JPH0620711A - Inside reform unit for indirectly inside-reforming fused carbonate type fuel cell - Google Patents
Inside reform unit for indirectly inside-reforming fused carbonate type fuel cellInfo
- Publication number
- JPH0620711A JPH0620711A JP4179831A JP17983192A JPH0620711A JP H0620711 A JPH0620711 A JP H0620711A JP 4179831 A JP4179831 A JP 4179831A JP 17983192 A JP17983192 A JP 17983192A JP H0620711 A JPH0620711 A JP H0620711A
- Authority
- JP
- Japan
- Prior art keywords
- reforming
- partition plate
- internal reforming
- fuel cell
- raw material
- 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
- 238000002407 reforming Methods 0.000 title claims abstract description 97
- 239000000446 fuel Substances 0.000 title claims abstract description 20
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 title claims abstract description 19
- 238000005192 partition Methods 0.000 claims abstract description 36
- 239000003054 catalyst Substances 0.000 claims abstract description 30
- 239000002994 raw material Substances 0.000 claims description 30
- 238000007789 sealing Methods 0.000 claims description 14
- 239000000463 material Substances 0.000 abstract 3
- 239000007789 gas Substances 0.000 description 69
- 238000000926 separation method Methods 0.000 description 6
- 239000003792 electrolyte Substances 0.000 description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
- 239000010935 stainless steel Substances 0.000 description 4
- 229910001220 stainless steel Inorganic materials 0.000 description 4
- 238000000034 method Methods 0.000 description 3
- 238000006057 reforming reaction Methods 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 239000000919 ceramic Substances 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 230000002093 peripheral effect Effects 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 238000010248 power generation Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229910000990 Ni alloy Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 229910010293 ceramic material Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005496 eutectics Effects 0.000 description 1
- 239000002737 fuel gas Substances 0.000 description 1
- YQNQTEBHHUSESQ-UHFFFAOYSA-N lithium aluminate Chemical compound [Li+].[O-][Al]=O YQNQTEBHHUSESQ-UHFFFAOYSA-N 0.000 description 1
- XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 description 1
- 229910052808 lithium carbonate Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910000480 nickel oxide Inorganic materials 0.000 description 1
- GNRSAWUEBMWBQH-UHFFFAOYSA-N oxonickel Chemical compound [Ni]=O GNRSAWUEBMWBQH-UHFFFAOYSA-N 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 230000036647 reaction Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
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
-
- 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
- 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
Description
【0001】[0001]
【産業上の利用分野】本発明は間接内部改質溶融炭酸塩
型燃料電池の内部改質ユニットに関し、特に内部改質ユ
ニットの原料ガス仕切板の構造の改良に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an internal reforming unit for an indirect internal reforming molten carbonate fuel cell, and more particularly to improving the structure of a raw material gas partition plate of the internal reforming unit.
【0002】[0002]
【従来の技術】溶融炭酸塩型燃料電池は作動温度が約6
50℃と高温であり、通常燃料として使用される天然ガ
ス(主成分:メタン)の改質温度である800℃に近い
ため、電池スタック内で燃料の改質を行う内部改質方式
が可能である。この内部改質方式は、燃料改質装置が不
要であるためコンパクト化が可能であると共に、電池反
応の際に生じる熱や水を、改質反応に必要な熱や水とし
て利用することができる等の優れた特長があるため外部
改質方式に比べて高い発電効率が期待できる。2. Description of the Related Art A molten carbonate fuel cell has an operating temperature of about 6
Since the temperature is as high as 50 ° C and is close to 800 ° C, which is the reforming temperature of natural gas (main component: methane) normally used as a fuel, an internal reforming method for reforming the fuel in the cell stack is possible. is there. This internal reforming system can be made compact because a fuel reforming device is unnecessary, and heat and water generated during the cell reaction can be used as heat and water necessary for the reforming reaction. Due to such excellent features, higher power generation efficiency can be expected compared to the external reforming method.
