JPS609062A - Manufacture of substrate for lead storage battery - Google Patents

Manufacture of substrate for lead storage battery

Info

Publication number
JPS609062A
JPS609062A JP58116509A JP11650983A JPS609062A JP S609062 A JPS609062 A JP S609062A JP 58116509 A JP58116509 A JP 58116509A JP 11650983 A JP11650983 A JP 11650983A JP S609062 A JPS609062 A JP S609062A
Authority
JP
Japan
Prior art keywords
strength
substrate
heat treatment
lead alloy
case
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
JP58116509A
Other languages
Japanese (ja)
Inventor
Atsushi Furukawa
淳 古川
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.)
Furukawa Battery Co Ltd
Original Assignee
Furukawa 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 Furukawa Battery Co Ltd filed Critical Furukawa Battery Co Ltd
Priority to JP58116509A priority Critical patent/JPS609062A/en
Publication of JPS609062A publication Critical patent/JPS609062A/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
    • H01M4/64Carriers or collectors
    • H01M4/82Multi-step processes for manufacturing carriers for lead-acid accumulators
    • H01M4/84Multi-step processes for manufacturing carriers for lead-acid accumulators involving casting
    • 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
    • H01M4/64Carriers or collectors
    • H01M4/66Selection of materials
    • H01M4/68Selection of materials for use in lead-acid accumulators
    • H01M4/685Lead alloys
    • 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)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Cell Electrode Carriers And Collectors (AREA)

Abstract

PURPOSE:To increase mechanical strength of a substrate by performing heat treatment of a lead alloy rolled plate containing a specific amount of Sb and As respectively at a specific temperature and for a specific time followed by quenching at a specific temperature in water. CONSTITUTION:Before and after a lead alloy rolled plate consisting of Sb manufactured by continuous casting rolling 2.1-4.5m/o, As 0.15-0.25m/o, the rest Pb is mechanically processed by stamping or expanding, the heat treatment is performed at 230-240 deg.C for 5-20min followed by quenching at 0-40 deg.C in water. In the case of an amount of addition under 2.1m/o, an effect of improving strength is little, while in case of exceeding 4.5m/o, self-discharge increases thus shortening a life of a battery. Further, when As is added, a crystal grain becomes fine while increasing strength. When the temperature of heat treatment is under 230 deg.C, the strength increases but endurance of 7.5kgfmm.<-2> can not be reached, while in case 240 deg.C is exceeded, it approaches to the melting point of a lead alloy thus making it unable to be heated.

Description

【発明の詳細な説明】 本発明は鉛蓄電池用基板の製造方法の改良に関するもの
である。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an improvement in a method for manufacturing a lead-acid battery substrate.

従来連続鋳造圧延法によシ得た鉛合金圧延板は連続操業
によるため作業性が極めてよく大量に生産することが出
来うるも、機械的強度に劣シ蓄電池用基板として充放電
サイクルを繰返すと伸びを生じ容易に短絡をおこし蓄電
池としての寿命を早めるものであった。
Lead alloy rolled sheets obtained by the conventional continuous casting and rolling method have excellent workability and can be produced in large quantities due to continuous operation, but they have poor mechanical strength and cannot be used as substrates for storage batteries after repeated charging and discharging cycles. This causes elongation and easily causes short circuits, shortening the lifespan of the storage battery.

従ってかかる基板の機械的強度を増大せしめることが強
く要望されているが、何等の改良方法が行なわれていな
いものであった。
Therefore, there is a strong demand for increasing the mechanical strength of such substrates, but no improvement method has been developed.

なお連続鋳造圧延による鉛合金基板をそのまま放置する
も時効硬化による強化はえられないものであった。
Note that even if the lead alloy substrate formed by continuous casting and rolling was left as is, it could not be strengthened by age hardening.

