CN1298033A - AC plasma melting reduction process and equipment for direct smelting of ferroalloy with very low carbon content - Google Patents
AC plasma melting reduction process and equipment for direct smelting of ferroalloy with very low carbon content Download PDFInfo
- Publication number
- CN1298033A CN1298033A CN99120078A CN99120078A CN1298033A CN 1298033 A CN1298033 A CN 1298033A CN 99120078 A CN99120078 A CN 99120078A CN 99120078 A CN99120078 A CN 99120078A CN 1298033 A CN1298033 A CN 1298033A
- Authority
- CN
- China
- Prior art keywords
- smelting
- parts
- plasma
- furnace
- micro
- 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.)
- Granted
Links
- 238000003723 Smelting Methods 0.000 title claims abstract description 58
- 229910001021 Ferroalloy Inorganic materials 0.000 title claims abstract description 30
- 229910052799 carbon Inorganic materials 0.000 title claims abstract description 30
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 title claims abstract description 17
- 238000002844 melting Methods 0.000 title description 4
- 230000008018 melting Effects 0.000 title description 4
- 238000011946 reduction process Methods 0.000 title description 3
- 239000000843 powder Substances 0.000 claims abstract description 31
- 239000012141 concentrate Substances 0.000 claims abstract description 25
- 238000000034 method Methods 0.000 claims abstract description 22
- 239000007789 gas Substances 0.000 claims abstract description 20
- 229910000831 Steel Inorganic materials 0.000 claims abstract description 19
- 239000010959 steel Substances 0.000 claims abstract description 19
- 239000011651 chromium Substances 0.000 claims abstract description 18
- 229910052750 molybdenum Inorganic materials 0.000 claims abstract description 17
- 229910052721 tungsten Inorganic materials 0.000 claims abstract description 16
- 239000010439 graphite Substances 0.000 claims abstract description 15
- 229910002804 graphite Inorganic materials 0.000 claims abstract description 15
- 229910000519 Ferrosilicon Inorganic materials 0.000 claims abstract description 14
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims abstract description 14
- 229910052804 chromium Inorganic materials 0.000 claims abstract description 14
- 239000011733 molybdenum Substances 0.000 claims abstract description 14
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims abstract description 13
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims abstract description 13
- 239000010937 tungsten Substances 0.000 claims abstract description 13
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 12
- 235000008733 Citrus aurantifolia Nutrition 0.000 claims abstract description 9
- 235000011941 Tilia x europaea Nutrition 0.000 claims abstract description 9
- 239000004571 lime Substances 0.000 claims abstract description 9
- 239000012159 carrier gas Substances 0.000 claims abstract description 8
- 239000010436 fluorite Substances 0.000 claims abstract description 7
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 claims abstract description 6
- 239000000571 coke Substances 0.000 claims abstract description 6
- 229910052742 iron Inorganic materials 0.000 claims abstract description 6
- 229910052710 silicon Inorganic materials 0.000 claims description 14
- 239000010703 silicon Substances 0.000 claims description 11
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 10
- 239000004615 ingredient Substances 0.000 claims description 9
- 239000000395 magnesium oxide Substances 0.000 claims description 8
- 238000005507 spraying Methods 0.000 claims description 7
- 229910004261 CaF 2 Inorganic materials 0.000 claims description 6
- 229910000604 Ferrochrome Inorganic materials 0.000 claims description 6
- 229910001309 Ferromolybdenum Inorganic materials 0.000 claims description 6
- 229910001145 Ferrotungsten Inorganic materials 0.000 claims description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 6
- 239000002994 raw material Substances 0.000 claims description 5
- 239000002893 slag Substances 0.000 claims description 5
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims description 4
- 239000002245 particle Substances 0.000 claims description 4
- 229910004298 SiO 2 Inorganic materials 0.000 claims description 3
- 239000000463 material Substances 0.000 claims description 3
- 239000011819 refractory material Substances 0.000 claims description 3
- 239000000377 silicon dioxide Substances 0.000 claims description 3
- 239000007921 spray Substances 0.000 claims description 3
- 229910045601 alloy Inorganic materials 0.000 abstract description 2
- 239000000956 alloy Substances 0.000 abstract description 2
- 229910052751 metal Inorganic materials 0.000 abstract description 2
- 239000002184 metal Substances 0.000 abstract description 2
- 150000002739 metals Chemical class 0.000 abstract description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 8
- 239000000203 mixture Substances 0.000 description 7
- 229940098458 powder spray Drugs 0.000 description 5
- 239000003638 chemical reducing agent Substances 0.000 description 4
- 229910000640 Fe alloy Inorganic materials 0.000 description 3
- 241001062472 Stokellia anisodon Species 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000005265 energy consumption Methods 0.000 description 2
- 239000011812 mixed powder Substances 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 238000007670 refining Methods 0.000 description 2
- 229910000851 Alloy steel Inorganic materials 0.000 description 1
- 229910000599 Cr alloy Inorganic materials 0.000 description 1
- AHIVCQLQCIBVOS-UHFFFAOYSA-N [Fe].[W] Chemical compound [Fe].[W] AHIVCQLQCIBVOS-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000005275 alloying Methods 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 239000000788 chromium alloy Substances 0.000 description 1
- DYRBFMPPJATHRF-UHFFFAOYSA-N chromium silicon Chemical compound [Si].[Cr] DYRBFMPPJATHRF-UHFFFAOYSA-N 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- 238000010891 electric arc Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000005243 fluidization Methods 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000036316 preload Effects 0.000 description 1
Images
Landscapes
- Furnace Details (AREA)
- Manufacture And Refinement Of Metals (AREA)
Abstract
一种采用交流等离子熔融还原铬、钨、钼精矿直接冶炼微碳铁合金的方法和装置。冶炼装置为三相交流小孔石墨电极等离子炉,注入Ar气或焦炉煤气以作为载气体,其中一根电极兼作加料极,将铬精矿粉、或钼精矿粉、或钨精矿粉、硅铁粉、石灰和萤石等经电极中心孔喷入熔池。被还原的Cr,W和Mo等金属溶入被熔化的定量废钢屑或铁屑中,达到铁合金所需的合金目标值。整个熔融还原及铁合金化过程速度快、收得率高、成本低。A method and device for directly smelting micro-carbon ferroalloys by adopting AC plasma smelting reduction of chromium, tungsten and molybdenum concentrates. The smelting device is a three-phase AC small-hole graphite electrode plasma furnace, injecting Ar gas or coke oven gas as a carrier gas, and one of the electrodes is also used as a feeding electrode, and the chromium concentrate powder, or molybdenum concentrate powder, or tungsten concentrate powder , ferrosilicon powder, lime and fluorite are sprayed into the molten pool through the center hole of the electrode. The reduced metals such as Cr, W and Mo are dissolved into the quantitative scrap steel scrap or iron filings to reach the alloy target value required by the ferroalloy. The whole process of smelting reduction and ferroalloying has high speed, high yield and low cost.
Description
本发明属于等离子熔融还原技术,尤其涉及在交流等离子炉中进行熔融还原直接冶炼微碳铁合金的方法和装置。The invention belongs to the plasma smelting reduction technology, in particular to a method and a device for directly smelting micro-carbon ferroalloy by smelting reduction in an AC plasma furnace.
目前,国内外冶炼微碳难熔铁合金的方法,有用电炉法(冶炼钨铁),电炉或真空电阻炉法(冶炼微碳铬铁)和炉外金属热还原法(冶炼钼铁)等。为了获得微碳铁合金,采用非碳质原料作还原剂,如用硅铬合金冶炼微碳铬铁,用硅、铝作还原剂冶炼钼铁和钨铁。这类铁合金的还原温度和熔点都比较高。如钨铁的熔点在2800K以上,用电炉冶炼时呈半熔融状态,不能自流出炉外,冶炼时间很长,能耗过大。如上所述,在冶炼这类铁合金时,由于需要特殊的冶炼工艺,或需要用昂贵的非碳质原料作还原剂,或需要过高的能耗等等,从而导致这类铁合金的成本过高,最终也导致用这类铁合金作为合金添加剂的合金钢的成本过高。At present, the methods for smelting micro-carbon refractory ferroalloys at home and abroad include electric furnace method (smelting ferro-tungsten), electric furnace or vacuum resistance furnace method (smelting micro-carbon ferrochrome) and metallothermal reduction method outside the furnace (smelting ferromolybdenum). In order to obtain micro-carbon ferroalloys, non-carbon raw materials are used as reducing agents, such as using silicon-chromium alloys to smelt micro-carbon ferrochrome, and using silicon and aluminum as reducing agents to smelt ferromolybdenum and ferrotungsten. The reduction temperature and melting point of this type of iron alloy are relatively high. For example, the melting point of ferro-tungsten is above 2800K. It is in a semi-molten state when smelted in an electric furnace, and cannot flow out of the furnace by itself. The smelting time is very long and the energy consumption is too large. As mentioned above, when smelting such ferroalloys, the cost of such ferroalloys is too high due to the need for special smelting processes, or the need to use expensive non-carbonaceous raw materials as reducing agents, or the need for excessive energy consumption, etc. , Eventually also lead to the high cost of alloy steel using such iron alloys as alloying additives.
