JPH0535349B2 - - Google Patents
Info
- Publication number
- JPH0535349B2 JPH0535349B2 JP25405484A JP25405484A JPH0535349B2 JP H0535349 B2 JPH0535349 B2 JP H0535349B2 JP 25405484 A JP25405484 A JP 25405484A JP 25405484 A JP25405484 A JP 25405484A JP H0535349 B2 JPH0535349 B2 JP H0535349B2
- Authority
- JP
- Japan
- Prior art keywords
- temperature
- raw material
- gas
- heat
- melting
- 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 - Lifetime
Links
- 239000007789 gas Substances 0.000 claims description 84
- 239000002994 raw material Substances 0.000 claims description 66
- 238000002844 melting Methods 0.000 claims description 38
- 230000008018 melting Effects 0.000 claims description 38
- 238000000034 method Methods 0.000 claims description 14
- 239000003575 carbonaceous material Substances 0.000 claims description 12
- 238000011084 recovery Methods 0.000 claims description 11
- 238000006243 chemical reaction Methods 0.000 claims description 9
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 7
- 229910052760 oxygen Inorganic materials 0.000 claims description 7
- 239000001301 oxygen Substances 0.000 claims description 7
- -1 scrap Substances 0.000 claims description 2
- 238000002485 combustion reaction Methods 0.000 description 28
- 229910000831 Steel Inorganic materials 0.000 description 6
- 239000010959 steel Substances 0.000 description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 239000000428 dust Substances 0.000 description 4
- 239000003245 coal Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 239000003209 petroleum derivative Substances 0.000 description 2
- 238000010079 rubber tapping Methods 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 239000000567 combustion gas Substances 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
Landscapes
- Manufacture And Refinement Of Metals (AREA)
- Waste-Gas Treatment And Other Accessory Devices For Furnaces (AREA)
- Furnace Details (AREA)
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は、スクラツプ等の溶解方法に係り、特
に、省電力化と排ガスの顕熱と潛熱との有効利用
を達成することができるスクラツプ等の溶解方法
に関する。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a method for melting scrap, etc., and in particular, to a method for melting scrap, etc., which can achieve power saving and effective use of sensible heat and heat from exhaust gas. Concerning a method of dissolving.
[従来の技術]
一般にスクラツプ等の固体の鉄を再利用するた
めに、これを溶解する装置として、三相電極のア
ーク熱を利用する三相アーク炉はすでに知られて
いる。[Prior Art] A three-phase arc furnace that utilizes the arc heat of three-phase electrodes is already known as a device for melting solid iron, such as scrap, in order to recycle it.
このアーク炉は、上方が開放されたアーク炉本
体内に原料スクラツプを投入しておき、これに三
相電極を挿入しつつ上蓋をして放電させ、このア
ーク熱により原料を溶解するようにしたものであ
る。そして、このアーク炉本体から発生する排ガ
スは周辺部より炉内に侵入した空気を主成分とす
るが一部CO等の可燃分を含んでいるため、排ガ
スを炉内より取出してこれを燃焼し、この燃焼ガ
スにより原料スクラツプを予熱して熱の有効利用
を図つている。 In this arc furnace, raw material scrap is placed in the arc furnace main body, which is open at the top, and a three-phase electrode is inserted into this, the top lid is placed on it, and the raw material is discharged, and the raw material is melted by the arc heat. It is something. The exhaust gas generated from the arc furnace body is mainly composed of air that has entered the furnace from the surrounding area, but it also contains some combustible components such as CO, so the exhaust gas is taken out from inside the furnace and burned. This combustion gas is used to preheat the raw material scrap, making effective use of heat.
[発明が解決しようとする問題点]
ところで、従来の溶解方法の如くアーク熱でス
クラツプ等の原料を溶解する場合には、排ガスで
予熱を行なつているといえども多量の電力を必要
とし、特に我国のように電気料の高い国において
は、操業コストの高騰を余儀なくされていた。[Problems to be Solved by the Invention] By the way, when melting raw materials such as scrap using arc heat as in the conventional melting method, a large amount of electric power is required even though preheating is performed using exhaust gas. Especially in countries like Japan where electricity costs are high, operating costs have been forced to rise.
