JP2014001664A - Exhaust emission control device - Google Patents

Exhaust emission control device Download PDF

Info

Publication number
JP2014001664A
JP2014001664A JP2012136761A JP2012136761A JP2014001664A JP 2014001664 A JP2014001664 A JP 2014001664A JP 2012136761 A JP2012136761 A JP 2012136761A JP 2012136761 A JP2012136761 A JP 2012136761A JP 2014001664 A JP2014001664 A JP 2014001664A
Authority
JP
Japan
Prior art keywords
temperature
fuel
reformed gas
oxidation catalyst
exhaust
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.)
Granted
Application number
JP2012136761A
Other languages
Japanese (ja)
Other versions
JP6005413B2 (en
Inventor
Shinsuke Imai
伸介 今井
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hino Motors Ltd
Original Assignee
Hino Motors Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Hino Motors Ltd filed Critical Hino Motors Ltd
Priority to JP2012136761A priority Critical patent/JP6005413B2/en
Publication of JP2014001664A publication Critical patent/JP2014001664A/en
Application granted granted Critical
Publication of JP6005413B2 publication Critical patent/JP6005413B2/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02TCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
    • Y02T10/00Road transport of goods or passengers
    • Y02T10/10Internal combustion engine [ICE] based vehicles
    • Y02T10/12Improving ICE efficiencies

Landscapes

  • Exhaust Gas Treatment By Means Of Catalyst (AREA)
  • Exhaust Gas After Treatment (AREA)
  • Processes For Solid Components From Exhaust (AREA)

Abstract

PROBLEM TO BE SOLVED: To provide an exhaust emission control device capable of rising a temperature of an aftertreatment device of a selective reduction type catalyst and the like at an earlier stage than conventional.SOLUTION: An exhaust pipe 2 upstream of an oxidation catalyst 9 is provided with: a fuel addition device 10 (fuel addition means) for directly injecting fuel 8 in the exhaust pipe 2; and a modified gas addition device 12 (modified gas addition means) for dissolving the fuel 8 into modified gas 11 with high response and introducing it in the exhaust pipe 2. The modified gas 11 is introduced by the modified gas addition device 12 when a temperature of the oxidation catalyst 9 is not less than a first temperature that is an active lower limit temperature at which the modified gas 11 from the modified gas addition device 12 can be oxidized, and lower than a second temperature that is an active lower limit temperature at which the added fuel 8 from the fuel addition device 10 can be oxidized. The fuel 8 can be directly injected by the fuel addition device 10 when the temperature of the oxidation catalyst 9 is not less than the second temperature.

Description

本発明は、排気浄化装置に関するものである。   The present invention relates to an exhaust emission control device.

従来より、ディーゼルエンジンにおいては、排気ガスが流通する排気管の途中に、酸素共存下でも選択的にNOxを還元剤と反応させる性質を備えた選択還元型触媒を装備し、該選択還元型触媒の上流側に必要量の還元剤を添加して該還元剤を選択還元型触媒上で排気ガス中のNOx(窒素酸化物)と還元反応させ、これによりNOxの排出濃度を低減し得るようにしたものがある。   Conventionally, a diesel engine is equipped with a selective reduction catalyst having a property of selectively reacting NOx with a reducing agent even in the presence of oxygen in the middle of an exhaust pipe through which exhaust gas flows, and the selective reduction catalyst A required amount of a reducing agent is added to the upstream side of the catalyst so that the reducing agent undergoes a reduction reaction with NOx (nitrogen oxide) in the exhaust gas on the selective catalytic reduction catalyst, thereby reducing the NOx emission concentration. There is what I did.

他方、プラント等における工業的な排煙脱硝処理の分野では、還元剤にアンモニア(NH3)を用いてNOxを還元浄化する手法の有効性が既に広く知られているところであるが、自動車の場合には、アンモニアそのものを搭載して走行することに関し安全確保が困難であるため、近年においては、尿素水を還元剤として使用することが研究されている。 On the other hand, in the field of industrial flue gas denitration treatment in plants and the like, the effectiveness of a method for reducing and purifying NOx using ammonia (NH 3 ) as a reducing agent is already widely known. In recent years, it has been difficult to ensure the safety of traveling with ammonia itself, and in recent years, the use of urea water as a reducing agent has been studied.

即ち、尿素水を選択還元型触媒の上流側で排気ガス中に添加すれば、該排気ガスの熱によって尿素水が次式によりアンモニアと炭酸ガスに熱分解され、選択還元型触媒上で排気ガス中のNOxがアンモニアにより良好に還元浄化されることになる。
[化1]
(NH22CO+H2O→2NH3+CO2
That is, if urea water is added into the exhaust gas upstream of the selective catalytic reduction catalyst, the urea water is thermally decomposed into ammonia and carbon dioxide gas by the following equation by the heat of the exhaust gas, and the exhaust gas is exhausted on the selective catalytic reduction catalyst. The NOx contained therein is reduced and purified well by ammonia.
[Chemical 1]
(NH 2 ) 2 CO + H 2 O → 2NH 3 + CO 2

尚、この種の排気浄化装置に関連する先行技術文献情報としては下記の特許文献1等がある。   As prior art document information related to this type of exhaust purification device, there is the following Patent Document 1 and the like.

特開2002−161732号公報JP 2002-161732 A

しかしながら、このような排気浄化装置にあっては、選択還元型触媒の温度が約200℃程度まで上がらないと十分な触媒活性が得られないため、冷機始動時に選択還元型触媒の温度が約200℃程度に達するまで尿素水の添加を実施することができず、この間にNOxが浄化されないまま排出されてNOx低減率が大幅に低下してしまうという問題があった。   However, in such an exhaust purification device, sufficient catalytic activity cannot be obtained unless the temperature of the selective catalytic reduction catalyst reaches about 200 ° C. Therefore, the temperature of the selective catalytic reduction catalyst is about 200 at the time of cold start. The urea water cannot be added until the temperature reaches about 0 ° C., and during this time, NOx is discharged without being purified, and the NOx reduction rate is greatly reduced.

因みに、このような冷機始動時にあっては、エンジンの暖機が優先されて排気ガス再循環(EGR:Exhaust Gas Recirculation)も中止されるようになっているため、排気ガス再循環によりNOxを抑制することができないという事情もあった。   By the way, during such cold start, the engine warm-up is given priority and exhaust gas recirculation (EGR) is also stopped, so NOx is suppressed by exhaust gas recirculation. There was also a circumstance that it was not possible.

本発明は上述の実情に鑑みてなしたもので、選択還元型触媒等の後処理装置を従来より早期に昇温し得るようにした排気浄化装置を提供することを目的としている。   The present invention has been made in view of the above-described circumstances, and an object of the present invention is to provide an exhaust purification device that can raise the temperature of an aftertreatment device such as a selective catalytic reduction catalyst earlier than before.

本発明は、排気管途中の後処理装置より上流に酸化触媒を備え、該酸化触媒に対し燃料を添加して該燃料が前記酸化触媒上で酸化反応した時の反応熱により前記後処理装置の昇温を図り得るようにした排気浄化装置であって、前記酸化触媒より上流の排気管に、燃料を排気管内に直噴する燃料添加手段と、燃料を反応性の高い改質ガスに分解して排気管内に導入する改質ガス添加手段とを備え、前記酸化触媒の温度が前記改質ガス添加手段からの改質ガスを酸化処理可能な活性下限温度を成す第一温度以上で且つ前記燃料添加手段からの添加燃料を酸化処理可能な活性下限温度を成す第二温度を下まわっている時に前記改質ガス添加手段による改質ガスの導入を実施し、前記酸化触媒の温度が前記第二温度以上となっている時には燃料添加手段による燃料の直噴を実施し得るように構成したことを特徴とするものである。   The present invention includes an oxidation catalyst upstream of a post-treatment device in the middle of an exhaust pipe, and fuel is added to the oxidation catalyst, and the heat of the post-treatment device is generated by reaction heat when the fuel undergoes an oxidation reaction on the oxidation catalyst. An exhaust emission control device that can increase the temperature of the exhaust gas, the fuel adding means for directly injecting the fuel into the exhaust pipe upstream of the oxidation catalyst, and the fuel is decomposed into a highly reactive reformed gas. And a reformed gas adding means for introducing the fuel into the exhaust pipe, and the temperature of the oxidation catalyst is equal to or higher than a first temperature that forms a lower limit activation temperature at which the reformed gas from the reformed gas adding means can be oxidized, and the fuel The reformed gas is introduced by the reformed gas adding means when the added fuel from the adding means is lower than a second temperature that constitutes a minimum active temperature at which oxidation treatment is possible, and the temperature of the oxidation catalyst is set to the second temperature. When it is over temperature, add fuel It is characterized in that it has configured to be able to implement the direct injection of fuel by.

而して、このようにすれば、酸化触媒の温度が添加燃料を酸化処理可能な第二温度を下まわっていても、該第二温度より低い第一温度に達した段階で改質ガス添加手段による改質ガスの導入が実施され、その下流に配置されている酸化触媒にて反応性の高い改質ガスが酸化処理され、その反応熱により前記酸化触媒が急速に昇温して第二温度に達し、これにより改質ガス添加手段による改質ガスの導入から燃料添加手段による燃料の排気管内への直噴に切り替わり、活性の上がった酸化触媒にて添加燃料が直接的に酸化処理され、その反応熱で加熱された排気ガスが更に下流の後処理装置を通過することで該後処理装置が従来より早期に昇温されることになる。   Thus, in this way, even when the temperature of the oxidation catalyst is lower than the second temperature at which the added fuel can be oxidized, the reformed gas is added when the temperature reaches the first temperature lower than the second temperature. The reformed gas is introduced by the means, the highly reactive reformed gas is oxidized by the oxidation catalyst disposed downstream thereof, and the temperature of the oxidation catalyst is rapidly raised by the heat of reaction. As a result, the fuel is switched from the introduction of the reformed gas by the reformed gas adding means to the direct injection of the fuel into the exhaust pipe by the fuel adding means, and the added fuel is directly oxidized by the activated oxidation catalyst. The exhaust gas heated by the reaction heat further passes through the downstream aftertreatment device, so that the temperature of the aftertreatment device is raised earlier than before.

また、本発明においては、前記改質ガス添加手段が、燃料を反応性の高い改質ガスに分解する性質を備えた通気構造の改質触媒と、該改質触媒を収容して一端側を排気管内に開放したケーシングと、該ケーシングの他端側に接続されて改質ガスを一端側へ掃気するための搬送空気を導く搬送空気供給管と、前記ケーシングの他端側に接続されて燃料を前記改質触媒に供給する燃料供給管と、前記改質触媒を加熱する加熱手段とを備えていることが好ましい。   Also, in the present invention, the reformed gas adding means accommodates a reforming catalyst having a ventilation structure having the property of decomposing fuel into a reformed gas having high reactivity and one end side containing the reforming catalyst. A casing opened in the exhaust pipe, a carrier air supply pipe connected to the other end side of the casing to guide the carrier air for scavenging the reformed gas to one end side, and a fuel connected to the other end side of the casing It is preferable that a fuel supply pipe that supplies the reforming catalyst and a heating unit that heats the reforming catalyst are provided.

このように改質ガス添加手段を構成した場合、加熱手段により改質触媒を加熱して触媒活性を高めた上、該改質触媒に燃料供給管から燃料を供給し且つケーシングの他端側に搬送空気供給管から搬送空気を導くと、前記改質触媒にて燃料が反応性の高い改質ガスに分解されて搬送空気により排気管内に送り出されることになる。   When the reformed gas adding means is configured in this way, the reforming catalyst is heated by the heating means to increase the catalytic activity, and then the fuel is supplied to the reforming catalyst from the fuel supply pipe, and the other end of the casing is provided. When the carrier air is guided from the carrier air supply pipe, the fuel is decomposed into the reformed gas having high reactivity by the reforming catalyst and is sent out into the exhaust pipe by the carrier air.

また、本発明においては、前記改質ガス添加手段が、改質ガスに着火するための着火手段と、改質ガスの燃焼を助勢する燃焼空気を導く燃焼空気供給管とを備え、酸化触媒の温度が第一温度を下まわっている時に改質ガス添加手段により改質ガスを生成し且つ該改質ガスに着火してバーナ燃焼を実施し得るように構成されていることが好ましい。   In the present invention, the reformed gas adding means includes an ignition means for igniting the reformed gas, and a combustion air supply pipe for guiding combustion air for assisting the combustion of the reformed gas. It is preferable that when the temperature is lower than the first temperature, a reformed gas is generated by the reformed gas adding means, and the reformed gas is ignited to perform burner combustion.

このように改質ガス添加手段を構成した場合、酸化触媒の温度が第一温度を下まわっていても、改質ガス添加手段により生成された改質ガスが着火手段により着火され且つ燃焼空気供給管により燃焼空気が供給されることでバーナ燃焼が実施されるので、該バーナ燃焼により酸化触媒が速やかに昇温されて第一温度に達することになる。   When the reformed gas addition means is configured in this way, even if the temperature of the oxidation catalyst is lower than the first temperature, the reformed gas generated by the reformed gas addition means is ignited by the ignition means and the combustion air is supplied. Burner combustion is performed by supplying combustion air through the pipe, so that the oxidation catalyst is quickly heated by the burner combustion and reaches the first temperature.

上記した本発明の排気浄化装置によれば、下記の如き種々の優れた効果を奏し得る。   According to the exhaust emission control device of the present invention described above, various excellent effects as described below can be obtained.

(I)本発明の請求項1、2に記載の発明によれば、酸化触媒の温度が添加燃料を酸化処理可能な第二温度を下まわっている時に、該第二温度より低い第一温度に達した段階から改質ガス添加手段による改質ガスの導入を実施し、該改質ガスを下流の酸化触媒で酸化処理させることにより該酸化触媒を反応熱で急速に昇温して第二温度まで到達させることができ、これ以降は、改質ガス添加手段による改質ガスの導入から燃料添加手段による燃料の排気管内への直噴に切り替えることによって、活性の上がった酸化触媒にて添加燃料を直接的に酸化処理することで燃料の発熱量を最大限に利用して排気ガスを加熱し、該排気ガスを更に下流の後処理装置を通過させることで該後処理装置を従来より早期に昇温させることができ、例えば、後処理装置が尿素水を還元剤とする選択還元型触媒である場合には、該選択還元型触媒を冷機始動時でも早期に活性化させて尿素水の添加を従来より早い段階から開始することができ、冷機始動時におけるNOx低減率の大幅な向上を図ることができ、また、後処理装置がパティキュレートフィルタである場合には、該パティキュレートフィルタを排気温度の低い運転条件下でも早期にパティキュレート(煤分)を燃焼除去し得る再生温度まで到達させることができ、パティキュレートフィルタの再生時間の大幅な短縮を図ることができる。   (I) According to the first and second aspects of the present invention, when the temperature of the oxidation catalyst is lower than the second temperature at which the added fuel can be oxidized, the first temperature lower than the second temperature. The reformed gas is introduced by the reformed gas adding means from the stage of reaching the temperature, and the reformed gas is oxidized with the downstream oxidation catalyst to rapidly raise the temperature of the oxidation catalyst with the reaction heat. The temperature can be reached, and after that, by adding the reformed gas by the reformed gas adding means to the direct injection into the exhaust pipe of the fuel by the fuel adding means, it is added by the oxidation catalyst having increased activity. By directly oxidizing the fuel, the exhaust gas is heated using the maximum amount of heat generated by the fuel, and the exhaust gas is further passed through the downstream post-treatment device, thereby making the post-treatment device earlier than before. For example, after treatment When the apparatus is a selective reduction catalyst using urea water as a reducing agent, the selective reduction catalyst can be activated at an early stage even at the time of cold start so that the addition of urea water can be started at an earlier stage than before. The NOx reduction rate at the time of cold start can be greatly improved, and when the aftertreatment device is a particulate filter, the particulate filter can be particulated at an early stage even under operating conditions where the exhaust temperature is low. It is possible to reach a regeneration temperature at which (apportioned) can be removed by combustion, and the regeneration time of the particulate filter can be greatly shortened.

(II)本発明の請求項3に記載の発明によれば、酸化触媒の温度が第一温度を下まわっている時に、改質ガス添加手段により生成された改質ガスに着火手段で着火することによりバーナ燃焼を実施することができ、該バーナ燃焼により酸化触媒を速やかに昇温して第一温度まで上げることができるので、改質ガス添加手段による改質ガスの導入の開始時期を早め、延いては燃料添加手段による燃料の排気管内への直噴への切り替え時期を早めることができるので、後処理装置をより一層速やかに昇温することができる。   (II) According to the invention described in claim 3 of the present invention, when the temperature of the oxidation catalyst is lower than the first temperature, the reformed gas generated by the reformed gas addition means is ignited by the ignition means. As a result, burner combustion can be performed, and the oxidation catalyst can be quickly heated to the first temperature by the burner combustion, so that the start timing of introduction of the reformed gas by the reformed gas adding means can be advanced. As a result, the timing for switching to direct injection of fuel into the exhaust pipe by the fuel addition means can be advanced, so that the temperature of the post-treatment device can be raised even more quickly.

本発明を実施する形態の一例を示す概略図である。It is the schematic which shows an example of the form which implements this invention. 図1の改質ガス添加装置の詳細を示す断面図である。It is sectional drawing which shows the detail of the reformed gas addition apparatus of FIG. 図1の例における酸化触媒の出口温度の時間的な推移を示すグラフである。It is a graph which shows the time transition of the exit temperature of the oxidation catalyst in the example of FIG. 本発明の別の形態例を示す概略図である。It is the schematic which shows another form example of this invention. 図4の例における酸化触媒の出口温度の時間的な推移を示すグラフである。It is a graph which shows temporal transition of the exit temperature of the oxidation catalyst in the example of FIG.

以下本発明の実施の形態を図面を参照しつつ説明する。   Embodiments of the present invention will be described below with reference to the drawings.

図1は本発明を実施する形態の一例を示すもので、排気ガス1が流通する排気管2の途中に、酸素共存下でも選択的にNOxをアンモニアと反応させ得る性質を備えた選択還元型触媒3(後処理装置)が装備されており、該選択還元型触媒3の入側に、尿素水4を還元剤として添加する尿素水添加装置5が配置され、前記選択還元型触媒3の出側には、前記尿素水4から生成されて前記選択還元型触媒3で反応しないまま通過した余剰のアンモニアを酸化処理するアンモニア低減触媒6が装備されている。   FIG. 1 shows an example of an embodiment of the present invention. A selective reduction type having the property of selectively reacting NOx with ammonia even in the presence of oxygen in the middle of an exhaust pipe 2 through which exhaust gas 1 flows. A catalyst 3 (post-treatment device) is provided, and a urea water addition device 5 for adding urea water 4 as a reducing agent is disposed on the inlet side of the selective reduction catalyst 3. On the side, an ammonia reduction catalyst 6 that oxidizes excess ammonia that is generated from the urea water 4 and passes through the selective reduction catalyst 3 without reacting is provided.

また、前記尿素水添加装置5より上流側の排気管2には、排気ガス1中のパティキュレートを捕集するパティキュレートフィルタ7(後処理装置)が装備されており、該パティキュレートフィルタ7の入側には、排気ガス1に添加された燃料8を酸化処理し得る酸化触媒9が装備されている。   Further, the exhaust pipe 2 upstream of the urea water addition device 5 is equipped with a particulate filter 7 (post-treatment device) that collects particulates in the exhaust gas 1. On the inlet side, an oxidation catalyst 9 capable of oxidizing the fuel 8 added to the exhaust gas 1 is equipped.

そして、前記酸化触媒9より上流の排気管2に、燃料8を排気管2内に直噴する燃料添加装置10と、燃料8を反応性の高い改質ガス11に分解して排気管2内に導入する改質ガス添加装置12とが備えられており、これら燃料添加装置10と改質ガス添加装置12及び前記尿素水添加装置5の作動は制御装置13により制御信号13aを介して制御されるようになっている。   Then, a fuel addition device 10 for directly injecting fuel 8 into the exhaust pipe 2 to the exhaust pipe 2 upstream from the oxidation catalyst 9 and a reformed gas 11 having high reactivity are decomposed into the exhaust pipe 2. A reformed gas addition device 12 to be introduced into the fuel is provided, and the operations of the fuel addition device 10, the reformed gas addition device 12, and the urea water addition device 5 are controlled by the control device 13 via a control signal 13a. It has become so.

尚、図1中における制御信号13aは説明の便宜上から燃料添加装置10と改質ガス添加装置12及び尿素水添加装置5の夫々に向かって直接的に延びているが、実際には、これらの作動を担う機器類への電気信号として出力されることは勿論である。   The control signal 13a in FIG. 1 extends directly toward the fuel addition device 10, the reformed gas addition device 12, and the urea water addition device 5 for convenience of explanation. Of course, it is output as an electrical signal to the equipment responsible for the operation.

ここで、前記酸化触媒9の出側には、該酸化触媒9の温度の代用値として排気ガス1の温度を検出する温度センサ14が配置されていると共に、前記選択還元型触媒3の入側には、該選択還元型触媒3の温度の代用値として排気ガス1の温度を検出する温度センサ15が配置されており、これらの温度センサ14,15の検出信号14a,15aが前記制御装置13に入力されるようになっている。   Here, a temperature sensor 14 for detecting the temperature of the exhaust gas 1 as a substitute value for the temperature of the oxidation catalyst 9 is disposed on the outlet side of the oxidation catalyst 9, and the inlet side of the selective catalytic reduction catalyst 3. Is provided with a temperature sensor 15 for detecting the temperature of the exhaust gas 1 as a substitute value for the temperature of the selective catalytic reduction catalyst 3, and detection signals 14 a and 15 a of these temperature sensors 14 and 15 are used as the control device 13. To be input.

前記制御装置13においては、前記温度センサ14,15の検出信号14a,15aに基づいて、前記酸化触媒9の温度が前記改質ガス添加装置12からの改質ガス11を酸化処理可能な活性下限温度を成す第一温度(約80℃程度)以上で且つ前記燃料添加装置10からの添加燃料8を酸化処理可能な活性下限温度を成す第二温度(約200℃程度)を下まわっている時に前記改質ガス添加装置12による改質ガス11の導入を実施し、前記酸化触媒9の温度が前記第二温度以上となっている時には燃料添加装置10による燃料8の直噴を実施し得るようにしてある。   In the control device 13, based on the detection signals 14 a and 15 a of the temperature sensors 14 and 15, the lower limit of the activity at which the temperature of the oxidation catalyst 9 can oxidize the reformed gas 11 from the reformed gas addition device 12. When the temperature is lower than the first temperature (about 80 ° C.) that is higher than the first temperature (about 80 ° C.) and lower than the second temperature (about 200 ° C.) that constitutes the lower limit temperature of activation of the added fuel 8 from the fuel addition device 10 When the reformed gas 11 is introduced by the reformed gas adding device 12 and the temperature of the oxidation catalyst 9 is equal to or higher than the second temperature, the fuel adding device 10 can directly inject the fuel 8. It is.

また、図2を用いて前記改質ガス添加装置12の具体的な構造につき補足しておくと、この改質ガス添加装置12は、燃料8をH2とCOに分解する性質を備えた通気構造の改質触媒16と、該改質触媒16を収容して一端側を排気管2内に開放したケーシング17と、該ケーシング17の他端側に接続されて改質ガス11を一端側へ掃気するための搬送空気18を導く搬送空気供給管19と、前記ケーシング17の他端側に接続されて燃料8を前記改質触媒16に供給する燃料供給管20と、前記改質触媒16を加熱するグロープラグ21(加熱手段)とを備えて構成されている。 Further, with reference to FIG. 2, the specific structure of the reformed gas addition device 12 will be supplemented. This reformed gas addition device 12 is a vent having the property of decomposing the fuel 8 into H 2 and CO. A reforming catalyst 16 having a structure, a casing 17 containing the reforming catalyst 16 and having one end opened into the exhaust pipe 2, and connected to the other end of the casing 17 to connect the reformed gas 11 to one end. A carrier air supply pipe 19 that guides the carrier air 18 for scavenging, a fuel supply pipe 20 that is connected to the other end of the casing 17 and supplies the fuel 8 to the reforming catalyst 16, and the reforming catalyst 16 A glow plug 21 (heating means) for heating is provided.

ここで、前記通気構造の改質触媒16は、例えば、金属メッシュに触媒原料をコーティングして構成することが可能であり、ここに適宜数のグロープラグ21をケーシング17の他端側から挿し込むようにして配置し、前記各グロープラグ21に対し通電して発熱させることで前記改質触媒16を昇温し得るようになっている。   Here, the reforming catalyst 16 having the ventilation structure can be configured by coating a metal mesh with a catalyst raw material, for example, and an appropriate number of glow plugs 21 are inserted into the casing 17 from the other end side. The reforming catalyst 16 can be heated by energizing each glow plug 21 to generate heat.

斯かる改質ガス添加装置12で排気管2内に改質ガス11を導入するにあたっては、グロープラグ21により改質触媒16を加熱して触媒活性を高めた上、該改質触媒16に燃料供給管20から燃料8を供給し且つケーシング17の他端側に搬送空気供給管19から搬送空気18を導くと、前記改質触媒16にて燃料8が反応性の高い改質ガス11に分解されて搬送空気18により排気管2内に送り出されることになる。   When the reformed gas 11 is introduced into the exhaust pipe 2 by the reformed gas addition device 12, the reforming catalyst 16 is heated by the glow plug 21 to increase the catalytic activity, and the reforming catalyst 16 is supplied with fuel. When the fuel 8 is supplied from the supply pipe 20 and the carrier air 18 is guided from the carrier air supply pipe 19 to the other end side of the casing 17, the fuel 8 is decomposed into a highly reactive reformed gas 11 by the reforming catalyst 16. Then, it is sent out into the exhaust pipe 2 by the carrier air 18.

而して、このように排気浄化装置を構成すれば、図3のグラフ中に曲線Aで示す通り、酸化触媒9の温度が添加燃料8を酸化処理可能な第二温度(約200℃程度)を下まわっていても、該第二温度より低い第一温度(約80℃程度)に達した段階T1で改質ガス添加装置12による改質ガス11の導入が実施され、その下流に配置されている酸化触媒9にて反応性の高い改質ガス11が酸化処理され、その反応熱により前記酸化触媒9が急速に昇温して第二温度に達し、この段階T2で改質ガス添加装置12による改質ガス11の導入から燃料添加装置10による燃料8の排気管2内への直噴に切り替わり、活性の上がった酸化触媒9にて添加燃料8が直接的に酸化処理され、その反応熱で加熱された排気ガス1が更に下流の選択還元型触媒3を通過することで該選択還元型触媒3が従来より早期に昇温されることになる(改質ガス11の先行導入がなければ曲線Bのように前記段階T2より遅い段階T3まで燃料8の添加を開始できない)。 Thus, when the exhaust gas purification apparatus is configured in this way, as shown by the curve A in the graph of FIG. 3, the temperature of the oxidation catalyst 9 is the second temperature (about 200 ° C.) at which the added fuel 8 can be oxidized. However, the reformed gas addition device 12 introduces the reformed gas 11 at the stage T 1 when the temperature reaches a first temperature (about 80 ° C.) lower than the second temperature, and is disposed downstream of the first temperature. The reformed gas 11 having high reactivity is oxidized by the oxidation catalyst 9 and the temperature of the oxidation catalyst 9 is rapidly raised by the reaction heat to reach the second temperature. At this stage T 2 , the reformed gas The introduction of the reformed gas 11 by the addition device 12 is switched to the direct injection of the fuel 8 into the exhaust pipe 2 by the fuel addition device 10, and the added fuel 8 is directly oxidized by the oxidation catalyst 9 having increased activity, The exhaust gas 1 heated by the reaction heat is further selectively reduced downstream. 3, the temperature of the selective catalytic reduction catalyst 3 is raised earlier than before (if there is no prior introduction of the reformed gas 11, until the stage T 3 that is later than the stage T 2 as shown by the curve B). The addition of fuel 8 cannot be started).

従って、本形態例によれば、酸化触媒9の温度が添加燃料8を酸化処理可能な第二温度を下まわっている時に、該第二温度より低い第一温度に達した段階から改質ガス添加装置12による改質ガス11の導入を実施し、該改質ガス11を下流の酸化触媒9で酸化処理させることにより該酸化触媒9を反応熱で急速に昇温して第二温度まで到達させることができ、これ以降は、改質ガス添加装置12による改質ガス11の導入から燃料添加装置10による燃料8の排気管2内への直噴に切り替えることによって、活性の上がった酸化触媒9にて添加燃料8を直接的に酸化処理することで燃料8の発熱量を最大限に利用して排気ガス1を加熱し、該排気ガス1を更に下流の選択還元型触媒3を通過させることで該選択還元型触媒3を従来より早期に昇温させることができ、該選択還元型触媒3を冷機始動時でも早期に活性化させて尿素水4の添加を従来より早い段階から開始することができ、冷機始動時におけるNOx低減率の大幅な向上を図ることができる。   Therefore, according to the present embodiment, when the temperature of the oxidation catalyst 9 is lower than the second temperature at which the added fuel 8 can be oxidized, the reformed gas starts from the stage where the first temperature lower than the second temperature is reached. The reforming gas 11 is introduced by the adding device 12, and the reforming gas 11 is oxidized with the downstream oxidation catalyst 9, whereby the oxidation catalyst 9 is rapidly heated with the reaction heat to reach the second temperature. Thereafter, by switching from the introduction of the reformed gas 11 by the reformed gas adding device 12 to the direct injection of the fuel 8 into the exhaust pipe 2 by the fuel adding device 10, the oxidation catalyst with increased activity is obtained. 9, by directly oxidizing the added fuel 8, the exhaust gas 1 is heated using the maximum amount of heat generated by the fuel 8, and the exhaust gas 1 passes through the selective catalytic reduction catalyst 3 further downstream. Therefore, the selective catalytic reduction catalyst 3 is made earlier than before. The temperature can be raised, and the selective catalytic reduction catalyst 3 can be activated at an early stage even at the time of cold start so that the addition of the urea water 4 can be started from an earlier stage than before, and the NOx reduction rate at the cold start is greatly increased. Can be improved.

ここで、補足して説明しておくと、燃料8は改質触媒16で改質ガス11に分解されることで既にエネルギーロスを生じてしまうので、改質ガス添加装置12による改質ガス11の導入だけで選択還元型触媒3の昇温を図るのは効率が悪く、できるだけ早く燃料添加装置10による燃料8の排気管2内への直噴に切り替えて燃料8の発熱量を最大限に利用することが重要である。   Here, as a supplementary explanation, since the fuel 8 is already decomposed into the reformed gas 11 by the reforming catalyst 16, energy loss has already occurred. It is not efficient to raise the temperature of the selective catalytic reduction catalyst 3 only by introducing the fuel, and the direct addition of the fuel 8 into the exhaust pipe 2 by the fuel addition device 10 is switched as soon as possible to maximize the heat generation amount of the fuel 8. It is important to use it.

また、ここに図示している例では、選択還元型触媒3の上流側にパティキュレートフィルタ7が備えられているが、該パティキュレートフィルタ7の強制再生を行う際にも、前述の燃料添加装置10と改質ガス添加装置12の切り替え制御を流用することによって、パティキュレートフィルタ7を排気温度の低い運転条件下でも早期にパティキュレート(煤分)を燃焼除去し得る再生温度まで到達させることができ、パティキュレートフィルタ7の再生時間の大幅な短縮を図ることができる。   Further, in the example shown here, the particulate filter 7 is provided on the upstream side of the selective catalytic reduction catalyst 3. However, when the particulate filter 7 is forcibly regenerated, the above-described fuel addition device is provided. By diverting the switching control between 10 and the reformed gas addition device 12, the particulate filter 7 can reach a regeneration temperature at which particulates (prorated) can be burned and removed at an early stage even under operating conditions with a low exhaust temperature. Thus, the regeneration time of the particulate filter 7 can be greatly shortened.

尚、パティキュレートフィルタ7の強制再生を行うに際しては、図示しないエンジンにおいて、圧縮上死点付近で行われる燃料のメイン噴射に続いて圧縮上死点より遅い非着火のタイミングでポスト噴射を追加することで排気ガス1中に燃料を添加するのが一般的で、ポスト噴射が使用できる温度になるまで時間がかかるという課題や、エンジン側と独立して燃料添加量を制御することができないために温度コントロールが難しいという課題があったが、これらの課題を払拭できるというメリットもある。   When the particulate filter 7 is forcibly regenerated, post-injection is added at a non-ignition timing later than the compression top dead center in the engine (not shown) following the main injection of fuel performed near the compression top dead center. Therefore, it is common to add fuel to the exhaust gas 1, because it takes time to reach a temperature at which post injection can be used, and the amount of fuel added cannot be controlled independently of the engine side. There is a problem that temperature control is difficult, but there is also an advantage that these problems can be eliminated.

また、図4は本発明の別の形態例を示すもので、本形態例においては、改質ガス添加装置12に、改質ガス11に着火するための着火手段としてグロープラグ22をケーシング17の一端側のガス出口部17aに配置すると共に、改質ガス11の燃焼を助勢する燃焼空気23を導く燃焼空気供給管24を前記ケーシング17内におけるグロープラグ22の直前位置に接続した構成を採用しており、前述の燃料添加装置10と改質ガス添加装置12の切り替え制御に加え、酸化触媒9の温度が第一温度を下まわっている時に改質ガス添加装置12により改質ガス11を生成し且つ該改質ガス11に着火してバーナ燃焼を実施し得るようになっている。   FIG. 4 shows another embodiment of the present invention. In this embodiment, the reformed gas adding device 12 is provided with a glow plug 22 as an ignition means for igniting the reformed gas 11. A configuration in which a combustion air supply pipe 24 that guides combustion air 23 that assists combustion of the reformed gas 11 is connected to a position immediately before the glow plug 22 in the casing 17 is disposed at the gas outlet portion 17a on one end side. In addition to the switching control between the fuel addition device 10 and the reformed gas addition device 12 described above, the reformed gas 11 is generated by the reformed gas addition device 12 when the temperature of the oxidation catalyst 9 is lower than the first temperature. In addition, the reformed gas 11 can be ignited to perform burner combustion.

このように改質ガス添加装置12を構成した場合、酸化触媒9の温度が第一温度を下まわっていても、図5のグラフ中に曲線A’で示す通り、改質ガス添加装置12により生成された改質ガス11がグロープラグ22により着火され且つ燃焼空気供給管24により燃焼空気23が供給されることでバーナ燃焼が実施されるので、該バーナ燃焼により酸化触媒9が速やかに昇温されて第一温度に達し、先の図1〜図3の形態例における段階T1(図3参照)より早い段階T1’から改質ガス添加装置12による改質ガス11の導入が開始され、先の図1〜図3の形態例における段階T2(図3参照)より早い段階T2’から燃料添加装置10による燃料8の排気管2内への直噴が開始されることになる(バーナ燃焼の実施がなく且つ改質ガス11の先行導入もなければ曲線Bのように前記段階T2’より遅い段階T3まで燃料8の添加を開始できない)。 When the reformed gas addition device 12 is configured in this way, even if the temperature of the oxidation catalyst 9 is lower than the first temperature, as shown by the curve A ′ in the graph of FIG. Since the generated reformed gas 11 is ignited by the glow plug 22 and the combustion air 23 is supplied by the combustion air supply pipe 24, the burner combustion is performed. Therefore, the oxidation catalyst 9 is quickly heated by the burner combustion. Thus, the first temperature is reached, and the introduction of the reformed gas 11 by the reformed gas addition device 12 is started from the stage T 1 ′ earlier than the stage T 1 (see FIG. 3) in the embodiment of FIGS. The direct injection of the fuel 8 into the exhaust pipe 2 by the fuel addition device 10 is started from the stage T 2 ′ earlier than the stage T 2 (see FIG. 3) in the embodiment of FIGS. (There is no burner combustion and the reformed gas 11 Line introduction can not start addition of fuel 8 even the stage T 2 later stage T 3 than 'as indicated by a curve B if).

従って、本形態例によれば、酸化触媒9の温度が第一温度を下まわっている時に、改質ガス添加装置12により生成された改質ガス11に着火手段で着火することによりバーナ燃焼を実施することができ、該バーナ燃焼により酸化触媒9を速やかに昇温して第一温度まで上げることができるので、改質ガス添加装置12による改質ガス11の導入の開始時期を早め、延いては燃料添加装置10による燃料8の排気管2内への直噴への切り替え時期を早めることができるので、選択還元型触媒3をより一層速やかに昇温して更に早期な活性化を図ることができ、冷機始動時におけるNOx低減率の更なる向上を図ることができる。   Therefore, according to the present embodiment, burner combustion is performed by igniting the reformed gas 11 generated by the reformed gas adding device 12 by the ignition means when the temperature of the oxidation catalyst 9 is lower than the first temperature. The oxidation catalyst 9 can be quickly heated up to the first temperature by the burner combustion, so that the start timing of the introduction of the reformed gas 11 by the reformed gas addition device 12 can be advanced and extended. In this case, the timing for switching the fuel 8 to the direct injection of the fuel 8 into the exhaust pipe 2 can be advanced, so that the temperature of the selective catalytic reduction catalyst 3 can be increased more quickly to achieve further activation. It is possible to further improve the NOx reduction rate at the time of cold start.

また、パティキュレートフィルタ7を強制再生するにあたっても、該パティキュレートフィルタ7をより一層速やかに昇温して更に早期にパティキュレート(煤分)を燃焼除去し得る再生温度まで到達させることができ、パティキュレートフィルタ7の再生時間の更に大幅な短縮を図ることができる。   Further, even when the particulate filter 7 is forcibly regenerated, the temperature of the particulate filter 7 can be increased more quickly to reach a regeneration temperature at which the particulates can be burned and removed earlier. The regeneration time of the particulate filter 7 can be further greatly shortened.

尚、本発明の排気浄化装置は、上述の形態例にのみ限定されるものではなく、本発明の要旨を逸脱しない範囲内において種々変更を加え得ることは勿論である。   Note that the exhaust emission control device of the present invention is not limited to the above-described embodiment, and it is needless to say that various modifications can be made without departing from the gist of the present invention.

2 排気管
3 選択還元型触媒(後処理装置)
7 パティキュレートフィルタ(後処理装置)
8 燃料
9 酸化触媒
10 燃料添加装置(燃料添加手段)
11 改質ガス
12 改質ガス添加装置(改質ガス添加手段)
16 改質触媒
17 ケーシング
18 搬送空気
19 搬送空気供給管
20 燃料供給管
21 グロープラグ(加熱手段)
22 グロープラグ(着火手段)
23 燃焼空気
24 燃焼空気供給管
2 Exhaust pipe 3 Selective reduction catalyst (post-processing equipment)
7 Particulate filter (post-processing device)
8 Fuel 9 Oxidation catalyst 10 Fuel addition device (fuel addition means)
11 Reformed gas 12 Reformed gas addition device (reformed gas addition means)
16 reforming catalyst 17 casing 18 carrier air 19 carrier air supply pipe 20 fuel supply pipe 21 glow plug (heating means)
22 Glow plug (ignition means)
23 Combustion air 24 Combustion air supply pipe

Claims (3)

排気管途中の後処理装置より上流に酸化触媒を備え、該酸化触媒に対し燃料を添加して該燃料が前記酸化触媒上で酸化反応した時の反応熱により前記後処理装置の昇温を図り得るようにした排気浄化装置であって、前記酸化触媒より上流の排気管に、燃料を排気管内に直噴する燃料添加手段と、燃料を反応性の高い改質ガスに分解して排気管内に導入する改質ガス添加手段とを備え、前記酸化触媒の温度が前記改質ガス添加手段からの改質ガスを酸化処理可能な活性下限温度を成す第一温度以上で且つ前記燃料添加手段からの添加燃料を酸化処理可能な活性下限温度を成す第二温度を下まわっている時に前記改質ガス添加手段による改質ガスの導入を実施し、前記酸化触媒の温度が前記第二温度以上となっている時には燃料添加手段による燃料の直噴を実施し得るように構成したことを特徴とする排気浄化装置。   An oxidation catalyst is provided upstream of the aftertreatment device in the middle of the exhaust pipe, and fuel is added to the oxidation catalyst, and the temperature of the aftertreatment device is increased by reaction heat when the fuel undergoes an oxidation reaction on the oxidation catalyst. An exhaust gas purification apparatus configured to obtain a fuel addition means for directly injecting fuel into an exhaust pipe upstream of the oxidation catalyst, and decomposing the fuel into a highly reformed reformed gas into the exhaust pipe. A reformed gas adding means to be introduced, wherein the temperature of the oxidation catalyst is equal to or higher than a first temperature that constitutes an activation lower limit temperature at which the reformed gas from the reformed gas adding means can be oxidized, and from the fuel adding means. When the reformed gas is introduced by the reformed gas adding means when the temperature is lower than the second temperature that is the minimum active temperature at which the added fuel can be oxidized, the temperature of the oxidation catalyst becomes equal to or higher than the second temperature. When fuel is added Exhaust gas purification apparatus characterized by being configured so as to implement the direct injection of. 前記改質ガス添加手段が、燃料を反応性の高い改質ガスに分解する性質を備えた通気構造の改質触媒と、該改質触媒を収容して一端側を排気管内に開放したケーシングと、該ケーシングの他端側に接続されて改質ガスを一端側へ掃気するための搬送空気を導く搬送空気供給管と、前記ケーシングの他端側に接続されて燃料を前記改質触媒に供給する燃料供給管と、前記改質触媒を加熱する加熱手段とを備えていることを特徴とする請求項1に記載の排気浄化装置。   A reforming catalyst having a ventilation structure in which the reformed gas adding means has a property of decomposing fuel into a highly reactive reformed gas; and a casing containing the reforming catalyst and having one end opened in the exhaust pipe; A carrier air supply pipe connected to the other end side of the casing to guide the carrier air for scavenging the reformed gas to one end side, and connected to the other end side of the casing to supply fuel to the reforming catalyst The exhaust emission control device according to claim 1, further comprising a fuel supply pipe that performs heating and a heating unit that heats the reforming catalyst. 前記改質ガス添加手段が、改質ガスに着火するための着火手段と、改質ガスの燃焼を助勢する燃焼空気を導く燃焼空気供給管とを備え、酸化触媒の温度が第一温度を下まわっている時に改質ガス添加手段により改質ガスを生成し且つ該改質ガスに着火してバーナ燃焼を実施し得るように構成されていることを特徴とする請求項1又は2に記載の排気浄化装置。   The reformed gas adding means includes an ignition means for igniting the reformed gas, and a combustion air supply pipe for guiding combustion air for assisting combustion of the reformed gas, and the temperature of the oxidation catalyst falls below the first temperature. 3. The burner combustion can be performed by generating a reformed gas by the reformed gas addition means when turning and igniting the reformed gas. 4. Exhaust purification device.
JP2012136761A 2012-06-18 2012-06-18 Exhaust purification device Active JP6005413B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2012136761A JP6005413B2 (en) 2012-06-18 2012-06-18 Exhaust purification device

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2012136761A JP6005413B2 (en) 2012-06-18 2012-06-18 Exhaust purification device

Publications (2)

Publication Number Publication Date
JP2014001664A true JP2014001664A (en) 2014-01-09
JP6005413B2 JP6005413B2 (en) 2016-10-12

Family

ID=50035069

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2012136761A Active JP6005413B2 (en) 2012-06-18 2012-06-18 Exhaust purification device

Country Status (1)

Country Link
JP (1) JP6005413B2 (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2015190369A (en) * 2014-03-28 2015-11-02 株式会社クボタ Exhaust treatment device of engine
JP2016008535A (en) * 2014-06-24 2016-01-18 株式会社クボタ Engine exhaust treatment device
JP2017008801A (en) * 2015-06-22 2017-01-12 株式会社クボタ Exhaust treatment device of engine
WO2018080179A1 (en) * 2016-10-26 2018-05-03 두산인프라코어 주식회사 Exhaust gas post-processing system
US10619553B2 (en) 2017-03-30 2020-04-14 Subaru Corporation Engine-controlling device

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN207363744U (en) * 2017-02-08 2018-05-15 天纳克(苏州)排放系统有限公司 Heating and filtering component and after-treatment system component
CN207470267U (en) * 2017-02-08 2018-06-08 天纳克(苏州)排放系统有限公司 Urea filtration system and after-treatment system component

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0633748A (en) * 1992-07-10 1994-02-08 Aisin Seiki Co Ltd On-vehicle hydrogen supplier
JP2010031858A (en) * 2008-07-15 2010-02-12 Friedrich Boysen Gmbh & Co Kg Regenerating device
JP2010077916A (en) * 2008-09-26 2010-04-08 Hitachi Constr Mach Co Ltd Exhaust emission control device
JP2010248943A (en) * 2009-04-13 2010-11-04 Isuzu Motors Ltd Exhaust gas temperature raising device

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0633748A (en) * 1992-07-10 1994-02-08 Aisin Seiki Co Ltd On-vehicle hydrogen supplier
JP2010031858A (en) * 2008-07-15 2010-02-12 Friedrich Boysen Gmbh & Co Kg Regenerating device
JP2010077916A (en) * 2008-09-26 2010-04-08 Hitachi Constr Mach Co Ltd Exhaust emission control device
JP2010248943A (en) * 2009-04-13 2010-11-04 Isuzu Motors Ltd Exhaust gas temperature raising device

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2015190369A (en) * 2014-03-28 2015-11-02 株式会社クボタ Exhaust treatment device of engine
JP2016008535A (en) * 2014-06-24 2016-01-18 株式会社クボタ Engine exhaust treatment device
JP2017008801A (en) * 2015-06-22 2017-01-12 株式会社クボタ Exhaust treatment device of engine
WO2018080179A1 (en) * 2016-10-26 2018-05-03 두산인프라코어 주식회사 Exhaust gas post-processing system
CN109891064A (en) * 2016-10-26 2019-06-14 斗山英维高株式会社 Exhausted gas post-processing system
US11041419B2 (en) 2016-10-26 2021-06-22 Doosan Infracore Co., Ltd. Exhaust gas post-processing system
CN109891064B (en) * 2016-10-26 2021-10-01 斗山英维高株式会社 Exhaust gas aftertreatment system
US10619553B2 (en) 2017-03-30 2020-04-14 Subaru Corporation Engine-controlling device

Also Published As

Publication number Publication date
JP6005413B2 (en) 2016-10-12

Similar Documents

Publication Publication Date Title
JP6005413B2 (en) Exhaust purification device
KR100922513B1 (en) Exhaust aftertreatment system and method for lean burn internal combustion engines
JP5449009B2 (en) Exhaust purification device
JP5846488B2 (en) Exhaust gas purification device for internal combustion engine
JP2012525540A (en) Diesel aftertreatment system
JP2009091909A (en) Exhaust emission control device
JP2008196328A (en) Exhaust emission control device
KR20130003980A (en) System for purifying exhaust gas and exhaust system having the same
KR20130087146A (en) Apparatus and controlling method of urea-scr system
KR100999616B1 (en) Apparatus for reducing nitrogen oxide cotained in exhaust gas
JP2009114930A (en) Exhaust purification device
RU2011134878A (en) DEVICE AND METHOD FOR REGENERATING A FILTER OF SOLID PARTICLES LOCATED IN THE EXHAUST GAS LINE OF THE INTERNAL COMBUSTION ENGINE
JP5316266B2 (en) Reducing agent supply device for urea SCR catalyst
JP2008274850A (en) Exhaust emission control device
KR102517484B1 (en) Methods and Systems for Removal of Toxic Compounds from Engine Exhaust Gas
JP5609175B2 (en) Exhaust gas purification method and apparatus
JP2010248955A (en) Exhaust emission control device
JP2014185575A (en) Exhaust emission control device for internal combustion engine
JP2005273614A (en) Urea water adding device
CN113833552B (en) Carbon particle removal method and exhaust gas aftertreatment system
JP2014015909A (en) Exhaust emission control device
KR102154368B1 (en) Selective Catalytic Reduction System for Engine
JP2005002925A (en) Exhaust emission control device
JP6119426B2 (en) Urea SCR system
JP7280169B2 (en) Exhaust purification device

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20150525

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20160120

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20160126

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20160316

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20160830

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20160907

R150 Certificate of patent or registration of utility model

Ref document number: 6005413

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R150

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250