JPS63291802A - Fuel reforming apparatus - Google Patents
Fuel reforming apparatusInfo
- Publication number
- JPS63291802A JPS63291802A JP62125894A JP12589487A JPS63291802A JP S63291802 A JPS63291802 A JP S63291802A JP 62125894 A JP62125894 A JP 62125894A JP 12589487 A JP12589487 A JP 12589487A JP S63291802 A JPS63291802 A JP S63291802A
- Authority
- JP
- Japan
- Prior art keywords
- reforming
- fuel reformer
- gas flow
- gas
- flow path
- 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
Links
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M8/00—Fuel cells; Manufacture thereof
- H01M8/06—Combination of fuel cells with means for production of reactants or for treatment of residues
- H01M8/0606—Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants
- H01M8/0612—Combination 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
- H01M8/0625—Combination 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
- H01M8/0631—Reactor construction specially adapted for combination reactor/fuel cell
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/24—Stationary reactors without moving elements inside
- B01J19/248—Reactors comprising multiple separated flow channels
- B01J19/249—Plate-type reactors
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J8/00—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
- B01J8/02—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds
-
- 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
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/30—Hydrogen technology
- Y02E60/50—Fuel cells
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Sustainable Development (AREA)
- Sustainable Energy (AREA)
- Manufacturing & Machinery (AREA)
- Engineering & Computer Science (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Life Sciences & Earth 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】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、炭化水素やメタノールなどのアルコール類を
水蒸気改質して水素を生成する燃料改質装置に係り、特
に、オンサイト型の燃料電池や半導体製造プロセス向は
純水素製造装置に好適な燃料改質装置に関する。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a fuel reformer that generates hydrogen by steam reforming hydrocarbons and alcohols such as methanol, and particularly relates to an on-site fuel reformer. The field for battery and semiconductor manufacturing processes relates to a fuel reformer suitable for pure hydrogen production equipment.
従来の燃料改質装置は、特開昭53−78983の号公
報の例に代表されるように、改質触媒を反応管に充填し
て改質触媒層を形成し、この反応管を周囲から燃焼ガス
や熱媒体により加熱する外熱方式が主であった。この反
応管型の従来方式では、多数の反応管を配置した反応部
と反応管を加熱する燃焼ガスや高温の熱媒体を得るため
の燃焼部が独立しているため1反応管の周囲には燃焼ガ
スなどの加熱媒体の流路を確保する必要があった。この
ため、オンサイト用として求められる改質装置の小型化
のためには反応管を効率的に配置し、加熱用のガスや熱
媒体の流路による空間を小さくすることが必要であった
。さらに、効率的に反応管を加熱するため反応管周囲の
ガス流路に燃焼触媒を充填し、反応管の周囲で直接燃焼
し高温を得る方式の例として特開昭59−185906
号公報がある。ただし、このような方式でも反応管を改
質触媒層として使用する限り、幾何学的に細密に配置し
ても余剰空間が出来ることはさけられず、小型化に対し
て限界が生じる。また、このような改質装置は単独で使
用されることがほとんどなく、燃料電池など、改質シス
テムの一部として使用されることが多い。このため、高
温装置である燃料改質装置は、外部に多くの熱回収用の
熱交換器を配置し改質システムを構成する必要がある。Conventional fuel reformers, as typified by the example in Japanese Patent Application Laid-open No. 78983/1983, fill a reaction tube with a reforming catalyst to form a reforming catalyst layer, and remove this reaction tube from the surroundings. The main method was external heat heating using combustion gas or heat medium. In this conventional reaction tube type system, the reaction section where many reaction tubes are arranged and the combustion section for obtaining combustion gas and high temperature heat medium to heat the reaction tubes are independent, so there is no space around one reaction tube. It was necessary to secure a flow path for heating medium such as combustion gas. Therefore, in order to downsize the reformer required for on-site use, it is necessary to efficiently arrange the reaction tubes and reduce the space occupied by the flow paths for heating gas and heat medium. Furthermore, in order to efficiently heat the reaction tube, a combustion catalyst is filled in the gas flow path around the reaction tube, and the combustion catalyst is directly combusted around the reaction tube to obtain a high temperature.
