JPS60200802A - Co converter - Google Patents

Co converter

Info

Publication number
JPS60200802A
JPS60200802A JP5727084A JP5727084A JPS60200802A JP S60200802 A JPS60200802 A JP S60200802A JP 5727084 A JP5727084 A JP 5727084A JP 5727084 A JP5727084 A JP 5727084A JP S60200802 A JPS60200802 A JP S60200802A
Authority
JP
Japan
Prior art keywords
catalyst
cooling
conversion
temperature
gas
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
JP5727084A
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 JP5727084A priority Critical patent/JPS60200802A/en
Publication of JPS60200802A publication Critical patent/JPS60200802A/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 an inner tube packed with a catalyst for high temp. use and an outer tube packed with a catalyst for low temp. use into a single apparatus and by combining the apparatus with a heat exchanger for cooling. CONSTITUTION:Gas for conversion contg. gaseous CO, together with steam, is fed into an inner tube 31 from a gas inlet 37, and it is exchaused from a gas outlet 37' through an outer tube 32. In the inner tube 31, a cooling medium is fed into a group of cooling ipes from the bottom to cool catalyst 34 for the conversion reaction of CO at a high temp., and it is discharged from the top. In the outer tube 32, a cooling medium is fed into a group of cooling pipes from the top to cool a catalyst 35 for the conversion reaction of CO at a low temp., and it is discharged from the bottom. The outer tube 32 is kept at a lower temp. than the inner tube 31.

Description

【発明の詳細な説明】 本発明は、水素製造における炭化水素の水蒸気改質装置
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 The present invention relates to a CO shift converter (also commonly referred to as a CO converter) used in a hydrocarbon steam reformer in hydrogen production.

第1図に、従来の水蒸気改質装置のフロー金示す。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)、3は高温CO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(1)、 (2)で表わされ、通常65
0乃至850℃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), 3 is a high-temperature CO shift device, 4 is a cooling heat exchanger,
5 is a low temperature CO converter. The reaction within the steam reformer is expressed by the following formulas (1) and (2), and is usually 65
It is carried out at a temperature range of 0 to 850°C.

OH4+H20−Co + !lH2・・・・・・(1
)00−1− H,O≠=co2+a2 −・・・・・
(2)炭化水素改質装置1では、主として(1)式で表
わされる反応が、また、高温CO変成装誼3並びに低温
OO変成装置5では、主として(2)式で衣わされる反
応が起る。
OH4+H20-Co+! lH2・・・・・・(1
)00-1- H, O≠=co2+a2 -・・・・・・
(2) In the hydrocarbon reformer 1, the reaction mainly expressed by equation (1) is carried out, and in the high temperature CO shift equipment 3 and low temperature OO shift equipment 5, the reaction mainly expressed by equation (2) is carried out. It happens.

メタンを原料とした場合について、第1図に示す各ライ
ンのガス組成、温度、圧力の一例全下記の表に示す。
In the case where methane is used as a raw material, an example of the gas composition, temperature, and pressure of each line shown in FIG. 1 is shown in the table below.

上記(2)式で表わされるCO変成装置内でのCO転化
(シフト)反応は、発熱反応で69、低温はど右へ反応
が進むので、冷却を必要とする。
The CO conversion (shift) reaction in the CO shift converter expressed by the above equation (2) is an exothermic reaction69, and the reaction proceeds further at low temperatures, so cooling is required.

このため、従来装置では、高温、低温00変成装置3,
5の前に熱交換器2.4を設けて冷却を行なっている。
For this reason, in the conventional equipment, high temperature and low temperature 00 shift equipment 3,
A heat exchanger 2.4 is provided in front of 5 for 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。
When each device is separated in this way, piping, shutoff valves, control valves, etc. are added, and as a result, the entire device becomes complicated.

従来のCO変成装置に、化学プラント用の水蒸気改質装
置に使われるものでおるが、例えば分散型燃料電池等の
少量の水素発生を必要とし、且りCO濃度に制限を特徴
とする特に、小型プラントで、且り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
ものでめり、またコスト高でもめる。
Conventional CO conversion equipment is used in steam reforming equipment for chemical plants, but in particular, it requires a small amount of hydrogen generation, such as distributed fuel cells, and is characterized by restrictions on CO concentration. In small-sized plants that place great emphasis on thermal economy, conventional methods tend to be complicated and thermally uneconomical, and are also costly.

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

すなわち、本発明は、高温用CO転化触媒を充填した円
筒、低温用CO転化触媒を充填した外筒よりなり、夫々
の触媒充填層に個別に調節しうる冷却手段を設け、CO
含肩ガスと水蒸気よりなる混合ガスを前記内筒、外筒の
順に流通させるようにしたことを特徴とするCO変成装
置に関する。
That is, the present invention consists of a cylinder filled with a high-temperature CO conversion catalyst and an outer cylinder filled with a low-temperature CO conversion catalyst.
The present invention relates to a CO converter characterized in that a mixed gas consisting of shoulder gas and water vapor is made to flow through the inner cylinder and the outer cylinder in this order.

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
却機能をもつこと。
(1) Omit an intermediate cooling device and provide a cooling function inside the CO converter.

(2) 同一装置内に、高温、低温00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。
(2) It must have high temperature and low temperature 00 shift devices in the same device, and a cooling function in the CO conversion catalyst layer.

(3)内筒に高温用CO転化触媒を、ま・た外筒に低温
用00転化触媒全充填してなること。
(3) The inner cylinder is fully filled with a high-temperature CO conversion catalyst, and the outer cylinder is fully filled with a low-temperature 00 conversion catalyst.

かかる特徴を有する本発明装置は、水素裏造装置や燃料
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 backing device and a fuel reformer for a fuel cell power generation system.

以下に、本発明装置全第2図に基づき説明する。The entire apparatus of the present invention will be explained below based on FIG. 2.

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

第2図の装置では、内筒31及び外筒32エクなる2重
円筒管に共通の鏡板33が底板としてつけらfL、oo
変成装置本体容器を形成している。内筒31には、高温
CO転化反応用触媒34が入れらn、また、外筒32に
は、低温用CO転化反応用触媒35が入れられ、何れも
目皿36で触媒が支えられている。変成すべき原料ガス
に、ガス人口37より供給され、円筒31内を下降し、
底部空間38を経て外筒32内を上昇し、水素富化状態
でガス出口37′より系外へ排出される。
In the device shown in FIG. 2, a common end plate 33 is attached as a bottom plate to the double cylindrical tube consisting of the inner tube 31 and the outer tube 32.
It forms the main body container of the metamorphic device. The inner cylinder 31 contains a catalyst 34 for high-temperature CO conversion reaction, and the outer cylinder 32 contains a catalyst 35 for low-temperature CO conversion reaction, both of which are supported by perforated plates 36. . The raw material gas to be metamorphosed is supplied from the gas population 37 and descends inside the cylinder 31,
The gas rises inside the outer cylinder 32 through the bottom space 38 and is discharged from the system through the gas outlet 37' in a hydrogen-enriched state.

また、内筒31及び外筒32の内部を貫通して、冷却管
群39.39’が設けられており、触媒層で発生する熱
を吸収し、冷却できるようにされている。冷却媒体とし
ては、気体、液体など回収し几熱金利用しやすいものが
使用される。
Further, cooling pipe groups 39 and 39' are provided penetrating the insides of the inner cylinder 31 and the outer cylinder 32, so that the heat generated in the catalyst layer can be absorbed and cooled. As the cooling medium, gases, liquids, and other materials that can be easily recovered and used as hot metals are used.

COガスを含む変成用ガスは、水蒸気と共にガス入口3
7から内筒31へ入9、底部空間38を介して目皿36
から外筒32ヶ通過し、ガス出口37′から排出される
。−万、冷却媒体は、内筒31では、下部から冷却管群
39へ入り、高温用CO転化反応用触媒34を冷却して
、上部の冷却管群39′へ排出される。又、外筒32で
は、冷却媒体は、上部から冷却管群39へ人、す、低温
用CO転化反応用触媒35′t−冷却して、下部の冷却
管群39′へ排出される。この場合、冷却管群39.3
9’は、内筒31側よりも外筒32側がより低温に保た
れるように配置される。
Converting gas containing CO gas enters the gas inlet 3 together with water vapor.
7 into the inner cylinder 31 9 and the perforated plate 36 via the bottom space 38
The gas passes through 32 outer cylinders and is discharged from the gas outlet 37'. - In the inner cylinder 31, the cooling medium enters the cooling pipe group 39 from the lower part, cools the high temperature CO conversion reaction catalyst 34, and is discharged to the upper cooling pipe group 39'. Further, in the outer cylinder 32, the cooling medium is cooled from the upper part to the cooling pipe group 39, and is then cooled to the low-temperature CO conversion reaction catalyst 35', and then discharged to the lower cooling pipe group 39'. In this case, cooling pipe group 39.3
9' is arranged so that the outer cylinder 32 side is kept at a lower temperature than the inner cylinder 31 side.

即ち、内筒31の高温用CO転化反応には、鉄−クロム
系触媒が使われ、入口部で250〜350℃、出口部で
400〜500℃の冷却系が組まれ、又、外筒32の低
温CO転化反応には、0u−Zn系、0u−Eli系、
0uO−ZnO−At203系等の触媒が使わn、入口
部で100〜150℃、出口部で250〜300℃での
冷却系が組まれる。
That is, an iron-chromium catalyst is used for the high-temperature CO conversion reaction in the inner cylinder 31, and a cooling system is installed at 250 to 350°C at the inlet and 400 to 500°C at the outlet. For the low-temperature CO conversion reaction, 0u-Zn system, 0u-Eli system,
A catalyst such as 0uO-ZnO-At203 system is used, and a cooling system is set up at 100 to 150°C at the inlet and at 250 to 300°C at the outlet.

このようにして転化反応を終え几ガスは、c。After completing the conversion reaction in this way, the phosphorus gas is converted to c.

残留濃度が通常は1%以下にされ、co2とH2及び余
剰の水蒸気を主成分とするガスとなり、外筒32の出口
37′から系外へ排出される。CO転化反応用触媒の交
換に肖っては、上部より吸引方式にて取り出し、再充填
することにより達成可能である。
The residual concentration is usually reduced to 1% or less, and the resulting gas is mainly composed of CO2, H2, and excess water vapor, and is discharged from the system through the outlet 37' of the outer cylinder 32. The CO conversion reaction catalyst can be replaced by taking it out from the top using a suction method and refilling it.

本発明装置では、LNG(メタン)による改質の他、L
PG(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 PG (propane) or methanol is also possible.

本発明により、下記の効果かも几らさnる。The present invention also provides the following effects.

(リ 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t−V効に使用することにより、熱回収が
可能であり、従来の配管等での黒損を防止することがで
きる。
(The heat generated in the reconversion reaction is transferred to the cooling medium,
By using this cooling medium for the t-V effect, heat recovery is possible and black loss in conventional piping can be prevented.

(2)単一機器の中に、高温・低温aO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、弁等全省くことができ、低コストの装置を
供給することができる。
(2) Since the high-temperature/low-temperature aO shift device is incorporated into a single device, and the cooling heat exchangers for each previous stage are combined, piping, valves, etc. can be completely omitted, resulting in low cost. Equipment can be supplied.

(3)円筒に高温用、外筒に低温用のCO転化触媒が夫
々充填され、夫々のaOK成装置に異なつ几冷却媒体、
或は条件の異なる冷却媒体を入れ得るので、反応制御が
容易となる。
(3) The cylinder is filled with a CO conversion catalyst for high temperatures and the outer cylinder is filled with a CO conversion catalyst for low temperatures, and each aOK formation device is filled with a different cooling medium,
Alternatively, since cooling media with different conditions can be introduced, reaction control becomes easier.

【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を示す。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 −
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 -

Claims (1)

【特許請求の範囲】[Claims] 高温用CO転化触媒奮光填した円筒、低温用CO転化触
媒全充填した外筒よりなり、夫々の触媒光填層に個別に
調節しうる冷却手段を設け、00含有ガスと水蒸気より
なる混合ガスを前記内筒、外筒の順に流通させるエラに
したこと全特徴とするCO変成装置。
It consists of a cylinder fully filled with a CO conversion catalyst for high temperatures and an outer cylinder fully filled with a CO conversion catalyst for low temperatures.Each catalyst light filling layer is equipped with a cooling means that can be adjusted individually, and a mixed gas consisting of 00-containing gas and steam is provided. A CO conversion device characterized in that a gill is used to cause the flow to flow through the inner cylinder and the outer cylinder in this order.
JP5727084A 1984-03-27 1984-03-27 Co converter Pending JPS60200802A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5727084A JPS60200802A (en) 1984-03-27 1984-03-27 Co converter

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5727084A JPS60200802A (en) 1984-03-27 1984-03-27 Co converter

Publications (1)

Publication Number Publication Date
JPS60200802A true JPS60200802A (en) 1985-10-11

Family

ID=13050835

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5727084A Pending JPS60200802A (en) 1984-03-27 1984-03-27 Co converter

Country Status (1)

Country Link
JP (1) JPS60200802A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0640705A (en) * 1992-07-23 1994-02-15 Mitsubishi Electric Corp Reactor for fuel cell-type power generator
JPH0664901A (en) * 1992-08-19 1994-03-08 Toshiba Corp Co convertor for fuel cell generating set

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0640705A (en) * 1992-07-23 1994-02-15 Mitsubishi Electric Corp Reactor for fuel cell-type power generator
JPH0664901A (en) * 1992-08-19 1994-03-08 Toshiba Corp Co convertor for fuel cell generating set

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