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JPH05287284A - Process for reforming liquefied natural gas - Google Patents

Process for reforming liquefied natural gas

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Publication number
JPH05287284A
JPH05287284A JP8367092A JP8367092A JPH05287284A JP H05287284 A JPH05287284 A JP H05287284A JP 8367092 A JP8367092 A JP 8367092A JP 8367092 A JP8367092 A JP 8367092A JP H05287284 A JPH05287284 A JP H05287284A
Authority
JP
Japan
Prior art keywords
gas
liquefied natural
natural gas
lng
reforming
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
JP8367092A
Other languages
Japanese (ja)
Inventor
Yoshiyuki Takeuchi
竹内  善幸
Kiichiro Ogawa
紀一郎 小川
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 JP8367092A priority Critical patent/JPH05287284A/en
Publication of JPH05287284A publication Critical patent/JPH05287284A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To obtain efficiently a gas turbine fuel which does not evolve CO2 during combustion by reforming liquefied natural gas successively in a reformer and by the shift reaction, separating CO2 from the reformed gas, and liquefying the CO2 by the cold heat of the liquefied natural gas. CONSTITUTION:After the recovery of the cold heat of liquefied natural gas (hereinafter referred to an LNG) in cold-heat-recovery heat-exchangers 1 and 2, the LNG is gasified in an LNG vaporizer 3 and fed to a reformer 4. Steam is fed to the reformer 4 at the same time to reform CH4 in the feed gas to H2 and CO. Then, the reformed gas is introduced into a high-temperature CO shift reactor 5 and a low-temperature shift reactor 6 to reform the CO through the shift reaction with steam to H2 and CO2. Thereafter, the reformed gas is fed into PSA11 for CO2 absorption to separate and remove the CO2 which is then liquefied in a CO2 liquefier 13 making use of the cold heat of the LNG. On the other hand, the reformed gas, from which CO2 has been separated, is used as a fuel in a gas turbine 15.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は液化天然ガスの改質方法
に関する。
FIELD OF THE INVENTION The present invention relates to a method for reforming liquefied natural gas.

【0002】[0002]

【従来の技術】従来、燃焼排ガス中の一部の炭酸ガスを
濃縮し、気体、液体または固体状で分離・回収していた
が、実質的には当該炭酸ガスの回収をほとんどおこなっ
ておらず、そのまま大気へ放出していた。これらの大気
中に放出された炭酸ガスの1/2は海洋等に吸収され、
残りは大気中に残存することや、近年の燃焼排ガスの量
の増加とあいまって、海洋等の吸収では追いつかない状
態にある。従って、大気中の炭酸ガス量が増加し、近
年、温室効果と呼ばれている大気温度の上昇が問題視さ
れることとなった。
2. Description of the Related Art Conventionally, a part of carbon dioxide gas in combustion exhaust gas has been concentrated and separated and collected in a gas, liquid or solid state, but the carbon dioxide gas is practically not collected. , Was released to the atmosphere as it was. Half of the carbon dioxide released into the atmosphere is absorbed by the ocean,
The rest remains in the atmosphere, and due to the increase in the amount of combustion exhaust gas in recent years, absorption by the ocean etc. cannot keep up. Therefore, the amount of carbon dioxide in the atmosphere has increased, and in recent years, an increase in atmospheric temperature called the greenhouse effect has become a problem.

【0003】炭酸ガスを分離する方法として、吸収法と
吸着法がある。表1に吸収法の例を示す。一般に加圧に
より炭酸ガスを吸収液に吸収し、再生工程で圧力を低下
するか加熱して吸収液の再生を行う。
As a method for separating carbon dioxide gas, there are an absorption method and an adsorption method. Table 1 shows an example of the absorption method. Generally, carbon dioxide gas is absorbed into the absorbing solution by pressurization, and the absorbing solution is regenerated by lowering the pressure or heating in the regeneration step.

【0004】[0004]

【表1】 [Table 1]

【0005】吸着法も加圧により吸着剤に炭酸ガスを吸
着させ、再生工程で減圧して吸着剤の再生を行う。この
吸着・再生工程は非連続的であり、圧力・温度の変化を
伴う。
In the adsorption method as well, carbon dioxide gas is adsorbed on the adsorbent by pressurization, and the adsorbent is regenerated by reducing the pressure in the regeneration step. This adsorption / regeneration process is discontinuous and involves changes in pressure and temperature.

【0006】一方、最近では天然ガスを液化して輸送・
貯蔵し、これを燃料として用いた高効率ガスタービン複
合発電による発電所の建設が推進されており、この液化
天然ガス(LNG)をガス燃料として利用する際に放出
されるLNGの保有する冷熱を用いて炭酸ガスをドライ
アイスとして固化・回収する方法が提案されている。
On the other hand, recently, natural gas is liquefied and transported.
The construction of a power plant by high-efficiency gas turbine combined power generation that stores and uses this as fuel is being promoted. The cold heat of LNG released when this liquefied natural gas (LNG) is used as gas fuel is being promoted. A method of solidifying and recovering carbon dioxide as dry ice by using it has been proposed.

【0007】特開昭61−40808に提案されている
方法は低温の液化天然ガスを二酸化炭素冷却器(熱交換
器)内に設けられた冷却パイプ内に供給し、該冷却パイ
プ外部に炭酸ガスを含有する排ガスを流通する。この際
に、冷却パイプ内の低温の液化天然ガスの冷熱により、
冷却パイプ外の炭酸ガスが間接熱交換されて冷却され、
パイプ表面に固化して付着する。これを時々掻き落とし
て集める。
In the method proposed in Japanese Patent Laid-Open No. 61-40808, low temperature liquefied natural gas is supplied into a cooling pipe provided in a carbon dioxide cooler (heat exchanger), and carbon dioxide gas is provided outside the cooling pipe. Exhaust gas containing is distributed. At this time, due to the cold heat of the low temperature liquefied natural gas in the cooling pipe,
Carbon dioxide gas outside the cooling pipe is cooled by indirect heat exchange,
It solidifies and adheres to the pipe surface. This is sometimes scraped off and collected.

【0008】また、LNGの冷熱と熱交換して低温に冷
却されたガスと炭酸ガスを含有する排ガスを直接混合す
ることにより、炭酸ガスを固化・分離する方法の提案も
ある。
There is also a proposal of a method for solidifying and separating carbon dioxide gas by directly mixing the gas cooled to a low temperature by exchanging heat with the cold heat of LNG and the exhaust gas containing carbon dioxide gas.

【0009】[0009]

【発明が解決しようとする課題】燃焼排ガス中の炭酸ガ
ス濃度は非常に低く、約5〜10モル%であり、多量の
ガス中から微量のCO2 を分離・回収する方法では非常
にエネルギ効率が悪く、技術的にも非常に困難である。
The concentration of carbon dioxide gas in the combustion exhaust gas is very low, about 5 to 10 mol%, and the method of separating and recovering a minute amount of CO 2 from a large amount of gas is very energy efficient. Is bad and technically very difficult.

【0010】本発明は上記技術水準に鑑み、CO2 の発
生を抑制すると共に発生したCO2を合目的に回収しう
る方法を提供しようとするものである。
The present invention seeks to provide a process capable of recovering CO 2 generated with consideration of the above prior art, to suppress the occurrence of CO 2 expediently.

【0011】[0011]

【課題を解決するための手段】本発明は液化天然ガスを
ガスタービン用燃料として改質する方法にいて、液化天
然ガスをリフォーマによりH2 及びCOを主成分とする
ガスに改質し、さらにCOをスチームとのシフト反応に
よりH2 とCO2 に改質した後、該改質ガスから分離・
除去したCO2 を液化天然ガスが保有する冷熱により液
化することを特徴とする液化天然ガスの改質方法であ
る。
The present invention relates to a method for reforming liquefied natural gas as a fuel for a gas turbine, wherein the liquefied natural gas is reformed by a reformer into a gas containing H 2 and CO as main components, and further, After reforming CO into H 2 and CO 2 by a shift reaction with steam, it is separated from the reformed gas.
A method for reforming liquefied natural gas, characterized in that the removed CO 2 is liquefied by the cold heat possessed by the liquefied natural gas.

【0012】以下、本発明について、図1を参照してよ
り具体的に説明する。LNGは一般に約−160〜−1
70℃の低温で発電所に輸送されてくる。該LNGの保
有する冷熱を冷熱回収用熱交換器1及び2で熱回収した
後、LNG気化器3で液状から気体状に気化してリフォ
ーマ4に供給する。
Hereinafter, the present invention will be described more specifically with reference to FIG. LNG is generally about -160 to -1
It is transported to the power plant at a low temperature of 70 ℃. After the cold heat held by the LNG is recovered by the heat recovery heat exchangers 1 and 2, the LNG vaporizer 3 vaporizes it from liquid to gas and supplies it to the reformer 4.

【0013】一方、該リフォーマ4にはスチームが供給
され、約800〜900℃で以下の反応により原料ガス
中のCH4 の約80%以上がH2 とCOに改質される。 CH4 + H2 O → 3H2 + CO さらに、改質ガスは高温COシフト反応器5及び低温C
Oシフト反応器6に導かれ、約300〜400℃で以下
の反応によりH2 とCO2 に改質される。 CO + H2 O → H2 + CO2
On the other hand, steam is supplied to the reformer 4, and about 80% or more of CH 4 in the raw material gas is reformed into H 2 and CO by the following reaction at about 800 to 900 ° C. CH 4 + H 2 O → 3H 2 + CO Further, the reformed gas is a high temperature CO shift reactor 5 and a low temperature C
It is introduced into the O shift reactor 6 and reformed into H 2 and CO 2 by the following reaction at about 300 to 400 ° C. CO + H 2 O → H 2 + CO 2

【0014】改質ガスは廃熱回収ボイラ7、ガス冷却器
8で熱回収の後、ドレンセパレータ9及び除湿用PSA
10でH2 Oを分離・除去してCO2 分離用PSA11
に導かれる。ここで、改質ガス中のCO2 及び未改質の
CH4 が分離されて、コンプレッサ12で約20kg/
cm2 以上に加圧後、CO2 液化装置13で気体から液
体に相変化した後液体として貯蔵タンク14に回収され
る。
After the heat of the reformed gas is recovered by the waste heat recovery boiler 7 and the gas cooler 8, the drain separator 9 and the PSA for dehumidification are used.
PSA for CO 2 separation by separating and removing H 2 O at 10
Be led to. Here, the CO 2 and the unreformed CH 4 in the reformed gas are separated and about 20 kg /
After being pressurized to cm 2 or more, the CO 2 liquefaction device 13 changes the phase from a gas to a liquid and is then recovered in the storage tank 14 as a liquid.

【0015】一方、CO2 及び未改質のCH4 を分離し
た後のH2 を主成分とする改質ガスはガスタービン15
で燃料として使用される。この時発生するガスはH2
のみである。 H2 + O2 → H2
On the other hand, the reformed gas containing H 2 as a main component after separating CO 2 and unreformed CH 4 from the gas turbine 15
Used as fuel in. The gas generated at this time is H 2 O
Only. H 2 + O 2 → H 2 O

【0016】ガスタービン排出ガスは、さらにスチーム
タービン16および発熱回収熱交換器17で廃熱を回収
した後、煙突18から排出される。
The exhaust gas from the gas turbine is further discharged from the chimney 18 after the waste heat is recovered by the steam turbine 16 and the heat recovery heat exchanger 17.

【0017】以上の方法により、原料中の炭素を直接燃
焼せずに改質により液状のCO2 として分離・回収した
後の炭素を含まないガスを燃料として使用する。
By the above method, the carbon-free gas after the carbon in the raw material is separated and recovered as liquid CO 2 by reforming without directly burning it is used as the fuel.

【0018】[0018]

【作用】(1)LNGの主成分はCH4 であり、H2
とのリフォーミング反応により炭素をCOに改質する。 CH4 + H2 O → 3H2 + CO (2)COとH2 Oの改質反応によりH2 とCO2 を生
成する。 CO + H2 O → H2 + CO2 (3)生成したCO2 をPSAにより燃料ガス(H2
から分離・除去する。一般に空気を使用してLNGを直
接燃焼する場合に対して、燃焼排ガス中にN 2 を含有し
ないのでCO2 濃度が高く、CO2 分離エネルギが少な
い。 (4)H2 の燃焼反応ではCO2 が生成しない。従っ
て、燃焼排ガス中にCO2は混入しない。 H2 + O2 → H2
[Operation] (1) The main component of LNG is CHFourAnd H2O
Reforms carbon to CO by reforming reaction with. CHFour+ H2O → 3H2+ CO (2) CO and H2O reforming reaction causes H2And CO2Live
To achieve. CO + H2O → H2 + CO2 (3) Generated CO2Fuel gas (H2)
To remove from. Generally, air is used to correct LNG.
Compared to the case of direct combustion, N in the combustion exhaust gas 2Contains
Because there is no CO2High concentration, CO2Low separation energy
Yes. (4) H2In the combustion reaction of CO2Does not generate. Obey
CO in the combustion exhaust gas2Does not mix. H2 + O2 → H2O

【0019】[0019]

【実施例】図1に示した本発明のプロセスフローによっ
て行った1,400MW規模のプラントの物質収支例を
表2に示す。表1の項目中の〜は図1中に示した個
所を示す。
EXAMPLE Table 2 shows an example of the material balance of a plant of 1,400 MW scale, which was carried out by the process flow of the present invention shown in FIG. In Table 1, items 1 to 3 indicate the points shown in FIG.

【0020】[0020]

【表2】 [Table 2]

【0021】[0021]

【発明の効果】以上、説明したように本発明は(1)原
料中の炭素を高濃度の状態で分離・除去するために炭素
の分離効率がよく、(2)さらに改質反応で生成したH
2 の燃焼ではCO2 が発生しないため、現在地球環境汚
染で問題となっているCO2 の発生が無いなどの特徴が
あり、工業規模の装置に有利に適用しうる方法である。
As described above, according to the present invention, (1) the carbon in the raw material is separated and removed in a high concentration state, so that the carbon separation efficiency is good, and (2) the carbon is produced by the reforming reaction. H
Since CO 2 is not generated in the combustion of No. 2, there is a feature that there is no generation of CO 2 which is currently a problem in global environmental pollution, and this method can be advantageously applied to an industrial scale device.

【図面の簡単な説明】[Brief description of drawings]

【図1】本発明の方法を示すプロセスの一実施例の系統
図。
FIG. 1 is a flow chart of one embodiment of a process showing the method of the present invention.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 液化天然ガスをガスタービン用燃料とし
て改質する方法にいて、液化天然ガスをリフォーマによ
りH2 及びCOを主成分とするガスに改質し、さらにC
Oをスチームとのシフト反応によりH2 とCO2 に改質
した後、該改質ガスから分離・除去したCO2 を液化天
然ガスが保有する冷熱により液化することを特徴とする
液化天然ガスの改質方法。
1. A method for reforming liquefied natural gas as a fuel for a gas turbine, wherein the liquefied natural gas is reformed by a reformer into a gas containing H 2 and CO as main components, and C
After reforming the H 2 and CO 2 by a shift reaction with steam to O, liquefied natural gas, characterized in that the liquefied by cold energy possessed by the CO 2 liquefied natural gas separated and removed from the reforming gas Modification method.
JP8367092A 1992-04-06 1992-04-06 Process for reforming liquefied natural gas Pending JPH05287284A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8367092A JPH05287284A (en) 1992-04-06 1992-04-06 Process for reforming liquefied natural gas

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8367092A JPH05287284A (en) 1992-04-06 1992-04-06 Process for reforming liquefied natural gas

Publications (1)

Publication Number Publication Date
JPH05287284A true JPH05287284A (en) 1993-11-02

Family

ID=13808915

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8367092A Pending JPH05287284A (en) 1992-04-06 1992-04-06 Process for reforming liquefied natural gas

Country Status (1)

Country Link
JP (1) JPH05287284A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0943585A3 (en) * 1998-03-17 2000-05-03 Kabushiki Kaisha Toshiba Combustion system
EP1267432A3 (en) * 2001-06-15 2005-03-30 Chart, Inc. Fuel cell refueling station and system
JP2007031255A (en) * 2005-07-29 2007-02-08 Toshiba Corp Low quality waste heat recovery system
JP2007031256A (en) * 2005-07-29 2007-02-08 Toshiba Corp Hydrogen production system
WO2008041076A2 (en) * 2006-10-03 2008-04-10 L'air Liquide-Societe Anonyme Pour L'etude Et L'exploitation Des Procedes Georges Claude Steam methane reforming with lng regasification terminal for lng vaporization
JP2011102538A (en) * 2009-11-10 2011-05-26 Hitachi Ltd Gasification power generation system equipped with carbon dioxide separation and recovery device

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0943585A3 (en) * 1998-03-17 2000-05-03 Kabushiki Kaisha Toshiba Combustion system
EP1267432A3 (en) * 2001-06-15 2005-03-30 Chart, Inc. Fuel cell refueling station and system
JP2007031255A (en) * 2005-07-29 2007-02-08 Toshiba Corp Low quality waste heat recovery system
JP2007031256A (en) * 2005-07-29 2007-02-08 Toshiba Corp Hydrogen production system
JP4744971B2 (en) * 2005-07-29 2011-08-10 株式会社東芝 Low quality waste heat recovery system
WO2008041076A2 (en) * 2006-10-03 2008-04-10 L'air Liquide-Societe Anonyme Pour L'etude Et L'exploitation Des Procedes Georges Claude Steam methane reforming with lng regasification terminal for lng vaporization
WO2008041076A3 (en) * 2006-10-03 2009-07-02 Air Liquide Steam methane reforming with lng regasification terminal for lng vaporization
US7849691B2 (en) 2006-10-03 2010-12-14 Air Liquide Process & Construction, Inc. Steam methane reforming with LNG regasification terminal for LNG vaporization
JP2011102538A (en) * 2009-11-10 2011-05-26 Hitachi Ltd Gasification power generation system equipped with carbon dioxide separation and recovery device
EP2320049A3 (en) * 2009-11-10 2017-06-21 Mitsubishi Hitachi Power Systems, Ltd. Gasification power generation system provided with carbon dioxide separation and recovery device

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