JP5493939B2 - White laminated polyester film - Google Patents

Description

  The present invention relates to a white polyester film. In particular, it is related with the polyester film for white excellent in decorating property and workability.

  Polyester films have excellent properties such as mechanical properties, electrical properties, and dimensional stability, so they are used in many fields such as magnetic recording materials, packaging materials, electrical insulating materials, photosensitive materials, drawing materials, and photographic materials. Used as a material film.

  However, since the surface of the oriented polyester film is highly crystallized, it has drawbacks such as poor adhesion to various paints, adhesives, inks and the like. Especially in information recording materials and printing materials that use a biaxially stretched polyester film containing a white pigment to impart whiteness, the use of the final product in label applications, card applications such as magnetic cards and IC cards, etc. For example, labels and cards may be temporarily bent during storage. Furthermore, deformation may occur when the antenna, the chip, the memory, and the electronic member are bonded to each other, and modification processing such as embossing and engraving may be performed. At this time, if the adhesiveness between the base film and the covering (printing ink layer, magnetic recording layer, etc.) is poor, the film peels off at the interface and impairs the appearance of the product, or loses the function as a card. Therefore, studies have been conventionally made to impart adhesiveness to the polyester film surface by various methods.

  On the other hand, various proposals have heretofore been made as methods for improving the adhesion of a polyester film. For example, Patent Document 1 discusses a method using a copolyester, and Patent Document 2 uses a copolyester and a water-soluble polyurethane resin as an easy adhesion layer. Further, Patent Document 3 proposes an optically easy-adhesive polyester film having an easy-adhesive layer containing a polyester resin having a glass transition point of 40 to 100 ° C. and a crosslinking agent in order to prevent scratches.

JP 2008-30475 A JP-A-2005-290354 JP 2003-49011 A

  In particular, when the white film is used as a laminate molding material, the white film may be molded after being printed on an easy-adhesion layer provided on the film surface. Such a molded body is used outdoors and indoors as an IC card, an IC tag, a label, a graphic material, an automobile interior material or exterior material, or a building material member. Under such circumstances, the molded body is expected to be exposed to high temperature and humidity for a long time. Therefore, after molding, it is required to maintain good adhesiveness with the printed layer even in a humid heat environment.

  In general, in order to improve the heat and moisture resistance of the coating film itself, a method of increasing the degree of crosslinking of the coating film and forming an easy-adhesion layer having a high glass transition point is performed. However, such an easy-adhesion layer having a high degree of cross-linking has a hard coating film and lowers molding followability, so that when used as a molding material, the adhesiveness in a wet and heat environment may decrease as a result. .

  On the other hand, when an easy-adhesion layer having a low glass transition point is laminated, moldability is improved, and initial adhesion is improved even after molding. However, since the wet heat resistance of the coating film tends to be lowered, the adhesiveness with the printing layer in a wet heat environment is lowered. For this reason, it has been extremely difficult to obtain a white laminated polyester film having flexibility capable of withstanding the molding process and having heat and moisture resistance.

  An object of the present invention is to solve the above problems. That is, it is an object of the present invention to provide a white laminated polyester film suitable for decorating that is excellent in adhesiveness even in a humid heat environment by highly balancing the trade-off characteristics of flexibility and wet heat resistance of an easily adhesive layer. .

The white laminated polyester film of the present invention that can solve the above-mentioned problems has the following configuration.
A first invention is a laminated polyester film having an easy-adhesion layer on at least one surface of a base film made of a polyester film containing a white pigment and / or inorganic particles, wherein the easy-adhesion layer comprises a polyester-based graft copolymer. And a polyester-based graft copolymer grafted with a polymerizable unsaturated monomer containing an acid anhydride having at least one double bond to a hydrophobic copolymerized polyester resin. A white laminated polyester film having a glass transition point (Tig) of the easy-adhesion layer of 30 ° C to 55 ° C.
In the second invention, the blending ratio of the polyester-based graft copolymer and the polycarbonate-based polyurethane in the easy-adhesion layer is polyester-based graft copolymer / polycarbonate-based polyurethane (mass ratio) = 80/20 to 30/70. And it is the said white lamination | stacking polyester film containing 5-40 mass parts crosslinking agent with respect to 100 mass parts of total amounts of a polyester-type graft copolymer and a polycarbonate-type polyurethane.
3rd invention is the said white laminated polyester film characterized by the said crosslinking agent being a block isocyanate type crosslinking agent.
4th invention is the said white laminated polyester film whose reproduction | regeneration isocyanate group content of the said block isocyanate type crosslinking agent is 3-15 mass%.
5th invention is the said white laminated polyester film whose surface specific resistance value of the said easily bonding layer surface in 25% C and 65% RH is 1 * 10 < ⁶ > -10 < ¹³ > (omega | ohm) / square.

  As for the white laminated polyester film of this invention, the easily bonding layer which has a specific resin structure and a specific glass transition point is laminated | stacked. Therefore, it has good molding followability and good adhesion to the printed layer even in a moist heat resistant environment. Therefore, it is suitable as an information recording material or a printing material, particularly as a base material for an IC card.

(Easily adhesive layer)
The easy-adhesion layer of the present invention will be described in detail.
The present inventor has intensively studied how to satisfy the contradictory properties of flexibility and moisture-heat resistance of the easily adhesive layer. As a result, it has been considered to control the glass transition point as an index for prescribing the flexibility of the easy-adhesion layer, but the resin composition constituting the easy-adhesion layer even if it has the same glass transition temperature The inventors have focused on the fact that the heat-and-moisture resistance changes depending on the structure of the present invention, and have reached the present invention. That is, the easy-adhesion layer of the present invention comprises a polyester-based graft copolymer described later and a polycarbonate-based polyurethane, and the glass transition point (Tig) of the easy-adhesion layer is 30 ° C. to 55 ° C.

  The minimum of the glass transition point (Tig) of the easily bonding layer of this invention is 30 degreeC, Preferably it is 35 degreeC, and an upper limit is 55 degreeC, Preferably it is 50 degreeC. If the glass transition point (Tig) of the easy-adhesion layer is less than 35 ° C., sufficient moisture and heat resistance may not be obtained, and the blocking resistance also decreases. If the glass transition point (Tig) of the easy-adhesion layer exceeds 55 ° C., the flexibility of the easy-adhesion layer tends to decrease, and the moisture and heat resistance after molding may decrease. In order to achieve both the heat and moisture resistance and the moldability, it is desirable to set the glass transition point (Tig) of the easy-adhesion layer in such a very narrow specific range. Even if the polyester component and the polyurethane component each have a glass transition point (Tig) within the above range, when an easy-adhesion layer having a crosslinked structure is laminated together with a crosslinking agent in the film forming step, the glass transition point (Tig) May exceed 38 ° C., and sufficient moldability and adhesion in a heat-and-humidity environment cannot be obtained. In order to maintain the glass transition point (Tig) even if it has a crosslinked structure, an appropriate amount of crosslinking agent, an amount of polyurethane and an amount of polyester-based graft copolymer, and a hydrophobic copolymerizable polyester This can be achieved by setting the mass ratio of the resin and the polymerizable unsaturated monomer to a range described later.

  The glass transition point referred to in the present invention is JIS-K7121 in a state where it is laminated as an easy-adhesion layer in a film forming process, that is, in a state where a polyester-based graft copolymer and a polycarbonate-based polyurethane are crosslinked with a crosslinking agent. The extrapolated glass transition start temperature (Tig) measured by a method based on the above.

(Polyester graft copolymer)
In the present invention, the polyester-based graft copolymer is contained in the easy adhesion layer as described above. The polyester-based graft copolymer is necessary for imparting adhesion to the base film and the printing layer. The polyester-based graft copolymer can form a highly self-crosslinking structure and thus has a good effect on moisture and heat resistance. Furthermore, the polyester-based graft copolymer has an adhesive property between the base film and the easy-adhesion layer. Can be improved. If the polyester-based graft copolymer is not included, the micro-adhesive layer is likely to peel off, resulting in not only the printing layer being chipped, but also a decrease in adhesiveness in a moisture and heat resistant environment. Come on. The polyester-based graft copolymer used in the present invention is a polymerizable unsaturated monomer containing an acid anhydride having at least one double bond in a hydrophobic copolymerized polyester resin from the viewpoint of heat and moisture resistance of an easy-adhesion layer. Is used which is grafted. Hereinafter, the polyester-based graft copolymer used in the present invention will be described.

  The polyester-based graft copolymer contained in the easy-adhesion layer is blended in the range of 5 to 90% by mass with respect to the entire solid content of the easy-adhesion layer in order to impart adhesion between the base film and the easy-adhesion layer. Preferably, it is 30 to 80% by mass.

  In the present invention, “grafting” is to introduce a branched polymer composed of a polymer different from the main chain into the main chain of the main polymer. In the present invention, a polymerizable unsaturated monomer containing an acid anhydride having at least one double bond using a radical initiator in a state where a hydrophobic copolymerizable polyester resin is dissolved in an organic solvent It is preferable to carry out graft polymerization by reacting. The reaction product after completion of the grafting reaction is a hydrophobic copolymerizable polyester resin that has not undergone grafting, in addition to the graft copolymer of the desired hydrophobic copolymerizable polyester and polymerizable unsaturated monomer. And a polymer of the above unsaturated monomer that has not been grafted to the hydrophobic copolymerizable polyester. The polyester-based graft copolymer in the present invention includes not only the above-described polyester-based graft copolymer but also an unreacted hydrophobic copolymerizable polyester, a polymer of an unsaturated monomer that has not been grafted, and the like. Also referred to as reaction mixture.

In the present invention, the acid value of the polyester-based graft copolymer obtained by graft polymerization of a polymerizable unsaturated monomer to a hydrophobic copolymerizable polyester resin is preferably 600 eq / 10 ⁶ g or more. More preferably, it is 1200 eq / 10 ⁶ g or more. When the acid value of the graft copolymer is less than 600 eq / 10 ⁶ g, it cannot be said that the adhesion to the substrate film is sufficient.

  The mass ratio of the hydrophobic copolymerizable polyester resin and the polymerizable unsaturated monomer to obtain a desirable graft copolymer suitable for the purpose of the present invention is polyester / polymerizable unsaturated monomer = The range of 40/60 to 95/5 is desirable, more desirably 55/45 to 93/7, and most desirably 60/40 to 90/10. When the mass ratio of the hydrophobic copolymerizable polyester resin is less than 40% by mass, the glass transition point (Tig) of the obtained easy-adhesion layer is increased, the followability at the time of molding is lowered, and in a moisture and heat resistant environment. In some cases, the adhesiveness of the resin may deteriorate. On the other hand, when the mass ratio of the hydrophobic copolymerizable polyester resin is larger than 95% by mass, blocking tends to occur.

  The graft copolymer is in the form of an organic solvent solution or dispersion, or an aqueous solvent solution or dispersion. In particular, a dispersion of an aqueous solvent, that is, a form of a water-dispersed resin is preferable from the viewpoint of working environment and applicability. Such a water-dispersed resin is usually obtained by graft polymerization of at least one hydrophilic polymerizable unsaturated monomer onto the hydrophobic copolymerizable polyester resin in an organic solvent, followed by water addition and organic It can be obtained by distilling off the solvent.

  The glass transition point (Tig) of the graft copolymer is 70 ° C. or lower, preferably 50 ° C. or lower. By using a graft copolymer having a glass transition point (Tig) of 70 ° C. or less for the graft copolymer-containing layer, it has good followability at the time of molding after the printing layer is laminated, and excellent printing even in a heat and humidity resistant environment. Easy adhesion of layer.

(Hydrophobic copolymerizable polyester resin)
In the present invention, the hydrophobic copolymerizable polyester resin is essentially water-insoluble which does not inherently disperse or dissolve in water. When a polyester resin that is dispersed or dissolved in water is used for graft polymerization, the adhesiveness in a heat-and-moisture resistant environment, which is the object of the present invention, is deteriorated. The composition of the dicarboxylic acid component of this hydrophobic copolymerizable polyester resin is as follows: aromatic dicarboxylic acid 60 to 99.5 mol%, aliphatic dicarboxylic acid and / or alicyclic dicarboxylic acid 0 to 40 mol%, polymerizable unsaturated It is preferable that it is 0.5-10 mol% of dicarboxylic acid containing a double bond. When the aromatic dicarboxylic acid is less than 60 mol%, or when the aliphatic dicarboxylic acid and / or the alicyclic dicarboxylic acid exceeds 40 mol%, the adhesion to the printing layer is lowered.

  Moreover, when the dicarboxylic acid containing a polymerizable unsaturated double bond is less than 0.5 mol%, it becomes difficult to efficiently graft the polymerizable unsaturated monomer to the hydrophobic copolymerizable polyester resin. On the other hand, when the amount exceeds 10 mol%, the viscosity is increased by the grafting reaction, and the uniform progress of the reaction is hindered. More preferably, the aromatic dicarboxylic acid is 70 to 98 mol%, the aliphatic dicarboxylic acid and / or the alicyclic dicarboxylic acid is 0 to 30 mol%, and the dicarboxylic acid containing a polymerizable unsaturated double bond is 2 to 7 mol%. It is.

  Examples of the aromatic dicarboxylic acid include terephthalic acid, isophthalic acid, orthophthalic acid, naphthalenedicarboxylic acid, biphenyldicarboxylic acid and the like. It is preferable not to use a hydrophilic group-containing dicarboxylic acid such as 5-sodium sulfoisophthalic acid because the blocking resistance, which is the object of the present invention, decreases. Examples of the aliphatic dicarboxylic acid include succinic acid, adipic acid, azelaic acid, sebacic acid, dodecanedioic acid, and dimer acid. Examples of the alicyclic dicarboxylic acid include 1,4-cyclohexanedicarboxylic acid, 1, Examples include 3-cyclohexanedicarboxylic acid, 1,2-cyclohexanedicarboxylic acid and acid anhydrides thereof. Examples of dicarboxylic acids containing polymerizable unsaturated double bonds include α, β-unsaturated dicarboxylic acids, fumaric acid, maleic acid, maleic anhydride, itaconic acid, citraconic acid, unsaturated double bonds Examples of the alicyclic dicarboxylic acid to be used include 2,5-norbornene dicarboxylic acid anhydride and tetrahydrophthalic anhydride. Of these, fumaric acid, maleic acid, and 2,5-norbornene dicarboxylic acid are preferred from the viewpoint of polymerizability.

  On the other hand, examples of the glycol component include aliphatic glycols having 2 to 10 carbon atoms and / or alicyclic glycols having 6 to 12 carbon atoms and / or ether bond-containing glycols. Examples of the aliphatic glycol having 2 to 10 carbon atoms include ethylene glycol, 1,2-propylene glycol, 1,3-propanediol, 1,4-butanediol, 1,5-pentanediol, neopentyl glycol, 1,6 -Hexanediol, 3-methyl-1,5-pentanediol, 1,9-nonanediol, 2-ethyl-2-butylpropanediol, and the like. Examples of the alicyclic glycol having 6 to 12 carbon atoms include 1,4-cyclohexanedimethanol.

  Examples of the ether bond-containing glycol include diethylene glycol, triethylene glycol, dipropylene glycol, and glycols obtained by adding ethylene oxide or propylene oxide to two phenolic hydroxyl groups of bisphenols, such as 2,2-bis (4 -Hydroxyethoxyphenyl) propane and the like. Polyethylene glycol, polypropylene glycol, and polytetramethylene glycol may be used as necessary.

  In the hydrophobic copolymerizable polyester resin, 0 to 5 mol% of a trifunctional or higher polycarboxylic acid and / or polyol can be copolymerized. As the trifunctional or higher polycarboxylic acid, (anhydrous) Trimellitic acid, (anhydrous) pyromellitic acid, (anhydrous) benzophenone tetracarboxylic acid, trimesic acid, ethylene glycol bis (anhydro trimellitate), glycerol tris (anhydro trimellitate) and the like are used. On the other hand, glycerin, trimethylolethane, trimethylolpropane, pentaerythritol and the like are used as the trifunctional or higher functional polyol. The tri- or higher functional polycarboxylic acid and / or polyol is copolymerized in the range of 0 to 5 mol%, preferably 0 to 3 mol% with respect to the total acid component or the total glycol component. Gelation during polymerization tends to occur, which is not preferable. The molecular weight of the hydrophobic copolymerizable polyester resin is preferably in the range of 5000 to 50000 on a weight average. If the molecular weight is less than 5,000, the adhesiveness of the printed layer may be lowered. Conversely, if it exceeds 50,000, problems such as gelation during polymerization may occur.

(Graft site of polyester graft copolymer)
The polymerizable unsaturated monomer to be grafted to the hydrophobic copolymerizable polyester resin is a hydrophilic radical polymerizable monomer, and is a radical polymerization having a hydrophilic group or a group that can be changed to a hydrophilic group later. It is a possible monomer. Examples of the hydrophilic group include a carboxyl group, a hydroxyl group, a phosphoric acid group, a phosphorous acid group, a sulfonic acid group, an amide group, and a quaternary ammonium base. On the other hand, examples of the group that can be changed to a hydrophilic group include an acid anhydride group, a glycidyl group, and a chloro group. Among these groups, a carboxyl group is preferable from the viewpoint of increasing the water dispersibility and the acid value of the graft copolymer. Accordingly, it is desirable to include at least one acid anhydride having a double bond as the polymerizable unsaturated monomer.

  Examples of the polymerizable unsaturated monomer include fumaric acid, monoethyl fumarate, diethyl fumarate, diester of fumaric acid such as dibutyl fumarate; maleic acid and its anhydride, monoethyl maleate, diethyl maleate Monoester or diester of maleic acid such as dibutyl maleate; itaconic acid and its anhydride, monoester or diester of itaconic acid; maleimide such as phenylmaleimide; styrene, α-methylstyrene, t-butylstyrene, chloromethyl Styrene derivatives such as styrene; vinyltoluene, divinylbenzene and the like. Acrylic polymerizable monomers that are one of polymerizable unsaturated monomers include, for example, alkyl acrylate, alkyl methacrylate (the alkyl group is methyl, ethyl, n-propyl, isopropyl, n-butyl). Group, isobutyl group, t-butyl group, 2-ethylhexyl group, cyclohexyl group, phenyl group, benzyl group, phenylethyl group, etc.): 2-hydroxyethyl acrylate, 2-hydroxyethyl methacrylate, 2-hydroxypropyl acrylate, 2- Hydroxypropyl methacrylate-containing acrylic monomer: acrylamide, methacrylamide, N-methyl methacrylamide, N-methyl acrylamide, N-methylol acrylamide, N-methylol methacrylamide, N, N-dimethylol acrylamide N-methoxymethylacrylamide, N-methoxymethylmethacrylamide, amide group-containing acrylic monomer of N-phenylacrylamide: N, N-diethylaminoethyl acrylate, amino group-containing acrylic monomer of N, N-diethylaminoethyl methacrylate : Glycidyl acrylate, epoxy group-containing acrylic monomer of glycidyl methacrylate: Acrylic monomers containing carboxyl groups or salts thereof such as acrylic acid, methacrylic acid and their salts (sodium salt, potassium salt, ammonium salt) It is done. However, acrylic polymerizable monomers are less preferred for use in the present invention because they are less effective in reducing the surface energy hydrogen bond strength component term (γsh) of the present invention. The polymerizable unsaturated monomer can be copolymerized using one kind or two or more kinds, but preferably contains at least one acid anhydride having a double bond. Among the above monomers, maleic anhydride is preferably used as the acid anhydride having a double bond. Styrene is preferred as another polymerizable unsaturated monomer to be combined with maleic anhydride. These acid anhydride esters may also be included.

(Polymerization initiator and other additives)
As the graft polymerization initiator that can be used in the present invention, organic peroxides and organic azo compounds known to those skilled in the art can be used. Benzoyl peroxide, t-butylperoxypivalate as organic peroxide, 2,2′-azobisisobutyronitrile, 2,2′-azobis (2,4-dimethylvaleronitrile) as organic azo compound Etc. The amount of the polymerization initiator used for the graft polymerization is at least 0.2% by mass, preferably 0.5% by mass or more, based on the polymerizable unsaturated monomer. In addition to the polymerization initiator, a chain transfer agent for adjusting the chain length of the branched polymer, for example, octyl mercaptan, mercaptoethanol, 3-t-butyl-4-hydroxyanisole and the like may be used as necessary. In this case, it is desirable to add in the range of 0 to 5% by mass with respect to the polymerizable unsaturated monomer.

  The copolymer polyester preferably has water solubility or water dispersibility from the viewpoint of coatability. As such a copolyester, a copolyester having at least one group selected from the group consisting of sulfonic acid groups or alkali metal bases thereof (hereinafter referred to as sulfonic acid group-containing copolyester) is used. Is preferred.

  Here, the sulfonic acid group-containing copolymer polyester means a polyester in which at least one group selected from the group consisting of a sulfonic acid group or an alkali metal base thereof is bonded to a part of a dicarboxylic acid component or a glycol component. However, a co-polymer prepared by using an aromatic dicarboxylic acid component containing at least one group selected from the group consisting of a sulfonic acid group or an alkali metal base thereof in a ratio of 2 to 10 mol% with respect to the total acid component. Polymerized polyester is preferred.

  As an example of such a dicarboxylic acid, 5-sodium sulfoisophthalic acid is suitable. In this case, as other dicarboxylic acid components, terephthalic acid, isophthalic acid, phthalic acid, p-β-oxyethoxybenzoic acid, 2,6-naphthalenedicarboxylic acid, 4,4′-dicarboxydiphenyl, 4,4 ′ -Dicarboxybenzophenone, bis (4-carboxyphenyl) ethane, adipic acid, sebacic acid, cyclohexane-1,4-dicarboxylic acid and the like.

  In order to increase the surface hardness and maintain good blocking resistance, 96 to 90 mol% of the total acid content is preferably an aromatic dicarboxylic acid such as terephthalic acid or isophthalic acid. More preferably, 4 to 10 mol% of the aromatic dicarboxylic acid contains at least one group selected from the group consisting of the sulfonic acid groups or alkali metal bases thereof.

  As the glycol component for producing the sulfonic acid group-containing copolymer polyester, ethylene glycol is mainly used. In addition, addition of propylene glycol, butanediol, neopentyl glycol, diethylene glycol, cyclohexanedimethanol, bisphenol A ethylene oxide addition Products, polyethylene glycol, polypropylene glycol, polytetramethylene glycol, and the like can be used. Among them, it is preferable to use ethylene glycol, propylene glycol, butanediol, neopentyl glycol, diethylene glycol, cyclohexane dimethanol or the like as a copolymerization component in terms of improving compatibility with polystyrene sulfonate.

  In addition, a dicarboxylic acid component or glycol component containing a small amount of an amide bond, a urethane bond, an ether bond, a carbonate bond, or the like may be included as a copolymer component of the copolymer polyester. Furthermore, in order to improve the surface hardness of the resulting coating film, a monomer containing a multi-carboxyl group such as trimellitic acid, trimesic acid, pyromellitic acid, trimellitic anhydride, pyromellitic anhydride is contained in a proportion of 5 mol% or less. It can also be used as a copolymerization component of the polyester. When these multi-carboxyl group-containing monomers exceed 5 mol%, the resulting sulfonic acid group-containing copolymer polyester becomes thermally unstable and is unfavorably easily gelled.

  The sulfonic acid group-containing copolymer polyester is obtained, for example, by esterification, transesterification, polycondensation reaction, etc. by a conventional method using the dicarboxylic acid component, the glycol component, and, if necessary, a multi-carboxyl group-containing monomer. be able to. The obtained sulfonic acid group-containing copolymer polyester is heated and stirred together with a solvent such as n-butyl cellosolve, and can be used as an aqueous solution or aqueous dispersion by gradually adding water while stirring.

(Polycarbonate polyurethane)
In the present invention, polyurethane imparts the flexibility of the easily adhesive layer and is added for excellent moldability. However, when the flexibility due to polyurethane is increased, blocking resistance and heat-and-moisture resistance in high-speed processing under heating conditions may further decrease. Therefore, in the present invention, polycarbonate polyurethane is used as the polyurethane.