【0003】この内部改質方式は、改質触媒の配置方法
により直接内部改質方式と,間接内部改質方式とに分類
される。前者は、燃料極背面の燃料ガス通路に改質触媒
を設置した電池であり、水素が消費される場所に改質触
媒が設けられているため改質効率が高くより高い発電効
率が期待できるが、改質触媒が電解質中の溶融炭酸塩に
より汚染されやすく特性劣化が大きいという問題があ
る。一方、後者は、数セル(通常3〜6セル)毎に改質
触媒を充填した改質容器を設置した電池であり、改質容
器(即ち、改質触媒)と電解質(即ち、溶融炭酸塩)と
が隔離して配置されているため、前者のような溶融炭酸
塩による改質触媒の汚染の問題がなく長寿命が期待でき
るという特長がある。The internal reforming system is classified into a direct internal reforming system and an indirect internal reforming system depending on the method of arranging the reforming catalyst. The former is a cell in which a reforming catalyst is installed in the fuel gas passage on the back of the fuel electrode, and since the reforming catalyst is installed in a place where hydrogen is consumed, higher reforming efficiency and higher power generation efficiency can be expected. However, there is a problem that the reforming catalyst is easily contaminated by the molten carbonate in the electrolyte and the characteristics are largely deteriorated. On the other hand, the latter is a battery in which a reforming container filled with a reforming catalyst is installed in every few cells (usually 3 to 6 cells), and the reforming container (that is, the reforming catalyst) and the electrolyte (that is, molten carbonate). ) And are separated from each other, there is no problem of contamination of the reforming catalyst by the molten carbonate as in the former, and a long life can be expected.
【0004】ところで、従来の間接内部改質溶融炭酸塩
型燃料電池に用いられる内部改質ユニットは、図5及び
図6に示すように、原料ガスを改質ユニット内に導入す
る原料ガス導入管61と,改質ユニット内での改質反応
が均一になるように前記原料ガス導入管61から導入さ
れた原料ガスの流れを制御する原料ガス仕切板71と,
この原料ガス仕切板71の周囲に配される改質触媒部8
4(即ち、コルゲート板82とガス分離板83との積層
部)と、この改質触媒部84の周面を取り囲む額縁状の
枠体100とから成る内部改質ユニット本体と、この内
部改質ユニット本体の上下両面に取り付けられる密閉板
110a・110bとから構成されている。前記原料ガ
ス仕切板71は、前記枠体100と高さ寸法が同じにな
るように構成され、制御壁71の上下両面はそれぞれ上
下の密閉板110a・110bに溶接され、制御壁71
の一端は前記枠体100の内面に溶接されている。By the way, as shown in FIGS. 5 and 6, the internal reforming unit used in the conventional indirect internal reforming molten carbonate fuel cell has a raw material gas introduction pipe for introducing the raw material gas into the reforming unit. 61, and a raw material gas partition plate 71 for controlling the flow of the raw material gas introduced from the raw material gas introduction pipe 61 so that the reforming reaction in the reforming unit becomes uniform.
Reforming catalyst section 8 arranged around this source gas partition plate 71
4 (that is, a laminated portion of the corrugated plate 82 and the gas separation plate 83) and a frame-shaped frame body 100 that surrounds the peripheral surface of the reforming catalyst portion 84, and the internal reforming unit main body. It is composed of sealing plates 110a and 110b attached to both upper and lower surfaces of the unit body. The source gas partition plate 71 is configured to have the same height dimension as that of the frame body 100, and the upper and lower surfaces of the control wall 71 are welded to the upper and lower sealing plates 110a and 110b, respectively.
One end of is welded to the inner surface of the frame 100.
【0005】[0005]
【発明が解決しようとする課題】ところが、上記図5及
び図6に示した従来の内部改質ユニットは、内部改質ユ
ニット本体の上下両面を、上下の密閉板110a・11
0bを取り付けてスタックを構成する際に、以下のよう
な問題が生じる。即ち、前記枠体100と原料ガス仕切
板71との間に設けられる改質触媒部84の高さ寸法
が、前記枠体100,及び原料ガス仕切板71の高さ寸
法よりも低い場合には、上下の密閉板110a・110
bを取り付ける際に前記原料ガス仕切板71に締め付け
圧力が集中してかかることになる。したがって、内部改
質ユニットと各電極とが均一に接触せずに前記原料ガス
仕切板71,及び枠体100に相当する領域に集中して
電流が流れるので、安定した電池特性を得ることができ
ないという課題を有する。尚、前記改質触媒部84の高
さ寸法が、前記枠体100,及び原料ガス仕切板71の
高さ寸法よりも高い場合には、上下の密閉板110a・
110bを取り付けてスタックを構成する際に、弾力性
を有する前記改質触媒部84が前記枠体100,及び原
料ガス仕切板71の高さ寸法と略同じ高さになるまで収
縮する。したがって、締め付け圧力が略均等に分散する
ため、前記のような問題は生じない。However, in the conventional internal reforming unit shown in FIGS. 5 and 6, the upper and lower sealing plates 110a.
