JPS58111277A - Sealed lead storage battery - Google Patents

Sealed lead storage battery

Info

Publication number
JPS58111277A
JPS58111277A JP56212609A JP21260981A JPS58111277A JP S58111277 A JPS58111277 A JP S58111277A JP 56212609 A JP56212609 A JP 56212609A JP 21260981 A JP21260981 A JP 21260981A JP S58111277 A JPS58111277 A JP S58111277A
Authority
JP
Japan
Prior art keywords
electrolyte
palladium
retainer
battery
supported
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
Application number
JP56212609A
Other languages
Japanese (ja)
Inventor
Takao Ogura
孝夫 小倉
Toshiyuki Matsumura
敏之 松村
Itsuro Takeda
竹田 逸郎
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.)
Resonac Corp
Original Assignee
Shin Kobe Electric Machinery 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 Shin Kobe Electric Machinery Co Ltd filed Critical Shin Kobe Electric Machinery Co Ltd
Priority to JP56212609A priority Critical patent/JPS58111277A/en
Publication of JPS58111277A publication Critical patent/JPS58111277A/en
Pending 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
    • H01M10/42Methods or arrangements for servicing or maintenance of secondary cells or secondary half-cells
    • H01M10/52Removing gases inside the secondary cell, e.g. by absorption
    • 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

Abstract

PURPOSE:To prevent any reduction in the amount of electrolyte by adding a pulverized catalyst powder, on which a noble metal is supported, into a retainer used for supporting the electrolyte, and directly converting oxygen and hydrogen generated during charging into water by catalysis. CONSTITUTION:A catalyst made of pulverized gamma-alumina or zeolite powder on which a noble metal such as palladium is supported, is added into a retainer 1 used for supporting electrolyte. After that, a lead storege battery is constituted by combining the retainer 1 with both a positive and a negative plate 2 and 3. Thus, by making palladium to the supported on the carrier, any generation of a local battery which might be caused due to the migration of palladium in the electrolyte is prevented, and the solubility of palladium in sulfuric acid is decreased by using gamma-alumina or zeolite as the carrier. As a result, oxygen and hydrogen generated during charging can be directly converted into water effectively by catalysis, and any reduction in the amount of the electrolyte can be prevented.

Description

【発明の詳細な説明】 本発明は密閉形船書電池中の電解液減少防止に関するも
のである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to prevention of electrolyte reduction in a sealed battery.

従来11m+5形船蓄電池に畠いて、負極板は充電中に
発生する酸素カスの吸収能力を有する。しかし、充電電
流か大会すぎるとこの酸素ミス吸収能力の限界を越える
こととtよる。そのため。
In the conventional 11m+5 type ship storage battery, the negative electrode plate has the ability to absorb oxygen scum generated during charging. However, if the charging current is too high, the limit of this oxygen miss absorption ability may be exceeded. Therefore.

密閉小形鉛蓄電池は急速充電に向いていtlいといわれ
ている。また、密閉小形鉛蓄電池は洩液しないことを特
徴としており、電池内の電解液量はおのずと限られてく
る。従って、急速充電により電解液の減少か起こると、
電解液の保持す を目的とした)テーナと称されるガラス繊維等の不織布
と極板との1着状態か悪くなり、内部抵抗の増加をまね
き容量か急速に低下することとなる。
Sealed small lead-acid batteries are suitable for rapid charging and are said to be TL. Furthermore, sealed small lead-acid batteries are characterized by no leakage, and the amount of electrolyte in the battery is naturally limited. Therefore, if the electrolyte decreases due to rapid charging,
The bond between the electrode plate and a non-woven fabric such as glass fiber called a retainer (for the purpose of retaining the electrolyte) deteriorates, leading to an increase in internal resistance and a rapid decrease in capacity.

本発明の目的は密閉形鉛蓄電池のリテーナ中に、パラジ
ウム等の貴金属を担持したr−アルミナ等の微粉末を添
加し、充電中化発生する酸素および水素を触媒作用で直
接水にすることkより、電解液量の減少を防ぐことであ
る。−次に本発明の実施例を説明する。
The purpose of the present invention is to add fine powder such as r-alumina supporting a noble metal such as palladium into the retainer of a sealed lead-acid battery, and to convert oxygen and hydrogen generated during charging directly into water through catalytic action. This is to prevent the amount of electrolyte from decreasing. - Next, embodiments of the present invention will be described.

電解液を繊維間の間隙より大きいr−アルミナあるいは
ゼオライトに通常の触媒調製法により、20A’以上の
パラジウムを担持する。この触媒を第1図のよう沁すテ
ーナ1間tC添加し。
Palladium of 20 A' or more is supported on r-alumina or zeolite, which is larger than the gap between the fibers, using an ordinary catalyst preparation method. This catalyst was added to the retainer for 1 tC as shown in Figure 1.

