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    • 专利摘要:
    The invention relates to a method and a system for the treatment of exhaust gases (4) from plants (32, 33) for pig iron production and / or synthesis gas, wherein a first substream (51) of the exhaust gas or synthesis gas after addition of water and / or water vapor ( 10) is subjected to at least partial conversion of CO to CO 2 and the waste gas or synthesis gas (4) is subsequently subjected to CO 2 precipitation. In order to be able to set a variable H2 / CO ratio in the exhaust gas or synthesis gas, it is provided that a further substream (52) of the exhaust gas or synthesis gas is not subjected to conversion of CO into CO 2, but separately from the first substream (51) of a CO 2 Deposition.
    公开号:AT511892A1
    申请号:T1245/2011
    申请日:2011-08-31
    公开日:2013-03-15
    发明作者:
    申请人:Siemens Vai Metals Tech Gmbh；
    IPC主号:
    专利说明:

    1 2010 26014 * * · # * · · · ι · * t · · * * * * «* *» «* * * * * •« · »· ·
    description
    Process for the treatment of exhaust gases from pig iron production plants and / or synthesis gas
    FIELD OF THE INVENTION
    The invention relates to a method and a device for the treatment of exhaust gases from plants for the production of pig iron and / or synthesis gas, wherein a first partial stream of the exhaust gas or synthesis gas after addition of water and / or steam is subjected to an at least partial conversion of CO into CO2 and the Exhaust gas or synthesis gas is then subjected to a CQ2 deposition.
    STATE OF THE ART
    For the production of pig iron, which should also include the production of pig iron-like products, there are essentially two known common processes: the blast furnace process and the smelting reduction.
    The blast furnace process first produces pig iron from iron ore using coke. In addition, scrap can also be used. Thereafter, steel is produced by further processes from pig iron. The iron ore is used as lump, pellets or sinter together with the reducing agents (usually coke, or coal, for example in the form of a
    Fine coal indisposition plant) and other constituents (limestone, slag formers, etc.) are mixed to form the so-called Möller and then charged into the blast furnace. The blast furnace is a metallurgical reactor in which the Möllersäule reacts in countercurrent with hot air, the so-called hot blast. By burning the carbon from the coke, the necessary heat for the reaction and carbon monoxide or hydrogen, which constitute a substantial part of the reducing gas, wherein the reducing gas flows through the Möllersäule and the
    SUBSEQUENTLY 2 2010 26014 ♦ # * · ··· · fM «* • *« «« »*« · · · «····· · ·
    Iron ore reduced. The result is pig iron and slag, which are tapped periodically.
    In the so-called oxygen blast furnace, which is also referred to as blast furnace with top or top gas recirculation, in the gasification of coke or coal oxygen-containing gas with more than 90 vol% oxygen content (O2) is injected into the blast furnace. For the gas leaving the blast furnace, the so-called top or blast furnace gas, a gas purification must be provided (for example, dust collectors and / or cyclones in combination with wet scrubbers, bag filter units or hot gas filters). Furthermore, the oxygen blast furnace usually a compressor, preferably with aftercooler, provided for the top gas returned to the blast furnace and a device for CC> 2 removal, according to the prior art usually by means of pressure swing adsorption.
    Further options for the design of an oxygen blast furnace process are a heater for the reducing gas and / or a combustion chamber for the partial combustion with oxygen.
    The disadvantages of the blast furnace are the demands on the feedstock and the high emission of carbon dioxide. The iron carrier used and the coke must be lumpy and hard, so that sufficient cavities remain in the Möllersäule, which ensure the flow through the blown wind. C02 emissions represent a heavy environmental impact. Therefore, there are efforts to replace the blast furnace route. These include iron sponge production based on natural gas (MIDREX, HYL, FINMET ©) and smelting reduction processes (COREX © and FINEX © processes).
    In smelting reduction, a melter gasifier is used, in which hot liquid metal is produced,
    SUBSIDIARY 3 2010 26014 • ···················································· and at least one reduction reactor in which the carrier of the iron ore ( Lump, fine ore, pellets, sinter) with reducing gas, the reducing gas being produced in the melter gasifier by gasification of coal (and optionally a small proportion of coke) with oxygen (90% or more).
    Also in the smelting reduction process are usually
    Gas purification systems (on the one hand for the top gas from the reduction reactor, on the other hand for the reduction gas from the melter gasifier), a compressor, preferably with aftercooler, for the reducing gas recycled in the reduction reactor reducing gas, a device for CO 2 removal, according to the prior art usually by pressure swing Adsorption and optionally provided a heater for the reducing gas and / or a combustion chamber for partial combustion with oxygen.
    The COREX® process is a two-stage process
    Smelting reduction. The smelting reduction combines the process of indirect reduction (prereduction of iron to sponge iron, often referred to as direct reduction) with a melting process (main reduction).
    The well-known FINEX © process essentially corresponds to the COREX® process, but iron ore is introduced as fine ore and prereduced in several fluidized bed reactors in succession.
    The invention can be applied not only to pig iron production but also to synthesis gas plants. Synthesis gases are all hydrogen-containing and mostly CO-containing gas mixtures that are to be used in a synthesis reaction. Synthesis gases can be made from solid, liquid or gaseous substances. In particular, this includes coal gasification (coal becomes
    SUBSCRIPTION 4 2010 26014
    * ··························································································································································································································· and CO implemented) and the production of synthesis gas from natural gas {conversion of methane with water vapor and / or oxygen to hydrogen and CO).
