KR100397705B1 - Spandex fiber having improved resistances to discoloration and chlorine - Google Patents

Abstract

The spandex fiber of the present invention is based on the total weight of the segmented polyurethane polymer and the spandex fiber, (A) hindered phenolic compound 0.5 to 3% by weight, (B) 0.2 to 2% by weight of semicarbazide-based compound, (C ) 0.2 to 5% by weight of poly (N, N-diethyl-2-aminoethyl methacrylate), and 1 to 5% by weight of (D) zinc oxide.

Description

Spandex fiber with improved discoloration resistance and chlorine resistance {SPANDEX FIBER HAVING IMPROVED RESISTANCES TO DISCOLORATION AND CHLORINE}

The present invention relates to spandex fibers with improved discoloration and chlorine resistance. More specifically, the present invention includes a hindered phenol compound, a semicarbazide compound, poly (N, N-diethyl-2-aminoethyl methacrylate), and zinc oxide, thereby improving discoloration and chlorine resistance. And stabilized spandex fibers.

Spandex fibers are well known in the art as highly stretchable polyurethane based fibers having more than 85% by weight of urethane bonds. Spandex fibers generally include a spinning yarn which extrudes a spinning solution containing polyurethane through a nozzle and introduces a heating gas for evaporating and drying the solvent; Wet spinning to solidify the polymer while eluting the solvent through a spinning bath; Chemical spinning which extrudes a prepolymer solution having isocyanates in a reaction solution containing an amine chain extender through a nozzle for chain extension reaction; Alternatively, the polyurethane is manufactured through melt spinning, which is extruded through a nozzle in a molten state and cooled.

In laundry and use, maintaining durability and whiteness are important properties for spandex, and many attempts have been made to prevent or reduce damage to yellowing and mechanical properties caused by exposure of spandex fibers to various environmental factors. . For example, US Pat. No. 2,999,839 discloses segmented polyurethane compositions comprising methacrylates comprising tertiary amines and methods of making the same. However, the addition of methacrylates containing such tertiary amines to the spandex fibers can prevent discoloration by ultraviolet and atmospheric gases, but leads to discoloration and deterioration of physical properties when exposed to chlorine water.

In addition, yarns of spandex fibers are particularly useful for the manufacture of swimwear, in which case the polyurethane spandex fibers are chlorinated to such an extent that the amount of active chlorine in the pool water is 0.5 to 3 ppm or more. Exposure resulted in damage to the physical properties of the fibers. Thus, there is a need for resistance to damage due to such chlorine water, especially for low denier spandex fibers of less than 100 denier. U.S. Patent No. 4,340,527 discloses adding zinc oxide to provide chlorine resistance to spandex. However, although zinc oxide can improve the chlorine resistance of spandex, it is not effective for discoloration resistance.

WO 00/36195 discloses poly (N, N-diethyl-2-aminoethyl methacrylate), and zinc oxide or huntite and hydromagnesite, respectively, to impart discoloration and chlorine resistance. Spandex to which a mixture of (hydromagnesite) is added is disclosed. However, by using poly (N, N-diethyl-2-aminoethyl methacrylate) and a chlorine resistant agent at the same time, a synergistic effect of discoloration and chlorine resistance was desired, but the effect was not large.

Accordingly, an object of the present invention is to add a hindered phenol compound, a semicarbazide compound, poly (N, N-diethyl-2-aminoethyl methacrylate) and zinc oxide to the spandex fiber together, It is to provide a stabilized spandex fiber, which is prevented from discoloration and deterioration by atmospheric smog gas, heat and chlorine water.

The above and other objects of the present invention can be achieved by the following description. Hereinafter, the content of the present invention will be described in detail.

The spandex fiber of the present invention is based on the total weight of the segmented polyurethane polymer and the spandex fiber, (A) hindered phenolic compound 0.5 to 3% by weight, (B) 0.2 to 2% by weight of semicarbazide-based compound, (C ) 0.2 to 5% by weight of poly (N, N-diethyl-2-aminoethyl methacrylate) and 1 to 5% by weight of (D) zinc oxide. This will be described in detail as follows.

The weight percentages here are based on the weight of the spundex yarn spun.

