TECHNICAL FIELD
Cross-reference to Related Applications
Technical Field
[0002] The present invention relates to an electrolysis device for electrochemically reducing
carbon dioxide.
BACKGROUND ART
[0003] Carbon dioxide is a greenhouse gas that causes global warming, and thus, should be
reduced. As a method for reducing carbon dioxide, methods such as capture, chemical
conversion, or electrochemical conversion are known. Among the above-described methods,
the electrochemical conversion method allows for a precise control of components so
as to produce other synthetic gases, and is thus more economically beneficial than
simply removing carbon dioxide. In addition, carbon dioxide may be electrolyzed together
with water to obtain carbon monoxide, ethylene, methane, formic acid, formate, various
hydrocarbons, and an organic substance such as an aldehyde or an alcohol.
[0004] A process of electrochemically decomposing carbon dioxide is similar to a technique
of electrolyzing water. However, since the activity of an electrochemical reaction
improves in a strong base atmosphere, an aqueous KOH solution of a certain concentration
is generally used as an electrolyte solution. When a current is applied while supplying
water to an anode, the water is decomposed into a hydrogen ion and an electron together
with the generation of oxygen gas. The electron is transferred to a cathode through
an external conductive line, and the hydrogen ion is transferred to the cathode through
an ion-selective separation membrane. At this time, the transferred electron reacts
with carbon dioxide and water supplied to the cathode and then is decomposed into
carbon monoxide and a hydroxide ion (OH
-), and the generated hydroxide ion reacts with a hydrogen ion (H
+) of an anode to produce water, thereby being in an electrical neutral state. Through
the above process, an electrochemical decomposition reaction of carbon dioxide is
completed. At this time, the water supplied together with the carbon dioxide reacts
with the transferred electron, which is separate from the carbon monoxide production
reaction, and is electrolyzed, thereby producing hydrogen gas, and at the same time,
producing a hydroxide ion. Such a reaction of water and an electron may be said to
have a competitive relationship with the carbon monoxide production reaction. Since
the reactions are electrochemical reactions, the generation amount of carbon monoxide
and a ratio of hydrogen/carbon dioxide may be easily controlled by controlling a voltage.
[0005] Meanwhile, in a typical electrolysis device, OH
- is produced by a side reaction in a cathode during a carbon dioxide electrolysis
process, and the OH
- is reacted again with supplied carbon dioxide and produces a carbonate (HCO
3-). Therefore, the typical electrolysis device has a problem in that supplied carbon
dioxide produces a carbonate without being converted into a desired product, which
results in causing the loss of the carbon dioxide. In addition, the typical electrolysis
device has a problem in that the efficiency of the electrolysis is reduced since the
carbonate is diffused into an anode by passing through an anion exchange membrane
and carbon dioxide is produced through an oxidation reaction in the anode.
(Patent Document 001) KR 10-2018-0133688 A
DISCLOSURE OF THE INVENTION
TECHNICAL PROBLEM
[0006] An object to be achieved by the present invention is to provide an electrolysis device
in which carbon dioxide is separated again from a carbonate produced by a side reaction
during electrolysis of carbon dioxide, thereby preventing the loss of carbon dioxide
converted into a carbonate and improving the yield of a product.
TECHNICAL SOLUTION
[0007] The present invention provides an electrolysis device.
- (1) The present invention provides an electrolysis device including an electrolysis
cell having a gas diffusion layer, a cathode, a separation membrane, an anode, and
an electrolyte solution, and outside the electrolysis cell, an acid solution reservoir
connected by a discharge flow path for discharging a product from the cathode, wherein
the separation membrane is a cation separation membrane.
- (2) In (1) above, the present invention provides an electrolysis device, wherein the
acid solution reservoir includes an acidic solution containing one or more selected
from the group consisting of phosphoric acid, hydrochloric acid, sulfuric acid, nitric
acid, acetic acid, citric acid, and oxalic acid.
- (3) In (1) or (2) above, the present invention provides an electrolysis device, wherein
the electrolyte solution is an aqueous solution containing one or more selected from
the group consisting of Cs2CO3, CsHCO3, Cs2SO4, CsCl, CsNO3, K2CO3, KHCO3, K2SO4, K3PO4, KCl, KNO3, Na2CO3, NaHCO3, Na2SO4, Na3PO4, NaCl, and NaNO3.
