JPS6065752A - Raw material powder calcining process - Google Patents
Raw material powder calcining processInfo
- Publication number
- JPS6065752A JPS6065752A JP13602584A JP13602584A JPS6065752A JP S6065752 A JPS6065752 A JP S6065752A JP 13602584 A JP13602584 A JP 13602584A JP 13602584 A JP13602584 A JP 13602584A JP S6065752 A JPS6065752 A JP S6065752A
- Authority
- JP
- Japan
- Prior art keywords
- raw material
- combustion
- material powder
- combustion chamber
- calciner
- 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
Links
- 239000002994 raw material Substances 0.000 title claims description 82
- 239000000843 powder Substances 0.000 title claims description 52
- 238000001354 calcination Methods 0.000 title claims description 47
- 238000000034 method Methods 0.000 title claims description 13
- 238000002485 combustion reaction Methods 0.000 claims description 107
- 239000000446 fuel Substances 0.000 claims description 39
- 238000002156 mixing Methods 0.000 claims description 30
- 238000000926 separation method Methods 0.000 claims description 14
- 238000011144 upstream manufacturing Methods 0.000 claims description 3
- 239000000567 combustion gas Substances 0.000 description 14
- 238000006243 chemical reaction Methods 0.000 description 13
- 239000007789 gas Substances 0.000 description 11
- 238000010304 firing Methods 0.000 description 9
- 238000010586 diagram Methods 0.000 description 6
- 239000004449 solid propellant Substances 0.000 description 6
- MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- 239000004568 cement Substances 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 239000003245 coal Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- JTJMJGYZQZDUJJ-UHFFFAOYSA-N phencyclidine Chemical class C1CCCCN1C1(C=2C=CC=CC=2)CCCCC1 JTJMJGYZQZDUJJ-UHFFFAOYSA-N 0.000 description 2
- 230000001133 acceleration Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920002577 polybenzoxazole Polymers 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
Landscapes
- Curing Cements, Concrete, And Artificial Stone (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
本発明は原料予熱装置と焼成炉との間に配置されたセメ
ント原料等原料粉末の仮焼方法に関し、殊に仮焼炉内で
の燃料の燃焼性を向上させると同時に燃焼ガスから原料
粉末への熱伝達と原料粉末の仮焼反応を促進し、以って
燃料消費量の低減或いは設備の小型化を達成可能とし、
更に仮焼炉内でのNoX 、(窒素酸化物)の発生を抑
制することのできる殊に固体燃料や低品位燃料の使用に
適した原料粉末の仮焼方法を提供するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for calcination of raw material powder such as cement raw material disposed between a raw material preheating device and a kiln, and particularly to a method for calcination of raw material powder such as a cement raw material disposed between a raw material preheating device and a kiln. At the same time, it promotes heat transfer from combustion gas to raw material powder and calcination reaction of raw material powder, thereby reducing fuel consumption or downsizing equipment.
Furthermore, the present invention provides a method for calcination of raw material powder, which is particularly suitable for use with solid fuels and low-grade fuels, and is capable of suppressing the generation of NoX (nitrogen oxides) in a calcination furnace.
近代的上メント焼成装置は原料粉末の流れの方向に見て
原料予熱装置と焼成炉との間に独立した熱源を有する仮
焼炉を配置して構成される。A modern calcining apparatus is constructed by disposing a calcining furnace having an independent heat source between the raw material preheating device and the calcining furnace when viewed in the direction of flow of the raw material powder.
第1図は、セメント原料粉末を予熱・仮焼・焼成・冷却
する工程を示す線図的系統図で、図中の実線矢印は熱風
の流れ、破線矢印は原料粉末の流れを示す。尚装置の概
要は、ザイクロン等の原料粉末分離器Cl−03および
ダクト7等より構成される原料予熱装置11分離サイク
ロンC1を付属する仮焼炉2.ロータリキルン等の焼成
炉i及びクリンカ冷却機4から成り、原料投入シュート
5から供給されたセメント原料粉末は、第1〜第3の各
サイクロンC,−wc3を順次降下し、他方焼成炉3及
び仮焼炉2からの高温排ガスは誘引通風機8により吸引
されて原料予熱装置1内を上昇するから、ダクト7内及
びサイクロンC,−C3内にて原料粉末と高温ガスとの
混合・熱交換・分離が繰り返される。予熱された原料粉
末は原料予熱装置1から予熱原料シュート14を通して
仮焼炉2へ導入される。他方、クリンカ冷却機4がら抽
気ダクト13を通して仮焼炉2へ導入される高温の燃焼
用2次空気と、バーナ6aから燃焼用1次空気と共に供
給される燃料によって仮焼炉2内で燃焼が起こり、その
燃焼熱と焼成炉排ガスのもつ熱を受けることにより原料
粉末が仮焼される。FIG. 1 is a diagrammatic system diagram showing the steps of preheating, calcining, firing, and cooling cement raw material powder, and the solid arrows in the figure indicate the flow of hot air, and the dashed arrows indicate the flow of the raw material powder. The outline of the apparatus is as follows: 11 a raw material preheating device consisting of a raw material powder separator Cl-03 such as Zylon, a duct 7, etc., a calcining furnace 2. It consists of a kiln i such as a rotary kiln and a clinker cooler 4, and the cement raw material powder supplied from the raw material input chute 5 descends sequentially through the first to third cyclones C and -wc3, and the other kiln 3 and clinker cooler 4. The high-temperature exhaust gas from the calcining furnace 2 is sucked by the induced draft fan 8 and rises inside the raw material preheating device 1, so that the raw material powder and the high-temperature gas are mixed and heat exchanged in the duct 7 and the cyclones C and -C3.・Separation is repeated. The preheated raw material powder is introduced from the raw material preheating device 1 into the calciner 2 through the preheated raw material chute 14. On the other hand, combustion is carried out in the calciner 2 by the high temperature secondary combustion air introduced from the clinker cooler 4 into the calciner 2 through the bleed air duct 13 and the fuel supplied from the burner 6a together with the primary combustion air. The raw material powder is calcined by receiving the combustion heat and the heat of the firing furnace exhaust gas.
