JP2003138351A - Alloying-element additive - Google Patents

Alloying-element additive

Info

Publication number
JP2003138351A
JP2003138351A JP2001367884A JP2001367884A JP2003138351A JP 2003138351 A JP2003138351 A JP 2003138351A JP 2001367884 A JP2001367884 A JP 2001367884A JP 2001367884 A JP2001367884 A JP 2001367884A JP 2003138351 A JP2003138351 A JP 2003138351A
Authority
JP
Japan
Prior art keywords
molten steel
steel
converter
shaped
scrap
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.)
Pending
Application number
JP2001367884A
Other languages
Japanese (ja)
Inventor
Katsumi Numa
勝己 沼
Hiroshi Fukuoka
浩 福岡
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.)
METTSU CORP KK
Metz Corp
Original Assignee
METTSU CORP KK
Metz Corp
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 METTSU CORP KK, Metz Corp filed Critical METTSU CORP KK
Priority to JP2001367884A priority Critical patent/JP2003138351A/en
Publication of JP2003138351A publication Critical patent/JP2003138351A/en
Pending legal-status Critical Current

Links

Landscapes

  • Treatment Of Steel In Its Molten State (AREA)
  • Carbon Steel Or Casting Steel Manufacturing (AREA)

Abstract

PROBLEM TO BE SOLVED: To provide easy-handling low-cost additives used for adding alloying elements at low-alloy steel manufacture because component additives for use in operations subsequent to a deoxidation operation in a converter should be pure and have minimal impurity content to prevent molten steel from recontamination. SOLUTION: The alloying-element additives can be obtained by subjecting sheet-like or slit-like scraps of Cr-based stainless steel, Ni-based stainless steel and Ni steel to shearing into small pieces using a shredder and are used when manufacturing low-alloy steel.

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】この発明は低合金構造用鋼等
の合金鋼を製造する際に用いられる合金元素添加材に関
するものである。より詳しくは、NiまたはCrの添加
に通常用いられるNiカソードあるいは低炭素フェロク
ローム(以下LCFeCrと記す)に取って代わるもの
で、ハンドリングが容易で、且つ安価な材料である。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an alloying element additive used in the production of alloy steel such as low alloy structural steel. More specifically, it is a material that replaces a Ni cathode or low carbon ferrochrome (hereinafter referred to as LCFeCr) that is usually used for adding Ni or Cr, is easy to handle, and is inexpensive.

【0002】以下、機械構造用ニッケルクローム鋼を例
にとって説明する。高炉より取り出された溶銑は脱硫
(S)、脱シリコン(Si)、脱リン(P)処理が施さ
れた後、転炉に装入される。転炉では溶銑中に高圧・高
速の気体酸素が吹き込まれ、所定のカーボン(C)値に
なるまで脱炭(C)が行われ溶綱が形成される。その
後、冷却材を投入するなどして所定の温度にし取鍋に移
注される。
A nickel-chromium steel for machine structure will be described below as an example. The hot metal taken out from the blast furnace is desulfurized (S), desiliconized (Si) and dephosphorized (P), and then charged into a converter. In the converter, high-pressure, high-speed gaseous oxygen is blown into the hot metal, and decarburization (C) is performed until a predetermined carbon (C) value is reached to form molten steel. Then, a coolant is added to bring the mixture to a predetermined temperature and the mixture is transferred to a ladle.

【0003】しかしこの時点での溶鋼は、多量の酸素
(O)を含有しているため取鍋への注入時、アルミ(A
l)あるいはフェロシリコン(FeSi)を投入し、脱
酸(O)が行われる。取鍋への注入が完了すると、クレ
ーンで吊り上げられ次工程である脱ガス装置(以下RH
と記す)に運ばれ、減圧下において精錬作業が行われ
る。 精錬作業とは、前述のAlあるいはFeSiによ
る脱酸作業により生じた非金属介在物の浮上除去、溶鋼
中に微量に含まれるガス(水素、窒素、酸素)の排除が
主な目的である。また同時に、溶鋼のSi,Mn,C
r,Ni等の成分の調整も行われる。RHにて使用され
るこれら成分の添加材はすでに精錬が完了した溶鋼に投
入されるため、不純物を一切含まないピュアなものであ
る。最後に冷却材等を用いて所定の温度に調節された溶
鋼は、次工程の連続鋳造機(以下CCと記す)へ運ばれ
スラブに成型される。
However, since the molten steel at this point contains a large amount of oxygen (O), it cannot be filled with aluminum (A
l) or ferrosilicon (FeSi) is added and deoxidation (O) is performed. When the injection into the ladle is completed, it is lifted up by a crane and is the degassing device in the next step (hereinafter referred to as RH
It is carried to refining work under reduced pressure. The refining work mainly aims to remove the non-metallic inclusions generated by the above-mentioned deoxidation work with Al or FeSi by floating, and to remove the gas (hydrogen, nitrogen, oxygen) contained in a trace amount in the molten steel. At the same time, the molten steel Si, Mn, C
The components such as r and Ni are also adjusted. Additives for these components used in RH are pure and do not contain any impurities because they are added to molten steel that has already been refined. Finally, the molten steel adjusted to a predetermined temperature with a coolant or the like is conveyed to a continuous casting machine (hereinafter referred to as CC) in the next step and formed into a slab.

