JPS58219945A - Catalyst for reforming hydrocarbon - Google Patents
Catalyst for reforming hydrocarbonInfo
- Publication number
- JPS58219945A JPS58219945A JP57103226A JP10322682A JPS58219945A JP S58219945 A JPS58219945 A JP S58219945A JP 57103226 A JP57103226 A JP 57103226A JP 10322682 A JP10322682 A JP 10322682A JP S58219945 A JPS58219945 A JP S58219945A
- Authority
- JP
- Japan
- Prior art keywords
- catalyst
- reforming
- hydrocarbon
- inorg
- catalyst body
- 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
- 239000003054 catalyst Substances 0.000 title claims abstract description 51
- 229930195733 hydrocarbon Natural products 0.000 title claims abstract description 17
- 150000002430 hydrocarbons Chemical class 0.000 title claims abstract description 17
- 239000004215 Carbon black (E152) Substances 0.000 title claims abstract description 11
- 238000002407 reforming Methods 0.000 title claims abstract description 11
- 239000003779 heat-resistant material Substances 0.000 claims abstract 3
- 239000011148 porous material Substances 0.000 claims description 3
- 238000010438 heat treatment Methods 0.000 abstract description 11
- 238000006057 reforming reaction Methods 0.000 abstract description 8
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 abstract description 6
- 229910052751 metal Inorganic materials 0.000 abstract description 4
- 239000002184 metal Substances 0.000 abstract description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract description 3
- 229910002092 carbon dioxide Inorganic materials 0.000 abstract description 3
- 239000001569 carbon dioxide Substances 0.000 abstract description 3
- 239000007789 gas Substances 0.000 abstract description 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract description 3
- 239000001257 hydrogen Substances 0.000 abstract description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 3
- 229910052742 iron Inorganic materials 0.000 abstract description 2
- 229910052759 nickel Inorganic materials 0.000 abstract description 2
- 230000000977 initiatory effect Effects 0.000 abstract 1
- 238000000465 moulding Methods 0.000 abstract 1
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical group [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 abstract 1
- 239000000446 fuel Substances 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 230000004913 activation Effects 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000005611 electricity Effects 0.000 description 2
- 229910001872 inorganic gas Inorganic materials 0.000 description 2
- 239000011810 insulating material Substances 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000003570 air Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 238000002309 gasification Methods 0.000 description 1
- 230000017525 heat dissipation Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- -1 platinum group metals Chemical class 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J12/00—Chemical processes in general for reacting gaseous media with gaseous media; Apparatus specially adapted therefor
- B01J12/007—Chemical processes in general for reacting gaseous media with gaseous media; Apparatus specially adapted therefor in the presence of catalytically active bodies, e.g. porous plates
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J15/00—Chemical processes in general for reacting gaseous media with non-particulate solids, e.g. sheet material; Apparatus specially adapted therefor
- B01J15/005—Chemical processes in general for reacting gaseous media with non-particulate solids, e.g. sheet material; Apparatus specially adapted therefor in the presence of catalytically active bodies, e.g. porous plates
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physical Or Chemical Processes And Apparatus (AREA)
- Hydrogen, Water And Hydrids (AREA)
- Catalysts (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は炭化水素を水又は空気と混合しリフォーミング
触媒により、水素及び炭酸ガスを主体とした無機ガスに
改質する、比較的小形の炭化水素改質装置用触媒にかか
るものである。即ち、リフォーミング反応を開始するに
は、触媒を反応の活性開始温度迄予熱する必要があり、
本発明は、リフォーミング触媒の初期予熱方法を提供す
るものである。DETAILED DESCRIPTION OF THE INVENTION The present invention provides a catalyst for a relatively small hydrocarbon reformer that mixes hydrocarbons with water or air and uses a reforming catalyst to reform them into inorganic gases mainly consisting of hydrogen and carbon dioxide. This applies to That is, in order to start the reforming reaction, it is necessary to preheat the catalyst to the reaction activation temperature,
The present invention provides a method for initial preheating of a reforming catalyst.
′従来この種の触媒体の加熱方法は第3図、第4図に示
す如く、触媒体16周囲からヒータ16を用い加熱する
方法(第3図)と、燃料気流を予め触媒活性温度に迄加
熱する方法(第4図)とがあるが、いづれも相当の欠点
がある。'Conventionally, as shown in FIGS. 3 and 4, the conventional heating methods for this type of catalyst body include heating the catalyst body 16 from around it using a heater 16 (Figure 3), and heating the fuel air flow to the catalyst activation temperature in advance. There is a heating method (Fig. 4), but each method has considerable drawbacks.
即ち、外周より加熱する方法は、熱伝導に頼るため、触
媒体16全体を活性温度にまで高めるには相当の時間を
要し、かつ触媒体16自身の温度ムラも大きく均一な温
度分布となりにくい(ヒータ16に近い所は温度が高く
、遠い所は低い)。That is, the method of heating from the outer periphery relies on heat conduction, so it takes a considerable amount of time to raise the entire catalyst body 16 to the activation temperature, and the temperature unevenness of the catalyst body 16 itself is large, making it difficult to achieve a uniform temperature distribution. (The temperature is high in places close to the heater 16, and low in places far away).
特に多孔状の触媒体では空・隙が大きく、熱伝導が非常
に悪い。この為、均一温度に触媒体16を加熱すること
が出来ない。一方燃料気流を予熱する方法についても別
途に大容量の加熱装置17が必要であり、装置自身も大
型なものにならざるを得ない。In particular, porous catalyst bodies have large voids and gaps, resulting in very poor heat conduction. For this reason, the catalyst body 16 cannot be heated to a uniform temperature. On the other hand, the method of preheating the fuel airflow also requires a separate large-capacity heating device 17, and the device itself must be large-sized.
本発明は以上述べたような従来の諸欠点を除去するもの
で、触媒体1体を加熱させる事により、触媒体の加熱時
間を大巾に短縮させ、触媒体の加熱ムラを無くシ、さら
に加熱の、ためのエネルギーを大巾に削減させる事を目
的とするものである。The present invention eliminates the various drawbacks of the conventional methods as described above. By heating a single catalyst body, the heating time of the catalyst body can be greatly shortened, and uneven heating of the catalyst body can be eliminated. The purpose is to significantly reduce the energy required for heating.
この目的を達成するために本発明は多孔状の触媒体の孔
内に加熱用ヒータを設け、触媒体を内部から加熱するも
のである〇
この構成において、触媒体の孔内の加熱用ヒータに通電
することにより、触媒体そのものを簡単に加熱でき、そ
こに、燃料と水又は空気の混合物を供給することにより
、リフォーミング反応を開始させる。以後安定した状態
で反応を継続する。In order to achieve this object, the present invention provides a heater in the pores of a porous catalyst body to heat the catalyst body from the inside. In this configuration, the heater in the pores of the catalyst body By supplying electricity, the catalyst itself can be easily heated, and by supplying a mixture of fuel and water or air thereto, the reforming reaction is started. Thereafter, the reaction is continued in a stable state.
特にガス化材として空気を用いた部分酸化反応では、加
熱用ヒータに通電するのは燃焼初期のみで、リフォーミ
ング反応が継続しはじめると、通電する必要はない。Particularly in a partial oxidation reaction using air as a gasification agent, the heater is energized only during the initial stage of combustion, and once the reforming reaction begins to continue, there is no need to energize the heater.
以下本発明の一実施例を図面とともに説明する。An embodiment of the present invention will be described below with reference to the drawings.
第1図、第2図において、改質器1は2重管によって構
成され、内管2の内側にリフオーミング用触媒体3を有
する。また内管2の一端には燃料供給口4を設ける。一
方二重管の外管5の一端には、ガス排出口6を有する。In FIGS. 1 and 2, a reformer 1 is constituted by a double tube, and has a reforming catalyst body 3 inside an inner tube 2. As shown in FIG. Further, a fuel supply port 4 is provided at one end of the inner tube 2. On the other hand, a gas outlet 6 is provided at one end of the outer tube 5 of the double tube.
又、外管5の外周部には、断熱材7が巻きつけである。Further, a heat insulating material 7 is wrapped around the outer circumference of the outer tube 5.
一方燃料供給口4は、混合管8とつながっている。混合
管8は、空気供給管9、炭化水素供給管10を有する。On the other hand, the fuel supply port 4 is connected to the mixing pipe 8. The mixing pipe 8 has an air supply pipe 9 and a hydrocarbon supply pipe 10.
一方、改質器1の一端は、ボルト11により取り外し可
能となっている。触媒体3は、第2図A、Hに示す層の
薄壁からなる円筒型に一体成型した触媒担体12に、ニ
ッケル、コバルト、鉄、白金族等、リフォーミング反応
に活性をもつ金属を担持したものであり、触媒担体12
の孔13内に針金状の電気ヒータ14を通しである。On the other hand, one end of the reformer 1 can be removed with a bolt 11. The catalyst body 3 includes a catalyst carrier 12 integrally molded into a cylindrical shape made of thin walls of layers shown in FIGS. 2A and 2H, which supports metals active in reforming reactions, such as nickel, cobalt, iron, and platinum group metals. The catalyst carrier 12
A wire-shaped electric heater 14 is passed through the hole 13.
次に本作用について述べる。Next, this effect will be described.
