Gas capture and storage system and method

By introducing a gas conveying unit into the ship's carbon capture system, the desorption gas is used to reduce the partial pressure of carbon dioxide, the problem of high desorption energy consumption in the prior art is solved, and the system operation cost and higher carbon capture efficiency are achieved.

WO2025066493A1PCT designated stage expired Publication Date: 2025-04-03NO 711 RES INST CHINA SHIPPING HEAVY IND GRP

Patent Information

Application Number
PCT/CN2024/107327
Authority / Receiving Office
WO · WO
Patent Type
Applications
Current Assignee / Owner
Priority Date
2023-09-28
Filing Date
2024-07-24
Publication Date
2025-04-03

AI Technical Summary

Technical Problem

The existing ship carbon capture and storage technology has the problem of high desorption energy consumption, which is difficult to meet the application needs of actual ships.

Method used

A gas capture and storage system is provided, including an absorption unit, a desorption unit and a gas conveying unit. By desorbing the gas, the partial pressure of carbon dioxide in the desorption system is reduced, the carbon dioxide desorption reaction occurs, and the regeneration energy consumption of the desorption system is reduced.

Benefits of technology

It reduces the operating costs of the system and improves the application efficiency of carbon capture technology in the field of marine carbon emission reduction.

✦ Generated by Eureka AI based on patent content.

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Abstract

The present application discloses a gas capture and storage system and a method. The gas capture and storage system of the present application comprises: an absorption unit, a desorption unit, and a gas transfer unit. A carbon-containing flue gas is fed into the absorption unit, and comes into contact with an absorption liquid in the absorption unit to form a first solution, and the first solution is fed into the desorption unit. A desorption gas is fed into the desorption unit by means of the gas transfer unit, and comes into contact with the first solution to complete desorption of at least part of carbon dioxide to form a second solution, and the second solution is fed into the absorption unit.
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Description

Gas capture and storage system and method

[0001] This application claims priority to the Chinese patent application filed with the China Patent Office on September 28, 2023, with application number 202311284358.7 and invention name “A Gas Capture and Storage System and Method”, the entire contents of which are incorporated by reference into this application. Technical Field

[0002] The present application relates to, but is not limited to, the field of ship exhaust gas purification. Background Art

[0003] Ship carbon capture and storage post-processing technology has become an important technical route for ship emissions due to its advantages such as large emission reduction capabilities, good matching with ship operating conditions, and economy. Technical Solutions

[0004] In a first aspect, an embodiment of the present application provides a gas capture and storage system, comprising:

[0005] an absorption unit having a first inlet and a first outlet, wherein carbonaceous flue gas is fed into the absorption unit through the first inlet, wherein the carbonaceous flue gas contains carbon dioxide, and the carbonaceous flue gas contacts an absorption liquid in the absorption unit to form a first solution, which is discharged through the first outlet;

[0006] a desorption unit having a second inlet, wherein the first solution delivered from the first outlet is delivered to the desorption unit through the second inlet;

[0007] A gas transfer unit is used to feed desorption gas into the desorption unit, wherein the desorption gas contacts the first solution to complete the desorption of at least part of the carbon dioxide to form a second solution, and the second solution is fed from the desorption unit to the absorption unit.

[0008] Optionally, a circulation unit is further included, wherein the circulation unit includes a first circulation pump, the inlet of the first circulation pump is connected to the first outlet, and the outlet of the first circulation pump is connected to the second inlet.

[0009] Optionally, the circulation unit includes a second circulation pump, the absorption unit has a third inlet, the desorption unit has a second outlet, the inlet of the second circulation pump is connected to the second outlet, and the outlet of the second circulation pump is connected to the third inlet.

[0010] Optionally, the circulation unit includes a heat exchanger, which is connected to the outlet of the first circulation pump and the outlet of the second circulation pump respectively.

[0011] Optionally, the heat exchanger has a first heat exchange outlet, which is communicated with the second inlet; the heat exchanger has a second heat exchange outlet, which is communicated with the third inlet.

