CN114616698A

CN114616698A - Lead-acid battery

Info

Publication number: CN114616698A
Application number: CN202080074956.XA
Authority: CN
Inventors: 立泽正仁; 伊藤悦子; 安藤和成
Original assignee: GS Yuasa International Ltd
Current assignee: GS Yuasa International Ltd
Priority date: 2019-10-28
Filing date: 2020-08-27
Publication date: 2022-06-10
Also published as: JPWO2021084878A1; WO2021084878A1

Abstract

The present invention provides a lead storage battery, comprising: a positive electrode plate, a negative electrode plate, and a separator interposed between the positive electrode plate and the negative electrode plate. The positive electrode plate includes a positive electrode material. The positive electrode material contains an Sb element. The content of the Sb element in the positive electrode material is 0.05 mass% or more. The separator contains a polyolefin and an oil and has an apparent density of 0.46g/cm³Above and less than 0.57g/cm³。

Description

Lead-acid battery

Technical Field

The present invention relates to a lead storage battery.

Background

Lead storage batteries are used in various applications other than vehicle-mounted and industrial applications. A lead-acid battery comprises a positive electrode plate, a negative electrode plate, a separator interposed therebetween, and an electrolyte. Various performances are required for structural elements of lead storage batteries.

Patent document 1 proposes a ribbed separator for a lead-acid battery, which is produced by heating and melting a raw material composition comprising a mixture of 20 to 69 mass% of a polyolefin resin, 80 to 40 mass% of an inorganic powder, and 40 to 240 mass% of a mineral oil based on the blend of the polyolefin resin and the inorganic powder, kneading the mixture, molding the mixture into a sheet having ribs, immersing the sheet in an immersion tank containing an organic solvent capable of dissolving the oil, extracting and removing a part of the oil, and heating and drying the extracted oil, wherein the difference between the oil content in the ribs and the oil content in the base of the separator is 5 mass% or less.

Patent document 2 proposes a lead-acid battery in which both a positive electrode plate and a negative electrode plate are provided with a drawn grid body, the electrode plate having either a positive electrode or a negative electrode is accommodated in a bag-shaped separator made of a polyolefin synthetic resin sheet such as microporous polyethylene, and a plate group in which electrode plates of the other polarity are laminated is provided, a plurality of linear ribs are provided in the vertical direction on a surface facing a positive plate surface of the bag-shaped separator, and a groove rib is provided in the vertical direction on an inner wall parallel to the plate surface of a battery cell in which the plate group is accommodated, and the height of the groove rib is equal to or less than the height of the linear rib.

Patent document 3 proposes a lead battery separator comprising a polyolefin microporous member, the polyolefin microporous member comprising polyethylene, a particulate filler and a plasticizer, the particulate filler being present in an amount of 40 wt% or more, the polyethylene comprising a polymer having a baked string structure containing a plurality of elongated chain crystals and a plurality of folded chain crystals, the string structure having an average repetition or period of 1nm to 150 nm.

Patent document 4 describes a barrier member for a nasal type lead storage battery which is a bulky sheet obtained by wet-papermaking of 30 to 90% by weight of synthetic pulp having a drainage degree of 0.1sec/g to 1.0sec/g, 5 to 30% by weight of a binder capable of bonding at a temperature of the melting point of the synthetic pulp or lower than the decomposition temperature thereof, 5 to 60% by weight of a three-dimensional crimp type eccentric core-sheath or side-by-side type composite fiber, and 40% or less of a reinforcing agent, and which is obtained by wet-papermaking at 200g/cm²The apparent density under load was 0.15g/cm³The following.

Patent document 5 describes a method for manufacturing a sealed lead-acid battery using a Pb — Ca alloy in a positive electrode lattice, wherein antimony or an antimony compound is added to a positive electrode active material, the amount of Sb is 0.005% to 1.0% based on the unit weight of the positive electrode active material, and the time from the injection of the electrolyte to the start of the formation of the electrolytic cell is set to 2 hours or less.

Documents of the prior art

Patent document

Patent document 1 Japanese patent laid-open No. 2001-338631

Patent document 2, Japanese patent laid-open No. 2007-134109

Patent document 3 U.S. patent application publication No. 2017/0294636

Patent document 4 Japanese patent application laid-open No. 6-302313

Patent document 5 Japanese patent application laid-open No. H10-112311

Disclosure of Invention

Lead-acid batteries are required to have high output and long life. In general, in the case where the separator contains oil, oxidative deterioration of the separator can be suppressed, and therefore, is advantageous from the viewpoint of life performance. However, when the separator contains oil, the life performance in the high-temperature deep discharge life test may be deteriorated.

One aspect of the present invention relates to a lead-acid battery including a positive electrode plate, a negative electrode plate, and a separator interposed between the positive electrode plate and the negative electrode plate;

the positive electrode plate includes a positive electrode material,

the positive electrode material contains an element Sb,

the content of the Sb element in the positive electrode material is 0.05 mass% or more,

the separator comprises a polyolefin and an oil, and has an apparent density of 0.46g/cm³Above and less than 0.57g/cm³。

In a lead storage battery, excellent life performance in a high-temperature deep discharge life test can be ensured.

Drawings

Fig. 1 is a partially cutaway perspective view showing an external appearance and an internal structure of a lead-acid battery according to an embodiment of the present invention.

Detailed Description

In a lead-acid battery, generally, the specific gravity of an electrolyte increases due to a charge reaction of an electrode plate group during charging, and the electrolyte having a high specific gravity tends to decrease. However, if the battery is overcharged in the final stage of charging, gas is generated to stir the electrolyte, so that the difference in specific gravity of the electrolyte can be reduced.

Lead storage batteries are also used in an undercharged state called a partial state of charge (PSOC). For example, in an Idle Stop (IS) application such as an Idle Start Stop (ISS) vehicle, a lead storage battery IS used under PSOC. If the lead-acid battery is charged and discharged under PSOC, the battery is less likely to be overcharged, and therefore the electrolyte cannot be stirred. This makes it easy to gradually perform stratification, that is, the specific gravity of the electrolyte in the upper part of the battery decreases and the specific gravity of the electrolyte in the lower part of the battery increases. If the electrolyte is stratified, the negative electrode material in the upper portion of the negative electrode plate is degraded, the binding force in the negative electrode material is reduced, and the capacity is reduced. Thereby, the life performance may be degraded.

A positive electrode material for a lead-acid battery contains lead dioxide having a high oxidizing power as a positive electrode active material. In addition, separators containing polyolefin are often used in lead-acid batteries. The separator including polyolefin is easily deteriorated by being oxidized if it is in contact with the positive electrode material for a long time. In a lead-acid battery, if the separator is oxidized and deteriorated, the flexibility is lowered to cause cracks and short-circuiting, thereby achieving the life.

