JP5974389B2 - Package - Google Patents

Description

  The present invention relates to a package formed by packaging an article with a synthetic resin film outer package. In particular, gums and candy boxes, tissue paper boxes, cup noodles and the like are preferably used as articles.

  Conventionally, an article having a printed layer on a surface such as paper or plastic, which is a base material of the article, is packaged with a plain synthetic resin film outer package. However, for reasons such as diversification of article forms and cost reduction, a plain container can be obtained by coating a synthetic resin film with a design by gravure printing etc. as an exterior body without printing the design directly on the article. The method of giving the design property to is adopted. The ink used for the printing layer of the outer packaging is called back printing ink because it is printed on the back side of the film.

  However, in the above method, when the synthetic resin film exterior body that has been designed by gravure printing or the like is opened and discarded, there is no printed layer on the article, which is disadvantageous from the viewpoint of design. Further, since there is no expiration date or information on goods, it is disadvantageous from the viewpoint of safety.

  For the above reasons, when packaging with a synthetic resin film having a printing layer while also having a printing layer on the surface of the substrate of the article, print on the surface of the film (the outer surface when wrapped) Is generally done.

  However, if the ink film is on the surface (outside), the ink film may be scratched by the surroundings, which is disadvantageous from the viewpoint of design.

  For the above problems, there are cases where the decrease in gloss and design properties due to overcoat varnish are suppressed, but since the number of printed layers increases further, the coating film tends to be thicker and the processability of the exterior body decreases, the synthetic resin film When the film is a shrink film, the shrinkage inhibition and blocking resistance are likely to be lowered, and the cost is increased.

  Therefore, in recent years, from the viewpoint of design properties, it is required to wrap an article having a printed layer on the surface with an exterior body having a printed layer on the back surface, but printing on the surface of the substrate of the article and the back surface of the exterior body Since the appearance is impaired due to blocking or ink scraping caused by contact between the printing layers, the article having the printing layer on the front surface is packaged with the exterior body having the printing layer on the back surface. That is avoided.

  In addition, when the exterior body is a heat-shrinkable synthetic resin film, the surface of the base material of the article and the printed layer on the back surface of the exterior body are likely to come into contact with each other due to the thermal shrinkage of the synthetic resin film. In addition, since the printing layer is softened at the heat shrink temperature at which the synthetic resin film is heat-shrinked, tack is developed, and therefore, blocking is more likely to occur and the appearance is liable to be deteriorated.

In the case of having a printed layer on the front surface or the back surface of the exterior body, there is a disadvantageous element to be adopted for the above reasons, and therefore there is a packaging material having a configuration different from the above.

After having a printed layer on the back of the exterior body, an adhesive layer is laminated, and a synthetic resin film is further laminated to avoid physical contact between the printed layers of the exterior body and the printed layers such as articles. However, the cost is high and the flexibility of the exterior body is poor. In addition, heat shrinkability cannot be imparted like a heat shrinkable synthetic resin film.

JP 2003-31723 A JP 2005-343494 A

The present invention has been made to solve the above problems, and an object of the present invention is to provide a package in which blocking does not occur between printed layers on the surface of the base material of the article and the back surface of the exterior body. is there.

Furthermore, it is providing the package which the printing layers printed on the surface of the base material of an article | item and the back surface of an exterior body rub against each other, and a printing layer does not peel off.

That is, the present invention relates to an article and a package having an exterior body on the outside thereof , and relates to a package characterized by the following (1) to ( 3 ).
(1) The article has the printing layer 1 on a part or the entire surface of the substrate , the exterior body has the printing layer 2 on the synthetic resin film, and the printing layer 2 is in contact with at least the printing layer 1. It is arranged on the surface.
(2) The printing layer 1 contains one or more resins selected from acrylic resins, cellulose resins, and urethane resins.
(3) printed layer 2, and a urethane-based resin, a vinyl chloride / vinyl acetate copolymer resin, containing from 40.7 to 100 wt% in total and acid-modified rosin resin, and the urethane resin, chloride The solid content weight ratio of the vinyl / vinyl acetate copolymer resin and the acid-modified rosin resin is 65:35 to 35:65 .

The present invention also relates to the above package, wherein the base material of the article is paper.

The present invention relates to the packaging body, wherein the exterior body is one that is heat-shrinkable.

The present invention also relates to the above package, wherein the printed layer 2 contains a surfactant and / or silicon oil.

In the package of the present invention, the printed layers provided on the base material surface of the article and the back surface of the exterior body do not block each other, so that the appearance is not impaired.

Furthermore, the printed body of the present invention does not peel off even when the printed layers printed on the surface of the substrate of the article and the back surface of the exterior body rub against each other.

Furthermore, the packaging body can maintain high designability in both the exterior body and the article.

FIG. 1 is a cross-sectional view of a package 1 in which an article is wrapped with an exterior body in which a printed layer 1 is provided on the surface of a base material of the article and a printed layer 2 is provided on the back side of the synthetic resin film. ing.

Embodiments of the present invention will be described below with reference to the accompanying drawings. As shown in FIG. 1, the package 1 is provided with a printing layer 1 containing at least one of acrylic resin, cellulose resin, and urethane resin on the side that becomes the surface of the base material of the article, and is a synthetic resin film. The printed layer 2 containing a urethane resin, a vinyl chloride / vinyl acetate copolymer resin, and / or an acid-modified rosin resin is provided on the back surface side.

The package of the present invention is used by packaging an article with a synthetic resin film. The aspect of the said packaging body can package the whole articles | goods, such as a small box of gum or a candy. Further, a part of the article can be packaged so that a part of the article, for example, a cap part of a beverage bottle or a dressing bottle is packaged. Moreover, it can also be used as what is called a multipack which packages many articles, such as a pudding container and a tissue paper box, collectively.

If the article contains contents, for example, if the article is a small box of gum, the contents are gum, and if the article is a tissue paper box, the contents are a combination of tissue paper, The package of the present invention can be used with or without the contents of the article.

Examples of items that have no contents are trading cards, comic books, etc., and can be used without problems in the present invention.

Examples of articles other than the above include containers used for cup noodles, seasonings, cosmetics, pharmaceuticals, detergents, yogurts, and the like. Other examples include articles based on paper such as books, calendars, and posters, articles based on plastics such as CD and DVD, and cases for storing these.

Specific examples of the base material of the article include glass containers, plastics such as PET, polypropylene, and paper. Paper is preferable from the viewpoints of lightness, formability, and cost.

Examples of the synthetic resin film include polyethylene terephthalate, polyester, polypropylene, polyethylene, nylon, vinyl chloride, cellophane, polylactic acid-based, foamed polyolefin-based film, stretched polyester-polystyrene co-extruded film, and polystyrene-based film.

The synthetic resin film may be any of an unstretched film, a lateral uniaxially stretched film, a longitudinal uniaxially stretched film, and a biaxially stretched film. When a heat-shrinkable synthetic resin film is used, the outer body of the synthetic resin film shrinks in accordance with the shape of the article by performing heat shrinkage treatment, so there is no gap between the article and the outer body, and the article is It is suitable for manufacturing a package that is difficult to move inside.

The heat shrinkage rate in the stretching direction of the heat-shrinkable synthetic resin film is preferably about 5 to 85%, and more preferably about 10 to 60%. By using a synthetic resin film having such a heat shrinkage rate, the effect as an exterior body can be reliably exhibited.

In addition, the average thickness of the synthetic resin film is appropriately set according to heat resistance, rigidity, mechanical suitability, appearance, and the like, and is not particularly limited. Specifically, the average thickness of the synthetic resin film is preferably about 10 to 100 μm, and more preferably about 10 to 40 μm. According to the present invention, even such a thin synthetic resin film can reliably cover an article without breaking. By this. The manufacturing cost of the package can be reduced.

In addition, various additives such as lubricants, fillers, heat stabilizers, antioxidants, UV absorbers, antistatic agents, flame retardants, and colorants are added to the synthetic resin film as necessary. May be. Further, the printed surface of the synthetic resin film may be subjected to a surface treatment such as plasma treatment, flame treatment, and acid treatment. In particular, the corona discharge treatment is used as a general surface treatment, and can improve the printability and adhesion to the printing surface of the synthetic resin film.

In addition, a synthetic resin film is not limited to the single layer film of the said film, The laminated | multilayer film of the laminated film of the 2 or more types of said film and nonwoven fabric and the said film may be sufficient. Furthermore, you may make it provide vapor deposition films, such as a silicon oxide, aluminum oxide, aluminum, on the surface and / or back surface of a synthetic resin film. When a synthetic resin film is used as a laminated film, the average thickness is preferably about 10 to 300 μm.

Next, the printing layer 1 containing at least one of acrylic resin, cellulose resin, and urethane resin will be described. The printing layer 1 can be formed from the printing ink 1 containing at least one of acrylic resin, cellulose resin, and urethane resin.

Having the printed layer 1 in any article is advantageous in terms of design. Also, if the article is a drug or food, it is necessary to describe the expiry date, information on the contents, etc., and if it is written on an exterior body that is often discarded once opened, it is said to be safer It is also advantageous from the viewpoint. In addition, depending on the article, a printing layer 1 itself is valuable, for example, a trading card or a book. For the above reason, the printing layer 1 is an essential configuration for the packaging material for the application.

The printed layer 2 is advantageous mainly from the viewpoint of design. For example, in the case where precise printing on an article is difficult due to diversification of the form and shape of the article, or when it is disadvantageous in terms of cost, the design and information are supplemented by having the printed layer 2 on the exterior body Can do. In addition, when it is desired to emphasize a new product, a notice, etc., it is easier to communicate on the printing layer 2 of the exterior body that is outside of the article. In addition, it is possible to dare to conceal or shield an article having a prize such as a trading card or an article such as food in an exterior body.

