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WO2022049797A1 - Composition de solvant et son application - Google Patents

Composition de solvant et son application Download PDF

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Publication number
WO2022049797A1
WO2022049797A1 PCT/JP2021/003350 JP2021003350W WO2022049797A1 WO 2022049797 A1 WO2022049797 A1 WO 2022049797A1 JP 2021003350 W JP2021003350 W JP 2021003350W WO 2022049797 A1 WO2022049797 A1 WO 2022049797A1
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WIPO (PCT)
Prior art keywords
resin
cleaning
component
solvent composition
weight
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PCT/JP2021/003350
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English (en)
Japanese (ja)
Inventor
和音 小柳津
昌平 河野
慎平 長田
旻又 金子
清 嶋田
Original Assignee
株式会社カネコ化学
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
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Application filed by 株式会社カネコ化学 filed Critical 株式会社カネコ化学
Priority to CN202180002715.9A priority Critical patent/CN113710788A/zh
Priority to CN202410715053.5A priority patent/CN118772962A/zh
Publication of WO2022049797A1 publication Critical patent/WO2022049797A1/fr

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    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D7/00Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/22Organic compounds
    • C11D7/28Organic compounds containing halogen
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D7/00Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/50Solvents

Definitions

  • the present invention relates to a solvent composition and its use. Specifically, the present invention uses a solvent composition, a cleaning agent, a cleaning aerosol composition, a solubilizer for a cured resin, an adhesive for a cured resin, and a resin coating using the solvent composition. Regarding the agent.
  • organic solvents containing halogenated hydrocarbon solvents such as heptane and 1,1,1-trichlorethylene are used as base solvents for solvent compositions used in cleaning agents and the like.
  • Most of the organic solvents containing heptane described in Patent Document 1 are designated as volatile organic compounds (VOCs).
  • Volatile organic compounds are a general term for organic chemical substances that easily volatilize in the atmosphere at normal temperature and pressure. Volatile organic compounds (VOCs), when released into the environment, produce suspended particulate matter and photochemical oxidants, which can cause air pollution such as photochemical smog. In addition, 90% or more of photochemical oxidants are composed of ozone, and are called “tropospheric ozone” to distinguish them from “stratospheric ozone”.
  • p-chlorobenzotrifluoride is a solvent that is not classified as VOC in the US EPA and the Chinese regulation GB38508-2020, and the solvent composition based on this solvent has an environmental load. It was found that the properties are low and the solubility of resins and the like is excellent.
  • the present invention has the following configurations. [1] (A) A solvent composition containing p-chlorobenzotrifluoride. [2] Further, (b1) nitro compound, (b2) ether, (b3) ester (excluding (b2) ether), (b4) alcohol (excluding (b2) ether), (b5) amide compound, (b6).
  • the solvent composition of [1] which comprises one or more selected from the group consisting of fluoroethers.
  • it contains one or more selected from the group consisting of (b8) hydrobromocarbon and (b6-1) hydrochloroolefin, (b8) is 1-bromopropane, and (b6) is trans-.
  • the solvent composition of [1] which is 1,2-dichloroethylene.
  • [5] Further selected from the group consisting of (b8) hydrobromocarbon, (b1) nitro compound, (b2-2) cyclic ether (excluding (b2-3) epoxide) and (b2-3) epoxide.
  • the solvent composition of [1], which comprises one or more of the above, and (b8) is 1-bromopropane.
  • solvent composition [8] Further, it contains one or more selected from the group consisting of (b5) amide compounds, and (b5) is N-methyl-2-pyrrolidone, 3-methoxy-N, N-dimethylpropanamide.
  • Solvent composition [9] The solvent composition of [1], further comprising a combination of sulfuric acid and one or more selected from the group consisting of (b13) alkylbenzene sulfonic acid and salts thereof. [10] The solvent composition of [9], further comprising one or more selected from the group consisting of (b9) hydrofluorocarbons and (b10) hydrofluoroethers.
  • the cleaning agent of [12] the step (1A): the step of immersing the object to be cleaned in the cleaning agent of [12]
  • the step (1B) the cleaning agent of [12] to the component (A).
  • a cleaning agent for use in a method for cleaning an object to be cleaned which comprises a step of generating steam containing the above and bringing the object to be cleaned into contact with the generated steam containing the component (A).
  • the resin is one or more selected from acrylic resin, polycarbonate resin, acrylonitrile / butadiene / styrene resin, silicone resin, polyamide resin, urethane resin, polyacetal resin, epoxy resin, styrol resin and polyvinyl chloride resin. , [17] solubilizer. [19] An adhesive for a cured resin using the solvent composition according to any one of [1] to [11]. [20] The resin is one or more selected from acrylic resin, polycarbonate resin, acrylonitrile / butadiene / styrene resin, silicone resin, polyamide resin, urethane resin, polyacetal resin, epoxy resin, styrol resin and polyvinyl chloride resin.
  • the resin is one or more selected from acrylic resin, polycarbonate resin, acrylonitrile / butadiene / styrene resin, silicone resin, polyamide resin, urethane resin, polyacetal resin, epoxy resin, styrol resin and polyvinyl chloride resin.
  • coating agent [21] coating agent.
  • the present invention also includes the following aspects. [1a] For cleaning the object to be cleaned to which one or more selected from the group consisting of oily stains, oil, flux and uncured resin of the solvent composition according to any one of [1] to [11] is attached.
  • a cleaning agent a solvent for a cured resin, or an adhesive for a cured resin.
  • [4a] A method for producing a resin coating agent, which comprises a step of dissolving a cured resin in the solvent composition according to any one of [1] to [11].
  • [5a] Use of an aerosol composition containing the solvent composition according to any one of [1] to [11] and an injection gas as an aerosol composition for cleaning.
  • [6a] A method for producing an aerosol composition for cleaning, which uses an aerosol composition containing the solvent composition according to any one of [1] to [11] and an injection gas.
  • a solvent composition having a low environmental load and an excellent solubility of a resin or the like is provided.
  • FIG. 1 is a diagram illustrating an outline of the cleaning system 1.
  • FIG. 2 is a diagram showing an outline of the cleaning system 2.
  • FIG. 3 is a diagram illustrating an outline of the cleaning system 3.
  • FIG. 4 is a diagram showing an outline of the cleaning system 4.
  • the solvent composition comprises (A) p-chlorobenzotrifluoride.
  • the solvent composition has excellent solubility of resins and the like.
  • resin, etc. means at least oil, flux, uncured resin, or a cured product of resin.
  • the solvent composition has a low environmental load.
  • the organic solvent cleaning agent in the Chinese regulation GB38508-2020 is not restricted by GB38508-2020 as long as the VOC content is 900 g / L or less in the composition.
  • the content of p-chlorobenzotrifluoride, which is not applicable to VOC can be deducted when calculating the VOC content. Therefore, by combining p-chlorobenzotrifluoride with various organic solvents, GB38508-2020 It is possible to provide a cleaning agent that is not applicable to the above.
  • the component (A) is the main ingredient of the solvent composition.
  • p-chlorobenzotrifluoride (CAS No. 98-56-6) is PCBTF (parachlorobenzotrifluoride), p-chlorobenzotrifluoride, 4-chlorobenzotrifluoride, 4-chlorobenzotrifluoride, p- It is also called chlorotrifluorotoluene, p-chloro- ⁇ , ⁇ , ⁇ -trifluorotoluene, 1-chloro-4- (trifluoromethyl) benzene and the like.
  • the solvent composition contains (A) structural isomers such as 2-chlorotrifluoromethylbenzene and 3,4-dichlorotrifluoromethylbenzene that can be produced in the process of producing p-chlorobenzotrifluoride, and dichlorosubstituted products. You may.
  • the solvent composition may contain (B) a further component and (C) an additive other than the component (A) as long as the effect of the present invention is not impaired. Further, the solvent composition may contain impurities of the component (A), the component (B) and the component (C) as components other than the component (A), the component (B) and the component (C).
  • Further ingredients include (b1) nitro compounds, (b2) ethers, (b3) esters (excluding (b2) ethers), (b4) alcohols (excluding (b2) ethers), and (b5) amides.
  • the nitro compound is not particularly limited as long as it is a compound having one or more nitro groups in the molecule.
  • Examples of the component (b1) include nitroalkanes such as nitromethane, nitroethane, 1-nitropropane and 2-nitropropane.
  • the component (b1) may be nitromethane.
  • the ether is an ether solvent containing a carbon atom, a hydrogen atom and an ether bond (—O—), which may be linear or branched, and may be cyclic or acyclic.
  • the component (b2) include (b2-1) acyclic ether, (b2-2) cyclic ether (excluding (b2-3) epoxide), (b2-3) epoxide and the like.
  • acyclic ether examples include dipropyl ether, diisopropyl ether, diethyl ether, diisobutyl ether, dibutyl ether, methyl tertiary butyl ether, methyl cellosolve, ethyl cellosolve, isopropyl cellosolve, diethylene glycol monomethyl ether, triethylene glycol monomethyl ether, and diethylene glycol.
  • Monoethyl ether triethylene glycol monoethyl ether, ethylene glycol monopropyl ether, diethylene glycol monopropyl ether, triethylene glycol monopropyl ether, ethylene glycol monobutyl ether, diethylene glycol monobutyl ether, triethylene glycol monobutyl ether, propylene glycol monomethyl ether, di Diethyl glycol monomethyl ether, tripropylene glycol monomethyl ether, propylene glycol monoethyl ether, dipropylene glycol monoethyl ether, tripropylene glycol monoethyl ether, propylene glycol monopropyl ether, dipropylene glycol monopropyl ether, tripropylene glycol monopropyl ether.
  • Glycolmethyl ether ethylene glycol ethyl ether, 3-methoxy-3-methyl-1-butanol, diethylene glycol monohexyl ether, diethylene glycol ethylmethyl ether , Dipropylene glycol ethylmethyl ether and the like.
  • Specific examples of the cyclic ether include tetrahydrofuran, methyltetrahydrofuran, 4-methyltetrahydropyran, 1,4-dioxane, 1,3-dioxolane and the like.
  • epoxides include 1,2-butylene oxide, epichlorohydrin, epibromohydrin, propylene oxide, cyclohexene oxide, cyclopentene oxide, pentene oxide, normal hexene oxide, heptene oxide, octene oxide, and methylglycidyl ether.
  • Ethyl glycidyl ether isopropyl glycidyl ether, other alkyl glycidyl ethers, alkyl glycidyl esters and the like.
  • the component (b2) may be propylene glycol monomethyl ether.
  • Examples of the (b3) ester (excluding the (b2) ether) include a monoester solvent, an ester solvent having two carbonyl groups, a carbonic acid ester solvent, and a cyclic ester solvent.
  • Specific examples of the component (b3) include methyl acetate, ethyl acetate, normal propyl acetate, isopropyl acetate, butyl acetate, sec-butyl acetate, methoxybutyl acetate, amyl acetate, soybean fatty acid methyl ester, methyl lactate, and ethyl lactate.
  • the component (b3) may be one or more selected from the group consisting of dimethyl carbonate and ⁇ -butyrolactone.
  • Examples of the (b4) alcohol (excluding the (b2) ether) include monoalcohol-based solvents.
  • Specific examples of the component (b4) include ethanol, methanol, 1-propanol, isopropyl alcohol, 1-butanol, isobutyl alcohol, tertiary butanol, secondary butyl alcohol, benzyl alcohol, diacetone alcohol, and 2-propin-1.
  • -Alcohol, 2-ethylhexanol and the like can be mentioned.
  • the amide compound is a cyclic or acyclic compound having an amide bond.
  • the component (b5) N-methyl-2-pyrrolidone, N-ethyl-2-pyrrolidone, 2-pyrrolidone, 3-methoxy-N, N-dimethylpropanamide, 3-butoxy-N, N-dimethylpropanamide , Dimethylformamide, dimethylacetamide, dimethylacetamide, 1,3-dimethyl-2-imidazolidinone and the like.
  • the component (b5) may be one or more selected from the group consisting of N-methyl-2-pyrrolidone and 3-methoxy-N, N-dimethylpropanamide.
  • Chloroolefin ⁇ (B6) Chloroolefin ⁇ (B6)
  • the chloroolefin is an olefin compound containing a carbon atom and a chlorine atom and may contain a hydrogen atom.
  • Examples of the component (b6) include (b6-1) hydrochloroolefin, (b6-2) perchloroolefin and (b6-3) chlorofluoroolefin.
  • Examples of the component (b6-1) include trans-1,2-dichloroethylene and trichlorethylene.
  • Examples of the component (b6-2) include tetrachlorethylene (perchloroethylene) and the like.
  • the components (b6-3) include 1,1-dichloro-2,3,3,3-tetrafluoropropene (CFO-1214ya) and 1,1,2-trichloro-3,3,3-trifluoropropene (1,1,2-trichloro-3,3,3-trifluoropropene). CFO-1213xa) and the like.
  • hydrofluoroolefin ⁇ (B7) Hydrofluoroolefin ⁇ (B7)
  • the hydrofluoroolefin is a halogenated fluoroolefin compound which may contain one or more atoms selected from the group consisting of a chlorine atom and a bromine atom.
  • the components (b7) include cis-1-chloro-3,3,3-trifluoropropene (HCFO-1233zd (Z)) and (E) -1-chloro-2,3,3-trifluoropropene (((b7)).
  • the hydrofluoroolefin is (E) -1-chloro-2,3,3-trifluoropropene ((E) -1-chloro-2,3,3-trifluoro-1-propene, HCFO-1233yd (E)). ), (Z) -1-chloro-2,3,3-trifluoropropene ((Z) -1-chloro-2,3,3-trifluoro-1-propene, HCFO-1233yd (Z)) or cis. It may be -1-chloro-3,3,3-trifluoropropene (HCFO-1233zd (Z)).
  • CELEFIN registered trademark
  • 1233Z HCFO-1233zd (Z)
  • AMOLEA registered trademark
  • AS-300 manufactured by AGC Co., Ltd.
  • Z -1-chloro-2,3,3-trifluoropropene (HCFO-1233yd (Z)) and stabilizers Mixture of))
  • Hydrobromocarbon is a compound consisting only of a carbon atom, a bromine atom and a hydrogen atom.
  • Examples of the component (b8) include normal propyl bromide (1-bromopropane), isobutyl bromide and the like.
  • Hydrofluorocarbon ⁇ (B9) Hydrofluorocarbon (HFC) is a compound consisting only of a carbon atom, a fluorine atom and a hydrogen atom, and is a compound having no carbon-carbon double bond.
  • the component (b9) include 1,1,1,3,3-pentafluorobutane (HFC-365mfc) and 1,1,2,2,3,3,4-heptafluorocyclopentane (HFC-c447ef). ), 1,1,1,2,2,3,4,4,5,6,6-tridecafluorooctane, 1,1,1,2,2,3,4,5,5 , 5-Decafluoropentane (HFC-43-10mee).
  • 1,1,1,3,3-pentafluorobutane is a commercially available product such as Solcan (registered trademark) 365 mfc (manufactured by Nippon Solvay Co., Ltd.), 1, 1, 2, 2 , 3,3,4-Heptafluorocyclopentane includes Zeorora (registered trademark) H (manufactured by Zeon Corporation, Japan).
  • Hydrofluoroether ⁇ (B10) Hydrofluoroolefins are compounds containing a carbon atom, a fluorine atom, a hydrogen atom and an ether bond (—O—).
  • component (b10) methyl nonafluorobutyl ether, methyl nonafluoroisobutyl ether, ethyl nonafluorobutyl ether, ethyl nonafluoroisobutyl ether, 1,1,2,2-tetrafluoroethyl-2,2,2-trifluoroethyl Ether (also known as 1,1,2,2-tetrafluoro-1- (2,2,2-trifluoroethoxy) ethane, HFE-347pc-f), 1,1,1,2,2,3,4 5,5,5-Decafluoro-3-methoxy-4- (trifluoromethyl) pentane, 1,1,1,2,3,3-hexafluoro-4- (1,1,2,3,3)
  • the component (b10) is one or more selected from the group consisting of methyl nonafluorobutyl ether, methyl nonafluoroisobutyl ether and 1,1,2,2-tetrafluoroethyl-2,2,2-trifluoroethyl ether. There may be.
  • 3 ⁇ (trademark) Novec (trademark) 7100 high-performance liquid 3 ⁇ (trademark) Novec (trademark) 7200 high-performance liquid, 3 ⁇ (trademark) Novec (trademark) 7300 high-performance liquid.
  • 3 ⁇ (trademark) Novec (trademark) 7000 high-performance liquid manufactured by 3M Japan Co., Ltd.
  • Asahiclean AE3000 manufactured by AGC Co., Ltd.
  • Hydrocarbon ⁇ (B11) The hydrocarbon is composed of only carbon and hydrogen, may be linear or branched, may be cyclic or acyclic, and may have a carbon-carbon double bond. It is a hydrogen-based solvent.
  • the components (b11) include hexane, isohexane, cyclohexane, normalheptane, isoheptane, cycloheptane, normaloctane, isooctane, nonane, isononan, decane, methylcyclohexane, ethylcyclohexane, limonene, 2-methyl-2-butene, 2-.
  • Methyl-1-pentene 2-methyl-2-pentene, 3-ethyl-2-butene, 2,3-dimethyl-2-butene, 2,4,4-trimethyl-1-pentene, 2,4,4- Examples thereof include trimethyl-2-pentene, 2,2,4,6,6-pentamethylheptane, isododecane, isoparaffins, naphthenes, aromatic hydrocarbons and the like.
  • the hydrocarbon solvent may be a synthetic product.
  • (b12) chlorinated hydrocarbons (excluding (b6) chloroolefins, (b7) hydrofluoroolefins and (b11) hydrocarbons)
  • the (b12) chlorinated hydrocarbon (excluding (b6) chloroolefin, (b7) hydrofluoroolefin and (b11) hydrocarbon) contains a chlorine atom and a carbon atom, and may contain a hydrogen atom. It is a solvent.
  • the component (b12) include methylene chloride and the like.
  • Combination of sulfuric acid with one or more selected from the group consisting of (b13) alkylbenzene sulfonic acid and its salts
  • the combination of sulfuric acid and one or more selected from the group consisting of (b13) alkylbenzene sulfonic acid and its salt is a combination of (b13-1) alkylbenzene sulfonic acid and / or its salt and (b13-2) sulfuric acid.
  • the alkyl group of alkylbenzene sulfonic acid in the component (b13-1) is linear or branched. Therefore, the component (b13-1) specifically includes a salt of linear alkylbenzene sulfonic acid, a salt of linear alkylbenzene sulfonic acid, a salt of branched chain alkylbenzene sulfonic acid and a salt of branched chain alkylbenzene sulfonic acid. From the viewpoint of further increasing the solubility in a resin or the like, the number of carbon atoms of the alkyl group may be 6 to 20, 6 to 16, 10 to 14, or 12 to 14. May be.
  • Examples of the cation source for forming the salt of alkylbenzene sulfonic acid include alkali metals such as lithium, sodium and potassium; alkaline earth metals such as magnesium and calcium; alkanolamines such as monoethanolamine, diethanolamine and triethanolamine; ammonium ions and the like. Can be mentioned. From the viewpoint of further increasing the solubility in a resin or the like, the salt of alkylbenzene sulfonic acid may be one or more selected from the group consisting of an alkali metal salt of alkylbenzene sulfonic acid and an alkaline earth metal salt of alkylbenzene sulfonic acid. ..
  • the component (b13-1) contains one or more selected from the group consisting of a linear alkylbenzene sulfonic acid, a salt of a linear alkylbenzene sulfonic acid, a branched chain alkylbenzene sulfonic acid and a salt of a branched chain alkylbenzene sulfonic acid.
  • the number of carbon atoms of the alkyl group may be 6 to 20 (6 to 16, 10 to 14, or 12 to 14).
  • the component (b13-2) is sulfuric acid, and when combined with the component (b13-1), it is a component that further enhances the solubility in a resin or the like.
  • the sulfuric acid may be free sulfuric acid.
  • component (B) Further components may be one kind or a combination of two or more kinds, respectively.
  • the component (B) may be a combination of one or more types of (b6) chloroolefin and one or more types of (b10) hydrofluoroether.
  • the component (B) may be a combination of one kind or two or more kinds of (b2) ether and one kind or two or more kinds of (b8) hydrobromocarbon.
  • the additive (C) is a component other than the component (B) and is not particularly limited as long as it is a component commonly used in the field of solvent composition.
  • Examples of the (C) additive include one or more selected from the group consisting of water, an ultraviolet absorber, an antioxidant, a polymerization inhibitor, a rust inhibitor, an antifoaming agent, a surfactant, a chelating agent and the like. ..
  • Ultraviolet absorbers and antioxidants are components that improve the stability of solvent compositions during long-term storage and the like.
  • the ultraviolet absorber include a benzotriazole-based ultraviolet absorber, a benzophenone-based ultraviolet absorber, and a hindered amine-based ultraviolet absorber.
  • the antioxidant include phenol-based antioxidants, amine-based antioxidants, sulfur-based antioxidants, and phosphorus-based antioxidants.
  • Phenolic antioxidants include 2,6-di-t-butyl-4-methylphenol, triethylene glycol-bis [3- (3-t-butyl-5-methyl-4-hydroxyphenyl) propionate], 1 , 6-Hexanediol-bis [3- (3,5-di-t-butyl-4-hydroxyphenyl) propionate], 2,4-bis- (n-octylthio) -6- (4-hydroxy-3, 5-di-t-butylanilino) -1,3,5-triazine, pentaerythrityl-tetrakis [3- (3,5-di-t-butyl-4-hydroxyphenyl) propionate], 2,2-thio- Diethylenebis [3- (3,5-di-t-butyl-hydroxyphenyl) propionate], octadodecyl-3- [3,5-di-t-butyl-4-hydroxyphenyl] propionate], N, N-
  • Amine-based antioxidants include alkylated diphenylamine, tris- (3,5-di-t-butyl-4-hydroxybenzyl) -isocyanurate, N, N-di-sec-butyl-p-phenylenediamine, p- Examples thereof include phenylenediamine derivatives, 1,3,5-tris (4-t-butyl-3-hydroxy-2,6-dimethyl) isocyanurate.
  • Sulfur-based antioxidants include 2,4-bis [(octylthio) methyl] -o-cresol, dilauryl-3,3-thiodipropionate, dimyristyl-3,3-diodipropionate, disstearyl-3, 3-thiodipropionate, pentaerythrityltetrakis (3-laurylthiopropionate), ditridecyl-3,3-thiodipropionate, 2-mercaptobenzimidazole, bis [2-methyl-4- (3-n) -Alkylthiopropionyloxy) -5-t-butylphenyl] sulfide and the like can be mentioned.
  • Examples of the phosphorus-based antioxidant include tris-nonylphenylphosphine, triphenylphosphine, tris (2,4-di-t-butylphenyl) phosphite, and tris (isodecyl) phosphite.
  • the chelating agent examples include aminocarboxylic acid-based chelating agents, and hydroxyethylaminoacetic acid, hydroxyethyliminodiacetic acid, ethylenediaminetetraacetic acid, salts thereof and the like are preferable.
  • Examples of the rust preventive agent include cyclohexylamine, dicyclohexylamine and N, N-bis (2-hydroxyethyl) -N-cyclohexylamine.
  • Examples of the surfactant include nonionic surfactants, higher alcohol ethylene oxide adducts, alkylphenol ethylene oxide adducts, fatty acid ethylene oxide adducts, higher alkylamine ethylene oxide adducts, fatty acid esters of sorbitol and sorbitan, and sho.
  • Sugar fatty acid esters, silicone-based surfactants, fluorine-based surfactants, and the like are preferable.
  • Additives other than the above-mentioned components are not particularly limited as long as they are components commonly used in the field of solvent compositions, and can be used as appropriate.
  • the additive may be one kind or a combination of two or more kinds, respectively.
  • the content of each component with respect to a total of 100 parts by weight of the component (A), the component (B) and the component (C) is as follows.
  • the content of the component (A) is preferably 3 parts by weight or more and 100 parts by weight or less, more preferably 10 parts by weight or more and 90 parts by weight or less, and preferably 15 parts by weight or more and 80 parts by weight or less. It is more preferably 30 parts by weight or more and 70 parts by weight or less.
  • the content of the component (A) may be 10 parts by weight or more and 100 parts by weight or less, 15 parts by weight or more and 80 parts by weight or less, and 30 parts by weight or more and 100 parts by weight or less. May be good.
  • the content of the component (B) is preferably 95 parts by weight or less, more preferably 90 parts by weight or less, further preferably 70 parts by weight or less, and particularly preferably 50 parts by weight or less. preferable.
  • the content of the component (B) is preferably 5 parts by weight or more, more preferably 8 parts by weight or more, further preferably 20 parts by weight or more, and more preferably 50 parts by weight or more. Is particularly preferable.
  • the content of the component (C) is preferably 20 parts by weight or less, more preferably 10 parts by weight or less, further preferably 5 parts by weight or less, and particularly preferably 1 part by weight or less. preferable.
  • the total content of the component (A), the component (B) and the component (C) may be 70 to 100 parts by weight, and may be 80 to 80 parts by weight. It may be 100 parts by weight or 90 to 100 parts by weight. Further, when the total amount of the solvent composition is 100 parts by weight, the total content of the component (A), the component (B) and the component (C) may be 70 parts by weight or more and less than 100 parts by weight. , 80 parts by weight or more and less than 100 parts by weight, or 90 parts by weight or more and less than 100 parts by weight. Within such a range, the effect as a solvent composition is more excellent.
  • the solvent composition has (A).
  • the content of each component with respect to a total of 100 parts by weight of the component (B) and the component (C) is the content of each component when the total amount of the solvent composition is 100 parts by weight.
  • the solvent composition contains the component (B) other than the specific component (for example, (b2) to (b13). ) Ingredient) may or may not be contained.
  • the specific component is the component (b1) and the component (B) other than the specific component is one or more selected from the group consisting of the components (b2) to (b13)
  • the total amount of the solvent composition is 100 parts by weight
  • the total content of the component (A), the component (b1) and the component (C) is 70 parts by weight
  • the components (b2) to (b13) are used.
  • the residue including one or more selected from the group may be 30 parts by weight.
  • the component (C) is limited to a specific component.
  • Further components preferably include (b9) hydrofluorocarbons and / or (b10) hydrofluoroethers. Some (b9) hydrofluorocarbons and some (b10) hydrofluoroethers are not VOC-applicable under US EPA and Chinese regulations GB38508-2020, and are solvents containing components (b9) and (b10). The composition is more environmentally friendly.
  • Such VOC non-applicable (b9) components include 1,1,1,3,3-pentafluorobutane, 1,1,1,2,2,3,4,5,5-deca. Fluoropentane can be mentioned.
  • the component (b10) that is not applicable to VOC 1,1,2,2-tetrafluoroethyl-2,2,2-trifluoroethyl ether, methyl nonafluorobutyl ether, methyl nonafluoroisobutyl ether, ethyl nona Examples thereof include fluorobutyl ether and ethyl nonafluoroisobutyl ether.
  • the additional component is (b9) a hydrocarbon and (b3) an ester (excluding (b2) ether), (b4) an alcohol ((b2).
  • the solvent composition contains the component (A), optionally contains the component (B) and / or the component (C), and the content of the component (A) is 100 parts by weight when the total amount of the solvent composition is 100 parts by weight. 3.
  • the content may be 3 parts by weight or more and 100 parts by weight or less, the content of the component (B) may be 95 parts by weight or less, and the content of the component (C) may be 20 parts by weight or less.
  • the content of each component may be 20 parts by weight or less with respect to a total of 100 parts by weight of the component (A), the component (B) and the component (C). It may be 5 parts by weight or less, 5 parts by weight or less, or 1 part by weight or less.
  • the components (B) are (b1) nitro compound, (b5) amide compound, (b6-1) hydrochloroolefin, (b7) hydrofluoroolefin, (b8) hydrobromocarbon, (b9) hydrofluorocarbon and (b10). It may be one or more selected from the group consisting of hydrofluoroethers.
  • the component (B) is at least one selected from the group consisting of (b8) hydrobromocarbon and (b6-1) hydrochloroolefin, where (b8) is 1-bromopropane and (b6). -1) may be trans-1,2-dichloroethylene.
  • the content of the component (b8) is 5 to 90 with respect to a total of 100 parts by weight of the component (A), the component (B) and the component (C). It may be a part by weight or 20 to 90 parts by weight.
  • the component (B) is (b6-1) hydrochloroolefin
  • the content of the component (b6-1) may be 5 to 90 parts by weight or 55 to 90 parts by weight.
  • the component (B) is from the group consisting of (b8) hydrobromocarbon, (b1) nitro compound, (b2-2) cyclic ether (excluding (b2-3) epoxide) and (b2-3) epoxide.
  • (B8) may be 1-bromopropane, including one or more selected species.
  • the solvent composition essentially comprises component (A) and component (b8) which is 1-bromopropane, and optionally contains component (b1), component (b2-2) and component (b2-3). Includes one or more selected from the group consisting of.
  • the content of the component (A) may be 10 to 95 parts by weight with respect to a total of 100 parts by weight of the component (A), the component (B) and the component (C), and the component (b8).
  • the content of each of the components (b1), (b2-2) and (b2-3) may be 5 to 90 parts by weight, and the content of each of the components (b1), (b2-2) and (b2-3) is 0.01 to 5.0 parts by weight. May be.
  • the component (B) comprises (b8) hydrobromocarbon which is 1-bromopropane and / or (b6-1) hydrochloroolefin which is trans-1,2-dichloroethylene
  • the component (B) further comprises.
  • (B2-1) may contain acyclic ether, and (b2-1) may be propylene glycol monomethyl ether.
  • the component (A), the component (B) and the component (C) may be 10 parts by weight or more (for example, 10 to 90 parts by weight) or 25 parts by weight or more with respect to 100 parts by weight in total (b8).
  • the content of the component may be 5 to 80 parts by weight, 25 to 60 parts by weight, and the content of the (b2-1) component may be 5 to 70 parts by weight. It may be 6 to 70 parts by weight, 8 to 70 parts by weight, or 14 to 50 parts by weight.
  • the component (b2-1) When the content of the component (b2-1) is 8 parts by weight or more, the component (b8) and (b8) component and (b8) component and ( b2-1)
  • the total content of the components may be 18 parts by weight or more.
  • the solvent composition further contains one or more selected from the group consisting of the component (b1), the component (b2-2) and the component (b2-3), the component (A), the component (B) and ( The content of each of the components (b1), (b2-2) and (b2-3) is 0.01 to 5.0 parts by weight with respect to 100 parts by weight of the total component C). There may be.
  • the solvent composition contains (b6-1) hydrochloroolefin which is trans-1,2-dichloroethylene and (b2-1) acyclic ether which is propylene glycol monomethyl ether
  • the components (A) and (B) and, with respect to a total of 100 parts by weight of the component (C) the content of the component (A) may be 10 parts by weight or more (for example, 10 to 90 parts by weight), or 15 to 35 parts by weight.
  • the content of the component (b6-1) may be 5 to 80 parts by weight or 25 to 60 parts by weight, and the content of the component (b2-1) may be 5 to 70 parts by weight. It may be a part by weight, 6 to 70 parts by weight, 8 to 70 parts by weight, or 14 to 50 parts by weight.
  • the total content of the component (b6-1) and the component (b2-1) is 13 parts by weight or more with respect to 100 parts by weight of the total of the component (A), the component (B) and the component (C). There may be.
  • the component (B) is a (b5) amide compound, and (b5) is at least one selected from the group consisting of N-methyl-2-pyrrolidone and 3-methoxy-N, N-dimethylpropanamide. May be good.
  • the content of the component (A) may be 10 to 95 parts by weight with respect to a total of 100 parts by weight of the component (A), the component (B) and the component (C), and the component (b5).
  • the content of the above may be 5 to 90 parts by weight or 30 to 85 parts by weight.
  • the component (B) may be a combination of sulfuric acid and one or more selected from the group consisting of (b13) alkylbenzene sulfonic acid and a salt thereof. Further, when the component (B) contains the component (b13), the component (B) may further contain one or more selected from the group consisting of (b9) hydrofluorocarbon and (b10) hydrofluoroether. good.
  • the content of the component (A) may be 10 to 99 parts by weight with respect to a total of 100 parts by weight of the component (A), the component (B) and the component (C), and the component (b13).
  • the content of the above may be 1 to 90 parts by weight, 2 to 50 parts by weight, or 2 to 20 parts by weight.
  • the content of the component (b13) may be 15 to 40 parts by weight. Further, the contents of the component (b13-1) and the component (b13-2) with respect to a total of 100 parts by weight of the component (b13-1) and the component (b13-2) are not particularly limited, and (b13-1).
  • the component may be 85 parts by weight or more and 99.99 parts by weight or less, the (b13-2) component may be 0.01 parts by weight or more and 15 parts by weight or less, and the (b13-1) component may be 90 parts by weight. It may be 99.9 parts by weight or less, and the component (b13-2) may be 0.1 to 10 parts by weight or less.
  • the solvent composition contains at least one selected from the group consisting of the component (b9) and the component (b10) in addition to the component (b13), the component (A), the component (B) and the component (C) are included.
  • the content of the component (A) may be 20 to 80 parts by weight, and the content of the component (b13) may be 10 to 40 parts by weight with respect to a total of 100 parts by weight of the components. , 20 to 30 parts by weight, and the total content of the component (b9) and the component (b10) may be 5 to 50 parts by weight, or 25 to 40 parts by weight.
  • the solvent composition in which the component (A) is 14.44 parts by weight and the methyl acetate is 83.07 parts by weight may be removed, and the component (A) is 14.44 parts by weight.
  • the solvent composition in which methyl acetate is 83.07 parts by weight and cyclohexane is 2.48 parts by weight may be removed.
  • the method for producing the solvent composition is arbitrary.
  • the raw material component contained in the solvent composition is produced by appropriately selecting a known method, for example, by performing one or more means selected from the group consisting of stirring, mixing, dissolution and dispersion. Can be done.
  • the solvent composition can be used as a cleaning agent, a cleaning aerosol composition, a dissolving agent for a cured resin, an adhesive for a cured resin, and a coating agent for a resin.
  • the solvent composition is excellent in the solubility of oil, flux and / or uncured resin
  • the object to be cleaned to which one or more selected from the group consisting of oily stains, oil, flux and uncured resin is attached.
  • Can be used as a cleaning agent for cleaning. Therefore, the present invention also relates to the use as a cleaning agent for cleaning an object to be cleaned to which one or more selected from the group consisting of oily stains, oil, flux and uncured resin is attached to the solvent composition. ..
  • Oil examples include mineral oil, vegetable oil, animal oil, heavy oil, wax, silicone oil, fluorine oil and the like. These oils may be used as, for example, cutting oil, pressing oil, drawing oil, heat treatment oil, rust preventive oil, lubricating oil, metalworking oil, grease, asphalt, and water-soluble oil.
  • the mineral oil is not particularly limited, and the commercially available product includes pulley SF oil (manufactured by Idemitsu Kosan Co., Ltd.).
  • vegetable oils include olive oil, flaxseed oil, millet oil, sesame oil, safflower oil, soybean oil, castor oil, cottonseed oil, palm oil, corn oil and dehydrated castor oil.
  • the fatty acids constituting the vegetable oil are saturated or unsaturated fatty acids of C12 to C18, and specifically, lauric acid, myristic acid, palmitic acid, stearic acid, oleic acid, linoleic acid, linolenic acid, and eleostearic acid. And so on.
  • animal oils include fish oil, whale oil, lard, and beef tallow.
  • heavy oil include asphaltene and the like.
  • resin include pitch, pine fat and the like.
  • wax include plant-based, animal-based, petroleum-based, and synthetic hydrocarbon-based waxes, and specific examples thereof include paraffin wax.
  • Silicone oil is a silicone oil that is a linear polymer composed of siloxane bonds, and mainly has a carboxyl group, an amino group, a polyether group, an epoxy group, or the like on the side chain or the terminal of dimethyl silicone oil or methyl phenyl silicone oil. Other organic groups may be introduced. Specific examples of such silicone oil include dimethylpolysiloxane, methylphenylpolysiloxane, octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, polyoxyethylene-methylpolysiloxane, and the like. Examples of such silicone oils include KF-96L-2CS and KF-6012 manufactured by Shin-Etsu Chemical Co., Ltd. as commercially available products.
  • Fluorine oil is a substance in which a part or all of hydrogen atoms in a polyalkyl ether compound is replaced with fluorine, and may contain halogens such as chlorine and bromine, and additional atoms such as phosphorus, sulfur, and nitrogen. ..
  • Commercially available products of fluorine oil include, for example, von Bryn Y-LVAC, Y-HVAC, Y04, and YR manufactured by Solvaisolexis Co., Ltd .; BARRIERTA J100 fluid, Barrierta J25 fluid, and Varierta manufactured by NOK Kluber Co., Ltd.
  • Examples thereof include J400 fluid, Varierta J25V, Varierta SJ07, Varierta SJ15, and Varierta SJ30; Critex 1506 and Critex 1514 manufactured by DuPont Co., Ltd .; and Demnum S-20 manufactured by Daikin Industries, Ltd.
  • Water-soluble oils are roughly classified into emulsion type, soluble type, and solution type.
  • the emulsion type contains water-insoluble oil such as mineral oil and fatty oil and a surfactant as main components, and forms a milky white emulsion when diluted with water.
  • the soluble type also contains water-insoluble oil and surfactant, but becomes transparent to translucent when diluted with water.
  • the solution type is mainly composed of water-soluble inorganic salts and the like, and becomes transparent when diluted with water.
  • silicone oil in which silicone oil, a surfactant and water are mixed.
  • the flux examples include rosin-based flux.
  • the rosin-based flux is an inactive rosin flux containing rosins (resinic acid containing abietic acid as a main component) and rosins such as modified rosin as main components; the rosins and an inorganic acid salt of an amine compound (for example, hydrochloride). , Sulfate) and an active rosin flux containing one or more activators selected from the group consisting of organic acids as main components.
  • the inorganic acid salt of the amine compound include triethanolamine hydrochloride, triethylenetetraamine hydrochloride, cyclohexylamine hydrochloride, aniline hydrochloride and the like.
  • the organic acid include carboxylic acids (including dicarboxylic acids) such as succinic acid, adipic acid, glutaric acid, sebacic acid and maleic acid; and oxyacids (hydroxycarboxylic acids).
  • the flux may be provided in the form of cream solder in which a metal for soldering and rosin flux are integrated.
  • the cream solder is a composition containing a solder alloy powder, a resin, an activator, an antioxidant, a chixo agent, and a solvent, and is composed of a so-called metal powder and a flux component.
  • the resin in the uncured resin is not particularly limited, and includes acrylic resin, polycarbonate resin, acrylonitrile / butadiene / styrene resin, silicone resin, polyamide resin, urethane resin, polyacetal resin, epoxy resin styrol resin, polyvinyl chloride resin and the like. Can be mentioned.
  • acrylic resin examples include compounds having an acryloyl group and / or a methacryloyl group, and specific examples thereof include methyl (meth) acrylate and 2-hydroxyethyl (meth) acrylate.
  • (meth) acrylate means at least one of acrylate and methacrylate.
  • the acrylic resin preferably does not have a fluorine atom, and particularly preferably does not have a halogen atom.
  • Additives to be blended in acrylic resin include curing agents, curing accelerators, fillers, stabilizers, plasticizers, lubricants, flame retardants, flame retardant aids, antistatic agents, colorants, antistatic agents, and ⁇ Examples include a dynamic improver, an impact resistance improver, a reaction diluent and the like.
  • Acrylic resin has good workability and excellent transparency, so the cured product of acrylic resin is used for windshield, windows of aircraft, ships, automobiles, water tanks, lenses, lighting equipment, displays, signboards, etc. ..
  • Polycarbonate resin is a type of thermoplastic.
  • Additives to be blended in polycarbonate resin include curing agents, curing accelerators, fillers, stabilizers, plasticizers, lubricants, flame retardants, flame retardant aids, antistatic agents, colorants, charge-imparting agents, and ⁇ Examples include a dynamic improver, an impact resistance improver, a reaction diluent and the like.
  • the cured product of polycarbonate resin is widely used for members of automobiles and the like, and is used for roofs, headlamp lenses and the like.
  • the acrylonitrile-butadiene-styrene resin is an acrylonitrile-styrene-based copolymer that is a copolymer of acrylonitrile and styrene in which polybutadiene, which is a rubbery polymer, is dispersed, and contains three components of acrylonitrile, butadiene, and styrene. Mainly.
  • Additives to be added to acrylonitrile, butadiene, and styrene resins include curing agents, curing accelerators, fillers, stabilizers, plasticizers, lubricants, flame retardants, flame retardants, antistatic agents, colorants, and chargeability.
  • Examples thereof include an additive, a mobilization improver, an impact resistance improver, a reaction diluent and the like.
  • the cured product of acrylonitrile, butadiene, and styrene resin is widely used for interior and exterior members of automobiles and the like, and is used for wheel caps, wheel covers, dashboards, and the like.
  • the silicone resin is a highly condensate of an organic silicon compound and has a repeating structure of dimethylsiloxane or methylphenylsiloxane.
  • Additives to be blended in silicone resin include curing agents, curing accelerators, fillers, stabilizers, plasticizers, lubricants, flame retardants, flame retardant aids, antistatic agents, colorants, charge-imparting agents, and ⁇ Examples thereof include additives such as a dynamic improver, an impact resistance improver, and a reaction diluent.
  • the cured product of the silicone resin is used as an adhesive, a coating agent, or the like.
  • the polyamide resin is a copolymer having an amide bond, and may be synthesized by a polycondensation reaction of ⁇ -amino acid or a copolymerization reaction of diamine and a dicarboxylic acid.
  • the polyamide resin may be aliphatic or aromatic.
  • Additives to be added to the polyamide resin include curing agents, curing accelerators, fillers, stabilizers, plasticizers, lubricants, flame retardants, flame retardant aids, antistatic agents, colorants, charge-imparting agents, and ⁇ . Examples include a dynamic improver, an impact resistance improver, a reaction diluent and the like.
  • the cured product of the polyamide resin is used for automobile parts such as engine covers, industrial valves, filaments and the like.
  • urethane resin examples include reaction products of diisocyanates such as tolylene diisocyanate (TDI) and diphenylmethane diisocyanate (MDI) and polyols such as polypropylene glycol.
  • TDI tolylene diisocyanate
  • MDI diphenylmethane diisocyanate
  • polyols such as polypropylene glycol.
  • Additives to be blended in urethane resin include curing agents, curing accelerators, emulsifiers, foaming agents, stabilizers, plasticizers, flame retardants, antistatic agents, colorants, oscillating agents, and impact resistance improvements. Agents and the like can be mentioned.
  • the cured product of urethane resin is used as a heat insulating material, a coating agent for electronic substrates, and the like.
  • the polyacetal resin is a copolymer having an oxymethylene (-CH 2 O-) structure as a unit structure, and may contain an oxyethylene unit (-CH 2 CH 2 O-) unit.
  • Additives to be added to polyacetal resins include curing agents, curing accelerators, fillers, stabilizers, plasticizers, lubricants, flame retardants, flame retardant aids, antistatic agents, colorants, antistatic agents, and ⁇ Examples include a dynamic improver, an impact resistance improver, a reaction diluent and the like.
  • the cured product of polyacetal resin is used for gears, bearings, pump parts and the like.
  • epoxy resin bisphenol A type epoxy resin, bisphenol F type epoxy resin, bisphenol AD type epoxy resin, polyhydric alcohol polyglycidyl ether, polybasic acid polyglycidyl ester, 3,4-epoxycyclohexyl-3', 4 '-Epoxycyclohexanecarboxylates, vinylcyclohexendiepoxides, cresol novolac type epoxy resins, and epoxy resins with a hydantin ring can be mentioned.
  • Additives to be added to epoxy resins include curing agents, curing accelerators, fillers, stabilizers, plasticizers, lubricants, flame retardants, flame retardant aids, antistatic agents, colorants, charge-imparting agents, and ⁇ Examples include a dynamic improver, an impact resistance improver, a reaction diluent and the like.
  • the epoxy resin curing agent may be any as long as it is usually used as an epoxy resin curing agent, for example, novolak such as phenol novolac, biphenol type novolak, and bisphenol A type novolak, and phthalic anhydride.
  • Acid anhydrides such as pyromellitic anhydride and benzophenone tetracarboxylic acid anhydride, amines such as diaminodiphenylmethane, diaminodiphenylsulfone, metaphenylenediamine, and hexamethylenetetramine, and amide resins such as polyamideamine.
  • the curing accelerator include tertiary amines and organic phosphorus compounds.
  • the cured product of the epoxy resin is used as an adhesive, a potting agent for an electronic substrate, or the like.
  • Styrene resin is a polymer containing styrene as a monomer, and its cured product is also called polystyrene.
  • the cured foam of the styrene resin is also referred to as Styrofoam.
  • Additives to be blended in styrene resin include foaming agents, curing agents, curing accelerators, fillers, stabilizers, plasticizers, lubricants, flame retardants, flame retardant aids, antistatic agents, colorants, and antistatic agents. Examples thereof include agents, mobilization improvers, impact resistance improvers, reaction diluents and the like.
  • the cured product of styrene resin is used for automobile lamp lenses, covers and the like.
  • the polyvinyl chloride resin is a homopolymer of vinyl chloride or a copolymer of vinyl chloride and a further vinyl monomer.
  • Additives to be blended in polyvinyl chloride resin include curing agents, curing accelerators, fillers, stabilizers, plasticizers, lubricants, flame retardants, flame retardant aids, antistatic agents, colorants, and antistatic agents. , Antistatic improver, impact resistance improver, reaction diluent and the like.
  • the cured product of polyvinyl chloride resin is used for building materials such as pipes and flooring materials.
  • Oily stains include oil stains, flux stains, and uncured resin stains.
  • the oil, flux and uncured resin that are the raw materials for oily stains are as described above.
  • the oily stains include non-polar oily stains, oily stains due to polar components, and oily stains due to a plurality of components having different polarities, depending on the polarity of the oil.
  • the flux stain includes rosin which is a flux component, an inorganic acid salt of an amine compound, an organic acid, and a component in which the component is partially altered or carbonized by reflow at a high temperature.
  • the stains on the cream solder include stains on the flux component and metal powder.
  • the resin stains include non-polar resin stains, oily stains due to polar components, and oily stains due to a plurality of components having different polarities, depending on the polarity of the resin component and the components used in combination.
  • the cleaning aerosol composition contains a solvent composition and a propellant gas. Therefore, the present invention also relates to the use of an aerosol composition containing a solvent composition and an injection gas as a cleaning aerosol composition.
  • the aerosol composition maintains its state as a solution without volatilizing the solvent composition immediately after spraying. Then, the aerosol composition after injection becomes fine droplets and does not spread over a wide range, but the atomized solvent composition can be concentrated and delivered to a narrow range. That is, the solvent composition can be applied to a portion to be washed from a long distance. Then, it is possible to prevent the solvent composition from coming into contact with the base material of the object to be cleaned, and to efficiently clean the metal portion of the object to be cleaned.
  • the injection gas examples include one or more selected from the group consisting of compressed air, N 2 , argon, CO 2 , and LPG.
  • the form of the injected gas is not particularly limited, and examples thereof include a form of a liquefied gas and a form of a compressed gas. From the viewpoint of suppressing the rapid volatilization of the solvent composition, it is preferable that the solvent composition is at least one selected from the group consisting of compressed air, N 2 , argon and CO 2 .
  • the method for producing the aerosol composition for cleaning is not particularly limited, and for example, a method of filling an aerosol composition in which a solvent composition and a liquid jet gas are mixed into a pressure-resistant can to make the aerosol composition into an aerosol, or a method of filling an aerosol composition into a container. Examples thereof include a method in which compressed air is filled in a container using an air compressor or the like after being added to (for example, a pail can) to aerosolize the solvent composition.
  • the description in JP-A-2018-105723 can be referred to.
  • the cleaning method using the solvent composition includes contacting the solvent composition with the object to be cleaned. Oily stains, oil, flux and / or uncured resin adhere to the substrate of the object to be cleaned. In the cleaning method, by bringing the solvent composition into contact with the object to be cleaned, oily stains, oils, fluxes and / or uncured resins adhering to the substrate are removed from the substrate. When the oil-based stain contains solid stains such as dust and dirt, the solid stain can be removed at the same time as the oil-based stain is removed.
  • the base material is not particularly limited, and examples thereof include metal, fiber, glass, pottery, and plastic.
  • Metals include silver, zinc, nickel, iron, aluminum, copper, manganese, magnesium, stainless steel, and aluminum alloys (alloys of aluminum and one or more metals consisting of copper, manganese, silicon, magnesium, zinc, and nickel). And so on.
  • the aluminum alloy may be die-cast aluminum, and examples thereof include ADC12 and ADC14.
  • the plastic include PET resin (polyethylene terephthalate resin), epoxy resin, acrylic resin, polycarbonate resin, silicone resin, ABS resin (acrylonitrile, butadiene, styrene resin) and the like.
  • the base material may be plastic as long as the above-mentioned oily stains, oil, flux or resin are removed from the base material. Specific examples of the base material include an apparatus for obtaining a cured product of the resin.
  • the method for bringing the solvent composition into contact with the object to be cleaned is not particularly limited, and for example, hand-wiping cleaning, immersion cleaning (liquid phase cleaning), spray cleaning (including spraying with a cleaning aerosol composition), and cleaning.
  • shower cleaning, ultrasonic cleaning, steam cleaning (gas phase cleaning) and combinations thereof include hand wiping cleaning, immersion cleaning, steam cleaning, spray cleaning (including spray cleaning by spraying an aerosol composition for cleaning), and A combination of immersion cleaning and steam cleaning is preferred.
  • Hand-wiping cleaning is usually performed by rubbing a paper, cloth, etc. impregnated with the composition by hand while contacting an area with oily stains and / or oil, or a paper, cloth, etc. impregnated with the composition.
  • Spray cleaning by spraying the cleaning aerosol composition is performed by spraying the cleaning aerosol composition as an aerosol on an area to which oily stains and / or oil are attached.
  • step (1A) a step of immersing the object to be cleaned in the solvent composition and a step.
  • the step (1A) is a step of immersing the object to be cleaned in the solvent composition.
  • the object to be cleaned comes into contact with the solvent composition.
  • the immersion cleaning time is not particularly limited as long as it is a time during which oily stains and / or oil adhering to the object to be cleaned can be washed and removed. Oily stains and / or oil are removed from the object to be cleaned by the step (1A).
  • the step (1A) may be composed of a plurality of washing tanks.
  • the step (1B) is a step of generating steam containing the component (A) from the solvent composition and bringing the object to be cleaned into contact with the generated vapor containing the component (A). If the solvent composition is an azeotropic composition, the "steam containing (A)" is the vapor of the solvent composition. If the solvent composition is not an azeotropic composition, the solvent composition is heated so as to generate vapor containing at least the component (A).
  • steam cleaning is performed by bringing the object to be cleaned into contact with steam generated from the solvent composition.
  • the steam cleaning time is not particularly limited, but can be 1 second or more and 60 minutes or less. As a result, the solvent composition and the dirt component adhering to the object to be cleaned are exchanged with the vapor phase component. Further, in the step (1B), since the object to be cleaned and the component (A) come into contact with each other, rinsing (steam rinsing) is performed by the step of steam cleaning.
  • a cleaning device having a steam tank can be mentioned.
  • the cleaning agent used in the cleaning tank and the cleaning agent used in the steam tank may be the same or different.
  • the vapor of the cleaning agent may be generated from the washing tank.
  • the washing tank also serves as a steam tank.
  • the solvent composition contained in the washing tank is heated so that at least the component (A) is in a boiling state.
  • the cleaning time corresponding to the contact time of the solvent composition and the object to be cleaned is not particularly limited as long as it is a time during which oily stains and / or oil can be removed from the substrate.
  • the washing time may be 10 seconds or more and 2 hours or less.
  • cleaning method and the cleaning system (cleaning device) used in the cleaning method other than the above will be described.
  • the cleaning system (cleaning apparatus) used in the cleaning method include a cleaning tank in which a cleaning agent is stored and an object to be cleaned is immersed, which is disclosed in JP-A-2008-163400 and JP-A-2015-217319.
  • examples thereof include a cleaning device having a steam tank for generating the steam of the cleaning agent.
  • a preferable cleaning system used for the cleaning method and a cleaning method using the cleaning system will be described.
  • the cleaning system 1 is a single-tank type cleaning machine.
  • the cleaning system 1 includes a boiling tank in which a cleaning agent is housed and an object to be cleaned is immersed and generates steam of the cleaning agent, and a recovery unit that liquefies and recovers the steam of the cleaning agent generated by the boiling tank.
  • a cleaning system including a water separator that separates water from the recovered liquid recovered by the recovery unit and extracts the cleaning agent.
  • the outline of the cleaning system 1 is shown in FIG.
  • the cleaning system 1 is preferably generated from a boiling tank (11 in FIG. 1) containing a cleaning agent (1 in FIG. 1) containing a component (A) and a component (B), and a boiling tank.
  • Water is separated from the recovery unit (for example, 21 and 22 in FIG. 1) for liquefying and recovering the steam of the cleaning agent (2 in FIG. 1) and the recovery liquid recovered by the recovery unit, and the cleaning is performed.
  • It is equipped with a water separator (23 in FIG. 1) that extracts the agent and supplies the extracted cleaning agent to the boiling tank.
  • the solid arrow indicates the flow of the cleaning agent.
  • the boiling tank is a tank for boiling and cleaning the object to be cleaned.
  • the boiling tank is sometimes called a vapor tank or a steam tank.
  • the boiling tank is provided with a heater (24 in FIG. 1) for maintaining the temperature above the temperature at which the vapor of the cleaning agent is generated (preferably above the boiling point of the cleaning agent).
  • the boiling tank may have an ultrasonic vibrator that gives ultrasonic vibration to the cleaning liquid.
  • a pump and a filter circuit can be installed in the boiling tank.
  • the recovery unit that liquefies and collects the vapor of the cleaning agent generated by the boiling tank.
  • the recovery unit is not particularly limited as long as it includes a means for liquefying the vapor of the cleaning agent and a means for supplying the liquefied component to the water separator.
  • the means for liquefying the vapor of the cleaning agent is not particularly limited, but a cooling pipe (21 in FIG. 1) is preferable.
  • the cooling pipe is a means for lowering the temperature of the vapor of the cleaning agent to liquefy it.
  • the number of turns of the cooling pipe is preferably 3 or more, more preferably 4 or more, further preferably 5 or more, and particularly preferably 6 or more.
  • the means for supplying the liquefied cleaning agent to the water separator is not particularly limited, but a gutter (22 in FIG. 1) is preferable.
  • the gutter is provided to supply the cleaning agent liquefied by a cooling pipe or the like to the water separator.
  • the liquid of the cleaning agent that is liquefied by means for liquefying the vapor of the cleaning agent and is supplied to the water separator is referred to as a recovery liquid.
  • the cleaning agent is extracted by a water separator described later and reused as a regenerating liquid.
  • the water separator is provided to separate water from the recovery liquid, extract the cleaning agent, and return it to the boiling tank.
  • the means for separating water by the water separator is not particularly limited as long as it can separate water from the recovered liquid and extract the cleaning agent, and examples thereof include specific gravity separation and membrane separation.
  • the water separator preferably extracts the cleaning agent by specific gravity separation.
  • Examples of the structure of the water separator when the recovery unit includes a cooling pipe and a gutter and the means for separating water by the water separator is specific gravity separation include those disclosed in Japanese Patent Application Laid-Open No. 2015-217319.
  • the cleaning system 1 may have a supply means for shower cleaning with a cleaning agent. After the object to be cleaned is boiled and / or steam-washed, the cleaning effect tends to be further improved by shower-washing with the composition and causing the composition to collide with the surface of the object to be cleaned.
  • the cleaning method using the cleaning system 1 includes the following steps: (1A) a step of immersing the object to be cleaned in a boiling tank and boiling and cleaning, and (1B) placing the object to be cleaned in a steam area generated from the boiling tank. And includes a step of steam cleaning.
  • the step (1A) is a step of immersing the object to be washed in a boiling tank and boiling and washing.
  • the object to be cleaned (S in FIG. 1) is moved from the position of S1 at the start of cleaning to the position of S2 and immersed in the cleaning agent.
  • the object to be cleaned comes into contact with the liquid of the composition.
  • the cleaning agent In the boiling tank, the cleaning agent is in a boiling state, that is, in boiling cleaning, the cleaning agent is heated by a heating means such as a heater.
  • the step (1B) is a step of placing the object to be cleaned in the steam area generated from the boiling tank and performing steam cleaning.
  • the object to be cleaned is moved from the position of S2 to the position of S4, which is the upper part of the boiling tank, and placed in the steam area.
  • the vapor area consists of the vapor of the cleaning agent.
  • steam cleaning is performed by bringing the object to be cleaned into contact with steam generated from the boiling tank.
  • the dirt component adhering to the object to be cleaned is replaced with the cleaning agent in the steam area.
  • rinsing steam rinsing
  • the object to be cleaned is moved to the position of S5 where the cleaning is completed, and the cleaning is completed.
  • the washing system 2 is a two-tank washing machine. It is generated by an ultrasonic cleaning tank that contains a cleaning agent containing the component (A) and the component (B) and the object to be cleaned is immersed and cleaned, a steam tank that generates steam of the cleaning agent, and a steam tank. It is a cleaning system including a recovery unit that liquefies and recovers the steam of the cleaning agent, and a water separator that separates water from the recovery liquid collected by the recovery unit and extracts the cleaning agent.
  • the outline of the cleaning system 2 is shown in FIG.
  • the cleaning system 2 preferably includes an ultrasonic cleaning tank (12 in FIG. 2) containing a cleaning agent set (1 in FIG. 2) and a steam tank containing a cleaning agent (3 in FIG. 2). (13 in FIG. 2), a recovery unit (for example, 21 and 22 in FIG. 2) that liquefies and recovers the steam of the cleaning agent (2 in FIG. 2) generated from the steam tank, and a recovery unit. It is provided with a water separator (23 in FIG. 2) that separates water from the recovered liquid recovered by the above method, extracts the cleaning agent, and supplies the extracted cleaning agent to the ultrasonic cleaning tank.
  • the cleaning system 2 corresponds to a cleaning system 1 further provided with an ultrasonic cleaning tank, except that the cleaning agent is returned from the water separator to the ultrasonic cleaning tank.
  • the solid arrow indicates the flow of the cleaning agent.
  • the steam tank in the cleaning system 2, including the preferable one, is as described above in the cleaning system 1. It is desirable that the ultrasonic cleaning tank is provided with an ultrasonic vibrator (25 in FIG. 2) that gives ultrasonic vibration. Further, although not shown, the ultrasonic cleaning tank may be provided with a heater for controlling the temperature of the composition. In the cleaning system 2, when the dirt removed from the object to be cleaned is a solid substance, a pump and a filter circuit may be installed in the ultrasonic cleaning tank for the purpose of avoiding the accumulation of the dirt.
  • the cleaning agent extracted by the water separator is supplied to the ultrasonic cleaning tank. Further, the liquid level of the ultrasonic cleaning tank is higher than the liquid level of the steam tank, and the cleaning liquid overflows from the ultrasonic cleaning tank to the steam tank.
  • the cleaning method using the cleaning system 2 includes the following steps: (2A) a step of immersing the object to be cleaned in an ultrasonic cleaning tank for ultrasonic cleaning, and (2B) steam generated from the steam tank for the object to be cleaned. Includes a step of placing in an area and cleaning with steam.
  • the step (2A) is a step of immersing the object to be cleaned (S in FIG. 2) in an ultrasonic cleaning tank and performing ultrasonic cleaning.
  • the frequency of the ultrasonic wave is not particularly limited and can be set as appropriate.
  • the step (2B) is a step of placing the object to be cleaned in the steam area generated from the steam tank and performing steam cleaning.
  • the object to be cleaned is moved from the position of S2 to the position of S4, which is the upper part of the steam tank, and placed in the steam area.
  • steam cleaning is performed by bringing the object to be cleaned into contact with steam generated from the boiling tank.
  • the conditions in the step (2B) are as described above in the step (1B), including the preferable ones. After that, the object to be cleaned is moved to the position of S5 where the cleaning is completed, and the cleaning is completed.
  • the washing system 3 is a three-tank washing machine.
  • An ultrasonic cleaning tank containing a cleaning agent containing the component (A) and the component (B) and immersing and cleaning the object to be cleaned, and an ultrasonic cleaning tank containing the cleaning agent and immersing and rinsing the object to be cleaned.
  • a rinse tank a steam tank that generates cleaning agent steam, a recovery unit that liquefies and recovers the cleaning agent steam generated from the steam tank, and a recovery unit that separates water from the recovery liquid recovered by the recovery unit. It is a cleaning system equipped with a water separator that extracts the cleaning agent and returns it to the rinse tank.
  • the outline of the cleaning system 3 is shown in FIG.
  • the cleaning system 3 preferably includes an ultrasonic cleaning tank (12 in FIG. 3) containing a cleaning agent (1 in FIG. 3) and a rinsing tank (4 in FIG. 3) containing a rinsing liquid (4 in FIG. 3). Liquefaction of the cleaning agent steam (2 in FIG. 3) generated from the steam tank (13 in FIG. 3) and the steam tank (13 in FIG. 3) containing the cleaning agent (3 in FIG. 3). Then, water is separated from the recovery unit (for example, 21 and 22 in FIG. 3) to be collected and the recovery liquid collected by the collection unit to extract the cleaning agent, and the extracted cleaning agent is used. It is equipped with a water separator (23 in FIG. 3) that supplies the rinse tank.
  • the cleaning system 3 corresponds to a cleaning system 2 further provided with a rinsing tank. In FIG. 3, the solid arrow indicates the flow of the cleaning agent.
  • the ultrasonic cleaning tank and steam tank in the cleaning system 3 are as described above in the cleaning system 1 and the cleaning system 2.
  • the rinsing tank is a tank for rinsing and cleaning the object to be cleaned.
  • the rinse solution is a cleaning agent.
  • the rinsing tank may be provided with an ultrasonic transducer or a heater for adjusting the temperature of the rinsing liquid. From the viewpoint of preventing the decrease of the rinsing liquid due to the generation of steam, the temperature of the rinsing liquid in the rinsing tank is preferably lower than the boiling point of the rinsing liquid. If the dirt removed from the object to be cleaned is solid, a pump and filter circuit may be installed in the rinse tank for the purpose of avoiding the accumulation of dirt.
  • the cleaning agent extracted by the water separator flows into the rinsing tank.
  • the liquid level of the rinsing tank is higher than the liquid level of the ultrasonic cleaning tank, and the rinsing liquid overflows from the rinsing liquid tank to the ultrasonic cleaning tank.
  • the liquid level of the ultrasonic cleaning tank is higher than the liquid level of the steam tank, so that the cleaning liquid overflows from the ultrasonic cleaning tank to the steam tank.
  • the cleaning method using the cleaning system 3 includes the following steps: (3A) a step of immersing the object to be cleaned in an ultrasonic cleaning tank for ultrasonic cleaning, and (3B) a step of immersing the object to be cleaned in a rinsing tank. , The step of rinsing and (3C) the step of placing the object to be cleaned in the steam area generated from the steam tank and performing steam cleaning.
  • the step (3A) is a step of immersing the object to be cleaned in an ultrasonic cleaning tank and performing ultrasonic cleaning.
  • the conditions in the step (3A), including those preferable, are as described above in the step (2A).
  • the step (3B) is a step of immersing the object to be cleaned in a rinsing tank and rinsing it.
  • the object to be cleaned is moved from the position of S2 to the position of S3 and immersed in the rinse liquid.
  • the time for immersing in the rinsing tank that is, the rinsing time corresponding to the contact time between the rinsing liquid and the object to be cleaned is not particularly limited, and is preferably 1 second to 60 minutes, more preferably 10 seconds to 30 minutes. preferable.
  • the cleaning agent composition and the stain component slightly adhered to the object to be cleaned are replaced with the rinsing liquid.
  • the step (3C) is a step of placing the object to be cleaned in the steam area generated from the steam tank and performing steam cleaning.
  • the object to be cleaned is moved from the position of S3 to the position of S4, which is the upper part of the steam tank. Then, steam cleaning is performed by bringing the object to be cleaned into contact with steam generated from the steam tank.
  • the steam cleaning conditions are as described above in step (1B).
  • the cleaning system 4 is a one-cycle type cleaning machine.
  • An ultrasonic cleaning tank containing a cleaning agent composition containing the component (A) and the component (B), the object to be cleaned is immersed, and the object to be cleaned is immersed and cleaned, and steam of the cleaning agent is generated.
  • the outline of the cleaning system 4 is shown in FIG.
  • the cleaning system 4 preferably includes an ultrasonic cleaning tank (12 in FIG. 4) containing a cleaning agent (1 in FIG. 4) and a steam tank (3 in FIG. 4) containing a cleaning agent (3 in FIG. 4).
  • the recovery section for example, 21 and 22 in FIG. 4) and the recovery section.
  • It is equipped with a water separator (23 in FIG. 4) that separates water from the collected liquid, extracts the cleaning agent, and supplies the extracted cleaning agent to the ultrasonic cleaning tank.
  • the cleaning system 4 corresponds to a cleaning system 1 further provided with an ultrasonic cleaning tank, except that the cleaning agent is returned from the water separator to the ultrasonic cleaning tank and the cleaning is performed in the ultrasonic cleaning tank.
  • the solid arrow indicates the flow of the cleaning agent.
  • the ultrasonic cleaning tank and steam tank in the cleaning system 4 are as described above in the cleaning systems 1 to 3.
  • the cleaning agent extracted by the water separator is supplied to the ultrasonic cleaning tank. Further, the liquid level of the ultrasonic cleaning tank is higher than the liquid level of the steam tank, so that the cleaning liquid overflows from the ultrasonic cleaning tank to the steam tank.
  • the cleaning method using the cleaning system 4 includes the following steps: (4A) a step of immersing the object to be cleaned in an ultrasonic cleaning tank for ultrasonic cleaning, and (4B) steam generated from the steam tank for the object to be cleaned. Includes a step of placing in an area and cleaning with steam.
  • the step (4A) is a step of immersing the object to be cleaned (S in FIG. 4) in an ultrasonic cleaning tank and performing ultrasonic cleaning.
  • the conditions in the step (4A) are as described above in the step (2A), including the preferable ones.
  • the step (4B) is a step of placing the object to be cleaned in the steam area generated from the steam tank and performing steam cleaning.
  • the object to be cleaned is moved from the position of S2 to the position of S4, which is the upper part of the ultrasonic cleaning tank, and placed in the steam area.
  • steam cleaning is performed by bringing the object to be cleaned into contact with steam generated from the steam tank.
  • the conditions in the step (4B) are as described above in the step (2B), including the preferable ones. After that, the object to be cleaned is moved to the position of S5 where the cleaning is completed, and the cleaning is completed.
  • a distillation regeneration device may be installed in each cleaning system.
  • the uncured resin is preferably a urethane resin and / or an epoxy resin.
  • the oil is preferably mineral oil, vegetable oil, wax and / or silicone oil.
  • the oily stain is preferably the above-mentioned preferable uncured resin, oil and / or flux stain.
  • the cleaning agent is a hand-wiping detergent, it is preferable that the oil is a mineral oil and the oily stain is a resin stain.
  • the cleaning agent does not contain a substance removed by the cleaning agent (that is, one or more selected from the group consisting of oily stains, oil, flux and uncured resin). Further, it is preferable that the cleaning agent does not contain a compound having a silicon atom and / or a silicone such as polydimethylsiloxane.
  • the total content of the component (B) is 25 parts by weight of (b2) ether, (b3) ester (excluding (b2) ether) and (b4) alcohol (excluding (b2) ether). It may be the above, or it may not contain the said component.
  • the component (B) is (b1), (b2), and.
  • One or a combination of two or more selected from the group consisting of the components (b3) and (b8) may be selected from the group consisting of nitromethane, propylene glycol monomethyl ether, dimethyl carbonate and 1-bromopropane. It may contain one kind or a combination of two or more kinds.
  • the preferable content of each component may be the following in addition to the content of the solvent composition described above.
  • the uncured resin is a urethane resin and / or an epoxy resin, and a cleaning agent for cleaning the object to be cleaned to which the stain is attached
  • the content of is preferably 3 parts by weight or more, more preferably 10 parts by weight or more and 90 parts by weight or less, further preferably 15 parts by weight or more and 80 parts by weight or less, and 30 parts by weight or more and 70 parts by weight or less. It is particularly preferable that the content is less than or equal to a portion.
  • the content of the component (A) is 10 parts by weight when the total amount of the solvent composition is 100 parts by weight.
  • the above is preferable, and the content of the component (A) and the component (B) when the total amount of the solvent composition is 100 parts by weight is particularly preferable in the cleaning agent of 50 parts by weight or more and 100 parts by weight or less.
  • the total is preferably 70 parts by weight or more and 100 parts by weight or less, more preferably 80 parts by weight or more and 100 parts by weight or less, and particularly preferably 90 parts by weight or more and 100 parts by weight or less.
  • the solvent composition is excellent in the solubility of the cured product of the resin, it can be used as a dissolving agent for the cured product of the resin. Therefore, the present invention also relates to the use of the solvent composition as a dissolving agent for the cured product of the resin.
  • the cured product of the resin includes a cured product composed of only the resin and a cured product of the resin composition containing the additive to be blended in the resin. Further, in the cured product of the resin, in addition to the cured product that is cured by accelerating the curing reaction of the resin, additives contained in the resin such as a reaction diluent volatilize and solidify as the viscosity increases. Things are also included.
  • the resin in the cured product of the resin is not particularly limited, and examples of the uncured resin include the above-mentioned resins.
  • a method for dissolving a cured resin product using a dissolving agent includes a step of bringing the dissolving agent into contact with the cured resin product. In the step of bringing the solubilizer into contact with the cured resin, the cured resin is dissolved in the lysing agent.
  • the contact time between the solubilizer and the cured product of the resin is not particularly limited as long as the desired effect can be achieved. The contact time is preferably 5 seconds to 24 hours, more preferably 10 seconds to 8 hours, and particularly preferably 10 minutes to 2 hours. Within the above time range, the cured product of the resin can be sufficiently dissolved.
  • all of the cured resin may be dissolved to form a uniform phase with the solubilizer, and all or part of the cured resin may be swelled by the lysing agent, and the lysing agent may be used.
  • the swelling product of the resin may be present as two layers, and the cured product of the resin may be fragmented by dissolving a part of the cured product of the resin. It is preferable that the entire cured product of the resin is dissolved to form a uniform phase with the dissolving agent. Further, when the amount of the cured product of the resin to be dissolved exceeds the saturated dissolution amount of the dissolving agent, a part of the cured product of the resin may remain undissolved.
  • the temperature of the dissolving agent when the dissolving agent and the cured product of the resin are brought into contact with each other is not particularly limited, but may be 0 ° C to 100 ° C, 0 ° C to 50 ° C, or 5 ° C to 5 ° C. It may be 40 ° C. Further, the temperature of the dissolving agent may be 20 ° C to 80 ° C.
  • the present invention also relates to the use of the solvent composition in which the cured product of the resin is dissolved as a coating agent for the resin.
  • the resin coating agent is a composition in which a cured product of the resin is dissolved in a dissolving agent. Therefore, the resin coating agent can be produced by a method including a step of dissolving a cured product of the resin in the solvent composition.
  • a coating film of a cured resin is formed.
  • a resin molded product having a desired shape can be obtained. In the coating agent, a part of the cured resin may be undissolved.
  • the content of the cured resin in the coating agent is preferably not more than the saturated dissolution amount of the cured resin. With such a content, there is no cured product of undissolved resin, and a homogeneous coating and / or resin molded product can be obtained.
  • the solvent composition is excellent in the solubility of the cured product of the resin, it can be used as an adhesive for the cured product of the resin. Therefore, the present invention also relates to the use of the solvent composition as an adhesive for the cured resin.
  • the adhesive means a solvent adhesive that melts and adheres a cured resin. That is, the adhesive exhibits the adhesive function by bringing the base material, which is a cured product of the resin, into contact with the dissolving agent, dissolving a part of the adhesive surface of the base material, and volatilizing the solvent agent. Based on.
  • the adhesive surface can be firmly adhered without inclusions such as a reaction-curing adhesive (for example, cyanoacrylate in a cyanoacrylate adhesive).
  • the method for producing an adhesive using an adhesive includes a step of bringing the adhesive into contact with a dissolving agent.
  • the method for producing an adhesive is (A1) a step of applying the dissolving agent to the adhered surface of one base material to dissolve a part of the adhered surface of one base material, and (B1) Includes a step of laminating the other base material and laminating the base materials to each other via the adhered surface of the one base material in which a part of the base material has been dissolved.
  • the method for producing an adhesive is (A1) a step of applying the dissolving agent to the adhered surface of one base material to dissolve a part of the adhered surface of one base material, (B2). A step of applying the dissolving agent to the adhered surface of one substrate to dissolve a part of the adhered surface of the other substrate, and (C2) one substrate and the other substrate.
  • the present invention includes a step of adhering the base materials to each other via the adhered surface of one of the base materials in which the part is dissolved and the adhered surface of the other base material in which the part is dissolved.
  • the method for producing an adhesive may include the above steps (A1) and (B1), and the steps of repeating the above steps (A1), (B2) and (C2) to further bond the substrate. ..
  • the method of applying the dissolving agent is not particularly limited, and examples thereof include application, spraying, and spray gun.
  • the time for bonding the substrates to each other is not particularly limited as long as the desired effect can be achieved.
  • the contact time is preferably 1 minute to 10 hours, and particularly preferably 30 minutes to 2 hours. Within the above time range, the adhesive force between the base materials is sufficiently exhibited.
  • a step of heating at a temperature of 50 to 80 ° C. may be included in some cases. This promotes curing and increases the adhesive strength.
  • Acrylic resin, polycarbonate resin, acrylonitrile, butadiene, styrene resin, silicone resin, urethane can be used as the curing agent of the cured resin, the adhesive of the cured resin, and the cured resin dissolved in the resin coating agent. It is preferably one or more selected from a resin, a polyamide resin and a polyacetal resin.
  • the component (B) is selected from the group consisting of the components (b1), (b3), (b6), (b7), (b8), (b10), (b11), (b12) and (b13) 1 It may be a species or a combination of two or more species, or it may be a combination of one species or two species.
  • the solvent composition is used as a dissolving agent for a cured resin, an adhesive for a cured resin, and a coating agent for a resin
  • the preferable content of each component is in addition to the content of the solvent composition described above. It may be as follows.
  • the content of the component (A) may be 50 parts by weight or more. Further, when the component (B) is a combination of the component (b6) and the component (b10), the content of the component (A) may be 50 parts by weight or more.
  • compositions of Examples and Comparative Examples were prepared by using the following solvents as they were or by mixing each solvent according to the composition (part by weight) in the table.
  • Oils, etc. Mineral oil: Daphne Marg Plus ST25 (manufactured by Idemitsu Kosan Co., Ltd.) (hydrogenated low-viscosity paraffin 90% by weight or more and 100% by weight or less, sulfide oil and fat 1% by weight or more and less than 10% by weight, hydrided medium-viscosity paraffin 1% by weight or more and less than 10% by weight, 2,6-di-terriary butyl-4-cresol 0.1% by weight or more and less than 1% by weight, solvent-dewaxed heavy paraffin-based oil distillate 0.1% by weight or more and 1% by weight Less than%, lubricating oil additive less than 2% by weight)
  • Vegetable oil Edible olive oil (AJINOMOTO Olive Oil Extra Virgin, manufactured by J-Oil Mills Co., Ltd.)
  • Silicone oil Dimethyl silicone oil 350CS (Shin-Etsu Chemical Co., Ltd., KF96-350CS-1, viscosity 350c
  • Cured resin (1) Cured acrylic resin: Acrylic plate (manufactured by Acrylic Sunday Co., Ltd .; Acrylic Sunday EX plate; Color number / EX001 Thickness 2 mm) (2) Cured product of polycarbonate resin (PC resin): Polycarbonate resin plate (manufactured by Hikari Co., Ltd., 30 mm x 10 mm x 2 mm) (3) Cured product of acrylonitrile-butadiene-styrene resin (ABS resin): ABS type resin plate (manufactured by Takachi Denki Kogyo Co., Ltd., 300 mm x 200 mm x 1.0 mm) (4) Epoxy resin cured product: Epoxy adhesive cured product (Huntsman Japan Co., Ltd., Araldite (registered trademark) Standard, a mixture of the main agent and the curing agent in a weight ratio of 1: 1) (5) Cured product of cyanoacrylate resin: Cured product of cyanoacrylate adhesive (ThreeBond
  • Test Example 2 Degreasing performance confirmation test An oil dissolution test and an oil cleaning test were conducted on mineral oil, silicone oil, and vegetable oil to evaluate the degreasing performance.
  • Oil dissolution test 0.15 g of oil was placed in a test tube (capacity: 4 ml, 10 ⁇ 75 mm, manufactured by PYREX®). Subsequently, 3 g of the solvent composition at room temperature (about 20 ° C.) was placed in a test tube. The oil solubility was evaluated by observing the state of the oil when it was stirred 10 times using a Pasteur pipette.
  • the cleaning test sample was immersed in the solvent composition under the conditions. After 3 minutes, the test sample was taken out from the beaker and immersed in 50 mL of a solvent composition for rinsing having the same composition as the solvent composition having a liquid temperature of about 40 ° C. prepared in advance in another 100 mL beaker under ultrasonic wave generation. After 1 minute, it was pulled out of the liquid and naturally dried, and then the surface of the test sample was observed with the naked eye or using an HD ⁇ I digital stereomicroscope STZ-161-TLED1080 ⁇ (manufactured by Shimadzu Rika Co., Ltd.). (criterion) ⁇ : Uniform transparency was observed in the oil dissolution test, and no oil stain was observed in the oil cleaning test.
  • Test Example 3 Hand towel test 0.1 g of mineral oil was dropped on the surface of a SUS304 plate (manufactured by Iwata Seisakusho Co., Ltd., 100 mm ⁇ 100 mm ⁇ 0.1 mm), or a straight line was drawn with a McKee pen to prepare a cleaning test sample.
  • a set of two layers of tissue paper (manufactured by Oji Nepia Co., Ltd.) with a size of 65 mm in length and 72 mm in width is folded in four and soaked with the solvent composition of each example, and the thumb and index finger are used. I squeezed it once.
  • the tissue paper impregnated with each solvent composition was brought into contact with the surface of the SUS304 plate and wiped by rubbing by hand.
  • Test Example 4 Flux cleaning test (1)
  • a lead-free solder paste for SMT surface mount was applied to a zinc-drawn iron plate (equivalent to JIS G3302, length 30 mm, width 30 mm, thickness 0.3 mm) via a metal mask. It was placed on a hot plate at about 180 ° C. for 3 minutes, followed by a hot plate at about 250 ° C. for 5 minutes. Further, the mixture was cooled to room temperature (about 20 ° C.) and left to stand for 2 days to obtain a cleaning test sample (object to be cleaned with rosin-containing cream solder stains).
  • Test Example 5 Aerosol cleaning test 0.1 g of mineral oil was dropped into a 100 mm ⁇ 100 mm section on a SUS430 flat plate (manufactured by Hikari Co., Ltd., 400 mm ⁇ 300 mm ⁇ 1 mm), and uniform using a round brush No. 3 (horsehair). Was applied to. 300 ml of each solvent composition was placed in an aluminum refillable air spray can A1631D (capacity 650 ml, manufactured by FIRSTINFO TOOLS CO., LTD.), And then filled with nitrogen gas (0.6 MPa). (Test method) The aerosol composition was sprayed for 10 seconds from 50 cm from the test sample. (Test results) ⁇ : The oil could be removed with the naked eye from the section to which the oil was applied. X: Residual oil was observed with the naked eye in the section to which the oil was applied.
  • Test Example 6 Acrylic resin dissolution test An acrylic plate was cut into 5 mm ⁇ 10 mm to obtain an acrylic test piece. After putting 4 g of the solubilizer of each example shown in the table into the test tube, the cut acrylic test piece was immersed. After being left at room temperature (18 to 22 ° C.), the dissolving power of the cured product of the acrylic resin was evaluated by the following. ⁇ : All the cured resin was dissolved within 2 hours. ⁇ : All the cured resin was dissolved within more than 2 hours and 8 hours. ⁇ : All the cured resin was dissolved within more than 8 hours and 24 hours. X: The cured resin did not dissolve within 24 hours.
  • the dissolving agent in which the acrylic test piece was dissolved had a uniform liquid phase. Further, when the solvent was volatilized, the acrylic resin was cured again, and the shape of the acrylic resin could be freely changed. Further, the color of the acrylic resin cured again maintained the color of the melted acrylic resin piece and was transparent. Therefore, the dissolving agent in which the acrylic test piece (cured product of acrylic resin) was dissolved could also be used as a coating agent.
  • Test Example 7 Adhesion test (1) Adhesion test of acrylic resin Two acrylic plates (cut into a length of 10 ⁇ width of 30 ⁇ thickness of 2 mm) were used. A drop of each composition was dropped in the center of one acrylic plate using a Pastool pipette. Next, the other acrylic plate was attached to the surface to which the dissolving agent of one acrylic plate was applied so as to form a cross. The spilling solubilizer was wiped off with tissue paper. After leaving for 1 hour, an adhesive was obtained. The adhesiveness of the adhered body was evaluated by the following method. (Adhesion test) ⁇ : Adhesion is possible, and even if you try to peel it off manually, it cannot be peeled off.
  • Adhesion is possible and it will not come off even if it is dropped from a place with a height of 1 m three times, but it can be peeled off if it is forcibly peeled off by human power.
  • Adhesion is possible, but if dropped from a place with a height of 1 m, it will peel off within 3 times.
  • Cannot adhere at all
  • Test Example 8 Flux cleaning test (2) (1) Preparation of cleaning test sample A lead-free solder paste for SMT (surface mount) was applied to a zinc-drawn iron plate (equivalent to JIS G3302, length 30 mm, width 30 mm, thickness 0.3 mm) via a metal mask. It was placed on a hot plate at about 180 ° C. for 3 minutes, followed by a hot plate at about 250 ° C. for 60 minutes. Further, the mixture was cooled to room temperature (about 20 ° C.) and left to stand for 7 days to obtain a cleaning test sample (a substance to be cleaned to which stains of cream solder containing rosin were attached). This cleaning test sample is a sample in which the flux component adheres more firmly and is difficult to clean than the sample in Test Example 4: Flux cleaning test (1).
  • Test Example 9 Paraffin wax cleaning test (1) Preparation of cleaning test sample Paraffin wax was heated at 100 ° C to make it liquid. A SUS304 plate (manufactured by Iwata Seisakusho Co., Ltd., 10 mm ⁇ 10 mm ⁇ 0.1 mm) was immersed therein, and after 10 seconds, it was pulled up and left at room temperature to obtain a cleaning test sample to which paraffin wax was adhered. (2) Cleaning test An ultrasonic cleaner US-13KS (oscillation frequency: 38 kHz, high frequency output: 360 W) manufactured by SND Co., Ltd. was filled with tap water and the water temperature was adjusted to about 40 ° C.
  • US-13KS oscillation frequency: 38 kHz, high frequency output: 360 W
  • the device used in this test method corresponds to the cleaning system 4 described above.
  • The surface was clean.
  • A very small amount of residue was observed, but the level did not adversely affect actual use.
  • X A clear residue was observed, which was at a level that adversely affected actual use.
  • VOC test This is a VOC test specified in the Chinese regulation GB38508-2020 (limit value of volatile organic compound (VOC) content in detergent). 2 g of each composition was weighed in a 50 mm ⁇ 30 mm weighing bottle (manufactured by AGC Technoglass Co., Ltd.) and allowed to stand in a constant temperature bath set at 105 ° C. for 4 hours. Then, it was cooled in a desiccator for 30 minutes and weighed. The VOC content percent (Wv) in the test sample was calculated by dividing the reduction by the original weight (2 g). The VOC content (X) in the test sample was calculated by the following formula.
  • HFC-43-10mee, HFO-1336mzz (Z), HFE-7200, etc. are also applicable.
  • Y Density of test sample (g / L) (criterion)
  • X is 900 (g / L) or less.
  • X X is over 900.
  • Test Example 11 Adhesive dissolution test 0.1 g of each adhesive was applied on a SUS304 plate (manufactured by Iwata Seisakusho Co., Ltd., 35 mm x 15 mm x 0.1 mm) and allowed to stand at room temperature (about 20 ° C) for one week. , A sample to which a cured product of each resin was attached was obtained. 80 mL of each solvent composition was placed in a 100 mL beaker, sealed with aluminum foil, and heated on a hot plate to a liquid temperature of about 60 ° C. It was evaluated according to the following criteria.
  • Test Example 12 Resin cured product dissolution test In a test tube (capacity: 4 ml, 10 ⁇ 75 mm, manufactured by PYREX®) covered with aluminum foil, the amounts of each resin described below are added to 2 g of each composition. It was immersed and allowed to stand at room temperature (about 20 ° C.), and evaluated according to the following criteria.
  • the solvent composition contains p-chlorobenzotrifluoride, it is a solvent composition having a low environmental load. Further, from Test Examples 1 to 9 and 11 to 12, the solvent composition has excellent solubility of resins and the like, and is a cleaning agent, an aerosol composition, a dissolving agent for a cured resin, a coating agent for a resin, and a cured product for a resin. It had an excellent effect as an adhesive for. Further, from Test Example 10, the solvent composition was a solvent composition having a reduced VOC and a low environmental load. From Test Example 1, when the content of the component (B) was 30 parts by weight or more with respect to a total of 100 parts by weight of the solvent composition, the solubility of the uncured resin was excellent.
  • the solubility of the uncured resin was superior.
  • the content of propylene glycol monomethyl ether is 5 with respect to a total of 100 parts by weight of the solvent composition. Even when the amount was up to 20 parts by weight, the solubility of the uncured resin was superior when combined with 1-bromopropane or trans-1,2-dichloroethylene.
  • the group further comprises a nitro compound, a cyclic ether and an epoxide.
  • Example 337 in Test Example 6 the solubility of the cured product of the resin was superior in the same case.
  • the component (B) contains 1-bromopropane in a specific amount.
  • Examples 183 to 198 when a specific amount of 1-bromopropane and propylene glycol monomethyl ether is contained (Examples 199 to 222), and when a specific amount of trans-1,2-dichloroethylene and propylene glycol monomethyl ether is contained. (Examples 230 to 235) were excellent in the detergency of the flux.

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  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Detergent Compositions (AREA)

Abstract

La présente invention concerne une composition de solvant qui a une excellente aptitude à dissoudre une résine, ou similaire, et qui cause moins de charge environnementale. La composition de solvant contient (A) du p-chlorobenzotrifluorure, et, éventuellement, contient en outre (B) un ingrédient supplémentaire qui est une ou plusieurs espèces choisies dans le groupe constitué par (b1) un composé nitro, (b2) un éther, (b3) un ester (à l'exclusion de (b2) l'éther), (b4) un alcool (à l'exclusion de (b2) l'éther), (b5) un composé amide, (b6) une chloro-oléfine, (b7) une hydrofluoro-oléfine, (b8) un hydrobromocarbure, (b9) un hydrofluorocarbure (b10) un hydrofluoroéther, (b11) un hydrocarbure, (b12) un hydrocarbure chloré (à l'exclusion de (b6) la chloro-oléfine, (b7) l'hydrofluoro-oléfine et (b11) l'hydrocarbure) et (b13) une combinaison d'acide sulfurique et d'une ou plusieurs espèces choisies dans le groupe constitué d'un acide sulfonique d'alkylbenzène et d'un sel de celui-ci. La présente invention concerne également un dispositif de nettoyage, une composition d'aérosol de nettoyage, un solvant pour un produit durci de résine, un adhésif pour un produit durci de résine, et un agent de revêtement de résine, qui utilisent la composition de solvant.
PCT/JP2021/003350 2020-09-03 2021-01-29 Composition de solvant et son application WO2022049797A1 (fr)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2024129533A1 (fr) * 2022-12-14 2024-06-20 The Lubrizol Corporation Compositions pour préparer des membranes à partir de solutions polymères

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07505416A (ja) * 1992-03-25 1995-06-15 オクシデンタル ケミカル コーポレイション エポキシ製品を洗浄する方法
JP2010526918A (ja) * 2007-05-11 2010-08-05 エクスプローラー プレスルーム ソリューションズ 印刷機洗浄組成物
JP2018516309A (ja) * 2015-05-29 2018-06-21 ティービーエフ エンヴァイロンメンタル テクノロジー インコーポレイテッド ヘプタン代替品として使用するための溶剤組成物

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07505416A (ja) * 1992-03-25 1995-06-15 オクシデンタル ケミカル コーポレイション エポキシ製品を洗浄する方法
JP2010526918A (ja) * 2007-05-11 2010-08-05 エクスプローラー プレスルーム ソリューションズ 印刷機洗浄組成物
JP2018516309A (ja) * 2015-05-29 2018-06-21 ティービーエフ エンヴァイロンメンタル テクノロジー インコーポレイテッド ヘプタン代替品として使用するための溶剤組成物

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2024129533A1 (fr) * 2022-12-14 2024-06-20 The Lubrizol Corporation Compositions pour préparer des membranes à partir de solutions polymères

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