JPWO2011105386A1 - Treatment agent for polyurethane elastic fiber and polyurethane elastic fiber - Google Patents

Abstract

The object of the present invention is to solve the above-mentioned problems of the prior art and to provide a polyurethane elastic fiber treating agent capable of providing stable and excellent anti-sticking property, uniform unwinding property, antistatic property, smoothness and productivity, and It is providing the polyurethane elastic fiber to which the processing agent was provided. The present invention contains at least one base component (A) selected from silicone oil, mineral oil and ester oil, and an acidic phosphate ester salt (B) of a divalent cation of a Group 2 element metal, The phosphoric acid ester salt (B) has an acidic hydroxyl group, and the molar ratio of the acidic hydroxyl group to the divalent cation of the group 2 element metal is 95/5 to 5/95, and the acidic phosphorus occupies the entire treating agent. It is a processing agent for polyurethane elastic fibers whose weight ratio of an acid ester salt (B) is 0.001 to 60 weight%.

Description

  The present invention relates to a treatment agent for polyurethane elastic fibers and polyurethane elastic fibers.

In the spinning process, the elastic fibers are wound into a cheese shape after applying a treatment agent to form a string. The elastic fiber is a fiber that is easily stuck because it has viscoelasticity. In particular, in the inner layer portion of the thread body, the sticking progresses with time due to the pressure applied during winding. Therefore, when using an elastic fiber thread body, unwinding is poor and thread breakage is caused.
When winding the yarn from the kite body and processing it into a beam or knitted fabric, if the degree of sticking is greatly different between the inner layer portion and the outer layer portion of the kite body as described above, that is, if the uniform unwinding property is inferior, The difference between the unwinding tension of the outer layer and the unwinding tension of the outer layer becomes large. As a result, the Beam shape defect and the knitted fabric quality are deteriorated.
The processing agent for elastic fibers uses a hydrophobic base component such as silicone oil, mineral oil, or ester oil. Therefore, the antistatic property is insufficient. If the antistatic property is insufficient, when the elastic fiber and the cotton yarn are knitted, the cotton is adsorbed by the elastic fiber due to static electricity and clogs the yarn suction port, and the yarn breakage occurs at the yarn suction port. As a result, there is a problem that must be frequently cleaned.
In the Beaming process, the yarns come close to each other due to static electricity, causing yarn breakage and a beam shape defect. Smoothness is required to stabilize operability in the processing process.

  Patent Document 1 proposes a method of using a treatment agent in which a higher fatty acid metal soap is dispersed in polydimethylsiloxane or mineral oil as a method for preventing sticking. However, with this treatment agent, the higher fatty acid metal soap aggregates with time, separates and settles, and becomes non-uniform. When such a non-uniform treatment agent is applied to the elastic yarn, the higher fatty acid metal soap adheres to the elastic yarn non-uniformly, so that uniform smoothness and anti-sticking properties cannot be obtained. Further, since the degree of sticking greatly differs between the inner layer portion and the outer layer portion of the kite thread body, yarn breakage may occur in post-processing, and the quality of the knitted fabric may be deteriorated. In addition, aggregates of higher fatty acid metal soaps become scum in the process, and regular cleaning is necessary. Furthermore, since this treatment agent has low friction between fibers, it often causes poor shape of the thread body, insufficient antistatic properties, and fluff adsorption may occur during post-processing. is there.

  As an antistatic agent, a method using an alkali metal salt of an alkyl phosphate as a treating agent (Patent Document 2), a method using an alkali metal salt of an alkyl phosphate and an alkyl phosphate amine salt as a treating agent (see Patent Document 3), an organic sulfonic acid A method using a compound or an organic sulfate compound as a treating agent (see Patent Document 4), a method using a sulfosuccinate as a treating agent (see Patent Document 5), and the like have been proposed. However, since these antistatic agents have a strong polarity, the treatment agent composed of a hydrophobic component is poorly soluble in the base component and adheres unevenly to the elastic yarn. For this reason, uniform antistatic properties may not be obtained, and the scum may fall off from the elastic yarn in post-processing. Further, it has an adverse effect on smoothness and anti-sticking properties, and may cause yarn breakage when post-processing the elastic yarn. In addition, since organic sulfonic acid and organic sulfuric acid are strong acids and alkali metals are strong bases, when the silk thread body is wet-heat treated, these strong acids and strong bases may be liberated and thread strength deterioration may occur.

Japanese Patent Publication No. 37-4586 Japanese Laid-Open Patent Publication No. 4-146276 Japanese Unexamined Patent Publication No. 9-49167 Japanese Patent Laid-Open No. 11-61651 Japanese Unexamined Patent Publication No. 10-298864

  The object of the present invention is to solve the above-mentioned problems of the prior art and to provide a treatment agent for polyurethane elastic fibers which can provide stable and excellent anti-sticking property, uniform unwinding property, antistatic property, smoothness and productivity, and It is providing the polyurethane elastic fiber to which the processing agent was provided.

  As a result of intensive investigations to solve the above-mentioned problems, the inventors of the present invention are processing agents for polyurethane elastic fibers containing a base component (A) and further containing a specific acidic phosphate ester salt (B). The present inventors have found that the present application problem can be solved. That is, the present invention contains at least one base component (A) selected from silicone oil, mineral oil and ester oil, and an acidic phosphate ester salt (B) of a divalent cation of a group 2 element metal, The acidic phosphate ester salt (B) has an acidic hydroxyl group, and the molar ratio of the acidic hydroxyl group to the divalent cation of the Group 2 element metal is 95/5 to 5/95, and occupies the entire treatment agent. It is a processing agent for polyurethane elastic fibers whose weight ratio of acidic phosphate ester salt (B) is 0.001 to 60 weight%.

The divalent cation of the Group 2 element metal is preferably at least one selected from Be ²⁺ , Mg ²⁺ , Ca ²⁺ , Sr ²⁺ and Ba ²⁺ .

  The acidic phosphate ester salt is at least selected from an acidic phosphate ester (C), a Group 2 element metal hydroxide, a Group 2 element metal hydroxide, a Group 2 element metal oxide, and a Group 2 element metal carbonate. It is a product obtained by reacting one kind of component (D), and the molar ratio of the acidic hydroxyl group of the acidic phosphate ester (C) to the component (D) is 100/5 to 100/95. preferable.

（式（１）中のＲ^１は、炭素数が１〜３０の炭化水素基を示す。Ｘは炭素数２〜４のアルキレン基を表し、ＸＯとしてオキシアルキレン基を示す。ａはオキシアルキレン基の付加モル数を示し、０または１〜１５の整数である。ｂとｃは、各々、１又は２であり、ｂ＋ｃ＝３を満足する整数である。） The acidic phosphate ester (C) is preferably a compound represented by the following general formula (1).

(R ¹ in Formula (1) represents a hydrocarbon group having 1 to 30 carbon atoms. X represents an alkylene group having 2 to 4 carbon atoms, and XO represents an oxyalkylene group. A represents an oxyalkylene group. And is an integer of 0 or 1 to 15. b and c are each 1 or 2, and are integers satisfying b + c = 3.)

