JP2794588B2 - Sealed lead-acid battery - Google Patents
Sealed lead-acid batteryInfo
- Publication number
- JP2794588B2 JP2794588B2 JP1035523A JP3552389A JP2794588B2 JP 2794588 B2 JP2794588 B2 JP 2794588B2 JP 1035523 A JP1035523 A JP 1035523A JP 3552389 A JP3552389 A JP 3552389A JP 2794588 B2 JP2794588 B2 JP 2794588B2
- Authority
- JP
- Japan
- Prior art keywords
- battery
- electrode plate
- sealed lead
- granulated
- powder
- 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
Links
- 239000002253 acid Substances 0.000 title claims description 15
- 239000000843 powder Substances 0.000 claims description 22
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 20
- 239000003792 electrolyte Substances 0.000 claims description 11
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 10
- 239000000377 silicon dioxide Substances 0.000 claims description 10
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 2
- 229910001882 dioxygen Inorganic materials 0.000 claims description 2
- 238000000034 method Methods 0.000 claims 1
- 239000007789 gas Substances 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 4
- 238000002955 isolation Methods 0.000 description 4
- 239000008151 electrolyte solution Substances 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229910014474 Ca-Sn Inorganic materials 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000011164 primary particle Substances 0.000 description 1
- 239000011163 secondary particle Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
Landscapes
- Secondary Cells (AREA)
Description
【発明の詳細な説明】 産業上の利用分野 本発明は密閉式鉛蓄電池の改良に関するものである。Description: TECHNICAL FIELD The present invention relates to an improvement in a sealed lead-acid battery.
従来の技術とその課題 電池の充電中に発生する酸素ガスを負極で吸収させる
タイプの密閉式鉛蓄電池にはリテーナ式とゲル式の二種
類がある。リテーナ式は正極板と負極板との間に微細ガ
ラス繊維を素材とするマット状のセパレータ(ガラスセ
パレータ)を挿入し、これによって放電に必要な硫酸電
解液の保持と両極の隔離を行っており、近年、ポータブ
ル機器やコンピューターのバックアップ電源として広く
用いられるようになってきた。しかし、リテーナ式はガ
ラスセパレータが高価なことおよび充分な量の電解液を
保持できないために、低率放電では放電容量が電解液量
で制限されるという欠点があり、この種の密閉電池の普
及に障害となっている。2. Description of the Related Art There are two types of sealed lead-acid batteries of a type in which oxygen gas generated during charging of a battery is absorbed by a negative electrode, a retainer type and a gel type. In the retainer type, a mat-shaped separator (glass separator) made of fine glass fiber is inserted between the positive electrode plate and the negative electrode plate, thereby holding the sulfuric acid electrolyte required for discharge and isolating both electrodes. In recent years, it has been widely used as a backup power supply for portable devices and computers. However, the retainer type has the disadvantage that the discharge capacity is limited by the amount of electrolyte at low rate discharge because the glass separator is expensive and cannot hold a sufficient amount of electrolyte. Has become an obstacle.
一方、ゲル式はリテーナ式よりも安価であるが、電池
性能が液式やリテーナ式に劣るという欠点があった。On the other hand, the gel type is less expensive than the retainer type, but has a drawback that the battery performance is inferior to the liquid type and the retainer type.
そこで本発明は上述した従来の密閉式鉛蓄電池の欠点
を除去し、優れた放電性能を有する安価な密閉式鉛蓄電
池を提供するために電池の充放電に必要かつ充分な量の
硫酸電解液を、極板群の周囲に充填配置した、シリカ微
小粉体をバインダーを用いて造粒した多孔体の粉体に含
浸,保持させた密閉式鉛蓄電池を提案した。このタイプ
の密閉式鉛蓄電池において、実験を進めるうちにいくつ
かの欠点が明らかになった。すなわち (1)造粒粉体に電解液を含浸,保持させるため、注液
に長時間を要する。Therefore, the present invention eliminates the above-mentioned disadvantages of the conventional sealed lead-acid battery, and provides a necessary and sufficient amount of sulfuric acid electrolyte for charging and discharging the battery in order to provide an inexpensive sealed lead-acid battery having excellent discharge performance. We have proposed a sealed lead-acid battery in which a porous silica powder filled and arranged around an electrode group is impregnated and held in a porous powder granulated using a binder. Several shortcomings became apparent during the course of experiments with this type of sealed lead-acid battery. That is, (1) it takes a long time to inject the liquid for impregnating and holding the electrolyte in the granulated powder.
(2)充電中に発生するガスのために造粒粉体が移動し
てガス溜りが生じやすい。また、電解液がガスにより押
し出されて電槽外部にあふれる。(2) Due to the gas generated during charging, the granulated powder moves and gas accumulation is likely to occur. Further, the electrolytic solution is pushed out by the gas and overflows outside the battery case.
という欠点がある。There is a disadvantage that.