  The printing layer 1 containing at least one of the acrylic resin, the cellulose resin, and the urethane resin is obtained by printing the printing ink 1 by various printing methods such as gravure printing, flexographic printing, silk screen printing, offset printing, and inkjet. It can be formed by printing. In particular, gravure printing and flexographic printing are preferable.

Next, each resin that can be used for the printing ink 1 containing at least one of acrylic resin, cellulose resin, and urethane resin will be described.

The acrylic resin that can be used in the printing ink 1 is obtained by copolymerizing an acrylic monomer described below. Examples of the acrylic monomer include methyl acrylate, ethyl acrylate, isopropyl acrylate, and n-butyl acrylate. Acrylic acid esters such as 2-ethylhexyl acrylate; methyl methacrylate, ethyl methacrylate, isopropyl methacrylate, n-butyl methacrylate, isobutyl methacrylate, t-butyl methacrylate, cyclohexyl methacrylate, 2-ethylhexyl methacrylate And methacrylic acid esters.
One or more of these monomers can be used. In addition, copolymers with radically polymerizable monomers described below can also be used.

Crotonic acid esters such as methyl crotonate and ethyl crotonate;

Aromatic vinyls such as styrene, vinyltoluene and α-methylstyrene; Vinyl esters such as vinyl acetate and vinyl propionate and tertiary tertiary carboxylates; Heterocyclic vinyl compounds such as vinylpyrrolidone; Vinyl chloride and chloride Halogenated olefins such as vinylidene and vinylidene fluoride; vinyl ethers such as ethyl vinyl ether and isobutyl vinyl ether; vinyl ketones such as methyl vinyl ketone; α-olefins such as ethylene and propylene;

Cyano group-containing monomers such as acrylonitrile and methacrylonitrile; Dienes such as butadiene and isoprene; Amide group-containing monomers such as acrylamide, methacrylamide, maleic acid amide, and diacetone acrylamide;

Glycidyl group-containing monomers such as glycidyl methacrylate and allyl glycidyl ether;

Carboxyl group-containing monomers such as acrylic acid, methacrylic acid, maleic acid, fumaric acid, itaconic acid, mono n-butyl maleate, mono n-butyl fumarate, mono n-butyl itaconic acid, crotonic acid;

(Meth) acrylic acid 2-hydroxyethyl, (meth) acrylic acid 2-hydroxypropyl, (meth) acrylic acid 3-hydroxypropyl, (meth) acrylic acid 4-hydroxybutyl, acrylic acid (2-hydroxymethyl) ethyl, Acrylic acid (2-hydroxymethyl) butyl, (meth) acrylic acid (4-hydroxymethylcyclohexyl) methyl, glycerin mono (meth) acrylate, 2- (meth) acryloyloxyethyl 2-hydroxypropyl phthalate, 2-hydroxy-3 -(Meth) acrylic acid esters containing hydroxyl groups such as phenoxypropyl (meth) acrylate; allyl compounds containing hydroxyl groups such as allyl alcohol and 2-hydroxyethyl allyl ether;

Vinyl ether compounds containing a hydroxyl group such as 2-hydroxyethyl vinyl ether, 4-hydroxybutyl vinyl ether, 6-hydroxyhexyl vinyl ether; unsaturated carboxylic amides having a hydroxyl group such as N-methylol (meth) acrylamide and N-methylolcrotonamide Compound;

Hydroxyl group-containing unsaturated fatty acids such as ricinoleic acid;
Hydroxyl group-containing unsaturated fatty acid esters such as alkyl ricinoleate;

Monomers obtained by addition reaction of hydroxyl group-containing monomers with alkylene oxides such as ethylene oxide and propylene oxide;

Tertiary amino group-containing monomers such as dimethylaminoethyl methacrylate and diethylaminoethyl methacrylate;

Vinyltrimethoxysilane, vinyltriethoxysilane, vinyltriisopropoxysilane, vinyltris (β-methoxyethoxy) silane, vinylmethyldimethoxysilane, vinylmethyldiethoxysilane, vinyldimethylmethoxysilane, vinyldimethylethoxysilane, 3-methacryloxy Alkoxysilyl group-containing monomers such as propyltrimethoxysilane, 3-methacryloxypropyltriethoxysilane, 3-methacryloxypropylmethyldimethoxysilane, 3-methacryloxypropylmethyldiethoxysilane;

Examples thereof include monomers having two or more unsaturated bonds in one molecule, such as diallyl phthalate, divinylbenzene, allyl acrylate, and trimethylolpropane trimethacrylate.

The acrylic resin has a weight average molecular weight of 20,000 to 130,000, and particularly preferably 30,000 to 110,000. When it is within the above range, the coating film strength is improved, and the adhesive strength and friction resistance are improved. Further, it is preferable because an appropriate viscosity is easily maintained and handling is improved.

Moreover, it is preferable that Tg of acrylic resin is 20 to 150 degreeC, More preferably, it is 30 to 80 degreeC. When the acrylic resin has a Tg of 20 ° C. or higher, the acrylic resin has sufficient hardness at room temperature, which is preferable from the viewpoint of blocking resistance. Furthermore, it is preferable that Tg is 150 ° C. or lower because an appropriate viscosity is easily maintained and handling is improved.

Further, the acrylic resin is preferably dissolved or dispersed in an alcohol-based or ester-based organic solvent from the viewpoint of drying of printed matter. The alcohol solvent is preferably one of methanol, ethanol, isopropanol, and normal propanol, or a mixed solvent thereof, and the ester solvent is any one of ethyl acetate or normal propyl acetate, or a mixed solvent thereof. It is preferable.

Further, in the printing ink 1, it is possible to use a water-soluble acrylic resin emulsion.
Emulsions of water-soluble acrylic resins can be copolymerized with styrenic monomers and / or methyl methacrylate as needed in the presence of polymer emulsifiers with carboxyl or anhydride groups in the molecule. This is an aqueous resin emulsion obtained by emulsion polymerization by adding a radically polymerizable monomer. As the polymer emulsifier of the present invention, at least one of acrylic resin, styrene-acrylic resin, and styrene-acrylic-maleic acid resin can be used.

Here, acrylic resin, styrene-acrylic resin, and styrene-acrylic-maleic acid resin are copolymer resin of acrylic monomer, copolymer of styrene monomer and acrylic monomer, respectively. It is a three-component copolymer resin of a resin and a styrene monomer, an acrylic monomer, and a maleic monomer. Furthermore, an acrylic monomer, a styrene monomer, and a maleic acid monomer are monomer components shown below.

Acrylic monomer: (meth) acrylic acid, alkyl ester having 1 to 18 carbon atoms, alkyl amide having 1 to 18 carbon atoms, hydroxyalkyl ester having 2 to 4 carbon atoms, and the like Are methyl (meth) acrylate, ethyl (meth) acrylate, butyl (meth) acrylate, hexyl (meth) acrylate, octyl (meth) acrylate, lauryl (meth) acrylate, stearyl (meth) acrylate, methyl ( Examples include meth) acrylamide, ethyl (meth) acrylamide, butyl (meth) acrylamide, hexyl (meth) acrylamide, and 2-hydroxyethyl (meth) acrylate, and the above acrylic monomer bodies can also be used. .

Styrene monomer: Styrene and its derivatives. Specific examples include α-methylstyrene, chlorostyrene, vinyltoluene and the like. -Maleic acid monomer: (anhydrous) maleic acid and its alkyl ester having 1 to 18 carbon atoms, alkyl amide having 1 to 18 carbon atoms, hydroxyalkyl ester having 2 to 4 carbon atoms, etc. Specifically, these monomers such as monomethylmalate, dimethylmalate, monoethylmalate, diethylmalate, monobutylmalate, monooctylmalate, mono-2-hydroxyethylmalate are copolymerized. The obtained polymer emulsifier has an acid value of 80 to 300, preferably 150 to 250, and a number average molecular weight of 3,000 to 200,000, preferably 10,000 to 100,000.

It is preferable that the acid value of the water-soluble polymer emulsifier is in the above range because the water resistance of the ink is improved. In addition, since the action as a polymer emulsifier is sufficiently exhibited and the solubility of the polymer emulsifier in water can be sufficiently ensured, the printing effect is improved.

Examples of the alkali compound used for dissolving the polymer emulsifier in water include ammonia, organic amines, alkali metal hydroxides, and the like. Specifically, as the organic amine, diethylamine, triethylamine, ethylenediamine, etc. Examples of the alkylamine, monoethanolamine, ethylethanolamine, diethylethanolamine, diethanolamine, triethanolamine and other alkanolamines and alkali metal hydroxides include sodium hydroxide and potassium hydroxide. Among them, those that readily volatilize at normal temperature or slight heating are desirable in order to improve drying properties.

The required amount of the alkali compound is the amount necessary to allow the polymer emulsifier to exist stably in water, with the lower limit being about 80% of the neutralization amount and the upper limit being about twice the neutralization amount. It is. On the other hand, the radical polymerizable monomer (emulsion polymerization component) used in emulsion polymerization in the presence of the polymer emulsifier can be used alone or in combination with the styrene monomer and methyl methacrylate. Further, if necessary, other copolymerizable acrylic acid or methacrylic acid ester can be used in combination up to 30% by weight of the total monomers used in the emulsion polymerization.

In addition, as a method for producing an emulsion of a water-soluble acrylic resin using the above-described polymer emulsifier, alkali compound, and radical polymerizable monomer used in emulsion polymerization as an emulsion polymerization component, first, acetic acid is used. Monomer component for obtaining a polymer emulsifier in the presence of a polymerization initiator in an organic solvent such as an ester solvent such as ethyl or isopropyl acetate, a ketone solvent such as acetone or methyl ethyl ketone, a lower alcohol solvent, glycol or a derivative thereof. Then, the organic solvent is distilled off to obtain a solid resin soluble in an alkaline aqueous solution.

