JPS6081002A - Endothermic gas conversion process and its apparatus - Google Patents
Endothermic gas conversion process and its apparatusInfo
- Publication number
- JPS6081002A JPS6081002A JP58190424A JP19042483A JPS6081002A JP S6081002 A JPS6081002 A JP S6081002A JP 58190424 A JP58190424 A JP 58190424A JP 19042483 A JP19042483 A JP 19042483A JP S6081002 A JPS6081002 A JP S6081002A
- Authority
- JP
- Japan
- Prior art keywords
- gas
- air
- retort
- butane
- 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.)
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Classifications
-
- 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
-
- 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
- Hydrogen, Water And Hydrids (AREA)
Abstract
Description
【発明の詳細な説明】
イ、産業上の利用分野
本発明は、吸熱型ガス変成方法およびその装置に関し、
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、触媒を用い
て850〜1100 ’cの高温で変成させる、吸熱型
ガス変成方法およびその装置にかかる。DETAILED DESCRIPTION OF THE INVENTION A. Field of Industrial Application The present invention relates to an endothermic gas conversion method and an apparatus thereof;
In detail, an endothermic gas transformation method and apparatus that uses a catalyst to transform endothermic gas used during heat treatment such as quenching and tempering of steel parts or carburizing and quenching at a high temperature of 850 to 1100'C. It takes.
口、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って製造
されている。BACKGROUND ART Endothermic gas used during heat treatment such as hardening and tempering of steel parts or carburizing and quenching is conventionally produced by an endothermic gas conversion device called a so-called RX gas generating furnace.
そして、このRXガス発生炉は、ニッケル触媒を充填し
、850〜1100℃の高温に保持したレトルト内へ、
メタン(CH4)プロパン(c。This RX gas generator is then filled with a nickel catalyst and placed into a retort maintained at a high temperature of 850 to 1100°C.
Methane (CH4) Propane (c.
H8)、ブタン(C4H,、)等の炭化水素ガスと、空
気との混合ガスを送給し、C01H2、N2を主成分と
し、微量のCH4、■1□o、、cを含む、吸熱型ガス
を変成させるものである。Endothermic type that supplies a mixed gas of hydrocarbon gas such as H8), butane (C4H,, ), and air, and contains C01H2, N2 as the main components, and trace amounts of CH4, ■1□o,, c. It metamorphoses gas.
さて、炭化水素ガスとして、ブタンに例をとって、その
変成反応を観察すると、レトルト内では、C4H16+
202 +7.52N l→4 CO+ 5 H+ 7
.52N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。Now, if we take butane as an example of a hydrocarbon gas and observe its modification reaction, in the retort, C4H16+
202 +7.52N l→4 CO+ 5 H+ 7
.. 52N reaction progresses, and at this time the following equilibrium reaction is maintained.
H2+CO2:CO+H20
CHa + COrw−−2CO+2 H2CH,+H
20≠CO+3H2
従って、各成分の間には、CO#23%、H2#29%
、CH,= 微量〜0.2%、CO,−微量〜2.0%
、残部N2で、互いに平衡状態にある。H2+CO2:CO+H20 CHa + COrw--2CO+2 H2CH,+H
20≠CO+3H2 Therefore, between each component, CO#23%, H2#29%
, CH, = trace ~ 0.2%, CO, - trace ~ 2.0%
, and the remainder N2 are in equilibrium with each other.
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、H20等の平衡値は
変化する。Then, when the mixing ratio of butane and air is changed, the equilibrium values of CH4, co2, H20, etc. change depending on the mixing ratio.
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、C01C02によるカーボンボテ5ンシヤ
ルの制御が困難となる欠点がある。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 and soot (
If C) is produced, the equilibrium state will be disrupted, making it impossible to obtain an equilibrium gas, and there is a drawback that it will be difficult to control the carbon dynamics by C01C02.
さらに、上述のようにして生成されたすす(C)が触媒
にイ」着して、触媒活性の低下をきたすという欠点があ
る。Furthermore, there is a drawback that the soot (C) produced as described above adheres to the catalyst, resulting in a decrease in catalyst activity.
上述のような、従来技術の欠点を、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.
86j! / minと空気2の8.61 / min
からなる混合ガスを、930℃のレトルト6に送給する
と、100ccの触媒7のもとで、151/minの吸
熱型ガス3が変成できるものである。The above-mentioned drawbacks of the prior art will be explained based on a specific conventional device. In FIG.
