JPH04338101A - Method for starting fuel cell system - Google Patents

Method for starting fuel cell system

Info

Publication number
JPH04338101A
JPH04338101A JP3109068A JP10906891A JPH04338101A JP H04338101 A JPH04338101 A JP H04338101A JP 3109068 A JP3109068 A JP 3109068A JP 10906891 A JP10906891 A JP 10906891A JP H04338101 A JPH04338101 A JP H04338101A
Authority
JP
Japan
Prior art keywords
fuel cell
hydrogen
cell system
steam reforming
starting
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.)
Withdrawn
Application number
JP3109068A
Other languages
Japanese (ja)
Inventor
Yoshimasa Fujimoto
芳正 藤本
Kazuto Kobayashi
一登 小林
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mitsubishi Heavy Industries Ltd
Original Assignee
Mitsubishi Heavy Industries Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Mitsubishi Heavy Industries Ltd filed Critical Mitsubishi Heavy Industries Ltd
Priority to JP3109068A priority Critical patent/JPH04338101A/en
Publication of JPH04338101A publication Critical patent/JPH04338101A/en
Withdrawn legal-status Critical Current

Links

Classifications

    • 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
    • Y02E60/32Hydrogen storage
    • 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

  • Hydrogen, Water And Hydrids (AREA)
  • Fuel Cell (AREA)

Abstract

PURPOSE:To exclude use of a heating means such as a burner in starting the steam reformer for a fuel cell system. CONSTITUTION:A gas of high hydrogen content is produced by the reforming reaction in a steam reformer 1 heated by a catalyzed combustion chamber 3, and the product gas is supplied to the hydrogen electrode 7 of a solid high molecular electrolyte-type fuel cell 6 to generate power by this fuel cell system. When the system is started, the hydrogen generated from a hydrogen storage 11 contg. a hydrogen storage alloy is supplied to the catalyzed combustion chamber 3 of the reformer 1.

Description

【発明の詳細な説明】[Detailed description of the invention]

【0001】0001

【産業上の利用分野】本発明は触媒燃料方式の水蒸気改
質反応器を使用した燃料電池システムの起動方法に関す
る。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for starting a fuel cell system using a catalytic fuel type steam reforming reactor.

【0002】0002

【従来の技術】従来より、水蒸気改質反応器と固体高分
子電解質型燃料電池とを使用する燃料電池システムの実
用化が検討されている。ここで、水蒸気改質反応器は、
メタンやメタノール等の炭化水素や含酸素炭化水素から
なる原料ガスを、水蒸気改質反応とCOシフト反応とに
よって主に水素と二酸化炭素とに分解するものである。 また、固体高分子電解質型燃料電池は、水蒸気改質反応
器で生成した水素ガスを水素極へ供給すると共に空気又
は酸素を空気極へ供給することにより発電するものであ
る。
BACKGROUND OF THE INVENTION The practical application of a fuel cell system using a steam reforming reactor and a solid polymer electrolyte fuel cell has heretofore been studied. Here, the steam reforming reactor is
A raw material gas consisting of hydrocarbons and oxygen-containing hydrocarbons such as methane and methanol is decomposed into mainly hydrogen and carbon dioxide through a steam reforming reaction and a CO shift reaction. Furthermore, a solid polymer electrolyte fuel cell generates electricity by supplying hydrogen gas produced in a steam reforming reactor to a hydrogen electrode and also supplying air or oxygen to an air electrode.

【0003】このような燃料電池システムで発電するに
は、まず、水蒸気改質器を起動しなければならない。そ
して、水蒸気改質器の起動方法としては、バーナーによ
る直接加熱又は炭化水素を原料とする触媒燃料方法が知
られている。
[0003] In order to generate electricity with such a fuel cell system, the steam reformer must first be started. Known methods for starting a steam reformer include direct heating with a burner or a catalytic fuel method using hydrocarbons as a raw material.