    For the separation of CO 2 from the exhaust gases of
    Pig iron production or from synthesis gases is primarily the pressure swing adsorption (PSA - Pressure Swing Adsorption), especially the vacuum
    Pressure swing adsorption (VPSA) used. Pressure swing adsorption is a physical process for the selective decomposition of gas mixtures under pressure. It belongs to the state of the art and therefore need not be explained further here. Of course, other chemical or physical processes for CO 2 deposition can be used in the subject invention.
    The product gas stream from the CO 2 separation, which contains the valuable substances, can be returned to the pig iron production. After the pressure swing adsorption of exhaust gases from pig iron production, it still contains about 2-6 vol% CO 2 and is typically composed as follows:
    Compound vol% for PSA H2 42 N2 10 CO 4 5 C02 1 CH4 2 h2o 0
    The residual gas stream (tail gas) from the C02 separation still contains relatively high reducing gas constituents {such as CO, H2), which can also be used again for pig iron production, and is becoming established
    ADVANCED 5 2010 26014 * * »· · · ft · · * * · * * ft * * * ft * #« «« · · · #
    Exhaust gases from pig iron production according to a (V) PSA plant are typically composed as follows:
    vol% at VPSA vol% 2.2 5.5 1.5 2.4 10.9 16.8 82.1 72.2 0.7 0.9 2.6 2.2 for PSA
    Connection H2 n2
    CO co2 ch4 h20
    Often, the residual gas can not simply be thermally recycled because - due to the low and / or fluctuating calorific value of about ± 50% - it would have to be enriched with other fuels. For example, it can be wholly added to the so-called export gas, which is the part of the process gas that is withdrawn from the process of pig iron production and used for other purposes, such as fuel in a combined gas and steam power plant, which is also used as a combined cycle power plant. : combined cycle power plant, CCPP for short). Components of the export gas can be: Topgas from a blast furnace, a reduction reactor, which is designed as a fluidized-bed reactor or as a reduction shaft (fixed bed reactor), so-called offgas from a reduction reactor (fluidized-bed reactor), so-called excess gas from a melter gasifier
    In order to increase the hydrogen content in the exhaust gas stream of the pig iron production or in the synthesis gas or in the product gas stream after the CO 2 deposition in relation to the content of carbon monoxide (CO), and thereby to allow the use of the exhaust gas or synthesis gas or the product gas thereof as a reducing gas is in
    NACHGERBCHT 2010 26014 and US Pat. No. 5,676,732 A, as well as WO 2009/08123 A2, in which in addition to the CO 2 deposition, a CO conversion by means of a so-called water gas shift reactor (WGSR) perform. There, the so-called water gas shift reaction takes place, in which CO is converted by the addition of water (vapor) to free hydrogen H2 and CO2. It is an exothermic reaction and is a process for reducing the CO content in the gas and for generating hydrogen. With the aid of catalysts, the reaction can be accelerated.
    In US Pat. No. 5,676,732 A, the entire export gas from a reduction shaft, such as a C0REX® system, is subjected to a CO to carbon dioxide CO 2 conversion. This has the disadvantage that it requires high amounts of steam due to the necessary water vapor excess, about 300 t / h in the case of a COREX® plant. The high hydrogen content leads to a limitation of pig iron productivity and also requires high reduction gas temperatures.
    According to WO 2009/08123 A2, only a part of the exhaust gas from the reduction reactors is subjected to a conversion of CO to CO 2, namely that which is recycled to the reducing gas after the melter gasifier 10, while another part of the exhaust gas from the reduction reactors without conversion CO in carbon dioxide C02 is withdrawn as export gas from pig iron production.
    Also in AT 507 713 Bl, where the waste gas from smelting reduction plants (COREX®, FINEX ©) and oxygen blast furnaces is treated, only part of the flue gas from the reduction reactors is subjected to CO to CO 2 conversion, namely to the oxygen blast furnace or CO 2 is recycled to the reducing gas after the melter gasifier as a reducing gas.
    For other uses of the exhaust gas from the reduction reactors, such as for a direct reduction plant, an exhaust gas with a higher carbon content would again be necessary, but according to the methods of WO 2009/08123 A2 and AT 507 713 Bl At a given time only an exhaust gas with a certain H2 / CO ratio can be produced.
    It is therefore an object of the invention to provide a method with which the exhaust gas from plants for the production of pig iron or synthesis gas can be made available at a given time with different H2 / CO ratio.
    PRESENTATION OF THE INVENTION
    The object is achieved by a method according to claim 1, in that in addition to the first partial flow of the exhaust gas or synthesis gas, which is subjected to the addition of water and / or water vapor at least a partial conversion of CO in CO 2 and then a CO 2 deposition, another partial flow of the exhaust gas or synthesis gas is not subjected to conversion of CO into carbon dioxide CO 2, but is subjected to CO 2 separation separately from the first substream.
    In this case, the first and second partial streams can either originate from the same source and thus have the same composition, see, for example, FIG. 1, or come from different sources and therefore generally have different compositions, see, for example, FIG The second partial stream may contain only waste gas from pig iron production plants, only synthesis gas, or both waste gas from pig iron production plants and synthesis gas, the latter occurring more rarely in practice.
    The exhaust gas / synthesis gas of the first substream after the conversion of CO into CO 2 is more hydrogen-rich than that of the
    SUBSEQUENTLY 8 2010 26014 • * «» Ψ m m ψ · · »· * second partial flow, which is not subject to any conversion of CO into CO 2. Consequently, the product gas after the CO 2 separation of the first partial flow is more hydrogen-rich than that after CO 2 separation of the second partial flow. The product gas from the second partial stream can therefore - apart from the application for reduction in the blast furnace or smelting reduction process - also be used for carburizing and controlling the carbon content in a direct reduction plant, namely for carburizing and controlling the carbon content in the product (DRI - direct reduced iron, HBI hot briquetted iron, LRI - low reduced iron) of the direct reduction plant. For this purpose, the product gas can be introduced into the cooling gas circulation or above the cooling zone, preferably into the so-called transition zone between the reduction zone and the cooling zone, of the reduction reactor, that is to say the reduction shaft of the direct reduction plant.
    On the other hand, the residual or tail gas can hardly be burned alone and without additional preheating after CO 2 separation in the first partial flow due to the low calorific value. It is therefore best added to the rest of the export gas. The residual gas or tail gas after the CO 2 separation in the second partial flow can be used for combustion, for example in the reduction gas furnace of a direct reduction plant, because of the higher calorific value compared to the residual gas of the first partial flow.
    It can also be provided that the residual gas after the CO 2 separation in the first partial flow and the residual gas after the CO 2 separation in the second partial flow are mixed with one another, for example in order to determine the calorific value of the residual gas. for thermal utilization.
    In this invention, the exhaust gas from a blast furnace, in particular an oxygen blast furnace, from a smelting reduction plant, such as a COREX® or EINEX® plant, or from a
    FOLLOW-UP 9 2010 26014 ψ * * * »» · ·········································································· »
    Direct reduction plant, in particular a direct reduction composite system consisting of COREX® plant and direct reduction plants, used.
    Consequently, the exhaust gas contains at least one of the following gases: top gas from a blast furnace, in particular from an oxygen blast furnace with top gas recirculation, or a reduction shaft from a smelting reduction plant exhaust gas from a melter gasifier of a smelting reduction plant, which is also referred to as excess gas, exhaust gas from at least one fluidized bed reactor, which is also referred to as offgas, - exhaust gas from at least one fixed bed reactor for preheating and / or reduction of iron oxides and / or iron briquettes of a smelting reduction plant, which is also referred to as top gas, - exhaust gas of the plant for pig iron production associated C02-deposition plant, - exhaust at least one reduction reactor of a direct reduction plant.
    In a direct reduction plant lumpy iron ore carriers (lump ore, fine ore or pellets (fine-grained iron ore is rolled with water, binders and aggregates to green pellets and hardened in a final firing)) in the solid state at 750-1000 ° C reduced by reducing gas or coal. The result is directly reduced iron (English: direct reduced iron, short DRI), which is also referred to as sponge iron.
    The direct reduction plant contains as its core a reduction reactor, which is designed either as a reduction shaft in the sense of a fixed bed reactor or in the form of fluidized bed reactors into which or into which the lumpy iron ore and the reducing gas (or coal) are introduced.
    FOLLOW-UP 10 2010 26014 «*« * · * «* * * * • * 1 *» l * lf ft ft tfp tftftft
    But a direct reduction plant can also produce iron briquettes, wherein the hot reduced oxide materials are agglomerated by hot briquetting into larger units (English: hot briqueted iron, short HBI or hot compacted iron, short HCl). Also so-called low-reduced iron (English: low reduced iron, short LRI) can be deducted from the reduction shaft with appropriate process guidance.
    An embodiment of the invention provides that the first partial flow contains only top gas from a reduction reactor of a direct reduction plant. Since this top gas is very nitrogen-rich, the nitrogen can also be well separated in the case of CO 2 deposition by pressure adsorption to obtain a particularly low-nitrogen product gas.
    The steam for the conversion of CO into CO 2 can be produced very economically with waste heat from the plant for the production of pig iron, for example with waste heat from a top gas, an offgas, from the generator gas, from the flue gas of a reduction gas furnace or a raw material drying plant. The waste heat can also come from steelmaking, namely from the converter or the electric arc furnace. Similarly, steam could be used from a power plant where the export gas is burned and used for steam and power generation.
    Part of the water vapor for the conversion of CO into CO 2 can also be generated with the help of a saturator.
    The inventive plant for carrying out the method comprises at least - a plant for pig iron production or a synthesis gas plant, - at least one conversion reactor for the conversion of CO in co2, - a first gas line, with the exhaust gas from the system for
    FOLLOW-UP 2010 26014 11 m * · · »* #« «*»
    • t «·» f t * «1 · I
    · · · · · · «VI I ····· 4 V V |
    Crude iron production or synthesis gas can be passed from the synthesis gas plant in the conversion reactor, - a first C02-deposition plant, which is downstream of the conversion reactor.
    It is characterized in that a second gas conduit for waste gas or synthesis gas is provided, which opens into a second CC > 2 separator system independent of the first, without the waste gas or synthesis gas previously passing through a conversion reactor. For example, the second gas line may branch off from the first before it reaches the conversion reactor. Or it can divide a common gas line for the exhaust gas or synthesis gas into a first and second gas line.
    According to the method variants described above, it can be provided that a line for product gas of a CO 2 separation plant opens into a line for product gas of the other CO 2 separation plant in order to mix the two product gases with one another.
    Furthermore, a line for product gas of the second CO2 separation plant can lead to a direct reduction plant in such a way that the product gas can be used there for carburizing and regulating the carbon content. However, it is not excluded that the mixed product gas of the two CO 2 separation plants is used in this way.
    In particular, a line for product gas of the second CO 2 separation plant can open into a reduction reactor of a direct reduction plant such that the product gas can be introduced into the cooling gas circulation or above the cooling zone, preferably into the transition zone, of the reduction reactor. This embodiment can also be used for mixed product gas.
    ADDENDUM 2010 26014 12: :: :: ,,:: • ·················· I
    The line for residual gas from the second C02 "separation plant can open into a reduction gas furnace of a direct reduction plant and used there as fuel gas.
    In order to mix the two residual gas streams, it may be provided that a line for residual gas of a C02 "separation plant opens into a line for residual gas of the other C02-Äbscheideanlage.
    An embodiment already mentioned in connection with the method presupposes that the first gas line is connected to a direct reduction plant such that the first gas line can be supplied exclusively with top gas from a reduction reactor of a direct reduction plant.
    In the case of using exhaust gases from the
    Pig iron production is provided that the first and / or second gas line are connected to pig iron production facilities such that the gas lines can contain at least one of the following gases: top gas from a blast furnace, in particular from an oxygen blast furnace with top gas recirculation, or a reduction shaft of a smelting reduction plant Exhaust gas from a melter gasifier of a smelting reduction plant, waste gas from at least one fixed bed reactor for preheating and / or reducing iron oxides and / or iron briquettes of a smelting reduction plant (as provided in the FINEX® process), optionally exhaust gas from a CO 2 ~ Separation plant, preferably a PSA plant, which is attributable to the plant for pig iron production (oxygen blast furnace, FINEX®, COREX ©), - exhaust gas from at least one reduction reactor of a direct reduction plant.
    REPLACED 13 2010 26014
    To supply the conversion reactor with steam, it may be provided that a steam line of a heat recovery steam generator of the plant for pig iron production leads into the line before or directly into the conversion reactor, or that a saturator, which cools the exhaust gas or synthesis gas, is arranged in front of the conversion reactor.
    In addition to the already known advantages of a conversion of CO into CO2 such as that - the reduction reactors (blast furnace,
    Fluidized bed reactors, reduction wells) can be made smaller, because the reducing gas is better utilized by the high hydrogen content and has a lower density, - increasing the yield of a (V) PSA plant by 5-10% (H2 + CO) or achievement can be achieved in a same yield as with a VPSA plant, if a PSA plant is used with conversion reactor, in which case the vacuum pumps can be saved, - reducing the risk of so-called "Metal Dusting". Corrosion due to the larger H2 / CO ratio is made possible, the following advantages can be achieved with the method according to the invention: The use of synthesis gas as reducing gas can increase the productivity in the production of DRI / LRI / HCl / HBI in a direct reduction reactor be increased or • a higher metallization and / or carbon content in the direct reduction reactor is possible due to the addition of product gas to the cooling zone of the direct reduction reactor. With the same proportion of oxidants in the reducing gas, a higher reduction gas temperature is possible. Submitted 14 2010 26014
    The H2 / CO ratio of the product gas used as the reducing gas can be adjusted. • Separation of a large part of the nitrogen with (V.sub.2)....... PSA possible by more selective operation of the (V) PSA after CO conversion when recycle gas is converted from direct reduction. Temperature in the reduction zone can be adjusted by adjusting the H2 / C0 ratio and thus adjusting the ratio of predominantly endothermic H2 reduction reactions the predominantly exothermic CO reduction reactions.
    BRIEF DESCRIPTION OF THE FIGURES
    The invention is explained in more detail below with reference to the exemplary and schematic figures.
    1 shows a first embodiment according to the invention of a conversion reactor with two CO 2 deposition plants,
    Fig. 2 shows an arrangement for a conversion reactor and a saturator,
    3 shows a plant according to the invention according to the first embodiment comprising a COREX © plant and a direct reduction plant,
    4 shows a second embodiment of a conversion reactor according to the invention with two CO 2 deposition plants.
    WAYS FOR CARRYING OUT THE INVENTION
    FIG. 1 shows a conversion reactor 1 with two CO 2 separation plants 8, 9 in a first embodiment. Export gas 4, in the form of exhaust from the
    FOLLOWED 15 2010 26014
    Pig iron production, and / or synthesis gas, is compressed with an export gas compressor 13, in one or - shown in dashed lines - several stages. After the export gas compressor 13, a first substream 51 is led to its heating by a heat exchanger 15 and after addition of low-pressure steam 10 shortly before or in the conversion reactor 1 fed to this. The thus modified and heated by the chemical reaction export gas is passed as heat transfer medium again through the heat exchanger 15 and thereby cooled by fresh export gas from the first partial stream 51. Further cooling takes place in a cooler 16 before it enters the first CO 2 separation plant 8.
    A second substream 52 is branched off from the export gas 4 after the export gas compressor 13, but before the heat exchanger 15, and is only supplied via a cooler 14 -not by way of a conversion reactor-to the second CO 2 separation plant 9. The product gas 34 of this second CO 2 separation plant 9 can be supplied wholly or partly to the cooling zone of a reduction shaft 18 of a direct reduction plant 33 or mixed wholly or partially with the product gas 31 and fed to the reduction gas furnace 43 as fuel. The residual gas 12 passes as fuel gas into the reduction gas furnace 43 of the direct reduction plant 33, see FIG. 3.
    The product gas 31 from the first CO 2 separation plant 8 is supplied in its entirety as a reducing gas to the reduction gas furnace 43 for heating it. The residual gas 11 from the first CO 2 separation plant 8 is completely added to the remaining export gas in the export gas container 5, which is no longer returned to the direct reduction plant 33 or the plant for pig iron production, but is mostly used for drying raw materials in the steelworks.
    SUBSCRIBED 16 2010 26014
    The individual process gases have the following properties after a COREXO plant and two plants for pressure swing adsorption (PSA plants):
    Geis 1 Temp. H2 CO C02 <° C) (vol%) {vol%) (vol%) Partial flow 51 before 100-200 30 36 23 Heat exchanger 15 Product gas 31 40 81 5 3 Residual gas 11 40 12 2 82 Product gas 34 40 42 45 1 residual gas 12 40 10 21 59
    By mixing the two product gases 31, 34, the desired CO content can now be set for the subsequent use of the product gases as a reducing gas. For a reduction shaft 18 of a direct reduction plant 33, the ratio H2 / C0 should be between 1.5 and 4.5, since a productivity optimum can be achieved there. But it is also the pressure loss on the reduction shaft or other reduction unit to consider. If the ratio H 2 / CO is too low, due to the excessively high pressure loss via the reduction shaft 18, according to FIG. 3, the system output is reduced due to the hydraulic limitation. If the ratio H2 / CO is too high, then the Möller in the reduction shaft cools down too much due to the predominantly endothermic reactions.
