JP5879091B2 - Combined thermal power generation system - Google Patents
Combined thermal power generation system Download PDFInfo
- Publication number
- JP5879091B2 JP5879091B2 JP2011233079A JP2011233079A JP5879091B2 JP 5879091 B2 JP5879091 B2 JP 5879091B2 JP 2011233079 A JP2011233079 A JP 2011233079A JP 2011233079 A JP2011233079 A JP 2011233079A JP 5879091 B2 JP5879091 B2 JP 5879091B2
- Authority
- JP
- Japan
- Prior art keywords
- facility
- power generation
- thermal power
- water
- hydrogen production
- 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 - Fee Related
Links
Images
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
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E20/00—Combustion technologies with mitigation potential
- Y02E20/16—Combined cycle power plant [CCPP], or combined cycle gas turbine [CCGT]
-
- 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
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/30—Hydrogen technology
- Y02E60/36—Hydrogen production from non-carbon containing sources, e.g. by water electrolysis
-
- 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
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
-
- 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
- Y02T—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
- Y02T10/00—Road transport of goods or passengers
- Y02T10/10—Internal combustion engine [ICE] based vehicles
- Y02T10/12—Improving ICE efficiencies
Landscapes
- Engine Equipment That Uses Special Cycles (AREA)
- Catalysts (AREA)
- Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
Description
本発明は、火力発電設備における燃焼に伴って発生する窒素酸化物(以下NOx)の大気への排出を低減させることができる複合型発電システムに関する。 The present invention relates to a combined power generation system that can reduce the emission of nitrogen oxides (hereinafter referred to as NOx) generated with combustion in a thermal power generation facility to the atmosphere.
火力発電設備において、燃料燃焼時には燃料含有窒素N成分に起因するフューエルNOx、窒素存在(空気)雰囲気下における高温燃焼に起因するサーマルNOxが発生する。NOxは酸性雨の原因となることやその毒性などから排出抑制が望まれ、排出規制が設けられているガスである。 In a thermal power generation facility, fuel NOx resulting from fuel-containing nitrogen N component and thermal NOx resulting from high-temperature combustion in a nitrogen presence (air) atmosphere are generated during fuel combustion. NOx is a gas for which emission control is desired because it causes acid rain and its toxicity, and has emission regulations.
NOx発生を低減させるために、例えば、燃料燃焼条件を低温にするなどして調節し燃焼効率を少し低下させて対応するなど、様々な対策がとられている(非特許文献1、2)。
In order to reduce the generation of NOx, various measures are taken, for example, by adjusting the fuel combustion condition by lowering the temperature to reduce the combustion efficiency (
火力発電設備から排出されるNOxを原料として有効利用することができれば、同時にNOxの排出の抑制も図ることができるので、そのシステムは理想的である。 If NOx discharged from a thermal power generation facility can be effectively used as a raw material, it is possible to suppress NOx emission at the same time, so that the system is ideal.
本発明は、上記事情に鑑みてなされたものであり、火力発電設備からのNOx排出を抑制することができる複合型火力発電システムを提供することを目的とする。 This invention is made | formed in view of the said situation, and it aims at providing the combined thermal power generation system which can suppress NOx discharge | emission from a thermal power generation equipment.
上記課題を解決するため、本発明の複合型火力発電システムは、火力発電設備と、水分解光触媒水素製造設備と、該火力発電設備から排出されるNOxと必要に応じて導かれる窒素、および該水分解光触媒水素製造設備で生成する水素を原料として利用してアンモニアを合成する化学合成設備とを有することを特徴とするものである。 In order to solve the above problems, a combined thermal power generation system of the present invention includes a thermal power generation facility, a water-splitting photocatalytic hydrogen production facility, NOx discharged from the thermal power generation facility, nitrogen introduced as necessary, and the And a chemical synthesis facility for synthesizing ammonia by using hydrogen generated in the water-splitting photocatalytic hydrogen production facility as a raw material.
上記複合型火力発電システムにおいて、好ましくは、前記火力発電設備からの排出蒸気を熱源として利用する海水淡水化設備をさらに有し、該海水淡水化設備で製造された水が前記水分解光触媒水素製造設備に供給される。 Preferably, the combined thermal power generation system further includes a seawater desalination facility that uses exhaust steam from the thermal power generation facility as a heat source, and water produced by the seawater desalination facility is the water-splitting photocatalytic hydrogen production Supplied to the facility.
好ましくは、前記化学合成設備で副生成する水が、前記水分解光触媒水素製造設備に供給される。 Preferably, water by-produced in the chemical synthesis facility is supplied to the water splitting photocatalytic hydrogen production facility.
本発明の複合型火力発電システムでは、化学合成設備において、火力発電設備から排出されるNOxと必要に応じて導かれる窒素、および該水分解光触媒水素製造設備で生成する水素を原料として利用してアンモニアが合成される。アンモニアは貯蔵・輸送されて、別途有効に利用される。本発明では、火力発電設備で排出されるNOxをアンモニア合成の原料とすることが可能となり、NOxを排出しないクリーンな複合型火力発電システムを形成することができる。また、本発明では、NOxのN成分がアンモニアとなり化学エネルギーとして有効に利用される。さらに、本発明のシステムを構築することで火力発電設備において排ガス脱硝設備が不要となり、設備のコンパクト化に繋がる。 In the combined thermal power generation system of the present invention, in the chemical synthesis facility, NOx discharged from the thermal power generation facility, nitrogen introduced as necessary, and hydrogen generated in the water splitting photocatalytic hydrogen production facility are used as raw materials. Ammonia is synthesized. Ammonia is stored and transported for effective use separately. In the present invention, NOx discharged from the thermal power generation facility can be used as a raw material for ammonia synthesis, and a clean combined thermal power generation system that does not discharge NOx can be formed. In the present invention, the N component of NOx becomes ammonia and is effectively used as chemical energy. Furthermore, the construction of the system of the present invention eliminates the need for exhaust gas denitration equipment in the thermal power generation equipment, leading to downsizing of the equipment.
火力発電設備で使用する燃料の違い(LNG、石炭)による排出NOx成分および量の差異は、その発電設備の規模を変更することで対応し、また必要量の窒素を適宜追加することにより、生成水素量を全量アンモニアに変換することが可能である。 The difference in NOx composition and quantity due to the difference in fuel used in thermal power generation equipment (LNG, coal) can be dealt with by changing the scale of the power generation equipment, and it can be generated by adding the required amount of nitrogen as appropriate. It is possible to convert the total amount of hydrogen to ammonia.
また、化学合成設備で副生成する水は、上流の水分解光触媒水素製造設備に供給されて有効に再利用される。 In addition, water produced as a by-product in the chemical synthesis facility is supplied to the upstream water-splitting photocatalytic hydrogen production facility and effectively reused.
場合(設置環境)によっては海水炭水化設備が不要となり、当該設備のコンパクトが可能となる。 Depending on the case (installation environment), the seawater charcoal liquefaction facility becomes unnecessary, and the facility can be made compact.
NOxは全量がアンモニア原料として利用され得るため、サーマルNOx発生を低減させるための低温燃料などの工夫は不要となり、発電設備において燃料の燃焼効率を向上させることが可能となる。 Since the entire amount of NOx can be used as an ammonia raw material, a device such as a low-temperature fuel for reducing the generation of thermal NOx is not required, and the combustion efficiency of fuel can be improved in the power generation facility.
以下、本発明の複合型火力発電システムについて詳細に説明する。 Hereinafter, the combined thermal power generation system of the present invention will be described in detail.
(実施の形態1)
図1は、実施の形態1の複合型火力発電システムを説明するフローシートである。
(Embodiment 1)
FIG. 1 is a flow sheet illustrating the combined thermal power generation system according to the first embodiment.