電池を組み立てる。パラジウムを担体に担持する理由は
パラジウムの電解液中ての移動番こより生ずる局部電池
の生成を防ぐためである。また。
Assemble the battery. The reason why palladium is supported on a carrier is to prevent the formation of local batteries due to movement of palladium in an electrolytic solution. Also.

担体であるr−アルミナおよびゼオライトは硫酸への溶
解度はわずかであり、溶出してもAg。
The supports, r-alumina and zeolite, have little solubility in sulfuric acid, and even if they are eluted, Ag remains.

CIt、 Naイオンは電池に影響を及ぼさない。CIt, Na ions have no effect on the battery.

なお2は正極板、3は負極板、4は触媒である。Note that 2 is a positive electrode plate, 3 is a negative electrode plate, and 4 is a catalyst.

第2図に従来の触媒を添加しない電池と添加した電流の
寿命試験量イクルに伴t1う電解液減少の状態を示す、
aIA電流電流カット定電圧入の場合、触媒添加化よる
効果はほとんどないか、3A電流カツト意電圧充電Bの
場合、その差は著しい。ここで、(115A電流カツト
で充電する場合ても、lI干の電解液減少かみられるか
Figure 2 shows the state of decrease in electrolyte with t1 of a battery without the addition of a conventional catalyst and the life test amount of the added current.
In the case of aIA current cut and constant voltage input, there is almost no effect of catalyst addition, and in the case of 3A current cut and voltage charging B, the difference is significant. Here, (even when charging with a 115A current cut, is there a significant decrease in electrolyte?

これは水の蒸発によるものである。This is due to water evaporation.

fEtdCは触媒添加時の8A電流カット定電圧充電池
は触媒添加時のa15A電流カット定電圧充電を示す。
fEtdC indicates 8A current cut constant voltage charging when catalyst is added, and a15A current cut constant voltage charging when catalyst is added.

第3図は3A電流カツト定電圧充電による寿命試験の容
量変化を示し、サイクル寿命試験の容量低下に対する触
媒添加効果を示す、当然のことなから、触媒添加した電
池とは電解液減少か少ないため容量低下および容量のバ
ラツキか少なくなる。嘴は従来の電池である。
Figure 3 shows the capacity change in the life test with constant voltage charging with a current cut of 3A, and shows the effect of catalyst addition on the capacity reduction in the cycle life test.As a matter of course, the battery with catalyst added has less electrolyte. Capacity decrease and capacity variation will be reduced. The beak is a conventional battery.

上述のよう番【本発明によれば、急速充電を行なった場
合ても急激な電池容量の劣下を防ぐことかてきる等工業
的価値甚だ大なるものである。
As mentioned above, the present invention has great industrial value, as it can prevent rapid deterioration of battery capacity even when rapid charging is performed.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は触媒を添加した極板群の概略断面図。 第2図は寿命試験時の電解液縛少量を示す曲線図、第3
図は3A電流カツト定電圧充電による寿命試験の容量変
化を示す曲線図である。 特許出願人 帛2図 、  :::I−一 /Y
FIG. 1 is a schematic cross-sectional view of a group of electrode plates to which a catalyst is added. Figure 2 is a curve diagram showing the amount of electrolyte bound during the life test;
The figure is a curve diagram showing a change in capacity in a life test using 3A current cut constant voltage charging. Patent applicant file 2, :::I-1/Y

Claims (1)

【特許請求の範囲】[Claims] 貴金属を担持した′触媒微粉末を電池に添加することを
特徴とする書Ws形船蓄電池。
A Ws-type ship storage battery characterized by adding catalyst fine powder supporting a precious metal to the battery.
JP56212609A 1981-12-24 1981-12-24 Sealed lead storage battery Pending JPS58111277A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56212609A JPS58111277A (en) 1981-12-24 1981-12-24 Sealed lead storage battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56212609A JPS58111277A (en) 1981-12-24 1981-12-24 Sealed lead storage battery

Publications (1)

Publication Number Publication Date
JPS58111277A true JPS58111277A (en) 1983-07-02

Family

ID=16625517

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56212609A Pending JPS58111277A (en) 1981-12-24 1981-12-24 Sealed lead storage battery

Country Status (1)

Country Link
JP (1) JPS58111277A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2526231A1 (en) * 1982-05-03 1983-11-04 Deutsche Automobilgesellsch METHOD AND DEVICE FOR RECOMBINING HYDROGEN AND OXYGEN DEGAGES IN AQUEOUS ELECTROLYTE ELECTRIC BATTERIES
FR2625370A1 (en) * 1987-12-25 1989-06-30 Pk Tekhnolo ELECTRICAL ACCUMULATOR

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2526231A1 (en) * 1982-05-03 1983-11-04 Deutsche Automobilgesellsch METHOD AND DEVICE FOR RECOMBINING HYDROGEN AND OXYGEN DEGAGES IN AQUEOUS ELECTROLYTE ELECTRIC BATTERIES
FR2625370A1 (en) * 1987-12-25 1989-06-30 Pk Tekhnolo ELECTRICAL ACCUMULATOR

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