Classifications

• • C—CHEMISTRY; METALLURGY
  • C21—METALLURGY OF IRON
  • C21B—MANUFACTURE OF IRON OR STEEL
  • C21B3/00—General features in the manufacture of pig-iron
  • C21B3/04—Recovery of by-products, e.g. slag
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
  • C22B7/00—Working up raw materials other than ores, e.g. scrap, to produce non-ferrous metals and compounds thereof; Methods of a general interest or applied to the winning of more than two metals
  • C22B7/001—Dry processes
• • C—CHEMISTRY; METALLURGY
  • C21—METALLURGY OF IRON
  • C21B—MANUFACTURE OF IRON OR STEEL
  • C21B13/00—Making spongy iron or liquid steel, by direct processes
  • C21B13/10—Making spongy iron or liquid steel, by direct processes in hearth-type furnaces
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
  • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
  • Y02P10/00—Technologies related to metal processing
  • Y02P10/10—Reduction of greenhouse gas [GHG] emissions
  • Y02P10/122—Reduction of greenhouse gas [GHG] emissions by capturing or storing CO2
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
  • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
  • Y02P10/00—Technologies related to metal processing
  • Y02P10/10—Reduction of greenhouse gas [GHG] emissions
  • Y02P10/134—Reduction of greenhouse gas [GHG] emissions by avoiding CO2, e.g. using hydrogen
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
  • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
  • Y02P10/00—Technologies related to metal processing
  • Y02P10/20—Recycling
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
  • Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
  • Y02W10/00—Technologies for wastewater treatment
  • Y02W10/40—Valorisation of by-products of wastewater, sewage or sludge processing
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10S75/00—Specialized metallurgical processes, compositions for use therein, consolidated metal powder compositions, and loose metal particulate mixtures
  • Y10S75/962—Treating or using mill scale

