US20040191613A1 - Method and apparatus for manufacturing battery electrode plate and battery using the same - Google Patents
Method and apparatus for manufacturing battery electrode plate and battery using the same Download PDFInfo
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- US20040191613A1 US20040191613A1 US10/823,863 US82386304A US2004191613A1 US 20040191613 A1 US20040191613 A1 US 20040191613A1 US 82386304 A US82386304 A US 82386304A US 2004191613 A1 US2004191613 A1 US 2004191613A1
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- 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
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/04—Construction or manufacture in general
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/24—Alkaline accumulators
- H01M10/28—Construction or manufacture
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/24—Alkaline accumulators
- H01M10/30—Nickel accumulators
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/34—Gastight accumulators
- H01M10/345—Gastight metal hydride accumulators
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- 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
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- 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
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- 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
- H01M4/0416—Methods of deposition of the material involving impregnation with a solution, dispersion, paste or dry powder
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- 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
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- 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
- H01M4/24—Electrodes for alkaline accumulators
- H01M4/26—Processes of manufacture
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- 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
- H01M4/64—Carriers or collectors
- H01M4/70—Carriers or collectors characterised by shape or form
- H01M4/80—Porous plates, e.g. sintered carriers
- H01M4/808—Foamed, spongy materials
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- 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
- H01M6/10—Dry cells, i.e. cells wherein the electrolyte is rendered non-fluid with wound or folded electrodes
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- 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
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- 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
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
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- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T29/00—Metal working
- Y10T29/49—Method of mechanical manufacture
- Y10T29/49002—Electrical device making
- Y10T29/49108—Electric battery cell making
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- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T29/00—Metal working
- Y10T29/49—Method of mechanical manufacture
- Y10T29/49002—Electrical device making
- Y10T29/49108—Electric battery cell making
- Y10T29/49115—Electric battery cell making including coating or impregnating
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- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T29/00—Metal working
- Y10T29/49—Method of mechanical manufacture
- Y10T29/4998—Combined manufacture including applying or shaping of fluent material
- Y10T29/49982—Coating
Definitions
- the present invention relates to a battery electrode plate used in a rechargeable battery such as a nickel metal hydride battery or a nickel cadmium battery, and more particularly to a method and apparatus for manufacturing a non-sintered battery electrode plate including a foamed metal core substrate impregnated with an active material, and a battery using such a battery electrode plate.
- the core substrate 1 is impregnated with an active material 3 , the active material 3 accumulated inside the slots 2 is removed using a brush or the like. Subsequently, in a second pressing process, the core substrate 1 is subjected to three press working steps and converted to a form shown in FIG. 7C in which the entire surface is level with the bottom of the slots 2 . The sections where the slots 2 had been formed are then subjected to an active material removal process using a brush and an air blower to form core substrate exposed sections 4 as shown in FIG. 7D. The core substrate 1 is then cut, forming battery electrode plates 7 .
- a current collector 7 b including the core substrate exposed section 4 is formed on one edge of the battery electrode plate 7 , and a cylindrical electrode group formed by winding this electrode plate has a current collector on one end surface. Because this electrode group collects current uniformly along the entire length of the battery electrode plate, the current collecting efficiency improves. In addition, by employing a tab-less method wherein a current collecting lead plate is welded to the aforementioned current collector, the current collection characteristics improve markedly, enabling the demands for improvements in high rate discharge characteristics to be met.
- a first problem is that because variations in the impregnation density of the active material 3 occur within active material impregnated sections 7 a, there is a variation in the capacity of batteries produced using these battery electrode plates 7 , and so when applied to a battery pack, there is an increased likelihood of over charging or over discharging.
- a second problem is that because a boundary line 7 c between the active material impregnated section 7 a and the current collector 7 b is not a true straight line, the precision of the dimensions and shape of the battery electrode plate 7 is low, leading to a reduction in the current collecting function of a battery produced using this battery electrode plate 7 , and a failure to achieve high rate discharge characteristics.
- a third problem is that because the removal of the active material 3 from the current collector 7 b is imperfect, there is an increased likelihood of unsatisfactory welding occurring during attachment of the current collecting lead plate to the current collector 7 b, resulting in a reduced yield. Removal of the active material using a brush and air blower is also inefficient, and invites a reduction in productivity.
- a fourth problem is that the width of the core substrate exposed sections 4 shown in FIG. 7D, prior to cutting, differs from the preset value. As a result, a method wherein the core substrate exposed section is folded at right angles and then compressed to form the current collector cannot be applied, and so it becomes impossible to ensure the mechanical strength of the current collector or a high current collection efficiency.
- a fifth problem is that the battery electrode plates 7 obtained by cutting the core substrate 1 are susceptible to warping into a bow shape.
- this warping can be the cause of weaving, resulting in an electrode group of an unsatisfactory shape.
- fine cracks also develop at the boundary section between the active material impregnated section 7 a and the current collector 7 b, and sections of the metallic skeleton of the core substrate 1 rupture, leading to a deterioration in strength.
- this type of battery electrode plate 7 is susceptible to problems such as dropout of the active material 3 , short circuiting, and deterioration in the electrical conductivity.
- Japanese Laid-Open Patent Publication No. 2000-77054 discloses another method of manufacturing a battery electrode plate. This method involves impregnating an entire core substrate composed of a foamed metal with an active material, subsequently carrying out press working to compress the entire core substrate to a predetermined thickness, and then forming core substrate exposed sections by removing the active material from certain regions using an ultrasonic vibration device.
- the present invention takes the conventional problems described above into consideration, with an object of providing a method and apparatus for manufacturing a battery electrode plate in which there is no variation in the impregnation density of the active material, the boundary line between the active material impregnated sections and the current collector is a true straight line, the residual ratio of the active material in the current collector is low, and the entire current collector has a predetermined width, as well as providing a battery which utilizes such a battery electrode plate.
- a method for manufacturing a battery electrode plate according to the present invention includes an active material impregnation step for impregnating an entire porous core substrate shaped like a thin plate with an active material; a pressing step for performing press working on the active material impregnated core substrate to form a plurality of rail shaped protrusions; an active material removal step for removing the active material to form core substrate exposed sections by applying ultrasonic vibrations to the rail shaped protrusions; a flattening step for pressing down on the top of the core substrate exposed sections and compressing the exposed sections down to the same level as the other sections; and a cutting step for cutting predetermined sections including the core substrate exposed sections to form individual battery electrode plates.
- An electrode group produced by spirally winding the battery electrode plates of a positive and negative electrode produced by the above method, with a separator interposed therebetween, can be placed within a cylindrical battery case to form a cylindrical battery.
- Another method for manufacturing a battery electrode plate according to the invention includes an active material impregnation step for impregnating an entire porous core substrate shaped like a thin plate with an active material; a pressing step for performing press working on the active material impregnated core substrate to form a plurality of rail shaped protrusions; an active material removal step for removing the active material to form core substrate exposed sections by applying ultrasonic vibrations to the rail shaped protrusions; a core substrate exposed section compression step for compressing the core substrate exposed sections; a lead welding step for seam welding a lead hoop to the core substrate exposed sections; and a cutting step for cutting predetermined sections including the lead hoop to form individual battery electrode plates.
- An electrode group produced by alternately laminating the battery electrode plates of a positive and negative electrode produced by the above method, with a separator interposed therebetween, can be placed within a prismatic battery case to form a prismatic battery.
- An apparatus for manufacturing a battery electrode plate of the present invention includes a stripe roller press device for performing press working on an active material impregnated core substrate formed from a porous core substrate shaped like a thin plate, to form a plurality of rail shaped protrusions; and an active material removal device including an ultrasonic vibration device for bringing an ultrasound generation horn into contact with the rail shaped protrusions and applying ultrasonic vibrations and a vacuum suction device positioned in an opposing position below each ultrasonic vibration device for suctioning the active material removed by the application of ultrasonic vibrations.
