JPH0418009B2 - - Google Patents
Info
- Publication number
- JPH0418009B2 JPH0418009B2 JP59003228A JP322884A JPH0418009B2 JP H0418009 B2 JPH0418009 B2 JP H0418009B2 JP 59003228 A JP59003228 A JP 59003228A JP 322884 A JP322884 A JP 322884A JP H0418009 B2 JPH0418009 B2 JP H0418009B2
- Authority
- JP
- Japan
- Prior art keywords
- air
- butane
- gas
- retort
- catalyst
- 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.)
- Expired - Lifetime
Links
- 239000001273 butane Substances 0.000 claims description 27
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 claims description 27
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims description 27
- 239000003054 catalyst Substances 0.000 claims description 24
- 238000010438 heat treatment Methods 0.000 claims description 24
- 229930195733 hydrocarbon Natural products 0.000 claims description 21
- 150000002430 hydrocarbons Chemical class 0.000 claims description 21
- 239000004215 Carbon black (E152) Substances 0.000 claims description 20
- 239000011810 insulating material Substances 0.000 claims description 7
- 238000001816 cooling Methods 0.000 claims description 5
- 239000007789 gas Substances 0.000 description 66
- JKTORXLUQLQJCM-UHFFFAOYSA-N 4-phosphonobutylphosphonic acid Chemical compound OP(O)(=O)CCCCP(O)(O)=O JKTORXLUQLQJCM-UHFFFAOYSA-N 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 7
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 6
- 229910017052 cobalt Inorganic materials 0.000 description 5
- 239000010941 cobalt Substances 0.000 description 5
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 229910000831 Steel Inorganic materials 0.000 description 4
- 239000004071 soot Substances 0.000 description 4
- 239000010959 steel Substances 0.000 description 4
- 238000005979 thermal decomposition reaction Methods 0.000 description 4
- 238000010586 diagram Methods 0.000 description 3
- 238000010791 quenching Methods 0.000 description 3
- 230000000171 quenching effect Effects 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 2
- 238000005255 carburizing Methods 0.000 description 2
- 238000006555 catalytic reaction Methods 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 238000005496 tempering Methods 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000029052 metamorphosis Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000006011 modification reaction Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
- C21D1/74—Methods of treatment in inert gas, controlled atmosphere, vacuum or pulverulent material
- C21D1/76—Adjusting the composition of the atmosphere
- C21D1/763—Adjusting the composition of the atmosphere using a catalyst
-
- 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
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/10—Process efficiency
- Y02P20/129—Energy recovery, e.g. by cogeneration, H2recovery or pressure recovery turbines
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Hydrogen, Water And Hydrids (AREA)
- Solid-Phase Diffusion Into Metallic Material Surfaces (AREA)
Description
〔産業上の利用分野〕
本発明は、吸熱型ガス変成装置に関し、詳しく
は、鋼部品の焼入れ・焼もどし、あるいは、浸炭
焼入等の熱処理時に使用する吸熱型ガスを、低温
活性触媒を用いて850〜950℃の比較的低温で変成
させることのできる吸熱型ガス変成装置にかか
る。
〔従来技術〕
鋼部品の焼入れ・焼もどし、あるいは、浸炭焼
入等の熱処理時に用いる吸熱型ガスは、従来、い
わゆる、RXガス発生炉と呼ばれる、吸熱型ガス
変成装置によつて製造されている。
そして、このRXガス発生炉は、ニツケル触媒
を充填し、850〜1100℃の高温に保持したレトル
ト内へ、メタン(CH4)、エタン(C3H8)、ブタ
ン(C4H10)等の炭化水素ガスと、空気との混合
ガスを送給し、CO,H2,N2を主成分とし、微量
のCH4,H2O,Cを含む、吸熱型ガスを変成さ
せるものである。
ところで、上記従来のRXガス発生炉に用いら
れるニツケル触媒に比して、比較的低温の850〜
950℃で活性なコバルト触媒を使用した場合、従
来のニツケル触媒使用時には、850〜1100℃の高
温でしか反応させることのできなかつた吸熱型ガ
