Classifications

• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D129/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal, or ketal radical; Coating compositions based on hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Coating compositions based on derivatives of such polymers
  • C09D129/02—Homopolymers or copolymers of unsaturated alcohols
  • C09D129/06—Copolymers of allyl alcohol
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D129/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal, or ketal radical; Coating compositions based on hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Coating compositions based on derivatives of such polymers
  • C09D129/02—Homopolymers or copolymers of unsaturated alcohols
  • C09D129/04—Polyvinyl alcohol; Partially hydrolysed homopolymers or copolymers of esters of unsaturated alcohols with saturated carboxylic acids
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F216/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical
  • C08F216/02—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical by an alcohol radical
  • C08F216/04—Acyclic compounds
  • C08F216/06—Polyvinyl alcohol ; Vinyl alcohol
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
  • C08J7/04—Coating
  • C08J7/048—Forming gas barrier coatings
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
  • C09D7/40—Additives
  • C09D7/60—Additives non-macromolecular
  • C09D7/63—Additives non-macromolecular organic
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J2329/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal, or ketal radical; Hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Derivatives of such polymer
  • C08J2329/02—Homopolymers or copolymers of unsaturated alcohols
  • C08J2329/04—Polyvinyl alcohol; Partially hydrolysed homopolymers or copolymers of esters of unsaturated alcohols with saturated carboxylic acids
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/04—Oxygen-containing compounds
  • C08K5/13—Phenols; Phenolates

Definitions

• the present invention relates to a coating used as a coating agent, a gas barrier layer, etc., and a laminate packaging material comprising the coating.
• Amine-modified polyvinyl alcohols such as vinyl alcohol-vinylamine copolymers have, for example, high oxygen barrier properties as disclosed in Patent Document 1, and have excellent adhesiveness among polyvinyl alcohol-based resins, and can be used as anchor agents. It is known that a film can be formed by coating on a plastic film without using it. Therefore, it is increasingly being used as a gas barrier layer in food packaging applications. Conventionally, as disclosed in, for example, Patent Documents 2 and 3, an inorganic layered compound is added to a gas barrier layer containing a vinyl alcohol-vinylamine copolymer for the purpose of enhancing oxygen barrier properties under high humidity conditions. known to be mixed.
• amine-modified polyvinyl alcohol has low water resistance because its basic skeleton is polyvinyl alcohol. Therefore, the coating film formed by amine-modified polyvinyl alcohol easily peels off and swells when moisture adheres or when packaging an article containing a large amount of moisture, and loses its function as a packaging material. Therefore, in the food field, applications are limited to fields that do not contain much moisture, such as dried foods and unbaked sweets, and that do not require boiling sterilization or retort sterilization.
• cross-linking agents such as titanium chelate, boric acid, epichlorohydrin, and aldehydes
• the coating agents tend to gel, and it is difficult to impart sufficient water resistance.
• Patent Documents 2 and 3 when an inorganic stratiform compound is contained in a coating agent, the oxygen barrier property under high humidity is enhanced, but water resistance cannot be sufficiently imparted. Transparency is also reduced.
• the present invention improves the water resistance of a coating film formed from a coating agent containing amine-modified polyvinyl alcohol, and can maintain good gas barrier properties without peeling of the coating film even when used for various purposes.
• the object is to provide a coating agent.
• the present inventors found that the above problems can be solved by blending a compound (A) having a specific structure with a coating agent containing amine-modified polyvinyl alcohol, and completed the present invention below. let me That is, the present invention provides the following [1] to [22].
• [1] At least one compound selected from the group consisting of an amine-modified polyvinyl alcohol, a compound (A1) represented by the following formula (1), and a compound (A2) represented by the following formula (2) ( A) and a coating agent.
• R 1 to R 6 each independently represent a carboxyl group, a sulfo group, a hydroxyl group, a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, an aryl group having 6 to 12 carbon atoms, and a halogen atom. and one of R 1 to R 6 is either a carboxyl group or a sulfo group, and two or three of R 1 to R 6 are hydroxyl groups.
