Patent Application
20240047698
The present invention relates to lead foil and a bipolar lead acid storage battery.
A bipolar lead acid storage battery includes a bipolar electrode including a positive electrode, a negative electrode, and a substrate (collectively a bipolar plate). The positive electrode is provided on one surface of the substrate, and the negative electrode is provided on the other surface of the substrate. In a conventional bipolar electrode, lead foil is provided on both surfaces of a resin substrate, and a positive electrode and a negative electrode are provided on one surface and the other surface of the substrate, respectively. For example, JP Patent Publication No. 2004-158433 A discloses a lead alloy substrate having a surface roughness of 15 μm or more for the electrodes of a lead acid storage battery.
Meanwhile, in bipolar lead acid storage batteries, lead foil and a resin substrate are bonded by an adhesive. If sulfuric acid infiltrates the bonding interface, the adhesive is chemically degraded. Furthermore, the lead foil undergoes growth deformation that expands with long-term use of the battery. Therefore, the synergistic effect of the chemical degradation of the adhesive and the gross of the lead foil decreases the adhesive strength between the lead foil and the substrate. When the adhesive strength decreases, the lead foil peels away from the substrate, which causes a liquid junction path and results in a drop in battery voltage.
Therefore, the present invention has been made in view of the above problems, and an object of the present invention is to provide a lead foil and a bipolar lead acid storage battery capable of suppressing a voltage drop in the battery due to peeling of the lead foil from a substrate.
According to an aspect of the present invention, there is provided a lead foil for a current collector in a bipolar lead acid storage battery, in which a back face of the lead foil opposed to a substrate of the bipolar lead acid storage battery has a contact length of 150 μm or more and 1800 μm or less (i.e., between 150 μm and 1800 μm, inclusive) in a profile curve acquired, orthogonally to a rolling direction, by surface roughness measurement with a stylus, and with a scanning distance of 4 mm and a measurement interval of 0.5 μm. The contact length is a sum total of respective absolute values of differences in height between adjacent measurement points.
According to an aspect of the present invention, there is provided a bipolar lead acid storage battery in which at least one of a positive lead foil or a negative lead foil is the above lead foil.
According to an aspect of the present invention, there are provided a lead foil and a bipolar lead acid storage battery capable of suppressing a voltage drop in the battery due to peeling of the lead foil from a substrate.
In the following detailed description, embodiments of the present invention will be described with reference to the drawings. In the description of the drawings, the same or similar portions are denoted by the same or similar reference signs, and redundant description is omitted. Each drawing is schematic and includes a case different from an actual case. In addition, the embodiments described below illustrate apparatuses and methods for embodying the technical idea of the present invention, and the technical idea of the present invention does not specify the materials, structures, arrangements, and the like of the components as follows. Various modifications can be made to the technical idea of the present invention within the technical scope defined by the claims.
Bipolar Lead Acid Storage Battery
A structure of a bipolar lead acid storage battery 1 according to an embodiment of the present invention will be described with reference to
The second plate units and the third plate units are alternately stacked between the first plate unit and the fourth plate unit to form the bipolar lead acid storage battery 1 having a substantially rectangular parallelepiped shape. The number of the stacked second plate units and the number of the stacked third plate units are set such that the storage capacity of the bipolar lead acid storage battery 1 has a desired value.
A negative terminal 107 is fixed to the first plate 11. The negative electrode 110 and the negative terminal 107 that are fixed to the first plate 11 are electrically connected.
A positive terminal 108 is fixed to the fourth plate 14. The positive electrode 120 and the positive terminal 108 that are fixed to the fourth plate 14 are electrically connected.
The electrolytic layer 105 is formed of, for example, a glass fiber mat impregnated with an electrolyte containing sulfuric acid.
The first plate 11, the second plate 12, the third plate 13, and the fourth plate 14 are formed of, for example, a known molding resin. The first plate 11, the second plate 12, the third plate 13, and the fourth plate 14 are fixed to each other by an appropriate method such that the inside is sealed to prevent the electrolyte from flowing out.
The positive electrode 120 includes a positive lead foil 101 made of lead or a lead alloy and disposed on the one surface of the substrate 111, a positive active material layer 103 disposed on the positive lead foil 101, and an adhesive layer 140 disposed between the one surface of the substrate 111 and the positive lead foil 101 to bond the one surface of the substrate 111 to the positive lead foil 101. That is, on the one surface of the substrate 111 (upward-facing surface of the paper in
The negative electrode 110 includes a negative lead foil 102 made of lead or a lead alloy and disposed on the other surface of the substrate 111, a negative active material layer 104 disposed on the negative lead foil 102, and an adhesive layer (not illustrated) disposed between the other surface of the substrate 111 and the negative lead foil 102 to bond the other surface of the substrate 111 to the negative lead foil 102.
The positive electrode 120 and the negative electrode 110 are electrically connected by an appropriate method.
Note that, in the cross-sectional view of the bipolar electrode illustrated in
In the bipolar lead acid storage battery 1 having such a configuration, the substrate 111, the positive lead foil 101, the positive active material layer 103, the negative lead foil 102, and the negative active material layer 104 constitute the bipolar electrode 130, as previously described. The bipolar electrode is an electrode, a single one of which functions as both a positive electrode and a negative electrode.