- (4) In any one of (1) to (3) above, the present invention provides an electrolysis
device, wherein the electrolysis cell is a zero-gap membrane electrode assembly cell
in which the gas diffusion layer, the cathode, the separation membrane, and an anode
with an anode liquid flow path formed therein are sequentially stacked.
- (5) In any one of (1) to (4) above, the present invention provides an electrolysis
device, wherein a product produced by an electrolysis reaction in the cathode is transferred
to the acid solution reservoir through the discharge flow path, wherein the product
includes carbon monoxide, water vapor, and a salt.
- (6) In (5) above, the present invention provides an electrolysis device, wherein carbon
dioxide produced from the salt in the acid solution reservoir is supplied to the electrolysis
cell.
- (7) In (5) or (6) above, the present invention provides an electrolysis device, wherein
the salt is a carbonate.
- (8) In any one of (1) to (7) above, the present invention provides an electrolysis
device, wherein the electrolysis device electrolyzes carbon dioxide.
- (9) In (8) above, the present invention provides an electrolysis device, wherein the
carbon dioxide is supplied in a state including water vapor when supplied to the electrolysis
cell.
- (10) In any one of (1) to (9) above, the present invention provides an electrolysis
device, wherein the electrolysis device electrolyzes carbon dioxide, thereby producing
one or more selected from the group consisting of carbon monoxide, ethylene, methane,
formic acid, hydrocarbon, aldehyde, and alcohol.
ADVANTAGEOUS EFFECTS
[0008] An electrolysis device of the present invention connects an acid solution reservoir
with an electrolysis cell, thereby separating carbon dioxide from a salt produced
by a side reaction in the acid solution reservoir, and thus, may prevent the loss
of carbon dioxide.
[0009] In addition, the electrolysis device of the present invention reduces the loss of
carbon dioxide, and thus, may improve the electrolysis efficiency of carbon dioxide,
thereby increasing the yield of a product.
BRIEF DESCRIPTION OF THE DRAWING
[0010] FIG. 1 is a schematic diagram of a carbon dioxide electrolysis device according to
the present invention.
MDOE FOR CARRYING OUT THE INVENTION
[0011] Hereinafter, the present invention will be described in more detail to facilitate
understanding of the present invention. In this case, it will be understood that words
or terms used in the specification and claims shall not be interpreted as having the
meaning defined in commonly used dictionaries. It will be further understood that
the words or terms should be interpreted as having a meaning that is consistent with
their meaning in the context of the relevant art and the technical idea of the invention,
based on the principle that an inventor may properly define the meaning of the words
or terms to best explain the invention.
[0012] The terms used herein are only used to describe exemplary embodiments, and are not
intended to limit the present invention. Singular expressions include plural expressions
unless the context clearly indicates otherwise.
[0013] It will be further understood that the terms "include," "comprise," or "have" when
used in the present specification, specify the presence of stated features, numbers,
steps, elements, or combinations thereof, but do not preclude the presence or addition
of one or more other features, numbers, steps, elements, or combinations thereof.
[0014] The present invention provides an electrolysis device including an electrolysis cell
having a gas diffusion layer, a cathode 13, a separation membrane 15, an anode 11,
and an electrolyte solution, and outside the electrolysis cell, an acid solution reservoir
20 connected by a discharge flow path 30 for discharging a product from the cathode
13, wherein the separation membrane 15 is a cation separation membrane.
[0015] According to an embodiment of the present invention, the electrolysis device may
be used in all fields of electrochemical conversion, and the electrolysis device may
be a fuel cell, a device capable of producing useful chemical materials through electrochemical
conversion such as water electrolysis, or a device which may be utilized for reducing
and converting carbon dioxide and NOx. Specifically, the electrolysis device may be
an electrochemical conversion device which converts carbon dioxide into carbon monoxide
and ethylene.
[0016] As described in the background art, an electrolysis cell having a typical structure
in which an electrolyte solution flows in the front part of a cathode has a problem
in that OH
- produced by a side reaction during a reduction process of carbon dioxide reacts again
with the carbon dioxide to produce a carbonate (HCO
3-), and thus, the carbon dioxide is lost, wherein the problem is solvable by allowing
an acidic electrolyte solution to flow in the front part of the cathode, but in this
case, additional resistance occurs by the acidic electrolyte solution, which creates
an additional problem in which a voltage increases. In addition, as a separation membrane
to be included in a carbon dioxide electrolysis cell, an anion exchange membrane has
been mainly used, and the anion exchange membrane is fast in ion transfer, and thus,
has excellent carbon dioxide conversion efficiency, but has very low mechanical strength,
and in addition, the carbonate passes through the anion exchange membrane and is diffused
to an anode and carbon dioxide is produced through an oxidation reaction in the anode,
so that there is a problem in that the efficiency of the electrolysis is degraded.
[0017] Therefore, the inventor of the present invention developed an electrolysis device
of the present invention in which a produced carbonate is not diffused into the anode
11, and carbon dioxide is separated again from the produced carbonate, thereby reducing
the loss of supplied carbon dioxide. Specifically, the electrolysis device includes
the electrolysis cell and the acid solution reservoir 20 connected to the outside
of the electrolysis cell. The electrolysis device includes the cathode 13 and the
anode 11, wherein the gas diffusion layer may be disposed in close proximity to the
cathode 13, and may include the separation membrane 15 disposed between the cathode
13 and the anode 11 and the electrolyte solution together. In addition, the electrolysis
device according to the present invention may include an electrolysis cell having
a structure of a zero-gap membrane electrode assembly to be described later. The electrolysis
cell having a structure of a zero-gap membrane electrode assembly has a structure
in which an electrolyte solution does not flow in the front part of the cathode 13,
but the electrolyte solution flows only in the front part of the anode 11, so that
the additional problem in which a voltage increases during an electrolysis reaction
may be solved. In addition, the electrolysis cell may include a cation exchange membrane
to prevent the produced carbonate from being transported toward the anode 11.
[0018] FIG. 1 is a schematic diagram of a carbon dioxide electrolysis device according to
the present invention.
[0019] According to an embodiment of the present invention, the cathode 13 is connected
to a supply line to which a reactant is supplied, and the discharge flow path 30 through
which a product produced after electrolysis is discharged. The reactant may be carbon
dioxide, and the carbon dioxide may be in a gaseous state, and may include water vapor
of about 40 °C to 60 °C. In addition, the product is produced by electrolyzing the
carbon dioxide, and may be one or more selected from the group consisting of carbon
monoxide, ethylene, methane, formic acid, hydrocarbon, aldehyde, and alcohol. Unreacted
carbon dioxide, the water vapor, and the carbonate produced by a side reaction may
be further discharged together with the product discharged from the discharge flow
path 30.
[0020] Referring to FIG. 1, the acid solution reservoir 20 is connected to the discharge
flow path 30, and carbon dioxide may be separated again from the carbonate by an acidic
solution filled in the acid solution reservoir 20. Specifically, hydrogen ions (H
+) of the acidic solution contained in the acid solution reservoir 20 and a carbonate
(HCO
3-) may react to each other to produce water and carbon dioxide. In addition, the acid
solution reservoir 20 may include an acidic solution containing one or more selected
from the group consisting of phosphoric acid, hydrochloric acid, sulfuric acid, nitric
acid, acetic acid, citric acid, and oxalic acid. The acidic solution may serve to
reproduce carbon dioxide by reacting with a produced carbonate, and compared to a
typical electrolysis device, the electrolysis device of the present invention further
includes the acid solution reservoir 20 to reproduce carbon dioxide from a carbonate,
and thus, may improve electrolysis efficiency and reduce the amount of carbon dioxide
lost to the carbonate.
[0021] According to an embodiment of the present invention, the separation membrane 15 is
a cation separation membrane 15, and specifically, may be a Nafion separation membrane
15. The cation separation membrane 15 may serve to prevent a carbonate produced from
the cathode 13 from diffusing toward the anode 11. Furthermore, if the separation
membrane 15 is an anion separation membrane 15, a carbonate is diffused toward the
anode 11, so that the transport of the carbonate to the acid solution reservoir 20
is not facilitated, which may degrade overall electrolysis efficiency, and may increase
carbon dioxide loss.
