JPH0353265B2 - - Google Patents
Info
- Publication number
- JPH0353265B2 JPH0353265B2 JP26591884A JP26591884A JPH0353265B2 JP H0353265 B2 JPH0353265 B2 JP H0353265B2 JP 26591884 A JP26591884 A JP 26591884A JP 26591884 A JP26591884 A JP 26591884A JP H0353265 B2 JPH0353265 B2 JP H0353265B2
- Authority
- JP
- Japan
- Prior art keywords
- shaft
- quicklime
- combustion
- powdered
- firing
- 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
Links
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 claims description 112
- 239000000292 calcium oxide Substances 0.000 claims description 56
- 235000012255 calcium oxide Nutrition 0.000 claims description 56
- 235000008733 Citrus aurantifolia Nutrition 0.000 claims description 17
- 235000011941 Tilia x europaea Nutrition 0.000 claims description 17
- 239000004571 lime Substances 0.000 claims description 17
- 235000019738 Limestone Nutrition 0.000 claims description 16
- 239000006028 limestone Substances 0.000 claims description 16
- 238000007664 blowing Methods 0.000 claims description 8
- 238000005245 sintering Methods 0.000 claims description 5
- 238000011144 upstream manufacturing Methods 0.000 claims description 5
- 239000000567 combustion gas Substances 0.000 description 23
- 238000010304 firing Methods 0.000 description 21
- 238000002485 combustion reaction Methods 0.000 description 18
- 239000007789 gas Substances 0.000 description 11
- 239000000446 fuel Substances 0.000 description 8
- 239000000295 fuel oil Substances 0.000 description 8
- 238000001354 calcination Methods 0.000 description 7
- 238000001816 cooling Methods 0.000 description 6
- 238000005338 heat storage Methods 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- 239000000463 material Substances 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 238000002347 injection Methods 0.000 description 3
- 239000007924 injection Substances 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 239000012717 electrostatic precipitator Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000005979 thermal decomposition reaction Methods 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000003570 air Substances 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 235000010261 calcium sulphite Nutrition 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000006477 desulfuration reaction Methods 0.000 description 1
- 230000023556 desulfurization Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000004449 solid propellant Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Landscapes
- Vertical, Hearth, Or Arc Furnaces (AREA)
Description
[産業上の利用分野]
本発明は内熱式の竪型石灰焼成装置に係り、特
に硫黄分(以下S分という)の少ない生石灰の製
造を可能にした竪型石灰焼成装置に関する。
[従来の技術]
立設されたシヤフトの頂部に石灰石装入手段を
またシヤフトの底部に焼成物の排出機構を設け、
塊状石灰石をこのシヤフト内に導入してその焼成
を行う竪型石灰焼成装置が周知である。
この装置では、例えば特公昭51−21638号及び
