JP2005056729A - Aluminum laminate material for battery packing - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide an aluminum laminate material for battery packing satisfying forming property, barrier property, content resistant property, and blanching property, and accommodating for diversification of content shapes and a request of high quality. <P>SOLUTION: The aluminum laminate material 1 used for the battery packing comprises a non-oriented polypropylene layer 2 having a thickness of 10-60 μm, an acid-modified polypropylene layer 3 having a thickness of 1-5 μm, a first chemical conversion coating layer 41 having a coating amount of 5-30 mg/m<SP>2</SP>, an inside laminated part 11 formed by successively laminating an aluminum foil layer having a thickness of 10-100 μm, and an outside laminated part 12 arranged on the outside of the aluminum foil layer 10 and formed by laminating a plurality of layers containing an outermost layer 6 made of synthetic resin. The outside laminated part 12 is preferably formed by successively laminating a second chemical conversion coating layer 41 having a coating amount of 5-30 mg/m<SP>2</SP>, an adhesive layer 5 having a thickness of 1-5 μm, and an outermost layer 6 having a thickness of 10-40 μm and made of synthetic resin. <P>COPYRIGHT: (C)2005,JPO&NCIPI

Description

  The present invention relates to an aluminum laminate material excellent in moldability, barrier properties, content resistance and whitening properties as a packaging material for polymer secondary batteries used in electronic devices, electronic components, particularly mobile phones, laptop computers and the like. .

  Conventionally, metal containers have often been used for battery exterior materials. However, electronic devices such as mobile phones and notebook computers have been improved in performance and weight, the weight of batteries used in them has also been reduced, and the thickness and weight have been reduced to make the space as small as possible. Is required. In order to meet such a demand, a lithium ion polymer secondary battery using an electrolytic solution as a gel polymer electrolyte has been developed, and an aluminum laminate material is used as an outer packaging material to reduce the thickness.

  Battery exterior materials are drawn into various sizes depending on the application, and electrodes, separators, and the like are accommodated therein, and a method of sealing three sides is used. Such an aluminum laminate material requires moldability, strength, water vapor barrier properties, content resistance, and the like. If cracks occur in the film or metal foil of the exterior material during drawing, moisture and There have been problems that air permeates and the metal foil is corroded by the electrolytic solution and adversely affects battery performance, and various devices have been made.

For example, conventional battery exterior materials include a boehmite-treated aluminum foil surface (Patent Document 1), an ultraviolet-irradiated film (Patent Document 2), and an acid-modified polyolefin particle and slip on the innermost film. There are those in which an organosol containing an agent is applied (Patent Document 3) and those in which a lubricant such as silicone oil is applied on the innermost film surface (Patent Document 4).
However, none of the above conventional techniques satisfy all of moldability, barrier properties, content resistance and whitening properties. And the aluminum laminate material for battery packaging which can respond to diversification of the contents shape and quality improvement was calculated | required.
JP 2002-298996 A JP 2002-42745 A JP 2001-240113 A JP 2001-176465 A

  The present invention has been made in view of such conventional problems, satisfying all of moldability, barrier properties, content resistance and whitening properties, and can cope with diversification of content shapes and high quality. It is intended to provide an aluminum laminate material for battery packaging.

The present invention is an aluminum laminate material for battery packaging used for battery packaging,
From the inner surface, an unstretched polypropylene layer having a thickness of more than 10 μm and not more than 60 μm, an acid-modified polypropylene layer having a thickness of 1 to 5 μm, a first chemical conversion film layer having a coating amount of 5 to 30 mg / m ² , and a thickness of 10 to 100 μm An inner laminated portion formed by sequentially laminating aluminum foil layers,
An aluminum laminate material for battery packaging, comprising: an outer laminated portion formed by laminating a plurality of layers including an outermost layer made of a synthetic resin, disposed outside the aluminum foil layer. 1).

As described above, the aluminum laminate material for battery packaging of the present invention (hereinafter, simply referred to as “laminate material”) includes the above-mentioned inner laminate portion disposed inside the aluminum foil layer, the unstretched polypropylene layer, and the acid-modified material. It comprises a polypropylene layer and the first chemical conversion film layer. Therefore, the laminate material exhibits very excellent characteristics for battery packaging due to the presence of the inner laminated portion.
That is, very excellent moldability, content resistance, and whitening can be exhibited by a combination of the aluminum foil layer, the first chemical conversion film layer, the acid-modified polypropylene, and the unstretched polypropylene.

  The thickness of the unstretched polypropylene layer located in the innermost layer (inner surface) is best in the range of more than 10 μm and not more than 60 μm from the viewpoints of moldability, content resistance and whitening properties. If this thickness is 10 μm or less, there is a problem that the moldability is deteriorated and cracks are liable to occur. On the other hand, if the thickness exceeds 60 μm, the thickness of the laminate material is required to be reduced. There is a problem of going backwards.

  In addition, the thickness of the acid-modified polypropylene layer is best in the range of 1 to 5 μm in order to improve the content resistance. When the thickness is less than 1 μm, there is a problem that the content resistance is deteriorated. On the other hand, when the thickness exceeds 5 μm, there is a problem from the viewpoint of reducing the thickness as described above.

Moreover, the coating amount of the first chemical conversion coating layer should be in the range of 5 to 30 mg / m ² from the point of adhesion between the aluminum foil layer and the acid-modified polypropylene layer and the resistance to content. Is the best. If it is less than 5 mg / m ² , the aluminum foil layer may be corroded due to the influence of the electrolytic solution. On the other hand, if it exceeds 30 mg / m ² , the film tends to cause cohesive failure during molding. There is.

  The thickness of the aluminum foil layer is best in the range of 10 to 100 μm from the viewpoints of moldability and barrier properties. When this thickness is less than 10 μm, there is a problem that pinholes are likely to occur when the aluminum foil layer itself is produced. On the other hand, when it exceeds 100 μm, the point of thinning is the same as above. There is a problem.

The innermost layer in the laminate material of the present invention uses unstretched polypropylene as described above. That is, a material not subjected to so-called stretching treatment is used. Thereby, the outstanding moldability, content resistance property, and whitening property which were mentioned above can be obtained.
In addition, as the acid in the acid-modified polypropylene layer, for example, an unsaturated carboxylic acid such as acrylic acid, methacrylic acid, maleic acid, maleic anhydride, citraconic anhydride, itaconic acid, itaconic anhydride, or the like may be used. it can.

  As the first chemical conversion coating layer, various treatments such as reactive chromate treatment such as phosphoric acid chromate treatment or chromate chromate treatment, reactive nonchromate treatment such as zirconium treatment, coating type chromate treatment, coating type nonchromate treatment, etc. The chemical conversion film layer formed by the method can be applied.

Moreover, the said outer side laminated part arrange | positioned on the outer side of the said aluminum foil layer is the 2nd chemical conversion film layer whose film adhesion amount is 5-30 mg / m < ² >, the adhesive agent layer of thickness 1-5 micrometers, and thickness 10- It is preferable that the outermost layers made of a synthetic resin of 40 μm are sequentially laminated (Claim 2).
As the outer laminated portion, a laminated structure using various synthetic resins can be applied. In particular, as described above, the second chemical conversion film layer is provided on the outer surface of the aluminum foil layer, and further thereon. It is preferable to provide the outermost layer with the specific thickness after providing the adhesive layer with the specific thickness. Thereby, the adhesiveness of the outermost layer which consists of synthetic resins, and an aluminum foil layer can be improved, and the outstanding moldability can be ensured.

As with the first chemical conversion film layer, the second chemical conversion film layer is formed by various treatment methods such as reactive chromate treatment, reactive nonchromate treatment, coating chromate treatment, and coating nonchromate treatment. A coating layer can be applied. Moreover, when the coating amount of the second chemical conversion coating layer is less than 5 mg / m ² , there is a risk that the adhesiveness between the aluminum foil layer and the adhesive layer may be lowered, while when it exceeds 30 mg / m ^2. However, there is a problem that cohesive failure of the film is likely to occur during molding.

