WO2016091636A1 - A process for the preparation of ultra-high purity carbon monoxide - Google Patents

A process for the preparation of ultra-high purity carbon monoxide Download PDF

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Publication number
WO2016091636A1
WO2016091636A1 PCT/EP2015/078047 EP2015078047W WO2016091636A1 WO 2016091636 A1 WO2016091636 A1 WO 2016091636A1 EP 2015078047 W EP2015078047 W EP 2015078047W WO 2016091636 A1 WO2016091636 A1 WO 2016091636A1
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Prior art keywords
carbon dioxide
oxygen
stack
solid oxide
catalytic oxidation
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PCT/EP2015/078047
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French (fr)
Inventor
Niklas Bengt Jakobsson
Claus Friis Pedersen
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Haldor Topsøe A/S
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Application filed by Haldor Topsøe A/S filed Critical Haldor Topsøe A/S
Priority to CA2969865A priority Critical patent/CA2969865A1/en
Priority to AU2015359777A priority patent/AU2015359777A1/en
Priority to CN201580066514.XA priority patent/CN107002256A/en
Priority to KR1020177013972A priority patent/KR20170093129A/en
Priority to JP2017527750A priority patent/JP2018505958A/en
Publication of WO2016091636A1 publication Critical patent/WO2016091636A1/en

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    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25BELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B1/00Electrolytic production of inorganic compounds or non-metals
    • C25B1/01Products
    • C25B1/23Carbon monoxide or syngas
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25BELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B1/00Electrolytic production of inorganic compounds or non-metals
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/26Drying gases or vapours
    • B01D53/261Drying gases or vapours by adsorption
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B32/00Carbon; Compounds thereof
    • C01B32/40Carbon monoxide
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25BELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B13/00Diaphragms; Spacing elements
    • C25B13/04Diaphragms; Spacing elements characterised by the material
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25BELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B15/00Operating or servicing cells
    • C25B15/08Supplying or removing reactants or electrolytes; Regeneration of electrolytes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2256/00Main component in the product gas stream after treatment
    • B01D2256/22Carbon dioxide
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/151Reduction of greenhouse gas [GHG] emissions, e.g. CO2

Definitions

  • the present invention relates to a novel process for the preparation of ultra-high purity carbon monoxide (CO) . More specifically, the invention concerns the preparation of a specially treated carbon dioxide (C0 2 ) feed gas for use in a solid oxide electrolysis cell (SOEC) stack to obtain a CO product with ultra-high purity.
  • CO carbon monoxide
  • a solid oxide electrolysis cell is a solid oxide fuel cell (SOFC) run in reverse mode, which uses a solid oxide or ce ⁇ ramic electrolyte to produce e.g. oxygen and hydrogen gas by electrolysis of water. It can also be used to produce CO from carbon dioxide (C0 2 ) , which is led to the fuel side, i.e. the cathode, of the SOEC or SOEC stack with an applied current. As current is applied, the CO 2 is converted to CO, thereby providing an output stream with a high concentration of CO:
  • SOFC solid oxide fuel cell
  • the oxygen side i.e. the anode
  • air, nitrogen or CO 2 is used to flush the oxygen side.
  • the product stream from the SOEC, containing CO mixed with CO 2 is sub ⁇ jected to a separation process such as pressure swing ad ⁇ sorption (PSA) , temperature swing adsorption (TSA) , membrane separation, cryogenic separation or liquid scrubber technology, such as wash with N-methyl-diethanolamine
  • MDEA MDEA to separate CO 2 from the CO product.
  • PSA is espe ⁇ cially suited for the production of high purity CO.
  • Carbon monoxide of high purity is an important raw material for the synthesis of chemicals.
  • Most reactions for the syn ⁇ thesis of chemicals require high temperatures as well as high pressures, and therefore the CO used should have the lowest possible content of carbon dioxide (C0 2 ) which cor ⁇ rodes the reactor by oxidation. Additionally, CO 2 may limit the equilibrium conversion of the reaction in which the produced CO takes part. CO 2 may also inhibit the kinetics of the reaction where CO is used.
  • the purity of the carbon monoxide has to be extremely high. This is for example the case within the semiconductor industry, where the requirements with re- gard to CO gas purity are very strict. In fact, a purity of up to 99.995 % may be required, meaning that maximum con ⁇ centrations of 10 ppm 2 , 15 ppm CO 2 , 6 ppm O 2 , 1 ppm 3 ⁇ 40, 1 ppm 3 ⁇ 4 and 3 ppm CH 4 are allowed. Table 1 below shows the maximum allowable impurity concentrations for CO with puri- ties of 99.95 % and 99.995 %, respectively.
  • US 6,962,629 describes purification of carbon dioxide by catalytic oxi ⁇ dation, where near-critical, critical or supercritical car ⁇ bon dioxide is exposed to at least one catalyst at a tem ⁇ perature controlled to produce carbon dioxide of the de- sired purity, which is less than 10 ppb of non-volatile or ⁇ ganic residues.
  • this US patent does not deal with the removal of volatile impurities, i.e. gases.
  • EP 0 952 111 concerns a system for the removal of traces, i.e. ppm levels, of contaminants in the form of hydrocarbon and sulfur compounds from CO2. This involves the use of a sulfur tolerant catalytic oxidation system which oxidizes the contaminants to carbon dioxide, water and sulfur diox ⁇ ide which are subsequently removed by adsorption and/or ab- sorption techniques. The system is applicable to both car ⁇ bon dioxide production facilities and for on-site CO2 puri ⁇ fication for end-users. In US 6,224,843, a method for the production of pure CO2 from a CO2 off-gas stream from ethylene glycol production is described. This method is also based on catalytic oxida ⁇ tion.
  • WO 2014/154253 discloses a process for producing CO from CO2 in an SOEC stack, where CO2 is led to the fuel side of the stack with an applied current and excess oxygen is transported to the oxygen side of the stack, optionally using air or nitrogen to flush the oxygen side.
  • the product stream from the SOEC, which contains CO mixed with CO2 is subjected to a separation process.
  • the challenge lies in limiting the content of water and hydrogen in the product CO gas. While the CO 2 feed gas can be dried to eliminate water, any traces of hydrocarbons will turn into hydrogen and CO in the SOEC stack as mentioned above, thereby exceeding the allowed maximum of 1 ppm hydrogen in the product CO gas. Furthermore, a methanation activity will also occur in the stack, which may result in the threshold level for methane in the gas being exceeded.
  • the present invention therefore relates to a process for the preparation of carbon monoxide with a purity of at least 99.995 % by electrolysis of pre-treated food grade carbon dioxide, i.e. carbon dioxide with a purity of at least 99.90 %, in a solid oxide electrolysis cell stack, said process comprising the following steps: - mixing food grade carbon dioxide with a minor amount, i.e. 150-250 ppm, of oxygen and heating the mixture,
  • a drying unit more specifically a dryer of mo ⁇ lecular sieve type, placed downstream from the catalytic reactor, the water is removed down to a very low residual water content, leaving a dry CO 2 feed stream with extremely low levels of water and hydrocarbons to be fed to the fuel side of an SOEC based CO plant, optionally together with a purification off-gas recycle (R) .
  • the CO product from the plant has the required purity of 99.995 %.
  • a classical catox catalyst may be used as catalyst for the catalytic oxidation. It consists of Pt and/or Pd on an alumina carrier.
  • the required oxygen for the catalytic oxi ⁇ dation may, as already mentioned, be taken from the oxygen side of the SOEC stack.
  • the water content is preferably removed at the elevated pressure given by the CO2 storage vessel.
  • the surplus of oxygen to be fed to the oxygen side of the SOEC stack should be moderate due to oxidation concerns on the fuel side of the stack.
  • a level of between 150 and 250 ppm in the CO2 feed to the catalytic oxidation is suitable.
  • the CO2 feed stream can be mixed with the PSA recycle stream (CO and CO2 ) , and thus any residual oxy ⁇ gen will be consumed in the SOEC inlet section.
  • the off-gas from the separation process in the plant down- stream of the SOEC stack can be mixed with the CO2 feed up ⁇ stream from the SOEC stack. Thereby, advantages in stack operation may be obtained.
  • the drying of the CO2 feed gas to eliminate water can ad- vantageously be done in a twin vessel dehydrator designed for automatic regeneration (one vessel operating, the other regenerating, each charged with a desiccant) and equipped with built-in heating elements and necessary instruments for the verification of correct regeneration conditions.
  • a typical dehydrator of this kind with a gas flow of 400 kg/h has a total cycle time of 16 hours (8 hours of operation, 7.5 hours of regeneration and 0.5 hours of pressure build ⁇ up and standby) .
  • Each vessel is charged with 100 kg of the preferred desiccant, which has an estimated lifetime of ap- proximately 12000 hours.