特開昭58−26054号等に示される如く、シヤフト
が複数基並列に設けられ、これらが燃焼ガス及び
空気の通路である連結チヤンネルで接続され、交
互に燃焼と蓄熱との切替えが行われて焼成される
こともある。
このような竪型石灰焼成装置のシヤフト内で
は、石灰石(CaCO3)の熱分解により生石灰
(CaO)と炭酸ガス(CO2)とが生じる。一方、
重油等の燃料中に含まれる可燃性S分は600〜800
℃でSO2ガスとなり、燃焼ガスに混在する。
CaOは常温ではSO2を吸収しないが、300〜400
℃では吸収し、400℃以上では反応が速く、
CaSO3を生成する。更に400℃〜800℃になると、
CaSO3は部分的に分解してCaSとCaSO4となる。
即ち、下記の反応が行われる。
4CaSO3→3CaSO4+CaS
4CaO+4SO2→3CaSO4+CaS
なお、800℃以上ではCaCO3及びCaSは酸化さ
れてCaSO4となり、更に高温の1000℃以上では
CaOはSO2を吸収固定する能力が失う。
[発明が解決しようとする問題点]
而して、竪型石灰焼成装置においては、石灰石
の熱分解温度以上でかつなるべく低い温度で焼成
することにより、塊状生石灰の活性を高くすると
共に、熱原単位を下げるようにしており、従つ
て、焼成帯の一部(1200℃)をのぞいて大部分は
1000℃以下の温度になつている。そのため、従来
では、塊状生石灰に固定されるSO2が増大して製
品生石灰の品質が低下する恐れがありとりわけ燃
料のS分含有量が多い場合には、製品品質の低下
が生じ易かつた。
[問題点を解決するための手段]
上記問題点を解決するために、本発明者が鋭意
研究を重ねた結果、粒径の小さい生石灰ほど焼成
の過程で該生石灰粒子に固定されるS分が多くな
る傾向にあることが判明した。
本発明はこのような知見を基にして完成された
ものであり、焼成中の燃焼ガス中に微小生石灰を
含ませてS分を吸収(又は吸着)させ、塊状生石
灰に固定されるS分を大幅に低減するよう構成し
たものであつて、
上下方向に立設されたシヤフトを有し、該シヤ
フトにて塊状の石灰石の焼成を行う竪型石灰焼成
装置において、該シヤフト内に粉末生石灰を吹き
込む吹込手段と、吹き込まれた粉末生石灰が燃焼
ガスと接触し得る部位に設けた竪型石灰焼成装置
であつて、前記吹込手段は複数個設置されてお
り、そのうちの少なくとも1個は、シヤフトの焼
成帯または該焼成帯よりもガス流通上流側に設置
されていることを特徴とする竪型石灰焼成装置、
を要旨とするものである。
[作用]
吹込手段から粉末生石灰をシヤフト内に吹き込
むと、燃料の燃焼によつて発生するSO2は粉末生
石灰と反応して固定され、燃焼排ガス流と共に炉
外へ排出される。
而して、前述のように、粒度の小さい生石灰ほ
どSO2を吸収(又は吸着)し易いので、粉末生石
灰へのSO2の吸収(吸着)が塊状生石灰へのSO2
の吸収(吸着)に先行する。そのため、製品とな
る塊状生石灰に固定されるS分が大幅に減少され
る。特に、本発明にあつては、焼成帯及びそれよ
りもガス流通上流側の部位から粉末生石灰が吹き
込まれるので、燃焼ガス中のSO2は確実に粉末生
石灰に固定され、常時良好な品質の塊状生石灰を
焚き出すことが可能とされる。
[実施例]
以下、本発明の一実施例を図面を参照して説明
する。
第1図は2シヤフトタイプの竪型炉を示し、各
シヤフト1の頂部に石灰石装入手段2及び排ガス
出口3を設けている。このシヤフト1の上部に
は、重油等の液体燃料用主バーナ4を備えたバー
ナ室5付きのバーナアーチ6を内設している。ま
た、シヤフト1の下部には複数個の補助燃焼装置
7を設け、更に底部には、焼成物の排出機構とし
てテーブル型排出装置8を設けている。なお、各
シヤフト1は下部において互いに連結チヤネル9
で連通している。
而して、本実施例においては、バーナ室5内、
シヤフト上方の燃焼空気管10内及びシヤフト下
方の冷却空気管11に適宜個数の粉末生石灰吹込
み口12a,12b,12cをそれぞれ設けてい
る。そして、この吹込み口12a〜cから粉末生
石灰を分散供給するようにしている。これによ
り、燃焼ガス中のSO2を粉末生石灰に接触固定さ
せてCaSO4及びCaS等の形で炉外へ燃焼空気と共
に排出させる。なお排出された粉末はサイクロン
や電気集塵器(EP)などにより補集される。
なお、以下に本実施例装置における焼成作用を
説明する。
石灰石装入手段2のダンパ部により、一方のシ
ヤフト1aにその頂部から装入された塊状の石灰
石は、バーナアーチ6の両側を通つて降下する。
一方重油は主バーナ4において燃焼される。バー
ナ室5の容積が小さいので、重油の一部はガス化
して燃焼するが、大部分はガス化するに至らず、
塊状石灰石の表面を蔽つたままで予熱帯から焼
成帯を降下する過程でガス化し燃焼する。この
際の燃焼用空気はシヤフト頂部からシヤフト内に
圧入される。
重油の燃焼によつて生成した燃焼ガスは焼成帯
を下降し、次いで中央部の連結チヤネル9を経
て他方のシヤフト1bに入り上昇に転じ、そのシ
ヤフト1b内の被焼成物にその保有する顕熱を与
え、排ガスとしてシヤフト1b頂部より排出され
る。
次のサイクルにおいては、石灰石装入手段2に
よる塊状石灰石の供給方向が切り替わり、他方の
シヤフト1bにおいて焼成が行われ、一方のシヤ
フト1aにおいてはシヤフト1bから導入された
燃焼ガスにより熱量が蓄えられる。このように両
シヤフト1a,1b間において交互に燃焼と蓄熱
との切替えが行われ操業が継続する。
次にシヤフト1a,1b内における内空気、燃
焼ガス及び被焼成物の流れを詳述する。なお第1
図において、空気及び燃焼ガスの流れをそれぞれ
実線及び破線で示す。また、以下燃焼側のシヤフ
トを燃焼シヤフト、蓄熱側のシヤフトを蓄熱シヤ
フトと称することがある。
一方のシヤフト1aが燃焼シヤフトの場合には
図に示すように、そのシヤフト1aの底部から導
入された冷却空気L1は、下降してくる焼成物を
冷却しつつ上昇し、連結チヤネル9で燃焼ガスと
合流して蓄熱シヤフトである他方のシヤフト1b
に入る。この場合、シヤフト1aでは、燃焼用空
気は頂部から圧入されるので、燃焼ガスは円錐形
状に拡散し、一方蓄熱シヤフトであるシヤフト1
bでは燃焼ガスの拡散は、シヤフト1bの底部か
ら導入された冷却空気L2の上昇流と相俟つて、
連結チヤネル9側に偏倚する。即ち、シヤフト内
に装入された被焼成物の空隙率の分布について測
