WO2003028129A1 - Alkali dry cell - Google Patents
Alkali dry cell Download PDFInfo
- Publication number
- WO2003028129A1 WO2003028129A1 PCT/JP2002/008898 JP0208898W WO03028129A1 WO 2003028129 A1 WO2003028129 A1 WO 2003028129A1 JP 0208898 W JP0208898 W JP 0208898W WO 03028129 A1 WO03028129 A1 WO 03028129A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- positive electrode
- weight
- manganese dioxide
- load discharge
- parts
- Prior art date
Links
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M6/00—Primary cells; Manufacture thereof
- H01M6/04—Cells with aqueous electrolyte
- H01M6/06—Dry cells, i.e. cells wherein the electrolyte is rendered non-fluid
- H01M6/08—Dry cells, i.e. cells wherein the electrolyte is rendered non-fluid with cup-shaped electrodes
- H01M6/085—Dry cells, i.e. cells wherein the electrolyte is rendered non-fluid with cup-shaped electrodes of the reversed type, i.e. anode in the centre
-
- 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
- H01M4/36—Selection of substances as active materials, active masses, active liquids
- H01M4/362—Composites
- H01M4/364—Composites as mixtures
-
- 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
- H01M4/36—Selection of substances as active materials, active masses, active liquids
- H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
- H01M4/50—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese
-
- 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
- H01M4/36—Selection of substances as active materials, active masses, active liquids
- H01M4/58—Selection of substances as active materials, active masses, active liquids of inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFy; of polyanionic structures, e.g. phosphates, silicates or borates
- H01M4/5825—Oxygenated metallic salts or polyanionic structures, e.g. borates, phosphates, silicates, olivines
-
- 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
-
- 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
- H01M4/625—Carbon or graphite
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M6/00—Primary cells; Manufacture thereof
- H01M6/04—Cells with aqueous electrolyte
- H01M6/06—Dry cells, i.e. cells wherein the electrolyte is rendered non-fluid
- H01M6/08—Dry cells, i.e. cells wherein the electrolyte is rendered non-fluid with cup-shaped electrodes
-
- 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
- H01M2004/026—Electrodes composed of, or comprising, active material characterised by the polarity
- H01M2004/028—Positive electrodes
-
- 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
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
Definitions
- the present invention relates to an alkaline battery. Background art
- anatase-type titanium oxide for example, Japanese Patent Application Laid-Open No. 8-510355
- titanium oxide are mainly used as positive electrode additives in order to improve the heavy load discharge characteristics.
- Composite oxides for example, Japanese Patent Application Laid-Open No. 9-139201
- barrier compounds such as barrier sulfate.
- the present invention is an alkaline dry battery comprising a positive electrode, a negative electrode, and an alkaline electrolyte, wherein the positive electrode comprises manganese dioxide and graphite powder, and
- T i and (S 0 4) relates to an alkaline dry battery comprising as an additive.
- T i (S 0 4) 2 the amount included in the positive electrode, per the manganese dioxide 1 0 0 parts by weight, 0. It is preferable from 1 to 5 parts by weight.
- FIG. 1 is a partial vertical sectional view of an example of an alkaline dry battery according to the present invention.
- the positive electrode of the alkaline dry battery of the present invention comprises manganese dioxide as a positive electrode active material, graphite powder as a conductive material, and titanium sulfate as an additive.
- the effect of increasing the utilization rate of the positive electrode active material in heavy load discharge or medium load discharge can be expected.
- the moldability of the positive electrode is improved and the active material filling amount is increased, an effect of suppressing a decrease in light load discharge characteristics can be expected.
- the reason for the decrease in the utilization rate of the positive electrode active material during heavy load discharge or medium load discharge is considered to be that the crystal lattice of manganese dioxide is deformed during discharge and the conductivity of the positive electrode is degraded.
- the positive electrode of the alkaline dry battery of the present invention contains T i (SO 4) 2 , sulfate ions are generated inside the positive electrode.
- This sulfate ion is considered to enter the space of the crystal lattice of manganese dioxide and suppress the deformation of the crystal lattice during discharge. Therefore, the crystal lattice maintains the initial state even at the end of discharge It is thought that the movement and diffusion of protons that govern the reduction reaction of the positive electrode are smooth, and that the conductivity of the positive electrode can be prevented from deteriorating.
