JPS58207939A - Gasification of sulfur-containing fuel - Google Patents

Gasification of sulfur-containing fuel

Info

Publication number
JPS58207939A
JPS58207939A JP8245183A JP8245183A JPS58207939A JP S58207939 A JPS58207939 A JP S58207939A JP 8245183 A JP8245183 A JP 8245183A JP 8245183 A JP8245183 A JP 8245183A JP S58207939 A JPS58207939 A JP S58207939A
Authority
JP
Japan
Prior art keywords
sulfur
fuel
layer
item
gasification
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
Application number
JP8245183A
Other languages
Japanese (ja)
Inventor
ア−ネスト・エル・ダマン
ピ−タ−・ステイナ−
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.)
Foster Wheeler Inc
Original Assignee
Foster Wheeler Inc
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 Foster Wheeler Inc filed Critical Foster Wheeler Inc
Publication of JPS58207939A publication Critical patent/JPS58207939A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J3/00Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
    • C10J3/46Gasification of granular or pulverulent flues in suspension
    • C10J3/54Gasification of granular or pulverulent fuels by the Winkler technique, i.e. by fluidisation
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/18Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles
    • B01J8/24Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles according to "fluidised-bed" technique
    • B01J8/32Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles according to "fluidised-bed" technique with introduction into the fluidised bed of more than one kind of moving particles
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J3/00Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
    • C10J3/46Gasification of granular or pulverulent flues in suspension
    • C10J3/48Apparatus; Plants
    • C10J3/482Gasifiers with stationary fluidised bed
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J3/00Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
    • C10J3/72Other features
    • C10J3/74Construction of shells or jackets
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2200/00Details of gasification apparatus
    • C10J2200/36Moving parts inside the gasification reactor not otherwise provided for
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00Details of gasification processes
    • C10J2300/09Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
    • C10J2300/0913Carbonaceous raw material
    • C10J2300/093Coal
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00Details of gasification processes
    • C10J2300/09Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
    • C10J2300/0953Gasifying agents
    • C10J2300/0956Air or oxygen enriched air
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00Details of gasification processes
    • C10J2300/09Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
    • C10J2300/0953Gasifying agents
    • C10J2300/0973Water
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00Details of gasification processes
    • C10J2300/09Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
    • C10J2300/0983Additives
    • C10J2300/0996Calcium-containing inorganic materials, e.g. lime
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00Details of gasification processes
    • C10J2300/18Details of the gasification process, e.g. loops, autothermal operation
    • C10J2300/1846Partial oxidation, i.e. injection of air or oxygen only

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 (背景技術) 本発明rat−イオウ含肩含料燃料ス化に関し、特に、
粒子材料から成る流動層ケ用いてガス化を行なう方法に
関する。
DETAILED DESCRIPTION OF THE INVENTION (Background Art) The present invention relates to the production of rat-sulfur-containing fuel, in particular:
This invention relates to a method for gasification using a fluidized bed made of particulate material.

環境庁及び各種の国家愼関は化石燃料を便用する発電所
に対し、最大許容二酸化イオウの排出水準を定めた実行
基準を制定した、この基準に対応して、排ガス浄化装置
tつくり、ボイラー排ガスが大気中に放散する前に核ガ
スから二酸化イオウを除去することが計画されている。
The Environment Agency and various national authorities have established implementation standards that set maximum allowable sulfur dioxide emission levels for power plants that use fossil fuels. It is planned to remove sulfur dioxide from nuclear gases before the exhaust gases are dissipated into the atmosphere.

しかし、希薄濃度の二酸化イオウを富む大量のガスがボ
イラーの出口に県中するので、排ガス浄化装置は大きく
なり、高1曲になる。
However, because a large amount of gas enriched with dilute sulfur dioxide flows into the boiler outlet, the exhaust gas purification equipment becomes large and has a high capacity.

スタックからの排ガスを処理して二酸化イオウの放出量
を制御するよシも、燃料がボイラーで燃焼する前に脱硫
する方が、処理に必要なガスの体積が憔めてりなくなる
点において有利である。
Although it is possible to treat the exhaust gas from the stack to control the amount of sulfur dioxide released, it is advantageous to desulfurize the fuel before it is combusted in the boiler because the volume of gas required for treatment is reduced. be.