【0004】0004

【発明が解決しようとする課題】しかしながら、バーナ
ーのよる直接加熱方式では、以下の欠点がある。■  
輻射熱により反応管壁の温度は局部的に800℃以上に
なるため、使用する材質が高価なものとなる。■  安
定な燃焼状態を得るためパイロットバーナー等失火対策
が必要となり、燃焼器の構造の複雑化,制御系の複雑化
が避けられない。
However, the direct heating method using a burner has the following drawbacks. ■
Because the temperature of the reaction tube wall locally increases to 800° C. or higher due to radiant heat, the material used becomes expensive. ■ In order to obtain a stable combustion state, measures against misfire such as a pilot burner are required, which inevitably complicates the structure of the combustor and the control system.

【0005】また、炭化水素を原料とする触媒燃焼方式
では、低温(約400℃以下)での触媒活性が著しく小
さいため、燃焼触媒部をバーナー加熱もしくはヒーター
加熱により400℃以上に昇温する必要がある。このた
め、バーナー加熱では前述の欠点があり、ヒーター加熱
では、改質反応温度(約500℃以下)が高温であるた
め、通常のシースヒーター等では著しく寿命が短く停止
毎に交換する必要があるという問題がある。
[0005] Furthermore, in the catalytic combustion method that uses hydrocarbons as raw materials, the catalytic activity at low temperatures (approximately 400°C or less) is extremely low, so it is necessary to raise the temperature of the combustion catalyst to 400°C or higher by heating with a burner or heater. There is. For this reason, burner heating has the disadvantages mentioned above, and heater heating has a high reforming reaction temperature (approximately 500°C or less), so ordinary sheath heaters have a significantly short lifespan and must be replaced every time the heater is stopped. There is a problem.

【0006】本発明はこのような事情に鑑み、上述した
ような欠点のない燃料電池システムの起動方法を提供す
ることを目的とする。
[0006] In view of these circumstances, it is an object of the present invention to provide a method for starting a fuel cell system that does not have the above-mentioned drawbacks.

【0007】[0007]

【課題を解決するための手段】前記目的を達成する本発
明に係る燃料電池システムの起動方法は、触媒燃焼方式
の水蒸気改質反応器にメタンやメタノール等の炭化水素
や含酸素炭化水素からなる原料を供給して水蒸気改質反
応により水素濃度が高いガスを製造し、該製造ガスを固
体高分子電解質型燃料電池に供給して発電する燃料電池
システムの起動に際し、水素吸蔵合金を内蔵する水素貯
蔵器から発生させた水素を上記水蒸気改質反応器に供給
して触媒燃料に使用することを特徴とする。
[Means for Solving the Problems] A method for starting a fuel cell system according to the present invention that achieves the above-mentioned object is a method for starting a fuel cell system according to the present invention, in which a catalytic combustion type steam reforming reactor is charged with hydrocarbons such as methane and methanol, or oxygen-containing hydrocarbons. When starting up a fuel cell system that supplies raw materials and produces gas with a high hydrogen concentration through a steam reforming reaction, and supplies the produced gas to a solid polymer electrolyte fuel cell to generate electricity, hydrogen containing a hydrogen storage alloy is used. The present invention is characterized in that hydrogen generated from the storage device is supplied to the steam reforming reactor and used as catalytic fuel.

【0008】[0008]

【作用】前記構成では起動時に水蒸気改質反応器の燃焼
触媒に水素貯蔵器からの水素を供給できるため、常温で
の触媒燃焼が可能である。したがって、炭化水素を原料
とするバーナー又はヒーターが不良となり、水蒸気改質
反応器の構造が簡単となる。また、触媒燃焼であること
により通常の燃焼範囲外での燃焼が可能なため温度制御
が簡単であり、局部的な加熱が防止できる。さらに、触
媒表面での燃焼反応であるため、外部からのバーナーお
よびヒーター加熱に比べ温度上昇が速い。
[Operation] With the above structure, hydrogen can be supplied from the hydrogen storage device to the combustion catalyst of the steam reforming reactor at startup, so that catalytic combustion can be performed at room temperature. Therefore, the burner or heater using hydrocarbon as a raw material becomes defective, and the structure of the steam reforming reactor becomes simple. In addition, catalytic combustion allows combustion outside the normal combustion range, making temperature control easy and preventing localized heating. Furthermore, since the combustion reaction occurs on the surface of the catalyst, the temperature rises faster than when heated by an external burner or heater.

