JPH0616813B2 - Ventilation gas purification method in road tunnel - Google Patents
Ventilation gas purification method in road tunnelInfo
- Publication number
- JPH0616813B2 JPH0616813B2 JP62313777A JP31377787A JPH0616813B2 JP H0616813 B2 JPH0616813 B2 JP H0616813B2 JP 62313777 A JP62313777 A JP 62313777A JP 31377787 A JP31377787 A JP 31377787A JP H0616813 B2 JPH0616813 B2 JP H0616813B2
- Authority
- JP
- Japan
- Prior art keywords
- adsorbent
- nox
- gas
- ventilation gas
- ventilation
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
Classifications
-
- E—FIXED CONSTRUCTIONS
- E21—EARTH OR ROCK DRILLING; MINING
- E21F—SAFETY DEVICES, TRANSPORT, FILLING-UP, RESCUE, VENTILATION, OR DRAINING IN OR OF MINES OR TUNNELS
- E21F1/00—Ventilation of mines or tunnels; Distribution of ventilating currents
- E21F1/003—Ventilation of traffic tunnels
Landscapes
- Engineering & Computer Science (AREA)
- Mining & Mineral Resources (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Geology (AREA)
- Treating Waste Gases (AREA)
Description
【発明の詳細な説明】 産業上の利用分野 この発明は、道路用の山岳トンネル、地下道路、シェル
ター付き道路等(この明細書において、これらを総称し
て「道路トンネル」という)において、内部の汚染空気
を換気し、換気ガスを窒素酸化物(NOx)除去等の浄
化処理に付す換気ガスの浄化方法に関する。TECHNICAL FIELD The present invention relates to a mountain tunnel for roads, an underground road, a road with a shelter, etc. (in this specification, these are collectively referred to as “road tunnel”) The present invention relates to a method for purifying ventilation gas, in which contaminated air is ventilated and the ventilation gas is subjected to purification treatment such as nitrogen oxide (NOx) removal.
発明の背景 長距離でかつ自動車と交通量の多い道路トンネルでは、
ドライバーや歩行者等の健康を保護し、かつトンネル内
の煤煙の透過率を改善するために、内部の汚染空気を換
気する必要がある。また比較的短距離の道路トンネルに
おいても、都市部あるいはその近郊にあるものについて
は、出入口部に集中した一酸化炭素ガスやNOx等によ
る大気汚染に対処する目的で、トンネル内の汚染空気を
換気する必要がある。BACKGROUND OF THE INVENTION In a long-distance road tunnel with a lot of cars and traffic,
It is necessary to ventilate the contaminated air inside in order to protect the health of drivers and pedestrians and improve the permeability of soot in the tunnel. In addition, even in a relatively short distance road tunnel, for the one in the urban area or its suburbs, the contaminated air in the tunnel is ventilated in order to cope with the air pollution due to carbon monoxide gas and NOx concentrated in the entrance and exit. There is a need to.
しかしながら、換気ガスをそのままトンネルの周辺に放
散するのでは、地域的な環境改善に反するばかりか、特
に自動車排ガスによる汚染が平面的に拡大しつつある都
市部あるいはその近郊においては、汚染度の高い汚染地
域をさらに拡大させることにもなりかねない。既設道路
の公害対策として道路をトンネル化したり、シェルター
を設置する場合も、前述の事情は全く同じである。However, if ventilation gas is diffused around the tunnel as it is, it is not only against the improvement of the local environment, but also the pollution level is high especially in the urban area where the exhaust gas pollution is spreading in the plane or its suburbs. It could lead to further expansion of the contaminated area. The above-mentioned situation is exactly the same even when a road is tunneled or a shelter is installed as a measure against pollution of an existing road.
したがって、道路トンネルから出た換気ガスを効率よく
NOx除去処理することができる方法が、要望せられて
いる。Therefore, there is a demand for a method capable of efficiently removing NOx from ventilation gas emitted from a road tunnel.
