CN111764173A - Treating agent for elastic fiber and elastic fiber - Google Patents
Treating agent for elastic fiber and elastic fiber Download PDFInfo
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- CN111764173A CN111764173A CN202010625846.XA CN202010625846A CN111764173A CN 111764173 A CN111764173 A CN 111764173A CN 202010625846 A CN202010625846 A CN 202010625846A CN 111764173 A CN111764173 A CN 111764173A
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- 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
- D06M15/643—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
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- 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
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- 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
- D06M13/322—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 nitrogen
- D06M13/46—Compounds containing quaternary nitrogen atoms
- D06M13/463—Compounds containing quaternary nitrogen atoms derived from monoamines
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- 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
- D06M2101/38—Polyurethanes
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- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Provided are a treating agent for elastic fibers which can improve stability, and elastic fibers to which the treating agent for elastic fibers is attached. The treating agent for elastic fiber of the present invention is characterized by containing: at least one base component selected from the group consisting of silicone oils, mineral oils, polyolefins, and ester oils; amine salts of alkyl phosphate esters; and at least one quaternary ammonium salt selected from quaternary ammonium salts of fatty acids, alkyl sulfonates, alkyl sulfates and alkyl phosphates. The elastic fiber of the present invention is characterized in that the above-mentioned treating agent for elastic fiber is adhered thereto.
Description
Technical Field
The present invention relates to a treatment agent for elastic fibers capable of improving stability, and elastic fibers to which the treatment agent for elastic fibers is attached.
Background
For example, elastic fibers such as polyurethane elastic fibers have stronger adhesion between fibers than other synthetic fibers such as polyester fibers and polyamide fibers. Therefore, for example, when an elastic fiber is spun and wound into a package, and then pulled out from the package and supplied to a processing step, there is a problem that it is difficult to stably unwind the elastic fiber from the package. Therefore, in order to improve the smoothness of elastic fibers compared to conventional elastic fibers, a treatment agent for elastic fibers containing a smoothing agent such as silicone oil is sometimes used.
Conventionally, there have been known treating agents for elastic fibers disclosed in International publication Nos. 2016-. International publication No. 2016-129357 discloses a treating agent for elastic fibers, which comprises a base component such as silicone oil and a specific alkyl phosphate. Japanese patent No. 6328836 discloses a treating agent for elastic fibers, which contains a smoothing agent (containing a paraffin component in an amount of 40% by mass or more and an aromatic component in an amount of 10% by mass or less) and a compound containing a sulfur element. Japanese patent laid-open publication No. 2009-138282 discloses a treating agent for elastic fibers, which contains 0.01 to 10 mass% of a base component such as silicone oil and a quaternary ammonium phosphate salt. Japanese patent application laid-open No. 2017-203222 discloses a treating agent for elastic fibers, which contains a smoothing agent, a Guerbet alcohol having 12 to 24 carbon atoms, and a charge control agent.
Disclosure of Invention
Problems to be solved by the invention
However, these proposals have a problem that the stability of the treating agent for elastic fibers containing a base component is not sufficient.
The present invention addresses the problem of providing a treatment agent for elastic fibers that can improve stability, and elastic fibers to which the treatment agent for elastic fibers has been attached.
Means for solving the problems
The present inventors have conducted studies to solve the above problems, and as a result, have found that a structure in which an amine salt of an alkyl phosphate and a predetermined quaternary ammonium salt are blended with a treating agent for elastic fibers containing a base component is preferable.
In order to solve the above problems, a treating agent for elastic fibers according to one embodiment of the present invention is characterized by containing at least one base component selected from the group consisting of silicone oil, mineral oil, polyolefin, and ester oil; amine salts of alkyl phosphate esters; and at least one quaternary ammonium salt selected from quaternary ammonium salts of fatty acids, alkyl sulfonates, alkyl sulfates and alkyl phosphates.
In the agent for treating elastic fibers, the amine salt of an alkyl phosphate is preferably at least one selected from the group consisting of a compound represented by the following chemical formula 1 and a compound represented by the following chemical formula 2.
