JP7288820B2 - Two-component hardening spray material - Google Patents

Description

TECHNICAL FIELD The present invention relates to a two-component hardening spray material, and more particularly to a two-component hardening spray material that is used as a flooring material for building materials, a waterproof material, an industrial lining material, a thick-film protective material, and an antirust material.

BACKGROUND ART Conventionally, two-component hardening sprayed materials are known as materials such as floor materials for building materials, waterproof materials, industrial lining materials, thick-film protective materials, and anticorrosion materials.

In such a two-component curing spray material, the main agent and the curing agent are separately prepared, and when used, the main agent and the curing agent are sprayed at a predetermined flow rate ratio using a known spray device, and the application is performed. Spray on the surface.

Examples of such a two-component curing spray material include a reaction product of a polyol and a polyisocyanate containing a polyisocyanate in which an NCO group is directly bonded to an aromatic ring and a polyisocyanate in which an NCO group is directly bonded to an aromatic ring. A two component curing spray material comprising an A component comprising a prepolymer and a B component comprising a polyol, specifically 4,4'-diphenylmethane diisocyanate (MDI) and 3-isocyanatomethyl-3,5, A two-component curing spray material has been proposed that includes an A component containing a prepolymer obtained from 5-trimethylcyclohexyl isocyanate (IPDI) and a B component containing a polyoxypropylene polyol (for example, Examples of Patent Document 1 1).

JP-A-6-49409

From the viewpoint of workability, the two-component curing spray material is required to further shorten the gel time in the reaction between the main agent and the curing agent.

An object of the present invention is to provide a two-component hardening spray material with a short gel time.

The present invention [1] comprises a main agent and a curing agent, the main agent contains a xylylene diisocyanate monomer, and the xylylene diisocyanate monomer is 5% by mass or more of the main agent. wherein the curing agent comprises a polyamine, a polyol and a catalyst, the catalyst comprises a metallate of a carboxylic acid or a metallate of a carboxylic acid and a free carboxylic acid, and the catalyst However, when the carboxylic acid metallate and the free carboxylic acid are included, the carboxylic acid metallate is larger than the free carboxylic acid on a mass basis, and is a two-component curing spray material be.

In the present invention [2], the metal acid salt of the carboxylic acid is selected from the group consisting of lead carboxylate, bismuth carboxylate, and tin carboxylate, and the content of the metal acid salt of the carboxylic acid is contains the two-component curing spray material according to the above [1], which is 90% by mass or more with respect to the catalyst.

The present invention [3] includes the two-component curable spray material according to the above [1] or [2], wherein the main agent includes an isocyanate group-terminated prepolymer that is a reaction product of polyisocyanate and macropolyol. I'm in.

The two-component curing spray material of the present invention comprises a main agent and a curing agent.

In addition, the main agent contains a predetermined proportion of xylylene diisocyanate monomer.

Thereby, odor can be reduced and gel time can be shortened.

In addition, the physical properties (tensile strength, tear strength, elongation at break and heat resistance) of the cured film obtained by using this two-component curing spray material can be improved.

In addition, the curing agent contains a carboxylic acid metal salt, or contains a carboxylic acid metal salt and a free carboxylic acid in a predetermined compounding ratio.

Thereby, the gel time can be shortened.

1. Two-Component Curing Spray Material The two-component curing spray material of the present invention comprises a main agent and a curing agent.

Specifically, the two-component curing spray material is a coating kit for spray coating, and includes a main agent and a curing agent separately.
2. Main Agent The main agent contains a predetermined proportion of xylylene diisocyanate monomer.

Examples of xylylene diisocyanate include 1,2-xylylene diisocyanate, 1,3-xylylene diisocyanate and 1,4-xylylene diisocyanate, preferably 1,3-xylylene diisocyanate.

These xylylene diisocyanate monomers can be used alone or in combination of two or more.

The content of the xylylene diisocyanate monomer is 5% by mass or more, preferably 10% by mass or more, more preferably 15% by mass or more, and still more preferably 20% by mass or more, relative to the main agent, Also, for example, it is 90% by mass or less, preferably 60% by mass or less, more preferably 50% by mass or less, particularly preferably 40% by mass or less, and most preferably 30% by mass or less.

When the content of the xylylene diisocyanate monomer is at least the above lower limit, the odor can be reduced and the gel time can be shortened.

In addition, physical properties (tensile strength, tear strength, elongation at break and heat resistance) of a cured film (described later) obtained by using this two-component curing spray material can be improved.

As a method for preparing such a main agent, the amount of xylylene diisocyanate monomer is adjusted so that the number of isocyanate groups of the monomer of xylylene diisocyanate is greater than the number of hydroxyl groups of the macropolyol (described later) on a molar basis. A method of preparing a first isocyanate group-terminated prepolymer (first method) by reacting a polymer with a macropolyol (described later), other isocyanates (isocyanate components excluding xylylene diisocyanate monomers, described later. ) and a macropolyol (described later) to prepare a second isocyanate group-terminated prepolymer, and then mix the second isocyanate group-terminated prepolymer with a monomer of xylylene diisocyanate ( second method).

Each method described above will be described in detail below.
2.1. First method In the first method, the xylylene diisocyanate monomer is added so that the number of isocyanate groups in the xylylene diisocyanate monomer is greater than the number of hydroxyl groups in the macropolyol (described later) on a molar basis, A main agent (first main agent) is prepared by reacting it with a macropolyol (described later) to prepare a first isocyanate group-terminated prepolymer.

Although details will be described later, in the first method, the first isocyanate group terminal pretreatment is performed so that the number of isocyanate groups in the xylylene diisocyanate monomer is greater than the number of hydroxyl groups in the macropolyol (described later) on a molar basis. By preparing the polymer, unreacted xylylene diisocyanate monomer is left. Thus, a first main agent containing a predetermined proportion of xylylene diisocyanate monomer is prepared.

The first isocyanate group-terminated prepolymer is a polyurethane prepolymer having two or more free isocyanate groups at its molecular end.

To prepare the first isocyanate group-terminated prepolymer, a first polyisocyanate containing a monomer of xylylene diisocyanate is reacted with a macropolyol.

The first polyisocyanate contains only xylylene diisocyanate monomers.

The macropolyol has two or more hydroxyl groups, preferably two, and a number average molecular weight of, for example, 250 or more, preferably 400 or more, preferably 500 or more, and for example, 3000 or less, preferably 2500. Oligomers of 2000 or less, more preferably 2000 or less, include, for example, polyether polyols, polyester polyols, polycarbonate polyols, polyurethane polyols, epoxy polyols, vegetable oil polyols, polyolefin polyols, acrylic polyols, and vinyl monomer-modified polyols. .

