JP2002151137A - Electrolyte for lead-acid battery - Google Patents

Electrolyte for lead-acid battery

Info

Publication number
JP2002151137A
JP2002151137A JP2000338586A JP2000338586A JP2002151137A JP 2002151137 A JP2002151137 A JP 2002151137A JP 2000338586 A JP2000338586 A JP 2000338586A JP 2000338586 A JP2000338586 A JP 2000338586A JP 2002151137 A JP2002151137 A JP 2002151137A
Authority
JP
Japan
Prior art keywords
electrolyte
main component
lead
electromotive force
sulfuric acid
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
Application number
JP2000338586A
Other languages
Japanese (ja)
Other versions
JP3516393B2 (en
Inventor
Emiko Mitsuyama
恵美子 光山
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to JP2000338586A priority Critical patent/JP3516393B2/en
Publication of JP2002151137A publication Critical patent/JP2002151137A/en
Application granted granted Critical
Publication of JP3516393B2 publication Critical patent/JP3516393B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • 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

  • Secondary Cells (AREA)

Abstract

PROBLEM TO BE SOLVED: To solve problems that sulfate is produced in an electrolyte containing sulfuric acid as the main component when charging/discharging cycles are repeated, resulting in drop in electromotive force, drop in performance, and short life, and dispersion in electromotive force is produced by temperature change, causing the start failure of an engine in use in the coldest season or in a cold district. SOLUTION: Without using sulfuric acid as the main component of the electrolyte, an electrolyte containing a composition of a light metal sulfate, which is an environment-friendly, weakly acidic electrolyte, as the main component, and also containing small amounts of ammonium borofluoride and nicotine amide mixed in pure water is used.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は産業用、民生用の鉛
蓄電池の電解液に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an electrolyte for an industrial and consumer lead storage battery.

【0002】[0002]

【従来の技術】鉛を電極主原料とし、硫酸水溶液を電解
質とする鉛蓄電池の電解液は蒸留水60.8%と硫酸液
39.2%で組成され、完全充電のときの比重は20℃
において1.280であり、その鉛蓄電池は電解液投入
時のエネルギー密度105%の電気容量で、約1.8年
の寿命である。
2. Description of the Related Art The electrolyte of a lead-acid battery using lead as the main electrode material and sulfuric acid aqueous solution as the electrolyte is composed of 60.8% of distilled water and 39.2% of sulfuric acid, and has a specific gravity of 20 ° C. when fully charged.
Is 1.280, and the lead storage battery has an electric capacity of 105% in energy density when the electrolyte is charged, and has a life of about 1.8 years.

【0003】[0003]

【発明が解決しようとする課題】充電、放電のサイクル
回数が増すことで鉛と硫酸の化学反応により硫酸塩が生
成するため、起電力が低下すると共に充電、放電のサイ
クル時に電解質の内部抵抗を増加させ鉛蓄電池の性能低
下と寿命短縮を来し、又、気温変化で起電力にバラツキ
を生じ、25℃程度の気温ては化学反応が活発に進行し
て放電は良好であるが、気温がマイナス1℃下がるごと
に化学反応が鈍化し起電力が1アンペアづつ下がり、鉛
蓄電池の電気容量も減少するため、マイナス10℃以下
の環境下では起電力が大巾に低下し、既存の希硫酸電解
液バッテリーでは厳冬期や寒冷地で自動車のエンジン起
動不良等の問題がある。又、急速充電を行う場合、電解
液の液温が15〜60℃に急上昇するため短時間での急
速充電はできない。
As the number of charge / discharge cycles increases, sulfate is generated by the chemical reaction between lead and sulfuric acid, so that the electromotive force is reduced and the internal resistance of the electrolyte is reduced during charge / discharge cycles. This leads to a decrease in the performance and life of the lead-acid battery, and a variation in the electromotive force due to a change in temperature. At a temperature of about 25 ° C., the chemical reaction proceeds actively and the discharge is good. Each time the temperature drops by -1 ° C, the chemical reaction slows down, the electromotive force drops by 1 ampere, and the electric capacity of the lead storage battery also decreases. Electrolyte batteries have problems such as poor engine starting of automobiles in severe winters and cold regions. In addition, when performing rapid charging, rapid charging cannot be performed in a short time because the temperature of the electrolytic solution rapidly rises to 15 to 60 ° C.

【0004】本発明は電解質を弱酸性にすることで毒性
と腐食性がない取扱いが安全な又、厳冬期や寒冷地で起
電力が低下しない性能の良い鉛蓄電池を提供すると共
に、急速充電を可能にすることを目的とする。
[0004] The present invention provides a lead-acid battery which is safe to handle without toxicity and corrosiveness by making the electrolyte weakly acidic, has a high performance in which electromotive force does not decrease in a severe winter or in a cold region, and provides rapid charging. The purpose is to make it possible.

【0005】[0005]

【課題を解決するための手段】上記目的を達成するため
本発明は鉛蓄電池の電解液の主成分として硫酸を一切使
用せず、環境に優しい弱酸性電解質である硫酸軽金属塩
の組成物を主成分として用い、これに少量のホウフッ化
アンモニウムとニコチンアマイドを水溶させた。
According to the present invention, there is provided a lead storage battery comprising a composition of a light metal salt of sulfuric acid which is an environment-friendly weakly acidic electrolyte without using sulfuric acid as a main component of the electrolyte. As components, a small amount of ammonium borofluoride and nicotine amide were dissolved in water.

【0006】[0006]

【実施例】不銹性ステンレス材製や、PVC材をコーテ
ィングした水槽で、攪拌機を有する攪拌槽と、濾過機を
有する沈殿槽及び貯蔵槽を連設し、常温常圧下で、純水
1000lに硫酸アルミニウム100〜115Κg、硫
酸マグネシウム200〜230Κg、ホウフッ化アンモ
ニウム1〜2Κg、ニコチンアマイド1〜2Κgを計量
して混合攪拌し、順次に攪拌槽、沈殿槽を経て貯蔵槽へ
保管する。
EXAMPLE A water tank made of a stainless steel material or coated with a PVC material, a stirring tank having a stirrer, a sedimentation tank having a filter, and a storage tank are connected in series, and the pressure is adjusted to 1000 liters of pure water under normal temperature and normal pressure. 100 to 115 g of aluminum sulfate, 200 to 230 g of magnesium sulfate, 1 to 2 g of ammonium borofluoride, and 1 to 2 g of nicotine amide are weighed, mixed and stirred, and sequentially stored in a storage tank via a stirring tank and a precipitation tank.

【0007】このようにして生成された電解質の比重は
1.150、pН2.5に維持され、電位は1.8Vで
あつた。
[0007] The specific gravity of the electrolyte thus produced was maintained at 1.150, p 電位 2.5, and the potential was 1.8 V.

【0008】[0008]

【実施例】本発明に係る電解液を鉛蓄電池の廃液と交換
したとき、表1及び表2に示すように電解液投入時のエ
ネルギー密度105%の電気容量が25〜95%向上し
又、鉛蓄電池の耐用年数が従来の電解液を用いたものと
比べ約3倍の4.0年〜4.5年に延長された。
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS As shown in Tables 1 and 2, when the electrolytic solution according to the present invention is replaced with the waste liquid of a lead storage battery, the electric capacity at the energy density of 105% at the time of supplying the electrolytic solution is improved by 25 to 95%. The service life of the lead-acid battery has been extended to 4.0 to 4.5 years, which is about three times as long as that using the conventional electrolyte.