【0009】[0009]

【実施例】以下、本発明を実施例に基づいて説明する。EXAMPLES The present invention will be explained below based on examples.

【0010】図1には本発明方法による燃料電池システ
ムの一例を示す。図1中、1は水蒸気改質反応器であり
、原料となるメタンガスと水蒸気とを混合して導入する
ための原料供給管2が連結されている。また、水蒸気改
質反応器1は改質反応に必要な熱源となる燃焼触媒室3
を具えている。そして、燃料触媒室3には定常運転時の
触媒反応の原料となるメタンを供給するための配管4が
連結されている。
FIG. 1 shows an example of a fuel cell system according to the method of the present invention. In FIG. 1, 1 is a steam reforming reactor, to which is connected a raw material supply pipe 2 for introducing a mixture of methane gas and steam as raw materials. In addition, the steam reforming reactor 1 has a combustion catalyst chamber 3 which is a heat source necessary for the reforming reaction.
It is equipped with A pipe 4 is connected to the fuel catalyst chamber 3 for supplying methane, which is a raw material for the catalytic reaction during steady operation.

【0011】水蒸気改質反応器1へ供給されたメタン及
び水蒸気は水蒸気改質反応により主に水素及び二酸化炭
素に分解され、一酸化炭素を二酸化炭素へ転化するCO
変成器5へ送られる。
Methane and steam supplied to the steam reforming reactor 1 are mainly decomposed into hydrogen and carbon dioxide by a steam reforming reaction, and CO converts carbon monoxide into carbon dioxide.
It is sent to transformer 5.

【0012】図中6は固体高分子電解質型燃料電池(以
下、燃料電池という)であり、水素極7及び空気極8を
有している。ここで、水素極7へは上記CO変成器5で
二酸化炭素及び水素に転化された水素ガスが導入され、
また、空気極8へはブロワ9を介して空気が導入されて
おり、水素極7へ導入された水素ガス及び空気極8へ導
入された空気が反応するとにより空気が発生する。
In the figure, reference numeral 6 denotes a solid polymer electrolyte fuel cell (hereinafter referred to as a fuel cell), which has a hydrogen electrode 7 and an air electrode 8. Here, hydrogen gas converted into carbon dioxide and hydrogen in the CO shift converter 5 is introduced into the hydrogen electrode 7,
Furthermore, air is introduced into the air electrode 8 via a blower 9, and air is generated when the hydrogen gas introduced into the hydrogen electrode 7 and the air introduced into the air electrode 8 react.

【0013】燃料電池6の水素極7からの排ガスは配管
10により燃焼触媒室3に導入されるようになっている
が、この配管10の途中には水素貯蔵器11が介装され
ている。水素貯蔵器11は水素吸蔵合金を具えて水素を
一時貯蔵できるものであり、定常運時(低負荷時)又は
停止時に一定量の水素を蓄えるようになっている。そし
て、水素の貯蔵を行う時以外には、水素極7からの排ガ
スはバイパス配管12を介して燃焼触媒室3へ送られる
ようになっている。なお、燃焼触媒室3へはブロワ9か
らの空気が空気供給管13を介して供給されており、ま
た、燃焼触媒室3からの燃焼排ガスは、燃焼排ガス排管
14から排出される。
Exhaust gas from the hydrogen electrode 7 of the fuel cell 6 is introduced into the combustion catalyst chamber 3 through a pipe 10, and a hydrogen storage device 11 is interposed in the middle of the pipe 10. The hydrogen storage device 11 is equipped with a hydrogen storage alloy and can temporarily store hydrogen, and is designed to store a certain amount of hydrogen during steady operation (during low load) or when stopped. When hydrogen is not being stored, the exhaust gas from the hydrogen electrode 7 is sent to the combustion catalyst chamber 3 via the bypass pipe 12. Note that air from the blower 9 is supplied to the combustion catalyst chamber 3 via an air supply pipe 13, and combustion exhaust gas from the combustion catalyst chamber 3 is discharged from a combustion exhaust gas exhaust pipe 14.

