JP3526222B2 - Gas conversion melting furnace - Google Patents
Gas conversion melting furnaceInfo
- Publication number
- JP3526222B2 JP3526222B2 JP25974298A JP25974298A JP3526222B2 JP 3526222 B2 JP3526222 B2 JP 3526222B2 JP 25974298 A JP25974298 A JP 25974298A JP 25974298 A JP25974298 A JP 25974298A JP 3526222 B2 JP3526222 B2 JP 3526222B2
- Authority
- JP
- Japan
- Prior art keywords
- gas
- gas conversion
- pyrolysis
- furnace
- melting furnace
- 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 - Fee Related
Links
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
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E50/00—Technologies for the production of fuel of non-fossil origin
- Y02E50/30—Fuel from waste, e.g. synthetic alcohol or diesel
-
- 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
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W30/00—Technologies for solid waste management
- Y02W30/20—Waste processing or separation
Landscapes
- Feeding And Controlling Fuel (AREA)
- Gasification And Melting Of Waste (AREA)
- Processing Of Solid Wastes (AREA)
- Industrial Gases (AREA)
Description
【0001】[0001]
【発明の属する技術分野】本発明は、廃棄物の熱分解生
成物を燃料ガスに変換するガス変換溶融炉の改良に関す
るものである。TECHNICAL FIELD The present invention relates to an improvement in a gas conversion melting furnace for converting a thermal decomposition product of waste into a fuel gas.
【0002】[0002]
【従来の技術】廃棄物を熱分解処理し、その熱分解生成
物(熱分解ガス、熱分解オイル、熱分解残査)をガス変
換溶融炉に投入して酸素付加により高温処理し、灰分は
スラグとして、有機分は燃料ガスとして回収する技術が
知られている。2. Description of the Related Art Waste is pyrolyzed, and its pyrolyzed products (pyrolysis gas, pyrolysis oil, pyrolysis residue) are put into a gas conversion melting furnace and subjected to high temperature treatment by oxygen addition to remove ash. As a slag, a technique of recovering organic matter as fuel gas is known.
【0003】図3は従来のガス変換溶融炉を示すフロー
であり、廃棄物を熱分解炉1により熱分解処理し、ター
ル分を含んだ熱分解ガスは凝縮器2で冷却・洗浄処理さ
れて熱分解ガスと熱分解オイルに分けられる。また熱分
解残査は、粉砕器3で粉砕される。これらはガス変換溶
融炉4のガス変換溶融部5に直接投入される。ガス変換
溶融部5は酸素付加により1400〜2000℃の高温に保たれ
ている。FIG. 3 is a flow chart showing a conventional gas conversion melting furnace, in which waste is pyrolyzed by the pyrolysis furnace 1 and the pyrolysis gas containing tar is cooled and washed by the condenser 2. It is divided into pyrolysis gas and pyrolysis oil. The thermal decomposition residue is crushed by the crusher 3. These are directly charged into the gas conversion melting part 5 of the gas conversion melting furnace 4. The gas conversion melting part 5 is kept at a high temperature of 1400 to 2000 ° C. by adding oxygen.
【0004】ところが従来のガス変換溶融炉では、熱分
解ガス及び熱分解オイルはガスクラッキングを行うこと
によりCO、H2を主成分とする燃料ガスに改質すること
を主目的としてガス変換溶融炉に投入されているのであ
るが、ガスクラッキングに必要な温度は1000〜1300℃で
あるにもかかわらず、1400〜2000℃のガス変換溶融部5
に投入されているため、無駄な熱量が消費され、酸素供
給量が多く、ガス化効率が悪いという問題があった。However, in the conventional gas conversion melting furnace, the main purpose of the pyrolysis gas and pyrolysis oil is to reform the fuel gas containing CO and H 2 as main components by performing gas cracking. Although the temperature required for gas cracking is 1000 to 1300 ° C, the gas conversion melting part 5 at 1400 to 2000 ° C
However, there is a problem in that wasteful heat is consumed, oxygen is supplied in large amounts, and gasification efficiency is poor.
