JP2022179513A - heat shrinkable multilayer film - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a heat shrinkable film which can suppress deterioration of feedability due to sticking of films with each other and adhesion of labels with each other after mounting the film on the label and can prevent trapping failure by decreasing flying of ink at the time of overprinting.

SOLUTION: Provided is a heat shrinkable multilayer film comprising front and back layers and a middle layer which are laminated with adhesive layers interposed therebetween. The front and back layers include a polyester resin and organic fine particles, the middle layer includes a polystyrene resin, and a content of the organic fine particles relative to 100 pts.wt. of the polyester resin is 0.055 to 0.145 pt.wt.

SELECTED DRAWING: None

COPYRIGHT: (C)2023,JPO&INPIT

Description

The present invention can suppress the deterioration of feeding performance due to adhesion between films and the adhesion of labels after label attachment, reduce ink skipping during overprinting, and prevent trapping defects. It relates to a heat-shrinkable film.

2. Description of the Related Art In recent years, many containers such as PET bottles and metal cans are provided with a heat-shrinkable label obtained by printing a heat-shrinkable film made of a heat-shrinkable resin.
Heat-shrinkable films are required to have various properties such as heat resistance, solvent resistance, perforation cuttability, etc., in addition to low-temperature shrinkability.

In general, heat-shrinkable film is wound into a roll, cut into a predetermined size, printed, sealed with a solvent, and attached to a container by heat shrinkage. Due to the close contact, there is a problem that the film is torn when it is fed out and the films cannot be separated from each other. In addition, when the label is attached to the container due to heat shrinkage, or when the container is stored with the label attached, the labels adhere to each other and cannot be peeled off, or the label is peeled off from the container.

Therefore, in order to prevent the slipperiness of the film and adhesion between films, a method of adding an anti-blocking agent such as silica or talc is used.
However, although these anti-blocking agents roughen the film surface to develop slipperiness and anti-blocking properties, there is a problem that the film is stained and causes poor appearance.

In contrast, Patent Document 1 proposes a shrink film containing rubber-modified styrene, a lubricant, and inorganic or organic fine particles in order to improve blocking resistance and natural shrinkage resistance under long-term storage. It is

JP-A-2002-161147

However, although such a shrink film can prevent the film from sticking to each other and is easy to feed out, there is a problem in that a trapping defect such as ink splattering occurs when the label is printed.

The present invention can suppress the deterioration of feeding performance due to adhesion between films and the adhesion of labels after label attachment, reduce ink skipping during overprinting, and prevent trapping defects. An object of the present invention is to provide a heat-shrinkable film.

The present invention is a heat-shrinkable multilayer film comprising front and back layers and an intermediate layer laminated via an adhesive layer, wherein the front and back layers contain a polyester resin and organic fine particles, and the intermediate layer is a heat-shrinkable multi-layer film containing a polystyrene resin and containing 0.055 to 0.145 parts by weight of the organic fine particles with respect to 100 parts by weight of the polyester resin.
The present invention will be described in detail below.

The present inventors have found that a heat-shrinkable film having front and back layers containing polyester resin and organic fine particles in a predetermined ratio not only has excellent film feeding properties and can prevent labels from sticking to each other, The present inventors have found that it is possible to reduce ink splattering and prevent trapping defects even in overprinting, and have completed the present invention.

The heat-shrinkable multilayer film of the present invention has front and back layers, an intermediate layer and an adhesive layer.
In addition, in this specification, the front and back layers mean both the surface layer and the back layer.

(front and back layers)
The front and back layers contain a polyester-based resin.
Examples of the polyester-based resin include those obtained by condensation polymerization of a dicarboxylic acid component and a diol component.
In particular, the dicarboxylic acid component is preferably an aromatic polyester resin containing 55 mol % or more of terephthalic acid in 100 mol % of the dicarboxylic acid component.
Furthermore, as the dicarboxylic acid component, in addition to the above terephthalic acid, o-phthalic acid, isophthalic acid, succinic acid, adipic acid, sebacic acid, azelaic acid, octylsuccinic acid, cyclohexanedicarboxylic acid, naphthalenedicarboxylic acid, fumaric acid, Maleic acid, itaconic acid, decamethylenecarboxylic acid, anhydrides and lower alkyl esters thereof, and the like can be included.

The diol component is not particularly limited, and examples include ethylene glycol, 1,3-propanediol, 1,4-butanediol, diethylene glycol, 1,5-pentanediol, 1,6-hexanediol, dipropylene glycol, triethylene glycol, tetraethylene glycol, 1,2-propanediol, 1,3-butanediol, 2,3-butanediol, neopentyl glycol (2,2-dimethylpropane-1,3-diol), 1,2 -hexanediol, 2,5-hexanediol, 2-methyl-2,4-pentanediol, 3-methyl-1,3-pentanediol, 2-ethyl-1,3-hexanediol, polytetramethylene ether glycol, etc. 2,2-bis(4-hydroxycyclohexyl)propane, alkylene oxide adduct of 2,2-bis(4-hydroxycyclohexyl)propane, 1,4-cyclohexanediol, 1,4-cyclohexanediol Alicyclic diols, such as methanol, etc. are mentioned.

Among the polyester-based resins, those containing a component derived from terephthalic acid as a dicarboxylic acid component and a component derived from ethylene glycol and/or 1,4-cyclohexanedimethanol as a diol component. preferable.
By using such an aromatic polyester-based random copolymer resin, excellent heat shrinkability can be imparted to the heat shrinkable film.
When it is desired to further increase the heat shrinkability, the content of the component derived from ethylene glycol is 60 to 80 mol% and the content of the component derived from 1,4-cyclohexanedimethanol is 60 to 80 mol% out of 100 mol% of the diol component. It is preferable to use one having a content of 10 to 40 mol %.

Such an aromatic polyester-based random copolymer resin may further contain 0 to 30 mol%, preferably 1 to 25 mol%, more preferably 2 to 20 mol% of a component derived from diethylene glycol. By using diethylene glycol, the tensile elongation at break in the main shrinkage direction of the heat-shrinkable film is increased, and when the perforations are torn, delamination can be prevented and only the inner surface side remains in the container. . When the diethylene glycol-derived component is 30 mol% or less, the low-temperature shrinkability of the heat-shrinkable film can be reduced, and wrinkles can be prevented when the film is attached to a container.

The polyester resin containing a component derived from terephthalic acid as the dicarboxylic acid component may also contain a component derived from 1,4-butanediol as the diol component. Such polyester resins are generally called polybutylene terephthalate resins.
The polybutylene terephthalate resin contains a component derived from terephthalic acid as the dicarboxylic acid component, and an aromatic polyester random containing a component derived from ethylene glycol and 1,4-cyclohexanedimethanol as the diol component. It is preferably used in combination with a copolymer resin. By using such a mixed resin, it is possible to impart a more excellent finish.

As the polybutylene terephthalate-based resin, in addition to a polybutylene terephthalate-based resin consisting only of a component derived from terephthalic acid and a component derived from 1,4-butanediol, a dicarboxylic acid component other than a component derived from terephthalic acid and / Alternatively, it may be a polybutylene terephthalate-based resin containing a diol component other than the component derived from 1,4-butanediol.
The content of the dicarboxylic acid component other than the component derived from terephthalic acid is preferably 40 mol % or less in 100 mol % of the dicarboxylic acid component.
When it is 40 mol % or less, the heat resistance of the polybutylene terephthalate-based resin can be improved. The content of the diol component other than the component derived from 1,4-butanediol is preferably 10 mol % or less in 100 mol % of the diol component. When it is 10 mol % or less, the heat resistance of the polybutylene terephthalate-based resin can be improved.

Although the content of the polybutylene terephthalate-based resin in the front and back layers is not particularly limited, it is preferably 30% by weight or less.
If it is 30% by weight or less, natural shrinkage can be suppressed, and a decrease in film rigidity can be prevented.

