• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    1460852 Reduction of metal oxides SVENSKA KULLAGERFABRIKEN AB 25 Jan 1974 [26 Jan 1973] 03481/74 Heading C7D Metal is extracted from oxides by a process which includes blowing pre-reduced oxide material in a carrier gas into the lower part of a furnace containing a stack of solid reductant, the temperature of that part of the stack being at or above the melting point of the metal. In a preferred embodiment, coke 5 is contained in a shaft furnace 4 while oxygen in pipe 8 and hydrocarbon in pipe 7 is blown in though tuyeres 10; alternatively or additionally, the furnace may be heated electrically, e.g. with plasma burners or through graphite electrodes. Pre-reduced oxidic ore is blown through pipe 21 into the bottom of the furnace using inert or reducing carrier gas and final reduction and melting occur simultaneously to provide molten iron 9. Preferably, outgoing gases 12, a mixture of carbon monoxide and hydrogen, are used to prereduce the oxidic material 16 in a fluidized bed 20, and to dry ingoing oxidic material at 17, and may be recycled to an upper part of the furnace at 30. By using these outgoing gases in the pre-reduction step, the process is self-regulating. The method is particularly applicable to iron ores e.g. haemetite, but it may be applied to ores containing tungsten, chromium, manganese, nickel, copper, cobalt or vanadium.
    公开号:SU869562A3
    申请号:SU741994568
    申请日:1974-01-25
    公开日:1981-09-30
    发明作者:Гуннар Пердал Эрн；Оскар Сантен Свен
    申请人:Стифтельзен Фор Металлургиск Форскнинг (Фирма)；
    IPC主号:
    专利说明:

    The invention relates to the direct radiation of metals from ores, in particular to the direct production of iron. The closest in technical essence and the achieved result to the proposed method is the production of iron from ore in a shaft furnace, including preliminary reduction by recirculation gases and subsequent high-temperature treatment with injection of a pre-reduced material or its mixture with slag-forming reagents, transporting inert or reducing gas with 1m The disadvantage of this method is the low intensification of the process, since in this process large demands are made. ovani to strength used as a coke reducing agent. In addition, a shaft furnace requires extensive outdoor equipment, such as for blowing air. The purpose of the invention is to reduce energy costs. This goal is achieved in that the pre-reduced material is blown above the level of the molten metal against a column of solid reducing agent. In the process of the preliminary reducing agent, the gas from the upper part of the reactor, containing mainly a mixture of carbon monoxide and hydrogen, is used as a reducing agent. To achieve a high degree of anticipation, an additional amount of hydrocarbon-containing reducing gas or a specially produced reducing gas can be added to the reactor in order to increase the amount of gas leaving the reactor in order to achieve a high degree of prediction. The proposed method is, to a certain extent, self-regulating in such a way that as the degree of reduction in the precautionary step decreases, the amount of gas released from the reactor automatically increases, causing an increase in the degree of recovery when the specimen is restored, at a constant injection temperature at the injection level. In contrast, when the reduction rate in the anticipation stage is high, the amount of gas produced in the shaft furnace will automatically decrease, causing There is a decrease in the pre-reduction stage, which also takes place at a constant temperature in the lower part of the mine at the injection level.
    The recovery gases taken from the reactor have relatively high temperatures, their temperature is controlled by a heat exchanger to a temperature acceptable for anticipation. Prevention, of course, can be carried out in one or more steps according to known processes, for example in a fluidized bed.
    Energy can be supplied, for example, with the help of oxygen and hydrocarbons, as well as in the form of electrical energy using conventional electrodes or through the installation of a plasma torch. A solid reducing agent, of course, performs, of course, a double function, on the one hand as a reducing agent for direct reduction, and on the other hand as a fuel.
    This method can be used to restore most of the known oxidized ores, such as ores of wolfra, chromium, manganese or nickel, or a mixture of one or more of these ores and / or iron ores, whereby pure metal or alloy can be obtained depending on the material introduced into the reactor.
    The drawing shows schematically an apparatus for carrying out the proposed method.
    As an example, the production of pig iron is taken, but the method can be used, in addition to iron ores, on other oxidized ores.
    The device includes a final reduction stage consisting of a shaft furnace type reactor 1 loaded from above with a solid reducing agent, in this case carbon, for example coke, through a gas-tight gate 2. Pre-reduced oxidized material is blown to the bottom of the reactor through tuyeres 3 with fully inert or reducing gas B At the same time, oxygen and hydrocarbons are injected into the tuyeres 3 through pipelines 4 and 5. The final reduction and melting occur instantaneously and the molten metal, in the two cases the iron n, flows to the bottom while carburizing. Hence, the obtained pig iron and slag can be continuously produced.
    or periodically through the outlet 6. For the metallurgical treatment of the product obtained, the reactor can be equipped with a meta-receiver 7.
