Method for producing porous body

Abstract

To provide a method for producing a porous body with higher productivity.SOLUTION: There is provided a method for producing a porous body which comprises: preparing a solution containing a di- or more-functional polymerizable monomer and a solvent compatible with the polymerizable monomer and containing no polymerization initiator; radicalizing directly the polymerizable monomer contained in the solution to polymerize the polymerizable monomer to form a phase separated product containing a porous body and the solvent from the solution; and vaporizing the solvent contained in the phase separated product. The solvent includes a predetermined solvent such as diethylene glycol diethylether.SELECTED DRAWING: None

Description

[Technical field]

[0001] The present disclosure relates to a method for producing a porous body and the porous body. [Background technology]

[0002] Polymeric porous bodies (hereinafter simply referred to as "porous bodies") are used in various fields. For example, porous bodies are used as foams (e.g., cushioning materials, etc.), separation membranes (e.g., water treatment, etc.), porous membranes (e.g., battery separators, etc.), and reflective substrates (e.g., lighting fixtures, etc.).

[0003] Patent Document 1 discloses a method for forming a porous body. In the method disclosed in Patent Document 1, a composition containing a binder resin, a photosensitive compound, and a photopolymerization initiator is applied onto a substrate to form a coating film. Next, the coating film is irradiated with ultraviolet light according to a desired pattern using an ultra-high pressure mercury lamp. Next, the coating film is immersed in a poor solvent for the binder resin. Next, the poor solvent that has penetrated into the inside of the coating film is volatilized. This results in a porous body. [Prior art documents] [Patent documents]

[0004] [Patent Document 1] JP 2004-143427 A Summary of the Invention [Problem to be solved by the invention]

[0005] However, in the formation method disclosed in Patent Document 1, the ultraviolet irradiation time is about 1 to 2 minutes. Therefore, there is a demand for a manufacturing method of a porous body that can manufacture a porous body in a shorter time (in other words, has superior productivity).

[0006] The present disclosure has been made in consideration of the above circumstances. An object of one embodiment of the present disclosure is to provide a method for producing a porous body with excellent productivity, and a porous body. [Means for solving the problem]

[0007] As a result of intensive research into the above-mentioned problems, the present inventors have experimentally found that by using an electron beam, which has a higher energy level than ultraviolet light, and by appropriately selecting a combination of the type of polymerizable monomer and the type of solvent, it is possible to produce a porous body in a shorter time than in the past. Based on this finding, the present inventors have completed the present invention.

[0008] Means for solving the above problems include the following embodiments. <1> preparing a solution containing a di- or higher functional polymerizable monomer and a solvent compatible with the polymerizable monomer, but not containing a polymerization initiator; directly radicalizing the polymerizable monomer contained in the solution to polymerize the polymerizable monomer, thereby forming a phase-separated product containing a porous body and the solvent from the solution; Vaporizing the solvent contained in the phase separated product; Including, The solvent includes at least one selected from diethylene glycol diethyl ether, 2-methoxyethanol, dimethylacetamide, ethylene glycol diacetate, γ-butyrolactone, propylene carbonate, dimethylformamide, tetradecane, 1-hexanol, 1-decanol, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, triethylene glycol monomethyl ether, ethanol, 2-propyl alcohol, 1-propyl alcohol, 1-methoxy-2-propanol, 2-ethoxyethanol, dimethyl sulfoxide, hexylene glycol, 1,4-dioxane, sulfolane, acetonitrile, dimethylethyleneurea, tetraethylene glycol dimethyl ether, triethylene glycol monomethyl ether, ethyl glycol acetate, and 2-pyrrolidone. <2> In forming the phase-separated product, the solution is irradiated with an electron beam to directly convert the polymerizable monomer into a radical. <1> A method for producing the porous body according to claim 1. <3> The electron beam irradiation is performed so that the absorbed dose is 10 kGray to 200 kGray. <2> A method for producing the porous body according to claim 1. <4> In preparing the solution, the content of the polymerizable monomer is 5% by mass to 50% by mass with respect to the total amount of the polymerizable monomer and the solvent. <1> ~ <3> 13. A method for producing a porous body according to any one of the above items. <5> A porous material having structural units derived from difunctional or higher functional polymerizable monomers and containing no polymerization initiator. Effect of the Invention

[0009] According to the present disclosure, a method for producing a porous body with excellent productivity and a porous body are provided. [Brief description of the drawings]

[0010] [Figure 1] FIG. 1 is a scanning electron microscope (SEM) photograph (magnification: 10,000 times) of the surface of the porous body of Example 1. [Diagram 2] FIG. 2 is an SEM photograph (magnification: 10,000 times) of the surface of the porous body of Example 3. [Diagram 3] FIG. 3 is an SEM photograph (magnification: 10,000 times) of the surface of the porous body of Example 4. [Figure 4] FIG. 4 is an SEM photograph (magnification: 10,000 times) of the surface of the porous body of Example 5. [Diagram 5] FIG. 5 is a scanning electron microscope (SEM) photograph (magnification: 10,000 times) of the surface of the porous body of Example 32. [Figure 6] FIG. 6 is a scanning electron microscope (SEM) photograph (magnification: 10,000 times) of the surface of the porous body of Comparative Example 29. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0011] In the present disclosure, a numerical range indicated using "~" means a range including the numerical values ​​described before and after "~" as the minimum and maximum values, respectively. In the numerical ranges described in stages in the present disclosure, the upper limit or lower limit described in a certain numerical range may be replaced with the upper limit or lower limit of another numerical range described in stages. In the numerical ranges described in the present disclosure, the upper limit or lower limit described in a certain numerical range may be replaced with a value shown in the Examples. In the present disclosure, a combination of two or more preferred embodiments is a more preferred embodiment. In the present disclosure, the amount of each component means the total amount of the multiple substances unless otherwise specified, when there are multiple substances corresponding to each component. In the present disclosure, the term "process" includes not only an independent process, but also a process that cannot be clearly distinguished from other processes, as long as the intended purpose of the process is achieved. In the present disclosure, "(meth)acrylate" refers to at least one of acrylate and methacrylate, and "(meth)acryloyl group" refers to at least one of acryloyl group and methacryloyl group.

[0012] (1) Method for producing porous body The method for producing a porous body of the present disclosure includes preparing a solution containing a difunctional or higher functional polymerizable monomer and a solvent compatible with the polymerizable monomer, but not containing a polymerization initiator (hereinafter also referred to as the "preparation process"); directly radicalizing the polymerizable monomer contained in the solution, polymerizing the polymerizable monomer, and forming a phase-separated product containing a porous body and the solvent from the solution (hereinafter also referred to as the "formation process"); and vaporizing the solvent contained in the phase-separated product (hereinafter also referred to as the "vaporization process"). The solvent includes at least one selected from diethylene glycol diethyl ether, 2-methoxyethanol, dimethylacetamide, ethylene glycol diacetate, γ-butyrolactone, propylene carbonate, dimethylformamide, tetradecane, 1-hexanol, 1-decanol, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, triethylene glycol monomethyl ether, ethanol, 2-propyl alcohol, 1-propyl alcohol, 1-methoxy-2-propanol, 2-ethoxyethanol, dimethyl sulfoxide, hexylene glycol, 1,4-dioxane, sulfolane, acetonitrile, dimethylethyleneurea, tetraethylene glycol dimethyl ether, triethylene glycol monomethyl ether, ethyl glycol acetate, and 2-pyrrolidone (hereinafter, also referred to as "predetermined solvent").

[0013] "Polymerizable monomer" refers to a monomer containing an ethylenically unsaturated group. "Bifunctional or higher" refers to having two or more ethylenically unsaturated groups in one molecule. "Polymerization initiator" refers to a compound (excluding monomers) that generates radicals when irradiated with active energy rays (e.g., electromagnetic waves, radiation, etc.). Polymerization initiators include known polymerization initiators used in ultraviolet curing. "Does not contain polymerization initiator" refers to the content of polymerization initiator being 0.001 mass% or less with respect to the total amount of the solution, including the case where the content of polymerization initiator is 0 mass%. "Directly radicalizes polymerizable monomer" refers to the polymerization of polymerizable monomer proceeds even without the generation of radicals by polymerization initiator by irradiation with radiation (e.g., electron beam, X-ray, gamma ray, etc.). "Solution" refers to a liquid phase in which the two are homogeneously dissolved. "Porous body" refers to a polymer (solid phase) of polymerizable monomer.

[0014] The method for producing a porous body according to the present disclosure has the above-mentioned configuration and is therefore more productive.

[0015] (1.1) Preparation process In the preparation step, a solution is prepared which contains a di- or higher functional polymerizable monomer and a solvent compatible with the polymerizable monomer but does not contain a polymerization initiator.

[0016] The solution contains a difunctional or higher functional polymerizable monomer. The difunctional or higher functional polymerizable monomer preferably contains a (meth)acrylate having two or more (meth)acryloyl groups, and is preferably a (meth)acrylate having two or more (meth)acryloyl groups. Examples of bifunctional polymerizable monomers include tricyclodecane dimethanol di(meth)acrylate, ethylene oxide (EO) modified trimethylolpropane tri(meth)acrylate, and propylene oxide (PO) modified trimethylolpropane tri(meth)acrylate. Examples of trifunctional or higher polymerizable monomers include trimethylolpropane tri(meth)acrylate, pentaerythritol tetra(meth)acrylate, tris(acryloxyethyl)isocyanurate, dipentaerythritol hexa(meth)acrylate, and dipentaerythritol hydroxypenta(meth)acrylate. These may be used alone or in combination of two or more.

[0017] The solution contains a predetermined solvent, and preferably contains at least one selected from diethylene glycol diethyl ether, 2-methoxyethanol, dimethylacetamide, ethylene glycol diacetate, γ-butyrolactone, propylene carbonate, dimethylformamide, tetradecane, 1-hexanol, 1-decanol, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, triethylene glycol monomethyl ether, ethanol, 2-propyl alcohol, 1-propyl alcohol, 1-methoxy-2-propanol, and 2-ethoxyethanol.

[0018] The content of the polymerizable monomer (hereinafter also referred to as "monomer ratio") is not particularly limited, and is preferably 5% by mass to 50% by mass, more preferably 10% by mass to 40% by mass, and further preferably 10% by mass to 25% by mass, based on the total amount of the polymerizable monomer and the solvent. If the monomer ratio is within the range of 5% by mass to 50% by mass, the desired porous body is easily obtained.

[0019] The solution does not contain a polymerization initiator. The solution may contain additives or may not contain additives in addition to the difunctional or higher polymerizable monomer and the solvent. Examples of additives include dispersants, adhesion promoters such as silane coupling agents, antioxidants, anti-aggregation agents, antifoaming agents, and surfactants.

[0020] (1.2) Formation process In the forming step, the polymerizable monomer contained in the solution is directly radicalized to polymerize the polymerizable monomer, thereby forming a phase-separated product containing a porous body and the solvent from the solution.

[0021] The method of directly radicalizing the polymerizable monomer is not particularly limited, and examples thereof include a method of irradiating a solution with radiation (e.g., electron beam, X-ray, gamma ray, etc.). Among them, it is preferable to irradiate a solution with an electron beam to directly radicalize the polymerizable monomer. This allows the polymerization of the polymerizable monomer to proceed in a shorter time than conventional methods such as ultraviolet curing. When the polymerizable monomer is directly radicalized, the solution may be in the form of a coating applied onto the surface of a substrate.

[0022] The electron beam irradiation is not particularly limited, but is preferably performed so that the absorbed dose is 10 kGray to 200 kGray, which makes it easier to obtain the desired porous body. The absorbed dose of the electron beam is not particularly limited, but is more preferably 30 kGy to 100 kGy, and further preferably 30 kGy to 80 kGy. The acceleration voltage of the electron beam may be appropriately adjusted depending on the size of the porous body, and may be 80 kV to 300 kV.

[0023] (1.3) Vaporization process In the vaporization step, the solvent contained in the phase-separated product is vaporized.

[0024] The method for vaporizing the solvent is not particularly limited, and examples thereof include heat drying, reduced pressure drying, freeze drying, etc. In heat drying, if the heating temperature is equal to or lower than the glass transition temperature of the polymerizable monomer or its polymer, the solvent can be removed from the phase-separated product without destroying the porous structure of the porous body. Examples of heat drying include radiant heat drying using an infrared heater and air drying using a blower.

[0025] (2) Porous material The porous body of the present disclosure has constitutional units derived from difunctional or higher functional polymerizable monomers and does not contain a polymerization initiator.

[0026] "Containing no polymerization initiator" means that the content of the polymerization initiator is 0.001% by mass or less relative to the total amount of the porous body, and includes the case where the content of the polymerization initiator is 0% by mass.

[0027] The porous body of the present disclosure is preferably a porous body manufactured by the method for manufacturing a porous body of the present disclosure. The bifunctional or higher polymerizable monomer is the same as the compound exemplified as the bifunctional or higher polymerizable monomer in the method for manufacturing a porous body. The size of the porous body is not particularly limited and is appropriately selected according to the application of the porous body.

[0028] The porous body is suitably used for, for example, foams (such as cushioning materials), separation membranes (such as water treatment), porous membranes (such as battery separators), and reflective substrates (such as lighting fixtures). EXAMPLES

[0029] The present disclosure will be described in more detail below with reference to examples, but the invention of the present disclosure is not limited to these examples.

[0030] [1] Example 1 [1.1] Preparation process As a polymerizable monomer, tricyclodecane dimethanol diacrylate (functional group number: 2) was prepared, and as a solvent, diethylene glycol diethyl ether was prepared. The polymerizable monomer and the solvent were placed in a sample bottle. The monomer ratio was 30 mass %. The sample bottle was shaken by hand to stir the polymerizable monomer and the solvent, and a solution was obtained.

[0031] The sample bottle was left to stand, the solution was visually observed, and the compatibility was evaluated according to the following criteria: An acceptable compatibility evaluation result is "A1". "A1": No separation between the polymerizable monomer and the solvent was observed. "B1": Separation of the polymerizable monomer and the solvent was observed. "A1" can be evaluated as the polymerizable monomer and the solvent being compatible with each other. "B1" can be evaluated as the polymerizable monomer and the solvent being incompatible with each other.

[0032] In Example 1, the compatibility evaluation result was "A1".

[0033] [1.2] Forming process The solution was applied onto an aluminum foil by casting to form a coating film having a thickness of 350 μm. The coating film was irradiated with an electron beam to obtain an irradiated coating film. A belt conveyor type area beam type electron beam irradiation device was used for the electron beam irradiation. The acceleration voltage of the electron beam was 200 kV, and the absorbed dose was 50 kGy. The electron beam irradiation time was 1.2 seconds. The "electron beam irradiation time" indicates the time required for the coating film moving on the belt conveyor to pass through the electron beam irradiation area. The acceptable irradiation time is within 20 seconds.

[0034] The irradiated coating film was visually observed and the polymerization was evaluated according to the following criteria. An acceptable polymerization evaluation result is "A2". "A2": The color of the irradiated coating film was white. "B2": The color of the irradiated coating was transparent. "A2" can be evaluated as polymerization of the polymerizable monomer proceeding sufficiently to form a porous body. "B2" can be evaluated as polymerization of the polymerizable monomer not proceeding sufficiently to form a porous body.

[0035] In Example 1, the result of the polymerization evaluation was "A2," which means that the polymerization of the polymerizable monomer in the irradiated coating film had progressed sufficiently to form a porous body.

[0036] [1.3] Vaporization process The aluminum foil on which the irradiated coating film was formed was placed on a hot plate. The hot plate was set to a temperature of 120°C, and the irradiated coating film was heated at 120°C for about 2 minutes to volatilize and remove the solvent. This allowed the polymer to be separated from the irradiated coating film.

[0037] The surface of the polymer was observed using a scanning electron microscope (SEM) (magnification: 10,000 or 50,000 times), and the porosity of the polymer was evaluated according to the following criteria. The acceptable porosity evaluation result is "A3". "A3": Either isolated pores or continuous pores were confirmed. "B3": Neither isolated nor continuous pores were observed. "A3" indicates that the polymer is porous. "B3" indicates that the polymer is not porous.

[0038] In Example 1, the result of the porosity evaluation was "A3". In other words, it was found that the polymer was porous. Fig. 1 shows an SEM photograph (magnification: 10,000 times) of the surface of the porous body of Example 1.

[0039] [2] Examples 2 to 33, Comparative Examples 1 to 28 In Examples 2 to 33 and Comparative Examples 1 to 28, the preparation step, the formation step, and the vaporization step were carried out in the same manner as in Example 1, except that the polymerizable monomer, the solvent, the monomer ratio, the absorbed dose, and the irradiation time were changed as shown in Tables 1 to 3. The results of the compatibility evaluation, the polymerizability evaluation, and the porosity evaluation are shown in Tables 1 to 3. FIG. 2 shows an SEM photograph (magnification: 10,000 times) of the surface of the porous body of Example 3. FIG. 3 shows an SEM photograph (magnification: 10,000 times) of the surface of the porous body of Example 4. FIG. 4 shows an SEM photograph (magnification: 10,000 times) of the surface of the porous body of Example 1. FIG. 5 shows an SEM photograph (magnification: 10,000 times) of the surface of the porous body of Example 1.

[0040] [3] Comparative Example 29 [3.1] Preparation process As a polymerizable monomer, tricyclodecane dimethanol diacrylate (functional group number: 2) was prepared. As a solvent, triethylene glycol monomethyl ether was prepared. As a polymerization initiator, 1-hydroxycyclohexyl phenyl ketone (BASF's "Omnirad 184") was prepared. The polymerizable monomer, the solvent, and the polymerization initiator were mixed to obtain a solution, with a blending ratio (polymerizable monomer / solvent / polymerization initiator) of 19 parts by mass / 80 parts by mass / 1 part by mass.

[0041] [3.2] Forming process The solution was applied onto a substrate film (material: polyethylene terephthalate) using a spin coater, dried at 80°C for 15 minutes, and cooled to form a coating film. A cover film (material: polyethylene terephthalate) was attached to the coating film to obtain a resin sheet. The coating film thickness of the resin sheet was 100 μm. The resin sheet was irradiated with ultraviolet light, heated at 85°C for 2 minutes, and cooled to room temperature to obtain an irradiated resin sheet. An ultra-high pressure mercury lamp was used for the ultraviolet light irradiation. The irradiation intensity of the ultraviolet light was 220mW / cm 2 The ultraviolet irradiation time was 60 to 120 seconds. The polymerization property of the irradiated coating film contained in the irradiated resin sheet was evaluated. The results of the polymerization property evaluation are shown in Table 3.

[0042] [3.3] Vaporization process The cover film was peeled off from the irradiated resin sheet to obtain a coating sheet. The coating sheet was immersed in a methanol tank for 4 hours and then removed from the methanol tank. Next, a high-pressure mercury lamp was used to irradiate the surface side of the coating film and the substrate film side with 1000 mJ / cm2. 3 After irradiation, the film was left at room temperature overnight to evaporate the methanol, thereby obtaining a polymer formed on the substrate film. The porosity of the polymer was evaluated. The results of the porosity evaluation are shown in Table 3. Fig. 6 shows an SEM photograph (magnification: 10,000 times) of the surface of the porous body of Comparative Example 29.

[0043] [4] Comparative Examples 30 to 34 In Comparative Examples 30 to 34, the preparation step, formation step, and vaporization step were carried out in the same manner as in Comparative Example 29, except that the solvent was changed as shown in Table 3, and the compounding ratio (polymerizable monomer / solvent / polymerization initiator) in Comparative Examples 30, 32, and 34 was changed to 39 parts by mass / 60 parts by mass / 1 part by mass. The evaluation results of the polymerizability and porosity are shown in Table 3.

[0044] [Table 1]

[0045] [Table 2]

[0046] [Table 3]

[0047] In Tables 1 to 3, "Acrylic A" refers to tricyclodecane dimethanol diacrylate (number of functional groups: 2). "Acrylic B" refers to trimethylolpropane triacrylate (number of functional groups: 3). "Acrylic C" refers to isobornyl acrylate (number of functional groups: 1). "Initiator A" refers to 1-hydroxycyclohexyl phenyl ketone. "EB" refers to electron beam. "UV" refers to ultraviolet light. "Monomer ratio" refers to the ratio of polymerizable monomer to the total amount of polymerizable monomer and solvent.

[0048] The manufacturing methods of Examples 1 to 33 include a preparation step, a formation step, and a vaporization step, and the solvent includes a predetermined solvent. Therefore, in Examples 1 to 33, a porous body was obtained even when the electron beam irradiation time was within 20 seconds. As a result, it was found that the manufacturing methods of Examples 1 to 33 are porous body manufacturing methods with superior productivity.

[0049] Comparing Figures 1 and 3, no significant differences were observed on the surface of the porous body, and it was found that the higher the absorbed dose, the greater the number of pores on the surface of the porous body. 2 to 4, it was found that the number of pores on the surface of the porous body tends to decrease as the monomer ratio increases. Comparing Figures 1 to 4 with Figure 5, it was found that the porous body shown in Figure 5 has a structure in which a plurality of particulate materials are linked together. This shows that a porous body can be obtained even when a trifunctional polymerizable monomer is used.

[0050] The solvent did not contain the specified solvent in the manufacturing methods of Comparative Examples 1 to 11. Therefore, the polymerizability evaluation of Comparative Examples 1 to 11 was "B2." In the manufacturing methods of Comparative Examples 12 to 18, no bifunctional or higher polymerizable monomer was used. Therefore, the polymerizability evaluation of Comparative Examples 12 to 18 was "B2." It is presumed that the main reasons for this are that a crosslinked structure is unlikely to be formed with a monofunctional polymerizable monomer, and that the chain length of the polymer having a constitutional unit derived from the monofunctional polymerizable monomer is short. In the manufacturing methods of Comparative Examples 19 to 28, the solvent did not contain the specified solvent, and therefore the compatibility evaluation of Comparative Examples 19 to 28 was "B1." In the manufacturing methods of Comparative Examples 29 to 34, the solution contained a polymerization initiator, and irradiation with ultraviolet rays was performed instead of irradiation with electron beams in the formation step, so that the irradiation time of ultraviolet rays was more than 20 seconds. As a result, it was found that the manufacturing methods of Comparative Examples 1 to 34 are not manufacturing methods of porous bodies with superior productivity.

Claims

1. preparing a solution containing a di- or higher functional polymerizable monomer and a solvent compatible with the polymerizable monomer, but not containing a polymerization initiator; irradiating the solution with an electron beam to directly radicalize the polymerizable monomer contained in the solution and polymerize the polymerizable monomer to form a phase-separated product containing a porous body and the solvent from the solution; Vaporizing the solvent contained in the phase separated product; Including, the polymerizable monomer is tricyclodecane dimethanol di(meth)acrylate or trimethylolpropane tri(meth)acrylate; When the polymerizable monomer is tricyclodecane dimethanol di(meth)acrylate, the solvent is at least one selected from diethylene glycol diethyl ether, 2-methoxyethanol, ethylene glycol diacetate, dimethylformamide, 1-hexanol, 1-decanol, diethylene glycol monoethyl ether, triethylene glycol monomethyl ether, 1-propyl alcohol, 1-methoxy-2-propanol, and 2-ethoxyethanol; A method for producing a porous body, wherein when the polymerizable monomer is trimethylolpropane tri(meth)acrylate, the solvent is at least one selected from diethylene glycol diethyl ether and 2-ethoxyethanol.

2. The method for producing a porous body according to claim 1, wherein the electron beam is irradiated to an absorbed dose of 10 kGray to 200 kGray.

3. 3. The method for producing a porous body according to claim 1, wherein in preparing the solution, a content of the polymerizable monomer is 5% by mass to 50% by mass with respect to a total amount of the polymerizable monomer and the solvent.

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