定すると、壁面部の空隙率はシヤフト内部の空隙
率より大きい。そのためシヤフト1bの底部から
導入された冷却空気L2は、シヤフト1bの壁面
部に沿つて上昇し易くなるが、内壁側(即ちシヤ
フト1aに近い側)では、燃焼シヤフト1aから
の燃焼ガス流がエアカーテンのように流れ込んで
いるので、主として、外壁側(即ちシヤフト1a
から遠い側)に沿つて上昇することになり、その
結果上述したように、シヤフト1b内の燃焼ガス
の拡散は連続チヤンネル9側に偏倚する。
このように、竪型石灰焼成装置のシヤフト内部
においては、燃焼ガスは必ずしも均一には流れ
ず、部分的に偏倚したりする。
而して、本実施例においてはシヤフトの各所か
ら粉末生石灰が吹き込まれ、シヤフト1a,1b
のいずれを燃焼シヤフトとした場合においても、
常に、焼成帯及びそれよりもガス流通上流側の部
位から粉末生石灰が吹き込まれる。従つて、燃焼
ガス中のSO2は確実に粉末生石灰に固定され、常
時良好な品質の塊状生石灰を焚き出すことが可能
とされる。
また、このように粉末生石灰をシヤフト1内の
各所で供給するようにすれば、燃焼ガスと粉末生
石灰との接触が均一に行われるようになることか
ら、過度の供給による粉末生石灰の無駄もなく、
SO2を効率良く固定することができる。
また、本実施例において、バーナ室5、冷却空
気管11及び燃焼空気管10に設けた粉末生石灰
の吹込み口12a〜12cは、円周状に配列され
た適数の開口部を有し粉末生石灰を供給するもの
である。特にバーナ室5内の吹込み口12aは耐
熱性の高い合金又はセラミツク製の筒体により成
り、機械力又は圧縮空気によつて粉末生石灰を可
能なかぎり広角度に分散供給し、それによつて、
該粉末生石灰をバーナアーチ6の両側を降下して
くる塊状石灰石間に均一、かつ、より深く進入さ
せるようにするものである。これにより、粉末生
石灰をより一層均一に燃焼ガスと接触させること
が可能となる。
なお、吹き込まれる粉末生石灰の粒度が大きく
なると塊状の石灰石又は生石灰の間を通過しにく
くなるので、平均粒径が100μm以下程度のもの
がよい。
また、粉末生石灰の使用量は、燃料中のS分1
重量部に対し1〜5重量部程度が好ましい。使用
量が1重量部以下では効果が少なく、また、5重
量部を超えるとコストが高くなると共に、吹き込
まれた粉末生石灰はシヤフト中心部に集まり、全
体的な脱硫効果の増大はそれ程期待できない。
上記実施例においては、重油を燃料とする焼成
装置についれ説明したが、本発明は微粉炭あるい
はCOMなどを燃料としても良く、コークス等の
固体燃料と粉末生灰石を混合して又は粉末生石灰
と交互にシヤフト内に装入する焼成方式をも採用
し得る。
また、上記実施例では、所謂M窯を図示した
が、本発明は二重傾斜窯、二重円筒立窯、B窯、
S窯、N窯、国井式石灰重油焼成窯或いはクロス
ビーム型石灰焼成窯などその他の種々のタイプの
焼成装置にも適用できる。
好適な実験例を下記に示す。
この実験例では、補助燃焼装置7を省略した2
シヤフト焼成装置を用いた。燃料中S分1重量部
に対して3重量部の粉末生石灰を0.4Kg/cm2の圧
縮空気によつて80m3/Hrの割合で、粉末生石灰
供給口から分散供給し、バーナから噴射された重
油と共に燃焼ガス中に投入した。
製品生石灰中のS分量比較のためのサンプルは
製品排出ベルト上で約20分毎に300g程度、1日
36回、自動サンプル採取した。
第1表にその分析結果を示す。
[Industrial Application Field] The present invention relates to an internal heating type vertical lime calcining apparatus, and more particularly to a vertical lime calcining apparatus that makes it possible to produce quicklime with a low sulfur content (hereinafter referred to as S content). [Prior art] A limestone charging means is provided at the top of an upright shaft, and a fired material discharge mechanism is provided at the bottom of the shaft.
BACKGROUND OF THE INVENTION Vertical lime calcining apparatuses are well known in which limestone blocks are introduced into the shaft and calcined therein. In this device, as shown in Japanese Patent Publication No. 51-21638 and Japanese Patent Application Laid-Open No. 58-26054, a plurality of shafts are provided in parallel, and these are connected by a connecting channel that is a passage for combustion gas and air. Firing may also be performed by alternately switching between combustion and heat storage. In the shaft of such a vertical lime calcining device, quicklime (CaO) and carbon dioxide gas (CO 2 ) are generated by thermal decomposition of limestone (CaCO 3 ). on the other hand,
The flammable S content contained in fuel such as heavy oil is 600 to 800.