Moreover, as said adhesive bond layer, a polyurethane-type adhesive agent or an epoxy-type adhesive agent etc. are applicable, for example. And the thickness shall be 1-5 micrometers. When the thickness is less than 1 μm, there is a possibility that excellent adhesive strength cannot be obtained. On the other hand, if it exceeds 5 μm, there is a risk of causing cohesive failure.
The thickness of the outermost layer is preferably in the range of 10 to 40 μm from the viewpoint of moldability. If this thickness is less than 10 μm, there is a problem that cracks are likely to occur, whereas if it exceeds 40 μm, there is a problem that it goes against the demand for thinning.

  Moreover, it is preferable that the total thickness of the said aluminum laminated material for battery packaging is 50-200 micrometers. By keeping the total thickness within this range, the moldability, barrier property, content resistance and whitening property can be obtained in a balanced manner. If the total thickness is less than 50 μm, cracks are likely to occur and the barrier properties may be reduced. On the other hand, when it exceeds 200 μm, it is not preferable from the viewpoint of thinning.

Further, the aluminum laminate material for battery packaging preferably has a tensile strength of 120 to 180 N / 15 mm and an elongation of 40 to 150%. In addition, 120-180N / 15mm means that the maximum load (N) when carrying out the tension test of the strip-shaped test piece of 15 mm width is 120-180N. By obtaining such mechanical properties, excellent moldability can be ensured.
When the tensile strength exceeds 180 N / 15 mm and when the elongation is 40% or less, the moldability is lowered, and cracks are likely to occur during molding. On the other hand, when the tensile strength is less than 120 N / 15 mm and when the elongation exceeds 150%, the rigidity after molding may be insufficient.

The aluminum foil layer is made of an aluminum alloy comprising Fe of 1.2 to 1.7% by weight, Si of 0.2% by weight or less, Mn of 0.1% by weight or less, and the balance of inevitable impurities and Al. (Claim 5).
If Fe is less than 1.2% by weight, Si is more than 0.2% by weight, or Mn is more than 0.1% by weight, the tensile strength and elongation in mechanical properties may be reduced. On the other hand, when Fe exceeds 1.7% by weight, a coarse intermetallic compound is generated, which may cause a problem that it is easily cracked.

  The unstretched polypropylene layer preferably has a static friction coefficient of 0.35 or less, and the outermost layer preferably has a static friction coefficient of 0.4 or less. When the static friction coefficient of the unstretched polypropylene layer exceeds 0.35, or when the static friction coefficient of the outermost layer exceeds 0.4, a gap is formed between the processing tool and the aluminum laminate material for battery packaging. There is a risk that cracks may occur because of an increase in resistance. Then, by forming the lower limit of the coefficient of friction of the unstretched polypropylene layer that is the innermost layer rather than the outermost layer, molding into the inner laminated portion that is extremely important for moldability, barrier properties, content resistance and whitening properties The damage at the time can be made smaller than that of the outer laminated portion, and the above excellent properties can be surely expressed.

  The outermost layer is preferably made of any one of polypropylene, polyethylene, polyvinyl chloride, polyester, and nylon (R). By applying these materials as the outermost layer, an aluminum laminate material for battery packaging having the above-described excellent characteristics can be reliably configured.

The unstretched polypropylene layer may be composed of two layers, an extruded layer disposed by an extrusion laminating process and a heat fusion film layer disposed on the surface of the extruded layer by thermal fusion. Preferred (claim 8). That is, as the inner laminated portion, a melted polypropylene is extruded onto the acid-modified polypropylene layer, and this is pasted, and further, an unstretched polypropylene film previously prepared in a film state is heat-sealed thereon. It is preferable that they are formed.
Thereby, the said unstretched polypropylene layer can improve a moldability, barrier property, content resistance property, and whitening property more.

The outermost layer is preferably disposed by a dry laminating process (claim 9).
The dry laminating process is a method in which an adhesive layer is disposed on a substrate and dried to some extent, and a film-like layer is stacked on the adhesive layer and pressure-bonded. As the base material, using an aluminum foil layer provided with a chemical conversion film layer, an adhesive layer is disposed thereon and dried, and then a film-like layer made of a synthetic resin constituting the outermost layer is overlaid, By performing pressure bonding using a roller or the like, the outer laminated portion of the aluminum laminate material for battery packaging can be formed.

