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JPH02158063A - Sealed lead-storage battery - Google Patents

Sealed lead-storage battery

Info

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
Application number
JP63312182A
Other languages
Japanese (ja)
Other versions
JPH0693366B2 (en
Inventor
Akio Tokunaga
徳永 昭夫
Toshiaki Hayashi
俊明 林
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 JP63312182A priority Critical patent/JPH0693366B2/en
Priority to AU46088/89A priority patent/AU623712B2/en
Priority to US07/447,938 priority patent/US5035966A/en
Priority to EP89122676A priority patent/EP0377828B1/en
Priority to DE68917283T priority patent/DE68917283T2/en
Publication of JPH02158063A publication Critical patent/JPH02158063A/en
Publication of JPH0693366B2 publication Critical patent/JPH0693366B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00Secondary cells; Manufacture thereof
    • H01M10/06Lead-acid accumulators
    • H01M10/08Selection of materials as electrolytes
    • H01M10/10Immobilising of electrolyte
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00Secondary cells; Manufacture thereof
    • H01M10/34Gastight accumulators
    • H01M10/342Gastight lead accumulators
    • 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
    • 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
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P70/00Climate change mitigation technologies in the production process for final industrial or consumer products
    • Y02P70/50Manufacturing 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

PURPOSE:To obtain a sealed lead-storage battery whose discharge performance is remarkably increased by impregnating and holding an electrolyte in a separator made of fine glass fibers and granules of fine silica particles filled around a plate group. CONSTITUTION:A plate group comprising a positive plate, a negative plate, and a separator having high porosity and large surface area, made of fine glass fibers is put in a container by applying pressure. Porous granules prepared with 10-40mum fine silica particles and a binder are filled around the plate group. The amount of sulfuric acid electrolyte necessary and enough for charge- discharge is impregnated and held in the separator and the granules. By tilling the granules around the plate group, larger amount of electrolyte than a retainer type battery is held and specific gravity of the electrolyte is heightened than a gelled type battery. Low rate and high rate discharge performance is increased.

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)

【特許請求の範囲】[Claims] 1、電池の充電中に発生する酸素ガスを負極で吸収させ
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.
JP63312182A 1988-12-09 1988-12-09 Sealed lead acid battery Expired - Fee Related JPH0693366B2 (en)

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)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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

Patent Citations (3)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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

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