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JPH08217405A - Fuel reforming system reactor for fuel cell power plant - Google Patents

Fuel reforming system reactor for fuel cell power plant

Info

Publication number
JPH08217405A
JPH08217405A JP7022458A JP2245895A JPH08217405A JP H08217405 A JPH08217405 A JP H08217405A JP 7022458 A JP7022458 A JP 7022458A JP 2245895 A JP2245895 A JP 2245895A JP H08217405 A JPH08217405 A JP H08217405A
Authority
JP
Japan
Prior art keywords
heat transfer
catalyst
reforming system
heater
fuel
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
JP7022458A
Other languages
Japanese (ja)
Inventor
Koichi Kaneko
浩一 金子
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.)
Fuji Electric Co Ltd
Original Assignee
Fuji Electric Co 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 Fuji Electric Co Ltd filed Critical Fuji Electric Co Ltd
Priority to JP7022458A priority Critical patent/JPH08217405A/en
Publication of JPH08217405A publication Critical patent/JPH08217405A/en
Pending legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00Fuel cells; Manufacture thereof
    • H01M8/06Combination of fuel cells with means for production of reactants or for treatment of residues
    • H01M8/0606Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants
    • H01M8/0612Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants from carbon-containing material
    • H01M8/0625Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants from carbon-containing material in a modular combined reactor/fuel cell structure
    • H01M8/0631Reactor construction specially adapted for combination reactor/fuel cell
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/30Hydrogen technology
    • Y02E60/50Fuel cells

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Sustainable Development (AREA)
  • Sustainable Energy (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Devices And Processes Conducted In The Presence Of Fluids And Solid Particles (AREA)
  • Hydrogen, Water And Hydrids (AREA)
  • Fuel Cell (AREA)

Abstract

(57)【要約】 【目的】燃料電池発電プラントにおける燃料改質系の脱
硫器,CO変成器を実施対象に、反応器の起動時には短
時間で触媒を効率よく所定の反応温度に均温加熱できる
ようにした反応器を提供する。 【構成】触媒7を満たした反応容器4の中に触媒昇温用
の棒状電熱ヒータ9を分散配置した反応器において、前
記電熱ヒータに対し、その外周に嵌め合わせた伝熱筒1
0aと、該伝熱筒の周面から放射状に突出したプレート
フィン10bからなる伝熱用フィン10を装着し、その
プレートフィンを周辺の触媒層内へ張り出して伝熱面積
の大きなヒータ/触媒間の熱伝達経路を形成する。
(57) [Abstract] [Purpose] For a fuel reforming system desulfurizer and CO shift converter in a fuel cell power plant, the catalyst is efficiently and uniformly heated to a predetermined reaction temperature in a short time when the reactor is started. Provided is a reactor capable. In a reactor in which rod-shaped electric heaters 9 for heating the catalyst are dispersedly arranged in a reaction container 4 filled with a catalyst 7, a heat transfer tube 1 fitted around the outer periphery of the electric heater.
0a and a heat transfer fin 10 composed of plate fins 10b radially protruding from the peripheral surface of the heat transfer cylinder are mounted, and the plate fins are projected into the peripheral catalyst layer to provide a large heat transfer area between the heater / catalyst. To form a heat transfer path.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、燃料電池発電プラント
の燃料改質系に用いる脱硫器,CO変成器を対象とした
反応器に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a reactor for desulfurizers and CO shifters used in a fuel reforming system of a fuel cell power plant.

【0002】[0002]