    The temperature of the reactor is controlled by oxygen and, possibly.
    water, or also with the help of electrical energy supplied, for example, using a plasma torch resistive with graphite electrodes. One of the phases may be a reactor wall.
    The reactor and the blow-off coke are of hot dimensions such that the injected pre-reducing material is picked up in the lower hot part of the blow-off coke; The gas leaving the reactor contains a mixture of carbon monoxide and hydrogen in high concentration.
    The ratio of CO / Hij is regulated by the addition of hydrocarbons to the bottom, as well as by the height of the blow-off coke in
    5 reactor.
    The hot reducing gas leaving the reactor has a temperature controlled by a heat exchanger 8 to a temperature acceptable for
    0 stages of anticipation. The prediction may be carried out in one or more stages agreed upon in a known manner, for example in a fluidized bed.
    5 An acceptable degree of anticipation for an oxidized material is 60-95%. With a reduction rate above 90%, the reducing gas from the reactor will possibly be
    Q is not sufficient due to the reduction of the heat load in the reactor and the reduced consumption for the final reduction, and therefore gas must be provided from a separate source 9, for example a gas generator.
    The gas leaving the pre-reduction stage 10 still contains a relatively large amount of combustible gases and can therefore be used on the one hand for heating and drying in the dryer 11 of the incoming oxidized material and, on the other hand, in the gas generator or after possible removal of water in the device 12 for re-introduction into
    5, the final reduction reactor is at a slightly higher level through tuyeres 13 than the reaction zone of the reactor, as a result of which the output temperature from the reactor will also be reduced and the need to install an additional heat exchanger 8 will be reduced.
    The oxidized material entering the reactor, in this case iron ore, is preferably fine and may be in the form of ore concentrate or a mixture of concentrate and dust, for example, from other metallurgist processes causing air pollution problems.
    By injecting a single preventive material, a small amount can be successfully used as a carrier gas;
    5 of the reactor gas cleaned in an appropriate purifier with a filter 14 and transmitted by a fan 15. The emissions from the dryer 11 are sent to the stack through pipe 16. Example 1. In this experiment, the input material is coke, oxygen, hematite () and anticipation is carried out to the stage. Gas recirculation from the reactor to the recovery stage is not available. In this experiment, a consumption of 660 kg of coke and 495 nm of oxygen per ton of melted pig iron was obtained. Example2. The injected material is coke, oxygen, hematite and pre-reduction carried out in two stages without recirculation of gas from the reactor. With a two-step anticipation, better use of gas from the reactor is achieved. In this test, a degree of anticipation of 80% and a consumption of 480 kg of coke and 372 nm of oxygen per ton of processed iron were obtained. Prizem, the Material consists of coke, hematite and heat is provided with electrical energy. In this method, very small amounts of gas are obtained and therefore it is possible to achieve a recovery of only 37% by anticipating recovery in two stages. Therefore, it is better to conduct an experiment with a one-step prediction, and a 33% prediction will be obtained. In this experiment, 215 kg of coke and energy consumption of 1200 kWh per ton of fused pig iron were burned. EXAMPLE 4. The input materials are the same as in example 3, but the energy supplied was successfully replaced by oxygen and coke, and at the same time, the restoration was expanded to two stages. In the limiting case, per ton of molten pig iron without any electric power, the same flow rates were achieved as in example 2.. Example5. The injected materials coke, hematite, recirculating gas. In such an amount that it is obtained, a 75% prediction, - the need for heat is covered by electrical energy. About 55% of the gas from the reactor was recycled while the rest of the gas was used to heat or dry the ore concentrate. In this experiment, coke consumption of 215 kg and consumption of electrical energy of 1270 kWh per ton of molten pig iron were achieved. The flow rates are approximately equal, but somewhat less satisfactory than those achieved in Example 3. Measurement 6. Input materials — coke, hematite, filtered recirculating gas from the reactor, and heat are supplied by electrical energy. Coke consumption is 161 kg and electricity consumption is 610 kWh per ton of molten pig iron. , Example.7. In this experiment, the input materials — hydrocarbon, coke, hematite, and heat — are provided with electrical energy. Coke can be replaced either completely or partially with a hydrocarbon, but the reactor should always be on the float; Non-coke to the normal experimental level, on the one hand, to guarantee a strong reducing medium and, on the other hand, to produce a pure reducing gas. In this case, oil is used as a hydrocarbon, but it can also be replaced by other hydrocarbons, even gaseous ones. 180 tons of oil and 1240 kWh of electricity were consumed per ton of molten pig iron. EXAMPLE 8 Input materials are propane, hematite, purified recycle gas, and heat is provided with electricity. All recycled gas is purified and returned to the process. 124 kg of propane (SzNd) and 1125 kWh of electricity were consumed per ton of molten pig iron. The table shows the energy consumption for various processes, corresponding to the proposed method in the production of pig iron. The table includes 8 examples and it is clear from it that the process according to example 3 is the most difficult from the point of view of energy consumption. All the experiments and experiments listed above were carried out in experimental equipment and it is obvious that the true expenditure indices for large-scale production will probably be higher than those given in the table.
