JPH0677662B2 - Waste incinerator exhaust gas treatment method - Google Patents
Waste incinerator exhaust gas treatment methodInfo
- Publication number
- JPH0677662B2 JPH0677662B2 JP7093687A JP7093687A JPH0677662B2 JP H0677662 B2 JPH0677662 B2 JP H0677662B2 JP 7093687 A JP7093687 A JP 7093687A JP 7093687 A JP7093687 A JP 7093687A JP H0677662 B2 JPH0677662 B2 JP H0677662B2
- Authority
- JP
- Japan
- Prior art keywords
- exhaust gas
- incinerator
- ash
- chlorine compounds
- cooling
- 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 - Fee Related
Links
- 238000000034 method Methods 0.000 title claims description 9
- 239000002699 waste material Substances 0.000 title claims description 7
- 239000007789 gas Substances 0.000 claims description 31
- 238000001816 cooling Methods 0.000 claims description 25
- 239000000428 dust Substances 0.000 claims description 14
- 239000002912 waste gas Substances 0.000 claims description 2
- 150000001805 chlorine compounds Chemical class 0.000 description 13
- 239000012717 electrostatic precipitator Substances 0.000 description 12
- 150000004045 organic chlorine compounds Chemical class 0.000 description 11
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
- -1 aromatic chlorine compounds Chemical class 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000012716 precipitator Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000004056 waste incineration Methods 0.000 description 2
- OGBQILNBLMPPDP-UHFFFAOYSA-N 2,3,4,7,8-Pentachlorodibenzofuran Chemical compound O1C2=C(Cl)C(Cl)=C(Cl)C=C2C2=C1C=C(Cl)C(Cl)=C2 OGBQILNBLMPPDP-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 239000003905 agrochemical Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 101150085091 lat-2 gene Proteins 0.000 description 1
- NFBOHOGPQUYFRF-UHFFFAOYSA-N oxanthrene Chemical class C1=CC=C2OC3=CC=CC=C3OC2=C1 NFBOHOGPQUYFRF-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical class [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03C—MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03C3/00—Separating dispersed particles from gases or vapour, e.g. air, by electrostatic effect
- B03C3/01—Pretreatment of the gases prior to electrostatic precipitation
- B03C3/014—Addition of water; Heat exchange, e.g. by condensation
Landscapes
- Chimneys And Flues (AREA)
- Treating Waste Gases (AREA)
- Electrostatic Separation (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明はごみ焼却炉排ガスの処理法に関し、さらに詳し
くは有害な有機塩素化合物、特に芳香族系塩素化合物の
排出量を低減したごみ焼却炉排ガスの処理法に関するも
のである。TECHNICAL FIELD The present invention relates to a method for treating exhaust gas from a refuse incinerator, and more particularly to a refuse incinerator with reduced emission of harmful organic chlorine compounds, particularly aromatic chlorine compounds. The present invention relates to a method for treating exhaust gas.
人体にとって有害な有機塩素化合物、特に芳香族系塩素
化合物、例えばPCDD(ポリ塩素化ジベンゾダイオキシ
ン)、PCDF(ポリ塩素化ジベンゾフラン)等のような高
毒性の芳香族塩素系化合物は、農薬の副生物またはごみ
焼却の際の2次生成物質として生成され、環境を汚染す
ることが知られている(K.Olie et al, Chemosphere,
6, 455(1977)、およびT.Wakimoto et al, Environme
ntal Health Perspectives, 59, 159(1985))。この
うち、ごみ焼却の際に生成される有機塩素化合物を防止
する方法としては、従来、焼却炉の構造や焼却条件を検
討したり、スクラバー等の除去装置を付設することが行
なわれているが、それらの有害物質の発生原因について
は明らかではなく、有効な防止策を講じることはできな
かった。Organic chlorine compounds that are harmful to the human body, especially aromatic chlorine compounds, such as highly toxic aromatic chlorine compounds such as PCDD (polychlorinated dibenzodioxin) and PCDF (polychlorinated dibenzofuran), are by-products of agricultural chemicals. It is also known to be produced as a secondary product when incinerating waste and polluting the environment (K.Olie et al, Chemosphere,
6 , 455 (1977), and T. Wakimoto et al, Environme.
ntal Health Perspectives, 59 , 159 (1985)). Among them, as a method of preventing the organic chlorine compounds generated during refuse incineration, conventionally, the structure of the incinerator and the incineration conditions have been studied, and a scrubber removal device has been attached. However, the cause of these harmful substances was not clear, and effective preventive measures could not be taken.