There is a publication. However, even in such a system, as long as the reaction tube is used as a reforming catalyst layer, surplus space will inevitably be created even if the reaction tube is arranged geometrically minutely, and there will be a limit to miniaturization. Further, such a reformer is rarely used alone, but is often used as part of a reforming system such as a fuel cell. For this reason, the fuel reformer, which is a high-temperature device, requires many heat exchangers for heat recovery to be disposed outside to form a reforming system.
しかも、改質装置自身の熱回収は、従来の反応管型の装
置では、第2図に示すように、反応管内に改質ガスの戻
り部を設けた熱回収程度しか考慮していなかった。Moreover, in the conventional reaction tube type apparatus, as shown in FIG. 2, the heat recovery of the reformer itself has only been considered to the extent that a reformed gas return section is provided in the reaction tube.
従来の反応管型の燃料改質装置では、装置の小型化の要
求に対して反応管配置の細密化により幾何学的にできる
余剰空間を無くすことはできず、反応管型改質装置の小
型化には限界がある。また、反応管の加熱を良くするた
め、反応管周囲に燃焼触媒を充填q加熱源を反応管に近
づける工夫を考えられているが、燃焼触媒の充填空間の
確保のため単純に細密配置することは難しい。しかも、
燃焼触媒を使用する場合、実際には余剰空間部にも触媒
が充填されてしまうため、必要量以上の触媒を要するこ
とになる。また、従来装置では、触媒反応を主目的にし
ているため、装置構造に対する熱回収の構造は本質的問
題としてほとんど考慮されていない。しかし、最近の改
質装置はシステム全体としてのコンパクト化も求められ
ており、改質装置自体に熱回収機能を付加し易い構造が
必要である。In conventional reaction tube type fuel reformers, it is not possible to eliminate the surplus space created geometrically by making the reaction tube arrangement more compact in response to the demand for smaller devices. There are limits to this. In addition, in order to improve the heating of the reaction tube, it has been considered to fill the area around the reaction tube with a combustion catalyst and move the heat source closer to the reaction tube, but in order to ensure the space for filling the combustion catalyst, it is difficult to simply arrange it closely. is difficult. Moreover,
When a combustion catalyst is used, the excess space is actually filled with catalyst, so a larger amount of catalyst than is required is required. Furthermore, since the main purpose of the conventional apparatus is catalytic reaction, the structure of heat recovery with respect to the apparatus structure is hardly considered as an essential issue. However, recent reformers are required to be more compact as a whole system, and the reformer itself needs a structure that allows it to easily add a heat recovery function.
本発明の目的は、燃料改質装置を含めて改質システムの
コンパクト化を図ることが可能となる燃料改質装置を提
供することにある。An object of the present invention is to provide a fuel reformer that allows the reforming system including the fuel reformer to be made more compact.
上記目的は、改質触媒を隔壁によって区切った層状の空
間に充填する触媒層構造にし、これら層状の改質触媒層
の間に加熱部として高温ガスの発生、あるいは、通過す
る層状の流路を改質触媒層と同様に設け、全体として積
層構造の改質装置構造にすることで、余剰空間を排除し
、さらにこれらの外側に同じく隔壁で区切られたガス流
路を付加し、ここでは改質装置の熱を必要とするシステ
ム内の流体との熱交換を行うのに好適な流路構造を作る
。こうして燃料改質装置は、熱交換器の機能をもつ複合
装置となり、装置の小型化とともにシステムのコンパク
ト化を達成できる。The above purpose is to create a catalyst layer structure in which the reforming catalyst is packed in a layered space separated by partition walls, and between these layered reforming catalyst layers, there is a layered flow path where high-temperature gas is generated or passes through as a heating section. The reformer is provided in the same way as the reforming catalyst layer, and the overall structure of the reformer is a laminated structure, eliminating excess space. Furthermore, a gas flow path separated by a partition wall is added to the outside of the reformer. Create a flow path structure suitable for heat exchange with fluids in the heat-requiring system of the quality device. In this way, the fuel reformer becomes a composite device having the function of a heat exchanger, and it is possible to achieve miniaturization of the device and the system.
