JPS6135893B2 - - Google Patents
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- Publication number
- JPS6135893B2 JPS6135893B2 JP53138662A JP13866278A JPS6135893B2 JP S6135893 B2 JPS6135893 B2 JP S6135893B2 JP 53138662 A JP53138662 A JP 53138662A JP 13866278 A JP13866278 A JP 13866278A JP S6135893 B2 JPS6135893 B2 JP S6135893B2
- Authority
- JP
- Japan
- Prior art keywords
- ash
- exhaust gas
- denitrification
- boiler
- inlet
- 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
Landscapes
- Treating Waste Gases (AREA)
- Processing Of Solid Wastes (AREA)
Description
【発明の詳細な説明】
本発明はNH3と硫酸との化合物を含む灰、例え
ば石炭燃焼排ガス中の灰を集塵してえられるNH3
と硫酸との化合物(以下NH3の硫酸塩という)を
含む灰の処理に関するものである。[Detailed Description of the Invention] The present invention uses ash containing a compound of NH 3 and sulfuric acid, such as NH 3 obtained by collecting dust from ash in coal combustion exhaust gas.
This relates to the treatment of ash containing a compound of NH 3 and sulfuric acid (hereinafter referred to as NH 3 sulfate).
石炭燃焼排ガスには窒素酸化物、灰、硫黄酸化
物が含まれる。公害防止の観点から、脱硝、集
塵、脱硫の各装置が設置される。脱硝はNH3を還
元剤とする接触還元法が使用される。この場合脱
硝後の排ガス中にはNH35〜20ppm程度残存す
る。また排ガス中には無水硫酸10〜20ppm、灰
分数g/Nm3ないし10数g/Nm3が含まれる。 Coal combustion exhaust gas contains nitrogen oxides, ash, and sulfur oxides. To prevent pollution, denitrification, dust collection, and desulfurization equipment will be installed. For denitrification, a catalytic reduction method using NH 3 as a reducing agent is used. In this case, approximately 5 to 20 ppm of NH 3 remains in the exhaust gas after denitrification. Further, the exhaust gas contains 10 to 20 ppm of sulfuric anhydride and ash content of several g/Nm 3 to several tens of g/Nm 3 .
脱硝酸の排ガスはエアヒータで熱回収され、温
度が200℃程度以下となり、次に電気集塵機にて
集塵が行われる。 Heat is recovered from the exhaust gas from denitrification using an air heater to bring the temperature down to about 200°C or less, and then dust is collected using an electrostatic precipitator.
排ガス中のNH3と無水硫酸はこの温度以下では
凝縮し、NH3の硫酸塩(硫安、酸性硫安など)が
生成し、灰に付着し、電気集塵器で捕集される。 Below this temperature, NH 3 and sulfuric anhydride in the exhaust gas condense, producing sulfates of NH 3 (ammonium sulfate, acidic ammonium sulfate, etc.), which adhere to the ash and are collected by an electrostatic precipitator.
NH3の硫酸塩が付着した灰は従来の用途並びに
処分方法が適用できない大きな間題が発生する。 Ash with NH 3 sulfate adhering to it poses a major problem in which conventional usage and disposal methods cannot be applied.
上記灰をフライアツシユセメントの原料にする
ため、ポルトランドセメントと混合してフライア
ツシユセメントとした場合、これを使用する現場
において水と混練作業時にセメントの遊離石灰と
NH3の硫酸塩が反応して、石こうを生成すると共
に、NH3を遊離して、その作業環境にNH3による
悪臭公害を発生させる。 In order to use the above ash as a raw material for fly ash cement, if it is mixed with Portland cement to make fly ash cement, the free lime of the cement will be mixed with water and mixed at the site where it is used.
The sulfate of NH 3 reacts to form gypsum and liberate NH 3 , causing NH 3 odor pollution in the working environment.
一方投棄ないし埋立処分においても灰自身が含
むアルカリ分の溶出によつて同様の反応が起り、
公害問題を起す。 On the other hand, when dumping or landfilling, a similar reaction occurs due to the elution of alkaline content contained in the ash itself.
Causes pollution problems.