Separators comprising polyolefins may contain oil as a pore-forming agent, an additive, or the like. If the separator contains oil, the separator containing polyolefin can be inhibited from oxidative deterioration, and is therefore advantageous from the viewpoint of life performance. However, the insulating oil plugs the pores of the separator, and therefore, the electrical resistance of the separator tends to increase. If the resistance of the spacer becomes large, it is difficult to improve the output.

If a low-density spacer is used in a state of containing oil, it is expected that the oxidation resistance of the spacer can be ensured by the oil. Further, if a separator having a low density is used, the diffusibility of the electrolyte can be improved while securing high output, and it is expected that the stratification of the electrolyte is suppressed and the life performance is improved.

However, it is actually clear that if the density of the separator is reduced, oxidation degradation of the separator becomes significant regardless of whether oil is contained, and it may be difficult to ensure high life performance in the high-temperature deep discharge life test.

Then, it can be made clear that: the apparent density of the separator containing polyolefin was 0.46g/cm³Above and less than 0.57g/cm³In the case of (2), if a specific amount of Sb element is contained in the positive electrode material, excellent life performance in a high-temperature deep discharge life test can be obtained.

In view of this finding, a lead-acid battery according to one aspect of the present invention includes a positive electrode plate, a negative electrode plate, and a separator interposed between the positive electrode plate and the negative electrode plate. The positive plate includes a positive electrode material. The positive electrode material contains an Sb element, and the content of the Sb element in the positive electrode material is 0.05 mass% or more. The separator comprises a polyolefin and an oil and has an apparent density of 0.46g/cm³Above and less than 0.57g/cm³。

According to the above aspect of the present invention, by combining the separator having a low apparent density and using the positive electrode material containing the Sb element in a specific content, in the lead storage battery, it is possible to secure a high output and obtain excellent life performance in a high-temperature deep discharge life test. That is, the lead-acid battery can achieve both high output and excellent durability.

The reason why the low-density separator containing polyolefin can obtain excellent life performance in the high-temperature deep discharge life test is considered as follows.

The oxidation degradation of the separator is generally performed by bringing the expanded positive electrode plate surface into direct contact with the base surface of the separator (i.e., the region of the separator facing the positive electrode plate) by repeating charge and discharge of the lead-acid battery (patent document 2 [0013 ]]). In the case where the separator contains oil, oxidation degradation in the basal surface of the separator can be suppressed to some extent. However, if an apparent density of less than 0.57g/cm is used³The separator of (3) may be difficult to suppress oxidation degradation of the separator, regardless of whether the separator contains oil.

If the lead-acid battery is used under PSOC, the stratification is easy to carry out. At an apparent density of 0.57g/cm³In the above case, since ions in the electrolyte are hard to diffuse, stratification is easy to progress. Therefore, charge and discharge reactions are concentrated on the upper portion of the electrode plate, and the capacity is reduced due to deterioration of the negative electrode material on the upper portion of the negative electrode plate, thereby reaching the life. In this case, the lifetime performance is independent of the content of Sb contained in the positive electrode material. In addition, in the high-temperature deep discharge life test, the apparent density of the separator is less than 0.46g/cm³In the case of (3), the oil is easily removed, and oxidation degradation of the polyolefin contained in the separator is easily caused in the region of the separator facing the positive electrode plate.

The apparent density of the separator containing polyolefin was 0.46g/cm³Above and less than 0.57g/cm³In the case of (1), if the content of the Sb element in the positive electrode material is less than 0.05 mass%, the high-temperature deep discharge lifetime test is conductedThe oxidative deterioration of the separator becomes significant. Such oxidation degradation of the separator is not particularly limited as long as it is performed in the region of the separator facing the positive electrode plate, but rather in the vicinity of the lower end of the separator, and the life performance is deteriorated. It has not been known until now that such a problem occurs in a high-temperature deep discharge life test when the apparent density of the separator is in a specific range. It is considered that the oxidation degradation on the separator lower end portion side in the high-temperature deep discharge life test is performed by bringing the detached positive electrode material into contact with the vicinity of the separator lower end portion.

In the above aspect of the present invention, an apparent density of 0.46g/cm is used³Above and less than 0.57g/cm³In the case of the separator of (3), a positive electrode material containing 0.05 mass% or more of Sb element is used. By using such a positive electrode material, softening of the positive electrode material can be suppressed. Thus, it is considered that since the dropping of the positive electrode material can be suppressed, the oxidation degradation of the separator in the vicinity of the lower end portion of the separator can be suppressed. Therefore, high output and excellent life performance in a high-temperature deep discharge life test can be ensured.

The apparent density of the separator may be 0.56g/cm³The following. When the apparent density is in such a range, a higher lifetime performance can be ensured in the high-temperature deep discharge lifetime test.

The oil content in the separator may be 5% by mass or more. In this case, the effect of suppressing the oxidation degradation in the region of the separator facing the positive electrode plate can be improved.

The total pore volume of the positive electrode material may be 0.08cm³More than g. In this case, a higher output of the lead storage battery can be ensured. The total pore volume may be 0.18cm³The ratio of the carbon atoms to the carbon atoms is less than g. In this case, the life performance in the high-temperature deep discharge life test can be further improved.

The positive electrode material may contain α -PbO₂Microcrystalline and beta-PbO₂And (4) microcrystals. In a fully charged lead-acid battery, alpha-PbO₂Crystallite size relative to beta-PbO₂Ratio of crystallites (. alpha. -PbO)₂microcrystalline/beta-PbO₂Crystallite ═ α/β) may be 0.55 or less. In this case, a high initial capacity is easily ensured.

The lead storage battery is generally a liquid type (vented type) lead storage battery. The lead-acid battery IS particularly useful as a lead-acid battery (for example, a lead-acid battery for IS) which can be expected to be charged and discharged under PSOC.

The lead-acid battery for IS less likely to be overcharged, and therefore, scratches are less likely to occur, and the positive electrode material IS likely to soften and fall off. Even when the lead-acid battery according to the above aspect IS used as such a lead-acid battery for IS, the oxidation degradation of the separator accompanying the detachment of the positive electrode material can be suppressed in the high-temperature deep discharge life test.

(description of wording)

(Positive electrode Material)

In the positive electrode plate, the positive electrode material is usually held on a positive electrode current collector. The positive electrode material refers to a portion of the positive electrode plate excluding the positive electrode current collector. The positive electrode plate is attached with a member such as felt or coated paper. Such a member (also referred to as a sticking member) may be used integrally with the positive electrode plate, and is therefore also included in the positive electrode plate. In the case where the positive electrode plate includes the attachment member, the positive electrode material refers to a portion other than the positive electrode current collector and the attachment member.