この目的のために、燃料のがス化処理の技術が@発され
て2す、この処理では石灰粒子のf#、勤層で燃料、た
とえば重油あるいは、粒状石炭の部分燃焼を伴う。脱硫
は、石灰粒子との反応を通じて行なわれ、生成された可
燃性オフガスは、例えば市販のがスパーカを用いて燃焼
させるボイラーのような外部装置で用いられる、 このような装置では、流動層温度が7!r00 ”F(
El!; ℃)  から1too″F (t7/ ℃)
の範囲に制御されるならば、最大の脱硫効率が得られ、
温度が/1,00 ? (g7/ ℃)を越えると石灰
のイオウ保持力は急速に低下する。しかし、この比較的
低い温度ではガス化処理の効率に限度があり、工業的実
用的速度で運転することは困鼎である7(本発明の概要
) 従って、本発明の目的は、化学的活性のある流動層を提
供し、はとんどイオウ分のない生成ガスをつくるfス化
方法を提供することである。
For this purpose, the technology of fuel gasification treatment has been developed2, which involves the partial combustion of a fuel, such as heavy oil or granular coal, in the f#, formation layer of lime particles. Desulfurization is carried out through reaction with lime particles, and the combustible off-gas produced is used in an external device, such as a commercially available sparker-fired boiler. 7! r00”F(
El! ;℃) to 1too″F (t7/℃)
Maximum desulfurization efficiency can be obtained if the desulfurization efficiency is controlled within the range of
The temperature is /1,00? (g7/°C), the sulfur retention capacity of lime decreases rapidly. However, at this relatively low temperature, there is a limit to the efficiency of the gasification process, making it difficult to operate at an industrially practical speed. The object of the present invention is to provide a fluidized bed that is free of sulfur, and to provide a process for producing sulfur that produces a product gas that is virtually free of sulfur.

さらに本発明の目的は、脱硫を低下させずにガス化処理
を極めて高い温度で行うことができる上述の形式の方法
を提供することである。
Furthermore, it is an object of the invention to provide a process of the above-mentioned type in which the gasification process can be carried out at very high temperatures without reducing the desulfurization.

さらに、本発明の目的に、カルシウムを含む粒子材料か
ら成る流動層を提供し、生成ガスのイオウと反応させる
上述の形式の方法を提供するこ゛とである。
Furthermore, it is an object of the present invention to provide a process of the type described above, in which a fluidized bed consisting of particulate material containing calcium is reacted with the sulfur of the product gas.

さらに本発明の目的は、粒子材料がシリyyを含んでお
り、これによって、処理温度を比較的高い櫃に保持する
ことができ、脱硫を減少させずにがス化効率を向上させ
ることができる上述の形式の方法を提供することである
A further object of the present invention is that the particle material contains silicate, which allows the processing temperature to be maintained at a relatively high temperature and improves the desulfurization efficiency without reducing desulfurization. The object of the present invention is to provide a method of the type described above.

本発明の方法によれば、粒子材料から成る流動層を形成
し、この粒子材料は燃料がガス化したとき発生するイオ
ウと反応するカルシウムを含んでいるっまた、流動層に
は、シリカが含まnており、これによシイオウ分回収の
減少tfPなうことなしにがス化効率を向上させる温度
で流動層を運転することができる。
According to the method of the present invention, a fluidized bed of particulate material is formed, which particulate material contains calcium that reacts with the sulfur produced when the fuel is gasified, and the fluidized bed also contains silica. This allows the fluidized bed to be operated at temperatures that improve sulfur conversion efficiency without reducing tfP recovery.

本発明J〕上述の説明及び目的、特徴及び利点は添付の
図面に関連して不発明に促う好まし%A実施例の以下の
詳細な説明を参照して十分に理解さnるだろう。
The foregoing description and objects, features and advantages will be better understood by reference to the following detailed description of preferred embodiments of the invention in conjunction with the accompanying drawings. .

(実施例の説明J 本発明のItI#黴を第1図及び第2図に示されるガス
化装置10を参照にしつつ説明する。
(Explanation of Examples J) The ItI# mold of the present invention will be described with reference to the gasification apparatus 10 shown in FIGS. 1 and 2.

