Patent Application
20200288652
This application is based on and claims priority under 35 USC 119 from Japanese Patent Application No. 2019-048831 filed Mar. 15, 2019.
The present invention relates to a medium for water culture and water culture apparatus.
Conventionally, water culture for producing plants such as vegetables, fruits, and flowers has been performed. In the water culture, in order to inhibit the growth of pathogens and the like in the culture solution, water purification is performed.
For example, JP2004-082095A discloses “a method and an apparatus for treating an agricultural liquid, in which a purification treatment is performed on an agricultural liquid by using a photocatalyst support and using only sunlight as light for causing a photoreaction of a photocatalyst, and in the photocatalyst support, as a photocatalyst, a microporous film is formed by firing a film that is obtained by coating a porous substrate with a metal alkoxide-containing photoreactive semiconductor and drying and coagulating the semiconductor”.
JP2004-337836A discloses “a photocatalytic substance which includes a photocatalyst layer capable of reacting with sunlight on a surface of a porous substrate, has a porosity that enables light to permeate into the interior of the photocatalytic substance in a thickness direction, and has a shape that can be extended in the form of a plane”. JP2004-337836A also discloses the use of the photocatalytic substance for an agricultural liquid.
JP2011-172539A discloses “a culture apparatus that sterilizes a culture solution for the water culture of plants by irradiating the culture solution with light having a wavelength equal to or shorter than 400 nm in a photoscreened tank in which the wall surface thereof is coated with a photocatalyst”.
WO15/059752A discloses “a water culture apparatus using glass beads supporting a photocatalyst as a medium of a water culture system, in which the adhesion of infectious microbes to the medium is prevented by irradiating a photocatalyst supporting portion with ultraviolet rays”.
JP2014-226108A discloses “a liquid purification apparatus including a light source, a light scattering device, and a photocatalytic substance disposed around the light scattering device, in which the photocatalytic substance is supported on a support and immersed in a liquid medium.”
JP2006-238717A discloses “a culture medium housing tool in which a titanium oxide film is formed whose surface is doped with carbon in the form of a Ti—C bond by a heating treatment performed on a titanium plate at a high temperature”.
JP2007-089425A discloses “an apparatus for purifying a liquid for plant cultivation that purifies a liquid for plant cultivation by adding an apatite-containing photocatalyst to the liquid for plant cultivation and circulating the photocatalyst”.
JP2010-094026A discloses “a water storage apparatus in which water is purified by filling a water storage tank for cultivation with glass beads coated with a visible light-type photocatalyst and circulating water”.
JP2006-320282A discloses “a sterilization apparatus for circulating and supplying a culture solution, including a treatment tank which is for performing a sterilization treatment on an excess of a culture solution supplied to a culture bed from a culture solution tank and a sterilization member (non-woven cloth containing chelated silver ions) which contains an antibacterial active metal compound constituting a photocatalyst capable of performing a sterilizing action by light irradiation, in which the excess of the culture solution is circulated between the treatment tank and the sterilization apparatus such that the excess of the culture solution is sterilized”.
JP1998-249210A (Alias: JP10-249210A) discloses “a method for sterilizing a culture solution for water culture, including passing a culture solution through a photocatalytic substance having a specific gravity adjusted for the photocatalytic substance to float on and/or sink in water and radiating light including ultraviolet rays, in which the photocatalytic substance is obtained by fixing photocatalyst particles to the surface of hollow glass particle substrates by using an inorganic substance as a binder”.
JP2012-006003A discloses “a water treatment method in which photocatalyst-supporting recycled foamed glass, which is obtained by causing a photocatalyst to be supported on recycled foamed glass having a specific gravity smaller than that of water, is caused to float on water to be treated such that organic substances or bacteria in the water to be treated are efficiently decomposed, sterilized, and removed by sunlight”.
Aspects of non-limiting embodiments of the present disclosure relate to a medium for water culture that sterilizes and purifies a culture solution while further inhibiting the inactivation of culture components in the culture solution, compared to a medium for water culture including a porous substance and photocatalyst particles supported on the porous substance and formed of titanium-based compound particles having absorption only in the range of ultraviolet.
Aspects of certain non-limiting embodiments of the present disclosure address the features discussed above and/or other features not described above. However, aspects of the non-limiting embodiments are not required to address the above features, and aspects of the non-limiting embodiments of the present disclosure may not address features described above.
According to an aspect of the present disclosure, there is provided a medium for water culture including a porous substance and photocatalyst particles formed of titanium-based compound particles that are supported on the porous substance, have absorption at a wavelength of 500 nm in a visible absorption spectrum, and have an absorption at 2,700 cm−1 to 3,000 cm−1 in an infrared absorption spectrum, in which a metal compound having a metal atom and a hydrocarbon group is bonded to the surface of each of the titanium-based compound particles through an oxygen atom.
Exemplary embodiment(s) of the present invention will be described in detail based on the following figures, wherein:
Hereinafter, embodiments as an example of the present invention will be described.
In the present specification, in a case where the amount of each component in a composition is mentioned, and there is a plurality of kinds of substances in the composition that correspond to each component, unless otherwise specified, the amount means the total amount of the plurality of kinds of substances present in the composition.
The term “step” includes not only an independent step but also a step which cannot be clearly differentiated from other steps, as long as the intended goal of the step is accomplished.
“XPS” is an abbreviation of X-ray Photoelectron Spectroscopy.
(Medium for Water Culture)
A medium for water culture according to the present embodiment includes a porous substance and photocatalyst particles supported on the porous substance.
The photocatalyst particles are formed of titanium-based compound particles (hereinafter, referred to as “specific titanium-based compound particles” as well) have absorption at a wavelength of 500 nm in a visible absorption spectrum and have an absorption peak at 2,700 cm−1 to 3,000 cm−1 in an infrared absorption spectrum, in which a metal compound having a metal atom and a hydrocarbon group is bonded to the surface of each of the titanium-based compound particles through an oxygen atom.
“Specific titanium-based compound particles” as the photocatalyst particles have absorption at a wavelength of 500 nm in a visible absorption spectrum and have an absorption peak at 2, 700 cm−1 to 3,000 cm−1 in an infrared absorption spectrum, and express a photocatalytic ability in the range of visible light, in which a metal compound having a metal atom and a hydrocarbon group is bonded to the surface of each of the titanium-based compound particles through an oxygen atom.
Owing to the above constitution, the medium for water culture according to the present embodiment sterilizes and purifies a culture solution while inhibiting the inactivation of culture components in the culture solution.
The reason is assumed to be as below.
First, in recent years, due to the aging of people engaged in agriculture and the reduction of the number of people engaged in agriculture, there has been an increasing expectation on a plant factory which can stably produce high-quality and inexpensive plants (for example, foods (vegetables, fruits, and the like) and ornamental plants (flowers and the like)) in a planned way.
The plant factory is roughly classified into “sunlight utilization-type” facilities and “fully controlled” facilities.
“Sunlight utilization-type” facilities use sunlight in a semi-closed environment such as a glass greenhouse or a vinyl greenhouse so as to supplement lighting in rainy days or cloudy days and inhibit temperature increase in summer.
“Fully controlled” facilities use artificial light from a light source such as Light Emitting Diode (LED) in an indoor environment such as a building and are controlled in terms of environmental factors such as temperature and humidity.
In any of the facilities, water culture by which plants grow in a culture solution without using soil is generally performed. By the water culture, plants are cultivated in a culture solution without using soil. Therefore, the water culture less causes a failure resulting from repeated cultivation. Furthermore, in the water culture, temperature and humidity, light, nutrients, carbon dioxide, and the like are controlled. Therefore, the environment optimal for the growing plants is maintained, and a growth rate is increased.
Accordingly, the water culture has an advantage of being capable of stably harvesting and shipping in a planned way within a short period of time without being influenced by weather.
In the water culture, a culture solution is used. Therefore, in a case where pathogens occur in the culture solution, the pathogens move to plants through the culture solution. Therefore, the interior of facilities, a water culture apparatus, agricultural tools, materials, and the like are washed and sterilized. In addition, restriction on people's entry to the facilities, hand washing, change of clothes, and the like are pursued.
Therefore, the management for keeping the culture solution sterile is complicated, and the management cost tends to increase.
As a method for inhibiting the occurrence of pathogens in the culture solution (that is, a method for sterilizing and purifying the culture solution), there is a method of adding a drug (chlorine agent or the like) to the culture solution or a method of heat-sterilizing the culture apparatus, the agricultural materials, the culture solution, and the like.
However, it is apprehended that the drug (chlorine agent or the like) may damage the root of plants. Furthermore, because the heat sterilization requires huge amounts of energy, the culture costs increase.
As the method for inhibiting the occurrence of pathogens in the culture solution (that is, a method for sterilizing and purifying the culture solution), there are also a method of sterilizing and purifying the culture solution by using a photocatalyst exploiting ultraviolet light or infrared light and a method of sterilizing and purifying the culture solution by using photocatalyst exploiting visible light.
In the sterilization and purification of the culture solution by using a photocatalyst exploiting ultraviolet light or infrared light, due to the strong oxidative action, not only the sterilization and purification but also the insolubilization of organic substances or ions in a liquid is accelerated. As a result, in the water culture, sometimes the culture components (for example, organic substances obtained by the chelation of iron, manganese, copper, zinc, and the like (that is, metal chelate compounds), ions of iron, manganese, copper, and zinc, and the like) in the culture solution are insolubilized and inactivated.
The sterilization and purification of the culture solution using a photocatalyst exploiting visible light are performed using a film containing the photocatalyst. Therefore, it is difficult to sterilize and purify the culture solution. With the low sterilization and purification efficiency of the culture solution, in a case where the culture solution is not circulated, the replacement of culture solution that is a cumbersome operation needs to be performed, and in a case where the culture solution is circulated, a circulation rate of the culture solution needs to be reduced. Therefore, it is difficult for the plants to grow.
As described above, for the sterilization and purification of the culture solution, water culture is required which makes it possible to sterilize and purify the culture solution while inhibiting the inactivation of culture components in the culture solution.
The medium for water culture according to the present embodiment is constituted with a porous substance supporting “specific titanium-based compound particles” as photocatalyst particles.
Each of “specific titanium-based compound particles” as photocatalyst particles has a structure in which a metal compound having a metal atom and a hydrocarbon group is bonded to the surface of each of the titanium-based compound particles through an oxygen atom, and has a high specific surface area. Therefore, these particles exhibit high adsorptivity to germs. Furthermore, these particles are hardly aggregated and have high dispersibility.
The specific titanium-based compound particles have absorption at a wavelength of 500 nm in a visible absorption spectrum and perform a high photocatalytic function in the range of visible light. The wavelength range around a wavelength of 500 nm in a visible absorption spectrum is the wavelength range of reflected light from leaves of plants and the like (specifically, green reflected light). Therefore, the specific titanium-based compound particles express a photocatalytic function by exploiting the reflected light from the leaves of plants and the like.
The photocatalyst particles, which have the dispersibility and the absorptivity described above and exhibit a high photocatalytic function in the range of visible light, are supported on the porous substance substantially in a uniform state, and express high germ adsorptivity and a high photocatalytic function in the range of visible light.
However, the oxidative action of “specific titanium-based compound particles” as photocatalyst particles is milder than the oxidative action of a photocatalyst exploiting ultraviolet light or infrared light. Therefore, while the sterilization and purification are promoted, the insolubilization of the culture components in the culture solution is inhibited.
Presumably, for the above reason, the medium for water culture according to the present embodiment may sterilize and purify the culture solution while inhibiting the inactivation of the culture components in the culture solution.
Accordingly, with a water culture apparatus including the medium for water culture according to the present embodiment, even though the culture solution is not circulated, the number of times the culture solution is replaced is reduced, and even though the culture solution is circulated, by increasing the circulation rate of the culture solution, plants grow. In addition, the culture solution is sterilized and purified using a photocatalyst which exploits visible light having weaker oxidative action compared to a photocatalyst exploiting ultraviolet light or infrared light. Therefore, the damage of the root of the plants is inhibited. This point also favors the growth of plants.
In order to sterilize and purify the culture solution by using a photocatalyst exploiting ultraviolet light or infrared light, expensive facilities and large facilities are required. In contrast, in the sterilization and purification of the culture solution by using the medium for water culture according to the present embodiment, the sterilization and purification can be performed using sunlight as well as reflected light from an object (for example, reflected light from leaves of plants and the like) including visible light.
That is, even though the culture solution is sterilized and purified in an indoor environment such as a building by using the water culture apparatus including the medium for water culture according to the present embodiment, it is possible to use a light source such as a general-purpose LED radiating light of a visible range. Therefore, the water culture apparatus including the medium for water culture according to the present embodiment is advantageous in terms of cost reduction of facilities and downsizing of facilities.
Hereinafter, the present embodiment will be specifically described with reference to drawings. In some cases, the members substantially having the same function are marked with the same references throughout all the drawings so as to avoid the redundancy of description.
(Water Culture Apparatus)
As shown in
The water culture apparatus 101 is, for example, a Nutrient Film Technique-type water culture apparatus (that is, an NFT-type water culture apparatus). The water culture apparatus 101 may also be a Deep Flow Technique-type water culture apparatus (that is, a DFT-type water culture apparatus).
In the water culture apparatus 101, the circulation device 50 and the light irradiation device 60 are provided as necessary.
—Culture Solution—
Examples of the culture solution include an aqueous solution containing nutrients for the plant 12. Examples of the nutrients for the plant 12 include nutrients containing nitrogen, phosphorus, potassium, calcium, magnesium, sulfur, boron, iron, manganese, zinc, molybdenum, and the like. The nutrients for the plant 12 include inorganic nutrients and organic nutrients containing the elements described above.
The composition of the nutrients for the plant 12 in the culture solution is selected according to the plant 12 to grow and the growing condition of the plant 12.
Examples of the inorganic nutrients include known nutrients such as potassium nitrate, calcium nitrate, sodium nitrate, urea, ammonium sulfate, ammonium chloride, ammonium phosphate, potassium phosphate, potassium chloride, potassium sulfate, calcium phosphate, calcium chloride, magnesium sulfate, ferrous sulfate, iron (ii) sulfide, boric acid, sodium borate, manganese sulfate, manganese chloride, zinc sulfate, zinc chloride, copper sulfate, ammonium molybdate, and sodium molybdate.
Examples of the organic nutrients include known nutrients such as organic substances (that is, metal chelate compounds) obtained by chelating iron, manganese, copper, zinc, and the like. Examples of chelating agents include ethylenediaminetetraacetic acid (EDTA), diethylenetriamine-N,N,N′,N″, N″-pentaacetic acid (DTPA), and ethylenediamine-di(o-hydroxyphenylacetic acid) (EDDHA).
Particularly, the water culture apparatus 101 inhibits the insolubilization of nutritional components in the culture solution and inhibits the inactivation of nutrients. Therefore, even though the culture solution particularly contains nutrients (for example, organic nutrients obtained by chelating iron, manganese, copper, zinc, and the like (that is, metal chelate compounds) and inorganic nutrients including iron, manganese, copper, zinc, and the like) that are easily insolubilized by the action of a photocatalyst exploiting ultraviolet light or infrared light, the water culture apparatus 101 has an advantage of inhibiting the insolubilization of these nutrients.
—Container—
Container 20
In the water culture apparatus 101, the container 20 is, for example, a tank in the form of an open-top box.
The bottom portion of the container 20 is connected to a discharge pipe 56 of a circulation device 50. The discharge pipe 56 of the circulation device 50 may be connected to a lateral wall portion of the container 20.
The container 20 is constituted, for example, with one tank. The container 20 may be constituted with a plurality of tanks.
—Medium Member—
The medium member 30 is, for example, a plate-shaped member supporting the root of the plant 12 to grow. The medium member 30 may be a member which holds the entirety or a portion of the root of the plant 12, or a member which does not hold the root of the plant 12. The shape of the medium member 30 is not particularly limited, and may be, for example, a cubical shape.
The medium member 30 is disposed such that the root of the plant 12 to grow contacts the culture solution 14 in the container 20. Specifically, the medium member 30 is disposed to contact the culture solution 14 in the container 20.
The medium member 30 has, for example, a supporting portion 32 supporting the plant 12 and a holding portion 34 holding the supporting portion 32.
The supporting portion 32 and the holding portion 34 are constituted as, for example, separate substances (see
The supporting portion 32 is, for example, a member of a cylindrical portion having a hole for supporting the plant 12 by allowing the plant 12 to be inserted into the hole. The shape of the supporting portion 32 is not particularly limited. For example, the supporting portion 32 may be a sheet-shaped member supporting the plant 12 by wrapping the plant.
The supporting portion 32 and the holding portion 34 may be constituted as an integrated substance (see
In the medium member 30, at least one of the supporting portion 32 or the holding portion 34 is constituted with a medium for water culture which will be described later.
The medium for water culture may be positioned at the site where the medium member 30 contacts (for example, immersed in) the culture solution.
—Circulation Device—
The circulation device 50 has, for example, a storage tank 52 storing the culture solution 14, a supply pipe 54 supplying the culture solution 14 in the storage tank 52 to the container 20, and the discharge pipe 56 discharging the culture solution 14 in the container 20 to the storage tank 52.
For example, one end of the supply pipe 54 is connected to the storage tank 52, and the other end thereof is disposed in a position where the culture solution 14 can be supplied to the container 20 (for example, the position above one end portion of the container 20). In the middle of the route of the supply pipe 54, for example, a pump and a valve are disposed although these are not shown in the drawing.
For example, one end of the discharge pipe 56 is connected to the storage tank 52, and the other end thereof is disposed in a position where the culture solution 14 in the container 20 can be discharged (for example, the bottom portion or the lateral wall portion of the container 20 that is on the side opposite to the position in which the other end of the supply pipe 54 is disposed). In the middle of the route of the supply pipe 56, for example, a pump and a valve are disposed although these are not shown in the drawing.
From the viewpoint of sterilizing and purifying the culture solution, a calculative flow rate of the culture solution 14 flowing in the medium for water culture, which will be described later, that is calculated from an amount of the culture solution 14 supplied to the container 20 per unit time by the circulation device 50 (L/min (Liter/minute)) and a contact area between the culture solution and the bottom surface of the container (m2) is, for example, preferably equal to or higher than 0.1 (L/min/m2) and equal to or lower than 50 (L/min/m2), more preferably equal to or higher than 0.5 (L/min/m2) and equal to or lower than 20 (L/min/m2), and even more preferably equal to or higher than 1 L/min/m2 and equal to or lower than 10 L/min/m2.
The calculative flow rate of the culture solution 14 flowing in the medium for water culture is calculated as below.
Flow rate of culture solution flowing in medium for water culture (L/min/m2)=amount of culture solution supplied per unit time (L/min)/contact area between culture solution and bottom surface of container (m2)
In a case where the medium for water culture having the same area as the bottom surface of the container 20 is disposed, and the entirety of the culture solution 14 is irradiated with light, the contact area between the culture solution 14 and the bottom surface of the container 20 can also be defined as an irradiated area of a medium 14 for water culture.
In the present specification, the irradiated area of the medium for water culture is the total area of the medium for water culture exposed to visible light. Specifically, the irradiated area equals an area exposed to visible light and, for example, is the area of the medium for water culture irradiated with visible light from a light source 62 of the light irradiation device 60.
The circulation device 50 is not particularly limited as long as it is a device circulating the culture solution 14 held in the container 20. For example, the circulation device 50 may be a known device adopting a method in which one of the supply and discharge of the culture solution 14 in the container 20 is performed by gravity flow and the other is performed using a liquid supply machine such as a pump.
—Light Irradiation Device—
The light irradiation device 60 is, for example, a device irradiating the plant 12 to grow and the medium for water culture with visible light (for example, a device in which a portion radiating light is disposed in a position above the container 20).
The light irradiation device 60 may be a device irradiating at least the medium for water culture with visible light. In a case where the water culture apparatus 101 is installed in an indoor environment to which sunlight does not reach or does not easily reach, for example, the light irradiation device 60 may be a device irradiating the plant 12 and the medium for water culture with visible light.
The light irradiation device 60 has the light source 62 emitting visible light. Examples of the light source 62 include a Light Emitting Diode (LED) unit, a laser unit, a fluorescent lamp, and the like.
In a case where only the medium for water culture is irradiated with visible light, the light source 62 may be a light source radiating visible light in a wavelength range including “wavelength of 500 nm in a visible absorption spectrum” absorbed by at least the photocatalyst particles (titanium-based compound particles) of the medium for water culture.
In contrast, in a case where the plant 12 is also irradiated with visible light in addition to the medium for water culture, for example, the light source 62 may be a light source radiating visible light in a wavelength range including the entire range of visible light (for example, a wavelength in a range equal to or longer than 360 nm and equal to or shorter than 830 nm).
The light irradiation device 60 is not particularly limited as long as it is a device irradiating at least the medium for water culture with visible light. The light irradiation device 60 may be a known device such as a device which irradiates the medium for water culture with the visible light emitted from the light source 62 through a reflection plate or a light guiding path (optical fiber or the like) or a device which causes diffused reflection of the visible light emitted from the light source 62 and then irradiating the medium for water culture with the light.
The water culture apparatus 101 according to the present embodiment described above includes the medium for water culture as at least one of the supporting portion 32 or the holding portion 34 of the medium member 30. Therefore, the apparatus sterilizes and purifies the culture solution while inhibiting the insolubilization of culture components in the culture solution.
The water culture apparatus 101 according to the present embodiment is not limited to the above constitution, and various known water culture apparatuses may be applied thereto. For example, an apparatus adopting the following method may be applied to the water culture apparatus 101 according to the present embodiment.
1) Apparatus adopting method in which the culture solution 14 is not circulated.
2) Apparatus adopting method in which concentrated solution of culture solution 14 is supplied to culture solution 14 in storage tank 52 of container 20 or circulation device.
3) Apparatus adopting method in which oxygen is supplied to culture solution 14 in container 20 or storage tank 52 of circulation device.
(Medium for Water Culture)
Hereinafter, a medium for water culture, which is applied to at least one of the supporting portion or the holding portion of the medium member of the water culture apparatus according to the present embodiment (hereinafter, referred to as “medium for water culture according to the present embodiment” as well), will be specifically described.
The medium for water culture according to the present embodiment includes a porous substance and photocatalyst particles supported on the porous substance.
—Porous Substance—
The porous substance is a member on which each the photocatalyst particles are to be supported, and may or may not have liquid permeability.
The porous substance may be a member having flexibility or a member having rigidity. That is, the porous substance may or may not have self-supporting properties.
The porous substance (at least the surface of the porous substance) may be hydrophilic or hydrophobic. From the viewpoint of improving the affinity with the culture solution to be purified and making it easy to sterilize and purify the culture solution, for example, it is preferable that the porous substance is hydrophilic.
Hydrophilicity means properties of easily absorbing water and easily wet with water. A degree of hydrophilicity can be represented by a contact angle with respect to water (hereinafter, simply referred to as “water contact angle” in some cases).
In a case where an object is hydrophilic, a contact angle of the surface of the object with respect to water is, for example, preferably equal to or smaller than 90°, more preferably equal to or smaller than 60°, and most preferably equal to or smaller than 30°. In a case where water is added dropwise to the surface of an object to be measured, an angle is formed between the surface and the surface of water. The aforementioned water contact angle means the angle formed as above. The larger the water contact angle, the more difficult it is for the object to be wet with water, and the smaller the water contact angle, the easier it is for the object to be wet with water.
The water contact angle is measured using a goniometer or the like. Specifically, in an environment of 23° C. and 55% RH, water is added dropwise to the surface of an object. At this time, after the object is left as it is for 60 seconds, the contact angle is measured using a contact angle meter CA-X (manufactured by Kyowa Interface Science Co., LTD.).
In a case where water has entered the hole of the porous substance as an object, the contact angle is measured in a state where the water has entered the hole.
The average pore size of the porous substance is within a range equal to or greater than 0.5 μm and equal to or smaller than 100 μm. For example, the average pore size is larger than the particle diameter of the photocatalyst particles.
Specifically, the average pore size of the porous substance is, for example, preferably equal to or greater than 1 μm and equal to or smaller than 50 μm, and more preferably equal to or greater than 1.5 μm and equal to or smaller than 30 μm.
The average pore size of the porous substance is measured as below.
The porous substance is observed and imaged using a scanning electron microscope (manufactured by Hitachi, LTD., S-4100). At this time, the porous substance is imaged by adjusting the magnification such that a plurality of pores of the porous substance can be observed by the scanning electron microscope, and the average pore size is measured.
For example, in a case where the porous substance is constituted with a metal, glass, ceramics, and the like, the pores are elliptical or amorphous. Accordingly, the major axis (that is, the longest diameter) of the pores is adopted as a pore size.
In addition, for example, in a case where the porous substance is constituted with fibrous materials such as paper, non-woven cloth, and cloth, the major axis (that is, the longest diameter) of a hole formed by the interweaving and stacking of fibers is adopted as a pore size.
The pore size is measured as above for 10 to 50 pores, and the average thereof is adopted as the average pore size.
The average pore size of the porous substance means the average pore size of the materials constituting the porous substance.
Examples of the materials constituting the porous substance include a fibrous material, a porous resin substance (a porous resin film (for example, a membrane), sponge, or the like), a porous metallic substance, a porous glass substance, a porous ceramic substance, and the like.
Examples of the fibrous material include cloth, knitting, non-woven cloth, paper, and the like.
Examples of the fiber include natural fiber (cotton, silk, linen, wool, pulp, or the like) and synthetic fiber (nylon fiber, polyester fiber, acryl fiber, polyurethane fiber, polyolefin fiber, cellulose fiber, vinyl alcohol fiber, or the like).
Among these, although there is no particular limitation, fiber to which photocatalyst particles easily adhere is preferable. Specifically, although there is no particular limitation, polyolefin fiber (polyethylene fiber, polypropylene fiber, or the like), polyester fiber (polyester terephthalate fiber or the like), cellulose fiber (cellulose triacetate fiber, cellulose diacetate fiber, or the like), and polyvinyl alcohol fiber (ethylene-vinyl alcohol fiber or the like) are preferable.
As the fiber to which photocatalyst particles easily adhere, there is also core-sheath type composition fiber having a core portion and a sheath portion surrounding the core portion. It is better for the core portion to be constituted with a hydrophobic resin having a high melting point (a polypropylene resin, a polyester resin, a cellulose resin, or the like). It is better for the sheath portion to be constituted with a hydrophilic resin having a low melting point (melting point lower than that of the resin of the core portion) (a polyethylene resin, a polyvinyl alcohol resin (ethylene-vinyl alcohol copolymer resin), or the like).
Examples of the porous resin substance include a porous resin film (for example, a membrane) such as polystyrene (PS), polyvinylidene fluoride (PVDF), polytetrafluoroethylene (PTFE), or polyether sulfone; sponge such as urethane or polypropylene; and the like.
Examples of the paper include various types of paper, including fine paper using 100% virgin paper; recycled paper blended with 100% recycled pulp; paper obtained by mixing these together at any ratio; paper obtained by changing the proportion of an NBKP material or an LBKP material used; paper using a plant fiber material such as kenaf or bamboo other than wood pulp; paper treated by clay coating; and the like. Furthermore, examples of the paper include paper to which a filler such as calcium carbonate is added so as to improve whiteness, opacity, or smoothness and paper to which a resin such as polyacrylamide or epoxy-modified polyamide is added so as to improve flexibility or strength.
Examples of the porous metallic substance include porous metallic substances obtained by sintering a metal or an alloy such as SUS, aluminum, or nickel.
Examples of the porous glass substance include porous glass substances obtained by sintering spherical quartz glass powder.
Examples of the porous ceramic substance and the like include porous ceramic substances obtained by sintering ceramics such as alumina or zirconia.
Among these, from the viewpoint of sterilizing and purifying the culture solution, as the material constituting the porous substance, although there is no particular limitation, the fibrous material is preferable. That is, although there is no particular limitation, it is preferable that the porous substances are constituted with fiber.
Hereinafter, the porous substance constituted with fiber will be referred to as “porous substance made of fiber” as well.
From the viewpoint of liquid permeability, flexibility, rigidity, photocatalyst particle holding properties, and the like, the average diameter of the fiber (that is, the average fiber diameter) constituting the porous substance made of fiber is, for example, preferably equal to or greater than 0.5 μm and equal to or smaller than 100 μm, and more preferably equal to or greater than 1 μm and equal to or smaller than 50 μm.
From the viewpoint of liquid permeability, flexibility, rigidity, photocatalyst particle holding properties, and the like, the average length of the fiber (that is, the average fiber length) constituting the porous substance made of fiber is, for example, preferably equal to or greater than 0.5 mm and equal to or smaller than 5 mm, and more preferably equal to or greater than 0.8 mm and equal to or smaller than 1.8 mm.
The average fiber diameter and the average fiber length of the fiber constituting the porous substance is an arithmetic mean of fiber diameters (here, the fiber diameter is the longest diameter) and fiber lengths of 20 strands of fiber measured through electron microscopy.
From the viewpoint of liquid permeability, flexibility, rigidity, photocatalyst particle holding properties, and the like, the basis weight of the porous substance made of fiber is, for example, preferably equal to or greater than 10 g/m2 and equal to or smaller than 8,000 g/m2, more preferably equal to or greater than 30 g/m2 and equal to or smaller than 6,000 g/m2, and even more preferably equal to or greater than 50 g/m2 and equal to or smaller than 4,000 g/m2.
The basis weight of the porous substance made of fiber is a value measured based on JIS P 8124(2011).
From the viewpoint of sterilizing and purifying the culture solution, the thickness of the porous substances made of fiber is, for example, preferably equal to or greater than 0.05 mm and equal to or smaller than 50 mm, and preferably equal to or greater than 0.1 mm and equal to or smaller than 30 mm.
As the porous substance, a plurality of sheets of porous substances having a visible light transmittance, which will be described later, in a preferred range that are stacked to have a total thickness within the above range may be used.
The shape of the porous substance is not particularly limited, and may be a known shape such as a plate shape, a circular columnar shape, a cylindrical shape, a rectangular columnar shape, or an angulated cylindrical shape.
The shape of the porous substance may have a honeycomb structure formed of the material constituting the porous substance.
—Photocatalyst Particles—
The photocatalyst particles are in the medium for water culture in a state of being supported on the inner wall of the pores of the porous substance (in a case where the porous substance is constituted with fiber, the photocatalyst particles are supported on the fiber) (see
For example, in a case where the photocatalyst particles are metatitanic acid particles or titanium oxide particles, the photocatalyst particles are in the medium for water culture in a state of primary particles or in a state of aggregated particles formed by the aggregation of the primary particles (see
In addition, for example, in a case where the photocatalyst particles are titanium oxide aerogel particles and silica-titania composite aerogel particles, the photocatalyst particles are in the medium for water culture as an aggregate having an aerogel structure (see
In
Hereinafter, the photocatalyst particles will be specifically described. In the following description, references will not be mentioned.
The photocatalyst particles have absorption at a wavelength of 500 nm in a visible absorption spectrum, and have an absorption peak at 2,700 cm−1 to 3,000 cm−1 in an infrared absorption spectrum. Accordingly, the photocatalyst particles exhibit a high catalytic function by visible light.
Specifically, each of the photocatalyst particles is a titanium-based compound particle in which a metal compound having a metal atom and a hydrocarbon group is bonded to the surface of each of the titanium-based compound particles through an oxygen atom.
The particles, in which the metal compound having a metal atom and a hydrocarbon group is bonded to the surface of each of the particles through an oxygen atom, are obtained, for example, by performing a surface treatment on untreated particles (for example, metatitanic acid particles, titanium oxide particles, titanium oxide aerogel particles, and silica-titania composite aerogel particles that are untreated) by using a metal compound having a hydrocarbon group and then oxidating at least a portion of the hydrocarbon group by a heating treatment such that the hydrocarbon group is changed to a C—O bond or a C═O bond. Presumably, because a structure, in which an organic metal compound containing appropriately oxidized carbon atoms, oxygen atoms, and titanium atoms (or silicon atoms) are connected to each other in this order through a covalent bond, is on the surface of the particles, the surface of the particles may exhibit absorptivity at a wavelength of 500 nm, and the particles may express a photocatalytic function by visible light (responsiveness to visible light), although the detailed mechanism thereof is unclear.
Hereinafter, the metal compound having a metal atom and a hydrocarbon group will be simply referred to as “organic metal compound” as well.
The photocatalyst particles also have the following advantages in addition to expressing a high photocatalytic function even in the range of visible light.
Generally, untreated particles (for example, metatitanic acid particles, titanium oxide particles, titanium oxide aerogel particles, and silica-titania composite aerogel particles that are untreated) have high hydrophilicity and are very easily aggregated. Therefore, these particles tend to exhibit poor dispersibility and adhesiveness with respect to the porous substance.
However, in a case where the photocatalyst particles have a hydrocarbon group derived from the organic metal compound on the surface thereof, the hydrophobicity thereof is enhanced, and the dispersibility and the adhesiveness thereof with respect to the porous substance are improved. Consequently, the photocatalyst particles are supported on the surface of the porous substance substantially in a uniform state. Furthermore, the photocatalyst particles are hardly detached from the porous substance.
—Untreated Particles—
Examples of the particles (untreated particles) to be subjected to a surface treatment using an organic metal compound include untreated titanium-based compound particles. Examples of the untreated titanium-based compound particles include untreated particles such as metatitanic acid particles, titanium oxide particles, titanium oxide aerogel particles, and silica-titania composite aerogel particles. Among these, from the viewpoint of improving the adhesiveness with respect to the porous substance, although there is no particular limitation, untreated metatitanic acid particles are preferable.
That is, as the photocatalyst particles, although there is no particular limitation, at least one kind of particles selected from the group consisting of metatitanic acid particles, titanium oxide particles, titanium oxide aerogel particles, and silica-titanium composite aerogel particles are preferable. Although there is no particular limitation, metatitanic acid particles are preferable.
In a case where the photocatalyst particles are caused to adhere to the surface of the porous substance as an aggregate having an aerogel structure, as the untreated titanium-based compound particles, at least one kind of particles between the untreated titanium oxide aerogel particles and the silica-titania composite aerogel particles may be used.
—Untreated Metatitanic Acid Particles—
The untreated metatitanic acid particles refer to particles of titanic acid as one of the titanic acid hydrates represented by TiO2.nH2O in which n=1.
The method for preparing the untreated metatitanic acid particles is not particularly limited, and examples thereof include a chlorine method (gas phase method) and a sulfuric acid method (liquid phase method). Between these, although there is no particular limitation, the sulfuric acid method (liquid phase method) is preferable.
For example, the sulfuric acid method (liquid phase method) is as below. First, as a raw material, ilmenite ore (FeTiO3) or tungsten is dissolved in concentrated sulfuric acid, and an iron component, which is an impurity, is isolated as iron sulfate (FeSO4), thereby preparing titanium oxysulfate (TiOSO4) (titanyl sulfate solution). Then, by hydrolyzing the titanium oxysulfate (TiOSO4), untreated metatitanic acid [titanium oxyhydroxide (TiO(OH)2)] particles are obtained.
From the viewpoint of expressing a high photocatalytic function, a BET specific surface area of the untreated metatitanic acid particles is, for example, preferably equal to or greater than 50 m2/g and equal to or smaller than 300 m2/g, more preferably equal to or greater than 80 m2/g and equal to or smaller than 280 m2/g, and even more preferably equal to or greater than 120 m2/g and equal to or smaller than 250 m2/g. The BET specific surface area of the metatitanic acid particles is determined by a gas adsorption method using a nitrogen gas.
—Untreated Titanium Oxide Particles—
Examples of the untreated titanium oxide particles include particles of titanium oxide of a brookite type, an anatase type, a rutile type, and the like. The titanium oxide particles may have either a single crystal structure such as brookite, anatase, and rutile, or a mixed crystal structure in which these crystals coexist.
The method for preparing the untreated titanium oxide particles is not particularly limited, and examples thereof include a chlorine method (gas phase method) and a sulfuric acid method (liquid phase method).
From the viewpoint of expressing a high photocatalytic function, a BET specific surface area of the untreated titanium oxide particles is, for example, preferably equal to or greater than 20 m2/g and equal to or smaller than 250 m2/g, more preferably equal to or greater than 50 m2/g and equal to or smaller than 200 m2/g, and even more preferably equal to or greater than 80 m2/g and equal to or smaller than 180 m2/g. The BET specific surface area of the titanium oxide particles is determined by a gas adsorption method using a nitrogen gas.
—Untreated Titanium Oxide Aerogel Particles—
It is better that the untreated titanium oxide aerogel particles are manufactured by a sol-gel method using a titanium alkoxide as a material.
Although there is no particular limitation, it is preferable that the untreated titanium oxide aerogel particles are formed of a hydrolysis condensate of a titanium alkoxide. Here, a portion of the alkoxy group in the titanium alkoxide may remain in the particles in an unreacted state.
From the viewpoint of expressing a high photocatalytic function, a BET specific surface area of the untreated titanium oxide aerogel particles is, for example, preferably equal to or greater than 120 m2/g and equal to or smaller than 1,000 m2/g, more preferably equal to or greater than 150 m2/g and equal to or smaller than 900 m2/g, and even more preferably equal to or greater than 180 m2/g and equal to or smaller than 800 m2/g. The BET specific surface area of the untreated titanium oxide aerogel particles is determined by a gas adsorption method using a nitrogen gas.
Hereinafter, a manufacturing method of the untreated titanium oxide aerogel particles will be described.
For example, it is preferable that the manufacturing method of the untreated titanium oxide aerogel particles includes at least the following (1) and (2).
(1) Making porous particles containing titanium oxide by sol-gel method and preparing dispersion liquid containing the porous particles and solvent (preparation of dispersion liquid)
(2) Removing the solvent from the dispersion liquid by using supercritical carbon dioxide (removal of solvent)
(1) Preparation of Dispersion Liquid
In the preparation of a dispersion liquid, for example, by using a titanium alkoxide as a material, titanium oxide is generated by causing reactions (hydrolysis and condensation) of the titanium alkoxide, thereby obtaining a dispersion liquid in which titanium oxide-containing porous particles are dispersed in a solvent.
Specifically, the preparation of a dispersion liquid is performed as below.
A titanium alkoxide is added to an alcohol and stirred, and in this state, an aqueous solution of an acid is added dropwise thereto such that the titanium alkoxide reacts and generates titanium oxide, thereby obtaining a dispersion liquid in which titanium oxide-containing porous particles are dispersed in an alcohol (porous particle dispersion liquid).
By the amount of the titanium alkoxide added in the preparation of a dispersion liquid, the primary particle diameter of the porous particles can be controlled. The larger the amount of the titanium alkoxide added, the smaller the primary particle diameter of the porous particles. A mass ratio of the titanium alkoxide to the alcohol is, for example, preferably equal to or higher than 0.04 and equal to or lower than 0.65, and more preferably equal to or higher than 0.1 and equal to or lower than 0.5.
Examples of the titanium alkoxide used in the preparation of a dispersion liquid include an alkoxy titanium chelate obtained by chelating some of alkoxy groups of tetraalkoxytitanium such as tetramethoxytitanium, tetraethoxytitanium, tetrapropoxytitanium, or tetrabutoxytitanium, di-i-propoxy-bis (ethylacetate) titanium, di-i-propoxy-bis (acetylacetonate) titanium, and the like. One kind of each of these may be used singly, or two or more kinds of these may be used in combination.
The titanium oxide aerogel particles may contain small amounts of metal elements other than titanium, such as silicon or aluminum. In this case, tetraalkoxysilane such as tetramethoxysilane, tetraethoxysilane, tetrapropoxysilane, or tetrabutoxysilane, alkyl trialkoxysilane such as methyl trimethoxysilane, methyl triethoxysilane, or ethyl triethoxysilane, alkyl dialkoxysilane such as dimethyl dimethoxysilane or dimethyl diethoxysilane, aluminum alkoxide such as aluminum isopropoxide, and the like may also be used. In a case where the particles contain a silicon element, Si/Ti which is an elementary ratio between silicon and titanium can be within a range of 0 to 0.05.
Examples of the alcohol used in the preparation of a dispersion liquid include methanol, ethanol, propanol, butanol, and the like. One kind of each of these may be used singly, or two or more kinds of these may be used in combination.
Examples of the acid in the aqueous solution of an acid used in the preparation of a dispersion liquid include oxalic acid, acetic acid, hydrochloric acid, nitric acid, and the like. The acid concentration in the aqueous solution of an acid is, for example, preferably equal to or higher than 0.001% by mass and equal to or lower than 1% by mass, and more preferably equal to or higher than 0.005% by mass and equal to or lower than 0.01% by mass.
In the preparation of a dispersion liquid, the amount of the aqueous solution of an acid added dropwise with respect to 100 parts by mass of the titanium alkoxide is, for example, preferably equal to or greater than 0.001 parts by mass and equal to or smaller than 0.1 parts by mass.
For example, in the porous particle dispersion liquid obtained by the preparation of a dispersion liquid, the concentration of solid contents is preferably equal to or higher than 1% by mass and equal to or lower than 30% by mass.
(2) Removal of Solvent
In the removal of a solvent, supercritical carbon dioxide is brought into contact with the dispersion liquid containing the porous particles and a solvent, thereby removing the solvent. Compared to a solvent removing treatment performed by heating, the solvent removing treatment performed using supercritical carbon dioxide hardly causes crushing or blocking of the porous particles. In the removal of a solvent, the solvent is removed using supercritical carbon dioxide. Therefore, it is possible to obtain titanium oxide aerogel particles having a BET specific surface area equal to or greater than 120 m2/g.
Specifically, the removal of a solvent is performed by the following operation, for example.
The porous particle dispersion liquid is put into an airtight reactor, and then liquid carbon dioxide is introduced into the reactor. Thereafter, the airtight reactor is heated, and the internal pressure of the airtight reactor is increased using a high-pressure pump such that the carbon dioxide in the airtight reactor becomes in a supercritical state. Furthermore, liquid carbon dioxide is caused to flow into the airtight reactor such that the supercritical carbon dioxide flows out of the airtight reactor. In this way, the supercritical carbon dioxide flows in the porous particle dispersion liquid in the airtight reactor. While the supercritical carbon dioxide is flowing in the porous particle dispersion liquid, the solvent is dissolved in the supercritical carbon dioxide and is removed along with the supercritical carbon dioxide flowing out of the airtight reactor.
The internal temperature and pressure of the airtight reactor are set such that carbon dioxide becomes in a supercritical state. The critical points of carbon dioxide are 31.1° C./7.38 MPa. Therefore, the internal temperature of the reactor is set to be equal to or greater than 50° C. and equal to or lower than 200° C., and the internal pressure of the reactor is set to be equal to or higher than 10 MPa and equal to or lower than 30 MPa.
—Untreated Silica-Titania Composite Aerogel Particles—
The untreated silica-titania composite aerogel particles contain a silica-titania complex, which is a composite oxide of silicon and titanium, as a main component (component taking up the highest proportion among all the components of the particles).
In the untreated silica-titania composite aerogel particles, from the viewpoint of expressing a photocatalytic function in the range of visible light, the value of Si/Ti which is an elementary ratio between silicon and titanium is, for example, preferably higher than 0 and equal to or lower than 6, more preferably equal to or higher than 0.05 and equal to or lower than 4, and even more preferably equal to or higher than 0.1 and equal to or lower than 3.
The elementary ratio (Si/Ti) between silicon atoms and titanium atoms is determined by creating elementary profiles of the silica-titania complex by performing qualitative analysis (wide scan analysis) of XPS. Specifically, Si/Ti is determined as below.
By using an XPS analyzer, in the following settings, qualitative analysis (wide scan analysis) is performed in a state of etching the silica-titania complex from the surface thereof in a depth direction, thereby identifying and quantifying titanium atoms, silicon atoms, and carbon atoms. From the obtained data, for titanium atoms, silicon atoms, and carbon atoms, elementary profiles with ordinate showing peak intensity and abscissa showing etching time are created. Each of the profile curves is divided into a plurality of regions based on a point of inflection, a region (region A which will be described later) where the peak intensity of the titanium atoms and the peak intensity of the silicon atoms are substantially the same as each other is specified, and the elementary ratio Si/Ti in this region is determined.
In the untreated silica-titania composite aerogel particles, the total content of the silica component and the titania component with respect to the total mass of the complex is, for example, preferably equal to or greater than 80% by mass, more preferably equal to or greater than 90% by mass, and even more preferably equal to or greater than 95% by mass.
Each of the untreated silica-titania composite aerogel particles may be a particle having a mother particle, in which the elementary ratio Si/Ti between silicon and titanium is higher than 0 and equal to or lower than 6, and a titania layer (layer formed of titania) present on the surface of the mother particle. That is, each of the untreated silica-titania composite aerogel particles may be a particle having a titania layer as a surface layer. In a case where these particles are used, the photocatalytic function is improved.
From the viewpoint of expressing a high photocatalytic function, the BET specific surface area of the silica-titania composite aerogel particles is, for example, preferably equal to or greater than 200 m2/g and equal to or smaller than 1,200 m2/g, more preferably equal to or greater than 300 m2/g and equal to or smaller than 1,100 m2/g, and even more preferably equal to or greater than 400 m2/g and equal to or smaller than 1,000 m2/g. The BET specific surface area of the silica-titania composite aerogel particles is determined by a gas adsorption method using a nitrogen gas.
As a manufacturing method of the untreated silica-titania composite aerogel particles, although there is no particular limitation, a sol-gel method in which alkoxysilane and a titanium alkoxide are used as materials is preferable.
Although there is no particular limitation, it is preferable that the untreated silica-titania composite aerogel particles are formed of a hydrolysis condensate of alkoxysilane and a titanium alkoxide. Here, in some cases, a portion of a hydrocarbon group in an alkoxy group of the alkoxysilane or the titanium alkoxide remains in the complex in an unreacted state.
Hereinafter, a manufacturing method of the untreated silica-titania composite aerogel particles will be described.
Although there is no particular limitation, it is preferable that the manufacturing method of the untreated silica-titania composite aerogel particles includes at least the following (1′) and (2′).
(1′) Making porous particles containing silica-titania complex by sol-gel method and preparing dispersion liquid containing the porous particles and solvent (preparation of dispersion liquid)
(2′) Removing the solvent from the dispersion liquid by using supercritical carbon dioxide (removal of solvent)
(1′) Preparation of Dispersion Liquid
In the preparation of a dispersion liquid, for example, by using alkoxysilane and a titanium alkoxide as materials, a silica-titania complex is generated by causing reactions (hydrolysis and condensation) between the materials, thereby obtaining a dispersion liquid in which porous particles containing the silica-titania complex are dispersed in a solvent. Although there is no particular limitation, it is preferable that the porous particles are aggregated particles in which primary particles containing the silica-titania complex are aggregated while forming a porous structure.
Specifically, the preparation of a dispersion liquid is performed as below.
Alkoxysilane and a titanium alkoxide are added to an alcohol and stirred, and in this state, an aqueous solution of an acid is added dropwise thereto such that the alkoxysilane and the titanium oxide react with each other and generate a silica-titania complex, thereby obtaining a dispersion liquid in which silica-titania complex-containing porous particles are dispersed in an alcohol (porous particle dispersion liquid).
By controlling the mixing ratio between the alkoxysilane and the titanium oxide in the preparation of a dispersion liquid, it is possible to control the elementary ratio Si/Ti between silicon and titanium in the untreated silica-titania composite aerogel particles.
In the preparation of a dispersion liquid, by the total amount of the alkoxysilane and the titanium alkoxide with respect to the amount of alcohol, it is possible to control the particle diameter of primary particles constituting the untreated silica-titania aerogel particles and the particle diameter of the untreated silica-titania aerogel particles. The larger the total amount with respect to the amount of alcohol, the smaller the particle diameter of primary particles constituting the untreated silica-titania composite aerogel particles, and the larger the particle diameter of the untreated silica-titania composite aerogel particles. The total amount of the alkoxysilane and the titanium alkoxide with respect to 100 parts by mass of the alcohol is, for example, preferably equal to or greater than 4 parts by mass and equal to or smaller than 250 parts by mass, and more preferably equal to or greater than 10 parts by mass and equal to or smaller than 50 parts by mass.
Examples of the alkoxysilane used in the preparation of a dispersion liquid include tetraalkoxysilane such as tetramethoxysilane, tetraethoxysilane, tetrapropoxysilane, or tetrabutoxysilane, alkyl trialkoxysilane such as methyl trimethoxysilane, methyl triethoxysilane, or ethyl triethoxysilane, alkyl dialkoxysilane such as dimethyl dimethoxysilane or dimethyl diethoxysilane, and the like. One kind of each of these may be used singly, or two or more kinds of these may be used in combination.
Examples of the titanium alkoxide used in the preparation of a dispersion liquid include an alkoxytitanium chelate obtained by chelating some of alkoxy groups of tetraalkoxy titanium such as tetramethoxytitanium, tetraethoxytitanium, tetrapropoxytitanium, or tetrabutoxytitanium, di-i-propoxy-bis (ethylacetacetate) titanium, di-i-propoxy-bis (acetylacetonate) titanium, and the like. One kind of each of these may be used singly, or two or more kinds of these may be used in combination.
Examples of the alcohol used in the preparation of a dispersion liquid include methanol, ethanol, propanol, butanol, and the like. One kind of each of these may be used singly, or two or more kinds thereof may be used in combination.
Examples of the acid in the aqueous solution of an acid used in the preparation of a dispersion liquid include oxalic acid, acetic acid, hydrochloric acid, nitric acid, and the like. The acid concentration in the aqueous solution of an acid is, for example, preferably equal to or higher than 0.001% by mass and equal to or lower than 1% by mass, and more preferably equal to or higher than 0.005% by mass and equal to or lower than 0.01% by mass.
In the preparation of a dispersion liquid, the amount of the aqueous solution of an acid added dropwise with respect to a total of 100 parts by mass of the alkoxysilane and the titanium alkoxide is, for example, preferably equal to or greater than 0.001 parts by mass and equal to or smaller than 0.1 parts by mass.
For example, in the porous particle dispersion liquid obtained by the preparation of a dispersion liquid, the concentration of solid contents is preferably equal to or higher than 1% by mass and equal to or lower than 30% by mass.
(2′) Removal of Solvent
In the removal of a solvent, supercritical carbon dioxide is brought into contact with the dispersion liquid containing the porous particles and a solvent, thereby removing the solvent. Compared to a solvent removing treatment performed by heating, the solvent removing treatment performed using supercritical carbon dioxide hardly causes crushing or blocking of the pores of the porous particles (particularly, aggregated particles in which primary particles are aggregated while forming a porous structure). In the removal of a solvent, the solvent is removed using supercritical carbon dioxide. Therefore, it is possible to obtain untreated silica-titania composite aerogel particles having a BET specific surface area equal to or greater than 200 m2/g.
Specifically, the removal of a solvent is performed by the following operation, for example.
The porous particle dispersion liquid is put into an airtight reactor, and then liquid carbon dioxide is introduced into the reactor. Thereafter, the airtight reactor is heated, and the internal pressure of the airtight reactor is increased using a high-pressure pump such that the carbon dioxide in the airtight reactor becomes in a supercritical state. Furthermore, liquid carbon dioxide is caused to flow into the airtight reactor such that the supercritical carbon dioxide flows out of the airtight reactor. In this way, the supercritical carbon dioxide flows in the porous particle dispersion liquid in the airtight reactor. While the supercritical carbon dioxide is flowing in the porous particle dispersion liquid, the solvent is dissolved in the supercritical carbon dioxide and is removed along with the supercritical carbon dioxide flowing out of the airtight reactor.
The internal temperature and pressure of the airtight reactor are set such that carbon dioxide becomes in a supercritical state. The critical points of carbon dioxide are 31.1° C./7.38 MPa. Therefore, the internal temperature of the reactor is set to be equal to or greater than 50° C. and equal to or lower than 200° C., and the internal pressure of the reactor is set to be equal to or higher than 10 MPa and equal to or lower than 30 MPa.
In a case where particles each having a titania layer on the surface thereof are manufactured as the untreated silica-titania composite aerogel particles, it is better to perform the following (i) and (ii) in (1′) preparation of dispersion liquid.
(i) Alkoxysilane and a titanium alkoxide are added to an alcohol and stirred, and in this state, an aqueous solution of an acid is added dropwise thereto such that the alkoxysilane and the titanium oxide react with each other and generate a silica-titania complex, thereby obtaining a dispersion liquid in which mother particles containing a silica-titania complex are dispersed in an alcohol (first dispersion liquid).
(ii) A mixed solution obtained by mixing an alcohol with a titanium alkoxide is added dropwise to the first dispersion liquid with stirring such that the mother particles and the titanium alkoxide react with each other and generate porous particles in which an interlayer is formed on the surface of the mother particles, thereby obtaining a dispersion liquid in which the porous particles are dispersed in an alcohol (second dispersion liquid).
(Organic Metal Compound)
The organic metal compound is a metal compound having a metal atom and a hydrocarbon group.
From the viewpoint of more easily expressing responsiveness to visible light, although there is no particular limitation, it is preferable that the organic metal compound is a metal compound formed only of a metal atom, a carbon atom, a hydrogen atom, and an oxygen atom.
From the viewpoint of more easily expressing responsiveness to visible light, although there is no particular limitation, it is preferable that the organic metal compound is bonded to the surface of each of the particles through an oxygen atom O directly bonded to a metal atom M in the organic metal compound, in other words, it is preferable that the organic metal compound is bonded to the surface of each of the particles through a covalent bond represented by M-O—Ti (in a case where the titanium-based compound particles are silica-titania composite aerogel particles, the covalent bond is M-O—Ti or M-O—Si).
From the viewpoint of more easily adsorbing germs and from the viewpoint of more easily expressing responsiveness to visible light, as the organic metal compound, for example, an organic metal compound having a metal atom M and a hydrocarbon group directly bonded to the metal atom M are preferable. Although there is no particular limitation, it is preferable that the organic metal compound is bonded to the surface of each of the particles through an oxygen atom O directly bonded to the metal atom M in the organic metal compound. That is, from the viewpoint of more easily adsorbing germs and from the viewpoint of more easily expressing responsiveness to visible light, although there is no particular limitation, it is preferable that a structure, in which a hydrocarbon group, the metal atom M, the oxygen atom O, and a titanium atom Ti are connected to each other in this order through a covalent bond (a hydrocarbon group-M-O—Ti (in a case where the titanium-based compound particles are silica-titania composite aerogel particles, hydrocarbon group-M-O-TI or hydrocarbon group-M-O—Si)), is present on the surface of the particles.
In a case where the organic metal compound has a plurality of hydrocarbon groups, although there is no particular limitation, it is preferable that at least one hydrocarbon group is directly bonded to the metal atom in the organic metal compound.
The state where the atoms are chemically bonded to each other in the organic metal compound can be ascertained by performing high-resolution analysis (narrow scan analysis) of X-ray Photoelectron Spectroscopy (XPS).
As the metal atom M in the organic metal compound, although there is no particular limitation, a silicon atom, an aluminum atom, or a titanium atom is preferable, a silicon atom or an aluminum atom is more preferable, and a silicon atom is particularly preferable.
Examples of the hydrocarbon group that the organic metal compound has include a saturated or unsaturated aliphatic hydrocarbon group having 1 to 40 carbon atoms (for example, preferably having 1 to 20 carbon atoms, more preferably having 1 to 18 carbon atoms, even more preferably having 4 to 12 carbon atoms, and still more preferably having 4 to 10 carbon atoms) and an aromatic hydrocarbon group having 6 to 27 carbon atoms (for example, preferably having 6 to 20 carbon atoms, more preferably having 6 to 18 carbon atoms, even more preferably having 6 to 12 carbon atoms, and particularly preferably having 6 to 10 carbon atoms).
From the viewpoint of expressing a high photocatalytic function and improving dispersibility, the hydrocarbon group that the organic metal compound has is, for example, preferably an aliphatic hydrocarbon group, more preferably a saturated aliphatic hydrocarbon group, and particularly preferably an alkyl group. The aliphatic hydrocarbon group may be any of linear, branched, and cyclic aliphatic hydrocarbon groups. From the viewpoint of dispersibility, the aliphatic hydrocarbon group is, for example, preferably a linear or branched aliphatic hydrocarbon group. The number of carbon atoms in the aliphatic hydrocarbon group is, for example, preferably equal to or greater than 1 and equal to or smaller than 20, more preferably equal to or greater than 1 and equal to or smaller than 18, even more preferably equal to or greater than 4 and equal to or smaller than 12, and particularly preferably equal to or greater than 4 and equal to or smaller than 10.
As the organic metal compound, although there is no particular limitation, a silane compound having a hydrocarbon group is particularly preferable. Examples of the silane compound having a hydrocarbon include a chlorosilane compound, an alkoxysilane compound, and the like.
From the viewpoint of expressing a high photocatalytic function and improving dispersibility, as the silane compound having a hydrocarbon group, although there is no particular limitation, a compound represented by Formula (1): R1nSiR2n is preferable.
In Formula (1): R1nSiR2m, R1 represents a saturated or unsaturated aliphatic hydrocarbon group having 1 to 20 carbon atoms or an aromatic hydrocarbon group having 6 to 20 carbon atoms, R2 represents a halogen atom or an alkoxy group, n represents an integer equal to or greater than 1 and equal to or smaller than 3, m represents an integer equal to or greater than 1 and equal to or smaller than 3, and n+m=4. In a case where n is an integer 2 or 3, a plurality of R1's may be the same groups or different groups. In a case where m is an integer 2 or 3, a plurality of R2's may be the same groups or different groups.
The aliphatic hydrocarbon group represented by R1 may be any of linear, branched, and cyclic aliphatic hydrocarbon groups. From the viewpoint of dispersibility, the aliphatic hydrocarbon group is, for example, preferably a linear or branched aliphatic hydrocarbon group. From the viewpoint of expressing a high photocatalytic function and improving dispersibility, the number of carbon atoms in the aliphatic hydrocarbon group is, for example, preferably equal to or greater than 1 and equal to or smaller than 20, more preferably equal to or greater than 1 and equal to or smaller than 18, even more preferably equal to or greater than 4 and equal to or smaller than 12, and still more preferably equal to or greater than 4 and equal to or smaller than 10. The aliphatic hydrocarbon group may be any of saturated and unsaturated aliphatic hydrocarbon groups. From the viewpoint of expressing a high photocatalytic function and improving dispersibility, the aliphatic hydrocarbon group is, for example, preferably a saturated aliphatic hydrocarbon group, and more preferably an alkyl group.
Examples of the saturated aliphatic hydrocarbon group include a linear alkyl group (a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, a hexyl group, a heptyl group, an octyl group, a nonyl group, a decyl group, a dodecyl group, a hexadecyl group, an eicosyl group, or the like), a branched alkyl group (an isopropyl group, an isobutyl group, an isopentyl group, a neopentyl group, a 2-ethylhexyl group, a t-butyl group, a t-pentyl group, an isopentadecyl group, or the like), a cycloalkyl group (a cyclopropyl group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cyclooctyl group, a tricyclodecyl group, a norbornyl group, an adamantyl group, or the like), and the like.
Examples of the unsaturated aliphatic hydrocarbon group include an alkenyl group (a biphenyl group (ethenyl group), a 1-propenyl group, a 2-propenyl group, a 2-butenyl group, a 1-butenyl group, a 1-hexenyl group, a 2-dodecenyl group, a pentenyl group, or the like), an alkynyl group (an ethynyl group, a 1-propynyl group, a 2-propynyl group, a 1-butynyl group, a 3-hexynyl group, a 2-dodecynyl group, or the like), and the like.
The aliphatic hydrocarbon group also includes a substituted aliphatic hydrocarbon group. Examples of the substituent which can substitute the aliphatic hydrocarbon group include a halogen atom, an epoxy group, a glycidyl group, a glycidoxy group, a mercapto group, a methacryloyl group, an acryloyl group, and the like.
The number of carbon atoms in the aromatic hydrocarbon group represented by R1 is, for example, preferably equal to or greater than 6 and equal to or smaller than 20, more preferably equal to or greater than 6 and equal to or smaller than 18, even more preferably equal to or greater than 6 and equal to or smaller than 12, and still more preferably equal to or greater than 6 and equal to or smaller than 10.
Examples of the aromatic hydrocarbon group include a phenylene group, a biphenylene group, a terphenylene group, a naphthalene group, an anthracene group, and the like.
The aromatic hydrocarbon group also includes a substituted aromatic hydrocarbon group. Examples of the substituent which can substitute the aromatic hydrocarbon group include a halogen atom, an epoxy group, a glycidyl group, a glycidoxy group, a mercapto group, a methacryloyl group, an acryloyl group, and the like.
Examples of the halogen atom represented by R2 include a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, and the like. As the halogen atom, although there is no particular limitation, a chlorine atom, a bromine atom, or an iodine atom is preferable.
Examples of the alkoxy group represented by R2 include an alkoxy group having 1 to 10 carbon atoms (for example, preferably having 1 to 8 carbon atoms, and more preferably having 3 to 8 carbon atoms). Examples of the alkoxy group include a methoxy group, an ethoxy group, an isopropoxy group, a t-butoxy group, a n-butoxy group, a n-hexyloxy group, a 2-ethylhexyloxy group, a 3,5,5-trimethylhexyloxy group, and the like. The alkoxy group also includes a substituted alkoxy group. Examples of the substituent which can substitute the alkoxy group include a halogen atom, a hydroxyl group, an amino group, an alkoxy group, an amide group, a carbonyl group, and the like.
From the viewpoint of expressing a high photocatalytic function and improving dispersibility, as the compound represented by Formula (1): R1 nSiR2m, although there is no particular limitation, a compound in which R′ is a saturated aliphatic hydrocarbon group is preferable. Particularly, as the compound represented by Formula (1): R1 nSiR2m, although there is no particular limitation, a compound is preferable in which R1 is a saturated aliphatic hydrocarbon group having 1 to 20 carbon atoms, R2 is a halogen atom or an alkoxy group, n is an integer equal to or greater than 1 and equal to or smaller than 3, m is an integer equal to or greater than 1 and equal to or smaller than 3, and n+m=4.
Examples of the compound represented by Formula (1): R1nSiR2m include silane compounds such as vinyltrimethoxysilane, methyltrimethoxysilane, ethyltrimethoxysilane, propyltrimethoxysilane, butyltrimethoxysilane, hexyltrimethoxysilane, n-octyltrimethoxysilane, decyltrimethoxysilane, dodecyltrimethoxysilane, vinyltriethoxysilane, methyltriethoxysilane, ethyltriethoxysilane, butyltriethoxysilane, hexyltriethoxysilane, decyltriethoxysilane, dodecyltriethoxysilane, phenyltrimethoxysilane, o-methylphenyltrimethoxysilane, p-methylphenyltrimethoxysilane, phenyltriethoxysilane, benzyltriethoxysilane, decyltrichlorosilane, phenyltrichlorosilane (in the above compounds, n=1, and m=3); dimethyldimethoxysilane, dimethyldiethoxysilane, methylvinyldimethoxysilane, methylvinyldiethoxysilane, diphenyldimethoxysilane, diphenyldiethoxysilane, dimethyldichlorosilane, dichlorodiphenylsilane, (in the above compounds, n=2, and m=2); trimethylmethoxysilane, trimethylethoxysilane, trimethylchlorosilane, decyldimethylchlorosilane, triphenylchlorosilane (in the above compounds, n=3, and m=1); 3-glycidoxypropyltrimethoxysilane, γ-methacryloxypropyltrimethoxysilane, γ-mercaptopropyltrimethoxysilane, γ-chloropropyltrimethoxysilane, γ-aminopropyltrimethoxysilane, γ-aminopropyltriethoxysilane, γ-(2-aminoethyl)aminopropyltrimethoxysilane, γ-(2-aminoethyl)aminopropylmethyldimethoxysilane, and γ-glycidyloxypropylmethyldimethoxysilane (in the above compounds, R1 is a substituted aliphatic hydrocarbon group or a substituted aromatic hydrocarbon group). One kind of silane compound may be used singly, or two or more kinds silane compounds may be used in combination.
From the viewpoint of expressing a high photocatalytic function and improving dispersibility, the hydrocarbon group in the silane compound represented by Formula (1) is, for example, preferably an aliphatic hydrocarbon group, more preferably a saturated aliphatic hydrocarbon group, and particularly preferably an alkyl group. From the viewpoint of expressing a high photocatalytic function and improving dispersibility, the hydrocarbon group in the above silane compound is, for example, preferably a saturated aliphatic hydrocarbon group having 1 to 20 carbon atoms, more preferably a saturated aliphatic hydrocarbon group having 1 to 18 carbon atoms, even more preferably a saturated aliphatic hydrocarbon group having 4 to 12 carbon atoms, and particularly preferably a saturated aliphatic hydrocarbon group having 4 to 10 carbon atoms.
Examples of the organic metal compound having aluminum as a metal atom include alkyl aluminate such as triethoxy aluminum, tri-i-propoxy aluminum, or tri-sec-butoxy aluminum; aluminum chelate such as di-i-propoxy.mono-sec-butoxy aluminum or di-i-propoxy aluminum.ethyl acetoacetate; an aluminate-based coupling agent such as acetoalkoxyaluminum diisopropylate; and the like.
Examples of the organic metal compound having titanium as a metal atom include a titanate-based coupling agent such as isopropyltriisostearoyl titanate, tetraoctyl bis(ditridecylphosphite)titanate, or bis(dioctylpyrophosphate)oxyacetate titanate; titanium chelate such as di-i-propoxybis(ethylacetoacetate)titanium, di-i-propoxybis(acetylacetonate)titanium, di-i-propoxybis(triethanolaminate)titanium, di-i-propoxytitanium diacetate, or di-i-propoxytitanium dipropionate; and the like.
One kind of organic metal compound may be used singly, or two or more kinds of organic metal compounds may be used in combination.
(Manufacturing Method of Photocatalyst Particles)
The manufacturing method of the photocatalyst particles is not particularly limited. For example, by treating the surface of untreated particles with an organic metal compound, the photocatalyst particles are obtained.
Hereinafter, examples of aspects of the manufacturing method of the photocatalyst particles will be described.
Although there is no particular limitation, it is preferable that the manufacturing method of the photocatalyst particles include (a) performing a surface treatment on untreated particles by using an organic metal compound and (b) performing a heating treatment in the process of or after the surface treatment performed on the untreated particles.
(a) Performing Surface Treatment
The method for performing a surface treatment on untreated particles by using an organic metal compound is not particularly limited. Examples thereof include a method of bringing an organic metal compound into direct contact with untreated particles; and a method of bringing a treatment solution, which is obtained by dissolving an organic metal compound in a solvent, into contact with untreated particles. Specifically, examples thereof include a method of adding an organic metal compound or a treatment solution to a dispersion liquid, which is obtained by dispersing untreated particles in a solvent, with stirring; and a method of adding an organic metal compound or a treatment solution (by dripping, spraying, or the like) to untreated particles in a fluid state by means of stirring using a Henschel mixer or the like. By these methods, a reactive group (for example, a hydrolysable group such as a halogeno group or an alkoxy group) in the organic metal compound reacts with a hydroxyl group present on the surface of the untreated particles, whereby the surface of the untreated particles is treated.
The surface treatment can be performed in the atmosphere or in a nitrogen atmosphere. In a case where the surface treatment is performed on titanium oxide aerogel particles or silica-titania composite aerogel particles as untreated particles, although there is no particular limitation, it is preferable to perform the surface treatment in supercritical carbon dioxide. In a case where the surface treatment is performed as above, the organic metal compound reaches a portion deep inside the pores of the porous particles, and the surface treatment is performed deep into the pores of the porous particles. Accordingly, although there is no particular limitation, it is preferable to perform the surface treatment in supercritical carbon dioxide.
The surface treatment performed in supercritical carbon dioxide is carried out, for example, by mixing and reacting together the organic metal compound and the porous substance in supercritical carbon dioxide with stirring. In addition, the surface treatment is carried out, for example, by preparing a treatment solution by means of mixing together the organic metal compound and a solvent and mixing together the porous substance and the treatment solution in supercritical carbon dioxide with stirring. In order to increase the specific surface area while maintaining the porous structure of the porous substance, although there is no particular limitation, it is preferable to add the organic metal compound to supercritical carbon dioxide after the finish of the removal of a solvent, and to cause the organic metal compound to react with the surface of the porous substance in the supercritical carbon dioxide.
Examples of the solvent dissolving the organic metal compound include an organic solvent (for example, a hydrocarbon-based solvent, an ester-based solvent, an ether-based solvent, a halogen-based solvent, an alcohol-based solvent, or the like), water, a mixed solvent of these, and the like. Examples of the hydrocarbon-based solvent include toluene, benzene, xylene, hexane, octane, hexadecane, cyclohexane, and the like. Examples of the ester-based solvent include methyl acetate, ethyl acetate, isopropyl acetate, amyl acetate, and the like. Examples of the ether-based solvent include dibutyl ether, dibenzyl ether, and the like. Examples of the halogen-based solvent include 1,1-dichloro-1-fluoroethane, 1,1-dichloro-2,2,2-trifluoroethane, 1,1-dichloro-2,2,3,3,3-pentafluoropropane, chloroform, dichloroethane, carbon tetrachloride, and the like. Examples of the alcohol-based solvent include methanol, ethanol, i-propyl alcohol, and the like. Examples of the water include tap water, distilled water, pure water, and the like. As the solvent, in addition to these, solvents such as dimethyl formamide, dimethyl acetamide, dimethyl sulfoxide, acetic acid, and sulfuric acid may also be used.
In the treatment solution obtained by dissolving the organic metal compound in a solvent, the concentration of the organic metal compound is, for example, preferably equal to or higher than 0.05 mol/L and equal to or lower than 500 mol/L, and more preferably equal to or higher than 0.5 mol/L and equal to or lower than 10 mol/L.
From the viewpoint of expressing a high photocatalytic function and improving dispersibility, it is better that the surface treatment performed on the particles by using an organic metal compound is carried out under the following conditions. It is better that the surface treatment is performed on untreated particles by using an organic metal compound in an amount equal to or greater than 10% by mass and equal to or smaller than 100% by mass (for example, preferably equal to or greater than 20% by mass and equal to or smaller than 75% by mass, and more preferably equal to or greater than 25% by mass and equal to or smaller than 50% by mass) with respect to the untreated particles. In a case where the amount of the organic metal compound is equal to or greater than 10% by mass, a high photocatalytic function is more easily expressed even in the range of visible light, and dispersibility is easily improved. In a case where the amount of the organic metal compound is equal to or smaller than 100% by mass, the amount of metals, which are present on the surface of the particles and derived from the organic metal compound, is inhibited from increasing too much, and the deterioration of the photocatalytic function resulting from an excess of metal is inhibited.
The temperature of the surface treatment performed on the untreated particles by using the organic metal compound is, for example, preferably equal to or higher than 15° C. and equal to or lower than 150° C., and more preferably equal to or higher than 20° C. and equal to or lower than 100° C. The surface treatment time is, for example, preferably equal to or longer than 10 minutes and equal to or shorter than 120 minutes, and more preferably equal to or longer than 30 minutes and equal to or shorter than 90 minutes.
Here, in a case where the surface treatment is performed in supercritical carbon dioxide, the temperature and pressure for the surface treatment are set such that the carbon dioxide becomes in a supercritical state. For example, the surface treatment is performed in an atmosphere with a temperature equal to or higher than 50° C. and equal to or lower than 200° C. under a pressure equal to or higher than 10 MPa and equal to or lower than 30 MPa. The reaction time is, for example, preferably equal to or longer than 10 minutes and equal to or shorter than 24 hours, more preferably equal to or longer than 20 minutes and equal to or shorter than 120 minutes, and even more preferably equal to or longer than 30 minutes and equal to or shorter than 90 minutes.
After the surface treatment performed on the untreated particles by using the organic metal compound, it is better to perform a drying treatment. The drying treatment method is not particularly limited, and for example, known drying methods such as a vacuum drying method and a spray drying method are used. The drying temperature is, for example, preferably equal to or higher than 20° C. and equal to or lower than 150° C.
Here, in a case where the surface treatment is performed in supercritical carbon dioxide, for example, the solvent is preferably removed from the dispersion liquid containing the porous particles by using supercritical carbon dioxide, and more preferably removed by allowing supercritical carbon dioxide to flow in supercritical carbon dioxide after the finish of the surface treatment.
(b) Performing Heating Treatment
The heating treatment is performed while the surface treatment is being performed on the untreated particles or after the surface treatment is performed on the untreated particles.
The heating treatment can be performed at the time of carrying out the surface treatment on the untreated particles by using the organic metal compound; performed at the time of carrying out the drying treatment after the surface treatment; or separately performed after the drying treatment. For example, the heating treatment is preferably performed at the time of carrying out the drying treatment after the surface treatment or separately performed after the drying treatment from the viewpoint of thoroughly reacting the particles with the organic metal compound before the heat treatment, and more preferably separately performed after the drying treatment from the viewpoint of appropriately carrying out the drying treatment.
From the viewpoint of expressing a high photocatalytic function and improving dispersibility, the temperature of the heating treatment is, for example, preferably equal to or higher than 180° C. and equal to or lower than 500° C., more preferably equal to or higher than 200° C. and equal to or lower than 450° C., and even more preferably equal to or higher than 250° C. and equal to or lower than 400° C. From the viewpoint of expressing a high photocatalytic function and improving dispersibility, the time of the heating treatment is, for example, preferably equal to or longer than 10 minutes and equal to or shorter than 300 minutes, and more preferably equal to or longer than 30 minutes and equal to or shorter than 120 minutes. In a case where the heating treatment is performed while the surface treatment is being performed on the untreated particles, although there is no particular limitation, it is preferable to first allow the organic metal compound to thoroughly react at the temperature of the surface treatment and then perform the heating treatment at the temperature of the heating treatment. In a case where the heating treatment is performed during the drying treatment after the surface treatment, the drying treatment is performed at the temperature of the heating treatment.
In a case where the temperature of the heating treatment is equal to or higher than 180° C. and equal to or lower than 500° C., particles expressing a high photocatalytic function even in the range of visible light are efficiently obtained. Presumably, in a case where the heating treatment is performed at a temperature equal to or higher than 180° C. and equal to or lower than 500° C., the hydrocarbon group derived from the metal compound present on the surface of the particles may be appropriately oxidized, and some of the C—C bonds or C═C bonds may change to C—O bonds or C═O bonds.
Although there is no particular limitation, it is preferable that the heating treatment is performed in an atmosphere with an oxygen concentration (% by volume) equal to or higher than 1% and equal to or lower than 21%. In a case where the heating treatment is performed in such an oxygen atmosphere, the hydrocarbon group derived from the metal compound present on the surface of the particles can be appropriately and efficiently oxidized. For example, the oxygen concentration (% by volume) is more preferably equal to or higher than 3% and equal to or lower than 21%, and even more preferably equal to or higher than 5% and equal to or lower than 21%.
The heating treatment method is not particularly limited. For example, known methods such as heating performed using an electric furnace, a kiln (a roller hearth kiln, a shuttle kiln, or the like), a radiation-type heating furnace, or the like; and heating performed using laser light, infrared rays, UV, microwaves, or the like are used.
Through the steps described so far, the photocatalyst particles are obtained.
(Characteristics of Photocatalyst Particles)
The photocatalyst particles have absorption at a wavelength of 500 nm in a visible absorption spectrum.
From the viewpoint of expressing a high photocatalytic function even in the range of visible light, in a visible absorption spectrum, for example, the photocatalyst particles preferably have absorption at a wavelength of 450 nm and a wavelength of 500 nm, more preferably have absorption at a wavelength of 450 nm, a wavelength of 500 nm, and a wavelength of 550 nm, even more preferably have absorption at a wavelength of 450 nm, a wavelength of 500 nm, a wavelength of 550 nm, and a wavelength of 600 nm, and particularly preferably have absorption at a wavelength of 450 nm, a wavelength of 500 nm, a wavelength of 550 nm, a wavelength of 600 nm, and a wavelength of 700 nm.
From the viewpoint of expressing a high photocatalytic function even in the range of visible light, in a visible absorption spectrum, for example, the photocatalyst particles preferably have absorption in the entire range of a wavelength equal to or longer than 450 nm and equal to or shorter than 500 nm, more preferably have absorption in the entire range of a wavelength equal to or longer than 400 nm and equal to or shorter than 550 nm, even more preferably ha have s absorption in the entire range of a wavelength equal to or longer than 400 nm and equal to or shorter than 600 nm, and particularly preferably have absorption in the entire range of a wavelength equal to or longer than 400 nm and equal to or shorter than 700 nm.
From the viewpoint of expressing a high photocatalytic function even in the range of visible light, provided that an absorbance at a wavelength of 350 nm in an ultraviolet-visible absorption spectrum is 1, the absorbance of the photocatalyst particles at each wavelength in a visible absorption spectrum is preferably as below, for example.
Absorbance at wavelength of 700 nm: equal to or higher than 0.02, preferably equal to or higher than 0.05, and more preferably equal to or higher than 0.08, for example
From the viewpoint of expressing a high photocatalytic function even in the range of visible light, in a visible absorption spectrum, a ratio of absorbance of the photocatalyst particles at a wavelength of 550 nm to the absorbance thereof at a wavelength of 450 nm (550 nm/450 nm) is, for example, preferably equal to or higher than 0.1, more preferably equal to or higher than 0.2, even more preferably equal to or higher than 0.3, and still more preferably equal to or higher than 0.4.
The titanium-based compound particles as the photocatalyst particles tend to exhibit ultraviolet absorbing properties. The photocatalyst particles, which are obtained by performing surface modification on the titanium-based compound particles and exhibit responsiveness to visible light, particularly relatively strongly absorb blue light having a wavelength close to that of ultraviolet rays among visible lights. Therefore, in a case where the ratio of absorbance represented by 550 nm/450 nm is equal to or higher than 0.1, it is understood that the titanium-based compound particles are sufficiently surface-modified as visible range-responsive photocatalyst particles.
The ratio of absorbance, represented by 550 nm/450 nm, of the visible light-responsive photocatalyst particles obtained by performing surface modification on the titanium-based compound particles tends to be less than 1. The ratio of absorbance of the photocatalyst particles tends to be equal to or lower than 0.8.
The ultraviolet-visible absorption spectrum of the photocatalyst particles is obtained by the following method. Particles to be measured are dispersed in tetrahydrofuran, then applied onto a glass substrate, and dried in the atmosphere at 24° C. By using a spectrophotometer (for example, U-4100 manufactured by Hitachi High-Technologies Corporation, scan speed: 600 nm/min, slit width: 2 nm, sampling interval: 1 nm), in a diffuse reflective disposition, a diffuse reflectance spectrum in a wavelength range of 200 nm to 900 nm is measured. From the diffuse reflectance spectrum, absorbance at each wavelength is theoretically determined by Kubelka-Munk transformation.
The glass substrate is affected by the film thickness of the applied particles or the like, and hence an error may occur in the measured value. Therefore, the measured value is corrected. That is, an absorbance at 900 nm is subtracted from the absorbance at each wavelength, and the obtained value is adopted as an absorbance at each wavelength.
In an infrared absorption spectrum, the photocatalyst particles have an absorption peak in a range of wave number equal to or greater than 2,700 cm−1 and equal to or smaller than 3,000 cm−1.
Specifically, in an infrared absorption spectrum, for example, it is preferable that the photocatalyst particles have at least one absorption peak in a range of wave number equal to or greater 2,700 cm−1 and equal to or smaller than 3,000 cm−1. Having an absorption peak means having absorption with absorption intensity (absorbance) equal to or higher than 0.022 (5% in terms of transmittance).
The infrared absorption spectrum of the photocatalyst particles is measured by the following method. First, the photocatalyst particles to be measured are prepared as a measurement sample by a KBr tablet preparation method. Then, by using an infrared spectrophotometer (manufactured by JASCO Corporation: FT-IR-410), the measurement sample is measured within a range of wave number equal to or greater than 500 cm−1 and equal to or smaller than 4,000 cm−1 under the conditions of the number of times of accumulation of 300 and resolution of 4 cm−1, thereby obtaining an infrared absorption spectrum.
The average primary particle diameter of the photocatalyst particles is, for example, equal to or greater than 1 nm and equal to or smaller than 200 nm, more preferably equal to or greater than 5 nm and equal to or smaller than 150 nm, and even more preferably equal to or greater than 10 nm and equal to or smaller than 100 nm. In a case where the average primary particle diameter of the photocatalyst particles is equal to or greater than 1 nm, the particles are hardly aggregated, and the photocatalytic function is easily enhanced. In a case where the average primary particle diameter of the photocatalyst particles is equal to or smaller than 200 nm, the ratio of the specific surface area to the amount is increased, and hence the photocatalytic function is easily enhanced. Therefore, in a case where the average primary particle diameter of the photocatalyst particles is within the above range, a high photocatalytic function is easily expressed in the range of visible light.
The average primary particle diameter of the photocatalyst particles is a value measured by the following measurement method. The photocatalyst particles are observed and imaged using a scanning electron microscope (manufactured by Hitachi, LTD., S-4100). The captured image is input into an image analyzer (manufactured by NIRECO., LUZEX III), the area of each particle is determined by image analysis, and an equivalent circle diameter (nm) is determined from the area. The arithmetic mean of equivalent circle diameters of 100 primary particles is calculated and adopted as the average diameter of the primary particles.
In a case where the photocatalyst particles are silica-titania composite aerogel particles, as the photocatalyst particles, it is better to use particles obtained by performing a surface treatment on untreated silica-titania composite aerogel particles having a titania layer as a surface layer by using an organic metal compound.
Specifically, each of these particles has a mother particle (for example, a mother particle in which an elementary ratio Si/Ti between silicon and titanium is higher than 0 and equal to or lower than 6), a titania layer present on the surface of the mother particle (hereinafter, referred to as “interlayer” as well), and a layer which is formed on the surface of the titania layer by bonding of a metal compound having a metal atom and a hydrocarbon group to the surface through an oxygen atom (that is, a layer containing a metal compound having a metal atom and a hydrocarbon group, hereinafter, referred to as “surface layer” as well).
Whether each of the silica-titania composite aerogel particles has the layers described above can be checked by the following method. Whether particles other than the silica-titania composite aerogel particles have the surface layer can also be checked by the following method.
The qualitative analysis (wide scan analysis) of XPS is performed in a state of etching the silica-titania composite aerogel particles in the depth direction from the surface thereof by using rare gas ions. In this way, at least titanium, silicon, and carbon are identified and quantified. From the obtained data, for at least each of the titanium, silicon, and carbon, an elementary profile with ordinate showing peak intensity and abscissa showing etching time is created. The profile curve is divided into a plurality of regions based on a point of inflection, and a region reflecting the elementary composition of the mother particle, a region reflecting the elementary composition of the interlayer, and a region reflecting the elementary composition of the surface layer are specified. In a case where the region reflecting the elementary composition of the interlayer is in the elementary profile, it is determined that the silica-titania composite aerogel particles have the interlayer. In a case where the region reflecting the elementary composition of the surface layer is in the elementary profile, it is determined that the silica-titania composite aerogel particles have the surface layer.
Hereinafter, the elementary profile will be described based on
Each of the elementary profiles shown in
Region A: region which exists at the last state of etching and in which peak intensity of titanium and peak intensity of silicon are substantially constant.
Region B: region which exists immediately before region A and in the peak intensity of titanium is reduced toward the particle surface while the peak intensity of silicon is increased toward the particle surface.
Region C: region which exists immediately before region B and in which peak intensity of titanium is substantially constant and substantially no silicon is detected.
Region D: region which exists at the initial stage of etching and in which peak intensity of carbon is substantially constant and no metal atom is detected.
The region A and the region B are regions reflecting the elementary composition of the mother particles. At the time of manufacturing the mother particles, silica and titania form a covalent bond at a ratio according to the mixing ratio between the alkoxysilane and the titanium alkoxide as materials of the silica-titania complex, thereby forming the mother particles. Here, on the surface of the mother particles, silica tends to more easily appear compared to titania. As a result, in the elementary profile, the region A, in which the peak intensity of titanium and the peak intensity of silicon are substantially constant, appears at the last stage of etching, and the region B, in which the peak intensity of titanium is reduced toward the particle surface while the peak intensity of silicon is increased toward the particle surface, appears immediately before the region A.
The region C is a region reflecting the elementary composition of the interlayer. In a case where the region C, that is, a region, in which the peak intensity of titanium is substantially constant and substantially no silicon is detected, exists immediately before the region B, it is determined that the silica-titania composite aerogel particles have an interlayer which is “titania layer”.
Although the region C is a region reflecting the elementary composition of a first layer, the region C does not necessarily completely coincide with the interlayer. In the region C, sometimes the side close to the region B reflects the elementary composition of the mother particles as well.
The region D is a region reflecting the elementary composition of the surface layer. In a case where the region D, that is, a region, in which the peak intensity of carbon is substantially constant and a metal element is detected as well, exists at the initial stage of etching, it is determined that the silica-titania composite aerogel particles have “layer containing the metal compound having a metal atom and a hydrocarbon group” as the surface layer.
Examples of candidates for the metal atom constituting the metal compound in the surface layer include silicon, aluminum, and titanium. Accordingly, if necessary, the identification and quantification of aluminum are performed by XPS, and an elementary profile is also created for aluminum.
Although the region D is a region reflecting the elementary composition of the surface layer, the region D does not necessarily completely coincide with a second layer. In the region D, sometimes the side close to the region C reflects the elementary composition of the first layer as well.
From the elementary profiles shown in
(Characteristics of Medium for Water Culture and the Like)
From the viewpoint of sterilizing and purifying the culture solution, the amount of the photocatalyst particles supported with respect to the medium for water culture is, for example, preferably equal to or greater than 1% by mass and equal to or smaller than 60% by mass, more preferably equal to or greater than 5% by mass and equal to or smaller than 50% by mass, and even more preferably equal to or greater than 10% by mass and equal to or smaller than 40% by mass.
By measuring the weight of the porous substance before and after supporting the photocatalyst particles, the amount of the photocatalyst particles supported is determined by the following formula.
Amount of supported photocatalyst particles with respect to porous substance (% by mass)=[(mass of porous substance after supporting photocatalyst particles−mass of porous substance before supporting photocatalyst particles)/mass of porous substance after supporting photocatalyst particles]×100
In a case where the porous substance is a fibrous material, a porous resin material, paper, or the like, by measuring the ignition loss of the medium member for water culture by using a thermogravimetric analyzer (Q50 model manufactured by TA Instruments.), the amount of the supported photocatalyst with respect to the porous substance can be determined by the following formula.
Amount of supported photocatalyst with respect to porous substance (% by mass)=[(mass of medium member for water culture heated at 400° C.)/(mass of medium member for water culture heated at 120° C.)]×100
From the viewpoint of sterilizing and purifying the culture solution, the visible light transmittance of the medium for water culture is, for example, equal to or higher than 1% and equal to or lower than 50% by mass, more preferably equal to or higher than 2% by mass and equal to or lower than 40% by mass, and even more preferably equal to or higher than 3% and equal to or lower than 20%.
In a case where the visible light transmittance of the medium for water culture is within the above range, visible light easily reaches the supported photocatalyst particles, and the culture solution is more easily sterilized and purified.
The visible light transmittance of a water purification member is measured as below.
Based on JIS K7361-1:1997, a total light transmittance (%) is measured using a haze meter (NDH-2000 manufactured by NIPPON DENSHOKU INDUSTRIES Co., LTD). The medium for water culture is cut in a thickness of 0.3±0.1 mm based on the surface to be irradiated and adjusted by means of polishing or the like, and the obtained resultant is used as a test piece.
The visible light transmittance of the medium for water culture is measured in a state where the photocatalyst particles are supported on the porous substance.
From the viewpoint of sterilizing and purifying the culture solution, a liquid absorption rate of the medium for water culture is, for example, preferably equal to or higher than 10% by mass and equal to or lower than 500% by mass, more preferably equal to or higher than 30% by mass and equal to or lower than 300% by mass, and even more preferably equal to or higher than 50% by mass and equal to or lower than 200% by mass.
In a case where the liquid absorption rate of the medium for water culture is within the above range, the probability that the germs in the culture solution to be purified and the supported photocatalyst particles will contact each other is heightened, and hence the culture solution is easily sterilized and purified.
The liquid absorption rate of the medium for water culture is measured as below.
As a sample, approximately 1 g of the medium for water culture is weighed (the weight is denoted as m1) and put into a stainless steel sieve (inner diameter 75 mm×height 20 mm) having a pore size of 1 mm.
Then, the sieve with the sample is immersed for 30 minutes in a petri dish made of glass (inner diameter 146 mm×height 28 mm) containing 300 mL of pure water (in a case where the medium for water culture is not immersed in water due to floating or the like, a fixing tool such as a mesh is used as necessary).
Thereafter, the mass of the sample after immersion is measured (the mass is denoted as m2).
Subsequently, the liquid absorption rate is calculated by the following calculation formula.
Liquid absorption rate(% by mass)=(m2−m1)/m1×100
m1=mass of sample before immersion (g)
m2=mass of sample after immersion (g)
This operation is performed 3 times, and the average thereof is adopted as the liquid absorption rate.
From the viewpoint of sterilizing and purifying the culture solution, a BET specific surface area of the medium for water culture is, for example, preferably equal to or greater than 1 m2/g and equal to or smaller than 300 m2/g, more preferably equal to or greater than 10 m2/g and equal to or smaller than 200 m2/g, and even more preferably equal to or greater than 20 m2/g and equal to or smaller than 150 m2/g.
In a case where the BET specific surface area of the medium for water culture is within the above range, the probability that the germs in the culture solution to be purified and the supported photocatalyst particles will contact each other is heightened, and hence the culture solution is easily sterilized and purified.
The BET specific surface area of the medium for water culture is measured in a state where the photocatalyst particles are supported on the porous substance. The BET specific surface area is determined by a gas adsorption method using a nitrogen gas.
From the viewpoint of sterilizing and purifying the culture solution, a ratio of the amount (kg) of the supported photocatalyst particles in the medium for water culture to the volume (L) of the culture solution held in the container of the water culture apparatus (amount of supported photocatalyst particles/volume of culture solution) is, for example, preferably equal to or higher than 0.1×10−3 kg/L and equal to or lower than 200×10−3 kg/L, more preferably equal to or higher than 0.5×10−3 kg/L and equal to or lower than 150×10−3 kg/L, and even more preferably equal to or higher than 1×10−3 kg/L and equal to or lower than 100×10−3 kg/L.
From the viewpoint of sterilizing and purifying the culture solution, a ratio of the irradiated area (m2) of the medium for water culture to the volume (L) of the culture solution held in the container of the water culture apparatus is, for example, preferably equal to or higher than 0.001 m2/L and equal to or lower than 0.6 m2/L, more preferably equal to or higher than 0.005 m2/L and equal to or lower than 0.3 m2/L, and even more preferably equal to or higher than 0.01 m2/L and equal to or lower than 0.1 m2/L.
[Manufacturing Method of Medium for Water Culture]
The manufacturing method of the medium for water culture according to the present embodiment is not particularly limited, and examples thereof include the following methods.
1) Method of coating porous substance with dispersion liquid in which photocatalyst particles are dispersed and drying the dispersion liquid such that photocatalyst particles are supported on porous substance.
In this method, because the photocatalyst particles formed of the specific titanium-based compound particles described above have a large specific surface area and a strong adhesive force, the photocatalyst particles directly adhere to the surface of the porous substance and are fixed thereto. As the coating method, known coating methods such as dip coating and spray coating may be adopted. Examples of dispersion media of the dispersion liquid to be used include volatile dispersion media such as water and various alcohols. Furthermore, a method of causing the photocatalyst particles to be supported on the porous substance by using a binder resin may also be adopted.
2) Method of using solution containing fiber and photocatalyst particles and lifting fiber out so as to obtain porous substance made of fiber and cause the photocatalyst particles to be supported on fiber surface.
3) Method of attaching photocatalyst particles to fiber (for example, by using static electricity) of porous substance made of fiber (for example, porous substance made of fiber constituted with core-sheath type composite fiber) and then performing heating.
In this method, the fiber surface is melted by heating, and the photocatalyst particles are fused and fixed to the fiber surface and supported on the porous substance.
4) Method of attaching heated photocatalyst particles (for example, by using static electricity) to porous substance made of fiber (for example, porous substance made of fiber constituted with core-sheath type composite fiber).
In this method, due to the heated photocatalyst particles, the fiber surface is melted, and the photocatalyst particles are fused and fixed to the fiber surface and supported on the porous substance.
5) Method of manufacturing porous substance by using fiber kneaded with photocatalyst particles.
In this method, for example, by using an electrostatic spinning method, fiber kneaded with photocatalyst particles is manufactured from a solution containing fiber and photocatalyst particles, and a porous substance (for example, non-woven cloth) is manufactured.
Hereinafter, embodiments of the invention will be specifically described based on examples, but the embodiments of the invention are not limited to the examples.
In the following description, unless otherwise specified, “part” is based on mass in all cases.
<Preparation of Photocatalyst Particles>
(Metatitanic Acid Particles MTA1)
Anatase seeds, that are separately prepared, are added to a titanyl sulfate solution with a TiO2 concentration of 260 g/L and a Ti3+ concentration of 6.0 g/L in terms of TiO2, in an amount of 10% by mass in terms of TiO2 with respect to TiO2 in the titanyl sulfate solution. Then, the solution is heated at a temperature equal to or higher than the boiling point thereof such that the titanyl sulfate (TiOSO4) is hydrolyzed and granular metatitanic acid is generated. Thereafter, the metatitanic acid particles are filtered and washed, then made into a slurry, and neutralized and washed at pH 7. In this way, a metatitanic acid slurry having an average primary particle diameter of 30 nm is obtained.
Subsequently, a 5 N aqueous sodium hydroxide solution is added to the metatitanic acid slurry having an average primary particle diameter of 30 nm with stirring, and the mixture is continuously stirred for 2 hours at pH 8.5, neutralized to pH 5.8 by using 6N hydrochloric acid, and filtered and washed with water. After washing, water is added thereto such that the mixture turns into a slurry again, 6N hydrochloric acid is added thereto with stirring such that pH thereof becomes 1.3, and the slurry is continuously stirred for 3 hours. From this slurry, 100 parts by mass of metatitanic acid is isolated, continuously heated at 60° C., 40 parts by mass of hexyltrimethoxysilane is added thereto with stirring, the mixture is stirred for 30 minutes, a 7N aqueous sodium hydroxide solution is then added thereto such that the mixture is neutralized to pH 7, and the mixture is filtered and washed with water. The residue obtained after filtration and washing with water is spray-dried by using a flash drier under the condition of an exit temperature of 150° C., thereby obtaining a dry powder. In an electric furnace with an oxygen concentration set to be 12% (% by volume), a heating treatment is performed on the obtained dry powder at 280° C. for 90 minutes, thereby obtaining metatitanic acid particles MTA1. The BET specific surface area of the metatitanic acid particles MTA1 is measured and found to be 220 m2/g.
(Metatitanic Acid Particles MTA2)
Metatitanic acid particles MTA2 having an average primary particle diameter of 60 nm and a BET specific surface area of 150 m2/g are obtained by the same method as that used for obtaining the metatitanic acid particles MTA1, except that the amount of the anatase seeds added is changed to 7% by mass.
(Metatitanic Acid Particles MTA3)
Metatitanic acid particles MTA3 having an average primary particle diameter of 120 nm and a BET specific surface area of 60 m2/g are obtained by the same method as that used for obtaining the metatitanic acid particles MTA1, except that the amount of the anatase seeds added is changed to 5% by mass.
(Titanium Oxide Particles TO1)
Hexyltrimethoxysilane is added dropwise to a dispersion liquid, which is obtained by dispersing commercial anatase-type titanium oxide particles (“ST-01 (manufactured by ISHIHARA SANGYO KAISHA, LTD.)”, average primary particle diameter: 8 nm) in methanol, in an amount of 40% by mass with respect to the untreated titanium oxide particles, and reacted for 1 hour at 40° C. Then, the reaction solution is spray-dried at an exit temperature of 120° C., thereby obtaining a dry powder. Thereafter, in an electric furnace with an oxygen concentration (% by volume) set to be 18%, a heating treatment is performed on the obtained dry powder at 290° C. for 1 hour, thereby obtaining titanium oxide particles TO1. The BET specific surface area of the titanium oxide particles TO1 is measured and found to be 180 m2/g.
(Titanium Oxide Particles TO2)
Octyltrimethoxysilane is added dropwise to a dispersion liquid, which is obtained by dispersing commercial anatase-type titanium oxide particles (“ST-21 (manufactured by ISHIHARA SANGYO KAISHA, LTD.)”, average primary particle diameter: 20 nm) in methanol, in an amount of 40% by mass with respect to the untreated titanium oxide particles, and reacted for 1 hour at 40° C. Then, the reaction solution is spray-dried at an exit temperature of 120° C., thereby obtaining a dry powder. Thereafter, in an electric furnace with an oxygen concentration (% by volume) set to be 20%, a heating treatment is performed on the obtained dry powder at 270° C. for 1 hour, thereby obtaining titanium oxide particles TO2. The BET specific surface area of the titanium oxide particles TO2 is measured and found to be 120 m2/g.
(Titanium Oxide Particles TO3)
Hexyltrimethoxysilane is added dropwise to a dispersion liquid, which is obtained by dispersing anatase-type titanium oxide particles prepared by a sol-gel method and having an average primary particle diameter of 160 nm in methanol, in an amount of 30% by mass with respect to the untreated titanium oxide particles, and reacted for 1 hour at 40° C. Then, the reaction solution is spray-dried at an exit temperature of 120° C., thereby obtaining a dry powder. Thereafter, in an electric furnace with an oxygen concentration (% by volume) set to be 18%, a heating treatment is performed on the obtained dry powder at 300° C. for 1 hour, thereby obtaining titanium oxide particles TO3. The BET specific surface area of the titanium oxide particles TO3 is measured and found to be 15 m2/g.
(Titanium Oxide Aerogel Particles TOAG1)
Methanol (115.4 parts) and 14.3 parts of tetrabutoxytitanium are put into a reaction container and mixed together. By using a magnetic stirrer, the mixed solution is stirred at 100 rpm, and in this state, 7.5 parts of a 0.009% by mass aqueous oxalic acid solution is added dropwise thereto for 30 seconds. The mixed solution is continuously stirred as it is for 30 minutes, thereby obtaining 137.8 parts (solid contents: 3.4 parts, liquid phase fraction: 133.9 parts) of a dispersion liquid (1).
Thereafter, 137.3 parts of the dispersion liquid (1) is put into a pressure tank and then stirred at 85 rpm, and in this state, by using a high-pressure pump, CO2 is injected into the tank. The temperature and pressure of the pressure tank are increased to 150° C. and 20 MPa respectively such that CO2 becomes in a supercritical state. While stirring is being continued, the supercritical CO2 is allowed to flow in and out, thereby removing 133 parts of the liquid phase for 60 minutes.
Subsequently, by using an entrainer pump, a mixture of 3.4 parts of isobutyltrimethoxysilane and 3.4 parts of methanol is added for 5 minutes to the solid phase remaining after the removal of the liquid phase, and the mixture is kept at 150° C./20 MPa for 30 minutes while being stirred at 85 rpm. While stirring is being continued, the supercritical CO2 is allowed to flow in and out, thereby removing 6.5 parts of the liquid phase for 30 minutes. The pressure of the tank is reduced to the atmospheric pressure for 30 minutes, thereby collecting 4.6 parts of a powder.
Thereafter, 4.0 parts of the powder is weighed and put into an SUS container, subjected to a heating treatment at 315° C. for 60 minutes in an electric furnace with an oxygen concentration (% by volume) set to be 20%, and left to cool down to 30° C. The obtained powder is sieved using a vibrating sieve having a pore size of 45 μm so as to remove coarse particles, thereby obtaining titanium oxide aerogel particles TOAG1 having an average primary particle diameter of 80 nm and a BET specific surface area of 350 m2/g.
(Silica-Titania Composite Aerogel Particles STAG1)
Methanol (115.4 parts) and 7.2 parts of tetramethoxysilane are put into a reaction container and mixed together. Furthermore, 7.2 parts of tetrabutoxytitanium is put into the container and mixed with the above components. By using a magnetic stirrer, the mixed solution is stirred at 100 rpm, and in this state, 7.5 parts of a 0.009% by mass aqueous oxalic acid solution is added dropwise thereto for 30 seconds. The mixed solution is continuously stirred as it is for 30 minutes, thereby obtaining 137.2 parts (solid contents: 4.5 parts, liquid phase fraction: 132.7 parts) of a first dispersion liquid (I-1).
Thereafter, 137.2 parts of the first dispersion liquid (I-1) is put into a pressure tank and then stirred at 85 rpm, and in this state, by using a high-pressure pump, CO2 is injected into the tank. The temperature and pressure of the pressure tank are increased to 150° C. and 20 MPa respectively such that CO2 becomes in a supercritical state. While stirring is being continued, the supercritical CO2 is allowed to flow in and out, thereby removing 132.0 parts of the liquid phase for 60 minutes.
Subsequently, by using an entrainer pump, a mixture of 4.5 parts of isobutyltrimethoxysilane and 4.5 parts of methanol is added for 5 minutes to the solid phase remaining after the removal of the liquid phase, and the mixture is kept at 150° C./20 MPa for 30 minutes while being stirred at 85 rpm. While stirring is being continued, the supercritical CO2 is allowed to flow in and out, thereby removing 8.2 parts of the liquid phase for 30 minutes. The pressure of the tank is reduced to the atmospheric pressure for 30 minutes, thereby collecting 6.0 parts of a powder.
Then, 4.0 parts of the powder is weighed and put into an SUS container and installed on a hot plate.
The powder is heated to 380° C., kept as it is for 60 minutes, and then left to cool down to 30° C. The obtained powder is sieved using a vibrating sieve having a pore size of 45 μm so as to remove coarse particles, thereby obtaining silica-titania composite aerogel particles STAG1 having an average primary particle diameter of 30 nm and a BET specific surface area of 680 m2/g.
Each of the silica-titania composite aerogel particles STAG1 is a particle having a mother particle, in which the elementary ratio Si/Ti between silicon and titanium is 3.1, and a surface layer which is present on the surface of the mother particle and contains isobutyltrimethoxysilane.
(Silica-Titania Composite Aerogel Particles STAG2)
Methanol (115.4 parts) and 7.2 parts of tetramethoxysilane are put into a reaction container and mixed together. Furthermore, 7.2 parts of tetrabutoxytitanium is put into the container and mixed with the above components. By using a magnetic stirrer, the mixed solution is stirred at 100 rpm, and in this state, 7.5 parts of a 0.009% by mass aqueous oxalic acid solution is added dropwise thereto for 30 seconds. The mixed solution is continuously stirred as it is for 30 minutes, thereby obtaining 137.2 parts (solid contents: 4.5 parts, liquid phase fraction: 132.7 parts) of a first dispersion liquid (I-1).
Thereafter, 137.2 parts of the first dispersion liquid (I-1) is put into the reaction container and stirred with a magnetic stirrer at 100 rpm. In this state, a mixed solution of 1.5 parts of tetrabutoxytitanium and 4.5 parts of butanol is added dropwise thereto for 10 minutes. The mixed solution is continuously stirred as it is for 30 minutes, thereby obtaining 143.2 parts (solid contents: 5.0 parts, liquid phase fraction: 138.2 parts) of a second dispersion liquid (II-1).
Thereafter, 143.2 parts of the second dispersion liquid (II-1) is put into a pressure tank and then stirred at 85 rpm, and in this state, by using a high-pressure pump, CO2 is injected into the tank. The temperature and pressure of the pressure tank are increased to 150° C. and 20 MPa respectively such that CO2 becomes in a supercritical state. While stirring is being continued, the supercritical CO2 is allowed to flow in and out, thereby removing 138 parts of the liquid phase for 60 minutes.
Subsequently, by using an entrainer pump, a mixture of 4.5 parts of isobutyltrimethoxysilane and 4.5 parts of methanol is added for 5 minutes to the solid phase remaining after the removal of the liquid phase, and the mixture is kept at 150° C./20 MPa for 30 minutes while being stirred at 85 rpm. While stirring is being continued, the supercritical CO2 is allowed to flow in and out, thereby removing 7.0 parts of the liquid phase for 30 minutes. The pressure of the tank is reduced to the atmospheric pressure for 30 minutes, thereby collecting 7.2 parts of a powder.
Then, 4.0 parts of the powder is weighed and put into an SUS container and installed on a hot plate. The powder is heated to 450° C., kept as it is for 60 minutes, and then left to cool down to 30° C. The obtained powder is sieved using a vibrating sieve having a pore size of 45 μm so as to remove coarse particles, thereby obtaining silica-titania composite aerogel particles STAG2 having an average primary particle diameter of 35 nm and a BET specific surface area of 480 m2/g.
Each of the silica-titania composite aerogel particles STAG2 is a particle having a mother particle, in which the elementary ratio Si/Ti between silicon and titanium is 3.1, a titania layer present on the surface of the mother particle, and a surface layer which is present on the surface of the titania layer and contains isobutyltrimethoxysilane.
For the photocatalyst particles prepared as above, the following characteristics are measured according to the method described above. The characteristics of the photocatalyst particles are summarized in Table 1.
As photocatalyst particles, 500 parts of the metatitanic acid particles MTA1 are wet with 250 parts of ethanol, and then added to and mixed with 4,250 parts of deionized water. Furthermore, 15 parts of polyvinyl alcohol and 0.15 parts of ethylene glycol diglycidyl ether are added thereto and dispersed using an ultrasonic disperser. By using 10 parts of No. 131 filter paper (manufactured by Advantech Co., Ltd., Φ600 mm) as a filter, 50 parts of the metatitanic acid particle slurry is suction-filtered such that the metatitanic acid particles in the metatitanic acid particle slurry are held in the filter paper. Then, the particles are dried at 120° C. and washed with 100 parts of deionized water such that the metatitanic acid particles are fixed into the fiber of the filter paper. In the same manner as described above, 20 sheets of No. 131 filter paper to which the metatitanic acid particles are fixed are prepared.
The No. 131 filter paper (average fiber diameter: 20 μm, average fiber length: 1.5 mm, basis weight: 200 g/m2, amount of supported photocatalyst particles: 32% by mass, BET specific surface area: 70 m2/g, thickness: 0.26 mm, hydrophilic) caused to support the metatitanic acid particles in the number of sheets shown in Table 2 and Table 3 (in Tables 2 and 3, described as number of sheets of unit member stacked, the same shall be applied to the following description) are brought into close contact with each other in the thickness direction, and fixed using a clip. Furthermore, a plurality of circular holes, which each have a diameter of 10 mm are spaced 100 mm apart from each other, are radially provided in the filter paper at an interval of 30° from the center, thereby preparing a medium for water culture.
Except that the amount of the metatitanic acid particle slurry in Example A1 is changed to 150 parts, a medium for water culture is prepared in the same manner as in Example A1 by bringing paper (basis weight: 290 g/m2, amount of photocatalyst particles supported: 52% by mass, BET specific surface area: 115 m2/g, thickness: 0.27 mm, hydrophilic) caused to support the metatitanic acid particles into close contact with each other in the thickness direction in the number of sheets shown in Table 2 and Table 3, fixing these using a clip, and radially providing a plurality of circular holes, which each have a diameter of 10 mm are spaced 100 mm apart from each other, in the paper at an interval of 30° from the center.
Except that the paper in Example A1 is changed to 10 parts of 4A paper (manufactured by advantech Co., Ltd., Φ 600 mm) and the amount of the metatitanic acid particle slurry is changed to 10 parts, a medium for water culture is prepared in the same manner as in Example A1 by bringing paper (average fiber diameter: 20 μm, average fiber length: 1.5 mm, basis weight: 105 g/m2, amount of photocatalyst particles supported: 8% by mass, BET specific surface area: 16 m2/g, thickness: 0.12 mm, hydrophilic) caused to support the metatitanic acid particles into close contact with each other in the thickness direction in the number of sheets shown in Table 2 and Table 3, fixing these using a clip, and radially providing a plurality of circular holes, which each have a diameter of 10 mm are spaced 100 mm apart from each other, in the paper at an interval of 30° from the center.
Except that the photocatalyst particles in Example A1 are changed to the metatitanic acid particles MTA2, a medium for water culture is prepared in the same manner as in Example A1 by bringing paper (basis weight: 200 g/m2, amount of photocatalyst particles supported: 30% by mass, BET specific surface area: 45 m2/g, thickness: 0.26 mm, hydrophilic) caused to support the metatitanic acid particles into close contact with each other in the thickness direction in the number of sheets shown in Table 2 and Table 3, fixing these using a clip, and radially providing a plurality of circular holes, which each have a diameter of 10 mm are spaced 100 mm apart from each other, in the paper at an interval of 30° from the center.
Except that the photocatalyst particles in Example A1 are changed to the metatitanic acid particles MTA3, a medium for water culture is prepared in the same manner as in Example A1 by bringing paper (basis weight: 220 g/m2, amount of photocatalyst particles supported: 33% by mass, BET specific surface area: 18 m2/g, thickness: 0.26 mm, hydrophilic) caused to support the metatitanic acid particles into close contact with each other in the thickness direction in the number of sheets shown in Table 2 and Table 3, fixing these using a clip, and radially providing a plurality of circular holes, which each have a diameter of 10 mm are spaced 100 mm apart from each other, in the paper at an interval of 30° from the center.
Except that the photocatalyst particles in Example A1 are changed to the metatitanic acid particles TO1, a medium for water culture is prepared in the same manner as in Example A1 by bringing paper (basis weight: 200 g/m2, amount of photocatalyst particles supported: 30% by mass, BET specific surface area: 55 m2/g, thickness: 0.26 mm, hydrophilic) caused to support the metatitanic acid particles into close contact with each other in the thickness direction in the number of sheets shown in Table 2 and Table 3, fixing these using a clip, and radially providing a plurality of circular holes, which each have a diameter of 10 mm and are spaced 100 mm apart from each other, in the paper at an interval of 30° from the center.
Except that the photocatalyst particles in Example A1 are changed to the metatitanic acid particles TO2, a medium for water culture is prepared in the same manner as in Example A1 by bringing paper caused to support the titanium oxide particles (basis weight: 190 g/m2, amount of photocatalyst particles supported: 28% by mass, BET specific surface area: 32 m2/g, thickness: 0.26 mm, hydrophilic) into close contact with each other in the thickness direction in the number of sheets shown in Table 2 and Table 3, fixing these using a clip, and radially providing a plurality of circular holes, which each have a diameter of 10 mm and are spaced 100 mm apart from each other, in the paper at an interval of 30° from the center.
Except that the photocatalyst particles in Example A1 are changed to the titanium oxide particles TO3, a medium for water culture is prepared in the same manner as in Example A1 by bringing paper (basis weight: 200 g/m2, amount of photocatalyst particles supported: 30% by mass, BET specific surface area: 5 m2/g, thickness: 0.26 mm, hydrophilic) caused to support the titanium oxide particles into close contact with each other in the thickness direction in the number of sheets shown in Table 2 and Table 3, fixing these using a clip, and radially providing a plurality of circular holes, which each have a diameter of 10 mm and are spaced 100 mm apart from each other, in the paper at an interval of 30° from the center.
As photocatalyst particles, 30 parts of the metatitanic acid particles MTA1 are heated to 200° C. and then sprayed to 100 parts of core-sheath composite non-woven cloth fiber (SOPHISTA manufactured by KURARAY CO., LTD., average fiber diameter: 14 μm, fiber length: 51 mm, basis weight: 90 g/m2, thickness: 0.12 mm) having a core portion constituted with polyethylene terephthalate (PET) and a sheath portion constituted with an ethylene-vinyl alcohol copolymer (EVOH). In this way, the photocatalyst particles are fixed to the surface of the non-woven cloth fiber formed of EVOH. In the same manner as described above, 20 sheets of non-woven cloth to which the metatitanic acid particles are fixed are prepared.
The non-woven cloth (average fiber diameter: 14 μm, average fiber length: 51 mm, basis weight: 100 g/m2, amount of photocatalyst particles supported: 10% by mass, BET specific surface area: 12 m2/g, thickness: 0.12 mm, hydrophilic) caused to support the metatitanic acid particles in the number of sheets shown in Table 2 and Table 3 are brought into close contact with each other in the thickness direction, and fixed using a clip. Furthermore, a plurality of circular holes, which each have a diameter of 10 mm and are spaced 100 mm apart from each other, are radially provided in the non-woven cloth at an interval of 30° from the center, thereby preparing a medium for water culture.
Except that the amount of the metatitanic acid particles MTA1 in Example B1 are changed to 10 parts, a medium for water culture is prepared in the same manner as in Example B1 by bringing non-woven cloth (basis weight: 93 g/m2, amount of photocatalyst particles supported: 3% by mass, BET specific surface area: 7 m2/g, thickness: 0.12 mm, hydrophilic) caused to support the metatitanic acid particles into close contact with each other in the thickness direction in the number of sheets shown in Table 2 and Table 3, fixing these using a clip, and radially providing a plurality of circular holes, which each have a diameter of 10 mm and are spaced 100 mm apart from each other, in the non-woven cloth at an interval of 30° from the center.
Except that the photocatalyst particles in Example B1 are changed to the titanium oxide aerogel particles TOAG1, a medium for water culture is prepared in the same manner as in Example B1 by bringing filter non-woven cloth (basis weight: 110 g/m2, amount of photocatalyst particles supported: 20% by mass, BET specific surface area: 68 m2/g, thickness: 0.12 mm, hydrophilic) caused to support the titanium oxide aerogel particles into close contact with each other in the thickness direction in the number of sheets shown in Table 2 and Table 3, fixing these using a clip, and radially providing a plurality of circular holes, which each have a diameter of 10 mm and are spaced 100 mm apart from each other, in the non-woven cloth at an interval of 30° from the center.
Except that the photocatalyst particles in Example B1 are changed to the silica-titania composite aerogel particles STAG1, a medium for water culture is prepared in the same manner as in Example B1 by bringing non-woven cloth (basis weight: 105 g/m2, amount of photocatalyst particles supported: 18% by mass, BET specific surface area: 120 m2/g, thickness: 0.12 mm, hydrophilic) caused to support the silica-titania composite aerogel particles into close contact with each other in the thickness direction in the number of sheets shown in Table 2 and Table 3, fixing these using a clip, and radially providing a plurality of circular holes, which each have a diameter of 10 mm and are spaced 100 mm apart from each other, in the non-woven cloth at an interval of 30° from the center.
Except that the photocatalyst particles in Example B1 are changed to the silica-titania composite aerogel particles STAG2, a medium for water culture is prepared in the same manner as in Example B1 by bringing non-woven cloth (basis weight: 112 g/m2, amount of photocatalyst particles supported: 22% by mass, BET specific surface area: 105 m2/g, thickness: 0.12 mm, hydrophilic) caused to support the silica-titania composite aerogel particles into close contact with each other in the thickness direction in the number of sheets shown in Table 2 and Table 3, fixing these using a clip, and radially providing a plurality of circular holes, which each have a diameter of 10 mm and are spaced 100 mm apart from each other, in the non-woven cloth at an interval of 30° from the center.
As photocatalyst particles, 3 parts of the metatitanic acid particles MTA1 are added to a mixed solvent of 100 parts of dichloromethane and 10 parts of N-methyl-2-pyrrolidone and dispersed using an ultrasonic disperser. Then, 4 parts of cellulose triacetate is added thereto and decomposed using the ultrasonic disperser. By using an electrospinning device, the solution is made into fiber, thereby preparing cellulose triacetate non-woven cloth fiber caused to support metatitanic acid particles. In the same manner as described above, 20 sheets of non-woven cloth to which the metatitanic acid particles are fixed are prepared.
The non-woven cloth (average fiber diameter: 10 μm, average fiber length: 38 mm, basis weight: 180 g/m2, amount of photocatalyst particles supported: 42% by mass, thickness: 0.35 mm, hydrophilic) caused to support the metatitanic acid particles in the number of sheets shown in Table 2 and Table 3 are brought into close contact with each other in the thickness direction, and fixed using a clip. Furthermore, a plurality of circular holes, which each have a diameter of 10 mm and are spaced 100 mm apart from each other, are radially provided in the non-woven cloth at an interval of 30° from the center, thereby preparing a medium for water culture.
Except that the amount of the metatitanic acid particles MTA1 in Example C1 is changed to 6 parts, a medium for water culture is prepared in the same manner as in Example C1 by bringing non-woven cloth (basis weight: 220 g/m2, amount of photocatalyst particles supported: 58% by mass, thickness: 0.28 mm, hydrophilic) caused to support the metatitanic acid particles into close contact with each other in the thickness direction in the number of sheets shown in Table 2 and Table 3, fixing these using a clip, and radially providing a plurality of circular holes, which each have a diameter of 10 mm and are spaced 100 mm apart from each other, in the non-woven cloth at an interval of 30° from the center.
Except that the amount of the metatitanic acid particles MTA1 in Example C1 is changed to 1 part, a medium for water culture is prepared in the same manner as in Example C1 by bringing non-woven cloth (basis weight: 220 g/m2, amount of photocatalyst particles supported: 18% by mass, thickness: 0.4 mm, hydrophilic) caused to support the metatitanic acid particles into close contact with each other in the thickness direction in the number of sheets shown in Table 2 and Table 3, fixing these using a clip, and radially providing a plurality of circular holes, which each have a diameter of 10 mm and are spaced 100 mm apart from each other, in the non-woven cloth at an interval of 30° from the center.
Except that the photocatalyst particles of Example C1 are changed to the metatitanic acid particles MTA2, a medium for water culture is prepared in the same manner as in Example C1 by bringing non-woven cloth (basis weight: 175 g/m2, amount of photocatalyst particles supported: 39% by mass, thickness: 0.33 mm, hydrophilic) caused to support the metatitanic acid particles into close contact with each other in the thickness direction in the number of sheets shown in Table 2 and Table 3, fixing these using a clip, and radially providing a plurality of circular holes, which each have a diameter of 10 mm and are spaced 100 mm apart from each other, in the non-woven cloth at an interval of 30° from the center.
Ethanol (200 parts), 5 parts of tetraethoxysilane, and 0.5 parts of 0.1 N hydrochloric acid are added to 20 parts of the metatitanic acid particles MTA1 as photocatalyst particles, and dispersed using an ultrasonic disperser, thereby preparing a metatitanic acid particle slurry. By using 100 parts of porous quartz glass substance (manufactured by CoorsTek KK, average pore size: 10 μm, thickness: 1 mm) as a filter, the metatitanic acid particle slurry is suction-filtered and then dried at 180° such that the metatitanic acid particles are fixed to the porous glass substance.
In this way, a medium for water culture is prepared by bringing the porous substances (average pore size: 10μ, basis weight: 400 g/m2, amount of photocatalyst particles supported: 10% by mass, thickness: 0.1 mm, hydrophilic) caused to support the metatitanic acid particles into close contact with each other in the thickness direction in the number of sheets shown in Table 2 and Table 3, fixing these by using a clip, and providing a plurality of circular holes, which each have a diameter of 10 mm and are spaced 100 mm apart from each other, in the porous substances at an interval of 30° from the center.
Except that commercial titanium oxide particles (trade name “ST-01” (manufactured by ISHIHARA SANGYO KAISHA, LTD.), average primary particle diameter: 0.012 μm, catalyst particles without a photocatalytic function expressed by visible light) are used, a medium for water culture is prepared in the same manner as in Example A1 by bringing paper (basis weight: 200 g/m2, amount of particles supported: 30% by mass, BET specific surface area: 45 m2/g, thickness: 0.25 mm, hydrophilic) caused to support the titanium oxide particles into close contact with each other in the thickness direction in the number of sheets shown in Table 2 and Table 3, fixing these using a clip, and radially providing a plurality of circular holes, which each have a diameter of 10 mm and are spaced 100 mm apart from each other, in the paper at an interval of 30° from the center.
An aluminum plate having a size of 0.23 m×0.3 m×3 mm (thickness) (provided with a plurality of holes having a diameter of 10 mm at an interval of 50 mm) obtained by supporting copper on titanium oxide is coated with a solution which is obtained by dissolving 10 parts of visible light-responsive photocatalyst particles (trade name: LUMILESH, manufactured by Showa Denko Ceramics Co., Ltd., average primary particle diameter: 150 nm) and 30 parts of a silicone resin (KR400, manufactured by Shin-Etsu Chemical Co., Ltd.) in 100 parts of ethanol and dispersing these using an ultrasonic disperser. Then, the solution is dried at 120° C., thereby preparing a medium for water culture formed of an aluminum plate (thickness of coating film: 0.1 mm) coated with copper-supporting photocatalyst particles.
<Evaluation>
(Evaluation of Characteristics)
For the obtained medium for water culture, the following characteristics are measured according to the method described above.
(Evaluation of Water Purification)
The water purification apparatus shown in
The circulation device 8 includes a transport pipe 4 transporting a culture solution stored in a storage tank 1, a transport pump 5 disposed in the middle of the route of the transport pipe, and a dripping nozzle 3 adding the culture solution transported from the transport pipe 4 dropwise to one end of the support 6.
In the water purification apparatus shown in
In this way, in the water purification apparatus shown in
By using the evaluation apparatus constituted as shown in
1) A medium for water culture is adjusted to have a size of 0.23 m (width)×0.3 m (length) and disposed on the support.
2) As a culture solution, 0.5 g of OTSUKA house No. 5 powder is dissolved in 10 L of water. As a nutrient of the culture solution, iron is adjusted to have a concentration of 2.85 ppm. Then, a certain amount of the culture solution is put into the storage tank, and 100 ml of a tomato wilt bacterial spore suspension (6.2×106 cfu/ml) is added to and mixed with the culture solution.
3) The output of the transport pump is adjusted such that a certain amount of the culture solution in the storage is supplied, and the direction of the dripping nozzle is adjusted such that the culture solution uniformly flows in the entirety of the medium for water culture on the support from the dripping nozzle.
4) The illuminance of an LED lighting Z-80PRO2-EIZO (manufactured by EIZO Corporation) is adjusted such that the illuminance becomes 20,000 lux on the surface of the medium for water culture, and the transport pipe is moved such that the culture solution is added dropwise to the surface of the medium for water culture. In this way, a test for sterilizing tomato wilt bacteria in the culture solution is started.
5) Before the start of the transport of the culture solution and 24 hours after the transport of the culture solution, the culture solution is sampled in an amount of 5 ml from the storage tank, and the water purification performance is evaluated by measuring the number of viable cells in the culture solution. Furthermore, by measuring the iron concentration in the culture solution by means of ion chromatography, the insolubilizing performance of the nutrient is evaluated.
Each evaluation is performed under the following conditions shown in Table 2 and Table 3.
The volume of the culture solution held in the storage tank equals the volume of the culture solution held in the container.
The amount of the culture solution supplied to the medium for water culture per unit time equals the amount of the culture solution supplied to the container per unit time.
—Evaluation of Water Purification Performance—
The number of viable cells in the culture solution is measured by the following dilution plate method.
From the collected culture solution sample, 0.1 ml of the solution is isolated and put into a test tube, 9.9 ml of sterilized water is added thereto and shaken, thereby preparing a 10× diluted solution. From this diluted solution, a 100× diluted solution is prepared in the same manner as described above. Furthermore, from the 100× diluted solution, a 1,000× diluted solution is prepared. Then, from the 1,000× diluted solution, 1 ml of the solution is isolated and put into a sterilized petri dish having a diameter of 9 cm, and an agar medium cooled to a temperature at which the agar medium is ready to be solidified is poured into and mixed with the solution. Thereafter, the mixture is left to stand until the mixture is solidified and then cultured for 48 hours in an incubation room kept at 35° C. The number of viable cells in the sample prepared as above is counted and multiplied by 1,000, and the obtained value is adopted as the number of viable cells.
The number of viable cells in the sample counted before the start of the culture solution transport is denoted as F1, the number of viable cells in the sample counted 24 hours after transport is denoted as F2, and the water purification performance is determined by water purification performance F=− LOG(F2/F1)×10 and evaluated based on the following evaluation standards.
A: 10≤F
B: 7≤F<10
C: 3≤F<7
D: 1≤F<3
E: F<1
—Inactivation Performance of Nutrient in Culture Solution—
The iron concentration in the culture solution is measured by ion chromatography.
The iron concentration in the sample measured before the start of the culture solution transport is denoted as D1, the iron concentration in the sample measured 24 hours after transport is denoted as D2, and the inactivation performance of the nutrient is determined by inactivation performance of nutrient D=D2/D1 and evaluated based on the following evaluation standards.
A: 0.9≤D
B: 0.8≤D<0.9
C: 0.6≤D<0.8
D: 0.4≤D<0.6
E: D<0.4
As is evident from the above results, compared to the media for water culture of comparative examples, the media for water culture according to the present examples more sterilize and purify the culture solution while further inhibiting the inactivation of the culture components in the culture solution.
The foregoing description of the exemplary embodiments of the present invention has been provided for the purposes of illustration and description. It is not intended to be exhaustive or to limit the invention to the precise forms disclosed. Obviously, many modifications and variations will be apparent to practitioners skilled in the art. The embodiments were chosen and described in order to best explain the principles of the invention and its practical applications, thereby enabling others skilled in the art to understand the invention for various embodiments and with the various modifications as are suited to the particular use contemplated. It is intended that the scope of the invention be defined by the following claims and their equivalents.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2019-048831 | Mar 2019 | JP | national |
