Lead-acid battery

US12463221B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-12463221-B2
Application numberUS-202017614885-A
CountryUS
Kind codeB2
Filing dateMay 29, 2020
Priority dateMay 31, 2019
Publication dateNov 4, 2025
Grant dateNov 4, 2025

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  1. Title

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  2. Abstract

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  4. Key dates

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  5. First independent claim

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Abstract

Official abstract text for this publication.

A lead-acid battery includes a positive electrode plate, a negative electrode plate, and an electrolyte solution. The negative electrode plate includes a negative electrode material. The negative electrode material contains a polymer compound. The polymer compound has a peak in a range of 3.2 ppm or more and 3.8 ppm or less in a chemical shift of 1 H-NMR spectrum, or the negative electrode material contains a polymer compound having a repeating structure of oxy C 2-4 alkylene units.

First claim

Opening claim text (preview).

The invention claimed is: 1 . A lead-acid battery comprising a positive electrode plate, a negative electrode plate, and an electrolyte solution, wherein the negative electrode plate comprises a negative electrode material, the negative electrode material contains a polymer compound, the polymer compound has a peak in a range of 3.2 ppm or more and 3.8 ppm or less in a chemical shift of 1 H-NMR spectrum, the polymer compound contains at least one selected from the group consisting of an etherified product of a hydroxy compound having a repeating structure of oxy C 2-4 alkylene units and an esterified product of a hydroxy compound having the repeating structure of the oxy C 2-4 alkylene units, the hydroxy compound is at least one selected from the group consisting of a poly C 2-4 alkylene glycol, a copolymer having a repeating structure of oxy C 2-4 alkylene, and a C 2-4 alkylene oxide adduct of a polyol, the negative electrode material further contains an organic expander, a content of the polymer compound in the negative electrode material is 16 ppm or more and 350 ppm or less on a mass basis, and a number average molecular weight of the polymer compound is 1,000 or more and 5,000 or less. 2 . The lead-acid battery according to claim 1 , wherein the content of the polymer compound in the negative electrode material is 16 ppm or more and 200 ppm or less on a mass basis. 3 . The lead-acid battery according to claim 1 , wherein the polymer compound contains an oxygen atom bonded to a terminal group and a —CH 2 — group and/or a —CH< group bonded to the oxygen atom, and in the 1 H-NMR spectrum, a ratio of an integrated value of the peak to a sum of the integrated value of the peak, an integrated value of a peak of a hydrogen atom of the —CH 2 — group, and an integrated value of a peak of a hydrogen atom of the —CH< group is 85% or more. 4 . The lead-acid battery according to claim 1 , wherein the repeating structure of the oxy C 2-4 alkylene units contains at least a repeating structure of oxypropylene units. 5 . The lead-acid battery according to claim 1 , wherein the electrolyte solution contains the polymer compound, and the concentration of the polymer compound in the electrolyte solution is 500 ppm or less on a mass basis. 6 . The lead-acid battery according to claim 1 , wherein the electrolyte solution contains the polymer compound, and the concentration of the polymer compound in the electrolyte solution is 100 ppm or more on a mass basis. 7 . The lead-acid battery according to claim 1 , wherein the organic expander contains a first organic expander having a sulfur element content of 2,000 μmol/g or more. 8 . The lead-acid battery according to claim 7 , wherein the first organic expander contains a condensate containing a unit of an aromatic compound having a sulfur-containing group, and the condensate contains, as the unit of the aromatic compound, at least one selected from the group consisting of a unit of a bisarene compound and a unit of a monocyclic aromatic compound. 9 . The lead-acid battery according to claim 8 , wherein the condensate contains the unit of the bisarene compound and the unit of the monocyclic aromatic compound. 10 . The lead-acid battery according to claim 8 , wherein the unit of the monocyclic aromatic compound includes a unit of a hydroxyarene compound. 11 . The lead-acid battery according to claim 1 , wherein the organic expander contains a second organic expander having a sulfur element content of less than 2,000 μmol/g. 12 . The lead-acid battery according to claim 1 , wherein the polymer compound is one selected from a group consisting of polypropylene glycol, polyoxyethylene polyoxypropylene butyl ether, polyoxypropylene butyl ether, polyoxypropylene methyl ether, polyoxypropylene ethyl ether and polyoxypropylene acetate. 13 . A lead-acid battery comprising a positive electrode plate, a negative electrode plate, and an electrolyte solution, wherein the negative electrode plate comprises a negative electrode material, the negative electrode material contains a polymer compound having a repeating structure of oxy C 2-4 alkylene units, the polymer compound contains at least one selected from the group consisting of an etherified product of a hydroxy compound having a repeating structure of oxy C 2-4 alkylene units and an esterified product of a hydroxy compound having the repeating structure of the oxy C 2-4 alkylene units, the hydroxy compound is at least one selected from the group consisting of a poly C 2-4 alkylene glycol, a copolymer having a repeating structure of oxy C 2-4 alkylene, and a C 2-4 alkylene oxide adduct of a polyol, the negative electrode material further contains an organic expander, a content of the polymer compound in the negative electrode material is 16 ppm or more and 350 ppm or less on a mass basis, and a number average molecular weight of the polymer compound is 1,000 or more and 5,000 or less. 14 . The lead-acid battery according to claim 13 , wherein the content of the polymer compound in the negative electrode material is 16 ppm or more and 200 ppm or less on a mass basis. 15 . The lead-acid battery according to claim 13 , wherein the polymer compound contains an oxygen atom bonded to a terminal group and a —CH 2 — group and/or a —CH< group bonded to the oxygen atom, and in the 1 H-NMR spectrum, a ratio of an integrated value of the peak to a sum of the integrated value of the peak, an integrated value of a peak of a hydrogen atom of the —CH 2 — group, and an integrated value of a peak of a hydrogen atom of the —CH< group is 85% or more.

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What does patent US12463221B2 cover?
A lead-acid battery includes a positive electrode plate, a negative electrode plate, and an electrolyte solution. The negative electrode plate includes a negative electrode material. The negative electrode material contains a polymer compound. The polymer compound has a peak in a range of 3.2 ppm or more and 3.8 ppm or less in a chemical shift of 1 H-NMR spectrum, or the negative electrode mat…
Who is the assignee on this patent?
Gs Yuasa Int Ltd
What technology area does this patent fall under?
Primary CPC classification H01M10/06. Mapped technology areas include Electricity.
When was this patent published?
Publication date Tue Nov 04 2025 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 2 related publications on this page (citations in our corpus or others sharing the same primary CPC).