ガス化!i[10d、への6いた床すなわち、格子12
、前部壁14、後部壁11、及び格子12から屋根18
にわたって延びるコクの側壁17(第2図参照)とを備
えている。垂直部20が前部&!!14と後部壁16と
の間を延びて、がス化装ritoの内部をが黒化部22
と再生部24とに分割している。床12、壁14及び1
6、屋根18及び垂直部20riすべて周知の方法で断
熱処理されている。
Gasification! i[10d, i.e. the grid 12
, front wall 14, rear wall 11, and lattice 12 to roof 18
It is provided with a full-bodied side wall 17 (see FIG. 2) extending over the entire length. The vertical part 20 is the front part &! ! 14 and the rear wall 16 to cover the inside of the gas cover.
and a reproduction section 24. floor 12, walls 14 and 1
6. The roof 18 and the vertical portion 20ri are all heat-insulated using a well-known method.

空気ダクト26が床の下に延び、該ダクト26は外部か
ら空気を受は入れる入口28を有している。複数のT形
空気分配管装置30が床を貫通して延び、該装置30r
i、ダクト26から空気を受は入れ該空気IFス化部2
2及び再生部24に導入する。第2図によく表わされて
いるように、各管襞fl130は床12の開口を通して
延びる垂直管3Uaと該垂直管に接続され、そこから空
気を受け入れる水平gaobを備えている。図示されて
いないが、水平管30bはその上g表面に形成さルた一
連の一ロケMしており、空気をガス化部22及び再生部
24に分配するようになっている。
An air duct 26 extends below the floor and has an inlet 28 for receiving air from outside. A plurality of T-shaped air distribution piping devices 30 extend through the floor, the devices 30r
i. Air is received from the duct 26 and the air IF converter 2
2 and the reproduction section 24. As best seen in FIG. 2, each tube fold fl 130 includes a vertical tube 3Ua extending through an opening in the floor 12 and a horizontal gaob connected to the vertical tube and receiving air therefrom. Although not shown, the horizontal pipe 30b has a series of holes M formed on its upper surface to distribute air to the gasification section 22 and the regeneration section 24.

複数の燃料分配管裂櫨32が床12の他の開口を貫通し
てガス化s24の丁万に延び、該慾科分配管装f1t、
32の谷々は床12のf方に延びる水平管32aと床を
貫通して処び水平t、Haと連結された垂!’f32b
t−備えてする。
A plurality of fuel distribution piping holes 32 extend through other openings in the floor 12 to the gasification s24, and the fuel distribution piping system f1t,
The valleys of 32 pass through the horizontal pipe 32a extending in the f direction of the floor 12, and are connected to the horizontal pipes t and Ha. 'f32b
t- Prepare.

谷水乎管32aの端部は、それぞれlII壁17を通し
て延び石油または粒状石炭等の燃料源(図示せず>VC
毅続されるようになっている。
The ends of the valley water pipes 32a each extend through the II wall 17 and connect to a fuel source (not shown) such as petroleum or granulated coal.
It is becoming more persistent.

供給装置346・ま、肯壁17を遡して延びカルシウム
及びシリカを含む粒子材料t−ガス化部分22に供給す
るようになっている。例えば、材料は以下に示すat瀘
組成つポルトランドセメントの組成を有するもつでも艮
い。
A supply device 346 extends back up the wall 17 and supplies particulate material containing calcium and silica to the gasification section 22. For example, the material may have the following composition: Portland cement.

CaO6θ〜l、591 M2036% Fi20:s       J% 5LO2−2/〜26% Na2O/  慢 5032  % MgO,2% 上述の組成の中にシリカが存在することにより、予期し
ない結果が生じ、イオウ回収の減少を伴なわずに、シリ
カを含まない組成のものを使用する場廿よりも高い温度
でガス化処理を行うことができる。
CaO6θ~l, 591 M2036% Fi20:s J% 5LO2-2/~26% Na2O/ 5032% MgO, 2% The presence of silica in the above-mentioned composition causes unexpected results and impedes sulfur recovery. The gasification process can be carried out at higher temperatures than when using silica-free compositions without loss.