Next, in the presence of an alkali compound, the solid resin is dissolved in water to form a water-soluble polymer emulsifier, and a mixture of a radical polymerizable monomer and a polymerization initiator used in emulsion polymerization is added dropwise to effect emulsion polymerization. A method for obtaining a water-soluble acrylic resin emulsion can be used. Examples of the polymerization initiator include persulfates such as potassium persulfate, sodium persulfate, and ammonium persulfate, organic peroxides such as benzoyl hydroperoxide, and azo compounds such as azobisisobutyronitrile. It can also be used as a redox initiator in combination with a reducing agent as required.

The water-soluble acrylic resin emulsion obtained by emulsion polymerization needs to have a glass transition temperature of 20 ° C. or higher. When the glass transition temperature of the polymer is 20 ° C. or higher, the emulsion particles are easily formed into a film in the drying process and the like, and an ink having good gloss can be obtained. In the emulsion of the water-soluble acrylic resin, the weight ratio of the water-soluble polymer emulsifier to the polymer obtained by emulsion polymerization is 8 to 40% by weight of the polymer emulsifier emulsion. The combined amount is 60 to 92% by weight.

When the weight ratio of the polymer emulsifier falls within the above range, the dispersion stability of the water-soluble acrylic resin emulsion in water and the fluidity of the ink are improved, so that the gloss of the ink is improved. Further, the average particle size of the water-soluble acrylic resin emulsion is in the range of 30 to 150 nm, more preferably 80 to 120 nm. When the average particle diameter of the water-soluble acrylic resin emulsion is within the above range, the ink concealing property and density feeling are improved, and the gloss and printability of the ink are favorable.

Furthermore, in the printing ink 1, an active energy ray-curable acrylic resin can be used.

The printing layer 1 can be laminated | stacked with the printing ink 1 which has the said active energy ray-curable acrylic resin.

By laminating the printing layer 1 having an active energy ray-curable acrylic resin on the outermost layer, the surface protection and the surface of the substrate of the article are resistant to stains, cellophane tape, chemical resistance, etc. Embossing, gloss, etc. can be given greatly.

The printing ink 1 having the active energy ray curable acrylic resin is an active energy ray curable acrylic by printing by various printing methods such as gravure printing, flexographic printing, silk screen printing, offset printing, and inkjet. The printing layer 1 which has a system resin can be formed. In particular, offset printing is preferable in terms of design, and silk screen printing is preferable in terms of embossing because of the large amount of coating.

The active energy ray-curable acrylic resin has an ethylenically unsaturated double bond that is radically polymerized and cured by energy rays such as ultraviolet rays and electron beams.

The active energy ray-curable acrylic resin is composed of an oligomer and a monomer, and the oligomer imparts resistance and flexibility to the surface protective layer and is measured by number average molecular weight (gel permeation chromatography (GPC). The same shall apply.) Those of 1000 or more are preferably used. Examples thereof include urethane acrylate having a (meth) acrylate group, polyester acrylate, acrylic acrylate, epoxy acrylate and the like. Of these, urethane acrylate is preferred because it is expected to provide flexibility as well as adhesion to the base.

Among the active energy ray-curable acrylic resins, the monomer is added for the purpose of improving the physical properties of the surface protective layer and adjusting the viscosity of the active energy ray-curable composition, and is a monomer having a (meth) acrylate group. Examples include functional, bifunctional, and polyfunctional monomers.

Monofunctional monomers include 2- (2-ethoxyethoxy) ethyl acrylate, stearyl acrylate, tetrahydrofurfuryl acrylate, lauryl acrylate, 2-phenoxyethyl acrylate, indecyl acrylate, isooctyl acrylate, tridecyl acrylate, caprolactone acrylate, 4 -Hydroxybutyl acrylate, ethoxylated noniphenol acrylate, propoxylated nonylphenol acrylate, phenoxyethyl acrylate, phenoxydiethylene acrylate, ethylene oxide modified nonylphenyl acrylate, methoxytriethylene glycol acrylate, ethylene oxide 2-ethylhexyl acrylate, isobornyl acrylate, di Propylene glycol acrylic It includes over preparative, or the like, or methacrylate monomers.

As the bifunctional monomer, 1,3-butanediol diacrylate, 1,4-butanediol diacrylate, polyethylene glycol diacrylate, polypropylene glycol diacrylate, neopentyl glycol diacrylate, propoxylated neopentyl glycol diacrylate, ethoxylation Neopentyl glycol diacrylate, hydroxypivalate neopentyl glycol diacrylate, (hydrogenated) bisphenol A diacrylate, (hydrogenated) ethylene oxide modified bisphenol A diacrylate, (hydrogenated) propylene glycol modified bisphenol A diacrylate, 1, 6-hexanediol diacrylate, 2-ethyl, 2-butyl-propanediol diacrylate, 1,9-nonanedio Diacrylate and those methacrylate monomers.

Examples of polyfunctional monomers include tris (2-hydroxyethyl) isocyanurate triacrylate, ethylene oxide modified trimethylolpropane triacrylate, propylene oxide modified trimethylolpropane triacrylate, propylene oxide modified glyceryl triacrylate, pentaerythritol triacrylate, trimethylol. Propane acrylate, ethylene oxide modified trimethylolpropane acrylate, propylene oxide modified trimethylolpropane acrylate, tris (acryloxyethyl) isocyanurate, pentaerythritol tetraacrylate, ditrimethylolpropane tetraacrylate, dipentaerythritol hydroxypentaacrylate, ethoxylated pentaerythris Lito And tetramethacrylate monomers, pentaacrylate esters, dipentaerythritol hexaacrylate and the like, and methacrylate monomers thereof.
Among these monomers, ethylene oxide-modified trimethylolpropane triacrylate is particularly preferable from the viewpoint of cellophane tape releasability and cost. Examples of the ethylene oxide-modified trimethylol acrylate include those having 1 to 20 mol of ethylene oxide repeating units (expressed as mol-modified), among which the physical properties of the film in which 3 to 9 mol-modified are crosslinked. Excellent and preferable.

The active energy ray-curable acrylic resin is used in an amount of 60 to 95% by weight in the printing ink 1 having the active energy ray-curable acrylic resin. If it is less than 60% by weight, the physical properties of the film deteriorate, and if it is more than 95% by weight, it is difficult to sufficiently exhibit the cellophane tape peelability. Further, in the active energy ray-curable acrylic resin, it is preferable from the viewpoint of film properties that the oligomer is 0 to 80% by weight and the monomer is 20 to 100% by weight.

When the radically polymerizable crosslinking component is crosslinked with ultraviolet rays, examples of the photopolymerization initiator include acetophenones, benzophenones, thioxanthones, aromatic diazonium salts, and metallocenes. In addition, amines and phosphines can be used in combination as polymerization accelerators. In the case of crosslinking with an electron beam, these may not be blended.
In addition, when the cationically reactive component is cross-linked by ultraviolet rays, the cationic initiator includes Lewis acid diazonium salt, Lewis acid iodonium salt, Lewis acid sulfonium salt, Lewis acid phosphonium salt, and other halogens. Compounds, triazine-based initiators, borate-based initiators, and other photoacid generators. In the case of crosslinking with an electron beam, these may not be blended.

The printing ink 1 having an active energy ray-curable acrylic resin can be further blended with an organic / inorganic filler as necessary, and can impart gloss adjustment and wear properties. For example, resins such as epoxy resin, melamine resin, urea resin, acrylic resin, polyimide resin, Teflon resin (registered trademark), polyethylene resin, polyester resin, polyester resin, polyamide resin are polymerized until they are insoluble in the solvent. Examples include inorganic fillers such as finely divided organic fillers, alumina, talc, magnesium carbonate, calcium carbonate, natural mica, synthetic mica, aluminum hydroxide, precipitated barium sulfate, precipitated barium carbonate, barium titanate, and barium sulfate. .

The active energy ray-curable acrylic resin composition can be blended with a colorant and various additives as required, for example, a leveling agent, an antifoaming agent, a slipping agent, and the like. Not.

Next, the cellulose-based resin that can be used in the printing ink 1 is a material well known to have good solubility even in an organic solvent system that does not contain an aromatic hydrocarbon. For example, when a nitro group-substituted product having a high glass transition temperature and a hard film is used, an ink composition excellent in blocking resistance and heat resistance can be obtained.

Cellulose acetate, cellulose acetate propionate, cellulose acetate butyrate and the like are obtained by reacting cellulose with a suitable organic acid / acid anhydride. That is, cellulose is mixed with an appropriate organic acid / acid anhydride / catalyst and reacted until a triester is formed. After complete acylation, it is hydrolyzed to the desired hydroxyl level. Cellulose acetate is obtained by triesterification with acetic acid and then hydrolysis. Generally, acetylation is 0.6-2. A resin having 5% by weight and a hydroxyl group of 1.8 to 5% is commercially available. Cellulose acetate propionate is obtained by triesterification with acetic acid and propionic acid, followed by hydrolysis. Generally, a resin having 0.6 to 2.5% by weight of acetylation, 42 to 46% by weight of propionation, and 1.8 to 5% of hydroxyl group is commercially available. Cellulose acetate butyrate is obtained by triesterification with acetic acid and butyric acid, followed by hydrolysis. Generally, a resin having 2 to 30% by weight of acetylation, 17 to 53% by weight of butyrylation, and 1 to 5% of hydroxyl group is commercially available.

