CN113122671B - Method for controlling erosion of high-titanium molten iron converter slag on furnace lining - Google Patents

Method for controlling erosion of high-titanium molten iron converter slag on furnace lining Download PDF

Info

Publication number
CN113122671B
CN113122671B CN202110290357.8A CN202110290357A CN113122671B CN 113122671 B CN113122671 B CN 113122671B CN 202110290357 A CN202110290357 A CN 202110290357A CN 113122671 B CN113122671 B CN 113122671B
Authority
CN
China
Prior art keywords
slag
converter
furnace
gun
molten iron
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
CN202110290357.8A
Other languages
Chinese (zh)
Other versions
CN113122671A (en
Inventor
华福波
王劼
杨昌涛
陶昌德
伍从应
刘明波
杨龙飞
蓝桂年
文安义
郑新泉
陈浩
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shougang Shuicheng Iron and Steel Group Co Ltd
Original Assignee
Shougang Shuicheng Iron and Steel Group Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Shougang Shuicheng Iron and Steel Group Co Ltd filed Critical Shougang Shuicheng Iron and Steel Group Co Ltd
Priority to CN202110290357.8A priority Critical patent/CN113122671B/en
Publication of CN113122671A publication Critical patent/CN113122671A/en
Application granted granted Critical
Publication of CN113122671B publication Critical patent/CN113122671B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21CPROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
    • C21C5/00Manufacture of carbon-steel, e.g. plain mild steel, medium carbon steel or cast steel or stainless steel
    • C21C5/28Manufacture of steel in the converter
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21CPROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
    • C21C5/00Manufacture of carbon-steel, e.g. plain mild steel, medium carbon steel or cast steel or stainless steel
    • C21C5/28Manufacture of steel in the converter
    • C21C5/30Regulating or controlling the blowing
    • C21C5/32Blowing from above
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21CPROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
    • C21C5/00Manufacture of carbon-steel, e.g. plain mild steel, medium carbon steel or cast steel or stainless steel
    • C21C5/28Manufacture of steel in the converter
    • C21C5/36Processes yielding slags of special composition
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P10/00Technologies related to metal processing
    • Y02P10/20Recycling

Landscapes

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Carbon Steel Or Casting Steel Manufacturing (AREA)

Abstract

The invention belongs to the technical field of metallurgical steelmaking, and particularly relates to a method for controlling erosion of high-titanium molten iron converter slag on a furnace lining; by adopting the method of adding light-burned dolomite into a converter before adding the steel scrap and the molten iron, the slag remained in the last furnace and TiO formed by the blowing oxidation of the furnace are solidified2The erosion of the slag line on the furnace lining is reduced, a low-lance-position, large-flow and long-time lance pressing mode is adopted when a lance is pressed at the end point, the content of final slag (FeO) is reduced, and the erosion of the slag line on the furnace lining when the slag is poured into a converter and steel is tapped is controlled; meanwhile, a low-high-low slag splashing gun position mode is adopted, and the slag splashing furnace protection effect is ensured through three times of splashing and cooling. Make TiO not to contact with the surface of the substrate2The corrosion degree of the furnace lining is greatly reduced, the safety and the regularity of the furnace condition are ensured, the furnace protection frequency and the safety risk are directly reduced, the production rhythm of the converter is improved, the consumption of refractory materials is reduced, and the steel-making cost is saved.