86j! / min and air 2 8.61 / min
When a mixed gas composed of
ここで、従来の変成方法では、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
しである
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;
C4H1,、→C↓+2 CHa + 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。Here, in the conventional shift conversion method, in order to prevent thermal decomposition of hydrocarbon gas in the retort 6, the rapid heating section 6a is
It has a multi-tube structure consisting of several small diameter pipes to easily absorb heat from the heating furnace and promote rapid heating of the gas. Decomposition reaction: C4H1,,→C↓+2 CHa + In order to suppress the production of soot (C) by H2, it is necessary to rapidly heat the mixed gas of air and butane.
しかし、従来の吸熱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、すず(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。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 cannot completely prevent the formation of tin (C). There are drawbacks that cannot be suppressed.
ハ0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、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って、
炭化水素ガスの熱分解を確実に抑制でき、しかも、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、吸熱型ガス変成方法およびその装置を提
供することを目的としている。C0 Purpose of the Invention The present invention aims to improve heat transfer efficiency by directly mixing room temperature hydrocarbon gas with air that has been preheated to a high temperature using an endothermic gas used in an atmosphere for heat treatment of steel parts. By heating well and increasing the heating rate of the hydrocarbon gas,
It is an object of the present invention to provide an endothermic gas conversion method and apparatus that can reliably suppress thermal decomposition of hydrocarbon gas and efficiently convert endothermic gas in an equilibrium state through a catalytic reaction.
二1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、ブタン等の炭化水素ガス
と空気との混合ガスを供給して、吸熱型ガスを変成させ
る、吸熱型ガス変成力法およびその装置であって、
上記レトルトを、予熱室と触媒充填室にメソシュ状隔膜
により区画して、空気は、予熱室にて予熱された後、触
媒充填室に送給され、一方、ブタン等の炭化水素ガスは
、炭化水素ガスの熱分解を防止するとともに、変成反応
により平衡ガスを効率的に得られるように、炉外配管に
より、予熱することなく、直接、触媒充填室に送給する
ことにより、予熱された空気によって、炭化水素ガスを
急速に加熱・混合し、触媒と接触させて吸熱型ガスを変
成することを特徴とした吸熱型ガス変成方法、および、
上記レトルトは、加熱炉内に配設されるとともに、該レ
トルト内を空気予熱室と触媒を充填した触媒充填室に、
メソシュ状隔膜にて区画し、レトルトの空気予熱室側端
部には、空気供給源からの空気供給量を測定・制御する
流量計を経て、空気を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には、加熱炉
の炉壁部に配設された断熱材を貫通して配管され、ブタ
ン等の炭化水素ガス供給量を測定・制御する流量針を経
て、炉外配管によって導かれた、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λ側
端部には、変成された変成ガスを冷却するクーラーが連
結された構造とすることにより、予熱された空気によっ
て、炭化水素ガスを急速に加熱・混合させ、効率的に吸
熱型ガスを変成することのできることを特徴とした、吸
熱型ガス変成装置によって達成される。21 Structure of the Invention According to the present invention, a mixed gas of a hydrocarbon gas such as butane and air is supplied into a retort filled with a catalyst and maintained at a high temperature to produce an endothermic type gas. An endothermic gas transformation force method and apparatus for transforming gas, wherein the retort is divided into a preheating chamber and a catalyst filling chamber by a mesoche-like diaphragm, and the air is preheated in the preheating chamber and then charged with the catalyst. On the other hand, hydrocarbon gas such as butane must be preheated by piping outside the furnace to prevent thermal decomposition of the hydrocarbon gas and to efficiently obtain equilibrium gas through a shift reaction. This is an endothermic gas characterized by the fact that the hydrocarbon gas is rapidly heated and mixed with preheated air by directly feeding it into the catalyst-filled chamber, and then brought into contact with the catalyst to convert the endothermic gas into an endothermic gas. Metamorphosis method, and
The retort is arranged in a heating furnace, and the retort has an air preheating chamber and a catalyst filling chamber filled with a catalyst.
It is divided by a mesoche-like diaphragm, and at the end of the retort on the air preheating chamber side, there is an air supply pipe that supplies air to the air preheating chamber via a flow meter that measures and controls the amount of air supplied from the air supply source. The gas is connected to the catalyst filling chamber in the retort, and is piped through the heat insulating material installed on the furnace wall of the heating furnace, through a flow rate needle that measures and controls the amount of hydrocarbon gas such as butane supplied. A hydrocarbon gas supply pipe such as butane, which is guided by an external piping, is connected to the retort, and a cooler is connected to the end of the retort on the catalyst-filled λ side to cool the transformed gas. This is achieved by an endothermic gas shift device that is characterized by being able to rapidly heat and mix hydrocarbon gas using preheated air and efficiently transform endothermic gas.
ホ、実施例 以下、添付図面に基づいて、本発明の詳細な説明する。E, Example Hereinafter, the present invention will be described in detail based on the accompanying drawings.