- T i (S 0 4) 2 is water soluble.
- T i (S 0 4) 2 aqueous solution, can and Hatasuko also serves as a binder of the positive electrode mixture composed of manganese dioxide and a conductive material. That is, the T i (S 0 4) 2 , to improve the moldability of the positive electrode mixture, the effect of increasing the filling amount to the battery of the positive electrode can be expected.
- T i (so 4 ) 2 exerts an effect equal to or greater than that of a conventional additive even in a small amount. Therefore, an effect of increasing the active material filling amount in the positive electrode, that is, an effect of suppressing deterioration of light load discharge performance, can be expected as compared with the related art.
- T i (SO 4) 2 can exert the same or better effect even in a small amount is considered to be that the ionization degree is large and it is possible to supply more sulfate ions.
- the positive electrode 1 0 0 parts by weight per manganese dioxide, 0.5 1. ⁇ 5 parts by weight of T i (S 0 4) preferably contains 2. If the amount of T i (S 0 4) 2 is more than 5 parts by weight, there tends to decrease the light load discharge characteristics, at the 1 part by weight less than 0.5, heavy load discharge characteristics and Z or middle load discharge characteristics It will be difficult to improve this sufficiently.
- the amount of T i (S ⁇ 4 ) 2 is particularly preferably 1 to 3 parts by weight per 100 parts by weight of manganese dioxide.
- T i (SO 4) 2 is used as it is as a powder, the powder has high hygroscopicity, which makes it difficult to control the amount added in the production process.
- T i (S 0 4) 2 is preferably added to the positive electrode mixture as an aqueous solution.
- the concentration of T i (S ⁇ 4 ) 2 in the aqueous solution is less than 1% by weight,
- the amount of the aqueous solution containing the T i (S 0 4) 2 is increased, the moldability of the positive electrode mixture is low down.
- the positive electrode mixture for example, manganese dioxide and graphite powder are mixed at a predetermined ratio. Mixing, the resulting mixture was added to T i (S 0 4) 2 aqueous solution, by further mixing, can be prepared.
- the obtained positive electrode mixture is usually compression-molded into flakes. The flake-shaped positive electrode mixture is then pulverized into granules and classified by sieving. Then, a positive electrode mixture composed of particles having a size of 10 to 100 mesh is pressure-formed into a short cylindrical pellet.
- manganese dioxide and graphite powder those conventionally used can be used without any particular limitation.
- the negative electrode and the alkaline electrolyte those conventionally used can be used without any particular limitation.
- FIG. 1 shows a partial vertical cross-sectional view of an alkaline dry battery manufactured in an example of the present invention.
- a battery case 1 the inside of a battery case 1 is filled with a plurality of positive electrode mixtures 2 formed into a short cylindrical pellet in a state of being in close contact with the inner wall of the case.
- a gelled negative electrode 3 is accommodated in the hollow portion of the positive electrode mixture 2 via a cylindrical separator 4 having a bottom.
- the battery case 1 a case made of steel with nickel plating on the inner surface or the like can be used.
- Separe Night 4 there is a bottom paper 9 for reinforcement.
- the base paper 9 is made of the same material as the separator 4.
- This battery was manufactured as follows.
- T i (S 0 4) which is adjusted to a predetermined concentration 2 aqueous solution was added additive, and mixed.
- the amount of aqueous solution used herein, the amount of T i (S_ ⁇ 4) 2, 1 0 0 parts by weight per manganese dioxide was adjusted to a predetermined amount shown in Table 1 (X parts by weight).
- a cylindrical separator 4 with a bottom was placed in the hollow portion of the positive electrode mixture 2 placed inside the battery case 1.
- a predetermined amount of alkaline electrolyte was injected into Separation 4 and absorbed into Separation 4 for a predetermined time.
- the gelled negative electrode 3 was filled into the Separation overnight 4.
- the negative electrode current collector 6 was inserted into the center of the gelled negative electrode 3.
- the negative electrode current collector 6 used was integrated with the gasket 5 and the bottom plate 7 also serving as the negative electrode terminal.
- the gelled negative electrode 3 was prepared by mixing 33 parts by weight of an alkaline electrolyte, 1 part by weight of a gelling agent, and 66 parts by weight of zinc powder. Sodium polyacrylate was used as the gelling agent.