【0009】[0009]

【実施例】本発明に係る電解液を60分で急速充電した
とき、表3に示すように液温は15〜35℃上昇したに
過ぎず、従来の電解液と比べきわめて短時間で急速充電
が可能となつた。即ち、従来の電解質を用いた場合、陰
極板の極性転換が充電が80%以上進行したとき、プラ
ス電圧からマイナス電圧へ転換するのに対し、本発明に
おいては充電が35%したときからマイナス電圧へ転換
され、従って従来品に比べ約3分の1に短縮された時分
で急速充電ができた。
EXAMPLE When the electrolyte according to the present invention was rapidly charged in 60 minutes, the temperature of the solution only increased by 15 to 35 ° C. as shown in Table 3, and was rapidly charged in an extremely short time as compared with the conventional electrolyte. Has become possible. That is, in the case of using the conventional electrolyte, when the polarity change of the cathode plate progresses by 80% or more, the voltage is changed from the positive voltage to the negative voltage. The battery was quickly charged in a time that was reduced to about one third of that of the conventional product.

【0010】[0010]

【発明の効果】 電解液がpН2.5の弱酸性に維持
され、毒性と腐食性がなく、取扱いが安全であり又、電
位が1.8Vに維持され安定した給電ができる。 充電、放電のサイクル寿命が従来品に比べ約3倍に
なった。 厳冬期や寒冷地でのマイナス45℃から灼熱の50
℃の間の温度変化の下でも化学反応が順調に進行するた
め起電力の低下がなく鉛蓄電池の性能が大巾に向上し
た。 従来品に比べ約3倍の速度で急速充電できた。
According to the present invention, the electrolyte is maintained at a weak acidity of pН2.5, there is no toxicity and no corrosiveness, the handling is safe, and the potential is maintained at 1.8V, so that a stable power supply can be performed. The cycle life of charging and discharging is about three times that of the conventional product. 50 intense from minus 45 degrees Celsius in severe winter or cold region
Even under a temperature change between ℃, the chemical reaction proceeded smoothly, so that the electromotive force did not decrease and the performance of the lead storage battery was greatly improved. It was able to charge quickly about three times faster than conventional products.

【0011】[0011]

【表1】 [Table 1]

【0012】[0012]

【表2】 [Table 2]

【0013】[0013]

【表3】 [Table 3]

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】純水100重量部に対し、硫酸アルミニウ
ム10.0〜11.5重量部、硫酸マグネシウム20.
0〜23.0重量部、ホウフッ化アンモニウム0.10
〜0.20重量部及びニコチンアマイド0.10〜0.
20重量部を混合した組成物から成る鉛蓄電池の電解
液。
(1) 10.0 to 11.5 parts by weight of aluminum sulfate;
0 to 23.0 parts by weight, ammonium borofluoride 0.10
-0.20 parts by weight and nicotine amide 0.10-0.
An electrolytic solution for a lead storage battery comprising a composition in which 20 parts by weight are mixed.
JP2000338586A 2000-11-07 2000-11-07 Lead-acid battery electrolyte Expired - Fee Related JP3516393B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2000338586A JP3516393B2 (en) 2000-11-07 2000-11-07 Lead-acid battery electrolyte

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2000338586A JP3516393B2 (en) 2000-11-07 2000-11-07 Lead-acid battery electrolyte

Publications (2)

Publication Number Publication Date
JP2002151137A true JP2002151137A (en) 2002-05-24
JP3516393B2 JP3516393B2 (en) 2004-04-05

Family

ID=18813780

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2000338586A Expired - Fee Related JP3516393B2 (en) 2000-11-07 2000-11-07 Lead-acid battery electrolyte

Country Status (1)

Country Link
JP (1) JP3516393B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008105559A1 (en) * 2007-02-27 2008-09-04 Shin-Kobe Electric Machinery Co., Ltd. Lead storage battery
WO2018105067A1 (en) * 2016-12-07 2018-06-14 日立化成株式会社 Lead acid storage battery

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008105559A1 (en) * 2007-02-27 2008-09-04 Shin-Kobe Electric Machinery Co., Ltd. Lead storage battery
JP2008210698A (en) * 2007-02-27 2008-09-11 Shin Kobe Electric Mach Co Ltd Lead storage battery
WO2018105067A1 (en) * 2016-12-07 2018-06-14 日立化成株式会社 Lead acid storage battery
JP6388094B1 (en) * 2016-12-07 2018-09-12 日立化成株式会社 Lead acid battery

Also Published As

Publication number Publication date
JP3516393B2 (en) 2004-04-05

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