JP2022104525A - Base paper for metallized paper, and metallized paper - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide base paper for metallized paper capable of providing metallized paper having excellent barrier properties.

SOLUTION: The base paper for metallized paper has, on at least one face of a paper base material, a clay coat layer and a resin layer in this order, where the resin layer surface has a wet tension of 50 mN/m or more as measured according to JIS K 6768:1999, and a print-surf surface roughness of 2.5 μm or less as measured in accordance with JIS P 8151:2004.

SELECTED DRAWING: None

COPYRIGHT: (C)2022,JPO&INPIT

Description

The present invention relates to a base paper for vapor-deposited paper and a vapor-deposited paper using the same.

Conventionally, packaging materials that have a water vapor barrier property that barriers water vapor and a gas barrier property that barriers gases other than water vapor, in particular, an oxygen barrier property that barriers oxygen, have been used for foods, medical products, electronic parts, etc. It is used in packaging to prevent deterioration of the quality of the contents.

The thin-film vapor deposition paper is made by providing a thin-film deposition layer made of metal or the like on a paper base material, and by taking advantage of its glossiness, it is a label paper with excellent design such as liquor and refreshing drinking water, and a wrapping paper for confectionery. It is widely used for such purposes.

For example, in Patent Document 1, in an aluminum-deposited paper in which an aluminum-deposited layer is provided on a base paper, the back surface of the aluminum-deposited layer is treated so that the natural polarization potential value of the surface of the vapor-deposited layer is within a specific range. The paper is disclosed. Further, for example, in Patent Document 2, a sealing coating layer with a polyolefin-based aqueous dispersion liquid, a thin-film film layer of an inorganic oxide, and a heat-sealing resin layer are provided on one side of a thin paper having a basis weight of a specific value or less. The sequentially formed sealing sheets for PTP packaging are disclosed.

Japanese Unexamined Patent Publication No. 4-65599 Japanese Unexamined Patent Publication No. 7-223686

Although attempts have been made to improve the barrier property of the paper substrate against oxygen and water vapor by forming a thin-film deposition layer as in Patent Documents 1 and 2, the aluminum-deposited paper and Patent Document 2 described in Patent Document 1 have been made. The sealed sheet for PTP packaging described in the above has a problem of poor gas barrier property.

The vapor-deposited paper used as a food packaging material is required to have further improved barrier properties (oxygen barrier property, water vapor barrier property) from the viewpoint of protecting the flavor of food. Therefore, an object of the present invention is to provide a base paper for thin-film deposition paper which can provide a thin-film deposition paper having excellent barrier properties.

The present inventors have found that the above problems can be solved by adjusting the surface characteristics and the like of the base paper for vapor-deposited paper, and have completed the present invention.

That is, the present invention relates to the following <1> to <15>.
<1> A base paper for vapor-deposited paper having a clay coat layer and a resin layer on at least one surface of a paper base material in this order, and the surface of the resin layer has a wet tension measured in accordance with JIS K 6768: 1999. Is 50 mN / m or more, and the print surf surface roughness measured in accordance with JIS P 8151: 2004 is 2.5 μm or less.
<2> The base paper for vapor-deposited paper according to <1>, wherein the resin layer contains a resin having a glass transition temperature of 50 ° C. or higher.
<3> The base paper for vapor-deposited paper according to <1> or <2>, wherein the resin layer contains a water-suspendable polymer.
<4> The vapor deposition according to any one of <1> to <3>, wherein the water-suspendable polymer contained in the resin layer is at least one selected from the group consisting of polyester-based resin and polyurethane-based resin. Base paper for paper.
<5> The polyurethane resin has an oxygen permeability of 100 mL / (m ² · day · atm) or less at 23 ° C. and 50% RH when converted into a sheet having a thickness of 25 μm, according to <4>. Base paper for vapor-deposited paper.
<6> The polyurethane-based resin contains at least one selected from the group consisting of a structural unit derived from metaxylylene diisocyanate and a structural unit derived from hydrogenated metaxylylene diisocyanate, according to <4> or <5>. The described base paper for vapor-deposited paper.
<7> The polyurethane resin has a total content of the constituent units derived from metaxylylene diisocyanate and the constituent units derived from hydrogenated metaxylylene diisocyanate of 50 mol% or more with respect to the total amount of the constituent units derived from polyisocyanate. The base paper for vaporized paper according to any one of <4> to <6>.
<8> The clay coat layer contains an inorganic pigment and a binder, and the inorganic pigment has an aspect ratio of 50 or less and an average particle diameter of 5 μm or less, according to any one of <1> to <7>. Base paper for vapor-deposited paper.
<9> The base paper for thin-film deposition paper according to <8>, wherein the inorganic pigment is kaolin.
<10> The binder contained in the clay coat layer is one or more selected from the group consisting of styrene-butadiene resin, styrene- (meth) acrylic resin, olefin-unsaturated carboxylic acid copolymer, and polylactic acid. The base paper for vaporized paper according to <8> or <9>.
<11> The base paper for vapor-deposited paper according to any one of <1> to <10>, wherein the clay coat layer and the resin layer are formed by using an aqueous medium.
<12> A vapor-deposited paper having a vapor-deposited layer on the resin layer of the base paper for vapor-deposited paper according to any one of <1> to <11>.
<13> A polyurethane-based resin containing an overcoat layer is provided on the thin-film deposition layer, and the polyurethane-based resin contained in the overcoat layer is a structural unit derived from metaxylylene diisocyanate and a configuration derived from hydrogenated metaxylylene diisocyanate. The vapor-deposited paper according to <12>, which contains at least one selected from the group consisting of units.
<14> A heat-sealing layer containing a thermoplastic resin is provided on the overcoat layer, and the heat-sealing layers are heat-sealed at 160 ° C., 0.2 MPa, and 1 second, and the test piece has a width of 15 mm. The vapor-deposited paper according to <13>, wherein the maximum load heat seal peeling strength when T-shaped peeling is performed at a tensile speed of 300 mm / min is 2N / 15 mm or more.
<15> Oxygen permeability at 23 ° C. and 50% RH is 1.0 mL / (m ²・ day ・ atm) or less, and water vapor permeability at 40 ° C. and 90% RH is 1.0 g / (m ² ). The vapor-deposited paper according to any one of <12> to <14>, which is less than or equal to day).

INDUSTRIAL APPLICABILITY According to the present invention, it is possible to provide a base paper for thin-film deposition paper which can provide a thin-film deposition paper having excellent barrier properties.

The base paper for vapor-deposited paper of the present embodiment has a clay coat layer and a resin layer on at least one surface of a paper base material in this order, and the surface of the resin layer is wetted according to JIS K 6768: 1999. The tension is 50 mN / m or more, and the print surf surface roughness measured according to JIS P 8151: 2004 is 2.5 μm or less. The thin-film vapor-deposited paper produced by using the base paper for thin-film vapor-deposited paper of the present embodiment has excellent barrier properties (oxygen barrier property, water vapor barrier property). The mechanism that exerts this effect is unknown, but it is presumed as follows.

