JPS6023957A - Manufacture of nonaqueous electrolytic battery - Google Patents

Manufacture of nonaqueous electrolytic battery

Info

Publication number
JPS6023957A
JPS6023957A JP13122383A JP13122383A JPS6023957A JP S6023957 A JPS6023957 A JP S6023957A JP 13122383 A JP13122383 A JP 13122383A JP 13122383 A JP13122383 A JP 13122383A JP S6023957 A JPS6023957 A JP S6023957A
Authority
JP
Japan
Prior art keywords
positive electrode
battery
active material
electrode active
constant current
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
Application number
JP13122383A
Other languages
Japanese (ja)
Inventor
Toshio Shigematsu
重松 敏雄
Makoto Watabe
信 渡部
Koichi Sato
公一 佐藤
Masaki Nakai
中井 正樹
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.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial 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 Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP13122383A priority Critical patent/JPS6023957A/en
Publication of JPS6023957A publication Critical patent/JPS6023957A/en
Pending 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
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/06Electrodes for primary cells
    • H01M4/08Processes of manufacture

Abstract

PURPOSE:To improve the close circuit voltage characteristics and pulse characteristics as the initial discharge stage, improve productivity due to the simplification of manufacturing process, increase capacity, and stabilize battery characteristics by comprising a battery after the carbon fluoride as positive electrode active material pressurized and molded in a pellet shape is previously constant- current-discharged in an electrolyte. CONSTITUTION:When a nonaqueous electrolyic battery that uses mettalic lithium 4 as the negative electrode active material and carbon fluoride as the positive electrode active material is manufactured, constant current discharge is executed previously for the carbon fluoride as the positive electrode active material molded in a pellet shape (a) and the battery is comprised using it as a positive electrode 6. For example, after the carbon fluoride as the positive electrode active material is pressurized and molded in a pellet shape (a), it is dipped in a mixed solution composed of gamma-butyrolactone and 1,2 dimethoxy ethane as the electrolyte. While they are being slowly agitated by an agitation blade c using a lithium rod as a paired electrode b, constant current discharge is executed by connecting a power supply d. In this case, the constant current condition is set to 3-5% of total capacity.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は、金属リチウムを負極活物質とし、正極活物質
にフッ化炭素を使用する非水電解液電池に関するもので
ある。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to a non-aqueous electrolyte battery that uses metallic lithium as a negative electrode active material and fluorocarbon as a positive electrode active material.

従来・例の構成とその問題点 この種の電池は、酸化銀電池などに比較して軽量であり
、さらに2.8v程度の平坦な放電%性が得られるため
、近年各方面での応用が期待されている。
Conventional/example configurations and their problems This type of battery is lighter than silver oxide batteries and has a flat discharge rate of about 2.8V, so it has been used in various fields in recent years. It is expected.

従来、一般にこの種の電池は、正極活物質であるフン化
炭素の特性により、構成された電池の放電初期における
閉路電圧特性は、放電直後数時間後に最低電圧を示し、
更に放電深度の進行によって徐々に上昇するという傾向
を示す。
Conventionally, this type of battery generally has a closed-circuit voltage characteristic at the beginning of discharge due to the characteristics of fluorinated carbon, which is the positive electrode active material, and shows the lowest voltage several hours immediately after discharge.
Furthermore, it shows a tendency to gradually increase as the depth of discharge progresses.

この放電を開始して数時間後に閉路電圧が最低値に達し
た時の、強負荷パルス特性における電圧も最低を示す。
When the closed circuit voltage reaches the lowest value several hours after starting this discharge, the voltage in the strong load pulse characteristic also shows the lowest value.

従って、この電圧を少なくする事により、時開等のラン
グ・マラーム等強負荷特性を要求される用途において、
改良を余義なくされていた。
Therefore, by reducing this voltage, in applications that require heavy load characteristics such as Lang Malam, etc., such as time opening, etc.
Improvements were inevitable.

従来、この種の問題を解決する方法として、電池を構成
した後に、定電流放電を実施する方法が提案されている
。しかし、従来の方法で目1、次に示すような欠点を有
していた。
Conventionally, as a method for solving this type of problem, a method has been proposed in which a battery is constructed and then subjected to constant current discharge. However, the conventional method has the following drawbacks.

