GB2313561A - Coating a plate with hydrophobic resin - Google Patents

Coating a plate with hydrophobic resin Download PDF

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Publication number
GB2313561A
GB2313561A GB9708085A GB9708085A GB2313561A GB 2313561 A GB2313561 A GB 2313561A GB 9708085 A GB9708085 A GB 9708085A GB 9708085 A GB9708085 A GB 9708085A GB 2313561 A GB2313561 A GB 2313561A
Authority
GB
United Kingdom
Prior art keywords
plate
hydrophobic
resin
cell
coating
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.)
Withdrawn
Application number
GB9708085A
Other versions
GB9708085D0 (en
Inventor
Su Suk Choi
Jun Hyung Park
Bung Hyun Kang
Jong Wook Lee
Sang Bong Nam
Meen Seon Paik
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.)
Samsung SDI Co Ltd
Original Assignee
Samsung Display Devices 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 Samsung Display Devices Co Ltd filed Critical Samsung Display Devices Co Ltd
Publication of GB9708085D0 publication Critical patent/GB9708085D0/en
Publication of GB2313561A publication Critical patent/GB2313561A/en
Withdrawn legal-status Critical Current

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Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00Secondary cells; Manufacture thereof
    • H01M10/42Methods or arrangements for servicing or maintenance of secondary cells or secondary half-cells
    • H01M10/52Removing gases inside the secondary cell, e.g. by absorption
    • 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
    • H01M4/24Electrodes for alkaline accumulators
    • H01M4/26Processes of manufacture
    • 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
    • H01M4/24Electrodes for alkaline accumulators
    • H01M4/32Nickel oxide or hydroxide electrodes
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00Secondary cells; Manufacture thereof
    • H01M10/34Gastight accumulators
    • H01M10/345Gastight metal hydride accumulators
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10Energy storage using batteries

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Battery Electrode And Active Subsutance (AREA)
  • Cell Separators (AREA)
  • Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)
  • Separation Using Semi-Permeable Membranes (AREA)
  • Fuel Cell (AREA)