The segmented polyurethane polymers used in the spandex fibers of the present invention react with organic diisocyanates and polymer diols to prepare polyurethane precursors, and then dissolve them in organic solvents and then react with diamines and monoamines, as known in the art. It is prepared by making.

The organic diisocyanate used in the present invention includes diphenylmethane-4,4'-diisocyanate, hexamethylene diisocyanate, toluene diisocyanate, butylene diisocyanate, hydrogenated P, P-methylene diisocyanate and the like. As the polymer diol, polytetramethylene ether glycol, polypropylene glycol, polycarbonate diol, and the like may be used. The diamines are used as chain extenders, and examples thereof include ethylenediamine, propylenediamine, hydrazine, and the like. In addition, the monoamine is used as a chain terminator, and examples thereof include diethylamine, monoethanolamine, dimethylamine, and the like.

(A) Hindered phenolic compound

The hindered phenolic compound (B) used in the spandex fiber of the present invention is applied together with the other additives of the present invention to have an excellent effect in improving the discoloration resistance and chlorine resistance of the spandex. Preferred examples of the hindered phenol compound (A) include ethylene bis (oxyethylene) bis- (3- (5-t-butyl-4-hydroxy-m-toyl) -propionate) or 3,9 -Bis (2- (3- (3-t-butyl-4-hydroxy-5-methylphenyl) propionyloxy) -1,1-dimethylethyl) 2,4,8,10-tetraoxaspiro [5, 5] There is Undecan.

(B) Semicarbazide Compound

The semicarbazide-based compound (B) used in the spandex fibers of the present invention provides discoloration resistance of the spandex to atmospheric smog gas. It can also be applied to spandex together with the polymer component (C) of the present invention to impart a synergistic effect with discoloration and chlorine resistance to atmospheric smog. Preferred examples of the semicarbazide-based compound (B) include 1,1,1 ', 1'-tetramethyl-4,4' (methylene-di-p-phenylene) dicemicarbazide and biuretri-tree ( Hexamethylene-N, N-dimethylsemicarbazide) or 1,6-hexamethylenebis (N, N-dimethylsemicarbazide). Of these, 1,1,1 ', 1'-tetramethyl-4,4' (methylene-di-p-phenylene) disemicarbazide is most preferred.

(C) poly (N, N-diethyl-2-aminoethyl methacrylate)

The poly (N, N-diethyl-2-aminoethyl methacrylate) (C) used in the spandex fibers of the present invention is applied with other additives of the present invention to improve the discoloration and chlorine resistance of the spandex. Has an effect.

(D) zinc oxide

The zinc oxide (D) used for the spandex fiber of the present invention preferably has a particle size of 1 m or less. If the particle size is 1 μm or more, a problem of shortening the cycle of replacing the spin filter occurs. The zinc oxide is used as a chlorine resistant agent.

The spandex fiber of the present invention may further include additives such as titanium dioxide, magnesium stearate and the like in addition to the main components. The titanium dioxide may be used in the range of 0.1 to 5 wt% based on the whiteness of the spandex based on the total weight of the spandex fiber. Titanium dioxide is in the form of anatase and rutile, and it is preferable to use a rutile form which is excellent in whiteness and UV absorption. In addition, the magnesium stearate may be used in the range of 0.1 to 2% by weight based on the total weight of the spandex fiber, which is added to improve the adhesion and disintegration of the spandex.

The additives added to the spandex fibers of the present invention do not exhibit the properties of the present invention below a given range of content, and remain equal without exceeding the effects of the present invention over a given range of content.

The spandex fibers of the present invention can be prepared by adding the above (A) to (D) components in the specified amounts to the segmented polyurethane polymers synthesized by known methods, and then spinning by conventional methods.

The invention can be better understood by the following examples, which are intended for the purpose of illustration of the invention and are not intended to limit the scope of protection defined by the appended claims.

Example

Preparation of Segment Polyurethane Polymer

518 g of diphenylmethane-4,4'-diisocyanate and 2328 g of polytetramethylene ether glycol (molecular weight 1,800) were reacted with stirring at 80 ° C. for 90 minutes in a nitrogen gas stream to prepare a polyurethane precursor containing isocyanate at both ends. It was. After the polyurethane precursor was cooled to room temperature, 4643 g of dimethylacetamide was added thereto and dissolved to obtain a polyurethane precursor solution. Subsequently, a solution obtained by dissolving 54 g of propylenediamine and 9.1 g of diethylamine in 1889 g of dimethylacetamide was added to the polyurethane precursor solution at 10 ° C. or lower to prepare a segmented polyurethane polymer solution.

Preparation of Spandex Fiber

(A) hindered phenolic compound, (B) semicarbazide-based compound, (C) poly (N, N-diethyl-) used in the spandex fibers of Examples 1 to 2 and Comparative Examples 1 to 3 below 2-aminoethyl methacrylate) and (D) zinc oxide were prepared and specifications were as follows.

(A) Hindered phenolic compound

(a ₁ ) ethylenebis (oxyethylene) bis- (3- (5-t-butyl-4-hydroxy-m-toyl) -propionate): Irganox 245, Ciba

(a ₂ ) 3,9-bis (2- (3- (3-t-butyl-4-hydroxy-5-methylphenyl) propionyloxy) -1,1-dimethylethyl) 2,4,8,10 Tetraoxaspiro [5,5] Undecan: GA-80 (Sumitomo, Japan)

(B) Semicarbazide Compound

1,1,1 ', 1'-tetramethyl-4,4' (methylene-di-p-phenylene) dicemicarbazide: HN-150 (Hydrazine Industry Co., Ltd.)

(C) Poly (N, N-diethyl-2-aminoethyl methacrylate): hemp (SAM, Daesung CT, Korea)

(D) Zinc Oxide: Kadox 911, Zinc Corporation of America

(E) Condensation polymers of p-cresol and divinylbenzene: methacrorol (Methacrol 2390 ^R D, Dupont, USA)

Using the above-described segmented polyurethane polymer and the above-mentioned constituents, spandex fibers were prepared as shown in Table 1 below.

division Example (Unit: wt%) Comparative Example (Unit: wt%) One 2 One 2 3 (A) Hindered phenolic compound (a ₁ ) ethylenebis (oxyethylene) bis- (3- (5-t-butyl-4-hydroxy-m-toyl) -propionate) 1.5 - - 1.5 - (a ₂ ) 3,9-bis (2- (3- (3-t-butyl-4-hydrogroup-5-methylphenyl) propionyloxy) -1,1-dimethylethyl) 2,4,8,10 Tetraoxaspiro [5,5] Undecan - 1.5 - - - (B) Semicarbazide Compound 1.0 1.0 1.0 - - (C) poly (N, N-diethyl-2-aminoethyl methacrylate) 1.0 1.0 1.0 1.0 0.58 (D) zinc oxide 3.0 3.0 3.0 3.0 3.0 (E) Condensation polymer of p-cresol and divinylbenzene - - - - 1.5

The polyurethane spinning stock solution was prepared by mixing the components of Examples 1 to 2 and Comparative Examples 1 to 3 shown in Table 1 with 0.1 wt% of titanium dioxide and 0.5 wt% of magnesium stearate.

After degassing this spinning stock solution, 4 filament 40 denier elastic yarns were prepared by adjusting the spinning temperature to 250 ° C. in a dry spinning process. The elastic yarn thus obtained was spundex circular knitted fabric as a specimen using a circular knitting machine (KT-400, 4 inches in diameter, 400 submerged, Nagakaseiki, Japan), wherein the length of the sample was 10 cm. . Subsequently, 2 g / l of UNITOL CT-81 (Non-Curable, Korea), which is a nonionic surfactant, and 3 g / l of UNITOL-SMS (Non-Curable, Korea), which is a nonionic emulsifier, were mixed and used as a refining agent. The spandex circular knitted fabric was refined using the refining method. The physical properties of the circular knitted sample were measured by the following method.

Property evaluation

(1) UV test

The UV test was performed using an accelerated weathering tester (Q-Panel, USA), and a UV-B lamp was used as the UV lamp. The temperature was fixed at 60 ° C. and the sample was treated for 24 hours at this temperature.

Before and after the sample was processed, the "b" value (yellowing value) of the sample was measured by Color-view (Gardener, USA), respectively. The difference between the b value after sample treatment and the b value before treatment was represented by Δb.

(2) NO _X gas test

To evaluate the resistance to NO _X gas, NOx gas generating solution was prepared from a mixed solution consisting of 300 mL of ion-exchanged water, 8 mL of 85% aqueous phosphate solution, and 40 mL of sodium acetate (NaNO ₂ ) (10 g / L). The solution was placed in a sealed container and the sample was treated with NOx gas at room temperature for 24 hours.

Before and after the sample was processed, the "b" value (yellowing value) of the sample was measured by Color-view (Gardener, USA), respectively. The difference between the b value after sample treatment and the b value before treatment was represented by Δb.

(3) chlorine resistance test

For the evaluation of chlorine resistance, the sample was immersed in 30 L of chlorine water with an effective chlorine amount of 3 ppm and pH = 7.0 for 72 hours at room temperature. Chlorine water was continuously circulated through the stirrer during testing, and the amount of effective chlorine in the chlorine water was controlled by sodium hypochlorite (NaClO) and measured by the ASTM D1291 method.

Before and after the sample was processed, the "b" value (yellowing value) of the sample was measured by Color-view (Gardener, USA), respectively. The difference between the b value after sample treatment and the b value before treatment was represented by Δb.

(4) Strength retention test in chlorine water

For evaluation of the strong retention in chlorine water, spandex yarn was immersed at 50% elongation in chlorine water with an effective amount of chlorine 3 ppm, pH = 7.0 for 72 hours at room temperature. Intensity assessment was performed using Instron 4301 (Instron, USA). At this time, the length of the sample was 5 cm, 1 kg of cells (Cell) was used, and the cross head speed was maintained at 300 mm / min.

Strong retention was calculated by the following equation:

(S _o : Strong before treatment, S: Strong after treatment)

These physical property measurement results are summarized in Table 2 below.

Ultraviolet (Δb) Heat resistance (Δb) NO _X gaseous (Δb) Chlorine Tolerance (Δb) / Strength Retention Rate Example One 3.2 5.9 7.1 4.0 / 82 2 3.3 5.7 7.4 4.2 / 83 Comparative Example One 4.0 14.4 8.0 6.0 / 77 2 6.2 7.4 14.5 7.1 / 74 3 4.2 12.4 9.2 7.2 / 75

In Table 2, the smaller the Δb value indicating resistance to ultraviolet rays, heat, NO _x gas and chlorine, the better the property. As can be seen in the Examples and Comparative Examples of Table 2, the spandex fiber of the present invention is excellent in resistance to NO _x gas, which is the main component of ultraviolet and atmospheric smog, small discoloration in chlorine water, high strength It can be seen.

The spandex fiber of the present invention comprises a hindered phenol compound, a semicarbazide compound, poly (N, N-diethyl-2-aminoethyl methacrylate) and zinc oxide together, thereby providing ultraviolet light, atmospheric smog gas and chlorine. Discoloration of the water is prevented.

Simple modifications and variations of the present invention can be easily made by those skilled in the art, and all such modifications or changes can be seen to be included in the scope of the present invention.

Claims (3)

Based on Segment Polyurethane Polymer, and Spandex Fiber Total Weight (A) 0.5 to 3% by weight of the hindered phenolic compound; (B) 0.2 to 2 wt% of semicarbazide compounds; (C) 0.2 to 5% by weight of poly (N, N-diethyl-2-aminoethyl methacrylate); And (D) 1 to 5 wt% zinc oxide Characterized in that it comprises a spandex fiber. The method of claim 1, The hindered phenolic compound (A) is ethylenebis (oxyethylene) bis- (3- (5-t-butyl-4-hydroxy-m-toyl) -propionate) or 3,9-bis (2 -(3- (3-t-butyl-4-hydroxy-5-methylphenyl) propionyloxy) -1,1-dimethylethyl) 2,4,8,10-tetraoxaspiro [5,5] undecane Spandex fiber characterized by the above-mentioned. The method of claim 1, The semicarbazide-based compound (B) is 1,1,1'1'-tetramethyl-4,4 '(methylene-di-p-phenylene) diisemicarbazide, biuretri-tri (hexamethylene-N , N-dimethylsemicarbazide) or 1,6-hexamethylenebis (N, N-dimethylsemicarbazide), spandex fiber.