(Example 1)
An aluminum laminate material for battery packaging according to an embodiment of the present invention will be described with reference to FIGS.
In this example, 29 types of laminate materials (Examples 1 to 29) were produced as examples of the present invention, and 16 types of laminate materials (Comparative Examples 1 to 16) were produced as comparative examples. Several tests to evaluate were conducted.

  As shown in FIG. 1, an aluminum laminate material 1 for battery packaging of Example 1 is formed by sequentially laminating an unstretched polypropylene layer 2, an acid-modified polypropylene layer 3, a first chemical conversion coating layer 41, and an aluminum foil layer 10 from the inner surface. The inner laminated portion 11 is formed. Moreover, it has the outer side laminated part 12 which laminated | stacked the 2nd chemical conversion film layer 42, the adhesive bond layer 5, and the outermost layer 6 in order on the outer side. And in this Example 1, the extrusion layer 21 arrange | positioned by the extrusion laminating process as the said unstretched polypropylene layer 2, and the heat-fusion film layer 22 arrange | positioned by the heat sealing | fusion on the surface of this extrusion layer 21 It consists of two layers.

Examples 2 to 12, 16 to 29 and Comparative Examples 1 to 10, 13, 14, and 16 are basically laminate materials having the same laminated structure as that of Example 1.
Examples 13 and 15 and Comparative Example 11 differ from Example 1 in that the unstretched polypropylene layer 2 was constituted only by the heat-sealing film layer 22 and no extruded layer was used.
Example 14 and Comparative Example 12 differ from Example 1 in that the unstretched polypropylene layer 2 was constituted by only the extruded layer 21 and no heat-sealing film layer was used.
Comparative Example 15 differs from Example 1 in that the acid-modified polypropylene layer 3 was not used and a dry adhesive layer was used instead.

  In Comparative Examples 1 to 5, there are portions in which the outer laminated portion deviates from the preferred range in the present invention in the configuration of the laminate material, and Comparative Examples 6 to 12 have portions in which the inner laminated portion deviates from the scope of the present invention. There is something. Further, Comparative Examples 13 and 14 are those in which the mechanical properties of the entire laminate material deviate from the preferred range, Comparative Example 15 is different from the scope of the present invention in the configuration of the inner laminated portion, and Comparative Example 16 from the preferred range of the static friction coefficient. It is something that comes off.

Tables 1 and 2 show the material and thickness of each layer constituting each of Examples 1 to 29 and Comparative Examples 1 to 16.
Briefly, as the outermost layer 6, any one of Ny: nylon (R) film, PE: polyethylene film, PVC: polyvinyl chloride film, and PET: polyester film was employed.
As the adhesive layer 5 (dry adhesive), A-based: polyurethane-based adhesive or B-based: epoxy-based adhesive was used.
As the first chemical conversion film layer 41 and the second chemical conversion film layer 42, chemical conversion films prepared by PCr: phosphate chromate treatment, Zr: zirconium treatment, Ti: titanium treatment, PZn: zinc phosphate treatment were used.
As the aluminum foil layer 10, an A material containing Fe: 1.0 wt%, Si: 0.1 wt%, Mn: 0.05 wt%, or Fe: 1.5 wt%, Si: 0.1 One of the B materials containing wt% and Mn: 0.05 wt% was used.
As the acid-modified polypropylene layer 3, maleic acid was used for all.
The extruded layer and the heat-sealing layer were both unstretched polypropylene and represented as PP.

Next, a method for manufacturing the battery packaging aluminum laminate material 1 of Example 1 will be briefly described. First, a chemical conversion treatment step of forming the first chemical conversion coating layer 41 and the second chemical conversion coating layer 42 on the inner side surface and the outer side surface of the aluminum foil layer 10 is performed, and then the outer laminated portion 12 including the outermost layer 6 by dry lamination processing. Is provided.
The dry laminating process includes: an adhesive coating process for applying an adhesive on the second chemical conversion film layer 42; a drying process for drying the adhesive to form the adhesive layer 5; Is performed by performing a dry laminating step of press-bonding the outermost layer 6 to the substrate.