【0014】次に、上述した燃料電池システムの起動方
法を説明する。まず、建設時の起動は、予め水素を蓄え
た水素貯蔵器11若しくは外部からの水素を配管10を
介して燃焼触媒室3へ供給することにより燃焼触媒を加
熱する。そして、燃焼触媒の温度が500℃以上となっ
たところで徐々にメタンを配管4を介して供給し、水素
からメタンの切り換えを行う。水蒸気改質反応器1が所
定温度になった後、該水蒸気改質反応器1内に原料メタ
ンガスと原料水蒸気とを原料供給管2から供給し、シス
テムを安定させる。そして、低負荷時又はシステム停止
時に水素貯蔵器11に水素を蓄えて次回の起動用とし、
他の運転時には水素極7からの排ガスはバイパス配管1
2を介して燃焼触媒室3へ供給される。
Next, a method of starting up the above-mentioned fuel cell system will be explained. First, during construction, the combustion catalyst is heated by supplying hydrogen from the hydrogen storage device 11 that stores hydrogen in advance or from outside to the combustion catalyst chamber 3 via the pipe 10. Then, when the temperature of the combustion catalyst reaches 500° C. or higher, methane is gradually supplied through the pipe 4 to switch from hydrogen to methane. After the steam reforming reactor 1 reaches a predetermined temperature, raw material methane gas and raw material steam are supplied into the steam reforming reactor 1 from the raw material supply pipe 2 to stabilize the system. Then, when the load is low or the system is stopped, hydrogen is stored in the hydrogen storage device 11 for the next startup,
During other operations, the exhaust gas from the hydrogen electrode 7 is transferred to the bypass pipe 1.
2 to the combustion catalyst chamber 3.

【0015】ここで、本実施例における燃焼触媒室3内
の燃焼触媒層温度の経時変化を図2に示す。同図に示す
ように、本実施例では常温から水素を供給したが、約1
時間で水素からメタンに切り換えることができた。
FIG. 2 shows the change in temperature of the combustion catalyst layer in the combustion catalyst chamber 3 over time in this embodiment. As shown in the figure, in this example, hydrogen was supplied from room temperature, but approximately 1
It was possible to switch from hydrogen to methane in a matter of hours.

【0016】一方、従来においては、起動時にはメタン
ガスを原料としたバーナー加熱等により燃焼触媒層を昇
温し、その後の定常運転時には水素極7からの排ガスと
燃焼触媒室に導入して加熱していた。比較のため、かか
るバーナー加熱による起動時の経時変化を図3に示す。 同図に示すように、この場合、管壁の温度は輻射熱で急
激に850℃付近まで上昇したが、内部の燃焼触媒温度
の上昇は遅く、メタンが導入できるまで(約500℃と
なるまで)に約2時間必要であった。
On the other hand, conventionally, at startup, the temperature of the combustion catalyst layer is raised by heating with a burner using methane gas as a raw material, and then during steady operation, exhaust gas from the hydrogen electrode 7 is introduced into the combustion catalyst chamber to heat it. Ta. For comparison, FIG. 3 shows changes over time during startup due to such burner heating. As shown in the figure, in this case, the temperature of the tube wall rapidly rose to around 850°C due to radiant heat, but the internal combustion catalyst temperature rose slowly until methane could be introduced (until it reached about 500°C). It took about 2 hours.

【0017】[0017]

【発明の効果】以上説明したように、本発明方法によれ
ば、常温からの触媒燃焼が可能であり、局部加熱も防止
されるため、水蒸気改質反応器がコンパクトになると共
に材料コストが安価となる。また、燃焼触媒による起動
によるので、燃焼温度の制御が簡単で、バーナーに比べ
て安定性が高く、しかも、温度上昇が速くて起動時間が
短縮されるという効果を奏する。
[Effects of the Invention] As explained above, according to the method of the present invention, catalytic combustion is possible from room temperature and local heating is prevented, so the steam reforming reactor can be made more compact and the material cost can be reduced. becomes. In addition, since startup is performed by a combustion catalyst, the combustion temperature can be easily controlled, stability is higher than that of a burner, and the temperature rises quickly, resulting in a short startup time.