従来の技術 固定発生原からのNOxの除去法は、従来から主として
各種ボイラ燃焼排ガスの浄化ろ目的として検討されてお
り、大別すると、(1) 接触還元法、(2) 乾式吸着法、
(3) 湿式吸収法がある。そして、従来と研究は上述の如
くボイラ排ガスを対象としているため、処理すべき排ガ
スの温度は200℃以上であるか、または付近にガス加
熱用熱源があることを想定して研究が行なわれ、また除
去すべき排ガスのNOx濃度は100ppm 以上であると
して検討がなされている。2. Description of the Related Art Conventional methods for removing NOx from fixed sources have been mainly studied for the purpose of purification of various boiler combustion exhaust gases, and roughly classified into (1) catalytic reduction method, (2) dry adsorption method,
(3) There is a wet absorption method. Since the conventional and research target boiler exhaust gas as described above, research is conducted assuming that the temperature of the exhaust gas to be treated is 200 ° C. or higher, or that there is a heat source for gas heating in the vicinity. Further, it is considered that the NOx concentration of the exhaust gas to be removed is 100 ppm or more.
発明の解決しようとする問題点 ところで、道路トンネルの概略的な特性を想定すれば、
処理すべきガスのNOx濃度は5ppm 以下の低濃度であ
り、また温度はほぼ常温である。そしてガス中には一酸
化炭素ガス、各種ハイドロカーボン蒸気、オイルミス
ト、ジーゼル煤煙等の大気汚染物質が含まれている。ま
た換気量はトンネル内の交通量に応じてコントロールさ
れるので、一日に30〜100%程度の大きな幅で変動
すると考えられる。Problems to be Solved by the Invention By the way, assuming the general characteristics of a road tunnel,
The NOx concentration of the gas to be treated is a low concentration of 5 ppm or less, and the temperature is almost room temperature. The gas contains carbon monoxide gas, various hydrocarbon vapors, oil mist, diesel soot and other air pollutants. Further, since the ventilation volume is controlled according to the traffic volume in the tunnel, it is considered that it fluctuates in a large range of about 30 to 100% per day.
以上の点を考慮に入れると、道路トンネルにおける換気
ガスの浄化にはつぎの事項が要求せられる。Taking the above points into consideration, the following items are required to purify ventilation gas in road tunnels.
(1) 換気ガス中の5pp 以下の低濃度のNOxを、換
気ガスを昇温することなく、高い効率で除去できるこ
と、 (2) 浄化設備の運転時のエネルギー消費を極力低減
し、特に設備周辺への熱公害を起こさないこと、 (3) 浄化設備は市街地に設置されても周辺の建造物と
調和する規模および形態であること、望ましくは設備全
体に屋内に収納できること、 (4) 浄化操作に伴って廃液や固体廃棄物を生じないこ
と。(1) It is possible to remove NOx with a low concentration of 5 pp or less in the ventilation gas with high efficiency without raising the temperature of the ventilation gas. (2) Energy consumption during operation of the purification equipment is reduced as much as possible, especially around the equipment. (3) Even if installed in an urban area, the purification equipment must be of a scale and form that is in harmony with the surrounding buildings, and it is desirable that the entire equipment can be stored indoors. (4) Purification operation Do not generate waste liquid or solid waste with
これに対し、従来技術では、上述の如く、対象とする排
ガスの温度は200℃以上の高温であり、また排ガスの
NOx濃度は100ppm 以上の高濃度であるので、この
従来技術をそのまま道路トンネルの換気ガスの浄化に適
用することはできない。On the other hand, in the conventional technique, as described above, the temperature of the target exhaust gas is a high temperature of 200 ° C. or higher, and the NOx concentration of the exhaust gas is a high concentration of 100 ppm or higher. It cannot be applied to the purification of ventilation gases.
この発明は、上記の如き実情に鑑み、道路トンネルから
出た換気ガスを効率よくNOx除去処理することができ
る実用的な換気ガス浄化方法を提供することを目的とす
る。In view of the above situation, an object of the present invention is to provide a practical ventilation gas purification method that can efficiently perform NOx removal processing on ventilation gas emitted from a road tunnel.
問題点を解決するための手段 この発明による換気ガスの浄化方法は、道路トンネルか
ら出たNOx濃度5ppm以下の換気ガスを、銅および
/またはバナジウムを含むゼオライト系吸着剤で乾式処
理して、主としてNOxを吸着除去し、NOx吸着状態
の吸着剤をNH3 を含む高温空気で処理して再生させる
ことを特徴とする。Means for Solving the Problems In the method for purifying ventilation gas according to the present invention, a ventilation gas having a NOx concentration of 5 ppm or less discharged from a road tunnel is dry-treated with a zeolite adsorbent containing copper and / or vanadium, and is mainly used. It is characterized in that NOx is adsorbed and removed, and the adsorbent in the NOx adsorbed state is treated with hot air containing NH 3 to be regenerated.
