JP2001347351A - Mold powder and continuous casting method - Google Patents

Mold powder and continuous casting method

Info

Publication number
JP2001347351A
JP2001347351A JP2000171155A JP2000171155A JP2001347351A JP 2001347351 A JP2001347351 A JP 2001347351A JP 2000171155 A JP2000171155 A JP 2000171155A JP 2000171155 A JP2000171155 A JP 2000171155A JP 2001347351 A JP2001347351 A JP 2001347351A
Authority
JP
Japan
Prior art keywords
mold powder
mass
mold
content
tio
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
Application number
JP2000171155A
Other languages
Japanese (ja)
Other versions
JP3610885B2 (en
Inventor
Masafumi Hanao
方史 花尾
Yuichi Tsukaguchi
友一 塚口
Masayuki Kawamoto
正幸 川本
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.)
Nippon Steel Corp
Original Assignee
Sumitomo Metal Industries 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 Sumitomo Metal Industries Ltd filed Critical Sumitomo Metal Industries Ltd
Priority to JP2000171155A priority Critical patent/JP3610885B2/en
Publication of JP2001347351A publication Critical patent/JP2001347351A/en
Application granted granted Critical
Publication of JP3610885B2 publication Critical patent/JP3610885B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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

  • Continuous Casting (AREA)

Abstract

PROBLEM TO BE SOLVED: To provide a mold powder and a continuous casting method with which a cast slab having good cleanliness on the surface layer part thereof without generating the longitudinal crack can be obtained. SOLUTION: In the mold powder containing CaO, Si02, Al2O3 and fluorine compound as the basis components, the ratio in mass% of CaO/SiO2 is 1.1-1.5, and 5-15 mass% Al2O3, <=5 mass% of the total of content converted into the oxide of alkaline metals, <=1 mass% ZrO2, 0-8 mass% TiO2 and 4-12 mass% F, are contained, and the viscosity at 1300 deg.C is 2-6 Poise and the solidified point is >=1100 deg.C.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、鋳型内の溶鋼表面
に添加されるモールドパウダに関し、さらにこのモール
ドパウダを用いる連続鋳造方法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a mold powder added to the surface of molten steel in a mold, and further relates to a continuous casting method using the mold powder.

【0002】[0002]

【従来の技術】鋼の連続鋳造では、鋳型内の溶鋼表面に
モールドパウダを添加して鋳造する。通常、モールドパ
ウダには、複数種類の酸化物、フッ素化合物、炭素など
の粉体を混合したものが用いられる。
2. Description of the Related Art In continuous casting of steel, mold powder is added to the surface of molten steel in a mold for casting. Usually, a mixture of powders of a plurality of types of oxides, fluorine compounds, carbon, and the like is used for the mold powder.

【0003】鋳型内の溶鋼表面に添加されたモールドパ
ウダでは、溶鋼からの受熱により、溶鋼表面との接触部
において溶融層が形成される。この溶融層は、鋳型内壁
と凝固殻との間隙に流入し、フィルムを形成する。この
フィルムは、鋳型により冷却された固相部分と、液相部
分との二相からなる。
In a mold powder added to the surface of molten steel in a mold, a molten layer is formed at a contact portion with the surface of the molten steel due to heat received from the molten steel. This molten layer flows into the gap between the inner wall of the mold and the solidified shell, and forms a film. This film is composed of two phases, a solid phase portion cooled by a mold and a liquid phase portion.

【0004】モールドパウダは、溶融層およびフィルム
となった状態において、以下に挙げる役割を担う。 溶鋼の保温および酸化防止 溶鋼中気泡または介在物の吸収 鋳型内壁と凝固殻との潤滑性の確保 凝固殻の冷却速度の調整 連続鋳造による鋳片の表面品質に及ぼすモールドパウダ
の影響は大きく、鋳片表面に発生するディプレッショ
ン、または縦割れに対しては、上記役割の中でも、の
凝固殻の冷却速度の調整が重要である。鋳型内の凝固殻
の冷却速度を均一化することにより、凝固殻の厚さは幅
方向に均一になり、凝固収縮により生じる応力が緩和さ
れ、表面に発生するディプレッションまたは縦割れの発
生を抑制できる。
[0004] The mold powder plays the following roles in the state of a molten layer and a film. Heat retention and prevention of oxidation of molten steel Absorption of bubbles or inclusions in molten steel Ensuring lubricity between inner wall of mold and solidified shell Adjusting cooling rate of solidified shell The effect of mold powder on the surface quality of slab by continuous casting is large, Adjustment of the cooling rate of the solidified shell is important for depletion or vertical cracks generated on one surface, among the above roles. By uniformizing the cooling rate of the solidified shell in the mold, the thickness of the solidified shell becomes uniform in the width direction, the stress caused by solidification shrinkage is relaxed, and the occurrence of depletion or vertical cracks generated on the surface can be suppressed .

【0005】モールドパウダのフィルム中に、その冷却
過程で結晶が析出すると、フィルムの伝熱抵抗が大きく
なることから、鋳片の凝固収縮が抑制され鋳型壁への密
着性が増し、鋳型内の凝固殻の不均一冷却が防止できる
ことから、従来より、フィルム中に結晶析出を促進する
方法が提案されてきた。
When crystals are precipitated in the mold powder film during the cooling process, the heat transfer resistance of the film increases, so that the solidification shrinkage of the slab is suppressed, the adhesion to the mold wall is increased, and the inside of the mold is reduced. Conventionally, a method for promoting crystal precipitation in a film has been proposed because uneven cooling of a solidified shell can be prevented.

【0006】たとえば 特開平5−15955号公報に
は、モールドパウダ中に含有されるCaOと、CaF2
として存在すると推定されるCa分をCaOに換算した
ものとの和として、下記(C)式で定義されるT.Ca
OのSiO2 に対する質量%の比T.CaO/SiO2
を0.9〜1.3程度に大きくし、フィルム中に結晶を
析出させて、鋳型内の凝固殻の冷却速度を均一にし、か
つ緩冷却することが提案されている。
For example, JP-A-5-15955 discloses that CaO contained in mold powder and CaF 2
As the sum of the Ca component estimated to be present as CaO converted to CaO, the T.C. Ca
% Of O to SiO 2 CaO / SiO 2
Is increased to about 0.9 to 1.3, crystals are precipitated in the film, the cooling rate of the solidified shell in the mold is made uniform, and the cooling is performed slowly.