    The export gas 4 can - immediately before the export gas compressor 13, - immediately after this, but before the division of the export gas into two streams 51, 52, and / or - after branching of the second partial stream 52 to the second C02-Abscheideanlage 9, but before the heat exchanger 15, so-called recycle gas 17 are mixed. Recirculation gas 17 is purified top gas 46 from a reduction shaft 18 of a direct reduction plant 33, which partially as
    REPRODUCED 2010 26014
    17
    Fuel gas for the reduction gas furnace 43 of the
    Direct reduction plant 33 is returned, see Fig. 3rd
    In Fig. 2, the system part to the conversion reactor 1 of Fig. 1 is explained in more detail, the branch of the second partial flow 52 or the addition of recycle gas 17 are not shown. The export gas 4 is compressed in the export gas compressor 13 and then has a temperature of 100-200 ° C. It enters a saturator 35, where the export gas 4 preheated water is added. By the heat contained in the export gas 4, the water is evaporated, whereby the addition of further steam can be reduced.
    In the line from the saturator 35 to the heat exchanger 15 is still low-pressure steam 10 is added before the export gas 4 is heated in the heat exchanger 15 to about 300-450 ° C. The conversion reactor 1 of FIG. 1 can be designed in several stages and has here approximately a first conversion unit 38 and a second conversion unit 39, between which a gas cooler 40 is located. During the water gas shift reaction, the gas temperature rises by about 100-150 ° C. Alternatively, the conversion reactor 1 or 38, 39 can also be operated isothermally with simultaneous production of steam. The converted export gas is cooled in the heat exchanger 15 and can be further cooled in a further gas cooler 41, the additional water 42 and / or water from the saturator 35, if it is required for the subsequent first CO 2 deposition plant 8. In the gas cooler 41, the water vapor contained in the converted export gas can also be substantially reduced.
    In the CO 2 deposition plants 8, 9, the CO 2 content is reduced to 0.3-10 vol%.
    FIG. 3 shows the connection according to the invention between a plant for smelting reduction (COREX® plant 32) on the one hand and a direct reduction plant 33 on the other hand.
    SUBSCRIBED 18 2010 26014
    The COREX® plant 32 has in this example a reduction shaft 19, which is designed as a fixed bed reactor and is charged with lump, pellets, sinter and additives, see reference numeral 20.
    In countercurrent to the lump etc. 20, the reducing gas 21 is guided. It is introduced in the lower part of the reduction shaft 19 and exits at its upper side as a top gas 22. The heat of the top gas 22 from the reduction shaft 19 can be used in a waste heat boiler 6 for steam generation, the resulting low-pressure steam can be supplied to the conversion reactor 1, see there reference numeral 10. To the waste heat boiler 6, a bypass line is provided so that the top gas 22 without forced cooling can be performed to the waste heat boiler 6. Before entering the waste heat boiler 6, the top gas 22 can be freed of dust in a dust separator or cyclone 2, for example in the form of a hot gas cyclone. The exhaust gas leaving the waste heat boiler 6 is further purified and cooled in a wet scrubber 3 and, according to the invention, fed as export gas 4 as described above to the uranium conversion reactor 1 for the conversion of CO into CO 2.
    The reducing gas 21 for the reduction shaft 19 is made in a melter gasifier 23, in the one hand coal in the form of lumpy coal or coke 24 and possibly coal in powder form 25 - this O2 -zugeführt together with oxygen, in the other hand, in the Reduction shaft 19 prereduced iron ore is added. The coal in the melter gasifier 23 is gasified, resulting in a gas mixture consisting mainly of CO and H2, and withdrawn as a top gas (generator gas) 26 and a partial flow is fed as a reducing gas 21 to the reduction shaft 19.
    The hot metal melted in the melter gasifier 23 and the slag are withdrawn, see arrow 27.
    The withdrawn from the melter gasifier 23 generator gas 26 is passed after its cooling in a separator 28 (hot gas cyclone) to dust with discharged
    REQUIRED 19 2010 26014
    deposit and return the dust 36 through dust burner in the melter gasifier 23.
    Part of the purified from the coarse dust generator gas 26 is further purified by wet scrubber 37 and removed as excess gas 29 from the COREX® plant 32 and mixed with the export gas 4. Before the wet scrubber 37 and / or in the line for generator gas 26 (not shown), a further waste heat boiler 7 may be arranged, the low-pressure steam is fed to the conversion reactor 1.
    A portion of the purified gas generator 26 after wet scrubber 37 is fed to a cooling gas compressor 30 for cooling and then fed back to the generator gas 26 after the melter gasifier 23 for cooling. As a result of this recycling, the reducing proportions contained therein can still be utilized for the COREX® process and, on the other hand, the required cooling of the hot top or generator gas 26 from approximately 1050 ° C. to 700-900 ° C. can be ensured.
    On the one hand, low-pressure steam 10 from the waste-heat boilers 6, 7 of the COREX © plant 32 can be supplied to the conversion reactor 1 in this exemplary embodiment. Preferably, the waste heat from the iron production process or the direct reduction process should be used because of the short distances between the waste heat boilers 6, 7 and the conversion reactor. 1
    The purified top gas 22 and a portion of the excess gas 29 are withdrawn as export gas 4 from the COREX® plant 32 and compressed before the conversion reactor 1 by means of an export gas compressor 13.