Macropolyols preferably include polyether polyols, polyester polyols and polycarbonate polyols.

Examples of polyether polyols (specifically, polyether diols and polyether triols) include polyoxyalkylene polyols such as polyoxypropylene polyols and polytetramethylene ether polyols.

Polyoxypropylene polyols include, for example, low-molecular-weight polyols (preferably dihydric alcohols) or aromatic/aliphatic polyamine-initiated addition polymers of propylene oxide (random propylene oxide and ethylene oxide and/or including block copolymers.).

Examples of polytetramethylene ether polyols include ring-opening polymer (polytetramethylene ether glycol (PTMEG)) obtained by cationic polymerization of tetrahydrofuran, alkyl-substituted tetrahydrofuran in polymerization units such as tetrahydrofuran, and the above dihydric alcohol. Examples thereof include copolymerized amorphous polytetramethylene ether glycol.

Examples of polyester polyols include polycondensates obtained by reacting low-molecular-weight polyols and polybasic acids under known conditions.

Examples of polybasic acids include oxalic acid, malonic acid, succinic acid, methylsuccinic acid, glutaric acid, adipic acid, 1,1-dimethyl-1,3-dicarboxypropane, and 3-methyl-3-ethylglutaric acid. , azelaic acid, sebacic acid, other saturated aliphatic dicarboxylic acids (C11-13) such as maleic acid, fumaric acid, itaconic acid, other unsaturated aliphatic dicarboxylic acids such as orthophthalic acid, isophthalic acid, terephthalic acid , toluenedicarboxylic acid, naphthalenedicarboxylic acid, other aromatic dicarboxylic acids such as hexahydrophthalic acid, other alicyclic dicarboxylic acids such as dimer acid, hydrogenated dimer acid, other carboxylic acids such as het acid, and acid anhydrides derived from these carboxylic acids, such as oxalic anhydride, succinic anhydride, maleic anhydride, phthalic anhydride, 2-alkyl (C12-C18) succinic anhydride, tetrahydrophthalic anhydride, tri Melitic acid, and acid halides derived from these carboxylic acids, such as oxalic acid dichloride, adipic acid dichloride, sebacic acid dichloride and the like.

In addition, as the polyester polyol, for example, a plant-derived polyester polyol, specifically, a low molecular weight polyol as an initiator, a hydroxyl group-containing vegetable oil fatty acid (for example, castor oil fatty acid containing ricinoleic acid, 12-hydroxystearic acid Hydroxycarboxylic acids such as hydrogenated castor oil fatty acids, etc.) are condensed under known conditions to obtain vegetable oil-based polyester polyols.

As polyester polyols, for example, ring-opening polymerization of lactones such as ε-caprolactone and γ-valerolactone and lactides such as L-lactide and D-lactide using a low-molecular-weight polyol as an initiator. Polycaprolactone polyol, polyvalerolactone polyol, and lactone-based polyester polyols such as those obtained by copolymerizing these with the dihydric alcohols described above.

Polycarbonate polyols include, for example, a ring-opening polymer of ethylene carbonate using a low-molecular-weight polyol as an initiator, and 1,4-butanediol, 1,5-pentanediol, and 3-methyl-1,5-pentanediol. and amorphous polycarbonate polyols obtained by copolymerizing a dihydric alcohol such as 1,6-hexanediol and a ring-opening polymer.

These macropolyols can be used alone or in combination of two or more.

More preferably, the macropolyols include polyether polyols, more preferably polyoxypropylene polyols.

Then, to prepare the first isocyanate group-terminated prepolymer, the first polyisocyanate and the macropolyol are reacted.

Specifically, the first polyisocyanate (monomer of xylylene diisocyanate) and the macropolyol are separated into isocyanate groups in the first polyisocyanate (monomer of xylylene diisocyanate) against active hydrogen groups (hydroxyl groups) in the macropolyol. equivalent ratio (NCO/active hydrogen group) is excessive, for example, 2.01 or more, preferably 3.5 or more, more preferably 5.0 or more, and, for example, 30 or less, preferably is formulated (mixed) so as to be 20 or less, and in a reaction vessel, for example, room temperature (25 ° C.) or higher, preferably 50 ° C. or higher, and, for example, 150 ° C. or lower, preferably 120 ° C. or lower Then, for example, the reaction (urethanization reaction) is allowed to proceed for 0.5 hours or more, preferably 2 hours or more, and for example, 18 hours or less, preferably 10 hours or less.

In the above reaction, if the above equivalent ratio is 2.01 or more, the isocyanate groups of the xylylene diisocyanate monomer can be excessive on a molar basis with respect to the hydroxyl groups of the macropolyol. As a result, the unreacted xylylene diisocyanate monomer can remain in a predetermined proportion.

In addition, in the urethanization reaction, if necessary, an organic solvent can be added to prepare the first isocyanate group-terminated prepolymer in the presence thereof.

Examples of organic solvents include ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone and cyclohexanone; nitriles such as acetonitrile; alkyl esters such as methyl acetate, ethyl acetate, butyl acetate and isobutyl acetate; Aliphatic hydrocarbons such as hexane, n-heptane and octane, alicyclic hydrocarbons such as cyclohexane and methylcyclohexane, aromatic hydrocarbons such as toluene, xylene and ethylbenzene, and methyl cellosolve acetate. , ethyl cellosolve acetate, methyl carbitol acetate, ethyl carbitol acetate, ethylene glycol ethyl ether acetate, propylene glycol methyl ether acetate, 3-methyl-3-methoxybutyl acetate, ethyl-3-ethoxypropionate and other glycol ether esters ethers such as diethyl ether, tetrahydrofuran, dioxane; halogenated aliphatic hydrocarbons such as methyl chloride, methylene chloride, chloroform, carbon tetrachloride, methyl bromide, methylene iodide, dichloroethane; and polar aprotons such as N-methylpyrrolidone, dimethylformamide, N,N'-dimethylacetamide, dimethylsulfoxide, hexamethylphosphonylamide, and the like.

These organic solvents can be used alone or in combination of two or more.

The mixing ratio of the organic solvent is appropriately set according to the purpose and application.

In addition, in the above urethanization reaction, a urethanization catalyst such as amines or organometallic compounds can be added as necessary.

Examples of amines include tertiary amines such as triethylamine, triethylenediamine, bis-(2-dimethylaminoethyl)ether and N-methylmorpholine; quaternary ammonium salts such as tetraethylhydroxyammonium; imidazole; and imidazoles such as 2-ethyl-4-methylimidazole.