仮焼された原料粉末は燃焼ガスと共に仮焼炉2から分離
手段としての分離サイクロンC4に入って燃焼ガスから
分離されたのち、仮焼原料シュート15より焼成炉人口
端口12を通して焼成炉3に入り、焼成炉3の下端側に
設置したバーナ6bから供給される燃料の燃焼熱により
焼成炉3内で必要な熱処理を受けてクリンカになったの
ち、冷却fi4で冷却される。尚、クリンカ冷却用の空
気は押込送風taloによって供給され、クリンカと熱
交換を行って昇温した空気の一部は、上述の如く仮焼炉
2及び焼成炉3に分配導入されるが、余剰の空気は誘引
通風機9により排出される。そしてクリンカ冷却機4か
ら出たクリンカはコンヘア11によって次工程へ搬出さ
れる。The calcined raw material powder enters the separation cyclone C4 as a separation means from the calciner 2 together with the combustion gas and is separated from the combustion gas, and then enters the calciner 3 from the calciner raw material chute 15 through the calciner port 12. After being subjected to necessary heat treatment in the firing furnace 3 by the combustion heat of fuel supplied from the burner 6b installed at the lower end of the firing furnace 3 to become clinker, it is cooled by cooling fi4. Note that the air for clinker cooling is supplied by forced air blowing talo, and a part of the air that has been heated by exchanging heat with the clinker is distributed and introduced into the calcining furnace 2 and the calcining furnace 3 as described above. The air is exhausted by the induced draft fan 9. The clinker discharged from the clinker cooler 4 is transported to the next process by a conhair 11.
第2図は第1図におりる仮焼炉付近の構成をより詳細に
示す概念図で、これらの図により仮焼炉の構造及び機能
を説明すると下記の通りである。FIG. 2 is a conceptual diagram showing in more detail the structure around the calcining furnace shown in FIG. 1, and the structure and function of the calcining furnace will be explained with reference to these figures as follows.
即ち、仮焼炉2は本構成例では円筒状竪形で、絞り部2
cを境にして互いに連通した燃焼帯を形成する上流側(
下方)の燃焼室2aと混合帯を形成する下流側(上方)
の混合室2しとで構成され、燃焼室2aの下端は下方に
向けて漸次断面を縮小して逆円錐体状部とし、開口2Δ
により入口端ff112を介して焼成炉3に接続してい
る。又、燃焼室2&の下部側壁には半径方向または接線
方向にクリンカ冷却1illI4からの高温抽気を燃焼
用2次空気として案内する抽気ダクト13が開口2eに
て接続され、当該抽気ダクト13の天井壁が燃焼室2@
側壁と接合する付近には、燃焼室2aに流入する高温抽
気に指向して、1次空気と共に燃料を吹込むバーナ6、
を設置し、更に当該バーナ6aの上方に位置し、バーナ
6aから供給される燃料により燃焼室2つ内に形成され
る燃焼域を指向して原料予熱袋W1のサイクロンC3か
らの予熱原料投入シュート14が接続され、一方混合室
2I。That is, in this configuration example, the calcining furnace 2 has a cylindrical vertical shape, and the constricted part 2
The upstream side (
The downstream side (upper side) forming a mixing zone with the combustion chamber 2a (lower side)
The lower end of the combustion chamber 2a has an inverted conical shape with its cross section gradually reduced downward, and an opening 2Δ
It is connected to the firing furnace 3 via the inlet end ff112. Further, a bleed air duct 13 that guides high-temperature bleed air from the clinker cooling 1illI4 as secondary air for combustion is connected to the lower side wall of the combustion chamber 2& in the radial or tangential direction through an opening 2e, and the ceiling wall of the bleed air duct 13 is combustion chamber 2@
A burner 6, which blows fuel together with primary air toward the high-temperature bleed air flowing into the combustion chamber 2a, is located near the side wall.
and a preheated raw material input chute from the cyclone C3 of the raw material preheating bag W1, which is located above the burner 6a and is directed toward the combustion zone formed in the two combustion chambers by the fuel supplied from the burner 6a. 14 is connected, while mixing chamber 2I.
