JPH02158063A - Sealed lead-storage battery - Google Patents
Sealed lead-storage batteryInfo
- Publication number
- JPH02158063A JPH02158063A JP63312182A JP31218288A JPH02158063A JP H02158063 A JPH02158063 A JP H02158063A JP 63312182 A JP63312182 A JP 63312182A JP 31218288 A JP31218288 A JP 31218288A JP H02158063 A JPH02158063 A JP H02158063A
- Authority
- JP
- Japan
- Prior art keywords
- plate group
- electrolyte
- battery
- electrode plate
- granules
- 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.)
- Granted
Links
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 14
- 239000011230 binding agent Substances 0.000 claims abstract description 4
- 239000003365 glass fiber Substances 0.000 claims abstract description 4
- 239000002253 acid Substances 0.000 claims description 8
- 239000000377 silicon dioxide Substances 0.000 claims description 6
- 239000000843 powder Substances 0.000 claims description 5
- 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
- 238000007599 discharging Methods 0.000 claims 1
- 239000008151 electrolyte solution Substances 0.000 claims 1
- 230000000717 retained effect Effects 0.000 claims 1
- 239000003792 electrolyte Substances 0.000 abstract description 13
- 239000008187 granular material Substances 0.000 abstract description 8
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract description 6
- 230000005484 gravity Effects 0.000 abstract description 4
- 238000003825 pressing Methods 0.000 abstract 1
- 239000000835 fiber Substances 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 239000011361 granulated particle Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 229910001128 Sn alloy Inorganic materials 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000011164 primary particle Substances 0.000 description 1
- 239000011163 secondary particle Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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
- H01M10/06—Lead-acid accumulators
- H01M10/08—Selection of materials as electrolytes
- H01M10/10—Immobilising of electrolyte
-
- 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
-
- 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
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Secondary Cells (AREA)
Abstract
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。[Detailed description of the invention] Industrial applications The present invention relates to improvements in sealed lead-acid batteries.
従来の技術とその課題
電池の充電中に発生ず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カラ
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、ポータプル機
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や
一方、ゲル式はリテーナ式より電池性能が劣るという欠
点があった。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 battery charging. The retainer type inserts a matte separator (glass separator) made of fine glass fiber between the positive and negative electrode plates, which holds the sulfuric acid electrolyte necessary for discharge and isolates the two electrodes. In recent years, it has become widely used as a backup power source for portable devices and computers. However, since the retainer type cannot hold a sufficient amount of electrolyte, it has the disadvantage that the discharge capacity is limited by the amount of electrolyte at low rate discharge, which is an obstacle to the spread of this type of sealed battery. On the other hand, the gel type had the disadvantage that its battery performance was 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
、漠れな放電性能を有する密閉式1g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セパレータと、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、限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 drawbacks of the conventional sealed lead-acid batteries mentioned above and provides a sealed 1g storage battery with poor discharge performance. A sufficient amount of sulfuric acid electrolyte necessary for discharge is filled around the separator and the electrode plate group, and is impregnated into porous powder made by granulating silica micropowder with a binder. be. The present invention will be explained 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、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
極未化成極板と十分に高い気孔率と表面積を有する徴紹
ガラスw&維(繊維の直径0.5〜1ミクロン)の抄紙
セパレータを用いて極板群を作製し、電槽に挿入した。Example Positive and negative electrode grids made of a Pb--Ca--Sn alloy were filled with normal positive and negative electrode pastes and aged to produce unformed electrode plates. Next, an electrode plate group was prepared using these unformed positive and negative electrode plates and a paper separator made of glass w/fiber (fiber diameter 0.5 to 1 micron) having sufficiently high porosity and surface area, and an electrode plate group was prepared using the unformed positive electrode and negative electrode plates and a paper separator made of glass w&fiber (fiber diameter: 0.5 to 1 micron) with sufficiently high porosity and surface area. inserted into the tank.
そこで、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%
加えた水で練合して粒径を100〜200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−次粒子が凝集して100〜200ミクロンの二次
粒子になっており、この造粒粒子の気孔率は90%以上
、また間隙に充填した状態での気孔率は約85%であっ
た。Therefore, we used fine silica powder with a particle size of 10 to 40 mm and 15% methyl methacrylate as a binder.
The mixture was kneaded with added water, granulated to a particle size of 100 to 200 microns, and dried, and then packed tightly between the container wall and the electrode plate group while applying vibration. The granulated material filled here is made up of secondary particles of 100 to 200 microns by agglomeration of fine primary particles of silica, and the porosity of these granulated particles is over 90%, and the porosity of the granulated particles is 90% or more, and the porosity of the granulated particles is 90% or more. The porosity was about 85%.
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Ji4.5^hの密閉式鉛蓄電池を
作製し、容置試験に供した。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
電池を作製して本発明品と性能の比較を行った。第1表
にその試験結果を示す。After filling the granules in this manner, a lid was attached and an exhaust valve was attached to produce a sealed lead-acid battery with a nominal capacity of Ji4.5^h, which was subjected to a storage test. For comparison, a conventional retainer type battery and a gel type battery were prepared using electrode plates from the same lot, and their performance was compared with the product of the present invention. Table 1 shows the test results.
