JPS6110003A - Device for modifying fuel - Google Patents

Device for modifying fuel

Info

Publication number
JPS6110003A
JPS6110003A JP12736384A JP12736384A JPS6110003A JP S6110003 A JPS6110003 A JP S6110003A JP 12736384 A JP12736384 A JP 12736384A JP 12736384 A JP12736384 A JP 12736384A JP S6110003 A JPS6110003 A JP S6110003A
Authority
JP
Japan
Prior art keywords
temperature
fuel
modifying
fed
piping
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
Application number
JP12736384A
Other languages
Japanese (ja)
Inventor
Motohei Katsuta
勝田 基平
Kenichi Hisamatsu
健一 久松
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mitsubishi Heavy Industries Ltd
Original Assignee
Mitsubishi Heavy Industries Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Mitsubishi Heavy Industries Ltd filed Critical Mitsubishi Heavy Industries Ltd
Priority to JP12736384A priority Critical patent/JPS6110003A/en
Publication of JPS6110003A publication Critical patent/JPS6110003A/en
Pending legal-status Critical Current

Links

Landscapes

  • Hydrogen, Water And Hydrids (AREA)

Abstract

PURPOSE:To modify fuel economically by simplifying a process without modifying a low-temperature CO modifying device, by feeding a desorbed gas of a CO desorption column set at the outlet of a high-temperature CO modifying device of a device for modifying fuel to the inlet of the modifying device. CONSTITUTION:A hydrocarbon raw material is fed through the pipings 6 and 7 to the desulfurizer 3 to remove S, it and steam fed from the piping 9 are sent to the fuel modifing catalyst tube 2 set in the furnace 1, heated, processed into CO and H2, fed through the pipings 10 and 11 to the high-temperature CO modifying device 4, converted into CO2 and H2, sent through the pipings 12 and 14 to the CO adsorption column 5, the unreacted CO is adsorbed and removed, and fed through the piping 15 to the following device. On the other hand, steam, etc. is sent from the piping 16 to the other adsorption column 5', desorbed CO is fed through 17 to the high-temperature modifying device 4. Consequently, remaining CO can be reduced without laying a low-temperature CO modifying device, and the fuel is modified efficiently and econimically.

Description

【発明の詳細な説明】 本発明は、燃料改質装fRK関する。[Detailed description of the invention] The present invention relates to a fuel reformer fRK.

従来の技術 炭化水素に水蒸気を加え工水素へ改質する燃料改質装置
においては、従来、高温及び低温CO変成装置と夫々の
前後に熱交換器を設けた系で成り立っていた。この為に
、残留CO 1lIHiを下げる為には、高温・低温C
O変成装置の性能を高める必要があり、その性能が高め
られなければ後段で使われる、例えば、燃料電池の寿命
な低下する欠点があった。
Conventional Technology A fuel reformer that adds steam to hydrocarbons to reform them into technical hydrogen has conventionally consisted of a system including high-temperature and low-temperature CO shift devices and heat exchangers installed before and after each. For this reason, in order to lower the residual CO 1lIHi, high and low temperature C
It is necessary to improve the performance of the O-transformer, and if the performance is not improved, the lifespan of fuel cells used in subsequent stages, for example, will be shortened.

発明が解決しようとする問題点 本発明の目的は、燃料改質装置後段への残存CO量を少
(するとともに、CO変成装置の性能を落としてプラン
トコストを下げることにある。上記本発明の目的は、最
近の秀れたCO吸着剤の開発によって実現されたもので
ある。
Problems to be Solved by the Invention An object of the present invention is to reduce the amount of CO remaining in the latter stage of the fuel reformer (and reduce the plant cost by lowering the performance of the CO shift converter. This objective has been realized due to the recent development of excellent CO adsorbents.

問題点を解決するための手段 本発明は、炭化水素に水蒸気を加えて水素へ改質する装
置において、高温CO変成装置の出口1ccO吸着塔を
設け、該CO吸着塔の脱ガス工程では、脱ガスを該CO
変成装置の入口側に供給する手段を備えたことを特徴と
する燃料改質装置に関する。
Means for Solving the Problems The present invention provides an apparatus for reforming hydrocarbons into hydrogen by adding steam to them, in which a 1 cc O adsorption tower is provided at the outlet of a high-temperature CO shift apparatus, and in the degassing process of the CO adsorption tower, the degassing gas to the CO
The present invention relates to a fuel reformer characterized in that it is equipped with means for supplying the fuel to the inlet side of the shift converter.

以下に、本発明の構成を図面に基づき説明する0 第1図に、本発明の詳細な説明する燃料改質装置のフロ
ーの一部を示す。図中、1は加熱炉、2は水蒸気改質反
応を行なわしめる燃料改質触媒管、6は触媒の保穫の為
に設けられた脱硫装置、4は改質反応後に生成する一酸
化炭素(CO)を炭酸ガス(COりと水素(f(りK転
化する装置で、高温CO変成装置である。5及び5′は
CO吸着塔である。
The configuration of the present invention will be explained below based on the drawings. Fig. 1 shows a part of the flow of a fuel reformer to explain the present invention in detail. In the figure, 1 is a heating furnace, 2 is a fuel reforming catalyst tube that performs a steam reforming reaction, 6 is a desulfurization device installed to preserve the catalyst, and 4 is carbon monoxide (carbon monoxide) produced after the reforming reaction. This is a high-temperature CO conversion device that converts CO) into carbon dioxide gas (CO) and hydrogen (f). 5 and 5' are CO adsorption towers.

作用 炭化水素系原料は配管6より供給され、配管7を軽て脱
硫装置6に供給され、ここでイオウが除去され、配管9
により供給される水蒸気とともに配管8にて燃料改質触
媒管2に供給される。そして、加熱炉IK”C加熱され
℃、炭化水素がCOとH2に改質され、配管10.11
を経て高温CO変成装置4に導入される。こへで、CO
はさらにCO、とH3に変えられ、配管12゜14によ
りCO吸着塔5に導入される。ここで、未反応COが除
去され、配管15にて次段の設備へ供給される。この間
K、他の一つのCO吸着塔5’には配管16より、例え
ば、CO変成後の熱ガスの一部或いは水蒸気が供給され
、脱着したCOが配管17で再び高温のCO変成装置4
へ供給される。CO吸着塔5,5′の吸脱着には、CO
変成装置4のあとのガスがもっている熱エネルギーを吸
収冷凍機で冷源として吸着して、或は直接加熱して脱着
く有効に使うことができる。また、配管13は、一部ガ
スを循環しCw、料の脱硫を行なうものである。
The working hydrocarbon raw material is supplied through a pipe 6, and is supplied through a pipe 7 to a light desulfurization device 6, where sulfur is removed, and then to a pipe 9.
The fuel is supplied to the fuel reforming catalyst tube 2 through the pipe 8 along with the water vapor supplied by the fuel. Then, the heating furnace IK"C is heated to reform the hydrocarbons into CO and H2, and the pipe 10.11
It is then introduced into the high temperature CO converter 4. Here, CO
is further converted into CO, and H3, which are introduced into the CO adsorption tower 5 via piping 12.14. Here, unreacted CO is removed and supplied to the next stage equipment via piping 15. During this time, for example, a part of the hot gas after CO transformation or water vapor is supplied to the other CO adsorption tower 5' from the piping 16, and the desorbed CO is returned to the high temperature CO transformation device 4 through the piping 17.
supplied to For adsorption and desorption in the CO adsorption towers 5 and 5', CO
The thermal energy possessed by the gas after the shift converter 4 can be effectively used by adsorbing it as a cold source with an absorption refrigerator or by directly heating it and desorbing it. Further, the piping 13 is used to partially circulate gas and desulfurize the Cw material.

上記例では温度変動方式での吸収剤での例を示している
。例えば、塩化第一銅系の溶液(C05ORB  溶剤
として知られるもの)を使った吸収剤では、常温近くで
COを吸収し、120℃で放出再生することができる。
The above example shows an example using an absorbent using a temperature fluctuation method. For example, an absorbent using a cuprous chloride-based solution (known as a C05ORB solvent) can absorb CO at near room temperature and release and regenerate it at 120°C.

圧力変動方式で性能の良い吸着剤もある。例えば、鉄・
銅尋の金属をドープしたゼオライト系吸着剤は、数に9
 /as”で吸着し、減圧することにより脱着が可能で
ある。この場合には、加圧用コンプレツサと減圧脱着用
真空ポンプが必要である。
There are also adsorbents that use a pressure fluctuation method and have good performance. For example, iron
The zeolite adsorbent doped with copper fat metal is 9 in number.
/as'' and desorption is possible by reducing the pressure. In this case, a compressor for pressurization and a vacuum pump for depressurization and desorption are required.

発明の効果 従来装置では、残留COS〜5%の為に、低温CO変成
装置が設けられていたが、これをCO吸着塔におきかえ
ることによって、複雑なC0変成装置を高温のみにする
ことができ、全体でのメリットが大きい。また、高温C
O変成装置にて生成する熱エネルギーを吸着塔での吸着
時の冷却源、または脱着時の加熱源として使えるので、
熱紅済上きわめて有効である。更に、脱着ガス中のCO
は、高温CO変成装置で再び転化反応をさせることKな
るが、濃度の濃い純粋なCOを増すこととなり、反応効
率が高められ、効率上好ましい。
Effects of the Invention In conventional equipment, a low-temperature CO shift device was installed in order to keep the residual COS at ~5%, but by replacing this with a CO adsorption tower, the complicated CO shift device can be made only for high temperatures. , the overall benefits are great. Also, high temperature C
The thermal energy generated in the O shift converter can be used as a cooling source during adsorption in the adsorption tower or as a heating source during desorption.
It is extremely effective in treating fever. Furthermore, CO in the desorption gas
In this case, the conversion reaction is carried out again in a high-temperature CO converter, but this increases the concentration of pure CO, which improves the reaction efficiency, which is preferable in terms of efficiency.

従って、本発明装置は、総合的見地からきわめて有効な
システムと云う事ができる。
Therefore, the device of the present invention can be said to be an extremely effective system from a comprehensive standpoint.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は、本発明に係る燃料改質装置のフローの一部を
示す。 復代理人  内 1)  明 復代理人  萩 原 亮 − 第1図
FIG. 1 shows a part of the flow of a fuel reformer according to the present invention. Sub-Agents 1) Meifuku Agent Ryo Hagiwara - Figure 1

Claims (1)

【特許請求の範囲】[Claims] 炭化水素に水蒸気を加えて水素へ改質する装置において
、高温CO変成装置の出口にCO吸着塔を設け、該CO
吸着塔の脱ガス工程では、脱ガスを該CO変成装置の入
口側に供給する手段を備えたことを特徴とする燃料改質
装置。
In a device that adds steam to hydrocarbons to reform them into hydrogen, a CO adsorption tower is installed at the outlet of the high-temperature CO shift device, and the CO
A fuel reformer characterized in that, in the degassing step of the adsorption tower, means is provided for supplying degas to the inlet side of the CO shift converter.
JP12736384A 1984-06-22 1984-06-22 Device for modifying fuel Pending JPS6110003A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12736384A JPS6110003A (en) 1984-06-22 1984-06-22 Device for modifying fuel

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12736384A JPS6110003A (en) 1984-06-22 1984-06-22 Device for modifying fuel

Publications (1)

Publication Number Publication Date
JPS6110003A true JPS6110003A (en) 1986-01-17

Family

ID=14958105

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12736384A Pending JPS6110003A (en) 1984-06-22 1984-06-22 Device for modifying fuel

Country Status (1)

Country Link
JP (1) JPS6110003A (en)

Similar Documents

Publication Publication Date Title
JP5796672B2 (en) How to operate a blast furnace or steelworks
US7763086B2 (en) Hydrogen purification process and system
JPH01313301A (en) Continuous production of hydrogen and carbon dioxide
WO2019073867A1 (en) Methane producing system
WO2020233030A1 (en) Device and method for synergistic recover of sulfur and hydrogen resources from hydrogen sulfide acid gas
JPH05306101A (en) Hydrogen production
JP2018071894A (en) Method for separating and recovering hydrogen from blast furnace gas, method for producing hydrogen, and separation and recovery system of hydrogen from blast furnace gas
JP2012148912A (en) Refining method and refining device of helium gas
JP5683390B2 (en) Helium gas purification method and purification apparatus
JP5748272B2 (en) Helium gas purification method and purification apparatus
JP2003165707A (en) Method and apparatus for manufacturing hydrogen
JP5665120B2 (en) Argon gas purification method and purification apparatus
JP5403685B2 (en) Argon gas purification method and purification apparatus
JPH10273301A (en) Hydrogen manufacturing equipment
JPS6110003A (en) Device for modifying fuel
CN211644593U (en) Based on CO before burning2Isothermal conversion system of trapping system
JP2000233918A (en) Production of carbon monoxide
JPH04325401A (en) Method and equipment for producing gaseous hydrogen
JP4313882B2 (en) Method for removing organic impurities in methanol decomposition gas by closed TSA method
JPS6110002A (en) Device for modifying fuel
JP5676995B2 (en) Waste heat energy recovery utilization method and recovery utilization system
CN218853934U (en) Carbon dioxide adjustable system for preparing reducing gas of shaft furnace by coke oven gas
JP2002274811A (en) Hydrogen preparation process and device used for the same
JP5255896B2 (en) Hydrogen production method
JP2000219508A (en) Production of co from off-gas in hydrogen pressure swing adsorption (psa)