- As the alkaline electrolyte a 40% by weight aqueous hydroxide aqueous solution was used.
- a non-woven fabric made of polyvinyl alcohol fiber and rayon fiber was used as the separator 4 and the base paper 9.
- the obtained dry battery was evaluated as follows.
- the initial (immediately after production) alkaline batteries were continuously discharged at a load of 2.2 ⁇ and a cut-off voltage of 0.9 V, and the discharge time was measured.
- the result of the alkaline dry battery (Comparative Example 1) to which T i (S C) 2 was not added was set to 100, which is a reference value, and the heavy load discharge characteristics were expressed as an index. Table 1 shows the results.
- the medium-load discharge characteristics were evaluated in the same manner as the above-mentioned heavy-load discharge characteristics, except that continuous discharge was performed with a load of 10 ⁇ .
- the light-load discharge characteristics were evaluated in the same manner as the above-mentioned heavy-load discharge characteristics, except that continuous discharge was performed with a load of 39 ⁇ . Table 1 also shows these results.
- Table 1 shows that when the amount of Ti (SCU) 2 added to the positive electrode mixture is 0.1 to 5 parts by weight per 100 parts by weight of manganese dioxide, the heavy-load discharge characteristics of the alkaline dry battery can be improved. Excellent and no deterioration in light load discharge characteristics I understand that On the other hand, T i (S 0 4) 2 quantities Gilt be small as in Example 1, et whether the effect of improving the positive electrode active material utilization ratio is not obtained very much, the heavy load discharge characteristics are hardly improved I understand. Also,
- T i (S 0 4) 2 T i ⁇ 2 except for using (Comparative Example 2) or B a SO 4 (Comparative Example 3) was manufactured create the same alkaline dry battery of Example 3. That is, in Comparative Example 2, 1 part by weight of Ti 2 per 100 parts by weight of manganese dioxide was used, and in Comparative Example 3, 1 part by weight of BaSO 4 was used per 100 parts by weight of manganese dioxide. Was.
- an alkaline dry battery which is excellent in heavy load discharge characteristics and medium load discharge characteristics and in which a decrease in light load discharge characteristics is suppressed.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Inorganic Chemistry (AREA)
- Composite Materials (AREA)
- Crystallography & Structural Chemistry (AREA)
- Primary Cells (AREA)
- Battery Electrode And Active Subsutance (AREA)
Description
Claims
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR10-2004-7003901A KR20040040464A (ko) | 2001-09-25 | 2002-09-02 | 알칼리 건전지 |
CA002459503A CA2459503A1 (en) | 2001-09-25 | 2002-09-02 | Alkali dry cell |
BR0212351-7A BR0212351A (pt) | 2001-09-25 | 2002-09-02 | Bateria alcalina seca |
US10/487,342 US7326496B2 (en) | 2001-09-25 | 2002-09-02 | Alkali dry cell |
AU2002328409A AU2002328409B2 (en) | 2001-09-25 | 2002-09-02 | Alkali dry cell |
EP02762972A EP1432057A4 (en) | 2001-09-25 | 2002-09-02 | ALKALINE DRY CELL |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2001291385A JP4137417B2 (ja) | 2001-09-25 | 2001-09-25 | アルカリ乾電池 |
JP2001-291385 | 2001-09-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2003028129A1 true WO2003028129A1 (en) | 2003-04-03 |
Family
ID=19113536
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2002/008898 WO2003028129A1 (en) | 2001-09-25 | 2002-09-02 | Alkali dry cell |
Country Status (9)
Country | Link |
---|---|
US (1) | US7326496B2 (ja) |
EP (1) | EP1432057A4 (ja) |
JP (1) | JP4137417B2 (ja) |
KR (1) | KR20040040464A (ja) |
CN (1) | CN1240153C (ja) |
AU (1) | AU2002328409B2 (ja) |
