Patent Application
20220177726
The present invention is one that provides a composition having gas barrier properties. A coating agent containing this gas barrier composition and a laminate obtained by applying this coating agent are also provided.
Packaging materials for the packaging of foods, pharmaceutical products, or similar articles are expected to prevent the spoiling of the contents, oxidization caused by oxygen in particular. To cope with this demand, the industry has used a barrier film made of resin, which is acknowledged to have relatively high oxygen barrier properties, or a laminate made using such a barrier film as a film substrate (multilayer film).
The oxygen barrier resin has been one that contains a hydrogen-bonding group, which is highly hydrophilic, in its molecule, typified by polyacrylic acid or polyvinyl alcohol. Packaging materials made of such resins deliver excellent oxygen barrier properties under dry conditions. In conditions of high humidity, however, they have the disadvantage that the hydrophilicity of the resins causes a great decrease in their oxygen barrier properties.
To overcome such disadvantages, a known method for preparing a gas barrier packaging material includes stacking a layer of a polycarboxylic acid-based polymer and a layer containing a polyvalent metal compound on top of each other on a substrate and allowing the two layers to react to form a polyvalent metal salt of polycarboxylic acid. The production of such a gas barrier packaging material, however, is cumbersome; it requires multiple coating solutions and multiple rounds of coating.
PTL 1: Japanese Unexamined Patent Application Publication No. 2007-112114
The present invention addresses the problem of providing a composition that delivers high barrier properties in fewer coating steps.
After extensive research, the inventors found that a particular composition for gas barrier purposes that contains a carboxyl-containing resin, a divalent metal compound, and an alcohol can solve this problem.
That is, the present invention is one that provides a composition for gas barrier purposes containing at least one carboxyl-containing resin (A), at least one divalent metal compound (B), and at least one alcohol (C), wherein alcohol (C) content of the composition is between 85 and 98 wt %, and water content of the composition is 1% or less.
The present invention, furthermore, is one that provides a gas barrier coating agent containing this composition for gas barrier purposes and a laminate having a substrate and a coat layer obtained by applying this coating agent.
In addition, the present invention is one that provides a packaging material having this laminate.
The composition according to the present invention is superior in storage stability because divalent metal compound(s) is kept stable therein. The composition, furthermore, is suitable for use as a coating agent for gas barrier purposes. The applied coating film exhibits high barrier properties in a one-component system, which means the composition delivers high barrier properties in fewer coating steps.
The laminate obtained by applying this composition to a substrate is suitable for use as a packaging material by virtue of its superior gas barrier properties. In particular, the laminate is suitable for use as a packaging material for which barrier properties are essential, such as one for foods, daily necessities, or electronic materials or for medical purposes.
The laminate, furthermore, is highly resistant to heat and wet heat, making it also suitable for use as a packaging material in heat sterilization, such as boiling or retorting.
The present invention provides a composition for gas barrier purposes containing at least one carboxyl-containing resin (A), at least one divalent metal compound (B), and at least one alcohol (C). The alcohol (C) content of the composition is between 85 and 98 wt %, and the water content of the composition is 1% or less
A resin (A) according to the present invention is characterized in that it contains at least one carboxyl group. The carboxyl group contained may be carboxylic anhydride(s).
Preferably, the carboxyl-containing resin (A) is one whose acid value is between 50 to 800 mg KOH/g because this leads to improved barrier performance. It is particularly preferred that the acid value be between 80 and 800 mg KOH/g. When the acid value of the resin (A) is 80 mg KOH/g or more, ionic bonding will proceed to a sufficient extent that the composition will achieve high barrier performance.
Acid value is the amount of potassium hydroxide in mg required to neutralize acid present in 1 g of the sample. Specifically, the acid value can be measured by the method of dissolving a weighed sample in any solvent in which the sample dissolves, e.g., the solvent of toluene/methanol=70/30 by volume, adding some drops of a 1% alcoholic solution of phenolphthalein, and then adding a 0.1 mol/L alcoholic solution of potassium hydroxide dropwise and observing the point where the color changes. The acid value can be determined by the following equation for calculation.