• R 11 to R 18 are each independently a carboxyl group, a sulfo group, a hydroxyl group, a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, an aryl group having 6 to 12 carbon atoms, or a halogen atom. , one of R 11 to R 18 is either a carboxyl group or a sulfo group, and two or three of R 11 to R 18 are hydroxyl groups.
• the benzoic acids are 2,4-dihydroxybenzoic acid, 3,4-dihydroxybenzoic acid, 3,5-dihydroxybenzoic acid, 3,4,5-trihydroxybenzoic acid, and 2,4,6-
• [6] The coating agent according to any one of [1] to [5] above, wherein the amount of compound (A) is 30 parts by mass or less per 100 parts by mass of amine-modified polyvinyl alcohol.
• the amine-modified polyvinyl alcohol is a vinyl alcohol-vinylamine copolymer containing a vinylamine residue and a vinyl alcohol residue.
• the polyvinyl alcohol-based resin contained in the coating agent consists of the amine-modified polyvinyl alcohol, or consists of a polyvinyl alcohol-based resin other than the amine-modified polyvinyl alcohol and the amine-modified polyvinyl alcohol, above [1] to [ 7].
• the amine-modified amount of the polyvinyl alcohol resin contained in the coating agent is 1 part by mass or more and 40 parts by mass or less with respect to 100 parts by mass of the polyvinyl alcohol resin, above [1] to [10] Coating agent according to any one of the.
• the present invention it is possible to improve the water resistance of a coating film formed from a coating agent containing an amine-modified polyvinyl alcohol, and maintain good gas barrier properties without peeling of the coating film even when used for various purposes. .
• the coating agent of the present invention contains amine-modified polyvinyl alcohol and compound (A).
• Amine-modified polyvinyl alcohol is modified polyvinyl alcohol having an amino group. By containing amine-modified polyvinyl alcohol in the coating agent, the gas barrier properties of the coating film formed from the coating agent can be improved, and the adhesion to plastic films and the like can also be improved.
• Amine-modified polyvinyl alcohol is typically a vinyl alcohol-vinylamine copolymer containing a vinylamine residue and a vinyl alcohol residue, and may be a block copolymer thereof or a random copolymer. There may be one or a combination thereof.
• the method for producing the vinyl alcohol-vinylamine copolymer is not particularly limited. It can be obtained by hydrolyzing the copolymer.
• N-vinylamide units and vinyl ester units are preferably hydrolyzed at a ratio of, for example, 70% or more, preferably 90% or more, and more preferably 95% or more.
• Specific examples of N-vinylamide include N-vinylformamide and N-vinylacetamide, and among them N-vinylformamide is preferred.
• Specific examples of vinyl esters include vinyl acetate, vinyl formate, vinyl propionate, vinyl butyrate, vinyl isotrate, vinyl pivalate, vinyl caproate, vinyl caprylate, and vinyl neodecanoate. Vinyl acetate is preferred.
• the molar ratio of the vinylamine residue and the vinyl alcohol residue is not particularly limited, but is, for example, 1/99 or more and 50/50 or less, preferably 3 /97 or more and 40/60 or less, more preferably 5/95 or more and 25/75 or less.
• a vinyl alcohol-vinylamine copolymer typically has the following structure.
• m is 0 mol% or more and 15 mol% or less
• n is 50 mol% or more and 99 mol% or less
• x is 0 mol% or more and 30 mol% or less
• y is It is 1 mol % or more and 50 mol % or less.
• the amine-modified polyvinyl alcohol preferably has a viscosity of 4% by mass aqueous solution at 23°C of 100 mPa ⁇ s or less, more preferably 50 mPa ⁇ s or less, and even more preferably 20 mPa ⁇ s or less. Moreover, it is preferably 2 mPa ⁇ s or more, preferably 3 mPa ⁇ s or more, and more preferably 4 mPa ⁇ s or more.
• the viscosity of an aqueous solution with a concentration of 4% by mass is measured with a Brookfield viscometer in accordance with JIS-Z-8803:2011.
• the amine-modified polyvinyl alcohol may be the main component in the coating agent.
• the content of the amine-modified polyvinyl alcohol in the coating agent is, for example, 50% by mass or more, preferably 60% by mass or more, more preferably 70% by mass or more, and still more preferably 75% by mass or more, based on the total solid content. is.
• the content of the amine-modified polyvinyl alcohol is preferably 94% by mass or less, more preferably 92% by mass or less, and even more preferably 90% by mass or less, based on the total solid content.
• amine-modified polyvinyl alcohol alone may be used as the polyvinyl alcohol-based resin, or polyvinyl alcohol-based resin other than amine-modified polyvinyl alcohol may be added in addition to amine-modified polyvinyl alcohol.
• Polyvinyl alcohol-based resins other than amine-modified polyvinyl alcohol are preferably mixed with amine-modified polyvinyl alcohol so as to have the amine-modified amount described later. Therefore, the coating agent according to another preferred embodiment preferably contains a polyvinyl alcohol-based resin as a main component.
• the content of the polyvinyl alcohol-based resin (that is, the total content of the amine-modified polyvinyl alcohol and other polyvinyl alcohol-based resins) is based on the total solid content, for example 50% by mass or more, preferably It is 60% by mass or more, more preferably 70% by mass or more, and still more preferably 75% by mass or more.
• the content of the polyvinyl alcohol-based resin is preferably 94% by mass or less, more preferably 92% by mass or less, and even more preferably 90% by mass or less, based on the total solid content.
• the amount of amine modification of the polyvinyl alcohol resin contained in the coating agent is, for example, 1 part by mass or more and 40 parts by mass or less, preferably 2 parts by mass or more and 30 parts by mass or less, more preferably, with respect to 100 parts by mass of the polyvinyl alcohol resin. is 3 parts by mass or more and 20 parts by mass or less, more preferably 6 parts by mass or more and 18 parts by mass or less.
• the amount of amine modification means the content of structural units having an amine group (typically, vinylamine residues) with respect to 100 parts by mass of the polyvinyl alcohol-based resin.
• Compound (A) is at least one compound selected from the group consisting of compound (A1) represented by formula (1) below and compound (A2) represented by formula (2) below.
• R 1 to R 6 are each independently a carboxyl group, a sulfo group (—SO 3 H), a hydroxyl group, a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, or an aryl group having 6 to 12 carbon atoms. or a substituent such as a halogen atom, one of R 1 to R 6 is a carboxyl group or a sulfo group, and two or three of R 1 to R 6 are hydroxyl groups.
• R 11 to R 18 are each independently a substituent such as a carboxyl group, a sulfo group, a hydroxyl group, a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, an aryl group having 6 to 12 carbon atoms, or a halogen atom. and one of R 11 to R 18 is a carboxyl group or a sulfo group, and two or three of R 11 to R 18 are hydroxyl groups.
• the compound (A) has a structure in which a plurality of hydroxyl groups and one carboxyl group or sulfo group are bonded to the aromatic ring, thereby appropriately cross-linking the amine-modified polyvinyl alcohol. Therefore, a cross-linked structure can be introduced into the coating film formed from the coating agent, and the water resistance can be improved. can be maintained.
• a general cross-linking agent with a high cross-linking effect generates a ketone group, etc., and yellowing and browning may occur, but the compound (A) tends to suppress yellowing and browning during cross-linking. Therefore, it becomes easy to improve the appearance of the coating film formed from the coating agent.
• the compound (A) is highly safe and can be used as a food additive depending on its structure, and can be suitably used for food applications.
• a coating agent containing amine-modified polyvinyl alcohol and compound (A) is relatively resistant to gelation and is easy to handle.
• the alkyl groups for R 1 to R 6 and R 11 to R 18 are preferably alkyl groups having 1 to 4 carbon atoms, more preferably alkyl groups having 1 or 2 carbon atoms.
• the alkyl group may be linear, but may have a branched structure or a cyclic structure. Specific examples of alkyl groups include methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, isobutyl group, sec-butyl group, tert-butyl group, n-pentyl group, n-hexyl group and cyclohexyl group. etc.
• the aryl group for R 1 to R 6 and R 11 to R 18 is preferably an aryl group having 6 to 9 carbon atoms.
• the aryl group may be a phenyl group, a naphthyl group, or an alkyl-substituted aryl group such as a tolyl group, a xylyl group, an ethylphenyl group, and a methylnaphthyl group.
• Halogen atoms for R 1 to R 6 and R 11 to R 18 include fluorine, chlorine, bromine and iodine atoms.
• one of R 1 to R 6 is a carboxyl group or a sulfo group, two or three of R 1 to R 6 are hydroxyl groups, and all of the rest are hydrogen atoms.
• Preferred specific examples of compound (A1) include dihydroxybenzenesulfonic acid, trihydroxybenzenesulfonic acid, dihydroxybenzoic acid, and trihydroxybenzoic acid.
• one of R 1 to R 6 is more preferably a carboxyl group, so dihydroxybenzoic acid and trihydroxybenzoic acid are more preferred.
• one of R 11 to R 18 is a carboxyl group or a sulfo group, two or three of R 11 to R 18 are hydroxyl groups, and all of the remaining are hydrogen atoms. and more preferably two of R 11 to R 18 are hydroxyl groups. Also, one of R 11 to R 18 is more preferably a carboxyl group.
• Examples of the compound (A2) represented by formula (2) include dihydroxynaphthalenesulfonic acid and dihydroxynaphthoic acid, with dihydroxynaphthoic acid being preferred.
• Specific examples of compound (A2) include 1,4-dihydroxy-2-naphthoic acid, 3,5-dihydroxy-2-naphthoic acid and 3,7-dihydroxynaphthoic acid.
• dihydroxynaphthoic acid is preferably a compound in which two hydroxy groups and one carboxylic acid are present in the same ring. - naphthoic acid.
• Compound (A) is preferably compound (A1) represented by formula (1), more preferably at least one benzoic acid selected from the group consisting of dihydroxybenzoic acid and trihydroxybenzoic acid. preferable.
• dihydroxybenzoic acid and trihydroxybenzoic acid it becomes easier to improve the water resistance of the film formed from the coating agent.
• these benzoic acids are highly safe and can be suitably used for food applications. Furthermore, yellowing or browning of the coating film and gelling of the coating agent tend to occur with difficulty.
• Dihydroxybenzoic acid and trihydroxybenzoic acid vary in performance such as water resistance depending on the positions of hydroxyl groups and carboxyl groups.
• Preferred specific examples of compound (A) from the viewpoint of water resistance include 2,3-dihydroxybenzoic acid, 2,4-dihydroxybenzoic acid, 2,5-dihydroxybenzoic acid, 2,6-dihydroxybenzoic acid, 3,4-dihydroxybenzoic acid, 3,5-dihydroxybenzoic acid, 2,4,6-trihydroxybenzoic acid, and 3,4,5-trihydroxybenzoic acid.
• 2,4-dihydroxybenzoic acid, 3,4-dihydroxybenzoic acid, 3,5-dihydroxybenzoic acid, 3,4,5-trihydroxybenzoic acid, and 2,4,6-trihydroxybenzoic acid from the viewpoint of improving water resistance while suppressing yellowing and browning, 2,4-dihydroxybenzoic acid, 3,4-dihydroxybenzoic acid, 3,5-dihydroxybenzoic acid, 2,4,6 -trihydroxybenzoic acid is more preferred, especially 3,4-dihydroxybenzoic acid, 3,5-dihydroxybenzoic acid and 2,4,6-trihydroxybenzoic acid.
• Dihydroxybenzoic acid is preferable from the viewpoint of further suppressing yellowing and browning.
• a compound (A) may be used individually by 1 type, and may use 2 types together.
• the compounding amount of compound (A) in the coating agent according to one embodiment is preferably 30 parts by mass or less with respect to 100 parts by mass of amine-modified polyvinyl alcohol.
• the compounding amount of the compound (A) is more preferably 28 parts by mass or less, still more preferably 25 parts by mass or less, and even more preferably 20 parts by mass or less with respect to 100 parts by mass of the amine-modified polyvinyl alcohol. .
• the compounding amount of the compound (A) is preferably 6 parts by mass or more with respect to 100 parts by mass of the amine-modified polyvinyl alcohol. By making it 6 mass parts or more, it becomes easy to make water resistance favorable.
• the compounding amount of the compound (A) is more preferably 8 parts by mass or more, still more preferably 10 parts by mass or more with respect to 100 parts by mass of the amine-modified polyvinyl alcohol.
• the coating agent contains polyvinyl alcohol-based resins other than amine-modified polyvinyl alcohol in addition to amine-modified polyvinyl alcohol as polyvinyl alcohol-based resins. Therefore, in the coating agent according to another preferred embodiment, the compounding amount of compound (A) is such that gelation, yellowing, and browning do not occur with respect to 100 parts by mass of the polyvinyl alcohol-based resin contained in the coating agent. From the viewpoint of improving water resistance while making it difficult to use, the amount is preferably 30 parts by mass or less, more preferably 28 parts by mass or less, still more preferably 25 parts by mass or less, and even more preferably 20 parts by mass or less.
• the amount of the compound (A) is preferably 6 parts by mass or more, more preferably 8 parts by mass or more, and still more preferably 100 parts by mass of the polyvinyl alcohol resin, from the viewpoint of easily improving the water resistance. It is 10 parts by mass or more.
• the coating agent of the present invention may contain additives other than the compound (A), and may contain, for example, an inorganic stratiform compound.
• the inorganic layered compound is an inorganic compound in which very thin unit crystal layers are superimposed to form one layered particle.
• Representative examples of inorganic layered compounds include hydrous silicates such as phyllosilicate minerals.
• Antigorite clay minerals such as chrysotile, smectite clay minerals such as montmorillonite, beidellite, nontronite, saponite, hectorite, sauconite, stevensite, vermiculite clay minerals such as vermiculite, muscovite, phlogopite, margarite, Examples include mica such as tetrasilic mica and teniolite, mica group clay minerals, and the like. These inorganic layered compounds are used singly or in combination of two or more. Among these inorganic layered compounds, smectite group clay minerals such as montmorillonite and mica group clay minerals such as water-swellable mica are preferred.
• the content of the inorganic stratiform compound in the coating agent is, for example, 5% by mass or more and 35% by mass or less, preferably 8% by mass or more and 30% by mass or less, based on the total solid content.
• the coating agent may contain additives other than the inorganic layered compound as additives other than the compound (A) as long as the effects of the present invention are not impaired.
• additives include, for example, antioxidants, weathering agents, heat stabilizers, lubricants, crystal nucleating agents, ultraviolet absorbers, plasticizers, antistatic agents, coloring agents, fillers other than inorganic layered compounds, antifoaming agents, Additives such as an agent, a silane coupling agent, and a surfactant can be used.
• the resin component constituting the coating agent may be amine-modified polyvinyl alcohol alone, but may contain resin components other than amine-modified polyvinyl alcohol as long as the effects of the present invention are not impaired.
• a hydroxyl group-containing resin other than modified polyvinyl alcohol may also be included.
• Specific examples include polyvinyl alcohol-based resins other than amine-modified polyvinyl alcohol.
• Polyvinyl alcohol-based resins other than amine-modified polyvinyl alcohol are not particularly limited, but unmodified polyvinyl alcohol can be mentioned.
• Unmodified polyvinyl alcohol is obtained by saponifying polyvinyl ester, and preferably consists of a vinyl alcohol residue, or a vinyl alcohol residue and a vinyl ester residue.
• the coating agent of the present invention contains a liquid medium such as water or an organic solvent, and is preferably diluted with the liquid medium.
• a liquid medium such as water or an organic solvent
• Each component constituting the coating agent described above is preferably dissolved or dispersed in a liquid medium.
• Organic solvents used for liquid media include, for example, monohydric alcohols, glycols, dimethylformamide, dimethylsulfoxide, and acetone. Examples of monohydric alcohols include methanol, ethanol, propanol, isopropanol, and butanol. Ethanol and isopropanol are preferred organic solvents.
• the coating agent is preferably a water-based coating agent using water as the liquid medium.
• water When water is used as the liquid medium, amine-modified polyvinyl alcohol and the like are easily dissolved in the liquid medium, and it is highly safe and can be suitably used for food applications.
• water-based coating agents water may be used alone as the liquid medium. They may be used together to form a mixed medium.
• the organic solvent used in combination is not particularly limited, monohydric alcohols are preferred, and ethanol is more preferred.
• the mass ratio of water and organic solvent (water/organic solvent) in the mixed medium is not particularly limited, but is, for example, 30/70 or more and 95/5 or less, preferably 50/50 or more and 90/10 or less.
• the solid content concentration in the coating agent is, for example, 0.5% by mass or more and 20% by mass or less, preferably 1% by mass or more and 12% by mass or less, from the viewpoint of film-forming properties, handling properties, solubility of each component, and the like. , more preferably 2% by mass or more and 8% by mass or less.
• the coating agent of the present invention can be produced by a general method for producing a coating agent. can be produced by mixing
• the coating film of the present invention is formed from the coating agent described above.
• the coating film of the present invention can be formed, for example, by applying a coating agent to a substrate and drying it as necessary.
• the amine-modified polyvinyl alcohol contained in the coating agent is preferably crosslinked by reacting with the compound (A).
• the compound (A) and amine-modified polyvinyl alcohol may already react in the coating agent before application to the substrate, or may react after application.
• the coating film of the present invention has a low oxygen permeability and can be suitably used as a gas barrier layer.
• a method for applying the coating agent to the substrate is not particularly limited, and a known method can be used.
• coating methods include gravure, roll coating, doctor knife, die coating, bar coating, dipping, spray coating, curtain coating, spin coating, flexo coating, screen coating, and brushing. and the like using a coating method.
• the surface of the base material to which the coating agent is applied is subjected to surface treatment such as corona treatment, ozone treatment, electron beam treatment, and application of an anchor coating agent in order to increase the adhesion between the base material and the coating film. may be
• drying the applied coating agent there is no particular limitation for drying the applied coating agent, and known means can be used. Drying should be carried out so that the liquid medium contained in the coating agent is volatilized. Drying includes, for example, drying by heating, drying by non-heating means such as reduced pressure, and drying by a combination thereof.
• the drying temperature by heating is, for example, 30 to 150° C., preferably 40 to 100° C.
• the drying time is, for example, 1 second to 24 hours, more preferably 10 seconds to 60 minutes.
• the coating amount of the coating film formed from the coating agent is, for example, 0.5 to 5.0 g/m 3 , preferably 1.0 to 2.0 g/m 3 as the total solid content after drying. When the coating amount is within the above range, the gas barrier properties and the like can be improved without increasing the thickness of the coating film more than necessary.
• the substrate is not particularly limited, it is preferably a resin film.
• the resin used for the resin film include polyethylene-based resins such as low-density polyethylene (LDPE), high-density polyethylene (HDPE), and linear low-density polyethylene (LLDPE), homopolypropylene, and random polypropylene.
• LDPE low-density polyethylene
• HDPE high-density polyethylene
• LLDPE linear low-density polyethylene
• homopolypropylene homopolypropylene
• random polypropylene random polypropylene.
• polypropylene resins such as ethylene-propylene copolymers, ethylene-butene copolymers, ethylene-hexene copolymers, ethylene-octene copolymers, poly-4-methylpentene-1, cyclic olefin resins, ethylene-acetic acid Vinyl copolymers, ethylene-methyl (meth)acrylate copolymers, ethylene-(meth)acrylic acid copolymers, olefinic resins such as ionomer resins, polyethylene terephthalate (PET), polybutylene terephthalate, polyethylene naphthalate, etc.
• PET polyethylene terephthalate
• PET polybutylene terephthalate
• polyethylene naphthalate etc.
• ester resins polyamide 6, polyamide 66, metaxylenediamine-adipic acid condensation polymer, amide resins such as polymethylmethacrylimide, acrylic resins, styrene resins, polyacrylonitrile resins, cellulose resins such as cellophane, poly Examples include vinyl chloride resin, polyvinylidene chloride resin, polyvinylidene fluoride resin, polycarbonate resin, and the like.
• the above resin may be used singly, or two or more resins may be mixed and used.
• the resin film may be a multilayer film, for example, a multilayer film in which each layer is formed of a different kind of resin.
• the resin film may be a non-stretched film or a stretched film.
• Preferred specific examples of the stretched film include stretched propylene-based resin films (OPP films), stretched PET films, stretched amide-based resin films, and the like.
• the resin film among the above, an olefin resin film, an ester resin film, and an amide resin film are preferable.
• the thickness of the substrate is not particularly limited, but is, for example, 1-500 ⁇ m, preferably 5-200 ⁇ m.
• the base material may be used as a heat-seal layer that adheres to other members by thermal fusion by appropriately selecting the type of thermoplastic resin used as the thermoplastic resin layer.
• the resin constituting the substrate is preferably an olefin resin.
• the present invention also provides a laminate having a substrate and the coating film formed on at least one surface of the substrate.
• the coating film is formed from the coating agent as described above.
• the coating film may be laminated on the surface of the substrate via another layer such as an anchor coat layer or a printed layer, or may be formed directly on the surface of the substrate.
• the coating film may be provided only on one side of the base material, or may be provided on both sides of the base material.
• a resin film or a printed layer may be further laminated on the laminate.
• a laminate having such a substrate and a coating film can be used as a gas barrier film because the coating film has excellent gas barrier properties.
• the laminate preferably has a heat seal layer as a separate layer from the base material described above.
• the heat seal layer is a layer that can be adhered to another layer by thermal fusion, and is preferably a thermoplastic resin layer.
• a thermoplastic resin used for the heat seal layer an olefin resin is preferable.
• the olefin-based resin those listed as resins usable for the substrate can be used, but polyethylene-based resins such as LDPE and LLDPE are more preferable.
• the thickness of the heat seal layer, which is a separate layer from the substrate is not particularly limited, but is, for example, 10 to 500 ⁇ m, preferably 20 to 200 ⁇ m. By setting the thickness of the heat-sealing layer within the above range, the heat-sealing layer can be imparted with appropriate heat-sealing properties without increasing the thickness of the laminate more than necessary.
• the heat seal layer may be provided on the side opposite to the surface of the base material on which the coating film is formed, but is preferably provided on the side of the surface of the base material on which the coating film is formed. That is, the laminate preferably has a layer structure in which a base material, a coating film, and a heat seal layer are provided in this order. By having such a layer structure, the laminate can be adhered to another film or the like by heating through the heat seal layer while protecting the coating film from both sides by the base material and the heat seal layer. Become.
• An adhesive layer may be provided between the heat-sealing layer and the coating film, and the heat-sealing layer is preferably adhered to the coated surface of the substrate via the adhesive layer.
• the adhesive layer may be formed from a known adhesive such as a dry lamination adhesive.
• the heat seal layer may be subjected to surface treatment such as corona treatment, ozone treatment, electron beam treatment, or application of an anchor coating agent on the side to be bonded to the substrate.
• the above-described laminate preferably has an oxygen permeability of 15 cc/m 2 ⁇ day ⁇ MPa or less, more preferably 12 cc/m 2 ⁇ day ⁇ MPa or less. , 10 cc/m 2 ⁇ day ⁇ MPa or less.
• the oxygen permeability is a value measured under an atmosphere of 23° C. and 0% RH according to JIS-K-7126-2 (isobaric method).
• Laminate strength is also increased.
• the laminate strength in such a case is preferably 2 N/15 mm or more, more preferably 4 N/15 mm or more.
• the higher the laminate strength, the better, and the upper limit is not particularly limited, but is, for example, 30 N/15 mm or less.
• the lamination strength is the peel strength when the base material with the coating film formed thereon is peeled off from the heat seal layer provided on the coating film. The measurement of the peel strength is preferably carried out under the conditions described in Examples.
• the laminate packaging material is a packaging material provided with the coating film described above.
• the laminate packaging material is preferably composed of a laminate having a coating film and a substrate as described in detail above.
• the laminate packaging material is preferably a packaging material that is used by being laminated on a member such as a film, and from such a viewpoint, the laminate packaging material preferably has a heat seal layer. Therefore, the laminate packaging material is preferably a laminate comprising a substrate, a coating film, and a heat seal layer. Moreover, you may have a printing layer on a coating film.
• Laminated packaging materials can be used for packaging various articles, but are preferably used for food applications.
• the laminated packaging material (laminate) of the present invention has a low oxygen permeability and good gas barrier properties, so that when used for food applications, the freshness of the packaged food can be maintained well for a long period of time. can.
• the coating film has good water resistance as described above, the laminated packaging material is suitably used for applications where moisture easily adheres, applications for boiling sterilization, and packaging of foods containing a large amount of moisture. be able to.
• the laminate packaging material is not particularly limited, it may be used in the form of a bag or pouch, for example.
• the laminated packaging material may be used by preparing two sheets, folding one sheet, overlapping the heat-sealing layers, and heat-sealing the heat-sealing layers. They may be heat-sealed together and used.
• the laminate packaging material is preferably made into a pouch or a bag by heat-sealing the heat-seal layers to each other and heat-sealing the heat-seal layers to another member.
• a vinyl alcohol-vinylamine copolymer manufactured by Sekisui Specialty Chemicals Co., Ltd., trade name "Ultiloc (registered trademark) 5003", amine modified amount 12 parts by mass
• A Add 25 parts by mass of 2,3-dihydroxybenzoic acid (first grade reagent) and dilute with a mixed solvent of water and ethanol (
• a biaxially oriented polyamide film (“Harden N1102” manufactured by Toyobo Co., Ltd.) was corona-treated on one side by using a wire bar set so that the coating amount of the obtained coating agent in a solution state was set to about 20 g/m 2 . was applied to the corona-treated surface of No. so that the coating amount after drying was 1.0 g/m 2 and dried in an oven at 80° C. for 2 minutes to form a coating film. After that, a dry laminate adhesive (product name: manufactured by Mitsui Chemicals, Inc., main agent: Takelac A-616, curing agent: Takenate A65) was applied to the coating film forming surface of the substrate.
• a dry laminate adhesive product name: manufactured by Mitsui Chemicals, Inc., main agent: Takelac A-616, curing agent: Takenate A65
• a base material with an adhesive applied to the coating film forming surface is pasted to the corona-treated surface of an LLDPE film (thickness: 70 ⁇ m, Toyobo Co., Ltd. “Rix L4102”) corona-treated on one side via an adhesive. to obtain a laminate packaging material.
• the obtained laminate packaging material was cured by being left in an environment of 40° C. for 72 hours. After that, the laminated film thus produced was cut into a certain size, the heat-sealable LLDPE surfaces were overlapped, one side was used as an opening, and the remaining three sides were heat-sealed to prepare a test pouch.
• Examples 2 to 12, 16, Comparative Examples 1 to 3 It was carried out in the same manner as in Example 1 except that the type of compound (A) and the amount added were changed as shown in Tables 1-4. As the compound (A) in each example and comparative example, a first-class reagent was used.
• Example 13 to 15, 17 As a polyvinyl alcohol resin, a vinyl alcohol-vinylamine copolymer (“Ultiloc (registered trademark) 5003”) was used in place of the vinyl alcohol-vinylamine copolymer alone so that the amount of amine modification described in Tables 3 and 4 was achieved. In addition, a mixture of polyvinyl alcohol resin (manufactured by Sekisui Specialty Chemicals, trade name "SELVOL103”) is used, and the type and amount of compound (A) are as shown in Tables 3 and 4. It was carried out in the same manner as in Example 1 except that it was changed to
• the laminate strength of the laminate packaging material obtained in each example and comparative example was measured in accordance with JIS-K-7127. Specifically, the laminate packaging material is cut into strips with a width of 15 mm, and the polyamide film (base material) on which the coating film is formed is subjected to a tensile tester "Tensilon" under a room temperature environment (23 ° C.), LLDPE film. (Heat-seal layer) was peeled off at a speed of 200 mm/min with a T-shape to measure the lamination strength (N/15 mm).
• test pouch obtained in each example and comparative example was compared with a blank to evaluate yellowing by visual observation. After that, it was left at room temperature for 4 weeks, and the appearance after the standing was observed.
• C More yellowing or browning occurred than the blank, and the appearance was at a level that could not be used practically.

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