本発明の目的は、ごみ焼却炉排ガス中に含まれる有機塩
素化合物、特に芳香族系有機塩素化合物の量を著しく低
減することができるごみ焼却炉排ガスの処理法を提供す
ることにある。It is an object of the present invention to provide a method for treating waste incinerator exhaust gas, which is capable of significantly reducing the amount of organic chlorine compounds, particularly aromatic organic chlorine compounds, contained in the waste incinerator exhaust gas.
本発明は、都市ごみ焼却炉排ガスを冷却後、集じん器で
除塵する都市ごみ焼却炉排ガスの処理方法において、焼
却炉出口から集じん器に到る間に排ガスを、少なくとも
300〜400℃の温度域の冷却速度が30〜100℃/secになる
ように250℃以下に急冷することを特徴とする。The present invention is a method for treating municipal waste incinerator exhaust gas in which dust is removed with a dust collector after cooling the municipal waste incinerator exhaust gas, and at least exhaust gas is discharged between the incinerator outlet and the dust collector.
It is characterized by rapid cooling to 250 ° C or less so that the cooling rate in the temperature range of 300 to 400 ° C is 30 to 100 ° C / sec.
次に本発明に到った経緯および実験結果について説明す
る。Next, the background of the present invention and the experimental results will be described.
第1図は、従来の典型的なごみ焼却処理施設のフローシ
ートである。ごみは焼却炉で約900℃で焼却処理され、
その排ガスはガス冷却塔で300℃に冷却された後、電気
集じん器に入り、ガスとEP灰とに分けられ、ガスは煙突
から系外に排出される。本発明者らは、このような焼却
処理施設の電気集じん器の前後から灰と排ガス試料を採
取し、その中に含有される有機塩素化合物の定量分析を
行なった。その結果を第1表に示す。また第1表の各有
機塩素化合物の濃度を示す値と排出量(平均値)の積か
ら該有機塩素化合物の発生量を求めた結果を第2表に示
す。第2表において、冷却塔灰、電気集じん器(EP)灰
およびEP出口ガスの値は、該ごみ焼却施設からのそれぞ
れ単位時間当たりの排出量(mg/H)に相当する。FIG. 1 is a flow sheet of a conventional typical waste incineration facility. Garbage is incinerated at about 900 ℃ in an incinerator,
The exhaust gas is cooled to 300 ℃ in the gas cooling tower, then enters the electrostatic precipitator, is separated into gas and EP ash, and the gas is discharged from the chimney to the outside of the system. The present inventors collected ash and exhaust gas samples from before and after the electrostatic precipitator of such an incineration facility, and quantitatively analyzed the organic chlorine compounds contained therein. The results are shown in Table 1. Further, Table 2 shows the results of obtaining the amount of the generated organic chlorine compound from the product of the value indicating the concentration of each organic chlorine compound in Table 1 and the emission amount (average value). In Table 2, the values of the cooling tower ash, the electrostatic precipitator (EP) ash, and the EP outlet gas correspond to the discharge amount (mg / H) per unit time from the waste incineration facility.
第1表の結果から、全般的にガス中の塩素化合物は電気
集じん器入口側より出口側が、また灰中の有機塩素化合
物は冷却塔灰より電気集じん器灰に多いことが認められ
た。From the results shown in Table 1, it was confirmed that chlorine compounds in the gas were generally present in the electric precipitator ash from the inlet side to the outlet side, and the organic chlorine compounds in the ash were higher in the electric precipitator ash than in the cooling tower ash. .
次に第2表の結果からは、電気集じん器からの灰と排ガ
ス中に含まれる塩素化合物の比率を比較すると、塩素数
の多い塩素化合物の方が、すなわち蒸気圧の低い方が灰
に吸着している比率が高くなる傾向が認められた。また
電気集じん器を通過するガス温度が低い場合、塩素化合
物は主に灰に、ガス温度が高い場合は塩素化合物は排ガ
ス中にその存在比が高くなることがわかった。Next, from the results in Table 2, comparing the ratio of the ash from the electrostatic precipitator and the chlorine compound contained in the exhaust gas, the chlorine compound with a higher chlorine number, that is, the one with a lower vapor pressure was converted to ash. It was recognized that the adsorbed ratio tended to increase. It was also found that when the temperature of the gas passing through the electrostatic precipitator is low, the chlorine compound becomes mainly ash, and when the gas temperature is high, the abundance ratio of the chlorine compound in the exhaust gas becomes high.