そこで、溶解のために、電気エネルギと油、石
油ガスとを併用することも行なわれてはいるが、
油、石油ガス等も高価であり、操業コストを充分
に低減することはできない。 Therefore, although electrical energy and oil or petroleum gas are used together for melting,
Oil, petroleum gas, etc. are also expensive, and operating costs cannot be reduced sufficiently.
また、溶解時に発生する高温排ガスで他の原料
を予熱してはいるが、この排ガス温度は約600度
前後と低く、従つて原料の予熱温度も200〜300度
と更に低くなつて十分な予熱を行なうことができ
ない。 In addition, other raw materials are preheated using the high-temperature exhaust gas generated during melting, but the temperature of this exhaust gas is low at around 600 degrees, so the preheating temperature of the raw materials is even lower at 200 to 300 degrees, making it difficult to preheat them sufficiently. can't do it.
また、排ガス中に含まれる可燃ガスを燃焼する
ことも行なわれてはいるが、可燃ガスの含有率は
非常に低く排ガスを充分に温度上昇させることが
できない。 Furthermore, although combustion of combustible gas contained in the exhaust gas has been carried out, the content of combustible gas is very low and the temperature of the exhaust gas cannot be raised sufficiently.
更には、前述の如く原料の予熱温度が低いこと
から、原料中に含まれる有機分の熱分解により発
生する悪臭成分が公害の発生源となつていた。 Furthermore, as mentioned above, since the preheating temperature of the raw materials is low, malodorous components generated by thermal decomposition of organic components contained in the raw materials have become a source of pollution.
特にスクラツプ消費量が今後大きく増加するこ
とが予想される今日において、上記した問題点の
解決が早期に望まれている。 Particularly in today's world where scrap consumption is expected to increase significantly in the future, it is desired to solve the above-mentioned problems as soon as possible.
[発明の目的]
本発明は以上のような問題点に着目し、これを
有効に解決すべく創案されたものである。[Object of the Invention] The present invention has focused on the above-mentioned problems and has been devised to effectively solve the problems.
本発明の目的は、溶解炉内に炭材を酸素又は空
気とともに吹込むことにより可燃ガス生成反応を
させてその反応熱で原料溶解を行ない、そして、
排出される可燃ガスから顕熱及び潛熱を順次回収
するようにし、もつて消費電力を大幅に削減する
ことができるスクラツプ等の溶解方法に関する。 The purpose of the present invention is to cause a combustible gas producing reaction by blowing carbonaceous material into a melting furnace together with oxygen or air, and to melt the raw material using the reaction heat, and
The present invention relates to a method for melting scrap, etc., which sequentially recovers sensible heat and radiant heat from emitted combustible gas, thereby significantly reducing power consumption.
[発明の概要]
上記目的を達成する本発明の構成は、まず、溶
解炉内へ炭材を空気などと共に吹込むことによ
り、この炭材を酸素と反応させて、可燃性ガス例
えばCO,H2等を生成させて、この反応熱により
装入原料を溶解し、次いで排出される高温可燃ガ
スを1次原料予熱器へ導入してこの中に装入され
ている原料を予熱することにより顕熱を回収し、
更に、顕熱回収後の可燃ガスを燃焼させて得られ
る高温排ガスを2次原料予熱器へ導入して、この
中へ装入されている他の原料を高温予熱すること
により潛熱を回収するようにし、もつて排ガスの
顕熱、潛熱を有効に利用するようにしたことを要
旨とする。[Summary of the Invention] The structure of the present invention that achieves the above object is as follows: First, carbonaceous material is blown into a melting furnace together with air, and the carbonaceous material is reacted with oxygen to generate combustible gases such as CO, H, etc. 2, etc., the charged raw material is melted by this reaction heat, and then the discharged high temperature combustible gas is introduced into the primary raw material preheater to preheat the raw material charged therein. recover heat,
Furthermore, the high-temperature exhaust gas obtained by burning the combustible gas after sensible heat recovery is introduced into the secondary raw material preheater, and the other raw materials charged therein are preheated at a high temperature, thereby recovering the residual heat. The main point is that the sensible heat and heat of the exhaust gas are effectively utilized.