の燃焼ガス出口2fは分離サイクロンC4に接続されて
いる。The combustion gas outlet 2f of is connected to the separation cyclone C4.
これらの装置を用いるに当たって、原料予熱装置1から
の予熱原料はシュート14を通して仮焼炉2の燃焼帯を
形成する燃焼室2□内に供給され、入目端覆12を介し
て開口2aを通して下方より上昇流入する焼成炉3から
の排ガスにより燃焼室28内にて混合・攪拌され、噴流
層を形成している。該噴tL層内には抽気ダクト13を
通してクリンカ冷却機4からの高温抽気が燃焼用2次空
気として導入され、当該抽気ダクト13の燃焼室2aへ
の導入口2e上方に設置されたバーナ6fiを通して燃
焼用1次空気と共に燃料が供給され、噴流層内にて燃焼
が行われる。予熱原料シュート14を通して燃焼室2.
内に供給された原料粉末はこれら燃料の燃焼熱および焼
成炉排ガスの1Ili熱を吸収して仮焼反応を進行させ
つつ燃焼ガスと共に絞り部2Cを通過して混合帯を形成
する混合室2bに導入されるが、絞り部2Cを通過する
際の加速および減速による拡散す」果と混合室2し内に
発生する乱流により攪拌・混合が促進され、混合室2し
内にて燃焼ガス中に含まれる可燃成分の完全燃焼を行っ
たのち、開口2fより分離手段を構成する分離サイクロ
ンC+に排出するようになっている。When using these devices, the preheated raw material from the raw material preheating device 1 is supplied through the chute 14 into the combustion chamber 2 □ that forms the combustion zone of the calciner 2, and is passed through the opening 2a through the entrance end cover 12 and downwardly. The exhaust gases from the firing furnace 3 flowing upward are mixed and stirred in the combustion chamber 28 to form a spouted bed. The high-temperature bleed air from the clinker cooler 4 is introduced into the jet tL layer through the bleed air duct 13 as secondary air for combustion, and through the burner 6fi installed above the inlet 2e of the bleed air duct 13 into the combustion chamber 2a. Fuel is supplied together with primary air for combustion, and combustion occurs within the spouted bed. The combustion chamber 2 through the preheated feed chute 14.
The raw material powder supplied into the chamber absorbs the combustion heat of the fuel and the heat of the firing furnace exhaust gas to advance the calcination reaction, and passes through the throttle part 2C together with the combustion gas to the mixing chamber 2b forming a mixing zone. However, the agitation and mixing is promoted by the diffusion effect due to acceleration and deceleration when passing through the constriction part 2C and the turbulent flow generated in the mixing chamber 2, and the combustion gas is mixed inside the mixing chamber 2. After complete combustion of the combustible components contained in the fuel, the fuel is discharged from the opening 2f to the separation cyclone C+ that constitutes the separation means.
この様な噴流層式仮焼炉或いは気流式仮焼炉の燃焼室2
aにおいては、原料予熱装置からの仮焼すべき予熱原料
の全量が燃焼室に直接供給されるか或いは燃焼室を通過
するようになっており、燃焼室内での燃料の燃焼による
発生熱が直ちに原料粉末に伝達されるため、仮焼炉燃焼
室内の温度は燃焼室での熱収支から決定される平衡温度
に近くなっており、バーナ装着部の近傍を除いて900
℃前後の比較的低温に維持されている。Combustion chamber 2 of such a spouted bed type calciner or air flow type calciner
In a, the entire amount of the preheated raw material to be calcined from the raw material preheating device is directly supplied to the combustion chamber or passes through the combustion chamber, and the heat generated by the combustion of the fuel in the combustion chamber is immediately absorbed. Because the temperature is transmitted to the raw material powder, the temperature inside the calciner combustion chamber is close to the equilibrium temperature determined from the heat balance in the combustion chamber.
It is maintained at a relatively low temperature around ℃.
この様に仮焼炉燃焼室内が低温に維持されていることは
燃焼室2aの炉壁を十分安全に保護するためには有効で
あるが、燃焼室2a内での燃料の燃焼性を阻害しており
、仮焼炉2全体として中間絞り機構2cとこれに後続す
る混合室2トを設けて燃料燃焼性の向上をはかってはい
るものの、十分な燃焼を確保するためには理論的に必要
な燃焼空気量よりも相当過剰の燃焼空気を仮焼炉へ導入
する必要があり、仮焼炉での燃料消費量の増大を招いて
いる。殊に、仮焼用燃料として微粉炭等の固体燃料を使
用したり或いは低品位燃料を使用する場合には、重油等
の液体燃料に比べて燃焼時間が長くかかるため、燃料の
燃焼室内滞留時間の延長を目的として燃焼室容量を大き
く採る必要があり、設備費の増大を招いている。Maintaining the inside of the calciner combustion chamber at a low temperature in this way is effective in sufficiently safely protecting the furnace wall of the combustion chamber 2a, but it also inhibits the combustibility of the fuel within the combustion chamber 2a. Although the calciner 2 as a whole is equipped with an intermediate throttle mechanism 2c and a mixing chamber 2c following it to improve fuel combustibility, it is theoretically necessary to ensure sufficient combustion. It is necessary to introduce a considerable amount of combustion air into the calciner in excess of the amount of combustion air required, leading to an increase in fuel consumption in the calciner. In particular, when solid fuel such as pulverized coal or low-grade fuel is used as the calcining fuel, the combustion time is longer than that of liquid fuel such as heavy oil, so the residence time of the fuel in the combustion chamber is In order to extend the combustion chamber, it is necessary to increase the capacity of the combustion chamber, leading to an increase in equipment costs.