(1)定電流放電を全容量の3〜5%実施しなければな
ら檄限られた容積の中で3〜6%の容′1f)(ロスが
ともなう。
(1) If constant current discharge has to be carried out to 3 to 5% of the total capacity, there will be a loss of 3 to 6% of the total capacity (loss).

?)電池を構成後更に定電流放電を実施するため設備2
時間等、手間がかかりi・−タル的にコストアツブにな
る。
? ) Facility 2 for further constant current discharge after configuring the battery.
It takes time, effort, etc., and increases the cost.

−(3)短時間で実施するために電流値を上げると、開
路電圧の逆転や、リチウムの析出、ひいては電池静特性
のバラツキが発生する。
-(3) If the current value is increased in order to carry out the test in a short period of time, the open circuit voltage will reverse, lithium will be deposited, and the static characteristics of the battery will vary.

(4)電池特性の構成時の電圧、電流等の個々の特性が
バラツクため、定電流放電を実施すると容量、電圧、電
流等の特性のバラツキが更に拡大する。
(4) Since individual characteristics such as voltage and current vary when configuring battery characteristics, when constant current discharge is performed, the variations in characteristics such as capacity, voltage, and current further increase.

(6)定電流実施後、開路電圧の復帰、不良の検出等の
ため、エージングを必要とした。
(6) After implementing constant current, aging was required to restore open circuit voltage, detect defects, etc.

本発明者らは、このような電池の研究過程において、7
ノ化炭素を加圧成型して得られた時に定電流放電全実施
することにより、電池を構成してから定電流放電を実施
した時よりも、特に初期における電圧の低下を防止し、
同体積の中で最も大きな容量を得ることがわかり、この
発明を完成するに至った。
In the process of researching such batteries, the present inventors discovered 7
By carrying out constant current discharge at the time of pressure molding the carbon noride, it is possible to prevent voltage drop, especially in the initial stage, compared to when carrying out constant current discharge after constructing the battery.
It was found that the largest capacity can be obtained among the same volumes, and this invention was completed.

発明の目的 本発明は、前述した種々の問題点を解決し、放電初期に
おける閉路電圧特性、パルス特性の改良とともに、製造
工程の簡素化による量産性の向上あるいは高容量化、電
池緒特性の安定等、安価でしかも信頼性の高い非水電解
液電池を提供するものである。
Purpose of the Invention The present invention solves the various problems mentioned above, improves the closed circuit voltage characteristics and pulse characteristics at the initial stage of discharge, and improves mass productivity by simplifying the manufacturing process, increases capacity, and stabilizes battery characteristics. The present invention provides an inexpensive and highly reliable non-aqueous electrolyte battery.

発明の構成 本発明は、電池構成前に正極活物質である7ノ化炭素を
ペレット状に加圧成型したものを、電解液中であらかじ
め定電流放電させた後、電池を構成するものである。
Structure of the Invention In the present invention, carbon heptanoide, which is a positive electrode active material, is press-molded into pellets before battery construction, and the pellets are discharged at a constant current in an electrolytic solution, and then the battery is constructed. .

この製造法によれば、正極の放電は製造工程中に短時間
で実施でき簡単である。丑だ、正極活物質をあらかじめ
3〜5俸増加させておくと、負極活物質の消耗はないの
で3〜5係の容量増加を得ることができる。さらに定電
流放電を短時間で実施しても、電解液と正極活物質だけ
であるのでセパレーターの劣化がなく安定した品質の電
池が得られ、電池としての電圧、電流容量等に与える影
響が少なく、バラツキが少なくなる等の利点がある。
According to this manufacturing method, the discharge of the positive electrode can be easily performed in a short time during the manufacturing process. If you increase the positive electrode active material by 3 to 5 in advance, the negative electrode active material will not be consumed, so you can increase the capacity by 3 to 5 times. Furthermore, even if constant current discharge is performed for a short period of time, since there is only an electrolyte and a positive electrode active material, a battery of stable quality can be obtained without deterioration of the separator, and there is little effect on the voltage, current capacity, etc. of the battery. , there are advantages such as less variation.