When attaching 0b to form a stack, the following problems occur. That is, when the height dimension of the reforming catalyst portion 84 provided between the frame body 100 and the source gas partition plate 71 is lower than the height dimension of the frame body 100 and the source gas partition plate 71. , Upper and lower sealing plates 110a, 110
When attaching b, the tightening pressure is concentrated on the source gas partition plate 71. Therefore, the internal reforming unit and each electrode do not come into uniform contact with each other, and the current flows concentratedly in the region corresponding to the source gas partition plate 71 and the frame body 100, so that stable battery characteristics cannot be obtained. Has the problem. When the height dimension of the reforming catalyst portion 84 is higher than the height dimension of the frame body 100 and the source gas partition plate 71, the upper and lower sealing plates 110a.
When 110b is attached to form a stack, the elastic reforming catalyst portion 84 contracts until the height is substantially the same as the height of the frame 100 and the source gas partition plate 71. Therefore, the tightening pressure is substantially evenly distributed, and the above-mentioned problem does not occur.
【0006】本発明は上記課題に鑑み、締め付け圧力を
略均等に分散させて、電極との均一な接触を得ることが
できる間接内部改質溶融炭酸塩型燃料電池の内部改質ユ
ニットを提供することを目的とする。In view of the above-mentioned problems, the present invention provides an internal reforming unit of an indirect internal reforming molten carbonate fuel cell, which can disperse tightening pressure substantially evenly and obtain uniform contact with an electrode. The purpose is to
【0007】[0007]
【課題を解決するための手段】本発明は上記課題を解決
するため、枠体内に改質触媒が充填され、この枠体内の
中央部に原料ガスの流れ方向を制御する原料ガス仕切板
を設けた内部改質ユニット本体と、この内部改質ユニッ
ト本体に取り付けられる上下の密閉板とを有する間接内
部改質溶融炭酸塩型燃料電池の内部改質ユニットにおい
て、上記原料ガス仕切板は、上下方向に弾性変形可能な
弾性部材で構成されていることを特徴とする。In order to solve the above-mentioned problems, the present invention is provided with a reforming catalyst in a frame body, and a raw material gas partition plate for controlling the flow direction of the raw material gas is provided in the central portion of the frame body. In the internal reforming unit of the indirect internal reforming molten carbonate fuel cell having the internal reforming unit main body and the upper and lower sealing plates attached to the internal reforming unit main body, the source gas partition plate is arranged in the vertical direction. It is characterized in that it is composed of an elastic member that is elastically deformable.
【0008】[0008]
【作用】上記構成によれば、原料ガス仕切板が弾性部材
で構成されているので、改質触媒部(即ち、コルゲート
板と分離板との積層部)の高さ寸法が前記原料ガス仕切
板の高さ寸法よりも低い場合でも、改質触媒部(即ち、
コルゲート板と分離板との積層部)と同じ高さ寸法にな
るように弾性変形する。したがって、上下の密閉板を取
り付けてスタックを構成する場合に、締め付け圧力が従
来のように、原料ガス仕切板に集中することがなく略均
等に分散することになる。その結果、内部改質ユニット
が各電極と略均一に接触することになるので、長期にわ
たって安定した電池特性を得ることができる。According to the above structure, since the raw material gas partition plate is made of the elastic member, the height dimension of the reforming catalyst portion (that is, the laminated portion of the corrugated plate and the separation plate) is the raw material gas partition plate. The height of the reforming catalyst section (ie,
It is elastically deformed so that it has the same height as the laminated portion of the corrugated plate and the separation plate. Therefore, when the upper and lower sealing plates are attached to form a stack, the tightening pressure is not concentrated on the source gas partition plate as in the conventional case, but is substantially evenly distributed. As a result, the internal reforming unit comes into contact with each electrode substantially uniformly, so that stable battery characteristics can be obtained for a long period of time.