Definitions

• the present invention relates to a process for the thermal treatment of residues containing oil and iron oxide, in the form of oil-containing sludges such as e.g. Sludges from steel mills.
• oil means mainly lubricants and greases that are used when rolling steel. They are therefore mainly hydrocarbons containing various additives as are common in lubricants.
• the object of the present invention is therefore to propose a method for the thermal treatment of such residues containing oil and iron oxide.
• This object is achieved according to the invention by a method for the thermal treatment of oil and iron oxide-containing residues in a deck oven which has a plurality of superposed floors, the oil and iron oxide-containing residues being mixed with a solid reducing agent and continuously introduced into the deck oven and onto the top floor applied and gradually transferred to the lower floors, drying the residues containing oil and iron oxide on the top floors, then evaporating and pyrolyzing the oil and reacting the reducing agents with the iron oxides to form directly reduced iron, whereby directly reduced iron is discharged together with residues of reducing agents in the area of the bottom floor of the deck oven.
• An important advantage of the invention is that valuable substances are produced from essential components of the oil and iron oxide-containing residues. After the process has been completed, the iron content can be returned to the steel mill's production process, the oil is pyrolyzed and the pyrolysis gases produced are burned. The oil thus helps to generate the necessary process heat. What may remain is ash, which essentially consists of inert substances such as SiO 2, I 2 O 3, MgO, ... and possibly an excess of reducing agents
• sludge-like, oil- and iron oxide-containing residues can be added, whereby caking of the particles is avoided by a targeted process control and by constant circulation. Regardless of the consistency of the input material, the process delivers a fine-grained end product.
• the iron obtained can then be processed into briquettes or placed directly in a melting furnace (electric furnace, etc.) and processed further.
• the resulting residues of the reducing agent can, if desired, be used in a separate gasification reactor with any unused reducing agents contained therein, the ash-forming constituents advantageously being separated out as liquid slag and the raw gas formed in the deck oven used as combustion or reducing gas. It is therefore also possible to use a cheaper reducing agent which has a relatively high ash content and / or to work with a relatively high excess of reducing agent, which prevents the agglomeration of the residues.
• part of the reducing agent required can also be applied to one or more floors, which are located below in the furnace.
• coarse-grained reducing agents (1 -3 mm) are introduced further up in the deck oven and fine-grained reducing agents ( ⁇ 1 mm) are added below.
• fine-grained reducing agents ⁇ 1 mm
• the reducing gases in the furnace can be adjusted to an optimal concentration, whereby a better degree of metallization can be achieved.
• the process room is divided into different zones, the solids move continuously from top to bottom and the gases are passed through the furnace from bottom to top.
• the process conditions in the different zones or even per floor can be measured and, if necessary, influenced in a targeted manner.
• the oil and iron oxide residues are continuously circulated by rakes attached to each floor of the furnace and gradually transported to the floor below.
• the constant circulation prevents the reducing agents and the oil and iron oxide-containing residues from caking together.
• the rate of circulation depends on many factors such as. B. the geometry of the rake, the thickness of the layers, etc.
• the oil and iron oxide-containing residues, the reducing agents and any reduced iron on the floors should be circulated at least once every one to three minutes, which largely prevents agglomeration.
• oxygen-containing gases that have a temperature of at least 250 ° C.
• a gaseous reducing agent can also be blown in on the lowest floors of the deck oven. This achieves a more complete reduction in oxides.
• one or more floors in the furnace are heated by means of a burner.
• gases are extracted from the deck oven on one or more floors. These hot gases can then either be passed through a CO 2 scrubber to reduce the amount of gas and increase the reduction potential of the gas, or passed through an additional reactor containing carbon so that it is contained in the hot gases Carbon dioxide reacts with the carbon to form carbon monoxide according to Boudoir's equilibrium, thereby increasing the reduction potential of the gas. The gases enriched with carbon monoxide are then returned to the deck oven.
• additives are added to one or more floors in the lower area of the furnace.
• gases are sucked out of the deck oven below a certain floor and then blown back into the oven above this floor.
• Carbon and heavy metal-containing iron oxide dusts or sludges can be introduced into the furnace on this level. As soon as they have reached a certain temperature (approx. 900 ° C) the heavy metal oxides begin to react with the reducing agents, forming heavy metals which volatilize and are discharged together with the exhaust gases from the deck oven.
• the heavy metals are advantageously extracted on the floors where they are formed and treated separately from the other exhaust gases.
• the exhaust gases are then e.g. oxidized in an afterburning chamber, the heavy metals being converted to heavy metal oxides which can then be separated from the exhaust gases in a filter device.
• Typical compositions of heavy metal dusts and sludges from electrical or converter steelworks are shown in the following table.
• the deck oven can be operated under a certain excess pressure.
• a rotary kiln which is sealed over water cups with a diameter of approximately 50 m, this is very easy to achieve in a deck oven that only has small seals on the drive shaft. In such a case, pressure locks must be provided for the input and export of material.
• Fig. 1 a section through a deck oven for the thermal treatment of residues containing oil and iron oxide.
• Fig. 1 shows a section through a deck oven 10, which has several - in this case twelve - superposed floors 12. These self-supporting levels 12, as well as the jacket 14, cover 16 and the bottom 18 of the furnace 10 are made of refractory material.
• a vent 20 is provided through which the gases can be evacuated from the furnace and an opening 22 through which a mixture of residues and reducing agents containing oil and iron oxide can be applied to the top floor.
• the rakes 26 are designed so that they roll the material from the outside inwards on one floor and then from the inside out on the floor below, so as to transport the material through the furnace 10 from top to bottom.
• the residues containing oil and iron oxide are mixed with solid reducing agents such as e.g. Lignite coke, petroleum coke, or coal are mixed and then the mixture of residues containing oil and iron oxide and reducing agent is applied to the top floor. Because of the viscous, sticky consistency of the mixture, it is introduced into the deck oven by means of pumps (not shown).
• solid reducing agents such as e.g. Lignite coke, petroleum coke, or coal are mixed and then the mixture of residues containing oil and iron oxide and reducing agent is applied to the top floor. Because of the viscous, sticky consistency of the mixture, it is introduced into the deck oven by means of pumps (not shown).
• the oil and iron oxide residues can possibly be pre-dried outside the oven before or after they are mixed with the solid reducing agents.
• the mixture of oil and iron oxide-containing residues and reducing agents After the mixture of oil and iron oxide-containing residues and reducing agents has been applied to the first floor of the furnace 10, it is circulated by the rakes 26 and transported to the edge of the floor, from where it falls through a plurality of openings 28 provided therefor onto the floor below. From there, the oil and oil mixed with reducing agents residues containing iron oxide are transported to the middle of the floor and then fall to the floor below. During transportation, the residues containing oil and iron oxide and the reducing agents are gradually heated.
• the shaft 24 and the rakes 26 are air-cooled and openings are provided on the rakes through which air can flow into the interior of the furnace and can be used there for afterburning.
• At least one inlet opening 30 is provided in the side walls of the furnace 10, usually in the upper third, through which additional reducing agents can be introduced into the furnace.
• These reducing agents can be in gaseous form or in liquid or solid form.
• These additional reducing agents are, for example, carbon monoxide, hydrogen, natural gas, petroleum and petroleum derivatives, or solid carbon carriers such as e.g. around brown coal coke, petroleum coke, blast furnace dust, coal, etc.
• the reducing agent in this case coal, is placed on a lower part of the furnace
• Nozzles 30 for blowing hot (250 ° C. to 500 ° C.) oxygen-containing gases are provided in the side wall, through which air or another oxygen-containing gas can be introduced into the furnace 10. Due to the high temperatures and the presence of oxygen, part of the carbon burns to carbon dioxide, which in turn reacts with the excess carbon and is converted to carbon monoxide. The carbon monoxide finally reduces the oxides.
• burners 32 are installed in the lower part of the furnace, which ensure a consistently high temperature in the lowest levels of the furnace. Gas or coal dust burners can be used here.
• These burners 32 can be fired with air for preheating and / or for additional heating with gas or coal dust.
• An additional reducing gas can be generated by the quantitative ratio between oxygen and fuel, or if the process gases are excess air, the process gases are re-burned.
• an excess of carbon monoxide can be generated in the burner.
• With external combustion chambers it can be avoided that the ashes of the burned coal get into the furnace and mix with the iron.
• the temperatures in the combustion chambers are chosen so that the slag can be drawn off in liquid form and can be disposed of in a glazed form.
• the iron produced is then discharged through the outlet 46 in the bottom 18 of the furnace 10 together with the ash.
• the iron discharged at the outlet 46 is cooled in a cooling device 48 with the ash and possibly still usable reducing agents.
• the reduced iron is then separated from the ashes of the reducing agents and any reducing agents which can still be used by a magnetic separator device 50.
• Reducers 52 that can be used are then burned in an external combustion chamber 34.
• the gases resulting from the combustion of the reducing agents can in turn be introduced into the furnace 10, while the residues of the reducing agents are discharged as ash or liquid slag through an outlet.
• the gas mixture from the furnace passes through the exhaust 20 into an afterburner 54, where the combustible gases of the gas mixture are burned.
• the gas mixture is then introduced into a cooling device 56 to which a cooling medium is applied and cooled.
• the cooled gas mixture is then cleaned using a cyclone filter 58 before it is discharged to the outside.
• this furnace 10 also allows various problem wastes, such as Recycle contaminated dusts containing iron oxide.
• Converter steelworks which contain hardly any carbon, or dust from the exhaust gas cleaning of blast furnaces, through a special opening 30 in the furnace 10 be introduced.
• the small volume of gas with a relatively high content of heavy metals can then be cleaned separately. Due to the small amounts of exhaust gas, low gas velocities occur on the corresponding floors, and so little dust is discharged with this exhaust gas. This results in a very high concentration of heavy metals in the exhaust gas.
• the combustible gases of the withdrawn gas mixture are burned in an afterburner 66.
• the remaining part of the gas mixture is cooled in a cooling device 68 and then cleaned with the aid of a cyclone filter 70 before it is released.
• the iron oxide contained in the dusts is reduced to iron with the waste containing oil and iron oxide.
• All rising gases, including the volatile constituents of the reducing agents, can be stored outside the deck oven in the drying system for the heavy metal and iron oxide-containing residues and, if necessary, for the reducing agents can be completely burned and the residual heat of the furnace exhaust gases can be optimally used.

