JPS6248131B2 - - Google Patents
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- Publication number
- JPS6248131B2 JPS6248131B2 JP55021537A JP2153780A JPS6248131B2 JP S6248131 B2 JPS6248131 B2 JP S6248131B2 JP 55021537 A JP55021537 A JP 55021537A JP 2153780 A JP2153780 A JP 2153780A JP S6248131 B2 JPS6248131 B2 JP S6248131B2
- Authority
- JP
- Japan
- Prior art keywords
- gas
- exhaust gas
- water
- injected
- hcl
- 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
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- Chimneys And Flues (AREA)
- Treating Waste Gases (AREA)
Description
【発明の詳細な説明】
本発明は廃棄物焼却炉に関し、特に焼却により
発生する高温排ガスの冷却と、排ガス中の酸性ガ
スの低減を効率よく行なえる焼却炉に関するもの
である。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a waste incinerator, and particularly to an incinerator that can efficiently cool high-temperature exhaust gas generated by incineration and reduce acid gas in the exhaust gas.
各種廃棄物の焼却の際に、高温の排ガスが発生
するが、これはある程度、冷却してのち集塵等の
工程に移るが、排ガスの冷却方式としては水噴射
方式、ボイラ方式およびこれらの組合せがあり、
各焼却炉ごとに使い分けられている。 When incinerating various types of waste, high-temperature exhaust gas is generated, which is cooled to some extent before being transferred to processes such as dust collection. Methods for cooling the exhaust gas include water injection, boiler, and combinations of these. There is,
They are used differently for each incinerator.
一方、排ガス中には塩化水素ガス(HCl)およ
び/またはイオウ酸化物ガス(SOx)が含まれて
おり、大気汚染防止のためにこれら酸性ガスは低
減させたのち排ガスを大気に放出することができ
る。これら酸化性ガスの低減は高温ガスの冷却と
別個に独立して、次に示すような種々の方法で行
なわれているが、各々に記載したような欠点があ
る。 On the other hand, exhaust gas contains hydrogen chloride gas (HCl) and/or sulfur oxide gas (SO x ), and in order to prevent air pollution, these acidic gases must be reduced before exhaust gas is released into the atmosphere. Can be done. The reduction of these oxidizing gases has been carried out separately and independently from the cooling of the high-temperature gas by various methods as shown below, but each method has the drawbacks described below.
(1) 湿式アルカリ吸収法
HCl及びSOxの低減法としては有望なものが
開発されているが、湿式法であるため排液の処
理、および低温多湿であるため白煙発生等の技
術的問題が多く、しかも装置も大きく、建設
費、ランニングコストも高いという欠点があ
る。(1) Wet alkaline absorption method A promising method for reducing HCl and SO x has been developed, but because it is a wet method, there are technical problems such as processing of waste liquid and white smoke generation due to the low temperature and high humidity. There are many problems, and the equipment is also large, and the construction and running costs are high.
(2) 湿式蒸発塔方式燃焼排ガス等を反応蒸発塔も
しくは充填塔に導びき、水酸化カルシウム
〔Ca(OH)2〕のスラリを該塔内で蒸発させ、該
排ガスと接触混合させることによつて、HClお
よび/又はSOxを、それぞれ塩化カルシウム
(CaCl2)、硫酸カルシウム(CaSO4)にして除
去する方法であるが、該排ガス温度が200〜350
℃の場合には、スラリの蒸発によつてガス温度
が低下するため、前述の反応によつて生成する
CaCl2、CaSO4および未反応のCa(OH)2これ
以外のダスト等を補集するために設けた電気集
じん器の低温腐蝕を生ずる恐れがあると同時に
白煙発生等の問題がある。また装置が大きく建
設費が高いうえ、スラリのハンドリングが容易
でないという欠点がある。(2) Wet evaporation tower method Combustion exhaust gas, etc. is led to a reaction evaporation tower or a packed tower, and a slurry of calcium hydroxide [Ca(OH) 2 ] is evaporated in the tower and mixed in contact with the exhaust gas. This method removes HCl and/or SO x by converting them into calcium chloride (CaCl 2 ) and calcium sulfate (CaSO 4 ), respectively, but the exhaust gas temperature is between 200 and 350.