(Total pore volume in Positive electrode Material)

The total pore volume of the positive electrode material is the sum of the volumes of all pores obtained by the mercury intrusion method.

(apparent Density of separator)

The apparent density of the separator means a value (g/cm) obtained by dividing the mass of the separator by the apparent volume of the separator³). The apparent density of the separator was determined using a sample obtained by cutting the separator. In the case where the separator has a rib, a sample may be cut from the base portion where the rib is not formed.

(polyolefins)

Polyolefin refers to polymers comprising olefins as monomers. Polyolefins may comprise, for example, homopolymers of olefins, copolymers comprising monomeric units of different olefins, and copolymers comprising an olefin and a copolymerizable monomer as monomeric units. The copolymer containing an olefin and a copolymerizable monomer as monomer units contains 1 or 2 or more kinds of olefins as monomer units. The copolymerizable monomer is a polymerizable monomer other than the olefin and copolymerizable with the olefin.

(oil)

The oil is a hydrophobic substance that is liquid at room temperature (a temperature of 20 to 35 ℃) and is separated from water. The oil includes natural oil, mineral oil and synthetic oil.

(fully charged state)

In the present specification, the fully charged state of a lead storage battery is determined according to the definition of JIS D5301: 2019. More specifically, the full charge state is defined as the following state: in a water tank at 25 ℃. + -. 2 ℃, the lead storage battery was charged at a current (A) of 1/10 corresponding to the numerical value of the rated capacity described, and the terminal voltage during charging measured every 15 minutes or the electrolyte density after temperature conversion at 20 ℃ was continuously shown as a constant value in 3-digit significant number for 3 times. The numerical value described as the rated capacity is a numerical value in units of Ah. The unit of the current set on the basis of the numerical value described as the rated capacity is a.

A fully charged lead acid battery is a battery obtained by fully charging a lead acid battery. The full charge of the lead-acid battery may be performed immediately after the formation, or may be performed after a certain period of time after the formation (for example, the lead-acid battery after the formation and during use (preferably, at the initial stage of use) may be fully charged).

In the present specification, a battery at the initial stage of use refers to a battery which does not deteriorate for a long time after the start of use and does not deteriorate substantially.

In the present specification, the pole plate defines a vertical direction with a side on which the lug portion is provided as an upper side and a side opposite to the lug portion as a lower side. In the separator, the side facing the upper side of the electrode plate (i.e., the tab side) is referred to as the upper side of the separator, and the side facing the lower side of the electrode plate is referred to as the lower side of the separator. The up-down direction of the pole plate and the up-down direction of the separator are respectively the same as the up-down direction in the vertical direction of the lead storage battery.

The lead-acid battery according to the embodiment of the present invention will be specifically described below with reference to the drawings. However, the present invention is not limited to the following embodiments.

(spacer)

The apparent density of the separator was 0.46g/cm³The above. When the Sb element content of the positive electrode material is 0.05 mass% or more, the apparent density of the separator is 0.46g/cm³Thus, the high life performance in the high-temperature deep discharge life test can be ensured. From the viewpoint of further ensuring high life performance in the high temperature deep discharge life test, the apparent density of the separator is preferably 0.48g/cm³Above or 0.49g/cm³The above.

The separator has an apparent density of less than 0.57g/cm³It may be 0.56g/cm³The following. By setting the apparent density in such a range, high output and high life performance in a high-temperature deep discharge life test can be obtained. When the Sb element content of the positive electrode material is 0.05 mass% or more, if the apparent density of the separator is 0.56g/cm³Below, 0.57g/cm³Compared with the case (2), the service life performance in the high-temperature deep discharge service life test is obviously improved. That is, when the content of the Sb element in the positive electrode material is 0.05 mass% or more, the apparent density of the separator is 0.56g/cm in the life performance of the high-temperature deep discharge life test³Criticality exists at the time.

The apparent density of the separator may be 0.46g/cm³Above and less than 0.57g/cm³(or 0.56 g/cm)³Below), 0.48g/cm³Above and less than 0.57g/cm³(or 0.56 g/cm)³Below), or 0.49g/cm³Above 0.57g/cm³And less than (or 0.56 g/cm)³Below).

The separator can be obtained, for example, by extrusion-molding a resin composition containing a polymer material (hereinafter also referred to as a base polymer), a pore-forming agent, and a penetrating agent (surfactant) into a sheet shape, and then removing the pore-forming agent. The fine pores may be formed in the matrix of the base polymer by removing at least a portion of the pore-forming agent. The resin composition may further include inorganic particles.

The apparent density of the separator can be adjusted by adjusting at least 1 (typically 2 or more) of the type of pore-forming agent, the amount of the pore-forming agent, the mixing ratio of the base polymer and the pore-forming agent, and the amount of the pore-forming agent removed, for example.

As the base polymer, at least polyolefin can be used. As the base polymer, a polyolefin and other base polymers may be used in combination. The other base polymer is not particularly limited as long as it can be used for a separator of a lead-acid battery. The ratio of the polyolefin to the entire base polymer contained in the separator may be, for example, 50 mass% or more, 80 mass% or more, or 90 mass% or more. The base polymer may be composed of only polyolefin.

Examples of the polyolefin include polyolefins containing at least C_2-3Polymers of olefins as monomer units. As C_2-3The olefin is at least one kind selected from ethylene and propylene. The polyolefin is more preferably polyethylene, polypropylene, or a polyolefin containing C_2-3Copolymers of olefins as monomer units (e.g., ethylene-propylene copolymers). Among the polyolefins, at least polyethylene is preferably used. Polyethylene and other polyolefins may be used in combination.

As the inorganic particles, for example, ceramic particles are preferable. Examples of the ceramic constituting the ceramic particles include at least one of silica, alumina, and titania.

The content of the inorganic particles in the separator is, for example, 40 mass% or more, and may be 50 mass% or more. The content of the inorganic particles is, for example, 80 mass% or less, and may be 75 mass% or less or 70 mass% or less.

The content of the inorganic particles in the separator may be 40 mass% (or 50 mass%) to 80 mass%, 40 mass% (or 50 mass%) to 75 mass%, or 40 mass% (or 50 mass%) to 70 mass%.

Examples of the pore-forming agent include a liquid pore-forming agent and a solid pore-forming agent. As the pore-forming agent, at least oil can be used. The pore-forming agent may be used alone or in combination of two or more. Oils and other pore formers may be used in combination. A liquid pore-forming agent and a solid pore-forming agent may be used in combination. At room temperature (temperature of 20 to 35 ℃), the liquid pore-forming agent may be classified as a liquid pore-forming agent, and the solid pore-forming agent may be classified as a solid pore-forming agent.

