CN104485445A - Positive plate used for lead-acid storage battery and preparation method of positive plate - Google Patents
Positive plate used for lead-acid storage battery and preparation method of positive plate Download PDFInfo
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- CN104485445A CN104485445A CN201410828026.5A CN201410828026A CN104485445A CN 104485445 A CN104485445 A CN 104485445A CN 201410828026 A CN201410828026 A CN 201410828026A CN 104485445 A CN104485445 A CN 104485445A
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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
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/14—Electrodes for lead-acid accumulators
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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
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/14—Electrodes for lead-acid accumulators
- H01M4/16—Processes of manufacture
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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
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/14—Electrodes for lead-acid accumulators
- H01M4/16—Processes of manufacture
- H01M4/20—Processes of manufacture of pasted electrodes
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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
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/14—Electrodes for lead-acid accumulators
- H01M4/16—Processes of manufacture
- H01M4/20—Processes of manufacture of pasted electrodes
- H01M4/21—Drying of pasted electrodes
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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
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/64—Carriers or collectors
- H01M4/66—Selection of materials
- H01M4/68—Selection of materials for use in lead-acid accumulators
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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
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/64—Carriers or collectors
- H01M4/70—Carriers or collectors characterised by shape or form
- H01M4/72—Grids
- H01M4/73—Grids for lead-acid accumulators, e.g. frame plates
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- 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
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Abstract
The inventionprovides a positive plate used for a lead-acid storage battery. The positive plate comprises an alloy plate grid and lead-acid layers coating two surfaces of the alloy plate grid, wherein the alloy plate grid is prepared from the following components in percentage by weight: 0.05-0.2% of calcium, 0.6-1.0% of tin, 0.01-0.05% of aluminum and the balance of lead;each lead-acid layer is mainly prepared from the following components in parts by weight: 950-1050 parts of lead powder, 100-110 parts of water and 90-100 parts of sulfuric acid in the specification of 1.4g/cm3. The lead-acid storage battery with the positive platehas the advantages of good heavy-current discharge stability, highlow-temperature start capacity, excellentanti-corrosion performance, longcirculating charge and discharge life and excellent comprehensive performance.
Description
Technical field
The present invention relates to Lead-acid Battery Technology field, be specifically related to a kind of positive plate for lead acid accumulator, and this is used for the preparation method of the positive plate of lead acid accumulator.
Background technology
Lead acid accumulator (VRLA), be that a kind of electrode is made primarily of plumbous and oxide, electrolyte is the storage battery of sulfuric acid solution.Under lead-acid battery state-of-charge, positive pole main component is brown lead oxide, and negative pole main component is plumbous; Under discharge condition, the main component of both positive and negative polarity is lead sulfate.
For lead acid accumulator, battery lead plate is one of vital parts, and the quality of its quality is directly connected to quality and the useful life of whole lead acid accumulator.Battery lead plate mainly contains alloy grid and is coated in the active coating formation of alloy grid, and wherein alloy grid is mainly Pb-Ca-Sn alloy, and active coating is mainly the coating containing Sn and Pb.Although this battery lead plate possesses good stable charge/discharge, overall synthetic performance is not good, such as than can low, useful life is short and regular maintenance is frequent.
Summary of the invention
Technical problem to be solved by this invention is the deficiency for above prior art problem, a kind of positive plate for lead acid accumulator is provided, use the good stability of the lead acid accumulator heavy-current discharge of this positive plate, Low temperature start-ability is strong, excellent anti-corrosion performance, cycle charge discharge electric life is long, high comprehensive performance.
The technical solution adopted in the present invention is:
A kind of positive plate for lead acid accumulator, this positive plate comprises alloy grid and is overlying on the plumbic acid layer on alloy grid two sides, described alloy grid is prepared from by each component of following percentage by weight: calcium 0.05-0.2%, tin 0.6-1.0%, aluminium 0.01-0.05%, remaining as lead, described plumbic acid layer is prepared from primarily of each component of following parts by weight: lead powder 950-1050 part, water 100-110 part, 1.4g/cm
3sulfuric acid 90-100 part.
As preferably, described alloy grid is prepared from by each component of following percentage by weight: calcium 0.1%, tin 0.8%, aluminium 0.03%, remaining as lead.
As preferably, described plumbic acid layer is prepared from primarily of each component of following parts by weight: 1000 ± 1.0 parts, lead powder, 105 ± 0.5 parts, water, 1.4g/cm
396.00 ± 0.2 parts, sulfuric acid.
As preferably, the thickness of described alloy grid is 1.0-4.4mm, and the thickness of described plumbic acid layer is 0.15mm.
The present invention further provides the preparation method of the above-mentioned positive plate for lead acid accumulator, specifically comprise the following steps:
(1) alloy grid casting:
Carry out at automatic grid slab machine, lead pig is dropped into the market pot of automatic grid slab machine, being warming up to 430-470 DEG C (being preferably 450 DEG C) makes lead pig melt, keep plumbous liquid liquid look to be silvery white, described lead pig comprises each component of following percentage by weight: calcium 0.05-0.2%, tin 0.6-1.0%, aluminium 0.01-0.05%, remaining as lead; The plumbous liquid formed after fusing enters mould cast molding through cannelure, lead pipe, and the temperature of described mould is 170-190 DEG C (being preferably 180 DEG C), poring rate be 12-17 sheet/minute, obtain alloy grid, for subsequent use.
Be sprayed with jet mould agent in described mould, the preparation method of described jet mould agent is as follows: add 4g gelatine, 1g polyethylene fibre in every 1000g water, add 150g wood powder again and stir, be jet mould agent after cooling after boiling.
In this step, lead pig fusion temperature is extremely important, must not be too high or too low, time too low, and plumbous fluid valve and put plumbous mouth and easily block up, plumbous liquid not easily flows into cannelure, causes to fill type and be discontented with; Time too high, the scaling loss of plumbous liquid is serious, easily pollutes and wastes, also can cause disconnected bar slowly because leads is cooled.
The quality of the agent of cast link jet mould, poring rate, mold temperature alloy grid is also most important, and in jet mould agent, wood powder is too many, and casting rate is too fast, and the alloy grid of casting is easy to crack, and in jet mould agent, wood powder very little, and Mo Wentai is low, and alloy grid forming quality is poor.
(2) lead powder preparation: cylinder lead being dropped into lead-power machine carries out abrasive dust, and arranging temperature in lead-power machine cylinder is 130-140 DEG C, and load power is 90kW, air door positive wine pressure is 2000pa ± 150pa, blast born by air door is 3600 ± 150pa, and powder delivery speed is 0.8 ton/hour, obtains lead powder.
The process parameter control that lead powder manufactures is extremely important, and lead-power machine load capacity (being reflected by load power), air quantity, temperature etc. all can affect lead powder Quality and yield.
Cylinder planted agent avoids producing high temperature, and air quantity is too small, and in cylinder, temperature is too high, and material continues oxidation intensification together because heaping, and degree of oxidation of lead powder can be made high, and viscosity increases, and forms very dangerous burn-off phenomenon, and bearing shell and carrying roller performance depreciation, cause wearing and tearing; Adjustment negative-pressure air fan is the important step determining lead powder output, and when load is certain, suitably improving negative pressure wind is to make output increase, but lead powder granularity is also thereupon amid a sharp increase, and oxidizability reduces, so the adjustment of negative-pressure air fan should with lead powder quality for foundation.
Apparent density and oxidizability detect two large important indicators of lead powder quality, and load is excessive, lead button is too much, and barrel temperature is low, positive and negative blast is excessive, air quantity too big city make apparent density of lead powder higher, oxidizability is on the low side, and vice versa.When improving apparent density of lead powder, oxidizability can decline, and brush excess, sheet lead increase than regular meeting, so suitably should adjust temperature; The oxidizability temperature influence of lead powder is comparatively large, simultaneously also by the impact of blast, ambient temperature and humidity.
After the above state modulator of the present invention, the apparent density of lead powder obtained reaches 1.25-1.35g/cm
3, oxidizability is 72-78%.
Measurement of apparent density method: allow lead powder by 80 order sub-sieves, freely falling body is in the steel bowl of 100ml, and fall completely and strike off gently, weigh as G gram, steel bowl is heavily G
0gram, then apparent density d=(G-G
0)/100 (g/cm
3).
(3) lead plaster preparation: after taking the lead powder of formulation weight, water and sulfuric acid, drop into successively and close cream machine, arranging and closing cream temperature is 44-46 DEG C, the dry conjunction time (mixing time to before lead powder to feedwater) is 3-5min, the wet conjunction time (feedwater to the mixing time before sulfuric acid) for 6-10min, incorporation time (mixing time to after sulfuric acid) be 20-25min.
When mixing in this step, (sulfuric acid adds fashionable) control temperature is at 55-65 DEG C.
(4) coated plate: use coating machine by the two sides of lead plaster roll coated in alloy grid, then through drenching pure water, drench acid, dry tack free, cream more than cleaning, obtain green plate.
The pouring acid solution of drenching acid use in this step is sulfuric acid solution, and density is 1.08-1.09g/cm
3(25 DEG C).
(5) green plate solidification, dry: green plate temperature 40-50 DEG C, be cured drying under the environmental condition of relative humidity >=97%, arranging solidification flow process is: 50 DEG C of 24h, 52 DEG C of 4h, 50 DEG C of 8h, 50 DEG C of 8h, 52 DEG C of 6h, 55 DEG C of 6h, 60 DEG C of 2h, 65 DEG C of 2h, 70 DEG C of 2h, 80 DEG C of 8h.
The design of the environmental condition that this step is solidified and solidification flow process is extremely important, solidification is dry adopts special steam heating, make green plate not easy to crack in the process of solidification, the pole plate obtained after using above solidification drying is through test, free lead content≤3%, water content≤0.5%, this effectively prevent the generation of the situations such as active material layer poor response, coating absent-mindedness, poor performance, is very beneficial for finished electrode plate dark charge and discharge cycle performance in use and resistance to overturning.
(6) welding changes into: be placed in electrolytic bath by dried for solidification pole plate and carry out changing into process, in electrolytic bath, sulfuric acid solution density is 1.04-1.06g/cm
3(25 DEG C), in groove, electric current is 100-130A, and the time of changing into is 18-19h, makes pole plate charged.
(7) dry: finally in oxygen-free drier, carry out drying, at first stage 45-50 DEG C temperature, 26-38h at 10h, second stage 73-83 DEG C temperature, obtains the positive plate for lead acid accumulator.
Compared with prior art, the present invention possesses following advantage and remarkable result: positive plate of the present invention is for the good stability of heavy-current discharge after lead acid accumulator, Low temperature start-ability is strong, excellent anti-corrosion performance, cycle charge discharge electric life is long, high comprehensive performance, and this depends on the present invention to the optimization of formula and the accurate control to manufacture craft links, and recipe optimization, synergy good between each process procedure, be embodied in:
(1) on the formula of grid, choosing by particular components, particularly selecting of al composition effectively avoids Calcium compounds scaling loss in sintering procedure, and optimizes the proportioning of each component, makes the grid size specification obtained, not easy to crack, mechanical strength is high, corrosion resistance and good, conducts electricity very well, higher than energy, capacitance is stablized;
(2) in the formulation selection of active material layer, choose the lead powder of apparent density and oxidizability excellence, again by optimizing the formula of lead plaster, optimize the design proportion of grid and active material, make grid and active material have good adhesion, the battery lead plate free lead content obtained is few, be conducive to dark charge and discharge circulation and the discharge stability of storage battery, charge storage ability is strong, long service life, and Low temperature start-ability is strong;
(3) in preparation method, by strictly controlling and the technological parameter of the links such as the casting of optimized alloy grid, lead powder preparation, lead plaster preparation, coated plate, green plate solidifies, welding changes into, drying, thus the strict quality controlling each intermediate product, and make to coordinate well between links, thus make the battery lead plate power reservoir capacity that obtains strong, self discharge is little, heavy-current discharge good stability, Low temperature start-ability is strong, excellent anti-corrosion performance, cycle charge discharge electric life is long, high comprehensive performance, total preparation cost is low, is suitable for and promotes.
Embodiment
Below in conjunction with embodiment, the present invention is further described in detail.Iting is noted that following illustrating is all exemplary, being intended to the invention provides further instruction.Except as otherwise noted, all Science and Technology terms that the present invention uses have the identical meanings usually understood with the technical field of the invention personnel.
1, material
(alloy) lead pig is purchased from Zhuzhou Smelter Group Co., Ltd.; Lead purity 99.994%.
2, process equipment:
Automatic grid slab machine innovates Machinery Co., Ltd. purchased from Quanzhou City Feng Ze; SF-2OLS type winnowing type lead-power machine is purchased from Central-South Industrial Co., Ltd.; MAM-680 screw air compressor is purchased from mountain and sea Yu Neng Co., Ltd of Shenzhen; Full-automatic conjunction cream machine (specification 1000kg) is purchased from Central-South Industrial Co., Ltd.; YG-STB400 dual-side coating machine is purchased from Baoding Gold Sunshine Energy Equipment Technology Co., Ltd.; Full-automatic solidification drying system is purchased from Central-South Industrial Co., Ltd..
Embodiment 1:
The positive plate that the present embodiment is used for lead acid accumulator comprises alloy grid and is overlying on the plumbic acid layer on alloy grid two sides, and the thickness of described alloy grid is 2.4mm, and the thickness of described plumbic acid layer is 0.15mm.Described alloy grid is prepared from by each component of following percentage by weight: calcium 0.1%, tin 0.8%, aluminium 0.03%, remaining as lead.Described plumbic acid layer is prepared from primarily of each component of following parts by weight: 1000 ± 1.0 parts, lead powder, 105 ± 0.5 parts, water, 1.4g/cm
396.00 ± 0.2 parts, sulfuric acid.
The preparation method of above-mentioned positive plate, specifically comprises the following steps:
(1) alloy grid casting: carry out at automatic grid slab machine, lead pig is dropped into the market pot of automatic grid slab machine, being warming up to 450 DEG C makes lead pig melt, keep plumbous liquid liquid look to be silvery white, described lead pig comprises each component of following percentage by weight: calcium 0.1%, tin 0.8%, aluminium 0.03%, remaining as lead; Through cannelure, (cannelure temperature is controlled by cooling water the plumbous liquid formed after fusing, by regulating cooling water flow, make plumbous in cannelure, to keep the long liquid zone of 250-300mm), lead pipe enters mould cast molding, jet mould agent (jet mould agent preparation method: add 4g gelatine, 1g polyethylene fibre in every 1000g water is sprayed with in mould, add 150g wood powder after boiling again to stir, be jet mould agent after cooling), the temperature of described mould is 180 DEG C, poring rate is 15 slices/minute, obtain alloy grid, for subsequent use;
(2) lead powder preparation: cylinder lead being dropped into lead-power machine carries out abrasive dust, arranging temperature in lead-power machine cylinder is 135 DEG C, in cylinder, the weight of lead is no more than 2000kg (being generally about 1.8 tons), load power is 90kW, air door positive wine pressure is 2000pa, blast born by air door is 3600pa, and powder delivery speed is 0.8 ton/hour, obtains lead powder;
(3) lead plaster preparation: take the lead powder of formulation weight, water and sulfuric acid, after conjunction cream machine starts normal operation, arranging and closing cream temperature is 45 DEG C, add lead powder successively, dry stirring 3min, adds pure water, wet stirring 8min, acid adding (control temperature is at 55-65 DEG C), finally stirs 23min, forms lead plaster;
(4) coated plate: use coating machine by the two sides of lead plaster roll coated in alloy grid, then through drench pure water, drench acid (pouring acid solution is sulfuric acid solution, density 1.08 ~ 1.09g/cm
3, 25 DEG C), dry tack free (this step dewater about 9-10%), the remaining cream of cleaning, obtain green plate;
(5) green plate solidification, dry: green plate temperature 40-50 DEG C, be cured drying under the environmental condition of relative humidity >=97%, arranging solidification flow process is: 50 DEG C 24 hours, 52 DEG C 4 hours, 50 DEG C 8 hours, 50 DEG C 8 hours, 52 DEG C 6 hours, 55 DEG C 6 hours, 60 DEG C 2 hours, 65 DEG C 2 hours, 70 DEG C 2 hours, 80 DEG C 8 hours;
(6) welding changes into: be placed in electrolytic bath by dried for solidification pole plate and carry out changing into process, in electrolytic bath, sulfuric acid solution density is 1.05g/cm
3(25 DEG C), in groove, electric current is 115A, and the time of changing into is 18.5 hours;
(7) dry: finally in oxygen-free drier, carry out drying, 10h at first stage 48 DEG C of temperature, 32h at second stage 78 DEG C of temperature, obtains the positive plate for lead acid accumulator.
Carry out performance parameter test to the battery lead plate obtained above, result is as shown in table 1 below.
Table 1
| Physical and chemical index | Detect data |
| PbO 2 | 75-85％ |
| Moisture | 0.1-0.5％ |
| Iron (Fe) content | 0.006％ |
| Chlorine (Cl) content | 0.0001％ |
After the battery lead plate using this to obtain makes lead acid accumulator, after testing, carrying capacity can reach 12.8V.
The material that the embodiment of the present invention relates to, reagent and experimental facilities, if no special instructions, be the commercially available prod meeting lead acid accumulator field.
The above, be only the preferred embodiments of the present invention, should be understood that; for those skilled in the art; under the prerequisite not departing from core technology of the present invention, can also make improvements and modifications, these improvements and modifications also should belong to scope of patent protection of the present invention.Any change in the implication suitable with claims of the present invention and scope, all should think to be included in the scope of claims.
Claims (9)
1. the positive plate for lead acid accumulator, it is characterized in that: comprise alloy grid and the plumbic acid layer being overlying on alloy grid two sides, described alloy grid is prepared from by each component of following percentage by weight: calcium 0.05-0.2%, tin 0.6-1.0%, aluminium 0.01-0.05%, remaining as lead, described plumbic acid layer is prepared from primarily of each component of following parts by weight: lead powder 950-1050 part, water 100-110 part, 1.4g/cm
3sulfuric acid 90-100 part.
2. the positive plate for lead acid accumulator according to claim 1, is characterized in that: described alloy grid is prepared from by each component of following percentage by weight: calcium 0.1%, tin 0.8%, aluminium 0.03%, remaining as lead.
3. the positive plate for lead acid accumulator according to claim 1, is characterized in that: described plumbic acid layer is prepared from primarily of each component of following parts by weight: 1000 ± 1.0 parts, lead powder, 105 ± 0.5 parts, water, 1.4g/cm
396.00 ± 0.2 parts, sulfuric acid.
4. the positive plate for lead acid accumulator according to claim 1, is characterized in that: the thickness of described alloy grid is 1.0-4.4mm, and the thickness of described plumbic acid layer is 0.15mm.
5. the preparation method of the positive plate for lead acid accumulator according to claim 1, is characterized in that comprising the following steps:
(1) alloy grid casting: market pot lead pig being dropped into grid slab machine, being warming up to 430-470 DEG C makes lead pig melt, and described lead pig comprises each component of following percentage by weight: calcium 0.05-0.2%, tin 0.6-1.0%, aluminium 0.01-0.05%, remaining as lead; The plumbous liquid formed after fusing enters mould cast molding through cannelure, lead pipe, and the temperature of described mould is 170-190 DEG C, obtains alloy grid, for subsequent use;
(2) lead powder preparation: cylinder lead being dropped into lead-power machine carries out abrasive dust, and arranging temperature in lead-power machine cylinder is 130-140 DEG C, and load power is 90kW, air door positive wine pressure is 2000 ± 150pa, blast born by air door is 3600 ± 150pa, and powder delivery speed is 0.8 ton/hour, obtains lead powder;
(3) lead plaster preparation: after taking the lead powder of formulation weight, water and sulfuric acid, drops into successively and closes cream machine, and arranging and closing cream temperature is 44-46 DEG C, and the dry conjunction time is 3-5min, the wet conjunction time is 6-10min, incorporation time is 20-25min, forms lead plaster;
(4) coated plate: use coating machine by the two sides of lead plaster roll coated in alloy grid, then through drenching pure water, drench acid, dry tack free, cream more than cleaning, obtain green plate;
(5) green plate solidification, dry: green plate temperature 40-50 DEG C, be cured drying under the environmental condition of relative humidity >=97%, arranging solidification flow process is: 50 DEG C of 24h, 52 DEG C of 4h, 50 DEG C of 16h, 52 DEG C of 6h, 55 DEG C of 6h, 60 DEG C of 2h, 65 DEG C of 2h, 70 DEG C of 2h, 80 DEG C of 8h;
(6) welding changes into: be placed in electrolytic bath by dried for solidification pole plate and carry out changing into process, in electrolytic bath, sulfuric acid solution density is 1.04-1.06g/cm
3, in groove, electric current is 100-130A, and the time of changing into is 18-19h;
(7) dry: finally in oxygen-free drier, carry out drying, at first stage 45-50 DEG C temperature, 26-38h at 10h, second stage 73-83 DEG C temperature, obtains the positive plate for lead acid accumulator.
6. the preparation method of the positive plate for lead acid accumulator according to claim 5, is characterized in that: the temperature that in described step (1), lead pig melts is 450 DEG C, and the temperature of mould is 180 DEG C.
7. the preparation method of the positive plate for lead acid accumulator according to claim 5, it is characterized in that: in described step (1), in mould, be sprayed with jet mould agent, the preparation method of described jet mould agent is as follows: add 4g gelatine, 1g polyethylene fibre in every 1000g water, add 150g wood powder after boiling again to stir, be jet mould agent after cooling.
8. the preparation method of the positive plate for lead acid accumulator according to claim 5, is characterized in that: when mixing in described step (3), control temperature is at 55-65 DEG C.
9. the preparation method of the positive plate for lead acid accumulator according to claim 5, is characterized in that: the pouring acid solution of drenching acid use in described step (4) is sulfuric acid solution, and density is 1.08-1.09g/cm
3.
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Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
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| CN105098278A (en) * | 2015-08-03 | 2015-11-25 | 安徽新能电源科技有限公司 | Reuse technology for waste rare-earth alloy hanging bar lead |
| CN106169562A (en) * | 2016-08-03 | 2016-11-30 | 湖北润阳新能源有限公司 | Solidifying lead acid battery polar plate frame and preparation technology thereof |
| CN109119596A (en) * | 2018-08-01 | 2019-01-01 | 天能电池(芜湖)有限公司 | A kind of ultrathin plate manufacturing method |
| CN111710836A (en) * | 2020-06-24 | 2020-09-25 | 山东修车匠车业有限公司 | Curing process for positive plate of lead-acid storage battery for electric automobile |
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| CN1967912A (en) * | 2005-11-18 | 2007-05-23 | 上海耀国能源科技有限公司 | Polar plate and electrolyte of lead storage battery applied for electromotion aid car |
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Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
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| CN105098278A (en) * | 2015-08-03 | 2015-11-25 | 安徽新能电源科技有限公司 | Reuse technology for waste rare-earth alloy hanging bar lead |
| CN106169562A (en) * | 2016-08-03 | 2016-11-30 | 湖北润阳新能源有限公司 | Solidifying lead acid battery polar plate frame and preparation technology thereof |
| CN109119596A (en) * | 2018-08-01 | 2019-01-01 | 天能电池(芜湖)有限公司 | A kind of ultrathin plate manufacturing method |
| CN111710836A (en) * | 2020-06-24 | 2020-09-25 | 山东修车匠车业有限公司 | Curing process for positive plate of lead-acid storage battery for electric automobile |
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| CN104485445B (en) | 2017-02-22 |
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