[0012] Optionally, the circulation unit includes a first heater, which is arranged between the first heat exchange outlet and the second inlet.

[0013] Optionally, the circulation unit includes a cooler, which is arranged between the second heat exchange outlet and the third inlet.

[0014] Optionally, the gas transfer unit includes a membrane separator, the desorption unit has a third outlet, and the inlet of the membrane separator is connected to the third outlet.

[0015] Optionally, the gas transfer unit includes a condenser, which is arranged between the membrane separator and the third outlet.

[0016] Optionally, the gas transfer unit includes a second heater, the desorption unit has a fourth inlet, and the second heater is arranged between the membrane separator and the fourth inlet.

[0017] Optionally, the gas delivery unit has a fifth inlet, and the fifth inlet is used to introduce desorption gas.

[0018] In a second aspect, the present application also provides a gas capture method, comprising:

[0019] The carbon-containing flue gas is fed into an absorption unit, wherein the absorption unit contains an absorption liquid. The carbon-containing flue gas includes carbon dioxide. After the absorption liquid contacts the carbon-containing flue gas, a first solution is formed.

[0020] The first solution is fed into a desorption unit, and a gas delivery unit feeds a desorption gas into the desorption unit for desorbing carbon dioxide in the first solution;

[0021] The first solution after desorption forms a second solution, and the second solution is sent from the desorption unit to the absorption unit.

[0022] Optionally, the absorption unit has a first air pressure, and the pressure range of the first air pressure is 0.8 to 1.2 bar.

[0023] Optionally, the absorption unit has a first temperature, and the first temperature ranges from 30 to 40°C.

[0024] Optionally, the desorption unit has a second air pressure, and the pressure range of the second air pressure is 0.8 to 1.2 bar.

[0025] Optionally, the desorption unit has a second temperature, and the second temperature ranges from 80 to 90°C. BRIEF DESCRIPTION OF THE DRAWINGS

[0026] In order to more clearly illustrate the technical solutions in the embodiments of the present application, the following briefly introduces the drawings required for use in the description of the embodiments. Obviously, the drawings described below are only some embodiments of the present application. For those skilled in the art, other drawings can be obtained based on these drawings without creative work.

[0027] Figure 1 is a diagram showing the principle of gas stripping and desorption based on the double membrane theory;

[0028] FIG2 is a schematic structural diagram of a gas capture and storage system according to an embodiment of the present application;

[0029] FIG3 is a flow chart of the gas capture method in an embodiment of the present application. DETAILED DESCRIPTION

[0030] The following will provide a clear and complete description of the technical solutions in the embodiments of the present application, in conjunction with the embodiments and accompanying drawings. It should be noted that the described embodiments are only a portion of the embodiments of the present application, and are not intended to be exhaustive. All other embodiments derived by persons skilled in the art based on the embodiments of the present application without inventive effort are intended to fall within the scope of protection of the present application. Furthermore, in the description of the present application, the term "including" means "including but not limited to." The terms "first," "second," and "third," etc., are used merely as designations and do not impose numerical requirements or establish a sequence. Various embodiments of the present application may be presented in the form of a range. It should be understood that describing in a range format is merely for convenience and brevity and should not be construed as a rigid limitation on the scope of the present application. Therefore, the range description should be considered to specifically disclose all possible subranges and individual numerical values ​​within the range. For example, a range description of 1 to 6 should be considered to specifically disclose subranges, such as 1 to 3, 1 to 4, 1 to 5, 2 to 4, 2 to 6, 3 to 6, etc., as well as individual numerical values ​​within the range, such as 1, 2, 3, 4, 5, and 6, regardless of the range. Additionally, whenever a numerical range is indicated herein, it is meant to include any cited numeral (fractional or integral) within the indicated range.

[0031] The basic principle of gas stripping desorption of CO2 is based on the double-membrane theory, as shown in Figure 1. The double-membrane theory believes that there is a phase interface between the gas and liquid phases in contact with each other, with a gas film and a liquid film on both sides. During the desorption process, the concentration gradient between the gas film and the liquid film is the driving force for the mass transfer of CO2 between the gas phase and the liquid phase. Due to the different CO2 partial pressures in the gas and liquid phases, under the impetus of the pressure difference, CO2 reaches the liquid film by molecular diffusion, and then enters the gas film through the phase interface, thereby desorbing CO2 from the absorption rich liquid. Therefore, nitrogen or solvent vapor without solute is used as a carrier gas to blow CO2 out of the absorption liquid, reduce the gas phase CO2 partial pressure, thereby increasing the mass transfer driving force of the desorption process, and thus allowing CO2 to be continuously desorbed from the absorption rich liquid. The advantage of gas stripping for CO2 desorption is that it requires less energy, promotes the CO2 desorption reaction rate, and reduces the CO2 desorption reaction temperature, thereby reducing the energy consumption of the CO2 desorption process and lowering the system operating costs. Moreover, the greater the amount of gas introduced, the greater the amount of CO2 desorbed. However, due to the limitations of the ship's operating environment, the captured and desorbed CO2 needs to be stored in onboard tanks and subsequently transported for utilization. This process still has high requirements for the purity of CO2. Ship carbon capture and storage post-processing technology has become an important technical route for ship emissions due to its advantages such as strong emission reduction, good compatibility with ship operating conditions, and economy. Although this technology can achieve large-scale carbon emission reduction, it has the problem of high system desorption energy consumption, which makes it difficult to meet the application needs of actual ships.

[0032] In order to solve the problems existing in the prior art, the present application provides a gas capture and storage system, as shown in Figure 2, including: an absorption unit 100, the absorption unit 100 has a first inlet 101 and a first outlet 102, carbon-containing flue gas is fed into the absorption unit 100 from the first inlet 101, the carbon-containing flue gas contains carbon dioxide, the carbon-containing flue gas contacts with the absorption liquid in the absorption unit 100 to form a first solution, and the first solution is fed out from the first outlet 102; a desorption unit 200, the desorption unit 200 has a second inlet 201, the first solution fed out of the first outlet 102 is fed into the desorption unit 200 from the second inlet 201; a gas transfer unit 300, the gas transfer unit 300 is used to feed desorption gas into the desorption unit 200, the desorption gas contacts with the first solution to complete the desorption of at least part of the carbon dioxide to form a second solution, and the second solution is fed from the desorption unit 200 into the absorption unit 100. The gas capture and storage system of the present application utilizes desorption gas to reduce the partial pressure of carbon dioxide in the desorption system while ensuring the complete functionality of the ship power carbon capture system, thereby promoting the desorption reaction of carbon dioxide, reducing the regeneration energy consumption of the desorption system, and reducing the operating costs of the system, which can further promote the application of carbon capture technology in the field of ship carbon emission reduction.

[0033] In some embodiments, the gas capture storage system further includes a circulation unit 400 , which includes a first circulation pump 401 . The inlet of the first circulation pump 401 is connected to the first outlet 102 and the second inlet 201 .

[0034] In some embodiments, the main structure of the absorption unit 100 is an absorption tower, which has a first inlet 101 for feeding carbon-containing flue gas. In some embodiments, the first inlet 101 is located below the absorption tower, and the carbon-containing flue gas is fed into the bottom of the absorption tower from the first inlet 101, and the carbon-containing flue gas flows from bottom to top in the absorption tower.

[0035] In some implementations, the absorption unit 100 has a third inlet 103. In some embodiments, the third inlet is located above the absorption tower, and the absorption liquid is sprayed from the absorption tower from top to bottom. The carbon-containing flue gas enters from the bottom of the absorption tower and flows upward to complete the adsorption of the carbon-containing flue gas by the absorption liquid, wherein the carbon dioxide in the carbon-containing flue gas is adsorbed by the absorption liquid to form a first solution (rich liquid).

[0036] In some implementations, fillers may be arranged in the absorption tower to increase the contact area between the absorption liquid and the carbonaceous flue gas and the adsorption efficiency. In some specific embodiments, the fillers may be selected from one or more of corrugated plates, ceramic fillers, and metal fillers. The fillers may be bulk or structured packing.

[0037] In some embodiments, the form, size, model and specification of the packing can be selected based on parameters such as actual CO2 removal efficiency, pressure drop requirements in the absorption tower, liquid flooding rate requirements and operating conditions.

[0038] In some embodiments, the absorption liquid includes an organic amine solution, and single or mixed organic amine solutions such as MEA (ethanolamine), MDEA (2-methyl-diethylaminoethanolamine), and DEA (diethanolamine) can be used.

[0039] In some embodiments, after the carbon-containing flue gas is adsorbed by the absorption liquid, the clean flue gas is discharged from the top of the absorption tower.

[0040] In some embodiments, the main structure of the desorption unit 200 is a desorption tower 210, and the first solution (rich liquid, absorption liquid that has absorbed CO2) in the desorption tower 210 is sent into the desorption tower 210 under the action of a pump group.

[0041] In some embodiments, a second inlet 201 is provided on the desorption tower 210, and the first solution is fed into the desorption tower from the second inlet 201. In some embodiments, the second inlet 201 is located above the desorption tower 210, and the first solution is fed into the desorption tower 210 from the top of the desorption tower 210.

[0042] In some embodiments, a desorption gas is simultaneously introduced into the desorption tower 210. The desorption gas may be solute-free nitrogen or solvent vapor. In some embodiments, the desorption tower 210 has a fourth inlet 204 through which the desorption gas is introduced. In some specific embodiments, the fourth inlet 204 is disposed within the desorption tower 210. The rich solution is desorbed within the desorption tower 210, releasing CO2 and forming a second solution (lean solution).

[0043] In some embodiments, the desorption tower 210 has a second outlet 202 . In some embodiments, the second outlet 202 is located at the bottom of the desorption tower 210 , and the second solution is fed into the absorption tower 110 through the second outlet 202 .

[0044] In some embodiments, the desorption tower 210 has a third outlet 203. In some embodiments, the third outlet 203 is located at the top of the desorption tower 210. The third outlet 203 is used to deliver the product gas in the desorption tower 210. In some specific application examples, the product gas at the third outlet 203 at the top of the desorption tower 210 includes CO2, N2, and a small amount of water vapor, and is delivered to the gas delivery unit 300.

[0045] In some embodiments, gas transfer unit 300 includes a membrane separator 301, the inlet of which is connected to third outlet 203. In some embodiments, membrane separator 301 is a nitrogen membrane separator, which separates nitrogen from carbon dioxide. The separated carbon dioxide is a high-purity gas and is sent to a storage tank for storage. The nitrogen separated by membrane separator 301 is then recirculated to desorption tower 210. In some embodiments, membrane separator 301 is equipped with a self-pressurizing device to increase the pressure of the product gas. After passing through the membrane separator, if the pressure meets the requirements of the onboard liquefaction module, the traditional compression module can be eliminated and the product gas at the required pressure can be directly liquefied and stored.

[0046] In order to purify the product gas, the gas transfer unit 300 also includes a condenser 302, which is arranged between the membrane separator 301 and the third outlet 203. The condenser 302 is used to separate the water vapor in the product gas, and the separated condensed water vapor is sent to the desorption tower 210 for circulation to supplement the water vapor evaporation loss in the desorption tower 210.

[0047] In some embodiments, the gas transfer unit 300 includes a second heater 303, the desorption unit 200 has a fourth inlet 204, and the second heater 303 is arranged between the membrane separator 301 and the fourth inlet 204, and is used to heat the desorption gas sent into the desorption tower 210 to maintain the temperature inside the desorption tower 210. In some specific embodiments, the second heater 303 is an electric heater. In some specific embodiments, the temperature of the desorption gas heated by the second heater 303 is between 85 and 95°C, such as 90°C.

[0048] In some embodiments, the gas transfer unit 300 has a fifth inlet 304, which is used to feed desorption gas. In some specific embodiments, the fifth inlet 304 is located between the second heater 303 and the membrane separator 301. For example, nitrogen can be fed into the fifth inlet 304, and enters the second heater 303 together with the nitrogen sent from the membrane separator 301 for heating, and then is sent into the desorption tower 210 to supplement or adjust the amount of desorption gas fed into the desorption tower 210.

[0049] In some embodiments, the capture and storage system of the present application further includes a circulation unit 400 , which includes a first circulation pump 401 . The inlet of the first circulation pump 401 is connected to the first outlet 102 and the second inlet 201 . In some embodiments, the first circulation pump 401 is a rich liquid circulation pump.

[0050] The circulation unit 400 includes a second circulation pump 402, the absorption unit 100 has a third inlet 103, the desorption unit 200 has a second outlet 202, the inlet of the second circulation pump 402 is connected to the second outlet 202, and the outlet of the second circulation pump 402 is connected to the third inlet 103. In some embodiments, the second circulation pump 402 is a lean liquid circulation pump.

[0051] In order to adjust the temperature of the lean / rich liquid sent into the absorption tower 110 and the desorption tower 210, the circulation unit 400 includes a heat exchanger 403, which is connected to the outlet of the first circulation pump 401 and the outlet of the second circulation pump 402 respectively. The heat exchanger 403 has a first heat exchange outlet 4031, which is connected to the second inlet 201; the heat exchanger 403 has a second heat exchange outlet 4032, which is connected to the third inlet 103.

[0052] In some embodiments, the temperature range of the first solution sent from the outlet of the first circulation pump 401 to the heat exchanger 403 is 30-40°C. After heat exchange in the heat exchanger 403, the temperature of the rich liquid sent from the first heat exchange outlet 4031 of the heat exchanger 403 is about 75-85°C, such as 80°C.

[0053] In some embodiments, the temperature of the second solution sent from the outlet of the second circulation pump 402 to the heat exchanger 403 is in the range of 85 to 95°C, such as 90°C. After heat exchange in the heat exchanger 403, the temperature of the lean liquid sent from the second heat exchange outlet 4032 of the heat exchanger 403 is about 45 to 55°C, such as 50°C.

[0054] In some embodiments, the circulation unit 400 includes a first heater 404 disposed between the first heat exchange outlet 4031 and the second inlet 201. The first heater 404 is used to heat the first solution sent from the heat exchanger 403 to a desired temperature, such as from 80°C to 90°C.

[0055] In some embodiments, the circulation unit 400 includes a cooler 405, which is arranged between the second heat exchange outlet 4032 and the third inlet 103. The cooler 405 is used to reduce the temperature of the second solution entering the absorption tower 110, such as reducing the temperature of the second solution from 50°C to 40°C.

[0056] As shown in FIG3 , a gas capture method using the gas capture storage system shown in FIG2 includes:

[0057] The carbon-containing flue gas is fed into the absorption unit 100, which contains an absorption liquid. The carbon-containing flue gas includes carbon dioxide. After the absorption liquid contacts the carbon-containing flue gas, a first solution is formed; the first solution is fed into the desorption unit 200, and the gas transfer unit 300 feeds desorption gas into the desorption unit 200 to desorb the carbon dioxide in the first solution; the first solution after desorption forms a second solution, and the second solution is fed from the desorption unit 200 into the absorption unit 100.

[0058] In some specific application examples, high-temperature ship exhaust containing CO2 first flows through absorption tower 110, where the exhaust and the absorbent undergo countercurrent convection mass transfer. The clean exhaust then exits through the top of absorption tower 110. The rich liquid, heated by the pump assembly, is then passed through heat exchanger 403 and enters desorption tower 210 from the top. Within desorption tower 210, the rich liquid enters from the top, while nitrogen, heated by first heater 404, enters from the bottom. The hot nitrogen desorbs the rich liquid, releasing CO2. The product gas (CO2 + N2 + a small amount of water vapor) exits the top of the desorption tower and passes through condenser 302 and membrane separator 301. The purified, high-purity CO2 gas is then discharged from the system for further storage. The separated nitrogen passes through membrane separator 301 and first heater 404 and then enters the bottom of desorption tower 210, continuing the next cycle.

[0059] In some specific embodiments, the absorption liquid is an organic amine solution. This application uses an organic amine solution to chemically absorb and desorb CO2 from carbon-containing flue gas. The desorption gas is nitrogen, and nitrogen stripping desorption is performed to reduce the CO2 partial pressure in the desorption tower 210 environment, thereby promoting the desorption reaction. The forward reaction (absorption) occurs at room temperature (30-40°C) and atmospheric pressure, while the reverse reaction (desorption) occurs at a lower temperature (80-90°C) and atmospheric pressure.

[0060] In a specific application example, the absorption tower 110 has a first air pressure, and the pressure range of the first air pressure is 0.8 to 1.2 bar, such as the first air pressure is 1 bar. The optimal air pressure of the absorption tower 110 of the present application is 1 bar, and the entire system does not need to apply any pressure, which reduces the pressure on components such as the circulation pump in the circulation unit 400. In addition, nitrogen gas is used to reduce the CO2 gas partial pressure in the desorption tower 210, promote the CO2 desorption reaction, reduce the system regeneration energy consumption, and cut the system operating cost. In a specific application example, the absorption tower 110 has a first temperature, and the first temperature range is 30 to 40°C.

[0061] In a specific application example, the desorption tower 210 has a second pressure, and the second pressure ranges from 0.8 to 1.2 bar, such as 1 bar. The optimal pressure for the desorption tower 210 of the present application is 1 bar, and the entire system does not require any pressure, which reduces the pressure on components such as the circulation pump in the circulation unit 400 and the amount of pumps required, thereby reducing construction difficulty. In a specific application example, the desorption tower 210 has a second temperature, and the second temperature ranges from 80°C to 90°C.

[0062] The present application adopts nitrogen stripping to desorb CO2, which eliminates the need to heat the absorption liquid to the desorption temperature of 110-120°C, reduces the energy consumption demand on the ship side, and ensures the functional integrity of the system.

[0063] In some embodiments, carbon dioxide is captured by:

[0064] The carbon-containing flue gas is fed into the absorption unit 100. The absorption unit 100 contains an absorption liquid. The carbon-containing flue gas includes carbon dioxide. After the absorption liquid and the carbon-containing flue gas come into contact, a first solution is formed. The absorption liquid in the absorption tower 110 is an organic amine solution. The temperature in the absorption tower is 40°C and the pressure in the absorption tower 110 is 1 bar.

[0065] After the first solution is heat exchanged in the heat exchanger 403, it is sent to the desorption unit 200. The temperature of the first solution after heat exchange in the heat exchanger 403 rises from 40°C to 80°C. When the temperature in the desorption tower 210 is maintained at 80°C, the first heater 404 does not need to be heated. When the temperature in the desorption tower 210 is maintained at 90°C, the rich solution is heated to 90°C by the first heater 404 and sent to the desorption tower 210.

[0066] The gas transfer unit 300 feeds desorption gas into the desorption unit 200. The desorption gas is nitrogen. The nitrogen is heated to 90°C by the second heater 303 and fed into the desorption tower 210 from bottom to top to desorb carbon dioxide in the first solution. The temperature of the desorption tower 210 is maintained at 80-90°C and the pressure is 1 bar. In this embodiment, the temperature of the desorption tower 210 is maintained at 90°C.

[0067] After desorption, the first solution forms a second solution. After the second solution passes through the heat exchanger 403 for heat exchange, the temperature of the second solution drops from 90°C to 50°C. Subsequently, the second solution is cooled to 40°C by a cooler arranged between the heat exchanger 403 and the third inlet 103 of the absorption tower 110 and is sent to the absorption tower 110.

[0068] The product gas sent out from the third outlet 203 of the desorption tower 210 is cooled to 30° C. by the condenser 302 and sent to the nitrogen membrane separator. The carbon dioxide separated by the nitrogen membrane separator is sent to the next process, and the separated nitrogen enters the cycle again.

[0069] Please refer to Table 1, which compares the energy consumption of carbon dioxide desorption in Table 1 with the energy consumption of the gas stripping desorption method of the present application: the setting parameters of the absorption tower are the same, and the difference between carbon dioxide desorption and the present application is that no gas transfer unit is set, the temperature range in the desorption tower in the carbon dioxide desorption method is 110-120°C, and the pressure is 1.5 bar, and the temperature range of the desorption tower in the present application is 80-90°C, and the pressure is 1 bar.

[0070] Table 1 Comparison of energy consumption of different processes

[0071] Table 2 Energy consumption of gas stripping desorption in this application Note 1: The energy consumption in Table 2 is based on 150Nm 3 / h product gas is calculated; sensible heat of 40-80 includes the total energy consumption of the first heater and the second heater;

[0072] As can be seen from the results in Tables 1 and 2, the present application captures carbon dioxide from carbon-containing flue gas through a gas stripping desorption method, which can significantly reduce system energy consumption, lower the temperature of the rich liquid sent to the desorption tower 210 by the circulation unit 400, and reduce the energy consumption of the entire system. In addition, the present application uses a nitrogen membrane separator to not only separate carbon dioxide and desorbed gas, but the separated carbon dioxide can directly liquefy and store the product gas to meet the pressure without the need for a separate pressurizing device. In addition, the present application reduces the desorption pressure of carbon dioxide by sending the desorbed gas into the desorption tower 210.

[0073] In the above embodiments, the description of each embodiment has its own focus. For parts that are not described in detail in a certain embodiment, reference can be made to the relevant descriptions of other embodiments.

[0074] The above is a detailed introduction to a gas capture and storage system and method provided in the embodiments of the present application. Specific examples are used herein to illustrate the principles and implementation methods of the present application. The description of the above embodiments is only used to help understand the method of the present application and its core idea. At the same time, for those skilled in the art, based on the ideas of the present application, there may be changes in the specific implementation methods and application scope. In summary, the content of this specification should not be understood as a limitation on the present application.

[0075] Reference numerals in the figure: 100-absorption unit, 110-absorption tower 101-first inlet, 102-first outlet, 103-third inlet, 200-desorption unit, 210-desorption tower, 201-second inlet, 202-second outlet, 203-third outlet, 204-fourth inlet, 300-gas transfer unit, 301-membrane separator, 302-condenser, 303-second heater, 304-fifth inlet, 400-circulation unit, 401-first circulation pump, 402-second circulation pump, 403-heat exchanger, 4031-first heat exchange outlet, 4032-second heat exchange outlet, 404-first heater, 405-cooler.

Claims

1. A gas capture and storage system, comprising: An absorption unit (100), the absorption unit (100) having a first inlet (101) and a first outlet (102), carbon-containing flue gas is fed into the absorption unit (100) from the first inlet (101), the carbon-containing flue gas contains carbon dioxide, the carbon-containing flue gas contacts with an absorption liquid in the absorption unit (100) to form a first solution, and the first solution is fed out from the first outlet (102); A desorption unit (200), wherein the desorption unit (200) has a second inlet (201), and the first solution delivered from the first outlet (102) is delivered to the desorption unit (200) from the second inlet (201); A gas transfer unit (300), wherein the gas transfer unit (300) is used to feed a desorption gas into the desorption unit (200), wherein the desorption gas contacts the first solution to complete the desorption of at least a portion of the carbon dioxide to form a second solution, and the second solution is fed from the desorption unit (200) into the absorption unit (100).

2. The gas capture storage system according to claim 1, further comprising a circulation unit (400), wherein the circulation unit (400) comprises a first circulation pump (401), wherein the inlet of the first circulation pump (401) is connected to the first outlet (102), and the outlet of the first circulation pump (401) is connected to the second inlet (201).

3. The gas capture storage system according to claim 2, wherein: The circulation unit (400) comprises a second circulation pump (402), the absorption unit (100) has a third inlet (103), the desorption unit (200) has a second outlet (202), the inlet of the second circulation pump (402) is connected to the second outlet (202), and the outlet of the second circulation pump (402) is connected to the third inlet (103).

4. The gas capture storage system according to claim 3, wherein: The circulation unit (400) comprises a heat exchanger (403), and the heat exchanger (403) is respectively connected to an outlet of the first circulation pump (401) and an outlet of the second circulation pump (402).

5. The gas capture storage system according to claim 4, wherein: The heat exchanger (403) has a first heat exchange outlet (4031), which is connected to the second inlet (201); the heat exchanger (403) has a second heat exchange outlet (4032), which is connected to the third inlet (103).

6. The gas capture storage system according to claim 5, wherein: The circulation unit (400) includes a first heater (404), and the first heater (404) is arranged between the first heat exchange outlet (4031) and the second inlet (201).

7. The gas capture storage system according to claim 5 or 6, wherein: The circulation unit (400) comprises a cooler (405), and the cooler (405) is arranged between the second heat exchange outlet (4032) and the third inlet (103).

8. The gas capture storage system according to any one of claims 5 to 7, wherein: The gas transfer unit (300) comprises a membrane separator (301), the desorption unit (200) has a third outlet (203), and the inlet of the membrane separator (301) is in communication with the third outlet (203).

9. The gas capture storage system of claim 8, wherein: The gas transfer unit (300) comprises a condenser (302), and the condenser (302) is arranged between the membrane separator (301) and the third outlet (203).

10. The gas capture storage system according to claim 8 or 9, wherein: The gas transfer unit (300) comprises a second heater (303), the desorption unit (200) has a fourth inlet (204), and the second heater (303) is arranged between the membrane separator (301) and the fourth inlet (204).

11. A gas capture storage system according to any one of claims 8 to 10, wherein: The gas delivery unit (300) has a fifth inlet (304) for feeding a desorption gas.

12. A gas capture method comprising: The carbon-containing flue gas is fed into an absorption unit (100), wherein the absorption unit (100) contains an absorption liquid, the carbon-containing flue gas contains carbon dioxide, and the absorption liquid forms a first solution after contacting the carbon-containing flue gas; The first solution is fed into a desorption unit (200), and a gas transmission unit (300) feeds a desorption gas into the desorption unit (200) for desorbing carbon dioxide in the first solution; The first solution after desorption forms a second solution, and the second solution is sent from the desorption unit (200) to the absorption unit (100).

13. The gas capture method according to claim 12, wherein: The absorption unit (100) has a first air pressure, and the pressure range of the first air pressure is 0.8 to 1.2 bar.

14. The gas capture method according to claim 12, wherein: The absorption unit (100) has a first temperature, and the first temperature ranges from 30 to 40°C.

15. The gas capture method according to claim 12, wherein: The absorption unit (100) has a first air pressure, the pressure range of the first air pressure is 0.8-1.2 bar, and the absorption unit (100) has a first temperature, the first temperature range is 30-40°C.

16. The gas capture method according to any one of claims 12 to 15, wherein: The desorption unit (200) has a second gas pressure, and the pressure range of the second gas pressure is 0.8 to 1.2 bar.

17. The gas capture method according to any one of claims 12 to 15, wherein: The desorption unit (200) has a second temperature, and the second temperature ranges from 80 to 90°C.

18. The gas capture method according to any one of claims 12 to 15, wherein: The desorption unit (200) has a second gas pressure, the pressure range of the second gas pressure is 0.8-1.2 bar, and the desorption unit (200) has a second temperature, the second temperature range is 80-90°C.

Citation Information

Patent Citations

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