JPS62288420A - Catalytic burner - Google Patents
Catalytic burnerInfo
- Publication number
- JPS62288420A JPS62288420A JP13184186A JP13184186A JPS62288420A JP S62288420 A JPS62288420 A JP S62288420A JP 13184186 A JP13184186 A JP 13184186A JP 13184186 A JP13184186 A JP 13184186A JP S62288420 A JPS62288420 A JP S62288420A
- Authority
- JP
- Japan
- Prior art keywords
- fuel
- catalyst layer
- catalyst
- gas
- combustion
- 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.)
- Pending
Links
- 230000003197 catalytic effect Effects 0.000 title claims 4
- 239000000446 fuel Substances 0.000 claims abstract description 47
- 238000002485 combustion reaction Methods 0.000 claims abstract description 40
- 239000003054 catalyst Substances 0.000 claims abstract description 39
- 239000007789 gas Substances 0.000 claims abstract description 14
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 14
- 229910021529 ammonia Inorganic materials 0.000 claims description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 6
- MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 claims description 6
- 229910017464 nitrogen compound Inorganic materials 0.000 claims description 5
- 150000002830 nitrogen compounds Chemical class 0.000 claims description 5
- 238000006555 catalytic reaction Methods 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 claims description 3
- 238000011144 upstream manufacturing Methods 0.000 claims description 3
- 230000004913 activation Effects 0.000 claims 1
- 239000000567 combustion gas Substances 0.000 claims 1
- 238000007599 discharging Methods 0.000 claims 1
- 239000002737 fuel gas Substances 0.000 claims 1
- 238000010438 heat treatment Methods 0.000 claims 1
- 238000010248 power generation Methods 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 abstract description 12
- 238000000034 method Methods 0.000 abstract description 5
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 abstract description 4
- 230000007423 decrease Effects 0.000 abstract description 3
- 239000003345 natural gas Substances 0.000 abstract description 2
- 230000009466 transformation Effects 0.000 abstract 1
- 239000013067 intermediate product Substances 0.000 description 5
- 238000007254 oxidation reaction Methods 0.000 description 4
- 125000004429 atom Chemical group 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- 238000007084 catalytic combustion reaction Methods 0.000 description 2
- 239000013626 chemical specie Substances 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
Abstract
Description
【発明の詳細な説明】
3、発明の詳細な説明
〔産業上の利用分野〕
本発明はガスタービン用燃焼器に係り、特に、アンモニ
ア等の窒素化合物を燃焼させた場合に排出される窒素酸
化物を低減させるのに好適な燃焼器構成に関する。Detailed Description of the Invention 3. Detailed Description of the Invention [Field of Industrial Application] The present invention relates to a combustor for a gas turbine, and particularly relates to a combustor for a gas turbine, and particularly relates to a combustor for reducing nitrogen oxides emitted when nitrogen compounds such as ammonia are combusted. The present invention relates to a combustor configuration suitable for reducing combustion.
従来、主燃焼を空気不足状態で行わせ、後流で未燃分除
去のための再燃焼用空気を吹き込む、いわゆる、二段燃
焼はガス燃焼等の燃焼からのサーマルN Oxおよびフ
ューエルNOxの低減に有効であることが知られている
。また、空気を二段目に吹き込んだ場合には、吹き込み
位置がバーナ先端から遠ざかるに従って、吹き込み後の
最終NOも低下することも一般に知られている。(日本
機械学会出版燃焼に伴う環境汚染物質の生成機構と抑制
法855.12.20)即ち、燃料希薄で燃焼させると
フューエルNのNoへの変換率が高くなるので、それを
さけるために燃料過濃側で一次燃焼させ、フューエルN
からNOへの変換をおさ・え、−火燃焼で残留する未燃
成分を二次空気を混入することによって燃焼させる二段
燃焼である。Conventionally, so-called two-stage combustion, in which main combustion is performed in an air-deficient state and re-combustion air is blown in to remove unburned components in the downstream, reduces thermal NOx and fuel NOx from combustion such as gas combustion. is known to be effective. It is also generally known that when air is blown into the second stage, the final NO after blowing decreases as the blowing position moves away from the tip of the burner. (Published by Japan Society of Mechanical Engineers 855.12.20) Generation mechanism and control method of environmental pollutants associated with combustion Primary combustion is performed on the rich side, and fuel N
This is a two-stage combustion in which the unburned components remaining from the combustion are combusted by mixing secondary air, while suppressing the conversion of NO into NO.
有炎燃焼の燃焼器では可燃限界とは別に安定燃焼範囲を
もち、これ以外の範囲では不完全燃焼するか、全く火炎
を形成しなくなる。この不安定領域は燃料過濃側と燃料
希薄側にそれぞれ存在する。A flammable combustion combustor has a stable combustion range apart from the flammability limit, and outside this range, incomplete combustion or no flame is formed at all. This unstable region exists on the fuel-rich side and on the fuel-lean side, respectively.
