JPS606786A - Reactor for carbon - Google Patents
Reactor for carbonInfo
- Publication number
- JPS606786A JPS606786A JP11468283A JP11468283A JPS606786A JP S606786 A JPS606786 A JP S606786A JP 11468283 A JP11468283 A JP 11468283A JP 11468283 A JP11468283 A JP 11468283A JP S606786 A JPS606786 A JP S606786A
- Authority
- JP
- Japan
- Prior art keywords
- carbon
- zone
- combustion
- gasification
- reactor
- 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
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 title claims abstract description 46
- 229910052799 carbon Inorganic materials 0.000 title claims abstract description 46
- 238000002485 combustion reaction Methods 0.000 claims abstract description 35
- 239000002245 particle Substances 0.000 claims abstract description 30
- 238000002309 gasification Methods 0.000 claims abstract description 26
- 238000006243 chemical reaction Methods 0.000 claims abstract description 7
- 239000007789 gas Substances 0.000 abstract description 25
- 239000001257 hydrogen Substances 0.000 abstract description 16
- 229910052739 hydrogen Inorganic materials 0.000 abstract description 16
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 12
- 239000012530 fluid Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 description 7
- 238000005984 hydrogenation reaction Methods 0.000 description 5
- 239000000567 combustion gas Substances 0.000 description 3
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 238000003763 carbonization Methods 0.000 description 2
- 239000003245 coal Substances 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000012495 reaction gas Substances 0.000 description 2
- 239000012429 reaction media Substances 0.000 description 2
- 235000019738 Limestone Nutrition 0.000 description 1
- 241000219094 Vitaceae Species 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 235000021021 grapes Nutrition 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
Landscapes
- Carbon And Carbon Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
〔発明の利用分野〕
本発明は、カーボンを含む粒子を水性ガス化して高濃度
の水素會得るカーボンの反応装置に係り、特に未反応の
カーボンを低減しつつ高濃度の水素を得るのに好適なカ
ーボンの反応装置に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Field of Application of the Invention] The present invention relates to a carbon reaction device capable of producing a high concentration of hydrogen by converting carbon-containing particles into water gas. The invention relates to a carbon reactor suitable for obtaining hydrogen.
−〔発明の背景〕
石炭をガス化して最終的に代替天然ガスを得る高カロリ
ーガス化プロセスの開発が近年、盛んに進められている
。このプロセスを大別すると乾留炉、水添炉および水性
炉の3つの要素で構成でれている。このプロセスにおい
ては、最初に石炭は乾留炉で乾留てれてチャー?生成し
、このチャーは水添炉に導かれ水性炉からの水素リッチ
ガスで水添反応する。この水素リツチガスは水添炉で生
じた未反応チャーを水性炉で水性ガス化することにより
得られる。したがって水性炉出口の水素濃度はできるだ
け高い方が望ましく、このため従来水性炉での水素製造
方法に関し種々の検討がな嘔れている。- [Background of the Invention] In recent years, the development of high-calorie gasification processes for gasifying coal and ultimately obtaining alternative natural gas has been actively promoted. Broadly speaking, this process consists of three elements: a carbonization furnace, a hydrogenation furnace, and an aqueous furnace. In this process, coal is first carbonized in a carbonization furnace to form a char. This char is then led to a hydrogenation furnace and undergoes a hydrogenation reaction with hydrogen-rich gas from the water-based furnace. This hydrogen-rich gas is obtained by converting unreacted char produced in a hydrogenation furnace into water gas in a water-based furnace. Therefore, it is desirable that the hydrogen concentration at the outlet of a water-based reactor be as high as possible, and for this reason, various studies have been made regarding methods for producing hydrogen in a water-based reactor.
このような水性炉での水床製造方法の最も一般的な方法
は、水性炉で水性反応と部分酸化あるいは燃焼反応を同
時に行なわせて生成したガス全そのまま水添炉に供給す
る方法である。しかしこの方法では生成ガス中に副生じ
たC02ガスが含1れるので生成ガス中の水素濃度が低
下する欠点がある。また生成ガス中の水素濃度を高める
ため、酸化鉄や石灰石等の反応媒体を用いて副生するC
OやCOt k分離するプロセスが検討逼れている。こ
のプロセスでは生成ガス中の水素濃度全高めることは可
能であるが1反応媒体の活性劣化及び粉化によるトラブ
ルが生じ、実用化が困難である。The most common method for producing a water bed in such a water-based reactor is to simultaneously carry out an aqueous reaction and a partial oxidation or combustion reaction in the water-based reactor, and supply all of the gas produced as it is to the hydrogenation reactor. However, this method has the disadvantage that the hydrogen concentration in the produced gas decreases because the produced gas contains CO2 gas produced as a by-product. In addition, in order to increase the hydrogen concentration in the generated gas, a reaction medium such as iron oxide or limestone is used to generate carbon by-product.
