CN1005276B - 精炼熔融金属的方法 - Google Patents
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- 229910052751 metal Inorganic materials 0.000 title claims abstract description 52
- 239000002184 metal Substances 0.000 title claims abstract description 52
- 238000000034 method Methods 0.000 title claims abstract description 35
- 238000007670 refining Methods 0.000 title claims abstract description 31
- 229910052698 phosphorus Inorganic materials 0.000 claims abstract description 31
- 239000011574 phosphorus Substances 0.000 claims abstract description 31
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims abstract description 30
- 229910000831 Steel Inorganic materials 0.000 claims abstract description 28
- 239000010959 steel Substances 0.000 claims abstract description 28
- 239000002893 slag Substances 0.000 claims abstract description 25
- 239000007789 gas Substances 0.000 claims abstract description 20
- 235000008733 Citrus aurantifolia Nutrition 0.000 claims abstract description 13
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims abstract description 13
- 235000011941 Tilia x europaea Nutrition 0.000 claims abstract description 13
- 239000004571 lime Substances 0.000 claims abstract description 13
- 229910052748 manganese Inorganic materials 0.000 claims abstract description 13
- 239000011572 manganese Substances 0.000 claims abstract description 13
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims abstract description 7
- 238000005261 decarburization Methods 0.000 claims abstract description 4
- 238000004519 manufacturing process Methods 0.000 claims abstract description 3
- 238000007664 blowing Methods 0.000 claims description 13
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 5
- 229910052710 silicon Inorganic materials 0.000 claims description 5
- 239000010703 silicon Substances 0.000 claims description 5
- 229910001341 Crude steel Inorganic materials 0.000 claims 1
- 238000003756 stirring Methods 0.000 abstract description 8
- 239000000155 melt Substances 0.000 abstract 2
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 abstract 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 20
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 9
- 229910052799 carbon Inorganic materials 0.000 description 9
- 229910052742 iron Inorganic materials 0.000 description 9
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 8
- 239000001301 oxygen Substances 0.000 description 8
- 229910052760 oxygen Inorganic materials 0.000 description 8
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 7
- 239000005864 Sulphur Substances 0.000 description 7
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 6
