Deprecated: The each() function is deprecated. This message will be suppressed on further calls in /home/zhenxiangba/zhenxiangba.com/public_html/phproxy-improved-master/index.php on line 456
JPS5838483B2 - Method for suction removal of hot metal processing slag - Google Patents
[go: Go Back, main page]

JPS5838483B2 - Method for suction removal of hot metal processing slag - Google Patents

Method for suction removal of hot metal processing slag

Info

Publication number
JPS5838483B2
JPS5838483B2 JP3764281A JP3764281A JPS5838483B2 JP S5838483 B2 JPS5838483 B2 JP S5838483B2 JP 3764281 A JP3764281 A JP 3764281A JP 3764281 A JP3764281 A JP 3764281A JP S5838483 B2 JPS5838483 B2 JP S5838483B2
Authority
JP
Japan
Prior art keywords
slag
treatment
hot metal
removal
simultaneous
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
Application number
JP3764281A
Other languages
Japanese (ja)
Other versions
JPS57152406A (en
Inventor
久 松永
昭喜 南
征三 峰雪
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 JP3764281A priority Critical patent/JPS5838483B2/en
Priority to AU81512/82A priority patent/AU527082B2/en
Priority to BR8201399A priority patent/BR8201399A/en
Priority to EP82301304A priority patent/EP0060706A1/en
Publication of JPS57152406A publication Critical patent/JPS57152406A/en
Publication of JPS5838483B2 publication Critical patent/JPS5838483B2/en
Expired 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
    • C21C7/00Treating molten ferrous alloys, e.g. steel, not covered by groups C21C1/00 - C21C5/00
    • C21C7/0087Treatment of slags covering the steel bath, e.g. for separating slag from the molten metal

Landscapes

  • Chemical & Material Sciences (AREA)
  • Analytical Chemistry (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)

Description

【発明の詳細な説明】 この発明は溶銑の分割精錬にお〜・て、脱P又は同時脱
S、脱P処理時に生成したスラグの流動性を高め、吸引
式スラグ、クリーナーによる排滓を容易にすることを目
的としたものである。
Detailed Description of the Invention This invention improves the fluidity of the slag generated during the deP, simultaneous deS, and deP treatment in the partial refining of hot metal, making it easier to remove the slag using a suction type slag or cleaner. The purpose is to

近年、転炉による一括精錬に代えて溶銑の分割精錬法が
盛んに実施される様になって来た。
In recent years, instead of batch refining using a converter, a method of split refining of hot metal has been widely implemented.

その基本的処理パターンは、溶銑を先づ脱Siして排滓
し、しかるのち脱P又は同時脱S、脱P後排滓し、その
後酸素吹錬により仕上精錬するものである。
The basic processing pattern is to first remove Si from the hot metal and then slag it, then remove P or simultaneously remove S, remove P and then slag, and then finish it by oxygen blowing.

溶銑を脱Si後排滓し、同時に脱S、脱Pする方法は、
既に特開昭55−94415号により提案されている。
The method of removing slag from hot metal and removing S and P at the same time is as follows:
This has already been proposed in Japanese Patent Application Laid-Open No. 55-94415.

脱Si処理は、基本的には溶銑浴中へ酸素(気散又は固
酸若しくは双方の併用)を供給し、溶銑中のSiをSi
O2として除去する方法であり、生成スラグはSiO2
含有量の高いものである。
The Si removal process basically involves supplying oxygen (vaporized or solid acid, or a combination of both) into the hot metal bath to remove Si in the hot metal.
This method removes the slag as O2, and the generated slag is SiO2.
It has a high content.

一方上記同時脱S、脱P処理としてはCa O−Cao
12/KCl、系の処理剤を用い酸素(気散又は固酸
若しくは双方の併用)を供給して処理を行なうものであ
るが、いづれにしても効率的に脱Pを行なうためには処
理スラグの塩基度(Cab/5in)を3.5以上、T
、Feを15俤以下とすることが望ましL・。
On the other hand, as the simultaneous de-S and de-P treatment, Ca O-Cao
The treatment is carried out by using a 12/KCl-based treatment agent and supplying oxygen (vaporized or solid acid, or a combination of both). Basicity (Cab/5in) of 3.5 or more, T
, it is desirable that the Fe content be 15 or less L.