It becomes SO 2 gas at ℃ and is mixed in combustion gas. CaO does not absorb SO 2 at room temperature, but at 300-400
It absorbs at temperatures above 400 degrees Celsius, and reacts quickly at temperatures above 400 degrees Celsius.
Generate CaSO3 . Furthermore, when the temperature increases from 400℃ to 800℃,
CaSO 3 partially decomposes into CaS and CaSO 4 . That is, the following reaction is performed. 4CaSO 3 →3CaSO 4 +CaS 4CaO+4SO 2 →3CaSO 4 +CaS At temperatures above 800°C, CaCO 3 and CaS are oxidized to CaSO 4 , and at even higher temperatures above 1000°C,
CaO loses its ability to absorb and fix SO 2 . [Problems to be Solved by the Invention] Therefore, in the vertical lime calcining device, by firing at a temperature higher than the thermal decomposition temperature of limestone and as low as possible, the activity of lump quicklime is increased and the heat source is Therefore, except for a part of the firing zone (1200℃), most of the temperature is
The temperature is below 1000℃. Therefore, in the past, there was a risk that the SO 2 fixed in the lump quicklime would increase and the quality of the product quicklime would deteriorate, and especially when the S content of the fuel was high, the product quality was likely to deteriorate. [Means for Solving the Problems] In order to solve the above problems, the present inventor conducted intensive research and found that the smaller the particle size of quicklime, the less S content is fixed in the quicklime particles during the firing process. It turns out that there is a tendency to increase. The present invention was completed based on such findings, and involves incorporating minute quicklime into the combustion gas during firing to absorb (or adsorb) the S content, thereby removing the S content fixed in the lump quicklime. In a vertical lime sintering device that is configured to significantly reduce the amount of limestone and has a vertically erected shaft and uses the shaft to sinter lump limestone, powdered quicklime is blown into the shaft. A vertical lime firing device is provided with a blowing means and a part where the blown lime powder can come into contact with the combustion gas, and a plurality of said blowing means are installed, and at least one of the blowing means is used for firing the shaft. The gist of the invention is a vertical lime calcining apparatus characterized in that it is installed upstream of a belt or a firing zone in a gas flow direction. [Operation] When powdered quicklime is blown into the shaft from the blowing means, SO 2 generated by combustion of the fuel reacts with the powdered quicklime, is fixed, and is discharged out of the furnace together with the combustion exhaust gas flow. As mentioned above, the smaller the particle size of quicklime, the easier it is to absorb (or adsorb) SO 2 .
