JPH01102860A - Sealed lead-acid battery - Google Patents
Sealed lead-acid batteryInfo
- Publication number
- JPH01102860A JPH01102860A JP62260267A JP26026787A JPH01102860A JP H01102860 A JPH01102860 A JP H01102860A JP 62260267 A JP62260267 A JP 62260267A JP 26026787 A JP26026787 A JP 26026787A JP H01102860 A JPH01102860 A JP H01102860A
- Authority
- JP
- Japan
- Prior art keywords
- electrode plate
- electrolyte
- sio2
- neg
- gel
- 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 title claims description 17
- 239000003792 electrolyte Substances 0.000 claims abstract description 20
- 239000003365 glass fiber Substances 0.000 claims abstract description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 238000005215 recombination Methods 0.000 claims 1
- 230000006798 recombination Effects 0.000 claims 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 17
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract description 12
- 239000011148 porous material Substances 0.000 abstract description 8
- 239000002245 particle Substances 0.000 abstract description 2
- 229910052681 coesite Inorganic materials 0.000 abstract 5
- 229910052906 cristobalite Inorganic materials 0.000 abstract 5
- 239000000377 silicon dioxide Substances 0.000 abstract 5
- 235000012239 silicon dioxide Nutrition 0.000 abstract 5
- 229910052682 stishovite Inorganic materials 0.000 abstract 5
- 229910052905 tridymite Inorganic materials 0.000 abstract 5
- 239000000126 substance Substances 0.000 abstract 4
- 239000013543 active substance Substances 0.000 abstract 2
- 238000007599 discharging Methods 0.000 abstract 2
- 238000010276 construction Methods 0.000 abstract 1
- 239000006185 dispersion Substances 0.000 abstract 1
- 239000000706 filtrate Substances 0.000 abstract 1
- 150000002500 ions Chemical class 0.000 abstract 1
- 239000001117 sulphuric acid Substances 0.000 abstract 1
- 235000011149 sulphuric acid Nutrition 0.000 abstract 1
- 239000011245 gel electrolyte Substances 0.000 description 7
- 239000011149 active material Substances 0.000 description 6
- 230000005484 gravity Effects 0.000 description 6
- 230000007423 decrease Effects 0.000 description 4
- 239000000499 gel Substances 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 238000009792 diffusion process Methods 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- 239000008119 colloidal silica Substances 0.000 description 2
- 239000008151 electrolyte solution Substances 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- 238000005411 Van der Waals force Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000007773 negative electrode material Substances 0.000 description 1
- 238000002161 passivation Methods 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-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
- H01M10/12—Construction or manufacture
-
- 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
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明は密閉鉛蓄電池、特にクラッド式正極板を備えた
密閉鉛電池の改良に関するものである。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to improvements in sealed lead-acid batteries, particularly sealed lead-acid batteries with clad positive plates.
従来の技術とその問題点
密閉鉛蓄電池は、従来から正極板にペースト式横板を使
用したものとクラッド式極板を使用したものとがある。Conventional technology and its problems Sealed lead-acid batteries have conventionally been classified into two types: those using a paste-type horizontal plate as the positive electrode plate and those using a clad-type electrode plate.
前者の特徴は放電性能が優れていることであり、後者は
寿命性能に特徴があるがこれらの特徴は液式(開放形)
鉛蓄電池においても見られる特徴である。従来のクラッ
ド式正極板を備えた密閉鉛蓄電池においては、正負極板
間に合成樹脂製のセパレータや多孔板が配置され、コロ
イダルシリカ(SiO2)などでゲル状にした希硫酸よ
りなる電解液が注入されている。クラッド式極板はべ一
皮ト式に比し活物質の利用率が悪くその上、ゲル状電解
液になると、硫酸分がゲルに包み込まれて、しっかり固
定されているために拡散しがたく放電容量はかなり低下
する。更に負極板に関しても活物質の細孔内にゲル状電
解液が入り込み、そのS:02のために電解液の拡散や
移動が悪くなって放電性能が低下するという欠点があっ
た。このようにゲル状電解液を用いたクラッド式密閉鉛
蓄電池にあってはクラッド式極板構造にもとづく放電性
能の低下と、ゲル状電解液自体に起因する放電性能の低
下とが1なって、開放形鉛蓄電池に比しかなり放電性能
が劣ることが避けられなかった。The former is characterized by excellent discharge performance, and the latter is characterized by long life performance, but these characteristics are different from liquid type (open type).
This is a feature also seen in lead-acid batteries. In conventional sealed lead-acid batteries with clad positive electrode plates, a synthetic resin separator or perforated plate is placed between the positive and negative electrode plates, and an electrolyte made of dilute sulfuric acid gelled with colloidal silica (SiO2) is used. Injected. Clad type electrode plates have a lower utilization rate of active material than single-skin type electrode plates, and in addition, when the electrolyte becomes a gel, the sulfuric acid is wrapped in gel and is firmly fixed, making it difficult to diffuse. Discharge capacity decreases considerably. Furthermore, regarding the negative electrode plate, there was a drawback that the gel electrolyte entered the pores of the active material, and the S:02 of the electrolyte deteriorated the diffusion and movement of the electrolyte, resulting in a decrease in discharge performance. In this way, in a clad sealed lead-acid battery using a gel electrolyte, there is a decrease in discharge performance due to the clad plate structure and a decrease in discharge performance due to the gel electrolyte itself. It was inevitable that the discharge performance would be considerably inferior to that of open lead-acid batteries.
問題点を解決するための手段
本発明はゲル電解液を使用したクラッド式密閉鉛蓄電池
の放電性能の向上を図るため、高濃度の硫酸電解液を用
いて拡散のおくれをカバーするとともに、正・負極板内
部の活物1[には5IO2ffiの少ない電解液が存在
するよう極板表面にSiO2のろ過作用のある多孔体を
配置することに特徴がある。Means for Solving the Problems The present invention aims to improve the discharge performance of a clad-type sealed lead-acid battery using a gel electrolyte, by using a highly concentrated sulfuric acid electrolyte to cover the diffusion delay, and to improve the positive and A feature is that a porous body having a filtering effect of SiO2 is arranged on the surface of the electrode plate so that an electrolytic solution containing less 5IO2ffi exists in the active material 1 inside the negative electrode plate.
実施例
従来より鉛蓄電池は電解液である希硫酸自体が活物質で
あるためその濃度を高くするほどlLi!容量は増加す
ることが知られている。しかし液式(17tt放形)l
!池の場合電解液比重をあまりに高くするとl!良や自
己fi電が増加し、また負極の不働態化が促進されるの
で約1.30 (20℃)を越える比重はほとんど実
用されていない。密部形においては、電解液量が制限さ
れるために液式よりも^比重電解液が使用可能となる。Example Conventionally, in lead-acid batteries, the electrolytic solution, dilute sulfuric acid itself, is the active material, so the higher its concentration, the more lLi! It is known that capacity increases. However, liquid type (17tt release type)
! In the case of a pond, if the specific gravity of the electrolyte is too high, l! A specific gravity exceeding about 1.30 (at 20° C.) is rarely put into practical use because it increases self-fi charge and promotes passivation of the negative electrode. In the closed type, the amount of electrolyte is limited, so it is possible to use a specific gravity electrolyte rather than in the liquid type.
特にコロイダルシリカや水ガラスなどを添加してゲル化
した1illll!I電解液においては、SiO2の三
次元網目構造の骨格にファンデルワールス力によって保
持されている硫酸イオンは拡散しにくいために従来と同
程度の比重では充分な容量が取り出せない。ゲル電解液
の場合の硫酸比重は1.30 (20℃)以上、1.
40(20℃)以下の範囲で従来の液式電池(比重1.
25〜1.30 )と同程度の放電性能が(りられるこ
とがわかった。In particular, 1illll is gelled by adding colloidal silica and water glass! In the I electrolyte, the sulfate ions held by the van der Waals force in the framework of the three-dimensional network structure of SiO2 are difficult to diffuse, so a sufficient capacity cannot be obtained with a specific gravity similar to that of conventional electrolytes. In the case of gel electrolyte, the sulfuric acid specific gravity is 1.30 (20°C) or more, 1.
Conventional liquid type batteries (specific gravity 1.
25 to 1.30).
次にゲル式密閉鉛蓄電池の放電性能を向上させる手段は
、正・負極板活物質細孔内のSiO2′fA度を低くし
て、出来るだけ硫酸の拡散や移動を容易にすることであ
る。前述したように5iOzは三次元骨格を形成してゲ
ル化するので、S+02ffiの多いほどそのゲルは強
固なつまり硫酸イオンが移動しにくくなる。本発明はこ
の欠点を除去するため、負極板表面に微細ガラス繊維を
主体とする多孔体を密接して配置し、ゲル状、電解液が
負極活物質の細孔内に侵入するのを阻止する構成をとっ
ている。Next, a means of improving the discharge performance of a gel-type sealed lead acid battery is to lower the SiO2'fA degree in the pores of the active material of the positive and negative electrode plates to facilitate the diffusion and movement of sulfuric acid as much as possible. As mentioned above, 5iOz forms a three-dimensional skeleton and gels, so the more S+02ffi there is, the stronger the gel becomes, that is, the harder it is for sulfate ions to move. In order to eliminate this drawback, the present invention disposes a porous material mainly composed of fine glass fibers closely on the surface of the negative electrode plate to prevent gel-like electrolyte from entering the pores of the negative electrode active material. It is structured.
この場合多孔体はゲル状電解液が負極板と直接接触する
のを防ぐとともに、多孔体の微細な細孔がSiO2粒子
をろ化する作用を果す。これにより負極板は実質上Si
O2がほとんど存在しない電解液中で放電することが可
能になる。なお、クラッド式正極板については、本来ガ
ラス繊維や合成樹脂繊維で作られたチューブで活物質表
面が包囲された構造であるからそのチューブが負極板に
当接した多孔体と同様な効果を有するので、特に対策は
必要ではない。In this case, the porous body prevents the gel electrolyte from coming into direct contact with the negative electrode plate, and the fine pores of the porous body serve to filter the SiO2 particles. As a result, the negative electrode plate is made of substantially Si.
It becomes possible to discharge in an electrolyte in which almost no O2 is present. In addition, since the clad type positive electrode plate originally has a structure in which the surface of the active material is surrounded by a tube made of glass fiber or synthetic resin fiber, the tube has the same effect as a porous body in contact with the negative electrode plate. Therefore, no special measures are required.
発明の効果
本発明による密閉鉛蓄電池は、ゲル電解液をもつクラッ
ド式鉛蓄電池の欠点である放電性能の悪さを改善し、は
ぼ液式(開放形)のクラッド式と同等の性能レベルにま
で到達できた。これによりクラッド式極板の特徴である
充放電サイクル寿命性能に優れた高性能密閉鉛蓄電池が
開発でき、従来の密閉鉛蓄電池では対応できなかった、
フォークリフト用や電力貯蔵用などの分野にも使用可能
である。Effects of the Invention The sealed lead-acid battery according to the present invention improves the poor discharge performance, which is a drawback of clad lead-acid batteries with gel electrolyte, and achieves a performance level equivalent to that of a clad type (open type) type. I was able to reach it. As a result, we were able to develop a high-performance sealed lead-acid battery with excellent charge-discharge cycle life performance, which is a characteristic of clad plates, which was not possible with conventional sealed lead-acid batteries.
It can also be used in fields such as forklifts and power storage.
Claims (1)
繊維を主体とする多孔体などとからなる極板群で、Si
O_2によりゲル化して実質上流動する電解液を持たな
い、酸素再結合方式による密閉鉛電池であつて、前記正
極板はクラッド式構造でありかつ負極板表面には前記ガ
ラス繊維を主体とする多孔体が密接されており、正およ
び負極板内部の電解液中のSiO_2濃度を正・負極板
間に存在する電解液中のそれよりも低くした密閉鉛蓄電
池。1. An electrode plate group consisting of a positive electrode plate, a negative electrode plate, and a porous body mainly composed of glass fibers interposed between these electrode plates.
It is a sealed lead-acid battery based on the oxygen recombination method, which is gelled by O_2 and does not have an electrolyte that flows substantially, and the positive electrode plate has a clad structure and the negative electrode plate has porous holes mainly made of the glass fibers on the surface of the negative electrode plate. A sealed lead-acid battery in which the electrolyte inside the positive and negative plates has a lower SiO_2 concentration than the electrolyte between the positive and negative plates.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62260267A JPH01102860A (en) | 1987-10-15 | 1987-10-15 | Sealed lead-acid battery |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62260267A JPH01102860A (en) | 1987-10-15 | 1987-10-15 | Sealed lead-acid battery |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01102860A true JPH01102860A (en) | 1989-04-20 |
Family
ID=17345679
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62260267A Pending JPH01102860A (en) | 1987-10-15 | 1987-10-15 | Sealed lead-acid battery |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01102860A (en) |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5835877A (en) * | 1981-08-26 | 1983-03-02 | Yuasa Battery Co Ltd | Closed type lead battery and its production method |
JPS603871A (en) * | 1983-06-22 | 1985-01-10 | Japan Storage Battery Co Ltd | Lead-acid battery |
-
1987
- 1987-10-15 JP JP62260267A patent/JPH01102860A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5835877A (en) * | 1981-08-26 | 1983-03-02 | Yuasa Battery Co Ltd | Closed type lead battery and its production method |
JPS603871A (en) * | 1983-06-22 | 1985-01-10 | Japan Storage Battery Co Ltd | Lead-acid battery |
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