この発明の好ましい実施態様においては、吸着剤とし
て、銅、バナジウム等の金属酸化物を含むゼオライト系
吸着剤を用いる。In a preferred embodiment of the present invention, a zeolitic adsorbent containing a metal oxide such as copper or vanadium is used as the adsorbent.
再生工程において、NOxは還元剤としてのNH3 によ
って窒素ガスに選択的に還元されて吸着剤から脱着す
る。その結果、吸着剤が再生せられる。吸着剤の再生は
温度100℃以上、好ましくは150℃以上で行なわれ
る。In the regeneration step, NOx is selectively reduced to nitrogen gas by NH 3 as a reducing agent and desorbed from the adsorbent. As a result, the adsorbent is regenerated. Regeneration of the adsorbent is carried out at a temperature of 100 ° C or higher, preferably 150 ° C or higher.
吸着および再生は、好ましくは移動床式の吸着部、予熱
・冷却部および再生部によって実施される。ただし、吸
着剤を固定床に充填し、浄化すべき換気ガスと再生用の
NH3 含有高温空気とを吸着剤固定床に交番的に流通さ
せる方法をとってもよい。Adsorption and regeneration are preferably carried out by a moving bed type adsorption section, preheating / cooling section and regeneration section. However, a method may be used in which the fixed bed is filled with the adsorbent and the ventilation gas to be purified and the NH 3 -containing high temperature air for regeneration are alternately passed through the fixed bed.
この発明の基本プロセスを第1図に基づいて説明する。The basic process of the present invention will be described with reference to FIG.
道路トンネル(1) から換気ブロワー(2) によって排出さ
れた換気ガスは、吸着塔(3) に導かれ、吸着塔(3) に充
填された吸着剤によって乾式処理され、処理ガスは系外
へ放出される。吸着剤としては、銅、バナジウム等の金
属酸化物を含むゼオライト系吸着剤が用いられる。The ventilation gas discharged from the road tunnel (1) by the ventilation blower (2) is guided to the adsorption tower (3) and is dry-processed by the adsorbent filled in the adsorption tower (3), and the processed gas is discharged outside the system. Is released. As the adsorbent, a zeolite adsorbent containing a metal oxide such as copper or vanadium is used.
NOxを吸着した吸着剤は、吸着塔(3) から連続的ない
し断続的に排出されて再生塔(4) に送られる。再生塔
(4) では吸着剤はNH3 を含む高温空気で接触処理され
る。この空気は循環ブロワー(5) で再生塔(4) に送ら
れ、かつヒーター(6) で100℃以上に加熱される。N
H3 はボンベ(7) から加熱空気に添加される。その結
果、NOxは還元剤としてのNH3 によって窒素ガスに
還元されて吸着剤から脱着し、吸着剤が再生せられる。
再生した吸着剤は再生塔(4) から連続的ないし断続的に
排出され、再び吸着塔(3) に供給される。The adsorbent that has adsorbed NOx is continuously or intermittently discharged from the adsorption tower (3) and sent to the regeneration tower (4). Regeneration tower
In (4), the adsorbent is contact-treated with hot air containing NH 3 . This air is sent to the regeneration tower (4) by the circulation blower (5) and heated to 100 ° C. or higher by the heater (6). N
H 3 is added to the heated air from the cylinder (7). As a result, NOx is reduced to nitrogen gas by NH 3 as a reducing agent, desorbed from the adsorbent, and the adsorbent is regenerated.
The regenerated adsorbent is continuously or intermittently discharged from the regeneration tower (4) and supplied to the adsorption tower (3) again.
実施例 つぎに、この発明の実施例について具体的に説明する。EXAMPLES Next, examples of the present invention will be specifically described.
操作プロセス 下記表1に示す交通条件の道路トンネルにおいて、この
発明による浄化方法を適用する。表1の条件から算出す
ると、トンネル内の煤煙透過率を40%以上に保つため
には換気量はトンネル1km当り150万Nm3/h必要で
ある。この場合の換気ガスの特性は表2に示すとおりで
ある。換気ガスの浄化設備をトンネル333m当り1基
設けるとすると、浄化設備の処理容量は50万Nm3/h
となる。Operation Process The purification method according to the present invention is applied to a road tunnel under the traffic conditions shown in Table 1 below. Calculated from the conditions in Table 1, the ventilation volume is required to be 1.5 million Nm 3 / h per 1 km of the tunnel in order to keep the soot permeability in the tunnel at 40% or more. The characteristics of the ventilation gas in this case are as shown in Table 2. Assuming that one ventilation gas purification facility is installed for every 333 m of tunnel, the treatment capacity of the purification facility is 500,000 Nm 3 / h.
Becomes
つぎに、換気ガスの浄化設備について説明する。 Next, a ventilation gas purification facility will be described.
第2図および第3図において、道路トンネル(11)から換
気ブロワー(12)によって排出された換気ガスは、浄化設
置の吸着部(13)に導かれる。浄化設備は、換気ガス中の
NOxを吸着剤で吸着するNOx吸着部(13)と、NOx
吸着状態の未再生吸着剤を予熱し、かつ再生後の吸着剤
を冷却する予熱・冷却部(18)と、予熱・冷却部(18)から
来た吸着剤をNOx脱着処理する吸着剤再生部(14)とよ
り主として構成されている。NOx吸着部(13)、予熱・
冷却部(18)および吸着剤再生部(14)はいずれも移動床式
であって、NOx吸着剤を保持した複数の移動ブロック
(19)がNOx吸着剤(13)および予熱・冷却部(18)の内部
に一列に並べられている。移動ブロック(19)はNOx吸
着部(13)内を換気ガス流れに対して向流方向に断続的に
移動させられ、NOx吸着部(13)の終端に達したものは
通路(20)を経て予熱・冷却部(18)へ送られ、この内部を
やはり断続的に始端から終端に向けて移動させられる。
ついで移動ブロック(19)は予熱・冷却部(18)の中間部に
おいて抜き出されて、通路(21)を経て吸着剤再生部(14)
へ送られ、吸着剤再生後の移動ブロック(19)は再び通路
(21)を経て予熱・冷却部(18)のブロック列の元の位置に
挿入される。ついで移動ブロック(19)は予熱・冷却部(1
8)の終端から通路(22)を経てNOx吸着部(13)の始端に
戻される。In FIGS. 2 and 3, the ventilation gas discharged from the road tunnel (11) by the ventilation blower (12) is guided to the adsorption section (13) of the purification installation. The purification equipment consists of a NOx adsorber (13) that adsorbs NOx in the ventilation gas with an adsorbent and a NOx adsorbent.
A preheating / cooling unit (18) that preheats the unregenerated adsorbent in an adsorbed state and cools the adsorbent after regeneration, and an adsorbent regeneration unit that NOx desorbs the adsorbent that came from the preheating / cooling unit (18). It is mainly composed of (14). NOx adsorption part (13), preheating
Both the cooling unit (18) and the adsorbent regeneration unit (14) are of a moving bed type, and have a plurality of moving blocks holding NOx adsorbent.
(19) are arranged in a line inside the NOx adsorbent (13) and the preheating / cooling section (18). The moving block (19) is intermittently moved in the NOx adsorbing part (13) in a countercurrent direction to the ventilation gas flow, and the one reaching the end of the NOx adsorbing part (13) passes through the passage (20). It is sent to the preheating / cooling section (18), and the inside of this is also intermittently moved from the start end to the end.
Then, the moving block (19) is withdrawn in the middle of the preheating / cooling section (18), and passes through the passage (21) to regenerate the adsorbent (14).
Sent to the moving block (19) after regeneration of the adsorbent.
It is inserted into the original position of the block row of the preheating / cooling section (18) via (21). The moving block (19) is then connected to the preheating / cooling unit (1
It is returned from the end of 8) to the start of the NOx adsorbing section (13) via the passage (22).
吸着剤としては、銅、バナジウム等の金属酸化物を含む
ゼオライト系吸着剤が用いられる。NOx吸着剤(13)に
おいて乾式処理によってNOx除去された処理ガスは、
煙突(26)を経て系外へ放出される。また処理ガスの一部
はブロワー(25)で予熱・冷却部(18)内を終端から始端に
向けて、すなわち移動ブロックの移動方向に対して向流
方向に流通される。その結果この処理ガスは予熱・冷却
部(18)の始端側では再生すべき吸着剤の予熱用に、また
終端側では加熱された再生吸着剤の冷却用にそれぞれ使
用される。As the adsorbent, a zeolite adsorbent containing a metal oxide such as copper or vanadium is used. The processing gas from which NOx has been removed by the dry processing in the NOx adsorbent (13) is
It is released to the outside of the system through the chimney (26). Further, a part of the processing gas is circulated in the preheating / cooling unit (18) from the terminal end to the starting end by the blower (25), that is, in the counterflow direction with respect to the moving direction of the moving block. As a result, this processing gas is used for preheating the adsorbent to be regenerated on the starting end side of the preheating / cooling section (18) and for cooling the heated regenerated adsorbent on the termination end side.
