WO2020241379A1 - Incineration facility - Google Patents
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- WO2020241379A1 WO2020241379A1 PCT/JP2020/019781 JP2020019781W WO2020241379A1 WO 2020241379 A1 WO2020241379 A1 WO 2020241379A1 JP 2020019781 W JP2020019781 W JP 2020019781W WO 2020241379 A1 WO2020241379 A1 WO 2020241379A1
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23J—REMOVAL OR TREATMENT OF COMBUSTION PRODUCTS OR COMBUSTION RESIDUES; FLUES
- F23J15/00—Arrangements of devices for treating smoke or fumes
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- the present invention relates to an incineration facility that incinerates waste.
- Exhaust gas emitted from incineration facilities contains harmful substances such as nitrogen oxides, and it is necessary to remove harmful substances from the exhaust gas before it is released into the atmosphere in order to prevent air pollution.
- denitration of exhaust gas by reaction with a reducing agent is adopted.
- an incinerator that incinerates waste and an incinerator from this incinerator is equipped with a catalytic reaction tower that denitrates exhaust gas.
- the exhaust gas from the incinerator 1 is not denitrated as it is in the catalytic reaction tower 6, but is previously removed from the exhaust gas by the bag filter 3. Soot and dust are removed. Further, a filter cloth for filtering the soot and dust of the exhaust gas is installed in the bag filter 3, and since this filter cloth is damaged by the high temperature exhaust gas, the temperature reducing tower (EC) 2 is located on the upstream side of the bag filter 3. Be prepared.
- ammonia as a reducing agent.
- This method is also called an ammonia selective reduction method, and is a mainstream method for removing nitrogen oxides in exhaust gas.
- ammonia selective reduction method in an atmosphere in which the injected ammonia exists, it reacts with the sulfur oxide present in the exhaust gas to generate ammonium sulfate such as acidic ammonium sulfate. Therefore, the accumulation of ammonium sulfate on the catalyst in the catalytic reaction tower 6 lowers the catalytic activity. Further, the generated ammonium sulfate may cause the exhaust gas flow path to be blocked in the equipment downstream of the catalytic reaction tower 6.
- an object of the present invention is to provide an incineration facility capable of preventing a decrease in catalytic activity and blockage of an exhaust gas flow path with a simple configuration.
- the incinerator according to the first invention includes an incinerator that incinerates waste and an incinerator.
- a heating tower that cools the exhaust gas generated by incineration of the waste
- a bug filter that removes soot and dust from the cooled exhaust gas
- a reducing agent injection unit that injects a reducing agent for denitration into the exhaust gas from which soot and dust have been removed, It is provided with a catalytic reaction tower that promotes the reaction between the exhaust gas and the reducing agent by a catalyst.
- the reducing agent is alcohol or hydrocarbon
- the catalyst is a catalyst carrier containing MFI-type or FER-type zeolite on which at least one metal selected from the group consisting of Ag, Bi and Pb is supported.
- the alcohol as the reducing agent in the incineration facility according to the first invention is methanol or ethanol.
- the temperature of the exhaust gas is 130 ° C. to 200 ° C. in the catalytic reaction tower of the incineration facility according to the first or second invention.
- the incineration facility according to the fourth invention is the incineration facility according to the first or second invention without a reheating device for reheating the exhaust gas.
- the incineration facility it is not necessary to reheat the exhaust gas sent to the catalytic reaction tower, so that the configuration for reheating the exhaust gas required for the conventional incineration facility becomes unnecessary, and as a result, the configuration is simplified. Can be. Further, since the reducing agent of the incineration facility does not generate ammonium sulfate, it is possible to prevent a decrease in catalytic activity and blockage of the exhaust gas flow path due to the production of ammonium sulfate.
- the incineration facility 10 includes an incinerator 1 for incinerating waste, a temperature reducing tower 2 for reducing the temperature of exhaust gas generated by incineration of the waste, and soot dust from the reduced temperature exhaust gas. It is provided with a bug filter 3 for removing the above. Further, the incineration facility 10 includes a reducing agent injection unit 8 that injects a reducing agent for denitration into the exhaust gas from which soot and dust have been removed, and a catalytic reaction tower 6 that promotes the reaction between the exhaust gas and the reducing agent by a catalyst. To be equipped. Further, the incineration facility 10 may include a chimney 7 that discharges the denitrated exhaust gas into the atmosphere, if necessary.
- the reducing agent one that does not generate ammonium sulfate such as acidic ammonium sulfate, such as alcohol or hydrocarbon, is adopted. This is because ammonium sulfate may reduce the catalytic activity by accumulating on the catalyst and may cause the exhaust gas flow path to be blocked in the equipment downstream of the catalytic reaction tower 6.
- the catalyst one in which at least one metal selected from the group consisting of Ag, Bi and Pb is supported on a catalyst carrier containing MFI type or FER type zeolite is adopted.
- the exhaust gas into which the above-mentioned reducing agent (alcohol, hydrocarbon, etc.) that does not generate acidic ammonium sulfate is injected can be sufficiently denitrated even in a low temperature region of about 130 ° C. to 200 ° C. without reheating. .. Therefore, the incineration facility 10 does not need to have a reheater between the bag filter 3 and the catalytic reaction column 6.
- the alcohol as the reducing agent is not particularly limited as long as it has a reducing power at the temperature at the time of the reduction treatment of the combustion exhaust gas, but it is preferable to use methanol or ethanol which is an alcohol having a small number of carbon atoms.
- An inorganic acid salt for example, nitrate, chloride, etc.
- an organic acid salt for example, acetate, etc.
- zeolite zeolite
- examples thereof include an ion exchange method and an impregnation supporting method.
- zeolite is suspended in an aqueous solution containing a precursor compound of at least one metal selected from the group consisting of Ag, Bi, and Pb, and the zeolite to which the catalyst metal is bound by ion exchange is obtained. There is a method of taking it out of an aqueous solution, drying it, and then firing it.
- the shape of the catalyst can be arbitrarily selected depending on the reactor to be applied and the gas flow conditions, such as granular, pellet-shaped, honeycomb-shaped, and plate-shaped.
- the catalyst is preferably one in which zeolite is supported on a honeycomb structure made of an inorganic fiber sheet (including an inorganic fiber paper).
- the inorganic fiber sheet is preferably a glass fiber sheet or a ceramic fiber sheet.
- a honeycomb structure made of an inorganic fiber sheet as a base material
- a precursor compound of at least one metal selected from the group consisting of Ag, Bi, and Pb. Zeolite is suspended, and a base material of a honeycomb structure made of an inorganic fiber sheet is immersed in a catalyst component-containing slurry containing zeolite to which a catalyst metal is bonded by ion exchange, and after taking this out of the slurry, it is dried and 550. Bake below ° C.
- the honeycomb (honeycomb) structure refers to an integrated structure composed of a plurality of through holes (cells) partitioned by a partition and through which exhaust gas can flow, and the partition, and has a cross-sectional shape (of the cell) of the through holes.
- the cross-sectional shape is not particularly limited, and examples thereof include a circular shape, an arc shape, a square shape, a rectangular shape, and a hexagonal shape.
- a method (B) in which the glass fiber sheet, which is a material, is immersed in the sheet state is a method (A) of immersing the base material of the honeycomb structure in which an inorganic fiber sheet is previously assembled into a honeycomb (honeycomb) structure and a method (A) of immersing the base material of the honeycomb structure.
- zeolite was suspended in an aqueous solution containing a precursor compound of at least one metal selected from the group consisting of Ag, Bi, and Pb, and the catalyst metal was bonded by ion exchange.
- a honeycomb-shaped structure base material in which an inorganic fiber sheet is previously assembled into a honeycomb structure is immersed in a catalyst component-containing slurry containing zeolite, and after taking it out from the slurry, the conditions are 100 to 200 ° C. for 1 to 2 hours. After drying in, and further firing at 300 to 550 ° C. for 1 to 4 hours, the honeycomb structure substrate is provided with at least one catalytic metal selected from the group consisting of Ag, Bi, and Pb.
- a denitration catalyst is produced by binding the carried zeolite.
- the inorganic fiber sheet is preferably a glass fiber sheet or a ceramic fiber sheet.
- a honeycomb structure made of a glass fiber sheet is used as a base material, and a precursor compound of at least one metal selected from the group consisting of Ag, Bi, and Pb is contained.
- a catalyst component-containing slurry containing zeolite to which a catalyst metal is bound by ion exchange is prepared by suspending zeolite in an aqueous solution, and the catalyst component-containing slurry is applied to a glass fiber sheet to obtain a catalyst-containing slurry-coated glass fiber sheet.
- the catalyst-containing slurry-coated glass fiber sheet was shaped by a corrugated mold and a pressing jig, and the shaped corrugated plate-shaped catalyst-containing slurry-coated glass fiber sheet was placed at 100 to 200 ° C. for 1 to 2 hours. Dry under and peel from the mold, while flat plate-shaped, catalyst-containing slurry-coated fiberglass sheets that are not corrugated are dried at 100-200 ° C. for 1-2 hours and waved.
- a group consisting of Ag, Bi, and Pb obtained by firing a plate-shaped catalyst-containing slurry-coated glass fiber sheet and a flat plate-shaped catalyst-containing slurry-coated glass fiber sheet at 300 to 550 ° C. for 1 to 4 hours.
- a catalyst-supported flat glass fiber sheet and a catalyst-supported corrugated glass fiber sheet in which zeolite supporting at least one catalyst metal selected from the above are bonded are formed, and the catalyst-supported flat glass fiber sheet and the catalyst after firing are formed.
- a denitration catalyst is produced by laminating supported corrugated glass fiber sheets to form a catalyst-supported honeycomb structure.
- incinerator 1 when waste is incinerated, exhaust gas is generated by the incineration.
- This exhaust gas is sent to the temperature reducing tower 2, where the temperature is reduced to a temperature suitable for the bug filter 3 on the downstream side of the temperature decreasing tower 2.
- the bug filter 3 removes soot and dust from the exhaust gas from the temperature reducing tower 2.
- the exhaust gas from the bag filter 3 is injected with a reducing agent (alcohol, hydrocarbon, etc.) that does not generate acidic ammonium sulfate by the reducing agent injector 8 without being reheated.
- a reducing agent alcohol, hydrocarbon, etc.
- a catalyst metal (at least one metal selected from the group consisting of Ag, Bi and Pb) is supported on a catalyst carrier containing MFI-type or FER-type zeolite, and the exhaust gas is combined with the exhaust gas.
- the reaction with the reducing agent is promoted.
- nitrogen oxides are removed from the exhaust gas, that is, the exhaust gas is denitrated.
- the denitrated exhaust gas is released into the atmosphere from the chimney.
- the incineration facility 10 it is not necessary to reheat the exhaust gas sent to the catalytic reaction tower 6, so that the reheating device for reheating the exhaust gas required in the conventional incineration facility becomes unnecessary. As a result, the configuration can be simplified. Further, since the reducing agent of the incineration facility 10 does not generate ammonium sulfate (alcohol, hydrocarbon, etc.), it is possible to prevent a decrease in catalytic activity and blockage of the exhaust gas flow path due to the production of ammonium sulfate.
- ammonium sulfate alcohol, hydrocarbon, etc.
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Abstract
Description
本発明は、廃棄物の焼却を行う焼却施設に関するものである。 The present invention relates to an incineration facility that incinerates waste.
焼却施設から排出される排ガスには窒素酸化物などの有害物質が含まれており、大気汚染を防止するためにも、大気中に放出する前の排ガスから有害物質を除去する必要がある。排ガスから窒素酸化物を除去するには、排ガスを還元剤との反応により脱硝することが採用されている。具体的な焼却施設の構成としては、例えば、日本国特開2003-220317号公報(以下、特許文献1)に記載されているように、廃棄物を焼却する焼却炉と、この焼却炉からの排ガスを脱硝する触媒反応塔とを備える。 Exhaust gas emitted from incineration facilities contains harmful substances such as nitrogen oxides, and it is necessary to remove harmful substances from the exhaust gas before it is released into the atmosphere in order to prevent air pollution. In order to remove nitrogen oxides from exhaust gas, denitration of exhaust gas by reaction with a reducing agent is adopted. As a specific configuration of the incinerator, for example, as described in Japanese Patent Application Laid-Open No. 2003-220317 (hereinafter, Patent Document 1), an incinerator that incinerates waste and an incinerator from this incinerator. It is equipped with a catalytic reaction tower that denitrates exhaust gas.
前記特許文献1に記載の焼却施設では、当該特許文献1の図1に示すように、焼却炉1からの排ガスをそのまま触媒反応塔6で脱硝するのではなく、事前にバグフィルタ3で排ガスから煤塵が除去される。また、バグフィルタ3内には排ガスの煤塵を濾過するための濾布が設置されており、この濾布は高温の排ガスでは傷むので、バグフィルタ3の上流側に減温塔(EC)2が備えられる。
In the incineration facility described in Patent Document 1, as shown in FIG. 1 of Patent Document 1, the exhaust gas from the incinerator 1 is not denitrated as it is in the catalytic reaction tower 6, but is previously removed from the exhaust gas by the
ところで、前記特許文献1に記載の焼却施設では、減温塔(EC)2で減温された排ガスだと、触媒反応塔6では、低温のため触媒活性が低いので、それを補うための触媒量が必要になる。また、触媒反応塔6への排ガスの温度を上げるために、当該特許文献1の図1に示すように、触媒反応塔6の上流側に排ガスを加熱する蒸気式再加熱器5が備えられる。このように、前記焼却施設は、蒸気式再加熱器5を備えることにより、複雑な構成となってしまう。 By the way, in the incineration facility described in Patent Document 1, if the exhaust gas is cooled by the temperature reducing tower (EC) 2, the catalytic activity of the catalyst reaction tower 6 is low due to the low temperature, so a catalyst for supplementing the exhaust gas. Amount is needed. Further, in order to raise the temperature of the exhaust gas to the catalytic reaction tower 6, as shown in FIG. 1 of Patent Document 1, a steam type reheater 5 for heating the exhaust gas is provided on the upstream side of the catalytic reaction tower 6. As described above, the incineration facility has a complicated structure by providing the steam type reheater 5.
そして、アンモニアを還元剤として使用する方法もある。この方法は、アンモニア選択還元法とも言われ、排ガス中の窒素酸化物を除去する主流の方法である。しかしながら、これらの構成では、注入されたアンモニアが存在する雰囲気下において、排ガス中に存在する硫黄酸化物と反応して、酸性硫安などの硫安が生成されてしまう。このため、触媒反応塔6における触媒に硫安が堆積することで、触媒活性が低下する。さらには、生成した硫安によって、触媒反応塔6より下流の設備において排ガス流路の閉塞を招くおそれがある。 And there is also a method of using ammonia as a reducing agent. This method is also called an ammonia selective reduction method, and is a mainstream method for removing nitrogen oxides in exhaust gas. However, in these configurations, in an atmosphere in which the injected ammonia exists, it reacts with the sulfur oxide present in the exhaust gas to generate ammonium sulfate such as acidic ammonium sulfate. Therefore, the accumulation of ammonium sulfate on the catalyst in the catalytic reaction tower 6 lowers the catalytic activity. Further, the generated ammonium sulfate may cause the exhaust gas flow path to be blocked in the equipment downstream of the catalytic reaction tower 6.
そこで、本発明は、簡素な構成で、触媒活性の低下および排ガス流路の閉塞を防止し得る焼却施設を提供することを目的とする。 Therefore, an object of the present invention is to provide an incineration facility capable of preventing a decrease in catalytic activity and blockage of an exhaust gas flow path with a simple configuration.
前記課題を解決するため、第1の発明に係る焼却施設は、廃棄物を焼却する焼却炉と、
前記廃棄物の焼却により発生する排ガスを減温する減温塔と、
前記減温された排ガスから煤塵を除去するバグフィルタと、
前記煤塵が除去された排ガスに脱硝のための還元剤を注入する還元剤注入部と、
前記排ガスと還元剤との反応を触媒により促進させる触媒反応塔とを備え、
前記還元剤が、アルコールまたは炭化水素であり、
前記触媒が、MFI型またはFER型のゼオライトを含む触媒担体に、Ag、BiおよびPbよりなる群の中から選ばれた少なくとも1つの金属が担持されたものである。
In order to solve the above problems, the incinerator according to the first invention includes an incinerator that incinerates waste and an incinerator.
A heating tower that cools the exhaust gas generated by incineration of the waste,
A bug filter that removes soot and dust from the cooled exhaust gas,
A reducing agent injection unit that injects a reducing agent for denitration into the exhaust gas from which soot and dust have been removed,
It is provided with a catalytic reaction tower that promotes the reaction between the exhaust gas and the reducing agent by a catalyst.
The reducing agent is alcohol or hydrocarbon,
The catalyst is a catalyst carrier containing MFI-type or FER-type zeolite on which at least one metal selected from the group consisting of Ag, Bi and Pb is supported.
また、第2の発明に係る焼却施設は、第1の発明に係る焼却施設における前記還元剤としてのアルコールが、メタノールまたはエタノールである。 Further, in the incineration facility according to the second invention, the alcohol as the reducing agent in the incineration facility according to the first invention is methanol or ethanol.
さらに、第3の発明に係る焼却施設は、第1または第2の発明に係る焼却施設の前記触媒反応塔において、排ガスの温度が130℃~200℃である。 Further, in the incineration facility according to the third invention, the temperature of the exhaust gas is 130 ° C. to 200 ° C. in the catalytic reaction tower of the incineration facility according to the first or second invention.
加えて、第4の発明に係る焼却施設は、第1または第2の発明に係る焼却施設において、排ガスを再加熱する再加熱装置が無いものである。 In addition, the incineration facility according to the fourth invention is the incineration facility according to the first or second invention without a reheating device for reheating the exhaust gas.
前記焼却施設によると、触媒反応塔に送られる排ガスを再加熱する必要がないので、従来の焼却施設に必要であった排ガスを再加熱するための構成が不要になり、その結果、構成を簡素にすることができる。また、前記焼却施設の還元剤が硫安を生成させないものであるから、硫安の生成に由来する触媒活性の低下および排ガス流路の閉塞を防止することができる。 According to the incineration facility, it is not necessary to reheat the exhaust gas sent to the catalytic reaction tower, so that the configuration for reheating the exhaust gas required for the conventional incineration facility becomes unnecessary, and as a result, the configuration is simplified. Can be. Further, since the reducing agent of the incineration facility does not generate ammonium sulfate, it is possible to prevent a decrease in catalytic activity and blockage of the exhaust gas flow path due to the production of ammonium sulfate.
以下、本発明の実施の形態に係る焼却施設について、図面に基づき説明する。 Hereinafter, the incineration facility according to the embodiment of the present invention will be described with reference to the drawings.
図1に示すように、前記焼却施設10は、廃棄物を焼却する焼却炉1と、前記廃棄物の焼却により発生する排ガスを減温する減温塔2と、前記減温された排ガスから煤塵を除去するバグフィルタ3とを備える。また、前記焼却施設10は、前記煤塵が除去された排ガスに脱硝のための還元剤を注入する還元剤注入部8と、前記排ガスと還元剤との反応を触媒により促進させる触媒反応塔6とを備える。さらに、前記焼却施設10は、必要に応じて、脱硝された排ガスを大気中に放出する煙突7を備えてもよい。
As shown in FIG. 1, the
ここで、前記還元剤は、アルコールまたは炭化水素などの、酸性硫安などの硫安を発生させないものが採用される。なぜなら、硫安は、触媒に堆積することで触媒活性を低下させるとともに、触媒反応塔6より下流の設備において排ガス流路の閉塞を招くおそれがあるからである。前記触媒は、MFI型またはFER型のゼオライトを含む触媒担体に、Ag、BiおよびPbよりなる群の中から選ばれた少なくとも1つの金属が担持されたものが採用される。なぜなら、これにより、前述した酸性硫安を発生させない還元剤(アルコールまたは炭化水素など)が注入された排ガスを、再加熱しない130℃~200℃付近の低温領域でも、十分に脱硝し得るからである。従って、前記焼却施設10には、再加熱器をバグフィルタ3と触媒反応塔6との間に備える必要がない。
Here, as the reducing agent, one that does not generate ammonium sulfate such as acidic ammonium sulfate, such as alcohol or hydrocarbon, is adopted. This is because ammonium sulfate may reduce the catalytic activity by accumulating on the catalyst and may cause the exhaust gas flow path to be blocked in the equipment downstream of the catalytic reaction tower 6. As the catalyst, one in which at least one metal selected from the group consisting of Ag, Bi and Pb is supported on a catalyst carrier containing MFI type or FER type zeolite is adopted. This is because the exhaust gas into which the above-mentioned reducing agent (alcohol, hydrocarbon, etc.) that does not generate acidic ammonium sulfate is injected can be sufficiently denitrated even in a low temperature region of about 130 ° C. to 200 ° C. without reheating. .. Therefore, the
還元剤としてのアルコールは、燃焼排ガスの還元処理時の温度において還元力を有するものであれば、特に制限されるものではないが、炭素数の少ないアルコールであるメタノール、エタノールを用いることが好ましい。 The alcohol as the reducing agent is not particularly limited as long as it has a reducing power at the temperature at the time of the reduction treatment of the combustion exhaust gas, but it is preferable to use methanol or ethanol which is an alcohol having a small number of carbon atoms.
触媒としてゼオライトに担持する金属(以下、触媒金属)の前駆体化合物には、無機酸塩(例えば硝酸塩、塩化物など)や有機酸塩(例えば酢酸塩など)を用いることができる。触媒金属の担持方法は、脱硝性能が発揮できればよく、イオン交換法や含浸担持法などが挙げられる。例えばイオン交換法は、Ag、Bi、およびPbよりなる群の中から選ばれた少なくとも1つの金属の前駆体化合物を含む水溶液に、ゼオライトを懸濁させ、イオン交換により触媒金属が結合したゼオライトを水溶液から取り出して乾燥した後、焼成する方法がある。 An inorganic acid salt (for example, nitrate, chloride, etc.) or an organic acid salt (for example, acetate, etc.) can be used as a precursor compound of a metal supported on zeolite (hereinafter, catalyst metal) as a catalyst. As a method for supporting the catalyst metal, it is sufficient that the denitration performance can be exhibited, and examples thereof include an ion exchange method and an impregnation supporting method. For example, in the ion exchange method, zeolite is suspended in an aqueous solution containing a precursor compound of at least one metal selected from the group consisting of Ag, Bi, and Pb, and the zeolite to which the catalyst metal is bound by ion exchange is obtained. There is a method of taking it out of an aqueous solution, drying it, and then firing it.
前記触媒の形状は、粒状、ペレット状、ハニカム状、板状など、適用する反応器や、ガス流通条件により任意に選定することができる。前記触媒は、圧力損失の面から、無機繊維シート(無機繊維ペーパーを含む)で作られたハニカム構造体に、ゼオライトが担持されてなるものであることが好ましい。特に、無機繊維シートが、ガラス繊維シート、またはセラミック繊維シートであることが好ましい。 The shape of the catalyst can be arbitrarily selected depending on the reactor to be applied and the gas flow conditions, such as granular, pellet-shaped, honeycomb-shaped, and plate-shaped. From the viewpoint of pressure loss, the catalyst is preferably one in which zeolite is supported on a honeycomb structure made of an inorganic fiber sheet (including an inorganic fiber paper). In particular, the inorganic fiber sheet is preferably a glass fiber sheet or a ceramic fiber sheet.
前記触媒を、無機繊維シートよりなるハニカム構造体を基材として製造するには、例えば、Ag、Bi、およびPbよりなる群の中から選ばれた少なくとも1つの金属の前駆体化合物を含む水溶液に、ゼオライトを懸濁させ、イオン交換により触媒金属が結合したゼオライトを含む触媒成分含有スラリーに、無機繊維シートよりなるハニカム構造体の基材を浸漬し、これをスラリーから取り出した後、乾燥および550℃以下で焼成する。 To produce the catalyst using a honeycomb structure made of an inorganic fiber sheet as a base material, for example, in an aqueous solution containing a precursor compound of at least one metal selected from the group consisting of Ag, Bi, and Pb. , Zeolite is suspended, and a base material of a honeycomb structure made of an inorganic fiber sheet is immersed in a catalyst component-containing slurry containing zeolite to which a catalyst metal is bonded by ion exchange, and after taking this out of the slurry, it is dried and 550. Bake below ° C.
前記ハニカム(蜂の巣)構造体とは、隔壁により区画されかつ排ガスが流通可能な複数の貫通孔(セル)と当該隔壁とからなる一体形の構造体をいい、上記貫通孔の断面形状(セルの断面形状)は特に限定されず、例えば円形、円弧形、正方形、長方形、六角形が挙げられる。 The honeycomb (honeycomb) structure refers to an integrated structure composed of a plurality of through holes (cells) partitioned by a partition and through which exhaust gas can flow, and the partition, and has a cross-sectional shape (of the cell) of the through holes. The cross-sectional shape) is not particularly limited, and examples thereof include a circular shape, an arc shape, a square shape, a rectangular shape, and a hexagonal shape.
前記スラリーにハニカム構造体の基材を浸漬するには、予め無機繊維シートをハニカム(蜂の巣)構造に組み立てたハニカム構造体の基材を浸漬する方法(A)と、ハニカム構造体の基材の材料であるガラス繊維シートを、シート状態のまま浸漬する方法(B)とがある。 To immerse the base material of the honeycomb structure in the slurry, a method (A) of immersing the base material of the honeycomb structure in which an inorganic fiber sheet is previously assembled into a honeycomb (honeycomb) structure and a method (A) of immersing the base material of the honeycomb structure There is a method (B) in which the glass fiber sheet, which is a material, is immersed in the sheet state.
前記の方法(A)では、Ag、Bi、およびPbよりなる群の中から選ばれた少なくとも1つの金属の前駆体化合物を含む水溶液に、ゼオライトを懸濁させ、イオン交換により触媒金属が結合したゼオライトを含む触媒成分含有スラリーに、予め無機繊維シートをハニカム構造に組み立てたハニカム形状の構造体基材を浸漬し、これをスラリーから取り出した後、100~200℃で1~2時間の条件下で乾燥し、さらに300~550℃で1~4時間の条件下で焼成して、ハニカム構造体基材に、Ag、Bi、およびPbよりなる群の中から選ばれた少なくとも1つの触媒金属を担持したゼオライトを結合させることにより、脱硝触媒を製造するものである。前記の方法(A)の場合、無機繊維シートは、ガラス繊維シート、またはセラミック繊維シートであることが好ましい。 In the above method (A), zeolite was suspended in an aqueous solution containing a precursor compound of at least one metal selected from the group consisting of Ag, Bi, and Pb, and the catalyst metal was bonded by ion exchange. A honeycomb-shaped structure base material in which an inorganic fiber sheet is previously assembled into a honeycomb structure is immersed in a catalyst component-containing slurry containing zeolite, and after taking it out from the slurry, the conditions are 100 to 200 ° C. for 1 to 2 hours. After drying in, and further firing at 300 to 550 ° C. for 1 to 4 hours, the honeycomb structure substrate is provided with at least one catalytic metal selected from the group consisting of Ag, Bi, and Pb. A denitration catalyst is produced by binding the carried zeolite. In the case of the above method (A), the inorganic fiber sheet is preferably a glass fiber sheet or a ceramic fiber sheet.
これに対し、前記の方法(B)では、ガラス繊維シートよりなるハニカム構造体を基材とし、Ag、Bi、およびPbよりなる群の中から選ばれた少なくとも1つの金属の前駆体化合物を含む水溶液に、ゼオライトを懸濁させ、イオン交換により触媒金属が結合したゼオライトを含む触媒成分含有スラリーを調製して、ガラス繊維シートに触媒成分含有スラリーを塗布して触媒含有スラリー塗布ガラス繊維シートとし、ついで、触媒含有スラリー塗布ガラス繊維シートを波形付与金型と押さえ治具により形付けし、形付けされた波板状の触媒含有スラリー塗布ガラス繊維シートを100~200℃で1~2時間の条件下で乾燥し、金型から剥離し、一方、波板状に形付けしていない平板状の触媒含有スラリー塗布ガラス繊維シートを100~200℃で1~2時間の条件下で乾燥し、波板状の触媒含有スラリー塗布ガラス繊維シートと、平板状の触媒含有スラリー塗布ガラス繊維シートとを300~550℃で1~4時間の条件下で焼成して、Ag、Bi、およびPbよりなる群の中から選ばれた少なくとも1つの触媒金属を担持したゼオライトを結合した触媒担持平板状ガラス繊維シートおよび触媒担持波板状ガラス繊維シートを形成し、焼成後の触媒担持平板状ガラス繊維シートおよび触媒担持波板状ガラス繊維シートを積層して、触媒担持ハニカム構造体を形成することにより、脱硝触媒を製造するものである。 On the other hand, in the above method (B), a honeycomb structure made of a glass fiber sheet is used as a base material, and a precursor compound of at least one metal selected from the group consisting of Ag, Bi, and Pb is contained. A catalyst component-containing slurry containing zeolite to which a catalyst metal is bound by ion exchange is prepared by suspending zeolite in an aqueous solution, and the catalyst component-containing slurry is applied to a glass fiber sheet to obtain a catalyst-containing slurry-coated glass fiber sheet. Then, the catalyst-containing slurry-coated glass fiber sheet was shaped by a corrugated mold and a pressing jig, and the shaped corrugated plate-shaped catalyst-containing slurry-coated glass fiber sheet was placed at 100 to 200 ° C. for 1 to 2 hours. Dry under and peel from the mold, while flat plate-shaped, catalyst-containing slurry-coated fiberglass sheets that are not corrugated are dried at 100-200 ° C. for 1-2 hours and waved. A group consisting of Ag, Bi, and Pb obtained by firing a plate-shaped catalyst-containing slurry-coated glass fiber sheet and a flat plate-shaped catalyst-containing slurry-coated glass fiber sheet at 300 to 550 ° C. for 1 to 4 hours. A catalyst-supported flat glass fiber sheet and a catalyst-supported corrugated glass fiber sheet in which zeolite supporting at least one catalyst metal selected from the above are bonded are formed, and the catalyst-supported flat glass fiber sheet and the catalyst after firing are formed. A denitration catalyst is produced by laminating supported corrugated glass fiber sheets to form a catalyst-supported honeycomb structure.
以下、前記焼却施設10における排ガスの浄化方法について説明する。
Hereinafter, a method for purifying exhaust gas in the
図1に示すように、焼却炉1では、廃棄物が焼却されると、その焼却により排ガスが発生する。この排ガスは、減温塔2に送られ、そこで減温塔2の下流側にあるバグフィルタ3に適した温度まで減温される。バグフィルタ3では、減温塔2からの排ガスから煤塵が除去される。バグフィルタ3からの排ガスは、再加熱されることなく、還元剤注入器8により、酸性硫安を発生させない還元剤(アルコールまたは炭化水素など)が注入される。触媒反応塔6では、MFI型またはFER型のゼオライトを含む触媒担体に触媒金属(Ag、BiおよびPbよりなる群の中から選ばれた少なくとも1つの金属)が担持された触媒により、前記排ガスと還元剤との反応が促進される。この反応により、排ガスから窒素酸化物が除去され、つまり排ガスが脱硝される。脱硝された排ガスは、煙突から大気中に放出される。
As shown in FIG. 1, in incinerator 1, when waste is incinerated, exhaust gas is generated by the incineration. This exhaust gas is sent to the
このように、前記焼却施設10によると、触媒反応塔6に送られる排ガスを再加熱する必要がないので、従来の焼却施設に必要であった排ガスを再加熱する再加熱装置が不要になり、その結果、構成を簡素にすることができる。また、前記焼却施設10の還元剤が硫安を生成させないもの(アルコールまたは炭化水素など)であるから、硫安の生成に由来する触媒活性の低下および排ガス流路の閉塞を防止することができる。
As described above, according to the
Claims (4)
前記廃棄物の焼却により発生する排ガスを減温する減温塔と、
前記減温された排ガスから煤塵を除去するバグフィルタと、
前記煤塵が除去された排ガスに脱硝のための還元剤を注入する還元剤注入部と、
前記排ガスと還元剤との反応を触媒により促進させる触媒反応塔とを備え、
前記還元剤が、アルコールまたは炭化水素であり、
前記触媒が、MFI型またはFER型のゼオライトを含む触媒担体に、Ag、BiおよびPbよりなる群の中から選ばれた少なくとも1つの金属が担持されたものであること特徴とする焼却施設。 An incinerator that incinerates waste and
A heating tower that cools the exhaust gas generated by incineration of the waste,
A bug filter that removes soot and dust from the cooled exhaust gas,
A reducing agent injection unit that injects a reducing agent for denitration into the exhaust gas from which soot and dust have been removed,
It is provided with a catalytic reaction tower that promotes the reaction between the exhaust gas and the reducing agent by a catalyst.
The reducing agent is alcohol or hydrocarbon,
An incineration facility characterized in that the catalyst is a catalyst carrier containing MFI-type or FER-type zeolite on which at least one metal selected from the group consisting of Ag, Bi and Pb is supported.
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| JP2019-097231 | 2019-05-24 | ||
| JP2019097231A JP2020190396A (en) | 2019-05-24 | 2019-05-24 | Incineration facility |
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Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH1015355A (en) * | 1996-07-05 | 1998-01-20 | Kawasaki Heavy Ind Ltd | Denitration method and apparatus |
| JPH11165043A (en) * | 1997-12-04 | 1999-06-22 | Hitachi Zosen Corp | Exhaust gas treatment method for waste incinerator |
| JP2002301375A (en) * | 2001-01-31 | 2002-10-15 | Kubota Corp | Dioxin decomposition catalyst, decomposition treatment method and apparatus |
| WO2015119069A1 (en) * | 2014-02-07 | 2015-08-13 | 日立造船株式会社 | Catalyst and method for purifying combustion exhaust gas |
-
2019
- 2019-05-24 JP JP2019097231A patent/JP2020190396A/en active Pending
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2020
- 2020-05-19 WO PCT/JP2020/019781 patent/WO2020241379A1/en not_active Ceased
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH1015355A (en) * | 1996-07-05 | 1998-01-20 | Kawasaki Heavy Ind Ltd | Denitration method and apparatus |
| JPH11165043A (en) * | 1997-12-04 | 1999-06-22 | Hitachi Zosen Corp | Exhaust gas treatment method for waste incinerator |
| JP2002301375A (en) * | 2001-01-31 | 2002-10-15 | Kubota Corp | Dioxin decomposition catalyst, decomposition treatment method and apparatus |
| WO2015119069A1 (en) * | 2014-02-07 | 2015-08-13 | 日立造船株式会社 | Catalyst and method for purifying combustion exhaust gas |
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