課題を解決するための手段 本発明は上述した造粒粉体に硫酸電解液を含浸保持さ
せてなる密閉式鉛蓄電池の欠点を除去するもので、その
骨子とするところは電槽内側面の少くとも1面に多孔性
シートを当接することにある。以下本発明を実施例に基
づいて説明する。Means for Solving the Problems The present invention is to eliminate the drawbacks of the sealed lead-acid battery obtained by impregnating and holding the above-described granulated powder with a sulfuric acid electrolyte, and the main point is that the inner surface of the battery case has a small area. In both cases, the porous sheet is brought into contact with one surface. Hereinafter, the present invention will be described based on examples.
実施例 Pb−Ca−Sn合金より成る正および負極格子体に通常の
正極および負極ペーストをそれぞれ充填した後、熟成を
施して未化成極板を作製した。ついでこれらの正極およ
び負極未化成極板を用い、第1図に示す隔離棒を両極板
の間に挿入して極板群を作製した。図に示す隔離棒1は
耐酸性の合成樹脂をE字形に成形したもので、鉛直方向
の隔離棒には波形2をつけてある。この極板群を電槽に
挿入すると共にあらかじめ電槽の短側面の内側、ここで
は極板の側部に当たる内面2面に多孔性シートとしてガ
ラスマットを当接した。ここで多孔性シートとしては造
粒粉体が浸入しにくくかつガスおよび液体の透過性の良
好な耐酸性を有するものであればよい。Example The positive and negative electrode grids made of a Pb-Ca-Sn alloy were each filled with ordinary positive and negative electrode pastes and then aged to produce an unformed electrode plate. Next, using these positive electrode and negative electrode non-polarized electrode plates, an isolation rod shown in FIG. 1 was inserted between the two electrode plates to prepare an electrode plate group. The isolation bar 1 shown in the figure is formed by molding an acid-resistant synthetic resin into an E-shape, and the vertical isolation bar is corrugated. The electrode plate group was inserted into the battery case, and a glass mat as a porous sheet was previously brought into contact with the inside of the short side surface of the battery case, in this case, two inner surfaces corresponding to the side portions of the electrode plate. Here, any porous sheet may be used as long as it is hard to penetrate the granulated powder and has good acid resistance with good gas and liquid permeability.
こののち電槽と極板群の隙間および極板間の隙間に電
解液の保持体を充填する。この電解液保持体は次のよう
に調製した。まず、粒径が10〜40ミリミクロンの微小シ
リカ粉体を、バインダーとしてメタアクリル酸メチルを
15%加えて水で練合し、ついで粒径を100〜200ミクロン
に造粒した後乾燥した。造粒シリカ粉体はシリカ微小一
次粒子が凝集して100〜200ミクロンの二次粒子となって
おり、造粒粉体自身の気孔率は85%以上のさらさらした
粉体である。Thereafter, a gap between the battery case and the electrode plate group and a gap between the electrode plates are filled with an electrolyte holder. This electrolyte holder was prepared as follows. First, a fine silica powder having a particle size of 10 to 40 millimicrons and methyl methacrylate as a binder
15% was added and kneaded with water, then granulated to a particle size of 100 to 200 microns and dried. The granulated silica powder is formed by agglomeration of silica fine primary particles into secondary particles of 100 to 200 microns, and the granulated powder itself is a free-flowing powder having a porosity of 85% or more.
造粒シリカ粉体を充填した状態を第2図に示す。 FIG. 2 shows a state in which the granulated silica powder is filled.
シリカ粉体は電池に振動を加えながら充填した。図に
示したように造粒シリカ粉体は、極板群の周囲および極
板間に密につまっていた。ここで極板間に充填した造粒
シリカ粉体はセパレータの機能も有している。造粒シリ
カ粉体を充填後はフタを接着し排気弁を装着した。充填
状態での気孔率は約90%であった。The silica powder was filled while applying vibration to the battery. As shown in the figure, the granulated silica powder was densely packed around the electrode group and between the electrode plates. Here, the granulated silica powder filled between the electrode plates also has the function of a separator. After filling the granulated silica powder, the lid was adhered and an exhaust valve was attached. The porosity in the filled state was about 90%.
次に試作電池に硫酸電解液を注入した。供試電池は公
称容量4.5Ahで、比較のために同じロットの正極および
負極板を用いて、電槽内側面に多孔性シートを配置せず
に造粒粉体を充填した密閉式鉛蓄電池(比較品1)およ
び従来のリテーナ式電池(比較品2)についても製作し
試験した。その結果を第1表に示す。Next, a sulfuric acid electrolyte was injected into the prototype battery. The test battery has a nominal capacity of 4.5 Ah. For comparison, a sealed lead-acid battery (filled with granulated powder without using a porous sheet on the inner surface of the battery case, using positive and negative plates of the same lot for comparison) A comparative product 1) and a conventional retainer type battery (comparative product 2) were also manufactured and tested. Table 1 shows the results.