- Another apparatus for manufacturing a battery electrode plate of the invention includes a stripe roller press device for performing press working on an active material impregnated core substrate formed from a porous core substrate shaped like a thin plate, to form a plurality of rail shaped protrusions; an active material removal device including an ultrasonic vibration device for bringing an ultrasound generation horn into contact with the rail shaped protrusions and applying ultrasonic vibrations and a vacuum suction device positioned in an opposing position below each ultrasonic vibration device for suctioning the active material removed by the application of ultrasonic vibrations; a welding device for seam welding a lead hoop to a core substrate exposed sections formed by the active material removal device; and a cutter for cutting predetermined sections including the lead hoop to form individual battery electrode plates.
- FIG. 1A, FIG. 1B, FIG. 1C, FIG. 1D, FIG. 1E and FIG. 1F are perspective views showing the sequence of production steps in a method for manufacturing a battery electrode plate according to a first embodiment of the present invention
- FIG. 2A is a front view showing a stripe roller press device used in a pressing step of the above method, and FIG. 2B is an enlarged view of the portion IIB of FIG. 2A;
- FIG. 3A is a front view showing an active material removal device used in an active material removal step
- FIG. 3B is a right hand side view of the removal device
- FIG. 4 is a partially cutaway perspective view showing a cylindrical battery containing a battery electrode plate produced by the above method
- FIG. 5A, FIG. 5B, FIG. 5C, FIG. 5D, FIG. 5E, FIG. 5F and FIG. 5G are perspective views showing the sequence of production steps in a method for manufacturing a battery electrode plate according to a second embodiment of the invention.
- FIG. 6 is a partially cutaway perspective view of a prismatic battery containing a battery electrode plate produced by the above method.
- FIG. 7A, FIG. 7B, FIG. 7C, FIG. 7D and FIG. 7E are perspective views showing the sequence of production steps in a conventional method for manufacturing a battery electrode plate.
- FIG. 1A through FIG. 1F are perspective views showing the sequence of production steps in a method for manufacturing a battery electrode plate according to a first embodiment of the invention.
- the active material 3 is impregnated into the totally flat core substrate 1 prior to press working, and so is impregnated with a uniform density throughout the entire core substrate 1 , and moreover because the surface of the core substrate 1 is not irregular, namely there are no elevation differences, the active material 3 is retained within the substrate without flowing, and consequently dries with the uniform impregnation density maintained.
- the core substrate 1 is a foamed nickel metal with a three dimensional network structure, and is formed as a rectangular thin sheet with a thickness of 1.24 mm, for example.
- the manufacturing method of this embodiment should preferably be applied to a continuous strip type core substrate, namely a hoop core substrate.
- the entire surface of the core substrate 1 with the exception of those sections which form core substrate exposed sections 13 in subsequent steps, is subjected to press working, and the thickness of the substrate is compressed to approximately half, from the aforementioned 1.24 mm, down to 0.6 mm for example.
- two parallel rail shaped protrusions 8 , 8 with a thickness of approximately 0.9 mm to 1.1 mm are formed.
- a stripe roller press device 9 such as that shown in FIG. 2A is used for this press working.
- FIG. 2A is a front view of the stripe roller press device 9
- FIG. 2B is an enlarged view of the portion IIB of FIG. 2A
- the stripe roller press device 9 includes a supporting press roller 10 and a working press roller 11 , wherein the supporting press roller 10 is supported at a fixed position but is free to rotate, and the working press roller 11 is subjected to a predetermined pressure toward the press roller 10 .
- the working press roller 11 possesses a rigidity capable of withstanding the applied pressure, and is provide with annular slots 12 , 12 at two predetermined positions around the circumference of the roller for forming the protrusions 8 , 8 .
- the opening rim sections of the two side walls 12 a, 12 b of the annular slots 12 are curved surfaces with a radius of curvature R of 0.3 mm to 0.6 mm, for example.
- the two press rollers 10 , 11 have comparatively large roller diameters of 550 mm for example, and in the pressing step of this embodiment, the active material impregnated core substrate 1 which passes between the two press rollers 10 , 11 is worked from the state shown in FIG. 1B to the state shown in FIG. 1C in a single press working step in which a comparatively large pressure of 300 ton, for example, is applied.
- the pitch of the two rail shaped protrusions 8 , 8 thus formed is determined by the dimensions of the annular slots 12 , and conforms precisely to the preset value.
- a conventional method for manufacturing a battery electrode plate includes two pressing steps
- only one pressing step is needed for forming the two protrusions 8 , 8 , and so elongation and deformation of the core substrate is suppressed, although the single pressing step must be able to ensure the predetermined thickness and the predetermined impregnation density of the active material 3 described above.
- experimental results revealed that 3 ton of load was necessary per 1 cm width of electrode plate.
- the gap between the two press rollers 10 , 11 should preferably be widened and set at a value of 0.3 mm for example, and in such a case, an applied pressure of 10 ton/cm is required.
- the second pressing step of the conventional manufacturing method pressing is performed three times using a relatively small press roller with a diameter of 400 mm, and produces a lengthwise elongation of as much as 6%. This elongation is the cause of the bow shaped warping which occurs when the core substrate 1 is divided into individual battery electrode plates 7 .
- the lengthwise elongation is restricted to a value between 1.7% and 1.9% as described above, and when the core substrate 1 is divided into individual battery electrode plates 19 in a subsequent step, almost no warping or cracking occurs.
- the opening rim sections of the two side walls 12 a, 12 b of the annular slots 12 formed in the working press roller 11 are curved surfaces with a radius of curvature R of 0.3 mm to 0.6 mm, the boundaries between the protrusions 8 , 8 and the surrounding regions is clearly defined, and moreover rupture or deterioration of the metal skeleton of the core substrate 1 does not occur during the press working.
- the radius of curvature R of the curved surfaces is set to a value greater than the range from 0.3 mm to 0.6 mm, the active material 3 of the edge of the protrusions 8 , 8 may drop out and the boundaries between the protrusions 8 , 8 and the surrounding regions becomes indistinct, whereas if the radius of curvature R is smaller than the aforementioned range, there is a danger of rupture or deterioration of the metal skeleton of the core substrate 1 , and a battery produced using such a battery electrode plate would display a reduced current collecting efficiency.
- FIG. 1D the active material 3 impregnated within the two protrusions 8 , 8 is removed, forming two rail shaped core substrate exposed sections 13 , 13 .
- FIG. 3A and FIG. 3B show an active material removal device 14 used in this step, wherein FIG. 3A is a front view and FIG. 3B is a right hand side view.
- the active material removal device 14 includes a pair of ultrasonic vibration devices 17 , 17 for stripping away and removing active material 3 by bringing ultrasound generation horns 17 a, 17 a into contact with the tops of the protrusions 8 , 8 and applying ultrasonic vibrations, and a pair of vacuum suction devices 18 , 18 positioned in an opposing position below each of the ultrasonic vibration devices 17 , 17 for suctioning active material 3 which has been stripped away and removed.
- the ultrasound generation horns 17 a have a sloped surface 17 b, with a downhill pitch in the direction of the movement of the core substrate 1 , at the contact surface with the core substrate 1 , and this sloped surface 17 b prevents damage to the core substrate 1 . Furthermore, in order to reduce abrasion, the sloped surface 17 b, and a flat contact surface 17 c which is a continuation of the sloped surface 17 b, are formed using sintered carbides, and the main body of the ultrasound generation horn 17 a is formed from titanium.
- the core substrate 1 is moved in the direction of the arrow shown in FIG. 3B, with the tops of the protrusions 8 , 8 held in contact with the ultrasound generation horns 17 a of the pair of positionally fixed ultrasonic vibration devices 17 , 17 .
- the metal skeleton is squeezed and the active material 3 contained therein is stripped away and removed, while at the same time, the vacuum suction device 18 suctions out and removes active material 3 impregnated within the protrusion 8 and the region below the protrusion.
- the active material 3 contained within the protrusion 8 and the region therebelow is almost entirely removed, yielding a high quality core substrate exposed section 13 .
- the active material 3 to be removed in the aforementioned active material removal step is the active material impregnated within the protrusion 8 , and because the protrusion 8 has not been subjected to press working, the active material 3 is extremely easy to remove. Consequently, even in the case of active material 3 which contains a binder, which has proved extremely difficult to remove using conventional methods, by applying ultrasonic vibration to the substrate by bringing the ultrasound generation horn 17 a of the ultrasonic vibration device 17 into contact with the substrate while applying suction from below with the vacuum suction device 18 , the active material 3 is removed easily and completely.
- the active material residual ratio of a core substrate exposed section 13 formed through the aforementioned active material removal step is from 1 to 4%.
- the active material residual ratio of a core substrate exposed section 4 formed in the conventional manufacturing method is much higher, at 10% or more, and furthermore lumps of active material 3 still exist, and these lumps are the main cause of spark generation during the welding of the current collecting lead plates. Accordingly, these lumps are removed by hand, which leads to a further reduction in productivity.
- Evaluation of the active material residual ratios described above was conducted by immersion into an aqueous solution of acetic acid, which dissolves only the active material 3 without dissolving the nickel of the core substrate 1 , and subsequent calculation of the weight of residual active material 3 within the core substrate exposed section 4 or 13 based on the rate of change in the weight of the dissolved active material 3 .
- the active material removal device 14 should preferably be operated with a gap C between the lower surface of the core substrate 1 and the contact surface 17 c of the ultrasound generation horn 17 a set to a value from 0.7 mm to 0.8 mm. Because the thickness D of the core substrate 1 following press working shown in FIG.
- the aforementioned gap C could be set to a smaller value than the range from 0.7 mm to 0.8 mm, although setting the gap to such a small value has no effect on the active material residual ratio. In contrast, if the aforementioned gap C is set to a value greater than the 0.7 mm to 0.8 mm range, then the active material residual ratio increases.
- the active material removal device 14 the active material 3 within the protrusion 8 is in a state which is easily removed, the core substrate 1 is able to be moved rapidly and continuously across the positionally fixed ultrasonic vibration device 17 while removal of the active material 3 takes place, and the active material 3 is suctioned away by the vacuum suction device 18 underneath the protrusion 8 , and as a result the active material 3 is removed efficiently, and the productivity improves markedly.
- the core substrate 1 can be moved at a rapid rate of approximately 450 mm/sec.
- this active material removal step if the movement speed of the core substrate 1 is set to a value slower than 50 mm/sec and the time taken in removing the active material 3 is extended, then not only does the productivity drop, but the core substrate 1 also begins to rupture and holes similar to worm holes begin to appear.
- the ultrasonic vibration device 17 is set and operated so as to produce an amplitude within a range from 25 to 50 ⁇ m. If the amplitude is smaller than this range, the time required for removal of the active material 3 lengthens, whereas if the amplitude is larger than the aforementioned range, then although the removal efficiency of the active material 3 improves, the metal skeleton of the core substrate 1 ruptures and the mechanical strength deteriorates, and consequently the current collecting function deteriorates, and furthermore the active material 3 from regions near to the core substrate exposed sections 13 is also partially stripped away, meaning the linearity of the boundary line between the core substrate exposed section 13 and the other regions also deteriorates.
- the active material removal step of the embodiment although the application of ultrasonic vibrations is used for removing the active material 3 , there is no deterioration in the strength of the core substrate 1 . This effect was confirmed by evaluation results from a tensile tester. In contrast, in cases in which the application of ultrasonic vibrations is used for removing the active material 3 impregnated in a conventional core substrate 1 , the strength of the core substrate 1 typically falls by 50 to 70%. The reason for this observation is that in the conventional manufacturing methods, a core substrate 1 impregnated with an active material 3 is subjected to press working prior to the application of ultrasonic vibrations to the regions to become current collectors, and consequently the active material 3 is in a state which is extremely difficult to remove.
- the active material 3 impregnated in the protrusions 8 , 8 which have undergone almost no press working, is removed, and moreover the ultrasonic vibrations are applied only to the top of the protruding protrusions 8 , 8 and have little effect on the other regions, and consequently the core substrate 1 suffers no deterioration in strength.
- the aforementioned core substrate exposed sections 13 are lightly compressed using a different press roller (not shown in the drawings) from that shown in FIG. 2A, to yield the state shown in FIG. 1E, in which the core substrate exposed sections 13 are level with the other regions containing impregnated active material 3 .
- a different press roller not shown in the drawings
- four battery electrode plates 19 shown in FIG. 1F are obtained. Each of these battery electrode plates 19 are of the same strip form, and have a boundary line 19 c along the length of the electrode plate between an active material impregnated section 19 a and a current collector 19 b from which the active material 3 has been removed.
- the linearity of the boundary line 19 c between the active material impregnated section 19 a and the current collector 19 b of a battery electrode plate 19 formed via the steps described above has a small error of no more than 0.2 mm, whereas a battery electrode plate 7 produced by a conventional method displays an error of up to 0.8 mm.
- a conventional manufacturing method has a pressing step following the impregnation of the active material 3 in which three pressing operations are performed in order to achieve a predetermined impregnation density
- only a single press working step, for forming the protrusions 8 , 8 shown in FIG. 1C on the core substrate 1 is performed.
- the core substrate exposed section 13 can be folded and then compressed to produce the current collector 19 b, and by so doing, the mechanical strength and the density of the current collector 19 b is increased, and moreover, the current collecting efficiency is also improved.
- the variation in the impregnation density of the active material impregnated section 19 a is suppressed to no more than 1.5%. This is because the active material 3 is impregnated into the smooth core substrate 1 prior to press working.
- a battery electrode plate 7 obtained by conventional method a core substrate 1 which has been press worked and includes surface irregularities is impregnated with the active material 3 , and so it is impossible to ensure a uniform degree of impregnation across the entire substrate, and the active material impregnated section 7 a displays a variation in impregnation density of at least 3.5%.
- FIG. 4 shows a nickel-metal hydride battery in which an electrode group 51 , including battery electrode plates 19 p, 19 q of a positive electrode and a negative electrode produced by the above-described method spirally wound with a separator 55 interposed therebetween, is housed inside a cylindrical battery case 52 .
- an electrode group 51 including battery electrode plates 19 p, 19 q of a positive electrode and a negative electrode produced by the above-described method spirally wound with a separator 55 interposed therebetween, is housed inside a cylindrical battery case 52 .
- a positive electrode terminal 56 of a sealing plate 57 , and the positive electrode plate 19 p are electrically connected via a lead
- the battery case 52 which functions as a negative electrode, and the negative electrode plate 19 q are electrically connected via a lead.
- the inside of the battery case 52 is filled with an electrolyte.
- FIG. 5A through FIG. 5G are perspective views showing the sequence of production steps in a method for manufacturing a battery electrode plate according to a second embodiment of the present invention.
- the aforementioned first embodiment described a method for manufacturing a battery electrode plate 19 for forming a spirally wound electrode group for use in a cylindrical battery
- this second embodiment relates to a method of manufacturing battery electrode plates for forming a laminated electrode group for use in a prismatic battery.
- FIG. 5A through FIG. 5G those components which are identical with, or equivalent to those shown in FIG. 1A through FIG. 1F are labeled with the same reference numerals.
- the active material 3 is impregnated into a totally flat core substrate 1 prior to press working, and so is impregnated with a uniform density throughout the entire core substrate 1 , and moreover because the surface of the core substrate 1 is not irregular, namely there are no elevation differences, the active material 3 is retained within the substrate without flowing, and consequently dries with the uniform impregnation density maintained.
- the entire surface of the core substrate 1 uniformly impregnated with the active material 3 is subjected to press working, and the thickness of the substrate is compressed to approximately half, and the sections which form core substrate exposed sections in subsequent steps are left as two parallel rail shaped protrusions 20 , 20 .
- a stripe roller press device (not shown in the drawings) of the same basic construction as the stripe roller press device 9 shown in FIG. 2A is used, and includes a working press roller with annular slots provided at positions corresponding to the protrusions 20 , 20 shown in FIG. 5C.
- an active material removal step the active material 3 impregnated within the two protrusions 20 , 20 is removed to form two core substrate exposed sections 21 , 21 .