本发明的目的是提供一种快速、高效、简便和经济的在等离子电炉中进行铬、钨、钼精矿的熔融还原直接冶炼微碳铁合金的方法和装置。The object of the present invention is to provide a fast, efficient, simple and economical method and device for directly smelting micro-carbon ferroalloys through smelting reduction of chromium, tungsten and molybdenum concentrates in a plasma electric furnace.
为实现上述目的,本发明在工艺上所采用的技术方案是:在三相交流等离子炉内预先一次性装填完所需废钢屑或废铁屑,并加入铬精矿、或钨精矿、或钼精矿、硅铁、石灰和氧化镁,约占总炉容的2/3左右。In order to achieve the above-mentioned purpose, the technical solution adopted in the process of the present invention is: pre-load the required steel scrap or scrap iron scrap in the three-phase AC plasma furnace at one time, and add chrome concentrate, or tungsten concentrate, or Molybdenum concentrate, ferrosilicon, lime and magnesium oxide account for about 2/3 of the total furnace capacity.
在冶炼Cr55微碳铬铁时,炉料所用成分的含量百分及所用份额为:Cr2O3为52.10%的铬精矿100份;硅为75%的硅铁粉25~27份;废钢屑8~10份;CaO≥75%的石灰8~10份;MgO≥90%的氧化镁4~6份。When smelting Cr55 micro-carbon ferrochrome, the content percentage and proportion of the ingredients used in the furnace charge are: 100 parts of chrome concentrate with 52.10% Cr 2 O 3 ; 25-27 parts of ferrosilicon powder with 75% silicon; scrap steel shavings 8-10 parts; 8-10 parts of lime with CaO≥75%; 4-6 parts of magnesium oxide with MgO≥90%.
在冶炼W75钨铁时,炉料所用成分的含量百分及所用份额为:WO3为67.87%的钨精矿100份;硅为75%的硅铁粉21~23份;SiO2≥95%的硅石6~8份;CaF2≥85%的萤石2~3份;废钢屑4~5份。When smelting W75 ferro-tungsten, the content percentage and share of the ingredients used in the charge are: 100 parts of tungsten concentrate with WO 3 being 67.87%; 21-23 parts of ferrosilicon powder with 75% silicon; SiO 2 ≥ 95% 6-8 parts of silica; 2-3 parts of fluorite with CaF 2 ≥85%; 4-5 parts of steel scrap.
在冶炼Mo60钼铁时,炉料所用成份的含量百分及所用份额为:MoO3为69.82%的钼精矿100份;硅为75%的硅铁粉30~32份;CaO≥75%的石灰4~6份;CaF2≥85%的萤石1~2份;废钢屑15~17份。When smelting Mo60 molybdenum ferromolybdenum, the content percentage and proportion of the ingredients used in the charge are: 100 parts of molybdenum concentrate with MoO 3 being 69.82%; 30-32 parts of ferrosilicon powder with 75% silicon; lime with CaO≥75% 4-6 parts; 1-2 parts of fluorite with CaF 2 ≥85%; 15-17 parts of steel scrap.
等离子发生器所用载气体为Ar气,或焦炉煤气。焦炉煤气可以产生还原性等离子体,有利熔融还原过程。The carrier gas used in the plasma generator is Ar gas or coke oven gas. Coke oven gas can generate reducing plasma, which is beneficial to the smelting reduction process.
冶炼时,待炉料已大部熔化后,往等离子炉内添加经干燥和混匀过的粉状原料,控制粒度<20目。其方式是用流化喷粉装置通过一根小孔石墨电极均匀喷入等离子炉弧区。已还原的金属Cr、W和Mo溶入已熔化的废钢屑或废铁屑液中,达到规定牌号的铁合金目标值。During smelting, after most of the charge has been melted, add dried and mixed powdered raw materials into the plasma furnace to control the particle size to <20 mesh. The method is to use a fluidized powder spraying device to spray evenly into the plasma furnace arc area through a small hole graphite electrode. The reduced metals Cr, W and Mo are dissolved into the melted steel scrap or scrap iron liquid to reach the target value of the ferroalloy of the specified brand.
