JPS63257181A - Manufacture of positive plate for cylinder type lithium battery - Google Patents
Manufacture of positive plate for cylinder type lithium batteryInfo
- Publication number
- JPS63257181A JPS63257181A JP9020187A JP9020187A JPS63257181A JP S63257181 A JPS63257181 A JP S63257181A JP 9020187 A JP9020187 A JP 9020187A JP 9020187 A JP9020187 A JP 9020187A JP S63257181 A JPS63257181 A JP S63257181A
- Authority
- JP
- Japan
- Prior art keywords
- positive plate
- positive electrode
- electrode plate
- roller
- plate
- 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
- 238000004519 manufacturing process Methods 0.000 title claims description 10
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 title claims description 6
- 229910052744 lithium Inorganic materials 0.000 title claims description 6
- 229910052751 metal Inorganic materials 0.000 claims description 7
- 239000002184 metal Substances 0.000 claims description 7
- 239000007774 positive electrode material Substances 0.000 claims description 6
- 239000006258 conductive agent Substances 0.000 claims description 2
- 239000011230 binding agent Substances 0.000 claims 1
- 238000003825 pressing Methods 0.000 abstract description 5
- 239000008151 electrolyte solution Substances 0.000 abstract description 3
- 238000000034 method Methods 0.000 abstract description 3
- 230000003247 decreasing effect Effects 0.000 abstract 2
- 239000011149 active material Substances 0.000 abstract 1
- 239000003792 electrolyte Substances 0.000 description 14
- 238000010248 power generation Methods 0.000 description 6
- 230000007423 decrease Effects 0.000 description 5
- 238000010521 absorption reaction Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- FBDMJGHBCPNRGF-UHFFFAOYSA-M [OH-].[Li+].[O-2].[Mn+2] Chemical compound [OH-].[Li+].[O-2].[Mn+2] FBDMJGHBCPNRGF-UHFFFAOYSA-M 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 101150093156 Rras gene Proteins 0.000 description 1
- 239000006230 acetylene black Substances 0.000 description 1
- 239000002313 adhesive film Substances 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- TXEYQDLBPFQVAA-UHFFFAOYSA-N tetrafluoromethane Chemical compound FC(F)(F)F TXEYQDLBPFQVAA-UHFFFAOYSA-N 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
- H01M4/08—Processes of manufacture
-
- 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
- H01M4/04—Processes of manufacture in general
-
- 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
- H01M4/04—Processes of manufacture in general
- H01M4/0402—Methods of deposition of the material
- H01M4/0404—Methods of deposition of the material by coating on electrode collectors
-
- 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
- H01M4/04—Processes of manufacture in general
- H01M4/043—Processes of manufacture in general involving compressing or compaction
- H01M4/0435—Rolling or calendering
Landscapes
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Battery Electrode And Active Subsutance (AREA)
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明は円筒形リテレム電池の正極板の製造法に関する
。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a method for manufacturing a positive electrode plate for a cylindrical lithium battery.
従来の技術
一般に、円筒形リチウム電池の正極は、主として二酸化
マンガンもしくはフッ化炭素よりなる正極活物質にアセ
チレンブラック等導電剤を加え、さらにバ春ンダー及び
水を加えて混練し、その後金属製集電網の片面もしくは
両面に前記混線物(以下ペーストと称する)を付着して
形成されている。ついで金属製集電網に付着されたペー
スト(以下正極板と称する)は、乾燥後ローラによって
加圧される。電池の放電容量を高めるべく、ペースト量
を大として加圧すれば、正極活物質充填量が大きくなる
が、以下のような問題点が発生していた。Conventional technology In general, the positive electrode of a cylindrical lithium battery is made by adding a conductive agent such as acetylene black to a positive electrode active material mainly made of manganese dioxide or carbon fluoride, and then kneading the mixture with balunder and water. It is formed by adhering the interfering material (hereinafter referred to as paste) to one or both sides of the electric grid. The paste (hereinafter referred to as a positive electrode plate) attached to the metal current collection net is then dried and then pressed by a roller. In order to increase the discharge capacity of the battery, increasing the amount of paste and applying pressure increases the amount of positive electrode active material filled, but the following problems have occurred.