By setting the wetting tension on the surface of the resin layer to 50 mN / m or more, the polarity of the surface of the resin layer is increased, and the adhesion between the resin layer and the thin-film deposition layer formed on the layer is improved. Further, by setting the print surf surface roughness of the resin layer surface to 2.5 μm or less, a thin-film deposition layer having few defects can be formed on the resin layer. For these reasons, the thin-film vapor-deposited paper produced by using the base paper for thin-film vapor-deposited paper of the present embodiment can exhibit excellent barrier properties. It should be noted that the above mechanism is speculative, and the mechanism for achieving the effect of the present invention is not limited thereto.

Hereinafter, the structure and physical properties of the water-resistant paper of the present embodiment will be described in more detail. In the present specification, the numerical range represented by "X to Y" means a numerical range including X as a lower limit value and Y as an upper limit value. Further, "(meth) acrylic" is a general term including both acrylic and methacrylic acid.

The base paper for vapor-deposited paper of the present embodiment may have a clay coat layer and a resin layer on one side of a paper base material in this order, or may have a clay coat layer and a resin layer on both sides in this order. However, from the viewpoint of production efficiency, it is preferable to have a clay coat layer and a resin layer on one side in this order.

<Paper base material>
The pulp constituting the paper base material in the present embodiment preferably contains plant-derived pulp as a main component, and more preferably wood pulp as a main component. Examples of wood pulp include hardwood pulp and softwood pulp. Examples of non-wood pulp include cotton pulp, hemp pulp, kenaf pulp, bamboo pulp and the like. Materials other than pulp fibers such as synthetic fibers such as rayon fibers and nylon fibers may also be blended as auxiliary paper materials as long as the effects of the present invention are not impaired.

The ratio of hardwood pulp to the pulp constituting the paper base material is preferably 65% by mass or more, more preferably 80% by mass or more, still more preferably 90% by mass or more, still more preferably 95% by mass or more. , 100% by mass. When the ratio of pulp hardwood pulp constituting the paper base material is within the above range, the recyclability is excellent.

Specific examples of the paper base material used for the base paper for vapor-deposited paper of the present embodiment include bleached kraft paper, unbleached kraft paper, high-quality paper, paperboard, liner paper, coated paper, single-gloss paper, and glassin paper. Examples include graphan paper. Among these, bleached kraft paper, unbleached kraft paper, woodfree paper, and single glossy paper are preferable.

(Degree of size)
The degree of size of the paper substrate is not particularly limited, but from the viewpoint of improving the barrier property, it is preferable that the degree of sizing human size according to JIS P 8122: 2004 is 1 second or more. The upper limit is not particularly limited, but is preferably 100 seconds or less, more preferably 30 seconds or less. The degree of size of the paper substrate can be controlled by the type and content of the internal sizing agent, the type of pulp, the smoothing treatment, and the like.

Examples of the internal sizing agent include rosin type, alkyl ketene dimer type, alkenyl succinic anhydride type, styrene-unsaturated carboxylic acid type, higher fatty acid type, petroleum resin type and the like. The content of the internal sizing agent is not particularly limited, but is preferably 0 parts by mass or more and preferably 3 parts by mass or less with respect to 100 parts by mass of the pulp of the paper base material.

In addition to the internal sizing agent, other known internal additives may be added to the paper substrate. Examples of the internal additive include a filler, a paper strength enhancer, a yield improver, a pH adjuster, a drainage improver, a water resistant agent, a softener, an antistatic agent, an antifoaming agent, a slime control agent, a dye, and a pigment. And so on.

Examples of the filler include titanium dioxide, kaolin, talc, calcium carbonate (heavy calcium carbonate, light calcium carbonate), calcium sulfite, gypsum, calcined kaolin, white carbon, amorphous silica, delaminated kaolin, diatomaceous soil, and carbonic acid. Examples thereof include magnesium, aluminum hydroxide, calcium hydroxide, magnesium hydroxide and zinc hydroxide.

The paper substrate is obtained by making a papermaking material containing a pulp slurry as a main component.

The pulp slurry is obtained from wood or non-wood raw material chips through steps such as cooking, washing and bleaching. The method in the cooking step, the washing step, the bleaching step and the like is not particularly limited. The pulp slurry obtained through these steps is further beaten in the presence of water.

For paper making of a paper base material, a known wet paper machine can be appropriately selected and used. Examples of the paper machine include a long net type paper machine, a gap former type paper machine, a circular net type paper machine, and a short net type paper machine. It is preferable that the paper layer formed by the paper machine is conveyed by, for example, felt and dried by a dryer. A multi-stage cylinder dryer may be used as a pre-dryer before drying the dryer.

Further, the paper substrate obtained as described above may be surface-treated with a calendar to make the paper thickness and gloss profile uniform. As the calendar processing, a known calendar processing machine can be appropriately selected and used.

(Basis weight)
The basis weight of the paper substrate is not particularly limited, but is preferably 20 g / m ² or more, more preferably 30 g / m ² or more, further preferably 40 g / m ² or more, and. It is preferably 500 g / m ² or less, more preferably 400 g / m ² or less, further preferably 200 g / m ² or less, and even more preferably 100 g / m ² or less. The basis weight of the paper substrate is measured in accordance with JIS P 8124: 2011.

(thickness)
The thickness of the paper substrate is not particularly limited, but is preferably 5 μm or more, more preferably 10 μm or more, still more preferably 20 μm or more, and preferably 150 μm or less, more preferably 100 μm or less, still more preferably 75 μm or less. Is. The thickness of the paper substrate is measured according to JIS P 8118: 2014.

(density)
From the viewpoint of moldability, the paper substrate preferably has a density of 0.5 g / cm ³ or more, more preferably 0.6 g / cm ³ or more, and 1.2 g / cm ³ or less. It is preferably 1.0 g / cm ³ or less, and more preferably 1.0 g / cm 3. The density of the paper base material is calculated from the basis weight and thickness of the paper base material measured by the above method.

(Oken type smoothness)
From the viewpoint of obtaining a uniform thin-film deposition layer, the paper substrate preferably has a Wangken-type smoothness of at least the surface on which the vapor-film deposition layer is provided, preferably 5 seconds or longer, and more preferably 10 seconds or longer. The upper limit is not particularly limited, but is preferably 1000 seconds or less, for example. The Oken-type smoothness of the paper substrate is measured in accordance with JIS P 8155: 2010.

<Clay court layer>
The base paper for thin-film deposition paper of the present embodiment has a clay coat layer between the paper base material and a resin layer described later. As a result, the paper base material can be sealed and smoothed, and as a result, a flatter resin layer can be formed. ..

The clay coat layer preferably contains an inorganic pigment and a binder, and more preferably mainly composed of an inorganic pigment and a binder. In addition, "the clay coat layer is mainly composed of an inorganic pigment and a binder" means that the total content of the inorganic pigment and the binder in the clay coat layer is, for example, 50% by mass or more, preferably 60% by mass or more. It means that it is preferably 70% by mass or more, more preferably 80% by mass or more, still more preferably 90% by mass or more, and particularly preferably 95% by mass or more. The upper limit is not particularly limited, but is 100% by mass or less. In addition to the inorganic pigment and the binder, the clay coat layer may further contain any component.

(Inorganic pigment)
The inorganic pigment contained in the clay coat layer is not particularly limited, and examples thereof include kaolin, talc, and mica, and kaolin is preferable. The content of the inorganic pigment in the clay coat layer is preferably 50% by mass or more, more preferably 60% by mass or more, further preferably 70% by mass or more, and 98% by mass or less. It is preferably 90% by mass or less, more preferably 85% by mass or less.

≪Aspect ratio≫
The aspect ratio of the inorganic pigment is preferably 50 or less from the viewpoint of forming a uniform and smooth resin layer and from the viewpoint of finely scattering the inorganic pigment in the clay coat layer and improving the dissociation property of the base paper for vapor-deposited paper at the time of recovery. .. The lower limit is not particularly limited, but is preferably 1 or more. The aspect ratio can be measured by observation with an electron microscope or X-ray diffraction measurement.

≪Average particle size≫
The average particle size of the inorganic pigment is preferably 5 μm or less, preferably 3 μm or less, from the viewpoint of forming a uniform and smooth resin layer and finely scattered in the clay coat layer to improve the dissociation property of the base paper for vapor-deposited paper at the time of recovery. The following is more preferable, and 1 μm or less is further preferable. The lower limit is not particularly limited, but is preferably 0.05 μm or more. The average particle size means the median size (d50) measured by the laser diffraction / scattering type particle size distribution measurement.

(binder)
The binder contained in the clay coat layer is not particularly limited, but is limited to styrene-butadiene resin; (meth) acrylic (co) polymer; styrene- (meth) acrylic resin; ethylene-acrylic acid copolymer, ethylene. -Olefin-unsaturated carboxylic acid-based copolymers such as methacrylic acid copolymers; polylactic acid and the like, including styrene-butadiene-based resins, styrene- (meth) acrylic-based resins, and olefin-unsaturated carboxylic acid-based copolymers. , One or more selected from the group consisting of polylactic acid, preferably one or more selected from the group consisting of styrene- (meth) acrylic resin, ethylene- (meth) acrylic acid copolymer, and polylactic acid. More preferably, it is more preferably one or more selected from a styrene-acrylic resin, an ethylene-acrylic acid copolymer, and polylactic acid.

The (meth) acrylic (co) polymer is a (co) polymer of one or more monomers selected from (meth) acrylic acid and (meth) acrylic acid ester. The (meth) acrylic acid ester is not particularly limited, but is preferably an alkyl ester having 1 to 12 carbon atoms of the (meth) acrylic acid.

The styrene- (meth) acrylic resin is a polymer of styrene and at least one monomer selected from (meth) acrylic acid and (meth) acrylic acid ester, and is preferably styrene-acrylic. It is a based resin, more preferably a styrene-acrylic acid copolymer or a styrene-acrylic acid ester copolymer.

The content of the binder in the clay coat layer is preferably 2% by mass or more, more preferably 10% by mass or more, further preferably 15% by mass or more, and 50% by mass or less. It is preferably 40% by mass or less, more preferably 30% by mass or less.

The amount of the clay coat layer applied is not particularly limited, but the solid content is preferably 5 g / m ² or more, more preferably 7 g / m ² or more, and 30 g / m ² or less. It is preferably 20 g / m ² or less, and more preferably 20 g / m 2.

The method for forming the clay coat layer is not particularly limited, but a method of forming the clay coat layer by applying a dispersion liquid containing an inorganic pigment and a resin binder onto a paper substrate and drying it is preferable. As the dispersion liquid containing the inorganic pigment and the resin binder, those using an aqueous medium such as an aqueous dispersion liquid as a solvent are preferable.

<Resin layer>
The base paper for thin-film deposition paper of the present embodiment has a resin layer arranged on the clay coat layer. By providing the resin layer, the adhesion between the vapor-filmed layer of the vapor-filmed paper and the paper substrate is improved, and the barrier property is improved. Further, since the resin layer has an oxygen barrier property and a water vapor barrier property, it also has a function of improving the barrier property when the vapor-deposited paper is used.

The resin layer preferably contains a resin having a glass transition temperature of 50 ° C. or higher. By forming the resin layer using a resin having a glass transition temperature of 50 ° C. or higher, the smoothness of the surface of the resin layer can be maintained even when exposed to high-temperature steam during vapor deposition, and a vapor-deposited layer with few defects can be formed on the resin layer. Can be formed. As a result, it is considered that the obtained vapor-film-deposited paper can exhibit excellent barrier properties. The upper limit of the glass transition temperature of the resin is not particularly limited, but is, for example, 200 ° C. or lower. As will be described later, when the resin contained in the resin layer is a polyester resin or a polyurethane resin, the glass transition temperature is preferable. Is 150 ° C. or lower, more preferably 140 ° C. or lower, still more preferably 135 ° C. or lower. The glass transition temperature of the resin contained in the resin layer can be confirmed by the method described in Examples. That is, a part of the resin layer of the base paper for vapor deposition is carved out, the glass transition temperature is measured according to JIS K 7121: 1987, and if the glass transition temperature is 50 ° C. or higher, the resin layer has a glass transition temperature of 50. It can be said that it contains a resin having a temperature of ℃ or higher. In other words, the resin layer has a glass transition temperature of preferably 50 ° C. or higher as measured in accordance with JIS K 7121: 1987, and the upper limit is not particularly limited, but is, for example, 200 ° C. or lower.

The resin layer preferably contains a water-suspendable polymer, and more preferably mainly contains a water-suspendable polymer. In addition, "the resin layer mainly contains a water-suspendable polymer" means that the content of the water-suspendable polymer in the resin layer is, for example, 50% by mass or more, preferably 60% by mass or more, more preferably. It means that it is 70% by mass or more, more preferably 80% by mass or more, still more preferably 90% by mass or more, and particularly preferably 95% by mass or more. The upper limit is not particularly limited, but is 100% by mass or less. The resin layer may further contain any component in addition to the water-suspendable polymer.

(Water-suspending polymer)
The water-suspendable polymer contained in the resin layer is not particularly limited, but is an alkyd resin; (meth) acrylic (co) polymer, styrene- (meth) acrylic resin; ethylene-acrylic acid copolymer, Olefin-unsaturated carboxylic acid-based copolymers such as ethylene-methacrylic acid copolymer; vinyl alcohol-based resins such as polyvinyl alcohol and ethylene vinyl alcohol copolymers (ethylene-modified polyvinyl alcohol); cellulose-based resins; polyurethane-based resins; Examples include polyester resins. Among these, one or more selected from vinyl alcohol-based resin, polyurethane-based resin and polyester-based resin is preferable, and the polyester-based resin and polyurethane-based resin are used from the viewpoint of further improving the degree of biodegradability and recyclability. It is more preferably one or more selected from the group, and further preferably a polyurethane resin.

≪Polyester resin≫
The polyester-based resin contained in the resin layer is not particularly limited, and for example, it is more preferable that the polyester-based resin can be prepared into one or more selected from the group consisting of polyester-based resin dispersions and emulsions, and polyester-based resin dispersions. It is more preferable that it can be prepared into an emulsion or an emulsion, and even more preferably it can be prepared into a polyester resin dispersion.

As the polyester resin, a commercially available product may be used, and examples thereof include "Elitel KT series (trade name)" manufactured by Unitika Ltd. and "Randy PL series (trade name)" manufactured by Miyoshi Oil & Fat Co., Ltd. Specifically, Elitel KT-8803 and Randy PL-3000 are exemplified.

≪Polyurethane resin≫
The polyurethane-based resin contained in the resin layer is not particularly limited, and for example, it is more preferable that the polyurethane-based resin can be prepared into one or more selected from the group consisting of polyurethane-based resin dispersions and emulsions, and polyurethane-based resin dispersions. It is more preferable that it can be prepared into an emulsion or an emulsion, and even more preferably it can be prepared into a polyurethane resin dispersion.

The polyurethane resin contained in the resin layer preferably contains at least one selected from the group consisting of a structural unit derived from metaxylylene diisocyanate and a structural unit derived from hydrogenated metaxylylene diisocyanate. When the polyurethane resin contains at least one of the constituent units derived from metaxylylene diisocyanate and the constituent units derived from hydrogenated metaxylylene diisocyanate, the constituent units derived from metaxylylene diisocyanate and the constituent units derived from polyisocyanate with respect to the total amount of the constituent units derived from polyisocyanate. The total content of the constituent units derived from the hydrogenated metaxylylene diisocyanate is preferably 50 mol% or more. Such a polyurethane-based resin exhibits a high cohesive force due to hydrogen bonds and a stacking effect between xylylene groups, and thus has excellent gas barrier properties. The above content can be identified using a known analytical method such as ¹ H-NMR.

-Oxygen permeability-
The polyurethane resin contained in the resin layer preferably has an oxygen permeability of 100 mL / ( ^m2・ day ・ atm) or less at 23 ° C. and 50% RH when converted into a sheet having a thickness of 25 μm, preferably 50 mL. It is more preferably less than / (m ² · day · atm), more preferably 25 mL / (m ² · day · atm) or less, and more preferably 10 mL / (m ² · day · atm) or less. Even more preferable. In the present specification, the oxygen permeability is measured using an oxygen permeability measuring device (OX-TRAN2 / 22 manufactured by MOCON) under the conditions of 23 ° C. and 50% RH.

As the polyurethane resin, a synthetic product may be used, and examples thereof include the polyurethane resin described in International Publication No. 2015/016869. As the polyurethane resin, a commercially available product may be used. For example, "Takelac W-based (trade name)", "Takelac WPB-based (trade name)", and "Takelac WS-based (trade name)" manufactured by Mitsui Chemicals, Inc. may be used. ) ”, And specifically, Takelac WPB-341 is exemplified. Examples of other commercially available products include "HPU W-003" (hydroxyl value 235 mgKOH / g) manufactured by Dainichiseika Kogyo Co., Ltd.

(Silane coupling agent)
From the viewpoint of improving the bending resistance of the resin layer, the resin layer is preferably formed by blending a silane coupling agent in addition to the above-mentioned water-suspendable polymer.

The silane coupling agent is a compound having at least one alkoxysilyl group and at least one reactive functional group other than the alkoxysilyl group in the molecule. The alkoxysilyl group may be any of a monoalkoxysilyl group, a dialkoxysilyl group and a trialkoxysilyl group, but a trialkoxysilyl group is preferable from the viewpoint of reactivity.

Examples of the reactive functional group other than the alkoxysilyl group include a vinyl group, an epoxy group, a styryl group, a (meth) acryloyloxy group, an amino group, an isocyanato group, a ureido group and an acid anhydride group. Among these, an amino group, an epoxy group, and an acid anhydride group are preferable, and an amino group is more preferable.

Examples of the epoxy group-containing silane coupling agent include 3-glycidoxypropyltrimethoxysilane, 3-glycidoxypropyltriethoxysilane, 3-glycidoxypropylmethyldiethoxysilane, and 2- (3,4-epoxycyclohexyl). ) Ethyltrimethoxysilane and the like are exemplified.

Examples of the amino group-containing silane coupling agent include 3-aminopropyltrimethoxysilane, 3-aminopropyltriethoxysilane, N-2- (aminoethyl) -3-aminopropylmethyldimethoxysilane, and N-2- (aminoethyl). ) -3-Aminopropyltrimethoxysilane, 3-triethoxysilyl-N- (1,3-dimethylbutylidene) propylamine, N-phenyl-3-aminopropyltrimethoxysilane, etc. are exemplified, among these. 3-Aminopropyltriethoxysilane is preferred.

Examples of the acid anhydride group-containing silane coupling agent include 3-trimethoxysilylpropyl succinic acid anhydride and the like.

As the silane coupling agent, a commercially available product may be used, for example, KBM-303, KBM-402, KBM-403, KBE-402, KBE-403, KBM-602, KBM manufactured by Shin-Etsu Chemical Co., Ltd. -603, KBM-903, KBE-903, KBE-9103P, KBM-573, X-12-967C and the like are exemplified.

The blending amount of the silane coupling agent is preferably 0.03 part by mass or more, more preferably 0.1 part by mass or more, still more preferably 0.2 part by mass or more with respect to 100 parts by mass of the water-suspendable polymer. It is particularly preferably 0.3 parts by mass or more, and preferably 10 parts by mass or less, more preferably 8 parts by mass or less, still more preferably 6 parts by mass or less, and particularly preferably 5 parts by mass or less.

The coating amount of the resin layer is not particularly limited, but the solid content is more preferably 0.1 g / m ² or more, more preferably 1 g / m ² or more, and 10 g / m ² or less. It is preferably 5 g / m ² or less, and more preferably 5 g / m 2. The method for forming the resin layer is not particularly limited, but it is preferable to apply an aqueous solution of a water-suspending polymer or an aqueous medium such as an aqueous dispersion and dry to form the resin layer.

<Physical characteristics of base paper for thin-film deposition paper>
(Wet tension)
In the base paper for thin-film deposition paper of the present embodiment, the wetting tension of the resin layer surface measured in accordance with JIS K 6768: 1999 is 50 mN / m or more, preferably 55 mN / m or more. By setting the wetting tension on the surface of the resin layer within the above range, the polarity of the surface of the resin layer is increased, and the adhesion between the resin layer and the thin-film deposition layer formed on the layer is improved. As a result, it is considered that the obtained vapor-film-deposited paper can exhibit excellent barrier properties. The upper limit of the wetting tension on the surface of the resin layer is not particularly limited, but is 70 mN / m or less. For example, the wetting tension can be adjusted within the above range by adjusting the components used for the resin layer.

(Print / surf surface roughness)
The printed surf surface roughness of the surface of the resin layer measured in accordance with JIS P 8151: 2004 is 2.5 μm or less, preferably 1.5 μm or less in the base paper for thin-film deposition paper of the present embodiment. By setting the print surf surface roughness of the resin layer surface within the above range, a thin-film deposition layer with few defects can be formed on the resin layer. As a result, it is considered that the obtained vapor-film-deposited paper can exhibit excellent barrier properties. The lower limit of the print surf surface roughness of the resin layer surface is not particularly limited, but is 0.1 μm or more. For example, the print surf surface roughness can be adjusted within the above range by adjusting the coating amount of the resin layer or the like.

(thickness)
The thickness of the base paper for thin-film deposition paper of the present embodiment is preferably 10 μm or more, more preferably 30 μm or more, preferably 100 μm or less, and more preferably 80 μm or less.

The method for producing the base paper for vapor-deposited paper of the present embodiment is not limited, and for example, as a method for producing the base paper for vapor-deposited paper having a clay coat layer and a resin layer on at least one surface of a paper substrate in this order. It is preferably formed by applying and drying a coating liquid for a clay coat layer containing an inorganic pigment and a binder, and then applying and drying a coating liquid for a resin layer containing a water-suspendable polymer.

[Thin-film deposition paper]
The present invention also provides a thin-film deposition paper having a thin-film deposition layer on the resin layer of the base paper for thin-film deposition paper.

<Embedded layer>
The thin-film deposition layer is at least one of a layer made of metal and a layer made of ceramic. That is, the thin-film deposition layer may be any of a metal layer, a ceramic layer, and a laminate of a metal layer and a ceramic layer. When the vapor-deposited layer is a laminate of a metal layer and a ceramic layer, the metal layer may be on the resin layer side of the base paper for vapor-deposited paper, and the ceramic layer may be on the resin layer side of the base paper for vapor-deposited paper. It may be, and is not particularly limited.

The thin-film deposition layer may be a layer made of metal, a layer made of ceramic, or a laminate thereof, but a layer made of metal is preferable. When the vapor-filmed layer is a layer made of metal, specific examples of the metal include aluminum and titanium. These may be used alone or in combination of two or more. Among these, aluminum is preferable. When the vapor-filmed layer is a layer made of ceramic, specific examples of the ceramic include silicon oxide, titanium oxide, aluminum oxide and the like. These may be used alone or in combination of two or more. Among these, silicon oxide and aluminum oxide are preferable.

That is, the vapor-deposited layer is more preferably any of a layer made of aluminum, a layer made of silicon oxide, a layer made of titanium oxide, a layer made of aluminum oxide, and a laminate thereof, and the layer made of aluminum and oxidation. Any of a layer made of silicon, a layer made of aluminum oxide, and a laminate thereof is more preferable, and a layer made of aluminum is particularly preferable.

(thickness)
The thickness of the thin-film deposition layer is preferably 1 nm or more, more preferably 2 nm or more, further preferably 3 nm or more, preferably 1000 nm or less, and more preferably 500 nm or less. It is preferably 100 nm or less, and more preferably 100 nm or less. From the viewpoint of barrier properties, the thickness of the thin-film deposition layer is preferably 10 nm or more, more preferably 25 nm or more, and more preferably 80 nm or less, more preferably 70 nm. .. Further, the thickness of the thin-film deposition layer is preferably 4 nm or more, more preferably 5 nm or more, and more preferably 100 nm or less, preferably 70 nm, from the viewpoint of adhesion to other layers and cost. It is more preferably less than or equal to, and particularly preferably 60 nm or less.

<Overcoat layer>
The thin-film vapor deposition paper of the present embodiment preferably has an overcoat layer containing a polyurethane resin on the thin-film deposition layer. The thin-film vapor-deposited paper of the present embodiment has a certain barrier property by having a thin-film film layer, but by having an overcoat layer containing a polyurethane resin on the thin-film film layer, the oxygen barrier property can be further improved. Further, the vapor-filmed layer is not easily damaged by processing such as bending, and even if it is damaged, the oxygen barrier property can be ensured by the overcoat layer, and excellent oxygen barrier property can be maintained.

Examples of the polyurethane-based resin as the binder contained in the overcoat layer include those exemplified as the polyurethane-based resin of the resin layer, and for example, one or more selected from the group consisting of polyurethane-based resin dispersions and emulsions can be prepared. It is more preferable that it can be prepared into a polyurethane-based resin dispersion or an emulsion, and it is even more preferable that it can be prepared into a polyurethane-based resin dispersion.

The polyurethane resin contained in the overcoat layer preferably contains at least one selected from the group consisting of a structural unit derived from metaxylylene diisocyanate and a structural unit derived from hydrogenated metaxylylene diisocyanate. When the polyurethane resin contains at least one of the constituent units derived from metaxylylene diisocyanate and the constituent units derived from hydrogenated metaxylylene diisocyanate, the constituent units derived from metaxylylene diisocyanate and the constituent units derived from polyisocyanate with respect to the total amount of the constituent units derived from polyisocyanate. The total content of the constituent units derived from the hydrogenated metaxylylene diisocyanate is preferably 50 mol% or more. Such a polyurethane-based resin exhibits a high cohesive force due to hydrogen bonds and a stacking effect between xylylene groups, and thus has excellent gas barrier properties.

(Oxygen permeability)
The polyurethane resin contained in the overcoat layer preferably has an oxygen permeability of 100 mL / (m ² · day · atm) or less at 23 ° C. and 50% RH when converted into a 25 μm thick sheet, preferably 50 mL. It is more preferably less than / (m ² · day · atm), more preferably 25 mL / (m ² · day · atm) or less, and more preferably 10 mL / (m ² · day · atm) or less. Even more preferable.

The polyurethane-based resin as the binder contained in the overcoat layer may be the same type as the polyurethane-based resin contained in the resin layer of the base paper for vapor-film deposition paper described above, or may be of a different type, but is the same. It is preferable that the type is. Further, as the resin layer of the base paper for thin-film deposition paper, a synthetic product or a commercially available product listed as usable may be used.

The content of the polyurethane resin in the overcoat layer is preferably 80% by mass or more, more preferably 90% by mass or more, still more preferably 95% by mass or more, still more preferably 99% by mass or more. Is. The upper limit is not particularly limited, but is 100% by mass or less.

The overcoat layer may contain other resins and additives as long as the effects of the present invention are not impaired. Examples of the additive include surfactants, pigments, antioxidants, antistatic agents, dyes, plasticizers, lubricants, mold release agents and the like. When the polyurethane resin is used as an aqueous dispersion, it is preferable to use a dispersant in order to disperse the polyurethane resin in an aqueous medium and obtain a uniform overcoat layer film.

The coating amount of the overcoat layer is preferably 0.1 g / m ² or more, more preferably 0.2 g / m ² or more, and 0.3 g / m ² or more in terms of solid content. It is particularly preferable, and it is preferably 10 g / m ² or less, more preferably 7 g / m ² or less, and particularly preferably 4 g / m ² or less.

The thickness of the overcoat layer is preferably 0.1 μm or more, more preferably 0.2 μm or more, particularly preferably 0.3 μm or more, and preferably 10 μm or less. It is more preferably 7 μm or less, and particularly preferably 4 μm or less. When the thickness of the overcoat layer is 0.1 μm or more and 10 μm or less, the protection against the vapor-filmed layer is improved, the paper is excellent in dissociation during recycling, and the recyclability is also excellent.

The method for forming the overcoat layer is not particularly limited, but it is preferably formed by applying an aqueous medium such as an aqueous solution of a polyurethane resin or an aqueous dispersion and drying it.

In the vapor-filmed paper of the present embodiment, the overcoat layer may be the outermost layer. Even if the overcoat layer is the outermost layer, it does not impair the design of the vapor-filmed layer having a glossy feeling. When the vapor deposition layer is provided on both sides, an overcoat layer may be provided on one side or both sides thereof. Among these, it is preferable to have an overcoat layer on one side. Having an overcoat layer on one side is excellent in production efficiency.

[Manufacturing method of thin-film vapor deposition paper]
There is no limitation on the method for producing the thin-film vapor-deposited paper of the present embodiment, but the surface on which the clay coat layer and the resin layer of the base paper for thin-film deposition having the resin layer in this order are provided on at least one surface of the paper base material. , A step of depositing at least one of metal and ceramic to form a vapor deposition layer, and a step of applying a coating liquid for an overcoat layer on the vapor deposition layer and drying it to form an overcoat layer. It is preferable to include it.

As a method for depositing metal or ceramic, a method of vacuum-depositing metal or ceramic directly on the surface of the resin layer of the base paper for vapor deposition paper is preferable.

It is preferable to form the overcoat layer directly on the thin-film deposition layer from the viewpoint of efficiently protecting the vapor-film deposition layer and enhancing the barrier property. As a method for forming the overcoat layer, it is preferable to apply a liquid for the overcoat layer and dry the overcoat layer. By applying a coating liquid for an overcoat layer to form an overcoat layer, an overcoat layer having a relatively thin film of 10 μm or less can be formed. By forming such a relatively thin overcoat layer, excellent dissociation property can be imparted, and a thin-film film having excellent recyclability can be obtained.

Examples of the coating liquid for the overcoat layer used here include a solution using an organic solvent that dissolves the polyurethane resin, a dispersion liquid that uses an organic solvent that disperses the polyurethane resin, and a dispersion liquid that uses an aqueous medium. Therefore, a dispersion liquid using an aqueous medium is preferable from the viewpoint of coatability and environmental load.

Examples of the method for applying the coating liquid for the overcoat layer include a bar coat method, a blade coat method, a squeeze coat method, an air knife coat method, a roll coat method, a gravure coat method, a transfer coat method, and the like. Or a coating machine such as a slit die coater may be used.

The coated vapor-deposited paper coated with the coating liquid for the overcoat layer can be dried to remove the organic solvent or the aqueous medium, and a thin-film vapor-deposited paper having the overcoat layer on the vapor-deposited layer can be obtained.

Further, a heat seal layer containing a thermoplastic resin may be formed on the overcoat layer. Examples of the method for forming the heat seal layer include applying a thermoplastic resin solution or a thermoplastic resin dispersion liquid and drying the solution, extruding and laminating the layer. Among these, it is preferable to apply a thermoplastic resin solution or a thermoplastic resin dispersion and dry the obtained product.

The thermoplastic resin solution or thermoplastic resin dispersion used here is a solution using an organic solvent that dissolves the thermoplastic resin, a dispersion liquid that uses an organic solvent that disperses the thermoplastic resin, or a dispersion liquid that uses an aqueous medium. From the viewpoint of coatability and environmental load, a dispersion liquid using an aqueous medium is preferable.
The thermoplastic resin suitable for the dispersion liquid using an aqueous medium may be either a natural resin or a synthetic resin, and for example, a starch derivative, casein, shrak, polyvinyl alcohol and its derivatives, acrylic resin, ionomer resin, and malein. Examples thereof include acid-based resins, urethane-based resins, polyester-based resins, styrene-butadiene-based resins, vinyl chloride-based resins, and polyolefin-based resins.
More specifically, the acrylic resin includes an acrylic resin obtained by copolymerizing (meth) acrylic acid with its alkyl ester or styrene as a monomer component, a styrene-maleic acid resin, and a styrene-acrylic acid-maleic acid. Examples thereof include resins, water-soluble polyurethane resins, and water-soluble polyester resins.
As the ionomer-based resin, for example, ethylene-acrylic acid copolymer ionomer and ethylene-methacrylic acid ionomer are preferable. Here, the ionomer is a polymer neutralized with cations, and examples of the cations include ammonium ^ions (NH ₄₊ ) and organic ammonium ions in addition to metal ions. Examples of the metal ion include alkali metal ions such as lithium ion (Li ⁺ ), sodium ion (Na ⁺ ) and potassium ion (K ⁺ ), and alkaline earth metal such as magnesium ion (Mg ²⁺ ) and calcium ion (Ca ²⁺ ). Examples thereof include transition metal ions such as ions, zinc ions (Zn ²⁺ ), and copper ions (Cu ²⁺ ). Among these, sodium ion is preferable as the metal ion from the viewpoint of availability and the like.
Among these, select from starch derivatives, casein, shrak, polyvinyl alcohol and its derivatives, ionomer resins, acrylic resins, and maleic acids resins from the viewpoint of the stability of the coating liquid and the solvent resistance of the coating layer. At least one selected from a starch derivative, polyvinyl alcohol, polyvinyl alcohol derivative, ionomer resin, acrylic resin, and maleic acid resin is more preferable, and starch derivative, polyvinyl alcohol, polyvinyl alcohol derivative, and the like. At least one selected from the ionomer-based resin and the acrylic resin is further preferable, and at least one selected from the polyvinyl alcohol, the polyvinyl alcohol derivative, and the ionomer-based resin is even more preferable.

Examples of the method for applying the thermoplastic resin solution or the thermoplastic resin dispersion include a bar coating method, a blade coating method, a squeeze coating method, an air knife coating method, a roll coating method, a gravure coating method, and a transfer coating method. , A coating machine such as a fountain coater or a slit die coater may be used.

The coated vapor-deposited paper coated with the thermoplastic resin solution or the thermoplastic resin dispersion is dried to remove the organic solvent or the aqueous medium, and a coated vapor-deposited paper having a heat seal layer on the overcoat layer is obtained. Can be done.

The thickness of the heat seal layer is not particularly limited, but is preferably 1 μm or more and less than 15 μm. If it is 1 μm or more, sufficient heat sealability can be ensured. Further, if it is less than 15 μm, dissociability can be imparted, and a vapor-deposited paper having excellent recyclability can be obtained.

<Physical characteristics of thin-film vapor deposition paper>
(thickness)
The thickness of the vapor-filmed paper of the present embodiment is preferably 20 μm or more, more preferably 50 μm or more, preferably 200 μm or less, and more preferably 150 μm or less. The thickness of the thin-film vapor deposition paper is measured in accordance with JIS P 8118: 2014.

(Oxygen permeability)
The oxygen permeability of the vapor-deposited paper of the present embodiment at 23 ° C. and 50% RH is preferably 1.0 mL / (m ² · day · atm) or less, and 0.5 mL / (m ² · day · atm). The following is more preferable (lower limit: 0 mL / ( ^m2・ day ・ atm)). The oxygen permeability of the vapor-deposited paper is measured by the method described in Examples.

(Water vapor transmission rate)
The water vapor transmission rate of the vapor-filmed paper of the present embodiment at 40 ° C. and 90% RH is preferably 1.0 g / (m ² · day) or less, and is 0.7 g / (m ² · day) or less. Is more preferable (lower limit: 0 g / (m ² · day)). The water vapor transmission rate of the vapor-deposited paper is measured by the method described in the examples.

(Heat seal peeling strength)
In the vapor-deposited paper of the present embodiment, the heat-sealed layers are heat-sealed at 160 ° C., 0.2 MPa, and 1 second, and the maximum load when the test piece has a width of 15 mm and a T-shaped peeling at a tensile speed of 300 mm / min. The heat seal peeling strength is preferably 2N / 15 mm or more. If it is within the above range, it is excellent in suitability as a barrier package. The lower limit of the heat seal peeling strength is not particularly limited, but is, for example, 20 N / 15 mm or less.

The vaporized paper of the present embodiment can be suitably used as a packaging material for foods such as coffee, confectionery, milk, pharmaceuticals, medical products, electronic parts, etc. by taking advantage of the above-mentioned excellent barrier properties, and is highly recyclable. Is also excellent.

Hereinafter, the features of the present invention will be described in more detail with reference to Examples and Comparative Examples. The materials, amounts used, ratios, treatment contents, treatment procedures, etc. shown in the following examples can be appropriately changed as long as they do not deviate from the gist of the present invention. Therefore, the scope of the present invention should not be construed as limiting by the specific examples shown below. Unless otherwise specified, "%" and "parts" represent "% by mass" and "parts by mass", respectively. The operations of Examples and Comparative Examples were carried out under the conditions of room temperature (20 to 25 ° C.) and normal humidity (40 to 50% RH) unless otherwise specified.

<Example 1>
80 parts by mass of kaolin (Contour Xtreme manufactured by Imeris, aspect ratio 33, average particle diameter d50: 0.26 μm), 20 parts by mass (solid content) of a styrene-acrylic resin binder (JONCRYL HSL-9012 manufactured by BASF), and Was mixed to prepare a coating liquid for a clay coat layer. The above clay is applied to the glossy surface of single-gloss paper (broad-leaved wood ratio 100%, nice human size 9 seconds, basis weight 50 g / m ² , thickness 60 μm, density 0.83 g / cm ³ , Oken type smoothness 430 seconds). The coating liquid for the coat layer was coated with Mayer bar and dried at 120 ° C. for 1 minute to form a clay coat layer (12 g / m ² , thickness 4.6 μm). Next, on the clay coat layer, an aqueous dispersion of a polyurethane resin binder having a thickness of 25 μm and an oxygen permeability (23 ° C., 50% RH) of 2.0 mL / ( ^m2・ day ・ atm) (Mitsui Chemicals). Takelac WPB-341: Glass transition temperature 130 ° C., solid content concentration 30%) 0.15 parts by mass of 3-aminopropyltriethoxysilane (KBE-903, manufactured by Shinetsu Chemical Industry Co., Ltd.) is mixed with 100 parts by mass. The prepared coating liquid for the resin layer is coated with Mayer bar and dried at 120 ° C. for 1 minute to form a resin layer (2 g / m ² , thickness 2 μm), and a base paper for vapor deposition paper (thickness 67 μm) is formed. Obtained.

<Example 2>
A base paper for vapor-deposited paper was obtained in the same manner as in Example 1 except that the coating amount of the resin layer was 1 g / m ² (thickness 1 μm).

<Example 3>
3-Aminopropyltriethoxysilane (Shin-Etsu Chemical Co., Ltd.) in 100 parts by mass of an aqueous dispersion of a polyester resin binder (Elitel KT-8803 manufactured by Unitika Co., Ltd .: glass transition temperature 65 ° C., solid content concentration 30%, saturated copolymer polyester resin) Examples except that a resin layer (2 g / m ² , thickness 2 μm) was formed using a coating liquid for a resin layer prepared by mixing 0.15 parts by mass of KBE-903, manufactured by Kogyo Co., Ltd. In the same manner as in No. 1, a base paper for vapor deposition paper was obtained.

<Comparative Example 1>
Ethylene-acrylic acid copolymer (Zyxen AC manufactured by Sumitomo Seika Co., Ltd., glass transition temperature 80 ° C or less, solid content concentration 29% by mass) 3-aminopropyltriethoxysilane (manufactured by Shin-Etsu Chemical Industry Co., Ltd.) in 100 parts by mass KBE-903) The same as in Example 1 except that the resin layer (2 g / m ² , thickness 2 μm) was formed by using the coating liquid for the resin layer prepared by mixing 0.145 parts by mass. , A base paper for vapor deposition paper was obtained.

<Comparative Example 2>
3-Aminopropyltriethoxysilane (KBE-903, manufactured by Shin-Etsu Chemical Industry Co., Ltd.) in 100 parts by mass of styrene-acrylic resin (JONCRYL HSL-9012 manufactured by BASF, glass transition temperature 5 ° C. or lower, solid content concentration 40% by mass) ) The vapor-deposited paper in the same manner as in Example 1 except that the resin layer (2 g / m ² , thickness 2 μm) was formed by using the coating liquid for the resin layer prepared by mixing 0.20 parts by mass. I got a base paper.

<Comparative Example 3>
A base paper for vapor deposition was obtained in the same manner as in Example 1 except that the resin layer was not formed.

<Comparative Example 4>
A base paper for thin-film deposition paper was obtained in the same manner as in Example 3 except that the rough surface of the single-gloss paper was coated.

<Evaluation of base paper for thin-film deposition paper>
The following evaluations were made on the base paper for thin-film deposition paper obtained in Examples and Comparative Examples.

[Wet tension]
Wetting tension on the surface of the resin layer was measured using a wetting reagent (mixed solution for wetting tension test manufactured by Kanto Chemical Co., Inc.) in accordance with JIS K 6768: 1999.

[Print / Surf Surface Roughness]
The print surf surface roughness of the resin layer surface was measured according to JIS P 8151: 2004 using a print surf surface roughness tester manufactured by Lorentzen & Wettre.

[Glass-transition temperature]
A part of the resin layer of the base paper for vapor deposition was carved out, and the glass transition temperature was measured according to JIS K 7121: 1987. The glass transition temperature is shown in Table 1 as the glass transition temperature of the resin contained in the resin layer.

<Preparation of thin-film deposition paper>
An aluminum thin-film vapor deposition layer (thickness 50 nm) was formed on the resin layer of the base paper for thin-film deposition paper obtained in Examples and Comparative Examples. An aqueous dispersion of a polyurethane resin binder having an oxygen permeability (23 ° C., 50% RH) of 2.0 mL / ( ^m2・ day ・ atm) on the aluminum vapor deposition layer of a 25 μm thick sheet (Mitsui Chemicals, Inc.) Takelac WPB-341) was coated with Mayer bar and dried at 120 ° C. for 1 minute to form an overcoat layer (0.5 g / m ² , thickness: 0.5 μm). Further, on the overcoat layer, an aqueous dispersion of an ethylene / acrylic acid copolymer ammonium salt (effective content 29.2% by mass, Zyxen AC, acrylic acid copolymerization ratio 20 mol%, melting point: 95 ° C., Sumitomo Seika (Manufactured by Co., Ltd.) was diluted with water so that the effective content was 20% by mass, coated with Mayer bar, and then dried at 120 ° C. for 1 minute to form a heat seal layer (5 μm) to obtain a vapor-deposited paper. .. When ¹ H-NMR measurement was performed on the polyurethane resin used for the resin layer and the overcoat layer, the content of the constituent units derived from mexylylene diisocyanate was 50 mol% with respect to the total amount of the constituent units derived from polyisocyanate. That was all.

<Evaluation of thin-film deposition paper>
[Oxygen permeability]
Using an oxygen permeability measuring device (OX-TRAN2 / 22 manufactured by MOCON), the oxygen permeability of the paper laminate was measured under the conditions of a temperature of 23 ° C. and a relative humidity of 50%. The lower the oxygen permeability value, the better the oxygen barrier property.

[Water vapor transmission rate]
In accordance with JIS Z 0208: 1976 (cup method) B method (temperature 40 ° C ± 0.5 ° C, relative humidity 90% ± 2%), the overcoat layer of the paper laminate or the vapor deposition layer of the vapor-deposited paper is inside ( It was placed so as to come to the low humidity side), and the water vapor permeability was measured. The lower the value of water vapor transmission rate, the better the water vapor barrier property.

[Heat seal peeling strength]
A set of thin-film vaporized papers were stacked so that the heat-sealing layers faced each other, and heat-sealed using a heat-sealing tester (TP-701-B manufactured by Tester Sangyo) at 160 ° C., 0.2 MPa, and 1 second. Subsequently, the heat-sealed test piece was cut into a width of 15 mm, T-shaped peeled at a tensile speed of 300 mm / min using a tensile tester, and the maximum recorded load was taken as the heat-sealed peeling strength.

The vapor-deposited paper produced by using the base paper for thin-film vapor deposition of Examples 1 to 3 has lower oxygen permeability and water vapor permeability than the vapor-deposited paper produced by using the base paper for thin-film deposition paper of Comparative Examples 1 to 4. , Had excellent barrier properties.

Claims (15)

A base paper for thin-film deposition paper having a clay coat layer and a resin layer on at least one surface of a paper substrate in this order.
The surface of the resin layer has a wetting tension of 50 mN / m or more measured according to JIS K 6768: 1999, and a print surf surface roughness measured according to JIS P 8151: 2004 of 2. Base paper for vapor deposition paper with a thickness of .5 μm or less. The base paper for vapor-deposited paper according to claim 1, wherein the resin layer contains a resin having a glass transition temperature of 50 ° C. or higher. The base paper for vapor-deposited paper according to claim 1 or 2, wherein the resin layer contains a water-suspendable polymer. The base paper for vapor-deposited paper according to any one of claims 1 to 3, wherein the water-suspendable polymer contained in the resin layer is at least one selected from the group consisting of polyester-based resin and polyurethane-based resin. The vapor-filmed paper according to claim 4, wherein the polyurethane-based resin has an oxygen permeability of 100 mL / (m ² , day, atm) or less at 23 ° C. and 50% RH when converted into a sheet having a thickness of 25 μm. Base paper. The vapor-deposited paper according to claim 4 or 5, wherein the polyurethane-based resin contains at least one selected from the group consisting of a structural unit derived from metaxylylene diisocyanate and a structural unit derived from hydrogenated metaxylylene diisocyanate. Base paper. 4. The polyurethane resin has a total content of 50 mol% or more of the constituent units derived from metaxylylene diisocyanate and the constituent units derived from hydrogenated metaxylylene diisocyanate with respect to the total amount of the constituent units derived from polyisocyanate. The base paper for vaporized paper according to any one of 6 to 6. The base paper for vapor-deposited paper according to any one of claims 1 to 7, wherein the clay coat layer contains an inorganic pigment and a binder, and the inorganic pigment has an aspect ratio of 50 or less and an average particle size of 5 μm or less. .. The base paper for vapor-deposited paper according to claim 8, wherein the inorganic pigment is kaolin. Claimed that the binder contained in the clay coat layer is one or more selected from the group consisting of styrene-butadiene resin, styrene- (meth) acrylic resin, olefin-unsaturated carboxylic acid copolymer, and polylactic acid. Item 8. The base paper for vaporized paper according to Item 8 or 9. The base paper for vapor-deposited paper according to any one of claims 1 to 10, wherein the clay coat layer and the resin layer are formed by using an aqueous medium. A vapor-deposited paper having a vapor-deposited layer on the resin layer of the base paper for vapor-deposited paper according to any one of claims 1 to 11. The vapor-filmed layer has an overcoat layer containing a polyurethane resin, and the polyurethane resin contained in the overcoat layer is composed of a structural unit derived from metaxylylene diisocyanate and a structural unit derived from hydrogenated metaxylylene diisocyanate. The vapor-deposited paper according to claim 12, which contains at least one selected from the group. A heat-sealing layer containing a thermoplastic resin is provided on the overcoat layer, and the heat-sealing layers are heat-sealed under the conditions of 160 ° C., 0.2 MPa, and 1 second. The vapor-deposited paper according to claim 13, wherein the maximum load heat seal peeling strength at the time of T-shaped peeling at / min is 2N / 15 mm or more. Oxygen permeability at 23 ° C. and 50% RH is 1.0 mL / (m ² · day · atm) or less, and water vapor permeability at 40 ° C. and 90% RH is 1.0 g / (m ² · day). The vapor-deposited paper according to any one of claims 12 to 14, which is as follows.