The process of separating O and COt is under consideration. In this process, it is possible to increase the total hydrogen concentration in the produced gas, but problems arise due to deterioration of the activity of one reaction medium and powdering, making it difficult to put it into practical use.
一方、生成ガス中の水素濃度を高めるため、層内カーボ
ン濃度を上げると未反応カーボンの量が多くなり、ガス
化炉の効率が低下する。このため。On the other hand, if the intralayer carbon concentration is increased in order to increase the hydrogen concentration in the generated gas, the amount of unreacted carbon will increase and the efficiency of the gasifier will decrease. For this reason.
ガス化炉の効率が高く、かつ生成ガス中の水素濃度を高
くすることができるカーボンの反応装置が要望嘔れてい
た。There has been a demand for a carbon reactor that has a high gasifier efficiency and can increase the hydrogen concentration in the produced gas.
本発明の目的は、未反応カーボンの量を減少させてガス
化炉の効率全高めながら水素濃度の高い水性ガスを得る
ことができるカーボンの反応装置會提供することにある
。SUMMARY OF THE INVENTION An object of the present invention is to provide a carbon reactor that can reduce the amount of unreacted carbon and increase the efficiency of the gasifier while producing aqueous gas with a high hydrogen concentration.
本発明は、ガス化炉で生成する燃焼ガスと水性反応ガス
と葡それぞれ分離して取り出すため、ガス化炉内をカー
ボンの燃焼ゾーンとガス化ゾーンとに区画し、これらの
ゾーン間にカーボン粒子奮循環芒ぜることによってカー
ボン粒子の熱全有効に利用し、また各ゾーン間のカーボ
ン粒子循環域全流動層域として燃焼ガスと水性反応ガス
との混入全防止し、嘔らにガス化炉の下部において未反
応カーボン全燃焼して未反応カーボン全減少嘔せるよう
にしたものである。The present invention divides the inside of the gasifier into a carbon combustion zone and a gasification zone, and separates carbon particles between these zones in order to separate and take out the combustion gas, water-based reaction gas, and grapes generated in the gasifier. By actively circulating the carbon particles, all the heat of the carbon particles can be used effectively, and the entire carbon particle circulation area between each zone is a fluidized bed area, which completely prevents the mixture of combustion gas and aqueous reaction gas, and is useful for the gasification furnace. The unreacted carbon is completely combusted in the lower part of the tank to reduce the total amount of unreacted carbon.
本発明の実施例全第1図に示す。第1図において1円筒
状のガス化炉本体1の内部には炉と同心円上に内筒2お
よび外筒3が設けられている。内筒2の内部側は燃焼ゾ
ーン4.内筒2の外側はガス化ゾーン5奮それぞれ構成
し、内筒2と外筒3との間隙部分はカーボン粒子の溢流
部6となっている。ガス化炉本体lの略中央部よりも下
方側は縮径され、その炉側壁と内筒2との間隙部分は移
動層部8となっている。内筒2の下方には炉側壁に沿っ
て断面台形状の突起部が設けられ、Cの突起部によって
絞り部9が形成づれ、この絞り部9の下方の炉内部がカ
ーボン燃焼炉10となっている。An entire embodiment of the invention is shown in FIG. In FIG. 1, inside a cylindrical gasifier body 1, an inner cylinder 2 and an outer cylinder 3 are provided concentrically with the furnace. The inner side of the inner cylinder 2 is a combustion zone 4. The outer side of the inner cylinder 2 constitutes a gasification zone 5, and the gap between the inner cylinder 2 and the outer cylinder 3 forms an overflow part 6 of carbon particles. The diameter of the gasifier main body l is reduced below the substantially central portion, and the gap between the furnace side wall and the inner cylinder 2 forms a moving bed portion 8. A protrusion with a trapezoidal cross section is provided below the inner cylinder 2 along the furnace side wall, and the protrusion C forms a constriction part 9, and the inside of the furnace below the constriction part 9 becomes a carbon combustion furnace 10. ing.