又、仮焼炉内での原料粉末の仮焼反応の進行度合は雰囲
気ガス中の炭酸ガス分圧にも関係するが、主として雰囲
気ガス温度に支配されるため燃焼室内が低温に維持され
る場合には原料粉末粒子の中心部まで充分に仮焼反応を
進行させることができないので、仮焼炉から焼成炉へ排
出する原料粉末の仮焼率も充分満足できるに至っていな
い。更に、仮焼炉での燃焼は燃料中に含まれる窒素分に
起因する所謂フューエルNoXのもっとも発生しやすい
温度領域で行われるため、特に燃料として窒素含有量の
多い微粉炭等の固体燃料を使用する場合には仮焼炉内で
大量のNo、を発生し、原料予熱装置からこれを排出し
て大気を汚染する原因となっている。In addition, the degree of progress of the calcination reaction of the raw material powder in the calcination furnace is related to the partial pressure of carbon dioxide in the atmospheric gas, but it is mainly controlled by the temperature of the atmospheric gas, so if the inside of the combustion chamber is maintained at a low temperature. Since the calcination reaction cannot sufficiently proceed to the center of the raw material powder particles, the calcination rate of the raw material powder discharged from the calcination furnace to the calcination furnace has not been sufficiently satisfied. Furthermore, since combustion in a calciner is carried out in the temperature range where so-called fuel No In this case, a large amount of NO is generated in the calcining furnace, which is discharged from the raw material preheating device, causing atmospheric pollution.
本発明は従来技術のもつ上記問題点を解消し、仮焼炉燃
焼室内の雰囲気温度を適度な高温に調節・維持すること
により、燃料の燃焼性を向上させ、燃焼用過剰空気量の
低減と原料粉末仮焼反応の促進により燃料消q!!量を
節減し或いは設備の小型化を達成し、同時に仮焼炉内で
のNOxの発生を効果的に抑制できるようにした原料粉
末の仮焼方法を提供しようとするものである。The present invention solves the above-mentioned problems of the prior art, improves the combustibility of fuel, and reduces the amount of excess air for combustion by adjusting and maintaining the atmospheric temperature inside the calciner combustion chamber at an appropriately high temperature. Fuel consumption is reduced by promoting the calcining reaction of raw material powder! ! The object of the present invention is to provide a method for calcining raw material powder that can reduce the amount of raw material powder or downsize the equipment, and at the same time can effectively suppress the generation of NOx in the calciner.
以下図面に基づいて本発明の詳細な説明するが、図は具
体的な実施の一例を示すもので、本発明はこれらの図示
例に限定されず、前・後記の趣旨に沿って他の構成とし
たり、或いは一部の段組を変更しても同様に実施するこ
とができる。The present invention will be described in detail below based on the drawings, but the drawings show specific examples of implementation, and the present invention is not limited to these illustrated examples. Alternatively, the same implementation can be performed by changing some of the columns.
第3図は本発明の一実施例を示す概念図であり、仮焼炉
2本体の基本的構造、仮焼炉2への焼成炉3からの排ガ
ス導入方法、抽気ダクト13からの高温燃焼用2次空気
の導入方法、仮焼炉2内の燃焼ガスの流れおよび仮焼炉
2からの燃焼ガスの排出方法などについては前述の第2
図での従来装置の場合と同様である。FIG. 3 is a conceptual diagram showing one embodiment of the present invention, showing the basic structure of the main body of the calciner 2, the method of introducing exhaust gas from the calciner 3 into the calciner 2, and the method for high-temperature combustion from the extraction duct 13. Regarding the method of introducing secondary air, the flow of combustion gas in the calciner 2, the method of discharging the combustion gas from the calciner 2, etc., please refer to the above-mentioned Section 2.
This is the same as the case of the conventional device shown in the figure.