改質触媒を隔壁で区切られた層状の空間に充填して改質
触媒層を形成し、この改質触媒層の加熱部を同様に層状
の流路空間で構成することは・、これらを、積層して一
つの改質装置とすることができる。しかも、受熱体とな
る改質触媒層と加熱部を交互に配置して積層することに
より、発熱部の熱を外部への熱損失がなく有効に反応部
である改質触媒層に伝えることができる。また、積層構
造では、反応管型装置のように余剰空間がないため、積
層数を増やし装置の処理容量を増加しても、余剰空間の
増加はなく、常に、必要最小限の大きさが保たれる。更
に、このような積層構造の改質装置は、プレート型熱交
換器相当の熱回収部を改質装置本体の機能を損なうこと
なく、容易に付加することができる。この熱回収部は、
各触媒層の形成と同様に隔壁で区切った流路を改質装置
本体に設けるだけであり、本質的に改質装置の構造は変
わらない、しかし、ここに設けた流路には、改質装置自
身で発生する高温の燃焼排ガスや改質ガスを熱源として
流入させ、改質原料や燃焼用空気を熱回収の低熱源とし
て使用することができる。このような熱回収は従来、改
質装置外部に設けた熱交換器により行われていたが、本
構造の改質装置では、これらの機能を装置本体だけで満
足してしまうため、改質装置周囲の配管を含む補機を省
略でき、装置本体の小型化とともにシステムのコンパク
ト化も達成できる。Filling a layered space separated by partition walls with a reforming catalyst to form a reforming catalyst layer, and similarly configuring the heating section of this reforming catalyst layer with a layered flow path space, these are: They can be stacked to form one reformer. Moreover, by alternately arranging and stacking the reforming catalyst layer, which serves as a heat receiving body, and the heating section, the heat from the heat generating section can be effectively transferred to the reforming catalyst layer, which is the reaction section, without heat loss to the outside. can. In addition, the stacked structure does not have any surplus space like a reaction tube type device, so even if the number of stacked layers is increased and the processing capacity of the device is increased, the surplus space will not increase, and the minimum necessary size will always be maintained. drooping Further, to the reformer having such a laminated structure, a heat recovery section equivalent to a plate heat exchanger can be easily added without impairing the function of the reformer main body. This heat recovery section is
As with the formation of each catalyst layer, flow channels separated by partition walls are simply provided in the reformer body, and the structure of the reformer remains essentially the same. High-temperature combustion exhaust gas or reformed gas generated by the device itself can be flowed in as a heat source, and the reformed raw material or combustion air can be used as a low heat source for heat recovery. Conventionally, such heat recovery was performed using a heat exchanger installed outside the reformer, but in the reformer with this structure, these functions are satisfied only by the equipment itself, so the reformer itself is not required. Auxiliary equipment including surrounding piping can be omitted, making it possible to downsize the device body and the system.
以下、本発明の一実施例を第1図により説明する。 An embodiment of the present invention will be described below with reference to FIG.
第1図は本発明による燃料改質装置の実施例を断面図で
示したものである。本実施例は、改質触媒層三段、加熱
層四段で構成される改質装置本体の両側に各々一段のガ
ス流路を設けた場合の構成からなる燃料改質装置を例示
したものである。本実施例はメタンを原料とする改質装
置として用いられるが、改質触媒4を変えることで、ア
ルコール類の改質にも適用できるので、メタンの改質に
限定したものではない。FIG. 1 shows a cross-sectional view of an embodiment of a fuel reformer according to the present invention. This example illustrates a fuel reformer that has a structure in which one stage of gas flow passages is provided on each side of the reformer main body, which is composed of three stages of reforming catalyst layers and four stages of heating layers. be. Although this embodiment is used as a reformer using methane as a raw material, it is not limited to reforming methane because it can also be applied to reforming alcohols by changing the reforming catalyst 4.
