JPS5852412A - Dephosphorizing method for molten iron - Google Patents

Dephosphorizing method for molten iron

Info

Publication number
JPS5852412A
JPS5852412A JP14971481A JP14971481A JPS5852412A JP S5852412 A JPS5852412 A JP S5852412A JP 14971481 A JP14971481 A JP 14971481A JP 14971481 A JP14971481 A JP 14971481A JP S5852412 A JPS5852412 A JP S5852412A
Authority
JP
Japan
Prior art keywords
dephosphorization
hot metal
decarburization
molten iron
solid
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
JP14971481A
Other languages
Japanese (ja)
Inventor
Hiroyuki Katayama
裕之 片山
Masatoshi Kuwabara
桑原 正年
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
Nippon Steel 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 Nippon Steel Corp filed Critical Nippon Steel Corp
Priority to JP14971481A priority Critical patent/JPS5852412A/en
Publication of JPS5852412A publication Critical patent/JPS5852412A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21CPROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
    • C21C1/00Refining of pig-iron; Cast iron
    • C21C1/02Dephosphorising or desulfurising

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Refinement Of Pig-Iron, Manufacture Of Cast Iron, And Steel Manufacture Other Than In Revolving Furnaces (AREA)

Abstract

PURPOSE:To accelerate dephosphorization and to suppress decarburization in the stage of dephosphorizing molten iron by blowing of a coal base flux and an oxidative gas into said molten iron, by blowing a carbonaceous solid simultaneously into the molten iron. CONSTITUTION:A mixture of a coal base flux and an oxidative gas supplied from a flux supplying device 8 and an oxidative gas supplying device 9 is blown through the central part of an immersion lance 5 into the molten iron 3 contained in a pan 1. At the same time, a mixture of a solid carbonaceous material such as coke powder and a carrier gas supplied from a solid carobanaceous material supplying device 7 and a solid carbonaceous material carrier gas supplying device 6 is blown through the lance 5 into the iron 3. Then dephosphorization is accelerated and the C% at the end point of the dephoshorization is maintained at a high grade.

Description

【発明の詳細な説明】 本発明は溶銑を転炉外で脱リン処理するための方法に関
する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for dephosphorizing hot metal outside a converter.

従来、転炉内で酸素吹錬することにより脱炭と脱リンを
行う製鋼法が用いられてきたが、最近、脱リンをあらか
じめ転炉外で行っておき、転炉は主として脱炭だけを行
う方法の利点が明らかにされ、各種の転炉外脱リンリン
法が検討されている。この場合、脱リンの原理は石灰な
どの塩基性7う。
Conventionally, steelmaking methods have been used in which decarburization and dephosphorization are carried out by oxygen blowing in a converter, but recently dephosphorization has been performed outside the converter in advance, and the converter mainly performs only decarburization. The advantages of this method have been clarified, and various methods of dephosphorization outside the converter are being investigated. In this case, the principle of dephosphorization is based on basic substances such as lime.