そこで第3図に基づいて、第2図との相違点として本発
明の構成を詳細に説明すると、原料予熱装置のザイクロ
ンC3からの予熱原料シュート14は取付角度を調整可
能な分配弁14cを備えた分岐部材14Jにより2本の
予熱原料シュート14a、14bに分岐され、一方の分
離シュート148は仮焼炉2の燃焼帯を形成する燃焼室
2aに、又他方の分岐シュート14I、は仮焼炉2の混
合帯を形成する混合室21.に接続される。これら分岐
シュート14.Iおよび14bと燃焼室2aおよび混合
室2しとの接続位Wについては特に限定されないが、就
中分岐シュート14.lにより燃焼室2aに投入する予
熱原料粉末はバーナ6aにより燃焼室2□内に形成され
る燃焼域を指向させて燃焼室り内に局部的高温部が形成
されるのを防止するか、或いは仮焼炉2の下端開口2a
より燃焼室2a内に上昇・流入する焼成炉3からの排ガ
スに指向させて燃焼室2a内により濃密な第1の噴流)
弓を形成するのを助成し、又分岐シューl141゜によ
り混合室2t、に投入する予熱原料わ)末は仮焼炉2の
中間絞り部2cから混合室2b内に上昇・流入する燃焼
室2aからの燃焼ガスに指向させて混合室2I、内に第
2の噴流層を形成するのを助成するような接続配置が推
奨される。Therefore, based on FIG. 3, the configuration of the present invention will be explained in detail as a difference from FIG. The branching member 14J branches the preheated material into two chutes 14a and 14b, one separation chute 148 is connected to the combustion chamber 2a forming the combustion zone of the calciner 2, and the other branch chute 14I is connected to the combustion chamber 2a forming the combustion zone of the calciner 2. 2 mixing chambers 21. connected to. These branching chutes14. The connection point W between the combustion chamber 2a and the mixing chamber 2 and the combustion chamber 2a and the mixing chamber 2 is not particularly limited; The preheated raw material powder introduced into the combustion chamber 2a by the burner 6a is directed to the combustion zone formed in the combustion chamber 2□ to prevent the formation of localized high temperature areas in the combustion chamber, or Lower end opening 2a of calcining furnace 2
(The first jet stream is directed toward the exhaust gas from the firing furnace 3 that rises and flows into the combustion chamber 2a, making it more dense inside the combustion chamber 2a)
The preheated raw material which assists in forming the bow and is fed into the mixing chamber 2t by the branch shoe l141°) is the combustion chamber 2a which rises and flows into the mixing chamber 2b from the intermediate constriction part 2c of the calciner 2. A connection arrangement is recommended that helps direct the combustion gases from the mixing chamber 2I to form a second spouted bed.
この様な構成により、燃焼室2aには原料予熱装置から
の仮焼すべき予熱原料の一部が供給されるだけであり、
混合室2bに供給した予熱原料は実質的に燃焼室28を
1ffl過することなく分離サイクロンC1へ導入され
るため、従来構造による場合に較べて燃焼室21内の温
度を高めることができる。この燃焼室2.内の温度は燃
焼室2aと混合室2bとへの予熱原料の分配割合によっ
て8)!a整され、次に述べる燃料の燃焼性、No、の
発生。With such a configuration, only a part of the preheated raw material to be calcined from the raw material preheating device is supplied to the combustion chamber 2a,
Since the preheated raw material supplied to the mixing chamber 2b is introduced into the separation cyclone C1 without substantially passing through the combustion chamber 28 by 1 ffl, the temperature inside the combustion chamber 21 can be increased compared to the case of the conventional structure. This combustion chamber 2. The temperature inside depends on the distribution ratio of the preheated raw material to the combustion chamber 2a and the mixing chamber 2b (8)! a, and the combustibility of the fuel, which will be described next, occurs.
炉壁への原料コーチングの生成および炉壁の熱的保護等
を総合的に勘案して選定されるが、一般に950〜11
00℃、このましくは1000〜1050℃の高温雰囲
気とするのが適当であり、このためには原料予熱装置か
らの予熱原料の90〜50%を燃焼室21へ、又その残
りの10〜50%を混合室2しへ分配・供給する。ここ
に燃焼室2□内での燃焼温度の効果につき説明すると、
まず燃料の燃焼速度は燃焼室28内絶対温度の指数関数
的に著しく大となるため僅かの過剰空気で充分な燃焼を
行うことができるようになり、又燃焼ガスと供給原料と
の大きな温度差にもとづき燃料の燃焼熱を有効かつ速や
かに原料粉末へ伝達することができる様になるので仮焼
炉での燃料滴η’fflを低減させることができる。又
、微粉炭等の固体燃料或いは低品位燃料を使用する場合
にも燃焼温度の上昇により必要燃焼時間が短縮されるの
で、仮焼炉の容禎を小さく選定することができる。更に
、燃焼室2a内温度は同室内燃焼ガス中の炭酸ガス分圧
により決定される原ネ1粉末の仮焼反応温度よりも道か
に高くなるので、分岐シュー+−14゜より燃焼室2.
に供給した原料15)末は燃焼室2a内にて速やかに仮
焼反応を完了するようになる。It is selected by comprehensively considering the formation of raw material coating on the furnace wall and the thermal protection of the furnace wall, but generally 950 to 11
It is appropriate to create a high-temperature atmosphere of 00°C, preferably 1000-1050°C, and for this purpose, 90-50% of the preheated raw material from the raw material preheating device is sent to the combustion chamber 21, and the remaining 10-50% is Distribute and feed 50% to mixing chamber 2. Here, we will explain the effect of combustion temperature in combustion chamber 2□.