本実施の形態1の複合型火力発電システムは、火力発電設備(1)と、水分解光触媒水素製造設備(2)と、化学合成設備(3)とを有し、化学合成設備(3)は、火力発電設備(1)から排出されるNOxと必要に応じて導かれる窒素、および水分解光触媒水素製造設備(2)で生成する水素を原料として利用してアンモニアを合成する。 The combined thermal power generation system of Embodiment 1 includes a thermal power generation facility (1), a water splitting photocatalytic hydrogen production facility (2), and a chemical synthesis facility (3). Then, ammonia is synthesized using NOx discharged from the thermal power generation facility (1), nitrogen introduced as necessary, and hydrogen produced in the water splitting photocatalytic hydrogen production facility (2) as raw materials.
火力発電設備(1)として、例えば、燃料を燃焼させたガスでタービンを回転させるガスタービンと、燃料燃焼の排熱回収ボイラで生成した蒸気でタービンを回転させる蒸気タービンとを有するコンバインドサイクル火力発電が挙げられる。なお、以降の実施の形態2とは異なり、本実施の形態1では、火力発電設備で排出されるNOxおよび発生した電力のみを利用する構成であるので、火力発電設備(1)における蒸気の利用は必須ではない。
As the thermal power generation facility (1), for example, a combined cycle thermal power generation including a gas turbine that rotates a turbine with gas obtained by burning fuel and a steam turbine that rotates the turbine with steam generated by a waste heat recovery boiler for fuel combustion Is mentioned. Note that unlike
図2は、コンバインドサイクル火力発電設備を説明する内部概略図である。 FIG. 2 is an internal schematic diagram illustrating a combined cycle thermal power generation facility.
コンバインドサイクル火力発電システムは、発電機(11)と、ガスタービン(12)と、蒸気タービン(13)とを有し、ガスタービン(12)には、空気圧縮機(14)からの圧縮空気と燃料(例えばLNG、石油など)とが導入され、燃料の燃焼によりガスタービン(12)が回転し、この回転により発電機(11)にて発電する。燃料燃焼後に生じるガスタービン(12)からの排気は、排熱回収ボイラ(15)に送られ、ここで、別途取り込んだ海水などとの熱交換により冷却され、脱硫・CO2除去装置(16)に送られる。 The combined cycle thermal power generation system includes a generator (11), a gas turbine (12), and a steam turbine (13). The gas turbine (12) includes compressed air from an air compressor (14). Fuel (for example, LNG, petroleum, etc.) is introduced, and the gas turbine (12) is rotated by the combustion of the fuel, and the generator (11) generates electric power by this rotation. Exhaust gas from the gas turbine (12) generated after fuel combustion is sent to an exhaust heat recovery boiler (15), where it is cooled by heat exchange with separately taken seawater and the like, and desulfurization / CO 2 removal device (16) Sent to.
脱硫・CO2除去装置(16)における排出ガスからのNOx分離は、アルカリ吸収方式、酸素燃焼方式などを用いて行われる(http:/www.hitachiyoron.com/2008/05/pdf/05a0.4.pdf参照)。アルカリ吸収方式は、排出ガス中のCO2をアミンなどのアルカリ吸収液に吸収させる方式である。アルカリ吸収液に吸収させられたCO2は加熱することにより高濃度に回収され、同時にアルカリ吸収液が再生される。酸素燃焼方式は、燃料(石炭など)を酸素で燃焼させて排ガスを循環させつつ、燃焼に必要な酸素を供給することでCO2と水分を主成分とする排ガス組成とし、CO2を圧縮・回収する方式である。 The NOx separation from the exhaust gas in the desulfurization / CO 2 removal device (16) is performed using an alkali absorption method, an oxyfuel combustion method, or the like (http: /www.hitachiyoron.com/2008/05/pdf/05a0.4). see .pdf). The alkali absorption method is a method in which CO 2 in the exhaust gas is absorbed by an alkali absorption liquid such as amine. The CO 2 absorbed in the alkali absorbing solution is recovered to a high concentration by heating, and at the same time, the alkali absorbing solution is regenerated. Oxyfuel combustion system, while fuel by burning (such as coal) with oxygen by circulating exhaust gas, and exhaust gas composition to the CO 2 and water as a main component by supplying oxygen necessary for combustion, and compression of CO 2 It is a method to collect.
