KR100580325B1 - A polyurethaneurea elastic fiber with excellent dyeing property and light resistance, and a process of preparing the same - Google Patents

A polyurethaneurea elastic fiber with excellent dyeing property and light resistance, and a process of preparing the same Download PDF

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KR100580325B1
KR100580325B1 KR1020040111713A KR20040111713A KR100580325B1 KR 100580325 B1 KR100580325 B1 KR 100580325B1 KR 1020040111713 A KR1020040111713 A KR 1020040111713A KR 20040111713 A KR20040111713 A KR 20040111713A KR 100580325 B1 KR100580325 B1 KR 100580325B1
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elastic fiber
light resistance
polyurethane urea
dyeing
polyurethaneurea
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KR1020040111713A
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Korean (ko)
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이창배
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주식회사 코오롱
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    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/58Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products
    • D01F6/70Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyurethanes
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F1/00General methods for the manufacture of artificial filaments or the like
    • D01F1/02Addition of substances to the spinning solution or to the melt
    • D01F1/10Other agents for modifying properties
    • D01F1/106Radiation shielding agents, e.g. absorbing, reflecting agents
    • DTEXTILES; PAPER
    • D10INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10BINDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10B2331/00Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products
    • D10B2331/10Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products polyurethanes
    • DTEXTILES; PAPER
    • D10INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10BINDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10B2401/00Physical properties
    • D10B2401/06Load-responsive characteristics
    • D10B2401/061Load-responsive characteristics elastic
    • DTEXTILES; PAPER
    • D10INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10BINDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10B2401/00Physical properties
    • D10B2401/14Dyeability
    • DTEXTILES; PAPER
    • D10INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10BINDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10B2401/00Physical properties
    • D10B2401/22Physical properties protective against sunlight or UV radiation

Abstract

본 발명은 폴리우레탄우레아 탄성섬유 및 그의 제조방법에 관한 것으로서, 폴리우레탄우레아 중합체 용액을 방사하여 폴리우레탄우레아 탄성섬유를 제조함에 있어서, 상기 중합체 용액에 3급 아민을 포함하는 디에스테르 화합물을 첨가하는 것을 특징으로 한다. 본 발명은 방사중 첨가제 조성물의 열취하로 인한 공정장애를 효과적으로 방지 할 수 있다. 본 발명의 섬유는 염색성 및 내광성이 매우 우수하다.The present invention relates to a polyurethane urea elastic fiber and a method of manufacturing the same, in the manufacture of a polyurethane urea elastic fiber by spinning a polyurethane urea polymer solution, adding a diester compound containing a tertiary amine to the polymer solution It is characterized by. The present invention can effectively prevent the process failure due to heat withdrawal of the additive composition during spinning. The fiber of the present invention is very excellent in dyeing and light resistance.

탄성섬유, 폴리우레탄우레아, 염색성, 자외선안정제, 내광성, 디에스테르 화합물, 3급 아민.Elastic fiber, polyurethaneurea, dyeing, UV stabilizer, light resistance, diester compound, tertiary amine.

Description

염색성 및 내광성이 우수한 폴리우레탄우레아 탄성섬유 및 그의 제조방법 {A polyurethaneurea elastic fiber with excellent dyeing property and light resistance, and a process of preparing the same}A polyurethaneurea elastic fiber with excellent dyeing property and light resistance, and a process of preparing the same}

본 발명은 염색성 및 내광성이 우수한 폴리우레탄우레아 탄성섬유 및 그의 제조방법에 관한 것이다. The present invention relates to a polyurethaneurea elastic fiber excellent in dyeing and light resistance, and a manufacturing method thereof.

보다 구체적으로는 산화방지제, 방사성 향상제, 소광제 및 백도제 등으로 구성되는 공지의 첨가제 조성물에 새로운 형태의 화합물 조성을 첨가하여, 방사중 첨가제의 열분해로 인한 공정장애를 방지하여 조업성을 개선하고, 탄성섬유의 고유한 물성을 유지하면서도 내후성, 특히 염색성 및 내광성이 우수한 폴리우레탄우레아 탄성섬유를 제조하는 방법에 관한 것이다.More specifically, a new type of compound composition is added to a known additive composition composed of an antioxidant, a radioactive agent, a quencher, and a whitening agent, to improve processability by preventing a process obstacle due to thermal decomposition of the additive during spinning, The present invention relates to a method for producing a polyurethaneurea elastic fiber having excellent weather resistance, particularly dyeing and light resistance, while maintaining the inherent physical properties of the elastic fiber.

