JPH01318082A - Method for decreasing ammonia concentration of gas from coal gasification - Google Patents
Method for decreasing ammonia concentration of gas from coal gasificationInfo
- Publication number
- JPH01318082A JPH01318082A JP63148288A JP14828888A JPH01318082A JP H01318082 A JPH01318082 A JP H01318082A JP 63148288 A JP63148288 A JP 63148288A JP 14828888 A JP14828888 A JP 14828888A JP H01318082 A JPH01318082 A JP H01318082A
- Authority
- JP
- Japan
- Prior art keywords
- gas
- coal gasification
- catalyst layer
- ammonia
- concentration
- 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
Links
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 title claims abstract description 28
- 239000003245 coal Substances 0.000 title claims abstract description 23
- 238000002309 gasification Methods 0.000 title claims abstract description 17
- 229910021529 ammonia Inorganic materials 0.000 title claims abstract description 12
- 238000000034 method Methods 0.000 title claims description 6
- 230000003247 decreasing effect Effects 0.000 title abstract 2
- 239000007789 gas Substances 0.000 claims abstract description 48
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 claims abstract description 16
- 239000003054 catalyst Substances 0.000 claims abstract description 15
- 239000003638 chemical reducing agent Substances 0.000 claims abstract description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000001301 oxygen Substances 0.000 claims abstract description 6
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 6
- 238000010531 catalytic reduction reaction Methods 0.000 claims abstract description 4
- 238000011144 upstream manufacturing Methods 0.000 claims abstract description 4
- 238000006243 chemical reaction Methods 0.000 abstract description 7
- 230000007423 decrease Effects 0.000 abstract description 4
- 229910000069 nitrogen hydride Inorganic materials 0.000 abstract 2
- 239000002912 waste gas Substances 0.000 abstract 2
- 238000010586 diagram Methods 0.000 description 3
- 230000003197 catalytic effect Effects 0.000 description 2
- 238000009434 installation Methods 0.000 description 2
- ODUCDPQEXGNKDN-UHFFFAOYSA-N Nitrogen oxide(NO) Natural products O=N ODUCDPQEXGNKDN-UHFFFAOYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
Classifications
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Landscapes
- Exhaust Gas Treatment By Means Of Catalyst (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野]
本発明は石炭ガス化炉で発生するガス中に含まれるアン
モニアを低減させる方法に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a method for reducing ammonia contained in gas generated in a coal gasifier.
〔従来の技術]
石炭ガス化炉とガスタービンを組み合せた従来の設備の
一態様lr:第3図によって説明する。[Prior Art] One aspect of a conventional facility that combines a coal gasification furnace and a gas turbine will be explained with reference to FIG.
石炭ガス化炉1での反応は、還元雰囲気での反応である
ため、ガスタービン燃焼器3への経路2中の石炭ガス化
炉発生ガスはアンモニア< NHI )を多量に含んで
いる。このlaH,を多量に含んだガスをガスタービン
燃料として投入した場合、ガスタービン燃焼器3でNu
、はJIIOXになるためガスタービン排ガス配管4の
排ガス中のNOX 4度は非常に高くなり、Nowの櫨
境排出規制上好ましくない。Since the reaction in the coal gasifier 1 is a reaction in a reducing atmosphere, the gas generated from the coal gasifier in the path 2 to the gas turbine combustor 3 contains a large amount of ammonia <NHI. When gas containing a large amount of laH, is input as gas turbine fuel, the gas turbine combustor 3
, is JIIOX, so the NOX level in the exhaust gas from the gas turbine exhaust gas piping 4 becomes extremely high, which is unfavorable in terms of the Now's forest boundary emission regulations.
本発明は上記技術水準に鑑み、石炭ガス化ガス中のPi
n、を低減する合目的な方法を提供しようとするもので
ある。In view of the above-mentioned technical level, the present invention has been made to solve the problem of Pi in coal gasification gas.
The aim is to provide a purposeful method for reducing n.
