JPH0654680B2 - Sealed lead acid battery - Google Patents
Sealed lead acid batteryInfo
- Publication number
- JPH0654680B2 JPH0654680B2 JP63312181A JP31218188A JPH0654680B2 JP H0654680 B2 JPH0654680 B2 JP H0654680B2 JP 63312181 A JP63312181 A JP 63312181A JP 31218188 A JP31218188 A JP 31218188A JP H0654680 B2 JPH0654680 B2 JP H0654680B2
- Authority
- JP
- Japan
- Prior art keywords
- battery
- sealed lead
- electrode plate
- acid battery
- negative electrode
- 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
Classifications
-
- 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
- H01M10/34—Gastight accumulators
- H01M10/342—Gastight lead accumulators
-
- 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
- H01M10/08—Selection of materials as electrolytes
- H01M10/10—Immobilising of electrolyte
-
- 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
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。TECHNICAL FIELD The present invention relates to an improvement of 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。Conventional technology and its problems There are two types of sealed lead-acid batteries, the retainer type and the gel type, in which the negative electrode absorbs oxygen gas generated during charging of the battery. The retainer type inserts a mat-shaped separator (glass separator) made of fine glass fibers between the positive electrode plate and the negative electrode plate, thereby holding the sulfuric acid electrolyte necessary for discharge and separating the two electrodes. In recent years, it has been widely used as a backup power source for portable devices and computers. However, the retainer type has a drawback that the discharge capacity is limited by the amount of the electrolytic solution at low rate discharge because the glass separator is expensive and cannot hold a sufficient amount of the electrolytic solution. Is 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 that of the retainer type.
課題を解決するための手段 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
供するもので、その骨子とするところは電池の充放電に
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,保持させるところにある。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 eliminates the above-mentioned drawbacks of the conventional sealed lead-acid battery, and provides an inexpensive sealed lead-acid battery having excellent discharge performance. This is to impregnate and hold a sufficient amount of sulfuric acid electrolyte necessary for charging / discharging in a powder of a porous body in which silica fine powder is granulated using a binder, which is placed around the electrode plate group. The present invention will be described below 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充填した後、直径0.5 〜1.0 ミ
クロンの微細ガラス繊維を抄紙した厚み0.1 ミリのガラ
スペーパーを充填極板の両面に貼付した。その後正,負
極板とも熟成を施してから厚み0.5 ミリの低抵抗合成セ
パレータを用いて正極板3枚,負極板4枚構成の極板群
を作製し、電槽に挿入した。ついで粒径が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%加えて水で練合して粒径を100 〜20
0 ミクロンに造粒後乾燥したものを電槽壁と極板群との
間に振動を加えながら密に充填した。ここで充填した造
粒物はシリカの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、充填状態での気孔率は約
85%であった。また、造粒物自身の気孔率は90%以上で
あった。EXAMPLE A positive and negative electrode grid made of Pb-Ca-Sn alloy was filled with ordinary positive and negative electrode pastes, and then 0.1 mm thick glass paper made from fine glass fibers with a diameter of 0.5 to 1.0 micron was filled. Attached to both sides. After that, both the positive and negative electrode plates were aged, and then a positive electrode group consisting of three positive electrode plates and four negative electrode plates was prepared using a low resistance synthetic separator having a thickness of 0.5 mm, and was inserted into a battery case. Then, add 15% of methyl methacrylate as a binder to a fine silica powder with a particle size of 10-40 mm and knead with water to obtain a particle size of 100-20.
What was dried after being granulated to 0 micron was densely packed while applying vibration between the battery cell wall and the electrode plate group. The granules filled here are secondary particles of 100-200 microns that are formed by agglomeration of fine silica primary particles, and the porosity in the filled state is about
It was 85%. The porosity of the granulated product itself was 90% or more.
このようにして造粒物を充填した後フタを接着し、排気
弁を装着して公称容量4.5Ah の密閉式鉛蓄電池を作製
し、容量試験に供した。なお、比較のために同じロット
の極板を用いた従来のリテーナ式電池およびゲル式電池
も同時に試験した。第1表はその試験結果である。After filling the granulated material in this way, the lid was adhered, an exhaust valve was attached, and a sealed lead-acid battery having a nominal capacity of 4.5 Ah was produced and subjected to a capacity test. For comparison, a conventional retainer battery and gel battery using the same lot of electrode plates were also tested at the same time. Table 1 shows the test results.