第1表
この試@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1量れていた。Table 1 This test result shows that when comparing the retainer type and the gel type, the retainer type had a slightly higher electrolyte specific gravity, so the high rate discharge performance was 1 amount higher than the gel type.
方、本発明品はこれら従来の密閉′A鈴蓄電池に比べて
低率放電、高率放電とも10〜20%も性能が向上した
。これは極板群の周囲にシリカ造粒物を充填したことに
よってリテーナ式よりも多い電解液を保持でき、しかも
ゲル式よりも電解液比重を高くできたからである。なお
、ゲル式で電解液比重を高くするとゲルの性能が変わり
、電池性能はむしろ低下してしまう。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 compared to these conventional sealed A-bell storage batteries. This is because by filling the periphery of the electrode plate group with silica granules, more electrolyte can be held than in the retainer type, and the specific gravity of the electrolyte can be made higher than in the gel type. Note that if the specific gravity of the electrolyte is increased in a gel type battery, the performance of the gel will change, and the battery performance will actually deteriorate.
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
鉛蓄電池は電解液をtR細ガラス抄紙セパレータと極板
群周囲に配置したシリカ微粉体の造粒物に含浸、保持さ
せることによって、従来形の密閉式鉛蓄電池の性能を大
幅に向上でき、その工業的価値は大きい。Effects of the Invention As is clear from the above embodiments, the sealed lead-acid battery according to the present invention impregnates and retains an electrolyte in the silica fine powder granules placed around the tR fine glass paper separator and the electrode plate group. As a result, the performance of conventional sealed lead-acid batteries can be greatly improved, and its industrial value is great.
Claims (1)
る密閉式鉛蓄電池において、正極板と負極板および十分
に高い気孔率と表面積を有する微細ガラス繊維の抄紙セ
パレータとからなる極板群を強く圧迫して電槽内に収納
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、電池の充放電に必要な電解液
を上記抄紙セパレータと極板群周囲に配置した上記造粒
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. In a sealed lead-acid battery in which oxygen gas generated during battery charging is absorbed by the negative electrode, an electrode plate group consisting of a positive electrode plate, a negative electrode plate, and a fine glass fiber paper separator having a sufficiently high porosity and surface area is used. While strongly compressing and storing the battery in a battery case, porous powder made by granulating silica micropowder of 10 to 40 millimicrons with a binder is filled and arranged around the electrode plate group, and the battery is sealed. A sealed lead-acid battery characterized in that an electrolytic solution necessary for charging and discharging is impregnated and retained in the granulated powder arranged around the paper separator and the electrode plate group.
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63312182A JPH0693366B2 (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 |
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 |
DE68917283T DE68917283T2 (en) | 1988-12-09 | 1989-12-08 | Gas-tight lead-acid battery. |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63312182A JPH0693366B2 (en) | 1988-12-09 | 1988-12-09 | Sealed lead acid battery |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02158063A true JPH02158063A (en) | 1990-06-18 |
JPH0693366B2 JPH0693366B2 (en) | 1994-11-16 |
Family
ID=18026206
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63312182A Expired - Fee Related JPH0693366B2 (en) | 1988-12-09 | 1988-12-09 | Sealed lead acid battery |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0693366B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7682738B2 (en) | 2002-02-07 | 2010-03-23 | Kvg Technologies, Inc. | Lead acid battery with gelled electrolyte formed by filtration action of absorbent separators and method for producing it |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5778775A (en) * | 1980-10-31 | 1982-05-17 | Matsushita Electric Ind Co Ltd | Sealed lead battery |
JPS60133667A (en) * | 1983-12-22 | 1985-07-16 | Shin Kobe Electric Mach Co Ltd | Sealed lead-acid battery manufacturing method |
JPS61198573A (en) * | 1985-02-27 | 1986-09-02 | Shin Kobe Electric Mach Co Ltd | Enclosed lead storage battery |
-
1988
- 1988-12-09 JP JP63312182A patent/JPH0693366B2/en not_active Expired - Fee Related
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5778775A (en) * | 1980-10-31 | 1982-05-17 | Matsushita Electric Ind Co Ltd | Sealed lead battery |
JPS60133667A (en) * | 1983-12-22 | 1985-07-16 | Shin Kobe Electric Mach Co Ltd | Sealed lead-acid battery manufacturing method |
JPS61198573A (en) * | 1985-02-27 | 1986-09-02 | Shin Kobe Electric Mach Co Ltd | Enclosed lead storage battery |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7682738B2 (en) | 2002-02-07 | 2010-03-23 | Kvg Technologies, Inc. | Lead acid battery with gelled electrolyte formed by filtration action of absorbent separators and method for producing it |
Also Published As
Publication number | Publication date |
---|---|
JPH0693366B2 (en) | 1994-11-16 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
LAPS | Cancellation because of no payment of annual fees |