Examples of organometallic compounds include tin acetate, tin octoate, tin oleate, tin laurate, dibutyltin diacetate, dimethyltin dilaurate, dibutyltin dilaurate, dibutyltin dimercaptide, dibutyltin maleate, dibutyltin dilaurate, and dibutyltin. Organotin compounds such as dineodecanoate, dioctyltin dimercaptide, dioctyltin dilaurate, dibutyltin dichloride; organolead compounds such as lead octanoate and lead naphthenate; organonickel compounds such as nickel naphthenate; , organic cobalt compounds such as cobalt naphthenate, organic copper compounds such as copper octenoate, and organic bismuth compounds such as bismuth octylate and bismuth neodecanoate.

Furthermore, examples of urethanization catalysts include potassium salts such as potassium carbonate, potassium acetate, and potassium octylate.

These urethanization catalysts can be used alone or in combination of two or more.

Thereby, the first polyisocyanate and the macropolyol react to obtain a first isocyanate group-terminated prepolymer.

The isocyanate group content (NCO group content, NCO %) of such a first isocyanate group-terminated prepolymer is, for example, 10% by mass or more and, for example, 15% by mass or less.

The first isocyanate group-terminated prepolymer can also be prepared as a solution of the solvent described above, in which case the solid content concentration is, for example, 10% by mass or more, preferably 20% by mass or more. Also, for example, it is 90% by mass or less, preferably 80% by mass or less.

Further, as described above, in the reaction between the first polyisocyanate and the macropolyol, the isocyanate groups of the monomer of xylylene diisocyanate are in excess of the hydroxyl groups of the macropolyol on a molar basis. Unreacted xylylene diisocyanate monomer remains.

Therefore, the first main agent contains the first isocyanate group-terminated prepolymer, which is the reaction product of the first polyisocyanate and the macropolyol, and the unreacted xylylene diisocyanate monomer.

The content of the xylylene diisocyanate monomer is 5% by mass or more, preferably 10% by mass or more, more preferably 15% by mass or more, and still more preferably 20% by mass or more, relative to the first main agent. Also, for example, it is 90% by mass or less, preferably 60% by mass or less, more preferably 50% by mass or less, particularly preferably 40% by mass or less, and most preferably 30% by mass or less.

If the content of the xylylene diisocyanate monomer in the first main component is at least the above lower limit, the odor can be reduced and the gel time can be shortened.

In addition, physical properties (tensile strength, tear strength, elongation at break and heat resistance) of a cured film (described later) obtained by using this two-component curing spray material can be improved.

The content ratio of the above-mentioned xylylene diisocyanate monomer can be obtained by, for example, HPLC measurement.

Further, if necessary, a predetermined amount of unreacted xylylene diisocyanate monomer can be removed from the first main agent by known removal means such as distillation or extraction.

Moreover, a plasticizer can be blended into the first main agent, if necessary.

Examples of plasticizers include dioctyl adipate (DOA), diisononyl adipate (DINA), diisodecyl adipate (DIDA), and di-n-alkyl adipate, preferably diisodecyl adipate (DIDA). mentioned.

The mixing ratio of the plasticizer is, for example, 1% by mass or more, and is, for example, 10% by mass or less, preferably 5% by mass or less, relative to the first main agent.

In the first main agent, the content of isocyanate groups (NCO group content, NCO %) is, for example, 5% by mass or more, preferably 10% by mass or more, and is, for example, 20% by mass or less.

The viscosity (25° C.) of the first main agent is, for example, 1500 mPa·s or less, preferably 1000 mPa·s or less, more preferably 700 mPa·s or less, still more preferably 500 mPa·s or less. It is 100 mPa·s or more.

If the above viscosity is equal to or less than the above upper limit, the first main agent can be easily sprayed.

The viscosity of the first main agent can be determined using a spindle-type rotational viscometer TV-25 L model manufactured by Toki Sangyo Co., Ltd., or the like.
2.2. Second method In the second method, a second isocyanate group-terminated prepolymer is prepared by reacting another isocyanate with a macropolyol, and then the second isocyanate group-terminated prepolymer and a xylylene diisocyanate monomer. A main agent (second main agent) is prepared by mixing with the body.

Although details will be described later, in the second method, a second isocyanate group-terminated prepolymer is blended with a predetermined proportion of a xylylene diisocyanate monomer to obtain a second isocyanate containing a predetermined proportion of the xylylene diisocyanate monomer. Prepare the main ingredient.

The second isocyanate group-terminated prepolymer is a polyurethane prepolymer having two or more free isocyanate groups at its molecular end.

To prepare the second isocyanate group-terminated prepolymer, a second polyisocyanate containing another isocyanate is reacted with the macropolyol.

The second polyisocyanate contains only other isocyanates. In other words, the second polyisocyanate does not contain xylylene diisocyanate monomers.

Examples of other isocyanates include polyisocyanate monomers such as aromatic polyisocyanates, araliphatic polyisocyanates (excluding xylylene diisocyanate), alicyclic polyisocyanates, and aliphatic polyisocyanates.

Aromatic polyisocyanates include, for example, 4,4'-, 2,4'- or 2,2'-diphenylmethane diisocyanate or mixtures thereof (MDI), 2,4- or 2,6-tolylene diisocyanate or mixtures thereof aromatic diisocyanates such as (TDI), o-tolidine diisocyanate, 1,5-naphthalene diisocyanate (NDI), m- or p-phenylene diisocyanate or mixtures thereof, 4,4'-diphenyl diisocyanate, 4,4'-diphenyl ether diisocyanate is mentioned.

Examples of araliphatic polyisocyanates include araliphatic diisocyanates such as 1,3- or 1,4-tetramethylxylylene diisocyanate or mixtures thereof (TMXDI), ω,ω'-diisocyanate-1,4-diethylbenzene. mentioned.

Alicyclic polyisocyanates include, for example, 3-isocyanatomethyl-3,5,5-trimethylcyclohexyl isocyanate (isophorone diisocyanate, IPDI), 4,4′-, 2,4′- or 2,2′-methylenebis (cyclohexyl isocyanate) or mixtures thereof (H ₁₂ MDI), 1,3- or 1,4-bis(isocyanatomethyl)cyclohexane or mixtures thereof (H ₆ XDI), bis(isocyanatomethyl)norbornane (NBDI), 1 ,3-cyclopentene diisocyanate, 1,4-cyclohexane diisocyanate, 1,3-cyclohexane diisocyanate, methyl-2,4-cyclohexane diisocyanate and methyl-2,6-cyclohexane diisocyanate.

Aliphatic polyisocyanates include, for example, hexamethylene diisocyanate (hexane diisocyanate) (HDI), pentamethylene diisocyanate (pentane diisocyanate) (PDI), tetramethylene diisocyanate, trimethylene diisocyanate, 1,2-, 2,3- or 1 ,3-butylene diisocyanate, 2,4,4- or 2,2,4-trimethylhexamethylene diisocyanate.