この試験結果より、リテーナ式とゲル式とを比較する
と、リテーナ式は電解液比重がやや高いためにゲル式よ
りも高率放電性能が優れていた。一方、本発明品はこれ
ら従来の密閉式鉛蓄電池に比べて低率放電、高率放電と
も10〜20%も性能が向上した。これは電解液量がリテー
ナ式よりも多いこと、液比重をゲル式より高くしたこ
と、酸の拡散がリテーナ式やゲル式に比べて優れていた
ことおよび正極板と負極板の両面に貼付したガラスペー
パーが電解液の補給に有効に作用したことなどの相乗効
果であると思われる。 From this test result, when comparing the retainer type and the gel type, the retainer type was superior in high rate discharge performance to the gel type because the electrolytic solution specific gravity was slightly high. On the other hand, the product of the present invention has improved performance by 10 to 20% in both low rate discharge and high rate discharge as compared with these conventional sealed lead acid batteries. This was because the amount of electrolyte was larger than that of the retainer type, the specific gravity of the liquid was higher than that of the gel type, the diffusion of acid was better than that of the retainer type and gel type, and it was attached on both sides of the positive electrode plate and the negative electrode plate. It is believed that there is a synergistic effect such as the glass paper effectively acting to replenish the electrolyte.
ちなみに、極板表面にガラスペーパーを貼付しない電池
を試作して調べてみたところ、電池性能は従来品と同じ
程度であった。このことからも、ガラスペーパー貼付の
効果は明らかである。By the way, when a prototype of a battery in which glass paper was not attached to the surface of the electrode plate was prototyped and examined, the battery performance was about the same as the conventional product. From this, the effect of sticking the glass paper is clear.
発明の効果 上述の実施例から明らかなように、本発明による密閉式
鉛蓄電池は電解液の保持にシリカ微粉体の造粒物を用い
ると共に、極板の表面にガラスペーパーを貼付するとい
う簡単な操作で、従来の密閉式鉛蓄電池の放電性能を大
幅に改善できた点工業的価値は非常に大きい。EFFECTS OF THE INVENTION As is apparent from the above-described examples, the sealed lead-acid battery according to the present invention uses a granulated product of silica fine powder for holding the electrolytic solution, and a simple method of pasting glass paper on the surface of the electrode plate. The industrial value is extremely high in that the discharge performance of the conventional sealed lead-acid battery can be greatly improved by operation.
Claims (1)
吸収させる密閉式鉛蓄電池において、正極板および負極
板の両面に微細ガラス繊維より成る薄いガラスペーパー
を貼付した極板と低抵抗のセパレータとから構成される
極板群を電槽内に収納すると共に、この極板群の周囲に
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。1. A sealed lead-acid battery in which oxygen gas generated during charging of the battery is absorbed by a negative electrode, and a positive electrode plate and a negative electrode plate each having a thin glass paper made of fine glass fibers attached to both sides thereof and a low resistance plate. The electrode plate group consisting of the separator is stored in the battery case, and
Filling and arranging a porous powder obtained by granulating 10-40 millimicron silica fine powder using a binder, and impregnating and holding the above-mentioned granulated powder with a sufficient amount of sulfuric acid electrolyte necessary for discharge. A sealed lead-acid battery that is characterized by:
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63312181A JPH0654680B2 (en) | 1988-12-09 | 1988-12-09 | Sealed lead acid battery |
AU46088/89A AU623712B2 (en) | 1988-12-09 | 1989-12-08 | Sealed lead-acid battery |
DE68917283T DE68917283T2 (en) | 1988-12-09 | 1989-12-08 | Gas-tight lead-acid battery. |
US07/447,938 US5035966A (en) | 1988-12-09 | 1989-12-08 | Sealed lead-acid battery |
EP89122676A EP0377828B1 (en) | 1988-12-09 | 1989-12-08 | Sealed lead-acid battery |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63312181A JPH0654680B2 (en) | 1988-12-09 | 1988-12-09 | Sealed lead acid battery |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02158062A JPH02158062A (en) | 1990-06-18 |
JPH0654680B2 true JPH0654680B2 (en) | 1994-07-20 |
Family
ID=18026193
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63312181A Expired - Fee Related JPH0654680B2 (en) | 1988-12-09 | 1988-12-09 | Sealed lead acid battery |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0654680B2 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003067684A2 (en) | 2002-02-07 | 2003-08-14 | Kvg Technologies, Inc. | Lead acid battery with gelled electrolyte formed by filtration action of absorbent separators, electrolyte therefor, and absorbent separators therefor |
-
1988
- 1988-12-09 JP JP63312181A patent/JPH0654680B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JPH02158062A (en) | 1990-06-18 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
LAPS | Cancellation because of no payment of annual fees |