【0005】また、熱分解ガス及び熱分解オイルをガス
変換溶融部5に直接投入しているため、熱分解ガス及び
熱分解オイルの内部に含まれる水素原子が投入した酸素
と反応し、H2O が発生する。このため、回収される燃
料ガス中の水素量が低下してしまうという問題があっ
た。このガス変換溶融部5で起こる主反応は下記の通り
である。Further, since the pyrolysis gas and the pyrolysis oil are directly fed to the gas conversion melting section 5, hydrogen atoms contained in the pyrolysis gas and the pyrolysis oil react with the introduced oxygen to generate H 2 O is generated. Therefore, there is a problem that the amount of hydrogen in the recovered fuel gas is reduced. The main reactions that take place in the gas conversion / melting section 5 are as follows.
【0006】[0006]
【化1】 [Chemical 1]
【0007】[0007]
【発明が解決しようとする課題】本発明は上記した従来
の問題点を解決し、廃棄物の熱分解生成物から、熱量の
無駄を生ずることなくガス化効率及び水素含有率の高い
燃料ガスを効率良く得ることができるガス変換溶融炉を
提供するためになされたものである。DISCLOSURE OF THE INVENTION The present invention solves the above-mentioned problems of the prior art, and produces a fuel gas having a high gasification efficiency and a high hydrogen content rate from the thermal decomposition products of wastes without wasting heat. This is done to provide a gas conversion melting furnace that can be efficiently obtained.
【0008】[0008]
【課題を解決するための手段】上記の課題を解決するた
めになされた本発明のガス変換溶融炉は、廃棄物の熱分
解炉に接続され、熱分解生成物を燃料ガスに変換するガ
ス変換溶融炉の炉体の5〜30気圧に保持した内部を、
1400℃〜2000℃のガス変換溶融部と、その下方
に位置する、1000℃〜1300℃のガスクラッキン
グ部とに区画し、前記熱分解生成物のうち熱分解残査は
ガス変換溶融部に投入し、熱分解ガスおよび熱分解オイ
ルは分離することなくガスクラッキング部に投入するよ
うにしたガス変換溶融炉であって、前記熱分解炉を前記
ガス変換溶融炉よりも高圧下で廃棄物を熱分解するよう
にしたことを特徴とするものである。なお、このガスク
ラッキング部に、流量制御可能な酸素及びメタンの供給
ラインを設けることが好ましい。The gas conversion melting furnace of the present invention made to solve the above problems is connected to a waste thermal decomposition furnace to convert the thermal decomposition products into fuel gas. The inside of the furnace body of the melting furnace maintained at 5-30 atm ,
Gas conversion melting part at 1400 ° C- 2000 ° C and below
Located at 1000 ° C. to 1300 ° C., and the pyrolysis residue of the pyrolysis products is introduced into the gas conversion melting section, and the pyrolysis gas and pyrolysis oil are not separated. A gas conversion melting furnace adapted to be introduced into a gas cracking section , wherein the pyrolysis furnace is
Pyrolysis of waste under higher pressure than gas conversion melting furnace
It is characterized by having done. Incidentally, the gas cracking unit of this, it is preferable to provide a supply line of the flow rate controllable oxygen and methane.
【0009】[0009]
【発明の実施の形態】以下に本発明を、好ましい実施形
態とともに更に詳細に説明する。図1は本発明の第1の
実施形態を示すもので、5〜30気圧の高圧に保たれた
ガス変換溶融炉の炉体10の内部を、ガス変換溶融部1
1とその下方に位置するガスクラッキング部12と急冷
部19とに区画してある。ガス変換溶融部11は従来と
同様に1400〜2000℃の高温であるが、これの下
方に隣接して設けられたガスクラッキング部12は、1
000〜1300℃に温度設定されている。ガス変換溶
融部11には酸素供給ライン13から酸素が投入されて
いる。またガスクラッキング部12は低酸素濃度に維持
されている。ガスクラッキング部12には、流量制御可
能な酸素供給ライン14とメタン供給ライン15とを設
けることが好ましい。BEST MODE FOR CARRYING OUT THE INVENTION The present invention will be described in more detail below together with preferred embodiments. FIG. 1 shows a first embodiment of the present invention, in which the inside of a furnace body 10 of a gas conversion melting furnace kept at a high pressure of 5 to 30 atm is provided with a gas conversion melting part 1
1 and a gas cracking section 12 and a quenching section 19 located below it . The gas conversion melting portion 11 is a high temperature as in the prior art to 1400 to 2000 ° C., under which
The gas cracking part 12 provided adjacent to
The temperature is set to 000 to 1300 ° C. Oxygen is supplied to the gas conversion / melting section 11 from the oxygen supply line 13. Further, the gas cracking portion 12 is maintained at a low oxygen concentration. The gas cracking section 12 is preferably provided with an oxygen supply line 14 and a methane supply line 15 whose flow rates can be controlled.