脱硫・CO2除去装置(16)を通過した後、排ガスは、発電設備から排気される。この排気は、NOxを含んでいる。また、排熱回収ボイラ(15)に供給された海水などの水は、熱交換により蒸気となり、蒸気タービン(13)に送られて、蒸気タービン(13)を回転させ、その後、蒸気の状態で発電設備から出る。 After passing through the desulfurization / CO 2 removal device (16), the exhaust gas is exhausted from the power generation facility. This exhaust contains NOx. Further, water such as seawater supplied to the exhaust heat recovery boiler (15) is converted into steam by heat exchange and sent to the steam turbine (13) to rotate the steam turbine (13), and then in the state of steam. Get out of the power generation facility.
水分解光触媒水素製造設備(2)は、太陽光と光触媒の作用により水を水素と酸素に分解する設備である。 The water splitting photocatalytic hydrogen production facility (2) is a facility that decomposes water into hydrogen and oxygen by the action of sunlight and a photocatalyst.
図3に水分解光触媒水素製造設備(2)の概略図を示す。 FIG. 3 shows a schematic diagram of the water-splitting photocatalytic hydrogen production facility (2).
水分解光触媒水素製造設備(2)は、上部の陽極室(21)と、この陽極室(21)に一端側にて連結する下部の陰極室(22)とを備えている。陽極室(21)には、太陽光により酸素を生成させる触媒作用を有する陽極光触媒(例えば、TaON、Ta3N5、TiO2−xNx、BiVO4、WO3など)(23)が備えられ、陰極室(22)には、水素を生成させる触媒作用を有する陰極触媒(例えば、Ptなど)(24)が備えられている。 The water-splitting photocatalytic hydrogen production facility (2) includes an upper anode chamber (21) and a lower cathode chamber (22) connected to the anode chamber (21) at one end side. The anode chamber (21), the anode photocatalyst having a catalytic action to produce oxygen by sunlight (e.g., TaON, Ta 3 N 5, TiO 2-x N x, etc. BiVO 4, WO 3) (23) is provided The cathode chamber (22) is provided with a cathode catalyst (for example, Pt) (24) having a catalytic action for generating hydrogen.
水は、一端側上端から陽極室(21)に導入され、一端側の連通路から陰極室(22)に通り、他端側下端を介して水分解光触媒水素製造設備から出る。 Water is introduced into the anode chamber (21) from the upper end on one end side, passes from the communication path on one end side to the cathode chamber (22), and exits from the water-splitting photocatalytic hydrogen production facility via the lower end on the other end side.
発電設備からの電力が電源(25)に供給され、太陽光が照射されると、陽極光触媒(23)の触媒作用により、酸素が発生する。発生した酸素は、陽極室(21)中央部上端に設けられた通気孔(26)から排出される。また、陰極室(22)では、陰極触媒(24)の触媒作用により、水素が発生する。発生した水素は、陰極室(22)中央部の所定区間に設けられた区画(27)を経て、陰極室(22)の他端側から排出される。 When electric power from the power generation facility is supplied to the power source (25) and irradiated with sunlight, oxygen is generated by the catalytic action of the anode photocatalyst (23). The generated oxygen is discharged from a vent hole (26) provided at the upper center of the anode chamber (21). In the cathode chamber (22), hydrogen is generated by the catalytic action of the cathode catalyst (24). The generated hydrogen is discharged from the other end side of the cathode chamber (22) through a section (27) provided in a predetermined section at the center of the cathode chamber (22).
化学合成設備(3)には、火力発電設備(1)からのNOxおよび電力が供給され、水分解光触媒水素製造設備(2)から水素が供給され、これらを原料としてアンモニアが合成される。反応に用いられる触媒は、Fe系の触媒であり、NOxとしてNO2、NOおよびN2Oを想定した場合の反応式は、以下の(1)〜(3)の通りである。 The chemical synthesis facility (3) is supplied with NOx and electric power from the thermal power generation facility (1), supplied with hydrogen from the water splitting photocatalytic hydrogen production facility (2), and ammonia is synthesized using these as raw materials. The catalyst used for the reaction is an Fe-based catalyst, and the reaction formulas assuming NO 2 , NO, and N 2 O as NOx are as follows (1) to (3).
