Composite semipermeable membrane

Abstract

Provided is a composite semipermeable membrane that exhibits excellent water generation and desalination performance even during high-pressure operation. [Solution] A composite semipermeable membrane comprising a support membrane and a separation functional layer provided on the support membrane, wherein the separation functional layer includes a thin film, and the thin film forms a pleated structure including a plurality of protrusions, and the actual length L of the thin film per 1 μm length of the support membrane in the cross-sectional direction perpendicular to the membrane surface is 3.0 μm or more, and the thickness of the thin film at the protrusions is 15 nm or more.

Description

[Technical field]

[0001] The present invention relates to a composite semipermeable membrane useful for selectively separating a liquid mixture. The composite semipermeable membrane obtained by the present invention can be suitably used, for example, for desalinizing seawater or brackish water. [Background technology]

[0002] Regarding the separation of mixtures, there are various technologies for removing substances (e.g., salts) dissolved in a solvent (e.g., water), but in recent years, the use of membrane separation methods has expanded as a process for saving energy and resources. Membranes used in membrane separation methods include microfiltration membranes, ultrafiltration membranes, nanofiltration membranes, and reverse osmosis membranes, and these membranes are used, for example, to obtain drinking water from seawater, brackish water, and water containing harmful substances, to produce ultrapure water for industrial use, to treat wastewater, and to recover valuable materials.

[0003] In particular, composite semipermeable membranes having crosslinked polyamide as a separation active layer have been proposed as reverse osmosis membranes and nanofiltration membranes. Methods for producing composite semipermeable membranes having crosslinked polyamide as a separation active layer include a method of polymerization in the presence of an organic additive (Patent Documents 1 and 2), a method of polymerization in the presence of a monofunctional acid halide (Patent Document 3), and a method of polymerization in the presence of a partially hydrolyzed acid halide (Patent Document 4). [Prior art documents] [Patent documents]

[0004] [Patent Document 1] Japanese Patent Application Publication No. 08-224452 [Patent Document 2] Japanese Patent Publication No. 6-47260 [Patent Document 3] Japan Special Publication No. 2014-521499 [Patent Document 4] Japan International Publication No. 2010 / 120326 Summary of the Invention [Problem to be solved by the invention]

[0005] Despite the various proposals mentioned above, it is difficult for conventional composite semipermeable membranes to achieve both water generation and salt rejection performance during high-pressure operation, and there is room for improvement. An object of the present invention is to provide a composite semipermeable membrane that exhibits excellent water generating properties and salt rejection properties even during high pressure operation. [Means for solving the problem]

[0006] In order to achieve the above object, the present invention has the following configuration. [1] A composite semipermeable membrane comprising a support membrane and a separation functional layer provided on the support membrane, The separation functional layer includes a thin film, the thin film forms a pleated structure including a plurality of protrusions; The actual length L of the thin film per 1 μm of the support film in a cross-sectional direction perpendicular to the film surface is 3.0 μm or more; A composite semipermeable membrane, wherein the thickness of the thin film on the protrusions is 15 nm or more. [2] The pleated structure has protrusions having a height of 200 nm or more and protrusions having a height of 10 nm or more and less than 200 nm, The ratio (N / M) of the number N of protrusions having a height of 200 nm or more to the number M of protrusions having a height of 10 nm or more is 1 / 20 or more and 1 / 2 or less. [1] The composite semipermeable membrane according to the present invention. [3] In the pleated structure, the ratio of the number of protrusions having a height of 400 nm or more to the number of protrusions is 1 / 20 or more and 1 / 5 or less. [2] The composite semipermeable membrane according to the present invention. [4] Among the protrusions, the ratio of protrusions in which the angle θ between the average line (A) of the roughness curve of the corrugated structure and the thin film and the point (a3) ​​that is equidistant from the two intersection points (a1, a2) between the thin film and the average line (A) of the roughness curve of the corrugated structure and the apex of the protrusion and the line (C) is 0<θ<75° is 5% or more. The composite semipermeable membrane according to [2] or [3]. [5] At least a portion of the plurality of protrusions has a ratio (Wa / Wb) of the maximum width Wa of the protrusion to the base width Wb of the protrusion, which is greater than 1.3, in any 10 cross sections having a length of 2.0 μm in the film surface direction of the support film. [2] to [4], the composite semipermeable membrane according to any one of the above. Effect of the Invention

[0007] According to the present invention, a composite semipermeable membrane can be obtained which exhibits excellent water generation and salt rejection performance even during high-pressure operation. [Brief description of the drawings]

[0008] [Figure 1] FIG. 1 is a cross-sectional view showing one embodiment of a composite semipermeable membrane. [Diagram 2] FIG. 2 is a cross-sectional view showing the pleated structure of the thin film in the separation functional layer. [Diagram 3] FIG. 3 is a schematic diagram showing the projection angle in the pleated structure. [Figure 4] FIG. 4 is a cross-sectional view of the pleated structure, and is a schematic diagram showing the height of the projections and the thickness of the thin film. [Diagram 5] FIG. 5 is an enlarged cross-sectional view of a protrusion in a pleated structure. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0009] Hereinafter, the embodiments of the present invention will be described in detail, but the present invention is not limited to these in any way. In this specification, "weight" and "mass", and "wt %" and "mass %" are treated as synonyms. A numerical range expressed using "~" means that the range includes the numerical values ​​before and after "~" as the lower and upper limits.

[0010] 1.Composite semipermeable membrane The composite semipermeable membrane according to this embodiment includes a support membrane and a separation functional layer provided on the support membrane. (1-1) Support membrane In this embodiment, the support membrane does not substantially have a separation function for ions, etc., and provides strength to the separation functional layer that substantially has a separation function. The size and distribution of the pores of the support membrane are not particularly limited, but for example, a support membrane having uniform and fine pores, or fine pores that gradually increase in size from the surface on which the separation functional layer is formed to the other surface, and the size of the fine pores on the surface on which the separation functional layer is formed is 0.1 nm to 100 nm, is preferable.

[0011] The material used for the support membrane and its shape are not particularly limited. For example, the support membrane may be a composite membrane having a substrate 2 and a porous support layer 3 provided on the substrate 2, as shown in FIG. 1, or it may be a membrane consisting of only one layer.

[0012] The substrate may be, for example, a fabric containing at least one material selected from polyester and aromatic polyamide as a main component. As the fabric, a long fiber nonwoven fabric or a short fiber nonwoven fabric can be preferably used.

[0013] The thickness of the substrate is preferably in the range of 10 μm or more and 200 μm or less, and more preferably in the range of 30 μm or more and 120 μm or less.