[0022] According to an embodiment of the present invention, the electrolyte solution may
be an acidic or neutral electrolyte solution, and may be an aqueous solution containing
cations (Na
+, K
+, or Cs
+). Illustratively, it may be Cs
2CO
3, CsHCO
3, Cs
2SO
4, CsCl, CsNO
3, K
2CO
3, KHCO
3, K
2SO
4, K
3PO
4, KCl, KNO
3, Na
2CO
3, NaHCO
3, Na
2SO
4, Na
3PO
4, NaCl, or NaNO
3.
[0023] According to an embodiment of the present invention, the electrolysis cell may be
a zero-gap membrane electrode assembly cell in which the gas diffusion layer, the
cathode 13, the separation membrane 15, and the anode 11 having a liquid flow path
of the anode 11 are sequentially stacked. Specifically, in order to increase a driving
voltage and current efficiency, the zero-gap membrane electrode assembly may be formed
in a very thin valve shape in which the gas diffusion layer, the cathode 13, the separation
membrane 15, and the anode 11 having a liquid flow path of the anode 11 are sequentially
stacked.
[0024] A typical electrolysis cell has a shape of a gap structure since an electrode and
a separation membrane are spaced apart from each other by several mm intervals, but
the above-described zero gap is an electrolysis cell of a sandwich shape without an
interval between an electrode and a separation membrane since a cathode electrode
and an anode electrode are in contact with each other with a separation membrane interposed
therebetween, so that the electrolytic cell of a zero-gap shape may decrease solution
ion resistance due to the presence of an electrolyte, and may reduce an increase in
mass transfer resistance due to a produced gas when implementing a large-area electrode.
[0025] In addition, an electrolyte solution flowing toward the cathode 13 is called a cathode
13 liquid, and an electrolyte solution flowing toward the anode 11 is called an anode
11 liquid, and the zero-gap membrane electrode assembly may not include the cathode
13 liquid, but may include only the anode 11 liquid. The zero-gap membrane electrode
assembly minimizes the gap between the cathode 13, the anode 11, and the separation
membrane 15, and thus, may have the advantage of being able to accelerate the transport
of ions, decrease overvoltage, and increase current efficiency. In addition, in this
case, separation plates may be disposed on both sides of the zero-gap membrane electrode
assembly to form one cell.
[0026] According to an embodiment of the present invention, the discharge flow path 30 transports
a product produced in the cathode 13 by an electrolysis reaction to the acid solution
reservoir 20, and the product may include carbon dioxide, carbon monoxide, water vapor,
and a salt. In addition, the carbon dioxide produced in the acid solution reservoir
20 may be supplied to the electrolysis cell.
[0027] The carbon dioxide produced by separating carbon dioxide from a carbonate in the
acid solution reservoir 20 may be supplied back to the cathode 13 through a supply
line. The electrolysis device of the present invention separates carbon dioxide from
a carbonate by means of the acid solution reservoir 20, and circulates the carbon
dioxide into the electrolysis cell to reduce the loss of carbon dioxide, and to increase
electrolysis efficiency.
[0028] Hereinafter, the decomposition principle of the electrolysis device and each component
of the electrolysis device will be described.
[0029] The electrolysis refers to decomposing a material through a redox reaction by applying
a direct current voltage to perform a decomposition reaction which does not occur
spontaneously. The anode is an oxidation electrode which oxidizes water to produce
oxygen, at which time, a hydrogen ion is produced. The hydrogen ion produced in the
anode is transferred to the cathode through the electrolyte solution, and the cathode
is a reduction electrode in which a reactant introduced into the cathode may react
with an electron the hydrogen ions transferred from the anode and produce a product.
In addition, the separation membrane may be disposed between the anode and the cathode.
The separation membrane itself may be composed of an inert material that does not
participate in an electrochemical reaction, but provides a path for allowing an ion
to be transferred between the anode and the cathode, and may serve to separate a physical
contact of the anode and the cathode.
[0030] In addition, the anode and the cathode of the electrolysis device of the present
invention may each include a catalyst layer. In addition, in the cathode region, water
vapor supplied with carbon dioxide generates a reduction product by an electroreduction
reaction on the surface of the cathode. Thus, the cathode may include a gas diffusion
layer to evenly supply humidified carbon dioxide gas to the cathode region. If the
cathode includes a hydrophobic gas diffusion layer, it is possible to smoothly diffuse,
distribute, and supply supplied carbon dioxide to the catalyst layer of the cathode.
In addition, the hydrophobic gas diffusion layer effectively prevents moisture condensation,
thereby allowing the supply of carbon dioxide to be continuously uniform, and at the
same time, allowing an electrolysis reaction to smoothly progress. In addition, the
catalyst layer may have a surface having a porous structure or the like to well exert
gas permeation properties on the surface.
[0031] According to an embodiment of the present invention, the anode may include a catalyst
active in the electrolysis of water, and the catalyst layer of the anode may include
one or more selected from the group consisting of Pt, Au, Pd, Ir, Ag, Rh, Ru, Ni,
Al, Mo, Cr, Cu, Ti, W, an alloy thereof, or a mixed metal oxide, e.g., Ta
20
5, Ir0
2, etc., for an oxygen generation reaction. Specifically, in the electrolysis device
of the present invention, the anode may include titanium (Ti) coated with an iridium
oxide (IrO
2).
[0032] In addition, since a carbon dioxide reduction reaction which occurs in the cathode
competes with a hydrogen generation reaction, a voltage required for the hydrogen
generation reaction is high and a catalyst active in the carbon dioxide reduction
reaction may be included. The catalyst layer of the cathode may include one or more
selected from the group consisting of Sn, an Sn alloy, Al, Au, Ag, C, Cd, Co, Cr,
Cu, a Cu alloy, Ga, Hg, In, Mo, Nb, Ni, NiCo
2O
4, an Ni alloy, an Ni-Fe alloy, Pb, Rh, Ti, V, W, Zn, and a mixture thereof. Specifically,
in the electrolysis device of the present invention, the cathode may contain silver
(Ag).
[0033] In addition, the separation membrane, as described above, may include a cation exchange
membrane CEM, and specifically, may be a Nafion exchange membrane. The cation exchange
membrane may serve as a membrane which prevents a reduction material generated in
the cathode by catalysis from being transferred to the anode and oxidized, and may
be a separation phase which suppresses transmission of an anion and allows the transmission
of a cation such as a hydrogen ion (H
+).
[0034] In addition, the electrolyte solution, as described above, may be an electrolyte
solution according to the present invention, and specifically, may be an acidic electrolyte
solution, and more specifically, may be an aqueous solution containing cesium hydrocarbonate.
The electrolyte solution composition may include the electrolyte solution in 0.1 M
to 15.0 M, preferably 0.25 M to 10.0 M. The concentration of the electrolyte solution
is related to the production efficiency of a product (production efficiency of a target
product relative to an applied current density) and a voltage. The higher the concentration
of the electrolyte solution, the lower the generated voltage, required voltage, or
overvoltage, but the above-described conditions are preferable in order to minimize
an increase in manufacturing cost and production of additional products due to a side
reaction.
[0035] In addition, the gas diffusion layer may use a porous body using a carbon material
such as carbon fiber cloth, carbon fiber felt, carbon fiber paper, or the like, or
a metal porous body made of a thin metal plate having a net structure such as expanded
metal, metal mesh, or the like, and in the electrolysis device of the present invention,
the gas diffusion layer may use carbon fiber cloth.
[0036] According to an embodiment of the present invention, the electrolysis device may
be utilized in all fields that require electrochemical conversion, and particularly,
allows a desired product to be obtained by electrochemically decomposing carbon dioxide,
and specifically, the electrolysis device may electrolyze carbon dioxide to produce
one or more selected from the group consisting of carbon monoxide, ethylene, methane,
formic acid, hydrocarbon, aldehyde, and alcohol.
[0037] Hereinafter, embodiments of the present invention will be described in detail so
that those skilled in the art may easily carry out the present invention. However,
the present invention may be embodied in many different forms, and is not limited
to the embodiments set forth herein.
Example 1
[0038] A carbon dioxide electrolysis device having operating conditions described below
was operated. A carbon dioxide electrolysis device was operated, which is a membrane
electrode assembly having a zero-gap structure in which an anode, a cation separation
membrane (type: Nafion
®212), a cathode, and a gas diffusion layer are sequentially stacked, and which includes
an acid solution reservoir connected to the outside of the cathode and the membrane
electrode assembly and filled with an acidic solution (85%, H
3PO
4).
Reaction current density: 100 mA/cm2 (constant current operation)
Reaction voltage: 1 V to 4 V
Reaction temperature: 40 °C
Reaction pressure: 1 atm (atmospheric pressure)
Anode catalyst: IrO2 on Ti mesh
Cathode catalyst: Ag powder
Electrode area: 100 cm2
Gas diffusion layer: Sigracet 39BB
Anode electrolyte solution: 1.0 M CsHCO3 (25 ml/min)
Cathode reactant: 40 °C Humidified CO2 gas (200 ccm)
40 °C Humidified CO2 gas supply flow 200 ml/min
Example 2
[0039] A carbon dioxide electrolysis device was operated under the same conditions as in
Example 1, except that the reaction current density was 200 mA/cm
2.
Example 3
[0040] A carbon dioxide electrolysis device was operated under the same conditions as in
Example 1, except that the reaction current density was 300 mA/cm
2.
Comparative Example 1
[0041] A carbon dioxide electrolysis device was operated under the same conditions as in
Example 1, except that an anion exchange membrane was used instead of the cation exchange
membrane and an acid solution reservoir was not included.
Comparative Example 2
[0042] A carbon dioxide electrolysis device was operated under the same conditions as in
Example 2, except that an anion exchange membrane was used instead of the cation exchange
membrane and an acid solution reservoir was not included.
Comparative Example 3
[0043] A carbon dioxide electrolysis device was operated under the same conditions as in
Example 3, except that an anion exchange membrane was used instead of the cation exchange
membrane and an acid solution reservoir was not included.
Comparative Example 4
[0044] A carbon dioxide electrolysis device was operated under the same conditions as in
Example 1, except that an acid solution reservoir was not included.
Comparative Example 5
[0045] A carbon dioxide electrolysis device was operated under the same conditions as in
Example 2, except that an acid solution reservoir was not included.
Comparative Example 6
[0046] A carbon dioxide electrolysis device was operated under the same conditions as in
Example 3, except that an acid solution reservoir was not included.
Experimental Examples
[0047] A product resulting from a carbon dioxide reduction reaction performed through the
carbon dioxide electrolysis device according to each of Examples 1 to 3 and Comparative
Examples 1 to 6 was analyzed by gas chromatography. At this time, the amount of carbon
dioxide initially introduced was compared with the amount of produced carbon dioxide,
and the amount of carbon dioxide lost without being electrochemically reduced was
measured. In addition, Faraday efficiency was measured for carbon monoxide and hydrogen
according to the following measurement methods, and the measured properties are each
described in Table 1 below.
(1) Carbon dioxide loss rate (CO2 loss, %)
[0048] The gas composition at the discharge flow path was measured through Gas-Chromatography
(GC) analysis. The flow rate (mL/min) of a discharged gas was multiplied by the percentage
(%) of carbon dioxide measured through GC analysis, thereby measuring a flow rate
Q
CO2.f of discharged CO
2 after electrochemical conversion, which was compared with an initial input flow rate
Q
CO2.i to measure the total amount of CO
2 used (CO
2 used, %). Since the conversion ratio of CO during the CO
2 reduction reaction was 1:1, assuming that a flow rate Qco of a carbon monoxide gas
measured by GC analysis is equal to the amount (CO
2 conv, %) of electrochemically converted CO
2, the remainder obtained by subtracting the conversion amount from the amount of CO
2 used was calculated as CO
2 loss. The measured value was calculated through the following Equation 1.

(2) Carbon monoxide Faraday efficiency (%)
[0049] The gas composition at the discharge flow path was measured through Gas-Chromatography
(GC) analysis. In addition, Faraday efficiency was calculated through the following
equation.

[0050] In Equation 2 above, Q is a flow rate at a discharge flow path, F is a Faraday constant,
p is a pressure, T is a measurement temperature, and R is an ideal gas constant. A
total current i
total is a value of the total current applied over time, and a current i
product with respect to a product is a value calculated from a volume of gas V
product measured through GC analysis.
(3) Hydrogen Faraday efficiency (%)
[0051] The hydrogen Faraday efficiency was measured and calculated in the same way as the
above-described carbon monoxide Faraday efficiency (2).
[Table 1]
| Classificati on |
Current density (mA/cm2 ) |
Exchange membrane type/ whether acid solution reservoir is included (O/X) |
Hydroge n Faraday efficie ncy (%) |
Carbon monoxid e Faraday efficie ncy (%) |
Carbon dioxide loss rate (%) |
| Example 1 |
100 |
Cation exchange membrane/O |
0.80 |
100.15 |
4.72 |
| Example 2 |
200 |
Cation exchange membrane/O |
0.90 |
91.75 |
4.09 |
| Example 3 |
300 |
Cation exchange membrane/O |
3.31 |
84.10 |
4.41 |
| Comparative Example 1 |
100 |
Anion exchange membrane/X |
0.56 |
100.19 |
11.04 |
| Comparative Example 2 |
200 |
Anion exchange membrane/X |
0.67 |
95.39 |
20.46 |
| Comparative Example 3 |
300 |
Anion exchange membrane/X |
0.86 |
92.04 |
29.57 |
| Comparative Example 4 |
100 |
Cation exchange membrane/X |
2.85 |
100.19 |
14.01 |
| Comparative Example 5 |
200 |
Cation exchange membrane/X |
2.22 |
92.01 |
29.00 |
| Comparative Example 6 |
300 |
Cation exchange membrane/X |
6.31 |
81.33 |
41.37 |
[0052] Referring to Table 1, in the case of Examples 1 to 3 which include an acid solution
reservoir, compared to Comparative Examples 1 to 6 which do not include an acid solution
reservoir, the carbon monoxide Faraday efficiency remained at the same level, and
at the same time, the carbon dioxide loss rate was significantly low.
[0053] That is, the electrolysis device of the present invention separates carbon dioxide
again from a carbonate by including an acid solution reservoir, and thus, may significantly
reduce the loss of the carbon dioxide converted into the carbonate and have high electrolysis
efficiency. In contrast, in the case of Comparative Examples 1 to 3 which use an anion
exchange membrane or Comparative Examples 4 to 6 which use a cation exchange membrane
but do not include an acid solution reservoir, it can be seen that the amount of carbon
dioxide lost by being converted into a carbonate is large, so that the electrolysis
efficiency is degraded.
11: Anode
13: Cathode
15: Separation membrane
20: Acid solution reservoir
30: Discharge flow path
60: Gas-liquid separator
1. An electrolysis device comprising:
an electrolysis cell including a gas diffusion layer, a cathode, a separation membrane,
an anode, and an electrolyte solution; and
outside the electrolysis cell, an acid solution reservoir connected by a discharge
flow path for discharging a product from the cathode,
wherein the separation membrane is a cation separation membrane.
2. The electrolysis device of claim 1, wherein the acid solution reservoir comprises
an acidic solution containing one or more selected from the group consisting of phosphoric
acid, hydrochloric acid, sulfuric acid, nitric acid, acetic acid, citric acid, and
oxalic acid.
3. The electrolysis device of claim 1, wherein the electrolyte solution is an aqueous
solution containing one or more selected from the group consisting of Cs2CO3, CsHCO3, Cs2SO4, CsCl, CsNO3, K2CO3, KHCO3, K2SO4, K3PO4, KCl, KNO3, Na2CO3, NaHCO3, Na2SO4, Na3PO4, NaCl, and NaNO3.
4. The electrolysis device of claim 1, wherein the electrolysis cell is a zero-gap membrane
electrode assembly cell in which the gas diffusion layer, the cathode, the separation
membrane, and an anode with an anode liquid flow path formed therein are sequentially
stacked.
5. The electrolysis device of claim 1, wherein a product produced by an electrolysis
reaction in the cathode is transported to the acid solution reservoir through the
discharge flow path, wherein the product includes carbon monoxide, water vapor, and
a salt.
6. The electrolysis device of claim 5, wherein carbon dioxide produced from the salt
in the acid solution reservoir is supplied to the electrolysis cell.
7. The electrolysis device of claim 5, wherein the salt is a carbonate.
8. The electrolysis device of claim 1, wherein the electrolysis device electrolyzes carbon
dioxide.
9. The electrolysis device of claim 8, wherein the carbon dioxide is supplied in a state
including water vapor when supplied to the electrolysis cell.
10. The electrolysis device of claim 1, wherein the electrolysis device electrolyzes carbon
dioxide, thereby producing one or more selected from the group consisting of carbon
monoxide, ethylene, methane, formic acid, hydrocarbon, aldehyde, and alcohol.