  Polyurethanes are broadly classified into polyester polyurethanes, polyether polyurethanes, and polycarbonate polyurethanes. Polyester polyurethanes are easy to hydrolyze in wet heat environments, and polyether polyurethanes are highly hygroscopic, so the film strength of the easily adhesive layer It is easy to fall and adhesiveness is insufficient. On the other hand, polycarbonate-based polyurethane has a polycarbonate structure as a hard segment, and therefore has excellent moisture and heat resistance. This is the reason why the polycarbonate-based polyurethane is used in the present invention.

  As the polycarbonate-based polyurethane resin, a polycarbonate diol, an aliphatic and / or alicyclic diisocyanate, and a polymer to which a chain extender is added as necessary can be used. Note that these urethane constituents can be identified by nuclear magnetic resonance analysis or the like.

  The polycarbonate diol is represented by the following general formula.

HO — [— R—O—COO—] _n —R—OH
(R is an aliphatic or alicyclic substituent)

  The polycarbonate diol is obtained, for example, by reacting one or more compounds selected from the group consisting of alkylene carbonate, diaryl carbonate, and dialkyl carbonate with diols and / or polyether polyols.

  Examples of the alkylene carbonate include ethylene carbonate, 1,2-propylene carbonate, 1,2-butylene carbonate and the like.

  Examples of diaryl carbonates include diphenyl carbonate, phenyl-naphthyl carbonate, dinaphthyl carbonate, 4-methyl diphenyl carbonate, 4-ethyl diphenyl carbonate, 4-propyl diphenyl carbonate, 4,4'-dimethyl-diphenyl carbonate, 4,4 Examples include '-diethyl-diphenyl carbonate and 4,4'-dipropyl-diphenyl carbonate.

  Examples of dialkyl carbonates include dimethyl carbonate, diethyl carbonate, di-n-propyl carbonate, diisopropyl carbonate, di-n-butyl carbonate, diisobutyl carbonate, di-t-butyl carbonate, di-n-amyl carbonate, diisoamyl carbonate. Etc.

  As a co-reactant for these carbonates, as examples of diols, ethylene glycol, 1,2-propanediol, 1,3-propanediol, 1,3-butanediol, 1,4-butanediol, 2- Methyl-1,3-propanediol, neopentyl glycol, 2-methyl-pentanediol, 3-methyl-pentanediol, 2,2,4-trimethyl-1,6-hexanediol, 2,3,5-trimethylpentane Diol etc. are mentioned.

  Examples of polyether polyols include polytetramethylene glycol obtained by ring-opening polymerization of tetrahydrofuran and alkylene oxide adducts of diols. Examples of diols used herein include, for example, ethylene glycol, 1,2-propanediol, 1,3-propanediol, 1,3-butanediol, 1,4-butanediol, isomer pentanediols, and isomer hexane. Diols or octanediols such as 2-ethyl-1,3-hexanediol, 1,2-bis (hydroxymethyl) -cyclohexanone, 1,3-bis (hydroxymethyl) -cyclohexanone, 1,4-bis (hydroxymethyl) ) -Cyclohexanone, trimethylolpropane, glycerin and the like. Examples of alkylene oxides include ethylene oxide, propylene oxide, 1,2-butylene oxide, 1,3-butylene oxide, 2,3-butylene oxide, and tetrahydrofuran. , Styrene oxide, epichlorohydrin and the like, which are also possible to use a mixture of two or more.

  The diols and polyether polyols described above may be used alone or in combination of two or more. Any of these can react with one or more compounds selected from the group consisting of the aforementioned alkylene carbonates, diaryl carbonates, and dialkyl carbonates by known methods to form polycarbonate diols.

  In the present invention, the composition molar ratio of the polycarbonate polyol, which is a constituent component of urethane, is preferably 3 to 100 mol%, and preferably 5 to 50 mol% when the total polyisocyanate component of urethane is 100 mol%. It is more preferable that the content is 6 to 20 mol%. When the composition molar ratio is low, the heat and moisture resistance effect of the polycarbonate polyol may not be obtained. Moreover, when the said composition molar ratio is high, adhesiveness may fall.

  Examples of the polyisocyanate that is a constituent component of the urethane of the present invention include isomers of toluylene diisocyanate, aromatic diisocyanates such as 4,4-diphenylmethane diisocyanate, aromatic aliphatic diisocyanates such as xylylene diisocyanate, and isophorone. Diisocyanates and alicyclic diisocyanates such as 4,4-dicyclohexylmethane diisocyanate, 1,3-bis (isocyanatomethyl) cyclohexane, hexamethylene diisocyanate, and aliphatic diisocyanates such as 2,2,4-trimethylhexamethylene diisocyanate, Alternatively, polyisocyanates obtained by adding one or more of these compounds with trimethylolpropane or the like in advance may be mentioned.

  Chain extenders include glycols such as ethylene glycol, diethylene glycol, 1,4-butanediol, neopentyl glycol and 1,6-hexanediol, polyhydric alcohols such as glycerin, trimethylolpropane, and pentaerythritol, ethylenediamine Diamines such as hexamethylenediamine and piperazine, aminoalcohols such as monoethanolamine and diethanolamine, thiodiglycols such as thiodiethylene glycol, and water.

  The easy-adhesion layer of the present invention is preferably provided by an in-line coating method described later using an aqueous coating solution. Therefore, it is desirable that the urethane resin of the present invention is water-soluble. The “water-soluble” means that it dissolves in water or an aqueous solution containing less than 50% by mass of a water-soluble organic solvent.

  In order to impart water solubility to the urethane resin, a sulfonic acid (salt) group or a carboxylic acid (salt) group can be introduced (copolymerized) into the urethane molecular skeleton. Since the sulfonic acid (salt) group is strongly acidic and it may be difficult to maintain moisture resistance due to its hygroscopic performance, it is preferable to introduce a weakly acidic carboxylic acid (salt) group.

  In order to introduce a carboxylic acid (salt) group into a urethane resin, for example, as a polyol component, a polyol compound having a carboxylic acid group such as dimethylolpropionic acid or dimethylolbutanoic acid is introduced as a copolymer component to form a salt. Neutralize with an agent. Specific examples of the salt forming agent include trialkylamines such as ammonia, trimethylamine, triethylamine, triisopropylamine, tri-n-propylamine, tri-n-butylamine, N such as N-methylmorpholine and N-ethylmorpholine. -N-dialkylalkanolamines such as alkylmorpholines, N-dimethylethanolamine, N-diethylethanolamine and the like. These can be used alone or in combination of two or more.

  In order to impart water solubility, when a polyol compound having a carboxylic acid (salt) group is used as a copolymerization component, the composition molar ratio of the polyol compound having a carboxylic acid (salt) group in the urethane resin is the same as that of the urethane resin. When the total polyisocyanate component is 100 mol%, it is preferably 3 to 60 mol%, more preferably 10 to 40 mol%. If the composition molar ratio is less than 3 mol%, water dispersibility may be difficult.

  In the present invention, the glass transition point (Tig) of the polycarbonate-based polyurethane is preferably controlled within a specific range. That is, the glass transition point (Tig) of the polyurethane of the present invention has a lower limit of 40 ° C., preferably 50 ° C., and an upper limit of 100 ° C., preferably 90 ° C. When the glass transition point (Tig) of the polyurethane resin is less than 40 ° C., the blocking resistance may be lowered. On the other hand, when the temperature exceeds 100 ° C., the flexibility and adhesiveness of the easy-adhesion layer may decrease. In order to control the glass transition point (Tig) of the polyurethane within the above range, the following polyol component or molecular weight of the polyurethane can be appropriately selected and adjusted.

  In the present invention, the blending ratio of the copolymer polyester and the polyurethane is such that the polyester / polyurethane (mass ratio) = 80 / 20-30 / 70 is preferable. The blending ratio is more preferably 75/25 to 40/60. When the copolyester / polyurethane (mass ratio) = 100/0 to 90/10, the flexibility of the easy-adhesion layer may be lowered, and when 20/80 to 0/100, the blocking resistance and the adhesion may be lowered.

  The easy-adhesion layer of the present invention is mainly composed of a polyester that exhibits suitable adhesion to a base film made of polyester and polyurethane that is highly compatible with printing inks, and therefore has excellent initial adhesion. Indicates. Furthermore, a polyester-based graft copolymer capable of forming a high degree of self-crosslinking property is used as the polyester, and a polycarbonate-based polyurethane that is hardly hydrolyzed is used as the polyurethane. Therefore, it is possible to maintain not only initial adhesion but also excellent adhesion (moisture heat resistance) even in a wet heat environment. The present inventor considers that the combination of the polyester-based graft copolymer and the polycarbonate-based polyurethane is particularly suitable for imparting wet heat resistance as follows. That is, the polyester-based graft copolymer of the present invention has an acid anhydride as a constituent component as a side chain. On the other hand, the polyurethane of the present invention has a carbonate group. These side chains and carbonate groups exhibit a hydrogen bond-like interaction, and it is considered that the durability as an easy adhesion layer is exhibited to a higher degree. In any case, in the present invention, by using a polyester-based graft copolymer and a polycarbonate-based polyurethane as the easy-adhesion layer, the characteristics excellent in adhesion and heat-and-moisture resistance are exhibited.

(Crosslinking agent)
From the viewpoint of blocking resistance, the easy-adhesion layer of the present invention preferably contains a crosslinking agent. Thereby, an appropriate cross-linked structure is formed in the easy-adhesion layer, and therefore the addition of a cross-linking agent is suitable for imparting moisture heat resistance. The blending ratio of the crosslinking agent is preferably 5 to 40 parts by mass, more preferably 8 to 25 parts by mass with respect to 100 parts by mass of the total amount of the copolyester and polyurethane. If the blending ratio of the crosslinking agent is less than 5 parts by mass with respect to 100 parts by mass of the total amount of the copolymerized polyester and polyurethane, the blocking resistance may be lowered or the adhesiveness may be lowered. Conversely, when it exceeds 40 parts by mass, the flexibility for following the moldability may be reduced.

  Examples of the cross-linking agent include phenol formaldehyde resins of condensates with formaldehyde such as alkylated phenols and cresols; adducts of urea, melamine, benzoguanamine, and the like with formaldehyde, and the adducts having 1 to 6 carbon atoms. An amino resin such as an alkyl ether compound composed of alcohol; a polyfunctional epoxy compound; a polyfunctional isocyanate compound; a blocked isocyanate compound; a polyfunctional aziridine compound;

  Examples of the phenol formaldehyde resin include alkylated (methyl, ethyl, propyl, isopropyl or butyl) phenol, p-tert-amylphenol, 4,4′-sec-butylidenephenol, p-tert-butylphenol, o-, m-, p-cresol, p-cyclohexylphenol, 4,4'-isopropylidenephenol, p-nonylphenol, p-octylphenol, 3-pentadecylphenol, phenol, phenyl-o-cresol, p-phenylphenol, xylenol, etc. And the condensates of phenols and formaldehyde.

  Examples of amino resins include methoxylated methylol urea, methoxylated methylol N, N-ethyleneurea, methoxylated methylol dicyandiamide, methoxylated methylol melamine, methoxylated methylol benzoguanamine, butoxylated methylol melamine, butoxylated methylol benzoguanamine, and the like. Are preferably methoxylated methylol melamine, butoxylated methylol melamine, methylolated benzoguanamine, and the like.

  Examples of the polyfunctional epoxy compound include diglycidyl ether of bisphenol A and oligomer thereof, diglycidyl ether of hydrogenated bisphenol A and oligomer thereof, orthophthalic acid diglycidyl ester, isophthalic acid diglycidyl ester, terephthalic acid diglycidyl ester, p-oxybenzoic acid diglycidyl ester, tetrahydrophthalic acid diglycidyl ester, hexahydrophthalic acid diglycidyl ester, succinic acid diglycidyl ester, adipic acid diglycidyl ester, sebacic acid diglycidyl ester, ethylene glycol diglycidyl ether, propylene Glycol diglycidyl ether, 1,4-butanediol diglycidyl ether, 1,6-hexanediol diglycidyl ether and Polyalkylene glycol diglycidyl ethers, trimellitic acid triglycidyl ester, triglycidyl isocyanurate, 1,4-diglycidyloxybenzene, diglycidyl propylene urea, glycerol triglycidyl ether, trimethylolpropane triglycidyl ether, pentaerythritol triglycidyl Examples include ether, triglycidyl ether of glycerol alkylene oxide adduct, and the like.

  As the polyfunctional isocyanate compound, a low-molecular or high-molecular aromatic or aliphatic diisocyanate or a trivalent or higher polyisocyanate can be used. Polyisocyanates include tetramethylene diisocyanate, hexamethylene diisocyanate, toluene diisocyanate, diphenylmethane diisocyanate, hydrogenated diphenylmethane diisocyanate, xylylene diisocyanate, hydrogenated xylylene diisocyanate, isophorone diisocyanate, and trimers of these isocyanate compounds. Furthermore, an excess amount of these isocyanate compounds and low molecular active hydrogen compounds such as ethylene glycol, propylene glycol, trimethylolpropane, glycerin, sorbitol, ethylenediamine, monoethanolamine, diethanolamine, triethanolamine, or polyester polyols, poly The terminal isocyanate group containing compound obtained by making it react with polymer active hydrogen compounds, such as ether polyols and polyamides, can be mentioned.

  Among the crosslinking agents, a blocked isocyanate crosslinking agent is preferable as the crosslinking agent used in the present invention. By adding a blocked isocyanate-based crosslinking agent, it becomes possible to achieve both high adhesiveness and blocking resistance.

  The blocked isocyanate crosslinking agent can be prepared by subjecting the isocyanate compound and the blocking agent to an addition reaction by a conventionally known appropriate method. Examples of the isocyanate blocking agent include phenols such as phenol, cresol, xylenol, resorcinol, nitrophenol, and chlorophenol; thiophenols such as thiophenol and methylthiophenol; oximes such as acetoxime, methyl etiketooxime, and cyclohexanone oxime. Alcohols such as methanol, ethanol, propanol and butanol; halogen-substituted alcohols such as ethylene chlorohydrin and 1,3-dichloro-2-propanol; tertiary alcohols such as t-butanol and t-pentanol ; Lactams such as ε-caprolactam, δ-valerolactam, γ-butyrolactam, β-propyllactam; aromatic amines; imides; acetylacetone, acetoacetate Active methylene compounds such as malonic acid ethyl ester; mercaptans; imines; ureas; diaryl compounds; and sodium bisulfite and the like.

  It is preferable that isocyanate group content in a block isocyanate type crosslinking agent is 3.0-15.0 mass%. The isocyanate group content in the blocked isocyanate crosslinking agent is more preferably 4.0 to 10.0% by mass, further preferably 4.5 to 9.0% by mass, and 5.0 to 8. More preferably, it is 0 mass%. If the isocyanate group content in the blocked isocyanate crosslinking agent is less than 3.0% by mass, the ink adhesion deteriorates, which is not preferable. On the other hand, if it exceeds 15.0% by mass, the adhesiveness deteriorates, which is not preferable.

  In addition, when using the said block isocyanate type crosslinking agent, it evaluates as a reproduction | regeneration isocyanate group (reproduction | regeneration NCO) content which reproduces | regenerates and evaluates by the below-mentioned method.

(particle)
In this invention, in order to improve the blocking resistance of an easily bonding layer, it is also a preferable aspect to add particle | grains to an easily bonding layer. Examples of the particles contained in the easy-adhesion layer in the present invention include titanium oxide, barium sulfate, calcium carbonate, calcium sulfate, silica, alumina, talc, kaolin, clay and the like, or a mixture thereof. Inorganic particles such as calcium phosphate, mica, hectorite, zirconia, tungsten oxide, lithium fluoride, calcium fluoride and other inorganic particles, styrene-based, acrylic-based, melamine-based, benzoguanamine-based, silicone-based Examples include organic polymer particles.

  The average particle size of the sex particles in the easy-adhesion layer (number-based average particle size by SEM; the same applies hereinafter) is preferably 0.04 to 2.0 μm, more preferably 0.1 to 1.0 μm. If the average particle size of the inert particles is less than 0.04 μm, the formation of irregularities on the film surface becomes insufficient, so that the handling properties such as the slipping property and the winding property of the film are lowered, and the molding is performed. May also decrease. On the other hand, if it exceeds 2.0 μm, the particles are likely to fall off, which is not preferable. The particle concentration in the easy-adhesion layer is preferably 0.01 to 1.0% by mass and more preferably 0.05 to 0.5% by mass in the solid component.

  In the present invention, the thickness of the easy-adhesion layer can be appropriately set in the range of 0.001 to 2.00 μm, but in the range of 0.01 to 1.00 μm to achieve both workability and adhesiveness. More preferably, it is 0.02-0.80 micrometer, More preferably, it is 0.05-0.50 micrometer. Adhesiveness will become inadequate that the thickness of an easily bonding layer is less than 0.01 micrometer. When the thickness of the easy-adhesion layer exceeds 2.00 μm, blocking may occur.

  In the coating liquid of the present invention, known additives, for example, antioxidants, heat stabilizers, weathering stabilizers, UV absorbers, organic lubricants, pigments, dyes, organics, as long as the effects of the present invention are not impaired. Alternatively, inorganic particles, an antistatic agent, a nucleating agent, or the like may be added.

(Antistatic agent)
When the film of the present invention is used as a member of an information recording body such as an IC card, a preferred embodiment has a surface specific resistance value of 1 × 10 ⁶ to 10 ¹³ Ω / □ on the surface of the easily adhesive layer at 25 ° C. and 65% RH. Preferably there is. By setting the surface resistance value within the above range, dampening water suitability (water loss) at the time of printing is deteriorated, and troubles such as blurring and bleeding are likely to occur.

  In order to make the surface specific resistance value on the surface of the easy-adhesion layer within the above range, it is preferable to add an antistatic agent to the easy-adhesion layer. The type of the antistatic agent to be used is not limited as long as it does not inhibit the effect of the present invention. However, it is preferable to use a polymer antistatic agent having at least one sulfonate group or phosphate group in the molecule. This polymer antistatic agent is characterized by a structure having a large number of highly hydrophilic sulfonic acid components and phosphoric acid components. These polymer antistatic agents may be used alone or in combination of two or more.

  Resins containing a sulfonate group component in the molecule include polystyrene sulfonic acid sodium salts, potassium salts, lithium salts, ammonium salts, homopolymers such as phosphonium salts, and acrylic monomers such as acrylic acid esters or methacrylic acid esters. And a copolymer of styrene sulfonic acid monomer and a copolymer of acrylamidomethylpropane sulfonic acid and unsaturated monomer. In the present invention, the sulfonate can be a mixture of a metal salt and an amine salt.

  Examples of the resin containing a phosphate group in the molecule include resins obtained by polymerizing or copolymerizing various phosmers (manufactured by Unichemical) which are unsaturated monomers containing a phosphate group.

  The weight average molecular weight of the antistatic agent is preferably in the range of 1,000 to 1,000,000, more preferably 5,000 to 1,000,000. When the weight average molecular weight is less than 1,000, the coating film is excellent in gloss, but the water-resistant adhesion of the coating film is hardly obtained. On the other hand, if it exceeds 1,000,000, the water-resistant adhesion becomes high, but uniform mixing with the modified resin becomes difficult, and the gloss of the coating film tends to decrease.

  In order to make the surface resistivity value on the surface of the easy-adhesion layer within the above range, the content of the sulfonate group-containing antistatic agent is preferably 5% by mass or more based on the resin composition of the easy-adhesion layer. However, when the content exceeds 60% by mass, the adhesion strength to the base film, film strength, and solvent resistance may be insufficient.

(Base film)
The polyester used for the base material of the present invention is an aromatic dicarboxylic acid or ester thereof such as terephthalic acid, isophthalic acid or naphthalenedicarboxylic acid and glycol such as ethylene glycol, diethylene glycol, 1,4-butanediol or neopentyl glycol. Polyester produced by polycondensation. These polyesters include (1) a method in which an aromatic dicarboxylic acid and glycol are directly reacted and then a polycondensation reaction (direct weight method), and (2) an alkyl ester of an aromatic dicarboxylic acid and glycol. It can be produced by a known method such as a method of performing an exchange reaction and then a polycondensation reaction (transesterification method), or a method of (3) polycondensation of diglycol esters of aromatic dicarboxylic acids.

  Representative examples of such polyesters include polyethylene terephthalate, polybutylene terephthalate, polypropylene terephthalate, or polyethylene-2,6-naphthalate. These polyesters may be homopolymers or copolymerized with a third component. In any case, in the present invention, the ethylene terephthalate unit, butylene terephthalate unit, propylene terephthalate unit, or ethylene-2,6-naphthalate unit is 70 mol% or more, preferably 80 mol% or more, more preferably 90 mol% or more. The polyester which is is preferable. Among these, polyethylene terephthalate is particularly preferable from the viewpoint of cost performance. The intrinsic viscosity of the base film is preferably 0.50 to 0.70 dl / g.

  From the viewpoint of imparting whiteness and hiding properties to the polyester film of the base material and improving the print sharpness, the base material contains a white pigment and / or inorganic particles.

  As the white pigment used in the present invention, titanium oxide, barium sulfate, zinc oxide, zinc sulfide, calcium carbonate and the like can be used. The white pigment can be subjected to various organic and inorganic surface treatments for the purpose of improving dispersibility. In particular, among white pigments, titanium oxide is preferable because it has a high refractive index and can exhibit high whiteness and concealment with a small amount. Further, it is preferable to use a fluorescent brightening agent in combination because the whiteness can be further improved.

  The lower limit of the content of the white pigment in the base film is preferably 10% by mass, particularly preferably 15% by mass, from the viewpoint of concealability. The upper limit of the content of the white pigment is preferably 45% by mass, more preferably 35% by mass, and particularly preferably 25% by mass from the viewpoint of film formation stability.

  In addition, in order to further increase the whiteness, when a fluorescent whitening agent is used in addition to the white pigment in the base film, if the white pigment exceeds 45% by mass, the amount of ultraviolet absorption of the white pigment increases, and thus the fluorescence enhancement. Ultraviolet rays necessary for the whitening agent to exert its effect are reduced, the fluorescent whitening effect is remarkably inhibited, and the whiteness is lowered.

  Further, in order to further improve the concealability of the film, a small amount of a color pigment such as carbon black may be contained in addition to the white pigment. Further, in order to provide other functions, the layer A requires inorganic particles having a smaller average particle diameter than the white pigment, heat-resistant organic particles, antioxidants, crosslinking agents, ultraviolet absorbers, plasticizers, and the like. It can be contained accordingly.

  It is also desirable that the base film contains a white pigment and at least one inorganic particle having an average particle size larger than that of the white pigment. As the inorganic particles, white pigments such as titanium oxide, barium sulfate, zinc oxide, zinc sulfide, and calcium carbonate may be used, or inorganic particles having a small difference in refractive index from polyester such as silica may be used. When two types of white pigments having different average particle diameters are used, the white pigments may be the same type or different types. In short, it is desirable from the viewpoint of concealment and handling properties that two types of inorganic particles having different average particle sizes are used and the inorganic particles having a small average particle size are white pigments. As the inorganic particles having a large average particle size, silica is preferable from the viewpoints of cost and handleability.

  The upper limit of the average particle diameter of the inorganic particles contained in the base film is important to be 5.0 μm, preferably 3.0 μm, from the viewpoint of printing quality when providing a printed layer or the like by post-processing. Particularly preferably, it is 2.0 μm. Further, the lower limit of the average particle diameter of the inorganic particles contained in the base film is preferably 0.5 μm, particularly preferably from the viewpoint of slipperiness in the film production process and the post-processing process. 7 μm.

  Moreover, it is preferable to make content of the inorganic particle in a base film smaller than content of a white pigment with a small average particle diameter from the point of print quality and slipperiness. Further, from the viewpoint of improving the printing quality, the upper limit of the content of inorganic particles in the base film is preferably 4000 ppm, particularly preferably 2000 ppm. Moreover, it is preferable that content of the inorganic particle in a base film has a lower limit of 50 ppm from the point which improves slipperiness further, Most preferably, it is 100 ppm.

  The base film of the present invention may be a single layer or a multilayer. For example, when the layer containing the white pigment and / or inorganic particles is an A layer and the other layers are a B layer and a C layer, A / B / A, A / B / C, C / A / B / Layer configurations such as A, C / A / B / A / C, C / A / B, etc. can be selected. In particular, when the B / A / B layer has a two-type / three-layer configuration, the B layer may not contain particles, and in order to further improve the concealing property, a white pigment, Inorganic particles and heat-resistant organic particles may be included. Furthermore, in order to further improve the whiteness, a fluorescent whitening agent may be contained in the B layer as long as the effects of the present invention are not impaired.

  When the B / A / B layer has a two-layer / three-layer configuration, the A layer of the base material contains white pigments and inorganic particles. The upper limit is preferably 50% with respect to the total thickness of the laminated film. Further, the lower limit of the total thickness of the A layer is preferably 10% from the viewpoint of whiteness and concealment.

  In addition, the base material film used in the present invention contains a polyester resin and a thermoplastic resin incompatible with the polyester resin as a cavity forming agent, and then formed a cavity by stretching in at least one direction. It may be a film.

  Examples of thermoplastic resins that are incompatible with polyester resins include polyolefin resins, polystyrene resins, polyacrylic resins, polycarbonate resins, polysulfone resins, cellulose resins, polyphenylene ether resins, and the like. It is not limited. Among the incompatible thermoplastic resins, it is preferable that a polyolefin resin and a polystyrene resin are included as essential components.

When using the said void containing film as a base film, it is preferable that the apparent density of a film shall be 0.5 g / cm < ³ > or more from the point of film strength. In particular, when used as an information recording material or a printing material such as a magnetic card or an IC card, the lower limit of the apparent density is preferably 0.8 g / cm ³ , more preferably from the viewpoint of the back feeling (rigidity) of the film. Is preferably 0.9 g / cm ³ , particularly preferably 1.0 g / cm ³ . The base material of the white laminated polyester film of the present invention preferably has an apparent density of 1.3 g / cm ³ or more. When it is less than 1.3 g / cm ^3, the stiffness of the film becomes weak, and the rigidity is insufficient when used as an information recording material or printing material. The apparent density of the base film can be controlled by the type (density) of polyester after crystal orientation, the type (density) of white pigments and inorganic particles, the content, and the like.

  Moreover, although the total thickness of a laminated | multilayer film should just adjust suitably according to a use, generally it is 25-250 micrometers. Moreover, when using for card | curd base materials, such as an IC card and a magnetic card, it is 100-250 micrometers normally.

(Production method)
The white laminated polyester film of the present invention is preferably a biaxially oriented laminated polyester obtained by sequential biaxial stretching or simultaneous biaxial stretching. Hereinafter, the most preferred sequential biaxial stretching method will be described.

  After sufficiently vacuum-drying the film raw material, it is melted by an extruder and extruded from a T-die into a sheet to obtain an unstretched film.

  At this time, the white pigment and other additives are not added to the extruder and kneaded, but a masterbatch polymer in which the white pigment and the like are separately contained in the polyester resin at a high concentration is prepared in advance. Is preferable from the viewpoint of uniform mixing. As the extruder, it is preferable to use a twin-screw extruder in order to mix various film raw materials more sufficiently and uniformly.

  In the present invention, the polyester film of the base material may have a single layer structure or a multilayer structure. However, in the case of a laminated structure, after the resins of the A layer and the B layer are supplied to separate extruders, for example, molten It is most preferable to adopt a co-extrusion method in which a two-layer structure of A layer / B layer in the state is laminated in a three-layer configuration of A layer / B layer / A layer and extruded from the same die.

  Thereafter, the uniaxially stretched polyester film was guided to a grip-type lateral stretching machine, heated to 80 to 180 ° C., stretched 2.5 to 5.0 times in the lateral direction, and then heat-set at 200 to 240 ° C. Then, if necessary, it is relaxed by 1 to 10% in the longitudinal direction and / or the transverse direction, and then wound up with a film winder to obtain a biaxially stretched polyester film.

As the step of applying the easy-adhesion layer, any method such as a method of applying before stretching of the film, a method of applying after longitudinal stretching, or a method of applying to the film surface after the orientation treatment is possible. The in-line coating method, which is applied before the completion of the crystal orientation of the material polyester film and then stretched in at least one direction and then completes the crystal orientation of the polyester film, can exhibit the effects of the present invention more remarkably. Therefore, it is a preferable method.

  As a method for providing an easy-adhesion layer, a conventionally used method such as a gravure coating method, a kiss coating method, a dip method, a spray coating method, a curtain coating method, an air knife coating method, a blade coating method, or a reverse roll coating method can be applied.

  Next, examples and comparative examples of the present invention will be shown. First, the measurement / evaluation method used in the present invention is shown below.

(1) Glass transition point (Tig)
The glass transition point (Tig) of the easy-adhesion layer was measured by scraping only the easy-adhesion layer from the easy-adhesion film.
The measurement was based on JIS K7121 and the glass transition start temperature (Tig) was calculated | required from the DSC curve using the differential scanning calorimeter (The Seiko Instruments Inc. make, DSC6200).
Measurement conditions (a) Measurement temperature range: 0 to 200 ° C
(B) Temperature increase rate: 20 ° C./min
(C) With nitrogen gas flow

(2) Intrinsic Viscosity 0.1 g of the chip sample was precisely weighed and dissolved in 25 ml of a mixed solvent of phenol / tetrachloroethane = 6/4 (mass ratio), and measured at 30 ° C. using an Ostwald viscometer. In addition, the measurement was performed 3 times and the average value was calculated | required.

(3) Thickness of easy-adhesion layer A film cross section is cut at right angles to the film surface with a microtome, a cross-sectional photograph of the film is taken with a transmission electron microscope (TEM), and the thickness of the resin component is measured on the photograph. The same measurement was performed 10 times at different locations, and the average of the measured values was taken as the resin component thickness (μm).

(4) Adhesive UV curable ink (manufactured by Seiko Advance Co., Ltd., UVA710 Black) is printed on the film surface (the surface of the easy-adhesion layer if an easy-adhesion layer is provided) with a Tetron screen (# 300 mesh). Then, UV exposure was performed at 500 mJ / cm ² .
Put a 2mm square 100 square cross-cut surface with a cutter knife on the cured printed layer, and paste cello tape (registered trademark) (manufactured by Nichiban Co., Ltd., CT-24) on it so that no air bubbles enter it. Rub on it to make sure it adheres well. Thereafter, both ends of the ink surface before and after the adhesive tape (registered trademark) were not adhered to each other were pressed by hand and rapidly peeled in the 90 ° direction.
The ink surface after peeling was observed, and the adhesiveness was evaluated on the basis of the following four steps based on the ink residual ratio (treated as the number of pieces peeled even at a part of the square) in 100 squares. ○ was accepted. The easy adhesion referred to in the present invention is defined as having an ink residual ratio of 90% or more when the above evaluation is performed.
A: Residual rate 100% (no peeling at all)
○: Residual rate 90% or more and less than 100% (can be used practically without problems)
Δ: Residual rate of 70% or more and less than 90% (adhesion is slightly weak, and there is a possibility that problems may occur in practice)
X: Residual rate less than 70% (adhesion failure)

(5) Adhesiveness after wet heat Oxidized polymerization ink (manufactured by Jujo Kako Co., Ltd., black) and diluent solvent (manufactured by Jujo Kako Co., Ltd., Tetron) are diluted with ink: diluting solvent = 4: 1, and the film surface (easily When an adhesive layer was provided, the surface was printed on a surface of the easy adhesive layer) using a Tetron screen (# 250 mesh) and then dried in a gear oven at 65 ° C. for 15 minutes.
Next, the ink-printed film is placed in 80 ° C. hot water for 2 minutes. After taking out and wiping away moisture, it is air-dried for 3 hours or more. Subsequently, a crosscut surface of 100 mm square of 2 mm is put on the printing surface with a cutter knife, and cello tape (registered trademark) (manufactured by Nichiban Co., Ltd., CT-24) is pasted on the printed surface so that no air bubbles enter. Rub the top to make sure it is in close contact. Thereafter, both ends of the ink surface before and after the cellophane tape (registered trademark) were not adhered were pressed by hand, and the cross-cut surface was rapidly peeled in the 90 ° direction.
The ink surface after peeling was observed, and the adhesiveness was evaluated on the basis of the following four steps based on the ink residual ratio (treated as the number of pieces peeled even at a part of the square) in 100 squares. ○ was accepted. The easy adhesion referred to in the present invention is defined as having an ink residual ratio of 90% or more when the above evaluation is performed.
A: Residual rate 100% (no peeling at all)
○: Residual rate 90% or more and less than 100% (can be used practically without problems)
Δ: Residual rate of 70% or more and less than 90% (adhesion is slightly weak, and there is a possibility that problems may occur in practice)
X: Residual rate less than 70% (There is a problem with adhesiveness)

(6) Formability (elongation measurement)
Coating liquids A to W having a solid content of 11% by mass are applied to an unstretched polyester film with a Meyer bar # 10 and dried in a gear oven at 100 ° C. for 2 minutes. Further, heat is applied for 30 seconds in a gear oven at 200 ° C. to produce a coated film sample. Subsequently, the film is cut into strips having a length of 25 mm and a width of 80 mm, and squares having a length and width of 10 mm are written. A strip-shaped film sample is placed on a tensile tester, and the film sample piece is pulled at a speed of 90 mm / second by grasping both ends of the film while visually observing the appearance under an environment where the actual temperature of the film sample piece is 110 ° C. The length of the square when the occurrence of the problem was measured.
When the length of the film sample piece after the test was a, the elongation was calculated according to the following formula. (The length of the square of the film before the test is 10 mm)
Elongation (%) = (a−10) × 100/10
Here, those having an elongation of 300% or more are considered excellent in moldability, those having 200% or more and less than 300% are considered to have no problem in moldability, and those having an elongation of 100% or more and less than 200% have problems in moldability. It was judged that there was a problem in moldability if it was less than 100%.
○: Elongation is 100% or more (good moldability)
X: Elongation is less than 100% (formability is poor)

(7) NCO content (regenerated NCO content)
5-100 mg of a sample (adhesive layer component) whose NCO content (regenerated NCO content) is to be measured is precisely weighed into an Erlenmeyer flask having a “sliding” opening. To the above Erlenmeyer flask, 25 ml of a 0.5 mol / l dibutylamine-monochlorobenzene solution is added, and ortho-dichlorobenzene and zeolite are added. Then, a “sliding” bulb condenser that fits the opening of the flask is attached. The above Erlenmeyer flask is placed on a previously prepared heating plate and reacted for 30 minutes after the solvent in the flask starts to boil. Then, after removing the Erlenmeyer flask from the heating plate and cooling to room temperature, 20 to 30 ml of methanol is poured from above the sliding ball tube cooler, and the inner wall of the cooler is washed away with the methanol. After removing the condenser from the Erlenmeyer flask, 100 ml of methanol and one drop of bromophenol blue indicator were put into the Erlenmeyer flask, and 0.5 mol / l hydrochloric acid standard solution was used for the contents of the flask. Perform back titration. At this time, the titer of the hydrochloric acid standard solution required for the titration of the sample is A (ml). A “blank” sample is obtained by performing the same operation as above except that the above heating is not performed. The blank is titrated as above. At this time, the titer of the hydrochloric acid standard solution required for the blank titration is defined as B (ml). The end point of the titration is the point at which the indigo color of the bromophenol blue indicator turns yellow. From the obtained results, the NCO content (regenerated NCO content) is calculated using the following formula.
Effective isocyanate content (mass%) = {(BA) × 42 × 0.5 × f} × 100 / (S × 1000)

(8) Apparent density of film Four films were cut into 5.00 cm squares to prepare samples. Four of these were overlapped, the thickness was changed with a micrometer, and arbitrary 10 locations were measured with four significant figures, and the average value of the stacked thickness was obtained. The average value was divided by 4 and rounded to 3 significant figures to obtain an average thickness per sheet (t: μm). The mass (w: g) of the four samples was measured using an automatic upper pan balance with four significant digits, and the apparent density was determined from the following equation. The apparent density was rounded to 3 significant figures.
Apparent density (g / cm ³ ) = (w × 10 ⁴ ) / (5.00 × 5.00 × t)

(9) Surface resistivity value The film was allowed to stand for 24 hours in an atmosphere of 23 ° C. and 65% RH, and then applied with a surface resistance value measurement device (manufactured by Mitsubishi Yuka Co., Ltd., Hiresta IP). The surface specific resistance value (Ω / □) of the film surface (the surface of the easy adhesion layer when an easy adhesion layer is provided) was measured at 500V.

Example 1
(Preparation of hydrophobic polymerized polyester resin)
In a stainless steel autoclave equipped with a stirrer, thermometer and partial reflux condenser, 218 parts by weight of dimethyl terephthalate, 194 parts by weight of dimethyl isophthalate, 488 parts by weight of ethylene glycol, 200 parts by weight of neopentyl glycol and tetra-N-butyltitanium 0.5 weight part was prepared and transesterification was performed over 4 hours from 160 degreeC to 220 degreeC. Next, 13 parts by weight of fumaric acid and 51 parts by weight of sebacic acid were added, and the temperature was raised from 200 ° C. to 220 ° C. over 1 hour to carry out an esterification reaction. Next, the temperature was raised to 255 ° C. and the reaction system was gradually depressurized, and then reacted for 1 hour 30 minutes under a reduced pressure of 0.22 mmHg to obtain a hydrophobic copolyester resin. The obtained hydrophobic copolyester was light yellow and transparent.

(Preparation of water-dispersed polyester-based graft copolymer)
In a reactor equipped with a stirrer, thermometer, refluxing device and quantitative dropping device, 75 parts by mass of hydrophobic copolymer polyester, 56 parts by mass of methyl ethyl ketone and 19 parts by mass of isopropyl alcohol are heated and stirred at 65 ° C. Dissolved. After the resin was completely dissolved, 15 parts by mass of maleic anhydride was added to the polyester solution. Subsequently, a solution prepared by dissolving 10 parts by mass of styrene and 1.5 parts by mass of azobisdimethylvaleronitrile in 12 parts by mass of methyl ethyl ketone was dropped into the polyester solution at 0.1 ml / min, and stirring was further continued for 2 hours. After sampling for analysis from the reaction solution, 5 parts by mass of methanol was added. Next, 300 parts by mass of ion-exchanged water and 15 parts by mass of triethylamine were added to the reaction solution and stirred for 1.5 hours. Thereafter, the reactor internal temperature was raised to 100 ° C., and methyl ethyl ketone, isopropyl alcohol, and excess triethylamine were distilled off to obtain a water-dispersed polyester graft copolymer. The obtained polyester-based graft copolymer was light yellow and transparent, and the glass transition point was 40 ° C. This resin was designated as a polyester-based graft copolymer (a1).

(Synthesis of polycarbonate urethane resin)
In a four-necked flask equipped with a reflux condenser, a nitrogen inlet tube, a thermometer, and a stirrer, 73.0 parts by mass of 1,3-cyclohexanebis (methyl isocyanate) as polyisocyanate and polyhexane having a number average molecular weight of 2000 Diol carbonate 112.7 parts by mass, neopentyl glycol 11.7 parts by mass, dimethylolpropionic acid 12.6 parts by mass, and as an organic solvent, acetonitrile 60 parts by mass, N-methylpyrrolidone 30 parts by mass, Under a nitrogen atmosphere, the temperature of the reaction solution was adjusted to 75 to 78 ° C., and 0.06 part by mass of stannous octylate was added as a reaction catalyst, and the reaction rate was reacted to 99% or more in 7 hours. Subsequently, this was cooled to 30 degreeC and the isocyanate group terminal prepolymer was obtained. Next, 450 g of water was added to a reaction vessel equipped with a homodisper capable of high-speed stirring, adjusted to 25 ° C., and added with an isocyanate group-terminated prepolymer while stirring and mixing at 2000 min ⁻¹ to disperse in water. did. Thereafter, an aqueous solution (b1) of a water-dispersible polycarbonate-based urethane resin having a solid content of 35% was prepared by removing a portion of acetonitrile and water under reduced pressure. The glass transition point (Tig) was 86 ° C.

(Preparation of coating solution A)
The ratio of the solid content of the polyester-based graft copolymer (a1) and water-dispersible polycarbonate-based urethane resin (b1) obtained above is polyester-based graft copolymer / polyurethane resin (mass ratio) = 95/5. In addition, the block isocyanate compound having an isocyanate group content (regenerated NCO) of 5.4% by mass with respect to 100 parts by mass of the total amount of the polyester-based graft copolymer and the polyurethane resin is mixed so as to be 20 parts by mass. The total resin solid content concentration is 12.0% by mass, and the silica particles having an average particle size of 1.0 μm are 0.44% by mass with respect to the total resin and the silica particles having an average particle size of 0.1 μm are based on the total resin. In order to contain 10% by mass, it was diluted with a mixed solvent of water / isopropyl alcohol (= 65/35; mass ratio) to obtain an aqueous coating agent.

(Film raw material)
Anatase-type titanium dioxide having an average particle diameter of 0.3 μm and a polyethylene terephthalate resin (c) obtained by an ordinary method and containing no white pigment and inorganic particles and having an intrinsic viscosity of 0.62 dl / g (c) as a film raw material. A mixture of 50.0% by mass of particles and 0.1% by mass of an optical brightener (manufactured by Eastman Chemical Co., Ltd.) was supplied to a vent type twin screw extruder and pre-kneaded. Next, this molten resin was continuously supplied to a bent type single-screw kneader, kneaded and extruded, and the obtained strand was cooled and cut to produce a titanium dioxide-containing master pellet (a).

  Next, polyethylene terephthalate resin pellets (b) having an intrinsic viscosity of 0.62 dl / g containing 0.7% by mass of silica particles having an average particle diameter of 1.8 μm added by a conventional addition method during polymerization were produced.

  75% by mass of polyethylene terephthalate resin (c) having an intrinsic viscosity of 0.62 dl / g and containing no white pigment and inorganic particles, and 25% by mass of the above-mentioned master pellet (a) containing titanium dioxide particles (white pigment), Vacuum drying was performed at 140 ° C. for 8 hours to obtain a film raw material (I). In addition, 30% by mass of the titanium dioxide-containing master pellet (a) and 70% by mass of the silica particle (inorganic particle) -containing pellet (b) are mixed in a pellet and vacuum dried at 140 ° C. for 8 hours to obtain a film raw material (II) It was.

(Manufacture of laminated film)
The film raw materials are respectively supplied to different extruders, and a layer (B layer) composed of the raw material (I) and a layer (A layer) composed of the raw material (II) are fed into a layer A / layer B / layer A using a feed block. The layers were laminated in the molten state in this order. This molten resin was coextruded from a T-die onto a rotating cooling metal roll adjusted to 25 ° C. The discharge rate of each extruder is adjusted so that the thickness ratio of each layer is 10:80:10, and it is rapidly cooled and solidified on a chill roll having a surface temperature of 40 ° C. A regular unstretched sheet was obtained.

  The obtained unstretched sheet was stretched 3.1 times at 95 ° C. in the machine direction between the heating roll and the cooling roll.

  Subsequently, the aqueous coating liquid A shown above was applied to one side of the film by roll coating on the obtained uniaxially stretched film, and dried at 130 ° C. for 3 seconds to remove moisture.

After that, it is guided to a tenter while continuously gripping the end with a clip, heated at a setting of 120 ° C. and stretched to 3.7 times, and subjected to heat treatment at 230 ° C. for 5 seconds while fixing the width. By relaxing 5% in the width direction at 0 ° C., a white laminated polyester film having an easily adhesive layer with a coating thickness of 0.2 μm was obtained. The apparent density of the base film was 1.47 g / cm ³ .

  The evaluation results of the obtained laminated polyester film are shown in Table 1.

(Preparation of coating solution B)
The ratio of the solid content of the polyester graft copolymer (a1) and the water dispersible polycarbonate urethane resin (b1) obtained above is polyester graft copolymer / polyurethane resin (mass ratio) = 80/20. In addition, the block isocyanate compound having an isocyanate group content (regenerated NCO) of 5.4% by mass with respect to 100 parts by mass of the total amount of the polyester-based graft copolymer and the polyurethane resin is mixed so as to be 20 parts by mass. The total resin solid content concentration is 12.0% by mass, and the silica particles having an average particle size of 1.0 μm are 0.44% by mass with respect to the total resin and the silica particles having an average particle size of 0.1 μm are based on the total resin. In order to contain 10% by mass, it was diluted with a mixed solvent of water / isopropyl alcohol (= 65/35; mass ratio) to obtain an aqueous coating agent.

Example 2
In Example 1, a laminated polyester film having a coating thickness of 0.2 μm was obtained in the same manner as in Example 1 except that the coating liquid A was replaced with the coating liquid B. The characteristics and evaluation results of the obtained film are shown in Table 1.

(Preparation of coating solution C)
The ratio of the solid content of the copolyester resin liquid (a1) and polyurethane resin (b1) obtained above is copolyester resin / polyurethane resin (mass ratio) = 70/30, and the copolyester resin and Mixing so that the isocyanate group content (regenerated NCO) is 5.4% by mass with respect to a total amount of 100 parts by mass of the polyurethane resin is 20 parts by mass of the blocked isocyanate compound, and the total resin solid content concentration is 12.0% by mass. %, Was diluted with a mixed solvent of water / isopropyl alcohol (= 65/35; mass ratio) to obtain an aqueous coating agent.

Example 3
A laminated polyester film having a coating thickness of 0.2 μm was obtained in the same manner as in Example 2 except that the coating liquid B was replaced with the coating liquid C in Example 2. The characteristics and evaluation results of the obtained film are shown in Table 1.

(Preparation of coating solution D)
The ratio of the solid content of the copolyester resin liquid (a1) and polyurethane resin (b1) obtained above is copolyester resin / polyurethane resin (mass ratio) = 40/60, and the copolyester resin and Mixing so that the isocyanate group content (regenerated NCO) is 5.4% by mass with respect to a total amount of 100 parts by mass of the polyurethane resin is 20 parts by mass of the blocked isocyanate compound, and the total resin solid content concentration is 12.0% by mass. %, Particles having an average particle diameter of 1.0 μm as 0.44% by mass with respect to the total resin and 10% by mass of silica particles with an average particle diameter of 0.1 μm with respect to the total resin as water / It was diluted with a mixed solvent of isopropyl alcohol (= 65/35; mass ratio) to obtain an aqueous coating agent.

Example 4
In Example 2, a laminated polyester film having a coating thickness of 0.2 μm was obtained in the same manner as in Example 2 except that the coating liquid B was replaced with the coating liquid D. The characteristics and evaluation results of the obtained film are shown in Table 1.

(Preparation of coating solution E)
The ratio of the solid content of the copolyester resin liquid (a1) and polyurethane resin (b1) obtained above is copolyester resin / polyurethane resin (mass ratio) = 30/70, and the copolyester resin and Mixing so that the isocyanate group content (regenerated NCO) is 5.4% by mass with respect to a total amount of 100 parts by mass of the polyurethane resin is 20 parts by mass of the blocked isocyanate compound, and the total resin solid content concentration is 12.0% by mass. %, Particles having an average particle diameter of 1.0 μm as 0.44% by mass with respect to the total resin and 10% by mass of silica particles with an average particle diameter of 0.1 μm with respect to the total resin as water / It was diluted with a mixed solvent of isopropyl alcohol (= 65/35; mass ratio) to obtain an aqueous coating agent.

Example 5
In Example 2, a laminated polyester film having a coating thickness of 0.2 μm was obtained in the same manner as in Example 2 except that the coating liquid B was replaced with the coating liquid E. The characteristics and evaluation results of the obtained film are shown in Table 1.

(Preparation of coating solution F)
The ratio of the solid content of the copolymerized polyester resin liquid (a1) and polyurethane resin (b1) obtained above is copolymerized polyester resin / polyurethane resin (mass ratio) = 10/90, and the copolymerized polyester resin and Mixing so that the isocyanate group content (regenerated NCO) is 5.4% by mass with respect to a total amount of 100 parts by mass of the polyurethane resin is 20 parts by mass of the blocked isocyanate compound, and the total resin solid content concentration is 12.0% by mass. %, Particles having an average particle diameter of 1.0 μm as 0.44% by mass with respect to the total resin and 10% by mass of silica particles with an average particle diameter of 0.1 μm with respect to the total resin as water / It was diluted with a mixed solvent of isopropyl alcohol (= 65/35; mass ratio) to obtain an aqueous coating agent.

Example 6
In Example 2, a laminated polyester film having a coating thickness of 0.2 μm was obtained in the same manner as in Example 2 except that the coating liquid B was replaced with the coating liquid F. The characteristics and evaluation results of the obtained film are shown in Table 1.

(Preparation of coating solution G)
The ratio of the solid content of the copolyester resin liquid (a1) obtained above and a polyurethane resin having a glass transition point of 85 ° C. (catalog value) (trade name Takelac W615, manufactured by Mitsui Takeda Chemical Co., Ltd.) is a copolyester resin. / Block polyurethane resin (mass ratio) = 80/20 and the isocyanate group content (regenerated NCO) is 5.4% by mass with respect to 100 parts by mass of the total amount of the copolyester resin and polyurethane resin The compound was mixed so as to be 20 parts by mass, the total resin solid content concentration was 12.0% by mass, and particles having a silica particle average particle size of 1.0 μm were 0.44% by mass with respect to the total resin and the average particle size was 0. In a mixed solvent of water / isopropyl alcohol (= 65/35; mass ratio) so as to contain 10% by mass of silica particles of 1 μm with respect to the total resin This was used as a water-based coating agent.

Example 7
In Example 2, a laminated polyester film having a coating thickness of 0.2 μm was obtained in the same manner as in Example 2 except that the coating liquid B was replaced with the coating liquid G. The characteristics and evaluation results of the obtained film are shown in Table 1.

(Preparation of coating solution H)
The ratio of the solid content of the copolyester resin liquid (a1) obtained above and a polyurethane resin having a glass transition point of 85 ° C. (catalog value) (trade name Takelac W615, manufactured by Mitsui Takeda Chemical Co., Ltd.) is a copolyester resin. / Polyurethane resin (mass ratio) = 80/20 and 20 parts by mass of a polyisocyanate compound having an isocyanate group content of 12.4% by mass based on 100 parts by mass of the total amount of the copolyester resin and the polyurethane resin Silica having a total resin solid content concentration of 12.0% by mass and silica particles having an average particle size of 1.0 μm as a particle and 0.44% by mass with respect to the total resin and an average particle size of 0.1 μm. Dilute with a mixed solvent of water / isopropyl alcohol (= 65/35; mass ratio) so as to contain 10% by mass of the particles with respect to the total resin. A cloth was used.

Example 8
In Example 2, a laminated polyester film having a coating thickness of 0.2 μm was obtained in the same manner as in Example 2 except that the coating liquid B was replaced with the coating liquid H. The characteristics and evaluation results of the obtained film are shown in Table 1.

(Preparation of coating liquid I)
The ratio of the solid content of the copolyester resin liquid (a1) obtained above and a polyurethane resin having a glass transition point of 85 ° C. (catalog value) (trade name Takelac W615, manufactured by Mitsui Takeda Chemical Co., Ltd.) is a copolyester resin. / Polyurethane resin (mass ratio) = 80/20, and the isocyanate group content (regenerated NCO) is 7% by mass with respect to 100 parts by mass of the total amount of the copolyester resin and the polyurethane resin. The total resin solid content concentration is 12.0% by mass, and the silica particles have an average particle size of 1.0 μm as particles, 0.44% by mass and the average particle size of 0.1 μm. Diluted with a mixed solvent of water / isopropyl alcohol (= 65/35; mass ratio) so as to contain 10% by mass of silica particles based on the total resin. Water-based coating agent.

Example 9
In Example 2, a laminated polyester film having a coating thickness of 0.2 μm was obtained in the same manner as in Example 2 except that the coating liquid B was replaced with the coating liquid I. The characteristics and evaluation results of the obtained film are shown in Table 1.

(Preparation of coating solution J)
The ratio of the solid content of the copolyester resin liquid (a1) obtained above and a polyurethane resin having a glass transition point of 85 ° C. (catalog value) (trade name Takelac W615, manufactured by Mitsui Takeda Chemical Co., Ltd.) is a copolyester resin. / Block polyurethane resin (mass ratio) = 80/20, and the isocyanate group content (regenerated NCO) is 4.5 mass% with respect to 100 mass parts of the total amount of the copolyester resin and polyurethane resin The compound was mixed so as to be 20 parts by mass, the total resin solid content concentration was 12.0% by mass, and particles having a silica particle average particle size of 1.0 μm were 0.44% by mass with respect to the total resin and the average particle size was 0. In a mixed solvent of water / isopropyl alcohol (= 65/35; mass ratio) so as to contain 10% by mass of silica particles of 1 μm with respect to the total resin This was used as a water-based coating agent.

Example 10
In Example 2, a laminated polyester film having a coating thickness of 0.2 μm was obtained in the same manner as in Example 2 except that the coating liquid B was replaced with the coating liquid J. The characteristics and evaluation results of the obtained film are shown in Table 1.

(Preparation of coating solution K)
The ratio of the solid content of the copolyester resin liquid (a1) obtained above and a polyurethane resin having a glass transition point of 85 ° C. (catalog value) (trade name Takelac W615, manufactured by Mitsui Takeda Chemical Co., Ltd.) is a copolyester resin. / Block polyurethane resin (mass ratio) = 80/20 and the isocyanate group content (regenerated NCO) is 3.0% by mass with respect to 100 parts by mass of the total amount of the copolyester resin and the polyurethane resin. The compound was mixed so as to be 20 parts by mass, the total resin solid content concentration was 12.0% by mass, and particles having a silica particle average particle size of 1.0 μm were 0.44% by mass with respect to the total resin and the average particle size was 0. In a mixed solvent of water / isopropyl alcohol (= 65/35; mass ratio) so as to contain 10% by mass of silica particles of 1 μm with respect to the total resin This was used as a water-based coating agent.

Example 11
In Example 2, a laminated polyester film having a coating thickness of 0.2 μm was obtained in the same manner as in Example 2 except that the coating liquid B was replaced with the coating liquid K. The characteristics and evaluation results of the obtained film are shown in Table 1.

(Preparation of coating liquid L)
The ratio of the solid content of the copolyester resin liquid (a1) and polyurethane resin (b1) obtained above is copolyester resin / polyurethane resin (mass ratio) = 80/20, and the copolyester resin and Mixing so that the isocyanate group content is 40 parts by mass with respect to the total amount of polyurethane resin of 100 parts by mass, and the total resin solid content concentration is 12.0% by mass as particles. Water / isopropyl alcohol so that silica particles having an average particle diameter of 1.0 μm are contained in an amount of 0.44% by mass based on the total resin and silica particles having an average particle diameter of 0.1 μm are included in the total resin by 10% by mass. Was diluted with a mixed solvent (= 65/35; mass ratio) to obtain an aqueous coating agent.

Example 12
In Example 2, a laminated polyester film having a coating thickness of 0.2 μm was obtained in the same manner as in Example 2 except that the coating liquid B was replaced with the coating liquid L. The characteristics and evaluation results of the obtained film are shown in Table 1.

(Preparation of coating solution M)
The ratio of the solid content of the copolyester resin liquid (a1) and polyurethane resin (b1) obtained above is copolyester resin / polyurethane resin (mass ratio) = 80/20, and the copolyester resin and Mixing so that the isocyanate group content is 5.4% by mass with respect to the total amount of 100 parts by mass of the polyurethane resin is 25 parts by mass of the blocked isocyanate compound, and the total resin solid content concentration is 12.0% by mass as particles. Water / isopropyl alcohol so that silica particles having an average particle diameter of 1.0 μm are contained in an amount of 0.44% by mass based on the total resin and silica particles having an average particle diameter of 0.1 μm are included in the total resin by 10% by mass. Was diluted with a mixed solvent (= 65/35; mass ratio) to obtain an aqueous coating agent.

Example 13
In Example 2, a laminated polyester film having a coating thickness of 0.2 μm was obtained in the same manner as in Example 2 except that the coating liquid B was replaced with the coating liquid M. Table 2 shows the properties and evaluation results of the obtained film.

(Preparation of coating solution N)
The ratio of the solid content of the copolyester resin liquid (a1) and polyurethane resin (b1) obtained above is copolyester resin / polyurethane resin (mass ratio) = 80/20, and the copolyester resin and Mixing so that the isocyanate group content is 8 parts by mass with respect to 100 parts by mass of the total amount of polyurethane resin, and the total resin solid content concentration is 12.0% by mass as particles. Water / isopropyl alcohol so that silica particles having an average particle diameter of 1.0 μm are contained in an amount of 0.44% by mass based on the total resin and silica particles having an average particle diameter of 0.1 μm are included in the total resin by 10% by mass. Was diluted with a mixed solvent (= 65/35; mass ratio) to obtain an aqueous coating agent.

Example 14
In Example 2, a laminated polyester film having a coating thickness of 0.2 μm was obtained in the same manner as in Example 2 except that the coating liquid B was replaced with the coating liquid N. The characteristics and evaluation results of the obtained film are shown in Table 1.

(Preparation of coating solution O)
The ratio of the solid content of the copolyester resin liquid (a1) and polyurethane resin (b1) obtained above is copolyester resin / polyurethane resin (mass ratio) = 80/20, and the copolyester resin and Mixing so that the isocyanate group content is 5 parts by mass with respect to 100 parts by mass of the total amount of the polyurethane resin, and the total resin solid content concentration is 12.0% by mass as particles. Water / isopropyl alcohol so that silica particles having an average particle diameter of 1.0 μm are contained in an amount of 0.44% by mass based on the total resin and silica particles having an average particle diameter of 0.1 μm are included in the total resin by 10% by mass. Was diluted with a mixed solvent (= 65/35; mass ratio) to obtain an aqueous coating agent.

Example 15
In Example 2, a laminated polyester film having a coating thickness of 0.2 μm was obtained in the same manner as in Example 2 except that the coating liquid B was replaced with the coating liquid O. The characteristics and evaluation results of the obtained film are shown in Table 1.

(Preparation of coating solution P)
The ratio of the solid content of the copolyester resin liquid (a1) and polyurethane resin (b1) obtained above is copolyester resin / polyurethane resin (mass ratio) = 80/20, and the copolyester resin and Mixing so that the isocyanate group content is 20 parts by mass with respect to 100 parts by mass of the total amount of the polyurethane resin, and the total resin solid content concentration is 12.0% by mass as particles. Water / Isople so that silica particles having an average particle diameter of 1.4 μm are contained in an amount of 3.0% by mass with respect to the total resin and silica particles having an average particle diameter of 0.2 μm in an amount of 0.02% by mass with respect to the total resin. It was diluted with a mixed solvent of pill alcohol (= 65/35; mass ratio) to obtain an aqueous coating agent.

Example 16
In Example 2, a laminated polyester film having a coating thickness of 0.2 μm was obtained in the same manner as in Example 2 except that the coating liquid B was replaced with the coating liquid P. The characteristics and evaluation results of the obtained film are shown in Table 1.

Example 17
A laminated polyester film similar to that of Example 1 was obtained except that the coating thickness of the easy adhesion layer was 0.4 μm. The characteristics and evaluation results of the obtained film are shown in Table 1.

Example 18
A laminated polyester film similar to Example 1 was obtained except that the coating thickness of the easy adhesion layer was 0.15 μm. The characteristics and evaluation results of the obtained film are shown in Table 1.

Example 19
A laminated polyester film similar to that of Example 1 was obtained except that the coating thickness of the easy adhesion layer was 0.10 μm. The characteristics and evaluation results of the obtained film are shown in Table 1.

Example 20
A laminated polyester film similar to Example 1 was obtained except that the coating thickness of the easy adhesion layer was 0.07 μm. Table 2 shows the properties and evaluation results of the obtained film.

(Coating solution Q preparation)
The ratio of the solid content of the copolyester resin liquid (a1) and polyurethane resin (b1) obtained above is copolyester resin / polyurethane resin (mass ratio) = 80/20, and the copolyester resin and Mixing so that the isocyanate group content is 5.4% by mass with respect to 100 parts by mass of the total amount of the polyurethane resin, and mixing with 20 parts by mass of the blocked isocyanate compound, polystyrene sulfonate ammonium salt, antistatic agent having a molecular weight of 10,000 Mixing so that the content is 1.5% by mass, the total resin solid content concentration is 12.0% by mass, and the particles having silica average particle diameter of 1.4 μm are 3.0% by mass with respect to the total resin. And a mixed solvent of water / isopropyl alcohol (= 65 /%) so as to contain 0.02% by mass of silica particles having an average particle size of 0.2 μm with respect to the total resin. 5; and an aqueous coating agent was diluted in a mass ratio).

Example 21
In Example 2, a laminated polyester film having a coating thickness of 0.2 μm was obtained in the same manner as in Example 2 except that the coating liquid B was replaced with the coating liquid Q. The characteristics and evaluation results of the obtained film are shown in Table 1. When offset printing was performed on the film obtained in this example, there was little blurring due to printing, and the printability was good.

(Coating solution R preparation)
The ratio of the solid content of the copolyester resin liquid (a1) and polyurethane resin (b1) obtained above is copolyester resin / polyurethane resin (mass ratio) = 100/0, and copolyester resin 100 It is mixed so that the isocyanate group content is 5.4% by mass relative to 20 parts by mass of the blocked isocyanate compound, and the total resin solid content concentration is 12.0% by mass. A mixed solvent of water / isopropyl alcohol (= 65) so as to contain 0.4 .mu.m of 0.0.mu.m and 10% by mass of silica particles having an average particle size of 0.1 .mu.m with respect to the total resin. / 35; mass ratio) to obtain an aqueous coating agent.

Comparative Example 1
In Example 2, a laminated polyester film having a coating thickness of 0.2 μm was obtained in the same manner as in Example 2 except that the coating liquid B was replaced with the coating liquid R. The characteristics and evaluation results of the obtained film are shown in Table 1.

(Preparation of coating solution S)
The ratio of the solid content of the copolyester resin liquid (a1) and polyurethane resin (b1) obtained above is copolyester resin / polyurethane resin (mass ratio) = 0/100, and copolyester resin 100 It is mixed so that the isocyanate group content is 5.4% by mass based on 20 parts by mass of the blocked isocyanate compound, and the total resin solid content concentration is 3.8% by mass. A mixed solvent of water / isopropyl alcohol (= 65) so as to contain 0.4 .mu.m of 0.0.mu.m and 10% by mass of silica particles having an average particle size of 0.1 .mu.m with respect to the total resin. / 35; mass ratio) to obtain an aqueous coating agent.

Comparative Example 2
In Example 2, a laminated polyester film having a coating thickness of 0.2 μm was obtained in the same manner as in Example 2 except that the coating liquid B was replaced with the coating liquid S. The characteristics and evaluation results of the obtained film are shown in Table 1.

(Preparation of coating solution T)
The ratio of the solid content of the copolymerized polyester resin liquid (a1) and polyurethane resin (b1) obtained above is copolymerized polyester resin / polyurethane resin (mass ratio) = 80/20, and the total resin solid content concentration is 3. 0.84% by mass, 0.44% by mass of silica particles having an average particle size of 1.0 μm as particles and 10% by mass of silica particles having an average particle size of 0.1 μm with respect to all resins The mixture was diluted with a mixed solvent of water / isopropyl alcohol (= 65/35; mass ratio) to obtain an aqueous coating agent.

Comparative Example 3
In Example 2, a laminated polyester film having a coating thickness of 0.2 μm was obtained in the same manner as in Example 2 except that the coating liquid B was replaced with the coating liquid T. Table 2 shows the properties and evaluation results of the obtained film.

(Preparation of coating solution U)
The proportion of the copolymerized polyester resin liquid (a1) obtained above and the temperature of 35 ° C. (catalog value) polyurethane resin (manufactured by Mitsui Takeda Chemicals Co., Ltd .: trade name Takelac W511) is a copolymerized polyester resin / polyurethane resin (mass Ratio) = 80/20, and mixed so that the isocyanate group content is 5.4% by mass and the blocked isocyanate compound is 20 parts by mass with respect to 100 parts by mass of the total amount of the copolyester resin and the polyurethane resin. The total resin solids concentration of 3.8% by mass and the silica particles having an average particle size of 1.0 μm as the particles are 0.44% by mass relative to the total resin, and the silica particles having an average particle size of 0.1 μm are used as the total resin. On the other hand, it was diluted with a mixed solvent of water / isopropyl alcohol (= 65/35; mass ratio) so as to contain 10% by mass to obtain an aqueous coating agent.

Comparative Example 4
In Example 2, a laminated polyester film having a coating thickness of 0.2 μm was obtained in the same manner as in Example 2 except that the coating liquid B was replaced with the coating liquid U. The characteristics and evaluation results of the obtained film are shown in Table 1.

(Preparation of coating solution V)
Preparation of Copolyester Resin Coating solution V was prepared according to the following method. A reaction vessel was charged with 95 parts by weight of dimethyl terephthalate, 95 parts by weight of dimethyl isophthalate, 35 parts by weight of ethylene glycol, 145 parts by weight of neopentyl glycol, 0.1 part by weight of zinc acetate and 0.1 part by weight of antimony trioxide. The transesterification was carried out over 3 hours. Next, 6.0 parts by mass of 5-sodium sulfoisophthalic acid was added, and esterification was performed at 240 ° C. over 1 hour, and then at 250 ° C. under reduced pressure (10 to 0.2 mmHg) over 2 hours. A polycondensation reaction was performed to obtain a copolymerized polyester resin (a2) having a number average molecular weight of 19,500.
Preparation of polyurethane resin aqueous solution 100 parts by mass of polyester diol (OHV: 2000 eq / ton) having a composition of adipic acid // 1.6-hexanediol / neopentyl glycol (molar ratio: 4 // 2/3), After 41.4 parts by mass of diisocyanate was mixed and reacted at 80 to 90 ° C. for 1 hour under a nitrogen stream, the mixture was cooled to 60 ° C., 70 parts by mass of tetrahydrofuran was added and dissolved, and a urethane prepolymer solution (NCO / OH ratio: 2.2, free isocyanate group: theoretical value 3.56% by mass, measured value 3.30% by mass). Subsequently, the urethane prepolymer solution was brought to 40 ° C., then, 45.5 parts by mass of a 20% by mass aqueous sodium bisulfite solution was added, and the mixture was reacted at 40-50 ° C. for 30 minutes while vigorously stirring. After confirming the disappearance of the free isocyanate group content (in terms of solid content), it was diluted with emulsified water to obtain a polyurethane resin aqueous solution (b2) having a solid content of 20% by mass.
7.5 parts by mass of a 30% by mass aqueous dispersion of the obtained copolyester resin (a2), 11.3 parts by mass of the polyurethane resin aqueous solution (b2), and 0.03 of the catalyst (dibutyltin laurate). 39.8 parts by mass of water, 39.8 parts by mass of water, and 37.4 parts by mass of isopropyl alcohol were mixed. Further, 0.6 part by mass of a 10% by mass aqueous solution of a nonionic surfactant, 2.3 parts by mass of a 20% by mass aqueous dispersion of colloidal silica (average particle size 0.04 μm) as particles, and then 5% by mass The pH of the coating solution was adjusted to 6.2 with an aqueous sodium bicarbonate solution, and the solution was precisely filtered through a felt-type polypropylene filter having a filtration particle size (initial filtration efficiency: 95%) of 10 μm to prepare coating solution V.

Comparative Example 5
In Example 2, a laminated polyester film having a coating thickness of 0.2 μm was obtained in the same manner as in Example 2 except that the coating liquid B was replaced with the coating liquid V. Table 1 shows the properties and evaluation results of the obtained single-layer film.

(Preparation of coating liquid W)
The polyester-based graft copolymer (a1) obtained above has a solid content ratio of an ether-based polyurethane resin (trade name Takelac W6020, manufactured by Mitsui Takeda Chemical Co., Ltd.) having a glass transition point of 90 ° C. (catalog value). System graft copolymer / polyurethane resin (mass ratio) = 80/20, and the isocyanate group content (regenerated NCO) is 5. with respect to 100 parts by mass of the total amount of the polyester system graft copolymer and polyurethane resin. The block isocyanate compound of 4% by mass is mixed so as to be 20 parts by mass, the total resin solid content concentration is 3.8% by mass, and the silica particles have an average particle diameter of 1.0 μm as the total resin. A mixture of water / isopropyl alcohol so as to contain 44% by mass and 10% by mass of silica particles having an average particle size of 0.1 μm with respect to the total resin. It diluted with the mixed solvent (= 65/35; mass ratio), and was set as the water-system coating agent.

Comparative Example 6
In Example 2, a laminated polyester film having a coating thickness of 0.2 μm was obtained in the same manner as in Example 2 except that the coating liquid B was replaced with the coating liquid W. Table 1 shows the properties and evaluation results of the obtained single-layer film.

(Preparation of coating solution X)
The polyester-based graft copolymer (a1) obtained above and the solid content of the ester-based polyurethane resin (trade name Takelac W5030, manufactured by Mitsui Takeda Chemical Co., Ltd.) having a glass transition point of 85 ° C. (catalog value) are polyester. System graft copolymer / polyurethane resin (mass ratio) = 80/20, and the isocyanate group content (regenerated NCO) is 5. with respect to 100 parts by mass of the total amount of the polyester system graft copolymer and polyurethane resin. The block isocyanate compound of 4% by mass is mixed so as to be 20 parts by mass, the total resin solid content concentration is 3.8% by mass, and the silica particles have an average particle diameter of 1.0 μm as the total resin. A mixture of water / isopropyl alcohol so as to contain 44% by mass and 10% by mass of silica particles having an average particle size of 0.1 μm with respect to the total resin. It diluted with the mixed solvent (= 65/35; mass ratio), and was set as the water-system coating agent.

Comparative Example 7
In Example 2, a laminated polyester film having a coating thickness of 0.2 μm was obtained in the same manner as in Example 2 except that the coating liquid B was replaced with the coating liquid X. Table 1 shows the properties and evaluation results of the obtained single-layer film.

Example 22
In the preparation of the coating liquid A, a coating liquid (Y) in which a melamine compound (Beccamin M-3 solid content concentration 60% manufactured by DIC) was changed to 16.7% by mass in the solid content instead of the blocked isocyanate compound was used. Except for the above, a laminated polyester film having a coating thickness of 0.2 μm was obtained in the same manner as in Example 1. Table 1 shows the properties and evaluation results of the obtained single-layer film.

  The white laminated polyester film according to the present invention is excellent in moldability and adhesiveness, particularly adhesiveness under heat and humidity resistance, and can be applied to a wide range of applications. Therefore, it is suitable as various information recording materials and printing materials, particularly as a base material for IC cards and a base material for IC tags.

Claims (5)

A laminated polyester film having an easy-adhesion layer on at least one side of a base film comprising a polyester film containing a white pigment and / or inorganic particles,
The easy-adhesion layer includes a polyester-based graft copolymer and a polycarbonate-based polyurethane,
The polyester-based graft copolymer is obtained by grafting a polymerizable unsaturated monomer containing an acid anhydride having at least one double bond to a hydrophobic copolymerized polyester resin.
And the glass transition point (Tig) of an easily bonding layer is 30 to 55 degreeC,
White laminated polyester film. The blending ratio of the polyester-based graft copolymer and the polycarbonate-based polyurethane in the easy-adhesion layer is polyester-based graft copolymer / polycarbonate-based polyurethane (mass ratio) = 80/20 to 30/70,
And the white laminated polyester film of Claim 1 containing 5-40 mass parts crosslinking agent with respect to 100 mass parts of total amounts of a polyester-type graft copolymer and a polycarbonate-type polyurethane. The white laminated polyester film according to claim 2, wherein the crosslinking agent is a blocked isocyanate crosslinking agent. The white laminated polyester film according to claim 3, wherein a content of the regenerated isocyanate group in the blocked isocyanate crosslinking agent is 3.0 to 15.0 mass%. 5. The white laminated polyester film according to claim 1, wherein a surface specific resistance value of the surface of the easy adhesion layer at 25 ° C. and 65% RH is 1 × 10 ⁶ to 10 ¹³ Ω / □.