CN1070237C - Process for making acidic spheroidized ore - Google Patents
Process for making acidic spheroidized ore Download PDFInfo
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- CN1070237C CN1070237C CN99115416A CN99115416A CN1070237C CN 1070237 C CN1070237 C CN 1070237C CN 99115416 A CN99115416 A CN 99115416A CN 99115416 A CN99115416 A CN 99115416A CN 1070237 C CN1070237 C CN 1070237C
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- ore
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- spheroidized
- acidic
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- 238000000034 method Methods 0.000 title claims abstract description 13
- 230000002378 acidificating effect Effects 0.000 title claims abstract description 9
- 230000008569 process Effects 0.000 title claims abstract description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 18
- 239000003245 coal Substances 0.000 claims abstract description 13
- 239000000843 powder Substances 0.000 claims abstract description 12
- 239000000446 fuel Substances 0.000 claims abstract description 9
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 claims abstract description 8
- 229910052742 iron Inorganic materials 0.000 claims abstract description 8
- 239000012141 concentrate Substances 0.000 claims abstract description 6
- 239000000463 material Substances 0.000 claims abstract description 6
- 230000007246 mechanism Effects 0.000 claims abstract description 6
- 239000011230 binding agent Substances 0.000 claims abstract description 5
- 239000002994 raw material Substances 0.000 claims abstract description 5
- 239000007788 liquid Substances 0.000 claims abstract description 4
- 239000008188 pellet Substances 0.000 claims description 27
- 238000001035 drying Methods 0.000 claims description 9
- 238000007596 consolidation process Methods 0.000 claims description 7
- 238000005453 pelletization Methods 0.000 claims description 6
- 229910004298 SiO 2 Inorganic materials 0.000 claims description 3
- 239000004449 solid propellant Substances 0.000 claims description 3
- 239000002912 waste gas Substances 0.000 claims description 3
- 238000001816 cooling Methods 0.000 claims description 2
- 239000007789 gas Substances 0.000 claims description 2
- 238000012216 screening Methods 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims 4
- 239000002817 coal dust Substances 0.000 claims 3
- 238000013467 fragmentation Methods 0.000 claims 1
- 238000006062 fragmentation reaction Methods 0.000 claims 1
- 238000005245 sintering Methods 0.000 abstract description 10
- 230000009467 reduction Effects 0.000 abstract description 8
- 238000005265 energy consumption Methods 0.000 abstract description 6
- 229910000278 bentonite Inorganic materials 0.000 abstract description 5
- 239000000440 bentonite Substances 0.000 abstract description 5
- 238000002485 combustion reaction Methods 0.000 abstract description 4
- 239000007787 solid Substances 0.000 abstract description 3
- 230000015556 catabolic process Effects 0.000 abstract 1
- 238000006731 degradation reaction Methods 0.000 abstract 1
- 239000002253 acid Substances 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 7
- 238000009792 diffusion process Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000007790 solid phase Substances 0.000 description 3
- RHZUVFJBSILHOK-UHFFFAOYSA-N anthracen-1-ylmethanolate Chemical compound C1=CC=C2C=C3C(C[O-])=CC=CC3=CC2=C1 RHZUVFJBSILHOK-UHFFFAOYSA-N 0.000 description 2
- 239000003830 anthracite Substances 0.000 description 2
- 238000003723 Smelting Methods 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 229910052840 fayalite Inorganic materials 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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- Manufacture And Refinement Of Metals (AREA)
Abstract
Description
本发明涉及一种高炉炼铁原料的制造方法。The invention relates to a method for manufacturing blast furnace ironmaking raw materials.
目前国内外常规的高炉炼铁原料可分为酸性球团矿和烧结矿,酸性球团矿生产方法可分为竖炉球团法、带式机焙烧法、链箅机——回转窑法三大类,通常以气体燃料或液体燃料燃烧提供球团焙烧所需热源,国内也有部分生产厂家使用固体燃料煤粉燃烧,用于竖炉球团焙烧法,但煤粉的燃烧在炉外进行,上述几种方法的固结机理为固相扩散粘结,具有材质要求高,投资大,生产成本高,窑内易结圈的缺点。中国专利申请(申请号98102028)提出一种用烧结机生产酸性球团烧结矿的方法,其固结机理是靠铁酸钙液相(高碱度)或铁橄榄石液相和玻璃质(酸性炉料)粘结成烧结矿,但所生成的烧结矿还原性差,强度差,品位低,不利于强化高炉冶炼。At present, the conventional blast furnace ironmaking raw materials at home and abroad can be divided into acid pellets and sintered ore, and the production methods of acid pellets can be divided into shaft furnace pellet method, belt machine roasting method, chain grate machine-rotary kiln method three Generally, gas fuel or liquid fuel is used to provide the heat source required for pellet roasting. Some domestic manufacturers also use solid fuel coal powder combustion for the shaft furnace pellet roasting method, but the combustion of coal powder is carried out outside the furnace. The consolidation mechanism of the above methods is solid phase diffusion bonding, which has the disadvantages of high material requirements, large investment, high production cost, and easy ring formation in the kiln. Chinese patent application (application number 98102028) proposes a method for producing acidic pellet sintered ore with a sintering machine. charge) bonded into sinter, but the generated sinter has poor reducibility, poor strength, and low grade, which is not conducive to strengthening blast furnace smelting.
