JPH0747646A - Polyester composite film for lamination of metal - Google Patents

Abstract

PURPOSE:To provide a polyester composite film for the lamination of a metal excellent in deformation properties, impact resistance, close adhesiveness and heat resistance at the time of can manufacturing, not generating the sticking of a punch or the mark of a feed pin and excellent in flavor resistance. CONSTITUTION:A polyester composite film consists of layers A, B, and C and the layer A is composed of PET or polyethylene terephthalate isophthalate with an m.p. of 210 deg.C or higher and the layer B is composed of a polyester with Tg of 40 deg.C or lower containing 50mol% or more of a terephthalic acid residue, 5-50mol% of a 10C aliphatic dicarboxylic acid residue and 50mol% or more of 1,4-butane diol and the layer C is composed of a polyester with an m.p. of 180-230 deg.C.

Description

Detailed Description of the Invention

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a polyester composite film for laminating metal, and more particularly, for obtaining a metal can having a long can wall (for example, beer can, carbonated beverage can, juice can, aerosol can, etc.). The present invention relates to a polyester composite film suitable as a constituent material for a laminated steel sheet.

[0002]

2. Description of the Related Art Conventionally, coating is applied to a metal can to prevent a metallic odor from migrating to the contents and the inner surface of the metal can from being corroded by the contents.
For the purpose of process simplification, improvement of hygiene, pollution prevention, etc., without using an organic solvent, tin, tin-free steel, after laminating the polyester film on a metal plate such as aluminum by heating and pressure bonding, The method of making cans by drawing is being studied.

For example, JP-B-57-23584, JP-B-59-34580 and JP-B-62-61.
The technical contents are disclosed in Japanese Patent No. 427 and the like. However, in the art, when the film is laminated and sufficiently adhered to the steel plate at a temperature equal to or higher than the melting point of the polymer constituting the film, the shock is generated during the can manufacturing process, that is, the shock that hits the stopper at a high speed causes local damage to the bottom of the can. Film tears (cracks) occur. In order to avoid such drawbacks, when the flexibility of the film is improved and deformation resistance and impact resistance are to be secured, the film adheres to the punch due to the processing heat generated by the die and punch in the can making process, and as a result, The film on the can wall often tears and tears. further,
Traces of transport pins are likely to be left during transport in the heat treatment process after the can manufacturing process. That is, various problems occur due to insufficient heat resistance. Further, the polyester having improved flexibility has a drawback that the property of adsorbing the aroma component in the can filling is deteriorated, that is, the flavor resistance is poor. From the above, it is not satisfactory as the protective layer for the inner layer of the metal can.

In order to avoid such a drawback, Japanese Patent Laid-Open No. 2-8
Japanese Patent No. 1630 discloses a method of using a two-kind two-layer composite polyester film. However, in terms of the balance between moldability and heat resistance, it has been difficult to achieve a level that satisfies market requirements.

[0005]

SUMMARY OF THE INVENTION The present invention has been made in view of the above circumstances, and it is possible to secure the deformability, the impact resistance and the adhesion at the time of the can manufacturing process, and it is also excellent in heat resistance. Punch adhesion during processing and traces of transport pins do not occur, and moreover,
Provided is a polyester composite film for metal laminating, which has good flavor resistance.

[0006]

The present invention is directed to an A layer, a B layer,
A polyester composite film comprising a C layer, wherein the A layer is made of polyethylene terephthalate or a copolymer of polyethylene terephthalate and isophthalate having a melting point of 210 ° C. or higher, and the B layer is 50 mol% or more of all dicarboxylic acid components. Is a terephthalic acid residue, 5 to 50 mol% contains an aliphatic dicarboxylic acid residue having 10 or more carbon atoms, and 50 mol% or more of all alcohol components is a 1,4 butanediol residue. The melting point of the C layer is 180 to 230 ° C.
Is a polyester composite film for metal laminating.

The polyester resin constituting the layer A in the present invention must be polyethylene terephthalate or a copolymer of polyethylene terephthalate and isophthalate having a melting point of 210 ° C. or higher. There is no problem that such a polyester resin contains a diethylene glycol residue produced as a by-product in the manufacturing process. Further, if it is 5 mol% or less within the above melting point range, other copolymerization components may be contained, but it is preferable not to contain other copolymerization components from the viewpoint of flavor resistance. From the viewpoint of flavor resistance, it is better that the content of diethylene glycol residue is as low as possible. The polyester resin must have a melting point of 210 ° C. or higher. 220 degreeC or more is preferable. If the temperature is less than 210 ° C, heat resistance is low and punch sticking occurs during can manufacturing, which lowers the operability of the can manufacturing process and causes problems such as tearing of the film on the can wall and tearing. Not preferable.

The polyester resin may be polyethylene terephthalate, but a copolymer of polyethylene terephthalate and isophthalate having a melting point of 220 to 250 ° C. is particularly preferable from the viewpoint of deformability and impact resistance. The copolymerization ratio of isophthalate varies depending on the amount of diethylene glycol residue produced as a by-product in the polyester production process, but is generally in the range of 3 to 15 mol%. A layer thickness is 1 to 20
μm is preferable, and 2 to 15 μm is more preferable. If it is less than 1 μm, the effect of improving heat resistance and flavor resistance is not sufficient, which is not preferable. On the contrary, if it exceeds 20 μm, the effect of improving the heat resistance and the flavor resistance is saturated, and the deformability and the impact resistance are deteriorated, which is not preferable.

In the polyester resin constituting the layer B in the present invention, 50 mol% or more of all acid components are terephthalic acid residues, 5 to 50 mol% are aliphatic dicarboxylic acid residues having 10 or more carbon atoms, and all alcohols. 50 mol% or more of the ingredients are 1,
It must contain a 4-butanediol residue and have a glass transition point of 40 ° C. or lower. When the content of terephthalic acid is less than 50 mol%, heat resistance becomes insufficient, which is not preferable. Examples of the aliphatic dicarboxylic acid having 10 or more carbon atoms include sebacic acid, eicoic acid, dodecanedicarboxylic acid, dimer acid and the like. The dimer acid is obtained by a dimerization reaction of a higher unsaturated fatty acid such as oleic acid, and usually has an unsaturated bond in the molecule, but those having hydrogenation to reduce the degree of unsaturation can also be used. Hydrogenation is more preferable because heat resistance and flexibility are improved. Further, in the course of the dimerization reaction, a linear branched structure, an alicyclic structure, and an aromatic nucleus structure are produced, but the structure and amount thereof are not particularly limited. An aliphatic dicarboxylic acid residue having a carbon number of less than 10 is not preferable because it does not provide sufficient deformability and impact resistance. The content of the aliphatic dicarboxylic acid residue needs to be 5 to 50 mol% in all the acid components. When it is less than 5 mol%, the impartation of deformability and impact resistance becomes insufficient, which is not preferable. On the contrary, if it exceeds 50 mol%, the deformability and the impact resistance are saturated, and the heat resistance is lowered, which is not preferable.

The polyester resin constituting the B layer is not particularly limited to contain carboxylic acid residues other than terephthalic acid and an aliphatic dicarboxylic acid having 10 or more carbon atoms as an acid component as long as the above range is satisfied. Also, carbon number 1
The number of aliphatic dicarboxylic acid residues of 0 or more may be one,
You may use 2 or more types together. The polyester resin constituting the layer B contains 1,4% or more of all alcohol components in an amount of 50 mol% or more.
Must be a butanediol residue. When it is less than 50 mol%, the crystallinity of the resin is lowered and the handleability of the resin is deteriorated, which is not preferable. It is preferable that 90 mol% or more is 1,4 butanediol residue. Other glycol components include ethylene glycol, diethylene glycol, propylene glycol, neopentyl glycol,
1,4 cyclohexanedimethanol and the like,
It is a preferred practice response that the total amount is 1,4 butanediol residues. The polyester resin that constitutes the B layer is
The glass transition point needs to be 40 ° C. or lower. 30 ° C or lower is more preferable. If the glass transition point exceeds 40 ° C., the deformability and impact resistance are not sufficiently imparted, which is not preferable.

The composition of the polyester resin constituting the layer B can be arbitrarily set within the above range. The thickness of the layer B is preferably 3 to 60 μm. 5-40μ
m is more preferred. If it is less than 3 μm, the imparting of deformability and impact resistance becomes insufficient, which is not preferable. Conversely, 60 μm
If it exceeds the range, the impartation of deformability and impact resistance is saturated, and the heat resistance is reduced, which is not preferable. Also, it is disadvantageous in terms of cost.

The polyester resin forming the C layer must have a melting point of 180 to 230 ° C. Melting point 230 ° C
When it exceeds the above range, the adhesion during heat lamination with a metal plate is deteriorated, and film breakage (cracks) whose melting point is localized film peeling is likely to occur in the can wall portion during the can manufacturing process, which is not preferable. On the other hand, if the temperature is lower than 180 ° C., the adhesion is improved, but the heat resistance is lowered, and wrinkles are liable to be formed during the heat treatment after the can making process, and the commercial value as the metal can inner surface protective layer is not preferable.

