KR20030000760A - Carrier dyeing method for PTT fiber by using the natural terpene and PTT fiber poduced by the said method - Google Patents

Carrier dyeing method for PTT fiber by using the natural terpene and PTT fiber poduced by the said method Download PDF

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KR20030000760A
KR20030000760A KR1020010036876A KR20010036876A KR20030000760A KR 20030000760 A KR20030000760 A KR 20030000760A KR 1020010036876 A KR1020010036876 A KR 1020010036876A KR 20010036876 A KR20010036876 A KR 20010036876A KR 20030000760 A KR20030000760 A KR 20030000760A
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ptt
dyeing
carrier
terpene
fiber
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KR100419524B1 (en
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송기철
유제안
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주식회사 효성
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    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P3/00Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
    • D06P3/004Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated using dispersed dyes
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/34General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using natural dyestuffs
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P3/00Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
    • D06P3/34Material containing ester groups
    • D06P3/36Material containing ester groups using dispersed dyestuffs

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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Coloring (AREA)

Abstract

PURPOSE: Provided are a dyeing method of polytrimethylene terephthalate(PTT) fiber using a carrier containing natural terpene which doesn't pollute environment, doesn't generate an offensive odor and harmful steam and is capable of dyeing deep color, and the polytrimethylene terephthalate fiber having good fastness. CONSTITUTION: The PTT fiber is dyed by using the carrier containing the natural terpene. Terpene has monoterpene structure or diterpene structure. Monoterpene has monocyclic structure or dicyclic structure. The carrier is mixed with an emulsifier, a dispersant and the terpene ingredient modified with water soluble derivatives. Dyeing conditions are as follows: using 1-20wt.% of the carrier based on the fiber; having 1:5-1:50 of bath ratio; and dyeing at 80-120deg.C for 20-80minutes.

Description

천연 테르펜 성분의 캐리어를 이용한 폴리트리메틸렌 테레프탈레이트 섬유의 염색방법 및 그 폴리트리메틸렌 테레프탈레이트 섬유{Carrier dyeing method for PTT fiber by using the natural terpene and PTT fiber poduced by the said method}Carrier dyeing method for PTT fiber by using the natural terpene and PTT fiber poduced by the said method}

본 발명은 테르펜류의 캐리어(carrier)를 이용한 PTT(폴리트리메틸렌 테레프탈레이트)섬유의 저온염색 방법 및 그 PTT 섬유에 관한 것이다.The present invention relates to a low-temperature dyeing method of PTT (polytrimethylene terephthalate) fibers using a carrier of terpenes and the PTT fibers thereof.

캐리어는 과거에도 폴리에스테르섬유나 나일론 섬유의 저온염색, 얼룩방지, 정련 등의 가공에 사용되어져 왔다.Carriers have been used for low temperature dyeing, stain prevention, and refining of polyester and nylon fibers in the past.

특히 폴리에스테르 섬유와 타섬유와의 혼방품을 염색할 때 폴리에스테르의 염색온도인 130℃부근까지 온도를 올리게 되면 울, 실크 등의 타 섬유 성분을 취화시키기 때문에 이를 막기 위해 캐리어가 사용되어 왔다.In particular, when dyeing a blend of polyester fibers and other fibers, the carrier has been used to prevent other fiber components, such as wool and silk, when the temperature is raised to around 130 ° C, which is a dyeing temperature of the polyester.

다시 말하면 고온에서 쉽게 취화되는 단백질섬유나 셀룰로우스 섬유 성분의 취화를 막기 위해 100 ∼ 105℃에서 염색을 하게되면, 폴리에스테르 섬유의 농염을 얻기가 힘들기 때문에 캐리어를 사용하여 농염을 얻는 방법이 사용되어 왔다.In other words, in order to prevent embrittlement of protein fibers or cellulose fibers that are easily embrittled at high temperatures, dyeing at 100 to 105 ° C. makes it difficult to obtain concentrated salts of polyester fibers. Has been used.

