JPS5852004B2 - Low-hydrogen steel melting process in pure oxygen bottom-blown converter - Google Patents
Low-hydrogen steel melting process in pure oxygen bottom-blown converterInfo
- Publication number
- JPS5852004B2 JPS5852004B2 JP81378A JP81378A JPS5852004B2 JP S5852004 B2 JPS5852004 B2 JP S5852004B2 JP 81378 A JP81378 A JP 81378A JP 81378 A JP81378 A JP 81378A JP S5852004 B2 JPS5852004 B2 JP S5852004B2
- Authority
- JP
- Japan
- Prior art keywords
- blowing
- converter
- steel
- cht
- pure oxygen
- 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.)
- Expired
Links
- 229910000831 Steel Inorganic materials 0.000 title claims description 35
- 239000010959 steel Substances 0.000 title claims description 35
- 239000001257 hydrogen Substances 0.000 title claims description 28
- 229910052739 hydrogen Inorganic materials 0.000 title claims description 28
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 title claims description 14
- 238000010309 melting process Methods 0.000 title claims 2
- 238000007664 blowing Methods 0.000 claims description 38
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 25
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 20
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 12
- 239000001301 oxygen Substances 0.000 claims description 12
- 229910052760 oxygen Inorganic materials 0.000 claims description 12
- 229910052742 iron Inorganic materials 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 8
- 235000019738 Limestone Nutrition 0.000 claims description 6
- 230000004907 flux Effects 0.000 claims description 6
- 239000006028 limestone Substances 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- 238000002844 melting Methods 0.000 claims 1
- 230000008018 melting Effects 0.000 claims 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 20
- 238000002347 injection Methods 0.000 description 13
- 239000007924 injection Substances 0.000 description 13
- 239000007789 gas Substances 0.000 description 11
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 10
- 235000012255 calcium oxide Nutrition 0.000 description 10
- 239000000292 calcium oxide Substances 0.000 description 10
- 238000006356 dehydrogenation reaction Methods 0.000 description 8
- 239000001294 propane Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 150000002431 hydrogen Chemical class 0.000 description 3
- 238000005096 rolling process Methods 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 2
- 238000005261 decarburization Methods 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000011835 investigation Methods 0.000 description 2
- 101100098216 Caenorhabditis elegans rars-1 gene Proteins 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 229910000655 Killed steel Inorganic materials 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 238000010583 slow cooling Methods 0.000 description 1
- 239000002436 steel type Substances 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Description
【発明の詳細な説明】
この発明は、純酸素底吹き転炉の吹錬法の改良、なかで
もとくに、該転炉における低水素鋼の溶製法に関するも
のである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an improvement in the blowing method of a pure oxygen bottom-blown converter, and particularly to a method for producing low hydrogen steel in the converter.
純酸素底吹き転炉は、本質的に水素濃度が高く、これは
、純酸素吹込み用の羽目保護のため、該羽口のまわりに
供給されるプロパンガスのような炭化水素の鋼浴中にお
ける分解によって水素ガスが発生することによると考え
られていた。Pure oxygen bottom-blown converters inherently have a high concentration of hydrogen, which is caused by a steel bath of hydrocarbons such as propane gas being fed around the tuyere to protect the tuyere for pure oxygen blowing. It was thought that this was due to the generation of hydrogen gas by decomposition in
実際に、通常の吹錬方法で操業したときに、転炉の吹止
め時における鋼中水素濃度は、はぼ5〜6Wmlこもの
ぼり、LD転炉鋼の1.5〜3.0pIlfflと比べ
てはるかに高く、平炉鋼とおよそ同レベルである。In fact, when operating in the normal blowing method, the hydrogen concentration in the steel at the time of the converter's blow-off is approximately 5 to 6 Wml, compared to 1.5 to 3.0 pIlffl for LD converter steel. It is much higher and about the same level as open hearth steel.
