Enhanced electrochemical oxidation of carbonaceous deposits in liquid-hydrocarbon fueled solid oxide fuel cells

US10056635B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10056635-B2
Application numberUS-201514623884-A
CountryUS
Kind codeB2
Filing dateFeb 17, 2015
Priority dateFeb 17, 2015
Publication dateAug 21, 2018
Grant dateAug 21, 2018

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  5. First independent claim

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Abstract

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Embodiments of a method of removing carbonaceous deposits in a liquid-hydrocarbon fueled solid oxide fuel cell and related system are provided. The method includes providing a solid oxide fuel cell system having an anode, a cathode, a solid oxide electrolyte oriented between the anode and cathode, an amplifier cathode disposed proximate the solid oxide electrolyte and the cathode, a fuel cell electric circuit electrically connecting the anode and the cathode, and an amplifier electric circuit electrically connecting the anode and the amplifier cathode. Further, operating the amplifier electric circuit in an electrolytic mode to electrically power the amplifier cathode, wherein the amplifier cathode generates and supplies O 2− or CO 3 2− to the anode. The method further includes removing the carbonaceous deposits on the anode by converting the carbonaceous deposits to carbon dioxide gas via reaction with the O 2− or CO 3 2− and expelling the carbon dioxide gas.

First claim

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What is claimed is: 1. A method of removing carbonaceous deposits in a liquid-hydrocarbon fueled solid oxide fuel cell, the method comprising: providing a solid oxide fuel cell system comprising an anode, a cathode, a solid oxide electrolyte oriented between the anode and cathode, an amplifier cathode disposed proximate the solid oxide electrolyte and the cathode, a fuel cell electric circuit electrically connecting the anode and the cathode, and an amplifier electric circuit electrically connecting the anode and the amplifier cathode, wherein the amplifier electric circuit comprises at least one battery, potentiostat, or galvanostat that powers and controls the amplifier electric circuit; operating the amplifier electric circuit in an electrolytic mode to electrically power the amplifier cathode, wherein the amplifier cathode generates and supplies O 2− or CO 3 2− to the anode; and removing the carbonaceous deposits on the anode by converting the carbonaceous deposits to carbon dioxide gas via reaction with the O 2− or CO 3 2− and expelling the carbon dioxide gas. 2. The method of claim 1 , wherein the current supplied to the amplifier electric circuit is substantially constant over time. 3. The method of claim 2 , wherein the current supplied to the amplifier electric circuit maintains a voltage above the O 2 reduction potential and below the electrolyte reduction potential. 4. The method of claim 1 , wherein the current supplied to the amplifier electrode circuit is pulsed. 5. The method of claim 4 , wherein the solid oxide fuel cell system further comprises a control circuit to pulse the current supplied to the amplifier electrode circuit such that current is supplied when the power output of the solid oxide fuel cell system drops below 50% of initial operation without carbonaceous deposits. 6. The method of claim 1 , wherein the cathode and the amplifier cathode are different compositions. 7. The method of claim 1 , wherein the cathode, the amplifier cathode, or both is selected from the group consisting of at least one perovskite material of the general type ABO 3 or ABMO 3 or A 1-x Sr x Fe 1-y Co y O 3-δ or A 1-x B x M 1-y Mg y O 3-δ , wherein: A is La, Sn, Nd, Gd, Ba or Dy, B is a 2 + , 3 + , 4 + or 5 + cation, and M is a transition metal. 8. The method of claim 7 , wherein the perovskite material is LaSrFeCoO 3-δ (LSCF), or LaSrMnO 3-δ (LSM), or Sr 2 MgMo 0.8 Nb 0.2 O 6-δ . 9. The method of claim 1 , wherein the anode comprises a metallic, metal oxide, or ceramic-metallic. 10. The method of claim 9 , wherein the anode comprises metal selected from the group consisting of iron (Fe), copper (Cu), nickel (Ni), cobalt (Co), molybdenum (Mo), gold (Au), ruthenium (Ru), rhodium (Rh), tungsten (W), chromium (Cr), terbium (Tb), magnesium (Mg), platinum (Pt), palladium (Pd), and combinations thereof. 11. The method of claim 1 , wherein the electrolyte is zirconia-based, ceria-based, titania-based, a perovskite oxide, or cationic carbonate-based. 12. The method of claim 1 , wherein the solid oxide fuel cell system further comprises a liquid fuel atomizer located to distribute the liquid-hydrocarbon fuel across the anode. 13. A method of removing carbonaceous deposits in a liquid-hydrocarbon fueled solid oxide fuel cell, the method comprising: providing a solid oxide fuel cell system comprising an anode, a cathode, a solid oxide electrolyte oriented between the anode and cathode, an amplifier cathode disposed proximate the solid oxide electrolyte and the cathode, a fuel cell electric circuit electrically connecting the anode and the cathode, and an amplifier electric circuit comprising at least one battery, potentiostat, or galvanostat electrically connecting the anode and the amplifier cathode; monitoring a power reaction speed of the solid oxide fuel cell system; operating the amplifier electric circuit in an electrolytic mode to electrically power the amplifier cathode, wherein the amplifier cathode generates and supplies O 2− or CO 3 2− to the anode; removing the carbonaceous deposits on the anode by converting the carbonaceous deposits to carbon dioxide gas via reaction with the O 2− or CO 3 2− and expelling the carbon dioxide gas; and adjusting the current supplied to the amplifier electric circuit to obtain steady-state operation of the removal of the carbonaceous deposits on the anode. 14. The method of claim 13 , wherein the current supplied to the amplifier electric circuit is substantially constant over time. 15. The method of claim 13 , wherein the current supplied to the amplifier electrode circuit is pulsed. 16. The method of claim 13 , wherein the amplifier electric circuit further comprises at least one potentiostat that powers and controls the amplifier electric circuit. 17. The method of claim 13 , wherein the amplifier electric circuit further comprises at least one galvanostat that powers and controls the amplifier electric circuit. 18. The method of claim 11 , wherein the zirconia-based electrolytes are selected from the group consisting of yttria stabilized ZrO 2 (YSZ), scandia stabilized ZrO 2 (ScSZ), calcia stabilized ZrO 2 (CSZ), samaria stabilized ZrO 2 (SmSZ), and combinations thereof. 19. The method of claim 11 , wherein the ceria-based electrolytes are selected from the group consisting of gadolinium doped ceria (GDC), yttria doped ceria (YDC), samarium doped ceria (SmDC), scandium doped ceria (GDC), zirconium doped ceria (ZDC), gadolinia stabilized ceria (CGO) and combinations thereof.

Assignees

Inventors

Classifications

  • H01M8/0656Primary

    by electrochemical means (H01M8/065 takes precedence) · CPC title

  • the electrolyte consisting of oxides · CPC title

  • Fuel cells with solid oxide electrolytes · CPC title

  • Oxides · CPC title

  • operating at high temperature, e.g. with stabilised ZrO2 electrolyte · CPC title

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What does patent US10056635B2 cover?
Embodiments of a method of removing carbonaceous deposits in a liquid-hydrocarbon fueled solid oxide fuel cell and related system are provided. The method includes providing a solid oxide fuel cell system having an anode, a cathode, a solid oxide electrolyte oriented between the anode and cathode, an amplifier cathode disposed proximate the solid oxide electrolyte and the cathode, a fuel cell e…
Who is the assignee on this patent?
Saudi Arabian Oil Co
What technology area does this patent fall under?
Primary CPC classification H01M8/0656. Mapped technology areas include Electricity.
When was this patent published?
Publication date Tue Aug 21 2018 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 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).