【従来の技術】周知のように燃料電池発電プラントで
は、炭化水素系の天然ガス,LPG,ナフサ,都市ガス
などを原燃料として、この原燃料を水素リッチなガスに
改質した上で燃料電池の燃料極に供給して発電を行うよ
うにしており、この燃料改質には一般に水蒸気改質法が
採用されている。この場合に、硫黄分(例えば都市ガス
では付臭剤として有機硫黄化合物を添加している)を含
む燃料の水蒸気改質法では、Ni 系の改質触媒を硫黄に
よる被毒から守るための前処理として脱硫工程が必要で
ある。また、水蒸気改質法により得られた改質ガスには
高濃度(12〜20%)のCOが含まれており、特にリ
ン酸型燃料電池のように電極に白金触媒を用いている場
合には白金触媒をCOによる被毒から防ぐために、後処
理として改質ガスのCO濃度を1%以下に下げるCO変
成工程が必要となる。
2. Description of the Related Art As is well known, in a fuel cell power plant, a hydrocarbon-based natural gas, LPG, naphtha, city gas, etc. is used as a raw fuel, and this raw fuel is reformed into a hydrogen-rich gas before it is used in a fuel cell. The steam reforming method is generally adopted for this fuel reforming. In this case, in the steam reforming method of a fuel containing a sulfur content (for example, an organic sulfur compound is added as an odorant in city gas), it is necessary to protect the Ni-based reforming catalyst from poisoning by sulfur. A desulfurization process is required as a treatment. Further, the reformed gas obtained by the steam reforming method contains a high concentration of CO (12 to 20%), and particularly when a platinum catalyst is used for the electrode as in a phosphoric acid fuel cell. In order to prevent the platinum catalyst from being poisoned by CO, a CO conversion step of reducing the CO concentration of the reformed gas to 1% or less is necessary as a post-treatment.

【0003】図3はかかる水蒸気改質法に基づいた燃料
改質装置の系統図であり、原燃料は脱硫器1,改質器
2,CO変成器3を経て燃料電池の燃料極に供給され
る。ここで、脱硫器1の脱硫工程では、水添触媒(Co
−Mo,Ni−Mo系など)の下で原燃料に水素を添加
し、原燃料に含まれている硫黄分を硫化水素ガスに変え
た後、脱硫触媒(ZnO)との反応により硫化亜鉛に変
えて固定除去するようにしており、その反応温度は20
0〜300℃である。
FIG. 3 is a system diagram of a fuel reformer based on the steam reforming method. Raw fuel is supplied to a fuel electrode of a fuel cell through a desulfurizer 1, a reformer 2 and a CO shifter 3. It Here, in the desulfurization process of the desulfurizer 1, the hydrogenation catalyst (Co
-Mo, Ni-Mo system, etc.), hydrogen is added to the raw fuel to change the sulfur content contained in the raw fuel into hydrogen sulfide gas, and then to zinc sulfide by reaction with a desulfurization catalyst (ZnO). The reaction temperature is 20%.
It is 0 to 300 ° C.

【0004】また、改質器2から出た改質ガス中のCO
成分は、次段の低温用のCO変成器3のおいて、CO変
成触媒(Cu−Zn系)により反応温度200〜300
℃でC02にシフトされる。なお、このシフト反応は発熱
反応である。ところで、オンサイト用の燃料電池発電プ
ラントでは、起動時間をできるだけ早めるために、前記
した燃料改質系の脱硫器1,CO変成器3などを対象と
する反応器に対しては、触媒層の中に伝熱ヒータを分散
配置し、短時間で触媒が活性化する反応温度200〜3
00℃まで昇温させるような方法が一般に採用されてい
る。
In addition, CO in the reformed gas discharged from the reformer 2
In the next-stage low-temperature CO shift converter 3, a component is used at a reaction temperature of 200 to 300 by a CO shift catalyst (Cu-Zn system).
Shifted to C0 2 at ° C. The shift reaction is an exothermic reaction. By the way, in the on-site fuel cell power generation plant, in order to make the start-up time as early as possible, the catalyst layer of the reactor for the desulfurizer 1 of the fuel reforming system 1 and the CO shifter 3 is used. Heat transfer heaters are dispersedly arranged inside, and the reaction temperature is 200 to 3 at which the catalyst is activated in a short time.
A method of raising the temperature to 00 ° C. is generally adopted.

