JP2005187590A - Adhesive composition - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To obtain an adhesive for bonding impregnated paper. <P>SOLUTION: The adhesive composition comprises a copolymer composed of a carboxy group-containing monomer (A) and a monomer (B) copolymerizable with the monomer and a polyamide-based resin. The copolymer has -40 to +5°C glass transition temperature and 1.5-60 mg KOH/g acid value. The amount of the polyamide-based resin is 0.1-15 parts wt based on 100 parts wt. of the copolymer. <P>COPYRIGHT: (C)2005,JPO&NCIPI

Description

  The present invention relates to an adhesive composition.

Vinyl acetate-based resin emulsions have been used for a long time as adhesives for paper, but their water-resistant adhesiveness is not sufficient, and improvements have been studied for a long time.
Examples of such adhesives that have been studied for improvement include an adhesive obtained by adding polyamide epichlorohydrin or the like to a copolymer emulsion composed of a predetermined vinyl acetate-carboxyl group-containing monomer, and a predetermined modified polyvinyl alcohol. An adhesive composed of an aqueous emulsion containing a polymer of an ethylenically unsaturated monomer as a dispersant and a polyamide resin (see Patent Document 2), a predetermined carboxyl group-modified polyvinyl alcohol aqueous solution and a polyamide epoxy resin There are known adhesives (see Patent Document 3) and the like.

Japanese Patent No. 3065243 Japanese Patent Laid-Open No. 7-18516 JP 2001-3022 A

  However, any of the above-described adhesives has a problem that it is difficult to bond impregnated paper obtained by impregnating paper with resin, and it cannot be used when the impregnated paper is a target.

  Accordingly, an object of the present invention is to provide an adhesive capable of bonding impregnated paper.

  The present invention comprises a copolymer comprising a monomer (A) containing a carboxyl group and a monomer (B) copolymerizable therewith, and a polyamide-based resin. The glass transition temperature is -40 to 5 ° C., the acid value is 1.5 to 60 mg KOH / g, and the content of the polyamide-based resin with respect to 100 parts by weight of the copolymer is 0.1 to 15 weights. By using the adhesive composition which is a part, the above-mentioned problems have been solved.

  Since a specific copolymer is used, it is possible to bond an impregnated paper that is excellent in low-temperature adhesiveness and impregnated with a resin or the like.

The adhesive composition according to the present invention comprises a predetermined monomer (hereinafter referred to as “monomer (A)”) and a monomer copolymerizable therewith (hereinafter referred to as “monomer (B)”. And a polyamide-based resin.
The monomer (A) refers to a monomer containing a carboxyl group, and examples thereof include acrylic acid, methacrylic acid and (anhydrous) maleic acid.
The monomer (B) is a monomer copolymerizable with the monomer (A), and examples thereof include olefins, fatty acid vinyl esters, and (meth) acrylic monomers.

Examples of the olefin include ethylene and propylene.
Examples of the fatty acid vinyl ester include vinyl formate, vinyl acetate, vinyl propionate, vinyl butyrate, vinyl caproate, vinyl caprylate, vinyl laurate, vinyl versatate (trade name: Veova 10, manufactured by Shell Japan) Etc. 1-14 are preferable and, as for carbon number of the fatty acid part of this fatty acid vinyl ester, the thing of 2-12 is more preferable. When the number of carbon atoms in the fatty acid portion is greater than 14, the polymerization stability may be poor, unreacted monomers may remain, or the stability of the dispersion over time may be insufficient.

  As said (meth) acrylic-type monomer, the C3-C10 thing of an alkyl group is good, and the thing of 4-8 is more preferable. When the alkyl group has less than 3 carbon atoms, the water resistance of the resulting adhesive tends to deteriorate. On the other hand, when the carbon number of the alkyl group is larger than 10, the polymerization stability is poor, and unreacted monomers remain, and the dispersion with time tends to be insufficient.

  Specific examples of the (meth) acrylic monomer include butyl (meth) acrylate, amyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, isooctyl (meth) acrylate, and (meth) acrylic acid. n-octyl, n-nonyl (meth) acrylate, isononyl (meth) acrylate, decyl (meth) acrylate, lauryl (meth) acrylate, hydroxyethyl (meth) acrylate, methoxyethyl (meth) acrylate, etc. As an example, (meth) acrylic acid ester can be given. These may use only one monomer or may use two or more plural monomers in combination. In the present invention, “(meth) acryl” means “acryl or methacryl”.

  Among the monomers (B), at least one monomer selected from the group consisting of (meth) acrylic monomers, (meth) acrylic monomers and vinyl acetate, and vinyl acetate and ethylene, Use of a monomer group is more preferable from the viewpoint of polymerization stability.

  Said monomer (A) and monomer (B) can obtain the said copolymer by carrying out emulsion polymerization by arbitrary methods. The content ratio of the monomer (A) to the total amount of the monomer (A) and the monomer (B) constituting the copolymer is preferably 0.1 to 10% by weight, and 0.3 to 7 Weight percent is more preferred. When the content ratio of the monomer (A) is less than 0.1% by weight, the adhesion to the impregnated paper tends to deteriorate. On the other hand, when it is more than 10% by weight, the polymerization stability may be lowered.

  In the above emulsion polymerization, polymerization can be carried out using general conditions, that is, conditions such as normally used temperature and pressure, a polymerization catalyst, a protective colloid agent, an emulsifier and the like.

  Examples of the protective colloid agent include partially saponified or completely saponified polyvinyl alcohol (hereinafter abbreviated as “PVA”), ethylene-vinyl acetate copolymer partial (or complete) saponified product, hydroxyalkyl cellulose, etc. Cellulose derivatives, polyacrylic acid derivatives, natural water-soluble polymers such as starch and gelatin can be used. As the emulsifier, a surfactant such as polyoxyethylene alkyl ether or polyoxyethylene alkyl phenyl ether can be used. These protective colloid agents and emulsifiers can be used alone or in combination of two or more.

  Of the above PVA, polyvinyl alcohol having a saponification degree of 70 to 99.5%, preferably 85 to 99.5% is preferably used from the viewpoint of polymerization stability and viscosity stability. When the saponification degree is lower than 70%, the polymerization stability tends to be insufficient. On the other hand, although it may be larger than 99.5%, the influence of the crystallinity of polyvinyl acetate is exerted, so that the viscosity stability of the resulting dispersion may be deteriorated and the viscosity change with time may be caused. 0.5% or less is preferable.

  The polymerization degree of the polyvinyl alcohol is preferably from 300 to 3000, and more preferably from 500 to 2700. When it is smaller than 300, the hot-water adhesion of the resulting dispersion tends to be insufficient. On the other hand, when it is larger than 3000, the viscosity of the dispersion increases, and the workability tends to deteriorate.

  The amount of the protective colloid agent or emulsifier used is preferably 3 to 20% by weight and preferably 4 to 15% by weight with respect to the total amount of the component (A) and the component (B). When the content is less than 3% by weight, the polymerization stability is insufficient. On the other hand, when the content is more than 20% by weight, the viscosity of the resulting dispersion is increased, and the hot water adhesion resistance may be deteriorated.

  The glass transition temperature (Tg) of the copolymer obtained by the above method needs to be −40 to + 5 ° C., and preferably −20 to 0 ° C. When it is lower than −40 ° C., the water-resistant adhesion tends to deteriorate. On the other hand, when it is higher than 5 ° C., the low-temperature film-forming property is insufficient, and the adhesiveness of the impregnated paper tends to be insufficient.

  The acid value of the copolymer obtained by the above method can be controlled by the content ratio of the monomer (A), and is 1.5 to 60 mgKOH / g. Among these, 2 to 50 mgKOH / g is preferable, and 3 to 30 mgKOH / g is more preferable. If it is less than 1.5 mgKOH / g, the adhesion to the impregnated paper may be deteriorated. On the other hand, if it is larger than 60 mgKOH / g, the stability during polymerization tends to be low, and a good dispersion tends to be difficult to obtain. The acid value can be measured according to the method described in JIS K 2501.

The polyamide-based resin refers to a resin having an amide bond, and examples thereof include nylon resins such as nylon 66 and nylon 6, polyamide epoxy resins, and the like.
Examples of the polyamide epoxy resin include resins obtained by reacting polyamine polyamides with epihalohydrin.

  Examples of the polyamine polyamides include polycondensates of dicarboxylic acids and polyalkylene polyamines. Examples of dicarboxylic acids used in the polyamine polyamides include aliphatic dicarboxylic acids such as malonic acid, succinic acid, glutaric acid, adipic acid, and sebacic acid, and aromatic dicarboxylic acids such as phthalic acid, isophthalic acid, and terephthalic acid. Dicarboxylic acids such as sodium salts and potassium salts of these dicarboxylic acids, dicarboxylic acid esters such as diethyl malonate and dimethyl adipate; and dicarboxylic acid anhydrides such as succinic anhydride and glutaric anhydride.

  Among the dicarboxylic acids, aliphatic dicarboxylic acids having about 3 to 10 carbon atoms are preferable, and adipic acid is more preferable. Only one kind of the above dicarboxylic acids may be used, or two or more different dicarboxylic acids may be mixed and used.

Examples of the polyalkylene polyamines include diethylenetriamine, triethylenetetramine, tetraethylenepentamine, iminobispropylamine, 3-azahexane-1,6-diamine, 4,7-diazadecane-1,10-diamine, and the like. It is done.
Among the polyalkylene polyamines, diethylenetriamine and triethylenetetramine are more preferable. Only one kind of the above polyalkylene polyamines may be used, or two or more different polyalkylene polyamines may be mixed and used.

  In the polycondensation reaction to give the polyamine polyamides, it is preferable to use 0.9 to 1.4 equivalents of dicarboxylic acid with respect to 1 equivalent of the primary amino group (terminal amino group) of the polyalkylene polyamine. It is preferable to use 9 to 1.2 equivalents. In this polycondensation reaction, aminocarboxylic acids and diamines may be used in combination.

  Examples of the aminocarboxylic acids include aminocarboxylic acids such as glycine, alanine and aminocaproic acid and esters thereof, and lactams such as caprolactam. Examples of the diamines include ethylenediamine, 1,3-propanediamine, 1,4-butanediamine, 1,6-hexanediamine, and the like.

  Examples of the polycondensation reaction include a method of removing generated water or alcohol out of the system at a reaction temperature of about 50 to 250 ° C. under normal pressure or reduced pressure. The reaction is performed until the viscosity of the 50% aqueous solution of the reaction product is about 100 mPa · s or more, preferably about 400 mPa · s to 1000 mPa · s.

  In the polycondensation reaction, mineral acids and sulfonic acids can be used as catalysts. Examples of the mineral acid include hydrochloric acid, sulfuric acid, nitric acid, phosphoric acid and the like, and specific examples of the sulfonic acids include benzenesulfonic acid and paratoluenesulfonic acid. Among the above catalysts, sulfuric acid or sulfonic acids are more preferable.

  The amount of the catalyst used is usually about 0.005 to 0.1 mol, preferably 0.01 to 0.05 mol, per 1 mol of polyalkylene polyamine.

  The adhesive composition according to the present invention can be obtained by mixing the copolymer and the polyamide resin. When the copolymer is a polymer obtained by emulsion polymerization with an aqueous medium such as water, the liquid is an aqueous emulsion. And when this is mixed with the said polyamide-type resin, the liquid form of the adhesive composition obtained will turn into a water-system emulsion.

  As for content of the said polyamide-type resin with respect to 100 weight part of said copolymers, 0.1-15 weight part is used and 0.5-10 weight part is preferable. When the amount is less than 0.1 part by weight, the adhesion to the impregnated paper tends to deteriorate. On the other hand, when it is more than 15 parts by weight, the water-resistant adhesion tends to be inferior.

  The adhesive composition according to the present invention can contain other components as long as the effects of the present invention are not impaired.

  The viscosity of the adhesive composition thus obtained is usually preferably 1000 to 20000 mPa · s (25 ° C.) and preferably 2000 to 15000 mPa · s (25 ° C.) as an aqueous dispersion having a solid content of 40 to 60% by weight. ) Is more preferable. If it is lower than 1000 mPa · s, it may sag or flow when the adhesive is applied. On the other hand, when it is higher than 20000 mPa · s, workability during application tends to deteriorate.

  The adhesive composition of the present invention exhibits excellent adhesion to impregnated paper impregnated with resins such as rubbers, phenolic resins and acrylic resins to improve dimensional stability and durability. Among them, it is effective for adhesion of impregnated paper for decorative paper overlay impregnated with styrene rubber, acrylic resin or the like.

The adhesive composition according to the present invention can be used as a one-pack type, and is easier to handle than the two-pack type.
Moreover, the adhesive composition according to the present invention does not require the use of a low-boiling organic compound component. For this reason, in addition to various paper products such as decorative paper, it can be used for wood products such as plywood, medium-quality fiberboard, and wood-based decorative boards such as particle board. Paper products using this adhesive composition And wood products do not contain formaldehyde or low boilers. For this reason, the building using this can prevent generation | occurrence | production of the volatile organic compound (VOCs) considered to be one of the causes of the occurrence of sick house syndrome.

  EXAMPLES Hereinafter, although this invention is demonstrated in detail using an Example, this invention is not limited by a following example, unless the summary is exceeded. First, tests and evaluation methods performed in Examples and Comparative Examples and raw materials used will be described.

[Test and evaluation method]
<Viscosity>
Using a rotational viscometer (B type viscometer, manufactured by Toki Sangyo Co., Ltd., BH type, TV-10 type viscometer) specified in JIS K 7117, at a temperature of 25 ° C., No. 10 The measurement was performed under conditions of 3, 4, 5 rotor (selected according to viscosity).

<Nonvolatile content>
In accordance with JIS K 6828-1996 (Test method for synthetic resin emulsion), an aluminum foil dish having a diameter of about 40 mm was used, and the drying time in a thermostatic bath was 180 ± 5 minutes. Was measured.

<Glass transition temperature>
The glass transition temperature of the copolymer was determined from the glass transition temperature of the monomer homopolymer according to the FOX equation. (For the formula of FOX, refer to Emulsion Latex Handbook, Taiseisha Co., Ltd., pages 280-281.)

<Acid value>
The copolymer was measured according to the method described in JIS K 2501.

<MFT>
Using a thermal gradient tester (manufactured by Nichi Shoji Co., Ltd.), the film forming temperature of the aqueous emulsion was measured according to ASTM D2354-65T.

<Adhesion resistance>
MDF (manufactured by Hokushin Co., Ltd., Starwood) as a base material, impregnated paper (manufactured by Toppan Printing Co., Ltd .: Cynthia Neo), or pre-coated paper (manufactured by Chiyoda Gravure Co., Ltd .: gloss mat TS-12) , The substrate was coated with an aqueous emulsion in a solid form so as to be 60 g / m ² , an adherend was placed on the substrate, and a load of 0.005 N / mm ² was applied for 16 hours, A decorative board was prepared by curing at room temperature for 72 hours. This decorative board is cut into a size of 75 mm × 75 mm, and tested according to Japanese Agricultural Standards: Special plywood type 2 immersion test (2 hours immersion in 70 ° C. warm water and 3 hours drying at 60 ° C.). Judged by criteria.
-The length of the non-peeled portion in the same adhesive layer is 50 mm or more on any side surface.
-X ... The length of the part which has not peeled in the same adhesion layer is less than 50 mm in any one or more side surfaces.

<Compounding stability>
The state of the aqueous emulsion after observing one day after blending the copolymer and the polyamide resin was observed and evaluated according to the following criteria.
・ ○… No abnormality ・ △… Thickening was observed ・ ×… Gel was formed

[Raw materials used]
Vinyl acetate: manufactured by Nippon Synthetic Chemical Co., Ltd. (hereinafter abbreviated as “VAC”)
-2-ethylhexyl acrylate: manufactured by Mitsubishi Chemical Corporation (hereinafter abbreviated as “2EHA”)
・ Butyl acrylate: manufactured by Mitsubishi Chemical Corporation (hereinafter abbreviated as “BA”)
Acrylic acid: manufactured by Mitsubishi Chemical Corporation (hereinafter abbreviated as “AA”)
・ Ethylene ... Mitsubishi Chemical Corporation (hereinafter abbreviated as “ET”)

Polyvinyl alcohol: manufactured by Nippon Synthetic Chemical Industry Co., Ltd .: Gohsenol AH-17 (saponification degree 98%, polymerization degree 1700, hereinafter abbreviated as “AH17”)
Polyvinyl alcohol: manufactured by Nippon Synthetic Chemical Industry Co., Ltd .: Gohsenol GH-17 (saponification degree 88%, polymerization degree 1700, hereinafter abbreviated as “GH17”)

Modified polyvinyl alcohol: manufactured by Nippon Synthetic Chemical Industry Co., Ltd .: Gohsenal T330H (15% carboxylic acid modification, saponification degree 98%, polymerization degree 1700, hereinafter abbreviated as “T330H”)
・ Polyamide resin: Toho Chemical Industries, Ltd .: Sparamin 30 (polyamide epoxy resin, 30% aqueous solution)

・ Polymerization initiator: 35% hydrogen peroxide solution (Mitsubishi Gas Chemical Co., Ltd.)
・ Reducing agent: Tartaric acid (manufactured by Fuso Chemical Industry Co., Ltd.)

(Examples 1-5, Comparative Examples 1-6)
A 10% aqueous solution of AH17, GH17, or T330H as a protective colloid agent, and water were introduced into a flask equipped with a stirrer, a reflux condenser, and a raw material inlet, in amounts (solid) shown in Table 1, 70 ° C. The temperature was raised to. Thereafter, water is added to 1 g of the polymerization initiator and 0.3 g of the reducing agent to make a total amount of 10 g, and a mixed solution of the monomer and the amount shown in Table 1 is dropped simultaneously over 6 hours to perform emulsion polymerization. And cooled to obtain a copolymer dispersion.
An aqueous emulsion was obtained by adding the amount of polyamide resin shown in Table 1 to the obtained copolymer dispersion. The above test and evaluation were performed using the obtained aqueous emulsion. The results are shown in Table 1.
In Comparative Example 5, the obtained aqueous emulsion was gelled, and thus the above test and evaluation were not performed.

Claims (7)

A copolymer comprising a monomer (A) containing a carboxyl group and a monomer (B) copolymerizable therewith, and a polyamide-based resin;
The glass transition temperature of the copolymer is −40 to + 5 ° C., and the acid value is 1.5 to 60 mgKOH / g,
Content of the said polyamide-type resin with respect to 100 weight part of said copolymers is 0.1-15 weight part adhesive composition.   The content ratio of the monomer (A) to the total amount of the monomer (A) and the monomer (B) constituting the copolymer is 0.1 to 10% by weight. Adhesive composition.   The adhesive composition according to claim 1, wherein the monomer (A) is acrylic acid or methacrylic acid.   The monomer (B) is at least one monomer selected from the group consisting of (meth) acrylic monomers, (meth) acrylic monomers and vinyl acetate, and vinyl acetate and ethylene. The adhesive composition according to any one of claims 1 to 3, which is a mass group.   The adhesive composition according to claim 4, wherein the (meth) acrylic monomer is a (meth) acrylic acid ester having an alkyl group having 4 to 10 carbon atoms.   The adhesive composition according to any one of claims 1 to 5, wherein the polyamide-based resin is a polyamide epoxy resin.   The adhesive composition according to any one of claims 1 to 6, which is an aqueous emulsion having a viscosity of 1000 to 20000 mPa · s.