为实现发明目的,本发明在装置上采用的技术方案是:用于熔融还原铬、钨、钼精矿直接冶炼微碳铁合金的等离子炉,由三相交流等离子发生器和炉体两部分组成。该发生器由三根小孔石墨电极构成,三根电极互相平行地竖直安装,三根电极的园心呈等边三角形均匀布置。每根电极均可以作上下移动和平行移动,每种移动均能自锁。炉体由炉盖和园台形炉壳组成,内衬为高温耐火材料,炉盖和炉体用钢板焊接而成,通水进行冷却;炉盖上开有孔,以供电极插入和升降,炉底开有铁合金流出口和排渣口。In order to realize the purpose of the invention, the technical scheme adopted in the device of the present invention is: the plasma furnace used for smelting and reducing chromium, tungsten, and molybdenum concentrates to directly smelt micro-carbon ferroalloys consists of a three-phase AC plasma generator and a furnace body. The generator is composed of three graphite electrodes with small holes, the three electrodes are installed vertically parallel to each other, and the centers of the three electrodes are evenly arranged in an equilateral triangle. Each electrode can move up and down and parallel, and each movement can be self-locking. The furnace body is composed of a furnace cover and a garden-shaped furnace shell. The lining is made of high-temperature refractory materials. The furnace cover and the furnace body are welded with steel plates and cooled by water; the furnace cover has holes for the insertion and lifting of electrodes. There are ferroalloy outlets and slag outlets at the bottom.
三根石墨电极沿轴心钻一φ4~φ8mm小孔,以注入稳定流动的载气体。将三根石墨电极中的一根,作为喷粉加料极,孔的大小以满足粉料能顺利流动,并以一定的气粉比将粉料均匀喷入,使粉料在石墨电极端口流出时大部分被等离子高温熔融和还原为宜。Three graphite electrodes drill a small hole of φ4~φ8mm along the axis to inject a stable flow of carrier gas. One of the three graphite electrodes is used as the powder-spraying feeding electrode. The size of the hole is such that the powder can flow smoothly, and the powder is evenly sprayed in with a certain gas-powder ratio, so that the powder will be larger when it flows out of the graphite electrode port. It is advisable to partly be melted and reduced by plasma at high temperature.
由于采用上述技术方案,本发明具有如下一系列特点:Owing to adopting above-mentioned technical scheme, the present invention has following series of characteristics:
采用熔融还原不会产生已还原合金元素的重氧化,可以使铁合金中氧含量降至很低水平;The use of smelting reduction will not produce heavy oxidation of the reduced alloy elements, and can reduce the oxygen content in the iron alloy to a very low level;
采用硅铁粉作还原剂,钢中C含量可以一次降到微C铁合金中C含量的要求;采用流化喷粉装置将所有原料通过电极中心孔均匀喷入高温等离子体弧区,不仅熔融还原速度极快,而且减化了加料过程;Using ferrosilicon powder as the reducing agent, the C content in the steel can be reduced to the requirement of C content in the micro-C ferroalloy at one time; all raw materials are evenly sprayed into the high-temperature plasma arc area through the center hole of the electrode by a fluidized powder spraying device, not only melting and reducing The speed is extremely fast, and the feeding process is simplified;
采用三相交流低电压大电流变压器提供等离子体发生器所需电源,相同容量的普通电弧炉用变压器可以满足这一要求。因此,适应性广。Three-phase AC low-voltage and high-current transformers are used to provide the power required for the plasma generator, and the transformers for ordinary electric arc furnaces with the same capacity can meet this requirement. Therefore, it has wide adaptability.
采用本发明的小孔石墨电极,等离子弧引弧容易,而且弧体稳定,不受炉料影响。可以通过升降石墨电极调节等离子弧的弧长;亦可通过调节变压器的次极电压和载气流量来调节等离子体的功率和弧长,以满足冶炼工艺过程的要求。By adopting the small-hole graphite electrode of the present invention, the plasma arc is easy to start, and the arc body is stable without being affected by the charge. The arc length of the plasma arc can be adjusted by lifting the graphite electrode; the power and arc length of the plasma can also be adjusted by adjusting the secondary voltage of the transformer and the flow rate of the carrier gas to meet the requirements of the smelting process.