- an active material removal device (not shown in the drawings) which has a construction almost identical with that of the active material removal device 14 including an ultrasonic vibration device 17 shown in FIG. 3A and FIG. 3B, and the processing performed is identical with that described for the first embodiment.
- the core substrate exposed sections 21 , 21 are then lightly compressed using a press roller (not shown in the drawings), in a similar manner to the first embodiment, to yield a state in which the core substrate exposed sections 21 , 21 are level with the other regions containing active material 3 . Subsequently, as shown in FIG. 5D, the aforementioned core substrate exposed sections 21 , 21 are further compressed using the press roller so that the upper surfaces thereof are at a lower level than the regions containing active material 3 . Next, a strip shaped lead, namely a lead hoop 22 , is seam welded to each of the core substrate exposed sections 21 , 21 . Finally, by cutting or punching along each of the cutting lines shown by alternate long and short dash lines in FIG.
- a plurality of battery electrode plates 23 shown in FIG. 5G are obtained.
- Each of these battery electrode plates 23 are of the same form, and include an active material impregnated section 23 a, a current collector 23 b from which the active material 3 has been removed, and a lead plate 23 c which is fixed to the current collector 23 b.
- This method for manufacturing a battery electrode plate 23 includes essentially the same steps as the first embodiment, and as such is capable of achieving similar effects to those described above for the first embodiment, and so high quality battery electrode plates 23 for use in a prismatic battery are produced with high productivity.
- the active material impregnated core substrate 1 without a welded lead hoop 22 could also be divided in two by cutting along the cutting line shown down the center of FIG. 5F, the core substrate exposed section 21 then folded over and compressed to form a current collector, and the substrate then divided into individual battery electrode plates.
- the aforementioned process increases the mechanical strength and the density of the current collector, and also improves the current collection efficiency, and consequently enables the formation of a stable lead fragment with the same high quality as the lead plate 23 c provided by cutting the lead hoop 22 .
- FIG. 6 shows a nickel-metal hydride battery in which an electrode group 53 , including battery electrode plates 23 p, 23 q of a positive electrode and a negative electrode produced by the above-described method laminated alternately with a separator 58 interposed therebetween, is housed inside a prismatic battery case 54 .
- an electrode group 53 including battery electrode plates 23 p, 23 q of a positive electrode and a negative electrode produced by the above-described method laminated alternately with a separator 58 interposed therebetween, is housed inside a prismatic battery case 54 .
- a positive electrode terminal 60 of a sealing plate 59 and the positive electrode plate 23 p are electrically connected via a lead
- the battery case 54 which functions as a negative electrode, and the negative electrode plate 23 q are electrically connected via a lead.
- the inside of the battery case 54 is filled with an electrolyte.
- a battery electrode plate is obtained in which there is no variation in the impregnation density of the active material, the boundary line between the active material impregnated section and the current collector is a true straight line, the residual ratio of the active material in the current collector is low, and the entire current collector has a predetermined width. Consequently, the present invention is very useful for producing, with good efficiency, a battery with a high degree of high rate discharge characteristics.
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Abstract
A battery electrode plate (19) is produced via an active material impregnation step for impregnating an entire porous core substrate shaped like a thin plate (1) with an active material (3), a pressing step for performing press working on the core substrate to form a plurality of rail shaped protrusions (8), an active material removal step for removing the active material to form core substrate exposed sections (13) by applying ultrasonic vibrations to the rail shaped protrusions, a flattening step for compressing the core substrate exposed sections down to an identical level with the other sections, and a cutting step for cutting predetermined sections including the core substrate exposed sections.
Description
- This is a divisional application of application Ser. No. 10/111,665, filed May 22, 2000.
- The present invention relates to a battery electrode plate used in a rechargeable battery such as a nickel metal hydride battery or a nickel cadmium battery, and more particularly to a method and apparatus for manufacturing a non-sintered battery electrode plate including a foamed metal core substrate impregnated with an active material, and a battery using such a battery electrode plate.
- Amongst electrode plates for rechargeable batteries, those produced using a foamed metal with a three dimensional network structure as a core substrate, by impregnating the core substrate with an active material, display comparatively superior discharge capacities, and are widely used. In addition, in recent years there has been strong demand for improvements in the high rate discharge characteristics of batteries, and as a result, new battery electrode plate manufacturing methods have been proposed, such as that shown in FIG. 7A to FIG. 7E disclosed in Japanese Laid-Open Patent Publication No. 2000-77054. Firstly, in a first pressing process, two
slots 2 of predetermined width are formed in acore substrate 1 composed of a foamed metal, with the two slots parallel with both edges of the core substrate. Once thecore substrate 1 has been impregnated with anactive material 3, theactive material 3 accumulated inside theslots 2 is removed using a brush or the like. Subsequently, in a second pressing process, thecore substrate 1 is subjected to three press working steps and converted to a form shown in FIG. 7C in which the entire surface is level with the bottom of theslots 2. The sections where theslots 2 had been formed are then subjected to an active material removal process using a brush and an air blower to form core substrate exposedsections 4 as shown in FIG. 7D. Thecore substrate 1 is then cut, formingbattery electrode plates 7. - A
current collector 7 b including the core substrate exposedsection 4 is formed on one edge of thebattery electrode plate 7, and a cylindrical electrode group formed by winding this electrode plate has a current collector on one end surface. Because this electrode group collects current uniformly along the entire length of the battery electrode plate, the current collecting efficiency improves. In addition, by employing a tab-less method wherein a current collecting lead plate is welded to the aforementioned current collector, the current collection characteristics improve markedly, enabling the demands for improvements in high rate discharge characteristics to be met. - However, the
battery electrode plate 7 prepared by the processes described above suffers from the problems described below. A first problem is that because variations in the impregnation density of theactive material 3 occur within active material impregnatedsections 7 a, there is a variation in the capacity of batteries produced using thesebattery electrode plates 7, and so when applied to a battery pack, there is an increased likelihood of over charging or over discharging. - A second problem is that because a
boundary line 7 c between the active material impregnatedsection 7 a and thecurrent collector 7 b is not a true straight line, the precision of the dimensions and shape of thebattery electrode plate 7 is low, leading to a reduction in the current collecting function of a battery produced using thisbattery electrode plate 7, and a failure to achieve high rate discharge characteristics. - A third problem is that because the removal of the
active material 3 from thecurrent collector 7 b is imperfect, there is an increased likelihood of unsatisfactory welding occurring during attachment of the current collecting lead plate to thecurrent collector 7 b, resulting in a reduced yield. Removal of the active material using a brush and air blower is also inefficient, and invites a reduction in productivity. - A fourth problem is that the width of the core substrate exposed
sections 4 shown in FIG. 7D, prior to cutting, differs from the preset value. As a result, a method wherein the core substrate exposed section is folded at right angles and then compressed to form the current collector cannot be applied, and so it becomes impossible to ensure the mechanical strength of the current collector or a high current collection efficiency. - A fifth problem is that the
battery electrode plates 7 obtained by cutting thecore substrate 1 are susceptible to warping into a bow shape. When thebattery electrode plate 7 is wound into a spiral shape to form an electrode group, this warping can be the cause of weaving, resulting in an electrode group of an unsatisfactory shape. Moreover, not only does this warping occur, but when viewed at magnification under a microscope, it is apparent that fine cracks also develop at the boundary section between the active material impregnatedsection 7 a and thecurrent collector 7 b, and sections of the metallic skeleton of thecore substrate 1 rupture, leading to a deterioration in strength. As a result, this type ofbattery electrode plate 7 is susceptible to problems such as dropout of theactive material 3, short circuiting, and deterioration in the electrical conductivity. - Japanese Laid-Open Patent Publication No. 2000-77054 discloses another method of manufacturing a battery electrode plate. This method involves impregnating an entire core substrate composed of a foamed metal with an active material, subsequently carrying out press working to compress the entire core substrate to a predetermined thickness, and then forming core substrate exposed sections by removing the active material from certain regions using an ultrasonic vibration device.