その結果、たとえば厚板向けの構造用キルド鋼などでは
、圧延工程で徐冷を行うことによって水素を逃がすとか
、あるいは吹錬吹止め温度を高くして、その吹止め後に
あらためてArガスの如きを用いる脱水素処理を行う必
要があり、その倒れもが生産性ならびにコスト上の不利
を伴った。As a result, for example, in structural killed steel for thick plates, it is necessary to slowly cool the hydrogen during the rolling process to release the hydrogen, or to increase the blowing stop temperature and then re-injecting Ar gas such as Ar gas after the blow stop. It was necessary to carry out dehydrogenation treatment, which resulted in disadvantages in terms of productivity and cost.
発明者らは、純酸素底吹き転炉の操業経験を経て、この
場合の吸収水素濃度がプロパンガス吹込み量から予測さ
れる程度をこえて上記のように高い事実につき種々な検
討を重ねた結果、その原因が、とくに吹錬の全期間中鋼
浴内へ継続して添加される含水フラックスたとえば焼石
灰、脱隣フランクスは通常3〜4%の水分を含み、その
分解によって生じる水素の吸収が、上記プロパンガスの
吹込みに由来した水素吸収に加わることを究明した。After gaining experience in operating a pure oxygen bottom-blown converter, the inventors conducted various studies regarding the fact that the absorbed hydrogen concentration in this case is higher than expected from the amount of propane gas blown into the reactor. As a result, the cause of this problem is particularly the absorption of hydrogen produced by the decomposition of water-containing fluxes, such as burnt lime and dephosphorized fluxes, which are continuously added to the steel bath during the whole blowing period, and which usually contain 3 to 4% water. It has been determined that this is added to the hydrogen absorption resulting from the propane gas injection.
そこで、この点の対策であるが、吹錬過程において、脱
炭最減期には鋼浴中に発生する多量のCO+CO2ガス
による希釈のため、事実上の影響がないのに反し、脱炭
効率が低下するに至った吹錬時間、とくに転炉の吹止め
に至る間に溶鋼単位重量当り送酸量でほぼ5 N m/
chtを残す時点以降の期間中は、鋼浴中でCo+C
o2ガス発生量が極端に少くなるため、溶鋼中を浮上す
るバブル中の水素ガス濃度が相対的に高まることとなり
、その結果シーベルトの法則に従い、溶鋼中水素濃度が
上昇し、事実、吹錬中の連続サンプリングによる調査結
果から、第1図のごとき吸収水素濃度と送酸量(吹錬経
過時間)との関係が捕捉されたので、かような実験、調
査結果に基いてこの発明は、転炉の吹止めに至る間に溶
鋼単位重量当り送酸量で少くとも5 N m/ cht
を残しているまでの間に、上記の焼石灰のごとき含水フ
ラックスの吹込みを終了させ、以降はかような含水フラ
ックスを吹込まない吹錬操業を行うことにより、水素濃
度の上昇を防止し、かくして低水素鋼の生産性低下やコ
ストに影響がない、底吹き転炉溶製を可能ならしめたも
のである。Therefore, as a countermeasure for this point, in the blowing process, during the lowest decarburization period, there is a large amount of dilution with CO + CO2 gas generated in the steel bath, so there is virtually no effect, but the decarburization efficiency is The blowing time during which the temperature decreased, especially during the time when the converter stopped blowing, the amount of oxygen supplied per unit weight of molten steel was approximately 5 N m/
During the period after leaving the cht, Co + C in a steel bath.
Since the amount of o2 gas generated becomes extremely small, the hydrogen gas concentration in the bubbles floating in the molten steel becomes relatively high.As a result, according to Sievert's law, the hydrogen concentration in the molten steel increases, and in fact, blowing From the results of the investigation using continuous sampling, the relationship between the absorbed hydrogen concentration and the amount of oxygen supplied (elapsed blowing time) as shown in Figure 1 was determined.Based on the results of such experiments and investigations, this invention The amount of oxygen supplied per unit weight of molten steel is at least 5 N m/cht until the converter stops blowing up.