吸着剤再生部(14)においては、予熱・冷却部(18)から来
た移動ブロック(19)の未再生吸着剤がNH3 を含む高温
空気で接触処理される。この空気は循環ブロワー(15)で
吸着剤再生部(14)に送られ、かつヒーター(16)で100
℃以上に加熱される。NH3 はボンベ(17)から加熱空気
に添加される。その結果、NOxは還元剤としてのNH
3 によって窒息ガスに還元されて吸着剤から脱着し、吸
着剤が再生させられる。In the adsorbent regeneration unit (14), the unregenerated adsorbent of the moving block (19) coming from the preheating / cooling unit (18) is contact-treated with high-temperature air containing NH 3 . This air is sent to the adsorbent regeneration section (14) by the circulation blower (15), and 100% by the heater (16).
It is heated above ℃. NH 3 is added to the heated air from the cylinder (17). As a result, NOx is NH as a reducing agent.
It is reduced to asphyxiation gas by 3 and desorbed from the adsorbent, and the adsorbent is regenerated.
吸着剤再生部(14)を通過した空気は、さらに脱硝装置(2
3)でNOx除去処理され、循環ブロワー(15)で循環再使
用される。またこの空気の一部は循環ラインから抜き取
られ、前述した処理ガスの一部に熱交換器(24)で回収熱
を付与した後、煙突(26)へ放出される。他方、熱交換器
(24)で回収熱を得た処理ガスの一部は循環空気に補添さ
れる。The air that has passed through the adsorbent regeneration unit (14) is further denitrified (2
NOx removal treatment is carried out in 3), and it is circulated and reused in the circulation blower (15). Further, a part of this air is extracted from the circulation line, and after recovering heat to a part of the above-mentioned processing gas by the heat exchanger (24), it is discharged to the chimney (26). On the other hand, heat exchanger
A part of the process gas that has obtained the heat of recovery in (24) is supplemented to the circulating air.
換気ガス浄化装置の各箇所におけるガス組成および温度
は表3および表4に示すとおりである。The gas composition and temperature at each location of the ventilation gas purification device are as shown in Tables 3 and 4.
吸着剤と再生試験 径1.5mm、長さ3mmの円柱状のY型ゼオライト吸着剤
を0.1モル/とアンミン酸銅で処理し、銅イオンを
吸着担持させた。こうして得られた吸着剤75gを内径
18mmの石英製の吸着管に充填し、NOx約200ppm
と湿分約3%を含むガスを4/分で室温で連続的に吸
着管に通した。吸着管出口のNOx濃度を計測し、初期
吸着能の結果を第4図に示す。引き続いて上記NOx含
有ガスの流通を止めて、吸着剤を200℃に加熱し、2
00℃の空気を2時間吸着管に通し、吸着管出口のNO
x濃度を計測したところ、NOxはほとんど認められな
かった。これはこの条件下では吸着NOxは脱着しない
ことを示す。吸着剤を室温に冷却した後、再びNOx約
200ppm と湿分約3%を含むガスを4/分で吸着管
に通したところ、第5図に示すようにNOx吸着能はほ
とんど示されなかった。これは200℃の空気だけでは
吸着剤の再生がなされていないことを示す。 Adsorbent and regeneration test A columnar Y-type zeolite adsorbent having a diameter of 1.5 mm and a length of 3 mm was treated with 0.1 mol / mol of copper amminate to adsorb and support copper ions. 75 g of the adsorbent thus obtained was filled in a quartz adsorption tube having an inner diameter of 18 mm, and NOx was about 200 ppm.
Gas containing about 3% moisture and 4% / min was continuously passed through the adsorption tube at room temperature. The NOx concentration at the outlet of the adsorption tube was measured, and the result of the initial adsorption capacity is shown in FIG. Subsequently, the flow of the NOx-containing gas was stopped, and the adsorbent was heated to 200 ° C.
