Membrane reactor
US-9217202-B2 · Dec 22, 2015 · US
US2018195184A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2018195184-A1 |
| Application number | US-201615739736-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jul 30, 2016 |
| Priority date | Jul 3, 2015 |
| Publication date | Jul 12, 2018 |
| Grant date | — |
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The present disclosure relates to electrolysis. The teachings thereof may be embodied in a reduction process and/or an electrolysis system for electrochemical carbon dioxide utilization wherein carbon dioxide is introduced into an electrolysis cell and reduced at a cathode. For example, an electrolysis system for carbon dioxide utilization may comprise: an electrolyzer including an anode in an anode space and a cathode in a cathode space. The cathode space has an entrance for carbon dioxide. The cathode space comprises a catholyte including alkali metal cations. The anode space has an entrance for an anolyte. The anode space comprises an anolyte comprising chlorine anions.
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What is claimed is: 1 . An electrolysis system for carbon dioxide utilization, the system comprising: an electrolyzer including an anode in an anode space and a cathode in a cathode space; the cathode space has an entrance for carbon dioxide; the cathode space comprises a catholyte including alkali metal cations; the anode space has an entrance for an anolyte; the anode space comprises an anolyte comprising chlorine anions. 2 . The electrolysis system as claimed in claim 1 , further comprising a deposition tank configured for crystallization of an alkali metal hydrogencarbonate and/or alkali metal carbonate out of the catholyte; wherein the deposition tank includes a product outlet. 3 . The electrolysis system as claimed in claim 2 , further comprising a cooling apparatus for the deposition tank. 4 . The electrolysis system as claimed in claim 2 , further comprising a reservoir connected to the cathode space or the deposition tank to buffer the catholyte. 5 . The electrolysis system as claimed in claim 1 , wherein the catholyte comprises a solvent. 6 . The electrolysis system as claimed in claim 1 , wherein the anolyte includes at least one water-soluble alkali metal salt. 7 . The electrolysis system as claimed in claim 1 , further comprising the anode space connected to a gas separation unit for separation of chlorine gas from the anolyte. 8 . The electrolysis system as claimed in claim 1 , further comprising a cation-conducting membrane separating the anode space and cathode space from one another. 9 . A reduction process for carbon dioxide utilization, the process comprising: introducing a catholyte and carbon dioxide into a cathode space with a cathode; reducing carbon dioxide at the cathode; introducing an anolyte including chloride anions into an anode space and brought into contact with an anode; wherein the anolyte includes alkali metal cations that migrate into the catholyte; oxidizing chloride anions at the anode to chlorine; separating chlorine from the anolyte as chlorine gas using a gas separation unit; and introducing at least a portion of the catholyte volume into a deposition tank, where an alkali metal hydrogencarbonate and/or alkali metal carbonate crystallizes out. 10 . The reduction process as claimed in claim 9 , further including reducing, at the cathode, carbon dioxide (CO 2 ) to carbon monoxide (CO), ethylene (C 2 H 4 ), methane (CH 4 ), ethanol (C 2 H 5 OH), and/or monoethylene glycol (OHC 2 H 4 OH). 11 . The reduction process as claimed in claim 10 , further comprising converting the hydroxide ions (OH − ) formed in the carbon dioxide reduction to hydrogencarbonate ions (HCO 3 − ) with carbon dioxide (CO 2 ) present in excess. 12 . The reduction process as claimed in claim 9 , further including introducing at least a portion of the catholyte into a deposition tank, where it is cooled down by at least 15 kelvin. 13 . The reduction process as claimed in claim 9 , further comprising introducing at least a portion of the catholyte volume into a deposition tank, where the pH thereof is lowered from above 8 to a pH of 6 or less by blowing in carbon dioxide (CO 2 ). 14 . The reduction process as claimed in claim 9 , further comprising introducing at least a portion of the catholyte volume into a deposition tank, where an alkali metal hydrogencarbonate is crystallized and is subsequently converted to an alkali metal carbonate by heating.
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