This application is the national phase of, and claims priority to, International Patent Application No. PCT/EP2014/003317, filed Dec. 11, 2014, which designated the U.S. and which claims priority to German Patent Application Number DE 10 2013 113 933.7, filed Dec. 12, 2013. These applications are each incorporated by reference herein in their entireties.
1. Field of the Invention
The invention relates to a method for producing syngas in combined operation with a metallurgical plant which comprises at least one blast furnace for producing crude iron, a converter steel mill and a coke-oven plant.
2. Description of the Related Art
Crude iron is obtained in the blast furnace from iron ores, additives such as coke and other reducing agents such as coal, oil, gas, biomasses, recycled waste plastics or other substances containing carbon and/or hydrogen. CO, CO2, hydrogen and water vapour inevitably occur as products of the reduction reactions. Apart from the aforementioned constituents, a blast-furnace top gas drawn off from the blast-furnace process often has a high content of nitrogen. The amount of gas and the composition of the blast-furnace top gas are dependent on the feedstock and the operating mode and are subject to fluctuations. Typically, however, blast-furnace top gas contains 35 to 60% by volume N2, 20 to 30% by volume CO, 20 to 30% by volume CO2 and 2 to 15% by volume H2. Around 30 to 40% of the blast-furnace top gas produced in the production of the crude iron is generally used for heating up the hot air for the blast-furnace process in air heaters; the remaining amount of top gas may be used in other areas of the mill for heating purposes or for electricity generation.
In the converter steel mill, which is arranged downstream of the blast-furnace process, crude iron is converted into crude steel. By blowing oxygen onto liquid crude iron, troublesome impurities such as carbon, silicon, sulphur and phosphorus are removed. Since the oxidation processes cause an intense development of heat, scrap is often added in amounts of up to 25% with respect to the crude iron as a coolant. Furthermore, lime is added for forming slag and an alloying agent. A converter gas that has a high content of CO and also contains nitrogen, hydrogen and CO2 is drawn off from the steel converter. A typical converter gas composition has 50 to 70% by volume CO, about 10 to 20% by volume N2, about 15% by volume CO2 and about 2% by volume H2. The converter gas is either burned off or, in the case of modern steel mills, captured and passed on to be used for providing energy.
In the coke-oven plant, coal is converted into coke by a coking process. A coke-oven gas thereby occurs, containing a high hydrogen content and considerable amounts of CH4. Typically, coke-oven gas contains 55 to 70% by volume H2, 20 to 30% by volume CH4, about 5 to 10% by volume N2 and about 5% by volume CO. In addition, the coke-oven gas has fractions of CO2, NH3 and H2S. In practice, the coke-oven gas is used in various areas of the works for heating purposes and in the power-generating process for electricity generation. In addition, it is known to use coke-oven gas together with blast-furnace top gas or with converter gas for producing syngases. According to a method known from WO 2010/136313 A1, coke-oven gas is separated into a hydrogen-rich gas stream and a residual gas stream containing CH4 and CO, the residual gas stream being fed to the blast-furnace process and the hydrogen-rich gas stream being mixed with blast-furnace top gas and processed further into a syngas. It is known from EP 0 200 880 A2 to mix converter gas and coke-oven gas and use them as a syngas for methanol synthesis.
In an integrated metallurgical plant that is operated in combination with a coking plant, approximately 40 to 50% of the raw gases that occur as blast-furnace top gas, converter gas and coke-oven gas are used for chemical engineering processes. Approximately 50 to 60% of the gases produced can be used for electricity generation or used as raw gases for producing syngas. By using the gases for producing syngas, the cost-effectiveness of a metallurgical plant can be improved. At the same time, the CO2 balance of the metallurgical plant also improves, since carbon is bound in chemical products and is not emitted in the form of CO2. However, it must be taken into consideration here that the amount of raw gas that can be used for producing syngas is subject to considerable fluctuations over time.