〔課題を解決するための手段]
本発明は石炭ガス化炉で発生する石炭ガス化ガスの燃焼
器への供給経路に、ガス温度200〜500℃の範囲内
の経路にアンモニア?還元剤とする選択接触還元脱硝触
媒層を設け、該触媒層の前流側に窒素酸化物及び酸素含
有ガスを注入することを特徴とする石炭ガス化ガス中の
アンモニアの低減法である。[Means for Solving the Problems] The present invention provides a supply route for coal gasification gas generated in a coal gasification furnace to a combustor, in which ammonia is added to a route within a gas temperature range of 200 to 500°C. This is a method for reducing ammonia in coal gasification gas, which is characterized by providing a selective catalytic reduction denitrification catalyst layer as a reducing agent and injecting nitrogen oxide and oxygen-containing gas to the upstream side of the catalyst layer.
本発明において使用さnるアンモニアを還元剤とする選
択接触還元脱硝触媒としては、一般燃焼排ガス中のNO
Kをアンモニアを還元剤として選択的に除去する際に使
用さ几る脱硝触媒であれば任意のものが使用し得る。例
えばT10゜担体とし、活性成分としてv、W、MOl
Fe、Cu などの酸化物を担持したものが使用でき
る。The selective catalytic reduction denitrification catalyst using ammonia as a reducing agent used in the present invention is capable of reducing NO in general combustion exhaust gas.
Any denitrification catalyst that can be used to selectively remove K using ammonia as a reducing agent can be used. For example, T10° carrier and active ingredients v, W, MOL.
Those supporting oxides such as Fe and Cu can be used.
また、その触媒形状も任意のものが使用できるが、圧損
の少ないハニカム状のものを使用することが好ましい。Moreover, any shape of the catalyst can be used, but it is preferable to use a honeycomb shape with less pressure loss.
また、これら触媒層の設置位置は経路中のガス温度が2
00〜500℃がよく、特に3σ0〜450℃の範囲が
よシ好ましいことを本発明者らの実験結果によって確認
した。In addition, the installation position of these catalyst layers is such that the gas temperature in the path is 2.
The experimental results of the present inventors have confirmed that the temperature range is preferably 00 to 500°C, and particularly preferably 3σ0 to 450°C.
本発明においては石炭ガス化炉とガスタービン燃焼器の
経路のガス1211fLが200〜500℃の個所に、
上記した触媒層を設置し、その上流側に窒素酸化物(N
O)と酸素含有ガス(0,)を注入するものであるが、
これは石炭ガス化炉発生ガス中0BIB、と注入された
適量のNO及び0、t−反応させて下記式の反応により
yHs’+安定なN、に変えるためである。In the present invention, 1211fL of gas in the path between the coal gasifier and the gas turbine combustor is at a temperature of 200 to 500°C,
The above catalyst layer is installed, and nitrogen oxides (N
O) and oxygen-containing gas (0,) are injected,
This is to cause 0BIB in the gas generated by the coal gasifier to react with an appropriate amount of injected NO and 0, t- to convert it into yHs'+stable N through the reaction of the following formula.
4111i、 + 4110 + O,→41!ffi
+6馬O上記反応によシ、ガスタービン燃焼器に投入さ
れるガス中に含まれるNO,は極力低減されhに変化し
ているためガスタービン燃焼器で発生するNOxは低く
ガスタービン排ガス中のNOxは低い値となる。4111i, + 4110 + O, → 41! ffi
+6 O Due to the above reaction, the NO contained in the gas input to the gas turbine combustor is reduced as much as possible and changed to h, so the NOx generated in the gas turbine combustor is low and the amount of NOx in the gas turbine exhaust gas is NOx becomes a low value.
以下、本発明の一実施列を第1図にしたがって説明する
。第1図において、第5図と同一符号は第3図と同一部
を示す。5は石炭ガス化ガス供給経路2に設けられた窒
素酸化物(No )及び酸素含有ガス(O3)注入器、
6はアンモニアを還元剤とする選択接触脱硝触媒を充填
した反応器である。Hereinafter, one embodiment of the present invention will be explained with reference to FIG. In FIG. 1, the same reference numerals as in FIG. 5 indicate the same parts as in FIG. 3. 5 is a nitrogen oxide (No) and oxygen-containing gas (O3) injector provided in the coal gasification gas supply route 2;
6 is a reactor filled with a selective catalytic denitrification catalyst using ammonia as a reducing agent.
