• 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:
    A method and apparatus for the direct reduction of iron oxide utilizing sulfur-containing gas such as coke oven gas for the process gas. Sulfur-containing gas is heated and injected above the reduction zone to transfer the sulfur to the hot burden. The apparatus includes an upper bustle zone for prereduction and sulfur transfer and a lower bustle zone for the final reduction of the burden to metallized iron.
    公开号:SU978735A3
    申请号:SU802996898
    申请日:1980-10-21
    公开日:1982-11-30
    发明作者:Артур Арендт Вильям；Бегз Дональд
    申请人:Мидрекс Корпорейшн (Фирма)；
    IPC主号:
    专利说明:

    (5 method of DIRECT IRON RESTORATION WHEN USING HIGH-GRAND GAS The direct reduction of iron oxide from agglomerated pellets or lump ore to metallic gall in a solid state in recent years has become a reality in many factories of direct reduction all over the world. in operation or under construction, more than 15 million tons in. - recalculated for the metallized product of direct reduction of iron, which is used as a mixture for electric arc steelmaking furnaces. The global need for this additional reclaimed iron has a tendency to increase significantly over many years to meet the growing need for such a charge, since additional steelmaking plants with electric arc furnaces are being built. direct reduction processors, uses natural gas as a reducing agent. Natural gas is processed to produce CO and H reducing agents. The most productive and most productive of direct reduction plants using technical natural gas are plants using the Midrex process, which involves the continuous catalysis of natural gas using CO as oxidizing agents and residual water vapor in a cooled, recirculated , spent reducing gas, exhaust from the reducing furnace. . The closest to the proposed technical essence and the achieved result is a method of direct reduction of iron, including a countercurrent of dispersed material loaded into the shaft furnace and hot sweet sulfur reducing gas consisting of a mixture of recirculated top gas and converted natural gases, followed by cooling of the reduced cooling gas recirculation 1. However, when converting natural gas or other gases containing hydrocarbons, it is necessary to maintain at a very low level the sulfur content in the gas mixture, which has been converted to eliminate catalyst poisoning. The maximum level of sulfur content allowed in the process is about 2-3 parts per million volume (million ppm) in the newly obtained mixture. To achieve such a low sulfur content is often difficult and expensive to desulfurize the gas, before it can be used as a fuel in the process. In many industrialized countries, coke oven gas is used as a fuel. However, it includes certain sulfur-containing components such as COS and. SdN Z-thiophene. In the proposed method, the Direct Reduction process is improved, since the gas for reduction is desulfurized in a reduction furnace in a new and more efficient way of reacting the sulfur contained in the process fuel / with hot direct repair iron before fuel is allowed in the converter. The sulfur contained in the process fuel is transferred to the iron during the recovery process. The allowable level of sulfur in the process fuel can reach 400 ppm without introducing an undesirable amount of sulfur into the iron reduction product. The on-site desulfurization of technological fuel makes it practically possible to use the S5 technology on the
    It is very difficult to desulfurize this fuel, outside of this process, for example, coke oven gas or surfactant gas is connected to several gas inlet openings located: - at a level exceeding the gas containing organic sulfur compounds. The reducing gas is introduced at two vertically separated levels, but at each level it has a different composition. In addition, both gases are introduced at the periphery of the shaft furnace and at different temperatures. The purpose of the invention is to increase the efficiency of the recovery process. The goal is achieved by using the method of direct reduction of iron using sour gas, which includes a countercurrent of material fed into the shaft furnace and hot sweet sulfur reducing gas consisting of a mixture of recycled flue gas. converted natural gases, subsequent cooling of the recovered product and recirculation of the cooling gas, desulfurization of methane containing gas is heated by heating to 600-775 ° C before mixing this gas with recycled, reducing and feeding the resulting mixture into the pre-reducing zone at a point above the supply of the main reducing gas stream. Sour gas is mixed with the entire reducing gas stream. The drawing shows the scheme of implementation of the method. The scheme includes a refractory lined refractory furnace 1 of mine type charge material meterial 2 of oxidized iron, i.e. pellets, pieces of natural ore, or a mixture of pellets and pieces of ore having a nominal particle size of mm are introduced into. feed hopper 3 and into the furnace through the loading pipe k to fill the furnace with charge 5- The direct reduction iron product is withdrawn from the lower part of the furnace through the discharge pipe 6 by means of a discharge conveyor 7- whose speed is regulated by the speed of passing the charge 5 through furnace 1, middle part of the pipe 1 is provided with an inlet pipe 8 for a hot reducing gas connected to several openings 9 for any gas in the refractory wall of the furnace. The inlet.