以下1本実施例の機能を述べる。改質原料1は、メタン
と水蒸気を混合したものであり1通常、この比はスチー
ムカーボン比(S/C)として2.5 ないし4.5
の値を用いる。この改質原料は、初めに装置の両側に設
けたガス流路6に導かれる。この流路では、加熱層が片
側に隣接しているため、ここから熱を受はガス流路に導
かれた原料は予熱される。この流路を出た改質原料は、
集合管12で両側から集められ、続いて各改質触媒層に
分配供給される、改質触媒層にはメタン改質用に、ニッ
ケル系の改質触媒4が充填されている。改質原料は、こ
の改質触媒層で反応し、水素リッチな改質ガス9になる
。このときの反応温度は約800℃の平衡温度になるよ
うに隣接する加熱部から熱が与えられる。本実施例の加
熱部は第1図(a)に示す構造になっている。すなわち
、加熱層にはパラジウム系の燃焼触媒3が充填されてお
り、さらに、燃焼触媒層中に燃料供給管7が三本挿入さ
れている。燃料供給管は、異常燃焼により局部的に高温
にならないように、燃焼触媒層への燃料を均一に分散す
るため、多数のノズル孔があけられている。この加熱部
構造により、ここに供給される予混合燃料2は触媒燃焼
により発熱し、改質触媒層へ熱を供給する。ここでの燃
焼は、燃焼触媒層の流路方向に沿って、三段からなる多
段燃焼が行なわれる。このため、燃焼触媒層は、流路方
向に沿った温度降下が無い等温度熱面を維持できる。な
お、予混合燃料はメタンと空気の混合燃料であるが、燃
料電池システムにおける燃料水素を含むアノード排ガス
とカソード排ガスの混合したものなどが使用される場合
がある。燃焼加熱を終了した燃焼排ガス8は、下方の排
気管から排出される。これら、改質装置としての機能を
満足させるための構造は、図に示すように薄い耐熱材料
からなる隔壁5をケーシング14ではさみつけ、これら
全体を外壁と固定用ボルトで支持する構造を採用してい
る。また、外壁やケーシングを高温から守るため、それ
ぞれの内部には断熱材で内張すしている。本実施例では
、余剰空間の無い小型改質装置としている。たとえば、
燃料電池100 kW級に使用する燃料改質装置を設計
すると高さ1.5 m幅0.9m程度の大きさの装置に
なる。これは、従来の反応管型装置に比較すると、容積
にして、およそ115になる。さらに、装置の両側に設
けたガス流路は、低温の改質原料を流すため、高温の加
熱部の熱の遮へい効果もあり、外壁−の断熱層を薄くで
きる。The functions of this embodiment will be described below. The reforming raw material 1 is a mixture of methane and steam, and this ratio is normally 2.5 to 4.5 as a steam carbon ratio (S/C).
Use the value of This reformed raw material is first led to gas channels 6 provided on both sides of the device. In this flow path, since the heating layer is adjacent to one side, the raw material guided to the gas flow path is preheated by receiving heat from the heating layer. The reformed raw material leaving this flow path is
The reforming catalyst bed, which is collected from both sides by the collecting pipe 12 and then distributed and supplied to each reforming catalyst bed, is filled with a nickel-based reforming catalyst 4 for methane reforming. The reformed raw material reacts in this reforming catalyst layer and becomes hydrogen-rich reformed gas 9. Heat is applied from an adjacent heating section so that the reaction temperature at this time is an equilibrium temperature of about 800°C. The heating section of this embodiment has a structure shown in FIG. 1(a). That is, the heating layer is filled with a palladium-based combustion catalyst 3, and three fuel supply pipes 7 are inserted into the combustion catalyst layer. The fuel supply pipe is provided with a large number of nozzle holes in order to uniformly disperse the fuel to the combustion catalyst layer to prevent localized high temperatures due to abnormal combustion. With this heating section structure, the premixed fuel 2 supplied here generates heat through catalytic combustion, and supplies heat to the reforming catalyst layer. The combustion here is a multi-stage combustion consisting of three stages along the flow path direction of the combustion catalyst layer. Therefore, the combustion catalyst layer can maintain an isothermal heat surface with no temperature drop along the flow path direction. Note that the premixed fuel is a mixed fuel of methane and air, but a mixture of anode exhaust gas and cathode exhaust gas containing fuel hydrogen in a fuel cell system may be used. The combustion exhaust gas 8 that has been heated by combustion is discharged from the lower exhaust pipe. As shown in the figure, the structure to satisfy the function of the reformer is such that a partition wall 5 made of a thin heat-resistant material is sandwiched between a casing 14 and the entire structure is supported by an outer wall and fixing bolts. ing. In addition, to protect the outer walls and casing from high temperatures, the inside of each is lined with insulation material. In this embodiment, a small-sized reformer with no surplus space is used. for example,
When designing a fuel reformer for use in a 100 kW class fuel cell, it would be approximately 1.5 m high and 0.9 m wide. This is approximately 115 in volume compared to a conventional reaction tube type device. Furthermore, since the gas channels provided on both sides of the device allow low-temperature reforming raw materials to flow, they also have the effect of shielding the heat from the high-temperature heating section, allowing the insulation layer on the outer wall to be made thinner.