カルシウムおよびシリカを含む組成物は、上述の特定の
実施例に限定されるものではない。すなわち、イオウと
反応して水素−イオウガスから所定tのイオウを除去す
る所要のカルシウム量に対して、十分なシリ″力が存在
して、単に石灰あるいは石灰岩を用いるだけの同様な処
mを行なう4I&よりも、高温でイオウの回収の減少を
伴なわずにがス化処理を行う、ことができるかぎり、上
記組成−′:。
Compositions containing calcium and silica are not limited to the specific examples described above. That is, for the amount of calcium required to react with sulfur and remove a given amount of sulfur from the hydrogen-sulfur gas, sufficient silicate power exists to perform a similar treatment using only lime or limestone. 4I & the above composition -': as long as it is possible to carry out the sulfur treatment at higher temperatures without reducing the recovery of sulfur.

物は変良できる。例えば、別の組成物として、粒子材料
は上、述のものとほぼ同じ割合のカルシウムとシリカの
混合物から構成されてもよいっカルシウム及びシリカを
含む材料は、ガス化部22に導入さ!しる前に、例えば
、水を導入して回転ディヌク、スクリーン等を用−て、
球あるいはイレット状にかためることが好ましい。これ
によって、材料の操作性が艮くなシ、処理効率が同上す
る。
Things can change. For example, as an alternative composition, the particulate material may be comprised of a mixture of calcium and silica in approximately the same proportions as described above. For example, by introducing water and using a rotating dinuk, screen, etc.,
It is preferable to harden into a ball or an islet shape. This improves processing efficiency without impairing material handling.

がス化部22には、+111壁36が設けられており、
該分離壁36riがスIt、部分22をチャンノ(22
a及び22I)に分割している(第2図参照)。
The gas conversion part 22 is provided with a +111 wall 36,
The separation wall 36ri connects the section 22 to the channel (22).
a and 22I) (see Figure 2).

分離壁36は、仕切り20から後部壁16の陰几た鎖酸
まで煤びており、チャンノ< 22 aと22bを連絡
する通路22cを形成している。
The separation wall 36 extends from the partition 20 to the dark chain acid of the rear wall 16 and forms a passageway 22c connecting the channels 22a and 22b.

人口スロット38と出口スロット40が仕切り20に杉
成さnて29、人口スロット38はチャンバ22aと再
生部24を1!!絡し、出口スロット4(IX、チャン
バ22t)と再生$24とを連絡してい6゜ このように配置した結果、供紺装fi34を介してガス
化部22に導入された粒子材料と、燃料分配置tg*a
zを介してガス化部22に導入された燃料(例えばオイ
ル)とは混合され、チャン・シ22bを通る通路22c
及びスロット38を通ってチャンバ22bから再生部2
4に連続的に流れ込み、その舛生部24からスロット4
0を通してチャンバ22bに流れ込んで再循環する。
The population slot 38 and the exit slot 40 are connected to the partition 20 (29), and the population slot 38 connects the chamber 22a and the regeneration unit 24 to 1! ! As a result of this arrangement, the particulate material introduced into the gasification section 22 via the feeder fi 34 and the fuel Distribution tg*a
The fuel (for example, oil) introduced into the gasification section 22 through the gasification section 22b is mixed with a
and the regeneration section 2 from the chamber 22b through the slot 38.
4 continuously flows into the slot 4 from its bulge 24.
0 into chamber 22b for recirculation.

一対の出口42及び44が屋根18に設けられており、
これらの出口はガス化部分22及び再生部24の上部に
連絡しており、それぞれq!r部で生成さ几た生成fス
及びイオウガスを排出するようになっている。
A pair of outlets 42 and 44 are provided in the roof 18;
These outlets communicate with the upper part of the gasification section 22 and the regeneration section 24, each with q! The sulfur gas and sulfur gas produced in the r section are discharged.

装置の運転においては、一定量の粒子材料がガス化部2
2に配置される。そして、層の温度は燃料分配f装置3
2から層に入る燃料を制御することによ)はぼ9g0℃
(1g00ア)に保持される。
In operation of the device, a certain amount of particulate material enters the gasification section 2.
It is placed in 2. And the temperature of the layer is the fuel distribution f device 3
By controlling the fuel entering the layer from 2) is approximately 9g0℃
(1g00a).

