JP2845080B2 - Exhaust gas purification device for internal combustion engine - Google Patents
Exhaust gas purification device for internal combustion engineInfo
- Publication number
- JP2845080B2 JP2845080B2 JP5741293A JP5741293A JP2845080B2 JP 2845080 B2 JP2845080 B2 JP 2845080B2 JP 5741293 A JP5741293 A JP 5741293A JP 5741293 A JP5741293 A JP 5741293A JP 2845080 B2 JP2845080 B2 JP 2845080B2
- Authority
- JP
- Japan
- Prior art keywords
- absorbent
- exhaust
- exhaust gas
- air
- fuel ratio
- 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 - Lifetime
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- Exhaust Gas After Treatment (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明は、内燃機関の排気浄化装
置に関し、詳細には、ディーゼルエンジンや希薄燃焼を
行うガソリンエンジン等、リーン空燃比の燃焼を行う内
燃機関の排気中のNOX を効果的に除去可能な排気浄化
装置に関する。BACKGROUND OF THE INVENTION The present invention relates to an exhaust purifying apparatus for an internal combustion engine, in particular, a gasoline engine or the like for a diesel engine or lean burn, the NO X in the exhaust gas of an internal combustion engine causing combustion of lean air-fuel ratio The present invention relates to an exhaust purification device that can be removed effectively.
【0002】[0002]
【従来の技術】この種の排気浄化装置の例としては、例
えば特開昭62─106826号公報に開示されたもの
がある。同公報の装置は、ディーゼル機関の排気通路に
酸素の存在下でNOX を吸収する吸収剤(触媒)を配置
して排気中のNOX を吸収させ、該吸収剤のNOX 吸収
能力が飽和したときに吸収剤への排気の流入を遮断して
吸収剤に還元剤を供給し、吸収剤からNOX を放出させ
るとともに放出されたNOX を還元浄化するようにした
ものである。2. Description of the Related Art An example of this type of exhaust gas purifying apparatus is disclosed, for example, in Japanese Patent Application Laid-Open No. 62-106826. The apparatus of this publication is to place the absorbent to absorb NO X in the presence of oxygen in an exhaust passage of a diesel engine (catalyst) to absorb the NO X in the exhaust gas, NO X absorption ability of the absorbent is saturated to shut off the flow of exhaust gas into the absorbent supplying reducing agent to the absorbent when the is the NO X released with the release of NO X from the absorbent that so as to reduce and purify.
【0003】[0003]
【発明が解決しようとする課題】上記特開昭62─10
6826号公報の排気浄化装置では、NOX 吸収剤から
のNOX の放出と還元浄化(以下「再生」という)を行
うために、水素等の気体状還元剤をNOX 吸収剤に供給
し、NOX 吸収剤をリッチ空燃比下の雰囲気にすること
によりNOX の再生を行っている。Problems to be Solved by the Invention
In the exhaust purification device disclosed in Japanese Patent No. 6826, a gaseous reducing agent such as hydrogen is supplied to the NO X absorbent in order to release NO X from the NO X absorbent and perform reduction purification (hereinafter referred to as “regeneration”). It is performed regeneration of the NO X by the the NO X absorbent in an atmosphere under a rich air-fuel ratio.
【0004】しかし、上記公報の装置ではNOX 吸収剤
の再生操作時に、還元剤の供給を開始してからNOX 吸
収剤の雰囲気がリーンからリッチに切り換わるのに時間
がかかるような場合には、NOX 吸収剤上での還元剤の
燃焼によりNOX 吸収剤の温度が上昇し、リッチ雰囲気
に切り換わる前にNOX 吸収剤からNOX が放出されて
しまう場合がある。この時、NOX 吸収剤は十分な還元
雰囲気(リッチ雰囲気)にないため、放出されたNOX
は十分に還元されず未浄化のNOX が大気に放出されて
しまう場合がある。However, during the regenerating operation of the NO X absorbent in the apparatus of the above publication, when the atmosphere of the NO X absorbent from the start of the supply of the reducing agent, such as take time to switch from lean to rich is elevated temperature of the NO X absorbent by the combustion of the reducing agent on the NO X absorbent, there is a case where NO X from the NO X absorbent before switching to rich atmosphere from being released. At this time, since the NO X absorbent is not in a sufficient reducing atmosphere (rich atmosphere), the released NO X
May not be sufficiently reduced and unpurified NO X may be released to the atmosphere.
【0005】また、この未浄化のNOX の大気放出を防
止するためには、多量の還元剤を供給して短時間でNO
X 吸収剤の雰囲気をリッチに切り換える必要があるが、
この場合再生時のNOX 吸収剤の雰囲気がリッチになり
すぎて(空燃比が低くなりすぎて)、NOX 吸収剤から
放出されたNOX の一部が過剰なHC成分と反応してア
ンモニア(NH3 )を生成し、このアンモニアが大気に
放出されてしまう問題が生じる。In order to prevent the unpurified NO X from being released into the atmosphere, a large amount of a reducing agent is supplied and NO
It is necessary to switch the atmosphere of X absorbent richly,
In this case the atmosphere of the NO X absorbent during regeneration becomes too rich (air-fuel ratio is too low), the ammonia reacts part of the NO X released from the NO X absorbent is an excess of HC components (NH 3 ) is produced, and this ammonia is released to the atmosphere.
【0006】一方、後述のように、NOX 吸収剤の再生
操作時においては一般にNOX 吸収剤の雰囲気空燃比が
リッチなほど(すなわち空燃比が低いほど)短時間で完
全な再生を行うことができることが知られている。従っ
て、車両用の排気浄化装置等においては、できるだけ短
時間でNOX 吸収剤の再生操作を完了し、次のNOX吸
収に備えるためには還元剤の供給量を増やしてできるだ
けリッチ雰囲気下でNOX 吸収剤の再生を行うことが好
ましい。On the other hand, as described below, generally in the NO X atmosphere air-fuel ratio of the absorbent enough rich (i.e. the lower the air-fuel ratio) in a short time by performing complete regeneration at the time of regenerating operation of the NO X absorbent It is known that can be. Therefore, in the exhaust purification apparatus and the like for a vehicle, to complete the shortest possible time in the reproduction operation of the NO X absorbent, under possible rich atmosphere by increasing the supply amount of the reducing agent in order to prepare for the next of the NO X absorbent it is preferred to carry out the regeneration of the NO X absorbent.
【0007】しかし、上記公報の装置では、未浄化のN
OX やアンモニアの大気放出を防止するために還元剤の
供給量等の再生条件が制限されてしまい、短時間で効率
的なNOX 吸収剤の再生操作を行うことができない問題
が生じる。本発明は、NOX 吸収剤再生操作時の未浄化
のNOX やアンモニアの大気放出の問題を解決し、NO
X 吸収剤の再生条件の範囲を拡げて短時間で効率的なN
O X 吸収剤再生を行うことができる内燃機関の排気浄化
装置を提供することを目的としている。However, in the apparatus disclosed in the above publication, unpurified N
OXOf reducing agent to prevent atmospheric release of ammonia and ammonia
Regeneration conditions such as supply amount are limited, and efficiency is reduced in a short time
Typical NOXThe problem of not being able to perform absorbent regeneration
Occurs. The present invention provides NOXNot purified during absorbent regeneration operation
NOXTo solve the problem of atmospheric release of ammonia and ammonia
XEfficient N in a short time by expanding the range of absorbent regeneration conditions
O XExhaust purification of internal combustion engine that can perform absorbent regeneration
It is intended to provide a device.
【0008】[0008]
【課題を解決するための手段】本発明によれば、リーン
空燃比の燃焼を行うことのできる内燃機関の排気通路
に、流入排気の空燃比がリーンのときにNOX を吸収し
流入排気の酸素濃度が低下したときに吸収したNOX を
放出するNOX 吸収剤を配置して排気中のNOXを吸収
させ、その後NOX 吸収剤に流入する排気空燃比をリッ
チにして吸収したNOX をNOX 吸収剤から放出させる
と共に該NOX を還元浄化する内燃機関の排気浄化装置
において、前記NOX 吸収剤の下流側にリーン排気空燃
比条件下で排気中のNOX を還元剤と選択的に反応させ
得るNOX 選択還元触媒と、前記NO X 吸収剤に流入す
る排気空燃比をリッチにして吸収したNO X を放出させ
るときに前記NO X 選択還元触媒に流入する排気の空燃
比をリーンに維持する手段とを設けたことを特徴とする
内燃機関の排気浄化装置が提供される。According to the present invention SUMMARY OF], in an exhaust passage of an internal combustion engine capable of performing combustion of the lean air-fuel ratio, the air-fuel ratio of the inflowing exhaust is absorbed inflowing exhaust the NO X when the lean oxygen concentration to release the absorbed NO X when the reduced NO X in the absorbent arranged to absorb the NO X in the exhaust gas, then NO X exhaust air-fuel ratio flowing into the absorbent and absorbed in the rich NO X in the exhaust purification system of an internal combustion engine to reduce and purify the NO X with be released from the NO X absorbent and selective reducing agent to NO X in the exhaust gas in the lean exhaust air-fuel ratio conditions downstream of the the NO X absorbent and the NO X selective reducing catalyst capable to be reacted, to flow into the the NO X absorbent
The exhaust air-fuel ratio to release NO X absorbed in the rich that
Air-fuel of the exhaust gas flowing into the the NO X selective reducing catalyst Rutoki
Means for maintaining the ratio at a lean ratio .
【0009】[0009]
【作用】NOX 吸収剤再生操作時に発生する未浄化のN
OX やアンモニアはNOX 吸収剤下流側に配置した選択
還元触媒により同時に分解されてN2 、H2 O、CO2
に変換されるため、NOX とアンモニアが大気放出され
ることがない。[Action] the NO X absorbent unpurified generated during the regenerating operation N
O X and ammonia are simultaneously decomposed by selective reduction catalyst arranged in the NO X absorbent downstream N 2, H 2 O, CO 2
NO X and ammonia are not released to the atmosphere.
【0010】[0010]
【実施例】以下、添付図面を用いて本発明の実施例を説
明する。図1において、1は図示しない内燃機関の排気
管を示す。本実施例では排気管1には2つの分岐通路3
a、3bが設けられており、通路3a側には上流側か
ら、後述する還元剤供給装置11とNOX 吸収剤5、及
び排気温度に応じた信号を発生する排気温度センサ6、
排気中の酸素濃度に対応する連続出力を発生する酸素濃
度センサ7がそれぞれ設けられている。また、排気通路
3bは排気温度センサ6と酸素濃度センサ7の下流側で
再び排気通路3aと合流している。すなわち、排気通路
3bは、NOX 吸収剤5をバイパスして排気を下流側に
流すバイパス通路の役割を果たしている。Embodiments of the present invention will be described below with reference to the accompanying drawings. In FIG. 1, reference numeral 1 denotes an exhaust pipe of an internal combustion engine (not shown). In this embodiment, the exhaust pipe 1 has two branch passages 3.
a, 3b are provided, the exhaust gas temperature sensor 6 in the passage 3a from upstream, for generating a signal corresponding to the later-described reducing agent supply device 11 and the NO X absorbent 5, and the exhaust temperature,
An oxygen concentration sensor 7 that generates a continuous output corresponding to the oxygen concentration in the exhaust gas is provided. The exhaust passage 3b joins the exhaust passage 3a again downstream of the exhaust gas temperature sensor 6 and the oxygen concentration sensor 7. That is, the exhaust passage 3b plays a role of a bypass passage for flowing the exhaust to bypass the the NO X absorbent 5 on the downstream side.
【0011】更に、排気管1の排気通路3a、3bの分
岐部には排気切り換え弁2が設けられ、排気通路3a、
3bの一方を所定の開度に閉鎖して排気通路3a、3b
に排気を分配するようになっている。図に2aで示すの
は、後述するエンジン制御回路(ECU)20からの制
御信号により切り換え弁2を駆動して所定の切り換え位
置をとらせるための負圧アクチュエータ等、適宜な形式
のアクチュエータである。Further, an exhaust switching valve 2 is provided at a branch portion of the exhaust passages 3a and 3b of the exhaust pipe 1, and the exhaust passage 3a
One of the exhaust passages 3a and 3b is closed to a predetermined opening degree.
The exhaust is distributed to the An actuator of an appropriate type, such as a negative pressure actuator for driving the switching valve 2 to a predetermined switching position by driving a switching valve 2 by a control signal from an engine control circuit (ECU) 20 to be described later, is shown in FIG. .
【0012】本実施例では、NOX 吸収剤5の下流側の
排気通路3a、3bの合流部の更に下流の排気管1には
後述するNOX 選択還元触媒9が設けられている。すな
わち、NOX 選択触媒9には排気通路3aと3bの両方
を通る排気が流入するようになっている。図に20で示
すのはエンジン1の制御回路(ECU)である。ECU
20はCPU、RAM、ROM、及び入力ポート、出力
ポートを相互に双方向バスで接続した構成の公知のディ
ジタルコンピュータからなり、エンジンの燃料噴射量制
御等の基本制御を行っている。また、本実施例ではEC
U20は、更に、図示しない駆動回路や負圧制御弁等を
介してアクチュエータ2aを駆動して排気切り換え弁2
の切り換え位置制御を行うほか、還元剤供給装置11か
らの還元剤供給制御を行っている。これらの制御のため
ECU20の入力ポートには、排気温度、排気酸素濃度
が、排気温度センサ6及び酸素濃度センサ7からそれぞ
れ入力されているほか、エンジン回転数、アクセル開度
等の信号がそれぞれ図示しないセンサから入力されてい
る。[0012] In this embodiment, the downstream side of the exhaust passage 3a of the NO X absorbent 5, NO X selective reduction catalyst 9 further described below in the exhaust pipe 1 downstream of the merging portion of 3b is provided. That is, the exhaust gas flowing through both the exhaust passages 3a and 3b flows into the NO X selection catalyst 9. In the figure, reference numeral 20 denotes a control circuit (ECU) of the engine 1. ECU
Reference numeral 20 denotes a known digital computer having a configuration in which a CPU, a RAM, a ROM, an input port, and an output port are connected to each other via a bidirectional bus, and performs basic control such as fuel injection amount control of an engine. In this embodiment, the EC
U20 further drives the actuator 2a via a drive circuit (not shown), a negative pressure control valve, and the like to drive the exhaust switching valve 2
In addition to performing the switching position control, the reducing agent supply control from the reducing agent supply device 11 is performed. For these controls, the input ports of the ECU 20 are supplied with the exhaust gas temperature and the exhaust oxygen concentration from the exhaust gas temperature sensor 6 and the oxygen concentration sensor 7, respectively, and also show signals such as the engine speed and the accelerator opening, respectively. Not input from sensor.
【0013】還元剤供給装置11は排気通路3aのNO
X 吸収剤5上流側に後述の還元剤を供給する噴射弁11
aを備えている。噴射弁11aはNOX 吸収剤5の再生
操作時にECU20の制御信号に応じた開度まで開弁
し、開度に応じた量の還元剤を排気通路3aに供給す
る。NOX 吸収剤5のNOX 放出、還元操作(再生操
作)に使用する還元剤としては、排気中で炭化水素、一
酸化炭素等の還元成分を発生するものであれば良く、水
素、一酸化炭素等の気体、プロパン、プロピレン、ブタ
ン等の液体又は気体の炭化水素、ガソリン、軽油、灯油
等の液体燃料等が使用できる。、本実施例では還元剤は
図示しない容器、ポンプ等の供給源から還元剤供給装置
11に供給され、ECU20の信号に応じて噴射弁11
aからNOX 吸収剤5に供給される。[0013] The reducing agent supply device 11 is connected to the NO in the exhaust passage 3a.
Injection valve 11 for supplying a reducing agent to be described later on the upstream side of X absorbent 5
a. Injector 11a is opened to the opening degree corresponding to the control signal of the ECU20 during playback operation of the NO X absorbent 5, and supplies the amount of reducing agent in accordance with the opening to the exhaust passage 3a. The NO X absorbent 5 of the NO X emission, the reducing agent used for reduction operations (playback operations), as long as it generates a hydrocarbon, reducing components such as carbon monoxide in the exhaust, hydrogen, carbon monoxide Gases such as carbon, liquid or gaseous hydrocarbons such as propane, propylene and butane, and liquid fuels such as gasoline, light oil and kerosene can be used. In the present embodiment, the reducing agent is supplied to the reducing agent supply device 11 from a supply source such as a container or a pump (not shown), and is supplied to the injection valve 11 according to a signal from the ECU 20.
a to the NO x absorbent 5.
【0014】NOX 吸収剤5は例えばアルミナ等の担体
を使用し、この担体上に例えばカリウムK,ナトリウム
Na ,リチウムLi ,セシウムCs のようなアルカリ金
属、バリウムBa , カルシウムCa のようなアルカリ土
類、ランタンLa ,イットリウムYのような希土類から
選ばれた少なくとも一つと、白金Pt のような貴金属と
が担持されている。このNOX 吸収剤5は流入する排気
の空燃比がリーンの場合にはNOX を吸収し、酸素濃度
が低下するとNOX を放出するNOX の吸放出作用を行
う。[0014] the NO X absorbent 5 uses a carrier such as alumina or the like, the carrier on, for example potassium K, sodium Na, alkali metal, barium Ba, alkaline earth such as calcium Ca, such as lithium Li, cesium Cs And at least one selected from rare earths such as lanthanum La and yttrium Y, and a noble metal such as platinum Pt. This the NO X absorbent 5 absorbs NO X in the case the air-fuel ratio of the exhaust gas flowing is lean, the oxygen concentration is carried out to absorbing and releasing action of the NO X that releases NO X when lowered.
【0015】なお、上述の排気空燃比とは、ここではN
OX 吸収剤5の上流側の排気通路やエンジン燃焼室、吸
気通路等にそれぞれ供給された空気量の合計と燃料の合
計の比を意味するものとする。従って、NOX 吸収剤5
の上流側排気通路に燃料、還元剤または空気が供給され
ない場合には排気空燃比はエンジンの運転空燃比(エン
ジン燃焼室内の燃焼における空燃比)と等しくなる。The above-mentioned exhaust air-fuel ratio is defined as N
O X absorbent upstream of 5 exhaust passage and the engine combustion chamber is intended to mean the ratio of the total sum and the fuel respectively supplied amount of air in the intake passage or the like. Therefore, NO X absorbent 5
When no fuel, reducing agent or air is supplied to the upstream exhaust passage of the engine, the exhaust air-fuel ratio becomes equal to the operating air-fuel ratio of the engine (air-fuel ratio in combustion in the engine combustion chamber).
【0016】本実施例では、リーン空燃比の燃焼を行う
機関が使用されているため、通常運転時の排気空燃比は
リーンであり、NOX 吸収剤5は排気中のNOX の吸収
を行う。また、還元剤供給装置11から排気中に還元剤
が導入されて酸素濃度が低下すると、NOX 吸収剤5は
吸収した還元剤の放出を行う。この吸放出作用の詳細な
メカニズムについては明らかでない部分もある。しか
し、この吸放出作用は図6に示すようなメカニズムで行
われているものと考えられる。次にこのメカニズムにつ
いて担体上に白金Pt およびバリウムBa を担持させた
場合を例にとって説明するが他の貴金属、アルカリ金
属、アルカリ土類、希土類を用いても同様なメカニズム
となる。In this embodiment, since an engine that performs combustion at a lean air-fuel ratio is used, the exhaust air-fuel ratio during normal operation is lean, and the NO X absorbent 5 absorbs NO X in the exhaust gas. . Also, when a reducing agent is introduced into the exhaust oxygen concentration is lowered, the release of the NO X absorbent 5 absorbs reducing agent performs a reducing agent supply device 11. The detailed mechanism of this absorption / release action is not clear in some parts. However, it is considered that this absorption / release action is performed by a mechanism as shown in FIG. Next, this mechanism will be described by taking as an example a case where platinum Pt and barium Ba are supported on a carrier, but the same mechanism can be obtained by using other noble metals, alkali metals, alkaline earths and rare earths.
【0017】すなわち、流入排気がかなりリーンになる
と流入排気中の酸素濃度が大巾に増大し、図6(A) に示
されるようにこれら酸素O2 がO2 - またはO2-の形で
白金Pt の表面に付着する。一方、流入排気中のNOは
白金Pt の表面上でこのO2 - またはO2-と反応し、N
O2 となる(2NO+O2 →2NO2 ) 。次いで生成さ
れたNO2 の一部は白金Pt上で酸化されつつ吸収剤内
に吸収されて酸化バリウムBaOと結合しながら、図6
(A) に示されるように硝酸イオンNO3 - の形で吸収剤
内に拡散する。このようにしてNOX がNOX 吸収剤5
内に吸収される。That is, the inflow exhaust gas becomes considerably lean.
And the oxygen concentration in the inflow exhaust gas greatly increased, as shown in Fig. 6 (A).
These oxygen OTwoIs OTwo -Or O2-In the form of
It adheres to the surface of platinum Pt. On the other hand, NO in the inflow exhaust gas is
This O on the surface of platinum PtTwo -Or O2-Reacts with N
OTwo(2NO + OTwo→ 2NOTwo ). Then generated
NOTwoSome of the oxygen is oxidized on platinum Pt and
FIG. 6 shows that while being absorbed by and binding to barium oxide BaO.
As shown in (A), nitrate ion NOThree -Absorbent in the form of
Spreads in. NO in this wayXIs NOXAbsorbent 5
Is absorbed into.
【0018】従って、流入排気中の酸素濃度が高い限り
白金Pt の表面でNO2 が生成され、吸収剤のNOX 吸
収能力が飽和しない限りNO2 が吸収剤内に吸収されて
硝酸イオンNO3 - が生成される。これに対して流入排
気中の酸素濃度が低下してNO2 の生成量が減少すると
反応が逆方向(NO3 - →NO2 )に進み、こうして吸
収剤内の硝酸イオンNO3 - がNO2 の形で吸収剤から
放出される。すなわち、流入排気中の酸素濃度が低下す
るとNOX 吸収剤5からNOX が放出されることにな
る。Therefore, as long as the oxygen concentration in the inflowing exhaust gas is high, NO 2 is generated on the surface of the platinum Pt, and as long as the NO x absorption capacity of the absorbent is not saturated, NO 2 is absorbed in the absorbent and nitrate ions NO 3 - is generated. On the other hand, when the oxygen concentration in the inflowing exhaust gas decreases and the amount of generated NO 2 decreases, the reaction proceeds in the reverse direction (NO 3 − → NO 2 ), and thus the nitrate ion NO 3 − in the absorbent becomes NO 2 Released from the absorbent in the form of That is, the oxygen concentration in the inflowing exhaust gas is released NO X from the NO X absorbent 5 when lowered.
【0019】一方、流入排気中にHC、CO等の還元成
分が存在すると、これらの成分は白金Pt 上の酸素O2
- またはO2-と反応して酸化され、排気中の酸素を消費
して排気中の酸素濃度を低下させる。また、排気中の酸
素濃度低下によりNOX 吸収剤5から放出されたNO2
は図6(B) に示すようにHC,COと反応して還元され
る。このようにして白金Pt の表面上にNO2 が存在し
なくなると吸収剤から次から次へとNO2 が放出され
る。On the other hand, if reducing components such as HC and CO are present in the inflowing exhaust gas, these components become oxygen O 2 on platinum Pt.
- or it is reacted with oxide and O 2-, lowering the oxygen concentration in the exhaust to consume oxygen in the exhaust. Further, the NO 2 released from the NO X absorbent 5 due to a decrease in the oxygen concentration in the exhaust gas
Is reduced by reacting with HC and CO as shown in FIG. 6 (B). When NO 2 is no longer present on the surface of the platinum Pt, NO 2 is released from the absorbent one after another.
【0020】すなわち、流入排気中のHC,COは、ま
ず白金Pt 上のO2 - またはO2-とただちに反応して酸
化され、次いで白金Pt 上のO2 - またはO2-が消費さ
れてもまだHC,COが残っていればこのHC,COに
よって吸収剤から放出されたNOX および機関から排出
されたNOX が還元される。従って、流入排気中のH
C、COの量が十分でない場合にはNOX 吸収剤から放
出されたNOX は還元されずにそのまま下流側に流出す
ることになる。[0020] That is, HC in the inflowing exhaust gas, CO, first O 2 on the platinum Pt - immediately react with oxidized or O 2-, and then on the platinum Pt O 2 - or O 2- is consumed the HC, NO X discharged from the released NO X and the engine from the absorbent by CO is reduced even yet HC, any remaining CO is. Therefore, H in the inflow exhaust gas
C, NO X released from the NO X absorbent when the amount of CO is not sufficient will be directly flowing downstream without being reduced.
【0021】また、前述のように、NOX の放出、還元
(再生)操作を行う場合、NOX 吸収剤の雰囲気がリッ
チな条件下で再生を行うほど短時間で完全な再生が行う
ことができることが知られている。これは、NOX 吸収
剤内に硝酸イオンNO3 - の形で吸収されたNOX がN
O2 の形でNOX 吸収剤から放出される(NO3 - →N
O2 )の反応が雰囲気がリッチになる程活発になり、N
OX の放出速度が高くなるためと考えられる。Further, as described above, release of the NO X, reduction (regeneration) when performing an operation, an atmosphere of the NO X absorbent can complete regeneration is carried out in a short time as to reproduce rich conditions It is known that it can be done. This, NO X absorbent nitrate ions into the NO 3 - is absorbed in the form of the NO X is N
In the form of O 2 is released from the NO X absorbent (NO 3 - → N
The reaction of O 2 ) becomes more active as the atmosphere becomes richer,
The release rate of O X is considered to become high.
【0022】一方、NOX 吸収剤のリッチ雰囲気の度合
いが大きいと(すなわちリッチ処理を行うと)、放出さ
れたNOX の一部は、還元されてN2 になる代わりに過
剰なHC成分と反応してNH3 を生成してしまうことも
同様に知られている。従って、NOX 吸収剤の再生操作
時には還元剤の供給量は上記の未浄化NOXとアンモニ
アの発生を生じない範囲で制御する必要があり、NOX
吸収剤の再生条件が制限されることになる。本発明で
は、上記NOX 吸収剤の下流側にNOX選択還元触媒を
配置してNOX 吸収剤再生時の未浄化NOX とアンモニ
アとの両方を浄化することにより、NOX 吸収剤の再生
条件の幅を拡げて短時間で効率的な再生を行うようにし
ている。On the other hand, when the degree of the rich atmosphere of the NO X absorbent is large (that is, when the rich treatment is performed), a part of the released NO X is reduced to N 2 instead of being reduced to N 2 , and excessive HC component is removed. It is also known that NH 3 is produced by the reaction. Accordingly, the supply amount of the reducing agent at the time of regenerating operation of the NO X absorbent must be controlled within a range that does not cause the occurrence of the above unpurified NO X and ammonia, NO X
The conditions for regeneration of the absorbent will be limited. In the present invention, by purifying both the unpurified NO X and ammonia of the NO X absorbent during regeneration by placing the NO X selective reducing catalyst on the downstream side of the the NO X absorbent, regeneration of the NO X absorbent By expanding the range of conditions, efficient reproduction can be performed in a short time.
【0023】本実施例では、NOX 吸収剤5の下流側の
排気管1に配置されるNOX 選択還元触媒9としては例
えば、ゼオライトZSM−5にCu等の金属をイオン交
換して担持させたものが用いられる。NOX 選択還元触
媒9はリーン雰囲気下で適量のHCが存在するとNOX
を還元してN2 に転換することができる。更に、NO X
選択還元触媒9は、酸素の存在下でアンモニアとNOと
を反応させ、 4NH3 +4NO+O2 →4N2 +6H2 O の反応によりアンモニアをN2 に転換することが知られ
ている。すなわち、NOX 選択還元触媒9はリーン雰囲
気下でNOX とアンモニアの両方を同時に浄化すること
ができる。In this embodiment, NOXOn the downstream side of the absorbent 5
NO arranged in exhaust pipe 1XExamples of selective reduction catalyst 9
For example, a metal such as Cu is ion-exchanged with zeolite ZSM-5.
What is carried instead is used. NOXSelective touch
The medium 9 is NO when an appropriate amount of HC exists in a lean atmosphere.X
To reduce NTwoCan be converted to Furthermore, NO X
The selective reduction catalyst 9 reacts with ammonia and NO in the presence of oxygen.
And 4NHThree+ 4NO + OTwo→ 4NTwo+ 6HTwoAmmonia is converted to N by the reaction of O 2TwoIs known to convert to
ing. That is, NOXSelective reduction catalyst 9 has a lean atmosphere
NO downsideXPurifying both ammonia and ammonia at the same time
Can be.
【0024】次に、本実施例の排気浄化操作について説
明する。本実施例では、通常運転時には排気切り換え弁
2はバイパス側の排気通路3bを閉鎖する位置に保持さ
れ、排気はその全量がNOX 吸収剤5に流入する。これ
により、排気中のNOX はNOX 吸収剤5に吸収され、
NOX を除去された排気がNOX 選択還元触媒9に流入
する。このとき、NOX 選択還元触媒9は排気中に含ま
れる僅かなHCをゼオライトの細孔に吸着する。Next, the exhaust gas purifying operation of this embodiment will be described. In this embodiment, during normal operation the exhaust switching valve 2 is held in position to close the exhaust passage 3b of the bypass side, exhaust its entire amount flows into the NO X absorbent 5. Thereby, NO X in the exhaust gas is absorbed by the NO X absorbent 5,
The exhaust gas from which NO X has been removed flows into the NO X selective reduction catalyst 9. At this time, NO X selective reduction catalyst 9 adsorbs slight HC contained in the exhaust into the pores of the zeolite.
【0025】次いで、後述する所定の再生操作実行条件
が成立すると、排気切替え弁2は排気通路3a側を所定
開度まで絞り、NOX 吸収剤5に流入する排気の流量を
低減させる。これにより、NOX 吸収剤5に流入する排
気をリッチ空燃比にするために必要な還元剤の量が低減
される。また、還元剤供給装置11からはNOX 吸収剤
に流入する排気ガスの流量に対してNOX 吸収剤5の雰
囲気をかなりリッチにすることができるだけの量の還元
剤が供給される。すなわち、NOX 吸収剤5のリッチ処
理が行われる。このとき、バイパス側の排気通路3bは
全開になるため、排気の殆どは排気通路3bを流れるの
で排気抵抗は増大せず、機関の運転に影響は生じない。[0025] Then, when a predetermined regenerating operation conditions described later is satisfied, the exhaust switching valve 2 is squeezed in the exhaust passage 3a side to a predetermined opening degree, thereby reducing the flow rate of the exhaust gas flowing into the NO X absorbent 5. As a result, the amount of the reducing agent required to make the exhaust gas flowing into the NO X absorbent 5 have a rich air-fuel ratio is reduced. The reducing agent in an amount enough to be quite rich atmosphere of the NO X absorbent 5 for the flow rate of the exhaust gas flowing into the NO X absorbent is supplied from the reducing agent supply device 11. That is, the rich processing of the NO X absorbent 5 is performed. At this time, since the exhaust passage 3b on the bypass side is fully opened, most of the exhaust gas flows through the exhaust passage 3b, so that the exhaust resistance does not increase and the operation of the engine is not affected.
【0026】また、再生操作初期に流出する未浄化のN
OX と、リッチ処理により発生するアンモニア及び余剰
のHCはNOX 吸収剤5から排気通路3aに流出し、バ
イパス側の排気通路3bとの合流部で排気通路3bを流
れてきた排気ガスと混合した後NOX 選択還元触媒9に
流入する。このため、NOX 吸収剤5から流出したリッ
チ空燃比の排気ガスはバイパス側の排気通路3bを流れ
る未浄化のNOX を含む大量のリーン空燃比の排気ガス
により希釈され、NOX 選択還元触媒9に流入する排気
ガスの空燃比は全体としてリーンになる。Further, unpurified N which flows out at the beginning of the regeneration operation
O X , ammonia and excess HC generated by the rich treatment flow out of the NO X absorbent 5 into the exhaust passage 3a, and are mixed with the exhaust gas flowing through the exhaust passage 3b at a junction with the bypass-side exhaust passage 3b. After that, it flows into the NO X selective reduction catalyst 9. For this reason, the rich air-fuel ratio exhaust gas flowing out of the NO X absorbent 5 is diluted by a large amount of lean air-fuel ratio exhaust gas including unpurified NO X flowing through the bypass side exhaust passage 3b, and the NO X selective reduction catalyst The air-fuel ratio of the exhaust gas flowing into 9 becomes lean as a whole.
【0027】従ってNOX 選択還元触媒9ではリーン雰
囲気下で、流入する排気中の未浄化のNOX と、NOX
吸収剤5のリッチ処理により発生するアンモニア、HC
成分及び、NOX 吸収剤5の再生時の反応熱による排気
温度上昇のためにNOX 選択還元触媒9に吸着されてい
たHC成分が放出されたものが同時に存在することにな
り、排気中の未浄化NOX 成分とアンモニア、HCが反
応してNOX とアンモニアの両方が同時に浄化される。[0027] Accordingly lean atmosphere in the NO X selective reducing catalyst 9, and unpurified of the NO X in the exhaust gas flowing, NO X
Ammonia, HC generated by rich treatment of absorbent 5
Components and will be those HC components adsorbed on the NO X selective reducing catalyst 9 for exhaust gas temperature rise due to reaction heat during regeneration of the NO X absorbent 5 is released simultaneously exist, in the exhaust The unpurified NO X component reacts with ammonia and HC to purify both NO X and ammonia at the same time.
【0028】また、所定時間が経過してNOX 吸収剤5
の再生が完了すると切替えバルブ2はバイパス側排気通
路3bを閉鎖する位置に移動し、排気はその全量がNO
X 吸収剤5に導かれ、NOX の吸収が再開される。上述
のように、NOX 吸収剤5の下流側にNOX 選択還元触
媒9を配置して、未浄化NOX とアンモニア、HC成分
を同時に浄化することにより、NOX 吸収剤5をリッチ
処理により短時間でNOX 吸収剤を再生することが可能
になる。また、NOX 吸収剤5の再生操作時にもNOX
選択還元触媒9で排気中のNOX の浄化を行うことがで
きるため再生操作中のNOX の大気放出が防止される。Further, NO X absorbent to a predetermined time elapses 5
When the regeneration of the exhaust gas is completed, the switching valve 2 moves to the position where the bypass side exhaust passage 3b is closed, and the exhaust gas is entirely NO.
Guided to the X absorbent 5, absorption of NO X is resumed. As described above, by arranging the the NO X selective reducing catalyst 9 on the downstream side of the NO X absorbent 5, unpurified NO X and ammonia, by simultaneously purifying HC components, the rich processing of the NO X absorbent 5 a short time it is possible to reproduce the the NO X absorbent. In addition, even at the time of the regenerating operation of the NO X absorbent 5 NO X
Atmospheric release of the NO X in the regenerating operation is prevented since it is possible to purify of the NO X in the exhaust gas in the selective reduction catalyst 9.
【0029】次に、本実施例のNOX 吸収剤5の再生条
件について説明する。一般にNOX 吸収剤5とNOX 選
択還元触媒9の活性温度は相違し、通常、NOX 選択還
元触媒9はNOX 吸収剤5より高い活性温度を必要とす
る。このため、本実施例ではNOX 吸収剤5とNOX 選
択還元触媒9との両方の温度条件を考慮して、排気温度
センサ6で検出した排気温度に応じてNOX 吸収剤5の
再生条件を変更している。A description will now be given reproduction conditions of the NO X absorbent 5 in this embodiment. Generally, the activation temperatures of the NO X absorbent 5 and the NO X selective reduction catalyst 9 are different, and the NO X selective reduction catalyst 9 usually requires a higher activation temperature than the NO X absorbent 5. Therefore, in the present embodiment in consideration of both temperature and the NO X absorbent 5 and the NO X selective reducing catalyst 9, reproducing conditions of the NO X absorbent 5 in accordance with the exhaust temperature detected by the exhaust temperature sensor 6 Has changed.
【0030】図2は本実施例におけるNOX 吸収剤5の
再生操作開始条件を示すマップである。図2において縦
軸はNOX 吸収剤5がNOX 吸収に使用された時間Tを
示す。時間TはNOX 吸収剤5が吸収したNOX 量に対
応する値になる。また、図2横軸は排気温度を示し、N
OX 吸収剤5とNOX 選択還元触媒9の温度に対応す
る。ここで、温度tA はNOX 吸収剤5が活性を示す下
限温度(例えば約250度C)に対応する排気温度、温
度tB はNOX 選択還元触媒9が活性を示す下限温度
(例えば約350度C)に対応する排気温度である。本
実施例では排気温度tがtB より高い場合、すなわちN
OX 吸収剤5とNOX 選択還元触媒9の両方が活性を示
す温度領域ではNOX 吸収剤5のNOX 吸収量Tが第一
の所定値TAより大きい場合にNOX 吸収剤5の再生を
行う(図2、領域I)。FIG. 2 is a map showing conditions for starting the regeneration operation of the NO X absorbent 5 in this embodiment. The vertical axis in FIG. 2 shows the time T the NO X absorbent 5 is used in the NO X absorbent. Time T becomes a value corresponding to the amount of NO X the NO X absorbent 5 is absorbed. The horizontal axis in FIG. 2 indicates the exhaust gas temperature, and N
O X absorbent corresponding to 5 and the temperature of the NO X selective reducing catalyst 9. Here, the temperature t A is an exhaust gas temperature corresponding to the lower limit temperature (for example, about 250 ° C.) at which the NO X absorbent 5 shows the activity, and the temperature t B is the lower limit temperature (for example, about at about 250 ° C.) at which the NO X selective reduction catalyst 9 shows the activity. Exhaust temperature corresponding to 350 ° C.). In this embodiment, when the exhaust gas temperature t is higher than t B ,
O X absorbent 5 and the NO X selective NO X absorption amount T of the NO X absorbent 5 both in a temperature region showing the activity of the reduction catalyst 9 of the NO X absorbent 5 is larger than the first predetermined value T A Reproduction is performed (FIG. 2, area I).
【0031】また、排気温度tがtA とtB の間にある
場合、すなわちNOX 吸収剤5は活性温度に到達してい
るがNOX 選択還元触媒9が活性温度に到達していない
場合にはNOX 吸収剤5のNOX 吸収量Tが第二の所定
値TB (TB >TA )より大きい場合にのみNOX 吸収
剤5の再生を行い(図2、領域II)、領域Iと領域I
Iでは条件を変えてNOX 吸収剤5の再生を行ってい
る。以下、それぞれの領域における再生操作について説
明する。When the exhaust temperature t is between t A and t B , that is, when the NO X absorbent 5 has reached the activation temperature but the NO X selective reduction catalyst 9 has not reached the activation temperature. the NO X absorbent NO X absorption amount T of 5 second predetermined value T B is the (T B> T a) performs the reproduction of only the NO X absorbent 5 is greater than (2, region II), Region I and Region I
In I, the conditions are changed to regenerate the NO X absorbent 5. Hereinafter, the reproduction operation in each area will be described.
【0032】(1)領域I(t≧tB かつT≧TA の場
合) t≧tB の温度領域では、NOX 吸収剤5とNOX 選択
還元触媒9との両方が活性温度に到達しているため、N
OX 吸収剤5のNOX 吸収量がある程度大きくなった場
合(T>TA の場合)には通常の再生操作を行う。すな
わち、排気切り換え弁2を切り換えて排気通路3aを略
全閉にする所定位置に保持してNOX 吸収剤5を通過す
る排気ガス流量を絞り、還元剤供給装置11から所定量
の還元剤を供給し、NOX 吸収剤5のリッチ処理を行
う。ここでNOX 吸収量TA は、NOX 吸収剤5が飽和
するまでに充分余裕を持った吸収量である。[0032] (1) (for t ≧ t B and T ≧ T A) region I in the temperature range of t ≧ t B are both reached the activation temperature of the the NO X absorbent 5 and the NO X selective reducing catalyst 9 N
When the NO X absorption amount of the O X absorbent 5 has increased to some extent (when T> T A ), a normal regeneration operation is performed. That is, the exhaust switching valve 2 is switched to hold the exhaust passage 3 a at a predetermined position where the exhaust passage 3 a is almost fully closed, the flow rate of the exhaust gas passing through the NO X absorbent 5 is reduced, and a predetermined amount of the reducing agent is supplied from the reducing agent supply device 11. supplying, performing the rich processing of the NO X absorbent 5. Here, the NO X absorption amount T A is an absorption amount having a sufficient margin until the NO X absorbent 5 is saturated.
【0033】(2)領域II(tA ≦t<tB かつT≧
TB の場合) tA ≦t<tB の温度領域ではNOX 選択還元触媒9は
活性温度に到達していないので、通常はNOX 吸収剤5
の再生を行わずできるだけ領域Iの条件が成立するのを
待つようにし、NOX 吸収剤5のNOX 吸収量が増大し
てNOX 吸収剤5が飽和する恐れがある値になった場合
(T≧TB の場合)にのみNOX 吸収剤5の再生を行
う。(2) Region II (t A ≦ t <t B and T ≧
Since T For B) t A ≦ t <NO X selective reduction catalyst 9 is in the temperature range of t B does not reach the activation temperature, usually the NO X absorbent 5
If the condition of possible areas I without play so as to wait for the establishment, NO X absorption of the NO X absorbent 5 is the NO X absorbent 5 increases becomes a value that may be saturated ( for reproducing of the NO X absorbent 5 only if T ≧ T B).
【0034】また、再生操作を実行する場合にはできる
だけNOX 選択還元触媒9の温度を速く上昇させて領域
Iに移行できるように、排気温度tを上昇させる操作を
行う。すなわち、領域IIでは再生操作実行時に領域I
の場合よりもNOX 吸収剤5を通過する排気ガス流量が
増大する位置に排気切り換え弁2を保持する。また、還
元剤供給装置11から供給する還元剤の供給量も排気ガ
ス流量に応じて増大させてNOX 吸収剤5上での還元剤
の酸化反応を活発にする。これによりNOX 選択還元触
媒9に流入する排気ガス温度が上昇し、NOX 選択還元
触媒9の温度が上昇するためNOX 選択還元触媒9が速
やかに活性温度に到達する。Further, as it can be migrated to the region I and as fast as possible to raise the temperature of the NO X selective reducing catalyst 9 in the case of executing the reproduction operation, performs an operation to raise the exhaust gas temperature t. That is, in the area II, when the reproduction operation is performed, the area I
Exhaust gas flow through the the NO X absorbent 5 holds the exhaust switching valve 2 to a position to increase than for. In addition, the supply amount of the reducing agent supplied from the reducing agent supply device 11 is also increased in accordance with the flow rate of the exhaust gas to activate the oxidation reaction of the reducing agent on the NO X absorbent 5. As a result, the temperature of the exhaust gas flowing into the NO X selective reduction catalyst 9 increases, and the temperature of the NO X selective reduction catalyst 9 increases, so that the NO X selective reduction catalyst 9 quickly reaches the activation temperature.
【0035】なお、還元剤供給量は排気酸素濃度センサ
7の出力に応じて、NOX 吸収剤5を通過する排気ガス
の空燃比が理論空燃比付近になるようにフィードバック
制御してもよい。また、NOX 選択還元触媒9に予め電
気ヒータを設けておき、領域IIで再生を行なう場合に
通電してNOX 選択還元触媒9を加熱するようにすれば
NOX 選択還元触媒9を更に速く昇温させることができ
る。[0035] Incidentally, the reducing agent supply amount according to an output of the exhaust oxygen concentration sensor 7, the air-fuel ratio of the exhaust gas passing through the the NO X absorbent 5 may be feedback controlled so that the vicinity of the stoichiometric air-fuel ratio. Further, NO in the X selective reducing catalyst 9 provided in advance an electric heater, further faster the NO X selective reducing catalyst 9 if to heat the NO X selective reducing catalyst 9 is energized when reproducing in the region II The temperature can be raised.
【0036】また、NOX 選択還元触媒9が活性温度に
到達した後は排気切り換え弁2と還元剤供給装置11は
領域Iの場合と同様に制御され、NOX 吸収剤5の通常
の再生操作が行われる。図3に上記再生条件の判定フロ
ーチャートを示す。本ルーチンはECU20により所定
時間毎に実行され、判定された領域に応じて再生操作実
行フラグFと還元剤供給制御フラグKの値が設定され
る。Further, NO X after selective reduction catalyst 9 reaches the activation temperature and the exhaust switching valve 2 reducing agent supply device 11 is controlled as in the region I, normal playback operation of the NO X absorbent 5 Is performed. FIG. 3 shows a flowchart for determining the reproduction condition. This routine is executed by the ECU 20 at predetermined time intervals, and the values of the regeneration operation execution flag F and the reducing agent supply control flag K are set according to the determined area.
【0037】図3においてステップ301から303は
上記領域の判定動作を示す。また、ステップ304、3
05はステップ301から303で条件が上記領域Iに
あると判定された場合であり、ステップ304では再生
操作実行フラグFの値が“1”にセットされ、ステップ
305で還元剤供給量フラグKの値が“1”にセットさ
れる。In FIG. 3, steps 301 to 303 show the above-mentioned area determination operation. Steps 304 and 3
05 is a case where it is determined in Steps 301 to 303 that the condition is in the region I. In Step 304, the value of the regeneration operation execution flag F is set to “1”, and in Step 305, the value of the reducing agent supply amount flag K is set. The value is set to "1".
【0038】フラグFの値が“1”にセットされるとE
CU20により別途実行される図示しないルーチンによ
り排気切り換え弁2は排気通路3aを略全閉にする第一
の所定開度に保持される。同様に、フラグKが“1”に
セットされるとECU20により別途行われる図示しな
いルーチンにより還元剤供給装置11からの還元剤供給
量は排気切り換え弁2の開度に対応してNOX 吸収剤5
をリッチ処理するのに必要な量に制御される。When the value of the flag F is set to "1", E
The exhaust switching valve 2 is maintained at a first predetermined degree of opening that almost completely closes the exhaust passage 3a by a routine (not shown) separately executed by the CU 20. Similarly, the flag K is "1" reducing agent supply amount from the reducing agent supply device 11 by a routine not shown separately performed by the is set ECU20 The corresponding to the opening degree of the exhaust switching valve 2 NO X absorbent 5
Is controlled to an amount necessary to perform the rich processing.
【0039】ステップ306、307はステップ301
から303で条件が上記領域IIにあると判定された場
合であり、フラグFとフラグKの値はそれぞれ“2”に
セットされる。これにより、排気制御弁2の開度は前記
第一の開度より大きい第二の所定開度に保持され、NO
X 吸収剤5を通過する排気ガス流量は領域Iより大きい
値に設定される。また、還元剤供給装置11からの還元
剤供給量は、排気切換え弁2の開度に対応してNOX 吸
収剤5をリッチ処理するのに必要な量に制御される。Steps 306 and 307 correspond to step 301
To 303, when the condition is determined to be in the area II, the values of the flag F and the flag K are respectively set to “2”. As a result, the opening of the exhaust control valve 2 is maintained at the second predetermined opening which is larger than the first opening, and NO
The flow rate of the exhaust gas passing through the X absorbent 5 is set to a value larger than the region I. Further, the amount of the reducing agent supplied from the reducing agent supply device 11 is controlled to an amount necessary for performing the rich treatment of the NO X absorbent 5 in accordance with the opening degree of the exhaust gas switching valve 2.
【0040】ステップ306、307はステップ301
から303で条件が上記領域I、領域II以外の領域に
あると判定された場合であり、フラグFとフラグKの値
はそれぞれゼロリセットされる。この場合にはNOX 吸
収剤5の再生操作は行われず、排気切り換え弁2はバイ
パス側排気通路3bを全閉にして排気の全量をNOX吸
収剤5に導くとともに、還元剤供給装置11からの還元
剤供給は停止される。Steps 306 and 307 correspond to step 301
To 303, when the condition is determined to be in an area other than the areas I and II, the values of the flag F and the flag K are reset to zero. In this case, the regeneration operation of the NO X absorbent 5 is not performed, and the exhaust switching valve 2 fully closes the bypass side exhaust passage 3 b to guide the entire amount of exhaust gas to the NO X absorbent 5. Is stopped.
【0041】次に、図4を用いて本発明の別の実施例を
説明する。本実施例では、バイパス側排気通路3bに二
次空気を供給する二次空気供給装置15が設けられてい
る点と、NOX 選択還元触媒9入口排気温度を検出する
排気温度センサ16とが新たに設けられている点が図1
の構成と相違する。前述のように、NOX 選択還元触媒
9の活性温度は一般にNOX 吸収剤5の活性温度よりも
高いため、NOX 吸収剤5の再生操作はできるだけ高い
排気温度領域で行うことが好ましい。ところが、NOX
吸収剤5とNOX 選択還元触媒9にはそれぞれ使用上限
温度があり、排気温度がこの上限温度を越えると劣化が
加速される。また、一般にNOX 選択還元触媒9の使用
上限温度はNOX 吸収剤5の使用上弦温度より高いた
め、NOX 吸収剤5再生時の排気温度の上限はNOX 選
択還元触媒9の使用上限温度で規制されてしまう。Next, another embodiment of the present invention will be described with reference to FIG. In this embodiment, new and that the secondary air supply system 15 for supplying secondary air to the bypass-side exhaust passage 3b is provided, and the exhaust temperature sensor 16 for detecting the the NO X selective reducing catalyst 9 inlet exhaust temperature Fig. 1
Configuration. As described above, the activation temperature of the NO X selective reducing catalyst 9 is generally higher than the activation temperature of the NO X absorbent 5, the regenerating operation of the NO X absorbent 5 is preferably carried out at as high as possible exhaust gas temperature region. However, NO X
Each of the absorbent 5 and the NO X selective reducing catalyst 9 is the use upper limit temperature, exhaust temperature and deterioration is accelerated beyond the upper limit temperature. Further, since the upper limit temperature of use of the NO X selective reduction catalyst 9 is generally higher than the first use temperature of the NO X absorbent 5, the upper limit of the exhaust temperature at the time of regeneration of the NO X absorbent 5 is the upper limit temperature of the use of the NO X selective reduction catalyst 9. It is regulated by.
【0042】本実施例では、NOX 選択還元触媒9に二
次空気を供給して流入排気温度を低下させることによ
り、NOX 吸収剤5再生時の排気温度の上限を拡大して
いる。図4において、二次空気供給装置15はエアポン
プ等の適宜な加圧空気源15aと流量制御弁15bとを
そなえ、ECU20からの制御信号により、エアポンプ
15aの発停と流量制御弁15bの開度を制御すること
により所定条件下でバイパス側排気通路3bに二次空気
が供給される。[0042] In this embodiment, by lowering the supply to inflowing exhaust gas temperature of the secondary air to the NO X selective reducing catalyst 9 has expanded the upper limit of the exhaust temperature during the NO X absorbent 5 play. In FIG. 4, the secondary air supply device 15 includes an appropriate pressurized air source 15a such as an air pump and a flow control valve 15b, and starts and stops the air pump 15a and opens the flow control valve 15b according to a control signal from the ECU 20. Is controlled, the secondary air is supplied to the bypass-side exhaust passage 3b under predetermined conditions.
【0043】図5は、本実施例における再生操作開始条
件と二次空気導入条件とを示す図2と同様なマップであ
る。図5においてtA 、tB 、TA 、TB 及び領域I、
IIは図2と同様な値を示す。また、tC はNOX 選択
還元触媒9の使用上限温度に対して余裕をみた低い温度
とされ、本実施例では例えば600度C程度に設定され
る。FIG. 5 is a map similar to FIG. 2 showing the regeneration operation start condition and the secondary air introduction condition in this embodiment. In FIG. 5, t A , t B , T A , T B and region I,
II shows the same value as FIG. In addition, t C is set to a temperature lower than the upper limit temperature of use of the NO X selective reduction catalyst 9 with a margin, and is set to, for example, about 600 ° C. in the present embodiment.
【0044】本実施例では、NOX 吸収剤5の再生操作
は二次空気の供給制御とは独立して図5のマップに従っ
て制御される。本実施例のNOX 吸収剤5の再生操作及
び領域I、領域IIの設定は図2、図3と同様であるの
でここでは説明を省略する。また、図5領域IIIは二
次空気の導入が行われる領域を示す。本実施例ではNO
X 吸収剤5出口の排気温度センサ6により検出した排気
温度がNOX 選択還元触媒9の使用上限温度tC を越え
た場合には、NOX 吸収剤5の再生操作の有無にかかわ
らず(すなわち、領域Iにあるか否かにかかわらず)二
次空気の導入が行われる。また、二次空気の供給量はN
OX 選択還元触媒9入口排気温度センサ16の出力に基
づいて、NOX 選択還元触媒9入口温度がtC以下にな
るようにECU20によりフィードバック制御される。
これにより、排気温度が高い状態でNOX 吸収剤5の再
生操作が実行された場合に、再生操作によりNOX 吸収
剤5出口排気温度が上昇した場合でもNOX 選択還元触
媒9は使用上限温度以下の温度に保たれるため、劣化が
加速されることがない。[0044] In this embodiment, the regenerating operation of the NO X absorbent 5 is controlled in accordance with the map of FIG. 5 independently of the supply control of secondary air. The NO X absorbent 5 playback operation and the area I of the present embodiment, the region II setting will be omitted here because FIG 2 is similar to FIG. 3. FIG. 5 shows a region III in which the secondary air is introduced. In this embodiment, NO
When the exhaust gas temperature detected by the exhaust gas temperature sensor 6 at the outlet of the X absorbent 5 exceeds the use upper limit temperature t C of the NO X selective reduction catalyst 9, regardless of the presence or absence of the regeneration operation of the NO X absorbent 5 (ie, , Whether in region I or not). The supply amount of the secondary air is N
Based on the output of the O X selective reduction catalyst 9 inlet exhaust temperature sensor 16, NO X selective reduction catalyst 9 inlet temperature is feedback controlled by the ECU20 to be less than t C.
Thus, when the reproduction operation of the NO X absorbent 5 at the exhaust gas temperature is high is performed, NO X selective reduction catalyst 9 even when the NO X absorbent 5 outlet exhaust temperature is increased by reproducing operations using upper limit temperature Since the temperature is kept below, deterioration is not accelerated.
【0045】[0045]
【発明の効果】本発明の排気浄化装置は、NOX 吸収剤
の下流側にリーン排気条件下で排気中のNOX とHCと
を選択的に反応させNOX を分解するNOX 選択還元触
媒を配置すると共に、NO X 吸収剤再生操作時にNO X
選択還元触媒に流入する排気の空燃比をリーンに維持す
るようにしたことにより、NO X 吸収剤再生操作初期に
発生する未浄化NO X と再生操作中にNO X 吸収剤で発
生するアンモニアとの両方をNO X 選択還元触媒により
浄化することが可能となる。このため、本発明によれ
ば、NO X 吸収剤の再生条件の範囲を拡げ、短時間で効
率的な再生を行うことが可能となる。 Exhaust purification apparatus of the present invention exhibits, NO X absorbent downstream the NO X and HC and the selectively degrades the NO X by reacting the NO X selective reducing catalyst in the exhaust in lean exhaust conditions with placing, NO X when the NO X absorbent regenerating operation
Maintain lean air-fuel ratio of exhaust gas flowing into the selective reduction catalyst
By you so that, in the NO X absorbent regenerating operation Initial
Generated unpurified NO X and NO X absorbent during regeneration operation
By the NO X selective reducing catalyst both with ammonia to raw
It becomes possible to purify. Therefore, according to the present invention,
If, expanding the range of playing conditions of the NO X absorbent, effect in a short period of time
It is possible to perform efficient reproduction.
【図1】本発明の実施例を説明する図である。FIG. 1 is a diagram illustrating an embodiment of the present invention.
【図2】図1の実施例の再生操作開始条件を示す図であ
る。FIG. 2 is a diagram showing a reproduction operation start condition in the embodiment of FIG. 1;
【図3】図1の実施例の再生条件の判定を示すフローチ
ャートである。FIG. 3 is a flowchart showing a determination of a reproduction condition in the embodiment of FIG. 1;
【図4】本発明の図1とは別の実施例を説明する図であ
る。FIG. 4 is a view for explaining another embodiment of the present invention different from FIG. 1;
【図5】図4の実施例の再生操作開始条件を示す図2と
同様な図である。FIG. 5 is a view similar to FIG. 2, showing a reproduction operation start condition of the embodiment of FIG. 4;
【図6】本発明のNOX 吸収剤の吸放出作用を説明する
図である。FIG. 6 is a diagram illustrating the absorption and release action of the NO X absorbent of the present invention.
1…排気管 2…排気切り換え弁 3a、3b…分岐排気通路 5…NOX 吸収剤 6…排気温度センサ 7…排気酸素濃度センサ 9…NOX 選択還元触媒 11…還元剤供給装置 15…二次空気供給装置 20…エンジン制御回路(ECU)1 ... exhaust pipe 2 ... exhaust switching valve 3a, 3b ... branch exhaust passage 5 ... NO X absorbent 6 ... exhaust gas temperature sensor 7 ... exhaust oxygen concentration sensor 9 ... NO X selective reducing catalyst 11 ... reducing agent supply device 15 ... secondary Air supply device 20 ... Engine control circuit (ECU)
───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 昭62−106826(JP,A) 実開 平4−117136(JP,U) (58)調査した分野(Int.Cl.6,DB名) F01N 3/24 F01N 3/08 F01N 3/18 F01N 3/20 F01N 3/28 301──────────────────────────────────────────────────続 き Continuation of the front page (56) References JP-A-62-106826 (JP, A) JP-A-4-117136 (JP, U) (58) Fields investigated (Int. Cl. 6 , DB name) F01N 3/24 F01N 3/08 F01N 3/18 F01N 3/20 F01N 3/28 301
Claims (1)
内燃機関の排気通路に、流入排気の空燃比がリーンのと
きにNOX を吸収し流入排気の酸素濃度が低下したとき
に吸収したNOX を放出するNOX 吸収剤を配置して排
気中のNOXを吸収させ、その後NOX 吸収剤に流入す
る排気空燃比をリッチにして吸収したNOX をNOX 吸
収剤から放出させると共に該NOX を還元浄化する内燃
機関の排気浄化装置において、前記NOX 吸収剤の下流
側にリーン排気空燃比条件下で排気中のNOX を還元剤
と選択的に反応させ得るNOX 選択還元触媒と、前記N
O X 吸収剤に流入する排気空燃比をリッチにして吸収し
たNO X を放出させるときに前記NO X 選択還元触媒に
流入する排気の空燃比をリーンに維持する手段とを設け
たことを特徴とする内燃機関の排気浄化装置。In an exhaust passage of claim 1 an internal combustion engine capable of performing combustion of the lean air-fuel ratio, the air-fuel ratio of the inflowing exhaust gas is the oxygen concentration of the inflowing exhaust absorbs NO X when the lean absorbed when reduced NO by placing the NO X absorbent to release the X to absorb NO X in the exhaust gas, the causes subsequent the NO X absorbent NO X which the exhaust air-fuel ratio flowing absorbed in the rich released from the NO X absorbent in the exhaust purification system of an internal combustion engine to reduce and purify NO X, the NO X in the downstream side of the absorber NO X in the exhaust gas in the lean exhaust air-fuel ratio conditions may selectively reacting with a reducing agent the NO X selective reducing catalyst And the N
The exhaust air-fuel ratio flowing into the O X absorbent in the rich absorbing
The NO X in the the NO X selective reducing catalyst when to release the
Means for maintaining the air-fuel ratio of the inflowing exhaust gas lean .
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5741293A JP2845080B2 (en) | 1993-03-17 | 1993-03-17 | Exhaust gas purification device for internal combustion engine |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5741293A JP2845080B2 (en) | 1993-03-17 | 1993-03-17 | Exhaust gas purification device for internal combustion engine |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH06272545A JPH06272545A (en) | 1994-09-27 |
| JP2845080B2 true JP2845080B2 (en) | 1999-01-13 |
Family
ID=13054938
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5741293A Expired - Lifetime JP2845080B2 (en) | 1993-03-17 | 1993-03-17 | Exhaust gas purification device for internal combustion engine |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2845080B2 (en) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2724377B1 (en) * | 1994-09-09 | 1996-10-31 | Saint Gobain Vitrage | EMAIL COMPOSITION FOR GLASS SUBSTRATE |
| JP3427581B2 (en) * | 1994-09-13 | 2003-07-22 | トヨタ自動車株式会社 | Exhaust gas purification device for internal combustion engine |
| US6119452A (en) * | 1995-11-17 | 2000-09-19 | Toyota Jidosha Kabushiki Kaisha | Device for purifying exhaust gas of internal combustion engine |
| DE19740702C1 (en) * | 1997-09-16 | 1998-11-19 | Siemens Ag | Exhaust purification system management for e.g. lean-running diesel engine |
| JP3518398B2 (en) * | 1999-03-11 | 2004-04-12 | トヨタ自動車株式会社 | Exhaust gas purification device for internal combustion engine |
| DE10021071C1 (en) * | 2000-04-29 | 2002-03-07 | Omg Ag & Co Kg | Process for removing nitrogen oxides from a flue gas stream containing oxygen |
| DE10300298A1 (en) | 2003-01-02 | 2004-07-15 | Daimlerchrysler Ag | Exhaust gas aftertreatment device and method |
| US7213395B2 (en) * | 2004-07-14 | 2007-05-08 | Eaton Corporation | Hybrid catalyst system for exhaust emissions reduction |
| JP2009221873A (en) * | 2008-03-13 | 2009-10-01 | Toyota Motor Corp | Exhaust emission control system for internal combustion engine |
| US20140356237A1 (en) * | 2012-02-07 | 2014-12-04 | Toyota Jidosha Kabushiki Kaisha | Exhaust gas purification apparatus for internal combustion engine |
| JP2019190417A (en) * | 2018-04-27 | 2019-10-31 | いすゞ自動車株式会社 | Exhaust emission control device and vehicle |
-
1993
- 1993-03-17 JP JP5741293A patent/JP2845080B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH06272545A (en) | 1994-09-27 |
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