In order to prevent the hydrogen concentration from increasing, the injection of the above-mentioned hydrated flux such as burnt lime is completed, and subsequent blowing operations are performed without injecting such hydrated flux. Thus, it has become possible to melt low-hydrogen steel in a bottom-blown converter without reducing productivity or affecting costs.
さらに進んでこの発明では、上記した水素ガス濃度の上
昇抑制のみに止まらず、積極的な脱水素を、より有効に
促進する手段として、とくに上記の含水フラックスの吹
込を終了した以降に、鉄鉱石もしくはスケールおよび/
または石灰石の投入または吹込みを行うことの有用性を
、あまた実験の結果究明し、これによって一層水素吸収
の少い低水素鋼の、純酸素底吹転炉による溶製を、生産
性の阻害やコスト増加なしに実現したものである。Further, in this invention, in addition to suppressing the rise in the hydrogen gas concentration described above, as a means to more effectively promote active dehydrogenation, the present invention has been developed to or scale and/or
The effectiveness of adding or blowing limestone was investigated through numerous experiments, and as a result of this, it was found that low hydrogen steel, which absorbs even less hydrogen, could be melted in a pure oxygen bottom-blowing converter without hindering productivity. This was achieved without any increase in costs.
ここに純酸素底吹き転炉で、例えば送酸速度が70ON
rrt1分、プロパン吹込み速度が28N77+3/分
のときには
のH2濃度であるのに対し、たとえば水分4%の焼石灰
を1トン/分吹込んだとすると、H2濃度は、に増加し
、H2濃度の上昇は40%に及ぶ。Here, in a pure oxygen bottom-blown converter, for example, the oxygen feeding rate is 70ON.
The H2 concentration is when rrt1 minute and the propane blowing rate is 28N77+3/minute, but if, for example, burnt lime with a moisture content of 4% is injected at 1 ton/minute, the H2 concentration increases to is up to 40%.
この焼石灰の吹込みを、転炉の吹止め直前である2 N
rrt/ cht (送酸残量)に至るまで継続させた
場合と、転炉吹錬の前半期すなわち2ON7713/c
ht (送酸残量)までに終了させた場合とについて、
吹止め溶鋼の水素含有量の区分毎のヒストグラムを、第
2図a、bに示した。The injection of burnt lime was carried out at 2 N immediately before the converter stopped blowing.
rrt/cht (oxygen supply remaining amount) and the first half of converter blowing, that is, 2ON7713/c
ht (remaining oxygen supply amount),
Histograms of the hydrogen content of blow-stopped molten steel for each category are shown in Figures 2a and 2b.
この発明(第1発明)に従う後者の例で吹止め水素含有
量は、平均4.4pI)Iとなるのに対し、前者の平均
は5.15であって、この発明による効果が明白である
。In the latter example according to this invention (first invention), the blowstop hydrogen content is on average 4.4 pI), whereas in the former case the average is 5.15, and the effect of this invention is obvious. .
次に上述脱水素強制手段としCの鉄鉱石の投入は、
の反応により、またスケールの投入は、
FeO+ C−) Fe + CO↑
2 FeO+ C→2 Fe + CO2↑の反応によ
り、さらには石灰石の投入又は吹込みによっては
の反応を生じてこれらのCOまたはCO2ガスの発生が
プロパンの分解による水素ガスを希釈し鋼浴からの放出
を促進する。Next, as the dehydrogenation forcing means described above, iron ore C is introduced by the reaction, and scale is introduced by the reaction FeO+ C-) Fe + CO↑ 2 FeO+ C→2 Fe + CO2↑, and further limestone The injection or blowing of these gases causes a reaction and the generation of these CO or CO2 gases dilutes the hydrogen gas from the decomposition of propane and promotes its release from the steel bath.