本発明はかかる現状に鑑み鋭意研死を行なった結果優れ
た機械的強度を有する蓄電池用基板を製造する方法を開
発したものである。即ち本発明方法は連続鋳造圧延にょ
シ製造したsp 2.1〜4.5 m10 、 As 
O,15〜0.25 m10 、残部pbよシなる鉛合
金圧延板を打抜きちるいはエキス・ぐンド等の機械加工
をする前あるいは後に2300〜240℃にて5〜20
分間熱処理した後、o。
In view of the current situation, the present invention is the result of extensive research and development of a method for manufacturing a storage battery substrate having excellent mechanical strength. That is, the method of the present invention uses continuous casting and rolling process to produce sp 2.1 to 4.5 m10, As
O, 15 to 0.25 m10, the balance being PB, before or after punching or machining such as extract/gun at 2300 to 240°C for 5 to 20 minutes.
After heat treatment for minutes, o.

〜40℃の水中にて急冷せしめたことを特徴とするもの
である。
It is characterized by being rapidly cooled in water at ~40°C.

本発明方法において合金組成として5bt−添加するこ
とによ、6 pb金合金強度を増大せしめるものである
がその添加蓋を2.1 m10未満では強度を向上せし
める効果が薄< 、4−5 rrv’oを超えた場合に
は自己放電が多くなシミ池の寿命が早くなる。XAsを
添加することによシ結晶粒を細かくして上^己同様強度
を増大せしめるものであるか、0.15 m10未満で
は結晶粒を粗大化して耐腐食性が著しく劣るものである
。又0.25 rrV’。
In the method of the present invention, the strength of the 6 pb gold alloy is increased by adding 5 bt to the alloy composition, but if the addition amount is less than 2.1 m10, the effect of improving the strength is weak. If it exceeds 'o', the life of the stain pond will be shortened due to the large amount of self-discharge. By adding XAs, the crystal grains are made finer and the strength is increased as in the above example, or if it is less than 0.15 m10, the crystal grains are coarsened and the corrosion resistance is significantly inferior. Also 0.25 rrV'.

を超えた場合には強度が低下する傾向がある。If it exceeds this, the strength tends to decrease.

又本発明方法は上記の合金に熱処理と急冷を行なうこと
によシ蓄電池用基板として使用しうる機械的強度即し7
.51史f問−2以上の耐力をうろことが出来るもので
ある。
In addition, the method of the present invention heat-treats and rapidly cools the above-mentioned alloy to improve its mechanical strength, which can be used as a storage battery substrate.
.. 51 History Questions - It is possible to have a proof strength of 2 or more.

而して熱処理温度を230°〜240℃の範囲に限定し
たが230℃未イMでは強度は向上するも7.5に9f
mm の耐力に達することが出来ず又240℃を超える
と鉛合金の融点に近くなシ加熱することが出来ない。
Therefore, the heat treatment temperature was limited to a range of 230° to 240°C, but if the temperature was lower than 230°C, the strength would improve, but the strength would be 7.5 to 9f.
It is not possible to reach a yield strength of 1 mm, and if the temperature exceeds 240°C, it cannot be heated to a temperature close to the melting point of the lead alloy.

なお熱処理時間を5〜20分間に限定したが5分未満で
はその効果をうろことが出来ず、20分を超えると結晶
粒が大きくなり粗大化して耐腐食性を低下せしめるもの
である。
Note that although the heat treatment time was limited to 5 to 20 minutes, if it is less than 5 minutes, the effect cannot be achieved, and if it is more than 20 minutes, the crystal grains become large and coarse, resulting in a decrease in corrosion resistance.

又急冷源[を0°〜40℃に限定した理由は、40℃を
超えた場合には急冷の効果が薄く基板を硬化せしめるこ
とが出来ないためである。次に本発明方法の実施例につ
いて説明する。
The reason why the quenching source is limited to 0° to 40°C is that if the temperature exceeds 40°C, the quenching effect is weak and the substrate cannot be hardened. Next, examples of the method of the present invention will be described.

実施例(1)〜(2) 2.4 m7’o Sb −0,i 5 m7’o A
s −Pl+の組成からなる連続鋳造圧延材を210℃
(比較例(1))、220℃(比較例(2))、230
℃(実施例(1))、240℃(実施例(2) ) 、
及び247℃(比較例(3))において10分間熱処理
を行なった後10℃の水中にて急冷して本発明基板及び
比較例基板をえた。
Examples (1) to (2) 2.4 m7'o Sb -0,i5 m7'o A
Continuously cast and rolled material with a composition of s -Pl+ was heated at 210°C.
(Comparative example (1)), 220°C (Comparative example (2)), 230
°C (Example (1)), 240 °C (Example (2)),
After heat treatment at 247° C. (Comparative Example (3)) for 10 minutes, the substrates were rapidly cooled in water at 10° C. to obtain a substrate of the present invention and a comparative example substrate.

ルrくして得た基板について機械的強度として耐力を測
定した結果は第1図に示す通りである。
The results of measuring the yield strength as mechanical strength of the substrate obtained in this manner are shown in FIG.

第1図よシ明らかの如く本発明基板は耐力が7 、5 
kyfvun 以上の値を示し十分に 1池川基板とし
て使用することが出来た。これに対し比J紋例基板7.
5kpf五m−2に達せず蓄電池用基板として使用する
ことが出来なかった。
As is clear from Fig. 1, the yield strength of the substrate of the present invention is 7,5.
It showed a value higher than kyfvun and was able to be used as a 1-Ikegawa substrate. On the other hand, the comparison board 7.
It could not reach 5kpf 5m-2 and could not be used as a storage battery substrate.

なお上記圧延材を熱処理しない場合には耐力は著しく低
く僅に2.0に9fnrm−2であった。又比較例(3
)の如く高温にて熱処理を行なった場合には圧延材が溶
融のおそれがあった。
In addition, when the above-mentioned rolled material was not heat-treated, the yield strength was extremely low and was only 2.0 to 9 fnrm-2. Also, comparative example (3
), there was a risk that the rolled material would melt if the heat treatment was performed at a high temperature.

実施例(3)〜(4) 実施例(1)における圧延材を230℃において10分
間熱処理を行なった後、10℃(実施例(3))、30
 ’C(実施例(4))、50℃(比較例(4))及び
80℃(比較例(5))の水中に投入して急冷せしめて
本発明基板及び比較例基板をえた。
Examples (3) to (4) The rolled material in Example (1) was heat treated at 230°C for 10 minutes, and then heated at 10°C (Example (3)) and 30°C.
'C (Example (4)), 50°C (Comparative Example (4)), and 80°C (Comparative Example (5)) were put into water and quenched to obtain a substrate of the present invention and a comparative example substrate.

斯くして得た本発明基板及び比較例基板について耐力を
測定した結果は第2図に示す通りであった。
The yield strength of the thus obtained substrates of the present invention and comparative substrates was measured, and the results were as shown in FIG.

第2図よシ明らかの如く本発明基板は耐力が7−5に9
fnnn−2以上の値を示し十分に蓄電池用基板として
使用することが出来た。これに対し比較例基板は7.5
に9fm−2に達せず蓄電池用基板として使用すること
が出来なかった。
As is clear from Figure 2, the yield strength of the substrate of the present invention is 7-5 to 9.
It showed a value of fnnn-2 or higher and could be used satisfactorily as a storage battery substrate. On the other hand, the comparative example board had 7.5
It could not reach 9fm-2 and could not be used as a storage battery substrate.

以上詳述し7’j如く本発明方法によれば優れた機械的
強度を有するため、充放電のサイクルを繰返すも伸びを
生せず従って蓄電池を長期使用するも短絡をおこすこと
ない等顕著な効果を有する。
As detailed above and as described in Section 7'j, the method of the present invention has excellent mechanical strength, so it does not elongate even after repeated charging and discharging cycles, and therefore, even when the storage battery is used for a long period of time, it does not cause short circuits. have an effect.

