JPS61114730A - Catalytic reaction apparatus - Google Patents

Catalytic reaction apparatus

Info

Publication number
JPS61114730A
JPS61114730A JP59234960A JP23496084A JPS61114730A JP S61114730 A JPS61114730 A JP S61114730A JP 59234960 A JP59234960 A JP 59234960A JP 23496084 A JP23496084 A JP 23496084A JP S61114730 A JPS61114730 A JP S61114730A
Authority
JP
Japan
Prior art keywords
catalyst
inner cylinder
cylinder
support
outer cylinder
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
Application number
JP59234960A
Other languages
Japanese (ja)
Other versions
JPH0365228B2 (en
Inventor
Yoshiaki Amano
天野 義明
Eiji Yokoyama
英二 横山
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.)
Hitachi Ltd
Original Assignee
Hitachi 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 Hitachi Ltd filed Critical Hitachi Ltd
Priority to JP59234960A priority Critical patent/JPS61114730A/en
Publication of JPS61114730A publication Critical patent/JPS61114730A/en
Publication of JPH0365228B2 publication Critical patent/JPH0365228B2/ja
Granted 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
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/02Chemical 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
    • B01J8/06Chemical 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 in tube reactors; the solid particles being arranged in tubes
    • 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

Abstract

PURPOSE:To suppress the expansion and contraction of a reaction tube caused by the heat of catalytic reaction, by constituting a catalyst holding means from a tray part, a first support for holding the tray part by an outer cylinder and a second support for holding said tray part by an inner cylinder. CONSTITUTION:Reaction gas 9 comprising a mixture of natural gas and steam is guided to a space part packed with a catalyst 3 and heated herein by a burner 7 to generate steam reforming reaction. The formed gas containing a large amount of hydrogen passes along the inner peripheral surface of an inner cylinder 2 to be sent out to the outside of a shell 8 as gas 10. The inner cylinder 2 is thermally expanded after an outer cylinder 1 was thermally expanded but, because the inner cylinder 2 is extended to the longitudinal direction, a mesh tray is supported by a second support 13 and the compression of the catalyst 3 due to the reduction of a gap 4 can be suppressed. Thereafter, the apparatus enters a steady and the mesh tray 5 is supported by first and second supports 12, 13.

Description

【発明の詳細な説明】 本発明は、触媒反応装置に係り、特に、触媒を封入した
反応管の熱膨張,熱収縮に起因する触媒の破壊を防止す
る触媒反応装置に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a catalytic reaction apparatus, and more particularly to a catalytic reaction apparatus that prevents destruction of a catalyst due to thermal expansion and contraction of a reaction tube in which a catalyst is enclosed.

〔発明の背景〕[Background of the invention]

外筒,内筒を具え、外筒の内周面と内筒の外周面とで構
成された空間部に触媒を封入した反応部に、加熱しなが
ら反応ガスを通し、化学反応を起させる装置の一例とし
て燃料電池装置のリフオーマがある,このリフオーマは
、天然ガスと水蒸気の混合ガスを上記空間部に導き、こ
こでバーナにより外部から加熱しながら水素を多量に含
むガスとするものである。
A device that is equipped with an outer cylinder and an inner cylinder, and causes a chemical reaction by passing a reaction gas while heating it through a reaction section in which a catalyst is sealed in a space formed by the inner peripheral surface of the outer cylinder and the outer peripheral surface of the inner cylinder. An example of this is a re-former for a fuel cell device. This re-former introduces a mixed gas of natural gas and water vapor into the above-mentioned space, where it is heated from the outside by a burner to form a gas containing a large amount of hydrogen.

このように構成されたリフオーマにおいては。In the refoma configured in this way.