【0010】16はガス変換溶融炉の前段に設置される
廃棄物の熱分解炉であり、550 ℃程度の温度で廃棄物を
熱分解し、熱分解オイルを含む熱分解炉ガスと熱分解残
査(チャー)とする。熱分解残査は、粉砕器17で粉砕
したうえでガス変換溶融部11に投入され、前記の1、
2式により主にCOガスに変換されて回収される。一
方、熱分解オイルを含む熱分解炉ガスは凝縮器18で熱
分解オイルと熱分解炉ガスとに分離され、ともにガスク
ラッキング部12に投入される。このように熱分解オイ
ルと熱分解炉ガスとに分離するのは、5〜30気圧の高
圧に保たれたガス変換溶融炉の炉体10の内部に、気体
・液体それぞれに専用のポンプを用いてこれらを円滑に
圧送するためである。1300℃以下で低酸素濃度のガスク
ラッキング部12で起こるクラッキング反応は下記の7
式の通りであり、急冷部19からCO、H2を主成分とす
る燃料ガスを回収することができる。Reference numeral 16 denotes a waste thermal decomposition furnace installed in the preceding stage of the gas conversion melting furnace, which thermally decomposes the waste at a temperature of about 550 ° C., and the thermal decomposition gas containing thermal decomposition oil and the thermal decomposition residue. It is a char. The thermal decomposition residue is pulverized by a pulverizer 17 and then introduced into the gas conversion / melting section 11, where the above-mentioned 1,
It is mainly converted into CO gas and recovered by the two equations. On the other hand, the pyrolysis furnace gas containing pyrolysis oil heat in the condenser 18
It is separated into cracked oil and pyrolysis furnace gas, and both are put into the gas cracking section 12. Thus pyrolysis oy
In order to separate the gas and the pyrolysis furnace gas into the furnace body 10 of the gas conversion and melting furnace kept at a high pressure of 5 to 30 atm, these are smoothly pumped using dedicated pumps for gas and liquid respectively. This is to send by pressure. 1300 ° C. in a low oxygen concentration below the cracking reactions occurring in the gas cracking unit 12 below 7
According to the formula, the fuel gas containing CO and H 2 as main components can be recovered from the quenching section 19.
【0011】本発明のガス変換溶融炉によれば、熱分解
オイルと熱分解ガスとをガス変換溶融部11より低温の
ガスクラッキング部12へ投入するため、以下の理由で
熱量を低減することができる。1)
熱分解オイルと熱分解ガスを反応温度まで上げる
顕熱量を軽減することができる。2)
ガスクラッキング部12では、ガス変換溶融部1
1からの1400℃以上の高温ガスの顕熱を反応に利用でき
る。必要熱量の軽減により、供給酸素量を削減できるた
め、生成する燃料ガスのガス化効率は高くなる。According to the gas conversion melting furnace of the present invention, the pyrolysis oil and the pyrolysis gas are introduced into the gas cracking section 12 at a temperature lower than that of the gas conversion melting section 11, so that the heat quantity can be reduced for the following reasons. it can. 1) The amount of sensible heat that raises the pyrolysis oil and the pyrolysis gas to the reaction temperature can be reduced. 2) In the gas cracking section 12, the gas conversion melting section 1
The sensible heat of hot gas from 1 to 1400 ℃ or higher can be used for the reaction. Since the amount of oxygen supplied can be reduced by reducing the required heat amount, the gasification efficiency of the produced fuel gas is increased.