통상 폴리우레탄우레아 탄성섬유는 폴리우레탄우레아 중합체를 습식 또는 건식 방사하여 제조된다. 이때 사용되는 폴리우레탄우레아 중합체는 2,000g/몰 수준의 고분자량을 갖는 폴리올, 과량의 디이소시아네이트 및 디올 또는 디아민 화합물인 쇄연장제를 동시에 반응시키는 1단계 중합법으로 제조 할 수 있고, 상기 고분자 량의 폴리올과 과량의 디이소시아네이트를 먼저 예비중합 하여 1단계로 예비중합체를 제조한 다음 여기에 디올 또는 디아민 화합물인 쇄연장제를 투입하여 2단계로 쇄연장 반응시키는 2단계 중합법으로 제조 할 수도 있다.Typically polyurethaneurea elastic fibers are produced by wet or dry spinning a polyurethaneurea polymer. In this case, the polyurethaneurea polymer used may be prepared by a one-step polymerization method of simultaneously reacting a polyol having a high molecular weight of 2,000 g / mol, an excess of diisocyanate and a chain extender, which is a diol or a diamine compound, and the high molecular weight. The polyol and an excess of diisocyanate are first prepolymerized to prepare a prepolymer in one step, and then a chain extender, which is a diol or a diamine compound, may be added thereto to prepare a two-step polymerization process. .

폴리우레탄우레아 탄성섬유는 탄성과 탄성회복력이 우수하여 스타킹이나 여성의 속옷 등에 많이 사용되고 있고, 특히 그의 탄성을 이용하여 운동복이나 수영복 등에 많이 사용되고 있다. 그러나 폴리우레탄우레아 탄성섬유는 대기중에 노출되면 일광에 의하여 탄성섬유 고유의 물성 및 색상이 변하고, 대기중의 폐가스 등에 의해서도 쉽게 변색되며, 또 자연적인 외기에서도 쉽게 산화되어 그의 고유물성이 저하된다. 또한 폴리우레탄우레아 탄성섬유는 구조적으로 산성염료에 염색되지 않는 단점을 가지고 있다.Polyurethane urea elastic fibers are used in stockings and women's underwear because of their excellent elasticity and elastic recovery, in particular, they are widely used in sportswear or swimwear by using their elasticity. However, when the polyurethane urea elastic fiber is exposed to the atmosphere, the physical properties and colors of the elastic fiber change due to sunlight, and are easily discolored by the waste gas in the atmosphere. In addition, polyurethaneurea elastic fiber has a disadvantage that it is not structurally dyed in acid dyes.

이러한 결점들을 보완하기 위하여 대한민국 출원특허 90-10867호에서는 페놀계산화방지제, 아민계 자외선안정제 및 메타아크릴레이트계 염색증진제를 첨가제로 사용하는 방법을 제안하고 있다. 그러나 상기 메타아크릴레이트계 염색증진제는 내열성이 약하여 고온방사시 폴리머 외부로 침출, 승화되어 방사공정에 심각한 문제를 일으키는 단점이 있다. In order to compensate for these drawbacks, Korean Patent Application No. 90-10867 proposes a method of using a phenolic antioxidant, an amine UV stabilizer, and a methacrylate dye enhancer as an additive. However, the methacrylate dye enhancer is weak in heat resistance and has a disadvantage of causing serious problems in the spinning process by leaching and subliming to the outside of the polymer during high temperature spinning.

대한민국 등록특허 제160468호에서는 페놀계 산화방지제, 벤조트리아졸계 광안정제, 힌더드 아민계 자외선안정제, 세미카바자지이드계 내폐가스안정제를 첨가제로 사용하는 방법이 기재되어 있고, 대한민국 특허 공고공보 93-11337호에서는 페놀계 산화방지제, 아인산염계 산화방지제, 세미카바지이드계 황변방지제 및 벤조트리아졸계 광안정제를 사용하여 내후성 탄성섬유를 제조하는 방법을 기술하고 있 으나, 상기 방법들에서 공통적으로 사용되는 벤조트리아졸계 광안정제는 내열성이 부족할 뿐만 아니라 폴리우레탄우레아 중합체와의 상용성이 부족하여 방사시 침출, 승화되어 방사공정에 악영향을 미치게 되는 문제가 있었다.Korean Patent No. 160468 describes a method of using a phenolic antioxidant, a benzotriazole light stabilizer, a hindered amine UV stabilizer, a semicarbazide-based waste gas stabilizer as an additive, and Korean Patent Publication No. 93- 11337 describes a method for producing weather resistant elastic fibers using phenolic antioxidants, phosphite antioxidants, semicarbazide-based yellowing inhibitors and benzotriazole-based light stabilizers, but is commonly used in the above methods. The benzotriazole-based light stabilizer was not only poor in heat resistance, but also lacked in compatibility with the polyurethaneurea polymer, which caused leaching and sublimation during spinning, which adversely affected the spinning process.

대한민국 등록특허 제129113호에서는 폴리우레탄 탄성섬유의 염색성을 향상시키기 위하여 3급 아민을 포함하는 폴리우레탄계 염색증진제를 사용하는 방법을 기술하고 있으나, 상기 방법은 폴리우레탄계 염색증진제의 투입량에 비하여 염색증진 효과가 뛰어나지 못한 단점이 있다.Republic of Korea Patent No. 129113 describes a method of using a polyurethane-based dye enhancer comprising a tertiary amine in order to improve the dyeability of polyurethane elastic fibers, the method is a dye-promoting effect compared to the amount of the polyurethane-based dye enhancer There are disadvantages that are not outstanding.

이상에서 살펴본 바와 같이 폴리우레탄우레아 탄성섬유의 염색성과 내광성을 향상시키기 위하여 여러가지 안정제를 포함한 조합물이 제안되어 왔으나, 장기적으로 방사공정을 안정되게 유지하면서 염색성과 내광성이 우수한 폴리우레탄우레아 탄성섬유를 생산 할 수 있는 기술은 지금까지 개발되지 못하였다.As described above, a combination including various stabilizers has been proposed to improve the dyeing and light resistance of polyurethane urea elastic fibers, but it produces polyurethane urea elastic fibers with excellent dyeing and light resistance while maintaining a stable spinning process in the long term. The technology to do this has not been developed until now.

본 발명의 목적은 새로운 형태의 첨가제를 사용하여 폴리우레탄우레아 탄성섬유의 염색성과 내광성을 획기적으로 개선함과 동시에, 내열성이 약한 첨가제의 열취하로 인해 발생되는 방사공정의 문제점들을 해소하여 장기적으로 안정하게 폴리우레탄우레아 탄성섬유를 제조 할 수 있는 방법을 제공하기 위한 것이다.The purpose of the present invention is to improve the dyeing and light resistance of polyurethaneurea elastic fiber by using a new type of additive, and at the same time, to solve the problems of the spinning process caused by the heat withdrawal of the weak heat-resistant additives, which is stable in the long term. To provide a method for producing a polyurethane urea elastic fiber.

본 발명은 새로운 형태의 첨가제를 사용하여 폴리우레탄우레아 탄성섬유의 염색성과 내광성을 획기적으로 개선함과 동시에, 방사공정 중 첨가제의 열취하로 인해 발생되는 공정 장애를 방지하므로서 폴리우레탄우레아 탄성섬유를 장기적으로 안정하게 제조하는 방법을 제공하고자 한다.
The present invention significantly improves the dyeing and light resistance of polyurethaneurea elastic fibers by using a new type of additive, and at the same time prevents the process failure caused by the heat withdrawal of the additives during the spinning process. To provide a method for producing a stable as.

본 발명은 폴리우레탄우레아 중합체 용액을 방사하여 폴리우레탄우레아 탄성섬유를 제조함에 있어서, 상기 중합체 용액에 아래 일반식(Ⅰ)의 3급 아민을 포함하는 디에스테르 화합물을 첨가하는 것을 특징으로 한다.The present invention is to produce a polyurethane urea elastic fiber by spinning a polyurethane urea polymer solution, characterized in that the diester compound containing a tertiary amine of the general formula (I) below to the polymer solution.

