CN102856594A - Power type lead-acid storage battery colloidal electrolyte - Google Patents

Power type lead-acid storage battery colloidal electrolyte Download PDF

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Publication number
CN102856594A
CN102856594A CN201210341591XA CN201210341591A CN102856594A CN 102856594 A CN102856594 A CN 102856594A CN 201210341591X A CN201210341591X A CN 201210341591XA CN 201210341591 A CN201210341591 A CN 201210341591A CN 102856594 A CN102856594 A CN 102856594A
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CN
China
Prior art keywords
sulfuric acid
storage battery
colloidal electrolyte
content
power type
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201210341591XA
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Chinese (zh)
Inventor
王涛
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shandong Sacred Sun Power Sources Co Ltd
Original Assignee
SHANDONG SACRED SUN POWER SUPPLY TECHNOLOGY Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
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Application filed by SHANDONG SACRED SUN POWER SUPPLY TECHNOLOGY Co Ltd filed Critical SHANDONG SACRED SUN POWER SUPPLY TECHNOLOGY Co Ltd
Priority to CN201210341591XA priority Critical patent/CN102856594A/en
Publication of CN102856594A publication Critical patent/CN102856594A/en
Pending legal-status Critical Current

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    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10Energy storage using batteries

Abstract

The invention discloses a power type lead-acid storage battery colloidal electrolyte and relates to storage batteries. Currently, the lead-acid storage batteries at home generally utilize dilute sulfuric acid as electrolyte, the dilute sulfuric acid is adhered on an AGM clapboard by gravity to generate delamination, the sulfuric acid concentration on the lower part of the storage battery polar plate is over high, the anode PbSO4 cannot be completely converted into PbO2 during the charging process, the current on the lower half part of the polar plate away from the pole lug of the polar plate is small to be insufficiently charged to cause sulfuric acid salinization, so that the service life of the storage battery is shortened. The power type lead-acid storage battery colloidal electrolyte is characterized in that the colloidal electrolyte further comprises a thickener and a flocculant, the content of sulfuric acid is 30-50 wt%, the content of sodium sulfate is 0.50-2 wt%, the content of nanometer silicon dioxide is 5-15 wt%, the content of polyacrylamide is 0.1-0.5 wt%, and the balance of deionized water. The power type lead-acid storage battery colloidal electrolyte disclosed by the invention has the beneficial effects of effectively reducing the delamination of the sulfuric acid and prolonging the service life.

Description

A kind of power lead acid battery colloidal electrolyte
Technical field
The present invention relates to storage battery, is a kind of power lead acid battery colloidal electrolyte more specifically.
Background technology
At present, domestic lead acid accumulator adopts dilute sulfuric acid to do electrolyte more, produces layering but gravity causes dilute sulfuric acid to be attached on the AGM dividing plate, and accumulator plate bottom sulfuric acid density is too high, during charging, and anodal PbSO 4Can not change into PbO fully 2, cause pole plate the latter half active material utilization low, pole plate top and the bottom CURRENT DISTRIBUTION is inhomogeneous, and is little away from pole plate the latter half electric current of pole plate lug, and charging owes to fill, and causes sulfation, and the life of storage battery shortens.
Summary of the invention
The purpose of this invention is to provide a kind of power lead acid battery colloidal electrolyte, can overcome the deficiency of sulfuric acid stratification, have the advantages that effectively to reduce sulfuric acid stratification, to increase the service life.
The present invention realizes in the following way: a kind of power lead acid battery colloidal electrolyte, contain deionized water, sulfuric acid, nanometer grade silica, it is characterized in that colloidal electrolyte also contains thickener and flocculant, wherein the content of sulfuric acid is 30~50 (weight) %, the content of sodium sulphate is 0.50~2 (weight) %, nanometer grade silica content is 5~15 (weight) %, and the polyacrylamide amine content is 0.1~0.5 (weight) %, and all the other are deionized water.During operation, with 5~15 (weight) % nanometer grade silica as gel, mix with the sulfuric acid of 45% concentration of 0.50~2 (weight) %, 50 ℃ of lower stirrings 2~8 hours of constant temperature, then the polyacrylamide of 0.1~0.5 (weight) % that acicular nano crystal whisker or acicular nanometer fento is made as the sodium sulphate of flocculant (flow ability modifying agent) and 0.50~2 (weight) % of crystal as thickener (gel reinforcing agent) disperse join before in the mixed solution under 50 ℃, stir 4~8 hours to room temperature, at last ionized water is added in the mixed solution, regulate mixed liquor to 100 (weight) %, can obtain this colloidal electrolyte.
The invention has the beneficial effects as follows: a kind of power lead acid battery colloidal electrolyte of the present invention has the advantage that can effectively reduce sulfuric acid stratification, increase the service life.
Embodiment
During operation, with 5~15 (weight) % nanometer grade silica as gel, mix with the sulfuric acid of 45% concentration of 0.50~2 (weight) % that has prepared, keep stirring 2~8 hours with mixer under 50 ℃ of constant temperature, then the polyacrylamide of 0.1~0.5 (weight) % that acicular nano crystal whisker or acicular nanometer fento is made as the sodium sulphate of flocculant (flow ability modifying agent) and 0.50~2 (weight) % of crystal as thickener (gel reinforcing agent) disperse join before in the mixed solution under 50 ℃ of the constant temperature, stir 4~8 hours to room temperature with mixer, at last ionized water is added in the mixed solution, regulate mixed liquor to 100 (weight) %, can obtain this colloidal electrolyte.

Claims (2)

1. a power lead acid battery colloidal electrolyte contains deionized water, sulfuric acid, nanometer grade silica, it is characterized in that colloidal electrolyte also contains thickener and flocculant.
2. a kind of power lead acid battery colloidal electrolyte as claimed in claim 1, wherein the content of sulfuric acid is 30~50 (weight) %, the content of sodium sulphate is 0.50~2 (weight) %, nanometer grade silica content is 5~15 (weight) %, the polyacrylamide amine content is 0.1~0.5 (weight) %, and all the other are deionized water.
CN201210341591XA 2012-09-04 2012-09-04 Power type lead-acid storage battery colloidal electrolyte Pending CN102856594A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201210341591XA CN102856594A (en) 2012-09-04 2012-09-04 Power type lead-acid storage battery colloidal electrolyte

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201210341591XA CN102856594A (en) 2012-09-04 2012-09-04 Power type lead-acid storage battery colloidal electrolyte

Publications (1)

Publication Number Publication Date
CN102856594A true CN102856594A (en) 2013-01-02

Family

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Family Applications (1)

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CN201210341591XA Pending CN102856594A (en) 2012-09-04 2012-09-04 Power type lead-acid storage battery colloidal electrolyte

Country Status (1)

Country Link
CN (1) CN102856594A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103606710A (en) * 2013-10-30 2014-02-26 山东圣阳电源股份有限公司 Formula of silicon mixing-dissolution colloid electrolyte solution for colloid accumulator and preparation method thereof
CN103972591A (en) * 2014-05-16 2014-08-06 浙江天能电池(江苏)有限公司 Lead-acid storage battery nanometer colloid electrolyte and preparation method thereof
CN104201424A (en) * 2014-08-30 2014-12-10 广东中商国通电子有限公司 Silicon master-batch with super-hydrophilic property, and preparation method of silicon master-batch
CN105529502A (en) * 2014-09-30 2016-04-27 佛山市高明区(中国科学院)新材料专业中心 Gel battery electrolyte

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103606710A (en) * 2013-10-30 2014-02-26 山东圣阳电源股份有限公司 Formula of silicon mixing-dissolution colloid electrolyte solution for colloid accumulator and preparation method thereof
CN103972591A (en) * 2014-05-16 2014-08-06 浙江天能电池(江苏)有限公司 Lead-acid storage battery nanometer colloid electrolyte and preparation method thereof
CN103972591B (en) * 2014-05-16 2016-08-31 浙江天能电池(江苏)有限公司 A kind of lead-acid accumulator nanometer colloid electrolyte and preparation method thereof
CN104201424A (en) * 2014-08-30 2014-12-10 广东中商国通电子有限公司 Silicon master-batch with super-hydrophilic property, and preparation method of silicon master-batch
CN105529502A (en) * 2014-09-30 2016-04-27 佛山市高明区(中国科学院)新材料专业中心 Gel battery electrolyte

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PB01 Publication
TA01 Transfer of patent application right

Effective date of registration: 20140212

Address after: 273100 Shandong province Qufu Shengyang Road No. 1

Applicant after: Shandong Sacred Sun Power Sources Co., Ltd.

Address before: 273100 No. 6, customs East Road, Qufu, Shandong

Applicant before: Shandong Sacred Sun Power Supply Technology Co., Ltd.

TA01 Transfer of patent application right
C02 Deemed withdrawal of patent application after publication (patent law 2001)
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20130102