純酸素底吹き吹錬につき上述したと同じ条件でたとえば
鉄鉱石を1トン/分で投入すると、水素濃度は
となり、焼石灰の吹込みをしないときについてさきに計
算した7、4%と比べてさえも水素濃度の低下は22%
にも及び、その効果は明白である。For pure oxygen bottom blowing, if iron ore is injected at 1 ton/min under the same conditions as described above, the hydrogen concentration will be 7.4%, which was calculated earlier when no burnt lime is injected. Even the hydrogen concentration decreased by 22%.
The effect is obvious.
これらの脱水素強制剤の吹錬末期における添加効果の一
例を第3図に示したように、吹止め溶鋼の水素含有量の
有効な低下をもたらし、とくに鉄鉄石、スケールおよび
石灰石の倒れについても4、0 kg/ cht以上8
.0 kg/ chtに至る間に著しいことがわかる。An example of the effect of adding these dehydrogenation forcing agents at the final stage of blowing is shown in Figure 3, which effectively reduces the hydrogen content of blow-stopping molten steel, and particularly reduces the collapse of ferrite, scale, and limestone. 4, 0 kg/cht or more8
.. It can be seen that there is a significant difference in the time it takes to reach 0 kg/cht.
次にこの発明(第2発明)の実施例をのべる。Next, an example of this invention (second invention) will be described.
操業例 1
装入浴鋼量:250.7トン
吹錬時間:i5.1分送酸量 11048ON”焼石灰
吹込:
鉄鉱石投入:
吹止H:
操業例 2
装入溶鋼量:
吹錬時間:
焼石灰吹込:
(41,8NR/cht )
7.2トン(28,7kicht )を吹止19、8
Nrr?/cht前までに吹込8.3トン(33,1k
g/cht )を吹止10、2 Nm/cht前までに
投入
3.7ppm
250.81−ン
15.3分 送酸量 1056ON?71”(42,I
Nrrl/cht )
9.1トンをすべて20.9 Nrt?/chtまで(
吹止め21.2Nm’/cht前)に吹込み
鉄鉱石投入:総量5,0トン(19,9kicht )
のうち、3.Oトノ(12,0kicht )は吹止め
17.7N袷’cht前までに投入、
2.0トン(7,9ky/cht )は吹止め3.8
Nrrl/ch を前〜0.6Nm’/cht前の間に
投入
吹止H:3.Opym
操業例 3
装入溶鋼量:239.6トン
吹錬時間:15.0分送酸量 1041040ON 3
.4NrrVCht )
焼石灰吹込:80トンすべて吹止め19.6Nm’/c
htまでに吹込み
鉄鉱石投入:4.41−ン(18,4kg/cht )
のうち、30、トン(12,5kg/cht )は吹止
め14.5 Nrrl/chtまでに投入、
1.4トン(5,81y/ch t )は吹止め3.6
NrrVcht前に投入
吹止H:2.4ppm
操業例 4
装入溶鋼量:253.Ohン
吹錬時間:15.8分 送酸量 1121ONm’(4
4,3Nホcht )
焼石灰吹込:9.81−ン(38,7kg/cht )
を吹止め20.2 Nrn’1cht前までに吹込み鉄
鉱石投入:3.01−ン(11,9kycht )を吹
止め15、9 Nm3/ ch を前までに投入石灰石
吹込:1.6トン(6,3kg/cht )を吹止め1
、5Nrrtlcht前〜吹止までの間に吹込み吹止H
:2.5p戸
操業例 5
装入溶鋼量:251.31−ン
吹錬時間:15.6分送酸量 11053ON”(41
,9Nm’/cht )
焼石灰吹込:8.6トン(34,2輸にht)を吹止め
18.3 Nm1cht前までに吹込
鉄鉱石投入:4.2トノ(t 6.7kg/cht )
を吹止め13.3 N?rVcht前までに投入
スケール投入:1.51−ン(6,0kg/cht )
を吹止め1.5 Nrt?lch を前に投入
吹止H:2.9pI)m
はじめにのべたように純酸素底吹き転炉で得られる溶製
鋼すなわちQ−BOP鋼は、水素濃度がかなり高く、こ
のため一般に低水素であることが要求される鋼種にあっ
ては、その吹止め濃度を高目にして吹止め、かつ引続い
て高価なArガスをあらためて吹込むことによるような
附加的な脱水素処理を行ったり、あるいは圧延工程にお
いてとくに徐冷を行って水素を逃すことが必要であり、
これらは何れもコストの上昇ならびに生産性の低下を招
き、望ましくなかったのに反して、この発明では上記の
ようにして特別な副原料ないしはガスの類を使用するこ
となく、また余分な処理を要せずに、そして圧延工程に
おける何らの生産性阻害を伴うことなく、LD転炉並み
に水素濃度が充分に低い鋼の、純酸素底吹き転炉による