Acid value (mg KOH/g)=(V×F×5.61)/S
V: Consumption of the 0.1 mol/L alcoholic solution of potassium hydroxide (mL)
F: The factor of the 0.1 mol/L alcoholic solution of potassium hydroxide
S: Amount of sample collected (g)
5.61: Equivalent of potassium hydroxide in 1 mL of the 0.1 mol/L alcoholic solution of potassium hydroxide (mg)
If the sample is a solution of the resin, the acid value of the resin (mg KOH/g) can be determined by the following equation for calculation.
Acid value of the resin (mg KOH/g)=Acid value of the solution of the resin (mg KOH/g)/NV (%)×100
NV: Nonvolatile content (%)
If the sample does not dissolve well in an organic solvent but separates to make the measurement difficult, the acid value can be measured by the following method instead.
Acid value (mg KOH/g-resin) is a value calculated by the following equation using an FT-IR (JASCO, FT-IR 4200) and a factor (f) obtained from a calibration curve constructed with a solution of maleic anhydride in chloroform and the absorbance (I) of the peak for the expansion of the anhydrous ring of maleic anhydride (1780 cm-1) and that (II) of the peak for the expansion of the carbonyl groups of maleic acid (1720 cm-1) in a solution of a maleic anhydride-modified polyolefin.
Acid value (mg KOH/g-regin)=[(Absorbance (I)×(f)×2×Molecular weight of potassium hydroxide×1000 (mg)+Absorbance (II)×(f)×Molecular weight of potassium hydroxide×1000 (mg))/Molecular weight of maleic anhydride]
Molecular weight of maleic anhydride, 98.06; molecular weight of potassium hydroxide, 56.11
The molecular weight of a carboxyl-containing resin (A) according to the present invention is not critical. Preferably, the number-average molecular weight is between 300 and 1,200,000; this ensures the composition will form a coating well. It is particularly preferred that the number-average molecular weight be between 500 and 1,000,000.
The weight-average molecular weight of a carboxyl-containing resin (A) according to the present invention can be calculated by measuring it by the method of gel permeation chromatograph (GPC).
The resin structure of the carboxyl-containing resin (A) is not critical. Preferably, it is preferred that the resin (A) be a carboxyl-containing vinyl resin.
Examples of carboxyl-containing vinyl resins include polymers of polymerizable unsaturated monomers having carboxyl group(s). Examples of polymerizable unsaturated monomers having carboxyl group(s) include unsaturated carboxylic acids, such as (meth)acrylic acid, 2-carboxyethyl (meth)acrylate, crotonic acid, itaconic acid, maleic acid, and fumaric acid;
monoesters (half-esters) of unsaturated dicarboxylic acids and saturated monohydric alcohols, such as monomethyl itaconate, mono-n-butyl itaconate, monomethyl maleate, mono-n-butyl maleate, monomethyl fumarate, and mono-n-butyl fumarate;
monovinyl esters of saturated dicarboxylic acids, such as monovinyl adipate and monovinyl succinate;
adducts of saturated polycarboxylic anhydrides, such as succinic anhydride, glutaric anhydride, and phthalic anhydride, and hydroxy-containing vinyl monomers; and monomers such as those obtained through addition reaction between lactones and carboxyl-containing monomers like the listed ones.
A carboxyl-containing resin (A) according to the present invention may be a homopolymer of a polymerizable unsaturated monomer having carboxyl group(s) as described above or may be a copolymer made with multiple polymerizable unsaturated monomers having carboxyl group(s). A copolymer of a polymerizable unsaturated monomer having carboxyl group(s) and another monomer that can be copolymerized with it may also be used.