ス変成反応を、850〜950℃の比較的低温にて、上
述のニツケル触媒と同様の吸熱型ガスを変成でき
ることが明らかとなつた。
さて、炭化水素ガスとして、ブタンに例をとつ
て、その変成反応を観察すると、レトルト内で
は、
C4H10+2O2+7.52N2→4CO+5H2+7.52N2な
る反応が進行し、この時、以下の平衡反応が維持
されている。
H2+CO2CO+H2O
CH4+CO22CO+2H2
CH4+H2OCO+3H2
従つて、各成分の間には、CO≒23%,H2≒29
%,CH4=微量〜0.2%,CO2=微量〜2.0%、残
部N2で、互いに平衡状態にある。
そして、ブタンと空気との混合比を変化させる
と、その混合比に応じて、CH4,CO2,H2O等
の平衡値は変化する。
同時に、CO,H2,N2等の平衡値も変化する
が、その割合は少ない。
ところで、この従来の吸熱型ガス変成法におい
ては、炭化水素ガスと空気の混合ガスが、触媒と
接触して変成反応が進行する前に、炭化水素ガス
が熱分解して、すす(C)を生成すると、平衡状態が
くずれて平衡ガスが得られなくなり、CO,CO2
によるカーボンポテンシヤルの制御が困難となる
欠点がある。
さらに、上述のようにして生成されたすす(C)が
触媒に付着して、触媒活性の低下をきたすという
欠点がある。
上述のような、上述技術の欠点を、具体的な従
来装置に基づいて説明すると、第1図において、
ブタン1の0.86l/minと空気2の8.6l/minから
なる混合ガスを、930℃のレトルト6に送給する
と、100c.c.の触媒7のもとで、15l/minの吸熱型
ガス3が変成できるものである。
ここで、従来の変成装置では、レトルト6にお
ける炭化水素ガスの熱分解を防止するため、急速
加熱部6aは、細径パイプ数本からなる多管構造
として、加熱炉からの熱を吸収しやすくし、ガス
の急速加熱を促進するようにしてある。
すなわち、この急速加熱部6aでは、下記のよ
うなブタンの熱分解反応;
C4H10→C↓2CH4+H2
によるすす(C)の生成を抑制するため、空気、ブタ
ンの混合ガスを急速加熱する必要がある。
しかし、従来の吸熱型ガス変成装置のレトルト
6では、上述のように、細径パイプの多管構造と
して、急速加熱を促進すべく考慮されているもの
の、すす(C)の生成を、完全には抑制することがで
きない欠点がある。
〔発明の目的〕
本発明は、鋼部品の熱処理用雰囲気等に用いる
吸熱型ガスを従来のニツケル触媒に比して低温で
活性なコバルト触媒を用いて予め高温に加熱され
た空気に、直接、室温の炭化水素ガスを混合させ
て、炭化水素ガスを伝熱効率よく加熱し、炭化水
素ガスの加熱速度を速めることによつて、炭化水
素ガスの熱分解を確実に抑制でき、しかも、炭化
水素ガスと空気とを混合しやすい構造とすること
によつて触媒反応による平衡状態の吸熱型ガス
を、効率よく変成することができる、吸熱型ガス
変成装置を提供することを目的としている。
〔発明の構成〕
このような目的は、本発明によれば、触媒を充
填し、高温に保持されたレトルト内において、空
気とブタン等の炭化水素ガスとを供給し、混合さ
せて、吸熱型ガスを変成させる吸熱型ガス変成装
置であつて、
前記レトルトはラバール管状に中央部に絞り部
を有する筒形状をなし、加熱炉内に配設されると
ともに、該レトルト内を前記絞り部を境界とし
て、空気余熱室と触媒を充填した触媒充填部にメ
ツシユ状隔膜にて区画し、レトルトの空気余熱室
側端部には、空気供給源からの供給空気量を測
定・制御する流量計を経て、空気予熱室に送給す
る空気供給管が連結され、また、レトルト内触媒
充填室の前記絞り部側には、加熱炉の炉壁部に配
設された冷却構造を有する断熱材を貫通して配設
され、ブタン等の炭化水素ガス供給量を測定・制
御する流量計を経て、炉外配管によつて導かれた
多方向からの複数の、ブタン等の炭化水素ガス供
給管が連結され、さらに、レトルトの触媒充填室
側端部には、変成された変成ガスを冷却するクー
ラーを有する構造としたことを特徴とした吸熱型
ガス変成装置によつて達成される。
〔発明の作用〕
以下、本発明の作用について説明する。
本発明の吸熱型ガス変成装置と従来の吸熱型ガ
ス変成装置の違いは、炭化水素ガスとしてのブタ
ン加熱構造およびその供給構造にある。
従来の吸熱型ガス変成装置では、室温ブタンを
その10倍の容積の室温空気とともに急速加熱する
構造としているため、ブタンの加熱速度が遅くな
るが、本発明の吸熱型ガス変成装置では、予め高
温に加熱されたブタン量の10倍の容積の空気が、
直接、室温のブタンと接触してブタンを加熱する
ため、伝熱効率が非常によく、従つてブタンの加
熱速度が速くなることから、ブタンの熱分解を十
分に抑制でき、平衡状態の吸熱型ガスを変成する
ことができるのである。
さらに、本発明の吸熱型ガス変成装置において
は、ブタンが空気と混合される以前に単独に加熱
されることを防止するため、ブタン供給管と炉の
間に断熱材が配設されており、かつ、その断熱材
は水冷却される構造となつている。
また、本発明の吸熱型ガス変成装置において
は、空気とブタンを均一に混合させる必要がある
ことから、第2図に示すように、空気とブタンの
合流部において、レトルト6の絞り部6dを形成
して、この絞り部6dに多方向からブタンを供給
して、均一な混合ガスとして触媒充填室6bへ送
給する構造としている。
〔実施例〕
以下、添付図面に基づいて、本発明の実施例を
説明する。
第2図に、本発明の吸熱型ガス変成装置の概略
図を示す。
なお、同実施例において、前記第1図の従来例
と、同一または相当部分については、第1図と同
一の符号を付することにより説明を省略する。
また、この実施例では、炭化水素ガスとして、
ブタンに例をとつて説明する。
本発明の吸熱型ガス変成装置の構成は、第2図
から明らかなように、ブタン流量計4、空気流量
計5、空気予熱室6a′と触媒充填室6bが、耐熱
性メツシユ状隔膜6cによつて区画されたレトル
ト6、触媒7、クーラ8、加熱炉9からなつてい
る。
そして、従来の吸熱型ガス変成装置と異なる点
は、ブタン1の供給構造である。
さらに、本発明の吸熱型ガス変成装置のポイン
トとして、空気2とブタン1を均一に混合させる
必要があることから、空気2とブタン1の合流部
において、レトルト6の絞り部6dを形成し、そ
こへ直交する4方向からブタン1を供給し、均一
な混合ガスとして、触媒充填室6bに送給する構
造としている。
このようにして本発明の吸熱型ガス変成装置で
は、空気予熱室6dにおいて、930℃の高温に加
熱した、空気2の8.6l/min中に、炉外配管によ
つて室温に保持された、ブタン1の0.86l/min
を、加熱炉9を貫通して配設された断熱材10に
穿設された直交する4方向の孔から供給し、触媒
充填室6bにおいて、ブタン1を急速に加熱した
後、酸素過剰率を1.05として、空気2と混合させ
て、コバルト触媒7により変成された組成を下表
に示す。
