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JP2982368B2 - Battery storage method for lead-acid batteries - Google Patents

Battery storage method for lead-acid batteries

Info

Publication number
JP2982368B2
JP2982368B2 JP3111604A JP11160491A JP2982368B2 JP 2982368 B2 JP2982368 B2 JP 2982368B2 JP 3111604 A JP3111604 A JP 3111604A JP 11160491 A JP11160491 A JP 11160491A JP 2982368 B2 JP2982368 B2 JP 2982368B2
Authority
JP
Japan
Prior art keywords
battery
specific gravity
sulfuric acid
electrolytic solution
stirring
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.)
Expired - Fee Related
Application number
JP3111604A
Other languages
Japanese (ja)
Other versions
JPH04341759A (en
Inventor
和吉 米津
勝弘 高橋
芳雄 仲田
伊佐美 永田
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.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial 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.)
Filing date
Publication date
Application filed by Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP3111604A priority Critical patent/JP2982368B2/en
Publication of JPH04341759A publication Critical patent/JPH04341759A/en
Application granted granted Critical
Publication of JP2982368B2 publication Critical patent/JP2982368B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • 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

Landscapes

  • Filling, Topping-Up Batteries (AREA)
  • Battery Electrode And Active Subsutance (AREA)

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は、鉛蓄電池の電槽化成方
法に関するものであり、特に電槽化成前に低比重の希硫
酸を電槽に注入して用いる方法に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for forming a lead storage battery in a battery case, and more particularly to a method for injecting dilute sulfuric acid having a low specific gravity into a battery case before forming the battery case.

【0002】[0002]

【従来の技術】鉛蓄電池の電槽化成方法には、電槽化成
前に比重1.200程度の希硫酸を注液し、化成中の電
気分解による電解液の濃縮や極板中より生成する硫酸量
を考慮して、その注液量を定め電槽化成を行い、電槽化
成終了後の電解液比重が所定の比重となるようにする方
法がある。また電槽化成の電気量を合理化するために、
1.180以下の低比重の希硫酸を電槽化成前に注液
し、電槽化成終了後にこの化成電解液脱液し、その後
1.400程度の高比重の硫酸を加え、50〜80Aの
大電流にて連続再充電し、短時間の内に電池内部の電解
液を攪拌して、所定の電解液比重に調整する方法もあ
る。なお、現在は後者の方法が主流として多く用いられ
ている。
2. Description of the Related Art In a method for forming a lead-acid battery in a battery case, dilute sulfuric acid having a specific gravity of about 1.200 is injected before the battery case is formed, and the electrolytic solution is concentrated by electrolysis during the formation and is formed from the electrode plate. There is a method in which the amount of the injected solution is determined in consideration of the amount of sulfuric acid and the battery case is formed, so that the specific gravity of the electrolytic solution after the formation of the battery case becomes a predetermined specific gravity. Also, in order to rationalize the amount of electricity for battery formation,
Dilute sulfuric acid having a low specific gravity of 1.180 or less is injected before the formation of the battery case, and after the formation of the battery case, the chemical electrolyte is removed. Then, sulfuric acid having a high specific gravity of about 1.400 is added, and 50 to 80 A of sulfuric acid is added. There is also a method of continuously recharging with a large current and stirring the electrolyte inside the battery within a short time to adjust the specific gravity of the electrolyte to a predetermined value. At the present time, the latter method is mainly used.

【0003】[0003]

【発明が解決しようとする課題】電槽化成の際の電気量
を合理化するために、上記の電槽化成前に注液する希硫
酸の比重を低比重とし、電槽化成終了後脱液して高比重
の硫酸を加え、大電流による連続再充電によって攪拌す
る方法は有効である。しかし攪拌を大電流による連続再
充電する方法頼るため、その時のガス発生が非常に激
しくなる。そのため電槽化成後脱液した後加える高比重
の硫酸が電池上部に浮いてしまい、電池内部に残存する
低比重の電解液と充分に攪拌がなされないことになる。
In order to rationalize the amount of electricity during battery case formation, the specific gravity of the diluted sulfuric acid to be injected before the above-mentioned battery case formation is made low, and after completion of the battery case formation, the liquid is removed. It is effective to add high specific gravity sulfuric acid and stir by continuous recharging with a large current. However, since rely Stirring method for continuously recharged by a large current, the gas generation at that time is very intense. For this reason, sulfuric acid having a high specific gravity, which is added after dewatering after formation of the battery case, floats on the upper part of the battery, and the low specific gravity electrolytic solution remaining inside the battery is not sufficiently stirred.

【0004】従って攪拌後の電解液の比重低下が大き
く、また電解液上部と底部とでの比重差も広がり、濃淡
電池となりやすいなどの大きな課題があった。
[0004] Therefore, there has been a large problem that the specific gravity of the electrolytic solution after the stirring is greatly reduced, and the specific gravity difference between the upper portion and the bottom portion of the electrolytic solution is widened, so that the battery easily becomes a concentration battery.

【0005】[0005]

【課題を解決するための手段】本発明はこのような電槽
化成の合理化を図るため前記の方法を用いた場合の、電
解液の攪拌が充分できないという大きな課題を改善する
ものである。その具体的な手段として、大電流にて再充
電してその際のガス発生により電解液を攪拌して所定の
電解液比重とするとともに、その再充電を通電と通電の
間に2秒以上10秒以下の休止を入れるサイクル充電と
したものである。
SUMMARY OF THE INVENTION The present invention solves a major problem that the stirring of an electrolytic solution cannot be sufficiently performed when the above-described method is used to rationalize the formation of a battery case. As a specific means, while recharging with a large current, agitating the electrolytic solution by gas generation at that time to bring the specific gravity of the electrolytic solution to a predetermined value, the recharging is performed for 2 seconds or more between energizations. This is a cycle charge in which a pause of less than a second is provided.

【0006】[0006]

【作用】つまり従来の大電流にて連続再充電する攪拌方
法においては、再充電にて発生するガスが連続的に電解
液上部に移行するため、脱液後加えた高濃度の硫酸が電
解液上部に舞い上がることになる。そのため脱液後電池
内部に残存する低濃度硫酸と充分な攪拌がなされず、攪
拌後の電解液の比重低下が大きく、また電解液上部と下
部との比重差も拡がり、濃淡電池となり電池寿命が短く
なることがあった。
In other words, in the conventional stirring method of continuously recharging with a large current, since the gas generated by recharging continuously moves to the upper part of the electrolyte, the high-concentration sulfuric acid added after draining removes the electrolyte. Soaring to the top. Therefore, sufficient stirring is not performed with the low-concentration sulfuric acid remaining inside the battery after draining, the specific gravity of the electrolyte after stirring is greatly reduced, and the difference in specific gravity between the upper and lower portions of the electrolyte is also widened, and the battery life becomes a concentration battery and the battery life May be shorter.

【0007】これに対して本発明は、再充電する際に通
電と通電の間に休止を入れることによってガス発生によ
り一旦舞い上がった高濃度の硫酸が、休止期間中に電池
部方向に沈降していくこととなる。そのため低濃度硫
酸と高濃度硫酸が混在する領域が形成され、その状態で
再充電による攪拌が行われるため充分な攪拌がなされる
ことになる。これにより電解液の比重低下が抑制でき、
さらに電解液上部と底部との比重差も解消されるため、
濃淡電池による短寿命という課題も解決することができ
る。
On the other hand, according to the present invention, a high-concentration sulfuric acid once soared due to gas generation by putting a pause between current supply during recharging allows the battery to be charged during the pause.
It will sink down to the bottom . Therefore, a region in which low-concentration sulfuric acid and high-concentration sulfuric acid are mixed is formed, and in this state, stirring is performed by recharging, so that sufficient stirring is performed. Thereby, the specific gravity of the electrolytic solution can be prevented from decreasing,
In addition, the difference in specific gravity between the top and bottom of the electrolyte is also eliminated,
The problem of short life due to the concentration battery can also be solved.

【0008】[0008]

【実施例】以下、本発明の実施例について述べる。Embodiments of the present invention will be described below.

【0009】まず5HR容量で48Ahの電池を作製
し、次いでこの電池(表1)に示す電槽化成条件にて電
槽化成を行った。
First, a battery having a capacity of 5 HR and a capacity of 48 Ah was produced, and then a battery case was formed under the battery forming conditions shown in this battery (Table 1).

【0010】[0010]

【表1】 [Table 1]

【0011】その後電池を反転し脱液した後、攪拌後の
比重が1.280になるように比重1.400の硫酸を
規定量注液した。そして攪拌を行うための再充電電流を
50Aとして1回の通電時間を20秒とし、通電と通電
との間の休止を(表2)に示す各種条件にて総通電時間
が120秒となる再充電攪拌を行った直後の電解液上部
と底部との比重差を図に示す。
After the battery was inverted and drained, a specified amount of sulfuric acid having a specific gravity of 1.400 was injected so that the specific gravity after stirring became 1.280. The re-charging current for stirring is 50 A, and one energizing time is set to 20 seconds, and a pause between energizing times is set to a total energizing time of 120 seconds under various conditions shown in (Table 2). FIG. 1 shows the difference in specific gravity between the top and bottom of the electrolyte immediately after the charging and stirring.

【0012】[0012]

【表2】 [Table 2]

【0013】図1により明らかなように休止時間が0秒
・1秒・11秒のA・B・Eについて電解液上部と底部
との比重差大きく攪拌が充分なされていないことが判
る。これは休止時間がないかまたは1秒と短いA・Bに
ついては、電解液上部に舞い上がった高濃度硫酸が電解
液底部に沈降する時間が維持できない。また休止時間の
長いEについては逆にその時間が長すぎるため高濃度硫
酸が完全に電解液底部に沈降してしまうためによるもの
と推定される。
[0013] It a difference in specific gravity is large stirring more downtime as apparent zero seconds, 1 second, 11 seconds A-B-with electrodeposition Kaieki top and bottom E in FIG. 1 has not been sufficiently I understand. This is because there is no pause time or a short period of 1 second, AB, cannot maintain the time for the high-concentration sulfuric acid soaring at the top of the electrolyte to settle to the bottom of the electrolyte. On the other hand, it is presumed that the high concentration sulfuric acid completely settles at the bottom of the electrolytic solution because E has a long resting time, which is too long.

【0014】これらに対して休止時間が2秒・10秒の
C・Dについては電解液の上部と底部の比重差ほとん
どなく攪拌がほぼ完全になされていることが判る。
[0014] It can be seen that stirring difference in specific gravity without etc. photons <br/> the top and bottom of the electrolytic solution for C-D of downtime for these two seconds, 10 seconds has been almost completely .

【0015】[0015]

【発明の効果】以上のように本発明によれば、従来の電
槽化成前に注液する希硫酸の比重を低比重として、化成
終了後に脱液した後高比重の硫酸を加え大電流にて連続
再充電攪拌をするという電槽化成方法での大きな課題で
あった充分な電解液の攪拌ができないという問題を解決
し、電槽化成の合理化が図れるものである。
As described above, according to the present invention, the specific gravity of the diluted sulfuric acid injected before the conventional battery case formation is set to a low specific gravity, and after the formation, the liquid is removed and high specific gravity sulfuric acid is added to increase the current. This solves the problem of insufficient stirring of the electrolytic solution, which was a major problem in the battery case formation method of continuous recharging and stirring, and rationalizes the case formation.

【図面の簡単な説明】[Brief description of the drawings]

【図1】攪拌再充電時の休止時間別による電解液上部と
底部との比重差を示す図
FIG. 1 is a diagram showing a specific gravity difference between an upper portion and a lower portion of an electrolytic solution according to a rest time during stirring and recharging.

【符号の説明】[Explanation of symbols]

A 休止時間0秒 B 休止時間1秒 C 休止時間2秒 D 休止時間10秒 E 休止時間11秒 A Pause time 0 sec. B Pause time 1 sec. C Pause time 2 sec. D Pause time 10 sec. E Pause time 11 sec.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 永田 伊佐美 大阪府門真市大字門真1006番地 松下電 器産業株式会社内 (56)参考文献 特開 昭57−124859(JP,A) (58)調査した分野(Int.Cl.6,DB名) H01M 4/22,2/38,10/12 ────────────────────────────────────────────────── ─── Continuation of the front page (72) The inventor Isami Nagata 1006 Kazuma Kadoma, Kadoma City, Osaka Prefecture Matsushita Electric Industrial Co., Ltd. (56) References JP-A-57-124859 (JP, A) (58) Field (Int.Cl. 6 , DB name) H01M 4 / 22,2 / 38,10 / 12

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 比重が1.180以下の希硫酸を電槽化
成前に注液し、電槽化成終了後に電池を反転させて脱液
した後、比重1.400以下の硫酸を注入して再充電
し、電気分解によるガス発生によって前記脱液後の電池
内部に残存する低濃度電解液と脱液後に加えた高濃度電
解液とを攪拌して、所定の電解液比重とする電槽化成方
法において、その再充電が通電と通電の間に2秒以上1
0秒以下の休止を入れるサイクル充電であることを特徴
とする鉛蓄電池の電槽化成方法。
1. A specific gravity was injected before battery container Kasei 1.180 following dilute sulfuric acid, after draining by inverting the battery after the battery container conversion completion, by injecting specific gravity 1.400 or less of sulfuric acid The battery is recharged, and a low-concentration electrolytic solution remaining inside the battery after the liquid is removed by the gas generation due to electrolysis and a high-concentration electrolytic solution added after the liquid removal are stirred to form a specific electrolytic solution specific gravity. In the method, the recharging is performed for two seconds or more between energizations.
A method of forming a battery case for a lead-acid battery, wherein the battery is cycle-charged with a pause of 0 second or less.
JP3111604A 1991-05-16 1991-05-16 Battery storage method for lead-acid batteries Expired - Fee Related JP2982368B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3111604A JP2982368B2 (en) 1991-05-16 1991-05-16 Battery storage method for lead-acid batteries

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3111604A JP2982368B2 (en) 1991-05-16 1991-05-16 Battery storage method for lead-acid batteries

Publications (2)

Publication Number Publication Date
JPH04341759A JPH04341759A (en) 1992-11-27
JP2982368B2 true JP2982368B2 (en) 1999-11-22

Family

ID=14565560

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3111604A Expired - Fee Related JP2982368B2 (en) 1991-05-16 1991-05-16 Battery storage method for lead-acid batteries

Country Status (1)

Country Link
JP (1) JP2982368B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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

Also Published As

Publication number Publication date
JPH04341759A (en) 1992-11-27

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