【0012】[0012]
【化2】 [Chemical 2]
【0013】この7式と6式とがガスクラッキング部1
2での主反応となる。6式の平衡反応は高温ほど右側に
移動する反応である。本発明のガス変換溶融炉では、ガ
ス変換溶融部11には熱分解残査が投入されるのみであ
るからガス変換溶融部11での前記3式の反応が少なく
なり、逆にガスクラッキング部12での7式の反応が起
こるため、水素発生量は増加する。また、ガスクラッキ
ング部12はガス変換溶融部11に比べて低温のために
平衡はより左側に進行し、水素発生量が増加する。These equations 7 and 6 are the gas cracking section 1
It becomes the main reaction in 2. The equilibrium reaction of equation 6 is a reaction that moves to the right as the temperature rises. In the gas conversion / melting furnace of the present invention, only the thermal decomposition residue is put into the gas conversion / melting section 11, so that the reactions of the above three equations in the gas conversion / melting section 11 are reduced, and conversely, the gas cracking section 12 The hydrogen generation amount increases because the reaction of the equation ( 7) occurs. In addition, the gas cracking section 12 has a lower temperature than the gas conversion and melting section 11, so that the equilibrium advances to the left and the hydrogen generation amount increases.
【0014】このように、本発明のガス変換溶融炉で
は、熱分解オイルと熱分解炉ガスとをガス変換溶融部1
1より低温のガスクラッキング部12に投入するため、
1400℃以上のガス変換溶融部に投入していた従来に比較
して熱量消費を軽減し、酸素供給量を削減できるため、
回収燃料ガスのガス化効率を高くすることができる。ま
た本発明のガス変換溶融炉によれば回収される燃料ガス
中の水素量を増加させることができる。As described above, in the gas conversion melting furnace of the present invention, the pyrolysis oil and the pyrolysis furnace gas are mixed in the gas conversion melting section 1
In order to put it in the gas cracking section 12 at a temperature lower than 1,
Compared with the conventional method in which the gas conversion and melting section at 1400 ° C or higher is used, the heat consumption can be reduced and the oxygen supply can be reduced,
The gasification efficiency of the recovered fuel gas can be increased. Further, according to the gas conversion melting furnace of the present invention, the amount of hydrogen in the recovered fuel gas can be increased.
【0015】なお、水素はメタンに比べて付加価値が高
いため、メタン供給ライン15からメタンを補助剤とし
てガスクラッキング部12に投入し、水素の発生量を増
加させることができる。また必要に応じて酸素供給ライ
ン14から酸素をガスクラッキング部12に投入し、燃
料ガスの性状を制御することができる。Since hydrogen has a higher added value than methane, methane can be fed from the methane supply line 15 to the gas cracking section 12 as an auxiliary agent to increase the amount of hydrogen generated. If necessary, oxygen can be introduced into the gas cracking unit 12 from the oxygen supply line 14 to control the properties of the fuel gas.
【0016】図2は本発明の第2の実施形態を示すもの
である。この実施形態では、ガス変換溶融炉の前段に高
圧熱分解炉20が設置され、廃棄物をガス変換溶融炉よ
りも更に高圧下で廃棄物を熱分解する。この実施形態で
は、熱分解炉ガスを熱分解オイルと分離することなく圧
力差を利用してガス変換溶融炉のガスクラッキング部1
2に投入することができる。このため、第1の実施形態
のように凝縮器18で熱分解オイルを分離する必要がな
く、消費熱量を更に削減することができる。また、第1
の実施形態においては凝縮器18で失われていた水溶性
の高分子有機物が、第2の実施形態ではガスクラッキン
グ部12に入ることにより、燃料ガスの回収量を増加さ
せることができる。FIG. 2 shows a second embodiment of the present invention. In this embodiment, the high-pressure pyrolysis furnace 20 is installed in the preceding stage of the gas conversion melting furnace, and the waste is pyrolyzed under a higher pressure than that of the gas conversion melting furnace. In this embodiment, the gas cracking unit 1 of the gas conversion melting furnace is utilized by utilizing the pressure difference without separating the pyrolysis furnace gas from the pyrolysis oil.