【0009】[0009]
(第一実施例)図1は本発明の第一実施例に係る内部改
質ユニットを用いた間接内部改質溶融炭酸塩型燃料電池
の概略図、図2は内部改質ユニットの分解斜視図、図3
は図2の内部改質ユニットのA−A線断面図である。こ
の間接内部改質溶融炭酸塩型燃料電池は、図1に示すよ
うに、電解質を挟んでアノードとカソードとを配置した
単セル(いずれも図示せず)を、セパレータ(図示せ
ず)を介して複数積層させ、且つ、改質触媒を充填した
内部改質ユニット1を数セル(例えば、5セル)毎に介
挿させて成るスタック2を、上下の締付板3a・3bを
介してスプリング4a・4b,及びナット5a・5bで
締め付けた構造である。尚、前記スタック2の各側面に
は、セラミックス製の絶縁フレーム(図示せず)を介し
てステンレス製のマニホールド(図示せず)がそれぞれ
取り付けられている。(First Embodiment) FIG. 1 is a schematic view of an indirect internal reforming molten carbonate fuel cell using an internal reforming unit according to the first embodiment of the present invention, and FIG. 2 is an exploded perspective view of the internal reforming unit. , Fig. 3
FIG. 3 is a sectional view of the internal reforming unit of FIG. 2 taken along the line AA. In this indirect internal reforming molten carbonate fuel cell, as shown in FIG. 1, a single cell (neither is shown) in which an anode and a cathode are arranged with an electrolyte sandwiched is provided via a separator (not shown). A stack 2 formed by stacking a plurality of internal reforming units 1 filled with a reforming catalyst every several cells (for example, 5 cells), and springs through upper and lower tightening plates 3a and 3b. 4a and 4b and nuts 5a and 5b. A stainless steel manifold (not shown) is attached to each side surface of the stack 2 via a ceramic insulating frame (not shown).
【0010】上記単セルは、炭酸リチウムと炭酸カリウ
ムとの共晶塩をリチウムアルミネートを主成分とした多
孔質セラミックス材中に保持した電解質板を挟んで、ニ
ッケルとアルミニウムとの合金から成るアノードと,酸
化ニッケル焼結体を主体とするカソードとを配置した構
造である。各単セルのアノードは、前記セパレータによ
って、隣接する単セルのカソードと電気的に接続してい
て、これによって積層した全ての単セルが電気的に直列
に接続することになる。The above-mentioned single cell is an anode made of an alloy of nickel and aluminum with an electrolyte plate in which a eutectic salt of lithium carbonate and potassium carbonate is held in a porous ceramic material containing lithium aluminate as a main component. And a cathode mainly composed of a nickel oxide sintered body. The anode of each unit cell is electrically connected to the cathode of the adjacent unit cell by the separator, and thereby all the unit cells stacked are electrically connected in series.
【0011】上記内部改質ユニット1は、図2に示すよ
うに、原料ガスを改質ユニット内に導入する原料ガス導
入管6と,改質ユニット内での改質反応が均一になるよ
うに前記原料ガス導入管6から導入された原料ガスの流
れを制御するステンレス製の原料ガス仕切板7と,この
原料ガス仕切板7の周囲に配される改質触媒部8と、こ
の改質触媒部8の周面を取り囲む額縁状の枠体10とか
ら成る内部改質ユニット本体と、この内部改質ユニット
本体の上下両面に締め付けられる密閉板11a・11b
とから構成されている。尚、前記枠体10の側面には、
改質後の水素を主成分とするガスをアノードガスリター
ンマニホールド(図示せず)に排出する複数(図示例で
は4個)の改質ガス排出口10aが設けられている。As shown in FIG. 2, the internal reforming unit 1 and the raw material gas introducing pipe 6 for introducing the raw material gas into the reforming unit and the reforming reaction in the reforming unit are made uniform. A raw material gas partition plate 7 made of stainless steel for controlling the flow of the raw material gas introduced from the raw material gas introduction pipe 6, a reforming catalyst section 8 arranged around the raw material gas partition plate 7, and this reforming catalyst. An internal reforming unit main body including a frame-shaped frame body 10 surrounding the peripheral surface of the portion 8, and sealing plates 11a and 11b that are fastened to both upper and lower surfaces of the internal reforming unit main body.