- 아 래 -                          -Below-

Figure 112004061111693-pat00001
Figure 112004061111693-pat00001

(상기 식에서, R1 및 R2는 탄소수 1~10의 알킬이고, R3∼R6는 수소이거나 탄소수 1∼4의 선형 또는 가지형 알킬이다.)(Wherein R 1 and R 2 are alkyl having 1 to 10 carbon atoms, and R 3 to R 6 are hydrogen or linear or branched alkyl having 1 to 4 carbon atoms.)

또한 본 발명의 폴리우레탄우레아 탄성섬유는 일반식(Ⅰ)의 3급 아민을 포함하는 디에스테르 화합물을 0.1~3.0중량% 함유하여, 염색성을 나타내는 분배율이 5~97% 이고, 내광성을 나타내는 강력유지율이 60~97%인 것을 특징으로 한다.In addition, the polyurethaneurea elastic fiber of the present invention contains 0.1 to 3.0% by weight of a diester compound containing a tertiary amine of the general formula (I), and has a distribution ratio of 5 to 97%, which indicates dyeing resistance, and a strong retention rate indicating light resistance. It is characterized by the 60-97%.

이하, 본 발명을 상세하게 설명한다.EMBODIMENT OF THE INVENTION Hereinafter, this invention is demonstrated in detail.

본 발명은 먼저, 수평균 분자량 1500~2000의 고분자량 디올화합물 1몰에 대하여 디이소시아네이트 화합물 1.5~1.8몰을 예비중합한 후 용제를 적당량 혼합하여 예비중합물의 용액을 제조한 후, 디아민 화합물을 예비중합물의 70~99몰%, 모노아 민 화합물을 예비중합물의 1~30몰% 사용하여 예비중합물을 쇄연장 및 쇄정지를 동시에 시켜서 방사에 적당한 점도인 1500~5000포아즈(40℃)의 폴리우레탄우레아 중합체를 제조한다.First, the present invention first prepolymerizes 1.5 to 1.8 moles of the diisocyanate compound with respect to 1 mole of the high molecular weight diol compound having a number average molecular weight of 1500 to 2000, and then a suitable amount of the solvent is mixed to prepare a solution of the prepolymer, followed by preparing a diamine compound. 70-99 mol% of the polymer and 1-30 mol% of the monoamine compound are used to simultaneously extend the chain and stop the prepolymer so that the polypropylene of 1500-5000 poise (40 ° C.) is suitable for spinning. Urethane urea polymer is prepared.

상기의 디아민 화합물은 에틸렌디아민, 1,2-디아미노프로판 또는 2-메틸-1,5-펜타메틸렌디아민이 각각 적용될 수도 있고, 에틸렌디아민과 1,2-디아미노프로판이 혼합된 형태나 에틸렌디아민과 2-메틸-1,5-펜타메틸렌디아민이 혼합된 형태로 적용될 수도 있다. 상기의 모노아민은 디에틸아민이 주로 사용된다.Ethylenediamine, 1,2-diaminopropane or 2-methyl-1,5-pentamethylenediamine may be applied to the diamine compound, or a mixture of ethylenediamine and 1,2-diaminopropane or ethylenediamine And 2-methyl-1,5-pentamethylenediamine may be applied in a mixed form. As the monoamine, diethylamine is mainly used.

다음으로 상기와 같이 제조된 폴리우레탄우레아 중합체에 상기 일반식(I)의 3급 아민을 포함하는 디에스테르 화합물을 첨가한다. 이들 화합물과 함께 통상의 입체장애된 페놀계 산화방지제 및 폐가스안정제를 첨가하는 것이 더욱 바람직 하다. 아울러 공지의 첨가제인 루틸(Rutile)형태의 산화티탄, 청색안료, 마그네슘스테아레이드 등도 첨가하는 것이 더욱 바람직 하다.Next, the diester compound containing the tertiary amine of the general formula (I) is added to the polyurethaneurea polymer prepared as described above. It is more preferred to add conventional hindered phenolic antioxidants and waste gas stabilizers with these compounds. In addition, it is more preferable to add a known type of rutile (Rutile) titanium oxide, blue pigment, magnesium stearate and the like.

