JPS5821162B2 - Fluid combustion method - Google Patents

Fluid combustion method

Info

Publication number
JPS5821162B2
JPS5821162B2 JP51149864A JP14986476A JPS5821162B2 JP S5821162 B2 JPS5821162 B2 JP S5821162B2 JP 51149864 A JP51149864 A JP 51149864A JP 14986476 A JP14986476 A JP 14986476A JP S5821162 B2 JPS5821162 B2 JP S5821162B2
Authority
JP
Japan
Prior art keywords
combustion
fluidized
nox
fluidized bed
slag
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
Application number
JP51149864A
Other languages
Japanese (ja)
Other versions
JPS5375528A (en
Inventor
惇 佐々木
清通 太尾田
紀一郎 小川
健明 樋渡
真宣 竹村
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kobe Steel Ltd
Mitsubishi Heavy Industries Ltd
Original Assignee
Kobe Steel Ltd
Mitsubishi Heavy Industries Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kobe Steel Ltd, Mitsubishi Heavy Industries Ltd filed Critical Kobe Steel Ltd
Priority to JP51149864A priority Critical patent/JPS5821162B2/en
Publication of JPS5375528A publication Critical patent/JPS5375528A/en
Publication of JPS5821162B2 publication Critical patent/JPS5821162B2/en
Expired legal-status Critical Current

Links

Classifications

    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F23COMBUSTION APPARATUS; COMBUSTION PROCESSES
    • F23NREGULATING OR CONTROLLING COMBUSTION
    • F23N5/00Systems for controlling combustion
    • F23N5/003Systems for controlling combustion using detectors sensitive to combustion gas properties
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F23COMBUSTION APPARATUS; COMBUSTION PROCESSES
    • F23NREGULATING OR CONTROLLING COMBUSTION
    • F23N5/00Systems for controlling combustion
    • F23N5/003Systems for controlling combustion using detectors sensitive to combustion gas properties
    • F23N5/006Systems for controlling combustion using detectors sensitive to combustion gas properties the detector being sensitive to oxygen
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F23COMBUSTION APPARATUS; COMBUSTION PROCESSES
    • F23NREGULATING OR CONTROLLING COMBUSTION
    • F23N1/00Regulating fuel supply
    • F23N1/02Regulating fuel supply conjointly with air supply

Landscapes

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Combustion & Propulsion (AREA)
  • Mechanical Engineering (AREA)
  • General Engineering & Computer Science (AREA)
  • Fluidized-Bed Combustion And Resonant Combustion (AREA)
  • Treating Waste Gases (AREA)

Description

【発明の詳細な説明】 本発明は、流動燃焼法の改良に関し、特に、燃料として
不適当とされる各種の不良可燃物を無公害で燃焼させる
方法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an improvement in a fluidized combustion method, and in particular to a method for non-pollutingly burning various inferior combustibles that are considered unsuitable as fuel.

従来、化石燃料あるいはそれを含む可燃物やその類似物
を燃焼(焼却)する場合、該可燃物中の硫黄分や窒素分
あるいは空気中の窒素分がSOxやNOxに転化し、排
ガス中に混入して大気中に放出され、大気汚染の原因と
なっていた。
Conventionally, when fossil fuels, combustible materials containing fossil fuels, or similar materials are burned, the sulfur and nitrogen content in the combustibles, or the nitrogen content in the air, is converted to SOx or NOx, which is mixed into the exhaust gas. and was released into the atmosphere, causing air pollution.

このため、最近では、SOx、NOxの排出値が法的に
規制され、SOx、NOxの除去、抑制対策がなければ
燃焼装置の稼動は許されない情勢になって来ている。
For this reason, recently, the emission values of SOx and NOx have been legally regulated, and the situation has come such that combustion equipment cannot be operated without measures to remove and suppress SOx and NOx.

このSOx、NOxの除去、抑制対策としては、例えば
SOxについては、大規模な燃焼装置の場合、石灰石膏
法による脱硫方法、小規模な燃焼装置の場合、苛性ソー
ダによる吸収除去方法、またNOxについては、バーナ
改良や排ガス再循環等燃焼改善によるNOx発生の抑制
方法、燃焼ガスに何らかの酸化剤を添加してNOを高次
酸化物に転化後吸収除去する湿式脱硝方法、あるいはN
Oxを還元剤によりN2に環元させる乾式脱硝方法等が
開発され、実用化されつつある。
Measures to remove and suppress SOx and NOx include, for example, for SOx, a desulfurization method using the lime plaster method in the case of large-scale combustion equipment, and an absorption and removal method using caustic soda in the case of small-scale combustion equipment; , methods for suppressing NOx generation through combustion improvements such as burner improvements and exhaust gas recirculation, wet denitrification methods that add some kind of oxidizing agent to the combustion gas and absorb and remove NO after converting it into higher-order oxides;
A dry denitrification method in which Ox is reduced to N2 using a reducing agent has been developed and is being put into practical use.