次に本発明者らは、冷却塔灰とEP灰について塩酸処理し
たものとしないもの合計4種類の試料についてそれぞれ
真空および酸素存在下において加熱温度および時間を変
化させて加熱試験を行なった。その結果を第3表に示
す。Next, the present inventors conducted a heating test on a total of four types of samples of the cooling tower ash and the EP ash that were treated with hydrochloric acid and not treated with hydrochloric acid in the presence of vacuum and oxygen while changing the heating temperature and time. The results are shown in Table 3.
第3表から明らかなように、冷却塔灰、EP灰ともに塩酸
処理した灰を酸素雰囲気下で300℃に加熱(実験No.17、
18、35および36参照)することによりきわめて多量の塩
素化合物が生成することがわかる。また塩酸処理した灰
ほど顕著ではないが、冷却塔灰、EP灰ともに加熱によっ
て塩素化合物が生成することがわかった。As is clear from Table 3, both the cooling tower ash and the EP ash treated with hydrochloric acid were heated to 300 ° C. in an oxygen atmosphere (Experiment No. 17,
18, 35 and 36), it is understood that an extremely large amount of chlorine compounds are produced. It was also found that chlorine compounds are produced by heating both the cooling tower ash and EP ash, although not as significantly as hydrochloric acid-treated ash.
以上のごみ焼却施設からの冷却塔灰および電気集塵灰の
実験結果から、従来焼却炉内で生成すると思われていた
有機塩素化合物、すなわちPCDD、PCDF、塩素化ベンゼ
ン、低級塩素化合物は大部分が300℃前後で電気集じん
器を通過する間に生成することが判明した。From the above experimental results of cooling tower ash and electric dust collection ash from the refuse incineration facility, most of the organic chlorine compounds that were thought to be generated in the incinerator, that is, PCDD, PCDF, chlorinated benzene, and lower chlorine compounds Was found to form during passing through an electrostatic precipitator at around 300 ° C.
以上の知見に基づき、本発明者らは、焼却炉を出た約75
0〜900℃の排ガスを、集じん器に入る前に冷却塔で250
℃以下、好ましくは199℃以下に急冷することにより、
排ガス中の有機塩素化合物を著しく低減できることを見
出し、本発明に到達した。Based on the above findings, the present inventors have found that about 75
Exhaust gas of 0 to 900 ℃ is cooled in the cooling tower before entering the dust collector.
By rapidly cooling to ℃ or less, preferably 199 ℃ or less,
They have found that the organic chlorine compounds in the exhaust gas can be significantly reduced, and have reached the present invention.
以下余白 本発明においては、焼却炉排ガスを、少なくとも300〜4
00℃の温度域の冷却速度が30〜100℃/secになるように2
50℃以下に急冷することにより、塩素化合物が発生し易
い温度域(300〜400℃)を速やかに通過するので、気相
中の塩素化合物の発生が抑制されるものと思われる。Margin below In the present invention, incinerator exhaust gas, at least 300 ~ 4
Set the cooling rate in the temperature range of 00 ℃ to 30-100 ℃ / sec. 2
By rapidly cooling to 50 ° C. or less, it rapidly passes through the temperature range (300 to 400 ° C.) where chlorine compounds are likely to be generated, so it is considered that the generation of chlorine compounds in the gas phase is suppressed.
本発明において、排ガスを急冷する場合の冷却速度は30
〜100℃/secが適当である。冷却速度が遅すぎると塩素
化合物の生成量が増加する300〜400℃の温度域を通過す
る時間が長くなり、排ガス中の塩素化合物の量が多くな
る。また250℃以下まで急冷しないと塩素化合物の発生
を充分に抑制することができない。In the present invention, the cooling rate when quenching the exhaust gas is 30
~ 100 ° C / sec is appropriate. If the cooling rate is too slow, the amount of chlorine compounds produced increases and the time for passing through the temperature range of 300 to 400 ° C. becomes long, and the amount of chlorine compounds in the exhaust gas increases. Moreover, unless it is rapidly cooled to 250 ° C. or less, generation of chlorine compounds cannot be sufficiently suppressed.
本発明において、高温の排ガスを急冷する装置としては
散水式の冷却塔、ボイラの熱交換器およびそれらの組合
せ等があげられる。冷却速度30〜100℃/secは、例えば
冷却水の量を調整することにより容易に得られる。また
冷却を行なう個所としては焼却炉と集じん器の間であれ
ばどこでもよいが、通常は焼却炉出口ガスの冷却部で行
なうのが望ましい。なお、集じん器は、乾式、半乾式、
湿式の電気集じん器の他、重力、遠心力、慣性力を利用
した集じん器、洗浄集じん器、濾過集じん器などのよう
な形式の集じん器でもよい。In the present invention, examples of a device for rapidly cooling high-temperature exhaust gas include a sprinkler type cooling tower, a boiler heat exchanger, and combinations thereof. The cooling rate of 30 to 100 ° C./sec can be easily obtained by adjusting the amount of cooling water, for example. Further, the place of cooling may be anywhere between the incinerator and the dust collector, but it is usually desirable to perform it in the cooling part of the incinerator outlet gas. The dust collector is a dry type, semi-dry type,
In addition to the wet type electric dust collector, dust collectors utilizing gravity, centrifugal force, inertial force, cleaning dust collector, filter dust collector and the like may be used.
本発明によれば、ごみ焼却炉排ガスを急冷することによ
り、有害な有機塩素化合物生成を効果的に抑制すること
ができる。According to the present invention, it is possible to effectively suppress the generation of harmful organic chlorine compounds by rapidly cooling the exhaust gas from the refuse incinerator.
第1図は、従来の都市ごみ焼却炉排ガスの処理方法の概
略フローを示す図である。FIG. 1 is a diagram showing a schematic flow of a conventional waste gas incinerator exhaust gas treatment method.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 高須賀 玄太郎 神奈川県横浜市西区浜松町4番19号 (56)参考文献 特開 昭49−27074(JP,A) 特開 昭60−84131(JP,A) ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Gentaro Takasuka 4-19 Hamamatsucho, Nishi-ku, Yokohama-shi, Kanagawa (56) References JP 49-27074 (JP, A) JP 60-84131 (JP, A)
Claims (1)
塵する都市ごみ焼却炉排ガスの処理方法において、焼却
炉出口から集じん器に到る間に排ガスを、少なくとも30
0〜400℃の温度域の冷却速度が30〜100℃/secになるよ
うに250℃以下に急冷することを特徴とするごみ焼却炉
排ガスの処理法。1. A method for treating municipal waste incinerator exhaust gas in which dust is removed by a dust collector after cooling the exhaust gas from the incinerator, and at least 30 exhaust gas is discharged from the outlet of the incinerator to the dust collector.
A method for treating waste gas from a refuse incinerator, which comprises rapidly cooling to 250 ° C or less so that the cooling rate in the temperature range of 0 to 400 ° C is 30 to 100 ° C / sec.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7093687A JPH0677662B2 (en) | 1987-03-25 | 1987-03-25 | Waste incinerator exhaust gas treatment method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7093687A JPH0677662B2 (en) | 1987-03-25 | 1987-03-25 | Waste incinerator exhaust gas treatment method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS63236513A JPS63236513A (en) | 1988-10-03 |
| JPH0677662B2 true JPH0677662B2 (en) | 1994-10-05 |
Family
ID=13445887
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP7093687A Expired - Fee Related JPH0677662B2 (en) | 1987-03-25 | 1987-03-25 | Waste incinerator exhaust gas treatment method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0677662B2 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02248368A (en) * | 1989-03-17 | 1990-10-04 | Toshiba Corp | Ceramics sintered body and production thereof |
| JPH0394813A (en) * | 1989-09-06 | 1991-04-19 | Japan Atom Energy Res Inst | Method for removing harmful gas in waste gas generated by incineration of refuse |
| JP2694631B2 (en) * | 1994-02-03 | 1997-12-24 | 株式会社タステム | High temperature exhaust gas forced rapid cooling device |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4927074A (en) * | 1972-07-08 | 1974-03-11 | ||
| JPS6084131A (en) * | 1983-10-17 | 1985-05-13 | Gadelius Kk | Waste gas treating method and apparatus thereof |
-
1987
- 1987-03-25 JP JP7093687A patent/JPH0677662B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPS63236513A (en) | 1988-10-03 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |