WO2013131778A2 - Apparatus for production of high purity carbon monoxide - Google Patents

Apparatus for production of high purity carbon monoxide Download PDF

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Publication number
WO2013131778A2
WO2013131778A2 PCT/EP2013/053780 EP2013053780W WO2013131778A2 WO 2013131778 A2 WO2013131778 A2 WO 2013131778A2 EP 2013053780 W EP2013053780 W EP 2013053780W WO 2013131778 A2 WO2013131778 A2 WO 2013131778A2
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WO
WIPO (PCT)
Prior art keywords
solid oxide
oxide electrolysis
stack
gas separation
compartment
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/EP2013/053780
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French (fr)
Other versions
WO2013131778A3 (en
Inventor
Friis Claus PEDERSEN
Bøgild John HANSEN
Thomas Rostrup-Nielsen
Ulrik Jens NIELSEN
Henrik Olsson
Kim Hedegaard Andersen
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Topsoe AS
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Haldor Topsoe AS
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Publication date
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Priority to CN201380013115.8A priority Critical patent/CN104220645B/en
Priority to EA201491624A priority patent/EA201491624A1/en
Priority to JP2014560305A priority patent/JP6192669B2/en
Priority to KR1020147026422A priority patent/KR102080571B1/en
Priority to AU2013229699A priority patent/AU2013229699B2/en
Priority to ES13708114T priority patent/ES2877849T3/en
Priority to EP13708114.7A priority patent/EP2823087B1/en
Priority to US14/382,948 priority patent/US9284651B2/en
Priority to DK13708114.7T priority patent/DK2823087T3/en
Priority to CA2866312A priority patent/CA2866312C/en
Publication of WO2013131778A2 publication Critical patent/WO2013131778A2/en
Publication of WO2013131778A3 publication Critical patent/WO2013131778A3/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B1/00—Electrolytic production of inorganic compounds or non-metals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/10—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction with carbon monoxide
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B1/00—Electrolytic production of inorganic compounds or non-metals
    • C25B1/01—Products
    • C25B1/02—Hydrogen or oxygen
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B1/00—Electrolytic production of inorganic compounds or non-metals
    • C25B1/01—Products
    • C25B1/23—Carbon monoxide or syngas
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B9/00—Cells or assemblies of cells; Constructional parts of cells; Assemblies of constructional parts, e.g. electrode-diaphragm assemblies; Process-related cell features
    • C25B9/05—Pressure cells
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B9/00—Cells or assemblies of cells; Constructional parts of cells; Assemblies of constructional parts, e.g. electrode-diaphragm assemblies; Process-related cell features
    • C25B9/70—Assemblies comprising two or more cells
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/30—Hydrogen technology
    • Y02E60/36—Hydrogen production from non-carbon containing sources, e.g. by water electrolysis

Definitions

  • the present invention concerns an apparatus for production of high purity carbon monoxide, CO, based on electrolysis of carbon dioxide, C02 in combination with a high purity C02 feedstock and gas cleaning operation at temperatures above -100°C.
  • Solid Oxide Electrolysis Cells, SOEC are used for the electrolysing.
  • the proposed invention relates to the production of CO of high purity where the purification relies on simple, low cost purification techniques that do not involve cryogenic tech ⁇ niques .
  • the product gas (CO + H2) is then purified to high purity CO (typically > 99%) in different steps, for instance including a final cryogenic state to separate H2 from the CO and to re ⁇ move possible impurities of N2 and Ar .
  • an object of the present invention to provide an SOEC apparatus and method to produce CO at a lower cost than the presently known techniques. It is a further object of the present invention to provide an SOEC apparatus and method to produce CO at a low cost and at a high purity without the use of cryogenic techniques.
  • the invention relates to a CO production and purification method which is based on C02 electrolysis in combination with simple and in-expensive 'room temperature' gas cleaning and gas separation methods.
  • This invention makes it technically and economically feasible to produce high purity CO in small quantities, for example at the consumption site or at local distribution centres.
  • C02 electrolysis is less known than water electrolysis as fewer techniques are available for C02 electrolysis.
  • One technology which is very efficient for C02 electrolysis is Solid Oxide Electrolysis Cells.
  • the principle of the C02 electrolyser is that C02 (possibly including some CO) is fed to the electrolyser cathode. As current is applied, the C02 is converted to CO to provide an output stream with a high concentration of CO.
  • the output will be con ⁇ verted CO and unconverted C02. If needed, the unconverted C02 can be removed in a C0/C02 separator operating at tempera- tures above -100°C to produce the final high purity CO.
  • an embodiment of this invention includes: ⁇ The use of high purity C02 as feedstock for the electro ⁇ lyser
  • Solvent absorption involves a cyclical process in which C02 or CO is absorbed from a gas stream directed into a liquid, typically water or an amine. Typically, C02 is removed and the processed gas stream is then the final purified CO stream. The absorbent liquid can be processed to remove the C02, which can then be re-used for further electrolysis. The resulting C02-free liquid is used again for absorption and the process continues. This technique is fairly widely used in a range of applications, but it needs a large amount of power to regenerate the solvent. Adsorption is based on a cyclical process in which C02 or CO is adsorbed from a gas stream on to the surface of a solid, typically a mineral zeolite.
  • PSA pressure swing adsorbers
  • Membranes made of polymers or ceramics can be used to effec ⁇ tively sieve out C02 or CO from gas streams.
  • the membrane ma ⁇ terial is specifically designed to preferentially separate the molecules in the mixture.
  • a range of configurations ex- ists either simply as gas separation devices or incorporating liquid absorption stages. This process has not yet been ap ⁇ plied on a large scale and there are challenges related to the composition and temperature of the input gases. Further ⁇ more, the selectivity of the membranes is limited and many recycles will typically be needed to obtain high purity (e.g > 99.5%) gas output.
  • Condensation techniques use low temperatures to cool and con ⁇ dense the C02 from the electrolyser gas streams. Using two coolers where C02 is condensed at one (e.g. at -90°C) and C02 is released from the other (e.g. at -40 C) would allow con- tinuous operation of a condensating C02 removal unit.
