WO2010113656A1 - 複合半透膜およびその製造方法 - Google Patents
複合半透膜およびその製造方法 Download PDFInfo
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- WO2010113656A1 WO2010113656A1 PCT/JP2010/054641 JP2010054641W WO2010113656A1 WO 2010113656 A1 WO2010113656 A1 WO 2010113656A1 JP 2010054641 W JP2010054641 W JP 2010054641W WO 2010113656 A1 WO2010113656 A1 WO 2010113656A1
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- Prior art keywords
- composite semipermeable
- semipermeable membrane
- group
- membrane
- general formula
- Prior art date
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- 229920000058 polyacrylate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 1
- 229920001601 polyetherimide Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- UIIIBRHUICCMAI-UHFFFAOYSA-N prop-2-ene-1-sulfonic acid Chemical compound OS(=O)(=O)CC=C UIIIBRHUICCMAI-UHFFFAOYSA-N 0.000 description 1
- RZKYDQNMAUSEDZ-UHFFFAOYSA-N prop-2-enylphosphonic acid Chemical compound OP(O)(=O)CC=C RZKYDQNMAUSEDZ-UHFFFAOYSA-N 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 125000005504 styryl group Chemical group 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 125000000626 sulfinic acid group Chemical group 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 229910000406 trisodium phosphate Inorganic materials 0.000 description 1
- 235000019801 trisodium phosphate Nutrition 0.000 description 1
- 238000000108 ultra-filtration Methods 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- ZTWTYVWXUKTLCP-UHFFFAOYSA-N vinylphosphonic acid Chemical compound OP(O)(=O)C=C ZTWTYVWXUKTLCP-UHFFFAOYSA-N 0.000 description 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D69/00—Semi-permeable membranes for separation processes or apparatus characterised by their form, structure or properties; Manufacturing processes specially adapted therefor
- B01D69/12—Composite membranes; Ultra-thin membranes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D69/00—Semi-permeable membranes for separation processes or apparatus characterised by their form, structure or properties; Manufacturing processes specially adapted therefor
- B01D69/12—Composite membranes; Ultra-thin membranes
- B01D69/1213—Laminated layers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D67/00—Processes specially adapted for manufacturing semi-permeable membranes for separation processes or apparatus
- B01D67/0002—Organic membrane manufacture
- B01D67/0006—Organic membrane manufacture by chemical reactions
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D67/00—Processes specially adapted for manufacturing semi-permeable membranes for separation processes or apparatus
- B01D67/0081—After-treatment of organic or inorganic membranes
- B01D67/0088—Physical treatment with compounds, e.g. swelling, coating or impregnation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D67/00—Processes specially adapted for manufacturing semi-permeable membranes for separation processes or apparatus
- B01D67/0081—After-treatment of organic or inorganic membranes
- B01D67/0095—Drying
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D71/00—Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
- B01D71/06—Organic material
- B01D71/70—Polymers having silicon in the main chain, with or without sulfur, nitrogen, oxygen or carbon only
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D71/00—Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
- B01D71/06—Organic material
- B01D71/76—Macromolecular material not specifically provided for in a single one of groups B01D71/08 - B01D71/74
- B01D71/82—Macromolecular material not specifically provided for in a single one of groups B01D71/08 - B01D71/74 characterised by the presence of specified groups, e.g. introduced by chemical after-treatment
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/44—Treatment of water, waste water, or sewage by dialysis, osmosis or reverse osmosis
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/44—Treatment of water, waste water, or sewage by dialysis, osmosis or reverse osmosis
- C02F1/441—Treatment of water, waste water, or sewage by dialysis, osmosis or reverse osmosis by reverse osmosis
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D183/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers
- C09D183/04—Polysiloxanes
- C09D183/08—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen, and oxygen
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2323/00—Details relating to membrane preparation
- B01D2323/02—Hydrophilization
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2323/00—Details relating to membrane preparation
- B01D2323/34—Use of radiation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2323/00—Details relating to membrane preparation
- B01D2323/34—Use of radiation
- B01D2323/345—UV-treatment
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2323/00—Details relating to membrane preparation
- B01D2323/40—Details relating to membrane preparation in-situ membrane formation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2325/00—Details relating to properties of membranes
- B01D2325/02—Details relating to pores or porosity of the membranes
- B01D2325/027—Nonporous membranes
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2103/00—Nature of the water, waste water, sewage or sludge to be treated
- C02F2103/08—Seawater, e.g. for desalination
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F212/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
- C08F212/02—Monomers containing only one unsaturated aliphatic radical
- C08F212/04—Monomers containing only one unsaturated aliphatic radical containing one ring
- C08F212/14—Monomers containing only one unsaturated aliphatic radical containing one ring substituted by heteroatoms or groups containing heteroatoms
- C08F212/30—Sulfur
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/22—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
- C08G77/26—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen nitrogen-containing groups
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A20/00—Water conservation; Efficient water supply; Efficient water use
- Y02A20/124—Water desalination
- Y02A20/131—Reverse-osmosis
Definitions
- the present invention relates to a composite semipermeable membrane for selectively separating components of a liquid mixture and a method for producing the same. Specifically, the present invention relates to a composite semipermeable membrane comprising a separation functional layer and a porous support for supporting the separation functional layer and having excellent selective permeability.