本発明は上記問題を解決するために、灰から
NH3を除く新規な方法及びその方法を実施する装
置を提案する。本発明はボイラのエコノマイザ入
口からの排ガスを分取して、その高温ガスでNH3
の硫酸塩を含む灰を加熱することを特徴とし、ボ
イラ出口と脱硝装置入口とを連通させ、前記脱硝
装置のボイラ排ガス流れ方向下流側に順にエアヒ
ータ、電気集塵器を配置し、同電気集塵器で集塵
された灰の排出口と灰処理反応器とを灰を導く管
路で連通させ、前記脱硝装置の上流側の高温のボ
イラ排ガスの1部を抽出して前記灰処理反応器に
導く管路を設け、前記灰処理反応器内で処理され
た処理排ガスを前記脱硝装置入口上流側に戻す管
路を設けたことを特徴とする。350〜450℃のボイ
ラ排ガスで灰を加熱することによりNH3の硫酸塩
は熱分解し、無水硫酸とNH3となる。無水硫酸は
灰中のアルカリ分例えばカルシウムと反応して石
こうとなり、灰中に固定される。NH3はガスとな
つて排ガスとに含まれ、灰からはNH3が除去され
る。NH3を含む排ガスは脱硝装置入口のボイラ排
ガスに戻される。 In order to solve the above problems, the present invention aims to
A new method for removing NH 3 and an apparatus for carrying out the method are proposed. The present invention separates the exhaust gas from the inlet of the economizer of the boiler and converts the high-temperature gas into NH3.
The boiler outlet and the denitrification device inlet are connected to each other, and an air heater and an electric precipitator are arranged in this order on the downstream side of the denitrification device in the flow direction of the boiler exhaust gas. The outlet for the ash collected by the dust collector is communicated with the ash treatment reactor through a pipe line for introducing ash, and a portion of the high temperature boiler exhaust gas on the upstream side of the denitrification device is extracted and transferred to the ash treatment reactor. The present invention is characterized in that a pipe line is provided that leads to the ash treatment reactor, and a pipe line that returns the treated exhaust gas treated in the ash treatment reactor to the upstream side of the denitrification device inlet. By heating the ash with boiler exhaust gas at 350-450°C, the sulfate of NH3 is thermally decomposed and becomes sulfuric anhydride and NH3 . Sulfuric anhydride reacts with alkaline components such as calcium in the ash to form gypsum, which is fixed in the ash. NH 3 becomes a gas and is included in the exhaust gas, and NH 3 is removed from the ash. The exhaust gas containing NH 3 is returned to the boiler exhaust gas at the inlet of the denitrification equipment.
本発明によれば処理灰中にNH3が含まれていな
いため先に述べた二次公害を起こさない。また本
発明における加熱はボイラ排ガスを使用するため
新たな燃料が不用である。さらに分離除去した
NH3ガスを脱硝用のアンモニア源として利用でき
ると共に、排ガスなどの後始末が不用である。 According to the present invention, since NH 3 is not contained in the treated ash, the above-mentioned secondary pollution does not occur. Furthermore, since boiler exhaust gas is used for heating in the present invention, no new fuel is required. further separated and removed
NH 3 gas can be used as an ammonia source for denitrification, and there is no need to clean up after exhaust gas.
脱硝装置はボイラ排ガス中の窒素酸化物を除去
するものであり、ボイラ排ガスにその中の窒素酸
化物に対する当量のNH3を添加して、窒素酸化物
とNH3の接触反応を行わせ、窒素酸化物を窒素と
水に変え、窒素酸化物を除く装置である。 Denitrification equipment removes nitrogen oxides from boiler exhaust gas. It adds NH 3 to the boiler exhaust gas in an amount equivalent to the nitrogen oxides in it, causes a catalytic reaction between nitrogen oxides and NH 3 , and removes nitrogen. This is a device that converts oxides into nitrogen and water and removes nitrogen oxides.
灰処理によつて生成するNH3は処理排ガスがメ
イン排ガスに戻されて脱硝用として利用される。 The NH 3 generated by ash treatment is returned to the main exhaust gas and used for denitrification.
さらに処理排ガスの持つている熱も処理排ガス
がメイン排ガスに戻されるため、最終的にエアヒ
ータで熱回収され、熱損失は少ない。 Furthermore, since the heat contained in the treated exhaust gas is returned to the main exhaust gas, the heat is ultimately recovered by the air heater, resulting in less heat loss.
次に本発明を第1図に示す実施態様例に基づい
て具体的に説明する。 Next, the present invention will be specifically explained based on an embodiment example shown in FIG.
本発明に係る石炭焚ボイラ排ガス処理システム
はボイラ1、脱硝装置2、エアヒータ3、電気集
塵器4、脱硝装置5から構成される。 The coal-fired boiler exhaust gas treatment system according to the present invention includes a boiler 1, a denitration device 2, an air heater 3, an electrostatic precipitator 4, and a denitration device 5.
NH3の硫酸塩付着灰は電気集塵器4で捕集され
灰処理反応器6に送られる。灰処理反応器6にボ
イラ排ガス8の1部がバイパスされて供給され
る。 The NH 3 sulfate-adhered ash is collected by an electrostatic precipitator 4 and sent to an ash treatment reactor 6. A portion of the boiler exhaust gas 8 is bypassed and supplied to the ash treatment reactor 6 .
灰処理反応器6はキルン式あるいは気流搬送式
の気固の反応器であり、熱と物質移動が行われ
る。ボイラ排ガスの温度は350〜450℃位である。
灰の温度は100℃程度である。灰処理装置におい
て灰はボイラ排ガスによつて加熱され灰は300℃
以上となる。同時にNH3の硫酸塩は熱分解され、
NH3は排ガスに放散され、無水硫酸は石こうとな
る。 The ash treatment reactor 6 is a kiln-type or pneumatic conveyance-type gas-solid reactor, and heat and mass transfer are performed therein. The temperature of boiler exhaust gas is about 350 to 450°C.
The temperature of the ash is about 100℃. In the ash processing equipment, the ash is heated to 300℃ by boiler exhaust gas.
That's all. At the same time, the sulfate of NH3 is thermally decomposed,
NH 3 is dissipated into the exhaust gas, and sulfuric anhydride becomes gypsum.
NH3を含む排ガス9に示す。処理排ガス9は
300℃となり、必要に応じてサイクロンなどで集
じんされ(図示なし)、脱硝装置の入口に戻され
る。NH3を含まない灰10は灰処理装置から排出
される。 Exhaust gas containing NH 3 is shown in Figure 9. The treated exhaust gas 9 is
The temperature reaches 300°C, and if necessary, dust is collected using a cyclone (not shown) and returned to the inlet of the denitrification equipment. The NH 3 -free ash 10 is discharged from the ash treatment device.
実験例
第1図に示す装置で石炭焚ボイラ排ガスからえ
られた灰の処理実験を行つた。Experimental Example An experiment was conducted using the apparatus shown in Figure 1 to treat ash obtained from coal-fired boiler exhaust gas.
110℃の灰にNH3が硫安として0.2wt%含まれて
いる。 Ash at 110℃ contains 0.2wt% of NH 3 as ammonium sulfate.
エアヒータ出口のNH310ppm、SO320ppmであ
つた。 NH 3 and SO 3 at the air heater outlet were 10 ppm and 20 ppm, respectively.
上記灰を50Kg/hrの割合で直径2m長さ6mのキ
ルンに供給し、450℃のボイラ排ガスを300Nm3/
hr供給した。キルン出口にサイクロンを取付け飛
散した灰を捕集した。捕集した灰中の硫安濃度を
分析した結果、硫安濃度は0.004〜0.006wt%であ
つた。NH3の残存率は2〜3%であつた。 The above ash was supplied to a kiln with a diameter of 2 m and a length of 6 m at a rate of 50 Kg/hr, and the boiler exhaust gas at 450°C was fed at a rate of 300 Nm 3 /hr.
hr supplied. A cyclone was installed at the kiln outlet to collect the scattered ash. As a result of analyzing the ammonium sulfate concentration in the collected ash, the ammonium sulfate concentration was 0.004 to 0.006 wt%. The residual rate of NH 3 was 2-3%.
本発明の効果
脱硝装置入口排ガスをバイパスしてNH3の硫酸
塩付着灰を処理できた。Effects of the present invention By bypassing the exhaust gas at the inlet of the denitrification equipment, NH 3 sulfate-adhered ash could be treated.
処理灰中にNH3の残存が少ないため後処理に問
題がない処理NH3を脱硝用に利用される、加熱源
に排ガスを使用するため、ユーテイリライの節
約、二次公害の発生がない。 Since there is little residual NH 3 in the treated ash, there is no problem with post-treatment. The treated NH 3 is used for denitrification. Because exhaust gas is used as the heating source, utility costs are saved and no secondary pollution occurs.
図は本発明の実施の態様例を示すブロツクダイ
ヤグラムである。
1……ボイラ、2……脱硝装置、3……エアー
ヒータ、4……電気集塵器、5……脱硫装置、6
……灰処理反応器、7……NH3の硫酸塩付着灰、
8……ボイラ排ガス、9……NH3含有処理排ガ
ス、10……アンモニアを含まない灰。
The figure is a block diagram showing an example of an embodiment of the present invention. 1...Boiler, 2...Denitration device, 3...Air heater, 4...Electrostatic precipitator, 5...Desulfurization device, 6
...Ash treatment reactor, 7... NH3 sulfate adhering ash,
8...Boiler exhaust gas, 9...Processed exhaust gas containing NH3 , 10...Ammonia-free ash.
Claims (1)
コノマイザ入口の高温ガスで加熱して、付着アン
モニウム塩を熱分解し、NH3を含むガスをえて、
該ガスを脱硝装置の入口に戻すことを特徴とする
NH3と硫酸との化合物を含む灰の処理方法。 2 ボイラ出口と脱硝装置入口とを連通させ、前
記脱硝装置のボイラ排ガス流れ方向下流側に順に
エアヒータ、電気集塵器を配置し、同電気集塵器
で集塵された灰の排出口と灰処理反応器とを灰を
導く管路で連通させ、前記脱硝装置の上流側の高
温のボイラ排ガスの1部を抽出して前記灰処理反
応器に導く管路を設け、前記灰処理反応器内で処
理された処理排ガスを前記脱硝装置入口上流側に
戻す管路を設けたことを特徴とする灰処理装置。[Claims] 1. Ash containing a compound of NH 3 and sulfuric acid is heated with high-temperature gas at the inlet of a boiler economizer to thermally decompose adhering ammonium salts and obtain a gas containing NH 3 .
The gas is returned to the inlet of the denitrification device.
Method for processing ash containing compounds of NH 3 and sulfuric acid. 2. The boiler outlet and the denitrification equipment inlet are communicated, and an air heater and an electrostatic precipitator are arranged in order on the downstream side of the boiler exhaust gas flow direction of the denitrification equipment, and the ash discharge port and the ash collected by the electrostatic precipitator are arranged in order. The processing reactor is connected to the ash processing reactor through a pipe line that leads ash, and a pipe line is provided to extract a part of the high temperature boiler exhaust gas upstream of the denitrification device and lead to the ash processing reactor, An ash processing device characterized in that a pipe line is provided for returning the treated exhaust gas to the upstream side of the denitrification device inlet.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13866278A JPS5564826A (en) | 1978-11-10 | 1978-11-10 | Treatment method for ash |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13866278A JPS5564826A (en) | 1978-11-10 | 1978-11-10 | Treatment method for ash |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5564826A JPS5564826A (en) | 1980-05-15 |
| JPS6135893B2 true JPS6135893B2 (en) | 1986-08-15 |
Family
ID=15227199
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP13866278A Granted JPS5564826A (en) | 1978-11-10 | 1978-11-10 | Treatment method for ash |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5564826A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10787564B2 (en) | 2018-01-11 | 2020-09-29 | Exxonmobil Chemical Patents Inc. | Polyethylene compositions and articles manufactured therefrom |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5632463U (en) * | 1979-08-20 | 1981-03-30 | ||
| JPS5637037A (en) * | 1979-09-03 | 1981-04-10 | Kawasaki Heavy Ind Ltd | Removing method of ammonium compound from coal ash |
| JPS56161822A (en) * | 1980-05-13 | 1981-12-12 | Kawasaki Heavy Ind Ltd | Removal of ammonium compound from coal ash |
-
1978
- 1978-11-10 JP JP13866278A patent/JPS5564826A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10787564B2 (en) | 2018-01-11 | 2020-09-29 | Exxonmobil Chemical Patents Inc. | Polyethylene compositions and articles manufactured therefrom |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5564826A (en) | 1980-05-15 |
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