このよう彦ガス化炉においてカーボン粒子む粒子は1反
応器本体1の燃焼ゾーン4で燃焼し嘔らに粒子紮循環し
てガス化ゾーン5でガス化する。In such a Hiko gasifier, particles including carbon particles are burned in the combustion zone 4 of one reactor main body 1, circulated through the particles, and gasified in the gasification zone 5.
燃焼ゾーン4では燃焼に必要な望気をカーボン燃焼炉1
0の空気供給口11より供給し、カーボン粒子を燃焼嘔
せる。燃焼により高温となった粒子の大部分は、燃焼ゾ
ーン4より粒子循環部である溢流部6會通ってガス化ゾ
ーン5に入る。−万高温の燃焼ガスは、燃焼ゾーン4で
粒子との熱交換を終えた後、ガス分離板としての外筒3
の内部を通って燃焼ゾーン出口管12より糸外に排気さ
れる。ガス化ゾーン4に入った粒子はスチーム供給口1
3より分散板14會経て供給嘔れるスチームにより流動
ガス化し、ガス化ゾーン出口管15より糸外に生成ガス
が抜き出される。水性ガス化ゾーン5で反応した粒子F
i1層下層上部移動層部8全通って燃焼ゾーン4へ再び
入る。なお、ガス化に必要なカーボンはカーボン粒子供
給口16から補給嘔れる。In combustion zone 4, the desired air necessary for combustion is transferred to carbon combustion furnace 1.
The air is supplied from the air supply port 11 of 0, and the carbon particles are combusted. Most of the particles heated to high temperature by combustion enter the gasification zone 5 from the combustion zone 4 through an overflow section 6 which is a particle circulation section. -After the high-temperature combustion gas has finished heat exchange with the particles in the combustion zone 4, the outer cylinder 3 as a gas separation plate
It passes through the inside of the combustion zone and is exhausted to the outside through the combustion zone outlet pipe 12. Particles entering gasification zone 4 are transferred to steam supply port 1
3 through the distribution plate 14, the generated gas is fluidized and gasified, and the generated gas is extracted from the gasification zone outlet pipe 15 to the outside of the yarn. Particles F reacted in water gasification zone 5
It passes through the entire lower upper moving layer section 8 of the i1 layer and enters the combustion zone 4 again. Note that carbon necessary for gasification is supplied from the carbon particle supply port 16.
この際燃焼ゾーン4の未反応酸素が溢流部6を流れる粒
子とともにガス化ゾーン5に混入すると爆発する危険が
あるため、溢流部6に粒子の移動層を形成してガス流れ
に抵抗をもたせ、ガスの混入を減少する。また、ガス化
ゾーン下部の移動層部8においても燃焼ゾーン、4へ供
給した空気が移動層部8よりガス化ゾーン5へ混入しな
いように粒子の移動層を形成し、このガス混入全防止す
る。At this time, there is a risk of explosion if unreacted oxygen in the combustion zone 4 mixes with particles flowing through the overflow section 6 into the gasification zone 5, so a moving layer of particles is formed in the overflow section 6 to resist the gas flow. to reduce gas contamination. Furthermore, in the moving bed section 8 at the lower part of the gasification zone, a moving layer of particles is formed so that the air supplied to the combustion zone 4 does not mix into the gasification zone 5 from the moving bed section 8, and this gas mixing is completely prevented. .
したがって燃焼ゾーンとガス化ゾーンの粒子循環部に移
動層音形成することにより1粒子を循環しながら両反応
ゾーン間のガス混入を非常に小さくできる。Therefore, by forming a moving bed sound in the particle circulation sections of the combustion zone and the gasification zone, gas contamination between both reaction zones can be minimized while circulating one particle.
また層内カーボ/の量會多くして生成ガス中の水素濃度
全高<L7を場合、移動層部8を流下するカーボン粒子
中、未反応カーボンが多くなる。しかし、この未反応カ
ーボンは絞り部9よりカーボン燃焼炉JO内に入り、そ
こで燃焼芒れて生じる燃焼熱がガス化効率に寄与するこ
とになる。したがってカーボンロスゲ非常に小テ<シつ
つ、ガス化効率を上げることができる。カーボンの燃焼
によって生じた灰は灰排出口17より系外に排出芒れる
。Further, if the amount of carbon in the layer is increased so that the total hydrogen concentration in the generated gas is less than L7, unreacted carbon will increase in the carbon particles flowing down the moving bed section 8. However, this unreacted carbon enters the carbon combustion furnace JO through the throttle section 9, where it is combusted and the combustion heat generated contributes to the gasification efficiency. Therefore, the gasification efficiency can be increased while using a very small amount of carbon loss gel. Ash generated by combustion of carbon is discharged outside the system through an ash discharge port 17.