[Industrial Field of Application] The present invention relates to an endothermic gas conversion device, and more specifically, the present invention relates to an endothermic gas conversion device, and more specifically, the endothermic gas used during heat treatment such as quenching and tempering of steel parts or carburizing and quenching is converted into an endothermic gas using a low-temperature active catalyst. This requires an endothermic gas shift device that can perform metamorphosis at a relatively low temperature of 850 to 950°C. [Prior art] Endothermic gas used during heat treatment such as hardening and tempering of steel parts or carburizing and quenching has conventionally been produced by an endothermic gas conversion device called a so-called RX gas generation furnace. . This RX gas generating furnace then supplies methane (CH 4 ), ethane (C 3 H 8 ), butane (C 4 H 10 ), etc. into a retort filled with a nickel catalyst and maintained at a high temperature of 850 to 1100°C. This system supplies a mixed gas of hydrocarbon gas and air, and transforms an endothermic gas containing CO, H 2 , and N 2 as main components, and trace amounts of CH 4 , H 2 O, and C. . By the way, compared to the nickel catalyst used in the conventional RX gas generator mentioned above, the 850~
When using a cobalt catalyst that is active at 950℃, the endothermic gas conversion reaction, which could only be carried out at a high temperature of 850 to 1100℃ when using a conventional nickel catalyst, can be carried out at a relatively low temperature of 850 to 950℃. As a result, it has become clear that endothermic gases similar to those of the above-mentioned nickel catalyst can be modified. Now, if we take butane as an example of a hydrocarbon gas and observe its modification reaction, in the retort the reaction C 4 H 10 + 2O 2 + 7.52N 2 → 4CO + 5H 2 + 7.52N 2 proceeds, and at this time , the following equilibrium reaction is maintained. H 2 +CO 2 CO + H 2 O CH 4 +CO 2 2CO + 2H 2 CH 4 +H 2 OCO + 3H 2 Therefore, between each component, CO≒23%, H 2 ≒29
%, CH 4 = trace amount ~ 0.2%, CO 2 = trace amount ~ 2.0%, and the balance is N 2 , which are in equilibrium with each other. When the mixing ratio of butane and air is changed, the equilibrium values of CH 4 , CO 2 , H 2 O, etc. change depending on the mixing ratio. At the same time, the equilibrium values of CO, H 2 , N 2 etc. also change, but the proportion thereof is small. By the way, in this conventional endothermic gas shift method, before the mixed gas of hydrocarbon gas and air contacts the catalyst and the shift reaction proceeds, the hydrocarbon gas is thermally decomposed to produce soot (C). When generated, the equilibrium state is disrupted and equilibrium gas cannot be obtained, resulting in CO, CO 2
The disadvantage is that it is difficult to control the carbon potential. Furthermore, there is a drawback that the soot (C) produced as described above adheres to the catalyst, resulting in a decrease in catalytic activity. The drawbacks of the above-mentioned technology as described above will be explained based on a specific conventional device. In FIG.
When a mixed gas consisting of 0.86 l/min of butane 1 and 8.6 l/min of air 2 is fed to the retort 6 at 930°C, 15 l/min of endothermic gas flows under the catalyst 7 of 100 c.c. 3 can be transmuted. Here, in the conventional shift converter, in order to prevent thermal decomposition of the hydrocarbon gas in the retort 6, the rapid heating section 6a has a multi-tubular structure consisting of several small diameter pipes, which easily absorbs heat from the heating furnace. This is designed to promote rapid heating of the gas. That is, in this rapid heating section 6a, a mixed gas of air and butane is rapidly heated in order to suppress the generation of soot (C) due to the following thermal decomposition reaction of butane: C 4 H 10 →C↓2CH 4 + H 2 Needs to be heated. However, as mentioned above, the retort 6 of the conventional endothermic gas shift converter has a multi-tube structure