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    • 专利摘要:
    The invention essentially consists in proposing a new reactor architecture or fuel cell with an active section of the catalytic methanation or reforming reaction catalyst material integrated in the electrode that varies with the composition of the gases, as and when they occur. electrochemically dependent distribution on said electrode.
    公开号:FR3056338A1
    申请号:FR1658908
    申请日:2016-09-22
    公开日:2018-03-23
    发明作者:Magali REYTIER；Guilhem Roux；Jerome Laurencin；Michel Planque
    申请人:Commissariat a lEnergie Atomique CEA；Commissariat a lEnergie Atomique et aux Energies Alternatives CEA；
    IPC主号:
    专利说明:

    Holder (s): COMMISSIONER OF ATOMIC ENERGY AND ALTERNATIVE ENERGIES Public establishment.
    Extension request (s)
    Agent (s): NONY CABINET.
    PROCESSES FOR THE CO-ELECTROLYSIS OF WATER AND CO2 (SOEC) OR THE PRODUCTION OF HIGH TEMPERATURE ELECTRICITY (SOFC) PROMOTING OR NOT CATALYTIC REACTIONS WITHIN THE H2 ELECTRODE.
    FR 3 056 338 - A1 (6 // The invention essentially consists in proposing a new reactor or fuel cell architecture with an active section of the methanation or reforming reaction catalytic material integrated in the electrode which varies with the composition gases, as they are distributed depending on the electrochemistry on said electrode.
    Tl
    Exit
    Input E (H2) 1 S (H2) 2
    S (H2) 1
    PROCESSES FOR THE CO-ELECTROLYSIS OF WATER AND CO2 (SOEC) OR FOR THE PRODUCTION OF HIGH TEMPERATURE ELECTRICITY (SOFC) PROMOTING OR NOT CATALYTIC REACTIONS WITHIN THE H2 ELECTRODE
    Technical area
    The present invention relates to the field of solid oxide fuel cells (SOFC, acronym for "Solid Oxide Fuel Cell") and that of Telectrolysis of water at high temperature (EHT, or EVHT for electrolysis of water vapor). at high temperature, or HTE English acronym for "High Temperature Electrolysis", or HTSE English acronym for "High Temperature Steam Electrolysis") also with solid oxides (SOEC, English acronym for "Solid Oxide Electrolysis Cell").
    The invention relates more particularly to new methods of operating a high temperature co-electrolysis reactor (EHT) of SOEC type, from carbon dioxide CO2 and water vapor H2O to produce a gas of synthesis (mixture of CO and H2), or of a fuel cell of the SOFC type, with a stack of elementary electrochemical cells with solid oxides.
    It aims to propose a solution to favor or not the methanation reaction within an EHT reactor or the internal methane reforming reaction within a SOFC cell.
    Although described with reference mainly to the application of high temperature co-electrolysis of carbon dioxide CO2 and water H2O, the invention applies just as well to a SOFC fuel cell supplied with H2 and / or in methane CH4, as fuel and in Air or oxygen O2 as oxidizer.
    Prior art
    The electrolysis of water is an electrochemical reaction which decomposes water into dioxygen and dihydrogen gas with the help of an electric current according to the reaction:
    H 2 O ^ H 2 + U 0 2 .
    To carry out the electrolysis of water, it is advantageous to carry it out at high temperature, typically between 600 and 950 ° C., since part of the energy necessary for the reaction can be provided by heat which is less expensive than electricity and carrying out the reaction is more efficient at high temperature. To implement high-temperature electrolysis, it is known to use an electrolyser of the SOEC type (English acronym for “Solid Oxide Electrolysis Cell”), consisting of a stack of elementary patterns each comprising a solid oxide electrolysis cell. , consisting of three anode / electrolyte / cathode layers superimposed on each other, and interconnection plates, for example made of metal alloys, also called bipolar plates, or interconnectors. The interconnects have the function of ensuring both the passage of electric current and the circulation of gases in the vicinity of each cell (water vapor injected, hydrogen and oxygen extracted in an EHT electrolyser; air and hydrogen and / or methane injected and water extracted in an SOFC stack) and to separate the anode and cathode compartments which are the gas circulation compartments on the side of the anodes and cathodes respectively of the cells. To carry out the electrolysis of water vapor at high temperature EHT, water vapor H2O is injected into the cathode compartment. Under the effect of the current applied to the cell, the dissociation of water molecules in vapor form is carried out at the interface between the hydrogen electrode (cathode) and the electrolyte: this dissociation produces H2 hydrogen gas and oxygen ions. The dihydrogen is collected and evacuated at the outlet of the hydrogen compartment. The oxygen O 2 ions migrate through the electrolyte and recombine into oxygen at the interface between the electrolyte and the oxygen electrode (anode).
    As shown schematically in Figure 1, each elementary electrolysis cell 1 is formed of a cathode 2 and an anode 4, placed on either side of a solid electrolyte 3. The two electrodes (cathode and anode) 2 , 4 are conductors, made of porous material, and the electrolyte 3 is gas tight, electronic insulator and ionic conductor. The electrolyte can in particular be an anionic conductor, more precisely an anionic conductor of the O 2 and T electrolysers is then called anionic electrolysers.
    The electrochemical reactions take place at the interface between each of the electronic conductors and the ionic conductor.
    At cathode 2, the half-reaction is as follows:
    H 2 O + 4 e2 H 2 + 2 O 2 '.
    At anode 4, the half-reaction is as follows:
    O 2 -> O2 + 4th.
    The electrolyte 3 interposed between the two electrodes 2, 4 is the place of migration of the O 2 ′ ions under the effect of the electric field created by the potential difference imposed between the anode 4 and the cathode 2.
    As illustrated in brackets in FIG. 1, the water vapor entering the cathode can be accompanied by hydrogen H 2 and the hydrogen produced and recovered at the outlet can be accompanied by water vapor. Similarly, as illustrated in dotted lines, a draining gas, such as air can also be injected at the inlet to evacuate the oxygen produced. The injection of a draining gas has the additional function of playing the role of thermal regulator.
    An elementary electrolysis reactor consists of an elementary cell as described above, with a cathode 2, an electrolyte 3, and an anode 4 and two mono-pole connectors which provide the electrical, hydraulic and thermal.
    To increase the flow rates of hydrogen and oxygen produced, it is known to stack several elementary electrolysis cells one on top of the other, separating them by interconnection devices, usually called interconnectors or bipolar interconnection plates. The assembly is positioned between two end interconnection plates which support the electrical supplies and gas supplies of the electrolyser (electrolysis reactor).
    A high temperature water electrolysis reactor or electrolyzer (EHT) thus comprises at least one, generally a plurality of electrolysis cells stacked on top of each other, each elementary cell being formed of an electrolyte, of a cathode and an anode, the electrolyte being interposed between the anode and the cathode.
    Your fluidic and electrical interconnection devices which are electronic conductors, are in electrical contact with the electrodes and generally provide the functions of supply and collection of electric current and delimit one or more gas circulation compartments. More specifically, an interconnector ensures electrical contact by one of its faces with the cathode of a cell and by the other of its faces with the anode of the adjacent cell.
    Thus, a so-called cathode compartment has the function of distributing electric current and water vapor as well as recovering the hydrogen produced at the cathode in contact.
    A so-called anode compartment has the function of distributing the electric current as well as recovering the oxygen produced at the anode in contact, possibly using a draining gas.
    FIG. 2 represents an exploded view of elementary patterns of a high temperature water vapor coelectrolyzer according to the state of the art. This EHT co-electrolyser comprises a plurality of elementary co-electrolysis cells Cl, C2 ... of solid oxide type (SOEC) stacked alternately with interconnectors 5. Each cell Cl, C2 ... consists of a cathode 2.1, 2.2, ... and an anode 4.1, 4.2, between which an electrolyte is disposed 3.1, 3.2 .... All of the co-electrolysis cells are generally supplied in series by the electric current and in parallel by gases.
    The interconnector 5 is a metal alloy component which ensures the separation between the cathode 50 and anode 51 compartments, defined by the volumes comprised between the interconnector 5 and the adjacent cathode 2.1 and between the interconnector 5 and the adjacent anode 4.2 respectively. It also ensures the distribution of gases to the cells. The injection of a mixture of water vapor and carbon dioxide into each elementary unit takes place in the cathode compartment 50. The collection of the hydrogen and carbon monoxide produced and the residual water vapor at the cathode 2.1, 2.2 ... is carried out in the cathode compartment 50 downstream of the cell C1, C2 ... after dissociation of the water vapor and carbon dioxide by the latter. The oxygen produced at anode 4.2 is collected in the anode compartment 51 downstream of the cell C1, C2 ... after dissociation of the water vapor and carbon dioxide by the latter.
    The interconnector 5 ensures the passage of current between the cells C1 and C2 by direct contact with the adjacent electrodes, that is to say between the anode 4.2 and the cathode 2.1.
    In a SOFC solid oxide fuel cell according to the state of the art, the cells CI, C2 ... and interconnectors 5 used are the same components, but the operation is opposite to that of an EHT co-electrolyser such which has just been explained with a reverse current direction, with air which supplies the then cathode compartments 51 and hydrogen or methane as fuel which supplies the then anode compartments 50.
    Satisfactory operation of an EHT (co-) electrolyser or an SOFC fuel cell requires among others the following essential functions:
    A / good electrical insulation between two adjacent interconnectors in the stack, under penalty of short-circuiting the elementary electrochemical cell interposed between the two interconnectors,
    B / a good seal between the two separate compartments, i.e. anodic and cathodic, under penalty of recombination of the gases produced, leading to a reduction in yield and above all the appearance of hot spots damaging the stack,
    C / a good distribution of the gases both at the inlet and at the recovery of the gases produced, under penalty of loss of yield, inhomogeneity of pressure and temperature within the various elementary cells or even unacceptable inhibitions of the cells.
