JPS5987773A - organic electrolyte battery - Google Patents
organic electrolyte batteryInfo
- Publication number
- JPS5987773A JPS5987773A JP57198007A JP19800782A JPS5987773A JP S5987773 A JPS5987773 A JP S5987773A JP 57198007 A JP57198007 A JP 57198007A JP 19800782 A JP19800782 A JP 19800782A JP S5987773 A JPS5987773 A JP S5987773A
- Authority
- JP
- Japan
- Prior art keywords
- battery
- propylene carbonate
- active material
- positive
- glycol dimethyl
- 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
- H01M6/00—Primary cells; Manufacture thereof
- H01M6/14—Cells with non-aqueous electrolyte
- H01M6/16—Cells with non-aqueous electrolyte with organic electrolyte
- H01M6/162—Cells with non-aqueous electrolyte with organic electrolyte characterised by the electrolyte
- H01M6/164—Cells with non-aqueous electrolyte with organic electrolyte characterised by the electrolyte by the solvent
-
- 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
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Primary Cells (AREA)
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明はリチウム、ナトリウム、マグネシウムなどの軽
金属を活物質とする負極と、金属の酸化物、硫化物或い
はハロゲン化物などを活物質とする正極と、プロピレン
カーボネート、γ−ブチルラクトン、ジメトキシエタン
などの有機溶媒に過塩素酸リチウム、ホウフッ化リチウ
ムなどの無機塩溶質を溶解させた電解質とを備える有機
電解質電池に関するものである。[Detailed Description of the Invention] Industrial Application Field The present invention provides a negative electrode using a light metal such as lithium, sodium, or magnesium as an active material, and a positive electrode using a metal oxide, sulfide, or halide as an active material. The present invention relates to an organic electrolyte battery comprising an electrolyte in which an inorganic salt solute such as lithium perchlorate or lithium fluoroborate is dissolved in an organic solvent such as propylene carbonate, γ-butyllactone, or dimethoxyethane.
従来技術
この種電池は高電圧、高エネルギー密度を有し、且自已
放電が少ないなど故多くの利点を有しており、現在のと
ころ二酸化マンガン、フッ化炭素を正極活物質とする電
池が実用化されている。特に二酸化=ンガンは安定性、
経済性の面で優れた正極活物質と云える。Conventional technology This type of battery has many advantages such as high voltage, high energy density, and little self-discharge.At present, batteries using manganese dioxide or carbon fluoride as the positive electrode active material are in practical use. has been made into In particular, the stability of carbon dioxide,
It can be said to be an excellent positive electrode active material in terms of economic efficiency.
さて、−市電解質について云えば、一般的には溶媒とし
てプロピレンカーボネートとジメトキシエタンとの混合
溶媒が用いられているっこの理由はプロピレンカーボネ
ートは誘電率が大であるものの粘度が高いため、この粘
度を補償するために補助溶媒として粘度の低いジメトキ
シエタンを混合して用いているのである。Now, speaking of electrolytes, a mixed solvent of propylene carbonate and dimethoxyethane is generally used as a solvent.The reason for this is that although propylene carbonate has a high dielectric constant, it has a high viscosity. In order to compensate for this, dimethoxyethane, which has a low viscosity, is mixed and used as an auxiliary solvent.
ところで、補助溶媒としてのジメトキシエタンはその沸
点が1気圧において85゛Cと低いため、特に60℃以
上での電池特性に問題があるっ発明の目的
本発明は上記問題点に鑑み、30℃以上においても優れ
た電池特性を示す有機型1v?質電池を提供することを
目的とするものであるっ
発明の(1(¥成
本発明は上記し」的を達成すべくなされたものであり、
その要旨とするところは、
軽金属を活物質とする負極と、正極と、溶媒と溶質とか
らなる電解質とを備えるものであって、前記溶媒がプロ
ピレンカーボネート(PC)とジエチルグリコールジメ
チルエーテル[CHs(OCR2CH2) 20cI−
1s J の混合溶媒であることを特徴とする有機電解
質電池にある。By the way, dimethoxyethane as an auxiliary solvent has a boiling point as low as 85°C at 1 atm, so there is a problem with battery characteristics especially at temperatures above 60°C.Purpose of the Invention In view of the above problems, the present invention has been developed to The organic type 1v? exhibits excellent battery characteristics even in The purpose of the present invention is to provide a quality battery.
Its gist is that it is equipped with a negative electrode made of a light metal as an active material, a positive electrode, and an electrolyte made of a solvent and a solute, the solvent being propylene carbonate (PC) and diethyl glycol dimethyl ether [CHs(OCR2CH2 ) 20cI-
The organic electrolyte battery is characterized in that it is a mixed solvent of 1 s J .
実施例
以下本発明の実施例について詳述するっ正極は、空気中
で650℃〜430℃で熱処理した二酸化−ンガン活物
質と、導電剤としてのアセチレンブラック及び黒鉛と、
結着剤としてのフッ素樹脂粉末を85 =’ 10 :
5の重量比で混合した正極合剤を約1トン/−の圧力
で加圧成型して径約15咽、厚さ約1,1mの正極ベレ
ットとし、このペレットを250”C−3[)0℃の湿
度で焼成して正極とする。Examples Examples of the present invention will be described in detail below.The positive electrode was made of a carbon dioxide active material heat-treated at 650°C to 430°C in air, acetylene black and graphite as conductive agents,
Fluororesin powder as a binder: 85='10:
A positive electrode mixture mixed at a weight ratio of 5:5 was press-molded at a pressure of about 1 ton/- to form a positive electrode pellet with a diameter of about 15 mm and a thickness of about 1.1 m, and this pellet was made into a 250"C-3 [). The positive electrode is baked at 0°C humidity.
負極は厚み約06簡のリチウム圧延板を径約15胴に打
抜いたものを用い、又セパレークとしてはポリプロピノ
ン不繊布を用いたつ
而して、電解質はプロピレンカーボネートとジエチレン
グリコールジメチルエーテルとを混合比1:1で混合し
た混合溶媒に過塩素酸リチウムを1モル/l溶解させた
ものを用いて本発明電池(A)を作成した。The negative electrode was a lithium rolled plate with a thickness of about 0.6 mm and punched into a diameter of about 1.5 mm, and the separator was made of polypropylene nonwoven fabric.The electrolyte was a mixture of propylene carbonate and diethylene glycol dimethyl ether at a mixing ratio of 1. A battery (A) of the present invention was prepared using a mixture of 1 mol/l of lithium perchlorate dissolved in the mixed solvent prepared in step 1.
合した混合溶媒に過塩素酸リチウムを1モル/l溶解さ
せたものを用いることを除いて他は実施例と同様の比較
電池(13)を作成した。A comparative battery (13) was prepared in the same manner as in Example except that 1 mol/l of lithium perchlorate was dissolved in the mixed solvent.
発明の効W
銘1図乃至第3図は本発明電池(A)と比較電池(B)
との負荷5.6 KΩにおける電池特性比較図であり、
第1図は20゛Cでの初期放電特性、第2図は30℃で
2年保存後、30℃での放電特性、第3図は60℃で2
ケ月保存後、60℃での放電特性を夫々示す。Effects of the invention W Figures 1 to 3 show the invention battery (A) and comparative battery (B).
It is a comparison diagram of battery characteristics at a load of 5.6 KΩ with
Figure 1 shows the initial discharge characteristics at 20°C, Figure 2 shows the discharge characteristics at 30°C after 2 years of storage at 30°C, and Figure 3 shows the discharge characteristics at 60°C.
After storage for several months, the discharge characteristics at 60°C are shown.
これらの特性図よりり]白なるように、20′Cでの初
N1放電特性ではほとんど差異はないが30’C以上で
の放電の場合には本発明電泪貝A)の方が比較電池(B
)より容量の低下が少ない。As can be seen from these characteristic diagrams, there is almost no difference in the initial N1 discharge characteristics at 20'C, but in the case of discharge at 30'C or higher, the present invention's Denkigai A) is better than the comparison battery. (B
) The decrease in capacity is less than that of
この理由を考察するに、ジメトキーシエタンは前述した
ようにその沸点は1気王において850であるのに対し
、ジエチレングルコールジメチルニーデルは1気圧にお
いて162′Cであること、及び20Cでの蒸気圧につ
いてもジメトキシエクンは48 van■Igであるの
に対しジエチレングリコールジメチルエーテルは3++
mHg であることから、特に高温での放電、特性につ
いては本発明電池によれば容量の劣化が少ないと考えら
れる。Considering the reason for this, as mentioned above, the boiling point of dimethoxyethane is 850 at 1 atmosphere, whereas the boiling point of diethylene glycol dimethyl needle is 162'C at 1 atmosphere, and at 20C. The vapor pressure of dimethoxyecune is 48 van Ig, while that of diethylene glycol dimethyl ether is 3++
mHg, it is thought that the battery of the present invention will have less deterioration in capacity, especially in terms of discharge and characteristics at high temperatures.
尚、プロピレンカーボネートとジエチレングリコールジ
メチルエーテルの混合比については1:3〜3:1が好
ましい。この範囲以外、例えばプロピレンカーボネート
の量がさらに増すと粘度が高くなるため好ましくなく、
又ジエチルグリコールジメチルエーテルの量がさらに増
すとプロピレンカーボネートに比して低沸点の溶媒の割
合が増すため好′!!−シくない。The mixing ratio of propylene carbonate and diethylene glycol dimethyl ether is preferably 1:3 to 3:1. If the amount of propylene carbonate is further increased outside this range, the viscosity will increase, which is not preferable.
Also, if the amount of diethyl glycol dimethyl ether increases further, the proportion of the solvent with a lower boiling point will increase compared to propylene carbonate, which is preferable! ! -No.