- However in this method, because the boundary line between the active material impregnated sections and the current collector of the battery electrode plate is not a true straight line, there is a deterioration in the current collecting function of a battery produced using this battery electrode plate, and high rate discharge characteristics are unobtainable. This is because a large amplitude ultrasonic vibration must be applied in order to remove the active material after the press working, and as a result, even the active material in the regions surrounding the core substrate exposed sections is removed. In addition, there is a danger that the metallic skeleton of the core substrate may suffer damage or deterioration when exposed to large amplitude ultrasonic vibrations.
- Consequently, the present invention takes the conventional problems described above into consideration, with an object of providing a method and apparatus for manufacturing a battery electrode plate in which there is no variation in the impregnation density of the active material, the boundary line between the active material impregnated sections and the current collector is a true straight line, the residual ratio of the active material in the current collector is low, and the entire current collector has a predetermined width, as well as providing a battery which utilizes such a battery electrode plate.
- In order to achieve the above object, a method for manufacturing a battery electrode plate according to the present invention includes an active material impregnation step for impregnating an entire porous core substrate shaped like a thin plate with an active material; a pressing step for performing press working on the active material impregnated core substrate to form a plurality of rail shaped protrusions; an active material removal step for removing the active material to form core substrate exposed sections by applying ultrasonic vibrations to the rail shaped protrusions; a flattening step for pressing down on the top of the core substrate exposed sections and compressing the exposed sections down to the same level as the other sections; and a cutting step for cutting predetermined sections including the core substrate exposed sections to form individual battery electrode plates.
- An electrode group produced by spirally winding the battery electrode plates of a positive and negative electrode produced by the above method, with a separator interposed therebetween, can be placed within a cylindrical battery case to form a cylindrical battery.
- Another method for manufacturing a battery electrode plate according to the invention includes an active material impregnation step for impregnating an entire porous core substrate shaped like a thin plate with an active material; a pressing step for performing press working on the active material impregnated core substrate to form a plurality of rail shaped protrusions; an active material removal step for removing the active material to form core substrate exposed sections by applying ultrasonic vibrations to the rail shaped protrusions; a core substrate exposed section compression step for compressing the core substrate exposed sections; a lead welding step for seam welding a lead hoop to the core substrate exposed sections; and a cutting step for cutting predetermined sections including the lead hoop to form individual battery electrode plates.
- An electrode group produced by alternately laminating the battery electrode plates of a positive and negative electrode produced by the above method, with a separator interposed therebetween, can be placed within a prismatic battery case to form a prismatic battery.
- An apparatus for manufacturing a battery electrode plate of the present invention includes a stripe roller press device for performing press working on an active material impregnated core substrate formed from a porous core substrate shaped like a thin plate, to form a plurality of rail shaped protrusions; and an active material removal device including an ultrasonic vibration device for bringing an ultrasound generation horn into contact with the rail shaped protrusions and applying ultrasonic vibrations and a vacuum suction device positioned in an opposing position below each ultrasonic vibration device for suctioning the active material removed by the application of ultrasonic vibrations.
- Another apparatus for manufacturing a battery electrode plate of the invention includes a stripe roller press device for performing press working on an active material impregnated core substrate formed from a porous core substrate shaped like a thin plate, to form a plurality of rail shaped protrusions; an active material removal device including an ultrasonic vibration device for bringing an ultrasound generation horn into contact with the rail shaped protrusions and applying ultrasonic vibrations and a vacuum suction device positioned in an opposing position below each ultrasonic vibration device for suctioning the active material removed by the application of ultrasonic vibrations; a welding device for seam welding a lead hoop to a core substrate exposed sections formed by the active material removal device; and a cutter for cutting predetermined sections including the lead hoop to form individual battery electrode plates.
- FIG. 1A, FIG. 1B, FIG. 1C, FIG. 1D, FIG. 1E and FIG. 1F are perspective views showing the sequence of production steps in a method for manufacturing a battery electrode plate according to a first embodiment of the present invention;
- FIG. 2A is a front view showing a stripe roller press device used in a pressing step of the above method, and FIG. 2B is an enlarged view of the portion IIB of FIG. 2A;
- FIG. 3A is a front view showing an active material removal device used in an active material removal step, and FIG. 3B is a right hand side view of the removal device;
- FIG. 4 is a partially cutaway perspective view showing a cylindrical battery containing a battery electrode plate produced by the above method;
- FIG. 5A, FIG. 5B, FIG. 5C, FIG. 5D, FIG. 5E, FIG. 5F and FIG. 5G are perspective views showing the sequence of production steps in a method for manufacturing a battery electrode plate according to a second embodiment of the invention;
- FIG. 6 is a partially cutaway perspective view of a prismatic battery containing a battery electrode plate produced by the above method; and
- FIG. 7A, FIG. 7B, FIG. 7C, FIG. 7D and FIG. 7E are perspective views showing the sequence of production steps in a conventional method for manufacturing a battery electrode plate.
- As follows is a description of preferred embodiments of the present invention, with reference to the drawings. FIG. 1A through FIG. 1F are perspective views showing the sequence of production steps in a method for manufacturing a battery electrode plate according to a first embodiment of the invention. First, an
entire core substrate 1 formed from a rectangular sheet of foamed metal of a predetermined size, shown in FIG. 1A, is impregnated with anactive material 3 as shown in FIG. 1B. Theactive material 3 is impregnated into the totallyflat core substrate 1 prior to press working, and so is impregnated with a uniform density throughout theentire core substrate 1, and moreover because the surface of thecore substrate 1 is not irregular, namely there are no elevation differences, theactive material 3 is retained within the substrate without flowing, and consequently dries with the uniform impregnation density maintained. In this embodiment, thecore substrate 1 is a foamed nickel metal with a three dimensional network structure, and is formed as a rectangular thin sheet with a thickness of 1.24 mm, for example. However, the manufacturing method of this embodiment should preferably be applied to a continuous strip type core substrate, namely a hoop core substrate. - Next, as shown in FIG. 1C, the entire surface of the
core substrate 1 with the exception of those sections which form core substrate exposedsections 13 in subsequent steps, is subjected to press working, and the thickness of the substrate is compressed to approximately half, from the aforementioned 1.24 mm, down to 0.6 mm for example. At this point, two parallel rail shapedprotrusions - FIG. 2A is a front view of the stripe roller press device9, and FIG. 2B is an enlarged view of the portion IIB of FIG. 2A. The stripe roller press device 9 includes a supporting
press roller 10 and a workingpress roller 11, wherein the supportingpress roller 10 is supported at a fixed position but is free to rotate, and the workingpress roller 11 is subjected to a predetermined pressure toward thepress roller 10. Accordingly, the workingpress roller 11 possesses a rigidity capable of withstanding the applied pressure, and is provide withannular slots protrusions side walls annular slots 12 are curved surfaces with a radius of curvature R of 0.3 mm to 0.6 mm, for example. - Furthermore, the two
press rollers core substrate 1 which passes between the twopress rollers protrusions annular slots 12, and conforms precisely to the preset value. - Whereas a conventional method for manufacturing a battery electrode plate includes two pressing steps, in the manufacturing method of this embodiment, only one pressing step is needed for forming the two
protrusions active material 3 described above. As a result, experimental results revealed that 3 ton of load was necessary per 1 cm width of electrode plate. In practice, in order to ensure a uniform width for theprotrusion 8 along the entire substrate, the gap between the twopress rollers - Furthermore, because a foamed metal formed from pure nickel, which displays excellent expansibility, is used for the
core substrate 1, during the pressing step, those portions with a high impregnation density of theactive material 3 display a larger degree of elongation. This variation in elongation is suppressed by increasing the roller diameter of thepress rollers press rollers core substrate 1 will be. The reason for this observation is that the larger the diameter of the press rollers become, the closer the process will be to flat press working. Consequently, ifpress rollers active material 3 is suppressed. - Furthermore, in the second pressing step of the conventional manufacturing method, pressing is performed three times using a relatively small press roller with a diameter of 400 mm, and produces a lengthwise elongation of as much as 6%. This elongation is the cause of the bow shaped warping which occurs when the
core substrate 1 is divided into individualbattery electrode plates 7. In contrast, in the pressing step of the manufacturing method according to this embodiment, because only a single press working process is performed usingpress rollers core substrate 1 is divided into individualbattery electrode plates 19 in a subsequent step, almost no warping or cracking occurs. - Moreover, in the pressing step, because the opening rim sections of the two
side walls annular slots 12 formed in the workingpress roller 11 are curved surfaces with a radius of curvature R of 0.3 mm to 0.6 mm, the boundaries between theprotrusions core substrate 1 does not occur during the press working. If the radius of curvature R of the curved surfaces is set to a value greater than the range from 0.3 mm to 0.6 mm, theactive material 3 of the edge of theprotrusions protrusions core substrate 1, and a battery produced using such a battery electrode plate would display a reduced current collecting efficiency. - Subsequently, in an active material removal step shown in FIG. 1D, the
active material 3 impregnated within the twoprotrusions sections material removal device 14 used in this step, wherein FIG. 3A is a front view and FIG. 3B is a right hand side view. The activematerial removal device 14 includes a pair ofultrasonic vibration devices active material 3 by bringingultrasound generation horns protrusions vacuum suction devices ultrasonic vibration devices active material 3 which has been stripped away and removed. - The
ultrasound generation horns 17 a have a slopedsurface 17 b, with a downhill pitch in the direction of the movement of thecore substrate 1, at the contact surface with thecore substrate 1, and this slopedsurface 17 b prevents damage to thecore substrate 1. Furthermore, in order to reduce abrasion, the slopedsurface 17 b, and aflat contact surface 17 c which is a continuation of the slopedsurface 17 b, are formed using sintered carbides, and the main body of theultrasound generation horn 17 a is formed from titanium. - According to this active
material removal device 14, thecore substrate 1 is moved in the direction of the arrow shown in FIG. 3B, with the tops of theprotrusions ultrasound generation horns 17 a of the pair of positionally fixedultrasonic vibration devices protrusion 8, the metal skeleton is squeezed and theactive material 3 contained therein is stripped away and removed, while at the same time, thevacuum suction device 18 suctions out and removesactive material 3 impregnated within theprotrusion 8 and the region below the protrusion. As a result, theactive material 3 contained within theprotrusion 8 and the region therebelow is almost entirely removed, yielding a high quality core substrate exposedsection 13. - As follows is a description of the reasons the residual ratio of
active material 3 within the core substrate exposedsection 13 is extremely low. Theactive material 3 to be removed in the aforementioned active material removal step is the active material impregnated within theprotrusion 8, and because theprotrusion 8 has not been subjected to press working, theactive material 3 is extremely easy to remove. Consequently, even in the case ofactive material 3 which contains a binder, which has proved extremely difficult to remove using conventional methods, by applying ultrasonic vibration to the substrate by bringing theultrasound generation horn 17 a of theultrasonic vibration device 17 into contact with the substrate while applying suction from below with thevacuum suction device 18, theactive material 3 is removed easily and completely. - According to actual measurements, the active material residual ratio of a core substrate exposed
section 13 formed through the aforementioned active material removal step is from 1 to 4%. In comparison, the active material residual ratio of a core substrate exposedsection 4 formed in the conventional manufacturing method is much higher, at 10% or more, and furthermore lumps ofactive material 3 still exist, and these lumps are the main cause of spark generation during the welding of the current collecting lead plates. Accordingly, these lumps are removed by hand, which leads to a further reduction in productivity. Evaluation of the active material residual ratios described above was conducted by immersion into an aqueous solution of acetic acid, which dissolves only theactive material 3 without dissolving the nickel of thecore substrate 1, and subsequent calculation of the weight of residualactive material 3 within the core substrate exposedsection active material 3. - In order to reduce the active material residual ratio of the core substrate exposed
section 13, in the case in which the thickness B of the rail shapedprotrusion 8 is approximately 1.1 mm, and the thickness D of thecore substrate 1 following press working is approximately 0.6 mm, the activematerial removal device 14 should preferably be operated with a gap C between the lower surface of thecore substrate 1 and thecontact surface 17 c of theultrasound generation horn 17 a set to a value from 0.7 mm to 0.8 mm. Because the thickness D of thecore substrate 1 following press working shown in FIG. 1C is precisely 0.58 mm, the aforementioned gap C could be set to a smaller value than the range from 0.7 mm to 0.8 mm, although setting the gap to such a small value has no effect on the active material residual ratio. In contrast, if the aforementioned gap C is set to a value greater than the 0.7 mm to 0.8 mm range, then the active material residual ratio increases. - In addition, in the active
material removal device 14, theactive material 3 within theprotrusion 8 is in a state which is easily removed, thecore substrate 1 is able to be moved rapidly and continuously across the positionally fixedultrasonic vibration device 17 while removal of theactive material 3 takes place, and theactive material 3 is suctioned away by thevacuum suction device 18 underneath theprotrusion 8, and as a result theactive material 3 is removed efficiently, and the productivity improves markedly. According to actual measurements, because theactive material 3 is in a state which is easily removed, thecore substrate 1 can be moved at a rapid rate of approximately 450 mm/sec. In this active material removal step, if the movement speed of thecore substrate 1 is set to a value slower than 50 mm/sec and the time taken in removing theactive material 3 is extended, then not only does the productivity drop, but thecore substrate 1 also begins to rupture and holes similar to worm holes begin to appear. - Furthermore, in the active material removal step, the
ultrasonic vibration device 17 is set and operated so as to produce an amplitude within a range from 25 to 50 μm. If the amplitude is smaller than this range, the time required for removal of theactive material 3 lengthens, whereas if the amplitude is larger than the aforementioned range, then although the removal efficiency of theactive material 3 improves, the metal skeleton of thecore substrate 1 ruptures and the mechanical strength deteriorates, and consequently the current collecting function deteriorates, and furthermore theactive material 3 from regions near to the core substrate exposedsections 13 is also partially stripped away, meaning the linearity of the boundary line between the core substrate exposedsection 13 and the other regions also deteriorates. - In the active material removal step of the embodiment, although the application of ultrasonic vibrations is used for removing the
active material 3, there is no deterioration in the strength of thecore substrate 1. This effect was confirmed by evaluation results from a tensile tester. In contrast, in cases in which the application of ultrasonic vibrations is used for removing theactive material 3 impregnated in aconventional core substrate 1, the strength of thecore substrate 1 typically falls by 50 to 70%. The reason for this observation is that in the conventional manufacturing methods, acore substrate 1 impregnated with anactive material 3 is subjected to press working prior to the application of ultrasonic vibrations to the regions to become current collectors, and consequently theactive material 3 is in a state which is extremely difficult to remove. In contrast, in this embodiment, theactive material 3 impregnated in theprotrusions protrusions core substrate 1 suffers no deterioration in strength. - Next, the aforementioned core substrate exposed