    In addition, the operating point selected for the electrolysis reactor or the SOFC cell also fixes the thermal conditions in the stack. Indeed, for electrolysis performed at high temperature, the AH energy necessary for the dissociation of the input molecule (H2O or CO2) can be provided in the form of electricity and / or heat. The thermal energy supplied Q is then defined as a function of the voltage U across the terminals of each electrolysis cell by the relation:
    Q = - H-UI,
    2F in which U is the electric voltage, I is the electric current and F is the Faraday constant.
    Thus, three operating regimes are defined for electrolysis or coelectrolysis, corresponding to three different thermal modes for stacking cells:
    - the so-called autothermal mode in which the imposed voltage Ui mp is equal to AH / 2F. The heat consumed by the dissociation reaction is completely compensated by the different electrical resistances of the electrolyser (irreversibilities). The electrolyser does not need any particular thermal management while remaining stable in temperature.
    - the so-called endothermic mode in which the imposed voltage Uimp is less than AH / 2F. The electrolyser consumes more heat than the electrical losses within it. This necessary heat must then be provided to it by another means, otherwise its temperature will drop irreparably.
    - the so-called exothermic mode in which the imposed voltage Uimp is greater than AH / 2F. The electrolysis then consumes less heat than the electrical losses by the Joule effect. This release of heat within the electrolyser must then be removed by another means, otherwise its temperature will rise prohibitively.
    The operation of a battery powered by CLL methane requires precautions. In fact, the thermal management of this type of cell is a compromise. On the one hand, the internal reforming reaction of the electrode supplied with CEL and water vapor, according to the equation CEL + ELO—> 3Eb + CO, catalyzed by the cermet, generally made of nickel-zirconia because the nickel has the advantage of being a very good catalyst for the above reforming reaction is highly endothermic, while the hydrogen oxidation reaction within the cell aimed at producing electricity is strongly exothermic .
    Thus, battery operation can also vary from an endothermic mode to an exothermic mode depending on the ratio between the internal reforming reaction and the current density. Without particular precautions, this requires managing strong thermal gradients in the stack, between the inlet and the outlet of the gases, these significant thermal gradients can be prohibitive because they induce strong mechanical stresses. In addition, the operation of a SOFC cell supplied only with pure hydrogen rapidly leads to a heating of the stack limiting the accessible powers and the efficiency, if high flow rates are used for cooling.
    In addition, the transportation, storage and use of the hydrogen or syngas produced requires minimal pressure. Rather than compressing the gas produced, which presents a significant cost, in particular for hydrogen, this type of electrolysis by SOEC can be done directly from pressurized steam, the water then being compressed with liquid state.
    The internal operation of a SOFC cell or an EHT reactor under pressure, typically from a few bars to a few tens of bars, typically 30 bars, then requires a solution to avoid loss of seals by the seals.
    A solution is already known which consists in placing the EHT stack reactor or SOFC stack within a sealed enclosure which is itself pressurized.
    We can cite here the patent applications or patents W02011 / 110674A1, US2002 / 0081471 and US 6689499 B2 which disclose this type of solution. This known solution offers the advantage of being able to impose the same pressure between the inside and the outside of the stack. This therefore allows operation at high pressure, from a few bars to a few tens of bars, without mechanical stress on the glass or glass ceramic seals.
    With this EHT reactor solution with pressure operation, it is possible to carry out the electrolysis of water vapor H2O to produce hydrogen on the one hand and oxygen on the other hand which can be upgraded independently . This same reactor can also allow the co-electrolysis of an H2O + CO2 mixture to form syngas, a mixture of H2 + CO in proportions dependent on the targeted fuel.
    In other words, it is possible and advantageous to envisage the production of a synthetic fuel gas by electrolysis of water vapor H2O to produce hydrogen H2 and / or the co-electrolysis of H2O + CO2 at high temperature. in a stack reactor of solid oxide cells in a pressure vessel.
    The electrolysis reactions of water vapor (I) and of co-electrolysis of H2O + CO2 (II) are carried out according to the following equations:
    Water electrolysis: H2O -ML + I / 2O2 (I)
    Co-electrolysis: CO2 + H2O CO + H2 + O2 (II).
    Thus, the electrolysis of water vapor H2O allows a fabrication of the combustible gas by injection of a mixture of hydrogen H2 produced according to the electrolysis (I) and carbon dioxide CO2 in a catalyst external to the electrolyser. .
    The co-electrolysis of H2O + CO2 also makes it possible to manufacture the combustible gas from synthesis gas (H2 + CO) produced according to the co-electrolysis (II).
    The combustible gas thus produced can be a hydrocarbon and in particular methane, the main component of natural gas.
    Different methods of obtaining a combustible gas by heterogeneous catalysis either directly from a mixture of H2 and carbon dioxide CO2, or indirectly from a synthesis gas (H2 + CO) have already been studied.
    In particular, the hydrogenation of CO2 to methane is an industrial process which has been studied at each energy shock, either to produce synthetic methane from pure CO2 and H2, or in coal gasification plants with gases and more complicated conditions (Fischer-Tropsch process).
    Each synthesis gas intended to produce a fuel requires a given H2 / CO ratio depending on the target fuel.
    Table 1 below thus illustrates the ratios required as a function of processes for the synthesis of different fuels:
    TABLE 1
    PROCESSSYNTHESIS PRODUCTCOMBUSTIBLEGOT CO-ELECTROLYSIS RATIO H 2 / CO NECESSARY STEAM ELECTROLYSIS H 2 O RATIO CO 2 / H 2 NECESSARY methane synthesis Natural gas 1/3 1/4 methanol synthesis Methanol 1/2 1/3 synthesis ofdimethyl ether (DME) DME 1/1 1/2 Ficher Tropsch synthesis Diesel 1/2 1/3
    For the methanation process, two ways are possible and have been more or less studied according to the state of the art.
    The first way is that of a single reaction according to the following equation:
    CO 2 + 4 // 2 CH, + 2H 2 O
    The second path is that of a two-step reaction according to the following equations:
    CO 2 + H2 ^ CO + H 2 O CO + 3H2 ^ CH, + H 2 O
    As highlighted by the authors of the publication [1] (see in particular Figures 3 and 4), the methanation reactions are favored at high pressure and at low temperature according to Le Chatelier's law. In fact, the thermodynamic calculations indicated in [1] indicate a theoretical conversion of 100% of CO 2 into CLL at less than 150 ° C against 83% at 400 ° C. However, it is also indicated that a minimum temperature and an optimum gas speed must be adjusted to guarantee sufficient kinetics.
    The catalysts used for methanation are generally based on nickel supported by a zirconium oxide (ZrO 2 ), or based on nickel (Ni) supported by an aluminum oxide (AI2O3).
    An electrode commonly used in EHT (co-) electrolysis reactors or SOFC fuel cell is based on nickel, such as a nickel and yttria zirconia cermet denoted Ni-YSZ. Nickel in particular has the advantage of also being a very good catalyst for the reforming of methane and / or its formation by hydrogenation of CO 2 and CO.
    From these publications, the inventors therefore concluded that it was possible to produce methane directly within a co-electrolysis reactor, as a function of the temperature, pressure and flow rate of the gases.
    However, these methanation reactions are exothermic. Thus, just as for the reforming reaction of a SOFC cell supplied with CFL methane, the heat balance of a pressurized co-electrolysis reactor used to carry out methanation, must take into account the exothermicity of this reaction .
    Thus, the electrochemical reactions necessary for the operation of this type of stack in a (co-) electrolysis reactor or SOFC fuel cell can be carried out under various electrical, thermal and catalytic conditions, each having its own advantages and disadvantages.
    In particular, in endothermic mode for electrolysis, less electricity is consumed but less hydrogen is produced and heat must be supplied to the stack. The advantage of this operating point lies in the availability of an inexpensive heat source. It all depends on the nature, the temperature of this heat source and the design of the interconnector to make the most of this heat.
    Conversely, the exothermic mode for electrolysis as for the cell leads to a significant production either of the gases formed or of electricity, but the stack must be cooled either by the gases, which can be difficult to perform and costly energy , either by catalytic reactions involving the input species or formed by the reactions.
    An important constraint is to best manage these thermal operating regimes of a fuel cell (SOFC) or an electrolyzer (EHT).
    In addition, whatever interconnector design adopted to date in a solid oxide cell stack reactor which can operate under pressure either as a (co-) electrolysis reactor or as a SOFC fuel cell , it is not possible to favor or not, as desired, the catalytic reactions within the reactor ίο without degrading the electrochemical functioning, because the catalytic and electrochemical surfaces are the same and correspond to the surface of the cermet.
    There is therefore a need to improve the electrolysis or coelectrolysis reactors and the SOFC fuel cells with stack of solid oxide cells operating at high temperature, in particular in order to be able to favor or not, as desired, the catalytic reactions liable to occur. within them, more particularly the methanation reaction or the methane reforming reaction without impacting the electrochemical functioning.
    An object of the invention is to meet this need at least in part.
    Statement of the invention
    To do this, the invention relates, under a first alternative, to a process of co-electrolysis of EEO water vapor and carbon dioxide CO2 and, where appropriate, of methanation, implemented in a reactor comprising a stack of elementary electrolysis cells of solid oxide type, of rectangular or square surface, each formed by a cathode comprising methanation reaction catalyst material (s), an anode and an electrolyte interposed between the cathode and anode, a plurality of electrical and fluidic interconnectors each arranged between two adjacent elementary cells with one of its faces in electrical contact with the anode of one of the two elementary cells and the other of its faces in electrical contact with the cathode of the other of the two elementary cells, and a plurality of electrical contact and gas distribution elements, each arranged between a cathode and an interconnector.
    In the process according to the invention:
    - a first zone and a second zone of each interconnector are supplied independently, with a mixture of EEO water vapor and carbon dioxide CO2 (EH2 (1) and EH2 (2)), and it is distributed to the cathode of each elementary cell, then the synthesis gas produced (mixture of carbon monoxide CO and hydrogen EE) and, where appropriate, the mixture of EEC methane and additional EEO water vapor produced by methanation, is recovered within of the cathode, in a third zone and a fourth zone of each interconnector (SH2 (1) and (SH2 (2)) in fluid communication with the first zone and the second zone respectively, each electrical contact and gas distribution element integrating a sealing bead forming a gas distribution barrier separating a first gas flow sector (Tl) comprising the first and third zones, from a second gas flow sector (T2) comprising the second and fourth zones, the first era and second sectors being joined by the barrier by forming a surface substantially equal to that of each cell; the first to fourth zones being dimensioned and the gas circulation barrier being arranged so that the gas flow section is increasing or decreasing between the first and third zones within the first sector and the gas flow section is also increasing or decreasing between the second and fourth zones within the second sector;
    - the first and second zones of each interconnector are supplied so that the circulation at each cathode in the first flow sector (Tl) is against the flow of the circulation in the second flow sector (T2).
    According to an advantageous embodiment, the flow sectors are generally trapezoidal.
    It is specified here that the increasing shape, in particular trapezoidal of the sectors is obviously to be considered in top view of the stack. And that the cell surface is the active one considered when viewed from above.
    According to a variant, the catalytic surface is supplied by the largest base of the first and second trapezoidal sectors defined respectively by the first and the third zones, in order to minimize the methanation reaction compared to the coelectrolysis reaction within the stack. decreasing along the path of gases produced for the same electrochemical surface
    Alternatively, the catalytic surface is supplied by the smallest base of the first and second trapezoidal sectors defined respectively by the first and the third zones, in order to maximize the methanation reaction compared to the co-electrolysis reaction within the stack. increasing along the path of gases produced for the same electrochemical surface. This makes it possible to envisage manufacturing in situ, at least in part, the water necessary for co-electrolysis by this methanation reaction rather than by vaporization.
    Advantageously, the length ratio between small and large bases of the trapezoidal sectors is determined beforehand in order to favor or not the methanation reaction compared to the co-electrolysis reaction within the stack.
    According to an advantageous embodiment, a fifth zone of each interconnector (E (O2)) is supplied with draining gas, such as air, and it is distributed to the anode of each cell, then the oxygen is recovered. O2 produces and, where appropriate, the draining gas in a sixth zone of each interconnector S (O2), so as to have a supply of draining gas and a recovery of produced oxygen common to the first and second trapezoidal sectors.
    Advantageously, the co-electrolysis is carried out at least in part with the water vapor H2O produced by methanation.
    The invention also relates, under a second alternative, to a process for producing electricity at high temperature, implemented in a solid oxide fuel cell (SOFC) comprising a stack of elementary electrochemical cells of the SOFC type, each formed of a cathode, an anode comprising methane reforming reaction (CTL) material (s), and an electrolyte interposed between the cathode and the anode, a plurality of electrical and fluidic interconnectors arranged each between two adjacent elementary cells with one of its faces in electrical contact with the anode of one of the two elementary cells and the other of its faces in electrical contact with the cathode of the other of the two elementary cells, and a plurality electrical contact and gas distribution elements, each arranged between an anode and an interconnector.
    In the process according to the invention:
    - a fuel is supplied independently to a first zone and a second zone of each interconnector, and it is distributed to the anode of each elementary cell then the surplus of fuel is recovered (CLL and, where appropriate, mixture of monoxide of carbon CO and hydrogen LL following reforming) and the water produced, in a third zone and a fourth zone of each interconnector in fluid communication with the first zone and the second zone respectively; each electrical contact and gas distribution element incorporating a sealing bead forming a gas distribution barrier separating a first gas flow sector (Tl) comprising the first and third zones, from a second flow sector gases (T2) comprising the second and fourth zones, the first and second sectors being joined by the barrier, forming a surface substantially equal to that of each cell; the first to fourth zones being dimensioned and the gas circulation barrier being arranged so that the gas flow section is increasing or decreasing between the first and third zones within the first sector and the gas flow section is also increasing or decreasing between the second and fourth zones within the second sector;
    - the first and second zones of each interconnector are supplied in such a way that the circulation at each anode in the first flow sector is counter-current to the circulation in the second flow sector.
    The gas barrier separates the electrical contact element into two separate flow sectors, and also the porous H2 electrode. It can be a glass, glass-ceramic bead or a solder which advantageously infiltrates the electrode during its installation. The barrier thus has the function of obstructing the passage of gases without the need for perfect sealing. Realizing the barrier according to the invention from a glass ceramic bead is particularly advantageous. A glass ceramic comes at room temperature in the form of a paste which is easy to penetrate a porous metallic substrate, such as a nickel grid and also the porous H2 electrode. A rise in temperature of the joint at temperatures between 850 and 1000 ° C. will allow the glass-ceramic to melt, which will be set up hot and follow the shape of the porous substrate of the electrical contact element by filling the porosities, such than the mesh of the nickel grid, and this according to the continuous barrier profile that one wishes to give it. Once in place, the barrier is crystallized at the operating temperatures of the reactor or the fuel cell, typically between 600 and 850 ° C., and therefore prevents any passage of the injected gases (H2O, H2, CO, CO2, CH4,. ..) from a flow sector Tl to the other T2 which is joined to it.
    According to a variant, the largest base of the first and second trapezoidal sectors delimited by the first and the third zone is supplied, in order to maximize the reforming reaction compared to the production of water within the stack by oxidation. hydrogen.
    Alternatively, it is supplied by the smallest base of the first and second trapezoidal sectors bounded respectively by the first and the third zone, in order to minimize the reforming reaction compared to the production of water within the stack, which allows to consider making in situ, at least in part, the water necessary for reforming.
    Advantageously, the length ratio between small and large bases of the trapezoidal sectors is determined beforehand in order to favor or not the reforming reaction compared to the reaction for producing water by oxidation of hydrogen within the stack.
    According to an advantageous embodiment, a fifth zone of each interconnector is supplied with oxidant, such as air, and it is distributed to the cathode of each cell, then the surplus of oxidant remaining in a sixth zone is recovered. each interconnector, so as to have a supply of oxidizing gas and an oxygen recovery remaining common to the first and second trapezoidal sectors.
    The fuel can advantageously be hydrogen or methane (CLL), or a mixture of the two.
    Advantageously, the reforming is carried out at least in part with the water produced by oxidation.
    Preferably, the first and second trapezoidal sectors are supplied with identical gas compositions and flow rates in nominal operation. Conversely, in the event of the need to further heat or cool one of the sectors of the stack compared to the other, it can be envisaged not to supply each sector in an identical manner.
    This need may arise in the event of a malfunction (leak, heating enclosure in which the defective stack is placed, thermal insulation problem): in this case, not supplying a sector compared to the other joint allows more or more heating cool one with respect to the other joined sector.
    Thus, the invention essentially consists in proposing a new reactor or fuel cell architecture with an active section of the methanation or reforming catalytic reaction material integrated in the electrode which varies with the composition of the gases, as and when their distribution depending on the electrochemistry on said electrode.
    This variation in the active catalytic section encountered by the gases along their distribution is carried out without modifying the electrochemical surface of the cells and therefore of the collection or supply of the current which remains identical to the state of the art.
    This variation in catalytic section is achieved by dividing the supply and recovery of the gases into two independent circuits within each interconnector and by physically separating the gas flow surface on the electrode (and catalyst) at by means of a barrier integrated into each electrical contact element, as well as within the electrode, which define two contiguous trapezoidal flow sectors whose sum of their surface is that square or rectangular of the electrochemical surface of the cells.
    Thus, for the same electrochemical surface, the reactions to the electrodes comprising catalytic material (s) (cathodes in a co-electrolysis reactor or anodes in a fuel cell) can be favored or not depending on the evolution of the velocity of the gases distributed determined by the location of the large bases of the trapezoids either at the inlet of the gases, or at the outlet of the products resulting from the electrochemical reaction.
    Thanks to the invention, a decoupling is carried out within the same stack between electrochemical reaction and catalytic activity, which makes it possible in part to better manage the species produced along the gas flow, but above all to manage the thermal of the stack by controlling the catalytic reaction without changing the electrochemical operating point.
    Thus, in fuel cell mode, it is preferable to maximize the rapid internal reforming so that the oxidation of hydrogen can take place quickly, otherwise the cells will be damaged.
    In the co-electrolysis mode of H2O + CO2, depending on the use of synthesis gas (H2 + CO) envisaged at the outlet of the reactor, which must be converted into methane or other products, we can seek to promote methanation in located within the reactor or, on the contrary, seek to avoid it.
    In other words, by introducing a variation in catalytic section between the input and the output of the electrode, the invention makes it possible to decouple the catalytic reaction of methanation or reforming from that of electrochemistry which takes place within the stack. of the reactor or of the SOFC stack respectively.
    And by determining beforehand, the dimensional relationships between the catalytic inlet section and the outlet section, we can define as desired a precise and determined ratio between catalytic reaction and electrochemical reaction.
    In addition, a subsequent advantage of the invention is the possibility of reducing the amount of water to be vaporized at the inlet of the co-electrolysis reactor, thanks to the methanation reaction which can be promoted in situ. Indeed, a methanation reaction also forms water.
    Therefore, the fact of favoring the implementation of methanation within a co-electrolysis reactor makes it possible to obtain water in situ already in the vapor form and therefore to already have part of the water. necessary for co-electrolysis without the need to vaporize this quantity of liquid water upstream.
    This can have a considerable impact on the performance of a global installation, in particular because having water already in the vapor form makes it possible to avoid vaporizing by a separate electrical source, in the absence of an external hot source and therefore makes it possible to reduce the energy costs of operating the installation, and thereby obtain better efficiency.
    In addition, the new architecture according to the invention has the advantage of improving the overall thermal uniformity of each cell in the case of electrochemical or catalytic reactions generally exothermic or endothermic.
