JP4184284B2 - Reactive hot melt adhesive - Google Patents

Description

  The present invention relates to a reactive hot melt adhesive. More specifically, the present invention relates to a hot melt adhesive suitably used for manufacturing construction members (floor materials, panels, boards, cloths, plastics, rubber, metals, etc.) and clothing members (fibers, woven fabrics, films, etc.).

Hot melt adhesives are solid and solvent-free at room temperature, and are easy to use and useful, such as being usable only with a heating operation. Reactive hot melt adhesives have attracted attention in recent years as further improved in heat resistance and adhesiveness.
Conventionally, as a reactive hot melt adhesive, one made of a polyester-based or polyether-based urethane prepolymer and a low molecular weight xylene resin is known (for example, Patent Document 1).
Japanese Patent No. 2651640

However, although this reactive hot melt adhesive is excellent in the length of time that can be adhered after application and the elasticity after curing, the initial adhesive force immediately after application is expressed mainly by tackiness. In addition, because the resin strength is weak both before and after curing, the adherend may float and peel before it is completely cured when bonding adherends with distortion (such as construction members). It was. In addition, due to the high polarity of xylene resin, adhesion to low adherends (for example, olefin resins such as polypropylene and polyethylene) is weak and causes breakage at the interface even after curing and has sufficient adhesive strength. There were problems such as being unable to obtain. Furthermore, for applications in which the bonded body is cut after curing (adhesion of construction members and clothing members), resin cutting occurs during cutting, and the curing time until cutting is 1 week. This required the problem of poor production efficiency. In addition, the low molecular weight xylene resin is partly decomposed when it is exposed to a high temperature of 120 ° C. or more, generating odors and smoke, and thus has a problem in terms of working environment.
The purpose of the present invention is to maintain the length of time for which adhesion is possible after coating, while preventing the distorted adherend from floating and peeling, and to ensure the adhesion to the adherend with low polarity. Is to provide a reactive hot melt adhesive that is short and does not contaminate the work environment.

The inventor of the present invention has arrived at the present invention as a result of intensive studies to solve the above problems.
That is, the present invention provides a polyisocyanate (A), a polyolefin-based polyol (B), Rosin having an active hydrogen which react with isocyanates (C), and Ri Na ethylenically unsaturated monomer is polymerized comprising been obtained polymer polyol (D) is obtained by reacting in a polyol, [ The equivalent ratio of (B), (C), (D) in total OH (hydroxyl group) / [(A) NCO (isocyanate group)] is 1 / 1.01 to 1/5, and [(B) the weight ratio of + (C)] / (D) is a 100 / (100-500) der Ru reactive hot-melt adhesive.

The reactive hot melt adhesive of the present invention has the following effects.
Compared to conventional hot melt adhesives composed of polyester or polyether urethane prepolymers and low molecular weight xylene resins, it has better adhesion when applied to adherends with low polarity and pollutes the work environment. In addition, it is possible to prevent floating and peeling after bonding of a distorted adherend and shorten the curing time until cutting of the bonded body.

In the present invention, the polyisocyanate (A) is an aromatic polyisocyanate having 6 to 20 carbon atoms (excluding carbon in the NCO group, the same shall apply hereinafter), an aliphatic polyisocyanate having 2 to 18 carbon atoms, or 4 to 15 carbon atoms. Alicyclic polyisocyanates, araliphatic polyisocyanates having 8 to 15 carbon atoms, modified products of these polyisocyanates, and mixtures of two or more of these.
Specific examples of the aromatic polyisocyanate include 1,3- and / or 1,4-phenylene diisocyanate, 2,4- and / or 2,6-tolylene diisocyanate (TDI), crude TDI, and 2,4′-. And / or 4,4′-diphenylmethane diisocyanate (MDI), 4,4′-diisocyanatobiphenyl, 3,3′-dimethyl-4,4′-diisocyanatobiphenyl, 3,3′-dimethyl-4, Examples include 4'-diisocyanatodiphenylmethane, crude MDI, 1,5-naphthylene diisocyanate, 4,4 ', 4 "-triphenylmethane triisocyanate, m- and p-isocyanatophenylsulfonyl isocyanate.

Specific examples of the aliphatic polyisocyanate include ethylene diisocyanate, tetramethylene diisocyanate, hexamethylene diisocyanate (HDI), dodecamethylene diisocyanate, 1,6,11-undecane triisocyanate, 2,2,4-trimethylhexamethylene diisocyanate, and lysine. Diisocyanate, 2,6-diisocyanatomethylcaproate, bis (2-isocyanatoethyl) fumarate, bis (2-isocyanatoethyl) carbonate, 2-isocyanatoethyl-2,6-diisocyanatohexanoate, etc. Is mentioned.
Specific examples of the alicyclic polyisocyanate include isophorone diisocyanate (IPDI), dicyclohexylmethane-4,4′-diisocyanate (hydrogenated MDI), cyclohexylene diisocyanate, methylcyclohexylene diisocyanate (hydrogenated TDI), bis (2- And isocyanatoethyl) -4-cyclohexene-1,2-dicarboxylate, 2,5- and / or 2,6-norbornane diisocyanate.

Specific examples of the araliphatic polyisocyanate include m- and / or p-xylylene diisocyanate (XDI), α, α, α ′, α′-tetramethylxylylene diisocyanate (TMXDI), and the like.
The modified polyisocyanates include modified MDI (carbodiimide-modified MDI, trihydrocarbyl phosphate-modified MDI), biuret-modified HDI, isocyanurate-modified HDI, isocyanurate-modified IPDI, and the like. Combination with the above mixture] is included.
Among these, HDI, IPDI, TDI, MDI, XDI and TMXDI are preferable, and HDI, MDI and XDI are particularly preferable.

The number average molecular weight can be measured by the gel permeation chromatography method (GPC method) under the following conditions.
Solvent: Tetrahydrofuran reference material: Polyethylene glycol (PEG)
Sample concentration: 0.25 wt / vol%
Column temperature: 23 ° C

In the present invention, examples of the polyolefin-based polyol (B) include polyols obtained by polymerizing olefins and having an active hydrogen group at the terminal.
Specific examples of (B) include polybutadiene polyol, polyisoprene polyol, hydrogenated polybutadiene polyol, and hydrogenated polyisoprene polyol.
Of these, polybutadiene polyol and hydrogenated polybutadiene polyol are preferable, and polybutadiene polyol is more preferable.
Examples of rosins (C) having active hydrogen capable of reacting with isocyanate include wood rosin, gum rosin, hydrogenated rosin, disproportionated rosin, tall oil rosin, wood polymerized rosin, gum polymerized rosin, and tall oil Polymerized rosin such as polymerized rosin, and mixtures thereof. Moreover, it is preferable to use rosins having a hydroxyl group as the rosins. For example, there are polyester polyols or polyether polyols having a rosin skeleton, which can be obtained by reacting with polyols using rosins as the acid component of the polyester, or compounds having glycidyl groups in the molecule and rosins. It can be obtained by reaction. The amount of hydroxyl groups is preferably 1 to 5 in one molecule.
The above rosins are preferred because they can react with (A) to form a urethane prepolymer.

Examples of the polymer polyol (D) in the present invention include a polymer polyol obtained by polymerizing an ethylenically unsaturated monomer in the polyol (d).
The polyol (d) is preferably one or more selected from the following (d1) and (d2).
(D1): Phenols or alcohols added with an alkylene oxide having 2 to 4 carbon atoms (d2): Condensed polyester polyol of dicarboxylic acids and (d1) Among these, (d1) is preferred.

  Specific examples of phenols (d11) include dihydric phenols having 6 to 30 carbon atoms such as catechol, resorcinol, hydroquinone, dihydroxymethylbenzene, bisphenol A, bisphenol F, bisphenol S, dihydroxydiphenyl ether, dihydroxydiphenyl. Examples thereof include thioether, binaphthol, and alkyls (having 1 to 10 carbon atoms) or halogen substituents thereof. Bisphenol A and bisphenol F are preferable.

  Specific examples of the alcohol (d12) are preferably divalent or higher alcohols having 2 to 20 carbon atoms, such as dihydric alcohols (ethylene glycol, diethylene glycol, propylene glycol, dipropylene glycol, 1,4-butanediol, Neopentyl glycol, 1,6-hexanediol, 1,8-octamethylenediol, alkyl dialkanolamine, etc.), low molecular diols having a cyclic group [1,4-bis (hydroxymethyl) cyclohexane, m- and p -Xylylene glycol, 1,4-bis (2-hydroxyethoxy) benzene, 1,4-bis (α-hydroxyisopropyl) benzene, 2,2-bis (4-hydroxyethoxyphenyl) propane, etc.], trihydric alcohol (Glycerin, trimethylolpropane, hex Ntorioru etc.), tetrafunctional or higher polyhydric alcohols (sorbitol, shoe - closed, etc.). More preferred are dihydric alcohols and trihydric alcohols.

Examples of the alkylene oxide (d13) include alkylene oxides having 2 to 4 carbon atoms such as ethylene oxide, propylene oxide, 1,2-, 1,3-, 2,3-, or 1,4-butylene oxide, and these 2 More than one type of combined system [block addition (chip type, balance type, active secondary type, etc.), random addition, or a mixed system thereof] can be mentioned. Of these, ethylene oxide and propylene oxide are preferred.
The number of added moles of (d13) is preferably 1 to 100 moles, more preferably 2 to 50 moles.
The addition of the alkylene oxide can be carried out by a known method, in the absence of a catalyst, or in the presence of a catalyst (an alkali catalyst, an amine catalyst, an acidic catalyst) (especially in the latter half of the addition), at atmospheric pressure or at an applied The reduction is performed in one stage or in multiple stages.

The dicarboxylic acid (d14) constituting the condensed polyester polyol is preferably a dicarboxylic acid having 2 to 20 carbon atoms, and examples thereof include aliphatic dicarboxylic acids, aromatic dicarboxylic acids, and alicyclic dicarboxylic acids.
Examples of the aliphatic dicarboxylic acid include oxalic acid, malonic acid, succinic acid, glutaric acid, methyl succinic acid, dimethyl malonic acid, β-methyl glutaric acid, ethyl succinic acid, isopropyl malonic acid, adipic acid, pimelic acid, suberic acid, Examples include azelaic acid, sebacic acid, undecanedicarboxylic acid, dodecanedicarboxylic acid, tridecanedicarboxylic acid, tetradecanedicarboxylic acid, and icosanedicarboxylic acid.

Examples of the aromatic dicarboxylic acid include terephthalic acid, isophthalic acid, phthalic acid, phenylmalonic acid, homophthalic acid, phenylsuccinic acid, β-phenylglutaric acid, α-phenyladipic acid, β-phenyladipic acid, and biphenyl-2. 2,2'-dicarboxylic acid, biphenyl-4,4'-dicarboxylic acid, naphthalenedicarboxylic acid and the like.
Examples of the alicyclic dicarboxylic acid include 1,3-cyclopentanedicarboxylic acid, 1,2-cyclopentanedicarboxylic acid, 1,4-cyclohexanedicarboxylic acid, 1,2-cyclohexanedicarboxylic acid, and 1,4-cyclohexanedicarboxylic acid. Examples include acetic acid, 1,3-cyclohexanediacetic acid, 1,2-cyclohexanediacetic acid and the like.
Of these, aliphatic dicarboxylic acids and aromatic dicarboxylic acids are preferable, and succinic acid, adipic acid, terephthalic acid, and phthalic acid are more preferable.

  The molar ratio of (d1) and dicarboxylic acids (d14) is preferably 101/100 to 2/1, and more preferably 51/50 to 3/2. The esterification reaction may be non-catalyzed or may use an esterification catalyst. Examples of the esterification catalyst include protonic acids such as phosphoric acid, alkali metals, alkaline earth metals, transition metals, 2B metals, 4B metals, and 5B metals having 2 to 4 carbon carboxylates, carbonates, sulfates, Examples include phosphates, oxides, chlorides, hydroxides, and alkoxides. Among these, antimony trioxide, monobutyltin oxide, tetrabutyl titanate, tetrabutyl zirconate, zirconyl acetate, zinc acetate and the like are preferable from the viewpoint of the color tone of the product. The amount of the esterification catalyst used is not particularly limited as long as a desired molecular weight can be obtained. However, from the viewpoint of reactivity and color tone, the amount of esterification catalyst is 0. 005-5 mass% is preferable, More preferably, it is 0.1-1.0 mass%.

The esterification reaction is performed in the presence of an inert gas such as nitrogen or under reduced pressure (for example, 133 Pa or less). In order to accelerate the reaction, an organic solvent can be added and refluxed. After completion of the reaction, the organic solvent is removed. The organic solvent is not particularly limited as long as it has no active hydrogen such as a hydroxyl group. For example, hydrocarbon solvents such as toluene and xylene; ketone solvents such as methyl ethyl ketone and methyl isobutyl ketone; ethyl acetate, An ester solvent such as butyl acetate can be used.
The reaction temperature is usually 120 to 250 ° C, preferably 150 to 230 ° C. The reaction time is usually 1 to 40 hours, preferably 3 to 24 hours.
The end point of the reaction can be measured by acid value (AV). The acid value at the end point is preferably 3 or less, more preferably 2 or less. The number average molecular weight (Mn) of the obtained condensed polyester polyol is preferably 500 to 20,000, more preferably 800 to 10,000. Mn is a value measured by the GPC method.