    Table continuation
    权利要求:
    Claims (1)
    [1]
    Claim
    The process for producing metal from its oxide comprising prereduction gas-recirculation "L Zami and subsequent processing of the high-temperature hydrochloric m in the shaft furnace by blowing the pre-reduced material, or mixtures thereof with slag forming ro1t * cients, conveying an inert or reducing gas, wherein that, in order to reduce energy costs, pre-reduced material is blown over the level of molten metal against a column of solid reducing agent.
    类似技术:
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    同族专利:
    公开号 | 公开日
    BE885198Q|1980-12-31|
    FR2215478A1|1974-08-23|
    DE2403780B2|1977-05-26|
    JPS49110519A|1974-10-21|
    DE2403780C3|1980-08-14|
    CA1013150A|1977-07-05|
    JPS5720366B2|1982-04-28|
    GB1460852A|1977-01-06|
    DE2403780A1|1974-08-01|
    FR2215478B1|1976-11-26|
    SE388210B|1976-09-27|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    WO2005061739A1|2003-12-22|2005-07-07|Anatoly Timofeevich Neklesa|Device for producing iron from iron-containing raw material|
    MX153453A|1979-07-16|1986-10-16|Mindres Int Bv|IMPROVEMENTS IN METHOD AND APPARATUS FOR THE PRODUCTION OF CAST CAST IRON|
    SE429561B|1980-06-10|1983-09-12|Skf Steel Eng Ab|SET FOR CONTINUOUS PREPARATION OF LOW CARBON CHROMES OF CHROMOXIDE CONTAINING MATERIALS USING A PLASMA MAGAZINE|
    SE444956B|1980-06-10|1986-05-20|Skf Steel Eng Ab|SET OUT OF METAL OXID-CONTAINING MATERIALS EXCAVING INGREDIENT EASY METALS OR CONCENTRATES OF THESE|
    FR2500478B2|1980-07-15|1986-11-14|Siderurgie Fse Inst Rech|PROCESS FOR REDUCING THE CONSUMPTION OF REDUCING AGENTS IN AN APPARATUS FOR REDUCING AND FUSING METAL ORES, ESPECIALLY IN A BLAST STEEL FURNACE|
    SE439932B|1980-11-10|1985-07-08|Skf Steel Eng Ab|PROCEDURE FOR THE MANUFACTURE OF METAL FROM NICE CORNED METAL OXIDE MATERIAL|
    ZA811540B|1981-03-09|1981-11-25|Skf Steel Eng Ab|Method of producing molten metal consisting mainly of manganese and iron|
    DE3273996D1|1981-04-28|1986-12-04|Kawasaki Steel Co|Methods for melting and refining a powdery ore containing metal oxides and apparatuses for melt-refining said ore|
    AU552070B2|1981-10-19|1986-05-22|Council For Mineral Technology|Producing and treating ferro chrome by arc thermal plasma|
    SE500352C2|1982-04-07|1994-06-06|Nordic Distributor Supply Ab|Ways of extracting metals from liquid slag|
    SE436124B|1982-09-08|1984-11-12|Skf Steel Eng Ab|SET TO MAKE PROCESS|
    AT382165B|1983-08-18|1987-01-26|Voest Alpine Ag|METHOD FOR THE PRODUCTION OF LIQUID PIPE IRON OR STEEL PRE-PRODUCTS AND DEVICE FOR IMPLEMENTING THE METHOD|
    DE3438487C2|1984-10-17|1987-10-15|Korf Engineering Gmbh, 4000 Duesseldorf, De|
    SE453304B|1984-10-19|1988-01-25|Skf Steel Eng Ab|KIT FOR MANUFACTURE OF METALS AND / OR GENERATION OF BATTLE FROM OXIDE ORE|
    DE4108283A1|1991-03-14|1992-09-17|Kortec Ag|METHOD FOR PRODUCING LIQUID METAL FROM FINE-GRAIN METAL OXIDE PARTICLES, AND REDUCTION AND MELTING STOVES FOR CARRYING OUT THE METHOD|
    GB9108778D0|1991-04-24|1991-06-12|British Steel Plc|Production of ferromanganese|
    DE19634348A1|1996-08-23|1998-02-26|Arcmet Tech Gmbh|Melting unit with an electric arc furnace|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    SE7301099A|SE388210B|1973-01-26|1973-01-26|MAKE A REDUCTION OF METAL FROM METAL OXIDES|
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