CN103560274A - Battery evacuating formation method - Google Patents
Battery evacuating formation method Download PDFInfo
- Publication number
- CN103560274A CN103560274A CN201310527952.4A CN201310527952A CN103560274A CN 103560274 A CN103560274 A CN 103560274A CN 201310527952 A CN201310527952 A CN 201310527952A CN 103560274 A CN103560274 A CN 103560274A
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- China
- Prior art keywords
- battery
- negative pressure
- charging
- electric current
- charges
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Links
- 238000000034 method Methods 0.000 title claims abstract description 26
- 230000015572 biosynthetic process Effects 0.000 title abstract description 9
- 238000007600 charging Methods 0.000 claims abstract description 29
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims abstract description 28
- 239000000126 substance Substances 0.000 claims description 7
- 230000002194 synthesizing effect Effects 0.000 claims description 7
- 238000006243 chemical reaction Methods 0.000 abstract description 8
- 239000002253 acid Substances 0.000 abstract description 7
- 238000004519 manufacturing process Methods 0.000 abstract description 2
- 239000011149 active material Substances 0.000 abstract 2
- 230000003247 decreasing effect Effects 0.000 abstract 1
- 229910000464 lead oxide Inorganic materials 0.000 description 9
- YEXPOXQUZXUXJW-UHFFFAOYSA-N oxolead Chemical group [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 description 9
- PIJPYDMVFNTHIP-UHFFFAOYSA-L lead sulfate Chemical compound [PbH4+2].[O-]S([O-])(=O)=O PIJPYDMVFNTHIP-UHFFFAOYSA-L 0.000 description 4
- 206010011906 Death Diseases 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 230000008595 infiltration Effects 0.000 description 2
- 238000001764 infiltration Methods 0.000 description 2
- WABPQHHGFIMREM-UHFFFAOYSA-N lead(0) Chemical compound [Pb] WABPQHHGFIMREM-UHFFFAOYSA-N 0.000 description 2
- 230000000740 bleeding effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Images
Classifications
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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
-
- 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
- H01M10/42—Methods or arrangements for servicing or maintenance of secondary cells or secondary half-cells
- H01M10/4242—Regeneration of electrolyte or reactants
-
- 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
- H01M10/42—Methods or arrangements for servicing or maintenance of secondary cells or secondary half-cells
- H01M10/44—Methods for charging or discharging
-
- 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)
- Secondary Cells (AREA)
- Battery Electrode And Active Subsutance (AREA)
Abstract
The invention relates to a battery manufacturing method, and in particular relates to a battery evacuating formation method. When a charger (1) charges a battery (3) through a wire (2), a great amount of gas is generated inside the battery to raise sulfuric acid in the battery into an acid pot (4) above the battery, a negative pressure generator (6) generates negative pressure, the acid pot is sucked to negative pressure through a gas pipe (5), and gas in the battery (3) is timely discharged; meanwhile, the sulfuric acid in the acid pot is timely filled into the battery for reaction; during formation of the battery, the battery is evacuated to enable the sulfuric acid to completely penetrate into a lead active material, so that the conversion uniformity of the active material is improved, the formation efficiency is improved, the charging amount is decreased, and the charging time is shortened.
Description
Technical field
The present invention relates to a kind of manufacture processing method of battery, more specifically, relate to a kind of battery vacuum formation method.
Background technology
The principle of electric weight is changed and stored to lead acid accumulator being: lead powder is lead oxide, generate lead sulfate with sulfuric acid infiltration, at positive pole after overcharging, convert brown lead oxide to, negative machine converts porous lead to, the velvet-like porous lead of so anodal brown lead oxide, negative pole, together with sulfuric acid, just forms the battery that can store electric weight.This transfer process is also common " life thing is changed the process of ripe being ".
Shortcoming: because battery can generate heat when charging, produce a large amount of bubbles, this bubble is by the sulfuric acid jack-up of inside battery, acid and plumbous being permeable reactive are insufficient like this, while causing charging, lead powder is much still the state existence of lead oxide, so just hinder the formation efficiency of lead sulfate, also hindered the formation efficiency of brown lead oxide simultaneously.Cause needing a large amount of chargings, need charge for a long time, waste electric weight, has reduced formation efficiency.
Summary of the invention
Technical problem to be solved by this invention is, when battery changes into, battery carried out to exhaust, be beneficial to sulfuric acid completely with plumbous being infiltration, thereby put forward being conversion uniformity, improve formation efficiency, reduce charge volume and charging interval.
The chemical synthesizing method of finding time, described method comprises:
3 stages: the first stage: electric current charges to battery, charge and vacuumize negative pressure Exhaust Gas for 1~3 hour; Second stage: electric current charges to battery, charges and within 23~29 hours, vacuumizes negative pressure Exhaust Gas, and three phases: electric current charges to battery charges and within 9~11 hours, vacuumizes negative pressure Exhaust Gas;
3 stages are the method for charging and vacuumizing, method is: when charger process wire is when charging for battery, inside battery produces a large amount of gas, the sulfuric acid jack-up in battery, top is in the sour kettle of battery top, and negative pressure generator produces negative pressure, by tracheae, on sour kettle, takes out negative pressure, gas in battery is discharged in time, and the sulfuric acid in sour kettle of while is filled in time inside battery and reacts;
Described negative pressure is-0.06~0.085MPa.
The described first stage, the electric current of battery charging is 0.12~0.13 times of battery capacity; Second stage, the electric current of battery charging is 0.205~0.215 times of battery capacity; Phase III, the electric current of battery charging is 0.12~0.13 times of battery capacity.
Beneficial effect:
In charging process, adopt the foam method method of bleeding, by negative pressure, the gas of inside battery is extracted out, sulfuric acid is fully permeated in plumbous being, so just aggravate the speed of lead oxide generation lead sulfate, also further aggravate lead sulfate and convert brown lead oxide speed to, thereby reduce charge volume 20%, reduce the charging interval 20%, the battery being conversion uniformity of air-discharging charging improves, and deviation is generally less than 4%, and battery life improves 30%.The active conversion uniformity improves in Table 1, and battery life situation is in Table 2.
Table 1: the being conversion uniformity improves
Pole plate position | Normal charge changes into being conversion brown lead oxide ratio (%) | Utilize the battery of the present invention chemical synthesizing method being conversion brown lead oxide ratio (%) of finding time |
Top | 93 | 91 |
Middle part | 88 | 89 |
Bottom | 83 | 87 |
Extreme difference | 10 | 4 |
Table 2: battery life situation
Cycle-index (inferior) | Discharge time (minute) | Discharge time (minute) |
50 | 125 | 125 |
100 | 120 | 122 |
150 | 112 | 115 |
200 | 102 | 110 |
250 | 95 | 105 |
300 | 84(end-of-life) | 99 |
350 | ? | 94 |
390 | ? | 84(end-of-life) |
General vacuum is 0Mpa, and herein indication to vacuumize actual be to be pumped into negative pressure state, also lower than vacuum, for-0.06~-0.085MPa, and conventional atmospheric pressure is 133.32pa, so be that wearing or featuring stage armour inside battery is pumped into negative pressure state bubble is extracted out, then by atmospheric pressure, acid fracturing being entered in pole plate is battery bottom, its plumbous and acid fully contact and react thorough afterwards.
Accompanying drawing explanation:
Fig. 1 is appearance structure schematic diagram of the present invention
In Fig. 1,1 is charger, and 2 is wire, and 3 is battery, and 4 is sour kettle, and 5 is tracheae, and 6 is negative pressure generator
Embodiment:
The chemical synthesizing method of finding time,
3 stages: first stage: electric current, to battery (3) charging, charges and vacuumizes negative pressure Exhaust Gas for 1~3 hour; Second stage: electric current charges to battery, charges and within 23~29 hours, vacuumizes negative pressure Exhaust Gas, and three phases: electric current charges to battery charges and within 9~11 hours, vacuumizes negative pressure Exhaust Gas;
3 stages are the method for charging and vacuumizing, method is: when charger (1) process wire (2) is when for battery (3) charging, inside battery produces a large amount of gas, the sulfuric acid jack-up in battery, top is in the sour kettle (4) of battery top, and negative pressure generator (6) produces negative pressure, by tracheae (5), on sour kettle (4), takes out negative pressure, gas in battery (3) is discharged in time, and the sulfuric acid in sour kettle of while is filled in time inside battery and reacts;
Described negative pressure is-0.06~0.085MPa.
The described first stage, the electric current of battery charging is 0.12~0.13 times of battery capacity numerical value; Second stage, the electric current of battery charging is 0.205~0.215 times of battery capacity numerical value; Phase III, the electric current of battery charging is 0.12~0.13 times of battery capacity numerical value; For example, when battery capacity is 12Ah, the charging current of first stage is 1.44~1.56A; Second stage, the electric current of battery charging is 2.46~2.58A; Phase III, charging current is 1.44~1.56A.
Claims (3)
1. the battery chemical synthesizing method of finding time, is characterized in that, described method comprises:
3 stages: first stage: electric current, to battery (3) charging, charges and vacuumizes negative pressure Exhaust Gas for 1~3 hour; Second stage: electric current charges to battery, charges and within 23~29 hours, vacuumizes negative pressure Exhaust Gas, and three phases: electric current charges to battery charges and within 9~11 hours, vacuumizes negative pressure Exhaust Gas;
3 stages are the method for charging and vacuumizing, method is: when charger (1) process wire (2) is when for battery (3) charging, inside battery produces a large amount of gas, the sulfuric acid jack-up in battery, top is in the sour kettle (4) of battery top, and negative pressure generator (6) produces negative pressure, by tracheae (5), on sour kettle (4), takes out negative pressure, gas in battery (3) is discharged in time, and the sulfuric acid in sour kettle of while is filled in time inside battery and reacts.
2. the battery according to claim 1 chemical synthesizing method of finding time, is characterized in that, described negative pressure is-0.06~0.085MPa.
3. the battery according to claim 1 chemical synthesizing method of finding time, is characterized in that, the described first stage, the electric current of battery charging is 0.12~0.13 times of battery capacity; Second stage, the electric current of battery charging is 0.205~0.215 times of battery capacity; Phase III, the electric current of battery charging is 0.12~0.13 times of battery capacity.
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CN201310527952.4A CN103560274B (en) | 2013-10-31 | 2013-10-31 | Battery evacuates chemical synthesizing method |
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CN201310527952.4A CN103560274B (en) | 2013-10-31 | 2013-10-31 | Battery evacuates chemical synthesizing method |
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CN103560274A true CN103560274A (en) | 2014-02-05 |
CN103560274B CN103560274B (en) | 2016-08-24 |
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104614678A (en) * | 2015-01-21 | 2015-05-13 | 哈尔滨工业大学 | Online detection device and method of battery electrode level in lead-acid storage battery inner chemosynthesis process |
CN106299490A (en) * | 2016-08-23 | 2017-01-04 | 超威电源有限公司 | A kind of lead-acid battery formation method |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102315489A (en) * | 2011-08-29 | 2012-01-11 | 风帆股份有限公司 | Method for formation of colloid storage battery of electric vehicle |
CN103296318A (en) * | 2013-05-30 | 2013-09-11 | 江西新威动力能源科技有限公司 | Lead-acid storage battery quantitative closed intermittent container formation device and process |
-
2013
- 2013-10-31 CN CN201310527952.4A patent/CN103560274B/en active Active
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102315489A (en) * | 2011-08-29 | 2012-01-11 | 风帆股份有限公司 | Method for formation of colloid storage battery of electric vehicle |
CN103296318A (en) * | 2013-05-30 | 2013-09-11 | 江西新威动力能源科技有限公司 | Lead-acid storage battery quantitative closed intermittent container formation device and process |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104614678A (en) * | 2015-01-21 | 2015-05-13 | 哈尔滨工业大学 | Online detection device and method of battery electrode level in lead-acid storage battery inner chemosynthesis process |
CN104614678B (en) * | 2015-01-21 | 2017-08-25 | 哈尔滨工业大学 | A kind of lead-acid accumulator is internalized into the on-line measuring device and method of process battery electrode current potential |
CN106299490A (en) * | 2016-08-23 | 2017-01-04 | 超威电源有限公司 | A kind of lead-acid battery formation method |
CN106299490B (en) * | 2016-08-23 | 2019-03-12 | 超威电源有限公司 | A kind of lead-acid battery formation method |
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Address after: 454550 Qinnan Industrial Zone, Qinyang City, Jiaozuo City, Henan Province Patentee after: Henan Biaoxin Power Supply Co.,Ltd. Country or region after: China Address before: 454550 Qinnan Industrial Zone, Qinyang City, Jiaozuo City, Henan Province Patentee before: HENAN CHAOWEI POWER SUPPLY Co.,Ltd. Country or region before: China |