JPH04121573A - Method of liquifying co2 gas - Google Patents
Method of liquifying co2 gasInfo
- Publication number
- JPH04121573A JPH04121573A JP2239001A JP23900190A JPH04121573A JP H04121573 A JPH04121573 A JP H04121573A JP 2239001 A JP2239001 A JP 2239001A JP 23900190 A JP23900190 A JP 23900190A JP H04121573 A JPH04121573 A JP H04121573A
- Authority
- JP
- Japan
- Prior art keywords
- refrigerant
- temperature
- gas
- intermediate refrigerant
- lng
- 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
Links
- 238000000034 method Methods 0.000 title claims abstract description 15
- 239000003507 refrigerant Substances 0.000 claims abstract description 39
- 238000009835 boiling Methods 0.000 claims abstract description 11
- 238000001704 evaporation Methods 0.000 claims abstract description 6
- 230000008020 evaporation Effects 0.000 claims abstract description 6
- 239000007788 liquid Substances 0.000 claims abstract description 6
- 239000004215 Carbon black (E152) Substances 0.000 claims abstract description 5
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 5
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 5
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 abstract description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 4
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 abstract description 3
- 239000000126 substance Substances 0.000 abstract description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 abstract 2
- 230000003247 decreasing effect Effects 0.000 abstract 1
- 238000005265 energy consumption Methods 0.000 abstract 1
- 239000001294 propane Substances 0.000 abstract 1
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 20
- 230000006835 compression Effects 0.000 description 4
- 238000007906 compression Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000001816 cooling Methods 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 238000009834 vaporization Methods 0.000 description 2
- 230000008016 vaporization Effects 0.000 description 2
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J1/00—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures
- F25J1/02—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures requiring the use of refrigeration, e.g. of helium or hydrogen ; Details and kind of the refrigeration system used; Integration with other units or processes; Controlling aspects of the process
- F25J1/0221—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures requiring the use of refrigeration, e.g. of helium or hydrogen ; Details and kind of the refrigeration system used; Integration with other units or processes; Controlling aspects of the process using the cold stored in an external cryogenic component in an open refrigeration loop
- F25J1/0222—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures requiring the use of refrigeration, e.g. of helium or hydrogen ; Details and kind of the refrigeration system used; Integration with other units or processes; Controlling aspects of the process using the cold stored in an external cryogenic component in an open refrigeration loop in combination with an intermediate heat exchange fluid between the cryogenic component and the fluid to be liquefied
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J1/00—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures
- F25J1/0002—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures characterised by the fluid to be liquefied
- F25J1/0027—Oxides of carbon, e.g. CO2
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J2210/00—Processes characterised by the type or other details of the feed stream
- F25J2210/62—Liquefied natural gas [LNG]; Natural gas liquids [NGL]; Liquefied petroleum gas [LPG]
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J2240/00—Processes or apparatus involving steps for expanding of process streams
- F25J2240/90—Hot gas waste turbine of an indirect heated gas for power generation
Landscapes
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Mechanical Engineering (AREA)
- Thermal Sciences (AREA)
- General Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Separation By Low-Temperature Treatments (AREA)
- Carbon And Carbon Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明はC02ガスの液化方法に関し、特に回収C02
ガスを液化する方法に関する。Detailed Description of the Invention [Field of Industrial Application] The present invention relates to a method for liquefying CO2 gas, and in particular to a method for liquefying CO2 gas.
This invention relates to a method for liquefying gas.
従来より、LNGの冷熱を利用し、中間冷媒であるハロ
ゲン化炭化水素(以下、フロンと略称する)を冷却し、
冷却したフロンによりCD2ガスを冷却液化する方法が
知られている。Conventionally, the cold energy of LNG is used to cool halogenated hydrocarbons (hereinafter abbreviated as fluorocarbons), which are intermediate refrigerants.
A method is known in which CD2 gas is cooled and liquefied using cooled Freon.