【0004】[0004]

【発明が解決しようとする課題】以上述べてきた如く、
転炉での脱酸作業以降に使用される成分添加材は溶鋼を
再汚染から防ぐために不純物の極めて少なくピュアなも
のが用いられる。例えば、Crの添加材料として通常用
いられているLCFeCrはCr鉱石を原料として複雑
で長い作業工程を経て製造されるが、エネルギー使用
量、人件費等が嵩み高価なものとなっている。Niに関
しても全く同じことが言え、通常用いられているNiカ
ソードも極めて高価なものである。そこで、発明者等
は、高純度ではあるが高価なLCFeCr、Niカソー
ドに取って代わるハンドリングが容易で且つ安価な成分
添加材を提案するものである。
DISCLOSURE OF THE INVENTION Problems to be Solved by the Invention As described above,
As the additive material used after the deoxidation work in the converter, a pure material with very few impurities is used to prevent the molten steel from being recontaminated. For example, LCFeCr, which is usually used as a Cr addition material, is manufactured from Cr ore as a raw material through a complicated and long working process, but the amount of energy used, labor costs, etc. are high and expensive. The same can be said for Ni, and the commonly used Ni cathode is also extremely expensive. Therefore, the present inventors propose a component additive which is easy to handle and inexpensive to replace the expensive LCFeCr, Ni cathode with high purity.

【0005】[0005]

【課題を解決するための手段】まず、泥,プラスチッ
ク,紙,木片等の非金属、及び亜鉛(Zn),銅(C
u)等の非鉄金属の付着していない清浄な板状もしくは
スリット状のCr系ステンレス鋼,Ni系ステンレス鋼
あるいはニッケル鋼のスクラップを選別し、各々シュレ
ッダーにて剪断、小片化する。このようにして小片化さ
れたスクラップは、転炉あるいはRHの炉上に搬送さ
れ、炉上バンカーに貯えられ、溶鋼成分の調整時前記バ
ンカーより切り出され、LCFeCrおよび/またはN
iカソードの代替として溶鋼に投入される。
[Means for Solving the Problems] First, non-metals such as mud, plastic, paper, wood chips, and zinc (Zn), copper (C)
u) A clean plate-shaped or slit-shaped scrap of Cr-based stainless steel, Ni-based stainless steel or nickel steel on which non-ferrous metal such as u) is not attached is selected, and each is shredded and shredded by a shredder. The scrap thus crushed is conveyed to a converter or an RH furnace, stored in a furnace bunker, cut out from the bunker at the time of adjusting the molten steel composition, and is fed with LCFeCr and / or N.
It is put into molten steel as an alternative to the i cathode.

【0006】これらの小片状スクラップは転炉での脱炭
・脱酸後もしくはRHでの精錬後使用されるため不純物
を一切含まないピュアなものでなければならないことは
既に述べた通りである。又、成分値は明確で一定でなけ
ればならないことは言うまでもない。更には、炉上バン
カーにて貯え、且つ自動切り出しがスムースに行えるよ
う角のとれた丸味を帯びた形状が望ましい。
As described above, these small scraps must be pure without any impurities because they are used after decarburization and deoxidation in the converter or after refining in RH. . Also, it goes without saying that the component values must be clear and constant. Further, it is desirable to have a rounded shape with corners so that it can be stored in a furnace bunker and can be automatically cut out smoothly.

【0007】[0007]

【発明の実施の形態】以下、この発明を実施例を用いて
具体的に説明する。対象鋼種はニッケルクローム鋼、よ
り詳しくはSNC415Mでテストを行った。溶銑から
の製造工程は、(溶銑予備処理)−(転炉)−(RH)
−(CC)であり、又1チャージあたりの溶鋼量は約3
00トンであった。参考までに、SNC415Mの成分
規格を表−1に示す。
BEST MODE FOR CARRYING OUT THE INVENTION The present invention will be specifically described below with reference to embodiments. The target steel type was nickel chrome steel, more specifically SNC415M was tested. The manufacturing process from hot metal is (pre-treatment of hot metal)-(converter)-(RH)
-(CC), and the amount of molten steel per charge is about 3
It was 00 tons. For reference, the component specifications of SNC415M are shown in Table-1.

【0008】今回のテストに用いた小片状スクラップ
は、製鉄所ステンレス鋼冷延工場より副生した厚さ約
0.8mmのSUS304薄板屑をシュレッダーにかけ
小片状に加工したものであった。尚、採取したサンプル
を分析したところ化学組成は表−2に示す通りであっ
た。
The small piece scrap used in this test was a piece of SUS304 thin plate scrap having a thickness of about 0.8 mm produced as a by-product from a cold rolling mill for stainless steel at a steel mill, which was processed into a small piece with a shredder. When the collected sample was analyzed, the chemical composition was as shown in Table-2.

【0009】[0009]

【第1回テスト状況及び結果】溶銑予備処理工程より転
炉での作業完了までは全く通常と変わらないものであっ
た。転炉作業完了後、溶鋼成分のチェックがなされたの
ち、温度の確認が行われた。転炉々下に取鍋がセットさ
れると転炉を傾倒して溶鋼が取鍋に注入されたが、注入
開始約2分後アルミ(Al)が投入され脱酸が行われ
た。更に、脱酸反応が完了した時点を見計って、溶鋼の
冷却も兼ねて、炉上バンカーに貯えておいたSUS30
4小片スクラップ4,500kgが取鍋中の溶鋼めがけ
て投入された。転炉から取鍋への溶鋼注入が終了した
後、取鍋は次工程であるRHへ移送された。
[1st test status and results] From the hot metal pretreatment process to the completion of the work in the converter, there was no difference from normal. After the converter work was completed, the molten steel composition was checked and then the temperature was checked. When the ladle was set under the converter, the converter was tilted and molten steel was poured into the ladle, but about 2 minutes after the start of pouring, aluminum (Al) was charged and deoxidation was performed. Furthermore, when the deoxidation reaction was completed, the SUS30 stored in the bunker above the furnace also served to cool the molten steel.
4,500 kg of four small pieces of scrap were put on the molten steel in the ladle. After the molten steel injection from the converter to the ladle was completed, the ladle was transferred to the next step, RH.

【0010】RHへ到着後、直ちに溶鋼のサンプリング
が行われ、分析室へ送られた。精錬処理前の溶鋼組成は
表−3に示す通りであった。 そこで成分値をSNC415Mの規格に合わせるため、
下記合金鉄及びSUS304小片スクラップが炉上バン
カーより投入されたが、その量は各々次の如くであっ
た。 FeSi 870kg LCFeMn 1,660kg SUS304小片スクラップ 970kg RHでの精錬作業は通常の方法で行われ、精錬終了後、
再度サンプリングを行い分析したところ表−4に示す組
成であった。 その後温度調整がなされ、次工程であるCCへ移送され
た。
Immediately after reaching the RH, the molten steel was sampled and sent to the analysis room. The molten steel composition before the refining treatment was as shown in Table-3. Therefore, in order to match the component values to the SNC415M standard,
The following ferroalloys and SUS304 small piece scraps were charged from the furnace bunker, and the amounts were as follows. FeSi 870 kg LCFeMn 1,660 kg SUS304 small piece scrap 970 kg Refining work with RH is carried out by a usual method.
When it was sampled again and analyzed, it had the composition shown in Table 4. After that, the temperature was adjusted and transferred to the next step, CC.