Examples of the ethylenically unsaturated monomer include α-olefins having 3 to 30 carbon atoms (hexene, octene, decene, dodecene, tetradecene, hexadecene, octadecene, aicosene, heneicosene, docosene, tricosene, tetracosene, pentacosene, hexacosene. Etc.), C8-C15 aromatic hydrocarbon monomers (styrene, α-methylstyrene, etc.), unsaturated nitriles [(meth) acrylonitrile, etc.], (meth) acrylic acid esters {(meth) Acrylic acid alkyl ester (alkyl group having 1 to 30 carbon atoms) [methyl (meth) acrylate, ethyl (meth) acrylate, butyl (meth) acrylate, nonyl (meth) acrylate, decyl (meth) acrylate, undecyl (meth) Acrylate, dodecyl (meth) acrylate, tridecyl ( Acrylate), tetradecyl (meth) acrylate, pentadecyl (meth) acrylate, hexadecyl (meth) acrylate, octadecyl (meth) acrylate, eicosyl (meth) acrylate, docosyl (meth) acrylate, etc.], (meth) acrylic acid hydroxyalkyl ester [Hydroxyethyl (meth) acrylate, hydroxypropyl (meth) acrylate, etc.]}, ethylenically unsaturated carboxylic acid and its derivatives [(meth) acrylic acid, (meth) acrylamide, etc.], aliphatic hydrocarbon monomer (ethylene , Propylene, etc.), fluorine-containing vinyl monomers [perfluorooctylethyl (meth) acrylate, etc.], nitrogen-containing vinyl monomers (diaminoethyl methacrylate, morpholinoethyl methacrylate, etc.), glycidyl (meth) acrylate Relay - door, and the like.
Of these, preferred are aromatic hydrocarbon monomers, unsaturated nitriles [(meth) acrylonitrile, etc.] and (meth) acrylic acid esters, and more preferred are styrene, (meth) acrylonitrile, ( It is a (meth) acrylic acid alkyl ester.

  The content of the ethylenically unsaturated monomer constituting the polymer polyol is preferably 0.1 to 90% by weight, more preferably 5 to 80% by weight, particularly preferably 10%, based on the polymer polyol. ~ 70 wt%. The average functional group number of the polymer polyol is preferably 2 to 8, and more preferably 2 to 4. The number average molecular weight of the polymer polyol is preferably 300 to 30,000, more preferably 500 to 20,000. The number average molecular weight is a value measured by the GPC method.

  As a method for producing a polymer polyol, for example, a method of polymerizing an ethylenically unsaturated monomer in a polyol in the presence of a polymerization initiator (radical generator, etc.) (Japanese Patent Publication No. 39-24737, Japanese Patent Publication No. 47- No. 47999, Japanese Patent Laid-Open No. 50-15894, etc.).

(B), (C), and (D) may contain a polyol (d) constituting (D), if necessary. (D) at this time may be the same as the polyol constituting (D), or may be a different type of polyol.
The equivalent ratio of [(B), (C), (D) and, if necessary, the total OH (hydroxyl group) of (d)] / [NCO (isocyanate group) of (A)] is preferably 1/1. 0.01 to 1/5, more preferably 1 / 1.2 to 1/4, and particularly preferably 1 / 1.5-1 to 1/3. When the isocyanate group of (A) is made excessive, it becomes an NCO-terminated urethane prepolymer and has reactivity when used as a hot melt adhesive.
4 The blending ratio of each of the above (B) and (C) is preferably 1 to 90% by weight of (B) and 10 to 99 of (C) with respect to the total weight of (B) and (C). % By weight, more preferably 1 to 80% by weight of (B) and 20 to 99% by weight of (C). When (B) is 90% by weight or less, the obtained adhesive has good thermal stability, and when it is 1% by weight or more, the adhesive strength of the obtained adhesive with an olefin resin is improved. When (C) is 99% by weight or less, the viscosity of the obtained adhesive is lowered, and when it is 10% by weight or more, the initial adhesive force of the obtained adhesive is further improved.
The ratio (weight ratio) of (B) + (C) / (D) is preferably 100/0 to 500, and more preferably 100/50 to 400. By adding (D), the adhesive strength is further improved, and when it is 500 or less, the initial adhesive strength of the obtained adhesive is improved.

The manufacturing method of a urethane prepolymer is not specifically limited, The following two types of methods can be illustrated.
(I) A method in which (A) and (B) and (A) and (C) are individually reacted and then kneaded.
(Ii) A method in which a mixture of (B) and (C) is reacted with (A).
Of the above methods, the method (ii) is preferred from the viewpoint of the simplicity of the production process and the thermal stability of the resulting adhesive.