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

第1図は本発明方法における熱処理温度と耐力との関係
曲線図、第2図は本発明方法における急冷温度と耐力と
の関係曲線図である。 出願人代理人 弁理士 鈴 江 武 彦(P山°↓5M
) rl護 (zJJJ” ’+6M ) 17 phJ手続補正書 昭和 チ9.6と7日 特許庁長官 若 杉 和 夫 殿 ■、事件の表示 特願昭58− ’116509号 2・ 発明の名称 鉛蓄↑ト曹m用21(板の製造方法 3、補正をする者 事件との関係 特g=111.1刊卯人(538’)占
tり市池株式会社 4、代理人 6、補正のヌ]象 明細書 7、補正の内容 (11明細書第2頁第10行において「sp」とあるを
rsbJと訂正する。
FIG. 1 is a curve diagram showing the relationship between heat treatment temperature and yield strength in the method of the present invention, and FIG. 2 is a curve diagram showing the relationship between quenching temperature and yield strength in the method of the present invention. Applicant's representative Patent attorney Takehiko Suzue (Pyama°↓5M
) rl protection (zJJJ” '+6M) 17 phJ procedural amendments Showa Chi September 6th and 7th Mr. Kazuo Wakasugi, Commissioner of the Patent Office■, Indication of the case Patent application No. 116509 No. 116509 of 1988 2. Name of the invention: Lead acid ↑ Toso M 21 (Manufacturing method of board 3, relationship with the case of the person making the amendment Special g = 111.1 Published by Uto (538') Urashi Ichiike Co., Ltd. 4, Agent 6, No. of the amendment ] Specification 7, Contents of amendment (11 In the specification, page 2, line 10, "sp" is corrected to rsbJ.

Claims (1)

【特許請求の範囲】[Claims] 連続鋳造圧延により製造したSb 2.1〜4.5 m
10 、 As Ool 5〜0.2’ 5 rrVl
o 、残部Pbからなる鉛合金圧延板を打抜きあるいは
エキスバンド等の機械加工をする前あるいは後に230
°〜240℃にて5〜20分間熱処理した後00〜40
℃の水中にて急冷せしめることを特徴とする鉛蓄電池用
基板の製造方法。
Sb manufactured by continuous casting and rolling 2.1 to 4.5 m
10, As Ool 5~0.2' 5 rrVl
o, 230 before or after machining, such as punching or expanding a rolled lead alloy plate consisting of the remainder Pb.
After heat treatment at °~240℃ for 5~20 minutes 00~40
A method for manufacturing a lead-acid battery substrate, characterized by rapidly cooling it in water at ℃.
JP58116509A 1983-06-28 1983-06-28 Manufacture of substrate for lead storage battery Pending JPS609062A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58116509A JPS609062A (en) 1983-06-28 1983-06-28 Manufacture of substrate for lead storage battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58116509A JPS609062A (en) 1983-06-28 1983-06-28 Manufacture of substrate for lead storage battery

Publications (1)

Publication Number Publication Date
JPS609062A true JPS609062A (en) 1985-01-18

Family

ID=14688898

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58116509A Pending JPS609062A (en) 1983-06-28 1983-06-28 Manufacture of substrate for lead storage battery

Country Status (1)

Country Link
JP (1) JPS609062A (en)

Similar Documents

Publication Publication Date Title
JP5140704B2 (en) Alloys for thin positive grids for lead-acid batteries and methods for making this grid
JP2002526646A (en) Alloy for battery grid
JP2011026656A (en) Aluminum alloy foil for lithium ion secondary battery and method for producing the same
US3929513A (en) Lead alloy products
JP2002373661A (en) Silver-barium lead alloy for lead batteries and grids
JPS58123862A (en) Manufacture of copper alloy for lead material for semiconductor apparatus
CN115572857B (en) High-performance high-copper alloy and preparation method thereof
JPS609061A (en) Manufacture of lead alloy plate for lead storage battery substrate
JPS609062A (en) Manufacture of substrate for lead storage battery
JPH06179936A (en) Negative electrode material for aluminum battery
JP2012241232A (en) Rolled copper alloy foil and current collector for secondary battery using the same
JP2005510628A5 (en)
JPS60220561A (en) Manufacturing method of lead-based alloy for battery electrode plate
US2897107A (en) Annealing properties of copper
MXPA04004943A (en) Thermo-mechanical treated lead alloys.
JPH03140444A (en) Manufacture of beryllium copper alloy member
JPS6074266A (en) Manufacture of lattice substrate for lead storage battery
US4035556A (en) Lead base alloy for use in a storage battery grid
CN108193111A (en) A kind of magnesium-rare earth anode material and preparation method thereof
JPS62250136A (en) Copper alloy terminal and connector
US3008853A (en) Process for the treatment of alloys
JPS58204165A (en) Manufacture of lead alloy member
JPS6386267A (en) Manufacture of grid and grid sheet of lead acid battery
CN121992253A (en) A ductile aluminum alloy and aluminum foil
JPH0580543B2 (en)