Furthermore, the present inventors also solved the present application problem in a treatment agent for polyurethane elastic fiber, which is obtained by blending acidic phosphate ester (C) and component (D) at a specific ratio with base component (A). I also found that I can do it. That is, the present invention relates to at least one base component (A) selected from silicone oil, mineral oil and ester oil, acidic phosphate ester (C), Group 2 element metal, Group 2 element metal hydroxide. At least one component (D) selected from a Group 2 element metal oxide and a Group 2 element metal carbonate is blended, and the acidic hydroxyl group of the acidic phosphate ester (C) and the component (D) ) Is 100/5 to 100/95, and the total weight ratio of the acidic phosphate ester (C) and the component (D) in the entire treatment agent is 0.001 to 60% by weight. And a processing agent for polyurethane elastic fiber.
The Group 2 element metal is preferably at least one selected from Be, Mg, Ca, Sr and Ba. The acidic phosphate ester (C) is preferably a compound represented by the general formula (1).

  The treating agent of the present invention is selected from alkyl-modified silicones, ester-modified silicones, polyether-modified silicones, carbinol-modified silicones, carboxy-modified silicones, amino-modified silicones, amino-modified silicone neutralized organic phosphate esters, and silicone resins. It is preferable that the composition further contains at least one component, and the weight ratio of the component to the entire treatment agent is 0.01 to 10% by weight.

  The polyurethane elastic fiber of the present invention is one in which the above-mentioned treating agent is added to the polyurethane elastic fiber main body in an amount of 0.1 to 15% by weight.

  The treatment agent for polyurethane elastic fiber of the present invention can impart stable and excellent anti-sticking property, uniform unwinding property, antistatic property, smoothness and productivity to polyurethane elastic fiber. Since the polyurethane elastic fiber of the present invention is provided with the treatment agent of the present invention, it has stable and excellent anti-sticking property, uniform unwinding property, antistatic property, smoothness and productivity.

The schematic diagram explaining the measuring method of roller static electricity generation amount. The schematic diagram explaining the measuring method of knitting tension | tensile_strength, and the measuring method of the amount of static electricity generation. The schematic diagram explaining the measuring method of the friction coefficient between fibers. The schematic diagram explaining the measuring method of an unwinding speed ratio and a scum. The schematic diagram explaining the measuring method of thread | yarn strength.

  The treatment agent for polyurethane elastic fibers of the present invention (hereinafter sometimes referred to as treatment agent) contains a base component (A) and further contains a specific acidic phosphate ester salt (B). Moreover, the processing agent of this invention is also a processing agent formed by mix | blending a base component (A), acidic phosphate ester (C), and a component (D). Details will be described below.

[Base component (A)]
The base component (A) of the present invention is at least one selected from silicone oil, mineral oil and ester oil. Therefore, you may use together 1 type, or 2 or more types as a base component.

The silicone oil is not particularly limited, and examples thereof include polydimethylsiloxane, polyalkylsiloxane, and polyalkylphenylsiloxane. You may use together 1 type, or 2 or more types.
The number average molecular weight of the silicone oil is preferably 700 or more, more preferably 800 to 4000, and still more preferably 1000 to 3000. The viscosity of the silicone oil (25 ° C.) is preferably from 5 to 50 mm ² / s, more preferably 6~40mm ² / s, more preferably 9~30mm ² / s.

Siloxane bonds of the silicone oil ^{(SiOR 2 R 3: R 2} , R 3 are each independently an organic group) coupling amount is preferably 10 to 55, more preferably from 12 to 45, is 14 to 40 Further preferred. The organic groups of R ² and R ³ are hydrocarbon groups having 1 to 24 carbon atoms, and are methyl group, ethyl group, propyl group, isopropyl group, butyl group, isobutyl group, pentyl group, isopentyl group, hexyl group, cyclohexane A propyl group, a cyclohexyl group, a phenyl group, a benzyl group and the like can be mentioned, and a methyl group and a phenyl group are particularly preferable.
The proportion of silicone oil in the total base component is preferably 40% by weight or more, more preferably 50% by weight or more, and still more preferably 60% by weight or more. If it is less than 40% by weight, the smoothness of the yarn may be insufficient.

The mineral oil is not particularly limited, and examples thereof include machine oil, spindle oil, and liquid paraffin. Among these, as the mineral oil, liquid paraffin is preferable because the generation of odor is low. Mineral oil may use together 1 type, or 2 or more types.
The viscosity of mineral oil (25 ° C.) is preferably at least ^{5 mm} 2 / s, more preferably 5 to 50 mm ² / s, more preferably 5 to 30 mm ² / s. If the viscosity (25 ° C.) is less than 5 mm ² / s, the yarn may swell, which is not preferable.

  The proportion of the mineral oil in the entire base component is not particularly limited, but is preferably 40% by weight or more, more preferably 50% by weight or more, and further preferably 60% by weight or more. When the mineral oil is less than 40% by weight, the compatibility with the acidic phosphate ester salt (B) may be deteriorated.

  Although it does not specifically limit as ester oil, The ester manufactured from a fatty acid and alcohol can be mentioned. Examples of ester oils include esters produced from fatty acids selected from the following and alcohols, but esters that do not use the following fatty acids or alcohols as raw materials may also be used. The ester oil may be used alone or in combination of two or more.

  The fatty acid is not particularly limited in terms of its carbon number, presence or absence of branching, valence, etc., and may be a higher fatty acid, a cyclic fatty acid, or a fatty acid containing an aromatic ring. Examples of the fatty acid include caprylic acid, 2-ethylhexylic acid, capric acid, lauric acid, myristic acid, palmitic acid, stearic acid, isostearic acid, oleic acid, arachidic acid, behenic acid, lignoselenic acid, adipic acid, and sebacic acid. And benzoic acid. The alcohol is not particularly limited with respect to its carbon number, presence or absence of branching, valence, etc., and may be a higher alcohol, a cyclic alcohol, or an alcohol containing an aromatic ring. Examples of the alcohol include octyl alcohol, 2-ethylhexyl alcohol, decyl alcohol, lauryl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol, isostearyl alcohol, oleyl alcohol, ethylene glycol, hexanediol, glycerin, trimethylolpropane, Examples include pentaerythritol, sorbitol, sorbitan and the like.

The viscosity of the ester oil (25 ° C.) is preferably at least ^{5 mm} 2 / s, more preferably 5 to 50 mm ² / s, more preferably 5 to 30 mm ² / s. If the viscosity (25 ° C.) is less than 5 mm ² / s, the yarn may swell, which is not preferable.
The proportion of the ester oil in the entire base component is not particularly limited, but is preferably 50% by weight or less, more preferably 40% by weight or less, and further preferably 30% by weight or less. If the ester oil exceeds 50% by weight, the smoothness of the yarn may be insufficient.

[Acid phosphate ester salt (B)]
The processing agent for polyurethane elastic fibers of the present invention essentially contains an acidic phosphate ester salt (B) of a divalent cation of a Group 2 element metal. The acidic phosphate ester salt (B) may be one type or a mixture of two or more types.

  The acidic phosphate ester salt (B) of the present invention has an acidic hydroxyl group. That is, the acidic phosphate ester salt (B) has an acidic hydroxyl group in which the hydrogen atom of the acidic hydroxyl group is substituted with a divalent cation of a group 2 element metal and is not substituted with a divalent cation of a group 2 element metal It is what has. By having a group in which the hydrogen atom of the acidic hydroxyl group is substituted with a divalent cation, it exhibits excellent unwinding and antistatic properties. At the same time, by having a predetermined ratio of unsubstituted acidic hydroxyl groups, it is excellent in solubility in the base component, the unraveling property and antistatic property are stable and uniform, and there are few scums that fall off in post-processing. It is thought to show the characteristics.

Molar ratio of acidic hydroxyl group and divalent cation of group 2 element metal contained in acidic phosphate ester salt (B) (number of moles of acidic hydroxyl group (H) / number of moles of divalent cation of group 2 element metal (I) ) Is preferably 95/5 to 5/95, more preferably 90/10 to 30/70, still more preferably 85/15 to 40/60, and particularly preferably 80/20 to 50/50. When the molar ratio (H / I) exceeds 95/5, the effects of anti-sticking, uniform unwinding and antistatic properties may be insufficient, and the yarn strength may deteriorate. If the molar ratio (H / I) is less than 5/95, the compatibility with the base component will be insufficient, resulting in post-processing scum, inability to obtain uniform unraveling properties, and insufficient smoothness. There are things to do.
When unneutralized (H / I is 100/0), that is, when an acidic phosphate ester that does not constitute a salt is used, the yarn strength is more likely to deteriorate. Moreover, thread swelling may cause thread breakage during post-processing, or smoothness may be insufficient. In addition, the effects of anti-sticking, antistatic, and smoothness may be insufficient. On the other hand, in the case of complete neutralization (H / I is 0/100), that is, when a phosphate ester salt that does not have an acidic hydroxyl group is used, the compatibility with the base component is insufficient, so that scum is produced by post-processing. It tends to occur or the unraveling property becomes uneven. In addition, the anti-sticking and antistatic effects may not be fully exhibited. In addition, the friction against metal is high and the smoothness may be insufficient.

The divalent cation of the Group 2 element metal contained in the acidic phosphate ester salt (B) of the present invention is preferably at least one selected from Be ²⁺ , Mg ²⁺ , Ca ²⁺ , Sr ²⁺ and Ba ²⁺ . From the viewpoint of safety to the human body, Mg ²⁺ , Ca ²⁺ and Sr ²⁺ are more preferable.
In addition, when the acidic phosphate ester salt is a salt composed of a monovalent cation such as Na ⁺ , K ⁺ , NH ₄ ⁺ , the compatibility with the base component is higher than that of the acidic phosphate ester salt (B) of the present invention. Since it is low and insufficient, scum is likely to occur in post-processing. Moreover, these salts are inferior in the effect of unraveling property, smoothness, and antistatic property compared with the acidic phosphate ester salt (B) of the present invention.

  The acidic phosphate ester salt (B) of the present invention comprises an acidic phosphate ester (C), a Group 2 element metal hydroxide, a Group 2 element metal hydroxide, a Group 2 element metal oxide, and a Group 2 element metal carbonate. It is a product obtained by reacting at least one component (D) selected from salts. In this case, the molar ratio of the acidic hydroxyl group of the acidic phosphate ester (C) to the component (D) (the number of moles of the acidic hydroxyl group of the acidic phosphate ester (C) / the number of moles of the component (D)) was 100 / 5-100 / 95 are preferable, 100 / 10-100 / 70 are more preferable, 100 / 15-100 / 60 are still more preferable, and 100 / 20-100 / 50 are especially preferable. When the molar ratio exceeds 100/5, the effects of anti-sticking, uniform unwinding and antistatic properties may be insufficient, and the yarn strength may be deteriorated. If the molar ratio is less than 100/95, the compatibility with the base component may be insufficient, resulting in scum in post-processing, a uniform disentanglement may not be obtained, and smoothness may be insufficient. .

  As acidic phosphate ester (C), the compound represented by the said General formula (1) is preferable.
  In the general formula (1), R¹Is a hydrocarbon group having 1 to 30 carbon atoms. R ¹If the number of carbon atoms exceeds 30, the solubility of the acidic phosphate ester salt (B) produced using the acidic phosphate ester (C) in the base component is insufficient. R¹4-22 are preferable, 6-20 are more preferable, and 8-18 are especially preferable. Examples of the hydrocarbon group include a saturated or unsaturated aliphatic hydrocarbon group which may have a branch, an aromatic hydrocarbon group which may have a substituent, or a cyclic aliphatic hydrocarbon group. . From the viewpoint of solubility of the acidic phosphate ester salt (B) produced using the acidic phosphate ester (C) in the base component, R¹Is more preferably a branched hydrocarbon group than a linear hydrocarbon group. More preferably, it is a branched hydrocarbon group having 4 to 22 carbon atoms.
  The oxyalkylene group XO is preferably oxyethylene, oxypropylene, or oxybutylene, and preferably has 1 to 15 of these in the molecule. When the number of oxyalkylene groups XO in the molecule exceeds 15, the solubility of the acidic phosphate ester salt (B) produced using the acidic phosphate ester (C) in the base component is insufficient. More preferably, the number of oxyalkylene groups in the molecule is 1 to 5.

  The acidic phosphoric acid ester (C) represented by the above general formula (1) is a combination of b and c in the formula, and the acidic phosphoric acid monoester (C-1) represented by the following general formula (2) and the following: It can be distinguished from the acidic phosphoric acid diester (C-2) represented by the general formula (3).

（式（２）中のＲ^１、Ｘ、ＸＯ、ａは式（１）の場合と同じ）

(R ¹ , X, XO, and a in formula (2) are the same as in formula (1))

（式（３）中のＲ^１、Ｘ、ＸＯ、ａは式（１）の場合と同じ）

(R ¹ , X, XO, and a in formula (3) are the same as in formula (1))

  Specific examples of the acidic phosphate ester (C) include monomethyl phosphate ester, dimethyl phosphate ester, trimethyl phosphate ester, butyl phosphate ester, hexyl phosphate ester, octyl phosphate ester, decyl phosphate ester, lauryl phosphate ester, Myristyl phosphate, cetyl phosphate, stearyl phosphate, behenyl phosphate, trioctacosanyl phosphate, oleyl phosphate, 2-ethylhexyl phosphate, isoheptyl phosphate, isooctyl phosphate, isononyl phosphate Acid ester, isodecyl phosphate, isoundecyl phosphate, isolauryl phosphate, isotridecyl phosphate, isomyristyl phosphate, isocetyl phosphate Steal, isostearyl phosphate, t-butyl phosphate, benzyl phosphate, octylphenyl phosphate, cyclohexyl phosphate, polyoxyethylene 5 mol addition cetyl ether phosphate, polyoxyethylene 15 mol addition cetyl ether Phosphate ester, polyoxyethylene 7 mol addition polyoxypropylene 3.5 mol addition secondary alkyl ether phosphate ester, polyoxyethylene 2 mol polyoxypropylene 5 mol phosphate ester, polyoxyethylene 3 mol addition secondary alkyl ether phosphate ester And polyoxyethylene 2-mole addition lauryl ether phosphate, polyoxyethylene 4-mole addition phenol phosphate, and the like.