    If an oxygen blast furnace with top gas recirculation is used instead of the COREX® plant 32, the top or blast furnace gas is removed at the top of the blast furnace, a part is returned to the oxygen blast furnace and part of the top or bottom
    REQUIRED 20 2010 26014
    Purified gas pre-cleaned in a dust collector or cyclone and a wet scrubber (or a bag filter or hot gas filter system) cleaned again. The thus purified top or blast furnace gas is then removed directly as export gas 4 from the blast furnace system and at least partially fed to the conversion reactor 1.
    If instead of the COREX® plant 32 a FINEX © plant is used, after the last of the three to four fluidized bed reactors in which the prereduction of the fine ore takes place, a partial stream of the top gas is withdrawn as export gas, cleaned of dust and fed to the conversion reactor 1 , As with the COREX © plant 32, part of the excess gas from the melter gasifier can also be added to the export gas.
    The product gas 31 freed from CO 2 in the first CO 2 deposition plant 8, which is arranged in the substream 51 and designed as a PSA plant, is then heated in a reduction gas furnace 43, which preferably has an air preheater 44. The air preheater 44 provides preheated combustion air 53. The reducing gas furnace 43 can also be supplied with non-preheated air 54 for combustion. The exhaust gas from the reduction gas furnace 43 discharges part of its energy into the combustion air 53 in the air preheater 44 and is then discharged into the atmosphere.
    The product gas 31 is optionally partially oxidized in the reduction gas furnace 43 with oxygen O 2 and then passed into the reduction shaft 18 of the direct reduction plant 33, where the lumpy ore and / or the pellets 45 charged from above are charged.
    The top gas 46 is then further purified in a wet scrubber 49, compressed in a recycle gas compressor 50, before a portion of the export gas 4 is mixed in front of the conversion reactor 1. But a part can also be
    REPLACED 21 2010 26014 are fed via an export gas container 5 to the steam boiler of a steam generating plant as fuel or used for drying raw materials (coal, fine coal or ore drying). Another part is branched off before the recycle gas compressor 50 and used as fuel gas for the reduction gas furnace 43.
    The residual gas 11 from the first CC &gt; 2 precipitator 8 is supplied to the export gas container 13. The residual gas 12 from the second CO 2 separation plant 9, which is preferably designed as a PSA plant, is supplied here in its entirety as fuel gas to the reduction gas furnace 43.
    The product gas 34 from the second CO 2 separation plant 9 can be partially fed to the cooling zone of the reduction shaft 18 of the direct reduction plant 33, in some cases it can be added to the product gas 31 of the first CO 2 separation plant 8. The lower, tapered part of the reduction shaft 18 is the cooling zone, the cylindrical upper part is the actual reduction zone. Between cooling and reduction zone is the transition zone.
    The reduction shaft 18 does not have to be a fixed bed, it can also be designed as a fluidized bed. At the lower end, depending on the charged feedstock and the process, either sponge iron (DRI), hot briquetted iron (HBI), hot compacted iron (HCl) or low reduced iron (LRI low reduced iron) are extracted, see Reference numeral 47. In the case of a fluidized bed, briquetting of the reduced, hot oxide materials is required.
    A portion of the product gases 31, 34 can also be fed to the melter gasifier 23 as a reduction gas, for which purpose it may however have to be previously compressed in a product gas compressor 55. It can then be introduced together with the coal in powder form 25, wherein the product gas serves as a conveying medium for the coal in powder form. Another part 48 of the
    SUBSIDIARY 22 2010 26014 • * * * «» I ι '· «·« «··» * »*« ·· ··· * ·· »t» · * 4 J * * ι * »··» ψ *
    Product gases 31, 34 can be branched off after the product gas compressor 55 and upstream of the melter gasifier 23 and used as a nitrogen substitute in the smelting works, specifically where nitrogen introduction into the process gases is undesirable, for example for cooling coal charging units in the melter gasifier.
    If the exhaust gas from a plant for the production of pig iron is only dedusted dry, e.g. Through ceramic filters or via bag filters, the heat of the exhaust gas for the water gas shift reaction in the conversion reactor 1 can be used. In this case, the compression takes place only after the conversion reactor 1. So if you omit in Fig. 3, the wet scrubber 3 and / or 37, then the export gas compressor 13 in the first part of stream 51 after the conversion reactor 1 and before the first CCh deposition 8 be another compressor in the second partial flow 52 in front of the second CCh deposition system. 9
    FIG. 4 shows a variant embodiment in which only at least partially the recirculation gas of the reduction reactor of a direct reduction plant, that is to say a part of the purified top gas 46 of the reduction shaft 18 from FIG. 3 as recirculation gas 17, is conducted to the conversion reactor 1. Exhaust gas (e.g., export gas 4) of a smelting reduction plant or a blast furnace or synthesis gas is not sent to the conversion reactor 1, but only supplied to the second CO 2 separation plant 9.
    The recycle gas 17 is compressed in a recycle gas compressor 50 and at least partially passed through the heat exchanger 15 to heat it. Another part is passed around the heat exchanger 15 to control the amount that is subjected to CO conversion (partial flow shift). The heated in the heat exchanger 15 recirculated gas passes after the addition of water and / or steam, such as low-pressure steam 10, in the conversion reactor 1 and is a part of its heat in the heat exchanger 15 back to the fresh recycle gas 17 from.
    FOLLOW-UP 23 2010 26014 ft · * · • »* • · · #« * • · t · · · * · I ι
    Another part of the heat is removed in the cooler 16, in front of which also leads around the heat exchanger 15 guided around recirculation gas.