発明が解決しようとする問題点
(1) ローラ加圧時正極板にひずみが生じ、第2図
に示すような正極板3の変形が発生する。電池はこの付
着膜よりなる正極とリチウムよりなる負極と番セパレー
タを介して渦巻状に巻回し、発電群を構成し、これを有
底筒状の金属缶に挿入して電解液を注液し、その後封口
して製造される。正極板が変形した場合、発電群構成が
困難となり電池内部短絡を発生する場合があった。Problems to be Solved by the Invention (1) When the roller presses the positive electrode plate, the positive electrode plate is strained, and the positive electrode plate 3 is deformed as shown in FIG. The battery consists of a positive electrode made of this adhesive film, a negative electrode made of lithium, and a separator, which are wound in a spiral shape to form a power generation group, which is then inserted into a bottomed cylindrical metal can and filled with electrolyte. , and then sealed and manufactured. If the positive electrode plate was deformed, it would be difficult to configure a power generation group, and short circuits within the battery could occur.
僻)正極板内部の空孔率が減少し、正極板の電解液保液
能力が低下する。したがって、電解液注液後、発電群が
電解液を吸収するまでに時間がかかり、電池組立上大き
な時間的損失となっていた。偻) The porosity inside the positive electrode plate decreases, and the electrolyte retention capacity of the positive electrode plate decreases. Therefore, after the electrolyte is injected, it takes time for the power generation group to absorb the electrolyte, resulting in a large time loss in battery assembly.
また、発電群が電解液を充分に吸収しない間に電池が封
口される場合があり、その場合封日時電解液が電池外部
に漏液し電池内の電解液量が不足して電池の放電容量が
低下するという問題があった。In addition, the battery may be sealed while the power generation group does not absorb enough electrolyte, and in that case, the electrolyte leaks to the outside of the battery and the amount of electrolyte in the battery becomes insufficient, resulting in the battery's discharge capacity. There was a problem that the
本発明は、以上のような問題点を解決するもので、円筒
形リチウム電池の正極板を製造するにあたり、正極板の
変形が少なく従って発電群構成が容易で、電解液の吸液
性に優れた正極板を得ることを目的とする。The present invention solves the above-mentioned problems, and when manufacturing a positive electrode plate for a cylindrical lithium battery, there is little deformation of the positive electrode plate, so the power generation group configuration is easy, and the electrolyte absorption property is excellent. The purpose is to obtain a positive electrode plate.
問題点を解決するための手段
本発明は、正極活物質を含むペーストを金属製集電網の
片面もしくは両面に膜状に付着して正極板を形成し、つ
いで前記正極板を乾燥後ローラに通して加圧し、さらに
その後前記正極板を前記加圧ローラ径の6〜10%の径
に少なくとも1回以上わん曲して正極板密度をローラ加
圧直後の正極板密度に比して0.3〜6%低下させるも
のである。Means for Solving the Problems The present invention involves depositing a paste containing a positive electrode active material in the form of a film on one or both sides of a metal current collector net to form a positive electrode plate, and then passing the positive electrode plate through a roller after drying. After that, the positive electrode plate is bent at least once to a diameter of 6 to 10% of the pressure roller diameter, so that the positive electrode plate density is 0.3 compared to the positive electrode plate density immediately after being pressed by the roller. ~6% reduction.
作 用
本発明による製造法によれば、正極板は、ローラ加圧後
のわん曲てより、ローラ加圧時て発生する正極板内部ひ
ずみが減少し、電池放電容量を高めるべくペースト量を
増加してもローラ加圧後に発生する正極板の変形を低減
することができる。Function: According to the manufacturing method of the present invention, the positive electrode plate is bent after being pressed by the roller, so that the internal strain of the positive electrode plate that occurs when the roller is pressed is reduced, and the amount of paste is increased to increase the battery discharge capacity. However, deformation of the positive electrode plate that occurs after roller pressure can be reduced.
また、本発明によれば、ローラ加圧後に密度が高められ
、空孔率が減少させられた正極板を、ローラ加圧後の正
極板わん曲により、特に正極板表面における空孔率を増
加することが可能である。従って本発明によれば、変形
が少なく発電群構成が容易で、かつ電解液保液効果の良
好な正極板を得ることができる。Further, according to the present invention, the porosity of the positive electrode plate, which has been increased in density and reduced in porosity after roller pressure is applied, is increased by curving the positive electrode plate after roller pressure is applied, particularly on the surface of the positive electrode plate. It is possible to do so. Therefore, according to the present invention, it is possible to obtain a positive electrode plate that is less deformed, is easy to configure as a power generation group, and has a good electrolyte retaining effect.