[0014] The porous support layer may contain at least one polymer selected from the group consisting of, for example, polysulfone; polyethersulfone; polyamide; polyester; cellulosic polymers such as cellulose acetate and cellulose nitrate; vinyl polymers such as polyethylene, polypropylene, polyvinyl chloride and polyacrylonitrile; homopolymers such as polyphenylene sulfide, polyphenylene sulfide sulfone, polyphenylene sulfone and polyphenylene oxide, and copolymers thereof. Among them, polysulfone, cellulose acetate, polyvinyl chloride, or a mixture thereof is preferably used for the porous support layer, and it is particularly preferable to use polysulfone which has high chemical, mechanical and thermal stability.

[0015] The thickness of the porous support layer is preferably in the range of 10 to 200 μm, more preferably in the range of 20 to 100 μm. When the thickness of the porous support layer is 10 μm or more, good pressure resistance can be obtained and a uniform support membrane without defects can be obtained, and a composite semipermeable membrane including such a porous support layer can exhibit good salt removal performance. When the thickness of the porous support layer is 200 μm or less, the amount of unreacted substances remaining during production does not increase, and a decrease in chemical resistance due to a decrease in the amount of permeated water can be prevented.

[0016] In order for the composite semipermeable membrane to have sufficient mechanical strength and packing density, the thickness of the support membrane is preferably in the range of 30 to 300 μm, and more preferably in the range of 50 to 250 μm.

[0017] The morphology of the support membrane can be observed by a scanning electron microscope, a transmission electron microscope, an atomic force microscope, etc. For example, when observing the morphology of the support membrane by a scanning electron microscope, the porous support layer is peeled off from the substrate, and then cut by freeze fracturing to obtain a sample for cross-sectional observation. This sample is thinly coated with preferably platinum, platinum-palladium, or ruthenium tetrachloride, more preferably ruthenium tetrachloride, and observed by a high-resolution field emission scanning electron microscope (UHR-FE-SEM) at an accelerating voltage of 3 to 6 kV.

[0018] The thickness of the substrate, the porous support layer, and the composite semipermeable membrane can be measured by a digital thickness gauge. In addition, since the thickness of the separation functional layer described later is very thin compared to the support membrane, the thickness of the composite semipermeable membrane can also be considered as the thickness of the support membrane. Therefore, the thickness of the composite semipermeable membrane can be measured by a digital thickness gauge, and the thickness of the porous support layer can be calculated simply by subtracting the thickness of the substrate from the thickness of the composite semipermeable membrane. When a digital thickness gauge is used, the thickness is measured at 20 points and the average value is calculated.

[0019] The thickness of the substrate, the porous support layer, and the composite semipermeable membrane may be measured by the above-mentioned microscope. The thickness is measured from an electron microscope photograph of a cross section observed at any five points for one sample, and the thickness is obtained by calculating the average value. Note that the thickness and pore size in this embodiment refer to the average value.

[0020] (1-2) Separation functional layer In the composite semipermeable membrane, it is the separation functional layer that has the substantial ability to separate ions, etc. In the cross-sectional view of the composite semipermeable membrane shown in Fig. 1, the separation functional layer is indicated by adding the reference number "4". As shown in Fig. 2, the separation functional layer has a thin film 11, and the thin film 11 forms a pleated structure including a plurality of protrusions.

[0021] The separation functional layer preferably contains polyamide as a main component. In the case of a separation functional layer mainly containing polyamide, the polyamide constituting the separation functional layer can be formed, for example, by interfacial polycondensation of a polyfunctional amine and a polyfunctional acid halide. Here, it is preferable that at least one of the polyfunctional amine and the polyfunctional acid halide contains a compound having three or more functional groups.

[0022] The thickness of the separating functional layer is usually within the range of 0.01 to 1 μm, and preferably within the range of 0.1 to 0.5 μm, in order to obtain sufficient separation performance and permeate amount.

[0023] Here, the polyfunctional amine refers to an amine having at least two primary amino groups and / or secondary amino groups in one molecule, at least one of which is a primary amino group. Examples of the polyfunctional amine include aromatic polyfunctional amines such as phenylenediamine, xylylenediamine, 1,3,5-triaminobenzene, 1,2,4-triaminobenzene, 3,5-diaminobenzoic acid, 3-aminobenzylamine, and 4-aminobenzylamine, in which two amino groups are bonded to a benzene ring at the ortho, meta, or para position, aliphatic amines such as ethylenediamine and propylenediamine, and alicyclic polyfunctional amines such as 1,2-diaminocyclohexane, 1,4-diaminocyclohexane, 4-aminopiperidine, and 4-aminoethylpiperazine.

[0024] Among them, in consideration of the selective separation property, permeability, and heat resistance of the membrane, aromatic polyfunctional amines having 2 to 4 primary amino groups and / or secondary amino groups in one molecule are preferable. As such polyfunctional aromatic amines, for example, m-phenylenediamine, p-phenylenediamine, 1,3,5-triaminobenzene, etc. are preferably used. Among them, m-phenylenediamine (hereinafter referred to as m-PDA) is more preferably used because of its easy availability and ease of handling.

[0025] These polyfunctional amines may be used alone or in combination of two or more. When using two or more simultaneously, the above amines may be combined with each other, or the above amine may be combined with an amine having at least two secondary amino groups in one molecule. Examples of the amine having at least two secondary amino groups in one molecule include piperazine and 1,3-bispiperidylpropane.

[0026] The polyfunctional acid halide refers to an acid halide having at least two halogenated carbonyl groups in one molecule. The trifunctional acid halide can be, for example, trimesic acid chloride, 1,3,5-cyclohexane tricarboxylic acid trichloride, 1,2,4-cyclobutane tricarboxylic acid trichloride, etc., and the bifunctional acid halide can be, for example, aromatic bifunctional acid halide such as biphenyl dicarboxylic acid dichloride, azobenzene dicarboxylic acid dichloride, terephthalic acid chloride, isophthalic acid chloride, naphthalenedicarboxylic acid chloride, etc., aliphatic bifunctional acid halide such as adipoyl chloride, sebacoyl chloride, etc., cyclopentane dicarboxylic acid dichloride, cyclohexane dicarboxylic acid dichloride, tetrahydrofuran dicarboxylic acid dichloride, etc., alicyclic bifunctional acid halide can be, for example,

[0027] Considering the reactivity with polyfunctional amine, the polyfunctional acid halide is preferably a polyfunctional acid chloride, and considering the selective separation property and heat resistance of the membrane, it is more preferable to use a polyfunctional aromatic acid chloride having 2 to 4 carbonyl chloride groups in one molecule. Among them, it is more preferable to use trimesoyl chloride as the polyfunctional acid halide from the viewpoint of easy availability and ease of handling. These polyfunctional acid halides may be used alone or in combination of two or more kinds.

[0028] In addition, in the separation functional layer, the thin film forms a pleated structure having multiple recesses and protrusions, as shown in Figure 2. Hereinafter, "protrusion" and "recess" refer to relatively protruding and recessed parts in the thin film, and in particular, the part above (away from the support film) the reference line A described below is called the protrusion, and the part below (towards the support film) is called the recess. A "protrusion" refers to the area from the bottom of a recess to the bottom of the adjacent recess, that is, one protrusion and the bottoms of the recesses on both sides of it. In addition, in this specification, a protrusion refers to a protrusion having a height equal to or greater than one-fifth of the 10-point average surface roughness of the thin film.

[0029] In the present embodiment, the separation functional layer has an actual thin film length L of 3.0 μm or more per 1 μm of support membrane length in the cross-sectional direction perpendicular to the membrane surface. When the actual thin film length L is 3.0 μm or more, the composite semipermeable membrane has high water permeability. The actual thin film length L is preferably 3.1 μm or more, more preferably 3.3 μm or more, and even more preferably 3.5 μm or more. In addition, the actual thin film length L is preferably 100 μm or less, and more preferably 10 μm or less. In this specification, the term "cross-sectional direction perpendicular to the film surface" means a direction perpendicular to the film surface.

[0030] The actual length L of the thin film can be determined according to a general method for determining a surface area or a specific surface area. The method is not particularly limited, but examples thereof include a method using an electron microscope such as a scanning electron microscope (SEM, FE-SEM) or a transmission electron microscope (TEM).

[0031] An example of a method for measuring the actual length L of a thin film using a transmission electron microscope (TEM) will be described. First, a sample is embedded in a water-soluble polymer to prepare an ultrathin section for TEM. The water-soluble polymer may be any polymer that can maintain the shape of the sample, such as PVA. Next, the sample is stained with OsO4 to facilitate cross-sectional observation, and cut with an ultramicrotome to prepare an ultrathin section. A cross-sectional photograph of the obtained ultrathin section is taken using an electron microscope. The observation magnification may be appropriately determined depending on the film thickness of the separation functional layer, but in order to observe the cross-sectional shape of the separation functional layer and to prevent the measurement from being localized, if the thickness of the separation functional layer is about 10 to 100 nm, the observation magnification may be set to 50,000 to 100,000 times.

[0032] For the cross-sectional photograph obtained as described above, in any 10 cross sections having a length of 2.0 μm, the actual length of the thin film per 1 μm of the support membrane in the cross-sectional direction perpendicular to the membrane surface is measured, and the arithmetic mean value is calculated as the actual length L of the thin film in the composite semipermeable membrane.

[0033] The ten-point average surface roughness of a thin film can be obtained by the following method. A cross section perpendicular to the film surface is observed using an electron microscope. The observation magnification is preferably 10,000 to 100,000 times. In the obtained cross-sectional image, the surface of the thin film (indicated by the reference symbol "11" in FIG. 2) appears as a curve, as shown in FIG. 2. A roughness curve defined based on ISO4287:1997 is obtained for this curve. The average line of the roughness curve is obtained, also based on ISO4287:1997. The average line is a straight line drawn so that the total area of ​​the region enclosed by the average line and the roughness curve is equal above and below the average line.

[0034] In the cross-sectional image with a length of 2.0 μm in the direction of the average line obtained above, as shown in FIG. 2, the average line is set as a reference line A, and for the five convex parts from the highest convex part to the fifth highest, heights from the reference line (distances from the reference line to the apex of the convex part) H1 to H5 are measured and their average value is calculated. In addition, for the five concave parts from the deepest concave part to the fifth deepest, depths (distances from the reference line to the apex of the concave part) D1 to D5 are measured and their average value is calculated. The sum of the two average values ​​obtained is the 10-point average surface roughness. The apex is the point on the convex part or concave part that is the greatest distance from the reference line.

[0035] The height of a protrusion is calculated as follows: For a protrusion that is at least one-fifth of the above-mentioned 10-point average surface roughness in a cross section 2.0 μm long in the direction of the above-mentioned average line, the sum of the average d of the depths d1 and d2 of the recesses on either side of the protrusion (the distance from the reference line to the apex of the recess) and the protrusion height h (the distance from the reference line to the apex of the protrusion) is calculated as the protrusion height Ph.

[0036] The pleated structure in this embodiment preferably has protrusions with a height of 200 nm or more and protrusions with a height of 10 nm or more and less than 200 nm. In addition, in any 10 cross sections having a length of 2.0 μm in the direction of the average line, the ratio (N / M) of the number N of protrusions having a height of 200 nm or more present on the 10 cross sections to the number M of protrusions having a height of 10 nm or more present on the 10 cross sections is preferably 1 / 20 or more and 1 / 2 or less. When N / M is 1 / 20 or more, a composite semipermeable membrane with high water permeability can be obtained. More preferably, it is 1 / 10 or more. When N / M is 1 / 2 or less, it is possible to obtain high water permeability while maintaining a high removal rate. More preferably, N / M is 1 / 3 or less.

[0037] The number of protrusions present in 10 cross sections means the total sum of the number of protrusions found in each cross section for all 10 cross sections.

[0038] In addition, in any 10 cross sections having a length of 2.0 μm in the direction of the mean line, it is preferable that all of the protrusions present in the 10 cross sections have at least one protrusion with a height of 400 nm or more. In addition, it is more preferable that the ratio (N1 / M) of the number N1 of protrusions with a height of 400 nm or more present in the 10 cross sections and the number M of protrusions with a height of 10 nm or more present in the 10 cross sections is 1 / 20 or more and 1 / 5 or less. By having protrusions with a height of 400 nm in the separation functional layer within the above range, deformation of the small protrusions is suppressed even when the composite semipermeable membrane is used under high pressure operation, so that high water permeability and salt rejection can be maintained.

[0039] As shown in Figure 3, one protrusion has two intersection points a1 and a2 between the thin film and the average line A of the roughness curve of the corrugated structure. When a line C is drawn that passes through point a3 on the average line A, which is equidistant from the intersection points a1 and a2, and the apex b of the protrusion, the angle that line C makes with the average line A that is 90° or less is called the protrusion angle. The protrusion angle is shown as θ in Figure 3.

[0040] The ratio of the number of protrusions having a protrusion angle θ of 0<θ<75° in the 10 cross sections to the total number of protrusions present in any 10 cross sections having a length of 2.0 μm in the direction of the above-mentioned average line is preferably 5% or more, more preferably 20% or more. Also, this ratio is preferably 80% or less. By having 5% of the protrusions with a protrusion angle within the above range, the protrusions overlap each other in the vertical direction, so that deformation of the protrusions can be suppressed even when the composite semipermeable membrane is used at high pressure, and as a result, it is possible to maintain high water permeability and salt rejection rate.

[0041] The thickness of the thin film at the protrusions can be measured by TEM. The preparation of ultrathin sections for TEM is as described in the description of the measurement of the actual length L. The cross section of the obtained ultrathin section is photographed by TEM. The observation magnification may be appropriately determined according to the thickness of the separation functional layer. The obtained cross section photograph can be analyzed using image analysis software.

[0042] Five protrusions are selected from the cross-sectional photograph obtained above. As shown in FIG. 4, for one protrusion, the average value d of the depths d1 and d2 from the reference line A on both sides of the convex portion to the apex of the concave portion is calculated, and the position below the reference line A (on the support membrane side) at a distance d from the reference line A is set to 0% height, and the apex of the protrusion is set to 100% height. The thickness of the thin film 11 of the protrusion is measured at 10 points within the range of 10 to 100% height. The same measurement is performed for five protrusions. The arithmetic mean value is calculated for the 50 values ​​of the thin film thickness at heights of 10 to 100% thus obtained. This value is set to the thin film thickness of the protrusion of the composite semipermeable membrane.

[0043] In this embodiment, the thickness of the thin film in the protrusions required above is 15 nm or more. When the thickness of the thin film is 15 nm or more, the composite semipermeable membrane can maintain sufficient water permeability and salt rejection rate even during high pressure operation. The thickness of the thin film in the protrusions is preferably 16 nm or more, more preferably 17 nm or more. In addition, in order to obtain excellent water permeability, the thickness of the thin film in the protrusions is preferably 30 nm or less.

[0044] In the separation functional layer of this embodiment, at least a portion of the multiple protrusions contained in the separation functional layer preferably have a ratio (Wa / Wb) of the maximum protrusion width Wa to the protrusion base width Wb of the protrusion greater than 1.3 in any 10 cross sections having a length of 2.0 μm in the membrane surface direction of the support membrane, as shown in FIG. Having protrusions with Wa / Wb greater than 1.3 provides even higher water permeability even during high pressure operation. It is more preferable that Wa / Wb is greater than 1.3 and not greater than 1.8. In this specification, the term "film surface direction" refers to a direction perpendicular to the film surface.

[0045] The maximum width Wa of the protrusions and the width Wb of the base of the protrusions can be observed by a scanning electron microscope or a transmission electron microscope. For example, if the maximum width Wa of the protrusions and the width Wb of the base of the protrusions are observed by using a scanning electron microscope, the composite semipermeable membrane sample is thinly coated with preferably platinum or platinum-palladium or ruthenium tetroxide, more preferably ruthenium tetroxide, and observed by using a high-resolution field emission scanning electron microscope (UHR-FE-SEM) at an acceleration voltage of 3 to 6 kV. As the high-resolution field emission scanning electron microscope, a Hitachi S-900 type electron microscope or the like can be used. The observation magnification is preferably 5,000 to 100,000 times.

[0046] Taking into account the magnification of the observation from the obtained electron microscope photograph, the maximum width Wa of the protrusion and the base width Wb of the protrusion can be directly measured using a scale or the like. Note that both the maximum width Wa of the protrusion and the base width of the protrusion are measured as the distance between the inner surfaces of the protrusions. The base width Wb of the protrusion is measured by drawing straight lines from the apexes of the recesses on both sides of the protrusion perpendicular to the reference line and measuring the distance between these lines.

[0047] In 10 cross sections of 2.0 μm in length in the film surface direction of the above-mentioned support film, the ratio of the number of protrusions present in the 10 cross sections having a Wa / Wb ratio of greater than 1.3 to the total number of protrusions present in the above-mentioned 10 cross sections is preferably 20% or more, and more preferably 40% or more.

[0048] 2. Manufacturing method An example of a method for producing the composite semipermeable membrane of the present embodiment described above will be described below. (2-1) Formation of separation functional layer The process of forming a separation functional layer on a support membrane will be described. In the following, an example will be given in which the support membrane has a substrate and a porous support layer. When the support membrane does not include a substrate, the "porous support layer surface" and "on the porous support layer" can be read as the "support membrane surface" and "on the support membrane", respectively.

[0049] The process of forming the separation functional layer includes a step of contacting a polyfunctional amine solution with a polyfunctional acid halide solution on the porous support layer to form a polyamide by an interfacial polycondensation reaction.

[0050] More specifically, the step of forming the separation functional layer includes: (i) contacting a porous support layer with a multifunctional amine solution; (ii) after (i), a step of contacting the porous support layer with an organic solvent solution containing a polyfunctional acid halide to produce a polyamide on the porous support layer by interfacial polycondensation. Each manufacturing step will now be described in detail.

[0051] The polyfunctional amine solution is an aqueous solution, and the polyfunctional amine concentration in this solution is preferably within the range of 0.1 to 20% by weight, more preferably within the range of 0.5 to 15% by weight. When the polyfunctional amine concentration is within the above range, a composite semipermeable membrane having sufficient salt removal performance and water permeability can be obtained.

[0052] The aqueous polyfunctional amine solution may contain a surfactant, an organic solvent, an alkaline compound, an antioxidant, and the like, so long as they do not interfere with the reaction between the polyfunctional amine and the polyfunctional acid halide.

[0053] Examples of the surfactant include compounds having a polyoxyalkylene structure, a fatty acid ester structure, or a hydroxyl group. Examples of the polyoxyalkylene structure include -(CH2CH2O)n -, -(CH2CH2(CH3)O) n -, -(CH2CH2CH2O) n -, -(CH2CH2CH2CH2O) n - and the like. Examples of the fatty acid ester structure include fatty acids having a long-chain aliphatic group. The long-chain aliphatic group may be either linear or branched, and examples of the fatty acid include stearic acid, oleic acid, lauric acid, palmitic acid, and salts thereof. Examples of fatty acid esters derived from fats and oils include beef tallow, palm oil, coconut oil, and the like. Examples of surfactants having a sulfo group include 1-hexanesulfonic acid, 1-octanesulfonic acid, 1-decanesulfonic acid, 1-dodecanesulfonic acid, perfluorobutanesulfonic acid, toluenesulfonic acid, cumenesulfonic acid, and octylbenzenesulfonic acid. Examples of surfactants having a hydroxyl group include ethylene glycol, propylene glycol, 2-propanediol, 1,4-butanediol, glycerin, sorbitol, glucose, and sucrose. The surfactant has the effect of improving the wettability of the porous support layer surface and reducing the interfacial tension between the amine aqueous solution and the nonpolar solvent.

[0054] Examples of the organic solvent include linear amide compounds and cyclic amide compounds. Examples of the linear amide compounds include N-methylformamide, N,N-dimethylformamide, N,N-dimethylacetamide, N,N-diethylformamide, and N,N-diethylacetamide. Examples of the cyclic amide compounds include N-methylpyrrolidinone, γ-butyrolactam, and ε-caprolactam. The organic solvent may act as a catalyst for the interfacial polycondensation reaction, and the addition of the organic solvent may allow the interfacial polycondensation reaction to be carried out efficiently.

[0055] Examples of alkaline compounds include alkali metal hydroxides such as sodium hydroxide and potassium hydroxide, inorganic carbonates and bicarbonates such as sodium carbonate, sodium bicarbonate, potassium carbonate and potassium bicarbonate, and organic compounds such as tetramethylammonium hydroxide and tetraethylammonium hydroxide.

[0056] Examples of the antioxidant include phenol-based antioxidants, amine-based antioxidants, sulfur-based antioxidants, and phosphorus-based antioxidants. Examples of the phenol-based antioxidants (including hindered phenol-based antioxidants) include 2,6-di-tert-butyl-4-methylphenol, 2,2'-methylenebis(4-ethyl-6-tert-butylphenol), and tetrakis-[methylene-3-(3',5'-di-tert-butyl-4'-hydroxyphenyl)propionate]methane. Examples of the amine-based antioxidants include phenyl-β-naphthylamine, α-naphthylamine, N,N'-di-sec-butyl-p-phenylenediamine, phenothiazine, and N,N'-diphenyl-p-phenylenediamine. Examples of sulfur-based antioxidants include dilauryl 3,3'-thiodipropionate, distearyl thiodipropionate, lauryl stearyl thiodipropionate, and dimyristyl 3,3'-thiodipropionate. Examples of phosphorus-based antioxidants include triphenyl phosphite, octadecyl phosphite, and trinonylphenyl phosphite. Examples of other antioxidants include ascorbic acid or an alkali metal salt thereof, sterically hindered phenolic compounds such as dibutylhydroxytoluene and butylhydroxyanisole, isopropyl citrate, dl-α-tocopherol, nordihydroguaiaretic acid, and propyl gallate.

[0057] The contact of the aqueous polyfunctional amine solution with the porous support layer is preferably carried out uniformly and continuously on the surface of the porous support layer. Specific examples of the method of contacting the aqueous polyfunctional amine solution with the porous support layer include a method of applying the aqueous polyfunctional amine solution to the porous support layer, and a method of immersing the porous support layer in the aqueous polyfunctional amine solution. The contact time between the porous support layer and the aqueous polyfunctional amine solution is preferably within a range of 1 to 10 minutes, and more preferably within a range of 1 to 3 minutes.

[0058] After the polyfunctional amine aqueous solution is brought into contact with the porous support layer, it is preferable to thoroughly drain the solution so that no droplets remain on the membrane. By thoroughly draining the solution, it is possible to prevent the remaining droplets from becoming membrane defects after membrane formation, which leads to a decrease in membrane performance. As a method for draining the solution, for example, as described in Japanese Patent Application Laid-Open No. 2-78428, a method in which the support membrane after contact with the polyfunctional amine aqueous solution is held vertically to allow excess aqueous solution to flow naturally, or a method in which an air current such as nitrogen is blown from an air nozzle to forcibly drain the solution can be used. In addition, after draining, the membrane surface can be dried to remove some of the water content of the aqueous solution.

[0059] Step (ii) will now be described. Step (ii) is a step of producing a polyamide on the porous support layer by contacting the porous support layer with an organic solvent solution containing a polyfunctional acid halide after the above step (i) through interfacial polycondensation.

[0060] The concentration of the polyfunctional acid halide in the organic solvent solution is preferably in the range of 0.01 to 10% by weight, more preferably in the range of 0.02 to 2.0% by weight. A concentration of 0.01% by weight or more can provide a sufficient reaction rate, while a concentration of 10% by weight or less can suppress the occurrence of side reactions.

[0061] The organic solvent is preferably one that is immiscible with water, dissolves the polyfunctional acid halide, and does not destroy the support film, and is inactive against the polyfunctional amine compound and the polyfunctional acid halide. Preferred examples of the organic solvent include hydrocarbon compounds such as n-hexane, n-octane, and n-decane.

[0062] The polyfunctional acid halide solution contains a compound represented by the following chemical formula (I) (hereinafter referred to as compound (I)).

[0063] [ka]

[0064] In the above formula, R1 and R2 are each independently an alkyl group having one or more carbon atoms. Compound (I) is preferably an aromatic ester, and particularly preferably a phthalate ester.Specific examples of compound (I) include dibutyl phthalate, dibutylbenzyl phthalate, diethylhexyl phthalate, diisodecyl phthalate, diisonoyl phthalate, dioctyl phthalate, diisobutyl phthalate, diethyl phthalate, dimethyl phthalate, diisooctyl phthalate, dipropyl phthalate, dicyclohexyl phthalate, dinonyl phthalate, dipentyl phthalate, dihexyl phthalate, dibenzyl phthalate, diphenyl phthalate, and bis(2-ethylhexyl) phthalate.

[0065] As a result of intensive research by the inventors, it has been found that by carrying out the formation of a separation functional layer by interfacial polycondensation of a polyfunctional amine and a polyfunctional acid halide solution in the presence of compound (I), it is possible to increase the actual length of the thin film of the separation functional layer and to increase the thickness of the thin film, thereby achieving both the water permeability and salt rejection properties of the composite semipermeable membrane.

[0066] Although the mechanism of action of compound (I) is unclear, it is believed that the interaction between the aromatic rings present in compound (I) and the aromatic rings present in the polyamide in the process of being formed is influential. In detail, in the interfacial polycondensation of a polyfunctional amine and a polyfunctional acid halide, when the amine diffuses from the polyfunctional amine aqueous solution side to the organic solvent side containing the polyfunctional acid halide, the presence of compound (I) makes the concentration gradient of the amine gentle, and as a result, the formation time of the protrusions in the separation functional layer is sufficiently long, the formation of the protrusion structure is easily promoted, and both the surface area of ​​the protrusions and the thickness of the thin film are large.

[0067] Furthermore, when forming the separation functional layer, it is preferable that the polyfunctional acid halide solution to which the compound (I) is added further contains water. Since the polyfunctional acid halide solution contains water, the concentration gradient from the polyfunctional amine aqueous solution side to the polyfunctional acid halide solution side varies in the membrane surface direction, and therefore the height and angle of the protrusions are also changed.

[0068] The concentration of compound (I) in the polyfunctional acid halide solution can be changed depending on the type of compound (I) to be added, but from the viewpoint of compatibility between water permeability and removability, it is preferably 5 ppm or more, more preferably 10 ppm or more. Also, from the viewpoint of removability, the concentration of compound (I) is preferably 500 ppm or less, more preferably 100 ppm or less.

[0069] It is also preferable to add 110 ppm or more of water to the polyfunctional acid halide solution. By containing 110 ppm or more of water in the polyfunctional acid halide solution, the water permeability can be further improved while maintaining high removability. The amount of water added to the polyfunctional acid halide solution is more preferably 120 ppm or more. In addition, from the viewpoint of removability, the amount of water added to the polyfunctional acid halide solution is preferably 300 ppm or less, more preferably 200 ppm or less.

[0070] The polyfunctional acid halide solution may further contain, as an additive, a monofunctional acid halide or trimesoyl chloride in which one acid chloride group has been hydrolyzed (hereinafter, monohydrolyzed TMC), or trimesoyl chloride in which two acid chloride groups have been hydrolyzed (hereinafter, dihydrolyzed TMC).

[0071] Examples of the monofunctional acid halide include at least one compound selected from the group consisting of benzoyl fluoride, benzoyl chloride, benzoyl bromide, methanoyl fluoride, methanoyl chloride, methanoyl bromide, ethanoyl fluoride, ethanoyl chloride, ethanoyl bromide, propanoyl fluoride, propanoyl chloride, propanoyl bromide, propenoyl fluoride, propenoyl chloride, propenoyl bromide, butanoyl fluoride, butanoyl chloride, butanoyl bromide, butenoyl fluoride, butenoyl chloride, and butenoyl bromide.

[0072] The method for contacting the organic solvent solution containing the polyfunctional acid halide with the polyfunctional amine compound solution includes, for example, coating or dropping.

[0073] In step (ii), a layer of a polyfunctional acid halide solution containing compound (I) is formed on the layer of the polyfunctional amine aqueous solution on the porous support layer obtained in step (i). Here, it is preferable that a gradient is formed in the layer of the polyfunctional acid halide solution, in which the closer to the porous support layer the greater the water content.

[0074] The above gradient is preferably formed immediately (within about 5 seconds) after the layer of the polyfunctional amine aqueous solution and the layer of the polyfunctional acid halide solution are brought into contact. The formation of the above gradient creates a surface tension difference within the layer of the polyfunctional acid halide solution, which generates a flow within the layer of the polyfunctional acid halide solution. This flow forms protrusions in the pleated structure of the separation functional layer that are narrow at the base and bulging at the body, improving water permeability.

[0075] At this time, the presence of compound (I) in the multifunctional acid halide solution allows sufficient time for the protrusions of the separation functional layer to form, while forming a flow within the layer of the multifunctional acid halide solution, i.e., the organic solvent layer, making it easier for the protrusion structure to form, and increasing both the surface area and thickness of the protrusions.

[0076] The gradient can be formed, for example, by applying a multifunctional acid halide solution having a different water content to the porous support layer multiple times. The number of applications is preferably two. The water content of the first applied multifunctional acid halide solution (first multifunctional acid halide solution) is preferably 10 to 500 ppm, more preferably 10 to 200 ppm. The water content of the second applied multifunctional acid halide solution (second multifunctional acid halide solution) is preferably 1 to 300 ppm, more preferably 1 to 150 ppm.

[0077] The temperature of the membrane surface immediately after contacting the polyfunctional amine aqueous solution with the polyfunctional acid halide solution is preferably within the range of 25 to 60°C, more preferably within the range of 30 to 50°C. By setting the membrane surface temperature at 25°C or higher, the pleated structure grows larger, improving the permeation flux. In addition, by setting the membrane surface temperature at 60°C or lower, a composite semipermeable membrane exhibiting good salt rejection properties can be obtained.

[0078] The method of applying temperature to the membrane surface may be to heat the support membrane or to contact the membrane with a heated organic solvent solution of the polyfunctional acid halide. The temperature of the membrane surface immediately after contacting the aqueous polyfunctional amine solution with the polyfunctional acid halide solution can be measured by a non-contact thermometer such as a radiation thermometer.

[0079] As described above, after the organic solvent solution of the polyfunctional acid halide is brought into contact with the aqueous polyfunctional amine solution to carry out interfacial polycondensation and the separation functional layer containing the crosslinked polyamide is formed on the porous support layer, the excess solvent may be drained off. For example, the method of draining off the liquid may be a method of holding the membrane vertically and removing the excess organic solvent by gravity. In this case, the time for holding vertically is preferably 1 to 5 minutes, more preferably 1 to 3 minutes. If this time is 1 minute or more, a sufficient amount of polyamide can be formed as the separation functional layer, and if it is 5 minutes or less, the organic solvent does not evaporate too much, and the occurrence of defects in the membrane can be suppressed.

[0080] (2-2) Formation of the support membrane The support film may be a commercially available filter. Alternatively, a support film having a substrate and a porous support layer may be formed by applying a polymer solution onto a substrate and then solidifying the polymer, or by applying a polymer solution onto a substrate such as glass, then solidifying the polymer, and peeling the polymer off from the substrate.

[0081] For example, when forming a support membrane using polysulfone, polysulfone is dissolved in N,N-dimethylformamide (hereinafter referred to as DMF) to obtain a polymer solution, which is applied to a substrate to a certain thickness and then wet-coagulated in water. This method makes it possible to obtain a porous support layer in which most of the surface has fine pores with diameters of several tens of nanometers or less.

[0082] (2-3) Other processing The composite semipermeable membrane after the separation functional layer is formed can have improved salt removal performance and water permeability by adding a process of hot water treatment at preferably 50 to 150°C, more preferably 70 to 130°C, preferably for 1 second to 10 minutes, more preferably 1 minute to 8 minutes.

[0083] In addition, the salt rejection rate can be further improved by including a step of contacting the composite semipermeable membrane with a compound (A) that reacts with a primary amino group on the separation functional layer after the hot water treatment to produce a diazonium salt or a derivative thereof, and then contacting it with a water-soluble compound (B) that is reactive with the compound (A).

[0084] Examples of the compound (A) that reacts with a primary amino group to generate a diazonium salt or a derivative thereof include aqueous solutions of nitrous acid and its salts, nitrosyl compounds, etc. Since aqueous solutions of nitrous acid and nitrosyl compounds generate gas and are easily decomposed, it is preferable to sequentially generate nitrous acid, for example, by reacting a nitrite with an acidic solution. In general, nitrite reacts with hydrogen ions to generate nitrous acid (HNO2), which can be efficiently generated when the pH of the aqueous solution is preferably 7 or less, more preferably 5 or less, and even more preferably 4 or less. Among these, an aqueous solution of sodium nitrite reacted with hydrochloric acid or sulfuric acid in an aqueous solution is particularly preferable from the viewpoint of ease of handling.

[0085] When sodium nitrite is used as the compound (A) that reacts with the primary amino group to generate a diazonium salt or a derivative thereof, the concentration of sodium nitrite is preferably in the range of 0.01 to 1% by weight. When the concentration of sodium nitrite is within the above range, a sufficient effect of generating a diazonium salt or a derivative thereof can be obtained, and the solution is easy to handle.

[0086] The temperature of the compound is preferably 15° C. to 45° C. If the temperature of the compound is within the above range, the reaction does not take too long, and the decomposition of nitrous acid is not too rapid, making the compound easy to handle.

[0087] The contact time between the primary amino group and the compound may be long enough to generate a diazonium salt and / or its derivative, and if the concentration is high, the treatment can be completed in a short time, but if the concentration is low, a long time is required. Therefore, in the solution of the above concentration, the contact time is preferably within 10 minutes, and more preferably within 3 minutes.

[0088] The method of contacting the primary amino group with the compound is not particularly limited, and the compound may be applied (coated) in a solution, or the composite semipermeable membrane may be immersed in the compound solution. Any solvent may be used to dissolve the compound, as long as the compound dissolves and the composite semipermeable membrane is not eroded. The compound solution may contain a surfactant, an acidic compound, an alkaline compound, or the like, as long as it does not interfere with the reaction between the primary amino group and the reagent.

[0089] Next, the composite semipermeable membrane in which the diazonium salt or its derivative is produced is contacted with a water-soluble compound (B) that reacts with the diazonium salt or its derivative. Examples of the water-soluble compound (B) that reacts with the diazonium salt or its derivative include chloride ions, bromide ions, cyanide ions, iodide ions, fluoroboric acid, hypophosphorous acid, sodium hydrogen sulfite, sulfite ions, aromatic amines, phenols, hydrogen sulfide, and thiocyanic acid.

[0090] When reacted with sodium hydrogen sulfite or sulfite ions, a substitution reaction occurs instantly, and amino groups are replaced with sulfo groups. In addition, when it is brought into contact with aromatic amines or phenols, a diazo coupling reaction occurs, making it possible to introduce aromatic groups onto the membrane surface.

[0091] These compounds may be used alone or in combination, or may be contacted with different compounds multiple times. The compounds to be contacted with the composite semipermeable membrane in which the diazonium salt or its derivative is formed are preferably sodium hydrogen sulfite and sulfite ion.

[0092] The concentration and time of contacting the composite semipermeable membrane formed by the diazonium salt or its derivative with the water-soluble compound (B) which reacts with the diazonium salt or its derivative can be appropriately adjusted to obtain the desired effect.

[0093] The temperature at which the composite semipermeable membrane containing the diazonium salt or its derivative is contacted with the water-soluble compound (B) that reacts with the diazonium salt or its derivative is preferably 10 to 90° C. When the contact temperature is within the above range, the reaction proceeds easily, while a decrease in the amount of permeated water due to shrinkage of the polymer does not occur.

[0094] In addition, the membrane before and after the treatment in this section (2-3) is referred to as a "composite semipermeable membrane", and the layer on the support membrane in the membrane before and after the treatment in this section (2-3) is referred to as a "separation functional layer".

[0095] (3) Use of composite separation membranes

[0096] The composite semipermeable membrane of the present embodiment thus produced is wound around a cylindrical water collection pipe having a large number of holes, together with a raw water flow path material such as a plastic net, a permeate water flow path material such as tricot, and, if necessary, a film for increasing pressure resistance, and is suitably used as a spiral-type composite semipermeable membrane element. Furthermore, this element can also be connected in series or in parallel and housed in a pressure vessel to form a composite semipermeable membrane module.

[0097] Furthermore, the above-mentioned composite semipermeable membrane and its elements and modules can be combined with a pump that supplies raw water to them, a device that pretreats the raw water, etc. to form a fluid separation device. By using this separation device, raw water can be separated into permeated water such as drinking water and concentrated water that did not permeate the composite semipermeable membrane, thereby obtaining water suitable for the purpose.

[0098] The higher the operating pressure of the fluid separation device, the higher the salt rejection rate, but the more energy required for operation is required. Also, taking into consideration the durability of the composite semipermeable membrane, the operating pressure when the treated water is passed through the composite semipermeable membrane is preferably 0.5 MPa or more and 10 MPa or less. As the supply water temperature increases, the salt rejection rate of the composite semipermeable membrane decreases, but as the temperature decreases, the membrane permeation flux also decreases, so it is preferable that the supply water temperature be 5°C or more and 45°C or less. In addition, as the supply water pH increases, there is a risk of magnesium scale formation in the case of high-salt supply water such as seawater, and there is also concern about deterioration of the composite semipermeable membrane due to high-pH operation, so operation in the neutral region is preferable.

[0099] Examples of raw water to be treated by the composite semipermeable membrane according to the present embodiment include liquid mixtures containing 50 mg / L to 100 g / L of salt (total dissolved solids), such as seawater, brackish water, and wastewater. In general, salt refers to the total dissolved solids content, and is expressed as "mass / volume" or "weight ratio." According to the definition, it can be calculated from the weight of the residue obtained by evaporating a solution filtered through a 0.45 μm filter at a temperature of 39.5 to 40.5° C., but it is more convenient to convert it from the practical salinity (S). EXAMPLES

[0100] The present invention will be described in more detail below with reference to examples, but the present invention is not limited to these examples in any way. In the examples and comparative examples, measurements were carried out as follows.

[0101] (Reference example 1) A support membrane was prepared by casting an 18 wt % solution of polysulfone in DMF onto a polyester nonwoven fabric made of long fibers at room temperature (25°C) to a thickness of 200 μm, and then immediately immersing the fabric in pure water for 5 minutes.

[0102] Example 1 The support membrane obtained in Reference Example 1 was immersed in an aqueous solution containing 4 wt% m-phenylenediamine (m-PDA) for 2 minutes, the support membrane was slowly pulled up vertically, and excess aqueous solution was removed from the support membrane surface by blowing nitrogen from an air nozzle. Next, a n-decane solution (water content 20 ppm) containing 0.12 wt% trimesoyl chloride (TMC) and 6 ppm dioctyl phthalate as an additive was applied as a first polyfunctional acid halide solution so that the support membrane surface was completely wet.

[0103] Next, the support membrane was heated in an oven at 100°C, and then, in order to remove excess solution from the support membrane, the support membrane was vertically drained and dried by blowing air at 20°C onto it using a blower.

[0104] Finally, the support membrane was washed with pure water at 90°C to obtain a composite semipermeable membrane. Tables 1 and 2 show the actual length of the thin film on the surface of the separation functional layer, the thickness of the thin film at the protrusions, the height of the protrusions (proportion), the proportion of protrusion angles θ of 0<θ<75°, the water content in the polyfunctional acid halide solution, and the membrane performance of the obtained composite semipermeable membrane.

[0105] (Examples 2 to 17) A composite semipermeable membrane was obtained in the same manner as in Example 1, except that the type of additive, the additive concentration, and the water content contained in the first polyfunctional acid halide solution were changed as shown in Table 1.

[0106] (Examples 18 to 21) A composite semipermeable membrane was obtained in the same manner as in Example 1, except that the first multifunctional acid halide solution containing the additive concentration and water content shown in Table 1 was applied so as to completely wet the support membrane surface, and then within 5 seconds, the second multifunctional acid halide solution was further applied on the layer of the first multifunctional acid halide solution so as to completely wet the surface. The second multifunctional acid halide solution was an n-decane solution containing 0.12 wt % trimesoyl chloride (TMC), and the water content and the type and concentration of additives were as shown in Table 1.

[0107] (Comparative Examples 1 to 3) A composite semipermeable membrane was obtained in the same manner as in Example 1, except that the first polyfunctional acid halide solution did not contain any additive and the water content was changed to the value shown in Table 1.

[0108] Comparative Example 4 A composite semipermeable membrane was obtained in the same manner as in Example 1, except that the additive contained in the first multifunctional acid halide solution was an aliphatic ester, and the additive concentration and water content were changed to the values ​​shown in Table 1.

[0109] (Parameter measurement of thin film in separation functional layer) The composite semipermeable membrane was embedded in polyvinyl alcohol (PVA), stained with OsO4, and cut with an ultramicrotome to prepare ultrathin sections. The obtained ultrathin sections were photographed using a transmission electron microscope. The cross-sectional photographs taken with the transmission electron microscope were imported into the image analysis software Image J. Using the methods described above, the actual length of the thin film, the thickness of the thin film at the protrusions, the height of the protrusions, and the protrusion angle were measured.

[0110] (Maximum width of protrusions in the separation functional layer (Wa), width of base of protrusions (Wb)) These parameters were measured using the method described above, and the ratio (Wa / Wb) of the maximum width of the protrusion (Wa) to the width at the base of the protrusion (Wb) was calculated. The composite semipermeable membrane sample was coated with ruthenium tetroxide, and a Hitachi S-900 type electron microscope was used as the high-resolution field emission scanning electron microscope.

[0111] (Water content in polyfunctional acid halide solution) The water content in the polyfunctional acid halide solution was measured five times using a trace water content analyzer CA-05 manufactured by Mitsubishi Chemical Industries Co., Ltd., and the average value was calculated.

[0112] (Performance evaluation under high temperature and pressure) The composite semipermeable membrane was supplied with evaluation raw water (NaCl concentration 3.2%, boron concentration approximately 5 ppm) adjusted to a temperature of 40°C and pH 6.5 at an operating pressure of 7.0 MPa, and membrane filtration was carried out for 100 hours. Thereafter, the performance of the composite semipermeable membrane was evaluated by the method described below.

[0113] (Membrane performance evaluation) (NaCl transmittance) Raw water for evaluation (NaCl concentration 3.2%, boron concentration approximately 5 ppm) adjusted to a temperature of 25°C and pH 6.5 was supplied to the composite semipermeable membrane at an operating pressure of 5.5 MPa and membrane filtration was carried out for 24 hours. The electrical conductivity of the supply water and the permeated water were then measured using a conductivity meter manufactured by Toa Denpa Kogyo Co., Ltd. to obtain the NaCl concentration of each. NaCl permeability (%) = 100 × (NaCl concentration in permeated water / NaCl concentration in feed water)

[0114] (membrane flux) In the test described above, the amount of water that passes through the membrane of the feed water (evaluation raw water) is expressed as the membrane permeation flux (m 3 / m 2 / day).

[0115] [Table 1]

[0116] [Table 2]

[0117] As shown in Table 2, the composite semipermeable membranes of Examples 1 to 21 exhibited superior salt rejection and permeability compared to Comparative Examples 1 to 4 even after high pressure operation.

[0118] Although the present invention has been described in detail and with reference to specific embodiments, it is apparent to those skilled in the art that various changes and modifications can be made without departing from the spirit and scope of the present invention. This application is based on a Japanese patent application (Patent Application No. 2021-072383) filed on April 22, 2021, the contents of which are incorporated herein by reference. [Industrial Applicability]

[0119] The composite semipermeable membrane of the present invention can be suitably used, particularly, for desalinizing seawater or brackish water.

Claims

1. A method for producing a composite semipermeable membrane having a substrate, a porous support layer, and a separation functional layer, comprising the steps of: forming the separation functional layer on the porous support layer, The step of forming the separation functional layer includes: (i) contacting the porous support layer with a m-phenylenediamine solution; (ii) after the step (i), contacting the porous support layer with an organic solvent solution containing trimesoyl chloride and the following compound (I) to produce a polyamide on the porous support layer by interfacial polycondensation; having The water content in the organic solvent solution containing trimesoyl chloride and the following compound (I) is 110 ppm or more. A method for producing a composite semipermeable membrane. 【Chemistry 1】 (In the above formula, R １ and R ２ are each independently an alkyl group having one or more carbon atoms.

2. The compound (I) is a phthalate ester. A method for producing the composite semipermeable membrane according to claim 1.

3. The compound (I) is dioctyl phthalate. A method for producing the composite semipermeable membrane according to claim 1.

4. The step (ii) comprises first applying a first organic solvent solution containing trimesoyl chloride and the compound (I) having a water content of 10 to 200 ppm to the porous support layer, and then applying a second organic solvent solution containing trimesoyl chloride and the compound (I) having a water content of 1 to 150 ppm to the porous support layer, thereby forming a layer of the organic solvent solution containing trimesoyl chloride and the compound (I) having a gradient of a water content that is greater closer to the porous support layer; the water content of the organic solvent solution containing the first trimesoyl chloride and the compound (I) is greater than the water content of the organic solvent solution containing the second trimesoyl chloride and the compound (I); A method for producing the composite semipermeable membrane according to any one of claims 1 to 3.

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