First, the combustion rate of the fuel increases exponentially with the absolute temperature inside the combustion chamber 28, so sufficient combustion can be achieved with a small amount of excess air, and the large temperature difference between the combustion gas and the feed material Based on this, the combustion heat of the fuel can be effectively and quickly transferred to the raw material powder, so that the fuel droplets η'ffl in the calciner can be reduced. Furthermore, even when solid fuel such as pulverized coal or low-grade fuel is used, the required combustion time is shortened due to the increase in combustion temperature, so the capacity of the calciner can be selected to be small. Furthermore, since the temperature inside the combustion chamber 2a is much higher than the calcination reaction temperature of the raw material 1 powder, which is determined by the partial pressure of carbon dioxide in the combustion gas in the same chamber, the combustion chamber 2 ..
The raw material 15) powder supplied to the combustion chamber 2a quickly completes the calcination reaction.
一方分岐シュー114bより混合室2トに供給した原ネ
」粉末は従来技術と同程度に仮焼反応を進行させること
ができ、又混合室2bに供給する原料粉末量は燃焼室2
aへ供給し仮焼反応が著しく進行した原料粉末よりも少
量であるので、これらの混合原料として分離サイクロン
C,から焼成炉3へ排出する仮焼原料粉末は従来技術と
同程度の温度であるにも拘らず仮焼反応がより一層進行
した状態となっており、焼成装置全体としての熱効率を
向上させることができる。次に燃焼室2a内でのNOx
の発生につき説明すると、公知の如(NOxには大別し
て燃料中の窒素分に起因するフューエルNOxと燃焼空
気中の窒素分に起因するサーマルNOxとがあり、一般
に)j!、 −= :f−JL/ N Oxは約900
℃を越えた温度領域では高温になるほど発生量が減少し
、サーマルNOxは1100〜1200℃程度の燃焼域
温度を越えると徐々に増加し、共に燃焼域酸素濃度が高
くなる程発生量も増加する。本発明装置によれば、燃焼
域温度がフューエルNOxとサーマルNO8との両方が
発生しにくい温度領域になっており、しかも前述の如く
燃焼域内の過剰空気の減少によって酸素濃度を低く維持
することができるのでNOxの発生を著しく抑制するこ
とができる。この際、燃焼室内温度が1100℃程度を
越える場合には燃焼室2aの壁面に原料粉末のコーチン
グを発生しやすくなり、又炉壁の熱的保護の面からも燃
焼室内温度をこの程度に抑えることが望ましく、更に燃
焼室内温度が950℃程度より低い場合には燃料の燃焼
什、げ斜rA史の悔焼性ルびNO,の抑制の面で改善効
果が少ない。面、仮焼炉2の中間絞り都2c付近におけ
る燃焼ガス温度とNOx含有量を測定し、これにより分
配弁14cを調整することにより燃焼性との兼合いにお
いてNOx発生量を容易に制御することができ、操業条
件が変動しても常に安定して低く抑制することが可能と
なる。On the other hand, the raw powder supplied to the mixing chamber 2 through the branch shoe 114b can undergo a calcination reaction to the same extent as in the prior art, and the amount of raw powder supplied to the mixing chamber 2b is
Since the amount is smaller than the raw material powder supplied to a and where the calcination reaction has significantly progressed, the temperature of the calcination raw material powder discharged from the separation cyclone C to the firing furnace 3 as a mixed raw material is about the same as that of the conventional technology. Despite this, the calcination reaction has progressed further, and the thermal efficiency of the calcination apparatus as a whole can be improved. Next, NOx inside the combustion chamber 2a
To explain the generation of NOx, as is known (in general, there are two types of NOx: fuel NOx, which is caused by the nitrogen content in the fuel, and thermal NOx, which is caused by the nitrogen content in the combustion air). , -= :f-JL/N Ox is approximately 900
In the temperature range above ℃, the amount generated decreases as the temperature increases, and thermal NOx gradually increases when the combustion zone temperature exceeds about 1100 to 1200℃, and the amount generated increases as the combustion zone oxygen concentration increases. . According to the device of the present invention, the temperature of the combustion zone is in a temperature range in which both fuel NOx and thermal NO8 are difficult to generate, and as described above, the oxygen concentration can be maintained low by reducing excess air in the combustion zone. Therefore, the generation of NOx can be significantly suppressed. At this time, if the temperature in the combustion chamber exceeds about 1100°C, coating of raw material powder is likely to occur on the wall surface of the combustion chamber 2a, and from the standpoint of thermal protection of the furnace wall, the temperature in the combustion chamber should be kept to this level. Further, if the temperature inside the combustion chamber is lower than about 950° C., there is little improvement effect in terms of suppressing the combustion of the fuel and the retardation of the combustion history. To easily control the amount of NOx generated in consideration of combustibility by measuring the combustion gas temperature and NOx content near the intermediate throttle cap 2c of the calciner 2 and adjusting the distribution valve 14c accordingly. This makes it possible to always maintain a stable low level even when operating conditions fluctuate.
この様に燃焼室2a内の高いぢ;囲気温度にもとづき、
NOxの発生を抑制しつつも燃料のMARと原料粉末の
仮焼反応とが共に高度に進行した状態で、燃焼ガスおよ
び原料粉末は絞り部2cを通過して混合室2I、に導入
され、分岐シューl−’14bを通して供給される予熱
原t4わ)末の1部と攪拌・混合され、ここに第2の噴
流j何を形成して原料粉末を滞溜させ、新たに供給され
た原料粉末の仮焼反応を進行させて900℃前後に温度
降下した低温雰囲気となり、混合室2I、の関口2萱よ
り分離サイクロンC,へ排出される。この際、中間絞り
部2cを通過する」二昇ガスは増速されているので、分
岐シュート14bを通して混合室2I、に供給された原
料粉末の実質的な部分が燃焼室2nへ落下するのが防止
され、燃焼室2□内を高温に維持することができる。In this way, the temperature inside the combustion chamber 2a is high; based on the surrounding air temperature,
In a state where both the MAR of the fuel and the calcining reaction of the raw material powder are highly advanced while suppressing the generation of NOx, the combustion gas and the raw material powder pass through the throttle part 2c and are introduced into the mixing chamber 2I, where they are branched. It is stirred and mixed with a part of the preheated raw material t4) supplied through the shoe 14b, and a second jet is formed here to stagnate the raw material powder, and the newly supplied raw material powder As the calcination reaction progresses, a low-temperature atmosphere is created in which the temperature drops to around 900°C, and the mixture is discharged from Sekiguchi 2 of mixing chamber 2I to separation cyclone C. At this time, since the "secondary gas" passing through the intermediate constriction part 2c is accelerated, a substantial portion of the raw material powder supplied to the mixing chamber 2I through the branch chute 14b falls into the combustion chamber 2n. This is prevented, and the inside of the combustion chamber 2□ can be maintained at a high temperature.
これらの仮焼炉構造におい°C1仮焼炉断面の形状およ
び燃料や燃焼用空気の導入形態或いは仮焼炉への焼成炉
排ガスの導入の有無などは目的に応じて自由に選択でき
る。例えば、固体燃料を使用する場合にはバーナ6□に
替えて燃料供給シュートを配設し粉末状固体燃料を重力
により燃焼室2aへ落下・投入することもできる。又、
この際供給シュートを通して予熱原料粉末を固体燃料と
共に仮焼炉へ供給して燃焼室内の燃料供給部近傍に局部
的な高温域が形成されるのを防止したり、分離サイクロ
ンC4からの仮焼原料の一部を燃焼室に循環させたり、
或いは燃焼室2aの逆錐体状部に別個のバーナを設置す
るなど、NOx発生の抑制または脱硝に関する他の手段
と組み合わせることもできる。更には、原料予熱装置の
型式(サイクロン型、基型等)、系列数5段数、各段を
構成する粉末分離器の数等についても全く制限されない
。In these calciner structures, the shape of the °C1 calciner cross section, the introduction form of fuel and combustion air, and whether or not calciner exhaust gas is introduced into the calciner can be freely selected depending on the purpose. For example, when solid fuel is used, a fuel supply chute may be provided in place of the burner 6□, and the powdered solid fuel may fall and be introduced into the combustion chamber 2a by gravity. or,
At this time, the preheated raw material powder is supplied to the calciner together with the solid fuel through the supply chute to prevent the formation of a localized high temperature area near the fuel supply part in the combustion chamber, and the preheated raw material powder is supplied from the separation cyclone C4 to the calciner. Circulate part of the fuel into the combustion chamber,
Alternatively, it may be combined with other means for suppressing NOx generation or denitration, such as installing a separate burner in the inverted cone-shaped portion of the combustion chamber 2a. Furthermore, there are no restrictions at all regarding the type of raw material preheating device (cyclone type, base type, etc.), the number of five-stage series, the number of powder separators constituting each stage, etc.
本発明は以上の如く構成されており、原料予熱装置から
の予熱原料を仮焼炉に供給するに当り、仮焼炉を」−流
側の燃焼帯と下流側の混合帯とにより構成すると共に、
予熱原料をこれら燃焼帯と混合帯とに分割し且つ調整し
て供給することにより燃焼帯における雰囲気温度を適度
に高め、以って燃料の燃焼性を向上させ、燃焼ガスから
原料粉末への熱伝達と原料粉末の仮焼反応を促進し、燃
料消費量の低減と設備の小型化を達成し、尚且つ仮焼炉
内でのNOxの発生を著しく抑制することができるもの
である。The present invention is constructed as described above, and when supplying the preheated raw material from the raw material preheating device to the calciner, the calciner is configured with a combustion zone on the upstream side and a mixing zone on the downstream side. ,
By dividing the preheated raw material into the combustion zone and the mixing zone and supplying it in an adjusted manner, the atmospheric temperature in the combustion zone is appropriately raised, thereby improving the combustibility of the fuel, and reducing heat transfer from the combustion gas to the raw material powder. It promotes the transmission and calcination reaction of the raw material powder, reduces fuel consumption and downsizes the equipment, and can significantly suppress the generation of NOx in the calcination furnace.