外筒と内筒の間の空間部の径方向の寸法(以後ギャップ
と呼ぶ)は装置の立上げ時(運転開始時)と立下げ時(
停止時)では、熱膨張によってその大きさが異なる。従
って、ギャップが拡大する際には、空間部に配置された
触媒の粒子はギャップの拡大によって生じた隙間を埋め
るようにその自重によって落ちて来る。逆に、ギャップ
が収縮する際は、触媒の粒子は上方に押し上げられるが
、このとき触媒には圧縮力や摩擦力のような触媒を破壊
しようとする力が働くため、装置が起動、停止を繰り返
すうちに、触媒が破壊されている。
The radial dimension of the space between the outer cylinder and the inner cylinder (hereinafter referred to as the gap) is determined at the time of startup (starting operation) and the time of shutdown (
(when stopped), its size differs depending on thermal expansion. Therefore, when the gap widens, the catalyst particles placed in the space fall under their own weight to fill the gap created by the widening of the gap. Conversely, when the gap contracts, the catalyst particles are pushed upwards, but at this time, forces that try to destroy the catalyst, such as compressive force and frictional force, act on the catalyst, making it difficult for the equipment to start or stop. As the process is repeated, the catalyst is destroyed.

この現象については、Gas Re5earch In
5tituteによるOn 5ite Fuel Ce
1l Power PlantTechnology 
 and  DeveLopnent、Progra+
w、AnualReport (Jan 1982−J
an 1983)において「スランピング」と呼び論じ
られている。
This phenomenon is explained in Gas Research In
On 5ite Fuel Ce by 5tiute
1l Power Plant Technology
and DevLopnent, Progra+
w, Annual Report (Jan 1982-J
1983), it is called ``slumping'' and discussed.

しかしながら、このスランピングを防止するための方法
として外筒と内筒の間の空間部の長手方向に単に触媒を
支えるための複数の棚を設けることが提案されているが
、この方法は、上記起動。
However, as a method to prevent this slumping, it has been proposed to simply provide a plurality of shelves in the longitudinal direction of the space between the outer cylinder and the inner cylinder to support the catalyst. .

停止にもとづく触媒の移動を本質的に防止するものでは
なく、触媒の破壊を本質的に防止するものではない。
It does not inherently prevent catalyst migration due to shutdown, nor does it inherently prevent catalyst destruction.

ちなみに、内径が100m+i、長さが1600mm(
7)外筒、内径が30mm、長さが1500mmの内筒
の熱膨張の一例を具体的に示すと、外筒の径方向で0 
、36m+o 。
By the way, the inner diameter is 100m+i and the length is 1600mm (
7) To specifically show an example of thermal expansion of an inner cylinder with an inner diameter of 30 mm and a length of 1500 mm, the thermal expansion is 0 in the radial direction of the outer cylinder.
, 36m+o.

長手方向で、18mmの熱膨張、また、内筒の径方向で
1.2 mm、長手方向で191!III+の熱膨張を
有する。
Thermal expansion is 18 mm in the longitudinal direction, 1.2 mm in the radial direction of the inner cylinder, and 191 mm in the longitudinal direction! It has a thermal expansion of III+.

〔発明の目的〕[Purpose of the invention]

本発明の目的は、触媒の反応熱によって生じる反応管の
拡大、収縮に起因する触媒の破壊を抑制する手段を提供
することにある。
An object of the present invention is to provide a means for suppressing destruction of a catalyst caused by expansion and contraction of a reaction tube caused by reaction heat of the catalyst.

〔発明の概要〕[Summary of the invention]

上記目的を達成するために、本発明は、触媒保持手段の
支持を触媒反応装置の立上げ時と立下げ時で変えるよう
に構成したものである。このように構成することによっ
て、触媒に加えられる圧縮力や摩擦力を軽減し、触媒の
破壊を抑制できる6〔発明の実施例〕 以下、本発明の一実施例を第1図ないし第5図にもとづ
き、説明する。
In order to achieve the above object, the present invention is configured such that the support of the catalyst holding means is changed when the catalytic reaction apparatus is started up and when it is stopped down. With this configuration, the compressive force and frictional force applied to the catalyst can be reduced, and the destruction of the catalyst can be suppressed.6 [Embodiment of the Invention] Hereinafter, an embodiment of the present invention is shown in Figs. 1 to 5. I will explain based on this.