为了解决以上不足,本发明提供一种利用酸性球团矿固结机理、采用烧结机生产酸性球团矿的方法。In order to solve the above deficiencies, the present invention provides a method for producing acid pellets by utilizing the consolidation mechanism of acid pellets and using a sintering machine.
本发明以高品位铁精矿(TFe63~66%,SiO2<5.5%)为原料,添加膨润土做粘结剂,采用煤粉直接配入料层燃烧,利用酸性球团矿固结机理,采用烧结机生产酸性球团矿,包括配料、造球、干燥、点火、焙烧、破碎、筛分等过程,具体工艺过程如下:The invention uses high-grade iron ore concentrate (TFe63~66%, SiO 2 <5.5%) as raw material, adds bentonite as binder, adopts coal powder to directly blend into the material layer for combustion, utilizes the consolidation mechanism of acidic pellets, adopts The sintering machine produces acid pellets, including batching, pelletizing, drying, ignition, roasting, crushing, screening and other processes. The specific process is as follows:
a>使用膨润土做粘结剂,强化造球和球团焙烧,膨润土配比1.0~2.0%(重量百分比,以下同),使用固体燃料煤粉替代气体燃料或液体燃料,煤粉配比为3.5~4.5%(重量百分比)(粒度<3mm),其中造球时内配煤粉配比为1.2~1.5%。a> Use bentonite as binder, strengthen pelletizing and pellet roasting, the ratio of bentonite is 1.0-2.0% (percentage by weight, the same below), use solid fuel pulverized coal instead of gaseous fuel or liquid fuel, and the ratio of pulverized coal is 3.5 ~4.5% (weight percentage) (particle size<3mm), wherein the proportion of internally blended coal powder is 1.2-1.5% during pelletizing.
b>造球后外配煤粉配比为2.3~3.0%,以降低生产成本,采用园盘造球机造球,然后在园筒混合机中将煤粉与球团混匀,以控制料层中煤粉燃烧速度。b> After pelletizing, the ratio of external coal powder is 2.3-3.0%. Burning speed of pulverized coal in the layer.
c>生球粒度控制5~15mm≥80%,生球水分7.5~10%,生球抗压强度≥10牛/个,生球落下强度≥4.5次/0.5米。c>The particle size of green balls should be 5-15 mm ≥ 80%, the water content of green balls should be 7.5-10%, the compressive strength of green balls should be ≥ 10 N/piece, and the drop strength of green balls should be ≥ 4.5 times/0.5 meters.
d>料层高度为500~700mm,在点火焙烧前设置干燥段,干燥时间占焙烧时间的5~20%,干燥温度200~300℃,以球团矿冷却废气或点火器废气为热源。d>The height of the material layer is 500-700mm, and the drying section is set before ignition and roasting. The drying time accounts for 5-20% of the roasting time, and the drying temperature is 200-300°C. The pellet cooling waste gas or igniter waste gas is used as the heat source.
e>点火时间1~2min,点火温度1150±50℃,点火负压4000~6000Pa,焙烧负压8000~10000Pa,垂直焙烧速度控制在15~20mm/min。e>Ignition time 1-2min, ignition temperature 1150±50°C, ignition negative pressure 4000-6000Pa, roasting negative pressure 8000-10000Pa, vertical roasting speed controlled at 15-20mm/min.
本发明利用酸性球团矿固结机理,确保酸性球团矿的固相扩散固结。球团矿以Fe3O4或Fe2O3再结晶的固相扩散固结为主,玻璃质仅占4~5%,极少量铁橄榄石。具有如下的优点:1.适于中小厂进行技术改造,改善高炉炉料结构,投资省,见效快,改造旧烧结机即可,容易推广,节省投资85%左右;2.产量高、能耗低,烧结机焙烧酸性球团矿时利用系数为1.5~1.7t/m2·h,固体能耗50Kg/t·p,而带式焙烧机利用系数仅0.8~1.0t/m2·h,燃料消耗为50Kg/t·P,即带式烧结机焙烧酸性球团产量提高一倍,而能耗相当;3.球团矿铁品位高(TFe>60%),强度高(ISO转鼓强度≥70%),还原性好(RI>55%),低温还原粉化率低(RDI+3.15≥75%),900℃还原后强度好(-3.15mm<20%)。The invention utilizes the consolidation mechanism of the acid pellets to ensure the solid phase diffusion and consolidation of the acid pellets. The pellets are mainly composed of solid phase diffusion and consolidation of Fe 3 O 4 or Fe 2 O 3 recrystallization, glass only accounts for 4-5%, and a very small amount of fayalite. It has the following advantages: 1. It is suitable for small and medium-sized factories to carry out technological transformation, improve the structure of blast furnace charge, save investment, and have quick results. It is only necessary to transform the old sintering machine, easy to promote, and save about 85% of investment; 2. High output and low energy consumption, the utilization coefficient of sintering machine roasting acid pellets is 1.5~1.7t/m 2 h, the solid energy consumption is 50Kg/t·p, while the utilization coefficient of belt roaster is only 0.8~1.0t/ m 2 ·h, the fuel consumption is 50Kg/t·P, that is to say, the production of acid pellets roasted by the belt sintering machine is doubled, while the energy consumption is equal; 3. Pellet ore has high iron grade (TFe>60%), high strength (ISO drum strength≥70%), good reducibility (RI>55%), low low-temperature reduction pulverization rate (RDI +3.15 ≥75%), Good strength after reduction at 900°C (-3.15mm<20%).
附图说明:Description of drawings:
图1:本发明工艺流程图。Fig. 1: Process flow chart of the present invention.
实施例:Example:
1.铁精矿(TFe 65.38%,SiO24.8 3%)再配入1%的膨润土和2%的无烟煤粉(-1mm占88.68%)及20%返矿混匀后,在Φ1m园盘造球机上造球,生球粒度5~15mm≥80%,生球水分8.5%,生球与2.5%的无烟煤粉在园筒混合机中混匀3min,然后在Φ250mm烧结杯中干燥2min(干燥温度250℃,干燥负压5000Pa),点火2min(点火温度1150±50℃,点火负压4000Pa),焙烧负压8000Pa,料层高度700mm,垂直焙烧速度控制在14~20mm/min,在上述条件下,烧结机上球团矿产量(利用系数)达1.67t/m2·h,球团矿转鼓强度(ISO)≥70%,成品率70~80%,固体能耗55~60Kg/t·p,球团矿品位TFe 62.83%,FeO10~13%,还原性(RI)55~68%,低温还原粉率RDI+3.1580%,900℃还原后强度-3.15mm为20%。1. Iron concentrate (TFe 65.38%, SiO 2 4.8 3%) is mixed with 1% bentonite and 2% anthracite powder (-1mm accounts for 88.68%) and 20% returned ore, and then mixed on the Φ1m disc pelletizer For pelletizing, the particle size of green pellets is 5-15mm≥80%, the moisture content of green pellets is 8.5%, and the raw pellets are mixed with 2.5% anthracite coal powder in a cylinder mixer for 3 minutes, and then dried in a Φ250mm sintering cup for 2 minutes (drying temperature 250°C , drying negative pressure 5000Pa), ignition for 2min (ignition temperature 1150±50°C, ignition negative pressure 4000Pa), roasting negative pressure 8000Pa, material layer height 700mm, vertical roasting speed controlled at 14-20mm/min, under the above conditions, sintering On-board pellet production (utilization coefficient) reaches 1.67t/m 2 h, drum strength of pellets (ISO) ≥ 70%, finished product rate 70-80%, solid energy consumption 55-60Kg/t·p, pellets Agglomerate grade TFe 62.83%, FeO 10-13%, reduction (RI) 55-68%, low-temperature reduction powder rate RDI +3.15 80%, strength after reduction at 900°C -3.15mm is 20%.
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CN99115416A CN1070237C (en) | 1999-06-14 | 1999-06-14 | Process for making acidic spheroidized ore |
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CN99115416A CN1070237C (en) | 1999-06-14 | 1999-06-14 | Process for making acidic spheroidized ore |
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CN1070237C true CN1070237C (en) | 2001-08-29 |
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CN103436693B (en) * | 2013-08-15 | 2015-04-22 | 内蒙古包钢钢联股份有限公司 | Pellet with high FeO content and preparation method of pellet |
CN104263913A (en) * | 2014-09-27 | 2015-01-07 | 武钢集团昆明钢铁股份有限公司 | Preparation method for acidic hemispherical sinters |
CN104911338B (en) * | 2015-04-28 | 2017-06-30 | 攀钢集团攀枝花钢铁研究院有限公司 | A kind of raw materials for sintering composition and acid vanadium titanium sintering deposit and its preparation method and application |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
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JPS55154534A (en) * | 1979-04-12 | 1980-12-02 | Kobe Steel Ltd | Iron ore porous pellet and its manufacture |
CN1201835A (en) * | 1998-05-29 | 1998-12-16 | 冶金工业部钢铁研究总院 | Production of sintered pelletized minerals |
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Publication number | Priority date | Publication date | Assignee | Title |
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JPS55154534A (en) * | 1979-04-12 | 1980-12-02 | Kobe Steel Ltd | Iron ore porous pellet and its manufacture |
CN1201835A (en) * | 1998-05-29 | 1998-12-16 | 冶金工业部钢铁研究总院 | Production of sintered pelletized minerals |
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