2 can be thrown in. Therefore, it is not necessary to separate the pyrolysis oil in the condenser 18 as in the first embodiment, and the heat consumption can be further reduced. Also, the first
In the second embodiment, the water-soluble polymer organic matter lost in the condenser 18 enters the gas cracking section 12 in the second embodiment, so that the recovery amount of the fuel gas can be increased.
【0017】次に、本発明の効果を確認するための計算
例を示す。計算は、図1に示した本発明のガス変換溶融
炉と、図3に示した従来のガス変換溶融炉について行っ
た。計算の前提として、ガス変換溶融の温度はともに16
00℃(本発明ではガスクラッキング部は1200℃)とし、
ともに熱分解ガスの供給量は300Nm3、熱分解オイルの
供給量は1200kg、熱分解チャーの供給量は1000kgとし
た。その結果は次の通りである。Next, a calculation example for confirming the effect of the present invention will be shown. The calculation was performed for the gas conversion melting furnace of the present invention shown in FIG. 1 and the conventional gas conversion melting furnace shown in FIG. As a premise of the calculation, the gas conversion melting temperature is 16
00 ° C (in the present invention, the gas cracking part is 1200 ° C),
In both cases, the amount of pyrolysis gas supplied was 300 Nm 3 , the amount of pyrolysis oil supplied was 1200 kg, and the amount of pyrolysis char supplied was 1000 kg. The results are as follows.
【0018】[0018]
【表1】 [Table 1]
【0019】[0019]
【発明の効果】以上に説明したように、本発明によれば
ガス変換プロセスの消費熱量を削減することにより、ガ
ス化効率を高めることができる。また、回収燃料ガス中
の水素量を増加させることができる。さらに請求項2に
記載のように、前段に高圧熱分解炉を用いれば、水溶性
の高分子有機物がガスクラッキング部に入ることによ
り、燃料ガスの回収量を増加させることができ、ガス変
換プロセスの消費熱量を一段と削減することができる。As described above, according to the present invention, the gasification efficiency can be improved by reducing the heat consumption of the gas conversion process. In addition, the amount of hydrogen in the recovered fuel gas can be increased. Further, as described in claim 2, if a high-pressure pyrolysis furnace is used in the preceding stage, the water-soluble polymer organic matter enters the gas cracking section, so that the recovery amount of the fuel gas can be increased and the gas conversion process. It is possible to further reduce the heat consumption of.
【図1】請求項1の発明の実施形態を示すフローチャー
トである。FIG. 1 is a flowchart showing an embodiment of the invention of claim 1.
【図2】請求項2の発明の実施形態を示すフローチャー
トである。FIG. 2 is a flow chart showing an embodiment of the invention of claim 2;
【図3】従来例を示すフローチャートである。FIG. 3 is a flowchart showing a conventional example.
1 熱分解炉、2 凝縮器、3 粉砕器、4 従来のガ
ス変換溶融炉、5 ガス変換溶融部、10 本発明のガ
ス変換溶融炉の炉体、11 ガス変換溶融部、12 ガ
スクラッキング部、13 ガス変換溶融部への酸素供給
ライン、14 ガスクラッキング部への酸素供給ライ
ン、15 メタン供給ライン、16 廃棄物の熱分解
炉、17 粉砕器、18凝縮器、19 急冷部、20
高圧熱分解炉1 Pyrolysis furnace, 2 Condenser, 3 Crusher, 4 Conventional gas conversion melting furnace, 5 Gas conversion melting section, 10 Gas conversion melting furnace furnace body of the present invention, 11 Gas conversion melting section, 12 Gas cracking section, 13 Oxygen supply line to gas conversion / melting section, 14 Oxygen supply line to gas cracking section, 15 Methane supply line, 16 Waste thermal decomposition furnace, 17 Crusher, 18 Condenser, 19 Quenching section, 20
High pressure pyrolysis furnace