しかしながら、これらの方法は、特別な専用装置を付設
する必要があり、また適用範囲(条件)が限定される等
の欠点を有している。
However, these methods have drawbacks such as the need to install special dedicated equipment and the range of application (conditions) to which they can be applied is limited.

一方、近来になって、各種の工場廃棄物例えば重油分が
付着した廃棄物や重油スラリー等形状、性状共定常性の
ない可燃物、あるいは通常の燃焼炉では安定した燃焼が
維持できない例えば集塵ダスト等の難燃性可燃物等、一
般に不良可燃物とされる可燃物を燃焼、焼却する機会が
多くなって来ている。
On the other hand, in recent years, various types of factory waste, such as waste with heavy oil adhering to it, heavy oil slurry, and other combustible materials that do not have co-constancy in shape or properties, or those that cannot maintain stable combustion in a normal combustion furnace, such as dust collection 2. Description of the Related Art There are increasing opportunities to burn and incinerate combustible materials, such as dust and other flame-retardant combustible materials, which are generally considered to be inferior combustible materials.

本発明は、上記の化石燃料あるいはそれを含む可燃物や
その類似物、および不良可燃物を無公害で燃焼させるこ
とを目的としてなされたもので、流動燃焼炉における燃
焼ガス中のSOx、NOxを容易に低減化し得る流動燃
焼法を提供するものである。
The present invention was made for the purpose of burning the above-mentioned fossil fuels, combustible materials containing them, their analogues, and defective combustible materials without causing pollution. This provides a fluidized combustion method that can easily reduce fuel consumption.

一般に、流動燃焼法では、流動層内を流動する粒子の混
合現象が極めて良好であるため、燃料は流動層内に均一
に分散され、比較的低い温度及び低い空気過剰率で燃焼
される。
In general, in the fluidized combustion method, the mixing phenomenon of particles flowing in the fluidized bed is very good, so that the fuel is uniformly dispersed in the fluidized bed and is combusted at a relatively low temperature and a low excess air ratio.

従って、サーマルNOxの発生は極めて少く、゛燃焼ガ
ス中のNOxは殆んど燃料中の窒素分によるものであり
、該NOxは還元雰囲気中で還元ガスにより容易に分解
され、N2 となり、無害化される。
Therefore, the generation of thermal NOx is extremely low, and ``NOx in the combustion gas is mostly due to the nitrogen content in the fuel, and the NOx is easily decomposed by the reducing gas in a reducing atmosphere and becomes N2, making it harmless. be done.

この時の反応は主に次の(1): 、 (2)式に示さ
れるものであるが、他にCmHnによる還元反応も含ま
れる。
The reaction at this time is mainly shown in the following formulas (1) and (2), but also includes a reduction reaction using CmHn.

2CO+2NO−)N2+2C02(1)2H2+2N
O−+N2 +2H20(2)しかしながら、燃焼炉を
還元雰囲気で操作すると、当然完全燃焼が困難になり、
悪臭ガスの発生や炭素利用率の低下等の不都合が生じる
2CO+2NO-)N2+2C02(1)2H2+2N
O-+N2 +2H20 (2) However, when a combustion furnace is operated in a reducing atmosphere, complete combustion becomes difficult,
Inconveniences such as the generation of foul-smelling gas and a decrease in the carbon utilization rate occur.

また、上記の流動媒体として石灰を用いれば、燃焼ガス
中のSOxをも容易に除去することができる。
Moreover, if lime is used as the fluidizing medium, SOx in the combustion gas can also be easily removed.

この時の反応は次のように示される。CaCO3−+
CaO+CO2(3)SO2+CaO+ 1/202
−+CaSO4(4)すなわち、石灰Ca C03は流
動燃焼炉の燃焼熱により分解されてCaOを生じ、石膏
に転換される。
The reaction at this time is shown as follows. CaCO3-+
CaO+CO2(3)SO2+CaO+ 1/202
-+CaSO4 (4) That is, lime Ca C03 is decomposed by the combustion heat of the fluidized combustion furnace to produce CaO, which is converted into gypsum.