BR (1) | BR0212351A (ja) |
CA (1) | CA2459503A1 (ja) |
WO (1) | WO2003028129A1 (ja) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20130029210A1 (en) * | 2010-03-02 | 2013-01-31 | Satoshi Minoura | Lead acid storage battery |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2000024071A1 (en) * | 1998-10-21 | 2000-04-27 | Duracell Inc. | Titanium additives for manganese dioxide cathode electrochemical cell |
WO2000030198A1 (en) * | 1998-11-13 | 2000-05-25 | Eveready Battery Company, Inc. | Electrochemical cell having electrode additives |
JP2001297776A (ja) * | 2000-04-13 | 2001-10-26 | Sony Corp | アルカリ電池 |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3337568A1 (de) | 1983-10-15 | 1985-04-25 | Varta Batterie Ag, 3000 Hannover | Herstellung von elektrolytischem braunstein fuer alkalische zellen |
JPS63126165A (ja) * | 1986-11-17 | 1988-05-30 | Matsushita Electric Ind Co Ltd | 非水電解液二次電池用正極活物質の製造法 |
US5342712A (en) | 1993-05-17 | 1994-08-30 | Duracell Inc. | Additives for primary electrochemical cells having manganese dioxide cathodes |
US5569564A (en) | 1995-06-07 | 1996-10-29 | Eveready Battery Company, Inc. | Alkaline cell having a cathode including a titanate additive |
DE19532073C2 (de) * | 1995-08-31 | 2000-02-24 | Univ Dresden Tech | Verfahren zur Herstellung von modifiziertem Braunstein für Batterie-Elektroden |
US5744266A (en) | 1996-02-02 | 1998-04-28 | Matsushita Electric Industrial Co., Ltd. | Batteries and a method of manufacturing positive active material for the batteries |
US5733674A (en) * | 1997-02-12 | 1998-03-31 | Law; Steven | Power supply systems for portable electronic devices |
JPH10308217A (ja) | 1997-03-06 | 1998-11-17 | Matsushita Electric Ind Co Ltd | アルカリ乾電池 |
US6387123B1 (en) * | 1999-10-13 | 2002-05-14 | Advanced Cardiovascular Systems, Inc. | Stent with radiopaque core |
US6585881B2 (en) * | 2001-02-20 | 2003-07-01 | The Gillette Company | Process for manufacture and improved manganese dioxide for electrochemical cells |
-
2001
- 2001-09-25 JP JP2001291385A patent/JP4137417B2/ja not_active Expired - Fee Related
-
2002
- 2002-09-02 KR KR10-2004-7003901A patent/KR20040040464A/ko active IP Right Grant
- 2002-09-02 BR BR0212351-7A patent/BR0212351A/pt not_active Application Discontinuation
- 2002-09-02 CA CA002459503A patent/CA2459503A1/en not_active Abandoned
- 2002-09-02 WO PCT/JP2002/008898 patent/WO2003028129A1/ja active IP Right Grant
- 2002-09-02 EP EP02762972A patent/EP1432057A4/en not_active Withdrawn
- 2002-09-02 CN CNB028184882A patent/CN1240153C/zh not_active Expired - Fee Related
- 2002-09-02 AU AU2002328409A patent/AU2002328409B2/en not_active Ceased
- 2002-09-02 US US10/487,342 patent/US7326496B2/en not_active Expired - Fee Related
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2000024071A1 (en) * | 1998-10-21 | 2000-04-27 | Duracell Inc. | Titanium additives for manganese dioxide cathode electrochemical cell |
WO2000030198A1 (en) * | 1998-11-13 | 2000-05-25 | Eveready Battery Company, Inc. | Electrochemical cell having electrode additives |
JP2001297776A (ja) * | 2000-04-13 | 2001-10-26 | Sony Corp | アルカリ電池 |
Non-Patent Citations (1)
Title |
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See also references of EP1432057A4 * |
Also Published As
Publication number | Publication date |
---|---|
EP1432057A4 (en) | 2007-06-20 |
CA2459503A1 (en) | 2003-04-03 |
CN1557032A (zh) | 2004-12-22 |
CN1240153C (zh) | 2006-02-01 |
BR0212351A (pt) | 2004-07-27 |
US7326496B2 (en) | 2008-02-05 |
KR20040040464A (ko) | 2004-05-12 |
JP2003100297A (ja) | 2003-04-04 |
EP1432057A1 (en) | 2004-06-23 |
AU2002328409B2 (en) | 2005-04-21 |
JP4137417B2 (ja) | 2008-08-20 |
US20040209167A1 (en) | 2004-10-21 |
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