Examples of monomers that can be copolymerized with a polymerizable unsaturated monomer having carboxyl group(s) include those such as the following:
(1) (meth)acrylates having a C1 to C22 alkyl group, such as methyl (meth)acrylate, ethyl (meth)acrylate, propyl (meth)acrylate, n-butyl (meth)acrylate, t-butyl (meth)acrylate, hexyl (meth)acrylate, heptyl (meth)acrylate, octyl (meth)acrylate, nonyl (meth)acrylate, decyl (meth)acrylate, dodecyl (meth)acrylate, tetradecyl (meth)acrylate, hexadecyl (meth)acrylate, stearyl (meth)acrylate, octadecyl (meth)acrylate, and docosyl (meth)acrylate;
(2) (meth)acrylates having an ali-alkyl group, such as cyclohexyl (meth)acrylate, isobornyl (meth)acrylate, dicyclopentanyl (meth)acrylate, and dicyclopentenyloxyethyl (meth)acrylate;
(3) (meth)acrylates having an aromatic ring, such as benzoyloxyethyl (meth)acrylate, benzyl (meth)acrylate, phenylethyl (meth)acrylate, phenoxydiethylene glycol (meth)acrylate, and 2-hydroxy-3-phenoxypropyl (meth)acrylate;
(4) acrylates having a hydroxyalkyl group, such as hydroxyethyl (meth)acrylate; hydroxypropyl (meth)acrylate, hydroxybutyl (meth)acrylate, glycerol (meth)acrylate; lactone-modified hydroxyethyl (meth)acrylate, and (meth)acrylates having a polyalkylene glycol group, such as polyethylene glycol (meth)acrylate and polypropylene glycol (meth)acrylate;
(5) esters of unsaturated dicarboxylic acids, such as dimethyl fumarate, diethyl fumarate, dibutyl fumarate, dimethyl itaconate, dibutyl itaconate, methyl ethyl fumarate, methyl butyl fumarate, and methyl ethyl itaconate;
(6) styrene derivatives, such as styrene, α-methylstyrene, and chlorostyrene;
(7) diene compounds, such as butadiene, isoprene, piperylene, and dimethylbutadiene;
(8) vinyl halides and vinylidene halides, such as vinyl chloride and vinyl bromide;
(9) unsaturated ketones, such as methyl vinyl ketone and butyl vinyl ketone;
(10) vinyl esters, such as vinyl acetate and vinyl butyrate;
(11) vinyl ethers, such as methyl vinyl ether and butyl vinyl ether;
(12) vinyl cyanides, such as acrylonitrile, methacrylonitrile, and vinylidene cyanide;
(13) acrylamide and amides derived by its alkyd substitution;
(14) N-substituted maleimides, such as N-phenylmaleimide and N-cyclohexylmaleimide
(15) fluorine-containing ethylenic unsaturated monomers, such as fluorine-containing α-olefins, like vinyl fluoride, vinylidene fluoride, trifluoroethylene, chlorotrifluoroethylene, bromotrifluoroethylene, pentafluoropropylene, and hexafluoropropylene; (per) fluoroalkyl-perfluorovinyl ethers in which the number of carbon atoms in the (per)fluoroalkyl group is from 1 to 18, like trifluoromethyl trifluorovinyl ether, pentafluoroethyl trifluorovinyl ether, and heptafluoropropyl trifluorovinyl ether; (per)fluoroalkyl (meth)acrylates in which the number of carbon atoms in the (per)fluoroalkyl group is from 1 to 18, like 2,2,2-trifluoroethyl (meth)acrylate, 2,2,3,3-tetrafluoropropyl (meth)acrylate, 1H,1H,5H-octafluoropentyl (meth)acrylate, 1H,1H,2H,2H-heptadecafluorodecyl (meth)acrylate, and perfluoroethyloxyethyl (meth)acrylate;
(16) silyl-containing (meth)acrylates, such as γ-methacryloxypropyltrimethoxysilane; and
(17) N,N-dialkylaminoalkyl (meth)acrylates, such as N,N-dimethylaminoethyl (meth)acrylate, N,N-diethylaminoethyl (meth)acrylate, and N,N-diethylaminopropyl (meth)acrylate.
One of these polymerizable unsaturated monomers may be used alone, or two or more may be used in combination.
The carboxyl-containing resin (A) can be obtained by just polymerizing (copolymerizing) the monomer(s) using a process that is known and commonly used; the form of copolymerization is not critical. The resin (A) can be produced by addition polymerization in the presence of a catalyst (polymerization initiator) and can be any of a random copolymer, block copolymer, graft copolymer, etc. As for the copolymerization technique, too, known polymerization techniques can be used, such as bulk polymerization, solution polymerization, suspension polymerization, and emulsion polymerization.
A metal compound (B) according to the present invention is characterized in that it is a divalent metal compound.
A divalent metal compound (B) is a compound of a divalent metal. Examples of divalent metal compounds (B) include zinc compounds, magnesium compounds, calcium compounds, manganese compounds, iron compounds, cobalt compounds, nickel compounds, and copper compounds. Zinc compounds, magnesium compounds, and calcium compounds are particularly preferred. One of these metal compounds may be used alone, or two or more may be used in combination.
Preferably, the divalent metal compound (B) is an oxide, hydroxide, or carbonate of a divalent metal. A mixture of such compounds may also be used.