【0007】しかし、単にモールドパウダの塩基度(C
aO/SiO2 、またはT.CaO/SiO2 )を高め
て、フィルム中に結晶を多く析出させる方法では、結晶
が析出した部分のフィルムの体積が収縮し、鋳型と凝固
殻との間に空隙が生じやすくなる。鋳型と凝固殻との間
に空隙が生じると、伝熱抵抗が飛躍的に増大し、凝固殻
に局部的な凝固遅れを生じる場合がある。凝固遅れが生
じた凝固殻の部分では、縦割れなどが発生しやすい。
However, the basicity of the mold powder (C
aO / SiO 2 or T.A. In the method of increasing CaO / SiO 2 ) to precipitate a large amount of crystals in the film, the volume of the film where the crystals are deposited shrinks, and voids are easily formed between the mold and the solidified shell. When a gap is formed between the mold and the solidified shell, heat transfer resistance is dramatically increased, and a local solidification delay may occur in the solidified shell. Longitudinal cracks and the like are likely to occur in the portion of the solidified shell where solidification delay has occurred.

【0008】そこで、特開平7−214263号公報に
は、モールドパウダの塩基度を0.6〜0.9とし、結
晶析出の促進剤であるZrO2 、TiO2 、CeO2
合計の含有率を1質量%以下とし、かつ凝固点を115
0℃以上とすることにより、モールドパウダのフィルム
中の結晶析出量が過度になることなく、適正に保つ方法
が提案されている。これにより、鋳型内の凝固殻の冷却
速度の均一化が促進され、表面に発生するディプレッシ
ョンまたは縦割れの発生が抑制されるのが期待できる。
Therefore, Japanese Patent Application Laid-Open No. Hei 7-214263 discloses that the basic content of mold powder is set to 0.6 to 0.9, and the total content of ZrO 2 , TiO 2 and CeO 2 which are accelerators for crystal precipitation. To 1% by mass or less, and the freezing point is 115
A method has been proposed in which the temperature is kept at 0 ° C. or higher so that the amount of crystals precipitated in the film of the mold powder does not become excessive and is appropriately maintained. Thereby, uniformization of the cooling rate of the solidified shell in the mold is promoted, and it can be expected that generation of depletion or vertical cracks generated on the surface is suppressed.

【0009】しかし、この方法では、鋳型内の溶鋼中に
Al23 、MnO等の酸化物が増加する場合があり、
これらの酸化物が鋳型内の凝固殻に捕捉され、鋳片表層
部の清浄性が悪くなりやすい。これら鋳片を素材として
熱間圧延する製品に表面疵などが発生しやすい。
However, according to this method, oxides such as Al 2 O 3 and MnO may increase in molten steel in a mold,
These oxides are trapped in the solidified shell in the mold, and the cleanliness of the surface layer of the slab tends to deteriorate. Surface flaws and the like are likely to occur in products that are hot rolled using these slabs as raw materials.

【0010】[0010]

【発明が解決しようとする課題】本発明は、鋳片表面の
ディプレッションまたは縦割れの発生を防止でき、さら
に、鋳片表層部の清浄性も良好で、品質の良好な鋳片を
得ることができるモールドパウダ、およびそのモールド
パウダを用いる連続鋳造方法を提供することを目的とす
る。
SUMMARY OF THE INVENTION According to the present invention, it is possible to prevent the occurrence of depletion or vertical cracks on the surface of a slab and to obtain a slab of good quality with good cleanliness of the surface layer of the slab. It is an object of the present invention to provide a mold powder that can be used and a continuous casting method using the mold powder.

【0011】[0011]

【課題を解決するための手段】本発明の要旨は、下記
(1)および(2)に示すモールドパウダ、および下記
(3)に示す連続鋳造方法にある。 (1)CaO、SiO2 、Al23 およびフッ素化合
物を基本成分とするモールドパウダであって、CaOの
SiO2 に対する質量%の比CaO/SiO2 が1.1
〜1.5であり、Al23 を5〜15質量%、アルカ
リ金属を酸化物換算含有率の合計で5質量%以下、Zr
2 を1質量%以下、TiO2 を0〜8質量%、Fを4
〜12質量%含有し、1300℃における粘度が2〜6
poise、凝固点が1100℃以上である連続鋳造用
のモールドパウダ。 (2)Al23 、TiO2 およびFの含有率が、下記
(A)式を満足する上記(1)に記載の連続鋳造用のモ
ールドパウダ。 2≦(Al23 )×(TiO2)≦10+15×(F)・・・(A) ここで、(Al23 ):モールドパウダ中のAl2
3 含有率(質量%) (TiO2):モールドパウダ中のTiO2 含有率(質
量%) (F):モールドパウダ中のF含有率(質量%) (3)上記(1)または(2)に記載のモールドパウダ
を用いる連続鋳造方法であって、下記(B)式で定義さ
れる溶鋼の化学組成Cpとモールドパウダ中のAl2
3 含有率との間の関係が、下記(C)式または(D)式
を満足する条件で鋳造する連続鋳造方法。 Cp=C+0.02×Mn+0.04×Ni−0.01×Si +0.02×Cr+0.07×S・・・(B) ここで、C、Mn、Ni、Si、CrおよびS:溶鋼中
の含有率(質量%) |Cp−0.12|≦0.05の場合; 5+2000×|Cp−0.12|2 ≦(Al23 )≦ 10+2000×|Cp−0.12|2 ・・・(C) |Cp−0.12|>0.05の場合; 10≦(Al23 )≦15 ・・・(D) ここで、|Cp−0.12|:Cpの値から0.12を
引いた値の絶対値 (Al23 ):モールドパウダ中のAl23 含有率
(質量%) 本発明者らは、下記(a)の知見に基づいて、下記
(b)および(c)の対策を採ることにより前述の課題
を解決した。 (a)モールドパウダの塩基度が0.6〜0.9と低い
場合に、鋳型内の溶鋼中にAl23 、MnO等の酸化
物が増加するのは、溶融層中のSiO2 の活量が高くな
り、鋳型内の溶鋼とモールドパウダの溶融層との界面に
おいて、Al、Mn等の溶鋼中成分が酸化されやすくな
るからである。
The gist of the present invention resides in a mold powder shown in the following (1) and (2) and a continuous casting method shown in the following (3). (1) CaO, and SiO 2, Al 2 O 3 and fluorine compound a mold powder having a basic composition, mass% ratio CaO / SiO 2 with respect to SiO 2 of CaO is 1.1
To 1.5, 5 to 15% by mass of Al 2 O 3 , 5% by mass or less in total of alkali metal conversion contents, Zr
O 2 1 wt% or less, the TiO 2 0 to 8 wt%, the F 4
And a viscosity at 1300 ° C of 2 to 6%.
Poise, mold powder for continuous casting having a solidification point of 1100 ° C. or higher. (2) The mold powder for continuous casting according to the above (1), wherein the contents of Al 2 O 3 , TiO 2 and F satisfy the following formula (A). 2 ≦ (Al 2 O 3 ) × (TiO 2 ) ≦ 10 + 15 × (F) (A) where (Al 2 O 3 ): Al 2 O in the mold powder
( 3 ) Content (% by mass) (TiO 2 ): Content of TiO 2 in mold powder (% by mass) (F): Content of F in mold powder (% by mass) (3) The above (1) or (2) Wherein the chemical composition Cp of molten steel defined by the following formula (B) and Al 2 O in the mold powder are provided.
3 the relationship between the content of a continuous casting method for casting under conditions satisfying the following formula (C) or (D) type. Cp = C + 0.02 × Mn + 0.04 × Ni-0.01 × Si + 0.02 × Cr + 0.07 × S (B) Here, C, Mn, Ni, Si, Cr and S: in molten steel Content (% by mass) | Cp−0.12 | ≦ 0.05; 5 + 2000 × | Cp−0.12 | 2 ≦ (Al 2 O 3 ) ≦ 10 + 2000 × | Cp−0.12 | 2.・ (C) When | Cp−0.12 |>0.05; 10 ≦ (Al 2 O 3 ) ≦ 15 (D) where | Cp−0.12 |: 0 from the value of Cp .12 Absolute value of the value obtained by subtracting 12 (Al 2 O 3 ): Al 2 O 3 content in the mold powder (% by mass) Based on the following findings (a), the present inventors have made the following (b) The above-mentioned problem has been solved by taking the measures (a) and (c). (A) When the basicity of the mold powder is as low as 0.6 to 0.9, the increase in oxides such as Al 2 O 3 and MnO in the molten steel in the mold is caused by the SiO 2 in the molten layer. This is because the activity is increased, and components in the molten steel such as Al and Mn are easily oxidized at the interface between the molten steel in the mold and the molten layer of the mold powder.