The preferable lower limit of the glass transition temperature of the polyester-based resin constituting the front and back layers is 55°C, and the preferable upper limit thereof is 95°C.
When the glass transition temperature is 55° C. or higher, the shrinkage initiation temperature of the heat-shrinkable film can be made sufficiently high, and natural shrinkage can be suppressed. When the glass transition temperature is 95° C. or lower, the low-temperature shrinkability and shrink finish of the heat-shrinkable film can be improved, and deterioration of the low-temperature shrinkability over time can be suppressed.
A more preferable lower limit of the glass transition temperature is 60°C, and a more preferable upper limit is 90°C.
The glass transition temperature can be measured with a differential scanning calorimeter (DSC).

The preferred lower limit of the tensile modulus of the polyester resin constituting the front and back layers is 1000 MPa, and the preferred upper limit is 4000 MPa.
When the tensile modulus is 1000 MPa or more, the shrinkage initiation temperature of the heat-shrinkable film can be sufficiently increased to suppress spontaneous shrinkage. When the tensile modulus is 4000 MPa or less, the low-temperature shrinkability and shrink finish of the heat-shrinkable film can be improved, and deterioration of the low-temperature shrinkability over time can be suppressed.
A more preferable lower limit of the tensile modulus is 1500 MPa, and a more preferable upper limit is 3700 MPa.
The tensile modulus can be measured by a method conforming to ASTM-D882 (TestA).

Examples of commercially available polyester resins constituting the front and back layers include "Easter", "EmbraceLv" (manufactured by Eastman Chemical Co.), "Belpet" (manufactured by Bell Polyester Products), "Novaduran" (Mitsubishi Engineering Plastics Co., Ltd.) and the like.

As the polyester-based resin contained in the front and back layers, a polyester-based resin having the composition described above may be used alone, or two or more polyester-based resins having the composition described above may be used in combination. Further, the polyester resin may be a polyester resin having a different composition between the surface layer and the back layer. is preferred.

The front and back layers contain organic fine particles.
As the organic fine particles, organic fine particles such as acrylic resin fine particles, styrene resin fine particles, styrene-acrylic resin fine particles, urethane resin fine particles, and silicone resin fine particles can be used. These may or may not be crosslinked, but are preferably crosslinked in order to increase the heat resistance of the fine particles. Among them, from the viewpoint of compatibility with the polyester resin, acrylic resin fine particles are preferable, and polymethyl methacrylate crosslinked fine particles are more preferable.

The front and back layers preferably contain at least two kinds of organic fine particles.
By using two or more kinds of organic fine particles in combination, it is possible to sufficiently exhibit the effect of improving anti-blocking properties and suppressing defective trapping.

The organic fine particles include organic fine particles (A) having an average particle size of 0.5 to 2.9 μm and organic fine particles (B) having an average particle size of 3.0 to 10.0 μm. is preferred.

The average particle size of the organic fine particles (A) has a more preferable lower limit of 1.8 μm and a more preferable upper limit of 2.4 μm.
The average particle size of the organic fine particles (B) has a more preferable lower limit of 3.2 μm and a more preferable upper limit of 3.8 μm.
The ratio of the average particle size of the organic fine particles (A) to the average particle size of the organic fine particles (B) (average particle size of the organic fine particles (A)/average particle size of the organic fine particles (B)) is , the preferred lower limit is 0.5/10.0, the more preferred lower limit is 1.8/10.0, the preferred upper limit is 2.9/3.0, and the more preferred upper limit is 2.4/3.0.
The average particle size can be measured by, for example, a laser diffraction/scattering method.

The content of the organic fine particles in the front and back layers has a lower limit of 0.055 parts by weight and an upper limit of 0.145 parts by weight with respect to 100 parts by weight of the polyester resin.
When the content of the organic fine particles is 0.055 parts by weight or more, antiblocking properties can be improved. When the content of the organic fine particles is 0.145 parts by weight or less, trapping defects can be prevented.
A preferred lower limit to the content of the organic fine particles is 0.06 parts by weight, and a preferred upper limit is 0.125 parts by weight.

The content of the organic fine particles (A) in the front and back layers preferably has a lower limit of 0.015 parts by weight, a more preferred lower limit of 0.02 parts by weight, and a preferred upper limit of 0.015 parts by weight, relative to 100 parts by weight of the polyester resin. 13 parts by weight, and a more preferable upper limit is 0.12 parts by weight.
The content of the organic fine particles (B) in the front and back layers preferably has a lower limit of 0.015 parts by weight, a more preferred lower limit of 0.02 parts by weight, and a preferred upper limit of 0.015 parts by weight, relative to 100 parts by weight of the polyester resin. 13 parts by weight, and a more preferable upper limit is 0.12 parts by weight.
The ratio of the content of the organic fine particles (A) to the content of the organic fine particles (B) in the front and back layers (content of organic fine particles (A)/content of organic fine particles (B)) is , the preferred lower limit is 0.015/0.13, the more preferred lower limit is 0.02/0.12, the preferred upper limit is 0.13/0.015, and the more preferred upper limit is 0.12/0.02.

The front and back layers may contain additives such as antioxidants, heat stabilizers, ultraviolet absorbers, light stabilizers, lubricants, antistatic agents, flame retardants, antibacterial agents, fluorescent whitening agents, and colorants, if necessary. may contain.

(middle layer)
The heat-shrinkable multilayer film of the present invention has the above intermediate layer.
The intermediate layer contains a polystyrene resin.
Examples of the polystyrene resin include aromatic vinyl hydrocarbon-conjugated diene copolymer, aromatic vinyl hydrocarbon-conjugated diene copolymer and aromatic vinyl hydrocarbon-unsaturated aliphatic carboxylic acid ester copolymer. and rubber-modified impact-resistant polystyrene. By using the above polystyrene-based resin, the heat-shrinkable multilayer film of the present invention can start shrinking at a low temperature and has high shrinkability.

As used herein, the aromatic vinyl hydrocarbon-conjugated diene copolymer refers to a copolymer containing a component derived from an aromatic vinyl hydrocarbon and a component derived from a conjugated diene.
The aromatic vinyl hydrocarbon is not particularly limited, and examples thereof include styrene, o-methylstyrene, p-methylstyrene and the like. These may be used alone or in combination of two or more. The conjugated diene is not particularly limited, and examples include 1,3-butadiene, 2-methyl-1,3-butadiene, 2,3-dimethyl-1,3-butadiene, 1,3-pentadiene, and 1,3-hexadiene. etc. These may be used alone or in combination of two or more.

The above aromatic vinyl hydrocarbon-conjugated diene copolymer preferably contains a styrene-butadiene copolymer (SBS resin) because it is particularly excellent in heat shrinkability. In order to produce a heat-shrinkable multi-layer film with less fish eyes, the aromatic vinyl hydrocarbon-conjugated diene copolymer contains 2-methyl-1,3-butadiene (isoprene) as the conjugated diene. It preferably contains the styrene-isoprene copolymer (SIS resin), styrene-isoprene-butadiene copolymer (SIBS), etc. used.
The above aromatic vinyl hydrocarbon-conjugated diene copolymer may contain any one of SBS resin, SIS resin and SIBS resin alone, or may contain a plurality of them in combination. In addition, when using a plurality of SBS resins, SIS resins and SIBS resins, each resin may be dry blended, and a compound resin obtained by kneading each resin with a specific composition using an extruder and pelletizing is used. may

When the aromatic vinyl hydrocarbon-conjugated diene copolymer contains the SBS resin, the SIS resin and the SIBS resin singly or in combination, a heat-shrinkable multilayer film having particularly excellent heat-shrinkability can be obtained. It is preferable that the aromatic vinyl hydrocarbon-conjugated diene copolymer has a styrene content of 65 to 90% by weight and a conjugated diene content of 10 to 35% by weight based on 100% by weight. If the styrene content is more than 90% by weight or the conjugated diene content is less than 10% by weight, the heat-shrinkable multilayer film may be easily cut when tension is applied, or may be difficult to handle during processing such as printing. It may break without twisting. If the styrene content is less than 65% by weight or the conjugated diene content is more than 35% by weight, foreign substances such as gels are likely to occur during molding, and the stiffness of the heat-shrinkable multilayer film becomes weak. and the handleability may deteriorate.

In the present specification, the aromatic vinyl hydrocarbon-unsaturated aliphatic carboxylic acid ester copolymer contains a component derived from the aromatic vinyl hydrocarbon and a component derived from the unsaturated aliphatic carboxylic acid ester. Copolymer.
The aromatic vinyl hydrocarbon is not particularly limited, and the same aromatic vinyl hydrocarbon as exemplified in the aromatic vinyl hydrocarbon-conjugated diene copolymer can be used. The aliphatic unsaturated carboxylic acid ester is not particularly limited, and examples thereof include methyl (meth) acrylate, butyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, lauryl (meth) acrylate, stearyl (meth) acrylate, and the like. be done. Here, (meth)acrylate indicates both acrylate and methacrylate.

When a styrene-butyl acrylate copolymer is used as the aromatic vinyl hydrocarbon-aliphatic unsaturated carboxylic acid ester copolymer, the styrene content in 100% by weight of the styrene-butyl acrylate copolymer is 60. -90% by weight, preferably with a butyl acrylate content of 10-40% by weight. By using the aromatic vinyl hydrocarbon-unsaturated aliphatic carboxylic acid ester copolymer having such a composition, a heat-shrinkable multilayer film having excellent heat-shrinkability can be obtained.

The mixed resin of the aromatic vinyl hydrocarbon-conjugated diene copolymer and the aromatic vinyl hydrocarbon-unsaturated aliphatic carboxylic acid ester copolymer is not particularly limited, but the aromatic vinyl hydrocarbon-aliphatic unsaturated carboxylic acid ester copolymer is not particularly limited. It is preferable to use a mixed resin in which the content of the saturated carboxylic acid ester copolymer is 80% by weight or less.

The rubber-modified high-impact polystyrene is composed of a continuous phase comprising a terpolymer of styrene, alkyl methacrylate, and alkyl acrylate, and a dispersed phase comprising a rubber component mainly composed of a conjugated diene. It is the basis.

Examples of the alkyl methacrylate forming the continuous phase include methyl methacrylate and ethyl methacrylate, and examples of the alkyl acrylate include methyl acrylate, ethyl acrylate, propyl acrylate and butyl acrylate.
The proportion of styrene in the copolymer forming the continuous phase is preferably 20 to 80% by weight, more preferably 30 to 70% by weight. The proportion of alkyl methacrylate is preferably 10 to 50% by weight, more preferably 15 to 40% by weight. The proportion of alkyl acrylate is preferably 1 to 30% by weight, more preferably 5 to 20% by weight.

Polybutadiene or a styrene-butadiene copolymer having a styrene content of 5 to 30% by weight is preferable as the rubber component mainly composed of a conjugated diene that forms the dispersed phase.
The particle size of the conjugated diene-based rubber component forming the dispersed phase is preferably 0.1 to 1.2 μm, more preferably 0.3 to 0.8 μm. If the particle size is less than 0.1 μm, the impact resistance of the rubber-modified high-impact polystyrene may be insufficient, and if it exceeds 1.2 μm, the transparency of the intermediate layer may decrease.

In the rubber-modified high-impact polystyrene, the proportion of the continuous phase composed of a terpolymer of styrene, alkyl methacrylate, and alkyl acrylate is 70 to 95% by weight, and the proportion of the dispersed phase composed of a rubber component mainly composed of a conjugated diene is A proportion of 5 to 20% by weight is preferred. If the proportion of the dispersed phase is less than 5% by weight, the impact resistance of the rubber-modified high-impact polystyrene may be insufficient, and if it exceeds 20% by weight, the transparency of the intermediate layer may be reduced. There is

The preferred lower limit of the Vicat softening temperature of the polystyrene resin is 50°C, and the preferred upper limit is 90°C. When the Vicat softening temperature is 50° C. or higher, the low-temperature shrinkability of the heat-shrinkable multilayer film can be improved, and wrinkles can be suppressed when the film is attached to a container. When the Vicat softening temperature is 90° C. or lower, the low-temperature shrinkability of the heat-shrinkable multilayer film can be sufficiently enhanced to prevent the occurrence of unshrunk portions when the film is attached to a container. A more preferable lower limit of the Vicat softening temperature is 55°C, and a more preferable upper limit is 85°C. The Vicat softening temperature can be measured by a method conforming to ISO 306.

A preferred lower limit of the MFR (melt flow rate) at 200° C. of the polystyrene resin is 2 g/10 minutes, and a preferred upper limit is 15 g/10 minutes.
When the MFR at 200° C. is 2 g/10 minutes or more, the film formability of the film can be improved. When the MFR at 200°C is 15 g/10 minutes or less, the mechanical strength of the film can be sufficiently improved.
A more preferred lower limit of MFR at 200° C. is 4 g/10 min, and a more preferred upper limit is 12 g/10 min. In addition, MFR can be measured by the method based on ISO1133.

Examples of commercially available polystyrene resins constituting the intermediate layer include "Clearen" (manufactured by Denki Kagaku Kogyo), "Asaflex" (manufactured by Asahi Kasei Chemicals), "Styrolux" (manufactured by BASF), and "PSJ." -Polystyrene” (manufactured by PS Japan Co., Ltd.).

The preferable lower limit of the content of the polystyrene-based resin in the intermediate layer is 80% by weight, and the preferable upper limit thereof is 100% by weight.
When the content of the polystyrene-based resin is at least the lower limit and at most the upper limit, excellent perforation cutting properties can be obtained in both the MD and TD directions.
The content of the polystyrene resin in the intermediate layer has a more preferable lower limit of 85% by weight, a more preferable upper limit of 99% by weight, and an even more preferable upper limit of 95% by weight.

The intermediate layer preferably contains 0 to 60% by weight of a polystyrene resin having a Vicat softening temperature of 80° C. or higher.
By containing a predetermined amount of the polystyrene-based resin having a Vicat softening temperature of 80° C. or higher, it is possible to further improve the effect of preventing loosening during dry heat shrinkage.
The content of the polystyrene resin having a Vicat softening temperature of 80° C. or higher in the intermediate layer has a more preferable lower limit of 10% by weight, a more preferable lower limit of 20% by weight, and a more preferable upper limit of 50% by weight.
The upper limit of the Vicat softening temperature of the polystyrene resin having a Vicat softening temperature of 80°C or higher is preferably 90°C, more preferably 85°C.

The intermediate layer preferably contains 40 to 100% by weight of a polystyrene resin having a Vicat softening temperature of less than 80.degree.
By containing a predetermined amount of the polystyrene-based resin having a Vicat softening temperature of less than 80° C., it is possible to further improve the effect of preventing loosening during dry heat shrinkage.
The content of the polystyrene resin having a Vicat softening temperature of less than 80° C. in the intermediate layer has a more preferable lower limit of 50% by weight, a more preferable upper limit of 90% by weight, and an even more preferable upper limit of 80% by weight.
The lower limit of the Vicat softening temperature of the polystyrene resin having a Vicat softening temperature of less than 80°C is preferably 50°C, more preferably 55°C.

The ratio of the content of the polystyrene-based resin having a Vicat softening temperature of 80° C. or higher and the content of the polystyrene-based resin having a Vicat softening temperature of lower than 80° C. in the intermediate layer (the Vicat softening temperature of 80° C. or higher The content of polystyrene-based resin/the content of polystyrene-based resin having a Vicat softening temperature of less than 80°C) has a preferred lower limit of 0/100, a more preferred lower limit of 10/90, a more preferred lower limit of 20/80, and a preferred upper limit of is 60/40, and a more preferred upper limit is 50/50.

The difference in Vicat softening temperature between the polystyrene resin having a Vicat softening temperature of 80° C. or higher and the polystyrene resin having a Vicat softening temperature of less than 80° C. is preferably 5° C. or higher, and is 10° C. or higher. is more preferably 25° C. or lower, and more preferably 20° C. or lower.

When the intermediate layer contains a mixed resin containing a polystyrene resin having a Vicat softening temperature of 80° C. or higher and a polystyrene resin having a Vicat softening temperature of less than 80° C., the apparent Vicat softening of the mixed resin is The preferred lower limit of the temperature is 65°C, the more preferred lower limit is 68°C, the preferred upper limit is 78°C, and the more preferred upper limit is 77°C.
The Vicat softening temperature can be measured by a method conforming to ISO 306.

The intermediate layer may further contain a polyester resin.
Examples of the polyester-based resin that can be used for the intermediate layer include those similar to those that can be used for the front and back layers.
As the polyester-based resin, the same one as that constituting the front and back layers may be used, or a different one may be used.

The preferred lower limit of the content of the polyester resin in the intermediate layer is 1% by weight, and the preferred upper limit is 20% by weight.
When the content of the polyester resin is equal to or more than the lower limit and equal to or less than the upper limit, excellent perforation cuttability can be obtained in both the MD direction and the TD direction.
A more preferable lower limit to the content of the polyester-based resin in the intermediate layer is 5% by weight, and a more preferable upper limit is 17% by weight.

The intermediate layer may further contain a polyester elastomer.
As the polyester-based elastomer, the same ones as those that can be used for the adhesive layer described later can be used.

The content of the polyester elastomer in the intermediate layer preferably has a lower limit of 0% by weight, a more preferred lower limit of 0.1% by weight, a preferred upper limit of 1.0% by weight, and a more preferred upper limit of 0.7% by weight. .

The intermediate layer may further contain a styrene-based elastomer.
As the styrene-based elastomer, the same ones that can be used for the adhesive layer described later can be used.

The preferred lower limit of the content of the styrene-based elastomer in the intermediate layer is 0% by weight, the more preferred lower limit is 2% by weight, the preferred upper limit is 10% by weight, and the more preferred upper limit is 7% by weight.

Additives such as antioxidants, heat stabilizers, ultraviolet absorbers, light stabilizers, lubricants, antistatic agents, flame retardants, antibacterial agents, fluorescent whitening agents, and colorants may be added to the intermediate layer as necessary. may contain.

(adhesive layer)
When higher interlayer adhesive strength is required between the front and back layers and the intermediate layer, the heat-shrinkable multilayer film of the present invention is obtained by laminating the front and back layers and the intermediate layer with an adhesive layer interposed therebetween. It is preferable to be
By having an adhesive layer, the adhesive strength between each layer of the heat-shrinkable multilayer film can be increased.

The adhesive layer preferably contains a polystyrene-based resin, a polyester-based resin, a styrene-based elastomer, or a polyester-based elastomer.

The polystyrene-based resin constituting the adhesive layer preferably contains an aromatic vinyl hydrocarbon-conjugated diene copolymer, particularly a styrene-butadiene copolymer (SBS resin), because of its excellent adhesiveness. It is preferable to contain In addition, in order to produce a heat-shrinkable multilayer film with more excellent adhesion, 2-methyl-1,3-butadiene (isoprene) was used as the conjugated diene of the aromatic vinyl hydrocarbon-conjugated diene copolymer. It preferably contains a styrene-isoprene copolymer (SIS resin), a styrene-isoprene-butadiene copolymer (SIBS resin), or the like.
As the polystyrene-based resin, any one of SBS resin, SIS resin, and SIBS resin may be used alone, or a plurality thereof may be used in combination. Further, when a plurality of SBS resins, SIS resins and SIBS resins are used in combination, each resin may be dry blended, and a compound resin obtained by kneading each resin with a specific composition using an extruder and pelletizing is used. may

The preferred lower limit of the styrene component content in the polystyrene resin constituting the adhesive layer is 50% by weight, the more preferred lower limit is 60% by weight, the preferred upper limit is 90% by weight, and the more preferred upper limit is 85% by weight.

The preferable lower limit of the content of the conjugated diene component in the polystyrene resin constituting the adhesive layer is 10% by weight, the more preferable lower limit is 15% by weight, the preferable upper limit is 50% by weight, and the more preferable upper limit is 40% by weight.

The preferred lower limit of the Vicat softening temperature of the polystyrene-based resin constituting the adhesive layer is 55°C, and the preferred upper limit is 85°C.
When the Vicat softening temperature is 55° C. or higher, it is possible to prevent peeling between layers due to heating when a heat-shrinkable label having a heat-shrinkable multilayer film as a base film is attached to a container. When the Vicat softening temperature is 85° C. or lower, the interlayer adhesive strength of the heat-shrinkable multilayer film can be sufficiently improved.
The Vicat softening temperature preferably has a lower limit of 60°C, a more preferred lower limit of 65°C, and a more preferred upper limit of 80°C.
The Vicat softening temperature can be measured by a method conforming to ISO 306.

The preferred lower limit of the MFR (melt flow rate) at 200° C. of the polystyrene resin constituting the adhesive layer is 2 g/10 minutes, and the preferred upper limit is 15 g/10 minutes.
When the MFR at 200° C. is 2 g/10 minutes or more, the resin is less likely to stagnate in the extruder, and the generation of foreign matter such as gel can be prevented. When the MFR at 200° C. is 15 g/10 minutes or less, the pressure in the film-forming process can be made uniform and the thickness can be made uniform.
The MFR has a more preferable lower limit of 4 g/10 minutes and a more preferable upper limit of 12 g/10 minutes.
In addition, MFR can be measured by the method based on ISO1133.

As the polystyrene-based resin, the same one as that constituting the intermediate layer may be used, or a different one may be used.

The preferable lower limit of the content of the polystyrene resin in the adhesive layer is 10% by weight, the more preferable lower limit is 20% by weight, the preferable upper limit is 95% by weight, and the more preferable upper limit is 80% by weight.

As the polyester-based resin constituting the adhesive layer, a resin obtained by condensation polymerization of a dicarboxylic acid and a diol can be used.
The dicarboxylic acid is not particularly limited, and examples thereof include o-phthalic acid, terephthalic acid, isophthalic acid, succinic acid, adipic acid, sebacic acid, azelaic acid, octylsuccinic acid, cyclohexanedicarboxylic acid, naphthalenedicarboxylic acid, fumaric acid, Maleic acid, itaconic acid, decamethylenecarboxylic acid, their anhydrides and lower alkyl esters.
The diol is not particularly limited, and examples include ethylene glycol, 1,3-propanediol, 1,4-butanediol, diethylene glycol, 1,5-pentanediol, 1,6-hexanediol, dipropylene glycol, and triethylene. Glycol, tetraethylene glycol, 1,2-propanediol, 1,3-butanediol, 2,3-butanediol, neopentyl glycol (2,2-dimethylpropane-1,3-diol), 1,2-hexane aliphatic diols such as diols, 2,5-hexanediol, 2-methyl-2,4-pentanediol, 3-methyl-1,3-pentanediol and 2-ethyl-1,3-hexanediol;2, Alicyclic diols such as 2-bis(4-hydroxycyclohexyl)propane, alkylene oxide adducts of 2,2-bis(4-hydroxycyclohexyl)propane, 1,4-cyclohexanediol, and 1,4-cyclohexanedimethanol etc.

As the polyester-based resin, among others, those containing a component derived from terephthalic acid as a dicarboxylic acid component and containing a component derived from ethylene glycol and 1,4-cyclohexanedimethanol as a diol component are preferable. can be used.
Moreover, as the polyester-based resin, those containing a component derived from terephthalic acid as a dicarboxylic acid component and a component derived from 1,4-butanediol as a diol component can also be suitably used.

The preferred lower limit of the glass transition temperature of the polyester-based resin is 30°C, the more preferred lower limit is 55°C, the preferred upper limit is 95°C, and the more preferred upper limit is 90°C.
The glass transition temperature can be measured with a differential scanning calorimeter (DSC).

The preferred lower limit of the tensile modulus of the polyester-based resin is 1000 MPa, the more preferred lower limit is 1500 MPa, the preferred upper limit is 4000 MPa, and the more preferred upper limit is 3700 MPa.
The tensile modulus can be measured by a method conforming to ASTM-D992 (TestA).

As the polyester-based resin, the same one as that constituting the front and back layers may be used, or a different one may be used.

Examples of the styrene-based elastomer constituting the adhesive layer include resins composed of polystyrene as a hard segment and polybutadiene, polyisoprene, or a copolymer of polybutadiene and polyisoprene as a soft segment, and hydrogenated products thereof. etc. The hydrogenated material may be partially hydrogenated polybutadiene, polyisoprene, or the like, or may be entirely hydrogenated.

The styrene-based elastomer may be a modified product.
Examples of modified styrene elastomers include those modified with functional groups such as carboxylic acid groups, acid anhydride groups, amino groups, epoxy groups and hydroxyl groups.

The preferable lower limit of the functional group content in the modified styrene elastomer is 0.05% by weight, and the preferable upper limit is 5.0% by weight.
When the content of the functional group is 0.05% by weight or more, the interlaminar strength of the heat-shrinkable multilayer film can be sufficiently increased. When the content of the functional group is 5.0% by weight or less, it is possible to suppress the generation of gel or the like due to thermal deterioration of the styrene elastomer.
A more preferable lower limit to the content of the functional group is 0.1% by weight, and a more preferable upper limit is 3.0% by weight.

Commercially available products of the styrene-based elastomer or modified styrene-based elastomer include, for example, Tuftec, Tufprene (both of which are manufactured by Asahi Kasei Chemicals), Kraton (manufactured by Kraton Polymer Japan), Dynalon, JSR TR, JSR SIS (manufactured by JSR), Septon (manufactured by Kuraray), and the like.

The polyester-based elastomer is composed of polyester as a hard segment and polyether or polyester as a soft segment having high rubber elasticity. Specifically, for example, aromatic polyester as a hard segment and , a block copolymer composed of an aliphatic polyether or an aliphatic polyester as a soft segment, and the like, preferably a saturated polyester elastomer, particularly a saturated polyalkylene ether glycol segment containing a polyalkylene ether glycol segment as a soft segment. A polyester-based elastomer is preferred.
As the saturated polyester elastomer containing the polyalkylene ether glycol segment, for example, a block copolymer composed of an aromatic polyester as a hard segment and a polyalkylene ether glycol as a soft segment is preferable.

When a block copolymer composed of an aromatic polyester and a polyalkylene ether glycol is used as the polyester-based elastomer, the proportion of the segment composed of the polyalkylene ether glycol preferably has a lower limit of 5% by weight and an upper limit of 90% by weight. be.
When the proportion of the segment composed of the polyalkylene ether glycol is 5% by weight or more, the adhesion to the intermediate layer can be sufficiently improved, and when it is 90% by weight or less, the adhesion to the front and back layers is sufficiently improved. can be enhanced.
The more preferable lower limit of the proportion of the segment composed of the polyalkylene ether glycol is 30% by weight, the more preferable lower limit is 55% by weight, and the more preferable upper limit is 80% by weight.

Examples of the polyalkylene ether glycol include polyethylene glycol, poly(propylene ether) glycol, poly(tetramethylene ether) glycol, poly(hexanemethylene ether) glycol and the like.

The number average molecular weight of the polyalkylene ether glycol has a preferred lower limit of 400, a more preferred lower limit of 600, a still more preferred lower limit of 1000, a preferred upper limit of 6000, a more preferred upper limit of 4000, and an even more preferred upper limit of 3000.
When the number average molecular weight is within the above preferable range, the interlaminar strength can be further improved.
The number average molecular weight can be measured by gel permeation chromatography (GPC).

The method for producing the polyester-based elastomer is not particularly limited, but for example, (i) an aliphatic and/or alicyclic diol having 2 to 12 carbon atoms, Using dicarboxylic acids or their esters and (iii) a polyalkylene ether glycol having a number average molecular weight of 400 to 6000 as raw materials, obtaining an oligomer by an esterification reaction or a transesterification reaction, and then polycondensing the oligomer. It can be produced by

Examples of the aliphatic and/or alicyclic diols having 2 to 12 carbon atoms include those commonly used as raw materials for polyesters, particularly polyester thermoplastic elastomers. Specific examples include ethylene glycol, propylene glycol, trimethylene glycol, 1,4-butanediol, 1,4-cyclohexanediol, 1,4-cyclohexanedimethanol and the like. Among them, ethylene glycol and 1,4-butanediol are preferred, and 1,4-butanediol is more preferred.
These may be used alone or in combination of two or more.

Examples of the aromatic dicarboxylic acid and/or alicyclic dicarboxylic acid include those commonly used as raw materials for polyesters, particularly polyester thermoplastic elastomers. Specific examples include terephthalic acid, isophthalic acid, phthalic acid, 2,6-naphthalenedicarboxylic acid, cyclohexanedicarboxylic acid and the like. Among them, terephthalic acid and 2,6-naphthalenedicarboxylic acid are preferred, and terephthalic acid is more preferred.
These may be used alone or in combination of two or more.

Examples of commercially available polyester-based elastomers include "Primalloy" (manufactured by Mitsubishi Chemical Corporation), "Pelprene" (manufactured by Toyobo Co., Ltd.), and "Hytrel" (manufactured by Toray DuPont).

The preferred lower limit of the melting point of the polyester-based elastomer is 120°C, and the preferred upper limit is 200°C.
When the melting point is 120° C. or higher, the heat resistance can be sufficiently enhanced, and peeling from the solvent-sealed portion can be prevented when the label is coated on a container as a heat-shrinkable label. When the melting point is 200° C. or lower, the adhesive strength can be sufficiently increased.
A more preferable lower limit of the melting point is 130°C, and a more preferable upper limit is 190°C.
The melting point can be measured using a differential scanning calorimeter (DSC-60, manufactured by Shimadzu Corporation) or the like under the condition of a heating rate of 10° C./min.

The melting point of the polyester-based elastomer is caused by the copolymerization ratio and structure of the hard segment polyester and the soft segment polyether or polyester.
In general, the melting point of a polyester-based elastomer tends to depend on the copolymerization amount of polyether or polyester, which is the soft segment.
Further, the melting point of the polyester, which is a hard segment constituting the polyester-based elastomer, can be adjusted by changing the copolymer component to adjust the melting point of the entire polyester-based elastomer.
Furthermore, when the molecular weight of the polyether or polyester, which is the soft segment, becomes small, the blocking property of the obtained polyester-based elastomer is lowered, so that the melting point tends to be lowered.

The durometer hardness of the polyester-based elastomer has a preferable lower limit of 10 and a preferable upper limit of 80.
When the durometer hardness is 10 or more, the mechanical strength of the adhesive layer can be improved. When the durometer hardness is 80 or less, the flexibility and impact resistance of the adhesive layer can be improved.
The durometer hardness has a more preferable lower limit of 15, a more preferable lower limit of 20, a more preferable upper limit of 70, and a further preferable upper limit of 60.
The durometer hardness can be measured by using a durometer type D in accordance with ISO18517.

The specific gravity of the polyester elastomer has a preferred lower limit of 0.95 and a preferred upper limit of 1.20.
When the specific gravity is 0.95 or more, the heat resistance can be sufficiently improved, and peeling from the solvent-sealed portion can be prevented when the label is coated on a container as a heat-shrinkable label. Adhesion strength can fully be raised as the said specific gravity is 1.20 or less.
A more preferable lower limit to the specific gravity is 0.98, and a more preferable upper limit is 1.18.
The above specific gravity can be measured using a water substitution method in accordance with ISO 1183.

The adhesive layer may contain polystyrene-based resin, polyester-based resin, styrene-based elastomer, or polyester-based elastomer singly, or may contain two or more of these.

When the adhesive layer contains a mixed resin of the polystyrene resin and the polyester elastomer, the content of the polystyrene resin in the adhesive layer preferably has a lower limit of 20% by weight, and a more preferred lower limit of 25% by weight. , the preferred upper limit is 80% by weight, and the more preferred upper limit is 75% by weight.
The preferable lower limit of the content of the polyester-based elastomer in the adhesive layer is 20% by weight, the more preferable lower limit is 25% by weight, the preferable upper limit is 80% by weight, and the more preferable upper limit is 75% by weight.

When the adhesive layer contains a mixed resin of the polystyrene-based resin and the polyester-based resin, the content of the polystyrene-based resin in the adhesive layer has a preferable lower limit of 20% by weight, and a more preferable lower limit of 25% by weight. , the preferred upper limit is 80% by weight, and the more preferred upper limit is 75% by weight.
The preferable lower limit of the content of the polyester-based resin in the adhesive layer is 20% by weight, the more preferable lower limit is 25% by weight, the preferable upper limit is 80% by weight, and the more preferable upper limit is 75% by weight.

When the adhesive layer contains a mixed resin of the polyester resin and the styrene elastomer, the content of the polyester resin in the adhesive layer preferably has a lower limit of 20% by weight, and a more preferred lower limit of 25% by weight. , the preferred upper limit is 80% by weight, and the more preferred upper limit is 75% by weight.
The preferred lower limit of the content of the styrene-based elastomer in the adhesive layer is 20% by weight, the more preferred lower limit is 25% by weight, the preferred upper limit is 80% by weight, and the more preferred upper limit is 75% by weight.

When the adhesive layer contains the polystyrene-based resin, the polyester-based resin, and the mixed resin containing the styrene-based elastomer or the polyester-based elastomer, the content of the polystyrene-based resin in the adhesive layer is a preferable lower limit. is 10% by weight, a more preferred lower limit is 20% by weight, a preferred upper limit is 80% by weight, and a more preferred upper limit is 75% by weight.
The preferable lower limit of the content of the polyester-based resin in the adhesive layer is 10% by weight, the more preferable lower limit is 20% by weight, the preferable upper limit is 80% by weight, and the more preferable upper limit is 75% by weight.
The content of the styrene-based elastomer or polyester-based elastomer in the adhesive layer preferably has a lower limit of 2% by weight, a more preferred lower limit of 4% by weight, a preferred upper limit of 10% by weight, and a more preferred upper limit of 8% by weight.

Antioxidants, heat stabilizers, lubricants, antistatic agents, and the like may be added to the adhesive layer as necessary.

The thickness of the entire heat-shrinkable multilayer film of the present invention has a preferred lower limit of 20 µm, a preferred upper limit of 80 µm, a more preferred lower limit of 25 µm, and a more preferred upper limit of 70 µm. When the thickness of the entire heat-shrinkable multilayer film is within the above range, excellent heat-shrinkability, excellent converting properties such as printing or center sealing, and excellent wearability can be obtained.
In the heat-shrinkable multilayer film of the present invention, the thickness of the intermediate layer has a preferable lower limit of 50% and a preferable upper limit of 90% of the thickness of the entire heat-shrinkable multilayer film. When the thickness of the intermediate layer is within the above range, high interlayer strength, high transparency, and the like can be obtained.

The coefficient of dynamic friction of the heat-shrinkable multilayer film of the present invention has a preferred lower limit of 0.1, a preferred upper limit of 0.55, a more preferred lower limit of 0.15, and a more preferred upper limit of 0.52. By setting the dynamic friction coefficient within the above range, problems such as blocking can be prevented. Moreover, the handleability of the obtained heat-shrinkable multilayer film can be improved.

The preferable lower limit of the heat shrinkage rate in the main shrinkage direction (TD direction) when the heat-shrinkable multilayer film of the present invention is immersed in hot water at 70° C. for 10 seconds is 10%. When the heat shrinkage rate is 10% or more, problems such as shrinkage defects such as wrinkles and distortion do not occur, and the film can be suitably used as a heat-shrinkable multilayer film.
A more preferable lower limit of the heat shrinkage rate is 20%, and a preferable upper limit thereof is 50%.
The preferred lower limit of the heat shrinkage rate in the main shrinkage direction (TD direction) when the heat-shrinkable multilayer film of the present invention is immersed in hot water at 100° C. for 10 seconds is 60%. When the heat shrinkage rate is 60% or more, problems such as shrinkage defects such as wrinkles and distortion do not occur, and the film can be suitably used as a heat-shrinkable multilayer film.
A more preferable lower limit of the heat shrinkage rate is 62%, and a preferable upper limit thereof is 85%.

The preferable lower limit of the tensile elongation at break of the heat-shrinkable multilayer film of the present invention in a direction perpendicular to the main shrinkage direction (MD direction) in a 5° C. atmosphere is 100%.
When the tensile elongation at break is 100% or more, the film is less likely to break in steps such as printing and sealing, and productivity is improved.
A more preferable lower limit of the tensile elongation at break is 200%, and a preferable upper limit thereof is 400%.

The natural shrinkage rate in the main shrinkage direction (TD direction) when the heat-shrinkable multilayer film of the present invention is left in an atmosphere of 40° C. for 7 days is preferably less than 3.0%.
When the natural shrinkage rate is less than 3.0%, the shrinkage during storage is small and problems such as poor shrinkage do not occur, and the film can be suitably used as a heat-shrinkable multilayer film.
More preferably, the natural shrinkage rate is less than 2.8%.

The preferable lower limit of the delamination strength of the heat-shrinkable multilayer film of the present invention is 0.4 N/10 mm.
When the delamination strength is 0.4 N/10 mm or more, peeling between the front and back layers and the intermediate layer is less likely to occur during printing/sealing and label mounting, and the label can be suitably used as a heat-shrinkable label.

The method for producing the heat-shrinkable multilayer film of the present invention is not particularly limited, but a method of forming each layer simultaneously by coextrusion is preferred. When the co-extrusion method is co-extrusion using a T-die, the lamination method may be a feed block method, a multi-manifold method, or a combination of these methods.

Specifically, the method for producing the heat-shrinkable multilayer film of the present invention includes, for example, extruding a raw material for forming the front and back layers, a raw material for forming the intermediate layer, and a raw material for forming the adhesive layer. It is put into a machine, extruded into a sheet with a die, cooled and solidified with a take-up roll, and then uniaxially or biaxially stretched.
As the stretching method, for example, a roll stretching method, a tenter stretching method, or a combination thereof can be used. The stretching temperature varies depending on the softening temperature of the resin constituting the film, the shrinkage properties required for the heat-shrinkable multilayer film, and the like. , and a more preferred upper limit is 115°C. The draw ratio in the main shrinkage direction varies depending on the resin constituting the film, the drawing means, the drawing temperature, etc., but is preferably 3 times or more, more preferably 4 times or more, and preferably 7 times or less. It is preferably 6 times or less. By setting the stretching temperature and the stretching ratio as such, excellent thickness accuracy can be achieved.

Although the use of the heat-shrinkable multilayer film of the present invention is not particularly limited, the heat-shrinkable multilayer film of the present invention is excellent in anti-blocking properties and can prevent trapping defects, so it can be used for containers such as PET bottles and metal cans. It is suitably used as a base film for a heat-shrinkable label to be attached to.

According to the present invention, it is possible to suppress the deterioration of feeding performance due to adhesion between films and the adhesion of labels after label attachment, reduce ink skipping during overprinting, and prevent trapping defects. A heat-shrinkable film can be provided.

EXAMPLES The aspects of the present invention will be described in more detail with reference to Examples below, but the present invention is not limited only to these Examples.

The following raw materials were used in Examples and Comparative Examples.
(polyester resin)
Polyester-based resin A: 100 mol% of a component derived from terephthalic acid as a dicarboxylic acid component, 65 mol% of a component derived from ethylene glycol as a diol component, 20 mol% of a component derived from diethylene glycol, 1,4-cyclohexane Polyester-based resin containing 15 mol% of a component derived from dimethanol (glass transition temperature 69°C)
Polyester-based resin B: 100 mol% of a component derived from terephthalic acid as a dicarboxylic acid component, 68 mol% of a component derived from ethylene glycol as a diol component, and 32 mol% of a component derived from 1,4-cyclohexanedimethanol. Containing polyester resin (glass transition temperature 82 ° C.)
(polystyrene resin)
- Polystyrene resin A: styrene-butadiene copolymer (styrene 78% by weight, butadiene 22% by weight, Vicat softening temperature 71°C)
- Polystyrene resin B: styrene-butadiene copolymer (80% by weight of styrene, 20% by weight of butadiene, Vicat softening temperature of 77°C)
- Polystyrene resin C: styrene-butadiene copolymer (82% by weight of styrene, 18% by weight of butadiene, Vicat softening temperature of 75°C)
- Polystyrene resin D: styrene-butadiene copolymer (81% by weight of styrene, 19% by weight of butadiene, Vicat softening temperature of 81°C)
- Polystyrene resin E: styrene-butadiene copolymer (styrene 71% by weight, butadiene 29% by weight, Vicat softening temperature 76°C)
(polyester elastomer)
Elastomer A: block copolymer composed of polybutylene terephthalate and polyether (melting point: 193°C, glass transition temperature: 45°C)
(polystyrene elastomer)
Elastomer B: modified styrene-butadiene copolymer hydrogenated product (acid value 2 mg CH ₃ ONa/g, styrene 30% by weight, MFR: 4.5 g/10 minutes)
(Organic fine particles)
Fine particles A: polymethyl methacrylate (PMMA) (average particle size: 2.2 μm, thermal decomposition initiation temperature: 270° C.)
Fine particles B: polymethyl methacrylate (PMMA) (average particle size: 3.3 μm, thermal decomposition initiation temperature: 270° C.)
(Inorganic fine particles)
Fine particles C: porous silica (average particle size: 4.0 μm)

(Example 1)
100% by weight of polyester-based resin A was used as the resin constituting the front and back layers, and fine particles A and fine particles B were added and mixed so that the content of fine particles A and fine particles B with respect to 100 parts by weight of polyester-based resin A would be the ratio shown in Table 1.
A mixed resin composed of 60% by weight of elastomer A and 40% by weight of polystyrene resin E was used as the resin constituting the adhesive layer.
As the resin constituting the intermediate layer, a mixed resin composed of 70% by weight of polystyrene resin C and 30% by weight of polystyrene resin D was used.
The raw materials for the front and back layers, the adhesive layer and the intermediate layer are put into an extruder with a barrel temperature of 160 to 250°C, extruded into a three-layer structure sheet from a multi-layer die at 250°C, and cooled and solidified with a take-up roll at 30°C. did. Next, roll stretching is performed in the MD direction at a stretching ratio of 1.5 times, followed by a preheating zone of 112°C (passing time of 5.3 seconds), a stretching zone of 100°C (passing time of 7.8 seconds), a heat setting zone of 102°C (passing time After stretching in the TD direction at a stretching ratio of 6 times in a tenter stretching machine with a time of 5.3 seconds), the total thickness is 40 μm by winding with a winding machine, and the surface layer (5.7 μm) / adhesive layer ( 0.7 μm)/intermediate layer (27.2 μm)/adhesive layer (0.7 μm)/backing layer (5.7 μm).

(Example 2)
100% by weight of polyester-based resin A was used as the resin constituting the front and back layers, and fine particles A and fine particles B were added and mixed so that the content of fine particles A and fine particles B with respect to 100 parts by weight of polyester-based resin A would be the ratio shown in Table 1.
A mixed resin composed of 40% by weight of elastomer A and 60% by weight of polystyrene resin E was used as the resin constituting the adhesive layer.
As the resin constituting the intermediate layer, a mixed resin composed of 70% by weight of polystyrene resin A and 30% by weight of polystyrene resin D was used.
A heat-shrinkable multilayer film was obtained in the same manner as in Example 1, except that these raw materials were used.
The obtained heat-shrinkable multilayer film had a total thickness of 40 μm, and was composed of surface layer (5.7 μm)/adhesive layer (0.7 μm)/intermediate layer (27.2 μm)/adhesive layer (0.7 μm)/back layer. (5.7 μm) and had a five-layer structure.

(Example 3)
100% by weight of polyester-based resin A was used as the resin constituting the front and back layers, and fine particles A and fine particles B were added and mixed so that the content of fine particles A and fine particles B with respect to 100 parts by weight of polyester-based resin A would be the ratio shown in Table 1.
As the resin constituting the adhesive layer, a mixed resin composed of 30% by weight of polyester resin A and 70% by weight of polystyrene resin E was used.
As the resin constituting the intermediate layer, 100% by weight of polystyrene resin B was used.
A heat-shrinkable multilayer film was obtained in the same manner as in Example 1, except that these raw materials were used.
The obtained heat-shrinkable multilayer film had a total thickness of 40 μm, and was composed of surface layer (5.7 μm)/adhesive layer (0.7 μm)/intermediate layer (27.2 μm)/adhesive layer (0.7 μm)/back layer. (5.7 μm) and had a five-layer structure.

(Example 4)
100% by weight of polyester resin B was used as the resin constituting the front and back layers, and fine particles A and fine particles B were added and mixed so that the content of fine particles A and fine particles B with respect to 100 parts by weight of polyester resin B was as shown in Table 1.
Elastomer A 100% by weight was used as the resin constituting the adhesive layer.
As the resin constituting the intermediate layer, 100% by weight of polystyrene resin A was used.
A heat-shrinkable multilayer film was obtained in the same manner as in Example 1, except that these raw materials were used.
The obtained heat-shrinkable multilayer film had a total thickness of 40 μm, and was composed of surface layer (5.7 μm)/adhesive layer (0.7 μm)/intermediate layer (27.2 μm)/adhesive layer (0.7 μm)/back layer. (5.7 μm) and had a five-layer structure.

(Example 5)
100% by weight of polyester resin B was used as the resin constituting the front and back layers, and fine particles A and fine particles B were added and mixed so that the content of fine particles A and fine particles B with respect to 100 parts by weight of polyester resin B was as shown in Table 1.
Elastomer B 100% by weight was used as the resin constituting the adhesive layer.
As the resin constituting the intermediate layer, 100% by weight of polystyrene resin A was used.
A heat-shrinkable multilayer film was obtained in the same manner as in Example 1, except that these raw materials were used.
The obtained heat-shrinkable multilayer film had a total thickness of 40 μm, and was composed of surface layer (5.7 μm)/adhesive layer (0.7 μm)/intermediate layer (27.2 μm)/adhesive layer (0.7 μm)/back layer. (5.7 μm) and had a five-layer structure.

(Comparative example 1)
100% by weight of polyester resin B was used as the resin constituting the front and back layers, and fine particles A and fine particles B were added and mixed so that the content of fine particles A and fine particles B with respect to 100 parts by weight of polyester resin B was as shown in Table 1.
Elastomer A 100% by weight was used as the resin constituting the adhesive layer.
As the resin constituting the intermediate layer, 100% by weight of polystyrene resin A was used.
A heat-shrinkable multilayer film was obtained in the same manner as in Example 1, except that these raw materials were used.
The obtained heat-shrinkable multilayer film had a total thickness of 40 μm, and was composed of surface layer (5.7 μm)/adhesive layer (0.7 μm)/intermediate layer (27.2 μm)/adhesive layer (0.7 μm)/back layer. (5.7 μm) and had a five-layer structure.

