JPH0374493A - Carbon monoxide modifying method in town gas-producing plant and equipment therefor - Google Patents
Carbon monoxide modifying method in town gas-producing plant and equipment thereforInfo
- Publication number
- JPH0374493A JPH0374493A JP1209709A JP20970989A JPH0374493A JP H0374493 A JPH0374493 A JP H0374493A JP 1209709 A JP1209709 A JP 1209709A JP 20970989 A JP20970989 A JP 20970989A JP H0374493 A JPH0374493 A JP H0374493A
- Authority
- JP
- Japan
- Prior art keywords
- city gas
- carbon monoxide
- temperature
- town gas
- reaction
- 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.)
- Granted
Links
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 title claims description 23
- 229910002091 carbon monoxide Inorganic materials 0.000 title claims description 22
- 238000000034 method Methods 0.000 title claims description 15
- 238000006243 chemical reaction Methods 0.000 claims abstract description 47
- 239000003054 catalyst Substances 0.000 claims abstract description 43
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 31
- 238000004519 manufacturing process Methods 0.000 claims description 13
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 7
- 239000001569 carbon dioxide Substances 0.000 claims description 7
- 238000001816 cooling Methods 0.000 abstract description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 6
- UPHIPHFJVNKLMR-UHFFFAOYSA-N chromium iron Chemical compound [Cr].[Fe] UPHIPHFJVNKLMR-UHFFFAOYSA-N 0.000 abstract description 2
- TVZPLCNGKSPOJA-UHFFFAOYSA-N copper zinc Chemical compound [Cu].[Zn] TVZPLCNGKSPOJA-UHFFFAOYSA-N 0.000 abstract description 2
- 239000007789 gas Substances 0.000 description 40
- 229910002090 carbon oxide Inorganic materials 0.000 description 22
- JFMOYHBEGWPXBI-UHFFFAOYSA-N [C].[As] Chemical compound [C].[As] JFMOYHBEGWPXBI-UHFFFAOYSA-N 0.000 description 4
- 125000004122 cyclic group Chemical group 0.000 description 4
- 239000002918 waste heat Substances 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 208000012839 conversion disease Diseases 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000001784 detoxification Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- LBVWYGNGGJURHQ-UHFFFAOYSA-N dicarbon Chemical compound [C-]#[C+] LBVWYGNGGJURHQ-UHFFFAOYSA-N 0.000 description 1
- 238000003113 dilution method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003546 flue gas Substances 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 230000029052 metamorphosis Effects 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000005192 partition Methods 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
Landscapes
- Carbon And Carbon Compounds (AREA)
- Catalysts (AREA)
- Industrial Gases (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
ナフサやLPGなどの石油系原料をガス叱すると、生成
された都市ガス中には、約20%前後の多量な一酸化炭
素が含有されているので、法規制6%以下にある通り、
これを無毒Cヒする必要がある。[Detailed Description of the Invention] (Industrial Application Field) When petroleum-based raw materials such as naphtha and LPG are gassed, the city gas produced contains a large amount of carbon monoxide, approximately 20%. Therefore, as stated in the legal regulation of 6% or less,
This needs to be treated with non-toxic C.
無毒化は、−酸「ヒ炭素変戊用の鉄系触媒を用いて35
0〜500℃の温度で行う高温変成法、若しくは、銅系
触媒を用いて100〜350’Cの温度で行う低温変成
法による2吠装置を都市ガス製造プラント系内に付設し
て、−酸「ヒ炭素を二酸化炭素に転化変咬して行われて
いる。Detoxification is achieved by using an iron-based catalyst for the conversion of -acid to arsenic carbon.
A high-temperature shift conversion method performed at a temperature of 0 to 500°C or a low-temperature shift conversion method performed at a temperature of 100 to 350'C using a copper-based catalyst is attached to the city gas production plant system. ``This is done by converting arsenic carbon into carbon dioxide.
この発明は、このようなサイクリック式や連続式の都市
ガス製造1ラントにおける一酸化炭素変成法およびその
装置に関するものである。The present invention relates to a carbon monoxide conversion method and apparatus for such cyclic or continuous city gas production.
(従来の技術)
生成された都市ガス中の一酸化炭素を二酸化炭素に転化
する高温変成法は、例えば出願人のなした特開昭58−
157896号に開示された発明があり、低温変成法は
、例えば特公昭63−20277号に開示された発明が
ある。(Prior Art) A high-temperature metamorphosis method for converting carbon monoxide in generated city gas into carbon dioxide is known, for example, from Japanese Patent Application Laid-Open No. 1983-1992, which was made by the applicant.