It consists of and. In addition, on the side surface of the frame body 10,
A plurality of (four in the illustrated example) reformed gas discharge ports 10a for discharging the reformed gas containing hydrogen as a main component to an anode gas return manifold (not shown) are provided.
【0012】上記原料ガス仕切板7は、図3に示すよう
に、制御壁7の上下両面は上下の密閉板11a・11b
とそれぞれ溶接され、一端は前記枠体10の内面と溶接
されている。また、この原料ガス仕切板7は、ステンレ
スを側面視Σ状に折り曲げられて構成されているので、
上下の密閉板11a・11bで締め付けてスタックを構
成する場合には、前記改質触媒部8と同じ高さ寸法にな
るように変形する。したがって、改質触媒部の高さ寸法
が、前記枠体10,及び原料ガス仕切板7の高さ寸法よ
りも低い場合でも、従来のように締め付け圧力が原料ガ
ス仕切板7に集中することがなく略均等に分散すること
になる。その結果、内部改質ユニットが各電極と略均一
に接触することになるので、長期にわたって安定した電
池特性を得ることができる。As shown in FIG. 3, the source gas partition plate 7 has upper and lower sealing plates 11a and 11b on both upper and lower sides of the control wall 7.
Are welded together, and one end is welded to the inner surface of the frame 10. Further, since the source gas partition plate 7 is formed by bending stainless steel into a Σ shape in a side view,
When the upper and lower sealing plates 11a and 11b are tightened to form a stack, the stack is deformed to have the same height as the reforming catalyst section 8. Therefore, even when the height dimension of the reforming catalyst portion is lower than the height dimension of the frame body 10 and the raw material gas partition plate 7, the tightening pressure can be concentrated on the raw material gas partition plate 7 as in the conventional case. Instead, it will be distributed almost evenly. As a result, the internal reforming unit comes into contact with each electrode substantially uniformly, so that stable battery characteristics can be obtained for a long period of time.
【0013】上記改質触媒部8は、図3に示すように、
改質触媒(例えば、ニッケル系触媒)を保持したコルゲ
ート板80と,ガス分離板81とが積層された構造であ
り、前記改質触媒部8の高さ寸法が、前記枠体10,及
び原料ガス仕切板7の高さ寸法よりも高い場合でも、上
下の密閉板11a・11bを取り付ける際に、弾力性を
有する前記改質触媒部8が前記枠体10,及び原料ガス
仕切板7の高さ寸法と略同じ高さになるまで収縮する。
したがって、締め付け圧力が略均等に分散するため、前
記のような問題は生じない。 〔その他の事項〕上記実施例においては、原料ガス仕切
板7は、Σ状に折り曲げて構成したが、本発明は何らこ
れに限定されるものではなく、例えば、Z状や階段状等
の形状にすることも勿論可能である。The reforming catalyst section 8 is, as shown in FIG.
It has a structure in which a corrugated plate 80 holding a reforming catalyst (for example, a nickel-based catalyst) and a gas separation plate 81 are laminated, and the height dimension of the reforming catalyst portion 8 is the frame body 10 and the raw material. Even when the height of the gas partition plate 7 is higher than the height of the gas partition plate 7, when the upper and lower sealing plates 11a and 11b are attached, the reforming catalyst portion 8 having elasticity has the height of the frame body 10 and the raw material gas partition plate 7. It contracts until the height is almost the same as the height.
Therefore, the tightening pressure is substantially evenly distributed, and the above-mentioned problem does not occur. [Other Matters] In the above embodiment, the source gas partition plate 7 was formed by bending in a Σ shape, but the present invention is not limited to this, and for example, a Z shape, a step shape, or the like. Of course, it is also possible.