(in the chemical formula (1),
A1o is an oxyalkylene group having 2 to 4 carbon atoms,
a is an integer of 0 to 30,
R1a residue obtained by removing a hydroxyl group from a branched alcohol having 8 to 32 carbon atoms,
m is an integer of 1 or 2,
R2、R3、R4a straight-chain alkyl group having 1 to 30 carbon atoms, a branched alkyl group having 3 to 30 carbon atoms, an alkenyl group having 2 to 30 carbon atoms, a hydroxyalkyl group having 1 to 30 carbon atoms, a polyoxyalkylene group having 1 to 30 carbon atoms, or a hydrogen atom,
wherein R is in the molecule1、(A1O)aWhen there are 2 or more, they may be the same or different from each other. )
(in the chemical formula (2),
A2o is an oxyalkylene group having 2 to 4 carbon atoms,
b is an integer of 0 to 30,
R5a residue obtained by removing a hydroxyl group from a branched alcohol having 8 to 32 carbon atoms,
n is an integer of 1 or 2,
Q1is hydroxy or R5O(A2O)b-，
R6、R7、R8Respectively a straight-chain alkyl group having 1 to 30 carbon atoms and a branched-chain alkyl group having 3 to 30 carbon atomsA group, an alkenyl group having 2 to 30 carbon atoms, a hydroxyalkyl group having 1 to 30 carbon atoms, a polyoxyalkylene group having 1 to 30 carbon atoms, or a hydrogen atom,
wherein R in the molecule5、(A2O)bWhen there are 2 or more, they may be the same or different from each other. )
In the treating agent for elastic fiber, the amine salt of alkyl phosphate is R selected from the group consisting of the salts of R in the formula (1)1A compound having a residue obtained by removing a hydroxyl group from a Guerbet alcohol and R in the chemical formula (2)5At least one compound which is a residue obtained by removing a hydroxyl group from a Guerbet alcohol.
In the treating agent for elastic fiber, it is preferable that the base component, the amine salt of alkyl phosphate ester and the quaternary ammonium salt are contained in a proportion of 80 to 99.98% by mass, the amine salt of alkyl phosphate ester is contained in a proportion of 0.01 to 10% by mass and the quaternary ammonium salt is contained in a proportion of 0.01 to 10% by mass, when the total content of the base component, the amine salt of alkyl phosphate ester and the quaternary ammonium salt is 100% by mass.
In order to solve the above problems, another aspect of the present invention provides an elastic fiber, wherein the elastic fiber treatment agent is adhered.
ADVANTAGEOUS EFFECTS OF INVENTION
According to the present invention, the stability of the treatment agent for elastic fibers can be improved.
Detailed Description
(embodiment 1)
Next, embodiment 1 of a treating agent for elastic fibers (hereinafter referred to as a treating agent) embodying the present invention will be described. The treating agent of the present embodiment contains a base component, an amine salt of an alkyl phosphate, and a predetermined quaternary ammonium salt.
Examples of the base component to be supplied to the treatment agent of the present embodiment include silicone oil, mineral oil, polyolefin, and ester oil. The base component may be used singly or 2 or more kinds may be suitably used in combination. The base component is blended as a smoothing agent in the treatment agent to impart smoothness to the elastic fiber.
Specific examples of the silicone oil are not particularly limited, and examples thereof include dimethyl silicone, phenyl-modified silicone, amino-modified silicone, amide-modified silicone, polyether-modified silicone, amino polyether-modified silicone, alkyl aralkyl-modified silicone, alkyl polyether-modified silicone, ester-modified silicone, epoxy-modified silicone, carbinol-modified silicone, mercapto-modified silicone, and polyoxyalkylene-modified silicone. These silicone oils may be suitably used as commercially available ones.
Examples of the mineral oil include aromatic hydrocarbons, paraffin hydrocarbons, and naphthene hydrocarbons. More specifically, for example, spindle oil, liquid paraffin, and the like can be given. Commercially available products can be suitably used as these mineral oils.
As polyolefins, poly-alpha-olefins used as smoothing agents are used. Specific examples of the polyolefin include poly- α -olefins obtained by polymerizing 1-butene, 1-hexene, 1-decene, and the like. The poly-alpha-olefin may be suitably used as a commercially available product.
Examples of the ester oil are not particularly limited, and ester oils produced from fatty acids and alcohols can be cited. Examples thereof include ester oils produced from fatty acids having an odd number or an even number of hydrocarbon groups and alcohols, as described later.
The fatty acid as a raw material of the ester oil is not particularly limited in the number of carbon atoms, the presence or absence of a branch, the number of elements, and the like, and may be, for example, a higher fatty acid, a fatty acid having a cyclic structure, or a fatty acid having an aromatic ring. The alcohol as a raw material of the ester oil is not particularly limited in the number of carbon atoms, the presence or absence of a branch, the number of elements, and the like, and may be, for example, a higher alcohol, an alcohol having a cyclic structure, or an alcohol having an aromatic ring.