実施例の説明 以下、本発明の詳細な説明する0 第1図に示すように、正極活物質であるフッ化炭素をペ
レット状aに加圧成型した後、電解液であるγ−ブチロ
ラクトンと1,2ジメトキシエタンとの混合液中に浸漬
し、対をなす電極すとしてリチウム棒を使用し、攪拌翼
Cでゆっくり攪拌しながら、電源dをつなぎ定電流放電
を実施する。
DESCRIPTION OF EXAMPLES The present invention will be described in detail below. As shown in FIG. , 2 dimethoxyethane, and using a lithium rod as a pair of electrodes, while stirring slowly with a stirring blade C, a power source d is connected to perform constant current discharge.

この時、定電流の条件は、全容量の3%〜S係とする。At this time, the constant current condition is 3% to S of the total capacity.

3チ以下であると前記した閉路電圧低下に対してその抑
制効果がなく、6係以上実施してもそれ以上電圧の上昇
は認められず、容量の低下のみが進行するためである。
This is because if it is 3 or less, there is no effect of suppressing the drop in the closed circuit voltage, and even if 6 or more steps are carried out, no further increase in voltage will be observed, and only a decrease in capacity will proceed.

第2図は、本発明の正極を用いたリチウム−フッ化炭素
の扁平形有機電解質電池を示す0図において、1は厚さ
0.30mmの耐有機電解液性をもったステンレス鋼板
を外径22.9+nm、高さ2.7CHnmに杓ち抜き
加工した電池ケース、2(l−j:1と同月料素材を外
径21.2mm 、 ’H%さ1.60叫に加工した封
口板、3は封目板の内面にスポット溶接した直径18職
、厚さ0.27mm 、多孔度86%のニッケル発泡体
からなる負極集電体、4は直径17胴、厚さ0.31m
mのリチウムシートからなる負極活物質で集電体3に圧
着されている。6は直径16mm。
Figure 2 shows a lithium-fluorocarbon flat organic electrolyte battery using the positive electrode of the present invention. 22.9 + nm, height 2.7 CH nm battery case, 2 (l-j: 1) and a sealing plate processed from the same material as 21.2 mm in outer diameter and 1.60 in H%; 3 is a negative electrode current collector made of a nickel foam with a diameter of 18 mm, a thickness of 0.27 mm, and a porosity of 86%, spot welded to the inner surface of the sealing plate, and 4 is a negative electrode current collector made of a nickel foam with a diameter of 17 mm and a thickness of 0.31 m.
A negative electrode active material consisting of a lithium sheet of m is crimped to the current collector 3. 6 has a diameter of 16mm.

厚さ0.15rMlのチタン製エキスパンデッドメタル
からなる正極集電体で、ケース1の内面にスポット溶接
されている。6は正極合剤で、活物iffであるフッ化
炭素を導電材とともにペレット状状に加圧成型した後、
本発明の特徴である定電流放電を実施した後、ケース内
に成型したものである。7はポリプロピレン不織布製セ
パレータである。電解液には、γ−ブチロラクトンと1
,2−ジメトキシエタンとの等量混合溶媒にホウフッ化
リチウムを1モル/lの割合で溶解したものを用いた。
A positive electrode current collector made of expanded titanium metal with a thickness of 0.15 rMl is spot welded to the inner surface of the case 1. 6 is a positive electrode mixture, after press-molding fluorocarbon, which is an active substance IF, into a pellet shape together with a conductive material,
After performing constant current discharge, which is a feature of the present invention, it was molded into a case. 7 is a separator made of polypropylene nonwoven fabric. The electrolyte contains γ-butyrolactone and 1
, 2-dimethoxyethane and lithium borofluoride dissolved at a ratio of 1 mol/l was used.

封1」板に固定した負極集電体およびケースに固定した
正極にそれぞれ電解液を含浸後、七);レ−りの周縁部
をポリプロピレン製絶縁バッキング8の下にまきこんで
封口板とともにカシメ封口して電池を構成した。この電
池は、総高2.5mm、容量160mA hである。
After impregnating the negative electrode current collector fixed to the sealing plate and the positive electrode fixed to the case with the electrolytic solution, 7); Wrap the peripheral edge of the tray under the polypropylene insulating backing 8 and swage it together with the sealing plate. and constructed a battery. This battery has a total height of 2.5 mm and a capacity of 160 mAh.

第3図、第4図に前記従来例電池イと本実施例の電池口
によるものとを比較するために、負荷15KQ、温度2
0℃の初期放電カーブと、負荷16KQ。
3 and 4 show a load of 15 KQ and a temperature of 2 to compare the conventional battery A and the battery port of this embodiment.
Initial discharge curve at 0℃ and load 16KQ.

温度20’C放電の閉路電圧が最低を示す時の、各温度
におけるパルス特性をそれぞれ示す。
The pulse characteristics at each temperature when the closed circuit voltage of discharge at a temperature of 20'C is the lowest are shown.

発明の効果 以上の実施例からも明らかなように、ペレット状に成型
された正極活物質をあらかじめ定電流放電させたものを
使用して構成された電池は、放電初期における閉路電圧
、パルス特性も従来と比較し向上し、かつ製造工程を簡
素化でき、量産性の向上とともに、低コストの電池を得
ることができる。
Effects of the Invention As is clear from the above examples, a battery constructed using a pellet-shaped positive electrode active material that has been subjected to constant current discharge in advance has poor closed-circuit voltage and pulse characteristics at the initial stage of discharge. This is improved compared to the conventional method, the manufacturing process can be simplified, mass productivity can be improved, and a low-cost battery can be obtained.

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

第1図は本発明の実施例における加圧正極合剤の定電流
放電を示す構成略図、第2図は本発明の実施例における
扁平形弁水電解液電池の縦断面図、第3図は放電初期電
圧の比較図、第4図は放電初期における各温度のパルス
特性を示す寵である。 a・・・・・・ペレット秋に成形した正極合剤、3・・
・・負極集電体、4・・・・・・負(りである金属リチ
ウム、5・・・・・正極集電体、6・・・・正極合剤、
FIG. 1 is a schematic configuration diagram showing constant current discharge of a pressurized positive electrode mixture in an embodiment of the present invention, FIG. 2 is a longitudinal cross-sectional view of a flat valve water electrolyte battery in an embodiment of the present invention, and FIG. A comparison diagram of the initial discharge voltage, FIG. 4, is a diagram showing the pulse characteristics at each temperature at the initial stage of discharge. a... Positive electrode mixture formed into pellets, 3...
... Negative electrode current collector, 4... Negative metal lithium, 5... Positive electrode current collector, 6... Positive electrode mixture,
.

Claims (1)

【特許請求の範囲】[Claims] 金属リチウムを負極活物質とし、フッ化炭素を正極活物
質とする非水電解液電池の製造法であって、正極活物質
であるフッ化炭素をペレット状に成型した状態で、あら
かじめ定電流放電を実施した後、玉楼に用いて電池を構
成することを特徴とする非水電解液電池の製造法。
A method of manufacturing a non-aqueous electrolyte battery using metallic lithium as a negative electrode active material and fluorocarbon as a positive electrode active material, in which fluorocarbon, which is the positive electrode active material, is formed into pellets and then subjected to constant current discharge in advance. A method for manufacturing a non-aqueous electrolyte battery, which comprises using it in a gyokurou to form a battery.
JP13122383A 1983-07-18 1983-07-18 Manufacture of nonaqueous electrolytic battery Pending JPS6023957A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13122383A JPS6023957A (en) 1983-07-18 1983-07-18 Manufacture of nonaqueous electrolytic battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13122383A JPS6023957A (en) 1983-07-18 1983-07-18 Manufacture of nonaqueous electrolytic battery

Publications (1)

Publication Number Publication Date
JPS6023957A true JPS6023957A (en) 1985-02-06

Family

ID=15052908

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13122383A Pending JPS6023957A (en) 1983-07-18 1983-07-18 Manufacture of nonaqueous electrolytic battery

Country Status (1)

Country Link
JP (1) JPS6023957A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4948406A (en) * 1986-12-13 1990-08-14 Battelle Memorial Institute Apparatus and process for forming an optical fibre covered by a metallic sleeve

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4948406A (en) * 1986-12-13 1990-08-14 Battelle Memorial Institute Apparatus and process for forming an optical fibre covered by a metallic sleeve

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