【0012】そこで、鋳型内の凝固殻の冷却速度を均一
化するには、モールドパウダの塩基度を高めることが重
要である。しかし、モールドパウダの塩基度を高め、フ
ィルム中に結晶を多く析出させる方法では、鋳型と凝固
殻との間に空隙が生じ、凝固殻に局部的な凝固遅れを生
じやすいという課題がある。
Therefore, in order to make the cooling rate of the solidified shell in the mold uniform, it is important to increase the basicity of the mold powder. However, the method of increasing the basicity of the mold powder and causing a large amount of crystals to precipitate in the film has a problem that voids are formed between the mold and the solidified shell, and local solidification delay is likely to occur in the solidified shell.

【0013】本発明者らは、CaO、SiO2 およびフ
ッ素化合物を基本成分とするモールドパウダにおいて、
CaOのSiO2 に対するCaOの質量%の比CaO/
SiO2 が1.1〜1.5であっても、Al23 を5
〜15質量%配合することにより、フィルム中の結晶の
析出が過度になることなく、鋳型内の凝固殻冷却を均一
な状態に維持することが可能であることを見いだした。
両性酸化物であるAl 23 を配合すると、塩基度の高
いモールドパウダの溶融層中では、Al23が酸性的
な存在となり、フィルム中の結晶の析出が適度に抑制さ
れるのである。(b)そこで、本発明のモールドパウダ
では、上記(a)の知見に基づき、CaO、SiO2
Al23 およびフッ素化合物を基本成分とし、前述の
(1)に示す組成を有するモールドパウダとする。
The present inventors have proposed CaO, SiOTwo And
In a mold powder containing a nitrogen compound as a basic component,
CaO SiOTwo Ratio of mass% of CaO to CaO /
SiOTwo Is 1.1 to 1.5, AlTwo OThree 5
By blending % 15% by mass,
Uniform cooling of solidified shell in the mold without excessive precipitation
It has been found that it is possible to maintain the state.
Al, an amphoteric oxide Two OThree When combined with
Al in the molten layer of the mold powderTwo OThreeIs acidic
And the precipitation of crystals in the film is moderately suppressed.
It is done. (B) Therefore, the mold powder of the present invention
Then, based on the knowledge of the above (a), CaO, SiOTwo ,
AlTwo OThree And a fluorine compound as a basic component,
A mold powder having the composition shown in (1) is used.

【0014】これにより、塩基度が1.1〜1.5と高
くても、フィルム中の結晶の析出を適度に抑制し、鋳型
内の凝固殻冷却を均一化できる。さらに、塩基度が高い
ので、鋳型内の溶鋼中にAl23 、MnOなどの酸化
物が増加することを防止できる。 (c)本発明の方法では、前述の(B)式で定義される
溶鋼の化学組成Cpとモールドパウダ中のAl23
有率との間の関係が、前述の(C)式または(D)式を
満足する条件で鋳造する。
Thus, even if the basicity is as high as 1.1 to 1.5, the precipitation of crystals in the film is appropriately suppressed, and the cooling of the solidified shell in the mold can be made uniform. Further, since the basicity is high, it is possible to prevent an increase in oxides such as Al 2 O 3 and MnO in the molten steel in the mold. (C) In the method of the present invention, the relationship between the chemical composition Cp of molten steel defined by the above formula (B) and the Al 2 O 3 content in the mold powder is determined by the above formula (C) or ( D) Cast under conditions that satisfy the formula.

【0015】|Cp−0.12|は、鋼の化学組成が亜
包晶反応を起こしやすい組成かどうかを示す指標であ
る。亜包晶反応を起こす鋼の鋳片表面に縦割れが発生し
やすいことは、よく知られている。そこで、|Cp−
0.12|≦0.05の場合、すなわち、亜包晶反応を
起こしやすい鋼では、モールドパウダ中のAl23
有率を、前述の(C)式を満足するように、低い含有率
とする。
| Cp-0.12 | is an index indicating whether or not the chemical composition of steel is a composition that easily causes a subperitectic reaction. It is well known that vertical cracks are likely to occur on the surface of a steel slab that causes a subperitectic reaction. Therefore, | Cp-
In the case of 0.12 | ≦ 0.05, that is, in a steel which is liable to cause a subperitectic reaction, the Al 2 O 3 content in the mold powder is set to a low content so as to satisfy the above formula (C). And

【0016】Al23 含有率を低くくして、フィルム
中の結晶の析出を適度に増加させ、亜包晶反応に伴う凝
固殻収縮を抑制し鋳型壁への密着性を高めることによ
り、鋳型内の凝固殻不均一冷却を抑制し、鋳片表面の縦
割れの発生を防止するのである。
By lowering the Al 2 O 3 content to moderately increase the precipitation of crystals in the film, suppressing the shrinkage of the solidified shell due to the subperitectic reaction, and increasing the adhesion to the mold wall, It suppresses uneven cooling of the solidified shell inside and prevents the occurrence of vertical cracks on the slab surface.

【0017】[0017]

【発明の実施の形態】本発明のモールドパウダおよびこ
のモールドパウダを用いた連続鋳造方法について、以下
に具体的に説明する。
DESCRIPTION OF THE PREFERRED EMBODIMENTS The mold powder of the present invention and a continuous casting method using the mold powder will be specifically described below.

【0018】本発明のパウダは、CaO、SiO2 、A
23 およびフッ素化合物を基本組成としている。そ
の含有率は、CaOが25〜50%程度、SiO2 が2
0〜40%程度、Al23 が5〜15%、Fが4〜1
2%である。さらに、アルカリ金属を酸化物換算含有率
の合計で5質量%以下、ZrO2 を1質量%以下含有
し、また、必要に応じてTiO2 を0〜8質量%の範囲
で含有することができる。
The powder of the present invention comprises CaO, SiO 2 , A
The basic composition is l 2 O 3 and a fluorine compound. The content is about 25 to 50% for CaO and 2 for SiO2.
About 0 to 40%, Al 2 O 3 5 to 15%, F 4 to 1
2%. Further, the total content of alkali metals in terms of oxide is 5% by mass or less, ZrO 2 is 1% by mass or less, and TiO 2 can be contained in a range of 0 to 8% by mass as necessary. .

【0019】本発明のパウダを製造する際に使用する原
料は、一般的に使用されているもので構わない。CaO
原料として生石灰、石灰石、セメント、SiO2 原料と
しては珪砂、軽藻土、Al23 原料としてはアルミ
ナ、F原料としては蛍石、アルカリ金属の酸化物とし
て、たとえば、Na2 O原料としてはソーダ灰、炭酸ナ
トリウム、フッ化ナトリウム、TiO2 原料としてはル
チルサンド、ZrO2 原料としてはジルコンサンドなど
が挙げられる。また、原料の粒度は100μm以下の粉
末が望ましい。なお、これらの原料にはFe23 、F
34 等の酸化物が含有され、パウダにも不可避的に
含まれるようになるが、これらの不純物が存在しても、
とくに差し支えない。モールドパウダのCaO、SiO
2 の含有率についてはすでに述べたが、これらの含有率
は目安を示すものであり、本発明では、CaO/SiO
2 の値を1.1〜1.5とする。塩基度が1.1未満で
は、溶鋼酸化の抑制効果は小さい。また、塩基度が1.
5を超えると、フィルム中に過度に結晶が析出し、さら
に、凝固点が過剰に高くなるので、鋳型内における潤滑
性の悪化や凝固殻の冷却が不均一になりやすいという弊
害を生じる。
The raw materials used for producing the powder of the present invention may be those generally used. CaO
Raw lime, limestone, cement as raw materials, silica sand and light algae soil as SiO 2 raw materials, alumina as Al 2 O 3 raw materials, fluorite as F raw materials, oxides of alkali metals, for example, Na 2 O raw materials Examples of soda ash, sodium carbonate, sodium fluoride, and TiO 2 raw materials include rutile sand, and ZrO 2 raw materials include zircon sand. Further, it is preferable that the raw material has a particle size of 100 μm or less. These raw materials include Fe 2 O 3 , F
Although oxides such as e 3 O 4 are contained and are inevitably contained in powder, even if these impurities exist,
No problem. CaO, SiO of mold powder
Although the contents of 2 have already been described, these contents are only for reference, and in the present invention, CaO / SiO
The value of 2 is set to 1.1 to 1.5. When the basicity is less than 1.1, the effect of suppressing molten steel oxidation is small. Further, the basicity is 1.
If it exceeds 5, crystals are excessively precipitated in the film, and the solidification point becomes excessively high. Therefore, there is a problem that lubricity in the mold is deteriorated and cooling of the solidified shell tends to be uneven.

【0020】モールドパウダ中のAl23 含有率は5
〜15質量%とする。5質量%未満では、フィルム中に
結晶が過度に析出し、鋳型内の凝固殻の冷却が不均一に
なりやすい。また、15質量%を超えると、モールドパ
ウダの溶融層の粘度が過度に上昇したり、凝固点が高く
なり、溶融層が鋳型と凝固殻の隙間に流れ込みにくくな
る。
The Al 2 O 3 content in the mold powder is 5
To 15% by mass. If it is less than 5% by mass, crystals are excessively precipitated in the film, and the cooling of the solidified shell in the mold tends to be uneven. On the other hand, when the content exceeds 15% by mass, the viscosity of the molten layer of the mold powder is excessively increased, the solidification point is increased, and the molten layer is less likely to flow into the gap between the mold and the solidified shell.

【0021】モールドパウダ中のアルカリ金属の酸化物
換算含有率の合計は5質量%以下とする。アルカリ金属
の酸化物は、通常の原料配合によってモールドパウダ中
に含有される。ただし、5質量%を超えて含有すると、
鋳型内において未溶融のモールドパウダが焼結しやす
く、鋳型内溶鋼保温性の悪化を来す。さらに、溶融層が
鋳型と凝固殻の隙間に均一に流れ込みにくくなる。した
がって、アルカリ金属の酸化物換算含有率の合計を5質
量%以下とする。
The total content of alkali metal oxides in the mold powder in terms of oxide is 5% by mass or less. The oxide of the alkali metal is contained in the mold powder by a usual raw material blending. However, if the content exceeds 5% by mass,
Unmelted mold powder easily sinters in the mold, which deteriorates the heat retention of molten steel in the mold. Further, it becomes difficult for the molten layer to uniformly flow into the gap between the mold and the solidified shell. Therefore, the total content of alkali metal in terms of oxide is set to 5% by mass or less.