ダクト26から空気が化学を論以下の割合で空気分配!
装置30を通してガス化部に導入され、該空気は層材料
を流動化させ、燃焼及び発熱量を抑える。一方、排煙を
不活性の熱吸収媒体として使用し、処理温度が高くなり
過ぎないように制御している。
Air is distributed from duct 26 at a rate below chemistry!
Introduced into the gasification section through device 30, the air fluidizes the bed material and reduces combustion and heat generation. On the other hand, flue gas is used as an inert heat-absorbing medium to control the processing temperature so that it does not become too high.

燃料と空気の導入量をc1!!整することにより、ガス
化$22で化学量論的に約2!;’laから30%のり
気と燃料が部分燃−し、この燃焼は燃料を部分燃焼させ
るのに十分な熱を供電し、さらに、場合によっては、残
りのオイルを蒸発させたり分解する。
The amount of fuel and air introduced is c1! ! By adjusting the gasification rate, the stoichiometry is approximately 2 at a gasification rate of $22! ;'la to 30% of the fuel and the fuel is partially combusted, and this combustion provides enough heat to partially combust the fuel and optionally vaporize or decompose the remaining oil.

この部分燃焼によ#)硫化水素が形成され、硫化水素は
層材料中のカルシウムと反応して硫化カルシウムを形成
する。この処理のがス生成物は実質的に、イオウ及びパ
ナゾウム°のない燃料ガスであり、はぼ200 sTU
/ft3(1,,7ジユ一ル/m”)の発熱tfI:有
する。このガスは、自然対流によシガス化$22=i上
昇し、出口4zを通ってガス化装置から出て、ゲイラー
等の外部装置への通路に送られる。
This partial combustion forms hydrogen sulfide, which reacts with calcium in the layer material to form calcium sulfide. The gas product of this process is essentially sulfur- and panazum-free fuel gas, with approximately 200 sTU
/ft3 (1,7 units/m") of heat generation tfI: This gas rises by natural convection, exits the gasifier through outlet 4z, and enters the gaylor. and other external devices.

ダクト26からの空気は、空気分配管装置30を逃して
再生部z4にも導入され、雰囲気を酸素リツナ$態にす
る。ガス化部22で形成された硫1′ヒフJルシウムは
、上述のように再生$24i通して循環さtl−る 再
生部24は所定の高温(別えば応に征い、硫化カルシウ
ムが、高い二酸化イオウ濃度のオフガスを発生しつつ、
酸化力ルシウムラムに変化する。
The air from the duct 26 escapes the air distribution piping device 30 and is also introduced into the regeneration section z4, making the atmosphere oxygen-rich. The sulfurized lucium formed in the gasification section 22 is circulated through the regeneration section 24i as described above. While generating off-gas with sulfur dioxide concentration,
Oxidizing power Changes to lucium rum.

Ca5O+ CaS + 02→JCaO+ 、2S0
2上述の反応によシ生成する二酸化イオウは再生部24
から出口44を通して排出され、外部装置によりがス流
れの中から元素イオウの形で回収される。一方、酸化カ
ルシウムは再循環されてガス化部22に尖されイオウ吸
収剤として再使用される。
Ca5O+ CaS + 02→JCaO+, 2S0
2 The sulfur dioxide produced by the above reaction is transferred to the regeneration section 24.
is discharged from the gas through outlet 44 and recovered from the gas stream in the form of elemental sulfur by an external device. On the other hand, the calcium oxide is recycled to the gasification section 22 and reused as a sulfur absorbent.

