JPH01203201A - Method for thermally decomposing gaseous hydrocarbon at high temperature - Google Patents
Method for thermally decomposing gaseous hydrocarbon at high temperatureInfo
- Publication number
- JPH01203201A JPH01203201A JP63026548A JP2654888A JPH01203201A JP H01203201 A JPH01203201 A JP H01203201A JP 63026548 A JP63026548 A JP 63026548A JP 2654888 A JP2654888 A JP 2654888A JP H01203201 A JPH01203201 A JP H01203201A
- Authority
- JP
- Japan
- Prior art keywords
- activated carbon
- filler
- carbon
- gaseous hydrocarbon
- high temperature
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B3/00—Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen; Reversible storage of hydrogen
- C01B3/02—Production of hydrogen; Production of gaseous mixtures containing hydrogen
- C01B3/04—Production of hydrogen; Production of gaseous mixtures containing hydrogen by decomposition of inorganic compounds
-
- 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
- Y02E60/36—Hydrogen production from non-carbon containing sources, e.g. by water electrolysis
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Combustion & Propulsion (AREA)
- Inorganic Chemistry (AREA)
- Hydrogen, Water And Hydrids (AREA)
- Catalysts (AREA)
Abstract
Description
【発明の詳細な説明】
〔従来の技術〕
従来のサバチエ反応によシ炭酸ガスを水素によって還元
し、生成したメタンガスを高温下で熱分解して水素と炭
素に変換する工程を第4図によって説明する。[Detailed Description of the Invention] [Prior Art] The process of reducing carbon dioxide gas with hydrogen through the conventional Sabatier reaction and thermally decomposing the generated methane gas at high temperatures to convert it into hydrogen and carbon is shown in Fig. 4. explain.
水素を混合され九次酸ガスは、鉄線[7が充填され、ヒ
ータ4で加熱されるサバチエ第1反応器2を通され、生
成する水をコンデンサ5で除去された後、メタンガスは
シリカウール6が充填され、ヒータ3で加熱されるサバ
チエ第2反応器1を通されて、水素と炭素に分解される
。The 9th acid gas mixed with hydrogen is passed through the Sabatier first reactor 2, which is filled with iron wire [7] and heated with a heater 4. After the produced water is removed with a condenser 5, the methane gas is passed through a silica wool 6. is charged and passed through the second Sabatier reactor 1 heated by a heater 3, where it is decomposed into hydrogen and carbon.
こ−においてメタンガスをサバチエ第2反露器1中にグ
ラスウール6を充填する理由は、シリカラブル6の繊維
表面の触媒作用と、メタンガスの分解によって生成する
炭素の担持作用を行わせるためで、該反応器1中に何ん
ら充填物を充填しない場合に比べて、メタンガスの分解
反応速度を著しく高め、かつ水素から炭素の分離が極め
て容易に行なえるものである。In this case, the reason why the glass wool 6 is filled into the Sabatier second dew reactor 1 for methane gas is to perform the catalytic action on the fiber surface of the silica rubble 6 and the supporting action of the carbon produced by the decomposition of the methane gas. Compared to the case where no filler is filled in the vessel 1, the decomposition reaction rate of methane gas is significantly increased, and carbon can be separated from hydrogen extremely easily.
メタンガスを水素と炭素に分解させるサバチエ第2反応
において、反応温度が高い程、熱分解効率は高くなるが
、高温になると電力消費が大きくなるので極端に温度を
上げることは実用上問題があ夛、省エネルギの点より低
温で熱分解効率を上げる工夫をすることが必要である。In Sabatier's second reaction, which decomposes methane gas into hydrogen and carbon, the higher the reaction temperature, the higher the thermal decomposition efficiency, but as the temperature increases, power consumption increases, so raising the temperature extremely poses many practical problems. From the point of view of energy conservation, it is necessary to devise ways to increase the thermal decomposition efficiency at low temperatures.
また、メタンのよう々炭化水素ガスの熱分解は大部分が
、充填材表面で起きると考えられ、このため充填材とし
ては表面積の大きなファイバ状のものが望まれている。Furthermore, most of the thermal decomposition of hydrocarbon gases such as methane is thought to occur on the surface of the filler, and for this reason, fillers in the form of fibers with a large surface area are desired.
従来、この充填材としてシリカウールを用いていたが、
これよυも更に表面積の大きい充填材が要望されている
。Traditionally, silica wool was used as this filler, but
There is a demand for a filler with an even larger surface area.
また、この熱分解反応は化学反応であるので充填材に触
媒作用があることが望まれているが、シリカウールには
触媒作用がなく、との要望に答えられない。Furthermore, since this thermal decomposition reaction is a chemical reaction, it is desired that the filler has a catalytic effect, but silica wool does not have a catalytic effect, which cannot meet the demand.
更に、また熱分解によって生じた炭素は充填材表面に析
出するが、充填材がシリカウールであると析出付着した
炭素を容易に分離することができず、したがって充填材
の再生が不可能という問題があった。Furthermore, carbon generated by thermal decomposition precipitates on the surface of the filler, but if the filler is silica wool, the precipitated carbon cannot be easily separated, making it impossible to regenerate the filler. was there.
本発明は上記技術水準に鑑み、従来のシリカウールより
も表面積が大で、かつ触媒作用を有し、再生可能な充填
材を用いてメタンなどの炭化水素ガスを水素と炭素に熱
分解する方法を提供しようとするものである。In view of the above-mentioned state of the art, the present invention provides a method for thermally decomposing hydrocarbon gas such as methane into hydrogen and carbon using a renewable filler that has a larger surface area than conventional silica wool, has a catalytic action, and is renewable. This is what we are trying to provide.
本発明は高温熱分解反応器の充填材として繊維状活性炭
を用いることを特徴とする炭化水素ガスの高温熱分解法
である。The present invention is a high-temperature pyrolysis method for hydrocarbon gas characterized by using fibrous activated carbon as a filler in a high-temperature pyrolysis reactor.
本発明で充填材として使用する充填材である繊維状活性
炭は、シリカウールよりも表面積が著しく高く(例えば
150 m”/ ’lにも及ぶ)、しかも表面は活性化
されているために細孔を有し、炭化水素ガスの熱分)]
イ反応の触媒としての作用をなす。また繊維状活性炭に
炭素が析出1〜でも、同じ炭素であるので再賦活に再利
用ができるばかりでなく、焼却あるいは粉砕して他用途
に再利用できる。Fibrous activated carbon, which is the filler used as a filler in the present invention, has a significantly higher surface area than silica wool (for example, as much as 150 m"/'l), and because the surface is activated, it has fewer pores. heat content of hydrocarbon gas)]
Acts as a catalyst for the reaction. Furthermore, even if carbon is precipitated in the fibrous activated carbon, it is the same carbon and can not only be reused for reactivation, but also be incinerated or pulverized and reused for other purposes.
繊維状活性炭として使用可能な形状としては、フィバ−
状、フェルト状のものがあげられる。The shape that can be used as fibrous activated carbon is fibrous activated carbon.
It can be felt-like or felt-like.
以下、本発明の一実施例を第1図によって説明する。第
1図の基本的フローは第4図と同一であり、第4図と同
一部分には同一符号を付しである。第1図において第4
図と異なるのは、サバチエ第2反応器1に充填されてい
る充填材がシリカラー−/ではなく繊維状活性炭である
ことである。、8はその繊維状活性炭を示す。An embodiment of the present invention will be described below with reference to FIG. The basic flow of FIG. 1 is the same as that of FIG. 4, and the same parts as in FIG. 4 are given the same reference numerals. 4 in Figure 1
What differs from the figure is that the filler packed in the Sabatier second reactor 1 is fibrous activated carbon rather than silica. , 8 indicates the fibrous activated carbon.
第1図のフローと第4図のフロ・−とを対比した結果の
うち、サバチエ第2反応器1における反応温度(’C)
と反応速度(kg c■(JH)の関係を第2図に示す
。この第2図から同一温度で本発明実施例の方が従来法
より反応速度が高くなっていることが判る。Among the results of comparing the flow in Figure 1 and the flow in Figure 4, the reaction temperature ('C) in Sabatier 2nd reactor 1
The relationship between and reaction rate (kg c (JH)) is shown in Figure 2. From Figure 2, it can be seen that at the same temperature, the reaction rate of the example of the present invention is higher than that of the conventional method.
また、同様にメタンガスの通気時間(E()と圧損(m
Aq )の関係を第5図に示す。この第3図から充填材
の充填量を同一にし、通気ガス流速を同一にした場合、
同じ圧損になるまでに本発明実施例の方がより多量のメ
タンガスを通気することができることが判る。Similarly, the ventilation time (E()) and pressure drop (m
Aq) is shown in FIG. From this figure 3, when the filling amount of the filler is the same and the ventilation gas flow rate is the same,
It can be seen that the embodiment of the present invention allows a larger amount of methane gas to be vented until the pressure drop is the same.
これ以外に、繊維状活性炭はシリカウールよシ、多量の
析出炭素を担持することができることも確認した。In addition to this, it was also confirmed that fibrous activated carbon can support a larger amount of precipitated carbon than silica wool.
本発明により炭化水素ガスの熱分解をよシ低温で実施す
ることができるようになった。The present invention has made it possible to carry out thermal decomposition of hydrocarbon gases at much lower temperatures.
第1図は本発明の一実施例のフローを示す概略図、第2
図、第5図は本発明の効果を従来法と対比して示す図表
、第4図は従来の炭化水素ガスの熱分解法のツーローの
概略図である。
第1國
第2図
反 応 温 度 (0C)FIG. 1 is a schematic diagram showing the flow of one embodiment of the present invention, and FIG.
5 is a chart showing the effects of the present invention in comparison with the conventional method, and FIG. 4 is a two-row schematic diagram of the conventional thermal decomposition method for hydrocarbon gas. Country 1 Figure 2 Reaction temperature (0C)
Claims (1)
ことを特徴とする炭化水素ガスの高温熱分解法。A high-temperature pyrolysis method for hydrocarbon gas characterized by using fibrous activated carbon as a filler in a high-temperature pyrolysis reactor.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63026548A JPH01203201A (en) | 1988-02-09 | 1988-02-09 | Method for thermally decomposing gaseous hydrocarbon at high temperature |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63026548A JPH01203201A (en) | 1988-02-09 | 1988-02-09 | Method for thermally decomposing gaseous hydrocarbon at high temperature |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH01203201A true JPH01203201A (en) | 1989-08-16 |
Family
ID=12196567
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63026548A Pending JPH01203201A (en) | 1988-02-09 | 1988-02-09 | Method for thermally decomposing gaseous hydrocarbon at high temperature |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH01203201A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH08165101A (en) * | 1994-12-14 | 1996-06-25 | Agency Of Ind Science & Technol | Production of hydrogen |
| JP2005058908A (en) * | 2003-08-12 | 2005-03-10 | Japan Steel Works Ltd:The | Lower hydrocarbon direct cracking catalyst, lower hydrocarbon direct cracking reactor, and lower hydrocarbon direct cracking reactor |
-
1988
- 1988-02-09 JP JP63026548A patent/JPH01203201A/en active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH08165101A (en) * | 1994-12-14 | 1996-06-25 | Agency Of Ind Science & Technol | Production of hydrogen |
| JP2005058908A (en) * | 2003-08-12 | 2005-03-10 | Japan Steel Works Ltd:The | Lower hydrocarbon direct cracking catalyst, lower hydrocarbon direct cracking reactor, and lower hydrocarbon direct cracking reactor |
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