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI F23G 5/14 B09B 3/00 ZAB F23K 5/00 303 303K (56)参考文献 特開2000−70894(JP,A) 特開 昭55−51475(JP,A) 特開 平11−294726(JP,A) 特開 平11−290810(JP,A) 特開 平11−281022(JP,A) 特開 平11−270823(JP,A) 特開 平11−216445(JP,A) 特開 平11−193913(JP,A) 特開 平11−173523(JP,A) 特開 平11−169818(JP,A) 特開 平11−159721(JP,A) 特開 平10−339416(JP,A) 特開 平10−337555(JP,A) 特開 平10−310783(JP,A) 特開 平10−205723(JP,A) 特開 平10−156314(JP,A) 特開 平10−132237(JP,A) 特開 平10−130662(JP,A) 特開 平10−128288(JP,A) 特開 平10−81885(JP,A) 特開 平9−229324(JP,A) 特開 平5−126327(JP,A) (58)調査した分野(Int.Cl.7,DB名) F23G 5/00 - 5/50 F23K 5/00 - 5/22 B09B 3/00 C10K 3/00 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 7 Identification code FI F23G 5/14 B09B 3/00 ZAB F23K 5/00 303 303K (56) Reference JP 2000-70894 (JP, A) JP JP-A-55-51475 (JP, A) JP-A-11-294726 (JP, A) JP-A-11-290810 (JP, A) JP-A-11-281022 (JP, A) JP-A-11-270823 (JP , A) JP 11-216445 (JP, A) JP 11-193913 (JP, A) JP 11-173523 (JP, A) JP 11-169818 (JP, A) JP 11-159721 (JP, A) JP 10-339416 (JP, A) JP 10-337555 (JP, A) JP 10-310783 (JP, A) JP 10-205723 (JP, A) JP-A-10-156314 (JP, A) JP-A-10-132237 (JP, A) JP-A-10-130662 (JP , A) JP-A-10-128288 (JP, A) JP-A-10-81885 (JP, A) JP-A-9-229324 (JP, A) JP-A-5-126327 (JP, A) (58) Fields investigated (Int.Cl. 7 , DB name) F23G 5/00-5/50 F23K 5/00-5/22 B09B 3/00 C10K 3/00
Claims (2)
成物を燃料ガスに変換するガス変換溶融炉の炉体の5〜
30気圧に保持した内部を、1400℃〜2000℃の
ガス変換溶融部と、その下方に位置する、1000℃〜
1300℃のガスクラッキング部とに区画し、前記熱分
解生成物のうち熱分解残査はガス変換溶融部に投入し、
熱分解ガスおよび熱分解オイルは分離することなくガス
クラッキング部に投入するようにしたガス変換溶融炉で
あって、前記熱分解炉を前記ガス変換溶融炉よりも高圧
下で廃棄物を熱分解するようにしたことを特徴とするガ
ス変換溶融炉。1. A connected to the pyrolysis furnace waste, 5 gas conversion melting furnace of the furnace body for converting heat decomposition products into the fuel gas
The inside kept at 30 atm was 1400 ° C. to 2000 ° C., and the gas conversion and melting part was located below it.
It is divided into a gas cracking section at 1300 ° C., and the thermal decomposition residue of the thermal decomposition products is introduced into the gas conversion melting section,
In the gas conversion melting furnace, the pyrolysis gas and pyrolysis oil are put into the gas cracking section without separation.
There is a higher pressure in the pyrolysis furnace than in the gas conversion melting furnace.
A gas conversion melting furnace characterized in that waste is pyrolyzed below .
酸素及びメタンの供給ラインを設けた請求項1に記載の
ガス変換溶融炉。 2. The gas conversion melting furnace according to claim 1, wherein the gas cracking section is provided with oxygen and methane supply lines whose flow rates can be controlled.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP25974298A JP3526222B2 (en) | 1998-09-14 | 1998-09-14 | Gas conversion melting furnace |
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| Application Number | Priority Date | Filing Date | Title |
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| JP25974298A JP3526222B2 (en) | 1998-09-14 | 1998-09-14 | Gas conversion melting furnace |
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| JP2000087050A JP2000087050A (en) | 2000-03-28 |
| JP3526222B2 true JP3526222B2 (en) | 2004-05-10 |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| FR2859216B1 (en) * | 2003-08-27 | 2008-07-04 | Inst Francais Du Petrole | METHOD AND PLANT FOR HIGH-YIELD PRODUCTION OF A SYNTHESIS GAS DEPOLLUED FROM A CHARGE RICH IN ORGANIC MATERIAL |
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