- membrane separation methods have been actively used in the water treatment field as a low-cost process for saving energy and resources.
- Typical membranes used in membrane separation methods include microfiltration membranes, ultrafiltration membranes, nanofiltration membranes (NF membranes), and reverse osmosis membranes (RO membranes).
- RO membranes and NF membranes are composite semipermeable membranes, most of which have a thin layer (separation functional layer) obtained by crosslinking a gel layer and a polymer on a microporous support membrane, and a microporous
- a thin layer obtained by crosslinking a gel layer and a polymer on a microporous support membrane
- a microporous One of those having a thin film layer (separation function layer) obtained by polycondensing monomers on a support membrane, and a crosslinked polyamide is frequently used as a material for these thin film layers.
- Semipermeable membranes are widely used by being applied to reverse osmosis membranes and NF membranes because the water permeability and the salt removal rate are likely to be high.
- an object of the present invention is to provide a composite semipermeable membrane excellent in selective separation of divalent ions with respect to monovalent ions and a method for producing the same.
- the present invention has the following configuration.
- a composite semipermeable membrane comprising: a condensation product obtained from the above, and a polymer conjugated base having at least one acidic group.
- n represents an integer of 1 to 4, and R 1 and R 2 represent a hydrogen atom or an alkyl group having 1 to 4 carbon atoms.
- the polymer conjugate base is obtained by polymerizing a monomer or monomer mixture containing at least one conjugate base of a compound having at least one polymerizable double bond. Or the composite semipermeable membrane according to (II).
- a coating liquid comprising a compound represented by the general formula (2) and a monomer or a monomer mixture containing at least one compound having an acidic group and at least one polymerizable double bond.
- a method for producing a composite semipermeable membrane comprising a step of forming a separation functional layer by coating on a microporous support membrane, irradiating with energy rays, and then drying by heating.
- n is an integer of 1 to 4
- R 1 and R 2 are a hydrogen atom or an alkyl group having 1 to 4 carbon atoms
- Y ⁇ is an arbitrary anion.
- a composite semipermeable membrane excellent in selective separation of divalent ions with respect to monovalent ions can be obtained.
- the composite semipermeable membrane of the present invention has superior selective separation, so it is economically superior to conventional composite semipermeable membranes, and the chlorine-containing raw water is permeated continuously or intermittently to sterilize the membrane. Even if it goes, it does not deteriorate as the conventional composite semipermeable membrane.
- a separation functional layer having substantially separation performance is coated on a microporous support membrane having substantially no separation performance.
- the material used for the microporous support membrane and its shape are not particularly limited, but it is usually composed of a porous support formed on a base material, for example, at least one selected from polyester or aromatic polyamide as a main component Polysulfone, cellulose acetate, polyvinyl chloride, or a mixture thereof (porous support) reinforced with a fabric (base material) is preferably used.
- a material used as the porous support it is particularly preferable to use polysulfone having high chemical, mechanical and thermal stability.
- the thickness of the above-mentioned microporous support membrane affects the strength of the composite semipermeable membrane and the packing density when it is used as an element. In order to obtain sufficient mechanical strength and packing density, it is preferably in the range of 50 to 300 ⁇ m, more preferably in the range of 100 to 250 ⁇ m.
- the thickness of the porous support in the microporous support membrane is preferably in the range of 10 to 200 ⁇ m, more preferably in the range of 30 to 100 ⁇ m.
- the form of the porous support can be observed with a scanning electron microscope, a transmission electron microscope, or an atomic microscope.
- a scanning electron microscope the porous support is peeled off from the substrate, and then cut by a freeze cleaving method to obtain a sample for cross-sectional observation.
- the sample is thinly coated with platinum, platinum-palladium or ruthenium tetrachloride, preferably ruthenium tetrachloride, and observed with a high-resolution field emission scanning electron microscope (UHR-FE-SEM) at an acceleration voltage of 3 to 6 kV.
- UHR-FE-SEM high-resolution field emission scanning electron microscope
- Hitachi S-900 electron microscope can be used as the high-resolution field emission scanning electron microscope.
- the film thickness and surface pore diameter of the porous support are determined from the obtained electron micrograph.
- the thickness and the hole diameter in the present invention mean an average value when measured five times.
- the separation functional layer is a layer substantially having separation performance, and is a condensation product formed by condensation of at least one selected from the ion group represented by the general formula (1). And a high molecular conjugate base having at least one acidic group.
- this separation functional layer it is considered that the desired effect can be obtained by the present invention because the conjugate base of the acidic group is ionically bonded to the imidazolium group of the condensation product.
- the method for producing the separation functional layer is not particularly limited.
- a production method including a step of forming a separation functional layer by applying a coating liquid containing a compound represented by (2) onto a microporous support membrane, irradiating energy rays, and then drying by heating are preferably employed.
- the method for applying the coating liquid on the microporous support film is not particularly limited, and it can be applied by various known methods such as dip coating, spin coating, spray coating, and brush coating.
- the film is allowed to stand by being covered with a film such as a polyester film whose degree of polymerization does not change by contact with a solvent. preferable. This is because the necessary amount of coating liquid is reduced and the operation is simple.
- the standing time is preferably 30 seconds to 2 minutes. Further, after peeling off the film, it is desirable to sufficiently drain the liquid so that no droplets remain on the film.
- a method for draining a method of forcibly draining by blowing air such as nitrogen from an air nozzle can be used.
- the composite semipermeable membrane of the present invention is obtained by applying the coating liquid onto the microporous support membrane, irradiating with energy rays, and then drying by heating.
- the conjugate base of a monomer or monomer mixture containing at least one compound having an acidic group and at least one polymerizable double bond is polymerized by irradiation with energy rays.
- the irradiation time of the energy beam is 5 seconds to 15 minutes.
- at least 1 sort (s) chosen from the ion group represented by the said General formula (1) is condensed by heat drying, and a condensation product is obtained, but heat drying temperature is 40 degreeC or more.
- the heat drying time is preferably 10 minutes or longer. If the heating and drying temperature is less than 40 ° C. or the heating time is less than 10 minutes, the condensation reaction of ions of the silicon compound represented by the above general formula (1) does not proceed sufficiently, a defect is produced, and the film performance is lowered. .
- the composite semipermeable membrane obtained by the above production method is preferably hydrophilized by immersing in an aqueous solution of alcohol for 1 to 20 minutes. This is because alcohol is soluble in water and easily compatible with the hydrophobic membrane surface, so that the membrane surface can be hydrophilized and the amount of membrane water can be increased. As alcohol used for hydrophilization, it is common to use 10 wt% isopropyl alcohol aqueous solution.
- Examples of the acidic group in the present invention include, but are not limited to, a sulfonic acid group, a sulfinic acid group, a carboxyl group, a phosphonic acid group, a phosphinic acid group, a hydroxyl group, and a thiol group.
- a sulfonic acid group a sulfinic acid group
- a carboxyl group a phosphonic acid group
- a phosphinic acid group a hydroxyl group
- a thiol group examples of the acidic group in the present invention.
- at least one selected from a carboxyl group, a sulfonic acid group, and a phosphonic acid group is preferable from the viewpoint of acidity and availability of the reagent.
- conjugated base of the polymer having at least one acidic group in the present invention examples include conjugated bases such as polyamide, polyester, polycarbonate, polyacrylate, polyurethane, polyether, and polyimide having an acidic group in a part of the repeating unit. These may be either homopolymers or copolymers, and are not particularly limited as long as they are ion-bonded to the imidazolium group in the ion condensation product represented by the general formula (1).
- the polymer conjugate base is obtained by polymerizing a monomer or monomer mixture containing at least one conjugate base of a compound having at least one polymerizable double bond. Preferably there is.
- examples of the polymerizable double bond in the present invention include (meth) acryloyl group, (meth) acryloyloxy group, (meth) acrylamide group, allyl group, vinyl group, styryl group and the like. Is not to be done.
- examples of the compound having an acidic group and one or more polymerizable double bonds include vinyl sulfonic acid and its salt, allyl sulfonic acid, o-styrene sulfonic acid and its salt, p- Styrenesulfonic acid and its salt, m-styrenesulfonic acid and its salt, 2-vinylbenzoic acid and its salt, 3-vinylbenzoic acid and its salt, 4-vinylbenzoic acid and its salt, acrylic acid and its salt, methacrylic acid Acids and salts thereof, 2-acryloyloxyethyl succinic acid, 2-methacryloyloxyethyl succinic acid, 3,5-diacrylamide benzoic acid, vinylphosphonic acid, allylphosphonic acid, o-styrenephosphonic acid and salts thereof, p -Styrene phosphonic acid and its salt, m-styrene phosphonic acid and its salt, and the
- the ion represented by the general formula (1) is preferably a compound in which n is 3, and R 1 and R 2 are methyl groups.
- the acidic group possessed by the polymer present in the thin film is preferably at least one selected from a carboxylic acid group, a sulfonic acid group, and a phosphonic acid group.
- the content of the ion represented by the general formula (1) in the coating liquid is preferably about 10 to 90% by weight in the reactive tissue, and 10 to 50% by weight. % Is more preferable.
- the polymer having an acidic group present in the separation functional layer is eluted.
- Such a change is caused by the absorption band (1010 cm ⁇ 1) derived from the Si—O—Si stretching vibration of the intensity of the absorption band derived from the acidic group in the infrared absorption spectrum measured by the reflection type infrared absorption spectrum measuring apparatus. This can be confirmed from the decrease in the ratio of the strength to In the above operation, when the same operation as described above is performed except that pure water is used instead of 1 mol / L hydrochloric acid, the intensity ratio does not change.
- the solvent used in the coating solution any solvent that does not dissolve the microporous support membrane and is miscible with water can be used without particular limitation.
- the coating solution contains equimolar or more water with respect to the number of functional groups that can be condensed in the ion group represented by the general formula (1) having an imidazolium group. It is preferable.
- the monomer or monomer mixture in the present invention is not particularly limited as long as it contains at least one compound containing at least one polymerizable double bond.
- two or more kinds of compounds containing one or more polymerizable double bonds may be contained, and a polymerization initiator and a polymerization aid may be used as long as the effects of the present invention are not impaired. Other additives may be included.
- the polymerization initiator and the polymerization accelerator are not particularly limited, and are appropriately selected according to the structure of the compound containing one or more polymerizable double bonds, the polymerization technique, and the like.
- any known one can be used without particular limitation as long as it is soluble in the solvent used.
- the concentration of the polymerization initiator to be added is 5% by weight in the reactive composition. The following is preferable.
- the composite semipermeable membrane of the present invention formed in this way has a large number of pores together with a raw water channel material such as a plastic net, a permeate channel material such as tricot, and a film for increasing pressure resistance if necessary. Is wound around a cylindrical water collecting pipe and is suitably used as a spiral composite semipermeable membrane element. Furthermore, a composite semipermeable membrane module in which these elements are connected in series or in parallel and accommodated in a pressure vessel can be obtained.
- the above-described composite semipermeable membrane, its elements, and modules can be combined with a pump for supplying raw water to them, a device for pretreating the raw water, and the like to constitute a fluid separation device.
- a separation device By using this separation device, permeated water such as drinking water and concentrated water that has not permeated through the membrane can be separated from raw water to obtain water suitable for the purpose, and can be expected to be used in industrial applications. .
- Example 4 A composite semipermeable membrane in the same manner as in Example 1 except that 3-methyl-1- (3-trimethoxysilylpropyl) imidazolium chloride is replaced with 3-methyl-1- (3-triethoxysilylmethyl) imidazolium chloride. was made. The composite semipermeable membrane thus obtained was evaluated in the same manner as in Example 1, and the performance shown in Table 1 was obtained.
- Coating solution A was prepared by adding 1.9 parts by weight of sodium p-styrenesulfonate, 2.6 parts by weight of 1-methyl-3- (3-trimethoxysilylpropyl) imidazolium chloride and 2,2-dimethoxy-1,2-diphenyl.
- coating solution B consisting of 0.15 parts by weight of ethane-1-one and 94.76 parts by weight of 65% isopropyl alcohol aqueous solution
- an excimer lamp UER20-172 manufactured by Ushio Electric Co., Ltd. capable of irradiating 172 nm ultraviolet rays was used.
- the composite semipermeable membrane obtained in Comparative Example 1 had low removal performance for both monovalent ions and divalent ions.
- the composite semipermeable membrane obtained by Example 1 and Example 2 has a large difference between the removal rate of monovalent ions and the removal rate of divalent ions, and is a composite semipermeable membrane having high selective separation. It has been shown.
- Comparative Example 2 A composite semipermeable membrane was prepared in the same manner as in Example 1 except that 3-methyl-1- (3-trimethoxysilylpropyl) imidazolium chloride was replaced with 3-aminopropyltrimethoxysilane. The composite semipermeable membrane thus obtained was evaluated in the same manner as in Example 1, and the performance shown in Table 1 was obtained.
- Comparative Example 3 On a microporous support membrane prepared by the same method as in Example 1, 0.8% by weight of piperazine, 0.2% by weight of 1,3-bis (4-piperidyl) propane, a surfactant (Japanese emulsifier ( New Coal 271A) 0.5% by weight and an aqueous solution containing 1.0% by weight of trisodium phosphate were applied, drained with an air knife, and then air-dried with warm air at 120 ° C. for 40 seconds. Thereafter, a 0.3 wt% decane solution of trimesic acid chloride was applied, and then heat treated with hot air at 100 ° C.
- a surfactant Japanese emulsifier ( New Coal 271A) 0.5% by weight
- an aqueous solution containing 1.0% by weight of trisodium phosphate were applied, drained with an air knife, and then air-dried with warm air at 120 ° C. for 40 seconds. Thereafter, a 0.3 wt%
- the composite semipermeable membrane obtained in Comparative Example 3 is more selective for divalent ions than monovalent ions compared to the composite semipermeable membranes obtained in Example 1 and Example 2. Inferior permeability was shown.
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- Life Sciences & Earth Sciences (AREA)
- Inorganic Chemistry (AREA)
- Environmental & Geological Engineering (AREA)
- Wood Science & Technology (AREA)
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- Water Supply & Treatment (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Separation Using Semi-Permeable Membranes (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
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Abstract
Description
(I)微多孔性支持膜上に分離機能層を有する複合半透膜であって、該分離機能層が、一般式(1)で表されるイオン群のうちから選ばれる少なくとも1種が縮合してなる縮合生成物、および、酸性基を少なくとも1種有する高分子の共役塩基からなることを特徴とする複合半透膜。
(II)酸性基がカルボキシル基、スルホン酸基、およびホスホン酸基のうちから選ばれる、少なくとも1種であることを特徴とする、(I)に記載の複合半透膜。
(III)高分子の共役塩基が少なくとも1つの重合可能な二重結合を有する化合物の共役塩基を少なくとも1種含む単量体または単量体混合物を重合してなることを特徴とする、(I)または(II)に記載の複合半透膜。
(IV)一般式(2)で表される化合物と、酸性基および少なくとも1つの重合可能な二重結合を有する化合物を少なくとも1種含む単量体または単量体混合物とを含む塗液を、微多孔性支持膜上に塗布し、エネルギー線を照射し、次に加熱乾燥させることにより、分離機能層を形成する工程を含むことを特徴とする複合半透膜の製造方法。
Flux(m3・m-2・日-1 )=(一日の透過液量)/(膜面積) ・・・式(4)
実施例1
21cm×15cmのポリエステル不織布(通気度0.5~1cc/cm2/sec)上にポリスルホンの15.3重量%ジメチルホルムアミド(DMF)溶液を200μmの厚みで室温(25℃)でキャストし、ただちに純水中に浸漬して5分間放置することによって微多孔性支持膜を作製した。
3-メチル-1-(3-トリメトキシシリルプロピル)イミダゾリウムクロリドを3-エチル-1-(3-トリメトキシシリルプロピル)イミダゾリウムクロリドに代える以外は実施例1と同様にして複合半透膜を作製した。また、このようにして得られた複合半透膜を実施例1と同様にして評価を行い、表1に示す性能が得られた。
3-メチル-1-(3-トリメトキシシリルプロピル)イミダゾリウムクロリドを3-ブチル-1-(3-トリメトキシシリルプロピル)イミダゾリウムクロリドに代える以外は実施例1と同様にして複合半透膜を作製した。また、このようにして得られた複合半透膜を実施例1と同様にして評価を行い、表1に示す性能が得られた。
3-メチル-1-(3-トリメトキシシリルプロピル)イミダゾリウムクロリドを3-メチル-1-(3-トリエトキシシリルメチル)イミダゾリウムクロリドに代える以外は実施例1と同様にして複合半透膜を作製した。また、このようにして得られた複合半透膜を実施例1と同様にして評価を行い、表1に示す性能が得られた。
塗液Aをp-スチレンスルホン酸ナトリウム1.9重量部、1-メチル-3-(3-トリメトキシシリルプロピル)イミダゾリウムクロリド2.6重量部、2,2-ジメトキシ-1,2-ジフェニルエタン-1-オン0.15重量部、65%イソプロピルアルコール水溶液94.76重量部からなる塗液Bに代え、172nmの紫外線が照射できるウシオ電機社製エキシマランプUER20-172を用い、照射窓と微多孔性支持膜の距離を1cmに設定し紫外線を10分間照射する工程を365nmの紫外線が照射できるハリソン東芝ライティング社製UV照射装置TOSCURE752を用い、照射強度を20mW/cm2に設定し、紫外線を20分間照射する工程に代える以外は実施例1と同様にして複合半透膜を作製した。また、このようにして得られた複合半透膜を実施例1と同様にして評価を行い、表1に示す性能が得られた。
3-メチル-1-(3-トリメトキシシリルプロピル)イミダゾリウムクロリドを3-クロロプロピルトリメトキシシランに代える以外は実施例1と同様にして複合半透膜を作製した。また、このようにして得られた複合半透膜を実施例1と同様にして評価を行い、表1に示す性能が得られた。
3-メチル-1-(3-トリメトキシシリルプロピル)イミダゾリウムクロリドを3-アミノプロピルトリメトキシシランに代える以外は実施例1と同様にして複合半透膜を作製した。また、このようにして得られた複合半透膜を実施例1と同様にして評価を行い、表1に示す性能が得られた。
実施例1と同様の方法にて作製した微多孔性支持膜上に、ピペラジン0.8重量%、1,3-ビス(4-ピペリジル)プロパン0.2重量%、界面活性剤(日本乳化剤(株)製、ニューコール271A)0.5重量%、リン酸三ナトリウム1.0重量%を含有した水溶液を塗布し、エアーナイフで液切りした後、120℃の温風で40秒間風乾した。その後、トリメシン酸クロライドの0.3重量%デカン溶液を塗布し、その後、100℃の熱風で5分間熱処理し、反応を進行させてから、炭酸ナトリウム5.0重量%とドデシル硫酸ナトリウム0.1重量%からなるアルカリ水溶液を塗布して反応を停止させ、複合半透膜を得た。また、このようにして得られた複合半透膜を実施例1と同様にして評価を行い、表1に示す性能が得られた。
Claims (4)
- 酸性基がカルボキシル基、スルホン酸基、およびホスホン酸基のうちから選ばれる、少なくとも1種であることを特徴とする、請求項1に記載の複合半透膜。
- 高分子の共役塩基が少なくとも1つの重合可能な二重結合を有する化合物の共役塩基を少なくとも1種含む単量体または単量体混合物を重合してなることを特徴とする、請求項1または2に記載の複合半透膜。
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JP2016013555A (ja) * | 2015-10-19 | 2016-01-28 | 株式会社東芝 | 脱塩処理膜、脱塩処理方法および脱塩処理装置 |
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WO2014022377A1 (en) * | 2012-07-30 | 2014-02-06 | Dow Corning Corporation | Membranes and coatings made from mixtures including ionic liquids having silicon-bonded hydrolyzable groups |
MA36586B1 (fr) * | 2013-12-18 | 2016-06-30 | Univ Hassan Ii Casablanca | Greffage des liquides ioniques sur des materiaux textiles par voie sol/gel pour le developpement de tissus a taches dediees |
WO2017150585A1 (ja) * | 2016-02-29 | 2017-09-08 | 東レ株式会社 | 積層半透膜 |
CN110505906A (zh) * | 2017-01-10 | 2019-11-26 | 得克萨斯州A&M大学系统 | 甲磺酸介导的共轭多孔聚合物网络的无溶剂合成 |
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EP2415515A1 (en) | 2012-02-08 |
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SG174896A1 (en) | 2011-11-28 |
JPWO2010113656A1 (ja) | 2012-10-11 |
CN102378645B (zh) | 2014-06-04 |
JP5459205B2 (ja) | 2014-04-02 |
US20120024778A1 (en) | 2012-02-02 |
AU2010231859A1 (en) | 2011-10-13 |
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US8739977B2 (en) | 2014-06-03 |
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