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−
又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。FIG. 2 shows a schematic diagram of the endothermic gas shift apparatus of the present invention. In the same embodiment, the conventional example shown in FIG.
Or equivalent parts will be designated by the same reference numerals as in FIG. 1, and their explanation will be omitted.
また、この実施例では、炭化水素ガスとして、ブタンに
例をとって説明する。Further, in this example, explanation will be given using butane as an example of the hydrocarbon gas.
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、メソシュ状隔膜6cによ
って区画されたレトルト6、触媒7、クーラ8、加熱炉
9がらなっている。As is clear from FIG. 2, the configuration of the endothermic gas conversion 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 partitioned by a mesh-shaped diaphragm 6c. It consists of a retort 6, a catalyst 7, a cooler 8, and a heating furnace 9.
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の供給方法である。The difference from conventional endothermic gas shift equipment is the method of supplying butane 1.
本発明の吸熱型ガス変成装置では、空気予熱室6a’に
おいて、930°Cの高温に加熱した、空気2の8.6
ρ/min中に、炉外配管によって室温に保持された、
ブタン1の0.86ff / minを、加Q炉9を貫
通して配設された断熱材10に穿設された孔から供給し
、触媒充填室6bにおいて、ブタンlを急速に加熱した
後、酸素過剰率を1.05として、空気と混合させて、
触媒により変成された組成を下表に示す。In the endothermic gas shift apparatus of the present invention, 8.6% of the air 2 is heated to a high temperature of 930°C in the air preheating chamber 6a'.
maintained at room temperature by external piping during ρ/min,
After supplying 0.86 ff/min of butane 1 from a hole drilled in a heat insulating material 10 that penetrates the heating furnace 9 and rapidly heating the butane 1 in the catalyst filling chamber 6b, Mix with air at an oxygen excess rate of 1.05,
The composition modified by the catalyst is shown in the table below.
表から明らかなように、従来の吸熱型ガス変成装置で変
成された吸熱型ガス組成は、COlおよびH2が平衡吸
熱ガス組成に比べ、低目の値であり、しかも、変成反応
に伴ない、すず(C)の生成が認められるのに対し、本
発明の吸熱型ガス変成装置によって変成された吸熱型ガ
ス組成は、はぼ、平衡吸熱型ガス組成に近似しており、
しがも、変成反応に伴なう、すす(C)の生成は認めら
れない。As is clear from the table, the endothermic gas composition metamorphosed by the conventional endothermic gas shift device has lower values of COl and H2 than the equilibrium endothermic gas composition, and, moreover, as a result of the metamorphosis reaction, While the formation of tin (C) is observed, the endothermic gas composition transformed by the endothermic gas shift device of the present invention is very close to the equilibrium endothermic gas composition,
However, the production of soot (C) accompanying the metamorphosis reaction was not observed.
へ0発明の作用効果
以上により明らかなように、本発明にががる吸熱型ガス
変成方法およびその装置によれば、鋼部品の熱処理用雰
囲気等に用いる吸熱型ガスを、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!!)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って、炭化水素ガスの熱分解を確
実に抑制でき、しかも、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。Effects of the Invention As is clear from the above, according to the endothermic gas transformation method and apparatus of the present invention, the endothermic gas used in the atmosphere for heat treatment of steel parts is heated to a high temperature in advance. Directly mix hydrocarbon gas at room temperature with air to transmit hydrocarbon gas! ! ) By heating efficiently and accelerating the heating rate of hydrocarbon gas, thermal decomposition of hydrocarbon gas can be reliably suppressed, and endothermic gas in an equilibrium state due to catalytic reaction can be efficiently transformed. There is.
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。
1−一−−ブタン
2−−−−−一空気
3−−−一吸熱型ガス
4−−−−ブタン流量計
5−−一一−−空気流量計
6−−−−レトルト
6 a−−−−急速加熱部
6 a ’ −−一空気予熱室
6b−−−−一触媒充填室
7−−−−触媒
8−−−−−クーラ
9−−−−一加熱炉
10−・−・−断熱材
出願人 トヨタ自動車4おし釦仕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. 1-1--Butane 2-----1 Air 3--1 Endothermic gas 4--Butane flow meter 5--11--Air flow meter 6-----Retort 6 a-- --- Rapid heating section 6 a' --- Air preheating chamber 6 b --- Catalyst filling chamber 7 --- Catalyst 8 --- Cooler 9 ---- Heating furnace 10 --- Insulation material applicant: Toyota Motor Corporation
Claims (1)
タン等の炭化水素ガスと空気との混合ガスを供給して、
吸熱型ガスを変成させる、吸熱型ガス変成方法であって
、 上記レトルトを、予熱室と触媒充填室にメソシュ状隔膜
により区画して、空気は、予熱室にて予熱された後、触
媒充填室に送給され、一方、ブタン等の炭化水素ガスは
、炭化水素ガスの熱分解を防止するとともに、変成反応
により平衡ガスを効率的に得られるように、炉外配管に
より、予熱することなく、直接、触媒充填室に送給する
ことにより、予熱された空気によって、炭化水素ガスを
急速に加熱・混合し、触媒と接触させて吸熱型ガスを変
成することを特徴とした吸熱型ガス変成方法。 2、触媒を充填し、高温に保持されたレトルト内に、ブ
タン等の炭化水素ガスと空気との混合ガスを供給して、
吸熱型ガスを変成させる、吸熱型ガス変成装置であって
、 上記レトルトは、加熱炉内に配設されるとともに、該レ
トルト内を空気予熱室と触媒を充填した触媒充填室に、
メソシュ状隔膜にて区画し、レトルトの空気予熱室側端
部には、空気供給源からの空気供給量を測定・制御する
流量計を経て、空気を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には、加熱炉
の炉壁部に配設された断熱材を貫通して配管され\ブタ
ン等の炭化水素ガス供給量を測定・制御する流量針を経
て、炉外配管によって導かれた、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が連
結された構造とすることにより、予熱された空気によっ
て、炭化水素ガスを急速に加熱・混合させ、効率的に吸
熱型ガスを変成することのできることを特徴とした、吸
熱型ガス変成装置。[Claims] (1) Supplying a mixed gas of a hydrocarbon gas such as butane and air into a retort filled with a catalyst and maintained at a high temperature,
An endothermic gas transformation method for transforming an endothermic gas, wherein the retort is divided into a preheating chamber and a catalyst filling chamber by a mesoche-like diaphragm, and the air is preheated in the preheating chamber and then transferred to the catalyst filling chamber. On the other hand, hydrocarbon gas such as butane is supplied to the reactor via external piping without preheating, in order to prevent thermal decomposition of the hydrocarbon gas and to efficiently obtain equilibrium gas through a shift reaction. An endothermic gas transformation method characterized by rapidly heating and mixing hydrocarbon gas with preheated air by directly feeding it into a catalyst filling chamber, and bringing it into contact with a catalyst to transform endothermic gas. . 2. Supplying a mixed gas of a hydrocarbon gas such as butane and air into a retort filled with a catalyst and maintained at a high temperature,
An endothermic gas shift device that transforms an endothermic gas, the retort being disposed in a heating furnace, the retort being connected to an air preheating chamber and a catalyst filling chamber filled with a catalyst.
It is divided by a mesoche-like diaphragm, and at the end of the retort on the air preheating chamber side, there is an air supply pipe that supplies air to the air preheating chamber via a flow meter that measures and controls the amount of air supplied from the air supply source. In addition, the catalyst filling chamber in the retort is piped through a heat insulating material installed on the furnace wall of the heating furnace, and is connected to the catalyst filling chamber through a flow rate needle that measures and controls the amount of hydrocarbon gas such as butane supplied. A hydrocarbon gas supply pipe such as butane, which is led by an external piping, is connected to the retort, and a cooler is connected to the end of the retort on the catalyst filling chamber side to cool the transformed gas. An endothermic gas shift device characterized by being able to rapidly heat and mix hydrocarbon gas with preheated air and efficiently transform endothermic gas.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58190424A JPS6081002A (en) | 1983-10-12 | 1983-10-12 | Endothermic gas conversion process and its apparatus |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58190424A JPS6081002A (en) | 1983-10-12 | 1983-10-12 | Endothermic gas conversion process and its apparatus |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6081002A true JPS6081002A (en) | 1985-05-09 |
| JPH0453804B2 JPH0453804B2 (en) | 1992-08-27 |
Family
ID=16257900
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58190424A Granted JPS6081002A (en) | 1983-10-12 | 1983-10-12 | Endothermic gas conversion process and its apparatus |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6081002A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2012134885A3 (en) * | 2011-03-25 | 2012-12-27 | The United States Of America, As Represented By The Secretary Of Agriculture | Fast pyrolysis catalytic cracking pipe for producing bio-oils |
-
1983
- 1983-10-12 JP JP58190424A patent/JPS6081002A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2012134885A3 (en) * | 2011-03-25 | 2012-12-27 | The United States Of America, As Represented By The Secretary Of Agriculture | Fast pyrolysis catalytic cracking pipe for producing bio-oils |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0453804B2 (en) | 1992-08-27 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |