CARBON MONOXIDE PRODUCTION DEVICE, CARBON DIOXIDE ELECTROLYSIS DEVICE, AND CARBON DIOXIDE ELECTROLYSIS METHOD

Information

  • Patent Application
  • 20240360568
  • Publication Number
    20240360568
  • Date Filed
    July 11, 2024
    6 months ago
  • Date Published
    October 31, 2024
    2 months ago
  • CPC
    • C25B1/23
    • C25B9/67
    • C25B15/021
    • C25B15/085
  • International Classifications
    • C25B1/23
    • C25B9/67
    • C25B15/021
    • C25B15/08
Abstract
There are provided a CO production device and a CO2 electrolysis device which allow a promotion of effective use of CO2 and a reduction in emission of CO2 into the air. A CO production device and CO2 electrolysis device 1 of an embodiment includes: a CO2 electrolysis apparatus 3 including a cathode 6 which electrolyzes CO2 to produce CO and an anode 7 which oxidizes a substance to be oxidized to produce an oxide; a CO purifier 4 which purifies CO from a gas containing CO supplied from the CO2 electrolysis apparatus 3; and a H2 purifier 5 which purifies H2 from a CO-extracted residual gas discharged from the CO purifier.
Description
FIELD

Embodiments of the present invention relate to a carbon monoxide production device, a carbon dioxide electrolysis device, and a carbon dioxide electrolysis method.


BACKGROUND

Carbon dioxide (CO2) generated by combusting fossil fuels such as natural gas, coal, and petroleum is considered the main factor behind global warming due to a greenhouse effect, and a reduction in use of the fossil fuels is required. As large-scale generation sources of CO2, a thermal power plant, a steel plant, and the like can be cited. If CO2 is removed from an exhaust gas emitted from these CO2 generation sources and the emission into the air is reduced, the cause of global warming can be efficiently removed. Moreover, if the CO2 removed from the exhaust gas is reduced by some kinds of means and carbon compounds are produced, it can be recycled to carbon compounds similar to fuels and chemicals derived from fossil resources.


A CO2 electrolysis device (CO production device) which reduces CO2 to produce a carbon compound such as carbon monoxide (CO) is suitable for conversion of CO2 into the carbon compound such as CO. In the CO2 electrolysis device, a CO purification device which purifies CO from a gas containing CO discharged from a cathode is used. A part of a purge gas, after the CO purification, generated from a conventional CO purification device is supplied to the CO2 electrolysis device, and the remainder thereof is made harmless by air combustion to be emitted into the air. In CO2 supplied to the CO production device, CO2 supplied for purging oxygen generated from the CO2 electrolysis device, and CO2 discharged from a combustion apparatus are emitted into the air without being effectively used. Thus, a carbon monoxide production device which effectively uses the supplied CO2 to reduce the emission of CO2 into the air is required.


A problem to be solved by the present invention is to provide a carbon monoxide production device, a carbon dioxide electrolysis device, and a carbon dioxide electrolysis method which allow a promotion of effective use of CO2 and a reduction in emission of CO2 into the air.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 A diagram illustrating a carbon monoxide production device and carbon dioxide electrolysis device of an embodiment.



FIG. 2 A diagram illustrating a first modified example of the carbon monoxide production device and carbon dioxide electrolysis device illustrated in FIG. 1.



FIG. 3 A diagram illustrating a second modified example of the carbon monoxide production device and carbon dioxide electrolysis device illustrated in FIG. 1.



FIG. 4 A diagram illustrating a third modified example of the carbon monoxide production device and carbon dioxide electrolysis device illustrated in FIG. 1.





DETAILED DESCRIPTION

A carbon monoxide production device of an embodiment includes: a carbon dioxide electrolysis apparatus including a cathode which reduces carbon dioxide to produce carbon monoxide, and an anode which oxidizes a substance to be oxidized to produce an oxide; a carbon monoxide purifier which purifies carbon monoxide from a gas containing carbon monoxide supplied from the cathode of the carbon dioxide electrolysis apparatus; and a hydrogen purifier which purifies hydrogen from a carbon monoxide-extracted residual gas discharged from the carbon monoxide purifier.


Hereinafter, a carbon monoxide production device, a carbon dioxide electrolysis device, and a carbon dioxide electrolysis method of embodiments will be described with reference to the drawings. In each embodiment presented below, substantially the same constituent parts are denoted by the same reference signs, and a description thereof may be partially omitted. The drawings are schematic, and the relation of the thickness and planar dimension, a thickness ratio among the parts, and so on may be different from actual ones. Note that a symbol of “˜” in the following description indicates a range between an upper limit value and a lower limit value of the respective numerical values. In this case, the range of the numerical values includes the upper limit value and the lower limit value.



FIG. 1 is a diagram illustrating a carbon monoxide production device and carbon dioxide electrolysis device of the embodiment. A carbon monoxide (CO) production device and carbon dioxide (CO2) electrolysis device 1 illustrated in FIG. 1 includes a CO2 recovery apparatus 2 which recovers CO2 from a gas containing carbon dioxide (CO2), a CO2 electrolysis apparatus 3 which electrolyzes and reduces CO2 to produce carbon monoxide (CO), a CO purifier 4 which purifies CO from a gas containing CO supplied from the CO2 electrolysis apparatus 3, and a H2 purifier 5 which purifies hydrogen (H2) from a CO-extracted residual gas discharged from the CO purifier 4.


The CO2 recovery apparatus 2 is configured to separate and recover CO2 from an emission gas G1 containing CO2 (a gas containing CO2) emitted from a thermal power plant, a waste incineration plant, a steel plant, and the like, and supply a CO2 gas G2 whose CO2 concentration has been increased to the CO2 electrolysis apparatus 3. To the separation and recovery of CO2, for example, a chemical absorption method of using a chemical absorption solution such as an amine aqueous solution, a solid absorption method of using a solid absorbent such as an amine compound, a membrane separation method of using a CO2 separation membrane, a physical adsorption method of using an inorganic substance such as zeolite as an adsorbent, or the like is applied. For example, in the chemical absorption method and device which use the amine aqueous solution, the emission gas G1 is supplied to an absorption tower in which the amine aqueous solution is sprayed, the amine aqueous solution absorbing CO2 is heated in a regeneration tower, and CO2 diffused from the amine aqueous solution is recovered. The CO2 recovery method and device applied to the CO2 recovery apparatus 2 are not particularly limited, and various methods and devices which allow the recovery of CO2 from the emission gas G1 can be applied.


The CO2 electrolysis apparatus 3 is a CO2 electrolysis device having an electrolysis cell, and includes a cathode 6 and an anode 7. The cathode 6 includes a reduction electrode (cathode), the anode 7 includes an oxidation electrode (anode), and an electrolytic solution is made to flow through or fills at least the anode 7. A CO2 gas may be made to flow through the cathode 6, or an electrolytic solution containing CO2 may be made to flow through or may fill it. In the cathode 6 or the anode 7, for example, for the electrolytic solution, a solution using water (H2O), for example, an aqueous solution containing an optional electrolyte can be used. As the aqueous solution containing the electrolyte, there can be cited an aqueous solution containing, for example, phosphate ions (PO42−), borate ions (BO33−), sodium ions (Na+), potassium ions (K+), calcium ions (Ca2+), lithium ions (Li+), cesium ions (Cs+), magnesium ions (Mg2+), chloride ions (Cl), hydrogen carbonate ions (HCO3), carbonate ions (CO32−), hydroxide ions (OH), or the like. As a concrete example of the electrolytic solution, an alkaline aqueous solution in which KOH, KHCO3, K2CO3, or the like is dissolved can be cited.


To the cathode 6, the CO2 gas G2 recovered in the CO2 recovery apparatus 2 is supplied. As described in detail later, to the cathode 6, a CO2 gas as a H2-extracted residual gas discharged from the H2 purifier 5 is supplied in addition to the CO2 gas G2. The cathode 6 has a non-illustrated gas flow path, and the CO2 gas is supplied to such a gas flow path facing the reduction electrode. The anode 7 has a non-illustrated liquid flow path, for example, and the electrolytic solution is supplied to such a liquid flow path facing the oxidation electrode. A non-illustrated power supply is connected to the reduction electrode and the oxidation electrode. The cathode 6 and the anode 7 are separated by a membrane 8 capable of moving ions of hydrogen ions (H+), hydroxide ions (OH), carbonate ions (CO32−), hydrogen carbonate ions (HCO3), or the like, for example, an ion exchange membrane. The CO2 electrolysis apparatus 3 (the CO2 electrolysis device having the electrolysis cell) may have a single electrolysis cell, a configuration to connect electrolysis cells in a plane direction, or a configuration to stack and integrate a plurality of the electrolysis cells.


In the cathode 6 and the anode 7 of the CO2 electrolysis apparatus 3, the reactions as presented below occur. In the cathode 6, as presented in the following formula (1), an electrolytic reaction and a reduction reaction of CO2 occur. CO and a carbonate ion (CO32−) are produced by the reduction reaction of CO2.




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The carbonate ion (CO32−) produced in the cathode 6 moves to the anode 7 via the membrane 8. In the anode 7, as presented in the following formula (2), an oxidation reaction of the carbonate ion (CO32−) produced in the cathode 6 occurs, and CO2 and O2 are produced.




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Moreover, in the cathode 6, an electrolytic reaction of H2O in the electrolytic solution occurs, and as presented in the following formula (3), hydrogen (H2) and hydroxide ions (OH) are produced.




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The produced hydroxide ions (OH) move to the anode 7 via the membrane 8, and as presented in the following formula (4), water (H2O) and oxygen (O2) are produced in the anode 7.




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Further, in the anode 7, as presented in the following formula (5), water (H2O) in the electrolytic solution is electrolyzed, and oxygen (O2) and hydrogen ions (H+) are produced.




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The produced hydrogen ions (H+) move to the cathode 6 via the membrane 8. In the cathode 6 which the hydrogen ions (H+) reach and in which electrons (e) reach the cathode through an external circuit, hydrogen is produced by a reaction presented in the following formula (6).




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In the cathode 6, CO is produced by the reduction of CO2 as presented in the formula (1), and H2 is produced by the electrolytic reaction of H2O as presented in the formula (3). The CO and H2 produced in the cathode 6 are discharged from the cathode 6 with unreacted CO2. A mixed gas G3, discharged from the cathode 6, containing CO and H2 and CO2 is supplied to the CO purifier 4. In the CO purifier 4, CO is purified from the mixed gas G3 containing CO and H2 and CO2. For the purification of CO (separation of CO), for example, a pressure swing adsorption method (PSA method) of using CO adsorption and desorption caused by pressure fluctuations of an adsorbent to separate and recover CO by adsorbing CO under pressurization and desorbing CO under depressurization, specifically, a CO-PSA separation and purification device using an adsorbent in which monovalent copper is supported on alumina, or the like, can be applied, and these are not particularly restrictive.


A CO gas G4 separated and recovered in the CO purifier 4 is supplied to, for example, a carbon-containing liquid fuel synthesis device using a Fischer-Tropsch synthesis reaction, or the like, which is not illustrated in FIG. 1, as a fuel component. A residual gas, discharged from the CO purifier 4, subjected to the separation and recovery of CO, that is, a CO-extracted residual gas G5 contains H2 and CO2. Such a CO-extracted residual gas G5 is supplied to the hydrogen (H2) purifier 5. In the H2 purifier 5, H2 is purified from the mixed gas G5 containing H2 and CO2. For the purification of H2 (separation of H2), for example, a H2 separation and purification device applying a H2-PSA method of using H2 adsorption and desorption caused by pressure fluctuations of an adsorbent to separate and recover H2 by adsorbing H2 under pressurization and desorbing H2 under depressurization, or a H2 separation device using a H2 separation membrane which selectively transmits H2 can be applied, and these are not particularly restrictive. A H2 gas G6 separated and recovered in the H2 purifier 5 is used as a fuel for various devices of a fuel cell vehicle or the like and a fuel component in liquid fuel synthesis devices or the like although they are not illustrated in FIG. 1. For example, in the above-described carbon-containing liquid fuel synthesis device using the Fischer-Tropsch synthesis reaction, H2 is used with CO, and thus may be supplied to such liquid fuel synthesis devices as a part of the fuel component. Moreover, the H2 gas G6 separated and recovered in the H2 purifier 5 may be stored in a tank or the like ones. A residual gas, discharged from the H2 purifier 5, subjected to the separation and recovery of H2, that is, a H2-extracted residual gas G7 contains CO2. CO and H2 are separated and recovered from the mixed gas G3, and thus purity of CO2 increases. Accordingly, the H2-extracted residual gas G7 containing CO2 can be supplied to the cathode 6 of the CO2 electrolysis apparatus 3. Thus, use efficiency of CO2 can be enhanced.


As described above, supplying the mixed gas G3, discharged from the cathode 6, containing CO and H2 and CO2 to the CO purifier 4 and the H2 purifier 5 in order, and separating and recovering CO and separating and recovering H2 allow not only a promotion of effective use of CO and H2 but also effective use of a CO2 gas as the residual gas G7 subjected to separation and recovery of CO and H2 from the mixed gas G3. Specifically, in the CO production device 1 of the embodiment, the H2-extracted residual gas G7 containing CO2 is supplied to the cathode 6 of the CO2 electrolysis apparatus 3, and thus the CO2 gas (G7) can be effectively used without being emitted into the air.


In FIG. 1, the CO2 gas as the H2-extracted residual gas G7 is directly supplied to the cathode 6 of the CO2 electrolysis apparatus 3, and this is not restrictive. For example, in a case where the CO2 recovery apparatus 2 has a flow rate regulating mechanism of a CO2 gas, or the like, as illustrated in FIG. 2, the CO2 gas G7 may be supplied to the CO2 recovery apparatus 2 and mixed with the CO2 gas recovered in the CO2 recovery apparatus 2 to be supplied to the cathode 6 of the CO2 electrolysis apparatus 3. In this case, a flow rate is regulated in the CO2 recovery apparatus 2, and the CO2 gas is supplied to the cathode 6 of the CO2 electrolysis apparatus 3. Alternatively, as illustrated in FIG. 3, for example, a CO2 supply device 9 which stores the CO2 gas once and regulates a flow rate of the stored CO2 gas to supply it to the cathode 6 may be provided between the CO2 recovery apparatus 2 and the cathode 6 of the CO2 electrolysis apparatus 3, and the CO2 gas may be supplied to such a CO2 supply device 9.


In the anode 7 of the CO2 electrolysis apparatus 3, as presented in the formula (2) and the formula (4), oxygen (O2) and carbon dioxide (CO2) are produced by the oxidation of a carbonate ion (CO32−) and the oxidation of hydroxide ions (OH). The O2 and CO2 produced in the anode 7 are discharged from the anode 7. A mixed gas G8, discharged from the anode 7, containing O2 and CO2 is supplied to the CO2 recovery apparatus 2. The electrolysis cell as the CO2 electrolysis apparatus 3 is operated at a temperature of, for example, approximately 80° C. Accordingly, a temperature of the mixed gas G8 discharged from the anode 7 may be approximately 80° C. The mixed gas G8 with such a temperature may adversely affect the CO2 recovery device using, for example, an amine aqueous solution when directly supplied to the CO2 recovery apparatus 2. Therefore, as illustrated in FIG. 4, a cooler 10 may be provided in a pipe which supplies the mixed gas G8 from the anode 7 to the CO2 recovery apparatus 2. By supplying a mixed gas G9 cooled by the cooler 10 to the CO2 recovery apparatus 2, recovery efficiency of CO2 by using the CO2 recovery apparatus 2 can be maintained.


As described above, CO2 in the mixed gas G8 discharged from the anode 7 is recovered in the CO2 recovery apparatus 2 similarly to CO2 in the emission gas (a gas containing CO2) G1. Accordingly, the CO2 discharged from the anode 7 can also be effectively used similarly to CO2 discharged from the cathode 6. These make it possible to reuse unreacted CO2 discharged from the cathode 6 and the CO2 reproduced in the anode 7 in addition to the recovery of CO and H2 produced in the cathode 6. Consequently, CO, H2, and most of CO2 as the produced gases and the emission gas in the CO production device 1 can be effectively used or reused. For example, without emitting the unreacted CO2 or the reproduced CO2 into the air, the use efficiency of CO2 can be greatly enhanced. Although a reaction mechanism is different, a configuration of the above-described electrolysis device is also applicable to a solid oxide eletrolyzer cell (SOEC) which performs supply of a CO2 gas or a CO2/H2 mixed gas to a cathode and/or supply of a CO2 gas to an anode.


Note that the configurations of the above-described embodiments are applicable in combination with each other, and parts thereof are also replaceable. While certain embodiments of the present invention have been described above, these embodiments have been presented by way of example only, and are not intended to limit the scope of the invention. Indeed these embodiments described herein may be embodied in a variety of other forms; furthermore, various omissions, substitutions, and changes in the form of the embodiments described herein may be made without departing from the spirit of the inventions. The accompanying claims and their equivalents are intended to cover such forms or modifications as would fall within the scope and spirit of the inventions.


EXPLANATION OF REFERENCE SIGNS






    • 1 . . . . CO production device, 2 . . . . CO2 recovery apparatus, 3 . . . . CO2 electrolysis apparatus, 4 . . . . CO purifier, 5 . . . . H2 purifier, 6 . . . cathode, 7 . . . anode, 8 . . . membrane, 9 . . . . CO2 supply device, 10 . . . cooler.




Claims
  • 1. A carbon monoxide production device comprising: a carbon dioxide electrolysis apparatus including a cathode for reducing carbon dioxide to produce carbon monoxide, and an anode for oxidizing a substance to be oxidized to produce an oxide;a carbon monoxide purifier configured to purify carbon monoxide from a gas containing carbon monoxide supplied from the cathode of the carbon dioxide electrolysis apparatus; anda hydrogen purifier configured to purify hydrogen from a carbon monoxide-extracted residual gas discharged from the carbon monoxide purifier.
  • 2. The carbon monoxide production device according to claim 1, wherein the hydrogen purifier is configured to discharge a hydrogen-extracted residual gas containing carbon dioxide and supply the hydrogen-extracted residual gas to the cathode of the carbon dioxide electrolysis apparatus.
  • 3. The carbon monoxide production device according to claim 1, further comprising a carbon dioxide recovery apparatus configured to recover carbon dioxide from a gas containing carbon dioxide and supply the recovered carbon dioxide to the cathode of the carbon dioxide electrolysis apparatus.
  • 4. The carbon monoxide production device according to claim 3, wherein the carbon dioxide electrolysis apparatus is configured to supply a gas, discharged from the anode, containing carbon dioxide to the carbon dioxide recovery apparatus.
  • 5. The carbon monoxide production device according to claim 4, further comprising a cooler configured to cool the gas discharged from the anode of the carbon dioxide electrolysis apparatus and supply the cooled gas to the carbon dioxide recovery apparatus.
  • 6. A carbon dioxide electrolysis device comprising: a carbon dioxide electrolysis apparatus including a cathode for reducing carbon dioxide to produce carbon monoxide, and an anode for oxidizing a substance to be oxidized to produce an oxide;a carbon monoxide purifier configured to purify carbon monoxide from a gas containing carbon monoxide supplied from the cathode of the carbon dioxide electrolysis apparatus; anda hydrogen purifier configured to purify hydrogen from a carbon monoxide-extracted residual gas discharged from the carbon monoxide purifier.
  • 7. The carbon dioxide electrolysis device according to claim 6, wherein the hydrogen purifier is configured to discharge a hydrogen-extracted residual gas containing carbon dioxide and supply the hydrogen-extracted residual gas to the cathode of the carbon dioxide electrolysis apparatus.
  • 8. The carbon dioxide electrolysis device according to claim 6, further comprising a carbon dioxide recovery apparatus configured to recover carbon dioxide from a gas containing carbon dioxide and supply the recovered carbon dioxide to the cathode of the carbon dioxide electrolysis apparatus.
  • 9. The carbon dioxide electrolysis device according to claim 8, wherein the carbon dioxide electrolysis apparatus is configured to supply a gas, discharged from the anode, containing carbon dioxide to the carbon dioxide recovery apparatus.
  • 10. The carbon dioxide electrolysis device according to claim 9, further comprising a cooler configured to cool the gas discharged from the anode of the carbon dioxide electrolysis apparatus and supply the cooled gas to the carbon dioxide recovery apparatus.
  • 11. A carbon dioxide electrolysis method comprising the steps of: reducing carbon dioxide to produce carbon monoxide in a cathode, and oxidizing a substance to be oxidized to produce an oxide in an anode;purifying carbon monoxide from a gas containing carbon monoxide supplied from the cathode; andpurifying hydrogen from a carbon monoxide-extracted residual gas after purifying carbon monoxide from the gas containing carbon monoxide.
  • 12. The carbon dioxide electrolysis method according to claim 11, further comprising the step of supplying a hydrogen-extracted residual gas, after purifying hydrogen from the carbon monoxide-extracted residual gas, containing carbon dioxide to the cathode.
  • 13. The carbon dioxide electrolysis method according to claim 11, further comprising the step of recovering carbon dioxide from a gas containing carbon dioxide in a carbon dioxide recovery apparatus and supplying the recovered carbon dioxide to the cathode.
  • 14. The carbon dioxide electrolysis method according to claim 13, comprising the step of supplying a gas, discharged from the anode, containing carbon dioxide to the carbon dioxide recovery apparatus.
  • 15. The carbon dioxide electrolysis method according to claim 14, further comprising the step of cooling the gas discharged from the anode and supplying the cooled gas to the carbon dioxide recovery apparatus.
Priority Claims (1)
Number Date Country Kind
2022-087736 May 2022 JP national
CROSS REFERENCE TO RELATED APPLICATION

The present application is a continuation application of International Application No. PCT/JP2023/003066, filed Jan. 31, 2023, which is based upon and claims the benefit of priority from Japanese Patent Application No. 2022-087736, filed May 30, 2022; the entire contents of all of which are incorporated herein by reference.

Continuations (1)
Number Date Country
Parent PCT/JP2023/003066 Jan 2023 WO
Child 18769484 US