Description

2313561 A METHOD OF PREPARING A HYDROPHOBIC PLATE
BACKGROUND OF THE INVENTION
1 Field of the invention
The present invention relates to a method of preparing, a hydrophobic 1 plate, and specifically, to a method of easily preparing a hydrophobic plate having good hydrophobic property by dipping a plate into dispersion solution.
lo 2. Description of the Related Arts
In general a sealed nickel-hydrogen cell that is an alkali storage battery uses metal oxide as an anode and hydrogenated alloy as a cathode. This cell is charged or discharged by storing the hydrogenated alloy hydrogen ions is produced by cleavage of water in the electrolyte during, the charging, process, C1 C) CI and releasing hydrogen ions into the electrolyte during the discharging process. The nickel-hydrogen cell uses hydrogenated alloy as a negative active material, Ni(OH)2 as a positive active material, and alkali aqueous solution as an electrolyte. When the nickel-hydrogen cell is represented by a general formula that is a Ni-MH (nickel-metalhydride) cell Electrical-chemical reactions of the nickel -hydrogen cells are as follows.
2 Anode: NI(OH)2 + OH- N100H + H-20 ----------- (1) Cathode: M + H,0 4--> MH + OH - --------------------- (2) In the above reactions, M is a hydrogenated alloy that can absorb and emit hydrogen ions.
A charge and discharge are performed according to the above reaction, oxygen gas is electrically-chemically generated in the anode during the charge and discharge. When the charge and discharge cycles are continuously performed, the oxygen gas generated causes the cathode to oxidize and the internal pressure of a cell to increase thereby decreasing the capacity of the cell.
lo Accordingly, in order to remove gas by transferring gas generated in the anode to the cathode, hydrophobic property gives to the cathode to extend the interface of the cathode in which cleavage or absorption of gas has occurred.
Fig, 2a shows a negative plate (7) being plated with fluoro-based resin powder as a hydrophobic material by spraying the plate (7) as it is moving in the direction of the arrow (11). Fig. 2b, shows a negative plate (7) being plated with a fluoro-based resin powder as a hydrophobic material by spraying the stationary plate (7) while the spray nozzle (9) is moving, in the direction of the arrow (1 3)). Alcohol that can be readily vaporized after spraying was used w as a medium for spraying, water was not used as a medium because it takes a 1 tp lone, time for water to vaporize thereby oxidizing the plate.
3 As described above, when fluoro resin powder is sprayed on the plate, a three-phase (vapor-liquid-solid) material is formed on the surface of the plate so that gas readily attaches on the plate. Therefore, gas is absorbed or decomposed on the plate so that internal pressure is decreased. However, the s disadvantages of the spray method is that it is difficult to uniformly coat the plate with the fluoro-based resin, and alcohol used as medium is vaporized so that it is harmful to humans and is extremely flammable. Furthermore, the spray method has problems when the hole of the spray nozzle clogs up with the resin of the spray solution, thereby decreasing the operation efficiency.
SUMMARY OF THEE INVENTION
In order to solve the above-mentioned problems of the conventional process, an object of the present invention is to provide a method of preparing is hydrophobic plates, which is not harmful to humans, poses no thereat of causing a fire, and has high operation efficiency.
The secondary object of the present invention Is to provide hydrophobic plates for a cell having low internal pressure and lone, life by using the hydrophobic plate.
While studying a. hydrophobic plate for a cell in order to solve the Z above-mentioned problems, the present inventor discovered that a plate having 1:1 4 good hydrophobic property can be easily prepared, in case of coating a dispersion solution made of hydroFhobic resin. Conventionally, a person havina the ordinary skills in the art thoucht that when a hydrophobic dispersion W is used, it is difficult to prepare a hydrophobic plate, and a plate having bad s hydrophobic property is prepared due to a hydrophilic agent added to promote dispersion, 1. e. interfacial active a ent. Therefore, a method of spraying 9 11.1 powder of a hydrophobic resin on the plate has been used in the conventional process. However, as like the present invention, the plate can be readily coated with hydrophobic resin when a hydrophobic plate is prepared by the io dipping the plate into hydrophobic dispersion solution. Moreover, a cell prepared using the plate has good hydrophobic property, when compared with a cell using a plate prepared by the spray method. Therefore, internal pressure of a cell is decreased, thereby preventing deficiency of an electrolyte in a cell. Furthermore, an electrolyte is uniformly distributed so that a cell having a long life can be prepared.
In order to achieve the object, the present invention provides a method of preparing a hydrophobic plate comprising the steps of coating a plate with a P dispersion solution including hydrophobic resin; and drying said coated plate.
In the present invention, the preferred hydrophobic resin is an aqueous e) to 10 % by weight of a copolymer solution includina fluoro-based resin, U-, - 1:7 of tetrafluoroethylene and hexafluoropropylene, and/or polytetrafluoroethylene.
When dispersion below 3 % by weight of fluoro-based resin is used as a dispersion solution including hydrophobic resin dispersion, a plate having sufficient hydrophobic property can not be produced. Furthermore, when dispersion above 10 % by weight of fluo 0-based is used as a dispersion solution including, hydrophobic resin, the hydrophobic property of a cathode increases. Therefore, it is not preferred to produce a cell using a plate having excess hydrophobic property since the permeation amount of an electrolyte is decreased.
Furthermore, in the present invention, the coatiner step is formed by lo dipping the plate into hydrophobic resin dispersion. It is preferred that the coatina step is carried out for 1 second to 5 minutes in order to obtain 0.2 to 3.0 Mg/CM2 of hydrophobic resin on the plate.
ck In the method of the present invention, it is preferred that b, ck 4 ZCA calendering step is after the drying step because the plate is having uniform thickness can be produced.
Moreover, the method of the present invention can be applied to general molded products as well as a plate of a cell in order to ive good hydrophobic 91 Z1 property.
BRIEF DESCRIPTION OF THE DRAWINGS
6 Fie. 1 (a) is a diagram showing a step of dip-coating a plate into an c C C> aqueous solution including fluoro-based resin to give good hydrophobic 0 1_1.
property to a plate accordina to one embodiment of the present invention; ing a Fit>. 1 (b) is a diagram showing a step of continuously dip-coat' 1-7 plate-roll into an aqueous solution including fluoro-based resin to give good 1 1 C.
hydrophobic property to a plate according to another embodiment of the present invention; Fig. 2 (a) is a diagram showing a step of spraying an aqueous solution lo including fluoro-based resin on plate moving to give hydrophobic property accordina to the conventional method; and Fig. 2 (b) is a diagram showing a step of spraying an aqueous solution includina fluoro-based resin on a plate with a spray nozzle moving accordine, to the conventional method.
is DETAILED DESCRIPTION OF THE INVENTION
The present invention is further explained in more detail with reference to the following example which is within the scope of this invention.
[Example 1]
A cathode of a nickel-hydrogen cell was dipped into 5 wt% of a 7 copolymer of tetra fl uoroethyl ene and hexafluoropropylene, ND-1 (1, Japan, Dikyn Co. Ltd.) for 5 sec. as shown in Fig. 1 (a), and dried in an oven at 601C.
The thickness of the dried plate is controlled by calendering with roller to prepare a hydrophobic plate.
[Example 2]
A hydrophobic plate was prepared by the same procedure as in Example 1 except that a dispersion solution including polytetrafluoroethylene, LDW-40 0 (1, Japan, Takedayakuhing Co, Ltd.) was used as a dispersion solution including fluoro-based resin instead of ND-1, and plate-roll (5) is continuously lo dipped into the dispersion as shown in Fig. 1 (b).
[Comparative example 1] Fluoro-based resin powder is sprayed on a plate while the plate (7) was moving (11) as shown in Fig. 2 (a) to prepare a hydrophobic plate.
[Comparative example 2] is Fluoro-based resin powder is sprayed on a plate while a spray'nozzle (9) was moving (13) as shown in Fig. 2 (b) to prepare a hydrophobic plate.
After the cells were prepared using hydrophobic plate obtained according to the above example and comparative example, the cells were char ed and discharged for 100 times, internal pressure and lifetime (ICY. 9 90% level of total capacity) of these cells were determined and the results thereof is shown in the followina table 1.
W 8 I. Table 1
Internal pressure Lifetime [atmospheric pressure] (When the cell was charged 1 and discharaed once) Z_ [CY] Example 1 5 3 50 Example 2 6
Comparative 20 250 Example 1
Comparative 20 250 Example 2
Conventionally, a person having ordinary skills in the art thought that when hydrophobic dispersion is used, it is difficult to prepare a hydrophobic -5 plate, and a plate having bad hydrophobic property is prepared due to hydrophilic agent added to promote dispersion, i. e. interfacial active agent. Therefore, a method of spraying powder of hydrophobic resin on the plate has been used in the conventional process. However, as like the present invention, the plate can be readily coated with tiydrophobic resin when a hydrophobic lo plate was prepared by dipping the plate into hydrophobic dispersion solution. Moreover, a cell prepared using, the plate has good hydrophobic property, when 9 compared with a cell using a plate prepared by a spray method. Therefore, internal pressure of a cell is decreased, thereby preventing deficiency of an electrolyte in a cell. Furthermore, an electrolyte is uniformly distributed so that a cell having a long life can be prepared.
As shown in the above table 1, the method of coating dispersion solution of the present invention can be effectively performed, when compared with the method of spraying powder. Furthermore, dust is not scattered thereby easily preparing a hydrophobic plate, and an amount of fluoro- based resin coated on a plate is easily controlled by controlling the concentration of io the dispersion aqueous solution.
The method of preparing hydrophobic plate of the present invention can be applied to a method of preparing plates for various fields, such as a condenser as well as a cell in preparing a plate with the object of increasing C1 contact area of a gas.
Moreover, the method of the present invention is a useful method to give hydrophobic property to certain objects.