최근에 PET섬유보다 우수한 방오성, 신도, 염색성 등의 성질을 가진 PTT섬유가 개발되었으나, 이러한 PTT섬유는 100℃이하의 온도에서는 농색을 얻기에 충분하지 못한 염착량을 나타내기 때문에 충분한 색농도를 나타내기 위해서는 캐리어의 사용이 불가피하다.In recent years, PTT fibers with superior antifouling properties, elongation, and dyeing properties have been developed, but these PTT fibers exhibit sufficient color concentrations due to their insufficient dyeing at 100 ° C or below. In order to bet, use of a carrier is inevitable.

그러나 종래의 캐리어는 페닐페놀, 디페닐, 메틸나프탈렌, 디클롤벤젠, 트리클롤벤젠 등을 주성분으로 하고 있고 이러한 화합물은 인체에 유해한 물질이고 작업시 악취를 발생시키며 환경오염 등의 문제점을 가지고 있어 실제로 사용이 기피되고 있는 실정이다.However, the conventional carrier is mainly composed of phenylphenol, diphenyl, methylnaphthalene, dichlorobenzene, trichlorobenzene and the like, and these compounds are harmful to the human body, cause odor during work, and have environmental problems such as environmental pollution. Use is being avoided.

본 발명은 환경에 대한 오염이 적고, 악취발생이 없으며, 저온에서의 농염염색이 가능한 종래의 캐리어를 대신하는 천연 테르펜 성분의 캐리어 를 이용한 PTT섬유의 염법 및 그 PTT섬유 염색물을 제공하는 것을 목적으로 한다.An object of the present invention is to provide a salt method of PTT fiber and a dyeing method of PTT fiber using a carrier of a natural terpene component instead of the conventional carrier which is less polluted to the environment, has no odor, and is capable of thick dyeing at low temperatures. It is done.

본 발명자들은 상기 과제를 해결하기 위해 환경오염이 적고 악취가 없으며 인체에 악영향이 없을 것으로 생각되는 여러 가지의 천연유래의 물질을 검토한 결과, 저분자의 천연식물유가 캐리어로서 유효하다는 것을 발견하고, 이러한 저분자 식물 정유(精油)의 주성분인 테르펜(terpene)이 캐리어로써 유효한 성분이라는 것을 밝혀내어 본 발명을 완성하게 되었다.In order to solve the above problems, the present inventors have studied various natural-derived substances that are considered to have little environmental pollution, no odor, and no adverse effects on the human body, and have found that low molecular weight natural vegetable oils are effective as carriers. The present invention has been completed by finding that terpene, which is a main component of low molecular weight plant essential oil, is an effective ingredient as a carrier.

천연물질에서 유래한 테르펜은 탄소 10개, 수소 16개(H10C16)의 조성을 갖는 화합물로서, 주로 소나무과 식물(소나무, 정향, 편백 등)의 정유에 많이 함유되어 있는 성분이다. 항균, 항염 효과가 뛰어나 많은 전문가들에 의해 연구되어 현재는400여 이상의 종류가 규명되었으며, 많이 알려진 항암제 탁솔도 테르펜의 알칼라이드 유도체이다.Terpenes derived from natural substances are compounds having a composition of 10 carbons and 16 hydrogens (H10C16), and are mainly contained in essential oils of pine trees (pine, clove, cypress, etc.). The antimicrobial and anti-inflammatory effects have been studied by many experts, and more than 400 types have been identified. The well-known anticancer drug Taxol is also an alkalide derivative of terpene.

그밖에 핀넨, 캄펜, 시네올, 펜콘, 보르네올, 아네톨, 다이멘(thymen), 카마주렌(chamazulene)등이 약품으로 상용화되어 있다.In addition, Pinnen, Campen, Cineol, Fencon, Borneol, Anetol, thymen, chamazulene, etc. are commercially available.

또한 테르펜은 비극성 악취분자와 화학적으로 반응하여 가스상태의 악취를 이온화시킴으로써 냄새를 제거하는 효과도 가지고 있으므로 테르펜으로 캐리어 염색하면 악취의 우려가 없다.In addition, terpenes have the effect of removing odors by chemically reacting with nonpolar malodorous molecules and ionizing gaseous malodors, so there is no fear of malodors when carrier-dyed with terpenes.

상기의 천연물질에서 유래한 테르펜 성분의 캐리어로서 모노싸이클릭(monocyclic) 구조를 갖는 메탄계(methane type)의 모노테르펜(monoterpene)류는 아래 화학식 1 ∼ 3과 같은 멘탄(menthane), 멘텐(menthene), 멘타디엔(menthadiene) 유도체의 형태를 가진다.Methane-type monoterpenes having a monocyclic structure as a carrier of the terpene component derived from the natural substance are menthane and menthene represented by Chemical Formulas 1 to 3 below. ) And the form of menthadiene derivatives.

(화학식 1) (화학식 2) (화학식 3) (Formula 1) (Formula 2) (Formula 3)

(m-멘탄) (1-p-멘텐) (1,4(8)-p-멘타디엔)(m-mentan) (1-p-mentene) (1,4 (8) -p-mentadiene)

상기의 모노싸이클릭(monocyclic) 구조를 갖는 메탄(methane)은 또 다른 형태로써 테트라메틸-싸이클로헥산 타이프(Tetramethyl-cyclohexane type)으로 분류되는 화학식 4 ∼ 6과 같은 형태의 싸이클로헥산(cyclohexane), 싸이클로헥센(cyclohexene) 그리고 싸이클로헥사디엔(cyclohexadiene) 유도체들로 구분된다.Methane (monocyclic) having a monocyclic structure is another form of the cyclohexane (cyclohexane) of the form of the formula (4-6), which is classified as tetramethyl-cyclohexane type (Tetramethyl-cyclohexane type) Hexane (cyclohexene) and cyclohexadiene derivatives.

(화학식 4) (화학식 5) (화학식 6)(Formula 4) (Formula 5) (Formula 6)

(1,1,2,3-테트라메틸 (1,2,3,3-테트라메틸- (1,5,5,6-테트라메틸(1,1,2,3-tetramethyl (1,2,3,3-tetramethyl- (1,5,5,6-tetramethyl)

싸이클로헥산) -싸이클로헥센) -13-싸이클로헥사디엔)Cyclohexane) -cyclohexene) -13-cyclohexadiene)

모노테르펜(monoterpene)이며 디싸이클릭(dicyclic) 구조의 테르펜은 다음 화학식 7 ∼ 11 과 같은 구조를 가지는 것을 특징으로 하는 화합물들이다.Monoterpenes (monoterpene) and dicyclic terpene terpene is a compound characterized by having the structure shown in the following formula (7).

(화학식 7) (화학식 8) (화학식 9)(Formula 7) (Formula 8) (Formula 9)

(2-카렌) (5-이소프로필 바이싸이클로 (7,7-디메틸-2,4-(2-karen) (5-isopropyl bicyclo (7,7-dimethyl-2,4-

(3,1,0)헥스-2-엔) 놀카라디엔)(3,1,0) hex-2-yen) nolvadiene)

(화학식 10) (화학식 11)Formula 10

(4(10)-두젠) (캄펜)(4 (10) -Dusen) (Kampen)

상기의 테르펜 중에서 디테르펜(diterpene) 및 싸이클릭디테르펜(cyclic diterpene)류는 2-메틸-1, 3-부타디엔(2-methyl-1, 3-butadiene)의 분자 4개가 결합된 형태이며 대표적인 물질로는 비타민A가 여기에 속한다.Among the terpenes, diterpenes and cyclic diterpenes are in the form of a combination of four molecules of 2-methyl-1, 3-butadiene (2-methyl-1, 3-butadiene). Vitamin A belongs to this.

상기의 모노테르펜과 디테르펜은 천연물의 추출물로써 발견된다.The monoterpenes and diterpenes are found as extracts of natural products.

천연물의 추출물의 예로는 페퍼민트유, 시나몬유, 스페어민트유, 레몬유, 유자오일, 라임오일, 그레이프프르츠오일, 샌들우드기름, 월계수기름, 송유, 생강유, 로즈마리오일 등이 있으며 여기서 테르펜을 추출할 수 있다.Examples of natural extracts include peppermint oil, cinnamon oil, sparemint oil, lemon oil, citron oil, lime oil, grapefruit oil, sandalwood oil, laurel oil, pine oil, ginger oil, rosemary oil, and the like. can do.

또 이러한 천연오일로부터 단일 성분으로 정제된 테르펜 성분으로는 S-, T-, D-리모넨(Limonene), α-파르네센(α-farnesene), β-셀리넨(β-selinene), 캄펜(camphene), 제라니올(geraniol), 멘톨(menthol), α-,β-핀넨(pinene), 테르핀올(Terpineol) 등이 알려져 있다.In addition, terpene components purified from natural oil as a single component include S-, T-, D-limonene, α-farnesene, α-farnesene, β-selinene, and camphene. ), Geraniol, germentol, menthol, α-, β-pinene, terpineol and the like are known.

또한 본 발명에서 사용하는 테르펜 성분은, 화학합성에 의해 합성된 구조적으로 동일한 화합물을 포함하는 것으로 한다.In addition, the terpene component used by this invention shall contain the structurally identical compound synthesize | combined by chemical synthesis.

상기의 테르펜은 친유성 물질이기 때문에, 친유성인 테르펜을 수용성으로 만들어주는 유도체로는 금속염의 형태로 변형한 것 또는 알코올 등의 형태로 개질한 유도체를 포함하며, 이는 물에서 염색할 때 캐리어의 용해성을 높이는 효과를 부여하는데 유용하다.Since the terpene is a lipophilic substance, derivatives that make the lipophilic terpenes water-soluble include derivatives modified in the form of metal salts or modified in the form of alcohols, and the like. It is useful for imparting an effect of increasing solubility.

테르펜을 수중에서 유화, 분산, 용해하기 위해 분산제, 유화제 등의 계면활성제를 혼합한 캐리어를 사용하며, 일반적인 계면 활성제로써 음이온성, 비이온성, 양쪽성 등 계면활성제의 종류에 관계없이 HLB의 범위가 9 ∼ 17 범위 내의 유화력을 가진 것을 사용하며, 10 ∼ 14의 범위의 것이 좋다.In order to emulsify, disperse, and dissolve terpene in water, a carrier mixed with a surfactant such as a dispersant and an emulsifier is used. The thing which has an emulsification power in the range of 9-17 is used, and the thing of the range of 10-14 is good.

상기의 캐리어를 사용하는 염색방법은 원료염, 사염, 포염 등을 모두 포함하는 형태의 염법에서 적용이 가능하며, 배치식 염색이나 연속염색, 나염, 젯트 프린팅 등의 방법에 관계없이 PTT를 분산염료로 염색하는 모든 방법을 포함한다.The dyeing method using the carrier can be applied in the salt method including all raw salts, salts, and flames, and disperse the PTT regardless of the method of batch dyeing, continuous dyeing, printing, jet printing, or the like. Including all methods to dye.

특히 피염물과 열매체와의 접촉시간이 배치염색에 비해 적은 연속염색 및 나염 등의 방법에서 더욱 효과적이다.In particular, the contact time between the chlorine and the heat medium is more effective in the continuous dyeing and printing method than the batch dyeing.

본 발명의 캐리어를 이용하여 염색할 수 있는 PTT섬유로서는 PTT 100% 뿐만 아니라, PTT/나이론, PTT/면, PTT/모, PTT/PET등 PTT섬유와 타 섬유와의 복합섬유도 포함되며, 또한 실, 직물, 편물, 카페트, 부직포 등의 다양한 조직의 소재에 사용할 수 있다.PTT fibers that can be dyed using the carrier of the present invention include not only PTT 100%, but also composite fibers of PTT fibers such as PTT / nylon, PTT / cotton, PTT / hair, PTT / PET and other fibers, and also It can be used for various tissue materials such as yarn, woven fabric, knitted fabric, carpet, and nonwoven fabric.

또한 PTT원사의 불투명성을 높이기 위해 사용한 이산화티탄(TiO2)를 포함한 PTT섬유도 여기에 포함된다.Also included are PTT fibers containing titanium dioxide (TiO 2 ) used to increase the opacity of PTT yarns.

이산화티탄을 사용하는 목적은 제품의 광택을 줄이기 위하여 사용하는데 통상 0.1 ∼ 2.0 중량% 범위의 이산화티탄을 함유한 것을 사용한다.The purpose of using titanium dioxide is to reduce the glossiness of the product, and usually contains a titanium dioxide in the range of 0.1 to 2.0% by weight.

본 발명의 캐리어를 사용하는 염색방법을 설명하면, 피염색 섬유에 대하여 1 ∼ 20중량%, 바람직한 것은 2 ∼ 8중량% 가 되도록 염욕에 첨가하여 사용된다.When the dyeing method using the carrier of this invention is demonstrated, it adds to a salt bath so that it may be 1 to 20 weight% with respect to a to-dyed fiber, and 2 to 8 weight% is preferable.

미리 캐리어욕 중에서 피염물을 처리한 후에 염색을 할 수 도 있다.It may be dyed after treating the salts in a carrier bath in advance.

PTT섬유를 염색하기 위하여 사용하는 염료는 분산염료이며 본 발명에서 추구하는 저온염색의 경우 저에너지 타입의 분산염료를 사용하는 것이 좋다.The dye used to dye the PTT fiber is a disperse dye, and in the case of low temperature dyeing pursued by the present invention, it is preferable to use a disperse dye of low energy type.

복합섬유인 경우에는 각각의 섬유에 적합한 염료를 사용하는 것이(예를 들면 나일론은 산성염료, 면은 직접 또는 반응염료 등) 가능하다.In the case of a composite fiber, it is possible to use a dye suitable for each fiber (for example, nylon is an acid dye, cotton is directly or a reaction dye, etc.).

PTT섬유를 염색할 때 분산성 및 균염성을 향상시키기 위해서 사용하는 분산제 또는 균염제를 사용하는 것도 가능하다.When dyeing PTT fibers, it is also possible to use a dispersing or leveling agent used to improve dispersibility and leveling properties.

이때 사용량은 0.5 ∼ 3.0 g/l의 양을 염색욕에 첨가하며, 염색의 욕비는 일반적으로 1:5 ∼ 1:50의 사이에서 행해지며, 연속 염색의 경우에는 염색욕에 피염물의 염액 보유량을 늘리기 위해 폴리아크릴산, 셀룰로우스 유도체, 알긴산 유도체, 변성 스타치 등을 사용한다.In this case, the amount of 0.5 to 3.0 g / l is added to the dyeing bath, and the bathing ratio of dyeing is generally performed between 1: 5 to 1:50. To increase polyacrylic acid, cellulose derivatives, alginic acid derivatives, modified starches and the like are used.

이때 염액의 피염물에 대한 픽업(pick-up)율은 일반적으로 100 ∼800% 이며, 일반적인 카페트의 연속 염색시에 이 비율은 300 ∼ 500% 가 된다.At this time, the pick-up rate of the salt solution to the salt solution is generally 100 to 800%, and this ratio is 300 to 500% during continuous dyeing of general carpets.

염색온도는 80 ∼ 120℃에서 가능하며 바람직한 것은 98 ∼ 103℃이고 염색시간은 담색의 경우에는 20 ∼ 40분, 중색의 경우에는 40 ∼ 60분, 농색의 경우에는 60 ∼ 80분으로 하여 충분한 레벨링과 견뢰도를 얻도록 한다.Dyeing temperature is possible at 80-120 ℃, preferred is 98-103 ℃, and dyeing time is 20-40 minutes for light color, 40-60 minutes for medium color, 60-80 minutes for deep color. And fastness.

PTT는 종래의 폴리에스테르섬유보다 유리전이온도가 낮기 때문에 위와 같은조건에서 충분한 농염이 가능하며 본 발명의 캐리어를 사용한 경우 80 ∼ 95℃에서도 충분한 농색의 발현이 가능하다.Since PTT has a lower glass transition temperature than the conventional polyester fiber, sufficient thick salt is possible under the above conditions, and when the carrier of the present invention is used, sufficient deep color expression is possible even at 80 to 95 ° C.

실시예 1Example 1

모노테르펜인 디-리모넨(D-limonene)을 캐리어로 사용하기 위하여 다음의 조성에 의하여 캐리어를 제조하였다.In order to use the monoterpene di-limonene (D-limonene) as a carrier, a carrier was prepared by the following composition.

디-리모넨 90 중량 %에 소디움 도데실 설포네이트(sodium dodecyl sulfonate)를 3중량%, 디스퍼소겐 피엔(Dispersogen PN) (Clariant 사.) 3중량%, 일가솔 피엘(irgasol PL) (ciba 사 제품)4중량% 혼합하여 캐리어를 제조하였다.90% by weight of di-limonene, 3% by weight of sodium dodecyl sulfonate, 3% by weight of Dispersogen PN (Clariant.), Irgasol PL (manufactured by ciba) 4% by weight of a carrier was prepared.

실시예 2Example 2

실시예 1의 디-리모넨을 캄펜(camphene)으로 대신한 이외에는 실시예 1과 똑같이 하여 캐리어를 제조하였다.A carrier was prepared in the same manner as in Example 1 except that the di-limonene of Example 1 was replaced with camphene.

실시예 3Example 3

실시예 1의 디-리모넨을 제라니올(geraniol)으로 대신한 이외에는 실시예 1과 똑같이 하여 캐리어를 제조하였다.A carrier was prepared in the same manner as in Example 1 except for replacing the di-limonene of Example 1 with geraniol.

실시예 4Example 4

실시예 1의 디-리모넨을 피넨(pinene)으로 대신한 이외에는 실시예 1과 똑같이 하여 캐리어를 제조하였다.A carrier was prepared in the same manner as in Example 1 except that the di-limonene of Example 1 was replaced with pinene.

비교예 1Comparative Example 1

실시예 1의 디-리모넨을 파라-클로로벤젠으로 대신한 이외에는 실시예 1과 똑같이 하여 캐리어를 제조하였다.A carrier was prepared in the same manner as in Example 1 except for replacing the di-limonene of Example 1 with para-chlorobenzene.

비교예 2Comparative Example 2

실시예 1의 디-리모넨을 오르토-페닐페놀로 대신한 이외에는 실시예 1과 똑같이 하여 캐리어를 제조하였다.A carrier was prepared in the same manner as in Example 1 except for replacing the di-limonene of Example 1 with ortho-phenylphenol.

비교예 3Comparative Example 3

실시예 1의 디-리모넨을 메틸나프탈렌으로 대신한 이외에는 실시예 1과 똑같이 하여 캐리어를 제조하였다.A carrier was prepared in the same manner as in Example 1 except that the di-limonene of Example 1 was replaced with methylnaphthalene.

비교예 4Comparative Example 4

아래의 실시예 5의 방법으로 캐리어를 넣지 않고 염색하였다.It stained without the carrier by the method of Example 5 below.