본 발명에 있어서 상기 일반식(Ⅰ)의 3급 아민을 포함하는 디에스테르 화합물의 투입량은 중합체 고형분 대비 각각 0.1~3.0중량%로 하는 것이 바람직 하다. 만약 상기 화합물의 투입량이 0.1중량% 미만인 경우에는 탄성섬유의 내광성 및 염색성 개선효과가 저하될 수 있고, 3.0중량%를 초과하는 경우에는 방사성에 악영향을 미칠 수 있다.In the present invention, the amount of the diester compound containing the tertiary amine of the general formula (I) is preferably 0.1 to 3.0% by weight relative to the polymer solid content. If the amount of the compound is less than 0.1% by weight, the effect of improving the light resistance and dyeing property of the elastic fiber may be lowered, and if it exceeds 3.0% by weight, it may adversely affect radioactivity.

본 발명에서는 상기 일반식(I)의 화합물을 통상의 산화방지제, 폐가스안정제, 마그네슘스테아레이트, 산화티탄 및/또는 청색안료 등과 동시에 폴리우레탄우레아 중합체에 투입하여도 무방하다. In the present invention, the compound of general formula (I) may be added to the polyurethane urea polymer simultaneously with a conventional antioxidant, waste gas stabilizer, magnesium stearate, titanium oxide and / or blue pigment.

이때 산화방지제로는 입체장애된 페놀계 산화방지제를 폐가스안정제로는 세미카바지이드계 폐가스안정제를 청색안료로는 울트라마린블루를 사용 할수 있다. 또한 산화티탄으로는 루틸형태의 산화티탄을 사용하는 것이 좋다.In this case, a sterically hindered phenolic antioxidant may be used as an antioxidant, a semicarbazide-based waste gas stabilizer as a waste gas stabilizer, and ultramarine blue may be used as a blue pigment. As the titanium oxide, rutile titanium oxide is preferably used.

예를 들면, 입체장애된 페놀계 산화방지제 0.1~1.5중량%, 세미카바지이드계 폐가스안정제 0.1~2.0중량%, 투틸형태의 산화티탄 0.05~4.0중량%, 마그네슘스테아레이트 0.1~0.5중량% 및 청색안료 0.005~0.02중량%를 상기 일반식(I)의 화합물과 함께 폴리우레탄우레아 중합체에 투입 할 수 있다.For example, 0.1-1.5% by weight of sterically hindered phenolic antioxidants, 0.1-2.0% by weight of semicarbazide-based waste gas stabilizers, 0.05-4.0% by weight of titanium oxide in tutyl form, 0.1-0.5% by weight of magnesium stearate and blue 0.005 to 0.02% by weight of the pigment may be added to the polyurethaneurea polymer together with the compound of formula (I).

본 발명은 다음으로 상기와 같이 첨가제 조성물이 첨가 완료된 폴리우레탄우레아 중합체를 통상의 방법으로 건식 또는 습식 방사하여 본 발명의 폴리우레탄우레아 탄성섬유를 제조한다.The present invention is to produce a polyurethane urea elastic fiber of the present invention by dry or wet spinning the polyurethane urea polymer is added to the additive composition as described above in a conventional manner.

본 발명에서는 내열성이 우수한 상기 일반식(Ⅰ)의 디에스테르 화합물을 첨가하기 때문에 첨가량을 적게하여도 내광성이 매우 우수하다. 그 결과 고온의 방사공정 중 첨가제가 열에 의해 취화되어 방사공정에 악영향을 미치는 현상을 효과적으로 방지 할 수 있다. 또한 일반식(Ⅰ)의 3급 아민을 포함하는 디에스테르 화합물이 내열제 역할과 동시에 염색증진제 역할도 수행하기 때문에 별도의 염색증진제를 사용하지 않아도 섬유의 염색성이 향상된다.In this invention, since the diester compound of the said general formula (I) which is excellent in heat resistance is added, even if the addition amount is small, it is very excellent in light resistance. As a result, it is possible to effectively prevent the phenomenon that the additive is embrittled by heat during the high-temperature spinning process adversely affects the spinning process. In addition, since the diester compound including the tertiary amine of the general formula (I) plays a role of a heat enhancer and a dye enhancer, dyeing of fibers is improved without using a separate dye enhancer.

본 발명의 탄성섬유는 염색성을 나타내는 분배율이 5~97% 이고, 내광성을 나타내는 강력유지율이 60~97% 이다.The elastic fiber of the present invention has a distribution ratio of 5 to 97% showing dyeing property, and a strong retention rate of 60 to 97% showing light resistance.

본 발명에 있어서, 염색성과 내광성은 아래 방법으로 평가한다.In the present invention, dyeability and light resistance are evaluated by the following method.

·내광성Light resistance

내광성은 강력유지율과 황변지수(Yellowness Index : △b)로 표시 하였다.Light resistance was expressed by strong retention and yellowness index (Δb).

(ⅰ) 황변지수(△b) : 40데니어의 폴리우레탄우레아 탄성섬유를 알루미늄판에 감아 웨드-오-메타에서 선샤인카본아크로 24시간 처리후 측정 한다.(Iii) Yellowness index (△ b): 40 denier polyurethane urea elastic fibers are wound on an aluminum sheet and measured after 24 hours treatment with sunshine carbon arc in a wet-o-meta.

(ⅱ) 강력유지율(%): 웨드-오-메타에서 자외선을 조광하기 전·후의 탄성섬유 강력을 인스트롱에서 측정(시료길이 5cm, 속도 50cm/분)하여 다음식에 대입하여 구한다.(Ii) Strength retention rate (%): The strength of elastic fibers before and after dimming ultraviolet rays in the WED-O-MET is measured by instron (sample length 5cm, speed 50cm / min) and substituted by the following formula.

Figure 112004061111693-pat00002
Figure 112004061111693-pat00002

·염색성Dyeing

염색성은 아래 단계를 거쳐 평가되는 분배율로 표시한다.Dyeability is expressed by the partition ratio evaluated through the following steps.

(ⅰ) 튜브-니터(Tube-Knitter)를 사용하여 2합으로 나일론 환편지와 폴리우레탄우레아 탄성섬유 환편지를 각각 제편한 다음 이들을 아래 조건하에서 정련 및 염색한다.(Iii) Using a tube-knitter, nylon circular knits and polyurethaneurea elastic fiber circular knits are knitted in two batches, and they are refined and dyed under the following conditions.

<정련조건> : Na2CO3 3g/ℓ 및 세제 1g/ℓ의 조성을 갖는 정련욕(욕비:1/30)을 사용하여 마티스(MATIS) 염색기에서 80℃×30분 동안 정련한다.<Refining conditions>: Refining was carried out in a Matis dyeing machine using a refining bath (bath ratio: 1/30) having a composition of 3 g / l Na 2 CO 3 and 1 g / l detergent for 80 ° C. × 30 minutes.

<염색조건> : 산성염료(Nylosan Red N-2RBL) 0.5% owf 염액으로 40℃에서 60분 동안 염색하고, 계속해서 1℃/분의 감온속도로 80℃까지 온도를 내리면서 염색을 완료 한다.<Dyeing condition>: Dyeing with acid dye (Nylosan Red N-2RBL) 0.5% owf saline at 40 ° C for 60 minutes, then complete the dyeing while lowering the temperature to 80 ° C at a temperature reduction rate of 1 ° C / min.

(ⅱ) 상기와 같이 염색된 나일론 환편지와 폴리우레탄우레아 탄성섬유 환편지의 반사율을 분광광도계로 측정한 후 최대 흡수 파장에서 각각의 K/S를 측정한다.(Ii) The reflectances of the nylon circular knitted fabrics and the polyurethaneurea elastic fiber circular knitted fabrics dyed as described above were measured with a spectrophotometer, and each K / S was measured at the maximum absorption wavelength.

Figure 112004061111693-pat00003
Figure 112004061111693-pat00003

여기서 R은 반사율이고, K는 흡광계수이고, S는 산란계수 이다.        Where R is the reflectance, K is the extinction coefficient, and S is the scattering coefficient.

(ⅲ) 상기에서 측정된 각각의 K/S 값을 아래식에 대입하여 분배율(%)을 구한다.(Iv) Substituting the K / S values measured above into the following equation, calculate the distribution ratio (%).

Figure 112004061111693-pat00004
Figure 112004061111693-pat00004

이하 실시예 및 비교실시예를 통하여 본 발명을 더욱 구체적으로 살펴본다. 그러나 본 발명은 하기 실시예에만 한정되는 것은 아니다.Hereinafter, the present invention will be described in more detail with reference to Examples and Comparative Examples. However, the present invention is not limited only to the following examples.

실시예 1Example 1

분자량 1800의 폴리테트라메틸렌글리콜 1몰에 4,4'-디페닐메탄디이소시아네이트 1.7몰을 혼합하여 90℃에서 90분간 반응시켜 양말단에 이소시아네이트를 갖는 프리폴리머를 합성 하였다. 이 프리폴리머를 40℃로 냉각시킨 후 N,N'-디메틸아세트아마이드를 첨가하여 약 45%의 프리폴리머를 포함하는 용액을 제조 하였다. 이 프리폴리머 용액을 5℃까지 낮춘 후 격렬히 교반하면서 프리폴리머에 대하여 에틸렌디아민을 96당량%, 디에틸아민 6당량%를 함유한 N,N'-디메틸아세트아마이드 용액을 천천히 가하면서 쇄연장 및 쇄중지를 시켜 최종적인 폴리우레탄우레아 용액을 제조 하였다. 얻어진 폴리우레탄우레아 용액에 1,3,5-트리스(4-t-부틸-3-하이드록시-2,6-디메틸벤젠)-1,3,5-트리아진-2,4,6-(1H,3H,5H)트라이온 산화방지제를 폴리우레탄우레아 용액의 고형분 대비 1.0중량%, 하기 일반식(Ⅱ)의 구조를 갖는 3급아민을 포함하는 디에스테르 화합물 2.5중량%(폴리우레탄우레아 용액 고형분 대비), 산화티탄 0.5중량%, 청색안료(울트라마린블루) 0.01중량%를 첨가하여 220℃ 분위기에서 방사하여 40데니어의 폴리우레탄우레아 탄성섬유를 제조 하였다. 제조된 탄성섬유의 내광성 및 염색성을 평가한 결과는 표 2와 같다.1.7 moles of 4,4′-diphenylmethane diisocyanate was mixed with 1 mole of polytetramethylene glycol having a molecular weight of 1800 and reacted at 90 ° C. for 90 minutes to synthesize a prepolymer having an isocyanate at the sock end. After cooling the prepolymer to 40 ° C., N, N′-dimethylacetamide was added to prepare a solution containing about 45% of the prepolymer. The prepolymer solution was lowered to 5 ° C., followed by vigorous stirring, while slowly adding a N, N'-dimethylacetamide solution containing 96 equivalents of ethylenediamine and 6 equivalents of diethylamine to the prepolymer, while slowly extending the chain and stopping the chain. The final polyurethaneurea solution was prepared. 1,3,5-tris (4-t-butyl-3-hydroxy-2,6-dimethylbenzene) -1,3,5-triazine-2,4,6- (1H in the obtained polyurethaneurea solution 2.5 wt% of a (3H, 5H) trione antioxidant, based on the solid content of the polyurethaneurea solution, of a diester compound containing a tertiary amine having a structure of the following general formula (II) (2.5% by weight of the polyurethaneurea solution solids) ), 0.5% by weight of titanium oxide, 0.01% by weight of blue pigment (ultramarine blue) was added to spin in an atmosphere of 220 ℃ to prepare a polyurethane denier polyurethane urea of 40 denier. The results of evaluating the light resistance and dyeability of the prepared elastic fibers are shown in Table 2.

Figure 112004061111693-pat00005
Figure 112004061111693-pat00005

실시예 2 및 비교실시예 1Example 2 and Comparative Example 1

폴리우레탄 용액의 고형분 대비 상기 일반식(Ⅱ)의 구조를 갖는 3급 아민을 포함하는 디에스테르 화합물 (이하 "Y 화합물"이라고 한다)의 투입량을 표 1과 같이 변경한 것을 제외하고는 실시예 1과 동일한 공정으로 40데니어의 폴리우레탄우레아 탄성섬유를 제조 하였다. 제조된 탄성섬유의 내광성 및 염색성을 평가한 결과 는 표 2와 같다.Example 1 except that the amount of the diester compound (hereinafter referred to as "Y compound") containing the tertiary amine having the structure of Formula (II) relative to the solid content of the polyurethane solution was changed as shown in Table 1 Polyurethane urea elastic fiber of 40 denier was prepared in the same process. The results of evaluating the light resistance and dyeability of the prepared elastic fibers are shown in Table 2.