of small diameter pipes, which is designed to promote rapid heating, but it does not completely prevent the generation of soot (C). has drawbacks that cannot be suppressed. [Object of the Invention] The present invention is directed to the use of an endothermic gas used in an atmosphere for heat treatment of steel parts, etc., to air that has been preheated to a high temperature using a cobalt catalyst that is active at a lower temperature than a conventional nickel catalyst. By mixing hydrocarbon gases at room temperature, heating the hydrocarbon gases with high heat transfer efficiency, and increasing the heating rate of the hydrocarbon gases, thermal decomposition of the hydrocarbon gases can be reliably suppressed. An object of the present invention is to provide an endothermic gas shift device that can efficiently transform endothermic gas in an equilibrium state through a catalytic reaction by having a structure that allows easy mixing of gas and air. [Structure of the Invention] According to the present invention, air and a hydrocarbon gas such as butane are supplied and mixed in a retort filled with a catalyst and maintained at a high temperature to produce an endothermic type gas. The retort is a cylindrical Laval tubular shape having a constricted part in the center, and is arranged in a heating furnace, and the retort is arranged inside the retort with the constricted part as a boundary. The retort is divided into an air preheating chamber and a catalyst filling section filled with catalyst with a mesh-like diaphragm, and a flow meter is installed at the end of the air preheating chamber side of the retort to measure and control the amount of air supplied from the air supply source. , an air supply pipe for feeding into the air preheating chamber is connected, and a heat insulating material having a cooling structure disposed on the furnace wall of the heating furnace is connected to the constriction section side of the in-retort catalyst filling chamber. A plurality of butane and other hydrocarbon gas supply pipes are connected from multiple directions by external piping through a flowmeter that measures and controls the amount of butane and other hydrocarbon gas supplied. Furthermore, this is achieved by an endothermic gas shift apparatus characterized in that the end of the retort on the side of the catalyst filling chamber has a cooler for cooling the shifted gas. [Action of the invention] The action of the present invention will be explained below. The difference between the endothermic gas shift device of the present invention and the conventional endothermic gas shift device lies in the structure for heating butane as a hydrocarbon gas and the structure for supplying it. Conventional endothermic gas shift equipment has a structure in which room temperature butane is rapidly heated together with room temperature air 10 times its volume, which slows down the heating rate of butane. A volume of air 10 times the amount of butane heated to
Since the butane is heated by direct contact with butane at room temperature, the heat transfer efficiency is very high, and the heating rate of butane is therefore fast, so the thermal decomposition of butane can be sufficiently suppressed and it becomes an endothermic gas in an equilibrium state. can be transformed. Furthermore, in the endothermic gas shift apparatus of the present invention, in order to prevent butane from being heated independently before being mixed with air, a heat insulating material is provided between the