sections 13 are lightly compressed using a different press roller (not shown in the drawings) from that shown in FIG. 2A, to yield the state shown in FIG. 1E, in which the core substrate exposedsections 13 are level with the other regions containing impregnatedactive material 3. Finally, by cutting along the three cutting lines shown by alternate long and short dash lines in FIG. 1E, fourbattery electrode plates 19 shown in FIG. 1F are obtained. Each of thesebattery electrode plates 19 are of the same strip form, and have aboundary line 19 c along the length of the electrode plate between an active material impregnatedsection 19 a and acurrent collector 19 b from which theactive material 3 has been removed. - According to actual measurements using a microscope, the linearity of the
boundary line 19 c between the active material impregnatedsection 19 a and thecurrent collector 19 b of abattery electrode plate 19 formed via the steps described above has a small error of no more than 0.2 mm, whereas abattery electrode plate 7 produced by a conventional method displays an error of up to 0.8 mm. The reason for this observation is that whereas a conventional manufacturing method has a pressing step following the impregnation of theactive material 3 in which three pressing operations are performed in order to achieve a predetermined impregnation density, in the manufacturing method of this embodiment, only a single press working step, for forming theprotrusions core substrate 1, is performed. Accordingly, in thebattery electrode plate 19 obtained in the embodiment, the core substrate exposedsection 13 can be folded and then compressed to produce thecurrent collector 19 b, and by so doing, the mechanical strength and the density of thecurrent collector 19 b is increased, and moreover, the current collecting efficiency is also improved. - Furthermore, in the
battery electrode plate 19, the variation in the impregnation density of the active material impregnatedsection 19 a is suppressed to no more than 1.5%. This is because theactive material 3 is impregnated into thesmooth core substrate 1 prior to press working. In contrast, in abattery electrode plate 7 obtained by conventional method, acore substrate 1 which has been press worked and includes surface irregularities is impregnated with theactive material 3, and so it is impossible to ensure a uniform degree of impregnation across the entire substrate, and the active material impregnatedsection 7 a displays a variation in impregnation density of at least 3.5%. - FIG. 4 shows a nickel-metal hydride battery in which an
electrode group 51, includingbattery electrode plates 19 p, 19 q of a positive electrode and a negative electrode produced by the above-described method spirally wound with aseparator 55 interposed therebetween, is housed inside acylindrical battery case 52. In this cylindrical battery, apositive electrode terminal 56 of a sealingplate 57, and thepositive electrode plate 19 p are electrically connected via a lead, and thebattery case 52 which functions as a negative electrode, and the negative electrode plate 19 q are electrically connected via a lead. The inside of thebattery case 52 is filled with an electrolyte. - FIG. 5A through FIG. 5G are perspective views showing the sequence of production steps in a method for manufacturing a battery electrode plate according to a second embodiment of the present invention. The aforementioned first embodiment described a method for manufacturing a
battery electrode plate 19 for forming a spirally wound electrode group for use in a cylindrical battery, whereas this second embodiment relates to a method of manufacturing battery electrode plates for forming a laminated electrode group for use in a prismatic battery. In FIG. 5A through FIG. 5G, those components which are identical with, or equivalent to those shown in FIG. 1A through FIG. 1F are labeled with the same reference numerals. - First, an
entire core substrate 1 formed from a rectangular or strip shaped piece of foamed metal of a predetermined size, as shown in FIG. 5A, is impregnated with anactive material 3 as shown in FIG. 5B. In this case, theactive material 3 is impregnated into a totallyflat core substrate 1 prior to press working, and so is impregnated with a uniform density throughout theentire core substrate 1, and moreover because the surface of thecore substrate 1 is not irregular, namely there are no elevation differences, theactive material 3 is retained within the substrate without flowing, and consequently dries with the uniform impregnation density maintained. - Next, as shown in FIG. 5C, the entire surface of the
core substrate 1 uniformly impregnated with theactive material 3, with the exception of those sections which form core substrate exposed sections in subsequent steps, is subjected to press working, and the thickness of the substrate is compressed to approximately half, and the sections which form core substrate exposed sections in subsequent steps are left as two parallel rail shapedprotrusions protrusions - Subsequently, in an active material removal step, the
active material 3 impregnated within the twoprotrusions sections material removal device 14 including anultrasonic vibration device 17 shown in FIG. 3A and FIG. 3B, and the processing performed is identical with that described for the first embodiment. - The core substrate exposed
sections sections active material 3. Subsequently, as shown in FIG. 5D, the aforementioned core substrate exposedsections active material 3. Next, a strip shaped lead, namely alead hoop 22, is seam welded to each of the core substrate exposedsections battery electrode plates 23 shown in FIG. 5G are obtained. Each of thesebattery electrode plates 23 are of the same form, and include an active material impregnatedsection 23 a, acurrent collector 23 b from which theactive material 3 has been removed, and alead plate 23 c which is fixed to thecurrent collector 23 b. - This method for manufacturing a
battery electrode plate 23 includes essentially the same steps as the first embodiment, and as such is capable of achieving similar effects to those described above for the first embodiment, and so high qualitybattery electrode plates 23 for use in a prismatic battery are produced with high productivity. Moreover, instead of the step for welding thelead hoop 22, the active material impregnatedcore substrate 1 without a weldedlead hoop 22 could also be divided in two by cutting along the cutting line shown down the center of FIG. 5F, the core substrate exposedsection 21 then folded over and compressed to form a current collector, and the substrate then divided into individual battery electrode plates. The aforementioned process increases the mechanical strength and the density of the current collector, and also improves the current collection efficiency, and consequently enables the formation of a stable lead fragment with the same high quality as thelead plate 23 c provided by cutting thelead hoop 22. - FIG. 6 shows a nickel-metal hydride battery in which an
electrode group 53, includingbattery electrode plates 23 p, 23 q of a positive electrode and a negative electrode produced by the above-described method laminated alternately with aseparator 58 interposed therebetween, is housed inside aprismatic battery case 54. In this prismatic battery, apositive electrode terminal 60 of a sealingplate 59, and thepositive electrode plate 23 p are electrically connected via a lead, and thebattery case 54 which functions as a negative electrode, and the negative electrode plate 23 q are electrically connected via a lead. The inside of thebattery case 54 is filled with an electrolyte. - According to the present invention, a battery electrode plate is obtained in which there is no variation in the impregnation density of the active material, the boundary line between the active material impregnated section and the current collector is a true straight line, the residual ratio of the active material in the current collector is low, and the entire current collector has a predetermined width. Consequently, the present invention is very useful for producing, with good efficiency, a battery with a high degree of high rate discharge characteristics.
Claims (2)
1. A cylindrical battery comprising:
an electrode group formed from battery electrode plates of a positive electrode and a negative electrode spirally wound with a separator interposed therebetween; and
a cylindrical battery case for housing said electrode group;
at least one of the battery electrode plates being manufactured by a method comprising:
an active material impregnation step for impregnating an entire porous core substrate shaped like a thin plate with an active material;
a pressing step for performing press working on said active material impregnated core substrate to form a plurality of rail shaped protrusions;
an active material removal step for removing the active material to form core substrate exposed sections by applying ultrasonic vibrations to said rail shaped protrusions;
a flattening step for compressing said core substrate exposed sections down to an identical level with other sections; and
a cutting step for cutting predetermined sections including said core substrate exposed sections to form a battery electrode plate.
