Wood preservative treatment solution, and method for manufacturing wood with wood preservative agent

Abstract

Provided is a wood-preserving treatment solution comprising: an organic solvent that includes 1-chloro-2,3,3,3-tetrafluoropropene; and a wood preservative.

Description

[Technical Field]

[0001] The present disclosure relates to a wood preservative treatment solution and a method for producing wood with a wood preservative. [Background technology]

[0002] Wood is a material used in a variety of fields, but it has the drawback of being subject to decay and deterioration due to fungal corrosion and insect attack, resulting in a loss of strength. Therefore, various wood preservative treatment solutions have been developed to prevent deterioration by fungi and insects, and methods for manufacturing wood preservative-treated wood using these solutions have been developed.

[0003] Japanese Patent Application Laid-Open No. 2021-66174 discloses a chemical treatment agent composition containing an active ingredient that modifies wood materials and an organic solvent containing hydrofluoroolefins that dissolves the active ingredient. Summary of the Invention [Problem to be solved by the invention]

[0004] One of the properties required for a wood preservative treatment solution is its ability to penetrate into wood. If a wood preservative treatment solution has high penetration into wood, it can increase the amount of wood preservative introduced into the wood, thereby further suppressing wood deterioration. The present inventors have investigated the penetration into wood using hydrofluoroolefins (e.g., 1-chloro-3,3,3-trifluoro-1-propene) specifically disclosed in JP 2021-66174 A and found that further improvement is necessary.

[0005] In view of the above circumstances, an object of the present disclosure is to provide a wood preservative treatment solution that has excellent permeability into wood. Another object of the present disclosure is to provide a method for producing wood coated with a wood preservative. [Means for solving the problem]

[0006] The present inventors have found that the above problems can be solved by the following configuration.

[0007] (1) A wood preservative treatment solution comprising an organic solvent containing 1-chloro-2,3,3,3-tetrafluoropropene and a wood preservative agent. (2) The wood preservative treatment solution according to (1), wherein the content of 1-chloro-2,3,3,3-tetrafluoropropene is 50% by mass or more based on the total mass of the organic solvent. (3) The wood preservative treatment solution according to (1) or (2), wherein the content of the organic solvent is 70 to 99.998 mass % based on the total mass of the wood preservative treatment solution. (4) 1-chloro-2,3,3,3-tetrafluoropropene includes the Z isomer of 1-chloro-2,3,3,3-tetrafluoropropene and the E isomer of 1-chloro-2,3,3,3-tetrafluoropropene, The wood preservative treatment solution according to any one of (1) to (3), wherein the content of the Z isomer of 1-chloro-2,3,3,3-tetrafluoropropene is 50% by mass or more based on the total amount of the Z isomer of 1-chloro-2,3,3,3-tetrafluoropropene and the E isomer of 1-chloro-2,3,3,3-tetrafluoropropene. (5) The wood preservative treatment solution according to any one of (1) to (4), wherein the wood preservative is at least one selected from ammonium-based wood preservatives, triazole-based wood preservatives, neonicotinoid-based wood preservatives, phenylpyrazole-based wood preservatives, phenylpyrrole-based wood preservatives, benzoylphenylurea-based wood preservatives, anthranilic diamide-based wood preservatives, strobilurin-based wood preservatives, pyrethroid-based wood preservatives, and copper or zinc salts of fatty acids and fatty acids having an aromatic ring. (6) A wood preservative treatment solution according to any one of (1) to (4), wherein the wood preservative is at least one selected from triazole wood preservatives, neonicotinoid wood preservatives, pyrethroid wood preservatives, and copper or zinc salts of fatty acids and fatty acids having an aromatic ring. (7) The wood preservative treatment solution according to any one of (1) to (4), wherein the wood preservative is at least one selected from (2RS,3RS;2RS,3SR)-2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol, 1-[(6-chloro-3-pyridinyl)methyl]-4,5-dihydro-N-nitro-1H-imidazol-2-amine, 2-(4-ethoxyphenyl)-2-methylpropyl-3-phenoxybenzyl ether, zinc naphthenate, and copper naphthenate. (8) The wood preservative treatment solution according to any one of (1) to (7), wherein the content of the wood preservative agent is 0.002 to 30% by mass based on the total mass of the wood preservative treatment solution. (9) The wood preservative treatment solution according to any one of (1) to (8), which is substantially free of water or contains 10% by mass or less of water based on the total mass of the wood preservative treatment solution. (10) A wood preservative treatment solution according to any one of (1) to (9), in which, when the ratio of the mass of wood after treatment to the mass of wood before treatment is measured based on the permeability test described below, the ratio is 3.0 or more both when the pressure inside the pressure-resistant container is 0.05 MPaG and when it is 0.10 MPaG. (Permeability test) A piece of cedar wood measuring 15mm thick x 15mm wide x 50mm long is placed in a glass tube, and an amount of wood preservative treatment solution is poured into the glass tube so that the entire piece of wood is immersed.The glass tube is then placed in a pressure-resistant container and sealed, and the pressure inside the pressure-resistant container is pressurized using compressed air to 0.05MPaG or 0.10MPaG.The container is then left to stand for 30 minutes in a 25°C environment, and the piece of wood is then removed from the container.The ratio of the post-treatment wood mass, which is the mass of the piece of wood immediately after removal, to the pre-treatment wood mass, which is the mass of the piece of wood before the permeability test, is calculated for both cases where the pressure inside the pressure-resistant container is 0.05MPaG and 0.10MPaG. (11) A method for producing wood preservative-treated wood, comprising contacting wood with the wood preservative treatment solution according to any one of (1) to (10) and volatilizing the organic solvent to produce wood preservative-treated wood. [Effects of the Invention]

[0008] According to one embodiment of the present disclosure, a wood preservative treatment solution that has excellent permeability into wood can be provided. Furthermore, according to one embodiment of the present disclosure, a method for producing wood coated with a wood preservative can be provided. DETAILED DESCRIPTION OF THE INVENTION

[0009] An embodiment of the present disclosure will be described in detail below. In this specification, a numerical range expressed using "to" means a range that includes the numerical values ​​before and after "to" as the lower and upper limits. In this specification, the abbreviation of a compound is written in parentheses after the compound name, and if necessary, this abbreviation is used instead of the compound name. Furthermore, for compounds having geometric isomers, the (E) attached to the name and abbreviation indicates the E form (trans form), and the (Z) attached to the abbreviation indicates the Z form (cis form). When the name or abbreviation of the compound does not specify the E form or the Z form, the name or abbreviation is a generic term that includes the E form, the Z form, and a mixture of the E form and the Z form.

[0010] A characteristic feature of the wood preservative treatment solution of the present disclosure is that it uses 1-chloro-2,3,3,3-tetrafluoropropene (CF3-CF=CHCl, HCFO-1224yd; hereinafter, simply referred to as 1224yd). Studies by the present inventors have revealed that 1224yd has high permeability into wood, and that the wood preservative treatment solution of the present disclosure has high permeability into wood.

[0011] The wood preservative treatment solution of the present disclosure comprises an organic solvent containing 1224 yd and a wood preservative agent. Each component will be described in detail below.

[0012] (organic solvent) The organic solvent comprises 1224 yd. 1224yd may be the Z-isomer (cis-isomer) of 1224yd or the E-isomer (trans-isomer) of 1224yd. The wood preservative treatment solution of the present disclosure may contain only the Z-isomer of 1224yd, only the E-isomer of 1224yd, or both the Z-isomer and the E-isomer of 1224yd. Among these, the organic solvent preferably contains at least the Z-isomer of 1224yd because of its higher volatility.

[0013] The content of the Z isomer of 1224yd relative to the total amount of the Z isomer of 1224yd and the E isomer of 1224yd is preferably 50% by mass or more, more preferably 70% by mass or more, in order to maintain superior volatility of the Z isomer, and the upper limit may be 100% by mass or less.

[0014] The content of 1224yd in the organic solvent is preferably 50% by mass or more, more preferably 70% by mass or more, and even more preferably 90% by mass or more, based on the total mass of the organic solvent. The upper limit of the content of 1224yd in the organic solvent is 100% by mass or less.

[0015] As long as the organic solvent contains 1224 yd, it may or may not contain other solvents. The organic solvent is preferably one that can disperse or dissolve the wood preservative. When the organic solvent contains other organic solvents than 1224 yd, the content of the other organic solvents is preferably less than 50 mass %, more preferably 30 mass % or less, and even more preferably 10 mass % or less, based on the total mass of the organic solvents. The lower limit of the content of other organic solvents than 1224 yd in the organic solvent is 0 mass %. The other organic solvents may be used singly or in combination of two or more.

[0016] Other organic solvents include hydrocarbons, alcohols, ketones, ethers (excluding hydrofluoroethers), esters, nitrogen-containing organic solvents, and halogenated hydrocarbons (excluding 1224yd).

[0017] The hydrocarbons are preferably linear or cyclic saturated or unsaturated hydrocarbons having 5 to 8 carbon atoms, and specific examples thereof include n-pentane, 2-methylbutane, n-hexane, 2-methylpentane, 2,2-dimethylbutane, 2,3-dimethylbutane, n-heptane, 2-methylhexane, 3-methylhexane, 2,4-dimethylpentane, n-octane, 2-methylheptane, 3-methylheptane, 4-methylheptane, 2,2-dimethylhexane, 2,5-dimethylhexane, 3,3-dimethylhexane, 2-methyl-3-ethylpentane, 3-methyl-3-ethylpentane, 2,3,3-trimethylpentane, 2,3,4-trimethylpentane, 2,2,3-trimethylpentane, 2-methylheptane, 2,2,4-trimethylpentane, cyclopentane, methylcyclopentane, cyclohexane, methylcyclohexane, ethylcyclohexane, and cyclohexene. Of these, n-pentane, cyclopentane, n-hexane, cyclohexane, and n-heptane are more preferred. The hydrocarbons may be hydrocarbons having 9 or more carbon atoms, such as mineral oil, kerosene, petroleum benzine, etc. The hydrocarbons may also be aromatic hydrocarbons, such as toluene and xylene.

[0018] The alcohols are preferably linear or cyclic saturated or unsaturated alcohols having 1 to 6 carbon atoms, specifically methanol, ethanol, n-propyl alcohol, isopropyl alcohol, n-butyl alcohol, sec-butyl alcohol, isobutyl alcohol, tert-butyl alcohol, 1-pentanol, 2-pentanol, 1-ethyl-1-propanol, 2-methyl-1-butanol, 3-methyl-1-butanol, 3-methyl-2-butanol, neopentyl alcohol, 1-hexanol, 2-methyl-1-pentanol, 4-methyl-2-pentanol, 2-ethyl-1-butanol, allyl alcohol, propargyl alcohol, benzyl alcohol, and cyclohexanol. Among these, methanol, ethanol, and isopropyl alcohol are more preferred.

[0019] As the ketones, linear or cyclic saturated or unsaturated ketones having 3 to 6 carbon atoms are preferred, and specific examples thereof include acetone, methyl ethyl ketone, 2-pentanone, 3-pentanone, 2-hexanone, methyl isobutyl ketone, and cyclohexanone. Of these, acetone and methyl ethyl ketone are more preferred.

[0020] The ethers are preferably linear or cyclic saturated or unsaturated ethers having 2 to 6 carbon atoms, and specific examples thereof include diethyl ether, dipropyl ether, diisopropyl ether, dimethoxymethane, ethyl vinyl ether, butyl vinyl ether, dioxane, furan, methylfuran, and tetrahydrofuran. Of these, diethyl ether, diisopropyl ether, dimethoxymethane, dioxane, and tetrahydrofuran are more preferred.

[0021] The esters are preferably linear or cyclic saturated or unsaturated esters having 2 to 8 carbon atoms, specifically methyl formate, ethyl formate, propyl formate, butyl formate, isobutyl formate, pentyl formate, methyl acetate, ethyl acetate, propyl acetate, isopropyl acetate, butyl acetate, isobutyl acetate, sec-butyl acetate, pentyl acetate, methoxybutyl acetate, sec-hexyl acetate, 2-ethylbutyl acetate, cyclohexyl acetate, benzyl acetate, methyl propionate, ethyl propionate, butyl propionate, methyl butyrate, ethyl butyrate, butyl butyrate, isobutyl isobutyrate, ethyl 2-hydroxy-2-methylpropionate, methyl benzoate, ethyl benzoate, γ-butyrolactone, diethyl oxalate, diethyl malonate, dimethyl maleate, diethyl maleate, and dimethyl tartrate. Of these, methyl acetate and ethyl acetate are more preferred.

[0022] Specific examples of the nitrogen-containing organic solvent include N-methyl-2-pyrrolidone, N-methylpyrrole, dimethylformamide, dimethylsulfoxide, pyrrole, N-methylpyrrole, N-methylmorpholine, pyridine, and N-methylpyridine. Halogenated hydrocarbons (excluding 1224yd) include methylene chloride, trichloroethylene, tetrachloroethylene, 1,2-dichloroethylene (either cis or trans isomers, or both), 1-chloro-2,3,3-trifluoro-1-propene (either E or Z isomers, or both), 1-chloro-3,3,3-trifluoro-1-propene (either E or Z isomers, or both), 1,1,1,4,4,4-hexafluoro-2-butene (either cis or trans isomers, or both), 1,1,2,2-tetrafluoroethyl-2,2, Examples include 2-trifluoroethoxyethane, 1,1,1,2,2,3,3,4,4-nonafluoro-methoxybutane and 2-trifluoromethyl-1,1,1,2,3,3-nonafluoro-methoxypropane, 1,1,1,2,2,3,3,4,4-nonafluoro-ethoxybutane, 2-trifluoromethyl-1,1,1,2,3,3-nonafluoro-ethoxypropane, 1,1,1-2,3,4,4,5,5,5-decafluoro-3-methoxy-2-(trifluoromethyl)pentane, and isomers of perfluoroheptene ether.

[0023] The content of the organic solvent is preferably 70 to 99.998 mass %, more preferably 80 to 99.99 mass %, based on the total mass of the wood preservative treatment solution.

[0024] (Wood preservatives) The wood preservative agent may be any conventionally used wood preservative agent, and may be one used as a fungicide / insecticide, preservative, anti-termite agent, or anti-fungal agent to eliminate wood-destroying fungi and wood-eating insects such as termites. The wood preservative is mixed with an organic solvent containing the above 1224 yd and injected into the wood, and then the organic solvent is evaporated, leaving the chemical in the wood.

[0025] 1224yd exhibits excellent solubility in the wood preservatives mentioned above due to the presence of halogen atoms, particularly chlorine atoms, in the molecule. 1224yd is also thought to have polarity in the molecule due to the presence of unsaturated bonds (carbon-carbon double bonds). Therefore, among wood preservatives, ammonium-based wood preservatives, triazole-based wood preservatives, neonicotinoid-based wood preservatives, phenylpyrazole-based wood preservatives, phenylpyrrole-based wood preservatives, benzoylphenylurea-based wood preservatives, anthranilic diamide-based wood preservatives, strobilurin-based wood preservatives, pyrethroid-based wood preservatives, and copper or zinc salts of fatty acids and fatty acids with aromatic rings are thought to have particularly excellent solubility in 1224 yd.

[0026] Specific examples of ammonium-based wood preservatives include didecyldimethylammonium chloride, N,N-didecyl-N-methyl-polyoxyethyl-ammonium propionate, and N-alkylbenzyldimethylammonium chloride.

[0027] Specific examples of triazole-based wood preservatives include (2RS,3RS;2RS,3SR)-2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol, (RS)-1-p-chlorophenyl-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol, and 1-[[2-(2,4-dichlorophenyl)-4-propyl-1,3-dioxolan-2-yl]methyl]-1H-1,2,4-triazole.

[0028] Specific examples of neonicotinoid wood preservatives include (E)-N1-[(6-chloro-3-pyridyl)methyl]-N2-cyano-N1-methylacetamidine, 1-[(6-chloro-3-pyridinyl)methyl]-4,5-dihydro-N-nitro-1H-imidazol-2-amine, (E)-1-(2-chloro-1,3-thiazol-5-ylmethyl)-3-methyl-2-nitroguanidine, and (EZ)-3-(2-chloro-1,3-thiazol-5-ylmethyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene(nitro)amine.

[0029] A specific example of a phenylpyrazole-based wood preservative is 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)sulfonyl]-1H-pyrazole-3-carbonitrile.

[0030] A specific example of a phenylpyrrole wood preservative is 4-(2,2-difluoro-1,3-benzodioxol-4-yl)pyrrole-3-carbonitrile.

[0031] Specific examples of benzoylphenylurea-based wood preservatives include 1-[3,5-dichloro-4-(3-chloro-5-trifluoromethyl-2-pyridyloxy)phenyl]-3-(2,6-difluorobenzoyl)urea and (RS)-1-[3-chloro-4-(1,1,2-trifluoro-2-trifluoromethoxyethoxy)phenyl]-3-(2,6-difluorobenzoyl)urea.

[0032] A specific example of an anthranilic diamide wood preservative is 3-bromo-N-[4-chloro-2-methyl-6-(methylcarbamoyl)phenyl]-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxamide.

[0033] A specific example of a strobilurin wood preservative is methyl {2-[1-(4-chlorophenyl)pyrazol-3-yloxymethyl]phenyl}(methoxy)carbamate.

[0034] Specific examples of pyrethroid wood preservatives include (±)-α-cyano-3-phenoxybenzyl (+)-cis, trans-chrysanthemate, 2-(4-ethoxyphenyl)-2-methylpropyl-3-phenoxybenzyl ether, 4-ethoxyphenyl[3-(4-fluoro-3-phenoxyphenyl)propyl]dimethylsilane, and 2-methylbiphenyl-3-ylmethyl(Z)-(1RS,3RS)-3-(2-chloro-3,3,3-trifluoroprop-1-enyl)-2,2-dimethylcyclopropanecarboxylate. ester, (Z)-(S)-2-methyl-4-oxo-3-(penta-2,4-dienyl)cyclopent-2-enyl (1R)-trans-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylate, (Z)-(S)-2-methyl-4-oxo-3-(penta-2,4-dienyl)cyclopent-2-enyl (+)-trans-chrysanthemate, and 3-phenoxybenzyl 2-(2,2-dichlorovinyl)-3,3-dimethyl-1-cyclopropanecarboxylate.

[0035] Specific examples of copper or zinc salts of fatty acids and fatty acids having an aromatic ring include zinc naphthenate, copper naphthenate, zinc tertiary carboxylate, and zinc versatate. Other agents include zinc oxide, cupric oxide, copper (II) oxide, copper (II) oxide, copper (II) hydroxide, 4-bromo-2-(4-chlorophenyl)-1-ethoxymethyl-5-(trifluoromethyl)pyrrole-3-carbonitrile, (EZ)-2'-[2-(4-cyanophenyl)-1-(α,α,α-trifluoro-m-tolyl)ethylidene]-4-(trifluoromethoxy)carbanilohydrazide, (RS)-1-methyl-2-nitro-3-(tetrahydro-3-furylmethyl)guanidine, 3-iodo-2-propynyl butylcarbamate, 2-phenylphenol, and coal tar-based creosote oil.

[0036] Among the above-mentioned wood preservatives, for example, the triazole wood preservative (2RS,3RS;2RS,3SR)-2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol (e.g., cyproconazole commercially available from Fumakilla Total System Co., Ltd.), the neonicotinoid wood preservative 1-[(6-chloro-3-pyridinyl)methyl]-4,5-dihydro-N-nitro-1H-imidazole-2-ol (e.g., cyproconazole commercially available from Fumakilla Total System Co., Ltd.), and the neonicotinoid wood preservative 1-[(6-chloro-3-pyridinyl)methyl]-4,5-dihydro-N-nitro-1H-imidazole-2-ol (e.g., cyproconazole commercially available from Fumakilla Total System Co., Ltd.) are preferred. Amines (e.g., imidacloprid available from Lanxess K.K.), pyrethroid wood preservatives such as 2-(4-ethoxyphenyl)-2-methylpropyl-3-phenoxybenzyl ether (e.g., Etofenblox available from Mitsui Chemicals Agro Inc.), zinc naphthenate (e.g., a product available from Tokyo Chemical Industry Co., Ltd.), and copper naphthenate (e.g., a product available from Showa Chemical Co., Ltd.) are preferred from the standpoint of their performance as wood preservatives and their dispersibility and solubility in 1224 yd. The wood preservative agent may be used alone or in combination of two or more.

[0037] The content of the wood preservative agent is preferably 0.002 to 30 mass %, more preferably 0.01 to 20 mass %, based on the total mass of the wood preservative treatment solution.

[0038] The wood preservative treatment solution of the present disclosure may contain additives such as stabilizers and dispersants in addition to the organic solvents and wood preservative agents described above. The content of the additives is preferably 1% by mass or less based on the total mass of the wood preservative treatment solution.

[0039] The wood preservative may contain other ingredients for the purposes of adjusting viscosity or improving solubility in organic solvents for ease of handling. Specifically, the wood preservative may contain a surfactant or water. Examples of surfactants include nonionic surfactants, anionic surfactants, and cationic surfactants.

[0040] The water content is preferably 10% by mass or less, more preferably 5% by mass or less, even more preferably 3% by mass or less, based on the total mass of the wood preservative treatment solution, and particularly preferably substantially free. When the water content is within the above range, an increase in the moisture content of wood is suppressed when the wood preservative treatment solution is brought into contact with wood, thereby suppressing dimensional fluctuations of the wood. With regard to the water content, "substantially free" means that the water content is below the detection limit when measured by a known method that is common technical knowledge in the relevant technical field.

[0041] <Penetration of wood preservative treatment solution> Next, the permeability of the wood preservative treatment solution of the present disclosure into wood will be described. When the permeability of the wood preservative treatment solution of the present disclosure into wood is measured based on the permeability test described below, the ratio of post-treatment wood mass to pre-treatment wood mass is preferably 3.0 or greater. In the permeability test described below, this ratio is preferably 3.0 or greater when the pressure inside the pressure-resistant vessel is 0.05 MPaG or 0.10 MPaG, and more preferably 3.0 or greater when the pressure inside the pressure-resistant vessel is both 0.05 MPaG and 0.10 MPaG. By satisfying this ratio, it is possible to produce wood preservative-treated wood in which the wood preservative has sufficiently infiltrated into the interior of the wood. (Permeability test) A piece of cedar wood measuring 15mm thick x 15mm wide x 50mm long is placed in a glass tube, and an amount of wood preservative treatment solution is poured into the glass tube so that the entire piece of wood is immersed. The glass tube is then placed in a pressure-resistant container and sealed, and the pressure inside the pressure-resistant container is pressurized using compressed air to 0.05 MPaG or 0.10 MPaG, and left to stand for 30 minutes in an environment at 25°C. The wood piece is then removed from the container, and the ratio of the post-treatment wood mass (the mass of the wood immediately after removal) to the pre-treatment wood mass (the mass of the wood piece before the permeability test) is calculated for both cases where the pressure inside the pressure-resistant container is 0.05 MPaG and 0.10 MPaG.

[0042] <Method of manufacturing wood with wood preservatives> Next, the method for producing wood coated with a wood preservative of the present disclosure will be described. The method for producing wood preservative-treated wood of the present disclosure is a method for producing wood preservative-treated wood by contacting the wood with the wood preservative treatment solution of the present disclosure and volatilizing the organic solvent. By contacting the wood with the wood preservative treatment solution of the present disclosure, the wood preservative treatment solution of the present disclosure penetrates into the wood.

[0043] Methods for contacting wood with the wood preservative solution of the present disclosure include brushing the wood preservative solution onto the wood surface, spraying the wood preservative solution onto the wood surface, immersing the wood in the wood preservative solution, applying pressure to the wood while immersed in the wood preservative solution, etc. Of these, applying pressure to the wood while immersed in the wood preservative solution is preferred. The wood preservative in the wood preservative treatment solution is preferably dissolved in the organic solvent containing 1224yd. Therefore, by the above-mentioned treatment, the wood preservative adheres to the surface of the wood together with the organic solvent containing 1224yd and then penetrates into the wood from near the surface. The organic solvent is then volatilized and removed from the inside of the wood by heating the wood, leaving it at room temperature, or reducing the pressure. When such organic solvents are removed by volatilization from within the wood, the organic solvent may dissolve in the water in the wood, reducing the removal efficiency. From this point of view, the 1224yd Z-isomer, which has low solubility in water, is preferred.

[0044] Among the above methods, a treatment method in which wood is immersed in a wood preservative treatment solution and pressure is applied to penetrate the wood into the wood can be used, for example, the method disclosed in Japanese Patent No. 4149422. Even when used in a treatment device such as that described in Japanese Patent No. 4149422, the 1224yd used in the present disclosure is a volatile liquid with a boiling point of 10 to 30°C at normal pressure, and therefore can be easily recovered by evaporation and condensation. Furthermore, because the wood preservative treatment method disclosed in Japanese Patent No. 4149422 is generally performed in a closed system, there are cases in which the wood preservative treatment solution is transferred between a wood treatment container and a storage container, such as a tank, for storing the wood preservative treatment solution. In such cases, since the wood preservative treatment solution disclosed herein has a vapor pressure equal to or greater than atmospheric pressure at room temperature, it is easy to create a pressure difference between the containers by controlling the pressure and temperature. For example, when transferring the wood preservative treatment solution by applying pressure to the containers, the pressure difference is smaller than when using an organic solvent that is below atmospheric pressure at room temperature. Alternatively, when transferring the wood preservative treatment solution by heating or cooling either or both of the treatment container and the storage container, the pressure difference between the containers is larger than when using an organic solvent that is below atmospheric pressure at room temperature, allowing the wood preservative treatment solution to be transferred by temperature control alone. The pressure control and the temperature control may be combined. This allows the wood preservative treatment solution to move easily due to the pressure difference of 1224 yd, thereby reducing the energy required for transport by the transport pump. Furthermore, from the perspective of recovering organic solvents released from wood impregnated with a wood preservative treatment solution, the 1224yd used in this disclosure, which has a boiling point of 15°C, easily volatilizes from wood, so the amount released into the environment can be reduced by devising a recovery device. Furthermore, because 1224yd itself has little impact on the environment, even if it is released into the environment, the environmental impact can be reduced compared to the release of other organic solvents. [Example]

[0045] An embodiment of the present disclosure will be described in more detail below using examples, but the present disclosure is not limited thereto. Example 1 corresponds to an example, and Example 2 corresponds to a comparative example.

[0046] HCFO-1224yd was produced as an isomer mixture of HCFO-1224yd(E) and HCFO-1224yd(Z) according to the method described in WO 2017 / 110851. The isomer mixture was purified by the method described in WO 2017 / 146190 to produce HCFO-1224yd(E) and HCFO-1224yd(Z). The HCFO-1224yd used in the examples was mixed so that the mass ratio represented by HCFO-1224yd(Z) / HCFO-1224yd(E) was 99 / 1, and purified HCFO-1224yd with a purity of 99.5% was obtained. In the following tests, the purified 1224yd will be referred to as 1224yd.

[0047] The Z isomer of 1233zd was synthesized by the method described in JP 2013-87066 A. Specifically, crude 1233zd(Z) containing 3-chloro-1,1,1,3-tetrafluoropropane (HCFC-244fa), 2-chloro-1,1,1,3,3-pentafluoropropane (HCFC-235da), and 1233zd(Z) was mixed with triethylamine and reacted at 150°C for 3 hours to obtain a reaction product containing 1233zd(Z). This reaction product was further purified to obtain purified 1233zd(Z) with a purity of 99.5%. In the following tests, this purified 1233zd(Z) will be referred to as 1233zd(Z).

[0048] The wood preservative used was a zinc naphthenate-mineral spirit solution (Zn: 8%) manufactured by Fujifilm Wako Pure Chemical Industries, Ltd.

[0049] <Examples 1-2> The above wood preservative agents were dissolved in the respective solvents shown in Table 1 to prepare wood preservative treatment solutions.

[0050] <Penetration test> The prepared wood preservative treatment solution was used to immerse wood in the following manner. A piece of cedar wood, 15 mm thick x 15 mm wide x 50 mm long, cut from a 15 mm thick wooden board was placed in a glass tube and the wood preservative treatment solution of Example 1 or 2 was poured into it. The tube was then placed in a pressure-resistant container, sealed, and the pressure in the pressure-resistant container was increased with compressed air to the pressure shown in Table 1, and the container was left to stand for 30 minutes. Thereafter, the wood preservative treatment solution in the pressure vessel was transferred to another vessel for recovery, and the pressure in the pressure vessel was released to atmospheric pressure, yielding wood with the wood preservative agent before drying. The change in the mass of the wood preservative-treated wood obtained by the above method immediately after removal from the pressure vessel before drying (post-treatment wood mass) and the initial mass before the impregnation treatment (pre-treatment wood mass) was taken as the penetration performance of the wood preservative treatment solution and evaluated according to the following criteria: The larger the ratio of post-treatment wood mass / pre-treatment wood mass below, the more wood preservative treatment solution has penetrated into the wood, indicating a higher penetration ability of the wood preservative treatment solution into the wood. A: The ratio of wood mass after treatment to wood mass before treatment is 3.0 or more B: The ratio of wood mass after treatment to wood mass before treatment is 2.5 or more and less than 3.0 C: The ratio of wood mass after treatment to wood mass before treatment is less than 2.5

[0051] [Table 1]

[0052] The results are shown in Table 1. It was confirmed that the wood preservative treatment solution of the present disclosure has excellent penetration into wood. Furthermore, when a permeability test was carried out in the same manner as in Example 1 except that copper naphthenate was used instead of zinc naphthenate, the same results as in Example 1 were obtained. Furthermore, by drying the wood preservative-coated wood obtained in the <Penetration Test> before drying and removing the organic solvent, it was possible to produce wood preservative-coated wood in which the wood preservative had been sufficiently infiltrated into the interior of the wood.

[0053] The disclosure of Japanese Patent Application No. 2021-097391, filed on June 10, 2021, is incorporated herein by reference in its entirety. All documents, patent applications, and technical standards mentioned herein are incorporated herein by reference to the same extent as if each individual document, patent application, and technical standard was specifically and individually indicated to be incorporated by reference.

Claims

1. A wood preservative treatment solution comprising an organic solvent containing 1-chloro-2,3,3,3-tetrafluoropropene and a wood preservative agent.

2. 2. The wood preservative treatment solution according to claim 1, wherein the content of the 1-chloro-2,3,3,3-tetrafluoropropene is 50% by mass or more based on the total mass of the organic solvent.

3. 3. The wood preservative treatment solution according to claim 1, wherein the content of the organic solvent is 70 to 99.998% by mass based on the total mass of the wood preservative treatment solution.

4. The 1-chloro-2,3,3,3-tetrafluoropropene includes the Z isomer of 1-chloro-2,3,3,3-tetrafluoropropene and the E isomer of 1-chloro-2,3,3,3-tetrafluoropropene, The wood preservative treatment solution according to any one of claims 1 to 3, wherein the content of the Z isomer of 1-chloro-2,3,3,3-tetrafluoropropene is 50% by mass or more based on the total amount of the Z isomer of 1-chloro-2,3,3,3-tetrafluoropropene and the E isomer of 1-chloro-2,3,3,3-tetrafluoropropene.

5. The wood preservative treatment solution according to any one of claims 1 to 4, wherein the wood preservative is at least one selected from ammonium-based wood preservatives, triazole-based wood preservatives, neonicotinoid-based wood preservatives, phenylpyrazole-based wood preservatives, phenylpyrrole-based wood preservatives, benzoylphenylurea-based wood preservatives, anthranilic diamide-based wood preservatives, strobilurin-based wood preservatives, pyrethroid-based wood preservatives, and copper or zinc salts of fatty acids and fatty acids having an aromatic ring.

6. The wood preservative treatment solution according to any one of claims 1 to 4, wherein the wood preservative is at least one selected from the group consisting of triazole wood preservatives, neonicotinoid wood preservatives, pyrethroid wood preservatives, and copper or zinc salts of fatty acids and fatty acids having an aromatic ring.

7. The wood preservative treatment solution according to any one of claims 1 to 4, wherein the wood preservative agent is at least one selected from the group consisting of (2RS,3RS;2RS,3SR)-2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol, 1-[(6-chloro-3-pyridinyl)methyl]-4,5-dihydro-N-nitro-1H-imidazol-2-amine, 2-(4-ethoxyphenyl)-2-methylpropyl-3-phenoxybenzyl ether, zinc naphthenate, and copper naphthenate.

8. 8. The wood preservative treatment solution according to claim 1, wherein the content of the wood preservative agent is 0.002 to 30% by mass based on the total mass of the wood preservative treatment solution.

9. The wood preservative treatment solution according to any one of claims 1 to 8, wherein the wood preservative treatment solution is substantially free of water or contains 10% by mass or less of water relative to the total mass of the wood preservative treatment solution.

10. The wood preservative treatment solution according to any one of claims 1 to 9, wherein, when the ratio of the mass of wood after treatment to the mass of wood before treatment is measured based on the following permeability test, the ratio is 3.0 or more both when the pressure inside the pressure-resistant container is 0.05 MPaG and when it is 0.10 MPaG. (Permeability test) A piece of cedar wood measuring 15 mm thick x 15 mm wide x 50 mm long was placed in a glass tube, and an amount of wood preservation treatment solution was poured into the glass tube so that the entire piece of wood was immersed. The glass tube was then placed in a pressure-resistant container and sealed, and the pressure inside the pressure-resistant container was pressurized using compressed air to 0.05 MPaG or 0.10 MPaG. The container was then left to stand for 30 minutes in an environment at 25°C, after which the piece of wood was removed, and the ratio of the mass of the piece of wood immediately after removal (post-treatment wood mass) to the mass of the piece of wood before the permeability test (pre-treatment wood mass) was calculated for both the case where the pressure inside the pressure-resistant container was 0.05 MPaG and the case where the pressure inside the pressure-resistant container was 0.10 MPaG.

11. A method for producing wood preservative-treated wood, comprising contacting wood with the wood preservative treatment solution according to any one of claims 1 to 10 and volatilizing the organic solvent to produce the wood preservative-treated wood.

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