  • this invention has a dedicated electro ⁇ lyser design which is used to remove the necessary amount of C02 from the CO + C02 stream.
  • the current which can be applied to all cells in the stack is limited by the flow across the one cell with the minimum flow, such that the maximum current corresponds to a 100% conversion in the cell with minimum flow. If current is applied which would correspond to a conversion rate above 100% for this minimum flow cell, the current would introduce structural changes in the minimum flow cell and the cell would deteriorate quickly together with the stack. Typically this leads to maximum conversion rates of 80% for 70-cell stacks and 90% for 10-cell stacks.
  • the C02 separator can be of any known art as well as a further SOEC as will be disclosed in the following.
  • the separated C02 can be recycled to the input side of the SOEC electrolyser .
  • a scheme which allows SOEC stacks to operate with very high conversion rates to directly produce CO output stream of very high puri- ty (e.g. larger than 90% and e.g. larger than 99%) .
  • This em ⁇ bodiment is based on the individual control of the current across each cell based on monitoring of the voltage across each cell.
  • the voltage across an SOEC cell can be expressed as: where I C eii and R ce ii are the current and resistivity of the relevant cell, respectively.
  • p C o2 Pco and p 0 2 are the partial pressures (in bar) of C02, CO and 02 respectively.
  • an SOEC stack is used for direct production of high purity CO. This is done by monitor ⁇ ing the voltage across each cell and individually adjusting the current across each cell to give a desired cell voltage corresponding to a desired level of C02.
  • This current adjustment scheme can be realised in many ways. This could be by providing a relatively large common current and then removing surplus current with a diode or more flexi ⁇ bly with a transistor and a transistor current controlling circuit. A more energy efficient alternative would be to pro ⁇ vide a relatively low common current and then add additional current (e.g. based on switch mode technology) to obtain the desired cell voltage.
  • additional current e.g. based on switch mode technology
  • the 15% C02 and 85% CO is con- verted to high purity CO e.g. 99.7% CO and 0.3% C02 in a stack where current is controlled individually for the dif ⁇ ferent cells or cell groups.
  • This embodiment is cost effec ⁇ tive as it provides a relative low cost, traditional SOEC stack for the bulk of the C02 conversion and the relative more expensive individual voltage and current control SOEC stack for a small part of the conversion.
  • the main source of such potential impurities is leakages in the SOEC stack. This can be leakages between the cathode and the anode side of the stack and it can be leakages between the stack and the external atmosphere as indicated in fig.5. These types of leakage are often experienced in Solid Oxide stacks. Leakages are caused partly by imperfect sealings be- tween cells and interconnects and partly because small cracks in solid oxide cell electrolytes may easily exist after pro ⁇ duction or may evolve during the system lifetime. If the electrolyser operates with pure oxygen on the anode side, leakages between the anode and the cathode side will not affect the purity of the produced gas (defined as C02 concentration + CO concentration) as oxygen will combust with CO to form C02) .
  • the oxygen side (the an ⁇ ode) is flushed with C02 to reduce the oxygen concentration without reducing the C02 + CO purity of the SOEC output gas- ses even if the SOEC stack is subject to internal leakage.
  • the SOEC stack or stacks are enclosed in a closed compartment which is flushed with C02. This implies that the C02 + CO pu ⁇ rity of the SOEC output gasses are maintained even if the SOEC stack is subject to external leakage.
  • Compartment P0 can further be purged with CO 2 where the purge stream after addition of air is passed through a catalytic oxidation step, see Figure 6.
  • the catalytic oxidation step should comprise a catalyst active in the oxidation reaction between CO and 0 2 .
  • the catalyst could for example be a noble metal catalyst such as Pt and/or Pd optionally combined with V 2 O 5 and WO 3 on an alumina or T1O 2 based carrier.
  • the catalyst should operate above 100 C, preferably between 150 and 250 C to assure elim ⁇ ination of CO emitted to the local environment.
  • the absolute pressure in compartment denoted P0 can be chosen to be set below atmospheric pressure to assure that CO leaking into P0 cannot escape to the surroundings un ⁇ der any circumstances. Improving the purity of the SOEC input gas
  • the polluting gas may affect the operation of or even poison the SOEC or the CO/C02 separation equipment •
  • the polluting gases will in general be separated into the C02 stream. As it is typically advantageous to recycle this stream to the SOEC, the polluting gases may build up in the system
  • Adsorbents or absorbants are used before the SOEC to re- move undesired gas contaminations.
  • sulphur species and solixanes are known to poison Solid Oxide cells. These can be absorbed for example with active carbon or Ni- or Cu-based absorbers.
  • a x purge' can be build into the recycle stream to avoid the accumulation of polluting gases.
  • the recycle stream will typically include CO which in most cases can not be vented safely.
  • One embodiment of this inven ⁇ tion includes a purge outlet of the recycle stream which is combined with oxygen from either air or the oxygen output of the SOEC and where the CO and excess 02 forms
  • CO + CO -> C + C02 Deposition of carbon is thermodynamically advantageous in temperature regions below roughly 700°C and as the CO rich gas cools down carbon may be deposited on for example metal surfaces of pipes or heat exchangers. This may corrode the metal through the mechanism known as metal dusting which eventually may destroy the subjected metal parts.
  • Carbon deposition and metal dusting can be avoided in CO rich environments by using special metals or special coatings of the subjected surfaces.
  • selected metals or coatings are used to avoid carbon formation and metal dusting at the output section of the SOEC electrolyser .
  • This embodiment includes the use of Ni-rich metals such as Inconel or specifically Inconel 693.
  • This embodiment also in ⁇ cludes special coatings of metal surfaces such as surfaces coated with Cu or Sn/Ni coatings for example with 55-65% Sn.
  • a dual tube arrangement In addition to the coatings mentioned, another possibility is to use a dual tube arrangement.