クスと、酸素ガスや酸化鉄などの酸化剤、および螢石な
どの媒溶剤を加えて、溶銑中のリンを酸化した後、リン
酸カルシウムとしてスラグ中に固定する方法であり、従
来、転炉内で行われてきた脱リン方法と似ている。異な
っているのは、脱炭がおこる条件(すなわち、酸素が十
分に供給できる)下で脱リンを考えればよかったのに対
し、転炉外脱リンにおいては脱炭の抑制が重要な課題に
なることである。何故ならば、転炉外脱リンにおころ脱
炭量が多いと、発生ガスの処理のために犬がかりな設備
を要し設備費を高くすること、また、転炉で回収できる
高CO濃度のガス量を減少せしめるためである。したが
って、これまで炉外脱リン処理時の脱炭を抑制して処理
後の溶銑0%を低下せしめないために種々の方法の開発
が行われているが、現時点では90%の脱リンを行う場
合には、Cが絶対値として0゜7〜0.9%、あるいは
それ以上低下している。すなわち溶銑に含まhる4チ強
のCのうち、15〜20チが脱リン処理中に低下し、そ
の際生成するCO濃度の低いガスが回収できずに放散さ
れることになる。したがって、脱リン処理を少量の低リ
ン鋼種のみならず全NMに適用することとすれば製鉄所
のエネルギーバランス上問題になる。また、溶銑処理後
のpが低いと、後続の転炉での発熱量が減少するので、
脱炭後の溶鋼温度が規定されているとすれば脱リン処理
後の溶銑温度はそれだけ高めておくことが必要になる。
This is a method of oxidizing phosphorus in hot metal by adding oxidizing agents such as oxygen gas and iron oxide, and solvents such as fluorite to fixing it in slag as calcium phosphate. It is similar to the dephosphorization method that has been used. The difference is that dephosphorization only needs to be considered under conditions where decarburization occurs (that is, sufficient oxygen can be supplied), whereas in dephosphorization outside the converter, suppressing decarburization is an important issue. That's true. This is because if the amount of decarburization in the converter is large during dephosphorization outside the converter, extensive equipment is required to treat the generated gas, which increases equipment costs, and the CO concentration that can be recovered in the converter is high. This is to reduce the amount of gas. Therefore, various methods have been developed to suppress decarburization during outside-furnace dephosphorization treatment and prevent the 0% level of hot metal after treatment; however, at present, 90% dephosphorization is required. In some cases, the absolute value of C has decreased by 0.7 to 0.9% or more. That is, of the 4+ h C contained in the hot metal, 15 to 20 C decreases during the dephosphorization process, and the gas produced at that time with a low CO concentration cannot be recovered and is dissipated. Therefore, if dephosphorization treatment is applied not only to a small amount of low-phosphorus steel types but also to all NM, it will pose a problem in terms of the energy balance of the steelworks. In addition, if the p value after hot metal treatment is low, the amount of heat generated in the subsequent converter will decrease, so
If the temperature of molten steel after decarburization is specified, the temperature of molten metal after dephosphorization must be increased accordingly.

しかし、よく知られているように処理温度が高いことは
脱リンにとりては(特に平衡的に)不利である。
However, as is well known, high treatment temperatures are disadvantageous for dephosphorization (especially in terms of equilibrium).

本発明は以上のような事情に鑑み、脱リン処理時の脱炭
反応を抑制して処理後のC含有量を高めるための方法を
種々検討の結果得られたもので、その特命とする処は、
石灰系フラックスと酸化性ガスを溶銑中に吹き込んで脱
リン処理を行うに際し、同時にコークス粉のような炭素
質固体を溶銑中に吹き込むことを特徴とする溶銑の脱リ
ン方法にある。
In view of the above-mentioned circumstances, the present invention was obtained as a result of various studies on a method for suppressing the decarburization reaction during dephosphorization treatment and increasing the C content after treatment, and its special purpose is to suppress the decarburization reaction during dephosphorization treatment. teeth,
A hot metal dephosphorization method characterized by blowing a carbonaceous solid such as coke powder into the hot metal at the same time when performing dephosphorization treatment by blowing lime-based flux and oxidizing gas into the hot metal.

以下、具体的な実施例によって詳細に説明する。Hereinafter, a detailed explanation will be given using specific examples.

第1図は本発明を実施するための設備の1例を□ 示す。溶銑脱リンは設備を極力簡素化するという観点か
ら、処理すべき溶銑は高炉、転炉間を運搬するための容
器、例えば鍋やトーピードカーに収めた状態で処理され
る。第1図は鍋を用いた場合である。鍋1に収められた
溶銑5中に、フラックス供給装置8および酸化性ガス供
給装置9から供給されるフラックスと酸化性ガスの混合
物が耐火物被覆した浸漬ランス6の中心部を通して吹込
まれる。
FIG. 1 shows an example of equipment for implementing the present invention. In hot metal dephosphorization, from the viewpoint of simplifying equipment as much as possible, the hot metal to be treated is treated in a container for transporting between the blast furnace and the converter, such as a pot or a torpedo car. Figure 1 shows the case using a pot. A mixture of flux and oxidizing gas supplied from a flux supply device 8 and an oxidizing gas supply device 9 is blown into the hot metal 5 contained in the ladle 1 through the center of a refractory-coated immersion lance 6.