실시예 5Example 5

실시예 1 ∼ 4 및 비교예 1 ∼ 3의 캐리어를 이용하여, 폴리프로필렌 기포지에 PTT BCF를 기모하여 만든 카페트 백단을 사용하여 표 1과 같은 조건에서 염색하였다.Using the carriers of Examples 1 to 4 and Comparative Examples 1 to 3, it was dyed under the conditions shown in Table 1 using a carpet sandalwood made by raising PTT BCF on polypropylene foam paper.

< 표 1 > 염색조건<Table 1> Dyeing Condition

조건Condition 사용조제 또는 방법Preparation or method of use 사용농도Concentration 분산염료Disperse Dyes 포론 블랙(Foron Black) RD-SE 300Foron Black RD-SE 300 5% owf5% owf 캐리어carrier 실시예 1-4, 비교예 1-3의 캐리어Carriers of Examples 1-4 and Comparative Examples 1-3 5% owf5% owf 균염제Leveling agent Avosperse D (Avocet Chemicals 사)Avosperse D (Avocet Chemicals) 1g/l1 g / l 욕비Bathrobe 1:201:20 pHpH 6.0 (초산으로 조정)6.0 (adjusted to acetic acid) 승온시간Temperature rise time 1℃ /분1 ℃ / min 염색온도Dyeing temperature 100℃ × 30분100 ℃ × 30 minutes

< 농염효과의 평가 ><Evaluation of the pesticide effect>

실시예 5의 결과로 얻어진 염색물을 맥베쓰(macbeth)사의 coloreye-7000 스펙트로포토메터를 사용하여 K/S를 측정하였다.The resulting dye of Example 5 was measured for K / S using a Macbeth coloreye-7000 spectrophotometer.

비교예 4의 K/S값을 100으로 하고 이것에 대한 K/S값의 상대 비교치를 표 2 에 나타내었다.The K / S value of the comparative example 4 was set to 100, and the relative comparison value of the K / S value with respect to this is shown in Table 2.

또한 KS K0430방법에 의해 습윤 견뢰도를 비교하였다.In addition, the wet fastness was compared by the KS K0430 method.

< 표 2 ><Table 2>

캐리어의 종류Type of carrier K/S 값K / S value 견뢰도Color fastness 실시예 1Example 1 디-리모넨Di-limonene 124124 4-5급4-5 class 실시예 2Example 2 캄펜Kampen 112112 4급Grade 4 실시예 3Example 3 제라니올Geraniol 105105 4급Grade 4 실시예 4Example 4 피넨Pinene 121121 4급Grade 4 비교예 1Comparative Example 1 파라-클로로벤젠Para-chlorobenzene 130130 4급Grade 4 비교예 2Comparative Example 2 오르토-페닐페놀Ortho-phenylphenol 127127 4급Grade 4 비교예 3Comparative Example 3 메틸나프탈렌Methylnaphthalene 139139 4-5급4-5 class 비교예 4Comparative Example 4 없음none 100100 4-5급4-5 class

위 표 2의 결과로부터 알 수 있는 바와 같이 천연유래의 캐리어를 사용하여 PTT카페트를 상압 하에서 저온(100℃)에서 염색하는 경우에 환경오염이 적고 건강에 악영향을 미치는 증기 및 악취를 발생시키지 않으며 고온고압 또는 일반캐리어의 존재 하에서 상온에서 염색했을 경우에 얻을 수 있는 수준의 농색염색이 가능하며, 특히 디-리모넨을 케리어로 사용했을 경우 일반 캐리어를 사용한 경우와 거의 같은 수준의 농색을 얻을 수 있으며 견뢰도에도 아무런 영향을 끼치지 않음을 알 수 있다.As can be seen from the results of Table 2, when the PTT carpet is dyed at a low temperature (100 ° C.) under a normal pressure using a carrier derived from natural environment, there is little environmental pollution and does not generate steam and odor that adversely affects health, and high temperature. It is possible to achieve the deep color staining that can be obtained when dyeing at room temperature in the presence of a high pressure or a general carrier. Especially, when di-limonene is used as a carrier, the color can be almost the same as that of a general carrier. It can be seen that it does not affect anything.