【0022】モールドパウダ中のZrO2 の含有率は1
質量%以下とする。ZrO2 は、TiO2 の原料を配合
する場合に、モールドパウダ中に含有される。ただし、
モールドパウダ中に数%程度の少量が存在した状態で
も、結晶の析出が促進され、また凝固点の上昇が著し
い。したがって、ZrO2 の含有率は1質量%以下とす
る。
The content of ZrO 2 in the mold powder is 1
% By mass or less. ZrO 2 is contained in the mold powder when a TiO 2 raw material is blended. However,
Even in a state where a small amount of about several percent is present in the mold powder, the precipitation of crystals is promoted and the freezing point is significantly increased. Therefore, the content of ZrO 2 is set to 1% by mass or less.

【0023】モールドパウダ中のFの含有率は4〜12
質量%とする。Fは、凝固点の調整および適度の結晶析
出を目的として含有させる。4質量%未満では、その効
果が小さい。12質量%を超えると、溶融層の粘度が過
度に低下し、溶鋼中に巻き込まれやすいばかりか、鋳型
と凝固殻との隙間に過度に流れ込み、かえって鋳片表面
に縦割れが発生しやすい。
The F content in the mold powder is 4 to 12
% By mass. F is contained for the purpose of adjusting the freezing point and moderate crystal precipitation. If it is less than 4% by mass, the effect is small. If the content exceeds 12% by mass, the viscosity of the molten layer is excessively reduced, so that the molten layer is not only easily entangled in the molten steel, but also excessively flows into the gap between the mold and the solidified shell, and rather, longitudinal cracks are easily generated on the slab surface.

【0024】モールドパウダ中には、必要に応じてTi
2 を添加する。その際、TiO2の含有率は0〜8質
量%とする。TiO2 は、従来、フィルム中への結晶析
出の促進剤として用いられているが、本発明では、適度
のTiO2 添加により、凝固点の低下に著しい効果があ
り、さらに、凝固点が低下しても、粘度が低下しにくい
ことを見出した。そこで、粘度を下げずに、凝固点を低
下させる目的で、TiO2 を0〜8質量%含有させるこ
とができる。
In the mold powder, if necessary,
The O 2 is added. At that time, the content of TiO 2 is set to 0 to 8% by mass. TiO 2 has been conventionally used as an accelerator for crystal precipitation in a film, but in the present invention, the addition of a suitable amount of TiO 2 has a remarkable effect on lowering the freezing point. It was found that the viscosity was hardly reduced. Therefore, without decreasing the viscosity, for the purpose of lowering the freezing point, the TiO 2 may be contained 0-8 wt%.

【0025】モールドパウダの凝固点は1100℃以上
とし、1300℃における粘度は2〜6poiseとす
る。また、望ましい凝固点の上限は1300℃である。
凝固点を上記範囲とすることにより、フィルム中の結晶
析出サイトである固相部分の厚みを確保することができ
る。また、粘度を上記範囲とすることにより、溶融モー
ルドパウダが鋳型内の溶鋼中に巻き込まれたりすること
を防止できる。
The solidification point of the mold powder is 1100 ° C. or higher, and the viscosity at 1300 ° C. is 2 to 6 poise. The upper limit of the desired freezing point is 1300 ° C.
By setting the solidification point in the above range, the thickness of the solid phase portion, which is a crystal precipitation site in the film, can be ensured. By setting the viscosity in the above range, the molten mold powder can be prevented from being caught in the molten steel in the mold.

【0026】モールドパウダ中のAl23 、TiO2
およびFの含有率は、前述の(A)式を満足する範囲と
するのが望ましい。本発明者らは、TiO2 の望ましい
含有率は、Al23 およびFの含有率により影響を受
けることを見出した。つまり、TiO2 およびAl2
3 の含有率の積を一定範囲内とすることにより、モール
ドパウダの凝固点、または溶融層の粘度を適正に調整す
ることが容易になるのである。さらに、TiO2 および
Al23 の含有率の積の適正な範囲が、F含有率の影
響を受けることも見出した。TiO2 およびAl23
の含有率の積が2未満では、凝固点の低下量が小さく、
前述の(A)式の右辺の値を超えると、凝固点が高くな
りやすい。
Al 2 O 3 , TiO 2 in mold powder
It is desirable that the contents of F and F fall within a range that satisfies the expression (A). The present inventors have found that the desired content of TiO 2 is affected by the content of Al 2 O 3 and F. That is, TiO 2 and Al 2 O
By setting the product of the content of 3 within a certain range, it becomes easy to appropriately adjust the solidification point of the mold powder or the viscosity of the molten layer. Furthermore, it has been found that the appropriate range of the product of the TiO 2 and Al 2 O 3 contents is affected by the F content. TiO 2 and Al 2 O 3
If the product of the content ratios is less than 2, the decrease in the freezing point is small,
If the value exceeds the value on the right side of the above-described formula (A), the freezing point tends to increase.

【0027】本発明の方法では、前述の(B)式で定義
される溶鋼の化学組成Cpとモールドパウダ中のAl2
3 含有率との間の関係が、前述の(C)式または
(D)式を満足する条件で鋳造する。|Cp−0.12
|≦0.05の場合、すなわち、亜包晶反応を起こしや
すい鋼では、モールドパウダ中のAl23 含有率を、
前述の(C)式を満足するように、低い含有率とする。
Al23 含有率を低くくして、フィルム中の結晶の析
出を適度に増加させ、亜包晶反応に伴う凝固殻収縮を抑
制し鋳型壁への密着性を高めることにより、鋳型内の凝
固殻不均一冷却を抑制し、鋳片表面の縦割れの発生を防
止するのである。
In the method of the present invention, the chemical composition Cp of the molten steel defined by the above-mentioned formula (B) and the Al 2 in the mold powder are used.
Casting is performed under the condition that the relationship with the O 3 content satisfies the above-mentioned formula (C) or (D). | Cp-0.12
In the case of | ≦ 0.05, that is, in a steel which is liable to cause a subperitectic reaction, the Al 2 O 3 content in the mold powder is
The content is set low so as to satisfy the above-mentioned formula (C).
By lowering the Al 2 O 3 content to moderately increase the precipitation of crystals in the film, suppressing solidification shell shrinkage associated with the subperitectic reaction and increasing the adhesion to the mold wall, solidification in the mold The uneven cooling of the shell is suppressed, and the occurrence of vertical cracks on the surface of the slab is prevented.

