JPS6319765A - Lead-acid battery - Google Patents

Lead-acid battery

Info

Publication number
JPS6319765A
JPS6319765A JP61164911A JP16491186A JPS6319765A JP S6319765 A JPS6319765 A JP S6319765A JP 61164911 A JP61164911 A JP 61164911A JP 16491186 A JP16491186 A JP 16491186A JP S6319765 A JPS6319765 A JP S6319765A
Authority
JP
Japan
Prior art keywords
powder
fine powder
lead
fine
liquid absorbing
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
JP61164911A
Other languages
Japanese (ja)
Inventor
Seiji Kamiharashi
征治 上原子
Hiroyuki Jinbo
裕行 神保
Keiko Naruse
成瀬 圭子
Sadao Fukuda
貞夫 福田
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.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial 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 Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP61164911A priority Critical patent/JPS6319765A/en
Publication of JPS6319765A publication Critical patent/JPS6319765A/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
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/62Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Battery Electrode And Active Subsutance (AREA)

Abstract

PURPOSE:To enhance the performance of a negative plate by adding fine liquid absorbing powder and fine conductive powder to a negative plate. CONSTITUTION:Specific fine liquid absorbing powder and fine conductive powder which covers conductivity decrease between particles and between active material and a grid caused by addition of the liquid absorbing powder are added to negative active material paste. The adding amount of the liquid absorbing powder is 0.01-3.0% of the total active material by weight, and that of the conductive powder is 0.01-3.0%. The liquid absorbing powder is zeolite whose sulfuric acid soluble ingredients are removed, and conductive powder is carbon. Particle size of the fine absorbing powder and fine conductive powder is 200mum or less.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は鉛蓄電池、とくにその負極板の特性向上のため
の添加剤に関するものである。
DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to lead-acid batteries, and particularly to additives for improving the characteristics of the negative electrode plate thereof.

従来の技術 従来の鉛蓄電池用負極板は、鉛あるいは鉛合金を鋳造あ
るいはエキスバンド加工などにより集電体格子を作製し
、この集電体に、主成分が酸化鉛よりなる活物質原料を
塗着、乾燥し、ついで化成して極板としていた。
Conventional technology In conventional negative electrode plates for lead-acid batteries, a current collector grid is produced by casting or expanding lead or lead alloy, and this current collector is coated with an active material whose main component is lead oxide. It was coated, dried, and then chemically converted into electrode plates.

ここでの活物質原料は酸化鉛を主体とする鉛粉と硫酸と
水を混合し練合したもので、機械的強度を改善するため
に耐酸性の合成樹脂繊維を添加したも′のである。
The active material raw material here is a mixture of lead powder, mainly lead oxide, sulfuric acid, and water, and acid-resistant synthetic resin fibers are added to improve mechanical strength.

またその他の添加剤として、硫酸バリウム、リグニンス
ルホン酸ナトリウムなどがあるのみである○ 発明が解決しようとする問題点 しかし、これらの添加剤のみでは近年発展の蓄しい密閉
形の鉛蓄電池、すなわち電解液量が少なく制限された電
池に要求される負極板の親水性および吸液性の向上には
不充分であった。本発明は、この負極板の特性向上を目
的としたものである。
Other additives include barium sulfate, sodium ligninsulfonate, etc. Problems to be Solved by the Invention However, these additives alone cannot be used for sealed lead-acid batteries, which have been developed in recent years, that is, electrolytic batteries. This was insufficient to improve the hydrophilicity and liquid absorbency of the negative electrode plate, which is required for batteries with limited liquid volume. The present invention aims to improve the characteristics of this negative electrode plate.

問題点を解決するための手段 本発明は負極板用の活物質ペーストに所定の吸液性の微
粉末の一定量と、この添加剤によって低下する粒子間お
よび活物質と格子界面の導電性を補なうため導電性の微
粉末の一定量を添加し、負極板の親水性、吸液性の向上
を図ったことを特徴としたものである。
Means for Solving the Problems The present invention incorporates a certain amount of predetermined liquid-absorbing fine powder into the active material paste for the negative electrode plate, and reduces the conductivity between particles and at the interface between the active material and the lattice, which is reduced by this additive. A certain amount of conductive fine powder is added to compensate for the negative electrode plate's hydrophilicity and liquid absorption.

作用 本発明による負極板は、電解液の吸液性が向上するため
、長期保存中に電解液中の水分が電槽壁を通して大気中
に拡散し減少して、電解液量が所定量より減少した場合
においても、吸液性に優れるためガラスマットから電解
液の供給を受は充分に保持出来る能力を有するものであ
る。
Function: Since the negative electrode plate according to the present invention has improved electrolyte absorbability, during long-term storage, water in the electrolyte diffuses into the atmosphere through the container wall and decreases, causing the amount of electrolyte to decrease below a predetermined amount. Even in such cases, the glass mat has the ability to sufficiently retain the electrolyte supplied from the glass mat due to its excellent liquid absorption properties.

このため、長期保存後の問題点の1つである負極板中の
電解液充填率の低下による容量の低下を抑制することが
出来る。
Therefore, it is possible to suppress a decrease in capacity due to a decrease in the electrolyte filling rate in the negative electrode plate, which is one of the problems after long-term storage.