Claims (10)

CLAIMS:
1. A method of preparing a hydrophobic plate comprising the steps of:
coating a plate with a dispersion solution including hydrophobic resin; and drying said coated plate.
2. A method of preparing a hydrophobic molded product comprising the steps of:
coating a molded product with dispersion solution including hydrophobic resin; and drying said coated molded product.
3. A method according to claim 1 or claim 2, wherein the dispersion solution is an aqueous solution including 3 to 10 wt'i of hydrophobic resin.
4. A method according to any one of claims 1 to 3, wherein the hydrophobic resin is a fluoro-based resin.
5. A method according to claim 4, wherein the fluoro based resin comprises a copolymer of tetrafluoroethylene and hexafluoropropylene, and/or polytetrafluoroethylene.
6. A method according to any one of claims 1 to 5, wherein the coating is performed by dipping the plate into the dispersion solution.
7. A method according to claim 6, wherein the dipping is maintained until 0.2 to 3.0 Mg/CM2 of the hydrophobic resin is coated on the plate.
8. A method according to claim 6 or claim 7, wherein the dipping is performed for 1 second to 5 minutes.
9. A method according to any one of claims 1 to 8, further comprising a calendering step to uniform the thickness of the coated plate or molded product af ter the drying step.
10. A hydrophobic plate or a hydrophobic molded product produced by a method according to any one of claims 1 to 9.
GB9708085A 1996-05-31 1997-04-22 Coating a plate with hydrophobic resin Withdrawn GB2313561A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
KR1019960019135A KR0172229B1 (en) 1996-05-31 1996-05-31 Method of manufacturing hydrophobic plate

Publications (2)

Publication Number Publication Date
GB9708085D0 GB9708085D0 (en) 1997-06-11
GB2313561A true GB2313561A (en) 1997-12-03

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ID=19460386

Family Applications (1)

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GB9708085A Withdrawn GB2313561A (en) 1996-05-31 1997-04-22 Coating a plate with hydrophobic resin

Country Status (11)

Country Link
JP (1) JPH1040905A (en)
KR (1) KR0172229B1 (en)
CN (1) CN1170247A (en)
DE (1) DE19716704A1 (en)
ES (1) ES2125832B1 (en)
FR (1) FR2749195A1 (en)
GB (1) GB2313561A (en)
IT (1) IT1291648B1 (en)
NL (1) NL1006184C2 (en)
SE (1) SE9701907L (en)
SG (1) SG71706A1 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999033126A1 (en) * 1997-12-19 1999-07-01 Wang Jin San Metal-hydride hydrogen storage rechargeable batteries
US9023556B2 (en) 2006-03-17 2015-05-05 GM Global Technology Operations LLC Method of preparing gas diffusion media for a fuel cell

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5975307B2 (en) * 2012-11-28 2016-08-23 パナソニックIpマネジメント株式会社 Nickel metal hydride storage battery and battery pack

Citations (8)

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Publication number Priority date Publication date Assignee Title
JPS5214749B2 (en) * 1972-12-22 1977-04-23
JPS5372139A (en) * 1976-12-09 1978-06-27 Matsushita Electric Ind Co Ltd Method of manufacturing positive electrode plate for alkaline storage battery
WO1982003802A1 (en) * 1981-04-28 1982-11-11 Shamrock Corp Diamond Method of depositing cation exchange membrane on a foraminous cathode
US4503099A (en) * 1983-06-15 1985-03-05 Borg-Warner Corporation Heat transfer surfaces having scale resistant polymer coatings thereon
JPH01143141A (en) * 1987-11-27 1989-06-05 Shin Kobe Electric Mach Co Ltd Manufacture of electrode
JPH0660876A (en) * 1992-08-12 1994-03-04 Nippon Oil Co Ltd Alkaline storage battery and manufacture thereof
JPH0660871A (en) * 1992-08-07 1994-03-04 Nippon Oil Co Ltd Zinc negative electrode for alkaline battery and manufacture thereof
US5514495A (en) * 1993-08-11 1996-05-07 Varta Batterie Aktiengesellschaft Negative electrode for gastight alkaline storage batteries having a carbon-black-containing gas-consumption layer