Nitrocellulose can be obtained by esterifying part or most of the hydroxyl groups of cellulose with nitric acid. Nitrocellulose has resins with various degrees of polymerization, and generally products having an average degree of polymerization of 35 to 480 are commercially available. The cellulosic resin can be used as a mixture.

As for the molecular weight of these cellulose resins and the degree of substitution with respect to hydroxyl groups, those in the range used in ordinary ink compositions and paints can be used without any problem in the present invention. Also, the use of a nitro group-substituted product is advantageous from the viewpoint of heat resistance, and the lower acyl group-substituted product and lower alkyl group-substituted product are advantageous from the viewpoint of adhesiveness. It is preferable to use it.

Solvents that can be used for the cellulose resin include ester solvents such as ethyl acetate, n-propyl acetate, isopropyl acetate, isobutyl acetate, propylene glycol monoethyl ether acetate, methanol, ethanol, n-propanol, isopropanol, n-butanol, and the like. These alcohol solvents, aromatic solvents such as benzene, toluene and xylene, ketone solvents such as acetone, methyl ethyl ketone and methyl isobutyl ketone, and known solvents such as water can be used alone or in combination.

The urethane resin that can be used in the printing ink 1 has good solubility even in an organic solvent system that does not contain an aromatic hydrocarbon, has a good printing effect, and can form a flexible coating film. Urethane resin uses a polymer polyol and diisocyanate, if necessary, an inert solvent for the isocyanate group and, if necessary, a reaction with a urethanization catalyst at a temperature of 10 to 150 ° C., and is terminated with an isocyanate group. And then reacting this prepolymer with a chain extender and a terminal terminator to obtain a urethane resin, or reacting a polymer polyol, diisocyanate and chain extender in one step. Thus, it can be produced by a known method such as a one-shot method for obtaining a urethane resin.

Examples of the polymer polyol include polyester polyol, polyether polyol, and acrylic polyol. In the present invention, it is desirable to use one or more of polyester polyol and polyether polyol.

The polyester polyol is a polyester polyol containing a hydroxyl group at the terminal and / or side chain, and is obtained by dehydration condensation or polymerization of a hydroxyl group-containing compound such as glycol or polyol and a polyvalent carboxylic acid or an anhydride thereof. can get. In the present invention, more specifically, a polyester diol composed of a compound containing two hydroxyl groups and a divalent carboxylic acid is preferred.

Examples of the hydroxyl group-containing compound used for the synthesis of the polyester polyol include ethylene glycol, 1,2-propanediol, 1,3-propanediol, 1,3-butanediol, pentanediol, and 2-methyl-1,3-propane. Diol, neopentyl glycol, 3-methyl-1,5-pentanediol, hexanediol, octanediol, 1,9-nonanediol, 2-methyl-1,8-octanediol, 1,4-butynediol, 2 , 2,4-Trimethyl-1,3-pentanediol, 1,4-cyclohexanedimethanol, 2-butyl-2-ethyl-1,3-propanediol, 3-methyl 1,5-pentanediol, diethylene glycol, triethylene Glycol, polypropylene glycol, dipropylene glycol Call. Moreover, the low molecular polyol which has 3 or more of hydroxyl groups, such as glycerol, a trimethylol propane, a trimethylol ethane, 1,2, 6-hexane triol, 1,2, 4- butane triol, sorbitol, a penta esitol, is also mentioned. .

In addition, as a high molecular weight hydroxyl group-containing compound, saturated or unsaturated low molecular weight diols, polymers such as ethylene oxide, propylene oxide, and tetrahydrofuran or copolymer polyether diols are also used as raw materials for polyester diols. can do.

Furthermore, it is preferable to use a hydroxyl group-containing compound having an alkyl side chain as a monomer for the polyester polyol. By using the polyester polyol, the crystallinity of the urethane-based resin is greatly lowered, and the alkyl side chain is hydrocarbon and hydrophobic, so that the adhesion to the polyolefin film is improved. Furthermore, hydrolysis resistance improves compared with the case where a hydroxyl-group containing compound does not have an alkyl side chain.

Polycarboxylic acid monomers used for the synthesis of polyester diol include adipic acid, phthalic acid, isophthalic acid, terephthalic acid, maleic acid, fumaric acid, succinic acid, oxalic acid, malonic acid, glutaric acid, pimelic acid, speric acid, Examples thereof include polycarboxylic acids such as azelaic acid, sebacic acid, trimellitic acid and pyromellitic acid, and anhydrides (4) thereof. Among these, it is preferable to use adipic acid from the viewpoint of solubility in a non-toluene solvent, and it is more preferable to use 50% by weight or more in the polyvalent carboxylic acid monomer.

The number average molecular weight of the polyester diol used for the urethane resin is appropriately determined in consideration of the solubility, drying property, blocking resistance and the like of the obtained urethane resin, and is usually in the range of 400 to 100,000, preferably 400 to 6000. It should be inside. If the number average molecular weight is within the above range, the hard segment becomes an appropriate amount, and sufficient solubility can be secured, so that the printing effect is good. Moreover, since there exists a tendency which drying property and blocking resistance improve, it is preferable.

The acid value of the polyester diol is preferably 1.0 mgKOH / g or less, and more preferably 0.5 mgKOH / g or less. This is because if the acid value is larger than 1.0 mg KOH / g, the tendency of the printing ink to increase in viscosity increases.

The polyester diol is superior to other polymer polyols in blocking resistance, and is preferably used in an amount of 50% by weight or more in the polymer polyol in total of the polyester polyols.

It is also preferable to use a polyether polyol as the polymer polyol. For example, polyethylene glycol, polypropylene glycol, polytrimethylene glycol, polytetramethylene glycol and the like can be mentioned. Since these have excellent solubility in alcohol and can impart another solvent solubility to the polyester-based polyurethane, they are preferably used in combination in many applications. The polyether polyol molecular weight is preferably 400 to 3000 in order to develop these characteristics and not lower water resistance.

Examples of the diisocyanate used for the synthesis of the urethane resin include various known aromatic diisocyanates, aliphatic diisocyanates, and alicyclic diisocyanates that are generally used in the production of urethane resins. For example, 1,5-naphthylene diisocyanate, 4,4′-diphenylmethane diisocyanate (MDI), 4,4′-diphenyldimethylmethane diisocyanate, 4,4′-dibenzyl isocyanate, dialkyldiphenylmethane diisocyanate, tetraalkyldiphenylmethane diisocyanate, 1 , 3-phenylene diisocyanate, 1,4-phenylene diisocyanate, tolylene diisocyanate, butane-1,4-diisocyanate, hexamethylene diisocyanate, isopropylene diisocyanate, methylene diisocyanate, 2,2,4-trimethylhexamethylene diisocyanate, lysine diisocyanate, Cyclohexane-1,4-diisocyanate, xylylene diisocyanate, isophorone diisocyanate Nate, dimethylene diisocyanate, dicyclohexylmethane-4,4′-diisocyanate, 1,3-bis (isocyanatemethyl) cyclohexane, methylcyclohexane diisocyanate, norbornane diisocyanate, m-tetramethylxylylene diisocyanate, bis-chloromethyl-diphenylmethane-diisocyanate 2,6-diisocyanate-benzyl chloride, dimerized isocyanate obtained by converting a carboxyl group of dimer acid into an isocyanate group, and the like. These diisocyanate compounds can be used alone or in admixture of two or more.

A chain extender may be used for the synthesis of the urethane resin. For example, in addition to 2-butyl-2-ethyl-1,3-propanediol, the saturated or unsaturated low molecular polyols, ethylenediamine, propylenediamine, and the like. , Hexamethylenediamine, diethylenetriamine, triethylenetetramine, isophoronediamine, dicyclohexylmethane-4,4′-diamine, 2-hydroxyethylethylenediamine, 2-hydroxyethylpropyldiamine, 2-hydroxyethylpropylenediamine, di-2 -Hydroxyethylethylenediamine, di-2-hydroxyethylenediamine, di-2-hydroxyethylpropylenediamine, 2-hydroxypyrroleethylenediamine, di-2-hydroxypyrroleethylenediamine, di-2-hydride Amines having a hydroxyl group in the molecule such as hydroxypropyl ethylenediamine can also be used. These chain extenders can be used alone or in admixture of two or more.

A monovalent active hydrogen compound can also be used as a terminal terminator for the purpose of terminating the reaction. Examples of such compounds include compounds having primary and secondary amino groups, dialkylamines such as di-n-butylamine, amino alcohols having a hydroxyl group, and alcohols such as ethanol and isopropyl alcohol. Furthermore, amino acids such as glycine and L-alanine can be used as a reaction terminator particularly when it is desired to introduce a carboxyl group into the urethane resin. Among these, amino alcohols having primary and secondary amino groups need to be controlled so as to react only with amino groups while avoiding reaction at high temperature when used as a terminal terminator. These end terminators can be used alone or in admixture of two or more. Here, when an amino group is used as the chain extender, it reacts with an isocyanate group to form a urea bond, so that the resulting resin is a polyurethane / urea resin. In the present invention, these resins are also urethane-based resins. And

  Furthermore, in the present invention, a water-soluble urethane resin can also be used. When synthesizing a water-soluble urethane-based resin, an anionic group-containing compound having an active hydrogen group, a cationic group-containing compound, a nonionic group-containing compound, or the like is used in addition to the polymer polyol and diisocyanate. . In the present invention, it is preferable to use an anionic group-containing compound and use a nonionic group-containing compound in combination as necessary from the viewpoints of solubility of the water-soluble urethane resin, physical properties of the coating film, and the like.

As an anionic group-containing compound having an active hydrogen group, a compound having a carboxyl group is generally known, and 2,2-dimethylolpropionic acid, 2,2-dimethylolbutanoic acid, 2-dimethylolbutyric acid, 2, Dimethylolalkanoic acid such as 2-dimethylolvaleric acid, glutamine, asparagine, lysine, diaminopropionic acid, ornithine, diaminobenzoic acid, diamine type amino acids such as diaminobenzenesulfonic acid, glycine, alanine, glutamic acid, taurine, aspartic acid, Monoamine type amino acids such as aminobutyric acid, valine, aminocaproic acid, aminobenzoic acid, aminoisophthalic acid, sulfamic acid and the like can be mentioned.

The anionic group incorporated in the urethane resin forms a salt by neutralization and dissolves in water. Examples of the neutralizing agent used in this case include ammonia, monoethylamine, diethylamine, trimethylamine, triethylamine, triisopropylamine, tributylamine, triethanolamine, methyldiethanolamine, and monoethanolamine. Ammonia is preferred because it does not easily remain in the film and does not impair the physical properties of the coating.

Examples of the cationic group-containing compound having an active hydrogen group include compounds having an amino group, an ammonium base, a sulfonium base and the like. However, the cationic group incorporated in the urethane-based resin is dissolved in water by neutralization, but often has to use inorganic ions such as sodium ion and lithium ion as the neutralizing agent. Since the neutralizing agent remains, it is not preferable in terms of physical properties of the coating film.

As the nonionic group-containing compound, it is preferable to use an ethylene oxide repeating unit-containing compound such as ethylene glycol or polyethylene glycol. Since the nonionic group has poor solubility in water, it is difficult to dissolve the urethane resin in water with only the nonionic group. However, in order to adjust the stability of the resin and the suitability of the coating film, the anion / It can be used in combination with a cationic group-containing compound.

In the production of the prepolymer which is an intermediate of the urethane resin, the amount of the polymer polyol and diisocyanate is the ratio of the number of moles of the isocyanate group of the diisocyanate to the total number of moles of the diol containing the polymer polyol and the hydroxyl group of the polyol. The NCO / OH ratio is preferably in the range of 1.1 to 3.0. When this ratio is less than 1.1, there is a tendency that sufficient alkali resistance cannot be obtained, and when it is more than 3.0, the solubility of the resulting prepolymer tends to be lowered.

Furthermore, a catalyst can also be used for this urethanation reaction. Examples of catalysts that can be used include tertiary amine catalysts such as triethylamine and dimethylaniline; metal catalysts such as tin and zinc. These catalysts are used in the range of 0.001 to 1 mol% with respect to the hydroxyl group-containing compound including the polymer polyol.

The above-obtained prepolymer having an isocyanate group at the terminal and a chain extender such as diol, diamine, or triol are reacted at 10 to 80 ° C. to obtain a urethane resin containing an active hydrogen group at the terminal.

When using an end-stopper, the end-stopper and chain extender may be used together to carry out a chain extension reaction. Thus, an end termination reaction may be performed. On the other hand, the molecular weight can be controlled without using a terminal terminator, but in this case, a method of adding a prepolymer to a solution containing a chain extender is preferable in terms of reaction control.

End terminators are used to control molecular weight. When the amount used is increased, the molecular weight of the urethane resin obtained is lowered. This varies depending on the reactivity of the chain extender and end terminator to the prepolymer, but in general, the ratio of the number of moles of amino groups and hydroxyl groups of the chain extender to the number of moles of amino groups and hydroxyl groups of the end terminator is A range of 0.5 to 5.0 is preferred. When this ratio exceeds 5.0, the polymer has a high molecular weight, so that the suitability for dry lamination tends to deteriorate. When it is less than 0.5, the molecular weight and the initial adhesive force tend to decrease.

The ratio of the total number of moles of amino groups and hydroxyl groups of the chain extender and terminal terminator to the equivalent of isocyanate groups in the prepolymer is 1.1 to 3.0, preferably 1.5 to 2.0. To react. When this ratio is large and the amount of chain extender or terminal terminator used is large, they remain unreacted and odor tends to remain.

The urethane resin preferably has a weight average molecular weight of 13,000 to 60,000. Within the above range, the blocking resistance in the printed material can be ensured, and the solubility in a solvent can be sufficiently ensured, so that the printing effect is good, which is preferable.

The amine value of the urethane-based resin is preferably 0.5 to 14.0 mgKOH / g, and the amine value is more preferably 5.0 to 10.0 mgKOH / g. Within the above range, it is preferable because adhesion to the polyolefin film can be ensured and the ink stability when an isocyanate curing agent is added is good.

Examples of the solvent used in the urethane resin include ester solvents such as ethyl acetate, n-propyl acetate, isopropyl acetate, isobutyl acetate, propylene glycol monoethyl ether acetate, methanol, ethanol, n-propanol, isopropanol, n- Alcohol solvents such as butanol, aromatic solvents such as benzene, toluene and xylene, ketone solvents such as acetone, methyl ethyl ketone and methyl isobutyl ketone, and known solvents such as water can be used alone or in combination.

The printing ink 1 can be used in combination with an isocyanate curing agent depending on the application, base material, and necessary physical properties. As an example of the isocyanate curing agent to be used, diisocyanate includes hexamethylene diisocyanate (HDI), isophorone diisocyanate (IPDI), and xylylene diisocyanate (XDI). Examples of the modified polyisocyanate include adduct type, bifunctional prepolymer type, and biuret type. From the viewpoint of inhibiting heat shrinkage of the heat-shrinkable film, it is desirable that the diisocyanate is selected from HDI and IPDI, and the modified polyisocyanate is selected from an adduct type and a bifunctional prepolymer. These curing agents can be used alone or in admixture of two or more, and preferably 1 to 10% by weight in 100 parts by weight of the printing ink 1. When it is within the above range, blocking resistance can be ensured by improving the drying property of the printed matter.

Next, the printing layer 2 containing a urethane resin and a vinyl chloride / vinyl acetate copolymer resin and / or an acid-modified rosin resin will be described. The printing layer 2 can be formed from a printing ink 2 containing a urethane resin and a vinyl chloride / vinyl acetate copolymer resin and / or an acid-modified rosin resin.

Printing ink 2 containing urethane resin and vinyl chloride / vinyl acetate copolymer resin and / or acid-modified rosin resin is available in various printing methods such as gravure printing, flexographic printing, silk screen printing, offset printing, and inkjet printing. The printing layer 2 can be formed by printing. In particular, gravure printing and flexographic printing are preferable.

The vinyl chloride / vinyl acetate copolymer resin is obtained by copolymerizing a vinyl chloride monomer and a vinyl acetate monomer. The vinyl chloride / vinyl acetate copolymer having a hydroxyl group can further use vinyl alcohol in the copolymerization or saponify a part of vinyl acetate. In the vinyl chloride / vinyl acetate copolymer having a hydroxyl group, the properties of the resin film and the resin dissolution behavior are determined by the monomer ratio of vinyl chloride, vinyl acetate and vinyl alcohol. That is, vinyl chloride gives the toughness and hardness of the resin film, vinyl acetate gives adhesion and flexibility, and vinyl alcohol is soluble in polar solvents and compatible with urethane resins and acid-modified rosin resins. And the friction resistance is improved. In the present invention, the vinyl chloride / vinyl acetate copolymer preferably has a hydroxyl group.

The softening point of the vinyl chloride / vinyl acetate copolymer resin is preferably 60 ° C to 90 ° C. It is desirable for it to be within the range of the previous period because it is excellent in blocking resistance between printed layers.

The acid-modified rosin resin is generally derived from conifers and other plants, and includes (but is not limited to) maleic acid, phthalic acid, neoabietic acid, pulpstriic acid, pimaric acid, levopimaric acid, isopimaric acid, dehydro A generic term for rosins and their esters that have been modified by reacting an acid or anhydride with rosin containing a mixture of organic acids such as abietic acid and related compounds and isomers, including abietic acid, sandaracopimalic acid, etc. .

The acid-modified rosin-based resin has advantages that the softening point is high to some extent, the blocking resistance between printed layers is excellent, and the adhesiveness to the plastic film is high.

The acid value of the acid-modified rosin is preferably 10 to 110 mgKOH / g. More preferably, it is 10-85 mgKOH / g, and when it is in the said range, since the solubility to a solvent and blocking resistance become favorable, it is desirable.

The softening point of the acid-modified rosin is preferably 100 ° C to 200 ° C. If it is within the range of the previous period, it is desirable because it is excellent in friction resistance and heat blocking resistance between the printing layers.

The urethane resin that can be used in the printing ink 2 containing the urethane resin and the vinyl chloride / vinyl acetate copolymer resin and / or the acid-modified rosin resin is the vinyl chloride / vinyl acetate copolymer resin or acid. A urethane resin that has good compatibility with the modified rosin resin and can be used in the printing ink 1 can be used.

The urethane resin is a well-known material having good solubility even in an organic solvent system that does not contain an aromatic hydrocarbon. For example, although it is not a resin with a very high softening point, having a hard segment has an advantage of excellent blocking resistance between printed layers and high adhesion to a plastic film.

In the organic solvent system that does not contain aromatic hydrocarbons, as a result of intensive research to obtain a printing ink 2 that is excellent in adhesion and various resistances while maintaining high printing quality, the present inventors have developed The present invention has been completed by finding that the required performance can be further improved by combining a resin with a vinyl chloride / vinyl acetate copolymer resin and / or an acid-modified rosin resin at a specific composition ratio. It is.

Accordingly, the printing ink 2 is characterized by containing a urethane resin as a binder resin and a vinyl chloride / vinyl acetate copolymer resin and / or an acid-modified rosin resin.

The printing ink 2 is composed of urethane resin, vinyl chloride / vinyl acetate copolymer resin and / or acid-modified rosin resin from the viewpoints of adhesion to the synthetic resin film and blocking resistance and heat blocking resistance to the printing ink 1. It is necessary to use urethane resin: vinyl chloride / vinyl acetate copolymer resin and / or acid-modified rosin resin in an amount of a solid content weight ratio of 75:25 to 25:75. In particular, urethane resin: vinyl chloride / vinyl acetate copolymer resin and / or acid-modified rosin resin is a vinyl chloride / vinyl acetate copolymer resin and / or acid-modified rosin resin from a solid weight ratio of 65:35. In view of blocking resistance of the printing layer 2 with respect to the printing layer 1, it is preferable and preferable to contain a large amount. In addition, the urethane-based resin: vinyl chloride / vinyl acetate copolymer-based resin and / or the acid-modified rosin-based resin contains more urethane-based resin than the solid content weight ratio of 35:65, so that the adhesiveness to the plastic film is improved. Are particularly preferred. When all three types of urethane resin, vinyl chloride / vinyl acetate copolymer resin and acid-modified rosin resin are used in combination with the above composition ratio, it is particularly preferable because high physical properties can be maintained in adhesiveness and heat blocking resistance. . The combined content of both resins in the ink composition is appropriately 5 to 55% by weight as the solid content.

In addition, when the synthetic resin film has heat shrinkability, the above ratio maintains the adhesiveness to the synthetic resin film and the followability to the film, so that the shrinkage of the synthetic resin film is inhibited during the heat shrinkage. There is nothing to do. Moreover, although the conditions under which the synthetic resin is thermally shrunk depend on the type and thickness of the synthetic resin film, it is usually about 0.3 to 10.0 seconds at 80 to 240 ° C. However, the printing layer 2 is softened at that time. It is difficult to block between the printing layer 1 and the heat.

Printing ink 2 containing the urethane resin and vinyl chloride / vinyl acetate copolymer resin and / or acid-modified rosin resin (printed layer 2 after being applied to a synthetic resin film) is printed as necessary. Silicon oil, a surfactant or the like can be added as a release agent for further improving the blocking resistance, heat blocking resistance, sliding property, and friction resistance with the layer 1.

As the silicone oil, either a silicone resin having an amino group or a silicone resin not having an amino group can be used. As the silicone resin having an amino group, any one of primary, secondary, and tertiary amino groups can be used. In the present invention, primary or secondary is preferably used.

Examples of silicone resins having no amino group include known epoxy-modified, carboxyl-modified, carbinol-modified, alcohol-modified, phenol-modified, (meth) acryl-modified, mercapto-modified reactive silicones; polyether-modified, methylstyryl-modified, Non-reactive silicones such as alkyl-modified, alkyl-aralkyl-modified, fatty acid-modified, alkoxy-modified, and fluorine-modified; straight silicones such as dimethyl silicone, methylphenyl silicone, diphenyl silicone, and methylhydrogen silicone. One or more can be appropriately selected from these. The silicone resin is used in an amount of 0.1 to 5% by weight in the printing ink 2 containing the polyamide-based and cellulose-based resins. Within the above range, the effect of improving the blocking resistance and the smoothness with the printed layer 1 on the side of the article substrate is preferable. In addition, it floats on the surface of the coating film in an oily state, preventing slime and design deterioration.

As the surfactant, anionic, nonionic, cationic, amphoteric surfactants can be used. The surfactant is 0.05% by weight or more in the printing ink 2 from the viewpoint of blocking resistance with the printing layer 1 on the side that becomes the surface of the substrate of the article and smoothness, and floats on the surface of the coating film in an oily state. From the viewpoints of slime and design, it is preferably contained in the printing ink 2 at 5% by weight or less. Furthermore, it is more preferable that it is contained in the range of 0.1 to 2% by weight.

In the printing ink 2 used in the present invention, a titanium chelate can be used as a cohesion improver.

The titanium chelate has a Ti—O—C type bond in one molecule, and specific examples thereof include titanium chelates such as titanium alkoxide and titanium acylate.

Typical examples of the titanium chelate include titanium alkoxides such as tetraisopropyl titanate, tetranormal butyl titanate, butyl titanate dimer, tetra (2-ethylhexyl) titanate, tetramethyl titanate, tetrastearyl titanate, triethanolamine titanate, titanium acetyl acetate, Mention may be made of titanium chelates such as titanium ethyl acetoacetate, titanium lactate, octylene glycol titanate, titanium tetraacetylacetonate. Among these, chelate-type titanium organic compounds generally require heating to complete the crosslinking reaction, but are hardly hydrolyzed at room temperature and have excellent stability and are suitable for use in inks. In particular, those having an amine in the molecule can be preferably used.

Titanium chelate is suitable in terms of blocking resistance and friction resistance because it has an alkoxy group in one molecule and contributes to the intermolecular or intramolecular crosslinking of the resin.

The printing ink 2 can be used in combination with an isocyanate curing agent depending on the application, base material, and necessary physical properties. As an example of the isocyanate curing agent to be used, diisocyanate includes hexamethylene diisocyanate (HDI), isophorone diisocyanate (IPDI), and xylylene diisocyanate (XDI). Examples of the modified polyisocyanate include adduct type, bifunctional prepolymer type, and biuret type. From the viewpoint of inhibiting heat shrinkage of the heat-shrinkable film, it is desirable that the diisocyanate is selected from HDI and IPDI, and the modified polyisocyanate is selected from an adduct type and a bifunctional prepolymer. These curing agents can be used alone or in admixture of two or more, and preferably 1 to 10% by weight in 100 parts by weight of the printing ink 2. When the content is within the above range, drying in the printed matter becomes good, and thus blocking resistance can be secured. Further, the design printed layer is cured to have an appropriate hardness, and sufficient followability can be secured in the heat shrinkage of the heat shrinkable film.

The printing ink 1 and the printing ink 2 can be produced by using a pigment, a dispersant, a resin other than the resin, and the like, if necessary, and dissolving or dispersing the colorant in the solvent by a known method. . Preferably, a pigment dispersion is produced using a colorant and a resin, and if necessary, a dispersant, and the resin and necessary additives are further mixed and stirred.

For the printing ink 1 and the printing ink 2, known inorganic pigments and organic pigments can be used.

Examples of inorganic pigments include titanium oxide, zinc oxide, zinc sulfide, barium sulfate, calcium carbonate, chromium oxide, and silica. Titanium oxide is preferably used for the white ink pigment from the viewpoint of coloring power, hiding power, chemical resistance, and weather resistance.

Examples of inorganic pigments other than white pigments include carbon black, aluminum, mica (mica) and the like. Aluminum is in the form of powder or paste, but is preferably used in the form of paste from the viewpoint of handling and safety, and whether to use leafing or non-leafing is appropriately selected from the viewpoint of brightness and concentration.

Organic pigments include azo, phthalocyanine, anthraquinone, perylene, perinone, quinacridone, thioindigo, dioxazine, isoindolinone, quinophthalone, azomethine azo, dictopyrrolopyrrole, isoindoline, etc. Pigments. Indigo ink is copper phthalocyanine, and transparent yellow ink is C.I. I. Pigment No Yellow 83 is preferably used.

It is preferable that the pigment is contained in an amount sufficient to ensure the concentration and coloring power of the printing ink 1 and the printing ink 2, that is, 1 to 50% by weight with respect to the total weight of the printing ink. These pigments can be used alone or in combination of two or more.

As the dispersant, anionic, nonionic, cationic, amphoteric surfactants can be used. The dispersant is preferably contained in the ink in an amount of 0.05% by weight or more based on the total weight of the ink from the viewpoint of the storage stability of the ink and 5% by weight or less from the viewpoint of the suitability for lamination. Furthermore, it is more preferable that it is contained in the range of 0.1 to 2% by weight.

Examples of the solvent used for the printing ink 1 and the printing ink 2 include the solvents described in the resin used for the printing ink 1 and the printing ink 2.

In the printing ink 1 and the printing ink 2, the dilution solvent used at the time of printing is to adjust the viscosity and control the printing effect, the density of the printed material, etc. It can select suitably from the solvent used for the printing ink 1 and the printing ink 2. FIG.

The printing ink 1 and the printing ink 2 can be used in combination with various resins depending on the application and the substrate. Examples of the resin used include chlorinated polypropylene resin, vinyl acetate resin, polyester resin, alkyd resin, polyvinyl chloride resin, rosin resin, terpene resin, phenol-modified terpene resin, ketone resin, cyclized rubber, chlorinated rubber, Examples include butyral, petroleum resin, and modified resins thereof. These resins can be used alone or in combination of two or more, and the content thereof is preferably 5 to 25% by weight based on the total weight of the ink.

For the pigment dispersion, known roller mills, ball mills, pebble mills, attritors, sand mills and the like can be used.

The ink viscosity produced by the above method is in the range of 10 mPa · s or more from the viewpoint of preventing the pigment from settling and being appropriately dispersed, and 1000 mPa · s or less from the viewpoint of workability efficiency during ink production or printing. preferable. In addition, the said viscosity is a viscosity measured at 25 degreeC with the Tokimec B-type viscometer.

The printing layer printed using the printing ink 1 and the printing ink 2 has a thickness of 0.5 to 10 μm, and is formed on the entire surface or a part of the article and the synthetic resin film depending on the application.

The packaging body manufacturing method of the present invention can manufacture a packaging body by wrapping all or part of an article with an exterior body. That is, when a heat-shrinkable synthetic resin film is used as the exterior body, it is preferable to have a step of wrapping an article and then shrinking the heat-shrinkable synthetic resin film by heating.

Although various methods can be considered as a method of attaching the exterior body to the article depending on the shape and application of the article, the following can be exemplified as typical methods.
1) A method in which the outer body is molded into a bag shape that has been opened only on one side, and then encased in an article.
2) Forming the exterior body into a cylindrical shape in advance and enclosing it in an article
3) A method of wrapping the outer casing around the outer periphery of the article along the outer periphery, and wrapping both ends of the outer casing in an overlapping manner. Thereafter, the opening of the outer casing is opened so that the article does not come out of the outer casing. It is preferable to heat-seal and heat-seal the synthetic resin film to close the mouth.

A package can be manufactured by wrapping all or part of the article by other known methods.

EXAMPLES Hereinafter, although an Example is given and this invention is demonstrated in detail, this invention is not limited to these Examples. In the present invention, “parts” and “%” represent “parts by weight” and “% by weight” unless otherwise noted.

<Method of measuring amine value>
Weigh 0.5-2 g of sample accurately. (Sample amount: Sg) 30 mL of neutral ethanol (BDG neutral) is added to a precisely weighed sample and dissolved. The obtained solution is titrated with a 0.2 mol / l ethanolic hydrochloric acid solution (titer: f). The point at which the color of the solution changed from green to yellow was taken as the end point, and the amine value was determined by the following (Formula 1) using the titration amount (AmL) at this time.
(Formula 1) Amine number = (A × f × 0.2 × 56.108) / S

<Number average molecular weight (Mn), weight average molecular weight (Mw)>
The number average molecular weight (Mn) and the weight average molecular weight (Mw) were measured using Showa Denko GPC (gel permeation chromatography) “Shodex GPC System-21”. GPC is liquid chromatography that separates and quantifies substances dissolved in a solvent based on the difference in molecular size. Tetrohydrofuran is used as a solvent, and weight average molecular weight (Mn) is determined in terms of polystyrene.

<Hydroxyl value (OHV)>
About 1 g of a sample is accurately weighed in a stoppered Erlenmeyer flask and dissolved by adding 100 ml of a toluene / ethanol (volume ratio: toluene / ethanol = 2/1) mixed solution. Further, exactly 5 ml of an acetylating agent (a solution in which 25 g of acetic anhydride was dissolved in pyridine to make a volume of 100 ml) was added and stirred for about 1 hour. To this, phenolphthalein reagent is added as an indicator and lasts for 30 seconds. Thereafter, the solution is titrated with a 0.1N alcoholic potassium hydroxide solution until the solution becomes light red.
The hydroxyl value was determined by (Formula 2). The hydroxyl value was a numerical value in the dry state of the resin (unit: mgKOH / g).
(Formula 2) Hydroxyl value (mgKOH / g) = [{(ba) × F × 28.25} / S] / (Nonvolatile content concentration / 100) + D
Where S: Amount of sample collected (g)
a: Consumption of 0.1N alcoholic potassium hydroxide solution (ml)
b: Consumption of 0.1N alcoholic potassium hydroxide solution in the empty experiment (ml)
F: Potency of 0.1N alcoholic potassium hydroxide solution
D: Acid value (mgKOH / g)

<Acid value (AV)>
About 1 g of sample compound (B) was accurately weighed in a stoppered Erlenmeyer flask, and dissolved by adding 100 ml of a toluene / ethanol (volume ratio: toluene / ethanol = 2/1) mixed solution. To this was added a phenolphthalein test solution as an indicator, which was held for 30 seconds, and then titrated with a 0.1N alcoholic potassium hydroxide solution until the solution turned light red.
The acid value (mgKOH / g) was determined by (Equation 3) as the value of the resin in the dry state.
(Formula 3) Acid value (mgKOH / g) = {(5.611 × a × F) / S} / (Nonvolatile content concentration / 100)
Where S: Amount of sample collected (g)
a: Consumption of 0.1N alcoholic potassium hydroxide solution (ml)
F: Potency of 0.1N alcoholic potassium hydroxide solution

<Example of production of printing ink 1>
(Synthesis example of polyester diol)
In a round bottom flask equipped with a stirrer, a thermometer, a water separator and a nitrogen gas introduction tube, 56.846 parts of 2-butyl-2-ethyl-1,3-propanediol (hereinafter abbreviated as BEPG) and 43. adipic acid. 152 parts and 0.002 part of tetrabutyl titanate were charged, and esterification was carried out for 8 hours while removing water produced by condensation at 230 ° C. under a nitrogen stream. After confirming that the acid value of the polyester was 15 or less, the degree of vacuum was gradually raised with a vacuum pump to complete the reaction. As a result, a polyester diol having a hydroxyl value of 56.1 mgKOH / g (number average molecular weight 2000 calculated from the hydroxyl value) and an acid value of 0.3 mgKOH / g was obtained.

(Synthesis example of urethane resin 1)
A four-necked flask equipped with a stirrer, a thermometer, a reflux condenser and a nitrogen gas inlet tube is charged with 22.226 parts of the polyester diol, 5.434 parts of isophorone diisocyanate, and 7.500 parts of ethyl acetate. The mixture was reacted at 120 ° C. for 6 hours under a stream of air, and 7.500 parts of ethyl acetate was added and cooled to obtain 42.663 parts of a solution of a terminal isocyanate prepolymer. Next, 42.663 parts of the solvent solution of the obtained terminal isocyanate prepolymer was added to a mixture of 2.203 parts of isophoronediamine, 0.138 parts of di-n-butylamine, 20.000 parts of ethyl acetate and 20.000 parts of ethanol. Gradually add at room temperature, then react at 50 ° C. for 1 hour, add 15.000 parts ethanol, urethane resin with solid content 30.0%, weight average molecular weight 24000, amine number 4.0 mg KOH / resin 1 g 1 was obtained.

(Synthesis example of urethane resin 2)
In the same manner as in the synthesis example of urethane-based resin 1, 22.226 parts of the above-mentioned polyester diol, 5.434 parts of isophorone diisocyanate, and 7.500 parts of ethyl acetate were charged and reacted at 120 ° C. for 6 hours under a nitrogen stream. 7.500 parts of ethyl acetate was added and cooled to obtain 42.663 parts of a solution of a terminal isocyanate prepolymer. Next, 42.663 parts of a solvent solution of the resulting terminal isocyanate prepolymer was added to a mixture of 4.406 parts of isophoronediamine, 0.138 parts of di-n-butylamine, 20.000 parts of ethyl acetate and 20.000 parts of ethanol. Gradually add at room temperature, then react at 50 ° C. for 1 hour, add 15.000 parts ethanol, urethane resin with solid content 30.0%, weight average molecular weight 24000, amine number 8.0 mg KOH / resin 1 g 2 was obtained.

(Synthesis example of urethane resin 3)
In the same manner as in the synthesis example of urethane-based resin 1, 22.226 parts of the above-mentioned polyester diol, 5.434 parts of isophorone diisocyanate, and 7.500 parts of ethyl acetate were charged and reacted at 120 ° C. for 6 hours under a nitrogen stream. 7.500 parts of ethyl acetate was added and cooled to obtain 42.663 parts of a solution of a terminal isocyanate prepolymer. Next, 42.663 parts of the solvent solution of the obtained terminal isocyanate prepolymer was added to a mixture of 8.812 parts of isophoronediamine, 0.138 parts of di-n-butylamine, 20.000 parts of ethyl acetate and 20.000 parts of ethanol. Slowly add at room temperature, then react at 50 ° C. for 1 hour, add 15.000 parts ethanol, urethane resin with solid content 30.0%, weight average molecular weight 24000, amine value 13.0 mg KOH / resin 1 g 2 was obtained.

(Adjustment of cellulose resin)
20 parts of nitrocellulose resin [Inabata Sangyo Co., Ltd., Standard L1 / 2, trade name DLX30-50] is dissolved in a mixed solvent in which isopropyl alcohol and ethyl acetate are mixed in equal amounts, and the nitrocellulose resin has a solid content of 20%. A varnish was obtained.

(Synthesis example of acrylic resin)
As acrylic monomers, 37 parts of methyl methacrylate [glass transition temperature Tg = + 105 ° C. of homopolymer] and 60 parts of butyl methacrylate [glass transition temperature Tg = + 20 ° C. of homopolymer], acrylic acid [of homopolymer Glass transition temperature Tg = + 106 ° C.] The copolymer was copolymerized so as to have a composition ratio of 3 parts to prepare an acrylic resin having a weight average molecular weight of 50000 and Tg of 50 ° C. The prepared acrylic resin was dissolved in a mixed solvent in which isopropyl alcohol and ethyl acetate were mixed in equal amounts to prepare an acrylic resin having an acrylic resin solid content of 40%.

(Ink 1)
After 25.0 parts of pigment titanics JR-805 (manufactured by Teika), 15.0 parts of urethane-based resin 1, 5.0 parts of ethyl acetate, 5.0 parts of ethanol, and kneaded in a sand mill, 10.0 parts of urethane resin 1, 20.0 parts of ethyl acetate, and 20.0 parts of ethanol were stirred and mixed to obtain a white diluted printing ink (ink 1).

(Ink 2-5)
Each raw material was changed as described in Table 1, and inks 2 to 5 were obtained in the same manner as ink 1.

