Lead-acid battery

Patent metadata

Field	Value
Publication number	US-9553335-B2
Application number	US-201013996680-A
Country	US
Kind code	B2
Filing date	Dec 21, 2010
Priority date	Dec 21, 2010
Publication date	Jan 24, 2017
Grant date	Jan 24, 2017

Abstract

A lead-acid battery improving the charge acceptance in an initial stage, suppressing the decrease of the charge acceptance for a long time use of the battery and having a long life is provided. In a lead-acid battery using a paste type negative plate prepared by filling a past form negative active material using a lead powder as a starting material in a collector made of a lead alloy, a flake graphite and a condensate of bisphenols and aminobenzene sulfonic acid are contained in the negative active material. The average primary particle diameter of the flake graphite is 10 μm or more and 220 μm or less, preferably, 100 μm or more and 220 μm or less. The content of the flake graphite is preferably from 0.5 mass parts to 2.7 mass parts and, more preferably, from 1.1 mass parts to 2.2 mass parts based on 100 mass parts of the negative active material (spongy metallic lead) in a fully charged state.

First claim

The invention claimed is:

1. A lead-acid battery having a configuration in which a group of plates formed by stacking negative plates where a negative active material is filled in a negative collector and positive plates where a positive active material is filled in a positive collector by way of a separator is contained together with an electrolyte in a container, wherein
the negative active material contains a flake graphite and a condensate of bisphenols and aminobenzene sulfonic acid in the negative active material, and
the average primary particle diameter of the flake graphite is 100 μm or more and 220 μm or less.

2. The lead-acid battery according to claim 1 , wherein the negative active material further contains spongy metallic lead, and the content of the flake graphite in the negative active material is from 0.5 mass % to 2.7 mass % of the flake graphite based on 100 mass parts of the spongy metallic lead in the negative active material in a fully charged state.

3. The lead-acid battery according to claim 1 , wherein the negative active material further contains spongy metallic lead, and the content of the flake graphite in the negative active material is from 1.1 mass % to 2.2 mass % of the flake graphite based on 100 mass parts of the spongy metallic lead in the negative active material in a fully charged state.

4. The lead-acid battery according to claim 1 , wherein the condensate of the bisphenols and aminobenzene sulfonic acid is a formaldehyde condensate of bisphenol A and sodium aminobenzene sulfonate represented by the following chemical structural formula [chem. 1]

R 1 and R 2 represent each hydrogen or

(excluding a case where both R 1 and R 2 are hydrogen).

5. The lead-acid battery according to claim 1 , wherein the separator is formed of a non-woven fabric comprising at least one fiber material selected from the group of materials consisting of glass, pulp, and polyolefin.

6. The lead-acid battery according to claim 1 , wherein the surface of the separator opposed to the surface of the negative plate is formed of a non-woven fabric comprising at least one fiber material selected from the group of materials consisting of glass, pulp and polyolefin, and the surface thereof opposed to the surface of the positive plate is formed of a porous polyethylene sheet.

7. The lead-acid battery according to claim 1 , wherein the average primary particle diameter of the flake graphite is 140 μm or more and 220 μm or less.

8. A lead-acid battery having a configuration in which a group of plates formed by stacking negative plates where a negative active material is filled in a negative collector and positive plates where a positive active material is filled in a positive collector by way of a separator is contained together with an electrolyte in a container, wherein
the negative active material contains spongy metallic lead, a flake graphite, and a condensate of bisphenols and aminobenzene sulfonic acid in the negative active material,
the average primary particle diameter of the flake graphite is 100 μm or more and 220 μm or less, and
the content of the flake graphite in the negative active material is from 0.5 mass % to 2.2 mass % of the flake graphite based on 100 mass parts of the spongy metallic lead in the negative active material in a fully charged state.

9. The lead-acid battery according to claim 8 , wherein the condensate of the bisphenols and aminobenzene sulfonic acid is a formaldehyde condensate of bisphenol A and sodium aminobenzene sulfonate represented by the following chemical structural formula [chem. 1]

R 1 and R 2 represent each hydrogen or

(excluding a case where both R 1 and R 2 are hydrogen).

10. The lead-acid battery according to claim 9 , wherein the surface of the separator opposed to the surface of the negative plate is formed of a non-woven fabric comprising at least one fiber material selected from the group of materials consisting of glass, pulp, and polyolefin.

11. The lead-acid battery according to claim 8 , wherein the average primary particle diameter of the flake graphite is 140 μm or more and 220 μm or less.

12. A lead-acid battery comprising:
negative plates including negative collectors filled with a negative active material;
positive plates including positive collectors filled with a positive active material, wherein the negative plates are alternately stacked with the positive plates;
separators between the negative plates and the positive plates;
an electrolyte; and
a container holding the negative plates, the positive plates, and the electrolyte,
wherein the negative active material contains a flake graphite and a condensate of bisphenols and aminobenzene sulfonic acid, and the average primary particle diameter of the flake graphite is 100 μm or more and 220 μm or less.

13. The lead-acid battery according to claim 12 , wherein the average primary particle diameter of the flake graphite is 140 μm or more and 220 μm or less.

Assignees

• Kogure Koji
• Toduka Masatoshi
• Hitachi Chemical Co Ltd

Inventors

• Kogure Koji
• Toduka Masatoshi

Classifications

• H01M4/606

  containing aromatic main chain polymers · CPC title

• H01M4/583 Primary

  Carbonaceous material, e.g. graphite-intercalation compounds or CFx · CPC title

• H01M50/409

  Separators, membranes or diaphragms characterised by the material · CPC title

• H01M50/417

  Polyolefins · CPC title

• H01M50/44

  Fibrous material · CPC title