フラックスとしては塩基性のもので最も安価な石灰(C
aOあるいはCaCO3)を主成分とするものを対象に
して述べる。フラックスとしてはそのほか酸化剤、媒溶
剤として酸化鉄、螢石などを加えることが望ましい。酸
化性ガスとしては、酸素ガスを主成分とするが一部をC
O2やN2などに置き換えられていてもよい。酸化性ガ
スは溶銑に酸素を供給して溶銑中のリンを酸化するとと
もに、生成した酸化鉄が石灰に作用して滓化を促進する
作用をする。
As a flux, lime (C
The following will focus on those whose main component is aO or CaCO3). In addition to the flux, it is desirable to add iron oxide, fluorite, etc. as an oxidizing agent and a solvent. The main component of the oxidizing gas is oxygen gas, but some of it is carbon.
It may be replaced with O2, N2, etc. The oxidizing gas supplies oxygen to the hot metal to oxidize phosphorus in the hot metal, and the generated iron oxide acts on lime to promote slag formation.

このように、石灰系フラックスと酸化性ガスを溶銑中に
吹き込んで睨リンを行うに際し、本発明の特徴は浸漬ラ
ンス5を通して石灰系フラックスや酸化性ガスと同時に
コークス粉のような炭素質固体を吹込むことである。そ
のための一方法は浸漬ランスは二重管とし、中心部から
は前述のように石灰・系フラックスと酸化性ガスを吹き
込み、外側の管からはコークス粉などの炭素質固体を、
N2のような不活性ガスあるいは炭化水素ガスをキャリ
ヤとして溶銑中に吹き込む。なお炭素質固体の供給は、
溶銑のSiが0.2%以下であるときに開始することが
望ましい。その理由は、Sl>0.1%では炭素質固体
の供給を行わなくても脱炭はおこりにくいこと、また溶
銑温度が低い場合に5i)0.2チで炭素質固体の供給
を行うとキッシュグラファイトの生成がおこるためであ
る。81<0.2%では脱炭がおこりやすくなるので、
脱炭抑制のために炭素質固体の供給は必要であり、かつ
、キック。
As described above, when performing glazing by blowing lime-based flux and oxidizing gas into hot metal, the feature of the present invention is that carbonaceous solids such as coke powder are injected simultaneously with lime-based flux and oxidizing gas through the immersion lance 5. It's about instilling. One way to do this is to use a double-pipe immersion lance, in which lime/based flux and oxidizing gas are blown into the center as described above, and carbonaceous solids such as coke powder are blown into the outer pipe.
An inert gas such as N2 or a hydrocarbon gas is blown into the hot metal as a carrier. The supply of carbonaceous solids is as follows:
It is desirable to start when the Si content of the hot metal is 0.2% or less. The reason for this is that when Sl > 0.1%, decarburization is difficult to occur even if carbonaceous solids are not supplied, and when the hot metal temperature is low, if carbonaceous solids are supplied at 5i) 0.2%. This is because formation of quiche graphite occurs. When 81<0.2%, decarburization tends to occur, so
Supply of carbonaceous solids is necessary and kick-starting to suppress decarburization.

グラファイト生成がおこる心配もない。There is no need to worry about graphite formation.

脱リン率 第2図は脱リン促進、脱炭抑制効果(脱與奮で表わす)
と、炭素質固体の適性供給量の関係を示す。この場合、
脱炭量ΔCは処理前、後におけるC分析値: C3+C
(と吹込んだ炭素分の100チが溶銑に加炭されたとし
た時のCアップti:ΔC2(4)から、式 %式%(1) により計算したものである。なお、炭素質固体としては
最も安価に入手できるコークス粉(1謂φ以下)を用い
た。また石灰の原単位#′11skq/l 溶銑で一定
とし、02がス供給量は2 Nnt’/l 、 4 N
m”/lの2水準とした。
Dephosphorization rate Figure 2 shows the effect of promoting dephosphorization and suppressing decarburization (represented by dephosphorization)
and the appropriate supply amount of carbonaceous solids. in this case,
Decarburization amount ΔC is C analysis value before and after treatment: C3+C
(It is calculated from the formula % formula % (1) from the C upti: ΔC2 (4) when 100 g of the injected carbon is carburized into hot metal. As a carbonaceous solid The most inexpensively available coke powder (less than 1 so-called φ) was used.Also, the unit of lime was constant #'11skq/l hot metal, and the amount of sulfur supplied in 02 was 2Nnt'/l, 4N
There were two levels: m''/l.