ドレン管等(図示せず)を通して、反応源みのl−材料
を連続的に除去′すると共に供給装置34を通してl−
材料を補充することによシがス化部22におけるイオウ
保持力が、維持される。必要な粒子材料の量はガスから
除去されるべきイオウの量にムロじて変化する。、この
ノー材料の量は、!−に投入する粒子材料の量と、層か
ら除去する反応源み材料のtを変えることによってII
I Mすることができるつ 上述′f)結果として、層材料の中にカルシウムが存在
することにより、実質的にイオウの存任しなり一1主成
fス勿効率艮く発生さぜることができ、一方、ノリ刀の
存在シこよって、イオウ回収量の減少を伴なわずに、高
がス化効率が・潜られる比較的高温においてガス化処理
を行うことができる5゜本発明の目的から逸脱すること
なく上述の実施列に2いていくつかの/&吏はaT能で
ある。例えば、慾F+はオイル(油)に限られるもので
はなく粒、犬石炭のどと@曲の形状り燃料であってもよ
く、この場合には該−E、科は空気流と共にガス化装置
に導入される。
The l-material from the reaction source is continuously removed through a drain pipe or the like (not shown), and the l-
By replenishing the material, the sulfur retention capacity in the oxidized portion 22 is maintained. The amount of particulate material required will vary depending on the amount of sulfur to be removed from the gas. , this no amount of material! - by varying the amount of particulate material introduced into II and the t of reactive source material removed from the bed.
f) As a result, the presence of calcium in the layer material substantially eliminates the presence of sulfur, which naturally causes the formation of sulfur at a much higher rate. On the other hand, due to the presence of the nori knife, the gasification process can be carried out at a relatively high temperature where high sulfur conversion efficiency can be achieved without reducing the amount of sulfur recovered. Without departing from the purpose, some /& members in the above embodiments are aT functions. For example, F+ is not limited to oil, but may also be grains, coal throat and curved fuels, in which case the -E, family is added to the gasifier along with the air flow. be introduced.

一足範囲の修正、変更、代昏は上述の開示り中に言まれ
、めるj#会には、上で説明し次ものの一部Oみが用い
られる場合もある。従って、特許請求の軸回は、広くし
かも本発明り目的&C合攻するように解釈すべきである
。。
Modifications, changes, and substitutions of the scope are mentioned in the above disclosure, and some of the above and the following may be used in the meeting. Therefore, the terms of the patent claims should be interpreted broadly and in a way that meets the objectives & C of the present invention. .

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

I@/図は、本発明Vこ使用されるがス化装置の断面図
、a2図Lri渠/図の線コーツで切曲した断面図でお
る。 符号の説明 IO・・・tfガス化装 置z・・・格子 14・・・前部壁 16・・・後部壁 22・・・ガス化部 24・・・再生部 16・・・空気ダクト 30・・空気分配管装置
Figure I/ is a cross-sectional view of the oxidation equipment used in the present invention, and Figure A2 is a cross-sectional view cut along the line Coats in Figure A2. Description of symbols IO...tf gasifier z...grid 14...front wall 16...rear wall 22...gasification section 24...regeneration section 16...air duct 30...・Air distribution piping device

Claims (1)