This is so because, as long as the raw gases are used for producing syngas, the production of electricity by a power-generating plant operated in combination with the metallurgical plant must be cut back and electricity obtained from external sources to cover the electricity demand of the metallurgical plant. If electricity is available at low cost and in sufficient amounts, for example from renewable energy sources, a great amount of raw gas can be used for producing syngas. On the other hand, when there is a high price for the externally obtained electricity, it is necessary from economic considerations to use the usable amount of raw gas that occurs in the metallurgical plant at least predominantly for electricity generation and to cut back the production of syngas.
One object of the invention includes providing a method for producing syngas in combined operation with a metallurgical plant with which it is possible to use the raw gases that occur in varying amounts and varying composition in a metallurgical plant as completely as possible in cost-effective processes.
According to the invention, part of the blast-furnace top gas that is produced in the production of crude iron and/or part of the converter gas that occurs in the converter steel mill and/or part of the coke-oven gas that is produced in the coke-oven plant are mixed. By choosing the gas streams that are brought together to form a mixed gas and/or by changing the mixing ratios of the gas streams that are brought together, two or more streams of useful gas are thereby produced, differing with regard to their composition and respectively prepared to form streams of syngas.
The preparation of the streams of useful gas comprises in particular a gas-cleaning operation and a gas-conditioning operation. A steam-reforming operation with water vapour, a partial oxidation with air or oxygen and a water-gas-shift reaction for the conversion of a CO fraction may be used for example for the gas conditioning. The conditioning steps may be used individually or else in combination.
The streams of syngas produced by the method according to the invention are gas mixtures that are used for synthesis. The term “syngas” covers for example mixtures of N2 and H2 for ammonia synthesis and in particular gas mixtures that mainly contain CO and H2 or CO2 and H2 or CO, CO2 and H2. From the syngases, chemical products that respectively contain the components of the reactant can be produced in a chemical plant. Chemical products may be for example ammonia or methanol or else other hydrocarbon compounds.
For producing ammonia, a syngas that contains nitrogen and hydrogen in the correct ratio must be provided. The nitrogen can be obtained from blast-furnace top gas. Blast-furnace top gas or converter gas may be used in particular as the hydrogen source, hydrogen being produced by conversion of the CO fraction by a water-gas-shift reaction (CO+H2OCO2+H2). A mixture of coke-oven gas and blast-furnace top gas or a mixed gas comprising coke-oven gas, converter gas and blast-furnace top gas may also be used for producing a syngas for ammonia synthesis. For producing hydrocarbon compounds, for example methanol, it is necessary to provide a syngas consisting substantially of CO and/or CO2 and H2 that contains the components carbon monoxide and/or carbon dioxide and hydrogen in the correct ratio. The ratio is often described by the module (H2−CO2)/(CO+CO2). The hydrogen may be produced for example by conversion of the CO fraction in the blast-furnace top gas by a water-gas-shift reaction. Converter gas may be used for providing CO. Blast-furnace top gas and/or converter gas may serve as a source of CO2. A mixed gas comprising coke-oven gas and converter gas or a mixed gas comprising coke-oven gas, converter gas and blast-furnace top gas is also suitable for producing hydrocarbon compounds.
Within the scope of the invention, a biotechnological plant may also be used instead of a chemical plant for producing chemical products from syngas. The plant concerned is a plant for the fermentation of syngas. Syngas should be understood in this case as including mixtures of CO and H2 with which alcohols, acetone or organic acids can be produced. However, when a biochemical process is used, the hydrogen originates substantially from the water that is used as a medium in the fermentation. Converter gas is preferably used as a source for CO. The use of blast-furnace top gas or a mixed gas comprising converter gas and blast-furnace top gas is likewise possible. By contrast, the use of coke-oven gas is unfavourable for a biotechnological process. Consequently, products that contain carbon from the CO fraction of the raw gases that occur in a metallurgical plant and hydrogen from the water used in a fermentation process can be produced by means of a biotechnological process.
With the method according to the invention, raw gases that occur in a metallurgical plant in the production of crude iron, in the production of crude steel and in the production of coke can be used to produce at the same time streams of syngas, which are used in a chemical plant and in a biotechnological plant operated in parallel therewith for producing chemical products. The chemical plant and the biotechnological plant are arranged in parallel and can be operated at the same time or else in alternation. This makes it possible for the metallurgical plant to be operated in a cost-effective way, in particular even when the amounts of gas that can be used for producing syngas are subject to daily fluctuations.
