Patent Application
20230249150
The present invention relates to a porous film, a method for manufacturing a porous film, a microlens array, a microreactor, and a bio-device.
Porous films are manufactured by combining various polymer materials and porosity forming technologies and are expected to be able to be applied to microlens arrays, cell culture substrates, and anti-adhesion films. Particularly, porous films with a hole diameter of about 100 to 1000 μm and a uniform hole diameter have attracted attention because these porous films can be applied to microlenses when substances with different refractive indices are introduced into vacancies thereof or can selectively separate or support substances in this size range.
Examples of a method for manufacturing this kind of porous film include laser processing or photolithography using an optical device (for example, refer to Non-Patent Document 1), a top-down method such as cutting using a drill (for example, refer to Non-Patent Document 2), or a bottom-up method using self-organization such as a solvent casting method (for example, refer to Non-Patent Document 3). Manufacturing methods using the laser processing or photolithography are processes which basically merely perform two-dimensional patterning and incur high manufacturing costs when holes in this size range are processed with a larger area. Furthermore, in fine hole processing using a drill, there is a problem that it is difficult to finish the burrs generated on an outlet side.
On the other hand, the method using self-organization can perform mass production at low cost compared with the laser processing, photolithography, or the like using the optical device. Furthermore, Patent Document 1 describes a technique of forming condensation on a casting film to form water droplets and then evaporating a solvent and the water droplets from the casting film to form a porous film.
However, in the method using self-organization such as the solvent casting method described above or the method described in Patent Document 1, fine holes of about 100 nm to 20 μm can be formed, but holes with a hole diameter of about 100 to 1000 μm cannot be formed. Furthermore, it can be expected that a film with a hole diameter of about 100 to 1000 μm having not only two-dimensional but also three-dimensional porous structures would be able to be applied as a scaffolding material capable of allowing adhesion and proliferation of cells of several to several tens of μm in the holes. Therefore, it is required that a porous film with a hole diameter of about to 2000 μm be able to be manufactured from various types of material at low cost.
The present invention was made in view of the above-described circumstances, and an object of the present invention is to provide a porous film, a method for manufacturing a porous film, a microlens array, a microreactor, and a bio-device capable of manufacturing a porous film having hole sections with a diameter of 10 μm or more and 2000 μm or less at low cost.
The inventors of the present invention carried out intensive research, and as a result, found the excellent effect that, when a first step of preparing droplets which are formed from a first liquid into spheres with a predetermined diameter of 10 μm or more and 2000 μm or less and a second liquid which includes a photocuring agent and includes the droplets dispersed therein, a second step of injecting the droplets and the second liquid into a gap between a pair of substrates having optical transparency, a third step of curing the second liquid by irradiation with light through the substrates to form an external phase, and a fourth step of removing the droplets in the external phase to form hole sections are provided, a high quality porous film which have hole sections with a diameter of 10 μm or more and 2000 μm or less and have low manufacturing costs and a method for manufacturing the porous film can be provided and have completed the present invention.
That is to say, in order to solve the above object, the present invention adopts the following means.
(1) A first step of preparing droplets which are formed from a first liquid into spheres with a predetermined diameter of 10 μm or more and 2000 μm or less and a second liquid which includes a curing agent which cures by imparting energy or a curing agent which cures due to change in pH and includes the droplets dispersed therein; a second step of injecting the droplets and the second liquid into a gap between a pair of substrates; a third step of curing the second liquid to form a base; and a fourth step of removing the droplets in the base to form hole sections are provided.
(2) In the method for manufacturing a porous film according to (1), the second liquid may include a surfactant and a stabilizer.
(3) In the method for manufacturing a porous film according to (1) or (2), the energy may be light or heat.
(4) In the method for manufacturing a porous film according to any one of (1) to (3), a specific gravity of the first liquid may be larger than a specific gravity of the second liquid.
(5) In the method for manufacturing a porous film according to any one of (1) to (4), the distance between the pair of substrates may be adjusted so that the droplets are arranged in one layer in the gap.
(6) In the method for manufacturing a porous film according to any one of (1) to (4), the droplets may be arranged in a plurality of layers in the gap.
(7) In the method for manufacturing a porous film according to (6), the droplets may be arranged in a body-centered cubic structure.
(8) In the method for manufacturing a porous film according to (6), the droplets may be arranged in a hexagonal close-packed structure.
In the method for manufacturing a porous film according to (6), the droplets may be arranged in a face-centered cubic structure.
In the method for manufacturing a porous film according to any one of (1) to (9), in the first step, droplets of a plurality of types with different diameters may be prepared.
In the method for manufacturing a porous film according to any one of (1) to (10), the first step may include a step of causing the first liquid to flow into a flow path of a first tube and causing the droplets of the first liquid to flow from a nozzle of the first tube into the second liquid flowing through a flow path of a second tube.
In the method for manufacturing a porous film according to (11), at least one of a relative rate of the first liquid flowing through the first tube with respect to a rate of the second liquid flowing through the second tube and a diameter of the nozzle may be adjusted depending on a diameter of the droplets to be prepared.
In the method for manufacturing a porous film according to any one of (1) to (12), at least one of the first liquid and the second liquid may be an oil phase and the other thereof may be an aqueous phase.
In the method for manufacturing a porous film according to any one of (1) to (13), the step of removing the droplets may include a step of cleaning the droplets.
In the method for manufacturing a porous film according to any one of (1) to (14), the droplets may be formed with a predetermined diameter of 250 μm or more and 2000 μm or less.
(16) A porous film according to an aspect of the present invention includes: a plurality of hole sections formed in a spherical shape with a predetermined diameter of 10 μm or more and 2000 μm or less; and a base including a curing agent which cures by imparting energy or a curing agent which cures due to change in pH, wherein the plurality of hole sections are arranged with a predetermined size and a relative error in a diameter thereof is 6% or less.
(17) In the porous film according to (16), the base may include a surfactant and a stabilizer.
(18) In the porous film according to (16) or (17), the hole sections arranged to be adjacent to each other may communicate with each other via communication holes.
(19) In the porous film according to any one of (16) to (18), the plurality of hole sections may be arranged in a body-centered cubic structure.
(20) In the porous film according to any one of (16) to (18), the plurality of hole sections may be arranged in a hexagonal close-packed structure.
(21) In the porous film according to any one of (16) to (18), the plurality of hole sections may be arranged in a face-centered cubic structure.
(22) In the porous film according to any one of (16) to (21), the plurality of hole sections may include a plurality of first hole sections formed with a first diameter and a plurality of second hole sections formed with a second diameter different from the first diameter, and the first hole sections and the second hole sections may be arranged in a predetermined regular manner and relative errors in diameters thereof are 6% or less.
(23) In the porous film according to any one of (16) to (22), the hole sections may be formed with a predetermined diameter of 250 μm or more and 2000 μm or less.
(24) A microlens array according to an aspect of the present invention includes: the porous film according to any one of (16) to (23); and lens bodies arranged in the hole sections.
(25) A microreactor according to an aspect of the present invention includes: the porous film according to any one of (16) to (23).
(26) A bio-device according to an aspect of the present invention includes: the porous film according to any one of (16) to (23). [Advantageous Effects of Invention]
According to a method for manufacturing a porous film associated with an aspect of the present invention, a porous film having hole sections with a diameter of 10 μm or more and 2000 μm or less can be manufactured with low manufacturing costs and high quality.
According to a porous film associated with an aspect of the present invention, a high quality porous film having hole sections with a diameter of 10 μm or more and 2000 μm or less can be obtained with low manufacturing costs.
Embodiment modes of a porous film, a method for manufacturing a porous film, a microlens array, a microreactor, and a bio-device according to this embodiment will be described below with reference to
(First Embodiment of Porous Film)
First, a porous film 1 in a first embodiment will be described with reference to
As shown in
The hole sections 10 are formed in a spherical shape with a predetermined diameter and arranged in a single layer in a thickness direction of the porous film 1. A plurality of rows of the hole sections 10 whose center positions are aligned on a straight line are regularly arranged in a plane direction of the porous film 1. The hole sections are arranged in a zigzag shape in which neighboring rows are shifted by distances of the radius (a half-pitch) of the hole sections 10. The diameter of the hole sections 10 is set to 10 μm or more and 2000 μm or less, preferably 250 μm or more and 2000 μm or less.
The hole sections 10 arranged adjacent to each other communicate with each other via communication holes 11. The hole sections 10 have holes 12 at joint portions between the hole sections 10 and the glass substrate 31. The hole sections 10 have holes 13 at joint portions between the hole sections 10 and the glass substrate 32.
(Method for Manufacturing Porous Film 1)
Next, a method for manufacturing the porous film 1 in the above constitution will be described with reference to
(First Step)
As shown in
As shown in
In the present embodiment, an oil phase liquid is used as the first liquid L1. For example, a liquid which includes polydimethylsiloxane and bromobenzene bromobenzene added as a stabilizer for oil droplets (with a volume ratio of 79/21) may be used as the first liquid L1.
An aqueous phase liquid is used as the second liquid L2. For example, a liquid containing water (8.26×10% by weight), an acrylamide (8.26% by weight) as a monomer, N,N′-methylenebisacrylamide (8.26×10−1% by weight) as a crosslinking agent, an alkylphenone-based photopolymerization initiator (IRGACURE (registered trademark) 2959) (8.26×10−2% by weight) as a photopolymerization initiator, and polyvinyl alcohol (8.26% by weight) as a surfactant may be used as the second liquid L2. In the present embodiment, an initiator which performs curing by imparting light energy as energy to be imparted is used. Water is degassed for 15 minutes, purged with nitrogen for 15 minutes, and then used.
In the present embodiment, a specific gravity of the first liquid L1 is larger than a specific gravity of the second liquid L2. Since the second liquid L2 in the embodiment is an aqueous phase and most of the mass thereof is water, the specific gravity thereof is substantially 1. For this reason, a material with a specific gravity larger than 1 is selected as the first liquid L1.
(a) of
As shown in (a) to (e) of
Also, in the embodiment, since a specific gravity of the first liquid L1 is larger than a specific gravity of the second liquid L2, when the first liquid L1 is caused to flow into the second liquid L2, oil droplets D with a small relative error in particle diameter can be prepared without a problem that the first liquid L1 floats with respect to the second liquid L2 and spherical oil droplets D are not able to be stably formed.
(Second Step)
Next, a second step will be described.
In the second step, first, the number of stacked sheets of the sheet members 34 is adjusted in order to adjust a distance between the glass substrates 31 and 32 to a distance according to a particle diameter of the oil droplets D prepared in the first step. Specifically, for example, a plurality of fluororesin tapes having drip-proofing properties (liquid-tightness) each of which is with a thickness of 130 μm are prepared as the sheet members 34. Considering that a thickness may be increased by about 10 μm due to an influence of bubbles, when the plurality of fluororesin tapes are adhered to the glass substrates 31 and 32, a thickness of the gap 30 between the glass substrates 31 and 32 can be adjusted to 140×n (μm) by stacking n sheets of fluororesin tapes. Furthermore, the thickness of the gap 30 can also be adjusted to an arbitrary thickness using a fluororesin tape having a thickness other than 130 μm. Since four sheets of sheet members 34 are used in the example shown in
When the thickness of the gap 30 is adjusted, the second liquid L2 containing the oil droplets D prepared in the first step is suctioned by a holding tool 35 such as a syringe and injected from the lower glass substrate 32 exposed upward into the gap 30. The second liquid L2 containing the oil droplets D is smoothly injected into the gap 30 using the capillary phenomenon.
Also in the second step, since a specific gravity of the oil droplets D (first liquid L1) is larger than a specific gravity of the second liquid L2, it is possible to prevent the oil droplets D injected into the gap 30 from floating with respect to the second liquid L2 and localizing upward in a thickness direction of the device DV.
(Third Step)
In a third step, irradiation with ultraviolet light as curing light is performed from outside of the glass substrates 31 and 32 through each of the glass substrates 31 and 32, for example, for 30 minutes. Thus, the second liquid L2 is cured by the irradiation of ultraviolet light UV and the base 20 made of a polyacrylamide that is an external phase is formed as a cured product containing the surfactant and the stabilizer is formed.
(Fourth Step)
Next, a fourth step will be described. In the fourth step, the oil droplets D remaining in the base 20 are removed to form the hole sections 10. The device DV in which the second liquid L2 is cured in the third step and the base 20 is formed is dried at 90° C. for several hours and then immersed in acetone to be cleaned. Thus, the oil droplets D are removed as shown in
Here, in the second step, there is no second liquid L2 or there is a minute amount of second liquid L2 at a portion at which the oil droplets D injected into the gap between the glass substrates 31 and 32 are in contact with each other or a portion at which a distance between neighboring oil droplets D is the shortest. Thus, in the third step, these portions do not have the base 20 formed by curing the second liquid L2 or have a very small thickness. For this reason, through the cleaning in the fourth step, these portions do not have the base 20 formed therein and the neighboring hole sections communicate with each other via the communication holes 11.
When the above-described cleaning is performed by, for example, ultrasonic cleaning (about one hour), the device DV is divided at a central portion at which the communication holes 11 are formed and which has low strength in a thickness direction as shown in
(a) of
Note that, when the porous films 1, 1A, and 1B are separated from the glass substrates 31 and 32, the device DV may be immersed alternately in cold water and hot water.
In the present embodiment, as described above, by using oil droplets D having a desired diameter and a photosetting second liquid L2, a porous film having a hole diameter with a small variation of about 10 μm or more and 2000 μm or less can be manufactured at low cost. Furthermore, in the present embodiment, by selecting the first capillary device 40 or the second capillary device 50 and appropriately selecting the diameter of the nozzle 42, the diameter of the opening 49, and the flow rate of the first liquid L1 in the first step, an arbitrary hole diameter of 10 μm or more and 2000 μm or less can be easily selected and formed.
Also, since the specific gravity of the first liquid L1 is larger than the specific gravity of the second liquid L2 in the present embodiment, porous films 1, 1A, and 1B in which a relative error between particle diameters is small and hole sections 10 are arranged in a uniform distribution can be prepared without a problem such that the oil droplets D (first liquid L1) float with respect to the second liquid L2 and thus the spherical oil droplets D cannot be stably formed and the hole sections 10 are localized upward in a case in which the specific gravity of the first liquid L1 is smaller than the specific gravity of the second liquid L2.
Also, it is conceivable that for example, a gaseous phase such as bubbles may be used instead of a liquid phase when hole sections 10 are formed, but in this case, as described above, since a specific gravity of a gas is smaller than a specific gravity of a second liquid L2, there is concern that there may be a problem such as the hole sections not being able to be stably formed or a problem of the hole sections 10 being arranged in a localized distribution. On the other hand, since the hole sections 10 are formed using the oil droplets D that are a liquid phase in the present embodiment, the specific gravity is easily adjusted as compared with the case of the gaseous phase, and porous films 1, 1A, and 1B in which a relative error between particle diameters is small, and hole sections 10 are arranged in a uniform distribution can be easily prepared.
It is also conceivable to use, for example, a solid phase instead of a liquid phase when hole sections 10 are formed. However, when spherical bodies to be arranged have a solid phase, the spherical bodies are rigid and when the spherical bodies are aggregated at arbitrary positions, there is no flexibility to rearrange these. For this reason, a problem that the hole sections 10 may not be able to be arranged uniformly is concerned.
Note that, when the hole diameter of the hole sections 10 is set to a value different from the average particle diameter shown in
(Second Embodiment of Porous Film)
Next, a porous film according to a second embodiment will be described below with reference to
When the oil droplets D are arranged in the body-centered cubic structure, a height of the two layers (thickness of a gap 30) is represented by the following Expression (1) if radii of the oil droplets D are assumed to be r.
[Math. 1]
(2+√{square root over (2)})r (1)
Also, when the oil droplets D are arranged in the closed-packed structure, a height of the two layers (thickness of a gap 30) is represented by the following Expression (2) if radii of the oil droplets D are assumed to be r.
Therefore, in the case in which the oil droplets D have a two-layer structure, in the above second step, the diameter of the hole sections 10 and the thickness of the gap between the glass substrates 31 and 32 are adjusted to a thickness calculated by Expression (1) or Expression (2) depending on the structure. For example, if the radii of the hole sections 10 (droplets D) are 200 μm (diameter: 400 μm), in the case of the body-centered cubic structure, the thickness of the gap 30 is adjusted to 682 μm, and in the case of the closed-packed structure, the thickness of the gap 30 is adjusted to 726 μm. When the oil droplets D and the second liquid L1 are injected into the gap 30 whose thickness has been adjusted in the second step, the oil droplets D are arranged three-dimensionally in the body-centered cubic structure or the closed-packed structure in accordance with the thickness of the gap 30.
After that, when the above processes of the third step and the fourth step are sequentially performed, a porous film in which hole sections 10 with a small variation of a hole diameter are arranged in the body-centered cubic structure or the closed-packed structure can be manufactured.
If a porous film with a structure in which a plurality of layers of hole sections 10 are arranged is manufactured in this way, it is extremely difficult to perform manufacturing by switching between a body-centered cubic structure and a closed-packed structure when the hole sections 10 are formed in the gaseous phase as described above, but if the hole sections 10 are formed in a liquid phase like in the present embodiment, it is possible to perform manufacturing by easily switching between the body-centered cubic structure and the closed-packed structure in accordance with the thickness of the gap 30.
A constitution in which the hole sections 10 are arranged in two layers is exemplified in the second embodiment, but when the thickness of the gap 30 is set to a value depending on the body-centered cubic structure or the hexagonal close-packed structure, a porous film in which the hole sections 10 are formed in the body-centered cubic structure or the hexagonal close-packed structure over three layers or more can be manufactured.
(Third Embodiment of Porous Film)
A porous film according to a third embodiment will be described below with reference to
When the oil droplets D (D1 to D3) are arranged in the body-centered cubic structure, a height of the three layers (thickness of the gap 30) is represented by the following Expression (3) if radii of the oil droplets D (D1 to D3) are assumed to be r.
[Math. 3]
2(1+√{square root over (2)})r (3)
When the oil droplets D (D1 to D3) are arranged in the face-centered cubic structure, a height of the three layers (a thickness of a gap 30) is represented by the following Expression (4) if radii of the oil droplets D (D1 to D3) are assumed to be r.
Thus, if the oil droplets D have a three layer structure, when a thickness of the gap 30 between the glass substrates 31 and 32 is adjusted to a thickness calculated by Expression (3) or (4) depending on a diameter of the hole sections 10 and their structure in the above second step, a porous film in which the three layers of hole sections 10 are arranged in the body-centered cubic structure or the face-centered cubic structure can be manufactured at low cost.
(Other Embodiments of Porous Film)
Although cases in which the diameters of the oil droplets D and the hole sections are the same have been described in the above-described embodiments, when a plurality of types of oil droplets D with different diameters are prepared in the first step, a porous film 1 (or porous film 1A or 1B) having a plurality of types of hole sections 10 with different diameters can also be manufactured. A plurality of types of oil droplets D with different diameters can be prepared by, for example, selecting the above-described first capillary device 40 or second capillary device 50 and changing at least one of a diameter of the nozzle 42, a diameter of the opening 49, and a flow rate of the first liquid L1. Particularly, a plurality of types of oil droplets D with different diameters can be continuously formed by selecting a method of changing a flow rate of the first liquid L1.
(Application Example of Porous Film)
An application example of the above porous film will be described below.
A porous film 1 according to the present embodiment can be applied to a microlens array.
It is expected that a microlens array will be able to be applied to control of optical properties such as light flux, polarization of light, and a wavelength or preparation of a three-dimensional stereoscopic image by interference of lights from a large number of lens bodies of a microlens array in which micro lenses are arranged regularly. The porous film 1 according to the present embodiment functions as a microlens array when lens bodies are arranged in hole sections 10. Examples of the lens bodies can include a cholesteric liquid crystal microcapsule which is an omni-directional laser oscillator.
A cholesteric liquid crystal is one of liquid crystal materials and has a feature, i.e., “bistability” which means that it can be stable in a state in which it transmits light (focal conic state) and a state in which it reflects light (planar state) without applying electric power. A cholesteric liquid crystal is prepared by adding an additive called a chiral agent to a nematic liquid crystal so as to have optical rotary power. Furthermore, a cholesteric liquid crystal is referred to as a chiral nematic liquid crystal (CN liquid crystal) in some cases. Since a cholesteric liquid crystal has memory characteristics, a display does not disappear even if electric power is turned off, low electric power consumption becomes possible, and the cholesteric liquid crystal can be applied to electronic paper display technology.
As shown in
The porous film 1 according to the present embodiment can be applied to a microreactor.
A microreactor uses a microspace as a reaction field, and in the porous film 1 according to the present embodiment, each of the hole sections 10 functions as a reaction field. Application of a microreactor to a heterogeneous catalytic reaction can be conceived because a specific surface area per volume of the microreactor is large. For this reason, the porous film 1 functions as a microreactor by carrying a catalyst on the porous film 1.
In addition, the reaction in the reaction field can be controlled by controlling a lattice structure or a micro hole diameter of the porous film 1. Since the above-described porous film 1 is provided in the present embodiment, a microreactor having a reaction field of about 10 μm or more and 2000 μm or less can be manufactured at low cost.
The porous film 1 according to the present embodiment can be applied to a bio-device.
Examples of the bio-device include devices serving as scaffolds for cell patterning and devices serving as scaffolds for growth of cell or the like. In order to use cell patterning as, for example, a bio-sensor, it is necessary to control a position at which a cell culture is performed. Cell patterning can be realized by preparing the porous film 1 according to the present embodiment using substances which are not adherent to cells or subjecting the porous film 1 to surface treatment with substances which are not adherent to cells, adhering the porous film 1 on a substrate on which cells are to be cultured, adhering cells on the substrate, and separating the porous film 1. Since this cell patterning uses the porous film 1 according to the present embodiment, a patterning operation of a top-down substrate can be shortened and significant cost reduction can be achieved.
Many conventional porous films are two-dimensional films and two-dimensional growth in cell growth or blood vessel growth has been researched, but when neurospheres are attached to a surface of the porous film 1 using the porous film 1 according to the present embodiment in which the hole sections 10 are formed three-dimensionally and a growth process is observed, three-dimensional growth regarded to be indispensible when application thereof to an actual brain or a human body is considered can be researched at low cost. In addition, different growth processes in the porous film 1 with different lattice structures can also be observed, which can contribute to basic research.
The porous film 1 according to the present embodiment can be applied to a template.
In the porous film 1, the base 20 serves as a mold and a material disposed in each of the hole sections 10 can be molded as a template. In this case, the number of the oil droplets D injected into the gaps 30 between the glass substrates 31 and 32 in the second step may be set not to be dense. With such a constitution, neighboring hole sections 10 can be formed independently without communicating with each other and hole sections 10 in which only portions thereof in contact with the glass substrates 31 and 32 are open can be formed.
While preferred embodiments associated with the present invention have been described above with reference to the accompanying drawings, it goes without saying that the present invention is not limited to these examples. The forms, combinations, or the like of the constituent elements shown in the above-described examples are merely examples and various modifications are possible based on design requirements or the like without departing from the gist of the present invention.
For example, examples of a constitution in which the first liquid L1 is the oil phase and the second liquid L2 is the aqueous phase have been provided in the above embodiments, but the present invention is not limited thereto and a constitution in which the first liquid L1 is an aqueous phase and the second liquid L2 is an oil phase may be provided. In this case, examples of the first liquid L1 which is the aqueous phase include deionized water and examples of the second liquid L2 which is the oil phase can include styrene monomers (84.2% by weight), divinylbenzene (9.8% by weight; a crosslinking agent), PLURONIC P123 (registered trademark) (1.1% by weight; a surfactant), and IRGACURE (registered trademark) TPO (4.9% by weight; a photopolymerization initiator).
An example of a method for manufacturing a porous film using thermal polymerization when the first liquid L1 is an aqueous phase and the second liquid L2 is an oil phase will be shown.
1) A solution was degassed for one hour in the above first step and then purged with nitrogen by bubbling for one hour to prepare a W/O type emulsion. At this time, the composition of the oil phase was 0.92% by weight of a surfactant P123, 84.57% by weight of a styrene monomer (from which a polymerization inhibitor had been removed), 8.66% by weight of divinylbenzene (from which a polymerization inhibitor had been removed), and 5.84% by weight of a thermal polymerization initiator AIBN, and the aqueous phase was deionized water.
2) A porous film was formed by curing at room temperature using the above W/O type emulsion.
3) In order to minimize volatilization of the styrene monomer, a glass cell having the W/O type emulsion sealed therein was put in what is filled with the styrene monomers and was left to stand at room temperature.
By adopting such a method, a porous film can be manufactured by thermal polymerization.
An example of a method for manufacturing a porous film through photopolymerization when the first liquid L1 is an aqueous phase and the second liquid L2 is an oil phase will be shown below.
1) In the same manner as described above, a W/O type emulsion was prepared in the first step. At this time, the oil phase had a composition of 1.40% by weight of a surfactant P123, 77.74% by weight of toluene, and 20.85% by weight of an acrylic curable resin (UNISOLAR (registered trademark), manufactured by Unitec Co., Ltd) and the aqueous phase was deionized water.
2) A porous film was formed by curing the above-described W/O type emulsion through irradiation with ultraviolet light UV.
By adopting such a method, a porous film can be manufactured by photopolymerization.
Although an exemplary example of a constitution in which the second liquid L is cured by imparting light energy to the second liquid L has been provided in the above embodiments, the present invention is not limited thereto. In addition, a constitution in which the second liquid L includes an initiator for curing the second liquid L when thermal energy is imparted, and the base 20 is formed by applying the thermal energy to the second liquid L in the third step so as to cure the second liquid L may be adopted.
As a method for forming the base 20, a constitution in which the base 20 is formed by using a curing agent which cures due to change in pH instead of the curing agent which cures by imparting light energy or thermal energy and curing the second liquid L by changing a pH of the second liquid L may be adopted i.
To be specific, the second liquid L can be cured using a redox initiator such as ammonium persulfate, hydrogen peroxide, and diisopropylpercarbonate as a curing agent which cures due to change in pH and tetraethylenediamine, triethylamine, triethanolamine, or the like as a material changing a pH of the second liquid L.
Although a case in which the hole diameter of the hole sections 10 is a predetermined diameter of 10 μm or more and 2000 μm or less has been exemplified in the above-described embodiments, in order to more stably form the hole sections 10, it is desirable that a hole diameter of the hole sections 10 be 250 μm or more and 2000 μm or less.
Although a constitution in which the plurality of hole sections 10 are arranged in a body-centered cubic structure or a hexagonal close-packed structure has been described in the above-described embodiments, a porous film in which the hole sections 10 are arranged in a face-centered cubic structure can be manufactured in accordance with the present invention in addition to these.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2015-243016 | Dec 2015 | JP | national |
| 2016-142659 | Jul 2016 | JP | national |
The present application is a divisional of U.S. application Ser. No. 16/061,225 filed on Jun. 11, 2018, pending, which is a national stage of PCT/JP2016/086905 filed Dec. 12, 2016 and claims the benefit of Japanese Patent Application Nos. 2015-243016 and 2016-142659, filed Dec. 14, 2015 and Jul. 20, 2016, respectively, the contents of which is incorporated herein by reference.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 16061225 | Jun 2018 | US |
| Child | 18186378 | US |
