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JPH11116508A - Treatment for transforming carbon dioxide into organic material - Google Patents

Treatment for transforming carbon dioxide into organic material

Info

Publication number
JPH11116508A
JPH11116508A JP9278615A JP27861597A JPH11116508A JP H11116508 A JPH11116508 A JP H11116508A JP 9278615 A JP9278615 A JP 9278615A JP 27861597 A JP27861597 A JP 27861597A JP H11116508 A JPH11116508 A JP H11116508A
Authority
JP
Japan
Prior art keywords
water
carbon dioxide
hydrogen
organic material
slurry
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.)
Granted
Application number
JP9278615A
Other languages
Japanese (ja)
Other versions
JP4044990B2 (en
Inventor
Nakamichi Yamazaki
仲道 山▲崎▼
Tomonori Yamazaki
友紀 山▲崎▼
Tokumi Satake
徳己 佐竹
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 JP27861597A priority Critical patent/JP4044990B2/en
Publication of JPH11116508A publication Critical patent/JPH11116508A/en
Application granted granted Critical
Publication of JP4044990B2 publication Critical patent/JP4044990B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/20Air quality improvement or preservation, e.g. vehicle emission control or emission reduction by using catalytic converters

Landscapes

  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

PROBLEM TO BE SOLVED: To provide a treating method for transforming carbon dioxide into an organic material, by which the carbon dioxide (CO2 ) is transformed into a reusable organic material by an industrially feasible method by reducing the carbon dioxide with hydrogen by a hydrothermal reaction by using an iron component as a catalyst, etc., and water as a hydrogen source under saturated steam pressure. SOLUTION: CO2 is supplied to a hopper 1 from a supplying line 2, and water of >=2 molar times as much as the number of moles of the CO2 is supplied from a water-supplying line 3. The supplied CO2 and water are formed into a aqueous solution state in a mixing line 4, and a pulverized slag consisting essentially of FeO, etc., is fed to the mixture in the aqueous solution state. The obtained mixture is kneaded by an agitator 9 to provide a slurry. The obtained slurry coming through a valve 10 is pressurized by a slurry pump 5 to 100-400 atm, and introduced into a reaction tube 7 at a temperature kept by a heater 6. A hydrothermal reaction of the slurry is carried out in the reaction tube 7 at about 300-400 deg.C under a saturated steam pressure to reduce the CO2 with hydrogen to provide an organic material such as methanol and propane.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、火力発電等の化石
燃料を燃焼することにより発生する二酸化炭素(C
2 )を有機物化する方法に関するもので、とくにCO
2 を、燃料として再資源化する方法に関する。
The present invention relates to carbon dioxide (C) generated by burning fossil fuels for thermal power generation and the like.
O 2 ) to organic matter, especially CO 2
2 as a fuel.

【0002】[0002]

【従来の技術】従来、地球温暖化防止の手法として、C
2 を回収し、これを固定化もしくは再利用する研究が
行なわれている。その代表例として、回収したCO2
クラスレート化して海中に固定する方法、あるいは藻類
や微生物を利用したバイオマスによってCO2 を固定し
て再資源化を図ることが提案されている。また、CO2
を原料とし、触媒を用いてこれからメタンや水素を生成
する方法なども提案されている。
2. Description of the Related Art Conventionally, as a method of preventing global warming, C
The O 2 was recovered, fixed or reused studies have been made to this. As a typical example, a method has been proposed in which the recovered CO 2 is clathrated and fixed in the sea, or the CO 2 is fixed by biomass utilizing algae or microorganisms to achieve recycling. CO 2
There has been proposed a method of producing methane and hydrogen from a raw material using a catalyst and a catalyst.

【0003】しかし、これらは研究の緒についたばかり
であり、クラスレート化による固定については、海中環
境の問題が新たにクローズアップされており、クラスレ
ート化するためのエネルギー消費等、経済性に対する問
題が指摘されている。また、バイオマスによる処理につ
いては、大量生産(処理)に難点があるとの指摘もあ
る。さらに、触媒水素化法により、CO2 からメタンや
水素を生成させる方法は、現在、最も期待されている
が、CO2 の化学転換に要するエネルギーが高くなる可
能性があり、これら何れの方法も経済的に懸念があり、
産業ベースに乗る具体案がないのが現状である。
[0003] However, these are just the beginning of research, and with regard to fixation by clathrating, the problem of the marine environment has been newly highlighted, and problems with economic efficiency such as energy consumption for clathrating. Has been pointed out. It has also been pointed out that there is a problem in mass production (processing) with respect to processing using biomass. Furthermore, the method of producing methane and hydrogen from CO 2 by catalytic hydrogenation is currently the most promising, but the energy required for chemical conversion of CO 2 may be high. Financially concerned,
At present, there is no specific plan for riding on an industrial basis.

【0004】[0004]

【発明が解決しようとする課題】本発明は産業的に成り
立つ手法で、CO2 を有機物化し、これを資源として再
利用を図り得る方法を提供することを目的とする。
SUMMARY OF THE INVENTION It is an object of the present invention to provide a method for converting CO 2 into organic matter and reusing it as a resource by an industrially feasible method.

【0005】[0005]

【課題を解決するための手段】本発明は、上記課題を解
決しようとするもので、その要旨は、二酸化炭素を、鉄
成分を触媒もしくは反応材として、水を水素源とした飽
和水蒸気圧の下で水熱反応による水素還元を行い、有機
化合物を得ることを特徴とする二酸化炭素の有機物化処
理方法を提供するものである。
SUMMARY OF THE INVENTION The present invention aims to solve the above-mentioned problems. The gist of the present invention is to use carbon dioxide as an iron component as a catalyst or a reactant, and a saturated steam pressure using water as a hydrogen source. An object of the present invention is to provide a method for organically converting carbon dioxide, which comprises performing hydrogen reduction by a hydrothermal reaction below to obtain an organic compound.

【0006】[0006]

【発明の実施の形態】本発明は、CO2 を水素還元して
有機物化し、CO2 を資源化する。このため、水を水素
源とした飽和水蒸気圧下で、CO2 を、鉄成分を触媒も
しくは吸着材として水素反応させる。鉄成分としては、
Fe0 ,FeO,Fe3 4 を用いることができる。本
実施例では例えば鉱滓を用いた。鉱滓はFeO,Fe3
4 を主成分としているが、上記反応によってヘマタイ
ト(Fe2 3 )化する。ヘマタイト化した鉱滓は、こ
れを高炉へ戻してやれば、そのまま製鉄する上での原材
料となり、資源的にロスとはならない。鉱滓は、そのF
e成分が触媒として働く。水素還元を行うに当っては、
水をそのまま水素源とするため、水素等を用いるものに
比べ遙に安価な溶媒となる。
BEST MODE FOR CARRYING OUT THE INVENTION In the present invention, CO 2 is hydrogenated to be converted into an organic substance and CO 2 is recycled. Therefore, under a saturated steam pressure using water as a hydrogen source, CO 2 is hydrogen-reacted using an iron component as a catalyst or an adsorbent. As the iron component,
Fe 0 , FeO, and Fe 3 O 4 can be used. In this embodiment, for example, slag is used. Slag is FeO, Fe 3
Although O 4 is a main component, it is converted into hematite (Fe 2 O 3 ) by the above reaction. If hematite slag is returned to the blast furnace, it will be used as a raw material for steelmaking as it is, and will not be a resource loss. The slag is its F
The component e works as a catalyst. In performing hydrogen reduction,
Since water is used as a hydrogen source as it is, it is a much cheaper solvent than one using hydrogen or the like.

【0007】エネルギーの面からみると、水熱反応する
ために飽和水蒸気圧の環境を維持するだけで済み、かつ
CO2 とFeO/Fe3 4 との反応が発熱反応である
ことから、この点においても有利である。本発明によれ
ば、エネルギー的ロス、資源的ロスを少くして、CO2
を容易にエネルギー源として再利用することができる。
従来のCO2 の処理方法に対し、より経済性の高い方法
を提供することができる。
From the viewpoint of energy, it is only necessary to maintain an environment of a saturated steam pressure for hydrothermal reaction, and the reaction between CO 2 and FeO / Fe 3 O 4 is an exothermic reaction. It is also advantageous in point. According to the present invention, energy loss and resource loss are reduced and CO 2
Can be easily reused as an energy source.
It is possible to provide a more economical method than the conventional CO 2 treatment method.

【0008】図1を参照しながら、本発明を詳細に説明
すると、ホッパ1の中へCO2 供給ライン2からCO2
を、水供給ライン3から水を供給し、混合ライン4でC
2を水溶液化した状態にしてホッパ1に送り込む。次
いでホッパ1の中へ、さらにFeO及びFe2 3 を主
成分とする粉砕された鉱滓を送り、攪拌機9で混練しス
ラリー化する。CO2 ,水,鉱滓よりなるスラリー状物
は、バルブ10を通ってスラリーポンプ5により加圧さ
れ、ヒータ6で温度保持された反応管7に入り、ここで
300℃〜400℃程度の飽和水蒸気圧下で、水熱反応
が行われる。
[0008] With reference to FIG. 1, when describing the present invention in detail, CO 2 from the CO 2 supply line 2 into the hopper 1
Is supplied from a water supply line 3, and C is supplied through a mixing line 4.
O 2 is converted into an aqueous solution and sent to the hopper 1. Next, the pulverized slag mainly containing FeO and Fe 2 O 3 is fed into the hopper 1 and kneaded by a stirrer 9 to form a slurry. A slurry made of CO 2 , water, and slag is pressurized by a slurry pump 5 through a valve 10 and enters a reaction tube 7 maintained at a temperature by a heater 6, where it is saturated with steam of about 300 ° C. to 400 ° C. Under pressure, a hydrothermal reaction takes place.

【0009】そのさい、CO2 のモル数に対し、水は2
倍以上のモル数となるように加え、100〜400気圧
に加圧することが好ましい。このように、300℃〜4
00℃程度の飽和水蒸気圧下の水中にFeO,Fe3
4 を主成分とする鉱滓を混入し、その中へCO2 を送り
込むと、Feの触媒作用及びヘマタイト化への化合反応
を促進する作用により、CO2 は水素還元され、メタノ
ール(CH3 OH)やプロパン(CH3 CH2 CH3
等の有機物に転化される。
[0009] for that again, the number of moles of CO 2, water is 2
It is preferable that the pressure is increased to 100 to 400 atm in addition to the molar number twice or more. Thus, from 300 ° C. to 4
FeO, Fe 3 O in water under saturated steam pressure of about 00 ° C
When slag containing 4 as a main component is mixed and CO 2 is fed into the slag, CO 2 is reduced by hydrogen by the catalytic action of Fe and the action of promoting the compounding reaction to hematite formation, and methanol (CH 3 OH) And propane (CH 3 CH 2 CH 3 )
And so on.

【0010】上記水素還元は例えば、下式によって行な
われる。 CO2 +H2 O+Fex( )y → CH3 OH,
CH3 OCH3 等 式中( )内は、Fe0 ,FeO,Fe3 2 ,Fe
2 3 の混合物である。Fe0 はFe3+となって、水素
3個分、Fe2+Oは水素2個分、Fe3 4 は水素1個
分が各々CO2 を還元するように関与する。
The above-mentioned hydrogen reduction is carried out, for example, by the following formula. CO 2 + H 2 O + Fex () y → CH 3 OH,
CH 3 OCH 3, etc. In the parentheses, Fe 0 , FeO, Fe 3 O 2 , Fe
It is a mixture of 2 O 3 . Fe 0 becomes Fe 3+ , three hydrogen atoms, Fe 2+ O two hydrogen atoms, and Fe 3 O 4 one hydrogen atom so as to reduce CO 2 .

【0011】このように、鉱滓は触媒としての機能を持
つと共に、ヘマタイト化して化合反応を促進する作用を
し、これにより、水中の水素でCO2 を還元する。この
ときのGC/MS解析(マス分析)の結果を図2に示
す。aのピークはメタノールで、bはアセトアルデヒ
ド,cはプロパノールであり、有機化合物を生成してい
ることが分る。この他、300℃〜400℃の範囲内で
飽和水蒸気圧を変えると、メタン等の生成もできる。有
機物の生成にあたって、特にメタノールを合成したいと
する場合は、350℃近傍が有効な反応領域となる。
As described above, the slag has a function as a catalyst, and at the same time, has a function of promoting hematite to promote a compounding reaction, thereby reducing CO 2 with hydrogen in water. FIG. 2 shows the result of the GC / MS analysis (mass analysis) at this time. The peak a is methanol, b is acetaldehyde, and c is propanol, indicating that an organic compound is produced. In addition, when the saturated steam pressure is changed within the range of 300 ° C. to 400 ° C., methane and the like can be generated. In the case of producing organic substances, particularly when it is desired to synthesize methanol, the vicinity of 350 ° C. is an effective reaction region.

【0012】このように反応した有機物を含む水溶液
は、フィルタ8で鉱滓と分離され、次の蒸留塔等への反
応ラインへ導かれ、所定の有機物と水に分離される。分
離された鉱滓は殆どがヘマタイト化されているため、溶
鉱炉で鉱材として用いるか、あるいは、H2 もしくはC
O等の水性ガスにより、200℃前後の水熱反応によ
り、マグネタイト化して再利用することができる。この
場合、反応管7をカートリッジ化して取り替え可能と
し、置き替えることもできる。
The aqueous solution containing the organic matter reacted in this way is separated from the slag by the filter 8 and led to the next reaction line to a distillation tower or the like, where it is separated into predetermined organic matter and water. Since most tailings separated has been hematite reduction, or used as a mineral material in a blast furnace, or, H 2 or C
It can be magnetized and reused by a hydrothermal reaction at about 200 ° C. with a water gas such as O. In this case, the reaction tube 7 can be replaced by a cartridge, and can be replaced.

【0013】[0013]

【実施例】水ホッパ1中へCO2 のモル数に対して2倍
以上のモル数となる水を混合ラインで水溶液化して供給
し、これに200メッシュ以下に粉砕された鉱滓を加
え、250〜400℃で100〜400気圧で反応を行
ったところ、CO2 を有機化することができた。
EXAMPLE Water, which is twice or more the number of moles of CO 2 , was converted into an aqueous solution through a mixing line and supplied to a water hopper 1, and slag pulverized to a mesh of 200 mesh or less was added thereto. When the reaction was carried out at 100 to 400 atm at 400 ° C., CO 2 was able to be made organic.

【0014】[0014]

【発明の効果】本発明によればエネルギー的ロス、資源
的ロスを少くしてCO2 を容易にエネルギー源として再
利用することができる。
According to the present invention, CO 2 can be easily reused as an energy source while reducing energy loss and resource loss.

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

【図1】本発明に係る処理方法のフロー図である。FIG. 1 is a flowchart of a processing method according to the present invention.

【図2】本発明に基づくGC/MC解析の結果を示す図
である。
FIG. 2 is a diagram showing the results of GC / MC analysis based on the present invention.

【符号の説明】[Explanation of symbols]

1 ホッパ 2 CO2 供給ライン 3 水供給ライン 4 混合ライン 5 スラリーポンプ 6 ヒータ 7 反応管 8 フィルタ 9 攪拌機 10 バルブ1 hopper 2 CO 2 supply line 3 water supply line 4 mixing line 5 slurry pump 6 heater 7 reaction tube 8 filter 9 agitator 10 valve

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 二酸化炭素を、鉄成分を触媒もしくは反
応材として、水を水素源とした飽和水蒸気圧下で水熱反
応により水素還元を行い、有機化合物を得ることを特徴
とする二酸化炭素の有機物化処理方法。
1. An organic substance of carbon dioxide, wherein hydrogen reduction is carried out by a hydrothermal reaction under a saturated steam pressure using water as a hydrogen source and carbon dioxide as an iron component as a catalyst or a reactant to obtain an organic compound. Treatment method.
JP27861597A 1997-10-13 1997-10-13 Carbon dioxide organic treatment method Expired - Fee Related JP4044990B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP27861597A JP4044990B2 (en) 1997-10-13 1997-10-13 Carbon dioxide organic treatment method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP27861597A JP4044990B2 (en) 1997-10-13 1997-10-13 Carbon dioxide organic treatment method

Publications (2)

Publication Number Publication Date
JPH11116508A true JPH11116508A (en) 1999-04-27
JP4044990B2 JP4044990B2 (en) 2008-02-06

Family

ID=17599755

Family Applications (1)

Application Number Title Priority Date Filing Date
JP27861597A Expired - Fee Related JP4044990B2 (en) 1997-10-13 1997-10-13 Carbon dioxide organic treatment method

Country Status (1)

Country Link
JP (1) JP4044990B2 (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010099626A (en) * 2008-10-27 2010-05-06 Mitsui Eng & Shipbuild Co Ltd Apparatus and method for reducing and fixing carbon dioxide
FR2973364A1 (en) * 2011-03-31 2012-10-05 IFP Energies Nouvelles METHOD FOR THE VALORISATION OF CO2
JP2017226624A (en) * 2016-06-23 2017-12-28 学校法人 名城大学 Method for producing hydrocarbons
CN109516892A (en) * 2018-11-29 2019-03-26 上海交通大学 The method for producing long chain alkane using iron powder and cobalt powder hydrothermal reduction carbon dioxide
JP2021006607A (en) * 2019-06-28 2021-01-21 国立研究開発法人産業技術総合研究所 Method for producing hydrocarbon
JP2023143189A (en) * 2022-03-25 2023-10-06 本田技研工業株式会社 Fuel manufacturing system

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010099626A (en) * 2008-10-27 2010-05-06 Mitsui Eng & Shipbuild Co Ltd Apparatus and method for reducing and fixing carbon dioxide
FR2973364A1 (en) * 2011-03-31 2012-10-05 IFP Energies Nouvelles METHOD FOR THE VALORISATION OF CO2
JP2017226624A (en) * 2016-06-23 2017-12-28 学校法人 名城大学 Method for producing hydrocarbons
CN109516892A (en) * 2018-11-29 2019-03-26 上海交通大学 The method for producing long chain alkane using iron powder and cobalt powder hydrothermal reduction carbon dioxide
CN109516892B (en) * 2018-11-29 2020-08-04 上海交通大学 Method for producing long-chain alkane by using iron powder and cobalt powder to hydrothermally reduce carbon dioxide
JP2021006607A (en) * 2019-06-28 2021-01-21 国立研究開発法人産業技術総合研究所 Method for producing hydrocarbon
JP2023143189A (en) * 2022-03-25 2023-10-06 本田技研工業株式会社 Fuel manufacturing system

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