WO2012050156A1 - 抗アレルゲン剤 - Google Patents
抗アレルゲン剤 Download PDFInfo
- Publication number
- WO2012050156A1 WO2012050156A1 PCT/JP2011/073508 JP2011073508W WO2012050156A1 WO 2012050156 A1 WO2012050156 A1 WO 2012050156A1 JP 2011073508 W JP2011073508 W JP 2011073508W WO 2012050156 A1 WO2012050156 A1 WO 2012050156A1
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- Prior art keywords
- allergen
- acid
- resin
- agent
- pka
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- VZWXIQHBIQLMPN-UHFFFAOYSA-N chromane Chemical compound C1=CC=C2CCCOC2=C1 VZWXIQHBIQLMPN-UHFFFAOYSA-N 0.000 description 1
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- FPAFDBFIGPHWGO-UHFFFAOYSA-N dioxosilane;oxomagnesium;hydrate Chemical compound O.[Mg]=O.[Mg]=O.[Mg]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O FPAFDBFIGPHWGO-UHFFFAOYSA-N 0.000 description 1
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- 229910052731 fluorine Inorganic materials 0.000 description 1
- 229940074391 gallic acid Drugs 0.000 description 1
- 235000004515 gallic acid Nutrition 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 239000010438 granite Substances 0.000 description 1
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- 238000001746 injection moulding Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
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- 239000004579 marble Substances 0.000 description 1
- 239000006224 matting agent Substances 0.000 description 1
- 230000001404 mediated effect Effects 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 239000012454 non-polar solvent Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 235000014593 oils and fats Nutrition 0.000 description 1
- CMOAHYOGLLEOGO-UHFFFAOYSA-N oxozirconium;dihydrochloride Chemical compound Cl.Cl.[Zr]=O CMOAHYOGLLEOGO-UHFFFAOYSA-N 0.000 description 1
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- 239000005011 phenolic resin Substances 0.000 description 1
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- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920003225 polyurethane elastomer Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
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- 239000002964 rayon Substances 0.000 description 1
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- 235000005713 safflower oil Nutrition 0.000 description 1
- 239000003813 safflower oil Substances 0.000 description 1
- 238000007665 sagging Methods 0.000 description 1
- 230000008313 sensitization Effects 0.000 description 1
- 239000004208 shellac Substances 0.000 description 1
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
- 229940113147 shellac Drugs 0.000 description 1
- 235000013874 shellac Nutrition 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
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- 239000004945 silicone rubber Substances 0.000 description 1
- 230000036556 skin irritation Effects 0.000 description 1
- 231100000475 skin irritation Toxicity 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 150000003431 steroids Chemical class 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 229910052572 stoneware Inorganic materials 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 229920001864 tannin Polymers 0.000 description 1
- 239000001648 tannin Substances 0.000 description 1
- 235000018553 tannin Nutrition 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 229910000349 titanium oxysulfate Inorganic materials 0.000 description 1
- JUWGUJSXVOBPHP-UHFFFAOYSA-B titanium(4+);tetraphosphate Chemical compound [Ti+4].[Ti+4].[Ti+4].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O JUWGUJSXVOBPHP-UHFFFAOYSA-B 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 238000004506 ultrasonic cleaning Methods 0.000 description 1
- 238000001132 ultrasonic dispersion Methods 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
- XJUNLJFOHNHSAR-UHFFFAOYSA-J zirconium(4+);dicarbonate Chemical compound [Zr+4].[O-]C([O-])=O.[O-]C([O-])=O XJUNLJFOHNHSAR-UHFFFAOYSA-J 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
-
- 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
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/61—Additives non-macromolecular inorganic
- C09D7/62—Additives non-macromolecular inorganic modified by treatment with other compounds
-
- 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
- C09D201/00—Coating compositions based on unspecified macromolecular compounds
-
- 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
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
-
- 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
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/14—Paints containing biocides, e.g. fungicides, insecticides or pesticides
-
- 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
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/16—Antifouling paints; Underwater paints
- C09D5/1606—Antifouling paints; Underwater paints characterised by the anti-fouling agent
- C09D5/1612—Non-macromolecular compounds
- C09D5/1618—Non-macromolecular compounds inorganic
-
- 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
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/66—Additives characterised by particle size
- C09D7/67—Particle size smaller than 100 nm
-
- 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
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/66—Additives characterised by particle size
- C09D7/69—Particle size larger than 1000 nm
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/32—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond
- D06M11/36—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond with oxides, hydroxides or mixed oxides; with salts derived from anions with an amphoteric element-oxygen bond
- D06M11/46—Oxides or hydroxides of elements of Groups 4 or 14 of the Periodic Table; Titanates; Zirconates; Stannates; Plumbates
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/68—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with phosphorus or compounds thereof, e.g. with chlorophosphonic acid or salts thereof
- D06M11/70—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with phosphorus or compounds thereof, e.g. with chlorophosphonic acid or salts thereof with oxides of phosphorus; with hypophosphorous, phosphorous or phosphoric acids or their salts
- D06M11/71—Salts of phosphoric acids
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/77—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with silicon or compounds thereof
- D06M11/79—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with silicon or compounds thereof with silicon dioxide, silicic acids or their salts
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/20—Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
- Y10T442/2525—Coating or impregnation functions biologically [e.g., insect repellent, antiseptic, insecticide, bactericide, etc.]
Definitions
- the present invention relates to an anti-allergen agent comprising an inorganic powder having a specific acid point concentration, an anti-allergen composition containing the anti-allergen agent, and a product.
- Anti-allergens are sprayed and painted on textile products such as clothing, bedding, and masks, interior products such as filters, curtains, carpets, and furniture used in air cleaners and air conditioners, and automotive interior materials.
- textile products such as clothing, bedding, and masks
- interior products such as filters, curtains, carpets, and furniture used in air cleaners and air conditioners, and automotive interior materials.
- acaricides are generally used to control mites in house dust. Even after death, the allergens are gradually released as the worms decompose, so killing the mites does not inactivate the allergens. Also, the mask is used to prevent inhalation of pollen such as cedar, but the pollen adhering to the mask does not lose allergen activity, so there is a risk of inhalation by scattering again. .
- allergens that cause allergic symptoms are removed from the living space before being aspirated into the human body or denatured. It is necessary to make them harmless.
- ⁇ As a method for removing allergens without using chemicals
- a method of reducing allergens by physically removing floor accumulated dust and airborne dust with a vacuum cleaner or air cleaner there is a method of reducing allergens by physically removing floor accumulated dust and airborne dust with a vacuum cleaner or air cleaner.
