Zinc electrodes for batteries

US9802254B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9802254-B2
Application numberUS-201414501629-A
CountryUS
Kind codeB2
Filing dateSep 30, 2014
Priority dateSep 30, 2014
Publication dateOct 31, 2017
Grant dateOct 31, 2017

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  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

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Abstract

Official abstract text for this publication.

A method of: providing an emulsion having a zinc powder and a liquid phase; drying the emulsion to form a sponge; sintering the sponge in an inert atmosphere to form a sintered sponge; heating the sintered sponge in an oxidizing atmosphere to form an oxidized sponge having zinc oxide on the surface of the oxidized sponge; and heating the oxidized sponge in an inert atmosphere at above the melting point of the zinc. A method of: providing an emulsion comprising a zinc powder and a liquid phase; placing the emulsion into a mold, wherein the emulsion is in contact with a metal substrate; and drying the emulsion to form a sponge.

First claim

Opening claim text (preview).

What is claimed is: 1. A method comprising: providing a mixture comprising a zinc powder and a liquid phase emulsion; drying the emulsion to form a sponge; sintering the sponge in an inert atmosphere to form a sintered sponge; heating the sintered sponge in an oxidizing atmosphere to form an oxidized sponge comprising zinc oxide on the surface of the oxidized sponge; and heating the oxidized sponge in an inert atmosphere at above the melting point of the zinc. 2. The method of claim 1 , wherein the sintering is performed at at least two thirds of the melting point of the zinc and below the melting point of the zinc. 3. The method of claim 1 , wherein heating the sintered sponge is performed at a temperature greater than the melting point of the zinc. 4. The method of claim 1 , wherein heating the oxidized sponge is performed at a temperature greater than the melting point of the zinc. 5. The method of claim 1 , wherein the sintering, heating the sintered sponge, and heating the oxidized sponge are each performed with dwell times of at least 30 minutes. 6. The method of claim 1 , wherein the zinc powder or liquid phase comprises an additive that suppresses gas evolution and corrosion of the sponge. 7. The method of claim 6 , wherein the additive comprises bismuth and indium. 8. The method of claim 1 , wherein the liquid phase emulsion comprises water and decane. 9. The method of claim 1 , wherein the emulsion comprises an emulsifier and an emulsion stabilizer. 10. The method of claim 9 , wherein the emulsifier is sodium dodecyl sulfate and emulsion stabilizer is carboxymethylcellulose. 11. The method of claim 1 , wherein the sintering is performed under argon at a peak temperature of 200-410° C. 12. The method of claim 1 , wherein the heating is performed in air at a peak temperature greater than 420° C. 13. The method of claim 1 , further comprising: electrochemically reducing the zinc oxide to form a zinc metal sponge. 14. The method of claim 13 , wherein the zinc oxide is reduced by applying a negative voltage to the oxidized sponge until the open-circuit potential vs. zinc is less than 5 mV. 15. A method comprising: providing a mixture comprising a zinc powder and a liquid phase emulsion; placing the mixture into a mold, wherein the mixture is in contact with a metal substrate; drying the mixture to form a sponge; removing the mold from the sponge and substrate; sintering the sponge in an inert atmosphere to form a sintered sponge; heating the sintered sponge in an oxidizing atmosphere to form an oxidized sponge comprising zinc oxide on the surface of the oxidized sponge; and heating the oxidized sponge in an inert atmosphere at above the melting point of the zinc. 16. The method of claim 15 , wherein the substrate is a metal mesh. 17. The method of claim 16 , wherein the mesh has an average opening size that is less than the d 50 particle size of the zinc powder. 18. The method of claim 15 , wherein the substrate is a metal foil. 19. The method of claim 15 , wherein the substrate comprises tin or tin-coated copper. 20. The article made by the method of claim 15 . 21. The method of claim 15 , further comprising electrochemically reducing the zinc oxide to form a zinc metal sponge. 22. The article made by the method of claim 21 .

Assignees

Inventors

Classifications

  • B22F3/11Primary

    Making porous workpieces or articles · CPC title

  • After-treatment maintaining the porosity (B22F3/114 takes precedence) · CPC title

  • involving an oxidation, reduction or reaction step · CPC title

  • Physical characteristics, e.g. porosity, surface area · CPC title

  • Processes of manufacture · CPC title

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Frequently asked questions

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What does patent US9802254B2 cover?
A method of: providing an emulsion having a zinc powder and a liquid phase; drying the emulsion to form a sponge; sintering the sponge in an inert atmosphere to form a sintered sponge; heating the sintered sponge in an oxidizing atmosphere to form an oxidized sponge having zinc oxide on the surface of the oxidized sponge; and heating the oxidized sponge in an inert atmosphere at above the melti…
Who is the assignee on this patent?
Rolison Debra R, Parker Joseph F, Long Jeffrey W, and 1 more
What technology area does this patent fall under?
Primary CPC classification B22F3/11. Mapped technology areas include Operations & Transport.
When was this patent published?
Publication date Tue Oct 31 2017 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).