【0028】|Cp−0.12|>0.05の場合に
は、とくに、Al23 含有率を低くしなくても、鋳片
表面の縦割れの発生を防止できる。むしろ、Al23
含有率を10〜15質量%とやや多くすることにより、
モールドパウダの溶融層の粘度を適度に高くする、とと
もにフィルム中の過度な結晶析出を抑制し鋳型内の凝固
殻冷却を均一化するのがよい。
When | Cp-0.12 |> 0.05, the occurrence of vertical cracks on the surface of the slab can be prevented without reducing the Al 2 O 3 content. Rather, Al 2 O 3
By slightly increasing the content to 10 to 15% by mass,
It is desirable to increase the viscosity of the molten layer of the mold powder to an appropriate level, to suppress excessive crystal precipitation in the film, and to uniformly cool the solidified shell in the mold.

【0029】[0029]

【実施例】垂直曲げ型連続鋳造機を用いて、厚さ230
mm、幅1220mmの鋳片に、速度1.1m/分また
は1.4m/分で鋳造した。用いた鋼の化学組成を表1
に示す。鋼は低炭素鋼および亜包晶系の中炭素鋼であ
り、表1には、本発明の方法で定義する化学組成Cpを
示す。低炭素鋼のCpは0.043質量%で、中炭素鋼
のCpは0.117質量%であり、それぞれ|Cp−
0.12|は、低炭素鋼が0.077、中炭素鋼が0.
003であり、また、中炭素鋼の|Cp−0.12|2
は、0.000009となる。したがって、低炭素鋼を
鋳造する場合の望ましいモールドパウダ中のAl23
含有率は、前述の(D)式より10〜15質量%、中炭
素鋼を鋳造する場合の望ましいモールドパウダ中のAl
23 含有率は、前述の(C)式より5〜10質量%と
なる。
EXAMPLE Using a vertical bending type continuous casting machine, a thickness of 230 mm was used.
mm and a width of 1220 mm were cast at a speed of 1.1 m / min or 1.4 m / min. Table 1 shows the chemical composition of the steel used.
Shown in The steel is a low carbon steel and a hypoperitectic medium carbon steel, and Table 1 shows the chemical composition Cp defined by the method of the present invention. Cp of low carbon steel is 0.043% by mass, Cp of medium carbon steel is 0.117% by mass, and | Cp−
0.12 | is 0.077 for low carbon steel and 0.0 for medium carbon steel.
003, and | Cp−0.12 | 2 of medium carbon steel.
Is 0.000009. Therefore, when casting low-carbon steel, Al 2 O 3 in the mold powder is desirable.
The content is 10 to 15% by mass according to the above formula (D). Desirable Al in the mold powder when casting medium carbon steel is used.
The content of 2 O 3 is 5 to 10% by mass from the formula (C) described above.

【0030】[0030]

【表1】 試験に用いたモールドパウダの組成を表2に示す。モー
ルドパウダaは塩基度と粘度、モールドパウダbは塩基
度、モールドパウダcはAl23 含有率、モールドパ
ウダdはAl23 含有率と粘度、モールドパウダeは
TiO2 含有率が、それぞれ発明で規定する条件を外れ
ているモールドパウダである。試験条件および試験結果
を表3に示す。
[Table 1] Table 2 shows the composition of the mold powder used in the test. Mold powder a has basicity and viscosity, mold powder b has basicity, mold powder c has Al 2 O 3 content, mold powder d has Al 2 O 3 content and viscosity, and mold powder e has TiO 2 content. Mold powders that do not satisfy the conditions specified in the invention. Table 3 shows the test conditions and test results.

【0031】[0031]

【表2】 [Table 2]

【表3】 表3中に示す指標の中で、「のろピン」は、鋳片表面を
スカーフィングした際に認められたのろかみ疵およびピ
ンホール疵の発生個数である。指標A:なし、指標B:
1〜5個、指標C:6〜10個、指標D:11〜20
個、指標E:21〜50個、指標F:51個以上を示
し、指標AおよびBは、とくに問題のない発生個数であ
る。また、「縦割れ」は、鋳造した鋳片のうち、縦割れ
の発生した分子の割合である。指標A:3%未満、指標
B:3%以上6%未満、指標C:6%以上10%未満、
指標D:10%以上であり、指標AおよびBは、とくに
問題のない発生状況である。さらに「銅板温度変動」
は、鋳造中における鋳型銅板に埋設した熱電対の温度変
動量であり、指標小:±3℃未満、指標中:±10℃未
満、指標大:±10℃以上であり、指標小および中は、
とくに問題のない状況である。
[Table 3] Among the indices shown in Table 3, "Noro Pin" is the number of occurrences of the lazy flaws and pinhole flaws observed when the slab surface was scarfed. Index A: None, Index B:
1 to 5, index C: 6 to 10, index D: 11 to 20
, Index E: 21 to 50, index F: 51 or more, and the indexes A and B are the number of occurrences without any problem. The “vertical crack” is the ratio of molecules in which a vertical crack has occurred in the cast slab. Index A: less than 3%, Index B: 3% or more and less than 6%, Index C: 6% or more and less than 10%,
Indices D: 10% or more, and indices A and B are occurrence situations without any particular problems. Furthermore, "copper plate temperature fluctuation"
Is the temperature variation of the thermocouple buried in the mold copper plate during casting, small index: less than ± 3 ° C, medium index: less than ± 10 ° C, large index: ± 10 ° C or more. ,
There is no problem in particular.

【0032】低炭素鋼を速度1.4m/分で鋳造した試
験では、比較例の試験No.6と比べて、本発明例の試
験No.1〜No.5では、いずれものろかみ疵および
ピンホール疵が減少し、鋳片表面品質の向上しているこ
とがわかる。比較例の試験No.7およびNo.10で
は、凝固点がいずれも1300℃以上と高く、鋳造に使
用出来なかった。比較例の試験No.8およびNo.9
では、結晶析出が過多あるいは不安定であるため、鋳型
銅板温度の変動が大きく、縦割れが発生するものもあっ
た。また、凝固点または粘度が高いために潤滑性が悪
く、鋳片表面には拘束痕等の不良部が多く見られた。
In the test in which low carbon steel was cast at a speed of 1.4 m / min, the test No. In comparison with Test No. 6, Test No. 1 to No. In the case of No. 5, it can be seen that all of the flaws and pinhole flaws are reduced and the surface quality of the slab is improved. Test No. of the comparative example. 7 and No. 7 In No. 10, the solidification point was as high as 1300 ° C. or more, and it could not be used for casting. Test No. of the comparative example. 8 and No. 9
In this case, since the crystal precipitation was excessive or unstable, the temperature of the mold copper plate greatly fluctuated, and in some cases, vertical cracks occurred. In addition, since the solidification point or the viscosity was high, the lubricity was poor, and many defective portions such as restraint marks were observed on the slab surface.

