JPH04118854A - Gel type lead storage battery - Google Patents
Gel type lead storage batteryInfo
- Publication number
- JPH04118854A JPH04118854A JP2238517A JP23851790A JPH04118854A JP H04118854 A JPH04118854 A JP H04118854A JP 2238517 A JP2238517 A JP 2238517A JP 23851790 A JP23851790 A JP 23851790A JP H04118854 A JPH04118854 A JP H04118854A
- Authority
- JP
- Japan
- Prior art keywords
- separator
- battery
- powder
- gel type
- mixing
- 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
Links
- 239000002253 acid Substances 0.000 claims abstract description 12
- 239000000843 powder Substances 0.000 claims abstract description 12
- 239000012209 synthetic fiber Substances 0.000 claims abstract description 5
- 229920002994 synthetic fiber Polymers 0.000 claims abstract description 5
- 239000000203 mixture Substances 0.000 claims abstract 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 10
- 239000000835 fiber Substances 0.000 abstract description 5
- 229920000728 polyester Polymers 0.000 abstract description 4
- 239000000377 silicon dioxide Substances 0.000 abstract description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 3
- 239000003463 adsorbent Substances 0.000 abstract description 2
- 239000011230 binding agent Substances 0.000 abstract description 2
- 239000008119 colloidal silica Substances 0.000 abstract description 2
- 239000000126 substance Substances 0.000 abstract 1
- 239000003792 electrolyte Substances 0.000 description 6
- 239000011521 glass Substances 0.000 description 5
- 230000006866 deterioration Effects 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 3
- 239000011149 active material Substances 0.000 description 3
- 238000009792 diffusion process Methods 0.000 description 3
- 238000007599 discharging Methods 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 239000008151 electrolyte solution Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000011245 gel electrolyte Substances 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011163 secondary particle Substances 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
Landscapes
- Cell Separators (AREA)
Abstract
Description
【発明の詳細な説明】 産業上の利用分野 本発明はゲル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 gel type lead acid batteries.
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Ha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
パレータが高価なために、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 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 Ha 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, the glass separator of the retainer type is expensive, which is an obstacle to the widespread use of this type of sealed battery.
一方、ゲル式はリテーナ式よりも安価であるが、高率放
電性能や寿命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, although the gel type is cheaper than the retainer type, it has the disadvantage that its high rate discharge performance and life performance are inferior to the liquid type and retainer type.
ゲル式電池では電解液がゲル化によって非流動化されて
いるため、電解液中の硫酸イオンの拡散速度が遅く、硫
酸イオンの拡散速度によって制限される高率放電容態が
劣っているものと考えられる。また、ゲル式電池では、
充放電を繰り返ずうちに、次第に水分(H2O)が失わ
れてゲル状電解液にひび割れを生じて、電解液が遊離し
、この遊離した電解液が下部に蓄積し、その結果、極板
下部が優先的に充放電され、極板下部の劣化が促進され
ることとなる。下部で活物質が劣化すると次に極板上部
で充放電反応が集中し、この部分での劣化が促進され電
池として寿命になるものと推定される。In gel batteries, the electrolyte is non-fluid due to gelation, so the diffusion rate of sulfate ions in the electrolyte is slow, and it is thought that the high rate discharge capacity, which is limited by the diffusion rate of sulfate ions, is inferior. It will be done. In addition, with gel batteries,
As charging and discharging are repeated, water (H2O) is gradually lost and cracks occur in the gel electrolyte, which liberates the electrolyte. This liberated electrolyte accumulates at the bottom, and as a result, the electrode plate The lower part is preferentially charged and discharged, and the deterioration of the lower part of the electrode plate is accelerated. It is presumed that once the active material deteriorates in the lower part, the charging and discharging reactions will then concentrate in the upper part of the electrode plate, accelerating the deterioration in this part and ending the life of the battery.
課題を解決するための手段
本発明は、上述した従来のゲル式鉛電池の問題点を解決
するもので、その要旨とするところは、ゲル式鉛蓄電池
のセパレータとして従来より使用されれてきた合成樹脂
またはバルブセパレータなどに代わり、耐酸性無機粉体
と合成繊維とを混抄して製作したセパレータ(以下混抄
セパレータと称する)を使用することで、セパレータの
電気抵抗を下げることで高率放電性能を改善し、同時に
充放電反応を均一化することで電池寿命も改善すること
にある。Means for Solving the Problems The present invention solves the above-mentioned problems of conventional gel-type lead-acid batteries. By using separators made by mixing acid-resistant inorganic powder and synthetic fibers (hereinafter referred to as mixed paper separators) instead of resin or valve separators, we can lower the electrical resistance of the separators and improve high-rate discharge performance. The aim is to improve battery life by simultaneously making the charging and discharging reactions more uniform.
実施例 以下本発明を実施例にて詳述する。Example The present invention will be explained in detail below with reference to Examples.
