Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
  • C08G18/40—High-molecular-weight compounds
  • C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
  • C08G18/44—Polycarbonates
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/08—Processes
  • C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/08—Processes
  • C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
  • C08G18/12—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step using two or more compounds having active hydrogen in the first polymerisation step
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
  • C08G18/40—High-molecular-weight compounds
  • C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
  • C08G18/4202—Two or more polyesters of different physical or chemical nature
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
  • C08G18/72—Polyisocyanates or polyisothiocyanates
  • C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
  • C08G18/76—Polyisocyanates or polyisothiocyanates cyclic aromatic
  • C08G18/7657—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings
  • C08G18/7664—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings containing alkylene polyphenyl groups
  • C08G18/7671—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings containing alkylene polyphenyl groups containing only one alkylene bisphenyl group
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K3/00—Use of inorganic substances as compounding ingredients
  • C08K3/34—Silicon-containing compounds
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K3/00—Use of inorganic substances as compounding ingredients
  • C08K3/34—Silicon-containing compounds
  • C08K3/346—Clay
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/16—Nitrogen-containing compounds
  • C08K5/205—Compounds containing groups, e.g. carbamates
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
  • C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
  • C09J175/04—Polyurethanes
  • C09J175/06—Polyurethanes from polyesters

Definitions

• This disclosure relates to a urethane resin-forming composition, a urethane adhesive composition, an adhesive for automotive structures, and a cured product.
• Patent Document 1 discloses such an adhesive, which comprises a first liquid containing a prepolymer obtained by reacting polyisocyanate with polyol, and a second liquid containing polyol and a catalyst, the first liquid being composed of a prepolymer and a filler obtained by reacting polyisocyanate with high molecular weight polyol (I) having a number average molecular weight of 1000 or more, and the second liquid containing high molecular weight polyol (II) having a number average molecular weight of 1000 or more and low molecular weight polyol having a number average molecular weight of less than 1000, and the molar ratio of (I), (II) and low molecular weight polyol is a predetermined amount.
• the two-liquid urethane adhesive composition of Patent Document 1 is said to have excellent storage stability of
• one aspect of the present disclosure is directed to providing a urethane resin-forming composition that contributes to the production of an adhesive having high toughness, and a composition for a urethane adhesive.
• Another aspect of the present disclosure is directed to providing an adhesive for automobile structures having high toughness, and a cured product thereof.
• a curing agent (A) containing a polyol An isocyanate-terminated prepolymer (B); Compound (C),
• the compound (C) is a compound represented by formula (1): R 1 -NHCOO-R 2 (1)
• R 1 and R 2 each independently represent an alkyl group, an alicyclic hydrocarbon group, an aryl group, or a heterocyclic group.
• the curing agent (A) is A cross-linking component (a-1), and at least one diol (a-2) selected from the group consisting of aliphatic diols and alicyclic diols.
• the isocyanate group-terminated prepolymer (B) is A polyol (b-1) having a number average molecular weight of 500 or more; Polyisocyanate (b-2),
• the curing agent (A) is A cross-linking component (a-1), and at least one diol (a-2) selected from the group consisting of aliphatic diols and alicyclic diols,
• the isocyanate group-terminated prepolymer (B) is A polyol (b-1) having a number average molecular weight of 500 or more; Polyisocyanate (b-2), and an optional cross-linking component (b-3).
• the isocyanate group-terminated prepolymer (B) is A polyol (b-1) having a number average molecular weight of 500 or more; Polyisocyanate (b-2), and an optional cross-linking component (b-3), The composition according to any one of (1) to (6), wherein the polyol (b-1) has a carbonate bond.
• the curing agent (A) is A cross-linking component (a-1), and at least one diol (a-2) selected from the group consisting of aliphatic diols and alicyclic diols,
• the isocyanate group-terminated prepolymer (B) is A polyol (b-1) having a number average molecular weight of 500 or more; Polyisocyanate (b-2), and an optional cross-linking component (b-3), The composition according to (1), wherein the polyol (b-1) has a carbonate bond.
• composition according to any one of (1) to (8), wherein the urethane group concentration of the resin obtained by curing the urethane resin-forming composition is 2000 mmol/kg or more and 5000 mmol/kg or less.
• (11) The composition according to any one of (1) to (10), wherein the compound (C) has a melting point of 100° C. or lower.
• a urethane adhesive composition comprising the urethane resin-forming composition according to any one of (1) to (11).
• An adhesive for automobile structures comprising the composition according to (12).
• a urethane resin-forming composition that contributes to the production of an adhesive having high toughness, and a composition for a urethane adhesive.
• an adhesive for automobile structures having high toughness, and a cured product it is possible to provide an adhesive for automobile structures having high toughness, and a cured product.
• a numerical range indicated using “to” indicates a range including the numerical values before and after “to” as the minimum and maximum values, respectively.
• the minimum or maximum value of a numerical range indicated using “to”, “greater than or equal to”, or “less than or equal to” can be arbitrarily combined with the maximum or minimum value of another numerical range indicated using "to”, “greater than or equal to”, or “less than or equal to”.
• the upper and lower limit values individually indicated can also be arbitrarily combined.
• the urethane resin-forming composition comprises: A curing agent (A) containing a polyol; An isocyanate-terminated prepolymer (B); Compound (C),
• the compound (C) is a compound represented by formula (1): R 1 -NHCOO-R 2 (1)
• R 1 and R 2 each independently represent an alkyl group, an alicyclic hydrocarbon group, an aryl group, or a heterocyclic group.
• a urethane resin-forming composition having high toughness can be obtained by blending the compound (C) with a urethane resin-forming composition containing a curing agent (A) containing a polyol and an isocyanate group-terminated prepolymer (B).
• the urethane resin-forming composition of one embodiment of the present disclosure contains a polyol-containing curing agent (A), an isocyanate-terminated prepolymer (B), and a compound (C), and the compound (C) is a compound represented by formula (1).
• the compound represented by formula (1) When the compound represented by formula (1) is blended into a urethane resin-forming composition containing a polyol-containing curing agent (A) and an isocyanate-terminated prepolymer (B), it exerts an effect of suppressing very localized movement of the flexible segment, so that the flexibility of the resin as a whole is not significantly impaired, and as a result of the effect of increasing rigidity, it is presumed that the toughness is improved.
• the curing agent (A) is It may contain a crosslinking component (a-1), may contain at least one diol (a-2) selected from the group consisting of aliphatic diols and alicyclic diols,
• the crosslinking component (a-1) may contain at least one diol (a-2) selected from the group consisting of aliphatic diols and alicyclic diols.
• the crosslinking component (a-1) may, for example, be a polyol having an average functionality of 3 or more.
• polyols having an average functionality of 3 or more include glycerin, trimethylolpropane, pentaerythritol, N,N-bishydroxypropyl-N-hydroxyethylamine, triethanolamine, triisopropanolamine, monomer polyols of ethylenediamine propylene oxide modified products, monomer polyols of trimethylolpropane propylene oxide modified products, and pentaerythritol propylene oxide modified products.
• polycaprolactone polyols include those obtained by ring-opening addition of cyclic esters such as ⁇ -caprolactone, ⁇ -butyrolactone, ⁇ -butyrolactone, ⁇ -valerolactone, and ⁇ -valerolactone to a polyol such as glycerin, trimethylolpropane, or pentaerythritol as an initiator.
• the cross-linking component (a-1) may contain only one of these, or two or more of them.
• examples of the aliphatic diols include aliphatic diol monomers and aliphatic diol polymers.
• examples of the alicyclic diols include alicyclic diol monomers and alicyclic diol polymers.
• Aliphatic diol monomers include, for example, ethylene glycol, 1,2-propanediol, 1,3-propanediol, 1,2-butanediol, 1,3-butanediol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, 1,8-octanediol, 1,9-nonanediol, 3-methyl-1,5-pentanediol, 3,3-dimethylolheptane, neopentyl glycol; diethylene glycol, dipropylene glycol; and the like.
• alicyclic diol monomers examples include 1,4-cyclohexanediol, cycloheptanediol, cyclooctanediol, 1,4-cyclohexanedimethanol, hydroxypropylcyclohexanol, isohexide, tricyclo[5.2.1.02,6]decane-4,8-dimethanol, and alkylene oxide adducts thereof.
• aliphatic or alicyclic diol polymer examples include aliphatic or alicyclic diol polymers containing one or more bonds selected from the group consisting of ester bonds, ether bonds, and carbonate bonds.
• Aliphatic or alicyclic polyester diols, aliphatic or alicyclic polyether diols, and aliphatic or alicyclic polycarbonate diols are more preferred, and aliphatic or alicyclic polyether diols are even more preferred.
• Aliphatic or alicyclic polycarbonate diols include, for example, ethylene glycol, 1,2-propanediol, 1,3-propanediol, 1,2-butanediol, 1,3-butanediol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, 1,8-octanediol, 1,9-nonanediol, 3-methyl-1,5-pentanediol, 3,3-dimethylolheptane, diethylene glycol, dipropylene glycol, ne Examples include those obtained by a dealcoholization or dephenolization reaction between one or more aliphatic or alicyclic diols such as dipentyl glycol, cyclohexane-1,4-diol, cyclohexane-1,4-dimethanol, and dimer acid diol, and one or more
• Aliphatic or alicyclic polyester diols include, for example, succinic acid, tartaric acid, oxalic acid, malonic acid, glutaric acid, adipic acid, pimelic acid, suberic acid, glutaconic acid, azelaic acid, sebacic acid, 1,4-cyclohexyldicarboxylic acid, ⁇ -hydromuconic acid, ⁇ -hydromuconic acid, ⁇ -butyl- ⁇ -ethylglutaric acid, ⁇ , ⁇ -diethylsuccinic acid, maleic acid, fumaric acid, and one or more other aliphatic or alicyclic dicarboxylic acids or their anhydrides; ethylene glycol, 1,2-propanediol, 1,3-propanediol, 1, Examples of the aliphatic or alicyclic polyester diol include those obtained by a condensation polymerization reaction of one or more aliphatic or alicyclic diol
• polyester-amide diols obtained by replacing a part of the aliphatic or alicyclic diol acids with aliphatic or alicyclic diamine acids such as hexamethylenediamine and isophoronediamine, or aliphatic or alicyclic amino alcohols such as monoethanolamine.
• Aliphatic or alicyclic polyether diols include, for example, ethylene glycol, 1,2-propanediol, 1,3-propanediol, 1,2-butanediol, 1,3-butanediol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, 1,8-octanediol, 1,9-nonanediol, 3-methyl-1,5-pentanediol, 3,3-dimethylolheptane, diethylene glycol, dipropylene glycol, neopentyl glycol,
• the polyether diol include polyether diols obtained by addition polymerization of alkylene oxides such as ethylene oxide, propylene oxide, butylene oxide, etc., using as an initiator an aliphatic or alicyclic compound having two active hydrogen groups, such as aliphatic or alicyclic
• examples of the polyether diol include polyether diols obtained by ring-opening polymerization of alkyl glycidyl ethers such as methyl glycidyl ether, and cyclic ether monomers such as tetrahydrofuran.
• the diol (a-2) may contain only one of these, or two or more of them.
• the number average molecular weight of diol (a-2) is preferably 4000 g/mol or less, more preferably 2500 g/mol or less, and even more preferably 1500 g/mol or less.
• the number average molecular weight in this disclosure may be any measurement method that can measure with high accuracy, for example, a method (titration method) that complies with JIS K 0070-1992.
