Classifications

• • 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
  • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
  • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
  • D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
  • D06M15/263—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
  • D06M15/277—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof containing fluorine
• • A—HUMAN NECESSITIES
  • A41—WEARING APPAREL
  • A41D—OUTERWEAR; PROTECTIVE GARMENTS; ACCESSORIES
  • A41D31/00—Materials specially adapted for outerwear
• • D—TEXTILES; PAPER
  • D03—WEAVING
  • D03D—WOVEN FABRICS; METHODS OF WEAVING; LOOMS
  • D03D15/00—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used
• • D—TEXTILES; PAPER
  • D03—WEAVING
  • D03D—WOVEN FABRICS; METHODS OF WEAVING; LOOMS
  • D03D15/00—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used
  • D03D15/20—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the material of the fibres or filaments constituting the yarns or threads
  • D03D15/208—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the material of the fibres or filaments constituting the yarns or threads cellulose-based
  • D03D15/217—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the material of the fibres or filaments constituting the yarns or threads cellulose-based natural from plants, e.g. cotton
• • D—TEXTILES; PAPER
  • D03—WEAVING
  • D03D—WOVEN FABRICS; METHODS OF WEAVING; LOOMS
  • D03D15/00—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used
  • D03D15/20—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the material of the fibres or filaments constituting the yarns or threads
  • D03D15/283—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the material of the fibres or filaments constituting the yarns or threads synthetic polymer-based, e.g. polyamide or polyester fibres
• • D—TEXTILES; PAPER
  • D03—WEAVING
  • D03D—WOVEN FABRICS; METHODS OF WEAVING; LOOMS
  • D03D15/00—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used
  • D03D15/40—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the structure of the yarns or threads
  • D03D15/47—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the structure of the yarns or threads multicomponent, e.g. blended yarns or threads
• • 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
  • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
  • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
  • D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
  • D06M15/327—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated alcohols or esters thereof
  • D06M15/333—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated alcohols or esters thereof of vinyl acetate; Polyvinylalcohol
• • 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
  • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
  • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
  • D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
  • D06M15/39—Aldehyde resins; Ketone resins; Polyacetals
  • D06M15/423—Amino-aldehyde resins
• • 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
  • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
  • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
  • D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
  • D06M15/53—Polyethers
• • 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
  • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
  • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
  • D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
  • D06M15/564—Polyureas, polyurethanes or other polymers having ureide or urethane links; Precondensation products forming them
  • D06M15/576—Polyureas, polyurethanes or other polymers having ureide or urethane links; Precondensation products forming them containing fluorine
• • 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
  • D06M2101/00—Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
  • D06M2101/02—Natural fibres, other than mineral fibres
  • D06M2101/04—Vegetal fibres
  • D06M2101/06—Vegetal fibres cellulosic
• • 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
  • D06M2101/00—Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
  • D06M2101/16—Synthetic fibres, other than mineral fibres
  • D06M2101/30—Synthetic polymers consisting of macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
  • D06M2101/32—Polyesters
• • 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
  • D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
  • D06M2200/01—Stain or soil resistance
• • 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
  • D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
  • D06M2200/10—Repellency against liquids
  • D06M2200/11—Oleophobic properties
• • D—TEXTILES; PAPER
  • D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
  • D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
  • D10B2331/00—Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products
  • D10B2331/04—Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products polyesters, e.g. polyethylene terephthalate [PET]

Definitions

• the present invention relates to a fiber structure having high soil resistance.
• addition of a hydrophilic resin to the fiber structure has the problem that when aqueous soil adheres, the soil is apt to expand greatly. Further, addition of a water-repellent and oil-repellent resin to a fiber structure has the problem that affinity between a washing liquid and aqueous soil is reduced due to water repellency, so that once adhering, soil is hardly washed out, and the fiber structure is easily soiled again.
• Patent Documents 1 and 2 suggest a water-absorbing and oil-repellent soil resistance processing method in which a film of a fluorine-based water repellent having a hydrophilic component is formed.
• Patent Document 3 suggests a water-repellent and oil-repellent soil resistance processing method in which a fluorine-based water repellent to a fiber fabric using a non-blocking-type water-dispersed isocyanate crosslinking agent.
• Patent Document 4 suggests a water-repellent and oil-repellent soil resistance processing method in which a film of a mixture of a polymer composed of a triazine ring-containing polymerizable monomer and a fluorine-based water repellent having a hydrophilic component is formed on a surface of single fiber.
• Patent Document 5 suggests Patent Documents 1 and 2 suggest a low-water-repellent and oil-repellent soil resistance processing method in which a film of a fluorine-based water repellent having a hydrophilic component, whose mass concentration ratio of oxygen atoms to fluorine atoms is adjusted, is formed.
• Patent Documents 1 and 2 have the problem that because of high hydrophilicity, aqueous soil is apt to expand once the soil adheres.
• the processing method suggested in Patent Document 3 has the problem that since high water repellency is exhibited, affinity between a washing liquid and aqueous soil during washing tends to be reduced, leading to deterioration of soil removability in washing, and in particular, soil removability after processing is low.
• the processing method suggested in Patent Document 4 has the problem that since a large amount of a polymer composed of a triazine ring-containing polymerizable monomer, fluororesin and hydrophilic components are buried, so that sufficient soil resistant cannot be exhibited.
• Patent Document 5 ensures high washing durability, but has the problem that soil resistance after processing may be low.
• an object of the present invention is to provide a fiber structure having both adhesion suppressibility against aqueous soil and oily soil and soil removability even after being repeatedly washed after processing.
• the present invention employs the following means for solving the problems described above.
• the soil resistant fiber structure of the present invention includes on at least a part of a fiber surface a resin film containing polyvinyl alcohol and a fluorine-based oil-repellent resin having a hydrophilic component.
• a soil resistant fiber structure of the present invention includes a film on at least a part of a fiber surface, the film containing polyvinyl alcohol and a fluorine-based oil-repellent resin having a hydrophilic component, the fiber structure having a water repellency degree of 2 or less as measured by a spray test in accordance with JIS L-1092, and an oil repellency degree of 2 or more as measured in accordance with AATCC 118 method.
• the oil repellency degree is 2 or more, sufficient oil repellency is exhibited, so that soil hardly adheres to the fiber. Further, the oil repellency degree is preferably 5 or more. Since the water repellency degree is 2 or less, sufficient hydrophilicity is exhibited, and thus affinity can be maintained between the fiber and a washing liquid, so that the washing liquid can penetrate the inside of the fiber structure without being repelled during washing, and come into contact with soil to remove the soil.
• the present invention provides a low-water-repellent and oil-repellent fiber structure which has reduced water repellency and has oil repellency, and is thus capable of exhibiting high soil resistance. Further, washing durability can be improved by performing control so that the water repellency degree falls within a more appropriate range of low water repellency.
• the oil repellency of the fiber structure is a value determined in accordance with AATCC 118 method (2013), and the water repellency degree of the fiber structure is a value determined by a spray method in accordance with JIS L 1092, "Testing Methods for Water Resistance of Textiles” (2009) .
• a fluorine-based oil-repellent resin and polyvinyl alcohol are preferably used which ensure that the oil repellency degree is 2 or more and the water repellency degree is 2 or less when a film containing the fluorine-based oil-repellent resin and the polyvinyl alcohol is formed on a fiber surface.
• the fluorine-based oil-repellent resin having a hydrophilic component is preferably a fluorine-containing copolymer having a repeating unit derived from a vinyl monomer having a perfluoroalkyl group and a vinyl monomer having a hydrophilic functional group (hydrophilic vinyl monomer).
• hydrophilic vinyl monomer examples include vinyl monomers containing a hydrophilic functional group such as a sulfonyl group, a sulfonyl base, a carboxyl group, a carboxyl base, an ammonium group, an ammonium base, an oxyalkylene group or a polyoxyalkylene group.
• vinyl monomers represented by the following general formula (II) are preferable.
• R 1 is normally H or an alkyl group having 1 to 4 carbon atoms, preferably H or CH 3 .
• -(R 2 O) n represents an oxyalkylene group or a polyoxyalkylene group.
• R 2 is preferably an alkylene group having 2 to 5 carbon atoms, more preferably CH 2 CH 2 , CH 2 CH 2 CH 2 or CH 2 (CH 3 )CH 2 from the viewpoint of ensuring that hydrophilicity can be controlled to fall within a further preferred range.
• R 3 normally represents H or CH 3 .
• n is a polymerization degree, and represents 1 to 20.
• the fluorine-based oil-repellent resin that is preferably used in the present invention is preferably one having a water absorbability of 40 seconds or more as measured by a dropping method in accordance with JIS L 1907 (2010) a water repellency degree of 2 or less, and an oil repellency degree of 2 or more. Further, low water repellency corresponding to a water absorbability of 60 seconds or more is more preferable from the viewpoint of improving washing durability for soil removability against pressed soil. In addition, the oil repellency degree is more preferably 7 or less from the viewpoint of a balance between resistance to adhesion of soil and affinity with washing water.
• the ratio of the vinyl monomer having a perfluoroalkyl group and the hydrophilic vinyl monomer in the fluorine-containing copolymer which is preferably used is not limited as long as the ratio satisfies the range specified in the present invention, and it is preferable that by the following method, control is performed so as to obtain low water repellency and oil repellency and water-absorption and oil repellency.
• the control can be performed by the following method. That is, by increasing the ratio of the vinyl monomer containing a hydrophilic functional group, water repellency can be suppressed, and for enhancing oil repellency, the ratio of the vinyl monomer having a perfluoroalkyl group may be increased.
• the hydrophilicity of the vinyl monomer containing a hydrophilic functional group may be enhanced.
• the ratio of the hydrophilic functional group can be increased, or a functional group having higher hydrophilicity can be selected as the hydrophilic functional group.
• the hydrophilic functional group is preferably an oxyalkylene group (more preferably an oxyethylene group) or a polyoxyalkylene group (more preferably a polyoxyethylene group). When a polyoxyalkylene group is used, hydrophilicity can be enhanced as the polymerization degree thereof is increased.
• the fluorine-based oil-repellent resin having a hydrophilic component satisfying the above-described condition is preferably one that exhibits performance classified as that of a so-called water-absorbing and oil-repellent type with a water repellency degree of 2 or less (preferably 1), an oil repellency degree of 2 or more and a water absorbability of less than 40 seconds or a low-water-repellent and oil-repellent type with a water repellency degree of 2 or less, an oil repellency degree of 2 or more and a water absorbability of 40 seconds or more, particularly preferably one classified as a low-water-repellent and oil-repellent type, when the resin is added to the fiber structure.
• a so-called water-absorbing and oil-repellent type with a water repellency degree of 2 or less preferably 1
• Examples of the commercially available product include “PARAZINE” KFS-100 (manufactured by KEIHIN CHEMICAL CO., LTD.) which is classified as a low-water-repellent and oil-repellent type, and “PARAZINE” KFS-150 (manufactured by KEIHIN CHEMICAL CO., LTD.) which is classified as a water-absorbing and oil-repellent type.
• the fluorine-based oil-repellent resin has a perfluorooctanoic acid and perfluorooctanesulfonic acid content below a detection limit.
• the term "below a detection limit” means that the concentration of each of perfluorooctanoic acid and perfluorooctanesulfonic acid, precursors thereof and salts thereof measured with the following high-performance liquid chromatograph-mass spectrometer (LC-MS) is each less than 5 ng/g.
• Polyvinyl alcohol may be produced by saponifying polyvinyl acetate.
• the saponification degree of polyvinyl alcohol is, normally, preferably 70 to 99%, more preferably 80 to 95%.
• the average polymerization degree and the saponification degree are values obtained by performing measurement in accordance with JIS K 6726 (1994), paragraphs 3.7 and 3.5, respectively.
• the fluorine-based oil-repellent resin and polyvinyl alcohol are used at a ratio such that the amount of polyvinyl alcohol is normally 5 to 60 parts by mass, preferably 10 to 40 parts by mass, based on 100 parts by mass of the solid content of the fluorine-based oil-repellent resin.
• the polyvinyl alcohol used in the present invention may contain a functional group other than a hydroxyl group or acetate group.
• the functional group include an acetoacetyl group, a sulfonyl group, a sulfonyl base, a carboxyl group, a carboxyl base, a quaternary ammonium base, an oxyalkylene group, a polyoxyalkylene group, an alkyl group, an alkenyl group, an alkynyl group and a phenyl group.
• the solid content amount of the fluorine-based oil-repellent resin and polyvinyl alcohol fixed to the fiber is 0.2 to 1.0% by mass, preferably 0.4 to 0.8% by mass. It is preferable that the solid content amount is in a favorable range as described above because soil removal performance can be sufficiently exhibited, and the texture is soft.
• fluorine-based oil-repellent resin having a hydrophilic component and polyvinyl alcohol in addition to the fluorine-based oil-repellent resin having a hydrophilic component and polyvinyl alcohol, other resins, and agents such as compounds can be used in combination.
• a triazine ring-containing resin as the resin from the viewpoint of washing durability for soil resistant.
• the triazine ring-containing resin include melamine resins, guanamine resins and bismaleimide triazine resins, and melamine resins are particularly preferably used.
• the triazine ring-containing resin means a resin including a triazine ring-containing compound as a polymerization component, and the triazine ring-containing compound is a compound containing a triazine ring and having at least two polymerizable functional groups. Examples thereof include triazine ring-containing compounds represented by the following structural formula.
• ethylene urea copolymer compounds dimethylol urea copolymer compounds, dimethylol thiourea copolymer compounds, acid colloid compounds and the like of the above-described compounds can be used.
• the method for forming a triazine ring-containing resin is as follows. An aqueous liquid including the triazine ring-containing compound and a catalyst are added onto the fiber, heat treatment is carried out to perform polymerization.
• the catalyst to be used examples include acids such as acetic acid, formic acid, acrylic acid, malic acid, tartaric acid, maleic acid, phthalic acid, sulfuric acid, persulfuric acid, hydrochloric acid and phosphoric acid, and ammonium salts, sodium salts, potassium salts and magnesium salts of these acids, and one or more of these compounds can be used. Among them, ammonium persulfate and potassium persulfate are preferably used as the catalyst.
• the amount of the catalyst is preferably 0.1 to 20% by mass based on the amount of the monomer used.
• the heat treatment for such polymerization is preferably dry heat treatment and steaming heat treatment performed at a temperature of 50 to 200°C, preferably 80 to 150°C, for 0.1 to 30 minutes.
• the amount of the triazine ring-containing resin deposited is preferably 10 to 100% by mass, more preferably 20 to 60% by mass, based on the total weight of the fluorine-based oil-repellent resin having a hydrophilic component and polyvinyl alcohol.
• the soil resistant fiber structure of the present invention has a soil removability degree of preferably 3 to 4 or more, more preferably 4 or more, after industrial washing is performed 50 times after processing.
• Examples of the fiber raw material to be used in the soil resistant fiber structure of the present invention include synthetic fibers such as fibers composed of polyalkylene terephthalates such as polyethylene terephthalate, polypropylene terephthalate and polybutylene terephthalate; aromatic polyester-based fibers obtained by copolymerizing the above-mentioned resins with a third component; aliphatic polyester-based fibers composed of aliphatic polyester such as polylactic acid typified by one containing L-lactic acid as a main component; polyamide-based fibers composed of polyamides such as nylon 6 and nylon 66; acryl-based fibers containing polyacrylonitrile as a main component; polyolefin-based fibers composed of polyolefins such as polyethylene and polypropylene; polyvinyl chloride-based fiber; semisynthetic fibers such as acetate fiber and rayon fiber; and natural fibers such as cotton fiber, silk fiber and wool fiber.
• synthetic fibers such as fibers composed of poly
• one of these fibers can be used alone, or two or more of these fibers can also be used as a mixture.
• mixtures of natural fibers such as cotton fiber, silk fiber and wool fiber with fibers containing polyester-based fiber or polyamide-based fiber as a main component or fibers containing polyester-based fiber or polyamide-based fiber as a main component are preferably used.
• the main component refers to fiber, the content of which is the highest among the contained components.
• the main component is contained in an amount of 50% by mass or more.
• the fibers used in the soil resistant fiber structure of the present invention may be ordinary flat yarns, or filament yarns such as false-twisted yarns, twisted yarns, Taslan processed yarns, nanofibers, slub yarns and blended yarns, and various other modes of yarns such as staple fibers, tows and spun yarns can be used.
• filament yarns are used.
• the single fiber cross-sectional shape of the fiber used in the soil resistant fiber structure of the present invention is not particularly limited, and fibers in various forms such as circles, triangles, flat shapes and multilobal shapes can be used.
• fibers having a circular cross-sectional shape are preferably used.
• the soil resistant fiber structures of the present invention include fabric-like materials such as knitted fabrics, woven fabrics and nonwoven fabrics and string-like materials which are formed using the aforementioned fibers.
• fabric-like materials such as knitted fabrics, woven fabrics and nonwoven fabrics and string-like materials which are formed using the aforementioned fibers.
• knitted fabrics, woven fabrics and non-woven fabrics are used.
• a general processing agent such as a fluorescent dye or a softening agent may be added to the aforementioned fabric-like material or the string-like material.
• Fiber internally modified with an antibacterial agent or a bacteriostatic agent may be used as a raw material for the soil resistant fiber structure.
• processing agent examples include pyridine-based compounds such as 2-chloro-6-trichloromethylpyridine, 2-chloro-4-trichloromethyl-6-methoxypyridine, 2-chloro-4-trichloromethyl-6-(2-furylmethoxy)pyridine, di(4-chlorophenyl)pyridylmethanol, 2,3,5-trichloro-4-(n-propylsulfonyl)pyridine, 2-pyridylthiol-1-oxide zinc and di(2-pyridylthiol-1-oxide) can be used.
• pyridine-based compounds such as 2-chloro-6-trichloromethylpyridine, 2-chloro-4-trichloromethyl-6-methoxypyridine, 2-chloro-4-trichloromethyl-6-(2-furylmethoxy)pyridine, di(4-chlorophenyl)pyridylmethanol, 2,3,5-trichloro-4-(n-propyls
• fiber may be used on which a resin other than a fluorine-based oil-repellent resin having a hydrophilic component and polyvinyl alcohol, etc. (hereinafter, referred to correctively as a "soil resistant resin", and a film containing the resin is sometimes referred to as a "soil resistant resin layer”) is deposited.
• a resin layer other than the soil resistant resin layer is formed on the fiber, and the soil resistant resin layer is subsequently formed, so that two resin layers are present on the fiber.
• the resin other than the soil resistant resin include silicone resins, polyester resins, isocyanate compounds, epoxy resins, melamine resins, guanamine resins and bismaleimide triazine resins.
• fiber modified by crosslinking may be used, and as a crosslinking agent to be used for modification by crosslinking, a compound is preferably used which is capable of forming a crosslinked structure between cellulose molecules and in cellulose molecules by reacting with hydroxyl groups in cellulose molecules forming cellulose-based fiber, particularly hydroxyl groups present in amorphous regions that cause creases, loss of shape and shrinkage.
• fixation of the resin to the fiber structure can be performed by treating the fiber structure with a treatment liquid containing raw materials such as a soil resistant resin, a triazine ring-containing resin as an optional component or a polymerizable monomer for obtaining the triazine ring-containing resin, and a catalyst.
• a treatment liquid containing raw materials such as a soil resistant resin, a triazine ring-containing resin as an optional component or a polymerizable monomer for obtaining the triazine ring-containing resin, and a catalyst.
• Specific treatment methods include a pad-dry-cure method in which a fiber structure is immersed in a treatment liquid containing an soil resistant resin, squeezed with a certain pressure in a spread state, and then heat-treated; a pad-cure method in which a fiber structure is immersed in a treatment liquid containing an soil resistant resin, squeezed with a certain pressure in a spread state, and then heat-treated; a pad-steam method in which a fiber structure is immersed in the manner described above, and steaming heat treatment is then performed; and a bathing method in which a fiber structure is heated in a state of being immersed in a treatment liquid containing the above-described soil resistant resin.
• methods that are preferably used include a pad-dry-cure method in which a fiber structure is immersed in a treatment liquid containing an soil resistant resin, then squeezed with a certain pressure in a spread state, dried at a temperature of preferably 80 to 170°C, and then heat-treated at a temperature of preferably 170 to 200°C; a pad-cure method in which a fiber structure is instantaneously dried at a temperature of 170 to 200°C; a pad steam method in which steaming heat treatment is performed at a temperature of 80 to 110°C; and a bathing method in which a fiber structure is heated to a temperature of preferably 50 to 130°C in a state of being immersed in a treatment liquid containing the soil resistant resin.
• a pad-dry-cure method is most preferably used in which a fiber structure is dried at a temperature of 120°C to 170°C, and then heat-treated at 170 to 200°C.
• the soil resistant fiber structure thus obtained includes a resin film containing polyvinyl alcohol.
• oily soil difficult to wash out is inhibited from adhering to the fiber, and affinity with a washing liquid during washing is enhanced, so that the fiber structure has both adhesion suppressibility against aqueous soil and oily soil and soil removability even after being repeatedly washed after processing. Therefore, the soil-resistant fiber structure can be suitably used for general clothing, work uniforms, bedclothing, medical garments, interior articles, industrial material products and the like.
• the oil repellency degree ranges from 1 to 8, and a higher value shows higher oil repellency.
• the oil repellency degree is determined on the basis of assessment photographs attached to AATCC 118 method.
• the obtained twill woven fabric was refined at a temperature of 95°C by a continuous refining machine in accordance with a conventional method, rinsed with hot water, and then dried at a temperature of 130°C.
• the twill woven fabric was then dyed fluorescent-white at a temperature of 130°C using a jet dyeing machine, washed by a conventional manner, washed with hot water, dried, heated at a temperature of 170°C to obtain a white fabric having a warp density of 86/2.54 cm and a weft density of 55/2.54 cm.
• Components (A), (B), (H) and (I) as described later were then dissolved in amounts of 90 g/L, 18 g/L, 4.5 g/L and 0.75 g/L, respectively, to prepare a treatment liquid
• the white fabric prepared as described above was immersed in a spread state in the treatment liquid, squeezed to a squeezing ratio of 60% with a mangle, dried at a temperature of 130°C, and then heated at a temperature of 170°C to obtain a soil resistant fiber structure.
• the obtained soil resistant fiber structure had a pressed soil removability degree of 4 in soil gray scale determination after processing, and a pressed soil removability degree of 4 in soil gray scale determination after industrial washing was performed 50 times.
• Example 1 Except that with respect to Example 1, the amount of component (B) was 36 g/L, the same procedure as in Example 1 was carried out to obtain a soil resistant fiber structure.
• the obtained soil resistant fiber structure had a pressed soil removability degree of 4 in soil gray scale determination after processing, and a pressed soil removability degree of 3 to 4 in soil gray scale determination after industrial washing was performed 50 times.
• Example 1 Except that with respect to Example 1, component (C) was used in an amount of 18 g/L as polyvinyl alcohol, the same procedure as in Example 1 was carried out to obtain a soil resistant fiber structure.
• the obtained soil resistant fiber structure had a pressed soil removability degree of 3 to 4 in soil gray scale determination after processing, and a pressed soil removability degree of 3 to 4 in soil gray scale determination after industrial washing was performed 50 times.
• Example 1 Except that with respect to Example 1, component (D) was used in an amount of 18 g/L as polyvinyl alcohol, the same procedure as in Example 1 was carried out to obtain a soil resistant fiber structure.
• the obtained soil resistant fiber structure had a pressed soil removability degree of 3 to 4 in soil gray scale determination after processing, and a pressed soil removability degree of 3 in soil gray scale determination after industrial washing was performed 50 times.
• the obtained plain woven fabric was refined at a temperature of 95°C by a continuous refining machine in accordance with a conventional method, rinsed with hot water, and then dried at a temperature of 130°C.
• the plain woven fabric was then dyed fluorescent-white at a temperature of 130°C using a jet dyeing machine, washed by a conventional manner, washed with hot water, dried, heated at a temperature of 170°C to obtain a white fabric having a warp density of 138/2.54 cm and a weft density of 72/2.54 cm.
• Soil resistance processing was then performed in the same manner as in Example 1 to obtain a soil resistant fiber structure.
• the obtained soil resistant fiber structure had a pressed soil removability degree of 4 in soil gray scale determination after processing, and a pressed soil removability degree of 4 to 5 in soil gray scale determination after industrial washing was performed 50 times.
• Example 5 Except that with respect to Example 5, the amount of component (B) was 36 g/L, the same procedure as in Example 5 was carried out to obtain a soil resistant fiber structure.
• the obtained soil resistant fiber structure had a pressed soil removability degree of 4 to 5 in soil gray scale determination after processing, and a pressed soil removability degree of 4 in soil gray scale determination after industrial washing was performed 50 times.
• the obtained plain woven fabric was refined at a temperature of 95°C by a continuous refining machine in accordance with a conventional method, rinsed with hot water, and then dried at a temperature of 130°C.
• the plain woven fabric was then dyed fluorescent-white at a temperature of 130°C using a jet dyeing machine, washed by a conventional manner, washed with hot water, dried, heated at a temperature of 170°C to obtain a white fabric having a warp density of 115/2.54 cm and a weft density of 72/2.54 cm.
• Soil resistance processing was then performed in the same manner as in Example 1 to obtain a soil resistant fiber structure.
• the obtained soil resistant fiber structure had a pressed soil removability degree of 4 in soil gray scale determination after processing, and a pressed soil removability degree of 4 to 5 in soil gray scale determination after industrial washing was performed 50 times.
• Example 7 Except that with respect to Example 7, the amount of component (B) was 36 g/L, the same procedure as in Example 7 was carried out to obtain a soil resistant fiber structure.
• the obtained soil resistant fiber structure had a pressed soil removability degree of 4 in soil gray scale determination after processing, and a pressed soil removability degree of 4 to 5 in soil gray scale determination after industrial washing was performed 50 times.
• Example 1 Except that with respect to Example 1, the amount of component (B) was 54 g/L, the same procedure as in Example 1 was carried out to obtain a soil resistant fiber structure.
• the obtained soil resistant fiber structure had a pressed soil removability degree of 4 to 5 in soil gray scale determination after processing, and a pressed soil removability degree of 2 to 3 in soil gray scale determination after industrial washing was performed 50 times.
• Example 1 Except that with respect to Example 1, component (E) was used in an amount of 90 g/L as a fluorine-based oil-repellent resin, the same procedure as in Example 1 was carried out to obtain a soil resistant fiber structure.
• the obtained soil resistant fiber structure had a pressed soil removability degree of 3 to 4 in soil gray scale determination after processing, and a pressed soil removability degree of 2 to 3 in soil gray scale determination after industrial washing was performed 50 times.
• Example 1 Except that with respect to Example 1, component (B) was not used, the same procedure as in Example 1 was carried out to obtain a low-water-repellent and oil-repellent soil resistant fiber structure.
• the obtained soil resistant fiber structure had a pressed soil removability degree of 2 to 3 in soil gray scale determination after processing, and a pressed soil removability degree of 3 to 4 in soil gray scale determination after industrial washing was performed 50 times.
• Example 1 Except that with respect to Example 1, component (A) was not used, the same procedure as in Example 1 was carried out to obtain a fiber structure.
• the obtained soil resistant fiber structure had a pressed soil removability degree of 1 to 2 in soil gray scale determination after processing, and a pressed soil removability degree of 2 in soil gray scale determination after industrial washing was performed 50 times.
• component (E) was used in an amount of 90 g/L as a fluorine-based oil-repellent resin, the same procedure as in Comparative Example 1 was carried out to obtain a water-absorbing soil resistant fiber structure.
• the obtained soil resistant fiber structure had a pressed soil removability degree of 3 to 4 in soil gray scale determination after processing, and a pressed soil removability degree of 2 to 3 in soil gray scale determination after industrial washing was performed 50 times. Pressed soil spread over a larger area as compared to Example 8.
• the white fabric obtained in Example 1 was immersed in a treatment liquid prepared by dissolving components (F), (H) and (J) in amounts of 45 g/L, 15 g/L and 3.0 g/L, respectively, and the white fabric was squeezed to a squeezing ratio of 60% using a mangle, and treated in a saturated water vapor atmosphere at 105°C for 5 minutes.
• the white fabric was then washed in an aqueous solution containing sodium carbonate at 1 g/L at 60°C for 1 minute, rinsed with water, dried at a temperature of 130°C, and then heated at a temperature of 170°C to obtain a soil resistant fiber structure.
• the obtained soil resistant fiber structure had a pressed soil removability degree of 3 in soil gray scale determination after processing, and a pressed soil removability degree of 3 in soil gray scale determination after industrial washing was performed 50 times.
• component (G) was used in an amount of 90 g/L instead of fluorine-based oil-repellent resin (A), the same procedure as in Comparative Example 1 was carried out to obtain a water-absorbing and oil-absorbing soil resistant fiber structure.
• the obtained soil resistant fiber structure had a pressed soil removability degree of 2 to 3 in soil gray scale determination after processing, and a pressed soil removability degree of 2 to 3 in soil gray scale determination after industrial washing was performed 50 times.
• Table 2 shows the compositions of the treatment liquids (A) to (J) and the results of performance etc. of obtained fiber structures in Examples 1 to 8 and Comparative Examples 1 to 5.
• Table 2 shows the compositions of the treatment liquids (A) to (J) and the results of performance etc. of obtained fiber structures in Examples 1 to 8 and Comparative Examples 1 to 5.
• Example 1 Example 2
• Example 3 Example 4
• Example 5 Example 6
• Example 7 Example 8
• Example 9 Example 10 With soil resistance Composi tion of treatment liquid (g/L)
• Table 2 reveals that in each of Examples 1 to 10 as the fiber structures of the present invention, pressed soil was easily repelled, an area over which soil spread was small, and soil hardly adhered. In addition, excellent soil removability against pressed soil was exhibited. On the other hand, in Comparison Examples 1 to 5 as soil resistant fiber structures different from those of the present invention, soil removability against pressed soil was lower as compared to examples. It was possible to improve washing durability for soil resistance in Example 9 where a larger amount of polyvinyl alcohol was added, or by optimizing the amount of polyvinyl alcohol added. By improving washing durability, the functionality can be maintained even after repeated washing, and the life of clothing can be extended.
• the soil resistant fiber structure of the present invention has both high adhesion suppressibility against aqueous soil and oily soil and soil removability in washing, and is therefore suitably used for general clothing, work uniforms, bedclothing, medical garments, interior articles, industrial material products and the like.
• the soil resistant fiber structure is suitably used as a work uniform which is apt to suffer adhesion of oily soil difficult to wash out, and thus needs to have soil resistance performance.

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• 2018
  • 2018-10-04 EP EP18866556.6A patent/EP3696318A4/de not_active Withdrawn
  • 2018-10-04 JP JP2018553493A patent/JPWO2019073898A1/ja active Pending
  • 2018-10-04 KR KR1020207008886A patent/KR20200058418A/ko not_active Application Discontinuation
  • 2018-10-04 WO PCT/JP2018/037209 patent/WO2019073898A1/ja unknown
  • 2018-10-04 US US16/645,186 patent/US20200283949A1/en not_active Abandoned
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• 2023
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