JPS60200801A - Co converter - Google Patents

Co converter

Info

Publication number
JPS60200801A
JPS60200801A JP5726984A JP5726984A JPS60200801A JP S60200801 A JPS60200801 A JP S60200801A JP 5726984 A JP5726984 A JP 5726984A JP 5726984 A JP5726984 A JP 5726984A JP S60200801 A JPS60200801 A JP S60200801A
Authority
JP
Japan
Prior art keywords
conversion
temperature
gas
catalyst
converter
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
JP5726984A
Other languages
Japanese (ja)
Inventor
Motohei Katsuta
勝田 基平
Kenichi Hisamatsu
健一 久松
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.)
Mitsubishi Heavy Industries Ltd
Original Assignee
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 Mitsubishi Heavy Industries Ltd filed Critical Mitsubishi Heavy Industries Ltd
Priority to JP5726984A priority Critical patent/JPS60200801A/en
Publication of JPS60200801A publication Critical patent/JPS60200801A/en
Pending legal-status Critical Current

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  • Hydrogen, Water And Hydrids (AREA)

Abstract

PURPOSE:To simplify a converter and to reduce the cost by incorporating a catalyst for the conversion of CO at a high temp. and a catalyst for the conversion of CO at a low temp. into a single apparatus in series and by combining the apparatus with a heat exchanger for cooling. CONSTITUTION:Gas for conversion contg. gaseous CO, together with stream, is fed into the body of a converter in the direction of an arrow I, and it is converted into gas contg. CO2, H<2> and excess steam as principal components in beds 25 packed with a catalyst for the conversion of CO at a high temp. and beds 25' packed with a catalyst for the conversion of Co at a low temp. The resulting gas is exchausted from the system in the direction of an arrow II. A cooling medium is fed for the an inlet 21 to cool the beds 25', 25, and it is discharged from an outlet 23.

Description

【発明の詳細な説明】 気改質装置に用いられるCO変成装置(通常は、Co 
コンバータとも呼ばれる)に関する。
DETAILED DESCRIPTION OF THE INVENTION A CO shift converter (usually a CO converter) used in a gas reformer
(also called converter).

第1図に、従来の水蒸気改質装置のフローを示す。第1
図において、1は炭化水素改質装置、2は熱交換器(冷
却器)、6は高温00変成装置、4は冷却用熱交換器、
5は低温CO変成装置である。水蒸気改質装置内での反
応は、下記の式(11, +21で表わされ、通常65
0乃至850Uの温度範囲で行なわれる。
FIG. 1 shows the flow of a conventional steam reformer. 1st
In the figure, 1 is a hydrocarbon reformer, 2 is a heat exchanger (cooler), 6 is a high temperature 00 shift equipment, 4 is a cooling heat exchanger,
5 is a low temperature CO converter. The reaction in the steam reformer is expressed by the following formula (11, +21, usually 65
It is carried out in a temperature range of 0 to 850U.

CH4+ H20二2co + 3H, −’ − −
 +11co+1(、o=亡002+H2 ・・・(2
)炭化水素改質装置1では、王として(1)式で表わさ
れる反応が、また、高温Co変成装置6並びに低温CO
変成装置5では、主として(2)式で表わされる反応が
起る。
CH4+ H202co + 3H, -' - -
+11co+1(,o=death002+H2...(2
) In the hydrocarbon reformer 1, the reaction expressed by equation (1) is also carried out in the high-temperature Co shift converter 6 and the low-temperature CO
In the metamorphic device 5, a reaction mainly expressed by equation (2) occurs.

メタン?原料とした場合について、第1図に上記(2)
式で表わ烙れるCOZ成装置内での00転化(シフト)
反応は、発熱反応であり、低温はど右へ反応が進むので
、冷却全必要とする。
methane? In the case of using it as a raw material, the above (2) is shown in Figure 1.
00 conversion (shift) in the COZ production equipment expressed by the formula
The reaction is exothermic and progresses faster at lower temperatures, so cooling is required.

このため、従来装置では、高温、低温CO変成装置6,
5の前に熱交換器2,4を設けて冷却全行なっている。
For this reason, in the conventional equipment, high temperature and low temperature CO transformation equipment 6,
Heat exchangers 2 and 4 are provided in front of 5 to perform all cooling.

このように各機器が分かれることにより、配管、しめき
、り弁、制御弁などが付加される結果、装置全体が複雑
となってしまう。
By separating each device in this way, piping, shutoff valves, control valves, etc. are added, resulting in the overall device becoming complicated.

従来のCO変成装置は、化学プラント用の水蒸気改質装
置に使われるものであるが、例えば分散型燃料電池等の
/〆量の水素発生全必要とし、且つCOa度に制限全必
要とする。特に、小型プラントで、且つ熱経済全重視す
るプラントでは、従来の方式では、複雑かつ熱的に不経
済なものであり、またコスト高でもある。
Conventional CO shift converters are used in steam reformers for chemical plants, but they require the production of a certain amount of hydrogen, such as a distributed fuel cell, and are limited to the degree of COa. In particular, in small-sized plants that place great emphasis on thermal economy, conventional methods are complex and thermally uneconomical, and are also costly.

本発明は、上記従来の装置の欠点を解消したCO変成装
置を提供するものである。
The present invention provides a CO transformation device that eliminates the drawbacks of the conventional devices described above.

すなわち、本発明は、シェル・アンド・チューブ型熱交
換器のシェル側上下方向に、高温用CO転化触媒及び低
温用CO転化触媒の分割充填区域を設け、高温用00転
化触媒金充填したシェル側には、CO含有ガスと水蒸気
よりなる混合ガス供給部を、低温用CO転化触媒?充填
したシェル側には転化ガス出口部?設け、更に、チュー
ブvcは、ガスの流れとは向流するように冷媒を通ずる
ように冷媒入口部と冷媒出口部を設けたこと全特徴とす
るCO変成装置に関する。
That is, the present invention provides divided filling areas of a high-temperature CO conversion catalyst and a low-temperature CO conversion catalyst in the vertical direction on the shell side of a shell-and-tube heat exchanger, and a high-temperature 00 conversion catalyst gold-filled shell side A mixed gas supply section consisting of a CO-containing gas and water vapor is connected to a low-temperature CO conversion catalyst. Is there a converted gas outlet on the filled shell side? The present invention relates to a CO converter, further characterized in that the tube VC has a refrigerant inlet and a refrigerant outlet for passing the refrigerant in countercurrent flow to the gas flow.

本発明装置では、以下の点を特徴とする。The device of the present invention is characterized by the following points.

(1) 中間の冷却装置を省き、CO変成装置内部に冷
却機能全もつこと。
(1) Eliminate the intermediate cooling device and have all the cooling functions inside the CO converter.

(2) 同一装置内に、高温、低温側CO変成装置を有
し、かつCO転化触媒層内に冷却機能をもつこと、並び
に高温、低温側CO転化用触媒は、充填体粒子?介して
連続していること。
(2) The high temperature and low temperature side CO conversion devices are included in the same device, and the CO conversion catalyst layer has a cooling function, and the high temperature and low temperature side CO conversion catalysts are packed particles? Continuous through.

かかる特徴を有する本発明装置は、水素製造装置や燃料
電池発電システム用燃料改質装置に適用できる。
The device of the present invention having such characteristics can be applied to a hydrogen production device or a fuel reformer for a fuel cell power generation system.

以下に、本発明装置を第2図に基づき説明する。The apparatus of the present invention will be explained below with reference to FIG.

第2図は、本発明のOO変成装置の構成の概要を示す。FIG. 2 shows an outline of the configuration of the OO transformation device of the present invention.

第2図において、20は00変成装置本体容器である。In FIG. 2, 20 is the 00 converter main body container.

21は冷却媒体の導入管ヘッダーであり、22で示す管
群が連結されており、冷却媒体は上部の排出管ヘッダー
25にて系外へ取り出されている。CO変成装置本体容
器20の内部には、棚24があり、この上に触媒25.
25’が充填されている。変成される原料ガスは、矢印
■エタ供給され、矢印■より水素富化状態で排出される
。触媒25.25’は、上下に高温用25、低温用25
′が充填され、その中間には、必要に応じて転化反応に
は関係のない充填物26で仕切られている。また、必要
により、冷却管群は高温用、低温用に2段に設けること
も可能で6’)、この場合には、冷却媒体も2通りに変
えて使うことができる。
Reference numeral 21 designates a cooling medium introduction pipe header, to which a group of pipes shown at 22 are connected, and the cooling medium is taken out of the system through an upper discharge pipe header 25. Inside the CO converter main body container 20, there is a shelf 24, on which a catalyst 25.
25' is filled. The raw material gas to be metamorphosed is supplied as shown in the arrow (■) and is discharged from the arrow (2) in a hydrogen-enriched state. Catalyst 25.25' has 25 for high temperature and 25 for low temperature on top and bottom.
', and the middle thereof is partitioned, if necessary, with a packing 26 not related to the conversion reaction. Furthermore, if necessary, the cooling tube group can be provided in two stages, one for high temperature and one for low temperature 6'), and in this case, the cooling medium can also be used in two different ways.

COガスを含む変成用ガスが水蒸気と共に矢印lより装
置本体に入り、冷却媒体はヘッダ21よジ触媒層25’
、25全冷却して、上部ヘッダー25より加熱されて排
出される。また、冷却用管群22が上下・2段にある場
合には、上段よりも下段がより低温に保たれるよう配置
される。即ち、上段の高温CO転化反応には、鉄−クロ
ム系触媒が使われ、入口部で2.50〜350℃、出口
部で400へ500℃の冷却系が組まれる。また、下段
の低温CO転化反応には、cu−zn系、0u−8i系
、OuO−ZnO−Altos系等の触媒が使われ、入
口部で100〜150℃、出口部で250〜500℃で
の冷却系が組まれる。
Converting gas containing CO gas enters the main body of the device along with water vapor from arrow l, and the cooling medium flows through the header 21 and the catalyst layer 25'.
, 25 is completely cooled, heated and discharged from the upper header 25. Further, when the cooling tube group 22 is arranged in two stages, upper and lower, the lower stage is arranged so as to be kept at a lower temperature than the upper stage. That is, an iron-chromium catalyst is used for the high-temperature CO conversion reaction in the upper stage, and a cooling system is installed at 2.50 to 350°C at the inlet and 400 to 500°C at the outlet. In addition, catalysts such as cu-zn, Ou-8i, and OuO-ZnO-Altos are used for the low-temperature CO conversion reaction in the lower stage, and the temperature is 100 to 150°C at the inlet and 250 to 500°C at the outlet. A cooling system will be installed.

転化反応を終えたガスは、CO残留濃度が通常は1%以
下にされ、CO,とH2及び余剰の水蒸気を主成分とす
るガスとなり、矢印lIより系外へ排出される。CO転
化触媒の交換に当っては、上部エリ吸引方式にて取り出
し、再充填することに工9達成可能である。
The gas that has completed the conversion reaction has a CO residual concentration of usually 1% or less, becomes a gas whose main components are CO, H2, and excess water vapor, and is discharged from the system via arrow lI. When replacing the CO conversion catalyst, step 9 can be achieved by taking it out using the upper area suction method and refilling it.

本発明装置では、LNG (メタン)による改質の他、
LPG (プロパン)やメタノールによる改質も可能で
ある。
In addition to reforming with LNG (methane), the device of the present invention
Modification using LPG (propane) or methanol is also possible.

本発明に、cv、下記の効果がもたらされる。The present invention brings about the following effects.

(1)転化反応で発生する熱が、冷却媒体に移行され、
この冷却媒体を有効に使用することによジ、熱回収が可
能であり、従来の配管等での熱損を防止することができ
る。
(1) The heat generated in the conversion reaction is transferred to the cooling medium,
By effectively using this cooling medium, heat can be recovered, and heat loss in conventional piping can be prevented.

(2)単一機器の中に、高温・低温CO変成装置が組み
込まれ、かつ各前段の冷却用熱交換器が併合されている
ので、配管、弁等を省くことができ、低コストの装置全
供給することができる。
(2) Since the high-temperature and low-temperature CO transformation equipment is incorporated into a single device, and the cooling heat exchangers for each previous stage are combined, piping, valves, etc. can be omitted, resulting in a low-cost device. All can be supplied.

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

第1図は、従来の水蒸気改質装置のフロー金示す。第2
図は、本発明のCO変成装置の構成の概要図である。 復代理人 内 1) 明 復代理人 萩 原 亮 − 第1区
FIG. 1 shows the flow of a conventional steam reformer. Second
The figure is a schematic diagram of the configuration of a CO metamorphosis device of the present invention. Sub-agents 1) Meifuku agent Ryo Hagiwara - 1st ward

Claims (1)

【特許請求の範囲】[Claims] シェル・アンド・チューブ型熱交換器のシェル側上下刃
向に、高温用CO転化触媒及び低温用CO転化触媒の分
割充填区域を設け、高温用CO転化触媒全充填したシェ
ル側には、CO含有ガスと水蒸気よジなる混合ガス供給
部を、低温用CO転化触媒を充填したシェル側には転化
ガス出口部を設け、更に、チューブには、ガスの流れと
は向流するように冷媒を通ずるように冷媒入口部と冷媒
出口部を設けたこと?特徴とするCO変成装置。
The shell side of the shell-and-tube heat exchanger has separate filling areas for high-temperature CO conversion catalysts and low-temperature CO conversion catalysts on the upper and lower sides of the shell side, and the shell side, which is fully filled with high-temperature CO conversion catalysts, contains CO-containing A mixed gas supply section consisting of gas and water vapor is provided, and a converted gas outlet section is provided on the shell side filled with a low-temperature CO conversion catalyst, and a refrigerant is passed through the tube so as to flow countercurrently to the gas flow. Have you provided a refrigerant inlet and a refrigerant outlet? Characteristics of CO metamorphosis equipment.
JP5726984A 1984-03-27 1984-03-27 Co converter Pending JPS60200801A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5726984A JPS60200801A (en) 1984-03-27 1984-03-27 Co converter

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5726984A JPS60200801A (en) 1984-03-27 1984-03-27 Co converter

Publications (1)

Publication Number Publication Date
JPS60200801A true JPS60200801A (en) 1985-10-11

Family

ID=13050807

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5726984A Pending JPS60200801A (en) 1984-03-27 1984-03-27 Co converter

Country Status (1)

Country Link
JP (1) JPS60200801A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002053491A3 (en) * 2000-12-28 2002-09-26 Ballard Power Systems Shell and tube reactor
JP2005247684A (en) * 2004-03-01 2005-09-15 Haldor Topsoe As Method for cooling exothermic reaction zone and reactor unit
JP2008088033A (en) * 2006-10-04 2008-04-17 Sanyo Electric Co Ltd Fuel reforming apparatus

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002053491A3 (en) * 2000-12-28 2002-09-26 Ballard Power Systems Shell and tube reactor
GB2389544A (en) * 2000-12-28 2003-12-17 Ballard Power Systems Shell and tube reactor
JP2005247684A (en) * 2004-03-01 2005-09-15 Haldor Topsoe As Method for cooling exothermic reaction zone and reactor unit
JP2008088033A (en) * 2006-10-04 2008-04-17 Sanyo Electric Co Ltd Fuel reforming apparatus

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