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JPS6154843B2 - - Google Patents
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JPS6154843B2 - - Google Patents

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Publication number
JPS6154843B2
JPS6154843B2 JP2193480A JP2193480A JPS6154843B2 JP S6154843 B2 JPS6154843 B2 JP S6154843B2 JP 2193480 A JP2193480 A JP 2193480A JP 2193480 A JP2193480 A JP 2193480A JP S6154843 B2 JPS6154843 B2 JP S6154843B2
Authority
JP
Japan
Prior art keywords
blowing
steel
carbon content
oxygen
amount
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
JP2193480A
Other languages
Japanese (ja)
Other versions
JPS56123314A (en
Inventor
Takeshi Takanawa
Yoshisuke Yoshisaka
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 JP2193480A priority Critical patent/JPS56123314A/en
Publication of JPS56123314A publication Critical patent/JPS56123314A/en
Publication of JPS6154843B2 publication Critical patent/JPS6154843B2/ja
Granted 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
    • C21C5/00Manufacture of carbon-steel, e.g. plain mild steel, medium carbon steel or cast steel or stainless steel
    • C21C5/28Manufacture of steel in the converter
    • C21C5/42Constructional features of converters
    • C21C5/46Details or accessories
    • C21C5/4673Measuring and sampling devices

Landscapes

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)

Description

【発明の詳細な説明】 本発明は転炉操業における鋼中炭素含有量のダ
イナミツク終点制御方法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for dynamic endpoint control of carbon content in steel in converter operation.

転炉吹錬においては吹止時の溶鋼の温度、成
分、特に炭素含有量を目標値に適中させるのが最
重要課題である。従つて吹錬途中にて転炉の排ガ
スの分析若しくは流量計測、又はサブランスによ
る溶鋼温度、鋼中炭素含有量の計測等を行つて、
計測時点の鋼中炭素含有量を求め、爾後の操業条
件を修正する所謂ダイナミツク終点制御が開発さ
れて適中率の向上が図られている。このダイナミ
ツク終点制御方法においては、脱炭速度又は前記
計測時点から終点までに吹込むべき酸素量と、鋼
中炭素含有量とを対応づけるモデルの良否、即ち
計測値により終点炭素含有量を精度良く推定し得
るか否か、またモデルの表現方法が簡潔であり、
このモデルにより制御し得る適用範囲が広いか否
かが、その実用性を評価する上で重要である。と
ころでこのモデルとして、脱炭速度を鋼中炭素含
有量について指数関数表示するものが提案されて
いるが、モデルを同定すること、即ち指数関数に
おける係数を実操業データから多重回帰分析によ
つて、あらゆる操業状態に対応できるように決定
するのは容易ではない。また特開昭52−5613にお
いては、吹錬末期における実測鋼中炭素量と、こ
の計測時点から終点までの吹込酸素量と、終点炭
素含有量との関係を実操業データから炉別、鋼種
別、更には吹錬末期における実測鋼中炭素量が同
一水準にあるもの毎に抽出群別し、各群毎に該計
測時点から終点までの脱炭曲線(即ち吹込酸素量
と終点炭素含有量との関係)を作成しておき、制
御しようとする吹錬操業において、吹錬末期に鋼
中炭素量を計測して上記種々の脱炭曲線から適合
するものを選択し、目標終点炭素含有量から終点
までに吹込むべき酸素量を決定する方法を提案し
ている。しかしながら、このような方法ではこれ
ら種々の操業条件及び実測鋼中炭素量毎に脱炭曲
線を作成するため、モデルの同定作業が極めて繁
雑であり実用的でない。
In converter blowing, the most important issue is to adjust the temperature and composition of molten steel, especially the carbon content, to target values at the time of blow-off. Therefore, during the blowing process, analyze the exhaust gas from the converter or measure the flow rate, or measure the molten steel temperature and carbon content in the steel using a sublance.
A so-called dynamic end-point control has been developed that determines the carbon content in steel at the time of measurement and adjusts subsequent operating conditions to improve accuracy. In this dynamic end point control method, the end point carbon content can be accurately determined based on the quality of the model that correlates the decarburization rate or the amount of oxygen to be blown from the measurement point to the end point with the carbon content in the steel. whether it can be estimated or not, and the method of expressing the model is concise;
Whether or not the range of application that can be controlled by this model is wide is important in evaluating its practicality. By the way, a model has been proposed in which the decarburization rate is expressed as an exponential function with respect to the carbon content in steel, but it is necessary to identify the model, that is, to calculate the coefficients in the exponential function from actual operation data by multiple regression analysis. It is not easy to make a decision that can accommodate all operating conditions. In addition, in JP-A-52-5613, the relationship between the actually measured carbon content in steel at the final stage of blowing, the amount of oxygen blown from this measurement point to the end point, and the end point carbon content was determined by furnace and steel type based on actual operation data. In addition, the samples are divided into extraction groups according to the fact that the measured carbon content in the steel at the end of blowing is at the same level. In the blowing operation that is to be controlled, the carbon content in the steel is measured at the end of the blowing process, a suitable decarburization curve is selected from the various decarburization curves mentioned above, and the carbon content is calculated from the target end point carbon content. A method is proposed to determine the amount of oxygen that should be injected until the end point. However, in such a method, a decarburization curve is created for each of these various operating conditions and measured carbon content in steel, so the model identification work is extremely complicated and is not practical.

本発明は斯かる事情に鑑みてなされたものであ
つて、脱炭速度又は吹錬末期における鋼中炭素含
有量計測時点から終点までに吹込むべき酸素量
と、前記実測鋼中炭素含有量とを簡潔に且つ精度
良く対応づける数式を提案し、該数式に基いて終
点炭素含有量を制御する方法を提供することを目
的とする。
The present invention has been made in view of such circumstances, and it is possible to determine the amount of oxygen to be blown from the time of measuring the decarburization rate or the carbon content in steel at the end of blowing to the end point, and the actual carbon content in steel. The purpose of the present invention is to propose a mathematical formula that correlates the two concisely and accurately, and to provide a method for controlling the end point carbon content based on the mathematical formula.

本発明に係る鋼中の炭素含有量制御方法は、転
炉操業における吹錬末期の酸素消費速度を鋼中の
炭素含有量の多項式で表わすこととし、該多項式
並びに吹錬終点前の適宜時点にてサブランス計測
によつて得た鋼中の炭素含有量CS、前記時点か
ら吹錬終点に至る間の吹込酸素量ΔO2及び吹錬
終点における鋼中の炭素含有量CEを少くとも含
む実績データに基き、これらの変数の相関関係を
表わす後述の(7)式を得ておき吹錬の都度、吹錬終
点前の適宜時点にてサブランス計測によつて得た
鋼中の炭素含有量をCS、吹錬終点における鋼中
の目標炭素含有量をCEとして、少くともこれら
を(7)式に与えることにより、上記時点から吹錬終
点に至る間の所要吹込酸素量をΔO2として算出
し、この算出結果に基いて転炉操業を行うことを
特徴とする。
In the method for controlling carbon content in steel according to the present invention, the oxygen consumption rate at the final stage of blowing in converter operation is expressed by a polynomial of the carbon content in steel, and the polynomial and the appropriate time before the end of blowing are A track record that includes at least the carbon content C S in the steel obtained by sublance measurement at Based on the data, we obtained equation (7) below, which expresses the correlation between these variables, and calculated the carbon content in the steel by sublance measurement at an appropriate point before the end of each blowing process. C S , the target carbon content in the steel at the end point of blowing is C E , and by giving at least these to equation (7), the required amount of blown oxygen from the above point to the end point of blowing is ΔO 2 The method is characterized in that the converter is operated based on the calculation result.

以下本発明方法について詳述する。酸素吹錬過
程を数式表現するために、脱炭速度VCを下記(1)
式の如く表わすこととすると、脱炭速度VCと鋼
中炭素含有量Cとの間には第1図に示す如き指数
関数で表わされるべき関係が存在する。
The method of the present invention will be explained in detail below. In order to express the oxygen blowing process mathematically, the decarburization rate V C is expressed as below (1)
If expressed as in the equation, there exists a relationship between the decarburization rate V C and the carbon content C in steel that should be expressed as an exponential function as shown in FIG.

C=dC/d(O/WST) ……(1) 但し、C:鋼中の炭素含有量(%) O2:酸素量(Nm3) WST:主原料装入量から推定した溶鋼重量
(T) 即ちVCはCが零のときは零であり、Cの増大
とともに大きくなるが、このVCの増加はある程
度Cが増大すると飽和鈍化する。ところで酸素消
費速度VOを下記(2)式の如くVCの逆数として定義
すると、VOとCとの関係は第2図の如き双曲線
関係で表わされるべきものとなる。
V C = dC/d(O 2 /W ST ) ...(1) However, C: Carbon content in steel (%) O 2 : Oxygen amount (Nm 3 ) W ST : Estimated from the amount of main raw material charged The molten steel weight (T), that is, V C is zero when C is zero, and increases as C increases, but this increase in V C becomes saturated and slows down when C increases to a certain extent. By the way, if the oxygen consumption rate V O is defined as the reciprocal of V C as shown in equation (2) below, the relationship between V O and C should be expressed as a hyperbolic relationship as shown in FIG.

O=d(O/WST)/dC ……(2) このVOとCとの関係は、Cが零に近づくとVO
は極めて大きくなり、Cが零のときは見掛上VO
は∞となる。またCが大きくなるとVOの低下は
飽和鈍化し、Cが極めて大きくなるとVOはある
一定値に近づく。これらを数式表現すると 但し、a0:定数 となり、酸素消費速度VOと鋼中炭素含有量Cと
の関係を表わす数式は(3)、(4)式の条件を満足する
必要がある。
V O = d(O 2 /W ST )/dC ...(2) The relationship between V O and C is that when C approaches zero, V O
becomes extremely large, and when C is zero, the apparent V O
becomes ∞. Further, as C becomes larger, the decrease in V O becomes saturated and slower, and when C becomes extremely large, V O approaches a certain constant value. Expressing these mathematically However, a 0 is a constant, and the formula expressing the relationship between the oxygen consumption rate V O and the carbon content C in the steel must satisfy the conditions of formulas (3) and (4).

本願発明者等はこのような酸素吹錬過程を適切
に表現するモデル数式を得るために、多数の実操
業データを使用して種々検討した結果、下記(5)式
が鋼中炭素含有量の計測値から終点炭素含有量を
推定する際の精度を確保する上で適当との結論を
得た。
In order to obtain a model formula that appropriately expresses the oxygen blowing process, the inventors of the present application conducted various studies using a large amount of actual operation data, and as a result, the following formula (5) was found to represent the carbon content in steel. It was concluded that this method is appropriate for ensuring accuracy when estimating end point carbon content from measured values.

d(O/WST)/dC=a0+a/C+a/C
+a/C……(5) 但し、a1〜a3:定数 なおこの(5)式は前記(3),(4)式を満足することは
勿論である。また(5)式右辺の項を炭素含有量Cの
−3乗項までとしたのは、Cの−4乗項以上を採
用した場合にも精度向上面での実質的効果が得ら
れなかつたためである。即ち、酸素消費速度VO
と鋼中炭素含有量Cとの間に第2図に示した曲線
の如き関係が存在するためには、(5)式のCの係数
a0,a1,a2,a3、更にはこねに続くべき−4乗項
のa4,−5乗項のa5…は全て同符号であることを
要するが、多項式の次数を増した場合に、実操業
データを使用し多重回帰分析を行つてCの係数
a0,a1,a2,a3,a4,a5…を得ても、これら全て
の係数が同符号になることは不可能に近く、その
ような数式を酸素吹錬過程を表現する式として採
用することは、物理的意義に欠けることになるか
らである。
d( O2 / WST )/dC= a0 + a1 /C+ a2 / C2
+a 3 /C 3 ...(5) However, a 1 to a 3 are constants. It goes without saying that this equation (5) satisfies the above equations (3) and (4). In addition, the reason why the term on the right side of equation (5) is limited to the -3rd power term of the carbon content C is that even if the -4th power term or higher of C is adopted, no substantial effect in terms of accuracy improvement can be obtained. It is. That is, the oxygen consumption rate V O
In order for a relationship like the curve shown in Figure 2 to exist between C and the carbon content in steel, the coefficient of C in equation (5) must be
a 0 , a 1 , a 2 , a 3 , and furthermore, a 4 of the −4th power term and a 5 of the −5th power term following the kneading must all have the same sign, but it is necessary to increase the degree of the polynomial. In this case, perform multiple regression analysis using actual operation data to calculate the coefficient of C.
Even if we obtain a 0 , a 1 , a 2 , a 3 , a 4 , a 5 , etc., it is almost impossible for all these coefficients to have the same sign, and such a formula cannot be used to express the oxygen blowing process. This is because adopting it as a formula would lack physical significance.

さて吹錬末期のサブランスによる鋼中の炭素含
有量計測時点から吹錬終点に至る期間の酸素吹錬
過程に前記(5)式を適用すると、下記(6)式の如く該
期間における吹込酸素量を得ることができる。
Now, if we apply the above equation (5) to the oxygen blowing process from the time when the carbon content in the steel is measured by the sub-lance at the end of blowing to the end of blowing, the amount of blown oxygen during that period as shown in equation (6) below. can be obtained.

ΔO/WST=∫CS CEd(O/WST)/dC・dC=a0(CS−CE)+a1 o(C/C) +a2〔(−1/C)−(−1/C)〕+a3〔1/2(−1/C )−1/2(−1/C )〕……(6
) 但し、ΔO2:サブランス計測時点から吹錬終
点までに吹込まれた酸素量(N
m3) CS:吹錬末期のサブランス計測による鋼
中炭素含有量計測値(%) CE:吹錬終点における鋼中炭素含有量
(%) 従つて多数の実操業データに基き、ΔO2,CS
及びCEを(6)式に代入し、多重回帰分析によつて
(6)式の各定数a0〜a3を決定すれば、制御しようと
する吹錬においては、吹錬末期に鋼中炭素含有量
をサブランスによつて計測してこれをCSとし、
目標終点炭素含有量をCEとして、(6)式に代入し
サブランス計測時点から吹錬終点までに吹込むべ
き酸素量ΔO2を算出することにより終点炭素含
有量を制御できる。
ΔO 2 /W ST =∫ CS CE d(O 2 /W ST )/dC・dC=a 0 (C S −C E )+a 1 o (C S /C E ) +a 2 [(-1/C S )−(−1/C E )]+a 3 [1/2(−1/C S 2 )−1/2(−1/C E 2 )]……(6
) However, ΔO 2 : The amount of oxygen (N
m 3 ) C S : Measured value of carbon content in steel by sublance measurement at the end of blowing (%) C E : Carbon content in steel at the end of blowing (%) Therefore, based on a large amount of actual operation data, ΔO 2 , C S
and C E into equation (6), and by multiple regression analysis,
Once each constant a 0 to a 3 in equation (6) is determined, in the blowing to be controlled, the carbon content in the steel is measured with a sublance at the end of the blowing, and this is set as C S .
The end point carbon content can be controlled by setting the target end point carbon content as C E and substituting it into equation (6) to calculate the amount of oxygen ΔO 2 to be blown from the time of sublance measurement to the end point of blowing.

然るところ、溶鋼温度及び鋼浴中に投入された
副原料の量も、サブランス計測後の脱炭反応の進
行に影響を与えるので、制御精度をより向上させ
るために、ΔO2を求める数式は(6)式にKを加え
た下記(7)式を採用するのが実用的である。
However, since the molten steel temperature and the amount of auxiliary materials introduced into the steel bath also affect the progress of the decarburization reaction after sublance measurement, the formula for calculating ΔO 2 is It is practical to adopt the following equation (7), which is obtained by adding K to equation (6).

ΔO/WST=a0(CS−CE)+a1 o(C/C)+a2〔(−1/C)−(−1/C)〕 +a3〔1/2(−1/C )−1/2(−1/C )〕+K ……(7) ここでKは制御対象とする転炉操業の条件にて
定まる変数であつて、下記(8)式から得られる。
ΔO 2 /W ST = a 0 ( CSCE ) + a 1 o ( CS / CE ) + a 2 [(-1/ CS ) −(-1/ CE )] + a 3 [1/2 (-1/C S 2 )-1/2 (-1/C E 2 )]+K...(7) Here, K is a variable determined by the conditions of converter operation to be controlled, and is expressed as follows ( 8) can be obtained from Eq.

K=T(TSS)+HT(WHT/WST−W
/WST) +CA(WCA/WST−WCA/WST)+L…
…(8) 但し、TS:吹錬未期のサブランス計測による
溶鋼温度計測値(℃) S:吹錬末期のサブランス計測時点にお
ける溶鋼温度基準値(℃) WHT:吹錬開始後サブランス計測時点まで
の期間中に投入された蛍石量
(T) HT:吹錬開始後サブランス計測時点まで
の期間中に投入されるべき蛍石量
の基準値(T) WCA:吹錬開始後サブランス計測時点まで
の期間中に投入された石灰石量
(T) CA:吹錬開始後サブランス計測時点まで
の期間中に投入されるべき石灰石
量の基準値(T) ST:溶鋼重量基準値(T) THTCA:定数 L :制御対象吹錬に先行する複数のチ
ヤージ(例えば10数チヤージ)の
制御実績から決定される時系列的
変動補正項であつて、例えば炉の
使用回数を重ねることによつて、
炉内耐火物が損傷し、炉内容量の
若干の変動によつて鋼浴表面と送
酸ランス間の離隔距離が若干変動
するなどのために生ずる誤差を補
正するための項 この(7),(8)式に前述したのと同様に実操業デー
タを使用して多重回帰分析を行い、各定数a0
a3THTCAを決定する。なお溶鋼温度
補正項T(TSS)の係数Tは、高温程脱炭
効率が高いために負となるべきものである。
K= T (T S - S ) + HT (W HT /W ST - W H
T
/W ST ) + CA (W CA /W ST - W CA /W ST ) + L...
…(8) However, T S : Measured value of molten steel temperature by sublance measurement before blowing (°C) S : Reference value of molten steel temperature at the time of sublance measurement at the end of blowing (°C) W HT : Sublance measurement after blowing starts Amount of fluorite that has been added during the period up to the point in time (T) HT : Standard value for the amount of fluorite that should be added during the period from the start of blowing to the time of sublance measurement (T) W CA : Sublance after the start of blowing Amount of limestone that should be added during the period up to the measurement point (T) CA : Standard value for the amount of limestone that should be added during the period from the start of blowing to the time of sublance measurement (T) ST : Standard value for the weight of molten steel (T) T , HT , CA : Constant L: Time-series fluctuation correction term determined from the control performance of multiple charges (for example, 10-odd charges) preceding the controlled object blowing, for example, by increasing the number of times the furnace is used According to
This section (7) is for correcting errors that occur due to damage to the refractories in the furnace and slight fluctuations in the distance between the steel bath surface and the oxygen supply lance due to slight fluctuations in the volume inside the furnace. Multiple regression analysis was performed using actual operation data in the same way as described above for formula (8), and each constant a 0 ~
Determine a 3 , T , HT , and CA. Note that the coefficient T of the molten steel temperature correction term T ( TSS ) should be negative because the higher the temperature, the higher the decarburization efficiency.

また基準値HTCA及びSTは多数の実操業
データを使用して多重回帰分析を行う時に、その
実操業データの平均値として求める。また補正項
Lは以下の様にして求める。即ち、毎チヤージの
吹錬後にL=0として(7)式の右辺に実績データを
代入することによつてΔO2/WSTの推定値を算
出し、これとΔO2/WSTの実績値との差をΔ
O2/WSTの推定誤差量とする。そして複数の先
行チヤージにおけるΔO2/WSTの推定誤差量の
平均値をLとする。
In addition, the reference values HT , CA , and ST are obtained as the average value of the actual operation data when performing multiple regression analysis using a large number of actual operation data. Further, the correction term L is determined as follows. That is, after each charge blowing, the estimated value of ΔO 2 /W ST is calculated by setting L = 0 and substituting the actual data on the right side of equation (7), and this and the actual value of ΔO 2 /W ST are calculated. The difference between
Let O 2 /W be the estimated error amount of ST . Then, let L be the average value of the estimated error amount of ΔO 2 /W ST in a plurality of preceding charges.

而して本発明は上記(7),(8)式に基き、目標炭素
含有量を有する溶鋼を得るために、サブランス計
測時点から吹錬終点に至る間に吹込むべき酸素量
ΔO2を推定し、これによつて終点炭素含有量を
制御するものであるが、(7),(8)式によつた場合に
おいてこのモデル数式の妥当性及び多重回帰分析
により求められた各係数a0〜a3T等の妥当性
を酸素量ΔO2の推定精度として第3図に示す。
即ち第3図は横軸に酸素量の推定値を、縦軸に実
績値を、夫々単位溶鋼重量あたりでとつて表わ
し、推定値と実績値とが等しい状態を実線による
直線で、またこの直線の±1Nm3/Tの値を破線
で示している。ここに実績値とはサブランス計測
時点から吹錬終点までの期間に実際に吹込まれた
酸素量であつて、推定値というのはこの吹錬によ
つて得られた溶鋼の終点炭素含有量CEとサブラ
ンス計測によつて求められた計測値CS,TS
(7),(8)式に代入して算出された酸素量ΔO2であ
る。要するに終点炭素含有量CEの溶鋼を得るた
めに、サブランス計測時点から吹錬終点までに吹
込むべき酸素量を、(7),(8)から求めた推定値と、
実際に吹込まれた実績値とによつて比較して、
(7),(8)式の推定精度を検討した。図から明らかな
如く推定精度は極めて高く、±1Nm3/Tの範囲内
に86チヤージ中77チヤージが含まれ、±1Nm3/T
の範囲で90%という高率の推定精度が得られた。
Based on the above equations (7) and (8), the present invention estimates the amount of oxygen ΔO 2 that should be blown between the time of sublance measurement and the end of blowing in order to obtain molten steel with the target carbon content. This controls the carbon content at the end point, but in the case of formulas (7) and (8), the validity of this model formula and each coefficient a 0 ~ Figure 3 shows the validity of a 3 , T , etc. as the estimation accuracy of oxygen amount ΔO 2 .
In other words, in Figure 3, the horizontal axis represents the estimated value of oxygen content, and the vertical axis represents the actual value, each measured per unit weight of molten steel. The value of ±1Nm 3 /T is shown by the broken line. Here, the actual value is the amount of oxygen actually blown in from the time of sublance measurement to the end point of blowing, and the estimated value is the end point carbon content C E of the molten steel obtained by this blowing. and the measured values C S and T S obtained by sublance measurement.
This is the oxygen amount ΔO 2 calculated by substituting into equations (7) and (8). In short, in order to obtain molten steel with the end point carbon content CE , the amount of oxygen that should be blown from the time of sublance measurement to the end point of blowing is estimated from (7) and (8),
Compared with the actual value actually injected,
We examined the estimation accuracy of equations (7) and (8). As is clear from the figure , the estimation accuracy is extremely high, with 77 out of 86 charges falling within the range of ±1Nm 3 /T.
A high estimation accuracy of 90% was obtained in the range of .

さて本発明方法は前記(7),(8)式を予め用意して
おいた上で次のようにして行われる。即ち、従来
の操業経験から又はスタテイツク終点制御方法に
よつて、目標成分及び温度の溶鋼を得るための、
主原料及び副原料装入量並びに送酸パターン及び
吹錬時間等の吹錬条件等を決定する。而してこの
ように決定された操業条件により吹錬を開始した
後、吹錬終点前の適宜時点にて、サブランス計測
によつて鋼中の炭素含有量CS及び溶鋼温度TS
計測する。なお上記適宜時点とは2分前程度であ
るが、送酸速度などにより適宜変更することがで
きる。けだしサブランス計測時点から予測吹錬終
点までの時間が長きに過ぎると制御が困難になり
適中精度が低下し、また短きに過ぎると鋼中炭素
含有量が既に目標値以下に低下し、終点炭素含有
量の制御が不能になる事態が想定されるからであ
る。なお前述の(7),(8)式を同定するための鋼中炭
素含有量等を得るために行うサブランス計測も、
吹錬終点前の適宜時点に行うことは勿論である。
Now, the method of the present invention is carried out as follows after preparing the above-mentioned equations (7) and (8) in advance. That is, to obtain molten steel with a target composition and temperature based on conventional operational experience or by a static end point control method,
Determine the amount of main raw materials and auxiliary raw materials to be charged, as well as blowing conditions such as oxygen supply pattern and blowing time. After starting blowing under the operating conditions determined in this way, the carbon content C in the steel and the molten steel temperature T are measured by sublance measurement at an appropriate time before the end of blowing. . Note that the above-mentioned appropriate time point is about 2 minutes ago, but it can be changed as appropriate depending on the oxygen delivery rate and the like. If the time from the time of sublance measurement to the predicted end point of blowing is too long, control will become difficult and accuracy will decrease; if it is too short, the carbon content in the steel has already fallen below the target value, and the end point carbon This is because it is assumed that the content may become uncontrollable. Furthermore, the sublance measurement performed to obtain the carbon content in steel to identify the above-mentioned equations (7) and (8) is also
Of course, this can be done at an appropriate time before the end of blowing.

而して前記吹錬終点前の適宜時点にて、サブラ
ンス計測された鋼中炭素含有量CS及び溶鋼温度
Sを、終点炭素含有量の目標値CEとともに、
(7),(8)式に代入し、上記サブランス計測時点から
吹錬終点に至る間の所要吹込酸素量ΔO2を算出
する。この算出においてWSTは下記(9)式かららW
HM等の各主原料装入量に基き算出する。
Then, at an appropriate time before the end point of the blowing, the carbon content in the steel C S and the molten steel temperature T S measured by the sublance, together with the target value C E of the end point carbon content,
By substituting into equations (7) and (8), the required amount of blown oxygen ΔO 2 from the time of sublance measurement to the end point of blowing is calculated. In this calculation, W ST is calculated from Equation (9) below.
Calculated based on the charging amount of each main raw material such as HM .

ST=α(WHM+WCM)+βWSCR +γWORE+δWSCA ……(9) 但し、WHM:溶銑重量(T) WCM:冷銑重量(T) WSCR:スクラツプ重量(T) WORE:鉄鉱石重量(T) WSCA:スケール重量(T) α、β、γ、δ:定数 定数α,β,γ及びδは夫々銑鉄、スクラツ
プ、鉄鉱石及びスケールの溶鋼への歩留りであり
(9)式に多重回帰分析を適用して求める。
W ST = α (W HM + W CM ) + βW SCR + γW ORE + δW SCA ...(9) However, W HM : Hot metal weight (T) W CM : Cold pig iron weight (T) W SCR : Scrap weight (T) W ORE : Iron ore weight (T) W SCA : Scale weight (T) α, β, γ, δ: Constants Constants α, β, γ, and δ are the yield of pig iron, scrap, iron ore, and scale into molten steel, respectively.
It is obtained by applying multiple regression analysis to equation (9).

なお、スケール等の装入量は基本的には吹錬開
始時に装入される量であるが、溶鋼温度調節等の
ために吹錬中にサブランス計測時点までに投入さ
れた場合は、これを加算してWSTを算出するのが
好ましい。WHT,WCAについても同様である。
The amount of scale etc. to be charged is basically the amount charged at the start of blowing, but if it is added before sublance measurement during blowing to adjust the molten steel temperature, etc. It is preferable to calculate W ST by adding. The same applies to W HT and W CA.

このようにしてサブランス計測後の所要吹込酸
素量ΔO2が求まると、このΔO2の量の酸素を吹
き終えた時点で送酸を停止することにより、終点
炭素含有量はその目標値CEに一致することにな
る。
Once the required amount of blown oxygen ΔO 2 after sublance measurement is determined in this way, by stopping the oxygen supply when this ΔO 2 amount of oxygen has been blown, the end point carbon content can be adjusted to the target value CE . It will match.

なお送酸パターンとしては、低炭素鋼向の溶鋼
について第4図に示したように全吹錬期間を通じ
て一定とし、また中高炭素鋼向の溶鋼について第
5図又は第6図に示したように吹錬初期に多く、
中期から末期にかけて少くする等のパターンが従
来方法と略々同様に採られるが、サブランス計測
時点後は、送酸速度、吹込圧力等は変更しない方
が、適中率を上げるために好ましい。従つてサブ
ランス計測により(7),(8)式に基いて算出された計
測後吹錬終点までに吹込むべき酸素量ΔO2は実
質的に送酸時間で規定されることになる。つまり
ΔO2を計測時点の送酸速度で除して得た時間だ
け、計測時点から経過したときに送酸を停止す
る。第9図は上述した本発明の制御方法をフロー
チヤートにして示したものである。上述したとこ
ろから明らかな如く、この方法は制御のためのモ
デル数式を同定する第1の段階と、実操業での制
御に適用する第2の段階との2段階に大別され、
第1の段階は酸素消費速度の式(5)を得、次いで吹
込酸素量の式(7),(8)を定め、更に実操業データの
回帰分析により上記式中の定数を決定するステツ
プからなる。また第2の段階はサブランス計測を
し、これによる実測値と、吹錬終点における目標
値とを(7),(8)式に代入してΔO2を算出し、次い
でこのΔO2の送酸を行うステツプからなる。
The oxygen supply pattern is constant throughout the whole blowing period as shown in Figure 4 for molten steel for low carbon steel, and as shown in Figure 5 or 6 for molten steel for medium and high carbon steel. Often in the early stages of blowing,
A pattern such as decreasing the amount from the middle to the end is adopted almost in the same way as the conventional method, but after the sublance measurement, it is preferable not to change the oxygen supply rate, blowing pressure, etc. in order to increase the accuracy rate. Therefore, the amount of oxygen ΔO 2 that should be blown in after measurement and until the end of blowing, calculated based on equations (7) and (8) by sublance measurement, is substantially determined by the oxygen supply time. In other words, oxygen supply is stopped when the time obtained by dividing ΔO 2 by the oxygen supply rate at the time of measurement has elapsed from the time of measurement. FIG. 9 is a flowchart showing the control method of the present invention described above. As is clear from the above, this method is roughly divided into two stages: the first stage of identifying model formulas for control, and the second stage of applying them to control in actual operation.
The first step is to obtain equation (5) for the oxygen consumption rate, then determine equations (7) and (8) for the amount of blown oxygen, and then determine the constants in the above equation by regression analysis of actual operation data. Become. The second step is to perform sublance measurement, and calculate ΔO 2 by substituting the measured value and the target value at the end of blowing into equations (7) and (8), and then calculate the oxygen supply of this ΔO 2 It consists of steps to perform the following steps.

第7,8図は本発明方法を適用した場合の適中
精度を示すグラフであつて、いずれも横軸に終点
炭素含有量の目標値(%)、即ちCEを、また縦軸
にその実績値(%)をとつて表わしている。第7
図は高炭素鋼(炭素含有量0.51%以上)向の溶
鋼、第8図は中炭素鋼(炭素含有量0.21%以上
0.50%以下)向の溶鋼についての適中精度を表わ
しており、図中実線は目標値と実績値とが一致し
た場合を示す直線であり、また破線は第7図(高
炭素鋼)においては実線の±0.05%の値を示し、
第8図(中炭素鋼)においては実線の±0.03%の
値を示す直線である。図から明らかな如く、適中
率はいずれも極めて高く、高炭素鋼向けの溶鋼に
おいては、±0.05%の範囲内での適中率が41チヤ
ージ中37チヤージ、即ち90%であり、中炭素鋼向
けの溶鋼においては、±0.03%の範囲内での適中
率が48チヤージ中40チヤージ、即ち83%であつ
た。一般に終点炭素含有量の制御が難しく、適中
精度が悪いとされている中炭素鋼及び高炭素鋼向
の溶鋼において、このような高率の適中精度を得
ていることは、本発明方法の有効性を証明してい
る。
Figures 7 and 8 are graphs showing the accuracy when applying the method of the present invention, in which the horizontal axis shows the target value (%) of the end point carbon content, that is, CE , and the vertical axis shows the actual result. It is expressed as a value (%). 7th
The figure shows molten steel for high carbon steel (carbon content 0.51% or more), and Figure 8 shows medium carbon steel (carbon content 0.21% or more).
The solid line in the figure shows the straight line when the target value and actual value match, and the broken line is the solid line in Figure 7 (high carbon steel). Indicates a value of ±0.05% of
In FIG. 8 (medium carbon steel), it is a straight line that shows a value of ±0.03% of the solid line. As is clear from the figure, the accuracy rate is extremely high in all cases; for molten steel for high carbon steel, the accuracy rate within the range of ±0.05% is 37 out of 41 charges, or 90%, and for medium carbon steel. For molten steel, the accuracy within the range of ±0.03% was 40 out of 48 charges, or 83%. In molten steel for medium and high carbon steels, where it is generally difficult to control the end point carbon content and the accuracy is poor, the fact that such a high rate of accuracy has been achieved is due to the effectiveness of the method of the present invention. proves gender.

このように本発明方法による場合は吹錬終点に
おける溶鋼中の炭素含有量を極めて高精度で制御
でき、炭素含有量のダイナミツク終点制御技術の
向上に多大な貢献をなし、成分外れによる再吹錬
又は用途変更等による生産能率の悪化を防止で
き、経費削減が図れる等の実益がある。
As described above, the method of the present invention makes it possible to control the carbon content in molten steel at the end point of blowing with extremely high precision, making a great contribution to the improvement of technology for dynamic end point control of carbon content, and preventing reblowing due to component deviation. Alternatively, there are practical benefits such as preventing deterioration of production efficiency due to changes in use, etc., and reducing costs.

なお本発明方法における各種演算はプロセス制
御コンピユータに行わせ、更に自動送酸停止機能
をこのコンピユータにもたせることによつて本発
明を殆んど自動的に行わせ得ることは勿論であ
る。
It goes without saying that by having a process control computer perform various calculations in the method of the present invention, and further providing this computer with an automatic acid supply stop function, the present invention can be performed almost automatically.

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

第1図は脱炭速度と鋼中炭素含有量との関係、
第2図は酸素消費速度と鋼中炭素含有量との関係
を夫々概念的に示すグラフ、第3図は本発明に係
る数式の推定精度を実証する測定結果を示すグラ
フ、第4,5,6図は送酸パターンを表わす概念
図、第7,8図は本発明方法による終点炭素含有
量の適中精度を示すグラフ、第9図は本発明方法
の内容の概略を示すフローチヤートである。
Figure 1 shows the relationship between decarburization rate and carbon content in steel.
Fig. 2 is a graph conceptually showing the relationship between oxygen consumption rate and carbon content in steel, Fig. 3 is a graph showing measurement results demonstrating the estimation accuracy of the mathematical formula according to the present invention, Fig. 4, 5, FIG. 6 is a conceptual diagram showing the oxygen feeding pattern, FIGS. 7 and 8 are graphs showing the accuracy of the end point carbon content according to the method of the present invention, and FIG. 9 is a flowchart showing the outline of the content of the method of the present invention.

Claims (1)

【特許請求の範囲】 1 転炉操業における吹錬末期の酸素消費速度を
鋼中の炭素含有量の多項式で表わすこととし、該
多項式並びに吹錬終点前の適宜時点にてサブラン
ス計測によつて得た鋼中の炭素含有量CS、前記
時点から吹錬終点に至る間の吹込酸素量ΔO2
び吹錬終点における鋼中の炭素含有量CEを少く
とも含む実績データに基き、これらの変数の相関
関係を表わす下記数式を得ておき吹錬の都度、吹
錬終点前の適宜時点にてサブランス計測によつて
得た鋼中の炭素含有量をCS、吹錬終点における
鋼中の目標炭素含有量をCEとして、少くともこ
れらを前記数式に与えることにより、上記時点か
ら吹錬終点に至る間の所要吹込酸素量をΔO2
して算出し、この算出結果に基いて転炉操業を行
うことを特徴とする鋼中の炭素含有量制御方法。 ΔO/WST=a0(CS−CE)+a1 o(C/C)+a2〔(−1/C)−(−1/C)〕 +a3〔1/2(−1/C )−1/2(−1/C )〕+K 但し、WST:溶鋼重量 a0,a1,a2,a3:先行転炉操業の実績デー
タより得た定数 K:制御対象とする転炉操業の条件にて定
まる変数
[Scope of Claims] 1. The oxygen consumption rate at the end of blowing in converter operation is expressed by a polynomial of the carbon content in the steel, and the oxygen consumption rate obtained by sub-balance measurement at an appropriate time before the end of blowing is expressed by the polynomial and the polynomial of the carbon content in the steel. Based on actual data including at least the carbon content in the steel C S , the amount of oxygen blown from the above point to the end point of blowing ΔO 2 , and the carbon content C E in the steel at the end point of blowing, these variables are determined. Obtain the following formula that expresses the correlation between C S and the carbon content in the steel obtained by sublance measurement at an appropriate time before the end of blowing each time C S is the target value in the steel at the end of blowing. By setting the carbon content as CE and inputting at least these into the above formula, the required amount of blown oxygen from the above point to the end of blowing is calculated as ΔO 2 , and the converter operation is performed based on this calculation result. A method for controlling carbon content in steel, characterized in that: ΔO 2 /W ST = a 0 ( CSCE ) + a 1 o ( CS / CE ) + a 2 [(−1/ CS )−(−1/ CE )] + a 3 [1/2 (-1/ CS2 ) -1/2 (-1/ CE2 )]+K However , W ST : Weight of molten steel a0 , a1 , a2 , a3 : Obtained from actual data of preceding converter operation. Constant K: Variable determined by the conditions of converter operation to be controlled
JP2193480A 1980-02-21 1980-02-21 Method for controlling carbon content in steel Granted JPS56123314A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2193480A JPS56123314A (en) 1980-02-21 1980-02-21 Method for controlling carbon content in steel

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2193480A JPS56123314A (en) 1980-02-21 1980-02-21 Method for controlling carbon content in steel

Publications (2)

Publication Number Publication Date
JPS56123314A JPS56123314A (en) 1981-09-28
JPS6154843B2 true JPS6154843B2 (en) 1986-11-25

Family

ID=12068872

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2193480A Granted JPS56123314A (en) 1980-02-21 1980-02-21 Method for controlling carbon content in steel

Country Status (1)

Country Link
JP (1) JPS56123314A (en)

Also Published As

Publication number Publication date
JPS56123314A (en) 1981-09-28

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