The liquid pore-forming agent is preferably mineral oil, synthetic oil, or the like. Examples of the liquid pore-forming agent include paraffin oil and silicone oil. Examples of the solid pore-forming agent include polymer powders.

The pore-forming amount in the separator varies depending on the kind, and therefore cannot be generally defined, but is, for example, 30 parts by mass or more with respect to 100 parts by mass of the base polymer. The pore-forming agent is used in an amount of, for example, 60 parts by mass or less.

The oil content in the separator is, for example, 5 mass% or more. In the high-temperature deep discharge life test, the content of the oil in the separator is preferably 10 mass% or more, more preferably 12 mass% or more, from the viewpoint of suppressing oxidative degradation in the region of the separator facing the positive electrode plate. The content of the oil in the separator is, for example, not more than 20 mass%, preferably not more than 18 mass%.

The content of the oil in the separator may be 5 to 20 mass% (or 18 mass%), 10 to 20 mass% (or 18 mass%), or 12 to 20 mass% (or 18 mass%).

The surfactant as the penetrant may be, for example, either an ionic surfactant or a nonionic surfactant. The surfactant may be used alone or in combination of two or more.

The amount of the penetrating agent in the separator may be, for example, 0.1 part by mass or more and 0.5 part by mass or more per 100 parts by mass of the base polymer. The amount of the impregnation agent is, for example, 10 parts by mass or less, and may be 5 parts by mass or less.

The amount of the penetrating agent in the separator may be 0.1 part by mass (or 0.5 part by mass) to 10 parts by mass, or 0.1 part by mass (0.5 part by mass) to 5 parts by mass, based on 100 parts by mass of the base polymer.

The content of the penetrant in the separator is, for example, 0.01 mass% or more, and may be 0.1 mass% or more. The content of the penetrant is, for example, 5 mass% or less, and may be 10 mass% or less.

The content of the penetrant in the separator may be 0.01 mass% (0.1 mass part) to 10 mass%, or 0.01 mass% (0.1 mass part) to 5 mass%.

The thickness of the spacer is, for example, 0.1mm or more. The thickness of the spacer may be 0.3mm or less. In the case where the spacer is attached with an attaching member (felt, coated paper, or the like), the thickness of the attaching member is included in the thickness of the spacer.

Note that the spacer may have ribs or may not have ribs. The spacer having ribs includes, for example, a base portion and ribs standing from a surface of the base portion. The ribs may be provided only on one side surface of the separator or each base portion, or may be provided on both side surfaces, respectively. The spacer may be sheet-like. Further, the sheet may be bent in a bellows shape to be used as a spacer. The separator may be formed in a bag shape, or either the positive electrode plate or the negative electrode plate may be wrapped in the bag-shaped separator. In the case of using a bag-shaped separator, the lower end portion of the separator is easily oxidized and deteriorated due to contact with the detached positive electrode material. In the above aspect of the present invention, even in the case where such a bag-shaped separator is used, oxidation degradation in the lower end portion of the separator can be suppressed in the high-temperature deep discharge life test.

The ribs may be formed into a sheet when the resin composition is extrusion molded. The ribs may be formed by molding the resin composition into a sheet shape or by removing the pore-forming agent and then pressing the sheet by a roller having grooves corresponding to the respective ribs.

In the case where the spacer has ribs, the height of the ribs may be 0.05mm or more. The height of the rib may be 1.2mm or less. The height of the rib is the height of the portion protruding from the main surface of the base portion (protruding height).

The height of the rib provided in the region of the separator facing the positive electrode plate may be 0.4mm or more. The height of the rib provided in the region of the separator facing the positive electrode plate may be 1.2mm or less.

When the spacer has ribs, the thickness of the base portion is, for example, 0.15mm or more. In this case, the strength of the spacer is easily ensured. From the viewpoint of suppressing the electrical resistance of the separator to be low, the thickness of the base portion is favorably 0.25mm or less, for example, and may be 0.20mm or less.

(analysis of spacer or measurement of dimension)

For analysis of the separator and measurement of the size, a separator taken out from a lead-acid battery at the initial stage of use is used.

The separator taken out of the lead storage battery may be washed and dried before analysis or measurement.

The washing and drying of the separator taken out of the lead storage battery can be performed as follows. The separator taken out from the lead-acid battery was immersed in pure water for 1 hour to remove sulfuric acid in the separator. Then, the separator was taken out from the immersed liquid, and left to stand at 25 ℃. + -. 5 ℃ for 16 hours or more, and dried. When the separator is taken out from the lead-acid battery, the separator is taken out from the lead-acid battery in a fully charged state.

(apparent Density of separator)

The apparent density of the separator can be determined by the following procedure. First, a base portion of the separator was processed into a 100mm × 10mm strip shape so as not to include ribs in a region facing the electrode plate, and a sample (hereinafter referred to as sample a) was prepared. The longitudinal and lateral dimensions and the thickness of the sample a were measured, and the volume of the sample a was determined from the measured values. The apparent density was calculated by measuring the mass of sample a and dividing by the volume. The apparent densities were obtained for a plurality of samples (for example, 20 samples), and the average value was calculated. The obtained average value was taken as the apparent density of the separator.

(oil content in separator)

About 0.5g of sample A was collected and weighed correctly to obtainMass (m) of the sample at the beginning₀). A weighed sample A was placed in a glass beaker of appropriate size, and 50mL of n-hexane was added. Next, ultrasonic waves were applied to the samples for about 30 minutes for each beaker, whereby the oil component contained in sample a was eluted in n-hexane. Next, a sample was taken out from n-hexane, dried at room temperature (temperature of 20 to 35 ℃) in the atmosphere, and then weighed to determine the mass (m) of the sample from which oil had been removed₁). Then, the oil content was calculated from the following equation.

The content (mass%) of oil is (m)₀-m₁)/m₀×100

(content of inorganic particles in the separator)

A part of sample a prepared in the same manner as described above was sampled, and the measurement sample was accurately weighed and placed in a platinum crucible and heated by a bunsen burner until no white smoke was generated. Next, the obtained sample was heated in an electric furnace (550 ℃. + -. 10 ℃ C. in oxygen flow) for about 1 hour to ash, and the ash was weighed. The ratio (percentage) of the mass of the ashed matter to the mass of the sample a was calculated as the content (mass%) of the inorganic particles.

(content of penetrant in separator)

A part of sample a prepared in the same manner as described above was collected, accurately weighed, and dried at room temperature (20 to 35 ℃) in a reduced pressure atmosphere having a pressure lower than atmospheric pressure for 12 hours or more. The dried product was placed in a platinum cell, set in a thermogravimetric apparatus, and heated from room temperature to 800 ℃. + -. 1 ℃ at a heating rate of 10K/min. The weight loss at the time of raising the temperature from room temperature to 250 ℃. + -. 1 ℃ was defined as the mass of the penetrant, and the ratio (percentage) of the mass of the penetrant to the mass of the sample A was calculated as the content (mass%) of the penetrant. As a thermogravimetric apparatus, Q5000IR manufactured by t.a. instruments, inc.

(thickness of the spacer, thickness of the base portion, and height of the rib)

The thickness of the spacer is determined as follows: the thickness of the spacer was measured at 5 points arbitrarily selected in the cross-sectional photograph of the spacer, and the thickness was averaged to obtain the thickness.

The thickness of the base portion is determined as follows: the thickness of the base portion was measured at 5 arbitrarily selected positions in the cross-sectional photograph of the separator, and the thickness was averaged to obtain the thickness.

The height of the ribs can be determined as follows: the height measured at 10 arbitrarily selected positions of the rib from the one main surface of the base portion of the rib was averaged in the sectional photograph of the separator, and the average height was obtained.

(Positive plate)

As the positive electrode plate, a paste type positive electrode plate can be used.

The positive electrode current collector included in the positive electrode plate may be formed by casting lead (Pb) or a lead alloy, or may be formed by processing a lead or lead alloy sheet. Examples of the processing method include drawing and pressing (punching). It is preferable to use a grid-like current collector as the positive electrode current collector because the positive electrode material is easily supported.

The lead alloy used as the positive electrode current collector is preferably a Pb — Ca alloy or a Pb — Ca — Sn alloy in view of corrosion resistance and mechanical strength. The positive electrode collector may have lead alloy layers having different compositions, and the number of the alloy layers may be plural. As the core metal, a Pb-Ca alloy or a Pb-Sb alloy is preferably used.

The positive electrode material contains a positive electrode active material (lead dioxide or lead sulfate) that exhibits capacity by an oxidation-reduction reaction. The positive electrode material contains an Sb element. The positive electrode material may contain other additives (reinforcing materials, etc.) as needed.

In a fully charged state of the lead storage battery, the positive electrode material usually contains α -PbO₂Microcrystalline and beta-PbO₂And (4) microcrystals. At this time, alpha-PbO₂Crystallite size relative to beta-PbO₂The ratio of the crystallites (═ α/β) may be 0.6 or less, 0.55 or less, 0.5 or less, or 0.2 or less. In the case where the α/β ratio is in such a range, active β -PbO₂Since the proportion of fine crystals is relatively large, the initial capacity of the lead-acid battery can be prevented from decreasing, and a high initial capacity can be ensured. The α/β ratio may be 0.05 or more or 0.1 or more. In the high-temperature deep discharge life test, the α/β ratio may be set so that a higher life performance can be easily ensuredIs 0.13 or more, and may be 0.18 or more, or 0.2 or more. The α/β ratio can be controlled by adjusting at least one of the temperature at the time of formation and the specific gravity of the electrolyte at the time of formation, for example.

In a fully charged lead acid battery, the α/β ratio may be 0.05 (or 0.1) to 0.6, 0.13 (or 0.18) to 0.6, 0.2 to 0.6, 0.05 (or 0.1) to 0.55, 0.13 (or 0.18) to 0.55, 0.2 to 0.55, 0.05 (or 0.1) to 0.5, 0.13 (or 0.18) to 0.5, 0.2 to 0.5, 0.05 (or 0.1) to 0.2, or 0.13 (or 0.18) to 0.2.

The content of the Sb element in the positive electrode material is 0.05 mass% or more. By setting the Sb content to 0.05 mass% or more, softening of the positive electrode material can be suppressed, and excellent life performance in a high-temperature deep discharge life test can be ensured. From the viewpoint of easily ensuring a high capacity, the content of the Sb element in the positive electrode material is, for example, 0.6 mass% or less, may be 0.5 mass% or less, and may be 0.3 mass% or less.

The positive electrode plate in which the positive electrode material contains Sb element can be formed by using, for example, an antimony compound (for example, an oxide, a salt, or the like) as an additive.

Examples of the reinforcing material of the additive include fibers (inorganic fibers, organic fibers, and the like). Examples of the resin (or polymer) constituting the organic fiber include at least one selected from acrylic resins, polyolefin resins (polypropylene resins, polyethylene resins, and the like), polyester resins (including polyalkylene acrylates (polyethylene terephthalate and the like)), and celluloses (celluloses, cellulose derivatives (cellulose ethers, cellulose esters, and the like)). Cellulose also includes rayon.

The amount of the reinforcing material in the positive electrode material is, for example, 0.03 mass% or more. The amount of the reinforcing material in the positive electrode material is, for example, 0.5 mass% or less.

The total pore volume of the positive electrode material is, for example, 0.08cm³More than g, also can be 0.09cm³More than g. When the total pore volume is in such a range, the sulfuric acid ion diffusibility is increased, and therefore, it is easy to secure a higher degreeTo output of (c). The total pore volume of the positive electrode material may be, for example, 0.2cm³The ratio of the carbon atoms to the carbon atoms is less than g. The total pore volume of the positive electrode material was 0.18cm³When the amount is less than or equal to/g, the contact between the lead and the lead sulfate particles is easily maintained even when charge and discharge are repeated. Therefore, the effect of suppressing softening and peeling of the positive electrode material by making the content of the Sb element 0.05 mass% or more is further improved. Therefore, in the high-temperature deep discharge life test, it is easier to ensure high life performance.

The total pore volume of the positive electrode material may be 0.08cm³Per g (or 0.09 cm)³/g)～0.2cm³In terms of/g, or 0.08cm³Per g (or 0.09 cm)³/g)～0.18cm³/g。

The unformed paste-type positive electrode plate can be obtained by filling a positive electrode collector with a positive electrode paste, and then curing and drying the positive electrode paste. The positive electrode paste can be prepared by adding water and sulfuric acid to lead powder, an antimony compound, and other additives (reinforcing materials and the like) as needed, and kneading them.

The unformed positive electrode plate is formed into a chemical form, whereby the positive electrode plate can be obtained. The formation can be performed by immersing the electrode plate group including the unformed positive electrode plate in an electrolytic solution containing sulfuric acid in the lead-acid battery cell, and charging the electrode plate group. However, the formation may be performed before the lead-acid battery or the electrode plate group is assembled.

(analysis of the Positive electrode Material or its constituent components)

The analysis of the positive electrode material or its constituent components can be performed using a positive electrode material collected from a positive electrode plate taken out of a fully charged lead-acid battery.