実施例
第1図イは正極活物質を含むペーストを金属製集電網に
付着し、さらに乾燥された正極板3の加圧ローラによる
加圧及び、加圧後のわん曲を示す図である。図において
、1は加圧ローラ、2は正極板わん曲ローラを示す。本
実施例では、ローラ加圧後の正極板わん曲を加圧ローラ
直径に比して10%の直径を有する6本のローラにより
行った。Embodiment FIG. 1A is a diagram showing the application of a paste containing a positive electrode active material to a metal current collector net, and the pressing of a dried positive electrode plate 3 with a pressure roller and the curvature after the pressing. In the figure, 1 indicates a pressure roller, and 2 indicates a positive electrode plate curved roller. In this example, the positive electrode plate was bent after being pressed by a roller using six rollers each having a diameter that was 10% of the diameter of the pressure roller.
一定の曲率にわん曲が可能であれば、本実施例のように
ローラによるわん曲を用いる必要はなく、例えば第1図
口に示すように一定の曲率を有する曲板4に正極板3を
通過させても良い。またわん曲の径は加圧ローラの径に
比較して、40%以上であれば、正極板のわん曲による
密度低下は見られないが、正極板内部のひずみを十分に
取り除くことも不可能であり、ローラ加圧による正極板
変形を減少することは困難であった。また、わん曲の径
が小さい場合、金属製集電網に付着したペーストに脱落
が生じることがあり、正極板のローラ加圧後のわん曲の
径は、加圧ローラ径に比較して5%〜40%が適当であ
る。このようにして得られる正極板の密度は、わん曲に
より、ローラ加圧直後に比較して0.3〜゛6%低下す
るが、この密度低下は、主にわん曲の外周部すなわち正
極板の表面部分に顕著に表われることが顕微鏡観察によ
り明らかであり、この正極板表面部分を中心とした密度
低下が正極板吸液性の向上に寄与するものと考えられる
。If it is possible to curve the plate to a constant curvature, there is no need to use a roller to curve it as in this embodiment. For example, as shown in the opening in FIG. You can let it pass. Also, if the diameter of the curvature is 40% or more compared to the diameter of the pressure roller, there will be no density reduction due to the curvature of the positive electrode plate, but it will also be impossible to sufficiently remove the strain inside the positive electrode plate. Therefore, it was difficult to reduce the deformation of the positive electrode plate due to roller pressure. In addition, if the diameter of the curve is small, the paste attached to the metal current collection net may fall off, and the diameter of the curve after the positive electrode plate is pressed by the roller is 5% compared to the diameter of the pressure roller. ~40% is appropriate. The density of the positive electrode plate obtained in this way decreases by 0.3 to 6% due to the curvature compared to immediately after roller pressure is applied, but this decrease in density mainly occurs at the outer periphery of the curvature, that is, the positive electrode plate It is clear from microscopic observation that the density is clearly visible on the surface area of the positive electrode plate, and it is thought that this decrease in density centered on the positive electrode plate surface area contributes to the improvement of the positive electrode plate liquid absorption property.
表1に円筒形二酸化マンガンリチウム電池の正極板にお
いて本発明を実施した例を示す。Table 1 shows examples in which the present invention was implemented in positive electrode plates for cylindrical lithium manganese dioxide batteries.
なお、表中の電解液吸液時間は、幅20 rras 、
長さ200w+厚さ0.4ranの寸法に正極板を切り
出し、電解液1.0yをスポイトにて、正極板の中央部
に滴下して、電解液が、正極板中に浸透するまでに要し
た時間である。In addition, the electrolyte liquid absorption time in the table is width 20 rras,
A positive electrode plate was cut into a size of 200W in length + 0.4ran in thickness, and 1.0y of electrolyte was dropped into the center of the positive plate using a dropper.The time required for the electrolyte to penetrate into the positive plate was It's time.
また、本実施例では6本のローラにより正極板を6回わ
ん曲したが、1回わん曲でも上記のような実施効果が得
られる。しかしながら2回〜5図のわん曲において本発
明の最も有効な実施効果が得られた。Further, in this example, the positive electrode plate was bent six times by six rollers, but the above-mentioned effects can be obtained even if the positive electrode plate is bent once. However, the most effective implementation effect of the present invention was obtained in the curves shown in Figures 2 to 5.
なお、わん曲を6回以上行った場合、正極活物質が金属
製集電網より脱落する場合があった。In addition, when the curve was performed six times or more, the positive electrode active material sometimes fell off from the metal current collection net.