実施例 以下、本発明の一実施例を説明する。従来のペースト処
方によって製作した負極板をA1および吸水性の微粉末
として平均粒径が約20μmのゼオライトを人の処方に
対して重量比で0.3係、および導電性の微粉末として
平均粒径が5μmのグラファイトカーボンを同じ<0.
25%添加して製作した負極板Bを用いて、電圧12v
1容量2.OAhの電池人およびBを製作した。
EXAMPLE An example of the present invention will be described below. The negative electrode plate produced by the conventional paste formulation was used as A1, water-absorbing fine powder, zeolite with an average particle size of about 20 μm at a weight ratio of 0.3 to the human recipe, and conductive fine powder with average particles. Graphite carbon with a diameter of 5 μm is the same <0.
Using negative electrode plate B made with 25% additive, the voltage was 12V.
1 capacity 2. I made OAh battery man and B.

この電池の製作条件は負極板の添加剤を除いてはすべて
同一条件で実施した。
This battery was manufactured under the same conditions except for the additive for the negative electrode plate.

製作した電池の初期容量および常温で2年間放置後の容
量の残存率と充電後の回復率の評価を行った。
The initial capacity of the produced battery, the remaining capacity after being left at room temperature for two years, and the recovery rate after charging were evaluated.

その結果を次表に示す。The results are shown in the table below.

(以下余白) なお、充放電条件は次の通りである。(Margin below) Note that the charging and discharging conditions are as follows.

(1)充電条件 定電圧充電;充電電流=80omA 設定電圧= 14.7 V 充電時間=6.o時間 (2)放電条件 放電電流=1.Q人 カプト電圧=10.5’V 発明の効果 表に示したように本発明を密閉形鉛蓄電池に適用するこ
とにより、長期保存時における自己放電量を抑制し容量
の残存率を高めるとともに充電後の回復率を大幅に向上
させることが出来るものである。
(1) Charging conditions Constant voltage charging; Charging current = 80 ohmA Set voltage = 14.7 V Charging time = 6. o time (2) discharge condition discharge current = 1. Q Capto voltage = 10.5'V As shown in the effect table of the invention, by applying the present invention to a sealed lead-acid battery, the amount of self-discharge during long-term storage is suppressed, the residual capacity rate is increased, and charging is possible. This can greatly improve the subsequent recovery rate.

Claims (4)

【特許請求の範囲】[Claims] (1)正極板、負極板、セパレータおよび電解液から構
成される鉛蓄電池であって、前記負極板に吸液性の微粉
末および導電性の微粉末を添加したことを特徴とする鉛
蓄電池。
(1) A lead-acid battery comprising a positive electrode plate, a negative electrode plate, a separator, and an electrolytic solution, characterized in that a liquid-absorbing fine powder and a conductive fine powder are added to the negative electrode plate.
(2)吸液性の微粉末の添加量が重量比で活物質総量の
0.01〜3.0%であり、導電性の微粉末の添加量が
0.01〜3.0%である特許請求の範囲第1項記載の
鉛蓄電池。
(2) The amount of liquid-absorbing fine powder added is 0.01 to 3.0% by weight of the total amount of active materials, and the amount of conductive fine powder added is 0.01 to 3.0%. A lead-acid battery according to claim 1.
(3)吸液性の微粉末が硫酸可溶性成分を除いたゼオラ
イトであり、導電性の微粉末がカーボンである特許請求
の範囲第1項記載の鉛蓄電池。
(3) The lead-acid battery according to claim 1, wherein the liquid-absorbing fine powder is zeolite from which sulfuric acid-soluble components have been removed, and the conductive fine powder is carbon.
(4)吸液性の微粉末の粒径が200μm以下であり、
導電性の微粉末の粒径が200μm以下である特許請求
の範囲第1項記載の鉛蓄電池。
(4) The particle size of the liquid-absorbing fine powder is 200 μm or less,
The lead-acid battery according to claim 1, wherein the conductive fine powder has a particle size of 200 μm or less.
JP61164911A 1986-07-14 1986-07-14 Lead-acid battery Pending JPS6319765A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61164911A JPS6319765A (en) 1986-07-14 1986-07-14 Lead-acid battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61164911A JPS6319765A (en) 1986-07-14 1986-07-14 Lead-acid battery

Publications (1)

Publication Number Publication Date
JPS6319765A true JPS6319765A (en) 1988-01-27

Family

ID=15802201

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61164911A Pending JPS6319765A (en) 1986-07-14 1986-07-14 Lead-acid battery

Country Status (1)

Country Link
JP (1) JPS6319765A (en)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58123658A (en) * 1982-01-19 1983-07-22 Matsushita Electric Ind Co Ltd Sealed lead storage battery
JPS5933760A (en) * 1982-08-18 1984-02-23 Yuasa Battery Co Ltd Electrode plate for lead-acid battery

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58123658A (en) * 1982-01-19 1983-07-22 Matsushita Electric Ind Co Ltd Sealed lead storage battery
JPS5933760A (en) * 1982-08-18 1984-02-23 Yuasa Battery Co Ltd Electrode plate for lead-acid battery

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