butane supply pipe and the furnace. Moreover, the heat insulating material is water-cooled. In addition, in the endothermic gas conversion apparatus of the present invention, since it is necessary to mix air and butane uniformly, as shown in FIG. The structure is such that butane is supplied from multiple directions to this constricted portion 6d and is delivered as a uniform mixed gas to the catalyst filling chamber 6b. [Example] Hereinafter, an example of the present invention will be described based on the accompanying drawings. FIG. 2 shows a schematic diagram of the endothermic gas shift apparatus of the present invention. In this embodiment, the same or corresponding parts as those in the conventional example shown in FIG. 1 are given the same reference numerals as in FIG. 1, and the explanation thereof will be omitted. In addition, in this example, as a hydrocarbon gas,
This will be explained using butane as an example. As is clear from FIG. 2, the configuration of the endothermic gas shift apparatus of the present invention is such that a butane flow meter 4, an air flow meter 5, an air preheating chamber 6a', and a catalyst filling chamber 6b are connected to a heat-resistant mesh-like diaphragm 6c. It consists of a retort 6, a catalyst 7, a cooler 8, and a heating furnace 9, which are divided into sections. The difference from the conventional endothermic gas shift apparatus is the butane 1 supply structure. Furthermore, as a point of the endothermic gas shift apparatus of the present invention, it is necessary to uniformly mix the air 2 and the butane 1, so the constricted part 6d of the retort 6 is formed at the confluence of the air 2 and the butane 1, Butane 1 is supplied from four directions perpendicular thereto, and the structure is such that it is delivered as a uniform mixed gas to the catalyst filling chamber 6b. In this manner, in the endothermic gas shift apparatus of the present invention, air 2 is heated to a high temperature of 930° C. at 8.6 l/min in the air preheating chamber 6d, and is maintained at room temperature by the piping outside the furnace. 0.86l/min of butane 1
is supplied from holes in four orthogonal directions drilled in a heat insulating material 10 that penetrates the heating furnace 9, and after rapidly heating the butane 1 in the catalyst filling chamber 6b, the oxygen excess rate is reduced. 1.05, the composition of which was mixed with air 2 and modified by cobalt catalyst 7 is shown in the table below.
以上により明らかなように、本発明にかかる吸
熱型ガス変成装置によれば、鋼部品の熱処理用雰
囲気等に用いる吸熱型ガスを従来のニツケル触媒
に比して低温で活性なコバルト触媒を用いて予め
高温に加熱された空気に、直接、室温の炭化水素
ガスを混合させて、炭化水素ガスを伝熱効率よく
加熱し、炭化水素ガスの昇温速度を速めることに
よつて、炭化水素ガスの熱分解を確実に抑制で
き、しかも、炭化水素ガスと空気とを混合しやす
い構造とすることによつて触媒反応による平衡状
態の吸熱型ガスを、効率よく変成することができ
る利点がある。
As is clear from the above, according to the endothermic gas shift apparatus according to the present invention, the endothermic gas used in the atmosphere for heat treatment of steel parts, etc. is made using a cobalt catalyst that is active at a lower temperature than the conventional nickel catalyst. By directly mixing hydrocarbon gas at room temperature with air that has been preheated to a high temperature, the hydrocarbon gas is heated with good heat transfer efficiency, and the heating rate of the hydrocarbon gas is accelerated. By having a structure in which decomposition can be reliably suppressed and hydrocarbon gas and air are easily mixed, there is an advantage that an endothermic gas in an equilibrium state due to a catalytic reaction can be efficiently transformed.