本発明を円筒形二酸化マンガンリチウム電池CR2/3
A(直径17朋、高さ33.6mm)において実施し、
本発明の製造法による電池Iと、従来の製造法による電
池■との比較結果を表2に示した。なお、組立て電池数
は各n = 30で実施した。表中の放電サイクル数は
、9oomAの電流にて3秒放電し、その後27秒休止
する30秒1サイクルのパルス放電を20℃の温度下に
て個い、電池電圧が1.55V を維持する間の放電
サイクル数を示す。The present invention is a cylindrical manganese dioxide lithium battery CR2/3
Conducted at A (diameter 17 mm, height 33.6 mm),
Table 2 shows the comparison results between Battery I manufactured by the manufacturing method of the present invention and Battery ■ manufactured by the conventional manufacturing method. The number of assembled batteries was n = 30. The number of discharge cycles in the table is to discharge at a current of 9oomA for 3 seconds, then pause for 27 seconds, then pulse discharge for 1 cycle of 30 seconds at a temperature of 20℃, and maintain the battery voltage at 1.55V. Indicates the number of discharge cycles between.
なお本実施例ておける正極板密度は、ローラムロ圧直後
2.95〜3.0グ/c c であり、わん向後は2
.9〜2.95y/CCであった。また、正極板を電解
液に20秒浸漬した場合の正極板の電解液吸液量は本発
明による正極板は1.2 ccに対し、従来の正極板の
場合09ccであった。In addition, the positive electrode plate density in this example was 2.95 to 3.0 g/cc immediately after roller roller pressure, and 2.95 to 3.0 g/cc after one-way pressure.
.. It was 9-2.95y/CC. Further, when the positive electrode plate was immersed in the electrolytic solution for 20 seconds, the amount of electrolyte absorbed by the positive electrode plate was 1.2 cc for the positive electrode plate according to the present invention, whereas it was 09 cc for the conventional positive electrode plate.
発明の効果
上述より明らかなように、本発明の製造法によれば、電
池組立が容易で、電解液吸液能力の優れた正極板を得る
ことができ、よって、電池性能の向上をはかることがで
きる。Effects of the Invention As is clear from the above, according to the manufacturing method of the present invention, it is possible to easily assemble a battery and obtain a positive electrode plate with excellent electrolyte absorption ability, thereby improving battery performance. Can be done.
第1図イ2口は本発明の正極板製造法を示す工程図、第
2図は従来の製造法による正極板外観図である。
1・・・・・・加圧ローラ、2・・・・・わん曲ローラ
、3・・・・・・正極板、4・・・・・・曲板。Figure 1A2 is a process diagram showing the positive electrode plate manufacturing method of the present invention, and Figure 2 is an external view of the positive electrode plate according to the conventional manufacturing method. 1... Pressure roller, 2... Curved roller, 3... Positive electrode plate, 4... Curved plate.
Claims (1)
金属製集電網に膜状に付着して極板を形成し、ついで前
記極板を乾燥した後にローラに通して加圧し、しかる後
に、前記極板を前記加圧ローラ径の5%〜10%の径に
少なくとも1回以上わん曲し、極板のペースト密度をロ
ーラ加圧直後のペースト密度に比較して0.3〜5%低
下させることを特徴とする円筒形リチウム電池正極板の
製造法。A paste consisting of a positive electrode active material, a conductive agent, and a binder is adhered in a film form to a metal current collection net to form an electrode plate, and then the electrode plate is dried and then passed through a roller and pressurized. is bent at least once to a diameter of 5% to 10% of the pressure roller diameter to reduce the paste density of the electrode plate by 0.3 to 5% compared to the paste density immediately after roller pressure. A manufacturing method for the characteristic cylindrical lithium battery positive electrode plate.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9020187A JPS63257181A (en) | 1987-04-13 | 1987-04-13 | Manufacture of positive plate for cylinder type lithium battery |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9020187A JPS63257181A (en) | 1987-04-13 | 1987-04-13 | Manufacture of positive plate for cylinder type lithium battery |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS63257181A true JPS63257181A (en) | 1988-10-25 |
Family
ID=13991873
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP9020187A Pending JPS63257181A (en) | 1987-04-13 | 1987-04-13 | Manufacture of positive plate for cylinder type lithium battery |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63257181A (en) |
-
1987
- 1987-04-13 JP JP9020187A patent/JPS63257181A/en active Pending
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