酸化精錬である脱リン処理において同時に炭素( 春固体を吹込むことは、従来の常識に反する方法である
が、第2図から適性延を選定すれば、脱リン促進・脱炭
抑制が可能になることがわかる。その理由としては次の
ようなことがあげられる。
Injecting carbon (spring solid) at the same time during the dephosphorization process, which is oxidation refining, is contrary to conventional wisdom, but if the appropriate amount of carbon is selected from Figure 2, dephosphorization can be promoted and decarburization can be suppressed. The reasons for this are as follows.

(1)酸化付ガス吹込み点近傍の溶銑温度を、炭素質固
体の顕熱および溶解熱(いずれも吸熱)によって低下す
る。これは脱炭反応を抑制するととおよびその結果とし
て酸素ポテンシャルを篩め、脱リンに有利な条件を作る
(1) The temperature of hot metal near the oxidizing gas injection point is lowered by the sensible heat and heat of dissolution (both are endothermic) of the carbonaceous solid. This suppresses the decarburization reaction and, as a result, screens the oxygen potential, creating conditions favorable for dephosphorization.

(1リ 9〉4%では9が高いほど溶存酸素レベルは高
くなり脱リンに有利になる。また9が高いほどリンの活
情係数が大になり、いずれも脱リン反応の進行に有利に
なる。
(1 Li 9> At 4%, the higher 9 is, the higher the dissolved oxygen level is, which is advantageous for dephosphorization. Also, the higher 9 is, the greater the phosphorus activation coefficient is, both of which are advantageous for progress of dephosphorization reaction. Become.

(i)  炭素質固体としてコークスのように脈石分を
伴うものを吹き込んだ場合、溶鋼中に残留した脈石物が
吹込まれた石灰の滓化を促進することにより悦リン反応
を促進する。
(i) When a carbonaceous solid with gangue content, such as coke, is injected, the gangue content remaining in the molten steel promotes the slag formation of the injected lime, thereby promoting the Yue-rin reaction.

GV)  炭素質固体による吹込みノズル先端の冷却。GV) Cooling of the blow nozzle tip with carbonaceous solid.

保護作用により、吹込み条件が安定するために脱リンに
有利になる。
The protective effect stabilizes the blowing conditions, which is advantageous for dephosphorization.

このように脱炭抑制(脱脚速度の低減、脱リン促進によ
る脱リン処理時間減少による脱炭素の減少)が行われる
とともに、わずかながらおころ脱炭を、炭素質固体吹込
みによる加炭によって補うために、脱リン処理終了時点
のC%を高位に保つことができる。その結果として脱炭
後の溶鋼温度が規定されている場合、脱リン処理終りの
溶銑温度を低下できることになり、さらに脱リン促進・
脱炭抑制ができるようになる。
In this way, decarburization is suppressed (decarburization is reduced by reducing dephosphorization speed and dephosphorization processing time is reduced by promoting dephosphorization), and a small amount of decarburization is also achieved by carburizing by injecting carbonaceous solids. To compensate, the C% at the end of the dephosphorization process can be maintained at a high level. As a result, if the temperature of molten steel after decarburization is specified, the temperature of molten metal at the end of dephosphorization can be lowered, further promoting dephosphorization and
It becomes possible to suppress decarburization.

実施例 第1図に示す装置において、次の条件で溶銑にε灰系フ
ラ、クス、酸化性ガス、コークス粉の吹込みを行い税リ
ンを行った。
EXAMPLE In the apparatus shown in FIG. 1, phosphorus was carried out by injecting epsilon ash-based fur, cous, oxidizing gas, and coke powder into hot metal under the following conditions.

処理後の溶銑の成分・温度は次の通りであった。The components and temperature of the hot metal after treatment were as follows.