第3図は、改質装置両側に設けるガス流路の段数をさら
に増やし、改質原料の予熱に改質ガスの顕熱をも回収し
て用いるようにした一実施例を示したものである。この
隔壁構造と流路構成により。Figure 3 shows an embodiment in which the number of stages of gas flow paths provided on both sides of the reformer is further increased, and the sensible heat of the reformed gas is also recovered and used for preheating the reformed raw material. . Due to this partition wall structure and flow path configuration.
改質装置から排出される改質ガス温度を降下させ、燃料
電池と組み合わせる燃料改質システムを考えると、次の
プロセスであるシフト反応に適する温度にすることがで
きる。すなわち、従来、第5図に示すように、シフトコ
ンバータと燃料改質装置の間には、改質ガスの温度を下
げるための熱交換器が設けられていた。しかし、本実施
例の構造では、これらの熱交換器は不用になる。If we consider a fuel reforming system that lowers the temperature of the reformed gas discharged from the reformer and combines it with a fuel cell, it is possible to bring it to a temperature suitable for the next process, the shift reaction. That is, conventionally, as shown in FIG. 5, a heat exchanger was provided between the shift converter and the fuel reformer to lower the temperature of the reformed gas. However, in the structure of this embodiment, these heat exchangers are unnecessary.
第4図は、改質装置両側のガス流路を各々三段にして熱
の有効利用を図る流路構成にした実施例を示す、これは
、温度の低い改質原料を一番外側のガス流路から通過す
るようにしたものであり。Figure 4 shows an example in which the gas flow paths on both sides of the reformer are arranged in three stages to achieve effective heat utilization. It is designed to pass through the flow path.
外壁に対する効果は第1図の実施例と同様となる。The effect on the outer wall is similar to that of the embodiment shown in FIG.
第6図は、ガス流路を両側に各々四段設けた場合の流路
構成を示す。これは、燃焼ガスの頭熱も熱回収に利用す
るものであり、第5図に示す燃料電池システムにおいて
、燃料改質装置周りの三個の熱交換器を一体化した改質
装置に相当する。この場合の流路構成は、隣接する流路
を通過するガスは各々温度差の大きいものを選択してい
る。このため、各流路間の熱移動が効果的に行われる。FIG. 6 shows a flow path configuration in which four stages of gas flow paths are provided on each side. This uses the head heat of the combustion gas for heat recovery, and corresponds to a reformer that integrates three heat exchangers around the fuel reformer in the fuel cell system shown in Figure 5. . In this case, the flow path configuration is such that gases passing through adjacent flow paths each have a large temperature difference. Therefore, heat transfer between each flow path is effectively performed.
また、本実施例のように、ガス流路の段数を増してくる
とこれらの流路は、改質装置自身の熱の授受だけでなく
他の機器で発生するガスの熱交換器としての利用もでき
る。例えば、第6図の実施例における供給空気は、燃料
電池で排出されるカソード徘空気22を用いることもで
きる。In addition, as in this example, when the number of stages of gas flow paths is increased, these flow paths are used not only for receiving and receiving heat from the reformer itself, but also as a heat exchanger for gas generated by other equipment. You can also do it. For example, the supply air in the embodiment of FIG. 6 may be the cathode wandering air 22 discharged from the fuel cell.
第7図は、改質触媒層及び加熱層の@層数が大きくなっ
た場合の熱回収の構造の一実施例を示す。FIG. 7 shows an example of a heat recovery structure when the number of reforming catalyst layers and heating layers is increased.
