JPH05118767A - Sintering and operating method - Google Patents

Sintering and operating method

Info

Publication number
JPH05118767A
JPH05118767A JP3279285A JP27928591A JPH05118767A JP H05118767 A JPH05118767 A JP H05118767A JP 3279285 A JP3279285 A JP 3279285A JP 27928591 A JP27928591 A JP 27928591A JP H05118767 A JPH05118767 A JP H05118767A
Authority
JP
Japan
Prior art keywords
temperature
exhaust gas
metal
value
dust collector
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
JP3279285A
Other languages
Japanese (ja)
Other versions
JP2599522B2 (en
Inventor
Yoshiaki Shimakawa
島川義明
Katsuhiko Koura
小浦克彦
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 JP3279285A priority Critical patent/JP2599522B2/en
Publication of JPH05118767A publication Critical patent/JPH05118767A/en
Application granted granted Critical
Publication of JP2599522B2 publication Critical patent/JP2599522B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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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
    • Y02P10/25Process efficiency

Abstract

PURPOSE:To prevent corrosion at a dust collector or a duct and a blower discharging gas processing system by a method wherein SO2 and H2O in the discharged gas of sinterring machine are measured, a rapid metal corrosion starting temperature is calculated in response to a result of measurement and a discharged gas temperature in the discharging gas processing system is controlled to be higher than this starting temperature. CONSTITUTION:A sinterring machine is comprised of a raw material feeding hopper 1, a sinterring machine pallet boggie 3, an air box 4, a boiler 5, dust collectors 6, 12, and discharged gas suction blowers 19, 20. Sensitive heat of the discharged gas at a rear half part of the sinterring machine is recovered by vapor at a boiler 5, resulting in that the temperature is lowered at the dust collector 6, sulfuric acid dew formation is produced within the dust collector 6 and so the dust collecting facility is apt to be corroded. In view of this fact, an SO2 meter 13, an H2O meter 14 and a thermometer 15 are mounted at an outlet side of the dust collector, a metal rapid corrosion starting temperature is calculated at 10 in reference to the SO2 value and H2O value. Boiler water feeding amount is adjusted by a water volume adjusting valve 11 in such a way as a practical temperature value is higher than the metal rapid corrosion starting temperature and the temperature of discharged gas is controlled. At the dust collector 12, the hot gas supplying damper 17 is similarly controlled.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、焼結機の排ガス顕熱回
収操業方法に関し詳しくは、前記排ガス中のSO2 とH
2 Oを検知して、排ガスの無水硫酸による金属の急腐食
開始温度を求め、前記温度以上に排ガス温度を維持する
ことで、排ガスの無水硫酸による排ガス処理装置・ダク
トの腐食防止に関する。
The present invention relates to a detail relates exhaust gas sensible heat recovery operation method of sintering machine, SO 2 and H in the flue gas
The present invention relates to the prevention of corrosion of exhaust gas treatment equipment and ducts by the sulfuric acid of exhaust gas by detecting 2 O, determining the temperature at which metal starts to be rapidly corroded by sulfuric acid of exhaust gas, and maintaining the exhaust gas temperature above the temperature.

【0002】[0002]

【従来の技術】ドワイトロイド式焼結機では、粉鉱石に
粉コークスを添加混合し、粉コークスに着火後空気を下
方に吸引し、粉コークスを燃焼させ焼き固めて焼結鉱を
製造している。
2. Description of the Related Art In a Dwightroid-type sintering machine, powdered ore is mixed with powdered coke, the powdered coke is ignited, air is sucked downward, the powdered coke is burned and solidified to produce a sintered ore. There is.

【0003】前記粉鉱石中にはS分が含まれているため
に、焼結機排ガス中にはSO2 ,SO3 が含有する。S
3 分は排ガス中のH2 Oと結合してH2 SO4 とな
り、硫酸として結露する。硫酸露点は一般的に水露点よ
り高く、かなりの高温排ガスでも結露するが、硫酸露点
温度が不明のために温度管理が出来ないままである。特
に近年、特開昭56−142830号公報で開始される
ように焼結機の高温排ガス部を熱回収して、排ガス温度
を降下させる方法では、排ガス温度が硫酸露点以下とな
り、排ガス処理設備の腐食が激しい。
Since the powdered ore contains S, SO 2 and SO 3 are contained in the exhaust gas of the sintering machine. S
The O 3 component is combined with H 2 O in the exhaust gas to form H 2 SO 4 , which is condensed as sulfuric acid. Sulfuric acid dew point is generally higher than water dew point, and even high temperature exhaust gas will condense, but temperature control cannot be done because the sulfuric acid dew point temperature is unknown. Particularly, in recent years, in a method of recovering heat from a high temperature exhaust gas portion of a sintering machine to lower the exhaust gas temperature as started in JP-A-56-142830, the exhaust gas temperature falls below the sulfuric acid dew point, and Corrosion is severe.

【0004】これらの対策として、排ガス中の水分、S
3 濃度を検出して硫酸露点以上の温度で操業するもの
として特開昭56−100654号公報が提案されてい
る。
As measures against these, water in the exhaust gas, S
Japanese Unexamined Patent Publication No. 56-100654 has been proposed to detect the O 3 concentration and operate at a temperature above the sulfuric acid dew point.

【0005】[0005]

【発明が解決しようとする課題】しかしながら、特開昭
56−100654号公報では焼結機排ガス中に存在す
る微量なSO3 濃度検出に存在する微量なSO3 量をS
3 濃度検出に有害なSO2 ,H2 O,CO,CO2
NO等が存在する焼結排ガス中では、正確なSO3 濃度
検出が不可能であること。また焼結用粉鉱石の性状、焼
結操業は常に変化しており、これにともなって排ガスの
硫酸露点も常時変化するから連続的に硫酸露点を検出す
る必要があるが、これらの良好な手段がないためにまだ
硫酸露点によるガス処理設備腐食問題は未解決の状態の
ままである。
However, in Japanese Unexamined Patent Publication No. 56-100654, the trace amount of SO 3 present in the exhaust gas of a sintering machine is detected as a trace amount of SO 3 .
SO 2 , H 2 O, CO, CO 2 , harmful to O 3 concentration detection,
It is impossible to accurately detect the concentration of SO 3 in the sintering exhaust gas containing NO and the like. In addition, since the properties of the powdered ore for sintering and the sintering operation are constantly changing, and the sulfuric acid dew point of the exhaust gas is constantly changing accordingly, it is necessary to continuously detect the sulfuric acid dew point. Therefore, the problem of corrosion of gas treatment equipment due to sulfuric acid dew point is still unsolved.

【0006】本発明は、この欠点を解決するためになさ
れたもので、焼結機排ガスの硫酸露点防止による排ガス
処理設備の腐食防止焼結操業方法を提供する。
The present invention has been made to solve this drawback, and provides a sintering operation method for preventing corrosion of exhaust gas treatment equipment by preventing sulfuric acid dew point of exhaust gas from a sintering machine.

【0007】[0007]

【課題を解決するための手段】本発明は焼結機の排ガス
顕熱回収操業方法に関し詳しくは、排ガス中のSO2
よびH2 Oを検出して、前記SO2 値およびH2 O値か
ら金属の硫酸による急腐食開始温度を求め、前記温度以
上に排ガス処理系の排ガス温度を制御する焼結操業方法
を提供するものであり、その要旨は焼結機排ガス中のS
2 およびH2Oを測定して、前記SO2 値およびH2
O値から金属の急腐食開始温度を求め、前記温度以上に
排ガス処理系の排ガス温度を制御することを特徴とする
焼結操業方法である。
The present invention relates to an exhaust gas sensible heat recovery operation method for a sintering machine. More specifically, it detects SO 2 and H 2 O in the exhaust gas, and detects the SO 2 value and the H 2 O value from the SO 2 value and the H 2 O value. The present invention provides a sintering operation method for determining the rapid corrosion start temperature of a metal by sulfuric acid and controlling the exhaust gas temperature of the exhaust gas treatment system to be higher than the above temperature.
O 2 and H 2 O were measured to determine the SO 2 value and H 2
The sintering operation method is characterized in that the rapid corrosion start temperature of the metal is obtained from the O value and the exhaust gas temperature of the exhaust gas treatment system is controlled to be equal to or higher than the above temperature.

【0008】焼結機排ガスの顕熱回収は、通常図1に示
すように、比較的温度の高い焼結機後半部の排ガスを対
象に行われるため、前半部と後半部に分割される。この
結果集麈機を通過する時の排ガス温度が、極端に低下す
るために、排ガス中のSO3がH2 Oと結合して液化
し、いわゆる硫酸結露を生じる。この結果集麈機等の腐
食を増大させる。発明者らの調査によれば、この硫酸露
点温度は一定でなく焼結操業が変化すると変わることが
判明した。この理由は、図2で示すように、焼結排ガス
中のSOX (SO2 +SO3 )発生量のピークは焼結機
後半部に偏っているが、このピークが焼結操業と共に前
後に変動するためである(詳しくはSOX中のSO3
変動するため)。このSOX 発生パターンの変動は焼結
操業の生産量、粉鉱石性状、空気吸引量等の変化にて変
わる。例えば焼結用空気吸引量が少ない場合は、焼結の
進行が遅れSOX の発生のピークも後ろの方にシフトす
る。この結果、後半に流れる排ガス中のSOX 量は増加
する。
As shown in FIG. 1, the sensible heat recovery of the exhaust gas of the sintering machine is usually performed on the exhaust gas of the latter half of the sintering machine having a relatively high temperature, so that it is divided into the first half and the second half. As a result, the exhaust gas temperature when passing through the dust collector is extremely lowered, so that SO 3 in the exhaust gas is combined with H 2 O and liquefied, so-called sulfuric acid dew condensation occurs. As a result, the corrosion of the collector and the like is increased. According to a study by the inventors, it has been found that the sulfuric acid dew point temperature is not constant and changes when the sintering operation changes. The reason for this is that, as shown in Fig. 2, the peak of the amount of SO X (SO 2 + SO 3 ) generated in the sintering exhaust gas is biased toward the latter half of the sintering machine, but this peak fluctuates back and forth with the sintering operation. This is because SO 3 in SO X fluctuates. This fluctuation of the SO X generation pattern changes depending on changes in the production amount of the sintering operation, the powder ore properties, the air suction amount, and the like. For example, if the sintering air suction amount is small, the peak of the generation of progress is delayed SO X sintering also shifted towards the back. As a result, the amount of SO X in the exhaust gas flowing in the latter half increases.

【0009】このために前半部排ガスの硫酸露点温度は
低下し、後半部排ガスの硫酸露点温度は上昇する。この
ような、硫酸露点温度の変動は焼結の通常操業で常時生
じている。
For this reason, the sulfuric acid dew point temperature of the first half exhaust gas decreases, and the sulfuric acid dew point temperature of the second half exhaust gas rises. Such fluctuations in the sulfuric acid dew point temperature always occur in the normal operation of sintering.

【0010】従って排ガス処理設備への硫酸結露を防止
するためには、刻々と変化する硫酸露点温度を常時検知
し、前記露点温度より、高い温度に排ガス温度を維持す
る必要がある。硫酸露点温度を求める方法として従来は
排ガス中のSO2 +SO3 を全硫黄酸化物分析(JIS
K0103)で、またSO2 を二酸化硫黄自動計測器
(JIS B7981)で測定し、前記測定値のSO2
+SO3 からSO2 を差し引いた残りをSO3 とし、こ
のSO3 値から計算によって酸露点温度を求めていた。
通常排ガス温度をこの酸露点温度以下にすると硫酸結露
による金属の腐食が急増するが、発明者が実際に種々の
SOX 値の焼結排ガス中に易腐食性金属を暴露し、腐食
が急増する温度を求めた値と前記の方法で求めた酸露点
温度に大きな隔たりがあることが判明した。その結果を
図3に示した。
Therefore, in order to prevent the sulfuric acid dew condensation on the exhaust gas treatment equipment, it is necessary to constantly detect the sulfuric acid dew point temperature which changes every moment and maintain the exhaust gas temperature higher than the dew point temperature. Conventionally, SO 2 + SO 3 in exhaust gas is analyzed by total sulfur oxide analysis (JIS
K0103) and SO 2 were measured by a sulfur dioxide automatic measuring device (JIS B7981), and the measured value of SO 2 was measured.
The remainder obtained by subtracting SO 2 from + SO 3 was taken as SO 3, and the acid dew point temperature was calculated from this SO 3 value.
When the normal exhaust gas temperature below the acid dew point temperature increases rapidly corrosion of metals by sulfuric acid condensation, but the inventors actually exposing the easily corrosive metal during the sintering exhaust gas various SO X value, corrosion increases rapidly It was found that there was a large difference between the value obtained by measuring the temperature and the acid dew point temperature obtained by the above method. The results are shown in Fig. 3.

【0011】図から判るように従来法の酸露点温度と金
属の腐食開始温度には、大きな隔たりがある。しかも、
両値の差は一定ではなく大小さまざまである。このこと
から従来法で求めた酸露点温度は正確でないことが判
る。
As can be seen from the figure, there is a large difference between the acid dew point temperature of the conventional method and the corrosion start temperature of the metal. Moreover,
The difference between the two values is not constant and varies in magnitude. This shows that the acid dew point temperature obtained by the conventional method is not accurate.

【0012】また、従来法で求めた硫酸露点温度は、本
発明法の温度より比較的高く、この方法では排ガス温度
を大きく下げることは困難であり排熱回収量は少なくな
る。この排熱回収量をより多くするためには従来法で求
めた硫酸露点温度より低い金属の急腐食開始温度を求
め、この温度以上で操業することが望ましい。
Further, the sulfuric acid dew point temperature obtained by the conventional method is relatively higher than the temperature of the method of the present invention, and it is difficult to greatly reduce the exhaust gas temperature by this method, and the amount of exhaust heat recovery becomes small. In order to increase this amount of exhaust heat recovery, it is desirable to obtain a rapid corrosion start temperature of the metal that is lower than the sulfuric acid dew point temperature obtained by the conventional method, and to operate above this temperature.

【0013】発明者らは、数々の実験によりこの金属の
急腐食開始温度が排ガス中のSO2量とH2 O量に関係
することをつきとめた。その関係を図4に示す。
The inventors have found by various experiments that the rapid corrosion initiation temperature of this metal is related to the amounts of SO 2 and H 2 O in the exhaust gas. The relationship is shown in FIG.

【0014】例えば排ガス中のSO2 量が100ppm
で、H2 O量が10%であれば金属の急腐食開始温度は
90℃であり、この温度より高い値に排ガス温度を維持
することで金属製の排ガス処理用設備及び配管の腐食を
防止することが出来る。
For example, the amount of SO 2 in the exhaust gas is 100 ppm
Therefore, if the amount of H 2 O is 10%, the rapid corrosion start temperature of the metal is 90 ° C, and by maintaining the exhaust gas temperature higher than this temperature, the corrosion of metal exhaust gas treatment equipment and piping is prevented. You can do it.

【0015】この場合に金属が腐食する要因は排ガス中
のSO2 ではなくSO3 がH2 Oと反応して硫酸となり
金属表面に結露するためである。従って、金属の急腐食
開始温度はSO2 濃度から下記(1)式を用いてSO3
を推定し、前記SO3 と排ガス中のH2 O値から下記
(2)式を用いて金属の急腐食開始温度を求めるもので
ある。
The cause of metal corrosion in this case is that SO 3 in the exhaust gas, not SO 2 , reacts with H 2 O to form sulfuric acid, which condenses on the metal surface. Thus, rapid corrosion initiation temperature of the metal by using the following equation (1) from the SO 2 concentration SO 3
Is calculated, and the rapid corrosion start temperature of the metal is calculated from the SO 3 and the H 2 O value in the exhaust gas using the following equation (2).

【0016】[0016]

【数1】 [Equation 1]

【0017】つまり、本発明のポイントは焼結排ガスに
おいてSO2 とSO3 の関係を見出し、これを定量化
し、最終的に金属の急腐食開始温度を求めるものであ
る。
That is, the point of the present invention is to find out the relationship between SO 2 and SO 3 in the sintering exhaust gas, quantify this, and finally obtain the rapid corrosion start temperature of the metal.

【0018】排ガス温度を制御する方法としては、例え
ば焼結機前半部の低温排ガスにおいては、低温排ガス中
に焼結機最後部の高温排ガスの混入量を変化させること
で可能である。また焼結機後半部の高温排ガスの顕熱を
変化させることで、排ガス温度を制御することが出来る
ものであり、他のバーナでの加熱、および蒸気加熱等を
用いても良い。
As a method of controlling the exhaust gas temperature, for example, in the low temperature exhaust gas in the first half of the sintering machine, it is possible to change the mixing amount of the high temperature exhaust gas in the rearmost part of the sintering machine in the low temperature exhaust gas. The exhaust gas temperature can be controlled by changing the sensible heat of the high-temperature exhaust gas in the latter half of the sintering machine, and heating with another burner, steam heating, or the like may be used.

【0019】ここで言う金属の急腐食開始温度とは、水
露点温度より高い値でしかも排ガス中のSO3 とH2
が反応して硫酸を作り金属表面に付着して、この硫酸に
よって金属が腐食を開始する温度である。次に本発明を
実施例を用いて説明する。
The term "rapid corrosion initiation temperature of metal" as used herein means a value higher than the water dew point temperature and SO 3 and H 2 O in exhaust gas.
Reacts to form sulfuric acid and adheres to the metal surface, and this sulfuric acid is the temperature at which the metal begins to corrode. Next, the present invention will be described using examples.

【0020】[0020]

【実施例】本発明の実施例について以下説明する。図5
は本発明を実施するための焼結機の略側面図である。図
において、1は原料挿入ホッパー、2は点火炉、3は焼
結機パレット台車、4は風箱、5はボイラー、6は集麈
機、7はSO2 計、8はH2 O計、9は温度計、10は
演算機、11は水量調整弁、12は集麈機、13はSO
2 計、14はH2 O計、15は温度計、16は演算機、
17は高温排ガス供給ダンパー、18は高温ガスバイパ
スダクト、19は排ガス吸引ブロワー、20は排ガス吸
引ブロワーである。
EXAMPLES Examples of the present invention will be described below. Figure 5
FIG. 3 is a schematic side view of a sintering machine for carrying out the present invention. In the figure, 1 is a raw material insertion hopper, 2 is an ignition furnace, 3 is a pallet truck for a sintering machine, 4 is a wind box, 5 is a boiler, 6 is a collector, 7 is an SO 2 meter, 8 is an H 2 O meter, 9 is a thermometer, 10 is a calculator, 11 is a water flow control valve, 12 is a collector, and 13 is SO.
2 meters, 14 is an H 2 O meter, 15 is a thermometer, 16 is a calculator,
Reference numeral 17 is a high temperature exhaust gas supply damper, 18 is a high temperature gas bypass duct, 19 is an exhaust gas suction blower, and 20 is an exhaust gas suction blower.

【0021】比較的高温である焼結機の後半部排ガスの
顕熱はボイラー5で蒸気によって回収されるためボイラ
ー後の集麈機部6では温度が降下している。この時集麈
機出口の温度が金属の急腐食開始温度より低い場合は集
麈機内で硫酸結露を生じ、集麈機設備が腐食する。これ
を防止するために集麈機出側にSO2 計7とH2 O計8
と温度計9を設置しSO2 メーターのSO2 値とH2
計のH2 O値から金属の急腐食開始温度を演算機10で
計算し、前記温度計の値が金属の急腐食開始温度以上と
なるようにボイラーに入る水量を水量調整弁11で調整
する。
Since the sensible heat of the exhaust gas in the latter half of the sintering machine, which is relatively high temperature, is recovered by the steam in the boiler 5, the temperature is lowered in the collector unit 6 after the boiler. At this time, if the temperature at the exit of the collector is lower than the rapid corrosion start temperature of the metal, sulfuric acid dew will be generated in the collector, and the collector equipment will be corroded. In order to prevent this, SO 2 meter 7 and H 2 O meter 8 are installed on the exit side of the collector.
SO 2 value of the thermometer 9 installed SO 2 meter and H 2 O
The rapid corrosion start temperature of the metal is calculated by the calculator 10 from the H 2 O value of the meter, and the amount of water entering the boiler is adjusted by the water amount adjusting valve 11 so that the value of the thermometer becomes equal to or higher than the rapid corrosion start temperature of the metal. .

【0022】また比較的低温である。焼結機の前半排ガ
スは排ガスダクトをへて、集麈機12を通るが、集麈機
出口の温度が金属の急腐食開始温度より、低い場合は、
集麈機内で硫酸結露を生じ、集麈設備が腐食する。これ
を防止するために集麈機出側にSO2 計13とH2 O計
14と温度計15を設置しSO2 メーターのSO2 値と
2 O計のH2 O値から金属の急腐食開始温度を演算機
16で計算し、前記温度計の値が金属の急腐食開始温度
以上となるように高温排ガス供給ダンパー17を調整
し、高温排ガス量を高温ガスバイパスダクト18を介し
変化させる。
The temperature is relatively low. Exhaust gas in the first half of the sintering machine passes through the exhaust gas duct and passes through the collector 12, but when the temperature at the exit of the collector is lower than the rapid corrosion start temperature of the metal,
Sulfuric acid is condensed in the collector and the collector equipment is corroded. Suddenly from H 2 O values established the SO 2 meter 13 and H 2 O meter 14 and thermometer 15 in the outlet side current麈機SO 2 value of SO 2 meter and H 2 O gauge metal in order to prevent this The corrosion start temperature is calculated by the computer 16, the high temperature exhaust gas supply damper 17 is adjusted so that the value of the thermometer becomes equal to or higher than the rapid corrosion start temperature of the metal, and the high temperature exhaust gas amount is changed via the high temperature gas bypass duct 18. .

【0023】これらの実施により、排ガス処理設備また
はダクト内への硫酸結露が無くなり、設備の腐食が防止
される。
By implementing these, the sulfuric acid condensation in the exhaust gas treatment equipment or the duct is eliminated, and the equipment is prevented from corrosion.

【0024】[0024]

【発明の効果】以上説明した如く、本発明のSO2 値お
よびH2 O値を検出して、金属の急腐食開始温度を求
め、前記金属の急腐食開始温度以上に排ガス温度を保つ
ことで集麈機やダクトおよびブロワーなど排ガス処理系
統の腐食が皆無となり、前記設備の寿命が大巾に延び
る。
As described above, the SO 2 value and the H 2 O value of the present invention are detected to determine the rapid corrosion start temperature of the metal, and the exhaust gas temperature is kept above the rapid corrosion start temperature of the metal. Corrosion of the exhaust gas treatment system such as the collector and the duct and the blower is completely eliminated, and the life of the equipment is greatly extended.

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

【図1】従来技術を説明する焼結機の排ガス処理フロー
図。
FIG. 1 is an exhaust gas treatment flow chart of a sintering machine for explaining a conventional technique.

【図2】焼結機のSOX 発生パターン図。FIG. 2 is a SO X generation pattern diagram of the sintering machine.

【図3】従来法による硫酸露点温度と本発明の金属の急
腐食開始温度の比較図。
FIG. 3 is a comparison diagram of the sulfuric acid dew point temperature by the conventional method and the rapid corrosion start temperature of the metal of the present invention.

【図4】焼結機排ガス中のSO2 量と金属の急腐食開始
温度の関係図。
FIG. 4 is a diagram showing the relationship between the amount of SO 2 in the exhaust gas from the sintering machine and the rapid corrosion start temperature of metal.