2. A cylindrical battery according to claim 1 , in which the positive and the negative electrode plates are manufactured by said method.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/823,863 US20040191613A1 (en) | 2000-08-30 | 2004-04-14 | Method and apparatus for manufacturing battery electrode plate and battery using the same |
US12/291,848 US20090081533A1 (en) | 2000-08-30 | 2008-11-14 | Method and apparatus for manufacturing battery electrode plate and battery using the same |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2000-261471 | 2000-08-30 | ||
JP2000261471A JP4023990B2 (en) | 2000-08-30 | 2000-08-30 | Method and apparatus for manufacturing battery electrode plate |
US10/111,665 US6878173B2 (en) | 2000-08-30 | 2001-08-29 | Method for manufacturing electrode plate for cell |
US10/823,863 US20040191613A1 (en) | 2000-08-30 | 2004-04-14 | Method and apparatus for manufacturing battery electrode plate and battery using the same |
Related Parent Applications (2)
Application Number | Title | Priority Date | Filing Date |
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US10/111,665 Division US6878173B2 (en) | 2000-08-30 | 2001-08-29 | Method for manufacturing electrode plate for cell |
PCT/JP2001/007444 Division WO2002019447A1 (en) | 2000-08-30 | 2001-08-29 | Method and device for manufacturing electrode plate for cell, and cell using the electrode plate |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US12/291,848 Continuation US20090081533A1 (en) | 2000-08-30 | 2008-11-14 | Method and apparatus for manufacturing battery electrode plate and battery using the same |
Publications (1)
Publication Number | Publication Date |
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US20040191613A1 true US20040191613A1 (en) | 2004-09-30 |
Family
ID=18749307
Family Applications (4)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/111,665 Expired - Fee Related US6878173B2 (en) | 2000-08-30 | 2001-08-29 | Method for manufacturing electrode plate for cell |
US10/823,863 Abandoned US20040191613A1 (en) | 2000-08-30 | 2004-04-14 | Method and apparatus for manufacturing battery electrode plate and battery using the same |
US10/823,919 Abandoned US20040191620A1 (en) | 2000-08-30 | 2004-04-14 | Method and apparatus for manufacturing battery electrode plate and battery using the same |
US12/291,848 Abandoned US20090081533A1 (en) | 2000-08-30 | 2008-11-14 | Method and apparatus for manufacturing battery electrode plate and battery using the same |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
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US10/111,665 Expired - Fee Related US6878173B2 (en) | 2000-08-30 | 2001-08-29 | Method for manufacturing electrode plate for cell |
Family Applications After (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/823,919 Abandoned US20040191620A1 (en) | 2000-08-30 | 2004-04-14 | Method and apparatus for manufacturing battery electrode plate and battery using the same |
US12/291,848 Abandoned US20090081533A1 (en) | 2000-08-30 | 2008-11-14 | Method and apparatus for manufacturing battery electrode plate and battery using the same |
Country Status (8)
Country | Link |
---|---|
US (4) | US6878173B2 (en) |
EP (1) | EP1317007B1 (en) |
JP (1) | JP4023990B2 (en) |
KR (1) | KR100438262B1 (en) |
CN (1) | CN1206755C (en) |
DE (1) | DE60133472T2 (en) |
TW (1) | TW511312B (en) |
WO (1) | WO2002019447A1 (en) |
Cited By (1)
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US11217780B2 (en) | 2016-06-27 | 2022-01-04 | Samsung Sdi Co., Ltd. | Method for manufacturing secondary battery and secondary battery using same |
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JP4023990B2 (en) * | 2000-08-30 | 2007-12-19 | 松下電器産業株式会社 | Method and apparatus for manufacturing battery electrode plate |
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US8865345B1 (en) | 2007-01-12 | 2014-10-21 | Enovix Corporation | Electrodes for three-dimensional lithium batteries and methods of manufacturing thereof |
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US9166230B1 (en) | 2007-01-12 | 2015-10-20 | Enovix Corporation | Three-dimensional battery having current-reducing devices corresponding to electrodes |
US8663730B1 (en) | 2007-01-12 | 2014-03-04 | Enovix Corporation | Method to fabricate a three dimensional battery with a porous dielectric separator |
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CN101584065B (en) | 2007-01-12 | 2013-07-10 | 易诺维公司 | Three-dimensional batteries and methods of manufacturing the same |
DE102008055775A1 (en) * | 2008-11-04 | 2010-05-06 | Vb Autobatterie Gmbh & Co. Kgaa | Electrode for a rechargeable battery |
US8011559B2 (en) * | 2009-11-09 | 2011-09-06 | GM Global Technology Operations LLC | Active material-augmented vibration welding system and method of use |
JP5461267B2 (en) * | 2010-03-26 | 2014-04-02 | 三菱重工業株式会社 | Electrode plate manufacturing apparatus and electrode plate manufacturing method |
KR101124964B1 (en) * | 2010-04-28 | 2012-03-27 | 주식회사 이아이지 | Method for connecting between cathod lead or anode lead of secondary battery and external element |
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JP2012186134A (en) * | 2011-02-18 | 2012-09-27 | Sumitomo Electric Ind Ltd | Three-dimensional net-like aluminum porous body for current collector and method of manufacturing the same |
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JP5228133B1 (en) * | 2012-10-01 | 2013-07-03 | 株式会社日立エンジニアリング・アンド・サービス | Roll press facility for electrode material and method for producing electrode sheet |
JPWO2017018347A1 (en) * | 2015-07-28 | 2018-05-17 | Necエナジーデバイス株式会社 | Electrode sheet manufacturing method |
JP7070436B2 (en) * | 2017-01-24 | 2022-05-18 | 三洋電機株式会社 | Battery plate manufacturing method, battery manufacturing method, and battery |
CN217788446U (en) * | 2022-05-16 | 2022-11-11 | 宁德时代新能源科技股份有限公司 | Mark making device and pole piece production system |
KR102663774B1 (en) * | 2022-12-21 | 2024-05-03 | 주식회사 엘지에너지솔루션 | Coating layer treatment device for dry electrode and dry electrode manufacturing system including same |
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US4115627A (en) * | 1977-08-15 | 1978-09-19 | United Technologies Corporation | Electrochemical cell comprising a ribbed electrode substrate |
US4426340A (en) * | 1981-09-29 | 1984-01-17 | United Technologies Corporation | Process for fabricating ribbed electrode substrates and other articles |
JPH0770311B2 (en) | 1985-12-10 | 1995-07-31 | 松下電器産業株式会社 | Battery electrode manufacturing method |
JPS6340253A (en) | 1986-08-04 | 1988-02-20 | Sanyo Electric Co Ltd | Manufacture of electrode for battery |
US5045415A (en) * | 1988-12-13 | 1991-09-03 | Pita Witehira | Electrode plate structure |
JP3261688B2 (en) * | 1994-08-23 | 2002-03-04 | キヤノン株式会社 | Secondary battery and method of manufacturing the same |
JPH0963575A (en) | 1995-08-30 | 1997-03-07 | Furukawa Electric Co Ltd:The | Manufacture of electrode plate for battery |
DE69711269T2 (en) * | 1996-06-17 | 2002-10-24 | Dainippon Printing Co Ltd | Process for producing porous coating and process for producing an electrode plate for secondary battery with non-aqueous electrolyte |
JPH10247493A (en) | 1997-03-04 | 1998-09-14 | Matsushita Electric Ind Co Ltd | Manufacture of battery electrode and alkaline storage battery |
JP2000077054A (en) | 1998-09-01 | 2000-03-14 | Sanyo Electric Co Ltd | Battery and its manufacture |
JP4023990B2 (en) * | 2000-08-30 | 2007-12-19 | 松下電器産業株式会社 | Method and apparatus for manufacturing battery electrode plate |
-
2000
- 2000-08-30 JP JP2000261471A patent/JP4023990B2/en not_active Expired - Lifetime
-
2001
- 2001-08-29 KR KR10-2002-7005535A patent/KR100438262B1/en not_active IP Right Cessation
- 2001-08-29 DE DE60133472T patent/DE60133472T2/en not_active Expired - Lifetime
- 2001-08-29 CN CNB018026087A patent/CN1206755C/en not_active Expired - Fee Related
- 2001-08-29 WO PCT/JP2001/007444 patent/WO2002019447A1/en active IP Right Grant
- 2001-08-29 US US10/111,665 patent/US6878173B2/en not_active Expired - Fee Related
- 2001-08-29 EP EP01961179A patent/EP1317007B1/en not_active Expired - Lifetime
- 2001-08-30 TW TW090121442A patent/TW511312B/en not_active IP Right Cessation
-
2004
- 2004-04-14 US US10/823,863 patent/US20040191613A1/en not_active Abandoned
- 2004-04-14 US US10/823,919 patent/US20040191620A1/en not_active Abandoned
-
2008
- 2008-11-14 US US12/291,848 patent/US20090081533A1/en not_active Abandoned
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11217780B2 (en) | 2016-06-27 | 2022-01-04 | Samsung Sdi Co., Ltd. | Method for manufacturing secondary battery and secondary battery using same |
Also Published As
Publication number | Publication date |
---|---|
KR20020043258A (en) | 2002-06-08 |
EP1317007B1 (en) | 2008-04-02 |
US20040191620A1 (en) | 2004-09-30 |
JP2002075345A (en) | 2002-03-15 |
CN1206755C (en) | 2005-06-15 |
JP4023990B2 (en) | 2007-12-19 |
DE60133472D1 (en) | 2008-05-15 |
US20020182483A1 (en) | 2002-12-05 |
US6878173B2 (en) | 2005-04-12 |
CN1388994A (en) | 2003-01-01 |
TW511312B (en) | 2002-11-21 |
DE60133472T2 (en) | 2009-05-20 |
KR100438262B1 (en) | 2004-07-02 |
US20090081533A1 (en) | 2009-03-26 |
EP1317007A1 (en) | 2003-06-04 |
WO2002019447A1 (en) | 2002-03-07 |
EP1317007A4 (en) | 2007-08-08 |
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