予め所定の温度(600℃〜900℃)迄、リフォーミ
ング用の触媒体3中に通した針金状の電気ヒータ14に
通電し、リフォーミング用の触媒体3を加熱する。所定
温度に達した後、空気供給管9、炭化水素供給管10よ
り、それぞれ空気と、・炭化水素を供給する。供給され
た空気と炭化水素は混合管8で十分混合された後、燃料
供給口4より、改質器1内に供給される。さらに混合さ
れた空気と炭化水素は燃料供給口から内管2を通って、
触媒体3に供給される迄に予熱された後、触媒体3に接
し、リフォーミング反応を行う。反応の結果、生成され
・た水素、炭酸ガスを主体とした無機ガスは、二重管の
外管5を通り、内管2を通る炭化水素と空気の混合ガス
と熱交換を行いながら、ガス排出口6より排出され、そ
れぞれの用途に用いられる。さらに二重管の外管5の外
側の断熱材7は、熱の放散をふせぎ、熱の有効利用を図
っている。一方、反応の結果、劣化した触媒体3は、改
質器1の一端のポルト11をはずす事により、新しい触
媒体3と交換出来るようになっている。The wire-shaped electric heater 14 passed through the reforming catalyst body 3 is energized to heat the reforming catalyst body 3 to a predetermined temperature (600° C. to 900° C.). After reaching a predetermined temperature, air and hydrocarbons are supplied from the air supply pipe 9 and the hydrocarbon supply pipe 10, respectively. The supplied air and hydrocarbons are sufficiently mixed in the mixing pipe 8 and then supplied into the reformer 1 through the fuel supply port 4. Furthermore, the mixed air and hydrocarbons pass through the inner pipe 2 from the fuel supply port,
After being preheated before being supplied to the catalyst body 3, it comes into contact with the catalyst body 3 and undergoes a reforming reaction. As a result of the reaction, the inorganic gas mainly consisting of hydrogen and carbon dioxide passes through the outer tube 5 of the double tube and exchanges heat with the mixed gas of hydrocarbons and air passing through the inner tube 2. It is discharged from the discharge port 6 and used for each purpose. Furthermore, the heat insulating material 7 on the outside of the double-pipe outer tube 5 prevents heat dissipation and aims at effective use of heat. On the other hand, the catalyst body 3 that has deteriorated as a result of the reaction can be replaced with a new catalyst body 3 by removing the port 11 at one end of the reformer 1.
以上のような作用により、リフォーミング反応を継続す
るわけであるが、炭化水素と空気のみをガス化材として
用いた部分酸化反応では、触媒体3中の電気ヒータ14
に通電するのは、反応の初期のみで、後は、自然焼によ
り、反応を継続する事が出来る。The reforming reaction continues due to the above-mentioned action, but in a partial oxidation reaction using only hydrocarbons and air as gasifying materials, the electric heater 14 in the catalyst body 3
Electricity is applied only during the initial stage of the reaction, after which the reaction can be continued by natural firing.
次に本発明による炭化水素改質用触媒を用いた場合の効
果は次のようである。Next, the effects of using the hydrocarbon reforming catalyst according to the present invention are as follows.
(1)触媒体を所定の活性温度(60o〜eoo℃)に
まで上げるのに短時間しかかからない。(1) It takes only a short time to raise the catalyst to a predetermined activation temperature (60° to eoo°C).
(2)触媒体自身を加熱するため、余分なエネルギーの
消耗をなくす事が出来る。(2) Since the catalyst itself is heated, excess energy consumption can be eliminated.
(3)触媒体全体を均一に加熱する事が出来、温度ムラ
を無くすことが出来る。(3) The entire catalyst body can be heated uniformly, and temperature unevenness can be eliminated.
