JPS59177864A - Electrode material for lead-acid battery - Google Patents
Electrode material for lead-acid batteryInfo
- Publication number
- JPS59177864A JPS59177864A JP58053303A JP5330383A JPS59177864A JP S59177864 A JPS59177864 A JP S59177864A JP 58053303 A JP58053303 A JP 58053303A JP 5330383 A JP5330383 A JP 5330383A JP S59177864 A JPS59177864 A JP S59177864A
- Authority
- JP
- Japan
- Prior art keywords
- lead
- corrosion resistance
- acid battery
- electrode material
- strength
- 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.)
- Granted
Links
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/64—Carriers or collectors
- H01M4/66—Selection of materials
- H01M4/68—Selection of materials for use in lead-acid accumulators
- H01M4/685—Lead alloys
-
- 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
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Cell Electrode Carriers And Collectors (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は鉛蓄電池1こおける電極材として強度と耐食性
にすぐれ、かつ充電完了時の電流値か小さいことを特徴
とするpb金合金電極材tこ関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a PB gold alloy electrode material which is excellent in strength and corrosion resistance as an electrode material in a lead-acid battery, and is characterized by a small current value at the end of charging.
鉛蓄電池用電極材は現在名種々のものか提案されている
か広く用いられているものはPblこ3〜5重ffi%
程度のSbを添加したものとpbに005〜01重ft
%程度のCaを添加したものである。鉛蓄電池用電極材
に要求される性質としては適当な強さと耐食性および充
電完了時の電流か小さく減液が少ないことか挙げられ、
格子などへの適用については鋳造性あるいは加工性もま
た要求される。上記のpb−Sb合金は強さにすぐれる
か耐食性、減液の面で満足しつるものでない。一方pb
−Ca合金は減液の而てすぐれているか耐食性特に深い
充放電をくり返した時の耐食性ζこ難かある。There are currently various electrode materials for lead-acid batteries that have been proposed or widely used.
0.005 to 0.01 weight ft to PB with approximately Sb added
% of Ca is added. The properties required for electrode materials for lead-acid batteries include appropriate strength and corrosion resistance, as well as a small current at the end of charging and little loss of liquid.
Castability or workability is also required for applications such as grids. The above-mentioned pb-Sb alloys have excellent strength, but are not satisfactory in terms of corrosion resistance and liquid reduction. On the other hand pb
-Ca alloy is excellent in liquid reduction and has poor corrosion resistance, especially when repeated deep charging and discharging.
本発明は強度低下を招(ことな(鋳造性にすぐれたpb
−3b合金系電極材の耐食性および減液性を改善するこ
とを目的としたものである。The present invention causes a decrease in strength (PB with excellent castability).
The purpose is to improve the corrosion resistance and liquid reduction properties of -3b alloy-based electrode materials.
pb−Sb合金において耐食性および減液性を改善する
最も簡単な方法はSb含有量を多くとも2%以下Iこす
ることか考えられる。これはpb−sbの共晶組織を消
滅することによる耐食性および減液性の改善として知ら
れている。The easiest way to improve corrosion resistance and liquid reduction properties in pb-Sb alloys is to reduce the Sb content to at most 2% I. This is known to improve corrosion resistance and liquid reduction properties by eliminating the eutectic structure of pb-sb.
しかしSbの含有量を2%以下にすると強度の面で不足
であり、またSbの含有量か1%以上2%以下の範囲で
は鋳造時Iこ高温割れの発生率か高く鋳造性に関して難
かある。However, when the Sb content is less than 2%, the strength is insufficient, and when the Sb content is in the range of 1% to 2%, the incidence of hot cracking during casting is high, making it difficult to cast. be.
本発明の要点を一言で述べれば鋳造性の良いSb含有@
1.0%以下の合金を用い、強度不足の而についてア
ルカリ金属の添加fこよる組織の均一微細化をはかり改
善したものである。なおこれにより耐食性の向上また減
液性の向上も実験的検討の結果から得られた。The main points of the present invention can be summarized in a nutshell: Sb-containing @ with good castability
By using an alloy of 1.0% or less, the lack of strength was improved by making the structure uniform and finer due to the addition of alkali metal. Furthermore, as a result of experimental studies, improvements in corrosion resistance and liquid reduction properties were also obtained.
アルカリ金属についてはI、i、K、N aSRb。For alkali metals I, i, K, N aSRb.
C8かあるかRb、Csについては融点か低く添加上の
困難かあるため除いである。Li5K1Naの1種の添
加量は本発明において、05重量係以下、011重ff
i%以上であることを指定する。C8, Rb, and Cs are excluded because their melting points are low and there are difficulties in adding them. In the present invention, the amount of one kind of Li5K1Na added is below 05 weight factor, 011 weight factor
Specify that it is greater than or equal to i%.