【図5】本発明を実施するための焼結機排ガス処理フロ
ー図。
FIG. 5 is a flow chart of exhaust gas treatment of a sintering machine for carrying out the present invention.

【符号の説明】[Explanation of symbols]

1…原料挿入ホッパー 2…点火炉 3…焼結機パレット台車 4…風箱 5…ボイラー 6…集麈機 7…SO2 計 8…H2 O計 9…温度計 10…演算機 11…水量調整弁 12…集麈機 13…SO2 計 14…H2 O計 15…温度計 16…演算機 17…高温排ガス供給ダンパー 18…高温ガスバイ
パスダクト 19…排ガス吸引ブロワー 20…排ガス吸引ブ
ロワー
1 ... Raw material insertion hopper 2 ... Ignition furnace 3 ... Sintering machine pallet trolley 4 ... Wind box 5 ... Boiler 6 ... Collecting machine 7 ... SO 2 meter 8 ... H 2 O meter 9 ... Thermometer 10 ... Computing machine 11 ... Water amount Control valve 12 ... Collector 13 ... SO 2 meter 14 ... H 2 O meter 15 ... Thermometer 16 ... Computing machine 17 ... High temperature exhaust gas supply damper 18 ... High temperature gas bypass duct 19 ... Exhaust gas suction blower 20 ... Exhaust gas suction blower

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 焼結機排ガス中のSO2 およびH2 Oを
測定して、前記SO2 値およびH2 O値から金属の急腐
食開始温度を求め、前記温度以上に排ガス処理系の排ガ
ス温度を制御することを特徴とする焼結操業方法。
1. SO 2 and H 2 O in the exhaust gas of the sintering machine are measured, the rapid corrosion start temperature of the metal is determined from the SO 2 value and H 2 O value, and the exhaust gas of the exhaust gas treatment system is heated to a temperature above the temperature. A sintering operation method characterized by controlling temperature.
JP3279285A 1991-10-25 1991-10-25 Sintering operation method Expired - Lifetime JP2599522B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3279285A JP2599522B2 (en) 1991-10-25 1991-10-25 Sintering operation method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3279285A JP2599522B2 (en) 1991-10-25 1991-10-25 Sintering operation method

Publications (2)

Publication Number Publication Date
JPH05118767A true JPH05118767A (en) 1993-05-14
JP2599522B2 JP2599522B2 (en) 1997-04-09

Family

ID=17609040

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3279285A Expired - Lifetime JP2599522B2 (en) 1991-10-25 1991-10-25 Sintering operation method

Country Status (1)

Country Link
JP (1) JP2599522B2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101832572A (en) * 2010-03-19 2010-09-15 湖南永清环保股份有限公司 Method for leading flue gas out of sintering flue gas waste heat utilization system without using induced draft fan
JP2012193909A (en) * 2011-03-17 2012-10-11 Kawasaki Heavy Ind Ltd Waste heat recovery power generation plant for sintering facility
JP2012251698A (en) * 2011-06-01 2012-12-20 Jp Steel Plantech Co Waste heat recovery equipment of sintered ore cooling device, waste heat recovering method, and sintering machine system

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56100654A (en) * 1980-01-17 1981-08-12 Nippon Steel Corp Treatment of sintering exhaust gas

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56100654A (en) * 1980-01-17 1981-08-12 Nippon Steel Corp Treatment of sintering exhaust gas

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101832572A (en) * 2010-03-19 2010-09-15 湖南永清环保股份有限公司 Method for leading flue gas out of sintering flue gas waste heat utilization system without using induced draft fan
JP2012193909A (en) * 2011-03-17 2012-10-11 Kawasaki Heavy Ind Ltd Waste heat recovery power generation plant for sintering facility
JP2012251698A (en) * 2011-06-01 2012-12-20 Jp Steel Plantech Co Waste heat recovery equipment of sintered ore cooling device, waste heat recovering method, and sintering machine system

Also Published As

Publication number Publication date
JP2599522B2 (en) 1997-04-09

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