第1図、第2図は、触媒反応装置の一例として燃料電池
装置のリフオーマを掲げて示したもので、同図に示す如
く、リフオーマは、内筒2、内筒2と同心的に配置され
た外筒1、内@2の外周面と外筒1の内周面とで形成さ
れる環状部、すなわち空間部に封入された触媒3とから
構成される反応部H8〜H7と、これらを包囲するよう
に配置したシェル6と、反応部H1ないしH7を加熱す
るバーナ7、とを主要部とする。そして、内筒2、外筒
1の断面は円形状に形成されていると共に外筒1の一端
は、開口し、他端は閉塞し、内筒2の一端は反応ガス9
を導出する管路11に連結し、他端を外筒1の閉塞端近
傍に開口している。また、反応部H,ないしH7は、シ
ェル6内に並設するよう構成され、管路11はシェル6
内において、各反応部の内WIJ2の一端を集合するよ
うに構成している。8はシェル6の断熱材である。
FIG. 1 and FIG. 2 show a rifohmer of a fuel cell device as an example of a catalytic reaction device. As shown in the figure, the refohmer is arranged concentrically with the inner cylinder 2 and the inner cylinder 2. The reaction parts H8 to H7 are composed of an annular part formed by the outer peripheral surface of the outer cylinder 1 and inner @2 and the inner peripheral surface of the outer cylinder 1, that is, the catalyst 3 sealed in the space; The main parts are a shell 6 arranged to surround it and a burner 7 that heats the reaction sections H1 to H7. The inner tube 2 and the outer tube 1 have circular cross sections, one end of the outer tube 1 is open and the other end is closed, and one end of the inner tube 2 is open to the reaction gas 9.
The other end is opened near the closed end of the outer cylinder 1. Further, the reaction parts H, to H7 are arranged in parallel in the shell 6, and the pipe line 11 is arranged in the shell 6.
Inside, one end of the WIJ2 of each reaction section is assembled. 8 is a heat insulating material of the shell 6.

更に、第1図において、5は、外筒1.内筒2の下端で
触媒3を保持する目皿で、第3図に詳細を示したような
支持体で支持される。第3図に示すように、目皿5は内
筒2の外周面と外筒1の内周面とで形成される空間部に
適合するように環状に形成されている。12.13は、
目皿5を外筒1、内筒2の下端部で支持する第1.第2
の支持体で、それぞれ環状に形成されている。そしで、
第1の支持体12の外周面ば外筒1の内周面に、第2の
支持体13の内周面ば内筒2の外周面に固着されている
。また、第1.第2の支持体1,2の目皿5の下面に対
向するそれぞれの面積は、目皿5をそれぞれ単独に移動
できる広さに構成されている。目皿5を第1.第2の支
持体12.13により支持する理由は、次の通りである
Furthermore, in FIG. 1, 5 indicates the outer cylinder 1. A perforated plate that holds the catalyst 3 at the lower end of the inner cylinder 2 is supported by a support as shown in detail in FIG. As shown in FIG. 3, the perforated plate 5 is formed into an annular shape so as to fit into the space formed by the outer circumferential surface of the inner tube 2 and the inner circumferential surface of the outer tube 1. As shown in FIG. 12.13 is
The first plate supports the perforated plate 5 at the lower ends of the outer cylinder 1 and the inner cylinder 2. Second
The supports are each shaped like a ring. Then,
The outer circumferential surface of the first support body 12 is fixed to the inner circumferential surface of the outer tube 1 , and the inner circumferential surface of the second support body 13 is fixed to the outer circumferential surface of the inner tube 2 . Also, 1st. The area of each of the second supports 1 and 2 facing the lower surface of the perforated plate 5 is configured to be large enough to allow the perforated plate 5 to be moved independently. Place the perforated plate 5 in the first position. The reason for supporting by the second support body 12.13 is as follows.

リフオーマの立上げ時は、外筒1が熱膨張した後、内筒
2が熱膨張する。従って、この場合、第2の支持体13
で目皿5を支持すれば、触媒3の圧縮破壊が防止できる
。この理由は、たとえば上記とは逆に、第1の支持体1
2で支持するように構成すると(第2の支持体13が存
在しないということになる)、外筒lが径方向、長手方
向に伸びると触媒3がその体積増加分だけ自重で下りで
くる。しかる後、内筒2が膨張すると、上記自重で下り
てきた触媒3の逃げ場がなくなって(触媒3を上昇させ
るしかない)、触媒3の圧縮破壊が生じやすい状態にな
る。
When starting up the re-former, the outer cylinder 1 thermally expands, and then the inner cylinder 2 thermally expands. Therefore, in this case, the second support 13
By supporting the perforated plate 5, compression destruction of the catalyst 3 can be prevented. The reason for this is that, for example, contrary to the above, the first support 1
2 (this means that the second support body 13 does not exist), when the outer cylinder 1 extends in the radial and longitudinal directions, the catalyst 3 will descend by its own weight by the volume increase. After that, when the inner cylinder 2 expands, there is no place for the catalyst 3, which has descended under its own weight, to escape (there is no choice but to raise the catalyst 3), and the catalyst 3 becomes susceptible to compression failure.

二元に対して、第2の支持体13で目皿5を支持すれば
、内筒2の膨張にともなって第2の支持体13も長手方
向へ移動するので、体積増加がはかられる。従って、上
記自重で下りてきた触媒を圧縮させることがおこらない
In contrast to the binary structure, if the perforated plate 5 is supported by the second support 13, the second support 13 also moves in the longitudinal direction as the inner cylinder 2 expands, so that the volume can be increased. Therefore, the catalyst that has come down due to its own weight is not compressed.

また、リフオーマの立下げ時は、外筒1が先にこの摩擦
エネルギーが触媒3の破壊・変形に消費されると考えら
れるので、この場合は摩擦面積が小さい方が良いので、
目皿5は第1の支持体12で支持される。
In addition, when the re-former is brought down, the frictional energy of the outer cylinder 1 is likely to be consumed first in destroying and deforming the catalyst 3, so in this case, it is better to have a smaller frictional area.
The perforated plate 5 is supported by a first support 12.

第1図に戻って、上記のように構成されたリフオーマに
おいて、天然ガスと水蒸気の混合した反応ガス9は、触
媒3を封入した空間部に導かれ、ここで、バーナ7によ
り加熱されながら水蒸気改質反応を起こし、水素を多量
に含むガスとなり、内筒2の内周面を通過し、ガス10
としてシェル8外へ送出される。尚、第1図ないし第3
図中において、4は外筒1と内筒2の間の空間部の径方
向の寸法すなわち、ギャップである。
Returning to FIG. 1, in the re-former configured as described above, the reaction gas 9, which is a mixture of natural gas and water vapor, is guided into a space in which a catalyst 3 is enclosed, where it is heated by a burner 7 and steamed into water. A reforming reaction occurs, resulting in a gas containing a large amount of hydrogen, which passes through the inner peripheral surface of the inner cylinder 2 and becomes gas 10.
It is sent out to the outside of the shell 8 as a. In addition, Figures 1 to 3
In the figure, 4 is the radial dimension of the space between the outer cylinder 1 and the inner cylinder 2, that is, the gap.

次に、上記の通り構成された一実施例の作用について第
5図にもとづいて説明する。第5図において、(A)は
触媒反応装置、すなわちリフオーマの停止時の一つの反
応部の状態を説明する図、以下同じく(B)は立上げ時
、(C)は定常運転時、(D)は立下げ時、(E)は停
止時の状態を説明する図である。なお、第5図において
、第1図ないし第4図と同一物には符号を付しである。
Next, the operation of the embodiment configured as described above will be explained based on FIG. 5. In FIG. 5, (A) is a diagram explaining the state of one reaction section of the catalytic reaction apparatus, that is, when the re-former is stopped, (B) is the diagram at startup, (C) is the diagram during steady operation, and (D ) is a diagram illustrating the state at the time of falling, and (E) is a diagram explaining the state at the time of stopping. In FIG. 5, the same parts as those in FIGS. 1 to 4 are designated by reference numerals.