第1図は、従来の吸熱型ガス変成装置の概略
図、第2図は、本発明の吸熱型ガス変成装置の概
略図である。
1……ブタン、2……空気、3……吸熱型ガ
ス、4……ブタン流量計、5……空気流量計、6
……レトルト、6a……急速加熱部、6a′……空
気予熱室、6b……触媒充填室、6c……メツシ
ユ状隔膜、6d……絞り部、7……コバルト触
媒、8……クーラ、9……加熱炉、10……断熱
材、11……冷却水配管。
FIG. 1 is a schematic diagram of a conventional endothermic gas shift device, and FIG. 2 is a schematic diagram of an endothermic gas shift device of the present invention. 1... Butane, 2... Air, 3... Endothermic gas, 4... Butane flow meter, 5... Air flow meter, 6
... Retort, 6a ... Rapid heating section, 6a' ... Air preheating chamber, 6b ... Catalyst filling chamber, 6c ... Meshed diaphragm, 6d ... Throttle section, 7 ... Cobalt catalyst, 8 ... Cooler, 9...Heating furnace, 10...Insulating material, 11...Cooling water piping.
Claims (1)
において、空気とブタン等の炭化水素ガスとを供
給し、混合させて、吸熱型ガスを変成させる吸熱
型ガス変成装置であつて、 前記レトルトはラバール管状に中央部に絞り部
を有する筒形状をなし、加熱炉内に配設されると
ともに、該レトルト内を前記絞り部を境界とし
て、空気余熱室と触媒を充填した触媒充填部にメ
ツシユ状隔膜にて区画し、レトルトの空気余熱室
側端部には、空気供給源からの供給空気量を測
定・制御する流量計を経て、空気予熱室に送給す
る空気供給管が連結され、また、レトルト内触媒
充填室の前記絞り部側には、加熱炉の炉壁部に配
設された冷却構造を有する断熱材を貫通して配設
され、ブタン等の炭化水素ガス供給量を測定・制
御する流量計を経て、炉外配管によつて導かれた
多方向からの複数の、ブタン等の炭化水素ガス供
給管が連結され、さらに、レトルトの触媒充填室
側端部には、変成された変成ガスを冷却するクー
ラーを有する構造としたことを特徴とした吸熱型
ガス変成装置。[Claims] 1. An endothermic gas shift device that supplies and mixes air and hydrocarbon gas such as butane in a retort filled with a catalyst and maintained at a high temperature to convert endothermic gas. The retort has a cylindrical shape in the form of a Laval tube with a constriction in the center, and is disposed in a heating furnace, and the retort is filled with an air preheating chamber and a catalyst, with the constriction as a boundary. The catalyst filling part is divided by a mesh-like diaphragm, and the end of the retort on the air preheating chamber side is supplied with air that is sent to the air preheating chamber via a flow meter that measures and controls the amount of air supplied from the air supply source. A pipe is connected to the constriction part side of the catalyst filling chamber in the retort, and a heat insulating material having a cooling structure provided on the wall of the heating furnace is disposed so as to pass through a heat insulating material having a cooling structure to absorb hydrocarbons such as butane. A plurality of butane and other hydrocarbon gas supply pipes are connected from multiple directions led by external piping through a flow meter that measures and controls the gas supply amount. An endothermic gas shift device characterized by having a structure including a cooler for cooling the metamorphosed gas.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59003228A JPS60149713A (en) | 1984-01-10 | 1984-01-10 | Endothermic type gas converter |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59003228A JPS60149713A (en) | 1984-01-10 | 1984-01-10 | Endothermic type gas converter |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60149713A JPS60149713A (en) | 1985-08-07 |
| JPH0418009B2 true JPH0418009B2 (en) | 1992-03-26 |
Family
ID=11551588
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59003228A Granted JPS60149713A (en) | 1984-01-10 | 1984-01-10 | Endothermic type gas converter |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60149713A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010024535A (en) * | 2008-07-24 | 2010-02-04 | Aisin Seiki Co Ltd | Carburization method for steel |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2009299163A (en) * | 2008-06-16 | 2009-12-24 | Ntn Corp | Heat-treatment method for steel, method for manufacturing machine parts, and machine parts |
-
1984
- 1984-01-10 JP JP59003228A patent/JPS60149713A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010024535A (en) * | 2008-07-24 | 2010-02-04 | Aisin Seiki Co Ltd | Carburization method for steel |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS60149713A (en) | 1985-08-07 |
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