℃, the gas temperature decreases due to the evaporation of the slurry, so the gas produced by the above reaction
There is a risk of low-temperature corrosion of the electrostatic precipitator installed to collect dust such as CaCl 2 , CaSO 4 , and unreacted Ca(OH) 2 , and there are also problems such as generation of white smoke. Another disadvantage is that the equipment is large and construction costs are high, and the slurry is not easy to handle.
(3) 高温乾式低減法
燃焼過程にある750〜950℃の高温ガス中に該
ガスに含まれるHClおよび/又はSOxに対して
炭酸カルシウム(CaCO3)もしくはCa(OH)2
を粉体もしくはスラリ状で該ガスと接触させ
HCl及びSOxをそれぞれCaCl2、CaSO4に転化
し、電気集塵器等の煤塵捕集器で捕集し、
HCl、SOxを除去する方法であるが、該反応生
成物であるCaCl2は470〜500℃及び680〜740℃
で混入されている他の塩類(NaCl、Na2SO4)
と複合塩を作り、溶融する性質を有しており、
噴射点近傍及び後流の燃焼器壁や、燃焼装置に
空気予熱器等の熱交換器が付帯している場合に
は、熱交換器の管群に溶融付着し、それぞれク
リンカ生成、管群閉塞をきたし、プラント性能
に著しい悪影響をもたらすことになるので実用
的には種々問題がある。(3) High-temperature dry reduction method Calcium carbonate (CaCO 3 ) or Ca(OH) 2 is added to HCl and/or SO x contained in high-temperature gas of 750 to 950°C during the combustion process.
is brought into contact with the gas in powder or slurry form.
Convert HCl and SO x to CaCl 2 and CaSO 4 respectively, and collect them with a dust collector such as an electrostatic precipitator.
Although this is a method to remove HCl and SO
Other salts (NaCl, Na 2 SO 4 ) mixed in
It has the property of forming a complex salt and melting it.
If the combustion equipment is equipped with a heat exchanger such as an air preheater, it will melt and adhere to the combustor wall near the injection point and downstream, or to the tube group of the heat exchanger, producing clinker and clogging the tube group, respectively. This results in a significant adverse effect on plant performance, which poses various practical problems.
(4) 低温乾式低減法
HClおよび/又はSOxを含むガスに対して該
ガス温度が200〜450℃の領域に前記該酸性ガス
の量に対して1〜4当量のCa(OH)2の粉体を
該ガスと接触、混合させ、HCl及びSOxをそれ
ぞれCaCl2、CaSO4に転化し、煤塵捕集器で捕
集し、HCl、SOxを除去する方法であるが、こ
の方法では実プラントにおいて安定して得られ
る低減率としては50%程度である。(4) Low - temperature dry reduction method For gas containing HCl and/or SO This method involves contacting and mixing the powder with the gas, converting HCl and SO x into CaCl 2 and CaSO 4 respectively, and collecting them with a dust collector to remove HCl and SO x . The reduction rate that can be stably obtained in an actual plant is about 50%.
上に挙げた従来の酸性ガス低減法では燃焼完了
後の排ガスと薬品との接触混合が中心課題で、混
合性を増加させるために薬品の滞留時間を増加さ
せる方法や、あるいは排ガスの管路中に障害物を
置く方法などが考えられているが、大きな効果は
上げられなかつた。 In the conventional acid gas reduction methods mentioned above, the main issue is the contact mixing of the exhaust gas and chemicals after combustion is completed, and methods of increasing the residence time of the chemicals to improve miscibility, or methods of increasing the residence time of chemicals in the exhaust gas pipes are considered. Methods such as placing obstacles in the area have been considered, but no significant results have been achieved.