まず、第5図(A)の状態において、目皿5は第1.第
2の支持体12.13に支持されている。
First, in the state shown in FIG. 5(A), the perforated plate 5 is placed in the first position. It is supported on a second support 12.13.

次に、第5図(B)の状態について説明するにの状態に
おいては、外筒1が熱膨張した後に内1!I2が熱膨張
するが、内筒2が長手方向に伸びるため、第2の支持体
13により目皿5が支持される状態になり、ギャップ4
の減少による触媒3の圧縮を抑えることができる。その
後、装置は、定常状態になり、目皿5は第1.第2の支
持体12.13にて支持される(第5図(C)の状態)
Next, in the state shown in FIG. 5(B), after the outer cylinder 1 has thermally expanded, the inner cylinder 1! I2 thermally expands, but since the inner cylinder 2 extends in the longitudinal direction, the perforated plate 5 is supported by the second support 13, and the gap 4
It is possible to suppress compression of the catalyst 3 due to a decrease in . Thereafter, the device is in a steady state, and the perforated plate 5 is in the first position. Supported by the second support 12.13 (state shown in Figure 5(C))
.

次に、第5図(D)の状態について説明する。Next, the state shown in FIG. 5(D) will be explained.

この状態においては、外筒1が先に縮み、遅れて内筒2
が収縮するが、目皿5が第1の支持板12によって上方
に持ち上げられる。このとき、触媒3は外ftJI、内
筒2の管壁を摩擦しながら上昇していく。この摩擦エネ
ルギーは触媒の破壊、変形に消費されるものと考えられ
るが、この場合、触媒3が均一に詰まっているならば外
筒1および内筒2の管壁に加わる、触媒3の自重による
単位面積当りの力は、外筒1も内筒2も同じである。し
たがって、摩擦力Fは。
In this state, the outer cylinder 1 contracts first, and the inner cylinder 2 contracts later.
contracts, but the perforated plate 5 is lifted upward by the first support plate 12. At this time, the catalyst 3 rises while rubbing against the outer ftJI and the pipe wall of the inner cylinder 2. It is thought that this frictional energy is consumed in the destruction and deformation of the catalyst, but in this case, if the catalyst 3 is evenly packed, it is due to the own weight of the catalyst 3 that is applied to the pipe walls of the outer cylinder 1 and the inner cylinder 2. The force per unit area is the same for both the outer cylinder 1 and the inner cylinder 2. Therefore, the frictional force F is.

F=trPS(ここで、μ:触媒と管壁との摩擦係数、
P:単位面積当りの力(高さ方向平均)。
F=trPS (where, μ: coefficient of friction between the catalyst and the tube wall,
P: Force per unit area (average in height direction).

S:摩擦面積)で表わされるが、触媒3は内筒2の内壁
に沿うよう移動されるので、摩擦力が小さく、触媒3の
破壊が少なくなる。しかる後、装置が停止されると第5
図(E)の状態に移るが、この場合は、第5図(A)の
状態と同様に目皿5は第1.第2の支持体12.13に
て支持される。
S: Frictional area) Since the catalyst 3 is moved along the inner wall of the inner cylinder 2, the frictional force is small and the destruction of the catalyst 3 is reduced. After that, when the device is stopped, the fifth
The state moves to the state shown in FIG. It is supported on a second support 12.13.

尚、上記実施例では、外筒、内筒を断面円形状のもので
説明したが、本発明はこれに限定されることなく本発明
の精神を逸脱しない限りにおいて断面多角形のものまで
含むべきものであることはむろんである。
In the above embodiments, the outer cylinder and the inner cylinder have circular cross-sections, but the present invention is not limited to this, and may include polygonal cross-sections as long as they do not depart from the spirit of the invention. Of course it is a thing.