しかし、該CaOは流動燃焼炉内で極めて微細化され易
く、大半は排ガスに伴なわれて炉外に排出されるので、
二次公害防止のために効率の良い集塵装置が必要であり
、また石灰の購入や補給の際の費用も無視できない。
However, the CaO is extremely easily atomized in the fluidized combustion furnace, and most of it is discharged outside the furnace along with the exhaust gas.
An efficient dust collector is necessary to prevent secondary pollution, and the cost of purchasing and replenishing lime cannot be ignored.

本発明は以上の周知事実に基づき、前記不良可燃物を完
全にかつ無公害で燃焼(焼却)する流動燃焼法を開発し
たものである。
The present invention is based on the above-mentioned facts and has developed a fluidized combustion method for completely burning (incinerating) the defective combustibles without causing any pollution.

すなわち本発明は、流動層の流動媒体に転炉滓又は電気
炉製鋼滓を用い、流動層の全域を均一でかつ軽微な酸化
雰囲気とし、しかも温度800〜1100℃、空気過剰
率1.15以下の条件で燃焼を行なうことを特徴とする
ものである。
That is, the present invention uses converter slag or electric furnace steel slag as the fluidized medium of the fluidized bed, provides a uniform and slightly oxidizing atmosphere throughout the fluidized bed, and has a temperature of 800 to 1100°C and an excess air ratio of 1.15 or less. It is characterized by combustion under the following conditions.

本発明における流動媒体は、製鉄工程から排出され、通
常埋立材以外にさしたる使途もない転炉滓又は電気炉製
鉄(以下、鉱滓と略す)が使用される。
The fluidizing medium used in the present invention is converter slag or electric furnace slag (hereinafter abbreviated as slag) which is discharged from the steel manufacturing process and is generally of no use other than as a landfill material.

該鉱滓は適度な粒度に粉砕可能であり、粒子硬度も充分
微細化飛出が少ない等、流動媒体として優れた特性を有
する。
The slag has excellent characteristics as a fluidizing medium, such as being able to be crushed to an appropriate particle size, and having sufficiently fine grain hardness that there is little scattering.

しかも、該鉱滓中に含まれるCa(が脱硫剤として、ま
た多種の金属酸化物が、軽微な酸化雰囲気で運転される
流動層中に出現する部分的な還元雰囲気中でNOxの分
解触媒として、更に多量の鉄分が、上記の部分的還元雰
囲気中でFeO,Fe3O4を形成して炉中に拡散しF
e2O3なる時NOxの還元剤として作用する。
Moreover, Ca contained in the slag acts as a desulfurization agent, and various metal oxides act as NOx decomposition catalysts in a partially reducing atmosphere that appears in a fluidized bed operated in a slightly oxidizing atmosphere. Furthermore, a large amount of iron forms FeO and Fe3O4 in the above partially reducing atmosphere and diffuses into the furnace.
When it becomes e2O3, it acts as a reducing agent for NOx.

本発明において、燃焼温度を800〜1100℃とした
のは、800℃以下では可燃物中の有臭成分が完全に燃
焼分解できず、炭化度の高い廃棄再燃物においては不完
全燃焼を起しCOガスの発生)率を増卯させ、1100
℃以上では燃焼生成灰が融着して流動状態を不安定化さ
せる現象が見られるからであり、同時に800〜110
0℃の温度範囲においてNOx分解が最も効果的に進行
するためである。
In the present invention, the combustion temperature is set to 800 to 1100°C because at temperatures below 800°C, odor components in combustible materials cannot be completely combusted and decomposed, and incomplete combustion occurs in waste reburned materials with a high degree of carbonization. CO gas generation) rate is increased to 1100
This is because at temperatures above 800°C to 110°C, combustion generated ash fuses and destabilizes the fluid state.
This is because NOx decomposition proceeds most effectively in the temperature range of 0°C.

また、本発明において空気過剰率を1.15以下とした
のは、これ以上の空気過剰率であると前記の部分的還元
雰囲気の生成頻度を激減しNOxの分解効果が著しく低
下するからであり、望ましくは1.1以下とする。
Further, in the present invention, the excess air ratio is set to 1.15 or less because if the excess air ratio is higher than this, the frequency of generation of the above-mentioned partial reduction atmosphere will be drastically reduced, and the NOx decomposition effect will be significantly reduced. , preferably 1.1 or less.