The bipolar lead acid storage battery 1 has a battery configuration in which a plurality of cell members are connected in series by alternately stacking and assembling the cell members in which the electrolytic layer 105 is interposed between the positive electrode 120 and the negative electrode 110.
Furthermore, in the bipolar lead acid storage battery 1 according to the present embodiment, the adhesive layer 140 disposed between the one surface of the substrate 111, and the positive lead foil 101 is formed of a cured product of a reaction-curable adhesive that is cured by reaction of a main agent containing an epoxy resin with a curing agent containing an amine compound.
Lead Foil
The lead foil according to the present embodiment is the positive lead foil 101 and the negative lead foil 102 in the above bipolar lead acid storage battery 1, that is, lead foil for a current collector in the bipolar lead acid storage battery 1. In the present embodiment, one surface of the lead foil that faces and is in contact with the positive active material layer 103 or the negative active material layer 104 is defined as a front surface, and the other surface of the lead foil that faces and is in contact with the substrate 111 is defined as a back surface. In addition, the lead foil is produced to have a predetermined thickness by being rolled with a rolling roll.
The back surface of the lead foil has a contact length X of 150 μm or more and 1800 μm or less (i.e., between 150 μm and 1800 μm, inclusive) in a profile curve acquired, orthogonally to a rolling direction at the time of rolling, by surface roughness measurement with a stylus. The surface roughness measurement with a stylus can be performed by the measurement method specified in JIS B 0601:1994. When the lead foil is measured by this measurement method, a profile curve as illustrated in
As described above, the peeling of the lead foil from the substrate is greatly affected by infiltration of sulfuric acid from the end surface of the electrode into the bonding interface between the lead foil and the substrate. Furthermore, the inventors conducted an Electron probe micro-analyzer (EPMA) analysis on an electrode in which the peeling occurred due to the use of a battery and confirmed from the detected components of sulfuric acid that sulfuric acid infiltrated between the lead foil and the adhesive layer. That is, a penetration route of sulfuric acid is an interface between the lead foil (e.g., the positive lead foil 101) and the adhesive layer 140, as illustrated in
The contact length X may be increased by changing the height of the roughness of the back surface of the lead foil or may be increased by narrowing the pitch of irregularities without changing the height of the roughness. As illustrated in
In addition, because sulfuric acid infiltrates from the end surface side of the electrode (e.g., the positive electrode 120 or the negative electrode 110), the contact length X may be set within the above range only at the outer circumferential edge portion of the lead foil. The outer circumferential edge portion of the lead foil is, for example, a region outside the region surrounded by a dotted line in the positive lead foil 101 illustrated in
The lead foil is made of lead or a lead alloy containing lead as a main component. It is preferable that the lead foil contains Sn, and the content of Sn is 0.4% by mass or more and 2% by mass or less (i.e., between 0.4% by mass and 2% by mass, inclusive). When Sn is contained in the lead foil, the adhesion between the lead foil and the active material can be improved. If the content of Sn is less than 0.4% by mass, the adhesion between the lead foil and the active material is decreased so that peeling of the active material layer or the like may occur. On the other hand, if the content of Sn is more than 2% by mass, intergranular corrosion susceptibility is increased so that the lead foil may be easily degraded.
The lead foil preferably contains at least one type (metal) selected from the group consisting of Ca, Ag, and Cu. When any components of Ca, Ag, and Cu are contained in the lead foil, the metal structure of the lead alloy can be made uniform, and the surface state specified in the present embodiment can be easily formed. Furthermore, the content of Ca is preferably more than 0% by mass and 0.1% by mass or less, the content of Ag is preferably more than 0% by mass and 0.05% by mass or less, and the content of Cu is preferably more than 0% by mass and 0.05% by mass or less. If the content of any component exceeds the above upper limit value, the corrosion resistance of the lead foil is decreased. On the other hand, if the contents of Ca, Ag, and Cu are lower than the above lower limit values, lead is easily deformed. Hence, it is difficult to thinly roll the lead foil.
Furthermore, it is preferable that the lead foil contains Bi, and the content of Bi is more than 0% by mass and 0.004% by mass or less. When Bi is contained in the lead foil, the metal structure of the lead alloy can be made uniform, and the surface state specified in the present embodiment can be easily formed. However, if the content of Bi is more than 0.004% by mass, the moldability of the lead foil may be deteriorated. In particular, when the final plate thickness of the lead foil is thin, there is a high possibility that poor processability due to the addition of Bi may become apparent.
The content of each composition of the lead foil is determined by an emission spectroscopic analysis method.