〔発明の効果〕〔Effect of the invention〕

本発明によれば、触媒に作用する圧縮力、!11擦力を
小さくすることができるので、触媒の破壊を小さくする
ことができる効果がある。
According to the invention, the compressive force acting on the catalyst, ! 11 Since the frictional force can be reduced, there is an effect that the destruction of the catalyst can be reduced.

このことは触媒の破壊による微細化に起因する反応ガス
の圧力損失増加を抑え、触媒の交換時間間隔を延長する
ことができるものである。
This suppresses the increase in the pressure loss of the reaction gas due to the fragmentation caused by the destruction of the catalyst, and makes it possible to extend the time interval for replacing the catalyst.

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

図は本発明の一実施例を示したもので第1図は触媒反応
装置の一例である燃料電池装置のリフオーマの全体断面
図、第2図は第1図の■−■断面図、第3図は第1図の
要部拡大図、第4図は第3図のIV−IV断面図、第5
V!iは本発明の動作説明図である。 1・・・内筒、2・・・内筒、3・・・触媒、4・・・
ギャップ、5・・・触媒目皿、6・・・胴、7・・・バ
ーナ、8・・・断熱材、9・・・反応ガス、10・・・
改質ガス、12・・・第1の支持体、13・・・第2の
支持体。 第1因 竿5図 CB)         CC) (F))(E)
The drawings show one embodiment of the present invention. Fig. 1 is an overall sectional view of a re-former of a fuel cell device which is an example of a catalytic reaction device, Fig. 2 is a sectional view taken along the line ■-■ of Fig. 1, and Fig. 3 The figure is an enlarged view of the main part of Figure 1, Figure 4 is a sectional view taken along line IV-IV in Figure 3, and Figure 5 is an enlarged view of the main part of Figure 1.
V! i is an explanatory diagram of the operation of the present invention. 1... Inner cylinder, 2... Inner cylinder, 3... Catalyst, 4...
Gap, 5... Catalyst plate, 6... Body, 7... Burner, 8... Insulation material, 9... Reactant gas, 10...
Reformed gas, 12...first support, 13...second support. 1st factor diagram 5 CB) CC) (F)) (E)

Claims (1)

【特許請求の範囲】 1、内筒、該内筒と同心的に配置された外筒、前記内筒
の外周面と前記外筒の内周面とで形成される空間部に封
入された触媒、前記触媒を前記内・外筒の下端で保持す
る触媒保持手段を具え、被反応ガスを前記触媒を通過さ
せるように導入させ、前記触媒を通過させた反応ガスを
、前記内筒を介して外部へ導出するように構成した触媒
反応装置において、前記触媒保持手段を皿部と、該皿部
を前記外筒で保持する第1の支持手段と、前記内筒で保
持する第2の支持体とで構成し、前記第1の支持体を前
記外筒の内周面に、前記第2の支持体を前記内筒の外周
面に固着せしめ、前記皿部を前記第1、第2の支持体に
載置したことを特徴とする触媒反応装置。 2、前記内筒、前記外筒が断面円形状に形成されている
特許請求の範囲第1項記載の触媒反応装置。 3、前記外筒の一端は開口し、他端は閉塞し、前記内筒
の一端は、前記反応ガスを導出する手段に連結し、他端
を前記外筒の閉塞部近傍に開口して成る特許請求の範囲
第1項記載の触媒反応装置。 4、前記内・外筒とから成る反応部を複数本並設し、こ
れらをシェル内に収納してなる特許請求の範囲第3項記
載の触媒反応装置。
[Claims] 1. An inner cylinder, an outer cylinder arranged concentrically with the inner cylinder, and a catalyst sealed in a space formed by the outer peripheral surface of the inner cylinder and the inner peripheral surface of the outer cylinder. , comprising a catalyst holding means for holding the catalyst at the lower ends of the inner and outer cylinders, introducing the gas to be reacted so as to pass through the catalyst, and directing the reaction gas that has passed through the catalyst through the inner cylinder. In a catalytic reaction device configured to lead out to the outside, the catalyst holding means is a dish portion, a first support means that holds the dish portion with the outer cylinder, and a second support body that holds the catalyst holding means with the inner cylinder. The first support is fixed to the inner peripheral surface of the outer cylinder, the second support is fixed to the outer peripheral surface of the inner cylinder, and the dish part is fixed to the first and second supports. A catalytic reaction device characterized by being placed on the body. 2. The catalytic reaction device according to claim 1, wherein the inner cylinder and the outer cylinder are formed to have a circular cross section. 3. One end of the outer cylinder is open and the other end is closed, one end of the inner cylinder is connected to a means for introducing the reaction gas, and the other end is opened near the closed part of the outer cylinder. A catalytic reaction apparatus according to claim 1. 4. The catalytic reaction device according to claim 3, wherein a plurality of reaction sections each comprising the inner and outer cylinders are arranged in parallel and housed in a shell.
JP59234960A 1984-11-09 1984-11-09 Catalytic reaction apparatus Granted JPS61114730A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59234960A JPS61114730A (en) 1984-11-09 1984-11-09 Catalytic reaction apparatus