図はいづれも本発りj電?lD、と比較電池との電池特
性比較図を示し、第1図は20゛Cでの初期放電特性、
第2図は60′Cで2年保存後、30℃での放電特性、
第3図は60℃で2ケ月保存後、60℃での放電特性を
夫々示す。
(A)・・・本発明電池、(B)・・・従来電池。
第V図
吟唱(hr)
第2図
第8図
357Are all the figures originally from J-den? Figure 1 shows the initial discharge characteristics at 20°C,
Figure 2 shows the discharge characteristics at 30°C after 2 years of storage at 60'C.
Figure 3 shows the discharge characteristics at 60°C after two months of storage at 60°C. (A)...Battery of the present invention, (B)...Conventional battery. Figure V chant (hr) Figure 2 Figure 8 357
Claims (1)
とからなる電解質とを備えるものであって、前記溶媒が
プロピレンカーボネートとジエチレングリコールジメチ
ルエーテルの混合溶媒テすることを特徴とする有機電解
質電池。 ■ 前記混合溶媒の混合比が1:3〜3:1であること
を特徴とする特I¥′f請求の範囲第0項記載の有機電
解質電池。[Scope of Claims] ■ A negative electrode comprising a light metal as an active material, a positive electrode, and an electrolyte comprising a solvent and a solute, characterized in that the solvent is a mixed solvent of propylene carbonate and diethylene glycol dimethyl ether. Organic electrolyte battery. (2) The organic electrolyte battery according to claim 0, characterized in that the mixing ratio of the mixed solvent is 1:3 to 3:1.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57198007A JPS5987773A (en) | 1982-11-10 | 1982-11-10 | organic electrolyte battery |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57198007A JPS5987773A (en) | 1982-11-10 | 1982-11-10 | organic electrolyte battery |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS5987773A true JPS5987773A (en) | 1984-05-21 |
Family
ID=16383954
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP57198007A Pending JPS5987773A (en) | 1982-11-10 | 1982-11-10 | organic electrolyte battery |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5987773A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6116479A (en) * | 1984-07-02 | 1986-01-24 | Sanyo Electric Co Ltd | Nonaqueous electrolyte battery |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS54115134U (en) * | 1978-01-31 | 1979-08-13 | ||
| JPS5625578A (en) * | 1979-08-08 | 1981-03-11 | Kayoko Kiuchi | Method of construction of exchanging of fence* etc* |
| JPS57174574A (en) * | 1981-04-20 | 1982-10-27 | Yoshida Kogyo Kk | Renewing of established handrail |
-
1982
- 1982-11-10 JP JP57198007A patent/JPS5987773A/en active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS54115134U (en) * | 1978-01-31 | 1979-08-13 | ||
| JPS5625578A (en) * | 1979-08-08 | 1981-03-11 | Kayoko Kiuchi | Method of construction of exchanging of fence* etc* |
| JPS57174574A (en) * | 1981-04-20 | 1982-10-27 | Yoshida Kogyo Kk | Renewing of established handrail |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6116479A (en) * | 1984-07-02 | 1986-01-24 | Sanyo Electric Co Ltd | Nonaqueous electrolyte battery |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPH0495362A (en) | Nonaqueous electrolytic battery | |
| JPS62216171A (en) | non-aqueous electrolyte battery | |
| JPS62217567A (en) | Nonaqueous electrolyte battery | |
| JP3053672B2 (en) | Manufacturing method of organic solvent secondary battery | |
| JPS6110863A (en) | Nonaqueous electrolyte batter | |
| JPS6229070A (en) | non-aqueous electrolyte battery | |
| JP3418715B2 (en) | Organic electrolyte secondary battery | |
| JPH0227664A (en) | Nonaqueous electrolyte battery | |
| JPH07130361A (en) | Non-aqueous electrolyte battery | |
| JPH01227355A (en) | Nonaqueous electrolyte battery | |
| JPS5987772A (en) | Organic electrolyte battery | |
| JPH0215568A (en) | Nonaqueous electrolyte primary battery | |
| JPS62119867A (en) | Manufacture of active material for positive electrode of battery with organic electrolytic solution | |
| JPS59128772A (en) | Nonaqueous solvent battery | |
| JPH08171937A (en) | Lithium secondary battery | |
| JPH0215566A (en) | Nonaqueous type electrolyte battery | |
| JPH1126022A (en) | Manufacturing method of lithium ion secondary battery | |
| JPS59134562A (en) | Lithium secondary cell | |
| JPS6191862A (en) | Manufacturing method of non-aqueous electrolyte battery | |
| JPH0552026B2 (en) | ||
| JPS6224569A (en) | Nonaqueous electrolyte battery | |
| JPS59165372A (en) | Nonaqueous electrolyte secondary battery | |
| JPS60249256A (en) | non-aqueous electrolyte battery | |
| JPH0665042B2 (en) | Non-aqueous electrolyte battery | |
| JPH07272714A (en) | Non-aqueous electrolyte battery |