- .. pipe 10 for the hot recovery of the location of the openings 9 The hot reducing gas, which consists of a mixture of hot recycled reducing ha and hot gaseous process fuel, introduced through the opening 11, is blown inwards and then moves upwards. descend you. The hot reducing gas introduced through the holes is also blown inwards and then moved upward against the descending charge. Hot reducing gas from holes 9 at. in its upward motion, first fills the cross section of the charge, and then concentrates approximately at the level of the hole 11 in the central area of the charge by injecting hot, pre-reducing gas through the holes 11. In the upper part of the seam two gas streams merge and fill all the cross section furnace heating and exiting the charge through the backfilling level 12 and then exiting the furnace through the top pipe 13 of the gas outlet. The top gas that leaves the furnace through the exhaust pipe 1 is a mixture of waste reducing gas and process gas fuel. In the lower part of the furnace 1, a cooling gas circuit is provided for cooling the direct reducing iron before unloading. This cooling circuit includes an inlet 1, connected to the cooling gas element 15, running inside the furnace 1, and a cooling gas 16 located inside the furnace above the distribution element, as well as the cooling gas outlet 17 and the external system gas circulation, having a scrubber-cooler 18 and a circulating fan 19. The overhead gas leaving the furnace 1 through the exhaust pipe 13 is cooled and cleaned of dust in the cooler-scrubber 20 and discharged through pipe 21. Most of the cooled The top gas passing through the pipe is compressed by compressor 22 and then injected into converter tube 23 made of heat-resistant alloy, one of which is shown in the drawing. Each converter tube is filled with pieces of refractory in the inlet of the tube, and the rest. 35 "Most are filled with nickel .... or a cobalt conversion catalyst 2k. Transducer tubes are enclosed. to a refractory furnace lined with refractory, having several burners 25 (one is shown) and a gas exhaust pipe 26 for removing burned gases, from the converter furnace in the burner. Most of the cooled top gases passing through the pipe 21 out of fuel from an external source 27, is sent to each burner through the pipe 28. The exhaust gases burned in the burner from the flue gas pipe 26 are used in a heat exchanger for preheating (not shown) intended for combustion air that enters each burner from the source 29. The heater 30 of gaseous process fuel, filled with heating pipes 31, made of a heat-resistant alloy (one is shown), is provided l heating up the gaseous process fuel coming from source 32. Heat is supplied to the heater from burners 33 (one is shown) fuel for combustion is supplied from source ZA., and air dll from source 35 is burned. Exhausted, burned in the burner, gas exits heater through the gas exhaust pipe Zb. Heated gaseous technology. The fuel is supplied to the reduction furnace 1 sequentially through pipes 37 and 38 and pipe 10 for the inlet of the reducing gas. The first, most of the gas exiting the tubes of the converter 23 is delivered to the inlet pipe 8 for the hot, reducing gas in the form of hot recycled second-, gas-reducing gas through the pipes 39 and kQ, the second, the smaller part of the hot gas,. converter 23, passes through the pipe and the valve, then mixes with the heated process gaseous fuel in the pipe 38, and this mixture becomes a hot pre-reducing gas that is fed to the furnace 1 through the inlet pipe 10. The process gas should s is heated to a sufficiently high temperaI f-V SE L1LCH .. I .t-III-bruwi (preferably above bZO s), tours MTOB process gas mixture II retracted g for the heated upper had a high temperature to effect direct reduction of iron oxide. The proposed method involves the complete mixing of a process gas containing sulfur, for example, coke gas, natural gas with a hot purified reducing gas to form a reducing gas mixture. This mixture is introduced into the recovery zone of the furnace through a single gas distribution and tuyere stock system. Such a process can be performed in the apparatus (see the drawing by closing the valve (3 on pipe 38). It is known that a large number of developed commercial processes for the removal of Nl5 (hydrogen sulfide) from such gases during a single desulfurization stage. However, the removal of COS (sulfur carbonyl) and organic sulfur compounds such as thiophene () requires the use of complex and multistage process to rogogo been ensured pipe LP
    batching for hydrogenation and treatment of sulfur compounds in HoS before these types of sulfur compounds can be removed.
    In laboratory experiments, it is possible that COS and organic sulfur compounds can be removed from gases by reacting with hot 1 pellets of reclaimed iron in the presence of hydrogen. Remanufactured iron at low temperatures is not effective for removing such sulfur compounds, but it is effective at temperatures of about 70 ° C and higher. The mechanism of this removal of Sulfur is not precisely known, but it can be assumed that hot, direct reduced iron becomes an effective catalyst for the transformation of these sulfur compounds in the presence of hydrogen into, which then chemically interacts with iron. In any case, sulfur passes from gas to direct-regenerated iron.
    Therefore, the gas mixture that is fed into the inlet pipe 10 must have a temperature in excess of about to remove sulfur.
    In the recovery furnace through the inlet pipe 8 at a temperature of about. The hot pre-reduction gas, which is a mixture of gas from the converter pipes and from the supply of coke gas having 750 ° C, from the heating pipes 31 flows into the recovery furnace through the inlet pipe 10 at a temperature of about 800 seconds. The design of the reduction furnace provides the residence time of the charge in the furnace for approximately A hr from the backfill level 12 to the holes. 11 and over a period of 6 hours from the backfill level 12 to the openings 9, with the result that the high degree of direct reduction of iron oxide to metallic iron is achieved in the pre-reduction zone above the openings 11 with the final direct reduction achieved in the recovery zone between the openings Y and 11.