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

【図1】一実施例に係る燃料電池システムの構成図であ
る。
FIG. 1 is a configuration diagram of a fuel cell system according to one embodiment.

【図2】実施例における燃焼触媒温度の経時変化を示す
説明図である。
FIG. 2 is an explanatory diagram showing a change in combustion catalyst temperature over time in an example.

【図3】比較例に係る燃焼触媒温度の経時変化を示す説
明図である。
FIG. 3 is an explanatory diagram showing a change in combustion catalyst temperature over time according to a comparative example.

【符号の説明】[Explanation of symbols]

1  水蒸気改質反応器 3  燃焼触媒室 5  CO変成器 6  燃料電池 7  水素極 8  空気極 11  水素貯蔵器 12  バイパス配管 1 Steam reforming reactor 3 Combustion catalyst chamber 5 CO transformer 6 Fuel cell 7 Hydrogen electrode 8 Air electrode 11 Hydrogen storage device 12 Bypass piping

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】  触媒燃焼方式の水蒸気改質反応器にメ
タンやメタノール等の炭化水素や含酸素炭化水素からな
る原料を供給して水蒸気改質反応により水素濃度が高い
ガスを製造し、該製造ガスを固体高分子電解質型燃料電
池に供給して発電する燃料電池システムの起動に際し、
水素吸蔵合金を内蔵する水素貯蔵器から発生させた水素
を上記水蒸気改質反応器に供給して触媒燃料に使用する
ことを特徴とする燃料電池システムの起動方法。
Claim 1: Supplying a raw material consisting of hydrocarbons or oxygen-containing hydrocarbons such as methane or methanol to a catalytic combustion type steam reforming reactor to produce gas with a high hydrogen concentration through a steam reforming reaction; When starting up a fuel cell system that supplies gas to a solid polymer electrolyte fuel cell to generate electricity,
A method for starting a fuel cell system, comprising supplying hydrogen generated from a hydrogen storage device containing a hydrogen storage alloy to the steam reforming reactor and using it as a catalytic fuel.
JP3109068A 1991-05-14 1991-05-14 Method for starting fuel cell system Withdrawn JPH04338101A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3109068A JPH04338101A (en) 1991-05-14 1991-05-14 Method for starting fuel cell system

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3109068A JPH04338101A (en) 1991-05-14 1991-05-14 Method for starting fuel cell system

Publications (1)

Publication Number Publication Date
JPH04338101A true JPH04338101A (en) 1992-11-25

Family

ID=14500788

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3109068A Withdrawn JPH04338101A (en) 1991-05-14 1991-05-14 Method for starting fuel cell system

Country Status (1)

Country Link
JP (1) JPH04338101A (en)

Cited By (19)