  • a viable option is to insert a copper tube inside a tube with the re ⁇ quired mechanical strength. Copper tubes loose their mechanical strength at elevated temperatures but by applying a cup ⁇ per tube inside a for example a high alloy stainless steel tube and assuring intimate contact between the tube surfaces the mechanical strength of the steel tube can be combined with the resistance towards metal dusting of the copper tube. The protection towards metal dusting is due to that the ma ⁇ jority of the gas is exposed to the Cu surface.
  • a device for production of CO with a purity above 90% when the device is provided with C02 with a purity above 90% said device comprising at least one Solid Oxide Electrolysis Cell with an anode side and a cathode side and said device further comprises an output gas separation unit, wherein the device is operating at temperatures between 0°C - 50°C, pref ⁇ erably at 10°C - 40°, preferably at room temperature.
  • a device comprising a plurality of Solid Oxide Electrolysis Cells arranged in a stack, and wherein said device further comprises means for individual control of the current across selected Solid Oxide Electrolysis Cells.
  • a device wherein said individual control of the current is based on monitoring the voltage across selected Solid Oxide Electrolysis Cells.
  • the output gas separation unit comprises a plurality of cells arranged in a gas separation Solid Oxide Electrolysis Cell stack, and wherein said stack comprises means for individual control of the current across selected cells.
  • the device further comprises means to flush the anode side of the at least one Solid Oxide Electrolysis Cell with C02.
  • the device comprises a compartment enclosing the at least one Solid Oxide Electrolysis Cell, and wherein said compartment comprises means to flush the space enclosed by the compartment .
  • a device wherein the pressure of the cathode side is higher than the pressure of the anode side, the pressure of the anode side is higher than the pres ⁇ sure of the compartment and the pressure of the compartment is below ambient pressure and wherein the compartment is flushed with CO 2 and the CO 2 purge is directed from the com ⁇ partment to a catalytic oxidation reactor utilizing a cata ⁇ lyst comprising a noble metal catalyst such as Pt and or Pd optionally combined with V 2 O 5 and WO 3 on an alumina or T1O 2 based carrier and the catalyst operates above 100°C, prefera ⁇ bly between 150°C and 250°C.
  • a cata ⁇ lyst comprising a noble metal catalyst such as Pt and or Pd optionally combined with V 2 O 5 and WO 3 on an alumina or T1O 2 based carrier and the catalyst operates above 100°C, prefera ⁇ bly between 150°C and 250°C.
  • a device wherein said output gas separation unit is one of, a wa- ter/amine wash, a Pressure Swing Adsorption or selective mem ⁇ branes .
  • said output gas separation unit is one of, a wa- ter/amine wash, a Pressure Swing Adsorption or selective mem ⁇ branes .
  • a device comprising a plurality of stacked Solid Oxide Electrolysis Cells and a plurality of stacks, wherein said stacks are connected in networking connection.
  • a device wherein selected components which are subject to metal dust ⁇ ing are made of Ni-rich metals such as Inconel, preferably Inconel 693, or said components are coated with Cu or Sn/Ni coatings, preferably 55-65% Sn.
  • a device wherein selected components which are subject to metal dust ⁇ ing are made of double tubes; an inner tube which is a copper tube which is placed inside an outer tube with higher mechanical strength than the copper tube, thereby achieving metal dusting protection and simultaneously combining the mechanical strength of the outer tube with the resistance towards metal dusting of the copper tube.
  • a process for production of high purity CO comprising the steps of
  • ⁇ providing said second gas to the output gas separation unit • operating said gas separation unit at temperatures be ⁇ tween 0°C - 50°C, preferably at 10°C - 40°, preferably at room temperature and thereby producing a third output gas comprising CO with a purity above 90%.
  • a process according to claim 13 or 14 further comprising the step of
  • a process according to any of the claims 13-15 further comprising a compartment enclosing the at least one Solid Ox ⁇ ide Electrolysis Cell and further comprising the step of
  • a process according to claim 16 further comprising the step of
  • Fig. 7 shows a schematic diagram of one possible embodiment of the invention.
  • High purity C02 is flushed to both the x fuel' and x oxygen' side of an SOEC stack.
  • the input C02 on the fuel side passes two heat exchangers, while only a single heat exchanger is used on the input side of the x oxygen' side.
  • the reason for this asymmet- ric configuration is that oxygen passes from the fuel to the oxygen side and that the heat capacity therefore is highest on the fuel in and oxygen out streams. This is also reflected in the temperatures and duties of the different heat exchang ⁇ ers as shown in fig. 7.
  • the heat exchanger at the SOEC fuel side is made of either Ni- rich metals such as Inconel, particularly Inconel 693 or coated metal parts e.g. Sn/Ni coated parts.
  • the output temperatures of the heat exchangers closest to the stacks are 675°C and 750°C on the fuel and oxygen side respectively.
  • the SOEC stack is assumed to be operated at the thermo neutral operation point at a temperature of 800 °C. Consequently, the input C02 streams are heated to 800°C in two electrical heaters.
  • a simple variation of this configuration would be to use one electrical heater at the fuel input, heat the stream here to approximately 825°C and let the heat exchanging capacity of the SOEC stack heat up the oxygen side input.
  • the SOEC stack has a capacity to pro ⁇ cute approximately 1.2 Nm3/h CO. This could for example be realised with stacks based on 50 cells with an effective area of 10 x 10 cm. These cells could operate at a current density of the order of 0.75 A/Cm2, a cell voltage of 1.25 V and an effective SOEC conversion efficiency of 3.1 kWh/Nm3.
  • the SOEC cells could be based on a Ni/YSZ support layer, a Ni/YSZ fuel-side electrode a YSZ electrolyte and an LSM elec ⁇ trode on the Oxygen side.
  • the C02 input streams here are chosen to be around 2 Nm3/h at both fuel and oxygen side. This gives a fairly moderate CO concentration of only 63% at the output. This is chosen to allow for a non-uniform flow distribution in the stacks, but much higher output concentrations are possible by using for example individual cell current control.
  • the 2 Nm3/h input flow to the Oxygen side is chosen to assure an 02 concentration well below 50% at the output. This reduc ⁇ es the speed of corrosion on the oxygen side output and sim ⁇ plifies the choice of materials for heat exchangers and pip- ing .
  • the gas stream is cooled and the ma ⁇ jority of the CO is being removed in a separator, which for example could be based on membranes.
  • the remaining C02 is in this example just send into the air but could also be recy ⁇ cled (including some possible fraction of CO) into the fuel side input.
  • a fraction of the SOEC out ⁇ put is recycled to the input, where the residual CO may also help to avoid oxidation at the input of the fuel side of the SOEC stack.
  • Fig. 8 shows an example of stack networking.
  • the lower stack is made up by 20 cells, the upper one by 10 cells.
  • the bottom of both stacks is in this case facing the internal manifold plate .
  • Fig. 9 shows the importance of actively handling the possible impurities introduced in the output stream of an SOEC system by stack leakages.
  • Test 1 shows the impurities (N2 and 02) of a stack operating with uniform pressure and with air used for flushing the oxygen side.
  • C02 was used instead of air to flush the oxygen side and in this case the impurity level have been reduced from roughly 1.5 mole% to less than 0.75 mole%.
  • the pressure of the fuel side (the cathode) has been increased to be roughly 100 mbar higher than on the oxygen side and in the external stack compartment.
  • C02 was used for flushing the oxygen side.
  • the impurity level was below 0.3 mole% which is sufficient for meeting for exam- pie the standard industrial grade for bottled CO.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Inorganic Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
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Abstract

A device and a process for producing high purity CO by electrolysis of C02 in a Solid Oxide Electrolysis Cell stack and a gas separation unit, also the gas separation unit may be a Solid Oxide Electrolysis Cell stack.

Description

Title: Apparatus for production of high purity Carbon Monoxide
The present invention concerns an apparatus for production of high purity carbon monoxide, CO, based on electrolysis of carbon dioxide, C02 in combination with a high purity C02 feedstock and gas cleaning operation at temperatures above -100°C. In particular, Solid Oxide Electrolysis Cells, SOEC, are used for the electrolysing.
The proposed invention relates to the production of CO of high purity where the purification relies on simple, low cost purification techniques that do not involve cryogenic tech¬ niques .
Traditionally CO is produced on commercial scale by reforming hydro-carbons, e.g.:
CH4 + H20 -> CO + 4H2
or
4CH4 + 02 + 2H20 → 10H2 + 4CO
The product gas (CO + H2) is then purified to high purity CO (typically > 99%) in different steps, for instance including a final cryogenic state to separate H2 from the CO and to re¬ move possible impurities of N2 and Ar .
CO boils at -205°C, H2 at -252.87°C and this cryogenic pro¬ cess is therefore very expensive and has to be carried out at large central facilities. This leads to long distribution paths between the CO production site and the end user and with CO being a poisonous gas, subject to strict safety re- quirements during handling, transportation and storage, this add significantly to the cost. Consequently, the price for smaller quantities (e.g. < 100 Nm3/h) of high purity CO is 5- 10 times higher than the price of the H2 produced in the same reforming process.
It is an object of the present invention to provide an appa¬ ratus and a method for the production of CO which solves the above mentioned problems.
More specifically it is an object of the present invention to provide an SOEC apparatus and method to produce CO at a lower cost than the presently known techniques. It is a further object of the present invention to provide an SOEC apparatus and method to produce CO at a low cost and at a high purity without the use of cryogenic techniques.
The invention relates to a CO production and purification method which is based on C02 electrolysis in combination with simple and in-expensive 'room temperature' gas cleaning and gas separation methods. This invention makes it technically and economically feasible to produce high purity CO in small quantities, for example at the consumption site or at local distribution centres.
C02 electrolysis is less known than water electrolysis as fewer techniques are available for C02 electrolysis. One technology which is very efficient for C02 electrolysis is Solid Oxide Electrolysis Cells. The principle of the C02 electrolyser is that C02 (possibly including some CO) is fed to the electrolyser cathode. As current is applied, the C02 is converted to CO to provide an output stream with a high concentration of CO.
2C02 (cathode) -> 2CO (cathode) + 02 (anode)
If pure C02 is inserted into the SOEC the output will be con¬ verted CO and unconverted C02. If needed, the unconverted C02 can be removed in a C0/C02 separator operating at tempera- tures above -100°C to produce the final high purity CO.
One particular issue with the known gas separator techniques operating at temperatures above -100 C is that they in gen¬ eral are only selective to one or a few molecules and hence have difficulties in removing for example Ar or N2 from the CO + C02 electrolyser output stream.
Consequently an embodiment of this invention includes: · The use of high purity C02 as feedstock for the electro¬ lyser
• Operating the SOEC electrolyser in schemes where impurities are not added to the product stream even if leak¬ ages are present in the electrolyser stack.
Here purity is defined as: Concentration (C02) + Concentra¬ tion (CO) .
Gas Separation
Four commonly known technologies exist for separating C02 or CO from a gas stream. These can be characterised as absorp- tion, adsorption, membrane filtering and condensation methods and can all be used for the present invention.
Solvent absorption involves a cyclical process in which C02 or CO is absorbed from a gas stream directed into a liquid, typically water or an amine. Typically, C02 is removed and the processed gas stream is then the final purified CO stream. The absorbent liquid can be processed to remove the C02, which can then be re-used for further electrolysis. The resulting C02-free liquid is used again for absorption and the process continues. This technique is fairly widely used in a range of applications, but it needs a large amount of power to regenerate the solvent. Adsorption is based on a cyclical process in which C02 or CO is adsorbed from a gas stream on to the surface of a solid, typically a mineral zeolite. Typically, C02 is removed and the processed gas stream is then the final purified CO stream. The solid is then purified in stages using differ- ences in either pressure or temperature to remove the C02. Common adsorbing technologies are the so-called pressure swing adsorbers (PSA) , which are widely used in industry, but may be quite expensive for small scale (< 2000 Nm3/h) opera¬ tion.
Membranes made of polymers or ceramics, can be used to effec¬ tively sieve out C02 or CO from gas streams. The membrane ma¬ terial is specifically designed to preferentially separate the molecules in the mixture. A range of configurations ex- ists either simply as gas separation devices or incorporating liquid absorption stages. This process has not yet been ap¬ plied on a large scale and there are challenges related to the composition and temperature of the input gases. Further¬ more, the selectivity of the membranes is limited and many recycles will typically be needed to obtain high purity (e.g > 99.5%) gas output.
Condensation techniques use low temperatures to cool and con¬ dense the C02 from the electrolyser gas streams. Using two coolers where C02 is condensed at one (e.g. at -90°C) and C02 is released from the other (e.g. at -40 C) would allow con- tinuous operation of a condensating C02 removal unit.
SOEC based gas cleaning.
As an alternative to the above mentioned traditional gas- cleaning techniques, this invention has a dedicated electro¬ lyser design which is used to remove the necessary amount of C02 from the CO + C02 stream.
In the following a range of embodiments according to the in- vention will be described and their advantages will be ex¬ plained .
In principle, all C02 fed to an electrolyser can be converted to CO by applying the correct current and voltage to the cells. Typically, the practical limitation to high conversion ratio is that a stack operates with a single current going through the stack and with slightly non-uniform gas flows between the different cells in the stack. Fig. 2 shows schemat¬ ically the gas and current flows of a stack. The gas is fed at the bottom and then propagates upwards in the stack to cross the cells. Due to pressure loss in the upward flow channels and inevitable differences in the pressure loss across different cells there will always be some variations in the flows across the different cells.
The current which can be applied to all cells in the stack is limited by the flow across the one cell with the minimum flow, such that the maximum current corresponds to a 100% conversion in the cell with minimum flow. If current is applied which would correspond to a conversion rate above 100% for this minimum flow cell, the current would introduce structural changes in the minimum flow cell and the cell would deteriorate quickly together with the stack. Typically this leads to maximum conversion rates of 80% for 70-cell stacks and 90% for 10-cell stacks. In one embodiment of the present invention as shown in fig. 1 it is necessary to separate the CO from the C02 after the SOEC electrolysis of the input gas of high purity C02. The C02 separator can be of any known art as well as a further SOEC as will be disclosed in the following. The separated C02 can be recycled to the input side of the SOEC electrolyser .
In a further embodiment of the invention a scheme is proposed which allows SOEC stacks to operate with very high conversion rates to directly produce CO output stream of very high puri- ty (e.g. larger than 90% and e.g. larger than 99%) . This em¬ bodiment is based on the individual control of the current across each cell based on monitoring of the voltage across each cell. The voltage across an SOEC cell can be expressed as:
Figure imgf000008_0001
where ICeii and Rceii are the current and resistivity of the relevant cell, respectively. pCo2, Pco and p02 are the partial pressures (in bar) of C02, CO and 02 respectively.
This implies that as the fraction of C02 in the gas decreas¬ es, the voltage across each cell increases quite significant- ly.
In an embodiment of this invention an SOEC stack is used for direct production of high purity CO. This is done by monitor¬ ing the voltage across each cell and individually adjusting the current across each cell to give a desired cell voltage corresponding to a desired level of C02.
This is shown in fig. 3, where a stack is fed with a nonuniform flow of C02 and one common current Icommon- The current through each cell (e.g. cell xi')is then adjusted (with the current Δΐι) to provide a cell specific current (e.g. Ii = Icommon + Δΐι) which results in the desired voltage (e.g. Vref) and hence CO concentration across the individual cells.
This current adjustment scheme can be realised in many ways. This could be by providing a relatively large common current and then removing surplus current with a diode or more flexi¬ bly with a transistor and a transistor current controlling circuit. A more energy efficient alternative would be to pro¬ vide a relatively low common current and then add additional current (e.g. based on switch mode technology) to obtain the desired cell voltage. In a further embodiment of this invention as shown in fig. 4, the individual voltage and current control is only applied to the last stage of the C02 to CO conversion. The bulk of the C02 conversion is then performed in traditional stacks where all cells are operating at the same current. This could for example be the conversion of a 100% C02 stream to 15% C02 and 85% CO in traditional stack operating solely with common currents for all cells. In a second stage (typically involving fewer cells and higher flows) the 15% C02 and 85% CO is con- verted to high purity CO e.g. 99.7% CO and 0.3% C02 in a stack where current is controlled individually for the dif¬ ferent cells or cell groups. This embodiment is cost effec¬ tive as it provides a relative low cost, traditional SOEC stack for the bulk of the C02 conversion and the relative more expensive individual voltage and current control SOEC stack for a small part of the conversion.
Avoiding SOEC stack related impurities To avoid expensive C02 separation at the output stage of this invention, it is critical that the SOEC electrolyser does not add impurities to the gas stream.
The main source of such potential impurities is leakages in the SOEC stack. This can be leakages between the cathode and the anode side of the stack and it can be leakages between the stack and the external atmosphere as indicated in fig.5. These types of leakage are often experienced in Solid Oxide stacks. Leakages are caused partly by imperfect sealings be- tween cells and interconnects and partly because small cracks in solid oxide cell electrolytes may easily exist after pro¬ duction or may evolve during the system lifetime. If the electrolyser operates with pure oxygen on the anode side, leakages between the anode and the cathode side will not affect the purity of the produced gas (defined as C02 concentration + CO concentration) as oxygen will combust with CO to form C02) . However, high purity oxygen is very difficult to handle at the high temperatures around 800 °C where it is generated in an SOEC electrolysor . These issues are relat¬ ed to corrosion and possibly even to combustion of the high temperature metal parts. It can therefore be attractive to flush the oxygen side of the electrolysor to reduce the oxy¬ gen concentration.
In an embodiment of this invention the oxygen side (the an¬ ode) is flushed with C02 to reduce the oxygen concentration without reducing the C02 + CO purity of the SOEC output gas- ses even if the SOEC stack is subject to internal leakage.
In a further embodiment of this invention as shown in fig. 6, the SOEC stack or stacks are enclosed in a closed compartment which is flushed with C02. This implies that the C02 + CO pu¬ rity of the SOEC output gasses are maintained even if the SOEC stack is subject to external leakage.
In a further embodiment of this invention, different compart- ments of SOEC stacks are operated at different pressures. If the pressure on the anode (02) side is PI, the pressure on the cathode (C02) side is P2 and the pressure outside the stack is P0, then the stack could for example be operated at conditions where:
P0 < PI < P2 This will assure that very few impurities penetrates from the external side into the stack and that very few impurities diffuses from the anode side into cathode side, where the CO is produced.
Compartment P0 can further be purged with CO2 where the purge stream after addition of air is passed through a catalytic oxidation step, see Figure 6. The catalytic oxidation step should comprise a catalyst active in the oxidation reaction between CO and 02.
2CO + 02 -> 2C02
The catalyst could for example be a noble metal catalyst such as Pt and/or Pd optionally combined with V2O5 and WO3 on an alumina or T1O2 based carrier. The catalyst should operate above 100 C, preferably between 150 and 250 C to assure elim¬ ination of CO emitted to the local environment. In addition, the absolute pressure in compartment denoted P0 can be chosen to be set below atmospheric pressure to assure that CO leaking into P0 cannot escape to the surroundings un¬ der any circumstances. Improving the purity of the SOEC input gas
To avoid the use of a very expensive C02 feedstock, this in¬ vention has to take into account that the C02 feedgas have some contents of undesired "polluting" gasses. This can have two undesirable effects on the system:
• The polluting gas may affect the operation of or even poison the SOEC or the CO/C02 separation equipment • For a well designed CO/C02 separation equipment the polluting gases will in general be separated into the C02 stream. As it is typically advantageous to recycle this stream to the SOEC, the polluting gases may build up in the system
To address these potential issues the present inventions in¬ cludes embodiments as seen on Fig. 10 where:
• Adsorbents or absorbants are used before the SOEC to re- move undesired gas contaminations. In particular sulphur species and solixanes are known to poison Solid Oxide cells. These can be absorbed for example with active carbon or Ni- or Cu-based absorbers.
• A xpurge' can be build into the recycle stream to avoid the accumulation of polluting gases. However, the recycle stream will typically include CO which in most cases can not be vented safely. One embodiment of this inven¬ tion includes a purge outlet of the recycle stream which is combined with oxygen from either air or the oxygen output of the SOEC and where the CO and excess 02 forms
C02 on an oxidizing catalyst (CatOx) .
Avoiding carbon formation and metal dusting
One practical issue in relation to high purity CO producing devices operating at elevated temperatures is that carbon may be formed from carbon monoxide through the so-called Bou- douard reaction:
CO + CO -> C + C02 Deposition of carbon is thermodynamically advantageous in temperature regions below roughly 700°C and as the CO rich gas cools down carbon may be deposited on for example metal surfaces of pipes or heat exchangers. This may corrode the metal through the mechanism known as metal dusting which eventually may destroy the subjected metal parts.
Carbon deposition and metal dusting can be avoided in CO rich environments by using special metals or special coatings of the subjected surfaces. In a special embodiment of this in- vention, selected metals or coatings are used to avoid carbon formation and metal dusting at the output section of the SOEC electrolyser .
This embodiment includes the use of Ni-rich metals such as Inconel or specifically Inconel 693. This embodiment also in¬ cludes special coatings of metal surfaces such as surfaces coated with Cu or Sn/Ni coatings for example with 55-65% Sn.
In addition to the coatings mentioned, another possibility is to use a dual tube arrangement. In the case of Cu a viable option is to insert a copper tube inside a tube with the re¬ quired mechanical strength. Copper tubes loose their mechanical strength at elevated temperatures but by applying a cup¬ per tube inside a for example a high alloy stainless steel tube and assuring intimate contact between the tube surfaces the mechanical strength of the steel tube can be combined with the resistance towards metal dusting of the copper tube. The protection towards metal dusting is due to that the ma¬ jority of the gas is exposed to the Cu surface. Small por- tions of gas may find its way to compartments caused by im¬ perfections in the lining but the metal dusting potent gas in these compartments is stagnant and can thus only have an in- significant effect on the metal surface. This is especially advantageous in applications operating close to atmospheric pressures as the forces separating the tubes at a system pressure reduction are directly dependant on the pressure level in the system.
Features of the invention 1. A device for production of CO with a purity above 90% when the device is provided with C02 with a purity above 90%, said device comprising at least one Solid Oxide Electrolysis Cell with an anode side and a cathode side and said device further comprises an output gas separation unit, wherein the device is operating at temperatures between 0°C - 50°C, pref¬ erably at 10°C - 40°, preferably at room temperature.
2. A device according to claim 1, wherein said device comprises a plurality of Solid Oxide Electrolysis Cells arranged in a stack, and wherein said device further comprises means for individual control of the current across selected Solid Oxide Electrolysis Cells.
3. A device according to claim 2, wherein said individual control of the current is based on monitoring the voltage across selected Solid Oxide Electrolysis Cells.
4. A device according to claim 2 or 3, wherein the output gas separation unit is integrated in said stack.
5. A device according to any of the claims 1 to 3, wherein the output gas separation unit comprises a plurality of cells arranged in a gas separation Solid Oxide Electrolysis Cell stack, and wherein said stack comprises means for individual control of the current across selected cells. 6. A device according to any of the preceding claims, wherein the device further comprises means to flush the anode side of the at least one Solid Oxide Electrolysis Cell with C02. 7. A device according to any of the preceding claims, wherein the device comprises a compartment enclosing the at least one Solid Oxide Electrolysis Cell, and wherein said compartment comprises means to flush the space enclosed by the compartment .
8. A device according to claim 7, wherein the pressure of the cathode side is higher than the pressure of the anode side, the pressure of the anode side is higher than the pres¬ sure of the compartment and the pressure of the compartment is below ambient pressure and wherein the compartment is flushed with CO2 and the CO2 purge is directed from the com¬ partment to a catalytic oxidation reactor utilizing a cata¬ lyst comprising a noble metal catalyst such as Pt and or Pd optionally combined with V2O5 and WO3 on an alumina or T1O2 based carrier and the catalyst operates above 100°C, prefera¬ bly between 150°C and 250°C.
9. A device according to any of the preceding claims, wherein said output gas separation unit is one of, a wa- ter/amine wash, a Pressure Swing Adsorption or selective mem¬ branes . 10. A device according to any of the preceding claims comprising a plurality of stacked Solid Oxide Electrolysis Cells and a plurality of stacks, wherein said stacks are connected in networking connection.
11. A device according to any of the preceding claims, wherein selected components which are subject to metal dust¬ ing are made of Ni-rich metals such as Inconel, preferably Inconel 693, or said components are coated with Cu or Sn/Ni coatings, preferably 55-65% Sn.
12. A device according to any of the preceding claims, wherein selected components which are subject to metal dust¬ ing are made of double tubes; an inner tube which is a copper tube which is placed inside an outer tube with higher mechanical strength than the copper tube, thereby achieving metal dusting protection and simultaneously combining the mechanical strength of the outer tube with the resistance towards metal dusting of the copper tube.
13. A process for production of high purity CO comprising the steps of
• providing a first C02 gas with a purity above 90% to a device comprising at least one Solid Oxide Electrolysis Cell and comprising a gas separation unit
• providing a current to at least one Solid Oxide Elec¬ trolysis Cell and producing a second gas comprising CO in said Solid Oxide Electrolysis cell by means of C02 electrolysis
· providing said second gas to the output gas separation unit • operating said gas separation unit at temperatures be¬ tween 0°C - 50°C, preferably at 10°C - 40°, preferably at room temperature and thereby producing a third output gas comprising CO with a purity above 90%.
14. A process according to claim 13, wherein said device comprises a plurality of Solid Oxide Electrolysis Cells ar¬ ranged in a stack, and which process further comprises the step of
• individually controlling the current across selected
Solid Oxide Electrolysis Cells
15. A process according to claim 13 or 14 further comprising the step of
• flushing the anode side of the at least one Solid Oxide Electrolysis Cell with C02.
16. A process according to any of the claims 13-15 further comprising a compartment enclosing the at least one Solid Ox¬ ide Electrolysis Cell and further comprising the step of
• flushing the space enclosed by said compartment.
17. A process according to claim 16 further comprising the step of
• controlling the pressure in the compartment, the anode chambers of the Solid Oxide Electrolysis Cells and the cathode chambers of the Solid Oxide Electrolysis Cells to different levels to reduce diffusion into the cathode chambers .
18. A process according to any of the claims 13-16 wherein the said gas separation comprises the steps • providing said second gas to a gas separation Solid Ox¬ ide Electrolysis Cell stack
• controlling the current across each individual cell in said gas separation Solid Oxide Electrolysis Cell stack.
19. Process according to any of the claims 13-18 for the production of CO with a purity above 95%, preferably above 99%, preferably above 99.5%. 20. Use of CO as prepared by a device according to any of the claims 1-12 for the production of CH3COOH.
Examples Complete system
Fig. 7 shows a schematic diagram of one possible embodiment of the invention. High purity C02 is flushed to both the xfuel' and xoxygen' side of an SOEC stack. To recuperate most of the heat from the system, the input C02 on the fuel side passes two heat exchangers, while only a single heat exchanger is used on the input side of the xoxygen' side. The reason for this asymmet- ric configuration is that oxygen passes from the fuel to the oxygen side and that the heat capacity therefore is highest on the fuel in and oxygen out streams. This is also reflected in the temperatures and duties of the different heat exchang¬ ers as shown in fig. 7.
To avoid metal dusting and carbon formation the heat exchanger at the SOEC fuel side (cathode side) is made of either Ni- rich metals such as Inconel, particularly Inconel 693 or coated metal parts e.g. Sn/Ni coated parts.
With this configuration the output temperatures of the heat exchangers closest to the stacks are 675°C and 750°C on the fuel and oxygen side respectively. The SOEC stack is assumed to be operated at the thermo neutral operation point at a temperature of 800 °C. Consequently, the input C02 streams are heated to 800°C in two electrical heaters. A simple variation of this configuration would be to use one electrical heater at the fuel input, heat the stream here to approximately 825°C and let the heat exchanging capacity of the SOEC stack heat up the oxygen side input. In this configuration, the SOEC stack has a capacity to pro¬ duce approximately 1.2 Nm3/h CO. This could for example be realised with stacks based on 50 cells with an effective area of 10 x 10 cm. These cells could operate at a current density of the order of 0.75 A/Cm2, a cell voltage of 1.25 V and an effective SOEC conversion efficiency of 3.1 kWh/Nm3.
The SOEC cells could be based on a Ni/YSZ support layer, a Ni/YSZ fuel-side electrode a YSZ electrolyte and an LSM elec¬ trode on the Oxygen side. The C02 input streams here are chosen to be around 2 Nm3/h at both fuel and oxygen side. This gives a fairly moderate CO concentration of only 63% at the output. This is chosen to allow for a non-uniform flow distribution in the stacks, but much higher output concentrations are possible by using for example individual cell current control. The 2 Nm3/h input flow to the Oxygen side is chosen to assure an 02 concentration well below 50% at the output. This reduc¬ es the speed of corrosion on the oxygen side output and sim¬ plifies the choice of materials for heat exchangers and pip- ing .
At the fuel side output, the gas stream is cooled and the ma¬ jority of the CO is being removed in a separator, which for example could be based on membranes. The remaining C02 is in this example just send into the air but could also be recy¬ cled (including some possible fraction of CO) into the fuel side input. In this configuration a fraction of the SOEC out¬ put is recycled to the input, where the residual CO may also help to avoid oxidation at the input of the fuel side of the SOEC stack.
Stack networking example
Fig. 8 shows an example of stack networking. The lower stack is made up by 20 cells, the upper one by 10 cells. The bottom of both stacks is in this case facing the internal manifold plate .
Avoiding contaminations from SOEC stack leakages
Fig. 9 shows the importance of actively handling the possible impurities introduced in the output stream of an SOEC system by stack leakages.
Test 1 shows the impurities (N2 and 02) of a stack operating with uniform pressure and with air used for flushing the oxygen side. In test 2 C02 was used instead of air to flush the oxygen side and in this case the impurity level have been reduced from roughly 1.5 mole% to less than 0.75 mole%. In test 3, the pressure of the fuel side (the cathode) has been increased to be roughly 100 mbar higher than on the oxygen side and in the external stack compartment. C02 was used for flushing the oxygen side. In this test the impurity level was below 0.3 mole% which is sufficient for meeting for exam- pie the standard industrial grade for bottled CO.

Claims

1. A device for production of CO with a purity above 90% when the device is provided with C02 with a purity above 90%, said device comprising at least one Solid Oxide Electrolysis Cell with an anode side and a cathode side and said device further comprises an output gas separation unit, wherein the device is operating at temperatures between 0°C - 50°C, pref¬ erably at 10°C - 40° .
2. A device according to claim 1, wherein said device comprises a plurality of Solid Oxide Electrolysis Cells arranged in a stack, and wherein said device further comprises means for individual control of the current across selected Solid Oxide Electrolysis Cells.
3. A device according to claim 2, wherein said individual control of the current is based on monitoring the voltage across selected Solid Oxide Electrolysis Cells.
4. A device according to claim 2 or 3, wherein the output gas separation unit is integrated in said stack.
5. A device according to any of the claims 1 to 3, wherein the output gas separation unit comprises a plurality of cells arranged in a gas separation Solid Oxide Electrolysis Cell stack, and wherein said stack comprises means for individual control of the current across selected cells.
6. A device according to any of the preceding claims, wherein the device further comprises means to flush the anode side of the at least one Solid Oxide Electrolysis Cell with C02.
7. A device according to any of the preceding claims, wherein the device comprises a compartment enclosing the at least one Solid Oxide Electrolysis Cell, and wherein said compartment comprises means to flush the space enclosed by the compartment .
8. A device according to claim 7, wherein the pressure of the cathode side is higher than the pressure of the anode side, the pressure of the anode side is higher than the pres¬ sure of the compartment and the pressure of the compartment is below ambient pressure and wherein the compartment is flushed with CO2 and the CO2 purge is directed from the com¬ partment to a catalytic oxidation reactor utilizing a cata¬ lyst comprising a noble metal catalyst such as Pt and or Pd optionally combined with V2O5 and WO3 on an alumina or T1O2 based carrier and the catalyst operates above 100°C, prefera- bly between 150°C and 250°C.
9. A device according to any of the preceding claims, wherein said output gas separation unit is one of, a wa- ter/amine wash, a Pressure Swing Adsorption or selective mem- branes.
10. A device according to any of the preceding claims comprising a plurality of stacked Solid Oxide Electrolysis Cells and a plurality of stacks, wherein said stacks are connected in networking connection.
11. A device according to any of the preceding claims, wherein selected components which are subject to metal dust¬ ing are made of Ni-rich metals such as Inconel, preferably Inconel 693, or said components are coated with Cu or Sn/Ni coatings, preferably 55-65% Sn.
12. A device according to any of the preceding claims, wherein selected components which are subject to metal dust¬ ing are made of double tubes; an inner tube which is a copper tube which is placed inside an outer tube with higher mechanical strength than the copper tube, thereby achieving metal dusting protection and simultaneously combining the mechanical strength of the outer tube with the resistance towards metal dusting of the copper tube.
13. A process for production of high purity CO comprising the steps of
• providing a first C02 gas with a purity above 90% to a device comprising at least one Solid Oxide Electrolysis Cell and comprising a gas separation unit
• providing a current to at least one Solid Oxide Elec¬ trolysis Cell and producing a second gas comprising CO in said Solid Oxide Electrolysis cell by means of C02 electrolysis
· providing said second gas to the output gas separation unit
• operating said gas separation unit at temperatures be¬ tween 0°C - 50°C, preferably at 10°C - 40° and thereby producing a third output gas comprising CO with a purity above 90%.
14. A process according to claim 13, wherein said device comprises a plurality of Solid Oxide Electrolysis Cells ar¬ ranged in a stack, and which process further comprises the step of
• individually controlling the current across selected
Solid Oxide Electrolysis Cells
15. A process according to claim 13 or 14 further comprising the step of
• flushing the anode side of the at least one Solid Oxide Electrolysis Cell with C02.
16. A process according to any of the claims 13-15 further comprising a compartment enclosing the at least one Solid Ox¬ ide Electrolysis Cell and further comprising the step of
• flushing the space enclosed by said compartment.
17. A process according to claim 16 further comprising the step of
• controlling the pressure in the compartment, the anode chambers of the Solid Oxide Electrolysis Cells and the cathode chambers of the Solid Oxide Electrolysis Cells to different levels to reduce diffusion into the cathode chambers .
18. A process according to any of the claims 13-16 wherein the said gas separation comprises the steps
• providing said second gas to a gas separation Solid Ox¬ ide Electrolysis Cell stack
• controlling the current across each individual cell in said gas separation Solid Oxide Electrolysis Cell stack.
19. Process according to any of the claims 13-18 for the production of CO with a purity above 95%, preferably above 99%, preferably above 99.5%.
20. Use of CO as prepared by a device according to any of the claims 1-12 for the production of CH3COOH.
PCT/EP2013/053780 2012-03-05 2013-02-26 Apparatus for production of high purity carbon monoxide Ceased WO2013131778A2 (en)

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