    In the precautionary zone, CO and H, contained in the hot gas, and in the hot —.: Reducing, flowing upward, iron oxide is already being restored from the final reduction zone. 5 „8. . However, higher temperatures are preferred, since about 800 ° C is necessary for the direct reduction of iron oxide. Some pellets exhibit a tendency to slip at 800 ° C and should be reduced at lower temperatures. Practically, the lower limit of the gas temperature in the inlet pipe 8 is 750 C. The following is a special example using sulfur-containing coke oven gas as a process gaseous fuel, both as a fuel for burners and in a converter furnace and in a gaseous process fuel heater. The sulfur content accepted for the coke oven gas in this example is 200 ppm volume, which is the sulfur content typically achieved in a simple process and with one desulfurization stage. Gas with this sulfur content is technologically unsuitable for the conversion process, but it is very suitable as a burner fuel. The hot reducing gas from converter 23 enters contained in the charge, to a degree of metallization of approximately. Based on laboratory tests and technical experience, it has been established that the methane present in the pre-reduction gas from the coke oven gas does not disengage to any appreciable degree as it passes through the pre-reduction zone when it is equal to the hydrogen already present in the gas. Therefore, the exhaust gas or the top gas coming out of the furnace charge through the filling level and through the exhaust pipe 18, the gas from the furnace, unreacted reducing agents CO and H, oxidizing agents CO and the resulting reduction process, and methane B cooler scrubber 19 for the top most of the gas is condensed from the top gas, driven by the fact that the 5: 10 gas mixture becomes suitable for conversion in the tubes of the converter 23 to produce hot reducing gas. In the pipes of the SOL converter and the residual water vapor in the cooled and dust-free recirculated gas ;, they serve as the oxide of G1 for the conversion of methane .. In the table. Tables 1 and 3 show the results of a comprehensive analysis of the proposed method per ton, the product of direct reduction of iron, having a metallization degree of 92 and a carbon content of 1.5%. These are widely accepted technical standards for directly repaired iron produced on natural gas of direct reduction. In tab. Figure 1 shows the fuel consumption required for the process. Coke oven gas has the highest heat of combustion of ft6l8 kcal / m (19318 kJ / m). . blitz
    Total demand fuel efficiency 3.21
    In tab. 2 shows data on gas flows in the process at designated locations in the drawing, ..,
    Table 2.
    Flow rate
    Gas
    From transducer (, yo)
    At the lower exhaust pipes (1)
    Converted gas from the top exhaust pipes (k2)
    Hot gas for heating (38)
    13,
    i Continued table. 2
    Gas
    Flow rate
    45
    50
    55 In taol. Figure 3 shows the gas analysis data at designated locations located) ,; eni,%; Approximately .0,018 sulfur is added- 5
    with to metallized iron
    Converted gas (40) 32
    Technological top
    OR (38)
    6.8
    Upper prom
    pipes (39)
    Upper Gas (13)
    Refined gas
    In the proposed method, natural gas is used as the gaseous process fuel instead of coke oven gas, the required volumetric amount of which is about half of the coke oven gas due to almost twice the calorific value of the HFO gas. At the same time, in natural gas, a content of approximately iOO million volume is permissible without introducing an excessive amount of sulfur into the iron-containing product.
    权利要求:
    Claims (1)
    [1]
    1. A method of direct reduction of iron using a high-sulphurous giz, including a countercurrent of material loaded into the shaft furnace on top of it and a hot, desulfurized reducing gas consisting of a mixture of recirculated steel stock production.
    AZ Tables
    B96,2
    51,55.1
    5.33.0
    28.75,
    200
    53,23,8
    18,15,7 121
    3,323,4
    10,56,0
    2.74.5
    13,17,5
    recycled and converted natural gases, subsequent cooling of the recovered product and recirculation of the cooling gas, characterized in that, in order to increase the efficiency of the reduction process, the methane-containing gas is desulfurized by heating to 600-775 ° C before the gas is mixed with recycled reducing and by feeding the resulting mixture to the pre-reduction zone at a point above the main flow of the reducing gas.
    2, the method according to p. 1, about tl and h ayusch and and Sh, so that the sweet sulfur gas is mixed with the entire flow of the reducing gas.
    Sources of information taken into account in the examination
    1. US Patent No. 37A8G20, cl. From 21 to 13/60, published. 1979. product with the help of sulfur transfer from gaseous process fuel. This margin is 0.03% for the use of the iron direct reduction in the electrode
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    引用文献:
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    US4608240A|1983-11-04|1986-08-26|Hylsa, S.A.|Method for the desulfurization of hydrocarbon gas|
    US4536213A|1984-09-10|1985-08-20|Mildrex International, B.V.|Reforming of higher hydrocarbons for metal oxide reduction|
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    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    US06/086,980|US4270739A|1979-10-22|1979-10-22|Apparatus for direct reduction of iron using high sulfur gas|
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