以下、添付の第1図を用いて本発明の実施態様を詳細に
説明する。
Hereinafter, embodiments of the present invention will be described in detail using FIG. 1 attached.

図中、1は流動燃焼炉シェル、2は流動層、3は風箱、
4は空気分散板、5は可燃物供給口、6は鉱滓投入口、
7は可燃物の燃焼残渣および鉱滓抜出口、8は温度計、
9は必要に応じて設置される伝熱手段、10はブロワ、
11はダンパ、12は酸素濃度計、13は集塵器である
In the figure, 1 is a fluidized combustion furnace shell, 2 is a fluidized bed, 3 is a wind box,
4 is an air distribution plate, 5 is a combustible material supply port, 6 is a slag input port,
7 is a combustion residue and slag extraction outlet for combustible materials, 8 is a thermometer,
9 is a heat transfer means installed as necessary; 10 is a blower;
11 is a damper, 12 is an oxygen concentration meter, and 13 is a dust collector.

本発明において、燃焼温度は、温度計8で検出し、可燃
物供給量を調節することにより、および必要に応じて伝
熱手段9にて燃焼熱を除去することにより、前記温度範
囲に制御され、また鉱滓は可燃物の特性に応じて供給量
が調節される。
In the present invention, the combustion temperature is controlled within the above temperature range by detecting it with a thermometer 8, adjusting the amount of combustible material supplied, and removing combustion heat with the heat transfer means 9 as necessary. Also, the amount of slag supplied is adjusted depending on the characteristics of the combustible material.

更に本発明では、燃焼ガス中の酸素濃度を酸素濃度計1
2で測定し、ブロワ10から風箱3に送入される空気量
をダンパ11で調節して炉内を軽微な酸化雰囲気に保つ
Furthermore, in the present invention, the oxygen concentration in the combustion gas is measured using an oxygen concentration meter 1.
2, and the amount of air sent from the blower 10 to the wind box 3 is adjusted by the damper 11 to maintain a slightly oxidizing atmosphere inside the furnace.

燃焼ガスは集塵器13にて同伴する鉱滓や燃焼残有を除
去した後大気中に放出される。
The combustion gas is discharged into the atmosphere after removing accompanying slag and combustion residue in the dust collector 13.

次に、本発明の実施例を挙げる。Next, examples of the present invention will be given.

実施例 1 直径30cmの試験用流動層に静止高さ約60cmの下
記組成の転炉滓粒子(平均粒径750μ)を充填し、平
均粒径immのコークス微粉を流動層温度900〜98
0℃、ガス空塔速度的2.4m/秒で燃焼させた。
Example 1 A test fluidized bed with a diameter of 30 cm was filled with converter slag particles (average particle size: 750 μm) having the following composition and a static height of about 60 cm, and coke fine powder with an average particle size of imm was heated at a fluidized bed temperature of 900 to 98 μm.
The combustion was carried out at 0° C. and a gas superficial velocity of 2.4 m/sec.

流動層調度は、流動層に水冷管を挿入し、その挿入度(
この挿入度によって流動層に浸漬される水冷管の伝熱面
積が変化する)で調節した。
Fluidized bed preparation involves inserting a water-cooled pipe into the fluidized bed, and adjusting the degree of insertion (
The heat transfer area of the water-cooled tube immersed in the fluidized bed changes depending on the degree of insertion.

また空気量を調整して空気過剰率を種々変化させ、燃焼
排ガス中のNOx濃度変化を測定した。
In addition, the amount of air was adjusted to vary the excess air ratio, and changes in NOx concentration in the combustion exhaust gas were measured.

この結果を第2図のグラフ1に示す。The results are shown in graph 1 of FIG.

該グラフより空気過剰率1.15以下で急激にNOx濃
度が減少することがわかる。
The graph shows that the NOx concentration decreases rapidly when the excess air ratio is 1.15 or less.

また、空気過剰率1.15以下の燃焼排ガス中のSOx
濃度は約70ppmであった。
In addition, SOx in combustion exhaust gas with an excess air ratio of 1.15 or less
The concentration was approximately 70 ppm.

また上記の転炉滓の代りに電気炉製鋼滓を用いたところ
、上記と同様の結果が得られた。
Furthermore, when electric furnace steel slag was used instead of the converter slag, the same results as above were obtained.

比較例 1 流動媒体として平均粒径800μの石灰石を用いる以外
は実施例1と同一条件で燃焼を行ない、燃焼排ガス中の
NOx濃度変化を測定した。
Comparative Example 1 Combustion was carried out under the same conditions as in Example 1, except that limestone with an average particle size of 800 μm was used as the fluidizing medium, and changes in NOx concentration in the combustion exhaust gas were measured.