2NO + 5H2 → 2NH3 + 2H2O ・・・(1)
2NO2 + 7H2 → 2NH3 + 4H2O ・・・(2)
N2O + 4H2 → 2NH3 + H2O ・・・(3)
この反応における副生成物である水は、水分解光触媒水素製造設備(2)に再利用されてもよい。
2NO + 5H 2 → 2NH 3 + 2H 2 O (1)
2NO 2 + 7H 2 → 2NH 3 + 4H 2 O (2)
N 2 O + 4H 2 → 2NH 3 + H 2 O (3)
Water that is a by-product in this reaction may be reused in the water-splitting photocatalytic hydrogen production facility (2).
次に、本実施形態1の複合型火力発電システムを用いた場合について実施例1として具体的に説明する。 Next, the case where the combined thermal power generation system of the first embodiment is used will be specifically described as Example 1.
(実施例1)
火力発電設備(1)として、コンバインドサイクル火力発電設備を用いた。高位発熱量ベース(HHV基準)の発電効率は50%であり、火力発電燃料として液化天然ガス(LNG)、石油などを用いた。発電規模(出力)は250MWであった。
Example 1
A combined cycle thermal power generation facility was used as the thermal power generation facility (1). The power generation efficiency based on the higher heating value (HHV standard) was 50%, and liquefied natural gas (LNG), petroleum, etc. were used as the thermal power generation fuel. The power generation scale (output) was 250 MW.
水分解光触媒水素製造設備(2)について、太陽エネルギー変換効率は4%、設備(光触媒電極)面積は28,000m2(例えば5km×5.6km)、場内消費電力量:2×106kWh/day、水素製造規模(出力):350t/day−H2とした。 Regarding the water-splitting photocatalytic hydrogen production facility (2), the solar energy conversion efficiency is 4%, the facility (photocatalytic electrode) area is 28,000 m 2 (for example, 5 km × 5.6 km), and the power consumption in the field is 2 × 10 6 kWh / Day, hydrogen production scale (output): 350 t / day-H 2 .
日照時間を8hと仮定し、ある程度の日射強度(6kWh/m2/day)が得られるとすると、水分解光触媒水素製造設備(2)によって昼間3200tの淡水が水素(350t)と酸素に分解される。その際に場内で消費される電力量は反応を促進させるための補助的な電力量が主となり2,000MWh/dayと概算される。 Assuming that the sunshine duration is 8h and that a certain degree of solar radiation intensity (6 kWh / m 2 / day) is obtained, 3200 t of fresh water in the daytime is decomposed into hydrogen (350 t) and oxygen by the water splitting photocatalytic hydrogen production facility (2). The At that time, the amount of power consumed in the field is estimated to be 2,000 MWh / day mainly by an auxiliary power amount for promoting the reaction.
化学合成設備(3)をアンモニア合成設備とし、反応温度:500℃、反応圧力:20MPaであり、二重促進鉄を合成触媒に用いた。この合成触媒は、酸化鉄が主成分であり、酸化アルミニウム(シンタリング抑制)と酸化カリウムを含む。本設備におけるアンモニア製造能力は2,000t/day−NH3である。 The chemical synthesis facility (3) was an ammonia synthesis facility, the reaction temperature was 500 ° C., the reaction pressure was 20 MPa, and double promoted iron was used as the synthesis catalyst. This synthetic catalyst is composed mainly of iron oxide and contains aluminum oxide (sintering suppression) and potassium oxide. The ammonia production capacity in this facility is 2,000 t / day-NH 3 .
水分解光触媒水素製造設備(2)の水素製造量は、350t−H2/day(つまり175×106mol−H2/day)であるため、40×106〜70×106mol−NOx/dayの発生は、その全量をアンモニアに変換可能であると見込まれる。発生NOx量が生成水素量に比較して少ない場合は、深冷分離などにより別途精製された窒素を導入することで生成水素全量をアンモニアに変換可能である。 Since the hydrogen production amount of the water-splitting photocatalytic hydrogen production facility (2) is 350 t-H 2 / day (that is, 175 × 10 6 mol-H 2 / day), 40 × 10 6 to 70 × 10 6 mol-NOx. The generation of / day is expected to be able to convert the entire amount into ammonia. When the amount of generated NOx is smaller than the amount of generated hydrogen, the total amount of generated hydrogen can be converted to ammonia by introducing nitrogen that has been separately purified by cryogenic separation or the like.
貯蔵・輸送の観点で課題が多い水素をその場でアンモニアに変換することにより、それをキャリアとして貯蔵・輸送することが可能となる。アンモニアは直接あるいは分解して水素として輸送先のアプリケータで利用される。 By converting hydrogen, which has many problems from the viewpoint of storage and transportation, into ammonia on the spot, it can be stored and transported as a carrier. Ammonia is directly or decomposed and used as hydrogen in the destination applicator.
(実施の形態2)
図4は、実施の形態2の複合型火力発電システムを説明するフローシートである。
(Embodiment 2)
FIG. 4 is a flow sheet for explaining the combined thermal power generation system of the second embodiment.
本実施の形態2の複合型火力発電システムは、火力発電設備(1)と、水分解光触媒水素製造設備(2)と、化学合成設備(3)と、海水淡水化設備(4)とを有し、化学合成設備(3)は、火力発電設備(1)から排出されるNOxおよび水分解光触媒製造設備(2)で生成する水素を原料として利用してアンモニアを合成する。また、海水淡水化設備(4)は、火力発電設備(1)からの排出蒸気を熱源として利用し、海水淡水化設備(4)で製造された淡水が水分解光触媒製造設備(2)に供給される。
The combined thermal power generation system of
火力発電設備(1)、水分解光触媒水素製造設備(2)および化学合成設備(3)は、上記の実施の形態1のものと同様のものであるので、詳細な説明は省略する。 Since the thermal power generation facility (1), the water-splitting photocatalytic hydrogen production facility (2), and the chemical synthesis facility (3) are the same as those in the first embodiment, detailed description thereof is omitted.
海水淡水化設備(4)としては、火力発電設備(1)からの蒸気を熱源として用いて海水から淡水を製造することができるものであれば特に限定はなく、例えば、多段フラッシュ法、多重効用法などを用いた設備が挙げられる。また、海水淡水化設備(4)を駆動するための電力は、火力発電設備(1)から供給される。 The seawater desalination facility (4) is not particularly limited as long as it can produce freshwater from seawater using the steam from the thermal power generation facility (1) as a heat source. For example, the multistage flash method, multiple effects Equipment that uses the law. Electric power for driving the seawater desalination facility (4) is supplied from the thermal power generation facility (1).
海水淡水化設備(4)により製造された淡水は、水分解光触媒水素製造設備(2)に供給される。 Fresh water produced by the seawater desalination facility (4) is supplied to the water-splitting photocatalytic hydrogen production facility (2).
昼間に生成させられる淡水が水分解光触媒水素製造設備(2)に供給されて水素製造に利用される一方で、夜間に生成させられる淡水は飲料などの生活用水や工業用水として有効に利用される。 While fresh water generated in the daytime is supplied to the water-splitting photocatalytic hydrogen production facility (2) and used for hydrogen production, fresh water generated at night is effectively used as domestic water for drinks and industrial water. .
次に、本実施形態2の複合型火力発電システムを用いた場合について実施例2として具体的に説明する。 Next, the case where the combined thermal power generation system of the second embodiment is used will be specifically described as Example 2.
(実施例2)
火力発電設備(1)、水分解光触媒水素製造設備(2)および化学合成設備(3)については実施例1と同様であるので詳細な説明は省略する。
(Example 2)
Since the thermal power generation facility (1), the water-splitting photocatalytic hydrogen production facility (2) and the chemical synthesis facility (3) are the same as those in the first embodiment, detailed description thereof will be omitted.
海水淡水化設備(4)は、多段フラッシュ方式(MSF)の海水淡水化設備である。造水比:6〜10(約8)、場内消費電力量:4kWh/m3−生産淡水、淡水生産規模(出力):400t/hとした。 The seawater desalination facility (4) is a multistage flash (MSF) seawater desalination facility. Water production ratio: 6 to 10 (about 8), on-site power consumption: 4 kWh / m 3 -production fresh water, fresh water production scale (output): 400 t / h.
海水淡水化システムにおける必要蒸気量(導入時温度200℃)は、その造水比から40〜67t/hであり、火力発電設備(1)から導かれる量(450t/h)を考えると可能である。また、淡水(9,600t/day)を生産する際に場内で消費される電力量は、38.4MWh/dayと概算される。 The required amount of steam in the seawater desalination system (temperature at the time of introduction of 200 ° C.) is 40 to 67 t / h based on the water production ratio, which is possible considering the amount (450 t / h) derived from the thermal power generation facility (1). is there. In addition, the amount of power consumed in the field when producing fresh water (9,600 t / day) is estimated to be 38.4 MWh / day.
水分解光触媒水素製造設備(2)の水素製造量は、350t−H2/day(つまり175×106mol−H2/day)であるため、40×106〜70×106mol−NOx/dayの発生は、その全量をアンモニアに変換可能であると見込まれる。発生NOx量が生成水素量に比較して少ない場合は、深冷分離などにより別途精製された窒素を導入することで生成水素全量をアンモニアに変換可能である。 Since the hydrogen production amount of the water-splitting photocatalytic hydrogen production facility (2) is 350 t-H 2 / day (that is, 175 × 10 6 mol-H 2 / day), 40 × 10 6 to 70 × 10 6 mol-NOx. The generation of / day is expected to be able to convert the entire amount into ammonia. When the amount of generated NOx is small compared to the amount of generated hydrogen, the total amount of generated hydrogen can be converted to ammonia by introducing nitrogen purified separately by cryogenic separation or the like.
貯蔵・輸送の観点で課題が多い水素をその場でアンモニアに変換することにより、それをキャリアとして貯蔵・輸送することが可能となる。アンモニアは直接あるいは分解して水素として輸送先のアプリケータで利用される。 By converting hydrogen, which has many problems from the viewpoint of storage and transportation, into ammonia on the spot, it can be stored and transported as a carrier. Ammonia is directly or decomposed and used as hydrogen in the destination applicator.
1 火力発電設備
2 水分解光触媒水素製造設備
3 化学合成設備
1 Thermal
Claims (3)
The combined thermal power generation system according to claim 1, wherein water by-produced in the chemical synthesis facility is supplied to the water-splitting photocatalytic hydrogen production facility.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2011233079A JP5879091B2 (en) | 2011-10-24 | 2011-10-24 | Combined thermal power generation system |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2011233079A JP5879091B2 (en) | 2011-10-24 | 2011-10-24 | Combined thermal power generation system |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2013091577A JP2013091577A (en) | 2013-05-16 |
| JP5879091B2 true JP5879091B2 (en) | 2016-03-08 |
Family
ID=48615015
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011233079A Expired - Fee Related JP5879091B2 (en) | 2011-10-24 | 2011-10-24 | Combined thermal power generation system |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP5879091B2 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101767894B1 (en) | 2016-08-31 | 2017-08-14 | 한국에너지기술연구원 | Nitrogen circulation type system and method for treating nitrogen oxide |
| CN114352369B (en) * | 2021-11-30 | 2023-03-14 | 上海慕帆动力科技有限公司 | Gas turbine-steam turbine combined power generation system for producing hydrogen by decomposing ammonia and control method |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS54136599A (en) * | 1978-04-14 | 1979-10-23 | Mitsubishi Chem Ind Ltd | Production of ammonia |
| JPH11292531A (en) * | 1998-04-16 | 1999-10-26 | Nkk Sogo Sekkei Kk | Marine ammonia production equipment for exhaust gas denitrification |
| DE19922961C2 (en) * | 1999-05-19 | 2003-07-17 | Daimler Chrysler Ag | Emission control system with internal ammonia production for nitrogen oxide reduction |
| US7601308B2 (en) * | 2001-06-18 | 2009-10-13 | Coastal Hydrogen Energy, Inc. | Transition structures and catalytic reaction pathways for the production of hydrogen and oxygen |
| JP4117417B2 (en) * | 2002-03-15 | 2008-07-16 | 日立造船株式会社 | Ammonia production method and apparatus |
| JP4762555B2 (en) * | 2004-08-02 | 2011-08-31 | 日揮株式会社 | Power generation desalination method |
| US7371353B2 (en) * | 2005-08-31 | 2008-05-13 | Caterpillar Inc. | Exhaust purification with on-board ammonia production |
| JP2007075800A (en) * | 2005-09-16 | 2007-03-29 | Fuchino:Kk | Exhaust gas cleaning equipment and exhaust gas cleaning method used for exhaust gas cleaning equipment |
| US7767181B2 (en) * | 2006-06-30 | 2010-08-03 | Caterpillar Inc | System and method for ammonia production |
| CN101880046A (en) * | 2009-05-05 | 2010-11-10 | 中村德彦 | Compound equipment |
| WO2011116141A2 (en) * | 2010-03-18 | 2011-09-22 | Sun Hydrogen, Inc. | Clean steel production process using carbon-free renewable energy source |
-
2011
- 2011-10-24 JP JP2011233079A patent/JP5879091B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JP2013091577A (en) | 2013-05-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ES2963067T3 (en) | Ammonia cracking | |
| CN103298976B (en) | Method and energy carrier generating device for CO2-neutral balancing of current flow fluctuations due to power generation peaks and power generation troughs in an electrical network when generating electrical energy | |
| CN106285802B (en) | A kind of electricity-generating method and TRT | |
| JP5012559B2 (en) | Solar thermal energy storage and transfer method | |
| CN112601881B (en) | Hydrogen Energy Storage | |
| Chisalita et al. | Environmental evaluation of hydrogen production employing innovative chemical looping technologies–A Romanian case study | |
| US20080311022A1 (en) | Methods and apparatuses for ammonia production | |
| CA2767030A1 (en) | Recycling and reburning carbon dioxide in an energy efficient way | |
| AU2017381715B2 (en) | Removal of greenhouse gases and heavy metals from an emission stream | |
| EP3812033A1 (en) | Method and device for generating low-carbon-emission energy from fossils | |
| WO2009104813A1 (en) | Method of converting solar heat energy | |
| WO2022253256A1 (en) | Device and method for synthesizing methanol by using carbon dioxide and water | |
| JP5879091B2 (en) | Combined thermal power generation system | |
| CN217362587U (en) | Carbon-rich renewable combustion circulation system driven by new energy | |
| CN116036829A (en) | A system and working method for reducing carbon dioxide by using peak shaving and abandoning electricity to produce hydrogen and reduce carbon dioxide | |
| CN217362588U (en) | Alcohol-coal renewable combustion circulation system driven by new energy | |
| CN217354502U (en) | Carbon-based renewable combustion cycle system driven by new energy | |
| JP2013092065A (en) | Complex type thermal power system | |
| GB2456169A (en) | A method and associated apparatus for the production of hydrogen and/or electric energy | |
| CN206221012U (en) | A kind of TRT | |
| JP2007245017A (en) | Energy system | |
| Kumar et al. | An approach of CO 2 capture technology for mitigating global warming and climate change-an overview | |
| Zhu et al. | Assessment of Commercially Available Hydrogen Supply Chains for Gas-Fired Boilers | |
| Goswami et al. | Renewable Powered Multi-Stage Atmospheric CO 2 Reduction-A Key to Carbon Neutralization | |
| Chichilnisky et al. | Carbon negative power plants |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20140619 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20150227 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20150310 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20150508 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20151013 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20151210 |
|
| TRDD | Decision of grant or rejection written | ||
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20160105 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20160201 |
|
| R150 | Certificate of patent or registration of utility model |
Ref document number: 5879091 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
| LAPS | Cancellation because of no payment of annual fees |