Description

Method for controlling erosion of high-titanium molten iron converter slag on furnace lining
Technical Field
The invention belongs to the technical field of metallurgical steelmaking, and particularly relates to a method for controlling erosion of converter slag of a high-titanium molten iron converter on a furnace lining.
Background
The furnace age is an important economic and technical index for converter steelmaking, and directly influences the operation rate of converter steelmaking and the cost of refractory materials. In actual production, when the converter is smelted, the furnace lining refractory material is gradually thinned due to the impact of steel scrap and molten iron, the erosion and corrosion of high-temperature metal liquid, oxygen flow and furnace slag, so that the furnace shape, the smelting effect and the service life of the converter are influenced. In order to maintain a good furnace shape, ensure the normal flow field of molten metal and slag in the furnace and guarantee the metallurgical effect, the furnace shape maintenance work is required. However, the furnace protection consumes a large amount of refractory materials, occupies production time, influences production rhythm and increases production cost.
The titaniferous iron ore is an important strategic resource in western China, molten iron with high titanium content is obtained by blast furnace smelting, and titaniferous slag is generated by converter smelting due to TiO thereof2The service life of the lining of the converter is greatly influenced by the high content of the (acidic oxide) and the special physical and chemical properties. In the existing converter operation, the light-burned dolomite consumption is increased to carry out slag thickening and the converter protection frequency is increased to ensure that the furnace condition is safely controlled, and the operation mode has the defects of slow production rhythm, large light-burned dolomite consumption, high continuous casting tundish cost and the like.
From Ellingham' S oxygen bitmap (shown in FIG. 1), it is known that the oxidation sequence of the elements in molten iron is that Ti is first oxidized, then Si, V, Mn, Cr, P, S and the like are added, and Ti is oxidized to form TiO2And into the slag. TiO22In alkaline slag (R)>2.0) is acidic, and the Ti has small particle radius and large electrostatic potential and is easy to react with O released from alkaline oxides in slag2-The ions are combined to generate composite anions, and the anions are gradually combined into larger anion groups to increase the viscosity of the slag; and TiO22The dissolution of CaO and MgO in the slag is promoted, and the number of CaO and MgO particles precipitated in the slag due to supersaturation is reduced. Therefore, under the combined action of the two, the viscosity of the slag is changed along with the TiO when in non-reducing atmosphere2The increase of the content causes difficult thorough melting of the slag, which causes poor steel-slag separation effect at the end point of the converter, and the iron content of the slag is higher, which causes the consumption of iron and steel materials to rise and seriously restricts the slag splashing furnace protection effect. Furthermore, TiO2The influence on the semisphere temperature of the converter final slag is obvious, and the condition of measuring the melting point by sampling the slag is known, and every 1 percent of TiO in the slag is added2The slag melting point decreases by about 27 ℃. Converter final slag TiO2The content is 3-6%, and the hemisphere temperature is reduced by about 121.5 ℃. FIG. 2 shows FeO-CaO-V2O5The phase diagram of the ternary slag system shows the final slag V of the converter2O5When the content reaches more than 1.3 percent, the content has obvious influence on the melting temperature of the slag, finally the erosion resistance of a slag splashing layer is deteriorated when the slag splashing furnace protection is carried out, and the furnace condition of the converter is seriously deteriorated under the action of high temperature and peroxide slag. In order to maintain the furnace shape to ensure the metallurgical effect and the smelting safety of the converter, the furnace protection frequency must be increased, the furnace protection finished products are increased, and the production rhythm is influenced. The long furnace protection time greatly reduces the furnace temperature, the furnace entering heat needs to be increased for supplementing heat balance, the furnace type corrosion is easily aggravated again, and the increase of the furnace entering molten iron amount is inconsistent with the work of saving iron and increasing steel. Therefore, developing a new rapid furnace protection process which ensures the quality of the furnace protection and the smelting safety becomes one of the focus and the difficulty of improving the furnace protection effect of smelting the vanadium-titanium molten iron.
Patent document CN201810209687.8 discloses a method for reducing corrosion of converter lining, which comprises the steps of firstly adding dolomite into a converter, adding semisteel into the converter, then adding active lime, high-magnesium lime, an acidic composite slag former and waste slag of the converter into the converter while blowing, controlling the lance position of an oxygen lance and the oxygen blowing strength, and controlling the alkalinity of end-point slag to be 3-4 to obtain end-point molten steel and end-point slag. By adopting dolomite for slagging and adding the waste slag of the converter to replace part of metallurgical auxiliary materials, the TFe content in the end-point slag is reduced, the corrosion rate of the converter lining is obviously reduced, the service life of the converter is prolonged, and the smelting effect is not influenced. However, in practical application, it is found that if the basicity is calculated according to the calculation method, the actual basicity of the titanium-containing slag is relatively low, which is unfavorable for controlling the acid-base ratio of the slag, and the acid oxide in the slag in a free state is increased, which is unfavorable for controlling the corrosion of the slag to a molten pool and is also unfavorable for dephosphorization and desulfurization. And the titanium-containing slag is not only a problem of corrosion of the lining caused by TFe, but also TiO2It also has a large effect on the life of the converter lining.
Disclosure of Invention