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 6
- 238000012856 packing Methods 0.000 description 6
- 238000003723 Smelting Methods 0.000 description 3
- 229910052786 argon Inorganic materials 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 238000007599 discharging Methods 0.000 description 2
- 239000010436 fluorite Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 229910000617 Mangalloy Inorganic materials 0.000 description 1
- 238000005275 alloying Methods 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- -1 by weight Substances 0.000 description 1
- 235000011089 carbon dioxide Nutrition 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 239000012159 carrier gas Substances 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- NDLPOXTZKUMGOV-UHFFFAOYSA-N oxo(oxoferriooxy)iron hydrate Chemical compound O.O=[Fe]O[Fe]=O NDLPOXTZKUMGOV-UHFFFAOYSA-N 0.000 description 1
- 150000003017 phosphorus Chemical class 0.000 description 1
- 239000011819 refractory material Substances 0.000 description 1
- 239000003923 scrap metal Substances 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21C—PROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
- C21C7/00—Treating molten ferrous alloys, e.g. steel, not covered by groups C21C1/00 - C21C5/00
- C21C7/04—Removing impurities by adding a treating agent
- C21C7/064—Dephosphorising; Desulfurising
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21C—PROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
- C21C5/00—Manufacture of carbon-steel, e.g. plain mild steel, medium carbon steel or cast steel or stainless steel
- C21C5/28—Manufacture of steel in the converter
- C21C5/30—Regulating or controlling the blowing
- C21C5/32—Blowing from above
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- Treatment Of Steel In Its Molten State (AREA)
- Refinement Of Pig-Iron, Manufacture Of Cast Iron, And Steel Manufacture Other Than In Revolving Furnaces (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
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Abstract
本发明阐述从常见磷含量的熔融金属,生产低磷钢的方法。采用这种方法,在冶金炉中,尤其是转炉里的熔融金属,可以一步同时完成脱碳和脱磷。炼制中,主要或完全由工业级纯氧组成的炼制气顶吹到熔融液,并把惰性搅拌气体,从下面吹入熔融液。炉内装有的熔融金属的含锰量,按重量计,低于0.2%,随后加入石灰进行精炼。吹炼结束时,钢水里最终含磷量,按重量计,可降到0.005%或更低,而不更换炉渣。
Description
本发明阐述从常见的磷含量的熔融生产低磷钢的方法。采用这种方法,在冶金炉中,尤其是在转炉里的熔融金属,可以一步同时完成脱碳和脱磷。炼制中,主要或完全由工业级纯氧组成的炼制气体顶吹到熔融液上,并吹入某种惰性搅拌气体。
众所周知,磷对钢的性能起着不良影响。除某些钢种,故意加进磷作合金元素意外,大多数钢种要求其中磷含量,按重量计,低至0.010到0.030%。由上述大家知道的吹炼方法,可达到该磷含量。
西德专利3,318,332发现了一种进一步降低磷含量的方法,这种方法是在转炉里装入脱硅的熔融金属,由炉顶吹入炼制用的氧,并连同往熔融金属加入成渣剂,同时从熔体下面吹入由惰性气体、氮、氧、一氧化碳,二氧化碳或其混合物组成的气体。用这种精炼方法,其指标是,最后磷含量,按重计,等于和低于0.010%。
这种方法的缺点是,熔融金属温度下降很多,并产生额外量的炉渣,这些沪渣必须转去另外再处理,同时,还增加了铁的损耗和耐火材料的消耗。