The acidic phosphate ester (C) can be synthesized by a known method. For example, it can be obtained by reacting an inorganic phosphoric acid such as P ₂ O ₅ with a compound having an alcoholic hydroxyl group in the molecule such as alcohol or polyoxyalkylene-added alkyl ether in an arbitrary molar ratio.
The molar ratio of _P 2 _{O 5} with respect to 1 mol of the compound such as alcohol is preferably from 0.4 to 0.15. 0.335 to 0.2 is more preferable, and 0.3 to 0.25 is particularly preferable. If it exceeds 0.4, the solubility of the acidic phosphate ester salt (B) produced using the acidic phosphate ester (C) in the base component may be insufficient, or the smoothness may be lowered. If it is less than 0.15, the unwinding performance and antistatic performance may deteriorate.

When inorganic phosphoric acid such as P ₂ O ₅ is reacted with alcohol, a mixture of acidic phosphoric acid monoester (C-1) and acidic phosphoric acid diester (C-2) can be obtained. In that case, the ratio of the acidic phosphoric acid monoester (C-1) and acidic phosphoric diester (C-2) obtained can be adjusted by adjusting the molar ratio of P ₂ O ₅ to 1 mol of alcohol. . As acidic phosphoric acid ester (C) used for manufacture of acidic phosphoric acid ester salt (B) of this invention, acidic phosphoric acid monoester (C-1) and acidic phosphoric acid diester (C-2) are respectively independent. Although a mixture may be sufficient, a mixture is preferable. The molar ratio (C-1 / C-2) of the acidic phosphoric acid monoester (C-1) to the acidic phosphoric acid diester (C-2) is preferably 5/95 to 80/20, and 10/90 to 70/30. Is more preferable, and 15/85 to 50/50 is more preferable from the viewpoint of antistatic property, unraveling property, and solubility in the base component of the acidic phosphate ester salt (B) obtained by the reaction.

  The molar ratio of (C-1) and (C-2) in the mixture of acidic phosphoric acid monoester (C-1) and acidic phosphoric acid diester (C-2) can be confirmed by a known potentiometric titration method.

  The following can be mentioned as a component (D). As a hydroxide of a Group 2 element metal, Be (OH)₂, Mg (OH)₂, Ca (OH)₂, Sr (OH)₂, Ba (OH)₂Is preferred, Mg (OH)₂, Ca (OH)₂, Sr (OH)₂Is more preferable. As the Group 2 element metal oxide, BeO, MgO, CaO, SrO, and BaO are preferable, and MgO, CaO, and SrO are more preferable. As the carbonate of group 2 element metal, BeCO₃, MgCO₃, CaCO₃, SrCO₃, BaCO₃Is preferred, MgCO₃, CaCO₃, SrCO ₃Is more preferable. As the group 2 element metal, Be, Mg, Ca, Sr, and Ba are preferable, and Mg, Ca, and Sr are more preferable.

  The production method of the acidic phosphate ester salt (B) is not particularly limited, but the acidic hydroxyl group of the acidic phosphate ester (C) is a hydroxide of a group 2 element metal, an oxide of a group 2 element metal, or a group 2 element. The method of preparing by neutralizing using a metal carbonate etc., and the method of preparing by reacting acidic phosphate ester (C) and a group 2 element metal directly are preferable. In addition, as will be described later with the processing agent, the base component (A), the acidic phosphate ester (C) and the component (D) are directly blended in the above-mentioned ratio, mixed and stirred, and reacted in the processing agent. You may make it contain acidic phosphate ester salt (B).

  When the acidic hydroxyl group of the acidic phosphate ester (C) is neutralized with a hydroxide of a group 2 element metal, an oxide of a group 2 element metal, a carbonate of a group 2 element metal, or the like, When directly reacting C) with the Group 2 element metal, it is preferable to dilute these substrates in a solvent as necessary. As the solvent, those having good compatibility with the base component are preferable, and examples thereof include mineral oil, alcohol, nonionic activator, ester oil and the like. As the mineral oil, liquid paraffin is preferable. As alcohol, octyl alcohol, 2-ethylhexyl alcohol, decyl alcohol, lauryl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol, isostearyl alcohol, oleyl alcohol, ethylene glycol, hexanediol, glycerin, trimethylolpropane, pentaerythritol Sorbitol, sorbitan and the like. The nonionic activator is not particularly limited, and examples thereof include polyoxyalkylene-added secondary alkyl ether, polyoxyalkylene-added alkyl ether, polyoxyalkylene-added sorbitan ester, and the like. Although it does not specifically limit as ester oil, The ester manufactured from a fatty acid and alcohol can be mentioned.

  In the case of the above reaction, it is preferable to mix water in order to promote the reaction. The amount of water mixed during the reaction is not particularly limited, but if water remains in the reaction product, the compatibility with the base component of the treatment agent may deteriorate. Therefore, it is desirable that the amount is as small as 0.1 to 5% with respect to the total amount of the substrate. It is more preferable to remove residual water in the reaction product by a treatment such as heating after the reaction. From the same point of view, water generated when the acidic hydroxyl group of the acidic phosphate ester (C) is neutralized with a Group 2 element metal hydroxide, a Group 2 element metal oxide, a Group 2 element metal carbonate, or the like. Also, it is preferable to dehydrate by heating or the like. In addition, it is desirable that the amount of water in the treatment agent is small, preferably 5% or less, more preferably 1% or less, and still more preferably 0.1% or less.

The molar ratio (H) / (I) between the acidic hydroxyl group contained in the acidic phosphate ester salt (B) of the present invention and the divalent cation of the Group 2 element metal is the value of the acidic phosphate ester (C) before the reaction. From the acid value (F) and the acid value (G) of the acidic phosphoric ester salt (B) obtained by the reaction, it can be calculated by the mathematical formula (1).
(H) / (I) = (G) / [(F)-(G)] Formula (1)

[Reactive group value of component (D)]
The reactive valence (L) of at least one component (D) selected from Group 2 element metal hydroxides, Group 2 element metal hydroxides, Group 2 element metal oxides, and Group 2 element metal carbonates is: It can be calculated by Equation (2) using the formula amount (K) of (D).
(L) = [56100 / (K)] × 2 Formula (2)

[Calculation of molar ratio of acidic hydroxyl group of acidic phosphate ester (C) to component (D)]
When the molar ratio of the acidic hydroxyl group of the acidic phosphate ester (C) to the component (D) is 100 / (P), (P) is the reactive group value (L) of the component (D), component (D) % (N), the acid value (F) of the acidic phosphate ester (C), and the formula (3) using the weight percent (O) of the acidic phosphate ester (C).
(P) = [(L) × (N)] ÷ [(F) × (O)] × 100 Formula (3)

[Other ingredients]
The treatment agent of the present invention may further contain a modified silicone in order to improve antistatic properties and unwinding properties. The modified silicone is generally a reactive (functional) group or a non-reactive group at least at one of both ends, one end, side chain, and both side chains of polysiloxane such as dimethyl silicone (polydimethylsiloxane) ( It has a structure in which at least one functional group is bonded.

  Examples of the modified silicone include alkyl-modified silicones such as modified silicones having a long-chain alkyl group (such as an alkyl group having 6 or more carbon atoms or 2-phenylpropyl group); ester-modified silicones that are modified silicones having ester bonds; Polyether-modified silicones such as modified silicones having oxyalkylene groups (for example, polyoxyethylene groups, polyoxypropylene groups, polyoxyethyleneoxypropylene groups, etc.); carbinol-modified silicones having modified alcoholic hydroxyl groups; acids Carboxy-modified silicone which is a modified silicone having an anhydride group or carboxyl group; Amino-modified silicone which is a modified silicone having an amino group; The amino group of the amino-modified silicone is neutralized with an organic phosphate ester Amino organic phosphoric acid ester neutralization product of modified silicones and the like.