【0014】(第二実施例)図4は本発明の第二実施例
に係る内部改質ユニットを用いた間接内部改質溶融炭酸
塩型燃料電池の概略平面図である。尚、上記第一実施例
と同様の機能を有する構成部分については同一番号を付
して説明を省略する。この間接内部改質溶融炭酸塩型燃
料電池の各側面には、セラミックス製の絶縁フレーム
(図示せず)を介してステンレス製のアノードガスリタ
ーンマニホールド14,アノードガス排出マニホールド
15,カソードガス供給マニホールド16,カソードガ
ス排出マニホールド17がそれぞれ取り付けられてい
る。また、前記アノードガス排出マニホールド15には
アノードガス排出管18が、カソードガス供給マニホー
ルド16にはカソードガス供給管19が、カソードガス
排出マニホールド17にはカソードガス排出管20がそ
れぞれ接続されている。(Second Embodiment) FIG. 4 is a schematic plan view of an indirect internal reforming molten carbonate fuel cell using an internal reforming unit according to a second embodiment of the present invention. The constituent parts having the same functions as those of the first embodiment are designated by the same reference numerals and the description thereof will be omitted. On each side surface of this indirect internal reforming molten carbonate fuel cell, an anode gas return manifold 14, an anode gas discharge manifold 15, and a cathode gas supply manifold 16 made of stainless steel are provided via an insulating frame (not shown) made of ceramics. , And a cathode gas exhaust manifold 17 is attached. An anode gas exhaust pipe 18 is connected to the anode gas exhaust manifold 15, a cathode gas supply pipe 19 is connected to the cathode gas supply manifold 16, and a cathode gas exhaust pipe 20 is connected to the cathode gas exhaust manifold 17.
【0015】上記内部改質ユニット1は、原料ガス仕切
板7が、L型の原料ガス仕切板7aと,直線状の原料ガ
ス仕切板7bとに分割され、且つ、改質ガス排出口12
が枠体10に1個のみ設けられ、上記第一実施例の改質
ガス排出口10aよりも十分小さくなっており、前記改
質ガス排出口12近傍のアノードガスリターンマニホー
ルド14内には、バッフル板13が取り付けられている
他は、上記第一実施例の内部改質ユニット1と略同様の
構成である。In the internal reforming unit 1, the raw material gas partition plate 7 is divided into an L-shaped raw material gas partition plate 7a and a linear raw material gas partition plate 7b, and the reformed gas discharge port 12 is provided.
Is provided in the frame body 10 and is sufficiently smaller than the reformed gas discharge port 10a of the first embodiment, and the baffle is provided in the anode gas return manifold 14 near the reformed gas discharge port 12. Except that the plate 13 is attached, it has substantially the same configuration as the internal reforming unit 1 of the first embodiment.
【0016】上記第二実施例によれば、改質ガス排出口
12が十分小さく構成されているので、改質ユニット1
内の圧力損失が十分大きくなる。したがって、改質ユニ
ット1の製造精度による圧力損失を十分無視することが
可能になり、スタック2内に設置された各改質ユニット
1へ原料ガスを略均一に分配することができる。また、
カソードガス排出側近傍の高温部を原料ガスが流れるた
め、原料ガス改質率を向上させることができる。According to the second embodiment described above, since the reformed gas discharge port 12 is configured to be sufficiently small, the reforming unit 1
The pressure loss inside is sufficiently large. Therefore, the pressure loss due to the manufacturing accuracy of the reforming unit 1 can be sufficiently ignored, and the raw material gas can be distributed substantially uniformly to each reforming unit 1 installed in the stack 2. Also,
Since the raw material gas flows through the high temperature portion near the cathode gas discharge side, the raw material gas reforming rate can be improved.
【0017】更に、改質ガス排出口12の近傍にはバッ
フル板13が設けられているので、改質ガスをアノード
ガスリターンマニホールド14で均等に分散させ、スタ
ック2内の各セルへの改質ガスを略均等に分配すること
ができる。Further, since the baffle plate 13 is provided in the vicinity of the reformed gas discharge port 12, the reformed gas is evenly dispersed in the anode gas return manifold 14 to reform the cells in the stack 2. The gas can be distributed substantially evenly.
【0018】[0018]
【発明の効果】以上の本発明によれば、原料ガス仕切板
が弾性部材で構成されているので、改質触媒部(即ち、
コルゲート板と分離板との積層部)の高さ寸法が前記原
料ガス仕切板の高さ寸法よりも低い場合でも、改質触媒
部(即ち、コルゲート板と分離板との積層部)と同じ高
さ寸法になるように弾性変形する。したがって、上下の
密閉板で締め付けてスタックを構成する場合に、締め付
け圧力が従来のように、原料ガス仕切板に集中すること
がなく略均等に分散することになる。その結果、内部改
質ユニットが各電極と略均一に接触することになるの
で、長期にわたって安定した電池特性を得ることができ
るといった優れた効果を奏する。As described above, according to the present invention, since the source gas partition plate is composed of the elastic member, the reforming catalyst portion (that is,
Even if the height dimension of the laminated portion of the corrugated plate and the separation plate is lower than the height dimension of the raw material gas partition plate, the same height as the reforming catalyst portion (that is, the laminated portion of the corrugated plate and the separation plate). Elastically deforms to the desired size. Therefore, when the stack is constructed by tightening the upper and lower sealing plates, the tightening pressure is not concentrated on the source gas partition plate as in the conventional case, but is distributed substantially evenly. As a result, the internal reforming unit comes into contact with each electrode substantially uniformly, which brings about an excellent effect that stable battery characteristics can be obtained for a long period of time.
【図面の簡単な説明】[Brief description of drawings]
【図1】本発明の第一実施例に係る内部改質ユニットを
用いた間接内部改質溶融炭酸塩型燃料電池の概略図であ
る。FIG. 1 is a schematic view of an indirect internal reforming molten carbonate fuel cell using an internal reforming unit according to a first embodiment of the present invention.
【図2】本発明の第一実施例に係る内部改質ユニットの
分解斜視図である。FIG. 2 is an exploded perspective view of an internal reforming unit according to the first embodiment of the present invention.
【図3】図2の内部改質ユニットのA−A線断面図であ
る。3 is a cross-sectional view of the internal reforming unit of FIG. 2 taken along the line AA.
【図4】本発明の第二実施例に係る内部改質ユニットを
用いた間接内部改質溶融炭酸塩型燃料電池の概略平面図
である。FIG. 4 is a schematic plan view of an indirect internal reforming molten carbonate fuel cell using an internal reforming unit according to a second embodiment of the present invention.
【図5】従来の内部改質ユニットの分解斜視図である。FIG. 5 is an exploded perspective view of a conventional internal reforming unit.
【図6】図5の内部改質ユニットのX−X線断面図であ
る。6 is a cross-sectional view taken along line XX of the internal reforming unit of FIG.
1 内部改質ユニット 7 原料ガス仕切板 8 改質触媒部 10 枠体 11a・11b 密閉板 1 Internal Reforming Unit 7 Raw Material Gas Partition Plate 8 Reforming Catalyst Section 10 Frame 11a / 11b Sealing Plate
───────────────────────────────────────────────────── フロントページの続き (72)発明者 斎藤 俊彦 守口市京阪本通2丁目18番地 三洋電機株 式会社内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Toshihiko Saito 2-18 Keihan Hondori, Moriguchi-shi Sanyo Electric Co., Ltd.
Claims (1)
体内の中央部に原料ガスの流れ方向を制御する原料ガス
仕切板を設けた内部改質ユニット本体と、この内部改質
ユニット本体に取り付けられる上下の密閉板とを有する
間接内部改質溶融炭酸塩型燃料電池の内部改質ユニット
において、 上記原料ガス仕切板は、上下方向に弾性変形可能な弾性
部材で構成されていることを特徴とする間接内部改質溶
融炭酸塩型燃料電池の内部改質ユニット。1. An internal reforming unit main body in which a reforming catalyst is filled in a frame body, and a raw material gas partition plate for controlling a flow direction of the raw material gas is provided in a central portion of the frame body, and the internal reforming unit main body. In an internal reforming unit of an indirect internal reforming molten carbonate fuel cell having upper and lower sealing plates attached to, the source gas partition plate is composed of an elastic member that is elastically deformable in the vertical direction. Indirect internal reforming Characteristic Internal reforming unit of molten carbonate fuel cell.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4179831A JPH0620711A (en) | 1992-07-07 | 1992-07-07 | Inside reform unit for indirectly inside-reforming fused carbonate type fuel cell |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4179831A JPH0620711A (en) | 1992-07-07 | 1992-07-07 | Inside reform unit for indirectly inside-reforming fused carbonate type fuel cell |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0620711A true JPH0620711A (en) | 1994-01-28 |
Family
ID=16072662
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4179831A Pending JPH0620711A (en) | 1992-07-07 | 1992-07-07 | Inside reform unit for indirectly inside-reforming fused carbonate type fuel cell |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0620711A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH10275626A (en) * | 1997-03-31 | 1998-10-13 | Mitsubishi Electric Corp | Stacked fuel cell |
| WO2010104845A2 (en) | 2009-03-09 | 2010-09-16 | Fuelcell Energy, Inc. | Internally reforming fuel cell assembly with staged fuel flow and selective catalyst loading for improved temperature uniformity and efficiency |
-
1992
- 1992-07-07 JP JP4179831A patent/JPH0620711A/en active Pending
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH10275626A (en) * | 1997-03-31 | 1998-10-13 | Mitsubishi Electric Corp | Stacked fuel cell |
| WO2010104845A2 (en) | 2009-03-09 | 2010-09-16 | Fuelcell Energy, Inc. | Internally reforming fuel cell assembly with staged fuel flow and selective catalyst loading for improved temperature uniformity and efficiency |
| EP2406846A4 (en) * | 2009-03-09 | 2014-07-30 | Fuelcell Energy Inc | INTERNAL REFORMING FUEL CELL ASSEMBLY WITH STREAMED FUEL FLOW AND SELECTIVE CATALYST LOADING TO IMPROVE TEMPERATURE UNIFORMITY AND PERFORMANCE |
| KR20180087464A (en) * | 2009-03-09 | 2018-08-01 | 퓨얼 셀 에너지, 인크 | Internally reforming fuel cell assembly with staged fuel flow and selective catalyst loading for improved temperature uniformity and efficiency |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US7799480B2 (en) | Fuel cell stack with dummy cell | |
| EP0408104B1 (en) | Separator plate for use in a gas fuel cell which comprises a set of electrodes, and also a stack of fuel cells | |
| EP2732499B1 (en) | Sofc stack with temperature adapted compression force means | |
| JP2023538597A (en) | electrochemical cell stack | |
| US9054350B2 (en) | Fuel cell stack | |
| US7163759B2 (en) | Solid oxide fuel cell stack assembly having tapered diffusion layers | |
| JPH0831322B2 (en) | Internal reforming fuel cell and power plant using the same | |
| US5811202A (en) | Hybrid molten carbonate fuel cell with unique sealing | |
| JPH10228918A (en) | End cell structure of fuel cell | |
| JP3546495B2 (en) | Cylindrical fuel cell | |
| JPH0620711A (en) | Inside reform unit for indirectly inside-reforming fused carbonate type fuel cell | |
| JP2022125885A (en) | Fuel battery cell and fuel battery stack | |
| JP3291719B2 (en) | Fuel cell separator | |
| US3615852A (en) | Fuel cell | |
| AU2005320011B8 (en) | Fuel cell system | |
| US8192894B2 (en) | Plate-laminating type fuel cell | |
| JP2024129527A (en) | Electrochemical reaction cell stack | |
| JPH06275305A (en) | Fuel cell | |
| US20060292432A1 (en) | Fuel cell and fuel cell stack | |
| RU2846382C1 (en) | Assembly unit of solid oxide fuel cell on perforated metal base of planar type and interconnector | |
| JPH05174858A (en) | Manifold fastening structure for fusion carbonate type fuel cell | |
| JPH02160372A (en) | Separator of fuel battery | |
| JPH0850911A (en) | Flat solid electrolyte fuel cell | |
| JPH0355763A (en) | Gas fuel battery and electrode for use in the same | |
| JP2002280052A (en) | Structure that applies load equally to each power generation cell of the fuel cell |