The invention provides a method for controlling the erosion of the converter slag of the high-titanium molten iron converter to a furnace lining to solve the problems.
The method is realized by the following technical scheme:
a method for controlling the erosion of the slag of a high-titanium molten iron converter to a furnace lining comprises the following steps:
1. smelting in an early stage: 1000kg of light-burned dolomite is added into a converter with the slag amount of about 3000kg, the converter is stirred and fried with scrap steel, preheated and added with molten iron, the blowing gun position is 1.8m, and the oxygen supply flow is 22000m3H, adding light-burned dolomite after ignition is successful, wherein the adding system is as follows: when the titanium content in the molten iron is 0.050-0.150%, the addition amount of the light-burned dolomite is 0 kg; when the titanium content in the molten iron is 0.151-0.200%, the addition amount of the light-burned dolomite is 200 kg; when the titanium content in the molten iron is 0.201-0.250%, the addition amount of the light-burned dolomite is 300 kg; when the content of titanium in the molten iron is more than 250 percent, the addition amount of the light-burned dolomite is 500 kg. Adding 635-2290kg of lime, immediately reducing the lance position to 1.2m after reacting for 20s, then adding 70-300kg of sintering return ores into the furnace, judging blowing to 2.8-3.2min through the flame at the furnace mouth, removing slag, adding 270-980kg of lime, controlling the alkalinity to 1.8, and reducing the oxygen supply flow to 20000m3Reducing the gun position to 1.1m, and gradually increasing the gun position to 1.7m within 4-8min of blowing;
2. in the middle stage of smelting: lime is added in three batches within 4-6min of blowing, the total adding amount is 450-1290kg, and the alkalinity of the final slag is 2.5-3.2. The oxygen supply flow is recovered to 22000m within 8-11min of converting3And the gun position is periodically adjusted up and down between 1.3m and 1.7 m.
Further, the temperature of the molten iron is 1300-1410 ℃, the silicon content is 0.100-0.600%, and the titanium content is 0.150-0.400%.
Further, the alkalinity calculation method is optimized as R ═ CaO)/(% SiO)2+0.5(%TiO2))。
Further, the periodicity is controlled by 20s, specifically, the period is maintained for 20s at 1.7m, then decreased to 1.3m, then maintained for 20s, and then increased to 1.7m, and then maintained for 20s, and the total time is 3 min.
3. And (3) in the later stage of smelting: smelting to 10.5-11.5min, adding 200kg of light-burned dolomite, gradually reducing the lance position to 1.1m when reducing the lance position to 12min, adding 10kg of coke breeze into the furnace from a high-position stock bin, starting a constant point pressure lance to operate, wherein the lance pressure position is 1.1m, the oxygen supply flow is 23000m3And h, the gun pressing time is 55-65s, the gun is lifted to perform furnace reversing and slag pouring after the gun pressing is finished, and the slag pouring amount is about 40%.
4. Rocking the furnace and tapping: and (4) shaking the furnace to tap after deslagging is finished, and adding 5kg of carburant into the furnace after the converter stops stably to tap.
5. Slag splashing: after tapping is finished, the converter is shaken to a zero position, 10kg of coke is added into the converter from a high-position storage bin, then the converter is put into a gun for slag splashing operation, the slag splashing adopts a low-high-low gun position control mode, the lowest is 0.30-0.45m, the highest is 0.9-1.1m, the nitrogen flow is 29000m according to the low gun position3H, high gun position 27000m3And h, controlling the slag splashing time to be 2.0-2.5min, pouring all slag after the slag splashing operation is finished, measuring the thickness of the converter lining of the converter by using a converter shell thickness gauge, and comparing the measured value with the measured value of the last furnace.
FIG. 3 shows CaO-SiO2-TiO2The ternary slag system phase diagram shows that the slag is TiO2The content is 5%, when the binary alkalinity R is 1.2 and 0.64, the melting point of the slag is lowest; at the same time, the slag temperature and TiO2The content has a great influence on the viscosity, and the characteristic directly influences the steel-slag separation effect at the early stage of blowing. FIG. 4 shows the slag TiO at different temperatures2The influence of the content on the viscosity of the product can be seen from the analysis of the graph: the viscosity of the slag under different temperature conditions is dependent on TiO2The content is reduced with the increase of the content, and TiO is increased with the temperature of a molten pool2The influence of the content on the viscosity of the slag is reduced; TiO at 1400 deg.C2The influence of the content on the slag viscosity is most obvious, and the lower the content is, the greater the influence on the slag viscosity is.
Therefore, when smelting slag in the early stage of high-titanium molten iron production, [ Ti ] in molten iron]Rapidly oxidized to the slag and to the TiO2The slag is stable in slag, and the primary slag is low-alkalinity, multi-component and high-oxidizing slag. The more the mineral components of the primary slag are, the correspondingly lower the melting point is, the faster the slagging speed is, and the better the Ti removal effect is.
In conclusion, the beneficial effects of the invention are as follows: the invention adopts a method of adding light-burned dolomite into a converter before adding scrap steel and molten iron to solidify the slag remained in the last furnace and TiO formed by blowing and oxidizing in the last furnace2The erosion of the slag line on the furnace lining is reduced, a low-lance-position, large-flow and long-time lance pressing mode is adopted when a lance is pressed at the end point, the content of final slag (FeO) is reduced, and the erosion of the slag line on the furnace lining when the slag is poured into a converter and steel is tapped is controlled; meanwhile, a 'low-high-low' slag splashing gun position mode is adopted, and the slag splashing furnace protection effect is ensured through three times of splashing and cooling back and forth. Make TiO not to contact with the surface of the substrate2The corrosion degree of the furnace lining is greatly reduced, the safety and the regularity of the furnace condition are ensured, the furnace protection frequency and the safety risk are directly reduced, the production rhythm of the converter is improved, the consumption of refractory materials is reduced, and the steel-making cost is saved.