In being subjected to rolling processing, the lead foil according to the present embodiment can be produced by using a rolling roll whose circumferential side surface is roughened in advance. In this case, by polishing the circumferential side surface of the rolling roll with a steel brush, a grindstone having a coarse grain size, or the like, the circumferential side surface can be provided with irregularities satisfying the above contact length X, and the circumferential side surface can be roughened. The polishing may be performed multiple times by changing a polishing pressure. In this case, by gradually reducing the polishing pressure, a groove formed by the polishing can be further provided with a groove in the subsequent polishing, so that the contact length X can be increased. Furthermore, when the circumferential side surface of the rolling roll is sufficiently rough, rolling may be performed without the processing for providing irregularities on the circumferential side surface. When irregularities are provided to the rolling roll, it is preferable to use, for the rolling roll, a hard material such as a chrome-plated product so that the roll lines of the rolling roll are not crushed. The lead foil rolled by the rolling roll may further be provided with irregularities by using a steel brush or the like. In this case, irregularities satisfying the above contact length X may be provided by brushing with a steel brush in directions of 0°, 45°, and 90° with respect to the rolling direction.
Modifications
Although the present invention has been described above with reference to specific embodiments, these descriptions are not intended to limit the invention. Another embodiment of the present invention, including various modifications along with the disclosed embodiments, will also be apparent to those skilled in the art with reference to the descriptions of the present invention. Therefore, it should be understood that the embodiments of the invention described in the claims also cover embodiments including, alone or in combination, these modifications described in the present description.
For example, in the above embodiments, the contact length X is specified for the back surface of the lead foil, but the present invention is not limited to such an example. For example, not only the back surface, but also the front surface of the lead foil may have the same configuration as the back surface.
Examples performed by the present inventors will be described. In the Examples, a rolling roll plated with chromium was polished with a grindstone having a coarse grain size. In the polishing, the grindstone had a grain size of up to #80. In finishing with a grain size of #80, polishing was performed at a polishing pressure of 0.04 to 0.05 MPa, and then polishing was further performed at a weak polishing pressure of 0.02 to 0.03 MPa. Then, a lead foil was produced by subjecting to rolling processing using the rolling roll. For the produced lead foil, the contact length X was measured by surface roughness measurement with a stylus, and the thickness of the lead foil was measured.
In addition, as a comparison, the lead foils were similarly rolled under the condition of using a rolling roll whose circumferential side surface has the contact length X of less than 150 μm and under the condition of increasing the content of Bi. The contact lengths X and the thicknesses of the produced lead foils were measured.
In Examples 1 to 11 and 17 to 19 and Comparative Examples 1 and 2, an ingot having a thickness of 8 mm was rolled until the thickness became 0.25 mm. In Examples 12 to 16, an ingot having a thickness of 8 mm was rolled until the thickness became 0.10 mm. The reduction was set to 0.4 mm/pass or more.
In the Examples, the produced lead foils were further subjected to a constant potential test to evaluate a penetration distance of sulfuric acid. In the test, the produced lead foil was bonded to an acrylonitrile butadiene styrene (ABS) resin plate using an epoxy adhesive, which was subjected to the constant potential test. For the epoxy adhesive, a bisphenol A type epoxy resin and a curing agent of an acid anhydride were used. In the constant potential test, Hg/Hg2SO4 was used as a reference electrode, and the potential was held at 1350 mV. The constant potential test was performed in an environment of 60° C. for 4 weeks. The distance at which sulfuric acid infiltrated the interface between the ABS resin and the lead foil was measured by EPMA analysis of the cross section.
As a result of the Examples, the test results of the alloy components of the lead foils, the contact lengths X, the thicknesses of the foils, and the sulfuric acid penetration distances are shown in Table 1. In Table 1, the case where the sulfuric acid penetration distance, as the test result of the sulfuric acid penetration distance, is 5 mm or less is indicated as “⊙(Excellent)”, the case where the sulfuric acid penetration distance is 10 mm or less is indicated as “∘(Good)”, and the case where the sulfuric acid penetration distance is more than 10 mm is indicated as “× (Poor)”.
In Examples 1 to 19, the contact lengths X were 150 μm or more and 1800 μm or less (i.e., between 150 μm and 1800 μm, inclusive), and the penetration distances of sulfuric acid were 10 mm or less, or 5 mm or less, as shown in Table 1, and satisfactory results were obtained. On the other hand, in Comparative Examples 1 and 2, the contact lengths X were as short as less than 150 μm, and the penetration distances of sulfuric acid were also more than 10 mm. This is because the contact lengths X, that is, the lengths of the penetration routes of sulfuric acid, were short. In addition, in Comparative Example 3, the amount of Bi was large. As a result, the moldability was poor, and edge cracking occurred at an intermediate plate thickness to the final finished thickness, and therefore the rolling was interrupted. In Comparative Example 3, satisfactory results were obtained without cracking up to the intermediate plate thickness to the final finished thickness. From the above results, it has been confirmed that penetration of sulfuric acid can be delayed by increasing the contact length X as in the above embodiments, and therefore peeling of the lead foil from the substrate can be suppressed.
The following is a list of reference signs used in this specification and in the drawings.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2021-071371 | Apr 2021 | JP | national |
This application is a continuation of PCT Application No. PCT/JP2022/011073, filed Mar. 11, 2022, the disclosure of which is incorporated herein in its entirety by reference.
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/JP2022/011073 | Mar 2022 | US |
| Child | 18489509 | US |