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

Abstract

Ultra-high purity (at least 99.995%) carbon monoxide is prepared by electrolysis of pre-treated food grade (at least 99.90%) carbon dioxide in a solid oxide electrolysis cell stack by mixing food grade carbon dioxide with a minor amount (150-250 ppm) of oxygen and heating the mixture, passing the heated mixture through a catalytic oxidation reactor, feeding the hydrocarbon-free effluent from the catalytic oxidation reactor to a drying unit to remove the water to a maximum residual content of 1-3 ppm by volume and feeding the dry, hydrocarbon-free carbon dioxide stream from the drying unit to the fuel side of the solid oxide electrolysis cell stack with an applied current. Excess oxygen is transported to the oxygen side of the stack, and the product stream from the solid oxide electrolysis cell stack is subjected to a separation procedure to remove carbon dioxide from the carbon monoxide product.

Description

Title: A Process for the Preparation of Ultra-High Purity Carbon Monoxide
The present invention relates to a novel process for the preparation of ultra-high purity carbon monoxide (CO) . More specifically, the invention concerns the preparation of a specially treated carbon dioxide (C02) feed gas for use in a solid oxide electrolysis cell (SOEC) stack to obtain a CO product with ultra-high purity.
A solid oxide electrolysis cell is a solid oxide fuel cell (SOFC) run in reverse mode, which uses a solid oxide or ce¬ ramic electrolyte to produce e.g. oxygen and hydrogen gas by electrolysis of water. It can also be used to produce CO from carbon dioxide (C02) , which is led to the fuel side, i.e. the cathode, of the SOEC or SOEC stack with an applied current. As current is applied, the CO2 is converted to CO, thereby providing an output stream with a high concentration of CO:
2 C02 (cathode) -> 2 CO (cathode) + 02 (anode)
Excess oxygen is transported to the oxygen side, i.e. the anode, of the SOEC, and optionally air, nitrogen or CO2 is used to flush the oxygen side. Afterwards the product stream from the SOEC, containing CO mixed with CO2, is sub¬ jected to a separation process such as pressure swing ad¬ sorption (PSA) , temperature swing adsorption (TSA) , membrane separation, cryogenic separation or liquid scrubber technology, such as wash with N-methyl-diethanolamine
(MDEA) to separate CO2 from the CO product. PSA is espe¬ cially suited for the production of high purity CO. Carbon monoxide of high purity is an important raw material for the synthesis of chemicals. Most reactions for the syn¬ thesis of chemicals require high temperatures as well as high pressures, and therefore the CO used should have the lowest possible content of carbon dioxide (C02) which cor¬ rodes the reactor by oxidation. Additionally, CO2 may limit the equilibrium conversion of the reaction in which the produced CO takes part. CO2 may also inhibit the kinetics of the reaction where CO is used.
In some situations, the purity of the carbon monoxide has to be extremely high. This is for example the case within the semiconductor industry, where the requirements with re- gard to CO gas purity are very strict. In fact, a purity of up to 99.995 % may be required, meaning that maximum con¬ centrations of 10 ppm 2, 15 ppm CO2, 6 ppm O2, 1 ppm ¾0, 1 ppm ¾ and 3 ppm CH4 are allowed. Table 1 below shows the maximum allowable impurity concentrations for CO with puri- ties of 99.95 % and 99.995 %, respectively.
Table 1
Maximum allowable impurity concentrations for pure carbon monoxide
CO purity grade, % 99.95 % 99.995 %
oxygen ≤ 100 ppmv ≤ 6 ppmv
nitrogen ≤ 250 ppmv ≤ 10 ppmv
carbon dioxide ≤ 50 ppmv ≤ 15 ppmv
total hydrocarbons ≤ 3 ppmv
methane ≤ 3 ppmv water ≤ 3 ppmv ≤ 1 ppmv
iron pentacarbonyl ≤ 1 ppmv ≤ 0.5 ppmv
hydrogen ≤ 1 ppmv
Obtaining a purity of 99.995 % is not possible without ex¬ traordinary and extensive purification measures for CO pre- pared by a syngas-based synthesis route. Moreover it is al¬ so not possible for CO prepared using a solid oxide elec¬ trolysis cell (SOEC) stack unless extra purification steps are taken. Since CO2 is the starting material for the synthesis of CO in a solid oxide electrolysis cell, it would seem obvious to use very pure CO2 as starting material or to purify CO2 sufficiently to make it suitable for such use. Therefore, in the prior art attempts have been made to find methods to CO2 purification for various purposes. Thus, US 6,962,629 describes purification of carbon dioxide by catalytic oxi¬ dation, where near-critical, critical or supercritical car¬ bon dioxide is exposed to at least one catalyst at a tem¬ perature controlled to produce carbon dioxide of the de- sired purity, which is less than 10 ppb of non-volatile or¬ ganic residues. However, this US patent does not deal with the removal of volatile impurities, i.e. gases.
EP 0 952 111 concerns a system for the removal of traces, i.e. ppm levels, of contaminants in the form of hydrocarbon and sulfur compounds from CO2. This involves the use of a sulfur tolerant catalytic oxidation system which oxidizes the contaminants to carbon dioxide, water and sulfur diox¬ ide which are subsequently removed by adsorption and/or ab- sorption techniques. The system is applicable to both car¬ bon dioxide production facilities and for on-site CO2 puri¬ fication for end-users. In US 6,224,843, a method for the production of pure CO2 from a CO2 off-gas stream from ethylene glycol production is described. This method is also based on catalytic oxida¬ tion. An apparatus for the production of high purity CO, i.e. CO with a purity above 90 %, by electrolysis of CO2 in an SOEC stack is described in WO 2013/131778. It is, however, not rendered probable that said purity above 90 % may extend to 99.995 %.
Finally, WO 2014/154253 discloses a process for producing CO from CO2 in an SOEC stack, where CO2 is led to the fuel side of the stack with an applied current and excess oxygen is transported to the oxygen side of the stack, optionally using air or nitrogen to flush the oxygen side. The product stream from the SOEC, which contains CO mixed with CO2 , is subjected to a separation process.
Even if very pure, i.e. food grade, carbon dioxide (with a purity as specified in Table 2 below) was used as feed for the synthesis of CO in a solid oxide electrolysis cell stack, it would still not be possible to obtain a carbon monoxide end product with a purity of 99.995 % unless extra purification steps would have to be taken, because any traces of different hydrocarbons, which are found even in food grade CO2 , will turn into hydrogen and CO in the SOEC stack, thereby producing more than the requisite maximum of 1 ppm hydrogen.
Table 2
Maximum allowable impurity concentrations for food grade carbon dioxide
Figure imgf000006_0001
To obtain an ultra-high purity carbon monoxide product by SOEC stack electrolysis of CO2 without having to take extra purification steps, the challenge lies in limiting the content of water and hydrogen in the product CO gas. While the CO2 feed gas can be dried to eliminate water, any traces of hydrocarbons will turn into hydrogen and CO in the SOEC stack as mentioned above, thereby exceeding the allowed maximum of 1 ppm hydrogen in the product CO gas. Furthermore, a methanation activity will also occur in the stack, which may result in the threshold level for methane in the gas being exceeded.
It has now turned out that it is possible to use food grade CO2 as feed for an SOEC stack and obtain ultra-high purity CO, if a small amount of pure oxygen is mixed with the feed of food grade CO2 and the resulting mixed stream is led to a catalytic oxidation unit, where the hydrocarbons in the stream are oxidized to CO2 and water. The water is removed in a drying unit downstream from the catalytic oxidation unit, leaving dry, hydrocarbon-free CO2 to be fed to the SOEC stack.
This way it has become possible to use food grade CO2 as feed for an SOEC stack and thereby obtain CO with a purity of 99.995 %.
The present invention therefore relates to a process for the preparation of carbon monoxide with a purity of at least 99.995 % by electrolysis of pre-treated food grade carbon dioxide, i.e. carbon dioxide with a purity of at least 99.90 %, in a solid oxide electrolysis cell stack, said process comprising the following steps: - mixing food grade carbon dioxide with a minor amount, i.e. 150-250 ppm, of oxygen and heating the mixture,
- passing the heated mixture through a catalytic oxidation reactor, wherein the hydrocarbons in the mixture are oxi- dized to carbon dioxide and water,
- feeding the hydrocarbon-free effluent from the catalytic oxidation reactor to a drying unit to remove the water to a maximum residual content of 1-3 ppm by volume and - feeding the dry, hydrocarbon-free carbon dioxide stream from the drying unit to the fuel side of the solid oxide electrolysis cell stack with an applied current, wherein excess oxygen is transported to the oxygen side of the stack, optionally using carbon dioxide, air or nitrogen to flush the oxygen side, and wherein the product stream from the solid oxide electrolysis cell stack is subjected to a separation procedure to remove carbon dioxide from the carbon monoxide product.
The progress of the process according to the invention is illustrated in the appended figure, where food grade CO2 from storage is mixed with a minor amount of pure oxygen, either from a gas bottle (Oxygen 1) or from the oxygen side of the SOEC (Oxygen 2) or both. The mixture is then passed through a catalytic oxidation reactor where the hydrocarbons contained in the CO2 stream are oxidized to CO2 and water. In a drying unit, more specifically a dryer of mo¬ lecular sieve type, placed downstream from the catalytic reactor, the water is removed down to a very low residual water content, leaving a dry CO2 feed stream with extremely low levels of water and hydrocarbons to be fed to the fuel side of an SOEC based CO plant, optionally together with a purification off-gas recycle (R) . The CO product from the plant has the required purity of 99.995 %.
As catalyst for the catalytic oxidation, a classical catox catalyst may be used. It consists of Pt and/or Pd on an alumina carrier. The required oxygen for the catalytic oxi¬ dation may, as already mentioned, be taken from the oxygen side of the SOEC stack. The water content is preferably removed at the elevated pressure given by the CO2 storage vessel. The surplus of oxygen to be fed to the oxygen side of the SOEC stack should be moderate due to oxidation concerns on the fuel side of the stack. A level of between 150 and 250 ppm in the CO2 feed to the catalytic oxidation is suitable. In the SOEC plant the CO2 feed stream can be mixed with the PSA recycle stream (CO and CO2 ) , and thus any residual oxy¬ gen will be consumed in the SOEC inlet section.
The off-gas from the separation process in the plant down- stream of the SOEC stack can be mixed with the CO2 feed up¬ stream from the SOEC stack. Thereby, advantages in stack operation may be obtained.
The drying of the CO2 feed gas to eliminate water can ad- vantageously be done in a twin vessel dehydrator designed for automatic regeneration (one vessel operating, the other regenerating, each charged with a desiccant) and equipped with built-in heating elements and necessary instruments for the verification of correct regeneration conditions. A typical dehydrator of this kind with a gas flow of 400 kg/h has a total cycle time of 16 hours (8 hours of operation, 7.5 hours of regeneration and 0.5 hours of pressure build¬ up and standby) . Each vessel is charged with 100 kg of the preferred desiccant, which has an estimated lifetime of ap- proximately 12000 hours.

Claims

Claims :
1. A process for the preparation of carbon monoxide with a purity of at least 99.995 % by electrolysis of pre- treated food grade carbon dioxide, i.e. carbon dioxide with a purity of at least 99.90 %, in a solid oxide electrolysis cell stack, said process comprising the following steps:
- mixing food grade carbon dioxide with a minor amount, i.e. 150-250 ppm, of oxygen and heating the mixture,
- passing the heated mixture through a catalytic oxidation reactor, wherein the hydrocarbons in the mixture are oxi¬ dized to carbon dioxide and water,
- feeding the hydrocarbon-free effluent from the catalytic oxidation reactor to a drying unit to remove the water to a maximum residual content of 1-3 ppm by volume and - feeding the dry, hydrocarbon-free carbon dioxide stream from the drying unit to the fuel side of the solid oxide electrolysis cell stack with an applied current, wherein excess oxygen is transported to the oxygen side of the stack, optionally using carbon dioxide, air or nitrogen to flush the oxygen side, and wherein the product stream from the solid oxide electrolysis cell stack is subjected to a separation procedure to remove carbon dioxide from the carbon monoxide product.
2. The process according to claim 1, wherein a catalyst consisting of Pt and/or Pd on an alumina carrier is used for the catalytic oxidation.
3. The process according to claim 1, wherein the oxygen required for the catalytic oxidation is taken from the oxy¬ gen side of the SOEC stack.
4. The process according to claim 1, wherein the drying of the carbon dioxide feed gas to eliminate water is done in a twin vessel dehydrator designed for automatic regeneration, where one vessel is operating while the other is re¬ generating, each vessel being charged with a desiccant.
5. The process according to any of the preceding claims, wherein the off-gas from the separation process in the plant downstream of the SOEC stack is mixed with the CO2 feed upstream from the SOEC stack.
PCT/EP2015/078047 2014-12-10 2015-11-30 A process for the preparation of ultra-high purity carbon monoxide WO2016091636A1 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
CA2969865A CA2969865A1 (en) 2014-12-10 2015-11-30 A process for the preparation of ultra-high purity carbon monoxide
AU2015359777A AU2015359777A1 (en) 2014-12-10 2015-11-30 A process for the preparation of ultra-high purity carbon monoxide
CN201580066514.XA CN107002256A (en) 2014-12-10 2015-11-30 A kind of method for the carbon monoxide for preparing ultra-high purity
KR1020177013972A KR20170093129A (en) 2014-12-10 2015-11-30 A process for the preparation of ultra-high purity carbon monoxide
JP2017527750A JP2018505958A (en) 2014-12-10 2015-11-30 Method for producing ultra-high purity carbon monoxide

Applications Claiming Priority (2)

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EP14197083.0A EP3031956B1 (en) 2014-12-10 2014-12-10 A process for the preparation of ultra-high purity carbon monoxide
EP14197083.0 2014-12-10

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JP (1) JP2018505958A (en)
KR (1) KR20170093129A (en)
CN (1) CN107002256A (en)
AU (1) AU2015359777A1 (en)
CA (1) CA2969865A1 (en)
WO (1) WO2016091636A1 (en)

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* Cited by examiner, † Cited by third party
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WO2018228723A1 (en) * 2017-06-16 2018-12-20 Linde Aktiengesellschaft Process and apparatus for manufacturing carbon monoxide
WO2019157507A1 (en) * 2018-02-12 2019-08-15 Lanzatech, Inc. A process for improving carbon conversion efficiency
WO2022136025A1 (en) 2020-12-22 2022-06-30 Topsoe A/S An improved method for operation of a solid oxide electrolysis cell in carbon dioxide electrolysis
EP4123056A1 (en) 2021-07-20 2023-01-25 Topsoe A/S Method for transient operation of a solid oxide electrolysis cell stack
WO2024013029A2 (en) 2022-07-12 2024-01-18 Topsoe A/S Soe plant and process for performing solid oxide electrolysis
US11905173B2 (en) 2018-05-31 2024-02-20 Haldor Topsøe A/S Steam reforming heated by resistance heating

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US20190390901A1 (en) * 2016-12-13 2019-12-26 Linde Aktiengesellschaft Purification process for production of ultra high purity carbon monoxide
JP6162355B1 (en) * 2017-03-22 2017-07-12 東京瓦斯株式会社 Carbon material generation system
WO2018206237A1 (en) * 2017-05-10 2018-11-15 Haldor Topsøe A/S A process for reducing the content of oxygen in metallic copper
CN108439406B (en) * 2018-04-23 2020-03-27 中国科学院上海应用物理研究所 CO recovery and electrolysis2Method and device for preparing CO
BR112021019898A2 (en) * 2019-04-05 2021-12-07 Haldor Topsoe As Ambient air separation and soec front end for ammonia synthesis gas production
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Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0952111A1 (en) 1998-04-24 1999-10-27 Praxair Technology, Inc. CO2 purification system
US6224843B1 (en) 1999-09-13 2001-05-01 Saudi Basic Industries Corporation Carbon dioxide purification in ethylene glycol plants
US6962629B2 (en) 2002-02-19 2005-11-08 Praxair Technology, Inc. Method for moving contaminants from gases
US20070028764A1 (en) * 2005-08-08 2007-02-08 Carsten Wittrup Method for enabling the provision of purified carbon dioxide
US20100284892A1 (en) * 2009-05-06 2010-11-11 American Air Liquide, Inc. Process For The Purification Of A Carbon Dioxide Stream With Heating Value And Use Of This Process In Hydrogen Producing Processes
WO2013131778A2 (en) 2012-03-05 2013-09-12 Haldor Topsøe A/S Apparatus for production of high purity carbon monoxide
WO2014154253A1 (en) 2013-03-26 2014-10-02 Haldor Topsøe A/S A process for producing co from co2 in a solid oxide electrolysis cell

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MY146697A (en) * 2004-07-09 2012-09-14 Acetex Cyprus Ltd Preparation of syngas for acetic acid synthesis by partial oxidation of methanol feedstock
FR2969136A1 (en) * 2010-12-15 2012-06-22 Air Liquide Producing carbon monoxide combined with production of hydrogen from hydrocarbon mixture, by reforming hydrocarbon mixture to obtain synthesis gas, cooling synthesis gas with heat recovery, and extracting carbon dioxide in cooled syngas
KR101477195B1 (en) * 2011-04-22 2014-12-29 부산대학교 산학협력단 Solid oxide fuel cell system equipped with carbon monoxide generator using ultraclean coal or graphite
JP5910539B2 (en) * 2013-02-28 2016-04-27 Jfeスチール株式会社 Method for electrolysis of carbon dioxide gas

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0952111A1 (en) 1998-04-24 1999-10-27 Praxair Technology, Inc. CO2 purification system
US6224843B1 (en) 1999-09-13 2001-05-01 Saudi Basic Industries Corporation Carbon dioxide purification in ethylene glycol plants
US6962629B2 (en) 2002-02-19 2005-11-08 Praxair Technology, Inc. Method for moving contaminants from gases
US20070028764A1 (en) * 2005-08-08 2007-02-08 Carsten Wittrup Method for enabling the provision of purified carbon dioxide
US20100284892A1 (en) * 2009-05-06 2010-11-11 American Air Liquide, Inc. Process For The Purification Of A Carbon Dioxide Stream With Heating Value And Use Of This Process In Hydrogen Producing Processes
WO2013131778A2 (en) 2012-03-05 2013-09-12 Haldor Topsøe A/S Apparatus for production of high purity carbon monoxide
WO2014154253A1 (en) 2013-03-26 2014-10-02 Haldor Topsøe A/S A process for producing co from co2 in a solid oxide electrolysis cell

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2018228723A1 (en) * 2017-06-16 2018-12-20 Linde Aktiengesellschaft Process and apparatus for manufacturing carbon monoxide
WO2019157507A1 (en) * 2018-02-12 2019-08-15 Lanzatech, Inc. A process for improving carbon conversion efficiency
US11359294B2 (en) 2018-02-12 2022-06-14 Lanzatech, Inc. Process for improving carbon conversion efficiency
US11905173B2 (en) 2018-05-31 2024-02-20 Haldor Topsøe A/S Steam reforming heated by resistance heating
WO2022136025A1 (en) 2020-12-22 2022-06-30 Topsoe A/S An improved method for operation of a solid oxide electrolysis cell in carbon dioxide electrolysis
EP4123056A1 (en) 2021-07-20 2023-01-25 Topsoe A/S Method for transient operation of a solid oxide electrolysis cell stack
WO2023001669A1 (en) 2021-07-20 2023-01-26 Topsoe A/S Method for transient operation of a solid oxide electrolysis cell stack
WO2024013029A2 (en) 2022-07-12 2024-01-18 Topsoe A/S Soe plant and process for performing solid oxide electrolysis

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