* Cited by examiner, † Cited by third party
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US5527632A (en) * 1992-07-01 1996-06-18 Rolls-Royce And Associates Limited Hydrocarbon fuelled fuel cell power system
JP2000220805A (en) * 1998-11-09 2000-08-08 Nippon Soken Inc Catalytic combustion heating device
US6268075B1 (en) 1997-12-16 2001-07-31 Xcellsis Gmbh Process for the water vapor reforming of a hydrocarbon or a hydrocarbon derivative, reforming system operable thereby, and fuel cell operating process
US6294149B1 (en) 1997-12-16 2001-09-25 Xcellsis Gmbh Process for operating a water vapor reforming system, a reforming system operable thereby and a fuel cell system operating process
JP2002329517A (en) * 2001-05-01 2002-11-15 Honda Motor Co Ltd Warm-up device for reformer used in fuel cell system
US6494937B1 (en) 2001-09-27 2002-12-17 Idatech, Llc Hydrogen purification devices, components and fuel processing systems containing the same
WO2004014788A1 (en) * 2002-08-09 2004-02-19 Honda Giken Kogyo Kabushiki Kaisha Hydrogen generating apparatus
US6953497B2 (en) 2001-09-27 2005-10-11 Idatech, Llc Hydrogen purification devices, components and fuel processing systems containing the same
US7052530B2 (en) 1996-10-30 2006-05-30 Idatech, Llc Hydrogen purification membranes, components and fuel processing systems containing the same
US7195663B2 (en) 1996-10-30 2007-03-27 Idatech, Llc Hydrogen purification membranes, components and fuel processing systems containing the same
US7470293B2 (en) 2004-10-29 2008-12-30 Idatech, Llc Feedstock delivery systems, fuel processing systems, and hydrogen generation assemblies including the same
US7501456B2 (en) 2006-04-27 2009-03-10 Compactgtl Plc Process for preparing liquid hydrocarbons
JP2009217968A (en) * 2008-03-07 2009-09-24 Casio Comput Co Ltd Power generation apparatus, and electronic equipment
US7601302B2 (en) 2005-09-16 2009-10-13 Idatech, Llc Self-regulating feedstock delivery systems and hydrogen-generating fuel processing assemblies and fuel cell systems incorporating the same
US7629067B2 (en) 2006-05-22 2009-12-08 Idatech, Llc Hydrogen-producing fuel processing systems and fuel cell systems with a liquid leak detection system
US7632322B2 (en) 2005-06-07 2009-12-15 Idatech, Llc Hydrogen-producing fuel processing assemblies, heating assemblies, and methods of operating the same
US10476093B2 (en) 2016-04-15 2019-11-12 Chung-Hsin Electric & Machinery Mfg. Corp. Membrane modules for hydrogen separation and fuel processors and fuel cell systems including the same
US11316180B2 (en) 2020-05-21 2022-04-26 H2 Powertech, Llc Hydrogen-producing fuel cell systems and methods of operating hydrogen-producing fuel cell systems for backup power operations
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US7410531B2 (en) 1996-10-30 2008-08-12 Idatech, Llc Hydrogen purification membranes, components and fuel processing systems containing the same
US7195663B2 (en) 1996-10-30 2007-03-27 Idatech, Llc Hydrogen purification membranes, components and fuel processing systems containing the same
US6268075B1 (en) 1997-12-16 2001-07-31 Xcellsis Gmbh Process for the water vapor reforming of a hydrocarbon or a hydrocarbon derivative, reforming system operable thereby, and fuel cell operating process
US6294149B1 (en) 1997-12-16 2001-09-25 Xcellsis Gmbh Process for operating a water vapor reforming system, a reforming system operable thereby and a fuel cell system operating process
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US7632322B2 (en) 2005-06-07 2009-12-15 Idatech, Llc Hydrogen-producing fuel processing assemblies, heating assemblies, and methods of operating the same
US7601302B2 (en) 2005-09-16 2009-10-13 Idatech, Llc Self-regulating feedstock delivery systems and hydrogen-generating fuel processing assemblies and fuel cell systems incorporating the same
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US10476093B2 (en) 2016-04-15 2019-11-12 Chung-Hsin Electric & Machinery Mfg. Corp. Membrane modules for hydrogen separation and fuel processors and fuel cell systems including the same
US11316180B2 (en) 2020-05-21 2022-04-26 H2 Powertech, Llc Hydrogen-producing fuel cell systems and methods of operating hydrogen-producing fuel cell systems for backup power operations
US11831051B2 (en) 2020-05-21 2023-11-28 H2 Powertech, Llc Hydrogen-producing fuel cell systems and methods of operating hydrogen-producing fuel cell systems for backup power operations
US11712655B2 (en) 2020-11-30 2023-08-01 H2 Powertech, Llc Membrane-based hydrogen purifiers
US12226732B2 (en) 2020-11-30 2025-02-18 H2 Powertech, Llc Membrane-based hydrogen purifiers

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