The positive electrode material may be recovered from the positive electrode plate according to the following procedure. First, the fully charged lead-acid battery is disassembled, and the obtained positive electrode plate is washed with water for 3 to 4 hours to remove the electrolyte from the positive electrode plate. The washed positive plate was dried in a thermostatic bath at 60 ℃. + -. 5 ℃ for 5 hours or more. After drying, in the case where the positive electrode plate includes the attachment member, the attachment member is removed from the positive electrode plate by peeling. When the positive electrode plate was observed from the front, the positive electrode material was collected from the vicinity of the center between the top and bottom and the left and right, and a positive electrode material for analysis (hereinafter referred to as sample B) was obtained. Sample B can be pulverized as necessary for analysis.

(amount of reinforcing Material and content of Sb element)

And taking the crushed sample B, and accurately weighing. Next, sample B was added to a mixed solution of an aqueous nitric acid solution (concentration: 25 mass%) and an aqueous tartaric acid solution (concentration: 500g/L) (the mixing ratio (volume ratio) of the aqueous nitric acid solution and the aqueous tartaric acid solution was 7: 2), and the mixture was stirred under heating to dissolve the soluble component. The resulting mixture was filtered using a membrane filter (average pore diameter: 0.45 μm or less). Thus, the reinforcing material contained in the positive electrode material is obtained as a solid on the filter paper. The resulting solid was washed with water and dried. The mass of the dried product was measured. The ratio (percentage) of the mass of the dried product to the mass of sample B was determined. This ratio corresponds to the amount of reinforcing material in the positive electrode material.

The filtrate obtained by filtering the solid matter was diluted with ion-exchanged water as necessary, and the volume was fixed. The filtrate or the diluted filtrate was used as a solution for quantitative determination of Sb, and the emission intensity of Sb in the solution was measured by Inductively Coupled Plasma (ICP) emission spectrometry. Then, the mass of Sb contained in the solution was determined using a calibration curve prepared in advance. The ratio of the mass of Sb to the mass of sample B to be analyzed was determined as the content of Sb element. Analysis by ICP emission spectrometry can be carried out using SPECTRO-ARCOS manufactured by Hitachi High-Tech Science Company.

(Total pore volume of Positive electrode Material)

The content of the sample B was measured using an unpulverized sample B by a mercury porosimeter (Autopore IV9510, manufactured by Shimadzu corporation). The pressure range to be measured is set to 1psia (. apprxeq.6.9 kPa) to 60,000psia (. apprxeq.414 MPa). The pore size distribution is in the range of 3nm to 100 μm.

(alpha/beta ratio)

The α/β ratio can be determined by measuring the X-ray diffraction (XRD) spectrum using the pulverized sample B, from eachPbO₂The intensity ratio of the peaks of the crystallites. In the XRD spectrum, a peak near 25.5 ° 2 θ and a peak near 28.5 ° 2 θ were β -PbO, respectively₂Microcrystalline and alpha-PbO₂Peaks of crystallites. XRD measurement was carried out by using Smart Lab (horizontal goniometer type. theta. -theta., Cu-Ka line) which is a fully automatic multi-purpose X-ray diffraction apparatus manufactured by RIGAKU corporation.

(negative plate)

The negative electrode plate of the lead storage battery is composed of a negative electrode collector and a negative electrode material. In the negative electrode plate, the negative electrode material is a portion of the negative electrode plate other than the negative current collector. In the negative electrode plate, the above-described sticking member may be stuck. In this case, the attachment member is also included in the negative electrode plate. In the case where the negative electrode plate includes the attachment member, the negative electrode material refers to a portion other than the negative electrode current collector and the attachment member.

The negative electrode current collector may be formed by casting lead (Pb) or a lead alloy, or may be formed by processing a lead or lead alloy sheet. Examples of the processing method include drawing and pressing (punching). It is preferable to use a grid-like current collector as the negative electrode current collector because the negative electrode material is easily supported.

The lead alloy used for the negative electrode current collector may be any of a Pb-Sb alloy, a Pb-Ca alloy, and a Pb-Ca-Sn alloy. These lead or lead alloy may further contain at least 1 kind selected from Ba, Ag, Al, Bi, As, Se, Cu, and the like As an additive element.

The negative electrode material contains a negative electrode active material (lead or lead sulfate) that exhibits capacity by oxidation-reduction reaction, and may further contain a shrinkage inhibitor (an organic shrinkage inhibitor or the like), a carbonaceous material (carbon black or the like), barium sulfate, or the like. The negative electrode material may contain other additives (reinforcing materials, etc.) as needed. Examples of the reinforcing material include fibers (inorganic fibers, organic fibers (organic fibers made of the resin described for the reinforcing material of the positive electrode material, and the like)).

The negative electrode active material in a charged state is spongy lead, but an unformed negative electrode plate is generally produced using lead powder.

The negative electrode plate can be formed by filling the negative electrode current collector with the negative electrode paste, aging and drying the paste to produce an unformed negative electrode plate, and then forming the unformed negative electrode plate into a negative electrode plate. The negative electrode paste is prepared by adding water and sulfuric acid to lead powder, an organic shrinkproof agent, and various additives as needed, and kneading them. In the aging step, the non-oxidized negative electrode plate is preferably aged at a temperature higher than room temperature and a high humidity.

The formation can be performed by immersing the electrode group including the non-formed negative electrode plate in an electrolytic solution containing sulfuric acid in the lead-acid storage battery cell, and charging the electrode group. However, the formation may be performed before the lead-acid battery or the electrode plate group is assembled. Spongy lead is generated through formation.

(electrolyte)

The electrolyte is an aqueous solution comprising sulfuric acid. The electrolytic solution may further contain at least one selected from Na ions, Li ions, Mg ions, Al ions, and the like. The electrolyte may be gelled as necessary.

The specific gravity of the electrolyte at 20 ℃ is, for example, 1.10 or more. The specific gravity of the electrolyte at 20 ℃ may be 1.35 or less. These densities are values of the electrolyte for a lead-acid battery that has been fully charged.

Fig. 1 shows an external appearance of an example of a lead-acid battery according to an embodiment of the present invention.

The lead storage battery 1 includes an electrolytic bath 12 for accommodating the electrode plate group 11 and an electrolyte (not shown). The inside of the electrolytic bath 12 is divided into a plurality of battery chambers 14 by partitions 13. Each cell chamber 14 accommodates 1 electrode group 11. The opening of the electrolytic cell 12 is closed by a lid 15 provided with a negative electrode terminal 16 and a positive electrode terminal 17. In the lid 15, each cell chamber is provided with a liquid port plug 18. When replenishing water, the liquid port bolt 18 is removed and the replenishing liquid is replenished. The liquid port plug 18 may have a function of discharging gas generated in the battery chamber 14 to the outside of the battery.