There is an invention disclosed in Japanese Patent Publication No. 157896, and a low-temperature metamorphism method is disclosed in Japanese Patent Publication No. 63-20277, for example.
ところで、−酸化炭素を二酸化炭素に転化変成する反応
は、発熱を伴う。しかし、上述の発明はいずれも、反応
が行われる触媒層の温に!II整は行われていない。By the way, the reaction of converting -carbon oxide into carbon dioxide is accompanied by heat generation. However, the above inventions all depend on the temperature of the catalyst layer where the reaction takes place! II adjustment has not been performed.
(発明が解決しようとする課題)
従来例の都市ガス製造プラントにおける一酸化炭素変成
法は、反応によって生じる熱が触媒層の温度を適正反応
温度以上に上昇させるので、高効率反応を継続維持する
ことが難しく、更に、触媒自身の強度が弱く自壊により
触媒層をうず高く積み上げて形成することが困難なため
、高効率大容量のガス処理が難しかった。(Problems to be Solved by the Invention) In the conventional carbon monoxide conversion method in city gas production plants, the heat generated by the reaction raises the temperature of the catalyst layer above the appropriate reaction temperature, making it difficult to continue and maintain high efficiency reactions. Moreover, since the strength of the catalyst itself is weak and self-destruction makes it difficult to stack the catalyst layers in a high pile, it has been difficult to process gases with high efficiency and large capacity.
また1反応によって発生した熱も有効利用されることな
く放散していた。Furthermore, the heat generated by one reaction was dissipated without being effectively utilized.
そこで本発明は、大容量の都市ガス中に含まれる一酸f
ヒ炭素を継続した高い反応効率で二酸化炭素に転化変成
し、加えて1反応熱をも回収する都市ガス製造プラント
の一酸化炭素変成法およびその装置を提供するものであ
る。Therefore, the present invention aims to solve the problem of monoacid f contained in a large amount of city gas.
The present invention provides a carbon monoxide conversion method for a city gas production plant and an apparatus for converting carbon monoxide into carbon dioxide with continuous high reaction efficiency and also recovering the heat of one reaction.
(課題を解決するための手段)
この発明は、都市ガス製造プラントの県内に、複R段に
仕切って設けた各一酸化炭素変成用触媒層を間接冷却し
て行う一酸化炭素変成法置を設け、その−酸化炭素変成
装置に都市ガス製造プラントの反応器で生成された多量
の水分と一酸化炭素を含む都市ガスを導入し、有害な一
酸化炭素を二酸化炭素に転化変成せしめて、増熱工程や
希釈工程を経たのち、無毒化された都市ガスを一般供給
しようとするものである。(Means for Solving the Problems) The present invention provides a carbon monoxide shift conversion system in which carbon monoxide shift catalyst layers are partitioned into multiple R stages and are indirectly cooled in a prefecture of a city gas production plant. City gas containing a large amount of moisture and carbon monoxide produced in the reactor of a city gas production plant is introduced into the carbon oxide conversion equipment, and the harmful carbon monoxide is converted into carbon dioxide. The aim is to supply city gas to the public that has been detoxified after undergoing heat and dilution processes.
また、その−酸化炭素変成装置は、生成した都市ガスを
導入する複数段に仕切られた触媒層と、該複数段に仕切
られた触媒層間を直列に接続する経路と、該経路に熱媒
体を通して都市ガスを間接冷却する予熱器とを設けて形
式したものである。In addition, the carbon oxide shift device has a catalyst layer partitioned into multiple stages into which generated city gas is introduced, a path connecting the catalyst layers partitioned into multiple stages in series, and a heat medium passed through the path. This type is equipped with a preheater that indirectly cools city gas.
(作用)
上述の方法により、−酸化炭素を二酸化炭素に転化2戒
する反応から発生する熱は、都市ガスによって搬送され
、各−酸化炭素変改用触媒層間の経路に設けた予熱器に
おいて間接的に冷却されて熱回収されるため、複数段に
仕切られた各触媒層は常に反応に適した温度となり、高
効率の反応を継続維持できる。(Function) By the method described above, the heat generated from the reaction of converting carbon oxide to carbon dioxide is carried by city gas and indirectly heated in a preheater installed in the path between each carbon oxide conversion catalyst layer. Since the catalyst is cooled and heat is recovered, each catalyst layer partitioned into multiple stages is always at a temperature suitable for the reaction, allowing a highly efficient reaction to continue.