【特許請求の範囲】 (ハ カルシウム及び7リカを含む材料の層を構成し、
前記層にイオヮ含M燃料を導入し、前記層に空気を通し
て前記層を流動化し燃料の燃焼を促進し、並びに、前記
燃料の導入と前記空気の流通と金調督して前記燃料をガ
ス化し前記燃料からイオウ含有がスを放出させる工程を
含み、前記材料中のカルシウムの量を選択して該カルシ
ウムカ前記イオウと反応して前記ガスからイオウの大部
分を除去し、また、前記材料中のシリカのIlヲ選択し
てシリカを含まない場合よシも高9謳度で脱硫の減少を
伴なうことなく前記がス化が生じるようにしたことを特
徴とするイオウ含有燃料のガス化方法。 @ 前記材料中のカルシウムの重量が6oqbからbs
%υ間にろることを%徴とする前記第7項記載9方法。 (j 前記材料中のシリカの点輩が27喝からコ乙悌の
間にあることを特徴とする前記第1項記gItD方′法
。 (至)前記材料中のカルシ9ムとシリカの比が重量で6
0から6S対21から26の範囲にあることを4?像と
する前記第7項記載り方法。 (勺 前記材料t−前記層に導入する前に前記材料を球
又はペレット状にかためる工程を含むことを特徴とする
前記第1項記載の方法1 (6)前記層の温度が約/g00’F (7g2℃) 
に維持されることを%倣とする前記第1項記載の方法。 (η 前記層に迫される空気の徽が燃垢及び発熱を抑え
るよう゛な化学徽崗的剖会でるることを特徴とする前記
第1項記載の方法う
[Scope of Claims]
A sulfur-containing M fuel is introduced into the layer, air is passed through the layer to fluidize the layer to promote combustion of the fuel, and the fuel is gasified by introducing the fuel and controlling the air circulation. releasing sulfur-containing gas from the fuel, selecting an amount of calcium in the material to react the calcium with the sulfur to remove a majority of the sulfur from the gas; Gasification of a sulfur-containing fuel, characterized in that the silica is selected to cause sulfurization to occur with a higher degree of performance than when silica is not included and without a reduction in desulfurization. Method. @ The weight of calcium in the material is from 6 ozb to bs
9. The method described in item 7 above, wherein the % sign is melting between %υ. (j) The gItD method described in item 1 above, characterized in that the silica content in the material is between 27 and 27. (To) The ratio of calcium to silica in the material. is 6 in weight
4 to be in the range of 21 to 26 versus 0 to 6S? 7. The method described in item 7 above. (6) The method according to item 1, which includes the step of clumping the material into a sphere or pellet before introducing the material into the layer. (6) The temperature of the layer is approximately /g00' F (7g2℃)
2. The method according to item 1 above, wherein the % imitation is maintained at . (η) The method according to item 1 above, characterized in that the flow of air that presses against the layer is a chemical reaction that suppresses combustion and heat generation.
JP8245183A 1982-05-14 1983-05-11 Gasification of sulfur-containing fuel Pending JPS58207939A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US37835982A 1982-05-14 1982-05-14
US378359 1982-05-14

Publications (1)

Publication Number Publication Date
JPS58207939A true JPS58207939A (en) 1983-12-03

Family

ID=23492827

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8245183A Pending JPS58207939A (en) 1982-05-14 1983-05-11 Gasification of sulfur-containing fuel

Country Status (2)

Country Link
JP (1) JPS58207939A (en)
GB (1) GB2120118A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE455423B (en) * 1987-05-27 1988-07-11 John Munck Af Rosenschold SETTING OF STRAW OR SIMILAR STRAMATERIAL MAKING GENERATOR GAS, AND DEVICE FOR EXTENDING THE SET

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4872202A (en) * 1971-11-12 1973-09-29
JPS50119805A (en) * 1974-03-08 1975-09-19
JPS5195403A (en) * 1975-01-10 1976-08-21
JPS523603A (en) * 1975-05-09 1977-01-12 Maximilianshuette Eisenwerk Method and apparatus for desulfurization in coal gasification
JPS5241606A (en) * 1975-09-30 1977-03-31 Nippon Steel Corp Method for gasification of coal by using molten slug and molten iron
JPS5475492A (en) * 1977-11-12 1979-06-16 Kloeckner Humboldt Deutz Ag Method and apparatus for producing gas chiefly containing co and h2
JPS55164290A (en) * 1979-01-09 1980-12-20 Exxon Research Engineering Co Conversion of liquid and or solid fuel to almost inerttmatterrfree gas

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4154581A (en) * 1978-01-12 1979-05-15 Battelle Development Corporation Two-zone fluid bed combustion or gasification process

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4872202A (en) * 1971-11-12 1973-09-29
JPS50119805A (en) * 1974-03-08 1975-09-19
JPS5195403A (en) * 1975-01-10 1976-08-21
JPS523603A (en) * 1975-05-09 1977-01-12 Maximilianshuette Eisenwerk Method and apparatus for desulfurization in coal gasification
JPS5241606A (en) * 1975-09-30 1977-03-31 Nippon Steel Corp Method for gasification of coal by using molten slug and molten iron
JPS5475492A (en) * 1977-11-12 1979-06-16 Kloeckner Humboldt Deutz Ag Method and apparatus for producing gas chiefly containing co and h2
JPS55164290A (en) * 1979-01-09 1980-12-20 Exxon Research Engineering Co Conversion of liquid and or solid fuel to almost inerttmatterrfree gas

Also Published As

Publication number Publication date
GB8309977D0 (en) 1983-05-18
GB2120118A (en) 1983-11-30

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