以上のように本発明によれば、水性反応と燃焼反応とを
ひとつのガス化炉内で分離して行い、それぞれの反応に
よって生じたガス會互いに混入しないようにして別個に
抜き出すことができるので水素濃度の高いガスケ得るこ
とができる。また層内カーボンの量全多くして更に水素
濃度の高いガス全得る場合にもカーボンロスと・少なく
することができる。As described above, according to the present invention, the aqueous reaction and the combustion reaction can be carried out separately in one gasifier, and the gases produced by each reaction can be extracted separately without mixing with each other. Gasket with high hydrogen concentration can be obtained. Furthermore, carbon loss can be reduced even when the total amount of carbon in the layer is increased to obtain a gas with a higher hydrogen concentration.
第1図は本発明の一実施例を示す概略的構成図である。 2・・・内筒、 3・・・外筒。 4゛゛燃焼ゾーン、 5由ガス化ゾーン。 6゛°゛°゛溢流動層)、8・・・移動層部。 9・絞り部、 10・・・カーボン燃焼炉。 代理人 鵜 沼 辰 之 第1 2− し 6・。 5、);1ノ →〜15 コ 4 FIG. 1 is a schematic configuration diagram showing an embodiment of the present invention. 2...Inner cylinder, 3...Outer cylinder. 4. Combustion zone, 5. Gasification zone. 6゛°゛°゛overflowing fluidized bed), 8...moving bed section. 9. Throttle part, 10... Carbon combustion furnace. Agent Tatsuyuki Unuma 1st 2- death 6. 5,);1no →~15 Ko 4
Claims (1)
でれ、これらのゾーン間にカーボン粒子を循環嘔せる反
応炉を備えたカーボンの反応装置において、前記燃焼ゾ
ーンと前記ガス化ゾーンとの間のカーボン粒子循環区域
全流動層域とすると七もに前記反応炉の下部に反応炉内
の未反応カーボン會燃焼嘔せるための燃焼炉1f設けた
こと?]l−特徴とするカーボンの反応装置。 (2、特許請求の範囲第1項において、前記燃焼ゾーン
とガス化ゾーンとは反応炉内にこの炉と同心円上に設け
られた筒体により区画芒れて(八ることを特徴とするカ
ーボンの反応装置。 (3)特許請求の範囲第1項において、前記筒体の下方
に絞り部が設けられ、この絞り部の下方に燃焼炉が設け
られていることを特徴とするカーボンの反応装置。[Scope of Claims] (1) In a carbon reactor equipped with a reactor which is divided into a carbon combustion zone and a carbon gasification zone and circulates carbon particles between these zones, If the carbon particle circulation area between the gasification zone and the entire fluidized bed area is assumed, a combustion furnace 1f is provided at the bottom of the reactor to burn off the unreacted carbon in the reactor. ] l-Characterized carbon reactor. (2. In claim 1, the combustion zone and the gasification zone are partitioned by a cylindrical body provided in a reactor concentrically with the reactor. (3) The carbon reaction device according to claim 1, characterized in that a constriction section is provided below the cylindrical body, and a combustion furnace is provided below the constriction section. .
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11468283A JPS606786A (en) | 1983-06-24 | 1983-06-24 | Reactor for carbon |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11468283A JPS606786A (en) | 1983-06-24 | 1983-06-24 | Reactor for carbon |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS606786A true JPS606786A (en) | 1985-01-14 |
Family
ID=14643999
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11468283A Pending JPS606786A (en) | 1983-06-24 | 1983-06-24 | Reactor for carbon |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS606786A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1999031202A1 (en) * | 1997-12-18 | 1999-06-24 | Ebara Corporation | Fuel gasifying system |
-
1983
- 1983-06-24 JP JP11468283A patent/JPS606786A/en active Pending
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1999031202A1 (en) * | 1997-12-18 | 1999-06-24 | Ebara Corporation | Fuel gasifying system |
| US6949224B1 (en) | 1997-12-18 | 2005-09-27 | Ebara Corporation | Fuel gasification system |
| US7390337B2 (en) | 1997-12-18 | 2008-06-24 | Ebara Corporation | Fuel gasification system |
| US7618469B2 (en) | 1997-12-18 | 2009-11-17 | Ebara Corporation | Fuel gasification system |
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