按照西德专利2,842,563告知的方法,在常规的炼制过程结束或即将结束之前,也就是说,当钢水中碳含量,按重量计,已低于0.4%,此时,精炉渣也已大量除去,便将CaCO3和Na2CO3,按1∶1的比例,放进精炼炉中沸腾钢水中,同时加入萤石和/或氧化铁,每种用量多到碳酸盐混合物重量的30%,通过往钢水里通入载气,其通入深度能使所有的炉渣彻底混合,然后放出钢水,同时挡住熔炼的炉渣,在钢水包中按原先知道的方法完工。用这种方法,据说,钢中的磷含量可降到低于0.001%。
在西德专利3,245,098告知的另一种方法中,转炉里的钢水不脱磷,或只是在脱碳以后微脱一下磷,便流到一个能够加热的钢水包中,流出温度主要在碳燃烧后确定,然后,在钢水包里,按原先知道的方法,吹入脱磷剂。
这两种大家知道的方法的缺点,仍然是产生多量的炉渣,这些炉渣必须用昂贵的方法重新处理或运往垃圾场。此外,由于加入成渣剂,又使温度下降,妨碍了加入废金属。
本发明目的是,以兼有吹炼-精炼的一步冶炼法,使熔融金属里常见的磷含量(按重量计算,一般达到0.2%),降到低于0.005%(按重量计),而不必有额外的费用。
从本文开始所述的一般类型的方法出发,按照本发明,当炉内装的熔融金属含磷量,按重量计,低于0.2%,而且炼制进行到钢中的最终磷含量,按重量计,降到0.005%或更少,本发明的目标便可达到。
在大家知道的复合吹炼法中,氧气由炉顶吹入,搅拌气体由下面吹入,所用熔融金属的锰含量,按重量计,一般约为0.4%-0.8%,例见西德杂志“Stahl und Eisen”,104(1984),第16,767-773页。第769页上的图6,表示所用熔融金属的锰含量约为0.50%-0.60%。精炼后的钢水最后磷含量,同转炉大小有关,其范围为0.010%至0.020%,例见西德杂志“Stahl und Eisen”,103,(1983),第4,769-771页的图4,9,和12 163-165页关于另一种复合吹炼法,熔融金属中平均含锰量1.29%,便被说成是很低的(第165页,左栏,第一段,以及图5),不过,在这个刊物里,没有发现有炼制钢的最终磷含量。
本发明现在是基于这样的发现即当所用熔融金属锰含量,按重量计,低于0.2%,精炼后钢水的最后磷含量,按重量计,能低至0.005%。或更少。这就使消除大家知道的方法所固有的缺点成为可能。
在专家中迄今流行这样的看法,即所用熔融金属的锰含量,按重量计,数量级必须达0.4%到0.8%,才能实施这类吹炼方法。熔融金属中的这些锰含量,是要防止在吹炼完毕的炉渣里含铁量达多,以至平均数超过20%。而按照本发明,由于熔融金属的锰含量,按重量计,限于0.2%,然而加入的石灰能出乎意料地被活化,由于炼制早期的铁氧化而得到促进,这就加速了熔融金属里磷的氧化,生成的(P2O5),可以在炼制早期,就以稳定的形式固定在炉渣里。
低锰含量的熔融金属原料可以不难获得,也不需由于高炉中使用廉价的低锰含量矿和由于省去了再次使用高炉原料中的含锰钢厂炉渣所需的费用。
用一步工艺,即可炼制得到低的含磷量的钢,这是本发明方法的突出优点。这意味着,没有必要单独的预先脱磷。
按照本发明的某推荐实例,如果采用含硅重量为0.15%到0.35%最好少于0.3%的熔融金属,与降低所需石灰量有关的一个优点是所得到的炉渣量。石灰量达到每吨熔融金属需20到40公斤。在所述范围里,较低的石灰相应于较低的硅含量。
这样,由高炉法得到的硅,锰含量低的熔融金属,可以立即用一步吹炼法炼制,无需在前面先脱磷,也无需更换炉渣以降低碳、硫,特别是磷的含量。
在冶金炉中,尤其是在转炉中采用这种方法,工业纯氧经炉顶的吹管,吹入熔融金属液。同时,某种惰性搅拌气体由下面吹入熔融液。从顶吹氧气开始后就持续地或间歇地这样做直到精炼好的钢水出料。在间歇吹的情况下,尤其是在炼制开始和后期的占总的吹气时间30%的吹炼时间里,必须吹入惰性搅拌气体。
参考下面实例,对本发明作更详细的说明。
例1
330吨熔融金属,其组成为:(按重量计算)
4.60%碳 0.08%磷
0.17%锰 0.018%硫
0.35%硅 其余为铁
将它们装入温度为1,344℃的转炉里,同时装入96吨废钢。精炼气体仍然是工业纯氧,它由炉顶吹入熔融金属。每吨熔融金属的石灰加入量为51公斤。
从开始顶吹氧气到炼制好的钢水放料,用作搅拌气体的氩气,从下面吹入熔融金属,其吹入速度为平均每吨炼制金属每分钟0.03立方米(S.T.P)。吹炼结束时,温度是1640℃。此时取出的样品有下列组成:(按重量计算)
0.029%碳 0.005%磷
0.07%锰 0.010%硫
其余为铁
每吨熔融金属的炉渣量为99公斤,炉渣的含铁量Fe-16.9%(按重量计)。
例2
316吨熔融金属,其组成为:(按重量计算)
4.68%碳 0.08%磷
0.16%锰 0.019%硫
0.24%硅 其余为铁
将它们装入温度为1300℃的转炉里,同时装入95吨废钢。
所用的炼制用气体仍然是工业纯氧气,它由炉顶吹入熔融金属。每吨熔融金属的石灰加入量为31公斤。
从氧气顶吹开始到结束,用作搅拌气体的氩气由下面吹入熔融金属,其速度为平均每吨熔融金属每分钟0.03立方米(S.T.P)。吹炼结束时,熔融金属温度是1630℃。此时取出的样品有下列组成:(按重量计算)
0.025%碳 0.004%磷
0.08%锰 0.017%硫
其余为铁
每吨熔融金属的炉渣量为79公斤,炉渣的含铁量Fe-17.9%(按重量计)。
例3
没有被本发明包括在内的这个比较例,用了305吨熔融金属,其组成为:(按重量计)
4.60%碳 0.10%磷
0.61%锰 0.019%硫
其余为铁
它同105吨废钢一起装入1340℃的转炉。
所用的炼制用气是工业纯氧,它由炉顶吹入熔融金属。每吨熔融金属的石灰加入量为54公斤。
从氧气顶吹氧气到冶炼好的钢水出料,用作搅拌气体的氩气,由下面吹入熔融金属,其速度为平均每吨熔融金属每分钟0.03立方米(S.T.P)。持续时间为18分钟。吹炼结束时,熔融金属温度是1.625℃。此时取出的样品有下列组成:(按重量计算)
0.026%碳 0.011%磷
0.22%锰 0.011%硫
其余为铁
每吨熔融金属的炉渣量为111公斤,炉渣的含铁量Fe-18.50%(按重量计)。