也可采用焦炉煤气替代Ar气作为载气体以产生还原性等离子体,有利于熔融还原过程的工艺要求,而且比Ar气更经济、适用。Coke oven gas can also be used instead of Ar gas as a carrier gas to generate reducing plasma, which is beneficial to the technological requirements of the smelting reduction process, and is more economical and applicable than Ar gas.
采用粉料入炉,对炉料不需造球制块,也不用加粘结剂,炉料适应性广,对需要的炉料品位、粒度和形状都没有特殊要求。The powder is used to enter the furnace, and there is no need to pelletize the furnace charge, and there is no need to add a binder. The charge has wide adaptability, and there are no special requirements for the grade, particle size and shape of the charge.
因此本发明可达到下列技术经济指标:Therefore the present invention can reach following technical and economic index:
1、冶炼时间<30分钟;1. Smelting time <30 minutes;
2、Cr回收率可达90~95%、W和Mo回收率可达96~98%;2. The recovery rate of Cr can reach 90-95%, and the recovery rate of W and Mo can reach 96-98%;
3、铁合金成本可降低1/3。3. The cost of ferroalloy can be reduced by 1/3.
其指标详见附表。Its indicators are detailed in the attached table.
现结合附图和实施例对本发明作进一步描述:Now in conjunction with accompanying drawing and embodiment the present invention will be further described:
图1是本发明的三相交流等离子熔融还原铬、钨、钼精矿直接冶炼微C铁合金工艺流程示意图。Fig. 1 is a schematic diagram of the process flow of direct smelting of micro-C ferroalloy by three-phase AC plasma smelting reduction of chromium, tungsten and molybdenum concentrates of the present invention.
图2是本发明的三相交流等离子熔融还原铬、钨、钼精矿直接冶炼微碳铁合金的装置结构示意图。Fig. 2 is a schematic diagram of the structure of the device for direct smelting of micro-carbon ferroalloys by three-phase alternating current plasma smelting reduction of chromium, tungsten and molybdenum concentrates of the present invention.
本发明的工艺流程如图1所示:Process flow of the present invention is as shown in Figure 1:
第一步,先将粒度<20目的铬、钨、钼精矿粉、硅铁粉和熔剂,在120℃以内进行干燥,经配料后进行混匀,干燥的目的是保证粉料在喷粉罐内顺利流化和输送,也保证配料准确。The first step is to dry chromium, tungsten, molybdenum concentrate powder, ferrosilicon powder and flux with a particle size of <20 mesh at 120°C, and then mix them evenly after batching. Smooth fluidization and transportation inside, and also ensure accurate ingredients.
第二步,将废钢屑或废铁屑按配料需要一次装入炉内,再加入部分混合料,填充到整个炉容的2/3左右。其余粉料装入喷粉罐,并用Ar气充压流化。In the second step, the steel scrap or scrap iron scrap is loaded into the furnace at one time according to the batching requirements, and then part of the mixture is added to fill up to about 2/3 of the entire furnace volume. The rest of the powder is put into the powder spray tank and pressurized and fluidized with Ar gas.
第三步,等离子熔融还原。先是往小孔石墨电极中注入Ar气,启动变压器电源(变压器为三相交流低电压大电流变压器),引等离子弧。约5分钟后,当等离子炉内的炉料已基本熔融并充满等离子体时,开启喷粉罐下料球阀喷入其余的混合粉料,控制气粉比合适,使粉料一经离开电极端口即能被高温等离子体弧熔融和还原。然后调节电极高度,采用等离子埋弧精炼,并适当降低所用等离子体功率。The third step is plasma smelting reduction. First, inject Ar gas into the graphite electrode with small holes, start the transformer power supply (the transformer is a three-phase AC low-voltage high-current transformer), and start the plasma arc. After about 5 minutes, when the charge in the plasma furnace is basically melted and filled with plasma, open the ball valve of the powder spray tank to spray the rest of the mixed powder, and control the gas-powder ratio properly so that the powder can be discharged as soon as it leaves the electrode port. Melted and reduced by high temperature plasma arc. Then adjust the electrode height, adopt plasma submerged arc refining, and reduce the plasma power used appropriately.