第1図は従来の七メントタリン力製造工程を示す線図的
系統図、第2図は第1図における仮焼炉付近の概念図、
第3図は本発明の一実施例を示す概念図である。
(符号の説明)
■・・・原料予熱装W 2・・・仮焼炉2a・・・燃焼
室 2し・・・混合室
2、・・・絞り部 3・・・焼成炉
4・・・タリン力冷却機 6・・・燃料供給装置12・
・・入口端覆 13・・・抽気ダクト14・・・予熱原
料シュート
14m、14b・・・分岐シュート
14c・・・分配弁 14.l・・・分岐部材15・・
・仮焼原料シュート
c、−C3・・・原料粉末分離器
C4・・・分離サイクロン。
出願人 株式会社神戸M鋼所
代理人 弁理士 本庄 武男
第1図
τ
1
第2図Figure 1 is a diagrammatic system diagram showing the conventional 7-mentoring force production process, Figure 2 is a conceptual diagram of the vicinity of the calcining furnace in Figure 1,
FIG. 3 is a conceptual diagram showing an embodiment of the present invention. (Explanation of symbols) ■... Raw material preheating device W 2... Calcination furnace 2a... Combustion chamber 2... Mixing chamber 2,... Throttle section 3... Calcining furnace 4... Tallinn power cooler 6...Fuel supply device 12.
...Inlet end cover 13...Bleed air duct 14...Preheated raw material chute 14m, 14b...Branch chute 14c...Distribution valve 14. l... Branch member 15...
- Calcined raw material chute c, -C3... Raw material powder separator C4... Separation cyclone. Applicant Kobe M Steel Co., Ltd. Agent Patent Attorney Takeo Honjo Figure 1 τ 1 Figure 2
Claims (2)
の間に配設され、原料粉末の分離手段を付属した仮焼炉
が上流側の燃焼帯と下流側の混合帯とにより構成され、
該燃焼帯に燃料及び燃焼用空気を導入することにより燃
焼帯に供給した予熱原料粉末が混合帯を経て分離手段か
ら排出される間に仮焼するようにした原料粉末の仮焼方
法において、予熱原料粉末の50〜90%を燃焼帯に、
又10〜50%を混合帯に夫々供給すると共に、該混合
帯に供給した原料粉末の実質的な部分は燃焼帯を通過す
ることなく分離手段へ導入することにより、仮焼炉内の
前記燃焼帯を950〜1100℃の高温雰囲気とし、又
前記混合帯を900℃前後の低温雰囲気とすることを特
徴とする原料粉末の仮焼方法。(1) The calciner, which is disposed between the preheating device and the calcining furnace when viewed in the direction of flow of the raw powder, and is equipped with a means for separating the raw powder, separates the combustion zone on the upstream side and the mixing zone on the downstream side. configured,
In a method for calcining raw material powder, the preheated raw material powder supplied to the combustion zone is calcined while being discharged from the separation means via the mixing zone by introducing fuel and combustion air into the combustion zone. 50 to 90% of the raw material powder to the combustion zone,
In addition, 10 to 50% of the raw material powder is supplied to the mixing zone, and a substantial part of the raw material powder supplied to the mixing zone is introduced into the separation means without passing through the combustion zone, thereby reducing the combustion in the calciner. A method for calcination of raw material powder, characterized in that the zone is placed in a high temperature atmosphere of 950 to 1100C, and the mixing zone is placed in a low temperature atmosphere of around 900C.
することを特徴とする特許請求の範囲第1項に記載した
原料粉末の仮焼方法。(2) The method for calcining raw material powder as set forth in claim 1, characterized in that the combustion zone is set to a high temperature atmosphere of 1000 to 1050°C.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13602584A JPS6065752A (en) | 1984-06-29 | 1984-06-29 | Raw material powder calcining process |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13602584A JPS6065752A (en) | 1984-06-29 | 1984-06-29 | Raw material powder calcining process |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6065752A true JPS6065752A (en) | 1985-04-15 |
| JPH0152339B2 JPH0152339B2 (en) | 1989-11-08 |
Family
ID=15165423
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP13602584A Granted JPS6065752A (en) | 1984-06-29 | 1984-06-29 | Raw material powder calcining process |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6065752A (en) |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5429312A (en) * | 1977-08-09 | 1979-03-05 | Mitsubishi Metal Corp | Surface coated super hard alloy |
| JPS56100627A (en) * | 1980-01-17 | 1981-08-12 | Ishikawajima Harima Heavy Ind Co Ltd | Calcining method of powder raw material |
| JPS5895632A (en) * | 1981-12-03 | 1983-06-07 | 日本セメント株式会社 | Cement raw material coalcining furnace |
-
1984
- 1984-06-29 JP JP13602584A patent/JPS6065752A/en active Granted
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5429312A (en) * | 1977-08-09 | 1979-03-05 | Mitsubishi Metal Corp | Surface coated super hard alloy |
| JPS56100627A (en) * | 1980-01-17 | 1981-08-12 | Ishikawajima Harima Heavy Ind Co Ltd | Calcining method of powder raw material |
| JPS5895632A (en) * | 1981-12-03 | 1983-06-07 | 日本セメント株式会社 | Cement raw material coalcining furnace |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0152339B2 (en) | 1989-11-08 |
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