本発明者等は従来の酸性ガス低減法よりも更に
効果的かつ実用的なHCl、SOxの低減法、すなわ
ち、酸性ガスと薬品との混合率が高く、設備費、
ランニングコスト等が安価で、機器の操作性も容
易、しかも従来の低温乾式低減法より高い低減率
が得られる方法を開発すべく鋭意研究を行なつた
結果、排ガス冷却と酸性ガスの除去を同時に行う
本発明に到達したものである。 The present inventors have developed a method for reducing HCl and SO x that is more effective and practical than conventional acid gas reduction methods, that is, it requires a high mixing ratio of acid gas and chemicals, reduces equipment costs,
As a result of intensive research to develop a method that has low running costs, easy equipment operation, and a higher reduction rate than the conventional low-temperature dry reduction method, we succeeded in developing a method that simultaneously cools exhaust gas and removes acid gas. This is what the present invention has achieved.
すなわち本発明は、廃棄物焼却炉の燃焼室上部
(以下、炉上部)の高温ガス存在領域にアルカリ
土類金属化合物(酸化物、水酸化物、炭酸塩等)
粉末噴射装置を設け、該噴射装置の下流近傍に水
噴射装置を設けてなることを特徴とする排ガス冷
却と、アルカリ土類金属化合物粉末による酸性ガ
ス除去とを一体化して行うことのできる廃棄物焼
却炉に関する。本発明では炉上部の水噴射装置の
上流近傍の高温の排ガス中に上記アルカリ土類金
属化合物粉末を噴射すると、高温排ガス中に噴射
された水は蒸発と共に体積が増大し、この体積変
化によつて接触混合率が上昇し、更に従来、酸性
ガスとアルカリ土類金属化合物粉末との反応は固
気反応であつたものが、噴射された水により固液
反応となつて反応性が高くなるなど、水噴射冷却
とアルカリ土類金属化合物粉末噴射との一体化に
より、酸性ガスの低減率が上昇するものである。 That is, the present invention provides a method for injecting alkaline earth metal compounds (oxides, hydroxides, carbonates, etc.) into the high-temperature gas existing region in the upper part of the combustion chamber (hereinafter referred to as the upper part of the furnace) of a waste incinerator.
Waste that can be integrated with exhaust gas cooling and acid gas removal using alkaline earth metal compound powder, characterized in that a powder injection device is provided and a water injection device is provided near the downstream of the injection device. Regarding incinerators. In the present invention, when the alkaline earth metal compound powder is injected into the high-temperature exhaust gas near the upstream of the water injection device in the upper part of the furnace, the volume of the water injected into the high-temperature exhaust gas increases as it evaporates, and this volume change causes As a result, the contact mixing ratio increases, and the reaction between acidic gas and alkaline earth metal compound powder, which was previously a solid-gas reaction, becomes a solid-liquid reaction due to the injected water, increasing reactivity. By integrating water jet cooling and alkaline earth metal compound powder jetting, the reduction rate of acid gas is increased.
本発明において、従来、別々に行なわれてきた
排ガスの冷却と酸性ガスの低減を炉上部で一体化
することにより次のような効果が奏せられる。 In the present invention, the following effects can be achieved by integrating exhaust gas cooling and acid gas reduction, which have conventionally been performed separately, in the upper part of the furnace.
従来の低温乾式低減法に比べ高い低減率が得
られ、ランニングコストも安い。 A higher reduction rate can be obtained than the conventional low-temperature dry reduction method, and running costs are also lower.
炉上部に水噴射装置を有する既設炉にアルカ
リ薬品噴射装置を新設するだけでよいので設備
費が安価であり、従来の酸性ガス低減装置のよ
うにスペースをとることもない。 Since it is only necessary to newly install an alkali chemical injection device to an existing furnace that has a water injection device in the upper part of the furnace, the equipment cost is low and it does not take up space unlike conventional acid gas reduction devices.
反応生成物及び余剰薬品が落下した場合でも
炉内に落下するため保守管理が容易であり、機
器の操作も容易である。 Even if reaction products and surplus chemicals fall, they fall into the furnace, making maintenance management easy and the equipment easy to operate.
本発明は各種廃棄物焼却炉に適用できるが、炉
上部に水噴射排ガス冷却装置を有する都市ごみ焼
却炉、産業廃棄物焼却炉等に好適である。 Although the present invention can be applied to various waste incinerators, it is suitable for municipal waste incinerators, industrial waste incinerators, etc. that have a water injection exhaust gas cooling device in the upper part of the incinerator.
本発明を適用した具体例を第1図に示す。これ
は水噴射ガス冷式ごみ焼却炉に、Ca(OH)2の噴
射用のノズルを新設したものである。 A specific example to which the present invention is applied is shown in FIG. This is a water-injection gas-cooled waste incinerator with a new nozzle for injecting Ca(OH) 2 .
まずアルカリ土類金属化合物粉末(以下、薬
品)供給系について説明する。搬送用空気が、ブ
ロア1及びゲートバルブ2によりその量を調整
し、流量計3で流量を計測し管路4を経て、粉体
供給装置に送られる。粉体供給装置はホツパ部
5、及びエジエクタ部6より構成され、この装置
によりライン4からの搬送用空気とホツパ部5か
らの薬品とが混合される。混合された薬品は管路
7、バルブ8を経て、噴射ノズル15に至り、噴
射される。 First, the alkaline earth metal compound powder (hereinafter referred to as chemical) supply system will be explained. The amount of conveying air is adjusted by a blower 1 and a gate valve 2, the flow rate is measured by a flow meter 3, and the air is sent to a powder supply device through a pipe 4. The powder supply device is composed of a hopper section 5 and an ejector section 6, and the conveying air from the line 4 and the chemical from the hopper section 5 are mixed by this device. The mixed chemicals pass through the pipe 7 and the valve 8, reach the injection nozzle 15, and are injected.
一方、水噴射ガス冷却式ごみ焼却炉はホツパ1
0よりごみが炉内に供給され、ストーカ11の上
で燃焼する。燃焼を完了した排ガスは水噴射ノズ
ル12より噴射された水滴により冷却され、水滴
はガス冷却室13内部で完全蒸発される。その
後、燃焼空気予熱用熱交換器14を経て集じん器
に至る。 On the other hand, the water-injected gas-cooled waste incinerator is Hoppa 1.
Garbage is supplied into the furnace from 0 and burned on the stoker 11. The exhaust gas that has completed combustion is cooled by water droplets injected from the water injection nozzle 12, and the water droplets are completely evaporated inside the gas cooling chamber 13. Thereafter, the combustion air passes through a heat exchanger 14 for preheating and reaches a dust collector.
一方、薬品噴射用ノズル15は水噴射ノズル1
2の上流に設置した。この場合、薬品噴射ノズル
15より噴射された粉体はガス冷却室13に入つ
た瞬間、水が蒸発するゾーンに入り、そこで排ガ
スと接触混合を起し、排ガス中の酸性ガスと粉体
との固液反応により該酸性ガスは大巾に低減され
る。また一部の余剰Ca(OH)2及び反応生成物は
ストーカ11上に落下する。 On the other hand, the chemical injection nozzle 15 is the water injection nozzle 1.
It was installed upstream of 2. In this case, the moment the powder injected from the chemical injection nozzle 15 enters the gas cooling chamber 13, it enters the zone where water evaporates, where it comes into contact with the exhaust gas and mixes with the powder. The acidic gas is greatly reduced by the solid-liquid reaction. In addition, some of the excess Ca(OH) 2 and reaction products fall onto the stoker 11.
実施例
第1図に示した薬品供給装置の付設された水噴
射ガス冷却式ごみ焼却炉(150t/d)を利用して
実験を行なつた結果を第2図に示す。この時の実
験条件は以下の通りである。EXAMPLE FIG. 2 shows the results of an experiment conducted using a water-injected gas-cooled waste incinerator (150 t/d) equipped with the chemical supply device shown in FIG. 1. The experimental conditions at this time were as follows.
薬品噴射ノズル位置でのガス温度 約1000℃
薬品噴射ノズル位置でのガス流量
約34000Nm3/h
排ガス冷却室内径 2.7m
水噴射量 約10t/h
低減率(%)計算法
薬品噴射前HCl濃度−薬品噴射後HCl濃度/薬品噴射前HCl濃度×100
薬品噴射前HCl濃度
300〜450ppm(O2 12%換算)
本実施例では、以下の2ケ所からCa(OH)2粉
体を噴射して実験を行なつた。 Gas temperature at the chemical injection nozzle position Approximately 1000℃ Gas flow rate at the chemical injection nozzle position
Approx. 34000Nm 3 /h Exhaust gas cooling chamber diameter 2.7m Water injection amount Approx. 10t/h Reduction rate (%) calculation method HCl concentration before chemical injection - HCl concentration after chemical injection / HCl concentration before chemical injection x 100 HCl concentration before chemical injection
300 to 450 ppm (calculated as O 2 12%) In this example, an experiment was conducted by injecting Ca(OH) 2 powder from the following two locations.
a ガス冷却室13上部より噴射した場合(第
2図、)
b 薬品噴射ノズル15より噴射した場合(第2
図、)
第2図から明らかなように同じ当量比では薬品
噴射直後に水が噴射される場合が酸性ガス低減率
が最も高い。これはケースaの場合、水は全て水
蒸気で反応も固気反応が中心であり、噴射した水
による脱塩効果はみとめられないものと考えられ
る。ケースbでは薬品が噴射した水接触すること
により、反応が固液反応及び気液反応が主体とな
り反応効率を上昇させる為と考えられる。a When the gas is injected from the upper part of the gas cooling chamber 13 (Fig. 2) b When it is injected from the chemical injection nozzle 15 (the second
As is clear from FIG. 2, at the same equivalence ratio, the acidic gas reduction rate is highest when water is injected immediately after chemical injection. This is because in case a, the water is all water vapor and the reaction is mainly a solid-gas reaction, so it is considered that the desalination effect of the injected water is not observed. In case b, it is thought that this is because the reaction is mainly a solid-liquid reaction and a gas-liquid reaction when the chemical comes into contact with the injected water, increasing the reaction efficiency.
第1図は本発明焼却炉の一具体例であり、第2
図は本発明の薬品噴射位置と酸性ガス低減率との
関係を示すグラフである。
Figure 1 shows a specific example of the incinerator of the present invention, and the second
The figure is a graph showing the relationship between the chemical injection position and the acid gas reduction rate of the present invention.
Claims (1)
域にアルカリ土類金属化合物粉末噴射装置を設
け、該噴射装置の下流近傍に水噴射装置を設けて
なることを特徴とする廃棄物焼却炉。1. A waste incinerator, characterized in that an alkaline earth metal compound powder injection device is provided in a high-temperature gas presence region above a combustion chamber of the waste incinerator, and a water injection device is provided near the downstream of the injection device.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2153780A JPS56119415A (en) | 1980-02-25 | 1980-02-25 | Waste incinerating furnace |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2153780A JPS56119415A (en) | 1980-02-25 | 1980-02-25 | Waste incinerating furnace |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS56119415A JPS56119415A (en) | 1981-09-19 |
| JPS6248131B2 true JPS6248131B2 (en) | 1987-10-12 |
Family
ID=12057707
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2153780A Granted JPS56119415A (en) | 1980-02-25 | 1980-02-25 | Waste incinerating furnace |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS56119415A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2017537297A (en) * | 2014-12-10 | 2017-12-14 | エバック オサケ ユキチュア | Waste treatment equipment |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3808485A1 (en) * | 1987-05-22 | 1989-09-28 | Energie Versorgungssyst Evs | METHOD AND DEVICE FOR BINDING HALOGENS TO SOLIDS IN THE COMBUSTION OF FOSSIL FUELS OR WASTE |
| JPH05261244A (en) * | 1992-03-17 | 1993-10-12 | Denka Consult & Eng Co Ltd | Method for removing hydrogen chloride in combustion gas |
| JPH05272722A (en) * | 1992-03-27 | 1993-10-19 | Hitachi Zosen Corp | Garbage incinerator |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS54102285A (en) * | 1978-01-30 | 1979-08-11 | Hitachi Plant Eng & Constr Co Ltd | Purifying method for exhaust gas of municipal incinerator |
-
1980
- 1980-02-25 JP JP2153780A patent/JPS56119415A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2017537297A (en) * | 2014-12-10 | 2017-12-14 | エバック オサケ ユキチュア | Waste treatment equipment |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS56119415A (en) | 1981-09-19 |
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