ここで上限を05重ffi%とじたのはこれ以上の添加
は鋳造性を低下させるのみならず、耐食性、減液性1こ
ついても低下するからである。下限を0.11重ffi
%としたのはこれ以下では添加の効果か乏しく、強度の
面で不足であるゆえである。また以上の添加処理の対象
とするpb−Sb合金はSb量として0.2重量係以上
1.0重ffi%以下であることを指定する。ここでS
b量の上限を1.0重量係としたのはこれ以上のSb添
加は鋳造性を悪くするばかりでなく本発明の目的に不必
要であるからである。下限を02重ffi%とじたのは
これ以下ではLt、K、Naを添加しても強度の面で不
足であるためである。Here, the upper limit was set at 0.05 wt.ffi% because addition of more than this not only deteriorates castability, but also deteriorates corrosion resistance and liquid reduction properties. The lower limit is 0.11 times ffi
% because if it is less than this, the effect of addition is poor and the strength is insufficient. Further, the pb-Sb alloy to be subjected to the above addition treatment is specified to have an Sb content of 0.2% by weight or more and 1.0% by weight or less. Here S
The reason why the upper limit of the amount of b is set at 1.0 weight factor is that addition of more than this not only deteriorates castability but also is unnecessary for the purpose of the present invention. The reason why the lower limit is set at 0.2 times ffi% is that below this, even if Lt, K, and Na are added, the strength is insufficient.
実施例
pb−Sb合金にLi、に1Naを添加して引張強さを
測定した。第1表にその測定結果を示す。添加により約
3倍程度の強度増加が得られた。Example Tensile strength was measured by adding Li and 1Na to a pb-Sb alloy. Table 1 shows the measurement results. The addition resulted in an increase in strength of about 3 times.
次にpb−Sb合金ニLi、K、Naを添加したものを
20mA/枚、240hr陽極酸化させ(20℃、硫酸
比重1.28 ) 、他の合金組成のものと比べた。第
1表にその結果を示す。第1表からも明らかなように、
本廃明品か耐食性において優位であることが解る。Next, a pb-Sb alloy to which Li, K, and Na had been added was anodized at 20 mA/sheet for 240 hours (20°C, sulfuric acid specific gravity 1.28), and compared with other alloy compositions. Table 1 shows the results. As is clear from Table 1,
It can be seen that this scrapped product is superior in corrosion resistance.
なお腐食量についてはSb4重ff1%含有のpb−S
b合金の腐食量を100としたときの比である。Regarding the amount of corrosion, pb-S containing 4% Sb ff1%
This is the ratio when the amount of corrosion of alloy b is set to 100.
第 1 表
またpb−Sb合金にt、t、に、Naを添加したもの
の水素発生電位(0,43mA/m通電時)の測定を行
った。その結果を第2図番こ示す。Table 1 In addition, the hydrogen generation potential (at the time of current application of 0.43 mA/m) of the pb-Sb alloy to which Na was added at t and t was measured. The results are shown in Figure 2.
杢発明品は純pb、pb−Ca合金とほぼ等しい挙動を
示し、充電完了時の電流か小さく、純pb、pb−Ca
合金と同等の減液性か可能である。The invented product behaves almost the same as pure pb and pb-Ca alloys, and the current at the end of charging is small, and pure pb and pb-Ca
It is possible to achieve liquid reduction properties equivalent to alloys.
さら+cpb−3b合金)CL i、に1N aを添加
したものを格子に用いて電池を製作し、充放電サイクル
試験を行った。その結果pb−Ca合金格子を備えた電
池のような深い充放電による早期の容量低下は認められ
なかった。A battery was fabricated using a lattice made of a CPB-3B alloy (CPB-3B alloy) with 1N a added to it, and a charge/discharge cycle test was conducted. As a result, no early capacity reduction was observed due to deep charging and discharging unlike in batteries with a pb-Ca alloy lattice.
以上説明したようlこ、本発明鉛蓄電池用電極材は強度
にすぐれかつ耐食性、減液性にもすぐれると共に鋳造性
にもすぐる等工業的価直極めて大なるものである。As explained above, the electrode material for lead-acid batteries of the present invention has extremely high industrial value, such as excellent strength, corrosion resistance, liquid reduction properties, and castability.
第1図は本発明の実施例を示すpb−Sb合金へのLi
、KSNaの添加量に対する引張強さの関係曲線図、第
2図は本発明の実施例を示すp’b−Sb合金へのLi
、K、Naの添加量に対する水素発生電位の関係曲線図
である。
特許出願人
Lj、に、Noの璋カ日量 (車量%p第2図
Li、、に、Noの多永力口14 (重量%ラ307Figure 1 shows an embodiment of the present invention in which Li is applied to a pb-Sb alloy.
, a graph showing the relationship between the tensile strength and the amount of KSNa added, and FIG.
, K, and Na are added to the hydrogen generation potential. Patent applicant Lj, No's daily weight (vehicle volume %p Fig. 2 Li, , No's multi-day power mouth 14 (weight% La 307
Claims (1)
pb金合金アルカリ金属のL i、K、Nal7)1種
を重量比にして0.11〜0.5%添加することを特徴
とする鉛蓄電池用電極材。It is characterized by adding 0.11 to 0.5% by weight of one type of PB gold alloy alkali metal Li, K, Nal7) containing 0.2 to 1.0% by weight of Sb as a basic composition. Electrode material for lead-acid batteries.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58053303A JPS59177864A (en) | 1983-03-29 | 1983-03-29 | Electrode material for lead-acid battery |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58053303A JPS59177864A (en) | 1983-03-29 | 1983-03-29 | Electrode material for lead-acid battery |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59177864A true JPS59177864A (en) | 1984-10-08 |
JPH0320015B2 JPH0320015B2 (en) | 1991-03-18 |
Family
ID=12938952
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58053303A Granted JPS59177864A (en) | 1983-03-29 | 1983-03-29 | Electrode material for lead-acid battery |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59177864A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63187573A (en) * | 1987-01-29 | 1988-08-03 | Shin Kobe Electric Mach Co Ltd | Lead acid battery |
JPS63207057A (en) * | 1987-02-24 | 1988-08-26 | Shin Kobe Electric Mach Co Ltd | Lead storage battery |
GB2247344A (en) * | 1987-08-31 | 1992-02-26 | Shin Kobe Electric Machinery | Lead accumulators having improved charging properties after standing in over discharged state |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57162266A (en) * | 1981-03-31 | 1982-10-06 | Hitachi Chem Co Ltd | Electrode material for lead-acid battery |
-
1983
- 1983-03-29 JP JP58053303A patent/JPS59177864A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57162266A (en) * | 1981-03-31 | 1982-10-06 | Hitachi Chem Co Ltd | Electrode material for lead-acid battery |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63187573A (en) * | 1987-01-29 | 1988-08-03 | Shin Kobe Electric Mach Co Ltd | Lead acid battery |
JPS63207057A (en) * | 1987-02-24 | 1988-08-26 | Shin Kobe Electric Mach Co Ltd | Lead storage battery |
GB2247344A (en) * | 1987-08-31 | 1992-02-26 | Shin Kobe Electric Machinery | Lead accumulators having improved charging properties after standing in over discharged state |
GB2247344B (en) * | 1987-08-31 | 1992-06-10 | I Kabushiki Kaisha Shinj Saito | Lead accumulators |
Also Published As
Publication number | Publication date |
---|---|
JPH0320015B2 (en) | 1991-03-18 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN107881356B (en) | Positive grid alloy for lead-acid storage battery and preparation method thereof | |
US2860969A (en) | Lead-acid accumulator alloy | |
US4166155A (en) | Maintenance-free battery | |
US4137378A (en) | Calcium-strontium-lead grid alloy for use in lead-acid batteries | |
US3990893A (en) | Lead alloy for battery grid | |
US2170650A (en) | Alloy | |
US2694628A (en) | Grid metal alloy | |
JPS59177864A (en) | Electrode material for lead-acid battery | |
US4329408A (en) | Lead oxide composition for use in lead-acid batteries | |
CA1094359A (en) | Low antimonial lead alloy for making grids for use in maintenance free batteries | |
US2678341A (en) | Storage battery and grid therefor | |
US3912537A (en) | Electric storage battery grids | |
JP3113895B2 (en) | Lead alloy for storage battery | |
JP4293130B2 (en) | Positive electrode plate for lead acid battery and lead acid battery | |
JP6406458B2 (en) | Lead-acid battery, cast grid, and manufacturing method thereof | |
US4310353A (en) | Low-antimony lead alloy | |
US6114067A (en) | Corrosion resistant lead alloy for lead-acid batteries | |
Schumacher et al. | Some Physical and Metallurgical Properties of Lead‐Calcium Alloys for Storage Cell Grids and Plates | |
JP6601654B2 (en) | Control valve type lead acid battery | |
JP4502346B2 (en) | Lead-based alloys for lead-acid batteries | |
JP4093749B2 (en) | Lead-based alloys for lead-acid batteries | |
US3144356A (en) | Battery grid alloy | |
JPS6365041A (en) | Lead alloy for storage battery | |
JPS6043633B2 (en) | Grid for lead acid battery | |
JPS63141263A (en) | Lead-base alloy for storage battery |