    The recycle gas 17 has a higher nitrogen content by internal enrichment (addition of N2 in the reduction unit, gas recycling) than the other process gas streams, ie first and second part stream 51, 52 of FIG. 1 or the export gas 4 from he smelting reduction or the synthesis gas from a coal gasification. It is known that the adsorption forces occurring during pressure swing adsorption are different for different gases. Thus, they are stronger for water than for CO 2, for CO 2 stronger than for CO and for CO stronger than for nitrogen. For hydrogen they are even lower than for nitrogen. If the first CO 2 separation plant S is designed as a (vacuum) pressure swing adsorption plant and operated in such a way that the nitrogen is also separated, then a very low-nitrogen product gas can be produced without the hydrogen being removed from the product gas.
    The export gas 4 is, as in FIG. 1, compressed only in an export gas compressor 13, cooled in a cooler 14 and then fed to the second CO 2 separation plant 9. The use of the product gases 31, 34 and the residual gases 11, 12 is basically the same as that in FIG. 1.
    LIST OF REFERENCES: 1 conversion reactor 2 dust collector or cyclone 3 wet scrubber 4 export gas 5 export gas container 6 waste heat boiler for top gas 22 7 aftercooler 8 first CO 2 separation plant
    PUBLIC RELEASE 24 2010 26014 ♦ * · * * «« ♦ · * · * · «
    11 Secondary CO 2 separator 10 Low pressure steam 11 Rest gas after first CO 2 separator 8 12 Rest gas after second CO 2 separator 9 13 Export gas compressor 14 Cooler before second CO 2 separator 9 15 Heat exchanger 16 Cooler in front of first CCk separator 17 Recycle gas 18 Reduction shaft of the direct reduction plant 33 19 Reduction shaft of the COREX © plant 32 20 Lumps, pellets, sinters and additives 21 Reduction gas 22 Top gas from reduction shaft 19 23 Melt carburetor 24 Charcoal or coke 25 Coal in powder form 26 Top or generator gas from melter gasifier 23 27 Hot metal and slag 28 Fine ore separator 29 Excess gas 30 Cooling gas compressor 31 Gas released from C02 (product gas) from first C02 separator 8 32 COREX @ plant 33 Direct reduction plant 34 Gas released from C02 (product gas) from second C02 precipitation plant 9 35 Saturator 36 Dust off Separator 28 37 Wet scrubber for Topgas 26 38 first conversion unit 3 9 second conversion unit 40 gas cooler 41 gas cooler 42 additional water, possibly treated water 43 reduction gas furnace 44 air preheater
    REQUIRED 25 2010 26014
    45 Lump ore and / or pellets 46 Topgas from reduction shaft 18 47 Hot briquetted iron or low reduced iron 48 Product gases as nitrogen substitute 49 Wet scrubber for Topgas 46 50 Return gas compressor 51 First partial flow of the exhaust gas or synthesis gas 52 Second partial flow of the exhaust gas or synthesis gas 53 Preheated combustion air 54 Air 55 Product gas compressor
    submitted
    权利要求:
    Claims (20)
    [1]
    26 2010 26014

    1. A process for the treatment of exhaust gases (4) from plants (32, 33) for pig iron production and / or synthesis gas 5, wherein a first substream (51) of the exhaust gas or synthesis gas after addition of water and / or water vapor (10) of a is subjected to at least partial conversion of CO into CO 2 and the exhaust gas or synthesis gas (4) is subsequently subjected to C02-10 deposition, characterized in that a further substream (52) of the exhaust gas or synthesis gas is not subjected to conversion of CO into CO 2, but instead is subjected to a C02 deposition separately from the first partial flow (51).
    [2]
    2. The method according to claim 1, characterized in that the product gases (31, 34) after the respective CO 2 deposition in the first and second part stream (51, 52) for adjusting a certain ratio 20 of hydrogen to CO are mixed together.
    [3]
    3. The method according to claim 1 or 2, characterized in that the product gas (34) is used after the CO 2 deposition in the second partial stream (52) for carburizing and controlling the carbon content in the aftermarket 2010 26014 product of a direct reduction plant (33).
    [4]
    4. The method according to claim 3, characterized in that the product gas {34) is introduced into the cooling gas cycle or 5 above the cooling zone, preferably in the transition zone of the reduction reactor (18).
    [5]
    5. The method according to any one of claims 1 to 4, characterized in that the residual gas {12) after the CO 2 -10 deposition in the second partial flow {52) for combustion, such as in the reduction gas furnace (43) of a direct reduction plant (33) is used.
    [6]
    6. The method according to any one of claims 1 to 5, characterized in that the residual gas (11) after the CO2-15 deposition in the first partial flow (51) and the residual gas (12) after the C02 ~ deposition in the second partial flow (52) with each other be mixed.
    [7]
    7. The method according to any one of claims 1 to 6, characterized in that the exhaust gas (4) contains at least one of the following 20 gases: - top gas from a blast furnace, in particular from an oxygen blast furnace with Topgasrückführung, or a reduction shaft (19) of a smelting reduction plant REPLACED (32), 28 2010 26014 - · Exhaust (29) from a melter gasifier (23) of a smelting reduction plant, - exhaust gas from at least one fluidized bed reactor, - exhaust gas from at least one fixed bed reactor for preheating and / or reduction of iron oxides and / or iron briquettes of a smelting reduction plant, - waste gas from a CO 2 deposition plant assigned to the plant for pig iron production, 10 - waste gas from at least one reduction reactor (18) of a direct reduction plant (33).
    [8]
    8. The method according to any one of claims 1 to 6, characterized in that the first partial flow (51) exclusively top gas (46) from a reduction reactor (18) of a direct reduction plant 15 (33).