  Further, on the inner surface of the aluminum foil layer 10, a step of forming an acid-modified polypropylene layer 3 by applying an acid-modified polypropylene on the second chemical film 42, and an unstretched layer on the acid-modified polypropylene layer 3. An extrusion laminating step of forming the extruded layer 21 by sequentially extruding polypropylene is performed, and a film made of unstretched polypropylene is disposed on the extruded layer 21 and thermally fused to dispose the thermally fused film 22. The inner lamination part 11 is obtained by performing the fusion process.

  Other examples and comparative examples are produced by the manufacturing method almost the same as that of Example 1, but Examples 13 and 15 and Comparative Example 11 omit the extrusion laminating step, and Example 14 and Comparative Example. 12 is different from the case of Example 1 in that the extrusion laminating step is deleted, and in Comparative Example 15, the step of forming the acid-modified polypropylene layer is deleted and the step of forming the dry adhesive layer is added instead. ing.

In this example, the laminate material of each of the above examples and comparative examples is subjected to a test for measuring its mechanical properties and friction coefficients on both sides, and a test for evaluating formability, barrier property, content resistance property, and whitening property. Went.
<Mechanical properties>
A sample for a tensile test was cut out from the laminate materials of the above Examples and Comparative Examples, and a tensile test and a tensile strength and elongation were measured. The tensile test sample was 15 mm wide and 150 mm long. The measurement results are shown in Tables 3 and 4.

<Friction coefficient>
The friction coefficient was measured by a method of sliding a steel ball having a diameter of 12 mm in a three-point ball type slip tester friction test under a load of 200 g. The measurement results are shown in Tables 3 and 4.

<Moldability>
A 100 mm × 150 mm rectangular sheet was cut out from the laminate material of each of the above Examples and Comparative Examples, and overhanging was performed using a square head mold having a molding height free. The quality of the moldability was judged by the molding depth after molding. As the judgment criteria, the case where the forming depth is 4 mm or more is shown as “Good” by ○, and the case where the forming depth is less than 4 mm is shown as “Poor” in Table 3 and Table 4.

<Barrier properties>
A three-side sealed bag is prepared using the laminate material of each of the above examples and comparative examples, and 3 mg of a solution in which ethyl carbonate, diethyl carbonate, and methylene carbonate are mixed in the same volume is injected therein, and 60 ° C. × 90%. Was stored in the atmosphere for 1 week, and the water content in the solution before and after storage was measured by the Karl Fischer method. Table 3 and Table 4 show that the case where the amount of increase in the amount of water is 50 ppm or less is good as ◯, and the case where it is 50 ppm or more is bad as x.

<Content resistance>
The laminate materials of the above examples and comparative examples were immersed in an electrolytic solution (1 mol of lithium hexafluorophosphate solution) at 60 ° C., and the adhesive strength between the aluminum foil layer 10 and the unstretched polypropylene layer 2 was sometimes increased. Sequentially evaluated. As evaluation criteria, those that were not peeled between the aluminum foil layer 10 and the unstretched polypropylene layer 2 were shown as “Good” as “Good”, and those that were peeled as “Poor” as “Poor” as shown in Tables 3 and 4.

<Whitening>
For the whitening property, using the sample after the overhang processing at the time of the above-described moldability evaluation, the unstretched polypropylene layer 2 that is the innermost layer is enlarged and observed, and cracks reaching the aluminum foil layer 10 are not generated. Table 3 and Table 4 show good circles as good and those with cracks as bad x.

As can be seen from Table 3, for Examples 1 to 29, which are examples of the present invention, the mechanical properties and the coefficient of friction are within appropriate ranges, and the moldability, barrier properties, content resistance properties, The whitening properties were all good.
On the other hand, as can be seen from Table 3, Comparative Examples 1 to 16 were below the reference value in at least one evaluation item, and it was found that the comparative examples 1 to 16 had insufficient performance as an aluminum laminate material for battery packaging.

Next, the usage example which used the said aluminum laminated material 1 for battery packaging for the packaging of a battery is shown.
FIG. 2 shows the appearance of the battery 8 formed using the aluminum laminate material 1 for battery packaging as viewed from three directions. The outer peripheral surface of the battery 8 is covered with the battery packaging aluminum laminate material 1, and the two electrodes 81 protrude from one end.

  FIG. 3 shows a cross-sectional view of the battery 8. As is known from the figure, a battery 8 is formed by covering a laminated body formed by sandwiching a separator 85 with a pair of electrodes 81 from both sides with an aluminum laminate material 1 for battery packaging. And the aluminum laminated material 1 for battery packaging is used so that the unstretched polypropylene layer 2 in Example 1 may be located inside.

  The battery 8 having such a structure is such that the laminate material 1 as a package has excellent mechanical properties and friction coefficient as described above, and is excellent in moldability, barrier properties, content resistance properties, and whitening properties. As a result, the battery has high durability without substantially reducing the original performance of the battery.

Explanatory drawing which shows the structure of the aluminum laminated material for battery packaging in an Example. (A) Top view which shows the external appearance of a battery in an Example, (b) Side view, (c) Front view. Explanatory drawing which shows the cross-sectional structure of the battery in an Example.

Explanation of symbols

DESCRIPTION OF SYMBOLS 1 Aluminum laminated material for battery packaging 10 Aluminum foil layer 11 Inner laminated part 12 Outer laminated part 2 Unstretched polypropylene layer 21 Extrusion layer 22 Heat-fusion film layer 3 Acid-modified polypropylene layer 41 First chemical conversion film layer 42 Second chemical conversion film layer 5 Adhesive layer 6 Outermost layer

Claims (9)

An aluminum laminate material for battery packaging used for battery packaging,
From the inner surface, an unstretched polypropylene layer having a thickness of more than 10 μm and not more than 60 μm, an acid-modified polypropylene layer having a thickness of 1 to 5 μm, a first chemical conversion film layer having a coating amount of 5 to 30 mg / m ² , and a thickness of 10 to 100 μm An inner laminated portion formed by sequentially laminating aluminum foil layers,
An aluminum laminate material for battery packaging, comprising: an outer laminated portion formed by laminating a plurality of layers including an outermost layer made of a synthetic resin, which is disposed outside the aluminum foil layer. In Claim 1, the said outer side laminated part arrange | positioned on the outer side of the said aluminum foil layer is the 2nd chemical conversion film layer whose film adhesion amount is 5-30 mg / m < ² >, the adhesive agent layer of thickness 1-5 micrometers, and thickness An aluminum laminate material for battery packaging, wherein the outermost layer made of a synthetic resin having a thickness of 10 to 40 μm is sequentially laminated.   The aluminum laminate material for battery packaging according to claim 1 or 2, wherein the total thickness is 50 to 200 µm.   The aluminum laminate material for battery packaging according to any one of claims 1 to 3, wherein the tensile strength is 120 to 180 N / 15 mm, and the elongation is 40 to 150%.   5. The aluminum foil layer according to claim 1, wherein the aluminum foil layer has Fe of 1.2 to 1.7 wt%, Si of 0.2 wt% or less, Mn of 0.1 wt% or less, and the balance. An aluminum laminate material for battery packaging, characterized by comprising an aluminum alloy consisting of inevitable impurities and Al.   6. The non-stretched polypropylene layer according to claim 1, wherein the non-stretched polypropylene layer has a static friction coefficient of 0.35 or less, and the outermost layer has a static friction coefficient of 0.4 or less. Aluminum laminate material for battery packaging.   The aluminum laminate material for battery packaging according to any one of claims 1 to 6, wherein the outermost layer is made of any one of polypropylene, polyethylene, polyvinyl chloride, polyester, and nylon (R).   8. The unstretched polypropylene layer according to claim 1, wherein the unstretched polypropylene layer includes an extruded layer disposed by extrusion lamination, and a heat-sealed film layer disposed on the surface of the extruded layer by heat fusion. An aluminum laminate material for battery packaging, characterized by comprising two layers.   The aluminum laminate material for battery packaging according to any one of claims 1 to 8, wherein the outermost layer is disposed by a dry lamination process.

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