Patent Grant
10005045
The present invention relates to a method and device for producing a composition having a disperse phase dispersed in a continuous phase.
There are known various compositions having a disperse phase dispersed in a continuous phase, including emulsions having a disperse phase liquid dispersed in a continuous phase liquid, and microbubble compositions having a disperse phase gas dispersed in a continuous phase liquid. Conventional emulsions have been prepared by adding a liquid that is to serve as a disperse phase, together with an emulsifying agent such as a surfactant, to a liquid that is to serve as a continuous phase, to give a liquid mixture and mechanically stirring the liquid mixture to micronize the disperse phase.
As exemplary techniques for producing an emulsion more efficiently, there are disclosed in Patent Literatures 1-3 methods for causing an oil-soluble liquid and a water-soluble liquid to permeate a porous membrane. To be specific, Patent Literature 1 discloses that in order to obtain an emulsion having a small average particle size, emulsion production should be done by using a porous membrane having a small pore size and decreasing a membrane permeation rate (par. [0021]). This literature also discloses in Example 1 an example where an emulsion was produced using a porous membrane having an average pore size of 2.7 μm at a membrane permeation rate of 350 cc/3140 mm2 min. This membrane permeation rate can be converted to 6 m3/m2h.
Patent Literature 2 discloses an example where an emulsion containing 12.5% by mass of a disperse phase was produced using a porous membrane having an average pore size of 5 μm at a membrane permeation rate of 43.3 mL/25 cm2 sec (Example 12). This membrane permeation rate can be converted to 60 m3/m2h.
Patent Literature 3 discloses an example where an oil-soluble liquid and a water-soluble liquid were allowed to permeate a porous membrane having an average pore size of 5.3 μm and an effective area of 3140 mm2 at a membrane permeation rate of 2 L/min, to thereby produce an emulsion containing 40% by volume of a disperse phase (Example 3). This membrane permeation rate can be converted to 38 m3/m2h.
Non-patent Literature 1 discloses examples where emulsions each containing a disperse phase at a concentration of 1-20% by volume were produced using porous membranes having an average pore size of 7.6-20.3 μm at a membrane permeation rate of 80-240 m3/m2h (Non-patent Literature 1, FIG. 8).
The method of Patent Literature 2 is designed to produce an emulsion using a porous membrane having an average pore size of 5 μm at a membrane permeation rate of 60 m3/m2h, but the produced emulsion has only a low disperse phase content as low as 12.5% by mass. The method of Non-patent Literature 1 is designed to produce an emulsion using a porous membrane having an average pore size of 7.6-20.3 μm at a membrane permeation rate of 80-240 m3/m2h, but the produced emulsion has a low disperse phase content as low as 1-20% by volume. On the other hand, the method of Patent Literature 3 is designed to produce an emulsion containing 40% by mass of a disperse phase using a porous membrane having an average pore size of 5.3 μm, but this method uses a low membrane permeation rate as low as 38 m3/m2h. In other words, in conventional methods, it has been necessary to decrease a disperse phase content in order to achieve a relatively high membrane permeation rate, and on the contrary, to decrease a membrane permeation rate in order to achieve a relatively high disperse phase content. Thus, it has been believed in the conventional art that membrane permeation rate and disperse phase content are in trade-off relationship. This is also evident from the disclosure in Patent Literature 1 which states that in order to obtain an emulsion having a small average particle size, emulsion production should be done by using a porous membrane having a small pore size and decreasing a membrane permeation rate.
In the fields of compositions like emulsions which have a disperse phase being dispersed in a continuous phase, there has been a demand to produce a composition having a small dispersed particle size with high productivity, but it has been difficult to meet this demand in conventional methods.
In light of the aforementioned circumstances, an object of the present invention is to provide a method for producing, with high productivity, a composition having a disperse phase dispersed with a small particle size in a continuous phase.
The present inventors found that the aforementioned object can be achieved by using a porous membrane having an average pore size of not smaller than a specified value and setting a membrane permeation rate to not smaller than a specified value, and thus completed the present invention. More specifically, the aforementioned object is achieved by the present invention which is defined below.
where:
d10: a particle size when the cumulative distribution of disperse phase particles is 10%,
d90: a particle size when the cumulative distribution of disperse phase particles is 90%, and
d50: a particle size when the cumulative distribution of disperse phase particles is 50%.
a cylinder having a circumferential surface partially or wholly composed of a porous membrane, the cylinder being provided with outlets for the composition in the cross sections of both ends thereof,
a storage portion for storing a continuous phase liquid and a disperse phase fluid, the storage portion being provided on an outer periphery of the circumferential surface of the cylinder, and
a supplying means for simultaneously supplying the continuous phase liquid and the disperse phase fluid from the storage portion into the cylinder.
The present invention makes it possible to produce, with high productivity, a composition having a disperse phase dispersed with a small particle size in a continuous phase.
1. Method for Producing a Composition
The production method of the present invention comprises a permeation step at which a continuous phase liquid and a disperse phase fluid are caused to simultaneously permeate a porous membrane having an average pore size of not smaller than 5 μm at a membrane permeation rate of not lower than 50 m3/m2h. Detailed descriptions thereof are given below. As used in this invention, a numerical range expressed as “X to Y” includes the values at both ends, i.e., X and Y.
(1) Permeation
“Permeation” means that a continuous phase liquid and a disperse phase fluid are caused to pass through a membrane from one face to the other face. In the present invention, the continuous phase liquid and the disperse phase fluid are caused to simultaneously permeate a porous membrane at a membrane permeation rate of not lower than 50 m3/m2h. The term “simultaneously” means that two liquids are supplied to and caused to permeate a membrane at the same timing, and does not include a mode in which it is intentionally designed to cause one liquid to permeate earlier and the other liquid to permeate later.
The simultaneous permeation mode can be broadly classified into the following two modes: a mode in which a continuous phase liquid and a disperse phase fluid are pre-emulsified before being caused to permeate a porous membrane, and a mode in which no pre-emulsification is carried out before permeation. The “pre-emulsified” state refers to a state in which a disperse phase having an average particle size of not greater than 1 mm is dispersed in a continuous phase. In the case of no pre-emulsification, it is preferred that the flow paths of a continuous phase liquid and a disperse phase fluid from their tanks be merged together in the middle to supply them to a porous membrane in the form of a mixture thereof. The present invention can produce an intended effect even without the need for pre-emulsification, and the reason for this may be as follows. In the case of no pre-emulsification before supply of a continuous phase liquid and a disperse phase fluid to a membrane, disperse phase particles with a diameter of greater than 1 mm are supplied onto a surface of the porous membrane. In this invention, the two fluids are supplied to the membrane at a specified rate; then, it follows that said disperse phase particles receive a force greater than the Laplace pressure which depends on the pore size, due to a sufficiently high flow rate of the continuous phase liquid. As a result, the disperse phase fluid makes an entry into pores, thereby being micronized according to the mechanism described later.
In the present invention, it is necessary that the membrane permeation rate be not lower than 50 m3/m2h. The membrane permeation rate is defined as the volume of a mixed fluid permeating a membrane per unit area per unit time. As regards its lower limit, the membrane permeation rate is preferably not lower than 60 m3/m2h, greater than 200 m3/m2h, greater than 400 m3/m2h, greater than 800 m3/m2h, or greater than 1600 m3/m2h. As regards its upper limit, the membrane permeation rate is preferably not greater than 2000 m3/m2h, not greater than 1600 m3/m2h, not greater than 800 m3/m2h, or not greater than 400 m3/m2h.
The permeation step can be carried out one or more times, but in the present invention which is characterized by a high membrane permeation rate, a monodispersed composition can be obtained even after only one time of the permeation step.
(2) Porous Membrane
The porous membrane refers to a membrane having a large number of fine through-holes. As such a membrane, a known porous membrane made of glass, ceramic, nickel, or the like can be used. In the present invention, a porous membrane made of glass is preferred, and a porous membrane made of Shirasu porous glass (hereinafter also referred to as “SPG membrane”) is more preferred. The porous membrane used in this invention has an average pore size of not lower than 5 μm. Adopting a porous membrane having an average pore size of not lower than 5 μm allows a continuous phase liquid and a disperse phase fluid to permeate the porous membrane at a high rate without causing the breakage of the membrane. In this invention, these fluids are caused to permeate at a high rate; thus, even if a porous membrane with an average pore size of not lower than 5 μm is adopted, what can be produced is a composition containing a disperse phase with a smaller average particle size than said pore size. The average pore size of the porous membrane can be measured by mercury intrusion porosimetry (using an automated porosimeter).
The shape of the porous membrane is not particularly limited, and can be a disk, a flat plate, or a cylinder. However, a cylinder capable of withstanding a high membrane permeation rate is preferred. The cylinder refers to a cylindrical member whose inside is hollow. In the present invention, it is preferred that the cylinder have a circumferential surface partially or wholly composed of a porous membrane. By “have(ing) a circumferential surface partially or wholly composed of a porous membrane”, it is meant that part of the circumferential surface is composed of a porous membrane, and the remaining part thereof may be composed of other materials. Using also other materials than a porous membrane to form a cylinder makes it possible to adjust a membrane area that is effectively usable for production of the composition (hereinafter also referred to as “effective membrane area”).
The present invention can provide high productivity since a continuous phase liquid and a disperse phase fluid (hereinafter also collectively referred to as “source liquids”) are caused to permeate a porous membrane at a high rate. However, if the composition accumulates within the device, the pressure in the device may increase, leading to the breakage of the device, or an excessive pressure may be applied to the composition, causing disperse phase particles to be merged together again; thus, it may become difficult to control the particle size. Hence, in the process of production, it is preferred to avoid the accumulation of the composition within the device.
In order to suppress the accumulation of the composition, it is important to increase the discharge capacity to match the membrane permeation rate of the source liquids. In the present invention, it is preferred that the source liquids be introduced into a porous membrane from a cylinder's circumferential surface including a porous membrane portion so as to ensure that the pressure from the source liquids can be uniformly applied to the porous membrane, and that the composition be discharged from both ends of the cylinder. In this process, it is more preferred to optimize the effective membrane area and internal diameter of the cylinder to achieve a high discharge capacity. To be specific, if the longitudinal length of a porous membrane portion facing a storage portion and constituting the effective membrane area (hereinafter referred to as “effective membrane length”) is defined as L and the internal diameter of a cylinder at its ends, i.e., outlet internal diameter, is defined as d, then L/d and the membrane permeation rate F are preferred to satisfy the following relationships:
1) when 50 m3/m2h≤F≤200 m3/m2h, then 2≤L/d≤45;
2) when 200 m3/m2h<F≤400 m3/m2h, then 2≤L/d≤23;
3) when 400 m3/m2h<F≤800 m3/m2h, then 1≤L/d≤12;
4) when 800 m3/m2h<F≤1600 m3/m2h, then 1≤L/d≤6;
5) when 1600 m3/m2h<F≤2000 m3/m2h, then 1≤L/d≤4.4.
The upper limit for L/d is determined by the average linear velocity at the outlets. According to the investigation made by the present inventors, it is considered that if this average linear velocity is not greater than 5 m/sec, no such failure as described above will occur. The relationship of L/d with the membrane permeation rate F at an average linear velocity of not greater than 5 m/sec is explained below, taking as an example the case where the membrane permeation rate in 1) above is 200 m3/m2h.
In this case, the volume of the source liquids introduced into the membrane is 200 (m3/m2h)×dπL (mm2). And the total cross-sectional area of the cylinder at its ends is 2×(d/2)2π(mm2). The average linear velocity is calculated by dividing the volume of the source liquids introduced by the cylinder's total cross-sectional area at its ends. Thus, the average linear velocity is as follows:
Since the resultant value is not greater than 5 m/sec, the following relationship is satisfied:
(1/9) L/d (m/sec)≤5 m/sec,
then it follows L/d≤45.
On the other hand, the lower limit for L/d is determined by production efficiency. More specifically, in the case where the membrane permeation rate is relatively low (i.e., as low as not greater than 400 m3/m2h) like in the cases of 1) and 2) above, production efficiency will decrease if L/d is lower than 2, since the effective membrane area will also decrease. Therefore, L/d is preferably not lower than 2. On the contrary, in the case where the membrane permeation rate is relatively high (i.e., as high as greater than 400 m3/m2h) like in the cases of 3) to 5) above, sufficient production efficiency will be ensured if L/d is not lower than 1.
The dimension of the cylinder has only to satisfy the aforementioned ranges, but from the viewpoint of availability, etc., it is preferred that the cylinder have an internal diameter of 5-100 mm.
As a means for causing the source liquids to permeate, any known means can be used. For example, a pump generating only a few pulsating flows is preferred.
(3) Continuous Phase Liquid
The continuous phase liquid refers to a liquid that is to serve as a continuous phase. In the present invention, a known continuous phase liquid such as an aqueous liquid or an oily liquid can be used. The aqueous liquid refers to a liquid based on water. The oily liquid refers to a liquid based on an organic compound. The composition of this invention cannot be obtained when the continuous phase liquid and the disperse phase fluid are highly compatible with each other; thus, the continuous phase liquid is selected in consideration of its compatibility with the disperse phase fluid to be used.
The continuous phase liquid has only to be a liquid when it is supplied to a porous membrane. Thus, for example, a substance that is solid at room temperature but becomes liquid by heating can also be used as the continuous phase liquid. Alternatively, a supercooled liquid which is liquid at room temperature but solidifies with time can also be used. In consideration of workability, this step is preferably taken at room temperature (20-30° C.), so the continuous phase liquid is preferably liquid at room temperature. Such a liquid is exemplified by an inorganic substance and an organic substance. Examples of the inorganic substance include water, and examples of the organic substance include various edible oils, petroleum fuel oils, chain hydrocarbons having about 20 or less carbon atoms, and aromatic hydrocarbons having about 20 or less carbon atoms.
The continuous phase liquid may contain additives such as a surfactant, an electrolyte, and a viscosity modifier. As the surfactant, a known one can be used, and an anionic or nonionic surfactant is preferred. Since such a surfactant has no positive charge, it has an advantage in that, when a porous membrane made of glass is used, said surfactant and anions arising from silanol groups are not electrostatically attracted to each other, so that the surfactant does not experience a decrease in its activity. Examples of the anionic surfactant include carboxylates, sulfonates, and sulfuric acid ester salts such as sodium lauryl(dodecyl)sulfate. Since the anionic surfactant has ionicity, it has an advantage in that, for example, when polymer fine particles are produced as described below, it can be easily removed by washing. This surfactant is easy to wash out after beads are produced. Examples of the nonionic surfactant include glycerine fatty acid esters, sucrose fatty acid esters, polyoxyethylene alkyl ethers, and polyoxyethylene alkylphenyl ethers. The surfactant can be added in a commonly used amount, but the content of the surfactant in the continuous phase liquid is preferably in the range of 0.01 to 5% by mass, more preferably in the range of 0.02 to 2% by mass. In particular, the content of the anionic surfactant is preferably in the range of 0.1 to 5% by mass, more preferably in the range of 0.2 to 3% by mass.
Examples of the electrolyte include sodium chloride and potassium chloride. Addition of the electrolyte to the continuous phase liquid promotes the formation of an electric double layer on a porous membrane surface, thereby preventing the porous membrane from getting wet with the disperse phase fluid. In turn, the activity of the surfactant can be improved to reduce the size of disperse phase particles produced at the next step. The content of the electrolyte is preferably in the range of 0.5-5.0% by mass in the continuous phase liquid.
As the viscosity modifier, a known one can be used, and preferred examples include hydrophilic polymeric compounds such as carboxymethyl cellulose, polyvinyl alcohols, pectins, and gelatins.
(4) Disperse Phase Fluid
The disperse phase fluid refers to a liquid that is to serve as a disperse phase, and examples include aqueous liquids, oily liquids and gases. The aqueous liquid is as described above in relation to the continuous phase liquid. When an aqueous liquid is used as the disperse phase fluid, a W/O emulsion is obtained as the composition of the present invention. However, in order to finely disperse the disperse phase into the continuous phase in a porous membrane, it is necessary to avoid the porous membrane getting wet with the disperse phase fluid. Therefore, when an aqueous liquid is used as the disperse phase, a hydrophobic porous membrane is preferred, and when an oily liquid or a gas is used as the disperse phase, a hydrophilic porous membrane is preferably used. When the disperse phase fluid is liquid, it may also contain such a surfactant as mentioned above.
The oily liquid refers to, as described above, a liquid based on an organic compound. When an oily liquid is used, an O/W emulsion is obtained as the composition of the present invention. Preferred oily liquids include edible oils and fatty acid esters, but the oily liquid can be selected as appropriate depending on its application. For example, emulsions containing a fatty acid ester such as methyl laurate as a disperse phase are typically useful as cosmetic additives, food additives, or additives for coating materials.
When an oily liquid containing a polymerizable monomer is used, there can be produced an emulsion in which disperse phase particles containing a polymerizable monomer are finely dispersed with low polydispersity. This type of emulsion can be used as a starting material for suspension polymerization. The polymerizable monomer refers to a compound having a polymerizable functional group. Preferred in the present invention is a radical-polymerizable monomer with a radical-polymerizable functional group, which can be easily induced to polymerize by heating in the presence of a radical initiator. In addition, the oily liquid may contain a known coloring agent such as an organic dye, an organic pigment, an inorganic dye, or an inorganic pigment. The coloring agent is preferably a nanometer-sized particulate dispersion. The radical initiator is preferably ADVN or benzoyl peroxide, but can be selected as appropriate depending on its application.
The emulsion of the present invention comprising a polymerizable monomer as a disperse phase provides polymer particles with low polydispersity or, in other words, monodispersed polymer fine particles. Such polymer particles are useful as spacers for liquid crystal display panels, fillers for liquid chromatography separation columns, cosmetic materials, and toner materials. In particular, the composition of this invention comprising a polymerizable monomer as a disperse phase is preferred in the field of toners where polymer particles with extremely low polydispersity are needed for increasing printing resolution. Notably, this invention can produce a composition having dispersed therein a disperse phase with a smaller average particle size than the average pore size of a porous membrane; thus, even in the case of using, for example, a porous membrane having such a relatively large pore size that pores will not be clogged with a pigment, etc., a composition having dispersed therein polymer particles with a small average particle size can be obtained Hence, a composition particularly useful as a toner can be obtained.
When the disperse phase fluid is a gas, a microbubble composition having fine bubbles dispersed in the continuous phase is obtained as the composition of the present invention. In this case, the continuous phase can be an aqueous liquid or an oily liquid. Examples of the gas include air, oxygen, nitrogen, noble gas, carbon dioxide and ozone. When air or nitrogen is used as a gas, a whipped composition useful for producing aerated food products is obtained. When carbon dioxide is used as a gas, a microbubble composition useful for producing carbonated drinks is obtained. Finely dispersing an ozone-containing gas in water serving as a continuous phase is preferable not only for producing ozone water but also as a means for sterilizing water. In addition, cleaning and sterilization using this type of water are also important applications.
(5) Proportions
The proportions of the continuous phase liquid and the disperse phase fluid to be supplied are adjusted such that the disperse phase content is greater than 20% by mass. The disperse phase content is defined as the volume fraction of the disperse phase with respect to the total volume of a composition. As regards its lower limit, the disperse phase content is preferably not lower than 40% by mass, not lower than 50% by mass, or not lower than 60% by mass. As regards its upper limit, the disperse phase content is preferably not greater than 95% by mass or not greater than 80% by mass.
(6) Production of a Composite Composition
When a primary composition obtained by the present invention is used as a disperse phase fluid, a composite composition having the primary composition dispersed in a second continuous phase can be produced. To be specific, a [b]/[a]/[c] composition can be obtained by a method comprising:
the aforementioned permeation step at which a first continuous phase liquid [a] and a first disperse phase fluid [b] are caused to simultaneously permeate a porous membrane having an average pore size of not lower than 5 μm at a membrane permeation rate of not lower than 50 m3/m2h, whereby a primary composition ([b]/[a]) having dispersed therein greater than 20% by volume of the first disperse phase is prepared; and
a step at which the primary composition ([b]/[a]) and a second continuous phase liquid [c] are caused to simultaneously permeate the porous membrane having an average pore size of not lower than 5 μm at a membrane permeation rate of not lower than 50 m3/m2h, to thereby disperse greater than 20% by volume of the primary composition ([b]/[a]) as a second disperse phase.
(7) Mechanism
The mechanism for producing the effects of the present invention is not limited but may be as follows. For the sake of simplicity, the following description is made on the assumption that the disperse phase fluid is a disperse phase liquid.
The porous membrane used in the present invention is provided with curved pores that are highly uniform in cross-sectional pore area, and these pores are three-dimensionally communicated with each other while they repeatedly diverge and converge. When a continuous phase liquid and a disperse phase liquid are caused to simultaneously permeate such a porous membrane, splitting of the disperse phase liquid takes place. This splitting occurs in a highly uniform fine space; thus, the size of droplets corresponds to the pore size, and an emulsion with low polydispersity can be obtained. This phenomenon is called intra-membrane emulsification. It is believed that shearing of the liquid into droplets (ligaments) during intra-membrane emulsification mainly takes place at a junction of fine flow paths. More specifically, suppose that the two pores A and B converge at point C. The continuous phase liquid flows wetting a pore wall due to its high affinity with the wall, whereas the disperse phase liquid does not wet the pore wall due to its low affinity with the wall and flows in the state of being enclosed in the continuous phase liquid covering a pore surface. At this time, the thinly-stretched disperse phase liquid (also referred to as “disperse phase ligament”) is in contact with the continuous phase liquid via a surfactant.
Then, when the disperse phase ligaments from pores A and B flow into the junction C, the disperse phase ligaments A and B do not eliminate the surfactant molecules covering the pore surface to merge into one continuous ligament, but instead shearings of ligament A by ligament B, and of ligament B by ligament A, take place alternately while the surfactant molecules are retained on the pore surface. As a result, downstream of junction C, there are formed split ligaments D which consist of alternately arranged fragments of ligaments A and B. Thus, there may be obtained the aforementioned composition which has a small particle size, low polydispersity, and high disperse phase content.
2. Composition
(1) Disperse Phase Particle Size
The composition of the present invention is produced in the form of an O/W emulsion when using an aqueous liquid as a continuous phase liquid and an oily liquid as a disperse phase fluid, or in the form of a W/O emulsion when using an oily liquid as a continuous phase liquid and an aqueous liquid as a disperse phase fluid, or in the form of a microbubble composition when using an oily liquid or an aqueous liquid as a continuous phase liquid and a gas as a disperse phase fluid.
The particle size of disperse phase particles is determined by the laser diffraction/scattering method, and the average particle size which is defined as a median particle size (d50), a value when the cumulative volume percentage of particles is 50%, is preferably in the range of 1 to 50 μm, more preferably in the range of 1 to 30 μm.
The span (polydispersity) defined by the equation (1) mentioned below is preferably not greater than 0.6, more preferably not greater than 0.5. The lower the span is, the more preferred it is. As for its lower limit, the span is preferably not lower than 0.4, more preferably not lower than 0.3. For the purpose of the present invention, having a span of 0.3 to 0.6 is referred to as being monodispersed.
Span=(d90−d10)/d50 (1)
where:
d10: a particle size when the cumulative distribution of disperse phase particles is 10%,
d90: a particle size when the cumulative distribution of disperse phase particles is 90%, and
d50: a particle size when the cumulative distribution of disperse phase particles is 50%.
(2) Disperse Phase Content
The composition of the present invention has a disperse phase content of greater than 20% by volume. The disperse phase content is defined as the percentage by volume of a disperse phase with respect to a composition, and can be calculated by, for example, the specific gravities of a continuous phase liquid, a disperse phase fluid, and a prepared composition. A composition having a disperse phase content of greater than 20% by volume may well be said to contain a disperse phase at high concentrations, and thus is preferred as a masterbatch composition. The preferred upper and lower limits for disperse phase content are as described above.
(3) Applications
As described above, the O/W and W/O emulsion compositions of the present invention are useful as food additives, additives for coating materials, spacers for liquid crystal display panels, fillers for liquid chromatography separation columns, cosmetic materials, toner materials, and the like. Also, as described above, the microbubble composition of this invention is useful for producing whipped compositions, carbonated drinks, or ozone water.
(4) Composite Composition
As described above, when the production method of the present invention is carried out two or more times, a composite composition having a [b]/[a] composition dispersed in [c] can be obtained. In this process, it is preferable that the average particle size and span of the [b]/[a] composition serving as a final disperse phase fall within the ranges mentioned above.
3. Device
The preferred device for carrying out the production method of the present invention is a production device comprising:
a cylinder having a circumferential surface partially or wholly composed of a porous membrane, the cylinder being provided, in the cross sections of both ends thereof, with outlets for a composition having a disperse phase finely dispersed in a continuous phase,
a storage portion for storing a continuous phase liquid and a disperse phase fluid, the storage portion being provided on an outer periphery of the circumferential surface of the cylinder, and
a supplying means for simultaneously supplying the continuous phase liquid and the disperse phase fluid from the storage portion into the cylinder.
(1) Cylinder 10
The cylinder 10 and a porous membrane constituting the same are as described above. The porous membrane portion 12 refers to a portion permeated by a continuous phase liquid and a disperse phase fluid (source liquids). The other part of the cylinder besides this portion may be composed of other members, or alternatively, the porous membrane may be provided with a coating on its inner or outer wall surface to prevent the source liquids from leaking out of the cylinder. That part of the cylinder which is in contact with the outer peripheral member 40 is preferably provided with seals 50 to prevent liquid leakage. As the seal 50, a known sealing material such as O-ring can be used. The outer peripheral member 40 refers to a member disposed around the cylinder, and is preferably made of a metal such as stainless steel, ceramic, or a plastic.
In
(2) Storage Portion 20
The storage portion refers to a space for storing the source liquids. As shown in
(3) Inlet 22
The inlet 22 for introducing the source liquids is preferably formed by creating a hole in the outer peripheral member 40 as shown in
(4) Outlet 30
The cylinder 10 is preferably provided with an outlet 30 at its both ends. As described above, the device of the present invention is required to deliver high discharge capacity. Although a supplying means is omitted in
when 50 m3/m2h≤V≤200 m3/m2h, then 2≤L/d≤45;
when 200 m3/m2h<V≤400 m3/m2h, then 2≤L/d≤23;
when 400 m3/m2h<V≤800 m3/m2h, then 1≤L/d≤12;
when 800 m3/m2h<V≤1600 m3/m2h, then 1≤L/d≤6;
when 1600 m3/m2h<V≤2000 m3/m2h, then 1≤L/d≤4.4.
<Provision of a Production Device>
There was provided a cylinder 10 composed of a hydrophilic SPG membrane (10 mm in external diameter) produced by SPG Technology Co., Ltd. And as shown in
An inlet 22 with an internal diameter of 5 mm which was intended for fluid introduction was formed at two places in the longitudinally intermediate part of the outer peripheral member 40. The inlets 22 were communicated with the storage portion 20 formed between the cylinder 10 and the outer peripheral member 40. The radial length of the storage portion 20 (i.e., thickness of the storage portion) was 2 mm.
The cylinder 10 was provided with an outlet 30 at its ends, and the outer peripheral member 40 was provided with discharge inlets 42 connected to the outlets 30.
Thus, a production device 1 was provided.
<Production of a Composition>
There were provided, as a continuous phase liquid, a solution of 1.0% by mass of the nonionic surfactant Tween 20 (produced by Nacalai Tesque, Inc.) in water, and as a disperse phase liquid, liquid paraffin (produced by Nacalai Tesque, Inc.). As shown in
The results are shown in Table 1. The composition obtained using the SPG membrane with a pore size of 5 μm was an oil droplet-in-water emulsion with an average droplet size of 4.2 μm and a monodispersity index (span) of 0.48. The composition obtained using the SPG membrane with a pore size of 10 μm was an oil droplet-in-water emulsion with an average droplet size of 9.0 μm and a span of 0.47. The composition obtained using the SPG membrane with a pore size of 20 μm was an oil droplet-in-water emulsion with an average droplet size of 19.8 μm and a span of 0.52. The droplet size distributions in the emulsions were measured using a particle size distribution analyzer (SALD-200V) produced by Shimadzu Corporation.
All the emulsions had a disperse phase content of 50% by volume.
The pump used in this example was a pulsation-free double plunger pump. The plunger pump imparted little shear force to liquid feed during the suction and delivery steps, and there was no sign of micronization, etc. of oil droplets in the delivery liquid. The liquid mixture discharged from the pump had an average droplet size of 43 μm and a span of 0.52. It was found that such coarse emulsification occurred when the liquid mixture passed through the check valves installed on the suction and delivery ports of the plunger pump. Therefore, it was shown that this pump is superior as a pre-emulsification device.
There were provided the same continuous phase liquid and disperse phase liquid as in Example 1. As shown in
The results are shown in Table 1. The composition obtained using the SPG membrane with a pore size of 5 μm was an oil droplet-in-water emulsion with an average droplet size of 4.2 μm and a span of 0.51. The composition obtained using the SPG membrane with a pore size of 10 μm was an oil droplet-in-water emulsion with an average droplet size of 10.8 μm and a span of 0.53. The composition obtained using the SPG membrane with a pore size of 20 μm was an oil droplet-in-water emulsion with an average droplet size of 20 μm and a span of 0.50. All the emulsions had a disperse phase content of 25% by volume.
It was visually confirmed that the disperse phase droplets supplied to the porous membrane in this example had a diameter of about 5 mm. Since comparable emulsions to those in Example 1 were prepared in Example 2 as described above, it was demonstrated that pre-emulsification is not essential for intra-membrane emulsification.
There were provided, as a continuous phase liquid, 200 mL of a solution of 0.5% by mass Tween 20 in water, and as a disperse phase liquid, 200 mL of low-viscosity liquid paraffin (produced by Nacalai Tesque, Inc.). These liquids were pre-emulsified by stirring at 5000 rpm for 30 seconds using the homogenizer AHG-1600 produced by AS ONE Corporation. The resultant pre-emulsion had an average droplet size of 43 μm. As shown in
The results are shown in Table 1. The composition obtained using the SPG membrane with a pore size of 5 μm was an oil droplet-in-water emulsion with an average droplet size of 4.2 μm and a span of 0.43. The composition obtained using the SPG membrane with a pore size of 10 μm was an oil droplet-in-water emulsion with an average droplet size of 9.0 μm and a span of 0.45. The composition obtained using the SPG membrane with a pore size of 20 μm was an oil droplet-in-water emulsion with an average droplet size of 19.6 μm and a span of 0.48. All the emulsions had a disperse phase content of 50% by volume.
Since no significant difference was observed among the results obtained in Examples 1-3 as described above, it was confirmed that no pre-emulsification is required for emulsion in a porous membrane.
In order to determine the highest membrane permeation rate possible that allows production of a monodispersed emulsion, there were provided, as a continuous phase liquid, a solution of 1.0% by mass Tween 20 in water, and as a disperse phase liquid, low-viscosity liquid paraffin. As in Example 1, compositions were produced by the method illustrated in
The measured values shown in this table are droplet sizes (μm).
Surfactant: 1% by mass Tween 20
Further compositions were produced using, as a continuous phase liquid, a solution of 1.0% by mass of the ionic surfactant sodium lauryl(dodecyl)sulfate (produced by Nacalai Tesque, Inc.) in water, instead of the aqueous 1.0% by mass Tween 20 solution. The results are shown in Table 3.
The measured values shown in this table are droplet sizes (μm).
Surfactant: 1% by mass SDS
Patent Literature 3 (JP 2006-346565 A) discloses the results of intra-membrane emulsification by a repeated membrane permeation method with a SPG membrane 5.3 μm in average pore size, using an aqueous solution of 0.5% by mass sodium dodecyl sulfate as a continuous phase liquid, and paraffin oil as a disperse phase liquid (Patent Literature 3, Examples). The results report that emulsions obtained after 1, 20 and 50 times of membrane permeation had droplet diameters of 4.360 μm, 3.705 μm and 3.036 μm, respectively—the average droplet size decreases with the number of times of membrane permeation. In contrast to this, it is shown that the present invention enables micronization of droplets into a finer size than in the case of Patent Literature 3 after a single membrane permeation by increasing a membrane permeation rate.
The influence of the viscosity of a continuous phase liquid was investigated. As a continuous phase liquid was used a mixture obtained by adding carboxymethyl cellulose (CMC) (produced by Nacalai Tesque, Inc.) to an aqueous 0.5% Tween 20 solution to adjust the viscosity to 1, 55 or 85 mPa·s. As a disperse phase liquid, low-viscosity liquid paraffin (17 mPa·s) was used. The viscosity was measured at 21° C. using the viscometer VISCOMATE model VM-10A produced by Sekonic Corporation. The continuous phase liquid and the disperse phase liquid were supplied to a production device 1 by the method illustrated in
The results are shown in
As seen from the above, it was found that increasing the viscosity of a liquid serving as a continuous phase is effective to reduce the ratio of droplets produced to pore size.
The influence of the viscosities of a continuous phase liquid and a disperse phase liquid was investigated. As in Example 5, mixtures obtained by adding carboxymethyl cellulose (CMC) to an aqueous 0.5% by mass Tween 20 solution to adjust the viscosity (to 1, 55 or 85 mPa·s) were used as a continuous phase liquid. As a disperse phase liquid, high-viscosity liquid paraffin (250 mPa·s) (produced by Nacalai Tesque, Inc.) was used. The continuous phase liquid and the disperse phase liquid were supplied to a production device 1 by the method illustrated in
The results are shown in
Comparison between the results given in
A W/O/W composite emulsion was produced. First of all, as shown in
Next, an aqueous 1% by mass Tween 20 solution was provided as a second continuous phase liquid serving as an external aqueous phase. This liquid was fed by a supplying means 60 (a pump produced by Nihon Seimitsu Kagaku Co., Ltd.; NP-GXL 400), merged in a pipe with the water droplet-in-oil emulsion prepared above, and supplied to a production device 1′ (using, as a porous membrane, a hydrophilic SPG membrane 20 μm in average pore size, 10 mm in external diameter, and 10 mm in effective membrane length) at a membrane permeation rate of 180 m3/m2h to obtain a W/O/W composite emulsion.
The resultant emulsion had an average droplet size of 10.4 μm and a span of 0.5. As described above, introduction of emulsification in a porous membrane which requires no pre-emulsification enabled production of a monodispersed W/O/W emulsion having a disperse phase content of 50% by volume in a sequence of consecutive steps. The present invention does not require pre-emulsification of a primary emulsion and an external aqueous phase liquid, and thus makes it possible to produce a composite emulsion which is very high in active ingredient encapsulation rate, without causing the destruction of internal aqueous phase droplets.
Speaking of this composite emulsion, multiple internal aqueous phase droplets were observed in each of oil droplets for several days after the production, but these internal aqueous phase droplets coalesced into a single water droplet after a lapse of about 10 days. In other words, it was shown that a composite emulsion having a single droplet encapsulated therein was formed successfully.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2013-002664 | Jan 2013 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2014/050327 | 1/10/2014 | WO | 00 |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO2014/109385 | 7/17/2014 | WO | A |
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| 20130137782 | Shimoda | May 2013 | A1 |
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| Number | Date | Country |
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| 0 884 100 | Dec 1998 | EP |
| 2006-346565 | Dec 2006 | JP |
| 2009-297612 | Dec 2009 | JP |
| 4803508 | Oct 2011 | JP |
| WO 2008038763 | Apr 2008 | WO |
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| Number | Date | Country | |
|---|---|---|---|
| 20150343401 A1 | Dec 2015 | US |