- a large amount of allergen sucked by the electric vacuum cleaner is only stored in the dust bag, and there is a risk that the allergen is scattered again when the dust bag is discarded.
- it is difficult to completely remove the fine particulate matter by removal with an air cleaner and there is a risk of re-entrainment.
- Patent Documents 1 and 2 disclose methods using tannic acid which are similar compounds of tannic acid.
- Patent Document 3 discloses polyphenols such as tea extract and gallic acid which are similar compounds of tannic acid. Is disclosed.
- organic allergen reducing agents such as tannic acid are chemically unstable, and when attached to fibers and textiles, they may be colored or discolored over time, or the environment may be caused by moisture, oil, solvent or washing. The problem is that it spills into the skin and soils clothes and causes skin irritation.
- Patent Document 1 discloses that tannic acid can be removed with distilled water, it is clear that tannic acid is lost if fibers treated with tannic acid are washed repeatedly. Therefore, it is problematic to use it as an anti-allergen for textiles and textile products that may be washed or touched directly, and it can be used for textile products that are exposed to human eyes due to problems such as color tone, heat resistance, and durability. There was a drawback that the target was limited. In order to improve such a defect, an antiallergen agent composed of an inorganic substance has been proposed. Patent Document 4 discloses that an allergen is adsorbed using an inorganic substance such as activated carbon.
- Patent Document 5 discloses that among inorganic substances, those having high solid acid strength are excellent in antiallergen activity. However, even if the substance exhibits the same solid acid strength, there may be a significant difference in allergen inactivation performance, and the higher the solid acid strength is, the higher the anti-allergen activity is not always. There wasn't. Furthermore, it has become clear that when a solid acid having a very high solid acid strength is used to perform fiber processing in an aqueous system, the metal part of the processing apparatus may corrode.
- JP-A 61-44821 Japanese Patent Publication No. 2-16731 JP-A-6-279273 JP 2002-167332 A WO2009 / 044648 International pamphlet
- the present invention is an anti-allergen agent composed of an inorganic substance having high anti-allergen performance, excellent heat resistance and processability, little coloration and not flowing out with water, preferably a coating composition It is an object of the present invention to provide an anti-allergen agent that hardly causes corrosion or discoloration of a mechanical device even when used as a product or a resin composition, and an anti-allergen composition and an anti-allergen product using the same.
- the present invention is an anti-allergen agent comprising an inorganic powder having a pKa of 4.8 or less and an acid point concentration of 0.001 mmol / g or more, an anti-allergen composition using the anti-allergen agent, and an anti-allergen product.
- the anti-allergen agent of the present invention not only exhibits a high anti-allergen activity compared to existing anti-allergen agents, but also is an inorganic substance, so it has excellent heat resistance and little coloration or discoloration, and will flow out with water. It is durable because there is no. Excellent antiallergenicity can be imparted to various products by a simple processing method.
- the acid point concentration used in the anti-allergen agent of the present invention is the number of acid points or acidic centers on the surface of the solid, and can usually be expressed as the number per unit weight or unit surface area of the solid or the number of moles.
- the acid strength of the acid point that is included in the quantity of the acid point concentration can be expressed by pKa.
- the acid strength indicates the strength of the property that the acid point on the solid surface gives a proton to the base, or the property of receiving an electron pair from the base, and the property that gives a proton to the base as the pKa of the acid point is smaller, or The strength of accepting electron pairs from the base is increased, and the ability to adsorb and inactivate allergen proteins is increased.
- the acid strength at the acid point is small, that is, when the pKa is large, the property of giving a proton to the base or the property of receiving an electron pair from the base is weakened.
- the ability of the acid sites to adsorb and inactivate allergen proteins decreases, so that it becomes difficult to sufficiently adsorb allergen proteins no matter how large the number of acid sites, that is, the acid site concentration.
- This balance is also related to the structure of the allergen protein and the compatibility between the basicity and the acid point.
- the pKa of the acid point of the inorganic substance having an acid point is 4.8.
- the effect of inactivation was shown for any allergen protein, and the quantity of acid sites, that is, the acid site concentration and the anti-allergen effect were correlated regardless of the type of allergen protein. That is, it has been found that if an acid point concentration of a solid acid having an acid point pKa of 4.8 or less is measured, it can be used as an index of the antiallergen performance of the substance.
- the number of acid points of an inorganic substance powder having an acid point pKa of 4.8 or less is defined as the “acid point concentration” in the present invention, The larger this value, the higher the anti-allergen performance, which is a preferable anti-allergen agent. Specifically, those having an acid point concentration of 0.001 mmol / g or more are preferable. Although there is no upper limit that should not exceed the acid point concentration, since a powder of an inorganic substance exceeding 10 mmol / g is not generally known as a specific material, the usual upper limit is 10 mmol / g or less.
- Measurement of the number of acid points with a pKa of 4.8 or less is obtained by applying a titration method using an indicator corresponding to a pKa of 4.8 to measure the total of all acid points with a pKa of 4.8 or less.
- the value is defined as the acid point concentration having a pKa of 4.8 or less.
- the acid point concentration is more preferably 0.01 mmol / g or more, and more preferably the acid point concentration is 0.05 mmol / g or more.
- an inorganic substance having an acid point concentration of 0.05 mmol / g or more has an excellent anti-allergen effect and exhibits a high effect on various allergen substances.
- the acid point concentration can be determined by measuring the amount of base that reacts with the powder.
- the measurement in the liquid phase is a titration method
- the measurement in the gas phase is a gas chemical adsorption method
- the adsorption / desorption amount of He or hydrogen gas is a gas chemical adsorption method
- the reaction between the anti-allergen agent and the allergen in the present invention is a liquid-mediated reaction
- measurement by a titration method in a liquid phase is suitable.
- the method for measuring the acid point concentration of the inorganic powder by the titration method in the liquid phase is as follows.
- the inorganic powder dispersed in the nonpolar solvent is titrated with n-butylamine, and the end point of the titration is confirmed by the discoloration of the indicator.
- the indicator before the reaction exhibits a base type color, but when adsorbed on the inorganic powder, exhibits a conjugate acid type color.
- the acid point concentration is determined from the titration amount of n-butylamine required to return from the conjugate acid type color to the base type color.
- One solid acid point corresponds to one n-butylamine molecule.
- the titrating base must replace the indicator bound to the solid acid point, its basicity must be stronger than the basicity of the indicator.
- the indicator shows an acidic color due to solid acidity, but it is preferable to allow sufficient time until the reaction is completed.
- n-butylamine is dropped, and the acid point concentration is calculated from the amount of n-butylamine when the indicator color returns to the basic color.
- n-butylamine added in the system with the largest amount of n-butylamine in which no discoloration of the indicator is confirmed is defined as the amount of base reacted with the acid point and expressed as the acid point concentration (mmol / g).
- An inorganic substance having a high acid point concentration is an individual having many acid points on its surface.
- Specific examples of the inorganic substance having a high acid point concentration include, but are not limited to, amorphous magnesium silicate, ⁇ -type zirconium phosphate, layered titanium phosphate, activated alumina, activated titania, and the like. .
- the preferable average particle size is 0.01 to 50 ⁇ m, more preferably 0.02 to 20 ⁇ m.
- a powder having an average particle size of 0.01 ⁇ m or more has an advantage of being easy to handle because it is difficult to re-aggregate.
- particles having an average particle size of 50 ⁇ m or less have good dispersibility and do not impair the texture of the fiber. It is preferable because it has advantages such as being difficult to cause.
- the average value of the average particle diameter can be measured with a laser diffraction particle size distribution meter or the like, and the median diameter analyzed on a volume basis can be used as the representative value of the particle diameter.
- the color tone of the anti-allergen agent in the present invention is not limited, but white or a light color with high brightness is preferable in order to apply it to various materials and forms.
- the preferred brightness is 60 or more in terms of L value as measured by a color difference meter.
- the inorganic substance constituting the anti-allergen agent in the present invention preferably has an acid strength pKa of 1.5 or less. This is because, in addition to the high acid point concentration, the higher the acid strength as a solid acid, the higher the antiallergenicity.
- the acid strength of the anti-allergen agent in the present invention is the ability of the acid point on the surface of the anti-allergen agent to give a proton to the base or to receive an electron pair from the base.
- the acid strength can be measured by a method using an indicator. If an appropriate indicator is selected as the base, the acid strength can be measured as the ability to change the base type of the indicator to its conjugate acid type.
- the acid strength can be measured by using various acid-base conversion indicators with known acid strength (pKa). The more discolored indicator of pKa is, the higher its acid strength is.
- the method for measuring the acid strength of an inorganic solid acid using the indicator is as follows. Collect 0.1 g of solid acid in a test tube, add 2 mL of benzene and shake gently. Add 2 drops of 0.1% benzene solution of the indicator (however, crystal violet is not a benzene solution but a 0.1% ethanol solution) and shake gently to observe the color change.
- the acid strength of the solid acid is less than or equal to the strongest acid strength at which indicator discoloration was confirmed (ie, the lowest pKa value), and greater than the weakest acid strength at which indicator discoloration was not confirmed (ie, the highest pKa value).
- the pKa value of the inorganic solid acid is expressed as (the highest pKa value where no discoloration is confirmed) to (the lowest pKa value where discoloration is confirmed).
- the value is larger. Is generally written as.
- the inorganic substance in the present invention has a certain amount of water, so that an anti-allergen effect is easily exhibited.
- a preferable moisture content in the inorganic substance is preferably 0.5 wt% or more, more preferably 2 wt% or more, and further preferably 10 wt% or more.
- hygroscopic inorganic substances can be mixed with other materials or the moisture can be kept in the inorganic substance even if the atmospheric humidity changes, and the inorganic substance itself has the moisture necessary for allergen inactivation. Is excellent in terms of
- the anti-allergen effect in the present invention can be evaluated by an ELISA sandwich method widely used as an antigen detection and quantification method, and can be displayed as the allergen inactivation rate (unit%) shown in ⁇ Formula 1>. is there.
- the initial allergen amount is the allergen amount used in the ELISA evaluation and evaluated without using the sample, and the residual allergen amount is the allergen amount after contact with the sample.
- the usage form of the anti-allergen agent of the present invention is not particularly limited, and can be appropriately mixed with other components or combined with other materials depending on the application.
- it can be used in various forms such as powder, powder-containing dispersion, powder-containing particles, powder-containing paint, powder-containing fiber, powder-containing paper, powder-containing plastic, powder-containing film, and powder-containing aerosol.
- it can be used in combination with various additives or materials such as deodorants, antibacterial agents, antifungal agents, flameproofing agents, anticorrosives, fertilizers and building materials.
- allergens in living space can be prevented by adding to materials that may come into contact with humans, such as resin, paper, plastic, rubber, glass, metal, concrete, wood, paint, fiber, leather, and stone. It is possible to activate.
- the anti-allergen agent of the present invention as a coating composition containing a fixing agent (binder).
- a fixing agent binder
- an additive may be added to the coating composition, and the coating composition may be diluted with a solvent or water before being processed into products of various shapes.
- the larger the weight ratio of the anti-allergen agent / binder solid content the more easily the effect is produced.
- the larger the weight ratio of the binder solid content the more firmly fixed the anti-allergen agent and There are also favorable aspects.
- the weight ratio of the antiallergen agent / binder solids in the coating composition containing the antiallergen is preferably 90/10 to 30/70, more preferably 80/20 to 50/50.
- the concentration of the anti-allergen agent contained in the composition is preferably 0.5 to 50% by mass, more preferably 1 in terms of easy dispersion and good storage stability. ⁇ 30% by mass.
- the anti-allergen effect is manifested by the contact of the anti-allergen agent and the allergen on the surface of the product of various shapes, so fixing the anti-allergen agent on the surface of the product by the coating composition Since a large effect can be obtained with a smaller amount of the anti-allergen than when used for the entire interior of the product, it is preferable.
- binder used in the coating composition of the present invention examples include the following. Natural resin, natural resin derivative, phenol resin, xylene resin, urea resin, melamine resin, ketone resin, coumarone / indene resin, petroleum resin, terpene resin, cyclized rubber, chlorinated rubber, alkyd resin, polyamide resin, Polyvinyl chloride, acrylic resin, vinyl chloride / vinyl acetate copolymer resin, polyvinyl acetate, polyvinyl alcohol, polyvinyl plastic, chlorinated polypropylene, styrene resin, epoxy resin, urethane and cellulose derivatives. .
- acrylic resins polyvinyl chloride, and vinyl chloride / vinyl acetate copolymer resins are preferable.
- emulsion type resins are preferable because of low pollution and easy handling.
- pigments such as zinc oxide and titanium oxide, dyes, antioxidants, light stabilizers, flame retardants, antistatic agents, foaming agents, impact resistance enhancers, glass fibers, metal soaps
- Lubricants such as lubricants, moisture-proofing agents and extenders, coupling agents, nucleating agents, fluidity improvers, deodorants, wood powder, antifungal agents, antifouling agents, rust preventives, metal powders, UV absorbers, UV shielding Examples thereof include agents.
- a method of processing fibers with the coating composition containing the anti-allergen agent of the present invention there is a method of applying, dipping, or spraying a fiber or a fiber product with the coating composition as it is or diluted.
- the fibers that can be processed for example, natural fibers such as cotton, silk and wool, synthetic fibers such as polyester, nylon and acrylonitrile, semi-synthetic fibers such as triacetate and diacetate, and viscose rayon. Recycled fibers and the like, and composite fibers using two or more of these fibers may be used.
- it can be used also for the nonwoven fabric using polyethylene, a polypropylene, etc.
- the method of processing the anti-allergen agent of the present invention into a fiber or a fiber product is not particularly limited, but includes an immersion treatment, a printing treatment, a spraying treatment, etc., and the fiber is processed by drying the fiber containing the composition. Complete.
- the drying method can be any of natural drying, hot air drying, vacuum drying, etc., but is preferably a method using heat, preferably 40 ° C. to 250 ° C., preferably 50 ° C. to 180 ° C. for 1 minute to 5 hours, preferably
- the anti-allergen agent can be fixed to the fiber by drying for 5 minutes to 3 hours.
- the effect can be exhibited when the amount of the anti-allergen agent of the present invention attached to the fiber or fiber product is 0.1 g or more per 1 m 2 of the fiber or fiber product. On the other hand, it is preferably 20 g / m 2 or less, more preferably 1 g to 10 g / m 2 so as not to impair the physical properties and texture of the fiber or fiber product.
- the coating composition containing the anti-allergen agent of the present invention is too low in pH, it may corrode the metal of the production machine or cause deterioration of the processing solution or decrease in stability. Since the solid acid may be neutralized and the antiallergen effect may be reduced, the pH is preferably 3 or more and 9 or less when the coating composition is capable of pH measurement such as an aqueous system.
- the factor that determines the pH of the coating composition is the same as the pH of the aqueous dispersion of the inorganic powder, and is greatly affected by the pKa of the solid acid.
- the acid point concentration and the solubility of the anti-allergen agent itself are also included.
- the coating composition containing the anti-allergen agent of the present invention is non-aqueous, used as a paint containing various paint components, or used as a resin composition containing an anti-allergen agent, the metal part that contacts in the same manner
- a resin having a pH within a certain range in the aqueous dispersion test is less likely to cause rust and discoloration.
- the anti-allergen agent may be dispersed in deionized water so as to be 5 wt%, and the pH after stirring for 5 minutes with a stirrer at 25 ° C.
- the pH at that time is preferably 3 or more and 9 or less.
- Coating compositions, paints, resins, and the like using such anti-allergen agents are preferable because they hardly cause metal corrosion or discoloration.
- the paint since the paint is a composition intended for coating, it is a kind of coating composition, but not only for the purpose of fixing functional components such as anti-allergen agents but also for the cured coating film itself of the composition.
- a coating composition that maintains a certain level of strength and exhibits weather resistance, article surface protection and aesthetics is particularly called a paint.
- the anti-allergen agent of the present invention can be used in a paint.
- Various additives may be added to the paint.
- the resin component of the paint includes oils and fats such as soybean oil, linseed oil, safflower oil and castor oil, natural resins such as rosin, copar and shellac, processed resins such as chroman resin and petroleum resin, alkyd resins and acrylic resins. , Epoxy resin, polyurethane resin, vinyl chloride resin, silicone resin, synthetic resin such as fluororesin, rubber derivatives such as chlorinated rubber and cyclized rubber, cellulose such as nitrified cotton (lacquer), acetyl cellulose, etc. Derivatives and the like.
- the paint pigments are (white) titanium, (black) carbon, (brown) bengara, (red) chrome vermilion, (blue) bitumen, (yellow) yellow lead, (red) iron oxide, etc. Content, extender pigments such as calcium carbonate, talc and barite powder, rust preventive pigments such as red lead, lead suboxide and cyamido lead, functional pigments such as aluminum powder and zinc sulfide (fluorescent pigment).
- paint additives include UV curing agents, plasticizers, dispersants, anti-settling agents, emulsifiers, thickeners, antifoaming agents, antifungal agents, antiseptics, anti-skinning agents, drying agents, and anti-sagging agents.
- Matting agents antistatic agents, conductive agents, flame retardants, graffiti preventing agents and the like.
- the solvent for the paint include water, alcohol, paint thinner, lacquer thinner, polyurethane resin thinner, and the like. A paint can be prepared by combining these.
- a brush coating method, a roller method, or a spraying method is applied to a substrate prepared in advance with a liquid as it is or diluted. And iron coating method. Further, the coated paint may be cured by UV irradiation.
- base materials such as polyethylene, polyvinyl chloride, polyvinylidene chloride, polyvinyl alcohol, polypropylene, polyester, polycarbonate, polystyrene, polyacrylonitrile, cellophane, etc. , Joint materials such as PVC, modified silicon and urethane, metal, ceramic siding, porcelain, stoneware, pottery, glazed tile, marble, granite, glass and so on.
- the anti-allergen agent / paint solid content weight ratio in the paint containing the anti-allergen agent of the present invention is preferably 10/90 to 50/50, more preferably 20/80 to 40/60.
- An anti-allergen resin composition can be easily obtained by blending the anti-allergen agent of the present invention with a resin.
- a resin There is no restriction
- Specific resins may be molding resins, fiber resins, and rubber-like resins. For example, polyethylene, polypropylene, vinyl chloride, ABS resin, AS resin, MBS resin, nylon resin, polyester, polychlorinated resin.
- additives can also be contained.
- additives include pigments such as zinc oxide and titanium oxide, dyes, antioxidants, light stabilizers, flame retardants, antistatic agents, foaming agents, impact strength enhancers, glass fibers, and metal soaps.
- any known method can be adopted as a method for producing a resin composition by blending the anti-allergen agent of the present invention into a resin.
- a resin composition by blending the anti-allergen agent of the present invention into a resin.
- (1) using an additive for facilitating adhesion between the anti-allergen powder and the resin or a dispersant for improving the dispersibility of the anti-allergen powder, a pellet resin or a powder resin (2) A method of directly mixing with a mixer, (2) A method of mixing as described above, forming into pellets with an extrusion molding machine, and then blending the molded product into a pellet resin, (3) Antiallergen After the agent is molded into a high-concentration pellet using wax, the pellet-shaped product is blended with the pellet-shaped resin.
- the anti-allergen agent is dispersed and mixed in a high-viscosity liquid such as polyol.
- all known molding techniques and mechanical devices can be used in accordance with the characteristics of various resins. Mixing and mixing while heating and pressurizing or depressurizing at an appropriate temperature or pressure. Alternatively, they can be easily prepared by a kneading method, and their specific operation may be carried out by a conventional method, such as a lump, sponge, film, sheet, thread or pipe, or a composite thereof. It can be molded into various forms. If the anti-allergen agent / resin solids weight ratio in the resin composition containing the anti-allergen agent of the present invention is 10/90 or more, an obvious effect is easily exhibited.
- the solid weight ratio of the anti-allergen agent / resin composition in the resin composition containing the anti-allergen agent of the present invention is preferably 10/90 to 50/50, more preferably 20/80 to 40/60.
- the anti-allergen agent of the present invention can be used in the form of the above composition, resin composition, and resin molded product, as it is or depending on the application where allergen reduction is required, or mixed with other components as appropriate. Or can be used in combination with other materials. For example, it can be used in any form such as powder, liquid dispersion, granular, aerosol, or liquid.
- the anti-allergen agent of the present invention is used in various fields where allergen reduction is required, that is, indoor products, bedding, filters, furniture, in-car products, textile products, residential building products, paper products, toys, leather products. It can be used as toiletries, cosmetics and other products. For example, carpets, curtains, wall paper, tatami mats, shoji paper, wax for floors, calendars and other indoor products, bedding such as futons, beds, sheets, pillows, pillow covers, air purifiers, air conditioners Filters such as sofas, furniture such as chairs, car seats such as child seats and seat sheets, dust collection bags for vacuum cleaners, clothing, masks, stuffed animals, kitchen utensils, etc. However, the present invention is not limited to this.
- the average particle diameter of the inorganic powder described in the examples indicates a volume-based median diameter obtained by ultrasonic dispersion in deionized water using a laser diffraction particle size distribution analyzer. Unless otherwise specified,% indicates mass%, but the unit% of the allergen inactivation rate is according to the above ⁇ Formula 1>.
- To measure the acid point concentration put 0.5 g of inorganic powder in a 20 mL sample bottle, add 10 mL of benzene to it, and shake gently. Add 0.1N n-butylamine, which was added in 20 steps, and stir on a shaker.
- n-butylamine added in the largest amount of n-butylamine, in which no discoloration of methyl red was confirmed was defined as the amount of base reacted with acid sites, and the acid point concentration (mmol / g).
- the acid strength is less than or equal to the strongest acid strength (lowest pKa value) at which discoloration of the indicator was confirmed, and is considered to be greater than the weakest acid strength (highest pKa) at which the indicator did not discolor, so the range is defined as the pKa value. As recorded.
- the moisture content of the inorganic powder was weighed about 5 g in an aluminum cup that had been weighed at 250 ° C. for 1 hour in a dryer (weighed to the nearest 0.1 mg), dried for 2 hours at 250 ° C. in the dryer, and then weighed again. (Weighed to the nearest 0.1 mg), and the water content of the inorganic powder was expressed as a percentage by dividing the drying loss by the mass before drying.
- the anti-allergen effect was evaluated by the sandwich method of ELISA using a leopard mite allergen (allergen generally referred to as Derf2) and a cedar pollen allergen (allergen generally referred to as Cryj1).
- Derf2 a leopard mite allergen
- Cryj1 cedar pollen allergen
- An antibody coat well was prepared by a conventional method using a persimmon leopard mite allergen (Derf2) -specific antibody (15E11 antibody, manufactured by Asahivir Co., Ltd.). 3 mg of the sample was weighed, and 500 ⁇ L of leopard mite allergen (Derf2) prepared to 40 ng / mL with an antigen diluent was added.
- the mixture was well stirred to bring the sample into contact with the allergen, and then centrifuged and collected. The supernatant was collected, added to the 15E11 antibody coat well treated with a blocking agent, and allowed to stand at room temperature. One hour later, the sample was discarded, each well was washed with a washing buffer, and horseradish peroxidase-labeled anti-Derf2 monoclonal antibody 13A4PO (Asahivir Co., Ltd.) diluted to 200 ng / mL with the washing buffer was added to each well. It was added to the well and allowed to stand at room temperature.
- the test procedure by ELISA sandwich method using cedar pollen allergen is as follows.
- An antibody coat well was prepared by a conventional method using a cedar pollen allergen (Cryj1) specific antibody (Anti-Cryj1mAb013 manufactured by Seikagaku Corporation). 3 mg of the sample was weighed, and 500 ⁇ L of cedar pollen allergen (Cryj1) prepared to 10 ng / mL with the antigen dilution solution was added. The mixture was well agitated to bring the sample into contact with the allergen, and then centrifuged to collect the supernatant. The supernatant was added to the anti-Cryj1 mAb013 antibody coat well treated with a blocking agent and allowed to stand at room temperature.
- the pH of the aqueous dispersion of inorganic powder was dispersed in ion-exchanged water in a beaker so that the inorganic powder was 5 wt%, and the pH after stirring for 5 minutes with a stirrer at 25 ° C. was measured using a glass electrode pH meter. It measured using-.
- An iron test piece and an inorganic powder 5 wt% aqueous dispersion were placed in a glass test tube having a diameter of 30 mm, and placed on a heat block adjusted to 60 ° C. After 24 hours, the test piece was taken out, immersed in distilled water, subjected to ultrasonic cleaning for 5 minutes, and then dried for 30 minutes with a 50 ° C. dryer, and the presence or absence of rust on the test piece was visually confirmed.
- the anti-allergen effect of the processed fiber product is that cedar pollen allergen (Cryj1) is used as the allergen, and 25 cm 2 of fiber is put into a plastic bag with a chuck, and 1 mL of the allergen solution adjusted to 100 ng / mL is brought into contact with the sample for 1 hour. After that, the contact solution is spun down, the supernatant is collected, the absorbance is measured by the same ELISA method evaluation as that of the inorganic powder, and the anti-allergen inactivity according to the above formula 1 is compared with the absorbance when the sample is not used. % Conversion was evaluated.
- Anti-allergen effect film kneading resins allergens using cedar pollen allergen (Cryj1) to put the film 25 cm 2 into a zippered plastic bag, 1 hour contacting the allergen solution 1mL adjusted to the sample and 10 ng / mL Then, the contact liquid is centrifuged and the supernatant liquid is collected, and the absorbance is measured by the same ELISA method evaluation as that of the inorganic powder. Compared with the absorbance when the sample is not used, anti-allergen resistance is determined by the above formula 1. The activation rate% was evaluated.
- the anti-allergen effect of the film processed with the acrylic UV curable paint is the allergen solution using cedar pollen allergen (Cryj1) as the allergen, putting the film 25cm 2 into a plastic bag with a chuck, and adjusting the sample to 10ng / mL. After contacting 1 mL for 3 hours, the contact solution is spun down, the supernatant is collected, the absorbance is measured by the same ELISA method as for inorganic powder, and the above formula is compared with the absorbance when no sample is used.
- the anti-allergen inactivation rate% was evaluated according to 1.
- Table 1 shows the average particle size, water content, acid strength, and the mite allergen inactivation effect and the cedar pollen allergen inactivation effect measured by the ELISA method for the obtained amorphous magnesium silicate.
- Table 2 shows the results of measurement of color tone, pH of 5 wt% aqueous dispersion, colorability of PP plate, and metal corrosivity.
- Example 2 ⁇ -type zirconium phosphate
- a 15% zirconium oxychloride aqueous solution was added to a 75% phosphoric acid aqueous solution and aged at 120 ° C. for 12 hours, and then the precipitate was filtered, washed with water, dried and crushed to obtain ⁇ -type.
- a zirconium phosphate powder was obtained.
- Table 1 shows the average particle size, water content, acid strength, and mite allergen inactivation effect and cedar pollen allergen inactivation effect measured by the ELISA method of the obtained ⁇ -type zirconium phosphate.
- Table 2 shows the results of measurement of color tone, pH of 5 wt% aqueous dispersion, colorability of PP plate, and metal corrosivity.
- Example 3 A precipitate obtained by using titanyl sulfate and oxalic acid as an active titanium oxide raw material was filtered, dried, calcined at 500 ° C, and pulverized to prepare active titanium oxide.
- the average particle diameter, water content, acid strength and the mite allergen inactivating effect and the cedar pollen allergen inactivating effect measured by the ELISA method of the obtained titanium oxide are shown in Table 1.
- Table 2 shows the results of measurement of color tone, pH of 5 wt% aqueous dispersion, colorability of PP plate, and metal corrosivity.
- Example 4 The average particle diameter, acid strength, and mite allergen inactivation effect and cedar pollen allergen inactivation effect of activated white clay (Galeon Ace SH manufactured by Mizusawa Chemical Industry) were measured. The results are shown in Table 1. Table 2 shows the results of measurement of color tone, pH of 5 wt% aqueous dispersion, colorability of PP plate, and metal corrosivity.
- Table 1 shows the average particle diameter, water content, acid strength, and the mite allergen inactivating effect and the cedar pollen allergen inactivating effect measured by the ELISA method of the obtained crystalline magnesium silicate.
- Table 2 shows the results of measurement of color tone, pH of 5 wt% aqueous dispersion, colorability of PP plate, and metal corrosivity.
- a zirconium carbonate aqueous solution was added to a 75% phosphoric acid aqueous solution, heated and refluxed at 98 ° C. for 24 hours, and then the precipitate was filtered, washed with water, dried and crushed to obtain ⁇ -type phosphoric acid.
- Zirconium was obtained.
- Table 1 shows the average particle diameter, water content, acid strength, and mite allergen inactivation effect and cedar pollen allergen inactivation effect measured by ELISA method for the obtained ⁇ -type zirconium phosphate.
- Table 2 shows the results of measurement of color tone, pH of 5 wt% aqueous dispersion, colorability of PP plate, and metal corrosivity.
- Titanium oxide Commercially available titanium oxide (MC-50 manufactured by Ishihara Sangyo Co., Ltd.) The average particle diameter, acid strength, and the results of measuring the mite allergen inactivation effect and the cedar pollen allergen inactivation effect by ELISA method It is shown in Table 1.
- Table 2 shows the results of measurement of color tone, pH of 5 wt% aqueous dispersion, colorability of PP plate, and metal corrosivity.
- Activated Alumina Results of measuring the mean particle diameter, acid strength, and mite allergen inactivation effect and cedar pollen allergen inactivation effect of commercially available activated alumina (Mizusawa Chemical Industry GNDY-2) by ELISA method Is shown in Table 1.
- Table 2 shows the results of measurement of color tone, pH of 5 wt% aqueous dispersion, colorability of PP plate, and metal corrosivity.
- Example 9 Anti-allergen activity evaluation in the case where Example 1 is not fixed to the fiber
- a comparative fabric was prepared by the same processing method as Example 7 without using amorphous magnesium silicate which is an inorganic substance of Example 1. did.
- Table 3 shows the results of measuring the cedar pollen allergen inactivating effect of the comparative cloth.
- Example 9 Evaluation of heat resistance of Example 1 fixed to fiber After producing anti-allergen cloth in the same manner as in Example 7 and applying heat at 120 ° C. for 100 hours, the anti-allergen cloth was inactivated by cedar pollen allergen and discolored. The results of measuring the properties are shown in Table 4.
- Example 10 Evaluation of heat resistance of Example 1 fixed to fiber After producing anti-allergen cloth by the same method as in Example 8 and applying heat at 120 ° C. for 100 hours, the inactivation effect and discoloration of cedar pollen allergen of anti-allergen cloth The results of measuring the properties are shown in Table 4.
- the anti-allergen-processed cloth applied with amorphous magnesium silicate of Example 1 shows a sufficiently high allergen inactivation rate even when heat is applied for a long time, and no discoloration occurs.
- the anti-allergen product obtained by post-processing the inorganic substance of the present invention into a fiber has excellent heat resistance.
- Example 11 Water resistance evaluation of Example 1 fixed to fiber An anti-allergen cloth was prepared in the same manner as in Example 7, put into a plastic container, added with ion-exchanged water, and shaken at 25 ° C for 16 hours. Table 5 shows the results of measuring the cedar pollen allergen inactivating effect of the anti-allergen cloth dried at 120 ° C. for 30 minutes.
- Example 12 Water resistance evaluation of Example 1 fixed to fiber An anti-allergen cloth was prepared in the same manner as in Example 8, put into a plastic container, added with ion-exchanged water, and shaken at 25 ° C for 16 hours. Table 5 shows the results of measuring the cedar pollen allergen inactivating effect of the anti-allergen cloth dried at 120 ° C. for 30 minutes.
- the anti-allergen-processed cloth impregnated with amorphous magnesium silicate of Example 1 showed a sufficiently high allergen inactivation rate even after water treatment. Therefore, the anti-allergen product obtained by post-processing the inorganic substance of the present invention into a fiber has excellent water resistance.
- Example 13 Anti-allergen activity evaluation of Example 1 kneaded into resin Amorphous magnesium silicate, which is an inorganic substance of Example 1, and powdered polypropylene are mixed so as to have a mass ratio of 10:90 at 220 ° C. Was heated and pressed to produce an antiallergen film having a thickness of 0.2 mm. Table 6 shows the results of measuring the cedar pollen allergen inactivating effect of the anti-allergen film.
- Example 14 Anti-allergen activity evaluation of Example 1 kneaded into resin Amorphous magnesium silicate, which is an inorganic substance of Example 1, and powdered polypropylene were mixed at a solid content mass ratio of 20:80, and 220 ° C. Was heated and pressed to produce an antiallergen film having a thickness of 0.2 mm.
- Table 6 shows the results of measuring the cedar pollen allergen inactivating effect of the anti-allergen film.
- Example 10 Anti-allergen activity evaluation when Example 1 was not kneaded into the resin
- a comparative film was prepared by the same processing method as Example 13 without using amorphous magnesium silicate which is an inorganic substance of Example 1.
- Table 6 shows the results of measuring the cedar pollen allergen inactivating effect of the comparative film.
- the anti-allergen-processed film obtained by kneading the amorphous magnesium silicate of Example 1 showed a high allergen inactivation rate by adding 20 wt%. Therefore, the performance of the anti-allergen product obtained by kneading the inorganic substance of the present invention into a resin is excellent.
- Example 15 Evaluation of anti-allergen activity of Example 1 processed with UV curable resin Amorphous magnesium silicate, which is an inorganic substance of Example 1, and acrylic UV curable paint (no solvent) have a solid content mass ratio of 15:85 And then processed to a PET film (Toray Lumira T60-50) to a thickness of 15 ⁇ m using a bar coater, and a conveyor pressure using a high-pressure mercury lamp (strength 60 W / cm) at a distance of 25 cm. The composition was cured by irradiating with ultraviolet rays under a condition of 3.7 m / min to produce an anti-allergen film. Table 7 shows the results of measuring the cedar pollen allergen inactivating effect of the anti-allergen film.
- Example 16 Anti-allergen activity evaluation of Example 1 processed with UV curable resin Amorphous magnesium silicate, which is an inorganic substance of Example 1, and acrylic UV curable paint are mixed so that the solid content mass ratio is 30:70.
- a PET film Toray Lumilar T60-50
- a high-pressure mercury lamp strength 60 W / cm
- Table 7 shows the results of measuring the cedar pollen allergen inactivating effect of the anti-allergen film.
- Example 11 Evaluation of anti-allergen activity of a film processed with an acrylic UV curable paint when Example 1 is not fixed. Comparison is made by the same processing method as Example 15 without using amorphous magnesium silicate which is an inorganic substance of Example 1. A film was prepared. Table 7 shows the results of measuring the cedar pollen allergen inactivating effect of the comparative film.
- the anti-allergen film obtained by UV-curing the amorphous magnesium silicate of Example 1 showed a high anti-allergen inactivation rate. Therefore, the performance of the anti-allergen product in which the inorganic substance of the present invention is UV-cured on the surface is excellent.
- Example 17 In order to evaluate the antiallergenicity in an actual use environment, an amorphous magnesium silicate which is an inorganic substance was converted into an acrylic emulsion binder (NW-7060 manufactured by Toagosei Co., Ltd., solid content concentration 50 wt. %) And the mass ratio of the solid content of 2: 1 are immersed in a bath towel (155 cm ⁇ 70 cm component: cotton) for 5 minutes, and then dried at 120 ° C. for 60 minutes, An anti-allergen cloth (bath towel) having a fixed amount of 2 g / m 2 was prepared.
- NW-7060 manufactured by Toagosei Co., Ltd., solid content concentration 50 wt. %
- the cedar pollen floating in the environment was adsorbed on a sunny day with cedar pollen scattered by bathing a bath towel on the outdoor clothes for 6 hours.
- a vacuum cleaner with a nonwoven fabric set after standing overnight was applied to the entire surface of the bath towel, and the allergen was sucked and collected on the nonwoven fabric.
- the allergen placed on the nonwoven fabric was extracted with 10 ml of an antigen dilution solution (0.1% BSA + PBS buffer), and the amount of cedar pollen allergen (Cryj1) was measured by ELISA to obtain the allergen recovery amount.
- Table 8 shows the results of allergen recovery by conducting the same adsorption test three times on another sunny day with more than three days. It was. The meaning of the first, second and third days in Table 8 means that the adsorption test was performed three different days.
- Comparative Example 12 A bath towel of Comparative Example 12 was prepared in the same manner as in Example 17 except that only a binder containing no amorphous magnesium silicate was used, and it floated in the environment in the same place on the same day as Example 17. To adsorb cedar pollen. The results of the allergen recovery amount are shown in Table 8.
- the anti-allergen agent of the present invention it is possible to impart a function to inactivate allergens derived from pollen, mites, etc. to materials related to human living space such as textile products and housing building materials, Allergen products can be manufactured.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Wood Science & Technology (AREA)
- Inorganic Chemistry (AREA)
- Nanotechnology (AREA)
- Textile Engineering (AREA)
- Plant Pathology (AREA)
- Paints Or Removers (AREA)
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US13/879,264 US20130273798A1 (en) | 2010-10-14 | 2011-10-13 | Anti-allergen agent |
KR1020137011896A KR101893232B1 (ko) | 2010-10-14 | 2011-10-13 | 항알레르겐제 |
JP2012538710A JP5594367B2 (ja) | 2010-10-14 | 2011-10-13 | 抗アレルゲン剤 |
CN201180049385.5A CN103261357B (zh) | 2010-10-14 | 2011-10-13 | 抗变应原剂 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2010231123 | 2010-10-14 | ||
JP2010-231123 | 2010-10-14 |
Publications (1)
Publication Number | Publication Date |
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WO2012050156A1 true WO2012050156A1 (ja) | 2012-04-19 |
Family
ID=45938380
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/JP2011/073508 WO2012050156A1 (ja) | 2010-10-14 | 2011-10-13 | 抗アレルゲン剤 |
Country Status (5)
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US (1) | US20130273798A1 (zh) |
JP (1) | JP5594367B2 (zh) |
KR (1) | KR101893232B1 (zh) |
CN (1) | CN103261357B (zh) |
WO (1) | WO2012050156A1 (zh) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2017075420A (ja) * | 2015-10-14 | 2017-04-20 | 住化エンバイロメンタルサイエンス株式会社 | 繊維用アレルゲン低減化組成物 |
WO2017150063A1 (ja) * | 2016-03-01 | 2017-09-08 | 東亞合成株式会社 | 抗ウイルス剤、コーティング組成物、樹脂組成物及び抗ウイルス製品 |
WO2020105227A1 (ja) * | 2018-11-22 | 2020-05-28 | 日揮ユニバーサル株式会社 | エアフィルター用濾材及びエアフィルター用濾材の製造方法 |
JP2020164604A (ja) * | 2019-03-28 | 2020-10-08 | 住化エンバイロメンタルサイエンス株式会社 | アレルゲン低減化組成物 |
WO2021182299A1 (ja) * | 2020-03-13 | 2021-09-16 | 東亞合成株式会社 | リン酸ジルコニウム粒子、及びこれを使用した塩基性ガス消臭剤、並びにそれらの製造方法 |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3848108A1 (de) * | 2020-01-09 | 2021-07-14 | Carl Freudenberg KG | Filtermedium mit antiallergenen substanzen |
CN113388459B (zh) | 2021-05-26 | 2022-03-01 | 宁波芮颂生物科技有限公司 | 一种抗猫、狗过敏原整理组合物溶液的制备方法 |
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WO2009044648A1 (ja) * | 2007-10-01 | 2009-04-09 | Toagosei Co., Ltd. | 抗アレルゲン剤 |
JP2010235701A (ja) * | 2009-03-30 | 2010-10-21 | Toagosei Co Ltd | 抗アレルゲン性組成物および抗アレルゲン性製品 |
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US3940498A (en) * | 1974-09-03 | 1976-02-24 | Johns-Manville Corporation | Chill-proofing with synthetic magnesium silicates |
DE3575860D1 (de) | 1984-07-11 | 1990-03-15 | Univ Sydney | Antiallergikum. |
IT1191613B (it) * | 1985-05-15 | 1988-03-23 | Eniricerche Spa | Fosfato di zirconio e suo metodo di preparazione |
JPH0216731A (ja) | 1988-07-05 | 1990-01-19 | Mitsubishi Electric Corp | プラズマ反応装置 |
JPH06279273A (ja) | 1993-03-30 | 1994-10-04 | Earth Chem Corp Ltd | 環境からアレルゲンを除去する方法および抗ア レルゲン組成物 |
JP2002167332A (ja) | 2000-11-30 | 2002-06-11 | Lion Corp | アレルゲン吸着組成物 |
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2011
- 2011-10-13 US US13/879,264 patent/US20130273798A1/en not_active Abandoned
- 2011-10-13 CN CN201180049385.5A patent/CN103261357B/zh not_active Expired - Fee Related
- 2011-10-13 JP JP2012538710A patent/JP5594367B2/ja active Active
- 2011-10-13 WO PCT/JP2011/073508 patent/WO2012050156A1/ja active Application Filing
- 2011-10-13 KR KR1020137011896A patent/KR101893232B1/ko active IP Right Grant
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JPS6368527A (ja) * | 1986-09-10 | 1988-03-28 | Kuraray Co Ltd | Hb抗原不活化剤 |
JP2006265498A (ja) * | 2005-03-25 | 2006-10-05 | Fumakilla Ltd | アレルゲン失活剤 |
WO2009044648A1 (ja) * | 2007-10-01 | 2009-04-09 | Toagosei Co., Ltd. | 抗アレルゲン剤 |
JP2010235701A (ja) * | 2009-03-30 | 2010-10-21 | Toagosei Co Ltd | 抗アレルゲン性組成物および抗アレルゲン性製品 |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2017075420A (ja) * | 2015-10-14 | 2017-04-20 | 住化エンバイロメンタルサイエンス株式会社 | 繊維用アレルゲン低減化組成物 |
WO2017150063A1 (ja) * | 2016-03-01 | 2017-09-08 | 東亞合成株式会社 | 抗ウイルス剤、コーティング組成物、樹脂組成物及び抗ウイルス製品 |
JPWO2017150063A1 (ja) * | 2016-03-01 | 2019-01-24 | 東亞合成株式会社 | 抗ウイルス剤、コーティング組成物、樹脂組成物及び抗ウイルス製品 |
WO2020105227A1 (ja) * | 2018-11-22 | 2020-05-28 | 日揮ユニバーサル株式会社 | エアフィルター用濾材及びエアフィルター用濾材の製造方法 |
JPWO2020105227A1 (ja) * | 2018-11-22 | 2021-10-07 | 日揮ユニバーサル株式会社 | エアフィルター用濾材及びエアフィルター用濾材の製造方法 |
JP7205046B2 (ja) | 2018-11-22 | 2023-01-17 | 日揮ユニバーサル株式会社 | エアフィルター用濾材及びエアフィルター用濾材の製造方法 |
JP2020164604A (ja) * | 2019-03-28 | 2020-10-08 | 住化エンバイロメンタルサイエンス株式会社 | アレルゲン低減化組成物 |
WO2021182299A1 (ja) * | 2020-03-13 | 2021-09-16 | 東亞合成株式会社 | リン酸ジルコニウム粒子、及びこれを使用した塩基性ガス消臭剤、並びにそれらの製造方法 |
Also Published As
Publication number | Publication date |
---|---|
JP5594367B2 (ja) | 2014-09-24 |
CN103261357B (zh) | 2014-12-31 |
KR101893232B1 (ko) | 2018-08-29 |
JPWO2012050156A1 (ja) | 2014-02-24 |
US20130273798A1 (en) | 2013-10-17 |
CN103261357A (zh) | 2013-08-21 |
KR20130118881A (ko) | 2013-10-30 |
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