An advantageous refinement of the method according to the invention provides that a first stream of useful gas, containing H2, is formed and by gas conditioning is turned into a first syngas, which contains for example CO and H2 or N2 and H2 as the main constituents, and that a second stream of useful gas, which is substantially free from H2 and contains CO as the main constituent, is produced. The second stream of useful gas may consist in particular of converter gas or blast-furnace top gas or a mixed gas formed from converter gas and blast-furnace top gas.
A further variant of an embodiment of the invention provides that a first stream of useful gas is formed by mixing at least two gas streams that occur as blast-furnace top gas, converter gas or coke-oven gas, and that a second stream of useful gas consists only of blast-furnace top gas, converter gas or coke-oven gas.
The coke-oven gas and/or the blast-furnace top gas is expediently already cleaned before being used as useful gas, the cleaning having the effect of removing inter alia carbon black, high-boiling hydrocarbons, aromatic hydrocarbons (BTX), sulphur and sulphur compounds. In this case, the streams of useful gas are expediently cleaned before a gas-conditioning operation.
A further refinement of the invention provides that the hydrogen content of at least one stream of useful gas is set by separating out hydrogen, for example by means of a pressure swing adsorption plant, or by enriching with hydrogen. The hydrogen necessary for enriching may be produced in the metallurgical plant, for example by electrolysis of water. Furthermore, the hydrogen content of at least one stream of useful gas may be set by converting CO in a water-gas-shift reaction or by reforming CH4.
The invention is explained below with respect to
The plant complex represented in
Crude iron is obtained in the blast furnace 2 substantially from iron ore and reducing agents, in particular coke and coal, oil, gas, biomasses and recycled plastics or other compounds containing carbon and/or hydrogen. A reduction reaction causes the production of a blast-furnace top gas 6, which contains as the main constituent nitrogen, CO, CO2 and a small proportion of H2. In the converter steel mill 3, which is arranged downstream of the blast-furnace process, crude iron is converted into steel. By blowing oxygen onto the liquid crude iron, troublesome impurities, in particular carbon, silicon and phosphorus, are removed. At the top of the converter, a converter gas 7 that has a high proportion of CO is drawn off. The metallurgical plant 1 also comprises a coke-oven plant 4. In the coking of coal into coke, coke-oven gas 8 occurs, containing a high proportion of hydrogen and CH4.
According to an overall balance represented in
According to the plant diagram represented in
In the exemplary embodiment, a first stream of useful gas 13, containing H2, is formed and by gas conditioning is turned into a first syngas 13′, which contains for example CO and H2 or N2 and H2 as the main constituents. In a chemical plant 15, the syngas 13′ is used for the synthesis of chemical products, for example ammonia, methanol or other hydrocarbon compounds. Furthermore, a second stream of useful gas 14, which is substantially free from H2 and contains CO as the main constituent, is produced. The second stream of useful gas 14 consists of converter gas 7 or blast-furnace top gas 6 or a mixed gas formed from converter gas 7 and blast-furnace top gas 6. In a biotechnological plant 16, products that contain carbon from the CO fraction of the gases mentioned and hydrogen are produced. The hydrogen in this case originates substantially from the water that is used as a medium in the fermentation. The chemical plant 15 and the biotechnological plant 16 may be operated in parallel or else alternately. In the exemplary embodiment, they are arranged in parallel with a power-generating plant 17, which is designed as a gas-turbine power-generating plant or gas-turbine and steam-turbine power-generating plant and is operated with coke-oven gas 8, blast-furnace top gas 6 or converter gas 7 or a mixed gas composed of these gas components. Externally obtained electricity and power-generating plant electricity, which is produced by the power-generating plant 17 of the plant complex, are used to cover the electricity demand of the plant complex. To achieve operation of the plant complex that is as cost-effective as possible, at times of low electricity prices electricity is bought in and the operation of the power-generating plant 17 is cut back. Correspondingly, a great stream of raw gas can be used for producing syngas. If external electricity, for example from renewable energy sources, is not available to a sufficient extent and at acceptable prices, the production of syngas is reduced and the raw gas 6, 7, 8 is used more in the power-generating plant 17 for electricity generation.