また、反応によって各−酸化炭素変成用触媒層において
発生した熱は、予熱器の水や空気又は蒸気の熱媒体によ
って間接冷却され、該熱媒体が得た熱を回収する。この
回収熱は、−酸化炭素の変改に必要とされる水又は蒸気
のプレヒート、つまり予熱に利用したり、都市ガス生成
の反応に必要な蒸気の製造等の熱源に有効に使用する。Further, the heat generated in each carbon oxide conversion catalyst layer due to the reaction is indirectly cooled by a heat medium such as water, air, or steam in a preheater, and the heat obtained by the heat medium is recovered. This recovered heat is effectively used for preheating water or steam required for the conversion of carbon oxide, or as a heat source for producing steam necessary for the reaction of generating city gas.
−酸化炭素変成用触媒層の冷却を、水又は蒸気によって
直接冷却することなく、熱媒体を利用した間接冷却する
ことによって、触媒の損傷を防止し、触媒層は、充填触
媒の損傷による目詰まりを生じることがない。- By indirectly cooling the catalyst layer for carbon oxide conversion using a heat medium without directly cooling it with water or steam, damage to the catalyst can be prevented, and the catalyst layer can be prevented from being clogged due to damage to the packed catalyst. will not occur.
一酸化炭素変成用触媒層を複数段に形式することによっ
て、必要とされる反応後の一酸化炭素濃度の調整が容易
ヒなり、さらに、うず高く形式された触媒層で生じゃす
い漏流やショートバスおよび触媒の自壊は生じない。By forming the carbon monoxide conversion catalyst layer in multiple stages, it is easy to adjust the required carbon monoxide concentration after the reaction, and the undulating catalyst layer also prevents leakage. Short baths and catalyst self-destruction do not occur.
(実施例)
この発明に係るサイクリック式都市ガス製造プラントの
低温−酸化炭素変成法の−の実施例のフローシートを第
1図に示す。(Example) FIG. 1 shows a flow sheet of an example of the low-temperature carbon oxide conversion method for a cyclic city gas production plant according to the present invention.
反応器1において製造された都市ガスは、排熱ボイラー
2で冷却されてガス温度を調節後、低温−酸化炭素変成
器3に導入され、図示省略したが水封器5を出たところ
で熱カロリーの増熱をし、スクラバー6を経た後、熱カ
ロリーの希釈調整をし、その後ガスホルダーに貯蔵され
、都市ガスとして一般供給される。The city gas produced in the reactor 1 is cooled in the waste heat boiler 2 to adjust the gas temperature, and then introduced into the low-temperature carbon oxide shift converter 3. Although not shown, the city gas is converted into heat caloric value after exiting the water sealer 5. After passing through the scrubber 6, the gas is diluted and adjusted for thermal calorie content, and then stored in a gas holder and supplied to the public as city gas.
都市ガスを製造するメーク期は上述の工程で行われ、都
市ガスを製造する反応器を昇温するヒート期は、反応器
1を加温した燃焼排ガスの余熱を排熱ボイラー2で熱回
収された後、排ガスとして煙突7から大気放出される。The make period for producing city gas is carried out by the above-mentioned process, and during the heat period for raising the temperature of the reactor for producing city gas, the residual heat of the flue gas that heated the reactor 1 is recovered by the waste heat boiler 2. After that, it is released into the atmosphere from the chimney 7 as exhaust gas.
このヒート期とメーク期の繰り返し、つまり、サイクリ
ックによって、都市ガスの製造は行われる。City gas is manufactured by repeating this heat period and make period, that is, by cyclically.
低温−酸化炭素変改器3は、まず、−塔を複数段に分割
して仕切り、その各段に一酸化炭素を二数に炭素に転化
変成する一酸化炭素変成用触媒を充填して、触媒層8.
8を形成する。The low-temperature carbon oxide converter 3 first divides and partitions the tower into a plurality of stages, and each stage is filled with a carbon monoxide transformation catalyst that converts carbon monoxide into two carbons. Catalyst layer 8.
form 8.
第11!?lの実施例の場合、低温域100℃から35
0℃程度の温度に適した銅−亜鉛系の低温用触媒を2段
に充填した触媒層8.8を設けて形成したが、高温域3
00℃から500℃程度の温度に適した鉄−クロム系の
高温用触媒を2段に充填した触媒層8.8、若しくは、
上段に高温用触媒、下段に低温用触媒を充填した触媒層
8.8、またはその逆の組合せ、又は、第2図に示すよ
うに触媒層8を3段や、或は、それ以上の多数段に形成
して、各プラントに適した組合せに形成する。11th! ? In the case of Example 1, the low temperature range is from 100°C to 35°C.
Although it was formed by providing a catalyst layer 8.8 packed in two stages with a copper-zinc-based low-temperature catalyst suitable for temperatures around 0°C, the high-temperature region 3
Catalyst layer 8.8 filled with two stages of iron-chromium-based high-temperature catalyst suitable for temperatures from about 00°C to 500°C, or
The catalyst layer 8.8 is filled with a high-temperature catalyst in the upper layer and a low-temperature catalyst in the lower layer, or the reverse combination, or three or more catalyst layers 8 as shown in FIG. Form into stages to form a combination suitable for each plant.
その各触媒層8.8間を直列に接続する経路9設け、そ
の経路9には、−酸fヒ炭素を二数Cヒ炭素に転化変成
する際に生じる反応熱を搬送する都市ガスを間接冷却す
る予熱器4を設け、反応によって昇温した都市ガスを予
熱器4管内に通る空気や水、又は水蒸気の熱媒体によっ
て間接的に冷却をし、都市ガス自体を反応に適した温度
に再び戻すように形成する。A path 9 is provided that connects each of the catalyst layers 8 and 8 in series, and through the path 9, city gas is indirectly supplied which carries the reaction heat generated when converting -acid f arsenic carbon to dicarbon arsenic carbon. A cooling preheater 4 is provided, and the city gas whose temperature has risen due to the reaction is indirectly cooled by a heating medium such as air, water, or steam passing through the preheater 4 pipe, and the city gas itself is brought back to a temperature suitable for the reaction. Form it back.
昇温した都市ガスを間接冷却することによって回収した
熱は、都市ガス製造に使用する蒸気の発生Iを増加する
ための排熱ボイラを予熱する熱、又は、燃焼用空気を予
熱する熱等の熱源として、有効に利用されるや
第1図のフローシートに示されるこの発明に係るサイク
リック式都市ガス製造プラントの二段式低温−酸化炭素
変成装置の装置人口と出口の試験結果の一例を表に示す
。The heat recovered by indirectly cooling the heated city gas can be used as heat for preheating a waste heat boiler to increase the generation of steam used for city gas production, or as heat for preheating combustion air. When used effectively as a heat source, an example of the test results of the device population and outlet of the two-stage low-temperature-carbon oxide shift device of the cyclic city gas production plant according to the present invention shown in the flow sheet of Fig. 1 is shown below. Shown in the table.
表
この場合の反応器1で製造された都市ガスは、排熱ボイ
ラー2を経て冷却され、低温−酸化炭素変成装W3人口
で約180’C程度の温度となり、上段の鋼−亜鉛系触
媒の触媒層8で、−酸化炭素の二rllL(1:、炭素
への一次転化変吠反応を起こして、約240℃程度とな
り、予熱器4で約160℃種変に冷却されて、下段の低
温−酸化炭素変成用触媒の触媒層8に導入され、更に、
二次転化変成反応をして、約260℃の都市ガスとして
、低温−酸化炭素変成装置3出口から導出される。Table: In this case, city gas produced in reactor 1 is cooled through waste heat boiler 2, and reaches a temperature of about 180'C in low-temperature carbon oxide conversion system W3, and the temperature is about 180'C in the low-temperature carbon oxide conversion system W3. In the catalyst layer 8, a primary conversion reaction of -carbon oxide to carbon occurs at about 240°C, which is cooled to about 160°C in the preheater 4 to reach a low temperature in the lower stage. - introduced into the catalyst layer 8 of the carbon oxide conversion catalyst;
A secondary conversion reaction is carried out, and the city gas at about 260° C. is discharged from the outlet of the low-temperature carbon oxide shift device 3.
また、都市ガス中の一酸化炭素は、約21.4%から約
2.5%へと低減されて、転化変成率90%以上という
高効率を維持した。In addition, carbon monoxide in city gas was reduced from about 21.4% to about 2.5%, maintaining a high conversion rate of over 90%.
〈発明の効果)
以上の通りこの発明は、複数段に仕切られた各−酸化炭
素変成用触媒層を常に反応に適した温度に継続維持する
ことができ、更に、反応によって生じた熱を予熱などの
熱源として有効利用するため、高効率で安定したーwI
り炭素の転fヒ変成が可能となり、都市ガス製造プラン
トとしても、耐久性のある設備となり、経済的にも優れ
たものとなる。<Effects of the Invention> As described above, the present invention is capable of continuously maintaining each of the carbon oxide shift catalyst layers partitioned into multiple stages at a temperature suitable for the reaction, and furthermore, the heat generated by the reaction can be used for preheating. Highly efficient and stable as it can be used effectively as a heat source such as
This makes it possible to transmute carbon, making it a durable and economically superior facility for city gas production plants.
また、複数段に仕切られた各−酸化炭素変成用触媒層の
冷却は、間接冷却方式を採用しているため、充填触媒の
破損による目詰まりを生じることなく、メンテナンスが
容易となり、均一で高効率の反応を継続維持することが
できる。In addition, indirect cooling is used to cool each of the carbon oxide shift catalyst layers, which are partitioned into multiple stages, so there is no clogging due to damage to the packed catalyst, and maintenance is easy and the temperature is uniform and high. Efficient reactions can be continuously maintained.
また、無毒化された都市ガスは、ガス利用者の安全に貢
献することとなる。In addition, detoxified city gas will contribute to the safety of gas users.
第1図は、この発明に係る−の実TI&例を示す二段式
低温−酸化炭素変成装置をサイクリック式都市ガス製造
プラントに適用したプロセスフローシートである。第2
図は、−酸化炭素変成用触媒層を3段とした場合の一酸
化炭素変成装買の概略説明図である。
l・・・・反応器 2・・・・排熱ボイラ3・・
・・−酸化炭素変成装置FIG. 1 is a process flow sheet in which a two-stage low-temperature carbon oxide shift apparatus is applied to a cyclic city gas production plant, showing an example of actual TI and oxidation according to the present invention. Second
The figure is a schematic explanatory diagram of a carbon monoxide conversion equipment in which the -carbon oxide conversion catalyst layer is arranged in three stages. l...Reactor 2...Exhaust heat boiler 3...
・・・-Carbon oxide conversion equipment
Claims (2)
間を直列に接続する経路に熱媒体を通して都市ガスを間
接冷却する工程を設けて、反応器で生成された水分を含
有する都市ガス中の一酸化炭素を二酸化炭素に変成する
ことを特徴とする都市ガス製造プラントの一酸化炭素変
成法。(1) A process is provided to indirectly cool city gas by passing a heat medium through a path that connects in series between multiple stages of carbon monoxide conversion catalyst layers that are partitioned, so that city gas containing moisture generated in a reactor can be cooled. A carbon monoxide conversion method for city gas production plants that converts carbon monoxide inside into carbon dioxide.
と、該複数段の触媒層間を直列に接続する経路と、該経
路に熱媒体を利用した熱交換によって都市ガスを間接冷
却する予熱器とを設けたことを特徴とする都市ガス製造
プラントの一酸化炭素変成装置。(2) City gas is indirectly cooled through heat exchange using a plurality of partitioned carbon monoxide conversion catalyst layers, a path connecting the plurality of catalyst layers in series, and a heat medium in the path. A carbon monoxide shift device for a city gas production plant, characterized in that it is equipped with a preheater.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1209709A JP3008295B2 (en) | 1989-08-15 | 1989-08-15 | Carbon monoxide conversion method and equipment for city gas production plant |
Applications Claiming Priority (1)
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JP1209709A JP3008295B2 (en) | 1989-08-15 | 1989-08-15 | Carbon monoxide conversion method and equipment for city gas production plant |
Publications (2)
Publication Number | Publication Date |
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JPH0374493A true JPH0374493A (en) | 1991-03-29 |
JP3008295B2 JP3008295B2 (en) | 2000-02-14 |
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JP1209709A Expired - Fee Related JP3008295B2 (en) | 1989-08-15 | 1989-08-15 | Carbon monoxide conversion method and equipment for city gas production plant |
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2013094512A1 (en) * | 2011-12-22 | 2013-06-27 | 三菱重工業株式会社 | Co shift reaction apparatus and co shift reaction method |
WO2013129086A1 (en) * | 2012-02-27 | 2013-09-06 | 三菱重工業株式会社 | Co-shift reaction device and gasification gas purification system |
-
1989
- 1989-08-15 JP JP1209709A patent/JP3008295B2/en not_active Expired - Fee Related
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2013094512A1 (en) * | 2011-12-22 | 2013-06-27 | 三菱重工業株式会社 | Co shift reaction apparatus and co shift reaction method |
AU2012354919B2 (en) * | 2011-12-22 | 2016-01-21 | Mitsubishi Heavy Industries Engineering, Ltd. | CO shift reaction apparatus and CO shift reaction method |
WO2013129086A1 (en) * | 2012-02-27 | 2013-09-06 | 三菱重工業株式会社 | Co-shift reaction device and gasification gas purification system |
US9238208B2 (en) | 2012-02-27 | 2016-01-19 | Mitsubishi Heavy Industries, Ltd. | CO shift reaction apparatus and gasification gas refining system |
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Publication number | Publication date |
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JP3008295B2 (en) | 2000-02-14 |
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