Wherein 1000kg of light-burned dolomite is preheated together with the scrap steel to promote melting. Solidifying the slag left in the last furnace and TiO formed by the blow-on oxidation of the furnace2The corrosion to the furnace lining is reduced; meanwhile, the method can control the over-slow temperature rise of a molten pool and poor slagging effect caused by adding a large amount of light-burned dolomite during blowing, and cannot fully utilize MgO in the light-burned dolomite to react a Ti-O reaction product TiO2Absorbing and solidifying to cause a large amount of the reaction to directly react with the furnace lining so as to erode the furnace lining. By lightly burning dolomite to fix titanium, TiO is reduced2The dephosphorization is influenced by the large consumption of lime, the reaction is prevented from generating a large amount of titanium-containing compounds with low melting points and poor stability, and a large amount of free TiO begins to be decomposed in the early stage of smelting2And erode the furnace lining. Aiming at the specific properties of the molten iron containing titanium and the actual production experience on site, the alkalinity calculation method is optimized to R ═ CaO/(% SiO)2+0.5(%TiO2) Alkalinity in earlier stage of smelting is controlled according to 1.8, and TiO is controlled2It is favorable for creating low alkalinity to the erosion of furnace lining. The alkalinity calculation formula was optimized to include the percent acidic oxide according to the TiO2 attribute. The basicity is closer to the molten iron smelting that contains titanium in this application, distinguishes with the non-ferrotitanium water basicity calculation mode, can effective control slag acid-base proportion, and then is the acid oxide of free state in the control slag, does benefit to the erosion that reduces the slag to the furnace lining, also does benefit to the dephosphorization desulfurization. In the early stage of smelting, proper iron-containing cold material (namely sintering return ores) is added according to the temperature of molten iron, and low-lance-position and high-flow operation is adopted, so that good dynamic conditions are improved, the temperature of a molten pool is quickly improved, and slag-steel separation is improvedThe effect is achieved; secondly, the higher content of FeO in the slag is kept, namely the slag is controlled according to an iron slag forming way, which is beneficial to the formation of initial slag and the TiO formation2Stably exists in the slag and controls the erosion of the furnace lining. 200kg of light-burned dolomite is added before the lance position is reduced in the later stage of smelting to control the decomposition of titanium-containing compounds in a high-temperature state and to control TiO in slag2And (5) solidifying to control the erosion of the furnace lining. When the gun is pressed at the end point, 10kg of coke is added into the converter, and a low-gun position, large-flow and long-time gun pressing mode is adopted to reduce the content of final slag (FeO) and form the low-iron titanium-containing converter final slag. The slag amount is controlled according to 60% of the total slag amount to be matched with a 100t converter model, 5kg (one bag) of carburant is thrown into the converter during the tapping process, the secondary oxidation of the slag during the tapping process can be controlled, the corrosion of the slag line of the converter lining during the tapping process is reduced, and the reduction of the melting point of the slag to further influence the slag splashing effect is avoided. The slag splashing method comprises the steps of adopting a low-high-low slag splashing gun position mode different from the conventional high-low slag splashing mode, splashing slag on a furnace lining while cooling the slag through a low gun position and a large flow rate, then increasing the gun position, reducing the flow rate, cooling a splashing layer to improve the adhesion effect, and finally adopting the low gun position to splash and cool the non-adhered slag again. The slag splashing furnace protection effect is ensured by three times of splashing and cooling. The furnace protection with medium and low alkalinity is realized by more accurate adding amount and mode control, and the consumption of corresponding slag charge is lower. The influence of the slag TFe on the erosion of the furnace lining is reduced, and the problem of the erosion of the furnace lining under the dual factors of the contents of the slag TiO2 and the TFe is reduced to a certain extent aiming at the special characteristics of the erosion of the furnace lining of the converter containing titanium molten iron.
Drawings
Fig. 1 is an Ellingham oxygen bitmap.
FIG. 2 shows FeO-CaO-V2O5Ternary slag system phase diagram.
FIG. 3 shows CaO-SiO2-TiO2Ternary slag system phase diagram.
FIG. 4 shows the slag TiO at different temperatures2The effect of the content on its viscosity.
FIG. 5 is SEM results of the final slag of example 1.
FIG. 6 is SEM results of the final slag of example 2.
FIG. 7 is the SEM results of the final slag of example 3.
FIG. 8 is SEM results of comparative example final slag.
Detailed Description
The following is a detailed description of the embodiments of the present invention, but the present invention is not limited to these embodiments, and any modifications or substitutions in the basic spirit of the embodiments are included in the scope of the present invention as claimed in the claims.
Example 1
A method for controlling the erosion of the slag of a high-titanium molten iron converter to a furnace lining comprises the following steps:
1. smelting in an early stage:
the slag amount is about 3000kg after the slag splashing of the previous furnace is finished, 1000kg of light-burned dolomite is added into the furnace from a high-position storage bin before the furnace enters the scrap steel, the light-burned dolomite is stir-fried with the scrap steel and is preheated, then molten iron is added, and the furnace entering conditions of the molten iron are shown in table 1. The position of the blow gun is 1.8m, and the oxygen supply flow is 22000m3H, adding 500kg of light-burned dolomite after successful ignition, adding 1470kg of lime after reaction for 20s, immediately reducing the lance position to 1.2m after reaction for 20s, then adding 300kg of sintered return ores into the furnace, judging blowing to 2.8min through the flame at the furnace mouth, slagging, adding 630kg of lime, controlling the alkalinity to be 1.8, and reducing the oxygen supply flow to 21000m3Reducing the gun position to 1.1m, and gradually increasing the gun position to 1.7m within 4-8min of blowing;
2. in the middle stage of smelting: lime is added into the blowing for 4min to 6min in three batches, the total addition is 1170kg, and the oxygen supply flow is recovered to 22000m within 8min to 11min of blowing3And the gun position is periodically adjusted up and down between 1.3m and 1.7 m.
Further, the periodicity is controlled by 20s, specifically, the period is maintained for 20s at 1.7m, then decreased to 1.3m, then maintained for 20s, and then increased to 1.7m, and then maintained for 20s, and the total time is 3 min.
3. And (3) in the later stage of smelting:
when smelting is carried out for 11min, 200kg of light-burned dolomite is added, the lance position is gradually reduced to 1.1m when the lance position is reduced to 12min, 10kg of coke is added into the furnace from a high-position stock bin, the coke is opened, the pressure is always on, the lance position is 1.1m, the oxygen supply flow is 23000m3And h, the gun pressing time is 61s, the gun is lifted to perform furnace reversing and slag pouring after the gun pressing is finished, and the slag pouring amount is about 40%.
4. And (4) rocking the furnace to discharge steel: and (4) shaking the furnace to tap after deslagging is finished, and adding 5kg of carburant into the furnace after the converter stops stably to tap.
5. Slag splashing: after tapping is finished, the converter is shaken to a zero position, 10kg of coke is added into the converter from a high-position storage bin, then the converter is put into a gun for slag splashing operation, the slag splashing adopts a low-high-low gun position control mode, the lowest gun position is 0.40m, the highest gun position is 1.0m, and the nitrogen flow is 29000m according to the low gun position3H, high gun position 27000m3And h, controlling the slag splashing time to be 2.2min, pouring all slag after the slag splashing is finished, measuring the thickness of the converter lining of the converter by using a converter shell thickness gauge, and comparing the measured value with the measured value of the last furnace time, wherein the thickness of the converter lining is increased by 18mm after the furnace time is smelted.
SEM results of converter final slag taken in a converter are shown in FIG. 5, and chemical compositions thereof are shown in Table 2, and it is understood from Table 2 that the final slag basicity is 2.74 and the (TFe) content is 14.23%, (TiO)2) The content is 3.13 percent, and the TiO slag in each stage of smelting can be known by combining the thickness of the furnace lining2The erosion degree of the furnace lining is greatly reduced.
Example 2
A method for controlling the erosion of the slag of a high-titanium molten iron converter to a furnace lining comprises the following steps:
1. smelting in an early stage:
the amount of slag remained after the slag splashing of the previous furnace is finished is about 3000kg, 1000kg of light-burned dolomite is added into the furnace from a high-level bunker before the furnace enters the waste steel, and the light-burned dolomite is stir-fried and preheated along with the waste steel and then added with molten iron, wherein the charging conditions of the molten iron are shown in table 1. The position of the blow gun is 1.8m, and the oxygen supply flow is 22000m3After ignition is successful, 300kg of light-burned dolomite is added, lime 1330kg is added after reaction for 20s, the lance position is immediately reduced to 1.2m after reaction for 20s, then 100kg of sintered return ores are added into the furnace, blowing is judged by the flame at the furnace mouth until 3.1min, slag is removed, at the moment, 570kg of lime is added,controlling alkalinity to 1.8, and reducing oxygen flow to 21000m3Reducing the gun position to 1.1m, and gradually increasing the gun position to 1.7m within 4-8min of blowing;
2. in the middle stage of smelting: lime is added into the blowing process for 4min to 6min for three times, the total adding amount is 970kg, and the oxygen supply flow is recovered to 22000m within 8min to 11min of the blowing process3And the gun position is periodically adjusted up and down between 1.3m and 1.7 m.
Further, the periodicity is controlled by 20s, specifically, the period is maintained for 20s at 1.7m, then decreased to 1.3m, then maintained for 20s, and then increased to 1.7m, and then maintained for 20s, and the total time is 3 min.
3. And (3) in the later stage of smelting:
when smelting is carried out for 11.05min, 200kg of light-burned dolomite is added, the lance position is gradually reduced to 1.1m when 12min, 9kg of coke breeze is added into the furnace from a high-level stock bin, the operation of a constant pressure lance is started, the lance position of the pressure lance is 1.1m, the oxygen supply flow is 23000m3And h, the gun pressing time is 58s, the gun is lifted to perform furnace reversing and slag pouring after the gun pressing is finished, and the slag pouring amount is about 40%.
4. Rocking the furnace and tapping: and (4) shaking the furnace to tap after deslagging is finished, and adding 5kg of carburant into the furnace after the converter stops stably to tap.
5. Slag splashing: after tapping is finished, the converter is shaken to a zero position, 10kg of coke is added into the converter from a high-position storage bin, then the converter is put into a gun for slag splashing operation, the slag splashing adopts a low-high-low gun position control mode, the lowest gun position is 0.35m, the highest gun position is 0.95m, and the nitrogen flow is 29000m according to the low gun position3H, high gun position 27000m3And h, controlling the slag splashing time to be 2.32min, pouring all slag after the slag splashing is finished, measuring the thickness of the converter lining of the converter by using a converter shell thickness gauge, and comparing the measured value with the measured value of the last furnace time, wherein the thickness of the converter lining is increased by 20mm after the furnace time is smelted.
SEM results of converter final slag taken in an inverted converter are shown in FIG. 6, and chemical components thereof are shown in Table 2. As is clear from Table 2, the final slag basicity is 2.63, (TFe) content is 15.12%, (TiO)2) The content is 3.06 percent, and the TiO slag in each stage of smelting can be known by combining the thickness of the furnace lining2The erosion degree of the furnace lining is greatly reduced.
Example 3
A method for controlling the erosion of the slag of a high-titanium molten iron converter to a furnace lining comprises the following steps:
1. smelting in an early stage:
the amount of slag remained after the slag splashing of the previous furnace is finished is about 3000kg, 1000kg of light-burned dolomite is added into the furnace from a high-level bunker before the furnace enters the waste steel, and the light-burned dolomite is stir-fried and preheated along with the waste steel and then added with molten iron, wherein the charging conditions of the molten iron are shown in table 1. The position of the blow gun is 1.8m, and the oxygen supply flow is 22000m3H, adding 300kg of light-burned dolomite after ignition is successful, adding 1250kg of lime after reaction for 20s, immediately reducing the lance position to 1.2m after reaction for 20s, then adding 70kg of sintered return ores into the furnace, judging blowing to 3.2min through the flame at the furnace mouth for slagging, adding 540kg of lime at the moment, controlling the alkalinity to be 1.8, and reducing the oxygen supply flow to 21000m3Reducing the gun position to 1.1m, and gradually increasing the gun position to 1.7m within 4-8min of blowing;
2. in the middle stage of smelting: lime is added into the blowing for 4min to 6min in three batches, the total adding amount is 1140kg, and the oxygen supply flow is recovered to 22000m within 8min to 11min of blowing3And the gun position is periodically adjusted up and down between 1.3m and 1.7 m.
Further, the periodicity is controlled by 20s, specifically, the period is maintained for 20s at 1.7m, then decreased to 1.3m, then maintained for 20s, and then increased to 1.7m, and then maintained for 20s, and the total time is 3 min.
3. And (3) in the later stage of smelting:
when smelting is carried out for 10.89min, 200kg of light-burned dolomite is added, the lance position is gradually reduced to 1.1m when 12min, 10kg of coke breeze is added into the furnace from a high-level stock bin, the operation of a constant pressure lance is started, the lance position of the pressure lance is 1.1m, the oxygen supply flow is 23000m3And h, the gun pressing time is 62s, the gun is lifted to perform furnace reversing and slag pouring after the gun pressing is finished, and the slag pouring amount is about 40%.
4. Rocking the furnace and tapping: and (4) shaking the furnace to tap after deslagging is finished, and adding 5kg of carburant into the furnace after the converter stops stably to tap.
5. Slag splashing: after tapping is finished, the converter is shaken to a zero position, 10kg of coke is added from a high-position storage bin, then the converter is put into a gun for slag splashing operation, and slag splashing adopts a low-high-low gun position control mode, wherein the lowest 0.38m and the highest 1m are adopted02m, nitrogen flow 29000m at low lance level3H, high gun position 27000m3And h, controlling the slag splashing time to be 2.27min, pouring all slag after the slag splashing is finished, measuring the thickness of the converter lining of the converter by using a converter shell thickness gauge, and comparing the measured value with the measured value of the last furnace time, wherein the thickness of the converter lining is increased by 21mm after the furnace time is smelted.
SEM results of converter final slag taken in a converter are shown in FIG. 7, and chemical compositions thereof are shown in Table 2, and it is understood from Table 2 that the final slag basicity is 2.86 and the (TFe) content is 14.87%, (TiO)2) The content is 3.48 percent, and the TiO slag in each stage of smelting can be known by combining the thickness of a furnace lining2The erosion degree of the furnace lining is greatly reduced.
Comparative example
1. Smelting in an early stage:
and (4) performing slag-leaving-free operation after the last slag splashing is finished, wherein the molten iron charging conditions are shown in Table 1. The position of the blow gun is 1.8m, and the oxygen supply flow is 21000m3And h, adding 1800kg of lime after ignition is successful, adding 1600kg of light-burned dolomite after reaction for 30s, reducing the gun position to 1.25m after reaction for 20s, judging blowing to 3.5min through furnace mouth flame, slagging, adding 600kg of lime and 200kg of light-burned dolomite at the moment, gradually increasing the gun position to 1.7m within 5-8 min of blowing, adding 400kg of lime into 5.1min of blowing, adding 400kg of lime into 6min of blowing, and regulating the gun position in a non-periodic manner within 1.3-1.7m for 8-12.5 min of blowing.
2. And (3) in the later stage of smelting:
when smelting is carried out for 12.57min, the lance position is reduced to 1.2m, the lance position is pressed to 1.2m, the lance position is started, the oxygen supply flow is 21000m3And h, the gun pressing time is 40s, the gun is lifted to perform furnace reversing and slag pouring after the gun pressing is finished, and the slag pouring amount is about 50%.
3. And (4) rocking the furnace to discharge steel: and after the slag pouring is finished, the furnace is shaken to tap steel, and no carburant is added.
4. Slag splashing: after tapping, slag splashing adopts a high-low gun position control mode, the lowest is 0.43m, the highest is 1.11m, and the nitrogen flow is 28000m3And h, the slag splashing time is 1.85min, after slag splashing is finished, all slag is poured out, the thickness of the converter lining of the converter is measured by using a converter shell thickness gauge, the thickness is compared with the measured value of the last furnace time, and the furnace after the furnace is smeltedThe thickness of the liner increases by 2 mm.
SEM results of final slag formation of converter taken in the converter are shown in FIG. 8, chemical compositions are shown in Table 2, and it is understood from Table 2 that the final slag basicity is 3.43, (TFe) content is 18.86%, (TiO)2) The content is 2.41 percent, and the TiO slag in each stage of smelting can be seen by combining the thickness of the furnace lining2The erosion to the furnace lining is serious.
TABLE 1 charging iron conditions
Figure BDA0002982235980000101
TABLE 2 slag composition after end of dephosphorization phase (wt%)
Figure BDA0002982235980000102

Claims (3)

1. A method for controlling erosion of high titanium molten iron converter slag to a furnace lining is characterized by comprising the following steps:
(1) smelting in an early stage: adding 1000kg of light-burned dolomite into a converter with a slag amount of 3000kg, stir-frying and preheating the converter along with scrap steel, adding molten iron, successfully adding the light-burned dolomite after ignition, reacting for 20s, adding lime twice, and adjusting the gun position and the flow rate;
after the ignition is successful, light-burned dolomite is added, and the addition system is as follows: when the titanium content in the molten iron is 0.050-0.150%, the addition amount of the light-burned dolomite is 0 kg; when the titanium content in the molten iron is 0.151-0.200%, the addition amount of the light-burned dolomite is 200 kg; when the titanium content in the molten iron is 0.201-0.250%, the addition amount of the light-burned dolomite is 300 kg; when the titanium content in the molten iron is more than 250 percent, the adding amount of the light-burned dolomite is 500 kg;
the lime is added twice, the first adding amount is 635-2290kg, and the second adding amount is 270-980 kg;
adding lime twice, reacting for 20s after adding lime for the first time, adding 70-300kg of sintered return ores into the furnace, blowing till slag is removed in 2.8-3.2min, and adding lime for the second time, wherein the target alkalinity is 1.8;
the gun position and flow rate adjusting method specifically comprises the following steps: the position of the blow gun is 1.8m, and the oxygen supply flow is 22000m3H; after the first lime addition, the reaction was carried out for 20s to reduce the lance height to 1.2 m; after the lime is added for the second time, the oxygen supply flow is reduced to 21000m3Lowering the gun position to 1.1m at the same time, and gradually increasing the gun position to 1.7m within 4-8min of blowing; recovering oxygen supply flow to 22000m in 8-11min3Adjusting the gun position periodically up and down between 1.3 and 1.7 m;
(2) in the middle stage of smelting: adding lime for the third time in three batches at 4-6min, wherein the total amount is 450-1290kg, and the alkalinity of the final slag is 2.5-3.2;
(3) and (3) in the later stage of smelting: adding 200kg of light-burned dolomite, reducing the gun position, adding 10kg of coke dices when the gun is pressed at the end point, and then reversing the furnace and deslagging;
the reduction of the lance position is to add light-burned dolomite when smelting is carried out for 10.5-11.5min, gradually reduce the lance position to 1.1m when smelting is carried out for 12min, and the oxygen supply flow is 23000m3/h;
The pressure gun at the end point is 1.1m in gun pressure position and 23000m in oxygen supply flow3The gun pressing time is 55-65 s;
(4) and (4) rocking the furnace to discharge steel: after the converter stops stably, adding 5kg of carburant into the converter, and tapping;
(5) slag splashing: the converter is shaken to a zero position, 10kg of coke is added, then a gun is put down for slag splashing operation, slag is poured out after slag splashing is finished, and the thickness of the converter lining of the converter is measured by using a converter shell thickness gauge;
the slag splashing adopts a low-high-low gun position control mode, and specifically comprises the following steps: minimum 0.30-0.45m and maximum 0.9-1.1m, nitrogen flow 29000m at low lance position3H, high gun position 27000m3H is controlled, and the slag splashing time is 2.0-2.5 min.
2. The method for controlling the erosion of the furnace lining by the molten iron converter slag with high titanium content as claimed in claim 1, wherein the temperature of the molten iron is 1300-1410 ℃, the silicon content is 0.100-0.600%, and the titanium content is 0.150-0.400%.
3. The method for controlling the erosion of the lining by the molten iron high-titanium converter slag according to claim 1, wherein the periodicity is controlled for 20s, specifically, the period is controlled to be 20s at 1.7m, then is reduced to 1.3m, then is maintained for 20s, then is increased to 1.7m, and then is maintained for 20s, and the total period is 3 min.
CN202110290357.8A 2021-03-18 2021-03-18 Method for controlling erosion of high-titanium molten iron converter slag on furnace lining Active CN113122671B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202110290357.8A CN113122671B (en) 2021-03-18 2021-03-18 Method for controlling erosion of high-titanium molten iron converter slag on furnace lining

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202110290357.8A CN113122671B (en) 2021-03-18 2021-03-18 Method for controlling erosion of high-titanium molten iron converter slag on furnace lining

Publications (2)

Publication Number Publication Date
CN113122671A CN113122671A (en) 2021-07-16
CN113122671B true CN113122671B (en) 2022-05-20

Family

ID=76773408

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202110290357.8A Active CN113122671B (en) 2021-03-18 2021-03-18 Method for controlling erosion of high-titanium molten iron converter slag on furnace lining

Country Status (1)

Country Link
CN (1) CN113122671B (en)

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102816887A (en) * 2012-08-22 2012-12-12 首钢水城钢铁(集团)有限责任公司 Method for directly smelting high-titanium molten iron by using converter
CN105177217A (en) * 2015-08-20 2015-12-23 山东西王特钢有限公司 Process for reducing steel slag quantity during converter smelting
CN107090535A (en) * 2017-05-24 2017-08-25 首钢总公司 A kind of converter smelting high phosphorus titaniferous molten iron protects the control method of carbon tapping
CN108330243A (en) * 2018-03-14 2018-07-27 攀钢集团攀枝花钢铁研究院有限公司 A method of it reducing converter lining and corrodes
CN109897933A (en) * 2019-04-04 2019-06-18 中天钢铁集团有限公司 A kind of efficient smelting process of the low-phosphorous clean steel of converter producing
CN110373511A (en) * 2019-07-17 2019-10-25 邯郸钢铁集团有限责任公司 A kind of converter smelting process of low lime consumption

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102816887A (en) * 2012-08-22 2012-12-12 首钢水城钢铁(集团)有限责任公司 Method for directly smelting high-titanium molten iron by using converter
CN105177217A (en) * 2015-08-20 2015-12-23 山东西王特钢有限公司 Process for reducing steel slag quantity during converter smelting
CN107090535A (en) * 2017-05-24 2017-08-25 首钢总公司 A kind of converter smelting high phosphorus titaniferous molten iron protects the control method of carbon tapping
CN108330243A (en) * 2018-03-14 2018-07-27 攀钢集团攀枝花钢铁研究院有限公司 A method of it reducing converter lining and corrodes
CN109897933A (en) * 2019-04-04 2019-06-18 中天钢铁集团有限公司 A kind of efficient smelting process of the low-phosphorous clean steel of converter producing
CN110373511A (en) * 2019-07-17 2019-10-25 邯郸钢铁集团有限责任公司 A kind of converter smelting process of low lime consumption

Also Published As

Publication number Publication date
CN113122671A (en) 2021-07-16

Similar Documents

Publication Publication Date Title
CN102828098A (en) Method for increasing molten steel finishing point manganese content by adding manganese ore outside furnace
CN110387448A (en) A kind of method that converter rapid low consumption produces low-phosphorous special steel
US3198624A (en) Process for the manufacture of stainless steel
US6693947B1 (en) Method to protect the anode bottoms in batch DC electric arc furnace steel production
CN113913583B (en) Slag modification and slag splashing furnace protection method
CN111286577A (en) Smelting method of ultra-low titanium steel
US3323907A (en) Production of chromium steels
CN111748670B (en) Method for improving chromium ore reduction by bottom blowing oxygen-lime powder
CN113122671B (en) Method for controlling erosion of high-titanium molten iron converter slag on furnace lining
CN1373229A (en) Method for smelting stainless steel with waste steel by frequency-conversion electric induction furnace
CN103205522B (en) Method for smelting plain carbon steel from semi-steel
CN103643094A (en) Smelting method of high-carbon ferromanganese
CN111961791A (en) Method for producing low-phosphorus steel by smelting high-phosphorus high-titanium molten iron in converter
US3499755A (en) Method for the production of pig iron and steel
CN103725821A (en) Method for prolonging life of vanadium-and-titanium-containing semi-steel making converter
CN103964437B (en) A kind of method controlling titanium carbide slag production process furnace bottom rising
US4115109A (en) Secondary lead smelting process
CN113462844B (en) Less-slag smelting method of titanium-containing molten iron converter
CN102140567B (en) Argon-oxygen refining method for low-carbon ferrochromium alloy
KR102628195B1 (en) Molten steel manufacturing method
CN114807497A (en) Method for smelting high-silicon molten iron by using bottom oxygen blowing and lime powder combined blowing converter
JPS61166910A (en) Production of chromium-containing alloy
Steenkamp et al. Introduction to the production of clean steel
CN113337662A (en) Method for improving dephosphorization effect of titanium-containing high-phosphorus molten iron converter in dephosphorization period
CN111893247A (en) Steelmaking method with high-efficiency refining function

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant