US2018195184A1PendingUtilityA1

Electrolytic System And Reduction Method For Electrochemical Carbon Dioxide Utilization, Alkali Carbonate Preparation And Alkali Hydrogen Carbonate Preparation

Assignee: SIEMENS AGPriority: Jul 3, 2015Filed: Jul 30, 2016Published: Jul 12, 2018
Est. expiryJul 3, 2035(~8.9 yrs left)· nominal 20-yr term from priority
C25B 1/01C25B 3/07C25B 3/03C25B 15/083C25B 3/26C25B 1/23C25B 15/08C25B 3/04C25B 1/14C25B 15/087C25B 1/26C25B 3/25C25B 1/00
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Claims

Abstract

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.

Claims

exact text as granted — not AI-modified
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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