[実施例]
以下に、本発明方法を添付図面に基づいて詳述
する。[Example] Below, the method of the present invention will be explained in detail based on the accompanying drawings.
第1図は本発明方法を実施するための溶解炉設
備を示す概略平面図である。 FIG. 1 is a schematic plan view showing melting furnace equipment for carrying out the method of the present invention.
図示する如くこの溶解炉設備は装入原料を溶解
する溶解炉1と、溶解時に発生する高温可燃ガス
から顕熱を回収する第1原料予熱器2と、顕熱回
収後の可燃ガスを燃焼する燃焼塔3と、これより
排出される高温排ガスにより他の原料を高温予熱
して潛熱を回収する第2原料予熱器4とにより主
に構成されている。 As shown in the figure, this melting furnace equipment includes a melting furnace 1 that melts charged raw materials, a first raw material preheater 2 that recovers sensible heat from high-temperature combustible gas generated during melting, and a first raw material preheater 2 that burns the combustible gas after recovering the sensible heat. It mainly consists of a combustion tower 3 and a second raw material preheater 4 that preheats other raw materials at a high temperature using high-temperature exhaust gas discharged from the combustion tower 3 and recovers heat from the combustion tower.
溶解炉1の炉蓋5の上方には炉内へ挿脱自在に
なされた電極6を備えると共に、溶解時に生成さ
れた可燃性の高温ガスを炉外へ排出するための高
温ガス排出口7が形成されている。また炉の底部
側壁には炉内で生成した溶鋼を取出すための出鋼
口8が形成されると共に炉の底部には微粉炭等の
炭材を酸素又は空気とともに炉内へ吹込むための
炭材吹込口9が形成されている。 Above the furnace lid 5 of the melting furnace 1, there is an electrode 6 that can be inserted into and removed from the furnace, and a high-temperature gas discharge port 7 for discharging flammable high-temperature gas generated during melting to the outside of the furnace. It is formed. In addition, a tapping port 8 is formed on the bottom side wall of the furnace to take out the molten steel produced in the furnace, and a carbon material injection port 8 is formed at the bottom of the furnace to blow carbon material such as pulverized coal into the furnace together with oxygen or air. A mouth 9 is formed.
上記溶解炉1の高温ガス排出口7は、高温可燃
ガス通路10を介して1次原料予熱器2のガス導
入口11に連絡されている。また、1次原料予熱
器2のガス排出口12は燃焼塔3のガス入口13
に通路14を介して連絡されており、塔内に導入
した可燃ガスを燃焼するようになつている。燃焼
塔3のガス出口15は高温排ガス通路16を介し
て2次原料予熱器4の高温排ガス導入口17に連
絡されている。この2次原料予熱器4のガス排出
口18は、上記燃焼塔3内で用いる燃焼用空気を
予熱するための燃焼用空気予熱器19のガス入口
20へ低温ガス通路21を介して連絡されてい
る。燃焼用空気予熱器19のガス出口22は、途
中に送風フアン23が介設されたガス通路24を
介して集じん器25のガス入口26へ連絡され、
この集じん器25で除じんされた排ガスをガス出
口27から系外へ排出するようになつている。 The high-temperature gas outlet 7 of the melting furnace 1 is connected to the gas inlet 11 of the primary raw material preheater 2 via a high-temperature combustible gas passage 10. Further, the gas outlet 12 of the primary raw material preheater 2 is connected to the gas inlet 13 of the combustion tower 3.
The tower is connected to the tower through a passage 14, and the combustible gas introduced into the tower is combusted. A gas outlet 15 of the combustion tower 3 is connected to a high temperature exhaust gas inlet 17 of the secondary raw material preheater 4 via a high temperature exhaust gas passage 16. The gas outlet 18 of the secondary raw material preheater 4 is connected via a low temperature gas passage 21 to the gas inlet 20 of a combustion air preheater 19 for preheating the combustion air used in the combustion tower 3. There is. A gas outlet 22 of the combustion air preheater 19 is connected to a gas inlet 26 of a dust collector 25 via a gas passage 24 in which a blower fan 23 is interposed.
The exhaust gas from which dust has been removed by the dust collector 25 is discharged out of the system from a gas outlet 27.
次に以上のように構成された溶解炉設備に基づ
いて本発明方法を具体的に説明する。 Next, the method of the present invention will be specifically explained based on the melting furnace equipment configured as described above.
まず、溶解炉1内にこの底部に設けた炭材吹込
口9から微粉炭、チヤー、コークス等の炭材を酸
素又は空気とともに吹込む。この溶解炉1内には
アーク熱により或いは前工程で生成した溶鋼を少
し残留させるなどして初期溶鋼を予め形成してお
く。吹込まれた酸素分は溶鉄中に吹込まれた炭素
とともに発熱反応を起し、CO,H2、炭化水素系
の可燃ガスを発生させる。この時発生する熱量に
より装入原料を昇熱し、溶解する。 First, a carbon material such as pulverized coal, char, or coke is injected into the melting furnace 1 from a carbon material inlet 9 provided at the bottom of the melting furnace 1 together with oxygen or air. Initial molten steel is previously formed in the melting furnace 1 by arc heat or by leaving a small amount of molten steel produced in a previous process. The injected oxygen causes an exothermic reaction with the carbon injected into the molten iron, generating CO, H 2 and hydrocarbon-based combustible gases. The amount of heat generated at this time heats up the charged raw material and melts it.
そして、発生した高温可燃ガスは約600℃前後
となり、高温ガス排出口7から排出されて高温可
燃ガス通路10を通り、1次原料予熱器2内へ導
入される。この1次原料予熱器2内には予め他の
原料が装入されており、この原料を上記高温可燃
ガスにより1次予熱して排ガスの保有する顕熱を
回収する。この1次予熱においては、熱源となる
高温可燃ガス温度が約600℃と比較的低いために
原料を200〜300℃まで予熱できるにすぎない。そ
して、この予熱された原料はその後前記溶解炉1
内へ移送されて、溶解されることになる。上記1
次予熱においては、予熱温度が低いことから原料
に含まれる有機分が分解して悪臭成分を生成する
こととなるが、この悪臭成分は可燃ガスとともに
後流側へ搬送されることになる。 The generated high-temperature combustible gas has a temperature of about 600° C. and is discharged from the high-temperature gas outlet 7, passes through the high-temperature combustible gas passage 10, and is introduced into the primary raw material preheater 2. Other raw materials are charged in advance into the primary raw material preheater 2, and this raw material is primarily preheated with the above-mentioned high temperature combustible gas to recover the sensible heat possessed by the exhaust gas. In this primary preheating, the temperature of the high-temperature combustible gas serving as the heat source is relatively low at about 600°C, so the raw material can only be preheated to 200 to 300°C. Then, this preheated raw material is then transferred to the melting furnace 1.
It will be transported inside and dissolved. Above 1
In the next preheating, since the preheating temperature is low, organic components contained in the raw materials are decomposed to produce malodorous components, but these malodorous components are transported to the downstream side together with the combustible gas.
すなわち、1次原料予熱器2のガス排出口12
から排出される顕熱回収後の可燃ガス中には悪臭
成分が含まれており、この可燃ガスは通路14を
介してガス入口13から燃焼塔3内へ導入され、
導入されたこの可燃ガスは燃焼用空気予熱器19
側から供給される燃焼用空気により燃焼されて約
1000℃前後の高温排ガスとなる。この際、1次原
料予熱器2から可燃ガスとともに搬送されてきた
悪臭成分は燃焼塔3内の高熱のために熱分解され
て悪臭となる。 That is, the gas outlet 12 of the primary raw material preheater 2
The combustible gas discharged from the combustion chamber after sensible heat recovery contains malodorous components, and this combustible gas is introduced into the combustion tower 3 from the gas inlet 13 via the passage 14,
This combustible gas introduced into the combustion air preheater 19
Burned by combustion air supplied from the side, approximately
The result is high-temperature exhaust gas of around 1000℃. At this time, the malodorous components conveyed together with the combustible gas from the primary raw material preheater 2 are thermally decomposed due to the high heat within the combustion tower 3 and become malodorous.
ここで、発生する高温ガスは燃焼塔3のガス出
口15から排出された後、高温排ガス通路16内
を流れ、高温排ガス導入口17から2次原料予熱
器4内に導入される。この2次原料予熱器4内に
おいては、予め更に他の原料が装入されており、
この原料を上記高温排ガスにより2次予熱して潛
熱の回収を行なう。この2次予熱の熱源となる高
温排ガスは約1000℃と特に高く、従つてこの予熱
器4内に装入されていた原料は600〜800℃前後の
高温にまで予熱されることになる。また、この高
温予熱時に発生する悪臭成分は、この2次予熱自
体が800℃以上の高温状態で行なわれるために、
直ちに熱分解される。 Here, the generated high-temperature gas is discharged from the gas outlet 15 of the combustion tower 3, flows through the high-temperature exhaust gas passage 16, and is introduced into the secondary raw material preheater 4 through the high-temperature exhaust gas inlet 17. In this secondary raw material preheater 4, other raw materials are charged in advance,
This raw material is secondarily preheated using the high-temperature exhaust gas to recover heat from the heat. The high-temperature exhaust gas that is the heat source for this secondary preheating is particularly high at about 1000°C, so the raw material charged in the preheater 4 is preheated to a high temperature of about 600 to 800°C. In addition, the malodorous components generated during this high-temperature preheating are caused by the fact that the secondary preheating itself is carried out at a high temperature of 800°C or higher.
Immediately thermally decomposed.
このように潛熱回収がなされて比較的低温とな
つたガスは、2次原料予熱器4のガス排出口18
から排出されて低温ガス通路21を流れ、ガス入
口20より燃焼用空気予熱器19内へ導入され
る。この導入された排ガスは外気温と比較したら
未だ高温なので、この排ガスの保有する顕熱によ
り前記燃焼塔3で使用する燃焼用空気を予熱し、
更に熱回収を行なう。ここで予熱された燃焼用空
気は、通路28を介して前述の如く燃焼塔3内へ
導入されて可燃ガスの燃焼に寄与する。 The gas, which has become relatively low in temperature due to the heat recovery, is transferred to the gas outlet 18 of the secondary raw material preheater 4.
It flows through the low temperature gas passage 21 and is introduced into the combustion air preheater 19 through the gas inlet 20. Since this introduced exhaust gas is still at a high temperature compared to the outside temperature, the combustion air used in the combustion tower 3 is preheated by the sensible heat possessed by this exhaust gas,
Furthermore, heat recovery is performed. The combustion air preheated here is introduced into the combustion tower 3 through the passage 28 as described above and contributes to the combustion of combustible gas.
一方、燃焼用空気予熱器19から排出された排
ガスはガス通路24を流れ、送風フアン23及び
集じん器25を通過した後、大気中へ放出され
る。 On the other hand, the exhaust gas discharged from the combustion air preheater 19 flows through the gas passage 24, passes through the blower fan 23 and the dust collector 25, and is then discharged into the atmosphere.