Each of the electrode groups 11 is formed by stacking a plurality of negative electrode plates 2 and positive electrode plates 3 via separators 4. Here, the bag-shaped separator 4 that houses the negative electrode plate 2 is shown, but the form of the separator is not particularly limited. In a battery chamber 14 located at one end of the electrolytic bath 12, negative electrode sheds 6 of the plurality of negative electrode plates 2 connected in parallel are connected to the penetration connector 8, and positive electrode sheds 5 of the plurality of positive electrode plates 3 connected in parallel are connected to the positive electrode post 7. The positive post 7 is connected to a positive terminal 17 outside the cover 15. In the battery chamber 14 located at the other end of the electrolytic bath 12, the negative electrode housing 6 is connected to the negative electrode post 9, and the positive electrode housing 5 is connected to the penetration connector 8. The negative electrode tab 9 is connected to a negative electrode terminal 16 outside the cap 15. The through-connectors 8 are connected in series with the electrode plate groups 11 of the adjacent cell compartments 14 through-holes provided in the partitions 13.

Hereinafter, the evaluation method of each characteristic will be described.

(Life Performance in the high temperature deep discharge life test)

In the present specification, the life performance in the high-temperature deep discharge life test can be evaluated based on the number of cycles of the lifetime in the high-temperature deep discharge life test.

The high-temperature deep discharge life test can be performed by repeating discharge and charge under the following conditions for a lead storage battery having a rated voltage of 12V in a fully charged state. (a) And (c) is carried out in a gas tank environment at 50 +/-2 ℃.

(a) Discharging 1: with I_DDischarge was carried out at a current value of. + -. 1A for 59 seconds. + -.2 seconds (I)_D: current value (A) of 1/3 for 5-hour rate capacity)

(b) Discharging 2: discharge was performed at a current value of 300A + -1A for 1.0 second + -0.2 second

(c) Charging: charging at 14.2V + -0.03V and 100.0A + -0.5A for 60.0 s + -0.3 s

(d) Repeating: the above (a) to (c) were repeated as 1 cycle until the lifetime was reached. In this case, the suspension is carried out for 40 to 48 hours every 3600 cycles. When it was confirmed that the discharge voltage in the test was lower than 7.2V, the life was determined.

(output)

The output of the lead storage battery is measured in accordance with JIS D5301: 2019, 10.3 cold start current (CCA) test, and the terminal voltage at 30 seconds after the start of discharge. The larger the voltage value, the higher the output. More specifically, the output of the lead-acid battery can be measured by the following procedure.

After the completion of full charge, the lead acid battery in a fully charged state was placed in a water tank at 25 ℃. + -. 2 ℃ for 5 hours. Next, the lead storage battery was placed in a cooling chamber at-18 ℃. + -. 1 ℃ until the electrolyte temperature of 1 cell located at the center or in the vicinity thereof became-18 ℃. + -. 1 ℃. After confirming that the electrolyte temperature of the battery is-18 ℃. + -. 1 ℃, the battery is discharged for 30 seconds at a rated cold-start current (CCA) within 2 minutes. The terminal voltage at 30 seconds after the start of discharge was recorded.

The CCA is 1 which is an index indicating the performance of the lead-acid battery, and for example, in the case of a lead-acid battery having a rated voltage of 12V, it means a discharge current at which the terminal voltage after 30 seconds is 7.2V when the lead-acid battery is discharged at a temperature of minus 18 ℃ ± 1 ℃.

(initial Capacity (20 hour rate))

The initial capacity of the lead-acid battery may be determined in accordance with JIS D5301: 2019 at a 20 hour rate capacity test of 10.1. More specifically, the initial capacity of the lead-acid battery can be measured by the following procedure.

After the completion of full charge, the lead acid battery in a fully charged state was placed in a water bath at 25 ℃. + -. 2 ℃ for about 1 hour. The temperature of the electrolyte was confirmed to be 25 ℃. + -. 2 ℃. The lead storage battery was further placed in a 25 ℃. + -. 2 ℃ water tank until the electrolyte temperature of 1 cell located at the center or in the vicinity thereof became 25 ℃. + -. 2 ℃. The discharge was carried out at a current (A) of 20 hours until the terminal voltage of the lead-acid battery decreased to 10.50V. + -. 0.05V, and the discharge duration t (h) at that time was determined. The initial capacity (Ah) is obtained by multiplying the discharge duration (h) by the 20-hour rate current (a).

Examples

The present invention will be specifically described below based on examples and comparative examples, but the present invention is not limited to the following examples.

Lead storage batteries E1-E26 and R1-R18

(1) Production of negative electrode plate

Lead oxide, carbon black, barium sulfate, lignin, a reinforcing material (synthetic resin fiber), water, and sulfuric acid were mixed to prepare a negative electrode paste. The negative electrode paste was filled into the mesh part of a drawn grid made of a Pb-Ca-Sn alloy containing antimony, and the resultant was cured and dried to obtain an unformed negative electrode plate having a width of 100mm, a height of 115mm and a thickness of 1.2 mm. The amounts of carbon black, barium sulfate, lignin and synthetic resin fiber were adjusted to 0.3 mass%, 2.1 mass%, 0.1 mass% and 0.1 mass%, respectively, as measured in a fully charged state of the formed product.

(2) Production of Positive plate

The positive electrode paste was prepared by mixing lead oxide, antimony trioxide, a reinforcing material (synthetic resin fiber), water, and sulfuric acid. At this time, the amount of antimony trioxide added was adjusted so that the Sb element content in the positive electrode material measured in the above-described procedure became the values shown in tables 1 to 3. The amounts of water and sulfuric acid were adjusted so that the total pore volume of the positive electrode material measured in the above-described procedure became values shown in tables 1 to 3. The amount of the reinforcing material in the positive electrode material measured by the above procedure was set to 0.15 mass%. The positive electrode paste was filled into mesh portions of a drawn grid made of a Pb-Ca-Sn alloy containing antimony, and the resultant was cured and dried to obtain an unformed positive electrode plate having a width of 100mm, a height of 115mm and a thickness of 1.6 mm.

(3) Manufacture of spacers

A resin composition comprising polyethylene, silica particles, a paraffin oil as a pore-forming agent, and a penetrating agent is extruded into a sheet form, and then a part of the pore-forming agent is removed. The apparent density of the separator is adjusted by adjusting at least 1 selected from the group consisting of the mixing ratio of polyethylene to silica particles to the pore-forming agent and the amount of the pore-forming agent removed. The penetrant is used in a proportion of 2 parts by mass to 100 parts by mass of polyethylene. Thus, microporous membranes having apparent densities determined in the above-described steps as shown in tables 1 to 3 were produced. In the extrusion molding, a die capable of forming a plurality of ribs in a strip shape is used. Each sheet-like microporous membrane was folded in half to form a bag, and a bag-like separator was obtained.

The composition of the resin composition containing polyethylene, silica particles, pore-forming agent, and penetrating agent can be arbitrarily changed depending on at least 1 selected from the design of the separator, the production conditions, and/or the method of using the lead-acid battery, for example. For example, at least one of the amount of the penetrating agent and the amount of the pore-forming agent removed in the separator may be adjusted as necessary.

On the outer surface of the bag-like separator, a plurality of strip-like mini-ribs having a protrusion height of 0.18mm were provided at intervals of 1mm at both side edges in the width direction of the bag-like separator. In the outer surface of the bag-like separator, a plurality of main ribs in the form of stripes having a projection height of 0.6mm were provided at a pitch of 9.8mm in the region inside the edge portions on both sides where the mini ribs were provided. The total thickness of the spacer was 0.8 mm. The content of the silica particles in the separator was 60 mass%. The total thickness of the separator, the protrusion height of the ribs, the pitch of the ribs, and the content of the silica particles are values obtained for the separator before the production of the lead-acid battery, and are almost the same as values measured in the above-described procedure for the separator taken out from the lead-acid battery after the production.

(4) Production of lead-acid battery

Each of the unformed negative electrode plates was housed in a bag-shaped separator, and for each battery, 7 sheets of the unformed negative electrode plates and 6 sheets of the unformed positive electrode plates were alternately stacked to form an electrode plate group. The tabs of the positive plate and the tabs of the negative plate are welded to the positive electrode shed and the negative electrode shed respectively in a cast-weld busbar (COS) manner. The electrode plate group was inserted into an electrolytic cell made of polypropylene, and an electrolyte was injected into the electrolytic cell to form a liquid lead-acid battery E1 to E26 and R1 to R18, each of which had a rated voltage of 12V and a rated capacity of 30Ah (5-hour rate capacity (capacity at the time of discharge of current (a) of 1/5 expressed in terms of rated capacity)). In the electrolytic cell, 6 electrode plate groups were connected in series.

As the electrolyte, an electrolyte in which aluminum sulfate is dissolved in an aqueous sulfuric acid solution is used. The Al ion concentration of the formed electrolyte was 0.2 mass%. The specific gravity of the electrolyte solution during formation was adjusted within a range of 1.12 to 1.26 so that the α/β ratio in the positive electrode material was a value shown in tables 1 to 3.

The lead-acid battery thus produced was fully charged according to the above procedure and used for the following evaluation.

[ evaluation 1: output ]

The output of the lead acid battery was obtained according to the above procedure.

[ evaluation 2: life Performance in high-temperature deep discharge Life test

The number of cycles until the terminal voltage of the lead-acid battery reached 7.2V was determined according to the above-described procedure.

[ evaluation 3: initial capacity)

The initial capacity of the lead-acid battery was determined according to the above procedure.

The results are shown in tables 1 to 3. Each evaluation is represented by a ratio (%) when the result of the lead storage battery R7 is 100%.

[ Table 1]

As shown in Table 1, the apparent density of the separator was 0.57g/cm³In the case of (2), even when the content of the Sb element in the positive electrode material is changed to 0 mass% to 0.30 mass%, the life performance in the high-temperature deep discharge life test is not changed at all (R7, R9, R11, and R13). In addition, in the positive electrode material of Sb content less than 0.05 mass%, if the separator apparent density is less than 0.57g/cm³The life performance in the high-temperature deep discharge life test is lowered (comparison of R7 with R1 to R6). However, if the content of the Sb element in the positive electrode material is 0.05 mass% or more, the apparent density of the separator is set to 0.46g/cm³Above and less than 0.57g/cm³Thus, the life performance in the high-temperature deep discharge life test is improved (comparison of R8 and R9 with E1 to E6, comparison of R10 and R11 with E7 to E11, and comparison of R12 and R13 with E12 to E16). In this way, when the content of the Sb element in the positive electrode material is 0.05 mass% or more, the influence (behavior) of the apparent density of the separator on the life performance in the high-temperature deep discharge life test is greatly different from that in the case of smaller content. Further, the lead acid batteries E1 to E16 can ensure a high output of 100% or more.

[ Table 2]

As shown in Table 2, the total pore volume of the positive electrode material is preferably 0.08cm from the viewpoint of ensuring higher output³A value of at least one gram, more preferably 0.09cm³More than g. From the viewpoint of ensuring higher life performance in the high-temperature deep discharge life test, the total pore volume of the positive electrode material is preferably 0.18cm³The ratio of the carbon atoms to the carbon atoms is less than g.

[ Table 3]

As shown in table 3, when the α/β ratio in the positive electrode material is 0.55 or less, a higher initial capacity can be secured. In the high-temperature deep discharge life test, the α/β ratio is preferably 0.18 or more or 0.2 or more from the viewpoint of ensuring higher life performance.

Industrial applicability

The lead acid battery according to the above aspect of the present invention IS suitable for, for example, a starting power source for IS applications (lead acid batteries for ISs vehicles, etc.) and various vehicles (automobiles, motorcycles, etc.). Lead storage batteries are preferably used as power sources for industrial power storage devices (e.g., electric vehicles (e.g., forklifts)). These applications are merely examples, and the lead storage battery according to the above aspect of the invention is not limited to these applications.

Description of the symbols

1: lead-acid battery, 2: negative plate, 3: positive plate, 4: spacer, 5: positive electrode shed, 6: negative electrode shed, 7: positive pole, 8: through connector, 9: negative electrode column, 11: pole plate group, 12: electrolytic cell, 13: partition, 14: battery chamber, 15: a cover, 16: negative electrode terminal, 17: positive electrode terminal, 18: liquid mouth bolt

Claims

1. A lead-acid battery is provided with: a positive plate, a negative plate, and a separator interposed between the positive plate and the negative plate;

the positive plate comprises a positive electrode material,

the positive electrode material contains an element Sb,

the separator comprises a polyolefin and an oil and has an apparent density of 0.46g/cm³Above and less than 0.57g/cm³。

2. The lead-acid battery according to claim 1, wherein the apparent density is 0.56g/cm³The following.

3. The lead-acid battery according to claim 1 or 2, wherein the content of the oil in the separator is 5% by mass or more.

4. A lead-acid battery according to any one of claims 1 to 3, wherein the total pore volume of the positive electrode material is 0.08cm³/g～0.18cm³/g。

5. A lead-acid battery according to any one of claims 1 to 4, wherein, in the lead-acid battery in a fully charged state,

the positive electrode material contains alpha-PbO₂Microcrystalline and beta-PbO₂The micro-crystal is formed by the micro-crystal,

the alpha-PbO₂Crystallites relative to the beta-PbO₂The ratio of the crystallites is 0.55 or less.

6. A lead-acid battery according to any one of claims 1 to 5, which is for idling stop.