Number | Date | Country | Kind |
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10 2013 113 933 | Dec 2013 | DE | national |
Filing Document | Filing Date | Country | Kind |
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PCT/EP2014/003317 | 12/11/2014 | WO | 00 |
Publishing Document | Publishing Date | Country | Kind |
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WO2015/086151 | 6/18/2015 | WO | A |
Number | Name | Date | Kind |
---|---|---|---|
3595619 | Slater et al. | Jul 1971 | A |
3767379 | Marion | Oct 1973 | A |
5454853 | Edelson | Oct 1995 | A |
20060027043 | Zendejas-Martinez | Feb 2006 | A1 |
20100294312 | Richter | Nov 2010 | A1 |
20140343339 | Schodel | Nov 2014 | A1 |
20150299594 | Hinnemann | Oct 2015 | A1 |
20160348196 | Achatz et al. | Dec 2016 | A1 |
Number | Date | Country |
---|---|---|
1803746 | Jul 2006 | CN |
101343580 | Jan 2009 | CN |
102211977 | Oct 2011 | CN |
103525965 | Jan 2014 | CN |
3101067 | Jul 1982 | DE |
102011077819 | Dec 2012 | DE |
102011113547 | Mar 2013 | DE |
102013113913 | Jun 2015 | DE |
102013113921 | Jun 2015 | DE |
102013113942 | Jun 2015 | DE |
102013113950 | Jun 2015 | DE |
102013113958 | Jun 2015 | DE |
102013113980 | Jun 2015 | DE |
0200880 | Nov 1986 | EP |
200880 | Nov 1986 | EP |
244551 | Mar 1990 | EP |
2543743 | Jan 2013 | EP |
2657215 | Oct 2013 | EP |
2420568 | Oct 1979 | FR |
H02254115 | Jan 1990 | JP |
2011225969 | Nov 2011 | JP |
20130075031 | Jul 2013 | KR |
2353036 | Apr 2009 | RU |
0005421 | Feb 2000 | WO |
2010136313 | Dec 2010 | WO |
2011018124 | Feb 2011 | WO |
2015086148 | Jun 2015 | WO |
2015086149 | Jun 2015 | WO |
2015086150 | Jun 2015 | WO |
2015086151 | Jun 2015 | WO |
2015086152 | Jun 2015 | WO |
2015086153 | Jun 2015 | WO |
2015086154 | Jun 2015 | WO |
Entry |
---|
EP-0200880-A2 machine translation (Year: 1986). |
CN 103525965 machine translation (Year: 2014). |
JP H02254115 machine translation (Year: 1990). |
KR 20130075031 A machine translation (Year: 2013). |
CN 102211977 A machine translation (Year: 2011). |
DE 3101067 machine translation (Year: 1982). |
JP H02-254115 human translation (Year: 1990). |
ESPACNET family data for publications including US 2014343339 (Year: 2014). |
EP 0200880 A1 human translation (Year: 1986). |
Chinese Application No. 201480067680.7, Office Action dated Apr. 6, 2017, 21 pages. |
PCT Application No. PCT/EP2014/03317, Written Opinion, dated Jun. 18, 2015, 10 pages. |
PCT Application No. PCT/EP2014/03317, International Search Report, dated Jun. 18, 2015, 5 pages. |
Canadian Application No. 2,930,463, Office Action dated Mar. 27, 2017, 6 pages. |
EP 308037 A1 (using English translation of Abstract of corresponding published application DE 102013113933), published Jun. 18, 2015. |
Russian Application No. 2016127975, Office action dated Dec. 19, 2017, 11 pages |
Canadian Application No. 2,930,463, Office Action dated Oct. 18, 2017, 3 pages. |
Number | Date | Country | |
---|---|---|---|
20160348196 A1 | Dec 2016 | US |