JPS60243973A - Nonaqueous electrolyte battery - Google Patents

Nonaqueous electrolyte battery

Info

Publication number
JPS60243973A
JPS60243973A JP10083084A JP10083084A JPS60243973A JP S60243973 A JPS60243973 A JP S60243973A JP 10083084 A JP10083084 A JP 10083084A JP 10083084 A JP10083084 A JP 10083084A JP S60243973 A JPS60243973 A JP S60243973A
Authority
JP
Japan
Prior art keywords
battery
solvent
nonaqueous electrolyte
methyldioxolane
propylene carbonate
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
JP10083084A
Other languages
Japanese (ja)
Other versions
JPH0560230B2 (en
Inventor
Sanehiro Furukawa
古川 修弘
Seiji Yoshimura
精司 吉村
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.)
Sanyo Electric Co Ltd
Sanyo Denki Co Ltd
Original Assignee
Sanyo Electric Co Ltd
Sanyo Denki 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 Sanyo Electric Co Ltd, Sanyo Denki Co Ltd filed Critical Sanyo Electric Co Ltd
Priority to JP10083084A priority Critical patent/JPS60243973A/en
Publication of JPS60243973A publication Critical patent/JPS60243973A/en
Publication of JPH0560230B2 publication Critical patent/JPH0560230B2/ja
Granted 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
    • H01M6/00Primary cells; Manufacture thereof
    • H01M6/14Cells with non-aqueous electrolyte
    • H01M6/16Cells with non-aqueous electrolyte with organic electrolyte
    • H01M6/162Cells with non-aqueous electrolyte with organic electrolyte characterised by the electrolyte
    • H01M6/164Cells with non-aqueous electrolyte with organic electrolyte characterised by the electrolyte by the solvent

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

PURPOSE:To obtain a nonaqueous electrolyte battery whose discharge performance at low temperature after storage is good by using a mixture of propylene carbonate and 2-methyldioxolane as a solvent of nonaqueous electrolyte. CONSTITUTION:A mixed solvent of propylene carbonate and 2-methyldioxolane, for example, having a mixing ratio of 1:1, is used as a solvent. for example, 1mol/l of lithium perchlorate is dissolved in the mixed solvent to use as electrolyte. For example, a positive electrode is prepared by mixing carbon powder as conductor and fluorine resin powder as binder to heat-treated manganese dioxide active material, and molding the mixture, then heating the molded mix. A negative electrode is prepared by punching rolled lithium plate in a specified dimension.

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それ
らの合金を活物質とする負極と、金属の酸化物、硫化物
、ハロゲン化物などを活物質とする正極と、溶媒と溶質
とからなる非水電解液とを備えた非水電解液電池に係り
、特に非水電解液の改良に関するものである。
[Detailed Description of the Invention] (A) Industrial Application Field The present invention relates to a negative electrode that uses light metals such as lithium and sodium or alloys thereof as active materials, and metal oxides, sulfides, halides, etc. as active materials. The present invention relates to a non-aqueous electrolyte battery comprising a positive electrode and a non-aqueous electrolyte comprising a solvent and a solute, and particularly relates to improvements in the non-aqueous electrolyte.

(ロ)従来技術 この種電池に用いられる非水電解液を構成する溶媒及び
溶質として種々のものが提案されている。具体的には、
例えは特公昭57−32866号公報に開示されている
ように、溶媒とし、Tプロピレンカーボネート、γ−ブ
チロラクトン、シメトキノコータン、ジオキソラン、テ
トラハでドロフランなと、又溶、質として過塩素酸リチ
ウム、ポウフッ化リチウムなとが知られている。
(B) Prior Art Various solvents and solutes have been proposed for forming the non-aqueous electrolyte used in this type of battery. in particular,
For example, as disclosed in Japanese Patent Publication No. 57-32866, the solvent is T-propylene carbonate, γ-butyrolactone, cymethonine-butane, dioxolane, tetraha, and dorofuran, and the solvent is lithium perchlorate. Lithium fluoride is known.

さて、近年に至ってはこの種電池の適用分野の拡大に伴
い電池特性の改善が要望されでおり、その一つとして保
存後の低温下における放電特性の向上が望まれている。
Now, in recent years, as the fields of application of this type of battery have expanded, there has been a demand for improvements in battery characteristics, and one of these is the desire to improve discharge characteristics at low temperatures after storage.

くハ)発明の目的 本発明は非水電解液を改良して保存後の低温下における
放電特性に優れた非水電解液電池、を提供することを目
的とする。
c) Purpose of the Invention The object of the present invention is to provide a non-aqueous electrolyte battery which improves the non-aqueous electrolyte and has excellent discharge characteristics at low temperatures after storage.

(ニ)発明の構成 本発明はリチウム、ナトリウムなとの軽金属或いはそれ
らの合金を活物質とする負極と、正極と、溶媒と溶質と
からなる非水電解液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2−メチルジオキソランと
を含む混合溶媒であることを特徴とする非水電解液電池
にある。
(D) Structure of the Invention The present invention comprises a negative electrode having a light metal such as lithium or sodium or an alloy thereof as an active material, a positive electrode, and a non-aqueous electrolyte comprising a solvent and a solute. A non-aqueous electrolyte battery characterized in that the solvent is a mixed solvent containing propylene carbonate and 2-methyldioxolane.

(ホ)実施例 以下本発明の実施例について詳述する。(e) Examples Examples of the present invention will be described in detail below.

実施例 溶媒としてブロビレンカーポネー)1Pc)と2−メチ
ルジオキソラン(2Me −DOXL)とを混合比1゛
1で混合した混合溶媒を用い、この混合溶媒に溶質とし
て過塩素酸リチウム(LiCIO4)を1モル/rL溶
解したものを電解液とする。
As an example solvent, a mixed solvent of brobylene carbonate (1Pc) and 2-methyldioxolane (2Me-DOXL) at a mixing ratio of 1:1 was used, and lithium perchlorate (LiCIO4) was added as a solute to this mixed solvent. The solution containing 1 mol/rL is used as an electrolytic solution.

導電剤としてのカーボン粉末及び結着剤としてのフッ素
樹脂粉末とを85:10:5の重量比で混合した混合物
を加圧成形し250〜350℃で熱処理し11−ものを
用い、又負極はリチウム圧延板を所定寸法に打抜いたも
のを用いて径20.0mm、厚み2.5+nmX電池容
量120mA)]の本発明電池(A)を作成した。
A mixture prepared by mixing carbon powder as a conductive agent and fluororesin powder as a binder at a weight ratio of 85:10:5 was pressure-molded and heat-treated at 250 to 350°C to obtain a 11-type product, and the negative electrode was A battery (A) of the present invention having a diameter of 20.0 mm, a thickness of 2.5+ nm, and a battery capacity of 120 mA was prepared by punching a lithium rolled plate into predetermined dimensions.

比較例 次に本発明電池の優位性を調へるために、溶媒としてプ
ロピレンカーボネート(PC)と・ジオキソラン(DO
XL)とを1=1の混合比で混合した混合溶媒を用い、
この混合溶媒に溶質とし−(過塩素酸リチウム(L I
Cl oJを1モル/Q溶解したるものを電解液とする
比較電池<B)を作成した。尚、比較電7112(B)
は電解液を除いて他は本発明電池と同様である。
Comparative Example Next, in order to examine the superiority of the battery of the present invention, propylene carbonate (PC) and dioxolane (DO) were used as solvents.
XL) at a mixing ratio of 1=1,
As a solute in this mixed solvent - (lithium perchlorate (LI
A comparative battery <B) was prepared using an electrolyte in which 1 mol/Q of CloJ was dissolved. In addition, comparison electrician 7112 (B)
The battery is the same as the battery of the present invention except for the electrolyte.

第1図及び第2図はこれらの電池の放電特性図であって
、第1図は電池組立後、直ちに一20°Cにおいて3に
Ωの定抵抗で放電した時の放電特性図、第2図は電池組
立後、60°Cで3ケ月間保存した後、−20°Cにお
いて3にΩの定抵抗で放電した時の放電特性図である。
Figures 1 and 2 are discharge characteristic diagrams of these batteries. Figure 1 is a discharge characteristic diagram when the battery is immediately discharged at -20°C with a constant resistance of 3Ω after assembly; The figure is a discharge characteristic diagram when the battery was stored at 60°C for 3 months after assembly and then discharged at -20°C with a constant resistance of 3Ω.

第1図及び第2図から明白なるように、電池組立直後の
放電特性では本発明電池の優位性はそれほど認められな
いが、保存後の低温トにお()る放電特性では本発明電
池の優位性かより顕著である。
As is clear from FIGS. 1 and 2, the battery of the present invention does not have much superiority in the discharge characteristics immediately after battery assembly, but the battery of the present invention does not have much superiority in the discharge characteristics at low temperatures after storage. The advantage is more obvious.

下表は本発明電池<A)と比較電池(B)に用いた各電
解液の調整直後の粘度及び60°C53ケ月保存後の粘
度を示す。
The table below shows the viscosity of each electrolytic solution used in the invention battery <A) and the comparative battery (B) immediately after preparation and after storage at 60° C. for 53 months.

本発明電池が保存後の低温下にお()る放電特性に優れ
るという理由は、上表の結果から、bかるように上記名
電解液の組成において、一つの溶媒としてレオキシラン
を用いた場合には保存に伴いゲル化して粘度が高くなり
電導度が低下するのに対し、2−メチルジオキソランは
メチル基が立体障害の役目を果たしてゲル化が進まず初
期の粘度を維持していることが型費な要因と考えられる
The reason why the battery of the present invention has excellent discharge characteristics at low temperatures after storage is based on the results in the table above. While 2-methyldioxolane gels during storage, increasing its viscosity and decreasing its conductivity, the methyl group of 2-methyldioxolane acts as a steric hindrance, preventing gelation from proceeding and maintaining its initial viscosity. This is thought to be a cost factor.

又、第3図は本発明電池に用いた電解液の混合溶媒の混
合比と、電池組立後60℃C3ケ月保存した後に放電し
た際の放電容量との関係を示し、第3図より混合比率の
好適な範囲はpc/ 2Me−DOXL比が70〜20
/ 30〜80であると云える。
In addition, Figure 3 shows the relationship between the mixing ratio of the mixed solvent of the electrolyte used in the battery of the present invention and the discharge capacity when the battery was stored at 60°C for 3 months after assembly. The preferred range is a pc/2Me-DOXL ratio of 70 to 20.
/ It can be said that it is between 30 and 80.

(/\〉 発明の効果 丘述した如く、本発明によれは保存後の低温放電特性に
優れた非水電解液電池を祠・ることかできるものであり
、この種電池の用途拡大に資するところ極めて犬である
(/\〉 Effects of the Invention As mentioned above, the present invention makes it possible to create a nonaqueous electrolyte battery that has excellent low-temperature discharge characteristics after storage, and contributes to expanding the uses of this type of battery. It's very much a dog.

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

第1図及び第2図は電池の放電特性図−rあ杓、第1図
は低温下における初期放電特性図、第2図は保存後の低
温下における放電特性図である。第3図は溶媒の混合比
と保存後の低温放電時の放電容量との関係を示す図であ
る。 (A>・・本発明電池、(B)・・比較電池。 出願人 三洋電機株式会社 代理人 弁理士 佐野静失
1 and 2 are discharge characteristic diagrams of the battery, FIG. 1 is an initial discharge characteristic diagram at low temperatures, and FIG. 2 is a discharge characteristic diagram at low temperatures after storage. FIG. 3 is a diagram showing the relationship between the mixing ratio of solvents and the discharge capacity during low-temperature discharge after storage. (A>...Battery of the present invention, (B)...Comparison battery. Applicant: Sanyo Electric Co., Ltd. Agent, Patent Attorney: Shizuki Sano

Claims (1)

【特許請求の範囲】[Claims] ■リチウム、ナトリウムなどの軽金属或いはそれらの合
金を活物質とする負極と、正極と、溶媒と溶質とからな
る非水電解液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2=メチルジオキソランとを含む
混合溶媒であることを特徴とする非水電解液電池。
■It is equipped with a negative electrode whose active material is a light metal such as lithium or sodium or an alloy thereof, a positive electrode, and a non-aqueous electrolyte consisting of a solvent and a solute, where the solvent is propylene carbonate and 2=methyldioxolane. A non-aqueous electrolyte battery characterized by being a mixed solvent containing.
JP10083084A 1984-05-18 1984-05-18 Nonaqueous electrolyte battery Granted JPS60243973A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10083084A JPS60243973A (en) 1984-05-18 1984-05-18 Nonaqueous electrolyte battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10083084A JPS60243973A (en) 1984-05-18 1984-05-18 Nonaqueous electrolyte battery

Publications (2)

Publication Number Publication Date
JPS60243973A true JPS60243973A (en) 1985-12-03
JPH0560230B2 JPH0560230B2 (en) 1993-09-01

Family

ID=14284233

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10083084A Granted JPS60243973A (en) 1984-05-18 1984-05-18 Nonaqueous electrolyte battery

Country Status (1)

Country Link
JP (1) JPS60243973A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2021069923A1 (en) * 2019-10-10 2021-04-15 Mexichem Fluor S.A. De C.V. Composition

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2021069923A1 (en) * 2019-10-10 2021-04-15 Mexichem Fluor S.A. De C.V. Composition
CN114555575A (en) * 2019-10-10 2022-05-27 墨西哥氟石股份公司 Composition comprising a metal oxide and a metal oxide
CN114555575B (en) * 2019-10-10 2024-08-20 墨西哥氟石股份公司 Composition and method for producing the same

Also Published As

Publication number Publication date
JPH0560230B2 (en) 1993-09-01

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Legal Events

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EXPY Cancellation because of completion of term