このようにして、溶解炉1内で原料の溶解を行
ないつつ溶解により発生した高温可燃ガスから顕
熱回収及び潛熱回収を行なつて溶解作業を終了す
ると、その溶鋼を出鋼口8から取出し、更に空に
なつた溶解炉1に1次原料予熱器2又は2次原料
予熱器4内で低温予熱或いは高温予熱した原料を
装入して前記と同様に溶解を行なう。 In this way, while melting the raw materials in the melting furnace 1, sensible heat recovery and radiant heat recovery are performed from the high-temperature combustible gas generated by the melting, and when the melting work is completed, the molten steel is taken out from the tapping port 8, Furthermore, raw materials preheated at a low temperature or at a high temperature in the primary raw material preheater 2 or the secondary raw material preheater 4 are charged into the now empty melting furnace 1 and melted in the same manner as described above.
このように、本発明方法においては、まず、溶
鋼炉内へ炭材を空気などと共に吹込むことによ
り、この炭材を酸素と可燃ガス生成反応させてこ
の反応熱により装入原料を溶解し、次いで排出さ
れる高温可燃ガスを1次原料予熱器へ導入して、
この中に装入されている原料を予熱することによ
り顕熱を回収し、更に、顕熱回収後の可燃排ガス
を燃焼させて得られる高温排ガスを2次原料予熱
器へ導入して、この中に装入されている他の原料
を高温予熱することにより潛熱を回収するように
したので、全工程を通じてアーク加熱を行なう必
要がなく使用するとしても初期溶鋼生成時だけで
済み、消費電力を大幅に削減することができる。 As described above, in the method of the present invention, first, carbonaceous material is blown into a steel melting furnace together with air, etc., so that the carbonaceous material reacts with oxygen to generate combustible gas, and the charged raw material is melted by the heat of this reaction. Next, the discharged high temperature combustible gas is introduced into the primary raw material preheater,
Sensible heat is recovered by preheating the raw material charged in this chamber, and the high-temperature exhaust gas obtained by burning the combustible exhaust gas after the sensible heat recovery is introduced into the secondary raw material preheater. Since the heat is recovered by preheating other raw materials charged at high temperature, there is no need to perform arc heating throughout the entire process, and even if it is used, it is only used during the initial molten steel production, significantly reducing power consumption. can be reduced to
具体的には、従来において、溶解炉の大きさに
もよるが原料溶解のために電力エネルギ450〜
470KWH/Tを必要とし、オイルバーナ等の助
燃エネルギ等を利用しても360〜400KWH/Tを
必要としたが、本発明方法によれば250KWH/
T以下にでき、大幅な省電力化を図ることができ
る。 Specifically, in the past, depending on the size of the melting furnace, the electric energy used to melt raw materials was 450 ~
470KWH/T was required, and even if auxiliary combustion energy such as an oil burner was used, 360 to 400KWH/T was required, but according to the method of the present invention, 250KWH/T was required.
T or less, and significant power savings can be achieved.
また、原料溶解時に発生する高温可燃ガスか
ら、顕熱回収と潛熱回収とを行なつて2段階回収
をなしているので、従来では30〜50KWH/Tの
熱回収量であつたが、本発明方法では70〜
100KWH/Tに熱回収量を向上させることがで
きる。 In addition, since the high-temperature combustible gas generated when melting raw materials is recovered in two stages by performing sensible heat recovery and infrared heat recovery, the amount of heat recovered was conventionally 30 to 50 KWH/T, but the present invention 70~
The amount of heat recovery can be improved to 100KWH/T.
更には、1次原料予熱器2及び2次原料予熱器
4において、それぞれ低温予熱及び高温予熱がで
きるので予熱すべき原料の種類により、低温予熱
をすべきか高温予熱をすべきかを選択することが
でき予熱状態の選択の自由度を増すことができ
る。すなわち、原料の種類により溶融温度が異な
ることから、原料の溶融温度が低い場合には予熱
時における原料溶融を抑制するために低温予熱を
行ない、原料を溶融温度が高い場合には高温予熱
を行なうようにする。 Furthermore, since the primary raw material preheater 2 and the secondary raw material preheater 4 can perform low-temperature preheating and high-temperature preheating, respectively, it is possible to select whether low-temperature preheating or high-temperature preheating should be performed depending on the type of raw material to be preheated. The degree of freedom in selecting preheating conditions can be increased. That is, since the melting temperature differs depending on the type of raw material, if the melting temperature of the raw material is low, low-temperature preheating is performed to suppress raw material melting during preheating, and if the raw material has a high melting temperature, high-temperature preheating is performed. Do it like this.
