ELECTROLYSER ARRANGEMENT

Abstract

An electrolyser arrangement with at least one electrolytic cell, having two electrodes, namely an anode and a cathode, each of the two electrodes being in contact with an electrode compartment for filling with a liquid electrolyte, the two electrode compartments being separated by a membrane and a conveying device being provided, one for each of the two electrodes, for conveying the electrolyte in each case in a circuit, a cathode circuit and an anode circuit, through the electrode compartment via at least one collection vessel per circuit and back into the electrode chamber. A device is provided outside the electrolytic cell, for conveying an auxiliary volume flow between the cathode circuit and the anode circuit.

Claims

1. An electrolyzer arrangement having comprising: at least one electrolysis cell comprising two electrodes, namely an anode and a cathode, wherein each of the two electrodes is in contact with an electrode space for filling with a liquid electrolyte, wherein the two electrode spaces are separated by a membrane, a conveyor apparatus for each of the two electrodes for conveying the electrolyte through the electrode space in a respective circuit, comprising a cathode circuit and an anode circuit, and an apparatus outside the electrolysis cell for conveying a secondary volume flow between the cathode circuit and the anode circuit.

2. The electrolyzer arrangement as claimed in claim 1, wherein the cathode circuit and the anode circuit each have a collecting container.

3. The electrolyzer arrangement as claimed in claim 2, wherein a first secondary volume flow takes place between a first collecting container and the second collecting container.

4. The electrolyzer arrangement as claimed in claim 1, further comprising: a second conveyor apparatus for producing a second secondary volume flow between the two circuits, which takes place in the opposite direction from the first secondary volume flow.

5. The electrolyzer arrangement as claimed in claim 4, wherein the second conveyor apparatus for producing the second secondary volume flow is configured in the form of a membrane module.

6. The electrolyzer arrangement as claimed in claim 5, wherein both the cathode circuit and the anode circuit pass through the membrane module.

7. The electrolyzer arrangement as claimed in claim 4, further comprising: a pump apparatus between the collecting containers in order to bring about the second secondary volume flow.

8. The electrolyzer arrangement as claimed in claim 2, further comprising: an overflow or a pump apparatus between the two collecting containers in order to bring about the first partial volume flow.

9. The electrolyzer arrangement as claimed in claim 1, wherein the membrane between the electrode spaces is a cation permeable membrane.

10. The electrolyzer arrangement as claimed in claim 8, wherein the secondary volume flow takes place from the cathode circuit to the anode circuit.

11. The electrolyzer arrangement as claimed in claim 1, further comprising: a vapor deposition container in the cathode circuit and/or in the anode circuit and there is provision for a connecting line from one of the vapor deposition containers to an educt supply apparatus.

12. A method for operating an electrolyzer having at least one electrolysis cell that in turn has two electrodes, comprising an anode and a cathode, wherein each electrode has an electrode space through which a liquid electrolyte having a conducting salt dissolved therein is conveyed in a respective conveyor circuit namely in a cathode circuit and an anode circuit, in a respective primary volume flow and wherein the two electrode spaces and hence the electrolyte contained therein are separated by a membrane, the method comprising: conveying the electrolyte from one circuit to a second circuit in a secondary volume flow.

13. The method as claimed in claim 12, wherein the secondary volume flow is at least 0.01 and at most 10% of the larger of the two primary volume flows.

14. The method as claimed in claim 13, wherein the secondary volume flow is at least 0.1 and at most 1% of the larger of the two primary volume flows.

15. The method as claimed in claim 12, further comprising: a collecting container in each of the two circuits; wherein the electrolyte in the secondary volume flow is conveyed from a first collecting container to a second collecting container.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0022] Further embodiments and further features of the invention emerge from the drawings. These are not a limitation for the invention, since they merely describe advantageous embodiments. In the drawings:

[0023] FIG. 1 shows an electrolyzer arrangement having a secondary volume flow between the anode circuit and the cathode circuit,

[0024] FIG. 2 shows an electrolyzer arrangement as in FIG. 1 having additional deposition containers,

[0025] FIG. 3 shows an electrolyzer arrangement having two options for depicting apparatuses for a secondary volume flow having two collecting containers,

[0026] FIG. 4 shows an electrolyzer arrangement having two options for depicting apparatuses for a secondary volume flow,

[0027] FIG. 5 shows a schematic depiction of an electrolyzer arrangement, wherein two collecting containers are in the foreground, and

[0028] FIG. 6 shows a membrane module.

DETAILED DESCRIPTION OF INVENTION

[0029] FIG. 1 schematically depicts an electrolyzer arrangement 2 that has an electrolysis cell 4 in which an electrolyte 5 is arranged. The electrolysis cell 4 has two electrodes, a cathode 7, which in this case is configured in the form of a gas permeable electrode, and an anode 6. The two electrodes, namely the anode 6 and the cathode 7, each adjoin an electrode space, a distinction being drawn between an electrode space 8 for the anode 6 and an electrode space 9 for the cathode 7. The two electrode spaces 8, 9 are separated from one another by a membrane 10. The electrode spaces contain the electrolyte 5, which, depending on where it is in the electrolysis cell 4, is referred to as anolyte 38, if it is in the electrode space 8 of the anode 6, and which is referred to as catholyte 40 if it is in the electrode space 9 of the cathode 7.

[0030] The electrolyte 5 or 38 and 40 is not in the electrode spaces 8 and 9 in a stationary manner, but rather is in a circuit 14, 15. To this end, there is provision for conveyor apparatuses 12 and 13, which each provide the applicable volume flow of electrolyte 5 or 38 and 40 for an anode circuit 14 or a cathode circuit 15. This involves the electrolyte 5 being moved along the respective circuit 14 (anode circuit) and 15 (cathode circuit). If the cathode circuit 15 is now considered in exemplary fashion, the catholyte 40 is pumped through the conveyor apparatus 13 from the electrode space 9 of the cathode 7 via the line provided with the reference sign 15.

[0031] Further, there exists in the electrolyzer arrangement an educt feed 42 that introduces an educt, for example carbon dioxide, into the electrolysis cell 4, and a product outlet 44. During the electrolysis, which involves electric current being applied to the cathode 7 and to the anode 6, the carbon dioxide is reduced in this example to carbon monoxide, which leaves the electrolysis cell 4 again via the product outlet 44. During this electrolysis, both protons and the cations of a conducting salt dissolved in the electrolyte 5, for example potassium, migrate through the membrane 10, which is in the form of a cation permeable membrane in this embodiment. This results in the anolyte 38 and the catholyte 40 having different concentrations of cations, in particular cations of the conducting salt, as electrolysis activity increases. This can be tolerated up to a certain degree of approximately 2% difference, the economic viability and profitability of the electrolysis process no longer being ensured upward of a specific concentration difference. For this reason, it is expedient to perform a constant exchange between the anolyte 38 and the catholyte 40. In accordance with the prior art, in an extremely simple form, a single collecting container is used that is part of both the circuit 14, the anode circuit, and the cathode circuit 15. In a common collecting container, which is not depicted here, good equalization of concentrations and complete mixing of the electrolyte 5 enriched or depleted in the electrolysis cell take place. However, product gases, in particular hydrogen in the cathode circuit 15 and oxygen from the anode circuit 14, are also transferred in this common collecting container, which is not depicted here. This can lead to an explosive mixture; additionally, product gases, such as carbon monoxide, which are likewise present in the common collecting container in small amounts, are contaminated by the gases oxygen and hydrogen.

[0032] To solve this problem, there is provision for a secondary volume flow 20 to take place, which takes place via a secondary volume flow apparatus 18. The secondary volume flow results in an exchange of concentrations taking place between the anode circuit and the cathode circuit, and vice-versa. The direction in which the secondary volume flow occurs is dependent on the respective process control. The secondary volume flow is advantageously no more than 10% of the electrolyte volume flows in the cathode circuit 15 or in the anode circuit 14. At minimum, the secondary volume flow is 0.01% of the electrolyte volume flow; in particular, the range that covers the secondary volume flow 20 is between 0.1% an 1% of the electrolyte volume flows. If the two electrolyte volume flows are of different magnitude, then the larger of the two electrolyte volume flows is used as reference for the secondary volume flow.

[0033] It is expedient in this instance for the pH value of the anolyte to be between 4 and 5 and for the pH value of the catholyte to be between 7 and 9 in steady-state operation.

[0034] FIG. 2 provides an analogous configuration of the apparatus shown in FIG. 1, there being provision in both the cathode circuit 15 and the anode circuit 14 for a respective deposition container 53, 55 in which respective gaseous constituents of the electrolyte can be removed. In the case of the deposition container 53, for example deposited carbon dioxide can be supplied to the educt supply apparatus 42 again.

[0035] In FIG. 3, there is provision for the cathode circuit 15 to have a collecting container 23 in which the catholyte 40 is conveyed and for the anode circuit 14 to have a collecting container 22 into which the anolyte 38 is put. The two collecting containers 23 and 22 are fundamentally separate from one another, and they likewise have, but in a different embodiment, an apparatus 18 that is used to produce a secondary volume flow 20. This apparatus 18 is depicted highly schematically in FIG. 3; it can be configured in the form of an overflow channel, for example, that allows a small amount to get from one container to the other collecting container by means of a defined gradient or a defined slope. It is also possible for an appropriate pipeline, not depicted here, or an appropriate hose to cause a secondary volume flow 20 between the containers 22 and 23, said flow being brought about by gravity or else by a pressure difference, for example.

[0036] FIG. 5 depicts an apparatus 18 for producing the secondary volume flow 20, said apparatus being provided in the form of pipelines that incorporate a pump 30. In this case, as shown in FIG. 5, it can also be expedient, in order to ensure equalization of concentrations between the anolyte 38 and the catholyte 40 in regard to the anions, for there to be provision for a second secondary volume flow 26 produced by a second conveyor apparatus 24, for example in the pump apparatus 30 shown in FIG. 5. In this case, it is also expedient for the two subcontainers 22, 23 to contain stirring apparatuses 27 that ensure uniform mixing of the electrolyte 38, 40 in the respective containers 22 and 23. It goes without saying that it is likewise possible to achieve good mixing inside the subcontainers without active stirring apparatuses, e.g. by means of a suitable flow guide.

[0037] If the membrane 10 used is a cation permeable membrane, a particularly large number of cations from the conducting salt migrate from the anode side, that is to say from the anolyte 38 that is in the electrode space 8 of the anode 6, through the membrane 10 to the electrode space 9 of the cathode 7. Together with the cations, water, what is known as drag water, also migrates through the membrane, so that equalization in particular from the cathode circuit 15 to the anode circuit 14 is necessary. In this case, when a cation permeable membrane is used, the first secondary volume flow from the cation circuit 15 to the anode circuit 14 therefore takes place. This advantageously takes place between the collecting container 23 of the cathode circuit 15 and the collecting container 22 of the anode circuit 14, specifically in the direction described. The second secondary volume flow is then used to equalize anions that ensue between the container 22 and the container 23 via the second secondary volume flow 26.

[0038] A further option for producing a secondary volume flow exists in the form of a membrane module 28 in which a membrane 29 is arranged (cf. FIGS. 3 and 4). Both the cathode circuit 15 and the anode circuit 14 pass through this membrane module 28 as shown in FIG. 3. In this case, the membrane module 28 has not only the membrane 29 but also two module chambers, a first module chamber 46 through which the anode circuit 14 runs and a second module chamber 47 through which the cathode circuit 15 goes. The module chamber 47 therefore contains the catholyte 40 and the module chamber 46 contains the anolyte 38. The membrane 29 in this case provides an exchange area for the dissolved ions in the electrolytes 38 and 40, specifically for cations and for anions. Porous membranes that are as thin as possible are particularly well suited to this task. These introduce a relatively low transport resistance, which means that comparatively small membrane areas are adequate. The transport in porous membranes (permeation) is caused by two different mechanisms, an externally enforced transport through pores, that is to say a purely convected transport, or a transport on the basis of diffusion of a dissolved component. The transport mechanism for the ions through the porous membrane corresponds to the diffusion, which takes place without energy consumption. What is known as the drag water can also be pushed through the membrane by convection, in principle, by applying a small differential pressure.

[0039] The necessary size of the porous membrane 29 can be ascertained by means of the maximum material flow rate of cations to be expected inside the electrolysis cell by at the same time stipulating a maximum tolerable concentration difference between the anolyte 38 and the catholyte 40 (for example 0.2 mol/l). With the aid of known passage coefficients, it is possible to estimate that when thin porous membranes 29 are used, the membrane module 28 can be configured to be distinctly smaller than the area provided therefor in the electrolysis cell 4 or the membrane 10 stretched therein. The entire membrane area of the membrane 29 is smaller than the entire electrolysis cell area of the membrane 10, but is at least one hundredth of the membrane area of the membrane 10. A ratio of from 1:20 between the membrane 29 and the membrane 10 to 1:5 between the membrane 29 and the membrane 10 is particularly advantageous.

[0040] The porous membrane 29 also allows water to be transported, in principle, by virtue of a lower differential pressure prevailing inside the membrane module 28. Said pressure is advantageously less than 100 mbar.

[0041] The entire arrangement described allows intermixing of the gases produced during the carbon dioxide electrolysis of the electrolysis cell 4 to be avoided, as a result of which complex conditioning of the electrolyte 5 or of the gases produced is dispensed with. By way of example, the catholyte 40 therefore contains no oxygen that contaminates the catholyte product gas. Additionally, neither product gas (for example carbon monoxide, methane or hydrogen) nor educt gas such as carbon dioxide is lost via the anolyte 38 in practice.

[0042] Use of two separate electrolysis circuits, namely the anode circuit 14 and the cathode circuit 15, cannot prevent a certain amount of drifting apart by the compositions and hence also by the pH values of the anolyte 38 and the catholyte 40. In addition, drag water from the anolyte 38 gets into the catholyte 40. Conventional conditioning would have a high level of associated energy expenditure, e.g. as a result of thermal degassing or vacuum degassing. Alternatively, the process can also have an additive added that chemically binds unwanted gases. The use of an additive has associated costs, however. In addition, it is not foreseeable to what extent possible additives influence the electrochemical process. The catalytic removal of undesirable gases likewise has a high level of associated energy expenditure. The arrangement described therefore shows a simple technical solution to ensure appropriate equalization of ions and water between the anode circuit 14 and the cathode circuit 15.