従ってフューエルNからのNOxをおさえるために燃料
過濃で燃焼するとしても、おのずから限界がある。Therefore, even if the fuel is burnt in a rich manner in order to suppress NOx from the fuel N, there is naturally a limit.
有炎燃焼での限界値が空気過剰率に換算して0.8程度
であり、この時のフューエルNのNoχ変換率は50%
〜60%程度になる。この変換率を20%〜30%にす
るためには有炎燃焼に代る燃焼により高い燃料過濃条件
を作らなければならない。The limit value for flaming combustion is about 0.8 when converted to excess air ratio, and the Noχ conversion ratio of fuel N at this time is 50%.
It will be about 60%. In order to achieve this conversion rate of 20% to 30%, it is necessary to create highly fuel rich conditions by combustion instead of flaming combustion.
本発明は従来の燃焼器が有炎燃焼であるために燃料過濃
状態で燃焼できる範囲が限られており、フューエルNの
N Ox変換率をなかなか下げることができないという
問題があった。The present invention has a problem in that because the conventional combustor uses flaming combustion, the range in which it can burn in a fuel-rich state is limited, and it is difficult to lower the NOx conversion rate of fuel N.
本発明の目的はより高い燃料過濃状態を作り出し、しか
も、安定して燃焼するような燃焼器構造を提供すること
にある。An object of the present invention is to provide a combustor structure that can create a higher fuel enrichment state and achieve stable combustion.
従来の触媒燃焼は燃料希薄状態で使用されることが多く
燃焼上からは特に問題はない。即ち、燃料のまわりには
十分な酸素が存在し、しかも触媒上で酸化反応が進むた
めにその部分は高温になり、火炎の安定性もよくなる。Conventional catalytic combustion is often used in fuel lean conditions, and there are no particular problems from a combustion standpoint. That is, there is sufficient oxygen around the fuel, and since the oxidation reaction progresses on the catalyst, the temperature in that area becomes high and the flame stability improves.
一方、本発明では燃料過濃状態で触媒を使用するため、
触媒だけでは燃料と酸素の十分な混合は期待できず、従
って、反応温度も上昇しない。On the other hand, in the present invention, since the catalyst is used in a fuel rich state,
Sufficient mixing of fuel and oxygen cannot be expected with the catalyst alone, and therefore the reaction temperature will not increase.
本発明はこの状態でも反応が進み、i終的には低NOx
、高効率の燃焼システムを作ることにある。The present invention allows the reaction to proceed even in this state, ultimately resulting in low NOx
, to create a highly efficient combustion system.
上記の目的を達成するために1次のような燃焼経過をと
る。燃料過濃状態の予混合気を部分酸化するために設け
られた触媒中で燃焼させ、そこでのフューエルNからN
Oxへの変換をおさえる。In order to achieve the above objective, the combustion process is as follows. The fuel-rich premixture is combusted in a catalyst provided for partial oxidation, and the fuel N to N
Prevents conversion to Ox.
一方、この触媒反応から生成されるガスはC02HCな
どの未燃分を多く含むために、この触媒下流に別に設け
られた触媒によって完全燃焼する。On the other hand, since the gas generated from this catalytic reaction contains a large amount of unburned components such as CO2HC, it is completely combusted by a catalyst separately provided downstream of this catalyst.
部分酸化用触媒反応では燃焼反応を持続するための熱が
期待できないために、別に触媒上流に熱源を設け1部分
反応をたすける。Since heat to sustain the combustion reaction cannot be expected in the partial oxidation catalytic reaction, a separate heat source is provided upstream of the catalyst to facilitate the partial reaction.
燃焼器頭部に設けられたパイロットバーナは第一段の触
媒を加熱し、さらに、予混合燃料の部分酸化に必要な熱
を供給する。A pilot burner located at the head of the combustor heats the first stage catalyst and also provides the heat necessary for partial oxidation of the premixed fuel.
第一段の触媒は燃料過濃な予混合気を部分酸化し、主に
UHCに変換する。また、燃料中に含まれる窒素分をシ
アン、あるいは、アンモニアに変換する。The first stage catalyst partially oxidizes the fuel-rich premixture and converts it mainly into UHC. It also converts nitrogen contained in the fuel into cyanide or ammonia.
第二段の触媒は、第一段の触媒反応で生成されるUCH
lあるいは、coを完全燃焼する。The second stage catalyst is UCH produced in the first stage catalytic reaction.
Completely burn l or co.
第1図は燃焼器の基本原理を示す。燃焼器頭部のプリバ
ーナで予混合気と触媒Aを加熱し触媒Aでの部分燃焼を
補助する。供給される予混合気は空気過剰率に換算して
λ=0.5以下となる。燃料中に含まれるアンモニア等
の窒素成分は、触媒Aを通過する過程で、シアンとアン
モニアに分解し、他の可燃成分、たとえば、Hzt C
H4,C0などは一酸化炭素、未燃のハイドロカーボン
に分解排出される。一般に、アンモニア等を含むフュー
エルNがN Oxに変換する過程は反応帯で分解し、N
原子を含む中間生成物を生じ、中間生成物は0M子を含
む化学種と反応してNOとなるが、又は、中間生成物は
NOと反応してNoを分解し。Figure 1 shows the basic principle of a combustor. A preburner at the head of the combustor heats the premixture and catalyst A to assist partial combustion in catalyst A. The supplied premixture has an excess air ratio of λ=0.5 or less. Nitrogen components such as ammonia contained in the fuel are decomposed into cyanide and ammonia in the process of passing through catalyst A, and other combustible components such as HztC
H4, CO, etc. are decomposed and discharged into carbon monoxide and unburned hydrocarbons. Generally, the process in which fuel N containing ammonia etc. is converted to NOx is decomposed in a reaction zone and N
An intermediate product containing the atom is produced, and the intermediate product reacts with a species containing 0M atoms to form NO, or the intermediate product reacts with NO to decompose the NO.
N2になる経路をとる。ここで、○原子を含む化学種は
OHラジカル等である。又、中間生成物はN Hz 、
N Hl又は、Nが考えられる。一般には、フューエ
ルNがNHz 、NH,Nなどの中間生成物に分解が進
んだ後のO原子を含む化学種との反応がフューエルNo
生成を支配することになる。Take the route that leads to N2. Here, the chemical species containing the ○ atom are OH radicals and the like. Also, the intermediate product is N Hz,
N Hl or N can be considered. In general, the reaction between fuel N and chemical species containing O atoms after the decomposition of fuel N into intermediate products such as NHZ, NH, and N is known as fuel no.
It will control generation.
このことは火炎の性質が主な支配要因となることをあら
れしている。一般に、燃焼温度が下るほど排出されるN
o濃度は減少することがわかっている。そこで火炎の温
度を均一にし、なお火炎温度の低い状態を作る必要があ
る。触媒燃焼はこの二つの事項を満足する。This suggests that the nature of the flame is the main controlling factor. Generally, the lower the combustion temperature, the more N is emitted.
o concentration is known to decrease. Therefore, it is necessary to equalize the flame temperature and create a low flame temperature condition. Catalytic combustion satisfies these two requirements.
触媒下流は段階的に導入される空気と触媒で部分酸化さ
れて生成された未燃のガスが混合し、ここでは希薄混合
気となって段階的に完全燃焼に移行するにの完全燃焼室
は有炎燃焼で行う場合と、ここに触媒を用いる場合等が
考えられる。いづれの場合も作用としては同一である。Downstream of the catalyst, the air that is introduced in stages is mixed with unburned gas that is partially oxidized by the catalyst. Here, the mixture becomes a lean mixture, and the complete combustion chamber moves to complete combustion in stages. Possible methods include flaming combustion and using a catalyst. The effect is the same in either case.
第2図に燃焼器の一実施例を示す。パイロットバーナ1
は燃焼器ライナ4の頭部に設けられる。FIG. 2 shows an embodiment of the combustor. Pilot burner 1
is provided at the head of the combustor liner 4.
ここに使われる燃料は油、又は天然ガス等が考えられ、
主燃料とは異なる。予混合気ノズル2はフューエルNを
含む燃料と空気過剰率換算で0.5以下となるような予
混合気はライナ内に供給する。The fuel used here can be oil, natural gas, etc.
Different from main fuel. The premixture nozzle 2 supplies a premixture containing fuel including fuel N and a premixture having an excess air ratio of 0.5 or less into the liner.
供給された予混合気はパイロットバーナで予熱され、下
流の触媒3に導かれる。触媒3では予熱された燃料が部
分酸化し、下流の燃焼室5に導かれる。触媒下流のライ
ナからは、途中、段階的に空気が導入され、空気過剰率
が増加しながら完全燃焼する。The supplied premixture is preheated by a pilot burner and guided to the catalyst 3 downstream. In the catalyst 3, the preheated fuel is partially oxidized and guided to the downstream combustion chamber 5. Air is introduced in stages from the liner downstream of the catalyst, and complete combustion occurs as the excess air ratio increases.
本発明によれば、フューエルNを含む燃料を燃料過濃な
状態で安定して燃焼できるので、フューエルNからN
Oxへの変換率を小さくすることができ、しかも、触媒
後流で希薄燃焼による完全燃焼ができるので、低NOx
、高効率の燃焼器となる。According to the present invention, it is possible to stably burn fuel containing fuel N in a fuel-rich state.
The conversion rate to Ox can be reduced, and complete combustion can be achieved through lean combustion downstream of the catalyst, resulting in low NOx
, resulting in a highly efficient combustor.
Claims (1)
ービン発電装置で、前記燃焼器は燃料及び空気の供給口
と燃焼ガスを排出する出口をもつ燃焼室を備え、前記燃
焼室は流路を構成し、前記流路内に触媒反応層と、触媒
層、あるいは、前記燃料と空気の予混合気を加熱するた
めの燃焼器を収容し、前記流路は前記触媒層によつて複
数の空間に区別され、前記触媒層の上流のガスは全て前
記触媒層を経て前記触媒層下流の空間に達し、前記触媒
層上流の空間はアンモニア等の前記窒素化合物を含む燃
料と空気を混合するための空間となり、前記触媒層の下
流の空間は前記触媒層における触媒作用によつて生成さ
れるガスを完全燃焼させるための空間となり、この空間
には完全燃焼のために必要な空気が供給され、前記触媒
層では前記窒素化合物を含む燃料と空気の混合ガスを触
媒作用で活性化し、前記触媒層に供給される混合気濃度
を空気過剰率換算で0.5以下とし、さらに、前記触媒
層での活性化温度がアンモニアから前記窒素酸化物に変
換しない1000℃以下の温度に制限し、前記触媒層よ
り下流の空間では前記触媒層で生成されたシアン等の窒
素化合物を窒素と水に分解できるような温度となるよう
に空気量制御を行うことを特徴とする触媒燃焼器。1. A gas turbine power generation device equipped with a combustor for fuel gas containing nitrogen compounds, wherein the combustor includes a combustion chamber having a fuel and air supply port and an outlet for discharging combustion gas, and the combustion chamber has a flow path. and a catalytic reaction layer and a combustor for heating the catalyst layer or the premixture of fuel and air are accommodated in the flow path, and the flow path is formed by the catalyst layer to form a plurality of All the gas upstream of the catalyst layer passes through the catalyst layer and reaches the space downstream of the catalyst layer, and the space upstream of the catalyst layer is for mixing air with fuel containing the nitrogen compound such as ammonia. The space downstream of the catalyst layer is a space for complete combustion of the gas generated by the catalytic action in the catalyst layer, and air necessary for complete combustion is supplied to this space, In the catalyst layer, the mixture gas of fuel and air containing the nitrogen compound is activated by a catalytic action, and the concentration of the mixture supplied to the catalyst layer is set to 0.5 or less in terms of excess air ratio; The activation temperature is limited to a temperature of 1000°C or less at which ammonia is not converted into the nitrogen oxides, and in the space downstream from the catalyst layer, nitrogen compounds such as cyanide generated in the catalyst layer can be decomposed into nitrogen and water. A catalytic combustor characterized by controlling the amount of air so that the temperature is maintained.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13184186A JPS62288420A (en) | 1986-06-09 | 1986-06-09 | Catalytic burner |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13184186A JPS62288420A (en) | 1986-06-09 | 1986-06-09 | Catalytic burner |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS62288420A true JPS62288420A (en) | 1987-12-15 |
Family
ID=15067351
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP13184186A Pending JPS62288420A (en) | 1986-06-09 | 1986-06-09 | Catalytic burner |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62288420A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04227416A (en) * | 1990-04-16 | 1992-08-17 | General Electric Co <Ge> | Gas-turbine catalyst combustion apparatus with pre-burner reducing quantity of nox generated |
JP2006118854A (en) * | 2004-10-20 | 2006-05-11 | United Technol Corp <Utc> | Method and system for rich-lean catalytic combustion |
-
1986
- 1986-06-09 JP JP13184186A patent/JPS62288420A/en active Pending
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04227416A (en) * | 1990-04-16 | 1992-08-17 | General Electric Co <Ge> | Gas-turbine catalyst combustion apparatus with pre-burner reducing quantity of nox generated |
JP2591866B2 (en) * | 1990-04-16 | 1997-03-19 | ゼネラル・エレクトリック・カンパニイ | Gas turbine catalytic combustor with preburner with reduced NOx generation |
JP2006118854A (en) * | 2004-10-20 | 2006-05-11 | United Technol Corp <Utc> | Method and system for rich-lean catalytic combustion |
US7444820B2 (en) | 2004-10-20 | 2008-11-04 | United Technologies Corporation | Method and system for rich-lean catalytic combustion |
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