The structure of the polyester resin is not limited as long as it has a melting point within the above range, but copolymer polyethylene terephthalate is preferable from the viewpoint of cost. The copolymerization component may be an acid component and an alcohol component. Examples of the acid component include aromatic dicarboxylic acids such as isophthalic acid, phthalic acid and naphthalene dicarboxylic acid, adipic acid, azelaic acid, sebacic acid, decane dicarboxylic acid, dodecane dicarboxylic acid, dimer acid and other aliphatic dicarboxylic acids, cyclohexanedicarboxylic acid. Alicyclic dicarboxylic acids such as and the like, and alcohol components include propanediol,
Examples thereof include aliphatic diols such as butanediol, hexanediol and neopentyl glycol, alicyclic diols such as cyclohexanedimethanol, and ether bond-containing diols such as diethylene glycol, triethylene glycol and polyethylene glycol. These may be used alone or in combination of two or more. The polyester resin is preferably non-quality from the viewpoint of adhesion. The thickness of the C layer is preferably 1 to 15 μm. 2-10 micrometers is more preferable. 2-10 micrometers is more preferable. If it is less than 1 μm, the adhesion to the metal plate becomes insufficient, which is not preferable. On the other hand, when the thickness exceeds 15 μm, the adhesion to the metal plate is saturated, and the deformability and impact resistance decrease, which is not preferable.

It is preferable that each of the polyester resins constituting the layers A, B and C has an intrinsic viscosity of 0.5 or more. It is more preferably 0.7 or more. Further, the polyester resin constituting each layer may be one type, or two or more types may be blended and used. Further, these polyester resins may contain antioxidants, heat stabilizers, ultraviolet absorbers, plasticizers, pigments, antistatic agents, lubricants, crystal nucleating agents, lubricants composed of inorganic or organic particles, etc., if necessary. There is no limitation in blending. The method for producing the polyester resin described above is not particularly limited, and any one produced by a transesterification method or a direct polymerization method can be used. Also,
It may be produced by a solid phase polymerization method to increase the molecular weight. The polyester resin constituting the layer A is a polyester resin having a low oligomer content produced by a reduced pressure solid phase polymerization method from the viewpoint of reducing the precipitation of oligomers from the polyester resin in the retort treatment after filling the can with contents. Is a particularly preferred embodiment.

As described above, the composite film of the present invention is
It does not matter whether it is an unstretched film or a stretched film as long as it is composed of a layer, a B layer and a C layer in this order. The film having the constitution is preferably produced by a multi-layer extrusion method. Uniaxial stretching and 2 in case of stretched film
Any of axial stretching may be used, but a biaxially stretched film is preferable because of its isotropic property. The manufacturing method of the composite film is not limited at all. For example, in the case of a stretched film, either the T-die method or the tubular method can be applied. When the composite polyester film of the present invention is used for metal laminating, it is necessary to use the surface of the C layer as the metal plate side. The laminating method is not particularly limited, but a method in which a composite polyester film is pressure-bonded to a metal plate heated by an electric current method and heat-bonded is the most preferable embodiment.

The present invention will be described below based on examples.
The measuring method used in the examples is as follows. (1) Melting point (Tm), glass transition point (Tg) Obtained using a differential scanning calorimeter. Sample at 300 ° C
After heating and melting for 5 minutes at 10mg
When the temperature was raised at a heating rate of 10 ° C./min, the specific heat change due to the transition from the glass state to the rubber state was read and this temperature was taken as the glass transition point (Tg). In addition, the endothermic peak temperature based on crystal melting was defined as the melting point (Tm).

(2) Adhesiveness The composite polyester film and the tin plate having a thickness of 0.29 mm are overlapped between the metal roll and the rubber roll heated to 230 ° C. (the surface of the C layer of the composite polyester is brought into contact with the tin plate), and the pressure is applied. It was passed at 20 kg / cm. The adhesive strength (laminate strength) of the laminated film and tin product after passing was measured by Tensilon. ◯: Laminate strength is 200 g / cm or more ×: Laminate strength is less than 200 g / cm

(3) Stick temperature The temperature at which the resistance of the metal film heated to a predetermined temperature is brought into contact with the film surface of the laminated film laminated on the tin plate by the method of (2), and the resistance is rapidly increased by adhesion by hand. Measure. The stick temperature was evaluated at 5 ° C pitch and finally at 1 ° C pitch. If the stick temperature is less than 80 ° C, sticking of the punch will occur during the can making process and the operability of the can will be reduced, which is not preferable.

(4) Heat resistance A laminate film laminated on a tin plate by the method of (2) is cut into 5 cm × 5 cm, and the film surface is
After the weight of 100 g was placed and heated at 200 ° C. for 5 minutes, the generation state of traces of the weight steel was visually evaluated.

(5) Impact resistance On the film surface of the laminated film laminated on the tin plate by the method of (2), the tip diameter is 4 mm and the weight is 0.4 kg.
The weight was dropped vertically from a height of 30 cm and deformed to make a model of a can. The can model laminating film is 220
After heat treatment at 10 ° C for 10 minutes, the retort was modeled by placing it in a water-filled autoclave and heating at 120 ° C for 30 minutes. On the deformed portion of the canned model of the retort model-treated laminated film, a weight having a flat bottom and a weight of 0.4 kg was vertically dropped from a tin plate side from a height of 24 cm to give an impact. A vinyl chloride pipe was bonded to the film side of the laminated film which was shocked with an adhesive, 1% saline was put into this, and an electrode was inserted. A voltage of 6 V was applied for 30 seconds after the tin plate was used as an anode. Current value (m
A) was measured. The average value of 10 measurements was displayed.
It is preferably 0.2 mA or less.

(6) Wrinkles after heat treatment The laminated film laminated on the tin plate by the method of (2) was press-molded with a press at a pressure of 100 kg / cm ² to obtain a cup. After the cup was heated at 200 ° C. for 5 minutes, the state of wrinkling of the film was visually evaluated.

(7) Flavor resistance A 10 cm square film is three-way sealed with an impulse sealer with the A layer side as the inner surface. The three-way seal bag is filled with 30 cc of d-limonene, and the opening is sealed with an impulse sealer. The sealed bag is allowed to stand in a thermostatic chamber at 40 ° C. for 10 days to adsorb d-limonene. After the suction bag was opened and d-limonene was discharged, the unsealed film was cut into a piece of 4 cm square, and d-
Clean the limonene with Kimwipe and measure the weight W1 of the film. After vacuum drying the film at 60 ° C. for 24 hours, the weight W ₂ of the film is measured again. d-
The amount of limonene adsorbed was calculated by the following formula and expressed in% by weight. Adsorption amount of d-limonene (%) = W ₁ -W ₂ / W ₂ It is practical that the adsorption amount of d-limonene is 2% or less.

Example 1 Spherical zeolite 2 having an average particle size of 3 μm as the A layer resin 2
Terephthalic acid containing 0.2% by weight of Irganox 1330 as a B layer resin, a copolymerized polyester (Tm 245 ° C.) [polyester A] composed of terephthalic acid / isophthalic acid (molar ratio 95/5) containing 000 ppm and ethylene glycol. / 36-carbon dimer acid (molar ratio 9
Copolymerized polyester (0/10) and 1,4 butanediol (Tm204 ° C, Tg4 ° C) [Polyester B]
Copolymerized polyester (Tm2) from terephthalic acid / isophthalic acid (molar ratio 88/12) and ethylene glycol
25 ° C., Tg 72 ° C.) [Polyester C] at a weight ratio of 8: 2, and terephthalic acid / isophthalic acid (molar ratio: 83) containing 2000 ppm of spherical zeolite having an average particle diameter of 3 μm as a C layer resin. / 17) and a copolymerized polyester (Tm2
15 ° C.) [Polyester D] is melted by separate extruders, the melts are combined in the die in the order of A / B / C layers, and then extruded onto a cooling drum to be cooled to a total thickness of 3
An unstretched film having a thickness of 2 μm (A layer thickness 12 μm, B layer thickness 15 μm, C layer thickness 5 μm) was obtained. Table 1 shows the characteristics of the obtained film and the laminated film with the tin plate (the layer C side is laminated, and all the following Examples and Comparative Examples are layer C side). The composite film obtained in this example is excellent in all the properties of adhesiveness, canning operability, heat resistance, impact resistance, and flavor resistance, and is highly practical as a metal laminating film. there were.

COMPARATIVE EXAMPLE 1 Instead of polyester A as the A layer resin, a copolymerized polyester (Tm of terephthalic acid / isophthalic acid (molar ratio 80/20) containing 2000 ppm of spherical zeolite having an average particle size of 3 μm (Tm) was used. = 200
C) [Polyester E] The characteristics of the unstretched film and the laminated film with a tin plate obtained by the same method as in Example 1 are shown in Table 1. The composite film obtained in this comparative example had a low stick temperature, poor heat resistance and poor canning operability, and was not practical as a metal laminating film.

COMPARATIVE EXAMPLE 2 Instead of polyester D as the C layer resin, a copolymerized polyester (Tm) of terephthalic acid / isophthalic acid (molar ratio 67/33) containing 2000 ppm of spherical zeolite having an average particle size of 3 μm and ethylene glycol was used. = 170
Table 1 shows the properties of the unstretched film and the laminated film with a tin plate obtained by the same method as in Example 1 except that [Polyester F] was used. The composite film obtained in this Comparative Example had a low heat resistance of the adhesive layer, and wrinkles were generated by heat treatment after lamination, which was not practical as a metal laminating film.

Comparative Example 3 Polybutylene terephthalate (Tm2) was used as the B layer resin.
22 ° C., Tg 42 ° C.) [Polyester G] and Polyester C at a weight ratio of 8: 2 were used, except that an unstretched film and a tin plate obtained by the same method as in Example 1 were used. Table 1 shows the characteristics of the laminated film
Shown in. The film obtained in this Comparative Example was inferior in impact resistance and was not practical as a metal laminating film.

Comparative Example 4 Table 1 shows the properties of the unstretched film and the laminate film obtained by the same method as in Example 1 except that the B layer resin was changed to the same polyester A as the A layer resin. The composite film obtained in this comparative example was inferior in impact resistance and was not practical as a metal laminating film.

Comparative Example 5 Table 1 shows the characteristics of the unstretched film and the laminated film with a tin plate obtained by the same method as in Example 1 except that the polyester D was used in place of the polyester D for the C layer resin. The composite film obtained in this comparative example was inferior in adhesiveness and was not practical as a metal laminating film.

Example 2 A non-stretched film and a laminate film with a tin plate obtained by the same method as in Example 1 except that the polyester A was used in place of the A layer resin and a polyester blend having the same compounding ratio as the B layer resin was used. The characteristics are shown in Table 1. The composite film obtained in this Comparative Example had low heat resistance and inferior flavor resistance, and was not practical as a metal laminating film.

Example 2 As a layer A resin, a copolymerized polyester (Tm 220 ° C.) of terephthalic acid / isophthalic acid (molar ratio 85/15) containing 700 ppm of amorphous silica having an average particle diameter of 2.5 μm and ethylene glycol [Tm 220 ° C.] Polyester H], B
Amorphous silica 70 having an average particle diameter of 2.5 μm as a layer resin
Terephthalic acid / isophthalic acid containing 0 ppm (molar ratio 8
Copolymerized polyester (Tm200 ° C.) [Polyester I] of ethylene glycol (0/20) and ethylene glycol was melted by separate extruders and then extruded on a cooling drum and cooled to obtain an unstretched film. The unstretched film was first stretched 3.3 times at 85 ° C. in the machine direction and then 100 in the transverse direction.
After stretching 3.4 times at ℃, heat set at 170 ℃, total thickness 30μm [A layer thickness 9μm, B layer thickness 18μ
m, C layer thickness 3 μm) to obtain a biaxially stretched film. The properties of the obtained film and the laminated film with the tin plate are shown in Table 1. The composite film obtained in this example was excellent in all properties and was highly practical as a metal laminating film.

Comparative Example 7 A biaxially stretched film and a tin plate obtained in the same manner as in Example 2 except that a blended product of polyester G and polyester H in a weight ratio of 9: 1 was used as the B layer resin. Table 1 shows the characteristics of the laminated film of the above.
The composite film obtained in this comparative example was inferior in impact resistance and was not practical as a metal laminating film.

Comparative Example 8 Table 1 shows the characteristics of the biaxially stretched film obtained by the same method as in Example 2 and the laminated film with a tin plate except that polyester G was used as the B layer resin. The composite film obtained in this Comparative Example was also inferior in impact resistance and was not practical as a metal laminating film.

Comparative Example 9 Table 1 shows the characteristics of the biaxially stretched film obtained by the same method as in Example 2 and the laminated film with a tin plate except that polyester A was used as the C layer resin. The composite film obtained in this comparative example was inferior in adhesiveness and was not practical as a metal laminating film.

Comparative Example 10 A biaxially stretched film and a tin plate obtained by the same method as in Example 2 except that a blended product of polyester B and polyester H in a weight ratio of 9: 1 was used as the A layer resin. Table 1 shows the characteristics of the laminated film of the above.
The composite film obtained in this comparative example was inferior in flavor resistance and was not practical as a metal laminating film.

Comparative Example 11 Properties of a biaxially stretched film obtained by the same method as in Example 2 and a laminated film with a tin plate, except that polyester I was used as the resin for all of the layers A, B and C. Is shown in Table 1. The composite film obtained in this comparative example has a low stick temperature, which is a measure of canning operability,
Moreover, it was inferior in heat resistance and impact resistance and was not practical as a metal laminating film.

Example 3 Spherical silica 200 having an average particle size of 3 μm as the A layer resin
Terephthalic acid / isophthalic acid containing 0 ppm (molar ratio 8
8/12) and a copolymerized polyester (Tm 225 ° C.) from ethylene glycol, a terephthalic acid / sebacic acid (molar ratio 80/20) as layer B resin and a polyester (Tm / 95 ° C., Tg 10) from 1,4 butanediol.
C.) and polyester C in a weight ratio of 9: 1, and using polyester I as the C layer resin in the same manner as in Example 1 to obtain a total thickness of 32 .mu.m (A layer 9 .mu.m).
m, B layer 20 μm, C layer 3 μm) to obtain an unstretched film. The properties of the obtained film and the laminated film with the tin plate are shown in Table 1. The composite film obtained in this example was excellent in all properties and was highly practical as a metal laminating film.

Example 4 Polyester H was used as the layer A resin, and terephthalic acid / dodecanedicarboxylic acid (molar ratio 89/1 was used as the layer B resin.
A copolymerized polyester (Tm 205 ° C., Tg 18 ° C.) of 1) and 1,4 butanediol was used, and polyester I was used as the C layer resin.
A biaxially stretched film having a thickness of 9 μm (A layer 9 μm, B layer 20 μm, C layer 3 μm) was obtained. The properties of the obtained film and the laminated film with the tin plate are shown in Table 1. The composite film obtained in this example was excellent in all properties and was highly practical as a metal laminating film.

Example 5 Polyethylene terephthalate (T) having an intrinsic viscosity of 1.00 containing 2000 ppm of spherical cross-linked polymethylmethacrylic resin beads having an average particle diameter of 3 μm was used as the A layer resin.
m254 ° C.), a blended product of polyester B and polyester C as a B layer resin in a weight ratio of 9: 1, and polyester D as a C layer resin were prepared in the same manner as in Example 1 to give a total thickness of 32 μm. An unstretched film of (A layer 6 μm, B layer 23 μm, C layer 3 μm) was obtained. The properties of the obtained film and the laminated film with the tin plate are shown in Table 1. The composite film obtained in this example was excellent in all properties and was highly practical as a metal laminating film.

[0039]

EFFECT OF THE INVENTION The polyester composite film for metal laminating of the present invention has a three-layer structure and the characteristics of the polyester resin constituting each layer are controlled within a specific range. When applied to the production of metal cans with long can walls after they have been combined, they have excellent thermal adhesion to metal plates and can processability, and also have excellent heat resistance and can process. It is very useful because it has good operability in the process and has excellent impact resistance and flavor resistance after can making.

[0040]

[Table 1]

 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Saburo Ota 344 Maebata, Kizu, Inuyama City, Aichi Prefecture Inuyama Plant, Toyobo Co., Ltd. (72) Kuniharu Mori 344 Maebata, Kizu, Inuyama City, Aichi Prefecture Toyo Spinning Co., Ltd. Inuyama Plant (72) Inventor Tsutomu Isaka 2-8 Dojimahama, Kita-ku, Osaka Toyobo Co., Ltd. Head Office

Claims (1)

[Claims] 1. A polyester composite film comprising an A layer, a B layer and a C layer, wherein the A layer comprises polyethylene terephthalate having a melting point of 210 ° C. or higher or a copolymer of polyethylene terephthalate and isophthalate, The layer contains terephthalic acid residues in an amount of 50 mol% or more of all dicarboxylic acid components, and aliphatic dicarboxylic acid residues of 5 to 50 mol% in an amount of 10 or more carbon atoms.
Polyester for metal laminating, characterized by comprising a polyester resin having a glass transition point of 40 ° C. or lower having a mol% of 1,4 butanediol residue and a C layer of 180 to 230 ° C. Composite film.