[発明の効果]
以上要するに、本発明によれば次のような優れ
た効果を発揮することができる。[Effects of the Invention] In summary, according to the present invention, the following excellent effects can be achieved.
(1) 炭材吹込により可燃ガス生成反応をさせて、
この反応熱により原料を溶解し、得られる高温
可燃ガスから顕熱及び潛熱を回収するようにし
たので、従来例に比較して消費電力を大幅に削
減することができる。(1) A combustible gas generation reaction is caused by injecting carbonaceous material,
Since the raw material is melted by this reaction heat and sensible heat and heat are recovered from the resulting high-temperature combustible gas, power consumption can be significantly reduced compared to the conventional example.
(2) 低温予熱時に発生する悪臭成分を、燃焼塔内
における可燃ガスの燃焼時に発生する高温ガス
により熱分解できるので悪臭公害を防止するこ
とができる。(2) Malodorous components generated during low-temperature preheating can be thermally decomposed by high-temperature gas generated during combustion of combustible gas in the combustion tower, thereby preventing malodor pollution.
(3) 低温予熱と高温予熱とができるので、原料の
種類により予熱状態を選択することができ、予
熱状態選択の自由度を増すことができる。(3) Since low-temperature preheating and high-temperature preheating are possible, the preheating state can be selected depending on the type of raw material, and the degree of freedom in selecting the preheating state can be increased.
第1図は本発明方法を実施するための溶解炉設
備を示す概略平面図である。
尚、図中、1は溶解炉、2は1次原料予熱器、
3は燃焼塔、4は2次原料予熱器、9は炭材吹込
口、19は燃焼用空気予熱器である。
FIG. 1 is a schematic plan view showing melting furnace equipment for carrying out the method of the present invention. In addition, in the figure, 1 is a melting furnace, 2 is a primary raw material preheater,
3 is a combustion tower, 4 is a secondary raw material preheater, 9 is a carbon material inlet, and 19 is a combustion air preheater.
Claims (1)
を酸素含有気体の存在下で可燃ガス生成反応させ
てこの反応熱により原料を溶解し、得られる高温
可燃ガスにより他の原料を予熱して顕熱を回収
し、次いで、顕熱回収後の可燃ガスを燃焼させて
発生する高温排ガスにより更に他の原料を予熱し
て潛熱を回収するようにしたことを特徴とするス
クラツプ等の溶解方法。1. When melting raw materials such as scrap, carbonaceous materials undergo a reaction to generate combustible gas in the presence of oxygen-containing gas, the raw material is melted by the heat of reaction, and the resulting high-temperature combustible gas is used to preheat other raw materials to generate sensible heat. A method for melting scrap, etc., characterized in that the combustible gas after sensible heat recovery is burned, and then other raw materials are preheated using the high temperature exhaust gas generated to recover the heat.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP25405484A JPS61134586A (en) | 1984-12-03 | 1984-12-03 | Method of melting scrap, etc. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP25405484A JPS61134586A (en) | 1984-12-03 | 1984-12-03 | Method of melting scrap, etc. |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61134586A JPS61134586A (en) | 1986-06-21 |
| JPH0535349B2 true JPH0535349B2 (en) | 1993-05-26 |
Family
ID=17259587
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP25405484A Granted JPS61134586A (en) | 1984-12-03 | 1984-12-03 | Method of melting scrap, etc. |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS61134586A (en) |
-
1984
- 1984-12-03 JP JP25405484A patent/JPS61134586A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS61134586A (en) | 1986-06-21 |
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