第1表から明らかなように本発明品は従来のリテーナ
式電池(比較品2)とほぼ同じ程度の時間で電解液を注
入することができ、電槽内側面に多孔性シートを配置し
なかったもの(比較品1)に比べ1/10の時間に短縮でき
た。また、電池性能は第2表に示すようにリテーナ式電
池に比べ大幅に改善することができた。As is clear from Table 1, the product of the present invention can inject the electrolytic solution in substantially the same time as the conventional retainer type battery (comparative product 2), and does not arrange a porous sheet on the inner surface of the battery case. The time was reduced to 1/10 of that of the product (Comparative Product 1). Also, as shown in Table 2, the battery performance was significantly improved as compared with the retainer type battery.
また充電中に発生するガスは極板側部より多孔性シー
トを介して密閉反応に寄与するようになるため、造粒粉
体を押し上げたりガス溜りを形成したりすることが少な
くなった。 Further, the gas generated during charging comes to contribute to the hermetic reaction from the side of the electrode plate through the porous sheet, and therefore, it is less likely to push up the granulated powder or to form a gas reservoir.
ここで用いた多孔性シートは極板側部の2面にのみ当
接したが、少くとも1面に多孔性シートを当接すれば効
果が認められた。また、充填した造粒粉体の上部に多孔
性シートを配置することも有効であった。Although the porous sheet used here was in contact only with two surfaces on the side of the electrode plate, an effect was recognized when the porous sheet was in contact with at least one surface. It was also effective to arrange a porous sheet above the filled granulated powder.
発明の効果 上述の実施例から明らかなように電池内に充填したシ
リカ微粉体の造粒粉体によって電解質の保持および正,
負極板の隔離を行った密閉式鉛蓄電池において電槽側面
に多孔性シートを当接することにより電解液の注入時間
を大幅に短縮すると共に電池性能を改善できた点工業的
価値は非常に大きい。Effect of the Invention As is clear from the above-described embodiment, the retention of the electrolyte and the positive and negative
In a sealed lead-acid battery in which a negative electrode plate is isolated, contacting a porous sheet to the side surface of a battery case significantly reduces the time for injecting an electrolytic solution and improves battery performance.
第1図は隔離棒の斜視図、第2図は本発明による密閉式
鉛蓄電池の横断面図である。 1……隔離棒、3……電槽、4……負極板、5……正極
板、6……造粒粉体FIG. 1 is a perspective view of an isolation rod, and FIG. 2 is a cross-sectional view of a sealed lead-acid battery according to the present invention. DESCRIPTION OF SYMBOLS 1 ... Separating rod, 3 ... Battery case, 4 ... Negative electrode plate, 5 ... Positive electrode plate, 6 ... Granulated powder
───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 昭57−65677(JP,A) 特開 昭61−198573(JP,A) (58)調査した分野(Int.Cl.6,DB名) H01M 10/10 - 10/12────────────────────────────────────────────────── ─── Continuation of the front page (56) References JP-A-57-65677 (JP, A) JP-A-61-198573 (JP, A) (58) Fields investigated (Int. Cl. 6 , DB name) H01M 10/10-10/12
Claims (1)
吸収させる密閉式鉛蓄電池において、正極板と負極板と
の間を一定の間隔に保持してなる極板群を電槽内に収納
すると共に、電槽内側面の少くとも1面に多孔性シート
を当接配置し、正極板と負極板との間隙および極板群の
周囲に10〜40ミリミクロンのシリカ微小粉体をバインダ
ーを用いて造粒した多孔性の粉体を充填,配置し、放電
に必要かつ充分な量の硫酸電解液を上記造粒粉体に含
浸,保持させることを特徴とする密閉式鉛蓄電池。In a sealed lead-acid battery in which oxygen gas generated during charging of a battery is absorbed by a negative electrode, a group of electrode plates having a predetermined interval between a positive electrode plate and a negative electrode plate is placed in a battery case. At the same time, a porous sheet is placed in contact with at least one of the inner surfaces of the battery case, and a silica fine powder of 10 to 40 millimicrons is bound around the gap between the positive electrode plate and the negative electrode plate and around the electrode group. A sealed lead-acid battery characterized by filling and arranging a porous powder granulated by using the above method, and impregnating and holding the granulated powder with a sufficient amount of a sulfuric acid electrolyte necessary for discharge.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1035523A JP2794588B2 (en) | 1989-02-15 | 1989-02-15 | Sealed lead-acid battery |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1035523A JP2794588B2 (en) | 1989-02-15 | 1989-02-15 | Sealed lead-acid battery |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02215056A JPH02215056A (en) | 1990-08-28 |
JP2794588B2 true JP2794588B2 (en) | 1998-09-10 |
Family
ID=12444109
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1035523A Expired - Fee Related JP2794588B2 (en) | 1989-02-15 | 1989-02-15 | Sealed lead-acid battery |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2794588B2 (en) |
-
1989
- 1989-02-15 JP JP1035523A patent/JP2794588B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JPH02215056A (en) | 1990-08-28 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
LAPS | Cancellation because of no payment of annual fees |