It precedes the absorption (adsorption) of Therefore, the S content fixed in the lump quicklime that becomes the product is significantly reduced. In particular, in the present invention, since powdered quicklime is injected from the firing zone and a region upstream of the gas flow, SO 2 in the combustion gas is reliably fixed in the powdered quicklime, and the lumps of good quality are always maintained. It is said that it is possible to burn quicklime. [Example] Hereinafter, an example of the present invention will be described with reference to the drawings. FIG. 1 shows a two-shaft type vertical furnace, in which a limestone charging means 2 and an exhaust gas outlet 3 are provided at the top of each shaft 1. A burner arch 6 with a burner chamber 5 equipped with a main burner 4 for liquid fuel such as heavy oil is installed in the upper part of the shaft 1. Further, a plurality of auxiliary combustion devices 7 are provided at the bottom of the shaft 1, and a table-type discharge device 8 is further provided at the bottom as a discharge mechanism for the fired product. In addition, each shaft 1 has a connecting channel 9 connected to each other at the lower part.
It communicates with Therefore, in this embodiment, inside the burner chamber 5,
An appropriate number of powder quicklime injection ports 12a, 12b, and 12c are provided in the combustion air pipe 10 above the shaft and in the cooling air pipe 11 below the shaft, respectively. Powdered quicklime is distributed and supplied from the blowing ports 12a to 12c. As a result, SO 2 in the combustion gas is fixed in contact with the powdered quicklime, and is discharged out of the furnace together with the combustion air in the form of CaSO 4 and CaS. The discharged powder is collected using a cyclone, electrostatic precipitator (EP), etc. The firing action in the apparatus of this embodiment will be explained below. By the damper part of the limestone charging means 2, the limestone lumps charged into one shaft 1a from the top thereof descend through both sides of the burner arch 6.
On the other hand, heavy oil is burned in the main burner 4. Since the volume of the burner chamber 5 is small, some of the heavy oil is gasified and burned, but the majority is not gasified.
While covering the surface of the limestone blocks, it gasifies and burns as it descends from the preheating zone to the firing zone. At this time, the combustion air is forced into the shaft from the top of the shaft. The combustion gas generated by the combustion of heavy oil descends through the firing zone, then enters the other shaft 1b through the connecting channel 9 in the center and turns upward, transferring the sensible heat it possesses to the material to be fired in the shaft 1b. and is discharged from the top of the shaft 1b as exhaust gas. In the next cycle, the direction in which the limestone charging means 2 supplies the lump limestone is switched, firing is performed in the other shaft 1b, and heat is stored in the one shaft 1a by the combustion gas introduced from the shaft 1b. In this way, switching between combustion and heat storage is performed alternately between both shafts 1a and 1b, and operation continues. Next, the flow of internal air, combustion gas, and materials to be fired in the shafts 1a and 1b will be described in detail. Note that the first
In the figure, the flows of air and combustion gas are shown by solid lines and broken lines, respectively. Further, hereinafter, the shaft on the combustion side may be referred to as a combustion shaft, and the shaft on the heat storage side may be referred to as a heat storage shaft. If one of the shafts 1a is a combustion shaft, as shown in the figure, the cooling air L1 introduced from the bottom of the shaft 1a rises while cooling the descending baked product, and is combusted in the connecting channel 9. The other shaft 1b which merges with the gas and serves as a heat storage shaft
to go into. In this case, in the shaft 1a, the combustion air is forced in from the top, so the combustion gas is diffused in a conical shape, while the shaft 1a, which is a heat storage shaft,
In b, the diffusion of combustion gases, together with the upward flow of cooling air L2 introduced from the bottom of shaft 1b,
It is biased toward the connection channel 9 side. That is, when measuring the porosity distribution of the material to be fired charged into the shaft, the porosity of the wall surface portion is larger than the porosity of the inside of the shaft. Therefore, the cooling air L2 introduced from the bottom of the shaft 1b tends to rise along the wall surface of the shaft 1b, but on the inner wall side (i.e., the side closer to the shaft 1a), the combustion gas flow from the combustion shaft 1a is Since it flows in like an air curtain, it mainly flows into the outer wall side (i.e. the shaft 1a).