吹き込んだコークス粉が全量、一旦、溶銑についたと仮
定すれば、実質の脱炭量は0.05%であおった・ なお、上記の条件のうち、コークス粉の吹込みだけを除
いた処理を行った結果、脱炭量は0.8チた。コークス
粉の添加により脱リン促進・脱炭抑制の効果があること
が認められる。
Assuming that all of the injected coke powder has once attached to the hot metal, the actual amount of decarburization was 0.05%. Note that among the above conditions, only the injection of coke powder was excluded. As a result, the amount of decarburization was 0.8 inches. It is recognized that the addition of coke powder has the effect of promoting dephosphorization and suppressing decarburization.

以上のように、本発明は石灰系フラ、りによる浴銑脱す
/処理において、同時に炭素質固体を吹込むという新し
い手法を導入することにより、溶銑脱リン促進・脱炭抑
制の効果を得ることができ結果的に溶銑脱リン工程−脱
炭工程の組合せからなる製鋼プロセスを合理的なものに
することができるので、工業的な効果が大きい。
As described above, the present invention achieves the effect of promoting hot metal dephosphorization and suppressing decarburization by introducing a new method of injecting carbonaceous solids at the same time in bath metal desorption/treatment using lime-based flaring. As a result, the steelmaking process consisting of the combination of the hot metal dephosphorization process and the decarburization process can be rationalized, which has great industrial effects.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は本発明を、溶銑鍋を用いて行う場合の設備の1
例を示す説明図、第2図は脱リン促進・体(コークス)
の供給量の関係を示す図である。 1:鍋、2:フリーボード、3:溶銑、4:7一ド、5
:浸漬ランス、6:固体炭素質搬送ガス供給装置、7:
固体炭素質供給装置、8:フラックス供給装置、9:酸
化性ガス供給装置、10:副材投入装置、11′:気泡
Figure 1 shows one of the facilities for carrying out the present invention using a hot metal ladle.
An explanatory diagram showing an example, Figure 2 is a dephosphorization promotion/body (coke)
FIG. 1: Pot, 2: Freeboard, 3: Hot metal, 4: 7-do, 5
: Immersion lance, 6: Solid carbonaceous carrier gas supply device, 7:
Solid carbonaceous supply device, 8: Flux supply device, 9: Oxidizing gas supply device, 10: Sub-material charging device, 11': Air bubbles.

Claims (1)

【特許請求の範囲】[Claims] 石灰系フラックスと酸化性ガスを溶銑中に吹き込んで脱
リン処理を行うに際し、同時にコークス粉のような炭素
質固体を溶銑中に吹き込むことを特徴とする溶銑の脱リ
ン方法。
A hot metal dephosphorization method characterized by blowing a carbonaceous solid such as coke powder into the hot metal at the same time as performing dephosphorization treatment by blowing lime-based flux and oxidizing gas into the hot metal.
JP14971481A 1981-09-22 1981-09-22 Dephosphorizing method for molten iron Pending JPS5852412A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14971481A JPS5852412A (en) 1981-09-22 1981-09-22 Dephosphorizing method for molten iron

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14971481A JPS5852412A (en) 1981-09-22 1981-09-22 Dephosphorizing method for molten iron

Publications (1)

Publication Number Publication Date
JPS5852412A true JPS5852412A (en) 1983-03-28

Family

ID=15481211

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14971481A Pending JPS5852412A (en) 1981-09-22 1981-09-22 Dephosphorizing method for molten iron

Country Status (1)

Country Link
JP (1) JPS5852412A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59211519A (en) * 1983-05-18 1984-11-30 Nisshin Steel Co Ltd Production of low p-containing chromium steel
JP2005213602A (en) * 2004-01-30 2005-08-11 Jfe Steel Kk Dephosphorizing treatment method for molten iron

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59211519A (en) * 1983-05-18 1984-11-30 Nisshin Steel Co Ltd Production of low p-containing chromium steel
JPS6213405B2 (en) * 1983-05-18 1987-03-26 Nitsushin Seiko Kk
JP2005213602A (en) * 2004-01-30 2005-08-11 Jfe Steel Kk Dephosphorizing treatment method for molten iron
JP4513340B2 (en) * 2004-01-30 2010-07-28 Jfeスチール株式会社 Hot metal dephosphorization method

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