Process and high surface area electrodes for the electrochemical reduction of carbon dioxide

US10287696B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10287696-B2
Application numberUS-201414471152-A
CountryUS
Kind codeB2
Filing dateAug 28, 2014
Priority dateJul 26, 2012
Publication dateMay 14, 2019
Grant dateMay 14, 2019

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

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Methods and systems for electrochemical conversion of carbon dioxide to organic products including formate and formic acid are provided. A method may include, but is not limited to, steps (A) to (C). Step (A) may introduce an acidic anolyte to a first compartment of an electrochemical cell. The first compartment may include an anode. Step (B) may introduce a bicarbonate-based catholyte saturated with carbon dioxide to a second compartment of the electrochemical cell. The second compartment may include a high surface area cathode including indium and having a void volume of between about 30% to 98%. At least a portion of the bicarbonate-based catholyte is recycled. Step (C) may apply an electrical potential between the anode and the cathode sufficient to reduce the carbon dioxide to at least one of a single-carbon based product or a multi-carbon based product.

First claim

Opening claim text (preview).

What is claimed is: 1. A method for electrochemical reduction of carbon dioxide into products, comprising: (A) introducing an acidic anolyte to a first compartment of a first electrochemical cell, the first compartment including an anode; (B) introducing a catholyte including an alkali metal bicarbonate to a second compartment of the first electrochemical cell, the catholyte saturated with carbon dioxide, the second compartment including a high surface area cathode, the high surface area cathode including a coating containing indium and having a void volume of between about 30% to 98%, at least a portion of the catholyte including the alkali metal bicarbonate being recycled; (C) applying an electrical potential between the anode and the cathode sufficient to reduce the carbon dioxide to an alkali metal formate; (D) introducing the alkali metal formate to an ion exchange compartment of a second electrochemical cell; (E) applying an electrical potential between an anode of the second electrochemical cell and a cathode of the second electrochemical cell sufficient to produce at least formic acid and an alkali metal hydroxide; (F) introducing the alkali metal hydroxide with carbon dioxide to generate at least a portion of the alkali metal bicarbonate introduced to the second compartment of the first electrochemical cell; and (G) separating the alkali metal formate from the alkali metal bicarbonate of the catholyte of the first electrochemical cell with a nano-filtration system, wherein the nano-filtration system separates monovalent anions from divalent anions. 2. The method of claim 1 , wherein separating the alkali metal formate from the alkali metal bicarbonate of the catholyte of the first electrochemical cell with a nano-filtration system comprises: introducing the alkali metal bicarbonate of the catholyte to an alkali metal hydroxide to convert at least a portion of the alkali metal bicarbonate to an alkali metal carbonate; and separating the alkali metal carbonate from the alkali metal formate with a nano-filtration unit. 3. The method of claim 2 , further comprising: introducing the alkali metal carbonate with the alkali metal hydroxide and with carbon dioxide to generate at least a portion of the alkali metal bicarbonate introduced to the second compartment of the first electrochemical cell. 4. The method of claim 1 , wherein at least a portion of the alkali metal hydroxide is generated by one or more of the first electrochemical cell and the second electrochemical cell. 5. The method of claim 1 , wherein the formic acid is generated in the ion exchange compartment of the second electrochemical cell. 6. The method of claim 1 , wherein the alkali metal hydroxide is generated in a cathode compartment of the second electrochemical cell. 7. The method of claim 1 , wherein the high surface area cathode has a specific surface area of greater than 2 cm 2 /cm 3 . 8. The method of claim 1 , wherein the acidic anolyte includes sulfuric acid. 9. The method of claim 1 , further comprising: generating a halogen selected from the group consisting of F 2 , Cl 2 , Br 2 , and I 2 in at least one of the first compartment of the first electrochemical cell and the first compartment of the second electrochemical cell. 10. The method of claim 9 , further comprising: reacting the halogen with an organic compound to produce a halogenated product. 11. The method of claim 10 , wherein the halogen is bromine. 12. The method of claim 9 , wherein the halogen is bromine. 13. The method of claim 1 , wherein the high surface area cathode includes from 5% to 99% as indium in alloy with bismuth.

Assignees

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Classifications

  • Operating or servicing cells · CPC title

  • Chemistry & Metallurgy · mapped topic

  • Chemistry & Metallurgy · mapped topic

  • C25B15/08Primary

    Supplying or removing reactants or electrolytes; Regeneration of electrolytes · CPC title

  • Chemistry & Metallurgy · mapped topic

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What does patent US10287696B2 cover?
Methods and systems for electrochemical conversion of carbon dioxide to organic products including formate and formic acid are provided. A method may include, but is not limited to, steps (A) to (C). Step (A) may introduce an acidic anolyte to a first compartment of an electrochemical cell. The first compartment may include an anode. Step (B) may introduce a bicarbonate-based catholyte saturate…
Who is the assignee on this patent?
Liquid Light Inc, Avantium Knowledge Centre Bv
What technology area does this patent fall under?
Primary CPC classification C25B15/08. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue May 14 2019 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).