将比较例结果同根据本发明的例1、例2相对照,可以看到,在起始含磷量大致相同情况下,当转炉里装入的熔融金属的锰含量,按重量计,低于0.20%,炼制好的钢里的磷含量,按重量计,能降低到0.005%和更低。同时,并不会增加铁的成渣,或出现其它方法的缺点。另外,如果降低熔融金属的硅含量,石灰用量可进一步降低(见例2),这样,也减少的生成的炉渣量。优于比较例的另一优点是,实施这种吹炼方法,钢水不会沸腾。这就很大程度上消除了大家知道的炉渣和钢水喷射。
本发明方法适用于精炼含磷量低的熔融金属,其初始含磷量,按重量计,从0.02至0.2%,最好是在0.15%以下。
吹炼开始时,加入的石灰呈块状(8-40毫米)。当按本发明方法实施吹炼时,石灰加入量主要取决于含硅量,其用量不会超过不照本发明方法实施的一般类型冶炼的用量。
吹炼结束时的炉内温度,应不超过1,650℃
按照本发明方法,炉渣里不加诸如萤石或矾土等助溶剂。
Claims (2)
1、在冶金炉,特别是在转炉中使通常含磷量的熔融金属同时脱碳,脱磷而生产低磷钢的方法,炼制中,由炉顶往熔融金属液里吹入主要或完全由工业级纯氧组成的炼制气体,并把惰性搅拌气体吹入熔融金属,特别是从下面吹入,其特征在于,炉内装有的熔融金属含锰量,按重量计,低于0.2%,随后加入石灰,炼制一直进行到在吹炼结束时钢水里最终含磷量,按重量计,可降到0.005%或更低,而不更换炉渣。
2、根据权利要求1的方法,其特征在于所用熔融金属的含硅量,按重计,为0.15至0.35%,在精炼中,每吨粗钢加入20至40分斤石灰。
Priority Applications (15)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE3434894A DE3434894C2 (de) | 1984-09-22 | 1984-09-22 | Verfahren zum Frischen von Roheisen |
DE8585110495T DE3567031D1 (en) | 1984-09-22 | 1985-08-21 | Process for refining pig iron |
AT85110495T ATE39497T1 (de) | 1984-09-22 | 1985-08-21 | Verfahren zum frischen von roheisen. |
EP85110495A EP0175924B1 (de) | 1984-09-22 | 1985-08-21 | Verfahren zum Frischen von Roheisen |
AU46540/85A AU569412B2 (en) | 1984-09-22 | 1985-08-22 | Conversion of low-manganese molten iron to low-phosphorus molten steel |
FI853294A FI77694C (fi) | 1984-09-22 | 1985-08-28 | Foerfarande foer framstaellning av staol med laog fosforhalt. |
ZA856561A ZA856561B (en) | 1984-09-22 | 1985-08-28 | Process for refining hot metal |
ES546700A ES8703936A1 (es) | 1984-09-22 | 1985-09-04 | Proceso para afino de arrabio |
MX8889A MX164702B (es) | 1984-09-22 | 1985-09-05 | Procedimiento para refinar metal caliente |
US06/774,632 US4604138A (en) | 1984-09-22 | 1985-09-11 | Process for refining hot metal |
CN85106853.7A CN1005276B (zh) | 1984-09-22 | 1985-09-12 | 精炼熔融金属的方法 |
JP60201953A JPS6179709A (ja) | 1984-09-22 | 1985-09-13 | 鋼の製造方法 |
IN655/CAL/85A IN163954B (zh) | 1984-09-22 | 1985-09-16 | |
CA000491216A CA1234989A (en) | 1984-09-22 | 1985-09-20 | Process for refining hot metal |
BR8504605A BR8504605A (pt) | 1984-09-22 | 1985-09-20 | Processo para a producao de aco de baixo teor de fosforo a partir de metal quente tendo teor usual de fosforo |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE3434894A DE3434894C2 (de) | 1984-09-22 | 1984-09-22 | Verfahren zum Frischen von Roheisen |
CN85106853.7A CN1005276B (zh) | 1984-09-22 | 1985-09-12 | 精炼熔融金属的方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN85106853A CN85106853A (zh) | 1987-03-11 |
CN1005276B true CN1005276B (zh) | 1989-09-27 |
Family
ID=25742039
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN85106853.7A Expired CN1005276B (zh) | 1984-09-22 | 1985-09-12 | 精炼熔融金属的方法 |
Country Status (14)
Country | Link |
---|---|
US (1) | US4604138A (zh) |
EP (1) | EP0175924B1 (zh) |
JP (1) | JPS6179709A (zh) |
CN (1) | CN1005276B (zh) |
AT (1) | ATE39497T1 (zh) |
AU (1) | AU569412B2 (zh) |
BR (1) | BR8504605A (zh) |
CA (1) | CA1234989A (zh) |
DE (2) | DE3434894C2 (zh) |
ES (1) | ES8703936A1 (zh) |
FI (1) | FI77694C (zh) |
IN (1) | IN163954B (zh) |
MX (1) | MX164702B (zh) |
ZA (1) | ZA856561B (zh) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN100351399C (zh) * | 2001-02-07 | 2007-11-28 | 新日本制铁株式会社 | 生铁熔体脱磷的方法 |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3707696A1 (de) * | 1987-03-11 | 1988-09-22 | Thyssen Stahl Ag | Verfahren zur herstellung von ferromangan affine |
DE3931024C1 (en) * | 1989-09-16 | 1991-05-16 | Krupp Stahl Ag, 4630 Bochum, De | Steel prodn. having low phosphor content - comprises single stage process using calcium oxide saturated residual stage from porous melt |
DE10215839A1 (de) * | 2002-04-10 | 2003-11-06 | Sms Demag Ag | Verfahren und Einrichtung zum Erzeugen von C-Stählen oder nichtrostenden Stählen durch Frischen von phosphorreichem Roheisen im Elektrolichtbogen-Ofen oder im Konverter-Gefäß |
CN101007340B (zh) * | 2007-01-25 | 2010-05-19 | 鞍钢股份有限公司 | 连铸中间包减少浇余钢水的处理方法 |
JP5471151B2 (ja) * | 2009-08-18 | 2014-04-16 | Jfeスチール株式会社 | 転炉製鋼方法 |
JP2013133536A (ja) * | 2011-12-27 | 2013-07-08 | Jfe Steel Corp | 溶鋼の製造方法 |
CN113106321A (zh) * | 2021-03-16 | 2021-07-13 | 首钢集团有限公司 | 一种新型含硅超低碳钢的生产制造方法 |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3714042A (en) * | 1969-03-27 | 1973-01-30 | Lubrizol Corp | Treated overbased complexes |
US3813337A (en) * | 1971-03-18 | 1974-05-28 | Atlantic Richfield Co | Metal working lubricant composition |
BE789599A (fr) * | 1971-10-01 | 1973-02-01 | Resch Werner | Procede d'affinage de fonte brute riche en phosphore |
US3929650A (en) * | 1974-03-22 | 1975-12-30 | Chevron Res | Extreme pressure agent and its preparation |
US4119549A (en) * | 1975-03-21 | 1978-10-10 | The Lubrizol Corporation | Sulfurized compositions |
US4116873A (en) * | 1975-06-09 | 1978-09-26 | Chevron Research Company | Lubricating oil composition containing Group I or Group II metal or lead sulfonates |
US4326972A (en) * | 1978-06-14 | 1982-04-27 | The Lubrizol Corporation | Concentrates, lubricant compositions and methods for improving fuel economy of internal combustion engine |
DE2842563A1 (de) * | 1978-09-27 | 1980-04-10 | Mannesmann Ag | Verfahren zur erzielung extrem niedriger phosphorgehalte |
US4264458A (en) * | 1979-04-02 | 1981-04-28 | Exxon Research & Engineering Co. | Metalworking lubricant composition |
US4334921A (en) * | 1979-04-16 | 1982-06-15 | Nippon Steel Corporation | Converter steelmaking process |
US4505830A (en) * | 1981-09-21 | 1985-03-19 | The Lubrizol Corporation | Metal working using lubricants containing basic alkali metal salts |
US4416788A (en) * | 1981-10-13 | 1983-11-22 | Atlantic Richfield Company | Metal cutting oil and method for using same |
JPS58207314A (ja) * | 1982-05-28 | 1983-12-02 | Sumitomo Metal Ind Ltd | 鋼の精錬方法 |
DE3245098C2 (de) * | 1982-12-07 | 1990-06-21 | Klöckner-Werke AG, 4100 Duisburg | Zweistufiges Verfahren zum Herstellen von hochwertigen Stählen mit extrem niedrigen P- und S-Gehalten, die im Konverter vorgeschmolzen werden |
US4488903A (en) * | 1984-03-14 | 1984-12-18 | Union Carbide Corporation | Rapid decarburization steelmaking process |
-
1984
- 1984-09-22 DE DE3434894A patent/DE3434894C2/de not_active Expired
-
1985
- 1985-08-21 EP EP85110495A patent/EP0175924B1/de not_active Expired
- 1985-08-21 AT AT85110495T patent/ATE39497T1/de active
- 1985-08-21 DE DE8585110495T patent/DE3567031D1/de not_active Expired
- 1985-08-22 AU AU46540/85A patent/AU569412B2/en not_active Ceased
- 1985-08-28 ZA ZA856561A patent/ZA856561B/xx unknown
- 1985-08-28 FI FI853294A patent/FI77694C/fi not_active IP Right Cessation
- 1985-09-04 ES ES546700A patent/ES8703936A1/es not_active Expired
- 1985-09-05 MX MX8889A patent/MX164702B/es unknown
- 1985-09-11 US US06/774,632 patent/US4604138A/en not_active Expired - Fee Related
- 1985-09-12 CN CN85106853.7A patent/CN1005276B/zh not_active Expired
- 1985-09-13 JP JP60201953A patent/JPS6179709A/ja active Granted
- 1985-09-16 IN IN655/CAL/85A patent/IN163954B/en unknown
- 1985-09-20 BR BR8504605A patent/BR8504605A/pt not_active IP Right Cessation
- 1985-09-20 CA CA000491216A patent/CA1234989A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN100351399C (zh) * | 2001-02-07 | 2007-11-28 | 新日本制铁株式会社 | 生铁熔体脱磷的方法 |
Also Published As
Publication number | Publication date |
---|---|
CN85106853A (zh) | 1987-03-11 |
FI853294A0 (fi) | 1985-08-28 |
AU569412B2 (en) | 1988-01-28 |
ES8703936A1 (es) | 1987-03-16 |
FI77694C (fi) | 1989-04-10 |
FI77694B (fi) | 1988-12-30 |
ATE39497T1 (de) | 1989-01-15 |
EP0175924A1 (de) | 1986-04-02 |
ES546700A0 (es) | 1987-03-16 |
US4604138A (en) | 1986-08-05 |
EP0175924B1 (de) | 1988-12-28 |
JPS6179709A (ja) | 1986-04-23 |
IN163954B (zh) | 1988-12-17 |
AU4654085A (en) | 1986-03-27 |
BR8504605A (pt) | 1986-07-15 |
CA1234989A (en) | 1988-04-12 |
JPH0136525B2 (zh) | 1989-08-01 |
DE3434894C2 (de) | 1986-09-18 |
ZA856561B (en) | 1986-04-30 |
FI853294L (fi) | 1986-03-23 |
DE3567031D1 (en) | 1989-02-02 |
MX164702B (es) | 1992-09-18 |
DE3434894A1 (de) | 1986-04-17 |
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