【0005】次に、前記した燃料改質系の反応器のう
ち、CO変成器3を例にその従来構造を図4に示す。図
において、4は反応容器、5は改質ガスのガス導入管,
6はガス出口管、7は触媒、8はCO変成反応に伴う発
熱分を除熱して触媒7を適正な反応温度に維持するため
の冷却用熱交換器、9は起動時に通電して触媒7を常温
から所定の反応温度まで昇温させる電熱ヒータである。
ここで、前記電熱ヒータ9は棒状のヒータ(ヒーズヒー
タ)を用い、該ヒータを裸のまま触媒層の中に突き立て
るようにして複数本のヒータが反応容器1の中に分散配
備されている。
Next, FIG. 4 shows a conventional structure of the CO shift converter 3 as an example of the above-mentioned fuel reforming system reactors. In the figure, 4 is a reaction vessel, 5 is a reformed gas gas introduction pipe,
6 is a gas outlet pipe, 7 is a catalyst, 8 is a cooling heat exchanger for removing heat generated by the CO shift reaction to maintain the catalyst 7 at an appropriate reaction temperature, and 9 is energized at the time of startup to activate the catalyst 7 Is an electric heater for raising the temperature from room temperature to a predetermined reaction temperature.
Here, a rod-shaped heater (heater heater) is used as the electrothermal heater 9, and a plurality of heaters are dispersed and arranged in the reaction vessel 1 such that the heater is pierced into the catalyst layer while being bare.

【0006】また、脱硫器1についても、脱硫触媒を満
たした反応容器の中に前記のCO変成器3と同様な昇温
用の電熱ヒータを装備しており、起動時にはヒータ加熱
により触媒を所定の反応温度(200〜300℃)まで
昇温させ、定常運転時には反応温度を保つように触媒の
温度を検出して電熱ヒータをON/OFF制御するよう
にしている。なお、脱硫器には冷却用の熱交換器が装備
されてない。
The desulfurizer 1 is also equipped with an electric heater for raising the temperature similar to the CO shift converter 3 in a reaction vessel filled with a desulfurization catalyst. The temperature is raised to the reaction temperature (200 to 300 ° C.), and the temperature of the catalyst is detected so as to maintain the reaction temperature during steady operation, and the electric heater is controlled to be turned on / off. The desulfurizer is not equipped with a heat exchanger for cooling.

【0007】[0007]

【発明が解決しようとする課題】ところで、燃料電池発
電プラント用の燃料改質系における脱硫器,CO変成器
の反応器を対象に、前記のように触媒層の中に棒状の電
熱ヒータを直接突き立てて分散配置した従来構造では次
記のような問題点がある。すなわち、電熱ヒータの通電
に伴う発生熱は、まずヒータの表面に直接接する触媒粒
子に伝熱した後、触媒粒子間に次々に伝熱して触媒層全
体を昇温させる。この場合に、電熱ヒータの通電に伴う
表面温度は約500℃になるのに対して、触媒の最高使
用温度は350℃程度である。このために、電熱ヒータ
の表面に直接接している触媒粒子は電熱ヒータから離れ
た位置の触媒粒子に比べて高い温度に加熱される,つま
り高い熱ストレスを受けるために、触媒粒子にシンタリ
ングが生じて寿命が短くなるとともに、触媒粒子が粉化
し易くなって改質ガスを通流させる際の圧損を増加させ
る。また、触媒層内には電熱ヒータを熱源とする大きな
温度勾配が生じて電熱ヒータから離れた位置の触媒粒子
は所定温度まで昇温するのまでに時間的な遅れが生じ、
このために反応器の定常運転が確立するまでの起動時間
が長く掛かる。
By the way, as described above, a rod-shaped electric heater is directly provided in a catalyst layer for a reactor such as a desulfurizer and a CO shifter in a fuel reforming system for a fuel cell power plant. The conventional structure in which they are pushed out and arranged in a distributed manner has the following problems. That is, the heat generated by energization of the electric heater is first transferred to the catalyst particles that are in direct contact with the surface of the heater, and then transferred to the catalyst particles one after another to raise the temperature of the entire catalyst layer. In this case, the surface temperature accompanying energization of the electric heater is about 500 ° C, whereas the maximum operating temperature of the catalyst is about 350 ° C. For this reason, the catalyst particles that are in direct contact with the surface of the electric heater are heated to a higher temperature than the catalyst particles that are located far from the electric heater, that is, because they are subject to high thermal stress, the sintering of the catalyst particles As a result, the life is shortened, and the catalyst particles are easily pulverized to increase the pressure loss when the reformed gas is passed. Further, a large temperature gradient in which the electric heater is used as a heat source is generated in the catalyst layer, and thus the catalyst particles at a position away from the electric heater have a time delay until the temperature rises to a predetermined temperature,
For this reason, it takes a long time until the steady operation of the reactor is established.

【0008】本発明は上記の点にかんがみなされたもの
であり、燃料電池発電プラントに用いる先記の燃料改質
系の脱硫器,CO変成器を実施対象に、起動時には短時
間で触媒を効率よく所定の反応温度に均温加熱できるよ
う改良した燃料電池発電プラント用の燃料改質系反応器
を提供することを目的とする。
The present invention has been made in view of the above points, and the desulfurizer and CO shifter of the above-mentioned fuel reforming system used in a fuel cell power plant are implemented, and the catalyst can be efficiently used in a short time at startup. An object of the present invention is to provide a fuel reforming system reactor for a fuel cell power generation plant, which is improved so that it can be uniformly heated to a predetermined reaction temperature.

【0009】[0009]

【課題を解決するための手段】上記目的を達成するため
に、本発明によれば、触媒を満たした反応容器内に触媒
昇温用の棒状電熱ヒータを分散配置したものにおいて、
前記電熱ヒータの外周に周辺の触媒層内に張り出す伝熱
用フィンを設けて構成するものとする。また、前記構成
における伝熱用フィンは、具体的に次記のような態様で
実施するのがよい。
To achieve the above object, according to the present invention, rod-shaped electric heaters for heating the catalyst are dispersedly arranged in a reaction vessel filled with the catalyst,
A heat transfer fin that projects into the peripheral catalyst layer is provided on the outer periphery of the electric heater. Further, it is preferable that the heat transfer fins in the above-described configuration are specifically implemented in the following modes.

【0010】1)伝熱用フィンを、棒状電熱ヒータの外
周に嵌め合わせた伝熱筒と、該伝熱筒の周面から放射状
に張り出したプレート状フィンとから構成する。 2)前項1)の伝熱筒は、その内径が棒状ヒータの直径
よりも一回り小さく、かつその周上に長手方向のスリッ
トが切欠かれているスリット付き管とする。
1) The heat transfer fin is composed of a heat transfer cylinder fitted to the outer periphery of the rod-shaped electric heater and a plate fin radially extending from the peripheral surface of the heat transfer cylinder. 2) The heat transfer tube of the above item 1) is a tube with a slit whose inner diameter is one size smaller than the diameter of the rod-shaped heater, and a slit in the longitudinal direction is cut out on the circumference.

【0011】[0011]

【作用】前記のように棒状電熱ヒータの外周に伝熱性の
高い金属で作られたフィンを付設することにより、ヒー
タの熱伝達面積が裸のヒータに比べて遥かに大となり、
かつフィンを伝熱媒体として電熱ヒータから離れた位置
の触媒粒子へ熱を直接付与することかできる。したがっ
て、ヒータ加熱時における触媒層内での温度勾配が緩や
かになるので、反応器の起動の際には短時間で効率よく
触媒層全域を所定の反応温度に加熱昇温させることがで
きる。
The heat transfer area of the heater becomes much larger than that of the bare heater by attaching the fin made of metal having high heat conductivity to the outer periphery of the rod-shaped electric heater as described above.
In addition, heat can be directly applied to the catalyst particles at a position apart from the electric heater by using the fin as a heat transfer medium. Therefore, the temperature gradient in the catalyst layer when the heater is heated becomes gentle, so that the entire catalyst layer can be efficiently heated to a predetermined reaction temperature in a short time when the reactor is started.

【0012】また、棒状電熱ヒータの外周に嵌め合わせ
た伝熱筒と、該伝熱筒の周面から放射状に張り出したプ
レート状フィンとからなる伝熱用フィンについて、その
伝熱筒を棒状ヒータの直径よりも一回り小さい内径に選
定したスリット付き管とすることにより、組立ての際に
フィンを電熱ヒータの周面に密着した状態で被着させる
ことができ、これによりヒータ/フィン間の伝熱抵抗を
低く抑えて触媒層との間に高い伝熱性が確保できる。
Further, regarding a heat transfer fin composed of a heat transfer cylinder fitted to the outer periphery of the rod-shaped electric heater and a plate-shaped fin radially protruding from the peripheral surface of the heat transfer cylinder, the heat transfer cylinder is a rod-shaped heater. By using a slitted tube with an inner diameter smaller than the diameter of the heater, the fins can be attached in close contact with the peripheral surface of the electric heater during assembly. The heat resistance can be suppressed to a low level and a high heat transfer property with the catalyst layer can be secured.