(Comparative example 2)
100% by weight of polyester-based resin A was used as the resin constituting the front and back layers, and fine particles A and fine particles B were added and mixed so that the content of fine particles A and fine particles B with respect to 100 parts by weight of polyester-based resin A would be the ratio shown in Table 1.
Elastomer A 100% by weight was used as the resin constituting the adhesive layer.
As the resin constituting the intermediate layer, 100% by weight of polystyrene resin A was used.
A heat-shrinkable multilayer film was obtained in the same manner as in Example 1, except that these raw materials were used.
The obtained heat-shrinkable multilayer film had a total thickness of 40 μm, and was composed of surface layer (5.7 μm)/adhesive layer (0.7 μm)/intermediate layer (27.2 μm)/adhesive layer (0.7 μm)/back layer. (5.7 μm) and had a five-layer structure.

(Comparative Example 3)
100% by weight of polyester-based resin A was used as the resin constituting the front and back layers, and fine particles A and fine particles B were added and mixed so that the content of fine particles A and fine particles B with respect to 100 parts by weight of polyester-based resin A would be the ratio shown in Table 1.
A mixed resin composed of 60% by weight of elastomer A and 40% by weight of polystyrene resin E was used as the resin constituting the adhesive layer.
As the resin constituting the intermediate layer, a mixed resin composed of 70% by weight of polystyrene resin C and 30% by weight of polystyrene resin D was used.
A heat-shrinkable multilayer film was obtained in the same manner as in Example 1, except that these raw materials were used.
The obtained heat-shrinkable multilayer film had a total thickness of 40 μm, and was composed of surface layer (5.7 μm)/adhesive layer (0.7 μm)/intermediate layer (27.2 μm)/adhesive layer (0.7 μm)/back layer. (5.7 μm) and had a five-layer structure.

(Comparative Example 4)
100% by weight of polyester resin A was used as the resin constituting the front and back layers, and fine particles A and fine particles B were added and mixed so that the content of fine particles A and fine particles B with respect to 100 parts by weight of polyester resin would be the ratio shown in Table 1.
A mixed resin composed of 60% by weight of elastomer A and 40% by weight of polystyrene resin E was used as the resin constituting the adhesive layer.
As the resin constituting the intermediate layer, a mixed resin composed of 70% by weight of polystyrene resin C and 30% by weight of polystyrene resin D was used.
A heat-shrinkable multilayer film was obtained in the same manner as in Example 1, except that these raw materials were used.
The obtained heat-shrinkable multilayer film had a total thickness of 40 μm, and was composed of surface layer (5.7 μm)/adhesive layer (0.7 μm)/intermediate layer (27.2 μm)/adhesive layer (0.7 μm)/back layer. (5.7 μm) and had a five-layer structure.

(Comparative Example 5)
100% by weight of polyester-based resin A was used as the resin constituting the front and back layers, and fine particles A and fine particles B were added and mixed so that the content of fine particles A and fine particles B with respect to 100 parts by weight of polyester-based resin A would be the ratio shown in Table 1.
Elastomer B 100% by weight was used as the resin constituting the adhesive layer.
As the resin constituting the intermediate layer, 100% by weight of polystyrene resin A was used.
A heat-shrinkable multilayer film was obtained in the same manner as in Example 1, except that these raw materials were used.
The obtained heat-shrinkable multilayer film had a total thickness of 40 μm, and was composed of surface layer (5.7 μm)/adhesive layer (0.7 μm)/intermediate layer (27.2 μm)/adhesive layer (0.7 μm)/back layer. (5.7 μm) and had a five-layer structure.

(Comparative Example 6)
100% by weight of polyester-based resin A was used as the resin constituting the front and back layers, and fine particles C were added and mixed so that the content of fine particles C with respect to 100 parts by weight of polyester-based resin would be the ratio shown in Table 1.
Elastomer B 100% by weight was used as the resin constituting the adhesive layer.
As the resin constituting the intermediate layer, 100% by weight of polystyrene resin A was used.
A heat-shrinkable multilayer film was obtained in the same manner as in Example 1, except that these raw materials were used.
The obtained heat-shrinkable multilayer film had a total thickness of 40 μm, and was composed of surface layer (5.7 μm)/adhesive layer (0.7 μm)/intermediate layer (27.2 μm)/adhesive layer (0.7 μm)/back layer. (5.7 μm) and had a five-layer structure.

(Comparative Example 7)
100% by weight of polyester resin A was used as the resin constituting the front and back layers. As the lubricant, oleic acid bisamide was used.
Elastomer B 100% by weight was used as the resin constituting the adhesive layer.
As the resin constituting the intermediate layer, 100% by weight of polystyrene resin A was used.
A heat-shrinkable multilayer film was obtained in the same manner as in Example 1, except that these raw materials were used.
The obtained heat-shrinkable multilayer film had a total thickness of 40 μm, and was composed of surface layer (5.7 μm)/adhesive layer (0.7 μm)/intermediate layer (27.2 μm)/adhesive layer (0.7 μm)/back layer. (5.7 μm) and had a five-layer structure.

(evaluation)
The heat-shrinkable multilayer films obtained in Examples and Comparative Examples were evaluated as follows. Table 1 shows the results.

(1) Blocking The heat-shrinkable multilayer films obtained in Examples and Comparative Examples were cut into 30 mm×40 mm pieces to prepare two samples. The obtained samples were superimposed and allowed to stand under conditions of a load of 5 kg/100 cm ² and 40° C. for 48 hours. Then, it was pulled in the shear direction at a tensile speed of 200 m/min, and the shear peel hardness was measured and evaluated according to the following criteria.
O: Shear peel strength was 2000 g/cm or less.
x: Shear peel strength exceeded 2000 g/cm.

(2) Trapping The obtained heat-shrinkable multilayer film was printed using a 5-color gravure printer under the following conditions.
Film width: 900mm
Printing ink: OSM type by Dainichiseika Kogyo Co., Ltd. Black, red, yellow, blue, white (base part)
Ink viscosity: Zahn cup method #3 Zahn cup for 15 seconds; Color chart plate made by engraving plate making Printing speed: 150 m/min
The state after printing was visually observed and evaluated according to the following criteria.
○: In the 5 to 20% portion of the 0 to 100% gradation curve, the outline can be printed clearly by visual observation or observation with a magnifying glass or a print defect detection device, or color loss (ink skipping) is less than 25 places. Met.
Δ: There were 25 to 50 areas of color loss (ink skipping).
x: Other than the above.

(3) Comprehensive Evaluation Based on the results of blocking and trapping, evaluation was made according to the following criteria.
Good: Evaluation of both blocking and trapping was "Good".
x: Other than the above.

(4) Thermal Shrinkage The films obtained in Examples and Comparative Examples were cut into samples of 100 mm MD×100 mm TD to obtain test pieces. After immersing the obtained test piece in hot water at 70°C and boiling water (100°C) for 10 seconds, the heat-shrinkable multilayer film was taken out and immersed in water at 15°C for 5 seconds. A heat shrinkage rate was determined. The shrinkage/thermal shrinkage ratio was measured using three test pieces for each example and comparative example, and the average value was used.
Thermal shrinkage rate (%) = {(100-L) / 100} x 100

According to the present invention, it is possible to suppress the deterioration of feeding performance due to adhesion between films and the adhesion of labels after label attachment, reduce ink skipping during overprinting, and prevent trapping defects. A heat-shrinkable film can be provided.

Claims (3)

A heat-shrinkable multilayer film in which front and back layers and an intermediate layer are laminated via an adhesive layer,
The front and back layers contain a polyester resin and organic fine particles,
The intermediate layer contains a polystyrene resin,
A heat-shrinkable multilayer film, wherein the content of the organic fine particles is 0.055 to 0.145 parts by weight with respect to 100 parts by weight of the polyester resin. 2. The heat-shrinkable multilayer film according to claim 1, wherein the front and back layers contain at least two kinds of organic fine particles. The front and back layers contain at least organic fine particles (A) having an average particle size of 0.5 to 2.9 μm and organic fine particles (B) having an average particle size of 3.0 to 10.0 μm. The heat-shrinkable multilayer film according to claim 2.