以下、第1図によって中間冷媒としてフロンを使用して
CO2ガスを液化する方法を説明する。Hereinafter, a method of liquefying CO2 gas using Freon as an intermediate refrigerant will be explained with reference to FIG.
第1図において、1.2は熱交換器、3はフロンの循環
ライン、4は同循環ポンプ、5はLNG (1)供給ラ
イン、6はLNG (g)排出ライン、7はCO2(g
)供給ライン、8はCD□(1)排出ラインである。In Figure 1, 1.2 is a heat exchanger, 3 is a fluorocarbon circulation line, 4 is a circulation pump, 5 is an LNG (1) supply line, 6 is an LNG (g) discharge line, and 7 is a CO2 (g)
) supply line, 8 is CD□(1) discharge line.
供給ライン5から熱交換器1に供給されたLNG <1
>の蒸発潜熱により循環ライン3を介して循環してくる
フロン(g)を冷却してフロン(g)をフロン<i>に
液化する。LNG(1)はLNG (g)に蒸発して排
出ライン6より系外に取出され、LNG (g)使用源
に供給される。LNG supplied from supply line 5 to heat exchanger 1 <1
The fluorocarbon (g) circulating through the circulation line 3 is cooled by the latent heat of vaporization of the fluorocarbon (g), and the fluorocarbon (g) is liquefied into fluorocarbon <i>. The LNG (1) is evaporated into LNG (g), taken out of the system through the discharge line 6, and supplied to the LNG (g) usage source.
フロン(1)は循環ポンプ4により熱交換器2に供給さ
れ、供給ライン7より供給されるC02(g)はフロン
(1)の蒸発潜熱によってCD。Freon (1) is supplied to the heat exchanger 2 by the circulation pump 4, and C02 (g) supplied from the supply line 7 is converted to CD by the latent heat of vaporization of the Freon (1).
(β)に冷却液化されて排出ライン8より系外に取出さ
れ、同時にフロン(i)はフロン、(g)となって循環
ライン3を介して上言己したように熱交換器1に循環さ
れる。(β) is cooled and liquefied and taken out of the system through the discharge line 8, and at the same time, the fluorocarbon (i) becomes fluorocarbon and (g) and is circulated through the circulation line 3 to the heat exchanger 1 as mentioned above. be done.
CD□ (g)を液化するに際しては、CD2は第3図
に示すような温度−圧力曲線を有するため、一般的に回
収されたCD2ガスは圧縮しなければならないが、これ
を圧縮するとCO2(g)は高温になるので、この高温
高圧CD□ (g)は空気又は水により冷却され、上記
第1図の系に供給される時には該COC02(は一般に
平均40℃程度の温度を有している。この40℃のCD
□(g)を通常の熱交換器2で中間冷媒(こ\ではフロ
ン)によって冷却する時には、温度の差(一般に、アプ
ローチ温度という)が必要であり、こ−では熱交換器2
に20℃の中間冷媒温度と液体CD□の温度差を設定し
た。When liquefying CD□ (g), since CD2 has a temperature-pressure curve as shown in Figure 3, the recovered CD2 gas generally has to be compressed, but when it is compressed, CO2 ( g) becomes high temperature, this high-temperature, high-pressure CD□ (g) is cooled with air or water, and when it is supplied to the system shown in Figure 1 above, the COC02 (generally has an average temperature of about 40°C). Yes, this 40℃ CD
□When (g) is cooled by an intermediate refrigerant (in this case, Freon) in a normal heat exchanger 2, a temperature difference (generally called approach temperature) is required.
The temperature difference between the intermediate refrigerant temperature and the liquid CD□ was set at 20°C.
CO2(g)をCD□ (Il)に液化するには供給ラ
イン7より供給されるCO2(g)の圧力を第3図に示
した温度−圧力曲線に見合った圧力にまで圧縮する必要
がある。In order to liquefy CO2 (g) into CD□ (Il), it is necessary to compress the pressure of CO2 (g) supplied from supply line 7 to a pressure commensurate with the temperature-pressure curve shown in Figure 3. .