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JPS5112643A (en) * 1974-07-19 1976-01-31 Matsushita Electric Ind Co Ltd Denchokyokubanno seizoho
FR2513906A1 (en) * 1981-10-06 1983-04-08 Morin Joel Coating metal surface with antistick or anti:lubricating compsn. - comprising mixt. of PTFE and thermoplastic fluorinated resin
US5034289A (en) * 1989-02-23 1991-07-23 Matsushita Electric Industrial Co., Ltd. Alkaline storage battery and method of producing negative electrode thereof
JPH02227966A (en) * 1989-02-28 1990-09-11 Matsushita Electric Ind Co Ltd Sealed alkaline storage battery and manufacture of its negative electrode
JP2918560B2 (en) * 1989-03-09 1999-07-12 古河電池株式会社 Manufacturing method of hydrogen storage electrode
US5242765A (en) * 1992-06-23 1993-09-07 Luz Electric Fuel Israel Limited Gas diffusion electrodes
JPH07240200A (en) * 1994-02-28 1995-09-12 Fuji Photo Film Co Ltd Nonaqueous secondary battery

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5214749B2 (en) * 1972-12-22 1977-04-23
JPS5372139A (en) * 1976-12-09 1978-06-27 Matsushita Electric Ind Co Ltd Method of manufacturing positive electrode plate for alkaline storage battery
WO1982003802A1 (en) * 1981-04-28 1982-11-11 Shamrock Corp Diamond Method of depositing cation exchange membrane on a foraminous cathode
US4503099A (en) * 1983-06-15 1985-03-05 Borg-Warner Corporation Heat transfer surfaces having scale resistant polymer coatings thereon
JPH01143141A (en) * 1987-11-27 1989-06-05 Shin Kobe Electric Mach Co Ltd Manufacture of electrode
JPH0660871A (en) * 1992-08-07 1994-03-04 Nippon Oil Co Ltd Zinc negative electrode for alkaline battery and manufacture thereof
JPH0660876A (en) * 1992-08-12 1994-03-04 Nippon Oil Co Ltd Alkaline storage battery and manufacture thereof
US5514495A (en) * 1993-08-11 1996-05-07 Varta Batterie Aktiengesellschaft Negative electrode for gastight alkaline storage batteries having a carbon-black-containing gas-consumption layer

Non-Patent Citations (5)

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Title
JAPIO Abstract 89094/E815/13/396/pp116 & JP 01 143 141 A *
JAPIO Abstract 940602/E1557/18/290/pp65 & JP 06 060 876 A *
JAPIO Abstract 940602/E557/18/290/pp64 & JP 06 060 871 A *
WPI Abstract Acc. No 78-43321A/24 & JP 52 014 749 B *
WPI Abstract Acc. No 78-55848A/31 & JP 53 072 139 A *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999033126A1 (en) * 1997-12-19 1999-07-01 Wang Jin San Metal-hydride hydrogen storage rechargeable batteries
US9023556B2 (en) 2006-03-17 2015-05-05 GM Global Technology Operations LLC Method of preparing gas diffusion media for a fuel cell

Also Published As

Publication number Publication date
NL1006184A1 (en) 1997-12-03
SG71706A1 (en) 2000-04-18
ES2125832A1 (en) 1999-03-01
JPH1040905A (en) 1998-02-13
IT1291648B1 (en) 1999-01-19
ITMI970955A0 (en) 1997-04-24
KR0172229B1 (en) 1999-03-30
DE19716704A1 (en) 1997-12-04
CN1170247A (en) 1998-01-14
SE9701907L (en) 1997-12-01
ES2125832B1 (en) 1999-11-16
KR970077787A (en) 1997-12-12
FR2749195A1 (en) 1997-12-05
NL1006184C2 (en) 1999-06-08
SE9701907D0 (en) 1997-05-22
ITMI970955A1 (en) 1998-10-24
GB9708085D0 (en) 1997-06-11

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