As a result, as mentioned above, the diffusion of the combustion gases in the shaft 1b is biased towards the continuous channel 9 side. As described above, the combustion gas does not necessarily flow uniformly inside the shaft of the vertical lime burning apparatus, but may be partially biased. In this embodiment, powdered quicklime is blown into the shafts 1a and 1b.
No matter which one is used as the combustion shaft,
Powdered quicklime is always injected from the firing zone and a region upstream of the firing zone in the gas flow direction. Therefore, SO 2 in the combustion gas is reliably fixed in the powdered quicklime, making it possible to always burn out lumpy quicklime of good quality. In addition, by supplying powdered quicklime at various locations within the shaft 1 in this way, the combustion gas and powdered quicklime will come into contact evenly, so there will be no waste of powdered quicklime due to excessive supply. ,
SO 2 can be fixed efficiently. In addition, in this embodiment, the injection ports 12a to 12c for powdered quicklime provided in the burner chamber 5, the cooling air pipe 11, and the combustion air pipe 10 have an appropriate number of openings arranged in a circumferential manner. It supplies quicklime. In particular, the inlet 12a in the burner chamber 5 is made of a cylinder made of a highly heat-resistant alloy or ceramic, and uses mechanical force or compressed air to disperse and supply powdered quicklime over as wide an angle as possible, thereby
This powder quicklime is made to penetrate more uniformly and more deeply between the lumpy limestone descending on both sides of the burner arch 6. This makes it possible to bring the powdered quicklime into contact with the combustion gas more uniformly. In addition, if the particle size of the powdered quicklime to be blown becomes large, it becomes difficult to pass between lumpy limestone or quicklime, so it is preferable that the average particle size is about 100 μm or less. In addition, the amount of powdered quicklime used is 1 S content in the fuel.
It is preferably about 1 to 5 parts by weight. If the amount used is less than 1 part by weight, the effect will be small, and if it exceeds 5 parts by weight, the cost will increase and the blown lime powder will collect in the center of the shaft, so that the overall desulfurization effect cannot be expected to increase much. In the above embodiments, a calcination device that uses heavy oil as fuel has been described, but the present invention may use pulverized coal or COM as fuel, or mix solid fuel such as coke with powdered quicksilver or powdered quicklime. It is also possible to adopt a firing method in which the materials are alternately charged into the shaft. In addition, in the above embodiment, a so-called M kiln is illustrated, but the present invention can be applied to a double inclined kiln, a double cylindrical vertical kiln, a B kiln,
It can also be applied to various other types of firing equipment such as S kiln, N kiln, Kunii type lime heavy oil kiln, or cross beam type lime kiln. A suitable experimental example is shown below. In this experimental example, the auxiliary combustion device 7 is omitted.
A shaft firing device was used. 3 parts by weight of powdered quicklime per 1 part by weight of S content in the fuel was dispersed and supplied from the powdered quicklime supply port at a rate of 80m 3 /Hr using 0.4Kg/cm 2 compressed air, and was injected from the burner. It was put into the combustion gas along with heavy oil. Samples for comparing the amount of S in product quicklime were collected on the product discharge belt at approximately 300g every 20 minutes for one day.
Automatic samples were taken 36 times. Table 1 shows the analysis results.
