JPH01283764A - Lithium cell - Google Patents
Lithium cellInfo
- Publication number
- JPH01283764A JPH01283764A JP11391788A JP11391788A JPH01283764A JP H01283764 A JPH01283764 A JP H01283764A JP 11391788 A JP11391788 A JP 11391788A JP 11391788 A JP11391788 A JP 11391788A JP H01283764 A JPH01283764 A JP H01283764A
- Authority
- JP
- Japan
- Prior art keywords
- positive electrode
- pellets
- binder
- powder
- improved
- 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
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 title claims description 4
- 229910052744 lithium Inorganic materials 0.000 title claims description 4
- 239000000843 powder Substances 0.000 claims abstract description 11
- 239000000835 fiber Substances 0.000 claims abstract description 10
- 239000011230 binding agent Substances 0.000 claims abstract description 9
- 239000000203 mixture Substances 0.000 claims description 15
- 229910052751 metal Inorganic materials 0.000 claims description 5
- 239000002184 metal Substances 0.000 claims description 5
- 239000007774 positive electrode material Substances 0.000 claims description 5
- 239000008188 pellet Substances 0.000 abstract description 20
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract description 5
- 239000003792 electrolyte Substances 0.000 abstract description 5
- 238000010521 absorption reaction Methods 0.000 abstract description 4
- 230000015572 biosynthetic process Effects 0.000 abstract description 2
- 239000006185 dispersion Substances 0.000 abstract description 2
- 239000002131 composite material Substances 0.000 abstract 3
- 239000013543 active substance Substances 0.000 abstract 2
- 229920000914 Metallic fiber Polymers 0.000 abstract 1
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 238000000465 moulding Methods 0.000 description 5
- 239000005486 organic electrolyte Substances 0.000 description 5
- 238000007789 sealing Methods 0.000 description 4
- 229920006367 Neoflon Polymers 0.000 description 3
- KLARSDUHONHPRF-UHFFFAOYSA-N [Li].[Mn] Chemical compound [Li].[Mn] KLARSDUHONHPRF-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 2
- -1 polytetrafluoroethylene Polymers 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 1
- PYVHTIWHNXTVPF-UHFFFAOYSA-N F.F.F.F.C=C Chemical compound F.F.F.F.C=C PYVHTIWHNXTVPF-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- MHCFAGZWMAWTNR-UHFFFAOYSA-M lithium perchlorate Chemical compound [Li+].[O-]Cl(=O)(=O)=O MHCFAGZWMAWTNR-UHFFFAOYSA-M 0.000 description 1
- 229910001486 lithium perchlorate Inorganic materials 0.000 description 1
- 239000011812 mixed powder Substances 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920005606 polypropylene copolymer Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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
- H01M4/06—Electrodes for primary cells
-
- 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
- H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
- H01M4/624—Electric conductive fillers
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明は有機電解液電池であるリチウム電池の正極合剤
に関するものである。DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to a positive electrode mixture for a lithium battery, which is an organic electrolyte battery.
従来の技術
有機電解液電池の正極は、従来正極活物質粉末と導電性
炭素粉末の混合粉末にデイスパージョン形の結着剤を加
えて混練し、この混合合剤を乾燥、整粒後、加圧成形し
ペレットとすることを実施していたが、このようにして
作成する正極合剤ペレットは結着剤を多量に混入しない
とペレット強度が得られず、結着剤の少ない場合はペレ
ットの成型が困難となり、成型ができた場合でも強度不
足の為、電池組立時の搬送工程の衝撃でペレットの周縁
のカケ、ヒビ割れが生じる問題があった。Conventional technology The positive electrode of an organic electrolyte battery is conventionally made by adding a dispersion-type binder to a mixed powder of positive electrode active material powder and conductive carbon powder and kneading the mixture.After drying and sizing this mixture, Previously, the positive electrode mixture pellets created in this way had to be mixed with a large amount of binder to obtain pellet strength. It becomes difficult to mold the pellets, and even if molding is possible, the lack of strength causes chips and cracks at the edges of the pellets due to impact during the transportation process during battery assembly.
また、ペレット強度を向上させるために、従来よシよく
使用されているポリ4弗化エチレン、4弗化エチレンと
6弗化プロピレンの共重合体(商品名:ネオフロン)等
を多く混入するとペレット強度は向上するが、ペレット
の電解液吸液性が悪くなり、正極活物質の放電利用率が
悪いと言う問題があった。In addition, in order to improve the pellet strength, adding a large amount of polytetrafluoroethylene, a copolymer of tetrafluoroethylene and hexafluoropropylene (trade name: NEOFLON), etc., which has been commonly used in the past, will strengthen the pellet. However, there was a problem in that the electrolyte absorption properties of the pellets deteriorated and the discharge utilization rate of the positive electrode active material was poor.
発明が解決しようとする課題
本発明は、有機電解液電池の正極のペレット強度の問題
を結着剤の増量を伴なわずして解決することを目的とす
るものである。Problems to be Solved by the Invention The present invention aims to solve the problem of the pellet strength of the positive electrode of an organic electrolyte battery without increasing the amount of binder.
課題を解決するための手段
この問題を解決するために本発明は、正極活物質粉末と
導電性炭素粉末に直径6〜60μm、長さ1〜6ffの
金属繊維を混合し、その後ダイスバージョン形の結着剤
を加えて正極合剤としたものである。Means for Solving the Problems In order to solve this problem, the present invention mixes metal fibers with a diameter of 6 to 60 μm and a length of 1 to 6 ff with positive electrode active material powder and conductive carbon powder, and then mixes them into a dice version. A binder was added to form a positive electrode mixture.
作用
本発明は、絡み性の良好な金属短繊維を正極合剤中に均
一に分散させているため、加圧成形時のペレット強度が
向上し、割れ、かけ等も極めて少なくできる。Function In the present invention, short metal fibers with good entanglement properties are uniformly dispersed in the positive electrode mixture, so that the pellet strength during pressure molding is improved and cracking, chipping, etc. can be extremely reduced.
また、この方法は結着剤量を従来の約捧に減らすことが
可能であり、ペレットの電解液吸液性が向上する結果、
この正極ペレットを使用する電池の放電特性も向上する
ことが明らかとなった。In addition, this method allows the amount of binder to be reduced to about the same level as conventional methods, and as a result, the electrolyte absorption ability of the pellets improves.
It has become clear that the discharge characteristics of batteries using this positive electrode pellet are also improved.
実施例 以下本発明の詳細な説明する。Example The present invention will be explained in detail below.
焼成二酸化マンガン粉末97重量部と、導電性炭素質粉
末としてケッチエンブラック3重量部との混合割合で攪
拌した合剤1000gに、ステンレス鋼5us430の
短繊維、直径30μm、長さ3囮を50gと6弗化プロ
ピレンと4弗化エチレンの共重合体(ネオフロン)のデ
ィスバージ、ヨン41gと純水460111を加え、攪
拌混練する。To 1000 g of a mixed mixture of 97 parts by weight of calcined manganese dioxide powder and 3 parts by weight of Ketchen Black as a conductive carbonaceous powder, 50 g of short fibers of stainless steel 5us430, diameter 30 μm, length 3 decoys were added. Add 41 g of Disverge, a copolymer of propylene hexafluoride and ethylene tetrafluoride (Neoflon), and 460111 g of pure water, and stir and knead.
この湿潤合剤を120℃の熱風で乾燥し、水分を除去し
た後、32メツシユの金網で整粒し顆粒状合剤を得る。This wet mixture was dried with hot air at 120° C. to remove moisture, and then sized with a 32-mesh wire mesh to obtain a granular mixture.
この顆粒状合剤をプレス成形機によって、重量0.35
g 、直径16龍、厚さ0.72 mlKのペレット
に加圧成形して有機電解液電池の正極を得る。This granular mixture was molded using a press molding machine with a weight of 0.35
A positive electrode for an organic electrolyte battery was obtained by pressure molding into a pellet with a diameter of 16 mm and a thickness of 0.72 mlK.
上記実施例の記載には、8 u 8430の短繊維を示
したが、アルミニウム、チタン、5uS444などの短
繊維も本発明の実施例と同等の効果を生じる。In the description of the above examples, short fibers of 8u8430 are shown, but short fibers of aluminum, titanium, 5uS444, etc. also produce the same effect as the examples of the present invention.
第1図は本発明のリチウムマンガン電池の縦断面図を示
すもので、1はステンレス鋼5uS430よりなる正極
缶、2は5u1430よりなる封口板、3は実施例によ
って得られた正極4は封口板2の内面に圧着固定された
リチウム負極、6は合成繊維不織布からなるセパレータ
、6はポリプロピレンのガスケットでこのガスケットを
介して正極缶1と封口板2とを圧接密閉した有機電解液
電池である。電解液はプロピレンカーボネットとジメト
キシエタンの混合液に過塩素酸リチウムを溶解したもの
を用いた。FIG. 1 shows a longitudinal cross-sectional view of the lithium manganese battery of the present invention, in which 1 is a positive electrode can made of stainless steel 5uS430, 2 is a sealing plate made of 5u1430, and 3 is a positive electrode 4 obtained in the example is a sealing plate. A lithium negative electrode is press-fixed to the inner surface of 2, a separator 6 is made of synthetic fiber non-woven fabric, and 6 is a polypropylene gasket, and the cathode can 1 and the sealing plate 2 are press-fitted and sealed via this gasket.This is an organic electrolyte battery. The electrolyte used was a mixture of propylene carbonate and dimethoxyethane in which lithium perchlorate was dissolved.
第1表は、本発明によるペレット状正極ムと従来法とし
て焼成二酸化マンガンとアクシカ−ボン−との合剤にネ
オ70ンデイスバージヨンを上記実施例と同じ混合量使
用し、同一工程で製造した従来のペレット状正JfMB
を加圧成形する時の1000個当シの不良数と成形ペレ
ットを200 ’Cで12時間熱風乾燥後、組立工程の
搬送過程で発先した割れ数を1000個当シで比較した
ものである。Table 1 shows the results of the pelletized positive electrode according to the present invention and the conventional method in which Neo 70-day version was used in a mixture of calcined manganese dioxide and Axica carbon in the same mixing amount as in the above example, and manufactured in the same process. Conventional pellet-shaped positive JfMB
This is a comparison of the number of defects per 1,000 pieces when press-molding the molded pellets and the number of cracks that started during the conveyance process of the assembly process after drying the molded pellets with hot air at 200'C for 12 hours. .
第1表
第2図は本発明による正極ムと従来の正極Bを使用した
同型のリチウムマンガン電池の1xΩの定抵抗負荷によ
る連続放電性能を比較したものである。第2図より明ら
かなごとく放電性能は本発明の正極ムを使用したものが
若干良い。この放電性能の差は正極の電解液の吸収性と
金属短繊維の電子電導ネットワーク形成の相乗効果によ
り二酸化マンガンの利用率が向上したものと考えられる
。Table 1 and FIG. 2 compare the continuous discharge performance under a constant resistance load of 1xΩ of the same type of lithium manganese battery using the positive electrode according to the present invention and the conventional positive electrode B. As is clear from FIG. 2, the discharge performance using the positive electrode of the present invention is slightly better. This difference in discharge performance is thought to be due to the improved utilization of manganese dioxide due to the synergistic effect of the electrolyte absorption of the positive electrode and the formation of an electronic conductive network of the short metal fibers.
発明の効果
以上の様に、正極物質粉末と導電性炭素微粉末と金属短
繊維とネオフロンデイスパージョンとを攪拌混合し、乾
燥後整粒した合剤を加圧成形してペレット状正極とする
ことによシ、合剤の強度が増大し、組立の搬送工程にお
ける衝撃にも強く、ペレットが割れたシ、周縁部が欠け
る等の問題がなぐなシ、工業的価値は大きい。As described above, the positive electrode material powder, conductive carbon fine powder, short metal fibers, and neoflon dispersion are stirred and mixed, dried, and the sized mixture is pressure-molded to form a pellet-like positive electrode. By doing so, the strength of the mixture is increased, it is resistant to impact during the transportation process of assembly, and problems such as pellet cracking and chipping of the periphery are avoided, which is of great industrial value.
第1図は本発明によって得られた正極を備えたである。
1・・・・・・正極缶、2・・・・・・封口板、3・・
・・・・正極、4・・・・・・負i、s・・・・・・セ
パレータ、6・・・・・・ガスケット。FIG. 1 shows a cathode provided with a positive electrode obtained according to the present invention. 1...Positive electrode can, 2...Sealing plate, 3...
... Positive electrode, 4... Negative i, s... Separator, 6... Gasket.
Claims (1)
維と結着剤とから構成されているリチウム電池。A lithium battery in which the positive electrode mixture is composed of positive active material powder, conductive fine powder, short metal fibers, and a binder.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11391788A JPH01283764A (en) | 1988-05-11 | 1988-05-11 | Lithium cell |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11391788A JPH01283764A (en) | 1988-05-11 | 1988-05-11 | Lithium cell |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01283764A true JPH01283764A (en) | 1989-11-15 |
Family
ID=14624427
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11391788A Pending JPH01283764A (en) | 1988-05-11 | 1988-05-11 | Lithium cell |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01283764A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6338920B1 (en) * | 1997-02-04 | 2002-01-15 | Mitsubishi Denki Kabushiki Kaisha | Electrode for lithium ion secondary battery and lithium ion secondary battery using the same |
-
1988
- 1988-05-11 JP JP11391788A patent/JPH01283764A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6338920B1 (en) * | 1997-02-04 | 2002-01-15 | Mitsubishi Denki Kabushiki Kaisha | Electrode for lithium ion secondary battery and lithium ion secondary battery using the same |
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