第1図は本発明の一実施例である炭化水素改質用触媒を
有する炭化水素燃料改質装置の断面図、第2図A、Bは
触媒体の正面図と断面図、第3図、第4図は従来例を示
す断面図である。
計・・・・・触媒体、12・・・・・・触媒担体、13
・・・・・・孔、14・・・・・・電気ヒータ。
代理人の氏名 弁理士 中 尾 敏 男 ほか1名第1
図
↑
・r″jX
第2図FIG. 1 is a sectional view of a hydrocarbon fuel reformer having a hydrocarbon reforming catalyst according to an embodiment of the present invention, FIGS. 2A and B are a front view and a sectional view of a catalyst body, and FIG. FIG. 4 is a sectional view showing a conventional example. Total...Catalyst body, 12...Catalyst carrier, 13
...hole, 14...electric heater. Name of agent: Patent attorney Toshio Nakao and 1 other person No. 1
Figure ↑ ・r″jX Figure 2
Claims (1)
体の孔内に加熱用ヒータを設けた炭化水素改質用触媒。A hydrocarbon reforming catalyst comprising a porous catalyst body made of an inorganic heat-resistant material and a heater provided in the pores of the catalyst body.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57103226A JPS58219945A (en) | 1982-06-15 | 1982-06-15 | Catalyst for reforming hydrocarbon |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57103226A JPS58219945A (en) | 1982-06-15 | 1982-06-15 | Catalyst for reforming hydrocarbon |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS58219945A true JPS58219945A (en) | 1983-12-21 |
Family
ID=14348560
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP57103226A Pending JPS58219945A (en) | 1982-06-15 | 1982-06-15 | Catalyst for reforming hydrocarbon |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS58219945A (en) |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1994019098A1 (en) * | 1993-02-24 | 1994-09-01 | Serthel | Thermal reactor with direct passage tube for current |
EP0913357A1 (en) * | 1997-10-28 | 1999-05-06 | Ngk Insulators, Ltd. | Reformer and method for operation thereof |
EP0967174A1 (en) * | 1998-06-29 | 1999-12-29 | Ngk Insulators, Ltd. | Reformer |
US6187066B1 (en) | 1996-09-24 | 2001-02-13 | Daimlerchrysler Ag | Central heating device for a gas-generating system |
US6390030B1 (en) | 1999-06-03 | 2002-05-21 | Toyota Jidosha Kabushiki Kaisha | Fuel reformer for mounting on a vehicle |
JP2002293503A (en) * | 2001-03-30 | 2002-10-09 | Ishikawajima Harima Heavy Ind Co Ltd | Reformer |
US6692707B1 (en) | 1999-03-03 | 2004-02-17 | Toyota Jidosha Kabushiki Kaisha | Hydrocarbon fuel reformer |
JP2007057110A (en) * | 2005-08-22 | 2007-03-08 | Alumite Shokubai Kenkyusho:Kk | Catalytic combustion apparatus |
JP2007175612A (en) * | 2005-12-27 | 2007-07-12 | Central Res Inst Of Electric Power Ind | Decomposition and removal apparatus and decomposition and removal method using same |
JP2009203136A (en) * | 2008-02-28 | 2009-09-10 | Kyocera Corp | Reaction apparatus |
WO2022093363A1 (en) * | 2020-10-30 | 2022-05-05 | Gas Technology Institute | Electrically heated reforming reactor for reforming of methane and other hydrocarbons |
-
1982
- 1982-06-15 JP JP57103226A patent/JPS58219945A/en active Pending
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2701863A1 (en) * | 1993-02-24 | 1994-09-02 | Serthel | Thermal reactor with direct flow tube. |
WO1994019098A1 (en) * | 1993-02-24 | 1994-09-01 | Serthel | Thermal reactor with direct passage tube for current |
US6187066B1 (en) | 1996-09-24 | 2001-02-13 | Daimlerchrysler Ag | Central heating device for a gas-generating system |
EP0913357A1 (en) * | 1997-10-28 | 1999-05-06 | Ngk Insulators, Ltd. | Reformer and method for operation thereof |
US6641795B2 (en) | 1997-10-28 | 2003-11-04 | Ngk Insulators, Ltd. | Reformer and method for operation thereof |
EP0967174A1 (en) * | 1998-06-29 | 1999-12-29 | Ngk Insulators, Ltd. | Reformer |
US6692707B1 (en) | 1999-03-03 | 2004-02-17 | Toyota Jidosha Kabushiki Kaisha | Hydrocarbon fuel reformer |
US6390030B1 (en) | 1999-06-03 | 2002-05-21 | Toyota Jidosha Kabushiki Kaisha | Fuel reformer for mounting on a vehicle |
JP2002293503A (en) * | 2001-03-30 | 2002-10-09 | Ishikawajima Harima Heavy Ind Co Ltd | Reformer |
JP4590766B2 (en) * | 2001-03-30 | 2010-12-01 | 株式会社Ihi | Reformer |
JP2007057110A (en) * | 2005-08-22 | 2007-03-08 | Alumite Shokubai Kenkyusho:Kk | Catalytic combustion apparatus |
JP4534154B2 (en) * | 2005-08-22 | 2010-09-01 | 株式会社 アルマイト触媒研究所 | Catalytic combustion device |
JP2007175612A (en) * | 2005-12-27 | 2007-07-12 | Central Res Inst Of Electric Power Ind | Decomposition and removal apparatus and decomposition and removal method using same |
JP2009203136A (en) * | 2008-02-28 | 2009-09-10 | Kyocera Corp | Reaction apparatus |
WO2022093363A1 (en) * | 2020-10-30 | 2022-05-05 | Gas Technology Institute | Electrically heated reforming reactor for reforming of methane and other hydrocarbons |
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