In the present specification, inks 6 to 13, 18, 20 to 23 are reference examples.
<Example of production of printing ink 2>
(Vinyl chloride / vinyl acetate copolymer resin 1)
Solvain TAO (manufactured by Shin-Etsu Chemical Co., Ltd.), softening point 78 ° C., number average molecular weight 15,000, monomer ratio of vinyl chloride: vinyl acetate: vinyl alcohol is 91: 2: 7
(Vinyl chloride / vinyl acetate copolymer resin 2)
VINNOL E15 / 45 (manufactured by Shin-Etsu Chemical Co., Ltd.), softening point 75 ° C., number average molecular weight 13,000, monomer ratio of vinyl chloride: vinyl acetate: vinyl alcohol is 85: 15: 0
(Acid-modified rosin resin 1)
· Harimac 4740 (manufactured by Harima Chemicals), softening point 115-125 ° C, acid value 15-30
(Acid-modified rosin resin 2)
・ Marquide 3002 (manufactured by Arakawa Chemical Co., Ltd.), softening point 165 to 185 ° C., acid value 90 to 110
(Acid-modified rosin resin 3)
-Harimac T-80 (manufactured by Harima Chemicals), softening point 80-90 ° C, acid value 170-200

(Ink 6)
Pigment RAVEN 1020 (Columbian) 15.0 parts, vinyl chloride / vinyl acetate copolymer resin 1 6.0 parts, urethane resin 1 5.0 parts, ethyl acetate 5.0 parts, ethanol 5. After stirring and mixing with 0 parts and kneading with a sand mill, 14.0 parts of urethane resin 1, 25.0 parts of ethyl acetate, and 25.0 parts of ethanol were stirred and mixed to obtain a black diluted printing ink (ink 6).

Silicon oil, Shin-Etsu silicon KP-355 (manufactured by Shin-Etsu Silicone Co., Ltd.)

Surfactant / Plysurf A208-15N (Daiichi Kogyo Seiyaku Co., Ltd.)

(Ink 7-25)
Each raw material was changed as described in Table 2, and inks 7 to 25 were obtained in the same manner as ink 6. The inks 21 to 25 having no pigment are only stirred and mixed.

(Ink 26-37)
Each raw material was changed as described in Table 3, and inks 26 to 37 were obtained in the same manner as ink 6. The inks 33 to 37 having no pigment are only stirred and mixed.

In this specification, the packaging bodies of Examples 1 to 8, 17, and 19 to 22 are reference examples.
[Example 1]
<Method for creating article 1>
Under the following printing conditions, the ink 1 was printed on the treated surface of a PET film E5100-100μ (manufactured by Toyobo Co., Ltd.) as a base material of the article to obtain an article 1.

[Printing conditions]
Printing machine: Gravure printing machine manufactured by Fuji Kikai Kogyo Co., Ltd. Impression cylinder: NBR (nitrile butadiene rubber) doctor with rubber hardness of 80Hs: Ceramic plated doctor blade with blade thickness of 60 μm (base material thickness 40 μm, thickness of one side ceramic layer) 10μm)
Plate: Toyo Prepress Co., Ltd., chrome hardness 1050Hv electronic engraving plate (stylus angle 130 degrees, for printing ink: 175 lines / inch, for thermal adhesive: 100 lines / inch)
Printing pressure: 2kg / cm ²
Doctor pressure: 2kg / cm ²
Printing speed: 60 m / min Drying temperature: F100 ° C

<Method for creating exterior body 1>
Under the same conditions, ink 6 was printed on the treated surface of the OPP film FOH-30μ (manufactured by Futamura Chemical Co., Ltd.), which is a synthetic resin film, to obtain the outer package 1.

<Method for creating package 1>
Two pieces of the obtained exterior body 1 are cut out at 7.5 cm × 10.5 cm, and the respective printing surfaces are inside, and the three edges are thermally bonded by a single-acting heat sealer having a width of 1 cm under the following conditions. Only made an opened bag. Thereafter, the article 1 was cut out at 5 cm × 8 cm, put into the above-mentioned bag, the opening part was thermally bonded with a single-acting heat sealer, and the package 1 was obtained by closing.
Thermal bonding conditions Thermal bonding temperature: 130 ° C
Thermal bonding condition: 1.0 second Thermal bonding pressure: 2 kg / cm ²

[Examples 2 to 24]
<Method for creating articles 2-5>
As described in Table 4, the inks 2 to 5 were respectively printed on PET film E5100-100μ (manufactured by Toyobo Co., Ltd.) or coated paper (Reuo coated paper (manufactured by Daio Paper Co., Ltd.)), and articles 2-5 Got. The printing conditions are the same as in Example 1.

<Creating method of exterior bodies 2-24>
As described in Table 4, in the same manner as the method for producing the outer package 1, ink 7 to 25 was printed on the treated surface of the OPP film FOH-30μ (Futamura Chemical Co., Ltd.). Obtained.

<Method for creating packaging 2-24>
As described in Table 4, the articles 1 to 5 and the outer packaging bodies 2 to 24 were laminated in the same manner as in the method for producing the packaging body 1 to obtain Examples 2 to 24 (packaging bodies 2 to 24).

[Comparative Examples 1 to 12]
<Method of creating exterior bodies 25-36>
As described in Table 4, the inks 26 to 37 were printed on the treated surface of the OPP film FOH-30μ (manufactured by Phutamura Chemical Co., Ltd.) in the same manner as in the method for producing the outer package 1, and the outer packages 25 to 36 were obtained. Obtained.

<Method for creating packaging bodies 25-36>
As described in Table 4, the article 1 and the outer packaging bodies 25 to 36 were laminated in the same manner as in the method for producing the packaging body 1 to obtain Comparative Examples 1 to 12 (packaging bodies 25 to 36).

The description of Table 4 is as follows.
○: The corresponding base material is used, and ink is printed and laminated.
Blank or “None”: The corresponding substrate or ink is not used.
Taking Example 1 as an example, an article in which an ink 1 is laminated on a PET film and an exterior body in which an ink 6 is laminated on an OPP film are separately created, and a package is created using them. Used in the following test.

Example 20 will be described as an example. An article in which ink 1 is laminated on a PET film and an exterior body in which ink 10 and ink 21 are laminated in sequence on an OPP film are separately prepared and packaged using these. Was used for the following test.

<Abrasion resistance test between printed layers of article and exterior>
About the article and exterior body of the obtained packaging body, the respective printed layers are overlapped with a Gakushin type anti-friction tester and rubbed 100 times with a load of 0.5 kg / cm ² , and then the article and the exterior body. Friction resistance was evaluated from the degree of ink peeling.

◎: The ink was not peeled off at all ○: The ink peeled area was 0-20% △: The ink peeled area was 20-50% (practical level or more)
X: The area where the ink peeled was 50 to 75%

<Blocking resistance test between printed layers of article and exterior body>
For the packaged article and the outer package obtained, the printed layers of the respective printed materials cut to the same size were overlapped, a load of 1.0 kg / cm ² was applied, and the atmosphere was 50 ° C. and 80% RH. After standing for a period of time, the printed layers of the article and the outer package were peeled off, and blocking resistance was evaluated from the degree of ink peeling.

A: The ink is not peeled. B: The area where the ink is peeled is 0 to 20%. Δ: The area where the ink is peeled is 20 to 50% (practical level or more).
X: The area where the ink peeled was 50 to 75%

<Tape adhesion test>
About the outer package of the obtained package, a cellophane tape is pressure-bonded to the printed surface, and then the peeled state of the printed surface when the tape is peeled off is observed.

A: The ink is not peeled. B: The area where the ink is peeled is 0 to 20%. Δ: The area where the ink is peeled is 20 to 50% (practical level or more).
X: The area where the ink peeled was 50 to 75%

<Heat-resistant blocking test between printed layers of article and exterior body>
About the article and exterior body of the obtained package, the ink is peeled off immediately after being punched into a 25 mm x 60 mm strip, and the printed layers are combined and thermally bonded under the following conditions using a single-acting heat sealer. The heat-resistant blocking property was evaluated from the degree of.
Thermal bonding conditions Thermal bonding temperature: 130 ° C
Thermal bonding condition: 1.0 second Thermal bonding pressure: 2 kg / cm ²

A: The ink is not peeled. B: The area where the ink is peeled is 0 to 20%. Δ: The area where the ink is peeled is 20 to 50% (practical level or more).
X: The area where the ink peeled was 50 to 75%

Packaging body having printing layer 2 containing urethane-based resin and vinyl chloride / vinyl acetate copolymer-based resin and / or acid-modified rosin-based resin on the back surface side of the exterior body shown in Examples 1-24 Was excellent in the friction resistance, blocking resistance and heat blocking resistance between the printed surfaces of the article and the exterior body, and the tape adhesiveness of the exterior body also had physical properties exceeding the practical level. On the other hand, Comparative Examples 1 to 12 are required in a package formed by packaging an article with an exterior body, and the tape adhesion of the exterior body and the friction resistance between the printed surfaces of the article and the exterior body, It was confirmed that the physical properties of either blocking resistance or heat blocking resistance were inferior, and a practical level could not be achieved.

Claims (4)

A package having an article and an exterior body on the outside thereof, the package having the following (1) to ( 3 ).
(1) The article has the printing layer 1 on a part or the entire surface of the substrate , the exterior body has the printing layer 2 on the synthetic resin film, and the printing layer 2 is in contact with at least the printing layer 1. It is arranged on the surface.
(2) The printing layer 1 contains one or more resins selected from acrylic resins, cellulose resins, and urethane resins.
(3) printed layer 2, and a urethane-based resin, a vinyl chloride / vinyl acetate copolymer resin, containing from 40.7 to 100 wt% in total and acid-modified rosin resin, and the urethane resin, chloride The solid content weight ratio of the vinyl / vinyl acetate copolymer resin and the acid-modified rosin resin is 65:35 to 35:65 .   2. A package according to claim 1, wherein the base material of the article is paper. Package of claim 1 or 2, wherein the exterior body is one that is heat-shrinkable. The package according to any one of claims 1 to 3, wherein the printed layer 2 contains a surfactant and / or silicon oil.

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