JPS59151762A - Nonaqueous electrolyte battery - Google Patents
Nonaqueous electrolyte batteryInfo
- Publication number
- JPS59151762A JPS59151762A JP58025911A JP2591183A JPS59151762A JP S59151762 A JPS59151762 A JP S59151762A JP 58025911 A JP58025911 A JP 58025911A JP 2591183 A JP2591183 A JP 2591183A JP S59151762 A JPS59151762 A JP S59151762A
- Authority
- JP
- Japan
- Prior art keywords
- active material
- mixture
- battery
- positive electrode
- sintered
- 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
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
- H01M4/36—Selection of substances as active materials, active masses, active liquids
- H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
- H01M4/483—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides for non-aqueous cells
-
- 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)
- Inorganic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Primary Cells (AREA)
- Battery Electrode And Active Subsutance (AREA)
Abstract
Description
【発明の詳細な説明】
(イ)産業上の利用分野
本発明はリチウム、ナトリウムなどの軽金属或いはこれ
らを主体とする合金を活物質とする負極7備えた非水電
解液電池に係り、特に正極活物質の改良C二関するもの
である。Detailed Description of the Invention (a) Field of Industrial Application The present invention relates to a nonaqueous electrolyte battery having a negative electrode 7 whose active material is a light metal such as lithium or sodium, or an alloy mainly composed of these metals, and particularly relates to a positive electrode. This relates to improvement C of active materials.
(ロ)従来技術
非水電解液電池としては正極活物質として二酸化マンガ
ン、フッ化炭素χ用いた3v系が実用化に至っているが
、一方既存の銀電池や水銀電池と互換性のある1、5v
系電池の研究が盛ん仁行なわれている。この1.5v系
電池の正極活物質の中で三酸化ビスマスはエネルギー密
度が高く且放電電圧も1.4〜1.6’V’Y示し、有
望な活物質であると云える。しかしながら、三酸化ビス
マスは材料コストが約10円/AHであり、酸化第二銅
や硫化鉄に比して約10倍高く、又放電特性も二段とな
る欠点があった。(b) Conventional technology As a nonaqueous electrolyte battery, a 3V system using manganese dioxide and fluorocarbon χ as the positive electrode active material has been put into practical use, but on the other hand, 1, 5v
Research on battery systems is being actively conducted. Among the positive electrode active materials for this 1.5V battery, bismuth trioxide has a high energy density and exhibits a discharge voltage of 1.4 to 1.6'V'Y, so it can be said to be a promising active material. However, bismuth trioxide has a material cost of about 10 yen/AH, which is about 10 times higher than cupric oxide or iron sulfide, and has the disadvantage that its discharge characteristics are second-tier.
し→ 発明の目的
本発明は既存の銀電池や水銀電池と互換性に優れた特性
を有し、且安価な1.5v系の非水電解液電池を提案す
ること7目的とする。Object of the Invention The object of the present invention is to propose an inexpensive 1.5V non-aqueous electrolyte battery that has characteristics excellent in compatibility with existing silver batteries and mercury batteries.
に)発明の構成
本発明は上記目的を達成すべくなされたものにして、リ
チウム、ナトリウムなどの軽金属或いはこれらを主体と
する合金Z活物質とする負極と、ビスマス−鉄複合酸化
物を活物質とする正極と、非水電解液と!備えた非水電
解液電池を提案するものである。B) Structure of the Invention The present invention has been made to achieve the above object, and provides a negative electrode having a Z active material made of a light metal such as lithium or sodium or an alloy mainly composed of these, and a bismuth-iron composite oxide as an active material. A positive electrode and a non-aqueous electrolyte! This paper proposes a non-aqueous electrolyte battery equipped with
(ホ))実施例 以下本発明の一実施例につき詳述する。(e)) Examples An embodiment of the present invention will be described in detail below.
正極の作成例:
市販−級試薬の三酸化ビスマス(Bi205)と酸化第
二鉄(Fe2O2)と7モル比で1:2にHaし乳鉢に
て混合する。この混合物Zアルミするつぼに入れ9気中
で800℃、20時間幣成金行なった後放冷する。尚、
焼成温度については500℃位でもよいが反応速度を進
めるために高温度の方が好ましく、又焼成雰囲気につい
ては酸化雰囲気、不活性雰囲気でも良い。次いで上記焼
成物乞乳鉢で粉砕し400メツシユパスしたものを正極
活物質とする。そしてこの活物質と、導電剤としての黒
鉛粉末と、結着剤としてのフッ素樹脂粉末とン80:1
5:5(重哲比)の割合で混合し、この混合物乞成型し
た後300℃で1時間熱処理したものZ正極とする。Example of creating a positive electrode: Commercially available reagents such as bismuth trioxide (Bi205) and ferric oxide (Fe2O2) are mixed in a 7 molar ratio of 1:2 in a mortar. This mixture was placed in a Z aluminum crucible and deposited at 800° C. for 20 hours in 9 atmospheres, and then left to cool. still,
The firing temperature may be about 500°C, but a higher temperature is preferred in order to accelerate the reaction rate, and the firing atmosphere may be an oxidizing atmosphere or an inert atmosphere. Next, the material was ground in the above-mentioned firing mortar and passed through 400 meshes to be used as a positive electrode active material. This active material, graphite powder as a conductive agent, and fluororesin powder as a binder were mixed at a ratio of 80:1.
The mixture was mixed at a ratio of 5:5 (weight ratio), molded, and then heat-treated at 300° C. for 1 hour to obtain a Z positive electrode.
負極はリチウム圧延板を所定寸法に打抜いたものン用い
、又電解液はプロピレンカーボネートと1.2ジメトキ
シエタンとの等体積混合溶媒に過塩素酸リナウムン溶解
したものであり、ポリプロピレン不織布よりなるセパレ
ータに含浸して用いた。The negative electrode was a rolled lithium plate punched out to a specified size, and the electrolyte was linum perchlorate dissolved in an equal volume mixed solvent of propylene carbonate and 1.2 dimethoxyethane.A separator made of polypropylene nonwoven fabric was used as the negative electrode. It was used after being impregnated with.
電池寸法は直径11.5111+、高さ5.4調であっ
た。The battery dimensions were 11.5111+ in diameter and 5.4 in height.
図は本発明電池(Alの放電特性?示し、放電条件は2
0℃における3、6にΩ定負荷放電である。The figure shows the discharge characteristics of the battery of the present invention (Al), and the discharge conditions are 2.
3.6Ω constant load discharge at 0°C.
尚、図中(B)は正極活物質として三酸化ビスマスを単
独で用いた比較電池、又lotは正極活物質として酸化
第二鉄ン単独で用いた従来電池の場合ン夫々示す。In the figure, (B) shows a comparative battery using bismuth trioxide alone as the positive electrode active material, and lot shows a conventional battery using ferric oxide alone as the positive electrode active material.
H発明の効果
図より明白なるよう?=、本発明電池は約1.5vの放
電電圧を有し、且放電特性も二段となっておらず、既存
の銀電池や水銀電池との互換性に優れた1、5v系非水
電解液電池であると云える。加えて材料コストについて
も三酸化ビスマス単独の場合に比して低廉化が計れる。Is it clearer than the effect diagram of H invention? = The battery of the present invention has a discharge voltage of approximately 1.5V, and has no two-stage discharge characteristics, and is a 1.5V non-aqueous electrolytic battery that is highly compatible with existing silver batteries and mercury batteries. It can be said that it is a liquid battery. In addition, the material cost can be reduced compared to the case of using only bismuth trioxide.
本発明電池において放電電圧特性が安定した理由は詳か
ではないが、正極活物質yiI−X線分析したところビ
スマス−鉄初台酸化物であるB12F+11409或い
はBiFθ0δが生成しており、これらの複合酸化物が
特性向上に寄与しているものと考えられる。The reason why the discharge voltage characteristics were stable in the battery of the present invention is not clear, but when the positive electrode active material was analyzed by yiI-X rays, bismuth-iron initial oxide B12F+11409 or BiFθ0δ was formed, and these composite oxides It is thought that this contributes to the improvement of characteristics.
尚、ビスマス−鉄複合酸化物の作成に際して、実施例で
はビスマス及び鉄の酸化物を出発物質とする場合を例示
したが、それ以外に一方或いは双方を硫酸塩、硝酸塩Z
出発物質として作成することもできる。In addition, when creating a bismuth-iron composite oxide, the example uses bismuth and iron oxides as starting materials.
It can also be made as a starting material.
図面は本発明電池の放電特性7示す。
(AI・・・本発明電池、(Bl(Cl・・・比較電池
。
4g1l智へ1旧 2The drawing shows the discharge characteristics 7 of the battery according to the invention. (AI...Battery of the present invention, (Bl(Cl...Comparative battery. 4g1l To Ji 1 Old 2
Claims (1)
生体とする合金Z活物質とする負極と、ビヌマスー鉄複
合酸化物乞活物質とする正極と、非水電解液とン備えた
非水電解液電池。(2) A non-aqueous electrolyte battery comprising a negative electrode made of light metals such as lithium and sodium or an alloy Z active material containing these as living bodies, a positive electrode made of a vinylium-iron composite oxide active material, and a non-aqueous electrolyte.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58025911A JPS59151762A (en) | 1983-02-17 | 1983-02-17 | Nonaqueous electrolyte battery |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58025911A JPS59151762A (en) | 1983-02-17 | 1983-02-17 | Nonaqueous electrolyte battery |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS59151762A true JPS59151762A (en) | 1984-08-30 |
Family
ID=12178955
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58025911A Pending JPS59151762A (en) | 1983-02-17 | 1983-02-17 | Nonaqueous electrolyte battery |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59151762A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3607254A1 (en) * | 1985-03-07 | 1986-10-16 | Aisin Seiki K.K., Kariya, Aichi | MAIN CYLINDER |
JP2005534877A (en) * | 2002-07-30 | 2005-11-17 | コンチネンタル・テベス・アーゲー・ウント・コンパニー・オーハーゲー | Seal color |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5530182A (en) * | 1978-08-23 | 1980-03-03 | Sanyo Electric Co Ltd | Non-aqueous electrolyte battery |
JPS5546288A (en) * | 1978-09-28 | 1980-03-31 | Sanyo Electric Co Ltd | Nonaqueous electrolytic cell |
JPS55111068A (en) * | 1979-02-20 | 1980-08-27 | Sanyo Electric Co Ltd | Nonaqueous electrolyte battery |
JPS55111067A (en) * | 1979-02-20 | 1980-08-27 | Sanyo Electric Co Ltd | Nonaqueous electrolyte battery |
-
1983
- 1983-02-17 JP JP58025911A patent/JPS59151762A/en active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5530182A (en) * | 1978-08-23 | 1980-03-03 | Sanyo Electric Co Ltd | Non-aqueous electrolyte battery |
JPS5546288A (en) * | 1978-09-28 | 1980-03-31 | Sanyo Electric Co Ltd | Nonaqueous electrolytic cell |
JPS55111068A (en) * | 1979-02-20 | 1980-08-27 | Sanyo Electric Co Ltd | Nonaqueous electrolyte battery |
JPS55111067A (en) * | 1979-02-20 | 1980-08-27 | Sanyo Electric Co Ltd | Nonaqueous electrolyte battery |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3607254A1 (en) * | 1985-03-07 | 1986-10-16 | Aisin Seiki K.K., Kariya, Aichi | MAIN CYLINDER |
JP2005534877A (en) * | 2002-07-30 | 2005-11-17 | コンチネンタル・テベス・アーゲー・ウント・コンパニー・オーハーゲー | Seal color |
JP4907867B2 (en) * | 2002-07-30 | 2012-04-04 | コンチネンタル・テベス・アーゲー・ウント・コンパニー・オーハーゲー | Seal color |
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