Specific examples of ester oils include: (1) ester compounds of aliphatic monoalcohols and aliphatic monocarboxylic acids such as octyl palmitate, oleyl laurate, oleyl oleate, and isotetradecyl oleate; (2) ester compounds of aliphatic polyhydric alcohols and aliphatic monocarboxylic acids such as 1, 6-hexanediol dicaprate, glycerol trioleate, trimethylolpropane trilaurate and pentaerythritol tetracaprylate; (3) ester compounds of aliphatic monoalcohols and aliphatic polycarboxylic acids such as dioleyl azelate, dioleyl thiodipropionate, diisohexadecyl thiodipropionate and diisostearyl thiodipropionate; (4) ester compounds of aliphatic monocarboxylic acids and aromatic monoalcohols such as benzyl oleate and benzyl laurate; (5) a full ester compound of an aromatic polyhydric alcohol such as bisphenol a dilaurate and an aliphatic monocarboxylic acid; (6) full ester compounds of aliphatic monoalcohols such as bis (2-ethylhexyl) phthalate, diisostearyl isophthalate and trioctyl trimellitate with aromatic polycarboxylic acids; (7) natural oils such as coconut oil, rapeseed oil, sunflower seed oil, soybean oil, castor oil, sesame oil, fish oil, and beef tallow; and so on.
The alkyl group constituting the amine salt of the alkyl phosphate may be linear or branched. Among these, an alkyl group having a branch is preferable because the shape characteristics when the elastic fiber is wound are excellent. As the alkyl group having a branch, either an alkyl group branched at the α -position or an alkyl group branched at the β -position may be used. Among these, an alkyl group branched at the β -position is preferable for the purpose of providing the excellent effects of the present invention. The number of carbon atoms of the alkyl group is not particularly limited, but is preferably 1 to 32 carbon atoms, more preferably 8 to 32 carbon atoms. Specific examples of the alkyl group include a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, a hexyl group, a heptyl group, an octyl group, a decyl group, an undecyl group, a dodecyl group, a tridecyl group, a tetradecyl group, a pentadecyl group, a hexadecyl group, a heptadecyl group, an octadecyl group, an eicosyl group, an isopropyl group, an isobutyl group, an isopentyl group, an isohexyl group, an isoheptyl group, an isooctyl group, an isodecyl group, an isoundecyl group, an isododecyl group, an isotridecyl group, an isotetradecyl group, an isopentadecyl group, an isohexadecyl group, an isoheptadecyl group.
The alkyl phosphate ester may be an ester compound of a polyoxyalkylene alkyl ether (which is a 1-membered aliphatic alcohol and an alkylene oxide bonded via an ether bond) and phosphoric acid. Specific examples of the alkylene oxide to be supplied to the polyoxyalkylene alkyl ether include ethylene oxide, propylene oxide, butylene oxide, and the like. The number of moles of alkylene oxide added to 1 mole of alkyl group is preferably 1 to 50 moles, more preferably 1 to 30 moles, and still more preferably 1 to 10 moles.
The phosphoric acid may be orthophosphoric acid or polyphosphoric acid such as diphosphoric acid. The phosphoric acid is preferably orthophosphoric acid or diphosphoric acid in order to improve the stability of the treating agent.
Specific examples of the amine constituting the amine salt of the alkyl phosphate ester include: (1) aliphatic amines such as methylamine, dimethylamine, trimethylamine, ethylamine, diethylamine, triethylamine, N-diisopropylethylamine, butylamine, dibutylamine, 2-methylbutylamine, tributylamine, octylamine, and dimethyllaurylamine; (2) aromatic amines or heterocyclic amines such as aniline, N-methylbenzylamine, pyridine, morpholine, piperazine, and derivatives thereof; (3) alkanolamines such as monoethanolamine, N-methylethanolamine, diethanolamine, triethanolamine, isopropanolamine, diisopropanolamine, triisopropanolamine, dibutylethanolamine, butyldiethanolamine, octyldiethanolamine, and lauryldiethanolamine; (4) arylamines such as N-methylbenzylamine; (5) polyoxyalkylene alkyl amino ethers such as polyoxyethylene lauryl amino ether and polyoxyethylene stearyl amino ether; (6) ammonia; and so on.
The amine salt of the alkyl phosphate may be used alone or in combination of 2 or more kinds.
The amine salt of the alkyl phosphate is preferably at least one selected from the group consisting of a compound represented by the following chemical formula (1) and a compound represented by the following chemical formula (2). The effect of the present invention, particularly the shape characteristics when the elastic fiber to which the treating agent is added is wound into a package shape, can be improved by using the compound represented by the following chemical formula (1) or the compound represented by the following chemical formula (2).
(in the chemical formula (1),
A1o is an oxyalkylene group having 2 to 4 carbon atoms,
a is an integer of 0 to 30,
R1is a branched alcohol having 8 to 32 carbon atomsWherein the hydroxyl group is removed to obtain a residue,
m is an integer of 1 or 2,
R2、R3、R4a straight-chain alkyl group having 1 to 30 carbon atoms, a branched alkyl group having 3 to 30 carbon atoms, an alkenyl group having 2 to 30 carbon atoms, a hydroxyalkyl group having 1 to 30 carbon atoms, a polyoxyalkylene group having 1 to 30 carbon atoms, or a hydrogen atom,
wherein R is in the molecule1、(A1O)aWhen there are 2 or more, they may be the same or different from each other. )
(in the chemical formula (2),
A2o is an oxyalkylene group having 2 to 4 carbon atoms,
b is an integer of 0 to 30,
R5a residue obtained by removing a hydroxyl group from a branched alcohol having 8 to 32 carbon atoms,
n is an integer of 1 or 2,
Q1is hydroxy or R5O(A2O)b-，
R6、R7、R8A straight-chain alkyl group having 1 to 30 carbon atoms, a branched alkyl group having 3 to 30 carbon atoms, an alkenyl group having 2 to 30 carbon atoms, a hydroxyalkyl group having 1 to 30 carbon atoms, a polyoxyalkylene group having 1 to 30 carbon atoms, or a hydrogen atom,
wherein R in the molecule5、(A2O)bWhen there are 2 or more, they may be the same or different from each other. )
In addition, R is preferable in the above chemical formula (1)1A compound which is a residue obtained by removing a hydroxyl group from a Guerbet alcohol. In addition, R is preferable in the chemical formula (2)5A compound which is a residue obtained by removing a hydroxyl group from a Guerbet alcohol. The effect of the present invention can be further improved by using the compound.
Examples of the quaternary ammonium salt to be used in the treatment agent of the present embodiment include at least one selected from quaternary ammonium fatty acid salts, alkyl sulfonate salts, alkyl sulfate ester salts, and alkyl phosphate ester salts. The quaternary ammonium salts may be used singly or in combination of 2 or more kinds as appropriate.
Specific examples of quaternary ammonium constituting the quaternary ammonium salt include tetramethylammonium, triethylmethylammonium, tripropylethylammonium, tripropylmethylammonium, tributylmethylammonium, tetrabutylammonium, triisooctylethylammonium, trimethyloctylammonium, lauryl trimethylammonium, dilauryldimethylammonium, trimethylstearylammonium, dimethyldioleylammonium, dibutyldiethylammonium, triethyleicosenylammonium, trimethyloleylammonium, tributylhydroxyethylammonium, di (hydroxyethyl) dipropylammonium, (2-hydroxyethyl) dimethyloctylammonium, tri (hydroxyethyl) octylammonium, tri (hydroxypropyl) methylammonium, fatty acid dimethylaminopropylamide, fatty acid diethylaminoethylamide, and the like.
Specific examples of the fatty acid constituting the quaternary ammonium fatty acid salt include aliphatic carboxylic acids having 1 to 30 carbon atoms such as acetic acid, caproic acid, lauric acid, 2-ethylhexanoic acid, isostearic acid, oleic acid, erucic acid, malonic acid, adipic acid, sebacic acid, pentadecenylsuccinic acid, aliphatic hydroxycarboxylic acids having 3 to 30 carbon atoms such as lactic acid, ricinoleic acid, 12-hydroxystearic acid, and sulfur-containing aliphatic carboxylic acids having 3 to 30 carbon atoms such as thiodipropionic acid. Groups obtained by partially or completely removing hydrogen ions from these fatty acids are used as the anionic groups.
Specific examples of the alkylsulfonic acid constituting the quaternary ammonium alkylsulfonate include alkylsulfonic acids having 1 to 30 carbon atoms such as methanesulfonic acid, ethylsulfonic acid, butylsulfonic acid, laurylsulfonic acid, stearylsulfonic acid and oleylsulfonic acid. Groups obtained by partially or completely removing hydrogen ions from these alkylsulfonic acids are used as anionic groups.
Specific examples of the alkyl sulfate ester salt constituting the quaternary ammonium salt include alkyl sulfates having 1 to 30 carbon atoms such as methyl sulfate, ethyl sulfate and lauryl sulfate. Groups obtained by partially or completely removing hydrogen ions from these alkyl sulfates are used as anionic groups.
Specific examples of the alkyl phosphate constituting the quaternary ammonium alkyl phosphate salt include alkyl phosphates having 1 to 30 carbon atoms such as methyl phosphate, diethyl phosphate, dioctyl phosphate, and methyl oleyl phosphate. Groups obtained by partially or completely removing hydrogen ions from these alkyl phosphates are used as anionic groups.
The quaternary ammonium salts described above can be synthesized by a known method. Among them, for example: 1) a method of reacting the corresponding tertiary amine with a trialkyl phosphate; 2) a method of reacting the corresponding tertiary amine with a dialkyl sulfuric acid; 3) a method of reacting ethylene oxide with a corresponding tertiary amine in the presence of water to form a quaternary ammonium hydroxide, followed by reacting it with a sulfonic acid ester; 4) a method of reacting a corresponding tertiary amine with an alkyl halide to form a quaternary ammonium halide, followed by reacting it with a carboxylic acid metal salt; and so on.
The content ratio of the base component, the amine salt of the alkyl phosphate, and the quaternary ammonium salt in the treating agent of the present embodiment is not particularly limited. In the treatment agent of the present embodiment, it is preferable that the base component, the amine salt of the alkyl phosphate and the quaternary ammonium salt are contained in a proportion of 80 to 99.98% by mass, the amine salt of the alkyl phosphate is contained in a proportion of 0.01 to 10% by mass, and the quaternary ammonium salt is contained in a proportion of 0.01 to 10% by mass, when the total content of the base component, the amine salt of the alkyl phosphate and the quaternary ammonium salt is 100% by mass. By limiting to this range, the effects of the present invention, particularly antistatic properties, are further improved.
(embodiment 2)
Next, embodiment 2 of the elastic fiber embodying the present invention will be described. The elastic fiber of the present embodiment has the treating agent of embodiment 1 adhered thereto. The amount of the treating agent (not including a solvent) to be attached to the elastic fibers in embodiment 1 is not particularly limited, but is preferably 0.1 to 10 mass% in order to further improve the effect of the present invention.
Examples of the elastic fiber include, but are not particularly limited to, polyester elastic fiber, polyamide elastic fiber, polyolefin elastic fiber, and polyurethane elastic fiber. Among these, polyurethane elastic fibers are preferable. In this case, the expression of the effect of the present invention can be further improved.
The method for producing elastic fibers according to the present embodiment includes oiling the elastic fibers with the treatment agent according to embodiment 1. As a method of applying the treating agent, it is preferable to apply the treating agent to the elastic fiber by a net application method without dilution in a spinning step of the elastic fiber. As the adhesion method, for example, a known method such as a roll oil feeding method, an oil guide feeding method, and a spray oil feeding method can be applied. The oil feed roller is usually positioned between the head and the traverse winding device, and it can be applied to the manufacturing method of the present embodiment. Among these, the treatment agent of embodiment 1 is preferable because the effect can be remarkably exhibited when the treatment agent is attached to an elastic fiber, for example, a polyurethane elastic fiber, by an oil feed roller positioned between a stretching roller and a stretching roller.
The method for producing the elastic fiber itself used in the present embodiment is not particularly limited, and can be produced by a known method. Examples thereof include a wet spinning method, a melt spinning method, and a dry spinning method. Among these, the dry spinning method is preferably applied in view of excellent quality and production efficiency of the elastic fiber.
The action and effect of the treating agent and elastic fiber of the present embodiment will be described.
(1) The above embodiment is configured by blending an amine salt of an alkyl phosphate and a predetermined quaternary ammonium salt in a treating agent containing a base component. This can improve the stability, particularly the long-term stability, of the treatment agent without particularly deteriorating other characteristics.
Further, the shape characteristics of the elastic fiber to which the treatment agent is added, particularly the shape characteristics when wound in a cheese shape, can be improved. In addition, the antistatic property of the elastic fiber can be improved.
The above embodiment may be modified as follows.
The treatment agent of the present embodiment may further contain a component generally used in treatment agents such as a thickener, an antioxidant, and an ultraviolet absorber as a stabilizer or a charge control agent for maintaining the quality of the treatment agent, within a range not to impair the effects of the present invention.
Examples
Hereinafter, examples and the like are given to more specifically explain the constitution and effects of the present invention, but the present invention is not limited to these examples. In the following description of examples and comparative examples, parts means parts by mass, and% means% by mass.
Test group 1 (preparation of treating agent for elastic fiber)
The treating agents for elastic fibers used in the examples and comparative examples were prepared by the following preparation methods using the components shown in tables 1 to 3.
The amine salts (P-1-1a to P-5-1b) of the alkyl phosphoric acid esters (monomers) represented by the above chemical formula (1) are shown in Table 1. R in the chemical formula (1)1、A1、a、m、R2、R3、R4The kind or value of (B) is shown in "R" of Table 11"column" A1"column", "a" column "," m "column" and "R2"column", "R3"column", "R4In the column of "C".
The amine salts (P-1-2 to P-5-2) of the alkyl phosphoric acid esters (multimers) represented by the above chemical formula (2) are shown in Table 2. R in the chemical formula (2)5、A2、b、n、Q1、R6、R7、R8The kind or value of (B) is shown in "R" of Table 25"column" A2"column", "b" column "," n "column" and "Q1"column", "R6"column", "R7"column", "R8In the column of "C".
The treating agent of example 1 was prepared by thoroughly and uniformly mixing 0.8 part (%) of dimethyllauryl amine salt of monoisostearyl phosphate (P-1-1a) and 0.2 part (%) of dimethyllauryl amine salt of diisooctadecyl phosphate (P-1-1b), 49 parts (%) of polydimethylsiloxane (L-1) and 49 parts (%) of mineral oil (L-2), and 1 part (%) of quaternary salt of diethyl sulfate of dimethylaminopropyl isostearic acid amide (A-1) shown in Table 1.
The types of the base component, the amine salt of the alkyl phosphate ester, and the quaternary ammonium salt in the treating agent for elastic fibers, and the proportions of the components when the total content of the components is 100% are shown in the column of "base component", the column of "amine salt of alkyl phosphate ester", and the column of "quaternary ammonium salt" in table 3.
The treating agents of examples 2 to 26 and comparative examples 1 to 9 were prepared by mixing the base component, the amine salt of alkyl phosphate and the quaternary ammonium salt at the ratios shown in table 3 in the same manner as the treating agent of example 1.
[ Table 1]
[ Table 2]
[ Table 3]
In the context of Table 3, the following examples are,
l-1 represents a polydimethylsiloxane,
l-2 represents a mineral oil,
p-1-1a represents a dimethyllauryl amine salt of a monoisostearyl phosphate,
p-1-1b represents a dimethyllauryl amine salt of diisooctadecyl phosphate,
p-1-2 represents a dimethyl lauryl amine salt of isooctadecyl phosphate (polymer),
p-2-1a represents the dibutylethanolamine salt of monoisohexadecyl phosphate,
p-2-1b represents the dibutylethanolamine salt of diisohexadecyl phosphate,
p-2-2 represents dibutylethanolamine salt of isohexadecyl phosphate (polymer),
p-3-1a represents a 2-methylbutylamine neutralized product of a phosphoric acid ester which is an ethylene oxide (hereinafter abbreviated as EO)4mol adduct of mono-2-octanol,
p-3-1b represents a 2-methylbutylamine neutralized product of a phosphate of EO4mol adduct of di-2-octanol,
p-3-2 represents a 2-methylbutylamine neutralized product of a phosphate ester (polymer) of EO4mol adduct of 2-octanol,
p-4-1a represents a N, N-diisopropylethylamine neutralized product of a phosphate of EO4mol adduct of mono-2-octanol,
p-4-1b represents a N, N-diisopropylethylamine neutralized product of a phosphate of EO4mol adduct of di-2-octanol,
p-4-2 represents the N, N-diisopropylethylamine neutralized product of phosphate (polymer) of EO4mol adduct of 2-octanol,
p-5-1a represents the dibutylethanolamine neutralized product of monolauryl phosphate,
p-5-1b represents the dibutyl ethanolamine neutralized product of dilauryl phosphate,
p-5-2 represents a dibutylethanolamine neutralized product of lauryl phosphate (polymer),
p-6-1a represents a potassium salt of monoisohexadecyl phosphate,
p-6-1b represents a potassium salt of diisohexadecyl phosphate,
p-6-2 represents a potassium salt of isohexadecyl phosphate (polymer),
p-7 represents the dibutylethanolamine salt of dodecylbenzene sulphonic acid,
a-1 represents the diethyl sulfate quaternary salt of dimethylaminopropylamide isostearate,
a-2 represents a methanesulfonic acid salt of 2-hydroxyethyl-dimethyloctylammonium,
a-3 represents a diethyl phosphate of lauryl trimethylammonium,
a-4 represents the acetate salt of dimethyl lauryl amine.
Test group 2 (production of elastic fiber)
First, a solution (35%) of polyurethane, which is composed of tetramethylene ether glycol having a molecular weight of 2900, bis- (p-isocyanatophenyl) -methane and ethylenediamine, in N, N-dimethylacetamide was polymerized to prepare a polymer solution (a).
Next, as an antioxidant, a 2 to 1 (mass ratio) mixture of polyurethane, which is produced by the reaction of t-butyldiethanolamine with methylene-bis (4-cyclohexyl isocyanate), and a polycondensate, which is a polycondensate of p-cresol and divinylbenzene, was used to prepare an N, N-dimethylacetamide solution (35%) of the mixture as the other additive solution (B).
The solutions (a) and (B) were uniformly mixed in the proportions of 96% and 4%, respectively, to prepare a spinning dope.
Using the spinning dope thus obtained, a 44dtex/3fil multifilament polyurethane elastic fiber was spun by a known dry spinning method used for spandex. Then, the treatment agents shown in examples 1 to 26 and comparative examples 1 to 9 were applied to the filaments in a solvent-free (neet) state by roll oiling with an oiling roller located between the stretching roller and the stretching roller before winding. The elastic fiber subjected to the roll oiling in the above manner was wound on a cylindrical paper tube having a length of 58mm at a winding speed of 600 m/min by a winder using a surface driven winding method (surface drive) via a traverse guide capable of providing a winding width of 38mm, to obtain a package 500g of a dry-spun polyurethane elastic fiber. The amount of the treatment agent for elastic fibers deposited was adjusted so that the rotational speed of the oiling roller was adjusted to 5% of the total amount of the treatment agent. The antistatic property of the elastic fiber and the shape characteristics when the elastic fiber was wound into a package in a cheese shape were evaluated using the thus obtained dry-spun polyurethane elastic fiber package. The stability of the treatment agent was also evaluated. The evaluation method is as follows.
Evaluation of antistatic Properties
The resistance value of 10g of the polyurethane elastic fiber drawn from the package was measured using a resistance measuring instrument (model SM-5E manufactured by Toyo radio industries, Ltd.) under an atmosphere of 25 ℃ X40% RH, and the measured value was evaluated in accordance with the following criteria. The results are shown in the column "antistatic property" in table 3.
◎ preferably has a resistance value of less than 1.0 × 109Ω (no problem at all, stable operation).
○ good, resistance value of 1.0 × 109Omega is more than or equal to 1.0 × 1011Ω (slightly close to each other in the warping step, but the operation can be stably performed without any problem).
△ (slightly worse), the resistance value was 1.0 × 1011Omega is more than or equal to 1.0 × 1012Ω (there was approach in the warping step and attachment of fly in the circular knitting step, but there was no problem in workability).
× (bad) resistance value of 1.0 × 1012Omega or more (the approach in the warping step is serious, the adhesion of fly in the circular knitting step is also serious, and the operation cannot be performed).
Evaluation of stability of treatment agent
Using the treating agent for elastic fiber prepared in test group 1, the treatment agent was left standing at 25 ℃ for 3 months, and the stability was evaluated according to the following criteria. The results are shown in the column "stability of treating agent" in table 3.
Excellent: no precipitation and separation, and the same uniform state as immediately after the preparation.
O (good): a very slight clouding was produced, but the mixture was returned to a uniform state by stirring as it was immediately after the preparation.
X (bad): precipitation and separation occur, and the solution cannot be restored to a uniform state by stirring.
Evaluation of the shape of the cheese
For a package (400g package), the maximum value (Wmax) and the minimum width (Wmin) of the package width are measured, the swelling amount (bulk) is obtained from the difference (Wmax-Wmin), and the shape of the yarn package is evaluated according to the following criteria. The results are shown in the column "package shape" in table 3.
Excellent: the expansion amount is less than 4 mm.
O (good): the expansion amount is 4mm or more and less than 6 mm.
Δ (slightly worse): the expansion amount is more than 6mm and less than 8 mm.
X (bad): the swelling capacity is more than 8 mm.
From the evaluation results of the examples in table 3 with respect to the comparative examples, it is also understood that the treatment agent of the present invention can improve the stability of the treatment agent and improve the shape characteristics and antistatic properties of the elastic fiber.
Claims (5)
1. A treating agent for elastic fibers, characterized by comprising:
at least one base component selected from the group consisting of silicone oils, mineral oils, polyolefins, and ester oils;
amine salts of alkyl phosphate esters; and
at least one quaternary ammonium salt selected from quaternary ammonium fatty acid salts, alkyl sulfonic acid salts, alkyl sulfate ester salts, and alkyl phosphate ester salts.
2. The agent for treating elastic fibers according to claim 1, wherein the amine salt of an alkyl phosphate is at least one selected from the group consisting of a compound represented by the following chemical formula 1 and a compound represented by the following chemical formula 2,
chemical formula 1
In the chemical formula 1, the metal oxide is represented by,
A1o is an oxyalkylene group having 2 to 4 carbon atoms,
a is an integer of 0 to 30,
R1a residue obtained by removing a hydroxyl group from a branched alcohol having 8 to 32 carbon atoms,
m is an integer of 1 or 2,
R2、R3、R4a straight-chain alkyl group having 1 to 30 carbon atoms, a branched alkyl group having 3 to 30 carbon atoms, an alkenyl group having 2 to 30 carbon atoms, a hydroxyalkyl group having 1 to 30 carbon atoms, a polyoxyalkylene group having 1 to 30 carbon atoms, or a hydrogen atom,
wherein R is in the molecule1、(A1O)aWhen there are 2 or more, they may be the same or different from each other;
chemical formula 2
In the chemical formula 2, the first and second,
A2o is an oxyalkylene group having 2 to 4 carbon atoms,
b is an integer of 0 to 30,
R5a residue obtained by removing a hydroxyl group from a branched alcohol having 8 to 32 carbon atoms,
n is an integer of 1 or 2,
Q1is hydroxy or R5O(A2O)b-，
R6、R7、R8A straight-chain alkyl group having 1 to 30 carbon atoms, a branched alkyl group having 3 to 30 carbon atoms, an alkenyl group having 2 to 30 carbon atoms, a hydroxyalkyl group having 1 to 30 carbon atoms, a polyoxyalkylene group having 1 to 30 carbon atoms, or a hydrogen atom,
wherein R in the molecule5、(A2O)bWhen there are 2 or more, they may be the same or different from each other.
3. The agent for treating elastic fiber according to claim 2, wherein the amine salt of alkyl phosphoric acid ester is R selected from the group consisting of formula 11A compound having a residue obtained by removing a hydroxyl group from Guerbet alcohol and R in chemical formula 25At least one compound which is a residue obtained by removing a hydroxyl group from a Guerbet alcohol.
4. The agent for treating elastic fibers according to any one of claims 1 to 3, wherein the base component, the amine salt of the alkyl phosphate ester, and the quaternary ammonium salt are contained at a ratio of 80 to 99.98% by mass, the amine salt of the alkyl phosphate ester is contained at a ratio of 0.01 to 10% by mass, and the quaternary ammonium salt is contained at a ratio of 0.01 to 10% by mass, when the total content ratio of the base component, the amine salt of the alkyl phosphate ester, and the quaternary ammonium salt is 100% by mass.
5. An elastic fiber characterized by having the treating agent for elastic fiber according to any one of claims 1 to 4 attached thereto.
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| JP3501586B2 (en) * | 1995-05-31 | 2004-03-02 | 竹本油脂株式会社 | Processing method of polyurethane elastic fiber |
| JP2009138282A (en) * | 2007-12-03 | 2009-06-25 | Matsumoto Yushi Seiyaku Co Ltd | Treating agent for elastic fibers and elastic fibers |
| JP2009197338A (en) * | 2008-02-19 | 2009-09-03 | Sanyo Chem Ind Ltd | Oil agent for elastic fiber |
| JP6606061B2 (en) * | 2014-02-21 | 2019-11-13 | 松本油脂製薬株式会社 | Elastic fiber treatment agent and elastic fiber |
| WO2016129357A1 (en) * | 2015-02-10 | 2016-08-18 | 松本油脂製薬株式会社 | Treatment agent for elastic fibers and use of same |
| JP6713273B2 (en) * | 2015-12-18 | 2020-06-24 | 松本油脂製薬株式会社 | Treatment agent for elastic fiber and its use |
| JP6026038B1 (en) * | 2016-05-10 | 2016-11-16 | 竹本油脂株式会社 | Elastic fiber treatment agent, elastic fiber treatment method, and elastic fiber |
| JP6125739B1 (en) * | 2017-02-07 | 2017-05-10 | 竹本油脂株式会社 | Elastic fiber treatment agent and elastic fiber |
| JP6858609B2 (en) * | 2017-03-24 | 2021-04-14 | 松本油脂製薬株式会社 | Elastic fiber treatment agent and elastic fiber |
| JP6345846B1 (en) * | 2017-05-26 | 2018-06-20 | 竹本油脂株式会社 | Treatment agent for elastic fiber and method for producing elastic fiber |
| JP6542452B1 (en) * | 2018-09-20 | 2019-07-10 | 竹本油脂株式会社 | Processing agents for synthetic fibers and synthetic fibers |
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| CN1386150A (en) * | 2000-07-31 | 2002-12-18 | 三洋化成工业株式会社 | Lubricants for elastic fiber |
| CN1664228A (en) * | 2004-03-05 | 2005-09-07 | 三洋化成工业株式会社 | Filature oil for elastic fibre |
| CN105064042A (en) * | 2015-09-22 | 2015-11-18 | 浙江华峰氨纶股份有限公司 | Spinning oil for endowing polyurethane elastic fiber with unwinding property and preparation method of spinning oil |
| JP6328836B1 (en) * | 2017-09-15 | 2018-05-23 | 竹本油脂株式会社 | Elastic fiber treatment agent and elastic fiber |
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