본 발명은 환경오염이 적고 인체에 무해하며 악취발생이 적은 캐리어염색을 가능하게 할 뿐만 아니라 종래의 합성캐리어와 비교하여도 견뢰도 및 농염효과에손색이 없는 염색을 가능하게 한다.The present invention not only enables carrier staining, which is less harmful to the environment, harmless to the human body, and less likely to cause odor, but also enables dyeing without any damage to the fastness and thickening effect in comparison with conventional synthetic carriers.

Claims (6)

천연 테르펜(terpene)을 포함하고 있는 캐리어(carrier)를 이용함을 특징으로 하는 PTT(폴리트리메틸렌 테레프탈레이트)섬유의 염색방법.A method of dyeing PTT (polytrimethylene terephthalate) fibers, characterized in that using a carrier containing a natural terpene (terpene). 천연 테르펜(terpene)을 포함하고 있는 캐리어(carrier)를 이용하여 염색한 것을 특징으로 하는 PTT(폴리트리메틸렌 테레프탈레이트)섬유.PTT (polytrimethylene terephthalate) fiber, characterized in that the dye using a carrier containing a natural terpene (terpene). 제 1 항에 있어서, 테르펜은 모노테르펜(monoterpene) 또는 디테르펜(diterpene) 구조를 갖는 것임을 특징으로 하는 PTT(폴리트리메틸렌 테레프탈레이트)섬유의 염색방법.The method of claim 1, wherein the terpene has a monoterpene (monoterpene) or diterpene (diterpene) structure, characterized in that the dyeing method of PTT (polytrimethylene terephthalate) fibers. 제 3 항에 있어서, 모노테르펜은 모노싸이클릭(monocyclic) 또는 디싸이클릭(dicyclic) 구조를 갖는 것임을 특징으로 하는 PTT(폴리트리메틸렌 테레프탈레이트)섬유의 염색방법.4. The method for dyeing PTT (polytrimethylene terephthalate) fibers according to claim 3, wherein the monoterpene has a monocyclic or dicyclic structure. 제 1 항에 있어서, 캐리어는 수용성 유도체로 개질한 테르펜성분에 유화제와 분산제를 혼합시킨 것임을 특징으로 하는 PTT(폴리트리메틸렌 테레프탈레이트)섬유의 염색방법.The method for dyeing a PTT (polytrimethylene terephthalate) fiber according to claim 1, wherein the carrier is a mixture of an emulsifier and a dispersant in a terpene component modified with a water-soluble derivative. 제 2 항에 있어서, PTT섬유는 타섬유와의 혼방품 또는 타섬유와의 복합섬유로서 실, 직물, 편물, 카페트, 부직포 중에서 선택한 것임을 특징으로 하는 PTT(폴리트리메틸렌 테레프탈레이트)섬유.The PTT (polytrimethylene terephthalate) fiber according to claim 2, wherein the PTT fiber is selected from yarn, woven fabric, knitted fabric, carpet, and nonwoven fabric as a blended product with other fibers or a composite fiber with other fibers.
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KR100431784B1 (en) * 2001-11-01 2004-05-17 주식회사 효성 A method for dyeing PTT carpet continuously
CN113767253A (en) * 2019-04-22 2021-12-07 宋基喆 Floor block set

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JP4191317B2 (en) * 1999-05-18 2008-12-03 住江織物株式会社 Insect repellent composition for backing layer of fabrics such as carpet and fabrics such as carpet having insect repellent function
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KR100431784B1 (en) * 2001-11-01 2004-05-17 주식회사 효성 A method for dyeing PTT carpet continuously
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