Further, the treatment agent of the present invention may further contain a silicone resin in order to improve antistatic properties and unwinding properties. The silicone resin means a silicone having a three-dimensional crosslinked structure, and may further contain other modified silicones and the like. The silicone resin is generally at least one component selected from a monofunctional constituent unit (M), a bifunctional constituent unit (D), a trifunctional constituent unit (T), and a tetrafunctional constituent unit (Q). It consists of units.
Examples of the silicone resin include silicone resins such as MQ silicone resin, MQT silicone resin, T silicone resin, and DT silicone resin.

As the MQ silicone resin, for example, R ^a R ^b R ^c SiO _1/2 that is ^a monofunctional structural unit (provided that R ^a, R ^b, and R ^c are all hydrocarbon groups) and tetrafunctional. And a silicone resin containing SiO _4/2 which is a structural unit.
Examples of the MQT silicone resin include R ^a R ^b R ^c SiO _1/2 that is ^a monofunctional structural unit (provided that R ^a , R ^b, and R ^c are all hydrocarbon groups) and a tetrafunctional group. And a silicone resin containing SiO _4/2 which is a structural unit and RSiO _3/2 which is a trifunctional structural unit (wherein R is a hydrocarbon group).
Examples of the T-silicone resin include a silicone resin containing RSiO _3/2 (where R is a hydrocarbon group) which is a trifunctional structural unit (the terminal of which is a hydrocarbon group, silanol group or alkoxy group). Or the like)).
The DT silicone resin, for example, a difunctional structural unit ^R a ^R b _{SiO 2/2} (where, any ^{R a,} and ^{R b} is a hydrocarbon group.) And, in trifunctional structural unit There can be mentioned RSiO _3/2 (where R is a hydrocarbon group).
The hydrocarbon group for R, R ^a , R ^b and R ^{c is} a hydrocarbon group having 1 to 24 carbon atoms, such as methyl group, ethyl group, propyl group, isopropyl group, butyl group, isobutyl group, pentyl group, An isopentyl group, a hexyl group, a cyclopropyl group, a cyclohexyl group, a phenyl group, a benzyl group and the like can be mentioned, and a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, and a phenyl group are particularly preferable.

  These modified silicones and silicone resins can be suitably used because they do not inhibit the compatibility between the acidic phosphate ester and the base component.

The treatment agent of the present invention can further contain components usually used for treatment agents for elastic fibers such as a binder, an antistatic agent, an antioxidant, and an ultraviolet absorber.
Examples of the binder include nonylphenol, oxyethylene adduct of nonylphenol, oxypropylene adduct of nonylphenol, dioctyl phthalate, isostearyl alcohol, oxyethylene adduct of isostearyl alcohol, oxypropylene adduct of isostearyl alcohol, isostearic acid Examples include acids, oleic acid, palmitic acid, stearic acid and the like. Examples of the antistatic agent include alkane sulfonate, dodecyl benzene sulfonate, alkyl phosphate ester amine salt, alkyl phosphate monovalent metal salt, and the like.

[Treatment agent for polyurethane elastic fiber]
The weight ratio of the base component (A) in the entire treatment agent of the present invention is preferably 40 to 99.999% by weight, more preferably 50 to 99.99% by weight, still more preferably 70 to 99.9% by weight, 90 to 99% by weight is particularly preferred. When the amount is less than 40% by weight, the solubility of the acidic phosphate ester salt (B) in the base component (A) is lowered, and the acid phosphate ester salt (B) does not uniformly adhere to the elastic yarn, and falls off during post-processing, resulting in scum. In addition, smoothness may be reduced.

  The weight proportion of the acidic phosphate ester salt (B) in the entire treatment agent of the present invention is 0.001 to 60% by weight, preferably 0.01 to 50% by weight, more preferably 0.1 to 30% by weight. Preferably, 1 to 10% by weight is more preferable. If it exceeds 60% by weight, the solubility in the base component is lowered, it does not uniformly adhere to the elastic yarn, it may fall off in post-processing, and scum may be produced, or the smoothness may be lowered.

  When the treatment agent of the present invention contains a modified silicone, the polymerization rate of the modified silicone in the entire treatment agent is not particularly limited, but is preferably 0.01 to 10% by weight, more preferably 0.05 to 7% by weight. 0.1 to 5% by weight is particularly preferable. If the weight ratio of the modified silicone is less than 0.01% by weight, the effect due to the addition may not be observed because the amount is too small. On the other hand, if it exceeds 10% by weight, the proper performance of the treatment agent may not be obtained.

  When the treatment agent of the present invention contains a silicone resin, the weight ratio of the silicone resin in the entire treatment agent is not particularly limited, but is preferably 0.01 to 10% by weight, more preferably 0.05 to 7% by weight. 0.1 to 5% by weight is particularly preferable. If the weight ratio of the silicone resin is less than 0.01% by weight, the effect of addition may not be seen. On the other hand, if it exceeds 10% by weight, an appropriate balance of treatment agent performance may not be maintained.

Although there is no limitation in particular about the manufacturing method of a processing agent, a base component (A) and acidic phosphate ester salt (B) can be mix | blended in a predetermined ratio, and it can stir and prepare.
Further, as described above, the base component (A), the phosphate ester (C) and the component (D), which are the raw materials of the acidic phosphate ester salt (B), are blended at a predetermined ratio, and mixed and stirred. A treating agent containing an acidic phosphate ester salt (B) may be prepared. In this case, the present invention can be expressed as a treatment agent comprising the aforementioned base component (A), acidic phosphate ester (C) and component (D). That is, the present invention comprises a base component (A), an acidic phosphate ester (C), and a component (D), wherein the acidic hydroxyl group of the acidic phosphate ester (C) and the component (D) The polyurethane has a molar ratio of 100/5 to 100/95, and the total weight ratio of the acidic phosphate ester (C) and the component (D) in the entire treating agent is 0.001 to 60% by weight. It can be expressed as a treatment agent for elastic fibers.

The molar ratio of the acidic hydroxyl group of the acidic phosphate ester (C) to the component (D) is the same as that described for the acidic phosphate ester salt (B).
The total weight ratio of the acidic phosphate ester (C) and the component (D) in the entire treatment agent is 0.001 to 60% by weight, preferably 0.01 to 50% by weight, and 0.1 to 30% by weight. % Is more preferable, and 1 to 10% by weight is more preferable. If it exceeds 60% by weight, the solubility in the base component is lowered, it does not uniformly adhere to the elastic yarn, it may fall off in post-processing, and scum may be produced, or the smoothness may be lowered.

  Moreover, this invention includes the process of mix | blending a base component (A), acidic phosphate ester (C), and a component (D), mixing and stirring, The acidic hydroxyl group of the said acidic phosphate ester (C) The component (D) has a molar ratio of 100/5 to 100/95, and the total weight ratio of the acidic phosphate ester (C) and the component (D) in the entire treatment agent is 0.001 to 0.001. It can also be expressed as a method for producing a polyurethane elastic fiber treatment agent of 60% by weight.

The viscosity of the treatment agent of the present invention (25 ° C.) is preferably 3~3,000mm ² / s, more preferably ^{5~1,500mm 2 / s, 8~500mm 2 /} s is particularly preferred. If it is less than 3 mm ² / s, volatilization of the treating agent may be a problem, and if it exceeds 3,000 mm ² / s, the polyurethane elastic fiber may be taken by a roller to cause thread trimming.

[impurities]
Trace metals such as Fe, Al, and Si contained in the treatment agent of the present invention are preferably 500 ppm or less, more preferably 200 ppm or less, and particularly preferably 100 ppm or less. These trace metals are Group 2 element metal hydroxides, Group 2 element metal oxides, Group 2 element metal carbonates used in the reaction with the base component and acidic hydroxyl group of acidic phosphate ester (C), It is thought that it mixes from a group 2 element metal. When these impurities exceed 500 ppm, scum may be produced in post-processing.

[Polyurethane elastic fiber]
The polyurethane elastic fiber of the present invention is a polyurethane elastic fiber in which the treatment agent of the present invention is added to the polyurethane elastic fiber main body in an amount of 0.1 to 15% by weight, preferably 1 to 10% by weight. If it is less than 0.1% by weight, the effect of the present invention is not sufficient, and if it exceeds 15% by weight, it is uneconomical. A known method can be adopted as the providing method.

  The polyurethane elastic fiber (elastic fiber main body) of the present invention is a fiber having elasticity using polyether polyurethane or polyester polyurethane.

  The polyurethane elastic fiber of the present invention is prepared by preparing polytetramethylene glycol (PTMG) having a molecular weight of 1000 to 3000 and diphenylmethane diisocyanate (MDI), and dimethyl at PTMG / MDI = 1/2 to 1 / 1.5 (molar ratio). Dry spinning a 20-40% solution of polyurethaneurea polymer obtained by reacting in a solvent such as acetamide or dimethylformamide and reacting with 80-100% of excess isocyanate with a diamine such as ethylenediamine or propanediamine. Polyurethane urea elastic fibers that can be produced by spinning at a spinning speed of 400 to 1000 m / min are preferred.

  The treatment agent of the present invention is preferably used for fibers having a polyurethane elastic fiber having a fineness of 5 to 40 dtex. As a use of the polyurethane elastic fiber of the present invention, it can be used as a fabric by processing yarn such as covering yarn such as CSY, single covering, PLY and air covering, circular knitting, tricot and the like. In addition, these processed yarns and fabrics are used to impart elasticity to products that require elasticity such as stockings, socks, underwear, and swimwear, and outerwear such as jeans and suits for comfort. Also used for purposes. More recently, it has been applied to disposable diapers.

  EXAMPLES The present invention will be specifically described below with reference to examples, but the present invention is not limited to the examples described herein. The percent (%) and part shown in the following examples indicate “% by weight” and “part by weight” unless otherwise specified. Each characteristic in the examples was evaluated according to the following method.

[Method for evaluating treatment agent]
(viscosity)
Using a Canon Fenceke viscometer, the kinematic viscosity of the sample solution at a constant temperature (25 ° C.) was measured.

(Acid value)
Samples dissolved in a solvent such as isopropyl alcohol, xylene / isopropyl alcohol (1/1) mixture, etc., were used with 0.1N potassium hydroxide ethylene glycol isopropyl alcohol solution using an automatic potentiometric titrator (COM-900 manufactured by Hiranuma). Then, potentiometric titration was performed, and the titer (ml) at the end point of neutralization was measured, and the acid value was calculated from Equation (4). The acid value is represented by the number of mg of KOH required to neutralize 1 g of the sample.
Acid value (KOHmg / g) = (A × F × 5.61) / W Formula (4)
(In Formula (4), A = titer (ml), F = 0.1N potency of potassium hydroxide, W = sample weight (g))

(Roller static electricity)
In FIG. 1, the polyurethane elastic fiber cheese (1) provided with a treatment agent is set on the unwinding side of the unwinding speed ratio measuring machine, rotated at a peripheral speed of 50 m / min, and at 2 cm above the cheese, Kasuga The generated static electricity 1 hour after the start of rotation is measured with the formula potentiometer (2).

(Knitting tension)
In FIG. 2, a polyurethane elastic yarn (4) vertically taken from cheese (3) is passed through a compensator (5), a roller (6), and a roller attached to a U gauge (8) via a knitting needle (7) ( 9) is connected to the speedometer (10) and the winding roller (11). The rotational speed of the take-up roller is adjusted so that the traveling speed of the speedometer (10) becomes a constant speed (for example, 10 m / min, 100 m / min), and the knitting tension at that time is taken up by the take-up roller. Is measured with a U gauge (8), and the friction (g) between the fibers / knitting needles is measured. The generated static electricity is measured with a Kasuga-type potentiometer (12) at a distance of 1 cm from the running yarn.

(Friction coefficient between fibers (F / FμS))
In FIG. 3, a monofilament of polyurethane elastic fiber provided with a treatment agent is taken about 50 to 60 cm, a load T1 (13) is suspended at one end, and the other is attached to the U gauge (15) via a roller (14). The secondary tension T2 at that time is measured with a U gauge (15), and the inter-fiber friction coefficient is obtained by Equation (5).
Friction coefficient (F / FμS) = 1 / θ · ln (T2 / T1) Formula (5)
(In Formula (5), θ = 2π, ln = natural logarithm, T1 is 1 g per 22 dtex)

(Unwinding speed ratio)
In FIG. 4, a cheese (16) of polyurethane elastic fiber provided with a treatment agent is set on the unwinding side of the unwinding speed ratio measuring machine, and a paper tube (17) is set on the winding side. After setting the winding speed to a constant speed, the rollers (18) and (19) are activated simultaneously. In this state, there is almost no tension on the yarn (20), so the yarn is stuck on the cheese and does not leave, so the unwinding point (21) is in the state shown in FIG. By changing the unwinding speed, the unwinding point (21) of the yarn (20) from the cheese changes, so the unwinding speed is set so that this point coincides with the contact point (22) between the cheese and the roller. The unraveling speed ratio is obtained by Equation (6). The smaller this value is, the better the unpacking property is.
Unwinding speed ratio (%) = (Winding speed−Unwinding speed) ÷ Unwinding speed × 100 Formula (6)
From the cheese surface layer, the unwinding speed ratio measured in the layer 1 cm inside is taken as the unwinding speed ratio of the outer layer part, and the unwinding speed ratio measured in the layer left 1 cm from the cheese paper tube is the unwinding of the innermost layer part. The speed ratio was used. The smaller the difference in the unwinding speed ratio between the outer layer portion and the innermost layer portion, the better the uniform unwinding property.

(Scum)
In FIG. 4, a string of polyurethane elastic fibers (16) provided with a treatment agent is set on the delivery side, and a paper tube (17) is set on the winding side. After setting the speed of the feeding roller (18) to 100 m / min and the speed of the winding roller (19) to 200 m / min, the feeding roller (18) and the winding roller (19) are started simultaneously. After running for 1 hour, the presence or absence of scum accumulation on the delivery roller (18) is visually determined according to the following criteria.
○: No scum, Δ: Small amount of scum adhering, ×: Adhering scum

(Thread strength)
In FIG. 5, 20 cm of a polyurethane elastic fiber was taken from cheese, applied to a U gauge (8), pulled at a constant speed of 20 cm / min until it was cut, and the load at break (yarn strength) was measured.

(Water content, inorganic salt content)
The water content and the inorganic salt content of the acidic phosphate ester salt (B), the treating agent of the example, and the treating agent of the comparative example were measured by Karl Fischer method and ion chromatograph, respectively.

(Production of acidic phosphate ester salt)
A specific example of the acidic phosphate ester salt A-1 in Table 1 is shown as a method for producing the acidic phosphate ester salt. Isooctyl alcohol and anhydrous phosphoric acid P ₂ O ₅ were reacted at a molar ratio of 1: 0.35 at 80 to 110 ° C. for 4 hours to obtain isooctyl phosphate ester (A-1P in Table 2). The resulting isooctyl phosphate ester had an acid value of 324 (KOH mg / g), and the molar ratio of phosphate monoester to phosphate diester was 40/60.
After adding Mg (OH) ₂ which is a hydroxide of group 2 element metal Mg to the obtained isooctyl phosphate ester, neutralization reaction was performed, and dehydration treatment was performed. Ester salt A-1 was obtained. The molar ratio (H) of the acidic hydroxyl group in the acidic phosphate ester salt A-1 and the molar ratio (I) of the divalent cation Mg ²⁺ of the group 2 element metal are (H) / (I) = 80/20 Met.
As raw materials, the acid phosphate ester shown in Table 2 and the hydroxide of Group 2 element metal shown in Table 1 are used for neutralization reaction so that the molar ratio of acidic hydroxyl group and divalent cation shown in Table 1 is reached. Except for the above, acidic phosphate ester salts A-2 to A-6 used in Examples shown in Table 1 and B-1 to B-2 used in Comparative Examples were obtained by the same production method.

A specific example is shown about acidic phosphate ester salt A-7. Polyoxyethylene 15 mol addition isocetyl ether and phosphoric anhydride P ₂ O ₅ were reacted at a molar ratio of 1: 0.25 at 80 to 110 ° C. for 3 hours to obtain polyoxyethylene 15 mol addition isocetyl ether phosphate. Obtained. The acid value of the obtained polyoxyethylene 15 mol addition isocetyl ether phosphate was 51 (KOHmg / g), and the molar ratio of phosphate monoester to phosphate diester was 25/75.
The obtained polyoxyethylene 15 mol addition isocetyl ether phosphate is added with CaCO ₃ which is a carbonate of group 2 element metal, neutralized by decarboxylation at 80 to 115 ° C., and acid phosphate ester salt A -7 was obtained. The molar ratio (H) of the acidic hydroxyl group and the molar ratio Ca ²⁺ (I) of the divalent cation of the Group 2 element metal in the obtained acidic phosphate ester salt A-7 is (H) / (I) = 35/65 Met.
As raw materials, an acidic phosphate ester shown in Table 2 and a carbonate of a Group 2 element metal shown in Table 1 were used for neutralization reaction so that the molar ratio of the acidic hydroxyl group and divalent cation shown in Table 1 was reached. Except that, acidic phosphate ester salt A-8 used in Examples shown in Table 1 was obtained by the same production method.

表２中の区分は各々、表１中の区分と対応している。すなわち、表２中の区分Ａ−１Ｐは表１中の区分Ａ−１の原料として用いられる酸性リン酸エステルを示す。

Each category in Table 2 corresponds to a category in Table 1. That is, section A-1P in Table 2 shows an acidic phosphate ester used as a raw material of section A-1 in Table 1.

[Examples 1 to 5 and Comparative Examples 1 to 3]
(Adjustment of spinning dope)
A polytetramethylene ether glycol having a number average molecular weight of 2000 was reacted with 4,4′-diphenylmethane diisocyanate at a molar ratio of 1: 2. Subsequently, chain extension was performed using a 1,2-diaminopropane dimethylformamide solution to obtain a dimethylformamide solution having a polymer concentration of 27%. The concentration at 30 ° C. was 1500 mPaS.

The polyurethane spinning dope was discharged into a 190 ° C. N ₂ stream and dry-spun. During spinning, 6% by weight of the treatment agent shown in Table 3 was applied to the fiber by an oiling roller. Then, it wound up on the bobbin at a speed | rate of 500 m / min, and obtained 77 dtex monofilament cheese (400 g of winding amounts). The obtained cheese was left for 48 hours in an atmosphere of 35 ° C. and 50% RH for evaluation. The evaluation results of the treatment agent performance are shown in Table 3. In addition, a processing agent mix | blends each component of Table 3, and mixes and stirs it (the compounding quantity in a table | surface is a weight part), and is prepared. The acidic phosphate ester salts in Tables 3 to 5 are as shown in Table 1. H / I in Tables 3 to 5 indicates the molar ratio (H) / (I) of the acidic hydroxyl group and the divalent cation of the Group 2 element metal in the acidic phosphate ester salt.

[Examples 6 to 10 and Comparative Examples 4 to 5]
In the same manner as in Examples 1 to 5, the polyurethane spinning stock solution was discharged into a 190 ° C. N ₂ air stream and dry-spun. During spinning, 6% by weight of the treatment agent described in Table 4 was applied to the fiber by an oiling roller. After that, it was wound on a bobbin at a speed of 500 m / min to obtain 44 dtex monofilament cheese (wound amount 400 g). The obtained cheese was left for 48 hours in an atmosphere of 35 ° C. and 50% RH for evaluation. These results are shown in Table 4. In addition, a processing agent mix | blends each component of Table 4, and mixes and stirs it (the compounding quantity in a table | surface is a weight part), and prepares it.

[Examples 11 to 15 and Comparative Examples 6 to 8]
(Adjustment of spinning dope)
100 parts by weight of polytetramethylene glycol having a number average molecular weight of 2000 and 25 parts by weight of 4,4′-diphenylmethane diisocyanate are reacted at 70 ° C., and 250 parts by weight of N, N′-dimethylacetamide is added to dissolve the reaction mixture while cooling. It was. A solution prepared by dissolving 5 parts by weight of 1,2-diaminopropane in 184 parts by weight of N, N′-dimethylacetamide was added, and 0.2% by weight of dimethyl silicone (10000 mm ² / s) was added.

The polyurethane spinning dope was discharged from a spinneret having four pores into a 180 ° C. N ₂ stream and dry-spun. During spinning, 6% by weight of the treatment agent listed in Table 5 was applied to the fiber by an oiling roller. Then, the bobbin was wound up at a speed of 500 m / min to obtain 22 dtex multifilament cheese (rolling amount 400 g). The obtained cheese was left for 48 hours in an atmosphere of 35 ° C. and 50% RH for evaluation. These results are shown in Table 5. In addition, a processing agent mix | blends each component of Table 5, and mixes and stirs it (the compounding quantity in a table | surface is a weight part), and prepares it.

[Examples 16 to 20 and Comparative Examples 9 to 10]
In the same manner as in Examples 6 to 10, the polyurethane spinning stock solution was discharged into a 190 ° C. N ₂ gas stream and dry-spun. During spinning, 6% by weight of the treatment agent shown in Table 7 was applied to the fiber by an oiling roller. After that, it was wound on a bobbin at a speed of 500 m / min to obtain 44 dtex monofilament cheese (wound amount 400 g). The obtained cheese was left for 48 hours in an atmosphere of 35 ° C. and 50% RH for evaluation. These results are shown in Table 7. In addition, a processing agent mix | blends each component of Table 7, and mixes and stirs it (the compounding quantity in a table | surface is a weight part), and prepares it. The acid phosphate esters (C) in Tables 7 and 8 are as described in Table 2. The formula weights and reactive group values of the components (D) in Tables 7 and 8 are as shown in Table 6. (P) in Tables 7 and 8 indicates (P) at a molar ratio of 100 / (P) between the acidic hydroxyl group of the acidic phosphate ester (C) and the component (D).

[Examples 21 to 22 and Comparative Examples 11 to 14]
In the same manner as in Examples 11 to 15, the polyurethane spinning dope was discharged into a 180 ° C. N ₂ stream and dry-spun. During spinning, 6% by weight of the treatment agent shown in Table 8 was applied to the fiber by an oiling roller. Then, 22 dtex monofilament cheese (wound amount 400g) was wound on a bobbin at a speed of 500 m / min. The obtained cheese was left for 48 hours in an atmosphere of 35 ° C. and 50% RH for evaluation. These results are shown in Table 8. In addition, a processing agent mix | blends each component of Table 8, and mixes and stirs it (the compounding quantity in a table | surface is a weight part), and prepares it.

Various physical properties of the components described in Tables 3 to 8 are shown below. The viscosity was measured at 25 ° C.
1) Base component (A)
Dimethyl silicone (viscosity 5 mm ² / s): average molecular weight 700
Dimethyl silicone (viscosity 15 mm ² / s): average molecular weight 2000
Dimethyl silicone (viscosity 10 mm ² / s): average molecular weight 1000
Liquid paraffin 40 seconds: mineral oil, viscosity 6.4 mm ² / s
Liquid paraffin 60 seconds: mineral oil, viscosity 15.7 mm ² / s
Liquid paraffin 80 seconds: mineral oil, viscosity 21.8 mm ² / s
Isooctyl laurate: ester oil, viscosity 7.3 mm ² / s
Isooctyl stearate: ester oil, viscosity 15.2 mm ² / s
Isooctyl palmitate: ester oil, viscosity 13.1 mm ² / s
2) Other components Potassium stearyl phosphate: completely neutralized product, acid value 0 KOH mg / g
Magnesium distearate: 99%, 200-mesh product Dioctylsulfosuccinate Na: completely neutralized product, acid value 0 KOH mg / g
Isodecyl phosphate: acid value 300KOHmg / g
Amino-modified silicone KF-880: viscosity 650 mm ² / s, amino equivalent 1800 g / mol, amine value 30 KOH mg / g, manufactured by Shin-Etsu Chemical Co., Ltd. polyether-modified silicone KF-351: viscosity 100 mm ² / s, manufactured by Shin-Etsu Chemical MQ Silicone resin TSF 4600: viscosity 700 mm ² / s, manufactured by Momentive Performance Materials Japan GK Isotridecyl phosphate potassium: 40% neutralization of isotridecyl phosphate (A-5P) described in Table 2 object

  The treatment agent of the present invention is suitably used when producing polyurethane elastic fibers. The polyurethane elastic fiber of the present invention has a stable and excellent anti-sticking property, uniform unwinding property, antistatic property, smoothness and productivity.

DESCRIPTION OF SYMBOLS 1 Polyurethane elastic fiber cheese 2 Kasuga-type potentiometer 3 Polyurethane elastic fiber cheese 4 Polyurethane elastic yarn 5 Compensation sweater 6 Roller 7 Knitting needle 8 U gauge 9 Roller 10 Speedometer 11 Winding roller 12 Kasuga-type potentiometer 13 Load 14 Roller 15 U gauge 16 Cheese 17 Winding paper tube 18 Roller 19 Roller 20 Traveling yarn 21 Unwinding point 22 Contact point of cheese and roller

Claims (9)

Containing at least one base component (A) selected from silicone oil, mineral oil and ester oil, and an acidic phosphate ester salt (B) of a divalent cation of a Group 2 element metal,
The acidic phosphate ester salt (B) has an acidic hydroxyl group, and the molar ratio of the acidic hydroxyl group to the divalent cation of the Group 2 element metal is 95/5 to 5/95,
The processing agent for polyurethane elastic fibers whose weight ratio of the said acidic phosphate ester salt (B) to the whole processing agent is 0.001 to 60 weight%. The processing agent according to claim 1, wherein the divalent cation of the Group 2 element metal is at least one selected from Be ²⁺ , Mg ²⁺ , Ca ²⁺ , Sr ²⁺ and Ba ²⁺ . The acidic phosphate ester salt is at least selected from an acidic phosphate ester (C), a Group 2 element metal hydroxide, a Group 2 element metal hydroxide, a Group 2 element metal oxide, and a Group 2 element metal carbonate. A product obtained by reacting one component (D);
The processing agent of Claim 1 or 2 whose molar ratio of the acidic hydroxyl group of the said acidic phosphate ester (C) and the said component (D) is 100/5-100/95. The processing agent of Claim 3 whose said acidic phosphate ester (C) is a compound represented by following General formula (1).

(R ¹ in Formula (1) represents a hydrocarbon group having 1 to 30 carbon atoms. X represents an alkylene group having 2 to 4 carbon atoms, and XO represents an oxyalkylene group. A represents an oxyalkylene group. And is an integer of 0 or 1 to 15. b and c are each 1 or 2, and are integers satisfying b + c = 3.) At least one base component (A) selected from silicone oil, mineral oil and ester oil, acidic phosphate ester (C), Group 2 element metal hydroxide, Group 2 element metal hydroxide, Group 2 element metal Comprising at least one component (D) selected from oxides and carbonates of group 2 element metals,
The molar ratio of the acidic hydroxyl group of the acidic phosphate ester (C) to the component (D) is 100/5 to 100/95,
The processing agent for polyurethane elastic fibers whose total weight ratio of the said acidic phosphate ester (C) and the said component (D) which occupies for the whole processing agent is 0.001 to 60 weight%.   The processing agent according to claim 5, wherein the Group 2 element metal is at least one selected from Be, Mg, Ca, Sr and Ba. The processing agent according to claim 5 or 6, wherein the acidic phosphate ester (C) is a compound represented by the following general formula (1).

(R ¹ in Formula (1) represents a hydrocarbon group having 1 to 30 carbon atoms. X represents an alkylene group having 2 to 4 carbon atoms, and XO represents an oxyalkylene group. A represents an oxyalkylene group. And is an integer of 0 or 1 to 15. b and c are each 1 or 2, and are integers satisfying b + c = 3.)   Further contains at least one component selected from alkyl-modified silicone, ester-modified silicone, polyether-modified silicone, carbinol-modified silicone, carboxy-modified silicone, amino-modified silicone, neutralized organophosphate of amino-modified silicone and silicone resin And the processing agent in any one of Claims 1-7 whose weight ratio of this component to the whole processing agent is 0.01 to 10 weight%.   The polyurethane elastic fiber by which 0.1-15 weight% of processing agents in any one of Claims 1-8 are provided to the polyurethane elastic fiber main body.

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