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59234960A JPS61114730A (en) 1984-11-09 1984-11-09 Catalytic reaction apparatus

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP3007556A Division JPH0685866B2 (en) 1991-01-25 1991-01-25 Catalytic reactor

Publications (2)

Publication Number Publication Date
JPS61114730A true JPS61114730A (en) 1986-06-02
JPH0365228B2 JPH0365228B2 (en) 1991-10-11

Family

ID=16978949

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59234960A Granted JPS61114730A (en) 1984-11-09 1984-11-09 Catalytic reaction apparatus

Country Status (1)

Country Link
JP (1) JPS61114730A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0450101A (en) * 1990-06-18 1992-02-19 Fuji Electric Co Ltd Fuel reformer
JP2005089209A (en) * 2003-09-12 2005-04-07 Nippon Oil Corp Reforming equipment, and fuel cell system
JP2006223971A (en) * 2005-02-16 2006-08-31 Tokyo Gas Co Ltd Annular reactor, its preparing method, and sealing method
JP2009084141A (en) * 2007-09-13 2009-04-23 Nippon Oil Corp Reforming apparatus
JP2009209006A (en) * 2008-03-05 2009-09-17 Aisin Seiki Co Ltd Gas treatment apparatus for fuel cell
JP2010235403A (en) * 2009-03-31 2010-10-21 Ebara Corp Reformer
JP2011213562A (en) * 2010-04-02 2011-10-27 Yasuo Ishikawa Hydrogen generation unit for generating hydrogen from water

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS503267A (en) * 1973-05-11 1975-01-14
JPS58137440U (en) * 1982-03-10 1983-09-16 バブコツク日立株式会社 Reformer for fuel cells

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS503267A (en) * 1973-05-11 1975-01-14
JPS58137440U (en) * 1982-03-10 1983-09-16 バブコツク日立株式会社 Reformer for fuel cells

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0450101A (en) * 1990-06-18 1992-02-19 Fuji Electric Co Ltd Fuel reformer
JP2005089209A (en) * 2003-09-12 2005-04-07 Nippon Oil Corp Reforming equipment, and fuel cell system
JP2006223971A (en) * 2005-02-16 2006-08-31 Tokyo Gas Co Ltd Annular reactor, its preparing method, and sealing method
JP2009084141A (en) * 2007-09-13 2009-04-23 Nippon Oil Corp Reforming apparatus
JP2009209006A (en) * 2008-03-05 2009-09-17 Aisin Seiki Co Ltd Gas treatment apparatus for fuel cell
JP2010235403A (en) * 2009-03-31 2010-10-21 Ebara Corp Reformer
JP4657351B2 (en) * 2009-03-31 2011-03-23 株式会社荏原製作所 Reformer
JP2011213562A (en) * 2010-04-02 2011-10-27 Yasuo Ishikawa Hydrogen generation unit for generating hydrogen from water

Also Published As

Publication number Publication date
JPH0365228B2 (en) 1991-10-11

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