JPH03275501A - Fuel reformer - Google Patents
Fuel reformerInfo
- Publication number
- JPH03275501A JPH03275501A JP2076204A JP7620490A JPH03275501A JP H03275501 A JPH03275501 A JP H03275501A JP 2076204 A JP2076204 A JP 2076204A JP 7620490 A JP7620490 A JP 7620490A JP H03275501 A JPH03275501 A JP H03275501A
- Authority
- JP
- Japan
- Prior art keywords
- reforming
- catalyst
- catalyst layer
- raw material
- bed
- 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
- 239000000446 fuel Substances 0.000 title claims description 16
- 239000003054 catalyst Substances 0.000 claims abstract description 93
- 238000002407 reforming Methods 0.000 claims abstract description 74
- 239000007789 gas Substances 0.000 claims abstract description 22
- 239000002994 raw material Substances 0.000 claims abstract description 19
- 239000001257 hydrogen Substances 0.000 claims abstract description 9
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 9
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 5
- 239000002245 particle Substances 0.000 claims description 21
- 238000010438 heat treatment Methods 0.000 claims description 3
- 239000000567 combustion gas Substances 0.000 abstract description 4
- 239000000463 material Substances 0.000 description 8
- 238000005192 partition Methods 0.000 description 6
- 150000002431 hydrogen Chemical class 0.000 description 4
- 238000002485 combustion reaction Methods 0.000 description 3
- 239000012530 fluid Substances 0.000 description 2
- 239000002737 fuel gas Substances 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000004080 punching Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003546 flue gas Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 239000012254 powdered material Substances 0.000 description 1
- 238000006057 reforming reaction Methods 0.000 description 1
- 230000035939 shock Effects 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
- H01M8/0631—Reactor construction specially adapted for combination reactor/fuel cell
-
- 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
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、改質原料を改質触媒の下に水素に冨むガスに
改質する燃料改質器に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a fuel reformer for reforming a reforming raw material into a hydrogen-rich gas under a reforming catalyst.
燃料改質器は原燃料ガスに水蒸気を付加してなる改質原
料を粒状の改質触媒が充填された改質管に通流し、この
改質管を熱媒体により加熱して改質原料を水素に冨むガ
スに改質するものであり、第2図に示すものが知られて
いる。In a fuel reformer, a reforming material made by adding water vapor to raw fuel gas is passed through a reforming tube filled with granular reforming catalyst, and the reforming tube is heated by a heat medium to convert the reforming material. It is used to reform gas into a gas rich in hydrogen, and the one shown in Fig. 2 is known.
第2図において改質管lは二重管構造であり、直立する
仕切円筒2の内外に設けられた内管3と外管4とが環状
の底板5で持続されて構成されている。なお仕切円筒2
は底板5から離して設けられている。In FIG. 2, the reforming tube 1 has a double tube structure, and is composed of an inner tube 3 and an outer tube 4 provided inside and outside of an upright partition cylinder 2, which are supported by an annular bottom plate 5. Furthermore, partition cylinder 2
is provided apart from the bottom plate 5.
改質管1には均一な粒径の改質触媒6が充填されて円管
3と仕切円筒2との間及び仕切円筒2と外管4との間は
それぞれ内触媒層7と外触媒層8とを形成し、内触媒層
7と外触媒層8とは下端で接続し、連続した触媒層を形
成している。なおlOは内触媒層7に改質原料を供給す
る改質原料入口、11は外触媒層8から排出される改質
ガスを送出する改質ガス出口である。The reforming tube 1 is filled with a reforming catalyst 6 having a uniform particle size, and an inner catalyst layer 7 and an outer catalyst layer are formed between the circular tube 3 and the partition cylinder 2 and between the partition cylinder 2 and the outer tube 4, respectively. 8, and the inner catalyst layer 7 and the outer catalyst layer 8 are connected at their lower ends to form a continuous catalyst layer. Note that lO is a reformed raw material inlet for supplying the reformed raw material to the inner catalyst layer 7, and 11 is a reformed gas outlet for delivering the reformed gas discharged from the outer catalyst layer 8.
改質管lの内管3の内部の上部にはバーナ12が設けら
れ、また改質管1の外管4を囲んで炉容器13が設けら
れ、その上部にバーナ12での燃焼により生じる燃焼ガ
スを排出する燃焼排ガス出口14が設けられている。A burner 12 is provided inside the inner tube 3 of the reforming tube 1, and a furnace vessel 13 is provided surrounding the outer tube 4 of the reforming tube 1. A flue gas outlet 14 is provided for discharging the gas.
このような構造によりバーナ12で燃料、例えば燃料電
池から排出される残存水素を含むオフガスを燃焼空気と
混合して燃焼させると火炎や燃焼ガスが生じ、燃焼ガス
は矢印の方向に内管3内を流れ、さらに改質管1の下端
で折返して外管4と炉容器13との間を流れて改質管l
内の内触媒層7と外触媒層8とからなる触媒層を加熱し
た後、燃焼排ガス出口14から排出される。一方、改質
原料人口10から改質原料を流入させ内触媒層7ム二流
入させると、内触媒層7から外触媒層8に流れ、バーナ
12からの火炎や燃焼ガスにより加熱されて改質原料は
水素に冨むガスに改質され、この改質された改質ガスは
改質ガス出口桝から外部、例えば燃料電池に供給される
。With this structure, when the burner 12 burns fuel, for example off-gas containing residual hydrogen discharged from a fuel cell, mixed with combustion air, a flame and combustion gas are generated, and the combustion gas flows into the inner pipe 3 in the direction of the arrow. , then turns back at the lower end of the reforming tube 1 and flows between the outer tube 4 and the furnace vessel 13 to form the reforming tube l.
After heating the catalyst layer consisting of the inner catalyst layer 7 and the outer catalyst layer 8, the combustion exhaust gas is discharged from the combustion exhaust gas outlet 14. On the other hand, when the reforming material flows in from the reforming material population 10 and flows into the inner catalyst layer 7, it flows from the inner catalyst layer 7 to the outer catalyst layer 8, is heated by the flame and combustion gas from the burner 12, and is reformed. The raw material is reformed into a gas rich in hydrogen, and the reformed gas is supplied to the outside, for example, a fuel cell, from a reformed gas outlet.
上記のような改質管内の触媒層は一種類の粒径の改質触
媒で形成され、この触媒層に改質原料を通流し、触媒層
を熱媒体により加熱して改質反応を行なって改質原料を
水素に冨むガスに改質している。このような燃料改質器
の頻繁な起動、停止や負荷変動を伴う長時間の運転を行
なうと、触媒粒自身のヒートショックや触媒層を形成す
る金属材料からなる改質管の熱による膨張、収縮による
機械的作用により触媒粒の粉化が生じる。そして粉化し
たものが下方に落下して触媒層の下部に堆積し、このた
め触媒層の流体抵抗が増加する原因になっていた。この
触媒層の流体抵抗の増加は触媒層を流れる改質原料の圧
力損失が増加することであり、このため投入される改質
原料が減少し、必要な改質ガス量を確保できないという
問題がある。The catalyst layer in the reforming tube as described above is formed of a reforming catalyst of one type of particle size, and the reforming raw material is passed through this catalyst layer, and the catalyst layer is heated by a heat medium to perform a reforming reaction. The raw material is reformed into hydrogen-rich gas. If such a fuel reformer is operated for a long period of time with frequent starting and stopping and load fluctuations, heat shock of the catalyst particles themselves, thermal expansion of the reforming tube made of the metal material that forms the catalyst layer, The mechanical action of shrinkage causes powdering of the catalyst particles. The powdered material then falls downward and accumulates at the bottom of the catalyst layer, causing an increase in the fluid resistance of the catalyst layer. This increase in fluid resistance in the catalyst layer means an increase in the pressure loss of the reforming material flowing through the catalyst bed, which results in a decrease in the amount of reforming material being input, leading to the problem of not being able to secure the required amount of reformed gas. be.
本発明の目的は、触媒層の改質触媒が粉化しても改質原
料が触媒層を流れる際の圧力損失の増加を防ぐことので
きる燃料改質器を提供することである。An object of the present invention is to provide a fuel reformer that can prevent an increase in pressure loss when a reforming raw material flows through the catalyst layer even if the reforming catalyst in the catalyst layer is powdered.
(課題を解決するための手段〕
上記iiuを解決するために、本発明によれば粒状の改
質触媒が充填されてなる触媒層を有する直立する改質管
を熱媒体により加熱し、改質管を通流する改質原料を水
素に冨むガスに改質する燃料改質器において、異なる二
種類の粒径のうち、粒径の大きい改質触媒からなる触媒
層を下部に、方粒径の小さい改質触媒からなる触媒層を
上部に分割して改質管内に配設するものとする。(Means for Solving the Problems) In order to solve the above-mentioned iiiu, according to the present invention, an upright reforming tube having a catalyst layer filled with a granular reforming catalyst is heated by a heating medium, In a fuel reformer that reforms the reforming raw material flowing through a pipe into gas rich in hydrogen, a catalyst layer consisting of a reforming catalyst with a larger particle size out of two different particle sizes is placed at the bottom, A catalyst layer consisting of a reforming catalyst with a small diameter is divided into an upper part and disposed inside the reforming tube.
(作 用)
改質管内の触媒層は粒径の大きい改質触媒からなる触媒
層を下部に、一方粒径の小さい改質触媒からなる触媒層
を上部に分割して形成している。(Function) The catalyst layer in the reforming tube is divided into a lower catalyst layer consisting of a reforming catalyst with a large particle size, and an upper catalyst layer consisting of a reforming catalyst with a small particle size.
したがって改質触媒が粉化して、この粉化した改質触媒
が下方に落下して下部の触媒層に堆積しても下部の触媒
層の改質触媒は粒径が大きいので、改質触媒間の空隙率
が大きく、このため改質原料の流路となる空隙は確保さ
れ、改質原料が触媒層を流れる際の圧力損失の増加を防
ぐ。Therefore, even if the reforming catalyst is powdered and this powdered reforming catalyst falls downward and deposits on the lower catalyst layer, the reforming catalyst in the lower catalyst layer has a large particle size, so there is no space between the reforming catalysts. The porosity of the catalyst layer is large, and therefore the voids that serve as flow paths for the reforming raw material are secured, thereby preventing an increase in pressure loss when the reforming raw material flows through the catalyst layer.
(実施例〕 以上図面に基づいて本発明の実施例について説明する。(Example〕 Embodiments of the present invention will be described above based on the drawings.
第1図は本発明の実施例による燃料改質器の断面図であ
る。なお、第1図において第2図の従来例と同一部品に
は同じ符号を付し、その説明を省略する。第1図におい
て第2図の従来例と異なって改質管lには異なる二種類
の粒径の改質触媒のうち、仕切板2の下端から下部に粒
径の大きい改質触媒20を充填して下部触媒層21を形
成し、上部C二粒径の小さい改質触媒22を充填してな
る上部触媒層23を形成している。なお、下部触媒層2
1と上部触媒層23とを分割するために仕切りとして粒
径の小さい改質触媒22が落ちない程度の孔を多数有す
るパンチングメタル24を挿入している。FIG. 1 is a sectional view of a fuel reformer according to an embodiment of the present invention. In FIG. 1, parts that are the same as those in the conventional example shown in FIG. 2 are given the same reference numerals, and their explanations will be omitted. In FIG. 1, unlike the conventional example shown in FIG. 2, the reforming tube l is filled with a reforming catalyst 20 having a larger particle size from the lower end of the partition plate 2, out of two types of reforming catalysts with different particle sizes. Then, a lower catalyst layer 21 is formed, and an upper catalyst layer 23 is formed, which is filled with reforming catalyst 22 having a small particle size. Note that the lower catalyst layer 2
1 and the upper catalyst layer 23, a punching metal 24 having a large number of holes to prevent the reforming catalyst 22 having a small particle size from falling is inserted as a partition.
このような構造により、改質触媒が粉化して粉化した改
質触媒が下方に落下し、パンチングメタル24の孔を通
って下部触媒層21に堆積しても、下部触媒層21の改
質触媒20は粒径が大きいので空隙率が大きいため、改
質原料が通流する流路となる空隙は確保される。したが
って、改質原料が改質原料人口10から上部、下部触媒
層23.21とからなる触媒層を通流して改質ガスとな
って改質ガス出口11から排出するときの圧力損失の増
加を防ぐことができる。With such a structure, even if the reforming catalyst is pulverized and the powdered reforming catalyst falls downward and is deposited on the lower catalyst layer 21 through the holes of the punching metal 24, the reforming of the lower catalyst layer 21 is prevented. Since the catalyst 20 has a large particle size and a large porosity, voids that serve as channels through which the reforming raw material flows are secured. Therefore, the pressure loss increases when the reformed raw material flows from the reformed raw material population 10 through the catalyst layer consisting of the upper and lower catalyst layers 23 and 21 to become reformed gas and is discharged from the reformed gas outlet 11. It can be prevented.
以上の説明から明らかなように、本発明によれば改質管
内にその下部に粒径の大きい改質触媒からなる触媒層と
、この上部に粒径の小さい改質触媒からなる触媒層とを
分割して形成したことにより、燃料改質器の頻繁な起動
、停止や負荷変動を伴う長期運転により改質触媒が粉化
し、粉化した改質触媒は下方に落下して下部の触媒層に
堆積しても、この触媒層の改質触媒の粒径が大きく空隙
率が大きいため、原燃料ガスに水蒸気を付加してなる改
質原料が通流する流路は確保され、したがって改質原料
の触媒層を流れる圧力損失の増加を防止し、外部負荷が
要求する改質ガス量、例えば燃料電池の負荷が要求する
改質ガス量を住成できる。As is clear from the above description, according to the present invention, a catalyst layer consisting of a reforming catalyst with a large particle size is provided in the lower part of the reforming tube, and a catalyst layer consisting of a reforming catalyst with a small particle size is provided in the upper part of the reforming tube. By forming the catalyst separately, the reforming catalyst becomes powdered due to long-term operation with frequent starting and stopping of the fuel reformer and load fluctuations, and the powdered reforming catalyst falls downward to the lower catalyst layer. Even if it accumulates, the particle size of the reforming catalyst in this catalyst layer is large and the porosity is large, so a flow path is secured through which the reforming material made by adding water vapor to the raw fuel gas flows, and therefore the reforming material The amount of reformed gas required by the external load, for example, the amount of reformed gas required by the load of the fuel cell, can be achieved.
第1図は本発明の実施例による燃料改質器の断面図、第
2図は従来の燃料改質器の断面図である。
1:改質管、20:粒径の大きい改質触媒、22:第1
図FIG. 1 is a sectional view of a fuel reformer according to an embodiment of the present invention, and FIG. 2 is a sectional view of a conventional fuel reformer. 1: Reforming pipe, 20: Reforming catalyst with large particle size, 22: First
figure
Claims (1)
立する改質管を熱媒体により加熱し、改質管を通流する
改質原料を水素に富むガスに改質する燃料改質器におい
て、異なる二種類の粒径のうち、粒径の大きい改質触媒
からなる触媒層を下部に、一方粒径の小さい改質触媒か
らなる触媒層を上部に分割して改質管内に配設したこと
を特徴とする燃料改質器。1) Fuel reforming in which an upright reforming tube having a catalyst layer filled with granular reforming catalyst is heated by a heating medium to reform the reforming raw material flowing through the reforming tube into hydrogen-rich gas. In the reformer, the catalyst layer consisting of the reforming catalyst with the larger particle size is placed in the lower part of the two different particle sizes, and the catalyst layer consisting of the reforming catalyst with the smaller particle size is placed in the upper part. A fuel reformer characterized by:
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2076204A JPH03275501A (en) | 1990-03-26 | 1990-03-26 | Fuel reformer |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2076204A JPH03275501A (en) | 1990-03-26 | 1990-03-26 | Fuel reformer |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03275501A true JPH03275501A (en) | 1991-12-06 |
Family
ID=13598631
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2076204A Pending JPH03275501A (en) | 1990-03-26 | 1990-03-26 | Fuel reformer |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03275501A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006054171A (en) * | 2004-07-12 | 2006-02-23 | Osaka Gas Co Ltd | Solid oxide fuel cell system |
KR20190025381A (en) * | 2017-09-01 | 2019-03-11 | 엘지전자 주식회사 | Fuel reforming divice |
-
1990
- 1990-03-26 JP JP2076204A patent/JPH03275501A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006054171A (en) * | 2004-07-12 | 2006-02-23 | Osaka Gas Co Ltd | Solid oxide fuel cell system |
KR20190025381A (en) * | 2017-09-01 | 2019-03-11 | 엘지전자 주식회사 | Fuel reforming divice |
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