodiments of the invention and are therefore not to be considered limiting of the invention's scope as it can admit to other equally effective embodiments.
The invention will be described in greater detail with reference to the attached figures.
In
Synthesis gas 1 from a synthesis gas generation unit (not shown—gasifier as an example) is cooled in a heat exchanger 3 and sent to a purification unit W which uses a solvent washing step (methanol as an example). The synthesis gas is treated in unit W to remove acid gases, such as carbon dioxide and hydrogen sulphide. The purified synthesis gas 7 at −65° C. to −35° C. is sent to an adsorption unit P, to remove solvent and carbon dioxide traces, forming gas 11. Gas 11 at between −35° C. and −65° C. is divided into two parts. One part 11 is used to cool the synthesis gas in exchanger 3. The synthesis gas 11 is thereby warmed to a temperature around ambient, i.e. between 0° C. and 45° C. and is then sent to the cryogenic distillation unit C where it is cooled down from the ambient temperature in warm heat exchanger HX and cold heat exchanger CX before being separated by cryogenic distillation in a column system to form a product gas 13, such as carbon monoxide and a further gas 15 which is a flash gas or a purge gas, each gas being removed from a column of the column system.
The rest of gas 11 from adsorption unit P forms parts 11A which is warmed up in the purification unit W to form warmed gas 11A which is mixed with warmed gas 11 from exchanger 3 and is sent at ambient temperature to the cryogenic distillation. Gas 13A is formed by a portion of the product gas 13 of the cryogenic distillation unit but removed from the warm heat exchanger HX at between −65° C. to 20° C. Gas 13A is warmed in heat exchanger 3 against the feed synthesis 1 Gas 13B is a portion of gas 13B, warmed in the purification unit and mixed with Gas 13A; The mixture is sent to the warm heat exchanger HX or downstream of the heat exchanger HX outside the cryogenic unit C.
Similarly a portion 15A of gas 15 is removed from the warm heat exchanger HX and/or the cold heat exchanger CX at between −65° C. to 20° C. and divided in two, part 15B being warmed in the purification unit W and part 15A being warmed in exchanger 3. The rest of stream 15 is warmed in heat exchanger HX to form a purge gas. The two warmed streams are mixed to form stream 15A and sent back to stream 15. The mixing point is either within the warm heat exchanger HX via stream 15C or downstream of the heat exchanger HX outside the cryogenic unit C.
The raw synthesis gas 101 is cooled in a series of heat exchangers 103, 105, 113. In the first heat exchanger 103, the raw feed gas is cooled against cold synthesis gas A coming from the cryogenic unit C, for example a liquid nitrogen wash unit, and against the purified gas 112 exiting the H2S/CO2 absorption column K01. In the second heat exchanger 105, the raw feed gas is cooled against colder fluid A from the cryogenic unit. The condensed water and BTX/naphtha are then separated in a gas separator 107 and sent to battery limits. Water is removed from the feed gas in order to avoid water build-up in the methanol loop: if the water content is too high, solubility of methanol drops. A water wash column 109 is included to remove NH3. The gas 111 is sent to a third cooling step in exchanger 113. In the exchanger 113, the gas 111 is then further cooled against gas A from the cryogenic unit C, against the purified gas 112 exiting the H2S/CO2 absorption column K01 and against CO2 product 141 coming from the re-absorber CO2 product column K03. Additionally the gas may be cooled against recycle top gas 127 coming from the MP flash column K02. The cooled gas 111 is then sent to the H2S/CO2 absorption column K01.
The gas is sent to the bottom pre-wash section of the absorption column K01 where trace components like NH3, and HCN and BTX are absorbed with a small stream of CO2-sub-cooled-laden methanol. The pre-wash methanol 115 leaves the bottom of the absorption column K01 and is sent to the hot regenerator column K04.