제조조건Manufacture conditions 구 분division 실시예 1Example 1 실시예 2Example 2 비교실시예 1Comparative Example 1 Y 화합물 투입량(중량%)Y compound dose (% by weight) 2.52.5 0.10.1 00

물성평가 결과Property evaluation result 구분division 내광성Light resistance 염색분배율(%)Dyeing percentage (%) △bΔb 강력유지율(%)Strong retention rate (%) 실시예 1Example 1 33 9696 9696 실시예 2Example 2 1010 7070 1010 실시예 3Example 3 3636 88 22

본 발명은 폴리우레탄우레아 탄성섬유의 염색성 및 내광성을 개선시킬 수 있으며, 방사공정의 조업성도 향상시킬 수 있다.The present invention can improve the dyeing and light resistance of the polyurethane urea elastic fiber, it can also improve the operation of the spinning process.

Claims (5)

폴리우레탄우레아 중합체 용액을 방사하여 폴리우레탄우레아 탄성섬유를 제조함에 있어서, 상기 중합체 용액에 아래 일반식(Ⅰ)의 3급 아민을 포함하는 디에스테르 화합물을 첨가하는 것을 특징으로 하는 염색성 및 내광성이 우수한 폴리우레탄우레아 탄성섬유의 제조방법.In spinning a polyurethane urea polymer solution to produce a polyurethane urea elastic fiber, it is excellent in dyeing and light resistance, characterized by adding a diester compound containing a tertiary amine of the general formula (I) Method for producing polyurethane urea elastic fiber. - 아 래 -                           -Below-
Figure 112004061111693-pat00006
Figure 112004061111693-pat00006
(상기 식에서, R1 및 R2는 탄소수 1~10의 알킬이고, R3∼R6는 수소이거나 탄소수 1∼4의 선형 또는 가지형 알킬이다.)(Wherein R 1 and R 2 are alkyl having 1 to 10 carbon atoms, and R 3 to R 6 are hydrogen or linear or branched alkyl having 1 to 4 carbon atoms.)
1항에 있어서, 일반식(Ⅰ)의 3급 아민을 포함하는 디에스테르 화합물을 폴리우레탄우레아 중합체 고형분 대비 0.01~3.0중량% 첨가하는 것을 특징으로 하는 염색성 및 내광성이 우수한 폴리우레탄우레아 탄성섬유의 제조방법.A polyurethane urea elastic fiber having excellent dyeing and light resistance according to claim 1, wherein a diester compound comprising a tertiary amine of the general formula (I) is added in an amount of 0.01 to 3.0% by weight based on the polyurethane urea polymer solid content. Way. 아래 일반식(Ⅰ)의 3급 아민을 포함하는 디에스테르 화합물을 0.1~3.0중량% 함유하는 것을 특징으로 하는 염색성 및 내광성이 우수한 폴리우레탄우레아 탄성섬유.Polyurethane urea elastic fiber excellent in dyeing properties and light resistance, characterized by containing 0.1 to 3.0% by weight of a diester compound containing a tertiary amine of the general formula (I) below. - 아 래 -                          -Below-
Figure 112004061111693-pat00007
Figure 112004061111693-pat00007
(상기 식에서, R1 및 R2는 탄소수 1~10의 알킬이고, R3∼R6는 수소이거나 탄소수 1∼4의 선형 또는 가지형 알킬이다.)(Wherein R 1 and R 2 are alkyl having 1 to 10 carbon atoms, and R 3 to R 6 are hydrogen or linear or branched alkyl having 1 to 4 carbon atoms.)
3항에 있어서, 염색성을 나타내는 분배율이 5~97% 인 것을 특징으로 하는 염색성 및 내광성이 우수한 폴리우레탄우레아 탄성섬유. The polyurethaneurea elastic fiber excellent in dyeing property and light resistance of Claim 3 whose distribution ratio which shows dyeing property is 5 to 97%. 3항에 있어서, 폴리우레탄우레아 탄성섬유의 강력유지율이 60~97% 인 것을 특징으로 하는 염색성 및 내광성이 우수한 폴리우레탄우레아 탄성섬유.The polyurethane urea elastic fiber having excellent dyeing and light resistance according to claim 3, wherein the polyurethane urea elastic fiber has a strong retention of 60 to 97%.
KR1020040111713A 2004-12-24 2004-12-24 A polyurethaneurea elastic fiber with excellent dyeing property and light resistance, and a process of preparing the same KR100580325B1 (en)

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KR20030029167A (en) * 2001-10-05 2003-04-14 주식회사 코오롱 A polyurethaneurea elastic fiber with excellent light resistance and dyeing property, and a process of preparing the same

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