第1図のフローにおいて、石炭ガス化ガス中のME、に
対して、
4NEI、+4NO+O,→411.+6B、0の反応
に見合うNO及びO3を注入し、反応器6を設置した個
所の温度によって上記反応がどのように生起するかを調
べた結果を第2図に示す。In the flow shown in Fig. 1, for ME in coal gasification gas, 4NEI, +4NO+O, → 411. FIG. 2 shows the results of injecting NO and O3 corresponding to the +6B,0 reaction and investigating how the above reaction occurred depending on the temperature at the location where the reactor 6 was installed.
第2図はガス温度(反↓6器6の設置t温度)(℃)と
脱NH,率(%)との関係を示す図表でこれより反応器
6を設置する個所の温度は200〜500℃、特に50
0〜450℃の範囲内が好ましいことが判る。Figure 2 is a chart showing the relationship between gas temperature (temperature at which reactor 6 is installed) (℃) and NH removal rate (%). °C, especially 50
It turns out that the temperature within the range of 0 to 450°C is preferable.
次に、第1図の70−において、脱硝触媒を充填した反
応器6を最適温度の部位の経路2中に設置し、■0.の
み注入し、NOは注入しない場合(比較メ11)、■N
Oのみ注入し、0゜は注入しない場合(比較例2)及び
■NOと0゜の両者を注入した場合(実施列)を実施し
、下表のような結果を得た。Next, at 70- in FIG. 1, the reactor 6 filled with the denitrification catalyst is installed in the path 2 at the optimum temperature point, and (1) 0. When only injecting NO and not injecting NO (comparison method 11), ■N
A case where only O was injected and no injection at 0° was carried out (Comparative Example 2) and a case where both NO and 0° were injected (implementation row) were carried out, and the results shown in the table below were obtained.
ガスタービンに投入される石炭ガス化ガス中のNH,′
a度が低くなり、ガスタービン排ガス中の110x (
14度が低くなシ大気中に放出されるNOxが低減でき
る。NH,′ in the coal gasification gas input to the gas turbine
The degree of a decreases, and 110x (
When the temperature is 14 degrees lower, NOx released into the atmosphere can be reduced.
第1図は本発明の一実施例のフローを説明するだめの図
、第2図は本発明のアンモニアを還元剤とする選択接触
脱硝触媒層の設置位置と脱NH,率の関係を示す区民、
第3図は従来の石炭ガス化炉とガスタービンとの組合せ
設備を示す図でろる。Fig. 1 is a diagram for explaining the flow of an embodiment of the present invention, and Fig. 2 is a diagram showing the relationship between the installation position of the selective catalytic denitrification catalyst layer using ammonia as the reducing agent and the NH removal rate of the present invention. people,
FIG. 3 is a diagram showing a conventional combination equipment of a coal gasification furnace and a gas turbine.
Claims (1)
給経路に、ガス温度200〜500℃の範囲内の経路に
アンモニアを還元剤とする選択接触還元脱硝触媒層を設
け、該触媒層の前流側に窒素酸化物及び酸素含有ガスを
注入することを特徴とする石炭ガス化ガス中のアンモニ
アの低減法。A selective catalytic reduction denitrification catalyst layer using ammonia as a reducing agent is provided in a route in which the gas temperature is within the range of 200 to 500°C in a supply route of coal gasification gas generated in a coal gasifier to a combustor, and the catalyst layer A method for reducing ammonia in coal gasification gas, characterized by injecting nitrogen oxide and oxygen-containing gas into the upstream side of the coal gasification gas.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63148288A JPH083105B2 (en) | 1988-06-17 | 1988-06-17 | Ammonia reduction method in coal gasification gas. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63148288A JPH083105B2 (en) | 1988-06-17 | 1988-06-17 | Ammonia reduction method in coal gasification gas. |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH01318082A true JPH01318082A (en) | 1989-12-22 |
| JPH083105B2 JPH083105B2 (en) | 1996-01-17 |
Family
ID=15449419
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63148288A Expired - Fee Related JPH083105B2 (en) | 1988-06-17 | 1988-06-17 | Ammonia reduction method in coal gasification gas. |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH083105B2 (en) |
-
1988
- 1988-06-17 JP JP63148288A patent/JPH083105B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH083105B2 (en) | 1996-01-17 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |