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
  • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
  • D06M13/244—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus
  • D06M13/282—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus with compounds containing phosphorus
  • D06M13/292—Mono-, di- or triesters of phosphoric or phosphorous acids; Salts thereof
  • D06M13/295—Mono-, di- or triesters of phosphoric or phosphorous acids; Salts thereof containing polyglycol moieties; containing neopentyl moieties
• • 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
  • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
  • D06M13/02—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with hydrocarbons
• • 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
  • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
  • D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
  • D06M13/224—Esters of carboxylic acids; Esters of carbonic acid
• • 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
  • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
  • D06M13/244—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus
  • D06M13/282—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus with compounds containing phosphorus
  • D06M13/292—Mono-, di- or triesters of phosphoric or phosphorous acids; Salts thereof
• • 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

Definitions

• the present invention relates to a fiber treatment agent for nonwoven fabrics and a nonwoven fabric using the same.
• the hydrophilic capacity is often controlled by the proportion of the alkyl chain length in the blending base agent; to improve hydrophilic capacity and processing suitability, it is necessary to blend a large amount of a phosphate ester salt or the like with a short alkyl chain length.
• a phosphate ester salt with a short alkyl chain length is a strong hydrophilizing base agent, and the action of the phosphate ester salt being held on hydrophobic fibers is temporary; hence, when the hydrophilizing agent is provided with water, most of the hydrophilizing agent is typically washed away.
• Patent Literatures 1 to 8 attention is not focused on the issue of suppressing the transfer of the chemical agent; and there has been desired a technology in which conventionally required hydrophilicity and repeated water permeability are satisfied and yet the transfer of, to an unintentional part, the chemical agent attached by treatment to fibers is suppressed, particularly a technology in which, even when a strong hydrophilizing base agent is used, another place in an article is prevented from being contaminated.
• the present invention has been made in view of the circumstances described above, and an issue of the present invention is to provide a fiber treatment agent for nonwoven fabrics by which hydrophilicity and repeated water permeability can be imparted to a nonwoven fabric and yet the transfer to another part in an article using the nonwoven fabric can be suppressed.
• the present inventor conducted extensive studies in order to solve the issue mentioned above, and has found out that a fiber treatment agent for nonwoven fabrics excellent in hydrophilicity and the suppression of transfer by which, even when an alkyl phosphate ester salt or the like that imparts hydrophilicity, particularly a phosphate ester salt with a short alkyl chain length, is used, transfer from a nonwoven fabric to another part is less likely to occur is obtained by using a polyhydric alcohol fatty acid ester or the like with a melting point of more than or equal to 15°C; thus, has completed the present invention.
• a fiber treatment agent for nonwoven fabrics includes: components (A) and (B) below:
• a nonwoven fabric wherein fibers are subjected to attachment treatment with the fiber treatment agent for nonwoven fabrics.
• hydrophilicity and repeated water permeability can be imparted to a nonwoven fabric, permeability to fibers is provided, and transfer to another part in an article using the nonwoven fabric can be suppressed.
• a fiber treatment agent for nonwoven fabrics as a hydrophilizing agent used for hygienic material uses or the like
• the control of the speed of water absorption is essential in view of quickening surface absorption, causing the fiber treatment agent to arrive at high-absorbent resin or the like, etc., and also repeated water permeability (durability) is regarded as important; hence, it is inevitably essential to blend a hydrophilizing base agent with strong hydrophilicity; however, a mechanism by which another place is prevented from being contaminated even when such a base agent is used is needed.
• an alkyl phosphate ester salt or the like of component (A), which is a temporary hydrophilizing agent that is, when used singly, mostly washed away upon being provided with water, is allowed to be slowly released by using, as component (B), a polyhydric alcohol fatty acid ester or the like with a melting point of more than or equal to 15°C.
• component (A) When the fiber treatment agent for nonwoven fabrics is attached by treatment to fibers, component (A) is oriented on a surface of the fibers such that a hydrophilic portion of the molecular structure of component (A) is on the front surface and a hydrophobic portion on the back surface; it is presumed that component (B) as a hydrophobic wax having a melting point of more than or equal to a certain degree of temperature holds the hydrophobic portion of component (A) on the surface of the hydrophobic fibers.
• the fiber treatment agent is, when provided with water, gradually locally washed away by the action of component (B) holding component (A), therefore acts as a hydrophilizing agent having light durability, and can thereby suppress transfer to another part in an article using the nonwoven fabric.
• the suppression of transfer is based on the following as a main standard: for example, the rate of decrease in water pressure resistance with a blank value as a standard being within 30%, particularly within 20%, and most preferably 10% in a measurement method described in Examples, i.e., water pressure resistance measurement using a measurement apparatus according to Method A (a low water pressure method) of the water resistance test (the hydrostatic pressure method).
• the fiber treatment agent is suitable for the exhibition of the effect of suppressing an event in which the chemical agent attached by treatment to fibers is transferred to an unintentional part and the performance and quality of the article are impaired.
• Component (A) used for the fiber treatment agent for nonwoven fabrics of the present invention is at least one selected from an alkyl phosphate ester salt and a polyoxyalkylene alkyl ether phosphate ester salt.
• Component (A) contains, as a main component, a phosphate monoester salt and/or a phosphate diester salt represented by Formula (I) below, and is preferably one containing a phosphate monoester salt in a largest amount.
• component (A) may contain a polyphosphate or the like.
• Component (A) is typically a mixture of these. [Chem.
• R represents an alkyl group
• AO represents an oxyalkylene group (A represents an alkylene part)
• M represents a cation
• m represents the average addition mole number of a polyoxyalkylene
• n represents an integer of 1 or 2.
• R's and M's may each be the same or mutually different.
• AOs may be the same or mutually different.
• Component (A) that is a mixture of a phosphate monoester salt, a phosphate diester salt, and the like can be obtained by, for example, reacting together an alkyl alcohol or a polyoxyalkylene alkyl ether having the corresponding alkyl group and phosphoric acid anhydride, and neutralizing the resulting alkyl phosphate ester or the resulting polyoxyalkylene alkyl ether phosphate with an alkali such as potassium hydroxide.
• the number of carbon atoms of the alkyl group in component (A) is not particularly limited, but is preferably 4 to 22 and more preferably 6 to 18.
• alkyl group examples include a butyl group, a hexyl group, an octyl group, a 2-ethylhexyl group (an isooctyl group), a nonyl group, a decyl group, an undecyl group, a dodecyl group (a lauryl group), a tridecyl group, a tetradecyl group, a pentadecyl group, a hexadecyl group, a heptadecyl group, an octadecyl group (a stearyl group), a nonadecyl group, an icosyl group, a henicosyl group, a docosyl group, and the like.
• Component (A) may be a mixture of compounds having mutually different alkyl groups; in this case, the number of carbon atoms of the alkyl group mentioned above is the average number of carbon atoms.
• Each of the butyl group to the docosyl group mentioned above includes various isomers such as an n-type, a sec-type, a tert-type, and a multi-branched type (an isotype).
• the oxyalkylene group in the polyoxyalkylene alkyl ether phosphate ester salt among a variety of components (A) preferably has 2 to 4 carbon atoms, more preferably 2 to 3 carbon atoms, and still more preferably 2 carbon atoms. Among them, the oxyalkylene groups may be the same or mutually different.
• the oxyalkylene groups preferably include an oxyethylene group as a whole. Among them, one in which all the oxyalkylene groups are solely oxyethylene groups and one in which an oxyethylene group and an oxypropylene group coexist are more preferable, and one in which all the oxyalkylene groups are solely oxyethylene groups is still more preferable.
• the average addition mole numbers m of the polyoxyalkylenes are mutually independently more than or equal to 0.25, more than or equal to 0.5, more than or equal to 1, or more than or equal to 2, for example. Further, the average addition mole numbers m of the polyoxyalkylenes are mutually independently less than or equal to 30, less than or equal to 20, less than or equal to 10, or less than or equal to 6, for example.
• the cation M in component (A) is not particularly limited, and examples include hydrogen, an alkali metal, an alkaline earth metal, magnesium, an organic ammonium, and the like.
• Examples of the alkali metal include lithium, sodium, potassium, and the like.
• Examples of the alkaline earth metal include calcium and the like.
• Examples of the organic ammonium include one represented by NR 1 R 2 R 3 R 4 .
• R 1 to R 4 mutually independently represent a hydrogen atom, an alkyl group or an alkylene group optionally having a hydroxy group, or a polyoxyalkylene group.
• alkali metal selected from sodium and potassium, ammonium, and an organic ammonium having an alkyl group or a hydroxyalkyl group having less than or equal to 20 carbon atoms, preferably less than or equal to 10 carbon atoms, and more preferably less than or equal to 5 carbon atoms are preferable.
• Component (A) may use component (A1) below.
• (A1) an alkyl phosphate ester salt or a polyoxyalkylene alkyl ether phosphate ester salt in which the number of carbon atoms of an alkyl group is 6 to 10.
• the fiber treatment agent for nonwoven fabrics of the present invention preferably contains component (A1).
• Component (A1) can enhance hydrophilicity, particularly the initial water permeability, and permeability to fibers necessary for the ensuring of processing suitability etc.
• the content amount of component (A1) is preferably more than or equal to 10 mass%, more preferably more than or equal to 20 mass%, still more preferably more than or equal to 30 mass%, particularly preferably more than or equal to 35 mass%, and most preferably more than or equal to 40 mass% relative to component (A).
• alkyl phosphate ester salt examples include a hexyl phosphate ester salt, an octyl phosphate ester salt, a 2-ethylhexyl phosphate ester salt, a decyl phosphate ester salt, an isodecyl phosphate ester salt, and the like.
• Examples of the polyoxyalkylene alkyl ether phosphate ester salt among a variety of components (A1) include a polyoxyethylene hexyl ether phosphate ester salt (POE(1) to POE(30)), a polyoxyethylene octyl ether phosphate ester salt (POE(1) to POE(30)), a polyoxyethylene 2-ethylhexyl ether phosphate ester salt (POE(1) to POE(30)), a polyoxyethylene decyl ether phosphate ester salt (POE(1) to POE(30)), a polyoxyethylene isodecyl ether phosphate ester salt (POE(1) to POE(30)), and the like.
• the number in the parentheses indicates the number of polyoxyethylene (POE) units.
• component (A2) an alkyl phosphate ester salt or a polyoxyalkylene alkyl ether phosphate ester salt in which the number of carbon atoms of an alkyl group is more than or equal to 11.
• Component (A2) controls hydrophilicity, enhances repeated water permeability, and can suppress transfer.
• component (A) preferably further contains component (A2) in addition to (A1), and thereby a fiber treatment agent for nonwoven fabrics excellent in balance between hydrophilicity, repeated water permeability, permeability to fibers, and the suppression of transfer can be obtained.
• the content amount of component (A2) is preferably less than or equal to 90 mass%, more preferably less than or equal to 80 mass%, still more preferably less than or equal to 70 mass%, particularly preferably less than or equal to 65 mass%, and most preferably less than or equal to 60 mass% relative to component (A).
• the content amount of component (A2) is preferably more than or equal to 10 mass%, more preferably more than or equal to 15 mass%, and still more preferably more than or equal to 20 mass%.
• alkyl phosphate ester salt among a variety of components (A2) include a dodecyl phosphate ester salt (a lauryl phosphate ester salt), a tridecyl phosphate ester salt, an isotridecyl phosphate ester salt, a tetradecyl phosphate ester salt (a myristyl phosphate ester salt), a hexadecyl phosphate ester salt (a cetyl phosphate ester salt), an octadecyl phosphate ester salt (a stearyl phosphate ester salt), an isooctadecyl phosphate ester salt (an isostearyl phosphate ester salt), and the like.
• a dodecyl phosphate ester salt a lauryl phosphate ester salt
• a tridecyl phosphate ester salt an isotridecyl phosphate ester salt
• Examples of the polyoxyalkylene alkyl ether phosphate ester salt among a variety of components (A2) include a polyoxyethylene dodecyl ether phosphate ester salt (a lauryl ether phosphate ester salt) (POE(1) to POE(30)), a polyoxyethylene tridecyl ether phosphate ester salt (POE(1) to POE(30)), a polyoxyethylene isotridecyl ether phosphate ester salt (POE(1) to POE(30)), a polyoxyethylene tetradecyl ether phosphate ester salt (a myristyl ether phosphate ester salt) (POE(1) to POE(30)), a polyoxyethylene hexadecyl ether phosphate ester salt (a cetyl ether phosphate ester salt) (POE(1) to POE(30)), a polyoxyethylene octadecyl ether phosphate ester salt (a stearyl
• Component (B) used for the fiber treatment agent for nonwoven fabrics of the present invention is at least one selected from a polyhydric alcohol fatty acid ester, a polyoxyalkylene polyhydric alcohol fatty acid ester, and a naturally derived wax each having a melting point of more than or equal to 15°C (hereinafter, also referred to as a wax component).
• Component (B) suppresses the transfer of component (A).
• the melting point of component (B) is more than or equal to 15°C, preferably more than or equal to 20°C, more preferably more than or equal to 25°C, and still more preferably more than or equal to 30°C.
• the melting point of component (B) is preferably less than or equal to 90°C, more preferably less than or equal to 80°C, still more preferably less than or equal to 70°C, and particularly preferably less than or equal to 60°C.
• component (B1) with a melting point of more than or equal to 60°C, particularly more than or equal to 80°C, is used, in view of enhancing permeability
• component (B1) is preferably used in combination with component (B2) with a melting point of less than 60°C, and the mass ratio (B1/B2)
• component (B1) to component (B2) is preferably less than 1.
• Each of the polyhydric alcohol fatty acid ester and the polyoxyalkylene polyhydric alcohol fatty acid ester among a variety of components (B) may be a monoester, a diester, a triester, or the like.
• the polyhydric alcohol of the polyhydric alcohol fatty acid ester and the polyoxyalkylene polyhydric alcohol fatty acid ester is a dihydric or higher alcohol, and is preferably a trihydric or higher alcohol. Further, the polyhydric alcohol is preferably a decahydric or lower alcohol, and more preferably an octahydric or lower alcohol.
• glycerin polyglycerin such as diglycerin
• sugar alcohol-based compounds such as trimethylolethane, trimethylolpropane, trimethylolbutane, ditrimethylolpropane, pentaerythritol, dipentaerythritol, sorbitan, erythritol, D-threitol, L-arabinitol, ribitol, xylitol, sorbitol, mannitol, galactitol, and rhamnitol, monosaccharides such as arabinose, ribose, xylose, glucose, mannose, galactose, fructose, sorbose, rhamnose, fucose, and ribodesose, disaccharides such as trehalose, sucrose, maltose, cellobiose, gentiobiose, lactose, and melibio
• the fatty acid of the polyhydric alcohol fatty acid ester and the polyoxyalkylene polyhydric alcohol fatty acid ester is not particularly limited; however, in view of the melting point etc., the number of carbon atoms of the fatty acid is preferably more than or equal to 8, and more preferably more than or equal to 12. Further, the number of carbon atoms is preferably less than or equal to 30, more preferably less than or equal to 22, and still more preferably less than or equal to 18.
• the fatty acid may be a saturated fatty acid, or may be an unsaturated fatty acid; among these, in view of enhancing the melting point etc., a saturated fatty acid is preferable, and a straight-chain saturated fatty acid is more preferable. Examples of the saturated fatty acid include caprylic acid, pelargonic acid, capric acid, lauric acid, myristic acid, palmitic acid, stearic acid, arachidic acid, behenic acid, and the like.
• the polyhydric alcohol fatty acid ester may be an oil or a fat obtained from nature, or a hardened oil or fat in which hydrogen is added.
• the average addition mole number of the polyoxyalkylene in the polyoxyalkylene polyhydric alcohol fatty acid ester among a variety of components (B) is, for example, less than or equal to 100 or less than or equal to 80 per molar equivalent of the hydroxyl group of the polyhydric alcohol ester.
• the oxyalkylene group preferably has 2 to 4 carbon atoms, and more preferably has 2 carbon atoms (an oxyethylene group) or 3 carbon atoms (an oxypropylene group).
• Examples of the naturally derived wax among a variety of components (B) include plant-based waxes, animal-based waxes, mineral-based waxes, and the like.
• Examples of the plant-based wax include carnauba wax, candelilla wax, rice bran wax, sumac wax, jojoba oil, and the like.
• Examples of the animal-based wax include lanoline, bees wax, spermaceti wax, and the like.
• As the mineral-based wax, paraffin wax, microcrystalline wax, petrolatam, ozokerite, ceresin, and the like are given.
• plant-based waxes are preferable. Any of these may be used singly, or two or more of these may be used in combination.
• the mass ratio (B)/(A) of component (B) to component (A) is preferably less than 1 in view of enhancing hydrophilicity. Further, in view of suppressing transfer, the mass ratio (B)/(A) is preferably more than or equal to 0.1, more preferably more than or equal to 0.2, and still more preferably more than or equal to 0.3.
• the fiber treatment agent for nonwoven fabrics of the present invention has the effect of the present invention, that is, hydrophilicity, repeated water permeability, and permeability to fibers; in view of enabling the suppression of transfer, the total amount of components (A) and (B) is preferably more than or equal to 50 mass%, more preferably 60 mass%, still more preferably more than or equal to 70 mass%, particularly preferably more than or equal to 80 mass%, and most preferably more than or equal to 85 mass% relative to the solid content of the fiber treatment agent for nonwoven fabrics.
• the solid content is the proportion excluding water and volatile components such as solvent that disappear when the fiber treatment agent is attached by treatment to fibers.
• penetrant (C) may be blended for the purpose of improving the capacity of permeation to fibers, in addition to components (A) and (B).
• penetrant (C) nonionic surfactants such as a polyoxyalkylene alkyl ether, anionic surfactants such as a polyoxyalkylene alkyl ether sulfate and a sulfosuccinic acid ester salt, polyether-modified silicones, and the like are given.
• a polyoxyalkylene alkyl ether particularly a polyoxyalkylene branched alkyl ether, is preferably used because permeation capacity can be improved inexpensively.
• the blending amount of the penetrant is preferably less than or equal to 20 mass%, more preferably less than or equal to 15 mass%, and still more preferably less than or equal to 10 mass% relative to the solid content of the fiber treatment agent for nonwoven fabrics. Any of these may be used singly, or two or more of these may be used in combination.
• the alkyl portion in the polyoxyalkylene alkyl ether may be a straight-chain alkyl group or a branched-chain alkyl group, and is preferably an alkyl group having 8 to 14 carbon atoms, and more preferably an alkyl group having 10 to 12 carbon atoms.
• Examples of the branched-chain alkyl group include an isooctyl group, an isodecyl group, an isododecyl group, an isohexadecyl (isocetyl) group, an isooctadecyl (isostearyl) group, an octyldodecyl group, a decyltetradecyl group, and the like.
• the average addition mole number of the polyoxyalkylene in each of the polyoxyalkylene straight-chain alkyl ether and the polyoxyalkylene branched alkyl ether is preferably 2 to 12, and more preferably 4 to 8.
• the oxyalkylene group preferably has 2 to 4 carbon atoms, and more preferably has 2 carbon atoms (an oxyethylene group) or 3 carbon atoms (an oxypropylene group).
• a plurality of kinds having different numbers of carbon atoms coexist among the oxyalkylene groups for example in the case where an oxyethylene group and an oxypropylene group coexist, these may coexist in a random manner, or may coexist in a block manner.
• the fiber treatment agent for nonwoven fabrics of the present invention may contain water or a solvent, and preferably contains water, as necessary.
• the water used for the present invention may be any of pure water, distilled water, purified water, soft water, ion-exchanged water, tap water, and the like.
• the proportion of the solid content at the time of manufacturing the fiber treatment agent for nonwoven fabrics of the present invention is preferably 5 to 90 mass%, and more preferably 10 to 80 mass%.
• the fiber treatment agent for nonwoven fabrics of the present invention may contain other components as well as the components mentioned above to the extent that the effect of the present invention is not impaired.
• the other component include a surfactant, an antibacterial agent, an antioxidant, an antiseptic agent, a matting agent, a pigment, an antirust agent, an aromatic, an antifoaming agent, a perfume, a pH adjuster, a viscosity adjuster, etc.
• the surfactant examples include nonionic surfactants such as a polyoxyalkylene alkyl ether, a polyoxyalkylene alkenyl ether, a polyoxyalkylene fatty acid ester, and a fatty acid alkanolamide, anionic surfactants such as an alpha-olefin sulfonate, an alkylbenzene sulfonate, an alkyl sulfate, a polyoxyalkylene alkyl ether sulfate, and a sulfosuccinic acid ester salt, amphoteric surfactants such as an alkyl betaine, an alkyl sulfobetaine, and an alkylamino fatty acid salt, cationic surfactants such as an alkyl quaternary ammonium salt, and the like.
• anionic surfactants such as an alpha-olefin sulfonate, an alkylbenzene sulfonate, an alkyl
• the dynamic surface tension at the time of a bubble lifetime according to the maximum bubble pressure method of 100 milliseconds in an aqueous solution prepared such that the solid content is 2 mass% is preferably less than or equal to 55 mN/m, and more preferably less than or equal to 50 mN/m.
• the fiber treatment agent has good permeability to hydrophobic fibers, does not inhibit process transitability, and is suitable for the exhibition of the effect of suppressing transfer.
• the method for manufacturing the fiber treatment agent for nonwoven fabrics of the present invention is not particularly limited; for example, the fiber treatment agent for nonwoven fabrics of the present invention can be obtained by blending together components (A) and (B) and water, blending component (C) and other components as necessary, and uniformly mixing the components at normal temperature or, as necessary, by heating (for example, 40 to 100°C).
• the blending order and the blending method of the components are not particularly limited.
• the fiber treatment agent for nonwoven fabrics of the present invention can, for example, be provided to fibers as an emulsion dispersion liquid, which may be obtained by diluting the fiber treatment agent for nonwoven fabrics of the present invention with water, as necessary.
• Examples of the source material fibers of the nonwoven fabric include polyolefin fibers such as polyethylene and polypropylene, synthetic fibers such as polyester fibers and polyamide fibers, regenerated fibers such as rayon and cuprammonium rayon, natural fibers such as cotton, and the like, and mixing fibers, composite fibers, and the like using two or more of these.
• the cross-sectional form of the fiber As the cross-sectional form of the fiber, a circular cross section, a deformed cross section, and the like are given.
• the deformed cross section include a star shape, an ellipse, a triangle, a quadrangle, a pentagon, a multifoliate shape, a dumbbell shape, a T-shaped form, a horseshoe shape, and the like.
• Examples of the cross-sectional form of the composite fiber include a sheath-core form, a parallel form, an eccentric sheath-core form, a multilayer form, a radial form, a sea-island form, and the like.
• Examples of the composite fiber include polyolefin resin/polyolefin resin such as high-density polyethylene/polypropylene, straight-chain-form low-density polyethylene/polypropylene, low-density polyethylene/polypropylene, a binary copolymer or a ternary copolymer of propylene and other ⁇ -olefins/polypropylene, straight-chain-form low-density polyethylene/high-density polyethylene, and low-density polyethylene/high-density polyethylene, polyolefin resin/polyester resin such as polypropylene/polyethylene terephthalate, high-density polyethylene/polyethylene terephthalate, straight
• the method for spinning source material fibers may be a known spinning method, and examples include the melt spinning method, the wet spinning method, the dry spinning, and the like.
• the spun fibers may be subjected to processing such as stretching or crimping.
• Examples of the method for forming an accumulation layer of fibers include the dry method, the wet method, the spun bonding method, and the like.
• the dry method is a method in which short fibers (for example, 15 to 100 mm) are arranged in a fixed direction or randomly with a carding machine or an air flow called an air lay and an accumulation layer of fibers is formed.
• the wet method is a method in which short fibers are dispersed in water and are fashioned into a thin layer with a paper machine to form an accumulation layer of fibers.
• the spun bonding method is a method in which a melted source material resin is melted out and spun from the tip of a nozzle of a spinning machine and an accumulation layer of fibers is formed with continuous long fibers.
• the melt blowing method, the flash spinning method, and the like are given as well as the above.
• Examples of the method for bonding fibers together include the thermal bonding method, the needle punching method, the hydroentanglement method, the chemical bonding method, and the like.
• the thermal bonding method is a method in which an accumulation layer of fibers in which low-melting-point thermal fusion bonding fibers are mixed is passed between hot rolls to be thermocompression-bonded, or hot air is applied to adhere fibers together.
• the needle punching method is a method in which an accumulation layer of fibers is repeatedly stuck with needles vertically moving at high speed and protrusions cut in the needles are used to entangle fibers together.
• the hydroentanglement method is also called spun lacing, water punching, and water jetting, and is a method in which high-pressure water flows are jetted to an accumulation layer of fibers to entangle fibers together.
• the chemical bonding method is a method in which an emulsion-based adhesive resin is attached to an accumulation layer of fibers by a method such as impregnation or spraying, and heating and drying are performed to adhere intersection points of fibers together.
• the method for performing the attachment treatment of the fiber treatment agent for nonwoven fabrics of the present invention to fibers is not particularly limited.
• the fiber treatment agent for nonwoven fabrics of the present invention may be supplied as a spinning oil agent or a process oil agent designed for the streamlining, facilitation, or the like of the manufacturing process, or a finish oil agent designed for an effect for the end use.
• a process oil agent also performances such as antistatic capacity, smoothness, durability, thermal stability, and safety, which suppress the occurrence of static electricity due to friction caused by a carding machine or the like, the tearing of fibers, the occurrence of pilling, etc., can be imparted.
• Examples of the process of attaching the fiber treatment agent for nonwoven fabrics of the present invention to fibers include processes such as spinning, stretching, and crimping.
• As the attachment method for example, a method in which the fiber treatment agent for nonwoven fabrics of the present invention is supplied to fibers by a means such as oil supply with rollers, immersion, spraying, or foam coating and drying is performed, etc. are given as means for obtaining the target attachment amount in a uniform way with good efficiency in accordance with the manufacturing process and the characteristics of fibers.
• attachment treatment may be performed by a method in which the fiber treatment agent for nonwoven fabrics of the present invention is supplied to a nonwoven fabric in which fibers are bonded together by, for example, a means such as oil supply with rollers, immersion, spraying, or foam coating and drying is performed.
• the attachment amount of the fiber treatment agent for nonwoven fabrics of the present invention to fibers is not particularly limited; however, in view of obtaining the effect of the present invention, performance as a process oil agent, etc., the attachment amount is preferably 0.05 to 2 mass% and more preferably 0.1 to 1.5 mass% as the solid content, with the mass of fibers as a standard.
• the nonwoven fabric of the present invention is one in which fibers are subjected to attachment treatment with the fiber treatment agent for nonwoven fabrics of the present invention.
• the nonwoven fabric has hydrophilicity, repeated water permeability, and permeability to fibers, and can suppress transfer; thus, can be used for various uses in which such performance is required. Examples of fields in which the nonwoven fabric of the present invention can be used include hygienic material uses, medical uses, clothing uses, daily goods, agriculture and public works material uses, matrices for tapes, filter uses, wrapping material uses, and the like.
• the nonwoven fabric is suitable for fields in which not only the impartment of hydrophilicity etc.
• the nonwoven fabric is suitable for a surface material, for example the top sheet, an intermediate sheet placed between the top sheet and an absorbent element, or the like, of an absorbent article such as a paper diaper such as a baby disposable diaper or a disposable diaper for nursing care, or a sanitary item such as a napkin.
• a surface material for example the top sheet, an intermediate sheet placed between the top sheet and an absorbent element, or the like, of an absorbent article such as a paper diaper such as a baby disposable diaper or a disposable diaper for nursing care, or a sanitary item such as a napkin.
• a nonwoven fabric for evaluation made of polypropylene was produced by the following method.
• Each of the fiber treatment agents for nonwoven fabrics of Examples and Comparative Examples was diluted in water at 40°C such that the solid content was 1 mass%, and a dilute liquid was obtained.
• a polypropylene spun-bonded nonwoven fabric with a mass per unit area of 20 g/m 2 was immersed in the dilute liquid to be supplied with oil, compression was performed such that the target attachment amount of oil of the nonwoven fabric was 0.6 mass%, and then drying was performed with a dryer at 80°C for 30 minutes; thus, a nonwoven fabric was obtained.
• alkyl phosphate ester salts or derivatives A
• wax components B
• penetrants C
• the blending amount described in Table 1 shows the effective content.
• the melting point of wax component (B) was measured with a minute amount melting point measurement apparatus (MP-3S, manufactured by Yanaco Kikikaihatsu Kenkyusho K.K.).
• MP-3S minute amount melting point measurement apparatus
• the chemical agent refers to the fiber treatment agent for nonwoven fabrics of each of Examples and Comparative Examples
• the attachment amount refers to the attachment amount of the solid content (the total effective content) except water of the chemical agent.
• the case where the penetration time of the physiological saline solution was within 10 seconds was classified as ⁇ +, the case where the penetration time was more than 10 seconds and within 30 seconds as ⁇ , the case of more than 30 seconds and within 1 minute as o, the case of more than 1 minute and within 2 minutes as ⁇ , and the case of more than 2 minutes as ⁇ .
• the evaluation was performed by measuring places where the waterdrop soaked within 3 seconds; the case of more than or equal to 8 places was classified as ⁇ , the case of 7 or 6 places as o, the case of 5 to 2 places as ⁇ , and the case of less than or equal to 1 place as ⁇ .
• a 2-mass% aqueous solution (on an effective content basis) of a chemical agent to be evaluated was prepared, a nonwoven fabric for evaluation made of chemical-agent-untreated polypropylene cut out in a 10-cm square (mass per unit area: 20 g/m 2 ) was gently dropped from above the aqueous solution, and the time until the aqueous solution permeated through the entire nonwoven fabric was measured.
• the case where the time until the bath liquid permeated through the entire nonwoven fabric was within 5 seconds was classified as ⁇ , the case of more than 5 seconds and within 10 seconds as o, the case of more than 10 seconds and within 15 seconds as ⁇ , and the case of more than 15 seconds as ⁇ .
• a 2-mass% aqueous solution (on an effective content basis) of a chemical agent to be evaluated was prepared, the measurement of the maximum bubble pressure method was performed by using a commercially available dynamic surface tension measurement apparatus (BP-D5, manufactured by Kyowa Interface Science Co., Ltd), and the surface tension (mN/m) at the time of a bubble lifetime of 100 milliseconds (msec) was recorded as a measurement value.
• BP-D5 dynamic surface tension measurement apparatus
• Method A a low water pressure method of the water resistance test (the hydrostatic pressure method) described in JIS L 1092:2009, "Testing methods for water resistance of textiles”.
• the test piece was placed in the measurement apparatus such that the contact surface with the chemical-agent-treated nonwoven fabric was located on the side of the water-contact surface.
• the water pressure resistance measurement of a chemical-agent-untreated nonwoven fabric was performed before the test, and the measurement value was used as a blank value.
• the case where the rate of decrease in water pressure resistance of the test piece was within 10% of the blank value was classified as ⁇ +, the case of more than 10% and within 20% as ⁇ , the case of more than 20% and within 30% as o, the case of more than 30% and within 50% as ⁇ , and the case of more than 50% as ⁇ .

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• Engineering & Computer Science (AREA)
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• Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

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• 2017
  • 2017-07-12 JP JP2017136374A patent/JP6291617B1/ja active Active
• 2018
  • 2018-07-12 CN CN201880046916.7A patent/CN110892108B/zh active Active
  • 2018-07-12 EP EP18832878.5A patent/EP3653784B1/fr active Active
  • 2018-07-12 WO PCT/JP2018/026302 patent/WO2019013277A1/fr not_active Ceased

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