Further, other polyisocyanates include polyisocyanate derivatives, for example, multimers of other polyisocyanates described above (e.g., dimers, trimers (e.g., isocyanurate-modified, iminooxadiazinedione-modified) , pentamers, heptamers, etc.), allophanate modified products (e.g., other polyisocyanates described above and allophanate modified products produced by reaction with monohydric alcohols or dihydric alcohols), polyol modified products (e.g., Polyol modified product (alcohol adduct) produced by reaction of other polyisocyanate and trihydric alcohol (e.g., trimethylolpropane, etc.), biuret modified product (e.g., other polyisocyanate described above, water or biuret-modified products produced by reaction with amines), urea-modified products (e.g., urea-modified products produced by reaction of other polyisocyanates and diamines described above), oxadiazinetrione-modified products (e.g., Oxadiazinetrione produced by the reaction of other polyisocyanates with carbon dioxide, etc.), modified carbodiimides (modified carbodiimides produced by the decarboxylation condensation reaction of other polyisocyanates described above, etc.), modified uretdione, Also included are uretonimine modified products.

Other polyisocyanates preferably include polyisocyanate monomers, more preferably aromatic polyisocyanate monomers, and more preferably tolylene diisocyanate monomers.

Examples of the macropolyol include those similar to the macropolyols listed for the first main component, preferably polyether polyols, and more preferably polyoxypropylene polyols from the viewpoint of shortening the gel time.

Then, in order to prepare the second isocyanate group-terminated prepolymer, the second polyisocyanate and the macropolyol are added to the equivalent ratio of the isocyanate groups in the second polyisocyanate to the active hydrogen groups in the macropolyol (NCO/active hydrogen group ) is, for example, less than 2, preferably 1.8 or less, or, for example, 1.6 or more, and is mixed in a reaction vessel, for example, at room temperature (25 ° C.) or more, preferably is 50° C. or higher, for example, 150° C. or lower, preferably 120° C. or lower, for example, 0.5 hours or longer, preferably 2 hours or longer, and, for example, 18 hours or shorter, preferably 10 hours. The following reaction (urethanization reaction) is carried out.

In addition, in the urethanization reaction, if necessary, the above-described organic solvent can be added to prepare the second isocyanate group-terminated prepolymer in its presence.

Moreover, in the above-mentioned urethanization reaction, for example, the above-described urethanization catalyst can be added as necessary.

Thereby, the second polyisocyanate and the macropolyol react to obtain a second isocyanate group-terminated prepolymer.

The isocyanate group content (NCO group content, NCO%) of such a second isocyanate group-terminated prepolymer is, for example, 2.0% by mass or more, preferably 3.0% by mass or more, and , for example, 10% by mass or less, preferably 5% by mass or less.

The second isocyanate group-terminated prepolymer can also be prepared as a solution of the solvent described above, in which case the solid content concentration is, for example, 10% by mass or more, preferably 20% by mass or more. Also, for example, it is 90% by mass or less, preferably 80% by mass or less.

Next, in the second method, a second main agent is prepared by mixing a second isocyanate group-terminated prepolymer and a xylylene diisocyanate monomer.

The mixing ratio of the second isocyanate group-terminated prepolymer is, for example, 60 parts by mass or more with respect to the total amount of 100 parts by mass of the second isocyanate group-terminated prepolymer and the xylylene diisocyanate monomer. , 80 parts by mass or less, and the mixing ratio of the xylylene diisocyanate monomer is, for example, 20 parts by mass or more and, for example, 40 parts by mass or less.

The content of the xylylene diisocyanate monomer is 5% by mass or more, preferably 10% by mass or more, more preferably 15% by mass or more, and still more preferably 20% by mass, relative to the second main agent. For example, it is 90% by mass or less, preferably 60% by mass or less, more preferably 50% by mass or less, particularly preferably 40% by mass or less, and most preferably 30% by mass or less.

In the second main agent, when the content of the xylylene diisocyanate monomer is at least the above lower limit, the odor can be reduced and the gel time can be shortened.

In addition, physical properties (tensile strength, tear strength, elongation at break and heat resistance) of a cured film (described later) obtained by using this two-component curing spray material can be improved.

As a result, the second main agent containing the second isocyanate group-terminated prepolymer, which is the reaction product of the second polyisocyanate and the macropolyol, and the xylylene diisocyanate monomer is obtained.

In addition, the above-described plasticizer can be blended with the second main agent, if necessary.

The plasticizer preferably includes diisodecyl adipate (DIDA).

The mixing ratio of the plasticizer is, for example, 1% by mass or more, and is, for example, 10% by mass or less, preferably 5% by mass or less, relative to the second main agent.

In addition, as described above, in the second method, the second isocyanate group-terminated prepolymer is prepared by reacting the second polyisocyanate and the macropolyol, so the unreacted second polyisocyanate (second polyisocyanate monomer) may remain.

In such a case, the second main agent comprises a second isocyanate group-terminated prepolymer that is a reaction product of the second polyisocyanate and the macropolyol, a xylylene diisocyanate monomer, and an unreacted second polyisocyanate. and isocyanate.

The content of the unreacted second polyisocyanate is, for example, less than 1% by mass, preferably 0.8% by mass or less, relative to the second main agent.

Further, as described above, in the reaction between the second polyisocyanate and the macropolyol, the equivalent ratio (NCO/active hydrogen group) of the isocyanate groups in the second polyisocyanate to the active hydrogen groups in the macropolyol is less than 2. Then, the amount of unreacted second polyisocyanate can be reduced.

Specifically, the content of the unreacted second polyisocyanate can be, for example, less than 1% by mass, preferably 0.8% by mass or less, relative to the second main agent.

If the content of the unreacted second polyisocyanate is equal to or less than the above upper limit, the odor can be reduced and the gel time can be shortened.

The content ratio of the unreacted second polyisocyanate can be determined, for example, by HPLC measurement.

Further, if necessary, a predetermined amount of unreacted second polyisocyanate can be removed from the second main agent by known removal means such as distillation or extraction.

In the second main agent, the isocyanate group content (NCO group content, NCO %) is, for example, 5% by mass or more, preferably 10% by mass or more, and is, for example, 20% by mass or less.

The viscosity (25° C.) of the second main agent is, for example, 1500 mPa·s or less, preferably 1200 mPa·s or less, and is, for example, 100 mPa·s or more.

If the above viscosity is equal to or less than the above upper limit, the second main agent can be easily sprayed.

The viscosity of the second main agent can be determined using a spindle-type rotational viscometer TV-25 L model manufactured by Toki Sangyo Co., Ltd., or the like.

As described above, the first main component contains the first isocyanate group-terminated prepolymer that is the reaction product of the first polyisocyanate and the macropolyol.

Also, the second main agent contains a second isocyanate group-terminated prepolymer that is a reaction product of the second polyisocyanate and the macropolyol.

That is, both the first main agent and the second main agent are polyisocyanate (the first polyisocyanate in the first main agent or the second polyisocyanate in the second main agent) and the isocyanate group-terminated polyisocyanate that is the reaction product of the macropolyol. A prepolymer (a first isocyanate group-terminated prepolymer in the first main agent or a second isocyanate group-terminated prepolymer in the second main agent) is included.

If the main agent contains an isocyanate group-terminated prepolymer, which is a reaction product of polyisocyanate and macropolyol, the viscosity of the main agent can be easily adjusted, and the elongation at break of the resulting cured film (described later) can be made appropriate. can do. In addition, in the spray coating described later, the volume ratio of the main agent and the curing agent must be constant (for example, 1:1), and prepolymerization enables an appropriate formulation.

In the first method described above, the first polyisocyanate contains only xylylene diisocyanate monomers, but the first polyisocyanate can also contain other polyisocyanates as described above.

Other polyisocyanates include aromatic polyisocyanate monomers, more preferably tolylene diisocyanate monomers, from the viewpoint of shortening the gel time.

In such a case, in the reaction between the first polyisocyanate (monomer of xylylene diisocyanate and other polyisocyanate) and the macropolyol, a predetermined proportion of unreacted monomer of xylylene diisocyanate to make it remain.

In such a case, in the first polyisocyanate, the blending ratio of the xylylene diisocyanate monomer and the blending ratio of the other polyisocyanate are appropriately selected.

Also, in such a case, the first main component is a first isocyanate group-terminated prepolymer which is a reaction product of a first polyisocyanate (a monomer of xylylene diisocyanate and other polyisocyanate) and a macropolyol. , a monomer of xylylene diisocyanate, or a first isocyanate group-terminated prepolymer that is a reaction product of a first polyisocyanate (monomer of xylylene diisocyanate and other polyisocyanate) and a macropolyol , xylylene diisocyanate monomers, and other polyisocyanate monomers.
3. Curing Agents Curing agents include polyamines, polyols, and catalysts.
3.1. Polyamine Polyamine has an amino group as an active hydrogen group, for example, aromatic polyamine, araliphatic polyamine, alicyclic polyamine, aliphatic polyamine, amino alcohol, polyoxyethylene group-containing polyamine, primary amino group , or amino group-containing compounds such as alkoxysilyl compounds having primary and secondary amino groups, hydrazine or derivatives thereof.

Examples of aromatic polyamines include 4,4'-diphenylmethanediamine, tolylenediamine, diethyltoluenediamine and the like, preferably diethyltoluenediamine.

Araliphatic polyamines include, for example, 1,3- or 1,4-xylylenediamine or mixtures thereof.

Examples of alicyclic polyamines include 3-aminomethyl-3,5,5-trimethylcyclohexylamine (also known as isophoronediamine), 4,4′-dicyclohexylmethanediamine, 2,5(2,6)-bis( aminomethyl)bicyclo[2.2.1]heptane, 1,4-cyclohexanediamine, 1-amino-3-aminomethyl-3,5,5-trimethylcyclohexane, bis-(4-aminocyclohexyl)methane, diaminocyclohexane , 3,9-bis(3-aminopropyl)-2,4,8,10-tetraoxaspiro[5,5]undecane, 1,3- and 1,4-bis(aminomethyl)cyclohexane and mixtures thereof etc.

Examples of aliphatic polyamines include ethylenediamine, propylenediamine, 1,3-propanediamine, 1,4-butanediamine, 1,5-pentanediamine, 1,6-hexamethylenediamine, diethylenetriamine, triethylenetetramine, and tetraethylene. pentamine, 1,2-diaminoethane, 1,2-diaminopropane, 1,3-diaminopentane and the like.

Amino alcohols include, for example, 2-((2-aminoethyl)amino)ethanol (alias: N-(2-aminoethyl)ethanolamine), 2-((2-aminoethyl)amino)-1-methylpropanol (alias: N-(2-aminoethyl)isopropanolamine) and the like.

Polyoxyethylene group-containing polyamines include, for example, polyoxyalkylene ether diamines such as polyoxyethylene ether diamine. More specifically, for example, PEG #1000 diamine manufactured by NOF, Jeffamine ED-2003, EDR-148, XTJ-512, D-2000 manufactured by Huntsman, and the like can be mentioned.

Examples of alkoxysilyl compounds having a primary amino group or a primary amino group and a secondary amino group include γ-aminopropyltrimethoxysilane, γ-aminopropyltriethoxysilane, N-phenyl-γ Alkoxysilyl compounds having a primary amino group such as aminopropyltrimethoxysilane, N-β (aminoethyl) γ-aminopropyltrimethoxysilane (also known as N-2-(aminoethyl)-3-aminopropyltrimethoxysilane) methoxysilane), N-β (aminoethyl) γ-aminopropyltriethoxysilane (alias: N-2-(aminoethyl)-3-aminopropyltriethoxysilane), N-β (aminoethyl) γ-aminopropyl Methyldimethoxysilane (alias: N-2-(aminoethyl)-3-aminopropylmethyldimethoxysilane), N-β (aminoethyl) γ-aminopropylmethyldiethoxysilane (alias: N-2-(aminoethyl) -3-aminopropylmethyldiethoxysilane) and alkoxysilyl compounds having a primary amino group and a secondary amino group.

Examples of hydrazine or derivatives thereof include hydrazine (including hydrates), succinic dihydrazide, and adipic dihydrazide.

Polyamines preferably include aromatic polyamines, more preferably diethyltoluenediamine.

Polyamines can be used singly or in combination of two or more.
3.2. Polyol Polyol has a hydroxyl group as an active hydrogen group, and includes, for example, the above-described macropolyols, preferably polyether polyols, and more preferably polyether diols and polyether triols.

Polyols can be used singly or in combination of two or more. Preferably, polyetherdiol and polyethertriol are used in combination.

When polyether diol and polyether triol are used together, the mixing ratio of polyether diol is, for example, 60 parts by mass or more with respect to the total amount of 100 parts by mass of polyether diol and polyether triol. , 80 parts by mass or less, and the mixing ratio of the polyether triol is, for example, 20 parts by mass or more and, for example, 40 parts by mass or less.
3.3. Catalyst The catalyst comprises a metallate of a carboxylic acid or comprises a metallate of a carboxylic acid and a free carboxylic acid, preferably consisting of a metallate of a carboxylic acid or a metalate of a carboxylic acid Consists of salts and free carboxylic acids.

A metal salt of a carboxylic acid is a catalyst (urethanization catalyst) that promotes the urethanization reaction, and includes, for example, lead carboxylate, bismuth carboxylate, tin carboxylate, nickel naphthenate, and the like. Carboxylic acid nickel salts, for example, carboxylic acid cobalt salts such as cobalt naphthenate, carboxylic acid copper salts such as, for example, copper octoate, and the like can be mentioned.

Carboxylate lead salts include, for example, lead octylate, lead neodecanoate, lead stearate, lead oleate and the like, preferably lead octylate, lead neodecanoate, and more preferably lead octylate. .

The bismuth carboxylate includes, for example, bismuth octoate, bismuth neodecanoate, bismuth stearate, bismuth oleate and the like, preferably bismuth octylate, bismuth neodecanoate, more preferably bismuth octylate. .

Examples of tin carboxylates include tin octoate, tin neodecanoate, tin stearate, tin oleate, and tin laurate.

From the viewpoint of further shortening the gel time, the metal acid salt of carboxylic acid is preferably selected from the group consisting of lead carboxylate, bismuth carboxylate and tin carboxylate. acid lead salts and bismuth carboxylates.

The metal acid salts of carboxylic acids may be used singly or in combination of two or more.

The free carboxylic acid is a catalyst (urea formation catalyst) that promotes the urea formation reaction, and examples thereof include free octylic acid, free naphthenic acid, free octenoic acid, free octylic acid, free neodecanoic acid, and the like. and preferably free octylic acid.

When the catalyst contains a carboxylic acid metal salt and a free carboxylic acid, the carboxylic acid metal salt is blended in a larger amount than the free carboxylic acid on a mass basis.

The gel time can be shortened if the metal salt of carboxylic acid is larger than the free carboxylic acid on a mass basis.

Specifically, on a mass basis, the content of the carboxylic acid metal salt is, for example, more than 50% by mass, preferably 70% by mass or more, more preferably 90% by mass or more, relative to the catalyst. There is, and it is 99 mass % or less, for example. In addition, based on mass, the content of free carboxylic acid is, for example, 1% by mass or more relative to the catalyst, and is, for example, less than 50% by mass, preferably 30% by mass or less, more preferably It is 10% by mass or less.

If the content of the metal acid salt of carboxylic acid is at least the above lower limit, the gel time can be further shortened.

As noted above, the catalyst comprises a carboxylic acid metallate, or a carboxylic acid metallate and a free carboxylic acid, but preferably, from the standpoint of availability, the catalyst comprises a carboxylic acid More preferably, the catalyst consists of the metallate of the carboxylic acid and the free carboxylic acid.

In the case where the catalyst contains a carboxylic acid metal salt and a free carboxylic acid, the catalyst is prepared by blending the free carboxylic acid with the carboxylic acid metal salt in the predetermined ratio described above. be able to.

The content of the metal salt of carboxylic acid and the content of free carboxylic acid in the catalyst on a mass basis can be obtained from the amount charged in the preparation described above.
3.3. Preparation of Curing Agent To prepare the curing agent, a polyamine, a polyol, and a catalyst are mixed.

The blending ratio of polyamine is, for example, 10 parts by mass or more, preferably 20 parts by mass or more, and for example, 40 parts by mass or less with respect to 100 parts by mass of the total amount of polyamine and polyol. The mixing ratio is, for example, 60 parts by mass or more, preferably 80 parts by mass or more, and is, for example, 90 parts by mass or less.

The blending ratio of the catalyst is, for example, 0.5 parts by mass or more, preferably 3 parts by mass or more, and for example, 10 parts by mass or less, preferably 5 parts by mass, with respect to 100 parts by mass of the total amount of polyamine and polyol. Part by mass or less.

This gives a curing agent.

The viscosity (25° C.) of the curing agent is, for example, 1000 mPa·s or less, preferably 700 mPa·s or less, more preferably 500 mPa·s or less, and for example, 100 mPa·s or more.

If the above viscosity is equal to or less than the above upper limit, the curing agent can be easily sprayed.

The viscosity of the curing agent can be determined using a spindle-type rotational viscometer TV-25 L model manufactured by Toki Sangyo Co., Ltd., or the like.
4. How to use the two-component hardening spray material The two-component hardening spray material is used in the first step of preparing the two-component hardening spray material, and then spraying the two-component hardening spray material onto the work surface. and a second step.

In the first step, a two-component hardening spray material is prepared.

Specifically, each of the main agent and the curing agent is prepared by the method described above.

In a second step, a two-component hardening spray material is spray applied to the work surface.

Specifically, first, each of the main agent and the curing agent is fed to a known spray device.

As a known spray device, for example, a high-pressure collision mixing type spray device in which the main agent and the curing agent are sprayed at high pressure and mixed in the air, for example, the main agent and the curing agent are premixed in the device. Examples include a static mixer type spray device.

Specific examples of the high-pressure impingement mixing type spray device include Reactor (manufactured by Graco).

Specific examples of the static mixer type spray device include Jet Spray (manufactured by Kawata Co., Ltd.).

Then, using a known spray device, the main agent and the curing agent are sprayed so that the equivalent ratio (isocyanate group/active hydrogen group) of the isocyanate group in the main agent to the active hydrogen group (hydroxyl group, amino group) in the curing agent is, for example, , 0.6 or more, preferably 1.0 or more, and, for example, 2 or less.

The ejection pressure (liquid pressure) is, for example, 0.8 N/mm ² or more and, for example, 1.5 N/mm ² or less.

The ejected main agent and curing agent are mixed in the air and applied to the construction surface. After that, on the construction surface, for example, 5 seconds or more, preferably 10 seconds or more, and, for example, 20 seconds or less, preferably 15 seconds or less, more preferably 12 seconds or less (gel time). (urethane urea film) is formed.

If the gel time is at least the above lower limit, it is possible to prevent the two-component hardening spray material from sticking to a known spray device. Moreover, delamination can be suppressed when the spray coating is repeated several times.

If the gel time is equal to or less than the above upper limit, it is possible to suppress the occurrence of dripping when the two-component curing spray material is spray-coated on the upright surface.

That is, if the gel time is within the above range, the two-component hardening spray material can be continuously spray-coated on flat and upright surfaces.

In addition, when a static mixer type spray device is used as the spray device, the main agent and the curing agent are mixed in advance in the device. Sometimes.

On the other hand, in this two-component curing spray material, the gel time can be within the above range (preferably 10 seconds or more and 15 seconds or less). You can buy time until

The thickness of the cured film is, for example, 0.5 mm or more and, for example, 4 mm or less.

From the viewpoint of lowering the viscosity of the main agent and the curing agent, the main agent and the curing agent can be heated to, for example, 40° C. or higher and 70° C. or lower, if necessary, during the spray coating.

Specifically, when a high-pressure impingement mixing type spray device is used as the spray device, the main agent and the curing agent are heated to, for example, 50° C. or higher and 70° C. or lower, and a static mixer type spray device is used as the spray device. When used, the main agent and curing agent are heated to, for example, 25° C. or higher and 40° C. or lower.

Further, if necessary, the above spray coating can be repeated several times to adjust the thickness of the cured film to a predetermined thickness.

When spray coating is repeated, the two-component curing spray material is spray coated so that the thickness of the cured film is, for example, 0.3 mm or more and 0.6 mm or less in one spray coating.

Shore A hardness of the resulting cured film (according to JIS K7312 (1996)) is, for example, 80 A or more, preferably 87 A or more, more preferably 89 A or more, and for example, 95 A or less, preferably 91A or less.

In this two-component curing spray material, since the main agent contains a predetermined proportion of xylylene diisocyanate monomer, the physical properties (tensile strength, tear strength, elongation at break and heat resistance) can be improved.

Specifically, the tensile strength (according to JIS K7312 (1996)) of the cured film is, for example, 10 MPa or more, preferably 12 MPa or more, and is, for example, 30 MPa or less.

Further, the tear strength of the cured film (according to JIS K7312 (1996)) is, for example, 46 N/mm or more, preferably 52 N/mm or more, more preferably 55 N/mm or more. mm or less.

Further, the elongation at break of the cured film (according to JIS K7312 (1996)) is, for example, 300% or more, preferably 370% or more, more preferably 450% or more, and, for example, 480% or less. be.

Then, according to this two-component curing spray material, since a cured film having excellent physical properties can be formed, for example, floor materials for building materials, waterproof materials, industrial lining materials, thick film protective materials and It can be suitably used as an antirust material.
5. Effects This two-component hardening spray material comprises a main agent and a hardening agent.

The main agents (the first main agent and the second main agent) contain a predetermined proportion of xylylene diisocyanate monomer.

Thereby, odor can be reduced and gel time can be shortened.

In addition, the physical properties (tensile strength, tear strength, elongation at break and heat resistance) of the cured film obtained by using this two-component curing spray material can be improved.

In addition, the curing agent contains a carboxylic acid metal salt, or contains a carboxylic acid metal salt and a free carboxylic acid in a predetermined compounding ratio.

Thereby, the gel time can be shortened.

Specific numerical values such as the mixing ratio (content ratio), physical property values, and parameters used in the following description are described in the above "Mode for Carrying Out the Invention", the corresponding mixing ratio (content ratio ), physical properties, parameters, etc. can. In the description below, "parts" and "%" are based on mass unless otherwise specified.
1. Details of Components Each component used in each example and each comparative example is described below.
PPG D-2000: polyoxypropylene glycol, number average molecular weight 2000, Mitsui Chemicals PPG D-700: polyoxypropylene glycol, number average molecular weight 700, Mitsui Chemicals PPG D-400: polyoxypropylene glycol, number average molecular weight 400 , Mitsui Chemicals Cosmonate T-80: 2,4-isomer/2,6-isomer ratio 80/20 tolylene diisocyanate, Mitsui Chemicals DETDA: diethyltoluenediamine, Ethacure #100, Albemarle ED- 56: Polyether diol, molecular weight 2000, Mitsui Chemicals EP-550N: Polyether triol, molecular weight 3000, Mitsui Chemicals Neostan U-600H: Bismuth octylate/octylic acid mixture with a bismuth octylate content of 93%, Nitto Kako Co., Ltd. Neostan U-600: Bismuth octylate/octylic acid mixture with a bismuth octylate content of 58%, manufactured by Nitto Kako Co., Ltd. Lead Neodecanoate 30%: Lead octylate/mineral spirit mixture with a lead octylate content of 80%, manufactured by Nippon Kagaku Sangyo Co., Ltd. 2. Preparation of Two-Component Curing Spray 2.1. Measurement of unreacted xylylene diisocyanate monomer concentration or unreacted tolylene diisocyanate monomer concentration Unreacted xylylene diisocyanate monomer concentration or unreacted tolylene diisocyanate was determined by HPLC measurement.

The measurement conditions for HPLC measurement are shown below.
Measurement conditions Apparatus: Shimadzu Corporation high performance liquid chromatography LC-20 type Column: Shimadzu Corporation Shim-Pack CLC-SIL (6 mm ID × 15 cm)
Column temperature: 25°C
Mobile phase: n-hexane/dichloroethane/methanol Retention time of XDI: 6.1 minutes Quantification method: calibration curve method 2.2. Preparation of main agent Preparation example 1 (main agent 1)
616.9 g of PPG D-2000, 22.9 g of PPG D-700, and 360.1 g of xylylene diisocyanate were charged into a 1 L separable flask and heated at 90° C. so that the equivalent ratio (NCO/OH) was 5.6. It was reacted for 4 hours.

As a result, an isocyanate group-terminated prepolymer (XDI prepolymer) was obtained.

In the above reaction, the unreacted xylylene diisocyanate monomer was 24% by mass.

Thus, a main component 1 containing an isocyanate group-terminated prepolymer (XDI prepolymer) and a xylylene diisocyanate monomer (24% by mass) was prepared.

Further, in the main agent 1, the isocyanate group content was 13.2% by mass, the viscosity (25° C.) was 420 mPa·s, and the liquid specific gravity was 1.07.

Preparation Example 2 (main ingredient 2)
849.7 g of PPG D-2000, 8.6 g of PPG D-400, and 141.8 g of Cosmonate T-80 were charged and reacted at 90° C. for 3 hours so that the equivalent ratio (NCO/OH) was 1.8. rice field.

As a result, the isocyanate group-terminated prepolymer (TDI prepolymer, isocyanate group content 3.0% by mass, viscosity (25 ° C.) 22000 mPa s, unreacted tolylene diisocyanate monomer content 0.7 mass %) was obtained.

Next, 245.8 g of a xylylene diisocyanate monomer and 25.0 g of DINA (diisononyl adipate) as a plasticizer were added to 729.2 g of the above TDI prepolymer.

Thus, a main agent 2 containing an isocyanate group-terminated prepolymer (TDI prepolymer) and a xylylene diisocyanate monomer (24.5% by mass) was prepared.

Further, in the main agent 2, the isocyanate group content was 13.2% by mass, the viscosity (25° C.) was 1000 mPa·s, and the liquid specific gravity was 1.05.

Preparation Example 3 (main agent 3)
295.3 g of 3-isocyanatomethyl-3,5,5-trimethylcyclohexyl isocyanate (IPDI) and 25.0 g of DINA (diisononyl adipate) as a plasticizer were added to 679.7 g of the above TDI prepolymer.

Thus, a main component 3 containing an isocyanate group-terminated prepolymer (TDI prepolymer) and an IPDI monomer (29.5% by mass) was prepared.

Further, in the main agent 3, the isocyanate group content was 13.2% by mass, the viscosity (25° C.) was 900 mPa·s, and the liquid specific gravity was 1.03.

Preparation Example 4 (main agent 4)
559.7 g of PPG D-2000, 20.8 g of PPG D-700, 419.5 g of IPDI, 200 ppm of stannus octoate was added as a reaction catalyst, and the equivalent ratio (NCO/OH) was 80 so that it was 6.1. °C for 5 hours.

As a result, an isocyanate group-terminated prepolymer (IPDI prepolymer) was obtained.

In the above reaction, the unreacted IPDI monomer was 28.2% by mass.

Thus, a main agent 4 containing an isocyanate group-terminated prepolymer (IPDI prepolymer) and an IPDI monomer (28.2% by mass) was prepared.

Further, in the main agent 4, the isocyanate group content was 13.2% by mass, the viscosity (25° C.) was 550 mPa·s, and the liquid specific gravity was 1.03.

Preparation Example 5 (main agent 5)
PPG D-2000 587.1 g, PPG D-700 21.8 g, bis(isocyanatomethyl) norbornane (NBDI) 391.1 g, as a reaction catalyst, stannas octoate was added so as to be 200 ppm, and the equivalent ratio (NCO /OH) was 5.9 at 80° C. for 5 hours.

As a result, an isocyanate group-terminated prepolymer (NBDI prepolymer) was obtained.

In the above reaction, the unreacted NBDI monomer was 25.7% by mass.

Thus, a main agent 5 containing an isocyanate group-terminated prepolymer (NBDI prepolymer) and an NBDI monomer (25.7% by mass) was prepared.

Further, in the main agent 5, the isocyanate group content was 15.3% by mass, the viscosity (25° C.) was 430 mPa·s, and the liquid specific gravity was 1.07.
2.3. Preparation of Curing Agent Preparation Example 6 (Curing Agent 1)
20.1 g of DETDA, 59.9 g of ED-56, 20.0 g of EP-550N, and 4.0 g of Neostan U-600H as a catalyst were blended.

Thus, curing agent 1 (liquid density 1.00, viscosity (25° C.) 550 mPa·s) was prepared.

Preparation Examples 7 to 10 (curing agent 2 to curing agent 5)
Curing Agents 2 to 5 were prepared in the same manner as in Preparation Example 6, except that the formulation was changed according to Table 1.

The liquid densities of curing agents 2 to 5 are all 1.00, the viscosity of curing agent 2 (25° C.) is 520 mPa·s, and the viscosity of curing agent 3 (25° C.) is 530 mPa. · s, the viscosity (25°C) of curing agent 4 was 600 mPa·s, and the viscosity (25°C) of curing agent 5 was 580 mPa·s.
2.4. Preparation of Two-Component Curing Spray Materials Examples 1 to 5, Comparative Examples 1 to 4
As described above, the main agent and the curing agent were separately prepared, and the main agent and the curing agent were combined according to Table 1 to prepare a two-component curing spray material comprising the main agent and the curing agent.
3. Evaluation (spray molding (spray conditions))
Spray molding was performed using the two component cured spray material of each example and each comparative example.

Specifically, each of the main agent and the curing agent was fed to a two-liquid high-pressure spray machine (manufactured by Graco) equipped with a probler gun in the reactor. In addition, the mixing chamber is No. 1 was used. Then, the temperatures of the main agent and the curing agent were adjusted to about 60° C., and the liquid pressure was adjusted to 10.3 N/mm ² , respectively, and sprayed onto a room-temperature polypropylene plate (thickness: about 2 mm).

The compounding ratio (mass ratio and volume ratio) and equivalent ratio (isocyanate group/amino group) of the main agent and the curing agent were changed according to Table 1.
(Odor)
Based on the spray conditions described above, the odor when the two-component curing spray material was sprayed was evaluated.

Specifically, the atmosphere during spraying in the spray booth was sensory evaluated.

Odor was evaluated according to the following criteria.
O: The odor did not bother me.
x: The odor bothered me.

Table 1 shows the results.
(gel time)
After spraying the two-component hardening spray material of each example and each comparative example based on the spray conditions described above, the gel time was measured by touching with a finger.

Table 1 shows the results.
(Hardness (Shore A))
After spraying the two-component hardening spray material of each example and each comparative example based on the spray conditions described above, the material was cured at room temperature for one week to obtain a hardened film.

After that, the hardness (Shore A) of the cured film was measured using a Shore A type durometer GS-719N manufactured by Teclock.
(tensile strength, tear strength and elongation at break)
After spraying the two-component hardening spray material of each example and each comparative example based on the spray conditions described above, the material was cured at room temperature for one week to obtain a hardened film.

Thereafter, the tensile strength, tear strength and elongation at break of the cured film were measured using a universal tensile tester Autograph AGS-X manufactured by Shimadzu Corporation at a crosshead speed of 500 mm/min.

Table 1 shows the results.
(Heat-resistant)
After spraying the two-component hardening spray material of each example and each comparative example based on the spray conditions described above, the material was cured at room temperature for one week to obtain a hardened film.

After that, the cured film was cut into a size of 5 cm×5 cm and used as a sample. Next, this sample was placed in a thermostatic chamber of type SPH-202 (manufactured by Espec Co., Ltd.) capable of temperature control at 120±° C., and left at 120° C. for 1 week.

Heat resistance was evaluated according to the following criteria.
O: The sample did not melt.
Δ: The surface of the sample melted.
x: The sample melted.

Claims (2)

Equipped with a main agent and a curing agent,
The main component contains an isocyanate group-terminated prepolymer which is a reaction product of polyisocyanate and macropolyol, and a monomer of xylylene diisocyanate,
The monomer of the xylylene diisocyanate is 5% by mass or more with respect to the main agent,
the curing agent comprises a polyamine, a polyol, and a catalyst;
the catalyst comprises a metallate of a carboxylic acid, or comprises a metallate of a carboxylic acid and a free carboxylic acid;
When the catalyst contains the metal salt of the carboxylic acid and the free carboxylic acid, the metal salt of the carboxylic acid is larger than the free carboxylic acid on a mass basis, Two-component hardening spray. The metal acid salt of the carboxylic acid is selected from the group consisting of lead carboxylate, bismuth carboxylate, and tin carboxylate,
2. The two-component hardening spray material according to claim 1, wherein the content of said metal acid salt of carboxylic acid is 90% by mass or more with respect to said catalyst.