• the isocyanate group-terminated prepolymer (B) is A polyol (b-1) having a number average molecular weight of 500 or more; Polyisocyanate (b-2), and an optional cross-linking component (b-3).
• polyols (b-1) having a number average molecular weight of 500 or more include polyols having a number average molecular weight of 500 or more and having one or more bonds selected from the group consisting of ester bonds, ether bonds, and carbonate bonds, and preferably having a carbonate bond.
• Polyester polyols, polyether polyols, and polycarbonate polyols are more preferred, polyether polyols and polycarbonate polyols are more preferred, and polycarbonate polyols are even more preferred.
• polycarbonate polyols include ethylene glycol, 1,2-propanediol, 1,3-propanediol, 1,2-butanediol, 1,3-butanediol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, 1,8-octanediol, 1,9-nonanediol, 3-methyl-1,5-pentanediol, 3,3-dimethylolheptane, diethylene glycol, dipropylene glycol, neopentyl glycol, cyclohexane-1,4-diol, cyclohexane-1,4-dimethanol, glycerin, trimethylolpropane, dimer
• polyols include those obtained by a dealcoholization or dephenolization reaction between one or more polyols such as diol acid, ethylene oxide or propyl
• the polyester polyol may be, for example, one or more of dicarboxylic acids such as phthalic acid, isophthalic acid, terephthalic acid, naphthalenedicarboxylic acid, succinic acid, tartaric acid, oxalic acid, malonic acid, glutaric acid, adipic acid, pimelic acid, suberic acid, glutaconic acid, azelaic acid, sebacic acid, 1,4-cyclohexyldicarboxylic acid, ⁇ -hydromuconic acid, ⁇ -hydromuconic acid, ⁇ -butyl- ⁇ -ethylglutaric acid, ⁇ , ⁇ -diethylsuccinic acid, maleic acid, and fumaric acid, or anhydrides thereof; ethylene glycol, 1,2-propanediol, 1,3-propanediol, 1,2-butanediol, 1,3-butanediol, 1, Examples of the polyol
• polyol (b-1) examples include polyester-amide polyols obtained by replacing a part of these alcohols with low molecular weight polyamines or low molecular weight amino alcohols such as hexamethylenediamine, isophoronediamine, and monoethanolamine.
• polyether polyols examples include ethylene glycol, 1,2-propanediol, 1,3-propanediol, 1,2-butanediol, 1,3-butanediol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, 1,8-octanediol, 1,9-nonanediol, 3-methyl-1,5-pentanediol, 3,3-dimethylolheptane, diethylene glycol, dipropylene glycol, neopentyl glycol, cyclohexane-1,4-diol, and cyclohexane-1,4-dimethanol.
• polyether polyol examples include low molecular weight polyols such as ethylene diamine, dimer acid diol, bisphenol A, bis( ⁇ -hydroxyethyl)benzene, and xylylene glycol; or low molecular weight polyamines such as ethylene diamine, propylene diamine, toluene diamine, metaphenylene diamine, diphenylmethane diamine, and xylylene diamine; and polyether polyols obtained by addition polymerization of alkylene oxides such as ethylene oxide, propylene oxide, and butylene oxide using compounds having two active hydrogen groups as initiators.
• alkylene oxides such as ethylene oxide, propylene oxide, and butylene oxide using compounds having two active hydrogen groups as initiators.
• polyether polyol examples include polyether polyols obtained by ring-opening polymerization of cyclic ether monomers such as alkyl glycidyl ethers such as methyl glycidyl ether, aryl glycidyl ethers such as phenyl glycidyl ether, and tetrahydrofuran.
• cyclic ether monomers such as alkyl glycidyl ethers such as methyl glycidyl ether, aryl glycidyl ethers such as phenyl glycidyl ether, and tetrahydrofuran.
• Polyol (b-1) may contain only one of these, or may contain two or more of them.
• the number average molecular weight of polyol (b-1) is preferably 500 or more and 10,000 or less, more preferably 500 or more and 7,000 or less, and even more preferably 500 or more and 4,000 or less.
• the polyisocyanate (b-2) may be a polyisocyanate having two or more isocyanate groups in the molecule.
• the polyisocyanate may be an organic polyisocyanate.
• the organic polyisocyanate may be an aromatic polyisocyanate, an aromatic aliphatic polyisocyanate, an aliphatic polyisocyanate, an alicyclic polyisocyanate, etc. These may be contained alone or in combination of two or more. Among these, aromatic polyisocyanates are preferred from the viewpoints of reactivity and viscosity.
• Aromatic polyisocyanates include, for example, 2,4-tolylene diisocyanate, 2,6-tolylene diisocyanate, 2,4-tolylene diisocyanate/2,6-tolylene diisocyanate mixture, 2,2'-diphenylmethane diisocyanate, 4,4'-diphenylmethane diisocyanate, 2,2'-diphenylmethane diisocyanate/4,4'-diphenylmethane diisocyanate mixture, 2,4'-diphenylmethane diisocyanate, 2,4'-diphenylmethane diisocyanate/4,4'-diphenylmethane diisocyanate mixture, 2,2'-diphenylmethane diisocyanate/2,4'- Examples include diphenylmethane diisocyanate/4,4'-diphenylmethane diisocyanate mixture, 4,4'-diphenylether diisocyanate, 2-nitrodip
• aromatic aliphatic polyisocyanates examples include 1,3-xylylene diisocyanate, 1,4-xylylene diisocyanate, 1,3-xylylene diisocyanate/1,4-xylylene diisocyanate mixtures, 1,3-bis(1-isocyanato-1-methylethyl)benzene, 1,4-bis(1-isocyanato-1-methylethyl)benzene, 1,3-bis(1-isocyanato-1-methylethyl)benzene/1,4-bis(1-isocyanato-1-methylethyl)benzene mixtures, ⁇ , ⁇ '-diisocyanato-1,4-diethylbenzene, etc.
• Aliphatic polyisocyanates include, for example, tetramethylene diisocyanate, hexamethylene diisocyanate, 2-methylpentane-1,5-diisocyanate, 3-methylpentane-1,5-diisocyanate, lysine diisocyanate, trioxyethylene diisocyanate, ethylene diisocyanate, trimethylene diisocyanate, octamethylene diisocyanate, nonamethylene diisocyanate, 2,2'-dimethylpentane diisocyanate, 2,2,4-trimethylhexane diisocyanate, decamethylene diisocyanate, butene diisocyanate, 1,3-butadiene-1,4-diisocyanate, 2,4,4-trimethylhexa
• Examples include methylene diisocyanate, 1,6,11-undecane triisocyanate, 1,3,6-hexamethylene triisocyanate, 1,8-diisocyanate
• alicyclic polyisocyanates include isophorone diisocyanate, cyclohexane diisocyanate, bis(isocyanatemethyl)cyclohexane, dicyclohexylmethane diisocyanate, methylcyclohexane diisocyanate, dicyclohexyldimethylmethane diisocyanate, 2,2'-dimethyldicyclohexylmethane diisocyanate, bis(4-isocyanate-n-butylidene)pentaerythritol, and hydrogenated dimer acid diisocyanates.
• the polyisocyanate may contain only one of these, or two or more.
• the content of polyisocyanate (b-2) in the urethane resin forming composition is preferably 750 mmol/kg or more and 3000 mmol/kg or less, and more preferably 1000 mmol/kg or more and 2500 mmol/kg or less.
• the isocyanate-terminated prepolymer (B) contains an optional crosslinking component (b-3), i.e., the isocyanate-terminated prepolymer (B) may further contain a structure derived from the crosslinking component (b-3).
• the cross-linking component (b-3) include the same as the cross-linking component (a-1).