【0011】[0011]

【第2回テスト状況及び結果】転炉作業及び取鍋への溶
鋼注入までは第1回テストと同じであったが、注入開始
約2分後フェロシリコン(FeSi)が投入され、脱酸
が行われた。又、脱酸反応が完了した頃を見計って、炉
上バンカーよりSUS304小片スクラップ5,000
kgが取鍋内溶鋼中に投入された。溶鋼注入が完了した
後、取鍋は次工程のRHへ移送された。
[Second test status and results] The same operation as the first test was performed up to the converter operation and the injection of molten steel into the ladle, but about 2 minutes after the start of injection, ferrosilicon (FeSi) was added and deoxidation was performed. It was conducted. In addition, when the deoxidation reaction was completed, SUS304 small piece scrap 5,000 from the furnace bunker
kg was put into the molten steel in the ladle. After the molten steel injection was completed, the ladle was transferred to the RH in the next step.

【0012】RH到着後サンプリングが行われ、分析室
へ送られた。精錬作業前の溶鋼組成は表−5に示される
如くであった。 分析値判明後、直ちに炉上バンカーより下記の合金鉄及
びSUS304小片スクラップが投入されたが、使用量
は各々以下の通りであった。 FeSi 870kg LCFeMn 1,650kg SUS304小片スクラップ 520kg その後精錬作業は通常の方法で行われたが、作業完了
後、溶鋼成分の分析を行ったところ表−6に示す通りで
あった。 規格を充分満たしているため温度調整など通常の作業が
行われた後、次工程であるCCへ移送された。
After arrival at the RH, sampling was performed and sent to the analysis room. The composition of the molten steel before the refining work was as shown in Table-5. Immediately after the analysis value was determined, the following ferroalloys and SUS304 small piece scraps were charged from the furnace bunker, but the amounts used were as follows. FeSi 870 kg LCFeMn 1,650 kg SUS304 small piece scrap 520 kg After that, the refining work was performed by the usual method, but after the work was completed, the analysis of molten steel components was as shown in Table-6. Since it satisfied the standard sufficiently, it was transferred to CC, which is the next step, after normal operations such as temperature adjustment were performed.

【0013】[0013]

【第3回テスト状況及び結果】転炉作業及び取鍋での脱
酸までは第2回テストと変わらない作業が行われた。脱
酸反応完了後、炉上バンカーよりSUS304小片スク
ラップ6,000kgが溶鋼中めがけて投入された。取
鍋への溶鋼移注完了後、次工程のRHへ運ばれた。
[Third test status and results] The same work as the second test was performed until the converter work and deoxidation in the ladle. After the completion of the deoxidation reaction, 6,000 kg of SUS304 small piece scrap was thrown into the molten steel from the furnace bunker. After the molten steel transfer to the ladle was completed, it was transferred to the RH in the next process.

【0014】RH到着後、通常通り溶鋼成分の分析が行
われた。溶鋼組成は表−7に示すとおりであった。 分析値判明後、直ちに炉上バンカーより下記の合金鉄が
切り出され、溶鋼中に投入された。合金鉄の使用量は各
々以下の如くであった。 FeSi 870kg LCFeMn 1,670kg SUS304小片スクラップ 120kg その後通常作業が行われたが、CC移送前の溶鋼成分は
以下の通りであり、規格を充分満たすものであった。
After the arrival of the RH, the analysis of molten steel components was conducted as usual. The molten steel composition was as shown in Table-7. Immediately after the analysis value was found, the following ferroalloys were cut out from the furnace bunker and put into molten steel. The amount of iron alloy used was as follows. FeSi 870 kg LCFeMn 1,670 kg SUS304 small piece scrap 120 kg After that, normal work was carried out, but the molten steel components before CC transfer were as follows, which satisfied the standards sufficiently.

【0015】[0015]

【発明の効果】かくして、この発明の小片スクラップを
通常の装置を用いて、通常の作業を行えば、製鋼原価を
簡単に且つ大幅に削減することが出来る。
As described above, if the small piece scrap of the present invention is subjected to the normal work by using the normal equipment, the steelmaking cost can be easily and significantly reduced.

Claims (5)