すなわち、改質装置内部で発生するガス厘が多くなると
装置の両側に設けたガス流路だけではこれらの機能を果
たすことが困難になる。この場合、各触媒層毎に自己熱
回収するようにしたものが本実施例である。これは、従
来の反応管型の熱回収法と構造的に近いが本実施例では
平面の積層型であるため装置が大容量になるほど小型化
に対するメリットが大きくなる。That is, when the amount of gas generated inside the reformer increases, it becomes difficult to perform these functions using only the gas channels provided on both sides of the reformer. In this case, in this embodiment, self-heat recovery is performed for each catalyst layer. This is similar in structure to the conventional reaction tube type heat recovery method, but since this embodiment uses a planar stacked type, the larger the capacity of the device, the greater the advantage in terms of miniaturization.
本発明によれば、装置の構成に無駄な余剰空間が発生せ
ず、改質装置の小型化に対して効果がある。また、改質
装置で発生する改質ガスや燃焼排ガスの熱回収を容易に
行うことができる。According to the present invention, unnecessary surplus space is not generated in the configuration of the device, and it is effective in downsizing the reforming device. Further, heat recovery from the reformed gas and combustion exhaust gas generated in the reformer can be easily performed.
第1図は本発明の一実施例の断面図、第2図は従来型改
質装置の断面図、第3図は本発明の一実施例の流路断面
図、第4図は本発明の一実施例の流路断面図、第5図は
燃料電池システム例を示すフローチャート、第6図は本
発明の一実施例の流路断面図、第7図は本発明の一実施
例の断面図である。
1・・・改質原料、2・・・予混合燃料、3・・・燃焼
触媒、4・・・改質触媒。Fig. 1 is a sectional view of an embodiment of the present invention, Fig. 2 is a sectional view of a conventional reformer, Fig. 3 is a flow path sectional view of an embodiment of the invention, and Fig. 4 is a sectional view of a conventional reformer. FIG. 5 is a flowchart showing an example of a fuel cell system; FIG. 6 is a cross-sectional view of a flow path according to an embodiment of the present invention; FIG. 7 is a cross-sectional view of an embodiment of the present invention. It is. 1... Reforming raw material, 2... Premixed fuel, 3... Combustion catalyst, 4... Reforming catalyst.
Claims (1)
質により水素リッチガスを生成するため、前記改質原料
を供給し反応させる改質触媒を充填して前記改質触媒層
とした改質部と、前記改質触媒層に熱を与えるため、高
温燃焼ガスを導入、あるいは、発生させる加熱部から構
成される燃料改質装置において、 前記改質部と前記加熱部は各々隔壁で区切られた層状空
間の積層体から成り、前記層状空間の両側に前記加熱部
が位置するようにして、前記加熱部と前記改質部を交互
に配置し、さらに、両側の前記加熱部の外側に隣接して
各々隔壁で区切られた層状のガス流路を設けたことを特
徴とする燃料改質装置。 2、特許請求の範囲第1項の燃料改質装置において、前
記加熱部を酸化触媒を充填した燃焼触媒層とし、前記燃
焼触媒層には、複数の燃料供給管を流路方向に配置し、
前記加熱部で多段燃焼させることを特徴とする燃料改質
装置。 3、特許請求の範囲第1項または第2項の燃料改質装置
において、 前記ガス流路を各々一段設け、前記改質原料が前記ガス
流路を通過した後に前記改質部へ供給される流路構造と
したことを特徴とする燃料改質装置。 4、特許請求の範囲第1項または第2項の燃料改質装置
において、 前記ガス流路を各々二段設け、内側の前記ガス流路には
前記改質触媒層に供給する前の改質原料を導き、外側の
前記ガス流路には、前記改質部で生成した、改質ガスを
導く流路構造にしたことを特徴とする燃料改質装置。 5、特許請求の範囲第1項または第2項の燃料改質装置
において、 前記ガス流路を各々三段設け、前記改質原料を初めに外
側の前記ガス流路に導入し、次に内側の前記ガス流路に
導き、これらを通過したあとに前記改質触媒層に供給す
るようにし、中間の前記ガス流路には、前記改質触媒層
で生成した改質ガスを導くような流路構造にしたことを
特徴とする燃料改質装置。 6、特許請求の範囲第1項または第2項の燃料改質装置
において、前記ガス流路を各々四段設け、改質原料は、
内側の前記ガス流路を通過したあとに前記改質触媒層に
供給され、ここで生成した改質ガスは外側の前記ガス流
路に導かれここを通過したあと系外へ排出され、また、
前記加熱部に送る燃焼用空気を外側から二段目の前記ガ
ス流路を通過したあと燃料と予混合させ、前記加熱部を
出た排出ガスを内側から2段目の前記ガス流路に導く流
路構造としたことを特徴とする燃料改質装置。 7、特許請求の範囲第1項または第2項の燃料改質装置
において、各々の前記改質触媒層内に二枚の隔壁で作る
改質ガスの戻り流路を設けたことを特徴とする燃料改質