まず、本発明電池のセパレータとして使用した混抄セパ
レータについて説明する。長さ約101゜繊維径0.5
デニールのポリエステル繊維30wt%およびシリカ粉
末70wt%を水に分散させ、ついでこの中に吸着剤お
よび少量のバインダーを入れてポリエステル繊維に粉体
を吸着させ、抄造、乾燥し厚さ約1.2mmの混抄セパ
レータを作製した。ここで用いたシリカ粉末は2次粒子
あるいは3次粒子が20μm以下の通常用いられている
ものを用いた。First, the mixed paper separator used as the separator of the battery of the present invention will be explained. Length approx. 101° Fiber diameter 0.5
Disperse 30wt% of denier polyester fiber and 70wt% of silica powder in water, then add an adsorbent and a small amount of binder to make the powder adsorb to the polyester fiber, form a paper, and dry it to a thickness of about 1.2mm. A mixed paper separator was produced. The silica powder used here was a commonly used silica powder having secondary particles or tertiary particles of 20 μm or less.
この方法により作製した混抄セパレータを用いて、コロ
イダルシリカ7%含む希硫酸を注液した電解液比重1.
30のゲル式電池Aを作製した。比較のために、同じ厚
さ(1,211n厚)の平パルプセパレータを使用した
ゲル式電池Bを作製した。Using the mixed paper separator produced by this method, dilute sulfuric acid containing 7% colloidal silica was injected into an electrolytic solution with a specific gravity of 1.
Thirty gel type batteries A were produced. For comparison, a gel type battery B was produced using a flat pulp separator of the same thickness (1,211 nm thick).
ここで作製した電池の公称容量は5hR容量で28^h
の自動車用密閉式鉛蓄電池である。電池A、 Bは初期
容量試験後、自動車電池用JIS寿命試験に入れ放電容
量が規格値の70%となったサイクル数をもって寿命と
した。その結果を第1表に示す。The nominal capacity of the battery produced here is 5hR capacity and 28^h
This is a sealed lead-acid battery for automobiles. After the initial capacity test, batteries A and B were subjected to a JIS life test for automobile batteries, and the life span was defined as the number of cycles at which the discharge capacity reached 70% of the standard value. The results are shown in Table 1.
第1表
第1表の結果より、セパレータとして混抄マットを使用
した電池Aは、従来のバルブセパレータを用いた電池B
に比べて5hR容量はほとんど変わらないものの、ハイ
レート容量が優れているのみならず、特にJIS 寿命
が200〜から400〜と2倍になった。Table 1 From the results in Table 1, battery A using a mixed paper mat as a separator is different from battery B using a conventional valve separator.
Although the 5hR capacity is almost the same as that of the previous model, not only is the high rate capacity superior, but the JIS life span has doubled from 200 to 400.
この原因としては、電解液はゲル状となっているので硫
酸イオンの拡散速度は変わらないものの、バルブセパレ
ータ等に比べると今回使用した混抄マットは電気抵抗が
小さく、ハイレート放電時の電圧降下が小さくなり、そ
の結果ハイレート容量が優れていたものと思われる。ま
た、ゲル式鉛蓄電池を充放電サイクルしたときに生成す
る遊離液も、混抄マットの吸液性がバルブセパレータ等
に比べて優れていて、遊離液が混抄マットに吸収される
ため、充放電反応が局部的に集中することなく均一に行
われることになり、活物質の劣化もおだやかでこのよう
な長寿命になったと考えられる。The reason for this is that although the electrolyte is in a gel state, the diffusion rate of sulfate ions remains the same, but compared to valve separators, the mixed mat used this time has a lower electrical resistance and a lower voltage drop during high-rate discharge. As a result, it seems that the high-rate capacity was excellent. In addition, the free liquid generated when a gel type lead-acid battery is charged and discharged is also absorbed by the mixed mat because the absorbency of the mixed paper mat is superior to that of valve separators, etc. This is thought to be the reason for the long lifespan due to the fact that the deterioration of the active material is gradual, as the deterioration of the active material is performed uniformly without being locally concentrated.
なお、混抄マットはリテーナ式鉛蓄電池に使用されるガ
ラスセパレータに比べて安価なもので、コスト面でもガ
ラスセパレータより優れている。Note that the mixed mat is cheaper than the glass separator used in caged lead-acid batteries, and is superior to the glass separator in terms of cost.
発明の効果
以上詳述したように本発明によるゲル式鉛蓄電池は、耐
酸性無機粉体と合成繊維とを混抄して製作したセパレー
タを用いることによって、高率放電性能および電池寿命
を改善することができ、かつガラスセパレータに比べて
コネト面でも安価であり、その工業的価値は大きい。Effects of the Invention As detailed above, the gel type lead-acid battery according to the present invention improves high rate discharge performance and battery life by using a separator made by mixing acid-resistant inorganic powder and synthetic fiber. It is also cheaper in terms of connectivity than glass separators, and its industrial value is great.
Claims (1)
レータを使用したゲル式鉛蓄電池。1. A gel type lead-acid battery that uses a separator made from a mixture of acid-resistant inorganic powder and synthetic fiber.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2238517A JPH04118854A (en) | 1990-09-07 | 1990-09-07 | Gel type lead storage battery |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2238517A JPH04118854A (en) | 1990-09-07 | 1990-09-07 | Gel type lead storage battery |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04118854A true JPH04118854A (en) | 1992-04-20 |
Family
ID=17031433
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2238517A Pending JPH04118854A (en) | 1990-09-07 | 1990-09-07 | Gel type lead storage battery |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04118854A (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 |
-
1990
- 1990-09-07 JP JP2238517A patent/JPH04118854A/en active Pending
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 |
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