【特許請求の範囲】[Claims] 【請求項 1】 Ni及びCrを含有する板状もしくは
スリット状のスクラップをシュレッダーによりせん断・
小片化した製鋼用合金元素添加材。
1. A plate-shaped or slit-shaped scrap containing Ni and Cr is sheared by a shredder.
A small piece of alloying element additive for steelmaking.
【請求項 2】 板状もしくはスリット状のスクラップ
が、Crを15%以上含有するCr系ステンレス鋼であ
ることを特徴とする請求項 1.に記載の合金元素添加
材。
2. The plate-shaped or slit-shaped scrap is Cr-based stainless steel containing 15% or more of Cr. The alloying element-added material described in.
【請求項 3】 板状もしくはスリット状のスクラップ
がCrを16%以上、Niを6%以上含有するNi系ス
テンレス鋼であることを特徴とする請求項1.に記載の
元素添加材。
3. The plate-shaped or slit-shaped scrap is Ni-based stainless steel containing Cr of 16% or more and Ni of 6% or more. Element addition material described in.
【請求項 4】 板状もしくはスリット状のスクラップ
がNiを8%以上含有するNi鋼であることを特徴とす
る請求項 1.記載の合金元素添加材。
4. The plate-shaped or slit-shaped scrap is Ni steel containing 8% or more of Ni. The alloying element-added material described.
【請求項 5】 最大長さが300mm以下であること
を特徴とする請求項2.3.および4.記載の合金元素
添加材。
5. The maximum length is 300 mm or less, 2.3. And 4. The alloying element-added material described.
JP2001367884A 2001-10-29 2001-10-29 Alloying-element additive Pending JP2003138351A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2001367884A JP2003138351A (en) 2001-10-29 2001-10-29 Alloying-element additive

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2001367884A JP2003138351A (en) 2001-10-29 2001-10-29 Alloying-element additive

Publications (1)

Publication Number Publication Date
JP2003138351A true JP2003138351A (en) 2003-05-14

Family

ID=19177567

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2001367884A Pending JP2003138351A (en) 2001-10-29 2001-10-29 Alloying-element additive

Country Status (1)

Country Link
JP (1) JP2003138351A (en)

Similar Documents

Publication Publication Date Title
US9556498B2 (en) Method for producing spheroidal graphite cast iron and vehicle component using said spheroidal graphite cast iron
RU2527569C2 (en) CONTROL OVER ULTRA-LOW TITANIUM CONTENT IN ULTRA-LOW-CARBON Al-Si KILLED STEEL
US9512498B2 (en) Process for producing spheroidal-graphite cast iron, and spheroidal-graphite cast iron member obtained from said spheroidal-graphite cast iron
CN110273105B (en) High-speed tool steel and preparation method thereof
CN105567907A (en) Method for controlling plastic inclusions of austenitic stainless steel
CN110004371B (en) Wear-resistant steel and smelting method
JP6990337B1 (en) Ni-based alloy with excellent surface properties and its manufacturing method
EP4067512A1 (en) Hot stamp molded product and steel sheet for hot stamping
CN114107601A (en) Method for refining rare earth inclusions in steel by magnesium pretreatment
CN101168824A (en) Leadless easy-cutting steel for medium-hard tooth face heavy load gear wheel and preparation method thereof
CN101020942A (en) Molten steel deoxygenating agent and its prepn
CN108385035B (en) Method for refining 14Cr1Mo alloy steel outside furnace by adopting premelted refining slag
CN113046616B (en) Stainless steel excellent in surface properties and method for producing same
US7704450B2 (en) High-purity ferroboron, a mother alloy for iron-base amorphous alloy, an iron-base amorphous alloy, and methods for producing the same
CN116806273A (en) Nickel alloy with excellent surface properties and method for producing same
JP2003138351A (en) Alloying-element additive
JP2003286533A (en) Processes for producing highly pure ferroboron, mother alloy for iron-based amorphous alloy and iron-based amorphous alloy
CN115491569B (en) Production method of non-oriented silicon steel and non-oriented silicon steel
CN115323288B (en) Preparation method of chalcogenide free-cutting hot-work die steel CX2344
CN115852272B (en) Tellurium-containing high-speed steel and preparation method thereof
Panov et al. Influence of the Degree of Oxidation of Magnesium Master Alloys on the Mechanical Properties of Nodular Irons
CN116194235A (en) Method for producing cast sheet
Redeker et al. Metallurgical methods for the production of steels with high manganese contents in the range of 12 to 25% wt,[in]
CN114981460A (en) Ferritic stainless steel
JP2002206144A (en) Fe-Ni BASED ALLOY HAVING EXCELLENT SURFACE PROPERTY AND PRODUCTION METHOD THEREFOR

Legal Events

Date Code Title Description
RD02 Notification of acceptance of power of attorney

Free format text: JAPANESE INTERMEDIATE CODE: A7422

Effective date: 20040812

A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20041019

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20051228

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20060131

A02 Decision of refusal

Free format text: JAPANESE INTERMEDIATE CODE: A02

Effective date: 20060608