Specific examples of preferred divalent metal compounds (B) are zinc oxide, magnesium oxide, and calcium oxide. Zinc oxide and magnesium oxide are particularly preferred.
Preferably, the divalent metal compound (B) is in particulate form. More preferably, the divalent metal compound (B) is fine particles having an average diameter of 500 nm or less and 10 nm or more. It is particularly preferred that the divalent metal compound (B) be fine particles having an average diameter between 20 nm and 300 nm.
The average diameter of particles in this context can be measured using a dynamic-light-scattering particle size distribution analyzer, such as LB-500 (HORIBA).
An alcohol (C) according to the present invention can be an alcohol that is known and commonly used. Specific examples include methanol, ethanol, propanol, butanol, hexanol, and pentanol. Methanol, ethanol, propanol, butanol are preferred, and propanol is particularly preferred.
A composition according to the present invention for gas barrier purposes is characterized in that it contains at least one carboxyl-containing resin (A), at least one divalent metal compound (B), and at least one alcohol (C), all as described above. Of these, the percentage of the alcohol (C) is between 85 and 98 wt %, and the water content of the composition is 1% or less. When the alcohol (C) and water are in these ranges, the divalent metal compound (B) is stable in the composition. The divalent metal compound (B), therefore, forms ionic bonds with the carboxyl-containing resin (A) and produces gas barrier properties only after the composition is applied and dried. Stable when stored in its normal state, the composition is eminently suitable for use as a coating agent for gas barrier purposes. The coating agent forms a gas barrier coat layer in a one-component system.
For the gas barrier composition according to the present invention, the nonvolatile content is between 1 wt % and 15 wt % of the composition. Preferably, the percentage of the carboxyl-containing resin (A) and divalent metal compound (B) combined to the total nonvolatile content is between 90 and 100 wt %. When this percentage is in this range, the composition produces sufficient gas barrier properties. It is particularly preferred that this percentage be between 95 and 100 wt %.
As for the proportion of the carboxyl-containing resin (A) to the divalent metal compound (B), it is preferred that the divalent metal compound (B) constitute 15 to 60 wt % of the carboxyl-containing resin (A) and divalent metal compound (B) combined. When this percentage is in this range, the composition combines good gas barrier properties with spreadability. It is particularly preferred that this percentage be between 20 and 50 wt %.
The gas barrier composition according to the present invention may contain materials other than the carboxyl-containing resin (A), divalent metal compound (B), and alcohol (C).
The gas barrier composition according to the present invention may contain a solvent other than the alcohol (C). Solvents compatible with the alcohol (C) are preferred. Examples include ethylene glycol, propylene glycol, and glycerol.
The composition according to the present invention may contain additives unless they will ruin the advantages of the present invention. Examples of additives include coupling agents, silane compounds, phosphoric acid compounds, organic fillers, inorganic fillers, stabilizers (antioxidant, heat stabilizer, ultraviolet absorber, etc.), plasticizers, antistatic agents, lubricants, anti-blocking agents, coloring agents, nucleators, oxygen scavengers (compounds capable of trapping oxygen), and tackifiers. One of these additives alone or a combination of two or more is used.
Examples of coupling agents include known and commonly used ones. Examples include silane coupling agents, titanium coupling agents, zirconium coupling agents, and aluminum coupling agents.
For silane coupling agents, known and commonly used ones can be used. Examples include epoxy-containing silane coupling agents, such as 3-glycidoxypropyltrimethoxysilane, 3-glycidoxypropyltriethoxysilane, 3-glycidoxypropylmethyldiethoxysilane, and 2-(3,4 epoxycyclohexyl)ethyltrimethoxysilane; amino-containing silane coupling agents, such as 3-aminopropyltrimethoxysilane, N-2-(aminoethyl)-3-aminopropylmethyldimethoxysilane, 3-triethoxysilyl-N-(1,3-dimethylbutylidene)propylamine, and N-phenyl-γ-aminopropyltrimethoxysilane; (meth)acryloyl-containing silane coupling agents, such as 3-acryloxypropyltrimethoxysilane and 3-methacryloxypropyltriethoxysilane; and isocyanate-containing silane coupling agents, such as 3-isocyanatopropyltriethoxysilane.
Examples of titanium coupling agents include isopropyl triisostearoyl titanate, isopropyl trioctanoyl titanate, isopropyl dimethacrylisostearoyl titanate, isopropyl isostearoyl diacryl titanate, isopropyl tris(dioctyl pyrophosphate) titanate, tetraoctyl bis(ditridecyl phosphite) titanate, tetra(2,2-diallyloxymethyl-1-butyl) bis(ditridecyl) phosphite titanate, bis(dioctyl pyrophosphate) oxyacetate titanate, and bis(dioctyl pyrophosphate) ethylene titanate.
Examples of zirconium coupling agents include zirconium acetate, ammonium zirconium carbonate, and zirconium fluoride.
Examples of aluminum coupling agents include acetalkoxyaluminum diisopropylates, aluminum diisopropoxymonoethylacetoacetate, aluminum tris ethylacetoacetate, and aluminum tris acetylacetonate.
Examples of silane compounds include alkoxysilanes, silazanes, and siloxanes. Examples of alkoxysilanes include methyltrimethoxysilane, dimethyldimethoxysilane, phenyltrimethoxysilane, methyltriethoxysilane, dimethyldiethoxysilane, phenyltriethoxysilane, n-propyltrimethoxysilane, n-propyltriethoxysilane, hexyltrimethoxysilane, hexyltriethoxysilane, octyltriethoxysilane, decyltrimethoxysilane, and 1,6-bis(trimethoxysilyl)hexane, and trifluoropropyltrimethoxysilane. Examples of silazanes include hexamethyldisilazane. Examples of siloxanes include those containing a hydrolyzable group.
As a type of additive, examples of inorganic fillers include inorganic substances, such as metals, metal oxides, resins, and minerals, and composites thereof. Specific examples of inorganic fillers include silica, alumina, titanium, zirconia, copper, iron, silver, mica, talc, aluminum flakes, glass flakes, and clay minerals.
Examples of compounds capable of trapping oxygen include low-molecular-weight organic compounds that react with oxygen, such as hindered phenolic compounds, vitamin C, vitamin E, organic phosphorus compounds, gallic acid, and pyrogallol, and transition metal compounds, for example of cobalt, manganese, nickel, iron, or copper.
Examples of tackifiers include xylene resins, terpene resins, phenolic resins, and rosin resins. Adding a tackifier helps improve the adhesion of the composition in its freshly applied state to substrates. Preferably, the amount of tackifier added is between 0.01 and 5 parts by mass per 100 parts by mass of the resin composition as a whole.
Applying a coating agent that contains a composition according to the present invention for gas barrier purposes to a substrate gives a laminate having gas barrier properties. Once the coating agent is applied to a substrate, its volatile components are eliminated, causing the carboxyl-containing resin (A) and the divalent metal compound (B) to form ionic bonds. The resulting crosslinked structure gives the coating barrier properties.
A coating agent according to the present invention is stable when stored, free of changes such as gelation. By virtue of the presence of alcohol(s) (C), ionic bonding between carboxyl-containing resin(s) (A) and divalent metal compound(s) (B) is blocked until the agent is applied.
In a two-layer gas barrier laminate like those that have existed, furthermore, the ionic bonding between acid groups and metal compound(s) is limited to the interface. Crosslinks, therefore, extend only in two dimensions, and the inventors presume this causes the coating to have only low gas barrier properties as a result. The coating agent according to the present invention, the inventors presume, delivers high barrier properties because it is of one-component type and, therefore, forms a coat layer inside which crosslinks extend three-dimensionally.
The material for the substrate is not critical; the manufacturer can choose a suitable material according to the purpose of use. Examples include wood, metal, metal oxides, plastic, paper, silicone, and modified silicone, and a substrate obtained by joining different materials together may also be used. The shape of the substrate is not critical; the substrate can be in any shape selected according to the purpose, such as flat-plate, sheet-shaped, or a three-dimensional shape having curvature throughout or in part of it. The hardness, thickness, etc., of the substrate are not critical either.
If the laminate is used as a packaging material, the substrate is, for example, a piece of paper, plastic, metal, or metal oxide.
It is not critical how to apply the coating agent; known and commonly used coating techniques can be used. Examples include spraying, spin coating, dipping, roll coating, blade coating, doctor roll coating, doctor blading, curtain coating, slit coating, screen printing, inkjet coating, and dispensing.
The coat layer obtained by applying the coating agent will have denser ionic bonds therein when the applied coating agent is dried. It is therefore preferred that the application be followed by a drying step. The drying step may be drying at room temperature or may be forced drying, such as heating, vacuum drying, or blow drying.
The laminate may be a multilayer one having a top layer on its substrate and coat layer. The top layer may be placed before the coating agent is dried or may be placed after the coating agent is dried. The top layer can be of any kind and can be, for example, a layer of wood, metal, metal oxide, plastic, paper, silicone, or modified silicone. Alternatively, an uncured resin solution may be applied over the coat layer and cured or dried into a top layer.
(Gaseous Substances that can be Prevented from Penetrating)
Examples of gases a resin composition according to the present invention or a laminate including this resin composition can intercept include inert gases, such as carbon dioxide, nitrogen, and argon, alcoholic substances, such as methanol, ethanol, and propanol, and phenols, such as phenol and cresol, as well as oxygen. Fragrance substances that are low-molecular-weight compounds, such as soy sauce, Worcestershire sauce, miso, limonene, menthol, methyl salicylate, coffee, cocoa shampoo, and conditioner.
<Packaging Material and that for Use in Heat Sterilization>
Superior in gas barrier properties, the laminate according to the present invention is suitable for use as a packaging material for which gas barrier properties are a demand. In particular, foods, daily necessities, electronic materials, contents for medical purposes, etc., are suitable applications of the packaging material according to the present invention because in such applications have high barrier properties are required.
The laminate, furthermore, is highly resistant to heat and wet heat, making it also suitable for use as a packaging material in heat sterilization, such as boiling or retorting.
The following describes the present invention by examples. The present invention, however, is not limited to these examples. The units are by weight unless stated otherwise.
Definition: The molecular weight of the repeating unit of polyacrylic acid (hereinafter: sometimes abbreviated to PAA) is 72. Usually, one molecule of zinc oxide (molecular weight, 81.4) (hereinafter: sometimes abbreviated to ZnO) contributes to reaction with two molecules of the repeating unit of PAA (molecular weight, 72×2) to form a salt. The formula in which PAA and ZnO are mixed in the proportions of PAA weight:ZnO weight=144/82.4=100/57 is referred to as adding one equivalent of ZnO.
A PAA solution with a solids concentration: 2% was obtained by dissolving, in a flask, a PAA powder having a number-average molecular weight of 250,000 (AC-10LHPK, Toagosei): 20 g by stirring it in boiling isopropyl alcohol (hereinafter sometimes abbreviated to IPA), Kanto Chemical: 980 g.
A PAA solution with a solids concentration: 20% was obtained by dissolving, in a flask, a PAA powder having a number-average molecular weight of 9000 (AC-10P, Toagosei): 200 g by stirring it in boiling IPA: 800 g. This solution was diluted with IPA to give 9000-Da PAA solutions with solids concentrations of 2%, 5%, 10%, and 15%.
For a liquid dispersion of ZnO, a ZnO solution with a solids concentration: 20% was obtained by mixing ZnO having a diameter of primary particles of 20 nm (Sakai Chemical Industry Co., Ltd., FINEX-50): 200 g and IPA: 800 g together, dispersing the mixture in a bead mill (Kotobuki Co., Ltd.: Ultra Aspec Mill UAM-015) using 0.3-mm zirconia beads for 1 hour, and then isolating the beads by sieving. This solution was diluted with IPA to give liquid dispersions of ZnO in IPA with solids concentrations of 2%, 5%, 10%, and 15%. The diameter of particles of ZnO in these liquid dispersions was 88 nm.
Coating agent 1 was obtained by mixing 100 g of the 2% PAA solution obtained in Preparation Example 1 and 57.0 g of the 2% ZnO solution obtained in Preparation Example 8 together. Coating agent 1 was subjected to an appearance test of the coating agent.
In addition to this, laminate 1 was prepared by applying the coating agent to a substrate. The resulting laminate was subjected to an appearance test of the coat layer and a gas barrier test of the laminate.
The results are presented in Table 3.
The appearance test of the coating agent was performed visually. The grades were as follows.
4: No fine particles separate out
3: A small quantity of fine particles separate out
2: A medium quantity of fine particles separate out
1: The separation of fine particles is significant
The appearance test of the coat layer was performed visually. The substrate was a piece of polyethylene terephthalate film (TOYOBO ESTER Film's E5100; thickness, 12 μm), and laminate 1 was prepared by applying coating agent 1 thereto by the application method described below. For the resulting coat layer, its appearance test was conducted visually. The grades were as follows.
4: Pale white, and no fine particles separate out
3: Pale white, and a small quantity of fine particles separate out
2: Pale white, and a medium quantity of fine particles separate out
1: Pale white, and the separation of fine particles is significant
A barrier coat film was obtained by preparing Matsuo Sangyo Co., Ltd.: K303 bar No. 1, yellow/6 μm, K303 bar No. 2, red/12 μm, K303 bar No. 3, green/24 μm, and K303 bar No. 4, black/40 μm, applying the mixed solution to a piece of PET film (TOYOBO ESTER Film's: E5100: thickness: 12 μm), and drying the coating at 120° C.: 1 minute. The bar was selected so that the weight of the barrier coat material on the dried sample would be about 1.0 g/m2. The weight of applied coating was calculated by making ten coating samples under each set of conditions, weighing a 10 cm×10 cm cutout of each sample and averaging the measured weights, and subtracting the average weight of ten substrate sheets of the same area from the determined average. Based on the results, the right coating bar was chosen.
The grades were:
4, Pale white, and no fine particles separate out;
3, Pale white, and a small quantity of fine particles separate out;
2, Pale white, and a medium quantity of fine particles separate out; and
1, Pale white, and the separation of fine particles is significant.
Oxygen permeability was tested using the barrier coat film on PET (thickness: 12 μm) obtained in the previous section, including the substrate. The measurement of oxygen permeability was carried out in accordance with JIS-K7126 (equal-pressure method) using MOCON's OX-IRAN 1/50 oxygen transmission rate analyzer in 23° C. temperature and 0% RH humidity and 23° C. temperature and 90% RH humidity atmospheres. RH stands for relative humidity. The unit of oxygen permeability is cc/day·atm·m2.
For Examples 2 to 11 and Comparative Examples 1 to 3, a coating agent and a laminate were tested as in Example 1 except that the formula was changed to that in Table 3. The results are presented in Tables 3 to 5.
In Examples 1 to 5, the 25-kDa PAA and ZnO solutions were mixed to make the ZnO equivalence factor vary from 0.6 to 1.4. The mixed solution and the coating were in good appearance, and the oxygen permeability was also good. In Examples 6 and 7, water was added to a percentage of 0.5% or 1.0% of the mixed solution as a whole. The appearance of the mixed solution and the coating, although somewhat worse, was practically acceptable, and the oxygen permeability was also good. In Examples 8 to 11, solids content levels of 2% to 15% were studied using 9000-Da PAA and a constant ZnO equivalence factor of 1. The mixed solution and the coating were in good appearance, and the oxygen permeability was also good.
In Comparative Examples 1 and 2, water was added to a percentage of 1.5% of the entire system with each of the 25-kDa and 9000-Da PAA solutions and the ZnO solution. The appearance of the mixed solution and the coating and the oxygen permeability were degraded significantly. In Comparative Example 3, the 9000-Da PAA and ZnO solutions were studied at a solids concentration of 20%. The appearance of the mixed solution of the coating and the oxygen permeability were poor.
Overall, the results indicated that in the context of a composition for gas barrier purposes containing a carboxyl-containing resin, a divalent metal compound, and an alcohol, good appearance of the mixed solution and the coating is combined with good oxygen permeability when the alcohol content of the composition is between 85 and 98 wt % and when the water content of the composition is 1% or less.
The composition according to the present invention is superior in storage stability because divalent metal compound(s) is kept stable therein. The composition, furthermore, is suitable for use as a coating agent for gas barrier purposes. The applied coating film exhibits high barrier properties in a one-component system, which means the composition delivers high barrier properties in fewer coating steps.
The laminate obtained by applying this composition to a substrate is suitable for use as a packaging material by virtue of its superior gas barrier properties. In particular, the laminate is suitable for use as a packaging material for which barrier properties are essential, such as one for foods, daily necessities, or electronic materials or for medical purposes.
The laminate, furthermore, is highly resistant to heat and wet heat, making it also suitable for use as a packaging material in heat sterilization, such as boiling or retorting.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2019-069852 | Apr 2019 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2020/014010 | 3/27/2020 | WO | 00 |