溶製を可能ならしめ得る。Operation example 1 Amount of charging bath steel: 250.7 tons Blowing time: i5.1 min Oxidation amount 11048 ON” Burnt lime injection: Iron ore input: Blow-off H: Operation example 2 Amount of charged molten steel: Blowing time: Sintering Lime injection: (41,8NR/cht) Blow 7.2 tons (28,7kicht) 19,8
Nrr? /cht before blowing 8.3 tons (33,1k
g/cht) was added before the blow-off 10.2 Nm/cht 3.7 ppm 250.81-15.3 minutes Oxygen supply amount 1056 ON? 71” (42, I
Nrrl/cht) 9.1 tons all 20.9 Nrt? /cht (
Injecting iron ore into the blow stop (21.2 Nm'/cht): total amount 5.0 tons (19.9 kicht)
Of these, 3. The O tonneau (12,0 kicht) was put in before the blowstop was 17.7N, and the 2.0 ton (7,9ky/cht) was put in before the blowstop was 3.8N.
Nrrl/ch before - 0.6 Nm'/ch before blow-off H: 3. Opym operation example 3 Charged molten steel amount: 239.6 tons Blowing time: 15.0 minutes Oxygen feeding amount 1041040ON 3
.. 4NrrVCht) Burnt lime injection: 80 tons all stopped 19.6Nm'/c
Injection of iron ore by ht: 4.41-n (18.4 kg/cht)
Of these, 30 tons (12.5 kg/cht) were put in at the blow stop of 14.5 Nrrl/ch, and 1.4 tons (5,81 y/ch t) were put in at the blow stop of 3.6 Nrrl/ch.
Blow-off H before NrrVcht: 2.4 ppm Operation example 4 Amount of molten steel charged: 253. Ohn blowing time: 15.8 minutes Oxygen supply amount 1121ONm' (4
4,3N hot) Burnt lime injection: 9.81-ton (38,7kg/cht)
Iron ore injection: 3.01-tons (11.9 kycht) was injected before the blow stop of 20.2 Nrn'1ch. Limestone injection: 1.6 tons ( 6.3kg/cht)
, Blow stop H between before 5Nrrtlcht and stop stop.
: 2.5p door operation example 5 Charged molten steel amount: 251.31-ton blowing time: 15.6 minutes Oxygen feeding amount 11053ON" (41
, 9Nm'/cht ) Burnt lime injection: 8.6 tons (34.2 tons/ht) was injected until 18.3 Nm/cht before the blow-off. Iron ore injection: 4.2 tons (t 6.7 kg/cht )
13.3 N? Input scale before rVcht: 1.51-ton (6.0kg/cht)
1.5 Nrt? Blow-off H: 2.9 pI) m As mentioned in the introduction, molten steel obtained in a pure oxygen bottom-blown converter, that is, Q-BOP steel, has a considerably high hydrogen concentration, and therefore is generally low in hydrogen. For steel types that require high dehydrogenation, the dehydrogenation treatment may be performed by increasing the concentration of dehydrogenation, followed by additional dehydrogenation treatment such as by injecting expensive Ar gas again, or During the rolling process, it is necessary to perform slow cooling to release hydrogen.