一方近年かよる処理後のスラグを排出する方法として吸
引式のスラグ、クリーナーが出現し、これによりスラグ
の除去作業が非常に合理的になった。
On the other hand, in recent years, suction-type slag cleaners have appeared as a method for discharging slag after treatment, and this has made the slag removal work very streamlined.

所が上記の処理スラグは、塩基度はある程度高く、一方
、T。
However, the above-mentioned treated slag has a certain degree of basicity, but on the other hand, T.

Feは低い方が望ましいので処理後のスラグは流動性に
乏しく、上記吸引式スラグ、クリーナーによるスラグの
排出が円滑にいかず、長時間を要するか或L・は旧来の
掻出し法等の非合理的な方法によらざるを得なかった。
Since it is desirable that the Fe content be lower, the slag after treatment has poor fluidity, and the suction type slag or cleaner does not discharge the slag smoothly and takes a long time, or the old scraping method is irrational. I had no choice but to use a method.

この発明は、上記の点にかんがみ、脱P処理後のスラグ
又は同時脱S、脱P処理後のスラグの流動性を高め吸引
式スラグ、クリーナーによるスラグの排出を容易に可能
としたものである。
In view of the above points, this invention improves the fluidity of slag after P dephosphorization treatment or simultaneous desulfurization treatment, or slag after P deP treatment, making it possible to easily discharge slag using a suction type slag or cleaner. .

以下本発明の内容を詳・しく説明する。The contents of the present invention will be explained in detail below.

先づ本発明が対象とする処理は、溶銑の脱Si処理後引
続〜゛て行なう脱P処理又は同時脱S、脱P処理である
First, the treatment targeted by the present invention is a deP treatment performed sequentially after the deSi treatment of hot metal, or a simultaneous deS or deP treatment.

これは両処理共に脱P効率を高めるためには、処理スラ
グの塩基度は高(、T 、 Feは低い方が望ましく、
処理後の流動性が乏しいためであり、とのスラグの流動
性を高めるのがこの発明の目的である。
This is because in order to increase the dephosphorization efficiency in both treatments, it is desirable that the basicity of the treated slag is high (lower T, Fe, etc.).
This is because the fluidity of the slag after treatment is poor, and the purpose of this invention is to improve the fluidity of the slag.

次に本発明はスラグ流動性向上剤として、脱Si処理ス
ラグな用いるものである。
Next, the present invention uses slag treated to remove Si as a slag fluidity improver.

既に述べた如く脱Si処理は溶銑中のSiを酸化してS
iO2として脱Siするもので、生成スラグ中のS i
02量は非常に多い。
As already mentioned, the Si removal treatment oxidizes the Si in the hot metal and converts it into S.
Si is removed as iO2, and Si in the generated slag
02 amount is very large.

従来この脱Siスラグ&東例えば高炉原料等に再利用す
ることが一部で提案されているが、本発明では、スラグ
の塩基度が低くなればスラグの流動性が向上することに
着目し、この高さSiO2含有スラグを脱P処理のスラ
グ、同時脱S、脱P処理のスラグに添加し滓化すること
により同スラグの塩基度を低め、その流動性を向上させ
るものである。
Conventionally, some proposals have been made to reuse this Si-free slag & gas, for example, as raw material for blast furnaces, but in the present invention, we focus on the fact that the fluidity of slag improves when the basicity of slag is lowered. By adding this high SiO2-containing slag to the slag for deP treatment, simultaneous desulfurization, and slag for deP treatment and turning it into slag, the basicity of the slag is lowered and its fluidity is improved.

これが本発明の第1の要点である。This is the first point of the invention.

この場合、脱Siスラグに−J粒度が小さく且つ均一な
ものが好ましく、これを得るためには、吸引式スラグ、
クリーナーで脱Siスラグを吸引後水冷すればよい。
In this case, it is preferable that the -J particle size is small and uniform for the Si-removed slag, and in order to obtain this, suction type slag,
It is sufficient to suck the Si-removed slag with a cleaner and then cool it with water.

本発明の第2の要点は、脱Siスラグの添加、滓化時期
である。
The second point of the present invention is the addition of Si-free slag and the timing of slag formation.

既に述べた如く、脱P処理又は脱S、脱P同時処理にお
いて、処理スラグ中の塩基度は脱P効率を高めるために
ある程度高い方がよい。
As already mentioned, in the deP treatment or simultaneous de-S and de-P treatment, the basicity in the treated slag is preferably high to some extent in order to improve the efficiency of de-P.

しかるに処理スラグの流動性を高めるべく、処理の初期
〜中期に脱Siスラグを添加すると、処理中に処理スラ
グの塩基度が低下し、脱P効率が低下する。
However, if a Si-removal slag is added in the early to middle stages of treatment in order to increase the fluidity of the treated slag, the basicity of the treatment slag decreases during the treatment, resulting in a decrease in P removal efficiency.

そこで本発明ではこの様な不都合を回避すべく、欠配す
る時期に脱Siスラグを添加するものである。
Therefore, in the present invention, in order to avoid such inconvenience, the Si-free slag is added at the time of shortage.

即ち、1脱P処理、同時脱S、脱P処理終了後添加し滓
化する。
That is, it is added after one P-removal treatment, simultaneous S-removal, and P-removal treatment to form a slag.

2脱P処理の末期、同時脱S、脱P処理の末期に添加し
滓化する。
2. It is added at the end of the P removal process, simultaneous deS, and the end of the P removal process to form a slag.

3脱P処理の末期、同時脱S、脱P処理の末期から同処
理終了後にかげて添加し滓化する。
3. It is added at the end of the P-removal process, simultaneous S-removal, and from the end of the P-removal process to after the end of the process to form a slag.

上記2,3の場合の処理末期とは、処理終了時点から3
〜5分以降が好ましい。
In cases 2 and 3 above, the end of processing is 3 years from the end of processing.
~5 minutes or more is preferred.

この様に脱P処理、同時脱S、脱P処理がはg又は完全
に終了後に脱Siスラグを添加し滓化することにより、
処理スラグの塩基度低下による処理効率低下の懸念はな
(・。
In this way, by adding Si-free slag and turning it into slag after the P-removal treatment, simultaneous S-removal, and P-removal treatment are completed or completed,
There is no concern that the processing efficiency will decrease due to a decrease in the basicity of the treated slag (・.

以下実施例を説明する。Examples will be described below.

実施例 1(脱P処理) Si0.55係、so、ois饅、Po、115優、温
度1340℃の溶銑を処理容器に100 ton収容し
、鉄鉱石を投入し、ガス攪拌を行なうと共に酸素を上吹
きして15分間処理してSiO,15φ、80.018
俤、Po、115係の溶銑を得た。
Example 1 (P removal treatment) 100 tons of hot metal with Si 0.55, SO, OIS, Po 115, and a temperature of 1340°C was placed in a processing vessel, iron ore was charged, gas was stirred, and oxygen was removed. Top-blown and processed for 15 minutes to form SiO, 15φ, 80.018
Po, No. 115 hot metal was obtained.

この脱Si処理後生成スラグを久保田鉄工製のスラグ。The slag produced after this Si removal process is manufactured by Kubota Iron Works.

クリーナーにより、上部から吸引排出しなから水滓化し
た。
The cleaner sucked it out from the top and turned it into a water slag.

得られた脱SiスラグのSiO2含有量は45ダであり
、又粒度は2a以下であった。
The SiO2 content of the obtained Si-free slag was 45 da, and the particle size was 2a or less.

脱Si処理排滓後溶銑を移しかえることなく、CaO系
フラックスを添加すると共にインペラー攪拌を行なL・
、更に酸化鉄投入、酸素上吹きにより15分間脱P処理
し、処理終了後、上記脱Siスラグ水滓を300@添加
して滓化したところ、スラグの塩基度は2.2であった
After the Si removal treatment, without transferring the hot metal, CaO-based flux is added and impeller stirring is performed.
Further, the slag was dephosphorized by adding iron oxide and top-blowing oxygen for 15 minutes, and after the treatment was completed, 300 @ of the above-described desiliconized slag water slag was added to form a slag, and the basicity of the slag was 2.2.

しかるのちこのスラグをスラグ、クリーナーにより吸引
排出した。
Afterwards, this slag was suctioned out using a slag cleaner.

尚、得られた溶銑のSiは0.01%、Sは0.017
俤、Pは0.015%であった。
In addition, the Si content of the obtained hot metal was 0.01%, and the S content was 0.017%.
P was 0.015%.

第1図に本実施例における脱Siスラグの吸引排出効率
と、上記実施例にお℃゛て脱Siスラグを添加しない場
合の脱Pスラグの吸引排出効率を示した。
FIG. 1 shows the suction and discharge efficiency of the Si-free slag in this example, and the suction and discharge efficiency of the P-free slag in the case where the Si-free slag is not added to the above example.

これから明らかな如く、本発明実施例によれば、短時間
にスラグの排出が終了したことが判る。
As is clear from this, according to the embodiment of the present invention, the discharge of slag was completed in a short time.

これに対して、脱Siスラグを添加しなL・従来法では
、表面温度の低下に伴ない硬化が進んで、50φ位しか
除滓できなかった。
On the other hand, in the L/conventional method without adding Si-removal slag, hardening progressed as the surface temperature decreased, and only about 50 mm of slag could be removed.

実施例 2(同時脱S、脱P) 実施例1と同様な方法で脱Si処理し、排滓後溶銑を移
しかえることなく、CaO−CaCl2系フラックスを
添加すると共に、インペラー攪拌、酸化鉄投入、及び酸
素上吹きにより20分分間時脱S、脱P処理した。
Example 2 (simultaneous de-S, de-P) De-Si treatment was performed in the same manner as in Example 1, and without transferring the hot metal after slag, CaO-CaCl2-based flux was added, stirring was carried out using an impeller, and iron oxide was added. , and oxygen top-blowing for 20 minutes to remove S and P.

処理終了3分前に上記脱Siスラグ水滓を500に7添
加し滓化したところ、処理終了時点でスラグの塩基度は
2.5であった。
Three minutes before the end of the treatment, the above-mentioned Si-removed slag water slag was added to 500:7 to form a slag, and the basicity of the slag was 2.5 at the end of the treatment.

しかるのちこのスラグをスラグ、クリーナーにより吸引
排出した。
Afterwards, this slag was suctioned out using a slag cleaner.

尚、得られた溶銑成分は、Si0.01%、SO,00
9%、Po、012%で所期の値が得られた。
In addition, the obtained hot metal components were Si0.01%, SO,00
The expected values were obtained at 9% and Po, 012%.

本実施例における同時脱S、脱Pスラグの吸引排出効率
と、上記実施例におし゛て脱Siスラグを添加しなL・
場合の同時脱S、脱Pスラグの吸引排出効率を第2図に
示す。
Simultaneous S removal in this example, suction and discharge efficiency of deP slag, and L-removal without adding deSi slag in the above example.
Figure 2 shows the simultaneous de-S and suction and discharge efficiency of de-P slag.

これより明らかな如く本実施例によれば、短時間にスラ
グの排出が終了したことが判る。
As is clear from this, according to this example, the slag discharge was completed in a short time.

これに対して脱Siスラグを添加しない従来法では30
%位しか除滓できなかった。
On the other hand, in the conventional method without adding Si-removal slag, 30
Only about % could be removed.

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

第1図及び第2図は、本発明方法による場合と本発明に
よらない場合のスラグの吸引排出効率を示す図表である
FIG. 1 and FIG. 2 are charts showing the slag suction and discharge efficiency when using the method of the present invention and when not using the method of the present invention.

Claims (1)

【特許請求の範囲】[Claims] 1 溶銑を脱Si処理後排滓し、引続いて脱P処理又は
同時脱S、脱P処理後排滓する溶銑の分割精錬において
、上記脱P処理又は同時脱S、脱P処理の末期成いは処
理終了後若しくは処理末期から処理終了後にかげて上記
脱Si処理排滓スラグを添加して滓化し、上記脱P又は
同時脱S、脱P生成スラグの流動性を高めてのち、同生
成スラグを吸引排出することを特徴とする溶銑スラグの
吸引除去方法。
1 In split refining of hot metal in which hot metal is slaged after Si-removal treatment, followed by de-P treatment or simultaneous de-S, and slag after de-P treatment, the above-mentioned de-P treatment, simultaneous de-S, or final formation of the de-P treatment is performed. Alternatively, after the completion of the treatment, or from the end of the treatment to the end of the treatment, the above-mentioned Si-removed slag is added and turned into slag, and the fluidity of the above-mentioned deP or simultaneous de-S or de-P generated slag is increased, and then the same process is performed. A method for suctioning and removing hot metal slag, characterized by sucking and discharging the slag.
JP3764281A 1981-03-16 1981-03-16 Method for suction removal of hot metal processing slag Expired JPS5838483B2 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP3764281A JPS5838483B2 (en) 1981-03-16 1981-03-16 Method for suction removal of hot metal processing slag
AU81512/82A AU527082B2 (en) 1981-03-16 1982-03-15 Removing slag by suction after increasing fluidity
BR8201399A BR8201399A (en) 1981-03-16 1982-03-15 PROCESS OF REMOVING DRAIN FROM THE METAL SURFACE IN SUCCESS FUSION
EP82301304A EP0060706A1 (en) 1981-03-16 1982-03-15 Method for removing slag on the surface of molten metal by suction

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3764281A JPS5838483B2 (en) 1981-03-16 1981-03-16 Method for suction removal of hot metal processing slag

Publications (2)

Publication Number Publication Date
JPS57152406A JPS57152406A (en) 1982-09-20
JPS5838483B2 true JPS5838483B2 (en) 1983-08-23

Family

ID=12503300

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3764281A Expired JPS5838483B2 (en) 1981-03-16 1981-03-16 Method for suction removal of hot metal processing slag

Country Status (1)

Country Link
JP (1) JPS5838483B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101485529B1 (en) 2013-08-07 2015-01-22 주식회사 포스코 Refining method of molten steel and an apparatus thereof

Also Published As

Publication number Publication date
JPS57152406A (en) 1982-09-20

Similar Documents

Publication Publication Date Title
JPS5514802A (en) Treating method for molten metal generated at reduction treatment for slag from steel manufacture
JPH11158526A (en) Method for producing high P slag
JPS5838483B2 (en) Method for suction removal of hot metal processing slag
JP2653301B2 (en) Reusing method of low P converter slag
JP4369632B2 (en) Pretreatment method of hot metal with low slag generation using converter type vessel
JP3772918B2 (en) Dephosphorization method of hot metal in converter type refining vessel
JP2833736B2 (en) Hot metal pretreatment method
JP3747880B2 (en) Hot metal pretreatment method
JP2880842B2 (en) How to make clean steel
JPS5838484B2 (en) How to suction molten metal processing slag
JPS5831012A (en) Preferential desiliconizing method for molten iron by blowing of gaseous oxygen
JP3898964B2 (en) Dephosphorization method for hot metal
JPH0892618A (en) Prerefining method
JP4224910B2 (en) Hot treatment method for molten slag produced during hot metal decarburization treatment
JPH1150122A (en) Dephosphorization refining method of hot metal in converter type refining vessel
JPS6154081B2 (en)
JPS58181815A (en) Preliminary desiliconization method for hot metal using a converter
JPH05320731A (en) Effective use of AOD furnace dust collection
JPS5852529B2 (en) Method for dephosphorizing hot metal
JPS6140005B2 (en)
JPS5819421A (en) Manufacture of steel with converter
JP2002069518A (en) Dephosphorization of hot metal with low slag generation
JP2000073113A (en) Desiliconization of molten iron
JPS5855504A (en) Manufacture for pig and steel
JP2004339552A (en) Hot metal dephosphorization method