When the urethane prepolymer is produced, a urethanization catalyst may be used. As the urethanization catalyst, those conventionally used for polyurethane production can be used.
Metal catalysts such as tin catalysts [trimethyltin laurate, trimethyltin hydroxide, dimethyltin dilaurate, dibutyltin diacetate, dibutyltin dilaurate, stannous octoate, dibutyltin maleate, etc.], lead catalysts [lead oleate, 2-ethylhexanoate, lead naphthenate, lead octenoate, etc.], other metal catalysts [naphthalic acid metal salts such as cobalt naphthenate, phenylmercury propionate, etc.]; and amine catalysts such as triethylenediamine, tetramethyl Ethylenediamine, diazabicycloalkenes [1,8-diazabicyclo [5,4,0] undecene-7 [DBU (manufactured by San Apro, registered trademark)], etc.]; dialkylaminoalkylamines [dimethylaminoethylamine, dimethylaminopropyl Amines, Ethylaminopropylamine, dipropylaminopropylamine, etc.] or heterocyclic aminoalkylamines [2- (1-aziridinyl) ethylamine, 4- (1-piperidinyl) -2-hexylamine, etc.] carbonates and organic acids Salts (such as formate salts) and the like; N-methylmorpholine, N-ethylmorpholine, triethylamine, diethylethanolamine, dimethylethanolamine, and the like; and combinations of two or more of these.

The use amount of the urethanization catalyst is preferably 1% by weight or less, more preferably 0.05% by weight or less, and particularly preferably 0.01% by weight based on the total weight of (A) to (C) if necessary (D). % By weight or less. When it is 1% by weight or less, the thermal stability of the finally obtained adhesive is not impaired.
As reaction conditions, for example, (A) to (C) and a urethanization catalyst are charged into a reaction vessel having a temperature control function, and continuously reacted at a temperature of 50 to 200 ° C. for 30 to 1,000 minutes. Examples thereof include a method, a method in which (A) to (C) and a urethanization catalyst are poured into, for example, a biaxial excluder, and preferably reacted continuously at a temperature of 100 to 220 ° C.
The content of the isocyanate group in the urethane prepolymer comprising (A) to (C) is preferably 0.2 to 10% by weight, more preferably 0.5 to 5% by weight. When it is 0.2% by weight or more, the heat resistance is good, and when it is 10% by weight or less, the thermal stability at the time of heating and melting is good. The number average molecular weight (Mn) of the urethane prepolymer is preferably 500 to 15,000, more preferably 1,000 to 8,000.
Mn is a value measured by a gel permeation chromatography method (GPC method).

The hot melt adhesive of the present invention can contain a tackifying resin (E) that does not contain an active hydrogen such as a hydroxyl group for the purpose of improving the initial adhesive force in the production process or at any stage after production.
As tackifying resin (E), what is generally used for a hot-melt-adhesive can be used, For example, petroleum resin, a styrene resin, a terpene resin, a coumarone resin, etc. are mentioned. The number average molecular weight of these resins is not particularly limited, but is preferably 200 or more and 15,000 or less, more preferably 300 or more and 5,000 or less.
Examples of petroleum resins include aliphatic petroleum resins (polymers based on C4 to C5 mono- or diolefins such as isobutylene, butadiene, 1,3-pentadiene, isoprene, and piperidine), and alicyclic petroleum resins (spent C4). Resin obtained by cyclization and dimerization polymerization of diene component in C5 fraction, resin hydrogenated with aromatic hydrocarbon resin, etc., aromatic petroleum resin (vinyl toluene, indene, α-methylstyrene, C9, etc.) And polymers having a vinyl aromatic hydrocarbon of C10 as a main component), petroleum resins such as aliphatic-aromatic copolymers, and hydrides thereof.

The ring and ball softening point (measurement method: conforming to JAI-7-1991) of (E) is selected depending on the use temperature of the adhesive, but is preferably 30 to 160 ° C, more preferably 60 to 140 ° C.
If a liquid at room temperature is used alone, the cohesive force may be too low, but it can be used in combination with a solid at room temperature.
The addition amount of (E) is preferably 1 to 70% by mass, more preferably 5 to 60% by mass, and particularly preferably 10 to 50% by mass with respect to the entire hot melt adhesive of the present invention. . When the addition amount exceeds 70% by mass, the adhesive strength after curing is insufficient.

In the hot melt adhesive of the present invention, a softening agent can be added for the purpose of adjusting the viscosity, the adhesive strength, the solidification speed, etc. in the production process or at any stage after the production.
Examples of the softening agent include process oil, plasticizer, liquid rubber, and wax. These may be used alone or in combination of two or more. A softener is a liquid or solid at room temperature and melts at the time of use to lower the melt viscosity of a hot melt adhesive, plasticize it to give an adhesive force, or delay or accelerate the solidification rate. is there.
Examples of the process oil include those having a kinematic viscosity (100 ° C.) of 1 to 100 mm ² / s, such as paraffinic oil, naphthenic oil, and aroma oil.
Examples of the plasticizer include those having a weight average molecular weight of 100 to 5,000, such as phthalic acid ester, benzoic acid ester, phosphoric acid ester, aliphatic glycol polyester, and toluenesulfonamide.
Examples of the liquid rubber include those having a weight average molecular weight of 200 to 10,000, such as liquid polybutene, liquid polybutadiene, liquid polyisoprene, and hydrogenated products thereof.
Examples of the wax include those having a weight average molecular weight of 100 to 10,000, such as paraffin wax, microcrystalline wax, Fischer-Tropsch wax, polyethylene wax, polypropylene wax, and oxidized wax obtained by oxidative decomposition thereof, and Examples thereof include acid-modified waxes obtained by graft-modifying unsaturated carboxylic acids (anhydrides) such as (anhydrous) maleic acid, fumaric acid, and (meth) acrylic acid.
The weight average molecular weight is a value measured by the GPC method described above.

Furthermore, the reactive hot melt adhesive of the present invention can be optionally added with other resin additives in the production process or at any stage after production within a range that does not impair the properties of the adhesive according to various purposes and applications. Can be added.
Examples of the additive include pigments (eg, titanium oxide, carbon black, etc.), dyes, fillers (eg, talc, mica, calcium carbonate, etc.), nucleating agents (eg, sorbitol, phosphate metal salt, benzoic acid metal salt, Metal phosphate, etc.), lubricant (eg, calcium stearate, butyl stearate, oleic amide, etc.), mold release agent (eg, carboxyl-modified silicone oil, hydroxyl-modified silicone oil, etc.), antioxidant (eg, phenol-based) Antioxidants, phosphite antioxidants, thioether antioxidants, amine antioxidants, etc., light stabilizers (eg benzotriazole, hindered amine, benzoate, benzotriazole, etc.) and flame retardants (eg halogen series) Flame retardant, phosphorus flame retardant, antimony flame retardant, metal hydroxide -Based flame retardants and the like) and the like.

In the reaction of (D) and (A), if necessary, in addition to the urethanization catalyst and solvent, the softening agent, pigment, dye, filler, nucleating agent, lubricant, mold release agent Further, an antioxidant, a light stabilizer, a flame retardant and the like may be contained.
In producing the hot melt adhesive of the present invention, it is sufficient that the constituent components of the adhesive can be heated, melted and kneaded, and ordinary hot melt production equipment can be used.
For example, a mixer, a reaction mixing tank, a single or twin screw extruder, a sigma blade mixer, a butterfly mixer, a kneader, etc., equipped with a highly compressible screw or ribbon stirrer.
The mixing temperature is preferably 60 to 250 ° C., more preferably 80 to 200 ° C., and it is preferably performed in an inert gas atmosphere such as nitrogen gas for preventing resin deterioration.

The adhesive of the present invention thus obtained is appropriately formed into a desired shape such as a block, pellet, powder, sheet or film, and can be used as a hot melt adhesive.
The method of using the hot melt adhesive of the present invention is not particularly limited. For example, when the adhesive is in the form of a block or a pellet, the adhesive is melted and then applied to a substrate to be bonded. Used by applying.
3 As an apparatus used for coating, an applicator for a normal hot melt adhesive [for example, a roll coater having a heatable melting tank (gravure roll, reverse roll, etc.), curtain coater, bead, spiral, spray, slot] And an extruder [for example, a single screw extruder, a twin screw extruder, a kneader ruder, etc.].
In the case of an apparatus such as the former, an adhesive is applied to one or both of the adherends and bonded together before cooling and solidification, or after cooling and solidification, the adherends are combined, heated again, and bonded. When bonding, it is better to pressurize, and the pressure can be released after cooling and solidification.
In the case of an apparatus like the latter, it is extruded to one or both of the adherends, and after cooling and solidification, the adherends are combined, heated again, and bonded together. When bonding, it is better to pressurize, and the pressure can be released after cooling and solidification.
Moreover, it can coextrude between adherends and can perform bonding simultaneously.

When the adhesive is powder, it is used after being applied to the adherend and then heated and bonded. The heating temperature is not particularly limited, but is preferably 10 to 20 ° C. higher than the melting point (or softening point). When bonding, it is better to pressurize, and the pressure can be released after cooling and solidification. The pressure to be applied is not particularly limited as long as sufficient adhesion can be obtained, and is preferably 10 kPa to 5 MPa. The basis weight of the powder is not particularly limited as long as a desired adhesive force can be obtained, but is preferably 10 to 500 g / m ² .

In the case where the adhesive is a sheet or film, the adhesive is sandwiched between substrates to be bonded together, heated and melted and bonded, or placed on one or both, heated and melted, and before cooling and solidification Or after cooling and solidification, the adherends are combined, heated again and bonded together. The heating temperature at the time of heating and melting is not particularly limited, but is preferably higher by 10 to 20 ° C. than the melting point (or softening point), and the heating temperature at the time of heating again is not particularly limited, but the melting point (or The temperature is preferably 10 to 20 ° C. higher than the softening point). Moreover, it is better to pressurize when bonding, and the pressure can be released after cooling and solidification. The pressure to be applied is not particularly limited as long as a desired adhesive force can be obtained, and is preferably 10 kPa to 5 MPa.
The size of the sheet or film is not particularly limited as long as it has a desired area. Although the thickness of a sheet | seat or a film does not have a restriction | limiting in particular, Preferably it is 10-500 micrometers, More preferably, it is 30-300 micrometers.

EXAMPLES Hereinafter, although an Example demonstrates this invention further, this invention is not limited to this. In the examples, “parts” represents parts by weight, and “%” represents% by weight.
(Description of abbreviations used in the following examples)
[B-1]: “Poly bd R-45HT” (manufactured by Idemitsu Petrochemical Co., Ltd .; polybutadiene glycol, hydroxyl value = 47, Mn = 2,800)
[B-2]: “Poly bd R-45M” (manufactured by Idemitsu Petrochemical Co., Ltd .; polybutadiene glycol, hydroxyl value = 42, Mn = 2,800)
[B-3]: “NISSO-PB G-1000” (manufactured by Nippon Soda Co., Ltd .; polybutadiene glycol, hydroxyl value = 86, Mn = 1,300)
[B-4]: “NISSO-PB G-3000” (manufactured by Nippon Soda Co., Ltd .; polybutadiene glycol, hydroxyl value = 37, Mn = 3,000)
[C-1]: “Pine Crystal D-6011” (manufactured by Arakawa Chemical Industries, Ltd .; rosin-containing polyol, hydroxyl value = 118.4, Mn = 950)
[C-2]: “Pine Crystal KE-359” (manufactured by Arakawa Chemical Industries, Ltd .; rosin ester, hydroxyl value = 42.8, Mn = 2,600)
[D-1]: “Sanniks FL-555” (manufactured by Sanyo Chemical Industries, Ltd .; polymer polyol, hydroxyl value = 30)
[D-2]: “Altiflow FS-7001” (manufactured by Sanyo Chemical Industries, Ltd .; polymer polyol, hydroxyl value = 28)
[D-1]: “Sanix PP-2000” (manufactured by Sanyo Chemical Industries, Ltd .; polyoxypropylene glycol, hydroxyl value = 56.9)
[E-1]: “Clearon P-85” (manufactured by Yasuhara Chemical; hydrogenated terpene resin, hydroxyl value = 0, Mn = 630)
[E-2]: “YS Resin TO-85” (manufactured by Yasuhara Chemical Co., Ltd .; aromatic modified terpene resin, hydroxyl value = 0, Mn = 750)
[F-1]: “Nicanol KL-05” (manufactured by Fudou; xylene resin, hydroxyl value = 6.3, Mn = 4,500)

[ Reference Example 1 ]
70.0 parts of [B-1] and 30.0 parts of [C-1] were charged into a separable flask equipped with a temperature controller and a stirrer and dissolved at 120 ° C., followed by vacuum dehydration (120 ° C., 133 Pa, 1 hour) )did. In a nitrogen atmosphere, 15.7 parts of MDI was added, and after aging at 80 ° C. for 4 hours, A hot melt adhesive (NCO%: 3.8%, 120 ° C melt viscosity: 5,000 mPa · s) was obtained.

[Example 1 ] to [Example 3 ]
With the combinations and parts by weight of (A) to (E) as shown in Table 1, the same operations as in [ Reference Example 1 ] were performed, respectively, to obtain the hot melt adhesives of the present invention.

[Comparative Example 1] to [Comparative Example 4]
With the combinations and parts by weight of (A) to (F) as shown in Table 1, the same operations as in [ Reference Example 1 ] were performed, respectively, to obtain comparative hot melt adhesives.

<Sample evaluation method>
1) Melt viscosity: The temperature of a sample was controlled at 120 ° C. for 15 minutes, and then measured using a B-type viscometer at the same temperature.
2) Adhesive time after coating; each of the above hot melt adhesives was melted at a temperature of 120 ° C., and was used in a 23 ° C. atmosphere using a curtain spray coating machine (hot air pressure 1.5 kg / cm ² , It is applied onto an EPDM (ethylene propylene diene) rubber sheet at a hot air temperature of 140 ° C., a gun head temperature of 130 ° C., a distance of 10 cm between the gun head and the adherend, and a coating amount of 100 g / m ^2. The time until evaluation) was measured.
3) Initial adhesive strength; applied to an EPDM rubber sheet (length 10 cm, width 10 cm, thickness 3 mm) in the same manner as 2), and after 2 minutes, a wooden thin plate (length 10 cm, width 10 cm, thickness 0. 5 mm, with a slight undulation in the shape), and bonded under a 23 ° C. atmosphere under a press pressure of 5 kgf / cm ² and a press time of 2 minutes. Thereafter, the press was released and left for 5 hours in an atmosphere of 23 ° C. and 50% RH, and the state of the adhesive was observed and evaluated according to the following criteria.
Evaluation criteria A: The area of the floating or peeling part of the wooden thin plate is 0 cm ² or more and less than 1 cm ²
○: The area of the floating and peeling parts of the wooden thin plate is 1 cm ² or more and less than 3 cm ²
X: The area of the floating and peeling part of the wooden thin plate is 3 cm ² or more.

4) Adhesive strength after curing: Bonded in the same manner as in 3), left in a constant temperature and humidity chamber at 23 ° C. and 50% RH for 1 week, and then measured at 180 ° C. peel strength. At this time, the destruction state was also observed.
The post-curing adhesive strength was measured under the condition of a tensile speed of 100 mm / min using an autograph according to JIS K6854-1999.
5) Workability of the bonded body: Bonded in the same manner as in 3), and left in a constant temperature and humidity chamber at 23 ° C. and 50% RH for 1 day. The bonded body was cut out using a saw, and the state at the time of cutting was observed and evaluated according to the following criteria.
Evaluation criteria ○: No adhesive fusion to the saw blade
×: Adhesive melted on the saw blade 6) Thermal stability; The hot melt adhesive was allowed to stand in a thermostat at 120 ° C. for 8 hours in an air atmosphere, and the viscosity change (after test / initial viscosity ratio) was measured to determine thermal stability. The closer the value is to 1, the better the thermal stability.
7) Odor, 8) Smoke; The hot melt adhesive was left in an incubator at 120 ° C. for 3 hours in an air atmosphere, and the odor and smoke generation (visually evaluated) were confirmed by five panelists.
The above results are shown in Table 2.

* 1 Cohesive failure of adhesive layer

The use of the hot melt adhesive of the present invention is not particularly limited. For example, wood, synthetic wood, wooden decorative board, various plastic molded products (molded article, film, sheet), various plastic foams (polyurethane foam, polyolefin foam), Rubber products (ethylene propylene rubber, styrene butadiene rubber, butyl rubber, etc.), metal products (copper, aluminum, stainless steel, steel plates, etc.), textile products (natural fibers, synthetic fibers, non-woven fabrics, etc.), paper, natural or synthetic leather, etc. Or it can use for adhesion | attachment of a dissimilar material.
Specifically, it can be suitably used for adhesion of construction members (floor materials, panels, boards, cloths, metals, etc.), clothing materials (fibers, woven fabrics, films, etc.), etc., but is not limited thereto. It is not something.

Claims (6)

Polyisocyanate (A), polyolefin polyol (B), Rosin having an active hydrogen which react with isocyanates (C), and Ri Na ethylenically unsaturated monomer is polymerized comprising been obtained polymer polyol (D) is obtained by reacting in a polyol, [ The equivalent ratio of (B), (C), (D) in total OH (hydroxyl group) / [(A) NCO (isocyanate group)] is 1 / 1.01 to 1/5, and [(B) + (C)] / weight ratio of (D) is 100 / (100-500) reactive hot melt adhesive Ru der. The (C) is a rosin having a hydroxyl group. The adhesive described. The adhesive according to claim 1 or 2, further comprising a tackifying resin (E). The adhesive according to any one of claims 1 to 3 , further comprising at least one selected from the group consisting of a pigment, a dye, a filler, a nucleating agent, a release agent, an antioxidant, a light stabilizer, and a flame retardant. An adherend formed by bonding with the adhesive according to any one of claims 1 to 4 . 6. The adherend according to claim 5 , wherein the adherend is a construction member.