【0013】[0013]

【実施例】以下、燃料改質系のCO変成器を例に、本発
明の実施例による反応器の構成を図1,図2に基づいて
説明する。なお、実施例の図中で図4に対応する同一部
材には同じ符号が付してある。すなわち、図示実施例に
おいては、触媒7の中に突き立てて反応容器4の中に分
散配備した棒状の電熱ヒータ9に対して、ヒータ9の外
周に伝熱用フィン10が新たに追加装備されている。こ
の伝熱用フィン10の構造は、図2で示すようにヒータ
9の外周に嵌め合わせた伝熱筒10aと、該伝熱筒10
aの周面から放射方向に張り出した複数枚のプレートフ
ィン10bとからなる。ここで、前記伝熱筒10aは、
その内径がヒータ9の外径よりも一回り小さく、かつそ
の周上一部に長手方向に沿ってスリット10cを切欠い
たスリット付き管であり、該伝熱筒10aを広げた状態
で電熱ヒータ9の外周へ嵌め合わせて密着状態に装着す
る。そして、伝熱用フィン10と組合わせた電熱ヒータ
9を反応容器4に組み込んだ後に容器内に触媒7を充填
する。
EXAMPLES The construction of a reactor according to an example of the present invention will be described below with reference to FIGS. 1 and 2 by taking a CO reformer of a fuel reforming system as an example. In the drawings of the embodiments, the same members corresponding to those in FIG. 4 are designated by the same reference numerals. That is, in the illustrated embodiment, a fin 10 for heat transfer is newly added to the outer periphery of the heater 9 in addition to the rod-shaped electric heater 9 which is pushed into the catalyst 7 and dispersed in the reaction vessel 4. ing. As shown in FIG. 2, the structure of the heat transfer fin 10 includes a heat transfer cylinder 10 a fitted to the outer circumference of the heater 9 and a heat transfer cylinder 10 a.
It is composed of a plurality of plate fins 10b protruding radially from the peripheral surface of a. Here, the heat transfer cylinder 10a is
It is a tube with a slit whose inner diameter is one size smaller than the outer diameter of the heater 9 and in which a slit 10c is cut out along a part of its circumference along the longitudinal direction, and the electrothermal heater 9 with the heat transfer cylinder 10a widened. Fit it to the outer circumference of and fit it tightly. Then, the electrothermal heater 9 combined with the heat transfer fin 10 is assembled in the reaction container 4, and then the catalyst 7 is filled in the container.

【0014】かかる構成により、図1(b)から判るよ
うに、電熱ヒータ9の周囲から放射状に突出したプレー
トフィン10が触媒層の中に張り出してヒータ9と触媒
7との間に伝熱面積の大きな熱伝達経路が確保されるこ
とになる。なお、図示実施例にはCO変成器を示した
が、脱硫器に装備した電熱ヒータについても同様に伝熱
用フィン10を付設して実施するものとする。
With this structure, as can be seen from FIG. 1B, the plate fins 10 radially protruding from the periphery of the electric heater 9 project into the catalyst layer and the heat transfer area between the heater 9 and the catalyst 7 is increased. Will ensure a large heat transfer path. Although the CO converter is shown in the illustrated embodiment, it is assumed that the heat transfer fin 10 is also attached to the electric heater provided in the desulfurizer.

【0015】[0015]

【発明の効果】以上述べたように、本発明の構成によれ
ば、触媒を満たした反応容器内に配置した触媒昇温用の
電熱ヒータに伝熱用フィンを付設したことにより、棒状
の電熱ヒータを裸のまま組み込んだ従来構造と比べて、
次記の効果を奏する。 1)ヒータの伝熱面積が遥かに増大し、伝熱用フィンを
介して電熱ヒータから離れた位置の触媒粒子へ熱を直接
付与することかできる。したがって、ヒータ加熱時にお
ける触媒層内での温度勾配が緩やかになり、反応器の起
動の際には短時間で効率よく触媒層全域を所定の反応温
度に加熱昇温させることができる。
As described above, according to the structure of the present invention, the rod-shaped electrothermal heater is provided by attaching the heat transfer fin to the electrothermal heater for heating the catalyst, which is disposed in the reaction vessel filled with the catalyst. Compared with the conventional structure in which the heater is installed as it is,
It has the following effects. 1) The heat transfer area of the heater is significantly increased, and heat can be directly applied to the catalyst particles located away from the electric heater via the heat transfer fins. Therefore, the temperature gradient in the catalyst layer during heating of the heater becomes gentle, and when the reactor is started, the entire catalyst layer can be efficiently heated to a predetermined reaction temperature in a short time.

【0016】2)電熱ヒータの発生熱が分散して触媒に
伝熱するので、その分だけヒータ近傍の触媒粒子に加わ
る熱ストレスが小さくなり、これにより触媒粒子のシン
タリング,粉化などの触媒劣化を防ぐことができる。 3)また、伝熱用フィンを、棒状電熱ヒータの外周に嵌
め合わせた伝熱筒と、該伝熱筒の周面から放射状に張り
出したプレート状フィンとから構成した上で、その伝熱
筒を棒状ヒータの直径よりも一回り小さい内径に選定し
たスリット付き管とすることにより、組立ての際にフィ
ンを電熱ヒータの周面に密着した状態で被着させること
ができ、これによりヒータ/フィン間の伝熱抵抗を低く
抑えて触媒層との間に高い伝熱性が確保できる。
2) Since the heat generated by the electrothermal heater is dispersed and transferred to the catalyst, the heat stress applied to the catalyst particles in the vicinity of the heater is reduced by that much, whereby the catalyst such as sintering and pulverization of the catalyst particles is reduced. Deterioration can be prevented. 3) Further, the heat transfer fin is composed of a heat transfer tube fitted to the outer periphery of the rod-shaped electric heater, and a plate-shaped fin radially protruding from the peripheral surface of the heat transfer tube. By using a slit tube with an inner diameter slightly smaller than the diameter of the rod-shaped heater, the fins can be attached in close contact with the peripheral surface of the electric heater during assembly. The heat transfer resistance between them can be suppressed low, and high heat transfer can be secured between the catalyst layer and the catalyst layer.

【図面の簡単な説明】[Brief description of drawings]

【図1】燃料改質系のCO変成器を対象とした本発明の
実施例による反応器の構成図であり、(a)は反応器の
縦断面図、(b)は横断面図
FIG. 1 is a configuration diagram of a reactor according to an embodiment of the present invention for a CO reformer of a fuel reforming system, where (a) is a longitudinal sectional view of the reactor and (b) is a transverse sectional view thereof.

【図2】図1におけるフィン付き電熱ヒータの組立構造
を示す斜視図
FIG. 2 is a perspective view showing an assembly structure of the electric heater with fins shown in FIG.

【図3】燃料電池発電プラントにおける燃料改質系の構
成図
FIG. 3 is a block diagram of a fuel reforming system in a fuel cell power plant.

【図4】燃料改質系のCO変成器を対象とした従来にお
ける反応器の構成図であり、(a)は反応器の縦断面
図、(b)は横断面図
4A and 4B are configuration diagrams of a conventional reactor intended for a CO reformer of a fuel reforming system, in which FIG. 4A is a vertical sectional view of the reactor, and FIG.

【符号の説明】[Explanation of symbols]

4 反応容器 7 触媒 9 電熱ヒータ 10 伝熱用フィン 10a 伝熱筒 10b プレートフィン 10c スリット 4 Reaction Container 7 Catalyst 9 Electric Heater 10 Heat Transfer Fin 10a Heat Transfer Tube 10b Plate Fin 10c Slit

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】燃料電池発電プラントの燃料改質系に用い
る脱硫器,CO変成器を対象とした反応器であり、触媒
を満たした反応容器内に触媒昇温用の棒状電熱ヒータを
分散配置したものにおいて、前記電熱ヒータの外周に周
辺の触媒層内に張り出す伝熱用フィンを設けたことを特
徴とする燃料電池発電プラント用の燃料改質系反応器。
1. A reactor intended for a desulfurizer and a CO shifter used in a fuel reforming system of a fuel cell power plant, wherein rod-shaped electric heaters for heating the catalyst are dispersedly arranged in a reaction vessel filled with the catalyst. A fuel reforming system reactor for a fuel cell power plant, wherein heat transfer fins projecting into a peripheral catalyst layer are provided on the outer periphery of the electric heater.
【請求項2】請求項1記載の燃料改質系反応器におい
て、伝熱用フィンが棒状ヒータの外周に嵌め合わせた伝
熱筒と、該伝熱筒の周面から放射状に張り出したプレー
ト状フィンとからなることを特徴とする燃料電池発電プ
ラント用の燃料改質系反応器。
2. The fuel reforming system reactor according to claim 1, wherein a heat transfer fin is fitted to the outer periphery of a rod-shaped heater, and a plate-like member radially extending from the peripheral surface of the heat transfer cylinder. A fuel reforming system reactor for a fuel cell power plant, comprising a fin.
【請求項3】請求項2記載の燃料改質系反応器におい
て、伝熱筒はその内径が棒状ヒータの直径よりも一回り
小さく、かつその周上に長手方向のスリットが切欠かれ
ているスリット付き管としてなることを特徴とする燃料
電池発電プラント用の燃料改質系反応器。
3. The fuel reforming system reactor according to claim 2, wherein the heat transfer cylinder has an inner diameter slightly smaller than the diameter of the rod-shaped heater, and a slit in the longitudinal direction is cut out on the circumference thereof. A fuel reforming system reactor for a fuel cell power plant, which is provided with an attached tube.
JP7022458A 1995-02-10 1995-02-10 Fuel reforming system reactor for fuel cell power plant Pending JPH08217405A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7022458A JPH08217405A (en) 1995-02-10 1995-02-10 Fuel reforming system reactor for fuel cell power plant

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7022458A JPH08217405A (en) 1995-02-10 1995-02-10 Fuel reforming system reactor for fuel cell power plant

Publications (1)

Publication Number Publication Date
JPH08217405A true JPH08217405A (en) 1996-08-27

Family

ID=12083274

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7022458A Pending JPH08217405A (en) 1995-02-10 1995-02-10 Fuel reforming system reactor for fuel cell power plant

Country Status (1)

Country Link
JP (1) JPH08217405A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000048261A1 (en) * 1999-02-10 2000-08-17 Kabushiki Kaisha Toshiba Carbon monoxide converting apparatus for fuel cell and generating system of fuel cell
US6582667B1 (en) 1998-09-18 2003-06-24 Nippon Shokubai Co., Ltd. Shell-and-tube reactor
JP2004525484A (en) * 2000-12-05 2004-08-19 テキサコ ディベラップメント コーポレイション Apparatus and method for heating a catalyst for starting a compact fuel processor
JP2010235406A (en) * 2009-03-31 2010-10-21 Toyota Industries Corp Reformer
WO2012132997A1 (en) * 2011-03-25 2012-10-04 Jx日鉱日石エネルギー株式会社 Desulfurizer

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6582667B1 (en) 1998-09-18 2003-06-24 Nippon Shokubai Co., Ltd. Shell-and-tube reactor
WO2000048261A1 (en) * 1999-02-10 2000-08-17 Kabushiki Kaisha Toshiba Carbon monoxide converting apparatus for fuel cell and generating system of fuel cell
JP2004525484A (en) * 2000-12-05 2004-08-19 テキサコ ディベラップメント コーポレイション Apparatus and method for heating a catalyst for starting a compact fuel processor
JP2010235406A (en) * 2009-03-31 2010-10-21 Toyota Industries Corp Reformer
WO2012132997A1 (en) * 2011-03-25 2012-10-04 Jx日鉱日石エネルギー株式会社 Desulfurizer

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