Both of these methods lead to an increase in cost and a decrease in productivity, which is undesirable.However, in the present invention, as described above, no special auxiliary raw materials or gases are used, and no extra processing is required. It is possible to melt steel in a pure oxygen bottom-blown converter, which has a hydrogen concentration as low as that in an LD converter, without any need for it and without any productivity impediment in the rolling process.
第1図は吹錬途次における溶鋼H濃度の変化のありさま
を示す線図、第2図a、bは焼石灰投入の時期的制限が
もたらす吹止めH分布をあられした比較図表、第3図は
鉄鉱石、スケールおよび石灰石の吹錬末期における投入
又は吹込み量と吹止めHとの関係を示すグラフである。Figure 1 is a diagram showing how the molten steel H concentration changes during the blowing process, Figures 2 a and b are comparison charts showing the blow-stop H distribution caused by the timing restrictions on the addition of burnt lime, and Figure 3 The figure is a graph showing the relationship between the blowstop H and the amount of iron ore, scale, and limestone added or blown at the final stage of blowing.
Claims (1)
錬中の鋼浴内へ添加される含水性フラックス成分の吹込
みを、該転炉の吹止めに至る間に溶鋼単位重量当りの送
酸量で少くとも5Nm’/chtが残されているまでの
間に終了させることを特徴とする純酸素底吹き転炉にお
ける低水素鋼溶製法。 2 純酸素底吹き転炉による低水素鋼の吹錬に際し、吹
錬中の鋼浴内へ添加される含水フラックス取分の吹込み
を、該転炉の吹止めに至る間に溶鋼単位重量当り送酸量
で少くとも5Nm″/chtが残されているまでの間に
終了させ、この終了以降に、鉄鉱石、スケールおよび石
灰石のうら一種又は二種以上を、41q/ cht以上
投入または吹込みすることを特徴とする純酸素底吹き転
炉における低水素鋼溶製法。[Claims] 1. When blowing low-hydrogen steel in a pure oxygen bottom-blowing converter, blowing a hydrous flux component added into the steel bath during blowing until the converter stops blowing. A low hydrogen steel melting process in a pure oxygen bottom-blowing converter, characterized in that the process is terminated until at least 5 Nm'/cht remains in the oxygen flow rate per unit weight of molten steel. 2. When blowing low-hydrogen steel in a pure oxygen bottom-blowing converter, the amount of water-containing flux added to the steel bath during blowing is blown per unit weight of molten steel until the converter stops blowing. The process should be completed until at least 5 Nm''/cht remains in terms of oxygen supply, and after this end, one or more types of iron ore, scale, and limestone should be added or blown in at least 41q/cht. A low hydrogen steel melting method in a pure oxygen bottom-blown converter, which is characterized by:
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP81378A JPS5852004B2 (en) | 1978-01-10 | 1978-01-10 | Low-hydrogen steel melting process in pure oxygen bottom-blown converter |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP81378A JPS5852004B2 (en) | 1978-01-10 | 1978-01-10 | Low-hydrogen steel melting process in pure oxygen bottom-blown converter |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5494419A JPS5494419A (en) | 1979-07-26 |
| JPS5852004B2 true JPS5852004B2 (en) | 1983-11-19 |
Family
ID=11484111
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP81378A Expired JPS5852004B2 (en) | 1978-01-10 | 1978-01-10 | Low-hydrogen steel melting process in pure oxygen bottom-blown converter |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5852004B2 (en) |
-
1978
- 1978-01-10 JP JP81378A patent/JPS5852004B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5494419A (en) | 1979-07-26 |
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