    In fact, the thermal sources which appear at a precise location in the cell (typically either at the inlet or at the outlet), can create thermal gradients which can be prohibitive in terms of the mechanical strength of this cell.
    Thanks to the invention, the thermal gradients are greatly reduced along the cell, since each of these edges comprises both an inlet and an outlet (first and third area, as well as second and fourth area). The temperature differences within each cell are then reduced thanks to the design of the sectors within the stack.
    The interconnectors envisaged in the context of the invention make it possible to maintain a circulation of gases on the cross-current cells between the fuel and the oxidant or draining gas.
    The methods according to the invention do not modify the reversibility of a stack of this type which can be used both as a SOEC co-electrolysis reactor with optionally in situ methanation, and as a SOFC cell with as hydrogen, and / or methane with internal reforming.
    The subject of the invention is also, according to the first alternative, a SOEC co-electrolysis reactor for the implementation of a co-electrolysis of the water vapor LEO and of carbon dioxide CO2 and, where appropriate, of an in situ methanation reaction comprising a stack of elementary electrolysis cells of the solid oxide type, of rectangular or square surface, each formed by a cathode comprising methanation reaction catalyst material (s), an anode and an electrolyte interposed between the cathode and the anode, a plurality of electrical and fluidic interconnectors each arranged between two adjacent elementary cells with one of its faces in electrical contact with the anode of one of the two elementary cells and the other of its faces in electrical contact with the cathode of the other of the two elementary cells, and a plurality of electrical contact and gas distribution elements, each arranged between a cathode and an interconnector, cha that electrical contact and gas distribution element integrating a sealing bead forming a gas distribution barrier separating a first gas flow sector (Tl) comprising the first and third zones, from a second flow sector gases (T2) comprising the second and fourth zones, the first and second sectors being joined by the barrier, forming a surface substantially equal to that of each cell; the first to fourth zones being dimensioned and the gas circulation barrier being arranged so that the gas flow section is increasing or decreasing between the first and third zones within the first sector (Tl) and the section gas flow is also increasing or decreasing between the second and fourth zones within the second sector (T2).
    The invention also relates, according to the second alternative, to a high temperature fuel cell (SOFC) for the possible implementation of an internal methane reforming (CEE), comprising a stack of elementary cells of the oxide type. solids, of rectangular or square surface, each formed of a cathode, an anode comprising material (s) catalyst (s) of the methane reforming reaction (CEE), and an electrolyte interposed between the cathode and the anode, a plurality of electrical and fluidic interconnectors each arranged between two adjacent elementary cells with one of its faces in electrical contact with the anode of one of the two elementary cells and the other of its faces in electrical contact with the cathode of the other of the two elementary cells, and a plurality of electrical contact and gas distribution elements, each arranged between a cathode and an interconnector, each electrical contact and distribution element gas separating a first gas flow sector (Tl) comprising the first and third zones, from a second gas flow sector (T2) comprising the second and fourth zones, the first and second sectors being joined by the barrier by forming an area substantially equal to that of each cell; the first to fourth zones being dimensioned and the gas circulation barrier being arranged so that the gas flow section is increasing or decreasing between the first and third zones within the first sector (Tl) and the section gas flow is also decreasing or increasing between the second and fourth zones within the second sector (T2).
    In the context of the invention, each interconnector is advantageously a part consisting of three flat sheets, elongated along two axes of symmetry X, Y orthogonal to one another, one of the end sheets being intended to come into mechanical contact with the plane of a cathode of an elementary electrochemical cell and the other of the end plates being intended to come into mechanical contact with the plane of an anode of an adjacent elementary electrochemical cell, in which:
    - one of the end sheets, called the first end sheet, has a pierced central part while the other of the end sheets, called the second end sheet, as well as the central sheet has a non-pierced central part,
    each of the three flat sheets has a central part, pierced at its periphery with six slots, the first to fourth slots of each sheet being elongated over a length corresponding to part of the length of the central section along one of the axes X sheets and being distributed two by two on either side of said axis X, while the fifth and sixth lumen are each elongated over a length corresponding substantially to the length of the central part along the other of the axes Y,
    - The first end plate further comprises a seventh and an eighth lumens arranged symmetrically on either side of the Y axis, inside its first to fourth lumens, and are elongated over a length corresponding substantially to the length of the central part along the Y axis, while the other of the end sheets, called the second end sheet, further includes a seventh, eighth, ninth and tenth lights respectively inside its first , second third and fourth lights, each of these seventh to tenth lights being elongated over a length corresponding substantially respectively to the length of the first to fourth lights along the axis X, and,
    - the first to sixth lumens of the central plate are widened inwards relative to the first to sixth lumens of each end plate respectively,
    - The first and second lights of the three sheets are of dimensions that are substantially identical to each other and the third and fourth lights of the three sheets are of dimensions that are substantially identical to each other, the length of the first and second lights is preferably greater than that of the third and fourth lights ,
    - The seventh and eighth lights of the second end sheet are of dimensions substantially identical to those of its first and second lights, while the ninth and tenth lights of the second end sheet are of dimensions substantially identical to those of its third and fourth lights,
    - all the enlarged openings of the central sheet have in their enlarged part, tabs of sheets spaced from each other by forming a comb, each of the slots defined between the edge of a widened slot and a tab or between two consecutive tabs emerging on one of the interior lights respectively of the first or of the second end sheet, the three sheets are laminated and assembled together such that:
    The sheet metal tabs form spacers between the first and second end sheets respectively between the fifth and seventh lights of the first end sheet, between the sixth and eighth lights of the first end sheet, between the first and seventh lights of the second end sheet, between the second and eighth lights of the second end sheet, between the third and ninth lights of the second end sheet, and between the fourth and tenth lights of the second end sheet, • each of the first to sixth lights of one of the three sheets is in fluid communication individually respectively with one of the first to sixth corresponding lights of the other two sheets, • the fifth and seventh lights of the first end plate are in fluid communication through the slots of the enlarged fifth lumen of the central plate, while the sixth and eighth lumen es of the first end sheet are in fluid communication through the slots of the sixth enlarged lumen of the central sheet, • the first and seventh lights of the second end sheet are in fluid communication through the slots of the first enlarged lumen of the central plate, while the second and eighth lumens of the second end plate are in fluid communication through the slots of the enlarged second lumen of the central plate, the third and the ninth lumens of the second end sheet are in fluid communication through the slots of the third enlarged lumen of the central sheet, and the fourth and tenth lights of the second end sheet are in fluid communication through the slots of the fourth enlarged light of the central sheet.
    Advantageously, the reactor and the SOFC cell constitute the same device intended to operate reversibly in co-electrolysis mode, if necessary with in situ methanation and in fuel cell mode, if necessary with internal methane reforming.
    Preferably, the cathodes comprising methanation reaction catalyst material (s) or the anodes comprising methane reforming reaction (CEE) catalyst material (s), each preferably being based on nickel (Ni) supported by zirconia (ZrCE), such as a nickel and yttria zirconia cermet denoted Ni-YSZ.
    According to an advantageous alternative embodiment, each electrical contact and gas distribution element is a nickel (Ni) grid integrating, as a sealing barrier, a glass-based or glass-ceramic-based bead.
    Preferably, this barrier also penetrates the porous electrode (cathode for the EHT reactor, anode for cell), such as a Ni-YSZ cermet electrode. This creates a complete seal between the two adjoining sectors of the same circulation compartment.
    In summary, the methods and electrolyser / fuel cell according to the invention have many characteristics and advantages, among which we can cite:
    a physical separation of the electrochemical surface of the same cell into two sectors of trapezoidal shape (in front view of the cell) contiguous and independent, the trapezoidal shape defining a section of catalytic material which varies gradually with the composition of the gases along the flow in this section;
    - the physical separation is carried out by integrating a gas tightness barrier within the electrical contact and gas distribution element, as well as within the porous Hz circulation electrode. Preferably, the barrier is a glass or glass-ceramic bead integrated in a nickel grid, the glass or the glass-ceramic penetrating both the grid and the electrode;
    - Control of the preponderance or not of catalytic reactions compared to electrochemical reactions, and this by determining beforehand the geometry of the two trapezoidal sectors, in particular the length ratio between small and large base of each trapezoid. With the entry of gases through the large base of the sectors, the catalytic section decreases and the gas speed increases along their distribution on each cell, which reduces the catalytic reactions involved along the electrochemical distribution. Conversely, with the entry of gases through the small base of the sectors, the catalytic section increases and the speed of the gas decreases along their distribution on each cell, which makes it possible to favor the catalytic reactions involving the gases produced by electrochemistry along distribution;
    - an improvement in the thermal homogeneity of the cells of the stack compared to those of an EHT reactor or SOFC cell electrolysis at high temperature according to the state of the art;
    - possible management of the methane obtained in a high temperature coelectrolysis reactor and preferably operating under pressure, preferably between 5 and 30 bars;
    - possible management of the synthesis gas obtained within an SOFC cell by internal reforming, thus conditioning the thermal of the cell;
    -a possible management of the water vapor formed within a SOEC stack of co-electrolysis by promoting the methanation reaction in situ, which saves part of the energy of vaporization of water required upstream of the stack and thereby allows a gain in the efficiency of an installation comprising the co-electrolysis reactor according to the invention.
    By “support cathode cell” is meant here and within the framework of the invention the definition already given in the field of electrolysis of water at high temperature EHT and designated under the acronym CSC for “Cathode- supported cell ”, ie a cell in which the electrolyte and the oxygen electrode (anode) are placed on the thicker hydrogen or carbon monoxide electrode (cathode) which therefore serves as a support.
    By “reversible” is meant in the context of the invention that the SOFC fuel cell can be used as a SOEC electrolyser in the electrolysis operating mode, opposite to that of the cell, T (les) anode ( s) of the SOFC cell then playing the role of cathode (s) of the electrolyser.
    detailed description
    Other advantages and characteristics of the invention will emerge more clearly on reading the detailed description of examples of implementation of the invention made by way of illustration and not limitation, with reference to the following figures among which:
    Figure 1 is a schematic view showing the principle of operation of a high temperature water electrolyser;
    FIG. 2 is a diagrammatic exploded view of part of a high temperature steam coelectrolyser comprising interconnectors according to the state of the art, FIG. 3 is a diagrammatic sectional view of a reactor of electrolysis using the high temperature co-electrolysis process according to a mode of the invention, FIG. 4 is a schematic view from above of a co-electrolysis reactor implementing the high temperature co-electrolysis process according to a mode of the invention, FIG. 5 is a schematic view from above of a coelectrolysis reactor implementing the high temperature coelectrolysis method according to another mode of the invention, alternative to that of FIG. 4 , FIG. 6A is an exploded view from below of a part of a co-electrolysis reactor according to the invention with interconnectors and an element for electrical contact and distribution of gases allowing independent supply and circulation of gases catho diques (HzO, CO2, H2, CO, CH4) against the current, from a trapezoidal sector to another joint whose sum of surfaces is equal to that of a co-electrolysis cell, Figure 6B is an exploded view from above of the reactor part shown in FIG. 6A, the supply / recovery of the draining gas and of the oxygen produced, being common to the two trapezoidal sectors, FIG. 7 is an exploded view of an interconnector a coelectrolysis reactor according to an embodiment of the invention, which allows an independent supply and circulation of cathode gases (H2O, CO2, H2, CO, CH4), from a sector of trapezoidal shape to another joint whose the sum of the surfaces is equal to that of a co-electrolysis cell, FIG. 7A is a detailed view of FIG. 7, FIG. 7B is a detailed perspective view of FIG. 7, FIGS. 8A and 8B are front views respectively on either side of an interconnector of a salt co-electrolysis reactor the invention showing more precisely the arrangement of the sealing cords, the barrier delimiting the trapezoidal sectors in accordance with the invention, as well as the path of the gases, the circulation of the oxygen produced taking place in a single compartment over all the surface of the anode;
    FIGS. 9A and 9B correspond respectively to FIGS. 8A and 8B by showing more precisely the arrangement of the weld lines of the three flat sheets forming an interconnector according to the invention, FIGS. 10A and 10B are front views respectively from side and side. another of an interconnector of a co-electrolysis reactor according to the invention showing more precisely the arrangement of the sealing beads, the barrier delimiting the trapezoidal sectors in accordance with the invention, as well as the path of the gases with the circulation of the oxygen produced taking place in two distinct trapezoidal sectors.
    It is specified here that in all of FIGS. 1 to 10B, the symbols and arrows for supplying a portion of water vapor H2O and carbon dioxide CO2, for distributing and recovering the products of co- electrolysis with the methanation reaction in situ where appropriate, and oxygen O2 and current are shown for clarity and precision, to illustrate the operation of a water vapor co-electrolysis reactor and of CO2 according to the state of the art and of a water vapor co-electrolysis reactor according to the invention.
    It is also specified that throughout the application the terms "above", below "," plumb "," vertical "," lower "," upper "," bottom "," top "," below " and "above" are to be understood by reference with respect to an SOEC electrolysis reactor or an SOFC cell in vertical configuration in operation, that is to say with the interconnectors and electrochemical cells planes horizontally, l 'electrode 02 below the electrode H2. Finally, it is specified that all the electrolysers described are of the solid oxide type (SOEC, English acronym for “Solid Oxide Electrolysis Cell”) operating at high temperature. The high operating temperature of an electrolyser (electrolysis reactor) is typically between
    600 ° C and 950 ° C.
    Typically, the characteristics of a SOEC elementary electrolysis cell suitable for the invention, of the cathode (H2 electrode) support (CSC) type, can be those indicated as follows in table 2 below.
    TABLE 2
    Electrolysis cell Unit Value Cathode 2 Constituent material Ni-YSZ Thickness pm 315 Thermal conductivity WnfK 4 13.1 Electrical conductivity Ω 1 m 1 10 5 Porosity 0.37 Permeability m 2 10 13 Tortuosity 4 Current density A.m ' 2 5300 Anode 4 Constituent material LSM Thickness pm 20 Thermal conductivity WnfK 4 9.6 Electrical conductivity Ω 1 m 1 1 10 4 Porosity 0.37 Permeability m 2 10 13 Tortuosity 4 Current density Am 2 2000
    Electrolyte 3 Constituent material YSZ Thickness pm 90pm in support electrolyte and5 pm in support electrode Resistivity Ω m 0.42
    Typically, the surface of a cell is of the order of 100 cm 2 .
    Figures 1 and 2 have already been described in detail in the preamble. They are therefore not described below.
    By convention, and in order to facilitate the reading of the gas flows in the different figures, the following symbols are used:
    - EH2 (1): designates the entry of gases flowing through T stack of the mixture of water vapor and carbon dioxide supplying a trapezoidal sector Tl of the co-electrolysis cells Cl, C2 ...;
    - SH2 (1): designates the outlet of the gases flowing through the stack and containing the products of the co-electrolysis reaction and, where appropriate, methanation in situ, recovered at the outlet of a trapezoidal sector Tl to the co cells -electrolysis Cl, C2. ;
    -EH2 (2): designates the entry of gases flowing through the stack of the mixture of water vapor and carbon dioxide supplying a trapezoidal sector T2 of the co-electrolysis cells Cl, C2 ...;
    -SH2 (2): designates the outlet of the gases circulating through the stack and containing the products of the co-electrolysis reaction and, where appropriate, of methanation in situ, recovered at the outlet of a trapezoidal sector T2 to the co cells -electrolysis Cl, C2;
    -E (C> 2): designates the entry of the oxidizing gas flowing through T stack and supplying all the co-electrolysis cells Cl, C2;
    -S (C> 2): designates the outlet of the oxidizing gas circulating through the stack and containing the oxygen produced at the co-electrolysis cells Cl, C2 ...
    The inventors were able to analyze that it was possible to produce methane directly within a co-electrolysis reactor, according to the typical temperature and pressure conditions.
    On the strength of the observation, the inventors have also highlighted that despite the numerous developments in the architecture of reactors with a stack of solid oxide cells and more particularly of the interconnectors, it is not possible or not to favor, as desired, catalytic reactions within existing reactors, regardless of the electrochemical operation, since the catalytic and electrochemical surfaces are the same and correspond to the surface of the cermet.
    Also, to overcome this difficulty, they thought of defining a reactor with a catalytic section of the cathode which varies with the composition of the gases along the distribution. They then thought of dividing the active cathode surface into two contiguous trapezoidal sectors whose sum of surfaces corresponds to the total surface of an electrochemical cell and in which the circulation of gases in one of the sectors is against the current of the other.
    Thus, for the same electrochemical surface of the cell (the sum of the two trapezoids) the methanation catalytic reaction may or may not be favored by the evolution of the gas speed within these sectors, as well as by the catalytic section traversed by a mixture of gases given along the path on the cell. The prior determination of the shape of the trapezoids, in particular the length ratio of their bases makes it possible to control this ratio between methanation reaction and electrochemical coelectrolysis reaction.
    The process of co-electrolysis of LLO water vapor and carbon dioxide CO2 and, where appropriate, in situ methanation, according to the invention is implemented in a reactor 1 comprising a stack of elementary electrolysis cells C 'l, C2 ... of solid oxide type, rectangular or square surface.
    Each cell C1, C2 ... is formed of a cathode 2.1, 2.2 ... comprising methanation reaction catalyst material (s), an anode 4.1, 4.2 ... and an electrolyte 3.1, 3.2 ... inserted between the cathode and the anode.
    The stack further comprises a plurality of electrical and fluidic interconnectors 5 each arranged between two elementary cells C1, C2 adjacent with one of its faces in electrical contact with the anode 4.1 of a C1 of the two elementary cells and the other of its faces in electrical contact with the cathode 2.2 of the other C2 of the two elementary cells, and a plurality of elements 9 of electrical contact and of gas distribution, each arranged between a cathode and an interconnector.
    According to the invention, each element 9 of electrical contact and gas distribution integrating a sealing bead 10, as shown diagrammatically in FIGS. 4 and 5. Preferably, to produce these cords, a glass or glass-ceramic bead is deposited on each of the nickel grids which will both penetrate the nickel grid and the porous cathode and thus make a sealed separation between the two adjoining sectors T1, T2 of the cathode compartments.
    In addition, as illustrated in FIGS. 3 to 5, a first zone (input EH2 (1) on the left in FIG. 3 and above in FIG. 4) and a second zone (input EH2 (2) are independently supplied. right in FIG. 3 and below in FIG. 4) of each interconnector 5, in a mixture of water vapor H2O and carbon dioxide CO2 and it is distributed to the cathode 2.1, 2.2 of each elementary cell C1, C2 ... then recovering, the synthesis gas produced (mixture of carbon monoxide CO and hydrogen H 2 ) and if necessary the mixture of methane CH4 and additional water vapor H2O produced by methanation in a third zone (outlet SH2 (1) at the bottom in FIG. 4) and a fourth zone (outlet SH2 (2) at the top in FIG. 4) of each interconnector in fluid communication respectively with the first zone and the second zone, the bead of sealing 10 forming a gas distribution barrier 10 separating the first trapezoidal sector (Tl) comprising l es first and third zones, of a second trapezoidal sector (T2) comprising the second and fourth zones, the first and second sectors being joined by the barrier by forming a surface substantially equal to that of each cell; the first to fourth zones being dimensioned and the gas circulation barrier being arranged so that the gas flow section is increasing or decreasing between the first and third zones within the sector (Tl) and the flow section gas is also increasing or decreasing between the second and fourth zones within the second sector (T2).
    All the first to fourth zones of the interconnectors 5 are located individually vertically in line with the first to fourth zones of the other interconnectors 5 of the stack, respectively.
    In addition, as visible in FIGS. 4 and 5, the first and second zones of each interconnector are supplied in such a way that the circulation at each cathode in the first trapezoidal sector T1 is counter-current to the circulation in the second trapezoidal sector T2 .
    In the configuration according to FIG. 4, the mixture of water vapor and carbon dioxide is supplied by the largest base of the trapezoidal sectors Tl and T2, in order to minimize the methanation reaction in situ compared to the reaction of co3056338 electrolysis at within the stack, the catalytic surface decreasing along the path of the gases produced for the same electrochemical surface.
    In the configuration according to FIG. 5, the mixture of water vapor and carbon dioxide is supplied by the smallest base of the trapezoidal sectors Tl and T2, in order to maximize the methanation reaction compared to the coelectrolysis reaction within l stack, the catalytic surface increasing along the path of the gases produced for the same electrochemical surface
    The interconnectors 5 can also be made to arrange the different supply and recovery zones for the draining gas and the oxygen produced so that their circulation at the level of the cells C1 is co-current with that at the level of the cells C2 or against the current.
    FIGS. 6A and 6B show schematically a part of a high temperature solid oxide co-electrolyser (SOEC) according to the invention.
    This co-electrolysis reactor comprises a stack of elementary SOEC type electrolysis cells (Cl, C2) each formed by a cathode 2.1, 2.2, an anode 4.1, 4.2 and an electrolyte 3.1, 3.2, interposed between the cathode and the anode.
    An electrical and fluidic interconnector 5 is arranged between two adjacent elementary cells C1, C2 with one of its faces in electrical contact with the anode of one of the two elementary cells and the other of its faces in electrical contact with the cathode of the other of the two elementary cells.
    As shown in FIGS. 6A and 6B, provision is also made for insulation and sealing frames 11 making it possible to provide electrical insulation between two adjacent interconnectors 5. Each frame 11 is pierced with lights O adapted to accommodate tie rods for fixing the stack, as well as seals 12 provided for sealing around the gas supply lights in co-electrolysis H2O, CO2, Air and recovery of the gases produced LL, CO, O2 with Air, as well as around the cell.
    All of the electrolysis cells Cl and C2 are crossed by the same electric current.
    In the reactor according to the invention, all the cathode compartments 50 of cells C1, C2 of the same trapezoidal sector T1 or T2 in which circulate the mixture of water vapor H2O and supply CO2 and the hydrogen produced LL with possibly syngas communicate with each other. On the other hand, the circulation of gases inside each cathode compartment 50 of the trapezoidal sector T1 is independent of that of the sector T2.
    The co-electrolysis reaction produces oxygen which is collected by all the anode compartments 51 which communicate with each other.
    According to the invention, each element 9 of electrical contact and gas distribution integrating a sealing bead 10 forms a gas distribution barrier between on the one hand a first 61, 71, 81 and a third 63, 73, 83 interconnector zone 5 and on the other hand between a second 62, 72, 82 and a fourth 64, 74, 84 interconnector zone.
    The first to fourth interconnector zones 5 are dimensioned and the gas circulation barrier 10 is arranged such that the distribution of the gases between the first 61,71,81 and the third 63, 73, 83 zone is carried out in a first sector Tl of trapezoidal shape. The gas distribution between the second 62, 72, 82 and the fourth zone 64, 74, 84 is carried out in a second sector T2 of trapezoidal shape.
    As visible in FIG. 6B, the two trapezoidal sectors T1 and T2 are joined by the barrier 10 by forming a surface substantially equal to that rectangular or square of each cell.
    In addition, as shown in FIGS. 8A and 8B, a seal 12 provides sealing at the periphery of the cathode compartment 50. The barrier 10 is also contiguous with this seal 12.
    FIG. 7 shows an exploded view of an interconnector 5 according to the invention making it possible to supply water vapor H2O and Co2, circulation against the current in the two trapezoidal sectors of the mixture of water vapor, of CO2 , and syngas produced in cells C1, C2 as well as the recovery of oxygen O2 produced within the stack.
    The interconnector 5 consists of three flat sheets 6, 7, 8 elongated along two axes of symmetry (X, Y) orthogonal to each other, the flat sheets being laminated and assembled together by welding. A central sheet 7 is interposed between a first 6 and a second 8 end sheet.
    The second 8 end sheet is intended to come into mechanical contact with the plane of a cathode 2.1 of a cell C1 of elementary electrolysis and the central sheet 7 is intended to come into mechanical contact with the plane of an anode 4.1 of an adjacent elementary electrolysis cell, each of the two adjacent elementary electrolysis cells (Cl, C2) of SOEC type being formed by a cathode 2.1, 2.2, an anode 4.1, 4.2 and an electrolyte 3.1, 3.2 interposed between the cathode and the anode.
    Each of the three flat sheets 6, 7, 8 has a central part 60, 70, 80.
    The first end plate 6 has a pierced central part 60 while the second end plate 8, as well as the central plate 7 has an undrilled central part 80 and 70 respectively.
    Each sheet 6, 7, 8 is pierced, at the periphery of its central part, with six slots 61, 62, 63, 64, 65, 66; 71, 72, 73, 74, 75, 76; 81, 82, 83, 84, 85, 86.
    The first 61, 71, 81 to fourth 64, 74, 84 slots of each sheet are elongated over a length corresponding to a part of the length of the central part 60, 70, 80 along one of the axes X of the sheets and are distributed two by two on either side of said axis X.
    The fifth 65, 75, 85 light is elongated over a length corresponding substantially to the length of the central part 60, 70, 80 along the other of the Y axes.
    The sixth 66, 76, 86 lumen is elongated over a length substantially corresponding to the length of the central part 60, 70, 80 along the other of the Y axes.
    The first 6 end plate further comprises a seventh 67 and eighth 68 lights arranged symmetrically on either side of the Y axis, inside its first to fourth lights 61 to 64, and are elongated on a length corresponding substantially to the length of the central part along the Y axis.
    The second 8 end plate further comprises a seventh 87, eighth 88, ninth 89 and tenth 800 lights respectively inside its first 81, second 82, third 83 and fourth 84 lights, each of these seventh to tenth lights being elongated over a length corresponding substantially respectively to the length of the first to fourth lumens along the axis X.
    As visible in FIG. 7, the first 71 to sixth 76 lumens of the central sheet are widened inwards relative to the first 61, 81 to sixth 66, 86 lumens of each end sheet 6, 8 respectively.
    The first 61, 71, 71 and second 62, 72, 82 slots of the three sheets 6, 7, 8 are substantially of dimensions which are substantially identical to one another.
    The third 63, 73, 83 and fourth 64, 74, 84 slots of the three sheets 6, 7, 8 are of dimensions which are substantially identical to one another.
    The length of the first 61, 71, 71 and second 62, 72, 82 lights is greater than that of the third 63, 73, 83 and fourth 64, 74, 84 lights of the three sheets 6, 7, 8. The length ratio between that first and second lights and that of the third and fourth light determines the geometric shape of the trapezoidal sectors Tl, T2 and therefore determines the ratio that can be obtained between the methanation reaction in situ and the electrochemical co-electrolysis reaction.
    The seventh 87 and eighth 88 lights of the second end sheet 8 are of dimensions substantially identical to those of its first 81 and second 82 lights.
    The ninth 89 and tenth 800 lights of the second end plate 8 are of dimensions in the X direction substantially identical to those of its third 83 and fourth 84 lights.
    All the openings 71 to 76 of the central sheet 7 have in their enlarged part, tabs of sheets spaced from each other by forming a comb, each of the slots defined between the edge of an enlarged slot and a tab or between two consecutive tabs opening onto one of the interior lights 67, 68 or 87, 88, 89, 800 respectively of the first 6 or of the second 8 end plate.
    The stratification and assembly of the three sheets 6, 7, 8 therebetween are carried out such that:
    • the sheet metal tabs form spacers between first and second 8 end sheets respectively between the fifth 65 and seventh 67 lights of the first end sheet 6, between the sixth 66 and eighth 68 lights of the first sheet end 6, between the first 81 and seventh 87 lights of the second 8 end sheet, between the second 82 and eighth 88 lights of the second 8 end sheet, between the third 83 and ninth 89 lights of the second end sheet, and between the fourth 84 and tenth 800 lights of the second 8 end sheet, • each of the first 71 to sixth 76 lights of the central sheet 7 is in fluid communication individually with Tune of the first 61.81 respectively at the sixth 66, 86 corresponding lights of the two other sheets 6, 8, • the fifth 65 and the seventh 67 lights of the first end sheet 6 are in fluid communication through the slots of the fifth light ière 75 enlarged of the central sheet 7, while the sixth 66 and the eighth 68 lights of the first end sheet are in fluid communication through the slots of the sixth light 76 enlarged of the central sheet 7, • the first 81 and the seventh 87 lights of the second end sheet 8 are in fluid communication through the slots of the first light 71 enlarged of the central sheet 7, while the second 82 and the eighth 88 lights of the second sheet d end 8 are in fluid communication through the slots of the second enlarged second light 72 of the central sheet 7, the third 83 and the ninth 89 lights of the second end sheet are in fluid communication through the slots of the third enlarged lumen 73 of the central sheet 7, and the fourth 84 and the tenth 800 lumens of the second end plate 8 are in fluid communication through the slots of the fourth lumen 74 enlarged of the central sheet trale 7.
    FIGS. 7A and 7B show in detail the embodiment of the comb formed by the sheet metal tabs 710 at the level of the enlarged slot 71 of the central sheet and its arrangement between the two end sheets 6, 8 in order to allow the supply of 'a cell, here a mixture of H2O water vapor and carbon dioxide CO2. Thus, the comb formed 710, 711 allows the mixture to pass from the supply clarinet 61, 71, 81 to the distribution slot 87 passing in the space between the two end sheets 6, 8. The thickness of the central plate 7 at the level of this comb 710, 711 gives it a spacer function and thus guarantees the height of the passage for the gas mixture in the inter-plate end space 6, 8. Such a passage of the gas according to the invention through the interior of the interconnector 5a for the advantage of freeing up a flat surface for making the seals. In addition, thanks to these comb shapes for the widened slots 71.72, on the one hand and 75 on the other hand, a homogeneous distribution of each gas (LEO, CO2, Air) is obtained over each trapezoidal sector of a cell. co-electrolysis, and thanks to these comb shapes for the enlarged slots on the one hand 73, 74 and 76 on the other hand recovery of the gases produced (LE, CO, O2).
    We will now describe with reference to FIGS. 8A and 8B, the operating method of a co-electrolysis reactor according to the invention as it has just been described:
    The first 61, 71, 81 lights are supplied with a mixture of water vapor and carbon dioxide CO 2 from the interconnector 5 (see note EH2 (1)) and simultaneously but separately the second 62, 72, 82 lights of the same interconnector 5 also with, preferably, the same mixture and the same flow rate (see note EH2 (2)).
    The path within an interconnector 5 of the injected gas mixture gradually transforming into TT + CO is shown diagrammatically in FIGS. 8A. It can be seen that each trapezoidal sector T1 is traversed by the counter-current mixture of the one which traverses the contiguous trapezoidal sector T2. The barrier 10 within the electrical contact element 9 and the electrode 2.1, preferably a nickel grid and the peripheral seal, preferably made of glass, allow a perfect seal between on the one hand the two sectors T1 and T2 and vis-à-vis the outside of the stack on the other hand.
    In addition, the fifth 65, 75, 85 lights of the three sheets 6, 7, 8 of each interconnector 5 are supplied with a draining gas (mention E (O 2 )), such as air or pure oxygen. .
    The path of the air as a injected draining gas and of the oxygen produced within an interconnector 5 is shown diagrammatically in FIG. 8B.
    The hydrogen and the CO produced (s) (SH2 (1)) are thus recovered by the coelectrolysis of water vapor and CO2 as well as, if necessary, the methane produced by the methanation reaction within of the electrode 2.1 at the sector Tl of the cells, in the third 63, 73, 83 slots of each interconnector 5.
    The hydrogen and the CO produced (s) (also SH2 (2)) are also recovered by the co-electrolysis of water vapor and CO2 as well as, if necessary, the methane produced by the methanation reaction with level of the sector T2 of the cells, in the fourth 64, 74, 84 lights of each interconnector 5.
    Simultaneously, the oxygen O2 product S (O 2 ) is recovered in the sixth 66, 76, 86 lumens of the three sheets 8 of each interconnector 5. The circulation of draining gas and the recovery of oxygen are therefore common to all the cells, independently of their separation into two sectors T1, T2 at the cathodes.
    FIGS. 10A and 10B show a variant of gas circulation on the side of the anode 4, according to which the same separation is made in two contiguous trapezoidal sectors on the side of the oxygen electrode (anode 4). As can be seen, the trapezoidal sectors on the side of cathode 2 are 90 ° from those on the side of anode 4. Thus, the draining gas such as air supplies the zone 66.1, 76.1, 86.1 and independently the zone 65.2, 75.2, 85.2. And the oxygen produced with, if necessary, the draining gas is recovered in zone 65.1, 75.1, 85.1 and independently in zone 66.2, 76.2, 86.2. The circulation of the oxygen produced between zone 66.1, 76.1, 86.1 and the zone
    65.1, 75.1, 85.1 is also against the current between zone 65.2, 75.2, 85.2 and zone
    66.2, 76.2, 86.2.
    This results in a cross-flow circulation of the oxygen produced relative to the hydrogen produced with also a circulation of the oxygen produced in two distinct trapezoidal sectors.
    The three flat sheets 6, 7, 8 constituting each interconnector 5 according to the invention are thin flat metal sheets, drilled and assembled together by welding. Preferably, the thin sheets are sheets with a thickness of less than 3 mm, typically of the order of 0.2 mm. All the welds between sheets are made during manufacture, and can advantageously be carried out using a laser technique by transparency, which is possible due to the thin thickness of the thin sheets, typically of the order of 0.2 mm.
    All the sheets are advantageously made of ferritic steel with around 20% chromium, preferably made of CROFER® 22APU or FT18TNb, AISI 441, or based on Nickel of the Inconel® 600 or Haynes® type in thicknesses typically between 0.1 and 1 mm.
    The assembly by weld lines ls around the openings between flat sheets 6, 7, 8 guarantees a good seal during the operation of the electrolyser between the mixture of water vapor and carbon dioxide CO2 brought to the interconnectors 5 and distributed. as well as the gases recovered in a trapezoidal sector Tl and that in the adjoining sector T2, and with the draining gas supplied E (O2) and the oxygen S (O2) recovered. The weld lines are illustrated in FIGS. 9A to 9B.
    As illustrated in all of FIGS. 7 to 10B, the three sheets 6, 7, 8 are pierced at their periphery with additional openings O adapted to accommodate fixing tie rods. These tie rods make it possible to apply a holding force to the stack of the various components of the electrolysis reactor.
    The invention is not limited to the examples which have just been described; one can in particular combine together characteristics of the examples illustrated within variants not illustrated.
    Other variants and improvements can be envisaged in the context of the invention.
    In particular, if the material inserted into the nickel grid 8 and into the cathode 2 to make the sealing bead 10 is a glass ceramic in the examples detailed above, it may be any material which prevents the passage of gases and can be easily shaped within a porous metallic substrate of a contact element.
    It can especially be a solder, before or after it is mounted in the stack.
    Reference cited [1]: Fabien Ocampo et al, “Méthanation of carbon dioxide over nickel-based Ce0.72Zr0.28O2 mixed oxide catalystsprepared by sol-gel method”, Journal of Applied Catalysis A: General 369 (2009) 90-96;
    权利要求:
    Claims (22)
    [1" id="c-fr-0001]
    1. Process for the co-electrolysis of water vapor H2O and carbon dioxide CO2 and, where appropriate, methanation in situ, implemented in a reactor (1) comprising a stack of elementary electrolysis cells (Cl, C2) of solid oxide type, of rectangular or square surface, each formed by a cathode (2.1, 2.2) comprising methanation reaction catalyst material (s), an anode (4.1, 4.2) and an electrolyte (3.1, 3.2) interposed between the cathode and the anode, a plurality of electrical and fluidic interconnectors (5) each arranged between two elementary cells (Cl, C2) adjacent with one of its faces in electrical contact with the anode (4.1) of one (Cl) of the two elementary cells and the other of its faces in electrical contact with the cathode (2.2) of the other (C2) of the two elementary cells, and a plurality of elements (9) electrical contact and gas distribution, each arranged between a cathode and an interconnector, according to which:
    - a first zone (61, 71, 81) and a second zone (62, 72, 82) of each interconnector (5) are supplied independently (EH2 (1); EH2 (2)) with a mixture of water vapor H2O and carbon dioxide CO2 and it is distributed to the cathode of each elementary cell then we recover (SH2 (1); SH2 (2)), the synthesis gas produced (mixture of carbon monoxide CO and hydrogen EE) and if necessary the mixture of CEE methane and additional EEO water vapor produced by methanation, within the cathode itself, in a third zone (63, 73, 83) and a fourth zone (64 , 74, 84) of each interconnector in fluid communication with the first zone and the second zone respectively; each element (9) for electrical contact and gas distribution integrating a sealing bead (10) forming a gas distribution barrier separating a first gas flow sector (Tl) comprising the first and third zones, a second gas flow sector (T2) comprising the second and fourth zones, the first and second sectors being joined by the barrier, forming a surface substantially equal to that of each cell; the first to fourth zones being dimensioned and the gas circulation barrier being arranged so that the gas flow section is increasing or decreasing between the first and third zones within the first sector (Tl) and the section gas flow is also increasing or decreasing between the second and fourth zones within the second sector (T2);
    - the first and second zones of each interconnector are supplied so that the circulation at each cathode in the first flow sector (Tl) is against the flow of the circulation in the second flow sector (T2).
    [2" id="c-fr-0002]
    2. Method according to claim 1, the flow sectors being of trapezoidal shape.
    [3" id="c-fr-0003]
    3. Method according to claim 2, according to which the largest base of the first and second trapezoidal sectors delimited by the first and third zones is supplied, in order to minimize the in-situ methanation reaction compared to the co-reaction. electrolysis within the stack.
    [4" id="c-fr-0004]
    4. Method according to claim 2, according to which one feeds by the smallest base of the first and second trapezoidal sectors delimited by the first and the third zone respectively, in order to maximize the in-situ methanation reaction compared to the co-reaction. electrolysis within the stack.
    [5" id="c-fr-0005]
    5. Method according to any one of claims 2 to 4, according to which the length ratio between small and large bases of the trapezoidal sectors is determined beforehand in order to favor or not the methanation reaction compared to the co-electrolysis reaction. within the stack.
    [6" id="c-fr-0006]
    6. Method according to any one of the preceding claims, according to which a fifth zone (65, 75, 85) of each interconnector is supplied with draining gas, such as air, (El (02)) or pure oxygen. 5), and it is distributed to the anode of each cell, then the oxygen O2 produced and, where appropriate, the draining gas (S 1 (02)) are recovered in a sixth zone (66, 76, 86) of each interconnector, so as to have a draining gas supply and a recovery of product oxygen common to the first and second flow sectors.
    [7" id="c-fr-0007]
    7. Method according to any one of the preceding claims, according to which the co-electrolysis is carried out at least in part with the water vapor H2O produced by methanation.
    [8" id="c-fr-0008]
    8. Process for the production of electricity at high temperature with internal methane reforming (CEE) if necessary, implemented in a solid oxide fuel cell (SOFC) comprising a stack of elementary electrochemical cells (Cl, C2) of SOFC type, each formed of a cathode (2.1, 2.2), an anode (4.1, 4.2) comprising material (s) of methane reforming reaction catalyst (CEE), and an electrolyte ( 3.1, 3.2) inserted between the cathode and the anode, a plurality of electrical and fluidic interconnectors (5.1; 5.2) each arranged between two adjacent elementary cells (Cl, C2) with one of its faces in electrical contact with the anode (4.1) of one (Cl) of the two elementary cells and the other of its faces in electrical contact with the cathode (2.2) of the other of the two elementary cells (C2), and a plurality of electrical contact elements and gas distribution, each arranged between an anode and an interconnector, according to which:
    - one supplies (EH2 (1); EH2 (2)), independently a first zone (61, 71, 81) and a second zone (62, 72, 82) of each interconnector (5), with a fuel, and it is distributed to the anode of each elementary cell, then the surplus fuel (CH2 (1); SH2 (2)) is recovered (CH4 and, if appropriate, mixture of carbon monoxide CO and hydrogen FF following reforming ) and the water produced, in a third zone (63, 73, 83) and a fourth zone (64, 74, 84) of each interconnector in fluid communication with the first zone and the second zone respectively; each electrical contact and gas distribution element separating a first gas flow sector (Tl) comprising the first and third zones, from a second gas flow sector (T2) comprising the second and fourth zones, the first and second sectors being joined by the barrier, forming a surface substantially equal to that of each cell; the first to fourth zones being dimensioned and the gas circulation barrier being arranged so that the gas flow section is increasing or decreasing between the first and third zones within the first sector (Tl) and the section gas flow is also increasing or decreasing between the second and fourth zones within the second sector (T2);
    - the first and second zones of each interconnector are supplied so that the circulation at each anode in the first flow sector (Tl) is against the flow of the circulation in the second flow sector (T2).
    [9" id="c-fr-0009]
    9. A method of producing high temperature electricity according to claim 8, the flow sectors being of trapezoidal shape.
    [10" id="c-fr-0010]
    10. A method of producing electricity at high temperature according to claim 9, according to which the largest base of the first and second trapezoidal sectors delimited by the first and third zones is supplied, in order to maximize the reforming reaction compared to the oxidation of hydrogen to water within the stack.
    [11" id="c-fr-0011]
    11. A method of producing electricity at high temperature according to claim 9, according to which the smallest base of the first and second trapezoidal sectors delimited by the first and the third zone is supplied, in order to minimize the reforming reaction compared to the oxidation of hydrogen to water within the stack.
    [12" id="c-fr-0012]
    12. A method of producing electricity at high temperature according to any one of claims 9 to 11, according to which the length ratio between small and large bases of the trapezoidal sectors is determined beforehand in order to favor or not the reaction of the reforming reaction compared to the oxidation reaction of hydrogen to water within the stack.
    [13" id="c-fr-0013]
    13. A method of producing electricity at high temperature according to any one of claims 8 to 12, according to which a fifth zone (65, 75, is fed (E1 (O2)) by oxidizing, such as air. 85) from each interconnector (5), and it is distributed to the cathode of each cell, then the surplus of oxidizer not consumed is recovered (S 1 (02)) in a sixth zone (66, 76, 86) of each interconnector , so as to have a supply and recovery of oxidizing gas common to the first and second flow sectors.
    [14" id="c-fr-0014]
    14. A method of producing electricity at high temperature according to one of claims 8 to 13, the fuel being hydrogen or methane (CEE) mixed with water vapor H2O, or a mixture of hydrogen and of CO, or a mixture of each of these gases.
    [15" id="c-fr-0015]
    15. A method of producing electricity at high temperature according to one of claims 8 to 14, according to which the reforming is carried out at least in part with the water produced by oxidation.
    [16" id="c-fr-0016]
    16. Method according to any one of the preceding claims, according to which the first and second flow sectors are supplied with identical gas compositions and flow rates in nominal operation.
    [17" id="c-fr-0017]
    17. SOEC co-electrolysis reactor for carrying out a co-electrolysis of EEO water vapor and carbon dioxide CO2 and, where appropriate, an in-situ methanation reaction comprising a stack of cells elementary electrolysis (Cl, C2) of solid oxide type, of rectangular or square surface, each formed by a cathode (2.1, 2.2) comprising methanation reaction catalyst material (s), an anode ( 4.1, 4.2) and an electrolyte (3.1, 3.2) interposed between the cathode and the anode, a plurality of electrical and fluidic interconnectors (5.1; 5.2) each arranged between two adjacent elementary cells (Cl, C2) with a of its faces in electrical contact with the anode (4.1) of one (Cl) of the two elementary cells and the other of its faces in electrical contact with the cathode (2.2) of the other (C2) of the two elementary cells , and a plurality of electrical contact and gas distribution elements (9), each arranged between a cathode and a n interconnector, each electrical contact and gas distribution element incorporating a sealing bead (10) forming a gas distribution barrier separating a first gas flow sector (Tl) comprising the first (61, 71, 81 ) and third (63, 73, 83) zones, of a second gas flow sector (T2) comprising the second (62, 72, 82) and fourth (64, 74, 84) zones, the first and second sectors being joined by the barrier forming a surface substantially equal to that of each cell; the first to fourth zones being dimensioned and the gas circulation barrier being arranged so that the gas flow section is increasing or decreasing between the first and third zones within the first sector (Tl) and the section gas flow is also increasing or decreasing between the second and fourth zones within the second sector (T2).
    [18" id="c-fr-0018]
    18. High temperature fuel cell (SOFC) for the possible implementation of an internal methane reforming (CH4), comprising a stack of elementary electrolysis cells (Cl, C2) of solid oxide type, surface rectangular or square, each formed by a cathode (2.1, 2.2), an anode (4.1, 4.2) comprising methane reforming reaction (CEE) catalyst material (s), and an electrolyte (3.1, 3.2) interposed between the cathode and the anode, a plurality of electrical and fluidic interconnectors (5.1; 5.2) each arranged between two adjacent elementary cells (Cl, C2) with one of its faces in electrical contact with the anode (2.1) of one (Cl) of the two elementary cells and the other of its faces in electrical contact with the cathode (4.2) of the other (C2) of the two elementary cells, and a plurality of contact elements (9) electrical and gas distribution, each arranged between an anode and an interconnector, each contact element metric and gas distribution integrating a sealing bead (10) forming a gas distribution barrier separating a first gas flow sector (Tl) comprising the first (61, 71, 81) and third (63, 73 , 83) zones, of a second gas flow sector (T2) comprising the second (62, 72, 82) and fourth (64, 74, 84) zones, the first and second sectors being joined by the barrier in forming an area substantially equal to that of each cell; the first to fourth zones being dimensioned and the gas circulation barrier being arranged so that the gas flow section is increasing or decreasing between the first and third zones within the first sector (Tl) and the section gas flow is also increasing or decreasing between the second and fourth zones within the second sector (T2).
    [19" id="c-fr-0019]
    19. Reactor according to claim 17 and fuel cell according to claim 18, constituting the same device intended to operate reversibly in co-electrolysis mode, if necessary with methanation in situ and in fuel cell mode, if necessary with internal methane reforming.
    [20" id="c-fr-0020]
    20. Reactor or fuel cell according to one of claims 17 to 19, the cathodes comprising material (s) of methanation reaction catalyst or the anodes comprising material (s) of reforming reaction catalyst (s) methane (CH4), each being based on nickel (Ni) supported by zirconia (ZrCk), such as a nickel and yttria zirconia cermet denoted Ni-YSZ.
    [21" id="c-fr-0021]
    21. Reactor or fuel cell according to one of claims 17 to 20, each element (9) of electrical contact and gas distribution being a nickel (Ni) grid integrating, as a sealing barrier, a bead (10) glass-based or glass-ceramic based.
    [22" id="c-fr-0022]
    22. Reactor or fuel cell according to claim 21, the cord (10) further separating the porous electrode (cathode for the EHT reactor, anode for cell).
    1/7 elementary
    2/7 γ> C2> C3
    Exit
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    同族专利:
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    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    JPS6463271A|1987-09-02|1989-03-09|Hitachi Ltd|Fuel cell|
    JP2006114387A|2004-10-15|2006-04-27|Toyota Motor Corp|Fuel cell|
    JP2007265939A|2006-03-30|2007-10-11|Ngk Insulators Ltd|Electrochemical device|
    JP2009026524A|2007-07-18|2009-02-05|Toyota Motor Corp|Fuel cell module and fuel cell|
    WO2016097261A1|2014-12-18|2016-06-23|Commissariat A L'energie Atomique Et Aux Energies Alternatives|Elementary module for a reactor performing water electrolysis or h2o/co2 co-electrolysis or an sofc fuel cell and for a catalytic methanation or reforming reactor|
    US20020081471A1|2000-12-22|2002-06-27|Keegan Kevin R.|Fuel cell system incorporating pressure control|
    US6689499B2|2001-09-17|2004-02-10|Siemens Westinghouse Power Corporation|Pressurized solid oxide fuel cell integral air accumular containment|
    FR2957361B1|2010-03-12|2012-04-20|Commissariat Energie Atomique|HIGH TEMPERATURE ELECTROLYSIS WITH ENHANCED OPERATING SAFETY|
    JP6117736B2|2013-06-04|2017-04-19|本田技研工業株式会社|Fuel cell|DE102015215939B4|2015-08-20|2021-02-04|Mtu Friedrichshafen Gmbh|Method for generating a fuel composition and for operating an internal combustion engine|
    DE102017211529A1|2017-07-06|2019-01-10|Mahle International Gmbh|Insert tube for the inlet channel of a plate heat exchanger|
    JP2022516579A|2019-02-18|2022-02-28|フュエルセル エナジー， インコーポレイテッド|Energy storage for combustion turbines using molten carbonate electrolyzer batteries|
    法律状态:
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    2021-09-30| PLFP| Fee payment|Year of fee payment: 6 |
    优先权:
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    US16/335,524| US20190348699A1|2016-09-22|2017-09-15|Methods for co-electrolysis of water and co2or for high-temperature electricity productionoptionally promoting catalytic reactions inside the h2 electrode|
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