CN104300179A - Container formation process for valve-regulated lead storage battery - Google Patents
Container formation process for valve-regulated lead storage battery Download PDFInfo
- Publication number
- CN104300179A CN104300179A CN201310294296.8A CN201310294296A CN104300179A CN 104300179 A CN104300179 A CN 104300179A CN 201310294296 A CN201310294296 A CN 201310294296A CN 104300179 A CN104300179 A CN 104300179A
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- Prior art keywords
- battery
- acid
- formation process
- valve
- regulated lead
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/06—Lead-acid accumulators
- H01M10/12—Construction or manufacture
- H01M10/121—Valve regulated lead acid batteries [VRLA]
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
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- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Battery Electrode And Active Subsutance (AREA)
- Secondary Cells (AREA)
Abstract
The invention discloses a container formation process for a valve-regulated lead storage battery. The container formation process comprises the steps of battery acidifying, forming and matching. Dilute sulfuric acid with adensity of 1.24-1.26g/cu.cm. at 25 DEG.C is quantitatively added in the battery, wherein the concentrated sulfuric acid content is 31%-33%, the anhydrous sodium sulfate content is 0.8%-1.5%, the stannous sulfate content is 0.1%-0.15%, and the rest is pure water. Each unit cell of each valve-regulated lead storage battery semi-finished product is quantitatively acidified twice; the active substances in the battery are fast and sufficiently transformed through an advanced formation process; compared with the traditional container formation process, the formation time is shortened by 40% and more, the charging amount is reduced by 20% and more, the battery matching rate is improved by 5% and more, and the cycle life of the battery is improved by 20% and more. The container formation process disclosed by the invention further has an advantage that the acid extraction process in the tradition production process is cancelled, so that the uniformity of the battery is improved, the labor consumption is reduced, and the production cost is lowered.
Description
Technical field
The present invention relates to a kind of container formation technique, be specially a kind of valve-regulated lead-acid battery internal formation process.
Background technology
Lead accumulator mainly contains battery case, positive plate, negative plate, dividing plate and electrolyte composition.Pole plate have green plate and ripe pole plate point, changed into by charging in customizations grooving, the lead sulfate in pole plate is changed into the active material that can provide electric energy, such pole plate is exactly ripe pole plate.Adopt the semi-finished product battery of green plate assembling, need to add dilute sulfuric acid and carry out charging and change into, Here it is internal formation process.At present, the production of valve-regulated lead-acid battery mostly adopts internal formation process.Conventional internal formation process adopts the pattern of three chargings and twice electric discharge usually, the online charging interval is long, take circulation material many, charge volume is large simultaneously, the decline space that overall manufacturing cost is very large, therefore, the internal formation process of employing science can shorten the production cycle, reduce production cost, improve Business Economic Benefit, be of great immediate significance.。
Summary of the invention
Technical problem solved by the invention is to provide a kind of valve-regulated lead-acid battery internal formation process, to solve the problem in above-mentioned background technology.
Technical problem solved by the invention realizes by the following technical solutions: a kind of valve-regulated lead-acid battery internal formation process, comprises the following steps:
(1), battery acid adding: whole acid adding process be divided into twice, amount error ± 0.5% of each acid adding.Acid adding amount is 80% ~ 90% of total acid adding amount first, is then transferred to by battery electrode foil chemical reaction shelf carries out charging to change into; Residual acid amount adds in the pilot process changed into.
(2), change into: having of whole formation process is discharged for three times and four chargings, and the online discharge and recharge time is 50h ~ 60h, and total charge volume is 8 ~ 9 times of battery rated capacity.
(3), combo: in order to stable cell quality, improve the useful life of whole Battery pack, after Battery formation terminates, close to the open circuit voltage of every battery, discharge time and closed circuit voltage three key element conditions three or many batteries are formed a group.
The acid of the middle use of described battery acid adding is: dilute sulfuric acid density 1.24 ~ 1.26g/cm
3(25 DEG C), wherein concentrated sulfuric acid content 31% ~ 33% (wt), anhydrous slufuric acid sodium content 0.8% ~ 1.5% (wt), stannous sulfate content 0.1% ~ 0.15% (wt), is adjusted to 1.24 ~ 1.26g/cm with deionized water density
3.
beneficial effect: the present invention makes Battery formation change into time shorten more than 40%, and charge volume reduces more than 20%, and battery combo rate improves more than 5%, and battery cycle life improves more than 20%, and eliminate simultaneously and take out sour technique after changing into, production cost has decline by a relatively large margin.
Embodiment
Reaching object to make technological means of the present invention, creation characteristic, workflow, using method and effect is easy to understand, setting forth the present invention further below.
A kind of valve-regulated lead-acid battery internal formation process, comprises the following steps:
(1), battery acid adding: whole acid adding process be divided into twice, amount error ± 0.5% of each acid adding.Acid adding amount is 80% ~ 90% of total acid adding amount first, is then transferred to by battery electrode foil chemical reaction shelf carries out charging to change into; Residual acid amount adds in the pilot process changed into; Adopt quantitative acid dosing, be in order to cancel change into the later stage take out sour technique, reduce artificial, reduce production cost.
(2), change into: having of whole formation process is discharged for three times and four chargings, and the online discharge and recharge time only has 50h ~ 60h, and total charge volume is 8 ~ 9 times of battery rated capacity.
In theory, the active material that negative pole changes into is velvet-like lead sponge, and be a kind of conductor, resistance is little, and the active material that positive pole transforms is brown lead oxide, and be semiconductor, resistance is large.Facts have proved, when negative electrode active material is fully transformed, positive active material has only transformed about 80%.Change into if continue to charge the battery, just certainly will cause negative electrode active material overcharge, the reaction of the brine electrolysis that simultaneously produces is more violent, the air scour dividing plate that reaction produces and pole plate, the serious curtailment life-span of battery.Therefore, design battery first acid adding amount only has 80% ~ 90% of total acid content, allows battery have one section of lean solution state in the middle and later periods changed into.In this stage, the oxygen that brine electrolysis produces arrives negative terminal surface by dividing plate micropore, and produce chemical reaction with the active material lead of negative pole, produce lead oxide, lead oxide is sulfuric acid reaction, regenerates lead sulfate.The one part of current now acting on negative pole can be reduced into lead sponge lead sulfate.After circulation like this, positive active material transforms fully, and the electric current acted on negative pole is because shunting one part of current is for oxygen cycle, and the electric current being directly used in brine electrolysis diminishes, and just diminishes to the injury that battery causes.
Having of whole formation process is discharged for three times and four chargings, and be convenient to the conversion of active material, the online discharge and recharge time only has 50h ~ 60h, and total charge volume reaches 8 ~ 9 times of battery rated capacity.
(3), combo: in order to stable cell quality, improve the useful life of whole Battery pack, after Battery formation terminates, close to the open circuit voltage of every battery, discharge time and closed circuit voltage three key element conditions three or many batteries are formed a group.
The acid of the middle use of described battery acid adding is: dilute sulfuric acid density 1.24 ~ 1.26g/cm
3(25 DEG C), wherein concentrated sulfuric acid content 31% ~ 33% (wt), anhydrous slufuric acid sodium content 0.8% ~ 1.5% (wt), stannous sulfate content 0.1% ~ 0.15% (wt), all the other are adjusted to 1.24 ~ 1.26g/cm with deionized water density
3.
embodiment 1
1, dilute sulfuric acid density 1.25 g/cm
3(25 DEG C), wherein concentrated sulfuric acid degree 32% (wt), anhydrous sodium sulfate degree 1.1% (wt), stannous sulfate degree 0.1% (wt), all the other are deionized water.
2, total joining in battery of acid adding amount of 88% gone with acid adding machine, acid adding precision controlling is ± 0.5%.
3, leave standstill 1 ~ 3h after battery acid adding, put on charging rack.Charging rack is provided with tank, controls battery temperature with recirculated water.
4, change into, charging current is 0.05C, refers to that electric current is 0.05 times of this battery rated capacity.
First stage charges, and: constant current 0.05C (A) charges 2h;
Second stage is charged, and: constant current 0.3C (A) charges 8h;
Phase III charges, and: constant current 0.2C (A) charges 5h;
First stage discharges, and: constant current 0.3C (A) discharges 1.5h;
Fourth stage is charged, and: constant current 0.3C (A) charges 5h;
Second stage is discharged, and: constant current 0.3C (A) discharges 1.5h;
Five-stage charges, and: constant current 0.3C (A) charges 4h;
6th stage charging: constant current 0.2C (A) charges 8h (this stage terminate after, the acid amount of residue 12% is added district in battery);
7th stage charging: constant current 0.15C (A) charges 4h;
Phase III discharges, and: constant current 0.5C (A) discharges 2.1h;
8th stage charging: constant current 0.3C (A) charges 4h;
9th stage charging: constant current 0.2C (A) charges 2h;
Tenth stage charging: constant current 0.1C (A) charges 6h.
Amount to: total discharge and recharge time 53.1h, total charge volume 102.6Ah.
5, battery combo
By the open circuit voltage only measuring every battery, simultaneously according to the last discharge time in formation process and every battery final voltage, by difference in open circuit voltage be no more than 0.02V, discharge time standard that is consistent, the poor 0.2V of being no more than of final voltage be made into three or many batteries use as one group, the useful life of whole Battery pack can be improved.
More than show and describe general principle of the present invention, principal character and advantage of the present invention.The technical staff of the industry should understand; the present invention is not restricted to the described embodiments; what describe in above-described embodiment and specification just illustrates principle of the present invention; without departing from the spirit and scope of the present invention; the present invention also has various changes and modifications, and these changes and improvements all fall in the claimed scope of the invention.Claimed scope of the present invention is defined by appending claims and equivalent thereof.
Claims (2)
1. a valve-regulated lead-acid battery internal formation process, is characterized in that: a kind of valve-regulated lead-acid battery internal formation process comprises the following steps:
(1), battery acid adding: whole acid adding process be divided into twice, amount error ± 0.5% of each acid adding, acid adding amount is 80% ~ 90% of total acid adding amount first, is then transferred to by battery electrode foil chemical reaction shelf carries out charging to change into; Residual acid amount adds in the pilot process changed into;
(2), change into: having of whole formation process is discharged for three times and four chargings, and the online discharge and recharge time is 50h ~ 60h, and total charge volume is 8 ~ 9 times of battery rated capacity;
(3), combo: in order to stable cell quality, improve the useful life of whole Battery pack, after Battery formation terminates, close to the open circuit voltage of every battery, discharge time and closed circuit voltage three key element conditions three or many batteries are formed a group.
2. a kind of valve-regulated lead-acid battery internal formation process according to claim 1, is characterized in that: the acid of the middle use of described battery acid adding is: dilute sulfuric acid density 1.24 ~ 1.26g/cm
3(25 DEG C), wherein concentrated sulfuric acid content 31% ~ 33% (wt), anhydrous slufuric acid sodium content 0.8% ~ 1.5% (wt), stannous sulfate content 0.1% ~ 0.15% (wt), is adjusted to 1.24 ~ 1.26g/cm with deionized water density
3.
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CN201310294296.8A CN104300179A (en) | 2013-07-15 | 2013-07-15 | Container formation process for valve-regulated lead storage battery |
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107492682A (en) * | 2016-06-13 | 2017-12-19 | 深圳市雄韬电源科技股份有限公司 | Lead-acid accumulator is without recirculated cooling water internal formation process |
CN107681204A (en) * | 2017-09-01 | 2018-02-09 | 超威电源有限公司 | The chemical synthesis technology of the battery prepared using recovery lead powder |
CN109148815A (en) * | 2018-07-18 | 2019-01-04 | 天能电池集团有限公司 | A kind of long-life lead storage battery acid adding chemical synthesizing method |
CN110504495A (en) * | 2019-08-12 | 2019-11-26 | 天能电池集团股份有限公司 | A kind of acid adding chemical synthesizing method of battery |
CN111416164A (en) * | 2020-03-05 | 2020-07-14 | 天能电池集团股份有限公司 | Storage battery container formation and matching method |
CN111600085A (en) * | 2020-01-19 | 2020-08-28 | 超威电源集团有限公司 | Method for manufacturing lead-acid storage battery |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101901935A (en) * | 2010-07-02 | 2010-12-01 | 超威电源有限公司 | Internal formation process for high-capacity gel battery |
CN102593533A (en) * | 2012-03-15 | 2012-07-18 | 超威电源有限公司 | Method for internalizing valve-regulated lead acid storage battery |
CN103199243A (en) * | 2013-03-14 | 2013-07-10 | 超威电源有限公司 | Positive lead paste of lead-acid storage battery |
-
2013
- 2013-07-15 CN CN201310294296.8A patent/CN104300179A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101901935A (en) * | 2010-07-02 | 2010-12-01 | 超威电源有限公司 | Internal formation process for high-capacity gel battery |
CN102593533A (en) * | 2012-03-15 | 2012-07-18 | 超威电源有限公司 | Method for internalizing valve-regulated lead acid storage battery |
CN103199243A (en) * | 2013-03-14 | 2013-07-10 | 超威电源有限公司 | Positive lead paste of lead-acid storage battery |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107492682A (en) * | 2016-06-13 | 2017-12-19 | 深圳市雄韬电源科技股份有限公司 | Lead-acid accumulator is without recirculated cooling water internal formation process |
CN107681204A (en) * | 2017-09-01 | 2018-02-09 | 超威电源有限公司 | The chemical synthesis technology of the battery prepared using recovery lead powder |
CN109148815A (en) * | 2018-07-18 | 2019-01-04 | 天能电池集团有限公司 | A kind of long-life lead storage battery acid adding chemical synthesizing method |
CN109148815B (en) * | 2018-07-18 | 2021-12-28 | 天能电池集团股份有限公司 | Acidification formation method for long-life lead storage battery |
CN110504495A (en) * | 2019-08-12 | 2019-11-26 | 天能电池集团股份有限公司 | A kind of acid adding chemical synthesizing method of battery |
CN111600085A (en) * | 2020-01-19 | 2020-08-28 | 超威电源集团有限公司 | Method for manufacturing lead-acid storage battery |
CN111416164A (en) * | 2020-03-05 | 2020-07-14 | 天能电池集团股份有限公司 | Storage battery container formation and matching method |
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Application publication date: 20150121 |