第四步,提升电极、停电、停气、出钢、出渣。The fourth step is to lift the electrode, cut off the power, stop the gas, tap the steel, and tap the slag.
实施例1Example 1
在冶炼Cr55微碳铬铁时,炉料所用成分的含量百分及所用份额为:Cr2O3为52.10%的铬精矿100份;硅为75%的硅铁粉25份;废钢屑8份,CaO≥75%的石灰8份;MgO≥90%的氧化镁4份。得到的铬铁成分为:Cr为55~57%,C为0.1~0.25%,Si≤1.0~1.5%,S<0.02%,P<0.02%;Cr的收得率为90~95%。When smelting Cr55 micro-carbon ferrochrome, the content percentage and share of the ingredients used in the charge are: 100 parts of chrome concentrate with 52.10% Cr 2 O 3 ; 25 parts of ferrosilicon powder with 75% silicon; 8 parts of steel scrap , 8 parts of lime with CaO≥75%; 4 parts of magnesium oxide with MgO≥90%. The composition of the obtained ferrochrome is as follows: 55-57% of Cr, 0.1-0.25% of C, Si≤1.0-1.5%, S<0.02%, P<0.02%; the yield of Cr is 90-95%.
实施例2Example 2
在冶炼W75微碳钨铁时,炉料所用成分的含量百分及所用份额为:WO3为67.87%的钨精矿100份;硅为75%的硅铁粉21份;SiO2≥95%的硅石6份;CaF2≥85%的萤石2份,废钢屑4份。得到的钨铁成分为:W为75~77%,C为0.1~0.2%,Si≤0.5~1.0%,S<0.02%,P<0.02%;W的收得率为96~98%。When smelting W75 micro-carbon ferrotungsten, the content percentage and share of the ingredients used in the furnace charge are: 100 parts of tungsten concentrate with WO 3 being 67.87%; 21 parts of ferrosilicon powder with 75% silicon; SiO 2 ≥ 95% 6 parts of silica; 2 parts of fluorite with CaF 2 ≥ 85%; 4 parts of steel scrap. The obtained tungsten-iron composition is as follows: W is 75-77%, C is 0.1-0.2%, Si≤0.5-1.0%, S<0.02%, P<0.02%; W yield is 96-98%.
实施例3Example 3
在冶炼Mo60微碳钼铁时,炉料所用成分的含量百分及所用份额为:MoO3为69.82%的钼精矿100份;硅为75%的硅铁粉30份,CaO≥75%的石灰4份,CaF2≥85%的萤石1份,废钢屑15份。得到的钼铁成分为:Mo为60~62%,C为0.1~0.2%,S≤0.1~0.2%,P≤0.05~0.1%,Si≤1.0~1.5%;Mo的收得率为96~98%。When smelting Mo60 micro-carbon ferromolybdenum, the content percentage and share of the ingredients used in the charge are: 100 parts of molybdenum concentrate with MoO 3 being 69.82%; 30 parts of silicon ferrosilicon powder with 75% silicon, and lime with CaO≥75% 4 parts, 1 part of fluorspar with CaF 2 ≥ 85%, 15 parts of steel scrap. The obtained ferromolybdenum composition is: Mo is 60-62%, C is 0.1-0.2%, S≤0.1-0.2%, P≤0.05-0.1%, Si≤1.0-1.5%; the yield of Mo is 96~ 98%.
三相交流等离子熔融还原铬、钨、钼精矿直接冶炼微碳铁合金装置如图2所示。它包括等离子炉和等离子发生器两部分,等离子炉由炉盖「4」和炉体「5」两部分组成。炉盖「4」呈弧形,中心开有电极「2」、「8」、「9」插入和升降孔;炉体「5」为园台形,底部相应部位开有排渣口「6」和铁合金出口「7」,炉盖「4」和炉体「5」的炉壳用钢板焊结而成,均通水冷却,内砌高温耐火材料。The three-phase alternating current plasma smelting reduction chromium, tungsten, and molybdenum concentrate direct smelting micro-carbon ferroalloy device is shown in Figure 2. It includes two parts, a plasma furnace and a plasma generator, and the plasma furnace is composed of a furnace cover "4" and a furnace body "5". The furnace cover "4" is arc-shaped, with electrodes "2", "8" and "9" inserted and lifted holes in the center; The ferroalloy outlet "7", the furnace cover "4" and the furnace shell of the furnace body "5" are welded with steel plates, all cooled by water, and built with high-temperature refractories inside.