Pass the air at 00 ° C through the adsorption tube for 2 hours, and
When the x concentration was measured, almost no NOx was observed. This indicates that the adsorbed NOx does not desorb under this condition. After cooling the adsorbent to room temperature, a gas containing about 200 ppm of NOx and about 3% of moisture was passed through the adsorption tube at a rate of 4 / min. As a result, as shown in FIG. 5, almost no NOx adsorption capacity was exhibited. . This indicates that the adsorbent was not regenerated with only air at 200 ° C.
この吸着剤についで200℃に加熱し、200ppm のN
H3 を含む200℃の空気を1/分で3時間吸着管に
通した。この場合も吸着管出口のNOxはほとんど観測
されなかった。つぎにこの吸着剤を室温に冷却した後、
NOx約200ppm と湿分約3%を含むガスを4/分
で吸着管に通した。吸着管出口NOx濃度を第6図に示
す。第6図の結果は第4図の結果とほとんど同じであっ
た。したがって吸着剤はNH3 を含む200℃の空気に
よって完全に再生されたことがわかる。This adsorbent is then heated to 200 ° C. and 200 ppm N
200 ° C. air containing H 3 was passed through the adsorption tube at 1 / min for 3 hours. Also in this case, almost no NOx at the adsorption tube outlet was observed. Next, after cooling this adsorbent to room temperature,
A gas containing about 200 ppm NOx and about 3% moisture was passed through the adsorption tube at 4 / min. FIG. 6 shows the NOx concentration at the adsorption pipe outlet. The result of FIG. 6 was almost the same as the result of FIG. Therefore, it can be seen that the adsorbent was completely regenerated by the 200 ° C. air containing NH 3 .
発明の効果 この発明の換気ガス浄化方法によれば、道路トンネルか
ら出た換気ガスをゼオライト系吸着剤で乾式処理して、
主としてNOxを吸着除去し、NOx吸着状態の吸着剤
をNH3 含有高温空気で処理して再生されるので、換気
ガス中の5ppm 以下の低濃度のNOxを、換気ガスを昇
温せずに、高い効率で除去することができるとともに、
浄化設備と運転時のエネルギー消費を極力低減すること
ができる。EFFECT OF THE INVENTION According to the ventilation gas purification method of the present invention, the ventilation gas emitted from the road tunnel is dry-processed with a zeolite-based adsorbent,
Since NOx is mainly adsorbed and removed, and the adsorbent in the NOx adsorbed state is treated with NH 3 -containing high-temperature air to be regenerated, NOx having a low concentration of 5 ppm or less in the ventilation gas is heated without raising the temperature of the ventilation gas. It can be removed with high efficiency and
It is possible to reduce the energy consumption during the purification equipment and operation as much as possible.
また設備周辺への熱公害を起すおそれがない上に、浄化
に伴って廃液や固体廃棄物を生じることもない。また浄
化設備は周辺の建造物と調和する規模および形態のもの
とすることができ、必要に応じて設備全体を建屋内に収
納することもできる。In addition, there is no risk of causing heat pollution to the surroundings of the facility, and no waste liquid or solid waste is generated with purification. Further, the purification facility can be of a scale and form that is in harmony with the surrounding buildings, and the entire facility can be housed in the building if necessary.
さらに吸着剤としてはゼオライト系のものを使用するの
で、換気ガス中のNOxはもとより、各種ハイドロカー
ボン蒸気、オイルミスト等も同時に吸着除去することが
できる。Further, since a zeolite-based adsorbent is used as the adsorbent, not only NOx in the ventilation gas but also various hydrocarbon vapors, oil mist and the like can be adsorbed and removed at the same time.
第1図はこの発明の基本概念を示すフローシート、第2
図はこの発明の実施例を示すフローシート、第3図はこ
の発明の実施例で用いた換気ガス浄化設備を示す斜視
図、第4図、第5図および第6図は通ガス時間と出口N
Ox濃度の関係を示すグラフである。 (1)(11) ……トンネル、(2)(12) ……換気ブロワー、
(3) ……吸着塔、(13)……NOx吸着部、(4) ……再生
塔、(14)……吸着剤再生部、(5) ……循環ブロワー、
(6)(16) ……ヒーター、(7)(17) ……NH3 ボンベ、(1
8)……予熱・冷却部。FIG. 1 is a flow sheet showing the basic concept of the present invention, second.
FIG. 3 is a flow sheet showing an embodiment of the present invention, FIG. 3 is a perspective view showing a ventilation gas purification facility used in the embodiment of the present invention, and FIGS. 4, 5, and 6 are gas passage times and outlets. N
It is a graph which shows the relationship of Ox density. (1) (11) …… Tunnel, (2) (12) …… Ventilation blower,
(3) …… Adsorption tower, (13) …… NOx adsorption section, (4) …… Regeneration tower, (14) …… Adsorbent regeneration section, (5) …… Circulation blower,
(6) (16) …… Heater, (7) (17) …… NH 3 cylinder, (1
8) …… Preheating / cooling section.
フロントページの続き (72)発明者 鬼塚 重則 大阪府大阪市西区江戸堀1丁目6番14号 日立造船株式会社内 (56)参考文献 特開 昭49−44969(JP,A) 特開 昭50−10282(JP,A) 特開 昭53−28944(JP,A)Front Page Continuation (72) Inventor Shigenori Onizuka 1-6-14 Edobori, Nishi-ku, Osaka City, Osaka Prefecture Hitachi Shipbuilding Co., Ltd. (56) Reference JP-A-49-44969 (JP, A) JP-A-50-10282 (JP, A) JP-A-53-28944 (JP, A)
Claims (3)
以下の換気ガスを、銅および/またはバナジウムを含む
ゼオライト系吸着剤で乾式処理して、主としてNOxを
吸着除去し、NOxを吸着した吸着剤を、NH3を含む
高温空気で処理して再生させることを特徴とする、道路
トンネルにおける換気ガスの浄化方法。1. The concentration of NOx emitted from a road tunnel is 5 ppm.
The following ventilation gases are dry-treated with a zeolitic adsorbent containing copper and / or vanadium to adsorb and remove mainly NOx, and the adsorbent having adsorbed NOx is treated with high-temperature air containing NH 3 to be regenerated. A method for purifying ventilation gas in a road tunnel, which is characterized in that
着剤の再生を温度100℃以上、好ましくは150℃以
上で行なう方法。2. The method according to claim 1, wherein the adsorbent is regenerated at a temperature of 100 ° C. or higher, preferably 150 ° C. or higher.
いて、移動床式の吸着部を用いる方法。3. A method according to claim 1 or 2, wherein a moving bed type adsorption unit is used.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62313777A JPH0616813B2 (en) | 1987-12-10 | 1987-12-10 | Ventilation gas purification method in road tunnel |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62313777A JPH0616813B2 (en) | 1987-12-10 | 1987-12-10 | Ventilation gas purification method in road tunnel |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH01155933A JPH01155933A (en) | 1989-06-19 |
| JPH0616813B2 true JPH0616813B2 (en) | 1994-03-09 |
Family
ID=18045397
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP62313777A Expired - Fee Related JPH0616813B2 (en) | 1987-12-10 | 1987-12-10 | Ventilation gas purification method in road tunnel |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0616813B2 (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0722682B2 (en) * | 1989-09-29 | 1995-03-15 | 工業技術院長 | Method and apparatus for decomposing nitrogen oxides |
| DE69535054T2 (en) * | 1994-08-24 | 2007-01-04 | Ebara Corp. | Ozone generation method and methods of using the device |
| ATE230296T1 (en) * | 1996-01-24 | 2003-01-15 | Mitsubishi Materials Corp | PAVEMENT STONE FOR CLEANING NOX |
| JP2007229580A (en) * | 2006-02-28 | 2007-09-13 | Mitsubishi Heavy Ind Ltd | Method for exchanging absorbent in harmful gas removing device |
| CN113236332A (en) * | 2021-06-24 | 2021-08-10 | 青海省交通建设管理有限公司 | System for monitoring and comprehensively treating toxic and harmful gas in coal-penetrating tunnel construction period |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4944969A (en) * | 1972-09-05 | 1974-04-27 | ||
| JPS5618246B2 (en) * | 1973-06-01 | 1981-04-27 | ||
| JPS5328944A (en) * | 1976-08-27 | 1978-03-17 | Matsushita Electric Ind Co Ltd | Apparatus of cleaning air for tunnels |
-
1987
- 1987-12-10 JP JP62313777A patent/JPH0616813B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH01155933A (en) | 1989-06-19 |
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