【0033】中炭素鋼を速度1.1m/分で鋳造した試
験では、比較例の試験No.16と比べて、本発明例の
試験No.11〜No.15では、いずれものろかみ疵
およびピンホール疵、縦割れ、および鋳型銅板温度の変
動がいずれも減少し、鋳片表面品質の向上していること
がわかる。比較例の試験No.17およびNo.20で
は、凝固点がいずれも1300℃以上と高く、鋳造に使
用出来なかった。比較例の試験No.18およびNo.
19では、結晶析出が過多あるいは不安定であるため、
鋳型銅板温度の変動が大きく、No.19では縦割れも
発生した。
In the test in which medium carbon steel was cast at a speed of 1.1 m / min, the test No. Compared with Test No. 16 of the present invention, 11-No. In No. 15, it can be seen that all of the flaws, pinhole flaws, longitudinal cracks, and variations in the temperature of the mold copper plate are reduced, and the surface quality of the slab is improved. Test No. of the comparative example. 17 and No. In the case of No. 20, the solidification point was as high as 1300 ° C. or higher, and it was impossible to use for casting. Test No. of the comparative example. 18 and No.
In 19, since the crystal precipitation is excessive or unstable,
The temperature of the mold copper plate greatly fluctuated. In 19, a vertical crack also occurred.

【0034】[0034]

【発明の効果】本発明のモールドパウダおよびそのモー
ルドパウダを用いる本発明の連続鋳造方法の適用によ
り、鋳片表面にディプレッションまたは縦割れの発生の
ない、さらに、鋳片表層部の清浄性も良好な鋳片を得る
ことができる。
According to the mold powder of the present invention and the continuous casting method of the present invention using the mold powder, no depletion or vertical cracking occurs on the slab surface, and the cleanness of the surface layer of the slab is good. A simple slab can be obtained.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 川本 正幸 大阪府大阪市中央区北浜4丁目5番33号 住友金属工業株式会社内 Fターム(参考) 4E004 MB14 NC04  ────────────────────────────────────────────────── ─── Continuing on the front page (72) Inventor Masayuki Kawamoto 4-5-33 Kitahama, Chuo-ku, Osaka-shi, Osaka Sumitomo Metal Industries, Ltd. F-term (reference) 4E004 MB14 NC04

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】CaO、SiO2 、Al23 およびフッ
素化合物を基本成分とするモールドパウダであって、C
aOのSiO2 に対する質量%の比CaO/SiO2
1.1〜1.5であり、Al23 を5〜15質量%、
アルカリ金属を酸化物換算含有率の合計で5質量%以
下、ZrO2 を1質量%以下、TiO2 を0〜8質量
%、Fを4〜12質量%含有し、1300℃における粘
度が2〜6poise、凝固点が1100℃以上である
ことを特徴とする連続鋳造用のモールドパウダ。
1. A mold powder comprising CaO, SiO 2 , Al 2 O 3 and a fluorine compound as basic components,
The ratio CaO / SiO 2 mass% with respect to SiO 2 of aO is 1.1 to 1.5, the Al 2 O 3 5 to 15 wt%,
5 wt% of an alkali metal in a total of oxide conversion content below the ZrO 2 1 wt% or less, the TiO 2 0 to 8 wt%, and contains 4-12 wt% of F,. 2 to a viscosity at 1300 ° C. A mold powder for continuous casting, characterized in that the powder has a solidification point of 1100 ° C. or more.
【請求項2】Al23 、TiO2 およびFの含有率
が、下記(A)式を満足することを特徴とする請求項1
に記載の連続鋳造用のモールドパウダ。 2≦(Al23 )×(TiO2)≦10+15×(F)・・・(A) ここで、(Al23 ):モールドパウダ中のAl2
3 含有率(質量%) (TiO2):モールドパウダ中のTiO2 含有率(質
量%) (F):モールドパウダ中のF含有率(質量%)
2. The method according to claim 1, wherein the contents of Al 2 O 3 , TiO 2 and F satisfy the following formula (A).
3. A mold powder for continuous casting according to item 1. 2 ≦ (Al 2 O 3 ) × (TiO 2 ) ≦ 10 + 15 × (F) (A) where (Al 2 O 3 ): Al 2 O in the mold powder
( 3 ) Content (% by mass) (TiO 2 ): Content of TiO 2 in mold powder (% by mass) (F): Content of F in mold powder (% by mass)
【請求項3】請求項1または請求項2に記載のモールド
パウダを用いる連続鋳造方法であって、下記(B)式で
定義される溶鋼の化学組成Cpとモールドパウダ中のA
23 含有率との間の関係が、下記(C)式または
(D)式を満足する条件で鋳造することを特徴とする連
続鋳造方法。 Cp=C+0.02×Mn+0.04×Ni−0.01×Si +0.02×Cr+0.07×S・・・(B) ここで、C、Mn、Ni、Si、CrおよびS:溶鋼中
の含有率(質量%)|Cp−0.12|≦0.05の場
合; 5+2000×|Cp−0.12|2 ≦(Al23 )≦ 10+2000×|Cp−0.12|2 ・・・(C) |Cp−0.12|>0.05の場合; 10≦(Al23 )≦15 ・・・(D) ここで、|Cp−0.12|:Cpの値から0.12を
引いた値の絶対値 (Al23 ):モールドパウダ中のAl23 含有率
(質量%)
3. A continuous casting method using the mold powder according to claim 1 or 2, wherein a chemical composition Cp of molten steel defined by the following formula (B) and A in the mold powder are provided.
A continuous casting method characterized in that casting is performed under the condition that the relationship with the l 2 O 3 content satisfies the following formula (C) or (D). Cp = C + 0.02 × Mn + 0.04 × Ni-0.01 × Si + 0.02 × Cr + 0.07 × S (B) Here, C, Mn, Ni, Si, Cr and S: in molten steel 5 + 2000 × | Cp-0.12 | 2 ≦ (Al 2 O 3 ) ≦ 10 + 2000 × | Cp−0.12 | 2 ... When the content (mass%) | Cp−0.12 | ≦ 0.05;・ (C) When | Cp−0.12 |>0.05; 10 ≦ (Al 2 O 3 ) ≦ 15 (D) where | Cp−0.12 |: 0 from the value of Cp Absolute value of the value obtained by subtracting 12 (Al 2 O 3 ): Al 2 O 3 content in the mold powder (% by mass)
JP2000171155A 2000-06-07 2000-06-07 Mold powder and continuous casting method Expired - Lifetime JP3610885B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2000171155A JP3610885B2 (en) 2000-06-07 2000-06-07 Mold powder and continuous casting method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2000171155A JP3610885B2 (en) 2000-06-07 2000-06-07 Mold powder and continuous casting method

Publications (2)

Publication Number Publication Date
JP2001347351A true JP2001347351A (en) 2001-12-18
JP3610885B2 JP3610885B2 (en) 2005-01-19

Family

ID=18673744

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2000171155A Expired - Lifetime JP3610885B2 (en) 2000-06-07 2000-06-07 Mold powder and continuous casting method

Country Status (1)

Country Link
JP (1) JP3610885B2 (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005115653A1 (en) * 2004-05-28 2005-12-08 Ngk Insulators, Ltd. Method for forming metallic glass
JP2007130684A (en) * 2005-11-14 2007-05-31 Sumitomo Metal Ind Ltd Mold powder for continuously casting steel and continuous casting method
CN1321764C (en) * 2004-06-23 2007-06-20 青岛斯多伯格三一冶金材料有限公司 Fluorine free protecting slag for steelmaking and continuous casting and method for manufacturing same
EP2407563A1 (en) * 2010-07-13 2012-01-18 Denain Anzin Métallurgie D.A.MET Covering powder for liquid steel and method for manufacturing same
CN112756570A (en) * 2019-11-05 2021-05-07 上海梅山钢铁股份有限公司 Continuous casting start-up slag for casting peritectic steel

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105642847A (en) * 2016-01-26 2016-06-08 中南大学 Casting powder for continuous casting of low-carbon steel and application of casting powder

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005115653A1 (en) * 2004-05-28 2005-12-08 Ngk Insulators, Ltd. Method for forming metallic glass
JPWO2005115653A1 (en) * 2004-05-28 2008-03-27 日本碍子株式会社 Metal glass forming method
US7708844B2 (en) 2004-05-28 2010-05-04 Ngk Insulators, Ltd. Method of forming metallic glass
JP4693772B2 (en) * 2004-05-28 2011-06-01 日本碍子株式会社 Metal glass forming method
KR101203757B1 (en) * 2004-05-28 2012-11-21 고쿠리츠다이가쿠호진 도호쿠다이가쿠 Method for forming metallic glass
CN1321764C (en) * 2004-06-23 2007-06-20 青岛斯多伯格三一冶金材料有限公司 Fluorine free protecting slag for steelmaking and continuous casting and method for manufacturing same
JP2007130684A (en) * 2005-11-14 2007-05-31 Sumitomo Metal Ind Ltd Mold powder for continuously casting steel and continuous casting method
JP4508086B2 (en) * 2005-11-14 2010-07-21 住友金属工業株式会社 Mold powder for continuous casting of steel and continuous casting method
EP2407563A1 (en) * 2010-07-13 2012-01-18 Denain Anzin Métallurgie D.A.MET Covering powder for liquid steel and method for manufacturing same
CN112756570A (en) * 2019-11-05 2021-05-07 上海梅山钢铁股份有限公司 Continuous casting start-up slag for casting peritectic steel
CN112756570B (en) * 2019-11-05 2022-07-15 上海梅山钢铁股份有限公司 Continuous casting start-up slag for casting peritectic steel

Also Published As

Publication number Publication date
JP3610885B2 (en) 2005-01-19

Similar Documents

Publication Publication Date Title
JP5370929B2 (en) Mold flux for continuous casting of steel
JP4708055B2 (en) Mold powder for continuous casting of steel
JP4422913B2 (en) Mold powder for continuous casting of steel and continuous casting method of steel
JP2006289383A (en) Mold flux for continuous casting of steel
JP3649153B2 (en) Mold powder for continuous casting
JPH11320058A (en) Mold powder for continuous casting and continuous casting method
JP3997963B2 (en) Mold powder for continuous casting of steel
JP6674093B2 (en) Mold powder for continuous casting of steel and continuous casting method
JP4460463B2 (en) Mold powder for continuous casting of steel
JP3780966B2 (en) Continuous casting powder and continuous casting method using it
JPH0976049A (en) Flux for continuous casting of molten steel containing aluminum and continuous casting method
JP2001347351A (en) Mold powder and continuous casting method
JP2003225744A (en) Powder for continuous casting and continuous casting method using this powder
WO2011004507A1 (en) Mold flux for continuous casting of steel and method for continuous casting of steel using same
JP2006110578A (en) Mold powder for continuously casting high aluminum-containing steel and method for continuously casting high aluminum-containing steel using the powder
JP2004358485A (en) Mold flux for continuous casting of steel
JP2000158105A (en) Mold powder for continuous steel casting and continuous casting method
JPH0985404A (en) Flux for continuously casting a1-containing molten steel and continuous casting method
JP3249429B2 (en) Mold powder for continuous casting of steel
JP2003326342A (en) Mold powder for continuous casting of steel
JPH08141713A (en) Molding powder for continuous casting of steel
JP3399387B2 (en) Steel continuous casting method
JP3876917B2 (en) Steel continuous casting method
JP2000051998A (en) Method for continuously casting lead-containing steel
JPH09308951A (en) Mold powder for continuously casting steel

Legal Events

Date Code Title Description
TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20040928

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20041011

R150 Certificate of patent or registration of utility model

Free format text: JAPANESE INTERMEDIATE CODE: R150

Ref document number: 3610885

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R150

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20081029

Year of fee payment: 4

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20091029

Year of fee payment: 5

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20091029

Year of fee payment: 5

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20101029

Year of fee payment: 6

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20111029

Year of fee payment: 7

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20121029

Year of fee payment: 8

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20131029

Year of fee payment: 9

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20131029

Year of fee payment: 9

S111 Request for change of ownership or part of ownership

Free format text: JAPANESE INTERMEDIATE CODE: R313111

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20131029

Year of fee payment: 9

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

S533 Written request for registration of change of name

Free format text: JAPANESE INTERMEDIATE CODE: R313533

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

EXPY Cancellation because of completion of term