The synthesis gas is then routed up via a chimney tray into the H2S-absorption section of the absorption column K01 (bottom section) where H2S and COS are removed by dissolution in CO2-saturated methanol coming from the CO2-absorbtion section (top section). The methanol solvent is fed to the top of the Absorption section on flow control proportional to the inlet gas flow. The CO2+H2S-laden methanol 116 leaves the main sump of the absorber column K01 and is routed to the MP-Flash Column K02 for regeneration. The de-sulfurised gas then enters the lower washing part of the CO2-absorption section via another chimney tray. An additional sulphur-free feed gas stream may also be fed to the column at this point.
In the CO2-absorption section, the gas is washed with cold, flash regenerated methanol used as main wash methanol and with cold, hot regenerated methanol used as fine wash methanol. Due to the heat of absorption of the CO2, the methanol 117, 123 is heated up considerably and needs to be cooled on its way down the column. Therefore, in the lower part of the CO2-absorbtion section, the gas is scrubbed with CO2-laden methanol which is cooled against gas A from the cryogenic unit C in exchangers 119, 121. The cold purified gas 112 exiting the absorber K01 is then routed to the adsorption unit P of
The bottom liquid 135 from flash column K02 is sent to the top of column K03 following cooling in exchanger 136 against stream A.
The LP flash column K03 receives the bottom liquid 135 and 137 from column K02 and produces a CO2 rich stream 141 and an off-gas stream, which is sent to the atmosphere. In hot regenerator K04 the methanol is finally regenerated by stripping with methanol vapours. The overheads being an acid gas with sulphur content suitable to be processed in a Claus sulphur recovery unit. The bottoms product, stream 125, is the finewash methanol fed on top of absorber K01.
The stream A is thus used to cool at least one of the following fluids: methanol removed at an intermediate point of the absorption column K01, synthesis gas which is to be treated in absorption column K01, bottom liquid from the MP flash column K02, which then feeds the LP flash column K03.
Among the advantages of the invention are:
While the invention has been described in conjunction with specific embodiments thereof, it is evident that many alternatives, modifications, and variations will be apparent to those skilled in the art in light of the foregoing description. Accordingly, it is intended to embrace all such alternatives, modifications, and variations as fall within the spirit and broad scope of the appended claims. The present invention may suitably comprise, consist or consist essentially of the elements disclosed and may be practiced in the absence of an element not disclosed. Furthermore, if there is language referring to order, such as first and second, it should be understood in an exemplary sense and not in a limiting sense. For example, it can be recognized by those skilled in the art that certain steps can be combined into a single step.
The singular forms “a”, “an” and “the” include plural referents, unless the context clearly dictates otherwise.
“Comprising” in a claim is an open transitional term which means the subsequently identified claim elements are a nonexclusive listing (i.e., anything else may be additionally included and remain within the scope of “comprising”). “Comprising” as used herein may be replaced by the more limited transitional terms “consisting essentially of” and “consisting of” unless otherwise indicated herein.
“Providing” in a claim is defined to mean furnishing, supplying, making available, or preparing something. The step may be performed by any actor in the absence of express language in the claim to the contrary a range is expressed, it is to be understood that another embodiment is from the one.
Optional or optionally means that the subsequently described event or circumstances may or may not occur. The description includes instances where the event or circumstance occurs and instances where it does not occur.
Ranges may be expressed herein as from about one particular value, and/or to about another particular value. When such particular value and/or to the other particular value, along with all combinations within said range.
All references identified herein are each hereby incorporated by reference into this application in their entireties, as well as for the specific information for which each is cited.
| Number | Date | Country | Kind |
|---|---|---|---|
| 11306476.0 | Nov 2011 | EP | regional |
This application is a §371 of International PCT Application PCT/EP2012/072522, filed Nov. 13, 2012, which claims the benefit of EP11306476.0, filed Nov. 14, 2011, both of which are herein incorporated by reference in their entireties.
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP2012/072522 | 11/13/2012 | WO | 00 | 5/14/2014 |