装置。 8、特許請求の範囲第1項ないし第7項の燃料改質装置
において、前記ガス流路を構成する前記隔壁に、板状な
いしピン状の突起からなる伝熱フィンを設けたことを特
徴とする燃料改質装置。 9、特許請求の範囲第1項ないし第7項の燃料改質装置
において、前記ガス流路に金属またはセラミック製の粒
子を充填したことを特徴とする燃料改質装置。[Scope of Claims] 1. Hydrocarbons and alcohols are used as reforming raw materials, and in order to generate hydrogen-rich gas through steam reforming, the reforming catalyst is filled with a reforming catalyst for supplying and reacting the reforming raw materials. In a fuel reformer comprising a layered reforming section and a heating section that introduces or generates high-temperature combustion gas in order to give heat to the reforming catalyst layer, the reforming section and the heating section are It consists of a laminate of layered spaces each separated by partition walls, and the heating portions and the reforming portions are arranged alternately so that the heating portions are located on both sides of the layered spaces, and the heating portions on both sides are arranged alternately. 1. A fuel reforming device characterized in that layered gas flow paths each separated by a partition wall are provided adjacent to the outside of the fuel reformer. 2. In the fuel reformer according to claim 1, the heating section is a combustion catalyst layer filled with an oxidation catalyst, and the combustion catalyst layer has a plurality of fuel supply pipes arranged in the flow path direction,
A fuel reformer characterized in that the heating section performs multistage combustion. 3. In the fuel reformer according to claim 1 or 2, each of the gas passages is provided in one stage, and the reforming raw material is supplied to the reforming section after passing through the gas passages. A fuel reformer characterized by having a flow path structure. 4. In the fuel reformer according to claim 1 or 2, each of the gas flow paths is provided in two stages, and the inner gas flow path contains a reforming gas before being supplied to the reforming catalyst layer. A fuel reforming device characterized in that a raw material is guided, and the outer gas flow channel has a flow channel structure that guides reformed gas generated in the reforming section. 5. In the fuel reformer according to claim 1 or 2, each of the gas flow channels is provided in three stages, and the reforming raw material is first introduced into the outer gas flow channel, and then into the inner gas flow channel. The intermediate gas flow path includes a flow that guides the reformed gas generated in the reforming catalyst layer. A fuel reformer characterized by having a road structure. 6. In the fuel reformer according to claim 1 or 2, each of the gas flow paths is provided in four stages, and the reforming raw material is
After passing through the gas flow path on the inside, the reformed gas is supplied to the reforming catalyst layer, and the reformed gas generated here is led to the gas flow path on the outside, passes through it, and is then discharged to the outside of the system.
Combustion air to be sent to the heating section passes through the gas flow path in the second stage from the outside and is then premixed with fuel, and the exhaust gas exiting the heating section is guided to the gas flow path in the second stage from the inside. A fuel reformer characterized by having a flow path structure. 7. The fuel reformer according to claim 1 or 2, characterized in that a reformed gas return passage formed by two partition walls is provided in each of the reforming catalyst layers. Fuel reformer. 8. The fuel reformer according to claims 1 to 7, characterized in that the partition wall constituting the gas flow path is provided with heat transfer fins consisting of plate-like or pin-like projections. fuel reformer. 9. A fuel reformer according to any one of claims 1 to 7, characterized in that the gas flow path is filled with metal or ceramic particles.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62125894A JPS63291802A (en) | 1987-05-25 | 1987-05-25 | Fuel reforming apparatus |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62125894A JPS63291802A (en) | 1987-05-25 | 1987-05-25 | Fuel reforming apparatus |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS63291802A true JPS63291802A (en) | 1988-11-29 |
Family
ID=14921541
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP62125894A Pending JPS63291802A (en) | 1987-05-25 | 1987-05-25 | Fuel reforming apparatus |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS63291802A (en) |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0364865A (en) * | 1989-07-31 | 1991-03-20 | Ishikawajima Harima Heavy Ind Co Ltd | Molten carbonate fuel cell power generation device |
| US5180561A (en) * | 1989-11-27 | 1993-01-19 | Ishikawajima-Harima Heavy Industries Co., Ltd. | Plate type reformer assembly |
| US5270127A (en) * | 1991-08-09 | 1993-12-14 | Ishikawajima-Harima Heavy Industries Co., Ltd. | Plate shift converter |
| US5316747A (en) * | 1992-10-09 | 1994-05-31 | Ballard Power Systems Inc. | Method and apparatus for the selective oxidation of carbon monoxide in a hydrogen-containing gas mixture |
| EP0691701A1 (en) * | 1994-07-05 | 1996-01-10 | Ishikawajima-Harima Heavy Industries Co., Ltd. | Plate reformer |
| WO1997024176A1 (en) * | 1995-12-27 | 1997-07-10 | International Fuel Cell Corporation | Compact hydrocarbon fuel gas reformer assemblage |
| JP2004503067A (en) * | 2000-07-10 | 2004-01-29 | グローバル サーモエレクトリック インコーポレイテッド | Integrated module for solid oxide fuel cell system |
| JP2010069355A (en) * | 2008-09-16 | 2010-04-02 | Mitsubishi Chemicals Corp | Plate type reactor and method for manufacturing reaction product using the same |
| JP2011251858A (en) * | 2010-05-31 | 2011-12-15 | Japan Petroleum Energy Center | Heat exchange type organic hydride dehydrogenation system |
-
1987
- 1987-05-25 JP JP62125894A patent/JPS63291802A/en active Pending
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0364865A (en) * | 1989-07-31 | 1991-03-20 | Ishikawajima Harima Heavy Ind Co Ltd | Molten carbonate fuel cell power generation device |
| US5180561A (en) * | 1989-11-27 | 1993-01-19 | Ishikawajima-Harima Heavy Industries Co., Ltd. | Plate type reformer assembly |
| US5270127A (en) * | 1991-08-09 | 1993-12-14 | Ishikawajima-Harima Heavy Industries Co., Ltd. | Plate shift converter |
| US5316747A (en) * | 1992-10-09 | 1994-05-31 | Ballard Power Systems Inc. | Method and apparatus for the selective oxidation of carbon monoxide in a hydrogen-containing gas mixture |
| US5456889A (en) * | 1992-10-09 | 1995-10-10 | Her Majesty The Queen In Right Of Canada, As Represented By The Minister Of National Defence | Apparatus for the selective oxidation of carbon monoxide in a hydrogen-containing gas mixture |
| EP0691701A1 (en) * | 1994-07-05 | 1996-01-10 | Ishikawajima-Harima Heavy Industries Co., Ltd. | Plate reformer |
| US5609834A (en) * | 1994-07-05 | 1997-03-11 | Ishikawajima-Harima Heavy Industries Co., Ltd. | Plate reformer |
| US5670269A (en) * | 1994-07-05 | 1997-09-23 | Ishikawajima-Harima Heavy Industries, Co., Ltd. | Molten carbonate power generation system with plate reformer |
| WO1997024176A1 (en) * | 1995-12-27 | 1997-07-10 | International Fuel Cell Corporation | Compact hydrocarbon fuel gas reformer assemblage |
| JP2004503067A (en) * | 2000-07-10 | 2004-01-29 | グローバル サーモエレクトリック インコーポレイテッド | Integrated module for solid oxide fuel cell system |
| JP2010069355A (en) * | 2008-09-16 | 2010-04-02 | Mitsubishi Chemicals Corp | Plate type reactor and method for manufacturing reaction product using the same |
| JP2011251858A (en) * | 2010-05-31 | 2011-12-15 | Japan Petroleum Energy Center | Heat exchange type organic hydride dehydrogenation system |
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