この結果を第2図のグラフ2に示す。The results are shown in graph 2 of FIG.

グラフ2をグラフ1と比較すると、空気過剰率を低くし
ても実施例1のような低濃度NOx の排出は不可能で
あることがわかるであろう。
Comparing Graph 2 with Graph 1, it will be seen that even if the excess air ratio is made low, it is impossible to discharge low concentration NOx as in Example 1.

また、空気過剰率1.15以下の燃焼排ガス中のSOx
濃度は約50ppmであった。
In addition, SOx in combustion exhaust gas with an excess air ratio of 1.15 or less
The concentration was approximately 50 ppm.

実施例 2 燃焼温度800〜860℃、空気過剰率1.1とする以
外は実施例1と同一条件で平均粒径1.2mmの石炭粒
子を燃焼させた。
Example 2 Coal particles having an average particle diameter of 1.2 mm were combusted under the same conditions as in Example 1 except that the combustion temperature was 800 to 860° C. and the excess air ratio was 1.1.

燃焼排ガス中、SOX濃度:平均55ppm、NOx濃
度:平均60ppmであった。
In the combustion exhaust gas, the SOX concentration was 55 ppm on average, and the NOx concentration was 60 ppm on average.

比較例 2 流動媒体として石灰石を用いる以外は実施例2と同一条
件で燃焼を行なった。
Comparative Example 2 Combustion was carried out under the same conditions as in Example 2 except that limestone was used as the fluidizing medium.

燃焼排ガス中、SOx濃度:平均45ppm、NOx濃
度:平均130ppmであった。
In the combustion exhaust gas, the SOx concentration was 45 ppm on average, and the NOx concentration was 130 ppm on average.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は本発明の実施態様を示す概略図、第2゛図は空
気過剰率によるNOx発生量の変化を示す図表で、グラ
フ1は本発明の実施例によるもの、グラフ2は流動媒体
として石灰石を用いた比較例によるものである。
Fig. 1 is a schematic diagram showing an embodiment of the present invention, and Fig. 2 is a chart showing changes in the amount of NOx generated depending on the excess air ratio. This is based on a comparative example using limestone.

Claims (1)

【特許請求の範囲】[Claims] 1 流動燃焼炉内で再燃焼させる流動燃焼法において、
流動層の流動媒体として転炉滓又は電気炉製鋼滓粒子を
用い、該流動層内を全域に亘9均一で軽微な酸化雰囲気
とし、かつ、温度800〜1100℃、空気過剰率1.
15以下で燃焼を行うことを特徴とする流動燃焼法。
1 In the fluidized combustion method, which reburns in a fluidized combustion furnace,
Converter slag or electric furnace steel slag particles are used as the fluidized medium of the fluidized bed, and a uniform and slightly oxidizing atmosphere is maintained throughout the entire area within the fluidized bed, at a temperature of 800 to 1100°C and an air excess ratio of 1.
A fluidized combustion method characterized by combustion at a temperature of 15 or less.
JP51149864A 1976-12-15 1976-12-15 Fluid combustion method Expired JPS5821162B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP51149864A JPS5821162B2 (en) 1976-12-15 1976-12-15 Fluid combustion method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP51149864A JPS5821162B2 (en) 1976-12-15 1976-12-15 Fluid combustion method

Publications (2)

Publication Number Publication Date
JPS5375528A JPS5375528A (en) 1978-07-05
JPS5821162B2 true JPS5821162B2 (en) 1983-04-27

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Family Applications (1)

Application Number Title Priority Date Filing Date
JP51149864A Expired JPS5821162B2 (en) 1976-12-15 1976-12-15 Fluid combustion method

Country Status (1)

Country Link
JP (1) JPS5821162B2 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL182508C (en) * 1981-05-08 1988-03-16 Hoogovens Groep Bv PRESSURE CHARGED SWIRLBED COMBUSTION SYSTEM.
WO2023062988A1 (en) * 2021-10-12 2023-04-20 住友重機械工業株式会社 Boiler and co2 recovery method

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4857887A (en) * 1971-11-22 1973-08-14
JPS4994578A (en) * 1973-01-16 1974-09-07

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4857887A (en) * 1971-11-22 1973-08-14
JPS4994578A (en) * 1973-01-16 1974-09-07

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JPS5375528A (en) 1978-07-05

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