JP2001185203A - Manufacturing method of sealed type lead-acid battery - Google Patents

Manufacturing method of sealed type lead-acid battery

Info

Publication number
JP2001185203A
JP2001185203A JP37188999A JP37188999A JP2001185203A JP 2001185203 A JP2001185203 A JP 2001185203A JP 37188999 A JP37188999 A JP 37188999A JP 37188999 A JP37188999 A JP 37188999A JP 2001185203 A JP2001185203 A JP 2001185203A
Authority
JP
Japan
Prior art keywords
battery
sulfuric acid
granular silica
solution
silica
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
JP37188999A
Other languages
Japanese (ja)
Inventor
Masashi Adachi
昌司 足立
Yasutaka Doyama
堂山  泰隆
Toshiki Yoshioka
俊樹 吉岡
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.)
Japan Storage Battery Co Ltd
Original Assignee
Japan Storage Battery 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 Japan Storage Battery Co Ltd filed Critical Japan Storage Battery Co Ltd
Priority to JP37188999A priority Critical patent/JP2001185203A/en
Publication of JP2001185203A publication Critical patent/JP2001185203A/en
Pending legal-status Critical Current

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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

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  • Secondary Cells (AREA)

Abstract

PROBLEM TO BE SOLVED: To provide a manufacturing method of lead-acid battery having superior productivity and battery performance, in the case where a solution in which granular silica and dilute sulfuric acid are dispersed is injected into the battery, and where only excess electrolyte is discharged from a drain hole. SOLUTION: In this manufacturing method of granular type sealed lead-acid battery where a solution in which granular silica is dispersed in dilute sulfuric acid s injected from the inlet of the battery and the excess dilute sulfuric acid in the battery from drain hole, where the filling of granular silica and injection of sulfuric acid are carried out simultaneously, the concentration of granular silica and dilute sulfuric acid in the dispersed solution is granular silica/sulfuric acid=0.15-0.25 g/cc.

Description

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

【0001】[0001]

【発明の属する技術分野】本発明は密閉形鉛蓄電池の製
造方法に関する。
[0001] The present invention relates to a method for manufacturing a sealed lead-acid battery.

【0002】[0002]

【従来の技術】従来から、密閉形鉛蓄電池の液保持方式
として、電解液を微細ガラス繊維からなるマット状のセ
パレータに電解液を含浸・保持させる、いわゆるリテー
ナ式がある。この方式の電池は、初期容量は良いが、セ
パレータが活物質を圧迫する力が弱く、活物質の劣化や
格子の伸びなどにより寿命性能が早期に低下すると言う
問題点がある。
2. Description of the Related Art There has been a so-called retainer type in which an electrolyte is impregnated and held in a mat-like separator made of fine glass fibers as an electrolyte as a liquid holding system for a sealed lead-acid battery. The battery of this type has a good initial capacity, but has a problem in that the separator has a weak force to press the active material, and the life performance deteriorates early due to the deterioration of the active material and the expansion of the lattice.

【0003】このため、近年、顆粒状シリカを極板間お
よび極板群の周囲に密に充填して、極板、セパレータお
よび顆粒シリカに電解液を保持させる、顆粒シリカ式電
池が提案されている。これにより、電池内に密に充填し
たシリカが極板を全方向から圧迫するため、寿命性能は
著しく改善される。
For this reason, in recent years, there has been proposed a granular silica battery in which granular silica is densely filled between the electrodes and around the electrode group so that the electrode plate, the separator and the granular silica retain an electrolyte. I have. As a result, the silica that is densely filled in the battery presses the electrode plate from all directions, so that the life performance is significantly improved.

【0004】たとえば、公開特許公報特開平3−252
063には、電池に直径が10〜500μmのシリカ粉
体を充填して、極板、セパレータおよびシリカ粉体に電
解液を保持させた密閉形鉛蓄電池が記載されている。し
かもシリカ粉体は従来のガラス繊維セパレータに比べ非
常に安価な材料であり、安価で性能の優れた電池を可能
にする重要な材料であると言える。
For example, Japanese Patent Laid-Open Publication No. Hei 3-252
No. 063 describes a sealed lead-acid battery in which a battery is filled with silica powder having a diameter of 10 to 500 μm, and an electrode plate, a separator, and an electrolyte are held in the silica powder. Moreover, silica powder is a very inexpensive material as compared with conventional glass fiber separators, and can be said to be an important material that enables batteries that are inexpensive and have excellent performance.

【0005】[0005]

【発明が解決しようとする課題】電池の電解液保持材に
用いるシリカ粉体は、できるだけ多量の電解液を保持さ
せることが必要であるので、多孔質なシリカを用いてい
る。シリカを多孔質にすると、シリカの流動性が悪くな
り、電池内への充填は振動機により強い振動を与える必
要がある。
As the silica powder used for the electrolyte holding material of the battery, it is necessary to hold as much electrolyte as possible, so porous silica is used. When the silica is made porous, the fluidity of the silica deteriorates, and it is necessary to give strong vibration to the filling of the battery with a vibrator.

【0006】またそのようなシリカ粉体は比表面積が高
く、電解液を注液するにも電池内を真空ポンプにより減
圧状態にして注液する減圧注液が必要である。従って、
振動機や減圧注液装置など設備費が高くなることや、顆
粒充填、注液にかなりの時間を要するなど、生産性が低
く製造コストが高くなるという欠点があった。
Further, such a silica powder has a high specific surface area, and it is necessary to apply a reduced-pressure injection in which the inside of the battery is reduced by a vacuum pump in order to inject the electrolytic solution. Therefore,
There are drawbacks such as high equipment costs such as a vibrator and a reduced pressure injection device, and considerable time required for filling and injecting granules, resulting in low productivity and high production cost.

【0007】このため、振動充填と真空注液を一つの工
程にするために、側面あるいは底面に穴とそれを覆うフ
ィルターを設けた電槽を用いた未注液電池に、顆粒シリ
カと希硫酸を分散させた溶液を注液し、排出口から余剰
電解液のみを排出する製造方法がある(公開特許公報特
開平7−122288)。この製造方法においても余剰
電解液排出速度が著しく遅くなる場合があり、かえって
製造費が高くなってしまうこともあった。なおかつ、排
出速度が遅い電池は電池容量が不足し、電池性能にまで
悪影響を及ぼす場合があった。
For this reason, in order to combine vibration filling and vacuum injection into one process, an uninjected battery using a battery case provided with a hole on the side or bottom surface and a filter for covering the hole is provided with granular silica and diluted sulfuric acid. There is a production method in which a solution in which is dispersed is injected, and only the surplus electrolytic solution is discharged from a discharge port (Japanese Patent Application Laid-Open No. 7-122288). Also in this manufacturing method, the discharge rate of the surplus electrolyte may be extremely slow, and the manufacturing cost may be rather increased. In addition, a battery having a low discharge rate has a shortage of battery capacity, which may adversely affect battery performance.

【0008】本発明が解決しようとする課題は、顆粒シ
リカと希硫酸を分散させた溶液を注液し、排出口から余
剰電解液のみを排出する場合において、生産性と電池性
能の優れた密閉形鉛蓄電池の製造方法を提供することで
ある。
[0008] The problem to be solved by the present invention is that when a solution in which granular silica and dilute sulfuric acid are dispersed is injected and only the surplus electrolyte is discharged from the discharge port, a sealed package having excellent productivity and battery performance is obtained. An object of the present invention is to provide a method for manufacturing a lead-acid battery.

【0009】[0009]

【課題を解決するための手段】上記課題を解決するため
に、請求項1記載の発明の密閉形鉛蓄電池の製造方法で
は、顆粒シリカを希硫酸に分散させた溶液を、電池の注
液口から注液し、排出口から電池内の余剰の希硫酸を排
出させて顆粒シリカの充填と硫酸の注液とを同時に行な
う顆粒式密閉形鉛蓄電池の製造方法において、電池に注
入する顆粒シリカと希硫酸の分散溶液濃度が顆粒シリカ
/硫酸=0.15〜0.25g/ccであることを特徴
とする。
According to a first aspect of the present invention, there is provided a method of manufacturing a sealed lead-acid battery according to the first aspect of the present invention, comprising the steps of: In the method for producing a granular sealed lead-acid battery, in which the excess diluted sulfuric acid in the battery is discharged from the outlet and the filling of the granular silica and the injection of sulfuric acid are simultaneously performed, the granular silica to be injected into the battery and It is characterized in that the concentration of the dilute sulfuric acid dispersion solution is granular silica / sulfuric acid = 0.15 to 0.25 g / cc.

【0010】[0010]

【発明の実施の形態】以下に、本発明の好ましい実施の
形態を説明するが、本発明は以下の説明に限定されるも
のではない。
DESCRIPTION OF THE PREFERRED EMBODIMENTS Preferred embodiments of the present invention will be described below, but the present invention is not limited to the following description.

【0011】本発明による密閉形鉛蓄電池の製造方法
は、顆粒シリカを希硫酸に分散させた溶液を、電池の注
液口から注液し、他面の排出口から電池内の余剰の希硫
酸を排出させて顆粒シリカの充填と硫酸の注液とを同時
に行なう顆粒式密閉形鉛蓄電池の製造方法において、電
池の注入する顆粒シリカと希硫酸の分散溶液濃度が顆粒
シリカ/硫酸=0.15〜0.25g/ccであること
である。
[0011] In the method for manufacturing a sealed lead-acid battery according to the present invention, a solution in which granular silica is dispersed in diluted sulfuric acid is injected from an inlet of the battery, and excess diluted sulfuric acid in the battery is discharged from an outlet on the other surface. , And the filling of granular silica and the injection of sulfuric acid are carried out simultaneously, and the concentration of the dispersed solution of granular silica and dilute sulfuric acid to be injected into the battery is such that the ratio of granular silica / sulfuric acid = 0.15 0.20.25 g / cc.

【0012】顆粒シリカと希硫酸の分散液濃度が顆粒シ
リカ/硫酸=0.15〜0.25g/ccの範囲内にで
ある場合には、電池への注入が早く完了し、かつ余剰の
希硫酸排出を著しく早くすることができるため、電池製
造コストを大幅に低減することができる。
When the concentration of the dispersion of granular silica and diluted sulfuric acid is in the range of 0.15 to 0.25 g / cc of granular silica / sulfuric acid, the injection into the battery is completed quickly and the excess diluted sulfuric acid is added. Since sulfuric acid discharge can be remarkably accelerated, battery manufacturing costs can be significantly reduced.

【0013】さらに、余剰希硫酸排出後の電池内電解液
分布が均一になるため、良好な電池性能を安定して得る
ことができる。
Furthermore, since the distribution of the electrolyte solution in the battery after discharging the excess diluted sulfuric acid becomes uniform, good battery performance can be stably obtained.

【0014】[0014]

【実施例】以下、本発明を実施例に基づいて説明する。DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be described below with reference to embodiments.

【0015】まず、未化成のペースト式正、負極板およ
び合成樹脂性のセパレータからなる極板群を、底部にシ
リカの通らないフィルターの付いた排出口を設けた電槽
に挿入し、蓋の溶着を行なった。
First, a group of electrodes consisting of unformed paste-type positive and negative electrodes and a separator made of a synthetic resin is inserted into a battery case provided with an outlet having a filter through which silica does not pass. Welding was performed.

【0016】その後、図1に示すように、平均粒子径約
60μm(コールターカウンター法で測定)の顆粒シリ
カを比重1.31(20℃)の希硫酸に加えた顆粒シリ
カ分散希硫酸溶液5をホッパー7を通して電池の蓋2に
設けた注入口6から注入した。
Thereafter, as shown in FIG. 1, a granular silica-dispersed dilute sulfuric acid solution 5 was prepared by adding granular silica having an average particle size of about 60 μm (measured by a Coulter counter method) to dilute sulfuric acid having a specific gravity of 1.31 (20 ° C.). Injection was performed through an injection port 6 provided in the battery lid 2 through a hopper 7.

【0017】溶液の濃度は顆粒シリカ/硫酸=0.10
0g/cc(A)、0.125g/cc(B)、0.1
50g/cc(C)、0.175g/cc(D)、0.
200g/cc(E)、0.225g/cc(F)、
0.250g/cc(G)、0.275g/cc(H)
とした。底部の排出口4から真空ポンプ8で減圧して余
剰の希硫酸を抜きながら、電池内に顆粒シリカの充填と
電解液の注液とを同時に行なった後、電池底部の排出口
4を熱溶着により気密に封口して、定格容量60Ah
(3hR)−2Vの電池を製作した。
The concentration of the solution is granular silica / sulfuric acid = 0.10
0 g / cc (A), 0.125 g / cc (B), 0.1
50 g / cc (C), 0.175 g / cc (D), 0.
200 g / cc (E), 0.225 g / cc (F),
0.250 g / cc (G), 0.275 g / cc (H)
And After filling the inside of the battery with granular silica and injecting the electrolytic solution at the same time while removing excess dilute sulfuric acid by reducing the pressure with the vacuum pump 8 from the outlet 4 at the bottom, the outlet 4 at the bottom of the battery is thermally welded. Sealed more airtight, rated capacity 60Ah
A (3hR) -2V battery was produced.

【0018】いずれの電池も、所定量の充電を行って、
電解液比重が1.32(20℃)になるようにし、充電
後は常法にしたがって、安全弁を装着した。
Each of the batteries is charged with a predetermined amount,
The specific gravity of the electrolyte was adjusted to 1.32 (20 ° C.), and after charging, a safety valve was attached according to a conventional method.

【0019】電解液の排出に要した時間を表1に示す。
分散溶液濃度が0.15g/ccより薄い場合には所用
時間が7分以上と長時間を要するが、0.15〜0.2
5g/ccの場合には2〜4分と短時間であり、分散液
濃度の濃いほうが短時間であった。
Table 1 shows the time required for discharging the electrolyte.
When the concentration of the dispersion solution is lower than 0.15 g / cc, the required time is as long as 7 minutes or more.
In the case of 5 g / cc, the time was as short as 2 to 4 minutes, and the higher the dispersion concentration, the shorter the time.

【0020】しかし、0.25g/ccをより濃くなる
と、分散溶液の流動性が失われ、電池内への注液が不可
能であった。なお、所用時間は各電池10個の製作所用
時間の平均値である。
However, when the concentration was increased to 0.25 g / cc, the fluidity of the dispersion solution was lost, and it was impossible to inject the solution into the battery. The required time is an average value of the time required for the manufacturing of ten batteries.

【0021】[0021]

【表1】 [Table 1]

【0022】なお、余剰電解液排出後の分散溶液濃度
は、注入時よりも小さくなる。その値は電池の構成によ
って変わってくるが、本実施例の本発明品では、硫酸(c
c)/顆粒シリカ(g)が2.20〜2.60cc/gであ
った。さらに充電完了後の分散溶液濃度はそれよりもさ
らに小さくなり、これも電池の構成により変わるが本実
施例の本発明品では、硫酸(cc)/顆粒シリカ(g)が2.
18〜2.58cc/gであり、いずれも問題なかっ
た。注液後の分散溶液濃度は電池の構成により数値が変
わるが、注入時点の分散溶液濃度は、電池の構成が変わ
っても本発明の範囲内であれば良い。
Note that the concentration of the dispersion solution after the discharge of the surplus electrolytic solution is smaller than that at the time of injection. Although the value varies depending on the configuration of the battery, the sulfuric acid (c
c) / granular silica (g) was 2.20 to 2.60 cc / g. Further, the concentration of the dispersion solution after the completion of charging is further lower than that, which also depends on the configuration of the battery, but in the present invention product of this embodiment, the sulfuric acid (cc) / granular silica (g) is 2.
It was 18 to 2.58 cc / g, and there was no problem in any case. Although the numerical value of the concentration of the dispersion solution after the injection varies depending on the configuration of the battery, the concentration of the dispersion solution at the time of injection may be within the range of the present invention even if the configuration of the battery changes.

【0023】上述の電池を10hR電流で1.7Vまで
放電し、10hR電流で放電量の135%の充電を行う
サイクルを10回繰り返し、10サイクル目の容量で電
池の性能を評価した。試験結果を表2に示す。本発明の
電池の容量は濃度の薄い分散溶液を用いた電池のそれよ
りも約4%多かった。分散溶液濃度の薄い電池の容量が
少ないのは、電解液の注液に時間がかかることからも予
想されるように、電解液が電池全体に均一に分布してお
らず、反応分布が不均一になっているためと思われる。
一方、本発明の電池はそれと逆に電解液の分布がより均
一化しているものと思われる。
The above battery was discharged at a current of 10 hR to 1.7 V and a cycle of charging at 135% of the discharged amount at a current of 10 hR was repeated ten times, and the performance of the battery was evaluated at the capacity of the tenth cycle. Table 2 shows the test results. The capacity of the battery of the present invention was about 4% higher than that of the battery using the dilute dispersion solution. The low capacity of a battery with a low concentration of the dispersion solution is not uniform because the electrolyte is not uniformly distributed throughout the battery, as expected from the fact that it takes time to inject the electrolyte. It seems to be because.
On the other hand, it seems that the battery of the present invention has a more uniform distribution of the electrolytic solution.

【0024】[0024]

【表2】 [Table 2]

【0025】なお、排出口を底面に設けたが、電槽側面
に設けても同様の効果を示した。
Although the outlet is provided on the bottom surface, the same effect can be obtained by providing the outlet on the side of the battery case.

【0026】[0026]

【発明の効果】以上述べたように、本発明の密閉形鉛蓄
電池の製造方法は従来の製造方法に比べ、得られた密閉
形鉛蓄電池の電池性能が優れておりかつ生産性に優れて
おり、その工業的価値はきわめて大きい。
As described above, the method for producing a sealed lead-acid battery of the present invention is superior to the conventional production method in that the obtained sealed lead-acid battery has excellent battery performance and excellent productivity. , Its industrial value is extremely large.

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

【図1】 本発明による顆粒式密閉鉛蓄電池製造方法を
示す模式図
FIG. 1 is a schematic view showing a method for producing a granular sealed lead-acid battery according to the present invention.

【符号の説明】 1 電池 2 蓋 3 フィルター 4 排出口 5 顆粒シリカ分散希硫酸溶液 6 注入口 7 ホッパー 8 真空ポンプ 9 排出希硫酸[Description of Signs] 1 Battery 2 Lid 3 Filter 4 Outlet 5 Granular silica dispersed diluted sulfuric acid solution 6 Inlet 7 Hopper 8 Vacuum pump 9 Discharged diluted sulfuric acid

フロントページの続き Fターム(参考) 5H028 AA01 AA06 BB02 BB03 HH02 HH03 Continued on the front page F term (reference) 5H028 AA01 AA06 BB02 BB03 HH02 HH03

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】顆粒シリカを希硫酸に分散させた溶液を、
電池の注液口から注液し、排出口から電池内の余剰の希
硫酸を排出させて顆粒シリカの充填と硫酸の注液とを同
時に行なう顆粒式密閉形鉛蓄電池の製造方法において、
電池に注入する顆粒シリカと希硫酸の分散溶液濃度が顆
粒シリカ/硫酸=0.15〜0.25g/ccであるこ
とを特徴とする密閉形鉛蓄電池の製造方法。
1. A solution in which granular silica is dispersed in dilute sulfuric acid,
Injection from the injection port of the battery, discharging the excess dilute sulfuric acid in the battery from the outlet, filling the granular silica and injecting sulfuric acid at the same time, the method of manufacturing a granular sealed lead-acid battery,
A method for producing a sealed lead-acid battery, wherein the concentration of a dispersion of granular silica and dilute sulfuric acid to be injected into the battery is from 0.15 to 0.25 g / cc of granular silica / sulfuric acid.
JP37188999A 1999-12-27 1999-12-27 Manufacturing method of sealed type lead-acid battery Pending JP2001185203A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP37188999A JP2001185203A (en) 1999-12-27 1999-12-27 Manufacturing method of sealed type lead-acid battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP37188999A JP2001185203A (en) 1999-12-27 1999-12-27 Manufacturing method of sealed type lead-acid battery

Publications (1)

Publication Number Publication Date
JP2001185203A true JP2001185203A (en) 2001-07-06

Family

ID=18499480

Family Applications (1)

Application Number Title Priority Date Filing Date
JP37188999A Pending JP2001185203A (en) 1999-12-27 1999-12-27 Manufacturing method of sealed type lead-acid battery

Country Status (1)

Country Link
JP (1) JP2001185203A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114050328A (en) * 2021-11-17 2022-02-15 骆驼集团华中蓄电池有限公司 Preparation method of SLI parking air conditioner battery

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114050328A (en) * 2021-11-17 2022-02-15 骆驼集团华中蓄电池有限公司 Preparation method of SLI parking air conditioner battery
CN114050328B (en) * 2021-11-17 2024-05-17 骆驼集团华中蓄电池有限公司 Preparation method of SLI parking air conditioner battery

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