等离子发生器由三根沿轴心钻有小孔的石墨电极「2」、「8」、「9」组成,其中一根钻的孔径较大,兼供由喷粉罐「1」喷入炉料。水冷铜电极夹持器「3」供100~135V三相交流电输入,并与电极升降装置联接并绝缘,实现电极的升降、平移的工艺要求。The plasma generator is composed of three graphite electrodes "2", "8" and "9" with small holes drilled along the axis, one of which has a larger hole diameter, which is also used for spraying the charge from the powder spray tank "1". The water-cooled copper electrode holder "3" supplies 100-135V three-phase AC input, and is connected and insulated with the electrode lifting device to realize the technical requirements of the electrode's lifting and translation.
通过电极的小孔注入稳定流动的等离子载气体Ar或焦炉煤气,喷粉罐「1」用一定压力的Ar气作为气源,提供稳定流动的粉料喷入炉内。The stable flow of plasma carrier gas Ar or coke oven gas is injected through the small hole of the electrode, and the powder spray tank "1" uses a certain pressure of Ar gas as the gas source to provide stable flow of powder into the furnace.
本发明的具体操作是:提升电极「2」、「8」、「9」,开启炉盖「4」,先将配料所需的废钢屑、或废铁一次性加入炉内;再将经干燥、混匀并配料后的混合料加入炉内,装填到整个炉容的2/3左右,盖上炉盖「4」,插入电极「2」、「8」、「9」,启动水泵使炉盖「4」、炉壳「5」及水冷铜电极夹持器「3」通入冷却水。将剩余的混合粉料装入喷粉罐「1」,并用Ar气充压到一定压力;将电极「8」和「9」注入等离子载气,启动电源,引等离子弧,调节电极使等离子弧稳定。约5分钟后,待大部分炉料已熔融和还原,料面下降,上部空间已充满等离子气体。这时等离子弧已很稳定,开启喷粉罐下料球伐,向炉内供料,直至料喷完。调节电极「2」、「8」、「9」升降,进行埋弧精炼。冶炼结束,提升电极「2」、「8」、「9」,停电,停气,带渣出铁合金,最后出完全部炉渣。The specific operation of the present invention is: lift the electrodes "2", "8" and "9", open the furnace cover "4", first add scrap steel chips or scrap iron required for batching into the furnace at one time; , Mix and batch the mixture into the furnace, fill it to about 2/3 of the entire furnace capacity, cover the furnace cover "4", insert electrodes "2", "8", and "9", start the water pump to make the furnace The cover "4", the furnace shell "5" and the water-cooled copper electrode holder "3" are fed with cooling water. Put the remaining mixed powder into the powder spray tank "1", and pressurize it to a certain pressure with Ar gas; inject the electrodes "8" and "9" into the plasma carrier gas, start the power supply, start the plasma arc, and adjust the electrodes to make the plasma arc Stablize. After about 5 minutes, when most of the charge has been melted and reduced, the level of the charge has dropped, and the upper space has been filled with plasma gas. At this time, the plasma arc is very stable, and the powder spraying tank is opened to feed the ball and feed the material into the furnace until the material is sprayed. Adjust the lifting of electrodes "2", "8" and "9" for submerged arc refining. After the smelting is completed, the electrodes "2", "8", and "9" are lifted, the power is cut off, the gas is stopped, the ferroalloy is produced with slag, and finally all the slag is produced.
附表 schedule
Claims (10)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN99120078A CN1098935C (en) | 1999-11-24 | 1999-11-24 | AC plasma melting reduction process and equipment for direct smelting of ferroalloy with very low carbon content |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN99120078A CN1098935C (en) | 1999-11-24 | 1999-11-24 | AC plasma melting reduction process and equipment for direct smelting of ferroalloy with very low carbon content |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1298033A true CN1298033A (en) | 2001-06-06 |
| CN1098935C CN1098935C (en) | 2003-01-15 |
Family
ID=5281351
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN99120078A Expired - Fee Related CN1098935C (en) | 1999-11-24 | 1999-11-24 | AC plasma melting reduction process and equipment for direct smelting of ferroalloy with very low carbon content |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN1098935C (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103589867A (en) * | 2013-11-20 | 2014-02-19 | 北京环宇冠川等离子技术有限公司 | Method and device for treating ironmaking ash, mud and mill tailings by plasma torch heating technology |
| CN106591566A (en) * | 2016-12-12 | 2017-04-26 | 嵩县开拓者钼业有限公司 | Method for smelting tungsten-molybdenum-iron alloy from tungsten-molybdenum associated mineral |
| CN106636857A (en) * | 2016-09-29 | 2017-05-10 | 成都真火科技有限公司 | Alloy steel smelting method |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AT375404B (en) * | 1983-02-03 | 1984-08-10 | Voest Alpine Ag | METHOD FOR CARRYING OUT MELTING, MELTING METALURGICAL AND / OR REDUCTION METALURGICAL PROCESSES IN A PLASMA MELTING FURNACE AND DEVICE FOR CARRYING OUT THE METHOD |
| US4731112A (en) * | 1986-02-19 | 1988-03-15 | Midrex International, B.V. Rotterdam, Zurich Branch | Method of producing ferro-alloys |
| CN1051579C (en) * | 1996-09-18 | 2000-04-19 | 中国科学院力学研究所 | Method and apparatus for smelting high melting metal by plasma |
-
1999
- 1999-11-24 CN CN99120078A patent/CN1098935C/en not_active Expired - Fee Related
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103589867A (en) * | 2013-11-20 | 2014-02-19 | 北京环宇冠川等离子技术有限公司 | Method and device for treating ironmaking ash, mud and mill tailings by plasma torch heating technology |
| CN106636857A (en) * | 2016-09-29 | 2017-05-10 | 成都真火科技有限公司 | Alloy steel smelting method |
| CN106636857B (en) * | 2016-09-29 | 2018-05-11 | 成都真火科技有限公司 | A kind of smelting process of steel alloy |
| CN106591566A (en) * | 2016-12-12 | 2017-04-26 | 嵩县开拓者钼业有限公司 | Method for smelting tungsten-molybdenum-iron alloy from tungsten-molybdenum associated mineral |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1098935C (en) | 2003-01-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR100364934B1 (en) | Method of making iron and steel | |
| CN103469049B (en) | Molybdenum oxide DIRECT ALLOYING process for making | |
| EP2210959B1 (en) | Process for producing molten iron | |
| CN107326150B (en) | A kind of production method of full steel scrap electric arc furnaces duplex Clean Steel Smelting | |
| CN101890594A (en) | Low hydrogen basic electrode for welding 25Cr2Ni4MoV alloy steel | |
| CN101177755A (en) | A method for smelting high-speed steel using oxide ore | |
| CN114015831B (en) | Smelting method for improving end point carbon of high-carbon steel of electric furnace | |
| CN113249639A (en) | Production method for improving castability of silicon-manganese killed silicon steel | |
| CN112595093A (en) | Electrode heating process and device capable of blowing powder for electric arc furnace | |
| CN117230273A (en) | Method for smelting low-nitrogen steel by adopting electric arc furnace | |
| CN115595493B (en) | A method for smelting low-phosphorus high-manganese steel based on ferromanganese reduction dephosphorization | |
| CN100363508C (en) | Electric furnace to converter steel making production process | |
| CN1312307C (en) | Mangan-alloy production | |
| CN101386950A (en) | Ferronickel intermediate alloy and smelting purification treatment method thereof | |
| CN1098935C (en) | AC plasma melting reduction process and equipment for direct smelting of ferroalloy with very low carbon content | |
| CN1295134A (en) | Direct stainless steel smelting method and smelter by AC plasma melting to reduce concentrated nichromite | |
| CN1255558C (en) | Production technology for melting steel by electric arc furnace converter | |
| KR102628195B1 (en) | Molten steel manufacturing method | |
| US2557458A (en) | Method of fusing alloy additions to a steel bath | |
| US4913732A (en) | Method for smelting reduction in electric furnace | |
| CN109971974B (en) | Production process for refining blister copper | |
| CN1497054A (en) | Refining method of molten metal containing chromium | |
| RU2092573C1 (en) | Charge preparation for metallurgical refining process | |
| Dutta et al. | Electric Furnace Processes | |
| RU2302471C1 (en) | Method of making steel in electric arc steel melting furnace |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C06 | Publication | ||
| PB01 | Publication | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| C19 | Lapse of patent right due to non-payment of the annual fee | ||
| CF01 | Termination of patent right due to non-payment of annual fee |