この際、フロンの代表的なフロン22を中間冷媒とする
時には、フロン22の大気圧下の沸点は−40,8℃で
あるので、得られるC0C02(の温度は約−20,8
℃であり、CO2(g)を液化するためには供給co2
<g>の圧力を約20,4ataにしておかねばならな
い。このため、大気圧下のCOC02(を20. d
ataまで圧縮するエネルギーは相当なものとなる。At this time, when Freon 22, a typical type of fluorocarbon, is used as the intermediate refrigerant, the boiling point of Freon 22 under atmospheric pressure is -40.8°C, so the temperature of the obtained C0C02 is approximately -20.8°C.
℃, and in order to liquefy CO2 (g), the supply co2
The <g> pressure must be approximately 20.4 ata. For this reason, COC02 under atmospheric pressure (20. d
The energy required to compress it to ata is considerable.
更に、フロン22は規制対象外となっているもの\フロ
ンは地球大気層のオゾン層を破壊する原因物質として近
年その使用が禁止されようとする傾向にある。Furthermore, Freon-22 is not subject to regulation. In recent years, there has been a trend toward banning the use of Freon as it is a substance that causes the destruction of the ozone layer in the earth's atmosphere.
本発明は上記技術水準に鑑み、本発明はフロンに代わり
、フロンのような欠点がなく、しかもフロンを中間冷媒
としてCO2ガスを液化するよりもエネルギー消費を少
なくし得る中間冷媒を使用してCLガスを液化し得る方
法を提供し、併せて中間冷媒を冷却するのに使用して得
られるLNG (g)の有する圧力エネルギーを動力と
して回収し得る方法を提供しようとするものである。The present invention has been developed in view of the above-mentioned state of the art, and the present invention has been developed to replace fluorocarbons by using an intermediate refrigerant that does not have the disadvantages of fluorocarbons and can consume less energy than liquefying CO2 gas using fluorocarbons as an intermediate refrigerant. The object of the present invention is to provide a method that can liquefy gas, and also provide a method that can recover the pressure energy of LNG (g) obtained by cooling an intermediate refrigerant as power.
本発明は
(1)LNGの沸点においても凝固しないハロゲン元素
を含まない液体炭化水素系冷媒を中間冷媒とし、LNG
の蒸発潜熱により該中間冷媒を冷却液化し、該冷却液化
中間冷媒の蒸発潜熱によりC02ガスを凝固させること
なく液化させるC02ガスの液化方法。The present invention (1) uses a halogen-free liquid hydrocarbon refrigerant that does not solidify even at the boiling point of LNG as an intermediate refrigerant;
A method for liquefying CO2 gas by cooling and liquefying the intermediate refrigerant using the latent heat of evaporation of the cooling liquefied intermediate refrigerant, and liquefying the C02 gas without solidifying it using the latent heat of evaporation of the cooled and liquefied intermediate refrigerant.
(2)上記方法において、蒸発したLNGの高圧蒸気に
よりタービンを回転させて動力を回収するCD、ガスの
液化方法。(2) In the above method, a CD and gas liquefaction method in which power is recovered by rotating a turbine using high-pressure steam of evaporated LNG.
である。It is.
本発明において使用し得るハロゲン元素を含まない液体
炭化水素系冷媒としてはLNGの大気圧下の沸点(約−
161,5℃)においても凝固しない下表のものがあげ
られ、それぞれ単独又は混合して使用される。As a halogen-free liquid hydrocarbon refrigerant that can be used in the present invention, the boiling point of LNG under atmospheric pressure (approximately -
The following table shows that they do not solidify even at 161.5°C), and they can be used alone or in combination.
中間冷媒の具体例
なお、上記中間冷媒を単独又は混合して使用する時には
、その沸点を[:02 (g)が002(i)になるに
十分な温度であるが、凝固してC02(s)にならない
ように、中間冷媒の温度を高めておく必要がある。この
ような中間冷媒を単独又は混合し、中間冷媒循環ライン
に適宜の圧力に封入しておくことにより、CL (g
)と熱交換する熱交換器に供給する中間冷媒の温度を例
えば従来のフロン22の沸点(−40,8℃)よりも十
数℃も下げることができるので(勿論、それ以上低下さ
せることもできるが、co、の凝固を避けるためには、
これ以上沸点低下をもたらすことは許されない)それだ
け該熱交換器に供給するCLガスの加圧量を低めること
ができ、CD2ガス圧縮に要するエネルギー量を節約す
ることができる。Specific examples of intermediate refrigerants When using the above-mentioned intermediate refrigerants alone or in combination, the boiling point should be set to [:02 (g) at a temperature sufficient to become 002 (i), but solidify to C02 (s ), it is necessary to raise the temperature of the intermediate refrigerant. CL (g
) The temperature of the intermediate refrigerant supplied to the heat exchanger that exchanges heat with the refrigerant can be lowered by more than ten degrees Celsius than the boiling point (-40.8℃) of conventional Freon 22 (of course, it can be lowered even further). It is possible, but to avoid coagulation,
(No further reduction in boiling point is allowed) The amount of pressurized CL gas supplied to the heat exchanger can be reduced accordingly, and the amount of energy required for CD2 gas compression can be saved.
さらに、蒸発したLNG Cg)は高圧状態にあるので
、該ガスをタービンに供給して該タービンを回転させ動
力を回収することができるが、蒸発したLNG (g)
は余りにも低温なので、これを熱交換により例えば水で
加温し、常温程度のガス温度にまで昇温しでタービンに
供給するようにすることが好ましい。Furthermore, since the vaporized LNG (Cg) is under high pressure, the gas can be supplied to the turbine to rotate the turbine and recover power, but the vaporized LNG (Cg)
Since the temperature of the gas is too low, it is preferable to heat the gas by heat exchange with water, for example, to raise the gas temperature to about room temperature before supplying the gas to the turbine.
〔実施例1〕
以下、第11!!Iのフローに従って本発明の一実施例
として中間冷媒としてエタンを使用した場合と、従来の
中間冷媒であるフロン22を使用した場合とを下表に対
比して示し、本発明の効果を立証する。[Example 1] Below is the 11th! ! The effect of the present invention is demonstrated by comparing the case where ethane is used as an intermediate refrigerant as an example of the present invention according to the flow of I and the case where Freon 22, which is a conventional intermediate refrigerant, is used. .
上表の条件下において、本発明の実施例ではC02ガス
を1.03 ataから12.7 ataまで圧縮(2
段圧縮)すれば足りるので、[0□コンプレツサーの動
力は6210 KW)l/Hで十分であるのに対し、フ
ロン22を使用する従来例ではC02ガスを1.03
ataから20. d ataまで圧縮(2段圧縮)す
る必要があるので、7330 KIIIH/HのC02
コンプレツサの動力が必要である。Under the conditions shown in the table above, in the embodiment of the present invention, C02 gas is compressed from 1.03 ata to 12.7 ata (2
Stage compression) is sufficient, so [0□ compressor power is 6210 KW) l/h is sufficient, whereas in the conventional example using Freon 22, C02 gas is 1.03
20. from ata. Since it is necessary to compress (two-stage compression) to d data, C02 of 7330 KIIIH/H
Compressor power is required.
この結果、本発明実施例では従来法に比し大幅な動力の
節減が達成される。As a result, the embodiment of the present invention achieves a significant power saving compared to the conventional method.
上記実施例では中間冷媒としてエタンを使用する場合の
例を示したが、本発明はこれに限定されるものではなく
、第1表に示した他の中間冷媒を単独又は混合し、適宜
中間冷媒循環ライン中の封入圧力を設定することにより
、それ相当の動力消費量の節減が可能である。Although the above embodiment shows an example in which ethane is used as the intermediate refrigerant, the present invention is not limited to this, and other intermediate refrigerants shown in Table 1 may be used alone or in a mixture, and the intermediate refrigerant may be used as appropriate. By setting the confinement pressure in the circulation line, corresponding savings in power consumption are possible.
〔実施例2〕
第2図に示すフローに従って、本発明のLNGガスより
動力回収の実施例を示し、本発明の効果を立証する。第
2図において、符号1〜8は第1図と同じであるので説
明は省略する。第2図の加わった符号9は熱交換器、1
0は膨張タービンである。[Example 2] According to the flow shown in FIG. 2, an example of power recovery from LNG gas of the present invention will be shown to prove the effects of the present invention. In FIG. 2, numerals 1 to 8 are the same as in FIG. 1, so their explanation will be omitted. The added numeral 9 in FIG. 2 is a heat exchanger, 1
0 is an expansion turbine.
第2図において、熱交換器1より排出ライン6を介して
排出される低温のLNG (g)は熱交換器9により、
例えば水などと熱交換された後、膨張タービン10に供
給されて動力を回収される。In FIG. 2, low-temperature LNG (g) discharged from the heat exchanger 1 through the discharge line 6 is transferred to the heat exchanger 9.
After exchanging heat with water, for example, it is supplied to the expansion turbine 10 and power is recovered.
実施例1に対比して示した条件で模作し、排出ライン6
より排出される低温のLNG (g)を熱交換器9で2
0℃に昇温し、膨張タービン10に入口圧力10ata
で供給し、出口圧力4ataで取出した時、本発明の実
施例の条件では回収動力は3140にWH/IIである
。A replica was made under the conditions shown in comparison with Example 1, and the discharge line 6
The low-temperature LNG (g) discharged from the
The temperature is raised to 0°C, and the inlet pressure to the expansion turbine 10 is 10ata.
When supplied at a pressure of 4ata and taken out at an outlet pressure of 4ata, the recovery power is 3140 WH/II under the conditions of the embodiment of the present invention.
該実施例2によっても本発明方法はCD、ガスの液化に
際し、動力回収が行なえ、工業的に有利なことが判る。It can be seen from Example 2 that the method of the present invention can recover power during liquefaction of CD and gas, and is industrially advantageous.
本発明によればCD、ガスの液化に際し、C02ガス圧
縮による動力エネルギーが従来法に比し大幅に節減でき
る効果を奏すると共に、動力回収が行なえ、その工業的
価値は極めて顕著である。According to the present invention, when liquefying CD gas, the power energy due to CO2 gas compression can be significantly reduced compared to the conventional method, and the power can be recovered, and its industrial value is extremely significant.
第1図は従来技術および本発明の実施例1の説明図、第
2図は本発明の実施例2の説明図、第3図はC02ガス
の液化曲線の温度−圧力関係図表である。FIG. 1 is an explanatory diagram of the prior art and Embodiment 1 of the present invention, FIG. 2 is an explanatory diagram of Embodiment 2 of the present invention, and FIG. 3 is a temperature-pressure relationship chart of the liquefaction curve of C02 gas.
Claims (2)
を含まない液体炭化水素系冷媒を中間冷媒とし、LNG
の蒸発潜熱により該中間冷媒蒸気を冷却液化し、該冷却
液化中間冷媒の蒸発潜熱によりCO_2ガスを凝固させ
ることなく液化させることを特徴とするCO_2ガスの
液化方法。(1) A halogen-free liquid hydrocarbon refrigerant that does not solidify even at the boiling point of LNG is used as an intermediate refrigerant, and LNG
A method for liquefying CO_2 gas, characterized in that the intermediate refrigerant vapor is cooled and liquefied by the latent heat of evaporation of the cooled liquefied intermediate refrigerant, and the CO_2 gas is liquefied without being solidified by the latent heat of evaporation of the cooled and liquefied intermediate refrigerant.
LNG蒸気によりタービンを回転させて動力を回収する
ことを特徴とするCO_2ガスの液化方法。(2) A method for liquefying CO_2 gas according to claim (1), characterized in that power is recovered by rotating a turbine using evaporated high-pressure LNG steam.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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JP2239001A JP2566337B2 (en) | 1990-09-11 | 1990-09-11 | CO ▲ 2 ▼ Gas liquefaction method |
Applications Claiming Priority (1)
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JP2239001A JP2566337B2 (en) | 1990-09-11 | 1990-09-11 | CO ▲ 2 ▼ Gas liquefaction method |
Publications (2)
Publication Number | Publication Date |
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JPH04121573A true JPH04121573A (en) | 1992-04-22 |
JP2566337B2 JP2566337B2 (en) | 1996-12-25 |
Family
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JP2239001A Expired - Lifetime JP2566337B2 (en) | 1990-09-11 | 1990-09-11 | CO ▲ 2 ▼ Gas liquefaction method |
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5932127B2 (en) * | 2013-02-25 | 2016-06-08 | 三菱重工コンプレッサ株式会社 | Carbon dioxide liquefaction equipment |
JP2020051674A (en) * | 2018-09-26 | 2020-04-02 | 関西電力株式会社 | Heat exchange equipment, power generation facility and heat exchange method |
CN113465201A (en) * | 2021-08-05 | 2021-10-01 | 西安热工研究院有限公司 | Cold-heat combined supply and energy storage system and method based on carbon dioxide compression coupling molten salt heat storage |
FR3128011A1 (en) * | 2022-05-20 | 2023-04-14 | L'air Liquide, Societe Anonyme Pour L'etude Et L'exploitation Des Procedes Georges Claude | Method and apparatus for cooling a CO2-rich flow |
EP4191177A1 (en) * | 2021-12-01 | 2023-06-07 | Nederlandse Organisatie Voor Toegepast- Natuurwetenschappelijk Onderzoek Tno | Lng exergy optimization for sbcc |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0448185A (en) * | 1990-06-14 | 1992-02-18 | Central Res Inst Of Electric Power Ind | Recovering method of carbon dioxide discharged out of lng burning thermal power station |
-
1990
- 1990-09-11 JP JP2239001A patent/JP2566337B2/en not_active Expired - Lifetime
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0448185A (en) * | 1990-06-14 | 1992-02-18 | Central Res Inst Of Electric Power Ind | Recovering method of carbon dioxide discharged out of lng burning thermal power station |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5932127B2 (en) * | 2013-02-25 | 2016-06-08 | 三菱重工コンプレッサ株式会社 | Carbon dioxide liquefaction equipment |
JP2020051674A (en) * | 2018-09-26 | 2020-04-02 | 関西電力株式会社 | Heat exchange equipment, power generation facility and heat exchange method |
CN113465201A (en) * | 2021-08-05 | 2021-10-01 | 西安热工研究院有限公司 | Cold-heat combined supply and energy storage system and method based on carbon dioxide compression coupling molten salt heat storage |
CN113465201B (en) * | 2021-08-05 | 2022-09-27 | 西安热工研究院有限公司 | Cold-heat combined supply and energy storage system and method based on carbon dioxide coupling molten salt heat storage |
EP4191177A1 (en) * | 2021-12-01 | 2023-06-07 | Nederlandse Organisatie Voor Toegepast- Natuurwetenschappelijk Onderzoek Tno | Lng exergy optimization for sbcc |
WO2023101550A1 (en) * | 2021-12-01 | 2023-06-08 | Nederlandse Organisatie Voor Toegepast-Natuurwetenschappelijk Onderzoek Tno | Lng exergy optimization for sbcc |
FR3128011A1 (en) * | 2022-05-20 | 2023-04-14 | L'air Liquide, Societe Anonyme Pour L'etude Et L'exploitation Des Procedes Georges Claude | Method and apparatus for cooling a CO2-rich flow |
EP4279848A1 (en) | 2022-05-20 | 2023-11-22 | L'air Liquide, Societe Anonyme Pour L'etude Et L'exploitation Des Procedes Georges Claude | Method and apparatus for cooling a co2-rich flow |
Also Published As
Publication number | Publication date |
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JP2566337B2 (en) | 1996-12-25 |
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