    [9]
    9. The method according to any one of claims 1 to 7, characterized in that a portion of the steam for the conversion of CO in CO 2 is produced with waste heat of the plant for pig iron production (32).
    [10]
    10. The method according to any one of claims 1 to 7, characterized in that a part of the steam for the conversion of CO into CO 2 is made with waste heat of the exhaust gas or synthesis gas (4) itself. REPLACED 29 2010 26014


    [11]
    11. Plant for carrying out the method according to one of claims 1 to 10, comprising at least - a plant (32) for pig iron production and / or a synthesis gas plant, 5 - at least one conversion reactor (1) for the conversion of CO into CO 2, - a first gas line , with the exhaust gas (4) from the plant for pig iron production or synthesis gas from the synthesis gas plant in the conversion reactor (1) 10 can be passed, - a first CO 2 deposition plant (8), which the conversion reactor (1), characterized in that a second gas line is provided for waste gas or synthesis gas, which in 15 opens a second CO 2 separation plant (9) independent of the first, without the waste gas or synthesis gas previously passing through a conversion reactor.
    [12]
    12. Plant according to claim 11, characterized in that a line for product gas (31) of a CO 2 separation plant (8) opens into a line for product gas (34) of the other CO 2 separation plant (9).
    [13]
    13. Plant according to claim 11 or 12, characterized in that a line for product gas (34) 30 30 26014 of the second CO 2 separation plant (9) so in a direct reduction plant (33) opens, that the product gas (34) there for carburizing and regulation of the carbon content.
    [14]
    14. Plant according to one of claims 11 to 13, characterized in that a line for product gas (34) of the second CO 2 separation plant (9) so in a reduction reactor (18) of a direct reduction plant (33) opens, that the product gas (34) can be introduced into the cooling gas circulation or above the cooling zone, preferably into the transition zone, of the reduction reactor.
    [15]
    15. Plant according to one of claims 11 to 14, characterized in that a line for residual gas (12) 15 from the second CC> 2-deposition plant (9) in a reduction gas furnace (43) of a direct reduction plant (33) opens.
    [16]
    16. Plant according to one of claims 11 to 15, characterized in that a line for residual gas (11) 20 of a CC> 2-Abscheideanlage (8) in a line for residual gas (12) of the other COj-Abscheideanlage (9) opens.
    [17]
    17. Plant according to one of claims 11 to 16, characterized in that the first gas line is so connected with REAGENT 31 2010 26014 a direct reduction plant (33) that the first gas line exclusively with top gas (46) from a reduction reactor (18) of a direct reduction plant can be supplied.
    [18]
    18. Plant according to one of claims 11 to 16, characterized in that the first and / or second gas line are connected to plants (33) for pig iron production, that the gas lines may contain at least one of the following gases: - Topgas from a blast furnace, in particular from an oxygen blast furnace with Topgasrückführung, or a reduction shaft (19) of a smelting reduction plant - exhaust gas from a melter gasifier (23) a smelting reduction plant, - exhaust gas from at least one fluidized bed reactor, - exhaust gas from at least one fixed bed reactor for preheating and / or reduction of iron oxides and / or iron briquettes a smelting reduction plant, waste gas from a CO 2 separation plant assigned to the plant for pig iron production, waste gas from at least one reduction reactor (18) of a direct reduction plant (33).
    [19]
    19. Plant according to one of claims 11 to 18, characterized in that a steam line of a heat recovery steam generator (6, 7) of the plant (32) to the REPLACEMENT 2010 26014 "50 · * · · * *» ··. ································································································································································································································ 5
    [20]
    20. Plant according to one of claims 11 to 19, characterized in that a saturator (35), which cools the exhaust gas or synthesis gas, in front of the conversion reactor (1, 38, 39) is arranged. SUBSEQUENT
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    同族专利:
    公开号 | 公开日
    RU2014112201A|2015-10-10|
    CN103764854A|2014-04-30|
    ZA201401392B|2014-12-23|
    UA111620C2|2016-05-25|
    US9377242B2|2016-06-28|
    RU2618971C2|2017-05-11|
    KR20140066211A|2014-05-30|
    CN103764854B|2015-08-19|
    AU2012301152A1|2014-02-27|
    US20140202285A1|2014-07-24|
    WO2013030057A1|2013-03-07|
    AT511892B1|2013-07-15|
    CA2846689A1|2013-03-07|
    EP2751294B1|2017-08-02|
    EP2751294A1|2014-07-09|
    KR101961418B1|2019-03-22|
    BR112014004521A2|2017-03-28|
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    法律状态:
    2016-06-15| PC| Change of the owner|Owner name: PRIMETALS TECHNOLOGIES AUSTRIA GMBH, AT Effective date: 20160415 |
    2020-04-15| MM01| Lapse because of not paying annual fees|Effective date: 20190831 |
    优先权:
    申请号 | 申请日 | 专利标题
    ATA1245/2011A|AT511892B1|2011-08-31|2011-08-31|METHOD FOR THE TREATMENT OF EXHAUST GASES FROM PLANTS FOR THE PRODUCTION OF RAW CHEMISTRY AND / OR SYNTHESEGAS|ATA1245/2011A| AT511892B1|2011-08-31|2011-08-31|METHOD FOR THE TREATMENT OF EXHAUST GASES FROM PLANTS FOR THE PRODUCTION OF RAW CHEMISTRY AND / OR SYNTHESEGAS|
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    KR1020147008568A| KR101961418B1|2011-08-31|2012-08-22|Method for treating waste gases from plants for pig iron production and/or synthesis gas|
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    US14/240,430| US9377242B2|2011-08-31|2012-08-22|Method for treating waste gases from plants for pig iron production|
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