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• Chemical & Material Sciences (AREA)
• Engineering & Computer Science (AREA)
• Organic Chemistry (AREA)
• Metallurgy (AREA)
• Materials Engineering (AREA)
• Manufacturing & Machinery (AREA)
• Mechanical Engineering (AREA)
• Geology (AREA)
• Life Sciences & Earth Sciences (AREA)
• General Life Sciences & Earth Sciences (AREA)
• Environmental & Geological Engineering (AREA)
• Manufacture And Refinement Of Metals (AREA)
• Manufacture Of Iron (AREA)
• Processing Of Solid Wastes (AREA)
• Treatment Of Sludge (AREA)
• Incineration Of Waste (AREA)
• Waste-Gas Treatment And Other Accessory Devices For Furnaces (AREA)
• Furnace Details (AREA)

Applications Claiming Priority (3)

Publications (1)

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• 1998
  • 1998-09-02 LU LU90282A patent/LU90282B1/de active
• 1999
  • 1999-01-14 TW TW88100505A patent/TW452598B/zh not_active IP Right Cessation
  • 1999-08-30 US US09/786,272 patent/US6391088B1/en not_active Expired - Fee Related
  • 1999-08-30 EP EP99947271A patent/EP1114193A1/de not_active Withdrawn
  • 1999-08-30 PL PL99346336A patent/PL346336A1/xx unknown
  • 1999-08-30 JP JP2000569026A patent/JP2004538122A/ja active Pending
  • 1999-08-30 AU AU60795/99A patent/AU747819B2/en not_active Ceased
  • 1999-08-30 TR TR200101428T patent/TR200101428T2/xx unknown
  • 1999-08-30 CN CN99809734A patent/CN1312863A/zh active Pending
  • 1999-08-30 CA CA002339014A patent/CA2339014A1/en not_active Abandoned
  • 1999-08-30 WO PCT/EP1999/006382 patent/WO2000014286A1/de not_active Application Discontinuation
  • 1999-08-30 CZ CZ2001755A patent/CZ2001755A3/cs unknown
  • 1999-08-30 KR KR1020017002502A patent/KR20010073025A/ko not_active Application Discontinuation
  • 1999-08-30 SK SK279-2001A patent/SK2792001A3/sk unknown
  • 1999-08-30 BR BR9913608-2A patent/BR9913608A/pt not_active Application Discontinuation
• 2001
  • 2001-02-02 ZA ZA200100948A patent/ZA200100948B/en unknown

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