• the total content of the crosslinkable groups in the curing agent (A) and the content of the crosslinkable groups in the isocyanate-terminated prepolymer (B) (i.e., crosslink density) in the urethane resin-forming composition is preferably 25 mmol/kg or more and 1200 mmol/kg or less, more preferably 50 mmol/kg or more and 1000 mmol/kg or less, even more preferably 100 mmol/kg or more and 800 mmol/kg or less, and particularly preferably 150 mmol/kg or more and 700 mmol/kg or less.
• the fracture toughness value (G Ic ) becomes higher, and further excellent toughness is obtained, which is preferable.
• the urethane resin-forming composition does not contain any crosslinkable groups other than the crosslinking component (a-1) and the crosslinking component (b-3)
• the total of the content of the crosslinkable groups in the curing agent (A) and the content of the crosslinkable groups in the isocyanate group-terminated prepolymer (B) is equal to the total of the content of the crosslinkable groups in the crosslinking component (a-1) and the crosslinking component (b-3).
• the crosslinkable group is a functional group that forms a crosslink. Therefore, in the case of a trifunctional polyol (e.g., glycerin), one hydroxyl group in one molecule forms a crosslink, and the remaining two hydroxyl groups do not contribute to the crosslinking, so in this case the number of crosslinkable groups is one. That is, in the case of a trifunctional polyol, the content of the crosslinkable group is synonymous with the content of the trifunctional polyol, since the trifunctional polyol has one crosslinkable group.
• a trifunctional polyol e.g., glycerin
• At least one of the polyol (b-1) and the polyisocyanate (b-2) is preferably liquid at 25° C. and 1 atmospheric pressure.
• At least one of the curing agent (A) and the isocyanate-terminated prepolymer (B) is liquid at 25°C and 1 atm.
• the curing agent (A) is A cross-linking component (a-1), and at least one diol (a-2) selected from the group consisting of aliphatic diols and alicyclic diols,
• the isocyanate group-terminated prepolymer (B) is A polyol (b-1) having a number average molecular weight of 500 or more; Polyisocyanate (b-2), and an optional cross-linking component (b-3).
• the curing agent (A) is A cross-linking component (a-1), and at least one diol (a-2) selected from the group consisting of aliphatic diols and alicyclic diols,
• the isocyanate group-terminated prepolymer (B) is A polyol (b-1) having a number average molecular weight of 500 or more; Polyisocyanate (b-2), and an optional cross-linking component (b-3),
• the polyol (b-1) has a carbonate bond. It should be noted that the urethane resin-forming composition according to this embodiment is not limited to these embodiments at all.
• Compound (C) is a compound represented by formula (1) and has one urethane bond in one molecule: R 1 -NHCOO-R 2 (1)
• R 1 and R 2 each independently represent an alkyl group, an alicyclic hydrocarbon group, an aryl group, or a heterocyclic group.
• the number of carbon atoms in the alkyl group is preferably 1 to 8, more preferably 1 to 5, and particularly preferably 1 to 3. If the number of carbon atoms in the alkyl group is within the above range, it tends to match well with the molecular chain size and provide high toughness.
• Examples of alicyclic hydrocarbon groups include cyclohexyl, cyclopentyl, and decahydronaphthyl groups.
• the alicyclic hydrocarbon groups may have a substituent, and examples of the substituent include linear or branched saturated hydrocarbon groups.
• Aryl groups include phenyl and naphthyl groups.
• the aryl groups may have a substituent, and examples of the substituent include linear or branched saturated hydrocarbon groups.
• heterocyclic groups include pyrrole rings, furan rings, thienyl groups, and phosphole rings.
• the heterocyclic groups may also have a substituent, and examples of the substituent include linear or branched saturated hydrocarbon groups.
• a combination of an alkyl group (preferably a methyl group or an ethyl group) and an alkyl group (preferably a methyl group or an ethyl group) and a combination of an alkyl group (preferably a methyl group or an ethyl group) and an aryl group (preferably a phenyl group) are preferred.
• compound (C) examples include methyl N-methylcarbamate, ethyl N-methylcarbamate, methyl N-ethylcarbamate, ethyl N-ethylcarbamate, ethyl N-phenylcarbamate, and methyl N-phenylcarbamate.
• methyl N-methylcarbamate, ethyl N-methylcarbamate, ethyl N-phenylcarbamate, and methyl N-phenylcarbamate are preferred, methyl N-methylcarbamate, ethyl N-methylcarbamate, and ethyl N-phenylcarbamate are more preferred, and methyl N-methylcarbamate is particularly preferred.
• the melting point of compound (C), measured in accordance with JIS K0064:1992, is preferably 100°C or less, more preferably 90°C or less, and even more preferably 75°C or less.
• the lower limit of the melting point of compound (C) is preferably -90°C or more. When the melting point of compound (C) is equal to or higher than the lower limit, it becomes easy to disperse compound (C) uniformly in the urethane resin, and a stable toughness improvement effect is easily obtained.
• the content of compound (C) in the urethane resin forming composition is preferably 1% by mass or more and 30% by mass or less, more preferably 2% by mass or more and 25% by mass or less, even more preferably 3% by mass or more and 20% by mass or less, and particularly preferably 4% by mass or more and 18% by mass or less.
• the content of compound (C) is equal to or more than the lower limit, the effect of improving toughness is more likely to be obtained.
• the content of compound (C) is equal to or less than the upper limit, the effect of improving toughness is more likely to be obtained without the properties of compound (C) being reflected in the urethane resin.
• the number average molecular weight of compound (C) is preferably 80 or more and 1000 or less, more preferably 100 or more and 800 or less, even more preferably 120 or more and 600 or less, and particularly preferably 140 or more and 400 or less.
• the number average molecular weight of compound (C) is equal to or more than the lower limit, the molecular chain of the urethane resin and the molecular size of compound (C) match well, and higher toughness tends to be imparted.
• compound (C) can be handled more stably in terms of viscosity and crystallinity.
• Compound (C) may be added to either or both of the curing agent (A) and the isocyanate-terminated prepolymer (B) to form a two-component adhesive, or may be used alone to form a three-component adhesive.
• the urethane group concentration of the resin obtained by curing the urethane resin-forming composition is preferably 2000 mmol/kg or more and 5500 mmol/kg or less, more preferably 2000 mmol/kg or more and 5000 mmol/kg or less, even more preferably 2600 mmol/kg or more and 4800 mmol/kg or less, and particularly preferably 2800 mmol/kg or more and 4500 mmol/kg or less.
• the urethane group concentration of the resin is equal to or more than the lower limit, the resin strength is sufficiently high and high toughness can be imparted.
• the urethane group concentration of the resin is equal to or less than the upper limit, the brittleness of the resin is suppressed, making it easier to obtain the synergistic effect of adding compound (C).
• the glass transition temperature of the resin obtained by curing the urethane resin-forming composition is preferably 60° C. or higher, more preferably 65° C. or higher, and even more preferably 70° C. or higher. In particular, in automotive applications, a glass transition temperature within this range is required from the viewpoint of strength stability in the operating temperature range.
• the glass transition temperature (Tg) was measured using a viscoelasticity measuring device.
• the measurement mode was not limited to a specific one, and a measurement mode such as a shear mode, a compression mode, a three-point bending mode, or a tension mode may be used.
• the measurement frequency was 10 Hz
• the heating rate was 2°C/min
• the measurement temperature range was -150°C to 250°C.
• the peak top temperature of the loss tangent (tan ⁇ ) was defined as Tg.
• the urethane resin-forming composition is preferably liquid (i.e., has flowability) at 25° C. and 1 atmospheric pressure.
• At least one of the curing agent (A) and the isocyanate group-terminated prepolymer (B) is preferably liquid at 25° C. and 1 atmospheric pressure.
• the urethane resin-forming composition contains a curing agent (A), an isocyanate-terminated prepolymer (B), and a compound (C). These may be a three-liquid type in which they are present separately, or a two-liquid type in which the compound (C) is mixed with at least one of the curing agent (A) and the isocyanate-terminated prepolymer (B).
• the temperature and time for mixing the curing agent (A), the isocyanate-terminated prepolymer (B), and the compound (C) may be, for example, 10 to 35°C and 1 to 60 minutes.
• the method for mixing the curing agent (A) and the isocyanate-terminated prepolymer (B) is not particularly limited, and may be, for example, a method of mixing by hand with a spatula, or a method of mixing by using a mechanical rotary mixer, a static mixer, or the like.
• a urethane adhesive composition according to one embodiment of the present disclosure includes the above-described urethane resin-forming composition.
• the urethane adhesive composition may contain other components other than the urethane resin forming composition.
• the other components are preferably those that do not react when the curing agent (A), the isocyanate group-terminated prepolymer (B) and the compound (C) are mixed.
• Examples of the other components include additives other than the components that constitute the urethane resin, such as fillers, colorants, antistatic agents, and preservatives.
• the urethane adhesive composition may contain a solvent, but the solvent content is preferably 1.0 mass % or less.
• the urethane adhesive composition may be substantially free of solvent, i.e., solvent-free. However, if a solvent is contained as an impurity, it falls into the category of being substantially "free of solvent.”
• An adhesive for automobile structure includes the above-mentioned urethane adhesive composition. This adhesive has a high fracture toughness value (G Ic ) and excellent toughness.
• a cured product according to one embodiment of the present disclosure is a cured product of the above-mentioned urethane resin-forming composition.
• Examples 1 to 15 In a 2L stirring vessel filled with nitrogen, the raw materials of the curing agent were charged and stirred according to the recipes shown in Tables 1 to 14, and the mixture was stirred for about 1 to 3 hours while maintaining the temperature in the stirring vessel at 70 to 80°C, to obtain various curing agents (A).
• R (resin) represents the ratio of NCO groups to OH groups (NCO/OH), which is a value that can be adjusted by the amount of the main agent and the amount of the curing agent.
• the right-hand example marked with "-” shows an example in which no filler was added
• the left-hand example shows an example in which a filler was added. Therefore, the fracture toughness value (G Ic ) and the cohesive failure rate were measured in the example in which a filler was added, and Tg was measured in the example in which a filler was not added.
• the raw materials for the main agent (isocyanate-terminated prepolymer) (B) were added to a 2 L stirring vessel filled with nitrogen according to the recipes shown in Tables 1 to 14 and stirred. The temperature inside the stirring vessel was then kept at 70 to 80°C, and the urethane reaction was allowed to proceed for about 2 to 5 hours to obtain various isocyanate-terminated prepolymers (B).
• DCB test fracture toughness value
• Resin thickness Adjusted with a spacer to 0.35 mm.
• Teflon registered trademark
• Test piece shape Contoured type was used.
• Test substrate S50C steel (electroless nickel plating treatment) was used.
• Test conditions Pulled at 2 mm/min, and the fracture toughness value GIc was calculated based on the maximum load.
• the compound (C) which had been preliminarily heated to 70°C was added to the base material (isocyanate group-terminated prepolymer (B)) so that the amount of the compound (C) in the resin composition was 2.5 to 10 mass %, and the mixture was mixed and degassed.
• a filler talc 50% by mass/zeolite 50% by mass
• the curing agent (A) was further added and mixed with stirring for 30 seconds, and then the mixture was applied to a substrate and fixed with a clamp, followed by curing in two stages at 25° C. for 30 minutes and 180° C. for 30 minutes.
• a viscoelasticity measuring device (DMA7100; Hitachi High-Tech Science Corporation) was used, and Tg was obtained from the peak top temperature of the loss tangent (tan ⁇ ) when the measurement mode was tension, the measurement frequency was 10 Hz, the heating rate was 2°C/min, and the measurement temperature range was -150°C to 250°C.

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