【表】
※ 製品生石灰粒径
第1表より、本発明によれば、製品生石灰中の
S分を30〜50%程度低減できることが明らかであ
る。
[効果]
以上詳述したように、本発明は、竪型石灰焼成
装置において、シヤフト内に粉末生石灰を吹き込
んで燃焼ガスと接触させ、燃焼ガス中のSO2を粉
末生石灰に固定されてシヤフト内から排出し得る
ようにしたので、シヤフトから取出される製品生
石灰に含まれるS分を減少させ、製品品質の向上
を図すことができる。特に、本発明では焼成帯及
びそれよりもガス流通上流側の部位から粉末生石
灰が吹き込まれる。従つて、燃焼ガス中のSO2は
確実に粉末生石灰に固定され、常時良好な品質の
塊状生石灰を焚き出すことが可能とされる。さら
に、粉末生石灰をシヤフト内に複数箇所で供給す
るようにしたので、燃焼ガスと粉末生石灰との接
触が均一に行われるようになることから、過度の
供給による粉末生石灰の無駄もなく、SO2を効率
良く固定することができる。また、既存の焼成装
置を簡便な工事で本発明構造に改良し得るので、
実用性にも優れる。[Table] * Product quicklime particle size From Table 1, it is clear that according to the present invention, the S content in product quicklime can be reduced by about 30 to 50%. [Effects] As detailed above, the present invention provides a vertical lime firing apparatus in which powdered quicklime is blown into the shaft and brought into contact with combustion gas, and SO 2 in the combustion gas is fixed in the powdered quicklime and released into the shaft. Since the product can be discharged from the shaft, the S content contained in the product quicklime taken out from the shaft can be reduced and the product quality can be improved. Particularly, in the present invention, powdered quicklime is blown from the firing zone and a region upstream of the gas flow. Therefore, SO 2 in the combustion gas is reliably fixed in the powdered quicklime, making it possible to always burn out lumpy quicklime of good quality. Furthermore, since powdered quicklime is supplied into the shaft at multiple locations, the combustion gas and powdered quicklime come into contact evenly, so there is no wastage of powdered quicklime due to excessive supply, and SO 2 can be fixed efficiently. Additionally, existing firing equipment can be improved to the structure of the present invention with simple construction.
It is also highly practical.
第1図は本発明の一実施例を示す縦断面図であ
る。
1(1a,1b)……シヤフト、2……石灰石
装入手段、3……排ガス出口、4……主バーナ、
5……バーナ室、6……バーナアーチ、7……補
助燃焼装置、8……排出装置、12a,12b,
12c……粉末生石灰の吹込み口。
FIG. 1 is a longitudinal sectional view showing one embodiment of the present invention. 1 (1a, 1b)...shaft, 2...limestone charging means, 3...exhaust gas outlet, 4...main burner,
5... Burner chamber, 6... Burner arch, 7... Auxiliary combustion device, 8... Discharge device, 12a, 12b,
12c...Injection port for powdered quicklime.
Claims (1)
ヤフトにて塊状の石灰石の焼成を行う堅型石灰焼
成装置において、該シヤフト内に粉末生石灰を吹
き込む吹込手段を、吹き込まれた粉末生石灰が燃
焼ガスと接触し得る部位に設けた堅型石灰焼成装
置であつて、前記吹込手段は複数個設置されてお
り、そのうちの少なくとも1個は、シヤフトの焼
成帯または該焼成帯よりもガス流通上流側に設置
されていることを特徴とする堅型石灰焼成装置。1. In a vertical lime burning device that has a vertically erected shaft and uses the shaft to burn lump limestone, a blowing means for blowing powdered quicklime into the shaft is used to cause the blown powdered quicklime to combust. A vertical lime sintering device installed in a part that can come into contact with gas, wherein a plurality of the blowing means are installed, and at least one of them is installed in a sintering zone of the shaft or on the upstream side of the gas flow from the sintering zone. A vertical lime sintering device characterized by being installed in.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP26591884A JPS61146741A (en) | 1984-12-17 | 1984-12-17 | Vertical lime burning device |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP26591884A JPS61146741A (en) | 1984-12-17 | 1984-12-17 | Vertical lime burning device |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61146741A JPS61146741A (en) | 1986-07-04 |
| JPH0353265B2 true JPH0353265B2 (en) | 1991-08-14 |
Family
ID=17423900
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP26591884A Granted JPS61146741A (en) | 1984-12-17 | 1984-12-17 | Vertical lime burning device |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS61146741A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2712461C1 (en) * | 2016-03-04 | 2020-01-29 | Маерц Офенбау Аг | Furnace, furnace operation method (embodiments) |
-
1984
- 1984-12-17 JP JP26591884A patent/JPS61146741A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2712461C1 (en) * | 2016-03-04 | 2020-01-29 | Маерц Офенбау Аг | Furnace, furnace operation method (embodiments) |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS61146741A (en) | 1986-07-04 |
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